Viscoelastic Material

Constitutive Laws

This MPM material has separate constitutive laws for deviatoric stress and pressure.

Deviatoric Constitutive Law

The deviatoric constitutive law is always a small-strain, linear viscoelastic material with time-dependent shear modulus, G(t), which is given by a sum of n exponentials:

      [math]\displaystyle{ G(t) = G_0 + \sum_{i=1}^n G_i e^{-t/\tau_i} }[/math]

Here G₀ is the long-time shear modulus and the short-time shear modulus is the sum:

      [math]\displaystyle{ G(0) = \sum_{i=0}^n G_i }[/math]

The updates for components of the deviatoric stress become

      [math]\displaystyle{ ds_{ij} = 2\left( G(0) de_{ij} - \sum_{k=1}^n G_k d\alpha_{ij,k} \right) }[/math]

where α_ij,k are a series of internal variables that are tracked in history variables on each particle.

Pressure Constitutive Law

The pressure constitutive law has two options. The first in to use a small strain linear elastic law with pressure increment of

      [math]\displaystyle{ dP = -K(d\varepsilon_{xx} + d\varepsilon_{yy} + d\varepsilon_{zz} - 3d\varepsilon_{res}) }[/math]

where K is the time-independent bulk modulus and other terms are applied or residual strain increments. To use this law, which is the default, set pressureLaw to 0 and enter the bulk modulus K.

The second option is to use then Mie-Grüneisen equation of state (MGEOS). To use this law, set pressureLaw to 1 and enter the MGEOS properties.

Note that this material always models bulk modulus as a time-independent property (although possible nonlinear elastic). You can model isotropic materials that have a time-dependent bulk modulus by treating them as a special case of a transversely isotropic material.

Plane Stress Analysis

This material can be used in plane stress analysis, but only if it uses the linear pressure law (pressureLaw=0) and it does not add artificial viscosity. Support for plane stress in other conditions may be provided soon.

Effective Time Implementation

The above constitutive law assumes G(t) depends only on time, but in real materials, it will depend strongly on temperature. When modeling diffusion with solvent concentration, it may depend on solvent concentration as well. These dependencies are modeling by assuming the material obeys time-temperature or time-solvent superposition whereby G(t) is given by:

      [math]\displaystyle{ G(t) = G_0 + \sum_{i=1}^n G_i e^{-t/(a\tau_i)} }[/math]

where a is a shift factor. In other words, the coefficient of G(t) remain constant, but the relaxation times shift by a factor a. We are lead to define relaxation using a reduced time, which is effective time at some reference condition, as

      [math]\displaystyle{ G(t_r) = G_0 + \sum_{i=1}^n G_i e^{-t/\tau_i} \quad{\rm and}\quad G(t) = G(t_r/a) }[/math]

The above constitutive law can then be extended to variable environment by converting convolution integrals to integrals of effective time defined by

      [math]\displaystyle{ t_r = \int_0^t \frac{dt}{a} \quad{\rm and}\quad \frac{dt_r}{dt} = \frac{1}{a} }[/math]

To to implement this modeling, the material methods need input for a as a function of environment.

Variable Temperature Environments

For temperature variations, a becomes a_T or the thermal shift factor. In polymer materials, this shift factor is approximated by the WLF equation:

      [math]\displaystyle{ \log \frac{\tau(T)}{\tau(T_{ref})} = \log a_T = - \frac{C_1(T-T_{ref})}{T-T_{ref}+C_2} }[/math]

This shift factor implemented in simulations by entering Tref, C1, and C2. In polymer materials, if T_ref=T_g, or the glass transition temperature, C₁=17.44 and C₂=51.6 are average values of a range of polymers (the value for one specific polymer my vary significantly). If T_ref differs from T_g, it can be used in a shifted WLF equation using C₃ and C₄ defined from C₁ and C₂ at T_g by

      [math]\displaystyle{ \log \frac{\tau(T)}{\tau(T_{ref})} = \log a_T = - \frac{C_3(T-T_{ref})}{T-T_{ref}+C_4} }[/math]

where

      [math]\displaystyle{ C_3 = \frac{C_1C_2}{C_2+T_{ref}-T_g} \quad{\rm and}\quad C_4 = C_2+T_{ref}-T_g }[/math]

Material Properties

The unusual task for this material is to use multiple Gk and tauk properties (all with the same property name) to enter a material with multiple relaxation times.

Property	Description	Units	Default
pressureLaw	Picks the constitutive law used for time independent pressure. The options are 0 to linear elastic law and 1 to use MGEOS equation of state.	none	0
K	Time-independent bulk modulus (when using linear elastic law)	pressure units	none
(MGEOS)	Enter MGEOS properties C0, S1, S2, S3, gamma, and Kmax. The UJOption is fixed at 1.	varies	varies
G0	The long term (or fully-relaxed) shear modulus	pressure units	0
ntaus	The number of relaxation times. This property is only needed in XML files and must come before any Gk or tauk properties. In scripted files, the number is automatically determined from the number of relaxation times you provide.	none	none
Gk	The shear modulus for the next relaxation time. Enter multiple Gk properties to have multiple relaxation times.	pressure units	none
tauk	The next relaxation time. Enter multiple tauk properties to have multiple relaxation times.	time units	none
alpha	Thermal expansion coefficient (ignored when using MGEOS law)	ppm/K	40
(other)	Properties common to all materials	varies	varies

The total number of Gk and tauk properies must be equal. In XML files, that total number must match the supplied ntaus property.

The default value for Kmax is -1, which means to not limit the bulk modulus. This mode is almost always stable, but simulations with high compression should always add the AdjustTimeStep Custom Task to keep calculation stable under high tangent bulk modulus conditions.

Viscoelastic Solids and Liquids

If G0 is not zero, the material is a viscoelastic solid, which means the shear stress at infinite time reamains a finite number. Viscoelastic solids are used to model materials such as elastomers that do not show long time flow due to their cross links or have a plateau shear modulus equal to G0.

If G0 is zero, the material is a viscoelastic liquid that will flow like a liquid if you wait long enough. For example, to emulate a liquid (i.e., similar to a Tait Liquid Material), set G0 to zero, use a single relaxation time with tauk short (on time scale of the simulation), and set the one Gk modulus to:

      [math]\displaystyle{ G_1 = {\eta\over 2\tau_1} }[/math]

where [math]\displaystyle{ \eta }[/math] is desired viscosity and [math]\displaystyle{ \tau_1 }[/math] is the single relaxation time.

History Variables

This material tracks internal history variables (one for each relaxation time and each component of stress) for implementation of linear viscoelastic properties, but currently none of these internal variables are available for archiving.

This material also tracks J (total relative volume change) and J_res (volume change of free expansion state) as history variables 1 and 2. Note that J_res is only needed, and therefore only tracked, when using MGEOS for pressure constitutive law (when pressureLaw is 1). If not tracked, it is always 1.