Restek
Heimat / Ressourcen-Hub / ChromaBLOGraphy / Avoiding Split Peaks in Gas Chromatography for QuEChERS Extracts in Acetonitrile

Avoiding Split Peaks in Gas Chromatography for QuEChERS Extracts in Acetonitrile

20 Feb 2010

decorative

Acetonitrile injections don’t damage Rxi-5Sil MS GC columns. But urban legends persist, so analysts sometimes do unnecessary and laborious solvent exchanges for QuEChERS extracts.

A real problem that might warrant solvent exchange is mismatch between the polar solvent acetonitrile and non-polar pesticide GC columns (e.g. DB-5ms, Rxi-5Sil MS). Upon injection, lack of wetting leads to split GC peaks, especially severe for early eluters. Adjusting GC oven start temperatures rarely eliminates the problem.

A simple method for avoiding split GC peaks for acetonitrile extracts is to add toluene to the extract. At 50% toluene, peak splitting is gone, and sensitivity is only reduced by 2 (not even that, considering height reduction of split peaks). Even 25% toluene can eradicate peak splitting. Adding internal standard in toluene to a QuEChERS extract prior to injection is an elegant way to kill two European Starlings with one Accrington brick. And, no solvent exchange!