FM DataSheets - Cause and Effect of Fire and Explosions

FM Global
Property Loss Prevention Data Sheets
7-0
April 2013
Page 1 of 22
CAUSES AND EFFECTS OF FIRES AND EXPLOSIONS
Table of Contents
Page
1.0 SCOPE ................................................................................................................................................... 3
1.1 Changes ............................................................................................................................................ 3
2.0 GENERAL ............................................................................................................................................... 3
3.0 BASIC DEFINITIONS AND PRINCIPLESFIRE ................................................................................. 3
3.1 Combustion ...................................................................................................................................... 3
3.2 Ignition Temperature ........................................................................................................................ 3
4.0 IGNITION SOURCES ............................................................................................................................. 3
4.1 Electrical .......................................................................................................................................... 4
4.2 Static Electricity ............................................................................................................................... 4
4.3 Hot SurfacesNonelectrical ........................................................................................................... 5
4.4 Sparks and Open FlamesHot Work ............................................................................................. 5
4.5 Smoking ........................................................................................................................................... 5
4.6 lncendiarism ..................................................................................................................................... 6
4.7 Spontaneous Ignition ....................................................................................................................... 6
5.0 INDICATORS OF SLOW OR FASTBURNING FIRES ..................................................................... 12
6.0 EFFECTS OF FIRE ON STEEL ........................................................................................................... 13
6.1 Thermal Expansion ........................................................................................................................ 13
6.2 Loss of Strength ............................................................................................................................ 13
6.3 Thermal Conductivity ..................................................................................................................... 13
6.4 Evaluating Structural Damage ....................................................................................................... 13
7.0 EFFECTS OF FIRE ON CONCRETE AND MASONRY ...................................................................... 13
8.0 EFFECTS OF FIRE ON WOOD ........................................................................................................... 14
9.0 EFFECTS OF FIRE ON SPRINKLER SYSTEM .................................................................................. 14
10.0 BASIC DEFINITIONS AND PRINCIPLESEXPLOSIONS .............................................................. 15
10.1 Explosion ..................................................................................................................................... 15
10.2 Physical Explosion ....................................................................................................................... 15
10.3 Chemical Explosion ..................................................................................................................... 16
10.4 Thermal Explosion ....................................................................................................................... 16
10.5 BLEVE ......................................................................................................................................... 16
10.6 Deflagration ................................................................................................................................. 16
10.7 Detonation ................................................................................................................................... 16
10.8 The Mechanism of Explosion ...................................................................................................... 16
10.9 The Buildup Period ...................................................................................................................... 16
10.10 The Triggering Agent ................................................................................................................. 17
10.11 Explosion Prevention ................................................................................................................. 17
11.0 EFFECTS OF EXPLOSIONS ............................................................................................................. 17
11.1 Detonations .................................................................................................................................. 17
11.1.1 Energetic Materials ............................................................................................................. 17
11.1.2 Blast Waves and Overpressures ......................................................................................... 18
11.1.3 Craters ................................................................................................................................. 18
11.2 Deflagrations ................................................................................................................................ 19
11.3 Vapor Cloud Explosions (VCE) ..................................................................................................... 19
11.4 Vessel Ruptures and BLEVES .................................................................................................... 19
11.4.1 Pressure Vessel Rupture Failure Pressure ......................................................................... 20
2006-2013 Factory Mutual Insurance Company. All rights reserved. No part of this document may be reproduced,
stored in a retrieval system, or transmitted, in whole or in part, in any form or by any means, electronic, mechanical,
photocopying, recording, or otherwise, without written permission of Factory Mutual Insurance Company.
7-0
Causes and Effects of Fires and Explosions
Page 2
FM Global Property Loss Prevention Data Sheets
11.4.2 Pressure Vessel Rupture Energy Release .......................................................................... 20

11.4.3 Loss Examples .................................................................................................................... 20
12.0 REFERENCES ..................................................................................................................................... 20
12.1 FM Global ...................................................................................................................................... 20
12.2 Others ............................................................................................................................................ 20
APPENDIX A GLOSSARY OF TERMS ....................................................................................................... 21
APPENDIX B DOCUMENT REVISION HISTORY ....................................................................................... 22
List of Figures
Fig. 1. Examples of pressure & impulse profiles from deflagration (left) and detonation ........................... 15
Fig. 2. Damage after the explosion. ............................................................................................................ 21
List of Tables
Table
Table
Table
Table
1. Color of Smoke Produced by Burning Combustibles ....................................................................... 6

2. Materials Subject to Spontaneous Heating1 .................................................................................... 7
3a. Scaled Ground Distance at Overpressures (English) ................................................................... 18
3b. Scaled Ground Distance at Overpressures (Metric) ..................................................................... 18
2006-2013 Factory Mutual Insurance Company. All rights reserved.

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Page 3
1.0 SCOPE
This data sheet is designed to provide information useful to those evaluating fires and explosions. It does
not include recommended safeguards.
Refer to Data Sheet 7-42, Guidelines For Evaluating the Effects of Vapor Cloud Explosions Using a Flame
Acceleration Model, for specific details on outdoor vapor cloud explosions and methods to evaluate the blast
effects on property.
1.1 Changes
April 2013. Minor editorial changes and additional guidance for using TNT equivalence methods for estimating
the effects of explosions (overpressure) involving energetic materials.
2.0 GENERAL
With fire, two factors are of major importance. These are the cause or ignition source and the development
of the fire. Determination should be made as to how fire could start and how it could develop, spread, be
controlled, and extinguished.
In an explosion, events prior to explosion are important. An explosion is a rapid transformation of potential
physical or chemical energy into mechanical energy. It is important to determine how the potential energy can
be accumulated or prepared for sudden transformation and how this transformation can be triggered. The
effects of an explosion may be explored to evaluate its magnitude.
3.0 BASIC DEFINITIONS AND PRINCIPLESFIRE
3.1 Combustion
Combustion is an exothermic chemical reaction usually involving oxidation of a fuel by atmospheric oxygen.
Glowing combustion involves direct oxidation of a solid or liquid fuel, such as charcoal or magnesium.
Flaming combustion involves a gas phase or volatile matter driven off by heat.
3.2 Ignition Temperature
Ignition temperature is the minimum temperature to which a substance must be heated to initiate selfsustained combustion in whatever atmosphere is present. To start the chemical reaction between fuel
molecules and oxygen molecules, sufficient energy must be imparted into the mix. If the fuel is a solid or liquid,
some of it usually is turned into a gas (unless the oxidizer is also a solid or liquid) so that there is intimate
mixing of molecules. The ignition temperature can vary, depending on the fuel or oxygen concentration, the
rate of air flow, rate of heating, the size and shape of the solid or space involved, the temperature of the
ignition source, and possible catalytic or inhibiting effect of other materials present.
For less volatile solids, such as wood, or paper, the ignition temperature is greatly dependent on the time
necessary to volatilize the fuel to form an ignitable mix at the surface. Artificial heating can also initiate
self-heating, which may bring the fuel up to its ignition temperature. The normally accepted minimum
self-ignition temperature of wood, paper, cotton, wool, and combustible fiberboards is 400 to 500F (200
to 260C). Ignition can occur at lower temperatures if the material is contaminated with oils or if charcoal is
formed followed by ensuing self-heating.
4.0 IGNITION SOURCES
An ignition source is normally energy in the form of heat which brings fuel up to its ignition temperature.
Since fires are unusual in most occupancies, an ignition source usually involves some unusual circumstance
not otherwise present. Ignition sources are classified based on the origin of the heat involved.
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4.1 Electrical
Electrical energy produces heat when electric current flows through a conductor or jumps an air gap. The
heat produced is proportional to the resistance and to the square of the current. Excessive heat, sufficient to
start a fire, can be generated by: (1) a high current, (2) a high resistance, or (3) impaired cooling or removal
of normal heat.
1. High current can be the result of:
a. Short circuits caused by breakdowns in insulation or accident. Continuous overload causing a short
before the fire will exhibit beads of metal and fusing of the copper wire conductors. There will also be
decomposition and carbonization of insulation on both sides where the short occurred. Shorts caused
during the heat of the fire may show beading. However, decomposition and carbonization of insulation
will be found only on the side exposed to the fire.
b. Single phasing in three-phase motors. (See Data Sheet 5-18, Protection of Electrical Equipment.)
c. Loss of field in synchronous motors. (See Data Sheet 5-13, Synchronous Motors.)
d. Lightning. (See Data Sheet 5-11, Lightning Surge Protection.)
2. High resistance can be the result of loose or oxidized electrical connections.
3. Impaired cooling can be the result of:
a. Failure of fans in transformers or enclosed equipment.
b. Plugging of air passageways.
c. Coatings on bare wires, bus bars, lighting fixtures, and heating elements.
d. Dropping of oil or other coolant levels away from heating elements.
e. Combustibles too close to light bulbs or heating elements.
When electric current jumps an air gap, the resistance is so high that even a small current produces significant
energy. In the case of static sparks, minute currents can ignite flammable vapors or gases. Strong currents
arcing across air gaps can melt metal, which in turn can start fires.
If electric motors are found in the area of origin, check the interior of the motor windings to see if the fire
was deep seated; the wire coating at the interior would probably not burn away unless the wiring was heated
electrically.
In any electrical appliance having a thermal control, sticking or fusing of the contact points would signify
overheating of the device.
4.2 Static Electricity
Fires and explosions are often attributed to static electricity after other possible causes have been eliminated.
If a fire or explosion is caused by static electricity, it is important to understand and explain the specific
mechanism so that repetition can be prevented.
For static electricity to be a source of ignition, four conditions must be fulfilled:
1. There must be an effective means of static generation.
2. There must be a means of accumulating the charges and maintaining a suitable electrical potential
difference.
3. There must be a spark discharge of adequate energy.
4. The spark must occur in an ignitable mixture.
Static is normally generated by movement of dissimilar substances involving the making and breaking of
contact of surfaces. A poor conductor of electricity must be involved. Examples are a rapidly moving rubber
belt; paper or cloth unwinding or passing over rollers; nonconducting fluids flowing through pipes or being
agitated in tanks; or the movement of dust or stock, as in grain handling.

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A free charge on an ungrounded conductive body is mobile, and the entire charge can be drawn off by a
single spark. On the other hand, the charge on a nonconductive body is relatively immobile so that a spark
from its surface can release the charge from only a limited area and will usually not involve enough energy
to produce ignition. Thus, nonconductors, the bodies most directly involved in charge generation, are usually
not directly involved in the sparks which initiate fires and explosions.
For example, if a person walks across a fur rug, static electricity will be generated by the nonconductor, the
rug, and accumulated in the body of the person, a nongrounded conductor. When the person touches a
grounded object, a spark will jump at that point.
A static spark is a relatively weak ignition source. The most common ignitable mixture is a mixture of a
flammable vapor or gas with air. A liquid involved normally must be above its flash point. Combustible dust
mixtures may possibly be ignited by static electricity, but it requires a very high energy spark. Static sparks
do not normally have sufficient energy to ignite dusts.
4.3 Hot SurfacesNonelectrical
Combustible or flammable material may be ignited by contact with or by radiant heat from surfaces heated
by means other than electrical energy. These hot surfaces are most often produced by: (1) friction, (2)
heating equipment, and (3) molten substances.
1. Friction can be caused by improperly lubricated bearings, broken or misaligned machine parts, choking
or jamming of materials, and poor adjustment of conveyors or machine drives. Frictional heating may cause
noncombustible parts to become hot and ignite nearby combustibles. A typical example is a hot paper
machine bearing igniting oil or paper lint. In some instances, the combustible material may be heated directly,
as with a rubber conveyor belt slipping on a pulley.
Friction, as a fire cause, will be indicated if the point of damage to the motor belts is worse where it passes
over pulleys. In fires from outside sources, belts are damaged most between pulleys.
2. Heating equipment located too close to combustible construction or storage can result in ignition. The
top or bottom of a furnace or heater, a hot flue or duct, or an exposed steam pipe may ignite combustibles
in contact with the heated surface or where nearby clearances, insulation, or air circulation is adequate.
The ordinary ignition temperature of wood is 400 to 500F (200 to 260C), but when wood is exposed to
prolonged heat, it undergoes a chemical change and becomes pyrophoric carbon with an ignition temperature
as low as 300F (150C). Heat will greatly reduce the time required for ignition. For instance, long leaf pine
will ignite when subjected to: 356F (180C) for 14.3 minutes; 392F (200C) for 11.8 minutes; 437F (225C)
for 8.7 minutes; 482F (250C) for 6.0 minutes; 572F (300C) for 2.3 minutes; 662F (350C) for 1.4 minutes;
and 752F (400C) for 0.5 minutes.
3. Molten substances, such as metal or glass escaping from a furnace or container, can ignite any
combustible material in the vicinity.
4.4 Sparks and Open FlamesHot Work
Open flames may be fixed or portable. Fixed open flames, such as in ovens, furnaces, water heaters, and
boilers, may ignite moving combustibles, such as flammable vapors or gases. Portable flames, such as
portable burners or welding torches, can ignite combustible material any place in a building. Hot sparks or
molten globules from cutting or welding or from mechanical grinding operations are common ignition sources.
Metal introduced into textile or grain processing machinery can generate hot sparks that can ignite lint, dust,
or other easily ignitable material.
4.5 Smoking
Smoking is a leading cause of fires. This conclusion is often determined by a process of elimination. Direct
evidence is seldom found which proves that a cigarette, cigar, or match was specifically the ignition source.
Studies have been made of the mechanisms by which cigars and cigarettes start fires. Temperatures in a
glowing cigarette range from 550 to 1400F (290 to 760C). Test conclusions were:
1. Cigars and cigarettes start fires in solid fuels (except explosives, matches, and other highly flammable
chemicals) by first initiating glowing combustion. Therefore, in order to be ignitable by a cigarette, a solid must
be capable of supporting flameless combustion. Such materials are virtually all of cellulosic origin and include
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paper, fabric, textile fibers, and dry vegetation. Materials which melt when heated, such as rubber, plastic,
and most synthetic fibers, cannot sustain glowing combustion, possibly because the heat applied is absorbed
as heat of fusion during the melting stage.
2. Conditions favoring ignition include a good supply of finely divided, fairly compact fuel and a good air
supply or draft to promote flaming combustion.
3. Flammable vapors and gases are surprisingly difficult to ignite with a cigar or cigarette, but not impossible.
Cigarettes are an unreliable source of ignition, but their widespread use and careless handling make them
significant as a fire cause. Of course, flames from matches or lighters are much stronger and more reliable
ignition sources.
4.6 lncendiarism
An incendiary fire is often characterized by a conscious attempt to insure that the fire is severe. Ignitable
liquids or trailer devices are often used to help spread the fire. Strong ignition sources are used, usually
with a timing mechanism such as a candle or clock. More than one fire is often started at once. Fire protection
systems may be shut off. In accidental fires, chance plays an important part. In intentional fires, chance is
minimized.
Witnesses to the fire in its early stages can often give helpful information concerning the material initially
involved in the fire. If incendiarism is suspected, the type of smoke or flame initially observed is often of
interest.
Color of smoke is often the first clue to the combustibles involved in the fire (Table 1).
Table 1. Color of Smoke Produced by Burning Combustibles
Combustible
Hay/Vegetable compounds
Cooking oils
Phosphorus
Nitrocellulose
Sulfur
Sulfuric, nitric, or hydrochloric acid
Gunpowder
Chlorine gas
Petroleum products
Wood
Most plastics
Paper
Cloth
Color of Smoke
White
Brown
White
Yellow-Brownish-Yellow
Greenish-Yellow
Black
Gray-Brown
Black
Gray-Brown
Gray-Brown
The absence of flames or comparatively small flames indicate a lack of air. More flames than smoke indicate
well-ventilated burning of dry substances. Erratic flames indicate the presence of gases, while sparks in large
quantities indicate that powdery substances are burning.
A trailer (a line of paper rags or ignitable liquid designed to cause a fire to spread) often leaves residue, or
a fire spreads in ways other than its usual upward direction.
4.7 Spontaneous Ignition
Spontaneous heating can occur in many types of materials including solids (wood chips, coal, foam rubber,
rags, fiberboard, and metal powders) and liquids (animal and vegetable oils). Materials that spontaneously
heat will increase in temperature without taking heat from the surrounding environment. Heat generations is
generally due to one or a combination of the following exothermic reactions (reactions that liberate heat):
oxidation (chemical combination of a material with oxygen), decomposition (material breaks down into its
elements), polymerization (combination of low molecular weight molecules into a single high molecular weight
compound), or biological action (bacterial caused decomposition). These reactions often occur normally (at
a slow rate) without heat build-up. An increase in material temperature occurs when heat loss to the
surroundings is reduced. The conditions that will affect spontaneous heating include: the geometry of the

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material, the available surface area and insulation from the surrounding environment. Various arrangements
of the above reactions and other conditions will permit spontaneous heating to occur and lead to the ignition
of the material producing either flaming or smoldering combustion.
In agricultural crops, bacteria can promote oxidation and heat generation. This can be promoted by a high
moisture content. The bacteria tends to die at temperatures above 160 to 175F (71 to 80C); heating
beyond that point is normally due to oxidation accompanied by chemical decomposition.
The following materials are most subject to spontaneous heating:
1. Animal and Vegetable Oils. These oils contain unsaturated bonds, having greater tendency for oxidation
at lower temperatures. The greatest danger occurs if they impregnate rags or other absorbent, insulating
organic materials.
2. Agricultural and Animal Products. These may contain animal or vegetable oils, or may be subject to bacterial
oxidation. If heated, or if already charred, the oxidation tendency is increased.
3. Wood Chips. See Data Sheet 8-27, Storage of Wood Chips and Data Sheet 7-10, Wood Processing and
Woodworking Facilities.
4. Coal and Charcoal. See Data Sheet 8-10, Coal and Charcoal Storage.
5. Fiber Products. These products are most hazardous when heated and stored before cooling, or when
impregnated or contaminated with animal or vegetable oils.
6. Paint and Paint Scrapings. The most hazardous are paints which are not fully dry and contain linseed
oil or drying agents. High gloss paint designed to dry at room temperature contains drying agents. These
oxidizing catalysts strongly promote spontaneous heating when arranged so that heat cannot readily dissipate
as in stored scrapings. See Data Sheet 7-27, Spray Application of Ignitable and Combustible Materials.
Table 2, Materials Subject to Spontaneous Heating, lists additional materials that should be evaluated.
Table 2. Materials Subject to Spontaneous Heating1
(Originally prepared by the NFPA Committee on Spontaneous Heating and Ignition which has been discontinued. Omission
of any material does not necessarily indicate that it is not subject to spontaneous heating.)
Name
Alfalfa Meal
Burlap Bags Used
Tendency to
Spontaneous
Heating
High
Usual Shipping
Container or
Precautions Against
Storage Method
Spontaneous Heating
Bags, bulk
Avoid moisture extremes.
Tight cars for
transportation are
essential
Possible
Bales
Castor Oil
Very slight
Metal Barrels,
Metal Cans in
Wooden boxes
Charcoal
High
Bulk, Bags
Moderate
Bulk
Coal, Bituminous
Keep cool and dry.
Avoid contact of leakage

from containers with rags,
cotton, or other fibrous
combustible materials.
Keep dry. Supply
ventilation.
Store in small piles. Avoid

high temperatures.
Remarks
Many fires attributed to
spontaneous heating probably
caused by sparks, burning
embers, or particles of hot metal
picked up by the meal during
processing. Test fires caused in
this manner have smoldered for
72 hours before becoming
noticeable.
Tendency to heat dependent on
previous use of bags. If oily
would be dangerous.
Possible heating of saturated
fabrics in badly ventilated piles.
Hardwood charcoal must be

carefully prepared and aged.
Avoid wetting and subsequent
drying.
Tendency to heat depends upon
origin and nature of coals. High
volatile coals are particularly
liable to heat.
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Name
Cocoa Bean Shell
Tankage
Coconut Oil
Tendency to
Spontaneous
Heating
Moderate
Usual Shipping
Container or
Precautions Against
Storage Method
Spontaneous Heating
Burlap Bags, Extreme caution must be
Bulk
observed to maintain safe
moisture limits.
Very slight
Drums, Cans,
Glass
Cod Liver Oil
High
Drums, Cans,
Glass
Colors in Oil
High
Drums, Cans,
Glass
Slight High
Bulk Burlap
Bags, Paper
Bags, Bulk
Moderate
Barrels, Tank
Cars
Low Moderate
Bags, Bulk
Barrels, Tank
Cars
Distillers Dried
Grains with oil
content (Brewers
grains)
(Ditto) No oil
content
Moderate
Bulk
Moderate
Bulk
Feeds, various
Moderate
Bulk, Bags
Fertilizers Organic,
inorganic,
combination of both
matter
(Ditto)Mixed,
Synthetic
containing nitrates
and organic
Moderate
Bulk, Bags
Avoid extremely low or

high moisture content.
Moderate
Bulk, Bags
Avoid free acid in

preparation.
Fish meal
High
Bags, Bulk
Fish Oil
High
Fish Scrap
High
Copra Corn-Meal
Feeds
Corn Oil
Cottonseed
Cottonseed Oil

cotton or other fibrous
Keep cool and dry.
Materials should be
processed carefully to
maintain safe moisture
content and to cure before
storage.
Keep Cool and Dry. Avoid
contact of leakage from
containers with rags,
Maintain moisture 7
percent to 10 percent.
Cool below 100F (38C)
before storage.
Maintain moisture 7
percent to 10 percent.
Cool below 100 F (38C)
before storage.
Avoid extremely low or
high moisture content.
Keep moisture 6 percent

to 12 percent. Avoid
exposure to heat.
Barrels, Drums, Avoid contact of leakage
Tank Cars
Bulk, Bags
Avoid moisture extremes.
Remarks
This material is very
hygroscopic and is liable to
heating if moisture content is
excessive. Precaution should be
observed to maintain dry
storage, etc.
Only dangerous if fabrics, etc.,
are impregnated.
Impregnated organic materials

are extremely dangerous.
May be very dangerous if

fabrics, etc., are impregnated.
Heating possible if wet and hot.

Usually contains an appreciable
quantity of oil which has rather
severe tendency to heat.
Dangerous heating of meals,

etc., unlikely unless stored in
large piles while hot.
Heating possible if piled wet
and hot. May cause heating of
saturated material in badly
ventilated piles.
Very dangerous if moisture
content is 5 percent or lower.
Very dangerous if moisture

content is 5 percent or lower.
Ground feeds must be carefully

processed. Avoid loading or
storing unless cooled.
Organic fertilizers containing
nitrates must be carefully
prepared to avoid combinations
that might initiate heating.
Insure ventilation in curing
process by small piles or
artificial drafts. If stored or
loaded in bags, provide
ventilation space between bags.
Dangerous if over dried or
packaged over 100F (38C).
Impregnated porous or fibrous
materials are extremely
dangerous. Tendency of various
fish oils to heat varies with
origin.
Scrap loaded or stored before
cooling is extremely liable to
heat.

Name
Foam Rubber in
Consumer Products
Tendency to
Spontaneous
Heating
Moderate
Usual Shipping
Container or
Precautions Against
Storage Method
Spontaneous Heating
Bulk, Bags
Where possible remove
foam rubber pads, etc.
from garments to be dried
in dryers or over heaters.
If garments containing
foam rubber parts have
been artificially dried, they
should be thoroughly
cooled before being piled,
bundled, or put away.
Keep heating pads, hair
dryers, other heat sources
from contact with foam
rubber pillows, etc.
Bulk, Bags
Avoid moisture extremes
Grain (various
kinds)
Hay
Very slight
Moderate
Bulk, Bales
Keep dry and cool
Hides
Very slight
Bales
Keep dry and cool.
Iron Pyrites
Moderate
Bulk
Istle
Very slight
Bulk, Bales
Avoid large piles. Keep

dry and cool.
Keep cool and dry.
Jute
Very slight
Bulk
Lamp Black
Very slight
Lanolin
Negligible
Lard Oil
Slight
Lime, unslaked
(Calcium Oxide,
Pebble Lime,
Quicklime)
Linseed
Linseed Oil
Manure
Menhaden Oil
Metal Powders*
Moderate
Wooden Cases Keep cool and dry.
Glass, Cans,
Metal Drums,
Barrels

Wooden Barrels Avoid contact of leakage
Paper Bags,
Keep dry. Avoid hot
Wooden
loading.
Barrels, Bulk
Very slight
Bulk
High
Tank, Cars,
Drums, Cans,
Glass
Moderate
Bulk
Moderate to
high
Moderate
Keep cool and dry.
Keep cool and dry.

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Remarks
Foam rubber may continue to
heat spontaneously after being
subjected to forced drying as in
home or commercial dryers, and
after contact with heating pads
and other heat sources. Natural
drying does not cause
spontaneous heating.
Ground grains may heat if wet

and warm.
Wet or improperly cured hay is
almost certain to heat in hot
weather. Baled hay seldom
heats dangerously.
Bacteria in untreated hides may
initiate heating.
Moisture accelerates oxidation
of finely divided pyrites.
Heating possible in wet
materials. Unlikely under
ordinary conditions. Partially
burned or charred fiber is
dangerous.
Avoid storing or loading in hot
wet piles. Partially burned or
charred material is dangerous.
Fires most likely to result from
sparks or included embers, etc.,
rather than spontaneous
heating.
Heating possible on
contaminated fibrous matter.
Dangerous on fibrous
combustible substances.
Wetted lime may heat

sufficiently to ignite wood
containers, etc.
Tendency to heat dependent on
moisture and oil content.
Rags or fabrics impregnated
with this oil are extremely
dangerous. Avoid piles, etc.
Store in closed containers,
preferably metal.
Avoid storing or loading
uncooled manures.
Avoid extremes of low or

high moisture contents.
Ventilate the piles.
Barrels, Drums, Avoid contact of leakage
Dangerous on fibrous product.
Tank Cars
Drums, etc.
Keep in closed containers. Moisture accelerates oxidation
of most metal powders.
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Name
Metal Turnings*
Mineral Wool
Mustard Oil, Black
Oiled Clothing
Usual Shipping
Tendency to
Container or
Precautions Against
Spontaneous
Storage Method
Spontaneous Heating
Heating
Practically none
Bulk
Not likely to heat
spontaneously.
None
Pasteboard
Noncombustible. If loaded
Boxes, Paper hot may ignite containers
and other combustible
Bags
surroundings.
Low
Barrels
with rags, cotton or other
fibrous combustible
materials.
High
Fiber Boxes
Dry thoroughly before
packaging.
Oiled Fabrics
High
Oiled Rags
High
Oiled Silk
High
Oleic Acid
Very slight
Oleo Oil
Very slight
Olive Oil
Moderate to
Low
Paint containing
drying oil
Moderate
Paint Scrapings
Moderate
Palm Oil
Low
Peanut Oil
Low
Peanuts, Red
Skin
High
Peanuts, shelled
Very slight or
Negligible
Perilla Oil
Moderate to
High
Remarks
Avoid exposure to sparks.
This material is mentioned in
this table only because of
general impression that it heats
spontaneously.
Avoid contamination of fibrous
Dangerous if we material is
stored in piles without
ventilation.
Rolls
Keep ventilated. Dry
Improperly dried fabrics
thoroughly before packing. extremely dangerous. Tight rolls
are comparatively safe.
Bales
Avoid storing in bulk in
Dangerous if we with drying oil.
open.
Fiber Boxes,
Supply sufficient
Improperly dried material is
Rolls
ventilation.
dangerous in form of piece
goods. Rolls relatively safe.
Glass Bottles, Avoid contact of leakage
Impregnated fibrous materials
Wooden Barrels from containers with rags, may heat unless ventilated.
May heat on impregnated
from containers with rags, fibrous combustible matter.
Tank Cars,
Drums, Cans, from containers with rags, may heat unless ventilated.
Tendency varies with origin of
Glass
oil.
Fabrics, rags, etc. impregnated
Drums, Cans, Avoid contact of leakage
Glass
from containers with rags, with paints that contain drying
oils and driers are extremely
dangerous. Store in closed
containers, preferably metal.
Barrels, Drums Avoid large unventilated
Tendency to heat depends on
state of dryness of the
piles.
scrapings.
form containers with rags, may heat unless ventilated.
oil.
combustible materials
Wooden
form containers with rags, may heat unless ventilated.
Barrels, Tin
Cans
oil.
Paper Bags,
Avoid badly ventilate
This is the part of peanut
Cans, Fiber
storage.
between outer shell and peanut
Board Boxes
itself. Provide well ventilated
Burlap Bags
storage.
Paper Bags,
Keep cool and dry.
Avoid contamination of rags,
Cans, Fiber
etc., with oil.
Board Boxes,
Burlap Bags
Tin Cans,
Barrels
from containers with rags, may heat unless ventilated.
oil.

Name
Pine Oil
Tendency to
Spontaneous
Heating
Moderate
Powdered Eggs
Very slight
Powdered Milk
Very slight
Rags
Variable
Usual Shipping
Container or
Precautions Against
Storage Method
Spontaneous Heating
Glass, Drums Avoid contact of leakage
Wooden Barrels Avoid conditions that
promote bacterial growth.
Inhibit against decay.
Keep cool.
Avoid conditions that
Wooden and
promote bacterial growth.
Fiber Boxes,
Inhibit against decay.
Metal Cans
Keep cool.
Bales
Avoid contamination with
drying oils. Avoid charring.
Keep cool and dry.
Glass Bottles, Avoid contact of leakage
Wooden Barrels from containers with rags,
Rolls, Bales,
Avoid over-drying the
Crates
material. Supply
ventilation.
Red Oil
Moderate
Roofing Felts and

Papers
Moderate
Sawdust
Possible
Bulk
Scrap Film (Nitrate)
Very slight
Drums and
Lined Boxes
Scrap Leather
Very slight
Bales, Bulk
Scrap Rubber or
Buffings
Moderate
Bulk, Drums
Sisal
Very slight
Bulk, Bales
Soybean Oil
Moderate
Tin Cans,
Barrels, Tank
Cars
Sperm Oil -See

Whale Oil
Tankage
Variable
Bulk
Tung Nut Meals
High
Paper Bags,
Bulk
Moderate
Tin Cans,
Barrels, Tank
Cars
Turpentine
Low
Tin, Glass,
Barrels
Varnished Fabrics
High
Boxes
Tung Oil
Avoid contact with drying

oils. Avoid hot, humid
storage.
Film must be properly
stabilized against
decomposition.
7-0
Page 11
Remarks
may heat unless ventilated.
oil.
Possible heating of decaying
powder in storage.
Possible heating by decay or

fermentation.
Tendency depends on previous

use of rags. Partially burned or
charred rags are dangerous.
Impregnated porous or fibrous
materials are extremely
dangerous. Tendency varies
with origin of oil.
Felts, etc., should have
controlled moisture content.
Packaging or rolling uncooled
felts is dangerous.
Partially burned or charred
sawdust may be dangerous.
Nitrocellulose film ignites at low

temperature. External ignition
more likely than spontaneous
heating. Avoid exposure to
sparks, etc.
Avoid contamination with
Oil-treated leather scraps may
drying oils.
heat.
Buffings of high rubber
Sheets; slabs, etc. are
content should be shipped comparatively safe unless
and stored in tight
loaded or stored before cooling
containers.
thoroughly.
Keep cool and dry.
Partially burned or charred
material is particularly liable to
ignite spontaneously.
Avoid contact with rags,
may heat unless well ventilated.
cotton, or fibrous
materials.
Avoid extremes of
moisture contents. Avoid
loading or storing while
hot.
Material must be very
carefully processed and
cooled thoroughly before
storage.
Process carefully. Keep
cool and ventilated.
Very dry or moist tankages

often heat. Tendency more
pronounced if loaded or stored
before cooling.
These meals contain residual oil
which has high tendency to
heat. Material also susceptible
to heating if over-dried.
oil.
Has some tendency to heat but
less so than the drying oils.
Chemically active with chlorine
compounds and may cause fire.
Thoroughly dried varnished
fabrics are comparatively safe.
7-0
Page 12
Usual Shipping
Container or
Storage Method
Wrapped
Bundles,
Pasteboard
Boxes
Bales
Name
Wallboard
Tendency to
Spontaneous
Heating
Slight
Waste Paper
Moderate
Whale Oil
Moderate
Barrels and
Tank Cars
Wool Wastes
Moderate
Bulk, Bales,
Etc.
Precautions Against
Spontaneous Heating
Maintain safe moisture
content. Cool thoroughly
before storage.
Keep dry and ventilated.
Keep cool and ventilated
or store in closed
containers. Avoid high
moisture.
Remarks
This material is entirely safe
from spontaneous heating if
properly processed.
Wet paper occasionally heats in
storage in warm locations.
oil.
Most wool wastes contain oil,
etc. from the weaving and
spinning and are liable to heat
in storage. Wet wool wastes are
very liable to spontaneous
heating and possible ignition.
* Refers to iron, steel, brass, aluminum, and other common metals, for information on magnesium, sodium, zirconium, etc.
1
Reprinted with permission from Fire Protection Handbook, 18th edition, Copyright 1997, National Fire protection Association, Quincy,
MA 02269.
The ignition source for a recent large loss was directly attributed to the spontaneous ignition of used rags.
The plant had recently switched from a chlorofluorocarbon (CFC) based solvent to a terpene based solvent.
The terpene solvent resolved several environmental concerns, however, it also introduced a combustible
liquid into a process that previously had none. Used clean-up rags containing terpene solvent were discarded
into open top plastic trash barrels where the fire started.
Sources of terpenes are turpentine and other basic oils. Terpene solvents are used as a CFC solvent
replacement because they are considered environmentally safe (used for circuit board cleaning). The material
safety data sheet for the solvent involved indicated the liquid could polymerize. Chemically, terpenes can
have unsaturated bonds which would suggest spontaneous heating tendencies (confirmed by the example
loss). Proper disposal (normally closed metal containers) and prompt removal (empty drums at end of shift)
of the terpene soaked rags would have eliminated the ignition source and prevented this loss.
The potential for spontaneous heating needs to be considered as a possible ignition source in many
occupancies. Recognition of a material that may spontaneously heat, allows the initiation of preventative
measures designed to eliminate or control the potential ignition source. Changes in manufacturing materials
to comply with new codes and laws must be fully reviewed to assure a clear understanding of any new
hazards that are introduced by the changes.
Spontaneous ignition can also take place by other exothermic chemical action, sometimes sudden and violent
if highly reactive materials are mixed. Examples are water and sodium, strong oxidizing materials, and
organic matter. NFPA 491M, Manual of Hazardous Chemical Reactions, gives many specific examples.
5.0 INDICATORS OF SLOW OR FASTBURNING FIRES
Uniform overhead damage usually indicates a slow and smoldering fire, whereas extensive damage in one
place on the ceiling indicates an intense, rapid buildup beginning below this spot. A wide angle V pattern
indicates a slow-burning fire. A narrow angle V indicates a fast-burning fire.
In glass, large cracks and a heavy smoke film generally indicate slow burning, while irregularly shaped cracks
and slight smoke film generally indicate rapid burning. A fast, intense fire will cause heavy alligatoring and
shiny, smooth blisters on exposed wood surfaces, while a long, low heat source will produce flat alligatoring.
In a cross-section of a piece of wood found near the point of origin, a distinct line between charred and
uncharred portions of the wood indicates a fast, intense fire. A gradation in charring and an overall baked
appearance usually indicate a long, slow fire.

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6.0 EFFECTS OF FIRE ON STEEL

Steel has three characteristics that are of concern under fire conditions:
1. Steel expands substantially when heated.
2. Steel loses strength substantially when heated to temperatures in excess of 900 to 1000F (480 to
540C).
3. Steel transmits heat readily.
6.1 Thermal Expansion
If the ends of a steel member are free to move, the increase in length is approximately 0.065 percent for
each 100F rise in temperature (0.125 percent for each 100C rise in temperature). For example, a 100 ft
(30 m) long steel beam heated uniformly to 1000F (556C) above ambient will increase in length by almost
8 in. (200 mm). If the ends are fixed, the applied stress will change by about 19,000 psi for each 100F
temperature change (240 MPa [2400 bars] for each 100C). Uniform heating of long horizontal beams can
push over masonry walls or cause shear failure in connections for structural steel members.
Analysis of fire-induced stresses in horizontal cylindrical tanks containing liquefied gas indicates that failure
of such tanks under fire conditions is not due to overpressurization nor to weakening of the unwetted shell,
but to stresses produced by the axial expansion of the unwetted portion of the shell. As the unwetted portion
is heated, it tends to expand, while the immediately adjacent wetted portion of the shell remains cool and
restrains the expanding portion. As a result, tensile stress in excess of the ultimate strength of the metal is
produced just below the liquid level. The metal starts to rip circumferentially at that point. The tank separates
into (usually two) sections which rocket parallel to the axis of the tank.
6.2 Loss of Strength
The strength of mild steel actually increases up to about 600F (315C). Beyond that temperature, a decrease
in strength occurs until about 1100F (600C) when the strength of steel is reduced to a point where it is
not sufficient to carry the dead load, and the steel member fails.
Loss of strength is often the result of localized heating due to shielding or obstruction of the water spray
from a few sprinklers or due to missing sprinklers. Bar joists and steel trusses are particularly subject to failure
due to rapid overheating of thin steel members. The consequences in the case of bar joists may not be
serious because large supporting beams that are protected can maintain the overall structural integrity of
the building. However, localized overheating of a small section of a large steel truss system can cause major
building collapse.
6.3 Thermal Conductivity
Heat can be transmitted through steel to combustible material that is otherwise unexposed to fire, such as
steel deck roof insulation and contents of tanks and bins.
6.4 Evaluating Structural Damage
Mild structural steel building members often show no change in physical properties as a result of fire exposure.
Many instances have been reported where straightening of distorted structural steel members has been both
feasible and economical. Connections between members should be checked for cracks around holes.
Steel which has been exposed to temperatures of 1600F (870C) or higher may have a roughened
appearance due to excessive scaling and grain coarsening. The steel will usually have a dark gray color,
although other colors may be present. Steel so modified is commonly called burnt steel. Its suitability for
further use is a matter for careful evaluation and judgment.
Steel with a higher carbon content than mild structural steel often has special characteristics determined
by heat treating. Fire exposure may significantly change its physical properties and affect its suitability for
continued use.
7.0 EFFECTS OF FIRE ON CONCRETE AND MASONRY
Fire alone seldom causes failure of concrete or masonry structural components. Failure is more often due
to loss of support or stresses indirectly resulting from the fire. For example:
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Masonry walls can be pushed over by expanding concrete or steel members, toppling or expanding storage,
or explosion pressures.
Exposed steel-supporting trusses, beams, or columns can fail if not protected by water spray or insulation.
Floors can be overloaded by water-soaked storage.
Spalling can occur due either to expansion of moisture or to thermal expansion of the outer surface in concrete
under compression as in columns, walls, or prestressed structural members.
Damage to concrete is usually superficial in fires with automatic sprinkler protection or in fires lasting less
than two hours without sprinklers. If exposure is more severe, a careful study of structural damage is needed.
A waiting period of several weeks will allow damage to concrete to be more discernible from cracking,
layering, calcination, or discoloration. The natural gray color changes to pink or brown indicating exposure
to temperatures in excess of 450F (232C). Unsound concrete will be more or less soft and friable when
chipped with a pick or hammer. Core samples of concrete and samples of reinforcing steel for load tests
give more accurate quantitative measurements of structural strength. Such tests and examination should be
performed under the supervision of a registered structural engineer.
Loss of tension in prestressed concrete-reinforcing tendons should be investigated where these members
have been heated above 300F (150C). Ordinary reinforcing steel should be restored to its depth of cover
where spalling has occurred to preserve its protection against future fire exposure and corrosion.
8.0 EFFECTS OF FIRE ON WOOD
Although wood is combustible, it has some positive properties from a fire exposure standpoint. For example,
it does not expand significantly when heated, it does not lose strength except as it is burned away, and it
is much less conductive than steel or concrete.
Thin members, such as boards and joists, burn through or lose strength much more rapidly than planks or
plain or laminated timbers. The average rate of penetration of char when flame is impinged upon a wood
member is about 112 in. (40 mm) per hour. This is often useful in tracing the origin of a fire in an area of
wood construction or occupancy.
Fire tends to sweep upward until its progress in this direction is blocked by some obstacle. If no holes, cracks,
or outlets are present, the flames mushroom out horizontally until they bend around the obstruction and
continue upward. Fire does not spread nearly so rapidly in a horizontal direction unless there are favorable
ventilation conditions or some fast-burning material present. Fire should not spread downward significantly
except in the case of falling, burning material. This also may be useful in tracing the origin of a fire.
Charring of the top surface of a wood floor is usually not evident because flames tend to rise away from
the surface, and water from fire fighting readily protects the surface. However, localized charring is often
evident. This can indicate the presence of either a combustible surface just above the floor such as a skid
radiating heat downward or a thin ignitable liquid layer burning on the floor with some soaking-in to increase
the volatility of the wood. It can also indicate a fire near the floor where water cannot penetrate to the floor
because of shielding above or absorption by material above such as tissue or plastic foam.
Except for the volume of wood lost to charring, the strength of a wood structural member is affected very
little by fire exposure. After the charred volume has been deducted, the remaining strength can be determined
through structural analysis. However, metal-connecting members such as bolts and screws may lose strength
or lose their connecting ability due to the burning away of wood.
9.0 EFFECTS OF FIRE ON SPRINKLER SYSTEM
The effect of the fire on the automatic sprinkler system can furnish useful information. This involves two
factors: the number of sprinklers that operate, and the damage done to the sprinkler system by the fire.
The operation of an unusually high number of sprinklers can be due to a variety of causes:
1. A water supply too weak for the hazard.

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Page 15
2. The water supply to the sprinklers shut off, either at the start of the fire or during the fire. This may be
due to:
a. a closed valve,
b. broken pipe,
c. obstructed pipe,
d. a dry pipe or deluge valve that failed to open or which was delayed,
e. impairment of a water supply.
3. Shielded sprinklers
4. Fire that spread ahead of the sprinkler operation due to:
a. dust, oil, or lint deposits, usually near the ceiling;
b. fast-burning construction such as plastic foam, usually at the ceiling;
c. an explosion or puff of vapor or dust;
d. sprinklers located too far below the ceiling.
Damage to sprinklers, piping, or valves indicates that the equipment damaged did not receive water at some
time during the fire. The extent of the damage should correspond to the extent of the impairment. A few
damaged sprinklers may mean a plugged branch line. A damaged dry-pipe valve may mean an entire system
was shut off and drained.
10.0 BASIC DEFINITIONS AND PRINCIPLESEXPLOSIONS
10.1 Explosion
An explosion is a rapid transformation of potential physical or chemical energy into mechanical energy and
involves the violent expansion of gases. This gas expansion creates a blast wave, with an overpressure
and duration depending on the type of explosion. The two parameters of the blast wave that are important
for evaluation of its damage potential are the maximum overpressure (Pmax) and the impulse (I) of the positive
phase of the pressure-time curve. Figure 1 illustrates the different pressure time profiles of deflagration and
detonation waves.
Pmax
Pmax
Fig. 1. Examples of pressure & impulse profiles from deflagration (left) and detonation
10.2 Physical Explosion

A physical explosion originates from purely physical phenomena, such as rupture of a boiler or pressurized
container, or from interaction between water and molten metal or black liquor smelt.
Flash vaporization, the rapid vaporization of a superheated liquid when the pressure has been suddenly
released, is an example of a physical explosion. This phenomenon often occurs when water is trapped under
hot oil.
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10.3 Chemical Explosion

A chemical explosion originates from a chemical reaction such as a flammable vapor air explosion, a dust
explosion, or detonation of an explosive or blasting agent.
10.4 Thermal Explosion
A thermal explosion is the result of an exothermic reaction occurring under conditions of confinement with
inadequate cooling. As the temperature rises, the reaction rate and heat generation accelerate until the
container falls due to overpressure. See Data Sheet 7-49, Emergency Venting of Vessels.
10.5 BLEVE
A BLEVE (boiling liquid expanding vapor explosion) results from the rupture of a vessel containing a liquid
substantially above its atmospheric boiling point. It may be a physical explosion or a thermal explosion. Energy
is produced by the expanding vapor and boiling liquid. If the vapor is flammable and is ignited, a fireball
ensues. Since the vapor is not premixed with air, if ignition is immediate, the main effect of the combustion
is fire and radiant heat rather than explosive force (overpressure effects). A BLEVE can occur with a
nonflammable liquid as with a rupturing hot water heater.
10.6 Deflagration
A deflagration is an exothermic reaction that propagates from the burning gases to the unreacted material
by conduction, convection, and radiation. The combustion zone progresses at a rate that is less than the
velocity of sound in the unreacted material. The unreacted material may be compressed by the force exerted
by the deflagration, and the reaction rate may increase as a result. If this continues for a sustained time, as
in a pipeline, the reaction rate may increase to sonic velocity, and a detonation may result.
10.7 Detonation
A detonation is an exothermic reaction propagating at greater than sonic velocity in the unreacted material.
A shock wave is established and maintains the reaction. Detonations usually take place in solid or liquid
materials such as explosives or blasting agents, and on rare occasions, explosions in gases can reach
detonation velocity if confined for considerable distances as in pipelines.
10.8 The Mechanism of Explosion
Since an explosion is the rapid transformation of potential physical or chemical energy into mechanical energy,
a common sequence of events takes place in all explosion processes.
1. Preceding the explosion, there is a buildup period during which the potential physical or chemical energy
accumulates in a manner in which it may be suddenly transformed.
2. At the instant of the explosion, a triggering agent is introduced into the system which initiates the energy
transformation.
3. During the buildup period, the triggering agent must be absent.
10.9 The Buildup Period
The buildup period may be anything from a fraction of a second to hours or days. During this time, the stage
is being set for the explosion. Examples are:
1. A cloud of flammable gas or vapor mixes with air, leading to a gas or vapor/air explosion.
2. A cloud of dust mixes with air, leading to a dust explosion.
3. Pressure builds up in a tank, leading to a vessel rupture.
4. Molten metal or black liquor smelt accumulates, leading to a molten substance/water explosion.
5. A charge of explosive material is placed, leading to a blasting explosion.
6. A chemical reaction in a vessel runs away, leading to a thermal explosion.

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10.10 The Triggering Agent

The triggering agent may be introduced into the system, or the buildup period may spread or travel to
encompass the triggering agent.
1. An ignition source, such as a spark or flame, may be introduced into an enclosure after a cloud of
flammable vapor or gas is mixed with air, or the vapor/air cloud expands or moves to encompass the ignition
source.
2. A dust/air cloud contacts a spark or flame sufficient for ignition.
3. The walls of a vessel rupture, transforming the potential physical energy into the expanding mechanical
energy of the gas.
4. Water contacts a hot molten material converting the heat energy into expanding vapor.
5. A detonator or other shock-producing device detonates an explosive material.
6. Failure of a vessel wall converts the thermal chemical energy into a BLEVE or vessel-rupture explosion.
The thermal explosion process itself may have been initiated by sudden mixing of two chemicals.
10.11 Explosion Prevention
The explosion may be prevented or transformed into a controlled release of energy by preventing the buildup
period or the triggering agent, or by insuring that the triggering agent is present during the buildup period:
1. A vapor/air explosion can be prevented by excluding the flammable vapor from the system, by keeping air
out of the system, by preventing any chance of ignition, or by insuring that an ignition source is present when
air and fuel are first introduced, as at the burner of a furnace.
2. A dust explosion can be averted by preventing the formation of dust/air clouds, by keeping ignition sources
away from dust/air clouds, or by (in the case of a pulverized fuel burner) insuring that an ignition source is
present when pulverized fuel is dispersed.
3. A vessel rupture explosion can be averted by preventing a pressure buildup beyond safe limits, by insuring
that the vessel walls do not fail below the maximum allowable pressure, and by releasing the energy by
opening the vessel (through a relief valve or rupture disk) before excessive pressure buildup takes place.
4. A water/molten material explosion can be prevented by excluding molten material, by keeping water from
contacting molten material, or by introducing the molten material in very small quantities to absorb the energy
gradually, as in the dissolving tank of a black liquor boiler.
5. A blasting explosion may be prevented by keeping explosives out of the area, or by keeping detonating
agents away from the explosives.
6. A thermal explosion can be prevented by controlling the exothermic reaction, by adequate cooling or other
reaction suppression devices and by the gradual release of energy by venting devices.
11.0 EFFECTS OF EXPLOSIONS
Explosion effects are from the sudden release of mechanical energy in the form of pressure as a blast wave.
Buildings can be destroyed or damaged by the pressure as well as the duration of the pressure.
11.1 Detonations
Detonations release a very large amount of energy within a relatively small volume. Extremely high pressures
are produced in the immediate vicinity of the detonating material and the explosion occurs too quickly for
venting to have any effect. As a result, there is usually shattering or pulverizing of steel or concrete, and a
crater may be formed. Detonations can occur in some explosives, highly reactive gases (e.g., hydrogen) or
even less-reactive gas-air mixtures in piping systems.
11.1.1 Energetic Materials
Energetic materials, such as TNT, dynamite, rocket propellants, and ammonium nitrate, etc., can accidentally
explode during manufacture or storage causing widespread damage. TNT equivalence is an appropriate
way to evaluate the effects of energetic material explosions and is discussed in Data Sheet 7-28, Energetic
Materials.
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11.1.2 Blast Waves and Overpressures

Blast waves are a major consequence of all explosions and move outward in a spherical shape like the ripple
of a stone dropped in a pool of water. The amplitude (overpressure) and duration are related to the amount
of energy released and how quickly it is released. The blast wave energy (overpressure and duration) decays
at a rate proportional to the cube root of the distance from the explosion (Hopkinson-Cranz Scaling Law).
The common practice in predicting effects of explosion has been to translate the energy released into TNT
equivalent. Most common explosives have TNT equivalents. Other references are available for estimating
the TNT equivalence of other phenomena (Lees, Stephens).
Using the scaling law (Equation 1) it is then possible to predict blast effects in terms of overpressure.
Rg = Zg (We)1/3
(Eq. 1)
Where:
Rg = Radial distance from energy release epicenter (expressed in feet or meters), at some overpressure
Zg = Scaled ground distance (ft/lb1/3 [m/kg1/3]) from Table 3a or 3b for a defined overpressure
We =TNT equivalent mass, expressed in pound or kilograms
Table 3a. Scaled Ground Distance at Overpressures (English)
Overpressure, P
(psig)
15
10
6
5
3
2
1
Scaled Ground Distance, Z

ft/lbs 1/3
8
9.8
13
14.5
19.5
26
45
Table 3b. Scaled Ground Distance at Overpressures (Metric)

Overpressure, P (barg)
1.03
0.69
0.41
0.34
0.21
0.14
0.07
Scaled Ground Distance, Z

m/kg 1/3
3.2
3.89
5.2
5.75
7.7
10.0
17.9
After calculating the distance to the selected overpressure the overpressure rings can be plotted on a plan
view of the site centered on the explosion.
Damage tables based on overpressure are available from a number of sources (Lees, Stephens). There
are also effects related to the duration (impulse), but for most property loss evaluations this was generally
not considered. More recently, evaluations have been done considering both overpressure and impulse.
11.1.3 Craters
If a detonation takes place near the surface of the ground, a crater may be produced. The size of the crater
can vary widely, but an approximation can be made for dry soil by using the formula D = 1.5 W1/3 where
D is the crater diameter in feet, and W is the charge weight in pounds of TNT. In metric units, D = 0.6 W1/3
where D is the crater diameter in meters, and W is the charge weight in kilograms of TNT. The depth of the
crater is normally about one-quarter of the diameter.

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11.2 Deflagrations
Deflagrations release energy more slowly and the combustion occupies a larger volume. The overpressures
developed are less than those from a detonation, and venting of the building or vessel can often reduce
the damage effects to an acceptable level. Damage is more likely to involve tearing of materials into relatively
large pieces. Craters are usually not produced.
11.3 Vapor Cloud Explosions (VCE)
In most deflagrations, the overpressures produced in the explosion are confined to process equipment or a
building. In some cases, such as at petrochemical plants or refineries, a large cloud of flammable vapor can
be released outdoors into a partially confined and/or congested open process structure. The resulting VCE
can produce severe damage over a wide area, sometimes even beyond the plant boundaries. Refer to Data
Sheet 7-42, Guidelines for Evaluating the Effects of Vapor Cloud Explosions using a Flame Acceleration
Model, for details on vapor cloud explosions.
TNT equivalence methods have been used in the past to predict blast effects of vapor cloud explosions but
are no longer widely used for hazard evaluations. Energy release effects from explosives, blast wave and
impulse, are different from that caused by flammable vapor clouds and pressure vessel ruptures, and using
TNT equivalents can overestimate near field effects and underestimate the far field effects.
Flame acceleration models (FAM) for prediction of outdoor gas clouds are more accurate and have been
implemented by FM Global for property loss evaluation. Details are covered in Data Sheet 7-42.
11.4 Vessel Ruptures and BLEVES
When a vessel containing a gas under pressure ruptures, the mechanical energy released is proportional
to the volume of gas times the pressure, assuming that is the only energy available. If the vessel comes apart
completely so that all the energy is released at once, a shock wave may be produced. However, if the
pressure buildup is relieved, for example by a manhole cover coming off, the vessel may remain largely intact
and the energy is released over a longer period. Damage may be limited to that done by the flying cover
or rocketing tank.
If the material in a vessel is noncombustible, the effects of the overpressure will be a blast wave proportional
to the mechanical energy released plus fragments from the vessel. If the material in the vessel is corrosive,
in addition to blast and fragment effects, widespread damage to process areas from later corrosion might
occur. If the material is an ignitable liquid or flammable gas, a number of add on events could occur, such
as a fire ball with radiant heat effects and subsequent fires.
If the vessel contains liquid well above its atmospheric boiling point, a portion of the liquid instantly vaporizes
when the pressure is released. The unvaporized liquid is carried with the expanding vapors and the event
is often called a BLEVE (boiling liquid expanding vapor explosion). The liquid doesnt have to be flammable
to be considered a BLEVE.
Historically, a number of scenarios have resulted in pressure vessel ruptures in process equipment and mobile
storage vessels, including the following:
Process vessels operating in corrosive conditions
Process vessels with potential for internal hidden corrosion such as lined, clad, or overlaid construction
Process vessels with external hidden corrosion, such as under exterior insulation
Vessels with known metallurgical defects
Chemical reactors running exothermic reactions with incorrectly sized, plugged, or impaired pressure relief
devices
Vessels with the potential to be connected to high-pressure services (e.g., air, steam, or process lines)
where the pressure is significantly greater than the ultimate failure pressure of the vessel (MAWP plus
design safety factors)
Process vessels weakened by exposure to an uncontrolled fire
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11.4.1 Pressure Vessel Rupture Failure Pressure

The pressure at which a vessel fails can vary depending on operating conditions, defects, and overpressure
scenarios. Pressure vessels typically have an ultimate failure pressure with a safety margin above the design
maximum allowable working pressure (MAWP). For ASME code vessels this margin can be 3.5 to 4 times
the MAWP, depending on the version or section of the code that applies. European design codes typically have
smaller safety margins, such as 2.4 times MAWP for carbon steel without corrosion or fabrication allowances.
Determine the pressure at vessel failure based on one of the criteria below:
A. Use the highest normal operating pressure of a vessel
in corrosive service or environment.
with known metallurgical defects.
B. Use the ultimate failure pressure (MAWP plus design safety factors) of a vessel
containing highly reactive systems (exothermic reactors).
that can be accidentally exposed to pressure exceeding the ultimate failure pressure.
11.4.2 Pressure Vessel Rupture Energy Release
If energy contained in a pressurized vessel is released by sudden failure of the shell, the effects can be
estimated using pressure-volume (bursting pressure vessel) calculation models. There are a number of
models to estimate the energy release from a bursting pressure vessel. An isothermal expansion model was
previously suggested to tie in with the TNT equivalent method. FM Global has developed proprietary
software, BlastCalc, which will be used by FM Global engineers for pressure vessel rupture evaluations. The
energy release is based on Brodes constant volume energy addition approach tied in with pressure wave
parameters from bursting vessels.
Chapter 7 of the CCPS Guideline book on vapor cloud explosions (see 12.2) provides some guidance on
calculation methods as well as worked examples for evaluating blast effects produced by these events.
11.4.3 Loss Examples
11.4.3.1 Kaiser Aluminum and Chemical Corporation, Gramercy, Louisiana, USA
On July 5, 1999 an explosion occurred at an alumina refinery. The incident occurred in a high-pressure
alumina ore processing system that had been weakened by corrosion and reportedly had impaired pressure
relief systems. The accident caused the rupture of all five digesters in the process. Four of the five digesters
had volumes of 68,000 gal (260 m3), and one had a capacity of 180,000 gal (690 m3). The design
temperature was 600F (315C) and the MAWP was 600 psig (41 barg). Records show the failure pressure
of the vessels was between 600 and 633 psig (41 and 44 barg).The ruptures essentially destroyed the
processing plant. There were no ensuing fires. The gross loss estimate was over US$500 million. This incident
was investigated by the US Mine Safety and Health Administration (MSHA) and a report was issued.
12.0 REFERENCES
12.1 FM Global
Data Sheet 7-12, Mining and Ore Processing Facilities
Data Sheet 7-28, Energetic Materials
Data Sheet 7-42, Guidelines for Evaluating the Effects of Vapor Cloud Explosions using a Flame Acceleration
Model
Data Sheet 7-55, Liquefied Petroleum Gas
Data Sheet 7-64, Aluminum Industry
Data Sheet 7-89, Ammonium Nitrate and Mixed Fertilizers containing Ammonium Nitrate
12.2 Others
Brode, H.L. Blast Wave from a Spherical Charge. Physics of Fluids 2(2): 217-219.
Center for Chemical Process Safety (CCPS). Guidelines for Vapor Cloud Explosion, Pressure Vessel Burst,
BLEVE and Flash Fire Hazards. Second Edition. 2010.

7-0
Page 21
Fig. 2. Damage after the explosion.
Lees, F.P. Loss Prevention in the Process Industries. 2nd Edition. Elsevier, 1996.
Stephens, M.M. Minimizing Damage to Refineries from Nuclear Attack, Natural, and Other Disasters. US
Dept. of the Interior, Office of Oil and Gas, Prepared for the Department of the Army, Series Report No.
AD-773-048. February 1970.
US Department of Labor, Mine Safety and Health Administration (MSHA). Nonfatal Exploding Vessels
Accident, Gramercy Works, Kaiser Aluminum and Chemical Corporation. ID No. 16-00352. July 5, 1999.
APPENDIX A GLOSSARY OF TERMS
Ignitable Liquid: Any liquid or liquid mixture that is capable of fueling a fire, including flammable liquids,
combustible liquids, inflammable liquids, or any other reference to a liquid that will burn. An ignitable liquid
must have a fire point.
Ultimate failure pressure: Internal pressure at which a vessel will fail catastrophically. For ASME code vessels
this pressure can be 3.5 to 4 times the MAWP, depending on the version or section of the code that applies.
European design codes typically have smaller safety margins, such as 2.4 times MAWP for carbon steel
without corrosion or fabrication allowances.
MAWP: maximum allowable working pressure is the maximum pressure to which a vessel may be subjected
during operation. It is code limited and determined by either the manufacturer or by analysis. The value is
usually stamped on the vessel nameplate.
7-0
Page 22
APPENDIX B DOCUMENT REVISION HISTORY

April 2013. Minor editorial changes and additional guidance for using TNT equivalence methods for estimating
the effects of explosions (overpressure) involving energetic materials.
October 2012. References to the use of TNT equivalence to evaluate the effects of vapor cloud explosions
were replaced with the use of flame acceleration modeling and pressure-impulse effects. Additional guidance
was provided for estimating the effects of pressure vessel rupture using pressure-impulse methods to evaluate
the explosion effects.
January 2012. Terminology related to ignitable liquids has been revised to provide increased clarity and
consistency with regard to FM Globals loss prevention recommendations for ignitable liquid hazards.
April 1994. Revised to remove guidance on vapor cloud explosions to new 7-0S.
July 1981. First publication.

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FM Global

Property Loss Prevention Data Sheets

CAUSES AND EFFECTS OF FIRES AND EXPLOSIONS

Causes and Effects of Fires and Explosions

FM Global Property Loss Prevention Data Sheets

11.4.2 Pressure Vessel Rupture Energy Release .......................................................................... 20

1. Color of Smoke Produced by Burning Combustibles ....................................................................... 6

2006-2013 Factory Mutual Insurance Company. All rights reserved.

Causes and Effects of Fires and Explosions

2006-2013 Factory Mutual Insurance Company. All rights reserved.

Causes and Effects of Fires and Explosions

FM Global Property Loss Prevention Data Sheets

2006-2013 Factory Mutual Insurance Company. All rights reserved.

Causes and Effects of Fires and Explosions

2006-2013 Factory Mutual Insurance Company. All rights reserved.

Causes and Effects of Fires and Explosions

FM Global Property Loss Prevention Data Sheets

2006-2013 Factory Mutual Insurance Company. All rights reserved.

Causes and Effects of Fires and Explosions

Burlap Bags Used

Keep cool and dry.

Avoid contact of leakage

Store in small piles. Avoid

Hardwood charcoal must be

2006-2013 Factory Mutual Insurance Company. All rights reserved.

Causes and Effects of Fires and Explosions

FM Global Property Loss Prevention Data Sheets

Cod Liver Oil

Avoid extremely low or

Avoid free acid in

Avoid contact of leakage

Keep moisture 6 percent

Avoid moisture extremes.

Impregnated organic materials

May be very dangerous if

Heating possible if wet and hot.

Dangerous heating of meals,

Very dangerous if moisture

Ground feeds must be carefully

2006-2013 Factory Mutual Insurance Company. All rights reserved.

Causes and Effects of Fires and Explosions

Keep dry and cool

Keep dry and cool.

Avoid large piles. Keep

Wooden Cases Keep cool and dry.

Avoid contact of leakage

Keep cool and dry.

Keep cool and dry.

Ground grains may heat if wet

Wetted lime may heat

Avoid extremes of low or

2006-2013 Factory Mutual Insurance Company. All rights reserved.

Causes and Effects of Fires and Explosions

Mustard Oil, Black

FM Global Property Loss Prevention Data Sheets

2006-2013 Factory Mutual Insurance Company. All rights reserved.

Causes and Effects of Fires and Explosions

Roofing Felts and

Scrap Film (Nitrate)

Sperm Oil -See

Tung Nut Meals

Avoid contact with drying

Possible heating by decay or