4.6 Article

Selective Gas Permeation in Mixed Matrix Membranes Accelerated by Hollow Ionic Covalent Organic Polymers

期刊

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
卷 7, 期 1, 页码 1564-1573

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.8b05333

关键词

CO2 capture; Mixed matrix membrane; Polysulfone; Hollow structure; Ionic covalent organic filler

资金

  1. National University of Singapore (CENGas) [R-261-508-001-646]
  2. Ministry of Education - Singapore (MOE AcRF Tier 1) [R-279-000-472-112, R-279-000-540-114]
  3. Agency for Science, Technology and Research [PSF 1521200078, IRG A1783c0015, IAF-PP A1789a0024]

向作者/读者索取更多资源

Mixed matrix membranes (MMMs) have gained great attention for the efficient CO, removal from raw nature gas or biogas (CO2/CH4 separation) and flue gas (CO2/N-2 separation). Nevertheless, the development of high-performance MMMs for industrial applications is largely limited by the lack of suitable porous fillers. Herein, a novel ionic covalent organic polymer (ICOP-1) consisting of gas selective pores and hollow cavities is facilely fabricated using a metal triflate catalyzed condensation reaction. Considering its unique structural properties, ICOP-1 is explored as a novel filler to enhance the gas separation properties of polysulfone (PSf) membranes. Defect-free MMMs are successfully prepared owing to the high polymer-filler affinity originating from the organic nature of these two phases. Besides, the large cavities and size-selective pores of ICOP-1 lead to a simultaneous increase in membrane CO2 permeability and CO2/CH4, CO2/N-2 selectivities. With the addition of only 0.5 wt % of ICOP-1 fillers, the as-prepared MMM demonstrates the optimal gas separation performance with a CO2/CH4 selectivity of 39.7 (at a CO2 permeability of 6.19 Barrer) and a CO2/N-2 selectivity of 36.7 (at a CO2 permeability of 6.85 Barrer), opening new opportunities in membrane-based industrial CO2 capture applications.

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