Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/61509
Title: Electrocoagulation of quinone pigments
Authors: Neeranuch Chairungsi
Kanlaya Jumpatong
Patiwat Suebsakwong
Waya Sengpracha
Weerachai Phutdhawong
Duang Buddhasukh
Authors: Neeranuch Chairungsi
Kanlaya Jumpatong
Patiwat Suebsakwong
Waya Sengpracha
Weerachai Phutdhawong
Duang Buddhasukh
Keywords: Biochemistry, Genetics and Molecular Biology;Chemistry;Pharmacology, Toxicology and Pharmaceutics
Issue Date: 24-Aug-2006
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.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33747445057&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/61509
ISSN: 14203049
14203049
Appears in Collections:CMUL: Journal Articles

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