Electrocoagulation of quinone pigments

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 r...

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Main Authors: Chairungsi N., Jumpatong K., Suebsakwong P., Sengpracha W., Phutdhawong W., Buddhasukh D.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-33747445057&partnerID=40&md5=c7e409a7ce0360a6d7490915ef4e5258
http://www.ncbi.nlm.nih.gov/pubmed/17971722
http://cmuir.cmu.ac.th/handle/6653943832/5088
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-50882014-08-30T02:56:08Z Electrocoagulation of quinone pigments Chairungsi N. Jumpatong K. Suebsakwong P. Sengpracha W. Phutdhawong W. Buddhasukh D. 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. 2014-08-30T02:56:08Z 2014-08-30T02:56:08Z 2006 Article 14203049 10.3390/11070514 17971722 MOLEF http://www.scopus.com/inward/record.url?eid=2-s2.0-33747445057&partnerID=40&md5=c7e409a7ce0360a6d7490915ef4e5258 http://www.ncbi.nlm.nih.gov/pubmed/17971722 http://cmuir.cmu.ac.th/handle/6653943832/5088 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description 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.
format Article
author Chairungsi N.
Jumpatong K.
Suebsakwong P.
Sengpracha W.
Phutdhawong W.
Buddhasukh D.
spellingShingle Chairungsi N.
Jumpatong K.
Suebsakwong P.
Sengpracha W.
Phutdhawong W.
Buddhasukh D.
Electrocoagulation of quinone pigments
author_facet Chairungsi N.
Jumpatong K.
Suebsakwong P.
Sengpracha W.
Phutdhawong W.
Buddhasukh D.
author_sort Chairungsi N.
title Electrocoagulation of quinone pigments
title_short Electrocoagulation of quinone pigments
title_full Electrocoagulation of quinone pigments
title_fullStr Electrocoagulation of quinone pigments
title_full_unstemmed Electrocoagulation of quinone pigments
title_sort electrocoagulation of quinone pigments
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-33747445057&partnerID=40&md5=c7e409a7ce0360a6d7490915ef4e5258
http://www.ncbi.nlm.nih.gov/pubmed/17971722
http://cmuir.cmu.ac.th/handle/6653943832/5088
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