Abiomedical Engineering,
bSchool of Mathematics, Statistics and Applied Mathematics,
Abstract
The Holzapfel–Gasser–Ogden (HGO) model for anisotropic hyper- elastic behaviour of collagen fibre reinforced materials was initially developed to describe the elastic properties of arterial tissue, but is now used extensively for modelling a variety of soft biological tissues.
Such materials can be regarded as incompressible, and when the in- compressibility condition is adopted the strain energy Ψ of the HGO model is a function of one isotropic and two anisotropic deformation invariants. A compressible form (HGO-C model) is widely used in fi- nite element simulations whereby the isotropic part of Ψ is decoupled into volumetric and isochoric parts and the anisotropic part of Ψ is expressed in terms of isochoric invariants. Here, by using three simple deformations (pure dilatation, pure shear and uniaxial stretch), we demonstrate that the compressible HGO-C formulation does not cor- rectly model compressible anisotropic material behaviour, because the anisotropic component of the model is insensitive to volumetric defor- mation due to the use of isochoric anisotropic invariants. In order to
Arxiv:2009.08754V1 [Cond-Mat.Soft] 18 Sep 2020
correctly model compressible anisotropic behaviour we present a mod- ified anisotropic (MA) model, whereby the full anisotropic invariants are used, so that a volumetric anisotropic contribution is represented.
The MA model correctly predicts an anisotropic response to hydro- static tensile loading, whereby a sphere deforms into an ellipsoid. It also computes the correct anisotropic stress state for pure shear and uniaxial deformation. To look at more practical applications, we de- veloped a finite element user-defined material subroutine for the sim- ulation of stent deployment in a slightly compressible artery. Signifi- cantly higher stress triaxiality and arterial compliance are computed when the full anisotropic invariants are used (MA model) instead of the isochoric form (HGO-C model).
Keywords Anisotropic, Hyperelastic, Incompressibility, Finite element,
I – Identity Tensor
Ψ – Helmholtz free-energy (strain-energy) function
Ψvol – Volumetric Contribution To The Free Energy
Ψaniso – anisotropic contribution to the free energy Ψiso – isotropic contribution to the isochoric free energy Ψaniso – anisotropic contribution to the isochoric free energy
F – Deformation Gradient
J – determinant of the deformation gradient; local ratio of volume change
I1 – First Invariant Of C
I4,6 – anisotropic invariants describing the deformation of reinforcing fibres
F – Isochoric Portion Of The Deformation Gradient
C – isochoric portion of the right Cauchy–Green deformation tensor
I4,6 – Isochoric Anisotropic Invariants
a0i, i = 4, 6 – unit vector aligned with a reinforcing fibre in the reference
Configuration
ai, i = 4, 6 – updated (deformed) fibre direction (= Fa0i)
Ν – Isotropic Poisson’S Ratio
Bold uppercase symbols represent second order tensors, bold lowercase sym- bols represent vectors and un-bold symbols represent scalars.
Introduction
The anisotropic hyperelastic constitutive model proposed by Holzapfel et al. (2000) (henceforth referred to as the HGO model) is used extensively to model collagen fibre-reinforced biological materials, even more so now that it has been implemented in several commercial and open-source Finite Element (FE) codes for the simulation of soft tissue elasticity.
The constitutive equation builds upon previously published transversely isotropic constitutive models (e.g. Weiss et al. (1996)) and reflects the struc- tural components of a typical biological soft tissue, and hence its strain- energy density consists of two mechanically equivalent terms accounting for the anisotropic contributions of the reinforcing fibre families, in addition to a term representing the isotropic contribution of the ground matrix in which the fibres are embedded. Also, it assumes that the collagen fibres do not support compression, and hence they provide a mechanical contribution only when in tension (this may be taken care of by pre-multiplying each anisotropic term with a Heaviside, or “switching”, function).
For the original incompressible HGO model the strain energy Ψ is ex- pressed as a function of one isochoric isotropic deformation invariant (denoted I1) and two isochoric anisotropic invariants (denoted I4 and I6). A Lagrange multiplier is used to enforce incompressibility (Holzapfel et al., 2000). Once again it should be stressed that the original HGO model is intended only for the simulation of incompressible materials.
A modification of the original HGO model commonly implemented in fi- nite element codes entails the replacement of the Lagrange multiplier penalty term with an isotropic hydrostatic stress term that depends on a user speci- fied bulk modulus. This modification allows for the relaxation of the incom-
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pressibility condition and we therefore refer to this modified formulation as the HGO-C (compressible) model for the remainder of this study. The HGO-C model has been widely used for the finite element simulation of many anisotropic soft tissues. For example, varying degrees of compress- ibility have been reported for cartilage in the literature (e.g. Guilak et al.
(1995); Smith (2001)). It has been modelled as a compressible material using the HGO-C model (e.g. Pe˜na et al. (2007) used a Poisson’s ratio, ν = 0.1 and P´erez del Palomar et al. (2006) used ν = 0.1 and ν = 0.4). To date, material compressibility of arterial tissue has not been firmly established.
Incompressibility was assumed by the authors of the original HGO model and in subsequent studies (e.g. Kiousis et al. (2009)). However many studies model arteries as compressible or slightly compressible (e.g. Cardoso et al.
(2014) ν = 0.33 −0.43 and Iannaccone et al. (2014) ν = 0.475). In addition to arterial tissue the nucleus pulposus of an inter-vertebral disc has been modelled as a compressible anisotropic material using the HGO-C model (e.g. (Maquer et al., 2014) ν = 0.475). Furthermore the HGO-C formulation has been used to simulate growth of anisotropic biological materials, where volume change is an intrinsic part of a bio-mechanical process (e.g. (Huang et al., 2012) ν = 0.3). However, the enforcement of perfect incompressibility may not be readily achieved in numerical models. As an example, the fi- nite element solver Abaqus/Explicit assigns a default Poisson’s ratio of 0.475 to ”incompressible” materials in order to achieve a stable solution (Abaqus, 2010) and in this case the HGO-C model must be used (e.g. Conway et al. (2012); Famaey et al. (2012)). Despite the widespread use of the HGO- C model, its ability to correctly simulate anisotropic compressible material behaviour has not previously been established.
• The first objective of this study is to demonstrate that the HGO-C formulation does not correctly model an anisotropic compressible hy- perelastic material.
Recently, Vergori et al. (2013) showed that under hydrostatic tension, a sphere consisting of a slightly compressible HGO-C material expands into a larger sphere instead of deforming into an ellipsoid. It was suggested that this effectively isotropic response is due to the isochoric anisotropic invariants Ii being used in the switching function instead of the full invariants Ii, i = 4, 6.
However, in the current paper we show that the problem emerges fundamen- tally because there is no dilatational contribution to the anisotropic terms of
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Ψ. In fact, modifying only the “switching criterion” for fibre lengthening is not sufficient to fully redress the problem. • The second objective of the study is to implement a modification of the HGO-C model so that correct anisotropic behaviour of compressible materials is achieved.
This modified anisotropic (MA) model uses the full form of the anisotropic invariants and through a range of case studies we show this leads to the correct computation of stress in contrast to the widely used HGO-C model.
The paper is structured as follows. In Section 2 we demonstrate and high- light the underlying cause of the insensitivity of the anisotropic component of the HGO-C model to volumetric deformation in compressible materials.
We demonstrate that the modification of the model to include the full form of the anisotropic invariants corrects this deficiency. In Section 3 we show how the HGO-C model yields unexpected and unphysical results for pure in- plane shear and likewise in 4 for simple uniaxial stretching, in contrast to the modified model. We devote Section 5 to two Finite Element biomechanics case studies, namely pressure expansion of an artery and stent deployment in an artery, and illustrate the significant differences in computed results for the HGO-C model and the modified model. Finally, we provide some concluding remarks and discussion points in Section 6.
Hgo-C Model For Compressible Materials
The original HGO model is intended for incompressible materials. However a variation of the HGO model whereby a bulk modulus is used instead of a penalty term has been implemented in a number of FE codes. Several authors have used this formulation t model compressible anisotropic materials bu using a relatively low value of bulk modulus. An important objective of this paper is to highlight that this HGO-C formulation does not correctly model compressible anisotropic material behaviour.
The kinematics of deformation are described locally in terms of the defor- mation gradient tensor, denoted F, relative to some reference configuration.
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The right Cauchy–Green tensor is defined by C = FTF, where T indicates the transpose of a second-order tensor. Hyperelastic constitutive models used for rubber-like materials often split the local deformation into volume-changing (volumetric) and volume-preserving (isochoric, or deviatoric) parts. Accordingly the deformation gradient F is
(1)
where J is the determinant of F. The term in the brackets represents the volumetric portion of the deformation gradient and F is its isochoric portion, such that det(F) = 1 at all times.
Suppose that the material consists of an isotropic matrix material within which are embedded two families of fibres characterized by two preferred directions in the reference configuration defined in terms of two unit vectors a0i, i = 4, 6. With C, J and a0i are defined the invariants
(3)
where Ii (i = 1, 4, 6) are the isochoric counterparts of Ii. The HGO model proposed by Holzapfel et al. (2000) for collagen reinforced soft tissues ad- ditively splits the strain energy Ψ into volumetric, isochoric isotropic and
(4)
where Ψiso and Ψaniso are the isochoric isotropic and isochoric anisotropic free-energy contributions, respectively, and C = J−2/3C is the isochoric right Cauchy–Green deformation tensor.
In numerical implementations of the model (Abaqus, 2010; ADINA, 2005; Gasser et al., 2002), the volumetric and isochoric isotropic terms are repre- sented by the slightly compressible neo-Hookean hyperelastic free energy
(5)
where κ0 and µ0 are the bulk and shear moduli, respectively, of the soft isotropic matrix. Of course one may write (5) in terms of the full invariants also, using the results from (3).
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The isochoric anisotropic free-energy term is prescribed as
(6)
where k1 and k2 are positive material constants which can be determined from experiments. For a general hyperelastic material with free energy Ψ the Cauchy stress
(7)
For the Cauchy stress derived from Ψ above, we have the decomposition
(9)
where ai = Fa0i. This slightly compressible implementation is referred to as the HGO-C model henceforth. The original incompressible HGO model by Holzapfel et al. (2000) speci- fied that for arteries the constitutive formulation should be implemented for incompressible materials. In that limit, κ0 →∞, (J −1) →0 while the product of these two quantities becomes an indeterminate Lagrange multi- plier, p, and the volumetric stress assumes the form, σvol = −pI. Indeed the original incompressible HGO model can equally be expressed in terms of the full invariants I4 and I6 (with J →1) (e.g., Holzapfel et al. (2004)).
However, in the case of the HGO-C implementation, if κ0 is not fixed numerically at a large enough value, then slight compressibility is intro- duced into the model.
The Key Point Of This Paper Is That The Isochoric
anisotropic term Ψaniso defined in (6) does not provide a full representation of the anisotropic contributions to the stress tensor for slightly compress- ible materials.
In Section 2.4 we introduce a simple modification of the anisotropic term to account for material compressibility.
Pure Dilatational Deformation
First we consider the case of the HGO-C material subjected to a pure dilata-
C = Λ2I,
J = λ3.
(10)
We expect that an anisotropic material requires an anisotropic stress state to maintain the pure dilatation. However, calculation of the invariants Ii and
(11)
so that while Ii is indeed the square of the fibre stretch and changes with the magnitude of the dilatation, its isochoric counterpart Ii is always unity. Referring to (9), it is clear that the entire anisotropic contribution to the stress (7) disappears (i.e. σaniso ≡0), and the remaining active terms are the isotropic ones. Thus, under pure dilatation, the HGO-C model computes an entirely isotropic state of stress.
Applied Hydrostatic Stress
Now we investigate the reverse question: what is the response of the HGO-C
(12)
where σ > 0 under tension and σ < 0 under pressure? In an anisotropic material, we expect the eigenvalues of C, the squared principal stretches,
2, Λ2
3 say, to be distinct. Hence, if the material is slightly compressible, then a sphere should deform into an ellipsoid (Vergori et al., 2013) and a cube should deform into a hexahedron with non-parallel faces (N´ı Annaidh et al., 2013b).
However, in the HGO-C model the Ψaniso contribution is switched on only when Ii (not Ii) is greater than unity. Vergori et al. (2013) showed that in fact Ii is always less than or equal to one in compression and in expansion under hydrostatic stress, so that the HGO-C response is isotropic, contrary to physical expectations. Then we may ask if removal of the switching function circumvents this problem so that anisotropic response is obtained.
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With the fibres taken to be mechanically equivalent and aligned with a04 = (cos Θ, sin Θ, 0) and a06 = (cos Θ, −sin Θ, 0) in the reference config- uration, we have, by symmetry, I6 = I4 and I6 = I4 and Ψ6 = Ψ4, where the subscripts 4 and 6 on Ψ signify partial differentiation with respect to I4 and I6, respectively. Similarly, in the following the subscript 1 indicates differentiation with respect to I1. For this special case, Vergori et al. (2013) showed that the stretches arising from the application of a hydrostatic stress
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.