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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kanlaya Pingmuang | en_US |
dc.contributor.author | Natda Wetchakun | en_US |
dc.contributor.author | Wiyong Kangwansupamonkon | en_US |
dc.contributor.author | Kontad Ounnunkad | en_US |
dc.contributor.author | Burapat Inceesungvorn | en_US |
dc.contributor.author | Sukon Phanichphant | en_US |
dc.date.accessioned | 2018-09-04T09:24:30Z | - |
dc.date.available | 2018-09-04T09:24:30Z | - |
dc.date.issued | 2013-06-28 | en_US |
dc.identifier.issn | 1687529X | en_US |
dc.identifier.issn | 1110662X | en_US |
dc.identifier.other | 2-s2.0-84879295611 | en_US |
dc.identifier.other | 10.1155/2013/943256 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84879295611&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/52388 | - |
dc.description.abstract | Au/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.subject | Chemistry | en_US |
dc.subject | Energy | en_US |
dc.subject | Materials Science | en_US |
dc.subject | Physics and Astronomy | en_US |
dc.title | Photocatalytic mineralization of organic acids over visible-light-driven Au/BiVO<inf>4</inf>photocatalyst | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | International Journal of Photoenergy | en_US |
article.volume | 2013 | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
article.stream.affiliations | Thailand National Nanotechnology Center | en_US |
Appears in Collections: | CMUL: Journal Articles |
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