METHODS FOR ENHANCING THE EFFICIENCY OF RHENIUM-PROMOTED EPOXIDATION CATALYSTS AND EPOXIDATION METHODS UTILIZING THESE

• US 20100267973A1
• Filed: 04/05/2010
• Published: 10/21/2010
• Est. Priority Date: 04/21/2009
• Status: Active Grant

• Current Assignee: Dow Technology Investments LLC (Dow, Inc.)
• Original Assignee: Dow Technology Investments LLC (Dow, Inc.)
• Inventors: Zhang, Liping, Liu, Albert C.
• Granted Patent: US 8,084,632 B2
• Time in Patent Office: Days
• US Class Current: 549/523
• CPC Class Codes: C07D 301/10 with catalysts containing silver or gold

Abstract

A method for enhancing the efficiency of a rhenium-promoted epoxidation catalyst is provided. Advantageously, the method may be carried out in situ, i.e., within the epoxidation process, and in fact, may be carried out during production of the desired epoxide. As such, a method for the epoxidation of alkylenes incorporating the efficiency-enhancing method is also provided, as is a method for using the alkylene oxides so produced for the production of 1,2-diols, 1,2-carbonates, 1,2-diol ethers, or alkanolamines.

Claims

1. A method for enhancing the efficiency of a rhenium-promoted epoxidation catalyst in situ comprising contacting the catalyst with a feed comprising a gas phase epoxidation reaction promoter at an elevated temperature of at least about 240°

C. for at least about 2 hours and then reducing the temperature to a reduced temperature of less than or equal to about 230°

C.

2. The method of claim 1, wherein the epoxidation catalyst further comprises one or more additional promoters comprising lithium, sodium, potassium, rubidium, cesium, beryllium, magnesium, calcium, strontium, barium, nitrogen, sulfur, manganese, tantalum, molybdenum and tungsten.

3. The method of claim 2, wherein the one or more additional promoters comprise(s) cesium.

4. The method of claim 1, wherein the gas phase epoxidation reaction promoter comprises an organic halide.

5. The method of claim 4, wherein the organic halide comprises chloride.

6. The method of claim 5, wherein the organic halide comprises methyl chloride, ethyl chloride, ethylene dichloride, vinyl chloride, or any combination of two or more of these.

7. The method of claim 1, wherein the feed further comprises oxygen, ethylene, carbon dioxide, water, or any combination of these.

8. The method of claim 1, wherein the efficiency of the epoxidation catalyst is increased by at least about 0.5%.

9. The method of claim 8, wherein the efficiency of the epoxidation catalyst is increased by at least about 1.0%.

10. The method of claim 1, wherein the elevated temperature is less than, or equal to, about 250°

C.

11. The method of claim 1, wherein the gas phase promoter concentration in the feed remains the same at the elevated and reduced temperatures.

12. The method of claim 11, wherein the gas phase promoter concentration in the feed is caused to differ at the elevated and reduced temperatures.

13. A method for the epoxidation of one or more alkylenes comprising contacting a rhenium-promoted epoxidation catalyst with a feed comprising a gas phase epoxidation reaction promoter, oxygen and one or more alkylenes at an elevated temperature of at least about 240°

C. for at least about 2 hours, and subsequently reducing the temperature to a reduced temperature of less than or equal to about 230°

C.

14. The method of claim 13, wherein the feed further comprises carbon dioxide.

15. The method of claim 13, wherein the alkylene comprises ethylene.

16. The method of claim 13, wherein the concentration of the gas phase promoter, oxygen and one or more alkylenes remains the same at the elevated and reduced temperatures.

17. The method of claim 13, wherein the concentration of at least one of the gas phase promoter, oxygen and/or one or more alkylenes is caused to differ at the elevated and reduced temperatures.

18. The method of claim 17, wherein the concentration of at least two of the gas phase promoter, oxygen and/or one or more alkylenes is caused to differ at the elevated and reduced temperatures.

19. A method for making a 1,2-diol, a 1,2-diol ether, a 1,2-carbonate, or an alkanolamine comprising converting an alkylene oxide into the 1,2-diol, a 1,2-diol ether, a 1,2-carbonate, or alkanolamine, wherein the alkylene oxide has been prepared by a method for the epoxidation of alkylenes comprising contacting a rhenium-promoted epoxidation catalyst with a feed comprising a gas phase epoxidation reaction promoter, oxygen and one or more alkylenes at an elevated temperature of at least about 240°

C. for at least about 2 hours, and subsequently reducing the temperature to a reduced temperature of less than or equal to about 230°

C.