GC Syringe
Shown here is an example of a syringe for injecting samples into a gas chromatograph. This syringe has a maximum capacity of 10 μL with graduations every 0.1 μL.
Explore resources, experiments, and teaching materials shared by the analytical sciences community.
Shown here is an example of a syringe for injecting samples into a gas chromatograph. This syringe has a maximum capacity of 10 μL with graduations every 0.1 μL.
Solid-phase microextraction (SPME) is an attractive method for isolating an analyte prior to injecting it into a gas chromatograph. In one approach, which is illustrated here, a fused-silica fiber is placed inside a […]
Shown here is an example of a packed column for gas chromatography. This column is made from stainless steel and is 2 m long with an internal diameter of 3.2 mm. The […]
Photograph showing an example of a typical gas chromatograph with insets showing the heated injection ports—note the symbol indicating that it is hot—and the oven containing the column. This particular instrument is […]
One way to improve a separation is to decrease the height of a column’s theoretical plate. The figures here consider four contributions to plate height: variations in paths length, longitudinal diffusion, mass […]
The illustration below shows how the mobile phase pH in liquid chromatography affects our ability to separate a mixture of four substituted benzoic acids. The retention times in (a) suggest there are many […]
Adjusting the retention factor to improve the resolution between one pair of solutes may lead to unacceptably long retention times for other solutes. For example, suppose we need to analyze a four-component […]
The ideal chromatographic peak has a Gaussian profile, which occurs if the solute’s partition coefficient, KD, between the stationary phase and mobile phase KD = [S]s/[S]m is independent of the solute’s concentration. If this […]
The goal of chromatography is to separate a mixture into a series of chromatographic peaks, each representing a single component of the mixture. The resolution between two chromatographic peaks, RAB, is a […]
A solute’s chromatographic peak may be characterized in many ways, two of which are shown in this figure. Retention time, tr, is the time between when we inject the sample injection and […]
The most common method for bringing the stationary phase and the mobile phases into contact is to hold the stationary phase within a column and to pass the mobile phase through the […]
In chromatography, a separation occurs because there is a difference in the equilibrium partitioning of solutes between the mobile phase and the stationary phase. Equilibrium partitioning, however, is not the only basis […]