用于分析总氟、可吸附氟和可萃取有机氟的燃烧离子色谱法综述。

IF 2.8 3区 工程技术 Q2 CHEMISTRY, ANALYTICAL
Charles Phillip Shelor, Cable Warren, Chimauchem V. Odinaka, Kalpana Dumre
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引用次数: 0

摘要

聚全氟烷基和全氟烷基化合物(PFAS)是一类持久性有机污染物,其高度稳定性和明显的水溶性导致了近乎全球性的污染。PFAS 是一种生物蓄积性毒素,与多种疾病有关,在人体血液中几乎都能检测到。液相色谱-串联质谱法是最常用的定量方法,不过这种方法通常只能检测出 14 000 多种已知 PFAS 中的几十种,而且只占有机氟总量的一小部分。总参数法(如总有机氟、可萃取有机氟和可吸附有机氟)已成为测定 PFAS 的替代测量方法。燃烧离子色谱法已成为测量有机氟的首选方法,在这种方法中,含有 PFAS 的吸附剂或萃取物被燃烧,排放出的氢氟酸 (HF) 可用于测量存在的累积有机氟。在此,我们将对有机氟测量的类型、有机氟与样品基质的分离以及影响 PFAS 分析灵敏度、重现性和回收率的分析仪器的关键参数进行严格审查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comprehensive review of combustion ion chromatography for the analysis of total, adsorbable, and extractable organic fluorine

Poly- and perfluoroalkyl substances (PFAS) are a class of persistent organic pollutants whose high stability and appreciable water solubility have led to near-global contamination. PFAS are bioaccumulative toxins that have been linked to a myriad of disorders and have been detected nearly universally in human blood. Liquid chromatography-tandem mass spectrometry is the most frequent method used for quantitation, though this typically only measures a few dozen of the >14 000 known PFAS and has been shown to account for a small portion of the total organic fluorine present. Sum parameter methods such as total, extractable, and adsorbable organic fluorine have emerged as alternative measurements for PFAS determination. Combustion ion chromatography has become the preferred method for organofluorine measurement where the sorbent or extract containing PFAS is combusted and the emitted hydrofluoric acid (HF) is a measure of the cumulative organofluorine present. Herein we critically review the types of organofluorine measurement, their separation from the sample matrix, and key parameters of the analytical instrument that affect sensitivity, reproducibility, and recovery with regards to PFAS analysis.

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来源期刊
Journal of separation science
Journal of separation science 化学-分析化学
CiteScore
6.30
自引率
16.10%
发文量
408
审稿时长
1.8 months
期刊介绍: The Journal of Separation Science (JSS) is the most comprehensive source in separation science, since it covers all areas of chromatographic and electrophoretic separation methods in theory and practice, both in the analytical and in the preparative mode, solid phase extraction, sample preparation, and related techniques. Manuscripts on methodological or instrumental developments, including detection aspects, in particular mass spectrometry, as well as on innovative applications will also be published. Manuscripts on hyphenation, automation, and miniaturization are particularly welcome. Pre- and post-separation facets of a total analysis may be covered as well as the underlying logic of the development or application of a method.
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