首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Determination of secondary and tertiary amines as N-nitrosamine precursors in drinking water system using ultra-fast liquid chromatography-tandem mass spectrometry
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Determination of secondary and tertiary amines as N-nitrosamine precursors in drinking water system using ultra-fast liquid chromatography-tandem mass spectrometry

机译:超快速液相色谱-串联质谱法测定饮用水系统中作为N-亚硝胺前体的仲胺和叔胺

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N-Nitrosamines are potent mutagenic and carcinogenic emerging water disinfection by-products (DBPs). The most effective strategy to control the formation of these DBPs is minimizing their precursors from source water. Secondary and tertiary amines are dominating precursors of N-nitrosamines formation during drinking water disinfection process. Therefore, the screening and removal of these amines in source water are very essential for preventing the formation of N-nitrosamines. A rapid, simple, and sensitive ultrafast liquid chromatography-tandem mass spectrometry (UFLC-MS/MS) method has been developed in this study to determine seven amines, including dimethylamine, ethylmethylamine, diethylamine, dipropylamine, trimethylamine, 3-(dimethylaminomethyl)indole, and 4-dimethylaminoantipyrine, as major precursors of N-nitrosamines in drinking water system. No sample preparation process is needed except a simple filtration. Separation and detection can be achieved in 11 min per sample. The method detection limits of selected amines are ranging from 0.02 mu g/L to 1 mu g/L except EMA (5 mu g/L), and good calibration linearity was achieved. The developed method was applied to determine the selected precursors in source water and drinking water samples collected from Midwest area of the United States. In most of water samples, the concentrations of selected precursors of N-nitrosamines were below their method detection limits. Dimethylamine was detected in some of water samples at the concentration up to 25.4 mu g/L (C) 2014 Elsevier B.V. All rights reserved.
机译:N-亚硝胺是潜在的致突变性和致癌性新兴水消毒副产物(DBP)。控制这些DBP形成的最有效策略是将源水中的前驱物减至最少。在饮用水消毒过程中,仲胺和叔胺是N-亚硝胺形成的主要前体。因此,在源水中筛选和除去这些胺对于防止N-亚硝胺的形成非常重要。本研究开发了一种快速,简单且灵敏的超快液相色谱-串联质谱(UFLC-MS / MS)方法,用于测定七种胺,包括二甲胺,乙基甲胺,二乙胺,二丙胺,三甲胺,3-(二甲氨基甲基)吲哚和4-二甲基氨基安替比林,它们是饮用水系统中N-亚硝胺的主要前体。除了简单的过滤,不需要样品制备过程。每个样品可以在11分钟内完成分离和检测。除EMA(5μg / L)外,所选胺类的方法检测限为0.02μg / L至1μg / L,并实现了良好的校准线性。所开发的方法用于确定从美国中西部地区收集的源水和饮用水样品中的选定前体。在大多数水样品中,选定的N-亚硝胺前体的浓度低于其方法检测极限。 2014年Elsevier B.V.检测到一些水样中的二甲胺浓度高达25.4μg / L(C)。保留所有权利。

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