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A new thermodynamic representation of binary electrolyte solutions nonideality in the whole range of concentrations
159
Citations
14
References
1978
Year
EngineeringElectrode-electrolyte InterfaceDissociation ConstantChemistryTheoretical ElectrochemistryIon ProcessSolution (Chemistry)Chemical EngineeringMolecular ThermodynamicsAnalytical ChemistryThermodynamicsElectrochemical InterfaceIon ExchangeNew Thermodynamic RepresentationPhysical ChemistryBorn Model ContributionWhole RangeDeep Eutectic SolventElectrochemistryIonic ConductorFundamental ElectrochemistryInterfacial PhenomenaChemical KineticsAcid Compositions
Abstract A system of equations based on the ionic atmosphere theory of Debye and Huckel, Born model contribution, and local compositions of the nonrandom two‐liquid (NRTL) model is developed to represent isothermal activity coefficients, in the whole range of concentrations, for solutions in an undissociated solvent of a partially or completely dissociated electrolyte. The physical constants and the four adjustable parameters necessary to represent the osmotic coefficient, for fifteen strong aqueous electrolytic solutions, are given at 298.15°K and atmospheric pressure. Vapor‐liquid equilibrium, for the hydrochloric acid‐water system at 298.15°K, is represented for acid compositions ranging from infinite dilution to 18 M using a known dissociation constant and six parameters.
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