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)
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
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    • 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
    • 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
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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
    • C10M2207/129Carboxylix 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
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    • 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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Abstract

A lubricant composition is described, particularly for engine oils, comprising a base oil of viscosity from 3 to 26 cSt (mm<2>/s) at 100 DEG C and an antiwear additive combination comprising (a) an oil soluble or oil dispersible phosphorus-free organo-molybdenum compound, (b) an ashless, sulphur-containing organo-phosphorus compound and optionally (c) a zinc thiophosphate compound selected from one or more of zinc dialkyldithiophosphate, zinc diaryldithiophosphate, zinc alkylaryldithiophosphate and zinc arylalkyldithiophosphate. The molybdenum compound may be a carbamate, e.g. molybdenum dithiocarbamate (MoDTC) but is preferably nitrogen-free, e.g. a carboxylate.

Description

This invention relates to a lubricant composition containing a combination of additives providing antiwear properties, and to the antiwear additive combination contained therein.
It is well-known to include 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"). Generally 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.%.
In recent years there has been increasing concern that lubricant ash levels, such as that produced by the zinc in ZDDP, contribute to particulate emissions from internal combustion engines. There is also concern that the phosphorus from the lubricant tends to poison catalysts used in catalytic converters, thereby preventing them from functioning to full effect. However, any reduction in ZDDP treat levels has the disadvantage that it will reduce the antiwear properties of the lubricant.
There is therefore a need for an effective antiwear additive with reduced zinc and phosphorus levels.
We have found that a phosphorus-free organo-molybdenum compound and an ashless sulphur-containing organo-phosphorus compound act together synergistically to provide improved antiwear performance when used in a lubricant composition. By using this combination of compounds it becomes possible to achieve the same or better performance than that achieved with ZDDP, with significantly lower levels of phosphorus.
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. Thus 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.
Organic phosphorus compounds are also used as ashless dispersants. Thus 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.
In one aspect the present invention provides a lubricant composition comprising a base oil of viscosity from 3 to 26 cSt (mm2/s) at 100°C and an antiwear additive combination comprising
  • (a) an oil soluble or oil-dispersible phosphorus-free organo-molybdenum compound wherein the organo group of the molybdenum compound is selected from carbamate, carboxylate and xanthate groups and mixtures thereof, which groups may be substituted with a hydrocarbyl group and/or one or more hetero atoms, and
  • (b) an ashless, sulphur-containing organo phosphorus compound selected from:
  • (i) a phosphorothiolothionate of the formula :
    Figure 00030001
       wherein R5, R6 and R7 are each independently an unsubstituted branched or straight chain hydrocarbyl group or a branched or straight chain hydrocarbyl group substituted with one or more functional groups or hetero atoms,
  • (ii) a phosphorothionate of the formula :
    Figure 00030002
       wherein R8, R9, and R10 are as defined for R5, R6, and R7 above; and
  • (iii) a mixture of (i) and (ii).
  • Furthermore, we have found surprisingly that 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.
    Accordingly in a preferred lubricant composition 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.
    This provides the advantage that the 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.
    However it is known that 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.
    We have found that the 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.
    Accordingly in a preferred combination of (a) and (b) together optionally with (c) 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.
    In another aspect 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.
    In a further aspect 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.
    In a yet further aspect 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.
    Where the organo group is a carbamate, the organo-molybdenum compound is preferably a molybdenum dithiocarbamate of the formula :
    Figure 00050001
    where R1, R2, R3 and R4 each independently represent a hydrogen atom, a C1 to C20 alkyl group, a C6 to C20 cycloalkyl, aryl, alkylaryl or aralkyl group, or a C3 to C20 hydrocarbyl group containing an ester, ether, alcohol or carboxyl group; and X1 X2, Y1 and Y2 each independently represent a sulphur or oxygen atom.
    Examples of suitable groups for each of R1, R2, R3 and R4 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. Preferably R1 to R4 are each C6 to C18 alkyl groups, more preferably C10 to C14.
    It is preferred that X1 and X2 are the same, and Y1 and Y2 are the same. Most preferably X1 and X2 are both sulphur atoms. and Y1 and Y2 are both oxygen atoms.
    Thus in a preferred embodiment the organo-molybdenum compound is sulphurised oxymolybdenum dithiocarbamate wherein the thiocarbamate groups contain C10 to C14 alkyl groups. Such compounds are commercially available and are supplied, for example, by R.T. Vanderbilt Company.
    Where the organo group of the organo-molybdenum compound is a carboxylate, this is preferably a C1 to C50, more preferably a C6 to C18, carboxylate group. Examples of 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.
    Where the organo group of the organo-molybdenum compound is a xanthate, the compound preferably has the formula : Mo2 (ROCS2)4 where R is a C1 to C30 hydrocarbyl group, preferably an alkyl group. Examples of suitable molybdenum xanthate compounds and their method of preparation are described in European patent application EP-A-433025, the disclosure of which is incorporated herein by reference.
    The ashless organo-phosphorus compound is selected from a phosphorothiolothionate, a phosphorothionate and mixtures thereof.
    Phosphorothiolothionates have the general formula:
    Figure 00060001
    where R5, R6 and R7 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.
    Preferably R5 and R6 are each a C1 to C30 alkyl group, or a C6 to C30 cycloalkyl, aryl, aralkyl or alkylaryl group. R7 is preferably a C1 to C30 alkyl group, a C6 to C30 cycloalkyl, aryl, aralkyl or alkylaryl group, or a C1 to C30 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. Examples of 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:
    Figure 00070001
    where R8, R9, and R10 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.
    Preferably R8 and R9 are each a C1 to C30 alkyl group or a C6 to C30 cycloalkyl, aryl, aralkyl or alkylaryl group. R10 is preferably a C1 to C30 alkyl group or a C6 to C30 cycloalkyl, aryl, aralkyl or alkylaryl group, or a C1 to C30 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. Examples of 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 :
    Figure 00070002
    where R11, R12, R13 and R14 each independently represent a hydrogen atom, a C1 to C20 alkyl group, a C6 to C26 cycloalkyl, aryl, alkylaryl or aralkyl group, or a C3 to C20 hydrocarbyl group containing an ester, ether, alcohol or carboxyl group. Preferably each of R11 to R14 is a C2 to C18, more preferably C3 to C8, alkyl group which may be straight-chain or branched. Such compounds are commercially available and are supplied by, for example, Exxon Chemical Company.
    The amounts of 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.
    Whilst not being limited to any particular theory, it is believed that the antiwear properties of the organo-molybdenum compound (a) are generally attributable to the presence of the molybdenum. Thus when determining the amount of organo-molybdenum compound to be incorporated into the lubricant composition, one first needs to determine the desired amount of molybdenum. Preferably 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.
    Where the organo-molybdenum compound is a dithiocarbamate, 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.
    Where the organo-molybdenum compound is a carboxylate, the amount of compound used depends upon the molecular weight of the carboxylate group selected. For example, where the carboxylate is 2-ethyl hexanoate, 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.
    Where the organo-molybdenum compound is a xanthate, 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.
    Similarly, it is believed that 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. Thus, when determining the amounts of these compounds to incorporate, one first needs to determine the desired amount of phosphorus in the lubricant composition. Preferably 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. Typically, however, 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, and 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. Thus 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. Examples of 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 (mm2/s)at 100°C, preferably from 3 to 20 cSt (mm2/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. Generally 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. For example, where the lubricant is an engine oil, 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.
    The invention is illustrated by the following Examples.
    Examples 1 to 3
    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. For comparative purposes, further engine oils were formulated omitting one or more of the antiwear additives, and, in one example, ZDDP was added.
    The formulations are listed in Table 1 below.
    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.
    The results are given in Table 1 below. All percentages are by weight based on the weight of the fully formulated engine oil.
    In Table 1 the following abbreviations are used:
    PN 14 =
    PARANOX 14
    MV 822 =
    MOLYVAN 822
    M.N.ALL =
    MOLYNAPALL
    M.H.CEM =
    MOLYHEXCEM
    I.TPPT =
    IRGALUBE TPPT
    VL 727 =
    VANLUBE 727
    P.JMT =
    PRIMENE JMT reacted with dioctyldithiophosphoric acid
    Good results are indicated by a low value for camshaft wear and a high value for tappet scuffing. From the results it can be seen that addition of an organo-molybdenum compound as the sole antiwear additive produces only a small improvement in camshaft wear and some improvement in tappet scuffing over the basecase oil containing no antiwear additive. Likewise addition of solely an organo-phosphorus compound produces some improvement in camshaft wear and tappet scuffing. However addition of both compounds produces significant antiwear improvement. Furthermore the improvement achieved is greater than that achieved using ZDDP, even when the total active ingredient is higher for the ZDDP-containing formulation (Example 1A) than the formulation according to the invention (Example 1D). Furthermore, better results than with ZDDP alone were achieved when the organo-molybdenum compound was 2-ethyl hexanoate (Example 3E) the results being only marginally less than with dithiocarbamate (Example 3C) and was achieved using only 0.07 wt.% of the additive compound as against 0.2 wt.% in the case of dithiocarbamate.
    Figure 00120001
    Example 4
    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:
  • (a) 0.2 wt.% MOLYVAN 822 (molybdenum dithiocarbamate as in Example 1)
  • (b) 0.8 wt.% ECA 6330, a phosphorothiolothionate supplied by Exxon Chemical Company, and
  • (c) 1.0 wt.% PARANOX 14 (ZDDP as in Example 1)
  • 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 Test (procedure P-VW 5106), which test procedure is available from VW AG, Postfach 3180, Wolfsburg 1, Germany
    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.
    The results are given in Table 2 below. All percentages are by weight based on the weight of the fully formulated engine oil.
    Example Organo-Mo Ashless-P ZDDP % Mo % P %Total active ingredient Max. Tappet wear (µm)
    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
    The lower the tappet wear value the better the antiwear performance of the lubricant. Thus the results show that for the same level of total phosphorus a significant improvement in antiwear performance is achieved when the antiwear agent is a combination of organo-molybdenum compound, ashless organo-phosphorus compound and ZDDP.

    Claims (12)

    1. An antiwear additive combination for use in a lubricant composition comprising :
      (a) an oil soluble or oil-dispersible phosphorus-free organo-molybdenum compound wherein the organo group of the molybdenum compound is selected from carbamate, carboxylate and xanthate groups and mixtures thereof, which groups may be substituted with a hydrocarbyl group and/or one or more hetero atoms, and
      (b) an ashless, sulphur-containing organo phosphorus compound selected from:
      (i) a phosphorothiolothionate of the formula :
      Figure 00180001
         wherein R5, R6 and R7 are each independently an unsubstituted branched or straight-chain hydrocarbyl group or a branched or straight-chain hydrocarbyl group substituted with one or more functional groups or hetero atoms,
      (ii) a phosphorothionate of the formula :
      Figure 00180002
         wherein R8, R9, and R10 are as defined for R5, R6, and R7 above; and
      (iii) a mixture of (i) and (ii).
    2. An additive combination according to claim 1 wherein (a) is a molybdenum dithiocarbamate of the formula :
      Figure 00190001
      where R1 R2, R3 and R4 are each independently a hydrogen atom, a C1 - C20 alkyl group, a C6 - C20 cycloalkyl, aryl, alkylaryl or arylalkyl group, or a C3 - C20 hydrocarbyl group containing an ester, ether, alcohol or carboxyl group; and
      X1, X2 Y1 and Y2 are each independently a sulphur or an oxygen atom.
    3. An additive combination according to claim 1 wherein (a) is a molybdenum carboxylate wherein the carboxylate group contains from 1 to 50 carbon atoms.
    4. An additive combination according to claim 1 wherein (a) is a molybdenum xanthate of the formula Mo2(ROCS2)4 where R is a C1 - C30 hydrocarbyl group.
    5. An additive combination according to any preceding claim wherein the combination includes in addition to (a) and (b):
      (c) a zinc thiophosphate compound selected from one or more of zinc dialkyldithiophosphate, zinc diaryldithiophosphate, zinc alkylaryldithiophosphate and zinc arylalkyldithiophosphate.
    6. An additive concentrate comprising a carrier fluid in which the components of the additive combination of any preceding claim is or are dispersed and/or dissolved.
    7. A lubricant composition comprising a base oil viscosity of from 3 to 26 (e.g., 3 to 20) cSt (mm2/s) at 100°C, and an anti-wear additive combination according to any of claims 1 to 5.
    8. A lubricant composition according to claim 7 wherein the amount of organo-molybdenum compound contained in the lubricant composition is such that the amount of molybdenum contained in the lubricant composition is from 0.001 to 0.5 wt.%, preferably 0.005 to 0.2 wt.%, based on the total weight of the lubricant composition and/or wherein the amount of ashless organo-phosphorus compound contained in the lubricant composition is such that the amount of phosphorus contained in the lubricant composition is from 0.001 to 0.3 wt.%, preferably 0.01 to 0.2 wt.%, based on the total weight of the lubricant composition.
    9. A lubricant composition according to claim 7 or 8 wherein the ratio of organo-molybdenum compound to the ashless organo-phosphorus compound in the lubricant composition is such that the weight ratio of molybdenum to phosphorus in the lubricant composition is from 1:50 to 100:1, preferably from 1:10 to 20:1.
    10. A lubricant composition according to any of claims 7 to 9 wherein the amount of zinc thiophosphate compound and ashless organo-phosphorus compound contained in the lubricant composition is such that the amount of phosphorus contained in the lubricant composition is from 0.001 to 0.3 wt.%, preferably from 0.01 to 0.2 wt.%, based on the total weight of the lubricant composition and/or wherein the ratio of organo-molybdenum compound to the ashless organo-phosphorus and zinc thiophosphate compounds in the lubricant composition is such that the weight ratio of molybdenum to phosphorus in the lubricant composition is from 1:50 to 100:1, preferably from 1:10 to 20:1.
    11. A lubricant composition according to any of claims 7 to 10 wherein the weight ratio of phosphorus derived from the ashless organo-phosphorus compound to phosphorus dervied from the zinc thiophosphate compound is from 10:1 to 1:20, preferably from 5:1 to 1:15.
    12. Use of a combination of additives as an antiwear agent in a lubricant composition, the combination of additives being in accordance with any one of claims 1 to 5.
    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

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

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    DE112011103822T5 (en) 2010-11-19 2013-08-22 Chevron U.S.A. Inc. Lubricant for percussion equipment

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    KR20030090891A (en) * 2002-05-22 2003-12-01 현대자동차주식회사 Composition of gear oil for automobiles
    KR100488860B1 (en) * 2002-07-25 2005-05-11 현대자동차주식회사 Compostion for variable continuously transmission fluid
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    ES2128581T3 (en) 1999-05-16
    CA2171538A1 (en) 1995-03-23
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    DE69415817D1 (en) 1999-02-18
    ATE175438T1 (en) 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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