首页> 外文期刊>International journal of environmental analytical chemistry >In situ acetylation dispersive liquid-liquid microextraction followed by gas chromatography-mass spectrometry for the simultaneous determination of musks, triclosan and methyl-triclosan in wastewaters
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In situ acetylation dispersive liquid-liquid microextraction followed by gas chromatography-mass spectrometry for the simultaneous determination of musks, triclosan and methyl-triclosan in wastewaters

机译:原位乙酰化分散液-液微萃取-气相色谱-质谱法同时测定废水中的麝香,三氯生和甲基三氯生

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摘要

A rapid and environmental-friendly analytical method for the simultaneous analysis of different personal care products (PCPs) namely synthetic musks (nitro-, polycyclic and macrocyclic musks) and the disinfectant triclosan (TCS) and its transformation product methyl-TCS in wastewater samples has been developed. The method combines dispersive liquid-liquid microextraction with in situ aqueous derivatisation using acetic anhydride (Ac2O) prior to gas chromatography-mass spectrometry analysis. Several parameters affecting both extraction and derivatisation efficiency (e.g. type and volume of extractor and dispersive solvents, volume of derivatising reagent, etc.) were optimised to achieve reliable conditions. Validation of the method for all compounds under study showed good linearity with coefficient of correlation 0.9947. Limits of quantification (LOQs) ranged between 2 and 72 ng/L for musks and 28 and 31 ng/L for TCS and methyl-TCS, respectively. Accuracy, expressed as the average recoveries, ranged between 76% and 87%, and precision, expressed in terms of intraday repeatability (%RSD), was better than 13% for all analytes. The application of the method to the analysis of 24 wastewater samples enabled the detection of all the target PCPs at concentration levels up to 2.7 mu g/L, being galaxolide (HHCB) and tonalide (AHTN) the more prevalent, present in 88% and 46% of the samples, respectively.
机译:快速,环保的分析方法可以同时分析废水样品中的各种个人护理产品(PCP),即合成麝香(硝基,多环和大环麝香)和消毒剂三氯生(TCS)及其转化产物甲基-TCS已开发。在气相色谱-质谱分析之前,该方法将分散液-液微萃取与使用乙酸酐(Ac2O)的原位水溶液衍生化相结合。优化了影响萃取和衍生化效率的几个参数(例如萃取器和分散溶剂的类型和体积,衍生化试剂的体积等)以实现可靠的条件。对所研究的所有化合物进行的方法验证均显示出良好的线性,相关系数> 0.9947。麝香的定量限(LOQ)分别为2到72 ng / L,TCS和甲基TCS的定量限分别为28和31 ng / L。对于所有分析物,以平均回收率表示的准确度在76%至87%之间,以日内重复性(%RSD)表示的精度优于13%。该方法应用于24个废水样品的分析,能够检测浓度高达2.7μg / L的所有目标五氯苯酚,其中galaxolide(HHCB)和Tonalide(AHTN)更为普遍,占88%和分别有46%的样本。

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