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...
Saved in:
Main Authors: | , , , , , |
---|---|
Format: | Journal |
Published: |
2018
|
Subjects: | |
Online Access: | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33747445057&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/61509 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Chiang Mai University |
id |
th-cmuir.6653943832-61509 |
---|---|
record_format |
dspace |
spelling |
th-cmuir.6653943832-615092018-09-11T09:01:39Z Electrocoagulation of quinone pigments Neeranuch Chairungsi Kanlaya Jumpatong Patiwat Suebsakwong Waya Sengpracha Weerachai Phutdhawong Duang Buddhasukh Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics 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. 2018-09-11T08:54:25Z 2018-09-11T08:54:25Z 2006-08-24 Journal 14203049 14203049 2-s2.0-33747445057 10.3390/11070514 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33747445057&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/61509 |
institution |
Chiang Mai University |
building |
Chiang Mai University Library |
country |
Thailand |
collection |
CMU Intellectual Repository |
topic |
Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics |
spellingShingle |
Biochemistry, Genetics and Molecular Biology Chemistry Pharmacology, Toxicology and Pharmaceutics Neeranuch Chairungsi Kanlaya Jumpatong Patiwat Suebsakwong Waya Sengpracha Weerachai Phutdhawong Duang Buddhasukh Electrocoagulation of quinone pigments |
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 |
Journal |
author |
Neeranuch Chairungsi Kanlaya Jumpatong Patiwat Suebsakwong Waya Sengpracha Weerachai Phutdhawong Duang Buddhasukh |
author_facet |
Neeranuch Chairungsi Kanlaya Jumpatong Patiwat Suebsakwong Waya Sengpracha Weerachai Phutdhawong Duang Buddhasukh |
author_sort |
Neeranuch Chairungsi |
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 |
2018 |
url |
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33747445057&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/61509 |
_version_ |
1681425634057781248 |