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Enhanced degradation of micropollutants using In situ electrogenerated sulfate radical at high flux.

Authors :
Zhou Z
Zheng W
Ji S
Nanayakkara N
Liu Y
Source :
Chemosphere [Chemosphere] 2024 Oct; Vol. 366, pp. 143418. Date of Electronic Publication: 2024 Sep 26.
Publication Year :
2024

Abstract

The degradation of micropollutants via in situ-generated reactive species from coexisting substances in water is a promising approach for advanced water treatment. However, treatment efficiency and practical applications are hindered by limited operation conditions and prohibitive costs, respectively. Herein, we report an upgraded electrochemical filtration system that is chemical-free and made efficient by achieving in situ SO <subscript>4</subscript> <superscript>•-</superscript> generation at enhanced flux and in complicated water matrices. The ion transport was enhanced by coupled electric and flow fields, providing an outstanding performance in removing micropollutants. At the optimized conditions, the proposed system degraded 90.5% of bisphenol A (BPA) in 40 min and its degradation kinetics was 14.7 times that of the batch mode, and the treatment efficiency of the proposed system was 2.5 times more efficient than our previous design because of the enhanced flux. Quenching experiments indicate that indirect oxidation by SO <subscript>4</subscript> <superscript>•</superscript> <superscript>-</superscript> and <superscript>•</superscript> OH as well as direct electron transfer play critical roles during the BPA degradation. Importantly, the proposed system does not need any added chemicals and uses only the ubiquitous SO <subscript>4</subscript> <superscript>2-</superscript> and electricity. From an environmental point of view, its energy conservation and the lack of additional chemicals ensure its applicability for purifying micropollutants.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1879-1298
Volume :
366
Database :
MEDLINE
Journal :
Chemosphere
Publication Type :
Academic Journal
Accession number :
39341390
Full Text :
https://doi.org/10.1016/j.chemosphere.2024.143418