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受历史悠久的全氟和多氟烷基物质(PFAS)废物场地影响的地表水和地下水的非靶向分析。

Nontargeted Analysis of Surface and Groundwaters Impacted by Historic PFAS Waste Sites.

作者信息

Whitehead Heather D, Buckley Timothy J, Sobus Jon R, Bangma Jacqueline, MacMillan Denise K, Williams Antony J, Janesch Gregory, Coombs James, Newman Erin, Dahlmeier Andri, Saravia Stefan, Rushing Rosie, DeVault Marla, McCord James P

机构信息

U.S. Environmental Protection Agency, Office of Research and Development, Research Triangle Park, North Carolina 27711, United States.

Oak Ridge Associated Universities (ORAU), Research Triangle Park, North Carolina 27711, United States.

出版信息

Environ Sci Technol. 2025 Jul 1;59(25):13000-13011. doi: 10.1021/acs.est.5c03243. Epub 2025 Jun 17.

DOI:10.1021/acs.est.5c03243
PMID:40528355
Abstract

Per- and polyfluoroalkyl substances (PFAS) make up a diverse class of anthropogenic chemicals with widespread industrial and commercial uses. Historical manufacturing and disposal of PFAS have led to their introduction to the environment, although only a fraction of existing PFAS are routinely monitored using targeted analysis methods. Here, nontargeted analysis was used to investigate the identity and fate of PFAS present in eight groundwater and nine surface water samples collected near St. Paul, MN, surrounding two sites that historically received wastes from a PFAS manufacturer in the 1940-1970s. A total of 210 PFAS, split across 33 different homologous series, were identified in surface and groundwater samples both at and downstream of the two waste sites. Identified compounds included perfluorinated, polyfluorinated, and unsaturated sulfonic and carboxylic acid species as well as a variety of sulfonamide and sulfonamido chemistries. PFAS measured downgradient included legacy perfluorinated sulfonic and carboxylic acids, as well as their polyfluorinated, unsaturated, keto, and ether-containing analogs. Two-thirds of the identified PFAS were unique to the groundwater at one site. The lack of these PFAS at downstream sites likely reflects dilution below the limit of detection during downgradient transport. The identified species reveal previously unknown and substantial ongoing contamination of the watershed due to historic PFAS manufacturing and waste disposal.

摘要

全氟和多氟烷基物质(PFAS)是一类多样的人为化学品,具有广泛的工业和商业用途。PFAS过去的生产和处置导致其进入环境,尽管目前只有一小部分现有的PFAS使用目标分析方法进行常规监测。在此,采用非目标分析方法来研究明尼苏达州圣保罗市附近采集的8个地下水和9个地表水样品中PFAS的种类和归宿,这些样品围绕着两个在20世纪40年代至70年代历史上接收过PFAS制造商废弃物的场地。在两个废弃物场地及其下游的地表水和地下水样品中,共鉴定出210种PFAS,分属于33个不同的同系物系列。鉴定出的化合物包括全氟、多氟以及不饱和磺酸和羧酸类物质,还有各种磺酰胺和磺酰胺基化合物。在下游测得的PFAS包括传统的全氟磺酸和羧酸,以及它们的多氟、不饱和、含酮和含醚类似物。在其中一个场地,三分之二鉴定出的PFAS是该地下水所特有的。下游场地缺乏这些PFAS可能反映出在下游运移过程中稀释至检测限以下。鉴定出的这些物质揭示了由于历史上PFAS的生产和废物处置,该流域存在此前未知且仍在持续的大量污染。

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