Mahesh g ame

JSPM’S
CHARAK COLLEGE OF PHARMACY & RESEARCH,
GAT NO-720/1&2, WAGHOLI, PUNE-NAGAR ROAD , PUNE -412207

A SEMINAR ON INSTRUMENTATION OF
GAS CHROMATOGRAPHY

PRESENTED BY, GUIDED BY,
MISS. MAHESH GAME DR. RAJESH J. OSWAL
PROF.SANDIP KSHIRSAGAR

DEPARTMENT OF PHARMACEUTICAL CHEMISTRY

Content’s

1 Introduction
2 Carrier Gas
-Selection of Gases
-Control of Flow
-Gas Sources and Purity
3 Sample Inlets
-Syringes and Switching Valves
-Pyrolysis
4 Ovens
- Conventional Designs
Other Designs for Control of Column Temp.
5 Detectors and Data Systems
- Detectors
-Data Systems

1. Introduction:
The key parts of a gas chromatography include: a source of gas as
the mobile phase, an inlet to deliver sample to a column, the column
where separations occur, an oven as a thermostat for the column, a
detector to register the presence of a chemical in the column effluent, and
a data system to record and display the chromatogram.

The column may arguably be considered the key component of a
gas chromatograph and accordingly has been treated separately under
another heading. However, the total variance of a separation (sT) will
conform to principles of error propagation and be a sum of variances
from the injector (sI), column (sc), detector (sd), and data system (sds).
Thus, each of these components contributes to the overall
efficiency of a GC separation and merits individual attention.

# Schematic diagram of GC Instrumentation.

2. Carrier gas :
The carrier gas or mobile phase in GC is an essential, but
limiting, facet in separations. Carrier gas is the means to move
constituents of a sample through the column and yet the choice
of possible gases is restricted. Unlike liquid chromatography
(where a wide selection of mobile phase compositions may be
possible), very little can be gained in separations through
altering the mobile phase composition to influence the partition
coefficient (k) or separation factor (a) in GC.
2.1 Selection of Gases -
The choice of a practical carrier gas is simple:nitrogen or
helium. Air may be used as a carrier gas under certain
conditions with portable or on-site chromatographs but this is
uncommon with laboratory-scale instruments.
A GC separation using nitrogen at 10 cm s-1 can be
accomplished with comparable separating efficiency using
helium at 50–60 cm s-1.

2.2 Control of
flow-
When temperature is increased for a column with constant
pressure on the inlet, the average flow rate in the column will
decrease owing to increased viscosity of the gas mobile
phase in a proportional but nonlinear manner.
Under such conditions, flow rates may slow at high
temperature and both separation speed and efficiency may
suffer. Flow may be kept constant through mass flow meters
that have inlet and outlet orifices, adjustable based upon
pressure differences.Constant flow can be delivered across a
range of pressure drops that may arise due to changes in
temperature but cannot compensate for changes in
barometric pressure.
2.3 Gas sources & Purity

A common gas source for nitrogen or helium is the pressurized
cylinder or bottled gas supply, readily supplied as a steel tank with
a two-stage pressure regulator.This is still a common gas source
though gas generators for nitrogen (air and hydrogen too) can be
commercially competitive with bottled gas and have advantages in
safety.

3.Sample
Inlets:
The chromatographic process begins when sample is
introduced into the column, ideally without disrupting flows in
the column. The chromatographic results will be reproducible
in as much as this is accomplished with a minimum of
change in pressure or flow of the carrier gas or mobile phase.
3.1 Syringes and Switching Valves-
A common method for placing samples on a GC column is
to use the microliter syringe with a needle to penetrate a
plastic membrane.
Syringe injection is a convenient and generally effective
method though the thermoplastic septum develops leaks after
repeated injections. Fatigue of the plastic septum limits the
number of injections to 30 before the septum must be
replaced.

Gas samples can be injected into the column using gas-tight
syringes or using rotary gas switching valves that offer enormous
flexibility for GC instruments. Precision gas switching valves allow
a gas sample to be measured with a precise volume and
introduced into carrier gas flow without interrupting column flow.
Sample is loaded into a loop and then, with a change in the valve
position, is swept into the column under flow of the gas source.
3.2
Pyrolysis-inlet option which is now routine in certain specific
Another
applications of material sciences is that of sample pyrolysis where
solid samples are rapidly heated to a point of thermal decomposition
in a reproducible manner. At temperatures in excess of 600 °C,
substances such as natural or synthetic polymers thermally
decompose to small molecular weight, stable substances that
provide a chromatographic profile which is unique to certain
materials. Such an injector enlarges the application of GC to solid
samples that would not normally be considered suitable for GC
characterization, and pyrolysis methods have become standardized
for some applications such as assaying plastics.

4 .Ovens :
4.1 Conventional Designs-
Liquids or solids must be converted to vapor state and maintained
as a vapor throughout the GC separation. Therefore, most gas
chromatographs are equipped with ovens to keep the column at
temperatures from 40 to 350 c
. Conventional ovens, unchanged in decades, consist of a resistive
radiates into inner volume of the oven. Heat from the resistive wire
wire coil
source is spread, ideally in an even manner, throughout the oven
volume using a fan attached to an electric motor. A thermistor or
thermocouple inside the oven is part of regulating the oven
temperature via the amount of heat released by the heating
element.
4.2 Other Designs for Control of Column Temperature-
Several alternatives to conventional ovens have been devised and
may be especially helpful for short columns or instances where little
space is available for a bulky, heated air oven.

5. Detectors & Data System

1.FLAME IONIZATION DETECTOR :

2.NITROGEN PHOSPHORUS DETECTOR (NPD):

3. ELECTRON CAPTURE DETECTOR (ECD):

4.THERMAL CONDUCTIVITY DETECTOR :

5.FLAME PHOTOMETRIC DETECTOR (FPD):

6.PHOTOIONIZATION DETECTOR (PID):

7.ELMASS SPECTROMETER (MS):

8.ECTROLYTIC CONDUCTIVITY DETECTOR (ELCD):

1.FLAME IONIZATION DETECTOR (FID):

Mechanism: Compounds are burned in a hydrogen-air flame. Carbon
containing compounds produce ions that are attracted to the collector. The
number of ions hitting the collector is measured and a signal is generated.
Sensitivity: 0.1-10 ng
Linear range: 105-107
Gases: Combustion - hydrogen and air; Makeup - helium or nitrogen
Temperature: 250-300°C,and 400-450°C for high temperature
analyses.

2.NITROGEN PHOSPHORUS DETECTOR (NPD):
Mechanism: Compounds are burned in a plasma surrounding a
rubidium bead supplied with hydrogen and air. Nitrogen and phosphorous
containing compounds produce ions that are attracted to the collector. The
number of ions hitting the collector is measured and a signal is generated.
Selectivity: Nitrogen and phosphorous containing compounds
Sensitivity: 1-10 pg
Linear range: 104-10-6
Gases: Combustion - hydrogen and air; Makeup - helium
Temperature: 250-300°C

3. ELECTRON CAPTURE DETECTOR (ECD):
Mechanism: Electrons are supplied from a 63Ni foil lining the detector
cell. A current is generated in the cell. Electronegative compounds
capture electrons resulting in a reduction in the current. The amount of
current loss is indirectly measured and a signal is generated.
Selectivity: Halogens, nitrates and conjugated carbonyls
Sensitivity: 0.1-10 pg (halogenated compounds); 1-100 pg
(nitrates); 0.1-1 ng (carbonyls)
Gases: Nitrogen or argon/methane
Temperature: 300-400°C

4. PHOTOIONIZATION DETECTOR (PID):
Mechanism: Compounds eluting into a cell are bombarded with high
energy photons emitted from a lamp. Compounds with ionization
potentials below the photon energy are ionized. The resulting ions are
attracted to an electrode, measured, and a signal is generated.
Selectivity: Depends on lamp energy. Usually used for aromatics and
olefins (10 eV lamp).
Sensitivity: 25-50 pg (aromatics); 50-200 pg (olefins)
Gases: Makeup - same as the carrier gas
Temperature: 200°C

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