Selective Quantification of Charged and Neutral Polyfluoroalkyl Substances Using the Total Oxidizable Precursor (TOP) Assay

IF 11.3 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL
Edmund H. Antell, Shan Yi, Christopher I. Olivares, Shreya Chaudhuri, Bridger J. Ruyle, Lisa Alvarez-Cohen and David L. Sedlak*, 
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引用次数: 0

Abstract

Perfluoroalkyl acid (PFAA) precursors are a diverse subclass of per- and polyfluoroalkyl substances (PFASs) that can be transformed into PFAAs of public health concern. Unlike strongly acidic PFAAs, precursors can be anionic, cationic, neutral, or zwitterionic. Precursor charge affects the environmental fate, but existing quantification techniques struggle to ascertain the abundance of compounds within each charge group. To fill this gap, we developed and validated a solid-phase extraction procedure that separates precursors by charge and quantifies the sum of the precursors in each fraction with the total oxidizable precursor (TOP) assay. Method performance was demonstrated by spiking known concentrations of ten precursors into aqueous film-forming foam (AFFF)-impacted groundwater, municipal wastewater, and soil samples. Precursor fractionation and recovery were greater in groundwater and soil samples than in wastewater. Use of the method provided results that were consistent with expectations based on precursor transport properties. In surficial soils near an AFFF source zone, anionic precursors with five or fewer perfluorinated carbons accounted for about 95% of PFASs, but less than half of PFASs in the underlying groundwater. In municipal wastewater influent, the sum of precursors exceeded the sum of PFAAs and was approximately equally distributed among all charge fractions.

A method to quantify perfluoroalkyl acid precursors by charge state was developed and applied to environmental samples to assess the effect of precursor charge on contaminant fate.

用总可氧化前体(TOP)测定法选择性定量带电和中性多氟烷基物质
全氟烷基酸(PFAA)前体是单氟烷基和多氟烷基物质(PFASs)的一个不同亚类,可转化为引起公共卫生关注的全氟烷基物质。与强酸性PFAAs不同,前体可以是阴离子、阳离子、中性或两性离子。前体电荷影响环境命运,但现有的定量技术难以确定每个电荷组内化合物的丰度。为了填补这一空白,我们开发并验证了一种固相萃取方法,该方法通过电荷分离前驱体,并用总氧化前驱体(TOP)测定法定量每个馏分中前驱体的总和。通过将已知浓度的十种前体加入受AFFF影响的水成膜泡沫(AFFF)地下水、城市废水和土壤样品中,证明了该方法的性能。前驱体在地下水和土壤样品中的分馏和回收率高于废水。使用该方法提供的结果与基于前驱体输运性质的预期一致。在AFFF源区附近的表层土壤中,含有5个或更少的全氟碳的阴离子前体约占全氟磺酸的95%,但在地下水中不到一半。在城市污水中,前驱体的总和大于PFAAs的总和,并且在各电荷段中近似均匀分布。建立了一种以电荷状态定量全氟烷基酸前体的方法,并将其应用于环境样品中,以评估前体电荷对污染物命运的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
环境科学与技术
环境科学与技术 环境科学-工程:环境
CiteScore
17.50
自引率
9.60%
发文量
12359
审稿时长
2.8 months
期刊介绍: Environmental Science & Technology (ES&T) is a co-sponsored academic and technical magazine by the Hubei Provincial Environmental Protection Bureau and the Hubei Provincial Academy of Environmental Sciences. Environmental Science & Technology (ES&T) holds the status of Chinese core journals, scientific papers source journals of China, Chinese Science Citation Database source journals, and Chinese Academic Journal Comprehensive Evaluation Database source journals. This publication focuses on the academic field of environmental protection, featuring articles related to environmental protection and technical advancements.
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