Mokarram Hossain

A theory of finite deformation magneto-viscoelasticity

This paper deals with the mathematical modelling of large strain magneto-viscoelastic deformations. Energy dissipation is assumed to occur both due to the mechanical viscoelastic effects as well as the resistance offered by the material to magnetisation. Existence of internal damping mechanisms in the body is considered by decomposing the deformation gradient and the magnetic induction into ‘elastic’ and ‘viscous’ parts. Constitutive laws for material behaviour and evolution equations for the non-equilibrium fields are derived that agree with the laws of thermodynamics. To illustrate the theory the problems of stress relaxation, magnetic field relaxation, time dependent magnetic induction and strain are formulated and solved for a specific form of the constitutive law. The results, that show the effect of several modelling parameters on the deformation and magnetisation process, are illustrated graphically.

Nonlinear magneto-viscoelasticity of transversally isotropic magneto-active polymers

Iron-filled magnetorheological polymers, when cured in the presence of a magnetic field, result in having a transversely isotropic structure with iron particles forming chains along the direction of applied magnetic induction. In this work, we model the magneto-viscoelastic deformation (and magnetization) process of such polymers. Components of the deformation gradient and the applied magnetic induction in the direction of anisotropy are considered to be additional arguments of the energy density function. The existence of internal damping mechanisms is considered by performing a multiplicative decomposition of the deformation gradient and an additive decomposition of the magnetic induction into equilibrium and non-equilibrium parts. Energy density functions and evolution laws of the internal variables are proposed that agree with the laws of thermodynamics. In the end, we present solutions of some standard deformation cases to illustrate the theory. In particular, it is shown that the orientation of resultant magnetic field and principal stress directions change with time owing to viscoelastic evolution.

More hyperelastic models for rubber-like materials: consistent tangent operators and comparative study

Abstract Rubber-like materials can deform largely and nonlinearly upon loading, and they return to the initial configuration when the load is removed. Such rubber elasticity is achieved due to very flexible long-chain molecules and a three-dimensional network structure that is formed via cross-linking or entanglements between molecules. Over the years, to model the mechanical behavior of such randomly oriented microstructures, several phenomenological and micromechanically motivated network models for nearly incompressible hyperelastic polymeric materials have been proposed in the literature. To implement these models for polymeric material (undoubtedly with widespread engineering applications) in the finite element framework for solving a boundary value problem, one would require two important ingredients, i.e., the stress tensor and the consistent fourth-order tangent operator, where the latter is the result of linearization of the former. In our previous work, 14 such material models are reviewed by deriving the accurate stress tensors and tangent operators from a group of phenomenological and micromechanical models at large deformations. The current contribution will supplement some further important models that were not included in the previous work. For comparison of all selected models in reproducing the well-known Treloar data, the analytical expressions for the three homogeneous defomation modes, i.e., uniaxial tension, equibiaxial tension, and pure shear, have been derived and the performances of the models are analyzed.

Eight-chain and full-network models and their modified versions for rubber hyperelasticity: a comparative study

Abstract The eight-chain model, also known as Arruda-Boyce model, is widely used to capture the rate-independent hyperelastic response of rubber-like materials. The parameters of this model are physically based and explained from micromechanics of chain molecules. Despite its excellent performance with only two material parameters to capture bench measurements in uniaxial and pure shear regime, the model is known to be significantly deficient in predicting the equibiaxial data. To ameliorate such drawback, over the years, several modified versions of this successful model have been proposed in the literature. The so-called full-network model is another micromechanically motivated chain model, which has also few modified versions in the literature. For this study, two modified versions of the full-network model have been selected. In this contribution, five modified versions of the Arruda-Boyce model and two modified versions of full-network model are critically compared with the classical eight-chain model for their adequacy in representing equibiaxial data. To do a comparison of all selected models in reproducing the well-known Treloar data, the analytical expressions for the three homogeneous deformation modes, that is, uniaxial tension, equibiaxial tension, and pure shear have been derived and the performances of the selected models are analysed. The comparative study demonstrates that modified Flory-Erman model, Gornet-Desmorat (GD) model, Meissner-Matějka model, and bootstrapped eight-chain model predict well the three deformation modes compare to the classical eight-chain model.

On nonlinear thermo-electro-elasticity

Electro-active polymers (EAPs) for large actuations are nowadays well-known and promising candidates for producing sensors, actuators and generators. In general, polymeric materials are sensitive to differential temperature histories. During experimental characterizations of EAPs under electro-mechanically coupled loads, it is difficult to maintain constant temperature not only because of an external differential temperature history but also because of the changes in internal temperature caused by the application of high electric loads. In this contribution, a thermo-electro-mechanically coupled constitutive framework is proposed based on the total energy approach. Departing from relevant laws of thermodynamics, thermodynamically consistent constitutive equations are formulated. To demonstrate the performance of the proposed thermo-electro-mechanically coupled framework, a frequently used non-homogeneous boundary-value problem, i.e. the extension and inflation of a cylindrical tube, is solved analytically. The results illustrate the influence of various thermo-electro-mechanical couplings.

A novel spectral formulation for transversely isotropic magneto-elasticity

Classical invariants, despite most of them having unclear physical interpretation and not having experimental advantages, have been extensively used in modeling nonlinear magneto-elastic materials. In this paper, a new set of spectral invariants, which have some advantages over classical invariants, is proposed to model the behavior of transversely isotropic nonlinear magneto-elastic bodies. The novel spectral invariant formulation, which is shown to be more general, is used to analytically solve some simple magneto-mechanical boundary value problems. With the aid of the proposed spectral invariants it is possible to study, in a much simpler manner, the effect of different types of deformations on the response of the magneto-elastic material.

On finite strain models for nano-filled glassy polymers

The recently proposed constitutive framework based on logarithmic strain space by Miehe et al. (3) is a successful model for the modelling of amorphous glassy polymers. The modular structure of this model makes it attractive especially for the numerical implementation. In this contribution, the Miehe model will be adapted to model the influence of different types of nano-fillers mixed into bulk amorphous glassy polymers. Here, different types of amorphous glassy polymers with various filler content, orientation of nanofillers and loaded by different strain rates have been investigated experimentally. Then, the Miehe model will be extended towards modelling the nano-particle influence in the amorphous glassy polymer which can be conceptualized by adapting the appropriate material parameters. The proposed modified model will finally be validated with experimental data.