A new dip-coating approach for plasticization-resistant polyimide hollow fiber membranes: In situ thermal imidization and cross-linking of polyamic acid

Abstract Polymeric hollow fiber membranes (HFMs) are in high demand for gas separation due to their superior processability and cost-effectiveness, despite exhibiting high vulnerability to plasticization. However, most glassy polymeric HFMs have been prepared by a rather complicated dry-jet/wet-quench process. Herein, we demonstrate a simple dip-coating method of fabricating defect-free and plasticization-resistant polyimide HFMs on a cross-linked polyimide/polysilsesquioxane hollow fiber support via in situ thermal imidization and cross-linking of a polyamic acid (PAA) precursor solution. The use of a thermally stable cross-linked nanoporous hollow fiber support ensures the coating of various glassy PAA solutions prepared by different dianhydrides and diamine monomers without disturbing its internal pore structure. The resulting polyimide hollow fiber membranes enhanced CO2/CH4 separation performance compared to as-synthesized polyimide solution-coated counterpart. It is because in situ thermal imidization and cross-linking of PAA solutions induced the formation of more imine linkages, possibly generating larger free volume elements due to the disturbance of intersegmental chain packing while maintaining sufficient chain rigidity. Additionally, the membrane’s practical applicability was confirmed as the hollow fibers demonstrated resistance to plasticization when subjected to an equimolar CO2/CH4 mixed feed of approximately 50 bar. Our simple but versatile dip-coating approach allows for the formation of highly plasticization-resistant polyimide HFMs.