IP Library Granted Patent US 9,505,703
Granted Patent B2
US 9,505,703 · App. 14/773,034 · Granted Nov 29, 2016

Carbonylation process

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,505,703
App. No.
14/773,034
Granted
Nov 29, 2016
Kind
B2
Abstract

Process for the production of methyl acetate by carbonylating dimethyl ether with carbon monoxide in the presence of hydrogen and a zeolite catalyst. The process is carried out with a molar ratio of hydrogen to carbon monoxide of at least 1 and the catalyst has been calcined at a temperature of from about 375° C. to about 475° C.

Claims (29)

1. A process for the production of methyl acetate which comprises carbonylating dimethyl ether with carbon monoxide in the presence of hydrogen and a zeolite catalyst wherein the process is carried out with a molar ratio of hydrogen to carbon monoxide of at least 1 and the catalyst has been calcined at a temperature of from about 375° C. to about 475° C.

2. A process for improving the performance of a zeolite catalyst in the production of methyl acetate by the carbonylation of dimethyl ether with carbon monoxide in the presence of hydrogen wherein the process is carried out with a molar ratio of hydrogen to carbon monoxide of at least 1 and the catalyst has been calcined at a temperature of from about 375° C. to about 475° C.

3. A process according to claim 1 wherein the process is initially conducted with a carbon monoxide to hydrogen molar ratio of at least 1 and thereafter carried out with an hydrogen to carbon monoxide molar ratio of at least 1.

4. A process according to claim 3 wherein the process is initially conducted with a carbon monoxide to hydrogen molar ratio in the range 1 to 4:1 and thereafter carried out with an hydrogen to carbon monoxide molar ratio in the range 1 to 2:1.

5. A process according to claim 1 wherein the catalyst is calcined at a temperature of from about 400° C. to about 475° C.

6. A process according to claim 5 wherein the catalyst is calcined at a temperature of from about 400° C. to about 450° C.

7. A process according to claim 1 wherein the catalyst is calcined in an inert atmosphere or in an oxidising atmosphere.

8. A process according to claim 7 wherein the oxidising atmosphere is air.

9. A process according to claim 1 wherein the catalyst is calcined for a duration of from about 10 minutes to about 10 hours.

10. A process according to claim 9 wherein the catalyst is calcined for a duration of from about 1 hour to about 3 hours.

11. A process according to claim 1 wherein the molar ratio of hydrogen to carbon monoxide is in the range 1 to 10:1.

12. A process according to claim 11 wherein the molar ratio of hydrogen to carbon monoxide is 1 to 2:1.

13. A process according to claim 1 wherein the zeolite contains at least one channel or pocket which is defined by an 8-member ring and the 8-member ring channel or pocket is interconnected with at least one channel defined by a ring with 10 or 12 members.

14. A process according to claim 13 wherein the zeolite is selected from zeolites of framework type MOR, FER, OFF, CHA, GME and MFS.

15. A process according to claim 13 wherein the zeolite is selected from mordenite, ferrierite and offretite.

16. A process according to claim 15 wherein the zeolite is a mordenite in a hydrogen-exchanged or an ammonium-exchanged form.

17. A process according to claim 1 wherein the zeolite is combined with a binder.

18. A process according to claim 17 wherein the binder is a refractory inorganic oxide binder.

19. A process according to claim 18 wherein the refractory inorganic oxide binder is selected from aluminas, silica-aluminas or silicas.

20. A process according to claim 17 wherein the binder is present in an amount of 10% to 30% by weight.

21. A process according to claim 17 wherein the zeolite combined with the binder is in the form of an extrudate.

22. A process according to claim 1 wherein the process is carried out at a concentration of water of less than 1 mol % based on the total gaseous feed to the process.

23. A process according to claim 1 wherein synthesis gas is used as the source of carbon monoxide and hydrogen.

24. A process according to claim 1 wherein the process is carried out at a temperature in the range 200° C. to 350° C.

25. A process according to claim 24 wherein the process is carried out at a temperature in the range 280° C. to 320° C.

26. A process according to claim 1 wherein the process is carried out at a total pressure of from 10 to 100 barg.

27. A process according to claim 1 wherein methyl acetate is introduced into the process in an amount of from 0.05 mol % to 5 mol % based on the total feed to the process.

28. A process according to claim 1 wherein the process is carried out as a vapour phase process.

29. A process according to claim 1 wherein methyl acetate is recovered from the process and some or all of the recovered methyl acetate is converted to acetic acid.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 26, 2021
From: BP CHEMICALS LIMITED
To: INEOS ACETYLS UK LIMITED
Reel/Frame 055746/0075 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 2, 2015
From: DITZEL, EVERT JAN; GAGEA, BOGDAN COSTIN; HAINING (DECEASED), GORDON JOHN; HAZEL, NICHOLAS JOHN; SUNLEY, JOHN GLENN
To: BP CHEMICALS LIMITED
Reel/Frame 036939/0866 →