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dc.contributor.authorAnukorn Phuruangraten_US
dc.contributor.authorPhattranit Dumrongrojthanathen_US
dc.contributor.authorNuengruethai Ekthammathaten_US
dc.contributor.authorSomchai Thongtemen_US
dc.contributor.authorTitipun Thongtemen_US
dc.date.accessioned2018-09-04T09:54:24Z-
dc.date.available2018-09-04T09:54:24Z-
dc.date.issued2014-01-01en_US
dc.identifier.issn16874129en_US
dc.identifier.issn16874110en_US
dc.identifier.other2-s2.0-84901747100en_US
dc.identifier.other10.1155/2014/138561en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84901747100&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/53654-
dc.description.abstractIn this research, the effects on reaction temperature and length of time on Bi2WO6nanoplates by hydrothermal synthesis on morphologies and photocatalytic properties were studied. The products obtained at different reaction temperature and reaction time were characterized by XRD, Raman, FTIR, SEM, and TEM techniques. The photocatalytic properties of the samples were measured by decomposing the rhodamine-B organic dye. XRD pattern was specified as pure orthorhombic well-crystallized Bi2WO6phase for the 180°C and 20 h synthesis. Its FTIR spectrum shows main absorption bands at 400-1000 cm-1, assigned to Bi-O stretching, W-O stretching, and W-O-W bridging stretching modes. SEM and TEM analyses show that the product was composed of nanoplates. Photocatalytic activity of Bi2WO6nanoplates shows the 98.24% degradation of rhodamine-B under the Xe light irradiation within 100 min. © 2014 Anukorn Phuruangrat et al.en_US
dc.subjectMaterials Scienceen_US
dc.titleHydrothermal synthesis, characterization, and visible light-driven photocatalytic properties of Bi<inf>2</inf>WO<inf>6</inf>nanoplatesen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Nanomaterialsen_US
article.volume2014en_US
article.stream.affiliationsPrince of Songkla Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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