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Controlled Allocation of Aromatic/Aliphatic Substituents to Polysaccharides and Lignin in Sugarcane Bagasse via Successive Homogeneous Transesterification Using Ionic Liquid

[Image: see text] Lignocellulosic agricultural waste is an abundant renewable feedstock that can be utilized as a sustainable source of biomass-based plastics. Ideally, it is used without discarding any components, including cellulose, hemicellulose, and lignin. However, their utilization as lignoce...

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Autores principales: Suzuki, Shiori, Hamano, Yosuke, Wada, Naoki, Takahashi, Kenji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10233695/
https://www.ncbi.nlm.nih.gov/pubmed/37273610
http://dx.doi.org/10.1021/acsomega.3c00369
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author Suzuki, Shiori
Hamano, Yosuke
Wada, Naoki
Takahashi, Kenji
author_facet Suzuki, Shiori
Hamano, Yosuke
Wada, Naoki
Takahashi, Kenji
author_sort Suzuki, Shiori
collection PubMed
description [Image: see text] Lignocellulosic agricultural waste is an abundant renewable feedstock that can be utilized as a sustainable source of biomass-based plastics. Ideally, it is used without discarding any components, including cellulose, hemicellulose, and lignin. However, their utilization as lignocellulose-based plastics has been limited because of the low compatibility between the polysaccharides and lignin derivatives and the resulting poor mechanical properties of the final products. Here, we demonstrate a facile but highly controllable conversion of sugarcane bagasse into valuable thermoplastics by utilizing the excellent solubility and unique organocatalytic abilities of an ionic liquid, 1-ethyl-3-methylimidazolium acetate. In a homogeneous and one-pot chemical modification reaction system, the substitution ratio of an aromatic benzoyl group to an aliphatic hexanoyl group in the bagasse derivative was adjusted by the ratio of acyl reagents used. Moreover, the allocation of these two acyl groups to polysaccharide and lignin components in bagasse was successfully controlled only by exchanging the order of the acyl reagents introduced into the reaction system. The controlled introduction of the acyl groups into bagasse achieved a homogeneous polymer phase in the resultant multicomponent hot-pressed film, resulting in enhanced mechanical properties such as sufficient tensile strength (∼20 MPa) and excellent ductility with a high strain energy density (∼5 MJ m(–3)).
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spelling pubmed-102336952023-06-02 Controlled Allocation of Aromatic/Aliphatic Substituents to Polysaccharides and Lignin in Sugarcane Bagasse via Successive Homogeneous Transesterification Using Ionic Liquid Suzuki, Shiori Hamano, Yosuke Wada, Naoki Takahashi, Kenji ACS Omega [Image: see text] Lignocellulosic agricultural waste is an abundant renewable feedstock that can be utilized as a sustainable source of biomass-based plastics. Ideally, it is used without discarding any components, including cellulose, hemicellulose, and lignin. However, their utilization as lignocellulose-based plastics has been limited because of the low compatibility between the polysaccharides and lignin derivatives and the resulting poor mechanical properties of the final products. Here, we demonstrate a facile but highly controllable conversion of sugarcane bagasse into valuable thermoplastics by utilizing the excellent solubility and unique organocatalytic abilities of an ionic liquid, 1-ethyl-3-methylimidazolium acetate. In a homogeneous and one-pot chemical modification reaction system, the substitution ratio of an aromatic benzoyl group to an aliphatic hexanoyl group in the bagasse derivative was adjusted by the ratio of acyl reagents used. Moreover, the allocation of these two acyl groups to polysaccharide and lignin components in bagasse was successfully controlled only by exchanging the order of the acyl reagents introduced into the reaction system. The controlled introduction of the acyl groups into bagasse achieved a homogeneous polymer phase in the resultant multicomponent hot-pressed film, resulting in enhanced mechanical properties such as sufficient tensile strength (∼20 MPa) and excellent ductility with a high strain energy density (∼5 MJ m(–3)). American Chemical Society 2023-05-15 /pmc/articles/PMC10233695/ /pubmed/37273610 http://dx.doi.org/10.1021/acsomega.3c00369 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Suzuki, Shiori
Hamano, Yosuke
Wada, Naoki
Takahashi, Kenji
Controlled Allocation of Aromatic/Aliphatic Substituents to Polysaccharides and Lignin in Sugarcane Bagasse via Successive Homogeneous Transesterification Using Ionic Liquid
title Controlled Allocation of Aromatic/Aliphatic Substituents to Polysaccharides and Lignin in Sugarcane Bagasse via Successive Homogeneous Transesterification Using Ionic Liquid
title_full Controlled Allocation of Aromatic/Aliphatic Substituents to Polysaccharides and Lignin in Sugarcane Bagasse via Successive Homogeneous Transesterification Using Ionic Liquid
title_fullStr Controlled Allocation of Aromatic/Aliphatic Substituents to Polysaccharides and Lignin in Sugarcane Bagasse via Successive Homogeneous Transesterification Using Ionic Liquid
title_full_unstemmed Controlled Allocation of Aromatic/Aliphatic Substituents to Polysaccharides and Lignin in Sugarcane Bagasse via Successive Homogeneous Transesterification Using Ionic Liquid
title_short Controlled Allocation of Aromatic/Aliphatic Substituents to Polysaccharides and Lignin in Sugarcane Bagasse via Successive Homogeneous Transesterification Using Ionic Liquid
title_sort controlled allocation of aromatic/aliphatic substituents to polysaccharides and lignin in sugarcane bagasse via successive homogeneous transesterification using ionic liquid
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10233695/
https://www.ncbi.nlm.nih.gov/pubmed/37273610
http://dx.doi.org/10.1021/acsomega.3c00369
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