Hyperelastic material

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File:Hyperelastic.svg
Stress–strain curves for various hyperelastic material models.

A hyperelastic or Green elastic material[1] is a type of constitutive model for ideally elastic material for which the stress–strain relationship derives from a strain energy density function. The hyperelastic material is a special case of a Cauchy elastic material. For many materials, linear elastic models do not accurately describe the observed material behaviour. The most common example of this kind of material is rubber, whose stress-strain relationship can be defined as non-linearly elastic, isotropic and incompressible. Hyperelasticity provides a means of modeling the stress–strain behavior of such materials.[2] The behavior of unfilled, vulcanized elastomers often conforms closely to the hyperelastic ideal. Filled elastomers and biological tissues[3][4] are also often modeled via the hyperelastic idealization. In addition to being used to model physical materials, hyperelastic materials are also used as fictitious media, e.g. in the third medium contact method. Ronald Rivlin and Melvin Mooney developed the first hyperelastic models, the Neo-Hookean and Mooney–Rivlin solids. Many other hyperelastic models have since been developed. Other widely used hyperelastic material models include the Ogden model and the Arruda–Boyce model.

Hyperelastic material models

Saint Venant–Kirchhoff model

The simplest hyperelastic material model is the Saint Venant–Kirchhoff model which is just an extension of the geometrically linear elastic material model to the geometrically nonlinear regime. This model has the general form and the isotropic form respectively S=C:ES=λtr(E)I+2μE. where : is tensor contraction, S is the second Piola–Kirchhoff stress, C:3×33×3 is a fourth order stiffness tensor and E is the Lagrangian Green strain given by E=12[(Xu)T+Xu+(Xu)TXu] λ and μ are the Lamé constants, and I is the second order unit tensor. The strain-energy density function for the Saint Venant–Kirchhoff model is W(E)=λ2[tr(E)]2+μtr(E2) and the second Piola–Kirchhoff stress can be derived from the relation S=WE.

Classification of hyperelastic material models

Hyperelastic material models can be classified as:

  1. phenomenological descriptions of observed behavior
  2. mechanistic models deriving from arguments about the underlying structure of the material
  3. hybrids of phenomenological and mechanistic models

Generally, a hyperelastic model should satisfy the Drucker stability criterion. Some hyperelastic models satisfy the Valanis-Landel hypothesis which states that the strain energy function can be separated into the sum of separate functions of the principal stretches (λ1,λ2,λ3): W=f(λ1)+f(λ2)+f(λ3).

Stress–strain relations

Compressible hyperelastic materials

First Piola–Kirchhoff stress

If W(F) is the strain energy density function, the 1st Piola–Kirchhoff stress tensor can be calculated for a hyperelastic material as P=WForPiK=WFiK. where F is the deformation gradient. In terms of the Lagrangian Green strain (E) P=FWEorPiK=FiLWELK. In terms of the right Cauchy–Green deformation tensor (C) P=2FWCorPiK=2FiLWCLK.

Second Piola–Kirchhoff stress

If S is the second Piola–Kirchhoff stress tensor then S=F1WForSIJ=FIk1WFkJ. In terms of the Lagrangian Green strain S=WEorSIJ=WEIJ. In terms of the right Cauchy–Green deformation tensor S=2WCorSIJ=2WCIJ. The above relation is also known as the Doyle-Ericksen formula in the material configuration.

Cauchy stress

Similarly, the Cauchy stress is given by σ=1JWFFT;J:=detForσij=1JWFiKFjK. In terms of the Lagrangian Green strain σ=1JFWEFTorσij=1JFiKWEKLFjL. In terms of the right Cauchy–Green deformation tensor σ=2JFWCFTorσij=2JFiKWCKLFjL. The above expressions are valid even for anisotropic media (in which case, the potential function is understood to depend implicitly on reference directional quantities such as initial fiber orientations). In the special case of isotropy, the Cauchy stress can be expressed in terms of the left Cauchy-Green deformation tensor as follows:[7] σ=2JWBBorσij=2JBikWBkj.

Incompressible hyperelastic materials

For an incompressible material J:=detF=1. The incompressibility constraint is therefore J1=0. To ensure incompressibility of a hyperelastic material, the strain-energy function can be written in form: W=W(F)p(J1) where the hydrostatic pressure p functions as a Lagrangian multiplier to enforce the incompressibility constraint. The 1st Piola–Kirchhoff stress now becomes P=pJFT+WF=pFT+FWE=pFT+2FWC. This stress tensor can subsequently be converted into any of the other conventional stress tensors, such as the Cauchy stress tensor which is given by σ=PFT=p1+WFFT=p1+FWEFT=p1+2FWCFT.

Expressions for the Cauchy stress

Compressible isotropic hyperelastic materials

For isotropic hyperelastic materials, the Cauchy stress can be expressed in terms of the invariants of the left Cauchy–Green deformation tensor (or right Cauchy–Green deformation tensor). If the strain energy density function is W(F)=W^(I1,I2,I3)=W¯(I¯1,I¯2,J)=W~(λ1,λ2,λ3), then σ=2I3[(W^I1+I1W^I2)BW^I2BB]+2I3W^I31=2J[1J2/3(W¯I¯1+I¯1W¯I¯2)B1J4/3W¯I¯2BB]+[W¯J23J(I¯1W¯I¯1+2I¯2W¯I¯2)]1=2J[(W¯I¯1+I¯1W¯I¯2)B¯W¯I¯2B¯B¯]+[W¯J23J(I¯1W¯I¯1+2I¯2W¯I¯2)]1=λ1λ1λ2λ3W~λ1n1n1+λ2λ1λ2λ3W~λ2n2n2+λ3λ1λ2λ3W~λ3n3n3 (See the page on the left Cauchy–Green deformation tensor for the definitions of these symbols).

Proof 1

The second Piola–Kirchhoff stress tensor for a hyperelastic material is given by S=2WC where C=FTF is the right Cauchy–Green deformation tensor and F is the deformation gradient. The Cauchy stress is given by σ=1JFSFT=2JFWCFT where J=detF. Let I1,I2,I3 be the three principal invariants of C. Then WC=WI1I1C+WI2I2C+WI3I3C. The derivatives of the invariants of the symmetric tensor C are I1C=1;I2C=I11C;I3C=det(C)C1 Therefore, we can write WC=WI11+WI2(I11FTF)+WI3I3F1FT. Plugging into the expression for the Cauchy stress gives σ=2J[WI1FFT+WI2(I1FFTFFTFFT)+WI3I31] Using the left Cauchy–Green deformation tensor B=FFT and noting that I3=J2, we can write σ=2I3[(WI1+I1WI2)BWI2BB]+2I3WI31. For an incompressible material I3=1 and hence W=W(I1,I2).Then WC=WI1I1C+WI2I2C=WI11+WI2(I11FTF) Therefore, the Cauchy stress is given by σ=2[(WI1+I1WI2)BWI2BB]p1. where p is an undetermined pressure which acts as a Lagrange multiplier to enforce the incompressibility constraint. If, in addition, I1=I2, we have W=W(I1) and hence WC=WI1I1C=WI11 In that case the Cauchy stress can be expressed as σ=2WI1Bp1.

Proof 2

The isochoric deformation gradient is defined as F¯:=J1/3F, resulting in the isochoric deformation gradient having a determinant of 1, in other words it is volume stretch free. Using this one can subsequently define the isochoric left Cauchy–Green deformation tensor B¯:=F¯F¯T=J2/3B. The invariants of B¯ are I¯1=tr(B¯)=J2/3tr(B)=J2/3I1I¯2=12(tr(B¯)2tr(B¯2))=12((J2/3tr(B))2tr(J4/3B2))=J4/3I2I¯3=det(B¯)=J6/3det(B)=J2I3=J2J2=1 The set of invariants which are used to define the distortional behavior are the first two invariants of the isochoric left Cauchy–Green deformation tensor tensor, (which are identical to the ones for the right Cauchy Green stretch tensor), and add J into the fray to describe the volumetric behaviour. To express the Cauchy stress in terms of the invariants I¯1,I¯2,J recall that I¯1=J2/3I1=I31/3I1;I¯2=J4/3I2=I32/3I2;J=I31/2. The chain rule of differentiation gives us WI1=WI¯1I¯1I1+WI¯2I¯2I1+WJJI1=I31/3WI¯1=J2/3WI¯1WI2=WI¯1I¯1I2+WI¯2I¯2I2+WJJI2=I32/3WI¯2=J4/3WI¯2WI3=WI¯1I¯1I3+WI¯2I¯2I3+WJJI3=13I34/3I1WI¯123I35/3I2WI¯2+12I31/2WJ=13J8/3J2/3I¯1WI¯123J10/3J4/3I¯2WI¯2+12J1WJ=13J2(I¯1WI¯1+2I¯2WI¯2)+12J1WJ Recall that the Cauchy stress is given by σ=2I3[(WI1+I1WI2)BWI2BB]+2I3WI31. In terms of the invariants I¯1,I¯2,J we have σ=2J[(WI1+J2/3I¯1WI2)BWI2BB]+2JWI31. Plugging in the expressions for the derivatives of W in terms of I¯1,I¯2,J, we have σ=2J[(J2/3WI¯1+J2/3I¯1WI¯2)BJ4/3WI¯2BB]+2J[13J2(I¯1WI¯1+2I¯2WI¯2)+12J1WJ]1 or, σ=2J[1J2/3(WI¯1+I¯1WI¯2)B1J4/3WI¯2BB]+[WJ23J(I¯1WI¯1+2I¯2WI¯2)]1 In terms of the deviatoric part of B, we can write σ=2J[(WI¯1+I¯1WI¯2)B¯WI¯2B¯B¯]+[WJ23J(I¯1WI¯1+2I¯2WI¯2)]1 For an incompressible material J=1 and hence W=W(I¯1,I¯2).Then the Cauchy stress is given by σ=2[(WI¯1+I1WI¯2)B¯WI¯2B¯B¯]p1. where p is an undetermined pressure-like Lagrange multiplier term. In addition, if I¯1=I¯2, we have W=W(I¯1) and hence the Cauchy stress can be expressed as σ=2WI¯1B¯p1.

Proof 3

To express the Cauchy stress in terms of the stretches λ1,λ2,λ3 recall that λiC=12λiRT(nini)R;i=1,2,3. The chain rule gives WC=Wλ1λ1C+Wλ2λ2C+Wλ3λ3C=RT[12λ1Wλ1n1n1+12λ2Wλ2n2n2+12λ3Wλ3n3n3]R The Cauchy stress is given by σ=2JFWCFT=2J(VR)WC(RTV) Plugging in the expression for the derivative of W leads to σ=2JV[12λ1Wλ1n1n1+12λ2Wλ2n2n2+12λ3Wλ3n3n3]V Using the spectral decomposition of V we have V(nini)V=λi2nini;i=1,2,3. Also note that J=det(F)=det(V)det(R)=det(V)=λ1λ2λ3. Therefore, the expression for the Cauchy stress can be written as σ=1λ1λ2λ3[λ1Wλ1n1n1+λ2Wλ2n2n2+λ3Wλ3n3n3] For an incompressible material λ1λ2λ3=1 and hence W=W(λ1,λ2). Following Ogden[1] p. 485, we may write σ=λ1Wλ1n1n1+λ2Wλ2n2n2+λ3Wλ3n3n3p1 Some care is required at this stage because, when an eigenvalue is repeated, it is in general only Gateaux differentiable, but not Fréchet differentiable.[8][9] A rigorous tensor derivative can only be found by solving another eigenvalue problem. If we express the stress in terms of differences between components, σ11σ33=λ1Wλ1λ3Wλ3;σ22σ33=λ2Wλ2λ3Wλ3 If in addition to incompressibility we have λ1=λ2 then a possible solution to the problem requires σ11=σ22 and we can write the stress differences as σ11σ33=σ22σ33=λ1Wλ1λ3Wλ3

Incompressible isotropic hyperelastic materials

For incompressible isotropic hyperelastic materials, the strain energy density function is W(F)=W^(I1,I2). The Cauchy stress is then given by σ=p1+2[(W^I1+I1W^I2)BW^I2BB]=p1+2[(WI¯1+I1WI¯2)B¯WI¯2B¯B¯]=p1+λ1Wλ1n1n1+λ2Wλ2n2n2+λ3Wλ3n3n3 where p is an undetermined pressure. In terms of stress differences σ11σ33=λ1Wλ1λ3Wλ3;σ22σ33=λ2Wλ2λ3Wλ3 If in addition I1=I2, then σ=2WI1Bp1. If λ1=λ2, then σ11σ33=σ22σ33=λ1Wλ1λ3Wλ3

Consistency with linear elasticity

Consistency with linear elasticity is often used to determine some of the parameters of hyperelastic material models. These consistency conditions can be found by comparing Hooke's law with linearized hyperelasticity at small strains.

Consistency conditions for isotropic hyperelastic models

For isotropic hyperelastic materials to be consistent with isotropic linear elasticity, the stress–strain relation should have the following form in the infinitesimal strain limit: σ=λtr(ε)1+2με where λ,μ are the Lamé constants. The strain energy density function that corresponds to the above relation is[1] W=12λ[tr(ε)]2+μtr(ε2) For an incompressible material tr(ε)=0 and we have W=μtr(ε2) For any strain energy density function W(λ1,λ2,λ3) to reduce to the above forms for small strains the following conditions have to be met[1] W(1,1,1)=0;Wλi(1,1,1)=02Wλiλj(1,1,1)=λ+2μδij If the material is incompressible, then the above conditions may be expressed in the following form. W(1,1,1)=0Wλi(1,1,1)=Wλj(1,1,1);2Wλi2(1,1,1)=2Wλj2(1,1,1)2Wλiλj(1,1,1)=independentofi,ji2Wλi2(1,1,1)2Wλiλj(1,1,1)+Wλi(1,1,1)=2μ(ij) These conditions can be used to find relations between the parameters of a given hyperelastic model and shear and bulk moduli.

Consistency conditions for incompressible I1 based rubber materials

Many elastomers are modeled adequately by a strain energy density function that depends only on I1. For such materials we have W=W(I1). The consistency conditions for incompressible materials for I1=3,λi=λj=1 may then be expressed as W(I1)|I1=3=0andWI1|I1=3=μ2. The second consistency condition above can be derived by noting that Wλi=WI1I1λi=2λiWI1and2Wλiλj=2δijWI1+4λiλj2WI12. These relations can then be substituted into the consistency condition for isotropic incompressible hyperelastic materials.

References

  1. 1.0 1.1 1.2 1.3 1.4 R.W. Ogden, 1984, Non-Linear Elastic Deformations, ISBN 0-486-69648-0, Dover.
  2. Muhr, A. H. (2005). "Modeling the stress–strain behavior of rubber". Rubber Chemistry and Technology. 78 (3): 391–425. doi:10.5254/1.3547890.
  3. Gao, H; Ma, X; Qi, N; Berry, C; Griffith, BE; Luo, X (2014). "A finite strain nonlinear human mitral valve model with fluid-structure interaction". Int J Numer Methods Biomed Eng. 30 (12): 1597–613. doi:10.1002/cnm.2691. PMC 4278556. PMID 25319496.
  4. Jia, F; Ben Amar, M; Billoud, B; Charrier, B (2017). "Morphoelasticity in the development of brown alga Ectocarpus siliculosus: from cell rounding to branching". J R Soc Interface. 14 (127): 20160596. doi:10.1098/rsif.2016.0596. PMC 5332559. PMID 28228537.
  5. Arruda, E.M.; Boyce, M.C. (1993). "A three-dimensional model for the large stretch behavior of rubber elastic materials" (PDF). J. Mech. Phys. Solids. 41: 389–412. doi:10.1016/0022-5096(93)90013-6. S2CID 136924401.
  6. Buche, M.R.; Silberstein, M.N. (2020). "Statistical mechanical constitutive theory of polymer networks: The inextricable links between distribution, behavior, and ensemble". Phys. Rev. E. 102 (1): 012501. arXiv:2004.07874. Bibcode:2020PhRvE.102a2501B. doi:10.1103/PhysRevE.102.012501. PMID 32794915. S2CID 215814600.
  7. Y. Basar, 2000, Nonlinear continuum mechanics of solids, Springer, p. 157.
  8. Fox & Kapoor, Rates of change of eigenvalues and eigenvectors, AIAA Journal, 6 (12) 2426–2429 (1968)
  9. Friswell MI. The derivatives of repeated eigenvalues and their associated eigenvectors. Journal of Vibration and Acoustics (ASME) 1996; 118:390–397.

See also