Catalyst compositions having enhanced acidity for dry reforming processes
US-2021229074-A1 · Jul 29, 2021 · US
US12054389B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12054389-B2 |
| Application number | US-202217670606-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 14, 2022 |
| Priority date | Feb 14, 2022 |
| Publication date | Aug 6, 2024 |
| Grant date | Aug 6, 2024 |
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Catalyst compositions containing red mud and rhodium are provided. An exemplary catalyst composition includes about 50 wt % to about 99 wt % of a mixed-oxide material including iron oxide, aluminum oxide, and silicon oxide, and about 1 wt % to about 40 wt % of rhodium oxide, calculated as Rh 2 O 3 .
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What is claimed is: 1. A catalyst composition comprising: about 50 wt. % to about 90 wt. % of a mixed-oxide material comprising iron oxide, aluminum oxide, and silicon oxide; and about 10 wt % to about 40 wt % of rhodium oxide, calculated as Rh 2 O 3 , wherein a Brunauer-Emmett-Teller (BET) surface area of the catalyst composition is at least about 100 m 2 /g. 2. The catalyst composition of claim 1 , wherein the mixed-oxide material comprises: about 5 wt % to about 60 wt % of iron oxide, calculated as Fe 2 O 3 ; about 5 wt % to about 30 wt % of aluminum oxide, calculated as Al 2 O 3 ; and about 3 wt % to about 50 wt % of silicon oxide, calculated as SiO 2 . 3. The catalyst composition of claim 1 , wherein the mixed-oxide material further comprises at least one of sodium oxide, calcium oxide, and titanium oxide. 4. The catalyst composition of claim 3 , wherein the mixed-oxide material comprises: up to about 15 wt % of titanium oxide, calculated as TiO 2 ; up to about 14 wt % of calcium oxide, calculated as CaO; and up to about 10 wt % of sodium oxide, calculated as Na 2 O. 5. The catalyst composition of claim 1 , wherein the mixed-oxide material comprises: about 30 wt % to about 60 wt % of iron oxide, calculated as Fe 2 O 3 ; about 10 wt % to about 20 wt % of aluminum oxide, calculated as Al 2 O 3 ; about 3 wt % to about 50 wt % of silicon oxide, calculated as SiO 2 ; about 5 wt % to about 15 wt % of titanium oxide, calculated as TiO 2 , about 2 wt % to about 8 wt % of calcium oxide, calculated as CaO; and about 2 wt % to about 10 wt % of sodium oxide, calculated as Na 2 O. 6. The catalyst composition of claim 1 , wherein the mixed-oxide material comprises red mud from a process for extracting alumina from bauxite. 7. The catalyst composition of claim 1 , comprising about 50 wt. % to about 85 wt. % of a mixed-oxide material comprising iron oxide, aluminum oxide, and silicon oxide; and about 15 wt % to about 30 wt. % of rhodium oxide. 8. The catalyst composition of claim 1 , wherein the rhodium oxide is supported on the mixed-oxide material. 9. The catalyst composition of claim 1 , wherein a BET surface area of the catalyst composition is at least about 125 m 2 /g. 10. The catalyst composition of claim 1 , wherein a BET surface area of the catalyst composition is about 125 m 2 /g to about 200 m 2 /g. 11. A method for preparing the catalyst composition of claim 1 , the method comprising: contacting a mixed-oxide material comprising iron oxide, aluminum oxide, and silicon oxide with an acid to form an acid-treated support; precipitating a mixture of the acid-treated support and rhodium to form a precursor composition; and calcining the precursor composition to form the catalyst composition, wherein the catalyst composition comprises: about 50 wt. % to about 90 wt. % of a mixed-oxide material comprising iron oxide, aluminum oxide, and silicon oxide; and about 10 wt % to about 40 wt % of rhodium oxide, calculated as Rh 2 O 3 , and wherein a Brunauer-Emmett-Teller (BET) surface area of the catalyst composition is at least about 100 m 2 /g. 12. The method of claim 11 , wherein the mixed-oxide material comprises red mud from a process for extracting alumina from bauxite. 13. The method of claim 11 , wherein contacting the mixed-oxide material with an acid comprises adding the acid to an aqueous solution comprising the mixed-oxide material. 14. The method of claim 11 , wherein the acid comprises hydrochloric acid. 15. The method of claim 11 , wherein contacting the mixed-oxide material with acid forms an acid-treated support comprising a BET surface area of at least about 140 m 2 /g. 16. The method of claim 11 , wherein precipitating the mixture of the acid-treated support and rhodium comprises adding a base to an aqueous solution comprising the acid-treated support and a rhodium salt. 17. The method of claim 16 , wherein the base is ammonia. 18. The method of claim 16 , wherein adding the base to the aqueous solution increases the pH of the solution to greater than about 8. 19. The method of claim 16 , wherein the rhodium salt is rhodium acetylacetonate. 20. The method of claim 11 , further comprising: filtering the precursor composition; drying the filtered precursor composition; and calcining the dried precursor composition. 21. A method for dry reforming methane, the method comprising contacting methane and carbon dioxide with the catalyst composition of claim 1 comprising: about 50 wt. % to about 90 wt. % of a mixed-oxide material comprising iron oxide, aluminum oxide, and silicon oxide; and about 10 wt % to about 40 wt % of rhodium oxide, calculated as Rh 2 O 3 , wherein a Brunauer-Emmett-Teller (BET) surface area of the catalyst composition is at least about 100 m 2 /g; to form H 2 and CO. 22. The method of claim 21 , wherein the mixed-oxide material comprises red mud from a process for extracting alumina from bauxite. 23. The method of claim 21 , comprising contacting methane and carbon dioxide with the catalyst composition at a temperature of about 500° C. to about 1,000° C. 24. The method of claim 21 , comprising contacting methane and carbon dioxide with the catalyst composition at a pressure of about 5 bar to about 20 bar. 25. The method of claim 21 , comprising contacting methane and carbon dioxide with the catalyst composition at a gas hourly space velocity (GHSV) of about 1,000 h −1 to about 10,000 h −1 .
X-ray diffraction · CPC title
100-500 m2/g · CPC title
10-100 m2/g · CPC title
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the reforming step being a carbon dioxide reforming step · CPC title
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