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优先保留和传输全氟辛烷磺酸在白云石含水层。

Preferential Retention and Transport of Perfluorooctanesulfonic Acid in a Dolomite Aquifer.

机构信息

USGS New York Water Science Center, Troy, NY, USA.

Department of Geosciences, The Pennsylvania State University, University Park, PA.

出版信息

Ground Water. 2023 May-Jun;61(3):318-329. doi: 10.1111/gwat.13255. Epub 2022 Oct 7.

DOI:10.1111/gwat.13255
PMID:36103019
Abstract

Per- and polyfluoroalkyl substances (PFAS) can represent a significant human health risk if present in aquifers used as a drinking water source. Accurate assessment of PFAS exposure risks requires an improved understanding of field-scale PFAS transport in groundwater. Activities at a former firefighter training site in University Park, Pennsylvania introduced perfluorooctanesulfonic acid (PFOS) to the underlying dolomite aquifer. Groundwater sampling from 2015 to 2018 delineated a PFOS plume with two concentration maxima located approximately 20 and approximately 220 m downgradient of the training site, separated by a zone of lower concentrations. We use a combination of analytical and numerical models, informed by independent measurements of aquifer porosity, hydraulic conductivity, and organic carbon content, to interpret the field observations. Our analysis demonstrates that preferential retention and transport resulting from simple heterogeneity in bedrock sorption, as caused by organic carbon (OC) content variability, provides a plausible explanation for plume separation. Dissolved PFOS partitions strongly to organic solids (high K ), so even a small OC (<1 wt%) significantly retards PFOS transport, whereas zones with little to no OC allow for transport rates that approximate those of a conservative solute. Our work highlights an important consideration for modeling the groundwater transport of PFOS, and other compounds with high K . In aquifers with discrete layers of varying OC, models using a uniform site-average OC will underestimate transport distances, thereby misrepresenting exposure risks for downgradient communities.

摘要

全氟和多氟烷基物质 (PFAS) 如果存在于用作饮用水源的含水层中,可能会对人类健康造成重大风险。准确评估 PFAS 暴露风险需要更好地了解地下水环境中 PFAS 的迁移。宾夕法尼亚州大学公园的一个前消防员培训场地的活动将全氟辛烷磺酸 (PFOS) 引入了下方的白云石含水层。2015 年至 2018 年的地下水采样描绘了一个 PFOS 羽流,在培训场地的下游约 20 和 220 米处有两个浓度最大值,其间有一个浓度较低的区域。我们结合分析和数值模型,利用含水层孔隙率、水力传导率和有机碳含量的独立测量结果进行解释。我们的分析表明,由于有机碳 (OC) 含量变化引起的基岩吸附的简单非均质性导致的优先保留和传输,为羽流分离提供了一个合理的解释。溶解的 PFOS 强烈分配到有机固体(高 K),因此即使 OC 含量很小(<1wt%)也会显著减缓 PFOS 的迁移,而几乎没有或没有 OC 的区域允许接近保守溶质的迁移速率。我们的工作强调了在 PFOS 以及其他具有高 K 的化合物的地下水迁移建模中需要考虑的一个重要因素。在具有不同 OC 离散层的含水层中,使用统一的站点平均 OC 的模型将低估迁移距离,从而错误地表示下游社区的暴露风险。

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