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Evaluation of low-cost disposable polymeric materials for sorptive extraction of organic pollutants in water samples
Authors:Ailette Prieto  Rosario Rodil  José Benito Quintana  Isaac Rodríguez  Rafael Cela  Monika Möder
Institution:1. Department of Analytical Chemistry, University of the Basque Country, P.K. 644, 48080 Bilbao, Spain;2. IKERBASQUE, Basque Foundation for Science, 48011 Bilbao, Spain;3. Department of Analytical Chemistry, Helmholtz Centre for Environmental Research – UFZ Permoserstraße 15, D-04318 Leipzig, Germany;4. Department of Analytical Chemistry, Nutrition and Food Science, IIAA-Institute for Food Analysis and Research, University of Santiago de Compostela, 15782 Santiago de Compostela, Spain
Abstract:The capabilities of four commercially available and low cost polymeric materials for the extraction of polar and non-polar contaminants (log Kow = −0.07–6.88, from caffeine to octocrylene, respectively) from water samples was compared. Tested sorbents were polyethersulphone, polypropylene and Kevlar, compared to polydimethylsiloxane as reference material. Parameters that affect the extraction process such as pH and ionic strength of the sample, extraction time and desorption conditions were thoroughly investigated. A set of experimental partition coefficients (Kpw), at two different experimental conditions, was estimated for the best suited materials and compared with the theoretical octanol–water (Kow) partition coefficients of the analytes. Polyethersulphone displayed the largest extraction yields for both polar and non-polar analytes, with higher Kpw and lower matrix effects than polydimethylsiloxane and polypropylene. Thus, a sorptive microextraction method, followed by large volume injection (LVI) gas chromatography–tandem mass spectrometry (GC–MS/MS), was proposed using the former sorbent (2 mg) for the simultaneous determination of model compounds in water samples. Good linearity (>0.99) was obtained for most of the analytes, except in the case of 4-nonylphenol (0.9466). Precision (n = 4) at 50 and 500 ng L−1 levels was in the 2–24% and limits of detection (LODs) were in the 0.6–25 ng L−1 range for all the analytes studied.
Keywords:Sorptive extraction  Polyethersulphone  Organic compounds  Water samples  Large volume injection-gas chromatography&ndash  mass spectrometry
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