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Trace Analysis of N-Nitrosamines in Water Using Solid-Phase Microextraction Coupled with Gas Chromatograph–Tandem Mass Spectrometry

机译:固相微萃取-气相色谱-串联质谱联用法分析水中的N-亚硝胺

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摘要

A method that utilizes solid-phase microextraction (SPME) coupled with gas chromatography (GC) and chemical ionization tandem mass spectrometry (MS/MS) was developed for analyzing a group of emerging pollutants, N-nitrosamines, in water. The developed analytical method requires a water sample of less than 5 ml and only 1.5 h for complete analysis. The method detection limits for N-nitrosodimethylamine (NDMA), N-nitrosodiethylamine, and N-nitrosodi-n-propylamine were in the range of 3.2 to 3.5 ng/l; for N-nitrosomorpholine, it was 15.2 ng/l. The method was successfully employed to measure the N-nitrosamine concentration at trace levels of nanogram per liter in four water treatment plants (WTPs) and one water distribution system. In the WTPs, only NDMA was detected in the treatment processes. Within the treatment train, NDMA was observed after chlorination. The level of NDMA significantly declined after slow sand filtration due presumably to microbial degradation. The NDMA concentration collected from consumer tap water was about 40% higher on average than that in the finished water. The excellent performance of the SPME/GC/MS/MS method in various water matrices as well as the shorter analysis time and smaller sample volume compared to currently used extraction techniques makes it an alternative means for the analysis of N-nitrosamine in drinking water, wastewater, and laboratory research with small reactors.
机译:开发了一种利用固相微萃取(SPME)结合气相色谱(GC)和化学电离串联质谱(MS / MS)的方法来分析水中的一组新兴污染物N-亚硝胺。开发的分析方法需要少于5 ml的水样,仅需1.5 h即可进行完整分析。 N-亚硝基二甲胺(NDMA),N-亚硝基二乙胺和N-亚硝基二正丙胺的方法检出限为3.2至3.5 ng / l; N-亚硝基吗啉为15.2 ng / l。该方法已成功地用于在四个水处理厂(WTP)和一个水分配系统中以痕量纳克每升的水平测量N-亚硝胺的浓度。在WTP中,在处理过程中仅检测到NDMA。在处理过程中,氯化后观察到NDMA。缓慢的砂滤后,NDMA的水平显着下降,可能是由于微生物降解所致。从消费者自来水中收集的NDMA浓度平均比成品水高40%。与目前使用的萃取技术相比,SPME / GC / MS / MS方法在各种水基质中均具有出色的性能,并且分析时间短且样品量小,这使其成为分析饮用水中N-亚硝胺的另一种方法,废水,以及小型反应器的实验室研究。

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