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Triptycene-containing polyimide membranes with tunable fractional free volume promoting fast gas transport and selective separations.

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This paper reports a new macromolecular design that incorporates hierarchical triptycene unit into thermally rearranged polybenzoxazole (TR-PBO) structures for highly selective and permeable gas separation membranes with great potential for H 2 purification and CO 2 removal from natural gas. We demonstrate that triptycene moieties not only effectively disrupt chain packing enabling microporous structure for fast mass transport, but also introduce ultrafine microporosity via the unique internal free volume intrinsic to triptycene unit that allows for superior molecular sieving capability in resulting PBO membranes. Consequently, these triptycene-based polybenzoxazole (TPBO) membranes display among the highest gas selectivities for H 2 separations (i.e., α(H 2 /N 2 ) = 96; α(H 2 /CH 4 ) = 203) and CO 2 removal from natural gas (i.e., α(CO 2 /CH 4 ) = 68) among existing glassy polymeric membranes. It is also demonstrated that microporous structure and gas transport properties of TPBO films are highly tailorable by adjusting the triptycene content and the ortho-functionality of the precursors. The highly diverse tunability, along with the excellent resistance toward membrane plasticization and physical aging, render the TPBO membranes with extremely versatile separation capability applicable for a wide range of important industrial processes to get clean or low carbon fuels and reduce carbon footprint.

Poly(ethylene oxide) (PEO)-containing polymer membranes are attractive for CO2-related gas separations due to their high selectivity toward CO2. However, the development of PEO-rich membranes is frequently challenged by weak mechanical properties and a high crystallization tendency of PEO that hinders gas transport. Here we report a new series of highly CO2-selective, amorphous PEO-containing segmented copolymers prepared from commercial Jeffamine polyetheramines and pentiptycene-based polyimide. The copolymers are much more mechanically robust than the nonpentiptycene containing counterparts due to the molecular reinforcement mechanism of supramolecular chain threading and interlocking interactions induced by the pentiptycene structures, which also effectively suppresses PEO crystallization leading to a completely amorphous structure even at 60% PEO weight content. Membrane transport properties are sensitively affected by both PEO weight content and PEO chain length. A nonlinear correlation between CO2 permeability with PEO weight content was observed due to the competition between solubility and diffusivity contributions, whereby the copolymers change from being size-selective to solubility-selective when PEO content reaches 40%. CO2 selectivities over H2 and N2 increase monotonically with both PEO content and chain length, indicating strong CO2-philicity of the copolymers. The copolymer film with the longest PEO sequence (PEO2000) and highest PEO weight content (60%) showed a measured CO2 pure gas permeability of 39 Barrer, and ideal CO2/H2 and CO2/N2 selectivities of 4.1 and 46, respectively, at 35 °C and 3 atm, making them attractive for hydrogen purification and carbon capture.