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Ionic fluid criticality chemical properties

To conclude this section on the DH theory, we would like to point out that these last two criticisms (neglecting short range repulsive interactions and linearizing the PBE) are the only valid criticisms. In fact the McMillan-Mayer theory (MMM) showed that, provided a correct definition of the "effective interaction potential" is given, the molecular structure of the solvent needs not to be considered explicitly(1) in calculating the thermodynamic properties of ionic solutions. This conclusion has very important consequences the first one is that, as the number density of ion in a typical electrolyte solutions is of the order of 10"3 ions/A, then the solution can be considered as a dilute ionic gas as a consequence the theories available for gases can be used for ionic fluids, provided the "effective potential" (more often called potential of the mean force at infinite dilution) takes the place ot the gas-gas interaction potential. Strictly this is true only in the limit of infinite dilution, but will hold also at finite concentrations, provided the chemical potential of the solvent in the given solution is the same as in the infinitely dilute solutions. This actually... [Pg.43]


See other pages where Ionic fluid criticality chemical properties is mentioned: [Pg.187]    [Pg.9]    [Pg.656]    [Pg.28]    [Pg.9]    [Pg.143]    [Pg.2927]    [Pg.86]    [Pg.680]   
See also in sourсe #XX -- [ Pg.2 ]




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