Sequential stir bar sorptive extraction for uniform enrichment of trace amounts of organic pollutants in water samples

Abstract

A novel extraction procedure for stir bar sorptive extraction (SBSE) termed sequential SBSE was developed. Compared to conventional SBSE, sequential SBSE provides more uniform enrichment over the entire polarity/volatility range for organic pollutants at ultra-trace levels in water. Sequential SBSE consists of a SBSE performed sequentially on a 5-mL sample first without modifier using one stir bar, then on the same sample after addition of 30% NaCl using a second stir bar. The first extraction with unmodified sample is mainly targeting solutes with high K ow (log K ow > 4.0), the second extraction with modified sample solution (containing 30% NaCl) is targeting solutes with low and medium K ow (log K ow < 4.0). After extraction the two stir bars are placed in a single glass desorption liner and are simultaneously desorbed. The desorbed compounds were analyzed by thermal desorption and gas chromatography–mass spectrometry (TD-GC–MS). Recovery of model compounds consisting of 80 pesticides (organochlorine, carbamate, organophosphorus, pyrethroid, and others) for sequential SBSE was evaluated as a function of log K ow (1.70–8.35). The recovery using sequential SBSE was compared with those of conventional SBSE with or without salt addition (30% NaCl). The sequential approach provided very good recovery in the range of 82–113% for most of the solutes, and recovery less than 80% for only five solutes with low K ow (log K ow < 2.5), while conventional approaches (with or without salt addition) showed less than 80% recovery for 23 and 41 solutes, respectively. The method showed good linearity ( r 2 > 0.9900) and high sensitivity (limit of detection: <10 ng L −1) for most of the model compounds even with the scan mode in the MS. The method was successfully applied to screening of pesticides at ng L −1 level in river water samples.