Microporous polymers with cascaded cavities for controlled transport of small gas molecules.

In membrane-based separation, molecular size differences relative to membrane pore sizes govern mass flux and separation efficiency. In applications requiring complex molecular differentiation, such as in natural gas processing, cascaded pore size distributions in membranes allow different permeate molecules to be separated without a reduction in throughput. Here, we report the decoration of microporous polymer membrane surfaces with molecular fluorine. Molecular fluorine penetrates through the microporous interface and reacts with rigid polymeric backbones, resulting in membrane micropores with multimodal pore size distributions. The fluorine acts as angstrom-scale apertures that can be controlled for molecular transport. We achieved a highly effective gas separation performance in several industrially relevant hollow-fibrous modular platform with stable responses over 1 year.

Thermally rearranged (TR) bismaleimide-based network polymers for gas separation membranes.

Highly permeable, thermally rearranged polymer membranes based on bismaleimide derivatives that exhibit excellent CO2 permeability up to 5440 Barrer with a high BET surface area (1130 m2 g-1) are reported for the first time. In addition, the membranes can be easily used to form semi-interpenetrating networks with other polymers endowing them with superior gas transport properties.

Soluble, microporous, Tröger's Base copolyimides with tunable membrane performance for gas separation.

A facile two-step synthesis beginning with commercial monomers to prepare copolyimides by Tröger's Base (TB) formation provides membranes for the first time with tunable gas transport relative to hydrogen separations, CO2 plasticization resistance, and good mechanical and thermal properties.

Rational molecular design of PEOlated ladder-structured polysilsesquioxane membranes for high performance CO2 removal.

Poly(methoxy(polyethyleneoxy)propyl-co-methacryloxypropyl) silsesquioxane membranes with different copolymer ratios were successfully fabricated via UV-induced crosslinking with mechanical stability. By selectively introducing polyethylene oxide (PEO) groups covalently bound to the ladder-structured polysilsesquioxane, we effectively suppressed the PEO crystallization, allowing for excellent CO2/H2 and CO2/N2 separation under single as well as mixed gas conditions.