沸石咪唑盐骨架
膜
材料科学
微型多孔材料
金属有机骨架
聚合物
化学工程
气体分离
丁烷
渗透
碳氢化合物
选择性
咪唑酯
多孔性
沸石
吸附
纳米技术
有机化学
化学
复合材料
渗透
催化作用
生物化学
工程类
作者
Ning Li,Chao Ma,Jingli Zhang,Lin Xu,Sa Wang,Ziyue Wang,Si Zhang,Jiandong Pang,Jingwei Hou,Zhihua Qiao,Chongli Zhong
标识
DOI:10.1002/anie.202506117
摘要
The integration of metal‐organic frameworks (MOFs) with polymers for efficient C4 hydrocarbon separation membranes remains challenging, primarily due to inherent phase incompatibility. This work presents an in‐situ synthesis strategy for polymer‐zeolitic‐imidazolate frameworks (polyZIF), utilizing polymer‐metal‐ligand coordination bonds combined with structural directing agents to produce crystalline microporous frameworks. With an accessible BET surface area of 261 m2/g and a permanent porosity (ca. 4.42 Å), polyZIF membrane demonstrates butadiene permeance (~332 GPU) and the selectivity over n‐butene, n‐butane, iso‐butene, and iso‐butane (17.2, 28.1, 21.5, and 34.8) under mixed gas conditions, respectively. By enhancing dispersibility and minimizing interfacial defects, polyZIFs enables the scalable fabrication of large‐area membranes (up to 80 cm2) while maintaining robust C4 separation performance. This advancement not only establishes a novel preparation for constructing polyZIF membranes with C4 hydrocarbon molecular‐sieving capability but also provides critical insights into industrial application of ZIF‐based polymer membranes.
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