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Determination of Volatile Disinfection Byproducts in Water by Gas Chromatography-Triple Quadrupole Mass Spectrometry

机译:气相色谱-三重四极杆质谱法测定水中的挥发性消毒副产物

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摘要

Chlorination disinfection byproducts have drawn significant attention in water quality research during the last decades, due to their adverse effects on public health. A method is reported for the determination of trihalomethanes, haloacetonitriles, haloketones, and chloropicrin based on liquid-liquid extraction and gas chromatography-tandem mass spectrometry. The optimum electron ionization energy was determined and precursor ions and product ions for thirteen volatile disinfection byproducts were identified. The method provides rapid chromatographic analysis (10 minutes) and good separation. The linear dynamic range extended from 0.05 to 100 mu gL(-1) (r(2)=0.9983-0.9997, n=10) and the limits of detection (LODs) were between 0.003 and 0.014 mu gL ( -1 ). The intra-day (n=5) and inter-day (n=6) relative standard deviations were in the ranges of 2.81-8.22% and 3.48-10.85%, respectively. The method was validated by measurement of the recoveries of fortified surface, ground, and wastewater to be 74.7-115.4%, 86.1-120.6%, and 81.6-126.1%, respectively.
机译:氯化消毒副产物由于其对公众健康的不利影响而在过去几十年中引起了水质研究的极大关注。报道了一种基于液-液萃取和气相色谱-串联质谱法测定三卤甲烷,卤代乙腈,卤代酮和氯吡啶的方法。确定了最佳电子电离能,并确定了13种挥发性消毒副产物的前体离子和产物离子。该方法提供快速色谱分析(10分钟)和良好的分离效果。线性动态范围从0.05扩展到100μgL(-1)(r(2)= 0.9983-0.9997,n = 10),检出限(LOD)在0.003至0.014μgL(-1)之间。日内(n = 5)和日间(n = 6)相对标准偏差分别在2.81-8.22%和3.48-10.85%的范围内。通过测量强化表面,地面和废水的回收率分别验证该方法为74.7-115.4%,86.1-120.6%和81.6-126.1%。

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