Matrix-enhanced degradation of p,p'-DDT during gas chromatographic analysis: A consideration
Analysis of p,p ‘-DDT in environmental samples requires monitoring the GC-derived breakdown of this insecticide, which produces p,p ‘-DDD and/or p,p ‘-DDE, both also primary environmental degradation products. A performance evaluation standard (PES) containing p,p ‘-DDT but not p,p ‘-DDD or p,p ‘-DDE can be injected at regular intervals throughout an analytical sequence to monitor GC degradation. Some U.S. EPA methods limit GC breakdown of DDT in the PES to ≤20%. GC/MS analysis of large-volume natural water samples fortified with deuterium- and 13 C-labeled p,p ‘-DDT exhibited up to 65% DDT breakdown by the GC inlet. These matrix-enhanced GC degradation amounts substantially exceeded the <20% breakdown levels indicated by bracketing injections of the PES containing unlabeled and labeled DDT. Substantial matrix-enhanced GC degradation was not observed during analysis of a limited number of fractionated bed-sediment extracts containing labeled DDT. Use of isotopically labeled DDT seems to provide an effective tool for monitoring sample-specific DDT breakdown during GC/MS analysis. However, analyte co-elutions render impractical their use in GC/ECD analysis. The oc currence of matrix-enhanced GC degradation might have important implications on data quality and the resultant interpretations of the environmental degradation of DDT and other thermolabile contaminants.