Direct reforming catalyst for molten carbonate fuel cells, method for preparing the same and method for improving long-term stability thereof by wettability control on molten carbonate electrolyte
US-2016006040-A1 · Jan 7, 2016 · US
US11600836B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11600836-B2 |
| Application number | US-202117230104-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 14, 2021 |
| Priority date | Apr 11, 2016 |
| Publication date | Mar 7, 2023 |
| Grant date | Mar 7, 2023 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Disclosed here is a supported catalyst comprising a thermally stable core, wherein the thermally stable core comprises a metal oxide support and nickel disposed in the metal oxide support, wherein the metal oxide support comprises at least one base metal oxide and at least one transition metal oxide or rare earth metal oxide mixed with or dispersed in the base metal oxide. Optionally the supported catalyst can further comprise an electrolyte removing layer coating the thermally stable core and/or an electrolyte repelling layer coating the electrolyte removing layer, wherein the electrolyte removing layer comprises at least one metal oxide, and wherein the electrolyte repelling layer comprises at least one of graphite, metal carbide and metal nitride. Also disclosed is a molten carbonate fuel cell comprising the supported catalyst as a direct internal reforming catalyst.
Opening claim text (preview).
What is claimed is: 1. A supported catalyst comprising: a thermally stable core comprising a metal oxide support and nickel disposed in the metal oxide support, wherein the metal oxide support comprises at least one base metal oxide and at least one transition metal oxide or rare earth metal oxide mixed with or dispersed in the base metal oxide; an electrolyte repelling layer; and an electrolyte removing layer; wherein the electrolyte repelling layer coats the electrolyte removing layer, the electrolyte removing layer coats the thermally stable core to form a core-shell structure and comprises at least one metal oxide, and the electrolyte repelling layer comprises at least one material selected from the group consisting of graphite, metal carbide, and metal nitride. 2. The supported catalyst of claim 1 , wherein the metal oxide support has a surface area within a range of 5 to 120 m 2 /g. 3. The supported catalyst of claim 1 , wherein the base metal oxide comprises at least one alkaline metal oxide or post-transition metal oxide. 4. The supported catalyst of claim 1 , wherein the base metal oxide comprises at least one material selected from the group consisting of alumina, CaO, and MgO. 5. The supported catalyst of claim 1 , wherein the metal oxide support comprises at least two different metal oxides selected from the group consisting of transition metal oxides, rare earth metal oxides, and combinations thereof, in addition to the base metal oxide. 6. The supported catalyst of claim 5 , wherein the at least two different metal oxides selected from the group consisting of transition metal oxides, rare earth metal oxides, and combinations thereof, account for about 1-20 wt. % of the thermally stable core. 7. The supported catalyst of claim 5 , wherein the at least two different metal oxides selected from the group consisting of transition metal oxides, rare earth metal oxides, and combinations thereof, account for about 1-20 wt. % of the supported catalyst. 8. The supported catalyst of claim 1 , wherein an amount of the nickel is within a range of 10 to 50 wt. % of the supported catalyst. 9. The supported catalyst of claim 1 , wherein the supported catalyst has a mean pore diameter within a range of 65 to 700 angstroms, as measured by mercury porosimetry of pelletized catalyst, and has a pore size distribution characterized by a standard deviation of less than 10% of the mean pore diameter. 10. The supported catalyst of claim 1 , wherein the electrolyte removing layer comprises aluminum oxide, titanium oxide, zirconium oxide, tungsten oxide, a doped oxide thereof, or a mixture thereof. 11. The supported catalyst of claim 1 , wherein the electrolyte removing layer has a surface area of at least about 50 m 2 /g. 12. The supported catalyst of claim 1 , wherein the supported catalyst is free of silicate. 13. The supported catalyst of claim 1 , wherein the electrolyte removing layer comprises at least two different metal oxides. 14. The supported catalyst of claim 1 , wherein the metal oxide support comprises alumina, a zirconium oxide, and a lanthanum oxide. 15. The supported catalyst of claim 14 , wherein the supported catalyst has a mean pore diameter of about 300 angstroms, as measured by mercury porosimetry of pelletized catalyst, and has a pore size distribution characterized by a standard deviation of about 40% of the mean pore diameter. 16. A molten carbonate fuel cell comprising the supported catalyst of claim 1 as a direct internal reforming catalyst. 17. The molten carbonate fuel cell of claim 16 , wherein the direct internal reforming catalyst retains at least about 50% of its initial catalytic activity after 500 hours of operation. 18. The molten carbonate fuel cell of claim 16 , wherein the direct internal reforming catalyst retains at least about 50% of its initial catalytic activity after 700 hours of operation. 19. A method of synthesizing the supported catalyst of claim 1 , the method comprising: co-precipitating nickel with at least one base metal oxide and at least one transition metal oxide or rare earth metal oxide to form a thermally stable core; coating the thermally stable core with an electrolyte removing layer to form a core-shell structure; and coating the electrolyte removing layer with an electrolyte repelling layer, wherein the resulting synthesized supported catalyst is the supported catalyst of claim 1 .
using catalysts, e.g. selective catalysts · CPC title
Alumina · CPC title
Catalytic material supported on carriers, e.g. powder carriers (H01M4/8807, H01M4/881, H01M4/8814, H01M4/925 take precedence) · CPC title
Fuel cells · CPC title
with rare earths or actinides · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.