IP Library Granted Patent US 10,512,902
Granted Patent B2
US 10,512,902 · App. 16/063,647 · Granted Dec 24, 2019

Carbonylation process using a pretreated zeolite catalyst

Inventors: Nicholas John Hazel (Beverley, GB); David John Law (Hull, GB)
Assignee: BP Chemicals Limited
B01J29/18B01J29/50B01J29/65B01J29/70B01J38/06C07C67/37C07C69/12B01J29/90B01J38/04B01J2229/24B01J2229/34B01J2229/36B01J2229/42Y02P20/584
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Quick Facts
Patent No.
US 10,512,902
App. No.
16/063,647
Granted
Dec 24, 2019
Kind
B2
Abstract

A carbonylation process in the presence of a pretreated zeolite catalyst which comprises the sequential steps (i) pretreating the catalyst and (ii) carbonylating dimethyl ether with a carbon monoxide-containing gas to produce methyl acetate in which the catalyst pretreatment step (i) comprises a step (a) contacting the catalyst with a first treatment mixture comprising water vapour; and a step (b) contacting the treated catalyst of step (a) with a second treatment mixture comprising an inert gas and at least one of dimethyl ether and methanol.

Claims (24)

1. A process for the carbonylation of dimethyl ether with a carbon monoxide-containing gas in the presence of a zeolite carbonylation catalyst which process comprises the sequential steps of:

(i) pretreating the catalyst; and

(ii) carbonylating the dimethyl ether with the carbon monoxide-containing gas to produce a reaction product comprising methyl acetate;

wherein the pretreatment of the catalyst in step (i) comprises the steps:

(a) contacting the catalyst with a first treatment mixture comprising water vapour;

(b) contacting the catalyst treated in step (a) with a second treatment mixture comprising an inert gas and at least one of dimethyl ether and methanol; and

(c) ceasing the inert gas component of the second treatment mixture.

2. A process according to claim 1 wherein the first treatment mixture is a mixture of water vapour and one or more inert gases.

3. A process according to claim 1 wherein the second treatment mixture further comprises water vapour.

4. A process according to claim 2 wherein the second treatment mixture comprises water vapour at a partial pressure in the range 0.8 to 8 bar (80 to 800 kPa).

5. A process according to claim 3 wherein the process further comprises during step (b), a step (b i ) ceasing the water vapour and continuing treatment with the inert gas and the at least one of dimethyl ether and methanol.

6. A process according to claim 5 wherein step (b) is carried out for a period of 1 minute to 1 hour prior to step (b i ).

7. A process according to claim 5 wherein prior to step (c) the at least one of dimethyl ether and methanol is discontinued.

8. A process according to claim 1 wherein the second treatment mixture comprises dimethyl ether in an amount of 1 to 20 mol %.

9. A process according to claim 1 wherein each of steps (a) and (b) is carried out at a temperature in the range 250° C. to 350° C.

10. A process according to claim 1 wherein the zeolite has at least one channel which is defined by an 8-membered ring.

11. A process according to claim 10 wherein the zeolite has a framework type selected from MOR, FER, OFF and GME.

12. A process according to claim 10 wherein the zeolite is mordenite.

13. A process according to claim 1 wherein the zeolite is composited with a binder material.

14. A process according to claim 12 wherein the binder material is an inorganic oxide selected from aluminas, silica-aluminas and silicas.

15. A process according to claim 1 wherein the carbon monoxide-containing gas is a mixture of hydrogen and carbon monoxide.

16. A process according to claim 15 wherein hydrogen and carbon monoxide are present in the mixture in a hydrogen to carbon monoxide molar ratio in the range 1 to 12:1.

17. A process according to claim 1 wherein the carbonylation step (ii) is carried out at a temperature in the range 250° C. to 350° C.

18. A process according to claim 1 wherein methyl acetate is recovered from the reaction product of step (ii) 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 Jun 18, 2018
From: HAZEL, NICHOLAS JOHN; LAW, DAVID JOHN
To: BP CHEMICALS LIMITED
Reel/Frame 046122/0897 →