4.8 Article

Constructing Strong Interfacial Interactions under Mild Conditions in MOF-Incorporated Mixed Matrix Membranes for Gas Separation

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 2, 页码 3166-3174

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c19554

关键词

metal-organic framework (MOF); mixed matrix membranes; gas separation; mild condition; strong interfacial interaction; membrane stability

资金

  1. National Natural Science Funds for Distinguished Young Scholar [51625306]
  2. National Natural Science Foundation of China [51803145, 21988102]
  3. China Postdoctoral Science Foundation [2018M630598]
  4. State Key Laboratory of Separation Membranes and Membrane Processes (Tianjin Polytechnic University) [M1-201801]

向作者/读者索取更多资源

A study introduced an efficient and less destructive method to cross-link MOFs/PI mixed matrix membranes, significantly improving membrane stability and mechanical strength under relatively mild conditions without destroying membrane structure. The resulting cross-linked membranes showed significantly enhanced CO2 antiplasticization pressure and gas permeability, while also improving gas separation performance.
Although mixed matrix membranes (MMM) possess remarkably improved gas separation performance compared to traditional polymeric membranes, membrane stability including CO2 plasticization and aging is still a serious issue due to the existence of interfacial defects. In this work, we report an efficient and less destructive route to cross-link the MOFs/polyimide (PI) MMM, where amine group-functionalized MOF (NH2-UiO-66) nanoparticles are thermally cross-linked with a carboxylic acid-functionalized PI (COOH-PI) matrix to form an amide bond at the interface at 150 degrees C under vacuum condition. Such a chemical cross-linking strategy conducted at a relatively mild condition improves membrane stability greatly while ensuring that the membrane structure is not destroyed. The resulting cross-linked MMM achieves enhanced mechanical strength with higher Young's modulus than a pristine polymer membrane. The CO2 antiplasticization pressure of the MMM after cross-linking is enhanced by 200% from similar to 10 to >30 bar and the CO2 permeability of MMM only drops slightly from 995 to 735 Barrer after 450 days. At the same time, the separation performance of H-2/CH4 gas pair surpasses the 2008 upper bound and that of CO2/CH4 gas pair nearly approaches the 2008 upper bound. The cross-linking strategy used herein provides a feasible and effective route for improving membrane stability and membrane performance in the MMM system for gas separation.

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