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

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. (c) 2008 Elsevier B.V. All rights reserved.