MargulesVPSSTP.h

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/**
 *  @file  MargulesVPSSTP.h (see @ref thermoprops and class @link
 *      Cantera::MargulesVPSSTP MargulesVPSSTP@endlink).
 */
 
// This file is part of Cantera. See License.txt in the top-level directory or
// at https://cantera.org/license.txt for license and copyright information.
 
#ifndef CT_MARGULESVPSSTP_H
#define CT_MARGULESVPSSTP_H
 
#include "GibbsExcessVPSSTP.h"
 
namespace Cantera
{
 
//! MargulesVPSSTP is a derived class of GibbsExcessVPSSTP that employs the
//! Margules approximation for the excess Gibbs free energy
/*!
 * MargulesVPSSTP derives from class GibbsExcessVPSSTP which is derived from
 * VPStandardStateTP, and overloads the virtual methods defined there with ones
 * that use expressions appropriate for the Margules Excess Gibbs free energy
 * approximation.
 *
 * The independent unknowns are pressure, temperature, and mass fraction.
 *
 * ## Specification of Species Standard State Properties
 *
 * All species are defined to have standard states that depend upon both the
 * temperature and the pressure. The Margules approximation assumes symmetric
 * standard states, where all of the standard state assume that the species are
 * in pure component states at the temperature and pressure of the solution.  I
 * don't think it prevents, however, some species from being dilute in the
 * solution.
 *
 * ## Specification of Solution Thermodynamic Properties
 *
 * The molar excess Gibbs free energy is given by the following formula which is
 * a sum over interactions *i*. Each of the interactions are binary interactions
 * involving two of the species in the phase, denoted, *Ai* and *Bi*. This is
 * the generalization of the Margules formulation for a phase that has more than
 * 2 species.
 *
 * @f[
 *     G^E = \sum_i \left(  H_{Ei} - T S_{Ei} \right)
 * @f]
 * @f[
 *    H^E_i = n X_{Ai} X_{Bi} \left( h_{o,i} +  h_{1,i} X_{Bi} \right)
 * @f]
 * @f[
 *    S^E_i = n X_{Ai} X_{Bi} \left( s_{o,i} +  s_{1,i} X_{Bi} \right)
 * @f]
 *
 * where n is the total moles in the solution.
 *
 * The activity of a species defined in the phase is given by an excess Gibbs
 * free energy formulation.
 *
 * @f[
 *      a_k = \gamma_k  X_k
 * @f]
 *
 * where
 *
 * @f[
 *      R T \ln( \gamma_k )= \frac{d(n G^E)}{d(n_k)}\Bigg|_{n_i}
 * @f]
 *
 * Taking the derivatives results in the following expression
 *
 * @f[
 *      R T \ln( \gamma_k )= \sum_i \left( \left( \delta_{Ai,k} X_{Bi} + \delta_{Bi,k} X_{Ai}  - X_{Ai} X_{Bi} \right)
 *       \left( g^E_{o,i} +  g^E_{1,i} X_{Bi} \right) +
 *       \left( \delta_{Bi,k} - X_{Bi} \right)      X_{Ai} X_{Bi}  g^E_{1,i} \right)
 * @f]
 * where
 * @f$  g^E_{o,i} =  h_{o,i} - T s_{o,i} @f$ and
 * @f$ g^E_{1,i} =  h_{1,i} - T s_{1,i} @f$ and where
 * @f$ X_k @f$ is the mole fraction of species *k*.
 *
 * This object inherits from the class VPStandardStateTP. Therefore, the
 * specification and calculation of all standard state and reference state
 * values are handled at that level. Various functional forms for the standard
 * state are permissible. The chemical potential for species *k* is equal to
 *
 * @f[
 *      \mu_k(T,P) = \mu^o_k(T, P) + R T \ln(\gamma_k X_k)
 * @f]
 *
 * The partial molar entropy for species *k* is given by
 *
 * @f[
 *       \tilde{s}_k(T,P) =  s^o_k(T,P)  - R \ln( \gamma_k X_k )
 *              - R T \frac{d \ln(\gamma_k) }{dT}
 * @f]
 *
 * The partial molar enthalpy for species *k* is given by
 *
 * @f[
 *      \tilde{h}_k(T,P) = h^o_k(T,P) - R T^2 \frac{d \ln(\gamma_k)}{dT}
 * @f]
 *
 * The partial molar volume for species *k* is
 *
 * @f[
 *        \tilde V_k(T,P)  = V^o_k(T,P)  + R T \frac{d \ln(\gamma_k) }{dP}
 * @f]
 *
 * The partial molar Heat Capacity for species *k* is
 *
 * @f[
 *      \tilde{C}_{p,k}(T,P) = C^o_{p,k}(T,P)   - 2 R T \frac{d \ln( \gamma_k )}{dT}
 *              - R T^2 \frac{d^2 \ln(\gamma_k) }{{dT}^2}
 * @f]
 *
 * ## Application within Kinetics Managers
 *
 * @f$ C^a_k @f$ are defined such that @f$ a_k = C^a_k / C^s_k, @f$ where
 * @f$ C^s_k @f$ is a standard concentration defined below and @f$ a_k @f$ are
 * activities used in the thermodynamic functions.  These activity (or
 * generalized) concentrations are used by kinetics manager classes to compute
 * the forward and reverse rates of elementary reactions. The activity
 * concentration,@f$  C^a_k @f$,is given by the following expression.
 *
 * @f[
 *      C^a_k = C^s_k  X_k  = \frac{P}{R T} X_k
 * @f]
 *
 * The standard concentration for species *k* is independent of *k* and equal to
 *
 * @f[
 *     C^s_k =  C^s = \frac{P}{R T}
 * @f]
 *
 * For example, a bulk-phase binary gas reaction between species j and k,
 * producing a new gas species l would have the following equation for its rate
 * of progress variable, @f$ R^1 @f$, which has units of kmol m-3 s-1.
 *
 * @f[
 *    R^1 = k^1 C_j^a C_k^a =  k^1 (C^s a_j) (C^s a_k)
 * @f]
 * where
 * @f[
 *    C_j^a = C^s a_j \mbox{\quad and \quad} C_k^a = C^s a_k
 * @f]
 *
 * @f$ C_j^a @f$ is the activity concentration of species j, and @f$ C_k^a @f$
 * is the activity concentration of species k. @f$ C^s @f$ is the standard
 * concentration. @f$ a_j @f$ is the activity of species j which is equal to the
 * mole fraction of j.
 *
 * The reverse rate constant can then be obtained from the law of microscopic
 * reversibility and the equilibrium expression for the system.
 *
 * @f[
 *       \frac{a_j a_k}{ a_l} = K_a^{o,1} = \exp(\frac{\mu^o_l - \mu^o_j - \mu^o_k}{R T} )
 * @f]
 *
 * @f$  K_a^{o,1} @f$ is the dimensionless form of the equilibrium constant,
 * associated with the pressure dependent standard states @f$ \mu^o_l(T,P) @f$
 * and their associated activities, @f$ a_l @f$, repeated here:
 *
 * @f[
 *      \mu_l(T,P) = \mu^o_l(T, P) + R T \ln a_l
 * @f]
 *
 * We can switch over to expressing the equilibrium constant in terms of the
 * reference state chemical potentials
 *
 * @f[
 *     K_a^{o,1} = \exp(\frac{\mu^{ref}_l - \mu^{ref}_j - \mu^{ref}_k}{R T} ) * \frac{P_{ref}}{P}
 * @f]
 *
 * The concentration equilibrium constant, @f$ K_c @f$, may be obtained by
 * changing over to activity concentrations. When this is done:
 *
 * @f[
 *       \frac{C^a_j C^a_k}{ C^a_l} = C^o K_a^{o,1} = K_c^1 =
 *           \exp(\frac{\mu^{ref}_l - \mu^{ref}_j - \mu^{ref}_k}{R T} ) * \frac{P_{ref}}{RT}
 * @f]
 *
 * %Kinetics managers will calculate the concentration equilibrium constant, @f$
 * K_c @f$, using the second and third part of the above expression as a
 * definition for the concentration equilibrium constant.
 *
 * For completeness, the pressure equilibrium constant may be obtained as well
 *
 * @f[
 *     \frac{P_j P_k}{ P_l P_{ref}} = K_p^1 = \exp(\frac{\mu^{ref}_l - \mu^{ref}_j - \mu^{ref}_k}{R T} )
 * @f]
 *
 * @f$ K_p @f$ is the simplest form of the equilibrium constant for ideal gases.
 * However, it isn't necessarily the simplest form of the equilibrium constant
 * for other types of phases; @f$ K_c @f$ is used instead because it is
 * completely general.
 *
 * The reverse rate of progress may be written down as
 * @f[
 *    R^{-1} = k^{-1} C_l^a =  k^{-1} (C^o a_l)
 * @f]
 *
 * where we can use the concept of microscopic reversibility to write the
 * reverse rate constant in terms of the forward rate constant and the
 * concentration equilibrium constant, @f$ K_c @f$.
 *
 * @f[
 *    k^{-1} =  k^1 K^1_c
 * @f]
 *
 * @f$ k^{-1} @f$ has units of s-1.
 *
 * @ingroup thermoprops
 */
class MargulesVPSSTP : public GibbsExcessVPSSTP
{
public:
    //! Construct a MargulesVPSSTP object from an input file
    /*!
     * @param inputFile Name of the input file containing the phase definition.
     *                  If blank, an empty phase will be created.
     * @param id        name (ID) of the phase in the input file. If empty, the
     *                  first phase definition in the input file will be used.
     */
    explicit MargulesVPSSTP(const string& inputFile="", const string& id="");
 
    string type() const override {
        return "Margules";
    }
 
    //! @name  Molar Thermodynamic Properties
    //! @{
 
    double enthalpy_mole() const override;
    double entropy_mole() const override;
    double cp_mole() const override;
    double cv_mole() const override;
 
    //! @}
    //! @name Activities, Standard States, and Activity Concentrations
    //!
    //! The activity @f$ a_k @f$ of a species in solution is related to the
    //! chemical potential by @f[ \mu_k = \mu_k^0(T) + \hat R T \ln a_k. @f] The
    //! quantity @f$ \mu_k^0(T,P) @f$ is the chemical potential at unit activity,
    //! which depends only on temperature and pressure.
    //! @{
 
    void getLnActivityCoefficients(double* lnac) const override;
 
    //! @}
    //! @name  Partial Molar Properties of the Solution
    //! @{
 
    void getChemPotentials(double* mu) const override;
 
    //! Returns an array of partial molar enthalpies for the species in the
    //! mixture.
    /*!
     * Units (J/kmol)
     *
     * For this phase, the partial molar enthalpies are equal to the standard
     * state enthalpies modified by the derivative of the molality-based
     * activity coefficient wrt temperature
     *
     * @f[
     *   \bar h_k(T,P) = h^o_k(T,P) - R T^2 \frac{d \ln(\gamma_k)}{dT}
     * @f]
     *
     * @param hbar  Vector of returned partial molar enthalpies
     *              (length m_kk, units = J/kmol)
     */
    void getPartialMolarEnthalpies(double* hbar) const override;
 
    //! Returns an array of partial molar entropies for the species in the
    //! mixture.
    /*!
     * Units (J/kmol)
     *
     * For this phase, the partial molar enthalpies are equal to the standard
     * state enthalpies modified by the derivative of the activity coefficient
     * wrt temperature
     *
     * @f[
     *   \bar s_k(T,P) = s^o_k(T,P) - R T^2 \frac{d \ln(\gamma_k)}{dT}
     *                              - R \ln( \gamma_k X_k)
     *                              - R T \frac{d \ln(\gamma_k) }{dT}
     * @f]
     *
     * @param sbar  Vector of returned partial molar entropies
     *              (length m_kk, units = J/kmol/K)
     */
    void getPartialMolarEntropies(double* sbar) const override;
 
    //! Returns an array of partial molar entropies for the species in the
    //! mixture.
    /*!
     * Units (J/kmol)
     *
     * For this phase, the partial molar enthalpies are equal to the standard
     * state enthalpies modified by the derivative of the activity coefficient
     * wrt temperature
     *
     *  @f[
     *   ???????????????
     *   \bar s_k(T,P) = s^o_k(T,P) - R T^2 \frac{d \ln(\gamma_k)}{dT}
     *                              - R \ln( \gamma_k X_k)
     *                              - R T \frac{d \ln(\gamma_k) }{dT}
     *   ???????????????
     *  @f]
     *
     * @param cpbar  Vector of returned partial molar heat capacities
     *              (length m_kk, units = J/kmol/K)
     */
    void getPartialMolarCp(double* cpbar) const override;
 
    void getPartialMolarVolumes(double* vbar) const override;
 
    //! Get the array of temperature second derivatives of the log activity
    //! coefficients
    /*!
     *  units = 1/Kelvin
     *
     * @param d2lnActCoeffdT2  Output vector of temperature 2nd derivatives of
     *                         the log Activity Coefficients. length = m_kk
     */
    void getd2lnActCoeffdT2(double* d2lnActCoeffdT2) const;
 
    void getdlnActCoeffdT(double* dlnActCoeffdT) const override;
 
    //! @}
    //! @name Initialization
    //!
    //! The following methods are used in the process of constructing the phase
    //! and setting its parameters from a specification in an input file. They
    //! are not normally used in application programs. To see how they are used,
    //! see importPhase()
    //! @{
 
    void initThermo() override;
    void getParameters(AnyMap& phaseNode) const override;
 
    //! Add a binary species interaction with the specified parameters
    /*!
     * @param speciesA   name of the first species
     * @param speciesB   name of the second species
     * @param h0         first excess enthalpy coefficient [J/kmol]
     * @param h1         second excess enthalpy coefficient [J/kmol]
     * @param s0         first excess entropy coefficient [J/kmol/K]
     * @param s1         second excess entropy coefficient [J/kmol/K]
     * @param vh0        first enthalpy coefficient for excess volume [m^3/kmol]
     * @param vh1        second enthalpy coefficient for excess volume [m^3/kmol]
     * @param vs0        first entropy coefficient for excess volume [m^3/kmol/K]
     * @param vs1        second entropy coefficient for excess volume [m^3/kmol/K]
     */
    void addBinaryInteraction(const string& speciesA,
        const string& speciesB, double h0, double h1, double s0, double s1,
        double vh0, double vh1, double vs0, double vs1);
 
    //! @}
    //! @name  Derivatives of Thermodynamic Variables needed for Applications
    //! @{
 
    void getdlnActCoeffds(const double dTds, const double* const dXds,
                          double* dlnActCoeffds) const override;
    void getdlnActCoeffdlnX_diag(double* dlnActCoeffdlnX_diag) const override;
    void getdlnActCoeffdlnN_diag(double* dlnActCoeffdlnN_diag) const override;
    void getdlnActCoeffdlnN(const size_t ld, double* const dlnActCoeffdlnN) override;
 
    //! @}
 
private:
    //! Initialize lengths of local variables after all species have been
    //! identified.
    void initLengths();
 
    //! Update the activity coefficients
    /*!
     * This function will be called to update the internally stored natural
     * logarithm of the activity coefficients
     */
    void s_update_lnActCoeff() const;
 
    //! Update the derivative of the log of the activity coefficients wrt T
    /*!
     * This function will be called to update the internally stored derivative
     * of the natural logarithm of the activity coefficients wrt temperature.
     */
    void s_update_dlnActCoeff_dT() const;
 
    //! Update the derivative of the log of the activity coefficients wrt
    //! log(mole fraction)
    /*!
     * This function will be called to update the internally stored derivative
     * of the natural logarithm of the activity coefficients wrt logarithm of
     * the mole fractions.
     */
    void s_update_dlnActCoeff_dlnX_diag() const;
 
    //! Update the derivative of the log of the activity coefficients wrt
    //! log(moles) - diagonal only
    /*!
     * This function will be called to update the internally stored diagonal
     * entries for the derivative of the natural logarithm of the activity
     * coefficients wrt logarithm of the moles.
     */
    void s_update_dlnActCoeff_dlnN_diag() const;
 
    //! Update the derivative of the log of the activity coefficients wrt
    //! log(moles_m)
    /*!
     * This function will be called to update the internally stored derivative
     * of the natural logarithm of the activity coefficients wrt logarithm of
     * the mole number of species
     */
    void s_update_dlnActCoeff_dlnN() const;
 
protected:
    //! number of binary interaction expressions
    size_t numBinaryInteractions_ = 0;
 
    //! Enthalpy term for the binary mole fraction interaction of the
    //! excess Gibbs free energy expression
    mutable vector<double> m_HE_b_ij;
 
    //! Enthalpy term for the ternary mole fraction interaction of the
    //! excess Gibbs free energy expression
    mutable vector<double> m_HE_c_ij;
 
    //! Entropy term for the binary mole fraction interaction of the
    //! excess Gibbs free energy expression
    mutable vector<double> m_SE_b_ij;
 
    //! Entropy term for the ternary mole fraction interaction of the
    //! excess Gibbs free energy expression
    mutable vector<double> m_SE_c_ij;
 
    //! Enthalpy term for the binary mole fraction interaction of the
    //! excess Gibbs free energy expression
    mutable vector<double> m_VHE_b_ij;
 
    //! Enthalpy term for the ternary mole fraction interaction of the
    //! excess Gibbs free energy expression
    mutable vector<double> m_VHE_c_ij;
 
    //! Entropy term for the binary mole fraction interaction of the
    //! excess Gibbs free energy expression
    mutable vector<double> m_VSE_b_ij;
 
    //! Entropy term for the ternary mole fraction interaction of the
    //! excess Gibbs free energy expression
    mutable vector<double> m_VSE_c_ij;
 
    //! vector of species indices representing species A in the interaction
    /*!
     *  Each Margules excess Gibbs free energy term involves two species, A and
     *  B. This vector identifies species A.
     */
    vector<size_t> m_pSpecies_A_ij;
 
    //! vector of species indices representing species B in the interaction
    /*!
     *  Each Margules excess Gibbs free energy term involves two species, A and
     *  B. This vector identifies species B.
     */
    vector<size_t> m_pSpecies_B_ij;
 
    //! form of the Margules interaction expression
    /*!
     *  Currently there is only one form.
     */
    int formMargules_ = 0;
 
    //! form of the temperature dependence of the Margules interaction expression
    /*!
     *  Currently there is only one form -> constant wrt temperature.
     */
    int formTempModel_ = 0;
};
 
}
 
#endif