Mechanistic Constitutive Models for Rubber Elasticity and Viscoelasticity

Puso, M

Lawrence Livermore National Laboratory

关键词: Compression;    Polymers;    Implementation;    Elasticity;    Orientation;   

DOI  :  10.2172/15004918
RP-ID  :  UCRL-ID-151578
RP-ID  :  W-7405-ENG-48
RP-ID  :  15004918

美国|英语

来源: UNT Digital Library

【 摘 要 】

Physically based models which describe the finite strain behavior of vulcanized rubber are developed. Constitutive laws for elasticity and viscoelasticity are derived by integrating over orientation space the forces due to each individual polymer chain. A novel scheme is presented which effectively approximates these integrals in terms of strain and strain invariants. In addition, the details involving the implementation of such models into a quasi-static large strain finite element formulation are provided. In order to account for the finite extensibility of a molecular chain, Langevin statistics is used to model the chain response. The classical statistical model of rubber assumes that polymer chains interact only at the chemical crosslinks. It is shown that such model when fitted for uniaxial tension data cannot fit compression or equibiaxial data. A model which incorporates the entanglement interactions of surrounding chains, in addition to the finite extensibility of the chains, is shown to give better predictions than the classical model. The technique used for approximating the orientation space integral was applied to both the classical and entanglement models. A viscoelasticity model based on the force equilibration process as described by Doi and Edwards is developed. An assumed form for the transient force in the chain is postulated. The resulting stress tensor is composed of an elastic and a viscoelastic portion with the elastic stress given by the proposed entanglement model. In order to improve the simulation of experimental data, it was found necessary to include the effect of unattached or dangling polymer chains in the viscoelasticity model. The viscoelastic effect of such chains is the manifestation of a disengagement process. This disengagement model for unattached polymer chains motivated an empirical model which was very successful in simulating the experimental results considered.