Solvation, surface excess free energy

Figure 4. Separation in methanol solutions with surface excess free energy e>f solvation at 0.005m and 1725 kPa...

The physicochemical criteria approach to reverse osmosis separations Involving the surface excess free energy of solvation for ionized and nonlonized solutes has been demonstrated by this work to include nonaqueous solutions. The parameters and correlations presented in this work permit the prediction of reverse osmosis separations and permeation rates for different alkali metal halides for cellulose acetate OEastman E-398) membranes of different surface porosities from only a single set of experimental data for a sodium chloride-methanol reference feed solution system. 

It should be noted that when replacing the London dispersive interactions term by other properties such as, for example, the air-hexadecane partition constant, by expressing the surface area in a more sophisticated way, and/or by including additional terms, the predictive capability could still be somewhat improved. From our earlier discussions, we should recall that we do not yet exactly understand all the molecular factors that govern the solvation of organic compounds in water, particularly with respect to the entropic contributions. It is important to realize that for many of the various molecular descriptors that are presently used in the literature to model yiw or related properties (see Section 5.5), it is not known exactly how they contribute to the excess free energy of the compound in aqueous solution. Therefore, when also considering that some of the descriptors used are correlated to each other (a fact that... 

---