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气相色谱-质谱法同时测定废水和污水污泥中的内分泌干扰化合物壬基酚、壬基酚聚氧乙烯醚、三氯生和双酚A

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

作者信息

Gatidou Georgia, Thomaidis Nikolaos S, Stasinakis Athanasios S, Lekkas Themistokles D

机构信息

Laboratory of Analytical Chemistry, Department of Chemistry, University of Athens, Panepistimioupolis Zografou, 15771 Athens, Greece.

出版信息

J Chromatogr A. 2007 Jan 5;1138(1-2):32-41. doi: 10.1016/j.chroma.2006.10.037. Epub 2006 Oct 30.

Abstract

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 microg l(-1) (NP2EO) and from 0.04 (4-n-NP) to 0.96 microg 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.

摘要

基于气相色谱 - 质谱联用技术,开发了一种同时测定废水(溶解相和颗粒相)及污水污泥中4 - 正壬基酚(4 - n - NP)、壬基酚单乙氧基化物(NP1EO)、壬基酚二乙氧基化物(NP2EO)、双酚A(BPA)和三氯生(TCS)的综合分析方法。采用双(三甲基硅基)三氟乙酰胺(BSTFA)进行衍生化后进行色谱分析。水样通过固相萃取(SPE)进行萃取。SPE程序的优化包括吸附剂类型和用于洗脱的有机溶剂类型。对于固体样品,目标化合物通过超声提取。在这种情况下,提取程序的优化包括提取生物量的量、超声处理的持续时间和温度以及提取有机溶剂的类型。所开发的提取程序具有良好的重复性和再现性,两种类型样品中所有测试化合物的相对标准偏差(RSD)均小于13%。除4 - n - NP外,液体和固体样品中所有化合物均获得了令人满意的回收率(>60%),4 - n - NP在废水样品中的回收率高达35%,在污泥样品中的回收率高达63%。目标化合物的检测限(LOD)分别为:液体样品中从0.03(4 - n - NP)到0.41 μg l⁻¹(NP2EO),固体样品中从0.04(4 - n - NP)到0.96 μg kg⁻¹(NP2EO)。所开发的方法成功应用于实际样品中目标化合物的分析。

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