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Adsorption

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Investigation of CO2 capture using acetate-based ionic liquids incorporated into exceptionally porous metal–organic frameworks

  • Mohanned Mohamedali
  • Amr Henni
  • Hussameldin IbrahimEmail author
Article

Abstract

The potential advantage of using supported ionic liquids (SILs) for CO2 capture applications has been investigated in this work. The impregnation of 1-ethyl-3-methylimidazolium Acetate [emim][Ac] into two voluminous metal–organic frameworks (MOF-177 and MIL-101) is evaluated using different synthesis methods. The performance of the composite sorbents for CO2 capture has been evaluated using various characterization techniques. The successful incorporation of [emim][Ac] into the pores of MOF-177 and MIL-101 have been confirmed using thermogravimetric analysis and Fourier transform infrared spectroscopy results. Furthermore, the porosity of the as-synthesized samples using different synthesis methods have been measured using N2 adsorption experiments to evaluate the changes in the specific surface areas and pore volumes upon the introduction of [emim][Ac] to the support materials. A significant decrease in the porosity was realized for the [emim][Ac]-confined samples especially when using wet impregnation synthesis method compared to the dry mixing approach. The crystal structures of the MOF-177 and MIL-101 were found to be maintained after the synthetic steps, with some reductions in the X-ray diffraction peak intensities. No improvements in the CO2 uptakes could be achieved for the MIL-101 samples using both synthesis strategies, whereas the [emim][Ac]@MOF-177 samples prepared using wet impregnation method, has shown a remarkable enhancement in the CO2 capacity up to 0.3 mmol/g at 0.15 bar and 303 K. Moreover, the adsorption kinetics in MOF-177 based samples was found to be significantly fast as depicted from the first order rate constant values. The [emim][Ac]@MOF-177 samples exhibited a substantially stable cyclic adsorption–desorption performance up to 10 successive cycles with a considerably fast desorption kinetics.

Keywords

Metal–organic framework Ionic liquids Impregnation CO2 capture MIL-101 MOF-177 

Notes

Acknowledgements

The authors would like to acknowledge the Faculty of Graduate Studies and Research (FGSR) at the University of Regina for the financial support in the form of a Graduate Research Fellowship (GRF). Acknowledgments are also due to the Natural Sciences and Engineering Research Council of Canada (NSERC), the Canada Foundation for Innovation (CFI), and the Clean Energy Technologies Research Institute (CETRi) at the University of Regina.

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© Springer Science+Business Media, LLC, part of Springer Nature 2019

Authors and Affiliations

  1. 1.Process Systems Engineering, Faculty of Engineering and Applied ScienceClean Energy Technologies Research Institute (CETRi), University of ReginaReginaCanada

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