Treatment of perfluoroalkyl acids by heat-activated persulfate under conditions representative of in situ chemical oxidation

被引:116
作者
Bruton, Thomas A. [1 ,2 ]
Sedlak, David L. [1 ]
机构
[1] Univ Calif Berkeley, Dept Civil & Environm Engn, Berkeley, CA 94720 USA
[2] Green Sci Policy Inst, Berkeley, CA USA
关键词
PFOA; PFOS; PFAS; persulfate; In situ chemical oxidation; Remediation; FILM-FORMING FOAM; PERFLUOROOCTANOIC ACID; WATER-TREATMENT; PERFLUOROCARBOXYLIC ACIDS; EFFICIENT DECOMPOSITION; TREATMENT TECHNOLOGIES; SULFATE RADICALS; SUBSTANCES PFASS; PFOA; GROUNDWATER;
D O I
10.1016/j.chemosphere.2018.04.128
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Perfluoroalkyl acids (PFAAs) are a class of organic contaminants notable for their extreme persistence. The unique chemical properties of these compounds make them difficult to remove from water using most standard water treatment techniques. To gain insight into the possibility of remediating contaminated groundwater by in situ chemical oxidation with heat-activated persulfate, PFAA removal and the generation of transformation products were evaluated under laboratory conditions. Solution pH had a strong influence on the removal of perfluorooctanoic acid (PFOA), resulting in its transformation into shorter-chain perfluorocarboxylic acids (PFCAs) at pH values below 3. The presence of chloride and aquifer sediments decreased the efficiency of the process by less than 25% under conditions likely to be encountered in drinking water aquifers. Perfluorooctane sulfonic acid (PFOS) was not transformed by heat-activated persulfate under any of the conditions tested. Despite challenges related to the need to manipulate aquifer pH, the possible generation of undesirable short-chain PFCAs and chlorate, and metals mobilization, heat-activated persulfate may be a useful treatment technology for sites contaminated with PFCAs and fluorotelomer-based compounds, including those used in current-generation aqueous film-forming foams. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:457 / 464
页数:8
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