Analysis of N-nitrosamines in water by isotope dilution gas chromatography-electron ionisation tandem mass spectrometry

被引:72
作者
McDonald, James A. [1 ]
Harden, Nick B.
Nghiem, Long D. [2 ]
Khan, Stuart J. [1 ]
机构
[1] Univ New S Wales, Sch Civil & Environm Engn, UNSW Water Res Ctr, Sydney, NSW 2052, Australia
[2] Univ Wollongong, Sch Civil Min & Environm Engn, Strateg Water Infrastruct Lab, Wollongong, NSW 2522, Australia
基金
澳大利亚研究理事会;
关键词
Disinfection byproducts; Electron impact ionisation; GC-MS/MS; DISINFECTION BY-PRODUCT; DRINKING-WATER; NITROSODIMETHYLAMINE NDMA; REVERSE-OSMOSIS; PRECURSORS; SAMPLES; SEWAGE;
D O I
10.1016/j.talanta.2012.05.032
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A method has been developed for the determination of eight N-nitrosamines in drinking water and treated municipal effluent. The method uses solid phase extraction (SPE), gas chromatography (GC) and analysis by tandem mass spectrometry (MS-MS) with electron ionization (El). The target compounds are N-nitrosodimethylamine (NDMA), N-nitrosomethyethylamine (NMEA), N-nitrosodiethylamine NDEA), N-nitrosodipropylamine (NDPA), N-nitrosodi-n-butylamine (NDBuA), N-nitrosodiphenylamine (NDPhA), N-nitrosopyrrolidine (NPyr), N-nitrosopiperidine (NPip), N-nitrosomorpholine (NMorph). The use of direct isotope analogues for isotope dilution analysis of all analytes ensures accurate quantification, accounting for analytical variabilities that may occur during sample processing, extraction and instrumental analysis. Method detection levels (MDLs) were determined to describe analyte concentrations sufficient to provide a signal with 99% certainty of detection. The established MDLs for all analytes were 0.4-4 ng L-1 in a variety of aqueous matrices. Sample matrices were observed to have only a minor impact on MDLs and the method validation confirmed satisfactory method stability over intra-day and inter-day analyses of tap water and tertiary treated effluent samples. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:146 / 154
页数:9
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