IP Library Granted Patent US 7,148,390
Granted Patent B2
US 7,148,390 · App. 10/375,464 · Granted Dec 12, 2006

Integrated process for synthesizing alcohols, ethers, aldehydes, and olefins from alkanes

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Quick Facts
Patent No.
US 7,148,390
App. No.
10/375,464
Granted
Dec 12, 2006
Kind
B2
Abstract

Alcohols, ethers, aldehydes, and olefins are manufactured from alkanes by mixing an alkane and a halogen selected from the group including chlorine, bromine, and iodine in a reactor to form alkyl halide and hydrogen halide. The alkyl halide only or the alkyl halide and the hydrogen halide are directed into contact with metal oxide to form an alcohol and/or an ether, or an olefin and metal halide. The metal halide is oxidized to form original metal oxide and halogen, both of which are recycled.

Claims (36)

1. A method for synthesizing olefins from alkanes comprising:

providing a quantity of an alkane selected from the group consisting of ethane, propane, butane, isobutane, pentanes, cyclohexane and hexanes;

providing a quantity of bromine;

mixing the selected alkane and the bromine and thereby forming an alkyl bromide and hydrogen bromide;

directing the alkyl bromide into engagement with a metal oxide and thereby forming an olefin and a metal bromide;

recovering the thus formed olefin;

converting the metal bromide to form the original metal oxide and bromine;

recycling the metal oxide; and

recycling the bromine.

2. The method according in claim 1 wherein the step of mixing the alkane and the bromine is carried out at a alkane to bromine mol ratio between about 1:10 to about 100:1.

3. The method according to claim 1 wherein the step of mixing the alkane and the bromine is carried out at a alkane to bromine mol ratio between about 1:5 to about 50:1.

4. The method according to claim 1 wherein the step of mixing the alkane and the bromine is carried out at a alkane to bromine mol ratio between about 1:2 to about 10:1.

5. The method according to claim 1 wherein the step of mixing the alkane and the bromine is carried out at a temperature of between about 20° C. and about 600° C.

6. The method according to claim 1 wherein the step of mixing the alkane and the bromine is carried out at a pressure of between 0.1 and 200 atm.

7. The method according to claim 1 wherein the step of mixing the alkane and the bromine to form the alkyl bromide and hydrogen bromide and the step of contacting the alkyl bromide with a metal oxide are carried out continuously.

8. The method according to claim 1 wherein the step of mixing the alkane and the bromine to form the alkyl bromide and hydrogen bromide and the step of contacting the alkyl bromide with a metal oxide are carried out in a batch reaction.

9. The method according to claim 1 wherein the step of converting the metal bromide to form the original metal oxide catalyst and bromine, the step of recycling the metal oxide, and the step of recycling the bromine are carried out continuously.

10. The method according to claim 1 wherein the step of converting the metal bromide to form the original metal oxide catalyst and bromine, the step of recycling the metal oxide, and the step of recycling the bromine are carried out in batch reactions.

11. A method for synthesizing olefins from alkanes comprising:

providing a quantity of an alkane selected from the group consisting of ethane, propane, butane, isobutane, pentanes, cyclohexane and hexanes;

providing a quantity of a halide selected from the group consisting of chlorine, bromine, and iodine;

mixing the selected alkane and the selected halide and thereby forming an alkyl halide and hydrogen halide;

directing the alkyl halide into engagement with a metal oxide and thereby forming an olefin and a metal halide;

recovering the thus formed olefin;

converting the metal halide to form the original metal oxide and the original halide;

recycling the metal oxide; and

recycling the halide.

12. The method according to claim 11 wherein the step of mixing the alkane and the halide is carried out at a alkane to halide mol ratio between about 1:10 to about 100:1.

13. The method according to claim 11 wherein the step of mixing the alkane and the halide is carried out at a alkane to halide mol ratio between about 1:5 to about 50:1.

14. The method according to claim 11 wherein the step of mixing the alkane and the halide is carried out at a alkane to halide mol ratio between about 1:2 to about 10:1.

15. The method according to claim 11 wherein the step of mixing the alkane with the halide is carried out at a temperature of between about 20° C. and about 600° C.

16. The method according to claim 11 wherein the step of mixing the alkane and the halide is carried out at a pressure of between 0.1 and 200 atm.

17. The process according to claim 11 wherein the step of mixing the alkane and the halide to form the alkyl halide and hydrogen halide and the step of contacting the alkyl halide with a metal oxide are carried out continuously.

18. The process according to claim 11 wherein the step of mixing the alkane and the halide to form the alkyl halide and hydrogen halide and the step of contacting the alkyl halide with a metal oxide are carried out in batch reactions.

19. The method according to claim 11 wherein the step of converting the metal halide to form the original metal oxide catalyst and the original halide, the step of recycling the metal oxide, and the step of recycling the halide are carried out continuously.

20. The method according to claim 11 wherein the step of converting the metal halide to form the original metal oxide catalyst and the original halide, the step of recycling the metal oxide, and the step of recycling the halide are carried out in batch reactions.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 9, 2013
From: GRT, INC.
To: REACTION 35, LLC
Reel/Frame 031778/0327 →
RELEASE OF SECURITY INTEREST Recorded Dec 9, 2013
From: HOOK, THOMAS W.
To: REACTION 35, LLC
Reel/Frame 031784/0696 →
SECURITY AGREEMENT Recorded Jul 3, 2012
From: GRT, INC.
To: HOOK, THOMAS W.
Reel/Frame 028498/0541 →