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基于漂浮有机微滴固化的液相微萃取结合气相色谱-质谱联用技术的水中邻苯二甲酸酯类物质的筛查方法

Screening method for phthalate esters in water using liquid-phase microextraction based on the solidification of a floating organic microdrop combined with gas chromatography-mass spectrometry.

作者信息

Farahani Hadi, Ganjali Mohammad Reza, Dinarvand Rassoul, Norouzi Parviz

机构信息

Center of Excellence in Electrochemistry, Faculty of Chemistry, University of Tehran, P.O. Box 14155-6455, Tehran, Iran.

出版信息

Talanta. 2008 Aug 15;76(4):718-23. doi: 10.1016/j.talanta.2008.03.002. Epub 2008 Mar 13.

DOI:10.1016/j.talanta.2008.03.002
PMID:18656647
Abstract

A simple and efficient liquid-phase microextraction (LPME) technique was developed using directly suspended organic microdrop coupled with gas chromatography-mass spectrometry (GC-MS), for the extraction and the determination of phthalate esters (dimethyl phthalate, diethyl phthalate, diallyl phthalate, di-n-butyl phthalate (DnBP), benzyl butyl phthalate (BBP), dicyclohexyl phthalate and di-2-ethylhexyl phthalate (DEHP)) in water samples. Microextraction efficiency factors, such as nature and volume of the organic solvent, temperature, salt effect, stirring rate and the extraction time were investigated and optimized. Under the optimized extraction conditions (extraction solvent: 1-dodecanol; extraction temperature: 60 degrees C; microdrop volume: 7 microL; stirring rate: 750 rpm, without salt addition and extraction time: 25 min), figures of merit of the proposed method were evaluated. The values of the detection limit were in the range of 0.02-0.05 microg L(-1), while the R.S.D.% value for the analysis of 5.0 microg L(-1) of the analytes was below 7.7% (n=4). A good linearity (r(2)>/=0.9940) and a broad linear range (0.05-100 microg L(-1)) were obtained. The method exhibited enrichment factor values ranging from 307 to 412. Finally, the designed method was successfully applied for the preconcentration and determination of the studied phthalate esters in different real water samples and satisfactory results were attained.

摘要

开发了一种简单高效的液相微萃取(LPME)技术,该技术采用直接悬浮有机微滴结合气相色谱 - 质谱联用(GC - MS),用于萃取和测定水样中的邻苯二甲酸酯(邻苯二甲酸二甲酯、邻苯二甲酸二乙酯、邻苯二甲酸二烯丙酯、邻苯二甲酸二正丁酯(DnBP)、邻苯二甲酸苄基丁酯(BBP)、邻苯二甲酸二环己酯和邻苯二甲酸二(2 - 乙基己基)酯(DEHP))。研究并优化了微萃取效率因素,如有机溶剂的性质和体积、温度、盐效应、搅拌速率和萃取时间。在优化的萃取条件下(萃取溶剂:1 - 十二醇;萃取温度:60℃;微滴体积:7μL;搅拌速率:750 rpm,不添加盐,萃取时间:25分钟),对所提出方法的性能指标进行了评估。检测限的值在0.02 - 0.05μg L⁻¹范围内,而对5.0μg L⁻¹分析物的相对标准偏差(R.S.D.%)值低于7.7%(n = 4)。获得了良好的线性关系(r²≥0.9940)和较宽的线性范围(0.05 - 100μg L⁻¹)。该方法的富集因子值范围为307至412。最后,所设计的方法成功应用于不同实际水样中所研究邻苯二甲酸酯的预浓缩和测定,并获得了满意的结果。

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