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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...

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Autores principales: Sutyak, Keith B., Iezzi, Erick B., Daniels, Grant C., Camerino, Eugene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
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.
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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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