PSRK (short for Predictive Soave-Redlich-Kwong) is an estimation method for the calculation of phase equilibria of mixtures of chemical components. The original goal for the development of this method was to enable the estimation of properties of mixtures which contain supercritical components. This class of substances cannot be predicted with established models, for example UNIFAC.
PSRK is a group contribution equation of state. This is a class of prediction methods which combines equations of state (mostly cubic) with activity coefficient models based on group contributions, such as UNIFAC. The activity coefficient model is used to adapt the equation of state parameters for mixtures by a so-called mixing rule.
The use of an equation of state introduces all thermodynamic relations defined for equations of state into the PRSK model. This allows the calculation of densities, enthalpies, heat capacities, and other properties.
As stated previously, the PSRK model is based on a combination of the Soave-Redlich-Kwong equation of state with a mixing rule whose parameters are determined by the UNIFAC method.
Equation of State
The equation of state of Soave is defined as follows:
The original α-function has been replaced by the function of Mathias-Copeman .
The parameters of the Mathias-Copeman equation are fitted to experimental vapor pressure data of pure components and provide a better description of the vapor pressure than the original relation. The form of the equation is chosen as it can be reduced to the original Soave form by setting the parameters c2 und c3 to zero. Additionally, the parameter c1 can be obtained from the acentric factor, using the relation:
This may be performed if no fitted Mathias-Copeman parameter is available.
The PSRK mixing rule calculates the parameters a and b of the equation of state by
Where the parameters ai and bi are those of the pure substances, their mole fractions are given by xi and the excess Gibbs energy gE. The excess Gibbs energy is calculated by a slightly modified UNIFAC model.
The integrity of the model can be improved if the acentric factor is replaced by Mathias-Copeman constants which have been fitted to experimental vapor pressure data of pure components.
The mixing rule uses UNIFAC which needs a variety of UNIFAC-specific parameters. Aside from some model constants, the most important parameters are the group interaction parameters --- these are obtained from parametric fits to experimental vapor-liquid equilibria of mixtures.
Hence, for high-quality model parameters experimental data (pure component vapor pressures and VLE of mixtures) are needed. These are normally provided by factual data banks like the Dortmund Data Bank which has been the base for the PSRK development. In few cases additionally needed data have been determined experimentally if no data have been available from other sources.
The prediction of a vapor-liquid equilibrium is successful even in mixtures containing supercritical components.
However, the mixture has to be subcritical. In the given example carbon dioxide is the supercritical component with Tc=304.19 K and Pc=7475 kPa. The critical point of the mixture lies at T=411 K and P≈15000 kPa. The composition of the mixture is near 78 mole% carbon dioxide and 22 mole% cyclohexane.
- The gradient of the Mathias-Copeman α-function is without any thermodynamic background and, if extrapolated to higher temperatures, the described vapor pressure curve tends to diverge.
- The Soave-Redlich-Kwong equation of state describes the vapor densities of pure components and mixtures quite well but the deviations of the liquid density prediction are high.
- For the VLE prediction of mixtures with components which have very differing sizes (e. g. Ethanol, C2H6O, and Eicosane, C20H44) larger systematic errors are found.
- Heats of mixing and activity coefficients at infinite dilution are predicted poorly.
- Holderbaum T., “Die Vorausberechnung von Dampf-Flüssig-Gleichgewichten mit einer Gruppenbeitragszustandsgleichung”, Fortschrittsber. VDI Reihe 3, 243, 1-154, 1991
- Mathias P.M., Copeman T.W., “Extension of the Peng-Robinson Equation of State to Complex Mixtures: Evaluation of the Various Forms of the Local Composition Concept”, Fluid Phase Equilib., 13, 91-108, 1983. ISSN 0378-3812, doi:10.1016/0378-3812(83)80084-3
- Horstmann S., Jabloniec A., Krafczyk J., Fischer K., Gmehling J., “PSRK Group Contribution Equation of State: Comprehensive Revision and Extension IV, Including Critical Constants and a-Function Parameters for 1000 Components”, Fluid Phase Equilib., 227(2), 157-164, 2005
- Ambrose D., Trans. Faraday Soc., 52, 772-781, 1956. ISSN 0014-7672, doi:10.1039/TF9565200772
- Schmidt E., Thomas W., Forsch. Geb. Ingenieurwes. Ausg. A , 20, 161-170, 1954
- Ahlers J., “Entwicklung einer universellen Gruppenbeitragszustandsgleichung”, Thesis, Carl-von-Ossietzky-Universität Oldenburg, 1-144, 2003