首页> 美国卫生研究院文献>The Journal of Automatic Chemistry >An On-Line Solid Phase Extraction-Liquid Chromatography-Tandem Mass Spectrometry Method for the Determination of Perfluoroalkyl Acids in Drinking and Surface Waters
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An On-Line Solid Phase Extraction-Liquid Chromatography-Tandem Mass Spectrometry Method for the Determination of Perfluoroalkyl Acids in Drinking and Surface Waters

机译:在线固相萃取-液相色谱-串联质谱法测定饮用水和地表水中的全氟烷基酸

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摘要

An UHPLC-MS/MS multiresidue method based on an on-line solid phase extraction (SPE) procedure was developed for the simultaneous determination of 9 perfluorinated carboxylates (from 4 to 12 carbon atoms) and 3 perfluorinated sulphonates (from 4 to 8 carbon atoms). This work proposes using an on-line solid phase extraction before chromatographic separation and analysis to replace traditional methods of off-line SPE before direct injection to LC-MS/MS. Manual sample preparation was reduced to sample centrifugation and acidification, thus eliminating several procedural errors and significantly reducing time-consuming and costs. Ionization suppression between target perfluorinated analytes and their coeluting SIL-IS were detected for homologues with a number of carbon atoms less than 9, but the quantitation was not affected. Total matrix effect corrected by SIL-IS, inclusive of extraction efficacy, and of ionization efficiency, ranged between −34 and +39%. The percentage of recoveries, between 76 and 134%, calculated in different matrices (tap water and rivers impacted by different pollutions) was generally satisfactory. LODs and LOQs of this on-line SPE method, which also incorporate recovery losses, ranged from 0.2 to 5.0 ng/L and from 1 to 20 ng/L, respectively. Validated on-line SPE-LC/MS/MS method has been applied in a wide survey for the determination of perfluoroalkyl acids in Italian surface and ground waters.
机译:开发了一种基于在线固相萃取(SPE)程序的UHPLC-MS / MS多残留方法,用于同时测定9种全氟羧酸盐(4至12个碳原子)和3种全氟磺酸盐(4至8个碳原子) )。这项工作建议在色谱分离和分析之前使用在线固相萃取,以替代直接进样到LC-MS / MS之前的离线SPE的传统方法。手动样品制备减少到样品离心和酸化,从而消除了一些程序错误,并大大减少了时间和成本。对于碳原子数少于9的同系物,检测到目标全氟化分析物与其共洗脱SIL-IS之间的电离抑制,但定量没有受到影响。通过SIL-IS校正的总基质效应(包括萃取效率和电离效率)介于-34%至+ 39%之间。在不同基质(自来水和受到不同污染影响的河流)中计算出的回收率在76%至134%之间,总体上令人满意。这种在线SPE方法的LOD和LOQ也包括回收损失,范围分别为0.2至5.0 ng / L和1至20 ng / L。经过验证的在线SPE-LC / MS / MS方法已用于广泛的调查中,用于测定意大利地表水和地下水中的全氟烷基酸。

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