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实验室规模和中试规模下,用稳定和固化(S/S)修复法处理受全氟和多氟烷基物质(PFASs)污染的土壤。

Laboratory-scale and pilot-scale stabilization and solidification (S/S) remediation of soil contaminated with per- and polyfluoroalkyl substances (PFASs).

机构信息

Department of Aquatic Science and Assessment, Swedish University of Agricultural Sciences, Uppsala, 750 07, Sweden.

Catalan Institute for Water Research (ICRA), Carrer Emili Grahit 101, 17003, Girona, Spain.

出版信息

J Hazard Mater. 2021 Jan 15;402:123453. doi: 10.1016/j.jhazmat.2020.123453. Epub 2020 Jul 12.

Abstract

Remediation of soil contaminated with per- and polyfluoroalkyl substances (PFAS) is critical due to the high persistence and mobility of these compounds. In this study, stabilization and solidification (S/S) treatment was evaluated at pilot-scale using 6 tons of soil contaminated with PFAS-containing aqueous film-forming foam. At pilot-scale, long-term PFAS removal over 6 years of precipitation (simulated using irrigation) in leachate from non-treated contaminated reference soil and S/S-treated soil with 15 % binder and 0.2 % GAC was compared. PFAS removal rate from leachate, corresponding to reduction in leaching potential after 6 years, was >97 % for four dominant PFASs (perfluorohexanoic acid (PFHxA), perfluorooctanoic acid (PFOA), perfluorohexanesulfonic acid (PFHxS) and perfluorooctanesulfonic acid (PFOS)), but low (3%) for short-chain perfluoropentanoic acid (PFPeA). During the pilot-scale experiment, PFAS sorption strength (i.e., soil-water partitioning coefficient (K)) increased 2- to 40-fold for both reference and S/S-treated soil, to much higher levels than in laboratory-scale tests. However, PFAS behavior in pilot-scale and laboratory-scale tests was generally well-correlated (p < 0.001), which will help in future S/S recipe optimization. In addition, seven PFASs were tentatively identified using an automated suspect screening approach. Among these, perfluorohexanesulfonamide and 3:2 fluorotelomer alcohol were tentatively identified and the latter had low removal rates from leachate (<12 %) in S/S treatment.

摘要

由于这些化合物具有高持久性和高迁移性,因此修复受全氟和多氟烷基物质 (PFAS) 污染的土壤至关重要。在本研究中,使用 6 吨受含全氟烷基物质的水性成膜泡沫污染的土壤,在中试规模下评估了稳定化/固化 (S/S) 处理。在中试规模下,通过用灌溉模拟的降水(长达 6 年),比较了未经处理的污染对照土壤和用 15%粘结剂和 0.2%GAC 处理的 S/S 土壤的沥出液中 PFAS 的长期去除情况。从沥出液中去除 PFAS 的速度(对应于 6 年后浸出潜力的降低),对于四种主要的 PFAS(全氟己酸 (PFHxA)、全氟辛酸 (PFOA)、全氟己烷磺酸 (PFHxS) 和全氟辛烷磺酸 (PFOS)),超过 97%,但对于短链全氟戊酸 (PFPeA) 则较低(3%)。在中试规模实验过程中,对于对照和 S/S 处理的土壤,PFAS 的吸附强度(即土壤-水分配系数 (K)) 增加了 2-40 倍,达到比实验室规模测试高得多的水平。然而,中试规模和实验室规模测试中 PFAS 的行为通常具有很好的相关性(p < 0.001),这将有助于未来的 S/S 配方优化。此外,使用自动可疑筛选方法初步鉴定了七种 PFAS。在这些中,初步鉴定了全氟己烷磺酰胺和 3:2 氟代醇,并且后者在 S/S 处理中从沥出液中的去除率较低(<12%)。

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