IMMOBILIZED ESTERIFICATION CATALYSTS FOR PRODUCING FATTY ACID ALKYL ESTERS

• US 20080289248A1
• Filed: 05/23/2007
• Published: 11/27/2008
• Est. Priority Date: 05/23/2007
• Status: Abandoned Application

• Current Assignee: Southern Illinois University (Board of Trustees of Southern Illinois University)
• Original Assignee: Southern Illinois University (Board of Trustees of Southern Illinois University)
• Inventors: Gao, Yong
• Application Number:
  US11/752,666
• Publication Number:
  US 20080289248A1
• Time in Patent Office: Days
• US Class Current: 44/308
• CPC Class Codes: C07C 67/03 by reacting an ester group with a hydroxy group
• CPC Class Codes: C07C 67/08 by reacting carboxylic acids or symmetrical anhydrides with the hydroxy or O-metal group of organic compounds
• CPC Class Codes: C07C 69/24 esterified with monohydroxylic compounds
• CPC Class Codes: C07C 69/52 Esters of acyclic unsaturated carboxylic acids having the esterified carboxyl group bound to an acyclic carbon atom
• CPC Class Codes: C10L 1/19 Esters ester radical containing compounds; ester ethers; carbonic acid esters C10L1/1802, C10L1/1805, C10L1/1808, C10L1/1811, C10L1/1814, C10L1/1817 take precedence
• CPC Class Codes: C11C 3/003 by esterification of fatty acids with alcohols C11C3/02 takes precedence
• CPC Class Codes: Y02E 50/10 Biofuels, e.g. bio-diesel

Abstract

Provided herein are processes for the production of biodiesel. In particular, provided is an esterification process in which an alcohol reacts with free fatty acids in a lipid material comprising free fatty acids and glycerides in the presence of an immobilized zirconium(IV) metal salt to form fatty acid alkyl esters. Also provided is combination process in which an esterification reaction converts the free fatty acids in a lipid material to fatty acid alkyl esters and a transesterification reaction converts the glycerides in the material to fatty acid alkyl esters.

Claims

1. A process for forming a fatty acid alkyl ester, the process comprising contacting a lipid material with an alcohol in the presence of a zirconium(IV) metal salt conjugated to a solid support and at a temperature from about 25°

C. to about 75°

C., whereby the alcohol reacts with a free fatty acid in the lipid material to form the fatty acid alkyl ester.

2. The process of claim 1, wherein the lipid material comprises free fatty acids and glycerides.

3. The process of claim 2, wherein the lipid material is selected from the group consisting of a vegetable oil, an animal fat, an algae oil, a food-based lipid waste, an industrial lipid waste, and a combination thereof.

4. The process of claim 3, wherein the lipid material is pretreated with a process selected from the group consisting of degumming, vacuum drying, steam distilling, bleaching, and a combination thereof.

5. The process of claim 1, wherein the alcohol is a short chain alcohol having from one carbon atom to about four carbon atoms.

6. The process of claim 5, wherein the short chain alcohol is selected from the group consisting of methanol, ethanol, propanol, isopropanol, butanol, isobutanol, and a combination thereof.

7. The process of claim 1, wherein the concentration of the alcohol is from about 1% to about 2000% by weight of the lipid material.

8. The process of claim 1, wherein the zirconium(IV) metal salt is a compound having a formula selected from the group consisting of ZrX₄, ZrOX₂.nH₂O, Zr(XO₄)₄, Zr(OR¹)₄, and Zr(OH)_m(OR¹)_p,

wherein:

X is a halogen atom selected from the group consisting of F, Cl, Br, and I;

n is an integer from 1 to about 10;

R¹ is an acyl group having from one carbon atom to about six carbon atoms or an alkyl group having from one carbon atom to about six carbon atoms; and

m and p are integers from 0 to 4, wherein the sum total of m and p is 4.

9. The process of claim 8, wherein the ZrX₄ or Zr(XO₄)₄ compound is coordinated with another ligand selected from the group consisting of tetrahydrofuran, N,N-dimethylformamide, and water.

10. The process of claim 8, wherein the zirconium(IV) metal salt is complexed with another metal salt selected from the group consisting of iron(III), tin(IV), gallium(III), and hafnium(IV).

11. The process of claim 1, wherein the solid support is selected from the group consisting of silicas, alumina, titania, carbondium, zirconia, activated charcoal, zeolites, clays, polymers, ceramics, activated carbon, porous metal supports, and a combination thereof.

12. The process of claim 1, wherein the zirconium(IV) metal salt is conjugated to the solid support by non-covalent bonding.

13. The process of claim 1, wherein the concentration of the zirconium(IV) metal salt is from about 0.2% to about 50% by weight of the lipid material.

14. The process of claim 1, wherein the concentration of the zirconium(IV) metal salt is from about 1% to about 20% by weight of the lipid material.

15. The process of claim 1, wherein the temperature is from about 50°

C. to about 70°

C.

16. The process of claim 1, wherein the temperature is about 65°

C.

17. The process of claim 1, wherein the process is conducted in a mode selected from the group consisting of batch, semi-continuous, and continuous.

18. The process of claim 1, wherein the lipid material is soybean oil, the alcohol is methanol, the zirconium(IV) metal salt is zirconium tetrachloride, the solid support is alumina, and the temperature is 65°

C.

19. The process of claim 1, wherein the conversion of free fatty acids to fatty acid alkyl esters is from about 13% to over 99%.

20. The process of claim 1, wherein the conversion of free fatty acids to fatty acid alkyl esters is at least about 90%.

21. A process for forming a biodiesel solution, the process comprising:

(a) contacting a lipid material with an alcohol in the presence of a first catalyst to form a first solution, wherein the lipid material comprises free fatty acids and glycerides, and the first catalyst comprises a zirconium(IV) metal salt; and

(b) contacting the first solution with a second catalyst selected from the group consisting of an N-heterocyclic carbene and an alkaline agent to form the biodiesel solution.

22. The process of claim 21, wherein step (a) is performed at a temperature from about 25°

C. to about 65°

C. and step (b) is performed at a temperature from about 25°

C. to about 40°

C.

23. The process of claim 21, wherein the lipid material is selected from the group consisting of a vegetable oil, an animal fat, an algae oil, a food-based lipid waste, an industrial lipid waste, and a combination thereof.

24. The process of claim 23, wherein the lipid material is pretreated with a method selected from the group consisting of degumming, vacuum drying, steam distilling, bleaching, and a combination thereof.

25. The process of claim 21, wherein the alcohol is a short chain alcohol having from one carbon atom to about four carbon atoms.

26. The process of claim 25, wherein the short chain alcohol is selected from the group consisting of methanol, ethanol, propanol, isopropanol, butanol, and isobutanol.

27. The process of claim 21, wherein the concentration of the alcohol is from about 1% to about 2000% by weight of the lipid material.

28. The process of claim 21, wherein the zirconium(IV) metal salt is a compound having a formula selected from the group consisting of ZrX₄, ZrOX₂.nH₂O, Zr(XO₄)₄, Zr(OR¹)₄, and Zr(OH)_m(OR¹)_p,

wherein:

X is a halogen atom selected from the group consisting of F, Cl, Br, and I;

n is an integer from 1 to 10;

R¹ is an acyl group having from one carbon atom to about six carbon atoms or an alkyl group having from one carbon atom to about six carbon atoms; and

m and p are integers from 0 to 4, wherein the sum total of m and p is 4.

29. The process of claim 28, wherein the ZrX₄ or Zr(XO₄)₄ compound is coordinated with another ligand selected from the group consisting of tetrahydrofuran, N,N-dimethylformamide, and water.

30. The process of claim 28, wherein the zirconium(IV) metal salt is complexed with another metal salt selected from the group consisting of iron(III), tin(IV), gallium(III), and hafnium(IV).

31. The process of claim 21, wherein the zirconium(IV) metal salt is conjugated to a solid support.

32. The process of claim 31, wherein the solid support is selected from the group consisting of silicas, alumina, titania, carbondium, zirconia, activated charcoal, zeolites, clays, polymers, ceramics, activated carbon, porous metal supports, and a combination thereof.

33. The process of claim 21, wherein the concentration of the zirconium(IV) metal salt is from about 1% to about 20% by weight of the lipid material.

34. The process of claim 21, wherein the N-heterocyclic carbene is a compound having a formula selected from the group consisting of (VI) and (VII):

wherein;

R² and R⁵ are independently selected from the group consisting of a hydrocarbyl group having from one carbon atom to about twelve carbon atoms and a substituted hydrocarbyl group having from one carbon atom to about twelve carbon atoms; and

R³ and R⁴ are independently selected from the group consisting of a hydrogen atom, a halogen atom, and a hydrocarbyl group having from one carbon atom to about six carbon atoms.

35. The process of claim 34, wherein the N-heterocyclic carbene is selected from the group consisting of 1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene, 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene, 1,3-diisopropylimidazol-2-ylidene, 1,3-bis(1-adamantyl)imidazol-2-ylidene, 1,3-dicyclohexylimidazol-2-ylidene, 1-butyl-3-methylimidzol-2-ylidene, 1,3-diisopropylimidzolin-2-ylidene, a metal derivative, a dimer thereof, and a combination thereof.

36. The process of claim 21, wherein the concentration of the N-heterocyclic carbene is about 0.02% to about 40% by weight of the lipid material.

37. The process of claim 21, wherein the N-heterocyclic carbene is conjugated to a solid support.

38. The process of claim 37, wherein the solid support is selected from the group consisting of silicas, alumina, titania, carbondium, zirconia, activated charcoal, zeolites, clays, polymers, ceramics, activated carbon, porous metal supports, and a combination thereof.

39. The process of claim 21, wherein the alkaline agent is selected from the group consisting of sodium hydroxide, potassium hydroxide, sodium methoxide₁ and potassium methoxide.

40. The process of claim 21, wherein the process is conducted in a mode selected from the group consisting of batch, semi-continuous, and continuous.

41. The process of claim 21, wherein the lipid material is soybean oil, the alcohol is methanol, the first catalyst is zirconium tetrachloride conjugated to alumina, and the second catalyst is 1-butyl-3-methylimidzol-2-ylidene.

42. The process of claim 21, wherein the yield of fatty acid alkyl esters is at least about 90%.

43. The process of claim 21, further comprising post-treating the biodiesel solution to remove reaction byproducts and/or impurities.