Synthesis and gas transport properties of polynaphthoylenebenzimidazoles with keto- and sulfonic bridging groups

Abstract

Polynaphthoylenebenzimidazoles (PNBI) with keto-(PNBI-CO) and sulfonic (PNBI-SO2) bridge groups were obtained by solid-state polycyclization of polyaminoimides (PANI) synthesized by polycondensation of 1,4,5,8-naphthalenetetracarboxylic acid dianhydride with 3,3`,4,4`-tetraaminobenzophenone and 3,3`,4,4`-tetraaminodiphenylsulfone in N-methylpyrrolidone, respectively. The polycondensation process and resulting chemical structure of PANI and PNBI were controlled by 1H NMR, 13C NMR and IR spectroscopy. It is shown that the temperature of solid-state polycyclization change makes it possible to obtain polymers of several of cyclization degrees. The experimental values of the gas permeability and diffusion coefficients for He, H2, N2, O2, CO2, CH4 were obtained. The gas solubility coefficients and the ideal selectivity for various gas pairs were calculated. It has been established that, in terms of the permeability-selectivity ratio, completely cyclized PNBIs occupy a more favorable position compared to incompletely cyclized ones. This result is important for polymer and a method selection to develop a selective layer of new composite membranes. The gas transport characteristics achieved for competely cyclized PNBI-SO2, as well as the film-forming properties, along with the very high thermal stability of polymers of this polymer class, are interest of further expanding the range of PNBI obtained, as well as the prospects for such new polymers using of in various gas separation processes.