Catalytic process for the conversion of a synthesis gas to hydrocarbons

Patent metadata

Field	Value
Publication number	US-9493381-B2
Application number	US-201214123235-A
Country	US
Kind code	B2
Filing date	May 31, 2012
Priority date	Jun 1, 2011
Publication date	Nov 15, 2016
Grant date	Nov 15, 2016

Abstract

Catalytic process for the partial conversion of a gaseous mixture containing carbon monoxide and hydrogen into a mixture of hydrocarbons, including bringing the said gaseous mixture into contact with a solid catalyst, the solid catalyst having a porous support with a composite material including SiC and a titanium carbide and/or a titanium oxide, and an active phase. The support is prepared in the form of grains, beads, or extrudates, or in the form of cylinders or sheets of cellular foam.

First claim

The invention claimed is:

1. A process of at least partial catalytic conversion of a gaseous mixture containing CO and H 2 to a mixture of hydrocarbons, comprising a step of placing said gaseous mixture in contact with a solid catalyst, said solid catalyst comprising:
a porous support comprising at least one of a composite material comprising SiC and titanium carbide, and a composite material comprising SiC and titanium oxide, and
an active phase,
wherein said porous support has a molar content of titanium with respect to the molar sum of Si+Ti of between 0.5% and 15%.

2. The process according to claim 1 , wherein said composite material has been prepared by a method including the preparation of a mixture comprising at least one silicon source, at least one carbon source and at least one titanium source, this preparation being followed by at least one heat treatment that is intended to transform said silicon source at least partially into silicon carbide and at least part of said titanium source into titanium carbide, said heat treatment being at least partially performed at a temperature of between 1200° C. and 1450° C.

3. The process according to claim 2 , wherein said method for preparing said composite material also includes a step of additional oxidation at a temperature of at least 350° C., in order to partially or totally transform the titanium carbide into titanium dioxide.

4. The process according to claim 1 , wherein the content of active phase with respect to the total mass of said porous support with its active phase is between 1 and 50% by mass.

5. The process according to claim 1 , wherein said active phase includes primarily cobalt or primarily iron.

6. The process according to claim 5 ,
wherein iron is present in the active phase that includes primarily cobalt; and
wherein cobalt is present in the active phase that includes primarily iron.

7. The process according to claim 5 , wherein said active phase further comprises at least one transition metal selected from the group consisting of Groups 7, 8, 9, and 10.

8. The process according to claim 1 , wherein said active phase includes a promoter with a content not exceeding 2% by mass.

9. The process according to claim 8 , wherein said promoter is selected from the group consisting of rare earth elements and oxides thereof, alkaline earth elements and oxides thereof, and transition metals and oxides thereof.

10. The process according to claim 9 , wherein the transition metals are selected from the group consisting of ruthenium, platinum, rhenium, rhodium, iridium, and palladium.

11. The process according to claim 1 , wherein said porous support has a specific BET surface area greater than 5 m 2 /g.

12. The process according to claim 1 , wherein said porous support has a microporous surface area greater than 10 m 2 /g.

13. The process according to claim 12 , wherein said porous support has a porous volume in the range of 30 nm and 300 nm measured by mercury intrusion greater than 0.12 cm 3 /g.

14. The process according to claim 1 , wherein said support is in the form of pellets, beads, extrudates, or in the form of a cellular foam.

15. The process according to claim 3 , wherein said temperature is at least 400° C.

16. The process according to claim 4 , wherein the content of active phase with respect to the total mass of said porous support with its active phase is between 5% and 35%.

17. The process according to claim 4 , wherein the content of active phase with respect to the total mass of said porous support with its active phase is 5% and 30%.

18. The process according to claim 11 , wherein the specific BET surface area is greater than 30 m 2 /g.

19. The process according to claim 11 , wherein the specific BET surface area is greater than 40 m 2 /g.

20. The process according to claim 11 , wherein the specific BET surface area is greater than 60 m 2 /g.

21. The process according to claim 1 , wherein said molar content of titanium is between 0.5% and 10%.

22. The process according to claim 12 , wherein said microporous surface area is greater 20 m 2 /g.

23. The process according to claim 13 , wherein the porous volume is in the range of greater than 0.15 cm 3 /g.

24. The process according to claim 13 , wherein the porous volume is in the range of greater than 0.20 cm 3 /g.

Assignees

• Luck Francis
• Pham Charlotte
• Nguyen Patrick
• Pham-Huu Cuong
• De Tymowski Benoit
• Sicat Llc
• Total Sa
• Centre Nat Rech Scient
• Univ Strasbourg

Inventors

• Luck Francis
• Pham Charlotte
• Nguyen Patrick
• Pham-Huu Cuong
• De Tymowski Benoit

Classifications

• B01J27/224

  Silicon carbide · CPC title

• B01J23/83

  with rare earths or actinides · CPC title

• B01J23/75

  Cobalt · CPC title

• C10G2/332

  of the iron-group · CPC title

• B01J23/8906

  Iron and noble metals · CPC title