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dc.contributor.authorKanlaya Pingmuangen_US
dc.contributor.authorNatda Wetchakunen_US
dc.contributor.authorWiyong Kangwansupamonkonen_US
dc.contributor.authorKontad Ounnunkaden_US
dc.contributor.authorBurapat Inceesungvornen_US
dc.contributor.authorSukon Phanichphanten_US
dc.date.accessioned2018-09-04T09:24:30Z-
dc.date.available2018-09-04T09:24:30Z-
dc.date.issued2013-06-28en_US
dc.identifier.issn1687529Xen_US
dc.identifier.issn1110662Xen_US
dc.identifier.other2-s2.0-84879295611en_US
dc.identifier.other10.1155/2013/943256en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84879295611&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/52388-
dc.description.abstractAu/BiVO4visible-light-driven photocatalysts were synthesized by coprecipitation method in the presence of sodium dodecyl benzene sulfonate (SDBS) as a dispersant. Physical characterization of the obtained materials was carried out by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), UV-Vis diffuse reflectance spectroscopy (DRS) and Brunauer, and Emmett and Teller (BET) specific surface area measurement. Photocatalytic performances of the as-prepared Au/BiVO4have also been evaluated via mineralizations of oxalic acid and malonic acid under visible light irradiation. XRD and SEM results indicated that Au/BiVO4photocatalysts were of almost spherical particles with scheelite-monoclinic phase. Photocatalytic results showed that all Au/BiVO4samples exhibited higher oxalic acid mineralization rate than that of pure BiVO4, probably due to a decrease of BiVO4band gap energy and the presence of surface plasmon absorption upon loading BiVO4with Au as evidenced from UV-Vis DRS results. The nominal Au loading amount of 0.25 mol% provided the highest pseudo-first-order rate constant of 0.0487 min-1and 0.0082 min-1for degradations of oxalic acid (C2) and malonic acid (C3), respectively. By considering structures of the two acids, lower pseudo-first-order rate constantly obtained in the case of malonic acid degradation was likely due to an increased complexity of the degradation mechanism of the longer chain acid. © 2013 Kanlaya Pingmuang et al.en_US
dc.subjectChemistryen_US
dc.subjectEnergyen_US
dc.subjectMaterials Scienceen_US
dc.subjectPhysics and Astronomyen_US
dc.titlePhotocatalytic mineralization of organic acids over visible-light-driven Au/BiVO<inf>4</inf>photocatalysten_US
dc.typeJournalen_US
article.title.sourcetitleInternational Journal of Photoenergyen_US
article.volume2013en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsThailand National Nanotechnology Centeren_US
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