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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...

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Autores principales: Suzuki, Shiori, Shibata, Yoshiki, Hirose, Daisuke, Endo, Takatsugu, Ninomiya, Kazuaki, Kakuchi, Ryohei, Takahashi, Kenji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
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.
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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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