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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Pannipa Wongkrua | en_US |
dc.contributor.author | Titipun Thongtem | en_US |
dc.contributor.author | Somchai Thongtem | en_US |
dc.date.accessioned | 2018-09-04T09:29:32Z | - |
dc.date.available | 2018-09-04T09:29:32Z | - |
dc.date.issued | 2013-09-03 | en_US |
dc.identifier.issn | 16874129 | en_US |
dc.identifier.issn | 16874110 | en_US |
dc.identifier.other | 2-s2.0-84883179373 | en_US |
dc.identifier.other | 10.1155/2013/702679 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84883179373&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/52668 | - |
dc.description.abstract | Hexagonal molybdenum oxide (h-MoO3) nano- and microrods were successfully synthesized by refluxing of (NH4)6Mo7O24·4H2O solutions with the pH 1 at 90°C for 1, 3, 5, and 7 h and were further transformed into orthorhombic molybdenum oxide (α-MoO3) microplates by calcination at 450°C for 6 h. These selected products were used to determine the degradation of methylene blue dye under 35 W xenon lamp for 0-180 min, due to the photocatalysis and photosensitization processes. In this research, catalytic activity of the metastable h-MoO3has higher efficiency than that of the thermodynamically stable α-MoO3. Their phase and morphology transformation was also explained according to the experimental results. © 2013 Pannipa Wongkrua et al. | en_US |
dc.subject | Materials Science | en_US |
dc.title | Synthesis of h- and α -MoO3 by refluxing and calcination combination: Phase and morphology transformation, photocatalysis, and photosensitization | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Journal of Nanomaterials | en_US |
article.volume | 2013 | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
Appears in Collections: | CMUL: Journal Articles |
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