Methods and systems for upgrading mixed pyrolysis oil to light aromatics over mixed metal oxide catalysts
US-2024010934-A1 · Jan 11, 2024 · US
US9616414B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9616414-B2 |
| Application number | US-201414273256-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 8, 2014 |
| Priority date | May 9, 2013 |
| Publication date | Apr 11, 2017 |
| Grant date | Apr 11, 2017 |
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Disclosed is a hydrocarbon gas reforming supported catalyst, and methods for its use, that includes a catalytic material capable of catalyzing the production of a gaseous mixture comprising hydrogen and carbon monoxide from a hydrocarbon gas, and a support material comprising an alkaline earth metal/metal oxide compound having a structure of D-E, wherein D is a M 1 or M 1 M 2 , M 1 and M 2 each individually being an alkaline earth metal selected from the group consisting of Mg, Ca, Ba, and Sr, E is a metal oxide selected from the group consisting of Al 2 O 4 , SiO 2 , ZrO 2 , TiO 2 , and CeO 2 , wherein the catalytic material is attached to the support material.
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The invention claimed is: 1. A hydrocarbon gas reforming supported catalyst comprising: (a) a catalytic material capable of catalyzing the production of a gaseous mixture comprising hydrogen and carbon monoxide from a hydrocarbon gas; and (b) a support material comprising an alkaline earth metal/metal oxide compound having a structure of D-E, wherein D is a M 1 or M 1 M 2 , M 1 and M 2 each individually being an alkaline earth metal selected from the group consisting of Mg, Ca, Ba, and Sr, and E is a metal oxide selected from the group consisting of Al 2 O 4 , SiO 2 , ZrO 2 , TiO 2 , and CeO 2 , wherein the catalytic material is chemically bonded to the support material, and wherein the chemical bond is a M1-O bond, where M1 is a metal from the catalyst and oxygen (O) is from the alkaline earth metal/metal oxide compound from the support material. 2. The hydrocarbon gas reforming supported catalyst of claim 1 , wherein D is M 1 and E is Al 2 O 4 . 3. The hydrocarbon gas reforming supported catalyst of claim 2 , wherein the compound is MgAl 2 O 4 , CaAl 2 O 4 , BaAl 2 O 4 , or SrAl 2 O 4 . 4. The hydrocarbon gas reforming supported catalyst of claim 3 , wherein the compound is MgAl 2 O 4 . 5. The hydrocarbon gas reforming supported catalyst of claim 1 , wherein D is M 1 M 2 and E is Al 2 O 4 . 6. The hydrocarbon gas reforming supported catalyst of claim 5 , wherein M 1 M 2 is MgCa, MgBa, MgSr, BaCa, BaSr, or CaSr. 7. The hydrocarbon gas reforming supported catalyst of claim 1 , wherein the supported catalyst comprises at least 1% or more by weight of the catalytic material. 8. The hydrocarbon gas reforming supported catalyst of claim 7 , wherein the supported catalyst comprises at least 80% or more by weight of the support material. 9. The hydrocarbon gas reforming supported catalyst of claim 8 , wherein the supported catalyst comprises 5% to 50% by weight of the catalytic material and 95% to 50% by weight of the support material. 10. The hydrocarbon gas reforming supported catalyst of claim 1 , wherein the support material is in particulate or powdered form. 11. The hydrocarbon gas reforming supported catalyst of claim 10 , wherein the particle size of the support material ranges from 5 to 300 μm. 12. The hydrocarbon gas reforming supported catalyst of claim 1 , wherein the support material is in non-powdered form or has a fabricated geometry. 13. The hydrocarbon gas reforming supported catalyst of claim 12 , wherein the fabricated geometry is a pellet, foam, honeycomb, or monolith. 14. The hydrocarbon gas reforming supported catalyst of claim 1 , wherein the catalytic material is a metal catalyst or a metal oxide catalyst. 15. The hydrocarbon gas reforming supported catalyst of claim 14 , wherein the metal catalyst or metal oxide catalyst comprises Pt, Pd, Au, Ag, Ir, Ni, Co, Rh, Ru, La, Mg, Ca, Sr, Ba, Li, Na, K, Fe, Sn, Cu, Zn, Zr, Mo, Nb, Bi, or Mn, or any combination thereof. 16. The hydrocarbon gas reforming supported catalyst of claim 15 , wherein the metal catalyst comprises Ni, Pt, Rh, or Ru or any combination thereof. 17. The hydrocarbon gas reforming supported catalyst of claim 15 , wherein the catalyst comprises Ni and Pt and the catalyst has the following formula: 7.5 wt. % Ni/2.5 wt. % Pt/MgAl 2 O 4 . 18. The hydrocarbon gas reforming supported catalyst of claim 15 , wherein the catalyst comprises Ni and Rh and the catalyst has the following formula: 7.5 wt. % Ni/2.5 wt. % Rh/MgAl 2 O 4 . 19. The hydrocarbon gas reforming supported catalyst of claim 1 , wherein the catalytic material comprises La and Ni and the support material comprises MgAl 2 O 4 . 20. The hydrocarbon gas reforming supported catalyst of claim 19 , wherein the catalyst has the following formula: 11.5 wt. % La/4.8 wt. % Ni/MgAl 2 O 4 . 21. The hydrocarbon gas reforming supported catalyst of claim 1 , wherein the catalytic material is dispersed on the surface of the support material. 22. The hydrocarbon gas reforming supported catalyst of claim 1 , wherein the supported catalyst is capable of reducing carbon formation on the surface of said supported catalyst when subjected to temperatures at a range of greater than 700° C. to 1100° C. 23. The hydrocarbon gas reforming supported catalyst of claim 1 , wherein the supported catalyst is capable of reducing sintering of the catalytic material or of the support material when subjected to temperatures at a range of greater than 700° C. to 1100° C. 24. The hydrocarbon gas reforming supported catalyst of claim 1 , wherein the catalytic material comprises a pyrochlore of: A x B y-z C z O 7 wherein, A is a trivalent ion of an element of La, Ce, Nd, Bi, Sc, or Y, where 0≦x≦2, B is a tetravalent ion of an element of Zr, Pt, Pd, Ni, Mo, Rh, Ru, or Ir, where 0≦y-z≦2, C is a bivalent, trivalent or tetravalent ion of Ba, Ca, Cu, Mg, Ru, Rh, Pt, Pd, Ni, Co, or Mo, where 0≦z≦2. 25. The hydrocarbon gas reforming supported catalyst of claim 1 , wherein the catalytic material comprises La 2 Ni 0.11 Zr 1.89 O 7 and the support material comprises MgAl 2 O 4 . 26. The hydrocarbon gas reforming supported catalyst of claim 1 , wherein the hydrocarbon gas is methane. 27. The hydrocarbon gas reforming supported catalyst of claim 1 , wherein the catalyst is not Ni/MgAl 2 O 4 . 28. A method of producing the hydrocarbon gas reforming supported catalyst of claim 1 comprising: obtaining a compositions comprising (a) a continuous phase comprising a solvent and a catalytic material capable of catalyzing the production of a gaseous mixture comprising hydrogen and carbon monoxide from a hydrocarbon gas, wherein the catalytic material is solubilized in the solvent; and (b) a dispersed phase comprising an alkaline earth metal/metal oxide compound in powdered or particulate form, said compound having a structure of D-E, wherein D is a M 1 or M 1 M 2 , M 1 and M 2 each individually being an alkaline earth metal selected from the group consisting of Mg, Ca, Ba, and Sr, and E is a metal oxide selected from the group consisting of Al 2 O 4 , SiO 2 , ZrO 2 , TiO 2 , and CeO 2 ; and evaporating the solvent from said composition, wherein the hydrocarbon gas reforming supported catalyst is produced, and wherein the catalytic material is chemically bonded to the support material, and wherein the chemical bond is a M1-O bond, where M1 is a metal from the catalyst and oxygen (O) is from the alkaline earth metal/metal oxide compound from the support material. 29. A method of catalytically reforming a reactant gas mixture comprising: (a) providing a reactant gas mixture comprising a hydrocarbon and an oxidant; (b) providing the hydrocarbon gas reforming supported catalyst of claim 1 ; and (c) contacting the reactant gas mixture with the hydrocarbon gas reforming supported catalyst under conditions sufficient to produce a gaseous mixture comprising carbon monoxide and hydrogen. 30. The method of claim 29 , wherein the hydrocarbon comprises methane and the oxidant comprises carbon dioxide or a mixture of carbon dioxide and oxygen. 31. The method of claim 30 , wherein the ratio of carbon monoxide to hydrogen in the produced gaseous mixture is approximately 1. 32. The method of claim 31 , wherein the hydrocarbon comprises methane and the oxidant comprises water.
with rare earths or actinides · CPC title
X-ray diffraction · CPC title
Scanning electron microscopy; Transmission electron microscopy · CPC title
Pyrochlore-type A2B2O7 · CPC title
the reforming step being a carbon dioxide reforming step · CPC title
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