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Reaction Mechanism of Phenolic Lignin and High Concentration Chlorine Dioxide and Its Application
[Image: see text] In fact, the chemical reaction rate of traditional chlorine dioxide bleaching of pulp is too fast to observe the intermediate process. The mechanism behind the reaction of 4-hydroxy-3-methoxyacetophenone (APO), a phenolic lignin model compound, with high concentrations of chlorine...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482299/ https://www.ncbi.nlm.nih.gov/pubmed/32923806 http://dx.doi.org/10.1021/acsomega.0c03028 |
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author | Liu, Baojie Qin, Chengrong Zhang, Fuqiang Wang, Shuo Liang, Chen Nie, Shuangxi Wang, Shuangfei Yao, Shuangquan |
author_facet | Liu, Baojie Qin, Chengrong Zhang, Fuqiang Wang, Shuo Liang, Chen Nie, Shuangxi Wang, Shuangfei Yao, Shuangquan |
author_sort | Liu, Baojie |
collection | PubMed |
description | [Image: see text] In fact, the chemical reaction rate of traditional chlorine dioxide bleaching of pulp is too fast to observe the intermediate process. The mechanism behind the reaction of 4-hydroxy-3-methoxyacetophenone (APO), a phenolic lignin model compound, with high concentrations of chlorine dioxide was investigated. Individual solutions of each compound and a mixture of the two were analyzed by UV–vis spectrophotometry, and an absorbance band at 260 nm was observed for the stable benzoquinone intermediates at room temperature. Free chlorine dioxide displayed an absorbance at 360 nm and changes in this absorbance were studied with different APO concentrations. A fixed molar ratio of 1:3 was obtained between APO and chlorine dioxide consumption. The intermediate absorbance demonstrated a linear relationship with the APO concentration. The reaction path between APO and chlorine dioxide at high concentrations was speculated, and it was observed that the activity of C1, C2, C3, C5, and C6 on the APO benzene ring was enhanced when high concentrations of chlorine dioxide were present. From these results, a new method for efficient and clean chlorine dioxide bleaching can be developed. |
format | Online Article Text |
id | pubmed-7482299 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-74822992020-09-11 Reaction Mechanism of Phenolic Lignin and High Concentration Chlorine Dioxide and Its Application Liu, Baojie Qin, Chengrong Zhang, Fuqiang Wang, Shuo Liang, Chen Nie, Shuangxi Wang, Shuangfei Yao, Shuangquan ACS Omega [Image: see text] In fact, the chemical reaction rate of traditional chlorine dioxide bleaching of pulp is too fast to observe the intermediate process. The mechanism behind the reaction of 4-hydroxy-3-methoxyacetophenone (APO), a phenolic lignin model compound, with high concentrations of chlorine dioxide was investigated. Individual solutions of each compound and a mixture of the two were analyzed by UV–vis spectrophotometry, and an absorbance band at 260 nm was observed for the stable benzoquinone intermediates at room temperature. Free chlorine dioxide displayed an absorbance at 360 nm and changes in this absorbance were studied with different APO concentrations. A fixed molar ratio of 1:3 was obtained between APO and chlorine dioxide consumption. The intermediate absorbance demonstrated a linear relationship with the APO concentration. The reaction path between APO and chlorine dioxide at high concentrations was speculated, and it was observed that the activity of C1, C2, C3, C5, and C6 on the APO benzene ring was enhanced when high concentrations of chlorine dioxide were present. From these results, a new method for efficient and clean chlorine dioxide bleaching can be developed. American Chemical Society 2020-08-25 /pmc/articles/PMC7482299/ /pubmed/32923806 http://dx.doi.org/10.1021/acsomega.0c03028 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Liu, Baojie Qin, Chengrong Zhang, Fuqiang Wang, Shuo Liang, Chen Nie, Shuangxi Wang, Shuangfei Yao, Shuangquan Reaction Mechanism of Phenolic Lignin and High Concentration Chlorine Dioxide and Its Application |
title | Reaction Mechanism of Phenolic Lignin and High Concentration
Chlorine Dioxide and Its Application |
title_full | Reaction Mechanism of Phenolic Lignin and High Concentration
Chlorine Dioxide and Its Application |
title_fullStr | Reaction Mechanism of Phenolic Lignin and High Concentration
Chlorine Dioxide and Its Application |
title_full_unstemmed | Reaction Mechanism of Phenolic Lignin and High Concentration
Chlorine Dioxide and Its Application |
title_short | Reaction Mechanism of Phenolic Lignin and High Concentration
Chlorine Dioxide and Its Application |
title_sort | reaction mechanism of phenolic lignin and high concentration
chlorine dioxide and its application |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482299/ https://www.ncbi.nlm.nih.gov/pubmed/32923806 http://dx.doi.org/10.1021/acsomega.0c03028 |
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