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Template:Continuum mechanics In continuum mechanics, an Arruda–Boyce model[1] is a hyperelastic constitutive model used to describe the mechanical behavior of rubber and other polymeric substances. This model is based on the statistical mechanics of a material with a cubic representative volume element containing eight chains along the diagonal directions. The material is assumed to be incompressible.

The strain energy density function for the incompressible Arruda–Boyce model is given by[2]

W=NkBθn[βλchainnln(sinhββ)]

where N is the number of chain segments, kB is the Boltzmann constant, θ is the temperature in Kelvin, n is the number of chains in the network of a cross-linked polymer,

λchain=I13;β=1(λchainn)

where I1 is the first invariant of the left Cauchy–Green deformation tensor, and 1(x) is the inverse Langevin function which can approximated by

1(x)={1.31tan(1.59x)+0.91xfor|x|<0.8411sgn(x)xfor0.841|x|<1

For small deformations the Arruda–Boyce model reduces to the Gaussian network based neo-Hookean solid model. It can be shown[3] that the Gent model is a simple and accurate approximation of the Arruda–Boyce model.

Alternative expressions for the Arruda–Boyce model

An alternative form of the Arruda–Boyce model, using the first five terms of the inverse Langevin function, is[4]

W=C1[12(I13)+120N(I129)+111050N2(I1327)+197000N3(I1481)+519673750N4(I15243)]

where C1 is a material constant. The quantity N can also be interpreted as a measure of the limiting network stretch.

If λm is the stretch at which the polymer chain network becomes locked, we can express the Arruda–Boyce strain energy density as

W=C1[12(I13)+120λm2(I129)+111050λm4(I1327)+197000λm6(I1481)+519673750λm8(I15243)]

We may alternatively express the Arruda–Boyce model in the form

W=C1i=15αiβi1(I1i3i)

where β:=1N=1λm2 and α1:=12;α2:=120;α3:=111050;α4:=197000;α5:=519673750.

If the rubber is compressible, a dependence on J=det(F) can be introduced into the strain energy density; F being the deformation gradient. Several possibilities exist, among which the Kaliske–Rothert[5] extension has been found to be reasonably accurate. With that extension, the Arruda-Boyce strain energy density function can be expressed as

W=D1(J212lnJ)+C1i=15αiβi1(I1i3i)

where D1 is a material constant and I1=I1J2/3 . For consistency with linear elasticity, we must have D1=κ2 where κ is the bulk modulus.

Consistency condition

For the incompressible Arruda–Boyce model to be consistent with linear elasticity, with μ as the shear modulus of the material, the following condition has to be satisfied:

WI1|I1=3=μ2.

From the Arruda–Boyce strain energy density function, we have,

WI1=C1i=15iαiβi1I1i1.

Therefore, at I1=3,

μ=2C1i=15iαiβi1I1i1.

Substituting in the values of αi leads to the consistency condition

μ=C1(1+35λm2+99175λm4+513875λm6+4203967375λm8).

Stress-deformation relations

The Cauchy stress for the incompressible Arruda–Boyce model is given by

σ=p1+2WI1B=p1+2C1[i=15iαiβi1I1i1]B

Uniaxial extension

Stress-strain curves under uniaxial extension for Arruda–Boyce model compared with various hyperelastic material models.

For uniaxial extension in the n1-direction, the principal stretches are λ1=λ,λ2=λ3. From incompressibility λ1λ2λ3=1. Hence λ22=λ32=1/λ. Therefore,

I1=λ12+λ22+λ32=λ2+2λ.

The left Cauchy–Green deformation tensor can then be expressed as

B=λ2n1n1+1λ(n2n2+n3n3).

If the directions of the principal stretches are oriented with the coordinate basis vectors, we have

σ11=p+2C1λ2[i=15iαiβi1I1i1]σ22=p+2C1λ[i=15iαiβi1I1i1]=σ33.

If σ22=σ33=0, we have

p=2C1λ[i=15iαiβi1I1i1].

Therefore,

σ11=2C1(λ21λ)[i=15iαiβi1I1i1].

The engineering strain is λ1. The engineering stress is

T11=σ11/λ=2C1(λ1λ2)[i=15iαiβi1I1i1].

Equibiaxial extension

For equibiaxial extension in the n1 and n2 directions, the principal stretches are λ1=λ2=λ. From incompressibility λ1λ2λ3=1. Hence λ3=1/λ2. Therefore,

I1=λ12+λ22+λ32=2λ2+1λ4.

The left Cauchy–Green deformation tensor can then be expressed as

B=λ2n1n1+λ2n2n2+1λ4n3n3.

If the directions of the principal stretches are oriented with the coordinate basis vectors, we have

σ11=2C1(λ21λ4)[i=15iαiβi1I1i1]=σ22.

The engineering strain is λ1. The engineering stress is

T11=σ11λ=2C1(λ1λ5)[i=15iαiβi1I1i1]=T22.

Planar extension

Planar extension tests are carried out on thin specimens which are constrained from deforming in one direction. For planar extension in the n1 directions with the n3 direction constrained, the principal stretches are λ1=λ,λ3=1. From incompressibility λ1λ2λ3=1. Hence λ2=1/λ. Therefore,

I1=λ12+λ22+λ32=λ2+1λ2+1.

The left Cauchy–Green deformation tensor can then be expressed as

B=λ2n1n1+1λ2n2n2+n3n3.

If the directions of the principal stretches are oriented with the coordinate basis vectors, we have

σ11=2C1(λ21λ2)[i=15iαiβi1I1i1];σ22=0;σ33=2C1(11λ2)[i=15iαiβi1I1i1].

The engineering strain is λ1. The engineering stress is

T11=σ11λ=2C1(λ1λ3)[i=15iαiβi1I1i1].

Simple shear

The deformation gradient for a simple shear deformation has the form[6]

F=1+γe1e2

where e1,e2 are reference orthonormal basis vectors in the plane of deformation and the shear deformation is given by

γ=λ1λ;λ1=λ;λ2=1λ;λ3=1

In matrix form, the deformation gradient and the left Cauchy–Green deformation tensor may then be expressed as

F=[1γ0010001];B=FFT=[1+γ2γ0γ10001]

Therefore,

I1=tr(B)=3+γ2

and the Cauchy stress is given by

σ=p1+2C1[i=15iαiβi1(3+γ2)i1]B

Statistical mechanics of polymer deformation

Mining Engineer (Excluding Oil ) Truman from Alma, loves to spend time knotting, largest property developers in singapore developers in singapore and stamp collecting. Recently had a family visit to Urnes Stave Church. The Arruda–Boyce model is based on the statistical mechanics of polymer chains. In this approach, each macromolecule is described as a chain of N segments, each of length l. If we assume that the initial configuration of a chain can be described by a random walk, then the initial chain length is

r0=lN

If we assume that one end of the chain is at the origin, then the probability that a block of size dx1dx2dx3 around the origin will contain the other end of the chain, (x1,x2,x3), assuming a Gaussian probability density function, is

p(x1,x2,x3)=b3π3/2exp[b2(x12+x22+x32)];b:=32Nl2

The configurational entropy of a single chain from Boltzmann statistical mechanics is

s=ckBb2r2

where c is a constant. The total entropy in a network of n chains is therefore

ΔS=12nkB(λ12+λ22+λ323)=12nkB(I13)

where an affine deformation has been assumed. Therefore the strain energy of the deformed network is

W=θdS=12nkBθ(I13)

where θ is the temperature.

Notes and references

  1. Arruda, E. M. and Boyce, M. C., 1993, A three-dimensional model for the large stretch behavior of rubber elastic materials,, J. Mech. Phys. Solids, 41(2), pp. 389–412.
  2. Bergstrom, J. S. and Boyce, M. C., 2001, Deformation of Elastomeric Networks: Relation between Molecular Level Deformation and Classical Statistical Mechanics Models of Rubber Elasticity, Macromolecules, 34 (3), pp 614–626, 21 year-old Glazier James Grippo from Edam, enjoys hang gliding, industrial property developers in singapore developers in singapore and camping. Finds the entire world an motivating place we have spent 4 months at Alejandro de Humboldt National Park..
  3. Horgan, C.O. and Saccomandi, G., 2002, A molecular-statistical basis for the Gent constitutive model of rubber elasticity, Journal of Elasticity, 68(1), pp. 167–176.
  4. Hiermaier, S. J., 2008, Structures under Crash and Impact, Springer.
  5. Kaliske, M. and Rothert, H., 1997, On the finite element implementation of rubber-like materials at finite strains, Engineering Computations, 14(2), pp. 216–232.
  6. Ogden, R. W., 1984, Non-linear elastic deformations, Dover.

See also