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水和污水样品中环氧氯丙烷的测定

Determination of epichlorohydrin in water and sewage samples.

作者信息

Gaca Jerzy, Wejnerowska Grazyna

机构信息

Department of Chemistry and Environmental Protection, Faculty of Chemical Technology and Engineering, University of Technology and Agriculture in Bydgoszcz, 3 Seminaryjna St., 85-326 Bydgoszcz, Poland.

出版信息

Talanta. 2006 Dec 15;70(5):1044-50. doi: 10.1016/j.talanta.2006.02.017. Epub 2006 Mar 20.

Abstract

The simple, quick and effective methods for the analysis of epichlorohydrin (ECH) in water and sewage samples with the use of gas chromatography have been presented. From among all the methods developed, the procedures for monitoring drinking-water quality and the methods which allow the determination of epichlorohydrin in sewage samples have been selected. The limits of ECH detection have been determined by direct aqueous injection (DAI) into the chromatographic column and an analysis with the application of a flame ionization detector (FID), a mass spectrometry detector (MS), an electron capture detector (ECD) and atomic emission detection (AED) detectors. The method allows the determination of ECH in water samples at the concentration level of 0.1mgl(-1). Moreover, the developed methods of water samples preparation for chromatographic analysis using the following extraction methods: headspace (HS), stripping with adsorption on solid phase, liquid-liquid extraction (LLE), solid phase extraction (SPE) and solid phase microextraction (SPME) have been evaluated. The limits of ECH detection for each procedure with the application of gas chromatography (GC) combined with various detectors have been determined and their statistical evaluation has been presented. The SPME method allowed us to determine ECH in water samples at the concentration levels of 1.0ngl(-1). The results of studies on the choice of the selective methods allowing ECH analysis in sewage samples have been demonstrated. The applied SPME method was found to be a quick and effective technique to determine micro trace amounts of ECH in samples containing high amounts of various organic compounds.

摘要

介绍了使用气相色谱法分析水和污水样品中环氧氯丙烷(ECH)的简单、快速且有效的方法。在所有已开发的方法中,选择了监测饮用水质量的程序以及可测定污水样品中环氧氯丙烷的方法。通过直接将水样注入色谱柱,并使用火焰离子化检测器(FID)、质谱检测器(MS)、电子捕获检测器(ECD)和原子发射检测(AED)检测器进行分析,确定了环氧氯丙烷的检测限。该方法能够测定浓度为0.1mg l⁻¹的水样中的环氧氯丙烷。此外,还评估了使用以下萃取方法进行色谱分析的水样制备方法:顶空(HS)、固相吸附吹扫、液液萃取(LLE)、固相萃取(SPE)和固相微萃取(SPME)。已确定了使用气相色谱(GC)结合各种检测器的每个程序的环氧氯丙烷检测限,并给出了它们的统计评估。固相微萃取方法使我们能够测定浓度为1.0ng l⁻¹的水样中的环氧氯丙烷。展示了关于选择允许分析污水样品中环氧氯丙烷的选择性方法的研究结果。发现所应用的固相微萃取方法是一种快速有效的技术,可用于测定含有大量各种有机化合物的样品中的微量环氧氯丙烷。

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