Two-Phase Thermodynamic Equilibrium (TPTE) Model Reference

The Two-Phase Thermodynamic Equilibrium model is a simplified Multiphase Mixture implementation. This model is designed for applications that involve two phases of the same substance, typically water and steam, which are in thermodynamic equilibrium.

In this model, the computational effort is reduced by assuming the suspension to be a homogeneous single-phase system. The distribution of static enthalpy, and the assumption of thermodynamic equilibrium, are used to calculate the distribution of phases.

Table 1. Two-Phase Thermodynamic Equilibrium Model Reference
Theory See Two-Phase Thermodynamic Equilibrium.
Provided By [physics continuum] > Models > Multiphase Model
Example Node Path Continua > Physics 1 > Models > Two-Phase Thermodynamic Equilibrium
Requires
Pre-requisite selections:
  • Material: Multiphase
  • Multiphase Model: Two-Phase Thermodynamic Equilibrium

This model is compatible only with single-component phases.

Activates Physics Models

Automatically selected models:

Multiphase Interaction

Phase interaction models:

Two-Phase Equilibrium Interaction (activated automatically in a phase interaction)

Algebraic Slip (available for segregated flow only)

See Algebraic Slip Model Properties.

Drift Flux (available for both coupled flow and segregated flow)

See Drift Flux Model

Wall Boiling (the Gravity model must be activated in the physics continuum)

See Wall Boiling Models.

Materials

Dynamic Viscosity

Specific Heat

Thermal Conductivity

Turbulent Prandtl Number

See Materials and Methods.

Boundary Inputs See Boundary Settings.
Region Settings Physics Conditions:
  • Energy Source Option
  • Initial Condition Option
  • Momentum Source Option
  • Turbulence Source Option (for Turbulent viscous regimes)
See Region Settings.
Solvers

Segregated Flow

Segregated Energy

Coupled Implicit

Field Functions

Mass Fraction of [phase]

Specific Heat of [phase]

Thermal Conductivity of [phase]

Static Enthalpy at Saturation Temperature of [phase]

See Field Functions.

Algebraic Slip Model Properties

Velocity Ratio
Specifies the slip velocity ratio. This value is S in Eqn. (2954).

This value can be defined as a constant or as a field function (typically user-defined).

Drift Flux Model

The drift flux model takes into account the relative motion between phases by a constitutive relation. The energy contributions are limited to avoid sub-cooled water or superheated steam.
Under-Relaxation Factor
Under-relaxes both momentum and energy sources calculated by the drift flux model in Eqn. (2938) and Eqn. (2939). If the drift flux model is the suspected cause of numerical oscillations in the simulation, reduce this factor to aid stability. The default value is 1.0.
Max Acceleration Change
Limits the drift flux contribution to the momentum equations in Eqn. (2938). This expert property is expressed in terms of maximum acceleration threshold. This threshold represents the upper limit of the drift flux momentum source compared to a gravitational force. The default value is 10.0, which is considered to be a reasonable value for most cases.

The correlation in drift flux model is done by specifying the two parameters that define the drag force acting on the gas phase. These two parameters are:

Distribution Parameter

Specifies the distribution factor that reflects non-uniformity in the void fraction and velocity distribution. This value is C 0 in Eqn. (2944).

This value can be defined as a constant – a single three-part (or two-part for two-dimensional), comma-separated, number – or as a field function (typically user-defined).

Drift Velocity

Specifies the volume-weighted mean drift velocity. This value is v d r in Eqn. (2944).

This value can be defined as a constant, a field function (typically user-defined), or as a composite. A composite value has three components (for example, X, Y, Z) for three-dimensional problems, or two components (for example, X, Y) for two-dimensional problems.

Wall Boiling Models

The following wall boiling models are available:

Rohsenow Boiling
See Rohsenow Boiling Model Properties.
Transition Boiling
See Transition Boiling Model Properties.

Materials and Methods

Dynamic Viscosity
The dynamic (shear) viscosity of the fluid mixture is a measure of its resistance to shearing flows. This value is μ m in the formulation. Computed using the Volume-Weighted Mixture method.
Specific Heat

The specific heat of the fluid mixture is the ratio of the heat added to the mixture and the resulting temperature change. This value is C p in the formulation. Computed using the Mass-Weighted Mixture method.

See Phase Coupled Fluid Energy Model Reference.

Thermal Conductivity

The thermal conductivity of the fluid mixture is a measure of the ability of the mixture to conduct heat. This value is λ in the formulation. Computed using the Volume-Weighted Mixture method.

Turbulent Prandtl Number
The Turbulent Prandtl Number is the ratio of the momentum eddy diffusivity and the heat transfer eddy diffusivity in the fluid mixture. It is used in modeling heat transfer in turbulent boundary layer flows.

Activated when the Turbulent model is selected in the Viscous Regime.

Boundary Settings

No drift flux contributions are accounted for at inflow boundaries. An inflow boundary condition that includes a drift flux would imply that phase transfer (such as boiling or condensation) is taking place at the boundary. When using the Two-Phase Thermodynamic Equilibrium model, set the inflow boundary in a location where a homogeneous phase mixture enters the domain—not in a location where phase transfer occurs.

Inflow Boundaries
Volume Fraction
The ratio of the volume that each phase occupies to the computational cell volume.
When you specify boundary values, there is no restriction on the values that you can set for the volume fractions of the phases. However, Simcenter STAR-CCM+ uses normalized values for each phase volume fraction to ensure that the total volume fraction is 1.0.
Pressure Outlet
Volume Fraction
The ratio of the volume that each phase occupies to the computational cell volume.
  • This setting is relevant only when you have backflow. If you do not have backflow, ignore this setting.

  • If you have backflow, and only one phase is present at the pressure outlet, set the volume fraction of that phase to 1.

  • If you have backflow and a mixture of phases is present at the outlet, it is unlikely that the pressure outlet correctly captures your physics. (A pressure outlet assumes a constant pressure across the outflow interface.) You are advised to make your domain larger so that backflow no longer occurs.

Region Settings

Energy Source Option
Lets you specify energy source options for an individual region.

See Energy Source Option.

Initial Condition Option
Lets you customize initial conditions for an individual region.

See Setting Initial Conditions for a Particular Region.

Momentum Source Option
Method Corresponding Physics Value Nodes
Momentum Source Option
  • None

  • Specified

Adds a specified momentum source to the momentum equation.

When the Specified method is selected:

Momentum Source
Momentum Source Velocity Derivative

See Momentum Source Option.

Turbulence Source Option
Available when a turbulence model is activated in the physics continuum.
Method Corresponding Physics Value Nodes
Turbulence Source Option
  • None

  • Specified

  • Ambient

When the Specified method is selected:

Specific Dissipation Rate Source

Available for the K-Omega turbulence model.

See K-Omega Regions Reference.

Turbulent Kinetic Energy Source

Available for both the K-Omega and K-Epsilon turbulence models.

Turbulent Dissipation Rate Source

Available for the K-Epsilon turbulence model.

Turbulent Dissipation Rate Source Derivative

Available for the K-Epsilon turbulence model.

Turbulent Kinetic Energy Source Derivative

Available for the K-Epsilon turbulence model.

See K-Epsilon Regions Reference.

When the Ambient method is selected:

Ambient Turbulence Specification

Field Functions

Mass Fraction of [phase]
The ratio of the mass of the particular phase to the total mass in the cell.
Specific Heat of [phase]
Thermal Conductivity of [phase]
Static Enthalpy at Saturation Temperature of [phase]