材料科学
膜
聚合物
化学工程
单体
微型多孔材料
聚酰亚胺
高分子化学
多孔性
气体分离
原位聚合
互连性
聚合
界面聚合
纳米技术
复合材料
化学
图层(电子)
生物化学
人工智能
计算机科学
工程类
作者
Maria F. Jimenez‐Solomon,Qilei Song,Kim E. Jelfs,Marta Munoz-Ibanez,Andrew G. Livingston
出处
期刊:Nature Materials
[Springer Nature]
日期:2016-05-02
卷期号:15 (7): 760-767
被引量:670
摘要
Highly permeable and selective membranes are desirable for energy-efficient gas and liquid separations. Microporous organic polymers have attracted significant attention in this respect owing to their high porosity, permeability and molecular selectivity. However, it remains challenging to fabricate selective polymer membranes with controlled microporosity that are stable in solvents. Here we report a new approach to designing crosslinked, rigid polymer nanofilms with enhanced microporosity by manipulating the molecular structure. Ultrathin polyarylate nanofilms with thickness down to 20 nm are formed in situ by interfacial polymerization. Enhanced microporosity and higher interconnectivity of intermolecular network voids, as rationalized by molecular simulations, are achieved by using contorted monomers for the interfacial polymerization. Composite membranes comprising polyarylate nanofilms with enhanced microporosity fabricated in situ on crosslinked polyimide ultrafiltration membranes show outstanding separation performance in organic solvents, with up to two orders of magnitude higher solvent permeance than membranes fabricated with nanofilms made from non-contorted planar monomers.
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