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Article: Enhancement of H2O2 Decomposition by the Co-catalytic Effect of WS2 on the Fenton Reaction for the Synchronous Reduction of Cr(VI) and Remediation of Phenol

TitleEnhancement of H<inf>2</inf>O<inf>2</inf> Decomposition by the Co-catalytic Effect of WS<inf>2</inf> on the Fenton Reaction for the Synchronous Reduction of Cr(VI) and Remediation of Phenol
Authors
Issue Date2018
Citation
Environmental Science and Technology, 2018, v. 52, n. 19, p. 11297-11308 How to Cite?
AbstractThe greatest problem in the Fe(II)/H2O2 Fenton reaction is the low production of ·OH owing to the inefficient Fe(III)/Fe(II) cycle and the low decomposition efficiency of H2O2 (<30%). Herein, we report a new discovery regarding the significant co-catalytic effect of WS2 on the decomposition of H2O2 in a photoassisted Fe(II)/H2O2 Fenton system. With the help of WS2 co-catalytic effect, the H2O2 decomposition efficiency can be increased from 22.9% to 60.1%, such that minimal concentrations of H2O2 (0.4 mmol/L) and Fe2+ (0.14 mmol/L) are necessary for the standard Fenton reaction. Interestingly, the co-catalytic Fenton strategy can be applied to the simultaneous oxidation of phenol (10 mg/L) and reduction of Cr(VI) (40 mg/L), and the corresponding degradation and reduction rates can reach up to 80.9% and 90.9%, respectively, which are much higher than the conventional Fenton reaction (52.0% and 31.0%). We found that the expose reductive W4+ active sites on the surface of WS2 can greatly accelerate the rate-limiting step of Fe3+/Fe2+ conversion, which plays the key role in the decomposition of H2O2 and the reduction of Cr(VI). Our discovery represents a breakthrough in the field of inorganic catalyzing AOPs and greatly advances the practical utility of this method for environmental applications.
Persistent Identifierhttp://hdl.handle.net/10722/341236
ISSN
2021 Impact Factor: 11.357
2020 SCImago Journal Rankings: 2.851
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorDong, Chencheng-
dc.contributor.authorJi, Jiahui-
dc.contributor.authorShen, Bin-
dc.contributor.authorXing, Mingyang-
dc.contributor.authorZhang, Jinlong-
dc.date.accessioned2024-03-13T08:41:14Z-
dc.date.available2024-03-13T08:41:14Z-
dc.date.issued2018-
dc.identifier.citationEnvironmental Science and Technology, 2018, v. 52, n. 19, p. 11297-11308-
dc.identifier.issn0013-936X-
dc.identifier.urihttp://hdl.handle.net/10722/341236-
dc.description.abstractThe greatest problem in the Fe(II)/H2O2 Fenton reaction is the low production of ·OH owing to the inefficient Fe(III)/Fe(II) cycle and the low decomposition efficiency of H2O2 (<30%). Herein, we report a new discovery regarding the significant co-catalytic effect of WS2 on the decomposition of H2O2 in a photoassisted Fe(II)/H2O2 Fenton system. With the help of WS2 co-catalytic effect, the H2O2 decomposition efficiency can be increased from 22.9% to 60.1%, such that minimal concentrations of H2O2 (0.4 mmol/L) and Fe2+ (0.14 mmol/L) are necessary for the standard Fenton reaction. Interestingly, the co-catalytic Fenton strategy can be applied to the simultaneous oxidation of phenol (10 mg/L) and reduction of Cr(VI) (40 mg/L), and the corresponding degradation and reduction rates can reach up to 80.9% and 90.9%, respectively, which are much higher than the conventional Fenton reaction (52.0% and 31.0%). We found that the expose reductive W4+ active sites on the surface of WS2 can greatly accelerate the rate-limiting step of Fe3+/Fe2+ conversion, which plays the key role in the decomposition of H2O2 and the reduction of Cr(VI). Our discovery represents a breakthrough in the field of inorganic catalyzing AOPs and greatly advances the practical utility of this method for environmental applications.-
dc.languageeng-
dc.relation.ispartofEnvironmental Science and Technology-
dc.titleEnhancement of H<inf>2</inf>O<inf>2</inf> Decomposition by the Co-catalytic Effect of WS<inf>2</inf> on the Fenton Reaction for the Synchronous Reduction of Cr(VI) and Remediation of Phenol-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/acs.est.8b02403-
dc.identifier.pmid30180549-
dc.identifier.scopuseid_2-s2.0-85053828604-
dc.identifier.volume52-
dc.identifier.issue19-
dc.identifier.spage11297-
dc.identifier.epage11308-
dc.identifier.eissn1520-5851-
dc.identifier.isiWOS:000446542100044-

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