膜
聚合物
气体分离
分子间力
化学工程
选择性
材料科学
磁导率
高分子化学
体积热力学
化学
分子
有机化学
热力学
复合材料
催化作用
生物化学
工程类
物理
作者
Peter M. Budd,Kadhum J. Msayib,Carin E. Tattershall,Bader S. Ghanem,Kevin J. Reynolds,Neil B. McKeown,Detlev Fritsch
标识
DOI:10.1016/j.memsci.2005.01.009
摘要
When polymeric membranes are employed to remove selectively one component from a gaseous mixture, there is generally a trade-off between selectivity and permeability. Data are presented for two polymers of intrinsic microporosity, PIM-1 and PIM-7, which show a significant advance across the previous upper bound of performance for commercially important gas pairs, including O2/N2 and CO2/CH4. The exceptional properties of PIMs arise from their rigid but contorted molecular structures, which frustrate packing and so create free volume, coupled with chemical functionality giving strong intermolecular interactions.
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