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Utilizing Self‐Floating Cu3BiS3 Polydopamine Polyurethane Sponges for Enhanced Water Purification: Harnessing the free radical and non‐radical in persulfate system

The advanced oxidation process based on persulfate group is a promising technology for water purification. However, the synergistic effect of free radical and non‐free radical degradation is still not feasible in the persulfate activation process, which consumes a large amount of external energy. Th...

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Bibliographic Details
Published in:ChemistrySelect (Weinheim) 2024-01, Vol.9 (4), p.n/a
Main Authors: Xiao, Yi, Zhou, Yi, He, Wanhong, Huang, Guihua, Feng, Dujie, Xiang, Minghui, Dang, Mingming, Zhang, Jin
Format: Article
Language:English
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Summary:The advanced oxidation process based on persulfate group is a promising technology for water purification. However, the synergistic effect of free radical and non‐free radical degradation is still not feasible in the persulfate activation process, which consumes a large amount of external energy. The self‐floating Cu3BiS3/polydopamine/polyurethane sponge was prepared using a simple method, resulting in high catalytic performance when activated by peroxydisulfate (PDS). The experiments conducted to identify free radicals showed that the degradation process of tetracycline (TC) involved the synergistic action of non‐radical 1O2 and free radicals (SO4⋅− and • OH) and the conversion of Cu+/Cu2+. The addition of Cl−, HCO3−, PO43−, and SO42− to the solution did not significantly affect the high degradation rate of TC. Furthermore, the interfacial evaporation process achieved a remarkable evaporation rate of 1.53 kg m−2 h−1 and produced reclaimed water without any detectable TC contaminants. The sponge also exhibited excellent salt resistance and chemical stability. This study provides valuable insights into the degradation of antibiotics and the desalination of seawater. The self‐floating Cu3BiS3/polydopamine/polyurethane sponge, activated by peroxydisulfate (PDS), demonstrates high catalytic performance. Experiments reveal that the degradation of tetracycline (TC) involves the synergistic action of non‐radical 1O2 and free radicals (SO4⋅− and • OH), along with the conversion of Cu+/Cu2+. Additionally, the interfacial evaporation process achieves a remarkable evaporation rate of 1.53 kg m−2 h−1, producing reclaimed water free of detectable TC contaminants.
ISSN:2365-6549
2365-6549
DOI:10.1002/slct.202304966