巴勒
膜
渗透
聚合物
选择性
吸附
化学工程
合成膜
促进扩散
磁导率
吡啶
离子键合
离子液体
材料科学
多孔性
化学
高分子化学
基质(化学分析)
色谱法
有机化学
离子
生物化学
工程类
催化作用
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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