gas chromatography - philadelphia university 540...gas chromatography system • gas system •...
TRANSCRIPT
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Chapter 12
Gas Chromatography
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Principles of Gas Chromatography
How does separation take place?
• Partition of molecules between a gas mobile phase
and a liquid or solid stationary phase
Separation technique • Gas is the mobile phase and liquid (GLC) or solid (GSC) is the
stationary phase
• GLC: liquid is coated on an inert solid;
separation is the result of solubility in the liquid phase
• GSC: Particulate solid like molecular sieve is the stationary
phase;
separation is the result of adsorption on the solid surface
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Uses of GC
• Separation and analysis of organic
compounds
• Testing purity of compounds
• Determine relative amounts of
components in mixtures
• Compound identification
• Isolation of pure compounds (micro
scale work)
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Advantages of the GC
• Speed: minutes or seconds
• Resolution: complex samples
• Sensitivity: 10-9 or even 10-12 g/s
• Versatility: Gases, liquids or solids (Qal & Qant)
• GLC is more common than GSC: flexibility and resolution
• Salts and other ionic compounds + high molecular weight may not be determined by the GC
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GC Process
1. Column is selected, packed with liquid phase, and installed
2. Sample injected with microliter syringe into the injection port where it is vaporized and mixed into the carrier gas stream (helium, nitrogen, argon).
3. Sample becomes partitioned between moving gas phase and stationary liquid phase.
4. The time spent by different compounds of the sample in vapor phase is a function of their vapor pressure
5. The more volatile compounds arrive at the end of the column first and pass into the detector
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Factors Affecting Separation
Boiling Points of Components in Sample
Low boiling compounds have higher vapor pressures.
Boiling point increases with increasing molecular weight
Flow Rate of Carrier Gas
Choice of Liquid Phase (Solubility in the liquid stationary phase determines the retention time in the stationary phase)
Molecular weights, functional groups, and polarities of component molecules are factors in selecting liquid phase.
Length of Column
Similar compounds require longer columns than dissimilar compounds. Isomeric mixtures often require quite long columns
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GC Instrumentation
• Carrier gas
• Sample Injector
• Column
• Detector
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Filters/Traps
Air
Hyd
rog
en
Ga
s C
arrie
r
Column
Gas Chromatography System
• gas system
• inlet
• column
• detector
• data system
Data system
Syringe/Sampler
Inlets
Detectors
Regulators
H
RESET
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Carrier Gas System
• Carrier gases, must be chemically inert,
• Include helium, argon, nitrogen, carbon dioxide, and hydrogen.
• The choice of gases is often dictated by the detector used.
• Associated with the gas supply are pressure regulators, gauges, and flow meters.
• The carrier gas system often contains a molecular
sieve to remove water or other impurities. • Detector gases - none or air/H2 (Flame ionization
detector)
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Common Carrier Gases
• N2: Low cost, safe, simple purification
higher molecular weight. But low
thermal conductivity
• H2: High thermal conductivity, low viscosity
(low pressure drop in the column), low
cost. But more diffusion of solutes;
danger of explosion on leakage
• He: Combines advantages of N2 and H2. But
high price
• Ar: Important for ionization detector,
relatively low cost, simple purification
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Purpose of Carrier gases
1. Carrying the volatile components
through the column
2. Providing a suitable matrix for the
detector to measure the sample
components
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Requirements of a Carrier Gas
• Should be inert at the temperature used
• Pure and dry
• Should be compatible (appropriate) with the
detector
• Most common gas is He that is most useful
for TCD but greater floe rates are required to
reduce diffusion and peak broadening
• H2 is hazardous and chemically reactive
toward reducible and unsaturated samples
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Purity of Carrier Gases
• Impurities (particularly O2 & H2O) can chemically change the liquid phase and thus the tR and reduce the lifetime of the column. False peaks may appear
• Liquid stationary phases (polyesters, polysiloxanes, polyamides) degrade by O2 & H2O
• Contaminant from column may desorb in
H2O causing a high detector background
(baseline drift and noise)
• Traces of hydrocarbons cause a high background in the FID
• Purity should be >99.995%
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Drying of Carrier Gas
• Molecular sieve trap between cylinder
and column is used to remove H2O and
hydrocarbons
• Sieve should be regenerated after each
gas cylinder by heating at 300oC for 3hr
with slow flow of N2 or H2
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Two stage pressure regulator
1. It indicates the pressure left in the cylinder (min. 40 psi)
2. It indicates the increasing pressure delivered to the GC
(min. = 20 psi)
Carrier gas: He; N2; H2; Ar
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Flow control of the carrier gas
1. Effect on column efficiency
Too slow: peak broadening
Too fast: prevents good partitioning
1/8” (3 mm) O.D packed columns: 25-30 ml/min
Capillary columns: 0.01” (0.25 mm) O.D: 0.74 ml/min
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2. Effect on tR
1% change in the flow rate causes a 1% change
in tR
3. Effect on the detector response
It causes a displacement of the baseline making
quantitative analysis difficult
• For 1% accuracy in quant. Analysis fluctuation
in flow rate should not be more than ± 0.2%
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• Flow rates are normally controlled by a two-
stage pressure regulator at the gas cylinder
and some sort of pressure regulator or flow
regulator mounted in the chromatograph
• Inlet pressures usually range from 10 to 50
psi, which lead to flow rates of 25 to 150
mL/min with packed columns and 1 to 25
mL/min for open-tubular columns
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How a constant flow rate can be assured?
1. Control of carrier gas inlet pressure
2. Control of carrier gas flow rate
• In isothermal operation regulating one of them keeps
the other constant
• In programmed temperature operation, if the inlet
pressure is constant the flow rate will change with
temp.
Thus flow rate must be controlled by using
“Differential Flow Controller”
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Variation of flow rate through a column as a function of
temp. at constant inlet pressure (13.9 psig)
Column Temp Measured flow rate
relative to flow at 50oC
(Cm3/min)
50 40.0
100 34.4
150 29.6
200 27.8
250 25.6
300 20.4
Flow rate decreases due to
•The increased viscosity of the carrier gas
•Thermal expansion of liquid phase
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Effect of the Differential Flow Controller
• It assures constant mass flow rate independent of
column resistance
• Stable flow rates can be obtained over a wide range
of temperatures
Results of differential flow controller
Column Temp, Inlet Pressure He flow
oC Cm Hg ml/min
20 26.3 60.7
50 27.9 61.5
100 32.4 60.5
150 35.0 60.6
200 41.2 60.7
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Injection port
Function
• Introduce sample
• Vaporize sample
• Split sample
Main Components
It is a metal block containing:
•Heaters
•Temperature sensors
•Septum holder on the front
•Connection for the column on the rear
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Injection Methods
1. Injection ports
2. Sampling loops/valves
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Various Types of Injection ports
• Split - only a portion of injection
goes on column
• Splitless - “all” material injected
goes on column
• On-Column - cold injection (sensitive
materials)
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most common method of injection
• It involves the use of a micro-syringe to
inject a liquid or gaseous sample
through a silicone rubber diaphragm or
septum into a flash vaporizer port
located at the head of the column.
• Tinjector >50oC above the column temperature
• Septum must be stable at the Tinjector
(Flash Vaporization Inlet)
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• Rubber septum serves for about 30 injections in
ordinary care
• 5-10 injections in case of large syringes
Heated
Metal
Block
Injection
Port
liner
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Injection of liquid sample
• 10 µl syringe is the most popular device
• Load the desired volume of liquid, then draw the plunger back to pull the liquid out of the needle
• Insert the needle quickly through the septum as far as it will go
• Depress the plunger and immediately remove the needle from the injection port
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• Introducing the sample instantaneously
will avoid “appreciable spreading of the
solute band”
• 10 µl benzene sample 2 ml vapor
• 2ml vapor with 60 ml/min requires 2 sec
i.e., Injection technique would add a
peak width of at least 2 sec.
Larger samples cause broader profiles
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• For best peak shape and maximum resolution the smallest
possible sample size should be used
• More components in the sample use larger sample size
• Trace analysis use larger sample size
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Gas samples
• Special gas-tight syringes with sealing rings
around the tip of the plunger.
• The syringes have a Teflon plunger which
can form a very high seal around the glass.
• Gas sample valves
Valves may be heated if sample is
absorbed or condensed when the valve is
cold
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Solid samples
• Sealed glass or indium tube containing the sample is placed in the heated area of the injection port
• When the plunger pushes the tube into the heated area, the sealed tube melts and the volatile components flash off and are carried out into the column
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Purpose of Split Injection
• Rapid vaporization and a short retention time in the liner results in a small injection plug.
• Splitting reduces the size of the sample to an amount compatible with the sample capacity of the capillary column.
• In high resolution capillary chromatography where columns with inner diameters below 100 m are used, split ratios can exceed 1:1000.
• When the split ratio is too low, a broad injection band will be introduced into the column, resulting in broader peaks.
• Column overloading can take place. This usually results in asymmetrical peaks (peaks with leading fronts).
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Split mode
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Split liner
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Disadvantages of Split Injection
• Due to a large loss of sample, split injection is not suitable for trace analysis.
• Depending on the inlet temperature, thermal degradation can also take place, especially when using liners containing a glass frit or packed with glass wool. This means that split injection is not suited for the analysis of components prone to thermal degradation.
• Discrimination is also possible. In the heated liner, additional vaporization of the more volatile sample constituents from the needle cannot be avoided. Hence, the composition of the sample that enters the column is no longer representative of the original sample.
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• The reproducibility of split injection is strongly dependent on the geometry of the liner and the injection technique.
• The build up of non-volatile residues on the glass liner may lead to additional decomposition and adsorption problems
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Liner overload
This
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Purpose of Split Injection
• Rapid vaporization and a short retention time in the liner results in a small injection plug.
• Splitting reduces the size of the sample to an amount compatible with the sample capacity of the capillary column.
• In high resolution capillary chromatography where columns with inner diameters below 100 m are used, split ratios can exceed 1:1000.
• When the split ratio is too low, a broad injection band will be introduced into the column, resulting in broader peaks.
• Column overloading can take place. This usually results in asymmetrical peaks (peaks with leading fronts).
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Split mode
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Split liner
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Disadvantages of Split Injection
• Due to a large loss of sample, split injection is not suitable for trace analysis.
• Depending on the inlet temperature, thermal degradation can also take place, especially when using liners containing a glass frit or packed with glass wool. This means that split injection is not suited for the analysis of components prone to thermal degradation.
• Discrimination is also possible. In the heated liner, additional vaporization of the more volatile sample constituents from the needle cannot be avoided. Hence, the composition of the sample that enters the column is no longer representative of the original sample.
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• The reproducibility of split injection is strongly dependent on the geometry of the liner and the injection technique.
• The build up of non-volatile residues on the glass liner may lead to additional decomposition and adsorption problems
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Liner overload
This
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Pyrolysis Chromatography
• It is used for nonvolatile samples (e.g., Plastics)
• The sample is heated rapidly above its decomposition
temp.
• A group of volatile decomposition products will be
produced
• The products can be chromatographed to yield a
fingerprint which is characteristic of the original
material
• Pyrolyzers are attachments to the standard injection
port with a probe extending into the heated zone
• Separate pyrolyzing chamber with a transfer line to
carry the volatile products into the chromatograph
• Pyrolysis remains a rather empirical technique and
• each unit should have its own fingerprint library
determined by running samples of known composition
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On Column Injection
• It is used for samples (biological) that decompose, rearrange, or be adsorbed if they contact the heated metal surface of the port
• The needle extends directly into the column (the end of the needle penetrates the packing; this may cause damage to the needle)
• Packing length is adjusted so that the end of the needle is either or just ahead of the glass wool plug
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(Sampling Valves)
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•Valves give better reproducibility
•Require less skill
•Can be easily automated
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Injection valve
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Injection Port Temperature
• The temp. should be 20-30 oC hotter than the boiling point of the least volatile component
But low enough to prevent sample decomposition and septum bleed
• Temp. may be checked by raising it and watching :
Position, or area, or shape of the peaks. Drastic changes mean the temp. setting is high
• It should be 10% above that of the column to ensure rapid volatilization of the sample. The efficiency of the column is almost constant under this condition
• Components may be vaporized at a temp. ~100oC below its atmospheric boiling point
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• Very high boiling point or temp. sensitive material can be handled by dilution with volatile solvent that permits lowering the injection temp.
This will lower the sensitivity!
• Try various temperatures until peak broadening becomes apparent
• With temp. programming techniques low injection temps become very practical. No rush to vaporize the high boiling components
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Effect of injection port temperature on resolution
a: Methanol; b: Ethanol; c: ispropanol
Boling points: 65 – 82 oC
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Problems arising with the injection port
• Cleanliness
• Septums
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Cleanliness of the injection port
• Any material collects inside the port may trap
the sample, decompose and release
unwanted components to the column
• A glass wool plug inserted in the vaporizer
section will trap most of this material and
can be removed periodically
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Mechanical Problems
• Over tightening creates problems:
It may become impossible to push the needle
through it
It may block the carrier gas flow
• It is best to tighten the retainer by hand
• Repeated puncturing of the septum will destroy its
mechanical strength and cause leakage.
tR becomes longer and sensitivity decreases
• Change the septum regularly, preferably at the end
of the day (any air entered can be swept overnight)
Septums
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Chemical Problems
• Silicon rubber septums may adsorb some of the
sample causing: peak broadening and baseline
noise. Good injection technique and proper port
design overcome this problem
• Ports are designed for full insertion of a 2 inch
hypodermic needle; otherwise some material will
deposit on the septum and gradually releases
• The syringe plunger should be drawn after loading;
this leaves the needle filled with air and the liquid
not forced out by expansion when the needle enters
hot septum
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Thermal Problems
• Low molecular weight components in the
septum may be driven off when the septum
is first heated causing ghost peaks
especially in the case of the temperature
programming
• Conditioning is necessary
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Gas Chromatographic Columns
1. Packed Columns for GLC
2. Packed Columns for GSC
3. Capillary Columns
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Types of column • Preparative
>1/4"
>3 m in length
• Conventional
1/8 – 1/4" OD, stainless steel or glass
tube
2-6 m in length
• Capillary
• 0.1-0.5 mm ID
• 10-100 meters in length
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Capillary (Open tubular columns)
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Packed Columns
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Main Components of a Column
1.Column Tubing
• Packed
• OpenTubular
(Capillary)
2. Solid Support
3. Liquid or solid Stationary Phase
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Column Material
• Stainless Steel : most common.
adsorbs some Compounds particularly
polar ones & especially water.
• Copper tubing reacts with : amines,
acetylenes, terpens & steroids
Widely used. It is good for trace water
analysis.
• Copper oxide coating is reactive and
can interfere in gas analysis.
• O2 must be excluded from the carrier gas
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• Al is used but troublemaker due to reactive
Al-oxide formation
• Plastics: are limited due to permeability &
temperature limit
(used for reactive or highly corrosive chemicals
H2S, HF
• Teflon, polypropylene and nylon tubing are
available.
• Glass:
If glass were not difficult to form into columns &
relatively fragile it would be the very best
choice for tubing ( used for pesticides &
steroid).
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Column Size Column Length
It is the shortest length that will give the required
separation
Advantages of Short Columns: • Shorter analysis time
• lower Column temp
• Longer column life time
• Lower noise & drift due to column bleed
• Ability to resolve peaks
i.e. increasing length is not a very effective way to
increase resolution.
• Larger samples may be injected into longer columns.
L
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• Increase in Column diameter
cusses:
* increase in capacity
* decrease in column efficiency
* longer tR
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Solid Support (Stationary Phase Support)
Characteristics of Good Solid Support
• Large surface area – 1-20 m2/g
• Uniform pore diameter – 10 m or less
• Inertness (no chemical activity, Catalytically inactive)
• Regularly shaped particles
• Mechanical strength (Coating without breaking)
• Thermally stable Diatomaceous earth is the most
common (nearly, all silica).
• When diatomite supports are unsuitable, Glass or
Polymer beads are used
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Chromosorb Supports Chromosorb P
• Derived from raw diatomite
• Calcined
• Pink
• Hard
• Separate hydrocarbons; not good for polar compounds
• Most adsorptive surface, strong, efficient
Chromosorb W
• Chromosorb P flux calcined with Na2Co3
• Processed from Celite diatomaceous silica
• White
• Friable
• Separate polar compounds
• Non-adsorptive surface, most inert solid support
But fragile
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Adsorption on Column Packings
(or Capillary Walls)
• Polar analyte species such as, Alcohols
or Aromatic hydrocarbons are
adsorbed physically on the silicate
surfaces.
• Adsorption results in distorted peaks
broadened with tail
• This catalytic activity may lead to
sample decomposition
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Reasons for adsorption activity
• Silicates + Water Silanol
groups on the silicate surface
SiO
OHOH
Si
O
OH
Si
O
OH
Si
• Si-OH groups have strong affinity for polar
organic molecules
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Treatment of Solid Supports
• Non-acid washed (NAW) – an untreated form
• Acid washed (AW) – use HCl – Removes metals, impurities, Reduces surface activity and absorption
• Acid washed – Dimethyldichlorosilane treated (AW-DMCS)
Si
OH
+ (CH3)2SiCl2
HClSi
OSi CH3
CH3OH HCl
Cl
CH3
CH3
Si
OSi
CH3
CH3
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Factors upon which the solid support is chosen
1. Nature of the sample
• Acidic Sample acidic support * Non polar compounds Chromosorb-P * Compounds with Treated support polar functional is necessary groups (W&G; HP)
• Injection of water or acids may ruin many good
silinized columns. They hydrolyze the silyle ether groups
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2. Nature of Liquid Phase
• Avoid incompatibility between the
support and the liquid phase
3. Intended use for specific need (tailored
closely) or general purpose use
(better grade)
4. Coast
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Alternative Solide supports
1. Synthetic silica – based supports
(Volaspher and Quartz), Merck
* For non polar or weakly polar stationary phases. * High mechanical strength, * Uniform pore structure (thin film is possible) * The column will be packed very densely * very pure ( 99 % silicic acid) * > 95% silicic acid in diatomites.) * This material is close to the ideal supports. * It may replace Diatomites for sophisticated analysis.
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2. Silica Gel * The fine pores were widened yielding a more uniform
pore size distribution and decreasing the surface area.
* The undesirable adsorption contribution is significant.
3. Micro Glass Beads and Porous Layer
• (Glass beads coated with a thin layer of porous silica) Corning Code 0201 (DMCS) Corning Glass Works USA Glass Beads (DMCS) Applied Science Lab USA Anaport Glass Beads Analabs USA Glass Beads Perkin Elmer USA Howlett – Packard USA Zipax CSP (Porous) Du Pont USA Liqu-Chrom ASL USA Prisorb B Merck Jascosil WG03 Jasco, Japan * Glass beads with liquid phase chemically bonded are also
available
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4. Fluoro carbon Supports * extremely inert * For separation of strongly polar or reactive compounds * Excellent for water and corrosive chemicals * Most of these are made of : Teflon-6 powder : Poly(tetrafluoroethylene) resin
• PTFE supports are : soft, liable to electrostatic charge causing them to aggregate and adhere to the walls & accessories
• “This is solved by cooling to 0oC before handling”
• PTFE’s have great thermal resistance & high resistance
to chemical attack. Teflon –6 Du Pont Chromosorb T Johns Manville USA Haloport – F Howlett – Packard USA Shi malite F Shimadzu, Japan
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Stationary
Liquid Phase
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Function of Stationary Liquid Phase
• The stationary phase should provide separation of the sample with a reasonable column life
• Suitable phase is chosen on the basis of : Experience or Experiment.
• It is desirable to have maximum information
about the sample composition : bp.range,
components expected & their structure
• Stationary phases should have similar chemical structure to the sample components
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Criteria for Liquid Phases
1. Maximize differential solubility
2. High absolute solubility for sample (measure as tR)
• Solubility good but not too good.
• (Gas phase is inert & separation occurs only in Liquid Phase).
3. Thermal stability (Temp. Limitations)
(Maximum & Minimum temp.)
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4. Chemical inertness towards ample
components at temp. of operation
5. Strong attachment to the Solid Support.
6. Low vapor pressure at the temperature used
(otherwise it will bleed off the column).
7. Reproducibility, availability, cost.
– Same liquid phase produces same results when
bought from any source or from same source
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Commonly Used Liquid Phases
PHASE TEM. LIMITS Good for
1. SQUALANE 0/125oC Nonpolar
2. OV-1, SE-30 100/350 oC
3. DEXSIL-300 50/350 oC
(Most thermally stable)
4. OV-17; SP-2250 0-350 Moderately polar
5. QF-1; OV-210; 0-275
SP-2401
6. CARBOWAX-20M 60/225 Strongle polar
7. DEGS 20/200
8. OV-275 20/250
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Squalane
• Saturated, highly branches, C-30 hydrocarbon
• Non-polar
• Limited temperature range: 0-125 oC
• Separate hydrocarbons
• Standard reference for Rohrschneider and
• McReynolds constants
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• Non-polar
• Temperature range: 100-350oC
• Most widely used liquid phase
• Separate all sample types
OV-1 (SE-30) AND SP-2100
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OV-17 (SP-2250)
• 50% methyl, 50% phenylpolysiloxane
• Semi-polar
• Temperature range : 0-350oC
• Widely used to separate drugs,
steroids, carbohydrates
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Carbowax 20-M
HO – ( - CH2 – CH2 – O-)n – H
• Polymeric polyethylene glycol
• Polar
• Temperature range : 60-225oC
• Widely used for polar samples
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Liquid Phase Selection
1. Intuitive 2. Scientific
Intuition
• Liquid stationary phase separates essentially by boiling point within functional group categories.
e.g. :Silicon or squalene (non polar) separates
n-hydro carbons; and alcohols on b.p. basis.
• How does the separation take place when We have a mixture of polar and non polar Components? On b.p. basis?
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Scientific
• When more than 3 or 4 components of various properties are to be separated, the intuition does not work.
• What is the solution?
• Retention Index ( Kovats Index)
• e.g., a sample containing the following components
Compound b.p. Chemical type
Carbon tetrachloride 76oC Chlorinated hydrocarbon
Benzene 80 oC Aromatic hydrocarbon
Cyclohexane 81 oC Saturated hydrocarbon
n-Butanol 118 oC Alcohol
Available Columns • SE-30 non-polar Silicon
• Apiezon L non-polar hydrocarbon
• QF-1 Polar fluorinated silicon
• Carbowax Polar polyether
20M
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Retention Index (120 oC )ON
Compound SE-30 Apizon QF-1 Carbowax 20M
CCl4 680 687 733 895
678 683 780 961
677 691 701 756
CH3CH2CH2OH
676 620 821 1111
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• How can we deal with a list of > 300 liquid phases?
• How the duplication can be eliminated?
* Liquid phases have been classified in
terms of their separating power
* A set of reference compounds have been
used to determine how much longer the
reference compound is retained by the
liquid phase being tested than by some
standard liquid phase.
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• McRynolds constants used to
1. Show the increasing polarity of liquid phases.
2. find identical liquid phases.
* Kovats Retention Index (R.I) has been developed
as a means for qualitative analysis
• Further, the concept has been modified into a means of classifying polarities of liquid phases.
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Parameters Affect Separation Efficiency
• Solid support particle diameter
• Column length
• Column diameter
• Flow rate
• Type of carrier gas
• Pressure
• Type of liquid phase
• Amount of liquid phase
• Column tubing
• Temperature programming and isothermal column temperature
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Column Temperature
1. As the Column temp. increases a sample component spends more time in the mobile phase.
* This will cause a decrease in the tR (Faster separation)
* tR doubles for every 30oC decrease.
2. Increasing the temp. decreases the band broadening since it
leads to a decrease in the available time for diffusion in the
column.
3. The lower the temperature the better is the separation
* The column temp. should not be less than about 10oC below
the bp of the highest-boiling sample component (other wise
distorted peaks may result).
* Roughly, a temp. equal or slightly above the average b.p of a
sample results in a reasonable elution time (20 to 30 min.).
4. Optimum column temp. depends upon:
b.p. of the sample
Degree of separation required.
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Temperature Programming
1. Isothermal separation
The temperature is held constant
during the analysis
2. Programmed temperature separation
The temperature is varied gradually
according to a set program
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Column Temperature Effect (Isothermal Analysis)
Isothermal chromatographic analysis is one which is performed
at a constant column temperature.
• Higher temp. enables
rapid analysis but loss
in resolution.
• Lower temp. achieves
better resolution but
longer analysis time
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Narrow Boiling Range Samples
• Isothermal column temperature should be used.
• Select temperature 20-50oC lower than boiling range of sample when thin films are handled.
• Use highest temperature that still allows adequate resolution and stability to shorten analysis time.
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Temperature Programming
• Within a homologous series, retention time increases exponentially with the number of carbons
• As tR increases, band width increases and the peak height decreases, making detection almost impossible after a few peaks have eluted
• Since solubility of a gas in a liquid decreases as temperature increases, the retention of a sample component can be reduced by increasing column temperature
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Conclusion:
1. Better resolution
of earlier peaks
2. Latter peaks elute
more rapidly
3. Peak shapes are
more uniform
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Creating a temperature Program
• General steps to create a program assuming that the separation is possible:
1. Determine the initial temperature and time based on best possible separation of first few peaks
2. Repeat step 1 for the last few peaks to find the best final temperature and time
3. Experiment with various ramps to account for the rest of the components
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PERCENT LOADING OF STATIONARY PHASE
• How much liquid phase should be coated on the support?
• For analytical columns: 5 – 10%
• Higher loading ( up to ~ 30% ) can be applied for light gases (C1 to C4 hydrocarbons)
• Low Loading (1- 5% ) with very high boiling compounds
• The liquid phase should cover the support almost completely. If the support is inert, this condition is not a must
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Conditioning the column Why? Remove: impurities in liquid phase ; residual
solvent from coating
How?
• Install the column but do not connect to the detector
• Set the carrier flow 30 ml/min for 1/8 inch
• Heat for 1 hr at 100oC
• Raise the temperature to slightly below the b.p. of liqid phase (about 30 oC higher than expected operating column operation temp.(. Continue heating over night
• Cap the column when it is removed from the instrument
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Gas – Solid Chromatography
(Solid-Stationary Phase)
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Gas – Solid Chromatography
Basic Principle:
• Partition within the column is caused
by partial and selective adsorption on a
solid surface rather than solubility in a
liquid phase as in GLC
• “Both packed & open tubular columns
can be used”
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Characteristics & Comparison to GLC
• Higher temperatures are possible (500oC).
• No liquid stationary phase is used
• Distribution coefficients, k, are generally much larger than those for GLC. Thus separation of species that are not retained by GLC ( such as : components of air, H2S, CO, CO2 & rare gases) is possible.
• Availability of stable solid surfaces
• High column efficiencies due to no liquid phase contribution to band spreading.
• Elimination of liquid substrate bleed effect
• High flow rates & short analysis time.
• GSC, mainly, used in the analysis of extremely volatile Substances most of which are gases at room temperature
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Solid Stationary Phase
(Adsorbents)
Types of Adsorbents
• Molecular Sieves
• Silica Gel
• Alumina
• Carbosieve®
• Spherocarb®
• Carbopacks
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Molecular Sieves
• Synthetic Zeolites ( Aluminosilicates)
Al2O3 : SiO2 :H2O
• (Commercially: 3A, 4A, 5A & 13 A).
• Separation is based on the molecular size.
Molecules that have polar or polarizable
properties are adsorbed.
• They are packed easily; very durable in use;
possess high batch to batch uniformity.
• They are used for drying and purification
purposes.
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• Synthetic zeolites (alkali metal alumino-silicate)
– A12O3 . 1.92 SiO2 . X H2O
• 5A – 5A pore diameter (better resolution
• 13X – 10A pore diameter (rapid analysis)
• Surface area – 700-800 m2/g (Very large)
• Must be activated at 300oC for two hours
• Separate H2, O2, N2, CH4, CO, Ar
• CO2, H2S, SO2, Cl2, HCl are adsorbed
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Separation of light fixed gases by Molecular Sieve 5A
By time H2O will be adsorbed causing poor separation of N2 & O2
Re-activate by heating at 300oC for several hours
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CAPILLARY GC COLUMNS
(OPEN TUBULAR COLUMN GC)
( HIGH RESOLUTION GC)
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What are capillary columns?
• Long thin tube of glass, fused silica or other
material (stainless steel)
• Diameter: ~ 0.1 to 1 mm internal diameter.
• Internal diameters of ~0.05 mm are
manufactured for super critical fluid
chromatography.
• Length: 10 - 100 m. 15 to 30 m are more
common. Most of the times, we work with
columns much longer than we need.
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Capillary (Open tubular) Columns
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Capillary (Open tubular columns)
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Elution of the sample through a packed column
Eddy diffusion
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Why Capillary columns?
• The pathways through the column are practically the same length for all molecules of the sample; that is eddy diffusion is virtually ZERO and sharper peaks are expected
• Resistance to mass transfer is much smaller than the packed columns thus tR is always relatively short
• The very thin and uniform film promotes a rapid approach to equilibrium in the partition process.
• less bleed of stationary phase (thin films and low temperatures)
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• Less adsorption of trace compounds due to lower surface area compared to packed columns and deactivation process of the column surface
• Heat transfer to the column is superior to that of the large packed columns.
• Columns are very long
• Very impressive separations are obtained by these columns
• Can be used for trace analysis (subpicogram level)
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1.8 m X ¼’’(0.64 cm) packed column
152 m X 0.76 mm stainless steel OTC
50 m X 0.25 mm glass OPT
Separation of peppermint oil
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35 m X 0.35 mm glass column coated with SE 30
Isothermal at 200 oC
65 m X 0.30 mm glass column coated
with SE 32 Programmed at 100-300 oC
50 m X0.5mm stainless steel
Column coated with OV-17
Isothermal at 270 oC
22 m X 0.26 mm glass
Column coated with SE 52
Programmed at 100-260 oC
Separation of polycyclic aromatic hydrocarbons
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Separation of Styrene Impurities
Packed column, Isothermal at 95 oC,
Analysis time = 34 min, stationary phase
Was 1,2,3 tris (2-cyanoethoxy)propane
68 m X 0.28 mm OTC, isothermal at
80 oC, 7 min anaysis time. Same
stationary phase
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Capillary column gas chromatography
• The instrument should be modified to accommodate
the capillary column
• Samples injection and separation optimization
should be modified from those used for
packed columns
• Major difference from packed columns:
• Smaller ID
• Longer
• No packing
• Smaller sample capacity
• These characteristics will allow components to be
retained longer. However, the peak shape is still good
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How sensitivity is improved with capillary columns?
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TYPE OF CAPILLARY COLUMNS
1. Open Tubular Columns
A. Wall Coated Open Tubular Columns (Wcot)
• Liquid phase is deposited directly on the
glass surface without inclusion of any
additive (sometimes, microcrystalline
deposits are used)
• Columns are made of Glass or fused silica
(FSOT Columns)
• Fused silica columns possess thin walls
and they are made stronger by outside
protective polyimide coating
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Glass OT columns
Fused silica Open Tubular Columns FSOTC
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B. Supported Coated Open Tubular Columns(SCOT)
• Liquid phase is supported on a surface
covered with some type of solid support material (porous diatomaceous earth)
• Greater sample capacity compared to WCOT but less efficiency
• Coating solution contains the support powder as a suspension (one step coating)
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C. POROUS LAYER OPEN TUBULAR COLUMNS (PLOT)
• Inner surface has been extended by
substances such as fused silica, or
heavy crystalline deposits
• Porous layer is deposited followed by
coating (two steps coating)
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Typical dimensions of OTC for GC
Al-clad fused silica GC
column
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Cross sectional view of wall-coated, support coated
and porous layer columns
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Separation of a perfume oil
1.5 m X2mm packed column
30 m X 0.25 mm OTC
Carbowax 20 M stationary phase (Scale is reduced for taller peaks)
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BONDED PHASE COLUMNS
• Stationary phase is chemically bonded directly to silicon atoms on the inner surface of the walls of the column (glass or silica columns).
• Glass bonded-phase Columns: metallic sites on the surface can increase the retention of polar compounds. Metals can be removed by leaching but the glass becomes brittle.
• Fused Silica bonded-phase Columns: Fused silica is high purity glass with the composition SiO2 and characterized by high purity. They possess higher resolution and efficiency;
• Less brittle than glass: easier to handle without damage.
How the stationary phase may be bonded to the silicate surface?
Si OH + Cl Si
R
R'
R
OSi
R
R'Si
R
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Characteristics of the bonded phase columns
• Considerably higher maximum operating temperature
• Low bleed
• Much longer useful life
• By washing with an appropriate range of solvents, it is possible to recover the performance of a degraded column
• Range of Bonded-Phase Capillary Columns
• Below, several stationary phases used in bonded open tubular columns (According to J & W Scientific Products):
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Most Common GC Detectors Most common detectors roughly in order from most common
Flame Ionization Detector (FID),
•Thermal Conductivity Detector (TCD or hot wire detector),
•Electron Capture Detector (ECD),
•Photo Ionization Detector (PID),
•Flame Photometric Detector (FPD),
•Thermionic Detector
•VERY expensive choices: Atomic Emission Detector (AED)
•Ozone- or Fluorine-Induced Chemiluminescence Detectors.
•All of these (except the AED) produce an electrical signal that
varies with the amount of analyte exiting the chromatographic
column.
• Fourier Transform Infared Detector (FTIR)
• Mass Spectrometer (MS)
• Other: UV, FT-NMR
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Detector Type Support gases Selectivity Detect
ability
Dynamic
range
Flame
ionization
(FID)
Mass
flow
Hydrogen and
air Most organic cpds.
100
pg 107
Thermal
conductivity
(TCD)
Concen
-tration Reference Universal 1 ng 107
Electron
capture
(ECD)
Concen
-tration Make-up
Halides, nitrates, nitriles, peroxides,
anhydrides, organo-metallics 50 fg 105
Nitrogen-
phosphorus
Mass
flow
Hydrogen and
air Nitrogen, phosphorus 10 pg 106
Flame
photometri
c (FPD)
Mass
flow
Hydrogen and
air possibly
oxygen
Sulphur, phosphorus, tin, boron,
arsenic, germanium, selenium,
chromium
100
pg 103
Photo-
ionization
(PID)
Concen
-tration Make-up
Aliphatics, aromatics, ketones,
esters, aldehydes, amines,
heterocyclics, organosulphurs, some
organometallics
2 pg 107
Hall
electrolytic
conductivity
Mass
flow
Hydrogen,
oxygen
Halide, nitrogen, nitrosamine,
sulphur
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Schematic of a thermal
conductivity detector cell
TCD
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(TCD)
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an arrangement of two sample detector cells and two
reference detector cells.”
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• Two pairs of TCDs are used in gas chromatographs.
• One pair is placed in the column effluent to detect
the separated components as they leave the column.
• Another pair is placed before the injector or in a
separate reference column.
• The resistances of the two sets of pairs are then
arranged in a bridge circuit.
• The heated element may be a fine platinum, gold, or
tungsten wire or, alternatively, a semi conducting
thermistor.
• The resistance of the wire or thermistor gives a
measure of the thermal conductivity of the gas.
• Elutionheat lossincreased resistance needed to
balance bridge = recorded
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Characteristics of TC detector
• Specificity - very little - will detect
almost anything including H2O - called
the universal detector.
• Sensitivity to 10-7 grams/sec - this is
poor - varies with thermal condition of
the compound.
• Linear dynamic range; 104 - this is poor
- response easily becomes nonlinear.
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•sample burned in H2/air
flame
•sample must be
combustible
•must use electrometer
•flame resistance 1012W
•ppm sensitivity
•destructive
(FID)
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View of FID
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Flame Ionization Detector
Basic Principle • The effluent from the column is mixed with hydrogen
and air, and ignited.
• Organic compounds burning in the flame produce
ions and electrons which can conduct electricity
through the flame.
• A large electrical potential is applied at the burner tip,
and a collector electrode is located above the flame.
• The current resulting from the pyrolysis of any
organic compound is measured which is proportional
to the carbon content of the molecule entering.
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• FIDs are mass sensitive rather than concentration sensitive; this gives the advantage that changes in mobile phase flow rate do not affect the detector's response.
• The FID is a useful general detector for the analysis of organic compounds;
– it has high sensitivity,
– a large linear response range,
– low noise.
– robust and easy to use
– unfortunately, it *destroys the sample.
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Characteristics of a Flame Ionization Detector
(FID)
• Specificity - most organics.
• Sensitivity - 10-12 g/sec for most organics -- this is
quite good.
• Linear range 106 - 107 -- this is good.
•
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GC-MS: The equipment
Gas chromatograph –
• this is an oven that contains a 20-60 meter long capillary column (wound into a coil). The internal diameter is 0.2-0.5 mm.
• The column contains a thin film of a resin inside.
• The column is connected to a pressurized tank of an inert gas (usually helium) that creates a flow of gas through the column.
• The sample (containing a mixture of compounds) is injected at the top of the column when the temperature is low (typically between 40 and 80 C).
• The temperature is then raised and the different compounds are separated based on their volatility and their affinity for the column.
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Mass spectrometer –
• The traditional (not TOF) mass spectrometer ionizes the sample (in this case an individual compound) with the use of electrons (electron impact ionization).
• The resulting ions are then accelerated in an electric field and then subjected to a magnetic field that causes the ions to deviate from a straight course.
• The deviation is a function of the mass-to-charge (m/z) ratio.
• Many of the ions fragment upon electron impact.
• Between the m/z ratio of the molecular ion (unfragmented) and the fragmentation pattern that is observed it is possible to determine the identity of the compound that eluted off of the GC column.
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Internal Construction of a Gas Chromatograph-
Mass Spectrometer
Inject Fragment and Ionize
Separate Fragment Ions
Detect Fragment Ions
Separate Components Of the Mixture
Display Spectrum
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GC-MS: A Separation and Identification
Method
Time since injection. Separation!
Mass spectrum of each Component of the mixture. Identification!
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The data
5 10 15 20 25 30 35 40 45 50 55 60 65
2500e3
5000e3
7500e3
10.0e6
12.5e6
15.0e6
0 25 50 75 100 125 1500e3
500e3
1000e3
1500e3
2000e3
2500e3
3000e3
3500e3
4000e3
120
91
65
51
77 105144136
0 25 50 75 100 125 150 1750e3
250e3
500e3
750e3
1000e3
1250e3
1500e3
1750e3
2000e3
2250e3
2500e3 150
135
77
107
51
6389
117 166 175
chromatogram
Retention time
mass spectrum
m/z