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contributor authorZhang, Haohui
contributor authorDehghany, Mohammad
contributor authorHu, Yuhang
date accessioned2022-02-04T14:12:48Z
date available2022-02-04T14:12:48Z
date copyright2020/04/09/
date issued2020
identifier issn0021-8936
identifier otherjam_87_6_061010.pdf
identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4273194
description abstractPolyelectrolyte (PE) gels consist of crosslinked polymer networks that are grafted with ionizable groups and ionic solution. Many stimuli-responsive gels, including pH-responsive, electric-responsive, and light-responsive ones, are PE gels. Most soft biological components are also PE gels. Due to the increasing scientific interests and applications of PE gels, a comprehensive model is needed. In PE gels, not only solvent, but also ions and other small molecules all diffuse inside, and the flows of the different components are coupled. This phenomenon is called cross-diffusion, meaning the flow of one species is not only driven by its own chemical potential gradient, but also influenced by the flow of other species. In this work, we develop a rigorous nonequilibrium thermodynamics framework to study the coupled deformation and diffusion of the PE gels where cross-diffusion is emphasized and quantified. Specific forms of free energy and kinetic laws are proposed. A finite element method is developed and implemented into abaqus through a user element subroutine. The model is used to simulate the deformation of biological axon and PE gels.The numerical results are compared with experimental data. It is shown that cross-diffusion generates anomalous effects not only on the flux but also on the deformation of PE gels.
publisherThe American Society of Mechanical Engineers (ASME)
titleKinetics of Polyelectrolyte Gels
typeJournal Paper
journal volume87
journal issue6
journal titleJournal of Applied Mechanics
identifier doi10.1115/1.4046737
page61010
treeJournal of Applied Mechanics:;2020:;volume( 087 ):;issue: 006
contenttypeFulltext


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