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Zhaolin Shi1,2,3, Yu Tao1, Jiasheng Wu1

  • 1School of Physical Science and Technology , ShanghaiTech University , Shanghai 201210 , China.

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|January 24, 2020
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Chemically stable metal-organic frameworks (MOFs) with appended amino groups show high selectivity for capturing carbon dioxide (CO2) from humid flue gas. These robust MOFs offer efficient CO2 separation with low regeneration energy.

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Area of Science:

  • Materials Science
  • Chemical Engineering
  • Environmental Science

Background:

  • Developing robust metal-organic frameworks (MOFs) is crucial for effective postcombustion carbon dioxide (CO2) capture from industrial flue gases.
  • Flue gas often contains water vapor and acidic components, posing significant challenges to the stability and performance of existing CO2 sorbents.

Purpose of the Study:

  • To design and synthesize thermally and chemically stable MOFs for efficient CO2 capture under humid conditions.
  • To investigate the impact of appending amino groups to triazolate linkers on MOF stability and CO2 adsorption properties.

Main Methods:

  • Synthesis of novel MOFs with amino-functionalized triazolate linkers.
  • Characterization of MOF chemical and thermal stability against aqueous, acidic, and basic environments.
  • Gas adsorption studies to determine CO2/N2 and CO2/H2O selectivity, including thermodynamic and kinetic assessments.

Main Results:

  • The synthesized MOFs demonstrated exceptional chemical stability.
  • Achieved high thermodynamic CO2/N2 selectivity (up to 120) and kinetic CO2/H2O selectivity (up to 70).
  • Identified distinct adsorption sites for CO2 and H2O within the MOF channels.
  • The optimal MOF exhibited low regeneration energy, high CO2 capture utility in humid conditions, and good cycling stability.

Conclusions:

  • Appending amino groups to triazolate linkers is an effective strategy for enhancing MOF stability in challenging flue gas environments.
  • These amino-functionalized MOFs show promising performance for postcombustion CO2 capture, particularly under humid conditions.
  • The distinct adsorption sites contribute to the observed high selectivity for CO2 over N2 and H2O.