US2418358A - Lubricating oil - Google Patents

Lubricating oil Download PDF

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US2418358A
US2418358A US419990A US41999041A US2418358A US 2418358 A US2418358 A US 2418358A US 419990 A US419990 A US 419990A US 41999041 A US41999041 A US 41999041A US 2418358 A US2418358 A US 2418358A
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Prior art keywords
lubricant
compounds
boron
hydrocarbon
lubricants
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US419990A
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Bert H Lincoln
Gordon D Byrkit
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ConocoPhillips Co
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Continental Oil Co
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M1/00Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
    • C10M1/08Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/16Paraffin waxes; Petrolatum, e.g. slack wax
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/04Ethers; Acetals; Ortho-esters; Ortho-carbonates
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/04Ethers; Acetals; Ortho-esters; Ortho-carbonates
    • C10M2207/044Cyclic ethers having four or more ring atoms, e.g. furans, dioxolanes
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/281Esters of (cyclo)aliphatic monocarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/282Esters of (cyclo)aliphatic oolycarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/283Esters of polyhydroxy compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/286Esters of polymerised unsaturated acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2227/00Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
    • C10M2227/08Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions having metal-to-carbon bonds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/06Groups 3 or 13
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/04Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/04Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
    • C10N2040/042Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for automatic transmissions
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/04Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
    • C10N2040/044Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for manual transmissions
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/04Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
    • C10N2040/046Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for traction drives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2060/00Chemical after-treatment of the constituents of the lubricating composition
    • C10N2060/04Oxidation, e.g. ozonisation

Definitions

  • the product of our invention has the very important property of reacting with the metal surfaces, penetrating or adsorbing on the metal, and leaving a film of lubricant with high oiliness character which remains on the metal surfac irrespective of the length of time the machine is idle.
  • This high oiliness film is very even and results in smooth operation, which may be easily discerned by the experienced operator and lubricating engineer.
  • One objezt of our invention is to provlde a lubricating composition having improved filmstrength and extreme-pressure characteristics.
  • a regimentation or cybotaxis of the molecules will take place in the adsorbed film, the molecules being oriented with respect to the surface of the metal by which they are adsorbed.
  • the films of polar compounds, adsorbed by a metal can be plainly seen and th orientation of the polar molecules on the metalv surface ascertained by can be recorded photographlcally. The X-ray photographs will clearly show the orientation of the molecules by characteristic pictures.
  • hydrocarbon portion of our lubricant may be comparatively viscous or nonviscous, refined or unrefined, natural or synthetic.
  • any hydrocarbon oil may be used within the scope of our invention.
  • boron compounds which contain certain other inorganic elements such as halogen. nitrogen, oxygen, sulfur, phosphorus, metals, etc.
  • the boron compounds particularly suited to our invention are of two classes, as follows:
  • RzBOR in which R and Rare organic radicals at least one of which contains a carboxylic ester group, -COzR, and at least one of the said R and R contains one or more substituents, said substituents being atoms or combination of atoms inorganic or inorganic radicals, selected from the group of halogen, nitrogen, sulfur, phospnorus, oxygen, metals, etc.
  • R and R are organic radicals, at least one of which contains a carboxylic ester group, CO2R", and at least one of which contains one or more substituents, said substituents being atoms or combinations of atoms in organic or inorganic radicals, selected from the group of halogen, nitrogen, sulfur, phosphorus, oxygen, metals, etc.
  • substituted organo-boron esters have the general formula 'at least one carbo-boron bond and at least one organic radical is removable by saponification.
  • organo-boron esters to which we add substituents from the group set out in the next preceding paragraph to produce the compounds that are added to hydrocarbon oil to form new compositions of matter which comprise the present invention, are described in our copending application, Serial 330,950, filed April 22, 1940.
  • organo-boron esters .that contain a carboxylic ester group in an organic radical are superior to the less complex organo-boron esters.
  • desirable characteristics of our organo-boron esters containing carboxylic ester groups are appreciably improved by chemically incorporating a radical made up of or containing an atom or atoms from the group hereinabove set forth.
  • the film strength of the blend made up of hydrocarbon oil and a small quantity of our substituted organsboron ester is higher than that of a. similar blend in which the addition agent is an organo-boron ester containing no substituted atoms from the group we have tried and tested and herein claim.
  • the addition agents of our invention impart to a hydrocarbon oil a.
  • lubricants prepared by adding even minute quantities of the products within the ambit of our invention prevent or greatly reduce the deterioration of the 011 while it is stored or while it is in use.
  • the lubricants produced by blending a hydrocarbon oil and our additives are especially suitable for use in crankcases of modern internal combustion engines and Diesel engines. Their stability, film-strength, noncorrosiveness, and particularly oiliness characteristics designate them as very efiective and emclent lubricants for all rubbing surfaces requiring a lubricant with a viscosity that may be obtained in a blend made up of hydrocarbon oil and our addition agents.
  • CEHIIB(OCHZCOSC5HI1)2 Di-thiocarboxyamylmethyl amylborate C5H11B(OCH2P(C5H11) 2) 2 Di(bis-amylphosphinomethol) amylborate I C5H11B(OCH2N(C5H11)2) 2 Di(bis-amylam inomethyl) amylborate C5H11B(OCH2CO2)2Ca Calcium di(carboxymethyl) amylborate CsHuB OC24H4sCl) 2 Di(chlorotetracosyl) amylborate III.
  • 5 ester containing organo-boron compounds may be more effective in some proportions if a small amount of halogen-free, oxygen-containing carbon compound is included in the composition.
  • the oxygen-containing carbon compound may be of aliphatic, aromatic, or hetero-cyclic nature and may be blended with the substituted organoboron compound in amounts ranging from 5 to 50 per cent.
  • Such compounds include esters of oxidized petroleum hydrocarbons such as wax, methyl ricinoleate, diphenyl ether, diphenylene oxide (dibenzofuran), and many others.
  • sludge forming compounds of a boron compound selected from the class consisting of compounds 7 having the general formulas RzBOR' and 2.
  • a lubricant comprising in combination a major proportion of hydrocarbon oil and a minor iroportion, suilicient to stabilize the oil against 'ormation of corrosive oxidation products or :ludge forming compounds, of a boron compound :elected from the class consisting of compounds raving the general formulas RaBOR' and 313(0R): in which R and R are organic radi- :als, at least one of which contains a carboxylic aster group, and at least one of which contains phosphorus.
  • a lubricant comprising in combination a najor proportion of hydrocarbon oil and a minor proportion, sufl'icient to stabilize the oil against formation of corrosive oxidation products or RB(OR') a in which R and R are organic radicals, at least one of which contains a carboxylic ester group, 5 1d at least one of which is sulphur hearing.
  • a lubricant comprising in combination a major proportion of hydrocarbon oil and a minor proportion, suflicient to to stabilize the oil against formation of corrosive oxidation products or sludge forming compounds, of thiocarboxvamylmethyl amylborate.

Description

AT EN 1 FFlCE LUBRICATING OIL Bert H. Lincoln and Gordon D. Byrklt, Ponca City, Okla., assignors to Continental Oil Company, Ponca City, Okla., a corporation of Delaware No Drawing. Application November 21, 1941 Serial No. 419,990
4 Claims.
specifically comprises such products as new com-.
positions of matter.
This is a continuation in part of our copending application, Serial No. 330,950, filed April 22, 1940.
Present-day mechanical devices require lubricating oils of high film strength and of high oiliness characteristics. It has been found that the present-day hydrocarbon lubricants of the very highest quality are deficient in these two very important characteristics. These two properties are of vital importance under conditions of thin film lubrization where the lubricant has been squeezed between th friction surfaces because of high pressure, slow speeds, and other causes. It is readily seen that the viscosity or the body of the lubricant plays no part in this type of lubrication and that the remaining film of oil should tend to keep the coefficient of friction as low as possible and must have a very high film strength and be of high oiliness value to prevent rupture of the film of the lubricant which would cause seizure.
Mechanical devices are being designed for higher pressure operation, and the film strength of the best quality straight hydrocarbon lubricants has been found to be too low and not sufficient; therefore an invention which provides the means of improving the film strength of these lubricants is of great importance to the art of lubricant manufacture and to the designer and fabricator of mechanical devices,
Substantially all machines operate in part or at times totally under conditions of thin film lubrication, under which conditions the oiliness or unctuosity of th lubricant is the first and primary requisite of efficient operation. Those skilled in the art of lubricant manufacture or machine manufacture will readily appreciate the value of an invention that will improve the-oiliness of these otherwise high quality lubricants. Unde some conditions, a very small amount of an addition agent will stabilize a hydrocarbon oil against formation of corrosive oxidation products or sludge forming compounds; and as little as 0.001 per cent is often sufficient.
In starting idle mechanical equipment which is lubricated from a sump by pumping or circulating the lubricant, there is always a short period of time during which the rubbing surfaces must operate under conditions of dry friction if ordinary hydrocarbon lubricants are used. With dry friction. the wear on friction surfaces is extreme; and during cold weather when the lubricant is sluggish or during periods when the lubricating system is not functioning properly for one reason or another, rubbing surfaces may not only suffer considerable wear but may bedamaged to the point where they must be replaced. The product of our invention has the very important property of reacting with the metal surfaces, penetrating or adsorbing on the metal, and leaving a film of lubricant with high oiliness character which remains on the metal surfac irrespective of the length of time the machine is idle.
This high oiliness film is very even and results in smooth operation, which may be easily discerned by the experienced operator and lubricating engineer.
When the hydrocarbon lubricants are diluted with unburned fuel or with other light hydrocarbons, this small degree of oiliness of the original hydrocarbon lubricant is greatly decreased. We have found that the addition of the product of our invention to hydrocarbon lubricants more than compensates for the loss of oiliness and load-carrying ability by dilution.
One objezt of our invention is to provlde a lubricating composition having improved filmstrength and extreme-pressure characteristics.
Other and further objects of our invention will appear from the following description:
We have found that certain compounds are adsorbed or absorbed by metals forming a plurality of layers or films on the surface of the metal, which films are very tenacious (they have a high film strength) and have the property of reducing the coefiicient of friction to a marked degree. The compounds which are most readily absorbed by metals are ones consisting of polar molecules, that is, molecules of unsymmetrical electrical character which contain an atom or group of atoms exhibiting a secondary or residual valence. These polar compounds tend to produce regimentation of the molecules of hydrocarbon oil when added thereto. If a metal is immersed in a strongly polar compound, a regimentation or cybotaxis of the molecules will take place in the adsorbed film, the molecules being oriented with respect to the surface of the metal by which they are adsorbed. The films of polar compounds, adsorbed by a metal, can be plainly seen and th orientation of the polar molecules on the metalv surface ascertained by can be recorded photographlcally. The X-ray photographs will clearly show the orientation of the molecules by characteristic pictures.
The X-ray investigation has shown that strongly polar molecules form adsorbed films of we use from 0.1 to 2 per cent of the organic boron compound in the hydrocarbon oil. For other purposes, we us from 0.001 to 0.1 per cent of the organic boron compound in a lubricant. The
hydrocarbon portion of our lubricant may be comparatively viscous or nonviscous, refined or unrefined, natural or synthetic. In other words, any hydrocarbon oil may be used within the scope of our invention.
In practicing our invention, we use certain organic boron compounds which contain certain other inorganic elements such as halogen. nitrogen, oxygen, sulfur, phosphorus, metals, etc. The boron compounds particularly suited to our invention are of two classes, as follows:
RzBOR, in which R and Rare organic radicals at least one of which contains a carboxylic ester group, -COzR, and at least one of the said R and R contains one or more substituents, said substituents being atoms or combination of atoms inorganic or inorganic radicals, selected from the group of halogen, nitrogen, sulfur, phospnorus, oxygen, metals, etc.
RB (CR 2. in which R and R are organic radicals, at least one of which contains a carboxylic ester group, CO2R", and at least one of which contains one or more substituents, said substituents being atoms or combinations of atoms in organic or inorganic radicals, selected from the group of halogen, nitrogen, sulfur, phosphorus, oxygen, metals, etc.
These two types of substituted organo-boron esters have the general formula 'at least one carbo-boron bond and at least one organic radical is removable by saponification.
The organo-boron esters, to which we add substituents from the group set out in the next preceding paragraph to produce the compounds that are added to hydrocarbon oil to form new compositions of matter which comprise the present invention, are described in our copending application, Serial 330,950, filed April 22, 1940.
I We have found that the organo-boron esters .that contain a carboxylic ester group in an organic radical are superior to the less complex organo-boron esters. We have found that the desirable characteristics of our organo-boron esters containing carboxylic ester groups are appreciably improved by chemically incorporating a radical made up of or containing an atom or atoms from the group hereinabove set forth. The film strength of the blend made up of hydrocarbon oil and a small quantity of our substituted organsboron ester is higher than that of a. similar blend in which the addition agent is an organo-boron ester containing no substituted atoms from the group we have tried and tested and herein claim. The addition agents of our invention impart to a hydrocarbon oil a. greater resistance tooxidation than do the organo-boron addition agents of the prior art; thus lubricants prepared by adding even minute quantities of the products within the ambit of our invention prevent or greatly reduce the deterioration of the 011 while it is stored or while it is in use. The lubricants produced by blending a hydrocarbon oil and our additives are especially suitable for use in crankcases of modern internal combustion engines and Diesel engines. Their stability, film-strength, noncorrosiveness, and particularly oiliness characteristics designate them as very efiective and emclent lubricants for all rubbing surfaces requiring a lubricant with a viscosity that may be obtained in a blend made up of hydrocarbon oil and our addition agents.
Examples of the compounds which we add to a hydrocarbon oil to produce new and improved lubricants are the following:
I. CEHIIB(OCHZCOSC5HI1)2 Di-thiocarboxyamylmethyl amylborate C5H11B(OCH2P(C5H11) 2) 2 Di(bis-amylphosphinomethol) amylborate I C5H11B(OCH2N(C5H11)2) 2 Di(bis-amylam inomethyl) amylborate C5H11B(OCH2CO2)2Ca Calcium di(carboxymethyl) amylborate CsHuB OC24H4sCl) 2 Di(chlorotetracosyl) amylborate III.
5 ester containing organo-boron compounds may be more effective in some proportions if a small amount of halogen-free, oxygen-containing carbon compound is included in the composition. The oxygen-containing carbon compound may be of aliphatic, aromatic, or hetero-cyclic nature and may be blended with the substituted organoboron compound in amounts ranging from 5 to 50 per cent. Such compounds include esters of oxidized petroleum hydrocarbons such as wax, methyl ricinoleate, diphenyl ether, diphenylene oxide (dibenzofuran), and many others.
It will be understood that certain features and sub-combinations are of utility and may be employed without reference to other features and suhcombinations. This is contemplated by and is within the scope of our claims. It is further obvious that various changes may be made in details within the scope of our claims without departing from the spirit of our invention. It is therefore to be understood that our invention is at to be limited to the specific details shown nd described.
Having thus described our invention, we claim:
1. A lubricant comprising in combination a iajor proportion of hydrocarbon oil and a minor roportion, sumcient to stabilize the oil against ormation of corrosive oxidation products or ludge forming compounds, of a boron compound elected from the class consisting of compounds laving the general formulas RQOR' and tB(OR')= in which R and R are organic radials, at least one of which contains a carboxvlic aster group.
sludge forming compounds. of a boron compound selected from the class consisting of compounds 7 having the general formulas RzBOR' and 2. A lubricant comprising in combination a major proportion of hydrocarbon oil and a minor iroportion, suilicient to stabilize the oil against 'ormation of corrosive oxidation products or :ludge forming compounds, of a boron compound :elected from the class consisting of compounds raving the general formulas RaBOR' and 313(0R): in which R and R are organic radi- :als, at least one of which contains a carboxylic aster group, and at least one of which contains phosphorus.
3. A lubricant comprising in combination a najor proportion of hydrocarbon oil and a minor proportion, sufl'icient to stabilize the oil against formation of corrosive oxidation products or RB(OR') a in which R and R are organic radicals, at least one of which contains a carboxylic ester group, 5 1d at least one of which is sulphur hearing.
4. A lubricant comprising in combination a major proportion of hydrocarbon oil and a minor proportion, suflicient to to stabilize the oil against formation of corrosive oxidation products or sludge forming compounds, of thiocarboxvamylmethyl amylborate.
BERT H. LINCOLN.
GORDON D. BYRKIT.
BCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 2,257,750 Lincoln et a1 Oct. 7, 1941 2,234,581 Rosen Mar. 11, 1941 2,181,915 Rosen Dec. 5, 1939 2,181,913 Rosen Dec. 5,1939 2,312,208 Clayton .Feb. 23, 1948 Lincoln et ai. Nov. 9, 1943
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2830953A (en) * 1956-05-28 1958-04-15 Gen Electric Silicone lubricating oils
US3177267A (en) * 1959-08-31 1965-04-06 Universal Oil Prod Co Retarding cracking of rubber due to ozone with a boron acid or borate ester
US3422016A (en) * 1964-05-15 1969-01-14 Universal Oil Prod Co Antioxidant mixture of boron ester of an alkanolamine and a hydroxyphenone,and use thereof

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2181913A (en) * 1934-04-07 1939-12-05 Standard Oil Dev Co Improved hydrocarbon composition
US2181915A (en) * 1939-04-25 1939-12-05 Standard Oil Dev Co Hydrocarbon composition
US2234581A (en) * 1937-09-30 1941-03-11 Standard Oil Dev Co Hydrocarbon composition containing organic boron compounds
US2257750A (en) * 1939-05-24 1941-10-07 Continental Oil Co Lubricating oil
US2312208A (en) * 1941-04-12 1943-02-23 Standard Oil Co California Compounded hydrocarbon oil
US2333871A (en) * 1941-04-10 1943-11-09 Continental Oil Co Lubricating oil

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2181913A (en) * 1934-04-07 1939-12-05 Standard Oil Dev Co Improved hydrocarbon composition
US2234581A (en) * 1937-09-30 1941-03-11 Standard Oil Dev Co Hydrocarbon composition containing organic boron compounds
US2181915A (en) * 1939-04-25 1939-12-05 Standard Oil Dev Co Hydrocarbon composition
US2257750A (en) * 1939-05-24 1941-10-07 Continental Oil Co Lubricating oil
US2333871A (en) * 1941-04-10 1943-11-09 Continental Oil Co Lubricating oil
US2312208A (en) * 1941-04-12 1943-02-23 Standard Oil Co California Compounded hydrocarbon oil

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2830953A (en) * 1956-05-28 1958-04-15 Gen Electric Silicone lubricating oils
US3177267A (en) * 1959-08-31 1965-04-06 Universal Oil Prod Co Retarding cracking of rubber due to ozone with a boron acid or borate ester
US3422016A (en) * 1964-05-15 1969-01-14 Universal Oil Prod Co Antioxidant mixture of boron ester of an alkanolamine and a hydroxyphenone,and use thereof

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