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1
Revising the EPA Dilution-Attenuation Soil Screening Model for PFAS.修订全氟和多氟烷基物质的美国环境保护局稀释-衰减土壤筛选模型。
J Hazard Mater Lett. 2023 Nov;4. doi: 10.1016/j.hazl.2023.100077. Epub 2023 Mar 20.
2
An integrated analytical modeling framework for determining site-specific soil screening levels for PFAS.用于确定特定场地全氟和多氟烷基物质(PFAS)土壤筛选水平的综合分析建模框架。
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3
PFAS concentrations in soil versus soil porewater: Mass distributions and the impact of adsorption at air-water interfaces.土壤与土壤孔隙水中的全氟烷基物质浓度:质量分布以及气-水界面吸附的影响。
Chemosphere. 2022 Sep;302:134938. doi: 10.1016/j.chemosphere.2022.134938. Epub 2022 May 11.
4
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J Contam Hydrol. 2022 Jun;248:104001. doi: 10.1016/j.jconhyd.2022.104001. Epub 2022 Mar 23.
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Air-water interfacial areas relevant for transport of per and poly-fluoroalkyl substances.与全氟和多氟烷基物质传输相关的气-水界面面积。
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Sci Total Environ. 2022 Oct 1;841:156602. doi: 10.1016/j.scitotenv.2022.156602. Epub 2022 Jun 9.
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Assessing the potential contributions of additional retention processes to PFAS retardation in the subsurface.评估额外的滞留过程对地下全氟和多氟烷基物质(PFAS)阻滞的潜在贡献。
Sci Total Environ. 2018 Feb 1;613-614:176-185. doi: 10.1016/j.scitotenv.2017.09.065. Epub 2017 Sep 12.

引用本文的文献

1
Using Suction Lysimeters for Determining the Potential of Per- and Polyfluoroalkyl Substances to Leach from Soil to Groundwater: A Review.利用吸力蒸渗仪测定全氟和多氟烷基物质从土壤淋溶到地下水的潜力:综述
Environ Sci Technol. 2025 Mar 11;59(9):4215-4229. doi: 10.1021/acs.est.4c10246. Epub 2025 Feb 27.

本文引用的文献

1
Is PFAS from land applied municipal biosolids a significant source of human exposure via groundwater?土地应用的城市生物固体中的全氟烷基物质(PFAS)是否是通过地下水导致人体暴露的重要来源?
Sci Total Environ. 2023 Mar 15;864:161154. doi: 10.1016/j.scitotenv.2022.161154. Epub 2022 Dec 23.
2
Model-based identification of vadose zone controls on PFAS mobility under semi-arid climate conditions.基于模型的半干旱气候条件下包气带控制对全氟辛烷磺酸迁移性的识别。
Water Res. 2022 Oct 15;225:119096. doi: 10.1016/j.watres.2022.119096. Epub 2022 Sep 10.
3
PFAS concentrations in soil versus soil porewater: Mass distributions and the impact of adsorption at air-water interfaces.土壤与土壤孔隙水中的全氟烷基物质浓度:质量分布以及气-水界面吸附的影响。
Chemosphere. 2022 Sep;302:134938. doi: 10.1016/j.chemosphere.2022.134938. Epub 2022 May 11.
4
A field study to assess the role of air-water interfacial sorption on PFAS leaching in an AFFF source area.一项野外研究评估了在 AFFF 源区 PFAS 浸出过程中空气-水界面吸附的作用。
J Contam Hydrol. 2022 Jun;248:104001. doi: 10.1016/j.jconhyd.2022.104001. Epub 2022 Mar 23.
5
Air-water interfacial adsorption of C4-C10 perfluorocarboxylic acids during transport in unsaturated porous media.在非饱和多孔介质中传输过程中 C4-C10 全氟羧酸在气-水界面的吸附。
Sci Total Environ. 2022 Jul 20;831:154905. doi: 10.1016/j.scitotenv.2022.154905. Epub 2022 Mar 30.
6
Air-water interfacial areas relevant for transport of per and poly-fluoroalkyl substances.与全氟和多氟烷基物质传输相关的气-水界面面积。
Water Res. 2021 Dec 1;207:117785. doi: 10.1016/j.watres.2021.117785. Epub 2021 Oct 21.
7
The impact of multiple-component PFAS solutions on fluid-fluid interfacial adsorption and transport of PFOS in unsaturated porous media.多组分全氟化合物溶液对全氟辛烷磺酸在非饱和多孔介质中液-液界面吸附和传输的影响。
Sci Total Environ. 2022 Feb 1;806(Pt 2):150595. doi: 10.1016/j.scitotenv.2021.150595. Epub 2021 Sep 28.
8
Modelling the sorption behaviour of perfluoroalkyl carboxylates and perfluoroalkane sulfonates in soils.模拟土壤中全氟羧酸和全氟烷磺酸的吸附行为。
Sci Total Environ. 2021 Dec 20;801:149343. doi: 10.1016/j.scitotenv.2021.149343. Epub 2021 Jul 30.
9
Ideal versus Nonideal Transport of PFAS in Unsaturated Porous Media.PFAS 在非饱和多孔介质中的理想与非理想输运。
Water Res. 2021 Sep 1;202:117405. doi: 10.1016/j.watres.2021.117405. Epub 2021 Jul 6.
10
The influence of molecular structure on PFAS adsorption at air-water interfaces in electrolyte solutions.分子结构对电解质溶液中空气-水界面上全氟和多氟烷基物质吸附的影响。
Chemosphere. 2021 Oct;281:130829. doi: 10.1016/j.chemosphere.2021.130829. Epub 2021 May 10.

修订全氟和多氟烷基物质的美国环境保护局稀释-衰减土壤筛选模型。

Revising the EPA Dilution-Attenuation Soil Screening Model for PFAS.

作者信息

Brusseau Mark L, Guo Bo

机构信息

Environmental Science Department, The University of Arizona, Tucson, AZ 85721.

Hydrology and Atmospheric Sciences Department, The University of Arizona, Tucson, AZ 85721.

出版信息

J Hazard Mater Lett. 2023 Nov;4. doi: 10.1016/j.hazl.2023.100077. Epub 2023 Mar 20.

DOI:10.1016/j.hazl.2023.100077
PMID:37990738
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10662647/
Abstract

Per and polyfluoroalkyl substances (PFAS) have been shown to be ubiquitous in the environment, and one issue of critical concern is the leaching of PFAS from soil to groundwater. The risk posed by contaminants present in soil is often assessed in terms of the anticipated impact to groundwater through the determination of soil screening levels (SSLs). The U.S. Environmental Protection Agency (EPA) established a soil screening model for determining SSLs. However, the model does not consider the unique retention properties of PFAS and, consequently, the SSLs established with the model may not represent the actual levels that are protective of groundwater quality. The objective of this work is to revise the standard EPA SSL model to reflect the unique properties and associated retention behavior of PFAS. Specifically, the distribution parameter used to convert soil porewater concentrations to soil concentrations is revised to account for adsorption at the air-water interface. Example calculations conducted for PFOS and PFOA illustrate the contrasting SSLs obtained with the revised and standard models. A comparison of distribution parameters calculated for a series of PFAS of different chain length shows that the significance of air-water interfacial adsorption can vary greatly as a function of the specific PFAS. Therefore, the difference between SSLs calculated with the revised versus standard models will vary as a function of the specific PFAS, with greater differences typically observed for longer-chain PFAS. It is anticipated that this revised model will be useful for developing improved SSLs that can be used to enhance site investigations and management for PFAS-impacted sites.

摘要

全氟和多氟烷基物质(PFAS)已被证明在环境中无处不在,一个备受关注的关键问题是PFAS从土壤中淋滤到地下水中。土壤中存在的污染物所带来的风险通常通过确定土壤筛选水平(SSLs)来评估对地下水的预期影响。美国环境保护局(EPA)建立了一个用于确定SSLs的土壤筛选模型。然而,该模型没有考虑PFAS独特的保留特性,因此,用该模型建立的SSLs可能无法代表保护地下水质量的实际水平。这项工作的目的是修订标准的EPA SSL模型,以反映PFAS的独特特性和相关的保留行为。具体来说,用于将土壤孔隙水浓度转换为土壤浓度的分布参数被修订,以考虑气 - 水界面的吸附作用。对全氟辛烷磺酸(PFOS)和全氟辛酸(PFOA)进行的示例计算说明了使用修订模型和标准模型获得的不同SSLs。对一系列不同链长的PFAS计算得到的分布参数进行比较表明,气 - 水界面吸附的重要性会因特定的PFAS而有很大差异。因此,用修订模型和标准模型计算出的SSLs之间的差异将因特定的PFAS而有所不同,通常对于长链PFAS观察到的差异更大。预计这个修订后的模型将有助于开发改进的SSLs,可用于加强对受PFAS影响场地的现场调查和管理。