Enhancing selectivity of ZIF-8 membranes by short-duration postsynthetic ligand-exchange modification

Post-synthesis modification of zeolitic imidazolate framework (ZIF) membranes offers new opportunities to tailor ZIF structures and improve their separation performance. This work utilizes membrane surface ligand exchange (MSLE) to replace methylimidazole (MeIM) with 5,6-dimethylbenzimidazole (DBIM) and investigates its effect on the gas separation properties of ZIF-8 membranes containing varying amounts of intercrystalline defects (perfect and imperfect membranes). Upon short time (0.5 h) MSLE modification, the pristine ZIF-8 membrane shows a significant enhancement in H-2/C2H6 selectivity (12-22) and C3H6/C3H8 selectivity (150-188) with small declines in gas permeance (29.5% for H-2, 6.5% for C3H6). MSLE modification also improves the separation performance of imperfect ZIF-8 membranes, but to a lesser extent (C3H6/C3H8 selectivity increasing from 37.5 to 63.3). Some of the MeIM in the ZIF-8 membrane crystals are replaced by bulkier DBIM, facilitated by the presence of the intercrystalline pores resulting in more exchange on the imperfect membrane. The short-duration ligand exchange reduces intracrystalline pore diffusivity, to a greater extent for larger molecules as compared to smaller molecules, leading to a reduction in gas permeance and an increase in separation factor. However, long- duration (5 h) MSLE modification on a perfect ZIF-8 membrane lowers the C3H6/C3H8 selectivity due to an increase in the intercrystalline transport for bulkier C3H8 with an increase in C3H6 permeance due to enhanced solubility within the modified ZIF-8 structure.

Automated summary

Post-synthesis modification of ZIF membranes through membrane surface ligand exchange (MSLE) has shown significant improvements in gas separation performance, particularly in H-2/C2H6 and C3H6/C3H8 selectivity, while the impact on C3H6/C3H8 selectivity is less pronounced.