The Gas Chromatograph (GC) makes possible to separate the volatile components of a very small sample and to determine the amount of each component present. A GC consists of a flowing mobile phase, an injection port, a separation column containing stationary phase, a detector, and a data recording system. Typically samples of 1 µL or less are injected on the column. These volumes can be further reduced by using what is called a split injection system in which a controlled fraction of the injected sample is carried away by a gas stream entering the column.
Mobile phases are generally inert gases such as helium, argon or nitrogen. Injection port is maintained at a higher temperature than the boiling point of the least volatile component in the sample mixture. Separation of the components with a wide range of boiling points is accomplished by starting at a low oven temperature and increasing the temperature over time to elute the high-boiling point components. The rule of thumb is that retention times correlate with boiling points (do not expect an exact quantitative correlation). The rate at which compound move through the columns depends also on the nature of the interaction between the compound and the stationary phase. Other variables that affect this rate are column temperature and carrier gas flow rate. Based on results of your first run, you will then vary the column temperature in order to achieve good separation of the peaks in the shortest possible time.
GC columns are two designs: packed or capillary. Packed columns are typically a glass or stainless steel coil (typically 1-5 m total length and 5 mm inner diameter) that is filled with the stationary phase, or packing coated with the stationary phase. Capillary columns are a thin fused-silica (purified silicate glass) capillary (typically 10-100 m in length and 0.25 mm diameter) that has the stationary phase coated on the inner surface. Capillary columns provide much higher separation efficiency than packed columns but are more easily overloaded by too much sample.
Flame ionization detector (FID) is the most widely used detector for organic samples. FID, use an air / hydrogen flame to pyrolyze the effluent sample. The pyrolysis of the compounds in the flame creates ions. A voltage is applied across the flame and the resulting flow of ions is detected as a current. The detector shows a different response to each compound.
GC: Shimadzu GC-2014
Detector: Flame Ionization (FID)
Column: Restek column SHRXI-5MS. High Performance Fused Silica Capillary Column (non-polar 5% diphenyl 95% dimethyl-polysiloxane phase). Length = 15 m, inner diameter = 0.25 mm ID, film thickness = 0.25 µm. Typical applications: alcohols, amines, aromatic hydrocarbons,bile acids, drugs, USEPA methods, esters, fatty acids methyl esters (FAMEs), flavors and aromas, glycerides, halogenated hydrocarbons, herbicides, hydrocarbons, organic acids, oxygenates, polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBS), pesticides, phenols, polymers, solvents, steroids, sugars, sulfur compounds
Temperature: 60 to 330 °C
MRL room 1050
Shimadzu Scientific Instruments, Inc.
7102 Riverwood Drive
Columbia, Maryland 21046, USA
Shimadzu Instruments website
Instrument Information and/or Manual:
Please contact Rachel Behrens (rachel [at] mrl [dot] ucsb [dot] edu) to schedule training. Before training starts please read the MANUALS above.