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Mechanics Underpinning Phase Separation of Hydrogels

[Image: see text] This paper reveals the underpinning role of mechanical constraints and dynamic loading in triggering volume phase transitions and phase separation of hydrogels. Using the Flory–Rehner free energy that does not predict phase separation of hydrogels under equilibrium free swelling, w...

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Detalles Bibliográficos
Autores principales: Zhou, Yu, Jin, Lihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9879212/
https://www.ncbi.nlm.nih.gov/pubmed/36711110
http://dx.doi.org/10.1021/acs.macromol.2c02356
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author Zhou, Yu
Jin, Lihua
author_facet Zhou, Yu
Jin, Lihua
author_sort Zhou, Yu
collection PubMed
description [Image: see text] This paper reveals the underpinning role of mechanical constraints and dynamic loading in triggering volume phase transitions and phase separation of hydrogels. Using the Flory–Rehner free energy that does not predict phase separation of hydrogels under equilibrium free swelling, we show that mechanical constraints can lead to coexistence of multiple phases. We systematically obtain the states of equilibrium for hydrogels under various mechanical constraints and unravel how mechanical constraints change the convexity of the free energy and monotonicity of the stress–stretch curves, leading to phase coexistence. Using a phase-field model, we predict the pattern evolution of phase coexistence and show that many features cannot be captured by the homogeneous states of equilibrium due to large mismatch stretch between the coexisting phases. We further reveal that the system size, quenching rate, and loading rate can significantly influence the phase behavior, which provides insights for experimental studies related to morphological patterns of hydrogels.
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spelling pubmed-98792122023-01-27 Mechanics Underpinning Phase Separation of Hydrogels Zhou, Yu Jin, Lihua Macromolecules [Image: see text] This paper reveals the underpinning role of mechanical constraints and dynamic loading in triggering volume phase transitions and phase separation of hydrogels. Using the Flory–Rehner free energy that does not predict phase separation of hydrogels under equilibrium free swelling, we show that mechanical constraints can lead to coexistence of multiple phases. We systematically obtain the states of equilibrium for hydrogels under various mechanical constraints and unravel how mechanical constraints change the convexity of the free energy and monotonicity of the stress–stretch curves, leading to phase coexistence. Using a phase-field model, we predict the pattern evolution of phase coexistence and show that many features cannot be captured by the homogeneous states of equilibrium due to large mismatch stretch between the coexisting phases. We further reveal that the system size, quenching rate, and loading rate can significantly influence the phase behavior, which provides insights for experimental studies related to morphological patterns of hydrogels. American Chemical Society 2023-01-05 /pmc/articles/PMC9879212/ /pubmed/36711110 http://dx.doi.org/10.1021/acs.macromol.2c02356 Text en © 2023 The Authors. Published 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 Zhou, Yu
Jin, Lihua
Mechanics Underpinning Phase Separation of Hydrogels
title Mechanics Underpinning Phase Separation of Hydrogels
title_full Mechanics Underpinning Phase Separation of Hydrogels
title_fullStr Mechanics Underpinning Phase Separation of Hydrogels
title_full_unstemmed Mechanics Underpinning Phase Separation of Hydrogels
title_short Mechanics Underpinning Phase Separation of Hydrogels
title_sort mechanics underpinning phase separation of hydrogels
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9879212/
https://www.ncbi.nlm.nih.gov/pubmed/36711110
http://dx.doi.org/10.1021/acs.macromol.2c02356
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