Selective CO Methanation on Highly Active Ru/TiO2 Catalysts: Identifying the Physical Origin of the Observed Activation/Deactivation and Loss in Selectivity-Reference-Cited by-同舟云学术

Selective CO Methanation on Highly Active Ru/TiO2 Catalysts: Identifying the Physical Origin of the Observed Activation/Deactivation and Loss in Selectivity

Published:2018-04-27 Issue:6 Volume:8 Page:5399-5414
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Abdel-Mageed Ali M.¹,Widmann Daniel¹,Olesen Sine E.²,Chorkendorff Ib²^ORCID,Behm R. Jürgen¹^ORCID

Affiliation:

1. Institute of Surface Chemistry and Catalysis, Ulm University, D-89069 Ulm, Germany

2. Department of Physics, Technical University of Denmark, DK-2800 Lyngby, Denmark

Funder

Villum Fonden

Publisher

American Chemical Society (ACS)

Subject

Catalysis,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acscatal.8b00384

Reference68 articles.

1. High Catalytic Performance of Ruthenium-Doped Mesoporous Nickel-Aluminum Oxides for Selective CO Methanation

2. Performance evaluation and comparison of fuel processors integrated with PEM fuel cell based on steam or autothermal reforming and on CO preferential oxidation or selective methanation

3. Complete removal of carbon monoxide in hydrogen-rich gas stream through methanation over supported metal catalysts

4. Selective methanation of CO over supported noble metal catalysts: Effects of the nature of the metallic phase on catalytic performance

5. What drives the selectivity for CO methanation in the methanation of CO2-rich reformate gases on supported Ru catalysts?

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