Menzles, M. A. Can. J . Chem. Eng. 1971, 49, 407. Lenhoff, A. M.; Morarl, M. Chem. Eng. Sci. 1982, 37, 245. Null, H. R. Chem. Eng. frog. 1978. 72. 58. Rathore, R. N. S.; Van Wormer, K. A.; Powers, 0. J. AIChE J . 1974, 20, Robertson, J. C. Chem. Eng. 1974, 81, 104. Roblnscn, C. S.; ollllland, E. R. "Elements of Fractional Distillation", 4th ed.; Tyreus, 8. D.; Luyben, W. L. /fydrmrbon frocess. 1975, 54. 93.Data on the reverse osmosls separations of Inorganic electrolytes and organic nonelectrolytes from methanol solutions were generated together with corresponding liquid chromatography data. Transport equations based on the surface force-pore flow model for reverse osmosis were applied to calculate the force constants associated with steric hindrance, electrostatic repulsion, and van der Waals attraction. These constants enable prediction of the separations of inorganic and the organic solutes studled when the pore radius of a membrane Is given. The solute separations from methanol solutlons were compared with those from aqueous solutions by use of the data from membranes of nearly equal effective pore sizes. The formation of agglomerates enhances the separation from the aqueous solution, particularly In the case of hydrocarbon solutes. The interfacial solvation and the consequentlal steric repulsion at the Interface are higher for cations of higher charge densky and lower for cations of lower charge density In methanol solvent systems compared to aqueous solvent systems.