Large volume sample stacking in capillary zone electrophoresis for the monitoring of the degradation products of metribuzin in environmental samples.

A capillary zone electrophoresis (CZE) method with UV-vis detection has been developed for the simultaneous monitoring of the major degradation products of metribuzin, i.e. deaminometribuzin (DA), deaminodiketometribuzin (DADK) and diketometribuzin (DK). The dissociation acid constants have also been estimated by CE and no significant differences have been observed with the values obtained by applying other techniques. Optimum separation has been achieved in less than 9 min in 40 mM sodium tetraborate buffer, pH 9.5 by applying a voltage of 15kV at 25 degrees C and using p-aminobenzoic acid as internal standard. In order to increase sensitivity, large volume sample stacking (LVSS) with polarity switching has been applied as on-line pre-concentration methodology. Detection limits of 10, 10 and 20 ng/mL for DA, DADK and DK, respectively were obtained. The method has been applied to soil samples, after pressurized liquid extraction (PLE). Samples were extracted at high temperature (103 degrees C and 1500 psi) using methanol as extraction solvent and sodium sulphate as drying agent. This PLE procedure was followed by an off-line pre-concentration and sample clean-up procedure by solid-phase extraction (SPE) using a LiChrolut EN sorbent column. These last two procedures were also suitable for the direct treatment of groundwater samples before CE analysis. The combination of both off-line and on-line pre-concentration procedures provided a significant improvement in sensitivity. LVSS provided pre-concentration factors of 4, 36 and 28 for DK, DA and DADK, respectively and with SPE a pre-concentration of 500-fold for the case of water samples and of 2.5-fold in the case of soil samples was obtained. The method is suitable for the monitoring of these residues in environmental samples with high sensitivity, precision and satisfactory recoveries.

Gas chromatographic-mass spectrometric method for the determination of bisphenol A and its chlorinated derivatives in urban wastewater.

The simultaneous determination of trace amounts of endocrine disruptors such as bisphenol A (BPA) and its monochloro, dichloro, trichloro and tetrachloro derivatives in wastewater has been developed using gas chromatography-mass spectrometry (GC-MS). Compounds were previously extracted from the aqueous samples using a liquid-liquid extraction procedure with a mixture of dichloromethane:carbon tetrachloride (25/75). After extraction, solvent was removed and a silylation step was carried out with N,O-bis(trimethylsilyl) trifluoroacetamide (BSTFA). The silylated compounds were identified and quantified by GC-MS using an HP1-MS column. The retention times were 6.64 min for BPA silylated, 7.26 min for Cl-BPA silylated, 7.99 min for Cl(2)-BPA silylated, 8.85 min for Cl(3)-BPA silylated and 9.95 min for Cl(4)-BPA silylated. A clean-up is not necessary using SIM mode. Deuterated anthracene (2H(10)-anthracene) was used as an internal standard. The detection limits obtained were 0.3, 0.6, 2.0, 4.5 and 13.0 ng L(-1) for silylated BPA, Cl-BPA, Cl(2)-BPA, Cl(3)-BPA and Cl(4)-BPA, respectively. The proposed method was applied satisfactory to the determination of these chemicals, in different types of wastewater previously spiked with different amounts of these chemicals at concentration levels ranging from 0.01 to 2.50 microg L(-1) for BPA, 0.05-2.50 micro L(-1) for Cl-BPA and 0.05-5.00 microg L(-1) for Cl(2)-BPA, Cl(3)-BPA and Cl(4)-BPA, respectively. The method was validated following standard addition methodology.