Issue 37, 2017

Tightening polybenzimidazole (PBI) nanostructure via chemical cross-linking for membrane H2/CO2 separation

Abstract

Membranes that permeate H2 and reject CO2 at temperatures above 150 °C are of great interest for low-cost H2 purification and pre-combustion CO2 capture. One of the leading polymers for this separation is poly[2,2′-(m-phenylene)-5,5′-bisbenzimidazole] (PBI), which has good thermal stability and high H2/CO2 selectivity. This study, for the first time, demonstrates that H2/CO2 selectivity can be significantly enhanced by chemical cross-linking of PBI in solid state, in distinct contrast with the literature where cross-linking PBI in solutions decreased H2/CO2 selectivity. We prepared a series of cross-linked PBIs by immersing PBI thin films in terephthaloyl chloride solutions for varying times to achieve different degrees of cross-linking, and then systematically investigated the effect of cross-linking on physical properties including gel content, thermal stability, cross-linking density, fractional free volume (FFV) and inter-chain spacing. Gas sorption and pure- and mixed-gas permeation properties were determined at temperatures ranging from 35 to 200 °C. Cross-linking decreased CO2 sorption and significantly increased H2/CO2 selectivity with a slight decrease in H2 permeability. For example, after cross-linking of PBI, the H2/CO2 selectivity increased from 15 to 23 while the H2 permeability decreased from 45 to 39 Barrers at 200 °C. The performance of this cross-linked PBI surpasses the Robeson's upper bound estimated at 200 °C, indicating its promise for H2 purification and CO2 capture.

Graphical abstract: Tightening polybenzimidazole (PBI) nanostructure via chemical cross-linking for membrane H2/CO2 separation

Supplementary files

Article information

Article type
Paper
Submitted
04 May 2017
Accepted
04 Sep 2017
First published
05 Sep 2017

J. Mater. Chem. A, 2017,5, 19914-19923

Tightening polybenzimidazole (PBI) nanostructure via chemical cross-linking for membrane H2/CO2 separation

L. Zhu, M. T. Swihart and H. Lin, J. Mater. Chem. A, 2017, 5, 19914 DOI: 10.1039/C7TA03874G

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