Abstract

A method for speciation of dimethylselenide (DMeSe), dimethyldiselenide (DMeDSe) and diethylselenide (DEtSe) in sediments based on a coupling between a pervaporation module, a preconcentration sorptive trap and a gas chromatograph-mass spectrometer is reported. The coupling is performed through a high pressure injection valve which allows two different operational modes: (a) analysis without preconcentration, in which analytes are directly driven from the pervaporation chamber to the injection port of the chromatograph, and (b) analysis with preconcentration in a trap, in which the analytes from the pervaporation chamber are first trapped on a Tenax minicolumn and then thermally desorbed and driven to the GC. This second approach improves the sensitivity compared to the direct coupling, reaching estimated absolute detection limits lower than 0.6 ng Se for each tested species. The method is applied to the determination of volatile organic selenium species in several sediments collected from different areas in the Southwest of Spain.

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