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ARUP; ISBN: 978-0-9562121-5-3 - CMBBE 2012 - Cardiff University

ARUP; ISBN: 978-0-9562121-5-3 - CMBBE 2012 - Cardiff University

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one cements as well as its behaviour in solid state. The parameters of the material<br />

model have been fitted to one specific acrylic bone cement. Furthermore, the model has<br />

been implemented into a commercial finite element code. The capability of our material<br />

model will be demonstrated by the help of finite element simulations using a parametric<br />

model of a vertebral body of the lumbar spine.<br />

3. MATERIAL MODEL FOR ACRYLIC BONE CEMENTS<br />

The material model presented in [1] is based on the standard concepts of nonlinear<br />

continuum mechanics, e.g. the application of strain and stress measures at large<br />

deformations and the evaluation of the laws of thermodynamics to obtain a<br />

thermodynamically consistent material behaviour. The material response is assumed to<br />

be nearly incompressible combined with viscoelastic behaviour of the isochoric part. A<br />

formulation of a chain of Maxwell-elements connected in parallel is employed to define<br />

the viscoelastic behaviour. Furthermore, a degree of cure is introduced to describe the<br />

progress of the chemical process of polymerization. This variable is treated as an<br />

internal variable within the material model. Finally, the consideration of the temperature<br />

θ within different material functions as well as the evaluation of the transient heat<br />

equation leads to a fully thermochemical-mechanically coupled material model.<br />

The underlying kinematics is described by the deformation gradient . To separate<br />

different sources of deformation, a multiplicative decomposition of the deformation<br />

gradient is applied. Firstly, thermo-chemical volume changes due to heat expansion and<br />

chemical shrinkage are separated from pure mechanical deformations according to eq.<br />

(1). Therein the thermo-chemical volume changes are assumed to be isotropic and<br />

therefore can be described by a scalar material function .<br />

= ∙ <br />

<br />

= = , (1)<br />

Next, the mechanical deformation gradient is split into a pure volumetric part ,<br />

which depends on the determinant of the mechanical deformation gradient, and a<br />

remaining volume preserving (isochoric) deformation gradient (cf. eq. (2)). The<br />

latter part is employed for the formulation of the viscoelastic material behaviour.<br />

= ∙ <br />

<br />

= <br />

= det = 1/ In order to fulfil the laws of thermodynamics and to ensure a thermodynamically<br />

consistent material behaviour, a free energy function has been formulated. It is<br />

additively decomposed into three parts. The first part represents a pure elastic<br />

material behaviour due to volumetric changes. Secondly, a volume preserving,<br />

viscoelastic part = ∑ , is modelled, which consist of a sum of free energy<br />

functions for = 1 … Maxwell-elements. The last part is a thermo-chemical part describing thermally stored amounts as well as initially stored energy which is getting<br />

released due to the exothermal chemical reaction.<br />

An evaluation of the chosen ansatz for the free energy function within the laws of<br />

thermodynamics leads to a coupled system of equations which describes the thermomechanically<br />

coupled material behaviour. Among others, it consists of an equation for<br />

the 2 nd Piola-Kirchhoff stress (eq. (3)) including a bulk modulus as well as stiffness<br />

parameters and relaxation times = /2 for each of the Maxwell-Elements.<br />

(2)

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