US2370300A - Lubricant - Google Patents
Lubricant Download PDFInfo
- Publication number
- US2370300A US2370300A US380709A US38070941A US2370300A US 2370300 A US2370300 A US 2370300A US 380709 A US380709 A US 380709A US 38070941 A US38070941 A US 38070941A US 2370300 A US2370300 A US 2370300A
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- Prior art keywords
- esters
- friction
- alcohol
- alcohols
- tartrate
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- 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
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
-
- 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
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/102—Aliphatic fractions
-
- 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
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic 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
- C10M2207/28—Esters
- C10M2207/287—Partial esters
-
- 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
- C10M2207/28—Esters
- C10M2207/287—Partial esters
- C10M2207/289—Partial esters containing free hydroxy groups
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- 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
- C10M2207/28—Esters
- C10M2207/34—Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
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- 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
- C10M2207/40—Fatty vegetable or animal oils
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- 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
- C10M2207/40—Fatty vegetable or animal oils
- C10M2207/402—Castor oils
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- 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
- C10M2207/40—Fatty vegetable or animal oils
- C10M2207/404—Fatty vegetable or animal oils obtained from genetically modified species
-
- 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
- C10N2010/06—Groups 3 or 13
-
- 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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/02—Bearings
-
- 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
Definitions
- This invention relates to a compounded lubricant.
- the present application is a division of my application Serial No. 177,878, filed December 3, 1937, on Composition of matter and process of lubrication.
- Material reduction of friction at low speeds is a severe requirement of compounded lubricatin oils, particularly when the metal surfaces to be lubricated are cast iron on cast iron, steel on steel, or other pairs of ferrous metal surfaces.
- Another object of the invention is to provide a lubricating composition which is especially effective for reducing friction between ferrous metal frictional surfaces moving at low speeds relative to one another.
- a further object of the invention is to provide a new composition ofmatter comprising esters of alcohols naturally occurring in sperm oil.
- the drawing is a graphical representation of experimental results which show the discoveries embodied in this invention.
- R1 may be hydrogen or an alkyl group; R2 comprises a long carbon chain.
- acids having either an alpha or beta or both alpha and beta hydroxyl groups are:
- Glycolic acid CH2 OH COOH
- An essential characteristic of the compounds of this invention is that the alcoholic portion of the ester must comprise a long carbon chain.
- the following are alcohols having a. long carbon chain:
- Decyl alcohol CmI-InOH.
- Dodecyl alcohol, CmHaOH Tetradecyl alcohol CuHaOH Cetyl alcohol, CrsHsaOH Octadecyl alcohol, CnHmOH Ceryl alcohol, CzaHsaOH Myricyl alcohol, CaoHuO Lanolin alcohol, CuHaaO Oleyl alcohol, CraHJsOH Lorol, a material containing lauryl alcohol and sold by E. I. du Pont de Nemours, is a satisfactory source of long chain alcohols.
- Esters of any of the above types of acids in combination with any of the above listed 10118 chain alcohols are regarded as falling within the broad scope of this invention.
- myricyl tartrate, oleyl tartrate and lanolin tartrate may be used.
- decyl lactate dodecyl lactate, tetradecyl lactate, cetyl lactate, lauryl lactate, octadecyl lactate, ceryl lactate, myricyl lactate, oleyl lactate and lanolin lactate are encompassed in the broad scope of the invention.
- esters are prepared from the respective acids and alcohols by the usual esterification reaction:
- the reaction may be efiected by heating the two constituents and vaporizing the water formed.
- Dehydration agents such as sulfuric acid may also be utilized to promote the reaction.
- the invention also embodies one species of ester having definitely superior merit as compared with other members of the above described genus.
- This species is believed to be a new composition of matter which possesses utility for purposes other than a compounding ingredient in lubricating oils.
- the compound comprises the ester of an hydroxy acid, such as previously described, and the alcohols obtained from sperm oil.
- sperm oil comprises esters of several long chain alcohols and hydrolysis of the oil yields a mixture of these alcohols together with fatty acids.
- the acids and alcohols may be separated by converting the acids to soaps and separating the soaps and alcohols by distillation or extraction with solvents by processes well known in the art.
- the mixture of long chain alcohols so obtained is termed spermol in the present specification.
- the exact chemical formulae and relative proportions of the alcohol ingredients of spermol have not been ascertained, but it is said that sperm oil contains alcohols such as cetyl and octadecyl in minor proportions and an alcohol of the type of oleyl in larger proportions. It is to be noted that sperm oil is not the equivalent of spermol," since the former is a naturally-occurring oil and the latter comprises the natural mixture of alcohols obtained by hydrolysis of the oil.
- SpermoP esters of hydroxy acids are especially eifective for reducing friction between ferrous metal surfaces at low speeds.
- Esters of spermoP' are decidedly superior to esters of various other long chain alcohols falling within the broader scope of the invention. This fact is illustrated by data showing .5% of "spermol" tartrate to be apprcximately as effective inreducing friction as 1% of lauryl tartrate. In other words, it takes approximately half as much addition agent to obtain the same reduction in friction when spermol esters are used as is required when esters of other long chain alcohols, exemplified by lauryl alcohol, are added.
- the proportions of the addition agent which may be incorporated in lubricating oils may vary over a considerable range. Measurable improvements are obtained with as little as 0.1% of the ester, but it is preferred to add from .5 to 1.5% by weight of the compound. Because the esters are expensive ingredients, it is generally not desirable to add more than about 2% to the lubricants, although as much as 10% or more may be permissible for various purposes.
- esters of this invention maybe utilized in mineral lubricating oils of all types, and it should be understood that the term lubricating oil includes highly naphthenic lubricants such as are obtained from California crude oils or highly paramnic lubricants obtained by solvent refining processes or from Pennsylvania type crudes. Likewise, the addition agent will be of utilityin oils of widely difi'erent viscosities, ranging from light spindle oils through the usual range of viscosities utilized in ordinary internal combustion engines to the highly viscous oils manufactured for gears or heavy machinery.
- the generic aspect of this invention includes highly thickened oils, such as castor machine oils containing aluminum naphthenate, or other known thickening agents.
- the invention also includes grease compositions containing soaps of the alkali and/or heavy metals within its generic scope. It will be apparent that numerous modifications and variations of the illustrated examples may be utilized in the practice of the invention which is of the scope of the following claims.
- a compounded lubricant comprising a hydrocarbon lubricating oil and a small amount of tartaric acid ester of an aliphatic alcohol having from approximately ten to approximately thirty carbon atoms in the chain, the proportion of said ester being sufflcient to effectively decrease the coemcient of friction between metal frictional surfaces at low rubbing speeds.
- a compounded lubricant comprising a hydrocarbon lubricating oil and from approximately 0.1% to approximately 10% by weight based on the oil of a tartaric acid ester of an aliphatic alcohol having from approximately ten to approximately thirty carbon atoms in the chain.
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- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Description
Feb. 27, 1945. B. FARRINGTON 2,370,300
LUBRICANT Original Filed Dec. 3, 1937 I5 3O 4O 5O SPEED FT. PER MINUTE KINETIC OILINESS TESTING MACHINE(PAT.N0.2,020,565)
Surfacesz- Casr Iron on Casi Iron Temperarure:- 275 F. Loading I500 lbs./sqin.'
IN VENTORS Bruce 8. Farr/fig for;
Patented Feb. 27, 1945 UNITED STATES LUBRICANT Bruce B. Farrington, Berkeley, Calif., assignor to Standard Oil Company of California, San Francisco, Calif., a corporation of Delaware Original application December 3, 1937, Serial No. 177,878. Divided and this application February 26, 1941, Serial No. 380,709
2 Claims.
This invention relates to a compounded lubricant. The present application is a division of my application Serial No. 177,878, filed December 3, 1937, on Composition of matter and process of lubrication.
A large number of addition agents have been proposed to improve the lubricating action of mineral oils b w 1 th fllcient of friction between metal surfaces to a greater ex e is obtainable with mineral oils alone. The actio of these addition agents is in general quite specific and for the most part unpredictable. An addition agent which is effective to reduce friction between one pair of metals at high speeds will often be found ineffective to reduce the friction between the same pair of metals at low speeds. In other words, the phenomenon of lubrication and reduction of friction is not yet well understood and developments in this field are largely empirical. It is therefore apparent that the actual conditions of operation encountered in any particular mechanism must be examined critically if the addition agent is to be truly beneficial.
The lubrication of reciprocating parts necesthe reciprocating element decelerates to and accelerates from zero speed ,at each end f thestroke. Since reciprocating parts are common in all types of machinery, reduction of friction at low speeds approaching zero is of great importance as a lubricating problem. The necessity for adequate lubrication at low speeds is illustrated by the fact that the maximum wear of the cylinder walls of an internal combustion engine occurs at the upper limit of the piston ring travel where the rubbing speed i low and where ordinary lubricants fail to reduce friction or wear to the same extent as it is reduced in the remaining portion of the piston travel.
Material reduction of friction at low speeds is a severe requirement of compounded lubricatin oils, particularly when the metal surfaces to be lubricated are cast iron on cast iron, steel on steel, or other pairs of ferrous metal surfaces. It
has been observed that most oiliness agents which 45 have been proposed by the prior art fail to materially benefit the action of mineral oils in reducing friction under these extreme conditions.
Accordingly, it is an object of this invention to provide a process for effectively reducing friction at extremely low rubbing speeds between ferrous metal frictional surfaces.
Another object of the invention is to provide a lubricating composition which is especially effective for reducing friction between ferrous metal frictional surfaces moving at low speeds relative to one another.
A further object of the invention is to provide a new composition ofmatter comprising esters of alcohols naturally occurring in sperm oil.
The drawing is a graphical representation of experimental results which show the discoveries embodied in this invention.
A certain class of compounds has been found to 5 possess unpredictable and outstanding properties 10 of a particular type and may be illustrated by the following examples:
Alpha hydrozv esters Beta hudrory esters H H Ih---C-O- R-l oi t t In these formulae R1 may be hydrogen or an alkyl group; R2 comprises a long carbon chain.
Examples of acids having either an alpha or beta or both alpha and beta hydroxyl groups are:
Tl' alic acid, (CHOH COOH) Tartronic acid, CHOH (COOH) Lactic acid, CH3 CHOH COOH 0 Citric acid, HOOC crncon coon cm coon Mucic acid, (CHOHM (COOH):
Glycolic acid, CH2 OH COOH An essential characteristic of the compounds of this invention is that the alcoholic portion of the ester must comprise a long carbon chain. The following are alcohols having a. long carbon chain:
Decyl alcohol, CmI-InOH. Dodecyl alcohol, CmHaOH Tetradecyl alcohol, CuHaOH Cetyl alcohol, CrsHsaOH Octadecyl alcohol, CnHmOH Ceryl alcohol, CzaHsaOH Myricyl alcohol, CaoHuO Lanolin alcohol, CuHaaO Oleyl alcohol, CraHJsOH Lorol, a material containing lauryl alcohol and sold by E. I. du Pont de Nemours, is a satisfactory source of long chain alcohols.
Esters of any of the above types of acids in combination with any of the above listed 10118 chain alcohols are regarded as falling within the broad scope of this invention. For example, dec 1 tartrate, dodecyl tartrate, tetradecyl tartra. cefyl tartrate, lauryl tartrate, octadecyl tartrate. ceryl tartrate. myricyl tartrate, oleyl tartrate and lanolin tartrate may be used. Simitxamm larly, decyl lactate, dodecyl lactate, tetradecyl lactate, cetyl lactate, lauryl lactate, octadecyl lactate, ceryl lactate, myricyl lactate, oleyl lactate and lanolin lactate are encompassed in the broad scope of the invention.
These esters are prepared from the respective acids and alcohols by the usual esterification reaction:
The reaction may be efiected by heating the two constituents and vaporizing the water formed. Dehydration agents such as sulfuric acid may also be utilized to promote the reaction.
The invention also embodies one species of ester having definitely superior merit as compared with other members of the above described genus. This species is believed to be a new composition of matter which possesses utility for purposes other than a compounding ingredient in lubricating oils. The compound comprises the ester of an hydroxy acid, such as previously described, and the alcohols obtained from sperm oil.
Sperm oil comprises esters of several long chain alcohols and hydrolysis of the oil yields a mixture of these alcohols together with fatty acids. The acids and alcohols may be separated by converting the acids to soaps and separating the soaps and alcohols by distillation or extraction with solvents by processes well known in the art. The mixture of long chain alcohols so obtained is termed spermol in the present specification. The exact chemical formulae and relative proportions of the alcohol ingredients of spermol have not been ascertained, but it is said that sperm oil contains alcohols such as cetyl and octadecyl in minor proportions and an alcohol of the type of oleyl in larger proportions. It is to be noted that sperm oil is not the equivalent of spermol," since the former is a naturally-occurring oil and the latter comprises the natural mixture of alcohols obtained by hydrolysis of the oil.
SpermoP esters of hydroxy acids are especially eifective for reducing friction between ferrous metal surfaces at low speeds.
In order to illustrate the effectiveness of the process and the compositions of this invention, a series of tests was run in a kinetic oiliness testing machine of the type disclosed in United States Patent No. 2,020,565, granted to Neely et al November 12, 1935. The data from these tests are shown graphically in ,the drawing. Attention is directed to the fact that esters of shorter chain alcohols are not effective in reducing friction between cast iron surfaces at low speeds. This is illustrated by the curve showing the coeflicient of friction at various speeds of an oil containin 1% diamyl tartrate.
Esters of spermoP' are decidedly superior to esters of various other long chain alcohols falling within the broader scope of the invention. This fact is illustrated by data showing .5% of "spermol" tartrate to be apprcximately as effective inreducing friction as 1% of lauryl tartrate. In other words, it takes approximately half as much addition agent to obtain the same reduction in friction when spermol esters are used as is required when esters of other long chain alcohols, exemplified by lauryl alcohol, are added.
Experiments indicate that spermol esters of alpha and beta hydroxy acids other than tar tarlc are eflective addition agents for lubricating oils.
The proportions of the addition agent which may be incorporated in lubricating oils may vary over a considerable range. Measurable improvements are obtained with as little as 0.1% of the ester, but it is preferred to add from .5 to 1.5% by weight of the compound. Because the esters are expensive ingredients, it is generally not desirable to add more than about 2% to the lubricants, although as much as 10% or more may be permissible for various purposes.
The esters of this invention maybe utilized in mineral lubricating oils of all types, and it should be understood that the term lubricating oil includes highly naphthenic lubricants such as are obtained from California crude oils or highly paramnic lubricants obtained by solvent refining processes or from Pennsylvania type crudes. Likewise, the addition agent will be of utilityin oils of widely difi'erent viscosities, ranging from light spindle oils through the usual range of viscosities utilized in ordinary internal combustion engines to the highly viscous oils manufactured for gears or heavy machinery.
The discoveries disclosed hereinabove are utilized in the process of this invention by lubricating ferrous metal surfaces, such as cast iron on cast iron, moving in frictional contact at low speeds relative to each other with a film of lubricating oil and adding an alpha or beta hydroxy ester of long chain alcohols to the lubricant in order to reduce the coemcient of friction.
This process is not merely a mechanical one but involves chemical or physico-chemical action, since the added esters are present in a proportion so small that they have no appreciable effect on the viscosity or mere mechanical action of the lubricant. The reduction of friction effected by the esters is probably due to their chemical action on the metal surfaces being lubricated, although the esters may also act on the base oil itself in some unknown chemical manner and thereby contribute to the improved lubricating action.
Specific embodiments of the invention have been described but this has been done by way of illustration only and with the intention that the scope of the invention should not be limited thereby. For example, the generic aspect of this invention includes highly thickened oils, such as castor machine oils containing aluminum naphthenate, or other known thickening agents. The invention also includes grease compositions containing soaps of the alkali and/or heavy metals within its generic scope. It will be apparent that numerous modifications and variations of the illustrated examples may be utilized in the practice of the invention which is of the scope of the following claims.
I claim:
1. A compounded lubricant comprising a hydrocarbon lubricating oil and a small amount of tartaric acid ester of an aliphatic alcohol having from approximately ten to approximately thirty carbon atoms in the chain, the proportion of said ester being sufflcient to effectively decrease the coemcient of friction between metal frictional surfaces at low rubbing speeds.
2. A compounded lubricant comprising a hydrocarbon lubricating oil and from approximately 0.1% to approximately 10% by weight based on the oil of a tartaric acid ester of an aliphatic alcohol having from approximately ten to approximately thirty carbon atoms in the chain.
BRUCE B. FARRINGTON.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US380709A US2370300A (en) | 1937-12-03 | 1941-02-26 | Lubricant |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US17787837A | 1937-12-03 | 1937-12-03 | |
US380709A US2370300A (en) | 1937-12-03 | 1941-02-26 | Lubricant |
US380708A US2370299A (en) | 1941-02-26 | 1941-02-26 | Compounded lubricant |
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US2370300A true US2370300A (en) | 1945-02-27 |
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US380709A Expired - Lifetime US2370300A (en) | 1937-12-03 | 1941-02-26 | Lubricant |
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Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2436272A (en) * | 1945-02-27 | 1948-02-17 | Socony Vacuum Oil Co Inc | Mineral oil composition |
US2441023A (en) * | 1945-01-26 | 1948-05-04 | Shell Dev | Lubricating oil compositions containing polymerized allyl esters of carboxylic acids |
US2443579A (en) * | 1944-10-13 | 1948-06-15 | Socony Vacuum Oil Co Inc | Mineral oil composition |
US2443578A (en) * | 1944-10-13 | 1948-06-15 | Socony Vacuum Oil Co Inc | Mineral oil composition |
US2628941A (en) * | 1950-02-04 | 1953-02-17 | Shell Dev | Extreme pressure lubricant |
US2755250A (en) * | 1955-03-28 | 1956-07-17 | Shell Dev | Extreme pressure lubricant |
US4091131A (en) * | 1975-09-19 | 1978-05-23 | Bethlehem Steel Corporation | Nonperishable direct enameling steel and method for producing same |
US4108784A (en) * | 1974-04-09 | 1978-08-22 | The Lubrizol Corporation | Hydroxyalkyl hydroxy-aromatic condensation products as fuel and lubricant additives |
US4176077A (en) * | 1974-04-09 | 1979-11-27 | The Lubrizol Corporation | Haloalkyl hydroxy-aromatic condensation products as lubricant additives |
US4205960A (en) * | 1974-04-09 | 1980-06-03 | The Lubrizol Corporation | Hydroxyalkyl hydroxy-aromatic condensation products as fuel and lubricant additives |
US4285824A (en) * | 1979-01-22 | 1981-08-25 | The Lubrizol Corporation | Hydroxyalkyl hydroxy-aromatic condensation products as fuel and lubricant additives |
US4343740A (en) * | 1980-02-22 | 1982-08-10 | The Lubrizol Corporation | Hydroxylalkyl hydroxy-aromatic condensation products as fuel and lubricant additives |
USRE31349E (en) * | 1972-03-10 | 1983-08-16 | National Steel Corporation | Lubricated metallic container stocks and method of preparing the same and applying organic coating thereto |
-
1941
- 1941-02-26 US US380709A patent/US2370300A/en not_active Expired - Lifetime
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2443579A (en) * | 1944-10-13 | 1948-06-15 | Socony Vacuum Oil Co Inc | Mineral oil composition |
US2443578A (en) * | 1944-10-13 | 1948-06-15 | Socony Vacuum Oil Co Inc | Mineral oil composition |
US2441023A (en) * | 1945-01-26 | 1948-05-04 | Shell Dev | Lubricating oil compositions containing polymerized allyl esters of carboxylic acids |
US2436272A (en) * | 1945-02-27 | 1948-02-17 | Socony Vacuum Oil Co Inc | Mineral oil composition |
US2628941A (en) * | 1950-02-04 | 1953-02-17 | Shell Dev | Extreme pressure lubricant |
US2755250A (en) * | 1955-03-28 | 1956-07-17 | Shell Dev | Extreme pressure lubricant |
USRE31349E (en) * | 1972-03-10 | 1983-08-16 | National Steel Corporation | Lubricated metallic container stocks and method of preparing the same and applying organic coating thereto |
US4176077A (en) * | 1974-04-09 | 1979-11-27 | The Lubrizol Corporation | Haloalkyl hydroxy-aromatic condensation products as lubricant additives |
US4163730A (en) * | 1974-04-09 | 1979-08-07 | The Lubrizol Corporation | Hydroxyalkyl hydroxy-aromatic condensation products as lubricant additives |
US4108784A (en) * | 1974-04-09 | 1978-08-22 | The Lubrizol Corporation | Hydroxyalkyl hydroxy-aromatic condensation products as fuel and lubricant additives |
US4205960A (en) * | 1974-04-09 | 1980-06-03 | The Lubrizol Corporation | Hydroxyalkyl hydroxy-aromatic condensation products as fuel and lubricant additives |
US4091131A (en) * | 1975-09-19 | 1978-05-23 | Bethlehem Steel Corporation | Nonperishable direct enameling steel and method for producing same |
US4285824A (en) * | 1979-01-22 | 1981-08-25 | The Lubrizol Corporation | Hydroxyalkyl hydroxy-aromatic condensation products as fuel and lubricant additives |
US4343740A (en) * | 1980-02-22 | 1982-08-10 | The Lubrizol Corporation | Hydroxylalkyl hydroxy-aromatic condensation products as fuel and lubricant additives |
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