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基于全自动化填充吸附剂微萃取与程序升温汽化-气相色谱-质谱联用测定水样中的氯苯类化合物。

Determination of chlorobenzenes in water samples based on fully automated microextraction by packed sorbent coupled with programmed temperature vaporization-gas chromatography-mass spectrometry.

机构信息

Departamento de Química Analítica, Facultade de Ciencias, Universidade da Coruña, Campus da Zapateira s/n, 15071 A, Coruña, Spain.

出版信息

Anal Bioanal Chem. 2013 Aug;405(21):6739-48. doi: 10.1007/s00216-013-7112-x. Epub 2013 Jun 19.

DOI:10.1007/s00216-013-7112-x
PMID:23780226
Abstract

A fully automated method consisting of microextraction by packed sorbent (MEPS) coupled directly to programmed temperature vaporizer-gas chromatography-mass spectrometry (PTV-GC-MS) has been developed to determine the 12 chlorobenzene congeners (chlorobenzene; 1,2-, 1,3-, and 1,4-dichlorobenzene; 1,2,3-, 1,2,4-, and 1,3,5-trichlorobenzene; 1,2,3,4-, 1,2,3,5-, and 1,2,4,5-tetrachlorobenzene; pentachlorobenzene; and hexachlorobenzene) in water samples. The effects of the variables on MEPS extraction, using a C18 sorbent, and the instrumental PTV conditions were studied. The internal standard 1,4-dichlorobenzene d4 was used as a surrogate. The proposed method afforded good reproducibility, with relative standard deviations (RSD %) lower than 12%. The limits of detection varied between 0.0003 μg L(-1) for 1,2,3,4-tetrachlorobenzene and 0.07 μg L(-1) for 1,3- and 1,4-dichlorobenzene, while those of quantification varied between 0.001 μg L(-1) and 0.2 μg L(-1) for the same compounds. Accuracy of the proposed method was confirmed by applying it to the determination of chlorobenzenes in different spiked water samples, including river, reservoir, and effluent wastewater.

摘要

一种完全自动化的方法,包括填充吸附剂的微萃取(MEPS)与程序升温汽化器-气相色谱-质谱联用(PTV-GC-MS)直接耦合,已经被开发出来用于测定 12 种氯苯同系物(氯苯;1,2-,1,3-和 1,4-二氯苯;1,2,3-,1,2,4-和 1,3,5-三氯苯;1,2,3,4-,1,2,3,5-和 1,2,4,5-四氯苯;五氯苯;和六氯苯)在水样中的含量。采用 C18 吸附剂,研究了变量对 MEPS 萃取和仪器 PTV 条件的影响。使用 1,4-二氯苯 d4 作为内标。该方法具有良好的重现性,相对标准偏差(RSD%)低于 12%。检测限在 0.0003μg L(-1)(1,2,3,4-四氯苯)到 0.07μg L(-1)(1,3-和 1,4-二氯苯)之间,定量限在 0.001μg L(-1)到 0.2μg L(-1)之间(同一化合物)。该方法的准确性通过应用于不同加标水样(包括河流、水库和废水)中氯苯的测定得到了验证。

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