Relationships between chemical structures and solubility, diffusivity, and permselectivity of 1,3‐butadiene and n‐butane in 6FDA‐based polyimides

Abstract

The solubility, diffusivity, and permselectivity of 1,3-butadiene and n-butane in seven different polyimides synthesized from 2,2-bis (3,4-carboxyphenyl) hexafluoropropane dianhydride (6FDA) were determined at 298 K. The influence of chemical structures on physical and gas permeation properties of 6FDA-based polyimides was studied. Solubility of 1,3-butadiene in 6FDA-based polyimides can be described by a dual-mode sorption model. 1,3-Butadiene-induced plasticization is considered to be associated with the increasing permeabilities of 1,3-butadiene and n-butane and the decreasing permselectivity of 1,3-butadiene vs. n-butane in the mixed gas system containing a high concentration of 1,3-butadiene. It was found that controlling the solubility of 1,3-butadiene in an unrelaxed volume in 6FDA-based polyimides is very important to maintain the high permselectivity of 1,3-butadiene vs. n-butane in the mixed gas system. Changing the C(CF3)2 linkage to a CH2, O linkage, removing methyl substituents at the ortho position of the imide linkage, and changing the p-phenylene linkage to an m-phenylene linkage in the main chains in some 6FDA-based polyimides are effective to decrease fractional free volume and restrict the solubility of 1,3-butadiene in the unrelaxed volume of a polymer matrix. The 6FDA-based polyimides restricting the solubility of 1,3-butadiene in an unrelaxed volume exhibit high separation performance in the 1,3-butadiene/n-butane mixed gas system compared with conventional glassy polymers and, therefore, are potentially useful membrane materials for the separation of 1,3-butadiene and n-butane in the petrochemical industry. © 1999 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 37: 2941–2949, 1999