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Cellulose triacetate synthesis via one-pot organocatalytic transesterification and delignification of pretreated bagasse
Cellulose triacetate was synthesised by the transesterification reaction of mild acid-pretreated lignocellulosic biomass with a stable acetylating reagent (isopropenyl acetate, IPA) in an ionic liquid (1-ethyl-3-methylimidazolium acetate, EmimOAc) which enabled the dissolution of lignocellulose as w...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080981/ https://www.ncbi.nlm.nih.gov/pubmed/35541740 http://dx.doi.org/10.1039/c8ra03859g |
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author | Suzuki, Shiori Shibata, Yoshiki Hirose, Daisuke Endo, Takatsugu Ninomiya, Kazuaki Kakuchi, Ryohei Takahashi, Kenji |
author_facet | Suzuki, Shiori Shibata, Yoshiki Hirose, Daisuke Endo, Takatsugu Ninomiya, Kazuaki Kakuchi, Ryohei Takahashi, Kenji |
author_sort | Suzuki, Shiori |
collection | PubMed |
description | Cellulose triacetate was synthesised by the transesterification reaction of mild acid-pretreated lignocellulosic biomass with a stable acetylating reagent (isopropenyl acetate, IPA) in an ionic liquid (1-ethyl-3-methylimidazolium acetate, EmimOAc) which enabled the dissolution of lignocellulose as well as the organocatalytic reaction. The homogeneous acetylation of pretreated sugar-cane bagasse was carried out under mild conditions (80 °C, 30 min), and the subsequent reprecipitation processes led to enriched cellulose triacetate with a high degree of substitution (DS; 2.98) and glucose purity (∼90%) along with production of lignin acetate. |
format | Online Article Text |
id | pubmed-9080981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90809812022-05-09 Cellulose triacetate synthesis via one-pot organocatalytic transesterification and delignification of pretreated bagasse Suzuki, Shiori Shibata, Yoshiki Hirose, Daisuke Endo, Takatsugu Ninomiya, Kazuaki Kakuchi, Ryohei Takahashi, Kenji RSC Adv Chemistry Cellulose triacetate was synthesised by the transesterification reaction of mild acid-pretreated lignocellulosic biomass with a stable acetylating reagent (isopropenyl acetate, IPA) in an ionic liquid (1-ethyl-3-methylimidazolium acetate, EmimOAc) which enabled the dissolution of lignocellulose as well as the organocatalytic reaction. The homogeneous acetylation of pretreated sugar-cane bagasse was carried out under mild conditions (80 °C, 30 min), and the subsequent reprecipitation processes led to enriched cellulose triacetate with a high degree of substitution (DS; 2.98) and glucose purity (∼90%) along with production of lignin acetate. The Royal Society of Chemistry 2018-06-13 /pmc/articles/PMC9080981/ /pubmed/35541740 http://dx.doi.org/10.1039/c8ra03859g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Suzuki, Shiori Shibata, Yoshiki Hirose, Daisuke Endo, Takatsugu Ninomiya, Kazuaki Kakuchi, Ryohei Takahashi, Kenji Cellulose triacetate synthesis via one-pot organocatalytic transesterification and delignification of pretreated bagasse |
title | Cellulose triacetate synthesis via one-pot organocatalytic transesterification and delignification of pretreated bagasse |
title_full | Cellulose triacetate synthesis via one-pot organocatalytic transesterification and delignification of pretreated bagasse |
title_fullStr | Cellulose triacetate synthesis via one-pot organocatalytic transesterification and delignification of pretreated bagasse |
title_full_unstemmed | Cellulose triacetate synthesis via one-pot organocatalytic transesterification and delignification of pretreated bagasse |
title_short | Cellulose triacetate synthesis via one-pot organocatalytic transesterification and delignification of pretreated bagasse |
title_sort | cellulose triacetate synthesis via one-pot organocatalytic transesterification and delignification of pretreated bagasse |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080981/ https://www.ncbi.nlm.nih.gov/pubmed/35541740 http://dx.doi.org/10.1039/c8ra03859g |
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