Effect of structure and conformational composition on the transport behavior of poly(ether imides)

Abstract

With the example of two isostructural poly(ether imides), the effects of isopropylidene and hexafluoroisopropylidene groups and hydrogen bonding with chloroform on changes in geometry and energy parameters of polymer chains have been analyzed. The relationship between changes in the geometry characteristics of polymer chains and the gas-separation behavior of films cast from these poly(ether imides) has been established. It has been shown that an increase in permeability is related to a rise in rotation barriers and, consequently, to enhancement of chain rigidity, while the improvement of gas-separation selectivity is associated with a reduction in the amount of isoenergy conformers and an increase in the conformational uniformity of polymer chains. As was detected by FTIR spectroscopy and confirmed by quantum-chemical calculations, the conformational nonuniformity and the small-scale mobility of poly(ether imide) chains are possible only in the Ph-O-Ph′ fragment. The data obtained are applicable for estimation of the role of molecular mobility of polymer chains in the mechanism of gas or penetrant transfer through the polymer film and for predicting the transport behavior of polymers from this family. With the example of two other poly(ether imides), the prediction is confirmed by the experimental data on gas separation.