IP Library Granted Patent US 9,770,706
Granted Patent B2
US 9,770,706 · App. 14/891,212 · Granted Sep 26, 2017

Catalyst composition for the production of syngas from methane, process therefore and process for CO

Inventors: Chandra Mondal Kartick (Vadodara, IN); Mayank Harishbhai Vyas (Vadodara, IN); Sankar Sasmal (West Bengal, IN)
Assignee: SAUDI BASIC INDUSTRIES CORPORATION
B01J23/78B01J35/10B01J35/1038B01J35/1061B01J37/0036B01J37/0201B01J37/0236B01J37/08C01B3/40C01B2203/0238C01B2203/1052C01B2203/1058C01B2203/1082C01B2203/1094C01B2203/1241Y02P20/52
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Quick Facts
Patent No.
US 9,770,706
App. No.
14/891,212
Granted
Sep 26, 2017
Kind
B2
Abstract

A catalyst for performing carbon dioxide reforming of methane to produce syngas, that includes cobalt, nickel and magnesium oxides disposed a support.

Claims (38)

1. A CO 2 reforming supported catalyst, comprising oxides of cobalt, nickel, and magnesium disposed on a support comprising alumina, niobia, silica, tantalum oxide, tin oxide, titania, or a combination comprising at least one of the foregoing oxides; and a promoter, wherein the promoter is lanthanum or cerium, wherein the amount of the promoter is from more than 0.001 to less than 0.5 mol % relative to the supported catalyst.

2. The supported catalyst claim 1 , wherein the support has an average pore diameter of 5 to 13 nm.

3. The supported catalyst of claim 1 , wherein the supported catalyst has an average pore volume from 0.06 cm 3 /g to 0.5 cm 3 /g.

4. The supported catalyst of claim 1 , wherein the support is an alumina-silica support.

5. The supported catalyst of claim 1 , wherein no zirconia is present.

6. The supported catalyst of claim 1 , wherein the catalyst exhibits hydrogen selectivity equal to or greater than 97% in CO 2 reforming.

7. The supported catalyst of claim 1 , wherein the catalyst provides equal to or greater than 96% methane conversion in CO 2 reforming.

8. The supported catalyst of claim 1 , wherein the catalyst provides in equal to or greater than 91% carbon dioxide conversion in CO 2 reforming.

9. A process for the preparation of the CO 2 reforming supported catalyst of claim 1 , the process comprising:

combining a templating copolymer and a support precursor in a solvent to form a support solution;

dissolving salts comprising nickel, cobalt, and magnesium in a solvent to form a metal solution;

combining the support solution and the metal solution;

adding a promoter, wherein the promoter is lanthanum or cerium;

adding an acid to form a catalyst solution;

heating the catalyst solution at a temperature effective to form a solid catalyst mass;

grinding the solid catalyst mass into a powdered catalyst; and

calcining the powdered catalyst in the presence of oxygen to provide the CO 2 reforming supported catalyst.

10. The process of claim 9 , wherein the process further comprises subjecting the calcined, supported catalyst to a gas stream that comprises hydrogen to reduce the CO 2 reforming supported catalyst.

11. The process of claim 9 , wherein the support solution comprises an aluminum compound and a silica compound.

12. The process of claim 9 , wherein no zirconium compound is present.

13. A process for CO 2 reforming of lower alkanes to a synthesis gas comprising H 2 and CO, the process comprising

subjecting a feedstream of gaseous lower alkanes to CO 2 in the presence of the catalyst of claim 1 at a temperature and pressure effective to reform the CO 2 .

14. The process of claim 13 , wherein the feedstream of gaseous lower alkanes comprises methane.

15. The process of claim 13 , wherein the feedstream comprises a carbon dioxide:methane mole ratio of 1.1.

16. The process of claim 13 , wherein the synthesis gas comprises a H 2 :CO ratio from 0.95 to 1.0.

17. A CO 2 reforming supported catalyst, comprising oxides of cobalt, nickel, and magnesium disposed on a support, wherein the amount of magnesium is between 0.05 and 2.5 mol % relative to the supported catalyst and a promoter, wherein the promoter is lanthanum or cerium, wherein the amount of the promoter is from more than 0.001 to less than 0.5 mol % relative to the supported catalyst.

18. The supported catalyst of claim 17 , wherein the support comprises alumina, niobia, silica, tantalum oxide, tin oxide, titania, zirconia, or a combination comprising at least one of the foregoing oxides.

19. A process for the preparation of the CO 2 reforming supported catalyst of claim 18 , the process comprising:

providing a support comprising alumina, niobia, silica, tantalum oxide, tin oxide, titania, zirconia, or a combination comprising at least one of the foregoing oxides; and

impregnating the support with a solution comprising salts of nickel, cobalt, and magnesium;

adding a promoter, wherein the promoter is lanthanum or cerium;

drying the impregnated support; and

calcining the impregnated, dried support at a temperature above 500° C.

20. The process of claim 19 , wherein the process further comprises subjecting the calcined, supported catalyst to a gas stream that comprises hydrogen to reduce the CO 2 reforming supported catalyst.

21. The process of claim 19 , wherein the support comprises alumina-silica.

22. The process of claim 19 , wherein no zirconia is present in the support.

23. A CO 2 reforming supported catalyst, comprising a mixed metal oxide catalyst component of the formula NiCoMgO x disposed on a support; and a promoter, wherein the promoter is lanthanum or cerium, wherein the amount of the promoter is from more than 0.001 to less than 0.5 mol % relative to the supported catalyst.

24. The supported catalyst of claim 23 , wherein the support comprises alumina, niobia, silica, tantalum oxide, tin oxide, titania, zirconia, or a combination comprising at least one of the foregoing oxides.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 17, 2015
From: KARTICK, CHANDRA MONDAL; VYAS, MAYANK HARISHBHAI; SASMAL, SANKAR
To: SAUDI BASIC INDUSTRIES CORPORATION
Reel/Frame 037057/0239 →
Priority Claims (1)
EP 13170906 · Jun 6, 2013 · regional
Continuity (2)
Provisional Application 61896902 · Oct 29, 2013
Related Publication 20160121305A1 · May 5, 2016