Volume 12, Issue 1 pp. 435-436
Section 8
Free Access

Viscoelastic effects and shrinkage as accompanying phenomena of the curing of polymers. Single- and multiscale effects

Sandra Klinge

Corresponding Author

Sandra Klinge

Institute of Mechanics, University of Bochum, D-44780 Bochum, Germany

phone +49 234 322 6552, fax +49 234 321 4154Search for more papers by this author
Alexander Bartels

Alexander Bartels

Institute of Mechanics, TU-Dortmund, D-44227 Dortmund, Germany

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Klaus Hackl

Klaus Hackl

Institute of Mechanics, University of Bochum, D-44780 Bochum, Germany

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Paul Steinmann

Paul Steinmann

Chair of Applied Mechanics, University of Erlangen-Nürnberg, D-91058 Erlangen, Germany

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First published: 03 December 2012

Abstract

The contribution deals with the modeling of two phenomena that are characteristic of the curing of polymers, namely the increasing viscosity and the volume decrease known as autogeneous shrinkage. Both of these processes are caused by the crosslinking of polymer chains during polymerization. In order to model the viscoelastic effects, the free energy consisting of an equilibrium and a non-equilibrium part is proposed. The former is related to the elastic processes and depends on total deformations. The latter is caused by the viscoelastic effects and only depends on the elastic part of deformations. In order to avoid volume locking effects typical of isochoric materials, both parts of the free energy density are furthermore split into a volumetric and a deviatoric part. A multifield description depending on the displacements, volume change and hydrostatic pressure is introduced as well. Different from the viscous process, the modeling of shrinkage effects does not require a new assumption for the free energy but a split of the total deformation gradient into a shrinkage and a mechanical part. The model suitable for simulating both of the mentioned phenomena is implemented in the single- and multiscale FE program. (© 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim)

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