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固相萃取结合气相色谱-质谱法测定水中的氯化多环芳烃

Determination of chlorinated polycyclic aromatic hydrocarbons in water by solid-phase extraction coupled with gas chromatography and mass spectrometry.

作者信息

Wang Xianli, Kang Haiyan, Wu Junfeng

机构信息

School of Municipal and Environmental Engineering, Henan University of Urban Construction, Pingdingshan, China.

出版信息

J Sep Sci. 2016 May;39(9):1742-8. doi: 10.1002/jssc.201501286. Epub 2016 Apr 13.

Abstract

Given the potential risks of chlorinated polycyclic aromatic hydrocarbons, the analysis of their presence in water is very urgent. We have developed a novel procedure for determining chlorinated polycyclic aromatic hydrocarbons in water based on solid-phase extraction coupled with gas chromatography and mass spectrometry. The extraction parameters of solid-phase extraction were optimized in detail. Under the optimal conditions, the proposed method showed wide linear ranges (1.0-1000 ng/L) with correlation coefficients ranging from 0.9952 to 0.9998. The limits of detection and the limits of quantification were in the range of 0.015-0.591 and 0.045-1.502 ng/L, respectively. Recoveries ranged from 82.5 to 102.6% with relative standard deviations below 9.2%. The obtained method was applied successfully to the determination of chlorinated polycyclic aromatic hydrocarbons in real water samples. Most of the chlorinated polycyclic aromatic hydrocarbons were detected and 1-monochloropyrene was predominant in the studied water samples. This is the first report of chlorinated polycyclic aromatic hydrocarbons in water samples in China. The toxic equivalency quotients of chlorinated polycyclic aromatic hydrocarbons in the studied tap water were 9.95 ng the toxic equivalency quotient m(-3) . 9,10-Dichloroanthracene and 1-monochloropyrene accounted for the majority of the total toxic equivalency quotients of chlorinated polycyclic aromatic hydrocarbons in tap water.

摘要

鉴于氯代多环芳烃存在潜在风险,对其在水中的存在情况进行分析十分紧迫。我们开发了一种基于固相萃取结合气相色谱和质谱法测定水中氯代多环芳烃的新方法。详细优化了固相萃取的萃取参数。在最佳条件下,该方法线性范围宽(1.0 - 1000 ng/L),相关系数在0.9952至0.9998之间。检测限和定量限分别在0.015 - 0.591 ng/L和0.045 - 1.502 ng/L范围内。回收率在82.5%至102.6%之间,相对标准偏差低于9.2%。所获得的方法成功应用于实际水样中氯代多环芳烃的测定。在研究的水样中检测到了大多数氯代多环芳烃,且1 - 一氯芘占主导地位。这是中国关于水样中氯代多环芳烃的首次报道。研究的自来水中氯代多环芳烃的毒性当量商为9.95 ng毒性当量商m(-3)。9,10 - 二氯蒽和1 - 一氯芘占自来水中氯代多环芳烃总毒性当量商的大部分。

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