Gas chromatography is in principle similar to column chromatography (as well as other

forms of chromatography, such as HPLC,TLC), but has several notable differences. First,
the process of separating the compounds in a mixture is carried out between a liquid
stationary phase and a gas mobile phase, whereas in column chromatography the
stationary phase is a solid and the mobile phase is a liquid. (Hence the full name of the
procedure is "Gasliquid chromatography", referring to the mobile and stationary phases,
respectively.)
A gas chromatograph (GC) is an analytical instrument that measures the content of various
components in a sample. The analysis performed by a gas chromatograph is called gas
chromatography.
Principle of gas chromatography: The sample solution injected into the instrument enters a
gas stream which transports the sample into a separation tube known as the "column."
(Helium or nitrogen is used as the so-called carrier gas.) The various components are
separated inside the column. The detector measures the quantity of the components that
exit the column. To measure a sample with an unknown concentration, a standard sample
with known concentration is injected into the instrument. The standard sample peak
retention time (appearance time) and area are compared to the test sample to calculate the
concentration.

Hydrogen has the lowest viscosity of all gases, thereby provides the highest mobile
phase velocity and therefore the shortest analysis time. Helium, on the other hand,
gives the best overall performance and peak resolutions for many applications,
making it an optimum choice of carrier gas in those cases.
Gas Chromatography can be defined as differential migration processes where gases or vaporised
sample components are selectively retained by a stationary phase.

In a GC analysis, a known volume of gaseous or liquid analyte is injected into the

"entrance" (head) of the column, usually using a microsyringe (or, solid phase
microextraction fibers, or a gas source switching system). As the carrier gas sweeps the
analyte molecules through the column, this motion is inhibited by the adsorption of the
analyte molecules either onto the column walls or onto packing materials in the column. The
rate at which the molecules progress along the column depends on the strength
of adsorption, which in turn depends on the type of molecule and on the stationary phase
materials. Since each type of molecule has a different rate of progression, the various
components of the analyte mixture are separated as they progress along the column and
reach the end of the column at different times (retention time). A detector is used to monitor
the outlet stream from the column; thus, the time at which each component reaches the
outlet and the amount of that component can be determined. Generally, substances are
identified (qualitatively) by the order in which they emerge (elute) from the column and by
the retention time of the analyte in the column.