US2444720A - Manufacture of lithium base greases - Google Patents
Manufacture of lithium base greases Download PDFInfo
- Publication number
- US2444720A US2444720A US622933A US62293345A US2444720A US 2444720 A US2444720 A US 2444720A US 622933 A US622933 A US 622933A US 62293345 A US62293345 A US 62293345A US 2444720 A US2444720 A US 2444720A
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- US
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- Prior art keywords
- lithium
- soap
- temperature
- acid
- lithium hydroxide
- Prior art date
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- Expired - Lifetime
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/16—Paraffin waxes; Petrolatum, e.g. slack wax
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/16—Naphthenic acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/18—Tall oil acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/20—Rosin acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/02—Groups 1 or 11
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/10—Semi-solids; greasy
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2060/00—Chemical after-treatment of the constituents of the lubricating composition
- C10N2060/04—Oxidation, e.g. ozonisation
Definitions
- This invention relates to the manufacture of lubricants containing lithium soaps such as liquid lubricants and greases.
- lithium soap greases i. e., greases consisting of lithium soaps such ,as lithium stearate and a mineral oil
- the temperature employed reaches 200 C., a temperature which introduces dimculties in the case of greases which have to function under low temperature conditions in which the mineral oil base is necessarily of low viscosity and relatively high volatility.
- a high temperature process is necessary when the lithium is added to the oil in the form of a lithium soap or when it is mixed in as an aqueous solution of lithium hydroxide which is combined with a fatty acid in the presence of the oil.
- the present invention provides in a process for the manufacture of lubricants containing lithium soaps the improvement comprising intimately contacting a quantity of a free soap-forming acid containing at least sixteen carbon atoms in the molecule in solution in a lubricating oil with an approximately equivalent quantity of a saponifying agent of the group consisting of lithium oxide, anhydrous lithium hydroxide, lithium hydroxide and its hydrates at a temperature preferably between 35 and 45 C. for a time sufficient to react at least 90% by weight of one of said lithium compounds and said acid to form a soap.
- the water of reaction is subsequently removed from the lubricant by heating, preferably to a temperature not exceeding 110 C. It is undesirable, however, to employ a higher temperature than is necessary as this increases losses due to vaporisation of the oil base and a temperature of 105 to 110 C. at atmospheric pressure has been found quite suitable. Naturally, lower temperatures can be employed if the operation is carried out under reduced pressure.
- the removal of the-water of reaction is effected by heating in thin layers for example on a rotary film drier such as a Kestner double drum film drier.
- the lithium hydroxide or oxide should preferably be fine enough to pass a 100 mesh B. S. S. sieve.
- stearic acid as the soap forming acid but other fatty acids containing at least sixteen carbon atoms in the molecule may be employed for example palmitic acid, arachic acid, hydroxy-stearic acids, oleic acid, ricinoleic acid, mixed fatty acids such as may be obtained from various fats such as tallow, lard and various seed oils, wool fat acids, naphthenic acids such as may be derived from petroleum oils, rosin acids, tall oil acids, acids produced by the oxidation of paraffin wax or produced by the controlled oxidation of hydrocarbons and acids from montan wax and beeswax.
- other fatty acids containing at least sixteen carbon atoms in the molecule may be employed for example palmitic acid, arachic acid, hydroxy-stearic acids, oleic acid, ricinoleic acid, mixed fatty acids such as may be obtained from various fats such as tallow, lard and various seed oils, wool fat acids, naphthenic acids such as
- Mineral oils suitable for making the greases may be paraffinic or naphthenic preferably having a low content of aromatics and an aniline point of at least 80 C. with a difference in aniline point before and alter sulphation not exceeding 15 C. Oils which do not have such aniline points yield greases which are soft and bleed badly or do not yield greases at all. Therefore best results are obtained with solvent-extracted oils, 1. e., oils from which the bulk of aromatics has been removed for example by extraction with liquid S02. phenol, furfural, nitrobenzene, aniline, sulpholane, etc. In general, the oils fall within the range of lubricating oils.
- the oil If the grease is to be used for low temperature operation, it is of course essential that the oil have both a very low viscosity and a very low pourpoint. In this event a relatively high viscosity index is also desirable, but not essential.
- suitable oils are Edeleanised transformer oils after acid and earth treatments, finished transformer oils, a light distillate prepared from a naphthenic crude which has been Edeleanised and finally treated with activated earth and lime, having a viscosity of Redwood I at 70 F. of about seconds, a technical white oil of viscosity about seconds Redwoodl at F., and a light parafiinous distillate of the mineral Colza type having a viscosity of 45 seconds Redwood I at 70 F.
- the finished lubricants should contain between 7 and 40% preferably 10% to 20% by weight of lithium soap for greases and between 0.25 and 7% by weight of lithium soap for liquid lubricants.
- the lithium oxide and the soap-forming acid are brought together in approximately stoichiometric quantities, and it is preferable to have a slight exceess of the acid over the lithium oxide.
- the reaction may be carried out continuously or in batch.
- a lubricant containing a lithium soap consisting essentially of intimately contacting a quantity of a free soap-forming acid containing at least sixteen carbon atoms in the molecule in solution in a lubricating oil with an approximately equivalent quantity of a saponifying agent of the group consisting of lithium oxide, anhydrous lithium hydroxide, lithium hydroxide and its hydrates at a temperature of between about 35 and 45 C. for a time suflicient to react at least 90% by weight of one of said lithium compounds and said acid to form a soap.
- a lubricant containing a lithium soap consisting essentially of intimately contacting a quantity of a free soap-forming acid containing at least sixteen carbon atoms in the molecule in solution in a lubricating oil with an approximately equivalent amount of a saponiiying agent of the group consisting of lithium oxide, anhydrous lithium hydroxide, lithium hydroxide and its hydrates at a. temperature between about 35 and 45 C. for a time suflicient to react at least 90% by.
- a lithium soap grease consisting essentially of intimately contacting a quantity of a free soap-forming acid containing at least sixteen carbon atoms in the molecule in solution in a lubricating oil with an approximately equivalent quantity of a saponifying agent of the group consisting of lithium oxide, anhydrous lithium hydroxide, lithium hydroxide and its hydrates at a temperature between about 35 and 45 C., for a time sufilcient to cause one of said lithium compounds and acid to react and to form a soap, thereby causing the grease to set, said quantities being such that the reacted mixture contains between about 7 and 40% of said soap.
- a lubricant containing a lithium soap consisting essentially of initially contacting a quantity of free soap-forming acid containing at least 16 carbon atoms in the molecule in solution in a lubricating oil with an approximately equivalent quantity of a saponifying agent selected from the class consisting of lithium oxide, anhydrous lithium hydroxide, lithium hydroxide, and its hydrates at a temperature of about 40 C. for a time suflicient to react at least 90% by Weight of one of said lithium compounds and said acid to form a soap, and thereafter removing water from the resulting mixture by heating the product to a temperature between about 105-410 C. in thin layers.
- a saponifying agent selected from the class consisting of lithium oxide, anhydrous lithium hydroxide, lithium hydroxide, and its hydrates
- a lubricant containing a lithium soap consisting essentially of intimately contacting a quantity of stearic acid in solution in a lubricating oil with an approximately equivalent amount of anhydrous lithium hydroxide at a temperature of about 40 C. for a time sufiicient to react at least by weight of said anhydrous lithium hydroxide and said stearic acid to form the soap.
- a lubricant containing a lithium soap consisting essentially of intimately contacting a suspension of about .25 parts by weight of anhydrous lithium hydroxide in about 5 parts by weight of a lubricating oil with about 14 parts of weight of stearic acid in about 79.95 parts by weight of foresaid lubricating oil at a temperature of about 40 C. to form the soap and thereafter heating the resulting product to a temperature between about to C. in thin layers.
- a lubricant containing a lithium soap consisting essentially of intimately contacting a quantity of free soap-forming acid containing at least 16 carbon atoms in the molecule in solution in a lubricating oil with an approximately equivalent quantity of a saponifying agent of the group consisting of lithium oxide, anhydrous lithium hydroxide, lithium hydroxide and its hydrate at a temperature of between about 35 and 45 C. for a time sufiicient to react at least 90% by weight of bile of said lithium compounds and said acid to form a soap and dehydrating said grease in thin layers.
- a lubricant containing a lithium soap consisting essentially of intimately contacting a quafntity of stearic acid in solution in a lubricating oil with an approximately equivalent amount of anhydrous lithium hydroxide at a temperature of about 40 C. for a time suflicient to react at least 90% by weight of said anhydrous lithium hydroxide and said stearic acid to form the soap and dehydrating said grease in thin layers.
- a lubricant containing a lithium soap comprising intimately contacting a suspension of about 1.25 parts by weight of anhydrous lithium hydroxide in about 5 parts by weight of a lubri- 6 eating oil with about 14 parts by weight of stearic acid in about 79.95 parts by weight of foresaid lubricating oil at a temperature of about C. to form the soap and dehydrating said grease in thin layers.
Description
Patented July 6, 1948 MANUFACTURE OF LITHIUM BASE GREASES James Alfred Bell, Fetcham, Leatherhead, England, assignor to Shell Development Company, San Francisco, Calii., a corporation of Delaware No Drawing. Application October 17, 1945, Se-
rial No. 622,933. In Great Britain October 17, 1944 13 Claims.
This invention relates to the manufacture of lubricants containing lithium soaps such as liquid lubricants and greases.
In the usual processes for the manufacture of lithium soap greases, i. e., greases consisting of lithium soaps such ,as lithium stearate and a mineral oil, the temperature employed reaches 200 C., a temperature which introduces dimculties in the case of greases which have to function under low temperature conditions in which the mineral oil base is necessarily of low viscosity and relatively high volatility. However, a high temperature process is necessary when the lithium is added to the oil in the form of a lithium soap or when it is mixed in as an aqueous solution of lithium hydroxide which is combined with a fatty acid in the presence of the oil.
It is an object of the present invention to avoid the difficulties arising from the use of temperatures of 200 C. or thereabouts and with this object in view the present invention provides in a process for the manufacture of lubricants containing lithium soaps the improvement comprising intimately contacting a quantity of a free soap-forming acid containing at least sixteen carbon atoms in the molecule in solution in a lubricating oil with an approximately equivalent quantity of a saponifying agent of the group consisting of lithium oxide, anhydrous lithium hydroxide, lithium hydroxide and its hydrates at a temperature preferably between 35 and 45 C. for a time sufficient to react at least 90% by weight of one of said lithium compounds and said acid to form a soap.
The water of reaction is subsequently removed from the lubricant by heating, preferably to a temperature not exceeding 110 C. It is undesirable, however, to employ a higher temperature than is necessary as this increases losses due to vaporisation of the oil base and a temperature of 105 to 110 C. at atmospheric pressure has been found quite suitable. Naturally, lower temperatures can be employed if the operation is carried out under reduced pressure.
Preferably the removal of the-water of reaction is effected by heating in thin layers for example on a rotary film drier such as a Kestner double drum film drier.
The lithium hydroxide or oxide should preferably be fine enough to pass a 100 mesh B. S. S. sieve.
It is preferred to use stearic acid as the soap forming acid but other fatty acids containing at least sixteen carbon atoms in the molecule may be employed for example palmitic acid, arachic acid, hydroxy-stearic acids, oleic acid, ricinoleic acid, mixed fatty acids such as may be obtained from various fats such as tallow, lard and various seed oils, wool fat acids, naphthenic acids such as may be derived from petroleum oils, rosin acids, tall oil acids, acids produced by the oxidation of paraffin wax or produced by the controlled oxidation of hydrocarbons and acids from montan wax and beeswax.
Mineral oils suitable for making the greases may be paraffinic or naphthenic preferably having a low content of aromatics and an aniline point of at least 80 C. with a difference in aniline point before and alter sulphation not exceeding 15 C. Oils which do not have such aniline points yield greases which are soft and bleed badly or do not yield greases at all. Therefore best results are obtained with solvent-extracted oils, 1. e., oils from which the bulk of aromatics has been removed for example by extraction with liquid S02. phenol, furfural, nitrobenzene, aniline, sulpholane, etc. In general, the oils fall within the range of lubricating oils.
If the grease is to be used for low temperature operation, it is of course essential that the oil have both a very low viscosity and a very low pourpoint. In this event a relatively high viscosity index is also desirable, but not essential.
Examples of suitable oils are Edeleanised transformer oils after acid and earth treatments, finished transformer oils, a light distillate prepared from a naphthenic crude which has been Edeleanised and finally treated with activated earth and lime, having a viscosity of Redwood I at 70 F. of about seconds, a technical white oil of viscosity about seconds Redwoodl at F., and a light parafiinous distillate of the mineral Colza type having a viscosity of 45 seconds Redwood I at 70 F. I
The finished lubricants should contain between 7 and 40% preferably 10% to 20% by weight of lithium soap for greases and between 0.25 and 7% by weight of lithium soap for liquid lubricants.
The lithium oxide and the soap-forming acid are brought together in approximately stoichiometric quantities, and it is preferable to have a slight exceess of the acid over the lithium oxide. The reaction may be carried out continuously or in batch.
The following example, in which the parts are by weight, illustrates how the process of the invention may be carried into efiect:
' A suspension of 1.25 parts of anhydrous lithium hydroxide passing a 100 mesh B. S. S. sieve in 5.0 parts of a mineral oil prepared by solvent extracmixing the components.
tion from a gas oil fraction having the following characteristics S. G. at 60/60 F 0.890 Viscosity Redwood I at 70 F "secs-.. 61 Flash point Clsd. P. M F 275 Pour Point F -'l0 Refractive index at 50 C 1.4845
A. S. T. M. distillation:
C. I. B. P. 282.5 30% distils to 300 50% distils to 306 70% distlls to 313 90% distiis to 324 Maximum temperature 340 said mineral oil having the following characteristics:
80% recovered at 317.5 90% recovered at 324 Maximum temperature 340 Recovery Per cent Distillate 98.0 Residue 1.5 Loss 0.5
was added with stirring to a solution of 14.0 parts of stearic acid in 79.75 parts of the aforesaid mineral oil at a temperature of 40 C. If higher temperatures are employed at this stage a softer and less smooth product is obtained. Reaction between the lithium hydroxide and stearic acid proceeds rapidly under such conditions and appreciable thickening occurs within 1-2 minutes of The water of reaction is subsequently evaporated by heating the product to a temperature of 105-1 C. in thin layers on a rotary film drier.
What I claim is:
1. In a process of manufacturing a lubricant containing a lithium soap, the improvement consisting essentially of intimately contacting a quantity of a free soap-forming acid containing at least sixteen carbon atoms in the molecule in solution in a lubricating oil with an approximately equivalent quantity of a saponifying agent of the group consisting of lithium oxide, anhydrous lithium hydroxide, lithium hydroxide and its hydrates at a temperature of between about 35 and 45 C. for a time suflicient to react at least 90% by weight of one of said lithium compounds and said acid to form a soap.
2. The process of claim 1 wherein the soapforming acid is stearic acid.
3. The process of claim 1 wherein the lubricating oil has an aniline point of at least 80 C.
4 and a difference in aniline point before and after sulphation of not more than 15 C.
4. The process of claim 1 wherein the saponiiying agent is lithium oxide.
5. The process of claim 1 wherein said saponitying agent is anhydrous lithium hydroxide.
6. In the process of manufacturing a lubricant containing a lithium soap, the improvement consisting essentially of intimately contacting a quantity of a free soap-forming acid containing at least sixteen carbon atoms in the molecule in solution in a lubricating oil with an approximately equivalent amount of a saponiiying agent of the group consisting of lithium oxide, anhydrous lithium hydroxide, lithium hydroxide and its hydrates at a. temperature between about 35 and 45 C. for a time suflicient to react at least 90% by.
weight of one of said lithium compounds and said soap-forming acid to form a soap, and thereafter removing water from the resulting mixture by heating it to a temperature not above about 110 C.
7. In the process of manufacturing a lithium soap grease, the improvement consisting essentially of intimately contacting a quantity of a free soap-forming acid containing at least sixteen carbon atoms in the molecule in solution in a lubricating oil with an approximately equivalent quantity of a saponifying agent of the group consisting of lithium oxide, anhydrous lithium hydroxide, lithium hydroxide and its hydrates at a temperature between about 35 and 45 C., for a time sufilcient to cause one of said lithium compounds and acid to react and to form a soap, thereby causing the grease to set, said quantities being such that the reacted mixture contains between about 7 and 40% of said soap.
8. In a process of manufacturing a lubricant containing a lithium soap, the improvement consisting essentially of initially contacting a quantity of free soap-forming acid containing at least 16 carbon atoms in the molecule in solution in a lubricating oil with an approximately equivalent quantity of a saponifying agent selected from the class consisting of lithium oxide, anhydrous lithium hydroxide, lithium hydroxide, and its hydrates at a temperature of about 40 C. for a time suflicient to react at least 90% by Weight of one of said lithium compounds and said acid to form a soap, and thereafter removing water from the resulting mixture by heating the product to a temperature between about 105-410 C. in thin layers.
9. In a process of manufacturing a lubricant containing a lithium soap, the improvement consisting essentially of intimately contacting a quantity of stearic acid in solution in a lubricating oil with an approximately equivalent amount of anhydrous lithium hydroxide at a temperature of about 40 C. for a time sufiicient to react at least by weight of said anhydrous lithium hydroxide and said stearic acid to form the soap.
10. In a process of manufacturing a lubricant containing a lithium soap, the improvement consisting essentially of intimately contacting a suspension of about .25 parts by weight of anhydrous lithium hydroxide in about 5 parts by weight of a lubricating oil with about 14 parts of weight of stearic acid in about 79.95 parts by weight of foresaid lubricating oil at a temperature of about 40 C. to form the soap and thereafter heating the resulting product to a temperature between about to C. in thin layers.
11. In a process of manufacturing a lubricant containing a lithium soap, the improvement consisting essentially of intimately contacting a quantity of free soap-forming acid containing at least 16 carbon atoms in the molecule in solution in a lubricating oil with an approximately equivalent quantity of a saponifying agent of the group consisting of lithium oxide, anhydrous lithium hydroxide, lithium hydroxide and its hydrate at a temperature of between about 35 and 45 C. for a time sufiicient to react at least 90% by weight of bile of said lithium compounds and said acid to form a soap and dehydrating said grease in thin layers.
12. In a process of manufacturing a lubricant containing a lithium soap, the improvement consisting essentially of intimately contacting a quafntity of stearic acid in solution in a lubricating oil with an approximately equivalent amount of anhydrous lithium hydroxide at a temperature of about 40 C. for a time suflicient to react at least 90% by weight of said anhydrous lithium hydroxide and said stearic acid to form the soap and dehydrating said grease in thin layers.
13. In a process of manufacturing a lubricant containing a lithium soap, the improvement comprising intimately contacting a suspension of about 1.25 parts by weight of anhydrous lithium hydroxide in about 5 parts by weight of a lubri- 6 eating oil with about 14 parts by weight of stearic acid in about 79.95 parts by weight of foresaid lubricating oil at a temperature of about C. to form the soap and dehydrating said grease in thin layers.
JAMES ALFRED BELL.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS OTHER REFERENCES Klemgard, Lubricating Greases, published 1937 by Reinhold Publishing Corporation, of New York, pages 419, 420, 4.79, and 480.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB20082/44A GB583303A (en) | 1944-10-17 | 1944-10-17 | Improvements in or relating to the manufacture of lithium base greases |
Publications (1)
Publication Number | Publication Date |
---|---|
US2444720A true US2444720A (en) | 1948-07-06 |
Family
ID=10140067
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US622933A Expired - Lifetime US2444720A (en) | 1944-10-17 | 1945-10-17 | Manufacture of lithium base greases |
Country Status (3)
Country | Link |
---|---|
US (1) | US2444720A (en) |
FR (1) | FR926608A (en) |
GB (1) | GB583303A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2576031A (en) * | 1948-10-30 | 1951-11-20 | Standard Oil Dev Co | Lubricating grease containing soaps of tall oil |
US2697693A (en) * | 1951-11-05 | 1954-12-21 | Standard Oil Co | Manufacture of lithium hydroxy carboxylic acid soap greases |
US2801220A (en) * | 1954-07-06 | 1957-07-30 | Baker Castor Oil Co | Production of lubricating greases from monohydric alcohol esters of hydroxy fatty acids |
US2860151A (en) * | 1954-01-20 | 1958-11-11 | Lamson Edward Robert | Method for the manufacture of soap |
US2888402A (en) * | 1954-04-07 | 1959-05-26 | Exxon Research Engineering Co | Process for preparing lubricating greases |
US2898298A (en) * | 1954-03-16 | 1959-08-04 | Sinclair Refining Co | Process for lithium base grease |
US2929781A (en) * | 1956-04-18 | 1960-03-22 | Exxon Research Engineering Co | Process for making a lithium-calcium base grease |
US2959548A (en) * | 1955-11-25 | 1960-11-08 | Exxon Research Engineering Co | Process for forming a lithium-calcium grease composition |
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US1753659A (en) * | 1926-05-13 | 1930-04-08 | Vaman R Kokatnur | Anhydrous soap gels and method of making same |
US2350906A (en) * | 1938-05-20 | 1944-06-06 | Frank S Busser | Lubricant grease |
US2351384A (en) * | 1942-11-18 | 1944-06-13 | Shell Dev | Lithium soap grease |
US2363013A (en) * | 1941-12-30 | 1944-11-21 | Standard Oil Dev Co | Stable lubricating composition |
US2382531A (en) * | 1942-08-17 | 1945-08-14 | Auer Laszlo | Soap manufacture |
US2383904A (en) * | 1942-08-12 | 1945-08-28 | Standard Oil Dev Co | Lubricant manufacture |
US2383906A (en) * | 1942-10-28 | 1945-08-28 | Standard Oil Dev Co | Improved manufacture |
US2390450A (en) * | 1942-01-22 | 1945-12-04 | Cities Service Oil Co | Lithium base greases |
-
1944
- 1944-10-17 GB GB20082/44A patent/GB583303A/en not_active Expired
-
1945
- 1945-10-17 US US622933A patent/US2444720A/en not_active Expired - Lifetime
-
1946
- 1946-03-12 FR FR926608D patent/FR926608A/en not_active Expired
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1753659A (en) * | 1926-05-13 | 1930-04-08 | Vaman R Kokatnur | Anhydrous soap gels and method of making same |
US2350906A (en) * | 1938-05-20 | 1944-06-06 | Frank S Busser | Lubricant grease |
US2363013A (en) * | 1941-12-30 | 1944-11-21 | Standard Oil Dev Co | Stable lubricating composition |
US2390450A (en) * | 1942-01-22 | 1945-12-04 | Cities Service Oil Co | Lithium base greases |
US2383904A (en) * | 1942-08-12 | 1945-08-28 | Standard Oil Dev Co | Lubricant manufacture |
US2382531A (en) * | 1942-08-17 | 1945-08-14 | Auer Laszlo | Soap manufacture |
US2383906A (en) * | 1942-10-28 | 1945-08-28 | Standard Oil Dev Co | Improved manufacture |
US2351384A (en) * | 1942-11-18 | 1944-06-13 | Shell Dev | Lithium soap grease |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2576031A (en) * | 1948-10-30 | 1951-11-20 | Standard Oil Dev Co | Lubricating grease containing soaps of tall oil |
US2697693A (en) * | 1951-11-05 | 1954-12-21 | Standard Oil Co | Manufacture of lithium hydroxy carboxylic acid soap greases |
US2860151A (en) * | 1954-01-20 | 1958-11-11 | Lamson Edward Robert | Method for the manufacture of soap |
US2898298A (en) * | 1954-03-16 | 1959-08-04 | Sinclair Refining Co | Process for lithium base grease |
US2888402A (en) * | 1954-04-07 | 1959-05-26 | Exxon Research Engineering Co | Process for preparing lubricating greases |
US2801220A (en) * | 1954-07-06 | 1957-07-30 | Baker Castor Oil Co | Production of lubricating greases from monohydric alcohol esters of hydroxy fatty acids |
US2959548A (en) * | 1955-11-25 | 1960-11-08 | Exxon Research Engineering Co | Process for forming a lithium-calcium grease composition |
US2929781A (en) * | 1956-04-18 | 1960-03-22 | Exxon Research Engineering Co | Process for making a lithium-calcium base grease |
Also Published As
Publication number | Publication date |
---|---|
GB583303A (en) | 1946-12-13 |
FR926608A (en) | 1947-10-07 |
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