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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Headspace liquid-phase microextraction of trihalomethanes in drinking water and their gas chromatographic determination
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Headspace liquid-phase microextraction of trihalomethanes in drinking water and their gas chromatographic determination

机译:饮用水中三卤甲烷的顶空液相微萃取及其气相色谱法测定

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摘要

In the present work, a novel method for the determination of trihalomethanes (THMs) such as chloroform, dichlorobromomethane, chlorodibromomethane and bromoform in drinking water has been described. It is based on coupling headspace liquid-phase microextraction (HS-LPME) with gas chromatography-electron capture detector (GC-ECD). A microdrop of organic solvent at the tip of a commercial microsyringe was used to extract analytes from aqueous samples. Three organic solvents-xylene, ethylene glycol and 1-octanol-were compared and 1-octanol was the most sensitive solvent for the analytes. Extraction conditions such as headspace volume, extraction time, stirring rate, content of NaCl and extraction temperature were found to have significant influence on extraction efficiency. The optimized conditions were 15 ml headspace volume in a 40 ml vial, 10 min extraction time and 800 rpm stirring rate at 20 ℃ with 0.3 g ml~(-1) NaCl. The linear range was 1–100 μg l~(-1) for THMs. The limits of detection (LODs) ranged from 0.15 μg l~(-1) (for dichlorobromomethane and chlorodibromomethane) to 0.4 μg l~(-1) (for chloroform); and relative standard deviations (RSD) for most of THMs at the 10 μg l~(-1) level were below 10%. Real samples collected from tap water and well water were successfully analyzed using the proposed method. The recovery of spiked water samples was from 101 to 112%.
机译:在目前的工作中,已经描述了一种测定饮用水中三卤甲烷(THMs)的新方法,例如三氯甲烷,二氯溴甲烷,氯二溴甲烷和溴仿。它基于将顶空液相微萃取(HS-LPME)与气相色谱-电子捕获检测器(GC-ECD)耦合。使用商用微注射器尖端的一滴有机溶剂从水性样品中提取分析物。比较了三种有机溶剂(二甲苯,乙二醇和1-辛醇),其中1-辛醇是分析物最敏感的溶剂。发现顶空体积,萃取时间,搅拌速率,NaCl含量和萃取温度等萃取条件对萃取效率有重要影响。最适条件为在40 ml小瓶中15 ml的顶空体积,10 min的萃取时间和在20℃下用0.3 g ml〜(-1)NaCl的800 rpm搅拌速率。 THMs的线性范围为1–100μgl〜(-1)。检出限(LODs)从0.15μgl〜(-1)(对于二氯溴甲烷和氯二溴甲烷)到0.4μgl〜(-1)(对于氯仿);在10μgl〜(-1)水平下,大多数THM的相对标准偏差(RSD)均低于10%。使用该方法成功地分析了从自来水和井水中收集的真实样品。加标水样的回收率为101%至112%。

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