EP1930400A1 - Schmierstoffzusammensetzung - Google Patents

Schmierstoffzusammensetzung Download PDF

Info

Publication number
EP1930400A1
EP1930400A1 EP06810740A EP06810740A EP1930400A1 EP 1930400 A1 EP1930400 A1 EP 1930400A1 EP 06810740 A EP06810740 A EP 06810740A EP 06810740 A EP06810740 A EP 06810740A EP 1930400 A1 EP1930400 A1 EP 1930400A1
Authority
EP
European Patent Office
Prior art keywords
composition
lubricating
molecular weight
acid
less
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP06810740A
Other languages
English (en)
French (fr)
Other versions
EP1930400B1 (de
EP1930400A4 (de
Inventor
Yukitoshi Fujinami
Hideto Kamimura
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Idemitsu Kosan Co Ltd
Original Assignee
Idemitsu Kosan Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Idemitsu Kosan Co Ltd filed Critical Idemitsu Kosan Co Ltd
Publication of EP1930400A1 publication Critical patent/EP1930400A1/de
Publication of EP1930400A4 publication Critical patent/EP1930400A4/de
Application granted granted Critical
Publication of EP1930400B1 publication Critical patent/EP1930400B1/de
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • 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
    • C10M141/00Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
    • C10M141/06Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic nitrogen-containing compound
    • 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
    • C10M169/00Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/06Mixtures of thickeners and 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
    • 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
    • C10M2203/1025Aliphatic fractions used as base material
    • 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
    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/028Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms
    • C10M2205/0285Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms used as base material
    • 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
    • C10M2207/02Hydroxy compounds
    • C10M2207/021Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/022Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least two hydroxy groups
    • 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
    • C10M2207/02Hydroxy 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
    • 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
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/106Carboxylix acids; Neutral salts thereof used as thickening agents
    • 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
    • C10M2207/10Carboxylix 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
    • C10M2207/128Carboxylix 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 containing hydroxy groups; Ethers thereof
    • C10M2207/1285Carboxylix 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 containing hydroxy groups; Ethers thereof used as thickening agents
    • 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
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/14Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/142Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings polycarboxylic
    • C10M2207/1426Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings polycarboxylic used as thickening agent
    • 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
    • C10M2207/287Partial esters
    • C10M2207/289Partial esters containing free hydroxy groups
    • 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
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/006Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions used as thickening agents
    • 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
    • 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
    • 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
    • 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
    • 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
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/10Amides of carbonic or haloformic acids
    • C10M2215/102Ureas; Semicarbazides; Allophanates
    • C10M2215/1026Ureas; Semicarbazides; Allophanates used as thickening material
    • 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
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/22Heterocyclic nitrogen compounds
    • C10M2215/223Five-membered rings containing nitrogen and carbon only
    • 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
    • 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
    • C10M2219/046Overbasedsulfonic acid salts
    • 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
    • C10M2229/00Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
    • C10M2229/04Siloxanes with specific structure
    • C10M2229/041Siloxanes with specific structure containing aliphatic substituents
    • 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
    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • 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
    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/01Physico-chemical properties
    • C10N2020/04Molecular weight; Molecular weight distribution
    • 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
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • 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
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/06Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
    • 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
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/08Resistance to extreme temperature
    • 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
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/10Inhibition of oxidation, e.g. anti-oxidants
    • 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
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/74Noack Volatility
    • 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
    • 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
    • C10N2040/02Bearings
    • 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
    • C10N2040/08Hydraulic fluids, e.g. brake-fluids
    • 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
    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/10Semi-solids; greasy

Definitions

  • the present invention relates to a lubricating composition and, more particularly, to a high temperature grease composition used for the lubrication of various machines and apparatuses such as automobiles, electric appliances, construction machines and machine tools as well as bearings and to a lubricating oil composition used for a long period of time under high temperatures in oil hydraulic, compression and vacuum pumps, bearings, gears, etc.
  • a lubricating composition is widely used in various machines such as automobiles, electric appliances, construction machines and machine tools. Such machines have been demanded year by year for meeting requirements of compact size, high output, light weight and simple maintenance. As a consequence, lubricating conditions of lubricating compositions become severe more and more.
  • To make a machine compact in size and high in output is to reduce the dimension thereof when the output thereof is the same. When the dimension is reduced, the heat energy discharged from surfaces of the machine is reduced to cause an increase of the temperature of a lubrication section thereof.
  • a material that has low heat conductivity such as a non-metal.
  • Simple maintenance has the same meaning as extension of service life.
  • the lubrication characteristics must be kept for a long time.
  • a lubricating composition having a long oxidation life so that the lubricating characteristics thereof can be maintained for a long period of time, particularly a high temperature grease composition having a high dropping point and a high temperature lubricating oil composition.
  • Patent Document 1 discloses a grease containing a metal deactivator for plastics and a lithium salt of a hydroxyfatty acid, a dilithium salt of an aliphatic dicarboxylic acid or a lithium salt of an aliphatic monocarboxylic acid.
  • Patent Document 2 discloses a grease composition including a base oil of a synthetic lube oil, a thickening agent of a urea compound, (a) an aromatic amine compound and (b) a hindered ester compound and further containing (c) at least one compound selected from phthalimide compounds and phosphoric ester compounds having an aromatic ring.
  • Patent Document 3 discloses a grease composition containing a base oil, a thickening agent, an antioxidant and an aromatic dibasic acid or a metal salt of an aromatic dibasic acid (excluding lithium terephthalate).
  • Patent Document 4 discloses a grease composition obtained by compounding a thickening agent composed of a C 12 to C 24 fatty acid having at least one hydroxyl group and a lithium salt of a C 2 to C 12 aliphatic dicarboxylic acid into a base oil which contains, as essential ingredients, a mineral oil having a kinematic viscosity at 40°C of 300 to 500 mm 2 /s and a synthetic hydrocarbon oil having a kinematic viscosity at 40°C of 20 to 300 mm 2 /s and which has a kinematic viscosity at 40°C of 60 to 200 mm 2 /s.
  • Patent Document 5 discloses a lubricating composition for rolling bearings which contains (a) a urethane prepolymer having an isocyanate group content of 6 to 10 % by weight, (b) a grease selected from a metal soap type grease and a non-metal soap type grease, and (c) an amine curing agent, and which has a hardness after curing of 60 to 85 in International Rubber Hardness Degree (IRHD).
  • IRHD International Rubber Hardness Degree
  • Patent Document 6 proposes the use of a styrenized diphenylamine, particularly 4,4'-bis( ⁇ -methylbenzyl)diphenylamine, as an antioxidant for a lubricating composition.
  • Patent Document 6 does not at all consider the conjoint use thereof with other antioxidants.
  • Patent Document 7 proposes an antiwear bearing oil composition in which an alkylated diphenylamine or a hindered phenol compound is incorporated as an antioxidant into a base oil together with a nonionic surfactant and an anti-wear agent for the purpose of improving anti-wearing property and stability against oxidation.
  • Patent Document 7 does not at all suggest the conjoint use of an amine-type antioxidant and a phenol compound for the purpose of improving the service life at high temperatures.
  • no sufficient studies have been made to develop an advantageous combination of an amine-type antioxidant with a phenol-type antioxidant in order to improve the effect of the prevention of deterioration by oxidation of the lubricating oil at high temperatures.
  • the present invention has been made for solving the above-mentioned problems and has as its object the provision of a lubricating composition, particularly a grease composition and a lubricating oil composition, which are hardly decomposed or volatilized even at high temperatures and have a long oxidation life so that the lubricating characteristics thereof can be maintained for a long period of time.
  • the present inventors have made an earnest study with a view toward accomplishing the above objects and have found that the objects can be fulfilled by compounding an aralkylated diphenylamine and a specific phenol compound into a base oil,
  • the present invention has been completed on the basis of such findings,
  • the present invention provides a lubricating composition containing a base oil, an aralkylated diphenylamine and a phenol compound having a molecular weight of not less than 340.
  • a base oil used in the lubricating composition of the present invention is not specifically limited. Any customarily employed mineral oil or synthetic oil may be used.
  • Examples of usable base oil include mineral oils such as paraffinic mineral oils, intermediate base mineral oils and naphthenic mineral oils; refined mineral oils obtained by processing the above mineral oils by solvent deasphalting, solvent extraction, hydrocracking, solvent dewaxing, hydrodewaxing or hydrorefining; mineral oils produced by isomerization of waxes; hydrocarbon synthetic oils such as poly- ⁇ -olefins; fats and oils; synthetic esters; and synthetic ethers.
  • base oils having a flash point of 180°C or higher, preferably 200°C or higher, are preferred.
  • a base oil having a flash point of 180°C or higher can be suitably used for a high temperature grease composition. It is also preferred that the base oil have a % C A of 1 or less, more preferably 0.5 or less.
  • C A represents an aromatic content as determined by the n-d-M ring analysis method (ASTM D 3238).
  • the term "% C A of a base oil” is intended to refer to C A of the base oil in terms of % by mass.
  • the base oil have a sulfur content of 20 ppm or less, more preferably 10 ppm or less.
  • the poly- ⁇ -olefin used as the base oil in the present invention there may be used various kinds of ⁇ -olefin polymers. Generally used are polymers of a C 6 to C 18 ⁇ -olefin having a lubrication viscosity. From the standpoint of thermal stability, sealing property and lubricity, polymers of 1-dodecene, 1-dacene or 1-octene are preferred. For reasons of thermal stability, hydrogen-treated poly- ⁇ -olefins are particularly suitably used. These poly- ⁇ -olefns may be used singly or as a mixture of two or more thereof.
  • the kinematic viscosity of the base oil is not specifically restricted.
  • the kinematic viscosity of the base oil is generally suitably selected from a range of 2 mm 2 /s to 600 mm 2 /s at 40°C, more preferably 10 mm 2 /s to 400 mm 2 /s.
  • R 1 and R 4 each independently preferably represent a C 0 to C 24 alkyl group
  • R 2 and R 3 each independently preferably represent a C 1 to C 5 alkylene group, more preferably a C 1 to C 3 alkylene group.
  • C 0 means that the corresponding substituent R 1 or R 4 is not present.
  • Specific examples of the aralkylated diphenylamine include 4,4'-bis( ⁇ , ⁇ -dimethylbenzyl)diphenylamine, 4,4'-bisbenzyldiphenylamine, 4,4'-diphenethyldiphenylamine and 4,4'-bis( ⁇ -methylbenzyl)diphenylamine.
  • the aralkylated diphenylamine is preferably used in an amount of 0.01 to 10 % by mass, more preferably 0.1 to 5 % by mass, particularly preferably 0.1 to 2 % by mass, based on the lubricating composition.
  • the amount is 0.01 % by mass or greater, deterioration by oxidation can be effectively prevented.
  • An amount of 10 % by mass or less is economically advantageous.
  • One preferred example of the phenol compound having a molecular weight of not less than 340, preferably not less than 350, used in the present invention is a compound represented by the following chemical formula (2).
  • R 5 is preferably a C 1 to C 18 alkyl group
  • R 6 is preferably a C 1 to C 5 alkylene group, particularly preferably C 1 to C3 alkylene group
  • R 7 is preferably a C 1 to C 24 alkyl group
  • n is 1 or 2.
  • octadecyl-3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate molecular weight: 520.89.
  • the phenol compound having a molecular weight of not less than 340 used in the present invention there may be mentioned a bisphenol compound.
  • the bisphenol compound include 2,2'-methylenebis(4-methyl-6-tert-butylphenol) (molecular weight: 340.51).
  • the phenol compound having a molecular weight of not less than 340 used in the present invention there may be mentioned a polyphenol compound other than the bisphenol compound.
  • the polyphenol compound include 1,1,3-tris(2-methyl-4-hydroxy-5-tert-butylphenyl)butane (molecular weight: 544.83), 1,3,5-trimethyl-2,4,6-tris(3,5-di-tert-butyl-4-hydroxybenzyl)benzene (molecular weight: 775.21), tetrakis-[methylene-3-(3',5'-di-tert-butyl-4'-hydroxyphenyl)propionate]methene (molecular weight: 1177.66), bis[3,3'-bis-(4'-hydroxy-3'-tert-butylphenyl)butyric acid] glycol ester (molecular weight: 794.42), 1,3,5-tris(3',5'-di-tert)
  • the phenol compound having a molecular weight of not less than 340 used in the present invention there may be mentioned a tocophenol (molecular weight 430.71) and its derivatives.
  • a tocophenol molecular weight 430.71
  • the effect of the prevention of deterioration by oxidation is significant
  • Such an effect is further improved when the molecular weight is not less than 350.
  • the molecular weight is not greater than 1,500, there is no fear of causing dissolution failure in the base oil.
  • phenol compounds having a molecular weight of not less than 340 octadecyl-3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate (molecular weight: 520.89) and 2,2'-methylenebis(4-ethyl-6-tert-butylphenol) (molecular weight: 368.54) are particularly preferred from the view point of improving the effect of the prevention of deterioration by oxidation.
  • the phenol compound having a molecular weight of not less than 340 is preferably used in an amount of 0.01 to 10 % by mass, more preferably 0.1 to 5 % by mass, particularly preferably 0.1 to 3 % by mass, based on the lubricating composition, When the amount is 0.01 % by mass or more, the effect of the prevention of deterioration by oxidation is obtainable. An amount of 10 % by mass or less is advantageous from the standpoint of economy.
  • the thickening agent used in the present invention is not specifically restricted.
  • a soap thickening agent or a non-soap thickening agent may be used.
  • Preferably used is a thickening agent which can provide a grease composition having a dropping point of 230°C or higher.
  • a possibility of causing problems in relation to lubrication such as softening at high temperatures and resulting leakage or baking can be suppressed.
  • the soap thickening agent there may be mentioned a metal soap obtained by saponifying a carboxylic acid or its ester with a metal hydroxide such as an alkali metal hydroxide or an alkaline earth metal hydroxide.
  • Examples of the metal include sodium, calcium, lithium and aluminum.
  • Examples of the carboxylic acid include fats and oils, crude fatty acids obtained by hydrolyzing fats and oils and removing glycerin therefrom, monocarboxylic acids such as stearic acid, monohydroxycarboxylic acids such as 12-hydroxystearic acid, dibasic carboxylic acids such as azelaic acid, and aromatic carboxylic acids such as terephthalic acid, salicylic acid and benzoic acid.
  • These soap thickening agents may be used singly or in combination.
  • a preferred example of the soap thickening agent is a lithium soap using 12-hydroxystearic acid.
  • the soap thickening agent As another type of the soap thickening agent, there may be mentioned various complex soaps.
  • the complex soap include a lithium complex soap, an aluminum complex soap and a calcium complex soap.
  • the lithium complex soap may be obtained by reacting a fatty acid, such as stearic acid, oleic acid or palmitic acid, and/or a C 12 to C 24 hydroxyfatty acid having at least one hydroxyl group with a lithium compound, such as lithium hydroxide, together with an aromatic carboxylic acid and/or C 2 to C 12 (more preferably C 4 to C 9 ) aliphatic dicarboxylic acid.
  • a lithium complex soap is a more preferable thickening agent because of its superior heat resistance as compared with a lithium soap.
  • C 12 to C 24 hydroxyfatty acid 12-hydroxystearic acid is most preferred, though any other hydroxyfatty acid may be used.
  • Such other hydroxyfatty acids may be, for example, 12-hydroxylauric acid and 16-hydroxypalmitic acid.
  • aromatic carboxylic acid there may be mentioned benzoic acid, o-phthalic acid, m-phthalic acid, terephthalic acid, trimellitic acid, pyromellitic acid, salicylic acid and p-hydroxybenzoic acid.
  • azelaic acid is most preferred, though any other aliphatic dicarboxylic acid may be used.
  • Such other aliphatic dicarboxylic acid may be, for example, sebacic acid, oxalic acid, malonic acid, succinic acid, adipic acid, pimelic acid, suberic acid, undecanedicarboxylic acid and dodecanedicarboxylic acid. It is preferred that the aromatic carboxylic acid and/or C 2 to C 12 aliphatic dicarboxylic acid be present in an amount of 20 to 90 % by mass based on a total mass of the fatty acid and/or C 12 to C 24 hydroxyfatty acid having at least one hydroxyl group and the aromatic carboxylic acid and/or C 2 to C 12 aliphatic dicarboxylic acid. This is because a thickening agent having good thermal stability may be obtained and a grease composition having a long service life at high temperatures may be advantageously obtainable when the amount is within the range of 20 to 90 % by mass.
  • a urea compound or bentonite treated with an organic compound may be used.
  • the urea compound used as the thickening agent there may be mentioned a diurea compound, a triurea compound, a tetraurea compound and a urea-urethane compound. Because the urea compound has excellent heat resistance and water resistance and is particularly excellent in stability at high temperatures, it is suitably used in a high temperature environment.
  • the diurea compound there may be mentioned, for example, a compound represented by the formula R 8 NHCONHR 9 NHCONHR 8 (wherein R 8 represents a straight chained or branched, saturated or unsaturated C 6 to C 24 alkyl group and R 9 represents a divalent C 6 to C 15 aromatic hydrocarbon group).
  • the typical diurea compound may be obtained by reaction of a diisocyanate with a monoamine.
  • the diisocyanate may be, for example, diphenylmethane diiocyanate, phenylene diisocyanate, diphenyl diisocyanate, phenyl diisocyanate or tolylene diisocyanate.
  • the monoamine may be, for example, octylamine, dodecylamine, hexadecylamine, cyclohexylamine, aniline, toluidine, octadecylamine or oleylamine.
  • Conventionally known urea thickening agents may also be suitably used.
  • various complex soaps and urea compounds are preferred.
  • the complex soaps and urea compounds may be used singly or in combination of two or more thereof.
  • the compounding amount of the thickening agent in the grease composition is not specifically restricted as long as the intended grease characteristics may be obtained but is preferably 10 to 30 % by mass, more preferably 10 to 20 % by mass, based on the grease composition.
  • the thickening agent used in the grease composition of the present invention serves to impart a desired consistency thereto. When the amount of the thickening agent is excessively small, a desired consistency is not obtainable. When the compounding amount is excessively large, the lubricity of the grease is reduced.
  • the grease composition of the present invention contain a base oil having a flash point of 180°C or higher, an aralkylated diphenylamine, a phenol compound having a molecular weight of not less than 340 and, additionally, a thickening agent for reasons of maintaining the lubricating characteristics at high temperatures for a long period of time.
  • the grease composition and lubricating oil composition according to the present invention may optionally contain an additive or additives such as an anti-corrosive agent, an extreme pressure agent, a metal deactivator, a metallic detergent, a non-metallic detergent, an antifoaming agent, a viscosity increasing agent, a colorant and a water repellent agent.
  • an additive or additives such as an anti-corrosive agent, an extreme pressure agent, a metal deactivator, a metallic detergent, a non-metallic detergent, an antifoaming agent, a viscosity increasing agent, a colorant and a water repellent agent.
  • an additive or additives such as an anti-corrosive agent, an extreme pressure agent, a metal deactivator, a metallic detergent, a non-metallic detergent, an antifoaming agent, a viscosity increasing agent, a colorant and a water repellent agent.
  • the anti-corrosive agent there may be mentioned a metallic sulfonate and
  • a lubricating composition particularly a grease composition and a lubricating oil composition, which are hardly decomposed or volatilized even at high temperatures and which have a long oxidation life so that the lubricating characteristics thereof can be maintained for a long period of time.
  • 1-decene oligomer (kinematic viscosity (40°C): 30 mm 2 /s) was used.
  • the base oil was compounded with an antioxidant, a metal deactivator, an anti-corrosive agent and an antifoaming agent to obtain four kinds of lubricating oil compositions.
  • Each of the four lubricating oil compositions was measured for the above-described oil remaining percent (6) and fluidity (7). The results are summarized in Table 2.
  • the lubricating oil composition of the present invention has a high oil remaining percent and fluidity and, therefore, is hardly decomposed or volatilized even at high temperatures and has a long oxidation life.
  • the lubricating composition of the present invention which has long oxidation life and can maintain its lubricating characteristics for a long time even when exposed to high temperatures, is suitably used, as a high temperature lubricating composition, particularly as a high temperature grease composition and as a high temperature lubricating oil composition, for lubrication of various machines and apparatuses such as automobiles, electric appliances, construction machines and machine tools as well as bearings.
  • the lubricating composition is suitably used for lubrication in internal combustion engines, torque converters, fluid couplings, radial bearings, rolling bearings, oil retaining bearings, fluid bearings, compressors, chain drives, gears, oil hydraulic circuits, vacuum pumps, clock parts, hard disk apparatuses, refrigerators, cutting, rolling, metal drawing, form rolling, forging, heat treatment, heat media, washing, shock absorbers, corrosion prevention, brake members and sealing devices.
EP06810740A 2005-09-29 2006-09-28 Schmierstoffzusammensetzung Active EP1930400B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2005284217 2005-09-29
PCT/JP2006/319293 WO2007037322A1 (ja) 2005-09-29 2006-09-28 潤滑組成物

Publications (3)

Publication Number Publication Date
EP1930400A1 true EP1930400A1 (de) 2008-06-11
EP1930400A4 EP1930400A4 (de) 2009-02-18
EP1930400B1 EP1930400B1 (de) 2011-08-03

Family

ID=37899746

Family Applications (1)

Application Number Title Priority Date Filing Date
EP06810740A Active EP1930400B1 (de) 2005-09-29 2006-09-28 Schmierstoffzusammensetzung

Country Status (5)

Country Link
US (1) US20090170738A1 (de)
EP (1) EP1930400B1 (de)
JP (1) JP5249584B2 (de)
CN (1) CN101278036B (de)
WO (1) WO2007037322A1 (de)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013017528A1 (en) * 2011-07-29 2013-02-07 Shell Internationale Research Maatschappij B.V. Grease composition

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5505923B2 (ja) * 2009-02-02 2014-05-28 協同油脂株式会社 潤滑油組成物及びグリース
CN103254966B (zh) * 2012-02-21 2015-05-20 中国石油化工股份有限公司 一种复合钙基四聚脲润滑脂及其制备方法
CN103254969B (zh) * 2012-02-21 2015-05-20 中国石油化工股份有限公司 一种复合钙基四聚脲润滑脂及其制备方法
CN103254968B (zh) * 2012-02-21 2015-03-18 中国石油化工股份有限公司 一种复合钙基四聚脲润滑脂及其制备方法
CN103289783B (zh) * 2012-02-22 2015-05-20 中国石油化工股份有限公司 一种复合钙基八聚脲润滑脂及其制备方法
CN103289784B (zh) * 2012-02-22 2015-05-20 中国石油化工股份有限公司 一种复合钙基六聚脲润滑脂及其制备方法
CN103289786B (zh) * 2012-02-22 2015-05-20 中国石油化工股份有限公司 一种复合钙基八聚脲润滑脂及其制备方法
JP5988376B2 (ja) * 2012-12-03 2016-09-07 協同油脂株式会社 鉄道車両の主電動機軸受用グリース組成物及び軸受
JP6744708B2 (ja) * 2015-01-21 2020-08-19 セイコーインスツル株式会社 転がり軸受用グリース、転がり軸受、転がり軸受装置及び情報記録再生装置
CN105802716B (zh) * 2015-01-21 2020-03-24 精工电子有限公司 滚动轴承用润滑脂、滚动轴承、滚动轴承装置以及信息记录重放装置
CN106753694A (zh) * 2016-11-23 2017-05-31 江苏金戈光电玻璃技术有限公司 一种电机润滑油添加剂
CN106635368A (zh) * 2016-12-16 2017-05-10 东莞市粤钢不锈钢制品有限公司 拉丝环保润滑剂及其制备、使用方法
CN108130179A (zh) * 2017-12-18 2018-06-08 上海摩克润滑油技术有限公司 一种汽车液压制动系统润滑脂
CN109667835B (zh) * 2019-01-25 2020-09-01 中国科学院兰州化学物理研究所 含浸凝胶润滑剂的自润滑含油轴承及其制备方法
EP3757195A1 (de) 2019-06-27 2020-12-30 TE Connectivity Germany GmbH Ausgabefähige fettdichtmittel, verfahren zur herstellung davon, crimpverbindung, verfahren zur herstellung davon und verwendung der ausgabefähigen fettdichtmittel

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3944492A (en) * 1966-04-07 1976-03-16 Uniroyal, Inc. Lubricant compositions containing N-substituted naphthylamines as antioxidants
US5840672A (en) * 1997-07-17 1998-11-24 Ethyl Corporation Antioxidant system for lubrication base oils
EP0994175A2 (de) * 1998-10-16 2000-04-19 Ethyl Corporation Turbineölenmit ausgezeigneter Oxidationsstabilität bei hoher Temperatur
WO2004074412A2 (en) * 2003-02-18 2004-09-02 Shell Internationale Research Maatschappij B.V. Lubricating oil compositions
EP1529830A1 (de) * 2003-11-04 2005-05-11 Chevron Oronite S.A. Aschefreie Zusatzformulierungen für Hydrauliköl

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3505225A (en) * 1966-04-07 1970-04-07 Uniroyal Inc Derivatives of diphenylamine and the phenylnaphthylamines as antioxidants and as synergists with dialkyl 3,3'-thiodipropionates
JP2954744B2 (ja) * 1990-10-04 1999-09-27 東燃株式会社 潤滑油組成物
JP2922666B2 (ja) * 1991-03-19 1999-07-26 三菱石油株式会社 高粘度耐熱潤滑油組成物
JPH0641572A (ja) * 1992-05-29 1994-02-15 Tonen Corp 潤滑油組成物
JPH0953087A (ja) * 1995-08-11 1997-02-25 Seiko Kagaku Kk 潤滑剤酸化防止剤及び潤滑剤組成物
US6239085B1 (en) * 1998-10-23 2001-05-29 Exxon Research And Engineering Company Grease composition containing pao, alkylaromatic synthetic fluid and white oil for industrial bearings
US6232278B1 (en) * 1998-12-22 2001-05-15 Kyodo Yushi Co., Ltd. Lubricating grease composition
JP2001003074A (ja) * 1999-06-18 2001-01-09 Seiko Instruments Inc ころがり軸受封入用グリース
JP4309635B2 (ja) * 2001-10-12 2009-08-05 新日本石油株式会社 内燃機関用潤滑油組成物
JP2005008744A (ja) * 2003-06-18 2005-01-13 Showa Shell Sekiyu Kk グリース組成物
JP4507158B2 (ja) * 2003-07-25 2010-07-21 財団法人石油産業活性化センター 環境適合性および省燃費性に優れたガソリンエンジン油組成物

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3944492A (en) * 1966-04-07 1976-03-16 Uniroyal, Inc. Lubricant compositions containing N-substituted naphthylamines as antioxidants
US5840672A (en) * 1997-07-17 1998-11-24 Ethyl Corporation Antioxidant system for lubrication base oils
EP0994175A2 (de) * 1998-10-16 2000-04-19 Ethyl Corporation Turbineölenmit ausgezeigneter Oxidationsstabilität bei hoher Temperatur
WO2004074412A2 (en) * 2003-02-18 2004-09-02 Shell Internationale Research Maatschappij B.V. Lubricating oil compositions
EP1529830A1 (de) * 2003-11-04 2005-05-11 Chevron Oronite S.A. Aschefreie Zusatzformulierungen für Hydrauliköl

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Week 199718 Thomson Scientific, London, GB; AN 1997-197418 XP002504339 & JP 09 053087 A (SEIKO KAGAKU KK) 25 February 1997 (1997-02-25) *
DATABASE WPI Week 200124 Thomson Scientific, London, GB; AN 2001-229188 XP002504321 & JP 2001 003074 A (SEIKO INSTR INC) 9 January 2001 (2001-01-09) *
See also references of WO2007037322A1 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013017528A1 (en) * 2011-07-29 2013-02-07 Shell Internationale Research Maatschappij B.V. Grease composition

Also Published As

Publication number Publication date
CN101278036A (zh) 2008-10-01
US20090170738A1 (en) 2009-07-02
EP1930400B1 (de) 2011-08-03
JP5249584B2 (ja) 2013-07-31
CN101278036B (zh) 2011-04-20
JPWO2007037322A1 (ja) 2009-04-09
WO2007037322A1 (ja) 2007-04-05
EP1930400A4 (de) 2009-02-18

Similar Documents

Publication Publication Date Title
EP1930400B1 (de) Schmierstoffzusammensetzung
EP2785821B1 (de) Schmierfettzusammensetzung
EP2264132B1 (de) Schmierfettzusammensetzung und lager
EP2687584B1 (de) Schmierfettzusammensetzung
US20120314985A1 (en) Grease composition for hub unit bearing employing an angular contact ball bearing and hub unit bearing
JP5738712B2 (ja) グリース組成物
JP3370829B2 (ja) 潤滑グリース組成物
JP2008239706A (ja) グリース組成物及び軸受
WO2012115141A1 (ja) グリース組成物
EP2631284B1 (de) Schmierfettzusammensetzung
JP2006316081A (ja) グリース組成物およびグリース封入転がり軸受
JP6845633B2 (ja) グリース組成物
US20140336090A1 (en) Grease composition and bearing
EP3178910B1 (de) Schmierfettzusammensetzung
JPH08188790A (ja) 潤滑油組成物及びグリース組成物
WO2013017528A1 (en) Grease composition
JP2005132900A (ja) グリース組成物及び転がり軸受
JPH11343492A (ja) 潤滑剤組成物
WO2023182533A1 (ja) グリース組成物
WO2023182532A1 (ja) グリース組成物
JP2007217521A (ja) グリース組成物および該グリース封入軸受
JP2019163409A (ja) グリース組成物及び転がり軸受
JP2003201494A (ja) 潤滑剤組成物
JP2016020481A (ja) グリース組成物

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20080328

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): DE FR

RBV Designated contracting states (corrected)

Designated state(s): DE FR

A4 Supplementary search report drawn up and despatched

Effective date: 20090119

17Q First examination report despatched

Effective date: 20090420

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

DAX Request for extension of the european patent (deleted)
RIC1 Information provided on ipc code assigned before grant

Ipc: C10M 169/06 20060101ALI20110204BHEP

Ipc: C10M 141/06 20060101AFI20110204BHEP

Ipc: C10M 117/00 20060101ALI20110204BHEP

Ipc: C10M 115/08 20060101ALI20110204BHEP

Ipc: C10N 40/08 20060101ALI20110204BHEP

Ipc: C10N 40/02 20060101ALI20110204BHEP

Ipc: C10N 50/10 20060101ALI20110204BHEP

Ipc: C10N 30/10 20060101ALI20110204BHEP

Ipc: C10N 30/08 20060101ALI20110204BHEP

Ipc: C10N 20/04 20060101ALI20110204BHEP

Ipc: C10N 20/00 20060101ALI20110204BHEP

Ipc: C10M 133/12 20060101ALI20110204BHEP

Ipc: C10N 30/06 20060101ALI20110204BHEP

Ipc: C10M 129/14 20060101ALI20110204BHEP

Ipc: C10M 129/76 20060101ALI20110204BHEP

Ipc: C10M 129/10 20060101ALI20110204BHEP

Ipc: C10N 40/00 20060101ALI20110204BHEP

Ipc: C10N 40/04 20060101ALI20110204BHEP

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): DE FR

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602006023551

Country of ref document: DE

Effective date: 20110929

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed

Effective date: 20120504

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602006023551

Country of ref document: DE

Effective date: 20120504

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 11

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DK

Payment date: 20170626

Year of fee payment: 7

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20180930

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20230802

Year of fee payment: 18