磁导率
气体分离
多孔性
化学
渗透
相位反转
基质(化学分析)
作者
Chenhui Wang,Fangyuan Guo,He Li,Jian Xu,Jun Hu,Honglai Liu,Meihong Wang
标识
DOI:10.1016/j.memsci.2019.117677
摘要
Abstract Inspired by the most efficient CO2 transport across natural biological membranes, a novel bionic channel facilitating CO2 permeation was realized via adding a filtering porous ionic polymer (PIP) in a mixed matrix membrane (MMM). A series of polymer of intrinsic microporosity (PIM-1) based MMMs were fabricated by three pyridine-based PIPs (PIP-Py-X) with different Cl−, Ac−, and BF4− anions as fillers. PIP-Py-X PIPs show highly selective CO2 adsorption capacity and perfect interfacial compatibility with the PIM-1 matrix. More significantly, acting as carriers, the movable anions in the MMMs efficiently facilitated the transport of adsorbed CO2 across the membranes. As a result, the obtained PIM-Py-Ac-15 MMM exhibited an excellent permeability for CO2 of 6205 barrer and a CO2/N2 and CO2/CH4 selectivity of 62.5 and 56.1, respectively, far surpassing the 2008 Robeson upper bound and exceeding most of the reported advanced membranes. As a divertive of PIPs, this work opens a window for designing and fabricating promising MMMs for task-specific membrane separations.
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