IP Library Granted Patent US 8,247,585
Granted Patent B2
US 8,247,585 · App. 12/836,224 · Granted Aug 21, 2012

Systems and methods for removing catalyst and recovering free carboxylic acids after transesterification reaction

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Quick Facts
Patent No.
US 8,247,585
App. No.
12/836,224
Granted
Aug 21, 2012
Kind
B2
Abstract

Systems and methods for using carbon dioxide to remove an alkali catalyst and to recover free carboxylic acids after a transesterification reaction are disclosed. Generally, the methods include first providing a mixture resulting from the transesterification of an ester, wherein the mixture includes substances selected from the alkali catalyst, an alcohol, and a transesterification reaction product such as biodiesel. Second, the methods generally include adding carbon dioxide to the mixture. In some cases, adding the carbon dioxide to the mixture causes the alkali catalyst to convert into an alkali carbonate and/or an alkali bicarbonate. In other cases, adding the carbon dioxide to the mixture causes the carboxylic acid alkali salt to convert into a free carboxylic acid. In either case, the alkali carbonate, the alkali bicarbonate, and/or the free carboxylic acid can be separated from the mixture in any suitable manner.

Claims (36)

1. A method for removing one or more chemicals after a reaction involving the transesterification of an ester, the method comprising:

providing a mixture resulting from the transesterification of the ester, wherein the mixture comprises an alkali catalyst, an alcohol, and a transesterification reaction product;

adding carbon dioxide to the mixture to convert the alkali catalyst into one or more of an alkali carbonate and an alkali bicarbonate; and

separating the alkali carbonate and/or alkali bicarbonate from the mixture.

2. The method of claim 1 , wherein the mixture resulting from the transesterification further comprises a carboxylic acid alkali salt.

3. The method of claim 2 , wherein the carbon dioxide converts the carboxylic acid alkali salt into a free carboxylic acid and one or more of an alkali carbonate and an alkali bicarbonate.

4. The method of claim 3 , further comprising separating the free carboxylic acid, the alkali carbonate, and/or the alkali bicarbonate from the mixture.

5. The method of claim 1 , wherein the mixture comprises water.

6. The method of claim 1 , wherein the method comprises adding the carbon dioxide to the mixture to convert the alkali catalyst into a solid phase; and separating the solid phase from the mixture.

7. The method of claim 1 , wherein the transesterification reaction product comprises glycerin and biodiesel.

8. The method of claim 1 , wherein the alkali catalyst is selected from sodium hydroxide, potassium hydroxide, magnesium hydroxide, aluminum hydroxide, a sodium alkoxide, a potassium alkoxide, a magnesium alkoxide, and an aluminum alkoxide.

9. The method of claim 8 , wherein the alkali catalyst is selected from an alkali hydroxide and an alkali alkoxide.

10. The method of claim 1 , wherein the alkali catalyst is selected from sodium hydroxide and sodium methoxide.

11. The method of claim 9 , wherein the alkali catalyst comprises an alkali methoxide, and wherein adding the carbon dioxide to the mixture forms an ether and the alkali carbonate.

12. The method of claim 5 , wherein the water, the carbon dioxide, and the alkali carbonate react to form the alkali bicarbonate.

13. The method of claim 1 , wherein the alcohol is selected from methanol and ethanol.

14. The method of claim 1 , wherein the mixture results from the transesterification of a triglyceride.

15. The method of claim 1 , wherein the transesterification product comprises a carboxylic acid ester and an alcohol.

16. The method of claim 1 , wherein the mixture is selected from one or more of a product, an unreacted reactant, and a participant of the transesterification reaction.

17. A method for removing one or more chemicals after a reaction involving the transesterification of an ester, the method comprising:

providing a mixture resulting from the transesterification of the ester, wherein the mixture comprises an alkali catalyst, an alcohol, a transesterification reaction product, a carboxylic acid alkali salt, and water;

adding carbon dioxide to the mixture to convert the alkali catalyst into one or more of an alkali carbonate and an alkali bicarbonate and to convert the carboxylic acid alkali salt into a free carboxylic acid and one or more of an alkali carbonate and an alkali bicarbonate;

separating the alkali carbonate and/or alkali bicarbonate from the mixture; and

separating the free carboxylic acid from the mixture.

18. The method of claim 17 , wherein the method comprises adding the carbon dioxide to the mixture to convert the alkali catalyst into a solid phase; and separating the solid phase from the mixture.

19. The method of claim 17 , wherein the alkali catalyst is selected from sodium hydroxide, potassium hydroxide, magnesium hydroxide, aluminum hydroxide, a sodium alkoxide, a potassium alkoxide, a magnesium alkoxide, and an aluminum alkoxide.

20. The method of claim 19 , wherein the alkali catalyst is selected from an alkali hydroxide and an alkali alkoxide.

21. The method of claim 20 , wherein the alkali catalyst is selected from sodium hydroxide and sodium methoxide.

22. The method of claim 19 , wherein the mixture results from the transesterification of a triglyceride.

23. The method of claim 22 , wherein the transesterification product comprises a carboxylic acid ester and an alcohol.

24. The method of claim 23 , wherein the alcohol is selected from methanol and ethanol.

25. The method of claim 17 , wherein the mixture is selected from one or more of a product, an unreacted reactant, and a participant of the transesterification reaction.

26. A method for removing one or more chemicals after a reaction involving the transesterification of an ester, the method comprising:

providing a mixture resulting from the transesterification of the ester, wherein the mixture comprises an alkali catalyst, an alcohol, a biodiesel, and a glycerin, wherein the alkali catalyst is selected from sodium hydroxide and sodium alkoxide, and wherein the alcohol is selected from methanol and ethanol;

adding carbon dioxide to the mixture to convert the alkali catalyst into a solid phase selected from an alkali carbonate and an alkali bicarbonate; and

separating the solid phase from the mixture.

Assignments (3)
MERGER AND CHANGE OF NAME Recorded Sep 21, 2018
From: FIELD UPGRADING LIMITED; ENLIGHTEN INNOVATIONS INC.
To: ENLIGHTEN INNOVATIONS INC.
Reel/Frame 047586/0443 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 8, 2017
From: CERAMATEC, INC.
To: FIELD UPGRADING LIMITED
Reel/Frame 043788/0907 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 30, 2011
From: PENDLETON, JUSTIN; BHAVARAJU, SAI; DUFFEY, KEAN
To: CERAMATEC, INC.
Reel/Frame 026533/0882 →