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Interphase Engineering of a Cellulose‐Based Carbon Fiber Reinforced Composite by Applying Click Chemistry
Given our possible future dependence on carbon fiber reinforced composites, the introduction of a renewable matrix might be advantageous for the vision of a sustainable world. Cellulose is a superior green candidate and provides exceptional freedom in composite design as the free OH groups can be co...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151626/ https://www.ncbi.nlm.nih.gov/pubmed/30258744 http://dx.doi.org/10.1002/open.201800180 |
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author | Szabó, László Imanishi, Sari Kawashima, Naohiro Hoshino, Rina Hirose, Daisuke Tsukegi, Takayuki Ninomiya, Kazuaki Takahashi, Kenji |
author_facet | Szabó, László Imanishi, Sari Kawashima, Naohiro Hoshino, Rina Hirose, Daisuke Tsukegi, Takayuki Ninomiya, Kazuaki Takahashi, Kenji |
author_sort | Szabó, László |
collection | PubMed |
description | Given our possible future dependence on carbon fiber reinforced composites, the introduction of a renewable matrix might be advantageous for the vision of a sustainable world. Cellulose is a superior green candidate and provides exceptional freedom in composite design as the free OH groups can be conveniently functionalized to give tailor‐made materials. To obtain a high‐performing carbon fiber reinforced cellulose propionate composite, we accurately tailored the interfacial adhesion by invoking click chemistry. The synthetic strategy involved grafting of a phenylacetylene structure onto the carbon fiber surface, onto which O‐acylated 6‐azido‐6‐deoxycellulose and a number of aromatic azides could be covalently attached. Single‐fiber fragmentation tests indicated that the lipophilicity and size of the substituent on the deposited structure played a crucial role in determining molecular entanglement and mechanical interlocking effects, as penetration into the cellulose propionate matrix was of utmost importance. Enhanced interfacial shear strength was obtained for the carbon fiber covalently functionalized with the cellulose derivative. Nevertheless, the greatest increase was observed for the derivative substituted with a compact and highly lipophilic CF(3) substituent. In a broader sense, our study provides a synthetic platform to bind cellulose derivatives to graphitic surfaces and paves the ways towards the preparation of innovative cellulose‐based carbonaceous materials. |
format | Online Article Text |
id | pubmed-6151626 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61516262018-09-26 Interphase Engineering of a Cellulose‐Based Carbon Fiber Reinforced Composite by Applying Click Chemistry Szabó, László Imanishi, Sari Kawashima, Naohiro Hoshino, Rina Hirose, Daisuke Tsukegi, Takayuki Ninomiya, Kazuaki Takahashi, Kenji ChemistryOpen Full Papers Given our possible future dependence on carbon fiber reinforced composites, the introduction of a renewable matrix might be advantageous for the vision of a sustainable world. Cellulose is a superior green candidate and provides exceptional freedom in composite design as the free OH groups can be conveniently functionalized to give tailor‐made materials. To obtain a high‐performing carbon fiber reinforced cellulose propionate composite, we accurately tailored the interfacial adhesion by invoking click chemistry. The synthetic strategy involved grafting of a phenylacetylene structure onto the carbon fiber surface, onto which O‐acylated 6‐azido‐6‐deoxycellulose and a number of aromatic azides could be covalently attached. Single‐fiber fragmentation tests indicated that the lipophilicity and size of the substituent on the deposited structure played a crucial role in determining molecular entanglement and mechanical interlocking effects, as penetration into the cellulose propionate matrix was of utmost importance. Enhanced interfacial shear strength was obtained for the carbon fiber covalently functionalized with the cellulose derivative. Nevertheless, the greatest increase was observed for the derivative substituted with a compact and highly lipophilic CF(3) substituent. In a broader sense, our study provides a synthetic platform to bind cellulose derivatives to graphitic surfaces and paves the ways towards the preparation of innovative cellulose‐based carbonaceous materials. John Wiley and Sons Inc. 2018-09-24 /pmc/articles/PMC6151626/ /pubmed/30258744 http://dx.doi.org/10.1002/open.201800180 Text en © 2018 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Full Papers Szabó, László Imanishi, Sari Kawashima, Naohiro Hoshino, Rina Hirose, Daisuke Tsukegi, Takayuki Ninomiya, Kazuaki Takahashi, Kenji Interphase Engineering of a Cellulose‐Based Carbon Fiber Reinforced Composite by Applying Click Chemistry |
title | Interphase Engineering of a Cellulose‐Based Carbon Fiber Reinforced Composite by Applying Click Chemistry |
title_full | Interphase Engineering of a Cellulose‐Based Carbon Fiber Reinforced Composite by Applying Click Chemistry |
title_fullStr | Interphase Engineering of a Cellulose‐Based Carbon Fiber Reinforced Composite by Applying Click Chemistry |
title_full_unstemmed | Interphase Engineering of a Cellulose‐Based Carbon Fiber Reinforced Composite by Applying Click Chemistry |
title_short | Interphase Engineering of a Cellulose‐Based Carbon Fiber Reinforced Composite by Applying Click Chemistry |
title_sort | interphase engineering of a cellulose‐based carbon fiber reinforced composite by applying click chemistry |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151626/ https://www.ncbi.nlm.nih.gov/pubmed/30258744 http://dx.doi.org/10.1002/open.201800180 |
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