AbstractFree volume theories for the concentration dependence of organic penetrant diffusion coefficients in rubbery amorphous polymers have been correlated and extended with emphasis given to similarities and mathematical equivalence for small volume fractions of penetrant. The nature of the empirical parameter used in VASENIN's theory has been further clarified by considering the kinetic and thermodynamic aspects of the plasticization effect. Using similar assumptions to those originally used for rubbery polymers, VASENIN's theory is extended to treat solvent diffusion in glassy and semi‐crystalline polymers. A procedure has been developed to extend the applicability of FUJITA's theory over a wider range of polymer‐solvent composition. The general effects of plasticization leading to increase in penetrant diffusion coefficients and decrease in polymeric glass transition temperatures are considered as resulting from the same functional increase in fractional free volume of a mixture with increasing solvent content. It is suggested that the two phenomena should be quantitatively compared for mutual consistency rather than attempting to develop a fully rigorous treatment for either. In this way diffusion data can be predicted from measurements of glass temperature depression or vice versa.