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Generalized Newtonian, Bingham and conformation model equations

Definition

Use SI units and an oriented Euclidean three-space with Cartesian coordinates. Here Cr means that coordinate partial derivatives through total order r exist and are continuous. Let I⊆R be a nonempty open interval containing 0, let B⊆R3 be a nonempty bounded open reference body with C1 boundary, and let U be an open neighborhood of B‾. A smooth motion is a map χ∈C2(I×U;R3) such that each χt(a):=χ(t,a) is an orientation-preserving C2 diffeomorphism onto its image; when labels are initially the current positions, χ0(a)=a. Set Ωt=χt(B). For x∈χt(U) its inverse label map is A(t,x)=χt−1(x), and its Eulerian velocity is u(t,x)=∂tχ(t,A(t,x)). Position and material-label coordinates have units m, time has units s, and velocity has units m s−1. The velocity gradient is L=∇u, the rate-of-strain tensor is D=(L+LT)/2, the spin is W=(L−LT)/2, and the dilatation is θ=tr⁡D=tr⁡L; all have units s−1. The material derivative is Dt=∂t+u⋅∇, acting componentwise on tensor fields, with units s−1 on dimensionless fields. Matrix contraction is S:T=tr⁡(STT), with Frobenius norm ∣S∣=(S:S)1/2. These definitions are the mathematical motion and kinematics used below.

Let M3(R) denote the real 3×3 matrices and I3 the identity matrix. Write Sym0(3)={D∈M3(R):DT=D,tr⁡D=0}. The generalized Newtonian branch is incompressible, so θ=0 and D∈Sym0(3). Define the shear-rate scalar γ˙=(2D:D)1/2, with units s−1, and let η(γ˙) be a finite nonnegative viscosity with units Pa s. The deviatoric stress is τ=2η(γ˙)D, in Pa; no pressure term is included.

For a>0 and r∈R, use the positive-base real power ar:=exp⁡(rlog⁡nata), where log⁡nat denotes the natural logarithm. The formulas apply this power to positive numerical values in the fixed SI units, with the resulting unit exponents carried by the listed parameter units. This is the convention in the viscosity formulas below; the unregularized form is evaluated only when γ˙>0. The integral logarithm log⁡ used in the conformation branch is defined separately there.

Two named viscosity choices are the Carreau form

ηC(γ˙)=η∞+(η0−η∞)(1+(λγ˙)2)(n−1)/2,

with η0≥η∞≥0 in Pa s, λ≥0 in s, and dimensionless n>0, and the regularized power form

ηR(γ˙)=m(ε2+γ˙2)(n−1)/2,

with m>0 in Pa sn, ε>0 in s−1, and dimensionless n>0. For comparison, the unregularized power form ηU=mγ˙ n−1 is defined only for γ˙>0; its stress is extended by τ=0 at D=0. When 0<n<1, this viscosity diverges as γ˙↓0, although the extended stress may remain continuous.

For the Bingham branch use the Frobenius norm just defined, μp≥0 in Pa s, and yield parameter τy≥0 in Pa. Its set-valued deviatoric stress graph on Sym0(3) is

B(D)={{2μpD+τyD/∣D∣},D≠0,{S∈Sym0(3):∣S∣≤τy},D=0.

The value at rest is therefore a whole stress ball when τy>0. The chosen Frobenius normalization fixes the numerical convention for τy; a source using a differently normalized second invariant requires a corresponding parameter conversion.

For the conformation branch, set Sym(3)={M∈M3(R):M=MT} and Sym+(3)={M∈Sym(3):vTMv>0 for every v∈R3∖{0}}. On the swept open set Ω={(t,x)∈I×R3:x∈χt(U)} from the smooth-motion definition, let the dimensionless conformation field be C∈C1(Ω;Sym(3)). Thus C is a C1 matrix-valued field, and DtC=∂tC+u⋅∇C is defined componentwise. The ambient state space for the evolution equation is Sym(3); the stored-energy function below is defined only on the admissible subset Sym+(3), and this definition does not assume that a solution remains in that subset along a trajectory.

For each C∈Sym+(3), the finite-dimensional real spectral theorem supplies an orthonormal eigenbasis v1,v2,v3 with Cvi=civi. Positive definiteness gives ci=viTCvi>0 for each unit eigenvector vi, and determinant multiplicativity then gives det⁡C=c1c2c3>0. Define log⁡:(0,∞)→R by log⁡r=∫1rds/s. Let G>0 be a modulus in Pa, λ>0 a relaxation time in s, and ηs≥0 a solvent viscosity in Pa s. On an incompressible motion, meaning div⁡u=tr⁡L=0, adopt the conformation equation and stress and storage definitions

DtC−LC−CLT=−(C−I3)/λ,τp=G(C−I3),τs=2ηsD,w(C)=G2(tr⁡C−log⁡det⁡C−3).

Here both sides of the conformation equation have units s−1; τp,τs are polymer and solvent stresses in Pa, and w is a stored-energy density in J m−3. The equation is defined for symmetric matrix fields, while w is evaluated only where C is positive definite. These are mathematical constitutive definitions and adopted model equations. They assert neither empirical validity for a particular material nor existence of a solution to a fluid partial differential equation.

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