US2352883A - Production and purification of fatty oils - Google Patents
Production and purification of fatty oils Download PDFInfo
- Publication number
- US2352883A US2352883A US329303A US32930340A US2352883A US 2352883 A US2352883 A US 2352883A US 329303 A US329303 A US 329303A US 32930340 A US32930340 A US 32930340A US 2352883 A US2352883 A US 2352883A
- Authority
- US
- United States
- Prior art keywords
- oil
- solution
- solvent
- fatty
- precipitated
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B7/00—Separation of mixtures of fats or fatty oils into their constituents, e.g. saturated oils from unsaturated oils
- C11B7/0008—Separation of mixtures of fats or fatty oils into their constituents, e.g. saturated oils from unsaturated oils by differences of solubilities, e.g. by extraction, by separation from a solution by means of anti-solvents
Definitions
- This invention relates to the production and/or purification of fatty oils by a process involving solvent extraction and subsequent precipitation of the oil from the solution by cooling.
- One object of the invention is to provide an improved method of freeing the extracted fatty oil from the solvent. Another object of the invention is to provide a method of removing coloring matter, oxidized material, phosphatides, etc., from the fatty oil. Still another object is to provide a method for separating a fatty oil into various fractions of different degrees of unsaturation. Other objects of the invention will become apparent as the description thereof proceeds.
- oils which are derived from fatty oil containing raw material of vegetable or animal origin and which are regarded chemically to be the glycerol esters of high molecular weight aliphatic acids, either saturated or unsaturated and embrace the drying, semi-drying and non-drying oils.
- Fatty oils are, at present, produced from fatty oil containing raw materials of either vegetable or animal origin by cooking and allowing the oil to settle out; by pressing, or by solvent extraction.
- the present invention is concerned with improvements in the methods involving solvent extraction.
- a solvent process is considered tobe any process in which th fatty oil in the course of its preparation and/or purification is dissolved in solvents and subsequently separated therefrom.
- the oil is pressed from vegetable or animal material and subsequently dissolved in solvents it is considered a solvent process and the improved methods of the present invention are applicable thereto.
- fatty oil is recovered from a solvent solution by distillation of the solvent by the application of heat, vacuum, or both heat and vacuum.
- the recovered fatty oil contains any non-volatile impurities which may be contained in the solution whereas the solvent is recovered substantially pure.
- any solvent commonly used in extracting fatty oil from vegetable or animal oil containing raw materials and which does not solidify at the temperatures employed may be used in practicing the present inventions.
- Such solvents will include the coal tar derivatives, e. g. mineral spirits, petroleum derivatives, e. g. petroleum spirits, petroleum ether, etc., natural derivatives, e. g. turpentine, the alcohols, e. g. methyl, ethyl, isopropyl, propyl, etc., the ketones, e. g. acetone, methyl-ethyl ketone, etc., the ethers, e. g. ethyl ether, etc., the acetates, e.
- a solvent for use in practicing the invention are: (1) that it be capable of dissolving the fatty oil, and (2) that it be substantially non-freezing, i. c. it will not solidify at the low temperatures employed, a wide choice of solvents is permitted without departing from the scope of the invention.
- drying oils such as linseed oil
- the degree of unsaturation of such oils may be enhanced. For instance, I have found, that the more saturated constituents of the drying oil tend to precipitate at higher temperatures, for instance, between about 20 C. and about 40 C. than the more unsaturated constituents.
- linseed oil is treated at a temperature of about -65 C. over of the oil will be recovered in a highly unsaturated condition.
- the present invention therefore, by enhancing the degree of unsaturation is especially adapted for improving the drying qualities of drying oils.
- the general preferred method of practicing my invention is first to extract the fatty oil from the vegetable or animal fatty 011 containing raw material by any suitable means, either with or without the use of solvents.
- suitable means may include Soxhlet extraction, continuous extraction, dissolving decanted oil, soaking, etc. If no solvent has been employed the raw oil is dissolved in a solvent.
- the fatty oil solution is filtered to remove suspended, insoluble material.
- the solution may then be cooled either to precipitate at once the bulk of the dissolved oil or to bring about fractional crystallization of the oil into portions of varying degrees of saturation.
- the oil is precipitated in a solid, easily fllterable form, separated from the liquid solvent containing the dissolved impurities in any convenient manner, as by decantation or filtration.
- the solid oil is then melted, and freed from any residual small amounts of solvent by known procedures.
- the separated remaining solvent may be purified by distillation and the residual material recovered.
- Example I Crushed fiaxseed is treated with warm acetone until practically all the linseed oil has been extracted Sufficient acetone is used so that the resulting solution will contain about linseed oil.
- the solution is cooled to C. and filtered. About 3% of the linseed oil, 1. e., the more saturated portion thereof will precipitate. The precipitate will also contain waxes, phosphatides, saturated giycerides, mucilaginous materials, etc. This fraction is discarded or used as a by-product.
- the remaining solution is then cooled to 68 C. and filtered. This will remove from solution all but about 4% of the oil.
- the portion of the oil remaining in solution is composed mainly of coloring matter, oxidized material, etc.
- the acetone is recovered by distillation and the residue may be considered a by-product.
- the oil which precipitates out at 68 C. is the main fraction and consists of about 92% of the total oily material in the seed. It is freed if Example II A solution of 10% linseed oil in acetone is cooled to 38 C. and filtered, then the solution chilled to -75 C. and filtered. The following fractions were obtained.
- Example III Tung oil is extracted from the tung apple with acetone. A 10% solution of the oil is cooled to -65 C. At that temperature 96% of the tung oil has precipitated from the solution. After filtering and freeing from the retained solvent, a very much lighter oil containing substantially no impurities is obtained than may be manufactured by pressing or extraction and distillation of the solvent.
- Example IV Castor oil is extracted from the crushed castor bean using a quantity of acetone so that the resulting solution will contain 10% castor oil. The acetone 011 solution is then cooled to --65 C. and the precipitated oil recovered as in the previous examples. 94% of the total castor oil is obtained in this manner which is lighter in color and purer than is obtained by pressing.
- my invention comprises broadly a method of purifying fatty oils by refrigeration, and embraces a means for the 1ractional crystallization of fatty oils which contain saturated and unsaturated constituents whereby the relative proportion of unsaturated constituents is raised while that of the saturated constituents is reduced.
- Method for the treatment of fatty oils containing saturated and unsaturated constituents which comprises cooling a solution of a fatty oil in a non-freezing solvent to a temperature at which the more saturated constituents will precipitate out of solution, separating from the solution the precipitated more saturated constituents together with precipitated impurities, and further cooling the solution to a temperature at which the major portion of the remaining more unsaturated constituents precipitate out of solution.
- Method for th treatment of fatty oils containing saturated and unsaturated portions which comprises cooling a solution of a fatty oil in a non-freezing solvent to temperatures between about -20 C. and down to 40 C., separating from the solution the precipitated more saturated constituents together with precipitated impurities, further cooling the solution to temperatures between 40 C., and down to about -70 C. until the major portion of the remaining'more unsaturated constituents are precipitated out of solution and thereafter separating the precipitated material from the solvent.
- Method for the production of highly unsaturated linseed oil which comprises extracting flaxseed with acetone, filtering the resulting solution, cooling it to about -2 C., separating therefrom precipitated solids, further cooling the solution to about 68 C. and separating the precipitated, highly unsaturated linseed oil from the solvent.
Landscapes
- Chemical & Material Sciences (AREA)
- Analytical Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Fats And Perfumes (AREA)
Description
Patented July 4, 1944 PRODUCTION AND PURIFICATION OF OILS Don Sheldon Bolley, Brooklyn, N. Y., assignor to National Lead Company, New York, N. Y., a corporation of New Jersey No Drawing. Application April 12, 1940,
Serial No. 329,303
6 Claims.
This invention relates to the production and/or purification of fatty oils by a process involving solvent extraction and subsequent precipitation of the oil from the solution by cooling.
One object of the invention is to provide an improved method of freeing the extracted fatty oil from the solvent. Another object of the invention is to provide a method of removing coloring matter, oxidized material, phosphatides, etc., from the fatty oil. Still another object is to provide a method for separating a fatty oil into various fractions of different degrees of unsaturation. Other objects of the invention will become apparent as the description thereof proceeds.
By the term fatty oils as used herein and in the appended claims is meant oils which are derived from fatty oil containing raw material of vegetable or animal origin and which are regarded chemically to be the glycerol esters of high molecular weight aliphatic acids, either saturated or unsaturated and embrace the drying, semi-drying and non-drying oils.
Fatty oils are, at present, produced from fatty oil containing raw materials of either vegetable or animal origin by cooking and allowing the oil to settle out; by pressing, or by solvent extraction. The present invention is concerned with improvements in the methods involving solvent extraction. For the purpose of this description of the present invention a solvent process is considered tobe any process in which th fatty oil in the course of its preparation and/or purification is dissolved in solvents and subsequently separated therefrom. Thus, if the oil is pressed from vegetable or animal material and subsequently dissolved in solvents it is considered a solvent process and the improved methods of the present invention are applicable thereto.
In the prior art, fatty oil is recovered from a solvent solution by distillation of the solvent by the application of heat, vacuum, or both heat and vacuum. Thus, the recovered fatty oil contains any non-volatile impurities which may be contained in the solution whereas the solvent is recovered substantially pure.
I have now found that when a solvent solution is sufliciently cooled, as by the use of artificial refrigeration, the fatty oil will precipitate substantially completely out of the solution in a practically pure state as an easily fllterable solid mass which may be readily separated from any contaminating impurities which remain dissolved in the solvent. I have further found, when cooling fatty oils of the drying and semi-drying types according to the present invention, that at different temperatures various fractions of the oil diflering from each other particularly with respect to degree of unsaturation separate out of the solution. Hence, the present invention provides a means for obtaining a great variety of different oil fraction from the same fatty-oil containing raw material.
. I am aware that the prior art teaches that a portion ofthe saturated fatty oils may be removed from the bulk ofthe fatty oils by chilling either the oil itself or a solution thereof in a suitable solvent and subsequently removing the precipitated solids by filtration. Where solvents are used the bulk of the oil is then recovered, according to these prior art methods, by distilling the solvent, leaving the non-volatile impurities in the fatty oil. In contradistinction to such methods, the present invention contemplates a precipitation of the bulk of the fatty oil in solid condition and the subsequent separation thereof from the solvent which contains the impurities by filtration.
Any solvent commonly used in extracting fatty oil from vegetable or animal oil containing raw materials and which does not solidify at the temperatures employed may be used in practicing the present inventions. Such solvents will include the coal tar derivatives, e. g. mineral spirits, petroleum derivatives, e. g. petroleum spirits, petroleum ether, etc., natural derivatives, e. g. turpentine, the alcohols, e. g. methyl, ethyl, isopropyl, propyl, etc., the ketones, e. g. acetone, methyl-ethyl ketone, etc., the ethers, e. g. ethyl ether, etc., the acetates, e. g., ethyl acetate, etc., the halogenated parafflns, e. g. carbon tetrachloride, chloroform, etc. Since, the only requirements of a solvent for use in practicing the invention are: (1) that it be capable of dissolving the fatty oil, and (2) that it be substantially non-freezing, i. c. it will not solidify at the low temperatures employed, a wide choice of solvents is permitted without departing from the scope of the invention.
I have found that substantially all of the fatty oil in solvent solution will be precipitated when the solution is cooled to temperatures between about 40 C. and -70 C. When drying oils, such as linseed oil, are treated according to the present invention. the degree of unsaturation of such oils may be enhanced. For instance, I have found, that the more saturated constituents of the drying oil tend to precipitate at higher temperatures, for instance, between about 20 C. and about 40 C. than the more unsaturated constituents. When linseed oil is treated at a temperature of about -65 C. over of the oil will be recovered in a highly unsaturated condition. The present invention, therefore, by enhancing the degree of unsaturation is especially adapted for improving the drying qualities of drying oils.
The general preferred method of practicing my invention is first to extract the fatty oil from the vegetable or animal fatty 011 containing raw material by any suitable means, either with or without the use of solvents. Such methods may include Soxhlet extraction, continuous extraction, dissolving decanted oil, soaking, etc. If no solvent has been employed the raw oil is dissolved in a solvent. The fatty oil solution is filtered to remove suspended, insoluble material. The solution may then be cooled either to precipitate at once the bulk of the dissolved oil or to bring about fractional crystallization of the oil into portions of varying degrees of saturation. The oil is precipitated in a solid, easily fllterable form, separated from the liquid solvent containing the dissolved impurities in any convenient manner, as by decantation or filtration. The solid oil is then melted, and freed from any residual small amounts of solvent by known procedures. The separated remaining solvent may be purified by distillation and the residual material recovered.
Example I Crushed fiaxseed is treated with warm acetone until practically all the linseed oil has been extracted Sufficient acetone is used so that the resulting solution will contain about linseed oil. The solution is cooled to C. and filtered. About 3% of the linseed oil, 1. e., the more saturated portion thereof will precipitate. The precipitate will also contain waxes, phosphatides, saturated giycerides, mucilaginous materials, etc. This fraction is discarded or used as a by-product. The remaining solution is then cooled to 68 C. and filtered. This will remove from solution all but about 4% of the oil. The portion of the oil remaining in solution is composed mainly of coloring matter, oxidized material, etc. The acetone is recovered by distillation and the residue may be considered a by-product.
The oil which precipitates out at 68 C. is the main fraction and consists of about 92% of the total oily material in the seed. It is freed if Example II A solution of 10% linseed oil in acetone is cooled to 38 C. and filtered, then the solution chilled to -75 C. and filtered. The following fractions were obtained.
I Precipitating Percent Iodine temp. weight number C'. .20 to -38 11.8 121 38 to 75 85. 4 196 2. 8 191 1 Not precipitated. The iodine number of total oil in the seed was 186. Thus, the middle fraction contains a high percentage of the total oil with an increased iodine number. Therefore, the oil has been fractionated, so that a large proportion of the oil has an iodine number of 10 points higher than the total oil. This is considered an advantage when the oil is to be used as a paint vehicle. Further, the oil has been purified by this treatment. By choosing other precipitating temperatures, fractions of oil having higher or lower iodine numbers may be obtained.
Example III Tung oil is extracted from the tung apple with acetone. A 10% solution of the oil is cooled to -65 C. At that temperature 96% of the tung oil has precipitated from the solution. After filtering and freeing from the retained solvent, a very much lighter oil containing substantially no impurities is obtained than may be manufactured by pressing or extraction and distillation of the solvent.
Example IV Castor oil is extracted from the crushed castor bean using a quantity of acetone so that the resulting solution will contain 10% castor oil. The acetone 011 solution is then cooled to --65 C. and the precipitated oil recovered as in the previous examples. 94% of the total castor oil is obtained in this manner which is lighter in color and purer than is obtained by pressing.
It will be seen from the foregoing description and the illustrative examples given that my invention comprises broadly a method of purifying fatty oils by refrigeration, and embraces a means for the 1ractional crystallization of fatty oils which contain saturated and unsaturated constituents whereby the relative proportion of unsaturated constituents is raised while that of the saturated constituents is reduced.
I claim: 7
1. Method for the treatment of fatty oils containing saturated and unsaturated constituents which comprises cooling a solution of a fatty oil in a non-freezing solvent to a temperature at which the more saturated constituents will precipitate out of solution, separating from the solution the precipitated more saturated constituents together with precipitated impurities, and further cooling the solution to a temperature at which the major portion of the remaining more unsaturated constituents precipitate out of solution.
2. Method for th treatment of fatty oils containing saturated and unsaturated portions which comprises cooling a solution of a fatty oil in a non-freezing solvent to temperatures between about -20 C. and down to 40 C., separating from the solution the precipitated more saturated constituents together with precipitated impurities, further cooling the solution to temperatures between 40 C., and down to about -70 C. until the major portion of the remaining'more unsaturated constituents are precipitated out of solution and thereafter separating the precipitated material from the solvent.
3. Method for the production of highly unsaturated linseed oil which comprises extracting flaxseed with acetone, filtering the resulting solution, cooling it to about -2 C., separating therefrom precipitated solids, further cooling the solution to about 68 C. and separating the precipitated, highly unsaturated linseed oil from the solvent.
4. Method according to claim 1 in which the fatty oil treated is linseed oil.
5. Method according to claim 1 in which the fatty oil treated is tung oil.
6. Method according to claim 1 in which the fatty oil treated is castor oil.
DON SHELDON BOLLEY.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US329303A US2352883A (en) | 1940-04-12 | 1940-04-12 | Production and purification of fatty oils |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US329303A US2352883A (en) | 1940-04-12 | 1940-04-12 | Production and purification of fatty oils |
Publications (1)
Publication Number | Publication Date |
---|---|
US2352883A true US2352883A (en) | 1944-07-04 |
Family
ID=23284781
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US329303A Expired - Lifetime US2352883A (en) | 1940-04-12 | 1940-04-12 | Production and purification of fatty oils |
Country Status (1)
Country | Link |
---|---|
US (1) | US2352883A (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2491350A (en) * | 1944-01-15 | 1949-12-13 | Standard Oil Dev Co | Preparation of purified polyesters |
US2514608A (en) * | 1945-08-30 | 1950-07-11 | Emery Industries Inc | Method of separating glycerides |
US2576841A (en) * | 1946-01-17 | 1951-11-27 | Swift & Co | Solvent fractionation |
US2883405A (en) * | 1954-10-18 | 1959-04-21 | Ranchers Cotton Oil | Method of separating components of cottonseed oil by fractional crystallization of miscella thereof |
US2903363A (en) * | 1954-09-17 | 1959-09-08 | Gerald W Farr | Solvent fractionation of winterized cottonseed oil bottoms |
US3884046A (en) * | 1969-03-26 | 1975-05-20 | Metallgesellschaft Ag | Crystallization of a fatty component from a feed by the steps of emulsification with a surfactant, cooling by vacuum evaporation and subsequent conventional separation |
US4697426A (en) * | 1986-05-29 | 1987-10-06 | Shell Western E&P Inc. | Choke cooling waxy oil |
US4702758A (en) * | 1986-05-29 | 1987-10-27 | Shell Western E&P Inc. | Turbine cooling waxy oil |
US4754613A (en) * | 1985-09-23 | 1988-07-05 | Sanbra-Sociedade Algodoeira Do Nordeste Brasileiro S.A. | Vacuum process for physical deodorization and/or physical refining oils and fats through direct condensation of the vapors |
US9581267B2 (en) | 2011-04-06 | 2017-02-28 | David John Kusko | Hydroelectric control valve for remote locations |
-
1940
- 1940-04-12 US US329303A patent/US2352883A/en not_active Expired - Lifetime
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2491350A (en) * | 1944-01-15 | 1949-12-13 | Standard Oil Dev Co | Preparation of purified polyesters |
US2514608A (en) * | 1945-08-30 | 1950-07-11 | Emery Industries Inc | Method of separating glycerides |
US2576841A (en) * | 1946-01-17 | 1951-11-27 | Swift & Co | Solvent fractionation |
US2903363A (en) * | 1954-09-17 | 1959-09-08 | Gerald W Farr | Solvent fractionation of winterized cottonseed oil bottoms |
US2883405A (en) * | 1954-10-18 | 1959-04-21 | Ranchers Cotton Oil | Method of separating components of cottonseed oil by fractional crystallization of miscella thereof |
US3884046A (en) * | 1969-03-26 | 1975-05-20 | Metallgesellschaft Ag | Crystallization of a fatty component from a feed by the steps of emulsification with a surfactant, cooling by vacuum evaporation and subsequent conventional separation |
US4754613A (en) * | 1985-09-23 | 1988-07-05 | Sanbra-Sociedade Algodoeira Do Nordeste Brasileiro S.A. | Vacuum process for physical deodorization and/or physical refining oils and fats through direct condensation of the vapors |
US4697426A (en) * | 1986-05-29 | 1987-10-06 | Shell Western E&P Inc. | Choke cooling waxy oil |
US4702758A (en) * | 1986-05-29 | 1987-10-27 | Shell Western E&P Inc. | Turbine cooling waxy oil |
US9581267B2 (en) | 2011-04-06 | 2017-02-28 | David John Kusko | Hydroelectric control valve for remote locations |
US9920886B2 (en) | 2011-04-06 | 2018-03-20 | David John Kusko | Hydroelectric control valve for remote locations |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2352883A (en) | Production and purification of fatty oils | |
JPS5936625A (en) | Improvement on manufacture of non-saponifiable compound from natural matter, medicine cosmetics and food composition | |
US2391893A (en) | Production of sugar cane wax | |
JP2000516268A (en) | Triglyceride fractionation | |
US5085808A (en) | Process for efficiently extracting high quality oil from soybeans and other oil bearing seeds | |
US2453543A (en) | Process of treating bituminous coal | |
US2662907A (en) | Process of making refined sugar cane wax | |
US2158670A (en) | Process for the recovery of essential oils | |
US2216904A (en) | Treatment of distillery slop | |
GB2069520A (en) | Process for separating the components of a mixture of fatty compounds | |
US2106200A (en) | Method of extracting perfume materials unstable to heat | |
US3038854A (en) | Solvent dewaxing | |
US2938028A (en) | Purifying and dewaxing citrus oils | |
JPH06200287A (en) | Method for purifying natural crude wax | |
US2347460A (en) | Process for treating fat-soluble vitamin-containing oils | |
US3345389A (en) | Separation of fatty materials | |
US1988031A (en) | Method of recovering carotene | |
US1944958A (en) | Purification of aromatic alcohols | |
US2029261A (en) | Soybean phosphatides | |
US2453544A (en) | Process for preparing and coking bituminous coal | |
US2449107A (en) | Process of making refined sugar-cane wax | |
DE2020973C3 (en) | Process for the production of pure anthracene from the anthracene oil of coal tar | |
US2161569A (en) | Dewaxing hydrocarbon oil | |
US2430012A (en) | Production of sugar cane wax | |
US2028307A (en) | Process for preparing ceresin |