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Adsorption and Photodegradation Efficiency of TiO2/Fe2O3/PAC and TiO2/Fe2O3/Zeolite Nanophotocatalysts for the Removal of Cyanide

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dc.contributor.authorEskandari, Parisa-
dc.contributor.authorFarhadian, Mehrdad-
dc.contributor.authorNazar, Ali Reza Solaimany-
dc.contributor.authorJeon, Byong Hun-
dc.date.accessioned2022-07-10T09:45:04Z-
dc.date.available2022-07-10T09:45:04Z-
dc.date.created2021-05-12-
dc.date.issued2019-02-
dc.identifier.issn0888-5885-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/148388-
dc.description.abstractThe synthesized TiO2/Fe2O3 nanostructures supported on powder-activated carbon (PAC) and zeolite at different mole ratios of Fe3+/TiO2 were characterized by XRD, XRF, FESEM, EDX, TEM, FTIR, BET, and, PL analyses and their cyanide photodegradation mechanism was thoroughly discussed. The results confirmed not only TiO2/Fe2O3/PAC had higher photocatalytic and adsorption capability but also better structural stability and reusability for cyanide removal than TiO2/Fe2O3/zeolite. The first-order kinetics model indicated that the photodegradation rate using TiO2/Fe2O3/PAC was 1.3 times higher than that of TiO2/Fe2O3/zeolite. The response surface methodology (RSM) assessment showed that pH, irradiation time and initial cyanide concentration using UV/H2O2/TiO2/Fe2O3/zeolite system had more effects on the degradation, respectively; whereas the effectiveness of UV/H2O2/TiO2/Fe2O3/PAC process was highly influenced by initial cyanide concentration than the other two parameters. High R-2 and well-fitted residual plots approved the accuracy of the models in predicting the cyanide degradation efficiency using both the photocatalysts.-
dc.language영어-
dc.language.isoen-
dc.publisherAMER CHEMICAL SOC-
dc.titleAdsorption and Photodegradation Efficiency of TiO2/Fe2O3/PAC and TiO2/Fe2O3/Zeolite Nanophotocatalysts for the Removal of Cyanide-
dc.typeArticle-
dc.contributor.affiliatedAuthorJeon, Byong Hun-
dc.identifier.doi10.1021/acs.iecr.8b05073-
dc.identifier.scopusid2-s2.0-85060779002-
dc.identifier.wosid000458348200029-
dc.identifier.bibliographicCitationINDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, v.58, no.5, pp.2099 - 2112-
dc.relation.isPartOfINDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH-
dc.citation.titleINDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH-
dc.citation.volume58-
dc.citation.number5-
dc.citation.startPage2099-
dc.citation.endPage2112-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.subject.keywordPlusRESPONSE-SURFACE METHODOLOGY-
dc.subject.keywordPlusADVANCED OXIDATION PROCESSES-
dc.subject.keywordPlusPHOTOCATALYTIC DEGRADATION-
dc.subject.keywordPlusAQUEOUS-SOLUTION-
dc.subject.keywordPlusFE2O3/TIO2 NANOPARTICLES-
dc.subject.keywordPlusACTIVATED CARBON-
dc.subject.keywordPlusWATER-TREATMENT-
dc.subject.keywordPlusMETHYL-ORANGE-
dc.subject.keywordPlusWASTE-WATER-
dc.subject.keywordPlusTIO2-
dc.identifier.urlhttps://pubs.acs.org/doi/10.1021/acs.iecr.8b05073-
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