EP0286139B1 - Lubrifiant ou concentré de lubrifiant - Google Patents

Lubrifiant ou concentré de lubrifiant Download PDF

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Publication number
EP0286139B1
EP0286139B1 EP88105725A EP88105725A EP0286139B1 EP 0286139 B1 EP0286139 B1 EP 0286139B1 EP 88105725 A EP88105725 A EP 88105725A EP 88105725 A EP88105725 A EP 88105725A EP 0286139 B1 EP0286139 B1 EP 0286139B1
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EP
European Patent Office
Prior art keywords
lubricant
weight
mpa
viscosity
oil
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.)
Expired - Lifetime
Application number
EP88105725A
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German (de)
English (en)
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EP0286139A1 (fr
Inventor
Gesellschaft für Industrielle Instandhaltungs- und Wartungsprodukte mbH SIWA
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.)
Bremer and Leguil GmbH
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Individual
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M161/00Lubricating compositions characterised by the additive being a mixture of a macromolecular compound and a non-macromolecular compound, each of these compounds being essential
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M101/00Lubricating compositions characterised by the base-material being a mineral or fatty oil
    • C10M101/02Petroleum fractions
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M101/00Lubricating compositions characterised by the base-material being a mineral or fatty oil
    • C10M101/04Fatty oil fractions
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    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/02Well-defined hydrocarbons
    • C10M105/06Well-defined hydrocarbons aromatic
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    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/08Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
    • C10M105/18Ethers, e.g. epoxides
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    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/08Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
    • C10M105/32Esters
    • C10M105/36Esters of polycarboxylic acids
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    • C10M105/00Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
    • C10M105/08Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
    • C10M105/32Esters
    • C10M105/38Esters of polyhydroxy compounds
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    • C10M107/00Lubricating compositions characterised by the base-material being a macromolecular compound
    • C10M107/02Hydrocarbon polymers; Hydrocarbon polymers modified by oxidation
    • C10M107/08Hydrocarbon polymers; Hydrocarbon polymers modified by oxidation containing butene
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    • C10M107/20Lubricating compositions characterised by the base-material being a macromolecular compound containing oxygen
    • C10M107/22Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M107/28Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate
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    • C10M107/20Lubricating compositions characterised by the base-material being a macromolecular compound containing oxygen
    • C10M107/30Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M107/32Condensation polymers of aldehydes or ketones; Polyesters; Polyethers
    • C10M107/34Polyoxyalkylenes
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    • C10M129/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
    • C10M129/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
    • C10M129/68Esters
    • C10M129/74Esters of polyhydroxy compounds
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    • C10M129/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
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    • C10M129/76Esters containing free hydroxy or carboxyl groups
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    • 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
    • C10M135/18Thio-acids; Thiocyanates; Derivatives thereof having a carbon-to-sulfur double bond thiocarbamic type, e.g. containing the groups
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    • C10M135/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
    • C10M135/32Heterocyclic sulfur, selenium or tellurium compounds
    • C10M135/36Heterocyclic sulfur, selenium or tellurium compounds the ring containing sulfur and carbon with nitrogen or oxygen
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    • 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
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    • 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
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    • 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
    • C10M141/10Lubricating 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 phosphorus-containing compound
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    • 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
    • C10M169/04Mixtures of base-materials and additives
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    • C10M169/04Mixtures of base-materials and additives
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    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/06Well-defined aromatic compounds
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    • C10M2203/065Well-defined aromatic compounds used as base material
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Definitions

  • the invention relates to a new lubricant or lubricant concentrate based on mineral oil and / or synthetic oil with improved lubricating properties, in particular improved load bearing, sliding and corrosion protection properties.
  • solid lubricants were developed which were introduced between the moving metal parts, such as graphite, MoS2, TiO2, Ca3 (PO4) 2, Teflon and the like, which were introduced as lubricious outer layers, suspensions, pastes or greases. Thereby the friction partners were better separated and their resilience increased. With centripetal movements of higher peripheral speed and at higher temperature, however, the solid lubricants and carrier media separate sooner or later due to their different specific densities. This limited the long-term lubrication. In a further step, it was possible to apply suitable metal cations to rubbing surfaces during operation from chemical complexes dissolved in a lubricant.
  • DE-PS 941 678 discloses lubricating oils containing soluble reaction products of phosphorus pentasulfide with liquid or solid aliphatic hydrocarbons or terpene hydrocarbons.
  • a lubricating oil is known which contains metal-containing alkylphenol sulfide esters in combination with zinc sulfonates.
  • DE-AS 1 444 892 a lubricating oil is known which contains a salt of an aromatic zinc dithiophosphate and a zinc carboxylic acid salt in the presence of water. While the first two products are lubricating oil detergents, the latter product is intended to prevent corrosion of silver bearing surfaces.
  • a lubricating oil which contains a salt of a substituted succinic acid, optionally together with a salt of an alkylated or esterified phosphoric acid. It is an antioxidant with a detergent effect.
  • a combination of dithiophosphate and dithiophosphinate salts is known from DE-AS 1 271 878.
  • From DE-OS 15 94 555 cutting oils containing free sulfur, a dialkyldithiophosphate and a chlorinated hydrocarbon are known.
  • Lubricating oils containing zinc or antimondithiocarbamate are known from US Pat. No. 3,462,367. Lubricating oils are known from US Pat. No.
  • Lubricating oil additives are also known from US Pat. No. 2,734,864, which are formed from a dithiophosphate of the alkaline earth metal salts in combination with a complex reaction product of phosphorus sulfides, wool fat and alcohol esters.
  • the undefined product contains considerable amounts of barium and zinc.
  • Such a lubricating oil additive cannot be used in practice because of its unbearable odor, which also endangers the people who come into contact with it.
  • lubricants based on mineral oil or synthetic oil which, in addition to the mineral or synthetic oil, contain an ester of an epoxidized fatty acid having 10 to 18 carbon atoms with mono- or polyhydric alcohols, an alkyl -, Aralkyl- or aryldithiophosphate of zinc, lead, tin, tungsten, molybdenum, niobium or lanthanum and optionally contain a sulfur phosphorus compound.
  • lubricants based on mineral or synthetic oil or lubricant concentrates which in addition to a lead, tungsten, molybdenum and / or vanadium dithiophosphate esterified with alkyl, aryl or aralkyl groups, also contain at least one zinc dialkyldithiophosphate and a metal-free sulfur-phosphorus compound.
  • These last-mentioned lubricants which have found widespread use, no longer meet all of the requirements placed on modern long-term and high-performance lubricants. Their coefficient of friction and abrasion are too high, their shelf life is inadequate in long-term use, and the complaint rate in the lubrication area is too high.
  • the object of the invention was therefore to create a new lubricant or lubricant concentrate based on mineral or synthetic oil, which is further improved with regard to its lubricating properties, in particular its friction and wear properties, thus noticeably reducing the energy and spare parts requirement and thus also meets the highest requirements.
  • the lubricants or lubricant concentrates according to the invention have significantly improved properties compared to the known lubricants or lubricant concentrates, in particular with regard to friction and wear, and thus have a reduced need for energy and spare parts. It is believed that this is due to the fact that when they are used in the rubbing and sliding area, metallic glass surfaces are formed from amorphously solidified metal melts, which no longer have metal crystal lattice structures.
  • the glass-like smooth friction and sliding surfaces which are presumably produced with the lubricant or lubricant concentrate according to the invention, significantly improve the entire lubrication process, since the coefficient of friction and with it the abrasion, oxidation and corrosion are significantly reduced.
  • the so-called fretting rust is also prevented by the lubricant or lubricant concentrate according to the invention.
  • the lubricants or lubricant concentrates according to the invention are extremely environmentally friendly since they contain no lead, no sulfurized whale sperm oil and hardly any phosphorus. This has been shown by fish tests and bacteria washing tests which were carried out with the lubricants or lubricant concentrates according to the invention. It was also found that they are 60% biodegradable in normal soil within 3 to 4 months, so that they can also be described as extremely environmentally friendly.
  • the quaternary carbon atom-containing polyol ester compounds used according to the invention are thermally very stable and therefore allow high operating temperatures of up to 300 ° C. They therefore open up the possibility of lifetime lubrication of highly loaded motors, turbines, rolling bearings, constant velocity joints and other high-performance machine elements.
  • lubricant or lubricant concentrate based on mineral and / or synthetic oil used here means both lubricating oils and lubricating greases based on mineral and / or synthetic oil.
  • Compounds containing quaternary carbon atoms are to be understood here as those compounds in which the four main valences of at least one carbon atom per molecule are occupied by four carbon atoms.
  • Such compounds are mono-, di- and trimeric pentaerythritol esters, other polyol esters, pentaerythritol ethoxy esters and telomeric acid pentaerythritol esters and the corresponding ethoxylated esters.
  • the lubricants or lubricant concentrates according to the invention have significantly improved properties compared to the known lubricants or lubricant concentrates, as the examples below show.
  • the glass-like smooth friction and sliding surfaces produced by the lubricant according to the invention save drive energy and lower the coefficient of friction per se and by building up a very adhesive boundary lubrication film which enables elastohydrodynamic lubrication even under point loads.
  • the friction temperature of the lubricant and lubrication point is reduced, the oxidation resistance of both is extended and the metallic friction partners are subjected to less specific alternating loads and temperatures. Overall, these effects greatly reduce wear and significantly increase the service life of the friction partners and the lubricant.
  • the lubricant or lubricant concentrate contains, as component (b), mono-, di- or tripentaerythritol, the alcoholic hydroxyl group (s) of which is preferably an unbranched or branched alkyl, aralkyl or aryl group having 6 to 18 carbon atoms 6 to 12 carbon atoms, in particular 8 to 12 carbon atoms, is (are) esterified or ethoxy-esterified.
  • component (b) mono-, di- or tripentaerythritol
  • the lubricant or lubricant concentrate additionally contains a component with at least one free hydroxyl group.
  • the lubricant or lubricant concentrate according to the invention contains component (b) in an amount of 0.1 to 40% by weight, preferably 0.1 to 20% by weight, in particular 1 to 12 % By weight, especially from 2 to 6% by weight, based on the weight of the mineral and / or synthetic oil.
  • the lubricant or lubricant concentrate according to the invention contains as component (b) an ester and / or ethoxylated ester derivative of mono-, di- or tripentaerythritol and / or a telomeric acid pentaerythritol ester or an ethoxylated derivative thereof.
  • the lubricant or lubricant concentrate according to the invention preferably contains beet oil, natural oil and / or a synthetic oil with a viscosity in the range from 1.0 mPa.s at 20 ° C. to 2.10 ° mPa.s at 20 ° C.
  • a mineral oil with a viscosity is particularly preferred from 1.0 mPa.s at 20 ° C to 540 mPa.s at 50 ° C as a natural oil and the use of an aromatic or aliphatic dicarboxylic acid ester, in particular poly- ⁇ -olefin-dicarboxylic acid ester, especially butyl ester, with a molecular weight in the range of 1000 to 3000, preferably of phthalic acid diisodecyl ester, trimethyladipic acid diidyl ester and sebacic acid diocyl ester, a polyisobutylene with a molecular weight of 1000 to 100,000 and a viscosity of 200 to 43,000 mPa.s at 100 ° C, a polymethacrylate with a viscosity of 1000 mPa.s at 100 ° C, a non-water-soluble polyglycol with a viscosity of 5 to 60 mPa.s
  • lubricant according to the invention and lubricant concentrate preferably contains a sulfur carrier, particularly a thiazole, at least one metal dialkyldithiocarbamate and / or a metal dialkyldithiophosphate and / or a phosphorus carrier, in particular an organo phosphite, preferably a Dialkylarylphosphit, particularly didecyl or Didodecylphenylphosphit, and / or a metal dialkyldithiophosphate .
  • a sulfur carrier particularly a thiazole
  • at least one metal dialkyldithiocarbamate and / or a metal dialkyldithiophosphate and / or a phosphorus carrier in particular an organo phosphite, preferably a Dialkylarylphosphit, particularly didecyl or Didodecylphenylphosphit, and / or a metal dialkyldithiophosphate
  • the sulfur carrier is preferably present in the lubricant or lubricant concentrate in an amount of 0.5 to 10% by weight, in particular 1 to 3% by weight, while the phosphorus carrier is preferably present in an amount of 0.1 to 10 % By weight, in particular from 0.1 to 5% by weight, especially from 0.5 to 2% by weight.
  • the lubricant or lubricant concentrate according to the invention can contain conventional antioxidants, metal deactivators, detergents, dispersants, antifoams and / or viscosity index improvers as further conventional additives.
  • polyolester compounds used according to the invention with at least one quaternary carbon atom in the molecule include the following compounds:
  • the underlying mono- and dipentaerythritol has the structure: in which the hydroxyl groups are partially or completely esterified, the ester groups of which are preferably straight or branched alkyl, aralkyl or aryl groups having 6 to 18, preferably 8 to 12, carbon atoms.
  • pentaerythritol ester examples include pentaerythritol monohexyl, pentaerythritol monooctyl, pentaerythritol monononylester, pentaerythritol monodecylester, pentaerythritol monododecylester, pentaerythritol monomyristylester, pentaerythritol monohexadecylester, Pentaerythritmonostearylester, pentaerythritol monooleylester, pentaerythritol monoisostearyl- and -isopalmitinklarester; the corresponding dihexyl, dioctyl, dinonyl, didecyl, didodecyl, dimyristyl, dihexadecyl, distearyl, dioleyl, diisostearyl
  • telomeric acids are compounds with relatively high molecular weights and Long-chain, star-branched structures which can be esterified in the usual way and whose esters are valuable lubricants (commercial product Kortacid T from Akzo Chemie).
  • Mineral oils which can be used according to the invention are all the usual mineral oils, from isoparaffin oil with a viscosity of 1.0 mPa.s at 20 ° C to thin spindle oil with a viscosity of 12 mPa.s at 20 ° C to highly viscous bright stock and cylinder oil with a viscosity of 540 mPa .s at 50 ° C.
  • Ucolub N9 with a viscosity of 5.7 mPa.s at 100 ° C
  • Ucolub N36A with a viscosity of 18 mPa.s at 100 ° C
  • Ucolub N 120A with a viscosity of 55 MPa.s at 100 ° C (all non-water-soluble polyglycols) from Union Carbide
  • Isopar J from Esso (an isoparaffin oil) with a viscosity at 20 ° C of 1.0 mPa.s.
  • organophosphorus compounds which can be used as phosphorus supports according to the invention are compounds of the formula in which R in each case denotes a straight-chain, branched or cyclic alkyl group having 6 to 12 carbon atoms or phenyl group substituted in the o- or p-position by a lower alkyl radical having 1 to 6 carbon atoms.
  • organophosphorus compounds of the above formula are monodecyl diphenyl phosphite, didecylphenyl phosphite, Triphenyl phosphite, dioctyl phenyl phosphite, dihexyl phenyl phosphite, diisodecyl phenyl phosphite, diisooctyl phenyl phosphite, didecyl o-methylphenyl phosphite and didecyl p-methylphenyl phosphite.
  • the metal dialkyldithiocarbamates which can be used according to the invention as sulfur carriers are compounds of the formula wherein Me is a metal from the group copper, silver, zinc, cadmium, boron, titanium, zirconium, tin, lead, vanadium, tantalum, antimony, chromium, molybdenum, tungsten, manganese, cobalt and nickel, preferably boron, nickel, cobalt or molybdenum , means.
  • the metal dialkyldithiophosphates which can be used according to the invention both as a sulfur carrier and as a phosphorus carrier are compounds of the formula wherein Me for a metal from the group copper, silver, zinc, cadmium, boron, titanium, zirconium, tin, lead, vanadium, tantalum, antimony, chromium, molybdenum, tungsten, manganese, cobalt and nickel, preferably for zinc, nickel, Titanium, vanadium, molybdenum, tungsten and manganese.
  • the alkyl group in the above-mentioned metal dialkyldithiocarbamates and metal dialkyldithiophosphates each preferably contain 4 to 8 carbon atoms, so that the metal salts mentioned are still soluble in the commercially available base oils.
  • particularly advantageous alkyl groups include the n-, i- and tert-butyl group, the n- and i-amyl group, the n- and i-hexyl group, the n- and i-heptyl group and the 2-ethylhexyl group.
  • the i-butyl group, the n- and i-amyl group and the 2-ethylhexyl group are very particularly preferred.
  • metal dialkyldithiocarbamates which can be used according to the invention with particular advantage are the following: copper dialkyldithiocarbamates and copper bisdialkyldithiocarbamates; Silver dialkyldithiocarbamates; Zinc and cadmium bisdialkyldithiocarbamates; Boron trisdialkyldithiocarbamate; Titanium, zirconium, tin and lead tetrakisdialkyldithiocarbamates and tin and lead bisdialkyldithiocarbamates; Antimony, vanadium and tantalum dialkyldithiocarbamates, tetrakis and pentakis dialkyldithiocarbamates and the dialkyldithiocarbamates in which these metals are present in mixed oxidation states; Chromium, chromium tris, chromium tetrakis and chromium hexakisdialkyldithiocarbamates
  • Particularly preferred among these compounds are the boron trisdialkyldithiocarbamates, the nickeltrisdialkyldithiocarbamates and the molybdenum tetrakis and molybdenum oxytetrakisdialkyldithiocarbamates.
  • Metal dialkyldithiophosphates which can be used with particular advantage according to the invention are the dialkyldithiophosphates of the same metals in the same oxidation states as those above for the metal dialkyldithiocarbamates have been enumerated.
  • Zinc bisdialkyldithiophosphates, nickel bis- and tris dialkyldithiophosphates, titanium and vanadium tetrakis dialkyldithiophosphates, molybdenum and tungsten tetrakis dialkyldithiophosphates and molybdenum and tungsten oxytetrakis dialkyldithiophosphates are very particularly advantageous.
  • Particularly preferred representatives of the metal dialkyldithiocarbamates used according to the invention are: Bortrisdiisobutyldithiocarbamat, Bortrisdiamyldithiocarbamat, Bortrisdi-2-ethylhexyldithiocarbamat, Nickeltrisdiisobutyldithiocarbamat, Nickeltrisdiamyldithiocarbamat, Nickeltrisdi-2-ethylhexyldithiocarbamat, Molybdäntetrakisdi-2-ethylhexyldithiocarbamat, Molybdänoxytetrakisdi-2-ethylhexyldithiocarbamat and Kobaltbisdiisobutyldithiocarbamat.
  • metal dialkyldithiophosphates used in accordance with the invention are zinc bisdi-2-ethylhexyldithiophosphate, nickel bis- and trisdi-2-ethylhexyldithiophosphate, titanium and vanadium tetrakisdi-2-ethylhexyldithiophosphate as well as molybdenum and tungsten tetrakis and molybdenum oxyethyldithiophosphate.

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

Claims (9)

  1. Un lubrifiant ou concentré de lubrifiant a base d'une huile minérale et/ou synthétique contenant au moins un composé comportant au moins un atome de carbone quaternaire et au moins une liaison esterique dans la molécule et autres additives usuels,
    characterisé en'ce qu'il contient
    a) au moins un alcool tetravalent à octavalent comportant au moins un atome de carbone quaternaire et au moins une liaison esterique dans la molécule, ayant une densité d₂₀ d'au moins 0,900 et une enthalpie ΔH d'au moins 350 kcal/kg, choisi parmi le groupe des mono-, di- et tripentaerythritoles, dont les groupes hydroxyles alcooliques sont esterifiés ou ethoxyesterifiés par un groupe alkyle, aralkyle ou aryle ramifié ou non-ramifié et comportant de 6 à 18 atomes de carbone,
    b) une composante additionelle comportant au moins un groupe hydroxyle libre dans la molécule,
    c) au moins un dialkyldithiocarbamate de métal ayant la formule générale
    Figure imgb0010
    dans laquelle
    Me   représente un métal choisi parmi le groupe de cuivre, argent, zinc, cadmium, bore, titane, zirconium, étain, plomb, vanadium, tantale, antimoine, chrome, molybdène, tungstène, manganèse, cobalt et nickel et
    Alkyl représente un groupe alkyle comportant de 4 à 8 atomes de carbone,
    d) au moins un dialkylaryl-, monoalkyldiaryl-, trialkyl- ou triarylphosphite, dont le groupe alkyle est non-ramifié, ramifié ou cyclique et comporte de 8 à 12 atomes de carbone et dont le groupe aryle est un groupe phenyle substitué en o- ou p-position par alkyle ayant de 1 à 6 atomes de carbone,
    e) un thiazole et
    f) comme autres additives usuels des agents antioxidants, des desactivateurs de métal, des détergents, des agents dispersants, des agents antimousses et/ou des agents améliorants la viscosité, connus en soi.
  2. Le lubrifiant ou concentré de lubrifiant selon la revendication 1, characterisé en ce qu'il contient comme une composante additionelle
    (g) au moins un dialkyldithiophosphate de métal ayant la formule generale
    Figure imgb0011
    dans laquelle
    Me   représente un métal choisi parmi le groupe de cuivre, argent, zinc, cadmium, bore, titane, zirconium, étain, plomb, vanadium, tantale, antimoine, chrome, molybdène, tungstène, manganèse, cobalt et nickel et
    Alkyl représente un groupe alkyle comportant de 4 à 8 atomes de carbone.
  3. Le lubrifiant ou concentre de lubrifiant selon la revendication 1 ou 2, characterise en ce qu'il contient au moins un dialkyldithiocarbamate de bore, nickel, cobalt et molybdène et/ou au moins un dialkyldithiophosphate de zinc, nickel, molybdène, tungstène, titane, vanadium et manganèse.
  4. Le lubrifiant ou concentre de lubrifiant selon la revendication 3, characterise en ce qu'il contient le diisobutyl-dithiocarbamate de bore et/ou le tris-di-2-ethylhexyldithiocarbamate de bore en combinaison avec le tris-diisobutyl-dithiocarbamate de nickel, le tris-diamyl-dithiocarbamate de nickel et/ou le tris-di-2-ethylhexyl-dithiocarbamate de nickel ainsi le bis-di-2-ethylhexyl-dithiophosphate de zinc, le tris-di-2-ethylhexyl-dithiophosphate de nickel, le tetrakis-di-2-ethylhexyl- dithiophosphate de titane, le tetrakis-di-2-ethylhexyl-dithiophosphate de vanadium, le tetrakis- ou oxytetrakis-di-2-ethylhexyldithiophosphate de molybdène, le tetrakis- et/ou oxytetrakis-di-2-ethylhexyl-dithiophosphate de tungstène.
  5. Le lubrifiant ou concentré de lubrifiant selon l'une des revendications 1 à 3, characterisé en ce qu'il contient la composante (a) en une quantité de 0,1 à 40 % en poids, préférablement de 0,1 à 20 % en poids, en particulier de 1 à 12 % en poids, spécialement de 2 à 6 % en poids, par rapport au poids de l'huile minérale et/ou synthetique.
  6. Le lubrifiant ou concentré de lubrifiant selon l'une des revendications 1 à 5, characterisé en ce qu'il contient comme huile de base une huile de navette, une huile naturelle et/ou une huile synthétique ayant une viscosité de 1,0 à 2.10⁶ mPa.s à 20°C.
  7. Le lubrifiant ou concentré de lubrifiant selon la revendications 6, characterisé en ce qu'il contient comme huile naturelle une huile minérale ayant une viscosité de 1,0 mPa.s à 20°C à 540 mPa.s à 50°C et/ou comme huile synthétique un ester d'un acide aromatique ou aliphatique, en particulier un ester d'un acide poly-α-olefin-dicarboxylique, spécialement le butylester, ayant un poids moléculaire de 1000 à 3000, préférablement le diisodecylester de l'acide phtalique, le didecylester de l'acide trimethyladipinique et le dioctylester de l'acide sébacique, un polyisobutylène ayant un poids moléculaire de 1000 à 100 000 et une viscosité de 200 à 43 000 mPa.s à 100°C, un polymethacrylate ayant une viscosité de 1000 mPa.s a 100°C, un polyglycol non-soluble dans l'eau ayant une viscosité de 5 à 60 mPa.s à 100°C, une huile isoparaffinique et/ou un alkylbenzène ayant un point d'inflammation de plus de 50°C et une viscosité de 1,0 mPa.s à 20°C à 2 000 000 mPa.s à 20°C.
  8. Le lubrifiant ou concentré de lubrifiant selon l'une des revendications 1 à 7, characterisé en ce qu'il contient le(les) composè(s) comportant du soufre en une quantité de 0,5 à 10 % en poids, préférablement de 1 à 3 % en poids.
  9. Le lubrifiant ou concentré de lubrifiant selon l'une des revendications 1 à 8, characterisé en ce qu'il contient le(les) composè(s) comportant du phosphore en une quantité de 0,1 à 5 % en poids, préferéblement de 0,5 à 2 % en poids.
EP88105725A 1987-04-10 1988-04-11 Lubrifiant ou concentré de lubrifiant Expired - Lifetime EP0286139B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19873712133 DE3712133A1 (de) 1987-04-10 1987-04-10 Schmiermittel bzw. schmiermittelkonzentrat
DE3712133 1987-04-10

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EP0286139A1 EP0286139A1 (fr) 1988-10-12
EP0286139B1 true EP0286139B1 (fr) 1994-09-07

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EP (1) EP0286139B1 (fr)
JP (1) JP2843584B2 (fr)
KR (1) KR960014936B1 (fr)
AT (1) ATE111149T1 (fr)
CA (1) CA1340272C (fr)
DE (2) DE3712133A1 (fr)
ES (1) ES2064326T3 (fr)
WO (1) WO1988008021A1 (fr)

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Publication number Priority date Publication date Assignee Title
DE3714260A1 (de) * 1987-04-29 1988-11-10 Spiess C F & Sohn Bor-tris-(dialkyl-dithiocarbamate) und verfahren zu ihrer herstellung
US4832867A (en) * 1987-10-22 1989-05-23 Idemitsu Kosan Co., Ltd. Lubricating oil composition
GB2241707A (en) * 1990-03-07 1991-09-11 Exxon Research Engineering Co Lubricating grease composition
DE4128646A1 (de) * 1991-08-29 1993-03-04 Henkel Kgaa Estermischungen von stark verzweigten carbonsaeuren
DE4128647A1 (de) * 1991-08-29 1993-03-11 Henkel Kgaa Verwendung von isopalmitinsaeureestern als schmiermittel fuer zweitaktmotoren
FR2684108B1 (fr) * 1991-11-27 1994-10-28 Mobil Oil France Nouvelle graisse destinee notamment a etre utilisee dans des joints homocinetiques.
JP4098513B2 (ja) * 2001-02-02 2008-06-11 新日本石油株式会社 潤滑油組成物
JP4801574B2 (ja) * 2006-12-11 2011-10-26 株式会社リコー 像担持体用保護剤、及び保護層形成装置、並びに画像形成方法、画像形成装置、及びプロセスカートリッジ
JP2008297501A (ja) * 2007-06-01 2008-12-11 New Japan Chem Co Ltd 軸受用潤滑油

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Publication number Priority date Publication date Assignee Title
FR1543830A (fr) * 1966-11-10 1968-10-25 Mobil Oil Corp Compositions lubrifiantes contenant des additifs anti-corrosion perfectionnés
GB1301003A (en) * 1969-07-10 1972-12-29 Ethyl Corp Lubricant materials
JPS5328862B2 (fr) * 1972-04-18 1978-08-17
US3843542A (en) * 1972-07-31 1974-10-22 Chevron Res Hydraulic oil
IT1010487B (it) * 1974-05-08 1977-01-10 Snam Progetti Esteri come componenti di lubrifi canti
US3896050A (en) * 1974-07-05 1975-07-22 Texaco Inc Lubricating oil additives
US4097388A (en) * 1976-10-12 1978-06-27 The United States Of America As Represented By The Secretary Of The Air Force Linear fluorinated polyether lubricant compositions containing perfluoroalkylether substituted phosphines
JPS59133297A (ja) * 1983-01-20 1984-07-31 Idemitsu Kosan Co Ltd 高温用潤滑油組成物
GB8422562D0 (en) * 1984-09-06 1984-10-10 Exxon Research Engineering Co Hot forming lubricant compositions
IT1188166B (it) * 1985-04-24 1988-01-07 Montefluos Spa Stabilizzanti a struttura arilfosfinica per olii e grassi perfluoropolieterei
JPS6210193A (ja) * 1985-07-08 1987-01-19 Nippon Oil Co Ltd トラクシヨンドライブ用流体組成物
DE3682715D1 (de) * 1985-07-08 1992-01-16 Nippon Oil Co Ltd Schmiermittelzusammensetzungen.

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WO1988008021A1 (fr) 1988-10-20
ES2064326T3 (es) 1995-02-01
JP2843584B2 (ja) 1999-01-06
DE3851355D1 (de) 1994-10-13
EP0286139A1 (fr) 1988-10-12
CA1340272C (fr) 1998-12-15
DE3712133C2 (fr) 1993-07-15
ATE111149T1 (de) 1994-09-15
KR960014936B1 (ko) 1996-10-21
DE3712133A1 (de) 1988-10-20
JPH01503543A (ja) 1989-11-30
KR890701717A (ko) 1989-12-21

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