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Author:

Ma, M. (Ma, M..) | Zhang, Y. (Zhang, Y..) | Gao, C. (Gao, C..) | Liu, G. (Liu, G..) | Cui, C. (Cui, C..) | Duoni (Duoni.) | Hu, Q. (Hu, Q..) | Hunaidy, A.S. (Hunaidy, A.S..) | Moniee, M.A. (Moniee, M.A..) | Dawsari, Y.A. (Dawsari, Y.A..) | Alahmed, A.H. (Alahmed, A.H..) | Qian, W. (Qian, W..)

Indexed by:

EI Scopus SCIE

Abstract:

The present work reported the space confinement effect of carbon nanotube-alumina strip (CAS) support on the Cu-Co bimetallic catalyst or the single Cu, Co catalysts for the CO2 methanation. CAS, made by extrusion of nanotubes and Al-based sol and high temperature calcination, was a macroscopic support with sufficient mesopores and hydrophobic property. Cu-Co/CAS catalysts exhibited high catalytic activity for methanation of CO2 (H2/CO2=3:1), where CO2 conversion was 49.62% and CH4 selectivity was 95.98% at temperature as low as 250 ℃ and 1.5 MPa, and showed advantage significantly over those with the supports of individual nanotube or pure Alumina support. The comparison suggested the hydrophobicity of carbon nanotubes can effectively remove water from the metal active sites, enhancing the equilibrium of reverse water gas shift and CO methanation reactions, as compared to alumina support. Additionally, CAS support had a spatial confinement effect that increased the contact time of CO2 or intermediates with the active sites, compared with individual nanotube support. XPS and Raman spectroscopy validated the presence of oxygen vacancies of CAS, promoting the CO2 methanation. H2-TPR results, in combination with DFT calculations, confirmed that the CAS supports enabled the Cu-Co active phase by changing their electronic structures, to possess a strong adsorption activation capacity for H2 at low temperatures with high performance for CO2 methanation. © 2024 Elsevier B.V.

Keyword:

Cu-Co bimetallic Spatial confinement CAS support Electronic structure Low temperature CO2 methanation

Author Community:

  • [ 1 ] [Ma M.]Department of Chemical Engineering, Tsinghua University, 100084, China
  • [ 2 ] [Zhang Y.]Department of Chemical Engineering, Tsinghua University, 100084, China
  • [ 3 ] [Gao C.]Department of Chemical Engineering, Tsinghua University, 100084, China
  • [ 4 ] [Liu G.]Department of Chemical Engineering, Tsinghua University, 100084, China
  • [ 5 ] [Liu G.]College of Environmental and Energy Engineering, Beijing University of Technology, 100124, China
  • [ 6 ] [Cui C.]Department of Chemical Engineering, Tsinghua University, 100084, China
  • [ 7 ] Duoni, Department of Chemical Engineering, Tsinghua University, 100084, China
  • [ 8 ] [Hu Q.]Research and Development Center, Dhahran, Saudi Aramco, 31311, Saudi Arabia
  • [ 9 ] [Hunaidy A.S.]Research and Development Center, Dhahran, Saudi Aramco, 31311, Saudi Arabia
  • [ 10 ] [Moniee M.A.]Research and Development Center, Dhahran, Saudi Aramco, 31311, Saudi Arabia
  • [ 11 ] [Dawsari Y.A.]Research and Development Center, Dhahran, Saudi Aramco, 31311, Saudi Arabia
  • [ 12 ] [Alahmed A.H.]Research and Development Center, Dhahran, Saudi Aramco, 31311, Saudi Arabia
  • [ 13 ] [Qian W.]Department of Chemical Engineering, Tsinghua University, 100084, China
  • [ 14 ] [Qian W.]Ordos Laboratory, Inner Mongolia, 017000, China

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Source :

Catalysis Today

ISSN: 0920-5861

Year: 2024

Volume: 437

5 . 3 0 0

JCR@2022

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count: 2

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 9

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