Abstract
A field-amplified sample injection–capillary zone electrophoresis (FASI-CZE) method for the analysis of benzophenone (BP) UV filters in environmental water samples was developed, allowing the separation of all compounds in less than 8 min. A 9- to 25-fold sensitivity enhancement was obtained with FASI-CZE, achieving limits of detection down to 21–59 μg/L for most of the analyzed BPs, with acceptable run-to-run and day-to-day precisions (relative standard deviations lower than 17 %). In order to remove water sample salinity and to enhance FASI sensitivity, an off-line solid-phase extraction (SPE) procedure using a Strata X polymeric reversed-phase sorbent was used and afforded recoveries up to 72–90 % for most BPs. With the combination of off-line SPE and FASI-CZE, limits of detection in the range 0.06–0.6 μg/L in a river water matrix, representing a 2,400- to 6,500-fold enhancement, were obtained. Method performance was evaluated by quantifying a blank river water sample spiked at 1 μg/L. For a 95 % confidence level, no statistical differences were observed between found concentrations and spiked concentrations (probability at the confidence level, p value, of 0.60), showing that the proposed off-line SPE-FASI-CZE method is suitable for the analysis of BP UV filters in environmental water samples at low microgram per liter levels. The method was successfully applied to the analysis of BPs in river water samples collected up- and downstream of industrialized and urban areas, and in some drinking water samples.
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The authors gratefully acknowledge the financial support received from Spanish Ministry of Economy and Competitiveness under the project CTQ2012-30836, and from the Agency for Administration of University and Research Grants (Generalitat de Catalunya, Spain) under the project 2014 SGR-539.
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Purrà, M., Cinca, R., Legaz, J. et al. Solid-phase extraction and field-amplified sample injection–capillary zone electrophoresis for the analysis of benzophenone UV filters in environmental water samples. Anal Bioanal Chem 406, 6189–6202 (2014). https://doi.org/10.1007/s00216-014-8086-z
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DOI: https://doi.org/10.1007/s00216-014-8086-z