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6-Supercritical Fluid Chromatography SFC
6-Supercritical Fluid Chromatography SFC
Chromatography
Aurelia Leyva and Trang Duong
Chem 230
11/30/2010
1
Chapter 33
Supercritical-Fluid
Chromatography
Supercritical-fluid chromatography (SFC), in
which the mobile phase is a supercritical
fluid, is a hybrid of gas and liquid
chromatography that combines some of the
best features of each. For certain
applications, it appears to be clearly
superior to both gas-liquid and highperformance liquid chromatography.
Supercritical Fluid
Substance at a T
and P above critical
point
Effuse through
solids like a gas and
dissolve materials
like a liquid
Close to critical
point, small
changes in T or P
results in large
changes in density
www.che.tohoku.ac.jp
SCF Extractions
The main advantages of using
supercritical fluids for extractions is that
they are inexpensive, contaminant free,
and less costly to dispose of safely than
organic solvents.
Supercritical fluid CO2 is used to extract
caffeine from coffee.
Flavours for brewing are extracted from
hops using SCF extraction.
SFC Instrumentation
Solvent delivery system
Injector
Column/Column Oven
Restrictor
Detector
Data System
SFC Apparatus
http://www.cee.vt.edu/ewr/environmental/teach/smprimer/sfc/sfc.html
1
3
14
Restrictor
Back pressure regulator is very important
or gas P will drop in column
May let SFC convert to gas before
detector
SCF Chromatography
High pressures are used so that the SCF is
much more dense (102-103 x) than a gas
Thus it has better solvating properties
but still not as dense as a liquid
For chromatography we want:
low viscosity coefficient (gas)
Low diffusion coefficient (liquid)
The values of these for SCFs are intermediate
High MW compounds that cant be separated by
GC can be analyzed by SFC.
Compound Tc C
31.3 72.9
CO2
C2H4
9.9
Pc atm
0.96
50.5
N2O
36.5
72.5
NH3
132.5 112.5
--0.94
0.40
n-C5
196.6 33.3
0.51
n-C4
152.0 37.5
0.50
CCl2F2
CHF3
111.8
25.9
d*
40.7
46.9
1.12
----
Supercritical Fluid
Chromatography (SFC)
Property
Density (g/cm 3 )
Diffusion coefficient
(cm 2 /s)
Viscosity (G Cm -1 s -1 )
Gas (STP)
(0.6-2) x 10 -3
(1-4) x 10 -1
SCF
0.2-0.5
10 -3 x 10 - 4
Liquid
0.6-2
(0.2-2) x 10 -5
(1-4) x 10 - 4
(1-3) x 10 - 4
(0.2-3) x 10 -2
2
4
Types of Injectors
a. Loop injection
-Low pressure feed pump needed to fill
the loop
-Mostly for preliminary tests of column
performance and elution parameters
b. In-line injection
-Flexibility for changing injected volume
-High-pressure pump required to inject
feed solution
-Injected stream dissolved in eluent flow
c. In-column injection
-Permits injection of the feed solution
directly onto the column
-No dilutions required
Journal of Liquid Chromatography & Related Technologies, 28: 12331252, 2005
2
5
25
Injectors
Typical HPLC design injectors for
packed columns.
Split/Splitless valve injector (0.01 to
0.05 L injections) for open tubular
columns.
Timed - split injector (0.01 to 0.05 L
injections) for open tubular columns.
Injector Volumes
Open tubular columns
Injection volumes >96nL
Greater volume affects resolution
Packed columns
Injection volumes >1uL
2
7
Column
Open Tubular
- Smaller column diameter more efficient
- Efficiency decreases at high density (decrease u)
* Decrease column diameter
* Increase T (increase diffusion, solubility, volatility)
- Minimal pressure drop effect
2
8
28
Column
Packed
- Packing reduces permeability and creates flow resistance, L <25cm
- Efficiency increases with increasing density (Dm decreases)
- Smaller particle size = smaller H, but increase pressure drop, and decrease
permeability
- Large P drop effect (density decreases, solubility decreases along column length)
2
9
Column
Retention Time
Packed capillary
- Lower volumetric flow rate = more compatible with mass flow
detector, greater sensitivity in conc. detector, easier sample
transfer in multi-D system, higher permeability-longer column
J.W. King, H.H. Hill, and M.L. Lee. 1993
3
0
Stationary Phase
Same as those for GC and LC, with some modification.
Silica/Alumina
Useful for non-polar compounds
Lead to irreversible adsorption of some polar solutes
Bonded to provide less adsorptive packing material
Octyl, octadecyl, cyanoalkyl, aminoalkyl, diolakyl
Need organic modifiers to elute analytes
Widely used polar S Phase
Polysiloxanes-- stable, flexible Si--O bond lead to good diffusion.
Substituted with chemical groups for selective interaction with analyte
Polymethylsiloxanes--increase efficiency in separating closely related polar
analytes
Cyanopropyl polysiloxanes-useful for compounds with COOH
3
1
Stationary phase
Columns similar to those of HPLC.
Capillary SFC organic films bonded to
capillaries.
Because SCFs have low viscosities can
use very long columns.
Get high resolution in a reasonable time.
SFC Columns
Open tubular (derived from GC)
- Large # theoretical plates (~X500)
- Easier to control pressure (low P
drop)
Packed (derived from HPLC)
- Faster analysis
- Higher flow rates
- Higher sample capacity
Packed Columns
Similar to HPLC columns (10, 5, or 3
m porous particles)
Silica based chemically bonded
phases
Typically 10 cm long X 4.6 mm i.d
Mobile Phase
Neat Fluid
CO2 low Tc, low toxicity, nonflammability
N2O high degree of nonideality,
permits high fluid density when
compressed
Isopropyl/diethyl ether separation
of polynuclear aromatics and
polymers.
Hydrocarbon limited use due to high
flammability
n-Pentane separation of oligomers
Flourocarbon low Tc, unique
selectivity for certain solutes
3
6
36
Mobile Phase
Mix Fluid: Addition of polar organic modifier
-Enhance solubility of polar analyte
-Reduce retention volume
-Eliminate strong interaction between absorptive site and polar solute
-Will modify polarity of eluent (asso. with and polarity index)
-k and affected by modifier identity and concentration
3
7
Temperature/Pressure Effects
At lower P, > T, < solubility
At higher P, > T, > solubility
-> T, Pv of solute > solute solubility
-< fluid density < solubilizing power
> T, < solvent
>P, > solvent
T (oC)
(g/cm3)
7.3
40
0.22
7.3
80
0.14
7.3
120
0.12
40
40
0.96
40
80
40
120
0.82
0.70
Solvent Programming
Programming is very useful in controlling
solvent strength.
Variations in P (density), T, and mobile
phase composition.
Density programming is most widely
used (not simple relationship, T & P).
-> density, > solubility, < retention
- Combined T & P programming to
control and thereby solubility and
diffusion
Commonly used
Transmits UV
Colourless
Odourless
Non-toxic
Relatively cheap
Suitable Tc T is generally kept ~10o
above the Tc.
Solvent Modifiers
Add organic modifiers to > solvent
strength
- methanol
- isopropanol
- dichloromethane
- THF
- acetonitrile
Detectors
Can use either GC or LC detectors with adaptations
-LC detector: in close cell, fluid maintain under pressure, but cooled liquid
-GC detector: in open cell, fluid decompressed to gas
Ambient Pressure Ionization
FID : organics
hydrogen-atmosphere FID: organometallics
thermionic detector: N, P containing compounds
ECD: Halogenated/electronegative compounds
photoionization detector: organics with less than 10.2eV ionization potential
ion mobility detector: high electron/proton affinity compounds
Optical
UVD
FT-IR
Flourescence detector
FPD (flame photometric detector): S, P containing
compounds
CD (chemiluminescence detector): S, and easily
oxidizable compounds
Element selective plasma emission detector
LSD (light scattering detector)
Vacuum
MS with (CI, EI, CE, API ionizer)
4
9
Detectors
Most any detector used in GC or
HPLC can be used.
FID and UV detectors commonly
used.
Coupled Detectors
- MS
- FTIR
Detectors
UV absorption and FID are most common
UV absorption with packed columns
FID with capillary SFC
SFC Comparison
5
2
SFC Comparison
5
4
SFC Separations
SFC is a hybrid of gas and liquid
chromatography that combines some of
the best features of each
As in HPLC, variation of the mobile phase
composition affects separation
In SFC, mobile phase affinity for the
analyte is a function of mobile phase
density
Density is controlled by controlling system
pressure
Highly polar samples are not easy to
handle (high critical parameters & high
SFC Advantages vs GC
Can analyze non-volatile, polar, or
adsorptive
solutes
without
derivatization.
Can
analyze
compounds.
thermally
labile
SFC Advantages
Provides rapid separations without the use of organic
solvents
Uses environmentally conscious technology
Faster separation process
Decrease in resistance to mass transfer in column
5
9
SFC Disadvantages
SCF is a recent chromatography technique that requires
development in the following areas:
Method development
Hardware development
Pump design
Injection methodology
Expensive technology
Pressure & Temperature
6
0
Applications
Separation of polyaromatic
hydrocarbons in coal tars
Gradient of 50
100% acrylonitrile
(CH2CHCN) over 40
minutes
SFC
A pressure ramp is
used in the solvent,
such that solvent
density rose from
0.225g/L to 0.7 g/ml
over the retention
period of 120
minutes.
Agrichemical Application
Pesticide detection
GC conditions:
15m x 200pm
Chrysene
SFC conditions:
10m x 50pm
Open tubular column
0.15 pm film thickness
CO2 100C
Density program from 0.55 to
GC
SFC
6
6
6
Journal of Chromatographic Science, Vol. 28, January 1990 7
Microsomes,
37
C, 90 min)
M5, TMZ
CMZ
Camazepam(CMZ)
Norcamazepam(NCMZ)
Temazepam(TMZ)
M4, M5, M9' metabolites
7.571
3.921
1.223
1.325
1.478
13.058
6.160
HPLC Analysis
M 4
M9'
NCMZ
0.0
Time (min)
68
15.0
liver
mAU
microsomes,
37
C, 90 min)
CMZ
SFC Analysis
Column: Lichrosphere NH 2 , 250 x 4.6 mm
Mobile phase: 13% ethanol in CO 2 for 4 min,
then 3%/min to 30%
Flow rate: 2.5 ml/min
Outlet pressure: 150 bar
Oven temperature: 30 C
Detection: 227 nm
400
350
300
M5
250
Camazepam
(CMZ)
Norcamazepam
(NCMZ)
Temazepam (TMZ)
M4, M5, M7, M9, M9' metabolites
200
150
100
M4
NCMZ
50
M9'
TMZ
M7
M9
0
1
Time (min)
69
8
M4
3.703
2.316
CMZ
2.941
M5
mAU
400
350
300
250
200
150
100
50
0
Time
Norm.
400
Spectrum of M4
Spectrum of M5
Spectrum of CMZ
350
300
250
200
150
100
50
0
200 225 250 275 300 325 350 375
Time (min)
70
CMZ
4.461
mAU
400
350
300
250
200
150
150
100
0
2.316
Time (min)
Norm.
Spectrum
Spectrum
400
350
300
CMZ
250
200
150
100
50
0
200 225 250 275 300 325 350 375
71
Tricyclic Antidepressants
6.Buclizine
7. Benactyzine
OH
CH
CH
2
C(CH )
3 3
CCOCH2CH2N(C2H 5) 2
8. Hydroxyzine
Cl
CH
9.Perphenazine
Cl
CH2CH2OCH 2CH2OH
10.Thioridazine
CH 3
CH2CH2CH2
N
N
Cl
CH2CH2OH
N
CH2CH 2
SCH 3
N
S
S
72
mAU
15
l injected)
1.
2.
3.
4.
5.
Conditions:
Column : 4.6 x 250 mm Lichrosphere Cyanopropyl (5 m)
Mobile phase: CO 2 + 10% MeOH + 0.5% Isopropylamine
Flow rate: 3 ml/min
Column temperature: 50 C
Outlet pressure: 200 bar
1
Detector: UV - 254 nm
Amitriptyline
Imipramine
Nortriptyline
Desipramine
Protriptyline
4
5
10
2
0.50
1.00
1.50
2.00
2.50
3.00
3.50
Time
4.00
4.50
5.00
5.50
6.00
(min)
10% Methanol
73
6.50
7.00
20% Methanol
25
20
Conditions:
Column : 4.6 x 250 mm Lichrosphere Cyanopropyl (5 u m)
Mobile phase: CO 2 + 20% MeOH + 0.5% Isopropylamine
Flow rate: 3 ml/min
1
Column temperature: 50 C
Outlet pressure: 200 bar
2
Detector: UV - 254 nm
15
1.
2.
3.
4.
5.
Amitriptyline
Imipramine
Nortriptyline
Desipramine
Protriptyline
10
0
0.50
1.00
1.50
2.00
Time (min)
2.50
3.00
74
3.50
Steroids
H 3C
OH
H3C
CH 3
OH
CH 3
H3C
C=O
HO
CH 3
Testosterone
Estradiol
CH 2 O H
H3C O
Progesterone
H3 C
C=O
OH
CH 3
HO
CH 2 O H
Estrone
HO
H3C
H3 C
Cortisone
C=O
OH
OH
CH 3
CH 3
OH
OH
CH 3
Hydrocortisone
HO
Estriol
CH 3
17 Methyltestosterone
75
R es p o n se
215 nm
Progesterone, Methyltestosterone, Testosterone
Estrone, Estradiol, Cortisone, Hydrocortisone,
Estriol
0.60
0.80
1.00
1.20
1.40
1.60
1.80
Time
2.00
2.20
2.40
2.60
2.80
3.00
(min)
76
3.20
3.40
Complementary techniques
1.06% -l-
High throughput
220 nm
Key Applications:
Chiral compounds
Excipients
Drugs
Drug/metabolites
carbobenzyloxy-d,l-alanine
1.76% -d4.0
4.50
5.0
5.5
Time (min)
220 nm
6.0
6.5
77
without additive
m particles
30
20
10
0
0.50 1.00 1.50 2.00 2.50 3.00 3.50 4.00 4.50 5.00 5.50 6.00 6.50 7.00 7.50
Time (min)
78
150
with additive
100
50
0.50
1.00
1.50
2.00
2.50
3.00
3.50
4.00
4.50
5.00
5.50
6.00
6.50
Time (min)
79
7.00
7.50
250
200
250x 4.6mm,10
m Chiracel OD
150
100
Rs = 3.5
50
Time(min)
80
References
8
1
Capillary SFC
Capillary SFC, when coupled with micro-scale SFE also permits the
characterization of small samples, such as portions of single seeds and
extractables from single, live insects.
82
8
2
PROBLEMS
The restrictor
can analyze high MW, non-volatile compound, higher resolution compare to GC (see slide
17)
Compare the plate number (N) between an open tubular (Ds = 1x10-6cm2/s,
dc = 50um, df = 0.25um, L = 10m, u = 5.8cm/s) and packed column (ko =
0.5, dp = 5um, L = 0.1m, u = 2.1cm/s). k=2, and Dm = 2x10-4cm2/s.
8
3
http://www.google.com/imgres?
imgurl=http://www.chem.leeds.ac.uk/People/CMR/images/scco24.jpg&imgrefurl=http://www.chem.leeds.ac.uk/People/CMR/criticalpics.ht
ml&usg=__y5nA5mu0N3cnYx3cqlUrb7dKik=&h=294&w=308&sz=54&hl=en&start=3&zoom=1&um=1&itbs=1&tbnid=chFV9_BtWriMMM:&tbnh=112&tbnw=117&prev=/im
ages%3Fq%3Dsupercritical%2Bfluid%26um%3D1%26hl%3Den%26sa%3DN%26tbs%3Disch:1
http://en.wikipedia.org/wiki/Supercritical_fluid
8
4
8
5
Supercritical Fluid
Chromatography
Combines some advantages of liquid
chromatography with the high efficiency
of gas chromatography.
Mobile Phases
The most widely used mobile phase for
supercritical-fluid chromatography is carbon
dioxide. It is an excellent solvent for a variety
of nonpolar organic molecules. In addition, it
transmits in the ultraviolet and is odorless,
nontoxic, readily available, and remarkably
inexpensive
relative
to
other
chromatographic
solvents.
Its
critical
temperature of 31oC and its pressure of 73
atm at the critical temperature permit a wide
selection of temperatures and pressures
without exceeding the operating limits of
modern
high-performance
liquid
Detectors
A major advantage of supercritical-fluid
chromatography is that the sensitive and
universal
detectors
of
gas-liquid
chromatography are applicable to this
technique as well. For example, the
convenient flame ionization detector of gasliquid chromatography can be applied by
simply allowing the supercritical carrier to
expand through a restrictor and into a
hydrogen flame, where ions formed from the
analytes are collected at biased electrodes,
giving rise to an electrical current.
Supercritical-Fluid Chromatography
versus Other Column Methods
Several physical properties of supercritical
fluids are intermediate between the properties
of gases and liquids. As a consequence, this
new type of chromatography combines some
of the characteristics of both gas and liquid
chromatography.
Thus,
like
gas
chromatography,
supercritical-fluid
chromatography is inherently faster than liquid
chromatography because of the lower
viscosity and higher diffusion rates in the
mobile phase.
Applications
It is applicable to a class of compounds that
is not readily amenable to either gas-liquid or
liquid chromatography. These compounds
include species that are nonvolatile or
thermally unstable and, in addition, contain
no chromophoric groups that can be used for
photometric detection. Separation of these
compounds is possible with supercritical-fluid
chromatography at temperatures below 100
o
C; furthermore, detection is readily carried
out by means of the highly sensitive flame
ionization detector.
CHAPTER 29
Supercritical Fluid
Chromatography
The mobile phase is a supercritical fluid
(a fluid above its critical T and critical
pressure)
Supercritical fluid properties (density,
viscosity, and refractive index) vary with
T&P
Supercritical Fluids
At temperatures and pressures above its critical
temperature and pressure (critical point), a
substance is called a supercritical fluid. The
critical temperature is the temperature above
which a distinct liquid phase cannot exist. The
vapor pressure at its critical temperature is its
critical pressure.
Where supercritical fluids exist: The forces from
the kinetic energy of the molecules exceeds the
forces from condensing influence of the
intermolecular forces, so no distinct liquid phase
Injectors
Typical HPLC design injectors for
packed columns.
Split/Splitless valve injector (0.01 to
0.05 L injections) for open tubular
columns.
Timed - split injector (0.01 to 0.05 L
injections) for open tubular columns.
Chapter 8
Chromatography with Supercritical Fluids
Solvent power
high
Trade name
Polysiloxane
R, R':
100 % methyl
95 % methyl, 5 % phenyl
94 % methyl, 1 % vinyl, 5 % phenyl
25 % cyanopropyl, 50 % methyl,
25 % phenyl
polyethylene glycol
( CH2 CH2 O )n
Application
separation according
molecular weight
to
OV-1, SE-30
OV-3, SE-52
SE-54
OV-225
Carbowax 20 M
Separation of aromatic hydrocarbons with different gases as mobile phase. Aromatic hydrocarbons: 1
= benzene; 2 = naphthalene; 3 = fluorene; 4 = anthracene;
5 = pyrene. Gases: a = carbon dioxide (CO2); b = nitrous oxide (N2O); c = propane (C3H8); d =
propylene (C3H6); Column: 30 x 4.6 mm, unmodified silica gel. Initial pressure 12 MPa; Temperature
296.15 K; Flow rate 670 cm 3/min at STP (after Pickel /23/).
Concentration
Analytical
injection
Overloading by
volume
Overloading by
concentration
Time
Capacity Ratio
k tr tm / tm nis / nim .
tm = residence time in the mobile phase
tr = retention time of the solute
k' = capacity ratio
= volumetric phase ratio Vs / Vm
Vs = the volume of the stationary phase, to,.
Vm = the volume of the mobile phase
Vs K e
k K
,
Vm
n s K e
k K e
,
nm e
Vm nm vm
and Vs ns v s and e vm / v s .
k K e
vm Vs K e vm
.
v s Vm
vs
Capacity Factors
Capacity factors of paraffines
as a function of density
(after Mollerup et al. /18/).
Chromatographic Separation
with n = number of
stages for p:
Fi
cim
Vm Vs / K i
vi n
1
exp
2n
2 n
Chromatographic Separation
Maximum of the peak:
vi n ;
V
n vi
;
Vm Vs / K i
Points of inflection:
Chromatographic Separation
Width of peak:
b 4 n.
tr i 1 / ki ni or tr i ki ni .
Number of equilibrium stages
4 tr i
.
ni
bi
Chromatographic Separation
Chromatographic Separation
Selectivity
si j ki / k j .
Resolution
Ri j
2 trj tri
bi b j
n1 / 2 sij 1 k
Rij
.
4 sij 1 k
Chromatographic Separation
sij 1 k
n 16 R
.
s 1 k
ij
2
ij
Chromatographic Separation
2
8
k
d
2 Dim
i F
Hs 2 d p
2
u,
u
1 ki Dis
Van Deemter
Chromatographic Separation
Height of theoretical stage Hs
for SFC and HPLC
for packed columns
with different particle diameters
(after Gere et al.)
Separation of Prostaglandins
Preparative separation
Influence of temperature
Upnmoor
20 MPa; mobile phase:
CO2/methanol (5.3 wt.%);
column: 125 x 4 mm;
5 m LiChrosorb Si 60.
1992
Chromatograms of fractions
Separation of Tocopherols
Separation of Tocopherols
Solutions of -tocopherol in chloroform.
Injected volume: 10 ml;
mobile phase: CO2/methanol;
15 MPa; 293 K;
column: 125 x 4 mm;
5 m LiChrosorb Si 60.
Upnmoor 1992
98
96
94
92
90
RF=0,842
88
86
84
82
Continuous Chromatography
Rotating column
Rotating ports
Desorbent D
Extract
A+ D
Feed
A+B+D
Raffinate
B+D
Zone 1
Purification of Adsorbent
Zone 2
Enrichment of A
Zone 3
Enrichment of B
Zone 4
Purification of Desorbent
Mazzotti, ETH-Z
Gottschall: PREP 95
Preparative SMB-Plant
Depta, 2000
Adsorption Isotherms
Isotherms exhibit a point of inflection for each isomer.
c(b1 2b 2c)
q qs
1 b1c b 2c 2
50
30
30
28
20
26
24
10
Measurements
0
0,0
0,2
0,4
0,6
0,8
1,0
1,2
concentration [mg/ml]
22
1,4
20
1,6
42
100
80
dq/dc
40
38
60
36
40
34
Measurements
20
0
0,0
0,5
1,0
1,5
2,0
2,5
concentration [mg/ml]
Adsorption isotherms for Phytol cis- and trans- isomer (black lines) and
derivatives (red lines). 225 bar, 40 C, 1.8 mass% isopropanol as modifier.
32
3,0
30
dq/dc
32
dq/dc
q [mgisomer/mlstationary phase]
40
44
120
dq/dc
q [mgisomer/mlstationary phase]
34
Batch-Simulations
feed concentration:
2 mg/ml
5 mg/ml
10 mg/ml
20 mg/ml
50 mg/ml
concentration [mg/ml]
1,2
1,0
0,8
0,6
0,4
0,2
0,0
SMB-Simulation
Model: equilibrium, axially dispersed plug flow with variable velocity of
mobile phase,
Pressure drop: Ergun equation,
Properties of mobile phase (CO2) calculated with equation of state.
ci
ci
ci 1 qi
u
0
u
ci
Dap 2
t
z
z
z
t
2
SMB process modeled with four key parameters: the net flow ratios mj:
Ruthven, Storti.
mzone
TMB
SMB shift
Qzone
Qsolid Qzone
t Vcolumn total
Qsolid (1 )
Vcolumn (1 total )
SMB-Simulation
SMB- SFC: Volume-flow is a function of column length.
Therefore, net flow ratios are not constant in each zone.
New parameter:
m*zone
SMB
Qzone
mobile _ phaset shift Vcolumn total
Vcolumn (1 total )
axial dispersion
36
34
36
34
operating point
32
30
28
26
24
24 25 26 27 28 29 30 31 32 33 34
32
30
28
26
24
24 25 26 27 28 29 30 31 32 33 34
Columns: 1/1/1/1;
1000 plates per column
36
34
36
34
operating point
32
30
28
26
24
24 25 26 27 28 29 30 31 32 33 34
32
30
28
26
24
24 25 26 27 28 29 30 31 32 33 34
Columns: 1/1/1/1;
1000 plates per column
35
30
30
raffinate (cisisomer) pure
25
20
20
25
30
25
20
20
25
30
m3
8
7
Run O
2,5
1 2
9
m2
10
11
Run M
Run N
2,0
1,5
1,0
0,5
0,0
0
1
Extract
Feed Raffinate
Separation of Ibuprofen
12
11
10
9
8
7
6
5
4
3
2
1
0
-10
Sim S(+)
Sim R(-)
Exp S(+)
Exp R(-)
0
0
10
20
extract
30
40
50
length [cm]
60
70
raffinate
80
concentration [g/l]
Phytol
Diterpene-alcohol,
Intermediate for vitamin E, K1
esterified lipophilic compound
of chlorophyll
CH3 H
CH3
CH3
OH
CH3
CH3
17mg pur
0,85 mg in Hexan
Conditions of separation:
240 bar, 50C,
column 4 x 250 mm packed with
LiChrospher 100 (Silica),
flow 2,56 g carbon dioxide / min,
modifier 3 wt.- % EtOH,
productivity 45 mg/(ml, h).
Verunreinigungen
Phytolisomere
144
A Mettler-Toledo Company
BERGER
SFC
HPLC
145
146
Typically supercritical fluids are used at densities ranging from 0.1 to 0.8 of
their liquid density and 100 - 1000 times greater than that of a gas at ambient
temperature.
Pressures range from 50 atm to 500 atm.
Diffusion coefficients of supercritical CO2 varies between 10-4 and 10-3 cm2s1
.
Liquids typically have diffusivities of less than 10-5 cm2s-1.
The viscosities of supercritical fluids mirror their diffusivities and are typically
10 - 100 times lower than for liquids.
147
Instrumentation
Precise temperature setting must take place in the column.
This is achieved with a thermostatted column oven as in GC.
To achieve subambient temperatures cooling with an auxiliary CO2 tank is
employed- Usually to ~ -10 to -50C.
Pressure in system must be precisely monitored since the density of the
supercritical fluid alters with the pressure and pressure differences lead directly
to a change in the capacity factors.
Higher pressure provides greater density.
This causes elution power of the mobile phase to increase and shorter retention
times are observed.
Pressure programming in SFC as a gradient in the same way we are familiar
with it for temperature in GC or the composition of the mobile phase in HPLC.
148
The range of solvating power of practical supercritical fluids for SFC is of primary
importance, and ultimately defines the limits of the application.
The solubility of the analytes typically increases with density, and a maximum rate
of increase in solubility with pressure is generally observed near the critical pressure
where the rate of the increase of density with pressure is the greatest.
Increase pressure--> Increase density---> should decrease k
Increase temperature--> Decrease density --> should increase k to a certain
temperature until other variables start playing predominant role.
149
Stationary Phases
Stationary phase can be either a packed column or be set up in a capillary.
Packed columns are typical HPLC columns
In fused silica capillaries the stationary phase is applied in the form of
siloxanes as liquids or chemically bonded to the inner wall.
The usual measurement of the capillaries are lengths of between 10 and 20 m
with inner diameter of between 0.05 and 10 mm and film densities of 0.05 to 1
m.
150
Mobile Phases
Carbon dioxide is most frequently used as the mobile phase.
Cheap, nonpoisonous, odorless and does not absorb in the UV range up to 190
nm.
The critical CO2 data are such that the temperature and the pressure can be
varied over relatively wide ranges.
Organic modifiers are often employed such as methanol, ethanol, IPA, n-propanol,
dioxane.
The addition of these modifiers however change the critical point of the system.
Typically at even low levels of organic modifier the supercritical region is traversed.
That is because the addition of the modifier shifts the critical point to higher
temperatures and pressures.
151
Detectors
FID detection
Coupling of mass spectrometry is considerably easier to achieve by
comparisons to LC and has been used.
UV, IR, Fluorescence, Flame photometric, TCD and ECD can also be
employed.
- DAD for purity assessment
- MS to verify presence of target
- NCD to quantify on nitrogen content
-FTIR
152
153
154
156
157
158
N 1 k2
R s
4 k2 1
Resolution depends on column efficiency, solute retention and selectivity.
In SFC we can vary the variables to obtain the desired resolution.
Ex. Increase the temperature will
* Decrease the CO2 density
* May increase or decrease the retention factor
* Vapor pressure of the analyte also increases
* Increases rate of diffusion (increased efficiency)
Depending on what variable/variables predominate the Rs could improve or not.
159
160
Effect of pressure
161
162
163
A Mettler-Toledo Company
Breaking the
Purification
Bottleneck
164
Breaking the
Purification
Bottleneck
165
Practical Advantages of
SFC
167
A Mettler-Toledo Company
40%
60%
0.5
1.5
2.5
3.5
4.5
4
168
min
Limits of SFC
A Mettler-Toledo Company
800 mAU
1400
Spectrum
1200
UV
Absorbance
At 240 nm
205-500 nm
1000
800
600
400
200
250
300
350
400
0.5
1.5
2.5
3.5
4
169
450
nm
Sample Matrix?
Usually solution in organic solvent
methanol or less polar allows larger
injections
can use DMSO
small (i.e., 0.5-1 L) aqueous samples
direct
often reduced sample prep because SFC is
compatible with both lipids and polar
molecules
pills dissolved with excipients, etc. present
171
extracts from natural products
tertiary
anilines
benzylamines
sulfonamides
phenylureas
sulfonylureas
triazines
carbamates
organochlorine
organophosphorus
primary amines
amines
secondary
amines
phenyl
CN
silica
NH 2
diol
SA
carbon
dioxide
CO 2 +
methanol
CO 2 + methanol
additives
173
Instrumentation
Berger Instruments dual pump SFC with extended
flow range to 10 mls/min.
Autosampler: 1,2, 4 ml or microtiter plate accessory,
partial to full loop, multiple solvent, or sample
washes, up to 2.5 ml syringe, cooling option
Diode array detector, or variable wavelength UV
Solvent switching valve, column switching valve
available
ECD, NPD, FID GC like detectors available
Full function Chemstation for instrument control, data
acquisition, data analysis, report generation
174
Breaking the
Purification
Bottleneck
175
A Mettler-Toledo Company
176
A Mettler-Toledo Company
177
Amitriptyline
Imipramine
Nortriptyline
Desipramine
Protryptyline
UV
Absorbance
At 220 nm
0.25
0.5
0.75
1.0
1.25
1.5
1.75
178 minutes
Retention Time,
min
2.0
Breaking the
Purification
Bottleneck
Pharmaceutical
Chiral Drugs
CombiChem/High Throughput Screening
Linked closely to the success of PrepSFC, SFC/MS
and quantitative detection
Petrochemical
Aromatics in Diesel Fuel
Other ASTM methods awaiting approval
179
SUPERCRITICAL FLUID
CHROMATOGRAPHY (SFC)
Critical Temp.
(oC)
31.3
132.3
374.4
240.5
193.6
Critical Press.
(atm)
72.9
111.3
226.8
78.9
36.3
Critical Dens.
(g/mL)
0.448
0.24
0.344
0.272
0.276
Nontoxic
Low TC and PC
Easily volatilized at the end of the separation, leaving solute analytes in the
gas phase for flame ionization detection
The FID does not respond to CO2, whereas the mass spec does
SCF-III
One disadvantage of SFC is that selectivity cannot be modified
in the same way as with HPLC by using gradient elution. This
is important for large, nonvolatile molecules
Applications: see Figs. 27-6, 27-7, 27-8 in Skoog, et al.
Capillary Zone Electrophoresis
Electrophoresis is a separation that is produced by differential
migration of species in an electric field
In pure electrophoresis, this is not a chromatographic separation
because no partitioning of dissolved analytes occurs between a mobile
and stationary phase
It is generally applied to ionic substances, although some new
techniques allow separation of neutral molecules by combining
electrophoresis with chromatography d e t e c t o r
H ig h V o lt a g e
S u p p ly
2 0 -3 0 k V
F u s e d S ilic a
C a p illa r y
5 0 -10 0 cm
15 -10 0 m I D
B oth b eakers
f ille d w it h a
buffer