Entropy-driven thermo-gelling vitrimer
Thermo-gelling polymers have been envisioned as promising smart biomaterials but limited by their weak mechanical and thermodynamic stabilities. Here, we propose a new thermo-gelling vitrimer, which remains at a liquid state because of the addition of protector molecules preventing the crosslinking,...
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sg-ntu-dr.10356-1637212023-02-28T20:05:57Z Entropy-driven thermo-gelling vitrimer Xia, Xiuyang Rao, Peilin Yang, Juan Ciamarra, Massimo Pica Ni, Ran School of Chemical and Biomedical Engineering School of Physical and Mathematical Sciences Science::Chemistry Vitrimer Entropy-Driven Crosslinking Thermo-gelling polymers have been envisioned as promising smart biomaterials but limited by their weak mechanical and thermodynamic stabilities. Here, we propose a new thermo-gelling vitrimer, which remains at a liquid state because of the addition of protector molecules preventing the crosslinking, and with increasing temperature, an entropy-driven crosslinking occurs to induce the sol-gel transition. Moreover, we find that the activation barrier in the metathesis reaction of vitrimers plays an important role, and experimentally, one can use catalysts to tune the activation barrier to drive the vitrimer to form an equilibrium gel at high temperature, which is not subject to any thermodynamic instability. We formulate a mean-field theory to describe the entropy-driven crosslinking of the vitrimer, which agrees quantitatively with computer simulations and paves the way for the design and fabrication of novel vitrimers for biomedical applications. Ministry of Education (MOE) Published version This work is supported by the Academic Research Fund from the Singapore Ministry of Education Tier 1 Gant (RG59/21) and Tier 2 Grant (MOE2019-T2-2-010). 2022-12-15T01:58:57Z 2022-12-15T01:58:57Z 2022 Journal Article Xia, X., Rao, P., Yang, J., Ciamarra, M. P. & Ni, R. (2022). Entropy-driven thermo-gelling vitrimer. JACS Au, 2(10), 2359-2366. https://dx.doi.org/10.1021/jacsau.2c00425 2691-3704 https://hdl.handle.net/10356/163721 10.1021/jacsau.2c00425 36311840 2-s2.0-85139551352 10 2 2359 2366 en RG59/21 MOE2019-T2-2-010 JACS Au © 2022 The Authors. Published by American Chemical Society. This is an open-access article distributed under the terms of the Creative Commons Attribution License. application/pdf |
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Science::Chemistry Vitrimer Entropy-Driven Crosslinking Xia, Xiuyang Rao, Peilin Yang, Juan Ciamarra, Massimo Pica Ni, Ran Entropy-driven thermo-gelling vitrimer |
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Thermo-gelling polymers have been envisioned as promising smart biomaterials but limited by their weak mechanical and thermodynamic stabilities. Here, we propose a new thermo-gelling vitrimer, which remains at a liquid state because of the addition of protector molecules preventing the crosslinking, and with increasing temperature, an entropy-driven crosslinking occurs to induce the sol-gel transition. Moreover, we find that the activation barrier in the metathesis reaction of vitrimers plays an important role, and experimentally, one can use catalysts to tune the activation barrier to drive the vitrimer to form an equilibrium gel at high temperature, which is not subject to any thermodynamic instability. We formulate a mean-field theory to describe the entropy-driven crosslinking of the vitrimer, which agrees quantitatively with computer simulations and paves the way for the design and fabrication of novel vitrimers for biomedical applications. |
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School of Chemical and Biomedical Engineering |
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School of Chemical and Biomedical Engineering Xia, Xiuyang Rao, Peilin Yang, Juan Ciamarra, Massimo Pica Ni, Ran |
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Article |
author |
Xia, Xiuyang Rao, Peilin Yang, Juan Ciamarra, Massimo Pica Ni, Ran |
author_sort |
Xia, Xiuyang |
title |
Entropy-driven thermo-gelling vitrimer |
title_short |
Entropy-driven thermo-gelling vitrimer |
title_full |
Entropy-driven thermo-gelling vitrimer |
title_fullStr |
Entropy-driven thermo-gelling vitrimer |
title_full_unstemmed |
Entropy-driven thermo-gelling vitrimer |
title_sort |
entropy-driven thermo-gelling vitrimer |
publishDate |
2022 |
url |
https://hdl.handle.net/10356/163721 |
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