Simultaneous determination of the endocrine disrupting compounds nonylphenol, nonylphenol ethoxylates, triclosan and bisphenol A in wastewater and sewage sludge by gas chromatography-mass spectrometry

被引:287
作者
Gatidou, Georgia
Thomaidis, Nikolaos S.
Stasinakis, Athanasios S.
Lekkas, Themistokles D.
机构
[1] Univ Athens, Dept Chem, Analyt Chem Lab, GR-15771 Athens, Greece
[2] Univ Aegean, Dept Environm Studies, Water & Air Qual Lab, Myitlene 81100, Greece
关键词
wastewater analysis; sludge; endocrine disruptors; phenolic compounds; silyl derivatization; SPE;
D O I
10.1016/j.chroma.2006.10.037
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An integrated analytical method for the simultaneous determination of 4-n-nonylphenol (4-n-NP), nonylphenol monoethoxylate (NP1EO), nonylphenol diethoxylate (NP2EO), bisphenol A (BPA) and triclosan (TCS) in wastewater (dissolved and particulate phase) and sewage sludge was developed based on gas chromatography-mass spectrometry. Chromatographic analysis was achieved after derivatization with bis(trimethylsilyl)trifluoroacetamide (BSTFA). Extraction from water samples was performed by solid-phase extraction (SPE). The optimization of SPE procedure included the type of sorbent and the type of the organic solvent used for the elution. Referred to solid samples, the target compounds were extracted by sonication. In this case the optimization of the extraction procedure included the variation of the amount of the extracted biomass, the duration and the temperature of sonication and the type of the extraction organic solvent. The developed extraction procedures resulted in good repeatability and reproducibility with relative standard deviations (RSDs) less than 13% for all the tested compounds for both types of samples. Satisfactory recoveries were obtained (> 60%) for all the compounds in both liquid and solid samples, except for 4-n-NP, which gave recoveries up to 35% in wastewater samples and up to 63% in sludge samples. The limits of detection (LODs) of the target compounds varied from 0.03 (4-n-NP) to 0.41 mu g l(-1) (NP2EO) and from 0.04 (4-n-NP) to 0.96 mu g kg(-1) (NP2EO) for liquid and solid samples, respectively. The developed methods were successfully applied to the analysis of the target compounds in real samples. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:32 / 41
页数:10
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