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Oxygen vacancy modification of commercial ZnO by hydrogen reduction for the removal of thiabendazole: Characterization and kinetic study

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dc.contributor.authorRanjbari, Alireza-
dc.contributor.authorDemeestere, Kristof-
dc.contributor.authorKim, Ki-Hyun-
dc.contributor.authorHeynderickx, Philippe M.-
dc.date.accessioned2023-07-05T02:34:32Z-
dc.date.available2023-07-05T02:34:32Z-
dc.date.created2023-02-08-
dc.date.issued2023-05-
dc.identifier.issn0926-3373-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/186071-
dc.description.abstractThe effect of temperature-programmed H2 reduction on modification of surface oxygen vacancies in commercial ZnO (C-ZnO) is investigated. The photocatalytic degradation of the fungicide thiabendazole was optimized by treating C-ZnO with 10% H2/Ar gas at 500 °C over 5 h. The formation of oxygen vacancies and their catalytic activity were compared before and after the reduction treatment based on their characterization analysis (e.g., TPR, FE-SEM, EDS, XPS, Tauc plot, XRD, and BET). Our most recent kinetic modeling was carried out on the experiments using C-ZnO and T500 at different pH values. The highest adsorption removal and photocatalytic degradation rate (and quantum yield) was occurred at pH 3 and 11, respectively. Good reusability of the optimal reduced catalyst was confirmed when tested over five cycles. A strong compatibility between the kinetic modeling results and all characterization analyses supports the potent role of reduction treatment for the modification of oxygen vacancies on photocatalysis.-
dc.language영어-
dc.language.isoen-
dc.publisherELSEVIER-
dc.titleOxygen vacancy modification of commercial ZnO by hydrogen reduction for the removal of thiabendazole: Characterization and kinetic study-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Ki-Hyun-
dc.identifier.doi10.1016/j.apcatb.2022.122265-
dc.identifier.scopusid2-s2.0-85145707338-
dc.identifier.wosid001007474300001-
dc.identifier.bibliographicCitationAPPLIED CATALYSIS B-ENVIRONMENTAL, v.324, pp.1 - 18-
dc.relation.isPartOfAPPLIED CATALYSIS B-ENVIRONMENTAL-
dc.citation.titleAPPLIED CATALYSIS B-ENVIRONMENTAL-
dc.citation.volume324-
dc.citation.startPage1-
dc.citation.endPage18-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryEngineering, Environmental-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.subject.keywordPlusENHANCED PHOTOCATALYTIC ACTIVITY-
dc.subject.keywordPlusBAND-GAP-
dc.subject.keywordPlusTRANSFORMATION PRODUCTS-
dc.subject.keywordPlusVISIBLE ACTIVITY-
dc.subject.keywordPlusDEGRADATION-
dc.subject.keywordPlusWATER-
dc.subject.keywordPlusTIO2-
dc.subject.keywordPlusSURFACE-
dc.subject.keywordPlusLIGHT-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordAuthorOxygen vacancy-
dc.subject.keywordAuthorPhotocatalysis-
dc.subject.keywordAuthorZnO-
dc.subject.keywordAuthorKinetic modeling-
dc.subject.keywordAuthorAdsorption-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0926337322012061?via%3Dihub-
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