Abstract
Polymeric membranes with metal-organic frameworks (MOFs) holds great potential for gas separation. However, finely tailoring the adhesion between MOFs and polymer matrices is crucial in reducing the membranes defective structure. The partial inorganic structure of MOFs limits the interaction with the polymer matrix, which tends to agglomerate on the membranes. Herein, an interfacial strategy is reported by post-synthetic functionalization of MIL-53 (Al) with ionic liquids (ILs) to construct IL@MIL-53 (Al) composite to improve interfacial interaction among filler and polysulfone (PSf) matrices. At 2 wt% of IL@MIL-53 (Al), the composite membranes tensile strength and % elongation were enhanced by about 66.13 and 97.40% compared to the neat PSf membrane. The intimate contact between IL@MIL-53 (Al) and PSf matrices renders uniform dispersion evident from morphological studies. The gas permeation properties were evaluated for carbondioxide (CO2), nitrogen (N2), methane (CH4) gases. At 2 wt% of MIIL-53 (Al) nanofiller, the CO2 permeance was found to be 37.56 ± 0.63 GPU which was significantly higher than the neat PSf membrane. Besides, the CO2 permeance of the PSf/2% IL@MIL-53 (Al) membrane was noted to be 34.23 ± 0.68 GPU, whereas the CO2/CH4 and CO2/N2 selectivities were 48.64 and 49.19% higher than the neat membrane. As the pressure increased from 2 to 10 bar, the CO2, N2, and CH4 gas permeances in composite PSf membranes were decreased, whereas the CO2/N2 and CO2/CH4 selectivities were observed to be increased. The introduction of ILs into the MOFs pores will tune pore size with the enhanced adsorption selectivity due to its high CO2 solubility and affinity of ILs. ILs functionalization on the cores of the MIL-53 (Al) structure is an effective strategy, which opens up the selection to a broad range of fillers in the aspect of commercialization.
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