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Enhancing the Gas Separation Selectivity of Mixed-Matrix Membranes Using a Dual-Interfacial Engineering Approach.

Chunhui WuKexin ZhangHongliang WangYaqi FanSongwei ZhangSanfeng HeFang WangYu TaoXiaowen ZhaoYue-Biao ZhangYan-Hang MaYongjin LeeTao Li
Published in: Journal of the American Chemical Society (2020)
We report a dual-interfacial engineering approach that uses a sub-20 nm polycrystalline MOF-74 shell as a transition phase to engineer the MOF-polymer interface. The application of a shell MOF layer divides the original single interface problem into two interfaces: MOF-MOF and MOF-polymer, which can be individually addressed. The greater external surface area created by the uneven MOF-74 shell containing high-density open metal sites allows the MOF to interact with 300% polymer at the interface compared to traditional MOF, thereby ensuring good interfacial compatibility. When applied on UiO-66-NH2, its respective mixed-matrix membranes exhibit a simultaneous increase of CO2/CH4 separation selectivity and CO2 permeability with increasing MOF loading, implying a defect-free interface. When applied on MOF-801, the mixed-matrix membranes exhibit an ethylene/ethane separation selectivity up to 5.91, a drastic 76% increase compared to that of the neat polymer owing to a "gas focusing" mechanism promoted by the preferred pore orientation in the MOF-74 layer. This represents one of the most selective ethylene/ethane separation membranes reported to date.
Keyphrases
  • metal organic framework
  • high density
  • room temperature
  • liquid chromatography
  • ionic liquid
  • molecular dynamics simulations
  • mass spectrometry
  • photodynamic therapy
  • structural basis