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Today, most GC columns are fused silica capillaries with an inner diameter of 100–320 micrometres (0.0039–0.0126 in) and a length of 5–60 metres (16–197 ft). The GC column is located inside an oven where the temperature of the gas can be controlled and the effluent coming off the column is monitored by a suitable detector. [1]
A fractionating column or fractional column is equipment used in the distillation of liquid mixtures to separate the mixture into its component parts, or fractions, based on their differences in volatility. Fractionating columns are used in small-scale laboratory distillations as well as large-scale industrial distillations.
To prevent the stationary phase from leaking out of the column interior a polymer, stainless steel or ceramic net is usually applied. Depending on the application material- and size-requirements may change. Gas chromatography (GC): Older columns were made of glass or metal packed with particles of a solid stationary phase. More recently ...
Pyrolysis–gas chromatography–mass spectrometry is a method of chemical analysis in which the sample is heated to decomposition to produce smaller molecules that are separated by gas chromatography and detected using mass spectrometry. Pyrolysis is the thermal decomposition of materials in an inert atmosphere or a vacuum.
Here the distillation head and fractionating column are combined in one piece. Differential centrifugation . Fractionation is a separation process in which a certain quantity of a mixture (of gasses, solids, liquids, enzymes , or isotopes , or a suspension ) is divided during a phase transition , into a number of smaller quantities ( fractions ...
The previously described work of Martin and Synge impacted the development of the previously known column chromatography and inspired new forms of chromatography such as countercurrent distribution, [9] paper chromatography, [10] and gas-liquid chromatography which is more commonly known as gas chromatography. The modification of silica gel ...
To improve fractionation the apparatus is set up to return condensate to the column by the use of some sort of reflux splitter (reflux wire, gago, Magnetic swinging bucket, etc.) – a typical careful fractionation would employ a reflux ratio of around 4:1 (4 parts returned condensate to 1 part condensate take off).
Most commonly, the FID is attached to a gas chromatography system. The eluent exits the gas chromatography column (A) and enters the FID detector’s oven (B). The oven is needed to make sure that as soon as the eluent exits the column, it does not come out of the gaseous phase and deposit on the interface between the column and FID.