IP Library Granted Patent US 7,560,579
Granted Patent B2
US 7,560,579 · App. 10/564,143 · Granted Jul 14, 2009

Process for preparing purified fatty acids

Assignee: Oleon N.V.
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Quick Facts
Patent No.
US 7,560,579
App. No.
10/564,143
Granted
Jul 14, 2009
Kind
B2
Abstract

The present invention relates to a process for preparing fatty acids derived from oils and/pr fats with a phosphorus content below 200 ppm in good yield and with good color and color stability, which process comprises the steps of (A) hydrolytic splitting of degummed oils and/or fats, (B) at least one thermal pre-treatment of a composition comprising crude fatty acids, and (C) high vacuum distillation of the thermally pre-treated composition comprising crude fatty acids.

Claims (30)

1. A process for preparing one or more purified fatty acids, said process consisting essentially of:

(A) hydrolytic splitting of one or more oils and/or fats with a phosphorus content below 200 ppm and separating a composition comprising crude fatty acids,

(B) heat-treating the composition obtained by step (A) in a thermal pre-treatment unit to provide a composition of crude fatty acids comprising at least 80% by weight (wt %) of free fatty acids, and

(C) distilling the heat-treated composition obtained by step (B) in a high vacuum distillation unit to obtain a composition of purified fatty acids comprising below 0.5% by weight of monoglyceride,

wherein the composition that is obtained by the thermal pre-treatment step (B) comprises less monoglycerides than the crude fatty acids obtained by step (A), and with the proviso that the hydrolytic splitting step (A) is not a saponification step.

2. The process of claim 1 wherein the heat-treatment in step (B) is conducted at a temperature of 150-280° C.

3. The process of claim 1 wherein in step (B) the composition is heat-treated in a continuously running thermal pre-treatment unit.

4. The process of claim 3 wherein both the heat-treating and the distillation step are conducted in a continuous fashion.

5. The process of claim 1 wherein the crude fatty acids that are obtained by the thermal pre-treatment step (B) are essentially free of glycerol and have an acid value of at least 150 mg/kg KOH.

6. The process of claim 1 wherein in step (C) the heat-treated composition of step (B) is distilled at a pressure within a range of 0.5-0.001 kPa and at a temperature of from 100 to 200° C.

7. The process of claim 1 wherein step (C) is conducted in a short path distillation unit.

8. The process of claim 1 wherein at least part of the residue that is obtained by the distillation step (C) is recycled to step (A).

9. The process of claim 1 wherein the oils and/or fats with a phosphorus content below 200 ppm that are subjected to the hydrolytic splitting in step (A) are selected from the group consisting of crude or degummed vegetable oils and fats, crude or degummed animal oils and fats, and acid oils, or mixtures thereof.

10. The process of claim 1 wherein one or more additives are used before, during, or after the thermal pre-treatment step (B), but in any case after the hydrolytic splitting step (A) and prior to the distillation step (C), said additives being effective for the removal of color bodies.

11. The process of claim 2 wherein the heat-treatment in step (B) is conducted at a temperature of 200-250° C.

12. The process of claim 11 wherein the heat-treatment in step (B) is conducted at a temperature of about 225° C.

13. The process of claim 3 wherein in Step (B) the composition is heat-treated in a continuously running thermal pre-treatment unit wherein the components of the composition have a residence time distribution of 0.7-1.5.

14. The process of claim 3 wherein the heat-treating step, the distillation step and the splitting process are conducted in a continuous fashion.

15. The process of claim 1 wherein said composition of crude fatty acids comprises at least 85% by weight (wt %) of free fatty acids.

16. The process of claim 1 wherein said composition of crude fatty acids comprises at least 90% by weight (wt %) of free fatty acids.

17. The process of claim 1 wherein said composition of crude fatty acids comprises at least 93% by weight (wt %) of free fatty acids.

18. The process of claim 1 wherein in step (C) the heat-treated composition of step (B) is distilled at a pressure in the range of 0.1 to 0.001 kPa and a temperature of from 120 to 180° C.

19. The process of claim 9 wherein the oils and/or fats with a phosphorus content below 200 ppm that are subjected to the hydrolytic splitting in step (A) are selected from selected from crude or degummed vegetable oils and fats, or mixtures thereof.

20. The process of claim 9 wherein the oils and/or fats with a phosphorus content below 200 ppm that are subjected to the hydrolytic splitting in step (A) are selected from selected from crude or degummed vegetable oils and fats that, after hydrolytic splitting of said oils and/or fats, provide saturated or unsaturated, optionally hydroxy containing, crude fatty acids with 6 to 24 carbon atoms, or mixtures thereof.

21. The process of claim 1 wherein in step (C) the heat-treated composition of step (B) is distilled at a pressure within the range of 0.1 to 0.001 kPa and at a temperature of from 120 to 180° C.

22. A process for preparing one or more purified fatty acids, said process consisting essentially of:

(A) hydrolytic splitting of one or more oils and/or fats with a phosphorus content below 200 ppm and separating a composition comprising crude fatty acids,

(B) heat-treating the composition obtained by step (A) in a thermal pre-treatment unit to provide a composition of crude fatty acids comprising at least 80% by weight (wt%) of free fatty acids, and

(C) distilling the heat-treated composition obtained by step (B) in a high vacuum distillation unit to obtain a composition of purified fatty acids comprising below 0.5% by weight of monoglyceride,

wherein the composition that is obtained by the thermal pre-treatment step (B) comprises less monoglycerides than the crude fatty acids obtained by step (A), and with the proviso that the hydrolytic splitting step (A) is not a saponification step, and wherein one or more additives are used before, during, or after the thermal pre-treatment step (B), but in any case after the hydrolytic splitting step (A) and prior to the distillation step (C), said additives being effective for the removal of color bodies.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 6, 2007
From: AKZO NOBEL N.V.
To: OLEON N.V.
Reel/Frame 019806/0072 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 21, 2006
From: TE BAAY, FRANZ-JOSEF; RIEMENSPERGER, HOLGER; MENSINK, INGO
To: AKZO NOBEL N.V.
Reel/Frame 017337/0226 →
Priority Claims (1)
EP 03077167 · Jul 10, 2003 · regional
Continuity (2)
Provisional Application 6050293600 · Sep 16, 2003
Related Publication 20060167291A1 · Jul 27, 2006