How does GC×GC work?
GC×GC involves two columns: a primary column that is typically 20–30 m long, and a short secondary column that is 1–5 m long. The two columns are connected with a modulator. As in one-dimensional GC, the sample is introduced into a heated port and swept through the primary column by a carrier gas.
The peaks that elute are then sampled (ideally three or four times per peak) and each fraction is re-injected as a narrow chromatographic band into the secondary column. Passage through the secondary column is quick to ensure sharp peaks and no band overlap, with elution usually taking place in under 10 seconds. Following elution from the second column, detection takes place, and the signal is processed to generate a three-dimensional ‘surface plot’ (which can alternatively be viewed as a two-dimensional ‘contour plot’).
Importantly, the primary and secondary columns used in GC×GC have different stationary phases, allowing a mixture to be separated on the basis of two different properties – typically volatility (molecular weight) and polarity. These can be set up in one of two ways:
- Normal-phase GC×GC uses a non-polar primary column and a polar secondary column, and is the standard approach for most applications.
- Reverse-phase (or inverse-phase) GC×GC uses a polar primary column and a non-polar secondary column. This setup provides better separation of analyte groupings in certain cases.