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CFX Multiphase 12.

0
Lecture 3

Modeling Approaches for


Multiphase Flow
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Overview
Training Manual

Full multiphase analyses


Eulerian-Eulerian: transport equation for volume fraction via continuity
equation for the dispersed phase; momentum equation for phases
Eulerian-Lagrangian: dispersed phases tracked as discrete trajectories;
ordinary differential equation (F = ma) for particle trajectory

Simplified multicomponent approaches


algebraic slip or drift flux model
equilibrium model for two-phase fluids with phase change
momentum equation for the single phase; either transport equations
(algebraic slip) or algebraic equations (equilibrium model) for the species mass fractions
representing the different phases

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Modeling Approaches
Training Manual

Different approaches can be used to model multiphase flows. The


suitability of a particular approach is determined by the nature
of the multiphase flow and the relevant physical phenomena.
Simplified multicomponent approaches
equilibrium model for two-phase fluids with phase change

mass transfer is assumed to be fast

volume fractions are determined as algebraic expressions based on


the energy of the mixture and the liquid and vapor enthalpies
mixture properties are calculated given the volume fractions
and the liquid and vapor properties

algebraic slip or drift flux model


particles are assumed to reach their terminal velocity instantaneously (small
particles, nondrag forces negligible)
algebraic slip phases are modeled as mass fractions

Full multiphase analyses


Eulerian-Eulerian: transport equation for volume fraction
Eulerian-Lagrangian: dispersed phases tracked as discrete trajectories
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Eulerian-Eulerian Approach
Training Manual

Phases form interpenetrating continua


Phases mixed at length scales larger than molecules. However, mixing
is at scales smaller than we wish to resolve.
The phases share the same volume in space. Each phase is assumed
present in each control volume (cell) and assigned a volume fraction
equal to the fraction of the volume occupied. Volume fractions will be
determined by solution of the continuity equation for each phase.
In general, each phase has its own field variables. Variables which
are assumed to be homogeneous will be shared between phases
The phases are coupled by inter-phase models for energy, additional
variable (mass), and momentum transfer.
Inter-phase transfer models are provided as empirical input to the
problem specification and are highly problem dependent.

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Eulerian-Eulerian Approach
Training Manual

Continuity, momentum, energy, and general scalar conservation


equations for each phase.
N sets of coupled partial differential equations

(u, v, w, p, T, vf)1
(u, v, w, p, T, vf)2

(u, v, w, p, T, vf)N
6 + 6 + unknowns
5 + 5 + 5 equations
vf1+vf2 + = 1

p1=p2=pN
In the homogeneous treatment, the two phases are assumed to share
all field variables except for volume fraction - less computational
overhead, often used for free surface problems
In the inhomogeneous treatment, only the pressures are shared
between phases
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Effect of Averaging
Training Manual

Generally, we assume that any given cell contains a number of


dispersed phase particles, droplets, or bubbles. The amount of a
dispersed phase contained in any given cell is quantified
according to its volume fraction.
We are introducing phase-weighted averaging
Discrete particles, droplets, ... statistic probability (volume fraction)
Interface structure not available after averaging

1 0.5

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Eulerian Transport Equation


Training Manual

Transport equation for a general variable. These equations have the


same form as they would for a single phase flow except that they
have been weighted by volume fraction r and interphase transfer terms
have been added:

( r ) ( rU r ) r S T
t
There are two sets of source terms on the right-hand side. The first is a
standard volume fraction weighted source term. The second represents
interphase transfer.
For two phase flows:

T1 c12 (2 1 )
where
c12 (2 1 ) is the interphase transfer term due to exchange of
energy (heat) or momentum (drag)
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Continuity and Momentum


Training Manual

Phasic continuity equation:


NP

( r ) ( rU ) ( m m )
t
1

Momentum equation:

( r U ) [r { U U (U [U ]T )}]
t
r ( B p ) c U U
NP

A variety of models for the interphase drag coefficient are built into
ANSYS CFX and users can specify their own model.
The continuity equation given above shows interphase mass
transfer terms on the right hand side.
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MUSIG Model
Training Manual

In the standard Eulerian-Eulerian implementation, a dispersed phase


is characterized by a single diameter. In many cases, for fluid
droplets and bubbles, the dispersed phase diameter may change due
to coalescence or dispersion induced by fluid forces.
MUSIG Model
Multiple Size Group model
The dispersed phase is divided up into a number of size groups
Accounts for coalescence and breakup in polydispersed phases using
population balance approach
In the default homogeneous treatment, all size groups are
assumed to move with the same velocity
The distribution of the dispersed phase among the different size groups is
predicted by the simulation, which allows the local mean size and
interfacial area to change in response to fluid forces and the processes of
coalescence and dispersion
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Eulerian-Lagrangian Approach
Training Manual

In the Eulerian-Lagrangian approach, the continuous phase is


treated in the manner previously described, but one or more
dispersed phases are tracked as a number of representative
particle trajectories

For an Eulerian phase, we solve PDEs for all dependent variables


(velocity, temperature, etc.)

For a Lagrangian phase, we solve ODEs for the motion of


particles which are treated as moving mass points:
F = ma = m d2X/dt2

Eulerian and Lagrangian phases still interact by exchanging


momentum, energy, and mass

Changes in particle size are convenient to model with the


Lagrangian approach
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Force Balance on a Single Particle

Training Manual

Particle momentum equation


balance of aerodynamic and body forces

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Single Particle Forces

Drag
Buoyancy
System rotation
Added mass
Pressure gradient
Basset

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Training Manual

1
FD C D C AP U P U C U P U C
2
r
r
FB M P P C P g



FR 2 U P P rP P
r
r
r
1
FVM CVM M C dU C dt dU P dt
2
r
r
FP M C dU C dt M C P C

r
FBH History of acceleration

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Algebraic Slip Model


Training Manual

Simplified multicomponent multiphase model


Use algebraic equation for slip/drift velocities
See solver theory documentation for derivation

Advantages:
Reduced CPU time
Reduced numerical complexity

Limitations:
Dispersed phase must be of low density or small diameter
(assumes terminal velocity is reached instantaneously)
Nondrag forces are negligible

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Algebraic Slip Model in ANSYS CFX


Training Manual

Implementation in ANSYS CFX


Single-phase multi-component model
Set continuous phase as constraint component
Set each dispersed phase as Algebraic Slip components. Choose
either:

Drag force balance - slip velocity calculated by solver, given a


particular drag law (eg, Schiller Naumann).
Slip velocity if you want to use a custom drag law

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Algebraic Slip Model in ANSYS CFX


Training Manual

Turbulent dispersion
Modeled using standard gradient diffusion hypothesis, controlled by
turbulent Prandtl number

Energy equation consistency


Energy transported by drift flows is also modeled.

Wall deposition
Walls can be set as deposition walls. Dispersed phases are
removed from system, replaced by constraint component.
Deposition rate available for post-processing.

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Algebraic Slip Model in ANSYS CFX


Training Manual

Post-processing variables:
Mass fraction
Volume fraction
Deposition rate
Slip velocity
Drift velocity

Model restrictions
The continuous and dispersed phases cannot themselves be
variable composition mixtures

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Algebraic Slip Model Example


Training Manual

Example:
L-bend, joined by GGI
Gravity in x-direction
Deposition wall on side and bottom
Three particle groups:
Small: 1.E-6 [m]
Medium: 1.E-5 [m]
Large: 1.E-4 [m]

Schiller-Naumann drag law

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Algebraic Slip Model Example


Training Manual

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Algebraic Slip Model Example


Training Manual

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Algebraic Slip Model Example


Training Manual

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Algebraic Slip Model Example


Training Manual

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Equilibrium Multiphase Models


Training Manual

In some cases, we may not be interested in a detailed description


of the two-phase flow behavior, but we would like to use accurate
properties for the two-phase mixture

An example would be flow of wet steam or a refrigerant vapor.

In the equilibrium approach we assume that the two-phase mixture is in


equilibrium with the quality of the mixture determined by the enthalpy of
the mixture and the enthalpies of the individual liquid phases:
x = (hmixture - hl)/(hv - hl)

The saturation properties of the mixture must be defined by creating a


Homogeneous Binary Mixture

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Equilibrium Multiphase Models


Training Manual

The homogenous binary mixture defines the saturation


properties of the two components (i.e. liquid and vapor) which
comprise the mixture
The homogeneous binary mixture is used as the single fluid
in the definition of the flow domain
One of the components (i.e. liquid or vapor) is specified as the
equlibrium fraction for which a transport equation is solved while the
other component is set as the equilibrium constraint.

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Equilibrium Model Example


Training Manual

Importing materials from the IAPWS Model library (Water/Steam)

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Equilibrium Model Example


Training Manual

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Equilibrium Model Example


Training Manual

Homogeneous
Binary Mixture

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Equilibrium Model Example


Training Manual

Homogeneous
Binary Mixture

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IAPWS Properties of Water and Steam


Training Manual

IAPWS-IF97 equation-of-state first implemented in ANSYS CFX 11.0


Reference: W. Wagner, A. Kruse:
The Industrial Standard IAPWS-IF97: Properties of Water and Steam, Springer, Berlin, 1998

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1.

subcooled water

2.

supercritical water/steam

3.

superheated steam

4.

saturation data

5.

high temperature steam


(currently not implemented in
IAPWS library in CFX, but
properties at high T, low P can
be evaluated with Ideal Gas
Law)
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IAPWS Properties of Water and Steam


Training Manual

Liquid water and steam selectable from


IAPWS database
CFX uses a look-up table approach for
speed of computation so an appropriate
(T,p) range should be specified and
extrapolation or clipping should be
selected for conditions that lie outside
the range
Library contains data for density, heat
capacity, thermal conductivity, and
viscosity of phases
IAPWS library includes entry for
Homogeneous Binary Mixture for
water/steam pairs as well:
Acts a placeholder for phase pair related
properties, i.e. Tsat=Tsat(p) and =(T)

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Extrapolation and Clipping


Training Manual

If table range values are poorly chosen, then properties may be based on clipped
or extrapolated property data, which can be bad in terms of both robustness and
accuracy
Sometimes the out-of-range errors occur near the start of the run, but go away as
a converged solution is approached. In other cases, if there are conditions in the
simulation which lie outside the table range, the out-of-range messages can
persist through to the final solution
The solver will write out diagnostic messages to the output file with appropriate
suggestions when clipping or extrapolation takes place:
+--------------------------------------------------------------------+
|
****** Notice ******
|
| While evaluating Water.Density,
|
| Water.Static Temperature on domain Default Domain
|
| went outside of its lower limit. Its minimum value was
|
| 3.7300E+02. The bounds error was handled by clipping.
|
| If this situation persists, consider increasing the table range.
|
+--------------------------------------------------------------------+

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Importing Materials from the IAPWS Library


Training Manual

To import materials from the IAPWS,


right-click on Materials and choose
to Import from Library. On the
Import CCL form, scroll through the list
of available libraries and choose the
IAPWS library.
There are several predefined liquid,
vapor, and homogeneous binary
mixture materials in the IAPWS library.
Since all materials in
the library obey the IAPWS EOS, the
different materials really just
correspond to different preset
temperature and pressure
ranges. The table range can always be
modified in CFX-Pre, even for one of
the predefined materials.

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IAPWS Table Ranges


#

Liquid

Vapor

T (K)

P (Pa)

273-450 620100K

373-700 100K-500K

273-550 100200K

420-900 500K-1000K

450-900 100K-30000K

HBM

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Training Manual

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