Journal of Polymer Science Part B: Polymer Physics, Vol.38, No.19, 2525-2536, 2000
Relationships between the chemical structures and the solubility, diffusivity, and permselectivity of propylene and propane in 6FDA-based polyimides
The solubility, diffusivity, and permselectivity of propylene and propane in 40 different polyimides synthesized from 2,2-bis(3,4-decarboxyphenyl)hexafluoropropane dianhydride (6FDA) were determined at 298 K. The influence of the chemical structures on the physical and gas permeation properties of the 6FDA-based polyimides was studied. The solubility of propylene in an unrelaxed volume of a polymer matrix mainly contributes to the total solubility of propylene for various 6FDA-based polyimides. The diffusivity, the permeability of propylene, and the permselectivity in the propylene/propane mixed-gas system depend on the solubility of propylene. This is thought to be associated with the penetrant-induced plasticization effect. 6FDA-based polyimides, which have a high glass-transition temperature and a large fractional free volume, exhibit a high permeability with a relatively low permselectivity. Changing the number of -CH3 substituents in the phenylene linkage and changing the connectivity in the main chain are good ways of controlling the solubility of propylene and the corresponding permselectivity in the propylene/propane mixed-gas system. Some 6FDA-based polyimides restrict the solubility of propylene through the introduction of a -CONH- linkage between the phenylene linkage; the -Cl substituent in the phenylene linkage at the diamine moiety exhibits a high separation performance in the mixed-gas system. The polyimides are potentially useful membrane materials for the separation of propylene and propane in the petrochemical industry.