School of Water Resources & Environment, China University of Geosciences (Beijing), Beijing, 100083, PR China; Environmental Science Department, University of Arizona, Tucson, AZ, 85721, United States.
Department of Plant & Environmental Sciences, New Mexico State University, MSC 3167, Las Cruces, NM, 88003-8001, United States.
Chemosphere. 2022 Jan;286(Pt 3):131834. doi: 10.1016/j.chemosphere.2021.131834. Epub 2021 Aug 7.
PFAS and Cr are present at some sites as co-contaminants. The objective of this research was to investigate the co-transport behavior of per- and polyfluoroalkyl substances (PFAS) and hexavalent chromium (Cr(VI)) in porous media. Miscible-displacement experiments were conducted using two soils and an aquifer sediment with different geochemical properties. Perfluorooctane sulfonic acid (PFOS) and perfluorooctanoic acid (PFOA) were employed as model PFAS. The retardation of PFOS was decreased in the presence of Cr(VI). Conversely, the transport and retardation of PFOA was not affected by the presence of Cr(VI). The reduction of PFOS retardation caused by Cr(VI) is likely due to sorption competition for both organic-carbon and inorganic (metal-oxides and clay minerals) domains. The relative contributions of the three soil constituents to PFOS sorption and the potential for competition between PFOS and Cr(VI) is a function of the geochemical composition of the porous media (i.e., organic carbon, metal-oxides and clay minerals). The PFAS had minimal impact on the retention and transport of Cr(VI). To our knowledge, the results presented herein represent the first reported data for PFOS and Cr(VI) co-transport in porous media. The results of this study indicate that the presence of Cr(VI) has the potential to increase the migration potential of PFOS in soil and groundwater, which should be considered when characterizing electroplating facilities, leather tanning facilities, and other co-contaminated sites.
PFAS 和 Cr 作为共污染物存在于一些地点。本研究的目的是研究全氟和多氟烷基物质 (PFAS) 和六价铬 (Cr(VI)) 在多孔介质中的共迁移行为。使用具有不同地球化学性质的两种土壤和含水层沉积物进行了混相驱替实验。全氟辛烷磺酸 (PFOS) 和全氟辛酸 (PFOA) 被用作 PFAS 的模型化合物。PFOS 的滞留率在 Cr(VI) 的存在下降低。相反,PFOA 的迁移和滞留率不受 Cr(VI) 的影响。Cr(VI) 降低 PFOS 滞留率的原因可能是有机碳和无机(金属氧化物和粘土矿物)域的吸附竞争。三种土壤成分对 PFOS 吸附的相对贡献以及 PFOS 和 Cr(VI) 之间竞争的可能性是多孔介质地球化学组成的函数(即有机碳、金属氧化物和粘土矿物)。PFAS 对 Cr(VI) 的保留和迁移影响很小。据我们所知,本文所呈现的结果代表了 PFOS 和 Cr(VI) 在多孔介质中共同迁移的首批报告数据。本研究结果表明,Cr(VI) 的存在有可能增加 PFOS 在土壤和地下水中的迁移潜力,在对电镀设施、制革厂和其他共存污染地点进行特征描述时应予以考虑。