EP3425032B1 - Lubricating oil composition - Google Patents

Lubricating oil composition Download PDF

Info

Publication number
EP3425032B1
EP3425032B1 EP17760169.7A EP17760169A EP3425032B1 EP 3425032 B1 EP3425032 B1 EP 3425032B1 EP 17760169 A EP17760169 A EP 17760169A EP 3425032 B1 EP3425032 B1 EP 3425032B1
Authority
EP
European Patent Office
Prior art keywords
lubricating oil
alkaline earth
earth metal
oil composition
mass
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.)
Active
Application number
EP17760169.7A
Other languages
German (de)
English (en)
French (fr)
Other versions
EP3425032A1 (en
EP3425032A4 (en
Inventor
Masato YOKOMIZO
Hideki Kamano
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 EP3425032A1 publication Critical patent/EP3425032A1/en
Publication of EP3425032A4 publication Critical patent/EP3425032A4/en
Application granted granted Critical
Publication of EP3425032B1 publication Critical patent/EP3425032B1/en
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
    • C10M167/00Lubricating compositions characterised by the additive being a mixture of a macromolecular compound, a non-macromolecular compound and a compound of unknown or incompletely defined constitution, each of these compounds being essential
    • 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
    • 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
    • C10M2205/022Ethene
    • 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
    • C10M2205/026Butene
    • 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
    • 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
    • C10M2207/028Overbased salts thereof
    • 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
    • C10M2207/26Overbased carboxylic acid salts
    • C10M2207/262Overbased carboxylic acid salts derived from hydroxy substituted aromatic acids, e.g. salicylates
    • 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
    • C10M2215/02Amines, 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
    • 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
    • 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
    • C10M2223/045Metal containing thio derivatives
    • 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
    • C10N2010/04Groups 2 or 12
    • 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
    • C10N2030/02Pour-point; Viscosity index
    • 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
    • C10N2030/04Detergent property or dispersant property
    • 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
    • C10N2030/40Low content or no content compositions
    • C10N2030/42Phosphor free or low phosphor content 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
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/40Low content or no content compositions
    • C10N2030/43Sulfur free or low sulfur content 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
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/52Base number [TBN]
    • 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
    • C10N2030/68Shear stability
    • 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
    • C10N2040/044Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for manual transmissions

Definitions

  • the present invention relates to a lubricating oil composition.
  • the present invention relates to a lubricating oil composition, and, for example, relates to a lubricating oil composition favorably used for transmissions.
  • viscosity reduction is promoted for reducing resistance to stirring.
  • viscosity reduction in lubricating oil may lower oil film strength in a high-temperature region, and there will be fears of reduction in seizure resistance, anti-wear performance and fatigue resistance.
  • it is effective to keep a high viscosity of lubricating oil in a high-temperature region and to lower the viscosity thereof in a normal-temperature region.
  • it is effective to increase the viscosity index of lubricating oil.
  • a viscosity index improver such as polymer will have to be added to lubricating oil.
  • the polymer receives shear in use to reduce the viscosity of lubricating oil. Consequently, in the case where a viscosity index improver is blended in lubricating oil, the viscosity lowering in actual vehicle driving will have to be taken into consideration.
  • Down-sizing and weight-saving is under way in planning transmissions. Owing to down-sizing and weight-saving of transmissions, the mechanical load to a lubrication part increases, and therefore further improved lubrication performance is desired for the lubricating oil to be loaded. In addition, thermal load also increases, and therefore further more improved heat resistance and oxidation stability is desired for lubricating oil.
  • sludge When heat resistance and oxidation stability of lubricating oil worsens, sludge may form, and when adhering to lubrication sites, it may cause lubrication failure. For example, sludge adhesion may cause operation failure of bearings, etc.
  • sludge adhesion in the synchromesh mechanism that takes care of variable speed level change may cause reduction in shift feeling owing to reduction in friction performance and may further cause driving failure owing to synchronizer ring immobilization.
  • a viscosity index improver excellent in shear stability is blended in a low-viscosity base oil to further lower the viscosity of lubricating oil (kinematic viscosity at 100°C: at least 6.2 mm 2 /s).
  • a viscosity index improver excellent in shear stability is blended in a low-viscosity base oil to further lower the viscosity of lubricating oil (kinematic viscosity at 100°C: at least 6.2 mm 2 /s).
  • viscosity reduction of lubricating oil is tried, not adding a polymethacrylate compound thereto (kinematic viscosity at 100°C: about 6.0 mm 2 /s or more in Examples), and with that, a molybdenum compound is blended in the lubricating oil to prevent synchromesh abrasion to thereby maintain friction characteristics.
  • EP 0 341 574 A1 is concerned with a lubricating oil composition which is low in fatigue failure of a metal under repeated high contact stress, and also high in a traction coefficient, and yet excellent in oxidation resistance.
  • an object of the present invention is to provide a lubricating oil composition capable of attaining viscosity reduction and preventing viscosity lowering in actual vehicle driving, and capable of improving heat resistance and oxidation resistance.
  • a lubricating oil composition containing, along with a base oil, specific components (A) to (C) as indispensable components can solve the above-mentioned problems.
  • the present invention provides the following [1] to [5]:
  • a lubricating oil composition capable of attaining viscosity reduction and preventing viscosity lowering in actual vehicle driving, and capable of improving heat resistance and oxidation resistance.
  • the "kinematic viscosity at 100°C” and the “kinematic viscosity at 40°C” of the base oil or the lubricating oil composition mean values measured according to the method described in JIS K2283:2000.
  • the content of the alkaline earth metal atom in the lubricating oil composition means a value measured according to JPI-5S-38-92.
  • the "alkaline earth metal atom” indicates a beryllium atom, a magnesium atom, a calcium atom, a strontium atom, and a barium atom.
  • the lubricating oil composition of this embodiment contains, along with a base oil, (A) an olefin oligomer having a mass average molecular weight of 500 or more and 5,000 or less, (B) an antioxidant containing (B-1) a phenol-based antioxidant and (B-2) an amine-based antioxidant, and (C) an alkaline earth metal-based detergent, wherein the content of the alkaline earth metal-based detergent (C) is 1,700 ppm by mass or more and 2,700 ppm by mass or less in terms of an alkaline earth metal atom thereof based on the total amount of the lubricating oil composition, and the kinematic viscosity at 100°C of the lubricating oil composition is 4.0 mm 2 /s or more and 6.0 mm 2 /s or less.
  • the total content of the base oil, the olefin oligomer (A), the antioxidant (B) and the alkaline earth metal-based detergent (C) is, based on the total amount of the lubricating oil composition (100% by mass), preferably 70% by mass or more, more preferably 75% by mass or more, even more preferably 80% by mass or more, further more preferably 85% by mass or more, and still further more preferably 90% by mass or more, and is generally 100% by mass or less, preferably 99.9% by mass or less, more preferably 99% by mass or less.
  • the lubricating oil composition of this embodiment contains an olefin oligomer (A), and the mass average molecular weight of the olefin oligomer (A) is needed to be 500 or more and 5,000 or less.
  • the olefin oligomer (A) has fluidity in a high-temperature region of a device, for example, a transmission, and has an effect of washing out formed sludge.
  • a device for example, a transmission
  • the olefin oligomer (A) has fluidity in a high-temperature region of a device, for example, a transmission, and has an effect of washing out formed sludge.
  • the molecular weight thereof is less than 500, the olefin oligomer evaporates in a high-temperature region and could not sufficient exhibit the washing effect.
  • the molecular weight thereof is more than 5,000, the olefin oligomer (A) could not keep fluidity in a high-temperature region and could not sufficiently exhibit the effect of washing out sludge.
  • the mass average molecular weight of the olefin oligomer (A) is preferably 600 or more and 4,500 or less, more preferably 700 or more and 4,000 or less, even more preferably 800 or more and 3,000 or less.
  • the olefin oligomer (A) may be any one having a polyolefin skeleton and having a molecular weight of 500 or more and 5,000 or less.
  • the olefin oligomer (A) preferably contains a structural unit derived from an unsaturated hydrocarbon monomer having 2 or more and 5 or less carbon atoms, and examples thereof include an olefin oligomer such as a propylene oligomer, an isobutylene oligomer, a polybutene, a polyisobutylene, an octene oligomer, a decene oligomer, and an ethylene-propylene oligomer. Above all, a polybutene-1 is preferably used.
  • One kind of the olefin oligomer (A) may be used alone or two or more kinds thereof may be used in combination.
  • the olefin oligomer (A) is blended such that the kinematic viscosity at 100°C of the lubricating oil composition of this embodiment falls within a range of 4.0 mm 2 /s or more and 6.0 mm 2 /s or less.
  • the content of the olefin oligomer (A) having a mass average molecular weight of 500 or more and 5,000 or less in the lubricating oil composition of this embodiment is, based on the total amount of the lubricating oil composition, preferably 0.8% by mass or more and 4.5% by mass or less, more preferably 1% by mass or more and 4% by mass or less, even more preferably 1.2% by mass or more and 2.5% by mass or less.
  • the lubricating oil composition of this embodiment contains an antioxidant (B), and the antioxidant (B) contains a phenol-based antioxidant (B-1) and an amine-based antioxidant (B-2).
  • the antioxidant (B) is needed to contain both the phenol-based antioxidant (B-1) and the amine-based antioxidant (B-2), and the use of either one alone fails to attain a sufficient antioxidation performance.
  • the phenol-based antioxidant (B-1) may be any compound having a phenol structure and having an effect of preventing oxidation of the lubricating oil composition.
  • phenol-based antioxidant (B-1) examples include 2,6-di-tert-butyl-4-methylphenol, 2,6-di-tert-butyl-4-ethylphenol, 2,4,6-tri-tert-butylphenol, 2,6-di-tert-butyl-4-hydroxymethylphenol, 2,6-di-tert-butylphenol, 2,4-dimethyl-6-tert-butylphenol, 2,6-di-tert-butyl-4-(N,N'-dimethylaminomethyl)phenol, 2,6-di-tert-amyl-4-methylphenol, 2,6-di-tert-amyl-p-cresol, 4,4'-methylenebis(2,6-di-tert-butylphenol), 4,4'-bis(2,6-di-tert-butylphenol), 4,4'-bis(2-methyl-6-tert-butylphenol), 2,2'-methylenebis(4-ethyl-6-tert
  • one kind of the phenol-based antioxidant (B-1) may be used alone or two or more kinds thereof may be used in combination.
  • the amine-based antioxidant (B-2) usable in this embodiment is not specifically limited. Examples thereof include compounds represented by the following general formula (B-2-1). Ar 1 -NH-Ar 2 (B-2-1)
  • Ar 1 and Ar 2 each independently represent an aryl group having 6 to 24 carbon atoms selected from a phenyl group, a phenyl group substituted with an alkyl group, a phenyl group substituted with an aralkyl group, a naphthyl group, and a naphthyl group substituted with an alkyl group.
  • the amine-based antioxidant (B-2) is preferably selected from phenyl- ⁇ -naphthylamines represented by the following general formula (B-2-2) and diphenylamines represented by the following general formula (B-2-3).
  • R 1 represents a hydrogen atom, or an alkyl group having 1 to 18 carbon atoms.
  • R 2 and R 8 each independently represent a hydrogen atom, an alkyl group having 1 to 18 carbon atoms, or an aralkyl group having 7 to 18 carbon atoms.
  • amine-based antioxidant (B-2) examples include monoalkyldiphenylamines such as monooctyldiphenylamine, and monononyldiphenylamine; dialkyldiphenylamines such as 4,4'-dibutyldiphenylamine, 4,4'-dipentyldiphenylamine, 4,4'-dihexyldiphenylamine, 4,4'-diheptyldiphenylamine, 4,4'-dioctyldiphenylamine, and 4,4'-dinonyldiphenylamine; polyalkyldiphenylamines such as tetrabutyldiphenylamine, tetrahexyldiphenylamine, tetraoctyldiphenylamine, and tetranonyldiphenylamine; naphthylamines such as ⁇ -naphthylamine, and phenyl- ⁇ -naph
  • one kind of the amine-based antioxidant (B-2) may be used alone or two or more kinds thereof may be used in combination.
  • phenol-based antioxidant (B-1) and the amine-based antioxidant (B-2) to be used in combination for the antioxidant (B) include arbitrary combinations of pentaerythritol tetrakis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate] or octadecyl-3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate (B-1), and monobutylphenylmonooctylphenylamine or N-p-t-octylphenyl-1-naphthylamine (B-2).
  • the content of the antioxidant (B) containing the phenol-based antioxidant (B-1) and the amine-based antioxidant (B-2) is, based on the total amount of the lubricating oil composition, preferably 0.5% by mass or more and 3.0% by mass or less, more preferably 0.5% by mass or more and 2.0% by mass or less, even more preferably 1% by mass or more and 2% by mass or less.
  • the content of the antioxidant (B) means the total amount of the phenol-based antioxidant (B-1) and the amine-based antioxidant (B-2).
  • the content of the antioxidant (B) is 0.5% by mass or more, the antioxidation effect can be sufficiently exhibited.
  • the upper limit of the content of the antioxidant (B) may be well 3.0% by mass.
  • the ratio by mass of the amine-based antioxidant (B-2) to the phenol-based antioxidant (B-1) [(B-2)/(B-1)] is preferably 1/3 to 3/1 or so, more preferably 1/2 to 2/1 or so.
  • the total content of the phenol-based antioxidant (B-1) and the amine-based antioxidant (B-2) in the antioxidant (B) is, based on the total amount of the antioxidant (B), preferably 60% by mass or more and 100% by mass or less, more preferably 70% by mass or more and 100% by mass or less, even more preferably 80% by mass or more and 100% by mass or less, further more preferably 90% by mass or more and 100% by mass or less, still further more preferably 99% by mass or more and 100% by mass or less.
  • the antioxidant (B) is indispensable, but does not exclude containing any other antioxidant within a range not detracting from the advantageous effects of the present invention.
  • the other antioxidant include a molybdenum amine complex-based antioxidant.
  • the molybdenum amine complex-based antioxidant includes hexavalent molybdenum compounds, specifically those produced by reacting molybdenum trioxide and/or molybdic acid and an amine compound, for example, the compounds obtained according to the production method described in JP 2003-252887 A .
  • the lubricating oil composition of this embodiment contains an alkaline earth metal-based detergent (C), and the content of the alkaline earth metal-based detergent (C) is 1,700 ppm by mass or more and 2,700 ppm by mass or less in terms of an alkaline earth metal atom thereof based on the total amount of the lubricating oil composition.
  • C alkaline earth metal-based detergent
  • the alkaline earth metal-based detergent (C) prevents sludge formation owing to the acid neutralization effect for the degraded components formed in oil, and has a detergent effect for sludge dispersion.
  • the content of the alkaline earth metal-based detergent (C) is less than 1,700 ppm by mass in terms of an alkaline earth metal atom thereof based on the total amount of the lubricating oil composition, the above-mentioned neutralization effect could not be sufficiently exhibited and therefore the composition is poor in oxidation stability and heat resistance.
  • the content of the alkaline earth metal-based detergent (C) is more than 2,700 ppm by mass in terms of an alkaline earth metal atom thereof, the metal amount in the composition may increase to form nuclei for sludge formation, and the composition is poor in heat resistance.
  • the content of the alkaline earth metal-based detergent (C) is, in terms of an alkaline earth metal atom thereof based on the total amount of the lubricating oil composition, preferably 1,800 ppm by mass or more and 2,600 ppm by mass or less, more preferably 1,900 ppm by mass or more and 2,500 ppm by mass or less, even more preferably 2,000 ppm by mass or more and 2,500 ppm by mass or less.
  • alkaline earth metal-based detergent (C) at least one selected from the group consisting of alkaline earth metal sulfonates, alkaline earth metal phenates and alkaline earth metal salicylates to be mentioned below may be used, and a mixture of two or more of them may also be used. Above all, alkaline earth metal sulfonates are preferred from the viewpoint of heat resistance.
  • the alkaline earth metal sulfonate includes alkaline earth metal salts, especially magnesium salts and/or calcium salts of alkylaromatic sulfonic acids obtained by sulfonating an alkylaromatic compound having a molecular weight of 300 to 1,500, preferably 400 to 700. Above all, using calcium salts is preferred.
  • the alkaline earth metal phenate includes alkaline earth metal salts, especially magnesium salts and/or calcium salts of an alkylphenol, an alkylphenol sulfide or a Mannich reaction product of an alkylphenol, and above all, calcium salts are especially preferred.
  • the alkaline earth metal salicylate includes alkaline earth metal salts, especially magnesium salts and/or calcium salts of an alkylsalicylic acid, and above all, calcium salts are preferred.
  • the carbon number of the alkyl group constituting the alkaline earth metal-based detergent (C) is preferably 4 to 30, more preferably 6 to 18, and the alkyl group may be linear or branched.
  • the alkyl group may be any of a primary alkyl group, a secondary alkyl group or a tertiary alkyl group.
  • the alkaline earth metal sulfonate, the alkaline earth metal phenate and the alkaline earth metal salicylate may be any of neutral, basic or overbased ones.
  • the neutral alkaline earth metal salts include neutral alkaline earth metal sulfonates, neutral alkaline earth metal phenates and neutral alkaline earth metal salicylates to be obtained by directly reacting the above-mentioned alkylaromatic sulfonic acid, alkylphenol, alkylphenol sulfide, Mannich reaction product of an alkylphenol, or an alkylsalicylic acid with an alkaline earth metal base such as an oxide or hydroxide of an alkaline earth metal of magnesium and/or calcium, or once converting into an alkali metal salt, such as a sodium salt and a potassium salt, and then substituting with an alkaline earth metal salt.
  • Examples of the basic alkaline earth metal salt include basic alkaline earth metal sulfonates, basic alkaline earth metal phenates and basic alkaline earth metal salicylates to be obtained by heating the above-mentioned neutral alkaline earth metal sulfonate, neutral alkaline earth metal phenate or neutral alkaline earth metal salicylate with an excessive amount of an alkaline earth metal salt or an alkaline earth metal base in the presence of water.
  • overbased alkaline earth metal salt examples include overbased alkaline earth metal sulfonates, overbased alkaline earth metal phenates and overbased alkaline earth metal salicylates to be obtained by reacting the above-mentioned neutral alkaline earth metal sulfonate, neutral alkaline earth metal phenate or neutral alkaline earth metal salicylate with an alkaline earth metal carbonate or borate in the presence of carbon dioxide.
  • the alkaline earth metal-based detergent (C) is generally sold on the market in a form thereof diluted with a light lubricant base oil or the like and is therefore available, and in general, those having a metal content of 1.0 to 20% by mass, preferably 2.0 to 16% by mass are preferred.
  • the metal ratio in the alkaline earth metal-based detergent (C) in this embodiment is not specifically limited, and one or more having a metal ratio of 20 or less may be used singly or in combination.
  • the metal ratio is preferably 3 or less, more preferably 1.5 or less, even more preferably 1.2 or less from the viewpoint of securing excellent oxidation stability, base number retention and heat resistance at high temperatures.
  • the metal ratio as referred to herein is represented by [valence of metal element ⁇ metal element content (mol%)/soap group content (mol%)] in a metal-based detergent, and the metal element includes calcium and magnesium, the soap group includes a sulfonic acid group, a phenol group and a salicylic acid group.
  • the alkaline earth metal-based detergent (C) may be any of the above-mentioned neutral, basic or overbased ones, and examples thereof include an alkaline earth metal-based detergent (C) generally having a base number of 10 mgKOH/g or more and 500 mgKOH/g or less, preferably 15 mgKOH/g or more and 450 mgKOH/g or less, and one or more of these may be used singly or in combination.
  • basic or overbased ones are more preferred, and those having a base number of 150 mgKOH/or or more and 450 mgKOH/g or less are preferred.
  • Those having a base number of 150 mgKOH/or or more and 450 mgKOH/g or less can exhibit more excellent oxidation stability and are also excellent in heat resistance.
  • the base number of the alkaline earth metal-based detergent (C) as referred to in this description is one measured according to the perchloric acid method of JIS K2501:2003.
  • the base number of the alkaline earth metal-based detergent (C) is more preferably 200 mgKOH/or or more and 450 mgKOH/g or less, even more preferably 250 mgKOH/or or more and 400 mgKOH/g or less.
  • the alkaline earth metal atom contained in the alkaline earth metal-based detergent (C) is one or more selected from a beryllium atom, a magnesium atom, a calcium atom, a strontium atom and a barium atom, and from the viewpoint of high-temperature heat resistance, calcium, magnesium or barium is preferred, calcium or magnesium is more preferred, and calcium is even more preferred.
  • a calcium sulfonate is preferably used as the alkaline earth metal-based detergent (C).
  • the lubricating oil composition of this embodiment may contain a polymer (D) having a mass average molecular weight of more than 5,000.
  • the content of the polymer (D) is preferably less than 50 parts by mass relative to 100 parts by mass of the olefin oligomer (A).
  • the proportion to 100 parts by mass of the olefin oligomer (A) falls within the above range, the composition can maintain heat resistance in, for example, high-temperature parts of transmissions.
  • the amount of the polymer (D) falls within the above range, viscosity lowering in actual vehicle driving owing to shear of the polymer compound can be suppressed as much as possible.
  • the content of the polymer (D) is more preferably less than 30 parts by mass relative to 100 parts by mass of the olefin oligomer (A), even more preferably less than 20 parts by mass.
  • the mass average molecular weight of the polymer (D) is preferably 120,000 or less, more preferably 50,000 or less, even more preferably 40,000 or less.
  • the polymer (D) is not specifically limited, and any polymethacrylates and the like generally usable as a pour point depressant can be used. Even though not containing a viscosity index improver, the lubricating oil composition of this embodiment can still maintain a stable oil film strength even at high temperatures though, and therefore the composition is not needed to contain a viscosity index improver. Even in the case where the polymer (D) grouped in the category of a viscosity index improver is contained, the lubricating oil composition can still realize excellent shear stability when the content of the polymer falls within the above-mentioned mass ratio.
  • the lubricating oil composition of this embodiment may contain a zinc dithiophosphate (E).
  • E zinc dithiophosphate
  • those represented by the following general formula (E-1) are usable.
  • R 4 to R 7 each independently represent a group selected from a linear, branched or cyclic alkyl group having 1 to 24 carbon atoms, and a linear, branched or cyclic alkenyl group having 1 to 24 carbon atoms.
  • R 4 to R 7 each independently represent a linear, branched or cyclic alkyl group having 1 to 24 carbon atoms, or a linear, branched or cyclic alkenyl group having 1 to 24 carbon atoms, and they may be the same as or different from each other, but from the viewpoint of easiness in production, they are preferably the same.
  • R 4 to R 7 are preferably linear, and R 4 to R 7 each are preferably an alkyl group.
  • the alkyl group for R 4 to R 7 includes a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, a nonyl group, a decyl group, an undecyl group, a dodecyl group, a tridecyl group, a tetradecyl group, a pentadecyl group, a hexadecyl group, a heptadecyl group, an octadecyl group, a nonadecyl group, an eicosyl group, a heneicosyl group, a docosyl group, a tricosyl group and a tetracosyl group, and these may be linear, branched or cyclic.
  • the alkenyl group includes a vinyl group, a propenyl group, a butenyl group, a pentenyl group, a hexenyl group, a heptenyl group, an octenyl group, a nonenyl group, a decenyl group, an undecenyl group, a dodecenyl group, a tridecenyl group, a tetradecenyl group, a pentadecenyl group, a hexadecenyl group, a heptadecenyl group, an octadecenyl group, a nonadecenyl group, an eicosenyl group, a heneicosenyl group, a docosenyl group, a tricosenyl group, and a tetracosenyl group, and these may be linear, branched or cyclic
  • the content thereof is, based on the total amount of the lubricating oil composition, generally 0.05% by mass or more and 5% by mass or less, preferably 0.1% by mass or more and 3% by mass or less, more preferably 1% by mass or more and 2.5% by mass or less.
  • the friction coefficient ( ⁇ ) may be improved in gear change to better shift feeling.
  • the base oil for use in this embodiment may be any of a mineral oil or a synthetic oil, and a mixed oil of a mineral oil and a synthetic oil may also be used.
  • mineral oil examples include topped crudes obtained through atmospheric distillation of crude oils such as paraffin base crude oils, mixed crude oils, and naphthene base crude oils; distillates obtained through vacuum distillation of such topped crudes; purified oils obtained by purifying the distillates through one or more purification treatments of solvent deasphalting, solvent extraction, hydrocracking, solvent dewaxing, catalytic dewaxing or hydrorefining, and waxes.
  • mineral oils grouped in Group 2 or 3 in the base oil category of API are preferred.
  • those grouped in Group 3 are more preferred.
  • the base oil grouped in Group 2 has a saturation content of 90% or more, a sulfur content of 0.03% or less, and a viscosity index of from 80 to less than 120.
  • the base oil grouped in Group 3 has a saturation content of 90% or more, a sulfur content of 0.03% or less, and a viscosity index of 120 or more.
  • the sulfur content is a value measured according to JIS K2541-6:2013; the saturation content is a value measured according to ASTM D 2007. Further, the viscosity index is a value measured according to JIS K 2283:2000.
  • the synthetic oil includes various esters such as polyol esters, dibasic acid esters (for example, ditridecyl glutarate), tribasic acid esters (for example, 2-ethylhexyl trimellitate), and phosphates; various ethers such as polyphenyl ethers; polyalkylene glycols; alkylbenzenes; alkylnaphthalenes; and synthetic oils obtained through isomerization of wax (GTL (gas-to-liquid wax)) produced in Fischer-Tropsch synthesis.
  • esters such as polyol esters, dibasic acid esters (for example, ditridecyl glutarate), tribasic acid esters (for example, 2-ethylhexyl trimellitate), and phosphates
  • various ethers such as polyphenyl ethers
  • polyalkylene glycols alkylbenzenes
  • alkylnaphthalenes alkylnaphthalenes
  • one of these base oils may be used alone or two or more kinds thereof may be used in combination.
  • the kinematic viscosity at 100°C of the base oil for use in this embodiment is preferably 2.0 mm 2 /s or more and 30 mm 2 /s or less, more preferably 2.5 mm 2 /s or more and 25 mm 2 /s or less, even more preferably 3.0 mm 2 /s or more and 20 mm 2 /s or less.
  • the viscosity index of the base oil for use in this embodiment is, from the viewpoint of providing a lubricating oil composition capable of preventing viscosity change with temperature change and capable of improving fuel saving performance, preferably 80 or more, more preferably 90 or more, even more preferably 120 or more.
  • the kinematic viscosity and the viscosity index of the mixed oil each fall within the above-mentioned range.
  • the content of the base oil is, based on the total amount of the composition, preferably 75% by mass or more, more preferably 80% by mass or more, even more preferably 85% by mass or more, and is preferably 97% by mass or less, more preferably 95% by mass or less.
  • the lubricating oil composition for transmissions of this embodiment may contain additives such as a friction modifier, a dispersant and an anti-foaming agent.
  • additives such as a friction modifier, a dispersant and an anti-foaming agent.
  • a pour point depressant is grouped in the polymer (D) having a mass average molecular weight of more than 5,000, and is not included in the other additives.
  • the amount of the additive to be blended is, based on the total amount of the composition, preferably 10% by mass or less, more preferably 7.5% by mass or less, even more preferably 5.0% by mass or less.
  • the kinematic viscosity at 100°C of the lubricating oil composition of this embodiment is 4.0 mm 2 /s or more and 6.0 mm 2 /s or less.
  • the oil film strength lowers therefore resulting in lowering of seizure resistance, wear resistance and fatigue resistance.
  • the kinematic viscosity at 100°C is more than 6.0 mm 2 /s, resistance to stirring increases, which is unfavorable in point of fuel saving performance.
  • the kinematic viscosity at 100°C of the lubricating oil composition of this embodiment is more preferably 4.5 mm 2 /s or more and 5.8 mm 2 /s or less, even more preferably 4.6 mm 2 /s or more and 5.5 mm 2 /s or less
  • the lubricating oil composition of this embodiment can be favorably used for transmissions.
  • the lubricating oil composition of this embodiment has a low viscosity, therefore preventing viscosity lowering in actual vehicle driving, and is excellent in heat resistance and oxidation stability. Consequently, in down-sized and weight-reduced transmissions, for example, the composition can prevent sludge adhesion to a synchromesh mechanism, therefore securing good shift feeling. In addition, the composition can keep good synchronizer ring operation. Accordingly, this embodiment also provides a lubrication method using the lubricating oil composition mentioned above and a use method for the composition.
  • this embodiment can provide a transmission loaded with the lubricating oil composition.
  • the lubricating oil composition of this embodiment can be produced by blending (A) an olefin oligomer having a mass average molecular weight of 500 or more and 5,000 or less, (B) an antioxidant containing (B-1) a phenol-based antioxidant and (B-2) an amine-based antioxidant, and (C) an alkaline earth metal-based detergent, in a base oil, wherein the alkaline earth metal-based detergent (C) is blended such that the content of the alkaline earth metal-based detergent (C) is 1,700 ppm by mass or more and 2,700 ppm by mass or less in terms of an alkaline earth metal atom thereof based on the total amount of the lubricating oil composition.
  • the kinematic viscosity at different temperatures was measured according to JIS K2283:2000.
  • the content of each component was measured according to the following methods.
  • each sample was tested under the condition of a panel temperature of 300°C and an oil temperature of 100°C, in a cycle of a splashing time of 15 seconds and a stop time of 45 seconds for 3 hours. After the test, the weight of coke having adhered to the panel (mg) was measured.
  • the kinematic viscosity at 100°C before and after a shear test was measured, and the shear stability was calculated according to the following equation.
  • the shear test was carried out based on the ultrasonic method A (JPI-5S-29-06) under the condition of an ultrasonic irradiation time of 60 minutes, at room temperature and an oil amount of 30 cc.
  • the output voltage for ultrasonic waves in the shear stability test was controlled such that, after 30 cc of a standard oil was irradiated with ultrasonic waves for 10 minutes, the kinematic viscosity reduction at 100°C was 25%.
  • Shear stability % kinematic viscosity before test ⁇ kinematic viscosity after test / kinematic viscosity before test ⁇ 100
  • Tables 1 and 2 The components shown in Tables 1 and 2 were blended to prepare lubricating oil compositions.
  • the lubricating oil compositions prepared in Examples and Comparative Examples were analyzed to determine the acid value, the 40°C kinematic viscosity, the 100°C kinematic viscosity, the calcium content, the nitrogen content, the phosphorus content and the sulfur content before the test, and then these compositions were tested as in the above-mentioned (I) to (III). All the results are shown in Tables.
  • the lubricating oil compositions of Examples 1 to 6 have a low kinematic viscosity at 100°C and are excellent in heat resistance and oxidation stability.
  • these compositions do not require a polymer having a high molecular weight such as a viscosity index improver to cause viscosity reduction by shearing, the viscosity lowering percentage thereof is low even after a shear test, and it is known that the compositions can sufficiently prevent viscosity reduction in actual vehicle driving.
  • Comparative Example 5 an oligomer having a mass average molecular weight of 17,000 is used, and therefore shear stability is poor. From Comparative Examples 6 and 7, it is known that, when a phenol-based antioxidant and an amine-based antioxidant are not used in combination as the antioxidant (B), heat resistance is also poor.
  • a lubricating oil composition capable of attaining viscosity reduction and capable of preventing viscosity lowering in actual vehicle driving, and capable of attaining improved heat resistance and oxidation stability accompanied by down-sizing and weight-saving of devices.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)
  • General Details Of Gearings (AREA)
EP17760169.7A 2016-03-04 2017-03-03 Lubricating oil composition Active EP3425032B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2016042777 2016-03-04
PCT/JP2017/008496 WO2017150707A1 (ja) 2016-03-04 2017-03-03 潤滑油組成物

Publications (3)

Publication Number Publication Date
EP3425032A1 EP3425032A1 (en) 2019-01-09
EP3425032A4 EP3425032A4 (en) 2019-08-07
EP3425032B1 true EP3425032B1 (en) 2021-01-27

Family

ID=59742968

Family Applications (1)

Application Number Title Priority Date Filing Date
EP17760169.7A Active EP3425032B1 (en) 2016-03-04 2017-03-03 Lubricating oil composition

Country Status (4)

Country Link
EP (1) EP3425032B1 (zh)
JP (1) JP6913075B2 (zh)
CN (1) CN108699484B (zh)
WO (1) WO2017150707A1 (zh)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20190127656A1 (en) * 2017-10-31 2019-05-02 Exxonmobil Research And Engineering Company Lubricant compositions comprising polymeric diphenylamine antioxidants
US20190144776A1 (en) * 2017-10-31 2019-05-16 Exxonmobil Research And Engineering Company Lubricant grease compositions comprising polymeric diphenylamine antioxidants

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1121681A (en) * 1965-08-31 1968-07-31 Lubrizol Corp Compositions containing substituted succinic acid derivatives
JP2608098B2 (ja) * 1988-05-13 1997-05-07 出光興産株式会社 潤滑油組成物
JPH04202398A (ja) * 1990-11-30 1992-07-23 Tonen Corp 潤滑油組成物
US5756429A (en) * 1993-10-06 1998-05-26 Idemitsu Kosan Co., Ltd. Lubricating oil composition for high-speed gear
WO2004069967A1 (ja) * 2003-02-07 2004-08-19 Nippon Oil Corporation 変速機用潤滑油組成物
JP4806528B2 (ja) * 2004-12-22 2011-11-02 出光興産株式会社 内燃機関用潤滑油組成物
EP2333034B1 (en) * 2005-11-15 2016-01-27 Idemitsu Kosan Co., Ltd. Transmission fluid composition
JP5350583B2 (ja) * 2006-08-03 2013-11-27 出光興産株式会社 潤滑油組成物及びそれを用いた自動車変速機の金属疲労の向上方法
US20080182767A1 (en) * 2007-01-29 2008-07-31 Loper John T Compounds and Lubricating Compositions Containing the Compounds
JP2010047747A (ja) * 2008-07-22 2010-03-04 Sanyo Chem Ind Ltd 潤滑油添加剤及び潤滑油組成物
JP5683914B2 (ja) * 2010-11-18 2015-03-11 出光興産株式会社 潤滑油組成物
US8796189B2 (en) * 2011-10-14 2014-08-05 Chevron U.S.A. Inc. Gear lubricant
WO2013093103A1 (en) * 2011-12-22 2013-06-27 Shell Internationale Research Maatschappij B.V. Lubricating composition
JP5930904B2 (ja) * 2012-07-27 2016-06-08 Jxエネルギー株式会社 潤滑油組成物
JP5930905B2 (ja) * 2012-07-27 2016-06-08 Jxエネルギー株式会社 潤滑油組成物
JP6302458B2 (ja) * 2013-03-08 2018-03-28 出光興産株式会社 潤滑油組成物
US20150051129A1 (en) * 2013-08-15 2015-02-19 Infineum International Limited Transmission Fluid Compositions for Improved Energy Efficiency
US20180051228A1 (en) * 2015-03-31 2018-02-22 Idemitsu Kosan Co., Ltd. Lubricating oil composition for four stroke engine

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
None *

Also Published As

Publication number Publication date
CN108699484B (zh) 2022-01-11
EP3425032A1 (en) 2019-01-09
CN108699484A (zh) 2018-10-23
JP6913075B2 (ja) 2021-08-04
WO2017150707A1 (ja) 2017-09-08
EP3425032A4 (en) 2019-08-07
JPWO2017150707A1 (ja) 2018-12-27

Similar Documents

Publication Publication Date Title
EP3279298B1 (en) Lubricating oil composition and method for reducing friction in internal combustion engines
CN108884405B (zh) 润滑油组合物
EP3511398A1 (en) Gasoline engine lubricant oil composition and manufacturing method therefor
EP3872149B1 (en) Lubricant composition and method for producing same
US11193080B2 (en) Lubricating oil composition
EP3388500A1 (en) Lubricant composition
EP3425032B1 (en) Lubricating oil composition
EP2837677B1 (en) Lubricating oil composition
CN117098831A (zh) 润滑油组合物
EP4317370A1 (en) Lubricant composition
JP2019089918A (ja) 緩衝器用潤滑油組成物
EP4177323A1 (en) Lubricating oil composition, shock absorber, and method for using lubricating oil composition
JP5122353B2 (ja) ウォームギヤ油組成物およびウォームギヤユニット
EP4001382B1 (en) Lubricating oil composition
JP2019147864A (ja) 潤滑油組成物
EP4310165A1 (en) Lubricant composition
EP4289919A1 (en) Lubricant composition
EP4269546A1 (en) Lubricant composition
EP4368688A1 (en) Lubricant composition
EP4317371A1 (en) Lubricating oil composition
JP2021161291A (ja) 潤滑油組成物

Legal Events

Date Code Title Description
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE

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

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

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

17P Request for examination filed

Effective date: 20181001

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

DAV Request for validation of the european patent (deleted)
DAX Request for extension of the european patent (deleted)
A4 Supplementary search report drawn up and despatched

Effective date: 20190709

RIC1 Information provided on ipc code assigned before grant

Ipc: C10N 20/02 20060101ALI20190703BHEP

Ipc: C10M 167/00 20060101ALI20190703BHEP

Ipc: C10N 10/04 20060101AFI20190703BHEP

Ipc: C10N 20/00 20060101ALI20190703BHEP

Ipc: C10N 20/04 20060101ALI20190703BHEP

Ipc: C10N 30/02 20060101ALI20190703BHEP

Ipc: C10N 40/04 20060101ALI20190703BHEP

Ipc: C10N 30/10 20060101ALI20190703BHEP

Ipc: C10N 30/08 20060101ALI20190703BHEP

REG Reference to a national code

Ref country code: DE

Ref legal event code: R079

Ref document number: 602017032119

Country of ref document: DE

Free format text: PREVIOUS MAIN CLASS: C10M0169040000

Ipc: C10N0010040000

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

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

Free format text: STATUS: GRANT OF PATENT IS INTENDED

RIC1 Information provided on ipc code assigned before grant

Ipc: C10N 30/04 20060101ALN20200813BHEP

Ipc: C10N 40/04 20060101ALI20200813BHEP

Ipc: C10N 30/00 20060101ALN20200813BHEP

Ipc: C10N 30/08 20060101ALI20200813BHEP

Ipc: C10N 20/02 20060101ALI20200813BHEP

Ipc: C10N 20/00 20060101ALI20200813BHEP

Ipc: C10N 30/02 20060101ALI20200813BHEP

Ipc: C10N 20/04 20060101ALI20200813BHEP

Ipc: C10N 30/10 20060101ALI20200813BHEP

Ipc: C10N 10/04 20060101AFI20200813BHEP

Ipc: C10M 167/00 20060101ALI20200813BHEP

INTG Intention to grant announced

Effective date: 20200901

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

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

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 1358357

Country of ref document: AT

Kind code of ref document: T

Effective date: 20210215

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602017032119

Country of ref document: DE

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20210127

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG9D

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 1358357

Country of ref document: AT

Kind code of ref document: T

Effective date: 20210127

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

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210127

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210127

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210428

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210527

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210427

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210427

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210127

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

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210127

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210127

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210127

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210127

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210127

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

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210527

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602017032119

Country of ref document: DE

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

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210127

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210127

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210127

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210127

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

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

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210127

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210127

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210127

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

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20210331

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20210427

26N No opposition filed

Effective date: 20211028

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

Ref country code: IE

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

Effective date: 20210303

Ref country code: GB

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

Effective date: 20210427

Ref country code: LU

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

Effective date: 20210303

Ref country code: LI

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

Effective date: 20210331

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210127

Ref country code: CH

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

Effective date: 20210331

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210127

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

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210127

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

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210127

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

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210527

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

Ref country code: BE

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

Effective date: 20210331

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

Ref country code: FR

Payment date: 20230208

Year of fee payment: 7

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

Ref country code: DE

Payment date: 20230131

Year of fee payment: 7

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

Ref country code: NL

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

Effective date: 20210127

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210127

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

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20170303

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

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210127

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

Ref country code: TR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210127

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

Ref country code: MT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20210127