Gas Chromatography

A.) Introduction:

Gas Chromatography (GC) is a chromatographic technique in which the mobile phase is a

gas.

GC is currently one of the most popular methods for separating and analyzing
compounds. This is due to its high resolution, low limits of detection, speed, accuracy and
reproducibility.

GC can be applied to the separation of any compound that is either naturally volatile (i.e.,
readily goes into the gas phase) or can be converted to a volatile derivative. This makes
GC useful in the separation of a number of small organic and inorganic compounds.

B.) Equipment:

A simple GC system consists of:

1. Gas source (with pressure and flow regulators)
2. Injector or sample application system
3. Chromatographic column (with oven for temperature control)
4. Detector & computer or recorder
A typical GC system used is shown below (a gas chromatograph)

Carrier gas: He (common), N2, H2

Pinlet 10-50 psig
Flow = 25-150 mL/min packed column
Flow = 1-25 mL/min open tubular column
Column: 2-50 m coiled stainless steel/glass/Teflon
Oven: 0-400 °C ~ average boiling point of sample
Accurate to <1 °C
Detectors: FID, TCD, ECD, (MS)
C.) Mobile Phase:

GC separates solutes based on their different interactions with the mobile and stationary
phases.
- solute’s retention is determined mostly by its vapor pressure and volatility
- solute’s retention is controlled by its interaction with the stationary phase
- gas mobile phase has much lower density
decreased chance for interacting with solute
increased chance that solid or liquid stationary phase interacts with solute

Carrier gas – main purpose of the gas in GC is to move the solutes along the column, mobile
phase is often referred to as carrier gas.

Common carrier gas: include He, Ar, H2, N2

Carrier Gas or Mobile phase does not affect solute retention, but does affect:

1.) Desired efficiency for the GC System

- low molecular weight gases (He, H2)  larger diffusion coefficients
- low molecular weight gases  faster, more efficient separations
2.) Stability of column and solutes
- H2 or O2 can react with functional groups on solutes and stationary
phase or with surfaces of the injector, connections and detector
3.) Response of the detector
- thermal conductor requires H2 or He
- other detectors require specific carrier gas
D.) Stationary Phases:

Stationary phase in GC is the main factor determining the selectivity and retention
of solutes.

There are three types of stationary phases used in GC:

Solid adsorbents
Liquids coated on solid supports
Bonded-phase supports

1.) Gas-solid chromatography (GSC)

- same material is used as both the stationary phase and support material
- common adsorbents include:
 alumina
molecular sieves (crystalline aluminosilicates [zeolites]
and clay)
 silica
 active carbon

Magnified Pores in activated carbon

Gas-solid chromatography (GSC):

advantages:
- long column lifetimes
- ability to retain and separate some compounds not easily resolved by other
GC methods
 geometrical isomers
 permanent gases

disadvantage:
- very strong retention of low volatility or polar solutes
- catalytic changes that can occur on GSC supports
- GSC supports have a range of chemical and physical environments
 different strength retention sites
 non-symmetrical peaks
 variable retention times
2.) Gas-liquid chromatography (GLC)

- stationary phase is some liquid coated on a solid support

- over 400 liquid stationary phases available for GLC
 many stationary phases are very similar in terms of their retention properties
- material range from polymers (polysiloxanes, polyesters, polyethylene glycols) to
fluorocarbons, molten salts and liquid crystals

Based on polarity, of the 400 phases available only 6-12 are needed for most separations.
The routinely recommended phases are listed below:
Chemical nature of Max. McReynolds’ constants
Name polysiloxane temp. x’ y’ z’ m’ s’
SE-30 Dimethyl 350 14 53 44 64 41

Dexsil300 Carborane-dimethyl 450 43 64 111 151 101

OV-17 50% Phenyl methyl 375 119 158 162 243 202

OV-210 50% Trifluoropropyl 270 146 238 358 468 310 Higher the number the
OV-225 25% Cyanopropyl- 250 238 369 338 492 386 higher the absorption.
25% phenyl
Silar-SCP 50% Cyanopropyl- 275 319 495 446 637 531
50% phenyl
SP-2340 75% Cyanopropyl 275 520 757 659 942 804

OV-275 Dicyanoallyl 250 629 872 763 1106 849

McReynolds’ constants based on retention of 5 standard “probe” analytes

– Benzene, n-butanol, 2-pentanone, nitropropanone, pyridine
Preparing a stationary phase for GLC:
- slurry of the desired liquid phase and solvent is made with a solid support
solid support is usually diatomaceous earth (fossilized shells of
ancient aquatic algae (diatoms), silica-based material)
- solvent is evaporated off, coating the liquid stationary phase on the support
- the resulting material is then packed into the column

disadvantage:
- liquid may slowly bleed off with time
 especially if high temperatures are used
 contribute to background
 change characteristics of the column with time
3.) Bonded-Phase Gas chromatography

- covalently attach stationary phase to the solid support material

- avoids column bleeding in GLC
- bonded phases are prepared by reacting the desired phase with the surface of a silica-
based support
reactions form an Si-O-Si bond between the stationary phase and support
or
reactions form an Si-C-C-Si bond between the stationary phase and support
- many bonded phases exist, but most separations can be formed with the following
commonly recommended bonded-phases:
 Dimethylpolysiloxane
 Methyl(phenyl)polysiloxane
 Polyethylene glycol (Carbowax 20M)
 Trifluoropropylpolysiloxane
 Cyanopropylpolysiloxane

CH3 CH3 C6H5

H H

O Si O Si O Si
HO C C O H

CH3 CH3 C6H5

n n m H H n

advantages:
- more stable than coated liquid phases
- can be placed on support with thinner and more uniform thickness than
liquid phases
E.) Support Material:

There are two main types of supports used in GC:

Packed columns
 large sample capacity
 preparative work
Capillary (open-tubular) columns
 higher efficiency
smaller sample size
 analytical applications
F.) Elution Methods:

A common problem to all chromatographic techniques is that in any one sample there may
be many solutes present, each retained by the column to a different degree:

Best separation and limits of

detection are usually
obtained with solutes with k’
values of 2-10

Difficult to find one condition

that elutes all solutes in this
k’ range  general elution
problem

Gradient elution - change column condition with time which changes retention of solutes to
overcome general elution problem
Temperature Programming – changing the temperature on the column with time to simulate
gradient elution in GC since a solute’s retention in GC is related to its volatility.

Comparison of a GC separation using isothermal conditions and

temperature programming is shown below

ISOTHERMAL
Column temp. 120oC

Programmed temp.
(30oC to 180oC) (5o/min)

Temperature programming is usually done either in a stepwise change, a linear change or a

combination of several linear changes. A single linear change or ramp is the most common
G.) GC Detectors:

The following devices are common types of GC detectors:

1. Thermal Conductivity Detector (TCD)
2. Flame Ionization Detector (FID)
3. Nitrogen-phosphorus Detector
4. Electron Capture Detector (ECD)
5. Mass Spectrometers (discussed later in the course)

The choice of detector will depend on the analyte and how the GC method is being
used (i.e., analytical or preparative scale)

1.) Thermal Conductivity Detector (TCD)

- katherometer or hot-wire detector

- first universal detector developed for GC

Process
- measures a bulk property of the mobile phase leaving the column.
- measures ability to conduct heat away from a hot-wire (i.e., thermal conductivity)
- thermal conductivity changes with presence of other components in the mobile phase
Design
- based on electronic circuit known as a Wheatstone bridge.
- circuit consists of an arrangement of four resistors with a fixed current applied to them.
- thermal conductivity changes with presence of other components in the mobile phase.
- the voltage between points (+) and (-) will be zero as long as the resistances in the
different arms of the circuit are properly balanced

-one resistor in contact with mobile

phase leaving column

-another in contact with reference

stream of pure mobile phase

as solute emerge from column:

change in thermal conductivity  change in amount of heat removed from resistor 
change in resistor’s temperature and resistance  change in voltage difference between
points (+) and (-).
Considerations
- mobile phase must have very different thermal conductivity then solutes being
separated.
- most compounds separated in GC have thermal conductivity of about 1-4X10-5.
- H2 and He are carrier gases with significantly different thermal conductivity values.
- H2 reacts with metal oxides present on the resistors, so not used

advantages:
- truly universal detector
 applicable to the detection of any compound in GC
- non-destructive
 useful for detecting compounds from preparative-scale columns
 useful in combination with other types of GC detectors

disadvantage:
- detect mobile phase impurities
- sensitive to changes in flow-rates
- limit of detection
 ~ 10-7 M
 much higher then other GC detectors
2.) Flame Ionization Detector (FID)

- most common type of GC detector

- “universal” detector capable of measuring the presence of almost any organic and many
inorganic compound

Process
- measures the production of ions when
a solute is burned in a flame.
- ions are collected at an electrode to
create a current

advantages:
- universal detector for organics
 doesn’t respond to common inorganic compounds
- mobile phase impurities not detected
- carrier gases not detected
- limit of detection: FID is 1000x better than TCD
- linear and dynamic range better than TCD
disadvantage:
- destructive detector
3.) Nitrogen-Phosphorus Detector (NPD)

- used for detecting nitrogen- or phosphorus containing compounds

- also known as alkali flame ionization detector or thermionic detector

Process
- same basic principal as FID Alkali Bead
- measures production of ions when a solute
is burned in a flame
- ions are collected at an electrode to
create a current
- contains a small amount of alkali metal
vapor in the flame
- enhances the formation of ions from
nitrogen- and phosphorus- containing compounds
3.) Nitrogen-Phosphorus Detector (NPD)

advantages:
- useful for environmental testing
 detection of organophosphate pesticides
- useful for drug analysis
 determination of amine-containing or basic drugs
- Like FID, does not detect common mobile phase impurities or carrier gases
- limit of detection: NPD is 500x better than FID in detecting nitrogen- and
phosphorus- containing compounds
- NPD more sensitive to other heterocompounds, such as sulfur-, halogen-,
and arsenic- containing molecules

disadvantage:
- destructive detector
- NPD is less sensitive to organic compounds compared to FID
4.) Electron Capture Detector (ECD)

- radiation-based detector
- selective for compounds containing electronegative atoms, such as halogens

Process
- based on the capture of electrons by
electronegative atoms in a molecule
- electrons are produced by ionization of the
carrier gas with a radioactive source
 3H or 63Ni
- in absence of solute, steady stream of
these electrons is produced
- electrons go to collector electrode where
they produce a current
- compounds with electronegative atoms
capture electrons, reducing current

advantages:
- useful for environmental testing
 detection of chlorinated pesticides or herbicides
 detection of polynuclear aromatic carcinogens
 detection of organometallic compounds
- selective for halogen- (I, Br, Cl, F), nitro-, and sulfur-containing compounds
- detects polynuclear aromatic compounds, anhydrides and conjugated
carbonyl compounds
Example 13: (a) What properties should the stationary-phase liquid for GC possess?
(b) What is the effect of stationary-phase film thickness on GC?
(c) Why are GC stationary phases often bonded and cross-linked?