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Hydrolytically Stable and Thermo-Mechanically Tunable Poly(Urethane) Thermoset Networks that Selectively Degrade and Generate Reusable Molecules
[Image: see text] Cross-linked polymeric networks that possess tunable properties and degrade on-demand have broad applications in today’s society. Herein, we report on silyl-containing poly(urethane) (silyl-PU) thermoset networks, which are highly cross-linked stimuli-responsive materials with hydr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9242536/ https://www.ncbi.nlm.nih.gov/pubmed/35503369 http://dx.doi.org/10.1021/acsami.2c00485 |
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author | Sutyak, Keith B. Iezzi, Erick B. Daniels, Grant C. Camerino, Eugene |
author_facet | Sutyak, Keith B. Iezzi, Erick B. Daniels, Grant C. Camerino, Eugene |
author_sort | Sutyak, Keith B. |
collection | PubMed |
description | [Image: see text] Cross-linked polymeric networks that possess tunable properties and degrade on-demand have broad applications in today’s society. Herein, we report on silyl-containing poly(urethane) (silyl-PU) thermoset networks, which are highly cross-linked stimuli-responsive materials with hydrolytic stability at 37.7 °C and 95% relative humidity, thermal stability of 280–311.2 °C, tensile properties of 0.38–51.7 MPa strength and 73.7–256.4% elongation, including storage modulus of 2268–3499 MPa (in the glassy state). However, unlike traditional (i.e., nondegradable) PU thermosets, these silyl-PUs selectively activate with fluoride ion under mild and static conditions to completely degrade, via cascading bond cleavages, and generate recoverable and reusable molecules. Silyl-PUs, as thin films, also demonstrated complete removal (within 30 min) from a strongly adhered epoxy thermoset network without altering the structure of the latter. Silyl-PU thermosets have potential applications in composite parts, vehicle and industrial coatings, and rigid plastics for personal devices, and may reduce environmental waste compared to nondegradable, single-use materials. |
format | Online Article Text |
id | pubmed-9242536 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-92425362022-06-30 Hydrolytically Stable and Thermo-Mechanically Tunable Poly(Urethane) Thermoset Networks that Selectively Degrade and Generate Reusable Molecules Sutyak, Keith B. Iezzi, Erick B. Daniels, Grant C. Camerino, Eugene ACS Appl Mater Interfaces [Image: see text] Cross-linked polymeric networks that possess tunable properties and degrade on-demand have broad applications in today’s society. Herein, we report on silyl-containing poly(urethane) (silyl-PU) thermoset networks, which are highly cross-linked stimuli-responsive materials with hydrolytic stability at 37.7 °C and 95% relative humidity, thermal stability of 280–311.2 °C, tensile properties of 0.38–51.7 MPa strength and 73.7–256.4% elongation, including storage modulus of 2268–3499 MPa (in the glassy state). However, unlike traditional (i.e., nondegradable) PU thermosets, these silyl-PUs selectively activate with fluoride ion under mild and static conditions to completely degrade, via cascading bond cleavages, and generate recoverable and reusable molecules. Silyl-PUs, as thin films, also demonstrated complete removal (within 30 min) from a strongly adhered epoxy thermoset network without altering the structure of the latter. Silyl-PU thermosets have potential applications in composite parts, vehicle and industrial coatings, and rigid plastics for personal devices, and may reduce environmental waste compared to nondegradable, single-use materials. American Chemical Society 2022-05-03 2022-05-18 /pmc/articles/PMC9242536/ /pubmed/35503369 http://dx.doi.org/10.1021/acsami.2c00485 Text en Not subject to U.S. Copyright. Published 2022 by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Sutyak, Keith B. Iezzi, Erick B. Daniels, Grant C. Camerino, Eugene Hydrolytically Stable and Thermo-Mechanically Tunable Poly(Urethane) Thermoset Networks that Selectively Degrade and Generate Reusable Molecules |
title | Hydrolytically
Stable and Thermo-Mechanically Tunable
Poly(Urethane) Thermoset Networks that Selectively Degrade and Generate
Reusable Molecules |
title_full | Hydrolytically
Stable and Thermo-Mechanically Tunable
Poly(Urethane) Thermoset Networks that Selectively Degrade and Generate
Reusable Molecules |
title_fullStr | Hydrolytically
Stable and Thermo-Mechanically Tunable
Poly(Urethane) Thermoset Networks that Selectively Degrade and Generate
Reusable Molecules |
title_full_unstemmed | Hydrolytically
Stable and Thermo-Mechanically Tunable
Poly(Urethane) Thermoset Networks that Selectively Degrade and Generate
Reusable Molecules |
title_short | Hydrolytically
Stable and Thermo-Mechanically Tunable
Poly(Urethane) Thermoset Networks that Selectively Degrade and Generate
Reusable Molecules |
title_sort | hydrolytically
stable and thermo-mechanically tunable
poly(urethane) thermoset networks that selectively degrade and generate
reusable molecules |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9242536/ https://www.ncbi.nlm.nih.gov/pubmed/35503369 http://dx.doi.org/10.1021/acsami.2c00485 |
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