IP Library Granted Patent US 8,834,835
Granted Patent B2
US 8,834,835 · App. 13/751,394 · Granted Sep 16, 2014

Ultra high temperature shift catalyst with low methanation

Inventors: Jon P. Wagner (Louisville, KY); Michael W. Balakos (Buckner, KY); Chandra Ratnasamy (Louisville, KY)
Assignees: Clariant Corporation; L'Air Liquide, Société Anonyme pour l'Etude et l'Exploitation des Procédés Georges Claude
C01B3/16B01J23/10B01J23/36B01J35/1014B01J35/1019Y10S502/524B01J21/06B01J21/066
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Quick Facts
Patent No.
US 8,834,835
App. No.
13/751,394
Granted
Sep 16, 2014
Kind
B2
Abstract

A catalytic water gas shift process at temperatures above about 450° C. up to about 900° C. or so wherein the catalyst includes rhenium deposited on a support, preferably without a precious metal, wherein the support is prepared from a high surface area material, such as a mixed metal oxide, particularly a mixture of zirconia and ceria, to which may be added one or more of a high surface area transitional alumina, an alkali or alkaline earth metal dopant and/or an additional dopant selected from Ga, Nd, Pr, W, Ge, Fe, oxides thereof and mixtures thereof.

Claims (29)

1. A high temperature water gas shift process comprising

preparing a feed stream comprising carbon monoxide and steam, and

passing that feed stream over a water gas shift catalyst at a temperature from about 450° C. to about 900° C.,

wherein the catalyst comprises rhenium deposited on a support and wherein the support comprises a high surface area material with a surface area from about 30 m 2 /g to about 200 m 2 /g.

2. The water gas shift process of claim 1 , wherein the high surface area material of the support comprises two or more metal oxides selected from the group consisting of oxides of cerium, zirconium, lanthanum, yttrium, praseodymium, neodymium, samarium, tungsten, barium, strontium and molybdenum and mixtures thereof.

3. The water gas shift process of claim 1 , wherein the high surface area material of the support comprises a mixed metal oxide comprising two or more metal oxides selected from the group consisting of zirconia, ceria, praseodymia and neodymia.

4. The water gas shift process of claim 1 , wherein the high surface area material of the support comprises a transitional phase, high surface area promoted alumina, wherein the alumina is promoted with an oxide selected from oxides of cerium, zirconium, lanthanum, yttrium, praseodymium, neodymium, samarium, tungsten, barium, strontium and molybdenum and mixtures thereof.

5. The water gas shift process of claim 1 , wherein the catalyst does not include platinum, palladium, rhodium or ruthenium.

6. The water gas shift process of claim 1 , wherein rhenium comprises from about 0.05 to about 10% of the catalyst, by weight.

7. The water gas shift process of claim 1 , wherein the support for the catalyst further comprises praseodymium oxide or neodymium oxide or both.

8. The water gas shift process of claim 1 wherein the catalyst further comprises an alkali or alkaline earth metal dopant.

9. The water gas shift process of claim 8 , wherein the dopant of the catalyst is selected from the group of consisting of oxides of sodium, potassium, cesium, and rubidium and mixtures thereof.

10. The water gas shift process of claim 8 , wherein the dopant of the catalyst comprises from about 0.1 to about 10% of the catalyst, by weight.

11. The water gas shift process of claim 1 , wherein a dopant is added to the catalyst, and wherein the dopant is selected from the group consisting of Ga, Nd, Pr, W, Ge and Fe, their oxides and mixtures thereof.

12. The water gas shift process of claim 1 wherein the feed stream is passed over the water gas shift catalyst at a temperature from about 550° C. to 900° C.

13. A high temperature water gas shift process comprising

preparing a feed stream comprising carbon monoxide and steam, and

passing that feed stream over a water gas shift catalyst at a temperature from about 450° C. to about 900° C.,

wherein the water gas shift catalyst comprises rhenium deposited on a support, wherein the support comprises a mixture of metal oxides comprising zirconia and ceria, and wherein the catalyst does not include any precious metal from the group consisting of platinum, palladium, rhodium, ruthenium, iridium, osmium, silver, gold and mixtures thereof.

14. The water gas shift process of claim 13 , wherein the metal oxides of the support further comprise praseodymium oxide or neodymium oxide.

15. The water gas shift process of claim 13 wherein the feed stream is passed over the water gas shift catalyst at a temperature from about 550° C. to 900° C.

16. A high temperature water gas shift process comprising

preparing a feed stream comprising carbon monoxide and steam, and

passing that feed stream over a water gas shift catalyst at a temperature from about 450° C. to about 900° C.,

wherein the catalyst comprises rhenium on a support, wherein the support comprises two or more metal oxides selected from the group consisting of ceria, zirconia, praseodymia and neodymia, and an alkali or alkaline earth metal dopant, and wherein the catalyst does not include any precious metal selected from the group consisting of platinum, palladium, rhodium, ruthenium, iridium, osmium, silver, gold and mixtures thereof.

17. The water gas shift process of claim 16 , wherein rhenium comprises from about 0.05 to about 10% of the catalyst, by weight.

18. The water gas shift process of claim 16 , wherein the high surface area material of the support comprises ceria and zirconia.

19. The water gas shift process of claim 16 , wherein a dopant is added to the catalyst, and wherein the dopant is selected from the group consisting of Ga, Nd, Pr, W, Ge and Fe, their oxides and mixtures thereof.

20. The water gas shift process of claim 16 wherein the feed stream is passed over the water gas shift catalyst at a temperature from about 550° C. to 900° C.

Assignments (1)
MERGER Recorded Apr 11, 2013
From: SUD-CHEMIE INC.
To: CLARIANT CORPORATION
Reel/Frame 030195/0595 →
Continuity (3)
Division 13358832 · Jan 26, 2012
Division 12048673 · Mar 14, 2008
Related Publication 20130134359A1 · May 30, 2013