EP0719314B1 - Lubricant composition containing antiwear additive combination - Google Patents

Lubricant composition containing antiwear additive combination Download PDF

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Publication number
EP0719314B1
EP0719314B1 EP94926291A EP94926291A EP0719314B1 EP 0719314 B1 EP0719314 B1 EP 0719314B1 EP 94926291 A EP94926291 A EP 94926291A EP 94926291 A EP94926291 A EP 94926291A EP 0719314 B1 EP0719314 B1 EP 0719314B1
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Prior art keywords
lubricant composition
organo
phosphorus
molybdenum
compound
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EP94926291A
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German (de)
English (en)
French (fr)
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EP0719314A1 (en
Inventor
David Gary Lawton Holt
Patrick Desmond Fraser Vernon
John Ian Atherton
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ExxonMobil Technology and Engineering Co
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Exxon Research and Engineering Co
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Priority claimed from GB939318896A external-priority patent/GB9318896D0/en
Priority claimed from GB939318895A external-priority patent/GB9318895D0/en
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M163/00Lubricating compositions characterised by the additive being a mixture of a compound of unknown or incompletely defined constitution and a non-macromolecular compound, 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
    • 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
    • C10M129/26Carboxylic acids; Salts thereof
    • C10M129/28Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M129/38Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms
    • C10M129/40Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms monocarboxylic
    • 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
    • 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
    • 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
    • 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
    • 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
    • C10M159/00Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
    • C10M159/12Reaction products
    • C10M159/18Complexes with metals
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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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/09Metal enolates, i.e. keto-enol metal complexes
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • C10M2207/126Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids monocarboxylic
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/129Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more 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
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/16Naphthenic acids
    • 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
    • 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
    • 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
    • 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
    • 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
    • C10M2223/047Thioderivatives not containing metallic elements
    • 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
    • C10M2227/00Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
    • C10M2227/09Complexes with metals
    • 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
    • C10N2070/00Specific manufacturing methods for lubricant compositions
    • C10N2070/02Concentrating of additives

Definitions

  • This invention relates to a lubricant composition containing a combination of additives providing antiwear properties, and to the antiwear additive combination contained therein.
  • an antiwear additive in lubricating oils such as engine oils. Wear results mainly from the rubbing together of two metal surfaces, i.e. in boundary lubrication regimes, such as is found in valve trains in internal combustion engines. It is believed that the antiwear additive acts to provide a protective film over the metal surfaces.
  • One well-known class of antiwear additives is the metal alkylphosphate, especially zinc dialkyldithiophosphate ("ZDDP").
  • ZDDP is employed at treat levels of 1 to 2 wt.% based on the total weight of the lubricant, which gives a phosphorus level in the lubricant typically in the range of from 0.05 to 0.15 wt.%, and a zinc level of from 0.1 to 0.2 wt.%.
  • Sulphur-containing organic phosphorus compounds are known to be used as "extreme pressure compounds" in heavy duty applications such as greases for constant velocity joints. It is also known to use sulphur-containing organic compounds of heavy metals such as molybdenum, tungsten and lead in such applications.
  • GB-A-2255346 describes an additive for grease used in constant velocity joints comprising in combination molybdenum sulphide dialkyldithiocarbamate, zinc dithiophosphate, a sulphur-phosphorus series extreme pressure compound, and lead dialkyldithiocarbamate. It is stated that the presence of the lead compound is essential to achieve the desired performance.
  • US-A-4648985 describes a lead-free extreme pressure additive, generally for lubricants based on asphalt, utilising an organic phosphate in combination with copper or molybdenum compounds selected from carboxylate, phosphate, thiophosphate and thiocarbamate, optionally with a metal-free thiocarbamate or in combination with a metal thiocarbamate (numerous metals being described).
  • the preferred metals are copper and zinc.
  • EP-A-0516461 describes a dispersant additive for lubricating oils showing improved compatibility with elastomeric seal material which comprises in combination a metal dihydrocarbyl dithiocarbamate or dithiocarbamate and a phosphorylated ashless dispersant.
  • Various metal compounds are described including molybdenum dithiophosphate.
  • EP-A-0316610 describes a multipurpose antiwear, antiseizure and corrosion inhibiting additive for lubricating oils utilising a combination of an organo-phosphorus compound selected from various phosphines and phosphites and an organo-molybdenum compound selected from oxysulphide alkylphosphorodithioates and oxysulphide alkyl dithiocarbamates.
  • GB-A-1373588 describes an antiwear, antioxidant additive combination comprising a metal dialkyldithiocarbamate and/or a metal alkyl, aryl or aralkyl dithiophosphate and a metal-free phosphorus compound selected from sulphurised sperm oil esterified with dithiophosphate, sulphurised terpene esterified with dithiophosphate, sulphurised and phosphated sperm oil and phosphorus polysulphide. Many metals are mentioned including molybdenum, zinc and lead.
  • EP-A-566326 is an earlier European application having a filing date of 8 April 1993 and a publication date of 20 October 1993. Accordingly it is part of the state of the art for the present invention for novelty only and only in respect of the following Contracting States: BE, DE, ES, FR, GB, IT, LU, NL, SE. It describes a lubricant composition, specifically a lubricant grease for reducing shudder in inboard constant velocity joints.
  • the grease comprises a base oil, a thickener, an organic molybdenum compound selected from molybdenum dithiocarbamate and molybdenum dithiophosphate, and an ashless additive selected from ashless dithiophosphates and ashless dithiocarbamates.
  • the present invention provides a lubricant composition
  • compounds (a), (b) when used in combination with reduced levels of a selected zinc thiophosphate act synergistically to provide better wear protection than that achieved using a comparable amount (i.e. an amount providing a similar total level of phosphorus) of the zinc thiophosphate alone.
  • the combination includes, in addition to (a) and (b), a zinc thiophosphate compound (c) selected from one or more of zinc dialkyldithiophosphate, zinc diaryldithiophosphate, zinc alkylaryldithiophosphate and zinc arylalkyldithiophosphate.
  • a zinc thiophosphate compound (c) selected from one or more of zinc dialkyldithiophosphate, zinc diaryldithiophosphate, zinc alkylaryldithiophosphate and zinc arylalkyldithiophosphate.
  • organo-molybdenum compound can replace some of the zinc thiophosphate compound used in lubricant compositions with the effect that the phosphorus level in the lubricant is reduced without substantially reducing, indeed increasing the antiwear performance of the lubricant.
  • the organo-molybdenum compound may comprise a molybdenum carbamate, preferably a dicarbamate and more preferably a dithiocarbamate (MoDTC) the organo group(s) of which may be substituted with a hydrocarbyl groups and/or one or more hetero atoms, with the proviso that the organo group selected results in an organo-molybdenum compound that is oil-soluble or oil-dispersible, preferably oil-soluble.
  • MoDTC dithiocarbamate
  • MoDTC decomposes when heated in use to decomposition products which include free amine and carbon disulphide. Both such products are aggressive towards copper which is present in the engine bearings. Wear in bearings is particularly objectionable since repair involves complete dismantling of the engine. Carbon disulphide tends to boil off fairly rapidly and does not constitute a special problem. However even small amounts of free amine can cause damage.
  • synergisms described above extend not only to carbamates of molybdenum but also to molybdenum compounds which are nitrogen free and which therefore do not decompose to free amine.
  • a preferred organo-molybdenum compound is also free from sulphur.
  • the organo-molybdenum compound is nitrogen-free. It is preferably selected from a carboxylate and a xanthate or mixtures thereof the organo group(s) of which may be substituted with a hydrocarbyl group, again with the proviso that the organo group selected results in an organo-molybdenum compound that is oil-soluble or oil-dispersible, preferably oil-soluble.
  • the preferred organo-molybdenum compound comprises a carboxylate. Not only do such compounds contain no nitrogen or phosphorus but they are relatively cheap and contain a higher proportion of molybdenum than the more complex compounds. As will be described in more detail, it is believed that the effective additive content is governed by the metal content. Thus only about one third of the amount e.g. of molybdenum 2-ethyl hexanoate need be used by comparison with molybdenum dithiocarbamate.
  • the present invention provides an antiwear agent comprising a combination of (a) an organo-molybdenum compound as above described, (b) an ashless organo-phosphorus compound as above described and, optionally, (c) a zinc thiophosphate as above described.
  • the present invention provides the use in a lubricant composition of the combination of (a) an organo-molybdenum compound as above described, (b) an ashless organo-phosphorus compound as above described and, optionally, (c) a zinc thiophosphate as above described, as an antiwear agent.
  • the invention provides an additive concentrate comprising in combination: (a) an organo-molybdenum compound as above described, (b) an ashless organo-phosphorus compound as above described, optionally (c) a zinc thiophosphate as above described and a carrier fluid.
  • the organo-molybdenum compound is preferably a molybdenum dithiocarbamate of the formula : where R 1 , R 2 , R 3 and R 4 each independently represent a hydrogen atom, a C 1 to C 20 alkyl group, a C 6 to C 20 cycloalkyl, aryl, alkylaryl or aralkyl group, or a C 3 to C 20 hydrocarbyl group containing an ester, ether, alcohol or carboxyl group; and X 1 X 2 , Y 1 and Y 2 each independently represent a sulphur or oxygen atom.
  • R 1 , R 2 , R 3 and R 4 examples include 2-ethylhexyl, nonylphenyl, methyl, ethyl, n-propyl, iso-propyl, n-butyl, t-butyl, n-hexyl, n-octyl, nonyl, decyl, dodecyl, tridecyl, lauryl, oleyl, linoleyl, cyclohexyl and phenylmethyl.
  • R 1 to R 4 are each C 6 to C 18 alkyl groups, more preferably C 10 to C 14 .
  • X 1 and X 2 are the same, and Y 1 and Y 2 are the same. Most preferably X 1 and X 2 are both sulphur atoms. and Y 1 and Y 2 are both oxygen atoms.
  • the organo-molybdenum compound is sulphurised oxymolybdenum dithiocarbamate wherein the thiocarbamate groups contain C 10 to C 14 alkyl groups.
  • Such compounds are commercially available and are supplied, for example, by R.T. Vanderbilt Company.
  • organo group of the organo-molybdenum compound is a carboxylate
  • this is preferably a C 1 to C 50 , more preferably a C 6 to C 18 , carboxylate group.
  • suitable carboxylates include octoate, e.g. 2-ethyl hexanoate, naphthenate and stearate. These compounds may be prepared, for example, by reacting molybdenum trioxide with the alkali metal salt of the appropriate carboxylic acid under suitable conditions.
  • the organo group of the organo-molybdenum compound is a xanthate
  • the compound preferably has the formula : Mo 2 (ROCS 2 ) 4 where R is a C 1 to C 30 hydrocarbyl group, preferably an alkyl group.
  • R is a C 1 to C 30 hydrocarbyl group, preferably an alkyl group.
  • the ashless organo-phosphorus compound is selected from a phosphorothiolothionate, a phosphorothionate and mixtures thereof.
  • Phosphorothiolothionates have the general formula: where R 5 , R 6 and R 7 each independently represent a hydrocarbyl group which may be substituted with one or more functional groups or hetero atoms, or may be unsubstituted, and which may be branched or straight-chain.
  • R 5 and R 6 are each a C 1 to C 30 alkyl group, or a C 6 to C 30 cycloalkyl, aryl, aralkyl or alkylaryl group.
  • R 7 is preferably a C 1 to C 30 alkyl group, a C 6 to C 30 cycloalkyl, aryl, aralkyl or alkylaryl group, or a C 1 to C 30 hydrocarbyl group containing one or more carboxylic acid, ester, alcohol, ether or amine groups, or an ammonium ion, preferably one or more carboxylic acid groups.
  • Suitable phosphorothiolothionates which are commercially available include VANLUBE 727, VANLUBE 7611 both supplied by R.T. Vanderbilt Company, IRGALUBE 63 supplied by Ciba-Geigy, and ECA 6330 supplied by Exxon Chemical Company.
  • Phosphorothionates have the general formula: where R 8 , R 9 , and R 10 each represent a hydrocarbyl group which may be substituted with one or more functional groups or hetero atoms, or may be unsubstituted, and which may be branched or straight-chain.
  • R 8 and R 9 are each a C 1 to C 30 alkyl group or a C 6 to C 30 cycloalkyl, aryl, aralkyl or alkylaryl group.
  • R 10 is preferably a C 1 to C 30 alkyl group or a C 6 to C 30 cycloalkyl, aryl, aralkyl or alkylaryl group, or a C 1 to C 30 hydrocarbyl group containing one or more amine, carboxylic acid, ester, alcohol or ether groups, or an ammonium ion, preferably an amine group or ammonium ion.
  • Suitable phosphorothionates which are commercially available include IRGALUBE TPPT supplied by Ciba-Geigy. Phosphorus thionates may also be obtained from the reaction of amines with dialkyldithiophosphoric acids.
  • the zinc thiophosphate compound (c) has the general formula : where R 11 , R 12 , R 13 and R 14 each independently represent a hydrogen atom, a C 1 to C 20 alkyl group, a C 6 to C 26 cycloalkyl, aryl, alkylaryl or aralkyl group, or a C 3 to C 20 hydrocarbyl group containing an ester, ether, alcohol or carboxyl group.
  • each of R 11 to R 14 is a C 2 to C 18 , more preferably C 3 to C 8 , alkyl group which may be straight-chain or branched.
  • Such compounds are commercially available and are supplied by, for example, Exxon Chemical Company.
  • each of the antiwear additives (a) and (b) to be included in the lubricant composition according to the invention are the amounts that are effective in providing the desired level of antiwear performance, whilst reducing the amount of phosphorus to an acceptable level.
  • the antiwear properties of the organo-molybdenum compound (a) are generally attributable to the presence of the molybdenum.
  • the amount of molybdenum contained in the lubricant composition is from 0.001 to 0.5 wt.%, more preferably 0.005 to 0.2 wt.%, and most preferably 0.01 to 0.05 wt.%, based on the total weight of the lubricant composition.
  • the amount of organo-molybdenum compound that this corresponds to depends upon the type of compound selected.
  • the amount of compound used depends on the molecular weight of the R groups contained in the thiocarbamate groups, as defined in formula (I) above. Typically, however, the amount of molybdenum dithiocarbamate used is preferably from 0.01 to 3.0 wt.%, more preferably from 0.02 to 2.0 wt.%, and most preferably from 0.05 to 1.0 wt.%, based on the total weight of the lubricant composition.
  • the amount of compound used depends upon the molecular weight of the carboxylate group selected.
  • the amount of molybdenum carboxylate used is preferably from 0.005 to 2.5 wt.%, more preferably from 0.025 to 1.0 wt.%, and most preferably from 0.05 to 0.25 wt.%, based on the total weight of the lubricant composition.
  • the amount of compound used depends upon the molecular weight of the hydrocarbyl, e.g. alkyl, groups contained in the xanthate groups. Typically, however, the amount of molybdenum xanthate used is preferably from 0.003 to 2.0 wt.%, more preferably from 0.01 to 0.7 wt.% and most preferably from 0.03 to 0.2 wt.%, based on the total weight of the lubricant composition.
  • the antiwear properties of the ashless organo-phosphorus compound (b) and the zinc thiophosphate, when used, are generally attributable to the presence of the phosphorus.
  • the total amount of phosphorus contained in the lubricant composition is from 0.001 to 0.3 wt.%, more preferably from 0.01 to 0.2 wt.%, and most preferably from 0.02 to 0.1 wt.%, based on the total weight of the lubricant composition.
  • the amount of ashless organo-phosphorus compound and zinc thiophosphate compound (when used) that this corresponds to depends on the relative proportions of these compounds and the molecular weights of the particular compounds selected.
  • the amount of ashless organo-phosphorus compound incorporated into the lubricant composition is preferably from 0.01 to 3.0 wt.%, more preferably from 0.1 to 2.0 wt.%, and most preferably from 0.2 to 1.0 wt.%, based on the total weight of the lubricant composition
  • the amount of zinc thiophosphate compound is preferably from 0.01 to 3.0 wt, more preferably 0.1 to 2.0 wt.%, and most preferably 0.2 to 1.0 wt.% based on the total weight of the lubricant composition.
  • the ratio of organo-molybdenum compound (a) to ashless organo-phosphorus compound (b) is preferably such that the weight ratio of molybdenum to phosphorus in the lubricant composition, due to the presence of compounds (a) and (b), is from 1:50 to 100:1, more preferably from 1:10 to 20:1, and most preferably from 1:1 to 10:1.
  • the weight ratio of phosphorus derived from the ashless organo-phosphorus compound (b) to zinc thiophosphate compound (c) (when used) is preferably from 10:1 to 1:20, more preferably from 5:1 to 1:15 and most preferably 1:1 to 1:10.
  • the base oil employed in the lubricant composition according to the invention may be any base oil having a viscosity suitable for use of the lubricant in an engine e.g. as a crankcase oil or gear oil.
  • the base oil may be, for example, a conventionally refined mineral oil, an oil derived from coal tar or shale, a vegetable oil, an animal oil, a hydrocracked oil, or a synthetic oil, or a mixture of two or more of these types of oils.
  • synthetic oils include hydroisomerised paraffins, polyalphaolefins, polybutene, alkylbenzenes, polyglycols, esters such as polyol esters or dibasic carboxylic acid esters, alkylene oxide polymers, and silicone oils.
  • the viscosity of the base oil depends upon the intended use, but generally is in the range of from 3 to 26 cSt (mm 2 /s)at 100°C, preferably from 3 to 20 cSt (mm 2 /s)at 100°C.
  • the antiwear additive compounds (a) and (b), and (c) when used, may be mixed directly with the base oil, but, for ease of handling and introduction of the compounds to the base oil, are preferably in the form of additive concentrate comprising the additive compound, or mixture of both compounds, contained in a carrier fluid.
  • the carrier fluid is typically an oil and may be, for example, any of the oils mentioned above in the description of the base oil. Alternatively, it may be an organic solvent, for example naphtha, benzene, toluene, xylene and the like.
  • the carrier fluid should be compatible with the base oil of the lubricant composition, but otherwise is preferably inert.
  • the concentrate will comprise from 10 to 90 wt.% of the additive(s), preferably from 30 to 70 wt.%, the balance being the carrier fluid.
  • the lubricant composition according to the invention may also contain other additives, which may be added directly to the base oil, as a separate additive concentrate, or included in the concentrate of the antiwear additives.
  • other additives that may be incorporated include one or more of a detergent, dispersant, antioxidant, corrosion inhibitor, extreme pressure agent. antifoaming agent, pour point depressant and viscosity index improver.
  • Such additives are well-known and the selection of appropriate additives could readily be determined by a person skilled in the art of lubricant formulating.
  • the lubricant composition may find use in any application where the parts to be lubricated are subject to wear. It is especially suitable for use as an engine oil for internal combustion engines.
  • a number of engine oils were formulated by blending an organo-molybdenum compound and an ashless organo-phosphorus compound with a conventional engine oil formulation (the "basecase” oil) which was based on a conventionally refined mineral oil and contained standard engine oil additives except that ZDDP was omitted.
  • basecase oil a conventional engine oil formulation
  • further engine oils were formulated omitting one or more of the antiwear additives, and, in one example, ZDDP was added.
  • the organo-molybdenum compounds used were: (i) MOLYVAN 822 (trade name) a molybdenum dithiocarbamate supplied by R.T. Vanderbilt Company, (ii) MOLYNAPALL (trade name), a molybdenum naphthenate supplied by Mooney Chemicals, and (iii) MOLYHEXCEM (trade name), molybdenum 2-ethyl hexanoate supplied by Mooney Chemicals.
  • the molybdenum content of each of these compounds was determined using ICP (inductively-coupled plasma) analysis.
  • the ashless organo-phosphorus compounds used were: (i) IRGALUBE TPPT (trade name), a phosphorothionate supplied by Ciba-Geigy, (ii) VANLUBE 727 (trade name), a phosphorothiolothionate supplied by R.T. Vanderbilt Company, and (iii) "Amine DDP", an amine derivative of a phosphorothionate obtained by reacting the amine PRIMENE JMT (trade name) supplied by Rohm and Haas with dioctyldithiophosphoric acid.
  • the phosphorus content of each of these compounds was determined using X-ray fluorescent analysis according to standard test AMS 86.002.
  • the ZDDP compound used was PARANOX 14 supplied by Exxon Chemical Company.
  • the phosphorus content of this compound was also determined using the above X-ray fluorescent analysis technique.
  • the resulting engine oils were tested for valve train wear by measuring camshaft wear and tappet scuffing using a motored cylinder head test rig which is equivalent to the industry standard TU-3 engine test CEC L-38-T-87, which test procedure is available from the CEC Secretariat, 61 New Cavendish Street, London W1 8AB.
  • An engine oil was formulated by adding the following antiwear additives to a basecase oil consisting of conventional engine oil based on a conventionally refined mineral oil and containing standard engine oil additives other than ZDDP:
  • the amount of molybdenum contained in (a) was determined using ICP (inductively-coupled plasma) analysis.
  • the amount of phosphorus contained in each of (b) and (c) was determined using X-ray fluorescent analysis according to standard test AMS 86.002.
  • Comparative engine oils were formulated using the same basecase oil and omitting one or more of the above antiwear additives (a), (b) and (c).
  • the resulting engine oils were tested for valve train wear by measuring tappet wear according to the standard industry engine test VW 5106 Cam and Tappet Rig.
  • Example Organo-Mo Ashless-P ZDDP % Mo % P %Total active ingredient Max. Tappet wear ( ⁇ m) 4A 0.2% 0.8% 1.0% 0.01 0.10 0.11 100 4B - - 1.2% - 0.10 0.10 123 4C 0.2% - 1.0% 0.01 0.09 0.10 127 4D - 0.8% 1.0% - 0.10 0.10 123

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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)
  • Lubricants (AREA)
EP94926291A 1993-09-13 1994-09-09 Lubricant composition containing antiwear additive combination Expired - Lifetime EP0719314B1 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
GB9318895 1993-09-13
GB939318896A GB9318896D0 (en) 1993-09-13 1993-09-13 Lubricant composition containing antiwear additive combination
GB9318896 1993-09-13
GB939318895A GB9318895D0 (en) 1993-09-13 1993-09-13 Lubricant composition containing antiwear additive combination
PCT/GB1994/001971 WO1995007964A1 (en) 1993-09-13 1994-09-09 Lubricant composition containing antiwear additive combination

Publications (2)

Publication Number Publication Date
EP0719314A1 EP0719314A1 (en) 1996-07-03
EP0719314B1 true EP0719314B1 (en) 1999-01-07

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EP94926291A Expired - Lifetime EP0719314B1 (en) 1993-09-13 1994-09-09 Lubricant composition containing antiwear additive combination

Country Status (11)

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EP (1) EP0719314B1 (ko)
JP (1) JPH09506910A (ko)
KR (1) KR100237074B1 (ko)
AT (1) ATE175438T1 (ko)
CA (1) CA2171538C (ko)
DE (1) DE69415817T2 (ko)
ES (1) ES2128581T3 (ko)
HK (1) HK1014024A1 (ko)
MY (1) MY116337A (ko)
SG (1) SG47398A1 (ko)
WO (1) WO1995007964A1 (ko)

Cited By (1)

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Publication number Priority date Publication date Assignee Title
DE112011103822T5 (de) 2010-11-19 2013-08-22 Chevron U.S.A. Inc. Schmiermittel für Schlagwerkausrüstung

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EP0903399B1 (de) * 1997-09-18 2007-02-14 Ciba SC Holding AG Schmierstoffzusammensetzungen mit Thiophosphorsäureestern und Dithiophosphorsäureestern
US5939364A (en) * 1997-12-12 1999-08-17 Exxon Research & Engineering Co. Lubricating oil containing additive comprising reaction product of molybdenum dithiocarbamate and dihydrocarbyl dithiophosphoric acid
KR20030090891A (ko) * 2002-05-22 2003-12-01 현대자동차주식회사 자동차 기어유 조성물
KR100488860B1 (ko) * 2002-07-25 2005-05-11 현대자동차주식회사 무단변속기유 조성물
US7884059B2 (en) 2004-10-20 2011-02-08 Afton Chemical Corporation Oil-soluble molybdenum derivatives derived from hydroxyethyl-substituted Mannich bases
CN101007977B (zh) * 2006-01-27 2011-12-21 广东高奇能源工程有限公司 用于机动车发动机的油路纳米护理剂
WO2017171020A1 (ja) * 2016-03-31 2017-10-05 出光興産株式会社 潤滑油組成物及びそれを使用した精密減速機
EP3438233B1 (en) * 2016-03-31 2022-05-04 Idemitsu Kosan Co., Ltd. Lubricating oil composition, and precision reduction gear using same
CN109652171B (zh) * 2017-10-12 2021-12-14 中国石油化工股份有限公司 一种工业机器人关节rv减速机专用油组合物
CN116515549A (zh) * 2023-04-28 2023-08-01 安徽金德润滑科技有限公司 一种长寿命风电齿轮油及其制备方法

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US4612129A (en) * 1985-01-31 1986-09-16 The Lubrizol Corporation Sulfur-containing compositions, and additive concentrates and lubricating oils containing same
US4692256A (en) * 1985-06-12 1987-09-08 Asahi Denka Kogyo K.K. Molybdenum-containing lubricant composition
US4832867A (en) * 1987-10-22 1989-05-23 Idemitsu Kosan Co., Ltd. Lubricating oil composition
GB8826961D0 (en) * 1988-11-18 1988-12-21 Castrol Ltd Lubricant compositions
IT1229656B (it) * 1989-04-21 1991-09-06 Mini Ricerca Scient Tecnolog Composizioni lubrificanti contenenti ditiofosfati non metallici.
US4966719A (en) * 1990-03-12 1990-10-30 Exxon Research & Engineering Company Multifunctional molybdenum and sulfur containing lube additives
JP2989311B2 (ja) * 1991-04-30 1999-12-13 協同油脂株式会社 等速ジョイント用グリース組成物
CA2093029C (en) * 1992-04-14 2003-07-29 Jon C. Root Lubricants, particularly lubricating grease compositions for constant velocity universal joints
JPH0680981A (ja) * 1992-08-31 1994-03-22 Tonen Corp 内燃機関用潤滑油組成物

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE112011103822T5 (de) 2010-11-19 2013-08-22 Chevron U.S.A. Inc. Schmiermittel für Schlagwerkausrüstung

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JPH09506910A (ja) 1997-07-08
DE69415817T2 (de) 1999-06-10
KR100237074B1 (ko) 2000-01-15
CA2171538C (en) 2004-10-26
ES2128581T3 (es) 1999-05-16
CA2171538A1 (en) 1995-03-23
KR960705009A (ko) 1996-10-09
DE69415817D1 (de) 1999-02-18
ATE175438T1 (de) 1999-01-15
EP0719314A1 (en) 1996-07-03
WO1995007964A1 (en) 1995-03-23
SG47398A1 (en) 1998-04-17
HK1014024A1 (en) 1999-09-17
MY116337A (en) 2004-01-31

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