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地下水受水系灭火剂(AFFFs)影响时,全氟辛酸(PFOA)和全氟辛烷磺酸(PFOS)的电化学处理。

Electrochemical treatment of perfluorooctanoic acid (PFOA) and perfluorooctane sulfonic acid (PFOS) in groundwater impacted by aqueous film forming foams (AFFFs).

机构信息

CB&I Federal Services, LLC, 17 Princess Road, Lawrenceville, NJ 08648, USA.

CB&I Federal Services, LLC, 17 Princess Road, Lawrenceville, NJ 08648, USA.

出版信息

J Hazard Mater. 2015 Sep 15;295:170-5. doi: 10.1016/j.jhazmat.2015.04.024. Epub 2015 Apr 10.

DOI:10.1016/j.jhazmat.2015.04.024
PMID:25909497
Abstract

Laboratory experiments were performed to evaluate the use of electrochemical treatment for the decomposition of perfluorooctanoic acid (PFOA) and perfluorooctane sulfonic acid (PFOS), as well as other perfluoroalkyl acids (PFAAs), in aqueous film forming foam (AFFF)-impacted groundwater collected from a former firefighter training area and PFAA-spiked synthetic groundwater. Using a commercially-produced Ti/RuO2 anode in a divided electrochemical cell, PFOA and PFOS decomposition was evaluated as a function of current density (0-20 mA/cm(2)). Decomposition of both PFOA and PFOS increased with increasing current density, although the decomposition of PFOS did not increase as the current density was increased above 2.5 mA/cm(2). At a current density of 10 mA/cm(2), the first-order rate constants, normalized for current density and treatment volume, for electrochemical treatment of both PFOA and PFOS were 46 × 10(-5) and 70 × 10(-5) [(min(-1)) (mA/cm(2))(-1) (L)], respectively. Defluorination was confirmed for both PFOA and PFOS, with 58% and 98% recovery as fluoride, respectively (based upon the mass of PFOA and PFOS degraded). Treatment of other PFAAs present in the groundwater also was observed, with shorter chain PFAAs generally being more recalcitrant. Results highlight the potential for electrochemical treatment of PFAAs, particularly PFOA and PFOS, in AFFF-impacted groundwater.

摘要

实验室实验评估了电化学处理在分解全氟辛酸 (PFOA) 和全氟辛烷磺酸 (PFOS) 以及其他全氟烷基酸 (PFAAs) 方面的应用,这些物质存在于从前的消防员训练区采集的水成膜泡沫 (AFFF) 污染地下水中以及添加了 PFAAs 的合成地下水中。使用商业生产的 Ti/RuO2 阳极在分隔的电化学电池中,评估了电流密度 (0-20 mA/cm(2)) 对 PFOA 和 PFOS 分解的影响。随着电流密度的增加,PFOA 和 PFOS 的分解都增加了,尽管当电流密度增加到 2.5 mA/cm(2)以上时,PFOS 的分解并没有增加。在 10 mA/cm(2)的电流密度下,电化学处理 PFOA 和 PFOS 的归一化电流密度和处理体积的一级反应速率常数分别为 46×10(-5)和 70×10(-5) [(min(-1)) (mA/cm(2))(-1) (L)]。确认了 PFOA 和 PFOS 的脱氟反应,分别有 58%和 98%的氟化物回收(基于降解的 PFOA 和 PFOS 的质量)。还观察到了地下水中其他 PFAAs 的处理,短链 PFAAs 通常更难降解。结果突出了电化学处理 AFFF 污染地下水中 PFAAs(特别是 PFOA 和 PFOS)的潜力。

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