Rational macromolecular design and strategies to tune the microporosity for high-performance O2/N2 separation membranes

被引:6
|
作者
Liu, Ying [1 ]
Chen, Xiaobo [1 ]
Han, Tianliang [1 ]
Wang, Can [1 ]
Liu, Hongyan [1 ]
Sun, Ying [1 ]
Zheng, Peijun [1 ]
Zhang, Haitao [1 ]
Luo, Shuangjiang [1 ]
机构
[1] Chinese Acad Sci, Beijing Key Lab Ion Liquids Clean Proc, State Key Lab Multiphase Complex Syst, CAS Key Lab Green Proc & Engn,Inst Proc Engn, Beijing 100190, Peoples R China
关键词
Gas separation membrane; Pore structure regulation; O2/N2; separation; Microporosity; Polymers of intrinsic microporosity; Physical aging; MOLECULAR-SIEVE MEMBRANES; GAS PERMEATION PROPERTIES; INCORPORATING TROGERS BASE; OXYGEN-ENRICHED AIR; INTRINSIC MICROPOROSITY; LADDER POLYMERS; TRANSPORT PROPERTIES; FREE-VOLUME; POLYIMIDE MEMBRANES; LINKED POLYMER;
D O I
10.1016/j.seppur.2023.125978
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
This review summarizes the performance of recently developed microporous polymers for practical industrial O2/N2 separations. The macromolecular design of innovative polymers of intrinsic porosity and derivatives is evaluated from the perspective of pore structure regulation for their outstanding O2/N2 separation performance. The structural groups that could fine-tune the free volume elements are examined to discern the promising moiety and architectures to improve size-based sieving. The long-term aging behaviors of the state-of-the-art macromolecules are also screened to explore the impacts of improved pore/free volume configuration. The strategies using thermal treatments to reset the structure of microporosity are inspected for their potential to improve the gas permeability or enhance size-specific molecular sieving, including the thermal rearrangement of polymeric membranes and pyrolyzed carbon molecular membranes using pre-crosslinked precursors and PIMderived precursors. Membrane process design and optimization are summarized to evaluate the prospects of these novel membrane materials for large-scale industrial applications.
引用
收藏
页数:20
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