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电膜萃取结合基于低浓度溶剂的超声辅助乳化微萃取衍生化,用于测定氯酚类物质,并结合气相色谱-质谱法进行分析。

Electro membrane extraction followed by low-density solvent based ultrasound-assisted emulsification microextraction combined with derivatization for determining chlorophenols and analysis by gas chromatography-mass spectrometry.

机构信息

Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore 117543, Singapore.

出版信息

J Chromatogr A. 2012 Jun 22;1243:14-22. doi: 10.1016/j.chroma.2012.04.054. Epub 2012 May 1.

DOI:10.1016/j.chroma.2012.04.054
PMID:22579488
Abstract

A highly efficient and simple two-step method, electro membrane extraction (EME) followed by low-density solvent based ultrasound-assisted emulsification microextraction (EME-LDS-USAEME) combined with derivatization and analysis by gas chromatography-mass spectrometry (GC-MS), was developed for the determination of trace level chlorophenols in environmental water samples. In the first step, the analytes were extracted, under electrical potential, from the sample solution into the acceptor solution, which was held in a polypropylene membrane sheet with 1-octanol as the supported liquid membrane. The acceptor solution from the first step was then employed as the sample solution for the second step of LDS-USAEME. In this step, the target analytes were extracted into a solvent with lower density than water that was dispersed in the sample solution with the assistance of ultrasound. The extract was separated from the sample solution by centrifugation and collected as the upper layer. Finally, the extract with a derivatization reagent were injected into a GC-MS system for analysis. Six chlorophenols, 2-chlorophenol, 4-chlorophenol, 2,3-dichlorophenol, 2,4-dichlorophenol, 2,4,6-trichlorophenol and pentachlorophenol were selected here as model compounds for developing and evaluating the method. Several factors influencing the extraction and derivatization were investigated. With the EME-LDS-USAEME procedure, high enrichment factors of up to 2198 were achieved. Under the most favorable conditions, good limits of detection (down to 0.005 μg/L), linearity (from 0.05-10 to 0.2-10 μg/L, depending on the analytes), and repeatability of extraction (RSDs below 9.7%, n=5) were obtained. The proposed method was applied to determine chlorophenols in drainwater samples.

摘要

一种高效简单的两步法,电膜萃取(EME)后结合低密度溶剂超声辅助乳化微萃取(EME-LDS-USAEME),并衍生化后用气相色谱-质谱法(GC-MS)分析,用于测定环境水样中的痕量氯酚。在第一步中,在电场作用下,将分析物从样品溶液中萃取到接受溶液中,接受溶液置于 1-辛醇支撑液膜的聚丙烯膜片中。第一步的接受溶液然后用作第二步 LDS-USAEME 的样品溶液。在这一步中,目标分析物在超声辅助下被萃取到密度低于水的溶剂中,并分散在样品溶液中。萃取物通过离心与样品溶液分离并收集在上层。最后,将萃取物与衍生化试剂一起注入 GC-MS 系统进行分析。本研究选择了六种氯酚(2-氯酚、4-氯酚、2,3-二氯酚、2,4-二氯酚、2,4,6-三氯酚和五氯酚)作为模型化合物来开发和评估该方法。考察了影响萃取和衍生化的几个因素。采用 EME-LDS-USAEME 程序,可获得高达 2198 的高富集因子。在最有利的条件下,可获得良好的检测限(低至 0.005μg/L)、线性范围(取决于分析物,从 0.05-10 到 0.2-10μg/L)和萃取重复性(RSDs 低于 9.7%,n=5)。该方法用于测定污水样中的氯酚。

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