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Microstructure-based hyperelastic models for closed-cell solids

For cellular bodies involving large elastic deformations, mesoscopic continuum models that take into account the interplay between the geometry and the microstructural responses of the constituents are developed, analysed and compared with finite-element simulations of cellular structures with diffe...

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Detalles Bibliográficos
Autores principales: Mihai, L. Angela, Wyatt, Hayley, Goriely, Alain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society Publishing 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5415700/
https://www.ncbi.nlm.nih.gov/pubmed/28484340
http://dx.doi.org/10.1098/rspa.2017.0036
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author Mihai, L. Angela
Wyatt, Hayley
Goriely, Alain
author_facet Mihai, L. Angela
Wyatt, Hayley
Goriely, Alain
author_sort Mihai, L. Angela
collection PubMed
description For cellular bodies involving large elastic deformations, mesoscopic continuum models that take into account the interplay between the geometry and the microstructural responses of the constituents are developed, analysed and compared with finite-element simulations of cellular structures with different architecture. For these models, constitutive restrictions for the physical plausibility of the material responses are established, and global descriptors such as nonlinear elastic and shear moduli and Poisson’s ratio are obtained from the material characteristics of the constituents. Numerical results show that these models capture well the mechanical responses of finite-element simulations for three-dimensional periodic structures of neo-Hookean material with closed cells under large tension. In particular, the mesoscopic models predict the macroscopic stiffening of the structure when the stiffness of the cell-core increases.
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spelling pubmed-54157002017-05-08 Microstructure-based hyperelastic models for closed-cell solids Mihai, L. Angela Wyatt, Hayley Goriely, Alain Proc Math Phys Eng Sci Research Articles For cellular bodies involving large elastic deformations, mesoscopic continuum models that take into account the interplay between the geometry and the microstructural responses of the constituents are developed, analysed and compared with finite-element simulations of cellular structures with different architecture. For these models, constitutive restrictions for the physical plausibility of the material responses are established, and global descriptors such as nonlinear elastic and shear moduli and Poisson’s ratio are obtained from the material characteristics of the constituents. Numerical results show that these models capture well the mechanical responses of finite-element simulations for three-dimensional periodic structures of neo-Hookean material with closed cells under large tension. In particular, the mesoscopic models predict the macroscopic stiffening of the structure when the stiffness of the cell-core increases. The Royal Society Publishing 2017-04 2017-04-05 /pmc/articles/PMC5415700/ /pubmed/28484340 http://dx.doi.org/10.1098/rspa.2017.0036 Text en © 2017 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Research Articles
Mihai, L. Angela
Wyatt, Hayley
Goriely, Alain
Microstructure-based hyperelastic models for closed-cell solids
title Microstructure-based hyperelastic models for closed-cell solids
title_full Microstructure-based hyperelastic models for closed-cell solids
title_fullStr Microstructure-based hyperelastic models for closed-cell solids
title_full_unstemmed Microstructure-based hyperelastic models for closed-cell solids
title_short Microstructure-based hyperelastic models for closed-cell solids
title_sort microstructure-based hyperelastic models for closed-cell solids
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5415700/
https://www.ncbi.nlm.nih.gov/pubmed/28484340
http://dx.doi.org/10.1098/rspa.2017.0036
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