IP Library Granted Patent US 7,799,229
Granted Patent B2
US 7,799,229 · App. 11/596,590 · Granted Sep 21, 2010

Process for the removal of catalytic metals and promoter metals from carbonylation process streams

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Quick Facts
Patent No.
US 7,799,229
App. No.
11/596,590
Granted
Sep 21, 2010
Kind
B2
Abstract

Process for the selective removal of Iridium carbonylation catalyst metal and/or at least one promoter selected from ruthenium, osmium and rhenium from a liquid composition comprising a carbonylation product, iridium carbonylation catalyst metal and/or the promoter metal, corrosion metals and optionally alkali or alkaline earth metals. The process is carried out by contacting the liquid composition with a chelating resin to remove at least a portion of the iridium carbonylation catalyst metal and/or at least one promoter metal contained in the liquid composition. The chelating resin contains at least one thiourea functional group. The process is suitable for treating process streams obtained in the production of carboxylic acids and/or carboxylic anhydrides.

Claims (27)

1. A process for the selective removal of Iridium carbonylation catalyst metal and/or at least one promoter selected from the group consisting of ruthenium, osmium and rhenium from a liquid composition comprising a carbonylation product, iridium carbonylation catalyst metal and/or said promoter metal, corrosion metals and optionally alkali or alkaline earth metals which process comprises contacting said liquid composition with a chelating resin to remove at least a portion of the iridium carbonylation catalyst metal and/or at least one promoter metal contained in the liquid composition and wherein the chelating resin comprises at least one thiourea functional group.

2. A process according to claim 1 wherein the liquid composition comprises alkali or alkaline earth metals.

3. A process according to claim 2 wherein the alkali metal is selected from the group consisting of lithium, sodium and potassium.

4. A process according to claim 1 wherein the chelating resin is of formula:

wherein P represents a chemical backbone.

5. A process according to claim 4 wherein the chemical backbone, P, is a polymer.

6. A process according to claim 5 wherein the polymer is selected from the group consisting of polystyrene, polyacrylate, polymethacrylate, polyethylene and polypropylene.

7. A process according to claim 5 or claim 6 wherein the polymer is a crosslinked polymer.

8. A process according to claim 7 wherein the crosslinked polymer is a crosslinked polystyrene.

9. A process according to claim 8 wherein the crosslinked polystyrene is a divinylbenzene polystyrene.

10. A process according to claim 4 wherein the chemical backbone, P, is selected from the group consisting of silica, alumina, titania, ceria, zirconia, clays and zeolites.

11. A process according to claim 4 wherein the chemical backbone, P, has inorganic and organic moieties.

12. A process according to claim 1 wherein the chelating resin is a macroporous resin or a gel resin.

13. A process according to claim 1 wherein the liquid reaction composition further comprises rhodium carbonylation catalyst metal.

14. A process according to claim 1 wherein the process is operated as a batch, semi-continuous or continuous process.

15. A process according to claim 1 wherein the liquid composition is contacted with the chelating resin at a temperature in the range 0 to 100° C.

16. A process according to claim 1 wherein the liquid hourly space velocity of the liquid composition is in the range 1 to 20 h −1 .

17. A process according to claim 1 wherein the liquid composition is treated in-situ or offline.

18. A process according to claim 1 wherein the liquid composition is a process stream obtained from a carbonylation process to produce a carbonylation product which is a carboxylic acid.

19. A process according to claim 18 wherein the carboxylic acid is acetic acid.

20. A process according to claim 1 wherein the liquid composition further comprises one or more components selected from the group consisting of unconverted carbonylatable reactant, a solvent, water and iodide ions.

21. A process according to claim 1 wherein the liquid composition is a process stream obtained from the carbonylation of an alcohol and/or reactive derivative thereof in the presence of an iridium carbonylation catalyst, an alkyl halide co-catalyst, a catalyst promoter selected from ruthenium, osmium and rhenium and optionally a finite concentration of water.

22. A process according to claim 21 wherein the alcohol is methanol, the alkyl halide is methyl iodide, and the carbonylation is conducted with a finite concentration of water.

23. A process according to claim 1 wherein the liquid composition is to be treated is obtained from a distillation column stream.

24. A process according to claim 23 wherein the distillation column stream is selected from the group consisting of a stream from the base of a heavy ends column, a stream from the base of a combined light ends and drying column and a stream from a drying column.

25. A process according to claim 1 wherein the liquid composition is obtained from a gas phase carbonylation process.

26. A process according to claim 1 wherein the corrosion metal is selected from the group consisting of iron, nickel, chromium, manganese, zinc, molybdenum and mixtures thereof.

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 15, 2006
From: POOLE, ANDREW DAVID; SMITH, STEPHEN JAMES
To: BP CHEMICALS LIMITED
Reel/Frame 018726/0363 →