饮用水和沉积物样品中37种PFAS同时分析方法的建立

Mingyeong Kim, Macha Fulgence Jacob, Kimberly Etombi Muambo, Wonjin Sim, Jeon-Hui Oh
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摘要

全氟烷基和多氟烷基物质(PFAS)是一种具有多种物理化学特性的合成化学品,因此很难同时分析多种PFAS。本研究基于韩国持久性有机污染物(POPs)标准方法,采用液相色谱-串联质谱法,建立了饮用水和沉积物样品中37种单氟烷基和多氟烷基物质(PFAS)的同时分析方法,包括PFAS替代化合物Gen-X、ADONA、Major F53B、Minor F53B以及前体FOSA、FOSAA、MeFOSAA、EtFOSAA、n:2 FTUA、n:3 FTCA和n:2 FTS。水样采用蜡管固相萃取法提取,沉淀物采用超声萃取法提取。准确度和精密度分别为50.7 ~ 118%和0.01 ~ 8.5%,方法检出限为0.12 ~ 1.36 ng/L。以持久性有机污染物的韩国标准分析方法为基础,对沉积物样品的PFAS分析方法进行了改进。37个目标PFAS的准确度和精密度分别为63% ~ 129%和0.6% ~ 11.7%,方法在沉积物中的检出限为0.03 ~ 1.94 ng/g。采用现行韩国标准的持久性有机污染物分析方法对水样进行了分析,结果令人满意。同时,对于沉积物样品,由于这两种化合物的结果不佳,因此对方法进行了修改。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of Simultaneous Analytical Methods of 37 PFAS in Drinking Water and Sediment Samples
Per-and polyfluoroalkyl substances (PFAS) are synthetic chemicals that exhibit various physicochemical characteristics, making it difficult to analyze many PFAS simultaneously. In this study, the simultaneous analytical methods of 37 per- and polyfluoroalkyl substances (PFAS), including the PFAS alternative compounds Gen-X, ADONA, Major F53B, Minor F53B, and precursors FOSA, FOSAA, MeFOSAA, EtFOSAA, n:2 FTUA, n:3 FTCA, and n:2 FTS in drinking water and sediment samples were developed using liquid chromatography-tandem mass spectrometry based on the Korean persistent organic pollutants (POPs) standard method. The water samples were extracted using a WAX cartridge by solid-phase extraction, while the sediment samples were extracted by ultrasonic extraction. The accuracy and precision satisfied the values of 50.7–118% and 0.01–8.5%, respectively, with a method detection limit of 0.12–1.36 ng/L. The PFAS analytical method for sediment samples was modified based on the Korean standard analytical method for persistent organic pollutants. The accuracy and precision of the 37 target PFAS ranged from 63% to 129% and 0.6% to 11.7%, respectively, with method detection limits of 0.03–1.94 ng/g in sediment. Satisfactory results were obtained for water samples using the current Korean standard analytical method for POPs. Meanwhile, for sediment samples, owing to the poor results obtained for the two compounds, the method was modified.
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