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WO2007129775A1 - Composition de graisse pour joints homocinétiques - Google Patents

Composition de graisse pour joints homocinétiques Download PDF

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Publication number
WO2007129775A1
WO2007129775A1 PCT/JP2007/059992 JP2007059992W WO2007129775A1 WO 2007129775 A1 WO2007129775 A1 WO 2007129775A1 JP 2007059992 W JP2007059992 W JP 2007059992W WO 2007129775 A1 WO2007129775 A1 WO 2007129775A1
Authority
WO
WIPO (PCT)
Prior art keywords
group
constant velocity
molybdenum
grease
weight
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.)
Ceased
Application number
PCT/JP2007/059992
Other languages
English (en)
Inventor
Takahiro Ozaki
Kouichi Numazawa
Shinichi Takabe
Takaaki Shibata
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.)
NTN Corp
Showa Shell Sekiyu KK
Original Assignee
NTN Corp
Showa Shell Sekiyu KK
NTN Toyo Bearing 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 NTN Corp, Showa Shell Sekiyu KK, NTN Toyo Bearing Co Ltd filed Critical NTN Corp
Priority to BRPI0711343-9A priority Critical patent/BRPI0711343A2/pt
Priority to EP07743427A priority patent/EP2054491A4/fr
Priority to US12/296,816 priority patent/US20090176671A1/en
Priority to AU2007246315A priority patent/AU2007246315A1/en
Priority to MX2008014236A priority patent/MX2008014236A/es
Priority to CN2007800141510A priority patent/CN101432408B/zh
Publication of WO2007129775A1 publication Critical patent/WO2007129775A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16DCOUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
    • F16D3/00Yielding couplings, i.e. with means permitting movement between the connected parts during the drive
    • F16D3/16Universal joints in which flexibility is produced by means of pivots or sliding or rolling connecting parts
    • 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
    • C10M135/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
    • C10M135/12Thio-acids; Thiocyanates; Derivatives thereof
    • C10M135/14Thio-acids; Thiocyanates; Derivatives thereof having a carbon-to-sulfur double bond
    • 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
    • C10M137/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
    • C10M137/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having no phosphorus-to-carbon bond
    • C10M137/04Phosphate esters
    • C10M137/10Thio derivatives
    • 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
    • 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
    • C10M2215/225Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
    • C10M2215/226Morpholines
    • 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
    • C10M2217/00Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2217/04Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2217/045Polyureas; Polyurethanes
    • C10M2217/0456Polyureas; Polyurethanes 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
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/044Sulfonic acids, Derivatives thereof, e.g. neutral salts
    • 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
    • C10M2219/06Thio-acids; Thiocyanates; Derivatives thereof
    • C10M2219/062Thio-acids; Thiocyanates; Derivatives thereof having carbon-to-sulfur double bonds
    • C10M2219/066Thiocarbamic type compounds
    • C10M2219/068Thiocarbamate metal 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
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • C10M2219/104Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
    • 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
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/12Groups 6 or 16
    • 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
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/04Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
    • C10N2040/046Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for traction drives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/10Form in which the lubricant is applied to the material being lubricated semi-solid; greasy
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16DCOUPLINGS FOR TRANSMITTING ROTATION; CLUTCHES; BRAKES
    • F16D2300/00Special features for couplings or clutches
    • F16D2300/06Lubrication details not provided for in group F16D13/74

Definitions

  • the present invention relates to a grease composition for constant velocity joints suitable for use at the lubrication points of constant velocity joints in automobiles .
  • lithium soap greases which contain molybdenum disulphide and extreme-pressure lithium soap greases which contain sulphur-phosphorus type additives have been used as greases for constant velocity joints.
  • low-wear and temperature-resistant greases for high-temperature use in which urea compounds or lithium complex soaps are used as the thickener and where organomolybdenum compounds are added have since become commonly used.
  • the present invention provides a grease for use in constant velocity joints which improves on the aforementioned greases, which reduces wear. in constant velocity joints, which inhibits the flaking due to metal fatigue and which further has excellent durability.
  • durability tests were carried out by adding various additives to a low-wear urea grease in which (A) a molybdenum dialkyldithiocarbamate and (B) a molybdenum dithiophosphate were used together, and by using wear- resistance tests by means of an SRV test rig and actual constant velocity joints. Flaking-resistance performance was evaluated, and as a result perfection of the present invention was achieved.
  • the present invention provides a grease for use in constant velocity joints which incorporates in a urea grease (A) a molybdenum dialkyldithiocarbamate as represented by the undermentioned formula I, (B) a molybdenum dithiophosphate as represented by the undermentioned formula II, (C) 2- (4-morpholinyldithio) benzothiazole as represented by the undermentioned formula III and (D) a calcium sulphonate.
  • A a molybdenum dialkyldithiocarbamate as represented by the undermentioned formula I
  • B a molybdenum dithiophosphate
  • C 2- (4-morpholinyldithio) benzothiazole as represented by the undermentioned formula III
  • D a calcium sulphonate.
  • R is a primary or secondary alkyl group or an aryl group
  • the blending is such that the total of the aforementioned (A) and (B) is not more than 10% by weight, (C) is not more than 3% by weight and (D) is not more than 3% by weight.
  • a grease for use in constant velocity joints is provided by further incorporating not more than 3% by weight of (E) a zinc dithiophosphate as represented by the undermentioned formula IV.
  • R' is a primary or secondary alky group or an aryl group
  • the present invention provides the use of the grease composition in constant velocity joints, preferably in automobiles.
  • the urea compound adheres to the metal surfaces, iron oxide or iron sulphide is formed in the lower layer thereof, making a solid film, and so it is possible to offer a grease for use in constant velocity joints which reduces wear in the constant velocity joints and which also inhibits the phenomenon of flaking due to the accompanying metal fatigue, and which has excellent durability.
  • the base oil of the invention it is possible to use e.g. mineral oils, plant oils and synthetic oils such as ester oils, ether oils and hydrocarbon oils, or mixtures thereof.
  • urea compounds such as monoureas, diureas, triureas and tetraureas.
  • diurea compounds obtained by reaction of diisocyanates and monoamines there are diurea compounds obtained by reaction of diisocyanates and monoamines, and tetraurea compounds obtained by reaction of diisocyanates, monoamines and diamines.
  • diisocyanates mention may be made of diphenylmethane diisocyanate, tolylene diisocyanate, bitolylene diisocyanate and naphthylene diisocyanate.
  • monoamines mention may be made of octylamine, dodecylamine, stearylamine, oleylamine, aniline, p-toluidine and cyclohexylamine.
  • diamines mention may be made of ethylenediamine, propanediamine, butanediamine and phenylenediamine .
  • the molybdenum dialkyldithiocarbamates as represented by aforementioned formula (I) and which are the aforementioned constituent (A) have alkyl groups of 1 - 24 carbons as their R, and preferably have alkyl groups of 3 ⁇ 18 carbons.
  • sulphurised molybdenum diethyldithiocarbamate sulphurised molybdenum dipropyldithiocarbamate, sulphurised molybdenum dibutyldithiocarbamate, sulphurised molybdenum dipentyldithiocarbamate, sulphurised molybdenum dihexyldithiocarbamate, sulphurised molybdenum dioctyldithiocarbamate, sulphurised molybdenum didecyldithiocarbamate, sulphurised molybdenum didodecyl dithiocarbamate, sulphurised molybdenum di (butylphenyl) dithiocarbamate, sulphurised molybdenum di (nonylphenyl) dithiocarbamate, sulphurised oxymolybdenum
  • molybdenum dithiophosphates as represented by aforementioned formula (II) and which are the aforementioned constituent (B) mention may be made of sulphurised molybdenum diethyldithiophosphate, sulphurised molybdenum dipropyldithiophosphate, sulphurised molybdenum dibutyldithiophosphate, s ⁇ lphurised molybdenum dipentyldithiophosphate, sulphurised molybdenum dihexyldithiophosphate, sulphurised molybdenum dioctyldithiophosphate, sulphurised molybdenum didecyldithiophosphate, sulphurised molybdenum didodecyldithiophosphate, sulphurised molybdenum di (butylphenyl) dithiophosphate, sulphurised molybdenum di (butyl
  • the aforementioned component (D) is an ordinary calcium sulphonate.
  • Examples are the calcium salt of petroleum sulphonic acid, the calcium salt of an alkyl aromatic sulphonic acid, the overbased calcium salt of petroleum sulphonic acid and the overbased calcium salt of an alkyl aromatic sulphonic acid. It is possible to use these singly or in mixtures.
  • This component (D) functions as a dispersant, controls wear resistance and further contributes an improvement in durability.
  • the zinc dithiophosphates as represented by the aforementioned formula (IV) and which are the aforementioned component (E) are zinc dialkyl dithiophosphates or zinc diaryldithiophosphates .
  • R 1 denotes a primary or secondary alkyl group or an aryl group.
  • it may be a methyl group, ethyl group, propyl group, isopropyl group, butyl group, secondary butyl group, isobutyl group, pentyl group, 4-methylpentyl group, hexyl group, 2-ethylhexyl group, heptyl group, octyl group, nonyl group, decyl group, isodecyl group, dodecyl group, tetradecylgroup, hexadecyl group, octadecyl group, eicosyl group, docosyl group, tetracosyl group, cyclopentyl group, cyclohexyl group, methylcyclohexyl group, ethylcyclohexyl group, dimethylcyclohexyl group,
  • Each of these R 1 may be the same or different.
  • secondary alkyl zinc dithiophosphates mention may be made of mono or di- sec-pentyl zinc dithiophosphate and mono or di-4-methyl- 2-pentyl zinc dithiophosphate.
  • aryl zinc dithiophosphates mention may be made of zinc di-para-dodecylphenol dithiophosphate, zinc diheptylphenol dithiophosphate and zinc di-para-nonylphenol dithiophosphate.
  • the amount of molybdenum dithiocarbamate which is component (A) and molybdenum dithiophosphate which is component (B) blended into the urea grease may be made such that it is not more than 10% by weight.
  • the amount of the aforementioned components (A) and (B) in the urea grease is greater than mentioned above, the effect is the same or may even be the reverse effect. Normally, an amount of 1 ⁇ 31 by weight of each of component (A) and component (B) is preferred.
  • the amount of 2- (4-morpholinyldithio) - benzothiazole which is component (C) in the grease is not more than 3% by weight. If it exceeds this, the effect is the same or may even be the reverse effect. Normally, 0.1 ⁇ 1% by weight is preferred.
  • the amount of calcium sulphonate which is component (D) in the grease may be made not more than 3% by weight. If it exceeds this, the effect is the same or may even be the reverse effect. Normally, 0.1 ⁇ 1% by weight is preferred.
  • the amount of this zinc dithiophosphate which is component (E) in the grease should be made not more than 3% by weight. If it exceeds this, the effect is the same or may even be the reverse effect. Normally, an excellent effect may be expected if it is made to be co-present preferably in the amount of 0.5 ⁇ 1% by weight.
  • the diurea grease was obtained by reacting 295.2 g diphenylmethane-4, 4 ' -diisocyanate and 304.8 g octylamine in 5400 g of a refined mineral oil with a kinetic viscosity at 100 0 C of approximately 15 mm 2 /s and evenly dispersing the diurea compound produced.
  • the content of the diurea compound was 10% by weight.
  • the penetration of this diurea grease 25°C, 60W) (JIS K2220) was 283.
  • the tetraurea grease was obtained by reacting 382.7 g diphenylmethane-4, 4' -diisocyanate, 411.4 g octylamine and 46 g ethylenediamine in 5160 g of a refined mineral oil with a kinetic viscosity at 100 0 C of approximately 15 mmVs and evenly dispersing the tetraurea compound produced.
  • the content of the tetraurea compound was 14% by weight.
  • the penetration of this tetraurea grease 25 0 C, 60W) (JIS K2220) was 285.
  • Molybdenum dialkyl dithiocarbamate (MoDTC) : "Sakuralube 600" (trade name, made by Asahi Denka
  • MoDTP (1) "Sakuralube 300" (trade name, made by Asahi Denka Kogyo Ltd.) was used.
  • MoDTP (2) "Molyvan L" (trade name, made by Vanderbilt Ltd.) was used.
  • Zinc dithiophosphate (ZnDTP) Zinc dithiophosphate
  • ZnDTP (1) "Lubrizol 1395" (trade name, made by Lubrizol Ltd.) was used.
  • ZnDTP (2) "Lubrizol 1371" (trade name, made by Lubrizol Ltd.) was used.
  • Calcium sulphonate Calcium salt of petroleum sulphonic acid.
  • each material was added to the diurea grease or tetraurea grease in the same way as for the aforementioned Examples, and after mixing and kneading in a three-roll mill and finishing to a uniform consistency, the constant velocity joint greases of Comparative Examples 1 - 10 were obtained. Evaluation tests
  • Test method A Birfield-type fixed joint (BJ) and a double offset plunging-type joint (DOJ) were packed with the test specimens, and their anti-flaking performance was evaluated by means of an actual test rig. Test conditions: • Speed 500 rpm

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • General Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Lubricants (AREA)

Abstract

La présente invention concerne une composition de graisse destinée à une utilisation pour des joints homocinétiques, ladite composition présentant des caractéristiques de résistance à l'usure et d'endurance améliorées. La graisse est fabriquée en incorporant dans une graisse à base d'urée (A) un dialkyldithiocarbamate de molybdène, (B) un dithiophosphate de molybdène, (C) un 2-(4-morpholinyldithio) benzothiazole et (D) un sulfonate de calcium. La quantité mélangée de (A) + (B) est inférieure ou égale à 10 % en poids et celle de (C) et (D) inférieure ou égale à 3 % en poids respectivement. L'invention concerne également une graisse destinée à une utilisation dans des joints homocinétiques, fabriquée en ajoutant en outre (E) du dithiophosphate de zinc aux composants (A) + (B) + (C) + (D) susmentionnés en une quantité mélangée inférieure ou égale à 3 % en poids.
PCT/JP2007/059992 2006-05-10 2007-05-09 Composition de graisse pour joints homocinétiques Ceased WO2007129775A1 (fr)

Priority Applications (6)

Application Number Priority Date Filing Date Title
BRPI0711343-9A BRPI0711343A2 (pt) 2006-05-10 2007-05-09 composições de graxa para juntas de velocidade constante
EP07743427A EP2054491A4 (fr) 2006-05-10 2007-05-09 Composition de graisse pour joints homocinétiques
US12/296,816 US20090176671A1 (en) 2006-05-10 2007-05-09 Grease Composition For Constant Velocity Joints
AU2007246315A AU2007246315A1 (en) 2006-05-10 2007-05-09 Grease composition for constant velocity joints
MX2008014236A MX2008014236A (es) 2006-05-10 2007-05-09 Composicion de grasa para las juntas de velocidad constante.
CN2007800141510A CN101432408B (zh) 2006-05-10 2007-05-09 等速万向节用润滑脂组合物

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2006131320A JP5379343B2 (ja) 2006-05-10 2006-05-10 等速ジョイント用グリース組成物
JP2006-131320 2006-05-10

Publications (1)

Publication Number Publication Date
WO2007129775A1 true WO2007129775A1 (fr) 2007-11-15

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2007/059992 Ceased WO2007129775A1 (fr) 2006-05-10 2007-05-09 Composition de graisse pour joints homocinétiques

Country Status (9)

Country Link
US (1) US20090176671A1 (fr)
EP (1) EP2054491A4 (fr)
JP (1) JP5379343B2 (fr)
KR (1) KR20090012207A (fr)
CN (1) CN101432408B (fr)
AU (1) AU2007246315A1 (fr)
BR (1) BRPI0711343A2 (fr)
MX (1) MX2008014236A (fr)
WO (1) WO2007129775A1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008028955A3 (fr) * 2006-09-08 2008-04-24 Shell Int Research Composition de graisse lubrifiante
WO2016155754A1 (fr) * 2015-03-31 2016-10-06 Gkn Driveline International Gmbh Composition de graisse destinée à être utilisée dans des joints homocinétiques

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6348374B2 (ja) * 2014-08-25 2018-06-27 シェルルブリカンツジャパン株式会社 グリース組成物
JP6480785B2 (ja) * 2015-04-03 2019-03-13 Ntn株式会社 グリース組成物
EP4004149A1 (fr) 2019-07-29 2022-06-01 Ecolab USA Inc. Complexes de molybdène solubles dans l'huile servant d'inhibiteurs d'encrassement à haute température
WO2021021891A1 (fr) 2019-07-29 2021-02-04 Ecolab Usa Inc. Complexes de molybdène solubles dans l'huile pour inhiber la corrosion à haute température et utilisations associées dans des raffineries de pétrole
CN116057155B (zh) * 2020-07-29 2025-08-29 埃科莱布美国股份有限公司 用于高温环烷酸腐蚀抑制的无磷油溶性钼络合物
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KR20230110495A (ko) * 2020-11-26 2023-07-24 교도유시 가부시끼가이샤 등속 조인트용 그리스 조성물
JPWO2023224006A1 (fr) * 2022-05-16 2023-11-23
JP2024170999A (ja) * 2023-05-29 2024-12-11 協同油脂株式会社 グリース組成物
KR102662782B1 (ko) 2023-06-13 2024-05-03 주식회사 라노스 하울링 방지 기능을 갖는 세라믹 식탁

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KR20090012207A (ko) 2009-02-02
CN101432408A (zh) 2009-05-13
EP2054491A1 (fr) 2009-05-06
CN101432408B (zh) 2012-04-04
AU2007246315A1 (en) 2007-11-15
BRPI0711343A2 (pt) 2011-08-30
MX2008014236A (es) 2008-11-14
JP2007302761A (ja) 2007-11-22
US20090176671A1 (en) 2009-07-09
EP2054491A4 (fr) 2011-01-12
JP5379343B2 (ja) 2013-12-25

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