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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Dispersive liquid-liquid microextraction applied to the simultaneous derivatization and concentration of triclosan and methyltriclosan in water samples
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Dispersive liquid-liquid microextraction applied to the simultaneous derivatization and concentration of triclosan and methyltriclosan in water samples

机译:分散液-液微萃取用于水样中三氯生和甲基三氯生的同时衍生和浓缩

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摘要

A fast and novel sample preparation procedure for the determination of triclosan (TCS) and methyltriclosan (MTCS) in water samples is presented. Dispersive liquid-liquid microextraction, using a ternary mixture consisting of a disperser, an extractant and N-methyl-N-(tert-butyldimethylsilyl) trifluoroacetamide (MTBSTFA) as derivatization reagent, was used for the simultaneous derivatization, case of TCS, and concentration of both species in different water samples. Analytes were determined by gas chromatography with tandem mass spectrometry (GC-MS/MS). Influence of different factors on the performance of the sample preparation process is thoroughly discussed. Under final working conditions, a mixture of 1 mL, of methanol, 40 mu L of 1,1,1-trichloroethane and the same volume of MTBSTFA was added to 10 mL of water in a conical bottom glass tube. After centrifugation, the settled phase was injected directly in the chromatographic system. TCS was quantitatively extracted and converted into the corresponding tert-butyldimethylsilyl derivative, whereas for MTCS an extraction yield around 90% was attained. Limits of quantification between 2 and 5 ng L-1 and reproducibility values below 10% were achieved: moreover, the performance of the extraction process was scarcely affected by the type of water sample. Globally, these values are comparable, or even better, to those reported for other approaches applied to the determination of same compounds, with the advantage of a shorter sample preparation step. Analysis of surface and wastewater samples confirmed the ubiquitous presence of TCS in the aquatic environment at levels from 20 to 700 ng L-1. (C) 2008 Elsevier B.V. All rights reserved.
机译:提出了一种快速,新颖的样品前处理方法,用于测定水样中的三氯生(TCS)和甲基三氯生(MTCS)。使用由分散剂,萃取剂和N-甲基-N-(叔丁基二甲基甲硅烷基)三氟乙酰胺(MTBSTFA)组成的三元混合物作为衍生试剂的分散液-液微萃取用于同时衍生,TCS情况和浓缩两种样品在不同水样中的含量通过气相色谱-串联质谱法(GC-MS / MS)测定分析物。彻底讨论了不同因素对样品制备过程性能的影响。在最终工作条件下,将1 mL甲醇,40μL 1,1,1-三氯乙烷和相同体积的MTBSTFA的混合物添加到锥形底部玻璃管中的10 mL水中。离心后,将沉淀的相直接注入色谱系统中。定量提取TCS并将其转化为相应的叔丁基二甲基甲硅烷基衍生物,而对于MTCS而言,提取率约为90%。达到了2到5 ng L-1的定量极限,并且再现性值低于10%:此外,萃取过程的性能几乎不受水样类型的影响。在全球范围内,这些值与用于测定相同化合物的其他方法所报告的值相当,甚至更好,其优点是样品制备步骤更短。对地表和废水样品的分析证实,水生环境中TCS的存在量为20至700 ng L-1。 (C)2008 Elsevier B.V.保留所有权利。

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