Carbon–Carbon Composite Membranes Derived from Small-Molecule-Compatibilized Immiscible PBI/6FDA-DAM-DABA Polymer Blends

Author:

Karunaweera Chamaal1,Panapitiya Nimanka P.1,Panangala Samitha1,Perez Edson V.1ORCID,Musselman Inga H.1,Balkus Kenneth J.1,Ferraris John P.1ORCID

Affiliation:

1. Department of Chemistry and Biochemistry, The University of Texas at Dallas, 800 W. Campbell Rd, Richardson, TX 75080, USA

Abstract

The use of immiscible polymer blends in gas separations is limited due to uncontrollable phase separation. In contrast, compatibilized immiscible polymer blends can be used as precursors with controlled morphologies that allow for a unique pore architecture. Herein, an immiscible polymer blend (1:1) comprising polybenzimidazole (PBI) and the copolyimide 6FDA-DAM:DABA [3:2], derived from reacting 4,4-(hexafluoroisopropylidene)diphthalic anhydride (6FDA) with 2,4,6-trimethyl-1,3-phenylenediamine (DAM) and 3,5-diaminobenzoic acid (DABA), were combined with durene diamine as a compatibilizer. The compatibilizer helped reduce the 6FDD domain sizes from 5.6 µm down to 0.77 µm and induced a more even 6FDA distribution and the formation of continuous thin-selective PBI layers. The carbon–carbon composite membranes derived from the compatibilized immiscible polymer blends showed a 3-fold increase in both H2 permeability and H2/CO2 selectivity compared to the membranes derived from non-compatibilized polymer blends. The H2 permeability of the compatibilized immiscible polymer blends increased from 3.6 to 27 Barrer, and their H2/CO2 selectivity increased from 7.2 to 20. The graphitic domain size of the carbon–carbon composite membranes derived from the polymer blends also increased from 6.3 nm for the non-compatibilized blend to 10.0 nm for the compatibilized blend.

Funder

National Science Foundation

Publisher

MDPI AG

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