Literature DB >> 22251887

Analysis of halonitriles in drinking water using solid-phase microextraction and gas chromatography-mass spectrometry.

Ina Kristiana1, Cynthia Joll, Anna Heitz.   

Abstract

Halonitriles are a class of nitrogen-containing disinfection by-products (DBPs) that have been reported to be more toxic and carcinogenic than the regulated DBPs. While haloacetonitriles (HANs) are often measured in drinking waters, there is little information on the formation, characteristics, and occurrence of other, higher molecular weight halonitriles. Halopropionitriles and halobutyronitriles have been predicted to be highly toxic and carcinogenic, and may have sufficient potency and selectivity to account for epidemiological associations of chlorinated and chloraminated water with adverse health effects. This paper reports on the development, optimisation, and validation of a simple, robust, and sensitive analytical method for the determination of halonitriles in waters, as well as the application of the method to study the formation and characteristics of halonitriles. This is the first reported method development for analysis halopropionitriles and halobutyronitriles, and the first study on their formation and occurrence as DBPs in drinking waters. The new method uses headspace solid-phase microextraction to extract the halonitriles from water, which are then analysed using gas chromatography-mass spectrometry (HS SPME/GC-S). The method demonstrated good sensitivity (detection limits: 0.9-80 ng L⁻¹) and good precision (repeatability: 3.8-12%), and is linear over three orders of magnitude. Matrix effects from raw drinking water containing organic carbon (4.1 mg L⁻¹) were shown to be negligible in the analysis of halonitriles. The optimised method was used to study the stability and persistence of halonitriles in aqueous samples, and the formation and occurrence of halonitriles in waters. Results from laboratory-scale disinfection experiments showed that haloacetonitriles were formed in chlorinated and chloraminated samples, but 2,2-dichloropropionitrile was only measured in chloraminated samples. Results from surveys of several drinking water distribution systems confirmed the laboratory findings.
Copyright © 2012 Elsevier B.V. All rights reserved.

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Year:  2012        PMID: 22251887     DOI: 10.1016/j.chroma.2012.01.005

Source DB:  PubMed          Journal:  J Chromatogr A        ISSN: 0021-9673            Impact factor:   4.759


  3 in total

1.  Formation of nitrogenous disinfection by-products in 10 chlorinated and chloraminated drinking water supply systems.

Authors:  Deborah Liew; Kathryn L Linge; Cynthia A Joll
Journal:  Environ Monit Assess       Date:  2016-08-14       Impact factor: 2.513

2.  An optimized analytical method for the simultaneous detection of iodoform, iodoacetic acid, and other trihalomethanes and haloacetic acids in drinking water.

Authors:  Xiaolin Liu; Xiao Wei; Weiwei Zheng; Songhui Jiang; Michael R Templeton; Gengsheng He; Weidong Qu
Journal:  PLoS One       Date:  2013-04-16       Impact factor: 3.240

3.  [Simultaneous determination of six haloacetonitriles in finished water for drinking by purge and trap-gas chromatography-triple quadrupole mass spectrometry].

Authors:  Wei Zhan; Zhiyu Han; Yong Li; Fei Liu; Yong Zhang
Journal:  Se Pu       Date:  2021-07-08
  3 in total

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