For fixed composition, variable composition, and reacting mixtures,
for which mixture density is governed by the Ideal Mixture
option, the inverse of the mixture density is computed as a mass-fraction-weighted
average of specific volumes:
(1–34) |
When the global option for Mixture Properties is set to Non Ideal Mixture
, you can explicitly
set an equation of state for the mixture in the Mixture
Properties tab in the Material details
view. You may choose one of two options:
Mixture Density
Sets density as a function of pressure, temperature, and composition.
Mixture Pressure
Sets pressure as a function of specific volume, temperature, and composition.
For either option, the partial derivatives with respect to temperature
and pressure, for Mixture Density
, or temperature
and specific volume, for Mixture Pressure
, have
to be specified. CEL expressions may be used for defining the parameters
as functions of the mixture composition and the corresponding properties
of the mixture components. The following quantities are available
for use in the expressions:
Density: pressure, temperature, component mass fractions, component mole fractions, component molar masses, component densities, component specific volumes
d(rho)/dp at Const. T: pressure, temperature, component mass fractions, component mole fractions, component molar masses, component densities, component specific volumes, component density derivatives with respect to pressure at constant temperature
d(rho)/dT at Const. p: pressure, temperature, component mass fractions, component mole fractions, component molar masses, component densities, component specific volumes, component density derivatives with respect to temperature at constant pressure
Absolute Pressure: temperature, component mass fractions, component mole fractions, component molar masses, component densities, component specific volumes
dp/dv at Const. Temp.: pressure, temperature, component mass fractions, component mole fractions, component molar masses, component densities, component specific volumes, component pressure derivative with respect to volume at constant temperature
dp/dT at Const. Vol.: pressure, temperature, component mass fractions, component mole fractions, component molar masses, component densities, component specific volumes, component pressure derivative with respect to temperature at constant volume
The text boxes below provide CCL examples for the Mixture Density
and Mixture Pressure
options, respectively, for a mixture consisting of four components:
H2, O2, H2O, and N2. For simplicity the examples resemble the ideal
mixture rule, where for the Mixture Pressure
option
it is additionally assumed that all components are ideal gases.
EQUATION OF STATE: Option = Mixture Density Density = (H2.Mass Fraction/H2.Density + \ O2.Mass Fraction/O2.Density + \ H2O.Mass Fraction/H2O.Density + \ N2.Mass Fraction/N2.Density)^-1 drhodp t = (H2.Mass Fraction/H2.drhodp t + \ O2.Mass Fraction/O2.drhodp t + \ H2O.Mass Fraction/H2O.drhodp t + \ N2.Mass Fraction/N2.drhodp t)^-1 drhodt p = (H2.Mass Fraction/H2.drhodt p + \ O2.Mass Fraction/O2.drhodt p + \ H2O.Mass Fraction/H2O.drhodt p + \ N2.Mass Fraction/N2.drhodt p)^-1 END
EQUATION OF STATE: Option = Mixture Pressure Absolute Pressure = (H2.Mass Fraction/H2.Molar Mass + \ O2.Mass Fraction/O2.Molar Mass + \ H2O.Mass Fraction/H2O.Molar Mass + \ N2.Mass Fraction/N2.Molar Mass) * \ R*T / Specific Volume dpdv t = - (H2.Mass Fraction/H2.Molar Mass + \ O2.Mass Fraction/O2.Molar Mass + \ H2O.Mass Fraction/H2O.Molar Mass + \ N2.Mass Fraction/N2.Molar Mass) * \ R*T / (Specific Volume^2) dpdt v = (H2.Mass Fraction/H2.Molar Mass + \ O2.Mass Fraction/O2.Molar Mass + \ H2O.Mass Fraction/H2O.Molar Mass + \ N2.Mass Fraction/N2.Molar Mass) * \ R / Specific Volume END
It is your responsibility to ensure that the partial derivatives of density or pressure are consistent with the specific heat capacity definition. For details on consistency requirements, see General Equation of State in the CFX-Solver Theory Guide.