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Energy Conservation
Energy Conservation
CONSERVATION
Edited by
Azni Zain Ahmed
ENERGY CONSERVATION
Edited by Azni Zain Ahmed
Energy Conservation
http://dx.doi.org/10.5772/2788
Edited by Azni Zain Ahmed
Contributors
Mikhail Ja. Ivanov, Dujuan Kang, Vivien Mweene Chabalengula, Frackson Mumba, Mohammed
Taih Gatte, Rasim Azeez Kadhim, Akubue Jideofor Anselm, Chong-Hu Wu, A.S. Abdulkareem,
A. Jimoh, A.S. Afolabi, J.O. Odigure, D. Patience, U.C. Odili, Lin Rulong, Cai Wenxuan, Xing
Bingpeng, Ke Xiurong
Published by InTech
Janeza Trdine 9, 51000 Rijeka, Croatia
Copyright 2012 InTech
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which allows users to download, copy and build upon published articles even for commercial
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Notice
Statements and opinions expressed in the chapters are these of the individual contributors and
not necessarily those of the editors or publisher. No responsibility is accepted for the accuracy
of information contained in the published chapters. The publisher assumes no responsibility for
any damage or injury to persons or property arising out of the use of any materials,
instructions, methods or ideas contained in the book.
Publishing Process Manager Daria Nahtigal
Typesetting InTech Prepress, Novi Sad
Cover InTech Design Team
First published October, 2012
Printed in Croatia
A free online edition of this book is available at www.intechopen.com
Additional hard copies can be obtained from [email protected]
Energy Conservation, Edited by Azni Zain Ahmed
p. cm.
ISBN 978-953-51-0829-0
Contents
Preface IX
Section 1 Understanding Energy Conservation 1
Chapter 1 Space Energy 3
Mikhail Ja. Ivanov
Chapter 2 Barotropic and Baroclinic Tidal Energy 57
Dujuan Kang
Chapter 3 Understanding Energy Conservation:
Intersection Between Biological
and Everyday Life Contexts 73
Vivien Mweene Chabalengula and Frackson Mumba
Section 2 Applications of Energy Conservation 93
Chapter 4 Hydro Power 95
Mohammed Taih Gatte and Rasim Azeez Kadhim
Chapter 5 Earth Shelters; A Review of Energy
Conservation Properties in Earth Sheltered Housing 125
Akubue Jideofor Anselm
Chapter 6 Low Energy-Consumption Industrial
Production of Ultra-Fine Spherical Cobalt Powders 149
Chong-Hu Wu
Chapter 7 Production and Characterization
of Biofuel from Non-Edible Oils:
An Alternative Energy Sources to Petrol Diesel 171
A.S. Abdulkareem, A. Jimoh, A.S. Afolabi,
J.O. Odigure and D. Patience
VI Contents
Chapter 8 Production and Characterization of
Biofuel from Refined Groundnut Oil 197
A. Jimoh, A.S. Abdulkareem, A.S. Afolabi,
J.O. Odigure and U.C. Odili
Chapter 9 Optimalization of Extraction Conditions
for Increasing Microalgal Lipid Yield by Using
Accelerated Solvent Extraction Method (ASE) Based
on the Orthogonal Array Design 221
Lin Rulong, Cai Wenxuan, Xing Bingpeng and Ke Xiurong
Preface
The issue of energy conservation has been with us since the seventies and there has
not been a dearth of ideas and increase of knowledge arising from research from
various disciplines ever since. The importance of energy conservation has been on the
increase that has resulted in the need to produce books to introduce new and richer
findings and applications in this field.
This book comprises of nine chapters which cover several disciplines. Each chapter has
been carefully written by leading teams of experts from various parts of the world.
This publication of book has been intended to look deeply into the rudiments of
sources of energy, how energy is transformed from one state into another, from space
to ocean. One chapter describes in vivid detail about space energy, cosmic radiation
and their relation to established thermodynamic laws. The next chapter describes how
energy is collected, stored in the ocean and describes the mechanisms on the energy
transformations and how energy can be used from tidal waves. Another chapter
actually dwells on the importance of education and how the subject should be
approached to make students understand energy and energy conservation better.
The section on applications of energy conservation is very interesting as the contents
are rarely published. A report on the investigations into traditional earth sheltered
dwellings such as sunken earth houses suggests that there are potentials in passive
building insulation which utilizes ground thermal inertia. The techniques of earth
sheltering have not yet become common knowledge in building practice and
architecture, and as such society is unaware of the process or benefits of this type of
building construction. On the contrary, it is well-known that dams are sources of
renewable energy but it is not commonly reported about energy losses that can occur
in the process of transforming kinetic energy to electrical energy. A chapter on
hydropower explains the fundamentals of energy production from dams and how
energy can be conserved through the considerations and design of the turbines and
pipelines where most of the energy is lost from friction.
Although energy conservation plays a vital role in protecting the environment and
optimising the use of energy from conventional fuels, there is of course the
contribution from alternative energy resources. A chapter reports on the production
biodiesel form groundnut oil as an alternative to petrol diesel. We also cannot deny
X Preface
that industrial processes consume the largest percentage of energy in the world. One
chapter provides suggestions on how energy can be conserved in the production of
ultra-fine spherical cobalt powders and another on the optimal extraction of
microalgal lipid. These are certainly innovative ways to contribute towards energy
conservation.
This book does not necessarily cover all the disciplines or the processes that lead to the
reduction of energy consumption in the world. However, the ideas and possibilities
that they represent are just a minute effort to conserve the energy resources on this
planet.
As the Editor of this book, I have found it a pleasure to read each and every chapter
and needless to say it was not easy either. With the enormous responsibilities as a one
of the top academic administrators of a university, it was an uphill task all the time to
complete my duties. I am most honoured and grateful to InTech for appointing me as
the editor of this book. In the process, I too, had learned a lot as through the
responsibilities as editor my knowledge understanding in energy conservation was
enhanced.
I would especially like to thank Ms Daria Nahtigal, the Publishing Process Manager
for pushing me all along to meet the deadlines. Finally, I hope that all the readers
would find this book refreshing, motivating and, most of all, that the book would be of
benefit to students, researchers, professional and practitioners who wish to make this
world a better place.
Azni Zain Ahmed
Head
Centre for Research and Innovation in Sustainable Energy
Universiti Tecknologi MARA
Malaysia
Section 1
Understanding Energy Conservation
Chapter 1
Space Energy
Mikhail Ja. Ivanov
Additional information is available at the end of the chapter
http://dx.doi.org/10.5772/52493
1. Introduction
1.1. Foreword
Our knowledge of the world is guesses and delirium
Omar Khayyam
Vacuum energy. The present chapter considers a possible application of classical mechanics
(more specifically, methods of continuum lightly moving media) for description of the
enigmatic Cosmic Energy (CE). We shall not touch energy processes in the Universe
conditioned by baryon substance conversions when forming and evolving stellar structures
and concentrate on a specific question of modeling dominating CE vacuum that fills free
cosmic space everywhere and even in case of absence of our traditional substance. Herewith
our approach for CE description differs in principal from the virtual energy concept resting
on virtual particles or negative pressure. We consider the CE as a real energy of movement
and interaction of vacuum-filling mass particles, which in divers time were referred to as
ether particles or photons (with finite rest mass) or today particles of hidden Dark Matter
(DM) [1-6].
Dark energy. Here we specially pay attention to widely discussed nowadays a notion of
cosmic Dark Energy (DE) [6-8]. The term "dark energy" appeared in scientific literature in
the end of XX Century and marked the cosmic media filling the whole Universe. DE is
inseparably linked with any space cubic centimeter and according to well-known formula
2
E mc = can be considered a DM equivalent. The first word in terms "dark energy" and
"dark matter" means that this matter form allegedly does not emit and does not absorb
electromagnetic radiation and interacts with usual matter by only gravitationally. The word
"energy" opposes the given media to the structured one consisting of substance particles. DE
density, unlike usual and dark, substance is similar in any space point and its pressure has
negative value. The negative pressure value is the result of the thermodynamic correlation
Energy Conservation 4
E=-pV, which shows the increasing of energy E accompanies by the increasing of
volume V. The DE state equation is written as
2
/ 1 p c ~ [8]. The standard cosmology
model gives DE up to 74% of the total mass-energy quantity of our Met galaxy. The figure
shows the matter distribution in the Universe accepted today in cosmology. The modern
science has carried in consideration the DE and entrusted on it responsibility for the
registered accelerated Universe expansion. Thus we display in detail appropriate
experimental data.
Matter distribution in the Universe
Universe expansion. The last hundred years it is known that Universe expanses. Its possible
accelerated expansion was also discussed and particularly popular this subject became since
1998 when the works [9] were published. Observations of distant Super Nova show that
galaxies scatter from each other with all greater and greater speed. Today this result is
considered without doubts. It was noted as a grandiose achievement of modern physics and
awarded a Nobel Prize for 2011 [10].
We think necessary to emphasize that the conclusion about accelerated Universe expansion
entirely rests on a postulate about constant light speed in vacuum
8
2,998 10 c = m/s and
about impossibility to excess the given speed value by moving bodies. Meanwhile we have
to acknowledge that modern science does not dispose reliable data on measured light speed
in the early hot Universe. If in hot Universe the light speed in vacuum exceeded its known
today value, than the observed accelerated Universe expansion would get a natural trivial
explanation. We again return to its usual (not accelerated) expansion and no necessity to
carry in consideration the hypothesis of DE presence in Universe. Therefore the given fact of
allegedly accelerated should be interpreted as validation of possible light speed dependency
on temperature of cosmic vacuum. Note in this connection some published experimental
data on measured superluminal light propagation.
Superluminal speed. The history of experimental registration of superluminal light
propagation is as old as its prohibition. This phenomenon was thoroughly studied already
in 30-s of last Century. Thus in [11-15], in particular, it was stated that in hollow metallic
Space Energy 5
tubes electromagnetic waves can have superluminal propagation. The effects of
superluminal propagation of laser electromagnetic pulses were open and studied in 60-s in
academician N.G. Basovs laboratory [16,17]. Measured isolated pulses propagation was 6-9-
fold light speed in vacuum. In experiment [18] recorded pulse propagation in inverse
populated cesium vapor was 310-fold light speed in vacuum. During last 20 years such type
experiments [19-21] as well as experiments on superluminal tunneling [22-25] also
registered a notable excess of vacuum light speed. Superluminal propagation of centimeter
radio waves recorded in [26] and discussed in [27, 28].
Review [29] attempts to explain the specified effects from the standard physical theory.
However some published experimental results are rather difficult to interpret in such a way.
Some last empirical data on superluminal effects in hot hollow metal tube are presented in
[30-33]. The mentioned experimental facts of superluminal propagation of electromagnetic
waves and isolated pulses have a principle meaning under building adequate natural
physical theories.
Causality. One of the fundamental tenets of modern physics is the sacred causality principle
stating that no signal can be transmitted faster than light c. It is confirmed that at speeds
higher than c events sequence becomes inverse, the events band allegedly rolls back.
However this widely spread misunderstanding itself rest on a postulate that light speed is a
maximum possible velocity of interactions propagation. Invalidity of such a statement about
violation of the Principle of Causality can be easily shown by the following example. We
consider another similar postulate (sonic postulate) stating that sound speed in a free
atmosphere space is a maximum possible velocity of interactions propagation. Then
supersonic propagation will naturally violate sonic principle of causality. An unambiguous
conclusion: superluminal propagation like supersonic one does not violate the principle of
causality.
God particles. Rather full analysis of the question about Cosmic Energy is impossible
without regarding links with a fundamental question about the God Particle existence
Higgs boson [34] responsible (as someone thinks) for birth of baryon matter mass. Due to
careful last years experiments at the Tevatrone and Large Hadron Collider this question
now is close to its objective decision. To be or not to be of the Higgs boson leading world
physics forums solve today [35-37]. Still we have no positive answer for this question, and a
possible creation of theoretic physics models are under consideration beyond standard
model limits [38] (e.g. models of extra dimension, super symmetry, top quark physics, etc.).
However alongside with the mentioned up-and-coming directions one should not forget
about classic physics models up to limits of ditto time standardized models. Here the typical
example may be the Hidden Mass Boson (HMB) [39, 40], which also as the Higgs boson
might take itself the responsibility for the baryon matter birth.
The chapter materials offered to the Reader is entirely based on the traditional classic
physics. We show the Cosmic Space contains gaseous medium of HMBs with temperature
T=2.725 K and study in detail this medium. The Space Energy presents in our case the kinetic
Energy Conservation 6
energy of HMB particles. We demonstrate the Grand Unified Theory of electromagnetics,
week and strong interactions, electrovalence linkages and antimatter. As additional
experimental confirmations we use the Hooke law, the DulongPetit law, the thermal
expansion law and oth.
1.2. From ancient history
Namely from Leukippus' schooling the era of atomistic in science has started, which
is a theoretical foundation of physics and is continuously developing up to present days.
Therefore we can with full right consider Levkippus as theFather of theoretical physics"
V. Fistul
Theoretic premises of the present chapter are very close to the old Greek philosopher
Leucippus (V century B.C.). In his main work Great space order (Mco, oiokoo,)
Leucippus has developed the atomic matter theory for near Earth and Space. His more
known student Democritus continued to deeply advance the theory and summarized it on
the Micro space order (Miko, oiokoo,). These two original works of materialism
allows to speak of the Leucippus Democritus line in the human through development.
About a century and a half later old Greek philosopher Epicurus seemed to complete the
development of ancient direction of atomic matter theory and publishes a final work On
atoms and vacuum. Their successor poet-philosopher of antic Rome Titus Lucretius
Carus (first half in I century B.C.) brilliantly described this theory in his famous poem
On the Nature of Things (De Rerum Natura). Note specially, the developed theory of
antic atomism was the most successful theory, actually spread the atomism up to the
matter subbaryonic level and presented it as an information bearer for a human
being.
In conclusion we cite a brightest inference of ancient materialism by Lucretius Carus [41]:
In is clear from here that the essence of soul and intellect
Has been created undoubtedly from primary particles petty,
And absence of their gravity does not lessen their essence.
Democritus circa 470 390 B.C. Epicurus circa 341 271 B.C. Lucretius Carus circa 95 55 B.C.
Space Energy 7
1.3. From XVIII-XIX centuries
The ether finest substance filling the whole invisible
world is capable to possess this movement and heat
and also it transfers this movement obtained from
the Sun to our Earth and other planets and heat them, so
the ether is a medium by means of which the bodies
separated from one another transfer heat to each other.
M.V. Lomonosov [42]
The question of space energy and heat nature was thoroughly studied by Russian scientist
M.V. Lomonosov in the middle of XVIII Century. In his original work About the reason
of heat and cold [42] he argues that the heat consists of substance movement and this
movement though not always sensitive but really exists in warm bodies. This movement
is internal, i.e. insensitive particles are moving in warm and hot bodies, and bodies
themselves comprise these particles. Considering the heat (energy) nature in the form of
finest substance particles and ether movement, Lomonosov in ditto time sharply raises an
objection to another interpretation of heat nature in the form of hypothetical heat
generation (phlogiston), when the body heat is tied with heat generation quantity and
heat transportation is connected with heat generation flow from hot bodies to the cold
ones. Lomonosov says: We confirm that the heat cannot be prefixed to concentration of
some fine substance no matter its name. The present chapter demonstrates from
modern scientific positions the fairness of many Lomonosovs conclusions regarding the
heat (energy) nature.
We want to underline that the heat generation concept (phlogiston concept) in spite of
justified critiques has continued to dominate in science for about 100 years. Thus Saudi
Carnot leaning on the heat generation model in his wonderful work Cogitation about fire
propulsive force and about machines capable to develop this force published in Paris, 1824
comes to few basic results of heat theory and formulates a principal idea of heat and work
equivalence. He writes in his later researches: The heat is not that other but propulsive
force or rather movement that changed its shape; it is body particles movement; everywhere
propulsive force disappears at once the heat generates in qualities exactly proportional to
the disappeared propulsive force quantity. Otherwise, always when heat disappears the
propulsive force originates. To present the propulsive force notion later the scientists
started to use the term energy. We give also Carnots formulation of the energy
conservation law: Thus one can say a common expression: the propulsive force exists in the
nature in constant quantity; generally speaking, it is never produced, is never destroyed;
actually it can change its shape, i.e. it generates either one movement type or another, but
never disappears. We find further development of the energy conservation thermodynamic
law in works by Mayer, Joule, and Helmholtz the latter gives its generally accepted
mathematical formula.
Energy Conservation 8
Beginning with R. Clausius and W. Thomson studies in 50-s of XIX Century the heat nature
is finally connected with certain particles movement type. The basic Clausius work
Mechanical heat theory considers light heat as ether fluctuating movement; in bodies
the heat is movement of substance and ether fine particles, and heat quantity is a
criterion of this movement live force. R. Clausius developed the basics of classic
thermodynamics and proposed a convenient form of their presentation as the first and
second beginnings.
W. Thomson in his studies on heat theory and, in particular, in work About heat dynamic
theory also believes that heat is not a substance but a dynamic form of mechanical effect
and certain equivalence should exist between work and heat. In contrast with R. Clausius,
W. Thomson especially pinpoints an idea that the second thermodynamic beginning
expresses the energy dissipation process. Thus, W. Thomson believes, the nature is under
control of the energy dissipation principle. The idea of the Universe heat death is
known follow from this principle.
The second half of XIX Century is marked by outstanding James Clerk Maxwell and Ludwig
Boltzmann works on the theory of thermogasdynamic processes. In review monograph
Substance and movement Maxwell gives the following definitions: The energy is an
ability to conduct work, The heat is an energy type and explains that warm body fine
particles are in a state of quick chaos agitation, i.e. any particle always moves very quickly
and its movement direction changes so fasten that it displaces very small or does not
displace at all from one place to another. This is true, a part, and may be very big part of
warm body energy should be as a kinetic energy type.
In addition to the mentioned citing it is very important for further discussion the Maxwells
weighted velocity wise distribution of similar particles system uniquely determined by
system temperature and particles mass. Presently the formula has a title: the Maxwell-
Boltzmann equilibrium velocity distribution formula. Our work main conclusions in much
degree are based on this distribution.
M. V. Lomonosov (1711-1765) Saudi Carnot (1796-1832) Rudolf Clausius (1822-1888)
Space Energy 9
Principal questions of thermodynamic theory from standpoint of gas kinetic theory are
studied by Ludwig Boltzmann. His Lectures on gas theory [43] begin with words
Already Clausius strongly distinguished the general mechanical heat theory based mainly
on the two theorems, by his example called the elements of heat theory, from the special
theory, which, firstly, certainly believes that heat is a molecular movement and, secondly,
attempts to develop a more accurate interpretation for this movement character. Using
statistic approach Boltzmann analyzes main positions of the mechanical heat theory.
Completing the review of energy theory origins we additionally underline that foundations
of electromagnetism theory are obtained by Maxwell also on the base of ether concept [44].
It is well known, Maxwell in his basic Treaties on electricity and magnetism used a model
of light ether as an invisible fluid. In particular, in the article About Faraday power lines
he writes: Reducing everything to purely mechanical idea of some imaginable fluid
movement I hope to achieve generalization and accuracy and avoid the dangers that occur
at attempts with the help of premature theory to explain phenomena reasons.
Discussion on questions of physics basics, and first all, what actually exists - matter or
energy, unrolled sharply on the edge of XIX and XX centuries. In a bright report On
development of theoretic physics technique in the newest time delivered at a Nature
Scientists Meeting in Munich, September 22nd, 1899 Ludwig Boltzmann considers this
question from the positions of classic atomistic mechanics. Touching electromagnetic
phenomena he, in particular, says: The matter is that alongside with weighted atoms the
existence of special substance made of significantly smaller atoms, namely, light ether been
allowed. In turned out possible to explain nearly all right phenomena, which earlier Newton
referred to do a specific light particles emanation, by lateral ether oscillations. Though some
difficulties remained, for instance, it was unclear why there is complete absence of
longitudinal waves in the light ether, which in all weight bodies both exist and play major
role. Further in that report, expressing care about the approaches of newest energetic
physics being published Boltzmann exclaims: I have remained the last among those who
admitted the old by all their soul; else I am the last who still struggles for this old whenever
William Thomson (1824-1906) James Clark Maxwell (1831-1879) Ludwig Boltzmann (1844-1906)
Energy Conservation 10
possible. I see my vital task as the following: by means of possibly clear and logically
regulated development of the old classic theory results to make if in future not-necessary to
re-discover a lot of good and still suitable things, that, in my opinion, are contained in this
theory, as it repeatedly happened in this history of science. Lets cite as well another
Boltzmanns idea said in the end of that report: Whether once again would the mechanistic
philosophy with the battle, having at last found a simple mechanic model of light ether, at
least would the mechanic models maintain their meanings in future or would a new non-
mechanic model be accepted the best?
1.4. From XX century
Sir, I tell you on the level:
We have strayed, we've lost the trail.
What can WE do...
A.S. Pushkin (1830)
The mechanical philosophy has suffered a major defeat from creation of special and general
theories of relativity. The authors of basics of the special theory of relativity (STR) rested
entirely on the two widely discussed scientific results of that time. The first followed from
unsuccessful experiments on detection of light-bearing ether (famous experiments by
Michelson Morley). A. Poincare, one of the STR authors writes about it in 1895:
Experience has given a lot of facts, which admit the following generalization: it is
impossible to detect absolute matter motion or, more exactly, relative motion of material
matter and ether. All that is possible to do to detect material matter motion relative to
material matter. The principal generalization cited becomes further the first STR postulate.
Below this postulate is given from P. Tolman monograph [45] approved by A. Einstein
himself: It is impossible to detect the uniform progressive motion of a system in free space
or in any hypothetical ether media, which could fill this space. Therefore it is reasonable to
speak only about relative movement of two systems and no sense to mention absolute
motion (for example, absolute system motion relative to the universe ether). From this
viewpoint, there is no necessity in the mechanic ether.
The second scientific result deals with the field of theoretical research of that revolutionary
time. For the first time these linear transformations of space-time coordinates named after
Lorentz were obtained in 1887 by V. Fogth as transformations preserving the invariance of
dAlembert wave equation. In 1900 G. Larmour showed that the Maxwells electrodynamics
equations in free space are also invariant regarding these transformations. Later in 1904 they
also were written by Lorentz and since 1906 by Poincare proposal were named the Lorentz
transformations. Considering peculiarities of the Lorentz transformations Einstein points
out: Velocities of material bodies exceeding speed of light are impossible, that follows from
appearance of the radical
2
1 v in formulas of the particular Lorentz transformation.
Assuming, that at transition to a system moving with v speed the time-space coordinates
changes in accordance with the Lorentz transformations, quite naturally the second STR
Space Energy 11
postulate becomes effective: the speed of light in free space is identical for all observers
regardless relative velocities of a light source and observer. The speed of light c in free
space may now be considered as the maximum allowable speed and, first of all, the
maximum speed of interactions propagation. Unification of the relativity principle and
limit speed of interaction propagation is called the principle of relativity by Einstein (it was
formulated by Einstein in 1905) is contrast with the principle of relativity by Galileo, which
is based upon the infinite velocity of interaction propagation,- read the Field theory
course L.D. Landau and E.M. Lifshitc [46].
Thus the STR erects an insurmountable light barrier for allowable matter motion speeds
and for any weak or strong signals propagation speeds (speeds of information propagation).
In completely rejects the body ether of XIX century. The Einsteins article About the ether
begins with the words: Speaking here about the ether we surely do not mention the
physical ether of mechanic wave theory which obeys the Newton laws and some points of
which have velocity. This theoretic presentation, in my opinion, has completely gone off the
scene with the creation of the STR. Roughly so reads a verdict to the classic physical ether.
The ideas of STR are developed in the General Theory of Relativity (GTR) created by
Einstein in 1906 1915. The physical processes in GTR are described in a curved space-time
system with variable metrics. The curvature of space-time allows to build an interesting
model of gravitational interaction based on similarity between the results obtained in
gravitational field using a uniformly moving reference system and results in absence of a
gravitational flied with an accelerating reference system. This similarity is accepted as the
second GTR postulate and called the equivalence principle. The GTR realizes in full the idea
of relativity of any motion.
Further physics development in the XX century was dominated unconditionally by the GTR
and STR and, naturally, was brightly imposed on the whole modern theoretical physics.
2. Key experimental data
A Rational Being! Turn your eyes to the serene sky.
What a wonderful order is there!
Kozma Prutkov (Russian man of sense, literary person).
2.1. Cosmic microwave background radiation
One of the important achievements of experimental astrophysics of the second half of the
XX century was the discovery of the Cosmic Microwave Background (CMB) radiation. The
existence of this radiation was predicted by George Gamow in 1948. According to his idea of
the Universe origin as a result of the Big Bang, the current radiation appeared at the initial
stages of the Universe development and it was "severed" from the matter spreading this
radiation and so far it has cooled off to a very low temperature. The temperature of CMB
was predicted by Gamov also (accurate within 7 K). In 1955 the post graduent radio
Energy Conservation 12
astronomer T.A. Shmaonov in the Pulkovo Observatory experimentally observed noise
microwave radiation with the absolute value of the effective temperature 43 K. After
Shmaonov had defended his dissertation, he also published the article [47].
In 1966 CMB was registered by the American astronomers A. Penzias and R. Wilson [48]. The
careful researches of the last decades showed that the distribution of the radiated density does
not depend on the direction of its registrations, and that it corresponds to the equilibrium
radiation of a black body with the T=2.725 K. These properties of radiation discuss the
possibility that we dont have the case with transformed radiation of stellar objects but with
the independent substation filling the entire Universe. According to Ja.B. Zeldovich [49] CMB
was sometimes called new ether. This name was given as a result of dipole anisotropy
discovery of CMB at the middle of 70-years [50]. This circumstance allows the introduction of
the absolute cosmological frame of reference in the vicinity of our own Galaxy where the
background radiation is isotropic (accurate within small-scale fluctuations).
Before the discovery of CMB with the final value of the temperature T it was thought that
the temperature in the vacuum of cosmic space is T=0 K and the pressure of the vacuum is
p=0. These values conformed to the properties of carries of electromagnetic radiations
photons with their rest mass m=0, the velocity of their moving in a free space can be equal to
the speed of light in vacuum c=2.99810
8
m/s only, their impulse P and energy E that connect
with each other by the formula E=Pc. The photons do not cooperate with each other, and
their totality behaves as ideal gas (with the adiabatic index =4/3).
However, the discovery of the final temperature of CMB T=2.725 K should cardinally change
the situation. By virtue of the kinetic theory by L. Boltzmann [41] and the dimensional
analysis [51-53] (the - theorem by E. Buckingham [54]) we come to the final values of
pressure and the mass particle in the physics space vacuum
2
, ,
kT
p nkT m
c
=
where k the Boltzmanns constant, n concentration of particles in examining space.
Thereby we introduce with necessarily the ideal gas mass medium to the cosmic space
(physical vacuum). This medium can be identified with the mass photon gas or the Dark
Matter (DM) of the 20th century or it can also be considered as the classic ether of the 19th
century. In the present work for such a medium the particle structure is based and called
Hidden Mass Boson (HMB).
2.2. Dark matter
We shall present the main experimental facts proving existence of Dark Matter (DM), which
were repeatedly described in literature, (see [1-7]).
Astronomer Oort set the problem of possible presence of DM in the Universe in 1932 with
connection to his measurements of motion of stars in the disk of our Galaxy Milky Way. An
unexpected conclusion of his measurements was an essential lack of the aggregate Galaxy
weight for explanation of rotational speeds of the disk. One year later astronomer Zwicky,
Space Energy 13
studying dynamics of the clusters of galaxies, has come to the conclusion, that the observed
weight makes only about 10% of the total mass required for a reasonable explanation of
observations of the total mass in the clusters of galaxies. Special spectroscopic and
radioscopic observations of rotational speed of hundreds of spiral galaxies were executed
later. These observations have shown the essential increase of total mass of galaxies in the
direction of the edge of the stars disk. These facts indicated to presence of the spherical
material halos surrounding the spiral galaxies, which could not be registered in the other
way (i.e. was invisible). Careful observations of elliptic galaxies and clusters of galaxies have
also indicated to the presence of the invisible dark matter gravitationally interacting with
the visible objects of the Universe.
The other experimental confirmation is the hot gaseous congestions. Explanation of their
existence with registered parameters requires presence of DM in quantities noticeably
exceeding the visible matter. We underline, that the empirical fact of the DM existence in
Meta-Galaxy is now conventional.
DM at present time is one of the most intriguing mysteries of the nature. There were
multiple attempts to describe the nature of DM, but no one was successful yet (see [4, 5]). As
it was already noticed, DM (with DE) makes not less than 96% of all matter of our Meta-
Galaxy. A number of theoretical models of DM based on principles of the modern physics
are proposed. Spreading of mass value of the DM particles in different theories reaches 78 to
80 orders: from mass values of
6
10 eV
to
36
10 Kg).
We shall briefly list the main candidates for the DM particles. The main candidates for the
baryonic DM are the Massive Astronomical Compact Halo Objects MACHO. Usually
MACHO includes dwarf stars (white, black or brown dwarfs), planet such as Jupiter,
neutron stars and black holes. The careful analysis of the aggregate contribution of the listed
baryonic objects to the total substance mass of the Universe performed last years has shown
that the DM problem cannot be solved with help of the baryonic matter only. We repeat that
the aggregate estimation of the all baryonic matter in the Universe makes less than 5% of the
total matter.
Non-baryonic DM is usually divided into two main categories: Cold Dark Matter CDM,
which particles moves at subluminal velocities, and Hot Dark Matter HDM, which
particles should move at relativistic velocities, close to that of light in vacuum. The main
candidates for CDM should be Weakly Interacting Massive Particles WIMP with mass of 1
GeV and more. Now intensive searches of such particles with the help of different special
detectors are under way [5-7].
The ultra-light sterile axions with mass in range of
6 3
10 10 eV
are considered as
hypothetical DM particles. Axions were introduced into the theory of elementary particles in
order to explain violation of the invariance in the early Universe [55, 56]. Axions should
Energy Conservation 14
breakdown into two identical photons under action of an external electromagnetic field [56].
With the purpose of registration of such disintegration and confirmation of the axions
existence, the super-sensitive axion detectors are developed now.
Neutrino and anti-neutrino are the characteristic particles of HDM. Their mass, as
candidates for HDM, should be in the range of 10 to 100 eV.
Other candidates for DM are different super-symmetrical particles, which could be formed
at the initial moments of the Universe existence (when it was super-symmetrical and
when all the four interactions were united). Detailed information on all possible
hypothetical DM particles is presented also in the proceedings of the last conferences on
particle physics [35-38].
2.3. Some astrophysics data
Gamma-ray bursts. An actual unsolved problem of astrophysics is the problem of powerful
bursts of gamma radiation, which registration began in the middle of 60s with the help of
special equipment of reconnaissance satellites [57, 58]. Now similar bursts are registered 3 to
5 times a day and are intensively studied [59-62]. An important feature of the gammabursts
is their after-glowing in x-ray and light ranges, which approaches Earth considerably later
than initial bursts do.
The delay time of afterglowing can be more than one year [60, 61]. At the present time
there is no theoretical model, adequate to the phenomena of the gammabursts propagation
to the large cosmological distances, which could explain absence of apparently essential
energy losses of the propagating bursts.
Cosmic rays. Origin of the cosmic rays of ultrahigh energy (more than
20
10 eV ) is a
difficult to explain problem of astrophysics [63-65]. The registered energy level greatly
exceeds the permissible by theory limit of the energy spectrum of particles of the primary
cosmic rays (because of the known effect of interaction with relict photons of Greisen
ZatsepinKuzmin (GZK) [66]). Unanswered questions are both the mechanism of the
charged particles acceleration to the high energy levels and capability of their propagation
to the huge cosmological distances without essential energy losses. The explained problem
is called GZK paradox. Theoretical approaches beyond the framework of the modern
standard models of theoretical physics are proposed (see, for example [35]).
Cosmic jets. The extragalactic superluminal jets propagating from the centers of quasars
and active galaxies remain an astrophysical enigma [67]. Registered during the last years
velocities of propagation of such jets exceed the speed of light in vacuum by 6 to10 times
[6870]. One of the latest publications on this subject informs of the presence of a giant jet of
more than 300 kilo parsec of length (one million light years) at quasar RKS 1127145
containing more than 300 barrels [71].
In the last time during two decades, there is considered also the mentioned earlier
accelerating expansion of the Universe. The accelerating expansion means that the Universe
Space Energy 15
could expand forever until, in the distant future, it is cold and dark. The teams discovery
led to speculation that there is a dark energy that is pushing the Universe apart [9, 10].
Astronomers and physicists have so far failed to discover the nature of this strange,
repulsive force with negative pressure [8].
2.4. Electromagnetic evidences
Sonoluminescence. Sonoluminescence is the emission of short bursts of light from
imploding bubbles in a liquid when excited by sound [72, 73]. Sonoluminescence can occur
when a sound wave of sufficient intensity induces a gaseous cavity within a liquid to
collapse quickly. This cavity may take the form of a pre-existing bubble, or may be
generated through a process known as cavitation. Single bubble sonoluminescence occurs
when an acoustically trapped and periodically driven gas bubble collapses so strongly that
the energy focusing at collapse leads to light emission (Figure 1). Detailed experiments have
demonstrated the unique properties of this system: the spectrum of the emitted light tends
to peak in the ultraviolet and depends strongly on the type of gas dissolved in the liquid;
small amounts of trace noble gases or other impurities can dramatically change the amount
of light emission, which is also affected by small changes in other operating parameters
(mainly forcing pressure, dissolved gas concentration, and liquid temperature). The light
flashes from the bubbles are extremely shortbetween 35 and a few hundred picoseconds
longwith peak intensities of the order of 110 mW. The bubbles are very small when they
emit the light. Transfer of shock wave kinetic energy to light burst energy may be simulated
with help of the conservation law system from the section 4.4 of the chapter.
Figure 1. Sonoluminescence main stages
Displacement current. The proposed in this chapter physical model of vacuum and the
suggested structure of the HMB give very clear interpretation of the Maxwell displacement
current and the Umov-Poynting vector. Firstly, we are reminded of the spread example of
necessity to introduce the displacement current to Amperes law. For instance, a parallel
plate capacitor with circular plates is charged by current I (Figure 2). The magnetic field in
the point at a distance r from the conductor can be calculated by Ampere law
0
2
4 .
S
k
Bds jdA
c
t =
} }
Integrating with respect to the circle we will obtain the magnetic field in the point P
Energy Conservation 16
2
2
,
kI
B
c r
=
where
S
I jdA =
}
is summed current flowing through the surface S. The Amperes law has to
issue for surface S', that is based on the same circle but coming between plates of the
capacitor. By adopting this method the availability of current and electric field between the
plates of the capacitor, the displacement current is introduced to Amperes law has an
additional term
0
2 2
1
4
k E
Bds jdA dA
t
c c
t
c
= +
c
} } }
The last term was introduced by Maxwell (and was named the displacement current). The
physical meaning of the displacement current in our case is the displacement of dipoles of
HMB and their re-orientation between the plates of the capacitor. In vacuum (when
dielectric is absent) availability of the displacement current between the plates of the
capacitor comes to the polarization of real HMB dipoles and we see clean and real physical
interpretation of this current.
Figure 2. The Maxwell displacement current and the Umov-Poynting vector.
Space Energy 17
The Umov-Poynting vector. Now we examine the Umov-Poyting vector of the
electromagnetic energy flux. With changing of electric field E within capacitor, its internal
volume acquires energy. The energy flux is described by the Umov-Poynting vector E B
and has direction from the edges of the plates to inside of the capacitor (Figure 2) from its
surrounding space. As well as the displacement current in our case (availability of the HMB
dipoles) the energy flux of electric field has physical meaning and connects with the moving
(flowing) of dipoles from surrounding to inside.
The propagation of current inside the conductor takes place when the incidence of electric
potential along the conductor and the availability drops electric field E inside and close to
the conductor which in turn is directed alongside the conductor. Availability of the current
induced magnetic field B around the conductor is directed on tangent to the circle around
the wire. The vectors E and B are perpendicular. There is energy that flows to the inside of
the conductor from all sides and which accompanies an energy lost by the conductor as heat.
The classic theory shows that electrons take their energy from outside, which means from
the energy flux of the outside field to the inside of the conductor. Existed HMBs in electric
dipole form are created by the energy flux going to the conductor, which in turn is
processing electric current along it more clearly. The same natural interpretations we get to
known phenomena of inductance and self-inductance.
3. Key theoretical items
And for the rest, summon to judgments true,
Unburied ears and singleness of mind
Withdrawn from cares; lest these my gifts, arranged
For thee with eager service, thou disdain
Before thou comprehendest: since for thee
I prove the supreme law of Gods and sky,
And the primordial germs of things unfold,
Whence Nature all creates, and multiplies
And fosters all, and whither she resolves
Each in the end when each is overthrown.
Titus Lucretius Carus [41]
Theoretical models of the nonlinear dispersion processes considered below are wholly based
on the experimental facts and principles of the Newtonian mechanics. When describing
these processes, the independent variables are time t and three spatial coordinates x, y, z, i.e.
motion of a material medium is supposed in the three-dimensional Euclidean space. Taking
into account fundamentality of concept of time and space and broad discussions of this
problem held in the XX century, we shall briefly consider this and other problems which are
important from the point of view of the present chapter (in particular, concepts of the
subbaryonic dark matter and dark energy, principle of relativity and some other principles).
Energy Conservation 18
3.1. Time
Absolute, true, mathematical time itself and its essence,
without any relation to anything external flows
uniformly and in another way called duration
I. Newton The Beginnings [74]
The time does not exist by itself, but within the subjects,
We all feel it, when something happened in the past,
Whether it happens now, or in the future it will follow
So far, one has never considered the time
Without its relation to the bodies motion or their sweet rest.
Lucretius Carus De Rerum Natura[41]
Absoluteness and one-dimensionality. In the Newtonian mechanics, the basic property of time
is its absoluteness. This property means that time does not depend on the selected reference
system. Any time interval t is the absolute invariant for any nature process and does not
depend on course of the considered processes. It is convenient in many cases to accept a second
as a reference time unit and to define it as a basic unit for the time measurement.
Time is one-dimensional and common always and everywhere.
Homogeneity. Another important property of time is its homogeneity. Homogeneity of time
characterizes its uniform development and supposes equivalence of all moments of time. This
property allows to arbitrary select the zero time reference, i.e. an instant t=0, and reference
interval of the time measurement. It is convenient to study the development of any process
from its initial reference point and to characterize it by the current moment t, measured by the
selected interval (measurement unit). It is also convenient to connect the absolute time with
our Universe and assign the initial reference point to the moment of the Big Bang.
Single directivity. Property of single directivity of time consists in its development in one
direction only forward, i.e. increasing its value. It cannot be turned back to the past. In
other words, there is a so-called arrow of time [75] (from the past to the future). Thus the
principle of causality is fulfilled corollary depends on the reasons, causing that, i.e. the
present order of things depends on the past only and does not depend on the future. We
underline, that in our case the causality principle is fulfilled unconditionally and irrelevant
to any reference value, for example, to the speed of light in vacuum (velocity of propagation
of a signal or disturbances). Within the framework of the Newtonian mechanics, the speed
of light in vacuum is not the maximal possible velocity of the information transfer.
Abstractness and infinity. Property of abstractness of time is perfectly formulated by
Lucretius Carus in the epigraph quoted at the beginning of this paragraph. The property of
infinity speaks about absence of the beginning and end of the time flow.
So, we shall use the absolute, one-dimensional, homogeneous, unidirectional, infinite,
abstract definition of time. Such concept of time lies in the foundation of the Newtonian
Space Energy 19
mechanics. It was widely used at the dawn of the scientific development in the natural
philosophy (Leucipus, Democritus, Epicurus, Lucretius Carus). Transition from the
mathematical abstract time to the physical one is related to selection of the reference
point of counting and interval of time measurement.
3.2. Space
Absolute space by its essence,
Regardless to anything external,
Remains always identical and fixed
I. Newton The Beginnings [74]
There is no end of any side of the Universe,
For otherwise it surely would have the edges;
Nothing can have the edges, obviously, anything, if only
Outside of it there is nothing, that it separates,
That would be visible
Our feeling was, up to monitor it is capable
Also is indifferent, in what you are parts installed
Lucretius Carus De Rerum Natura[41]
Absoluteness, three-dimensionality, isotropy and homogeneity. Rather customary for our
usual life the absolute three-dimensional Euclidean space forms the basis of the Newtonian
classical mechanics. It is isotropic and homogeneous. All points of the space and all
directions are equivalent. These properties of space allow to arbitrary select a point of origin
of three independent Euclidean coordinates x,y,z, (for example, rectangular Cartesian) and
direction of the coordinate axes. It is convenient to combine the coordinate origin of the
absolute space with an initial point in space, where in limit Big Bang was concentrated.
Thus, the problem of selection of direction for the coordinate axes of isotropic absolute space
will not be essential. All other coordinate systems should be considered relative to the
selected unified absolute system.
Abstractness and infinity. Space is abstract and infinite. Similarly to time it does not exist
by itself, but in subjects we feel it. Space is infinite in all directions. Similar to the time
variable, the transition from the mathematical abstract space to the physical one
consists in selection of a system of spatial coordinates and unit of length measurement.
Invariant interval. The main geometrical invariant when transiting from the absolute
system of Cartesian coordinates to another Cartesian system will be value
2 2 2 2
. s x y z A = A + A + A
which uniquely determinates distance s A between two points in space. Thus transition
from some coordinate system to another one is carried out at fixed time, when location of
points in space is fixed.
Energy Conservation 20
The basic result of brief consideration of concepts of time and space is the following. All
natural processes under investigation are characterized by four independent variables: by
absolute time t and three absolute Euclidean coordinates x,y,z. When transiting between two
coordinate systems, the invariant values are the time interval t A between two events at
fixed point and the spatial interval s A between two points in space at a fixed moment of
time. Point of origin of the absolute time and origin of the absolute system of spatial
coordinates and their directions one can choose arbitrary, basing upon convenience of
studying of physical process. As we already noticed, in case of our Meta-Galaxy (visible
Universe), it is convenient to consider the absolute coordinate system with the time and
spatial coordinates origin located at the initial point of Big Bang.
Experimental data. We shall discuss some experimental confirmations of the Euclidean
properties and of three-dimensionality of our space. The last careful experiments on small-
scale fluctuations of the relict microwave radiation have shown its isotropy with precision
up to
4
10
=
and allows an assessment of the "critical" pressure value
2 9
0 0 0
10 Pa. p c
=
In the case of an ideal "photon" gas with adiabatic constant 4 / 3 k = the speed of
perturbations is defined as
2
0 0 0
/ c p k =
and then we get
9
0
1.4 10 p
= Pa. It should be emphasized that this positive value
0
p can be
interpreted as "critical" pressure of the Universe, determined by means of dimensional analysis
in terms of its critical density
0
. We specifically focus on this fact to point out a fundamental
difference from the negative pressure of the Universe [8], which is associated with the
phantom dark energy that may influence the effect of "accelerating" expansion of the Universe.
A natural explanation for the apparent accelerating expansion of the Universe and a few other
important items follow from the consideration of the dimensionless parameter t2 in the form
Space Energy 25
2
2
1
kT
mc
t =
leading to the estimation of the particle mass
0
m for the media with the temperature
0
T and
the disturbance propagation velocity
0
c
40 0
0
2
0
4.25 10 kg.
kT
m
c
=
An important conclusion of the analysis t2 is directly proportional of the velocity
0
c to the
square root of temperature
0
c ~
0
T . In this connection we would like to get two remarks.
The first is the possibility of a superluminal speed for disturbances in physical vacuum by
T>T0. In our case the limitation on week propagation perturbations velocity is withdraw and
the superluminal motion (without violation of the causality principle) is allowed. Here
relevantly one gives the analogy with the classic gas dynamics, which allows the motion
with supercritical (supersonic) velocities. The second remark is concerned the apparent
accelerating expansion of the Universe. The Universe in the early time periods was hotter,
had a higher temperature
0
T and therefore higher value
0
c . This fact naturally explains the
observed luminosity week effect of distant supernovae.
It should be noted that the combination of dimensionless parameters t1 and t2 leads to a
state equation of an ideal gas. We write the dimensionless parameter
1
3
2
1,
p
nkT
t
t
t
= =
where n=/m - the concentration of particles.
A more accurate assessment for m0 [78-80] gives
40
0
5.6 10 kg. m
=
Further there is based this particle structure as a classic dipole with ultra-elementary charge
near q0=10
-28
C. Hence we can consider in detail a new complex elementary particle - Hidden
Mass Boson (HMB). Dimensional analysis in the presence of a characteristic charge allows
getting two character values: frequency (similar as Langmuir frequency in plasma) and
Debye radius of screening. The last radius plays the key role in our study.
The dimensional analysis will be conducted, relying additionally on two parameters.
Parameter t4 written as
4
2
1
G
t
e
=
allows us to introduce the characteristic gravitational frequency
0
e , the characteristic time
period
0 0
1 / t e = and the characteristic linear dimension
0 0 0
L c t = of our Universe
Energy Conservation 26
18
0 0
0.82 10 1 / G s e
=
The value of the gravitational frequency is an analog of the plasma frequency, which
characterizes the electric displacement of the negative charge from a positively charged
layer. The exact value
0
e is written (by an analogy with the definition of the plasma
frequency) with a coefficient of proportionality 4t , i.e.
0 0
4 G e t = .
We also consider the dimensionless fifth parameter
5
1
hc
kTl
t =
allowing an assessment of the characteristic length
0
l ~
0
0
hc
kT
= 5.310
-3
m. This quantity can
be interpreted as estimation of the mean free path of particles for the physical vacuum,
which has temperature
0
T .
4.2. Elements of thermodynamics and statistical mechanics
An interesting result of dimensional analysis is the presence of particles with mass
0
m in a
free radiating space (the physical vacuum) with the equilibrium temperature
0
T and the
disturbance velocity
0
. The zero law of thermodynamics allows introducing a temperature
as the state parameter. The temperature T0=2.725K characterizes of cosmic background
microwave equilibrium radiation state. By using a simple gas kinetic approach we can find
the refined value of the mass of these particles. The averaged kinetic energy of random
motion of particles is
2
2 0 0
0 0 0 0
0
3 3 9
,
2 2 2 8
av
m v R T
E kT m m c
m N
= = = =
where the /
A
k R N = Boltzmann constant,
R - the universal gas constant,
A
N - the
Avogadro's number. From this relation we obtain for HMB
40 4 0
0
2
0
4
5.6 10 kg 3 10 eV.
3
kT
m
c
= = ~
We calculate the gas constant
0
/
A
R R m N = and specific heat capacity
v
c and
p
c in the
assumption of ideal gas with adiabatic index k=4/3:
17 17 17
0
0.25 10 J / kg K, 0.75 10 J / kg K, 1 10 J / kg K.
v p v
k
R c c c R
m
= = = = + =
Further, following the traditional thermodynamics of ideal gas for radiation medium, we
can write the classical state equation
Space Energy 27
p RT =
or
( 1) , p e k =
where
v
e c T = - the specific internal energy.
An important next step is to postulate the structure of radiation particles, which allows
explaining the large number of effects and phenomena observed in the physical vacuum.
Following [79-80], we consider a whole electrically neutral particle in the form of a dipole
consisting of two parts with positive and negative charge equaled to about 510
-29
Coulomb.
Thus, we actually introduce the new mass medium of bosons - Hidden Mass Boson (HMB)
and can apply to its analysis well developed methods of statistical mechanics and
thermodynamics.
Let us explain in more detail, why the mass particle radiation of the physical vacuum is
taken in our analysis in the form of the dipole, called hereafter by the hidden mass boson.
First, in this case the issue of physical vacuum polarization is extremely clear. In an external
electric field orientation of the HMBs takes on power lines of the electric field, partly
compensating for the external field. Thus, we obtain a clear physical interpretation of the
Maxwell's displacement current in free space. Further, the energy flux vector of the
electromagnetic field - Umov Pointing vector indicates the direction of the HMB
polarization under the influence of an external electromagnetic field. In particular, when
charging of the capacitor without insulator between the plates HMBs are moving from outer
space in between the capacitor plate space, providing in this case, the displacement current.
Another important process of electron-positron pair birth in the physical vacuum in the
collision of two sufficiently intense electromagnetic pulse [81] should be interpreted as a
break in a certain (sufficiently large) number of dipoles - HMB followed by concentration of
their parts of the same sign of charge at the centers of the electron and positron under the
influence of forces including non-electromagnetic nature (e.g., gas dynamics, gravity, etc.).
When implementing this scenario, the HMBs will determine the mass of the birth of
baryonic matter in the physical vacuum.
Substantiated to some extent chosen postulated HMB structure, we proceed to the methods
of statistical mechanics. We consider the important question of the consistency of our work
findings to well-known basics and conclusions of statistical physics and thermodynamics of
a boson gas and its special case - a photon gas with zero rest mass of photons. Below we
demonstrate the absence of such contradictions.
First of all, we write the state equation for gases obeying Bose statistics and Fermi statistics.
Here, the dimensionless parameter can be written [82, 83]
3 0
5/ 2
1
1 ...,
2
p
nkT
t = = +
Energy Conservation 28
where the signs , respectively, for the Bose and Fermi gases, as well
1 3/ 2 3
0
(2 ) / mkT h n t
=
- the statistical sum per particle. The second and higher terms in the right side of the above
formula are quantum statistical origin. This series expansion is valid for values 0<1 or to
values n<
3/ 2 3
(2 ) / mkT h t . The magnitude
1/ 2
/ (2 ) h mkT t is the length of the thermal de
Broglie wavelength, and the value
1/ 2
/ (3 ) h mkT corresponds to the thermal energy of the
particle 3/2kT. Thus the Bose statistics in the usual manner is applied to the entered us with
dimensional analysis and thermodynamics of the HMB gas. For future study the
condensation state of the HMB gas on the lowest temperature and high pressure is also very
important item.
As for the well-known theory of blackbody radiation, in our approximation it requires some
revision, which consists in passing from the linearized formulation of the problem to a fully
nonlinear formulation. The essence of this transition can be clearly illustrated by the
linearized theory of acoustics and the original theory of the nonlinear gas dynamics. It
seems very clear that in a limited gas volume it is possible to describe the its state in the
acoustic approximation using the equation for the acoustic pressure perturbation
2
2
2 2
1
0
p
p
c t
c
V =
c
Based on this description, we can then determine an acoustic sound radiation from a closed
cavity and the radiation field in the outer vicinity of the limit volume. In this description one
can calculate the acoustic field in a gas without going into details of what the gas medium
consists of a mass of individual particles. However, to calculate the real total pressure in the
limited volume the initial nonlinear laws of gas dynamics are required (of them will be
discussed in the section 4.4).
A similar situation occurs with the thermal radiation of a blackbody. Currently, in the
approximation of massless photon equilibrium radiation field is described by the linear
wave equation [82]
2
2
2 2
1
0.
E
E
c t
c
V =
c
The radiation field is represented by a set of simple harmonic oscillators with discrete
spectrum of energy. As a result of the energy spectrum of equilibrium radiation gives the
Planck formula
3
3
8 1
1
h
kT
h
U
c
e
v
v
t v
=
Calculations using this formula are in full agreement with the experimental far field
radiation, where the linearized theory actually works (as in acoustics case). However, in the
Space Energy 29
case of massive bosons radiation the study of the thermal process in limited volume should
be with help of nonlinear formulation, which we detail below.
To conclude this section we emphasize that known values p0 and 0 characterize the state of
the photon gas in the physical vacuum of space (in the vicinity of the Earth and solar
system) with the measured temperature CMB T0 = 2,725 K. The pressure p0 is the direct
pressure of the HMBs medium in the region (source) at T0. This value differs on a factor
c0=310
8
m / s from the linearized values in a far field, which is calculated by methods of
classical electrodynamics. It should specify the complete analogy with the usual gaseous
medium in which acoustic pressure away from the noise source is different from the
pressure at the source (this difference is also characterized by a factor containing the
magnitude of the velocity of disturbance propagation, in this case - the sound speed c).
Further consideration of the influence of thermal radiation effects environment will be
carried out within the framework of two-component model of the emitting gas with the
mass of the photon component [84].
4.3. Modified Maxwell equations in free space
In the medium of physical vacuum being examined the longitudinal and transverse waves
will propagate in the electromagnetic field. The system of linear equations, describing the
propagation of electromagnetic disturbances can be written in the form [40]
0,
0,
0,
0.
e
m
e
m
c rot c gradq
t
c rot c gradq
t
q
c div
t
q
c div
t
c
+ =
c
c
+ + =
c
c
+ =
c
c
+ =
c
E
H
H
E
E
H
With the purpose of longitudinal waves modeling into tradition system of electrodynamics
equations of a free space, the scalar field
e
q and
m
q were introduced and that represents the
density of force lines of electric and magnetic field. The first term in the first equation of the
system is a time change of E and the displacement current in vacuum.
The system describes the propagation of all parameters of disturbances with the same speed
c. It is easy to prove, differentiating the first two equations with respect to t:
2
2 2
2
2
2 2
2
0,
0,
E
c rot rotE c grad divE
t
H
c rot rotH c grad divH
t
c
+ =
c
c
+ =
c
that, by using the formula of vector analysis
Energy Conservation 30
A grad divA rot rotA A =
leads to the waves equations for the changes E and H
2 2
2 2
2 2
0, 0.
E H
c E c H
t t
c c
A = A =
c c
The changes of scalar field qe and qm , as well as scalar and vector potentials of E and H can
be also lead to the wave equations.
The system of linear equations describes the propagation with equal velocities both the
longitudinal waves (the wave of compression and rarefaction) and the transverse wave
(share wave) in a homogeneous isotropic space. At the same time, the modeling of
longitudinal wave is provided by the introduction additionally of the scalar fields qe and qm
to the system Maxwell equations. In this connection, we can call the scalar fields qe and qm as
fields of density (force lines), connecting with fields E and H. In principle, it is not difficult
to examine the case when propagation velocities of longitudinal and transverse waves in the
electromagnetic field are different.
4.4. Conservation laws for two component gaseous medium
Here is a complete system of conservation laws for two component model of gas-like
environment, taking into account the HMB medium (radiation) component. All used
parameters will be denoted in the traditional way. Attributing them to the corresponding
indices: g - for the gas component, f - for the radiation component (e.g. density
g
and
f
).
The total value of the density, pressure and internal energy will be denoted without an
index.
The laws of conservation of mass, momentum and energy in the divergence form for each
component have the form [84]
( ) ,
( ) ,
( ( )) ,
( ( )) ,
( ) ( ) ( ) ,
( ) (
g
g g g
f
f f f
g g
g g g g g
f f
f f f f f
g g
g g g g g g g fg f g g
f f
f f f f f f
div V q
t
div V q
t
V
div V V n grad p r
t
V
div V V n grad p r
t
e
div e V p divV div K gradT c T T Q
t
e
div e V p divV div K gr
t
c
+ =
c
c
+ =
c
c
+ + =
c
c
+ + =
c
c
+ + = + +
c
c
+ + =
c
) ( )
f fg g f f
adT c T T Q + +
(1)
Space Energy 31
This system of equations is written for the thermal conductivity of the gas and radiation
components (the first terms on the right hand side,
g
K and
f
K - the thermal diffusivity of
the gas and radiation components, respectively). The second terms on the right sides of two
last equations characterize the energy exchange between the gas and radiation components.
The last terms,
g
Q and
f
Q are supplementary sources of energy, taking into account the
availability of additional channels of energy exchange (e.g., in the case of registration of
chemical reactions, etc.). The system (1) is closed by equations of state for the gas and
radiation components. Using this set, one can give a natural interpretation of the growth of
entropy in compression shocks, where a part of the kinetic energy of the gaseous component
in the shock turns into heat. When the velocity Vg drastically decreases, a part of the energy
from polarized molecule space goes into the radiation component and this part of energy is
dissipated due to heat conduction.
Of course, a solution of this system in general form involves considerable difficulties,
because we need to specify the value of the exchange heat coefficient cfg between the phases.
Substantial simplification can be achieved by considering the approximation of one
velocity and one temperature movement phase in the presence of a thermodynamically
equilibrium
Vg=Vf=V ; Tg=Tf=T .
We also assume that there are no external sources of mass and momentum in this region of
flow and mass transfer between phases:
qg=qf=0 ; rg=rf=0.
Then, following [85, 86], we represent the continuity equation of each phase in the form
1
0,
g
g
d
divV
dt
+ =
1
0
f
f
d
divV
dt
+ =
or
ln 0.
f
g
d
dt
| |
| =
|
\ .
The last equality says the preservation of values
o=f/g (2)
along the stream lines, and if we assume that the initial time the density ratio is constant and
independent of the coordinates, the equation (2) is valid at any point of considered medium.
Energy Conservation 32
We write total conservation laws for both components of the medium. Adding first two and
second two equations in the system (1) we obtain, taking into account our assumptions,
usual equations of a continuity and a motion for one-component medium
( ) 0,
( ( )) 0 .
div V
t
V
div V V n grad p
t
c
+ =
c
c
+ + =
c
Slightly change the total energy equation. Adding the last two equations in (1) we obtain
( ) ( )
,
, .
vg g vf f vg g vf f
g g f f g f
c c T div c c T pdivV divW Q
t
W K gradT K gradT Q Q Q
c
( (
+ + + + = +
c
= + = +
In order to give the energy equation the usual form, we transform the expression
,
vg g vf f
N c c = +
as
( ) ( ) ( )
( ) ( ) ( )
(1 ( ) / ( )) / (1 ) 1 1 / 1 / ) ,
1 1 / 1 / ) / (1 ), / .
vg g vf f vg g vg g f f g v
v vg g f f g p v
N c c c c k k p p
c k k p p k c c
o
o
= + = + + =
= + + =
Recall that, according to (2) o=f/g, constant along streamlines. Consequently, when Tf=Tg ,
the ratio pf/pg is constant along streamlines.
Similarly, we transform the equation of state for the total system
( )
, 1 / / (1 ).
g f g
p RrT R R p p a = = + +
The energy equation with right term -divS, where the radiation flux S=oT
4
, is often used in
the simulation of the radiate flows. For further analysis with using of this approximation we
obtain the following system, describing the equilibrium one velocity flow in the presence of
radiation effects
4
( ) 0,
( ( )) 0 ,
,
T.
v v
div V
t
V
div V V n grad p
t
c T divc T pdivV div T
t
p R
c
+ =
c
c
+ + =
c
c
+ + =
c
=
Obviously, when f=0 we obtain the ordinary system of gas dynamics equations for one
component radiation medium. Further we present some examples of our model applications.
Space Energy 33
5. Space energy & grand unified theory
Space Energy is conserving,
Space Entropy is growing.
E. Fermi
A classical unified theory of electromagnetic, weak and strong interaction, electrovalence
linkages and antimatter is built coming from our Space Energy simulation. The theory bases
on Hidden Mass Boson in form of a classic dipole and the Debye length of polarized spaces.
These items are the background of our Grand Unified Theory (GUT).
5.1. Debye spheres of electron and proton the background of GUT
"The electron polarizes vacuum, allegedly attracts to itself virtual positrons, and repulses
virtual electrons". So, in particular, the vacuum polarization phenomena are described in
monograph [89]. In full correspondence with similar experimentally confirmed polarization
of near electron space is found the stated below mathematical model of electron and proton
structure. Here we shall imply only under "virtual" electron and positron a real polarized
gaseous structure of DM dipole particles (HMBs), from which, as already noted, electron-
positron pairs might be generated.
Within the framework of considered approximation one can formulate specific equation
system similar the gas dynamics model with electric charge presence, as the two fluid
hydrodynamic plasma model. For steady state from mentioned models we can lightly
derive equations, describing particle electricity potential and concentration distribution in
polarized Debye spaces of electron, positron, proton and anti-proton.
First of all we would like to obtain the estimation of Debye spheres for electron. A Debye
sphere is a volume of influence, outside of which charges are sufficiently screened. In out
simulation a Debye sphere is formed with a pressure field presence of HMB gaseous
medium. For steady state a two fluid hydrodynamic model [90, 91] may be expressed by
equation system (in the SI units)
0
1
,
4
4 ( ),
,
p e
n m m
e n n
p n kT
tc
t
+
V
= V
A =
=
(3)
where , p n
- pressure and concentration of positive and negative of HMB components,
which have the same temperature T, e elementary charge of HMB dipoles. From (3) the
equation of electric potential for polarized space in non-dimensional form is written in
rather simple form
2
2 . D sh A = (4)
Energy Conservation 34
Here potential is referred to its value
0 0
4 T tc = ,
2
0 0
( / ) D sqrt kT q n c = - the Debye radius
(length),
0
n - typical HMB boundary concentration. For concentration of HMB particle
charge component in polarized space we have from (3) the Boltzmann distribution (in non-
dimensional form)
, 0
exp( ) n n
+
=
The Debye length for electron in HMB medium can be calculated using its mass me=9.110
-
31
kg, charge qe=1.610
-19
C and Comptons length e=2.4310
-12
m. The effective electron volume,
which contains the most part of its mass, may be estimated as
Ve = 4/3 e
3
= 0.60110
-34
m
3
.
Our great assumption is the distribution of whole electron mass between the point center
(with the smallest point radius near 10
-17
-10
-18
m, where the whole electron charge is
concentrated) and other volume Ve. Here we assume that the electron mass is dividing near
half. When HMB averaged concentration ne in this volume is
ne = (me/2)/Ve/m = 1.3510
43
1/m
3
.
Further we provide the estimation of HMB dipole charge q. The number of charge particles
in the electron center Ne=(me/2)/(m/2)=1.6210
9
and q=qe/Ne=0.9910
-28
C. Now we can calculate
the Debye electron length of charge screening (by T=2.725K)
De = sqrt(0kT/q
2
/ne) = 0.510
-10
m.
In the spherical symmetric case with single spatial coordinate-radius r we come from (4) to
relationship
2
2
2
2
e
D d d
r sh
dr dr
r
| |
=
|
\ .
We shall bring typical solutions of the last equation for polarized electron space (Figure 4).
A principal important particularity of distribution presented is potential pit and barrier on
external border of polarized space with distribution ( ) r break. Herewith an induced
negative electric charge is concentrated on external border, induced by charged electron core
during polarizations of its "fur coat". The results presented are valid due to charge
symmetry also for description of polarized positron space structure (when changing
potential sign on opposite). The scheme of polarized electron space is shown on Figure 5.
Now consider possible building on the same principles of proton and antiproton model. In
analogy with electron we suppose that the entire positive proton charge is concentrated in
its center, having an estimated size, like electron core size of order
17
10
m. This central
nucleus is spherical "droplet" surrounded polarized by HMB in "fluid" aggregate condition.
The droplet size defines a typical known proton nuclear size (about
15
0.8 10
m), where
Space Energy 35
practically its entire mass concentrates. The concentration of HMB in the fluid droplet is
near 10
57
and the Debye screening radius near 0.810
-15
m. The HMB fluid droplet provides
the effective Debye screening and plays the key role in week and strong interactions.
Around proton nuclear droplet there is polarized spherical HMB space in gaseous aggregate
condition, similar to polarized positron space. Modeling structure of two-layer polarized
proton space is executed by integrating equation (4) for electric potential with the use of
different state equations (for liquid and gaseous HMB phases). Examples of similar solutions
by nature repeat solutions shown on Figure 4. And again basically important here is the
presence of two potential pits and two barriers at
15
0.8 10 r
~ m and
11
0
5 10
e
r D
= ~ m.
The structure built of proton with partial screening of its charge by two-layer polarized
space is steady. Due to charge symmetry the antiproton structure repeats proton structure
(with corresponding change of potential sign and others). The scheme of polarized proton
space is shown on Figure 6.
Figure 4. Potential distribution in electron screening space for two D
The model of hydrogen atom consists of proton with concentrated in its center positive
charge and two-layer HMB polarized space in fluid (up to 0.810
-15
m) and gaseous
aggregate conditions and having an electron situated in steady stationary state on polarized
space external surface (r0=De=0.510
-10
). Herewith for ensuring electron stationary condition
in atom there is no need to introduce additional quantum postulates. This condition is
provided by potential distribution in the electron and proton models built. The scheme of
polarized hydrogen atom space is shown on Figure 7. The potential distribution in the
hydrogen atom is present on Figure 8.
Energy Conservation 36
Figure 5. Scheme of electron screening space
5.2. Physical model of van der Waals polarized atom spheres
The presence of real existing polarized atom space and their forms close to spherical (van
der Waals spheres as Debye screened spheres) is validated by methods of crystal-chemistry
and scanning probe microscopy. By means of tunnel microscope needle one can manipulate
separate spherical atoms, move them on surfaces, build 3D figures, etc. Atom shape
presentation as van der Waals spheres is now broadly used method when studying
substance physical-chemical properties.
The previous section offers models of polarized screened spaces partly shielding central
concentrated electrical charges that enable demonstrative physical interpretation of van der
Waals atom spheres. These spheres are in essence external borders of polarized spaces filled
with HMB dipoles Coulomb interaction bound. On such spherical borders with local
concentrated induced charges might be stationary placed concentrated charges of another
sign (example: hydrogen atom from article previous paragraph).
Space Energy 37
Figure 6. Scheme of proton screening two layer space
Figure 7. Scheme of hydrogen atom
Energy Conservation 38
Figure 8. Numerical solution for potential distribution inside hydrogen atom
Possible stationary steady electron position on van der Waals spheres brings about a model
of atom electronic shell with STationary ELectron (STEL models). Electronic shells of
spherical shape are equidistant to nucleus centre at distances accordingly
0 0 0 0
1 , 2 , 3 , 4 r r r r , etc.
(natural row coefficients 1, 2, 3, 4 show, as accepted, main quantum number). The first
shell area
2
0
4r is fully occupied by 2 stationary electrons; they rather tightly cover nearly
whole area by their own polarized spaces. The following three shells area
( )
2
0
4 4r ,
( )
2
0
9 4r
and
( )
2
0
16 4r can be occupied by less 8, 18, and 32 stationary electrons (double square of
main quantum number); also tightly covering by their own polarized spaces nearly whole
disposable area of corresponding shell. The rule stated defines maximum possible electrons
number on any electronic shell (its "thick packing"), however electrons number on external
shells at once may not reach its maximum value.
Number of ordinal atom element increasing and its nucleus positive charge growing under
action of increasing Coulomb forces, the electron shells compress (
0
r decreases) that fully
complies with experimental data on atom sizes of different chemical elements. Heat
expansion of electronic shells (including external van der Waals spheres) on linear law is
described by corresponding solutions change of equation (4) for polarized atom space when
Space Energy 39
changing Debye radius
2 1/ 2
0 0
( / ) D kT n q c = ~T (since typical gaseous HMB concentration
0
n at similar pressure
0
p is inversely proportional to temperature T).
5.3. STEL model for atoms and molecules
Let us give some examples of typical atomic structures within the framework of STationary
ELectron (STEL) model. Begin with helium atom and its first electronic shell filled by two
electrons. There are two protons and two neutrons in the center of helium atom. On surfaces
of first polarized space helium nucleus border (
15
~ 10 r
m) there are two electrons in
steady state due to total potential distribution. The DM polarized space in gaseous condition
is situated around nucleus on the space external shell (
10
~ 0.5 10 r
m) with two electrons in
steady state. This first electronic shell is tightly "filled" due to the described structures of
electron polarized space (also
10
~ 0.5 10 r
m). Each electron occupies about half spherical
shell around helium atom.
The next is a carbon atom. Its external shell has 4 electrons located in tetrahedral tops
(traditional direction of valence links, Figure 9). Oxygen atom on external shell contains 6
electrons. The least total potential energy of these electrons is provided by their location in
two triangles tops in parallel planes and turned to each other by angle 60 (so called triangle
anti-prism, Figure 9).
Figure 9. Structures for carbon, oxygen, and neon atoms
An inert gas neon atom has on external shell 8 electrons. The least total potential energy of
these electrons forms at their location in square tops turned by angle 45 (square anti-prism,
Figure 9). Similar structure to carbon, oxygen, and neon atoms is for atoms of silicon,
sulphur, and argon accordingly with the same location of 4, 6, and 8 electrons on the third
external shell. One can uncomplicated similar way reproduce stationary electron location on
completely filled third shell with 18 electrons of 4 period (5 rows) elements and fourth shell
with 32 electrons of 6 period elements of the Mendeleyev table.
The illustrated application of STEL model for electron shells description in some features
repeats the known Lewis octets. An important novelty to model STEL is electrons location in
anti-prism tops (for oxygen, neon, sulphur, and argon) providing minimum value of total
potential energy of external electrons.
Energy Conservation 40
Existence of DM polarized spaces of electron, proton, and atomic nucleus allows description
from general positions through Coulomb interaction of any available molecular linkages as
stationary deterministic structures of shell electrons and nucleus. Here we also use the
model STEL. The simplest hydrogen 2 molecule presents a 2D quadrangle, in opposite tops
of which there are two protons and two electrons (Figure 10). These perimeter concentrated
charges are located at distances about Debye radius and partly shielded by HMB polarized
space. Potential distribution in polarized hydrogen molecule space might also be found by
integrating equation (4). Here the covalence link presents a pair of stationary electrons (not
moving on orbits).
Figure 10. Structures for H2, O2 and CO2 molecules
For geometric presentation and physical description of molecular links with participation of
elements of second and third periods of Mendeleyev table we return to modified Lewis
cubic structures and his electron octets. Instead of perfect cubes with electrons in their tops
we have square anti-prisms. Bring some typical examples. In asymmetrical water molecule
each hydrogen atom is connected by covalence link (pair of socialized electrons) with
oxygen atom in neighboring tops of square anti-prism.
Oxygen molecule is united by double covalence link. We have here on the second orbital
shells of each atom electron octets in anti-prism tops (Figure 10 ). An example of "twisted"
molecule with double covalence link serves the molecule of carbon dioxide (Figure 10).
Similar geometric models with square anti-prism structure (electron octets) and covalence
links are typical for carbon compounds. Show, for example, saturated hydrocarbon with
filled octet of the electronic shell - methane (Figure 11). Compounds, similar to carbon, of
third period silicon element with four valency electrons on the following third electronic
shell are also comfortable to present in the form of geometric models with square anti-
prisms; with the only difference - in covalence links participate electrons of silicon third
external electronic shell.
Within the framework of STEL model it is natural ("classical") way to represent models of
hydrogen links, when on the first, nearest to proton (hydrogen ion) shell are stationary
localized two electrons simultaneously belonging to two negative ions. For instance,
hydrogen difluoride
2
HF
0
p
g
0
k +
H
(
H
H
u) +
z
_
V
u
z
_
, (1)
t
+u =
H
(
H
H
) +
z
_
z
_
, (2)
u = 0 , (3)
where u = (u, v, w) is the velocity vector and is the Earths angular velocity vector.
and , in units of m
2
s
1
, are the eddy viscosity and eddy diffusivity, respectively. ( )
H
and
( )
V
are the horizontal and vertical components of a variable or operator. The total density
is given by =
0
+
b
+
, where
0
is the constant reference density,
b
is the background
density, and
is the perturbation density due to wave motions. The pressure is split into its
hydrostatic (p
h
) and nonhydrostatic (q) parts with p = p
h
+ q, where the hydrostatic pressure
can be further decomposed with p
h
= p
0
+ p
b
+ p
. Accordingly,
the kinetic energy density, in units of J m
3
, is decomposed as
E
k
=
1
2
0
_
U
2
+ V
2
_
. .
E
k0
+
1
2
0
_
u
2
+ v
2
+ w
2
_
. .
E
k
+
0
_
Uu
+ Vv
_
. .
E
k0
, (4)
where E
k0
is the barotropic horizontal kinetic energy density, E
k
is the baroclinic kinetic energy
density, and E
k0
is the cross term which vanishes upon depth-integration. Following Gill
(1982), the perturbation potential energy due to surface elevation, in units of J m
2
, is given
by
E
p0
=
1
2
0
g
2
, (5)
in which is the free surface elevation. The available potential energy density, in units of
J m
3
, is dened as
E
p
=
_
z
z
g
_
b
(z) +
(z)
b
(z
dz
, (6)
59 Barotropic and Baroclinic Tidal Energy
4 Energy Conservation
where is the vertical displacement of a uid particle due to wave motions. This denition
is an exact expression of the local APE because it computes the true active potential energy
between the perturbed and unperturbed density proles [12, 14].
Applying the variable decompositions and the boundary conditions, we obtain the
depth-integrated barotropic and baroclinic energy equations as
t
_
E
k0
+ E
p0
_
+
H
F
0
= C
0
D
0
, (7)
t
_
E
k
+ E
p
_
+
H
F
= C
, (8)
where the depth-integrated barotropic and baroclinic energy ux terms, with the small
unclosed terms neglected, are given by
F
0
= U
H
E
k0
. .
Advection
+U
H
H
0
g +U
H
p
+U
H
q
. .
Pressure work
H
E
k0
. .
Diffusion
, (9)
F
= u
H
E
k
+u
H
E
k0
+u
H
E
p
. .
Advection
+u
H
p
+u
H
q
. .
Pressure work
H
E
H
E
p
. .
Diffusion
, (10)
in which the contributions from energy advection, pressure work, and diffusion have been
labeled. The denitions of the barotropic-to-baroclinic conversion rate (C), the dissipation
rates (
0
and
F
0
_
=
C
_
0
+ D
0
, (11)
1
T
E
+
H
_
F
_
=
C
_
+ D
_
, (12)
where =
1
T
_
t+T
t
() d is the time-average of a quantity over a time interval T. For a
periodic system with period T, E
0
and E
F
0
_
term represents the total barotropic energy that is
available for conversion to baroclinic energy,
C
_
represents the portion of the barotropic
energy that is converted into baroclinic energy, and the
H
_
F
_
term represents the portion
of the converted baroclinic energy that radiates from the conversion site. Local dissipation
occurs along with the conversion and radiation processes, and they are measured by the
barotopic (
0
+ D
0
) and baroclinic (
_
+ D
_
) dissipation terms, respectively. This
approach presents an exact measure of the barotropic-to-baroclinic tidal energy conversion.
3. Numerical simulations
We can implement the theoretical framework into a numerical ocean model and then use it
to analyze the tidal energy budget. In this section, we provide an example of the numerical
investigation of the tidal energetics in the Monterey Bay area along the central west coast of
the United States.
60 Energy Conservation
Barotropic and Baroclinic Tidal Energy 5
121 W
o
122
o
123
o
124
o
125
o
126
o
38 N
o
37
o
36
o
35
o
34
o
Elevation (m)
Moss
Landing
K
S
u
r
R
i
d
g
e
*
Sur
Platform
Davidson
Seamount
Figure 3. Bathymetry map of Monterey Bay and the surrounding open ocean. The black indicates a
eld observation station K. The domain outside the white box indicates the area affected by the sponge
layers in the simulations. The solid black line indicates the vertical transaction along which baroclinic
velocities are shown in Figure 5.
3.1. Model setup
Monterey Bay is featured by the prominent Monterey Submarine Canyon (MSC), numerous
ridges, smaller canyons, and a continental slope and break region. This area is exposed to the
large- and meso-scale variations of the California Current System as well as the tidal currents.
Energetic internal wave activity has been observed in MSC and the surrounding region. Due
to the complex bathymetry, tidal mixing processes in this area are of great interest. Our
simulation domain extends approximately 200 km north and south of Moss Landing, and 400
km offshore (Figure 3), which is large enough to allow the evolution of offshore-propagating
waves.
The ocean model we employ for this study is the SUNTANS model of Fringer et al. (2006).
The resolution of the horizontal unstructured grid smoothly transitions from roughly 80 m
within the Bay to 11 km along the offshore boundary. In the vertical, there are 120 z-levels
with thickness stretching from roughly 6.6 m at the surface to 124 m in the deepest location,
which provides better vertical resolution in the shallow regions. In total, the mesh consists of
approximately 6 million grid cells in 3D.
The initial free-surface and velocity eld are initialized as quiescent throughout the domain.
The initial stratication is specied with horizontally-homogeneous temperature and salinity
proles. At the coastline, we apply the no-ow condition, while at the three open boundaries
the barotropic velocities are specied with the OTIS global tidal model [2]. A sponge layer
is imposed at each of the open boundaries to absorb the internal waves and minimize the
61 Barotropic and Baroclinic Tidal Energy
6 Energy Conservation
reection of baroclinic energy into the domain. More model setup details and the validation
of the model skill can be found in Kang and Fringer (2012).
3.2. Tidal dynamics
Figure 4. Sea surface elevation at t = 18T
M
2
from M
2
forced barotropic run (left) and baroclinic run
(right). Bathymetry contours are spaced at -200, -500, -1000, -1500, -2000, -2500, -3000, -3500 m.
Monterey Bay is exposed to predominantly semidiurnal M
2
tide. Therefore we carry out two
sets of M
2
forced simulations, one with homogeneous density to investigate the barotropic
tides only, while the other with vertical stratication to study the baroclinic tides. Each
simulation is run for 18 M
2
tidal cycles. Sea-surface elevations from such two runs are
illustrated in Figure 4. This comparison highlights the modulation of baroclinic tides to the
barotropic ow eld, particularly near rough bottom topography.
Figure 5 demonstrates the vertical distribution of baroclinic velocities along a transect
indicated in Figure 3. It can be seen clearly that baroclinic tides are generated at Sur Platform
and then radiate to the north and south in the form of tidal beams.
4. Tidal energetics
We evaluate the depth-integrated, time-averaged barotropic and baroclinic energy equations
(11) and (12) for the energy analysis in this section. They are averaged over the last six M
2
tidal
cycles of the 18-M
2
-cycle baroclinic simulation. Because the system is periodic, the rst term
in equation (11)-(12) tends to zero upon period-averaging. We therefore obtain the balance
relations
F
0
_
=
C
_
0
+ D
0
, (13)
_
F
_
=
C
_
+ D
_
. (14)
The model computes all the energy terms in the barotropic and baroclinic equations. In the
following analysis, the conversion rate,
C
_
, and the energy ux divergence terms,
H
F
0
_
62 Energy Conservation
Barotropic and Baroclinic Tidal Energy 7
-15 -10 -5 0 5 10 15
(cm s )
-1
y - y (km) y - y (km)
K K
(a) (b)
Figure 5. Vertical structure of the East-West (a) and North-South (b) baroclinic velocities along the
transect indicated in Figure 3.
and
H
_
F
_
, are from direct model outputs. However, the barotropic and baroclinic
dissipation rates are inferred from the above balance relations as in Niwa and Hibiya (2004).
4.1. Horizontal structure
The left panel of Figure 6 illustrates the horizontal distribution of the depth-integrated
baroclinic energy ux vectors,
_
F
_
. Large energy uxes are seen in the vicinity of
rough topographical features, such as the MSC, the Sur Ridge-Platform region, and the
Davidson Seamount. The right panel of Figure 6 shows the horizontal distribution of
the depth-integrated barotropic-to-baroclinic conversion rate,
C
_
. Red color represents
positive energy conversion rate, which implies generation of internal tides, and negative
energy conversion rate (blue color) represents energy transfer from the baroclinic tide to the
barotropic tide. Negative energy conversion is due to the phase difference between locally-
63 Barotropic and Baroclinic Tidal Energy
8 Energy Conservation
0.2
0.1
0
-0.1
-0.2
1.3
1.2
0.9
0.6
0.3
0
(kW m ) (W m )
-1 -2
-3000m -200m -3000m -200m
Figure 6. Depth-integrated, period-averaged baroclinic energy ux,
_
F
_
(left), and
barotropic-to-baroclinic conversion rate,
C
_
(right). Darker bathymetry contours are 200 m and 3000 m
isobaths.
and remotely-generated baroclinic tides, and therefore indicates multiple generation sites
[23]. Signicant negative conversion occurs within the MSC because the locally generated
baroclinic tides interact with those generated at the North Sur Platform region. Large
baroclinic energy can be seen radiating from North Sur Platform into the MSC following
the canyon bathymetry from the gure. Figure 6 also shows that most of the generation
is contained within the 200-m and 3000-m isobaths. The baroclinic energy ux divergence,
_
F
_
, and the baroclinic dissipation rate,
H
_
F
C
_
, are shown in Figure 7s left
and right panels, respectively. Large baroclinic energy dissipation occurs near the locations of
strong internal tide generation.
4.2. Energy ux budget
The total power within a region is obtained by area-integrating the period-averaged and
depth-integrated energy terms to give
BT Input =
F
0
_
A, (15)
Conversion =
C
_
A, (16)
BC Radiation =
_
F
_
A, (17)
BT Dissipation =
F
0
_
+
C
__
A, (18)
BC Dissipation =
_
F
C
_
_
A, (19)
where implies summation of the grid cells within a particular region and A is the area of
each grid cell.
64 Energy Conservation
Barotropic and Baroclinic Tidal Energy 9
Figure 7. Depth-integrated, period-averaged baroclinic energy ux divergence,
H
_
F
_
(left), and
baroclinic dissipation rate,
H
_
F
C
_
(right).
As Figure 6 indicated, most of the baroclinic energy generation is within the 200-mand 3000-m
isobaths. We now depict the energy budget for the shelf and slope regions bounded by the
200-m and 3000-m isobaths Figure 8. Barotropic energy is lost at a rate of 147 MW to the
slope region and approximately 87% of this energy is converted into baroclinic energy. Most
of this generated baroclinic energy is dissipated locally, while the remaining portion (38%) is
radiated. The shelf region acts as a baroclinic energy sink because it dissipates both the energy
generated locally and the portion owing into it from the slope region.
Two efciency parameters are dened to examine the characteristics of baroclinic energy
conversion and radiation, respectively,
c
=
Conversion
BT Input
, (20)
r
=
BC Radiation
Conversion
. (21)
Figure 9 compares the conversion and radiation efciency for ve subdomains (a)-(e).
Subdomain (a), a 200 km 230 km domain, is used to represent the Monterey Bay area
because it includes all typical topographic features in this area. This comparison demonstrates
that the tidal energy conversion and radiation depend strongly on topographic features. The
Davidson Seamount and the Northern shelf-break region are the most efcient topographic
features to convert ( 94%) barotropic energy into baroclinic energy and then let it radiate
out into the open ocean (> 75%). The Sur Platform region also converts a large portion (88%)
and radiates more than half of the barotropic energy as baroclinic energy. The MSC acts as an
energy sink because it does not radiate energy but instead absorbs the baroclinic energy from
the Sur Platform region.
65 Barotropic and Baroclinic Tidal Energy
10 Energy Conservation
1.3
1.2
0.9
0.6
0.3
0
(kW m )
-1
-3000m -200m
Figure 8. Schematic of the M
2
tidal energy budget for the two subdomains bounded by the 0-m, 200-m
and 3000-m isobaths.
1.3
1.2
0.9
0.6
0.3
0
(kW m )
-1
(b) North Shelf Break
(c) MSC
(d) Sur Region
(e) Davidson
Seamount
(a)
Region
1
=
s
, (22)
where is the topographic slope, and s is the internal wave characteristic slope. The steepness
parameter is used to distinguish between subcritical (
1
< 1) and supercritical topography
(
1
> 1). The topography is referred to as critical when
1
= 1.
67 Barotropic and Baroclinic Tidal Energy
12 Energy Conservation
The second nondimensional parameter is the tidal excursion parameter dened by
2
=
U
0
k
b
, (23)
which measures the ratio of the tidal excursion U
0
/ to the horizontal scale of the topography
k
1
b
.The excursion parameter is used to examine the nonlinearity of the waves [6, 15, 20].
When
2
1, linear internal tides are generated mainly at the forcing frequency . Over
subcritical topography (
1
< 1) most of the energy generation is in the rst mode internal tide,
while over critical or supercritical topography (
1
1), higher modes are generated and their
superposition creates internal tidal beams. At intermediate excursion (
2
1), nonlinearity
becomes important, and nonlinear internal wave bores, weak unsteady lee waves, and solitary
internal waves may be generated depending on the topographic features. When
2
> 1, in
addition to bores and solitary internal waves, strong unsteady lee waves may form [22].
Although internal wave generation is a complex process, we can summarize the behavior of
the internal wave generation in Monterey Bay by plotting histograms of the conversion and
divergence terms as functions of the criticality and excursion parameters. Here we compute
the two parameters throughout subdomain (a). The upper and left panels of Figures 11
demonstrate the distribution of conversion as a function of the nondimensional parameters
1
and
2
, respectively. The energy conversion (green bins) occurs predominantly in regions
within which
1
< 5 and
2
< 0.02. Under these conditions, baroclinic tides generated in this
region are mainly linear and in the form of internal tidal beams [6, 20, 22]. As expected,
conversion of barotropic energy into baroclinic energy peaks for critical topography near
1
1. More interesting, however, is that there is also a peak in conversion for a particular
value of
2
0.005.
The lower right panel of Figure 11 depicts the distribution of the energy conversion as a
function of the two parameters. Energy conversion occurs mainly in regions where
1
and
2
satisfy a particular relation. When both parameters are small, this relation is linear. As the
values of the two parameters increase, the departure is weakly quadratic.
6. Summary
The tides are one of the main power to mix the ocean, which is the largest energy collector from
the Earth-Moon system. A better understanding of how and where the tides lost their energy
is very important to the climate and energy study. In this chapter, we present a numerical
method to investigate the tidal energy conversion and estimate the tidal energy budget.
A theoretical framework for analyzing tidal energetics is derived based on the complete
form of the barotropic and baroclinic energy equations that provide an accurate and detailed
energy analysis. Three-dimensional, high-resolution simulations of the tides and waves in the
Monterey Bay area are conducted using the hydrodynamic coastal SUNTANS ocean model.
Based on the theoretical approach, model results are analyzed to address the question of
how the barotropic tidal energy is partitioned between local barotropic dissipation and local
generation of baroclinic energy, and then how much of this generated baroclinic energy is
lost locally versus how much is radiated away for open-ocean mixing. Subdomain (a), a
200 km 230 km domain, is used to represent the Monterey Bay area because it includes
68 Energy Conservation
Barotropic and Baroclinic Tidal Energy 13
sLeepness
e
x
c
u
r
s
l
o
n
4
3
2
1
0
(MW)
0.013
0.01
0.003
0
Figure 11. Distribution of the barotropic-to-baroclinic energy conversion as a function of steepness
parameter
1
and excursion parameter
2
for subdomain (a).
all typical topographic features in this region. Of the 152 MW energy lost from the barotropic
tide, approximately 133 MW (88%) is converted into baroclinic energy through internal tide
generation, and 42% (56 MW) of this baroclinic energy radiates away for open-ocean mixing
(Figure 12). The tidal energy partitioning depends greatly on the topographic features. The
Davidson Seamount and the Northern shelf-break region are most efcient at baroclinic
energy generation and radiation. The Sur Platform region converts a large portion and
radiates roughly half of the barotropic energy as baroclinic energy. The Monterey Submarine
Canyon acts as an energy sink because it does not radiate energy but instead absorbs the
baroclinic energy from the Sur Platform region. The energy ux contributions from nonlinear
and nonhydrostatic effects are also examined. The small advection and nonhydrostatic
contributions imply that the internal tides in the Monterey Bay area are predominantly linear
and hydrostatic.
We also investigate the character of tidal energy conversion by examining the energy
distribution as a function of two nondimensional parameters, namely the steepness parameter
(
1
= /s) and the excursion parameter (
2
= U
0
k
b
/). The generation mainly occurs in the
regions satisfying
1
< 5 and
2
< 0.02, indicating that baroclinic tides generated in the
Monterey Bay area are mainly linear and in the form of internal tidal beams. The results
highlight how description of the conversion process with simple nondimensional parameters
produces results that are consistent with theory, in that internal wave energy generation
peaks at critical topography (
1
1). The results also indicate that conversion peaks for
a particular excursion parameter (
2
0.005 for this case). This implies that it may be
possible to parameterize conversion of barotropic to baroclinic energy in barotropic models
69 Barotropic and Baroclinic Tidal Energy
14 Energy Conservation
Topography
Baroclinic Tides
Barotropic Tides
Internal Waves
Local Mixing Deep Ocean Mixing
100%
88% (100%)
37% (42%)
12%
(58%) 51%
Figure 12. Schematic of the M
2
tidal energy budget in percentages for subdomain (a) indicated in Figure
9. The bold percentages are relative to the total input barotropic energy, and the thin italic percentages
are relative to the generated baroclinic energy.
with knowledge of
1
and
2
. For example, a parameterization of internal wave generation
based on the steepness parameter has been widely used in global barotropic tidal models [21]
and ocean general circulation models [10].
This work outlines a systematic approach to analyze internal tide energetics and estimate tidal
energy budget regionally and globally. The results draw a picture of how the M
2
tidal energy
is distributed in the Monterey Bay region. The Monterey Bay area is exposed to the large-scale
California Current System and meso-scale eddies and upwelling. The seasonally varying
dynamics may affect the stratication and thus the generation and propagation of internal
tides in this area. Therefore, it may be necessary to consider seasonal effects of stratication
and to include mesoscale effects by coupling with a larger-scale regional model such as ROMS
[8, 19].
Acknowledgements
The author gratefully acknowledge the support of Professor Oliver Fringer at Stanford
University and the ONR Grant. I would like to thank Samantha Terker, Drs. Jody Klymak,
Robert Pinkel, James Girton, and Eric Kunze for kindly providing the eld data. The helpful
discussions with Drs. Robert Street, Stephen Monismith, Leif Thomas, and Rocky Geyer are
greatly appreciated. I also thank Dr. Steven Jachec for useful help with simulation setup.
Author details
Dujuan Kang
Institute of Marine and Coastal Sciences, Rutgers University, New Jersey, USA
70 Energy Conservation
Barotropic and Baroclinic Tidal Energy 15
7. References
[1] Carter G.S (2010) Barotropic and baroclinic M2 tides in the Monterey Bay region. J. Phys.
Oceanogr. 40: 1766-1783.
[2] Egbert G.D, Erofeeva S.Y (2002) Efcient inverse modeling of barotropic ocean tides. J.
Atmos. Oceanic Technol. 19: 183-204.
[3] Egbert G.D, Ray R.D (2000) Signicant dissipation of tidal energy in the deep ocean
inferred from satellite altimeter data. Nature. 405: 775-778.
[4] Egbert G.D, Ray R.D (2001) Estimates of M2 tidal energy dissipation from
TOPEX/Poseidon altimeter data. J. Geophys. Res. 106(C10): 22475-22502.
[5] Fringer O.B, Gerritsen M, Street R.L (2006) An unstructured-grid, nite-volume,
nonhydrostatic, parallel coastal ocean simulator. Ocean Modelling. 14: 139-173.
[6] Garrett C, Kunze E (2007) Internal tide generation in the deep ocean. Annu. Rev. Fluid
Mech. 39: 57-87.
[7] Gill A.E (1982) Atmosphere-Ocean Dynamics. Academic Press.
[8] Haidvogel D.B, Arango H.G, Hedstrom K, Beckmann A, Malanotte-Rizzoli P,
Shchepetkin A.F, 2000: Model evaluation experiments in the North Atlantic Basin:
Simulations in nonlinear terrain-following coordinates. Dyn. Atmos. Oceans. 32:
239-281.
[9] Jachec S.M, Fringer O.B, Gerritsen M.G, Street R.L (2006) Numerical simulation of
internal tides and the resulting energetics within Monterey Bay and the surrounding
area. Geophys. Res. Lett. 33: L12605, doi:10.1029/2006GL026314.
[10] Jayne S.R (2009) The impact of abyssal mixing parameterizations in an ocean general
circulation model. J. Phys. Oceanogr. 39: 1756-1775.
[11] Kang D. (2010) Energetics and dynamics of internal tides in Monterey Bay using
numerical simulations. Ph.D. Dissertation. Stanford University. 170 p.
[12] Kang D, Fringer O.B (2010) On the calculation of available potential energy in internal
wave elds. J. Phys. Oceanogr. 40: 2539-2545.
[13] Kang D, Fringer O.B (2012) Energetics of barotropic and baroclinic tides in the Monterey
Bay area. J. Phys. Oceanogr. 42: 272-290.
[14] Lamb K.G (2007) Energy and pseudoenergy ux in the internal wave eld generated by
tidal ow over topography. Cont. Shelf Res. 27: 1208-1232.
[15] Legg S, Huijts K.M.H (2006) Preliminary simulations of internal waves and mixing
generated by nite amplitude tidal ow over isolated topography. Deep-Sea Res. II. 53:
140-156.
[16] Munk W, Wunsch C (1998) Abyssal recipes II: Energetics of tidal and wind mixing.
Deep-Sea Res. 45: 1977-2010.
[17] Niwa Y, Hibiya T (2004) Three-dimensional numerical simulation of M2 internal tides
in the East China Sea. J. Geophys. Res. 109: C04027, doi:10.1029/2003JC001923.
[18] Polzin K.L, Toole J.M, Ledwell J.R, Schmitt R.W (1997) Spatial variability of turbulent
mixing in the abyssal ocean. Science. 276: 93-96.
[19] Shchepetkin A.F, McWilliams J.C (2005) The Regional Oceanic Modeling System:
A split-explicit, free-surface, topography-following-coordinate ocean model. Ocean
Modelling. 9: 347-404.
[20] St. Laurent L, Garrett C (2002) The role of internal tides in mixing the deep ocean. J.
Phys. Oceanogr. 32: 2882-2899.
71 Barotropic and Baroclinic Tidal Energy
16 Energy Conservation
[21] St. Laurent L, Simmons H.L, Jayne S.R (2002) Estimating tidally driven mixing in the
deep ocean. Geophys. Res. Lett. 29: 2106-2110.
[22] Vlasenko V, Stashchuk N, Hutter K (2005) Baroclinic Tides: Theoretical Modeling and
Observational Evidence. Cambridge University Press.
[23] Zilberman N.V, Becker J.M, Merrield M.A, Carter G.S (2009) Model estimates of M2
internal tide generation over Mid-Atlantic Ridge topography. J. Phys. Oceanogr. 39:
2635-2651.
72 Energy Conservation
Chapter 3
Understanding Energy Conservation:
Intersection Between Biological
and Everyday Life Contexts
Vivien Mweene Chabalengula and Frackson Mumba
Additional information is available at the end of the chapter
http://dx.doi.org/10.5772/51872
1. Introduction
Energy and energy conservation (which is also the First Law of Thermodynamics) are such
closely related concepts that it is almost impossible to discuss one without the other in a
closed system (Goldring & Osborne, 1994). Energy is commonly defined as the capacity to do
work (Lee & Liu, 2010), such as driving metabolic reactions and processes (e.g.
photosynthesis, muscle contraction) in biological systems. On the other hand, the energy
conservation principle is commonly stated as energy cannot be created or destroyed (Raven &
Johnson, 1999) in almost all science textbooks. However, many science educators argue that
this definition may be confusing among students if supporting concepts such as energy
transfer, energy flow, and energy transformation (Mclldowie, 1995; Chabalengula et al,
2012) are not incorporated when defining energy conservation. This is because all energy
forms are inter-convertible from one form to another without any loss; and any apparent loss
of energy can be explained as the conversion/transformation of energy into some other form
(Raven & Johnson, 1999; Solomon et al, 1993).
The concepts of energy and energy conservation are central scientific ideas which provide
an important key to our understanding of the way things happen in the biological, physical,
and technological world (Liu, Ebenezer & Fraser, 2002). Furthermore, energy is one of the
science concepts that cuts across all science disciplines, and is experienced in our everyday
life situations (Saglam-Arslan & Kurnaz, 2009).
However, the synonymous use of the terms conservation and saving in everyday language
usage causes students to misunderstand the scientific meaning of the energy conservation
principle. With the current national and global debates on energy saving reality coming to
agenda with energy crisis, many students think of energy conservation as energy saving
Energy Conservation
74
because the latter term is used when issues on depleting energy sources are discussed in
media and political realms (Tatar & Oktay, 2007). As such, it is imperative that school-going
citizens are scientifically literate about what energy conservation is if they are to delineate
energy conservation and energy saving. Therefore we propose that it is vital for science
educators to determine students understanding of energy conservation from a scientific
(particularly biological context) and an everyday life context. These two contexts are
particularly important because they are interrelated in that biological contexts such as
jogging and breathing are always experienced by students on each daily basis so much that
they can relate to them very well. Therefore, a compilation of students understanding of
energy conservation based on these two contexts would provide a set of energy
conservation data that can be used as a basis for science education curriculum development
and instructional design in schools (Lee, 2011).
1.1. Energy conservation principle
According to the energy conservation principle (also known as the first law of
thermodynamics), energy cannot be created or destroyed; instead it can be converted from
one form to another (Raven & Johnson, 1999; Solomon et al, 1993). All energy forms are
inter-convertible from one form to another without any loss. Any apparent loss of energy
can be explained as the conversion of energy into some other form. For example, in
biological/living systems, some of the energy is used to drive metabolic processes and some
of it dissipates to the atmosphere in the form of heat. Therefore, energy as a conserved
quantity at the system level is built upon many supporting concepts such as energy source,
energy transfer, energy flow, and energy transformation (Mclldowie, 1995).
The description of energy flow and transformations is frequently used in many biological
and technological applications (Ametller & Pinto, 2002; Lin & Hu, 2003). For instance, in
biological systems, energy flows from sources such as the sun and moves through a number
of carriers to eventual receivers, such as through producers (mostly plants which utilize
energy to produce food during photosynthesis) to consumers (animals) in food chains. That
is, plant cells transform light energy to chemical energy stored in chemical bonds of food
materials. When some herbivores eat the plants, some of this chemical energy is eventually
converted to mechanical energy in animals for muscle contraction (useful work), whereas
some of it may dissipate to the atmosphere in form of heat energy (Raven & Johnson, 1999).
As all these metabolic processes are happening, there is no loss; instead any seemingly loss
is explained in terms of energy conversion/transformation. Given the scientific viewpoint of
energy conservation especially in biological systems, it is important to remind readers that
this concept poses conceptual difficulties among students, as highlighted in the next section.
1.2. Problematic concerns about energy conservation in biology education
As stated earlier on, the energy conservation principle is commonly stated as energy cannot
be created or destroyed in most science textbooks. Due to its common appearance in
textbooks and its short definition, Tatar and Oktay (2007) point out that energy conservation
Understanding Energy Conservation: Intersection Between Biological and Everyday Life Contexts
75
is one of the most known science principles among students as it is easy to state and
remember. As such when asked to state the energy conservation principle, many students
tend to recite it with relative easiness, but they are unable to correctly apply it to biological
systems. Therefore, the two problematic aspects that make energy conservation a difficult
concept to understand among students are:
a. Despite being able to recite it correctly, many students are unable to apply this
principle, particularly to biological systems and processes as well as in everyday life
situations involving energy (Chabalengula et al, 2012). Part of the reason for this
problem has been highlighted by Driver and Warrington (1985, p. 171) who asserted
that very rarely do students consider energy as a conserved quantity; rather it is
something that is active for a short period and then disappears.
b. The synonymous use of the terms conservation and saving in daily life causes students to
misunderstand the energy conservation principle (as discussed earlier on).
The two problems stated above led to our motivation to look at the science education
literature and determine the extent to which the science education research has tried to
remediate the problems. Two issues became evident: First, a review of the previous
instruments aimed at diagnosing students understanding of energy conservation shows
that the focus was mainly in physics and engineering contexts rather than in biological
contexts. Second, very few studies have used test items which reflected the everyday life
situations despite the findings that students have ideas about energy conservation from this
perspective. In our opinion, the students conceptual difficulties with respect to energy
conservation are interrelated and connected to other aspects such as everyday life and
science discipline contexts, which have not been sufficiently taken into account in previous
diagnostic research.
Therefore in this book chapter, we will present findings from the diagnosis we conducted
with 90 university biology students understanding of energy conservation using the pencil
and paper test, reflecting test items phrased in the biological and everyday life situations,
we developed specifically for this study.
1.3. Previous studies on students understanding of energy conservation
The science education research has shown that students of all ages have conceptual
difficulties and misunderstandings related to the meaning of energy conservation (e.g.
Goldring & Osborne, 1994; Pinto et al, 2005), and the application of energy conservation in
biological systems (e.g. Barak et al, 1997; Eisten & Stavy, 1988; Fetherston, 1999; Gayford,
1986; Goldring & Osborne, 1994; Kesidou et al, 1993; Kruger et al, 1992; Linjse, 1990; Mann,
2003; Solomon, 1982; Trumper, 1997).
Table 1 shows some previous studies (in chronological order) and the corresponding
student errors about energy conservation meanings and applications in biological systems.
With respect to what energy conservation means, several researchers have found two
common errors: energy conservation means energy saving; and energy conservation is
Energy Conservation
76
Some erroneous ideas
about energy
conservation, as
identified by different
researchers
S
o
l
o
m
o
n
(
1
9
8
2
)
n
=
o
n
e
c
l
a
s
s
(
E
n
g
l
i
s
h
c
o
m
p
r
e
h
e
n
s
i
v
e
s
c
h
o
o
l
)
G
a
y
f
o
r
d
(
1
9
8
6
)
n
=
2
9
6
(
E
n
g
l
i
s
h
A
-
l
e
v
e
l
b
i
o
l
o
g
y
E
i
s
t
e
n
e
t
a
l
(
1
9
8
8
)
n
=
1
8
8
(
I
s
r
e
a
l
i
h
i
g
h
s
c
h
o
o
l
&
u
n
i
v
e
r
s
i
t
y
L
i
n
j
s
e
(
1
9
9
0
)
n
=
9
7
(
D
t
h
h
i
h
h
l
t
d
t
)
K
r
u
g
e
r
e
t
a
l
(
1
9
9
2
)
n
=
1
5
9
(
E
n
g
l
i
s
h
p
r
i
m
a
r
y
s
c
h
o
o
l
t
e
a
c
h
e
r
s
)
K
e
s
i
d
o
u
e
t
a
l
(
1
9
9
3
)
n
=
3
4
(
G
e
r
m
a
n
h
i
g
h
s
c
h
o
o
l
s
t
u
d
e
n
t
s
)
G
o
l
d
r
i
n
g
e
t
a
l
(
1
9
9
4
)
n
=
7
5
(
E
n
g
l
i
s
h
h
i
g
h
s
c
h
o
o
l
s
t
u
d
e
n
t
s
)
B
a
r
a
k
e
t
a
l
(
1
9
9
7
)
n
=
1
0
4
(
7
6
&
2
8
I
s
r
a
e
l
i
h
i
g
h
s
c
h
o
o
l
T
r
u
m
p
e
r
(
1
9
9
7
)
n
=
1
8
9
(
I
s
r
a
e
l
i
p
r
e
-
s
e
r
v
i
c
e
b
i
o
l
o
g
y
F
e
t
h
e
r
s
t
o
n
(
1
9
9
9
)
n
=
9
4
(
A
u
s
t
r
a
l
i
a
n
h
i
g
h
s
c
h
o
o
l
s
t
u
d
e
n
t
s
)
M
a
n
n
(
2
0
0
3
)
n
=
6
1
0
(
A
u
s
t
r
a
l
i
a
n
h
i
g
h
s
c
h
o
o
l
s
t
u
d
e
n
t
s
)
P
i
n
t
o
e
t
a
l
(
2
0
0
5
)
n
=
2
0
(
S
p
a
n
i
s
h
h
i
g
h
s
c
h
o
o
l
s
c
i
e
n
c
e
Errors relating to meaning of energy conservation
Energy conservation is
synonymous to energy
saving
30%
Energy conservation is
the opposite of energy
degradation
Errors relating to application of energy conservation in biological systems
Students responses to
energy-related concepts
do not reflect (or if they
do, contradict) the idea
of energy conservation
in biological systems
79%
100
%
31%
Energy is created or
formed during
respiration
7%
Energy is used up or
consumed during
processes in living
things
29% 15%
Energy loss & decrease
during physical
activities (e.g. exercises)
in living systems are
erroneously interpreted
as a decrease in its
quantity
Table 1. Summary of students erroneous ideas about energy conservation
Note: *represents that a corresponding error was observed, but no exact percentages of students
holding the error was given.
Understanding Energy Conservation: Intersection Between Biological and Everyday Life Contexts
77
opposite of energy degradation. With respect to the application of energy conservation,
many researchers have found a conceptual failure among students to apply the energy
conservation principle (energy cannot be created or destroyed) to biological situations
involving energy. That is, the most common errors identified are: energy is created or
formed during respiration; energy is used up or consumed during metabolic processes; and
energy is lost during physical activities in living organisms. Energy loss and decrease in
energy phases are erroneously interpreted as a decrease in its quantity, and not a decrease in
energys usefulness (a correct scientific viewpoint). Scientifically, all energy forms are inter-
convertible from one form to another without any loss of energy. Similarly, in all biological
processes there is the same amount of energy before as after an event (Starr &Taggart, 1992).
However, as shown in Table 1, previous research shows that many students do not realise
that energy is conserved in biological processes and systems. Kesidou et al (1993) explain
that students often reject the idea of energy conservation because it seems to contradict
everyday experiences and language usage where energy is often viewed as being produced
and consumed, but not conserved. As such it is important to point out here that some
students who seem to have erroneous ideas about energy conservation may be influenced
by a language problem, and not a conceptual one. It is possible that whilst students use
terms such as used up and lost, some of them may use these terms figuratively, and not
actually conceptualize energy as not being conserved.
1.4. Aims of the chapter
Based on the concerns outlined above, and the previous studies done on students
understanding of energy conservation, the aims of this chapter are three fold: (a) To present
the data and results we found on students understanding of energy conservation in
biological and everyday contexts; (b) To develop a diagnostic instrument which can be used
to diagnose students understanding of energy conservation; and (c) To provide suggestions
on how biology educators can design their science curriculum and instruction in order to
help students understand and apply the concept of energy conservation to biological
systems.
The three research questions that guided this study were: (1) Are students able to state the
energy conservation principle? (2) To what extent are students able to apply the energy
conservation principle to everyday life situations involving biological phenomena? (3) Do
students understand what happens to energy during metabolic processes in
biological/living organisms?
2. Data collection methods and analysis
2.1. Sample description
The sample consisted of 90 first-year biology students at a South African university. There
were 40 males and 50 females. All these students were in a pre-medical program in which
they were preparing to go to medical school.
Energy Conservation
78
2.2. Development of energy conservation diagnostic test
A survey approach was used for this research, using a pencil-and-paper diagnostic test
specifically developed to collect the data. The design of the diagnostic test was based on a
process described by Haslam and Treagust (1987). The development of the test involved two
main phases: the preparatory and the test formulation phases. The preparatory phase
involved three steps. Step 1 involved the drawing up a list of scientifically acceptable
propositional knowledge statements about energy conservation and in biological-context.
This list was drawn up after interviewing three biology lecturers and then consulting the
two prescribed tertiary level textbooks for first-year biology courses at the university where
the study was conducted (i.e. Raven & Johnson, 1999; Solomon et al., 1993). The purpose of
this step was to draw up the energy conservation conceptual structure that defined this
study, and which was used as a guide when constructing the test items, and when marking
the answers. The energy conservation conceptual structure we came up with is summarized
below:
According to the first law of thermodynamics (the law of conservation of energy),
energy cannot be created or destroyed, but it can be converted from one form to another
work.
All energy forms are inter-convertible from one form to another without any loss.
Any apparent loss of energy can be explained as the conversion of energy into some
other form. For example, during each energy conversion in living systems, some of the
energy is used to drive the metabolic processes and some of it dissipates to the
atmosphere in the form of heat.
In biological systems, most reactions of organisms involve a complex series of energy
transformations. For example, during photosynthesis, plant cells transform light energy
to chemical energy stored in chemical bonds of food materials. Some of this chemical
energy may eventually be converted to mechanical energy in animals for muscle
contraction, if the plant is eaten by an animal.
Step 2 involved compiling a list of common erroneous ideas about energy conservation,
reported in the research literature (see Table 1). The purpose of this step was to compile a
list of ideas about energy conservation held by students in previous research studies, so
these could be included in the diagnostic test to be developed. Step 3 involved defining the
content boundaries of the test so that topics which students were expected to know when
they enter first year would be included in the test, in order for the test to be used to diagnose
prior knowledge as well. The information for this step was acquired through interviews
with lecturers who provided data on the prerequisite knowledge required in first year
biology.
In the test formulation phase, the diagnostic test had to fulfill two basic criteria: checks basic
knowledge about energy conservation; and tests understanding of energy conservation.
Testing for understanding is not an easy matter. Various authors have listed criteria that
could be used in judging understanding. For example, Sanders and Mokuku (1994) stated
that individuals who understand a concept should: know and be able to recognize the name
Understanding Energy Conservation: Intersection Between Biological and Everyday Life Contexts
79
and definition of a concept; be able to define and explain the concept in their own words; be
able to recognize instances not previously encountered of the concept; be able to distinguish
between and classify instances and non-instances of the concept not previously encountered;
and be able to apply the concept to new situations. Through these criteria, it is possible for
science educators to determine for sure, their students understanding level. A number of
these criteria were considered when designing the test. For example, the test items were
constructed in such a way that students were required to state energy conservation in their
own words, and to apply their understanding of energy conservation in the closed
statements reflecting biological and everyday life scenarios.
2.3. Energy conservation diagnostic test
The test consisted of three questions. Question 1 was an open-ended and aimed at eliciting
students understanding of the energy conservation principle. Actual Question 1 read: What
does the energy conservation principle state? Question 2 consisted of closed-ended statements
phrased in everyday life contexts but reflecting biological phenomena (see Table 3 for the
actual statements). These statements were meant to determine the extent to which students
are able to apply their understanding of energy conservation in the biological and everyday
life situations. The actual Question 2 read: Below are some statements about energy reflecting
everyday life situations and biological phenomena. Task 1 (a) For each statement, indicate by placing
a tick () in the appropriate box if the statement is scientifically correct or incorrect; (b)Then indicate
how sure you are that the answer you have provided is correct by ticking the appropriate box on
Sure, Think so or Guessing. Task 2 (a) If the statement is incorrect, underline the word or
phrase in the statement which makes it incorrect; and (b) Then write in a word or phrase which would
make the statement correct. Question 3 was open-ended and was meant to elicit students
conceptual understanding of what happens to energy during metabolic processes in living
organisms. The actual question 3 read: Energy is required to drive metabolic processes (such as
breathing, muscle contraction) in living organisms. Explain what you think happens to energy
during metabolic processes.
Quality-control steps taken while the instrument was developed included checks on
content validity, and rigorous face validation by three university biology experts. The
instrument was piloted with 30 first-year biology students who were not involved in the
main study. Piloting is an important quality-control procedure as it enables to check on
the suitability of individual test items; to gain feedback on how well participants
understood the questions, response procedures and instructions so that questions can be
improved (Bell, 1987). The pilot group was requested to indicate whether they had
problems understanding what they were required to do in each question and each closed
statement. They were also further requested to write down the words or phrases which
were not clear to them. The results of the pilot showed that majority of the students who
indicated having problems suggested their inability to give answers due to lack of
knowledge about energy conservation, and not based on misunderstanding the items. As
such all test items were maintained.
Energy Conservation
80
3. Data analysis
The data were analysed using open-coding and reported as frequency counts and
percentages. After a line-by-line analysis of each script, categories and sub-categories to
which responses would fit well were developed. The categories which had been developed
were given to two biology experts for validation. These experts were asked to check for the
following: the scientific correctness of the answers given by students, the appropriateness of
the categories developed for the student answers, and whether the students responses were
correctly categorised. This was done by giving each expert ten scripts to go through and
code independently. Any differences in the coding were discussed collectively, and a
common agreement reached. When individuals rate a product, there is always a possibility
that some portion of the agreement between them is due to chance. As such, Cohen (1960)
recommends using the kappa statistic to assess interrater agreements involving nominal
scale. Cohens Kappa (k) is a coefficient of interrater agreement that takes into consideration
agreement by chance. The interrater agreements between the biology educators on the
scientific correctness of the answers provided by students are shown in Table 2.
Test item Percent agreement Kappa value
Definitions of energy conservation principle.
Explanations of what happens to energy during
metabolic processes.
96
87
0.90
0.85
Table 2. Interrater agreement values
The percentage of agreement ranged from 87 % to 96% with a corresponding kappa
coefficients range of 0.85 to 0.90. The percentage agreement of more than 75% and kappa
values above 0.5 are considered to indicate good level of interrater agreement (Chiapetta,
Fillman & Sethna, 1991). Therefore, the values in this study can be considered good enough
to justify reliability. After the categorization process on the scientific correctness of the
responses, frequency counts were conducted to get the actual number of students giving
each answer, and to calculate the percentages.
4. Results and discussion
The results have been presented along with the discussion. This is because certain aspects of
energy such as what happens to energy during metabolic processes need to be discussed
alongside the scientifically acceptable perceptions so that the reader(s) can have a clearer
perspective as to why the authors of the current study categorized some statements as
scientifically correct or incorrect.
4.1. Stating the energy conservation principle
Nearly all students (98%) correctly stated the principle of energy conservation (i.e. energy
cannot be created or destroyed). This finding is supported by Tatar et al (2007) who pointed
Understanding Energy Conservation: Intersection Between Biological and Everyday Life Contexts
81
out that this principle is widely known among students due to its easiness in stating and
remembering so much that when asked to state it, students do recite it correctly.
However, majority of the students in this study still reverted back to their everyday
understanding of energy being used up, created or lost during activity, when they had to
apply this principle in closed-ended biological and everyday context statements. This
implies that even though these students can correctly state the energy conservation
principle, they do not understand it fully so as to apply it to biological situations.
4.2. Application of energy conservation principle in biological situations
Students understanding and application of energy conservation were elicited using the
closed statements that involved biological phenomena presented in everyday life situations,
as shown in Tables 3 and 4. Table 3 shows students responses on the correctness of each
statement, and their confidence level of their answers. Table 4 shows students responses on
word/phrase they believed made a statement incorrect, as well as the word/phrase they
would write-in to make a statement correct. However, one important point to note as one
reads the results in this section is that many students (38%) did not attempt to underline the
word or phrase making the statement(s) incorrect, or to write in the word or phrase which
would correct the statement(s) which they had indicated were incorrect. The possible
validity problem associated with this is that it is not clear whether the students who did not
give responses did not follow the instructions, or whether this indicated a lack of
understanding of the energy conservation principle. As such, it would have been of value to
interview some of these students. However, interviews were not conducted because one of
the purposes for this study was to develop a pencil-and-paper diagnostic test that could be
used to diagnose students understanding of energy conservation, and which biology
educators can easily administer. The specific findings pertaining to students ability to apply
the energy conservation principle are provided in the next subsections.
Test Statements
How sure are you statement is
correct
How sure are you statement is
incorrect
S
t
a
t
e
m
e
n
t
C
o
r
r
e
c
t
S
u
r
e
T
h
i
n
k
s
o
G
u
e
s
s
i
n
g
S
t
a
t
e
m
e
n
t
I
n
c
o
r
r
e
c
t
S
u
r
e
T
h
i
n
k
s
o
G
u
e
s
s
i
n
g
If you go jogging,
energy is used up*.
83 (92%) 73 (88%) 10 (12%) 0 6 (7%) 5 (83%) 1 (17%) 0
After exercise, you
can build up your
energy levels by
resting*.
39 (43%) 18 (46%) 17 (44%) 4 (10%) 50 (56%) 17 (34%) 32 (64%) 0
Energy Conservation
82
When you are
asleep your body
does not require
any energy because
it is not active*.
6 (7%) 4 (67%) 2 (33%) 0 83 (92%) 71 (86%) 9 (11%) 0
During exercise,
energy is built up
in the body*.
14 (16%) 6 (43%) 7 (50%) 0 74 (82%) 47 (64%) 23 (31%) 3 (4%)
When living things
are active, they lose
energy*.
53 (59%) 30 (57%) 18 (34%) 3 (6%) 36 (40%) 20 (56%) 15 (42%) 0
Table 3. Students responses on correctness of statements, and how sure they were about their answers.
Notes: Figures outside the brackets represent the actual number of students who responded.
* Statement is scientifically incorrect.
Number of students who did not attempt the test item 34 (38%)
Number of students who responded to the test item 56 (62%)
Statements
reflecting biological
phenomena
Task 1 Task 2
Underlined
word or
phrase which
makes
statement
incorrect
A
c
t
u
a
l
n
u
m
b
e
r
o
f
s
t
u
d
e
n
t
s
%
o
f
w
h
o
r
e
s
p
o
n
d
e
d
%
o
f
w
h
o
l
e
a
l
e
Written-in
Word or phrase
which makes
statement
correct
N
u
m
b
e
r
o
f
s
t
u
d
e
n
t
s
%
o
f
w
h
o
r
e
s
p
o
n
d
e
d
%
o
f
w
h
o
l
e
s
a
m
p
l
e
If you go jogging,
energy is used up*
Incorrect
phrase
-used up
4
7
4
Acceptable
- converted to
different forms
Unacceptable
-lost
3
1
5
2
3
1
After exercise, you
can build up your
energy levels by
resting*
Incorrect
phrase
-build up
9
16
10
Acceptable
-do not build
up
4
7
4
Incorrect word
-resting
22
39
25
Acceptable
-eating(food
consumption)
Unacceptable
-stop using
energy
15
3
27
6
16
4
Understanding Energy Conservation: Intersection Between Biological and Everyday Life Contexts
83
When you are asleep
your body does not
require any energy
because it is not
active*
Incorrect
phrase
-does not
require energy
because it is
not active
47
84
52
Acceptable
-require energy
as it is still
active
- many body
processes (e.g.
respiration) still
occur
21
8
37
14
23
9
During exercise,
energy is built up in
the body*
Incorrect
phrase
-built up
42
75
47
Acceptable
- converted to
different forms
Unacceptable
- used up
- lost
7
23
7
12
41
13
8
26
8
When living things
are active, they lose
energy*
Incorrect word
-lose
25
45
28
Acceptable
-convert it to
different forms
Unacceptable
-use up
7
10
12
18
7
11
Table 4. Students responses on words/phrases making the statements incorrect, and how they would
correct them.
Note: * Statement is scientifically incorrect
4.2.1. Ideas relating to energy being used up when an organism is active
The idea that energy is used up during activities was erroneously accepted by majority of the
students. That is, 92% of them erroneously indicated that the statement If you go jogging,
energy is used up, is correct and most of these students (73 of them) were sure their response
was correct. To the contrary, only 6 students correctly indicated that the statement is
incorrect. When asked to underline the phrase making the statement incorrect, only four of
the six students (who indicated that the statement was incorrect) correctly underlined the
phrase used up. Three of these students correctly wrote in the phrase energy is converted
into different forms. One student wrote in the word lost, however without the added
explanation that heat energy is lost to the body during respiration, this answer has to be
judged as erroneous.
The idea that energy is used up during activities and in processes is documented by many
researchers (e.g. Linjse, 1990; Kesidou & Duit, 1993; Fetherston, 1999). For example, Kesidou
et al found that 29% of the students gave an explanation in which they explicitly employed
the ideas of energy being used up. In another study by Fetherston (1999), a much smaller
percentage of students (15%) erroneously stated that energy is used up during processes in
living things. A similar finding was documented by Kesidou et al (1993) and Fetherston
(1999) in which high school students had an erroneous view that energy is used up.
Energy Conservation
84
Scientifically, energy cannot be used up, instead, it remains constant despite the energy
changes which occur, according to the First Law of Thermodynamics. However, in everyday
language usage, energy is viewed as a substance which becomes used up in situations
dealing with activity such as exercises. Many students may erroneously conclude that
energy is used up, as in batteries which go flat or when food is eaten or during activities
(Kesidou et al, 1993; Fetherston, 1999).
4.2.2. Ideas relating to energy being built up when an organism is at rest or active
Two statements tested the idea that energy can be built up. Almost half of the students in the
sample (43%) erroneously indicated that the statement After exercise, you can build up your
energy levels by resting is correct, although 17 of them had doubts about whether their answer
was correct. However, quite a large number of the students (56% of them) correctly
indicated that the statement was scientifically incorrect; although very few of them (17) were
sure their response was correct. The majority (32) seemed to be unsure that their answer was
correct. When asked to underline the word/phrase that made the statement incorrect, nine
students correctly underlined the phrase build up as being erroneous. However, when it
came to writing-in the word/phrase to correct the statement, very few students did so. For
instance, only one student correctly wrote-in the phrase do not build up to correct the
statement.
The statement During exercise, energy is built up in the body, also tested whether students
agree that energy is built up. And 16% of them erroneously indicated that it was correct,
and six of them were sure of their answer. To the contrary, almost all students (82%) held a
scientists view that the statement was incorrect, and more than half of these students (47 of
them) were sure of their answer. When asked to underline the incorrect word/phrase in the
statement, 42 students recognised and underlined build up as an erroneous phrase.
However, only 7 students wrote-in an acceptable phrase converted to different forms to
correct the statement. The rest of the students still provided unacceptable phrases such as
used up (23 students) and lost (7 students). As explained earlier, the word lost contradicts the
principle of energy conservation, if there is no added explanation that heat energy is lost to
the body during respiration.
4.2.3. Ideas relating to energy not being required when a body is at rest
This claim was tested in the statement When you are asleep, your body does not require any
energy because it is not active. Very few students (7%) erroneously stated that the statement
was correct. To the contrary, nearly all students (92%) correctly identified the statement as
scientifically incorrect, and 71 of them were sure their response was correct. When asked to
underline the word/phrase which makes the statement wrong, 47 students correctly
underlined does not require any energy because it is not active. Of the 47 students, 21 of
them wrote in an acceptable phrase does require energy as it is still active and 8 other
students wrote in another acceptable phrase many body processes (e.g. respiration) still
occur to correct the statement. Most students in this study appeared to hold a scientifically
Understanding Energy Conservation: Intersection Between Biological and Everyday Life Contexts
85
acceptable view that the human body is active even at rest, and therefore energy is always
required.
4.2.4. Ideas relating to energy being lost when an organisms is active
Slightly more than half of the students in the sample (59%) erroneously indicated that the
statement When living things are active, they lose energy was correct, and 30 of them were sure
of their answer. On the other hand, 40% of them exhibited a scientific view that the
statement was incorrect, and more than half (20 of them) were sure of their answer. When
asked to underline an incorrect word in the statement, 25 students correctly underlined the
word lose, with 7 students writing in the acceptable phrase convert or transform energy
into different forms. However, 10 of 25 students who underlined the word lose
erroneously replaced it with an unacceptable phrase used up.
The idea that energy is lost during activity in living organisms was documented by
Solomon (1982). In everyday life experiences, people may well consider energy to be lost,
and that the amount of energy decreases, especially during and after exercises. As a
result, the scientific viewpoint that the amount of energy remains constant, despite the
transformations that occur (i.e. energy conservation) does not seem to be applied in
everyday experiences. According to the First Law of Thermodynamics (the law of
conservation of energy), energy cannot be created or destroyed, but it can be converted
from one form to another without any loss; any apparent loss of energy can be explained
as the conversion of energy into some other form (Solomon et al., 1993; Raven and
Johnson, 1999). For example, during each energy conversion in living systems, some of the
energy is used to drive the metabolic processes and some of it dissipates to the
atmosphere in the form of heat. When talking about energy, the idea of energy being lost
usually appears to be erroneous because it implies that energy is not conserved, although
energy in the form of heat certainly leaves the body.
4.2.5. Inability to apply the energy conservation principle to biological situations
Although nearly all students (98%) correctly stated the energy conservation principle
(energy cannot be created or destroyed) in test question 1, their ability to apply this concept
to biological situations proved otherwise, as shown in Tables 3 & 4. The contradictory
answers given to the closed statements could suggest that the students are unable to apply
the idea of energy conservation. This situation may suggest that students could have rote-
learned this principle or could have seen it in textbooks. Another source for this problem
could be the language differences between science and everyday usage. Using phrases such
as used up, build up or lost are not scientifically correct when talking about energy
conservation.
The inability to apply the scientific idea of energy conservation in biological systems among
students has also been identified by other researchers (e.g. Barak et al., 1997; Gayford, 1986;
Goldring & Osborne, 1994; Kesidou & Duit, 1993; Kruger et al., 1992; Linjse, 1990; Liu et al,
Energy Conservation
86
2002; Solomon, 1985; Trumper, 1997; Warren, 1986). For instance, Barak et al (1997)
conducted a study in which they found that majority of the students had difficulties in
applying the law of energy conservation in a biological context. Other researchers such as
Kesidou et al (1993) found that none of their 34 Grade Ten German students could apply the
idea of energy conservation. Similarly, even teachers have been found to have this problem
as documented by Kruger et al (1992) where majority of the answers teachers provided
contradicted with the principle of energy conservation.
In light of students inability to apply the concept of energy conservation, Warren (1986)
explained that the conservation of energy is problematic because it implies saving fuel when
used in everyday life and social understanding. In another explanation, Duit (1981) argued
that energy conservation may not be intelligible to most learners because in everyday usage,
energy is viewed to be produced and consumed, but not conserved (p. 292). The inability
of students in this study to consistently apply this principle may suggest that students could
have rote-learned this law or could have seen it in textbooks.
4.3. What happens to energy during metabolic processes in living organisms
Students responses on what happens to energy during metabolism are in Table 5.
What happens to energy during metabolic processes %
of Students
Statements to do with energy being created or degraded
Scientifically acceptable statement
Energy is neither created nor destroyed
Scientifically unacceptable statements
Energy is created/made during processes (e.g. photosynthesis & respiration)
in organisms
Energy is degraded during processes
55
40
9
6
Statements to do with energy used up & lost during processes
Scientifically unacceptable statements
Energy is used up during processes (e.g. respiration) in living organisms
Energy is lost during an activity (e.g. exercises) in organisms
37
27
10
Statements to do with energy being transformed or transferred
Scientifically acceptable statement
Energy can be transformed or converted from one form to another
7
7
Table 5. Students responses on what happens to energy during metabolic processes
Understanding Energy Conservation: Intersection Between Biological and Everyday Life Contexts
87
4.3.1. Ideas relating to energy being created or degraded in metabolic processes
Forty percent of the students correctly stated that energy is neither created nor destroyed
during metabolic processes. However, these students did not go further to explain what
happens to the energy - a situation which may suggest that they lack an understanding of
energy transformation and transfer. On the other hand, some students erroneously stated
that during metabolic processes, energy is created (9%) or degraded (6%).
In support of our findings, some researchers have documented that an erroneous idea of
energy being created during biological processes persists among students. For instance,
Eisten et al (1988) found that 3% of the biology majors and 4% of the non-biology majors
provided answers which implied that energy is created during respiration. However, as
pointed out earlier, it is possible that in the case of some teachers or learners these are not
really erroneous ideas but imprecise use of language.
4.3.2. Ideas relating to energy being used up or lost during metabolic processes
Quite a large percentage of the students (37%) provided responses which suggested that
they erroneously believed energy is used up or lost during biological processes. That is, 27
% and 10% of the students erroneously wrote that energy is used up during processes and
energy is lost during an activity in organisms, respectively. These findings add to the
contradictory responses provided by these students to the closed-ended statements in
Tables 3 and 4. Similar findings were documented in previous studies (e.g. Solomon, 1982;
Linjse, 1990; Kesidou et al, 1993; Fetherston, 1999).
4.3.3. Ideas relating to energy conversion during metabolic processes
The idea of energy transformation or conversion is loosely understood by nearly all students
in this study. That is, only 7% of the students correctly indicated that energy is transformed
from one form to another during metabolic processes. Similarly, Mann (2003) also found
that many students had poor understanding of energy conversion and transfer.
5. Implications for teaching and learning about energy conservation
The answers provided by students suggest that majority of them have an incomplete
understanding of energy conservation in biological contexts. The question which then arises
is: What should be done about the problems students have in understanding the biological-
context energy conservation? There are several potential areas in which biology educators
can get involved, if problems faced by students are to be minimised. First, it is important
that teachers identify students prior ideas before starting to teach energy conservation (e.g.
Driver, et al, 1994; Fetherston, 1999; Solomon, 1982). This is because this concept has
everyday life understandings which may conflict with those of science a situation which
can make students responses scientifically incorrect. One possible way to do this is by using
diagnostic strategies that uses every day and familiar contexts in order to help students
Energy Conservation
88
understand the scientific viewpoints. By contrast, teaching energy conservation in terms that
do not relate to familiar experiences may not be meaningful to learners a situation which
was triangulated in this study where students provided the textbook definition of energy
conservation, but could not apply it to statements involving biological phenomena.
Second, we recommend that teachers explain why certain words such as used up, built up,
created, or lost are unacceptable when talking about energy, since many students had
problems with the energy conservation principle. It is hoped that if science teachers
introduce and discuss the erroneous words or phrases, it may serve as a basis for alerting
students to the problems involved in using them.
Third, there seemed to be a lack of understanding among many students that energy is not
lost, but transformed to various forms during metabolic processes. Therefore, the concept of
energy transformation could be one of the ideas which biology teachers could emphasize
more when teaching about energy conservation. In this regard, we believe the use of the
phrase energy is used up should be discouraged instead we recommends the phrase
energy is transformed or transferred. In addition other researchers such as Lee and Liu (2010)
recommend that the teaching of energy and energy conservation be based on the knowledge
integration approach (defined as students knowledge and ability to elicit and connect
scientifically normative and relevant ideas in explaining a scientific phenomenon or
justifying their claim in a scientific problem), which takes into account the energy source,
energy transformation, and energy conservation.
As stated by Gilbert et al., (1982), one of the unintended learning outcomes which results
when students prior ideas are not appropriately dealt with, is that students stick to their
own prior ideas in spite of teaching. This trend was evident in this study as students
provided conflicting answers to the closed statements. Therefore, one practical approach to
teach this concept is by providing students with a variety of situations, experiences and
activities when teaching in order to overcome the usual conceptual reductionism. Since
energy conservation principle is not intelligible to most learners, their understanding would
be enhanced if the learning activities are based in contexts in which students construct their
knowledge, particularly across science disciplines (i.e. biology, chemistry and physics) and
everyday life contexts.
6. Recommendations for future research
Although identifying incorrect answers and ideas is a vital step in improving
understanding, it is important that reasons for the incorrect ideas are understood. Thus,
further research focussing on why students provide incorrect ideas is recommended. In
particular, the researcher(s) would find out why students use phrases such as used up, lost,
built up, created, when talking about energy conservation. Perhaps, this would lead to a step
further in which the researcher could consider the extent to which everyday language and
experiences interfere in the understanding of energy conservation. Secondly, some
researchers (e.g. Lee, 2011) have advocated for a set of energy literacy to become the basis
Understanding Energy Conservation: Intersection Between Biological and Everyday Life Contexts
89
for further curriculum development and instructional design in schools. Therefore, research
aimed at compiling what should constitute energy literacy is required.
7. Conclusion
Although energy conservation is considered an ease concept for students to recite as shown
in our study, majority of the students have problems applying it to biological systems. For
instance, our study revealed two major aspects. First, whilst nearly all students (98%)
correctly stated the energy conservation principle (i.e. energy cannot be created or destroyed to
be correct), majority of them could not apply it consistently to other statements testing the
same concept. Second, many students erroneously indicated the energy is lost, used up,
build up during metabolic processes in organisms. These findings suggest that even if
students could state the energy conservation principle, they may in fact not have a
conceptual understanding of the concept. However, one point to note is that some answers
which were wrong could have been a reflection of language problems and not conceptual
problems. Since energy is an important concept that concerns our daily life, students
mistakes in language usage can have detrimental influence on the scientific comprehension
of the energy conservation principle. The language problem as a confounding variable in the
diagnosis of students understanding has been discussed by Clerk and Rutherford (2000,
715) when they stated that:
Language problems do sometimes masquerade as misconceptions. This has serious implications for
teaching. If a student is found to be answering questions incorrectly, it could be counter-productive to
jump to conclusion that true misconceptions are held.
Therefore, the teaching and learning of energy conservation should be based on diagnosing
students language usage, and by using various contexts such as everyday life examples.
Doing so would consequently ensure a complete understanding of the energy conservation
principle in biological systems.
Author details
Vivien Mweene Chabalengula and Frackson Mumba
Southern Illinois University Carbondale, USA
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Section 2
Applications of Energy Conservation
Chapter 4
Hydro Power
Mohammed Taih Gatte and Rasim Azeez Kadhim
Additional information is available at the end of the chapter
http://dx.doi.org/10.5772/52269
1. Introduction
Humans have used the power of flowing water for thousands of years. Early civilizations
used wooden paddle wheels to grind corn and wheat to flour. The word Hydro comes from
the Greek word for water. Hydropower traditionally represents the energy generated by
damming a river and using turbine systems to generate electrical power. However, there are
several other ways we can generate energy using the power of water. Ocean waves, tidal
currents and ocean water temperature differences can all be harnessed to generate energy.
More than 70 percent of the earth is covered by water. The United States is one of the worlds
top producers of hydropower (see chart). As much as 12 percent of the electrical energy
generated in the U.S. is currently derived from hydropower systems. Parts of the Pacific
Northwest generate as much as 70 percent of their electricity using hydroelectric sources.
More than half the renewable energy generated in the United States comes from
hydroelectric dams. Hydroelectric power is currently the least expensive source of electrical
power and is much cleaner than power generated using fossil fuels.
Figure 1. The amount of annual hydro electric energy of different countries.
Energy Conservation 96
Flowing and falling water have potential energy. Hydropower comes from converting
energy in flowing water by means of a water wheel or through a turbine into useful
mechanical power. This power is converted into electricity using an electric generator or is
used directly to run milling machines. The potential energy of water may be used directly
without conversion operation because of different in elevation diverted the water through a
pipelines in order to supply the water in the daily usage .
2. History of hydro power
In the ancient times waterwheels were used extensively, but it was only at the beginning of
the 19th Century with the invention of the hydro turbines that the use of hydropower got
popularized. Small-scale hydropower was the most common way of electricity generating in
the early 20
th
century. The first commercial use of hydroelectric power to produce electricity
was a waterwheel on the Fox River in Wisconsin in 1882 that supplied power for lighting of
two paper mills and a house. Within a matter of weeks for this installation, a power plant
was also put into commercial service at Minneapolis1. India has a century old history of
hydropower and the beginning was from small hydro. The first hydro power plant was of
130 kW set up in Darjeeling during 1897, marked the development of hydropower in the
country. Similarly, by 1924 Switzerland had nearly 7000 small scale hydropower stations in
use. Even today, Small hydro is the largest contributor of electricity from renewable energy
sources, both at European and world level. With the advancement of technology, and
increasing requirement of electricity, the thrust of electricity generation was shifted to large
size hydro and thermal power stations.
However, it is only during the last two decades that there is a renewed interest in the
development of small hydro power (SHP) projects mainly due to its benefits particularly
concerning environment and ability to produce power in remote areas. Small hydro
projects are economically viable and have relatively short gestation period. The major
constraints associated with large hydro projects are usually not encountered in small
hydro projects. Renewed interest in the technology of small scale hydropower actually
started in China which has more than 85,000 small-scale, electricity producing,
hydropower plants.
Hydropower will continue to play important role throughout the 21st Century, in world
electricity supply. Hydropower development does have some challenges besides the
technical, economic and environmental advantages it shares above other power generation
technologies.
At the beginning of the new Millennium hydropower provided almost 20% (2600 TWh/year)
of the electricity world consumption (12900 TWh/year). It plays a major role in several
countries. According to a study of hydropower resources in 175 countries, more than 150
have hydropower resources. For 65 of them, hydro produces more than 50% of electricity;
for 24, more than 90% and 10 countries have almost all their electricity requirements met
through hydropower.
Hydro Power 97
3. Hydro power system classification
A different countries have different criteria to classify hydro power plants, a general
classification of hydro power plants is as follows in table 1 :
Capacity in KW Type
Up to 100 Micro Hydro
101 to 2000 Mini Hydro
2001 to 25000 Small Hydro
> 25000 Large Hydro
Table 1. The hydro power types according to output power
The hydro plants are also classified according to the Head or the vertical distance through
which the water is made to impact the turbines. The usual classifications are given in table
2. below:
Head Range Type
100 m and above High head
30 100 m Medium head
2 30 m Low head
Table 2. The hydro power types according to head
These ranges are not rigid but are merely means of categorizing sites. Schemes can also be
defined as:
Run-of-river schemes
Schemes with the powerhouse located at the base of a dam
Schemes integrated on a canal or in a water supply pipe
Most of small hydro power plants are run-of-river schemes, In order to imply that they do
not have any water storage capability. The power is generated only when enough water is
available from the river/stream. When the stream/river flow reduces below the design flow
value, the generation ceases as the water does not flow through the intake structure into the
turbines. Small hydro plants may be stand alone systems in isolated areas/sites, but could
also be grid connected (either local grids or regional/national grids). The connection to the
grid has the advantage of easier control of the electrical system frequency of the electricity,
but has the disadvantage of being tripped off the system due to problems outside of the
plant operators control.
Energy Conservation 98
4. The hydro power principles
Power generation from water depends upon a combination of head and flow. Both must
be available to produce electricity. Water is diverted from a stream into a pipeline, where
it is directed downhill and then through the turbine (flow). The vertical drop (head)
creates pressure at the bottom end of the pipeline. The pressurized water emerging from
the end of the pipe creates the force that drives the turbine. The turbine in turn drives the
generator where electrical power is produced. More flow or more head produces more
electricity. Electrical power output will always be slightly less than water power input
due to turbine and system inefficiencies. Water pressure or Head is created by the
difference in elevation between the water intake and the turbine. Head can be expressed
as vertical distance (feet or meters), or as pressure, such as pounds per square inch (psi).
Net head is the pressure available at the turbine when water is flowing, which will always
be less than the pressure when the water flow is turned off (static head), due to the
friction between the water and the pipe. Pipeline diameter also has an effect on net head.
Flow is quantity of water available, and is expressed as volume per unit of time, such as
gallons per minute (gpm), cubic meters per second (m
3
/s), or liters per minute (lpm).
Design flow is the maximum flow for which the hydro system is designed. It will likely be
less than the maximum flow of the stream (especially during the rainy season), more than
the minimum flow, and a compromise between potential electrical output and system
cost. The theoretical power (P) available from a given head of water is in exact proportion
to the head and the quantity of water available.
P= Q H e 9.81 kW
Where
P Power at the generator terminal, in kilowatts (kW)
H The gross head from the pipeline intake to the tail water in meters (m)
Q Flow in pipeline, in cubic meters per second (m
3
/s)
e The efficiency of the plant, considering head loss in the pipeline and the efficiency of
the turbine and generator, expressed by a decimal (e.g. 85% efficiency= 0.85)
9.81 is a constant and is the product of the density of water and the acceleration due to
gravity (g)
Example: A site has a head of 100 m with flow of 0.1 m
3
/s .calculate the output power
output if a) e=100% , b) e=50% .
Solution:
a. P = 100 * 0.1 * 9.81 * 100% = 98.1 KW
b. P = 100 * 0.1 * 9.81 * 50% = 49 KW
Table 3. below shows the output power (KW) with ( e = 50%) for different heads and flows
Hydro Power 99
Flow Rates (m
3
/s)
Head
(m)
2.0 1.0 0.5 0.2 0.1 0.08 0.04 0.02 0.01
Output Power in (KW)
980 490 245 98 49 39.2 19.6 9.8 4.9 1
1960 980 490 196 98 78.4 39.2 19.6 9.8 2
3920 1960 980 392 196 156.8 78.4 39.2 19.6 4
7840 3920 1960 784 392 313.6 156.8 78.4 39.2 8
9800 4900 2450 980 490 392 196 98 49 10
14700 7350 3675 1470 735 588 294 147 73.5 15
19600 9800 4900 1960 980 784 392 196 98 20
29400 14700 7350 2940 1470 1176 588 294 147 30
39200 19600 9800 3920 1960 1568 784 392 196 40
49000 24500 12250 4900 2450 1960 980 490 245 50
98000 49000 24500 9800 4900 3920 1960 980 490 100
147000 73500 36750 14700 7350 5880 2940 1470 735 150
196000 98000 49000 19600 9800 7840 3920 1960 980 200
Table 3. Table 3. the output hydro power with different heads and flow rates
5. Basic components of a hydropower system
Figure 2 below shows the major components of a typical hydropower scheme. The water in
the river is diverted by the weir through an opening in the river side (the intake) into a
channel (this could be open or buried depending upon the site conditions). A settling basin is
built in to the channel to remove sand and silt from the water. The channel follows the contour
of the area so as to preserve the elevation of the diverted water. The channel directs the water
into a small reservoir/tank known as the forebay from where it is directed on to the turbines
through a closed pipe known as the penstock. The penstock essentially directs the water in a
uniform stream on to the turbine at a lower level. The turning shaft of the turbine can be used
to rotate a mechanical device (such as a grinding mill, oil expeller, wood lathe, etc.) directly, or
to operate an electricity generator. The machinery or appliances which are energized by the
turbine are called the load. When electricity is generated, the power house where the
generator is located transfers the electricity to a step-up transformer which is then
transmitted to the grid sub-station or to the village/area where this electricity is to be used.
Energy Conservation 100
Figure 2. The hydro power plant components
5.1. Civil works
Civil works structures control the water that runs through a hydropower system, and
conveyances are a large part of the project work. It is important that civil structures are
located in suitable sites and designed for optimum performance and stability. Other factors
should be considered in order to reduce cost and ensure a reliable system, including the use
of appropriate technology, the best use of local materials and local labour, selection of cost-
effective and environmentally friendly structures, landslide-area treatment and drainage-
area treatment. Head works consist of the weir (see Figure 2 ), the water intake and
protection works at the intake to safely divert water to the headrace canal. At some sites you
may be able to install the penstock directly in the intake, with no need for a canal.
A hydropower station essentially needs water to be diverted from the stream and brought to
the turbines without losing the elevation/head. Given below are some of the important
factors that must be kept in mind while designing a hydropower system: Available head:
The design of the system has effects on the net head delivered to the turbine. Flow
variations: The river flow varies during the year but the hydro installation is designed for
almost a constant flow. Sediment: Flowing water in the river sometimes carry small
particles of hard abrasive matter (sediment) which can cause wear to the turbine if they are
not removed before the water enters the penstock. Floods: Flood water will carry larger
suspended particles and will even cause large stones to roll along the stream bed.
Turbulence: In all parts of the water supply line, including the weir, the intake and the
channel, sudden alterations to the flow direction will create turbulence which erodes
structures and causes energy losses. Most common civil structures used in a hydro power
scheme are:
Hydro Power 101
5.1.1. Weir and intake
A hydro power system necessitates that water from the river to be diverted and extracted
in a reliable and controllable manner. The water flowing in the channel must be regulated
during high river flow and low flow conditions. A weir can be used to raise the water
level and ensure a constant supply to the intake. Sometimes it is possible to avoid
building a weir by using natural features of the river. A permanent pool in river could
also act as a weir.
Another condition in site selection of the weir is to protect it from damage. Sometimes, in
remote hilly regions, where annual flooding is common it may be prudent to build
temporary weir using local resources and manpower. The temporary weir is a simple
structure at low cost using local labour, skills and materials. It is expected to be destroyed
by annual or bi-annual flooding. However, advanced planning has to be done for rebuilding
of the weir.
The intake of a hydro power is designed to divert only a portion of the stream flow or the
complete flow depending upon the flow conditions and the requirement. Hydro power
schemes use different types of intakes distinguished by the method used to divert the water
into the intake. For hydro power schemes, intake systems are smaller and simpler. The
following three types of intakes have been described here: side intake with and without a
weir and the bottom intake. The advantages and disadvantages associated with each of
these are given in the table below:
Attributes Side intake without weir Side intake with weir Bottom intake
Advantages 1. Relatively cheap
2. No complex machinery
required for construction
1. Control over water
level
2. Little maintenance
necessary (if well
designed)
1. Very useful at
fluctuating flows. Even
the lowest flow can be
diverted.
2. No maintenance
required (if well
designed)
Dis-
advantages
1. Regular maintenance
and repairs required.
2. At low flows very little
water will be diverted
and therefore this type of
intake is not suitable for
rivers with great
fluctuations in flow.
1. Low flow cannot be
diverted properly
2. Modern materials like
concrete necessary.
1. Expensive.
2. Local materials not
suitable.
3. Good design required
to prevent blockage by
sediment.
Table 4. The advantages and disadvantages of the intake types
Energy Conservation 102
5.1.2. Power channels
The power channel or simply a channel conducts the water from the intake to the forebay
tank. The length of a channel depends upon the topography of the region and the distance
of powerhouse from the intake. Also the designing of the MHP systems states the length of
the channel sometimes a long channel combined with a short penstock can be cheaper or
required, while in other cases a combination of short channel with long penstock would be
more suitable.
In the Himalayan region, the hydro power channels are sometimes as long as a few
kilometers to create a head of 10 to 60 meters or more. Generally power channels are
excavated and to reduce friction and prevent leakages these are often lined with cement,
clay or polythene sheet. Size and shape of a channel and material used for lining are often a
dictated by cost and head considerations. During the process of flowing past the walls and
bed material, the water loses energy. The rougher material have greater friction loss and
higher elevation difference needed between channel entry and exit.
In hilly regions it is common that the power channel would have to cross small streams. In
such situations it is often prudent to build a complete crossing over the channel, during
rainy season and flash floods, rocks/mud may block the channel or wash away sections of
the channel. Sometimes just the provision of a drain running under the channel (in case of
very small streams along stable slopes) is usually adequate. The power channel has some
important parts which are described in the sub-sections below:
5.1.3. Settling basin
The water diverted from the stream and carried by the channel usually carries a suspension
of small particles such as sand that are hard and abrasive and can cause expensive damage
and rapid wear to turbine runners. To get rid of such particles and sediments, the water
flow is allowed to slow down in settling basins so that the sand and silt particles settle on
the basin floor. The deposits are then periodically flushed. The design of settling basin
depends upon the flow quantity, speed of flow and the tolerance level of the turbine
(smallest particle that can be allowed). The maximum speed of the water in the settling
basin can thus be calculated as slower the flow, lower is the carrying capacity of the water.
The flow speed in the settling basin can be lowered by increasing the cross section area.
5.1.4. Spillways
Spillways along the power channel are designed to permit overflow at certain points along
the channel. The spillway acts as a flow regulator for the channel. During floods the water
flow through the intake can be twice the normal channel flow, so the spillway must be large
enough to divert this excess flow. The spillway can also be designed with control gates to
empty the channel. The spillway should be designed in such a manner that the excess flow
is fed back without damaging the foundations of the channel.
Hydro Power 103
Figure 3. Spillway of Darbandikhan dam
5.1.5. Forebay tank
The forebay tank serves the purpose of providing steady and continuous flow into the
turbine through the penstocks. Forebay also acts as the last settling basin and allows the last
particles to settle down before the water enters the penstock. Forebay can also be a reservoir
to store water depending on its size (large dams or reservoirs in large hydropower schemes
are technically forebay).
A sluice will make it possible to close the entrance to the penstock. In front of the penstock a
trashrack need to be installed to prevent large particles to enter the penstock. A spillway
completes the forebay tank.
Figure 4. Forebay tank
Energy Conservation 104
5.2. Penstock
The penstock pipe transports water under pressure from the forebay tank to the turbine,
where the potential energy of water is converted into kinetic energy in order to rotate the
turbine. The penstock is often the most expensive item in the project budget as much as 40
percent is not uncommon in high-head installations. It is therefore worthwhile to optimize
its design in order to minimize its cost. The choice of size and type of penstock depends on
several factors that are explained briefly in this section. Basically, the trade-off is between
head loss and capital cost.
Head loss due to friction in the penstock pipe depends principally on the velocity of water,
the roughness of pipe wall and the length and diameter of pipe. The losses decrease
substantially with increased pipe diameter. Conversely, pipe costs increase steeply with the
increase of diameter. Therefore, a compromise between cost and the required performance.
The design philosophy is first identify available pipe options, select a target head loss of 5 to 10
percent or less of the gross head, and keep the length as short as possible. Several options for
sizes and types of materials may need to be calculated and evaluated in order to find a suitable
penstock pipe. A smaller penstock may save on capital costs, but the extra head loss may
account for lost energy and revenue from generated electricity (if you are selling the power). In
smaller systems, the allowable head loss can be as much as 33 percent. This is particularly
relevant to developers who combine domestic water supply and penstock in the same pipe.
Several factors should be considered when deciding which material will be used in a
particular penstock: design pressure, the roughness of the pipes interior surface, method of
joining, weight and ease of installation, accessibility to the site, design life and maintenance,
weather conditions, availability, relative cost and likelihood of structural damage.
The pressure rating of the penstock is critical because the pipe wall must be thick enough to
withstand the maximum water pressure; otherwise there will be a risk of bursting. The
pressure of the water in the penstock depends on the head; the higher head is higher
pressure. Pressure ratings are normally given in bar units or PSI; 10.2 m of head will exert a
pressure of 1 bar, or 14.5 PSI. The penstock becomes more expensive as the pressure rating
increases.
The most commonly used materials for a penstock are HDPE, uPVC and mild steel because
of their suitability, availability and affordability. Layout of the penstock pipelines depends
on their material, the nature of terrain and environmental considerations; they are generally
surface-mounted or buried underground. Special attention is necessary where a penstock is
installed in a very cold environment; protection from ice and frost must be considered. In
severe frost areas, penstocks should always be buried below the frost line. Where freezing is
not a concern, the penstock may be left above ground. However, it is generally preferable to
bury the penstock to provide protection from expansion, animals and falling trees. Because
of changes in the ambient temperature, the length of the penstock pipe may be subjected to
expansion and contraction. Expansion joints are used to compensate for maximum possible
changes in length.
Hydro Power 105
Material Friction Weight Corrosion Cost Jointing Pressure
Mild Steel XXX XXX XXX XXXX XXXX XXXXX
HDPE
2
XXXXX XXXXX XXXXX XX XX XXXXX
uPVC
3
XXXXX XXXXX XXXX XXXX XXXX XXXXX
1
Adapted from Frankel, Peter , et al. Micro-Hydro Power : A Guide for development Workers . London, U.K:
Intermediate Technology Publications in association with the Stockholm Environment Institute , 1991.
X = Poor ------------- XXXXX = Excellent
2
HDPE = High density polyethylene
3
uPVC = Unplastified polyvinyl chroride
Table 5. Comparison of Penstock Materials
1
The hydrostatic pressure created from the head must be determined so that a suitable wall
thickness can be determined. This pressure is given by Equation (1).
Pressure = p*g*H
(1)
p density of water
g acceleration due to gravity
H head
With the pressure calculated, the minimal wall thickness can then be calculated from
Equation (2).
t = P*D / 2*s
(2)
t wall thickness
P hydrostatic pressure
D diameter
s allowable tensile stress
Friction is always present, even in fluids, it is the force that resists the movement of objects.
When you move a solid on a hard surface, there is friction between the object and the
surface. If you put wheels on it, there will be less friction. In the case of moving fluids such
as water, there is even less friction but it can become significant for long pipes. Friction can
be also be high for short pipes which have a high flow rate and small diameter as in the
syringe example. In fluids, friction occurs between fluid layers that are traveling at different
velocities within the pipe (see Figure 5). There is a natural tendency for the fluid velocity to
be higher in the center of the pipe than near the wall of the pipe. Friction will also be high
for viscous fluids and fluids with suspended particles.
Another cause of friction is the interaction of the fluid with the pipe wall, the rougher pipe
has higher friction. Friction depends on:
- average velocity of the fluid within the pipe
- viscosity
- pipe surface roughness
Energy Conservation 106
the increase in any one of these parameters will increase friction. The amount of energy
required to overcome the total friction loss within the system has to be supplied by the
pump if you want to achieve the required flow rate. In industrial systems, friction is not
normally a large part of a pump's energy output. For typical systems, it is around 25% of the
total. If it becomes much higher then you should examine the system to see if the pipes are
too small. However all pump systems are different, in some systems the friction energy may
represent 100% of the pump's energy, this is what makes pump systems interesting, there is
a million and one applications for them. In household systems, friction can be a greater
proportion of the pump energy output, maybe up to 50% of the total, this is because small
pipes produce higher friction than larger pipes for the same average fluid velocity in the
pipe . Another cause of friction are the fittings (elbows, tees, y's, etc) required to get the fluid
from point to point. Each one has a particular effect on the fluid streamlines. For example in
the case of the elbow , the fluid streamlines that are closest to the tight inner radius of the
elbow lift off from the pipe surface forming small vortexes that consume energy. This
energy loss is small for one elbow but if you have several elbows and other fittings it can
become significant. Generally, they rarely represent more than 30% of the total friction due
to the overall pipe length.
To sum up, head losses in a penstock depend on:
Its shape: singularities as elbows or forks tend to increase head losses
Its internal diameter
Its wall roughness and its evolution due to its degradation or/ and to wall deposits.
It may be recalled here that energy loss due to friction in a penstock can be estimated as
being inversely proportional to its diameter to the power of five. For instance, a diameter
increase of 20% leads to a head losses decrease of 60%. Figure 5. shows the relation between
the head loss (feet ) with the flow rate (gpm) for a 100 feet PVC class 160 plastic pipe.
Figure 5. The relation of head loss with the flow
Hydro Power 107
5.3. Turbines
Turbine is the main piece of equipment in the hydro power scheme that converts energy of
the falling water into the rotating shaft power. The selection of the most suitable turbine for
any particular hydro site depends mainly on two of the site characteristics head and flow
available. All turbines have a power-speed characteristic. This means they will operate most
efficiently at a particular speed, head and flow combination. Thus the desired running speed
of the generator or the devices being connected/ loading on to the turbine also influence
selection. Other important consideration is whether the turbine is expected to generate
power at part-flow conditions. The design speed of a turbine is largely determined by the
head under which it operates. Turbines can be classified as high head, medium head or low
head machines. They are also typified by the operating principle and can be either impulse
or reaction turbines. The basic turbine classification is given in the table below:
Turbine Runner High Head Medium Head Low Head Ultra- Low Head
Impulse Pelton
Turgo
Cross- flow
Turgo
Muti-jet Pelton
Cross- flow
Multi jet
Turgo
Water wheel
Reaction - Francis
Pump- as
turbine
Propeller
Kaplan
Propeller
Kaplan
Table 6. Groups of water Turbines
The rotating part (called runner) of a reaction turbine is completely submerged in water
and is enclosed in a pressure casing. The runner blades are designed in a manner such that
the pressure difference across their surface imposes lift forces (similar to the principle used
for airplane wings) which cause the runner to turn/rotate.
The impulse turbine (as the name suggests) on the other hand is never immersed in water
but operates in air, driven by a jet (or jets) of water striking its blades. The nozzle of the
penstock converts the head of the water (from forebay tank) into a high speed jet that hits
the turbine runner blades that deflect the jet so as to utilize the change of momentum of the
water and converting this as the force on the blades enabling it to rotate.
Impulse turbines are usually cheaper than reaction turbines because there is no need for a
pressure casing nor for carefully engineered clearances, but they are also only suitable for
relatively higher heads.
5.3.1. Impulse turbines
Impulse turbines are more widely used for micro-hydro applications as compared to
reaction turbines because they have several advantages such as simple design (no pressure
seals around the shaft and better access to working parts - easier to fabricate and maintain),
greater tolerance towards sand and other particles in the water, and better part-flow
efficiencies. The impulse turbines are not suitable for low head sites as they have lower
Energy Conservation 108
specific speeds and to couple it to a standard alternator, the speed would have to be
increased to a great extent. The multi-jet Pelton, crossflow and Turgo turbines are suitable
for medium heads.
5.3.1.1. Pelton turbine
A Pelton turbine consists of a set of specially shaped buckets mounted on a periphery of a
circular disc. It is turned by forced jets of water which are discharged from one or more
nozzles and impinge on the buckets. The resulting impulse spins the turbine runner,
imparting energy to the turbine shaft. The buckets are split into two halves so that the
central area does not act as a dead spot incapable of deflecting water away from the
oncoming jet.
Figure 6. Pelton Turbine
The cutaway on the lower lip allows the following bucket to move further before cutting off
the jet propelling the bucket ahead of it and also permits a smoother entrance of the bucket
into the jet. The Pelton bucket is designed to deflect the jet through 165 degrees which is the
maximum angle possible without the return jet interfering with the following bucket for the
oncoming jet. They are used only for sites with high heads ranging from 60 m to more than
1000 m.
5.3.1.2. Turgo impulse turbines
The Turgo turbine is an impulse turbine designed for medium head applications. These
turbines achieve operational efficiencies of up to 87%. Developed in 1919 by Gilkes as a
modification of the Pelton wheel, the Turgo has certain advantages over Francis and Pelton
designs for some applications. Firstly, the runner is less expensive to make than a Pelton
wheel while it does not need an airtight housing like the Francis turbines. Finally the Turgo
has higher specific speeds and at the same time can handle greater quantum of flows than a
Pelton wheel of the similar diameter, leading to reduced generator and installation cost.
Turgo turbines operate in a head range where the Francis and Pelton overlap. Turgo
installations are usually preferred for small hydro schemes where low cost is very
important.
Turgo turbine is an impulse turbine where water does not change pressure but changes
direction as it moves through the turbine blades. The water's potential energy is converted
to kinetic energy with a penstock and nozzle. The high speed water jet is then directed on
Hydro Power 109
the turbine blades which deflect and reverse the flow and the water exits with very little
energy. Like all turbines with nozzles, blockage by debris must be prevented for effective
operation. A Turgo runner looks like a Pelton runner split in half. For the same power, the
Turgo runner is one half the diameter of Pelton runner, and so twice the specific speed. e
Turgo can handle a greater water flow than Pelton because exiting water doesn't interfere
with adjacent buckets.
The specific speed of Turgo runners is between the Francis and Pelton. Single or multiple
nozzles can be used. Increasing the number of jets increases the specific speed of the runner
by the square root of the number of jets i.e., four jets yield twice the specific speed of one jet
on the same turbine.
Figure 7. Turgo Turbine
5.3.1.3. Crossflow turbine
Also called a Michell-Banki turbine a crossflow turbine has a drum-shaped runner
consisting of two parallel discs connected together near their rims by a series of curved
blades. A crossflow turbine always has its runner shaft horizontal (unlike Pelton and Turgo
turbines which can have either horizontal or vertical shaft orientation). Unlike most water
turbines, which have axial or radial flows, in a crossflow turbine the water passes through
the turbine transversely, or across the turbine blades. As with a waterwheel, water enters at
the turbine's edge. After passing the runner, it leaves on the opposite side. Going through
the runner twice provides additional efficiency. When the water leaves the runner, it also
helps clean the runner of small debris and pollution. The cross-flow turbines generally
operate at low speeds. Crossflow turbines are also often constructed as two turbines of
different capacity that share the same shaft. The turbine wheels are the same diameter, but
different lengths to handle different volumes at the same pressure. The subdivided wheels
are usually built with volumes in ratios of 1:2. The subdivided regulating unit (the guide
vane system in the turbine's upstream section) provides flexible operation, with , or
100% output, depending on the flow. Low operating costs are obtained with the turbine's
relatively simple construction. The water flows through the blade channels in two
directions: outside to inside, and inside to outside. Most turbines are run with two jets,
Energy Conservation 110
arranged so that the two water jets in the runner will not affect each other. It is, however,
essential that the turbine, head and turbine speed are harmonized. The turbine consists of a
cylindrical water wheel or runner with a horizontal shaft, composed of numerous blades
(up to 37), arranged radially and tangentially. The edge of the blades are sharpened to
reduce resistance to the flow of water. A blade is made in a part-circular cross section (pipe
cut over its whole length). The ends of the blades are welded to disks to form a cage like a
hamster cage and are sometimes called "squirrel cage turbines"; instead of the bars, the
turbine has trough-shaped steel blades.
Figure 8. Crossflow Turbine
The water flows first from the outside of the turbine to its inside. The regulating unit,
shaped like a vane or tongue, varies the cross-section of the flow. These divide and direct
the flow so that the water enters the runner smoothly for any width of opening. The guide
vanes should seal to the edges of the turbine casing so that when the water is low, they can
shut off the water supply. The guide vanes therefore act as the valves between the penstock
and turbine. The water jet is directed towards the cylindrical runner by a fixed nozzle. The
water enters the runner at an angle of about 45 degrees, transmitting some of the water's
kinetic energy to the active cylindrical blades. The turbine geometry (nozzle-runner-shaft)
assures that the water jet is effective. The water acts on the runner twice, but most of the
power is transferred on the first pass, when the water enters the runner. Only of the
power is transferred to the runner when the water is leaving the turbine.
The crossflow turbine is of the impulse type, so the pressure remains constant at the runner.
The peak efficiency of a crossflow turbine is somewhat less than a Kaplan, Francis or Pelton
turbine. However, the crossflow turbine has a flat efficiency curve under varying load. With
a split runner and turbine chamber, the turbine maintains its efficiency while the flow and
load vary from 1/6
th
to the maximum. The crossflow turbines are mostly used in mini and
micro hydropower units less than 2 MW and with heads less than 200 m, since it has a low
price and good regulation. Particularly with small run-of-the-river schemes, the flat
efficiency curve yields better performance than other turbine systems, as flow in small
streams varies seasonally. The efficiency of a turbine is determined whether electricity is
produced during the periods when rivers have low heads. Due to its better performance
even at partial loads, the crossflow turbine is well-suited to stand-alone electricity
generation. It is simple in construction and that makes it easier to repair and maintain than
other turbine types. Another advantage is that the crossflow turbines gets cleaned as the
water leaves the runner (small sand particles, grass, leaves, etc. get washed away),
Hydro Power 111
preventing losses. So although the turbine's efficiency is somewhat lower, it is more reliable
than other types. Other turbine types get clogged easily, and consequently face power losses
despite higher nominal efficiencies.
5.3.2. Reaction turbines
The more popular reaction turbines are the Francis turbine and the propeller turbine.
Kaplan turbine is a unique design of the propeller turbine. Given the same head and flow
conditions, reaction turbines rotate faster than impulse turbines. This high specific speed
makes it possible for a reaction turbine to be coupled directly to an alternator without
requiring a speed-increasing drive system. This specific feature enables simplicity (less
maintenance) and cost savings in the hydro scheme. The Francis turbine is suitable for
medium heads, while the propeller is more suitable for low heads.
The reaction turbines require more sophisticated fabrication than impulse turbines because
they involve the use of larger and more intricately profiled blades together with carefully
profiled casings. The higher costs are often offset by high efficiency and the advantages of
high running speeds at low heads from relatively compact machines. Expertise and
precision required during fabrication make these turbines less attractive for use in micro-
hydro in developing countries. Most reaction turbines tend to have poor part-flow efficiency
characteristics
5.3.2.1. Francis turbine
The Francis turbine is a reaction turbine where water changes pressure as it moves through
the turbine, transferring its energy. A watertight casement is needed to contain the water
flow. Generally such turbines are suitable for sites such as dams where they are located
between the high pressure water source and the low pressure water exit. The inlet of a
Francis turbine is spiral shaped. Guide vanes direct the water tangentially to the turbine
runner. This radial flow acts on the runner's vanes, causing the runner to spin. The guide
vanes (or wicket gate) are adjustable to allow efficient turbine operation for a wide range of
flow conditions. As the water moves through the runner, its spinning radius decreases,
further delivering pressure acting on the runner. This, in addition to the pressure within the
water, is the basic principle on which the Francis turbine operates. While exiting the turbine,
water acts on cup shaped runner buckets leaving without any turbulence or swirl and hence
almost all of the kinetic or potential energy is transferred. The turbine's exit tube is shaped
to help decelerate the water flow and recover the pressure. Francis Turbine and generator
Guide vanes at minimum flow setting (cut-away view) Guide vanes at full flow setting(cut-
away view) Francis turbines can be designed for a wide range of heads and flows and along
with their high efficiency makes them one of the most widely used turbines in the world.
Large Francis turbines are usually designed specifically for each site so as to gain highest
levels of efficiencies (these are typically in the range of over 90%). Francis turbines cover a
wide range of head from 20 meters to 700 meters, and can be designed for outputs power
ranging from just a few kilowatts to one Gigawatt.
Energy Conservation 112
Figure 9. Francis Turbine
5.3.2.2. Kaplan turbine
The Kaplan turbine has adjustable blades and was developed on the basic platform
(design principles) of the Francis turbine by the Viktor Kaplan in 1913. The main
advantage of Kaplan turbines is its ability to work in low head sites which was not
possible with Francis turbines. Kaplan turbines are widely used in high-flow, low-head
power production.
The Kaplan turbine is an inward flow reaction turbine, which means that the working fluid
changes pressure as it moves through the turbine and gives up its energy. The design
combines radial and axial features. The inlet is a scroll-shaped tube that wraps around the
turbines wicket gate. Water is directed tangentially through the wicket gate and spirals on
to a propeller shaped runner, causing it to spin. The outlet is a specially shaped draft tube
that helps decelerate the water and recover kinetic energy.
The turbine does not need to be at the lowest point of water flow, as long as the draft tube
remains full of water. A higher turbine location, however, increases the suction that is
imparted on the turbine blades by the draft tube that may lead to cavitations due to the
pressure drop. Typically the efficiencies achieved for Kaplan turbine are over 90%, mainly
due to the variable geometry of wicket gate and turbine blades. This efficiency however may
be lower for very low head applications. Since the propeller blades are rotated by high-
pressure hydraulic oil, a critical design element of Kaplan turbine is to maintain a positive
seal to prevent leakage of oil into the waterway. Kaplan turbines are widely used
throughout the world for electrical power production. They are especially suited for the low
head hydro and high flow conditions mostly in canal based hydro power sites.
Inexpensive micro turbines can be manufactured for specific site conditions (e.g. for head as
low one meter). Large Kaplan turbines are individually designed for each site to operate at
the highest possible efficiency, typically over 90%. They are very expensive to design,
manufacture and install, but operate for decades.
Hydro Power 113
Figure 10. Kaplan Turbine
5.3.3. Turbine selection
Selection of an appropriate turbine to a large extent is dependent upon the available water
head and to a lesser extent on the available flow rate. In general, impulse turbines are used
for high head sites, and reaction turbines are used for low head sites. Kaplan turbines with
adjustable blade pitch are suitable for wide ranges of flow or head conditions, since their
peak efficiency can be achieved over a wide range of flow conditions. Small turbines (less
than 10 MW) may have horizontal shafts, and even fairly large bulb-type turbines up to 100
MW or so may be horizontal. Very large Francis and Kaplan machines usually have vertical
shafts because this makes best use of the available head, and makes installation of a
generator more economical. Pelton turbines may be installed either vertically or
horizontally.
Some impulse turbines use multiple water jets per runner to increase specific speed and
balance shaft thrust. Turbine type, dimensions and design are basically governed by the
following criteria:
Net head
Variation of flow discharge through the turbine
Rotational speed
Cavitation problems (quality of water available from penstock)
Cost
The main criterion considered in turbine selection is the net head. The figure given above
(Turbine Application Chart) specifies the range of operating heads for each turbine type.
The figure above and the table below show some overlapping, so that for a given head
several types of turbines can be used. The selection is particularly critical in low-head
schemes, where large discharges need to be handled to be economically viable.
Energy Conservation 114
Figure 11. Turbine Application Chart based on Head and Discharge
Turbine Type Typical range of heads (H = head in m)
Hydraulic wheel turbine 0.2 < H < 4
Archimedes' screw turbine 1 < H < 10
Kaplan & Propeller 2 < H < 40
Francis 10 < H < 350
Pelton 50 < H < 1300
Michell-Banki 3 < H < 250
Turgo 50 < H < 250
Table 7. The selection of turbine according to the head
5.3.4. Turbine efficiency
A significant factor in the comparison of different turbine types is their relative
efficiencies both at their design point and at reduced flows. Typical efficiency curves are
shown in the figure below. An important point to note is that the Pelton and Kaplan
turbines retain very high efficiencies when running below design flow; in contrast the
efficiency of the Crossflow and Francis turbines falls away more sharply if run at below
half their normal flow. Most fixed-pitch propeller turbines perform poorly except above
80% of full flow.
Hydro Power 115
Figure 12. Efficiency of Various Turbines based on Discharge rate
6. Hydro power in Iraq
In Iraq there are two big rivers (Tigris& Euphrates ) where a many dams are built, that
gives the ability to establish a hydro electric power plants on these dams such as ( mousal ,
hadeetha , samara , diala ,dokhanetc ) , which are distributed on the map below.
Figure 13. The distribution map of Dams in Iraq
Energy Conservation 116
Most of these dams have been used in the generation of electricity by building a hydro
electric power plants on it and the output power of these plant in Iraq are shown in table 6
below. The total generated power in Iraq is about 10171.5 MW as we see from this table
the hydro power generated is about 2489 Mw which represent a (25%) the amount of
hydroelectric power generated in Iraq varies according to the incoming quantity of water
that enter from these rivers.
Name of hydro power plant
Generated power output
( Mw )
Mosul 1050
Hadeetha 60
Hindia 15
Dukhan 400
Al- Kufa 5
Hmreen Dam 50
Samaraa 84
Al- Qadssia 660
Darbandikhan 240
Table 8. Hydro power plants in Iraq
6.1. Hydropower transportation and power conservation
In order to achieve the maximum (optimum) utilization of water and hydropower of the
rivers in Iraq we study and calculate the elevation of water at the dams in the whole
country such as (Hadeetha, Samara, Diala, Hindia, Kufa and Abasia .etc) and the
elevation of the middle and south province center (Baghdad, Basra, Babylon, Kut, Nasria,
Missan, and Samawa), by using the Google Earth program and then calculate the difference
in elevation. Figure (14) shows the map of the region of study.
Since the incoming water to Iraq was decrease last years and the high demand on the water
and electricity, the concentration of study was on the water supply and the amount of
electricity that can be generated from this quantity of water. In addition to the lack of fresh
water that suitable for the everyday using because the high ratio of salts in the water that
arrive to some cities through Tigris& Euphrates rivers, the problem that the other will be
faced with the continuous reduction in the arrived quantity of water to Iraq, and the
increasing in pollution levels of these rivers in the future. Where the expected pollution
levels will cross over the permition level at which the processing of water become more
difficult that the traditional water station can reach it.
Hydro Power 117
Figure 14. The map of the region of study
static (at no flow ) head loss = 80 ft dynamic(at design flow) head loss =100 ft
Q D Po/p EPM D Po/p EPM
1000 30 28.8 20736 28 36 25920
2000 39 57.6 41472 37 72 51840
3000 45 86.4 62208 43 107 77760
4000 50 115.2 82944 48 144 103680
5000 55 144 103680 52 180 129600
6000 59 172.8 124416 56 216 155520
7000 62 201.6 145152 59 252 181440
8000 65 230.4 165888 62 288 207360
9000 68 259.2 186624 65 324 233280
10000 71 288 207360 68 360 259200
Head = 400ft , Distance = 466 mile, Sys. Efficiency =50%, Q = flow rate(in gpm), D = pipe line diameter(in inch), Po/p =
power output(in KW), EPM = Energy per month(in KWH)
Table 9. Shows the Relation Between The Q (flow rate) and the o/p Power and Pipeline Diameter and
The Other Parameters are Constant.
Energy Conservation 118
From the results shown in the above tables we see that. The difference in elevation(head)
between Basra city and Hadeetha dam is 400 ft and the distance is 466 mile approximately.
To supply the city by 1000 gpm we need a pipeline with 28 inch diameter or more, and to
supply the city by 10000 gpm the pipeline of 68 inch diameter or more can be used. These
pipeline can produce a hydroelectric power from 36 KW to 360 KW which can save an
energy from 25920 KWH to 259200 KWH per month, in addition to the power saving,
through the way of supplying water with high pressure by using a pipeline, which will
consumed in the case of lifting that quantities of water from the river ( low lift ) at the
destination point to the water station or for any other using of water.
The difference in elevation(head) between Basra city and Diala (Hemrin) dam is 290 ft and the
distance is 341 mile approximately. To supply the city by 1000 gpm we need a pipeline with 28
inch diameter or more, and to supply the city by 10000 gpm the pipeline of 68 inch diameter or
more can be used. These pipelines can produce a hydroelectric power from 26.1 KW to 261
KW , which can save an energy from 18792 KWH to 187920 KWH per month in.
The difference in elevation(head) between Basra city and Abasia dam is 70 ft and the
distance is 260 mile approximately. To supply the city by 1000 gpm we need a pipeline with
36 inch diameter or more, and to supply the city by 10000 gpm the pipeline of 86 inch
diameter or more can be used. These pipelines can produce a hydroelectric power from 6.3
KW to 63 KW , which can save an energy from 4536 KWH to 45360 KWH per month
Figure (15) below shows the relations between the flow rate in gpm with pipeline diameter in
inch that represent the quantity of water supplied to the Basra city from the dams (Hadeetha,
Diala, Hindia, Abasia). The one who see this relations utilize that the graph of Hadeetha dam
and Diala is complying in spite of the difference in the dams head, because the difference in
the distances, where long distance causes high friction loss ,so that to decrease this friction loss
the pipeline diameter must be large, and the same thing shown for Abasia and Hindia dams.
Figure 15. The Relation Between Flow Rate (Q) in gpm and Pipeline Diameter in inch For Supplying
Water to Basra City from Dams
Hydro Power 119
Figure (16) below shows the relations between the flow rate in gpm that represent the
quantity of water supplied to the Basra city from the dams (Hadeetha, Diala, Hindia,
Abasia) with the hydroelectric generated power in KW. The idea behind this graph is that
the slopes of the lines increase with the increasing of head at the dams, so that the hydro
generated power from Hadeetha dam is the higher and the lower power from Abasia dam
for the same quantity of the flow rate (Q) gpm.
Figure 16. The Relation Between Flow Rate (Q) in gpm and The Hydroelectric Generated power in KW
From Supplying Water to Basra City from Dams
From all the above , if the one need to adopted this study to execute or establishing a project
of water pipelines and a micro & mini hydroelectric generators, which need to a further
studying about cost calculations and the obstacles or difficulties that may be faced him,
because this is a theoretical study and the practical project will require a solution to a
practical problems that the pipe lines intersect it , like mount , river , villages , etc.
6.2. Hydro power transportation
The use of pipeline in water transportation guarantee three type of power conservation the
first is hydroelectric generation by installing a turbine in the way of this pipeline, the second
type of power conservation when it (pipeline) may also being used instead of low lift pumping
station for the water treatment plant in this operation the power can be conserved
approximately 30% -40% of the whole total power consumed in the water treatment plants in
Babylon province when the difference in elevation between the river and the reservoir tank is
about 5-10 m (head). The using of pipeline in the supply of water directly conserved power
because it doesn't need to convert the hydropower (head & flow rate) into mechanical power
and then into electrical power that used in the low lift part of water treatment plant that need
Energy Conservation 120
to convert the electrical power into mechanical power to lift the water from the river to the
reservoir tank, because of the efficiency of conversion is always less than 100% ( turbine and
generator efficiency), this operation leads to conserve the power approximately with 50% or
more of the hydropower, which may be consider the third type of power conservation. This
type of power conservation is very clear in the water treatment plant at Bekal waterfall figure
(17) when the intake established on it, but penstock(pipeline) length is tenths meter to the
reservoir tank the length that may extended to kilometer or handered of kilometer in the other
place, which represent the low lift in the traditional water treatment plant. Also figure 18
shows the water pump used for pumping water in the water treatment station.
Figure 17. Shows the intake and the penstock (pipeline) of Bekal water treatment plant
Figure 18. Shows the high head pump station
Hydro Power 121
7. Summary
Water is one of our most valuable resources, and hydropower makes use of this
renewable treasure. Hydropower traditionally represents the energy generated by
damming a river and using turbine systems to generate electrical power. In the ancient
times waterwheels were used extensively, but it was only at the beginning of the 19th
Century with the invention of the hydro turbines that the use of hydropower got
popularized. Small-scale hydropower was the most common way of electricity generating
in the early 20
th
century. Hydropower will continue playing an important role throughout
the 21st Century, in the world of electricity supply. Hydropower development does have
some challenges besides the technical, economic and environmental advantages, which
shares with the other power generation technologies. At the beginning of the new
Millennium hydropower provided almost 20% (2600 TWh/year) of the electricity world
consumption (12900 TWh/year).
The countries have different criteria in the classification of hydro power plants, the hydro
plants may be also classified according to the Head or the vertical distance through which
the water is made to impact the turbines.
Power generation from water depends upon a combination of head and flow. Both must be
available to produce electricity. Water is diverted from a stream into a pipeline, where it is
directed downhill and through the turbine (flow). The vertical drop (head) creates pressure
at the bottom end of the pipeline. The pressurized water emerging from the end of the pipe
creates the force that drives the turbine. The turbine in turn drives the generator where
electrical power is produced. More flow or more head produces more electricity. Electrical
power output will always be slightly less than water power input due to turbine and system
inefficiencies. Water pressure or Head is created by the difference in elevation between the
water intake and the turbine.
The theoretical power (P) available from a given head of water is in exact proportion to the
head and the quantity of water available.
P= Q H e 9.81 kW
Where
P Power at the generator terminal, in kilowatts (kW)
H The gross head from the pipeline intake to the tail water in meters (m)
Q Flow in pipeline, in cubic meters per second (m
3
/s)
e The efficiency of the plant, considering head loss in the pipeline and the efficiency of
the turbine and generator, expressed by a decimal (e.g. 85% efficiency= 0.85)
9.81 is a constant and is the product of the density of water and the acceleration due to
gravity (g)
Energy Conservation 122
The penstock pipe (pipeline) transports water under pressure from the forebay tank to the
turbine, where the potential energy of the water is converted into kinetic energy in order
to rotate the turbine. The penstock is often the most expensive item in the project budget
as much as 40 percent is not uncommon in high-head installations. It is therefore
worthwhile to optimize its design in order to minimize its cost. Head loss due to friction
in the penstock pipe depends principally on the velocity of the water, the roughness of the
pipe wall and the length and diameter of the pipe. The losses decrease substantially with
increased pipe diameter. Conversely, pipe costs increase steeply with diameter. Therefore,
a compromise between cost and performance is required. Several factors should be
considered when deciding which material to use for a particular penstock: design
pressure, the roughness of the pipes interior surface, method of joining, weight and ease
of installation, accessibility to the site, design life and maintenance, weather conditions,
availability, relative cost and likelihood of structural damage. The pressure rating of the
penstock is critical because the pipe wall must be thick enough to withstand the
maximum water pressure; otherwise there will be a risk of bursting. The penstock
becomes more expensive as the pressure rating increases. The most commonly used
materials for a penstock are HDPE, uPVC and mild steel because of their suitability,
availability and affordability. Layout of the penstock pipelines depends on their material,
the nature of the terrain and environmental considerations; they are generally surface-
mounted or buried underground.
The hydrostatic pressure created from the head must be determined so that a suitable wall
thickness can be determined. This pressure is given by Equation, Pressure = p*g*H
Turbine is the main piece of equipment in the hydro power scheme that converts energy of
the falling water into the rotating shaft power. The selection of the most suitable turbine for
any particular hydro site depends mainly on two of the site characteristics head and flow
available. All turbines have a power-speed characteristic. This means they will operate most
efficiently at a particular speed, head and flow combination. Thus the desired running speed
of the generator or the devices being connected/ loading on to the turbine also influence
selection. Other important consideration is whether the turbine is expected to generate
power at part-flow conditions. The design speed of a turbine is largely determined by the
head under which it operates. Turbines can be classified as high head, medium head or low
head machines. They are also typified by the operating principle and can be either impulse
or reaction turbines.
In order to achieve the maximum (optimum) utilization of water and hydropower. The
use of pipeline in water transportation guarantee three type of power conservation the
first is hydroelectric generation by installing a turbine in the way of this pipeline, the
second type of power conservation when it (pipeline) may also being used instead of low
lift pumping station for the water treatment plant and the using of pipeline in the supply
of water directly conserved power because it doesn't need to convert the hydropower
Hydro Power 123
(head & flow rate) into mechanical power and then into electrical power which used in
the low lift part of water treatment plant that need to convert the electrical power into
mechanical power to lift the water from the river to the reservoir tank, because of the
efficiency of conversion.
Author details
Mohammed Taih Gatte and Rasim Azeez Kadhim
Ministry of Sciences and Technology, Babylon Department, Hilla, Iraq
8. References
[1] Energy Producing Systems ,Hydro Power, Energy For Missouri: Today and Tomorrow -
Educator's Guide
[2] Dilip Singh, " Micro Hydro Power Resource Assessment Handbook ", APCTT,
September 2009.
[3] Micro -Hydro Power , Practical Action, The Schumacher Centre for Technology and
Development, Bourton on Dunsmore, Rugby, Warwickshire,
www.practicalaction.org
[4] Micro-Hydropower Systems: A Buyers Guide, Her Majesty the Queen in Right of
Canada, 2004, ISBN 0-662-35880-5
[5] Jacques Chaurette p. eng. " Tutorial Centrifugal Pump Systems ", copyright 2005, Web
site: www.fluidedesign.com
[6] Md Tanbhir. Hoq, Nawshad U. A., Md. N. Islam, IbneaSina ,Md. K. Syfullah, Raiyan
Rahman, " Micro Hydro Power: Promising Solution for Off-grid Renewable Energy
Source ", International Journal of Scientific & Engineering Research, Volume 2, Issue
12, December-2011 1 ISSN 2229-5518 IJSER 2011 http://www .ijser.org
[7] Leo Lovel, Scott Craig, S. Cody Maher, Jesse Ross, Brian Van Stra, MicroHydro Turbine
A Feasibility Study
[8] Minister of Natural Resources Canada 2001 2004. " Small Hydro Project Analysis "
[9] Mohammed Taih Gatte, Rasim Azeez Kadhim, Farhan Leftah Rasheed," Using Water
Energy for Electrical Energy Conservation by Building of Micro hydroelectric
Generators on The Water Pipelines That Depend on The Difference in Elevation", IEEE
2011.
[10] Yunus A. Cengel, Michael A. Boles. " Thermodynamics an Engineering Approach ".
Fifth Edition
[11] Brian B. Yanity, "Cold Climate Problems of a MicroHydroelectric Development on
Crow Creek", The Arctic Energy Summit, Anchorage, Alaska 2007 2008.
Web sites :
http://web.archive.org/web/20070509191717/http://www.microhydropower.net/intro.html
Energy Conservation 124
http://www.bbgreeneurope.eu/vodne-turbiny/snekova-turbina
http://www.nooutage.com
Chapter 5
Earth Shelters; A Review of Energy Conservation
Properties in Earth Sheltered Housing
Akubue Jideofor Anselm
Additional information is available at the end of the chapter
http://dx.doi.org/10.5772/51873
1. Introduction
Earth sheltering is an age long traditional practice. In modern times its benefits has
prompted new definitions for its practice. With the potential thermal conservation qualities
and physical characteristics of earth as a building mass, earth shelters can now be defined as
structures built with the use of earth mass against building walls as external thermal mass,
which reduces heat loss and maintains a steady indoor air temperature throughout the
seasons. The popularity of earth sheltering was advanced mostly by research in energy
conservation in residential housing. Originally conceived as dwellings developed by the
utilization of caves within the traditional context, its evolution through technologies led to
the construction of customized earth dwellings all across the globe. These structures in the
past were built by people not schooled in any kind of formal architectural design or with
identifiable building techniques rather they depended on the cover the very structure of the
earth could provide them for purposes of shelter, warmth and security. Investigations into
the traditional earth sheltered dwellings also identified sunken earth houses with
characteristics that suggested potentials in passive building insulation which utilizes ground
thermal inertia.
In the view of some researchers on earth supported housing, building underground
provides energy savings by reducing the yearly heating and cooling loads in comparison
with known conventional structures. Not only is the temperature difference between the
exterior and interior reduced, but mostly because the building is also protected from the
direct solar radiation [1].
One significant value of earth-sheltered housing and the reason for its evaluation is its
potential energy savings when compared to conventional aboveground housing. This
potential is based on several unique physical characteristics. The first of these characteristics
is in the reduction of heat loss due to conduction through the building envelope because of
Energy Conservation 126
the high density of the earth. According to [2], in an earth sheltered building even at very
shallow depths and given normal environmental conditions, the ground temperatures
seldom reaches the outdoor air temperatures in the heat of a normal summer day. This
condition allows the conducting of less heat into the house due to the reduced temperature
differential.
In the case of colder climates, it was noticed that during winters the rate of heat loss in
bermed (earth supported) structure was less in comparison to that in on-grade structures.
This indicates through results that the floor surface temperature increased by 3 C for a 2.0m
deep bermed structure due to lower heat transfer from the building components to the
ground, thus suggesting the presence of passive heat supply from the ground even at the
extreme cold temperatures of winter [3]. This evidently contributes as a factor for energy
saving in earth shelter buildings in cold climates.
Other characteristics include the reduction of air infiltration within the dwelling which is
mainly surrounded by earth walls with very little surface area exposed to the outside air.
These characteristics have been investigated in previous studies and the analysis on each
location provides results and findings in terms of climatic effects, design styles and
residential activities of the dwellers that bring about the unique energy saving value of these
buildings.
Single unit earth sheltered houses are unique energy conservation ideas based on their earth
contact characteristics as mentioned above. In order to achieve the maximum benefits from
earth sheltered housing, its application could be examined also at an entirely community
scale rather than simply at the scale of individual houses. One of the biggest challenges to
the overall performance of earth sheltered housing would be the built conventional
surroundings. While contemporary use of earth sheltering is confined to individual homes
built on single plots of land or a small cluster of houses which will absolutely be affected by
the surrounding conventional structures around, the traditional use encompassed entire
communal design or villages that will stay within the same conditions the micro-
environment provides. This communal development option is identified to be most effective
as isolated pockets of earth sheltered houses do not really reach the scale needed for
sustainable development [4]. Earth sheltered mass-housing may thence become the general
concept for design and building with earth whereby entire communities are created,
enjoying dual land use by locating all housing underground [5]. If a single case of earth
sheltering is found to have significant advantages, these advantages can only increase in
magnitude if applied to whole communities.
2. Fundamentals of Earth sheltered housing
The values of energy conservation in earth shelters are dependent on certain principles.
These principles which form the ground rules for the design and construction of earth
sheltered dwellings have been existent since prehistoric periods. Earth sheltered homes
were primarily developed for shelter, warmth and security for the earliest human dwellers.
Earth Shelters; A Review of Energy Conservation Properties in Earth Sheltered Housing 127
Most of the recorded cases of these shelters are found extensively in areas like Asia and
Northern Africa. In one of the earliest cases in Japan was discovered the oldest human
habitation in a layer of earth about 600,000 years old in Kamitakamori, Miyagi Prefecture.
Archaeologists from the Tohoku Paleolithic Institute, Tohoku Fukushi University and other
institutes believed that the finding may be one of the oldest in the world. There are only a
few remains of human dwelling structures from the early Paleolithic period in the world, as
early humans such as the Peking-man lived in caves. Researchers believed the dwellings
were built by primitive man who appeared some 1.6 million years ago and likely reached
Japan 600,000 years ago at the latest, according to the archaeologists. The buildings could
have been used as a place to rest, a lookout for hunting, a place to store hunting tools or to
conduct religious rites.
In Tunisia, residents of Matmata were discovered to have lived in manmade caves for
centuries (Figure 1). Here rooms were carved into the soft rock to create atrium houses that
had several excavated rooms with up to 4 to 10 meter high and vaulted ceilings opening out
onto a single sunken courtyard. The original objective for going below the ground in this
case was to protect the inhabitants from the extremes of daytime North African heat and
nighttime cold, typical of this desert region.
Figure 1. Aerial view of a typical Matmata earth shelter dwelling. Image by Tore Kjeilen
However through the years, more modern earth sheltered dwellings were revealed as
studies on the earliest forms of human settlements progressed. In China, modern earth
shelters habitats were discovered with histories that dated back to before 2000 B.C. This type
of habitats were commonly called cave dwellings as they were strictly home units hewed
out of the mountains. It is believed that underground housing preceded above ground
housing in this area. Studies on these existing Chinese earth habitats presented analytical
Energy Conservation 128
data on the climatic and topographical relationships to the unique design elements utilized
to attain living comfort by the cave shelter dwellers. Such analysis as the rain, wind, sun and
seasonal weather conditions that exist in these areas where these dwellings were located
possibly necessitated the advantage of its existence in these locations [6]. Analysis on each
location also provided results and findings in terms of climatic effects, design styles and
residential activities of the dwellers. In the North-west of China, variety of these structures
evolved, ranging from the cave dwelling units to the more advanced subterranean types. In
the case of the traditional subterranean homes in China (called 'yao dong'), rooms were dug
into loose, silty soil to primarily combat the hot summers and bitterly cold winters. In the
early 20th century the provinces of Shanxi, Jiansu and Henan still had traditional dwellers
that faced with the need to preserve agricultural land and housing for their people, dug
entire cities beneath their lands. Today, it is still believed that more than 10 million Chinese
live underground, perhaps the largest number of troglodytes ever to inhabit a single region.
The Shanxi homes (Figure 2, 3 and 4) were buried at depths of up to 10 meters with their
underground homes built around courtyards. This atrium-style design offer ample sunlight
as well as surface spaces for other activities.
Research conducted in [6] also provided analytical data on climatic and topographical
relationships to the structural design styles with single unit design solution, multi unit
designs and finally urban planning initiatives on how to achieve a sunken city that exists
beneath rather than above ground level as seen in Figure 2 below. Also fascinating in
discovery included methods and techniques of ventilating the building units naturally. Such
natural ventilation techniques are viewed today as ideas that advanced the notion of passive
aeration of interiors which ultimately is a cost and energy efficient alternative to the whole
process of earth sheltered housing.
Figure 2. Aerial view of an earth shelter neighborhood in Lian Jiazhuang, Shanxi Province, North-
western China
Earth Shelters; A Review of Energy Conservation Properties in Earth Sheltered Housing 129
Figure 3. (a) Courtyard view of an Atrium type subterranean earth shelter dwelling in Lian Jiazhuang,
Shanxi Province. (b) Interior view of a typical room space. Image by Kevin Poh.
Figure 4. A typical earth shelter home layout in North-western China
With the challenges of global warming and fossil energy reduction, energy saving ideas has
become an essential element in building designs and occupation. Since energy conservation
is the practice of saving energy use without compromising occupant thermal comfort [7],
building below the ground thence presents certain fundamentals that with the aid of
(a) (b)
Energy Conservation 130
research can significantly influence energy conservation efforts in modern housing. From
reviews of the basic background of traditional earth sheltered housing, the fundamental
objectives for building below the ground and significant energy conservation principles are
listed as follows:
1. Indoor temperature enhancement based on the natural principles of annual heat storage
(PAHS) whereby the earth collects free solar heat all summer and cools passively while
heating the earth around it, and keeping warm in winter by retrieving the stored heat
from the soil in winters. This dual function presents a scenario that makes the practice
of earth sheltered housing effective in both hot and cold climates.
2. Huge temperature differential between the ground temperatures and the outdoor air
temperatures. In this case the normal ground temperature seldom reaches the outdoor
air temperatures in the heat of a normal hot day, thereby conducting less heat into the
house due to the reduced temperature difference.
3. Building protection from the direct solar radiation, thereby elimination the challenge of
direct thermal load due to heat radiation through the building envelope.
Apart from the energy values which the subsurface climate of the earth provides, the other
significant characters beneficial to earth shelters includes the major goal of recycling surface
space by relocating functions to underground, by this earth shelters liberates valuable
surface space for other functional uses and improves ground surface visual environment,
open surfaces for landscaping and thus a more greener atmosphere.
3. Modern construction techniques and design typology
The structural make up of a typical earth shelter house is made up of the supporting
members and the compacted backfills in which case strength and composition can
determine the ability to withstand overhead loads of moisture, dead and live loads, the
distribution of which depend on the compaction strength of the backfill or supports.
However in modern designs, the supports are the parts of the house that brace against the
side walls of soil and overlaying roof members that are made of backfills as in the case of
underground homes. The design method and material choice will determine the resistance
to failure of these structural members. In the traditional construction scenario where the
earth-soil is used as building material; its strength is determined by the soil stability, which
goes to improve the resistance to wind and in most cases rain erosion.
3.1. Earth shelter structural integrity
The structural make up of earth homes is mainly made up of the supporting members and
the compacted backfills. As earlier mentioned, the strength and composition of the material
used as backfill can determine the ability to withstand overhead loads. The supports are the
parts of the house that brace against the side walls of soil and overlaying roof members that
are made of backfills. The building design method and material choice will determine the
resistance to failure of these structural members. In the case where the earth-soil is used as
Earth Shelters; A Review of Energy Conservation Properties in Earth Sheltered Housing 131
building material, its strength is determined by the soil stability, which goes to improved
the resistance to wind and rain erosion. In most earth shelter construction the significant
structural areas are the soil, walls and roof area. Apart from serving as a building material,
the soil-walls of the shelter trench are regarded as the most valuable structural member of
the Earth house structure. It provides the necessary support a normal wall gives in an
ordinary house design. Nevertheless, not all soil types are efficient in use for earth sheltered
house construction. From studies it is identified that the best soils are granular, such as sand
and gravel. These soils compact well for bearing the weight of the construction materials
and are very permeable, which means they allow water to drain quickly. The poorest soils
are cohesive, like clay, which may expand when wet and has poor permeability. Soil tests,
offered through professional testing services, can determine load-bearing capability of soils
and possible settlements that may occur after construction. Study in [6] revealed certain
traditional considerations for deciding the depth, thickness of mass and curvature of the
support ceilings (vault) of the Chinese earth homes which can also be applied in modern
day construction of earth shelters (figure 5).
Figure 5. Structural consideration for a typical room space excavation in the Shanxi traditional earth
shelters
h =1 ~2, = 18.
B = B + H t g (45 - 2)
= 3.5 2 + 3 t g (45 - 18 2)
B = 1.75 + 2.19 = 3.94 m
Then S = Thickness of Earth thermal mass wall
H3 = Extent of depth clearance
Assuming B (room span) = 3.5m and H (room height) = 3m
H3 = Depth from ground surface to ceiling. This should be greater than h
The Dotted/shaded area indicates possible fault lines due to the pressure from the
overlaying earth mass
Energy Conservation 132
Varieties of techniques have been used in the past for earth shelter wall construction. The
construction materials for the walls of each type of structure will vary, depending on
characteristics of the site, climate, soils, and design. However, general guidelines show that
houses more deeply buried require stronger, more durable structural walls. Walls must
provide a good surface for waterproofing and insulation to withstand the pressure and
moisture of the surrounding ground. When soil is wet or frozen, the pressure on the walls
and floors increases as pressure also increases with depth.
For the traditional earth supported homes built in the Chinese and Arid (dessert) climatic
regions, there usually is no use for supporting walls as the naturally compressed soil
structure already serves the function. However through recent research on improving the
state of earth homes for most other climatic regions, the walls of Earth homes can be made
of various materials ranging from Compressed Earth bricks to Concrete, while providing
cavities and drainage patterns to aid damp proofing. In most earth home designs, the roof is
usually the most challenging part of the entire structure. With recent ideas in ecology, the
roof of earth shelters assume interesting landscaping functions. Especially for earth
supported shelters which already posses the natural materials of earthen walls and
members, the roof can also be finished to assume a natural finish too. Since the basic idea of
this study is to discover techniques to achieve high performance as possible, the basic
structural form for constructing the earth shelter roof is as follows:
1. A frame strong enough to support the dead load brought by the soil overlay, rain, snow
and ice loads where applicable.
2. A solid deck built over the frame and a waterproof membrane installed on the deck
prior to final earth cover.
3. Treated soil backfill placed on the membrane (as the roof layer) and covered with a fine
thick layer of soil. The roof will either grow a vegetation of its own or become a life
garden depending on the appropriate type of maintenance.
Reinforced concrete is the most commonly used structural material in earth shelter
construction. Products like Grancrete and Hycrete are becoming more readily available.
They claim to be environmentally friendly and either reduce or eliminate the need for
additional waterproofing. However, these are new products and have not been extensively
used in earth shelter construction.
Some other unconventional approaches are also utilized in earth shelter construction. These
techniques utilize recycled material of various forms and applications. One of such
approaches is referred to as an Earth ship (figure 6). These houses are built to be self-
contained and independent; their design allows occupants to grow food inside and to
maintain their own water and solar electrical systems [8]. Some builders believe they have
proven the design's ability to tap into the constant temperature of the earth and store
additional energy from the sun in winter. These Earth ships carry out their environmentally
conscious theme by employing unusual building materials in the form of recycled
automobile tires filled with compacted earth for thermal mass and structure. While the tires
form the major structural frames for the building, aluminum or tin cans are used for filling
Earth Shelters; A Review of Energy Conservation Properties in Earth Sheltered Housing 133
minor walls that are not load-bearing. Foam insulation can be applied to exposed exterior or
interior walls and covered with stucco. Interior walls are also dry-walled giving it a
conventional look.
Figure 6. An Earth Ship design, using recycled materials
3.2. Earth shelter construction typology
Earth sheltered houses are often constructed with energy conservation and savings in mind.
Though techniques of earth shelter construction have not yet become common knowledge,
study into the most efficient application of the earth shelter principles reveals classifications
of the major typologies that are utilized in the construction of earth houses. These major
construction concepts are the Bermed or banked with earth type and the Envelope or True
underground type. The energy conservation values of these typologies also vary depending
on climate and physical challenges indigenous to each typology (table 1).
a. Bermed earth shelter: In this type of construction, earth is piled up against exterior
walls and heaped to incline downwards away from the house. The roof may, or may
not be, fully earth covered, and windows/openings may occur on one or more sides of
the shelter. Due to the building being above ground, fewer moisture problems are
Energy Conservation 134
associated with earth berming in comparison to the fully underground construction.
Other variations of bermed construction are the elevational and in-hill construction
(figure 7). This type of construction is particularly appropriate for colder climates. With
regards to energy efficiency in colder climates, all the living spaces may be arranged on
the side of the house facing the equator. This provides maximum solar radiation to the
most frequently used spaces like bedrooms, living rooms, and kitchen spaces [9].
Rooms that do not require natural daylight and extensive heating such as the bathroom,
storage and utility rooms are typically located on the opposite in-hill side of the shelter.
The compact configuration of this construction provides it with a greater ratio of earth
cover to exposed wall thereby improving its energy performance benefits through the
earth-contact principles. However the case for both climates, the three major
determinants for the building orientation remains the sun, wind and outside views.
Proper orientation with respect to solar path and wind is significant for energy savings.
Figure 7. (a) Elevational (beremed) and in-hill designs, (b) Atrium (bermed) design
b. Envelope or True underground earth shelter: In the true underground construction,
the house is built completely below ground on a flat site, with the major living spaces
surrounding a central outdoor courtyard or atrium. The windows and glass doors that
are on the exposed walls facing the atrium provide light, solar heat, outside views, and
access via a stairway from the ground level. The atrium effect offers the potential for
natural ventilation. In the view of some researchers, this concept reduces the energy
conservation properties in colder climates mostly due to the reduced solar exposure
Earth Shelters; A Review of Energy Conservation Properties in Earth Sheltered Housing 135
within the courtyard or atrium opening [9]. However recent studies in the area of soil
temperature analysis with respect to energy conservation in earth shelters, provides
information on the prospect of efficient underground earth shelter design. Such studies
as in [10], provides mathematical method for predicting the long-term annual pattern of
soil temperature variations as a function of depth and time for different soils and soil
properties that are stable over time and depth. The likes of these studies were utilized
by John Hait's [11] in his book on Passive Annual Heat Storage (PAHS) to advance the
ideas of earth shelter housing. With the development of modern passive solar building
design, during the 1970s and 1980s a number of techniques are developed to enabled
thermally and moisture-protected soil to be used as an effective seasonal storage
medium for space heating, with direct conduction as the heat return method. Other
variations of the true underground typology are the Atrium/courtyard concept and the
Penetrational type where earth covers the entire house, except where it is retained for
windows and doors for cross-ventilation opportunities and access to natural light from
more than one side of the house (figure 8).
Figure 8. Underground earth shelter design
One of the most significant earth sheltered buildings in modern times is the Aloni House
(figure 9). It was built in Antiparos Island in Greece and won the Greek Piranesi Award in
2009. The building epitomizes all that a modern time earth shelter represents. It combines all
the design types mentioned above within a unique terrain. It also provided courtyard spaces
Energy Conservation 136
with its landscape appearing to drift naturally into the courtyard thereby allowing for free
solar penetration to the desired areas.
Factor Earth shelter building type
Bermed Envelope/true underground
Passive solar potential Excellent Less effective
Thermal stability Less effective Excellent
Natural lighting potential Effective Less effective
Wind protection Less effective Excellent
Noise protection Less effective Excellent
Visual convenience Excellent (one directional view)
Poor (allows only open sky
view)
Appropriate Climate Effective for temperate Most effective for tropical
Structural cost
Modern
design
Vernacular
design
Modern design
Vernacular
design
Intermediate Less expensive Most expensive
Least
expensive
Table 1. Comparing efficiency values of the earth shelter building typology
Figure 9. Images of the Aloni House. (a) view from the hill top, (b) view from the top of the house, (c)
opening leading to the courtyard, (d) the central courtyard, (e) interior view of the living room, (f)
interior view from the kitchen. (Images by Julia Klimi)
Earth Shelters; A Review of Energy Conservation Properties in Earth Sheltered Housing 137
4. Evaluation of energy conservation principles in earth shelter schemes
The most significant value of earth shelters and the basis for the exploitation of earth in
energy saving building initiatives is its energy preservation potential. This is based on
several unique physical characteristics of earth. As stated earlier, the dependability of earth
in energy conservation designs is related to the natural principles of annual heat storage;
huge temperature differential between the ground temperatures and the outdoor air
temperatures and the insulation properties from direct solar radiation. In the cold climates,
the significant property is the reduction of heat loss due to conduction through the building
envelope. The amount of heat lost in this manner is a function of the thermal transmission
coefficient (R-factor) of the envelope and the temperature difference between the inside of
the envelope and the outside. While the R-factor for earth is substantially lower than that of
other insulating materials, the large amount of earth inherent in earth sheltering can provide
an overall R-factor comparable with more highly insulated structures [12].
According to investigations in [12], the temperature differential for conventional above
ground structures is the difference between the outside air temperature and the interior
temperature maintained for the comfort of its inhabitant. Under extreme conditions, this
differential can be as much as 32C. However, since the daily and seasonal fluctuations of
temperature below the surface of the ground never equals that of the air above, therefore the
deeper the temperature is taken, the less severe will be the variation. This reduced
temperature differential results from the thermal storage capabilities of the soil which
moderate extremes of temperature and create seasonal intervals, wherein energy from one
season is transferred to the next season as in the principle of PAHS.
4.1. Solar radiation and energy conservation in earth sheltered houses
It is common knowledge that the sun is one of the most significant determinants in energy
efficient building design. The radiant energy from the sun can be used as both active and
passive heat generators for a building. Generally in colder climates, the active solar receptor
system is oriented directly to the south, whereas all passive solar collection methods are
based on trapping the radiant energy of the sun which enters through the openings on the
building envelope. In the case of earth sheltered houses, the best site orientation (in cold
climates) is the south-side orientation which maximizes the presence of all of the window
openings whereas the remaining sides of the building are completely earth covered. The use
of passive solar collection in combination with other energy conservation values is a very
desirable energy efficient concept in buildings since it does not involve the capital expense
that an active solar collector does. Conversely, it is important to note that, while solar
radiation is desirable in the heating season of cold climates, they are not as efficient in the
cooling season of hotter climates. The effect of wind on the orientation of an earth sheltered
structure is a serious energy consideration [13]. Since direct exposure to cold winter winds
increases heat loss due to infiltration which consequently creates a wind chill effect, it is
desirable to protect a building as much as possible from this exposure. In the north
hemisphere the prevailing winter winds are from the northwest. Minimizing window and
Energy Conservation 138
door openings on the north and west sides of the house in this region will enhance energy
performance.
4.2. Effects of seasonal thermal storage systems on energy conservation in earth
sheltered houses
A seasonal storage system can broadly be defined as one which stores energy in one season
and delivers that energy in another season. Naturally for seasonal storage systems that
function as solar thermal collectors, this means that energy is collected in periods of high
radiation as is the case in summer seasons and delivered in winter seasons during periods of
low radiation. However to further improve the efficiency of any of the seasonal thermal
storage systems, very effective above-ground insulation or super insulation of the building
structure is required to minimize heat-loss from the building, thereby improving the
amount of heat that needs to be stored and used for space heating.
There are three major types of seasonal (annualized) storage systems that are classified as
effective or beneficial to earth shelter buildings. These are:
4.2.1. Low temperature systems:
This system utilizes the earth (soil) adjoining the building as a low-temperature seasonal
heat store, thereby reaching temperatures similar to average annual air temperature while
drawing upon the already stored heat for space heating. These systems can also be seen as
an extension to the building design itself as the design involves some simple but significant
differences when compared to conventional above ground buildings.
4.2.2. Warm temperature inter-seasonal heat system:
This also uses soil to store heat, but utilizes active solar collection mechanisms in summer to
heat up thermal banks (earth mass) in advance of the heating season. Warm temperature
heat stores are generated from low-temperature stores in that solar collectors are used to
capture surplus heat in summer and actively raise the temperature of large mass of soil so
that heat extraction is made cheaper in winter.
4.2.3. Passive annual heat storage system (PAHS):
With the development of modern passive solar building design, during the 1970s and 1980s
a number of techniques were developed that enabled thermally induced and moisture-
protected soil to be used as an effective seasonal storage medium for space heating, with
direct conduction as the heat return method. The concept of Passive Annual Heat Storage
(PAHS) is such that solar heat is directly captured by the structure's spaces and surfaces in
summer and then passively transferred through its floors, walls and roof into adjoining
thermally-buffered soil by conduction. It is then passively returned to the building's spaces
through conduction and radiation as those spaces cool in winter. This idea was originally
Earth Shelters; A Review of Energy Conservation Properties in Earth Sheltered Housing 139
introduced by John Hait [11]. It includes extensive use of natural heat flow methods, and the
arrangement of building materials to direct this passive energy from the earth to the
building, all without using equipment. PAHS is believed to be one of the most significant
ideas for energy conservation in earth sheltered buildings.
Concept of passive annual heat storage system (PAHS):
Globally, the earth receives electromagnetic radiation from the sun which is typically
defined as short-wave radiation and emits it at longer wavelengths known typically as long-
wave radiation. Figure 10 below shows an analysis of the earths shortwave and long-wave
energy fluxes produced with details from [14]. This absorption and re-emission of radiation
at the earths surface level which forms a part of the heat transfer in the earths planetary
domain yields the idea for the principle of PAHS. When averaged globally and annually,
about 49% of the solar radiation striking the earth and its atmosphere is absorbed at the
surface (meaning that the atmosphere absorbs 20% of the incoming radiation and the
remaining 31% is reflected back to space). This absorbed 49% of the solar radiation presents
a premise for energy efficiency in building design. The concept of earth shelter design
focuses fundamentally on the utilization of the absorbed/retained heat from this annual
absorption and re-emission of radiation for indoor thermal environment control.
Figure 10. Earths energy budget diagram showing the short-wave (a) and long-wave (b) energy fluxes
4.3. Analysis of soil thermal performance in earth shelter designs
The thermal property of an earth-shelter soil is an essential factor in determining its
performance against other conventional above-grond houses. Due to the relatively stable
Energy Conservation 140
temperature of the soil, the earth shelter house in summer loses heat to the cool earth rather
than gaining heat from the surrounding air, and in winter the relatively warm soil offers a
much better temperature environment than the subzero air temperatures. This concept is
clearly confirmed by examination of the daily and yearly soil temperature fluctuations at
various depths. Daily fluctuations are virtually eliminated even at a depth of 20 cm of soil.
At greater depths, soil temperature responds only to seasonal changes, and the temperature
change occurs after considerable delay [15]. A reasonable level of soil study is necessary in
order to facilitate the comparison of the energy needed for construction (soil excavation,
dewatering and concrete works) with the energy to be saved in the long run, conditions
related to the insulation efficiency of the soil [16]. However the expected efficiency varies
with the soil type and its water content which in some cases may have a marked effect on
the thermal properties of the soil. The figure below (Figure 11) presents a typical
relationship between the annual air temperatures and corresponding temperature
fluctuation below the ground surface.
Figure 11. Annual temperature fluctuations in Riyadh from below zero to 48 C and expected
temperature fluctuation at 3.0m below ground level between 14C and 24C. (Data taken from [16])
In earth shelter houses, the overlaying thick earthen layer around much of the building
effectively eliminates possibilities of infiltration through the building skin (as is the case in
conventional above-ground houses). This can contribute significantly in reducing energy
loss due to infiltration, except only through the exposed portions of the structure. Apart
from the reduction of infiltration, studies identified that the application of thermal coupling
of the earth-soil to the building wall places significant values to the thermal conditions of
the earth shelter environment in winters. This process allows for improved thermal storage
through the soil into the building walls. Since majority of modern earth shelters are built
with concrete which possesses a large thermal storage capacity which can absorb the excess
energy from the earth-soil, this absorbed heat is naturally released back into the building
whenever the indoor air temperature is below that of the thermal mass. This thermal
Earth Shelters; A Review of Energy Conservation Properties in Earth Sheltered Housing 141
absorption and releasing process can provide essential heat energy required in the house for
days without mechanical heating. The effect of this process is presented below (figure 12) in
a thermal investigation study of a berm-type earth sheltered house in Missouri (US)
covering a 4 day assessment period under a 6-hourly measurement interval [12].
Figure 12. Temperature stability graph of an earth sheltered house in Missouri (Data taken from [12])
Determining the thermal performance of the soil for earth shelter construction involves
assessing the long-term subsurface environment and above-ground temperature data.
Consequently, this requires accurate environmental information on the boundary
conditions, one of which is the temperature of the surrounding soil. For instance, in the case
of a single basement study, a change in the mean annual ground temperature from 10C to 6
C caused a 36% increase in heat loss [17]. Therefore, accurate data regarding diurnal and
annual variation of soil temperatures at various depths is necessary to accurately predict the
thermal performance of earth sheltered structures.
Study shows that actual data on soil temperatures is not usually abundant. However
research has facilitated the evaluation of the underground climate in order to assess the
suitability of earth sheltered structures. Algorithms for this calculation of the soil
temperatures at various depths have already been developed based on existing field
measurements in different regions of the world and by this, the annual pattern of soil
temperatures at any depth can be accurately considered as a sine wave about the annual
average of the ground surface temperature. Accordingly, a mathematical method was
developed to predict the long-term annual pattern of soil temperature variations as a
function of depth and time for different soils and soil properties that are stable over time
and depth [10]. This method is sufficiently accurate in the case certain thermal and physical
characteristics are accurately estimated. The equation for estimating subsurface
temperatures as a function of depth and day of the year is as follows (with the unit of cosine
expressed in rad):
Energy Conservation 142
( , ) 0
2 365
e / 365 cos
365 2
x
x t m s
x
t t
t
t o
to
( | |
| |
( |
` |
|
( \ .
\ .
=
)
T T A (1)
Where:
T
(x,t)
= subsurface temperature at depth x(m) on day t of the year (C),
T
m
= mean annual ground temperature (equal to steady state) (C), as the annual
temperature amplitude at the surface (x = 0) (C),
x = subsurface depth (m),
t = the time of the year (days) where January 1 = 1 (numbers),
t
0
= constant, corresponding to the day of minimum surface temperature (days),
= the thermal diffusivity of the soil (m
2
/day)
Through this equation, the resulting temperature profile at different depths can now be
graphed and compared with the annual average air temperatures. Following the
evaluation of the subsurface climate, the calculated soil temperatures can then be used to
calculate the heat flux through the building surfaces. The energy efficiency of a wall in
contact with the earth at varying depths can thus be investigated for local climatic
conditions. This can be done by simulating the heat transfer through a subsurface wall at
varying depths using a computer program, and comparing the results with an above-
ground wall using the same method. This procedure is a typical preliminary assessment
method with minimal input required. The expected results from the simulations provides
preliminary insight into the magnitude of reduction of heat flow that the building soil
climate can provide in comparison to the above-grade climate and the analysis also
provides a faster approach for determining the optimum depth placement for an earth
sheltered building.
Although this theory seems rightly beneficial to the energy conservation concepts in earth
shelter house construction, it is also right to consider other detrimental factors like the soil's
heat and cooling losses due to normal thermal transmittance factors. Earth shelters are
subjected to heat and cooling losses partly via the soil to the external air, via the soil to the
groundwater below or directly to the groundwater. The quantity of loss is calculable in this
case and the equation is generated in [18] as follows:
( )
i
i
v vOT
v vGW
QT Atotal W
RAL RGW
( = +
(2)
Where:
00I = mean outside temperature
0 to -5C (0e + 15K)
R0I = Ri + RzA + RzB + Rc = equivalent resistance to thermal transmission room-outside air.
RzA = equivalent resistance of the soil to thermal conductivity.
RzB = resistance of building component to thermal conductivity.
Earth Shelters; A Review of Energy Conservation Properties in Earth Sheltered Housing 143
RuW= Ri + RzB + Rzs = equivalent resistance to thermal transmission room-groundwater.
Rzs = T/zs = thermal conductivity resistance of soil to groundwater.
D = depth of groundwater
zs = thermal conductivity coefficient of soil
1.2 W/mK
0uW= groundwater temperature = 10C.
4.4. Energy conservation values in earth shelter design
Earth is a great moderator of temperature change. When warmed up, it can stay
warm a long time without losing much of its heat [9]. Earth does not react as fast to
temperature change as air does. This means that for instance if air surface temperatures
ranges from -15C to 35C through the year (winter through summer), then about
3 meters below, the temperature of the earth will vary only between 10C to 15C.
This short range in difference explains the ability of earth to maintain stable temperatures
throughout the year. This is a significant energy conservation tendency in the case of
reducing the load on home heating and air-conditioning systems. With regards to total
operating cost (excluding estimates from heat-recovery systems), energy savings of up to
60% to 70% may be realized in residential scale structures within mid-temperate zones.
Instances of this were presented in [19] from the energy cost studies undertaken in [20]. In
this study, a conventional 135 sq m (9m x 15m) single level residence with a hypothetical
subsurface structure of the same dimension was compared. With the use of climate data
and energy rates of Denver metropolis in Colorado, the study establish that the
underground house provides a 72% energy savings over the surface dwelling (Table 2, 3
and 4).
Measured unit Conventional surface house Earth shelter house
Heat loss in winter (B.T.U. per hour) 39,927 12,720
Heat gain in summer (B.T.U. per
hour)
44,650 0
Table 2. Evaluation of rates of heat loss and gain in a typical above ground house and an earth
sheltered house [20]
Measured unit Conventional surface house Earth shelter house
Winter:
Gas (m
3
)
Oil (gal.)
electricity (kwh)
2,656.9 m
3
($65.80)
710 ($129.90)
23,157 ($428.80)
871.5 m
3
($27.60)
233 ($42.60)
7,596 ($191.10)
Summer
Electricity (kwh)
3,962 ($98.40)
0
Table 3. Evaluation of annual energy consumption cost in a typical above ground house and an earth
sheltered house [20]
Energy Conservation 144
Building type Gas Oil Electricity
Above ground design (AGD) ($395) ($459) ($758)
Earth sheltered design (ESD) ($120) ($135) ($283)
Cost conservation comparison
between ESD and AGD
30% 29% 37%
Table 4. Evaluation of annual cost of environmental control requirements in a typical above ground
house and an earth sheltered house [20]
5. Soil suitability analysis for earth sheltered building construction
As already discussed earlier, not all soil types are efficient in use for earth sheltered building
construction. The choice of construction site is mainly determined by the soil type available in
a given geographical area for issues of safety against landslides and other moisture originated
hazards. Some types of soil are more suitable than others in the construction of sub-grade
buildings. The strength of the soil must be determined for the proposed depth of building
below ground level. Though may be desirous, excavations in a very strong soil may be difficult
and in the case of rocky ground, may prove impossible. On the other hand, in very weak soils
the excavations are easy. In the first two cases, the capital cost and the energy expenditures
involved in construction need careful examination [21]. For the third case, however, the
excavation may be difficult because high lateral earth pressure requires construction of heavy
walls (retaining walls), preferably made of reinforced concrete, which implies increased capital
costs and energy consumption. In modern earth sheltered home construction, compaction and
permeability values are the most essential standards considered in the backfill process when
building a berm or elevational type construction. This is mostly due to the dangers of soil
drainage. It has been noted earlier that soil-water content has distinctive effect on the thermal
properties of the soil hence may affect the overall energy performance of earth-homes.
Choosing a site where the water will naturally drain away from the building is the best way to
avoid water pressure against underground walls. In order to improve the energy performance
of the earth-soil in temperate, humid or arid tropical scenarios, drainage systems must be
designed to draw water away from the structure to reduce the frequency and length of time
the water remains in contact with the building's exterior. Survey has identified that ideal sites
are those of hilly or mountainous terrain. The partially buried (bermed-elevational) earth-
sheltered home is identified as most suitable for maximizing passive-solar heating in cold
climates, however since water tends to drain down the hill toward the building and off the
roof toward the back of the home, it is advisable to build in highly water-permeable soils and
to install water drainage systems around the perimeter of the buried walls. Hydrology
discusses infiltration as the rate at which water passes into the soil. This is also affected by the
ratio of macro to micro-pores of the soil in question. The more macro-pores a soil has the easier
it is for water to soak into it and drain away. Soils with coarse particles like sand or gravel or
nutty or block soil structures have a high proportion of macro-pores and as a result have high
infiltration rates. Soils such as clays have a high proportion of micro-pores and therefore have
low infiltration rates. Figure 14 below illustrates different infiltration rates based on soil
structure and texture [22].
Earth Shelters; A Review of Energy Conservation Properties in Earth Sheltered Housing 145
Through the analysis below, it could be said that a good earth home design site with natural
drainage also requires permeable soils. The most permeable soils as identified above are the
granular type which consists of a fair amount of sand or gravel while soils with high clay
content are less permeable as they expand and contract as moisture levels fluctuate.
Nonetheless, it is advisable to perform percolation tests on the construction site's soil to
determine the earth shelter soil permeability before construction.
Figure 13. Infiltration curves for different soil textures
6. Thermal Integrity Analysis of earth sheltered houses
Thermal integrity factor (TIF) is a combined system for evaluating and comparing the
energy performance values of building types. It is expressed in units which allow for direct
comparison among such criterion as heating, ventilating, and air conditioning systems as
well as the effect of various climatic conditions on different housing types. The standard
unit for measuring thermal integrity values is Btu/ft
2
per degree day of the provided space
condition. A TIF of 7.5 Btu/ft
2
per heating degree day is considered as representative of a
baseline-factor for moderately insulated houses [23], while values in the ranges of 0.6 to 1.1
Btu/ft
2
per heating degree day are predicted for super-insulated houses [24]. Early indication
of the performance of earth sheltered buildings against the conventional above-ground ones
were recorded as far back as the late 1970s and 80s. Measurements were conducted on
existing earth sheltered houses in some US cities. In one of the houses located in South
Dakota which was monitored during 1978 and 1979, it consumed about 28,000 Btu/ft
2
for
8144 heating degree days, which yields a TIF of 3.5 Btu/ft
2
per heating degree day. The
report on this house went on to note that typical above-ground framed homes in the same
location generally required about 10 to 12 Btu/ft
2
per heating-degree day. This displays a
Energy Conservation 146
70% difference in the TIF of these two homes in the same location. Figure 13 below shows
the comparative energy consumption for the above-ground and earth sheltered homes. In
some other cases, earth sheltered houses display TIFs of 0 (zero) Btu/ft
2
per heating degree
day. Below (table 5) are the results of the TIFs for five different buildings in Minnesota all of
which recorded TIFs of less than 4.0 [25].
Figure 14. Comparison of monthly total energy usage in conventional above-ground and earth
sheltered homes (taken from [12])
House
June
1980
July
1980
Aug.
1980
Sept.
1980
Oct.
1980
Nov.
1980
Dec.
1980
Jan.
1981
Feb.
1981
Burnsville nil nil nil 0.65 0.84 nil nil nil 2.03
Camden 0 0 0 0 0.89 1.20 2.65 1.92 nil
Seward 0 0 0 0 0 2.14 3.60 2.53 3.19
Wild River 0 0 0 0 0.19 2.05 1.08 0.91 1.27
Willmar nil nil nil 2.28 2.34 1.23 2.72 2.01 nil
'nil' = No data taken.
Table 5. Monthly thermal integrity factor for five Minnesota earth-sheltered residences
7. Conclusion
In this study, the following factors were analyzed in the hope of throwing light into the
common questions that arise in the discourse of earth sheltered housing:
a. Energy conservation elements for earth shelter housing,
b. Thermal integrity values,
c. Techniques for maximizing the thermal loads necessary for comfort conditions in
passively heated or passively cooled earth shelters,
Earth Shelters; A Review of Energy Conservation Properties in Earth Sheltered Housing 147
d. Soil suitability, depth of placement and design techniques that optimizes structural
integrity in earth sheltered house construction.
This study also presented some of the valuable analysis and results in earth shelter building
evaluations as premise for assessing the potentials of passively heated earth sheltered
houses. This is achieved through a review of previous performance assessments of
monitored conditions in existing earth sheltered buildings. Through this review, thermal
integrity factors (TIF) of existing earth sheltered homes were identified, which when
compared with other housing types, perform significantly better than conventional above-
ground dwellings. It also looked at both summer and winter impacts of earth shelter house
types utilizing the passive approach under the different climate conditions. This study
identified that the thermal integrity value of passively heated earth sheltered house is
comparable with other energy-efficient approaches such as super-insulated and passive
solar constructions which are much better in energy conservation performance than the
conventional above-ground constructions. It further presents the criteria for identifying the
appropriate soil type (sub-grade materials) needed in building earth sheltered houses with
passive thermal approach. These are categorized under thermal inertia properties, bearing
capacity and drainage properties. Based on the available information to date, it can be said
that earth sheltered houses maintain heating energy consumption that is lesser by up to
75%. This claim appears to be substantiated as earth sheltered house compared to
conventional above-ground house presents a lesser calculated or monitored TIF.
Having looked through the benefits and potentials of earth and the overall understanding of
its potential for energy conservation through earth-sheltered construction, it is hoped that
this review contributes to the information available so far on means of assessing the
performance of earth shelters and associated thermal properties that affects it. It is then
possible for designers and planners in different regions to have access to a simple
framework for assessing its efficiency at the initial planning stages. The resulting outputs
can then be used for the heat transfer and energy conservation analysis within the building
units. Results from this analysis will provides insight into the degree of passive heating and
cooling or reduction in heat flow that the soil climate can provide as compared to the
surface climate as well as suggesting parameters for depth placement of earth shelter
buildings for more efficient results.
Author details
Akubue Jideofor Anselm
Architecture Department, University of Nigeria, Nigeria
8. References
[1] Carpenter P, (1994) Sod It: An Introduction to Earth Sheltered Development in England
and Wales, Coventry University, Coventry,.
[2] Carmody J, Sterling R, (1984) Design considerations for underground buildings,
Underground Space 8: 352-362.
Energy Conservation 148
[3] Kumar R, Sachdevab S, Kaushik S.C, (2007) Dynamic earth-contact building: A
sustainable low-energy technology, Building and Environment 42: 2450-2460.
[4] Dodd J, (1993) Earth sheltered settlements, a sustainable alternative, in: Proceedings of
the Earth Shelter Conference, Coventry University 3: 26-36.
[5] Moreland F.L, (1975) An alternative to suburbia, in: Proceedings of the Conference on
Alternatives in Energy Conservation: The Use of Earth-covered Buildings, National
Science Foundation, Fort Worth, TX,.
[6] Golany G. S, (1983) Earth Sheltered Habitat (History, Architecture and Urban Design),
Van Nostrand Reinhold Company Inc., New York.
[7] Rahman M.M, Rasul M.G, Khan M.M.K, (2010) Energy conservation measures in an
institutional building in sub-tropical climate in Australia. Applied Energy 87: 2994-3004
[8] Reynolds M, (1991) Earth-ship Systems and Components, Solar Survival Press
[9] Wells M. B, (1975) To Build without Destroying the Earth. Alternatives in Energy
Conservation: The Use of Earth Covered Buildings. Washington, D.C. U.S. Government
Printing office. Pp. 211-232
[10] Labs K, (1979) Underground building climate, Solar Age 4: 10 44-50.
[11] Hait J, (1983) Passive Annual Heat Storage: Improving the Design of Earth Shelters,
Rocky Mountain Research Center
[12] Wendt R. L, (1982) Earth-Sheltered Housing: An Evaluation of Energy-Conservation
Potential. U.S. Department Of Energy, Oak Ridge Operations, TN. pp. 8-18,
[13] Minnesota University (1979). The Underground Space Center, Earth Sheltered Housing
Design. Minneapolis, Minnesota: Van Nostrand Reinhold Company. pp. 20
[14] Bonan G, (2002) Ecological Climatology: Concepts and Applications, Cambridge Press,
United Kingdom
[15] US Department of Housing and Urban Development, (1980). Earth Sheltered Housing
Code, Zoning, and Financing Issues
[16] Khair-El-Din A. M, (1991) Earth Sheltered Housing: An Approach to Energy
Conservation in Hot Arid Areas Architecture and Planning Riyadh. 3:3-18
[17] Mitalas G.P, (1982) Basement Heat Loss Studies, DBR/NRC, Ottawa.
[18] Klaus D, (2003) Advanced Building Systems: A Technical Guide for Architects and
Engineers, Published for Architecture Basel, Boston, Berlin. pp. 50.
[19] Labs K, (1975) The Architectural Use of Underground Space: Issues and Application.
Masters Thesis/Washington University, May, Mechanicsville PA. pp. 121
[20] Harrison L, (1975) Is it time to go Underground? The Navy Civil Engineer, Fall. pp. 28-29
[21] Henna A. M, (1980) Building Underground Alternatives. Miami published research for
the Energy Conservation Conference, Florida.
[22] McLaren R. G, Cameron K. C, (1990) Soil science. An introduction to Properties and
Management of New Zealand Soils. Oxford university press, Auckland.
[23] Lewis D, Fuller W, (1979). Solar Age, p. 31
[24] Shurcliff W. A, (1980). Super-insulated Houses and Double-Envelope Houses, A
Preliminary Survey of Principles and Practice, 2nd Ed., Cambridge, Mass. p. 6.05.
[25] Goldberg L. F, Lane C. A, (1981). A Preliminary Experimental Energy Performance
Assessment of Five Houses in the MHFA Earth-sheltered Housing Demonstration
Program, University of Minnesota, Minneapolis. pp. 10.
Chapter 6
Low Energy-Consumption Industrial Production
of Ultra-Fine Spherical Cobalt Powders
Chong-Hu Wu
Additional information is available at the end of the chapter
http://dx.doi.org/10.5772/52113
1. Introduction
Cobalt powders have been used extensively in cemented carbides, high-temperature alloys,
PCD and PCBN, and magnetic materials, etc., due to its excellent physical, chemical, and
mechanical properties. The fabrication and final properties of the above materials are
strongly affected by the quality (purity, phase, size, shape, dispersity, fluidity, etc.) of Co
powders. In order to fabricate a homogeneous and densified microstructure without pores,
Co-pool, Co-poor and Co-free zones, etc., ultra-fine spherical Co powders have been desired
with the development of ultra-fine and even nano grain materials. However, it is very
difficult to industrial fabricate ultra-fine spherical Co powders with good quality by the
conventional decomposition and hydrogen-reduction technology. In this paper, a new low
energy-consumption industrial production technology-a continuously dynamic-controlled
combustion synthesis (CDCCS) technology has been proposed about investigating how to
obtain ultra-fine spherical Co powders (the average particle size is smaller than 0.8m, and
the length-diameter ratio is smaller than 2) with a lower impurity content.
2. Cobalt: Properties, minerals, extraction and applications
2.1. Properties
2.1.1. Physical properties
Cobalt does not occur naturally as a pure metal, but is a component of more than near a
hundred naturally occurring minerals, including various sulfides, arsenides, sulfoarsenides,
hydrates, and oxides. Pure cobalt can be produced by reductive smelting, and was firstly
prepared by G. Brandt in 1735. Cobalt was confirmed as an element by T. Bergman in 1780.
Cobalt is a metallic transition element, and its position in the Periodic Table is characterized:
Energy Conservation 150
Name, symbol, number: Cobalt, Co, 27
Element category: Transition metal
Group, period, block: 9(VIIIA), 4, d
Standard atomic weight: 58.933195
Electron configuration: 4s3d7
Electrons per shell: 2, 8, 15, 2
Co is a brittle, hard metal, resembling iron and nickel in appearance. Pure cobalt produced by
reductive smelting is a hard, lustrous, silver-gray metal. Co has a relative permeability two
thirds that of iron [1]. Its Curie temperature and magnetic moment are 1115C [2] and 1.6~1.7
Bohr magnetons/atom [3], respectively. The basic physical properties are listed in Tab.1, and
vapor pressure vs. temperature is shown in Fig.1. The transformation is sluggish and accounts
in part for the wide variation in reported data on its physical properties. Metallic Co occurs as
two crystallographic structures: a hexagonal closed-packed crystal structure (hcp) and a face-
centered cubic crystal structure (fcc). During cooling, Co usually undergoes a polymorphous
transformation from fcc to hcp. The temperature corresponding to the equilibrium between the
high-temperature (fcc) and low-temperature (hcp) phases in Co is 417C [4], but in fact, the
energy difference is so small that random intergrowth of the two is common [5].
Physical properties values
Color Silver-gray
Density 8.9g/cm
-3
Liquid density at melting point temperature 7.75g/cm
-3
Melting point 1768K, 1495C, 2723F
Boiling point 3200K, 2927C, 5301F
Heat of fusion 16.06kJ/mol
Heat of vaporization 377kJ/mol
Molar heat capacity 24.81J/(molK)
Table 1. The basic physical properties of Co metal
Figure 1. Vapor pressure of Co
Low Energy-Consumption Industrial Production of Ultra-Fine Spherical Cobalt Powders 151
2.1.2. Chemical properties
Pure Co does not dissolve in water and soil, and can stay for years at room temperature (RT).
Co can stay in the air for a few days, and can be oxidized to CoO at about 300C, and can be
burnt to Co3O4 at high temperature. Fine Co powders prepared by the hydrogen-reduction
technology are easily oxidized to cobalt oxide and even generate self-ignite in the air. So the
fine Co powders must be carefully preserved in a vacuum or an inert gas container.
Co is a weakly reducing metal, and is easily attacked by halogens and sulfur, and is also
rapidly dissolved by HCl, H2SO4 and HNO3 acid solution, and is slowly eroded by HF,
NH4OH, NaOH solution.
Co can solid-dissolve many metal and nonmetal atoms to form many intermetallic
compounds. Co can well infiltrate many ceramics (WC, TaC, TiC, ZrC, TiN, Al2O3, cBN,
diamond, etc.), and the almost all wetting angles are lower than 50 [6], so it is often used as
a binder in the above ceramic-metal composites.
2.1.3. Mechanical properties
Metallic Co occurs as two crystallographic structures: hcp- and fcc-. Strength and
hardness of hcp- should be higher than those of fcc-, but inverse for their plasticity
because there are more slipping systems in fcc- than hcp-. Some mechanical properties of
Co are listed in Tab.2.
Mechanical properties
Crystal structures
hcp fcc
Electrical resistivity (m) 6.2410
-8
at 20C -
Thermal conductivity (W/(mK)) 100 -
Thermal expansion (/K) 13.3610
-6
at 25C -
Youngs modulus (GPa) 209 <hcp-Co
Shear modulus (GPa) 75 <hcp-Co
Bulk modulus (GPa) 180 <hcp-Co
Posisson ratio 0.31 -
Vickers hardness (MPa) 1043 <hcp-Co
Table 2. Some mechanical properties of Co
2.2. Co minerals and extraction
Co is not a typically rare metal since it ranks 33 in abundance. Content of Co in the earths
crust is about 0.035wt.%, and about 2.3 billion ton in the sea. Nearly, all Co is always found
associated with metallic-lustered ores of other metals (for example, Cu, Ni, Fe, Pb, Zn, etc.),
and Co minerals without other metals is very less except cobaltite in Morocco. So generally
it is produced as a by-product of other metals mining. Near a hundred cobalt minerals have
been already found in the nature, but about only 20 cobalt minerals are valuable and
available, listed in Tab.3.
Energy Conservation 152
Based on the complexity of the Co minerals, the extraction processing is very complicated
and efficiency of recovery is also very low. As usual, Co in the minerals is firstly
concentrated or is transformed into the soluble states by the pyro-refining, and then Co in
the calcine of pyro-refining is further enriched and extracted by the hydrometallurgy, the
finally the cobalt compounds or pure cobalt are obtained. An extraction processing is shown
in Fig.2 [7]. Section (the production of Co powders) in the dotted line scope in Fig.2 will be
emphasized in the chapter.
Cobalt
minerals
Chemical formula
Theory
cobalt
contents
(wt.%)
Actual
cobalt
contents
(wt.%)
Distribution
Arsenides
CoAs2 23.2 15~21 Canada, Morocco, USA
(Co,Fe)As2 28.2 9~23
Morocco, Canada,
Russian
CoAs3
(Co,Ni)As3 20.8 16~20
Morocco, Canada,
Russian
(Co,Ni,Fe)As3
Sulfides
CoAsS 35.5 29~35.3
China, Canada,
Morocco, USA, Australia
(Co,Fe)AsS 15~20 Morocco
CuCo2S4 38.7 27~42 Zaire, Zambia
Co3S4 48.7 36~53 Zaire, Zambia
(Co,Ni)3S4 26 4~10 USA, China
CoS2 Zaire, China
Oxides
m(Co,Ni)OMnO2nH2O <32 <30
Zaire, China, New
Caledonia
3CoOAs2O38H2O 29.5 Morocco, Canada
CuO2Co2O36H2O 57 45~47 China, Zaire
CoCO3 49.6 Zaire, Zambia
Table 3. Cobalt minerals
2.3. Applications
Due to the excellent physical, chemical, and mechanical properties, it is widely used in
fabricating various alloys (which are used as high-temperature and wear resistant
components, dies, saws, cutting tools, etc.) by powder-metallurgy technology, such as super
alloys, high speed steels, cemented carbides, PCD (polycrystalline diamond) and PCBN
(polycrystalline cubic boron nitride), etc. Co in the above alloys is usually used as an
additive, an alloying element or a binder.
Low Energy-Consumption Industrial Production of Ultra-Fine Spherical Cobalt Powders 153
An important use for Co is in the field of high-temperature alloys. Required in gas turbines,
jet engines, and similar applications, such alloys retain their strength above 650C; these
alloys contain 5~65wt.% Co. Even higher operating temperatures in turbines have resulted
in an increased use of cobalt-containing and cobalt-based alloys known generally as super
alloys. These can withstand severe operating conditions and temperatures up to 1150C. For
example, Nimonic 90 is a nickel-based alloy containing 18wt.% Co, a similar amount of Cr,
and some Ti, and Waspaloy is another alloy of this type.
Figure 2. Cobalt extraction processing (the section in the dotted line scope will be emphasized in the
chapter)
Energy Conservation 154
Cemented carbides, PCD and PCBN are used as cutting tools, wear-resistant components,
dies, saws. In the production of a so-called cemented carbide, i.e. tungsten carbide
composites, a briquetted mixture of tungsten carbide and soft cobalt powders is compacted
and sintered at a temperature above the melting point of cobalt. The latter melts and binds
the hard carbides, giving them the toughness and shock resistance needed to make carbides
of practical value for cutting tools, drill bits, dies, and saws, etc. Co is the most satisfactory
matrix metal for this purpose and may be adjusted in amounts from 3 to 25 percent by
weight. A briquetted mixture of diamond or cBN and Co powders are sintered at high
temperature and high pressure, and PCD and PCBN materials are obtained.
Figure 3. World production trend of cobalt
Very strong magnets are created when Co is alloyed with other metals. So Co is used in
fabricating many advanced magnetic materials.
Cobalts use in rechargeable batteries is the fastest growing use. Notably in 2007, the percentage
of cobalt use for rechargeable batteries rose to 25% of total cobalt demand from 22% in 2006.
World production trend of cobalt is shown in Fig.3 [8,9]. The production of cobalt has been
increasing steadily since 1996.
3. Expectation qualities of cobalt powders in powder metallurgy industry
Powder metallurgy materials (PMM) have been usually fabricated by mixing, pressing, and
sintering processing. The quality (purity, phase, size, shape, dispersity, fluidity, etc.) of raw
powders acts an important role in determining the fabrication and final properties of PMM.
Especially with the rapid development of ultra-fine grain cutting tool materials (such as,
WC/Co alloys, PCBN, PCD, etc.), ultra-fine spherical Co powders (the size is 0.8m and the
length-diameter ratio is smaller than 2) have been desired in order to fabricate a homogeneous
and densified microstructure without pores, Co-pool, Co-poor and Co-free zones, etc.
Though hcp- Co is a room temperature stable phase, fcc- Co can also be steadily retained
at RT by some especial techniques (for example, rapidly cooling). For metal alloys, the
Low Energy-Consumption Industrial Production of Ultra-Fine Spherical Cobalt Powders 155
strength and plasticity are generally contrary, so hcp- and fcc- structures must be
alternative in applications. For cemented carbides (WC/Co alloys), hcp- Co powders are
desired because the cold welding among Co particles due to its higher brittleness can be
decreased during ball-milling. The cold welding (seen as hard agglomerations, as shown
in Fig.4) among Co particles can easily result in Co-pool which result in a rapidly decrease
of mechanical properties of WC/Co alloys. However, fcc- cobalt in the sintered WC/Co
alloys is desired by rapidly cooling during sintering because its good plasticity can improve
the toughness of WC/Co alloys.
(a) Initial morphology (soft agglomeration) of Co particles; (b) Occurring cold welding among fcc- Co particles due
to each other extruding; (c) Forming grain boundaries at the cold welding positions, and forming a hard
agglomeration; (d) Forming flaky Co agglomeration due to plastic deformation; (e) hcp- Co particles well dispersed
Figure 4. Schematic representation of the evolution of hcp- and fcc- Co particle agglomerations
during ball-milling
Energy Conservation 156
4. Decomposition-hydrogen-reduction to fabricate cobalt powders
Co powders in powder metallurgy industry are mainly fabricated by a decomposition-
hydrogen-reduction technique using cobalt compounds of cobalt oxalate (CoC2O42H2O),
cobalt carbonate (CoCO3xH2O), or cobalt oxide (Co3O4) powders as raw materials.
Schematic representation of the device is shown in Fig.5. Raw powders are uniformly tiled
in the boats, and then the boats are pushed into hydrogen-reduction furnace at regular
intervals by a Feeder. The raw powders can also be continuously fed by a conveyor belt in
some companies [10], but we consider that the conveyor belt should carry off a lot of heat,
and resulting in an increase of energy-consumption and the complexity of the device is also
increased. H2 from an inverse direction enters the furnace. The raw powders are heated,
decomposed, and reduced in the heating zone (in which there are usually not less than three
different temperature zones). Obtained Co powders are cooled to RT in the long cooling
zone, and collected into a Receiver, and protected by N2. In order to reduce energy-
consumption and protect the environment, the residual H2 including some other gases, such
as CO, CO2, H2O, etc., is purified by a Purifier, and then reused.
1. Feeder; 2. Boat; 3. H2 exit to a Purifier; 4. Heating zone; 5. H2 entrance; 6. Cooling zone; 7. N2 Protecting; 8. Receiver
Figure 5. Schematic representation of the device used in fabricating Co powder
In order to well understand the decomposition mechanisms of CoC2O42H2O, CoCO3xH2O,
Co3O4 powders and further guide the production of Co powders, their thermal
decomposition kinetics in an inert gas and air will be detailedly studied and discussed in the
following sections. Effect of morphology, size and purity of three raw powders and
technical parameters on the properties of Co powders is also discussed. Some beneficial
methods are also summarized and proposed to improve the quality of Co powders.
4.1. Cobalt oxalate
The chemical formula of the commercial cobalt oxalate is CoC2O42H2O. Fig.6 shows TG and
DTA curves of CoC2O42H2O in an inert gas (such as N2, Ar) and air, respectively. DTA
curve in the inert gas exhibits two endothermic peaks, which are accompanied by the weight
loss of ~19.67% and ~48.09% in the TG curve, respectively. The ranges of reactive
temperatures at the peaks are in about 170~225C and 350~440C, respectively, which will
change a few with different testing conditions (such as changing heating rate). Such weight
loss agrees with the value calculated for the following two transformations:
Low Energy-Consumption Industrial Production of Ultra-Fine Spherical Cobalt Powders 157
2 4 2 2 4 2
CoC O 2H O CoC O + 2H O According to the first endothermic peak (1)
2 4 2
CoC O Co + 2CO According to the second endothermic peak (2)
DTA curve in the air exhibits an endothermic peak and an exothermal peak, which are
accompanied by the weight loss of ~19.67% and ~36.43% in the TG curve, respectively. The
ranges of reactive temperatures at the peaks are in about 170~225C and 270~320C,
respectively, which will also change a few with different testing conditions (such as
changing heating rate). Such weight loss agrees with the value calculated for the following
two transformations:
2 4 2 2 4 2
CoC O 2H O CoC O + 2H O According to the first endothermic peak (3)
2 4 2 3 4 2
3CoC O + 2O Co O + 6CO According to the second exothermic peak (4)
Figure 6. TG and DTA curves of CoC2O4H2O in an inert gas (up) and air (down)
In actual industrial production of Co powders, the decomposition-hydrogen-reduction
processing of CoC2O42H2O occurs in a H2 atmosphere in the device of Fig.5. Tikkanen et al
[11] indicated that the decomposition-hydrogen-reduction processing of CoC2O42H2O was
divided into a guide stage and a decomposition stage. The dehydration (see the reaction (1-
1)) dominates during the guide stage. Huang et al. [12] indicated that high crystallinity
CoC2O4 crystals with less defects can be obtained under a slow dehydration rate, and then
further decomposition processing changes difficulty. Therefore, we easily surmise that it is
disadvantageous to fabricate ultra-fine Co powders due to a decrease of the nucleation rate.
In reverse, CoC2O4 crystals with many defects can be obtained under a rapid dehydration
rate, and then the decomposition changes easy; resulting in an increase of the nucleation
rate. So we propose to increase properly the feeding rate of boat and temperature during the
guide stage. In actual industrial production, we can shorten properly the scope of the I
Energy Conservation 158
heating zone in Fig.5 and increase the dehydration temperature (usually higher 30~50C
than the result of DTA). On the other hand, the dehydration processing of CoC2O42H2O can
be incompletable because hcp- Co powders are easily obtained during the decomposition
of the CoC2O4 with a few H2O.
Fig.7 shows the effect of decomposition temperature and time of CoC2O42H2O on the
specific surface area of Co powders [11]. There are two activation energies for the growth of
Co powders, which implies two different growth mechanisms: the aggregating growth
among Co crystalline nuclei at lower temperature and the second aggregating growth
among Co particles. It is obvious that the second growth must be inhibited during
decomposition. The temperature occurring the second growth is about ~450C, which is
similar to the results of DTA. Therefore, the temperature in the decomposition stage can not
usually be higher than 450C in order to obtain ultra-fine Co powders. In fact, it is very
difficulty to completely inhibit the second growth due to the local overheating in the boat.
The following methods are usually used to improve the temperature homogeneity in the
boat: increasing the surface of the boat, decreasing the layer thickness of CoC2O42H2O
powders, and increasing the flow rate of H2.
Figure 7. Effect of decomposition temperature and time of CoC2O42H2O on the specific surface area of
cobalt powders
Morphology of the commercial CoC2O42H2O powders is a short-fibrous structure with an
average diameter of about 0.5~1m and an average length of about 4~10m, or a bunch
(3~4m) of fibrous particles is formed when several short-fibrous cobalt oxalate particles are
adhered or bonded together during crystallization, as shown in Fig.8(a). Because
morphology of Co powders can easily inherit that of cobalt oxalate, it is very difficulty to
obtain spherical Co powders by decomposing cobalt oxalate; usually replacing a short-string
or dendritic structure, shown in Fig.8(b). Furthermore, the production practice shows that
there is always 2~4% hard agglomeration (a size of 10~30m) in Co powders. The
decomposition processing of cobalt oxalate is schematically shown in Fig.9. The short-
Low Energy-Consumption Industrial Production of Ultra-Fine Spherical Cobalt Powders 159
fibrous CoC2O42H2O particles stacked disorderly in the boat are decomposed and reduced
in situ in the device of Fig.5. The Co nuclei are nucleating and growing to form a short-string
structure along the short-fibrous of CoC2O42H2O particle, and the short-string or dendritic
structure, and even hard agglomerations are formed when several short-string Co
particles grow or bond together.
Figure 8. Morphology of the commercial cobalt oxalate powders and Co powders fabricated by
decomposing cobalt oxalate: (a) short-fibrous cobalt oxatate powders and (b) short-string or dendritic
cobalt powders
(a) Morphology of cobalt oxalate powders; (b) A short-string structure of Co particles along the short-fibrous after
hydrogen-reduction, there is a weak adhesion between Co particles; (c) Co particles grow up, and a strong adhesion
bond between Co particles is formed; (d) The short-string or dendritic structure of cobalt powders after sifting
Figure 9. Schematic representation of in situ decomposition-hydrogen-reduction processing of cobalt
oxalate
In order to obtain ultra-fine spherical cobalt powders, there are two methods: to obtain
spherical cobalt oxalate powders and to impede or break the adhesion of cobalt nuclei
during the decomposing processing of cobalt oxalate. Spherical cobalt oxalate powders can
be crystallized by adding a few spheroidizer [13,14] into the cobalt salt leachate, but the
spheroidizer can deteriorate the properties of the final sintered alloys. Du et al. [15]
proposed that spherical cobalt oxalate powders can be crystallized by adding a pulsed
magnetic field in the cobalt salt leachate, but the size of cobalt oxalate particles is up to
3.5m which is disadvantageous to fabricate ultra-fine Co powders. Huang et al. [16]
proposed to decrease the size of cobalt oxalate powders by an airflow dispersion method,
but it is obvious to largely increase the production cost and to easily result in an increase of
the content of impurity in cobalt oxalate powders. Li et al. [17] proposed to impede the
Energy Conservation 160
adhesion of cobalt nuclei by doping tungsten powders into cobalt oxalate powders, and then
equiaxed or spherical-like Co powders are obtained and the size of Co particles decreases
with increasing tungsten powders. But tungsten can promote to transform hcp-Co into fcc-
Co, and the difficulty controlling the content of carbon in the final sintered WC/Co alloys is
increased because the additional tungsten in Co powders must be completely reacted to
form WC by adding carbon powders.
4.2. Cobalt carbonate
The chemical formula of the commercial cobalt carbonate is CoCO3xH2O (x is lower than 1.).
Fig.10 shows TG and DTA curves of CoCO3xH2O in an inert gas (such as N2, Ar) and air,
respectively. DTA curve in the inert gas exhibits two endothermic peaks. The ranges of
reactive temperatures at the peaks are in about 130~220C and 320~420C, respectively.
According to XRD results in Fig.11, there are the following two reactions:
3 2 3 2
CoCO H O CoCO + H O According to the first endothermic peak x x (5)
3 2
CoCO CoO + CO According to the second endothermic peak (6)
DTA curve in the air also exhibits two obvious endothermic peaks. The ranges of reactive
temperatures at the peaks are in about 130~220C and 250~320C, respectively. According to
XRD results in Fig.11, there are the following two reactions:
3 2 3 2
CoCO H O CoCO + H O According to the first endothermic peak x x (7)
3 2 3 4 2
6CoCO + O 2Co O + 6CO According to the second endothermic peak (8)
Figure 10. TG and DTA curves of CoCO3xH2O in an inert gas (up) and air (down)
Low Energy-Consumption Industrial Production of Ultra-Fine Spherical Cobalt Powders 161
In addition, there seems a weak exothermic peak in about 220~270C, in which the weight
loss on the TG curve is a few slower than that in 270~320C. According to XRD result at
220C in the air, there also are the following two possible reactions:
3 2
CoCO CoO + CO (9)
2 3 4
6CoO + O 2Co O According to the weak exothermic peak (10)
A similar result was reported in Ref. [18], namely the decomposed products of
Co5(OH)6(CO3)2xH2O powders at a lower temperature are a mixture CoO and Co3O4
powders, and CoO is oxidized to form Co3O4 at a higher temperature.
Figure 11. XRD patterns of the decomposed products of CoCO3xH2O powders at various conditions
Being different from the short-fibrous CoC2O42H2O powders, the production practice
[19,20] indicates that the spherical Co powders can be easily obtained by decomposing a
nearly spherical CoCO3xH2O powders (see Fig.12(a)). However, the minimum average size
of Co powders obtained by decomposing CoCO3xH2O powders is only up to 0.8~0.9m (see
Fig.12(b)), and Co powders also possess a wide particle size distribution. The content of fcc-
Co in the powders is as high as 60%.
Another disadvantage is: the content of some impurities (such as S and Ca) in CoCO3xH2O
powders are usually higher than those in CoC2O42H2O powders due to the different
precipitation extraction processing. It is very difficulty to completely eliminate the
impurities, which can be often retained into the final sintered WC/Co alloys. And then the
properties of WC/Co alloys can be deteriorated by the impurities. Fig.13 shows that there is
a higher content of S and Ca at a fracture origin in a sintered WC/Co alloy, and the raw Co
powders are fabricated by decomposing and reducing cobalt carbonate powders. Although
the impurities can be transformed into some non-deleterious compounds by adding a few
Energy Conservation 162
rare earth elements [21,22], the other questions are again introduced during fabricating
WC/Co alloys.
Figure 12. Morphology of (a) the commercial CoCO3xH2O powders and (b) Co powders fabricated by
decomposing and reducing CoCO3xH2O powders
Figure 13. The failure of a sintered WC/Co alloy caused by the S and Ca impurities: (a) A fracture
surface; (b) The EDS analysis at the fracture source (see the square region in (a))
4.3. Cobalt oxide
There are some advantages using Co3O4 powders to fabricate Co powders by hydrogen-
reduction technology: (1) For CoC2O42H2O and CoCO3xH2O powders, Co powders easily
grow if the decomposition and reduction processing (nucleation and growth processing) can
not be completely separated. But for Co3O4 powders, there is only the reduction processing.
So the technology processing is easily controlled. (2) The content of Co in Co3O4 is two times
higher than those in CoC2O42H2O and CoCO3xH2O, as listed in Tab. 4. So the output of Co
powders can be improved by double times at a same reduction condition. (3) The Co
powders obtained by hydrogen-reducing Co3O4 powders are almost all hcp-Co. Therefore,
ultra-fine spherical Co3O4 powders are the best raw material to fabricate ultra-fine spherical
Co powders.
Low Energy-Consumption Industrial Production of Ultra-Fine Spherical Cobalt Powders 163
Compounds CoC2O42H2O CoCO3xH2O CoO Co2O3 Co3O4
Cobalt contents (wt.%) 32.24 49.58 78.67 71.08 73.44
Table 4. Cobalt contents in various raw materials used to prepare cobalt powders
5. The continuous and controllable combustion synthesis
Basing on the above analysis, it is very difficulty to obtain the satisfied ultra-fine spherical
Co powders by the conventional technique while using CoC2O42H2O and CoCO3xH2O as
the raw materials. Ultra-fine spherical Co3O4 powders are the best raw material used to
fabricate ultra-fine spherical Co powders. But the key question is how to obtain ultra-fine
spherical Co3O4 powders by a low energy-consumption and low-cost method? And then a
continuous and controllable combustion synthesis has been proposed.
5.1. Basic principles
5.1.1. Selecting the raw powders
As mentioned above, although spherical Co powders can be obtained by decomposing
spherical CoCO3xH2O powders, there is the higher content of some impurities (such as S
and Ca) and the size of Co powders is still larger. So CoC2O42H2O powders will be used as
the raw materials to fabricate ultra-fine spherical Co3O4 powders, and then ultra-fine
spherical Co powders can obtained by hydrogen-reduction technology in Fig.5. Using
CoC2O42H2O powders to fabricate ultra-fine spherical Co3O4 powders, the following
advantages can be utilized and some key technical difficulties must be resolved.
5.1.2. Utilizing the exothermal reaction of CoC2O42H2O Low energy-consumption
Selecting CoC2O42H2O powders as the raw material to fabricate ultra-fine Co3O4 powders, a
main advantage is that the decomposition processing of CoC2O42H2O in the air is an
exothermal processing according to DTA. Seham et al. [23] showed that the total exothermal
energy was 24.26kJ/mol during the decomposition of CoC2O42H2O in the air, which is an
enough energy to operate the following decomposition processing of CoC2O42H2O.
Therefore, after giving a starting energy, the decomposition once starts, and then further
heating does not need, and the needful energy of the following decomposition can be
provided by the released reaction energy of CoC2O4 converting into Co3O4. So the
decomposition processing of CoC2O42H2O in the air is a spontaneous and continuous
processing, and a lot of energy can be saved.
5.1.3. Utilizing airflow dispersion to in situ break the adhesion among Co3O4 particles
Morphology of Co3O4 powders can still inherit the short-fibrous structure of CoC2O42H2O
powders when the decomposition processing is carried out in a fixed bed, namely Co3O4
particles can easily grow together to form a short-fibrous structure (see Fig.14(a)) due to the
exothermal reaction. But a short-fiber is composed of ultra-fine spherical Co3O4 particles
Energy Conservation 164
with a size of about 0.1~0.2m, see Fig.14(b). The Co3O4 particles arrange a short-string
along to the fiber, and there is a weak adhesion between particles. The results further
explain why the short-string or dendritic Co powders is easily obtained by decomposing
and reducing CoC2O42H2O powders in a fixed bed. Ultra-fine Co3O4 powders with the size
of 0.1~0.2m can obtained if the weak adhesion between them before forming a strong bond
can be broken in situ. How to break the adhesion of Co3O4 particles? So a dynamic
decomposing processing is proposed. If an airflow can be provided to CoC2O42H2O
powders during decomposition, the released energy can be homogenized to avoid overheat
in part and also impede the adhesion and grow among Co3O4 particles.
Figure 14. The short-fibrous structure of Co3O4 particles obtained by decomposing CoC2O42H2O
powders in a fixed bed: (a) low multiple, the morphology with a short-fibrous structure is very similar
to that of CoC2O42H2O powders; (b) Magnifying several fibrous particles, consisted of ultra-fine
spherical Co3O4 particles with a size of about 0.1~0.2m
5.2. Production equipments
According to the above desires, a continuously dynamic-controlled combustion synthesis
(CDCCS) process is proposed and the bottlenecks of continuous production and process
controls of combustion synthesis (CS) have also been solved satisfactorily. The
preparation of ultra-fine Co3O4 powders via CDCCS is carried out in a gas-solid fluidized
bed unit (CS unit), as shown in Fig.15. The unit is patented equipment consisting of
fluidized bed roaster, feeding systems, receiving systems, dust collection systems and air
supply system [24,25].
There are reaction and cooling boiling (11 and 21) that formed by gas-solid fluidization on
the upper and lower gas distribution plates (61 and 62), respectively. The raw material on
the upper gas distribution plate (61) is fleetly penetrated by the gas from the upper gas
pipeline (32). The boiling bed with the flowing property like liquid is formed when the
superficial gas velocity reaches a critical value of 0.03m/s. In our experiments, the superficial
gas velocity is 0.09~0.18m/s. The height of boiling beds, locating between the gas
distribution plates to the top of overflow gates, is about 500mm. And several thermocouples
are installed on the CS unit wall and the location is about at 2/3 height of boiling beds.
Low Energy-Consumption Industrial Production of Ultra-Fine Spherical Cobalt Powders 165
When the boiling bed (11) containing CoC2O42H2O powders which are fed into by the screw
feeder (51) is preheated to 380C by the hot carrier gas, CoC2O42H2O powders will react
with O2 in the air. Co3O4 powders pour from the upper overflow pipe (35) under gravity and
enter the cooling boiling bed (21), followed by collecting from the lower overflow pipe (34).
The temperature of CS in reaction region can be perfectly controlled though the linkage of
the upper thermocouple (71) and the upper gas pipeline (32).
Figure 15. Schematic representation of CS unit, in which Co3O4 powders fabricated by CDCCS: 1.
Fluidized bed roaster; 10. Upper chamber; 11. Reaction boiling bed; 12. Upper overflow gate; 13. Feed
inlet; 19. Clapboard; 20. Lower chamber; 21 Cooling boiling bed; 22. lower overflow gate; 23. Overflow
entry; 31. Upper exhaust pipe; 32. Upper gas pipeline; 33. Lower gas pipeline; 34. Lower overflow pipe;
35. Upper overflow pipe; 36. Lower exhaust pipe; 41. Upper dust catcher; 42. Lower dust catcher; 43.
Product collection container; 51. Screw feeder with storage hopper; 61. Upper gas distributor; 62. Lower
gas distributor; 71. Upper thermocouple; 72. Lower thermocouple
5.3. Process analysis of CDCCS to fabricate Co3O4 powders
When the reactant CoC2O42H2O powders are fed by the screw feeder (51) into the boiling
bed, no self continuous reaction occurs. Only when CoC2O42H2O powders in the
combustion zone are heated by hot carrier gas, and the continuous reaction is ignited. This
means that once the combustion reaction between O2 and CoC2O42H2O powders is ignited,
the released heat by the combustion reaction can be used to ignite the following exothermic
reaction and no external heat is needed, and then the hot carrier can be transformed into the
cool carrier gas.
Energy Conservation 166
Fig.16 shows the effect of the feeding rate of CoC2O42H2O powders and the superficial gas
velocities in the boiling bed on the temperature of combustion wave [26]. Temperature of
combustion wave decreases with increasing gas velocity at a given feeding rate. Therefore,
the temperature of combustion wave can be adjusted and controlled dynamically by
changing the feeding rate of CoC2O42H2O powders and/or the superficial gas velocity.
According to the thermal analysis of CoC2O42H2O in the air, the CoC2O4 can be completely
converted to Co3O4 at a temperature higher than 320C. Therefore, in order to ensure the
dehydration reaction of CoC2O42H2O and the oxidation reaction of CoC2O4 can be carried
out rapidly and completely, and the combustion temperature is set at 380~400C.
Figure 16. Effect of the feeding rate of CoC2O42H2O powders and the superficial gas velocities in the
boiling bed on the temperature of combustion wave
Being different from the conventional CS, the combustion wave here is almost full of the
combustion zone in the middle of the boiling bed and the temperatures in whole space are
homogeneous. The combustion wave is relatively suspended in the fluidized bed, and the
temperature in the combustion zone can be dynamically controlled by adjusting the flow of
carrier gas, as mentioned above. During the preparation, CoC2O42H2O powders are
continuously fed by the screw feeder into the upper area of reaction boiling bed and
contacted with the combustion wave. The Co3O4 particles are dispersed by the carrier gas
flow. After the CS, the dispersed Co3O4 powders fall down and leave the combustion wave
in time through flowing out off the overflow gate on the wall of the unit continuously.
The CS unit in the paper is different from the conventional one reported in Ref. [27,28]. In
the conventional unit, the reactants and products are nearly stationary while the combustion
wave propagates from reactants to products. The advantages of the continuous fluidization
technologies and the CS are well utilized and combined in our unit. The combustion wave is
relatively stationary, but the reactants and products are continuous and mobile at a given
speed.
Low Energy-Consumption Industrial Production of Ultra-Fine Spherical Cobalt Powders 167
5.4. Quality of products
Fig.17(a) shows the morphology of Co3O4 powders fabricated by the CDCCS. The adhesion
among Co3O4 powders shown in Fig.14(b) is broken by the carrier gas flow. The particles
exhibit a spherical or quasi-spherical shape, and the size of Co3O4 particles is about
0.1~0.3m. In the gas-solid fluidized bed unit, the temperature of the whole boiling bed is
nearly homogeneous, and almost each solid particle in the boiling bed has a similar
surrounding, namely all CoC2O42H2O particles can be completely decomposed to form
Co3O4. The suspended solid particles collide and grind each other without aggregation by
the action of airflow, which accelerates the formation of the spherical Co3O4 powders. The
uneven distributions of particle size or hard aggregation appear scarcely due to the
favorable diffusion condition and rapid transfer of heat and mass. The Co3O4 powders with
a narrow particle size distribution, good dispersity and excellent fluidity are fabricated by
the CDCCS.
As mentioned above, using the ultra-fine spherical Co3O4 powders fabricated by the CDCCS
as raw materials, the ultra-fine spherical or quasi-spherical Co powders is easily obtained by
hydrogen-reduction technology, as shown in Fig.17(b). The Co powders with an average
size of 0.6m possess a narrow particle size distribution, good dispersity, and excellent
fluidity.
Figure 17. (a) Ultra-fine spherical Co3O4 powders fabricated by CDCCS; (b) Ultra-fine spherical Co
powders fabricated by hydrogen-reduction technology using ultra-fine spherical Co3O4 powders as raw
materials
Energy Conservation 168
5.5. Advantages of the CDCCS
The preparation of ultra-fine spherical Co3O4 powders (the size is smaller than 0.8m and
the length-diameter radio is smaller than 2) by the CDCCS has been successfully applied in
the industrialization production in Xiamen Golden Egret Special Alloy Co., Ltd [24,25].The
novel method has the following several advantages:
1. Comparison with the fixed bed, ultra-fine spherical Co3O4 powders are continuously
produced in the fluidized bed unit and the production efficiency is improved.
2. No external heat is needed after the reaction is once ignited, and then the energy
consumption is reduced.
3. The fabrication process is in a closed unit so that a clean operation environment is
realized and a high pure product is fabricated.
4. The device operations are automated, except the transport of reactants and products,
thus the labor intensity is largely decreased.
5. The most important advantage is that the properties of the products fabricated by
CDCCS are more excellent than those fabricated by the conventional method.
6. Expectation
Ultra-fine spherical Co3O4 powders are firstly fabricated by CDCCS, and then ultra-fine
spherical Co powders can be fabricated by hydrogen-reduction technology. Can ultra-fine
spherical Co powders be directly fabricated by CDCCS if a hydrogen flow is blown into
the CS unit? However, the hydrogen is a flammable and explosive gas. Therefore, our
future work is how to directly fabricate ultra-fine spherical Co powders in the CS unit by
solving the key technology difficulty of the hydrogen safety. Furthmore, the fabrication of
many other metal powders (for example, W, Mo powders, etc.) can be applied in the CS
unit.
Author details
Chong-Hu Wu
China National R&D Center for Tungsten Technology,
Xiamen Tungsten Co. Ltd. Technology Center, Xiamen, China;
Xiamen Golden Egret Special Alloy Co. Ltd., Xiamen, China
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[17] Wei Li, Qin-sheng Zhao. Research on characteristic properties of tungsten-doped cobalt
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[18] Yi-yong Yang, Ju-tang Sun, Liang-jie Yuan, Ke-li Zhang. Micro-method powder X-ray
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Energy Conservation 170
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Chapter 7
Production and Characterization of Biofuel from
Non-Edible Oils: An Alternative Energy
Sources to Petrol Diesel
A.S. Abdulkareem, A. Jimoh, A.S. Afolabi, J.O. Odigure and D. Patience
Additional information is available at the end of the chapter
http://dx.doi.org/10.5772/51341
1. Introduction
The production and consumption of petroleum oil increases constantly and it has been
reported that about 75 million barrels of crude oil is consumed worldwide daily [1-4].
Resulting energy crisis as a result of over dependence on fossil fuel as a source of energy
have shown that fossil fuels are limited finite resource and the continuous depreciation of
the world oil reserves also corroborates the fact that oil is a finite non-renewable source of
energy that will ultimately be exhausted [5-9]. This therefore leads to continuous agitation
and research activities towards establishing alternative renewable fuels that can replace and
prevent possible negative impacts that may result from continuous use and depreciation of
fossil fuel [10]. The need to reduce complete dependence on fossil fuel as a sole energy
sources and need to source for alternative energy cannot be over emphasized. Presently,
biofuel, biogas and bio ethanol are considered as the most promising alternatives in energy
generation that can compete with the fossil fuel [2, 11-12]. Biodiesel is produced in some
countries and used efficiently either alone or in blends with minerals diesel in cars and
transport vehicles. The transesterification of the triglycerides present in plant oils to the
methyl or ethyl esters. Since the passage of the Energy Policy Act of 2005, biodiesel use has
been increasing especially in the developed countries. For instance, biodiesel is produced in
some countries and used efficiently either alone or in blends with mineral diesel in cars and
transport vehicles [13]. The United State Fueling stations make biodiesel readily available to
consumers across Europe and increasingly in the USA and Canada. This is an indication that
biodiesel can operates in compression ignition engines like petroleum diesel without
requiring no essential engine modifications [14-16]. Moreover it can maintain the payload
capacity and range of conventional diesel unlike fossil diesel, pure biodiesel is
Energy Conservation
172
biodegradable, nontoxic and essentially free of sulphur and aromatics [17-19]. A growing
number of transport fleets use it as an additive in their fuel. Biodiesel is being used in both
public and private fleet vehicles due to environmentally friendly and the facts that it offers a
reduction in some emissions without requiring any modifications to the vehicle of biodiesel
[14]. It is worth of mentioning that the production of this alternative energy source
(biodiesel), which is a variety of ester-based oxygenated fuels, can be produced from
different feedstock, such as vegetable oil, animal fats and non edible oils [20-24]. Hence, the
production of biodiesel is sensitive to feedstock; care must therefore take in selecting the
feed stock for the production of biofuel [14]. For instance production of biofuel from vegetable
oils had been criticized by the experts as a source of food crisis [14]. The critics of this method
of biofuel production beliefs that production of biofuel from consumable oil will resulted into
food crisis and price instability. Also militate against the commercial availability of biodiesel is
the cost of biodiesel. For instance, biodiesel costs over US$0.5/l compared to US$0.3/l for petrol
diesel, the is due mainly to the cost of virgin vegetable oil used as a feedstock for the
production of biodiesel [14]. For instance, in the United State, the cost of soybean is on the
average of US$0.36/l, Currently, the cost of biodiesel stands at 3.83 dollars per gallon which is
19.6% higher compared to that of petro-diesel ($ 3.07) [25]. It is therefore not surprising that the
biodiesel produced from pure soybean is much more expensive than petroleum based diesel.
Hence, the recent research and development in the production of biofuel as alternative energy
sources that will compete well with the existing energy sources (fossil fuel) is now
concentrated on in-edible oil, which is the focus of this present study [26-31]. This work
involves comparative study of biodiesel production from Jatropah curcas and Ricininus
communis. The choice of Jatropha curcas and Ricinus communis as a feedstock for the
production of biodiesel is also favoured by the abundantly availability of these plants in
Nigeria, despite their abundant availability, they are not properly exploited for technological
and material development. Hence, Production of biodiesel from these oils will lead to proper
utilization of these vegetable oils. It also includes characterization of both the oils and biodiesel
produced. The focus of this study can be achieved through the following objectives;
Characterization of both jatropha curcas and ricinus commumis oils to determine
density, viscosity, saponification number, iodine value, acid value, peroxide value and
moisture content which are compared with the standard.
Production of biodiesel from jatropha curcas and ricinus commumis by two-step
transesterification reaction.
Investigation into the effect of temperature and catalyst concentration on the
production of biodiesel from oil.
Characterization of the biodiesel produced to determine the density, flash point,
Kinematic viscosity, Cloud point, Sulphur content, Bottom Sediment & Water, Cetane
number, water by distillation and distillation properties and compare with that of
convention diesel fuel and available standard.
Comparison of the qualities of biodiesel produced from Jatropha curcas and Ricinus
communis with that of the standard values of biodiesel
Production and Characterization of Biofuel from Non-Edible Oils:
An Alternative Energy Sources to Petrol Diesel
173
1.1. History of biodisel
The name biodiesel has been given to transesterified vegetable oil to describe its use as a
diesel fuel. Transesterification of triglycerides in oils is not a new process. Scientists E. Duffy
and J. Patrick conducted it as early as 1853 [11, 32]. Rudolf Diesel's prime model, a single
10 ft (3 m) iron cylinder with a flywheel at its base, ran on its own power for the first time in
Augsburg, Germany, on 10 August 1893 running on nothing but peanut oil. In remembrance
of this event, 10 August has been declared "International Biodiesel Day". Life for the diesel
engine began in 1893 when the famous German inventor Rudolph Diesel published a paper
entitled the theory and construction of a rational heat engine. What the paper described
was a revolutionary engine in which air would be compressed by a piston to a very high
pressure thereby causing a high temperature. Rudolph Diesel designed the original diesel
engine to run on vegetable oil [14,32]. Dr Rudolph Diesel used peanut oil to fuel one of his
engines at the Paris Exposition of 1900. The engine was constructed for using mineral oil,
and was then worked on vegetable oil without any alterations being made. The French
Government at the time thought of testing the applicability to power production of the
Arachide, or earth-nut, which grows in considerable quantities in their African colonies, and
can easily be cultivated there." Diesel himself later conducted related tests and appeared
supportive of the idea [32]. Due to the high temperatures created, the engine was able to run
a variety of vegetable oil including hemp and peanut oil. At the 1911 Worlds Fair in Paris,
Dr R. Diesel ran his engine on peanut oil and declared the diesel engine can be fed with
vegetable oils and will help considerably in the development of the agriculture of the
countries which use it. One of the first uses of transesterified vegetable oil was powering
heavy-duty vehicles in South Africa before World War II [32]. In a 1912 speech Diesel said,
"The use of vegetable oils for engine fuels may seem insignificant today but such oils may
become, in the course of time, as important as petroleum and the coal-tar products of the
present time." Despite the widespread use of fossil petroleum-derived diesel fuels, interest
in vegetable oils as fuels for internal combustion engines was reported in several countries
during the 1920s and 1930s and later during World War II. Belgium, France, Italy, the
United Kingdom, Portugal, Germany, Brazil, Argentina, Japan and China were reported to
have tested and used vegetable oils as diesel fuels during this time [32]. Some operational
problems were reported due to the high viscosity of vegetable oils compared to petroleum
diesel fuel, which results in poor atomization of the fuel in the fuel spray and often leads to
deposits and coking of the injectors, combustion chamber and valves. Attempts to overcome
these problems included heating of the vegetable oil, blending it with petroleum-derived
diesel fuel or ethanol, pyrolysis and cracking of the oils [14]. Research into the use of
transesterified sunflower oil, and refining it to diesel fuel standards, was initiated in South
Africa in 1979 [32]. By 1983, the process for producing fuel-quality, engine-tested biodiesel
was completed and published internationally. An Austrian company, Gaskoks, obtained the
technology from the South African Agricultural Engineers; the company erected the first
biodiesel pilot plant in November 1987, and the first industrial-scale plant in April 1989
(with a capacity of 30,000 tons of rapeseed per annum) [32].
Energy Conservation
174
Throughout the 1990s, plants were opened in many European countries, including the
Czech Republic, Germany and Sweden. France launched local production of biodiesel fuel
(referred to as diester) from rapeseed oil, which is mixed into regular diesel fuel at a level of
5%, and into the diesel fuel used by some captive fleets (e.g. public transportation) at a level
of 30%. Renault, Peugeot and other manufacturers have certified truck engines for use with
up to that level of partial biodiesel; experiments with 50% biodiesel are underway. During
the same period, nations in other parts of the world also saw local production of biodiesel
starting up: by 1998, the Austrian Biofuels Institute had identified 21 countries with
commercial biodiesel projects. 100% Biodiesel is now available at many normal service
stations across Europe [32]. In September 2005 Minnesota became the first U.S. state to
mandate that all diesel fuel sold in the state contain part biodiesel, requiring a content of at
least 2% biodiesel [32]. Todays diesel engines require a clean burning and stable fuel that
performs well under the variety of operating condition. Biodiesel is the only alternative
fuel that can be used directly in any existing unmodified diesel engine. It has been
reported that biodiesel can be blended with the diesel fuel in any proportion due to the
similarities in their properties and the current trends in the production of biodiesel from
vegetable are now concentrated on non- edible oil as the feedstock. Vegetable oils such as
soybean, rapeseed and peanut are edible and expensive though the seeds of these oils are
available in large quantities especially in Africa (Tamil Nadu -641 003india) [32]
.However, there is need to control their utilization for the production of biodiesel for the
purpose of not causing large problem of hunger and deforestation while sourcing for
alternative energy sources [33-35].
1.2. Biodiesel
Biodiesel is defined as the mono-alkyl esters of fatty acids derived from a renewable lipid
feedstock such as vegetable oils or animal fats [2, 16, 36-37]. In simple terms, biodiesel is the
product obtained when a vegetable oil or animal fat is chemically reacted with an alcohol to
produce fatty acid alkyl esters. A Catalyst such as sodium or potassium hydroxide is
required. Glycerol is produced as a co product. Vegetable oils are a renewable and
potentially inexhaustible source of energy with a calorific value close to that of conventional
diesel fuel. Their high viscosity, low volatility, incomplete combustion and possibility of
formation of deposits are the drawbacks of biodiesel. Biodiesel besides not being refined
from crude oil, biodiesel offers other attractive characteristics, such as a significantly lower
emission of carbon monoxide, CO (46.7 %,) carbon dioxide, CO2, (78%), [38], sulphur
dioxide, SO2 and hydrocarbons, HC (45.2%) [39]. It also eliminates the cloud of dense, black
smoke normally associated with diesel vehicles and other particulate matter (PM) emissions
(66.7%) that cause respiratory damage to a level in line with the Kyoto Protocol Agreement
[40]. Biodiesel is also reported to be highly biodegradable in freshwater as well as soil
environments. 9098% of biodiesel is mineralized in 2128 days under aerobic as well as
anaerobic conditions in comparison to 50% and 56% by diesel fuel and gasoline respectively
[41]. European tests of rape seed oil-based biodiesel indicate that it is 99.6% biodegradable
Production and Characterization of Biofuel from Non-Edible Oils:
An Alternative Energy Sources to Petrol Diesel
175
within 21 days [42]. Thus within one month of being spilled into the environment, biodiesel
should be completely decomposed. This makes biodiesel a good alternative fuel for use in
environmentally sensitive areas where fuel leakages and spills would be particularly
harmful such as wetland areas and watersheds which supply drinking water. It has been
reported also that biodiesels have high cetane number, high flash point and acceptable level
of sulphur content which makes it very attractive as an alternative fuel [43]. Reported work
by Korbitz (1999) [44] shows that the cetane number of biodiesel fuels is higher than fossil
diesel which is considered to be significantly advantageous in terms of engine performance.
The flash point of biodiesel fuels is twice as much as that of fossil diesel. Therefore, biodiesel
is much safer to store, handle and use than the conventional diesel fuel [45]. Biodiesel fuels
have been praised as being sulphur-free and may contain only traces of sulphur emanated
from the acidic catalyst used. Also favour the choice of biodiesel as alternative sources of
energy is the fact that biodiesel is virtually compatible with commercial diesel engines and
practically no engine modifications are required [46]. Biodiesel can also be blended at any
level with petroleum diesel to create a biodiesel blend. When blended with fossil diesel, it
shows positive synergic effect of biodegradation by means of co-metabolism. For example,
the time taken to reach 50% biodegradation of fossil diesel is reduced from 28 to 22 days in
5% biodiesel mixture [47]. In terms of economic benefit, biodiesel production is expected to
remain profitable and grow dramatically. Farmers that produce highly rated energy crops
such as Jatropha for the production of biodiesel stand a chance of improving their income
level by providing market outlets for farmers and generate rural employment. The by-
product of transesterification reaction, glycerol, when purified can be used in its traditional
application (pharmaceutical, cosmetics and food industries). In addition, the obtained
glycerol can be used in recently developed applications in the fields of animal feed, carbon
feedstock in fermentations, polymers, surfactants and lubricants [48]. Biodiesel, thus,
increases the contribution of agriculture to exports and economic growth. It will also
generate new industries which will create new jobs and new markets for the majority of
unemployed youth [49].
Despite the advantages of biodiesel as perfect alternative energy sources, emission of NOx is
one of the setbacks of biodiesel. The temperature within the cylinders of a vehicle fuelled
with biodiesel would increase due to the enhanced combustion as a result of high oxygen
content of biodiesel. This increase in temperature stimulates the production of NOx from the
reaction with nitrogen in the air, which results in a small increase in NOx emission
compared to those produced from conventional diesel fuel [50]. Aside from the formation of
NOx by the engine powered with biodiesel, the chemical contents of biodiesel is also a fatty
acid methyl ester when the alcohol used during transesterification is methanol or fatty acid
ethyl ester in case of ethanol. These ester molecules are susceptible to hydrolytic and
oxidization reactions resulting in the formation of polymers. This makes the biodiesel
unstable on storage and hence cannot sit on the shelf for long time as it develops mould
when it gets old [51]. Exploring the means of producing biodiesel that will compete well
with the existing petroleum diesel is of much interest in the recent biodiesel research,
especially for those methods concentrating on minimizing the raw material cost. Biodiesel as
Energy Conservation
176
alternative energy source can be produced from different sources such as soybean, beef
tallow, waste vegetable oil etc depends on the location and availability. The fact that
biodiesel burns clearly and source from renewable sources widens its acceptance world
wide as alternative energy source. Biodiesel which is described as variety of ester-based
oxygenated fuels derived from natural, renewable sources such is a perfect alternative
energy sources due to its biodegradability nature. To improve the quality of vegetable oil,
researchers have employed different methods listed below to reduce the high viscosity of
the oils.
1. Dilution of 25 parts of vegetable oil with 75 parts of diesel fuel (biodiesel blends)
2. Micro emulsions with short chain alcohol (e.g. ethanol or methanol).
3. Thermal decomposition which produces alkanes, alkenes, carboxylic acids and aromatic
compounds.
4. Catalytic cracking which produces alkanes, cycloalkanes and alkyl benzene.
5. Transesterification.
Transesterification is described as the best choice as it is relatively simple and produces a
product with properties close to diesel fuel. Alcohol, oil and catalyst are combined in an
agitated reactor, approx. at 60C during 1h. Smaller plants often use batch mode reactors,
but larger plants use continuous flows processes involving continuous stirred-tank reactors
or plug flow reactors. The processes involved in biodiesel production from feedstock
containing low levels of FFA which, include soybean oil, canola (rapeseed) oil, and the
higher grades of waste restaurant oils. Alcohol, catalyst, and oil are combined in a reactor
and agitated for 1hour at 60C. Smaller plants often use batch reactors [32] but most larger
plants (4 million L/yr) use continuous flow processes involving continuous stirred-tank
reactors (CSTR) or plug flow reactors [32]. The reaction is sometimes done in two steps in
which 80% of the alcohol and catalyst is added to the oil in a first-stage CSTR. Then, the
product stream from this reactor goes through a glycerol removal step before entering a
second CSTR. The remaining 20% of the alcohol and catalyst is added in this second reactor.
This system provides a very complete reaction with the potential of using less alcohol than
single-step systems. After the reaction, glycerol is removed from the methyl esters. Due to
the low solubility of glycerol in the esters, this separation generally occurs quickly and can
be accomplished with either a settling tank or a centrifuge. The excess methanol tends to act
as a solubilizer and can slow the separation. However, this excess methanol is usually not
removed from the reaction stream until after the glycerol and methyl esters are separated
due to concern about reversing the transesterification reaction. Water may be added to the
reaction mixture after the transesterification is complete to improve the separation of
glycerol [32].After separation from the glycerol, the methyl ester enter a neutralization step
and then pass through a methanol stripper, usually a vacuum flash process or a falling film
evaporator, before water washing. Acid is added to the biodiesel product to neutralize any
residual catalyst and to split any soap that may have formed during the reaction. Soaps will
then react with the acid to form water-soluble salts and FFA. The salts will be removed
during the water washing step and the FFA will stay in the biodiesel. The water washing
step is intended to remove any remaining catalyst, soap, salts, methanol, or free glycerol
Production and Characterization of Biofuel from Non-Edible Oils:
An Alternative Energy Sources to Petrol Diesel
177
from the biodiesel. Neutralization before washing reduces the amount of water required
and minimizes the potential for emulsions to form when the wash water is added to the
biodiesel. After the wash process, any remaining water is removed from the biodiesel by a
vacuum flash process. The glycerol stream leaving the separator is only 50% glycerol. It
contains some of the excess methanol and most of the catalyst and soap. In this form, the
glycerol has little value and disposal may be difficult. The methanol content requires the
glycerol to be treated as hazardous waste. The first step in refining the glycerol is usually to
add acid to split the soaps into FFA and salts. The FFA is not soluble in the glycerol and will
rise to the top where they can be removed and recycled[32]. Mittelbach and Koncar [32]
described a process for esterifying these FFA and then returning them to the
transesterification reaction stream. The salts remain with the glycerol, although depending
on the chemical compounds present, some may precipitate out. One frequently touted
option is to use potassium hydroxide as the reaction catalyst and phosphoric acid for
neutralization so that the salt formed is potassium phosphate, which can be used for
fertilizer. After acidulation and separation of the FFA, the methanol in the glycerol is
removed by a vacuum flash process, or another type of evaporator. At this point, the
glycerol should have a purity of 85% and is typically sold to a glycerol refiner. The glycerol
refining process takes the purity up to 99.599.7% using vacuum distillation or ion exchange
processes. Therefore, biodiesel is defined as the mono-alkyl esters of fatty acids derived
from vegetable oils, animal fats by transesterification with alcohol in the presence of
catalyst. A catalyst such as sodium or potassium hydroxide is required; glycerol is produced
as a by-product.
2. Jatropha curcas and ricininus communis (castor oil) and biodiesel
production
2.1. Jatropha curcas
Jatropha is a drought resistance tree that can be grown in areas where rainfall is as low as
500-600mm. It does well in Cape Verde where rainfall is only 250mm but the air is humid. In
dry season, it tends to shed its leaves. Where rainfall is high above 1000mm, it does better in
hot rather than temperate climate. Jatropha grow in soils that are quite infertile. It is usually
found at lower elevations (below 500m) (14,32]. Jatropha Curcas is mostly found in northern
part of Nigeria e.g. Sokoto, Zamfara, Kebbi, Kastina Minna etc [32].
There is growing interest for biodiesel production from non-edible oil source, like Jatropha
curcas . Jatropha curcas is a plant belonging to Euphorbiaceae family, which is a non-edible
oil-bearing plant widespread in arid, semi-arid and tropical regions of the world[32].
Jatropha curcas has an estimated annual production potential of 200 thousand metric tons in
India and can grow in waste land [32]. Jatropha curcas is native to Mesoamerica but has
been distributed worldwide since the XVI century by Spaniards and Portuguese to their
tropical and subtropical colonies in Africa and Asia. In India and other countries of the Far
East, villagers used Jatropha curcas as a hedge crop, and the extracted seed oil to make soap
Energy Conservation
178
or fuel for lamps. In Europe, biodiesel production is based on the methyl ester of rapeseed
oil, while in the United States, the methyl esters of soybean and rapeseed oils are more used.
In tropical countries, Jatropha curcas seed oil is being promoted for biodiesel production,
and the technology has been optimized [51]. It was found that the shell could be for
combustion, hull/husk for gasification, and cake for production of biogas, spent slurry as
manure, oil and biodiesel (made from Jatropha oil) for running CI engines. The kernels ) of
jatropha curcas have about 50% oil. The oil recovery in mechanical expeller was about 85%,
while more than 95% recovery of oil could be achieved when extracted by solvent method.
The biodiesel from jatropha curcas oil has a great potential due to its comparable properties
to diesel, such as calorific value and cetane number [51]. Therefore, many researchers have
shown great interest in using Jatropha oil to produce biodiesel. Azam et al. (2005) [52] found
FAME of Jatropha curcas were most suitable for use as biodiesel and it met the major
specification of biodiesel standards of USA, Germany and European Standard Organization.
Sarin et al. ( 2007) [51] made 25 appropriate blends of Jatropha and palm biodiesel to
improve oxidation stability and low temperature property based on the fact that Jatropha
biodiesel has good low temperature property and palm biodiesel has good oxidative
stability. It was found that antioxidant dosage could be reduced by 80-90% when palm oil
biodiesel is blended with Jatropha biodiesel at about 20-40%. This techno-economic
combination could be an optimum mix for Asian Energy Security. Tiwari et al. (2007) [53]
used response surface methodology to optimize three important reaction variables,
including methanol quantity, acid concentration, and reaction time. The optimum
combination for reducing the FFA of Jatropha oil from 14% to less than 1% was found to be
1.43% v/v sulfuric acid catalyst, 0.28 v/v methanol-to-oil ration and 88 min reaction time at
60C for producing biodiesel. The properties of Jatropha oil biodiesel conformed to the
American and European standards. As comparison, Berchmans et al. (2008) [54] developed a
two-step pretreatment process in which the high FFA (15%) of Jatropha curcas seed oil was
reduced to less than 1%. In the first step, the reaction was carried out with 0.60 w/w
methanol-to-oil ratio in the presence of 1 wt.% sulfuric acid as an acid catalyst in 1h at 50C.
In the second step, the transesterification reaction was performed using 0.24 w/w methanol-
to-oil ratio and 1.4 wt.% sodium hydroxide as alkaline catalyst to produce biodiesel at 65C.
The final biodiesel yield of 90% in 2hours was reported. As well as experimental study,
theoretical studies of reaction mechanism were also conducted regarding to base-catalyzed
transesterification of the glycerides of the Jatropha oil (Tapanes, Aranda, Carneiro &
Antunes, 2008). In that study, semi-empirical AM1 molecular orbital calculations were used
to investigate the reaction pathways of base, catalyzed transesterification of glycerides of
palmitic, oleic and linoleic acid. The researchers concluded that the reaction mechanism
included three steps: Step 1- Nucleophilic attack of the alkoxide anion on the carbonyl group
of the glyceride to form a tetrahedral intermediate. Step 2-Breaking of the tetrahedral
intermediate to form the alkyl ester and the glyceride anion. Step 3-Regeneration of the
active catalyst, which may start another catalytic cycle. This study suggested that the Step 2,
decomposition of the tetrahedral intermediate, determined the rate of base-catalyzed
Production and Characterization of Biofuel from Non-Edible Oils:
An Alternative Energy Sources to Petrol Diesel
179
transesterification of glycerides. A lot of different approaches were taken when producing
biodiesel from Jatropha oil. In additional to conventional methods, preparation of biodiesel
from Jatropha oil using ultrasonic energy was investigated (Kachhwaha, Maji, Faran, Gupta,
Ramchandran & Kumar, 2006). Low frequency ultrasound (33 kHz) was applied to
transesterify Jatropha oil with methanol in the presence of base catalyst at 6:1 methanol/oil
molar ratio. The reaction time (about 15-30 min) was much shorter than conventional
mechanical stirring method. This method was proved to be efficient and economically
functional. Moreover, enzyme catalysts were also utilized for biodiesel production from
Jatropha oil. Shah et al. Jatropha oil in presence of supercritical carbon dioxide. The optimum
conditions were found to be 8h, 45C, 5:1 molar ratio of alcohol to oil and an enzyme loading
of 30% based on the weight of oil. However, conversions of only 60-70% were obtained even
after 8 hours. The authors attributed this to the fact that the enzymatic reaction encountered
both substrate and product inhibition. In contrast, when synthesis of biodiesel in
supercritical alcohols, high conversions (80%) were obtained within 10 min and nearly
complete conversions were obtained within 40 min. Despite of expected high operating cost
due to high temperature and pressure associated with supercritical alcohol, it was still
considered to be economically feasible since the reaction time was very short [32].
Furthermore, the absence of pre-treatment step, soap removal, and catalyst removal can
significantly reduce the capital cost of a biodiesel plant. Meanwhile, many researches were
conducted aiming at evaluating the performance, emission, and combustion characteristics
in a diesel engine for Jatropha oil and Jatropha oil biodiesel [32] .Haldar et al. (2008) [55]
found that Jatropha oil gave the best results related to the performance and emissions, such
as CO, CO2, HC, smoke and particulates, at high loads and 45 before Top Dead Center
(BTDC) injection timing when compared with non-edible straight vegetable oils of
Putranjiva, Jatropha and Karanja. Though received a booming interest due to its general
characteristics and potentiality was recommended by some researchers that better data are
urgently needed to guide investment since uncertainty do exist, based on the fact that
Jatropha curcas is still a wild plant which exhibits a lot of variability in yield, oil content and
oil quality [32].
2.2. Ricininus communis (castor oil)
Castor oil is possibly the plant oil industrys most underappreciated asset. It is one of the
most versatile of plant oils, being used in over ten diverse industries. Owing to its unique
chemical structure, castor oil can be used as the starting material for producing a wide range
of end-products such as biodiesel, lubricants and greases, coatings, personal care and
detergent, surfactants, oleo chemicals e.t.c. Compared to many other crops, castor crop
requires relatively fewer inputs such as water, fertilizers and pesticides. The crop can also be
grown on marginal land, thus providing an excellent opportunity for many regions of the
world to utilize their land resources more productively [32]. The plant prefers well-drained
moisture relative clay or sandy loan in full sun requires a rich soil and day time temperature
above 20
o
C for seedling to grow well. Castor is native to tropical Africa but it grows widely
Energy Conservation
180
in Nigeria as weed it can be found in Borno, Sokoto, Jos, Zaria and so many other places in
the country [32]. Though, it has been reported that the plants is not properly exploited,
however a fiber for making ropes can be obtained from its stem. The growing plant is said to
repel flies and mosquitoes when grown in the garden and it is also said to rid it of moles
and nibbling insect, while the leaves have insecticidal properties.
Cultivation of castor plants for the production of biodiesel started in 2008 in the Waletia and
Goma Gofa regions of Ethiopia, the initiative is run by energy company (Global energy
Ethiopia) who are also conducting research and development program to create new
varieties of castor with better yields(sub-sahara Africa gateway, science and development
network, 2008). Castor oil contains a number of fatty acids similar to those in cooking oils
such as oleic, palmitic acids e.t.c. However, among vegetable oils castor oil is distinguished
by its high content of ricinoleic acid (about 89.5 %). Castor oil unsaturated bond, molecular
weight (298), low melting point (5 C) makes it industrially useful. Castor oil is unique
among all fats and oils, it has an unusual composition of a triglyceride of fatty acids, and it
is the only source of an 18-carbon hydroxylated fatty acid with one double bond (Aldrich,
2003). The chemical composition of castor oil is given below [32]:
Ricinoleic acid - 89.5 %
Linoleic acid - 4.2 %
Oleic acid - 3 %
Stearic acid - 1 %
Palmitic acid - 1 %
Dihydroxystearic acid - 0.7 %
Exosanoic acid - 0.3 %
Biodiesel derived from castor oil rates high among other oils with ash content of about 0.02
%, sulfur content less than 0.04 %, negligible potassium content, 35 GJ/T which compares
favorably with other vegetable oils and petro diesel of about 45 GJ/T, and viscosity that is
much higher than petro diesel, but this major bottleneck of the viscosity can be considerably
reduced by transesterification making it a very efficient source of biodiesel
3. Material and methodology
3.1. Material and equipment
This study focus on the conversion of oil from Jatropha Curcas and Ricininus communis
(castot oil) into biodesel by means of eseterification. The entire chemicals used in this study
are of analytical grade (98-99.5%). They include Carbon tetra chloride (Analar, BDH), Wijs
solution (Mixture of glacial acetate, iodine trichloride and carbon tetralchloride) (Hopkins
and Williams, London), potasium hydroxide solution (Analar, BDH), potassium hydroxide
pellet (Burgoyne & co, India), petroleum ether (Analar, BDH), potassium iodide solution
(M&B, England), sodium thisosulphate (M&B, England), hydrochloric acid (Analar, BDH)
and potassium iodide pellet (M&B, England). The equipments used are pH meter,
Production and Characterization of Biofuel from Non-Edible Oils:
An Alternative Energy Sources to Petrol Diesel
181
distillation apparatus, viscometer, thermostatic hot plate, sulphur in oil analyzer, magnetic
stirrer, digital weighing balance, thermometer, petri dish, pippete, separating funnel, burete,
oil test centrifuge, pycometer bottles, Abbe refractometer, flash point tester, oven and
aneline point teseter.
3.2. Methodology
3.2.1. Physical and chemical characterization of the oil
Prior to the production of biodiesel from jatropha cacus and risininus communis (castor oil),
various anlysis such as specific gravity, acid value, free fatty acid, saponification value,
iodine value, peroxide value, viscosity, moisture content and refarctive index were
conducted on the oil samples.
3.2.1.1. Determination of specific gravity
A 50ml pycometer was washed thoroughly with detergent, water and petroleum ether, it
was then dried and weighed. The bottle was filled with water and weighed, the bottle was
then dried and filled with the oil sample and weighed, from theory, and the density of a
substance was equal to mass of a substance per unit volume of that substance.
3.2.1.2. Determination of Acid Value/Free Fatty Acid (FFA)
2g of the oil was measured and poured in a beaker. A neutral solvent (a mixture of
petroleum ether and ethanol) was prepared and 50ml of it was taken and poured into the
beaker containing the oil sample. The mixture was stirred vigorously for 30minutes. 0.56g of
potassium hydroxide (KOH) pellet was measured and placed in a separate beaker and 0.1M
KOH was prepared, 3drops of phenolphthalein indicator was added to the sample and was
titrated against 0.1M KOH till the color change observed turned pink and persisted for
15minutes.
Av =
56.1 v N
w
OIL
(1)
Where; V= volume of standard alkali used; N= normality of standard alkali used; Woil=
weight of oil used
FFA =
AN
2
(2)
3.2.1.3. Determination of saponification value
The alcoholic KOH was freshly prepared by dissolving KOH pellet in ethanol. 2g of oil was
measured and poured into a conical flask. 25ml of the alcoholic KOH was added to it, a
blank was used. The sample was well covered and placed in a steam water bath for
30minutes shaking it periodically, 1ml of phenolphthalein was added to the mixture and
titrated against 0.5M HCl to get the end point.
Energy Conservation
182
Sv =
5.61 (B-A)N
w
OIL
(3)
Where; B= volume of standard ethanol potassium hydroxide used in blank titration; A=
volume of standard ethanol potassium hydroxide used in titration with the oil; N=
normality of standard acid; Woil= weight of oil used.
3.2.1.4. Determination of iodine value
The oil was poured into a small beaker, a small rod was added to it.2g of the oil was
weighed and poured into a glass-stopper bottle of about 250 ml capacity. 10ml of carbon
tetrachloride was added to the oil to dissolve. 20ml of Wijs solution was added and a
stopper was inserted and allowed to stay in the dark for 30minutes. 15ml of potassium
iodide solution (10%) and 100ml of water was introduced and the mixture was thoroughly
mixed and titrated with0.1M sodium thiosulphate solution using starch as indicator
(titration = Aml). A blank was carried out at the same time starting with 10ml of carbon
tetrachloride (titration = Bml)
Iv =
0.1269 (B-A) N 100
w
OIL
(4)
B= volume of sodium thiosulphate used in blank titration.
A= volume of sodium thiosulpate used in titration with oil.
N= normality of sodium thiosulphate.
Woil= weight of oil used.
3.2.1.5. Determination of peroxide value
1g of oil was weighed into a clean drying boiling tube, 1g of powdered potassium iodide
and 20ml of solvent mixture (2volume of glacial acetic acid + 1volume of chloroform) was
added, the tube was placed in boiling water so that the liquid boils within 30seconds and
was also allowed to boil vigorously for not more than 30seconds. The content was quickly
poured into a flask containing 20ml of potassium iodide solution; the tube was washed out
with 25ml of distilled water and was titrated with 0.002M sodium thiosulphate solution
using starch as indicator. A blank was also carried out at the same time.
3.2.1.6. Determination of viscosity
A viscometer was used to determine the viscosity of the oil. Chloroform was poured first in
the viscometer and the time at which the chloroform reached the bottom of the equipment
was taken. The oil was then poured into the viscometer and the time taken far the
groundnut oil to reach the bottom of the equipment was taken and recorded in mm
2
/s
3.2.1.7. Determination of moisture content
In other to determine the moisture content in the oil (%), 48.15g of oil was weighed in a
moisture pan, the weight of the pan and oil was taken and was put inside an oven for
3hours at a temperature of 45
0
C. After every 1hour, the sample was cooled and weighed
until the weight before and after was approximately equal.
Production and Characterization of Biofuel from Non-Edible Oils:
An Alternative Energy Sources to Petrol Diesel
183
3.2.1.8. Determination of refractive index
Abbes refractometer was used to determine the moisture content of the oil sample, the
equipment was well cleaned with cotton wool and placed in a bright room for light. The
refractometer was calibrated using distilled water then small sample of the oil was placed
on it and the refractive index observed was taken and recorded.
3.2.2. Two-step transesterification of the crude oils
In order to avoid the problem of saponification, a two-step method was used for synthesis of
biodiesel from Jatropha curcas and Ricinus communis.
3.2.2.1. Acid catalyzed esterification
This is considered as a pre-treatment for the crude oils in order to reduce their water content
which is the main cause of soap formation and subsequently, reduce its FFA. The oil was
heated in the reaction glass tube to 65
o
C and a solution of concentrated H2SO4 acid (1.0%
based on the oil weight) in methanol (30% v/v) was heated to 45
o
C and added to the reaction
glass tubes. The resulting mixture was stirred on a magnetic stirrer for 1hr and the content
was poured into a separating funnel and allowed to settle for 2 hours. The methanol-water
fraction at the top layer was removed and the oil was decanted to be used for
transesterification reaction.
3.2.2.2. Alkali catalyzed transesterification
50ml of oil was measured and poured into a 150ml conical flask and heated to a temperature
of 45
o
C using a water bath. A solution of sodium methoxide was prepared in a 250ml beaker
using 0.25g of NaOH pellet and 10.5mls of anhydrous methanol. The solution was properly
stirred until the NaOH pellet was completely dissolved in it. The sodium methoxide
solution was then poured into the warm oil and stirred vigorously for 90minutes using a
magnetic stirrer and the mixture was left to settle for 24hours in a separating funnel. After
settling, the upper layer which was biodiesel was decanted into a separate beaker while the
lower layer which comprises of glycerol and soap was collected from the bottom of the
funnel. The quantity of biodiesel collected was measured and recorded.
3.2.3. Washing
Biodiesel must be washed to remove any remaining methanol, glycerin, catalyst, soaps and
other impurities. Water used is warmed to about 45
0
C and is passed through the esters to
allow soluble material, excess catalyst and other impurities to stick to the water and be
settled to the bottom of the vessel. The water is removed from the vessel periodically until
the wash water drained out is clear or the pH of the biodiesel becomes relatively neutral.
3.2.4. Drying
The biodiesel washing sometimes leaves the biodiesel looking a bit cloudy. This means
there's still a little water in it. It was heated slowly to 100
o
C and held there until all moisture
present was evaporated i.e. dry.
Energy Conservation
184
3.2.5. Characterization of the biodiesel produced
3.2.5.1. Determination of specific gravity/density (ASTM D1298) by hydrometer method
This procedure is used to measure of specific gravity of the biodiesels. A clean dry empty
50ml density bottle is to be weighed and the mass recorded as M, it is then filled up with
distilled water and subsequently with the samples. The mass of the bottle and water is taken
and recorded as M1 and that of biodiesel as M2 respectively hence, the specific gravity is
evaluated. This procedure is used to determine the specific gravity of the sample.
3.2.5.2. Determination of flash point: ASTM D 93 Flash-point by Pensky-Martens
closed cup tester
A sample of the biodiesel is heated in a close vessel and ignited. When the sample burns, the
temperature is recorded; the pensky-martens cup tester measures the lowest temperature at
which application of the test flame causes the vapor above the sample to ignite. The
biodiesel is placed in a cup in such quantity as to just touch the prescribed mark on the
interior of the cup. The cover is then fitted onto the position on the cup and Bunsen burner
is used to supply heat to the apparatus at a rate of about 5
o
C per minute. During heating, the
oil is constantly stirred. As the oil approaches its flashing, the injector burner is lighted and
injected into the oil container after every 12 second intervals until a distinct flash is observed
within the container. The temperature at which the flash occurred is then recorded, it is
repeated three times and the average taken.
3.2.5.3. Determination of cloud point (ASTM D 2500)
A sample of the biodiesel is placed in a test jar to a mark and then placed inside a cooling
bath. The temperature at the bottom of the test jar that is the temperature at which the
biodiesel starts to form cloud is taken as the cloud point.
3.2.5.4. Determination of kinematic viscosity (ASTM D 445)
A viscometer is inserted into a water bath with a set temperature and left for 30minutes. The
sample is added to the viscometer and allowed to remain in the bath as long as it reaches the
test thermometer. The sample is allowed to flow freely and the time required for the
meniscus to pass from the first to the second timing mark is taken using a stop watch. The
procedure is repeated a number of times and the average value are taken which is then
multiplied with the viscometer calibration to give the kinematic viscosity.
3.2.5.5. Determination of pour point (ASTM D 97)
A sample of the biodiesel is kept in the freezer to about 50
0
C then placed in a heating mantle
to melt. The temperature at the bottom of the test jar that is the temperature at which the
biodiesel starts to pour is taken as the pour point.
3.2.5.6. Cetane Number (ASTM D 613)
Cetane Number is a measure of the fuel's ignition delay. Higher Cetane numbers indicate
shorter times between the injection of the fuel and its ignition. Higher numbers have been
Production and Characterization of Biofuel from Non-Edible Oils:
An Alternative Energy Sources to Petrol Diesel
185
associated with reduced engine roughness and with lower starting temperatures for
engines.
3.2.5.7. Acid Number (ASTM D 664)
The biodiesel sample is measured and poured in a beaker. A neutral solvent (a mixture of
petroleum ether and ethanol) is prepared and 50ml of it is taken and poured into the beaker
containing the biodiesel. The mixture is stirred vigorously for 30minutes. 0.56g of potassium
hydroxide (KOH) pellet is measured and placed in a separate beaker and 0.1M KOH is
prepared, 3drops of phenolphthalein indicator is added to the sample and is titrated against
0.1M KOH till the color change observed turned pink.
3.2.5.8. Determination of sulphur content (ASTM D 5453)
The sulphur content was determined by the energy dispersive X-ray fluorescence
spectroscopy technique. The biodiesel was placed in disposable plate covered with male and
female cells; the sample was placed in a oil in sulphur test equipment and left for 10minutes.
The equipment measures the sulphur content of the biodiesel three (3) consecutive times
and takes the average which is then recorded as the sulphur content.
3.2.5.9. Determination of distillation characteristics (ASTM D 86)
The distillation characteristics were studied using distillation apparatus (Model PMD 100) in
accordance to the procedure in ASTM D 86. 100ml of the biodiesel was charged into the
distillation flask. A thermometer provided with a snug-fitting cork was tightly fitted into the
neck of the distillation flask. The flask was then fixed tightly into the condenser tube by
raising and adjusting the flask support board of a calibrated distillation batch unit.
Systematic observations and recordings of temperature readings at 5mls, 10mls, 20mls,
30mls, 40mls, 50mls, 60mls, 70mls, 80mls, and 90mls respectively, and volumes of
condensate were taken and recorded.
3.2.5.10. Determination of bottom water and sediment (ASTM D 2709)
The water and sediment test was determined according to ASTM D 2709, 50mls of the
biodiesel and 50ml of toluene were mixed in a 100ml centrifuge tube with the tube tip
having graduation of 0.01ml over the range of 0 to 0.2ml, the centrifuge tube was shaken so
that an even distribution of the mixture is observed. The tube was placed in a trunnion cup
inside an oil test centrifuge in such a way that the tubes are placed opposite each other to
establish a balance in the centrifuge. The centrifuge is then closed and timed for 30 minutes;
the samples are then whirled for agitation at a speed of 1800rpm to ensure homogeneity.
The combined water and sediment at the bottom of the tube was reported to the nearest
0.005ml.
4. Results and discussion of results
Concern on the situation of fossil fuel as the sole sources of energy and environmental
pollution emanated from the utilization of fossil fuel resulted into considerable attention
Energy Conservation
186
given to alternative sources of energy. Biodiesel is considered as a perfect alternative source
of energy that can compete with fossil fuel in terms of performance and efficiency. However,
production of biodiesel from vegetable oils and animal fats also raised a serious concern of
food crisis and the critics of the production of biodiesel from edible are making it difficult to
justify the use of edible oil for fuel, considering the tremendously increment in demand for
edible oil. Hence the need to produce biodiesel from non-edible oils such as Jatropha Curcas
and Ricinus Communis oil that are grown in large quantities and waste lands in Nigeria,
which is the focus of this study. Results obtained on characterization of the oils and
biodiesel produced from the non-edible oils are hereby presented.
4.1. Physiochemical properties of Jatropha curcas and Ricinus communis oil
Ricinus communis and Jatropha Curcas oils that were utilised as a feedstock in the
production of biodiesel were characterized to determine their physiochemical properties
such as density, pH, viscosity, acid value, iodine value etc. The results obtained on the
properties of oils were compared with that of American Oil Chemists Society (AOCS)
standard values and the results obtained are presented in Table 1. The iodine value shows
the level of unsaturation of the oil and also influences the oxidation and deposition formed
in diesel engines. It is used in determining the drying property of the oil. Iodine value
obtained for both Jatropha curcas and Ricinus communis were seen to be 98gI2/100g and
85gI2/100g respectively and both values fall within the acceptable AOCS limit as shown in
Table 1. The iodine value of Jatropha (98 gI2/100g) was seen to be higher than that of Ricinus
(85 gI2/100g) and this signifies that there is a higher degree of unstauration in the former
than in the latter, although, both oils are classified as non-drying oils since their iodine value
is below 115 gI2/100g. Moisture in vegetable oils is a great impediment to the formation of
esters due to increase in tendency of soap formation and thus will have to be minimal for
transesterification to occur [14]. The moisture content in both Jatropha curcas and Ricinus
communis were seen to be 0.20% and 0.24% respectively and are within the range specified
by AOCS as shown in Table 4.0. The moisture content of Jatropha curcas (0.20%) was seen to
be a little less than that of Ricinus communis (0.24%) and this signifies a higher content of
water in Ricinus communis than Jatropha curcas. The saponification value of oil is a
measure of the tendency of the oil to form soap during the transesterification reaction. The
saponification value obtained for Jatropha curcas and Ricinus communis were seen to be
190mgKOH/g and 178mgKOH/g respectively and are within the range specified by AOCS
as shown in Table 1. The saponification value of Jatropha curcas (190mgKOH/g) was seen to
be a bit higher than that of Ricinus communis and this thus signifies a higher tendency of
the former forming soap during transesterification reaction than the latter. Vegetable oils
with high acid value are classified as inedible while those with low acid value are classified
as edible oils. The acid value obtained for both Jatropha curcas and Ricinus communis were
seen to be 36.8mgKOH/g and 0.913mgKOH/g respectively and both values fall within the
acceptable AOCS limit as shown in Table 1. Leung and Guo (2006) [56] reported that oils
with high acid value tend to deactivate catalyst used during transesterification and the acid
value of Jatropha (36.8mgKOH/g) was seen to be exceedingly higher than that of Ricinus
Production and Characterization of Biofuel from Non-Edible Oils:
An Alternative Energy Sources to Petrol Diesel
187
(0.913mgKOH/g) and this signifies that the ester yield of Jatropha curcas will be less than
that of Ricinus communis due to increase catalyst deactivation and soap formation in the
former. Also, the same can be said for the free fatty acid (FFA) present in both with their
values being 18.4% and 0.457% respectively. Kinematic viscosity which is a measure of the
flow capabilities of the oils was measured at 30
o
C. The kinematic viscosity of Jatropha curcas
and Ricinus communis were seen to be 51.8mm
2
/s and 6.9mm
2
/s respectively and both are
within the range specified by AOCS as shown in Table 1. The kinematic viscosity of Jatropha
curcas (51.8mm
2
/s) was seen to be extremely higher than that of Ricinus communis
(6.9mm
2
/s) and this means that Ricinus communis has a higher flow capability than Jatropha
curcas and can easily undergo transesterification.
Parameters Unit Obtained
Expt Value
for Jatropha
Curcas
Obtained
Expt Value
for Ricinus
Communis
AOCS
Standard
Value for
Jatropha
Curcas
AOCS
Standard
Value for
Ricinus
Communis
Saponification
Value (S.V)
mgKOH/g 190 178 188-195 176-184
Iodine Value
(I.V)
gI2/100g oil 98 85 84-100 83-88
Acid Value
(A.V)
mgKOH/g 36.8 0.913 1.0-38.2 2.0 max
Free Fatty
Acid (FFA)
% 18.4 0.457 <1% <1%
Specific
Gravity (S.G)
at 30
o
C
- 0.913 0.89 0.910-0.915 0.88-0.915
Density () g/ml 0.856 - -
Refractive
Index (R.I) at
30
o
C
- 1.466 1.468 1.467-1.470 1.467-1470
Kinematic
Viscosity (v)
at 30
o
C
mm
2
/s 51.8 6.9 - 6.3-8.9
Moisture
Content
% 0.20 0.24 - 0.355 %
max
Table 1. Comparison of Physiochemical Properties of Ricinus communis and Jatropha curcas oils with
AOCS standard values
4.2. Optimization of two-step transesterification of Jatropha curcas and Ricinus
communis
Transesterification is the reaction between triglycerides and lower alcohols to produce free
glycerols and the fatty acid ester. It involves reaction between the oil which is the feedstock
Energy Conservation
188
and an alcohol, usually methanol in the presence of a catalyst such as sodium or potassium
hydroxide to give corresponding esters. Although, the main factors influences the
transesterification reactions are the alcohol to oil molar ratio, catalyst type and
concentration, reaction temperature and reaction time, with the methanol to oil ratio higher
than stoichiometrix ratio to drive the equilibrium to a maximum ester yields. However, in
this present study all other factors are kept constant except the temperatures that are
varying between 50
o
C to 60
o
C. Sodium hydroxide was selected as the catalyst, the ratio of oil
to methanol was 1:6, reaction time was 60 minutes and the weight of catalyst was 0.5wt%.
Results obtained on the effect of temperature on the yield of biodiesel from Jatropha Carcus
and Ricinus Communis oil as the feed stock are presented in Table 2. The best yields were
obtained for both the methyl ester of Jatropha curcas and Ricinus communis at the
temperature of 60
o
C with the percentage methyl ester yield being 96% and 98%. This is
because at 60
o
C, the molecules of the triglycerides of Jatropha curcas and Ricinus communis
had high kinetic energy and this thus increased the collision rate and therefore, improved
the overall process by favouring the formation of methyl esters while at the lower
temperatures of 50
o
C and 55
o
C with corresponding percentage methyl ester yield of 86%
and 90% and 92% and 95% respectively, there was lesser collision of reacting molecules and
thus, reduced biodiesel yield as seen in Table 2. The reason for this behaviour is due to the
endothermic nature of the reaction. The higher reaction temperature would favour
endothermic reaction, thus increasing the rate of reaction as well as the ester concentration.
Although at 65
o
C, it was noticed that there was a drop in percentage methyl ester yield for
both Jatropha curcas and Ricinus communis as shown in Fig 4.0 below with their
corresponding values being 84% and 86% respectively. This is because at the reaction
temperature (65
o
C), there was increased vaporization of the alcohol (methanol) used in the
transesterification process due to the proximity of the reaction temperature (65
o
C) to the
boiling point of methanol (64.7
o
C). Based on the results obtained on the effect of
temperature on the yield of biodiesel, it can be deduced that the optimum conditions for the
production of methyl ester from crude Jatropha curcas and Ricinus communis through two-
stage transesterification are oil to methanol molar ratio of 1:6, catalyst concentration of
0.5wt%, reaction time of 60 minutes and reaction temperature of 60
o
C.
Temperature
(
o
C)
Jatropha curcas
Production
Yield (wt%)
Jatropha curcas
Methyl Ester
Yield (wt%)
Ricinus communis
Production Yield
(wt%)
Ricinus communis
Methyl Ester Yield
(wt%)
50
55
60
65
89
94
99
90
86
92
96
84
93
98
99
92
90
95
98
86
Table 2. Effect of Temperature on Biodiesel Yield from Jatropha curcas and Ricinus communis
4.3. Characterization of produced esters
The biodiesel produced from Jatropha curcas and Ricinus communis using the optimal
conditions of 1:6 oil to methanol molar ratio, 0.5wt% catalyst concentration, 60 minutes
Production and Characterization of Biofuel from Non-Edible Oils:
An Alternative Energy Sources to Petrol Diesel
189
reaction time and reaction temperature of 60
o
C were analyzed for their fuel properties. Their
properties were compared to the ASTM D 6751 biodiesel standard and the ASTM D 975
fossil diesel standard in order to confirm their acceptability as fuel in diesel engines as
shown in Table 3. Kinematic viscosity is a measure of resistance to flow of a liquid due to
internal friction of one part of the fluid moving over another. High viscosity affects the
atomization of a fuel upon injection into the combustion chamber and thus leads to the
formation of engine deposits [57]. The kinematic viscosities of Jatropha curcas and Ricinus
communis were determined to be 4.93mm
2
/s and 14.2mm
2
/s respectively and when
compared to ASTM D 6571, it was seen that the viscosity of Jatropha falls within range while
that of Ricinus communis is far from the acceptable standard, although, it falls within the
acceptable limit of fossil diesel (ASTM D 975) as presented in Table 3. It can be therefore said
that the methyl esters of Ricinus communis has a higher tendency of forming deposits in
engines than that of Jatropha curcas due to the significant difference in kinematic viscosity
and this makes Jatropha curcas methyl ester a more suitable fuel as regards viscous
property. The flash point is the lowest temperature at which an applied ignition source will
cause the vapours of the fuel to ignite. It is therefore a measure of tendency of a sample to
form a flammable mixture with air. The flash point obtained for Jatropha curcas and Ricinus
communis were 142
o
F and 150
o
F respectively and they fall within the range of standard limit
set by ASTM D 6751 (130
o
F min) [58]. Ricinus communis has a higher flash point when
compared to Jatropha curcas, but both are considerably high and this leads to their safer
handling and storage. Cloud point and pour point have implications on the use of biodiesel
in cold weather applications. The cloud point is the most common measure of the tendency
of a fuel to crystallize and the cloud point of Jatropha curcas and Ricinus communis were
determined as 5
o
C and 8
o
C respectively. This signifies that Ricinus communis has a high
tendency of forming cloudy crystals easily in cold temperature than Jatropha curcas.
Biodiesel is also potentially subject to hydrolytic degradation caused by the presence of
water. Fuel contaminated with water can cause engine corrosion and breakdown. From the
results obtained, Jatropha has traces of bottom sediment and water while Ricinus communis
has 0.05%vol and both values conforms to the ASTM D 6751 set standard whose maximum
allowable limit is 0.05%vol. Since Jatropha curcas methyl ester has a neglible amount of
bottom water and sediment, it is of better quality compared to Ricinus communis. Sulfur in
the atmosphere has negative impacts on human health and on the environment and
biodiesel have traditionally been acknowledged as sulfur-free which is of great advantage
over fossil diesel and the results obtained confirms that fact. The sulfur content of both
Jatropha curcas and Ricinus communis were 0.05%wt and 0.03%wt which is within the
ASTM D 6751 standard limit (0.05 max). Also, the sulphur content of the methyl ester of
Jatropha was seen to be higher than that of Ricinus and this signifies that the latter is more
environmentally friendly than the former. Elevated total glycerine values are indicators of
incomplete esterification reactions and predictors of excessive carbon deposits in the engine.
This can be as a result of incomplete washing of the ester after production. The free
glycerine is a source of carbon deposits in the engine because of incomplete combustion. The
free and total glycerines determined for the methyl ester of Jatropha curcas and Ricinus
communis were 0.02wt% and 0.24wt% and 0.02wt% and 0.23wt% respectively and both
values were seen to be within the acceptable standard of ASTM D 6751. On comparison with
Energy Conservation
190
each other, they were found to be approximately equal. Generally, the cetane number is a
dimensionless descriptor of the ignition quality of a diesel fuel. As such, it is a prime indicator
of diesel fuel quality. The cetane number of the methyl esters of Jatropha curcas and Ricinus
communis were found to be 46.11 and 50.64 respectively. On comparison with standard, it was
found that the cetane number of that of Jatropha curcas was below the allowable minimum of
47 stated by ASTM D 6751 while that of Ricinus communis was slightly above it. On further
comparison with fossil diesel standard, it was seen that the centane number of both was above
the allowable minimum of 40 imposed by ASTM D 975. Thus results confirm the fact that
biodiesels generally, have a higher cetane number than fossil diesels
Property Unit ASTM
Test
Method
Expt.
Value
for
Jatropha
curcas
Expt.
Value for
Ricinus
communis
ASTM
Standard
for
Biodiesel
(ASTM
D 6751)
ASTM
Standard
for Petrol
diesel
(ASTM D
975)
Kinematic
Viscosity at 40
o
C
mm
2
/s D 445 4.39 5.42 1.9-6.0 1.9-4.1
Density/Specific
Gravity
kg/l D 1298 0.88 0.88 0.86-0.89 0.95 max
Flash Point
o
F D 93 142.0 150.0 93.0 min 150 min
Cloud Point
o
F D 2600 41.0 46.4 40 max
Total Sulphur
(X-Ray)
% wt D 4294 0.05 0.03 0.05max 0.50 max
Bottom Water &
Sediment
% vol D 1796 Trace 0.05 0.05 max 0.50 max
Distillation
Properties
IBP
o
C D 86 128 302 360 max -
FBP
o
C 329 360 205 max
Total Recovery % 98 97
Centane
Number
- D 975 46.11 50.64 47 min 40 min
Water by
Distillation
% vol D 95 Trace 0.05 - 0.5 max
Free Glycerine %
mass
D 6584 0.02 0.02 0.02 max 0.02 max
Total Glycerine %
mass
D 6584 0.24 0.23 0.24 max 0.24 max
Table 3. Fuel Properties of Jatropha curcas and Ricinus communis Methyl Esters
Boiling point is the temperature at which a liquid transition to a gas and it is also related to
the flash point. For a pure substance the boiling point is a single temperature value.
Production and Characterization of Biofuel from Non-Edible Oils:
An Alternative Energy Sources to Petrol Diesel
191
However, for a mixture of hydrocarbons as existing in biodiesel fuel, there is a range of
boiling points for the different constituent chemical specie. The data tested for in the methyl
ester of Jatropha curcas and Ricinus communis includes the initial boiling point (IBP),
boiling temperature corresponding to increments of the volume of fuel distilled (10%, 20%,
30%, 40%, 50%, 60%, 70%, 80% and 90%), final boiling point (FBP) and % total recovery
(Table 4) .
Percentage Recovery (cm
3
) Temperature (
o
C)
Jatropha curcas Ricinus communis
IBP 128 302
10% 234 307
20% 255 309
30% 260 312
40% 290 322
50% 313 330
60% 321 336
70% 326 343
80% 328 350
90% 329 360
FBP 329 362
% Total Recovery 97.77 97.00
Table 4. Distillation Characteristic Table of Jatropha curcas and Ricinus communis Methyl Esters
5. Conclusion
The need to move away from oil as a major source of energy is growing every year, due to
the price instability and environmental pollution which are the consequence of over
dependence on the fossil fuel. The current research and development on alternative energy
that will replace fossil fuel is now focusing on the biofuel. Renewable biofuel will reduce the
dependence on oil and also reduce the trade deficit of nations, especially the developing
nations. However, for biofuel to compete with the fossil fuel and possibility replacing it as
the energy source, needs to be easy, cheap and fast to produce. Production of biofuel from
vegetable oil is however not economical due to the fact that production of biodiesel from
vegetable will lead to food crisis while trying to solve energy crisis. It is therefore much
more desirable to use non-edible oils as a feedstock in the production of biodiesel, which is
the focus of this study. This study report the production of biodiesel from non-edible oils
(Jatropha Carcus and Ricinus Communis) as alternative to petrol diesel. Based on the results
of experimental analysis, it can be concluded that oils from both feed stocks are suitable for
the production of biodiesel. Also, temperature had a high effect on biodiesel yield and the
yield increased with increasing temperature up to a point where the reacting temperature
was proximal to the boiling point of the methanol. It can also be concluded that, though,
Ricinus communis had a higher methyl ester yield (98wt%) than Jatropha Carcus (96wt%) at
Energy Conservation
192
same optimal reaction conditions, the methyl ester of Jatropha Carcus is a more suitable fuel
for diesel engines than that of Ricinus communis because the fuel properties obtained for
the former were more compatible with the engines and in accordance with ASTM D 6751
than that of the latter.
Author details
A.S. Abdulkareem
*
Department of Chemical Engineering, School of Engineering and Engineering Technology,
Federal University of Technology, PMB 65 Minna, Niger State, Nigeria
Department of Civil and Chemical Engineering, College of Science, Engineering and Technology,
University of South Africa, Private Bag X6, Florida 1710, Johannesburg, South Africa
A. Jimoh, J.O. Odigure and D. Patience
Department of Chemical Engineering, School of Engineering and Engineering Technology,
Federal University of Technology, PMB 65 Minna, Niger State, Nigeria
A.S. Afolabi
Department of Civil and Chemical Engineering, College of Science, Engineering and Technology,
University of South Africa, Private Bag X6, Florida 1710, Johannesburg. South Africa
Acknowledgement
Support received from Step B Project, Federal University of Technology, Minna Nigeria is
highly appreciated. National research foundation (NRF), South Africa and Faculty of
Science, Engineering and Technology, University of South Africa are also appreciated for
their support.
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Chapter 8
Production and Characterization of
Biofuel from Refined Groundnut Oil
A. Jimoh, A.S. Abdulkareem, A.S. Afolabi, J.O. Odigure and U.C. Odili
Additional information is available at the end of the chapter
http://dx.doi.org/10.5772/52443
1. Introduction
Persistent global energy and fuel crises have shown that fossil fuels are limited source of
energy that will ultimately get exhausted [1-3]. Continuous depreciation of the world oil
reserves as reported by USEIA (2007) [4] also corroborates the fact that fossil fuels resources
like petroleum, coal and natural gas are finite and non-renewable source of energy. Apart
from the foreseen shortage of fossil fuels, its rising price and increasing difficulty of paying
for them in the next years to come, necessitate the serious urge for alternative resource that
will offers reduced emissions, improved biodegradability, improve performance and clean
up emissions necessitated continuous research into the development of renewable energy
source. Aside the fact that gasoline and diesel are the most widely used fuels coming from
fossil fuel [5], it is a known fact now that gasoline contributes to increase hazardous
emissions [6] and that diesel with higher carbon numbers contributes to emissions of high
particulate matters, high sulphur dioxide and high poly aromatic hydrocarbons [5]. Thus,
need for the kind of serious attention being witness in the search for economically viable
and environmental friendly renewable fuels like biodiesel.
Biodiesel has been reported to have offered reduced exhaust emissions, improved
biodegradability, reduced toxicity and higher cetane rating which can improve performance
and clean up emissions [7]. More so, vegetable oil has good resource for the production of
biodiesel through transesterification of different types like canola, rapeseed, soybean oil,
rapeseed etc [8]. Interesting results have been reported on the production of biodiesel
through transesterification of different kinds of vegetable oil from different parts of the
world, such include soybean (United State), rapeseed (Europe), oil palm (South-East Asia),
jatropha curcus and rice bran oil (India) [9-13]. Besides, esters from vegetable oils have been
reported as the best substitutes for diesel because they do not demand any modification in
the diesel engine and have a high energetic yield [14]. Fossil fuels dependent countries like
Energy Conservation 198
Nigeria have commenced initiation of policies aimed at re-directing the nations major
energy sources from the finite crude oil to renewable sources. Interestingly, Nigeria is
endowed with different renewable energy resources to support the implementation of such
policies as reported by [5, 15]. Literature have shown that vegetable oils are one of the
significant renewable feedstock that can provides secure, abundant, cost effective and clean
source of energy for developing nations like Nigeria. Common vegetable oil in the country
include palm oil, palm kernel oil (PKO), groundnut oil, cottonseed and soybean [5].
Considerable works have been reported in print on biodiesel production from vegetable oils
but limited studies were found for vegetable oils common in Nigeria. As at year 2000,
limited studies were reported in the literature on production and testing of biodiesel from
Nigerian Lauric oils [5]. Recent development only shows some improvement on the
exploitation of Nigeria vegetable oils as resources for biodiesel production, such include
transesterification of palm kernel oil [5, 16], transesterification of groundnut oil [17-19]. With
increasing attention on the use of these oils for biodiesel production, the present study
focused more on the optimization of biodiesel production from refined groundnut oil
relative to the effects of the major reaction parameters. Groundnut oil has been reported to
be among the most consumed vegetable oil and the 13
th
most important food crop in the
world. It is also known to contain a high percentage of unsaturated fatty acid namely oleic
and linoleic acid [20] and low free fatty acid value [21].Groundnut seed contain high quality
edible oils, protein, and carbohydrate. Globally, 50% of groundnut produced is used for oil
extraction, 37% for confectionary use and 12% for seed purpose. The fat in the oil is
approximately 50% monounsaturated, and 30% polyunsaturated [22]. In comparison,
groundnut oil has been reported of having capacity to produce approximately 123 gallons of
biodiesel per acre while soybeans yield only 50 gallons [23]. This research work is therefore
aimed at optimizing the production of biodiesel from groundnut oil due to its cheapness and
availability. This aim can be achieved through the realization of the following objectives;
i. Characterization of the commercially obtained refined groundnut oil by testing for
properties like Specific gravity (or density), flash point, kinematic viscosity, acid value,
iodine value, sulphur content, moisture or water content etc. Comparison of the results
with literature values.
ii. Conversion of the groundnut oil into biodiesel through alkali-based transesterification
with methanol using sodium hydroxide (NaOH) as catalyst.
iii. Detailed characterization of the properties of biodiesel produced and comparison of the
experimental results obtained with available standards.
iv. Investigation of the effects of temperature, reaction time, catalyst concentration, and
mass ratio of methanol to groundnut oil on production yield of the biodiesel.
1.1. First biodisel
Walton J., in 1938 recommended that to get the utmost value from vegetable oils as fuel, it
is academically necessary to split off the triglycerides and to run on the residual fatty acid.
Practical experiments have not yet been carried out with this; the problems are likely to be
much more difficult when using free fatty acids than when using the oils straight from the
Production and Characterization of Biofuel from Refined Groundnut Oil 199
crushing mill. It is obvious that the glycerides have no fuel value and in addition are likely
to cause an excess of carbon in comparison with gas oil. Waltons statement pointed in the
direction of what is now termed biodiesel by recommending the elimination of glycerol
from the fuel, although esters was not mentioned. In this connection, some remarkable work
performed in Belgium and its former colony, the Belgian Congo (known after its
independence for a long time as Zaire), deserves more recognition than it has received. It
appears that Belgian patent 422,877, granted on Aug. 31, 1937 to Chavanne G. (University of
Brussels, Belgium), constitutes the first report on what is today known as biodiesel. It
describes the use of ethyl esters of palm oil (although other oils and methyl esters was
mentioned) as diesel fuel. These esters were obtained by acid-catalyzed transesterification of
the oil (base catalysis is now more common). This work was of particular interest as it was
related to an extensive report published in 1942 on the production and use of palm oil ethyl
ester as fuel and the work described the first test of an urban bus operating on biodiesel. A
bus fueled with palm oil ethyl ester served the commercial passenger line between Brussels
and Louvain (Leuven) in the summer of 1938. The performance of the bus operating on that
fuel was reportedly satisfactory. It was noted that the viscosity difference between the esters
and conventional diesel fuel was considerably less than that between the parent oil and
conventional diesel fuel [24]. The patent also pointed out that the esters are miscible with
other fuels and the work also discussed the cetane number (CN) testing of a biodiesel fuel.
In the report, the CN of palm oil ethyl ester was reported as ~83 (relative to a high-quality
standard with CN 70.5, a low-quality standard of CN 18, and diesel fuels with CN of 50 and
57.5). Thus, the reported results agree with modern work reporting relatively high CN for
such biodiesel fuels. A later paper by another author reported the auto-ignition temperature
of various alkyl esters of palm oil fatty acids [25]. In more recent times, the use of methyl
esters of sunflower oil to reduce the viscosity of vegetable oil was reported at several
technical conferences in 1980 and 1981 [26] and marks the beginning of the rediscovery and
eventual commercialization of biodiesel. In a similar manner, palm oil was often considered
as a source of diesel fuel in the historic studies [27]. Although, the diversity of oils and fats
as sources of diesel fuel had been investigated and reported, however, an important aspect
again today and striving for energy independence were reflected in other historic
investigations [28]. Vegetable oils were also used as emergency fuels and for other purposes
during World War II. [29]. For example, Brazil prohibited the export of cottonseed oil so that
it could be substituted for imported diesel fuel. Reduced imports of liquid fuel were also
reported in Argentina, necessitating the commercial exploitation of vegetable oils [28].
China produced diesel fuel, lubricating oils, gasoline and kerosene, the latter two by a
cracking process and other vegetable oils. However, the exigencies of the war caused hasty
installation of cracking plants based on fragmentary data. Researchers in India, prompted
by the events of World War II, extended their investigations on 10 vegetable oils for
development as domestic fuels. Work on vegetable oils as diesel fuel ceased in India when
petroleum-based diesel fuel again became easily available at low cost [29]. The Japanese
battleship Yamato reportedly used edible refined soya bean oil as bunker fuel [30]. Concerns
about the rising use of petroleum fuels and the possibility of resultant fuel shortages in the
United States in the years after World War II played a role in inspiring a dual fuel project
at the Ohio State University, during which cottonseed oil, corn oil and blends with
Energy Conservation 200
conventional diesel fuel were investigated [28]. In modern times, biodiesel is derived or has
been reported to be producible from many different sources, including vegetable oils,
animal fats, used frying oils and even soap stock [31]. Generally, factors such as geography,
climate, and economics determine which vegetable oil is of greatest interest for potential use
in biodiesel fuels [32]. Thus, in the United States, soybean oil is considered to be a prime
feedstock; in Europe, it is rapeseed (canola) oil, and in tropical countries, it is palm oil. As
noted above, different feed stocks were investigated in the historic times. These included
palm oil, soybean oil, cottonseed oil, groudnut oil, castor oil and a few less common oils
such as babassu and crude raisin seed oil; non-vegetable sources such as industrial tallow
and even fish oils were also investigated [26]. Walton, (1938) summarized results on 20
vegetable oils (castor, grapeseed, maize, camelina, pumpkinseed, beechnut, rapeseed, lupin,
pea, poppyseed, groudnut, hemp, linseed, chestnut, sunflower seed, palm, olive, soybean,
cottonseed, and shea-butter). He also pointed out that at the moment the source of supply
of fuels is in a few hands, the operator has little or no control over prices or qualities and it
seems unfortunate that at this date, as with the petrol engine, the engine has to be designed
to suit the fuel whereas strictly speaking, the reverse should be the case, that is, obtaining
the fuel and refining it to meet the design of an ideal engine [26]. Although, environmental
aspects played virtually no role in promoting the use of vegetable oils as fuel in historic
times and no emissions studies were conducted, it is still worthwhile to note some allusions
to this subject from that time; (i) In case further development of vegetable oils as fuel
proves practicable, it will simplify the fuel problems of many tropical localities remote from
mineral fuel and where the use of wood entails much extra labor and other difficulties
connected with the various heating capacities of the woods use, to say nothing of the risk of
indiscriminate deforestation [33]. (ii) It might be advisable to mention, at this juncture, that,
owing to the altered combustion characteristics, the exhaust with all these oils is invariably
quite clean and the characteristic diesel knock is virtually eliminated [26]. (iii) Observations
by other authors included: invisible or slightly smoky exhausts when running an engine
on palm oil [34]; clearer exhaust gases; in the case of use of fish oils as diesel fuels, the exhaust
was described as colorless and practically odorless [35]. These visual observations of yesterday
have been confirmed in modern times for biodiesel fuel. Numerous recent studies showed that
biodiesel fuel reduces most exhaust emissions [28, 31].
1.2. Production and processing of biodiesel
The production process of biodiesl involve combination of Alcohol, oil and catalyst in an
agitated reactor, approx. at 60C during 1hr. Smaller plants often use batch mode reactors,
but larger plants use continuous flows processes involving continuous stirred-tank reactors
or plug flow reactors. Biodiesel as a renewable source of energy can be produced from
different sources such as lipids, animal fats, vegetable oils and waste vegetable oils (Table 2).
It has been reported that the production of biodiesel feedstock is sensitive [27, 36-37]. For
instance, the cost of biodiesel can be estimated based on assumption regarding production
volume, feedstock and chemical technology, hence feedstock cost comprises a substantial
portion of overall biodiesel cost [38, 39]. Production of biodiesel from fats and oils is
motivated by the fact that fat and oils contain a glycerol molecule bonded to three fatty acid
Production and Characterization of Biofuel from Refined Groundnut Oil 201
chains, this structure is called a triglyceride and it is the major component of the oil. In
general, biodiesel feedstock can be categorized into three groups: Pure vegetable oils (edible
or non-edible), animal fats and waste cooking oils. Pure vegetable oil is also utilized for the
production of biodiesel due to the fact that the oil composition from vegetable crops is pure
[40]. Most liquid plant oils are composed predominantly 18-carbon fatty acids. Oils, which
tend to be a liquid at room temperature, tend to have more double-bonds than fats. The
major oils of this group are: rapeseed oil (canola), soybean oil, palm oil, sunflower oil, corn
oil, groundnut (groudnut) oil, coconut oil, safflower oil, linseed oil, hemp, microalgae oil,
Jatropha curcas and Pongamia pinnata [41]. Fats, which tend to be solid at room temperature,
can also be used as a feedstock for the production of biodiesel. Fats have shorter carbon fatty
acids and tend to have fewer double bonds than oils. These include: sheep tallow, yellow
grease, beef, and poultry oil etc. Also used in the production of biodiesel is the waste cooking
oils. These are also denominated in literatures as waste fried oils (WFO). It include: used
rapeseed oil, used sunflower oil, used soybean oil, used cottonseed oil, used olive oil. The use
of waste oil for the production of biodiesel has been identified as economical method, due to
the availability of waste cooking oil, however processing and gathering of the waste cooking
oil militate against its adoption. Commercial availability of biodiesel is therefore influence by
the feedstock availability, which can be achieved in Nigeria through groundnut oil with
production rate of 200 000 metric tonne per year.
S/N Chemical Name Fatty acid Methyl Ester
1 Chemical Formula Range C14-C24 methyl esters
2 Kinematic Viscosity Range 3,3- 5,2
3 Density Range 860-894
4 Boiling point Range (K)
Flash Point Range (K)
>475
430-455
5 Distillation Range (K) 470-600
6 Vapor Pressure (mmHg at 295K) <5
7 Solubility in water Insoluble in water
8 Physical appearance Light to dark yellow
transparent liquid
Table 1. Physical Biodiesel Properties (Shay, 1993)
1.3. Availability and properties of groudnut oil
Groudnut oil (arachis oil) is an organic material oil derived from groudnuts and it has been
noted to have the aroma and taste of its parent legume. It is often used in Chinese, South
Asian and Southeast Asian cuisine as much as olive oil is used in the Mediterranean.
Groudnut oil is appreciated for its high smoke point relative to many other cooking oils. Its
major component fatty acids are oleic acid (46.8% as olein), linoleic acid (33.4% as linolein),
and palmitic acid (10.0% as palmitin). The oil also contains some stearic acid, arachidic acid,
arachidonic acid, behenic acid, lignoceric acid and other fatty acid [28, 29]. Vegetable oils are
Energy Conservation 202
widely consumed domestically in Nigeria. It is used primarily as a cooking and salad oil.
Studies have shown that groundnut oil contains much potassium than sodium and is a good
source for calcium, phosphorus and magnesium. It also contains thiamin, vitamin E,
selenium, zinc and arginine [42]. Findings have demonstrated that diets high in groudnut oil
are as effective as olive oil in preventing heart disease and are heart healthy than very low
fat diets [42]. Groudnut oil is of high quality and can withstand higher temperatures
without burning or breaking down, has neutral flavour and odour, does not absorb odour
from other foods and all these properties thus makes it the most preferred oil in Northern
Nigeria [32]. The nutritional values of the groudnut oil are however affected by the method
and period of storage, which consequently affect the acceptability of these oils. In Northern
Nigeria, women usually do extraction of groudnut oil locally. The women extract the oil to
generate substantial income to support their domestic needs with little or no consideration
given to groudnut species or the physicochemical properties of the oil. Most women rely on
availability rather than quality. Groudnut is mainly grown in the Northern part of Nigeria and
the oil is readily available in all parts of Nigeria in large quantities. This is because it has been
reported that Nigeria possesses land area of 923,768 km
2
arable land constituting about 56%
and vegetation ranging from the Sahel savanna in the extreme North to swamp forest in the
south [32]. Therefore most parts of Nigeria are suitable for biofuel crop cultivation. Although
an edible oil, its use as a potential feedstock for biodiesel production may not likely compete
with other crops grown for food and commercial cooking oil products. Nigerian is ranked 3
rd
in the world for the production of groundnut oil as shown in Table 3 (USDA, 2009)[43]. The
annual production of groundnut in Nigeria is shown in Figure 1. The reduction in the
production of groundnut oil between the year 1976 and 1994 can be attributed to the diversion
of Nigerian economy from agricultural oil exploitation economy due to discovery of oil in
Nigeria. The recent interest (from 1999 till date) in the production of groundnut can be
attributed to the Nigerian government commitment to the production of alternative renewable
energy sources. Biodiesel has been identified as the alternative energy in the country with
groundnut oil as the perfect feedstock for its production without affecting the oil supply for
consumption purpose.
S/No Vegetable oil Production
(billion/year)
Animal Fats Production
(pounds/year)
1. Soybean 18.340 Edible tallow 1.625
2. Groudnut 0.220 Inedible
tallow
3.859
3. Cotton seed 1.000 Lard and
Grease
1.306
4. Sunflower 1.010 Yellow Grease 2.633
5. Corn 2.420 Poultry Fat 2.215
6. Others 0.669
TOTAL 23.659 TOTAL 1.638
Table 2. Annual Oil Productions of Some Biodiesel Sources [44]
Production and Characterization of Biofuel from Refined Groundnut Oil 203
Figure 1. Nigerias Groundnut (Peanut) Oil Production per Year (United States Department of
Agriculture, 2011)
S/No Country Production
Million metric tons
1. Peoples Republic of China 14.30
2. India 6.25
3. United States 2.34
4. Nigeria 1.55
5. Indonesia 1.25
6. Myanmar 1.00
7. Sudan 0.85
8. Senegal 0.71
9. Argentina 0.58
10. Vietnam 0.50
11. TOTAL 34.43
Table 3. Worlds Top Ten Producers of Groundnut (Groudnut) [43].
It has been estimated that in the year 2000, approximately 34 million Mt of groundnuts were
produced world wide of which 15 million Mt were produced in China, 6 million Mt in India, 2
Energy Conservation 204
million Mt in Nigeria, 1.5 million Mt in United States of America and the rest mostly in other
countries [45]. Groundnuts are important component of Nigerian diet and about 5 percent of
the estimated 58.9 g of crude protein available per head per day is contributed by groundnut
[45]. In most of the developing countries it provides high-quality cooking oil and is an
important source of protein for both human and animal diet and also provides much needed
foreign exchange by exporting the kernels and cake. Hence, the utilization of groundnut oil for
biodiesel production without affecting the supply of the vegetable oil for consumption.
2. Material and methodology
The feedstock used in this work for the production of biodiesel is refined groundnut oil
produced by Grand Cereals Mill Zawan, Plateau state, Nigeria. This product was purchased
at a local super market in Minna Niger State, Nigeria. The entire chemicals used in this
study are of analytical grade (98-99.5%). They include Carbon tetra chloride (Analar, BDH),
Wijs solution (Mixture of glacial acetate, iodine trichloride and carbon tetralchloride)
(Hopkins and Williams, London), potasium hydroxide solution (Analar, BDH), potassium
hydroxide pellet (Burgoyne & co, India), petroleum ether (Analar, BDH), potassium iodide
solution (M&B, England), sodium thisosulphate (M&B, England), hydrochloric acid (Analar,
BDH) and potassium iodide pellet (M&B, England). The equipments used are pH meter,
distillation apparatus, viscometer, thermostatic hot plate, sulphur in oil analyzer, magnetic
stirrer, digital weighing balance, thermometer, petri dish, pippete, separating funnel, burete,
oil test centrifuge, pycometer bottles, Abbe refractometer, flash point tester, oven and
aneline point teseter.
Production of biodiesel from groundnut oil was carried out in accordance to the experimental
procedure reported by Hill (2002) [45]. Methoxide was first prepared in a suitable container by
dissolving sodium hydroxide in methanol. This typically consists of 50% methanol by volume
of oil and 0.25 grams sodium hydroxide for lower limit and 0.50grams sodium hydroxide for
upper limit mixed together well so that the sodium hydroxide is completely dissolved in the
methanol in the ratio of 1:4 for lower limit and 1:6 for upper limit respectively.
Transesterification reactions were carried out in a reaction vessel (250ml flask). The reactor
was filled with 50g refined groundnut oil sample and preheated to the selected reaction
temperature (40
0
C and 60
0
C); the methoxide solution was then added on top of the oil. The
mixture was agitated vigorously for about 30 seconds and then placed on a magnetic stirrer for
stirring to continue for the reaction time (45 and 90 minutes respectively). The
transesterification was carried out on the hot plate to keep the reaction temperature constant,
after reaction time was reached, the reaction mixture was then poured into a separating funnel
and allowed to settle gravitationally for about 8-20hrs. After settling, a lighter colored biodiesel
on top of a layer of darker glycerin was observed. The bottom layer (glycerol) was drained off
and the top layer (methyl esters) was collected in a clean beaker.
Characterization of the feedstock (refined groundnut oil) is very important for proper
understanding of its chemical composition, as well as physico-chemical properties to ease
comparison with standard and possibly establish the level of purity of the material relative
Production and Characterization of Biofuel from Refined Groundnut Oil 205
to using it for biodiesel production. Properties of the feedstock tested for are the specific
gravity (or density), flash point, kinematic viscosity, acid value, iodine value, sulphur
content, moisture content, free fatty acid and acid value. Determination of these properties
was carried out using the experimental description reported by Onwuka (2005) [46]. Next to
the prelimenary production of biodiesel from groudnut oil was the process optimization by
investigating the effects of various parameters on the yield of biodiesel from groudnut oil.
Effects of operating parameters such as temperature, time of reaction, and catalyst
concentration as well as oil-methanol mass (or mole) ratio were investigated. A 2
4
factorial
experimental design was used to carry out the study. A 2
4
factorial experimental design was
used to determine the optimum conditions for biodiesel production from groundnut oil,
four variables were studied at both high and low levels. The expected response is biodiesel
(methyl ester) yield. The low level of methanol: oil mass ratio was 6:1 and the high level was
4:1. The low level of catalyst concentration chosen was 0.5% and the high level was 1.0%
NaOH catalyst by weight of groundnut oil. The low level of temperature was chosen as 40
C and the high level was chosen at 60 C, which was determined by the boiling point of
methanol. The reaction time chosen for the lower level was 45 minutes and 90 minutes for
the higher level. Table 4 shows the experimental matrix for the 2
4
factominrial designs
(4factors, each run at two levels). The biodiesel produced was then analyzed to determine
the specific gravity, flash point, cloud point, kinematic viscosity, pour point, centane
number, acid value, bottom water and sediment, sulphur content, ash content and
distillation characteristics. All experimental analysis were conducted in triplicate and the
results reported are the average values with average deviation of 0.0015
Run Temperature
(
o
C)
Methanol : oil ratio
(wt/wt)
Catalyst Conc.
(wt %)
Reaction
time (min)
1 40 1:4 0.5 45
2 60 1:4 0.5 45
3 40 1:6 0.5 45
4 60 1:6 0.5 45
5 40 1:4 1.0 45
6 60 1:4 1.0 45
7 40 1:6 1.0 45
8 60 1:6 1.0 45
9 40 1:4 0.5 90
10 60 1:4 0.5 90
11 40 1:6 0.5 90
12 60 1:6 0.5 90
13 40 1:4 1.0 90
14 60 1:4 1.0 90
15 40 1:6 1.0 90
16 60 1:6 1.0 90
Table 4. 2
4
Factorial design
Energy Conservation 206
3. Results and discussion of results
Refined groundnut oil that was used as the feedstock for the production of biodiesel was
characterized to determine the necessary properties that are very essential to the quality and
quantity of the final product. Table 5 summarized the results obtained on the qualities of the
refined groundnut. Presented in Table 6 is the results obtained on the influence of the
operating parameters on the yield of biodiesel, while Table 7 represent the properties of the
biodiesel produced from refined groundnut oil. Also presented is the statistical analysis of
the results obtained to illustrate the effect of each of the operating parameters on the yield of
the biodiesel from the refined groundnut oil.
Table 5 summarized the results of characterization carried out on the sample of refined
groundnut oil used and the results were compared with standard and available literature.
The main properties determined include saponification value, iodine value, acid value, free
fatty acid, peroxide value, refractive index, kinematic viscosity, pH, unsaponifiable matter
and the moisture content, results obtained are hereby presented.
The saponification value of as reported by Al-Zahrani (2005) [48] is a measure of the
tendency of oil to form soap during transesterification reaction (i.e. define as the number in
milligram (mg) of KOH required to saponified 1g of the sample fat).The saponification value
obtained for sample of refined groundnut oil was 186.53, which is lower compared to 188-
195 recommended by AOCS standard(1998) [46], but higher than 148.67 reported for the
variety used by Ibeto et al. (2011) [47].The high saponification values indicate the presence of
high percentage of fatty acids which might lead to soap formation and hence low biodiesel
yield [48]. Unsaponifiable matter are those substances frequently found dissolved in fatty
acids and drying oils which cannot be saponified by caustic treatment, but which are soluble
in normal fat solvents. The unsaponifiable value for the oil sample used oil was 0.29% which
is very reasonable compared to 1% maximum recommended by AOCS standards as
presented in Table 5. Iodine Value (IV) is a value of the amount of iodine, measured in
grams, absorbed by 100 grams of given oil. The iodine value is expressed in grams of iodine
for the amount of halogens linked with 100g test sample, and is used as degree of
unsaturated bond of fats and oils. Iodine values are used to classify oils as either drying oil
(>130), semi-drying oil (115-130) and non-drying oil (<115) (Othmer, 2011) [49]. The oil used
in the present study has iodine value of 94.16gI2/100g, although higher than
89.46gI2/100greported for the groundnut oil sample used by Ibeto et al. (2011) [47] but falls
within the 84-100gI2/100g range recommended by AOCS standard of 1998. Based on this
value, the present oil in use can be classified as non-drying oil. Also measured is the acid
value (AV) of the oil which is an important indicator of vegetable oil quality. Vegetable oils
with high acid value are classified as inedible while those with low acid value are classified
as edible oils [48]. The obtained acid value for the present oil sample was 2.174mgKOH/g, a
value that falls within 0.72-3.0mgKOH/g reported in the AOCS standard (1998) [46] but
lower when compare to 2.61mgKOH/g obtained by Ibeto et al (2011) [47]. However, both
reported values of the present study and that of Ibeto et al. (2011) [47] indicated the oil
Production and Characterization of Biofuel from Refined Groundnut Oil 207
samples are edible type. Results as presented in Table 5 also indicate that the Free Fatty Acid
(FFA) value of the refined groundnut oil sample was 0.05%, and was found to fall within the
AOCS standard having its FFA value as <1% (AOCS, 1998) . Literature also revealed that for
groundnut oil to be fit for biodiesel production its free fatty acid content should be <2%, this
is to enable efficient conversion of the oil into biodiesel (Anggraini and Wiederwertung,
1999) [50]. Ibeto et al (2011) obtained a free fatty acid value of 1.31mgKOH/g, translating to
0.065%which was a little bit higher than 0.05% reported in this study.
S/No Properties Unit Experimental
values
AOCS
Standard value
(1998)
Ibeto et
al.,
(2011)
1. Specific gravity (S.G) - 0.91 0.910-0.915 0.93
2. Kinematic Viscosity at
25
o
C
mm
2
sec
-1
38.00 - 32.66
3. Saponification value (S.V) mgKOH/g 186.53 188-195 148.67
4. Moisture content % 0.05 - 0.09
5. Iodine value (I.V) gI2/100g 94.16 84-100 89.46
6. Unsaponifiable matter % 0.29 1% max -
7. pH 5.56 - -
8. Refractive index (R.I) at
25
0
C
- 1.467 1.467-1.470 1.463
9. Acid value (A.V) mgKOH/g 2.174 0.72-3.0 2.61
10. Free fatty acid (FFA) % 0.05 <1% 1.31
11. Peroxide value mEq/kg 0.059 - 22.25
Table 5. Measured Physiochemical Properties of Refined groundnut oil.
Kinematic viscosity refers to the thickness of the oil and its value is meaningless unless
accompanied by the temperature at which it is determined. The purpose of transesterified
vegetable oils and animal fats into alkyl esters (biodiesel) is to reduce the kinematic viscosity
because high viscosity tends to form larger droplets on injection which can cause poor
combustion, increased exhaust smoke and emissions. Hence, kinematic viscosity is key
factor in checking suitability of a feedstock for the production of biodiesel. Result obtained
as presented in Table 5 shown that the kinematic viscosity of the refined groundnut utilized
in this study for the production of biodiesel is 38mm
2
/sec at 25
0
C, which is much higher
compared to 32.66 mm
2
/sec obtained by Ibeto et al (2011). While the specific gravity of the
refined groundnut oil was found to be 0.91, which falls within the range of AOCS
specification (0.910-0.915) and lower than 0.93 reported by Ibeto et al. (2011). The peroxide
value obtained for the refined groundnut oil was 0.059mEq/kg which was very low
compared to 22.25 mEq/kg obtained by Ibeto et al (2011). The value obtained is considered
reasonable, because literature suggest that the peroxide values of fresh oils should be less
Energy Conservation 208
than 10 millequivalents /kg, peroxide values between 30 and 40 millequivalents/kg will
results into rancidity of the oil. The moisture content in the oil sample as shown in Table 5
was found to be 0.05% and much lower compared to 0.09%reported for the oil sample used
by Ibeto et al (2011).The 0.05% value obtained agreed with the value recommended by
ASTM (D 6571) and falls within the <3% moisture content suggested for all raw materials to
be used in the production of biodiesel (Freedman et al., 1984). It has been reported that
moisture content greater than <3% will decrease the efficiency of the transesterification
reaction due to possibility deactivation of catalyst active sites and soap formation
(Freedman et al., 1984). The result obtained on the refractive index of the oil sample at 25
0
C
was 1.467 which was within the recommended AOCS standard index of 1.467-1.470 and also
compared well with 1.463 reported by Ibeto et al. (2011). It can be inferred from the various
analysis conducted on the refined groundnut oil sample that the oil sample compare
favorably with the standard and literature value, hence the oil sample utilized in this study
should produced biodiesel with high yield and quality.
The effect of reaction parameters on the yield of biodiesel produced from refined groundnut
oil was investigated using a 2
4
factorial design. Reaction parameters considered include
mole ratio of methanol to refined groundnut oil, reaction temperature, catalyst
concentration and reaction time. Each of these parameters was considered at two specified
levels and the summary of results obtained was presented in Table 6. As shown in Table 6,
the best biodiesel yield of 99% was obtained under the optimal conditions of 1:6 (oil to
methanol) molar ratio, 0.5% catalyst concentration at 40
o
C and for a reaction time of 90
minutes. This value was better than 88% and 79% reported by Galadima et al.(2008) and
Ibeto et al .(2011) respectively. The better ester production yield obtained could be attributed
to different reaction parameters used in conducting the experiment, different alcohol and
alkali catalyst and possible variation in the specie of groundnut oil used which is attested to
the values obtained for the characterization of the oil (Table 5).
One of the most important parameters that affects biodiesel yield is the oil: alcohol ratio (in
this case refined groundnut oil to methanol) mole ratio [51]. In order to evaluate its effect on
biodiesel yield, transesterification was conducted at two different molar ratios of 1:4 and 1:6.
Though, the stoichiometric ratio for transesterification requires one (1) mole of triglyceride
and three (3) moles of alcohol to yield three moles of fatty acid alkyl esters and one mole of
glycerol. However, transesterification is an equilibrium reaction in which a large excess of
alcohol is required to drive the reaction to the product side. In this work, two levels of
Groundnut Oil to MeOH molar ratio were used, 1:4 for the low level and 1:6 for the high
level. The yields ranging from 94-99% were obtained at a molar ratio of 1:6. It can be seen
from Figure 2 that the biodiesel yield increased for both 0.5 wt% and 1.0 wt% catalyst
concentration as the molar ratio was increased from 1:4 to 1:6 i.e. from 96 to 99% for 0.5wt%
and from 80 to 92% for 1.0wt% catalyst weight respectively. While temperature and time
were constant and this achieved experimental result is in agreement with Freedman et al
(1984) [52]. Since transesterification is an equilibrium process, lower oil to methanol molar
ratio may result in an incomplete transesterification and thus increasing the molar ratio
which will shift the reaction to the ester formation direction. However when the molar ratio
Production and Characterization of Biofuel from Refined Groundnut Oil 209
Run Temperature Oil:
Methanol
mole
ratio
Catalyst
weight
(wt %)
Reaction
time
Production
yield (wt %)
Methyl ester
concentration
(wt %)
Methyl
ester
yield
(wt %)
1 40 1:4 0.50 45 96 97.92 94
2 60 1:4 0.50 45 90 80.00 72
3 40 1:6 0.50 45 96 97.92 94
4 60 1:6 0.50 45 98 97.96 96
5 40 1:4 1.00 45 94 97.87 92
6 60 1:4 1.00 45 76 92.11 70
7 40 1:6 1.00 45 96 93.75 90
8 60 1:6 1.00 45 96 95.83 92
9 40 1:4 0.50 90 100 96.00 96
10 60 1:4 0.50 90 98 97.96 96
11 40 1:6 0.50 90 101 98.02 99
12 60 1:6 0.50 90 98 97.96 96
13 40 1:4 1.00 90 82 97.56 80
14 60 1:4 1.00 90 80 95.00 76
15 40 1:6 1.00 90 94 97.87 92
16 60 1:6 1.00 90 92 97.83 90
Table 6. Biodiesel Yield at Different Conditions
Figure 2. Effect of methanol to oil ratio on methyl ester yield at 40
0
C and 90 minutes reaction time.
is set too high, the excessive alcohol may favor conversion of triglycerides to diglycerides
and then monoglycerides and a slight recombination of esters and glycerol to
0
20
40
60
80
100
120
1;4 1;6
m
e
t
h
y
l
e
s
t
e
r
y
i
e
l
d
methanol to oil ratio
0.5wt%
1.0wt%
Energy Conservation 210
monoglycerides because their concentrations keep increasing during the course of the
reaction. The detailed analysis of the results obtained on the effects of various parameters on
the yield of biodiesel from groudnut oil are presented below.
The rate of reaction and biodiesel yield can be affected by reaction temperature, Anitha and
Dawn, (2010) in their work varied the temperature between 40-65
0
C and concluded that the
primary advantage of a high temperature is shorter reaction time. Transesterification can
occur at different temperatures depending on the oil used. Several researchers found that
the temperature increase influences the reaction in a positive manner (Ma and Hanna, 1990;
Freedman et al., 1984; Canakci and Van Gerpen, 1999). Though, it has been reported that the
best temperature for the reaction is 60
o
C but depending on the type of catalyst, different
temperatures will give different degrees of conversion. In this work, the two levels of
temperature used were 40
o
C for the low level and 60
o
C for the high level. The best yields
were obtained at the low temperature of 40
o
C as presented in Figure 3. This pattern of
results can be attribute to the fact at a high temperature of 60
o
C most of the alcohol in the
biodiesel would evaporate during transesterification reaction leading to a lower yield
Anitha and Dawn (2010), also confirmed this. The figure also confirmed that as the
temperature increase from 40
0
C to 60
0
C the methyl ester yield decreased from 94 to 92% for
0.5wt % catalyst weight and from 92 to 70%for 1.0wt% catalyst weight respectively.
Analysis of result obtained as presented in Table 5 shows that increase in time does not
implies increase in yield as suggested by Yusuf and Sirajo (2009). For instance, at 40
o
C using
1:4 mole ratios with 1wt% catalyst for 45min gave a yield of 92% while the yield decreased
to 80% at the same condition but with 90min reaction time. In this study, two levels of
reaction time were used i.e. 45 minutes for the low level and 90 minutes for the high level.
The optimum yield (99%) was achieved at 90minutes and this observation is in agreement
with Freedmans work and Ahmad et al., (2009). Figure 4 which also depict the effect of time
on the methyl ester yield indicate that the maximum methyl ester yield at 45minutes was
Figure 3. Effect of reaction temperature on methyl ester yield at 40
0
C at 45 minutes reaction time.
0
10
20
30
40
50
60
70
80
90
100
40 60
m
e
t
h
y
l
e
s
t
e
r
y
i
e
l
d
reaction temperature
0.5wt%
1.0wt%
Production and Characterization of Biofuel from Refined Groundnut Oil 211
Figure 4. Effect of reaction time on methyl Ester Yield at 40
0
C using 1:6 methanols to oil ratio.
96% which is less than the value obtained at 90 minutes (99%) at same reaction conditions.
This indicates that there is increase in biodiesel yield as reaction time increases although this
could be as a result of varying other variables too.
Also investigated is the effect of catalyst on the yield of the biodiesel from grudnut oil. It has
been reported that as the catalyst concentration increases, the conversion of triglyceride and
the yield of biodiesel also increase. This phenomenon was attributed to an increase in the
availability and number of catalytically active sites (Anitha and Dawn, 2010). This is because
an insufficient amount of catalysts will result in an incomplete conversion of the
triglycerides into the fatty acid esters (Anitha and Dawn, 2010). Two levels of catalyst
concentration (NaOH) were used in this work, 0.5wt% for the lower and 1.0wt% for the
higher level. From the obtained experimental result shown in Table 6 and Figure 5, it was
observed that the best yield which was 99% was obtained at 0.5wt% NaOH, but at 40
0
C, 1:6
and a reaction time of 90minutes. Although the smaller the catalyst concentration, the lower
the yield due to insufficient amount of catalyst to catalyze the reaction to a completion stage
but this result was achieved due to the excess of alcohol used in this condition. It can be seen
from Figure 5 also that the methyl ester yield is higher at catalyst concentration of 0.5 wt%
than at 1.0wt%. Also, it was observed that at conditions other than the optimal conditions of
1:6 molar ratio, 60
o
C and 90 minutes reaction time, 1.0 wt% catalyst weight gave a lower
yield in most run than the 0.5 wt% for same conditions. Most researchers said that an
increase in catalyst concentration increases the methyl ester yield (Anitha and Dawn, 2010;
Yusuf and Sirajo, 2009) but from this research, higher catalyst concentration gave lower
yield, as shown in Figure 5.
Biodiesel produced from refined groundnut oil using alkali catalyzed transesterification
process with sodium hydroxide (NaOH) as catalyst and methanol as alcohol was
characterized to determine its suitability as alternative to petrol diesel. Results obtained on
the various analysis conducted are presented in Table 7.
84
86
88
90
92
94
96
98
100
45 90
M
e
t
h
y
l
e
s
t
e
r
y
i
e
l
d
Reaction time
0.5wt%
1.0wt%
Energy Conservation 212
Figure 5. Effect of Catalyst Concentration on Ethyl Ester Yield.
Results as presented in Table 7 indicate that the kinematic viscosity of the biodiesel
produced was determined as 5.86 mm
2
/ s, a value that falls within the range of 1.9-6.0mm
2
/s
recommended by ASTM (DS 6751) and a little higher than 5.16mm
2
/s reported by Ibeto et al.
(2011). However, the value obtained shows that the transesterification reaction has
successfully reduced the viscosity of oil from38mm
2
/s to 5.86 mm
2
/s and as such increases its
tendency to flow. Since kinematic viscosity described the resistance of a fluid to flow under
gravity and it is important in determining optimum handling, storage, and operational
conditions. High viscosity can cause fuel flow problems and lead to stall out or fuel pump
failure [54]. Also presented in Table 7 is the results obtained for the bottom sediment and
water content of the biofuel produced. Presence of water and sediment in biodiesel beyond
standard limit will results in poor ignition, filter clogging, and fuel pump problems,
sediment in storage tanks can obstruct the flow of fuel from the tank to a combustor and
presence of water in middle distillate fuels can cause corrosion and growth of
microorganisms. According to ASTM standard, a maximum water content of 0.05%vol fuels
is acceptable, while the biodiesel produced contain trace quantity of water and sediment.
This is similar to the results reported by Ibeto et al. (2011) and better than 0.02% water and
sediment reported by Galadima et al. (2008) [53]. This result gave an indication that the
biodiesel is clean and properly dried. Sulphur content of the biodiesel produced was
measured and the result obtained is as shown in Table 7. Pure biodiesel (B100) is expected to
contain very low quantities of sulfur in order to retain its traditional name of sulphur-free
fuel. The sulphur content of the biodiesel produced was found to be 0.025 wt% (Table 7) and
this is low when compared to ASTM maximum limit of 0.050wt%. It can be inferred that the
fuel produced is Sulphur free. Also presented in Table 7 is the distillation characteristic of
the produced biodiesel, though for a pure substance the boiling point is a single temperature
value. However, when a mixture of hydrocarbons exists in diesel fuel there is a range of
boiling points for the different constituent chemical specie, the boiling point of the biodiesel
0
20
40
60
80
100
120
1;4 1;6
m
e
t
h
y
l
e
s
t
e
r
y
i
e
l
d
methanol to oil ratio
0.5wt%
1.0wt%
Production and Characterization of Biofuel from Refined Groundnut Oil 213
Properties Units Experimenta
l values
ASTM
standard
biodiesel
(ASTM D 6751)
ASTM
standard
Petrol-diesel
(ASTM D 975)
Ibeto et al.,
(2011)
Galadima et
al., (2008)
Specific
gravity
_ 0.88 - 0.95max 0.88 0.84
Kinematic
Viscosity at
40
0
C
mm
2
/ s 5.86 1.9-6.0 1.9-4.1 5.16 -
Flash point
0
C 170 130min 60-80 202
o
C(395.6
o
F
)
-
Cloud point
0
F 57 - -15 to 5 - -
Sulphur
content (by X-
Ray)
% mass 0.025 0.05max 0.05max - -
Distillation
I.B.P
0
C 350 - - - -
10%
0
C 355 - 70max - -
50%
0
C 365 - 125max - -
80%
0
C >400 - 180max - -
E.B.P
0
C _ 360max
Total
recovery
_
97% - - - -
Cetane index _ 49.56 47min 40-55 - -
Ash content % mass 0.016 0.02 - -
Free
glycerine
% mass
0.018 0.02max 0.02 - -
Total
Glycerine
% mass
0.240 0.24max 0.24 - -
Acid value mg
KOH/g
0.210 0.5max - 4.96 0.45
Water by
distillation
% vol Trace 0.05max 0.5max Trace -
Basic water
and Sediment
% vol Trace 0.05max 0.5max Trace 0.02
Table 7. Measured Properties of biodiesel produced
produced was taken at its initial boiling point (IBP), at 10%, 50%, and 80% and at its end
boiling point, the values obtained for each of them were 350
0
C, 355
0
C, 365
0
C and >400
0
C
respectively these values were found to be much higher than the ASTM D 6751 due to the
fact that a vacuum distillation apparatus was used. An acid value of the produced biodiesel
was also measured and the result is presented in Table 7. The acid number correlates to the
fuels long-term stability and corrosiveness, the smaller the acid value, the higher the quality
of the fuel. The acid value of the biodiesel produced was found to be 0.210mgKOH/g, a
Energy Conservation 214
value lower compared to the maximum recommended standard value of 0.5mgKOH/g
(ASTM D 6751) and better than 4.96 and 0.45mgKOH/g reported by Ibeto et al. (2011) and
Galadima et al. (2008) respectively. The Cetane number relates to the readiness of the fuel to
self-ignite when exposed to the high temperatures and pressure in the diesel engine
combustion chamber. The cetane number affects a number of engine performance
parameters such as combustion, stability, drivability, white smoke, noise and emission of
CO. The number is also indicative of the relative fuel stability [55]. The cetane number of the
biodiesel produced was calculated as 49.5, a value above the ASTM acceptable minimum of
47(as expected) which indicates ignition delay and better ignition properties [55].
Also measure and presented in the table of result is the flash point of the produced
biodiesel, which is described as a tendency of a sample of fuel to form a flammable mixture
with air. The flash point of the biodiesel produced was found to be 170
o
C which is greater
than the minimum acceptable value of 130
o
C specified by ASTM D 6751 (Table 7). Cloud
point is a fuel property that is particularly important for the low temperature operability of
diesel fuel. Initially, cooling temperatures cause the formation of solid wax crystal nuclei
that are submicron in scale and invisible to the human eye. The temperature at which crystal
agglomeration is extensive enough to prevent free pouring of fluid is called its pour point
[56]. In this work, the cloud point of the biodiesel was determined as 20
0
F and is in
accordance with the work of Dunn et al., (1996) [57]. These features have implications on the
use of biodiesel in cold weather applications. Free and total glycerin values are indicators of
incomplete esterification reactions and predictors of excessive carbon deposits in the engine
it shows the mono, di and triglycerides molecule in the biodiesel. The total and free glycerin
determined for the biodiesel produced was 0.018wt% and 0.24wt% respectively, both values
were seen to be within the acceptable standard of ASTM D 6751 (Table 7) and also agreed
with finding of Ibeto et al.(2011) except for slight difference in free glycerine which they
obtained 0.02wt%.
The regression model of experimental data with respect to methyl ester conversion can be
determined by least squares method. A statistical analysis was carried out on the
experimental results obtained using analysis of variance (ANOVA). Effects of the four (4)
factors and their interaction effect were estimated. The results of test of statistical
significance in Table 8 shows that the four reaction parameters: molar ratio, temperature,
time and catalyst concentration had different degrees of effects on the ethyl ester yield
percentage with contributions of 11.5022%, 23.2275%, 14.5916% and 2.81534% respectively .
Table 8 shows that temperature had the highest effect of 8.4375 and the highest percentage
contribution on methyl ester yield than other parameters having 23.23% contribution. Molar
ratio showed the least effect of -5.9375 and a %contribution of 14.5916 on methyl ester yield.
Catalyst concentration had an effect of -6.6875 with a percentage contribution of 14.5916%.
The reaction time had an effect of 2.9375 but the least contribution on methyl ester yield
with 2.81534%. It was also observed that the interaction effect between the factors were very
significant. For instance, interactions between two factors such as temperature molar ratio
(A*B) had the highest effect of 6.0625 with the highest percentage contribution (11.9916%)
Production and Characterization of Biofuel from Refined Groundnut Oil 215
Term Effect SumSqr % Contribtion
A-Molar Ratio -5.9375 282.031 11.5022
B-Temperature 8.4375 569.531 23.2275
C-Catalyst Weight -6.6875 357.781 14.5916
D-Reaction Time 2.9375 69.0313 2.81534
AB 6.0625 294.031 11.9916
AC 0.1875 0.28125 0.0114704
AD 4.5625 166.531 6.79174
BC 2.3125 42.7813 1.74477
BD -2.0625 34.0313 1.38792
CD -5.1875 215.281 8.77993
ABC 0.6875 3.78125 0.154213
ABD -5.9375 282.031 11.5022
ACD -0.8125 5.28125 0.215388
BCD 3.3125 87.7813 3.58003
ABCD 1.1875 11.2813 0.460089
Table 8. Effects of reaction parameters on methyl ester yield.
while temperature- reaction time (B*D) had the least effect of -2.0625 with the lowest
percentage contribution of 1.388%. For interactions between three factors for instance,
temperature-catalyst concentration-reaction time (B*C*D) had the highest effect of 3.3125 with
a percentage contribution of 3.58003%, while molar ratio-catalyst concentration-reaction time
(A*C*D) had the lowest effect of -0.8125 with a percentage contribution of 0.2154%. In concise,
the molar ratio and catalyst weight were seen to have negative effect but temperature and
reaction time were seen to have positive effects, while all interactions also had positive effects
with the exception of (B*D), (C*D), (A*B*D) and (A*C*D) which had negative effects. However,
the negativity of interactions is probably due to side reactions such as soaps formation (Vicente
et al., 1998). Table 10 present the variance analysis of the results.
The variance analysis of the results indicates that the Model F-value is 84.69 which implies that
the model is significant as seen on Table6. this table shows the analysis of variance in which
both the main effects(temperature, molar ratio of methanol-to-oil, rection time and catalyst
weight), second order effect (AB, AD, BC, BD, CD), third order effect (ABD, BCD, ABC, ACD)
and the fourth order effect(ABCD) are significant in the regression model but have no
interaction effect. This implies that the values of "Prob > F" less than 0.0500 indicate model
terms are significant. In this case A, B, C, D, AB, AD, BC, BD, CD, ABD, BCD, ABCD are
significant model terms. Values greater than 0.1000 indicate the model terms are not
significant. Stastitical analysis of the results also indicates that S.D. = 1.38; Mean = 89.47; C.V.%
= 1.54; R
2
= 0.9876; R
2
ADJ = 0.9759; R
2
PRED = 0.9502; PRESS = 122.00; Adequate Precision = 28.168.
The "Predicted R-Squared" of 0.9502 is in reasonable agreement with the "Adjusted R-
Squared" of 0.9759. "Adequate Precision" measures the signal to noise ratio. A ratio greater
than 4 is desirable which shows that the ratio obtained 28.168 is adequate.
Energy Conservation 216
The analysis of variance showed that A,B,C,Dwere significant factors. The mathematical
equation models for predicting average methyl ester yield are the final equation in terms of
coded factors (Equation 1) and final equation in terms of actual factors (Equation 2)
Y= 89.47- 2.97A + 4.22B 3.34C + 1.47D + 3.03A * B + 0.094A * C + 2.28A * D + 1.16B * C
-1.03B * D - 2.59C * D + 0.34A * B * C - 2.97A * B * D (1)
- 0.41A * C+ * D 1.66B * C * D + 0.59A * B * C * D
Y= 453 - 95.00000A - 6.25000B - 76.00000C - 4.31111D + 1.62500AB + 34.00000AC
+ 1.21111AD + 1.35000BC + 0.078889BD + 1.06667CD - 0.57500ABC - 0.021111ABD (2)
- 0.60000ACD - 0.023333BCD + 0.010556ABCD.
From Equations 1 and 2, all coefficients in the first and third order term have a minus sign
which indicates that the %methyl ester conversion increases with these factors not
conforming to the experimental result, while coefficients in the second and fourth order
term have plus signs which indicates that the %methyl ester conversion increases with these
factors conforming to the experimental result and also indiccates that there are also
optimums within the experimental condition range.
4. Conclusion
Biodiesel was successfully produced from refined groundnut oil via alkali catalyzed
transesterification using methanol, in the presence of NaOH. The produced biodiesel was
characterized and from the results obtained, the methyl ester produced can be effectively
used in a diesel engine since it meets the requirements of ASTM D 6751. Refined groundnut
oil has also been proved to be a good feedstock for biodiesel as an optimum yield of 99%
was obtained, and the obtained fuel properties such as kinematic viscosity (5.86 mm
2
/s),
flash point (170
o
F), cetane number (49.56), total sulphur content (0.025 wt%), e.t.c. after
detailed characterization of the produced methyl esters of the oil which were within the
standard ascribed by ASTM. Reaction temperature, reaction time, catalyst concentration and
molar ratio of methanol to groundnut oil are the main variables affecting the methyl ester
yield. These variables were optimized using a 2
4
factorial design while the agitation speed
was kept constant at 200rpm and the optimum methyl ester yield (99%) was obtained at
optimum reaction parameters of 40
o
C reaction temperature, 90 minutes reaction time,
0.5wt% catalyst concentration and methanol to oil molar ratio of 6:1.The regression models
by least square method used to predict % methyl ester conversion from groundnut oil
shows that the main effect, first order effect, second order effect, third order and fourth
order effect are significant with no interaction effect, the coefficient of determination R
2
is
0.99. From the analysis of variance, it can be concluded that temperature had the highest
effect and percentage contribution of 8.4375 and 23.2275% respectively to methyl ester yield
from groundnut oil while molar ratio had the lowest effect (-5.9375) and a percentage
contribution of 11.50%. It can also be concluded that from all the interaction effect of the
four (4) reaction variables, A, B, C, D, AB, AD, BC, BD, CD, ABD, BCD, ABCD were
significant model terms. A simple first degree polynomial regression model that can predict
the methyl ester yield from groundnut oil has been developed and represented as:
Production and Characterization of Biofuel from Refined Groundnut Oil 217
Y = = 453 - 95.00000A - 6.25000B - 76.00000C - 4.31111D + 1.62500AB + 34.00000AC
+ 1.21111AD + 1.35000BC + 0.078889BD + 1.06667CD - 0.57500ABC - 0.021111ABD
- 0.60000ACD - 0.023333BCD + 0.010556ABCD.
Based on the results of the various analysis conducted, it can be infered that, groundnut oil
is a good feedstock for methyl ester production especially in Nigeria where it is cheap and
readily available.
Author details
Jimoh A.
, Odigure J.O. and Odili U.C.
Department of Chemical Engineering, School of Engineering and Engineering Technology,
Federal University of Technology, PMB 65 Minna, Niger State, Nigeria
Abdulkareem A.S.
*
Department of Chemical Engineering, School of Engineering and Engineering Technology, Federal
University of Technology, PMB 65 Minna, Niger State, Nigeria
Department of Civil and Chemical Engineering, College of Science, Engineering and Technology,
University of South Africa, Private Bag X6, Florida 1710, Johannesburg, South Africa
Afolabi A.S.
Department of Civil and Chemical Engineering, College of Science, Engineering and Technology,
University of South Africa, Private Bag X6, Florida 1710, Johannesburg. South Africa
Acknowledgment
Step B project, Federal University of Technology, Minna Nigeria is appreciated for their
support. National Research Foundation (NRF), South Africa and Faculty of Science,
Engineering and Technology, University of South Africa are also appreciated for their support.
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Chapter 9
Optimalization of Extraction Conditions for
Increasing Microalgal Lipid Yield by Using
Accelerated Solvent Extraction Method (ASE)
Based on the Orthogonal Array Design
Lin Rulong, Cai Wenxuan, Xing Bingpeng and Ke Xiurong
Additional information is available at the end of the chapter
http://dx.doi.org/10.5772/52475
1. Introduction
Since the fossil fuel crisis broke out in the nineteen seventies with the continual rise in fossil
fuel prices, the mankind has been searching for renewable energy for consumption. For the
past decades, atmospheric pollutions that involve with using fossil fuel have resulted in
many severe problems of environment and human health
[1-16]
. Therefore, exploitation and
utilization of clean and renewable energy have become the strategic consideration for many
countries. Biofuel, as an alternative fuel, is recently attracting increasing attention
[17-20]
.
Microalgae grow in aquatic environments and use light and carbon dioxide to create
biomass and have been recognized as potentially good material sources for biofuel
production. Microalgae possess several aspects of advantages for development of clean
green energy, i.e. they have short growth period and are easy to cultivate and reproduce to
large biomass. Controlled culture conditions of microalgae could trigger high lipid content
of microalgae which could be used for lipid extraction, in turn, by further transesterification
reaction, for preparation and production of biofuel with excellent characteristics. Therefore,
utilization of the microalgal lipid for producing biofuel has promising future
[21-27]
. It should
be noticed that obtaining lipid is a prerequisite for the production of microalgal fuel. More
and more investigations have showed that microalgae are potentially good biomass
materials for development of clean green energy
[28-40]
.
As shown in figure 1, there are six major steps for biofuel preparation and production from
initiating microalgal cultivation to biofuel products. Each of six steps involves with crucial
techniques and methods in order to achieve high production of biofuel. For example, during
Energy Conservation 222
microalgal cultivation, it is very important to screening and selecting fine microalgal strains
with higher oil content for reproduction and amplification of algal cells
[41-45]
. In addition,
investigating on controlled culture conditions that could improve oil accumulation of
microalgal cells is necessary for the increase in biofuel production
[46-51]
. Usually, open ponds
are used in microalgal cultivation with the less expense, simple facilities and operation.
However, its disadvantages are associated with such issues as culture contamination,
difficulties in regulation and control of culture conditions(like temperature and light
control), lower productivity and so on
[52-54]
. Closed system such as photobioreactors(PBRS)
are as well used for microalgal culture. These are highly-automated clear piping systems,
which allow the operator to control nutrients, light, temperature and contamination for high
productivity. But such facilities require expensive investment
[55-59]
. While heterotrophic
culture and amplification of algal cells by using fermentation tanks can obtain highly-
concentrated algal cells for high productivity effects, such facilities are also involved in high
investment cost
[60-61]
. Microalgal harvesting is another crucial technique for entire biofuel
production process. Since microalgal cells are so tiny (only micron order of magnitude in
size) that it is quite difficult for effective microalgal cell harvesting. Taking cost and energy
efficiencies into consideration, a relative simple and feasible method, flocculation of
microalgal cells by changing pH value of culture medium or using certain eco-friendly
chemical and biological flocculants like ferric chloride and chitosan, could be adapted in
harvesting microalgal biomass. During flocculation, the dispersed microalgal cells can
aggregate and form larger conjugates with higher sedimentation rate. Moreover, those
methods allows the cycle reuse of the flocculated medium, thereby contributing to the
economic cultivation and harvest of microalgae
[62-66]
. Harvested microalgal cells can further
be made in form of powers through the process of dehydrating and drying. Optimized
treatment conditions regarding extraction and transesterfication reaction of microalgal oils,
which need to be further developed and explored, as well play an important role in the
effective biofuel target products
[67-70]
.
Due to miniature and hardiness of microalgal cells, it is usually difficult for the extraction of
microalgal lipid component which often requires the operation of special treatment (such as
cell wall breaking, pressurizing and heating etc.) to achieve more complete extraction effect.
Traditionally, there could be several methods used in extraction of microalgal lipid to get
information on lipid content of biological samples, for instance, the Soxhlet extraction
method by using organic solvents for biological sample treatment and sample-heating
treatment with some strong inorganic acids and so on.
[71-74]
.
In spite of simplicity and easiness regarding those methods, obvious disadvantages are
time-consuming for the analysis and operational treatment. Moreover, a considerable
amount of organic solvents or other acid substances, which could involve with human
health problem and the pollution of the environment, are often used in a sample-treating
process. Supercritical CO2 extraction method for extracting biological sample lipid is quite
effective, but it requires expensive equipment to complete sample analysis
[75-76]
..
Optimalization of Extraction Conditions for Increasing Microalgal Lipid Yield by
Using Accelerated Solvent Extraction Method (ASE) Based on the Orthogonal Array Design 223
Figure 1. Schematic diagram of biotechnical process of microalgal biofuel preparation
In order to consume less toxic, less amount of organic solvents and obtain higher algal
lipid yield result, it is crucial to adopt appropriate methods and conditions for lipid
extraction of microalgal materials. Accelerated solvent extraction (ASE) is one of the best
methods for extraction of microalgal lipid with a small amount of organic solvents
needed in extraction treatment. In this investigation, we carried out the experimental
Energy Conservation 224
study on optimalization of extraction conditions for increasing microalgal lipid yield by
using accelerated solvent extraction method based on applying an orthogonal array
design (OAD). Experimental factors including extraction solvent (hexane, chloroform,
petroleum ether, ethanol, acetone), temperature (75-175 C), time (420 min) and
extraction cycle number (15) at five-levels were studied in 25 trials by OAD25 (5
6
) to
reach rapid and high lipid extraction for the marine microalga Nannochloropsis oculata
Droop.
The objectives of this study were:
1) to determine which factors might have more significant effects than the others on the
extraction of microalgal lipid;2) to obtain the optimum level of each tested factor; and 3) to
determine a best combination of the 4 tested factors with 5 factoral levels to be used as
increasing extraction efficiency for microalgal lipid yield.
2. Materials and methods
2.1. Cultivation and treatment of microalgal species for experiment study
The strain of marine microalgaNannochloropsis oculata Droopwas from our laboratory
storage and used for batch culture step by step to sufficient quantity of algal cells. The
microalga was cultivated with general enriched seawater f/2-Si medium designed for
growing coastal marine algae (Guillard and Ryther 1962). The microalga was grown under
regulated and controlled conditions(water temper 25C, light intensity 5000lux, salinity
30,PH 7.8) and harvested during log growth phase. Microalgal cells from collection liquid
were condensed by a centrifugal treatment process and desalinated after two times of
distilled water washing and centrifugal treatment and prepared in form of microalgal
powder by using freeze drying process for extraction of microalgal lipid.
2.2. Chemical reagents and intrument used in the experiment
All chemicals and reagents used in this experimental study were analytical or research
grade without further purification and from Xiamen Luyin Chemical Company.
Intrument accelerated solvent extractor ASE 100 (Dionex) was used for extraction of
microalgal lipid.
2.3. Experimental designation of ASE method for the extraction of microalgal
lipid
Four factors with five levels each were designed for their effects to be investigated on the
extraction of microalgal lipid with orthogonal array design. An orthogonal array table
OAD25 (5
6
) was used for designing ASE experiment of microalgal lipid extraction.
Experimental designation for different factors and levels influencing the extraction of
microalgal lipid was arranged in following table 1.
Optimalization of Extraction Conditions for Increasing Microalgal Lipid Yield by
Using Accelerated Solvent Extraction Method (ASE) Based on the Orthogonal Array Design 225
factor
level
A
extraction solvent
B
extraction tem.
C
extraction time
min
D
extraction cycle
times
1 hexane 75 4 1
2
chloroform 100 8 2
3 petroleum ether 125 12 3
4 ethanol 150 16 4
5 acetone 175 20 5
Table 1. Designation of factors and levels for lipid extraction by ASE method
2.4. Operational method of ASE extraction and instrument analytical conditions
Extraction operation process of microalgal lipid and parameter settings: Appropriate
amount of about 5g (5.120 0.076g) of microalgae powder samples was put into 34ml
extraction pool of the instrument. The extraction pressure value was constant at 1500psi.
Based on combination of different factors and levels of five types of different extraction
solvents (hexane, chloroform, petroleum ether, ethanol, acetone), extraction temperature
range from 75~175 , extraction time range from 4~20 min, extraction cycle number for 1~5
times, corresponding operational treatment of ASE microalgal lipid extraction was adopted
according to 4 factors and 5 levels of orthogonal experiment set(refer to Table2). Other
relevant extraction parameters were constantly set as 60% of flush volume and 90s of purge
time for microalgal lipid extraction. Microalgal lipid extracted was steam-dried by a rotary
evaporator and further dried via N2 gas blowing process and finally dried at 100 for 2
hours. The final microalgal lipid quantity extracted for different ASE operation was
expressed as lipid % based on algal dry weight.
2.5. Conventional Soxhlet extraction method for microalgal lipid
The extraction of microalgal lipid was concurrently conducted by conventional classic
Soxhlet and using same extraction solvents to compare extraction efficiency with ASE
method. Appropriate ammout of microalgal power samples mixed with quartz sand
particles was ground in a mortar and then transferred to extraction cylinder of the extractor.
Solvent extraction included the process with 18 hours of Static extraction and 6 hours of
dynamic extraction to reach a thorough extraction. The final microalgal lipid quantity
extracted was expressed as lipid % based on algal dry weight.
2.6. Calculation of extraction efficiency increase based on ASE and Soxhlet
methods for microalgal lipid
Extraction efficiency increase(EI%) was calculated by formula below:
EI % =100A-S /A
Energy Conservation 226
A and S respectively represent the lipid amount (gram) of microalga extracted by the
methods of ASE and Soxhlet.
2.7. Data analysis and treatment
The arrangement of importance of the four factors to the extraction of microalgal lipid were
evaluated according to the effectiveness of each factor through the calculation of ranges (R
value) (determined from the difference between the maximal and minimal lipid content (%)
within the five levels of each factor), that means, the factor with the most effectiveness (i.e.,
with the largest range of R value) to the extraction of microalgal lipid is considered as the
most important factor, the factor with the lest effectiveness (i.e., with the smallest range of R
value) to the extraction of microalgal lipid is considered as the lest important factor.
Analysis of variance (ANOVA) was conducted to test the significance of the effects of the
four factors on the extraction of microalgal lipid by using statistical software SPSS 15.0. In all
analyses, the level of significance was set at a P-value of 0.05.
3. Results
3.1. The orthogonal experiment result and analysis
The orthogonal experiment result and analysis based on 4 factors and 5 levels was shown in
Table 2 for ASE extraction of microalgal lipid and the associated variance analysis result
shown in Table 3. Variation trend of extraction efficiency of microalgal lipid was shown in
Figure 2 for different extraction operations with various factor level values.
The experimental results indicated that: by using different extraction solvents and various
combinations of different extraction operations, lipid content (% ) had the apparent
difference ( range between 2.98%~21.36%). This suggests that different extraction treatments
on microalgal cells result in the difference in lipid yield of the microalga. Solvents
chloroform, hexane and petroleum ether had normally poor extraction effect on microalgal
cells, and the anhydrous ethanol and acetone were good extraction solvents for microalgal
lipid. Calculation results of range of R value based on table 2 test experiment reflect the size
of the corresponding factor effect. Compared to those factors with smaller R value, the
factors with greater R value are generally significant factors to make remarkable influence
on lipid extraction of microalgal cells since more difference of lipid yield occurs at the
different levels of those factors. Our experimental results showed that, the R values caused
by the extraction solvent, extraction temperature, extraction time and extraction cycles were
respectively 25.91, 38.85, 16.44 and 16.67. Therefore, according to the size of the R values, the
significance of test factors for accelerated solvent extraction (ASE) of microalgal lipid may be
arranged as: extract temperature, extraction solvent, extraction cycle, extraction time.
Variance analysis of the results of accelerated solvent extraction (ASE) processing
experiment data further indicated (Table 3), extraction effect of temperature on the
microalgal lipid was significant (P =0.000515), followed by significant extraction effect of
solvents (P =0.003855).The significant extraction effect of extraction time at significant level
Optimalization of Extraction Conditions for Increasing Microalgal Lipid Yield by
Using Accelerated Solvent Extraction Method (ASE) Based on the Orthogonal Array Design 227
of a =0.05 was also observed (P =0.035094). Comparatively, the effect of extraction cycles on
microalgal lipid was relatively small and it was not significant (P =0.081996) at the
significance level set for a =0.05.
factor
trial no
A
extraction
solvent
B
extraction T
C
extraction time
min
D
cycle
times
lipid (%)
(alga DW)
1 hexane 75 4 1 2.98
2 hexane 100 8 2 5.76
3 hexane 125 12 3 8.52
4 hexane 150 16 4 15.74
5 hexane 175 20 5 16.15
6 chloroform 75 8 3 10.05
7 chloroform 100 12 4 10.21
8 chloroform 125 16 5 13.37
9 chloroform 150 20 1 13.10
10 chloroform 175 4 2 13.92
11 petroleum ether 75 12 5 5.81
12 petroleum ether 100 16 1 5.44
13 petroleum ether 125 20 2 13.32
14 petroleum ether 150 4 3 10.77
15 petroleum ether 175 8 4 13.45
16 ethanol 75 16 2 12.25
17 ethanol 100 20 3 16.09
18 ethanol 125 4 4 14.87
19 ethanol 150 8 5 15.99
20 ethanol 175 12 1 15.86
21 acetone 75 20 4 10.79
22 acetone 100 4 5 10.47
23 acetone 125 8 1 12.74
24 acetone 150 12 2 13.07
25 acetone 175 16 3 21.36
level I 49.15 41.89 53.01 50.12 =302.09
level II 60.65 47.97 58.00 58.33
level III 48.80 62.82 53.47 66.79
level VI 75.06 68.68 68.17 65.06
level V 68.43 80.74 69.45 61.80
Value R 25.91 38.85 16.44 16.67
Table 2. Result and analysis of orthogonal experimentation by ASE method
Energy Conservation 228
source SS df MS F p significance
A. solvent 108.117 4 27.029 9.564 0.003855 ***
B. temperature 197.100 4 49.275 17.435 0.000515 ***
C. time 50.116 4 12.529 4.433 0.035094 **
D. cycle 34.878 4 8.719 3.085 0.081996
error 22.610 8 2.826
sum 412.820 24
SS =Sum of squares; df = degrees of freedom; MS =mean squares
Table 3. Variance analysis of orthogonal experimentation by ASE method
Figure 2. Variation trend of lipid extraction for different factors and levels
Figure 2 also demonstrated the variation trend of extraction effect of microalgal lipid for
different factors and levels of operational conditions based on ASE method. For extraction
solvents, ethanol and acetone had the best extraction effect for microalgal lipid extraction,
followed by hexane and chloroform and solvent petroleum had the poorest extraction effect
for microalgal lipid. The lipid yield raised with an increase in extraction temperature or
extraction time and reached the maximum at a temperature of 175 ,extraction time of
16min and 3 extraction cycles. Therefore for operational simplicity, it was not necessary for
extraction process of microalgal lipid to take more than 16min and 3 extraction cycles.
Taking into consideration the optimal extraction effect for lipid yield of microalgal cells
based on the R values of orthogonal experimental data and the results of variance analysis
of factors and levels, the best operational parameters for ASE method are: using extraction
solvents of ethanol or acetone, extraction temperature of 175 , extraction time of 16min and
3 extraction cycles, which resulted in the highest lipid production. For the health and cost
0
10
20
30
40
50
60
70
80
90
1 2 3 4 5
Factor level
R
a
l
a
t
i
v
e
v
a
l
u
e
f
o
r
l
i
p
i
d
e
x
t
r
a
c
t
i
o
n
e
f
f
i
c
i
e
n
c
y
solvent
temperature
extraction time
extraction cycle
Optimalization of Extraction Conditions for Increasing Microalgal Lipid Yield by
Using Accelerated Solvent Extraction Method (ASE) Based on the Orthogonal Array Design 229
consideration, it is more preferable for using ethanol in lipid extraction operation in due to
its relatively less toxicity and price.
3.2. Validation of optimal ASE extraction conditions and comparison of
extraction effectiveness
Based on the results of orthogonal experiment and data analysis, it was observed that
optimized ASE treatment for the extraction of microalgal lipid was using ethanol or acetone as
solvents with other operational parameters such as 1500psi of extraction pressure, 175 of
extraction temperature, 16 minutes of extraction time and three extraction cycle. To evaluate
the stability and superiority of optimized ASE treatment effect for the extraction of microalgal
lipid, a comparison was made between the optimized ASE treatment and conventional Soxhlet
method for the extraction effectiveness of microalgal lipid. The results were shown in Table 4.
Trial #
ethanolASE acetoneASE
Microalgal
powder (g.dw)
Extracted
lipid(g)
Lipid
%based
on
micro-
algal dw
AI%
Microalgal
powder
(g.dw)
Extracted
lipid(g)
Lipid
%based
on
microalg
al dw
AI%
1 5.0578 0.9805 19.57 44.19 5.0140 0.9810 19.57 39.08
2 5.0637 1.0356 20.45 47.09 5.0616 1.0694 21.13 43.58
3 5.0504 0.9908 19.62 44.85 5.0521 1.0012 19.82 39.85
4 5.0838 0.9779 19.24 43.75 5.2892 1.0763 20.35 41.42
5 5.0735 0.9739 19.20 43.63 5.0856 1.0658 20.96 43.12
6 / / / / 5.0040 1.0687 21.36 44.19
( X )
5.0658 0.9917 19.62 44.70 5.0844 1.0437 20.53 41.87
(SD) 0.0131 0.0253 0.50 1.42 0.1048 0.0414 0.73 2.10
Note: For conventional Soxhlet method, 1.0 gram of microalgal powder was used for lipid extraction using same
extraction solvents. Microalgal yields were respectively 0.1082 gram with calculated lipid % as 10.82% (based on algal
dry weight) for using ethanol extraction and 0.1192 gram with calculated lipid % as 11.92% (based on algal dry weight)
for using acetone extraction.
Table 4. Validation of optimal ASE extraction conditions and comparison of extraction effectiveness
Table four results clearly showed that the fluctuation of lipid extraction yield was very small
and extraction effect was quite stable for optimum processing conditions of accelerated
solvent extraction (ASE) for microalgal lipid extraction. Not only were the extraction process
time and extraction solvent volume considerably saved, but also lipid extraction
effectiveness were greatly improved in ASE method. Compared with conventional Soxhlet
extraction method, ASE method with ethanol as extraction solvent, extraction efficiency
could increase 43.63-47.09% (mean SD 44.70 1.42%). For using acetone as the extraction
solvent extraction efficiency of ASE method could increase 39.08-44.19% (mean SD to 41.87
2.10%). Therefore, adopting the optimum processing conditions of ASE method for
microalgal lipid extraction can reach maximum microalgal lipid yield and its lipid extraction
efficiency is obviously higher than conventional Soxhlet extraction method.
Energy Conservation 230
4. Discussion
The orthogonal array design is a useful experiment methodology,especially for multi-factor
experiment and analysis. It can provide useful and sufficient information for accessing and
evaluating main factors and the optimum combination of factor levels for target parameter
as less experimental trials as possible
[77-80]
. ASE method is approved for use by the U.S. EPA
and CLP Program and a good one for extracts in treating many different samples.
Extractions that normally take hours can be done in minutes using Accelerated Solvent
Extraction (ASE). Compared to techniques like Soxhlet and sonication, ASE generates results
in a fraction of the time. In addition to speed, ASE offers a lower cost per sample than other
techniques by reducing solvent consumption by up to 90%. Relatively less extraction time,
reduction in solvent consumption and wide range of application are the essencial
advantages of ASE method. By using conventional liquid solvents at elevated temperatures
and pressures, ASE increases the efficiency of the extraction process. Increased temperature
accelerates the extraction kinetics, and elevated pressure keeps the solvent below its boiling
point, thus enabling safe and rapid extractions. Although ASE uses the same aqueous and
organic solvents as traditional extraction methods, it uses them more efficiently. ASE can be
used to replace Soxhlet, sonication, wrist shaking, and other extraction techniques typically
used
[81]
.
Because the ASE method requires relatively simple equipment with many aspects of
advantages such as higher degree of automation, good safety, less solvent consumption,
fast-complete extraction and high efficiency , it has been widely applied in analyzing and
testing various types of samples from different sources. For instance, it can be used to detect
the extracts from the water, soil, sediment, minerals, chemical products, biological samples
(vegetables, fruits, meat, fish, plants) and other harmful substances (such as various
pesticides, hydrocarbons, chemicals and the like)
[82-93]
. ASE technology is very important
and helpful for environmental protection and human health. For determination and
evaluation of bio-active components from animals and plants, especially for separation,
extraction and purification of Chinese traditional herb medicines, ASE also played an
important role
[94-97]
. For example, ASE method has been applied for extraction of phenolic
acid compound salvia, volatile oil from Mu Xiang, almond oil from plants, saponin from
Ginseng. Many relevant studies indicate that target product yield and extraction efficiency
are higher by using ASE method than conventional types of extraction techniques
[98-100]
. Our
present study also showed extraction efficiency for microalgal lipid has an increase of 39.08-
47.09% by using ASE method, compared with conventional Soxhlet extraction method. This
suggest that ASE technology has the wide applicability in different fields of sample
extraction.
Due to different features and characteristics with extract of the target products, the
application of ASE method should depend on the actual situations and determine
appropriate parameter settings for extraction processing in order to obtain the practical
optimal extraction results. For example, using methanol as solvent extraction with
Optimalization of Extraction Conditions for Increasing Microalgal Lipid Yield by
Using Accelerated Solvent Extraction Method (ASE) Based on the Orthogonal Array Design 231
extraction parameters set as pressure 1500psi, temperature 140 , time 5 minutes,
extraction cycle number 2, ginseng saponins could reach the maximum extraction amount,
which was 25.88-58.68% of higher than other conventional extraction methods (such as
immersion method, ultrasonic method, homogenization, mechanical vibration method)
[98]
.
Zhang et al (2007) reported the results of extraction of flavonoid compounds in citrus
peels using optimum ASE operational conditions and showed that maximum extraction
rate of target products was obtained with using 80% ethanol as solvent, pressure 10.3Mpa,
temperature 70 , time of 10 minutes, extraction cycle number 1
[99]
. Pang et al (2007) used
uniform experimental design method and reported extraction of almond kernel oil with
the optimum ASE process operations. The results showed that the maximum amount of
oil extraction was obtained by using acetone: hexane (1:3) as solvent, the temperature of
120-140 , time 6-12 minutes, extraction cycle number 1-3
[100]
. Herrero (2005) studied the
extraction of bioactive products for microalga (Spirulina platensis).The optimal ASE
extraction conditions of antioxidant compounds of the microalga were using ethanol as
solvent, temperature 170 , time 3-9 minutes, which resulted in target product extraction
as high as 19.7% (based on algal dry weight) compared to only 2.94-8.22% of antioxidant
compound extraction by using the other three types of solvents (hexane, petroleum ether,
water) in the same extraction conditions
[101]
. This suggests that extraction parameter
setting for target product extraction is crucial for the extraction result of applying ASE
method. In summary, determination of the optimal extraction conditions should depend
on different samples, target products and the experimental designs in application of ASE
method.
Our present study was involved with the extraction of microalgal lipid by using ASE
method. This study clearly showed that an increase of temperature and pressure during
the extraction process could greatly enhance the solvent penetration and diffusion
capacity, thereby result in a rapid extraction of microalgal lipid components. Compared
with the conventional Soxhlet extraction method, ASE method with the optimal
operational conditions could significantly improve the microalgal lipid extraction and
raise 39.08-47.09% of lipid extraction efficiency. For a consideration of security and
practicability, using ethanol or acetone with the lowest toxicity as extraction solvents is
another advantage for sample treatment. Therefore, using ASE method with the
optimization of extraction conditions is suitable for the rapid and efficient extraction of
microalgal lipid.
5. Conclusion
Our findings in the present investigation demonstrated that accelerated solvent extraction
method (ASE) based on the orthogonal array design is an effective approach for the
extraction and determination of lipid content in biological microalgal samples. This study
also demonstrated that the application of multiple-factor and level experimental design
based on Taguchis orthogonal array could determine the optimal extraction operation and
obtain maximal yield for lipid extraction of microalgae.
Energy Conservation 232
Author details
Lin Rulong, Cai Wenxuan, Xing Bingpeng and Ke Xiurong
Key Laboratory of Global Change and Marine-Atmospheric Chemistry,
Third Institute of Oceanography,State Oceanic Administration, Xiamen, China
Acknowledgement
This study was supported by special research project fundings of China National Marine
Public Welfare Industry (grant number200705025 and grant number 200705025).
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