Benchmark CO2 separation achieved by highly fluorinated nanoporous molecular sieve membranes from nonporous precursor via in situ cross-linking

Molecular sieve membranes with rigid micropores and CO2-philic functionalities within the architectures are promising candidates in CO2 separation. However, the development of effective approaches for their fabrication still remains a significant challenge. Herein, an in situ cross-linking strategy is developed for the preparation of nanoporous fluorinated molecular sieve membranes using commercially available dense and non-porous polystyrene (MPS) as a precursor template. Based on the dehydrative Friedel-Crafts reactions with highly fluorinated benzylic alcohols, MPS membranes are cross-linked in situ upon exposure to Bronsted acid (CF3SO3H), affording fluorinated microporous polymeric membranes with surface areas up to 523 m(2) g(-1) and the presence of micropores centered at 1.1-1.3 nm as well as ultra-micropores (-0.6 nm). The obtained modified membranes exhibit good ideal CO2 permeability of 797 barrer and CO2/N-2 selectivity of 28.5. In addition, high fluorine content (up to 28.5 wt%) and good thermal stability made the cross-linked membranes promising candidates to produce fluorinated carbon molecular sieve membranes with improved textural properties, exhibiting surface areas up to 1020 m(2) g(-1) and ultra-micropores of -0.4 nm. These membranes achieve superior CO2/N-2 separation performances exceeding the Robeson upper bound limit (2008).

Automated summary

This study successfully developed an in situ cross-linking strategy to prepare molecular sieve membranes with fluorinated micropores using polystyrene as a precursor template, which exhibit excellent performance in CO2/N-2 separation.