GB2387390A

GB2387390A - Recovery of minor components from vegetable oils and fats

Info

Publication number: GB2387390A
Application number: GB0305427A
Authority: GB
Inventors: Ping Tou Gee
Original assignee: SUPERVITAMINS Sdn Bhd
Current assignee: SUPERVITAMINS Sdn Bhd
Priority date: 2000-12-14
Filing date: 2001-11-29
Publication date: 2003-10-15
Anticipated expiration: 2021-11-29
Also published as: GB2387384A; GB0305427D0; GB0305425D0; GB2387390B; GB2387384B

Abstract

A process for the production of free fatty acids, tocotrienol, sterol and diglyceride from crude vegetable oil and fat, the process comprising the steps of: <SL> <LI>a) removal of polar components from the crude vegetable oil and fat using a lower alkyl alcohol or a lower alkyl alcohol-water mixture, wherein lower alkyl means alkyl groups having 1 to 5 carbon atoms; <LI>b) short path distillation of the alcohol extract after alcohol removal under vacuum to produce free fatty acids; <LI>c) further short path distillation of the residue obtained from step (b) under vacuum to produce tocotrienol and sterol as distillate and diglyceride as residue; and <LI>d) further short path distillation of the residue obtained from step (c) under vacuum to produce diglyceride concentrate. </SL>

Description

RECOVERY OF MINOR COMPONENTS AND REFINING OF VEGETABLE

OILS AND FATS

Technical Field of the Invention

This invention relates to a process for the recovery of minor components and refining of 5 vegetable oils and fats from crude vegetable oils and fats, in particular, a process for the recovery of minor components and refining of vegetable oils and fats from seed oil, pulp oil and other vegetable matter.

Background of the Invention

10 Crude palm oil contains less than 5% of free fatty acid (FFA). The main fatty acids are palmitic acid and oleic acid. During fractionation, fatty acid is slightly concentrated in the palm olein. Crude palm oil contains 600-1000 ppm of tocotrienol/tocopherol mixture.

The tocotrienol presence in palm oil are y-tocotrienol, oc-tocopherol, atocotrienol and 8-

tocotrienol in an approximate ratio of 5:2:2:1. Tocotrienol is also enriched in the palm 15 olein during fractionation. Tocotrienol was claimed to be very effective in cholesterol lowering, preventing arteriosclerosis and stroke, inhibits breast cancer cells, protecting the skin against the effects of ultraviolet radiation and as powerful antioxidant.

Typical crude palm oil contains more than 4% of diglyceride. Diglyceride is considered 20 undesirable as it affects crystallization during fractionation. Based on long term human study on feeding of diglyceridesrich cooking oil, diglyceride was said to be able to reduce serum triglycerides, increased serum high density lipoprotein (HDL)-cholesterol and reduction in plasminogen activator inhibitor.

25 Crude palm oil contains about 500-700 ppm of carotene. The main carotene components are p-carotene and a-carotene. During fractionation, carotene is concentrated in the olein (liquid) fraction. Crude palm olein can contain up to 1500 ppm of carotene whereas crude palm stearin (the solid fraction) has much lower carotene (as low as less than 200 ppm). Consumption of a mixture of natural carotene was claimed to provide 30 protection towards free radical mediated degenerative diseases such as cancer and cardiovascular diseases. It was also claimed that a-carotene but not p-carotene inhibited liver carcinogenesis. It was also claimed that intake of palm carotene inhibits skin peroxidation induced by ultraviolet radiation.

There are patents describing the production of refined red palm oil from crude palm oil.

These include U.S. Patent No. 5932261 and Australian Patent Application No. P18770/88. All these patents involved molecular distillation of palm oil at relatively 5 high temperature to remove the fatty acid.

There are also patents describing the production of carotene concentrate from crude palm oil. These include U.S. Patent No. 5157132, 6072092, 5019668 and U.K Patent No. GB2160874A, GB2218989A and GB1515238. Again all these patents involved 10 pretreatment to the free fatty acid, molecular distillation and followed by the process of post treatment such as using absorbents.

This invention relates to the process of producing refined red oils and fats, carotene concentrate, distilled fatty acid, tocotrienol and sterol concentrate, and diglyceride from I 15 carotene-containing natural oils and fats and has particular but not exclusive application to the process of producing these products from crude palm oil and its fractionated products by first removing the polar components prior to transesterification and therefore no post-treatment is necessary after distillation.

20 This invention has many advantages. It can refine palm oil and palm oil fractionated products without destroying the carotene at a lower vacuum distillation temperature since the polar components including that of odoriferous materials and free fatty acid are removed by alcohol extraction prior to distillation. It also can refine crude palm oil or its fractions into the refined, bleached and deodorized (R.B.D) oils without using 25 degumming agent such as phosphoric acid and deodorized at a significantly lower temperature as most of the free fatty acid and odoriferous materials have been removed. I This invention also enables transesterification to be carried out without pre-esterification of free fatty acid. It also enables production of carotene concentrate without the need of 30 post-distillation treatment such as using adsorbent. As the polar components had been removed from the oil prior to transesterification, the transesterification reaction was carried out without interference from the unsaponifiable matter and carotene remained in the residue. The processes described in the present invention are simpler and cost

effective as compared to that described in other patents on carotene recovery from palm oil. This invention also enables the recovery of FFA, tocotrienol, tocopherol, sterol and diglyceride and other useful minor components of palm oil.

5 Summary of the Invention

The object of the present invention is to provide a process for the recovery of minor components and refining of vegetable oils and fats from crude vegetable oils and fats without destroying naturally occurring components in the crude vegetable oils and fats.

10 Accordingly, there is provided a process for the recovery of minor components and refining of vegetable oils and fats wherein said process is: A process for the recovery of minor components and refining of vegetable oils and fats without destroying naturally occurring components, said process comprising the steps of: a) removal of polar components from the crude vegetable oils and fats using lower alkyl 15 alcohol or any lower alkyl alcohol-water mixture; b) removal of alcohol from the product obtained in step (a) by distillation; c) addition of suitable quantity of bleaching earth to the product obtained in step (b) at normal bleaching temperature followed by filtration; and d) deodourization of the product obtained in step (c) at a low temperature.

This invention will be clearly understood and apparent with reference to the detailed description which follows.

Detailed Description of the Invention

25 The features and details of the invention, either as steps of the invention or as combinations of parts of the invention will now be described. It will be understood that the particular embodiments of the invention are shown by way of illustration and not as limitations of the invention. The principle features of the invention may be employed in various embodiments without departing from the scope of the invention.

30 Carotene is non-polar in nature. It is freely soluble in oils and fats. Its solubility in lower alkyl alcohol is low. Natural oils and fats consist mainly of triglyceride, which also has low solubility in lower alkyl alcohol such as methanol and ethanol. Oils and fats are soluble in n-propanol, isopropanol and other lower alkyl alcohol. Addition of water or a

mixture of these lower alcohol water mixtures can be used to form two phases in the presence of oils and fats.

By using polar solvent such as lower alkyl alcohol or lower alkyl alcoholwater mixture, 5 the polar components such as FFA, tocopherol, tocotrienol, sterol, triterpene alcohol, mono-glyceride, all-glyceride, glycolipid and phospholipid can be extracted out from oils and fats, remaining the non-polar components such as carotene, squalene and triglyceride. l The oil or fat after lower alkyl alcohol extraction can be subjected to washing with water.

10 Residual solvent and/or water can be vacuum distilled at a temperature less than 100 C without destroying tocopherol and tocotrienol in the methanol extract. The mixture of FFA, tocopherol, tocotrienol, sterol, triterpene alcohol, mono-glyceride and all-glyceride I can be used for their recovery.

15 A 1-litre crude palm olein of sample was vigorously stirred with methanol at oil to methanol ratios of 1:1, 1:2, 1:3 and 1:4. Table 1 summarizes the results Oil: MeOH Extraction stages FFA, % Carotene, Weight of ratio ppm MeOH extract, g Initial 4.30 873 1:1 After Is' extraction 2.56 870 25.3 1:1 After2nd extraction 1.67 875 18.5 1: 1 After 3r extraction 0.98 873 14.8 1.1 After 4th extraction 0.59 904 10.0 1. 1 After 5th extraction 0.33 889 7.8 1: 1 After 6'h extraction 0.21 908 7. 1 1:1 After 7 extraction 0.16 906 6.9 1:1 After 8'i' extraction 0. 097 898 5.0 I Initial 4.20 862 1:2 After is' extraction 1.82 864 41.2 1:2 After2nd extraction 0.73 875 22.6 1:2 After 3ru extraction 0. 32 902 15.2 1:2 After 4' extraction 0.17 895 12.0 1:2 After 5th extraction 0.076 896 8.7 Initial 4.26 857 1.3 After Is' extraction 1. 49 896 53.6 1 3 After2nd extraction 0.44 896 32.5

1:3 After 3rd extraction 0.17928 19.2 I:3 After 4'h extraction 0. 052937 14.2 _ Initial 4.22895 1:4 After ISt extraction 1.20918 34.6 .. 1:4 After2nU extraction 0.30940 21.4 1:4 After 3rd extraction 0.095 9.5 The solvent extraction can be carried out at room temperature (about 32 C) . It was observed that carotene content increases after removal of the polar materials. It is understood that other room temperatures can also be used. There is no advantage to carry 5 out the extraction at the methanol refluxing temperature or other temperature between room temperature and methanol refluxing temperature. At methanol refluxing temperature, more neutral oil (triglyceride) was extracted and the carotene content is lower than that of the starting material indicating some deterioration of carotene under those conditions. Table 2 summarizes the methanol extraction that was carried out at the 10 methanol refluxing temperature.

Oil: MeOH Extraction stages FFA, % Carotene, Weight of ratio ppm MeOH extract, g Initial 4.36 897 1:1 After I st extraction 2.64 864 27.0 1:1 After2n extraction 1.66 874 25.5 1:1 After 3rd extraction 0.96 861 12. 6 1:1 After 4th extraction 0.61 850 10.7 1:1 After 5'h extraction 0. 34 827 8.8 1:1 After 6' extraction 0.20 823 7.5 1:1 After in extraction 0. 12 815 _ 7.2 1:1 After 8t extraction 0.083 802 6.0 __ Initial 4.23 885 1:2 After lS' extraction 1.71 898 51.4 1:2 After2n extraction 0.75 871 29. 6 1:2 After 3r extraction 0.28 894 26.6 1:2 After 4tn extraction 0. 12 884 18.3 1:2 ARer 5t extraction 0.042 860 8.6 Initial 4.26 892 1:3 After lS' extraction 1.37 905 73.0 1:3 After2nd extraction 0. 40 896 44.1

I:3 After 3rd extraction 0.13 886 31.6 I:3 After 4th extraction 0. 038 880 17.0 Initial 4.18 904 I:4 After 1st extraction 1.02 900 40.2 1 4 After extraction 0.24 907 21.0 After 3rd extraction 0.071 864 12.2 It is understood that other polar solvents such as other lower alkyl alcohols or their water mixture can also be used as solvent to extract components such as free fatty acid, tocopherol, tocotrienol, sterol, triterpene alcohol, mono-glyceride and all-glyceride) from 5 natural oils and fats. Lower alkyl preferably refers to alkyl groups having between I and 5 carbon atoms, more preferably 1 to 4 carbon atoms.

For lower alkyl alcohol with three or more carbons, such as iso-propanol and n-propanol, addition of water is necessary to form two phases with the oil. Table 3 revealed the effect 10 of water content in isopropanol after the first extraction at room temperature, using the oil to solvent ratio of I:2. The addition of water at 5% volume to isopropanol is preferred over the higher water content.

Extraction solvent FFA, % Carotene, ppm 5% water in iso-propanol 1.25 896 10% water in iso-propanol 1.42 847 15% water in iso-propanol 1.57 825 20% water in iso-propanol 1.87 835 15 The carotene-containing oil after the methanol extraction still contains about 10% methanol. The methanol can be removed by vacuum distillation at a temperature not more than the 65 C (boiling point of methanol) and the product is refined red palm oil or refined red palm oil fractions such as refined red palm superolein, refined red palm olein and refined red palm stearin. It is understood that anti-oxidants, either natural or synthetic 20 in origin or a combination of both can be added to the red palm oil or its corresponding fractionated products. It is also understood that anti-oxidants, either natural or synthetic in origin or a combination of both can be added to the carotene containing oil before distillation of methanol.

- 7 The subsequent carotene-containing oil can be used directly for esterification. In a preferred embodiment, transesterification with 6 molar volume of methanol in the presence of 0.5% sodium hydroxide as catalyst is used. It is understood that acid 5 catalyzed esterification or transesterification with other bases such as sodium methoxide or potassium hydroxide or at other suitable amounts of methanol and/or catalyst can also be used. It is also understood that small amount of vegetable oil such as sunflower oil can be added into the carotene- containing oil prior to distillation or in the residue receiving vessels for collecting the carotene concentrate.

Transesterification process is monitored by high- resolution gas liquid chromatography using Restek Rtx 65TG column with hydrogen as carrier gas. Glycerol-rich layer can be phased separated and drained continuously or when the reaction is toward completion.

The reaction is complete when all the triglyceride and diglyceride peaks disappear in the 1 5 chromatogram.

The methyl ester layer is centrifuged, with or without addition of small quantity of water to remove small quantity of soap and methanol.

The methyl ester layer is then vacuum distilled. In a preferred embodiment, the methyl 20 ester is degassed in a thin film evaporator, and vacuum distilled less than 3 Pa and at less than 160 C in two stages of short path evaporator. It is understood that degassing can also be carried with short path evaporator or other suitable vacuum distillation unit. It is also understood that distillation of methyl ester can be carried out with different number of evaporator stages. Carotene concentrate is collected as residue.

Methanol in the glycerol layer is distilled at less than 1 00 C, preferably under vacuum of less than 20,000 Pa. Glycerol is distilled at less than 160 C under vacuum of 100 Pa. The methanol extract is distilled to remove the methanol. The residual methanol extract is then subjected to degassing and vacuum distillation in short path evaporators. FFA are 30 distilled first, followed by tocotrienols, tocopherol and sterols, and finally diglycerides. In a preferred embodiment, FFA are distilled at about 200 C under vacuum of 2 Pa, tocotrienol, tocopherol and sterol at less than 220 C under vacuum of 0.1 Pa, and diglyceride at 271 C under vacuum of 0.1 Pa.

After methanol removal, the oil after methanol extraction can be processed into R.B.D. oil by treatment with 0.5% of bleaching earth at 90 to 120 C under partial vacuum, filter and deodorized at 170 to 240 C under vacuum of 300 to 500 Pa. It is understood that higher 5 dosage of bleaching earth and/or higher deodorization temperature can also be carried out.

The oil refined using this process do not need degumming with phosphoric acid, uses less bleaching earth and deodorized at lower temperature as the process had already removed the fatty acid and odoriferous materials prior to refining.

10 After methanol removal, the oil after methanol extraction can be fractionated or further fractionated. Since most of the diglycerides and unsaponifiable matter have been removed prior to the fractionation process, the crystallization behavior is more predictable as compared to the conventional fractionation of palm oil.

15 Description of Preferred Embodiments

The present invention will now be further specifically described by the following I examples. All parts and percentages are by weight unless otherwise stated.

EXAMPLE I

20 Polar materials were extracted from 1 L of crude palm superolein (with 4.20% FFA, 862 ppm of carotene and 5.7% diglyceride) by adding 2 L of methanol and the mixture was stirred vigorously at room temperature for 5 minutes in a suitable container such as 5-L conical flask. The mixture was transferred into a 5-L separating funnel and allowed to settle into two phases. The lower oil phase was collected and placed into a 5-L conical 25 flask. The methanol layer was transferred into a 1-L evaporation flask and rotary evaporated at water bath temperature of 60 C under vacuum. The yield of methanol extract was 41.2 g, consisting of 59. 6% FFA, 1.2% of tocotrienols, tocopherol and sterols and 20.3% diglycerides.

30 The oil layer (the oil with 1.82% FFA and 864 ppm carotene) which contained about 10% of methanol in it was further added with 2 L of methanol. The second extraction process was repeated as described above. The yield of methanol extract was 22.6g, consisting of 48.0% FFA, 1.6% tocotrienols, tocopherol and sterols and 24.6% diglycerides.

- l The oil layer (the oil with 0.73% FFA and 875 ppm carotene) which contained about 10% of methanol in it was further added with 2 L of methanol. The third extraction process was repeated as described above. The yield of methanol extract was 15.2g, consisting of 5 26.1 % FFA, 2.0% tocotrienols, tocopherol and sterols and 36.4% diglycerides.

The oil layer (the oil with 0.32% FFA and 902 ppm carotene) which contained about 10% of methanol in it was further added with 2 L of methanol. The fourth extraction process was repeated as described above. The yield of methanol extract was 12.0g, consisting of 10 12.3% FFA, 1.6% tocotrienols, tocopherol and sterols and 34.6% diglycerides.

The oil layer (the oil with 0.17% FFA and 895 ppm carotene) which contained about 10% of methanol in it was further added with 2 L of methanol. The fifth and final extraction process was repeated as described above. The yield of methanol extract was 8.7g, 15 consisting of 5.3% FFA, 1.5% tocotrienols, tocopherol and sterols and 35.8% diglycerides. The oil layer was rotary evaporated. The red palm superolein contained 0.076% FFA and 896 ppm of carotene and 2.8% diglyceride. The red palm superolein can be further 20 subjected to thin film or short path evaporator to further remove traces of fatty acid and volatile matter.

EXAMPLE II

Polar materials were extracted from I L of crude palm oil (with 2.71% FFA, 577 ppm of 25 carotene and 4.1% diglycerides by adding 2 L of methanol and the mixture was stirred vigorously at 40 C for 5 minutes in a suitable container such as 5-L conical flask. The mixture was transferred into a 5-L separating funnel and allowed to settle into two phases.

The lower oil phase was collected and placed into a 5-L conical flask. The methanol layer was transferred into a 1-L evaporation flask and rotary evaporated at water bath 30 temperature of 60 C under vacuum. The yield of methanol extract was 29.3 g, consisting of 53.3% FFA, 1.2% of tocotrienols, tocopherol and sterols and 21.5% diglycerides.

The oil layer (the oil with 1.09% FFA and 599 ppm carotene) which contained about 10% of methanol in it was further added with 2 L of methanol. The second extraction process was repeated as described above. The yield of methanol extract was 19.2g, consisting of 37.5% FFA, 1.6% tocotrienols, tocopherol and sterols and 33.8% diglycerides.

The oil layer (the oil with 0.53% FFA and 599 ppm carotene) which contained about 10% of methanol in it was further added with 2 L of methanol. The third extraction process was repeated as described above. The yield of methanol extract was 15.1g, consisting of 20.9% FFA, I.4% tocotrienols, tocopherol and sterols and 33.7% diglycerides.

The oil layer (the oil with 0.20% FFA and 604 ppm carotene) which contained about 10% of methanol in it was further added with 2 L of methanol. The fourth extraction process was repeated as described above. The yield of methanol extract was 9.4g, consisting of I 9.3% FFA,1.3% tocotrienols, tocopherol and sterols and 34.8% diglycerides.

The oil layer (the oil with 0.09% FFA and 609 ppm carotene) which contained about 10% of methanol in it was further added with 2 L of methanol. The fifth and final extraction process was repeated as described above. The yield of methanol extract was 8.5g,; consisting of 5. % FFA, 1.4% tocotrienols, tocopherol and sterols and 35.9% t 20 diglycerides. The oil layer was rotary evaporated. The red palm oil contained 0.043% FFA and 604 ppm of carotene and 1.7% diglyceride. The red palm olein can be further subjected to thin film or short path evaporator to further remove traces of fatty acid and volatile matter.

25 EXAMPLE III

Polar materials were extracted from 539g of crude palm superolein (with 4. 17% FFA, 804 ppm of carotene and 4.6% diglycerides by adding 1 L of isopropanol added with 5% (v/v)! of water and the mixture was stirred vigorously at room temperature for 5 minutes in a suitable container such as 5-L conical flask. The mixture was transferred into a 5-L 30 separating funnel and allowed to settle into two phases. The lower oil phase was t collected and placed into a 5-L conical flask. The isopropanol-water layer was transferred into a l-L evaporation flask and rotary evaporated at water bath temperature of 70 C

under vacuum. The yield of isopropanol extract was 74.5g, consisting of 20.8% FFA, 0.7% tocotrienols, tocopherol and sterols and 16.8% diglycerides.

The oil layer (the oil with 2.23% FFA and 894 ppm carotene) which contained about 10% 5 of isopropanol/water in it was further added with I L of isopropanol added with 5 /O (v/v) water. The second extraction process was repeated as described above. The yield of isopropanol extract was 78.1g, consisting of 9.9% FFA, 0.5% tocotrienols, tocopherol and sterols and 11.3% diglycerides.

10 The oil layer (the oil with 0.94% FFA and 981 ppm carotene) which contained about 10% of isopropanol in it was further added with I L of isopropanol added with 5% (v/v) water.

The third extraction process was repeated as described above. The yield of isopropanol extract was 57.6g, consisting of 4,1% FFA, 0.3% tocotrienols, tocopherol and sterols and 7.2% diglycerides.

The oil layer (the oil with 0.39% FFA and 1064 ppm carotene) which contained about 10% of isopropanol/water in it was further added with I L of isopropanol added with 5% (v/v) water. The fourth extraction process was repeated as described above. The yield of isopropanol extract was 43. 2g, consisting of 1.3% FFA, 0.2% tocotrienols, tocopherol and 20 sterols and 4.7% diglycerides.

The oil layer (the oil with 0.12% FFA and 1138 ppm carotene) which contained about 10% of isopropanol/water in it was further added with I L of isopropanol with 5% (v/v) water. The fifth and final extraction process was repeated as described above. The yield 25 of isopropanol extract was 41.0g, consisting of 0.5% FFA, 0.1% tocotrienols, tocopherol and sterols and 3.1 % diglycerides.

The oil layer was rotary evaporated. The red palm superolein contained 0. 078% FFA, 1250 ppm of carotene and 0.3% diglyceride. The red palm superolein can be further 30 subjected to thin film or short path evaporator to further remove traces of fatty acid and volatile matter.

EXAMPLE 1V

Polar materials were extracted from 492g of crude palm superolein (with 4. 66% FFA, 820 ppm of carotene and 4.7% diglycerides by adding 1 L of 95% ethanol and the mixture was stirred vigorously at room temperature for 5 minutes in a suitable container such as 5-L I 5 conical flask. The mixture was transferred into a 5-L separating funnel and allowed to settle into two phases. The lower oil phase was collected and placed into a 5-L conical flask. The ethanol layer was transferred into a 1-L evaporation flask and rotary evaporated at water bath temperature of 70 C under vacuum. The yield of ethanol extract was 22.9g, consisting of 68.9% FFA, 1.2% of tocotrienols, tocopherol and sterols and 10 17.7% diglycerides.

The oil layer (the oil with 2.50% FFA and 852 ppm carotene) which contained about 10% ethanol in it was further added with 1 L of 95% ethanol. The second extraction process was repeated as described above. The yield of ethanol extract was 12.4g, consisting of 15 46.8% FFA,1.7% tocotrienols, tocopherol and sterols and 25.6% diglycerides.

The oil layer (the oil with 1.15% FFA and 863 ppm carotene) which contained about 10%; of ethanol in it was further added with 1 L of 95% ethanol. The third extraction process was repeated as described above. The yield of ethanol extract was 9.2g, consisting of 20 42.3% FFA,1.7% tocotrienols, tocopherol and sterols and 28.7% diglycerides.

The oil layer (the oil with 0.65% FFA and 867 ppm carotene) which contained about 10% of ethanol in it was further added with 1 L of 95% ethanol. The fourth extraction process was repeated as described above. The yield of ethanol extract was 7.0g, consisting of 25 29.3% FFA,1.8% tocotrienols, tocopherol and sterols and 31.0% diglycerides.

The oil layer (the oil with 0.30% FFA and 888 ppm carotene) which contained about 10% of ethanol in it was further added with 1 L of 95 % ethanol. The fifth extraction process was repeated as described above. The yield of ethanol extract was 7.3g, consisting of 30 19.0% FFA, 1.7% tocotrienols, tocopherol and sterols and 35.8% diglycerides.

The oil layer (the oil with 0.17% FFA and 862 ppm carotene) which contained about 10% of ethanol in it was further added with 1 L of 95% ethanol. The sixth extraction process

l was repeated as described above. The yield of ethanol extract was 5.4g, consisting of 9.9% FFA, 1.4% tocotrienols, tocopherol and sterols and 34. 0% diglycerides.

The oil layer (the oil with 0.12% FFA and 871 ppm carotene) which contained about 10% 5 of ethanol in it was further added with 1 L of 95% ethanol. The seventh and final extraction process was repeated as described above. The yield of ethanol extract was 4.7g, consisting of 3. 8% FFA, 1.5% tocotrienols, tocopherol and sterols and 39.3% diglycerides. 10 The oil layer was rotary evaporated. The red palm superolein contained 0.058% FFA, 854 ppm of carotene and 2.0% diglyceride. The red palm superolein can be further subjected to thin film or short path evaporator to further remove traces of fatty acid or volatile matter. 15 EXAMPLE V

The oil after final extraction was used for transesterification directly. 3.52kg of crude palm superolein (carotene content 763 ppm) extracted similar to Example I. After the final extraction, the oil was reacted with 1 L of methanol in the presence of 17.6g of sodium hydroxide. The reaction took place at the reflex temperature of methanol for 30 20 minutes. Gas chromatography revealed no trace of triglyceride or diglyceride, indicating that the reaction was completed. The mixture was transferred into a 5-L conical flask and allowed to settle. The lower glycerol layer was drained out. (0.82kg, containing about 54% methanol). The upper methyl ester layer was washed ten times with one volume of water. The yield of methyl ester was 3.49kg (99.1% yield). The carotene ester was also 25 763 ppm.

EXAMPLE VI

24 kg of carotene-containing methyl ester (carotene 763 ppm) was fed into KD6 short path evaporator at the rate of 4.8kg per hour, degasser at 100 Pa, 120 C, short path 30 evaporator at 0.8 Pa, 130 C, internal condenser at 12 C. Fatty acid methyl ester was collected as residue (95.8% yield) and carotene concentrate was collected as residue (4.3% yield, carotene content 1.56%).

EXAMPLE VII

170.5g of carotene-containing methyl ester (carotene 1.56%) was fed into KDLS short path evaporator at the rate of 602g per hour, short path evaporator at 6 Pa, 155 C, internal condenser at 20 C. Fatty acid methyl ester was collected as residue (81.6% yield) and S carotene concentrate was collected as residue 8 4 O field, carotene content 8.6%).

EXAMPLE VIII

4.1kg of methanol extract (after rotary evaporation of methanol) was degassed using a KDL5 short path evaporator at the rate of 973g per hour with evaporator at 110 C, 11700 10 Pa, internal condenser at 15 C and liquid nitrogen cold trap. The yield of volatile in the cold trap was 0. 8%, consisting of methanol and water. 3.7% of distillate, consisting of hydrocarbons and fatty acids were also obtained.

The degassed methanol extract was again fed into KDLS short path evaporator at the rate 15 of 955g per hour, short path evaporator at 2 Pa,195 C, internal condenser at 50 C. FFA was collected as distillate (48. 2% yield).

The residue (51.8% yield) was fed again into the KDLS short path evaporator at the rate of 955g per hour, short path evaporator at 0.1 Pa, 220 C, internal condenser at 55 C.

20 Tocopherol, tocotrienol, sterol and diglyceride were collected as distillate (10.5% yield).

The composition of the distillate were a-tocopherol 1.26%, a-tocotrienol 0.92%, y tocotrienol 2.27% and 6-tocotrienol 1.46%, campesterol 1.46%, stigmasterol 1.34% and 0-sitosterol 4.80%, diglyceride 61.8%.

25 The residue (89.5% yield) consists of diglyceride 61.72% and the balance were triglyceride, was fed again into the KDLS short path evaporator at the rate of 633g per hour, short path evaporator at 0.1 Pa, 271 C, internal condenser at 60 C. Diglyceride was collected as distillate (70.5% yield). The composition of the distillate was mainly diglyceride (84.6%) with the balance as triglyceride.

EXAMPLE IX

lkg of refined red superolein obtained similar to Example I was divided into 3 equal portions. 0, 0.3 and 0.5% of bleaching earth (Pure-Fro M85/20) were added into the three portions respectively. The samples were bleached at 1 05 C for 15 minutes under nitrogen 5 blanket, filtered through Whatman No. 1 filter paper, and steam distilled at 240 C for 60 minutes at 500 Pa vacuum. The reamed palm superolein were determined for Lovibond colour in 133.35mm (5/ inch) cell and the readings were 3.6R, 2. 8R and 2.6R respectively. 10 It should be understood that the preceding is merely a detailed description of certain

preferred embodiments. It therefore should be apparent to those skilled in the art that various modifications and equivalents can be made without departing from the spirit and scope of the invention. It is intended to encompass all such modifications within the scope of the appended claims.

All references, patents and patent publications that are recited in this application are incorporated in their entirety by reference.

Embodiments I. A process for the recovery of minor components and refining of vegetable oils and fats from crude vegetable oils and fats without destroying naturally occurring 5 components, said process comprising the steps of: a) removal of polar components from the crude vegetable oils and fats using lower alkyl alcohol or any lower alkyl alcohol-water mixture; b) removal of alcohol from the product obtained in step (a) by distillation; c) addition of suitable quantity of bleaching earth to the product obtained in step (b) at 10 normal bleaching temperature followed by filtration; and d) deodourization of the product obtained in step (c) at a low temperature.

2. A process for the recovery of minor components and refining of vegetable oils and fats from crude vegetable oils and fats as described in embodiment 1 wherein the addition I S of bleaching earth is carried out at a temperature of 90-1 20 C and the deodourization of the product obtained in step (c) is carried out at a temperature of 1 70-240 C.

3. A process for the recovery of minor components and refining of vegetable oils and fats from crude vegetable oils and fats as described in embodiment 1 wherein the removal 20 of polar components is achieved by using any suitable polar solvent mixture, for example, methanol-acetone mixture.

4. A process for the recovery of minor components and refining of vegetable oils and fats from crude vegetable oils and fats as described in embodiment 1 wherein the 25 vegetable oil and fat is seed oil.

5. A process for the recovery of minor components and refining of vegetable oils and fats from crude vegetable oils and fats as described in embodiment 4 wherein the seed oil is selected from the group consisting of soybean, cotton seed, sunflower seed, peanut, 30 rapeseed, palm kernel, coconut, linseed, sesame, grape seed, safflower seed, cocoa, corn, olive kernel, babassu, Borneo tallow(illipe), mowrah(illipe), walnut, rice bran, Shea, fulwah, oat, pumpkin, wheatgerm, hazelnut, almond, evening primrose, mango kernel, Sal and kokum.

6. A process for the recovery of minor components and refining of vegetable oils and fats from crude vegetable oils and fats as described in embodiment 1 wherein the vegetable oil and fat is pulp oil.

7. A process for the recovery of minor components and refining of vegetable oils and fats from crude vegetable oils and fats as described in embodiment 6 wherein the pulp oil is selected from the group consisting of palm, olive and avocado.

10 8. A process for the recovery of minor components from oil extracted from vegetable matter without destroying naturally occurring components, said process comprising the steps of: a) removal of polar components from extracted oil using lower alkyl alcohol or any lower alkyl alcohol-water mixture; 15 b) removal of alcohol from the product obtained in step (a) by distillation; c) addition of suitable quantity of bleaching earth to the product obtained in step (b) at normal bleaching temperature followed by filtration; and d) deodourization of the product obtained in step (c) at a low temperature.

20 9. A process for the recovery of minor components from oil extracted from vegetable matter as described in embodiment 8 wherein the minor component is carotene.

10. A process for the recovery of minor components from oil extracted from vegetable matter as described in embodiment 8 or 9 wherein the vegetable matter is selected from 25 the group consisting of algae, carrot and tomato.

1 1. A process for the recovery of methyl ester, glycerol and carotene concentrate from crude vegetable oils and fats using the process as described in anyone of embodiments 1 to 10 wherein the oils and fats after alcohol extraction from step (a) is transesterified with 30 a lower alkyl alcohol to give methyl ester, glycerol and carotene.

- 12. A process for the production of carotene concentrate as described in embodiment 11 wherein the vegetable oil is selected from the group consisting of palm oil, carrot oil, tomato oil or any other carotenecontaining natural vegetable oil and fat.

5 13. A process for the production of free fatty acid, tocotrienol, sterol and diglyceride from the alcohol extract of crude vegetable oils and fats using the product obtained from step (a) of embodiment 1, said process comprising the steps of: a) short path distillation of alcohol extract after alcohol removal under vacuum to produce free fatty acid; 10 b) further short path distillation of the residue obtained from step (a) under vacuum to I produce tocotrienol and sterol as distillate and diglyceride as residue; and c) further short path distillation of the residue obtained from step (b) under vacuum to produce diglyceride concentrate.

15 14. A refined vegetable oil and fat obtained using a process as described in anyone of embodiments 1 to 7.

I S. A process for the recovery of minor components and refining of vegetable oils and fats substantially as herein described.

20 t 16. A process for the production of free fatty acid, tocotrienol, sterol and diglyceride substantially as herein described.

17. A refined vegetable oil or fat obtained using a process substantially as herein 25 described.

Claims

1. A process for the production of free fatty acids, tocotrieno 1, sterol and diglyceride from crude vegetable oil and fat, the process comprising the steps of: S a) removal of polar components from the crude vegetable oil and fat using a lower alkyl alcohol or a lower alkyl alcohol-water mixture, wherein lower alkyl means alkyl groups having I to 5 carbon atoms; b) short path distillation of the alcohol extract after alcohol removal under vacuum to produce free fatty acids; 10 c) further short path distillation of the residue obtained from step (b) under vacuum to produce tocotrienol and sterol as distillate and diglyceride as residue; and d) further short path distillation of the residue obtained from step (c) under vacuum to produce diglyceride concentrate.

2. A process for the production of free fatty acid, tocotrienol, sterol and diglyceride from crude vegetable oil and fat substantially as herein described.