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受水成膜泡沫影响的地下水中全氟烷基酸(PFAA)前体和 PFAAs 的电化学转化。

Electrochemical Transformations of Perfluoroalkyl Acid (PFAA) Precursors and PFAAs in Groundwater Impacted with Aqueous Film Forming Foams.

机构信息

CDM Smith , 110 Fieldcrest Avenue, #8, Sixth Floor , Edison , New Jersey 08837 , United States.

Nicholas School of the Environment , Duke University , Durham , North Carolina 27708 , United States.

出版信息

Environ Sci Technol. 2018 Sep 18;52(18):10689-10697. doi: 10.1021/acs.est.8b02726. Epub 2018 Aug 31.

DOI:10.1021/acs.est.8b02726
PMID:30130962
Abstract

While oxidative technologies have been proposed for treatment of waters impacted by aqueous film forming foams (AFFFs), information is lacking regarding the transformation pathways for the chemical precursors to the perfluoroalkyl acids (PFAAs) typically present in such waters. This study examined the oxidative electrochemical treatment of poly- and perfluoroalkyl substances (PFASs) for two AFFF-impacted groundwaters. The bulk pseudo first order rate constant for PFOA removal was 0.23 L h A; for PFOS, this value ranged from 0.084 to 0.23 L h A. Results from the first groundwater studied suggested a transformation pathway where sulfonamide-based PFASs transformed to primarily perfluorinated sulfonamides and perfluorinated carboxylic acids (PFCAs), with subsequent defluorination of the PFCAs. Transient increases in the perfluorinated sulfonamides and PFCAs were observed. For the second groundwater studied, no transient increases in PFAAs were measured, despite the presence of similarly structured suspected PFAA precursors and substantial defluorination. For both waters, suspected precursors were the primary sources of the generated fluoride. Assessment of precursor compound transformation noted the formation of keto-perfluoroalkanesulfonates only in the second groundwater. These results confirm that oxidation and defluorination of suspected PFAA precursors in the second groundwater underwent transformation via a pathway different than that of the first groundwater, which was not captured by total oxidizable precursor assay.

摘要

虽然已经提出了氧化技术来处理受水成膜泡沫(AFFFs)影响的水,但对于通常存在于此类水中的全氟烷基酸(PFAAs)的化学前体的转化途径的信息却很缺乏。本研究考察了两种受 AFFF 影响的地下水的多氟和全氟烷基物质(PFASs)的氧化电化学处理。PFOA 去除的整体拟一级速率常数为 0.23 L h A;对于 PFOS,该值范围为 0.084 至 0.23 L h A。第一个地下水的研究结果表明了一种转化途径,其中基于磺酰胺的 PFASs 转化为主要的全氟磺酰胺和全氟羧酸(PFCAs),随后 PFCAs 发生脱氟。观察到短暂增加了全氟磺酰胺和 PFCAs。对于第二个地下水的研究,尽管存在类似结构的疑似 PFAA 前体和大量脱氟,但未测量到 PFAAs 的短暂增加。对于这两种水,疑似前体是生成氟化物的主要来源。对前体化合物转化的评估指出,只有在第二种地下水中才形成了酮基全氟烷基亚磺酸盐。这些结果证实,第二个地下水中疑似 PFAA 前体的氧化和脱氟通过不同于第一个地下水的途径进行了转化,而总可氧化前体测定法并未捕获到该途径。

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