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dc.contributor.authorNeeranuch Chairungsien_US
dc.contributor.authorKanlaya Jumpatongen_US
dc.contributor.authorPatiwat Suebsakwongen_US
dc.contributor.authorWaya Sengprachaen_US
dc.contributor.authorWeerachai Phutdhawongen_US
dc.contributor.authorDuang Buddhasukhen_US
dc.date.accessioned2018-09-11T08:54:25Z-
dc.date.available2018-09-11T08:54:25Z-
dc.date.issued2006-08-24en_US
dc.identifier.issn14203049en_US
dc.identifier.issn14203049en_US
dc.identifier.other2-s2.0-33747445057en_US
dc.identifier.other10.3390/11070514en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33747445057&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/61509-
dc.description.abstractSome 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.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleElectrocoagulation of quinone pigmentsen_US
dc.typeJournalen_US
article.title.sourcetitleMoleculesen_US
article.volume11en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsMaejo Universityen_US
article.stream.affiliationsSilpakorn Universityen_US
Appears in Collections:CMUL: Journal Articles

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