Advances in the studies of the supported ruthenium catalysts for CO 2 methanation
Chinese Journal of Catalysis, ISSN: 1872-2067, Vol: 63, Page: 1-15
2024
- 5Citations
- 29Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Review Description
CO 2 methanation has a potential in the large-scale utilization of carbon dioxide. It has also been considered to be useful for the renewable energy storage. The commercial pipeline for natural gas transportation can be directly applied for the methane product of CO 2 methanation. The supported ruthenium (Ru) catalyst has been confirmed to be active and stable for CO 2 methanation with its high ability in the dissociation of hydrogen and the strong binding of carbon monoxide. CO 2 methanation over the supported Ru catalyst is structure sensitive. The size of the Ru catalyst and the support have significant effects on the activity and the mechanism. A significant challenge remained is the structural controllable preparation of the supported Ru catalyst toward a sufficiently high low-temperature activity. In this review, the recent progresses in the investigations of the supported Ru catalysts for CO 2 methanation are summarized. The challenges and the future developments are also discussed.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S1872206724600902; http://dx.doi.org/10.1016/s1872-2067(24)60090-2; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85201730103&origin=inward; https://linkinghub.elsevier.com/retrieve/pii/S1872206724600902; http://sciencechina.cn/gw.jsp?action=cited_outline.jsp&type=1&id=7787645&internal_id=7787645&from=elsevier; http://dx.doi.org/10.1016/s1872-2067%2824%2960090-2
Elsevier BV
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