Evaluation of low-cost disposable polymeric materials for sorptive extraction of organic pollutants in water samples

被引:28
作者
Prieto, Ailette [1 ,2 ,3 ]
Rodil, Rosario [4 ]
Benito Quintana, Jose [4 ]
Rodriguez, Isaac [4 ]
Cela, Rafael [4 ]
Moeder, Monika [1 ]
机构
[1] UFZ Helmholtz Ctr Environm Res, Dept Analyt Chem, D-04318 Leipzig, Germany
[2] Univ Basque Country, Dept Analyt Chem, Bilbao 48080, Spain
[3] Basque Fdn Sci, IKERBASQUE, Bilbao 48011, Spain
[4] Univ Santiago de Compostela, Dept Analyt Chem Nutr & Food Sci, IIAA Inst Food Anal & Res, Santiago De Compostela 15782, Spain
关键词
Sorptive extraction; Polyethersulphone; Organic compounds; Water samples; Large volume injection-gas chromatography-mass spectrometry; POLYPROPYLENE MICROPOROUS MEMBRANES; ASSISTED SOLVENT-EXTRACTION; THERMAL-DESORPTION; MASS-SPECTROMETRY; PHASE MICROEXTRACTION; SORBENT INTERFACE; LIQUID-CHROMATOGRAPHY; ENDOCRINE DISRUPTORS; EMERGING POLLUTANTS; SILICONE ROD;
D O I
10.1016/j.aca.2011.12.023
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The capabilities of four commercially available and low cost polymeric materials for the extraction of polar and non-polar contaminants (log K-ow = -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 (K-pw), at two different experimental conditions, was estimated for the best suited materials and compared with the theoretical octanol-water (K-ow) partition coefficients of the analytes. Polyethersulphone displayed the largest extraction yields for both polar and non-polar analytes, with higher K-pw 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. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:119 / 127
页数:9
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