US2164012A - Treatment of nonmineral fatty matter raffinates - Google Patents
Treatment of nonmineral fatty matter raffinates Download PDFInfo
- Publication number
- US2164012A US2164012A US143572A US14357237A US2164012A US 2164012 A US2164012 A US 2164012A US 143572 A US143572 A US 143572A US 14357237 A US14357237 A US 14357237A US 2164012 A US2164012 A US 2164012A
- Authority
- US
- United States
- Prior art keywords
- acid
- ethanolamine
- fatty
- washing
- fatty matter
- 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
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 44
- 238000005406 washing Methods 0.000 description 23
- 238000007670 refining Methods 0.000 description 21
- 239000000344 soap Substances 0.000 description 21
- 239000003795 chemical substances by application Substances 0.000 description 20
- 239000002253 acid Substances 0.000 description 18
- 238000000034 method Methods 0.000 description 11
- 239000007864 aqueous solution Substances 0.000 description 10
- 238000000605 extraction Methods 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000003921 oil Substances 0.000 description 7
- 235000019198 oils Nutrition 0.000 description 7
- 241001125048 Sardina Species 0.000 description 5
- 150000001412 amines Chemical class 0.000 description 5
- 235000021588 free fatty acids Nutrition 0.000 description 5
- 235000019512 sardine Nutrition 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 229910052500 inorganic mineral Inorganic materials 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000011707 mineral Substances 0.000 description 4
- 235000010755 mineral Nutrition 0.000 description 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Substances OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 2
- 239000003925 fat Substances 0.000 description 2
- 235000019197 fats Nutrition 0.000 description 2
- -1 halogen acids Chemical class 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- WIGIZIANZCJQQY-UHFFFAOYSA-N 4-ethyl-3-methyl-N-[2-[4-[[[(4-methylcyclohexyl)amino]-oxomethyl]sulfamoyl]phenyl]ethyl]-5-oxo-2H-pyrrole-1-carboxamide Chemical compound O=C1C(CC)=C(C)CN1C(=O)NCCC1=CC=C(S(=O)(=O)NC(=O)NC2CCC(C)CC2)C=C1 WIGIZIANZCJQQY-UHFFFAOYSA-N 0.000 description 1
- PXRKCOCTEMYUEG-UHFFFAOYSA-N 5-aminoisoindole-1,3-dione Chemical compound NC1=CC=C2C(=O)NC(=O)C2=C1 PXRKCOCTEMYUEG-UHFFFAOYSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 241000592335 Agathis australis Species 0.000 description 1
- 241000252203 Clupea harengus Species 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 235000012716 cod liver oil Nutrition 0.000 description 1
- 239000003026 cod liver oil Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000019688 fish Nutrition 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 235000019514 herring Nutrition 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229940084106 spermaceti Drugs 0.000 description 1
- 239000012177 spermaceti Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
- 239000011686 zinc sulphate Substances 0.000 description 1
- 235000009529 zinc sulphate Nutrition 0.000 description 1
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
- C11B3/00—Refining fats or fatty oils
- C11B3/02—Refining fats or fatty oils by chemical reaction
- C11B3/06—Refining fats or fatty oils by chemical reaction with bases
Definitions
- This invention relates to an improvement in the process for refining fatty matters wherein free fatty acids, mucilaginous material and other undesirable matters are removed by extraction with a nitrogen-containing alkaline refining agent, such as amines, alkylolamines, ammonia, etc., the extractants being anhydrous or in aqueous admixture and used individually or as a mixture with other solvents.
- a nitrogen-containing alkaline refining agent such as amines, alkylolamines, ammonia, etc.
- the fatty matter which may be of animal, vegetable or synthetic origin is extracted in the liquid phase with a suitable amount of an alkaline nitrogencontaining refining agent, such as, for example, ethanolamine or ethylene diamine.
- an alkaline nitrogencontaining refining agent such as, for example, ethanolamine or ethylene diamine.
- suitable agents are described in U. S. Patents Nos. 1,900,132 and 1,885,859.
- the free fatty acids, mucilaginous matter, certain coloring bodies, anti-oxidants, aldehydes and other undesirable materials are substantially removed in the extract phase while the vitamine content of the fatty matter is unaltered.
- the small amount of refining agent remaining in the fatty matter is extracted with successive amounts of water. The first water washes are very effective and remove the major part of the refining agent without difficulty.
- the most important members of this group are of mineral origin and include the halogen acids, sulfuric acid, phosphoric acid and acid- V acting salts such as acid sulfates, ZnClz, ZnSO4, 5 FeCla etc.
- Certain organic acids, as for example citric, lactic and acetic acid have been found to be operative. In general, we use those acid-acting agents in concentrations which, during the washing step, are capable of causing the 10 liberation of the alkaline refining agent from its soap.
- reaction is nearly quantitative, is substantially complete in a very short time (which is dependent upon the degree of mixing), and does not require special conditions as regards temperature, pressure, etc.
- the acid washing is preferably executed while the fatty matter is in the liquid state.
- fatty matter as used heretofore and in the claims is intended to comprehend the general class of organic oils, fats, waxes, and resins of animal, vegetable, or synthetic origin which may be successfully refined through use of the above mentioned refining agents.
- examples of the same are sesame oil, herring oil, cottonseed oil, sardine oil, coconut oil, cocoabuto ter, palm oil, carnauba wax, beef tallow, spermaceti, bush kauri, codliver oil, etc.
- rafiinate designates a fatty matter substantially freed by previous treatment of all undesirable constituents capable of being re- 45 moved by the refining agent in question.
- Percent Percent Acid solution used ethanolamine ggeozliig
- the striking reduction of the ethanolamine content and the constancy of the free fatty acid content are self-evident.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Microbiology (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
UNITED STATES PATENT OFFICE TREATMENT NONMINERAL FATTY MATTER RAFFINATES Walter J. Hund, Oakland, and Ludwig Rosenstein, San Francisco, Calif., assignors to Shell Development Company, San Francisco, Calif., a corporation of Delaware No Drawing. Application May 19, 1937,
- Serial No. 143,572
8 Claims.
This invention relates to an improvement in the process for refining fatty matters wherein free fatty acids, mucilaginous material and other undesirable matters are removed by extraction with a nitrogen-containing alkaline refining agent, such as amines, alkylolamines, ammonia, etc., the extractants being anhydrous or in aqueous admixture and used individually or as a mixture with other solvents.
More specifically, it consists in removing the last traces of the refining agent from the treated fatty matter by washing with a weakly acid aqueous solution of an acid-acting agent.
According to the present practice, the fatty matter, which may be of animal, vegetable or synthetic origin is extracted in the liquid phase with a suitable amount of an alkaline nitrogencontaining refining agent, such as, for example, ethanolamine or ethylene diamine. Other suitable agents are described in U. S. Patents Nos. 1,900,132 and 1,885,859. The free fatty acids, mucilaginous matter, certain coloring bodies, anti-oxidants, aldehydes and other undesirable materials are substantially removed in the extract phase while the vitamine content of the fatty matter is unaltered. The small amount of refining agent remaining in the fatty matter is extracted with successive amounts of water. The first water washes are very effective and remove the major part of the refining agent without difficulty. The remaining trace of refining agent which exists in the raffinate predominantly in the form of a soap is very difficult to remove even with repeated water washing. A conventional method used to remove the last traces of refining agent is to blow the heated raffinate with an inert gas under reduced pressure. This method has the objections of requiring costly equipment and considerable operating expense.
The presence of even traces of such soaps may be objectionable, if they impart a disagreeable taste, lower the resistance to rancidification, promote discoloration, orpromote sludge formation on aging.
We have found that if, in the removal of the last traces of refining agent by water washing, the last water wash is replaced by a wash with an aqueous weakly acid solution, as, for example, a dilute solution of hydrochloric acid, that the refining agent is liberated from its soap and completely removed while the free fatty acid content of the rafiinate is unaltered.
Any material which is at least moderately soluble in water, substantially insoluble in the fatty matter in question and shows an acid reaction when in aqueous solution, is a suitable acid-acting agent. The most important members of this group are of mineral origin and include the halogen acids, sulfuric acid, phosphoric acid and acid- V acting salts such as acid sulfates, ZnClz, ZnSO4, 5 FeCla etc. Certain organic acids, as for example citric, lactic and acetic acid have been found to be operative. In general, we use those acid-acting agents in concentrations which, during the washing step, are capable of causing the 10 liberation of the alkaline refining agent from its soap.
The reaction is nearly quantitative, is substantially complete in a very short time (which is dependent upon the degree of mixing), and does not require special conditions as regards temperature, pressure, etc.
As is the case with ordinary water washing, the acid washing is preferably executed while the fatty matter is in the liquid state. This requires '20 slightly elevated temperatures when dealing with fats, waxes, resins, etc., which are solid at ordinary temperatures. Elevated temperatures reduce the viscosity of the fatty matters and thereby the rate of phase separation, which is, in 2 many cases, advantageous.
Since the reaction is nearly quantitative, approximately the stoichiometric amount of acid is preferably used. A moderate excess of acid is, however, not detrimental. It is obvious that only '30 small quantities of acid are required and that no acid need be wasted.
The term fatty matter as used heretofore and in the claims is intended to comprehend the general class of organic oils, fats, waxes, and resins of animal, vegetable, or synthetic origin which may be successfully refined through use of the above mentioned refining agents. Examples of the same are sesame oil, herring oil, cottonseed oil, sardine oil, coconut oil, cocoabuto ter, palm oil, carnauba wax, beef tallow, spermaceti, bush kauri, codliver oil, etc.
The term rafiinate designates a fatty matter substantially freed by previous treatment of all undesirable constituents capable of being re- 45 moved by the refining agent in question.
As illustrative of the effectiveness of our invention, we offer the following experimental results, which, it is to be understood, are not to be regarded as limiting the scope of the invention 50 as regards material treated, acids used, time of contact, proportions of matter or the like.
A corn oil raffinate, refined by the use of ethanolamine and washed twice with water, contained 0.032% ethanolamine and 0.103% free 5 fatty acid (as oleic). Only by repeated washing and filtering in the laboratory under uneconomic conditions could these values be finally reduced to 0.007% ethanolamine and 0.053% free acid (as oleic). Portions of the well washed raffinate were thereupon washed for two minutes with 4% by volume of 0.03 normal acid solutions and filtered. This corresponds to 10% acid in excess over the stoichiometric requirement. The results are shown in the following table:
Percent Percent Acid solution used ethanolamine ggeozliig The striking reduction of the ethanolamine content and the constancy of the free fatty acid content are self-evident.
Our improved process offers distinct advantages since through the execution of our invention we are able, with little expense, to remove the before-mentioned undesirable soaps from fatty matters and thereby improve their quality as regards taste, color stability, etc., without affecting the content of free fatty acid.
We claim as our invention:
1. In a process for the refining of fatty matters with a nitrogen-containing alkaline extractant, the steps of first water-washing the raflinate obtained by the main extraction until substantially no free extractant is included therein and subsequently washing the ralfinate with a minor volume of a dilute aqueous solution of an acidacting agent at least stoichiometrically equivalent to the soaps present in the treated raflinate whereby the extractant combined as soaps is liberated and simultaneously substantially removed from the fatty matter.
2. In a process for the refining of fatty matters by extracting with an amine, the steps of first Water-washing the rafiinate obtained by the main extraction until substantially no free amine is included therein and subsequently washing the rafiinate with a minor portion of a dilute aqueous solution of an acid-acting agent at least stoichiometrically equivalent to the amine soaps present in the treated rafiinate whereby the amine combined as soap is liberated and simultaneously substantially removed from the fatty matter.
3. In a process for the refining of fatty matters by extracting with an alkanolamine, the steps of first water-washing the rafiinate obtained by the main extraction until substantially no free alkanolamine is included therein and subsequently Washing the raffinate with a minor portion of a dilute aqueous solution of an acid-acting agent at least stoichiometrically equivalent to the alkanolamine soap present in the treated rafiinate whereby the alkanolamine combined as soap is liberated and simultaneously substantially A; moved from the fatty matter.
4. In a process for the refining of fatty matters by extracting with an ethanolamine, the steps of first water-washing the rafflnate obtained by the main extraction until substantially no free ethanolamine is included therein and subsequently washing the raflinate with a minor portion of a dilute aqueous solution of an acid-acting agent at least stoichiometrically equivalent to the ethanolamine soaps present in the treated raffinate whereby the ethanolamine combined as soaps is liberated and simultaneously substantially removed from the fatty matter.
5. In a process for the refining of fatty matter with a nitrogen-containing alkaline extractant, the steps of first water-washing the raflmate obtained by the main extraction until substantially no free extractant is included therein and subsequently washing the rafiinate with a minor volume of a dilute aqueous solution of a mineral acid at least stoichiometrically equivalent to the soaps present in the treated rafiinate whereby the extractant combined as soaps is liberated and simultaneously substantially removed from the fatty matter.
6. In a process for the refining of fatty matter of fish origin by extracting with an ethanolamine, the steps of first water-washing the rafiinate obtained by the main extraction until substantially no free ethanolamine is included therein and subsequently washing the rafiinate with a minor portion of a dilute aqueous solution of a mineral acid at least stoichiometrically equivalent to the ethanolamine soaps present in the treated raffinate whereby the ethanolamine combined as soaps is liberated and simultaneously substantially' removed from the fatty matter.
7. In a process for the refining of sardine oil by extracting with an ethanolamine, the steps of first water-washing the rafiinate obtained by the main extraction until substantially no free ethanolamine is included therein and subsequently washing the rafilnate with a minor portion of a dilute aqueous solution of a mineral acid at least stoichiometrically equivalent to the ethanolamine soaps present in the treated rafiinate whereby the ethanolamine combined as soaps is liberated and simultaneously substantially removed from the sardine oil.
8. In a process for the refining of sardine oil by extracting with an ethanolamine, the steps of first water-washing the raffinate obtained by the main extraction until substantially no free ethanolamine is included therein and subsequently Washing the rafiinate with a minor portion of a dilute aqueous solution of hydrochloric acid at least stoichiometrically equivalent to the ethanolamine soaps present in the treated rafiinate whereby the ethanolamine combined as soaps is liberated and simultaneously substantially removed from the sardine oil.
WALTER J. HUND. LUDWIG ROSENSTEIN.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US143572A US2164012A (en) | 1937-05-19 | 1937-05-19 | Treatment of nonmineral fatty matter raffinates |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US143572A US2164012A (en) | 1937-05-19 | 1937-05-19 | Treatment of nonmineral fatty matter raffinates |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2164012A true US2164012A (en) | 1939-06-27 |
Family
ID=22504644
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US143572A Expired - Lifetime US2164012A (en) | 1937-05-19 | 1937-05-19 | Treatment of nonmineral fatty matter raffinates |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2164012A (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2463015A (en) * | 1948-03-17 | 1949-03-01 | Frederick C Bersworth | Method of treating animal and vegetable oils |
| US2510379A (en) * | 1948-08-31 | 1950-06-06 | Pittsburgh Plate Glass Co | Preparation of break-free glyceride oils |
| US2686794A (en) * | 1950-09-14 | 1954-08-17 | Clayton Benjamin | Ammonia treatment of glyceride oils, and products resulting therefrom |
| US2787625A (en) * | 1953-08-12 | 1957-04-02 | Joseph M Dechary | Cottonseed oil color reversion prevention |
| US2881195A (en) * | 1955-04-15 | 1959-04-07 | Staley Mfg Co A E | Refining vegetable oils |
| US3142700A (en) * | 1961-08-04 | 1964-07-28 | Sturzenegger | |
| US6579996B2 (en) | 1999-04-21 | 2003-06-17 | Siegfried Peter | Process for removing free fatty acids from fats and oils of biological origin or their steam distillates |
| WO2020089605A1 (en) | 2018-10-29 | 2020-05-07 | Green Lizard Technologies Ltd. | Chloropropanol removal process |
| WO2020089603A1 (en) | 2018-10-29 | 2020-05-07 | Green Lizard Technologies Ltd. | Metal removal process |
| WO2020089601A1 (en) | 2018-10-29 | 2020-05-07 | Green Lizard Technologies Ltd. | Phosphorus removal process |
-
1937
- 1937-05-19 US US143572A patent/US2164012A/en not_active Expired - Lifetime
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2463015A (en) * | 1948-03-17 | 1949-03-01 | Frederick C Bersworth | Method of treating animal and vegetable oils |
| US2510379A (en) * | 1948-08-31 | 1950-06-06 | Pittsburgh Plate Glass Co | Preparation of break-free glyceride oils |
| US2686794A (en) * | 1950-09-14 | 1954-08-17 | Clayton Benjamin | Ammonia treatment of glyceride oils, and products resulting therefrom |
| US2787625A (en) * | 1953-08-12 | 1957-04-02 | Joseph M Dechary | Cottonseed oil color reversion prevention |
| US2881195A (en) * | 1955-04-15 | 1959-04-07 | Staley Mfg Co A E | Refining vegetable oils |
| US3142700A (en) * | 1961-08-04 | 1964-07-28 | Sturzenegger | |
| US6579996B2 (en) | 1999-04-21 | 2003-06-17 | Siegfried Peter | Process for removing free fatty acids from fats and oils of biological origin or their steam distillates |
| WO2020089605A1 (en) | 2018-10-29 | 2020-05-07 | Green Lizard Technologies Ltd. | Chloropropanol removal process |
| WO2020089603A1 (en) | 2018-10-29 | 2020-05-07 | Green Lizard Technologies Ltd. | Metal removal process |
| WO2020089601A1 (en) | 2018-10-29 | 2020-05-07 | Green Lizard Technologies Ltd. | Phosphorus removal process |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP3711023B2 (en) | Methods for removing free fatty acids from biologically derived fats and oils or their vapor distillates | |
| US2596344A (en) | Fractionation process | |
| US2164012A (en) | Treatment of nonmineral fatty matter raffinates | |
| US2413009A (en) | Processes of refining, purifying, and hydrogenating fats, fatty acids, and waxes | |
| US2113960A (en) | Method of separating saturated and unsaturated higher aliphatic organic compounds from mixtures thereof | |
| US2510379A (en) | Preparation of break-free glyceride oils | |
| US2602807A (en) | Recovery of catalyst from hydrogenated oil | |
| US2525702A (en) | Purification of oil | |
| US2318747A (en) | Provitamin a extraction process | |
| Diosady et al. | Chemical degumming of canola oils | |
| DE2743443A1 (en) | PROCEDURE FOR THE REMOVAL OF ORGANIC LEWIS ACIDS FROM A FLUID NOT MIXABLE WITH WATER | |
| US2416146A (en) | Refining fats and oils | |
| US2255875A (en) | Process of refining vitaminiferous oils | |
| US2090738A (en) | Process of purifying oil and vitamin fractions thereof | |
| US2273045A (en) | Process for recovering sterols | |
| US1926648A (en) | Purification of sulphur-oil | |
| US2268786A (en) | Process for refining fatty compounds | |
| US2374924A (en) | Refining of animal and vegetable oils | |
| US2204109A (en) | Vegetable oil refining | |
| US2228038A (en) | Process for refining ester type oils, fats, and waxes | |
| US1889652A (en) | Process for the distillation of mixed substances of which soap is a constituent | |
| US2275186A (en) | Process for refining tall oil | |
| US2075871A (en) | Process of treating petroleum products | |
| US2265020A (en) | Process for refining fatty acids | |
| US2465969A (en) | Purification of a fatty oil |