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US2901431A - Lubricating compositions - Google Patents

Lubricating compositions Download PDF

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Publication number
US2901431A
US2901431A US527648A US52764855A US2901431A US 2901431 A US2901431 A US 2901431A US 527648 A US527648 A US 527648A US 52764855 A US52764855 A US 52764855A US 2901431 A US2901431 A US 2901431A
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United States
Prior art keywords
oil
xanthate
asphalt
chlorine
mixture
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US527648A
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English (en)
Inventor
Harvey M Trowbridge
Harold A Woods
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Shell Development Co
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Shell Development Co
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Publication date
Priority to NL209632D priority Critical patent/NL209632A/xx
Priority to BE550174D priority patent/BE550174A/xx
Priority to NL97640D priority patent/NL97640C/xx
Application filed by Shell Development Co filed Critical Shell Development Co
Priority to US527648A priority patent/US2901431A/en
Priority to DEN12592A priority patent/DE1020750B/de
Priority to GB24304/56A priority patent/GB794688A/en
Priority to FR1158801D priority patent/FR1158801A/fr
Application granted granted Critical
Publication of US2901431A publication Critical patent/US2901431A/en
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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
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    • 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
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/08Inorganic acids or salts thereof
    • C10M2201/082Inorganic acids or salts thereof containing nitrogen
    • C10M2201/083Inorganic acids or salts thereof containing nitrogen nitrites
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    • 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
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
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    • 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
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/102Aliphatic fractions
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    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/108Residual fractions, e.g. bright stocks
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    • 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
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/026Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix 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
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/129Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/16Naphthenic acids
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/20Rosin acids
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    • 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
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    • 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
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/283Esters of polyhydroxy compounds
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/286Esters of polymerised unsaturated acids
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/287Partial esters
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    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/04Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen, halogen, and oxygen
    • C10M2211/044Acids; Salts or esters thereof
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    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/06Perfluorinated compounds
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/064Di- and triaryl amines
    • C10M2215/065Phenyl-Naphthyl amines
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    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/044Sulfonic acids, Derivatives thereof, e.g. neutral salts
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    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/06Thio-acids; Thiocyanates; Derivatives thereof
    • C10M2219/062Thio-acids; Thiocyanates; Derivatives thereof having carbon-to-sulfur double bonds
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    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
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    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • C10M2223/041Triaryl phosphates
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    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • C10M2223/042Metal salts thereof
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    • C10N2010/00Metal present as such or in compounds
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    • C10N2010/04Groups 2 or 12
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    • C10N2010/08Groups 4 or 14
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/02Bearings

Definitions

  • This invention relates to lubricants and more particularly to gear lubricants for use under extremely high pressure and over a Wide range of temperature conditions.
  • Lubricants of this type for semi-open or open gear lubrication must be viscous and they should be capable of carrying highloads at elevated temperatures. Such lubricants must have good adhesive properties so as not to be thrown olf the running gears. They must be water-resistant and they should be in a form which can be easily handled and applied.
  • An object of the present invention is to provide a lubricant having good high temperature and pressure properties. vide a lubricant of good adhesive properties over wide temperature conditions. Still another object of this invention is to provide a lubricant which is water-resistant and which is easy to use and apply. Other objects will become apparent from the detailed description of the invention.
  • a lubricant comprising (I) a major portion of a base mixture of substantial proportions each of a mineral oil of lubricating viscosity and an asphalt obtained from such sources as asphaltic base crudes and which is predominantly aromatic in character and (II) a minor portion of the combination of minor proportions each of three essential additives, namely: (1) an oil-soluble heavy metal soap, (2) an oil-soluble polyhalohydrocarbon thiocarbamate and (3) an oil-soluble ester of a high molecular weight aliphatic carboxylic acid and a low molecular weight monohydroxy alcohol.
  • the mineral oil component of the base (I) can be a liquid hydrocarbon of natural or synthetic origin and can range in viscosity from a light distillate mineral oil fraction to a heavy lubricating oil, such as gas oil, mineral lubricating oil, cylinder stock or Bright Stock or mixtures thereof. Mineral lubricating oils ranging in viscosity from 40 to 150 SSU at 210 F. are preferred.
  • the asphalt component of the base (I) can be obtained from various asphaltic crudes using various processes known to the art.
  • the preferred asphaltic bitumens are those which have softening points between about 100 F. and 250 F. and preferably between 100 F. and 150 F. and which are predominantly arohaving the properties given in Table 1.
  • Another object of the invention is to pro
  • One of the three essential additives incorporated in the compositions is an oil-soluble heavy metal salt or soap, of a cyclic carboxylic acid,,of an organic sulfonic acid, of a high molecular weight fatty acid and mixtures thereof, such as lead or zinc salts of cyclic carboxylic acids, such as naphthenic acid, abietic acid and other resin acids; of organic sulfonic acids, such as petroleum .sulfonic acids, and of higher fatty acids, such as oleic acid, stearic acid and the like; lead salts of cyclic carbloxylic acid, e.g., lead naphthenate represent a preferred c ass.
  • the naphthenic acids and their refined product can be prepared by the processes described in US. Patents 2,200,711, 2,214,438, 2,296,039 and 2,537,516.
  • the molecular weight of the naphthenic acid can vary from as low as about 200 to as high as about 1,000, while those which have molecular weights within the range of from 350 to 600 are particularly effective for attaining the objectives of this invention.
  • a second essential additive is an oil-soluble halohydrocarbon thiocarbonate ester, preferably a polychloroalkyl hydrocarbon thiocarbonate, which can be represented by the formula X Rcn-Rsc,
  • the Ys are S or O chalcogen atoms, at least one being a sulfur atom
  • the Xs are halogen atoms, preferably a middle halogen (chlorine or bromine: atomic number from 17 to 35), chlorine being particularly useful
  • n and m are whole numbers with their sum being at least 2
  • R and R are hydrocarbon radicals containing a total of at least 12 carbon atoms, at least one of them preferably being an aliphatic hydrocarbon radical of at least 10 carbon atoms, preferably from 12 to 30 carbon atoms and having at least two substituent halogen atoms
  • R is preferably a long-chain aliphatic radical.
  • halohydrocarbon thiocarbonate esters are suitably prepared by the reaction of polyhalohydrocarbons with less than the stoichiornetrically equivalent amount of an alkali or of an alkali earth metal organo thiocarbonate, with the formation of the alkali or alkali earth metal halide and the thiocarbonate full ester.
  • the thiocarbonate may be a mono-, dior tri-thiocarbonate.
  • various alkali or alkali metal organo thiocarbonates can be suitably used, such as the sodium, potassium, calciumand barium hydr0- carbon Xanthates and corresponding monoor tri-thiocarbonates.
  • Illustrative suitable substances are alkali metal lower alkyl xanthates, such as sodium methyl xanthate, potassium methyl xanthate, potassium ethyl xanthate, potassium butyl xanthate, sodium amyl Xanthate, and potassium amyl xanthate and alkali metal cule.
  • the thiocarbonateLester-salts are suitably reacted with various polyhaliogenated hydrocarbons in such proportions as to leave at least one halogen atom in the resulting thiocarbonate full ester.
  • the polyhalogenated hydrocarbons are preferably polych-lorinated aliphatic hydrocarbons of from about 2 to about 30 carbon atoms per mole- Mixtures of polychloroalkanes, including cyclic and acyclic alkanes, are particularly useful, giving products which are somewhat more compatible with the other components of the composition over a wider temperature range.
  • Polyhaloalkenes are also useful reactants. Some readily available materials which may be used are chlori- --nated naphtha, chlorinated paraflinic lubricating oil mixture of hydrocarbons, chlorinated paraffin wax and chlorinated rubber.
  • the reactants are reacted in proportions such that the final product contains both chlorine and thiocarbonate groups.
  • the amounts of chlorine and sulfur in the final product can vary over a wide range such as from about 25 to about 40% byv weight chlorine and from about 7 to about 15% sulfur.
  • Example I One hundred parts of 'chlornaphtha (chlorinated Stoddard solvent of 49% chlorine content) was reacted with 52 parts of potassium methyl xanthate (CH-,-O-CSSK), using acetone as a solvent .and following the same general procedure described above, except that the mixture was refluxed for one hour. 7
  • Example II Petroleum naphtha (Stoddard solvent) was chlorinated by bubbling chlorine gas therethrough until it contained about 52% 'by weight of chlorine. 225 parts by weight of the chlornaphtha was then admixed with about 400 content of about 10%, or a tri-thiocarbonate (divalent CS content of about 11.3%.
  • a third. essential additive is an oil-soluble ester of a high molecular, weight monocarboxylic acid and a low molecular weight alcohol.
  • Acids which can be used to form the esters include C to C fatty acids such as lauric, myristic, palmitic, stearic and oleic acids while the alcohols can be aliphatic monohydric alcohols such as methyl, ethyl, propyl, .butyl, hexyl and octyl alcohols,
  • the esters can be illustrated'by methyl propyl, butyl or octyl
  • the acetone was removed by 4 laurate, palmitate, stearate, oleate and mixtures thereof.
  • Preferred esters are methyl and/or butyl stearate.
  • compositions of this invention can be represented by:
  • composition of this invention is illustrated by the following example:
  • Examples of this invention include about 80 to 90% of a mixture of from 30 to 40% mineral oil and 60 to asphalt containing from about 3% to about 8% of lead rosinate, lead abietate, Zinc naphthenate and/or zinc abietate; from about 3% to about 7% additive of Example I or II or the reaction product of chlorinated petroleum naphtha and potassium ethyl xanthate 12% S, 35% C1), or the reaction product of chlorinated kerosene (40% Cl) and potassium isopropyl xanthate (10% S. 32% Cl) and mixtures thereof, and from about 0.5% to about 1.5% butyl ricinoleate, octyl palmitate and/or butyl chlorostearate.
  • compositions of this invention when tested in the Timken Lubricant Testing Machine (4 gram test procedure) described in the Lubricating Engineering, vol. 9, No. 6, 1953, page 295, indicated that they possess excellent load carrying capacity. Thus, Composition A of this invention when tested in this machine indicated excellent load carrying capacity after 480 minutes of testing.
  • Composition 1 6% Santopoid S and 94% of a mixture of 40% pale oil (.80 SSU at 210 F.) and 60% asphalt
  • Composition 2 (10% Pb naphthenate, 10% Santopoid S and 80% a mixture of 40% pale oil (80 SSU at 210 F.) and 60% asphalt)
  • Composition 6 (7% Pb naphthenate, 6% Santopoid S, 3% W001 grease alcohol and 84% of a mixture of 40% pale oil (80 SSU at 210 F.) and 60% asphalt)
  • Composition 7 (7% Pb naphthenate, 6% Santopoid S, 1% primary amine derived from coconut fatty acid and 86% of a mixture of 40% pale oil (80 SSU at 210 F.) and 60% asphalt)
  • Composition 8 (7% Pb naphthenate, 6% Santopoid S, 1% polyoxyethylene difatty acid and 86% of a mixture of 40% pale oil 80 SSU at 210 F.) and 60% asphalt);
  • compositions of this invention can be modified by addition thereto of minor amounts (0.011%) of antioxidants, corrosion inhibitors, extreme pressure agents, anti-wear agents and the like, such as alkyl phenols (2,6- ditertbutyl-4-methylphenol), amines, e.g., phenylnaphthylamine; organic phosphorus compounds, e.g., dilauryl 6 phosphate, dilauryl phosphite, tributyl phosphate, tricresyl phosphate; sodium nitrite, lithium nitrite, etc.
  • antioxidants such as alkyl phenols (2,6- ditertbutyl-4-methylphenol), amines, e.g., phenylnaphthylamine; organic phosphorus compounds, e.g., dilauryl 6 phosphate, dilauryl phosphite, tributyl phosphate, tricresyl phosphate
  • a lubricating composition comprising a major proportion of (I) a base mixture of from about to about of a mineral oil and from about 70 to about 60% of asphalt and having incorporated therein (II) from about 6% to about 10% oil-soluble lead naphthenate, from about 6% to about 8% of an oil-soluble polychlornaphtha xanthate containing from about 25% to about chlorine and from about 7% to about 15% sulfur in the molecule and from about 1% to about 2% butyl stearate.
  • a lubricating composition comprising a major proportion of a base mixture consisting essentially of 40% wt. mineral oil and wt. asphalt, about 7% wt. lead naphthenate, about 6% wt. polychlornaphtha xanthate containing about 30% wt. chlorine and about 10% wt. sulfur and about 1% wt. butyl stearate.

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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)
US527648A 1955-08-10 1955-08-10 Lubricating compositions Expired - Lifetime US2901431A (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
NL209632D NL209632A (xx) 1955-08-10
BE550174D BE550174A (xx) 1955-08-10
NL97640D NL97640C (xx) 1955-08-10
US527648A US2901431A (en) 1955-08-10 1955-08-10 Lubricating compositions
DEN12592A DE1020750B (de) 1955-08-10 1956-08-08 Schmiermittel
GB24304/56A GB794688A (en) 1955-08-10 1956-08-08 Lubricating compositions
FR1158801D FR1158801A (fr) 1955-08-10 1956-08-08 Compositions lubrifiantes

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Application Number Priority Date Filing Date Title
US527648A US2901431A (en) 1955-08-10 1955-08-10 Lubricating compositions

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US2901431A true US2901431A (en) 1959-08-25

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US (1) US2901431A (xx)
BE (1) BE550174A (xx)
DE (1) DE1020750B (xx)
FR (1) FR1158801A (xx)
GB (1) GB794688A (xx)
NL (2) NL209632A (xx)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3029203A (en) * 1959-10-06 1962-04-10 Gulf Research Development Co Wire rope lubricant

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL292095A (xx) * 1962-04-30
DE3026516A1 (de) * 1980-07-12 1982-02-11 Dieter 5060 Bergisch Gladbach Popp Heissgaserzeuger

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2210140A (en) * 1931-11-06 1940-08-06 Colbeth Ivor Milton Lubricant and process of producing it
US2292672A (en) * 1940-06-29 1942-08-11 Standard Oil Co Lubricant
US2331005A (en) * 1941-12-23 1943-10-05 Socony Vacuum Oil Co Inc Stabilized extreme pressure lubricant
US2516119A (en) * 1945-08-09 1950-07-25 Continental Oil Co Metal, phosphorus, and sulfur-containing organic compounds
US2607732A (en) * 1950-06-21 1952-08-19 Standard Oil Co Lubricants
US2607733A (en) * 1950-06-21 1952-08-19 Standard Oil Co Heavy duty lubricant
US2785130A (en) * 1953-12-21 1957-03-12 Texas Co Extreme pressure lubricant

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB519288A (en) * 1938-10-13 1940-03-20 Henry George Berger Extreme pressure lubricant
GB636118A (en) * 1946-10-08 1950-04-26 Standard Oil Dev Co Improvements in or relating to extreme pressure lubricants
US2638447A (en) * 1950-02-08 1953-05-12 Socony Vacuum Oil Co Inc Gear lubricant

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2210140A (en) * 1931-11-06 1940-08-06 Colbeth Ivor Milton Lubricant and process of producing it
US2292672A (en) * 1940-06-29 1942-08-11 Standard Oil Co Lubricant
US2331005A (en) * 1941-12-23 1943-10-05 Socony Vacuum Oil Co Inc Stabilized extreme pressure lubricant
US2516119A (en) * 1945-08-09 1950-07-25 Continental Oil Co Metal, phosphorus, and sulfur-containing organic compounds
US2607732A (en) * 1950-06-21 1952-08-19 Standard Oil Co Lubricants
US2607733A (en) * 1950-06-21 1952-08-19 Standard Oil Co Heavy duty lubricant
US2785130A (en) * 1953-12-21 1957-03-12 Texas Co Extreme pressure lubricant

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3029203A (en) * 1959-10-06 1962-04-10 Gulf Research Development Co Wire rope lubricant

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NL209632A (xx)
NL97640C (xx)
GB794688A (en) 1958-05-07
DE1020750B (de) 1957-12-12
FR1158801A (fr) 1958-06-19
BE550174A (xx)

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