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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Neeranuch Chairungsi | en_US |
dc.contributor.author | Kanlaya Jumpatong | en_US |
dc.contributor.author | Patiwat Suebsakwong | en_US |
dc.contributor.author | Waya Sengpracha | en_US |
dc.contributor.author | Weerachai Phutdhawong | en_US |
dc.contributor.author | Duang Buddhasukh | en_US |
dc.date.accessioned | 2018-09-11T08:54:25Z | - |
dc.date.available | 2018-09-11T08:54:25Z | - |
dc.date.issued | 2006-08-24 | en_US |
dc.identifier.issn | 14203049 | en_US |
dc.identifier.issn | 14203049 | en_US |
dc.identifier.other | 2-s2.0-33747445057 | en_US |
dc.identifier.other | 10.3390/11070514 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33747445057&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/61509 | - |
dc.description.abstract | Some representative quinones, viz. one naphthoquinone (plumbagin) and five anthraquinones (alizarin, purpurin, chrysazin, emodin, and anthrarufin), were subjected to electrocoagulation. It was found that the rate and extent of coagulation of these compounds appears to correlate with the number and relative position of their phenolic substituent groups, and that all of the coagulated quinones could be recovered. Attempts were then made to electrochemically isolate three quinones, namely plumbagin, morindone and erythrolaccin, from natural sources. © 2006 by MDPI. | en_US |
dc.subject | Biochemistry, Genetics and Molecular Biology | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Pharmacology, Toxicology and Pharmaceutics | en_US |
dc.title | Electrocoagulation of quinone pigments | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Molecules | en_US |
article.volume | 11 | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
article.stream.affiliations | Maejo University | en_US |
article.stream.affiliations | Silpakorn University | en_US |
Appears in Collections: | CMUL: Journal Articles |
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