and is removed by pumps, while the larger sample molecules continue through
into the MS. A complete GC-MS system is shown in Figure 1(a). The interface
should be maintained at the temperature of the GC outlet, usually by enclosing
it in the GC oven.
Most types of mass spectrometer are suitable for GC-MS work, although
those with a quadrupole analyzer (Topic E14) are very often used because of
their ability to scan rapidly.
The chromatogram will be recorded by the GC detector and data system, but
can also be derived by continuously measuring the total ion current (TIC)for
the ions generated as a function of the elapsed time. This total ion current
chromatogram matches that from the GC detector, and may also detect other
solutes. By selecting a particular mass/charge (m/z) ratio, selected ion moni-
toring (SIM) may be used to detect a particular ion; for example, m/z320, 322
and 324 may be studied in analyzing mixed dioxins, since these ions are charac-
teristic of a particular tetrachlorodibenzo-p-dioxin. Detection down to 10–15g of
a solute is possible.Applications Both qualitative and quantitative analysis can be achieved with GC-MS and it is
now used widely on complex samples of all types.
F3 – Gas chromatography-mass spectrometry 295
Carrier
gasSampleGas
chromatographSplitterEluentOptionalChromatography
detectorVDU/computing
integratorInterface SpectrometerSpectra
stored on
computerChromatogram
generated from
spectral signals
printer(a)Fig. 1. (a) Schematic of a GC-MS system; (b) jet separator. Reproduced from F.W. Fifield
& D. Kealey, Principles and Practice of Analytical Chemistry, 5th edn, 2000, with permission
from Blackwell Science Ltd.From GC To ion sourceTo vacuum(b) To vacuum