膜
选择性
气体分离
巴勒
瓶颈
化学工程
聚合物
材料科学
磁导率
膜技术
纳米技术
化学
工艺工程
有机化学
计算机科学
催化作用
工程类
复合材料
生物化学
嵌入式系统
作者
Mengxi Zhang,Xuechun Jing,Shuang Zhao,Pengpeng Shao,Yuanyuan Zhang,Shuai Yuan,Yanshuo Li,Cheng Gu,Xiaoqi Wang,Yanchun Ye,Xiao Feng,Bo Wang
标识
DOI:10.1002/anie.201904385
摘要
Membrane technologies that do not rely on heat for industrial gas separation would lower global energy cost. While polymeric, inorganic, and mixed-matrix separation membranes have been rapidly developed, the bottleneck is balancing the processability, selectivity, and permeability. Reported here is a softness adjustment of rigid networks (SARs) strategy to produce flexible, stand-alone, and molecular-sieving membranes by electropolymerization. Here, 14 membranes were rationally designed and synthesized and their gas separation ability and mechanical performance were studied. The separation performance of the membranes for H2 /CO2 , H2 /N2 , and H2 /CH4 can exceed the Robeson upper bound, among which, H2 /CO2 separation selectivity reaches 50 with 626 Barrer of H2 permeability. The long-term and chemical stability tests demonstrate their potential for industrial applications. This simple, scalable, and cost-effective strategy holds promise for the design other polymers for key energy-intensive separations.
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