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Title:
A SYSTEM AND METHOD FOR THE RECOVERY OF AN OLEAGINOUS MATERIAL
Document Type and Number:
WIPO Patent Application WO/2006/058091
Kind Code:
A1
Abstract:
A method for the recovery of an oleaginous material from a feed stream that includes oleaginous material or an oleaginous material precursor, at least one emulsifier other than a fatty-acid salt, and water. In one embodiment, the method includes the steps of treating the feed stream to reduce the emulsification capacity of the emulsifier, and/or increase its hydrophilicity, and fractionating the treated feed stream into at least one aqueous phase and at least one lipophilic phase.

Inventors:
PURTLE IAN C (US)
EYAL AHARON M (IL)
VITNER ASHER (IL)
Application Number:
PCT/US2005/042496
Publication Date:
June 01, 2006
Filing Date:
November 22, 2005
Export Citation:
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Assignee:
CARGILL INC (US)
PURTLE IAN C (US)
EYAL AHARON M (IL)
VITNER ASHER (IL)
International Classes:
C11B13/00; B01D17/02; B01D17/04; C11B3/00; C11B13/02
Domestic Patent References:
WO2005077485A12005-08-25
Other References:
HAAS M J ET AL: "PRODUCTION OF FAME FROM ACID OIL, A BY-PRODUCT OF VEGETABLE OIL REFINING", JOURNAL OF THE AMERICAN OIL CHEMISTS' SOCIETY, AOCS PRESS, CHAMPAIGN, IL, US, vol. 80, no. 1, January 2003 (2003-01-01), pages 97 - 102, XP008049077, ISSN: 0003-021X
CLAUSEN K: "ENZYMATIC OIL-DEGUMMING BY A NOVEL MICROBIAL PHOSPHOLIPASE", EUROPEAN JOURNAL OF LIPID SCIENCE AND TECHNOLOGY, WILEY VCH VERLAG, WEINHEIM, DE, vol. 103, no. 6, June 2001 (2001-06-01), pages 333 - 340, XP001039221, ISSN: 1438-7697
HAAS M J ET AL: "SIMPLE, HIGH-EFFICIENCY SYNTHESIS OF FATTY ACIDS METHYL ESTERS FROM SOAPSTOCK", JOURNAL OF THE AMERICAN OIL CHEMISTS' SOCIETY, AOCS PRESS, CHAMPAIGN, IL, US, vol. 77, no. 4, April 2000 (2000-04-01), pages 373 - 379, XP008049188, ISSN: 0003-021X
HUI Y H ET AL: "A PRIMER ON OILS PROCESSING TECHNOLOGY", BAILEY'S INDUSTRIAL OIL AND FAT PRODUCTS. EDIBLE OIL AND FAT PRODUCTS : PROCESSING TECHNOLOGY, NEW YORK, NY : JOHN WILEY, US, vol. VOL. 4, 1996, pages 1 - 60, XP002213740, ISBN: 0-471-59428-8
PATENT ABSTRACTS OF JAPAN vol. 1999, no. 13 30 November 1999 (1999-11-30)
HAAS ET AL: "Combined Nonenzymatic-Enzymatic Method for the Synthesis of Simple Alkyl Fatty Acid Esters from Soapstock", JOURNAL OF THE AMERICAN OIL CHEMISTS' SOCIETY, AOCS PRESS, CHAMPAIGN, IL, US, vol. 73, no. 11, 1997, pages 1393 - 1401, XP002147540, ISSN: 0003-021X
Attorney, Agent or Firm:
Skarohlid, Gretchen (Incorporated Law 24, 15407 McGinty Roady Wes, Wayzata MN, US)
Download PDF:
Claims:
What is claimed is:
1. A method for the recovery of an oleaginous material from a feed stream comprising the oleaginous material or a precursor thereof, at least one emulsifier other than a fattyacid salt, and water, the treatment comprising: 5 (i) treating the feed stream to reduce the emulsification capacity of the emulsifier, increase its hydrophilicity, or reduce the emulsification capacity of the emulsifier and increase its hydrophilicity; and (ii) fractionating the treated feed stream into at least one aqueous o phase and at least one lipophilic phase.
2. The method of claim 1 , wherein a fraction of the aqueous phase is reused.
3. The method of claim 1 , wherein the oleaginous material is selected from a group comprising triglycerides, diglycerides, monoglycerides, fatty acids, phospholipids, lysophospholipids and their mixtures.
4. 5 4.
5. The method of claim 1 , wherein the step of treating the feed stream comprises a chemical modification, an enzymatic modification, or chemical and enzymatic modification.
6. The method of claim 1 , wherein the emulsifier is an ester, hydrolysable, or a hydrolysable ester.
7. o.
8. The method of claim 4, wherein the chemical modification, enzymatic modification, or chemical and enzymatic modification comprises at least one of hydrolysis of the emulsifier or transesterifying it.
9. The method of claim 1 , wherein the step of treating the feed stream is facilitated by at least one of temperature, a chemical catalyst, an enzyme, an 5 electrolyte, and combinations thereof.
10. The method of claim 1 , wherein the electrolyte comprises at least one of carboxylic acids, carboxylic acid salts, amino acid, amino acid salts, mineral salts, salts of potassium, salts of ammonium, salts of nitrate, salts of phosphate, and combinations thereof.
11. The method of claim 1 , wherein the emulsifier is a hydrolyzable emulsifier and comprises at least one of monoglycerides, diglycerides, phospholipids, non hydratable phosphatides, glycolipids, products of their partial hydrolysis, and mixtures thereof.
12. The method of claim 1 , further comprising hydrolyzing a sufficient amount of the emulsifier to facilitate phase separation of at least a fraction of the oleaginous material.
13. The method of claim 1 , further comprising hydrolyzing substantially all of the emulsifier.
14. The method of claim 1 , further comprising hydrolyzing substantially all of the emulsifier and substantially no triglycerides.
15. The method of claim 1 , further comprising hydrolyzing substantially all of the emulsifier and less than about 50 percent of the triglycerides.
16. The method of claim 1 , wherein the hydrolysis is conducted at a temperature of less than about 240 degrees Celsius.
17. The method of claim 1 , further comprising separating the remaining triglycerides from the lipophilic phase.
18. The method of claim 1 , wherein the separated lipophilic phase and/or the triglycerides are combined with crude vegetable oil.
19. The method of claim 1 , wherein the hydrolysis is conducted at a temperature between about 100 degrees Celsius and about 400 degrees Celsius.
20. The method of claim 1 , wherein the hydrolysis is conducted at a temperature between about 160 degrees Celsius and about 300 degrees Celsius.
21. The method of claim 1 , wherein the emulsifier and the triglycerides are both hydrolyzed.
22. The method of claim 1 , wherein at least a fraction of the triglycerides is hydrolyzed and the hydrolysis comprises forming fatty acids and glycerol and/or monoglycerides and/or diglycerides.
23. The method of claim 1 , further comprising separating fatty acids from the lipophilic phase after hydrolysis of the triglycerides, prior to hydrolysis or simultaneously with it.
24. The method of claim 1 , wherein the feed stream contains at least one salt of a fatty acid, further comprising a step of contacting with an acidic material to form free fatty acid.
25. The method of claim 1 , wherein the acidic material is selected from a group consisting of mineral acids, carboxylic acids, acidic oxides, acidic cation exchangers and acidic zeolites.
26. The method of claim 1 , further comprising a step of separating the formed fatty acid.
27. The method of claim 1 , wherein separating formed fatty acid uses at least one of distillation, adsorption, ionexchange and chromatography.
28. A method for the recovery of an oleaginous material from a feed stream comprising a triglyceride, an emulsifier other than a fattyacid salt, a fatty acid salt and water, comprising: (i) contacting the stream with an acidic material to form free fatty acid; (ii) reducing the em unification capacity of the emulsifier, and (iii) fractionating the stream into at least one aqueous phase and at least one lipophilic phase containing free fatty acid and a triglyceride.
29. The method of claim 26, further comprising the step of separating free fatty acid from the lipophilic phase of step (iii).
30. A method for the recovery of an oleaginous material from a feed stream comprising a triglyceride, an emulsifier other than a fattyacid salt, a fatty acid salt and water, comprising: (i) contacting the feed stream with an acidic material to form free fatty acids; (ii) separating at least a fraction of the free fatty acids to form separated free fatty acid and a fattyaciddepleted stream having the emulsifier; (iii) reducing the emulsification capacity of the emulsifier in the fattyacid depleted stream, and (iv) fractionating the fattyacid depleted stream into at least one aqueous phase and at least one lipophilic phase.
31. The method of claim 29, wherein a triglyceride is separated with the free fatty acids to form a mixture of free fatty acids and a triglyceride.
32. The method of claim 29, wherein contacting the stream with an acidic material is conducted prior to reducing the emulsification capacity, after it or simultaneously with it.
33. A method for refining a crude oil stream comprising: (i) degumming the crude oil stream to form degummed oil and gums comprising an emulsifier; (ii) treating the emulsifiercomprising gums to reduce the emulsification capacity of the emulsifier and/or to increase the hydrophilicity of the emulsifier, and (iii) fractionating the treated gums into at least one aqueous phase and at least one lipophilic phase.
34. A method for refining a crude oil stream comprising: (i) treating the stream with an alkali treatment to form alkalirefined oil and soapstock comprising an emulsifier other than a fatty acid; (ii) treating the soapstock to reduce the emulsification capacity of the emulsifier in the soapstock and/or to increase the hydrophilicity of the emulsifier; (iii) treating the soapstock by contacting with an acidic material to form free fatty acid; and (iv) fractionating the treated soapstock into at least one aqueous phase and at least one lipophilic phase.
35. A method for refining crude oil stream comprising: (i) degumming the crude oil to form degummed oil and gums comprising an emulsifier; (ii) treating the oil with an alkali treatment to form alkali refined oil, soapstock comprising an emulsifier other than a fatty acid salt and optionally also gums; (iii) contacting the soapstock with an acidic material to form free fatty acids; (iv) treating the soapstock and/or gums to reduce the emulsification capacity of the emulsifier and/or to increase the hydrophilicity of the emulsifier; and (v) fractionating at least one of the gums and the soapstock into at least one aqueous phase and at least one lipophilic phase.
36. A method for refining a crude oil stream comprising: (i) degumming the crude oil to form degummed oil and gums comprising an emulsifier; (ii) treating the oil with an alkali to form alkali refined oil, soapstock comprising an emulsifier other than a fatty acid salt and optionally also 5 gums; (iii) separating the gums and the soapstock to form a coproduct phase comprising at least a fraction of the emulsifier, at least a fraction of the gums and at least a fraction of the soapstock; (iv) treating the coproduct phase to reduce the emulsification capacity of 0 the emulsifier present in the coproduct phase and/or to increase the hydrophilicity of the emulsifier, and (v) fractionating the coproduct phase into at least one aqueous phase and at least one lipophilic phase.
37. The method of claim 34, further comprising contacting the coproduct phase 5 with an acidic compound prior to step (iv), after it or simultaneously with it to form free fatty acid.
38. The method of claim 35, wherein the crude oil stream is formed by contacting an oilseed with an organic solvent (e.g. hexane) followed by removing partially or substantially completely the solvent (e.g. by distillation) to form crude oil.
39. o.
40. The method of claim 36, wherein the crude oil stream is formed by contacting an oilseed with an organic solvent (e.g. hexane) and wherein at least a fraction (e.g. about 10% to about 100% by weight) of the solvent is present during the degumming and/or during the alkali treatment and/or during the reducing the emulsifying capacity and/or the increasing of the hydrophilicity of the emulsifier 5 and/or contacting with an acidic compound and/or fractionating.
41. The method of claim 36, wherein the solvent is separated (e.g. by distillation) from the degummed oil, from the alkalitreated oil or from the degummed and alkalitreated oil.
42. The method of claim 36, wherein the emulsifier is a phospholipid or is derived from a phospholipid and the treatment is catalyzed by an enzyme (e.g. phospholipase).
43. The method of claim 36, wherein the phospholipase catalyzes hydrolysis either of the phospholipids fatty acid or both, catalyzes transesterification of either of the phospholipids fatty acid or both or converts the phospholipid to triglyceride by transesterification.
44. The method of claim 36, wherein the enzyme is suited or adjusted for organic phases.
45. The method of claim 36, wherein the enzyme is modified by contact with a surfactant.
46. The method of claim 36, wherein the enzyme is immobilized on a solid carrier.
47. The method of claim 36, wherein the treated stream is moving respective to an immobilized enzyme.
48. The method of claim 36, further comprising the production of fatty acid esters by reacting at least one of separated oleaginous material, separated fatty acids and separated triglycerides with an alkanol or with an ester.
49. The method of claim 36, wherein the alkanol is of four carbon atoms or less.
50. The method of claim 36, further comprising the production of biodiesel by reacting at least one of separated oleaginous material, separated fatty acids and separated triglycerides with methanol or with a methyl ester.
51. The method of claim 36, further comprising the step of treating the separated aqueous phase for recovering at least one watersoluble component.
52. The method of claim 36, wherein the watersoluble component is a product of hydrolyzing at least one of triglycerides, diglycerides, monoglycerides, phospholipids, nonhydratable phosphatides, phosphatides and lyso phospholipids.
53. The method of claim 36, wherein at least one of separated oleaginous material, separated fatty acids and separated triglycerides is used in animal feed.
54. The method of claim 36, wherein at least one of separated oleaginous material, separated fatty acids and separated triglycerides is used for energy.
Description:
A SYSTEM AND METHOD FOR THE RECOVERY OF AN OLEAGINOUS MATERIAL

CROSS-REFERENCE TO RELATED APPLICATIONS

The following patent application is cross-referenced and hereby incorporated by reference in its entirety: U.S. Patent Application No. 60/543,062 titled "EFFLUENT TREATMENT SYSTEM" filed February 9, 2004. This application claims the benefit of U.S. Provisional Application No. 60/630,017 filed November 22, 2004, which is incorporated herein by reference in its entirety.

FIELD OF THE INVENTION The present invention generally relates to a system and method for the recovery of an oleaginous material. The present invention more particularly relates to an oil recovery system and method. The present invention more particularly relates to recovering from gums and soapstocks components such as oil, free fatty acids and products of phospholipids hydrolysis.

BACKGROUND OF THE INVENTION

In the conventional oil degumming process, water or steam (e.g. 1% water for soybean oil) is added to hot crude oil (~70C). As a result, a gum layer is formed (e.g. after contact time of ~5min.) and separated, e.g. by centrifugation. The thus degummed oil still contains phosphatides named non-hydratable phosphatides (NHP). Those NHP are removed in the alkali refining operation and end up in the soapstock.

Soapstock is the product of fatty acids removal from oil by treatment with an alkaline solution. Soapstock is formed and removed by centrifugation. Typically, neutral oil (triglycerides) is entrained in the recovered soapstock. An alternative to the conventional alkali treatment is removal of fatty acids by distillation (physical refining).

The preferred conventional practice is to recover value from soapstock by acidulation to liberate free fatty acids. If allowed to settle, the acidified soapstock breaks into three layers. The bottom layer is an acidic aqueous solution, which can be pumped off. The top layer contains the desired fatty acids and neutral oil. The middle layer, which is an emulsified sludge material, semi-solid, contains primarily gums, water and a substantial amount of desired fatty acids and neutral oil (its oleaginous material concentration is about 12%). In commercial soapstock acidulation processes, the sludge material is commonly retained with the fatty material initially. The sludge material is subsequently removed from the fatty layer by settling.

Aqueous solution separated from soapstock contains about 2.5-15% dissolved solids. Those include sulfuric acid and sodium sulfate (in cases where a sodium base was used in the alkali treatment and sulfuric acid in acidulation), glycerol, inositol phosphate and carbohydrates.

Known systems and methods for recovering from gums and soapstocks components such as oil, free fatty acids and products of phospholipids hydrolysis have several disadvantages including the use of flammable solvents, high-cost equipments, large amounts of water to be evaporated, etc. Accordingly, there is a need for an oil recovery system and method that provides for the relatively efficient recovery from gums and soapstocks of components such as oil, free fatty acids and products of phospholipids hydrolysis, commonly referred to as oleaginous material. It would be advantageous to provide a system and method for the recovery of an oleaginous material filling any one or more of these needs or having other advantageous features.

SUMMARY OF THE INVENTION

The present invention is directed to a method for the recovery of an oleaginous material (e.g. oil) from a feed stream that includes the oleaginous material or a precursor thereof, at least one emulsifier other than a fatty-acid salt, and water. In one embodiment, the method includes the steps of treating the feed stream to reduce the emulsification capacity of the emulsifier and/or to increase its

hydrophilicity, and fractionating the treated feed stream into at least one aqueous phase and at least one lipophilic phase.

In another embodiment, the present invention is directed to a method for the recovery of an oleaginous material from a feed stream that includes a triglyceride, an emulsifier other than a fatty-acid salt, a fatty acid salt and water. In one instance, the method includes contacting the stream with an acidic material to form free fatty acid, reducing the emulsification capacity of the emulsifier, and fractionating the stream into at least one aqueous phase and at least one lipophilic phase containing free fatty acid and a triglyceride.

The present invention can also be directed to a method for the recovery of an oleaginous material from a feed stream comprising a triglyceride, an emulsifier other than a fatty-acid salt, a fatty acid salt and water, that includes the steps of contacting the feed stream with an acidic material to form free fatty acids, separating at least a fraction of the free fatty acids to form separated free fatty acid and a fatty-acid-depleted stream having the emulsifier, reducing the emulsification capacity of the emulsifier in the fatty-acid depleted stream, and fractionating the fatty-acid depleted stream into at least one aqueous phase and at least one lipophilic phase.

In yet another embodiment, the present invention is directed to a method for refining a crude oil stream that includes the steps of degumming the crude oil stream to form degummed oil and gums comprising an emulsifier, treating the emulsifier-comprising gums to reduce the emulsification capacity of the emulsifier and/or to increase the hydrophilicity of the emulsifier, and fractionating the treated gums into at least one aqueous phase and at least one lipophilic phase.

Alternatively, the present invention can be directed to a method for refining a crude oil stream that includes the steps of treating the stream with an alkali treatment to form alkali-refined oil and soapstock comprising an emulsifier other than a fatty acid, treating the soapstock to reduce the emulsification capacity of the emulsifier in the soapstock and/or to increase the hydrophilicity of the emulsifier, treating the soapstock by contacting with an acidic material to form free

fatty acid, and fractionating the treated soapstock into at least one aqueous phase and at least one lipophilic phase.

In another instance, the present invention is directed to a method for refining crude oil stream that includes the steps of degumming the crude oil to form degummed oil and gums comprising an emulsifier, treating the oil with an alkali treatment to form alkali refined oil, soapstock comprising an emulsifier other than a fatty acid salt and optionally also gums, contacting the soapstock with an acidic material to form free fatty acids, treating the soapstock and/or gums to reduce the emulsification capacity of the emulsifier and/or to increase the hydrophilicity of the emulsifier; and fractionating at least one of the gums and the soapstock into at least one aqueous phase and at least one lipophilic phase.

In still another embodiment, the present invention is directed to a method for refining a crude oil stream that includes the steps of degumming the crude oil to form degummed oil and gums comprising an emulsifier, treating the oil with an alkali to form alkali refined oil, soapstock comprising an emulsifier other than a fatty acid salt and optionally also gums, separating the gums and the soapstock to form a co-product phase comprising at least a fraction of the emulsifier, at least a fraction of the gums and at least a fraction of the soapstock, treating the co- product phase to reduce the emulsification capacity of the emulsifier present in the co-product phase and/or to increase the hydrophilicity of the emulsifier, and fractionating the co-product phase into at least one aqueous phase and at least one lipophilic phase.

DETAILED DESCRIPTION OF THE PREFERRED AND OTHER EXEMPLARY EMBODIMENTS A system and method for the recovery of an oleaginous material relates to the recovery of an oleaginous material from a feed stream containing the oleaginous material or a precursor thereof, an emulsifier other than a fatty-acid salt, and water.

According to a preferred embodiment, the process comprises the steps of: (a) treatment that reduces the emulsification capacity of the emulsifier, and/or

increases its hydrophilicity and (b) fractionating into at least one aqueous phase and at least one lipophilic phase.

Oleaginous materials to be recovered according to the process include fatty acids and oil (neutral oil, triglycerides) according to a preferred embodiment. Feed streams suitable for treatment may result from various sources, including byproducts of oil refining such as gums, containing hydrated phospholipids and oil, and soapstocks containing fatty acid salts and oil according to any preferred or alternative embodiments. Other fatty-acid-salt containing and/or gums containing feed streams are also suitable for treatment if containing at least one emulsifier that is not a fatty acid salt. According to a preferred embodiment, the feed stream contains a solvent, e.g. hexane.

According to a preferred embodiment, in cases where the feed stream contains fatty acid salts, the process comprises an additional step of acidulation by contacting with an acidic material with acidity similar to that of the fatty acids or stronger.

In a preferred embodiment, such feed stream is a soapstock formed in the process of alkali refining of crude oil, wherein fatty acids are removed from crude oil as their salt. The alkali treatment is conducted after degumming or simultaneously with it, according to a preferred embodiment. Typically those are salts of alkaline metals such as sodium or potassium, but could also be salts of other metals, such as alkaline earth metals, and also salts of ammonia and of organic bases. Fatty acid salts are emulsifiers. According to a preferred embodiment, the stream to be treated contains, in addition, at least one other emulsifier, such as phospholipid, phosphatidic acid, non-hydratable phosphatide, a product of their hydrolysis, mono- and di-glyceride, glycolipid, etc. In many cases, that other emulsifier also results from the crude oil. The stream may also contain other fatty material, e.g. oil entrained in soapstock.

Acidulation is done by contacting with an acidic material, which is of acid strength similar to that of fatty acids or stronger, i.e. materials with pKa < 7, more preferably <5. That acidic material is at least partially in its free acid form

according to a particularly preferred embodiment. Both mineral and organic acids are suitable. Acidic oxides, such as SO2, acidic anion exchanges and acidic zeolites are also suitable. According to a preferred embodiment, the amount of acid used is similar to that of fatty acid salt in the treated stream or greater.

According to another preferred embodiment, the feed stream to be treated is obtained in the process of crude oil degumming.

Such stream, referred to as gums or crude lecithin, contains phospholipids, water and optionally also oil (neutral oil, triglycerides). According to another preferred embodiment, the feed stream to be treated is obtained in a combined or sequential degumming and alkali treatment or is formed by combining gums and soapstock.

According to a preferred embodiment, the stream to be treated contains a solvent. According to another preferred embodiment, the feed stream is obtained in treating crude oil, which is formed by contacting an oilseed (e.g. soybean, canola, sunflower, corn) with an organic solvent (e.g. hexane) followed by removing partially or substantially completely the solvent (e.g. by distillation) to form crude oil. According to a preferred embodiment, at least a fraction (e.g. about 10% to about 100% by weight) of the solvent is present during the degumming and/or during the alkali treatment and/or during the reducing the emulsifying capacity and/or the increasing of the hydrophilicity of the emulsifier and/or contacting with an acidic compound and/or fractionating.

According to a preferred embodiment, reducing the emulsifying capacity of the emulsifier is facilitated by at least one of temperature, a chemical catalyst, an enzyme, an electrolyte, and combinations thereof. According to a preferred embodiment, the electrolyte comprises at least one of carboxylic acids, carboxylic acid salts, amino acid, amino acid salts, mineral salts, salts of potassium, salts of ammonium, salts of nitrate, salts of phosphate, and combinations thereof.

Various methods could be used for the chemical or enzymatic modification of the non-fatty acid-salt emulsifier, e.g. ones that chemically modify its hydrophobic

end, ones that chemically modify its hydrophilic end, ones that detach or replace a hydrophilic fraction of it and ones that detach or replace a hydrophobic fraction of it according to alternative embodiments. Typically, such emulsifier is an ester or an ether and such detachment could be achieved by hydrolysis. Alternatively, 5 replacement is conducted by trans-esterification. Optionally, the hydrolysis is conducted at elevated temperature, preferably higher than about 100C, more preferably between about 100C and about 400C, most preferably between about 16OC and about 300C. According to a preferred embodiment, the reaction is conducted under super-atmospheric pressure. A suitable catalyst could be used. o Such catalysts include a chemical one or a biological one, e.g. an enzyme such as phospholipase. Catalyzed hydrolysis processes may be conducted at temperatures lower than non-catalyzed hydrolysis processes, particularly if enzymatically catalyzed.

According to a preferred embodiment an enzyme is used to facilitate reducing the s emulsifying capacity of the emulsifier and/or to increase its hydrophilicity.

According to a preferred embodiment the used enzyme is suited or adjusted for operation in an organic medium. According to another preferred embodiment, the enzyme is immobilized on a solid carrier. According to a preferred embodiment, the treated feed stream is moving respectively to an immobilized enzyme.

o In cases of emulsifiers containing more than one ester or ether bond in the molecule, it may be sufficient to hydrolyze or trans-esterify only one of those in order to form a product that is oil soluble and a product that is water soluble. Thus, in those cases where the emulsifier is a phospholipid, hydrolysis of the ester function in position 1 or 2 forms a lysophospholipid, which is water soluble, and a 5 fatty acid that is oil soluble. On the other hand, hydrolysis of the ester bond between the glycerol and the phosphate or that between the phosphate and the bound alkanol (e.g. choline, ethanolamine, serine or inositol) forms a small hydrophilic hydrolysis product and a larger, oil soluble product, e.g. phosphatidic acid. In some other cases, hydrolysis or trans-esterification of more than one o bond is preferred. According to still another preferred embodiment, one of the bonds on an emulsifier is hydrolyzed and another one is trans-esterified.

In those cases where hydrolysis or trans-esterification is used for the chemical modification of the emulsifier, the reaction may be selective to the emulsifier or non-selective so that both the emulsifier and oil present in the treated stream are reacted. Selective hydrolysis is e.g. an enzymatically catalyzed one. In non- enzymatically catalyzed hydrolysis, lower hydrolysis temperatures prefer the hydrolysis of phospholipids over the hydrolysis of oil. In cases where selective non-enzymatic hydrolysis is desired, the reaction is preferably conducted at a temperature of below about 240C.

The reduction in the emulsifying capacity may facilitate fractionation and increase the recovery yield in that step. The fractionation step may be a gravimetric fractionation, e.g. settling or centrifugation. Other fractionation methods are suitable too, e.g. solvent extraction and distillation according to alternative embodiments.

The fractionation step forms an aqueous solution. In cases where an acidulation step was conducted, the aqueous phase contains, among other components, the salt of the base used in the alkaline refining step and the acid used in the acidulation step.

The fractionation step also forms a lipophilic phase. That phase contains free fatty acids liberated from the fatty acid salts and free fatty acids formed in the hydrolysis step. In case of selective hydrolysis, those are mainly fatty acids detached from the emulsifier, while in case of non-selective hydrolysis, fatty acids could result also from hydrolysis of triglycerides. In case of selective hydrolysis, the lipophilic phase may also contain oil. The fatty acids in the lipophilic phase could be used for various applications, such as in animal feed and for the production of fatty acids esters, e.g. methyl ester to be used as biodiesel. If the lipophilic phase contains high proportion of oil, it could be combined with the partially refined oil at a suitable step of the refining and increase thereby the oil recovery yield. Alternatively, the free fatty acids are separated from the oil in the lipophilic phase, e.g. by distillation, preferably to form a stream of free fatty acids

and a stream of concentrated oil. Such concentrated oil can be combined with crude or partially refined oil and increase thereby the oil recovery yield.

In some cases, there may be a preference for repeating a step of the process. That is particularly true for the fractionation step. A fractionation step may be required after the chemical modification or simultaneously with it.

In processes involving an acidulation step, the process may be conducted in various sequences and in some cases also simultaneously. There is also the option of adding other streams or reagents at various stages of the process according to an alternative embodiment. For example, the chemical modification is conducted first, followed by acidulation and fractionation. Alternatively, acidulation is conducted first, followed by the chemical modification and fractionation. Conducting acidulation simultaneously with chemical modification is also an option. Still another option is acidulation first, followed by separation of the aqueous phase, and then chemical modification and fractionation. Chemical modification could also be conducted on the sludge formed by acidulation followed by separation of both an aqueous phase and a lipophilic phase. Gums, e.g. those formed in crude oil degumming, could be added at any of the steps, preferably prior to the chemical modification one.

According to a preferred embodiment, compounds present in the treated stream or formed during hydrolysis - e.g. choline, serine, glycerol or lysolecithin - are separated and optionally purified. Such separation is preferably conducted in cases where an aqueous phase is separated after acidulation and prior to the chemical modification or after it.

According to another preferred embodiment, the chemical modification for reducing the emulsifier capacity is conducted by a reaction with a hydrophilic part of the emulsifier. An example for such reaction is esterification of the hydroxyl group in diglyceride to form a triglyceride, preferably with a fatty acid present in the treated stream. Alternatively, the hydrophilic part is replaced by a lipophilic one, as in the case of trans-esterification wherein fatty acid replaces the phosphate ester on phospholipids.

While the preferred and other exemplary embodiments described in this disclosure are presently preferred, it should be understood that these embodiments are offered by way of example only. The invention is not limited to a particular embodiment, but extends to various modifications, combinations, and permutations.