IP Library Granted Patent US 11,053,187
Granted Patent B2
US 11,053,187 · App. 16/604,297 · Granted Jul 6, 2021

Process for carbonylating dimethyl ether

Inventor: Thomas Edward Clark (Middlesex, GB)
Assignee: Ineos Acetyls UK Limited
C07C67/37B01J29/18B01J38/52C07C69/14
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Quick Facts
Patent No.
US 11,053,187
App. No.
16/604,297
Granted
Jul 6, 2021
Kind
B2
Abstract

A process for the production of methyl acetate by carbonylating dimethyl ether with carbon monoxide at a temperature of 250 to 350° C. in the presence of a zeolite catalyst and hydrogen such that the molar ratio of hydrogen to carbon monoxide is at least 1, and one or more compounds containing a hydroxyl functional group and in the absence of any added methyl acetate.

Claims (44)

1. A process for the production of methyl acetate by carbonylation of dimethyl ether which process comprises contacting in a reactor dimethyl ether with carbon monoxide in the presence of a zeolite catalyst, hydrogen, and at least one compound containing a hydroxyl functional group at a temperature of from 250 to 350° C. and at a molar ratio of hydrogen to carbon monoxide of at least 1,

wherein the process comprises introducing into the reactor the at least one compound containing a hydroxyl functional group, and the process is carried out in the absence of added methyl acetate;

wherein the at least one compound containing a hydroxyl functional group is one or more hydroxyl compound(s) selected from water, C 1 -C 4 aliphatic alcohols, and C 1 -C 4 aliphatic carboxylic acids; and

wherein the zeolite is a templated zeolite.

2. A process according to claim 1 wherein the hydroxyl compound(s) is introduced into the reactor in a total amount of up to 1 mol % based on a total gaseous feed to the process including the hydroxyl compound(s), dimethyl ether, carbon monoxide, and hydrogen.

3. A process according to claim 2 wherein the total amount of hydroxyl compound(s) is from 0.01 to 0.5 mol % based on the total gaseous feed to the process.

4. A process according to claim 1 , wherein the one or more hydroxyl compound(s) is selected from C 1 -C 4 aliphatic alcohols and C 1 -C 4 aliphatic carboxylic acids.

5. A process according to claim 4 wherein the hydroxyl compound is a C 1 -C 4 aliphatic alcohol.

6. A process according to claim 4 wherein the hydroxyl compound is a C 1 -C 4 aliphatic carboxylic acid.

7. A process according to claim 1 wherein the hydroxyl compound(s) is selected from one or more of acetic acid, methanol and water.

8. A process according to claim 1 , wherein the molar ratio of hydrogen to carbon monoxide is in the range 1.5 to 4:1.

9. A process according to claim 1 , wherein the catalyst is a zeolite having at least one channel which is defined by an 8-membered ring.

10. A process according to claim 9 wherein the zeolite has a framework type selected from the group consisting of MOR, FER, OFF, CHA, GME, MFS, EON and ETR.

11. A process according to claim 10 wherein the zeolite has the framework type MOR and is mordenite.

12. A process according to claim 1 , wherein the process is carried out at a temperature of from 275 to 325° C.

13. A process according to claim 1 , wherein methyl acetate product is hydrolysed to acetic acid.

14. A method of maintaining or reducing the deactivation rate of a catalyst in a process for the production of methyl acetate by carbonylation of dimethyl ether which process comprises contacting in a reactor dimethyl ether with carbon monoxide in the presence of a zeolite catalyst, hydrogen, and at least one compound containing a hydroxyl functional group at a temperature of from 250 to 350° C. and at a molar ratio of hydrogen to carbon monoxide of at least 1,

wherein the process comprises introducing into the reactor the at least one compound containing a hydroxyl functional group and the process is carried out in the absence of added methyl acetate;

wherein the at least one compound containing a hydroxyl functional group is one or more hydroxyl compound(s) selected from water, C 1 -C 4 aliphatic alcohols, and C 1 -C 4 aliphatic carboxylic acids; and

wherein the zeolite is a templated zeolite.

15. A process according to claim 1 , wherein

the molar ratio of hydrogen to carbon monoxide is in the range 1 to 12:1;

the total amount of hydroxyl compound(s) is from 0.01 to 0.5 mol % based on the total gaseous feed to the process; and

the amount of dimethyl ether is from 1.0 to 20 mol % based on the total gaseous feed to the process.

16. A process according to claim 1 , wherein

the molar ratio of hydrogen to carbon monoxide is in the range 1 to 8:1;

the total amount of hydroxyl compound(s) is from 0.01 to 0.5 mol % based on the total gaseous feed to the process; and

the amount of dimethyl ether is from 1.5 to 15 mol % based on the total gaseous feed to the process.

17. A process according to claim 1 , wherein

the molar ratio of hydrogen to carbon monoxide is in the range 1.5 to 4:1;

the total amount of hydroxyl compound(s) is from 0.01 to 0.5 mol % based on the total gaseous feed to the process; and

the amount of dimethyl ether is from 1.5 to 15 mol % based on the total gaseous feed to the process.

18. A process according to claim 1 , wherein

the molar ratio of hydrogen to carbon monoxide is in the range 1.5 to 4:1;

the hydroxyl compound is acetic acid, present in an amount from 0.01 to 0.5 mol % based on the total gaseous feed to the process; and

the zeolite has a framework type selected from the group consisting of MOR, FER, OFF, CHA, GME, MFS, EON and ETR.

19. A process according to claim 1 , wherein

the molar ratio of hydrogen to carbon monoxide is in the range 1.5 to 4:1;

the hydroxyl compound is methanol, present in an amount from 0.01 to 0.5 mol % based on the total gaseous feed to the process; and

the zeolite has a framework type selected from the group consisting of MOR, FER, OFF, CHA, GME, MFS, EON and ETR.

20. A process according to claim 1 , wherein

the molar ratio of hydrogen to carbon monoxide is in the range 1.5 to 4:1;

the hydroxyl compound is water, present in an amount from 0.01 to 0.5 mol % based on the total gaseous feed to the process; and

the zeolite has a framework type selected from the group consisting of MOR, FER, OFF, CHA, GME, MFS, EON and ETR.

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 Oct 10, 2019
From: CLARK, THOMAS EDWARD
To: BP CHEMICALS LIMITED
Reel/Frame 050680/0246 →