EP2251401A2 - Formulations de lubrifiant et procédés - Google Patents

Formulations de lubrifiant et procédés Download PDF

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Publication number
EP2251401A2
EP2251401A2 EP10161225A EP10161225A EP2251401A2 EP 2251401 A2 EP2251401 A2 EP 2251401A2 EP 10161225 A EP10161225 A EP 10161225A EP 10161225 A EP10161225 A EP 10161225A EP 2251401 A2 EP2251401 A2 EP 2251401A2
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Prior art keywords
lubricant composition
compound
phosphorus
hydrocarbon soluble
metal compound
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EP10161225A
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German (de)
English (en)
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EP2251401A3 (fr
Inventor
Naresh C. Mathur
Gregory H. Guinther
Jeffrey M Guevremont
Jason Lagona
Mark T. Devlin
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Afton Chemical Corp
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Afton Chemical Corp
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Publication of EP2251401A2 publication Critical patent/EP2251401A2/fr
Publication of EP2251401A3 publication Critical patent/EP2251401A3/fr
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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
    • 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
    • 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
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/1006Petroleum or coal fractions, e.g. tars, solvents, bitumen used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/102Aliphatic fractions
    • C10M2203/1025Aliphatic fractions used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/028Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms
    • C10M2205/0285Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms used as base material
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/08Aldehydes; Ketones
    • 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
    • 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
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/06Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/40Low content or no content compositions
    • C10N2030/42Phosphor free or low phosphor content compositions
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/40Low content or no content compositions
    • C10N2030/43Sulfur free or low sulfur content compositions
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/40Low content or no content compositions
    • C10N2030/45Ash-less or low ash content
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/54Fuel economy
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/56Boundary lubrication or thin film lubrication
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/70Soluble oils
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/25Internal-combustion engines
    • 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

  • the embodiments described herein relate to particular formulations and methods that provide improved lubricant performance for internal combustion engines.
  • ZDDP zinc dialkyldithiophosphate
  • the additive is truly ubiquitous and found in nearly every modem engine oil.
  • ZDDP may impart multifunctional performance in the areas of anti-wear, anti-oxidation, and anticorrosion and is considered one of the most cost-effective additives in general use by engine oil manufacturers and marketers.
  • ZDDP may form a thick glassy polyphosphate film that is effective to prevent wear between metal parts of an engine.
  • compositions and methods include a (a) a base oil; (b) a zinc dialkyldithiophosphate compound; and (c) a hydrocarbon soluble metal compound.
  • the hydrocarbon soluble metal compound is devoid of phosphorus and sulfur atoms and the metal is selected from the group consisting essentially of cobalt, nickel, zinc, zirconium, manganese, vanadium, scandium, yttrium, tungsten, gold, platinum, and iron.
  • a weight ratio of total metal in the lubricant composition from the zinc dialkyldithiophosphate compound and the hydrocarbon soluble metal compound to phosphorus in the lubricant composition ranges from greater than 1.5 to 1 to 15 to 1.
  • An embodiment of the disclosure may provide additive concentrate for an engine crankcase lubricant.
  • the additive concentrate includes a zinc dialkyldithiophosphate compound, and a hydrocarbon soluble metal compound other than a dispersant or a detergent.
  • the hydrocarbon soluble metal compound is devoid of phosphorus and sulfur atoms and the metal is selected from the group consisting essentially of cobalt, nickel, zinc, zirconium, manganese, vanadium, scandium, yttrium, tungsten, gold, platinum, and iron.
  • a weight ratio of total metal in the concentrate from the zinc dialkyldithiophosphate compound and the hydrocarbon soluble metal compound to phosphorus in the concentrate ranges from greater than 1.5 to 1 to 15 to 1.
  • the engine is lubricated with a lubricant composition that includes, (a) a base oil; (b) a zinc dialkyldithiophosphate compound; and (b) a hydrocarbon soluble metal compound other than a dispersant or a detergent.
  • the hydrocarbon soluble metal compound is devoid of phosphorus and sulfur atoms and the metal is selected from the group consisting essentially of zinc cobalt, nickel, zinc, zirconium, manganese, vanadium, scandium, yttrium, tungsten, gold, platinum, and iron.
  • a weight ratio of total metal in the concentrate from the zinc dialkyl- dithiophosphate compound and the hydrocarbon soluble metal compound to phosphorus in the lubricant composition ranges from greater than 1.5 to 1 to 15 to 1.
  • the engine is lubricated with a lubricant composition that includes, (a) a base oil; (b) a zinc dialkyldithiophosphate compound; and (b) a hydrocarbon soluble metal compound other than a dispersant or a detergent.
  • the hydrocarbon soluble metal compound is devoid of phosphorus and sulfur atoms and the metal is selected from the group consisting essentially of cobalt, nickel, zinc, zirconium, manganese, vanadium, scandium, yttrium, tungsten, gold, platinum, and iron.
  • a weight ratio of total metal in the concentrate from the zinc dialkyldithiophosphate compound and the hydrocarbon soluble metal compound to phosphorus in the lubricant composition ranges from greater than 1.5 to 1 to 15 to 1.
  • compositions and methods described may be particularly suitable for improving boundary friction characteristics of lubricant compositions containing from 100 to 1000 ppm phosphorus from a zinc dialkyldithiophosphate compound without adversely affecting thin film friction characteristics of the lubricant composition.
  • Other features and advantages of the compositions and methods described herein may be evident by reference to the following detailed description which is intended to exemplify aspects of the embodiments without intending to limit the embodiments described herein.
  • Lubricant compositions may comprise a base oil; a zinc dialkyldithiophosphate (ZDDP) compound and a hydrocarbon soluble metal compound, wherein the metal of the metal compound is a transition metal selected from cobalt, nickel, zinc, zirconium, manganese, vanadium, scandium, yttrium, tungsten, gold, platinum, and iron. It is particularly desirable that the transition metal compound be substantially devoid of phosphorus and sulfur atoms.
  • the lubricant composition may also include other hydrocarbon soluble metal compounds, such as organomolybdenum compounds that are devoid of phosphorus and sulfur atoms. However, for purposes of this disclosure, the metal to phosphorus weight ratio is determined on the basis of the ZDDP and the hydrocarbon soluble transition metal compounds described above. Lubricant compositions of the disclosure are also substantially devoid of non-metal containing phosphorus compounds.
  • the lubricant compositions may be suitable for use in a variety of applications, including but not limited to engine oil applications and/or heavy duty engine oil applications. Examples may include the crankcase of spark-ignited and compression-ignited internal combustion engines, automobile and truck engines, marine and railroad diesel engines, and the like.
  • the lubricant compositions may comprise a base oil and one or more suitable additive components.
  • the additive components may be combined to form an additive package which is combined with the base oil. Or, alternatively, the additive components may be combined directly with the base oil.
  • Base oils suitable for use with present embodiments may comprise one or more oils of lubricating viscosity such as mineral (or natural) oils, synthetic lubricating oils, vegetable oils, and mixtures thereof.
  • Such base oils include those conventionally employed as crankcase lubricating oils for spark-ignited and compression-ignited internal combustion engines, such as automobile and truck engines, marine and railroad diesel engines, and the like.
  • Suitable base oils may have a NOACK volatility of from 5 to 15.
  • suitable base oils may have a NOACK volatility of from 10 to 15.
  • suitable base oils may have a NOACK volatility of from 9 to 13.
  • Base oils are typically classified as Group I, Group II, Group III, Group IV and Group V, as described in Table 1 below.
  • Table 1 Group I-V Base Oils Base Oil % Sulfur % Saturates Viscosity Index Group I > 0.03 and/or ⁇ 90 80-120 Group II ⁇ 0.03 and/or ⁇ 90 80-120 Group III ⁇ 0.03 and/or ⁇ 90 ⁇ 120 Group IV * Group V ** * Group IV base oils are defined as all polyalphaolefins ** Group V base oils are defined as all other base oils not included in Groups I, II, III and IV and may include gas to liquid base oils.
  • Lubricating base oils may also include oils made from a waxy feed.
  • the waxy feed may comprise at least 40 weight percent n-paraffins, for example greater than 50 weight percent n-paraffins, and more desirably greater than 75 weight percent n-paraffins.
  • the waxy feed may be a conventional petroleum derived feed, such as, for example, slack wax, or it may be derived from a synthetic feed, such as, for example, a feed prepared from a Fischer-Tropsch synthesis.
  • Non-limiting examples of synthetic base oils include alkyl esters of dicarboxylic acids, polyglycols and alcohols, poly-alpha-olefins, including polybutenes, alkyl benzenes, organic esters of phosphoric acids, polysilicone oils, and alkylene oxide polymers, interpolymers, copolymers and derivatives thereof where the terminal hydroxyl groups have been modified by esterification, etherification, and the like.
  • Mineral base oils include, but are not limited to, animal oils and vegetable oils (e.g., castor oil, lard oil), liquid petroleum oils and hydrorefined, solvent-treated or acid-treated mineral lubricating oils of the paraffinic, naphthenic and mixed paraffinic-naphthenic types. Oils of lubricating viscosity derived from coal or shale are also useful base oils.
  • a primary component of the lubricant composition is a phosphorus-containing metal compound such as ZDDP.
  • Suitable ZDDPs may be prepared from specific amounts of primary or secondary alcohols, or mixtures thereof.
  • the alcohols may be combined in a ratio of from 100:0 to 0:100 primary-to-secondary alcohols.
  • the alcohols may be combined in a ratio of 60:40 primary-to-secondary alcohols.
  • An example of a suitable ZDDP may comprise the reaction product obtained by combining: (i) 50 to 100 mol % of C 1 to C 18 primary alcohol; (ii) up to 50 mol % of C 3 to C 18 secondary alcohol; (iii) a phosphorus-containing component; and (iv) a zinc-containing component.
  • the primary alcohol may be a mixture of from C 1 to C 18 alcohols.
  • the primary alcohol may be a mixture of a C 4 and a C 8 alcohol.
  • the secondary alcohol may also be a mixture of alcohols.
  • the secondary alcohol may comprise a C 3 -C 6 alcohol.
  • the alcohols may contain any of branched, cyclic, or straight chains.
  • the ZDDP may comprise the combination of 60 mol % primary alcohol and 40 mol % secondary alcohol. In the alternative, the ZDDP may comprise 100 mol % secondary alcohols, or 100 mol % primary alcohols.
  • the phosphorus-containing component used to make the ZDDP compound may comprise any suitable phosphorus-containing component such as, but not limited to a phosphorus sulfide.
  • Suitable phosphorus sulfides may include phosphorus pentasulfide or tetraphosphorus trisulfide.
  • the zinc-containing component used to make the ZDDP compound may comprise any suitable zinc-containing component such as, but not limited to zinc oxide, zinc hydroxide, zinc carbonate, zinc propylate, zinc chloride, zinc propionate, or zinc acetate.
  • the reaction product may comprise a resulting mixture, component, or mixture of components.
  • the reaction product may or may not include unreacted reactants, chemically bonded components, products, or polar bonded components.
  • the ZDDP compound may be present in an amount sufficient to contribute from 0.03 wt% to 0.15 wt% phosphorus in the lubricant composition.
  • the hydrocarbon soluble metal compounds that are used in combination with the ZDDP compound to provide lubricants having improved friction characteristics may include a wide variety of transition metal compounds that are soluble in hydrocarbons such as natural and synthetic lubricating oils.
  • suitable transition metals for the hydrocarbon soluble metal compounds include, but are not limited to cobalt, nickel, zinc, zirconium, manganese, vanadium, scandium, yttrium, tungsten, gold, platinum, and iron.
  • the metal compounds may be selected from metal alkoxides, carboxylates, acetylacetonates, amoinocarboxylates, aminoacetylacetonates, naphthenates, and polymeric derivatives thereof containing M-O-M linkages, wherein M is the metal of the metal compound.
  • the transition metal compound is substantially devoid of sulfur and phosphorus atoms.
  • the metal carboxylates may be derived from carboxylic acids.
  • the carboxylic acids may be mono-or polycarboxylic acids such as di- or tricarboxylic acids.
  • Monocarboxylic acids include C 1-7 lower acids (acetic, proprionic, etc.) and higher C 8+ acids (e.g., octanoic, decanoic, etc.) as well as the fatty acids of 12-30 carbon atoms.
  • the neo acids such as neooctanoic and neodecanoic and the like are also useful.
  • Fatty acids are often mixtures of straight and branched chain acids containing, for example, from 5% to 30% straight chain acids and 70% to 95% (mole) branched chain acids. Other commercially available fatty acid mixtures containing much higher proportions of straight chain acids are also useful. Mixtures produced from dimerization of unsaturated fatty acids can also be used.
  • aminocarboxylic acids examples include, but not limited to, ethylenediaminetetraacetic acid (EDTA), trans-1,2-diaminocyclohexane-N,N,N',N'-tetraacetic acid (CDTA), ethylenediaminedisuccinic acid (EDDS), diethylenetriaminepentaacetic acid (DTPA), triethylenetetraarninehexaacetic acid (TTHA) and ethylenebis [2(hydroxyphenyl) glycine] (EDDHA).
  • EDTA ethylenediaminetetraacetic acid
  • CDTA trans-1,2-diaminocyclohexane-N,N,N',N'-tetraacetic acid
  • EDDS ethylenediaminedisuccinic acid
  • DTPA diethylenetriaminepentaacetic acid
  • TTHA triethylenetetraarninehexaacetic acid
  • ETDHA ethylenebis [2(hydroxyphenyl) g
  • Acetylacetonates, tert-butyl acetylacetonates may be used as the metal compounds.
  • a particularly suitable hydrocarbon soluble metal compound is a metal chelate with 2,2,6,6-tetramethyl-3,5-heptanedionate ligands.
  • the amount of metal compound used in the lubricant composition in combination with the ZDDP compound is that amount of compound which is sufficient to provide a total metal content, based on ZDDP and the metal compound of from 300 to 1500 ppm by weight based on the total weight of the lubricant composition. Accordingly, the weight ratio of total metal to phosphorus in the lubricant composition, based on the ZDDP and hydrocarbon soluble transition metal compound may range from above 1.5 to 1 to 15 to 1 or higher. In another embodiment, the weight ratio of total metal to phosphorus may range from 3 to 1 to 10 to 1.
  • the ZDDP compound and transition metal compound mixture disclosed herein is used in combination with other additives.
  • the additives are typically blended into the base oil in an amount that enables that additive to provide its desired function.
  • Representative effective amounts of the phosphorus-containing and transition metal compound mixtures and additives, when used in crankcase lubricants, are listed in Table 2 below. All the values listed are stated as weight percent active ingredient.
  • Table 2 Component Wt. % (Broad) Wt.
  • Dispersants that may be used in an additive package with the ZDDP and metal compounds include, but are not limited to, ashless dispersants that have an oil soluble polymeric hydrocarbon backbone having functional groups that are capable of associating with particles to be dispersed. Typically, the dispersants comprise amine, alcohol, amide, or ester polar moieties attached to the polymer backbone often via a bridging group. Dispersants may be selected from Mannich dispersants as described in U.S. Pat. Nos. 3,697,574 and 3,736,357 ; ashless succcinimide dispersants as described in U.S. Pat. Nos. 4,234,435 and 4,636,322 ; amine dispersants as described in U.S. Pat.
  • Oxidation inhibitor may also be used in combination with the ZDDP and metal compounds in a lubricant additive package. Oxidation inhibitors or antioxidants reduce the tendency of base stocks to deteriorate in service which deterioration can be evidenced by the products of oxidation such as sludge and varnish-like deposits that deposit on metal surfaces and by viscosity growth of the finished lubricant.
  • Such oxidation inhibitors include hindered phenols, sulfurized hindered phenols, alkaline earth metal salts of alkylphenolthioesters having C 5 to C 12 alkyl side chains, sulfurized alkylphenols, metal salts of either sulfurized or nonsulfurized alkylphenols, for example calcium nonylphenol sulfide, ashless oil soluble phenates and sulfurized phenates, phosphosulfurized or sulfurized hydrocarbons, phosphorus esters, metal thiocarbamates, and oil soluble copper compounds as described in U.S. Pat. No. 4,867,890 .
  • antioxidants that may be used include diarylamines, alkylated phenothiazines, sulfurized compounds, and ashless dialkyldithiocarbamates. Sterically hindered phenols and mixtures thereof as described in U.S Publication No. 2004/0266630 .
  • Diarylamine antioxidants include, but are not limited to diarylamines having the formula: wherein R' and R" each independently represents a substituted or unsubstituted aryl group having from 6 to 30 carbon atoms.
  • substituents for the aryl group include aliphatic hydrocarbon groups such as alkyl having from 1 to 30 carbon atoms, hydroxy groups, halogen radicals, carboxylic acid or ester groups, or nitro groups.
  • Another class of aminic antioxidants includes phenothiazine or alkylated phenothiazine having the chemical formula: wherein R 1 is a linear or branched C 1 to C 24 alkyl, aryl, heteroalkyl or alkylaryl group and R 2 is hydrogen or a linear or branched C 1 - C 24 alkyl, heteroalkyl, or alkylaryl group.
  • the sulfur containing antioxidants include, but are not limited to, sulfurized olefins that are characterized by the type of olefin used in their production and the final sulfur content of the antioxidant.
  • High molecular weight olefins i.e. those olefins having an average molecular weight of 168 to 351 g/mole, are preferred.
  • Examples of olefins that may be used include alpha-olefins, isomerized alpha-olefins, branched olefins, cyclic olefins, and combinations of these.
  • Sulfur sources that may be used in the sulfurization reaction of olefins include: elemental sulfur, sulfur monochloride, sulfur dichloride, sodium sulfide, sodium polysulfide, and mixtures of these added together or at different stages of the sulfurization process.
  • Unsaturated oils because of their unsaturation, may also be sulfurized and used as an antioxidant.
  • oils or fats that may be used include corn oil, canola oil, cottonseed oil, grapeseed oil, olive oil, palm oil, peanut oil, coconut oil, rapeseed oil, safflower seed oil, sesame seed oil, soyabean oil, sunflower seed oil, tallow, and combinations of these.
  • the foregoing aminic, phenothiazine, and sulfur containing antioxidants are described for example in U.S. Pat. No. 6,599,865 .
  • the ashless dialkyldithiocarbamates which may be used as antioxidant additives include compounds that are soluble or dispersable in the additive package. It is also preferred that the ashless dialkyldithiocarbamate be of low volatility, preferably having a molecular weight greater than 250 daltons, most preferably having a molecular weight greater than 400 daltons. Examples of dialkyldithiocarbamates that may be used are disclosed in the following patents: U.S. Pat Nos.
  • Organomolybdenum containing compounds used as friction modifiers may also exhibit antioxidant functionality.
  • U.S. Pat. No. 6,797,677 describes a combination of organomolybdenum compound, alkylphenothiazine and alkyldiphenylamines for use in finished lubricant formulations. Examples of suitable molybdenum containing friction modifiers are described below under friction modifiers.
  • a sulfur- and phosphorus-free organomolybdenum compound that may be used as a friction modifier may be prepared by reacting a sulfur- and phosphorus-free molybdenum source with an organic compound containing amino and/or alcohol groups.
  • sulfur- and phosphorus-free molybdenum sources include molybdenum trioxide, ammonium molybdate, sodium molybdate and potassium molybdate.
  • the amino groups may be monoamines, diamines, or polyamines.
  • the alcohol groups may be mono-substituted alcohols, diols or bis-alcohols, or polyalcohols.
  • the reaction of diamines with fatty oils produces a product containing both amino and alcohol groups that can react with the sulfur- and phosphorus-free molybdenum source.
  • sulfur- and phosphorus-free organomolybdenum compounds include compounds described in the following patents: U. S. Pat. Nos. 4,259,195 ; 4,261,843 ; 4,164,473 ; 4,266,945 ; 4,889,647 ; 5,137,647 ; 4,692,256 ; 5,412,130 ; 6,509,303 ; and 6,528,463 .
  • Molybdenum compounds prepared by reacting a fatty oil, diethanolamine, and a molybdenum source as described in U. S. Pat. No. 4,889,647 are sometimes illustrated with the following structure, where R is a fatty alkyl chain, although the exact chemical composition of these materials is not fully known and may in fact be multi-component mixtures of several organomolybdenum compounds.
  • Sulfur-containing organomolybdenum compounds may be used and may be prepared by a variety of methods.
  • One method involves reacting a sulfur and phosphorus-free molybdenum source with an amino group and one or more sulfur sources.
  • Sulfur sources can include for example, but are not limited to, carbon disulfide, hydrogen sulfide, sodium sulfide and elemental sulfur.
  • the sulfur-containing molybdenum compound may be prepared by reacting a sulfur-containing molybdenum source with an amino group or thiuram group and optionally a second sulfur source
  • sulfur-containing organomolybdenum compounds include compounds described in the following patents: U. S. Pat. Nos. 3,509,051 ; 3,356,702 ; 4,098,705 ; 4,178,258 ; 4,263,152 ; 4,265,773 ; 4,272,387 ; 4,285,822 ; 4,369,119 ; 4,395,343 ; 4,283,295 ; 4,362,633 ; 4,402,840 ; 4,466,901 ; 4,765,918 ; 4,966,719 ; 4,978,464 ; 4,990,271 ; 4,995,996 ; 6,232,276 ; 6,103,674 ; and 6,117,826 .
  • Glycerides may also be used alone or in combination with other friction modifiers. Suitable glycerides include glycerides of the formula: wherein each R is independently selected from the group consisting of H and C(O)R' where R' may be a saturated or an unsaturated alkyl group having from 3 to 23 carbon atoms. Examples of glycerides that may be used include glycerol monolaurate, glycerol monomyristate, glycerol monopalmitate, glycerol monostearate, and mono-glycerides derived from coconut acid, tallow acid, oleic acid, linoleic acid, and linolenic acids.
  • Typical commercial monoglycerides contain substantial amounts of the corresponding diglycerides and triglycerides. These materials are not detrimental to the production of the molybdenum compounds, and may in fact be more active. Any ratio of mono- to di-glyceride may be used, however, it is preferred that from 30 to 70% of the available sites contain free hydroxyl groups (i.e., 30 to 70% of the total R groups of the glycerides represented by the above formula are hydrogen).
  • a preferred glyceride is glycerol monooleate, which is generally a mixture of mono, di, and tri-glycerides derived from oleic acid, and glycerol.
  • Rust inhibitors selected from the group consisting of nonionic polyoxyalkylene polyols and esters thereof, polyoxyalkylene phenols, and anionic alkyl sulfonic acids may be used.
  • a small amount of a demulsifying component may be used.
  • a preferred demulsifying component is described in EP 330,522 .
  • Such demulsifying component may be obtained by reacting an alkylene oxide with an adduct obtained by reacting a bis-epoxide with a polyhydric alcohol.
  • the demulsifier should be used at a level not exceeding 0.1 mass % active ingredient.
  • a treat rate of 0.001 to 0.05 mass % active ingredient is convenient.
  • Pour point depressants otherwise known as lube oil flow improvers, lower the minimum temperature at which the fluid will flow or can be poured.
  • Such additives are well known. Typical of those additives which improve the low temperature fluidity of the fluid are C 8 to C 18 dialkyl fumarate/vinyl acetate copolymers, polyalkylmethacrylates and the like.
  • Foam control can be provided by many compounds including an antifoamant of the polysiloxane type, for example, silicone oil or polydimethyl siloxane.
  • Seal swell agents as described, for example, in U.S. Patent Nos. 3,794,081 and 4,029,587 , may also be used.
  • Viscosity modifiers function to impart high and low temperature operability to a lubricating oil.
  • the VM used may have that sole function, or may be multifunctional.
  • Multifunctional viscosity modifiers that also function as dispersants are also known.
  • Suitable viscosity modifiers are polyisobutylene, copolymers of ethylene and propylene and higher alpha-olefins, polymethacrylates, polyalkylmethacrylates, methacrylate copolymers, copolymers of an unsaturated dicarboxylic acid and a vinyl compound, inter polymers of styrene and acrylic esters, and partially hydrogenated copolymers of styrene/isoprene, styrene/butadiene, and isoprene/butadiene, as well as the partially hydrogenated homopolymers of butadiene and isoprene and isoprene/divinylbenzene.
  • Functionalized olefin copolymers that may be used include interpolymers of ethylene and propylene which are grafted with an active monomer such as maleic anhydride and then derivatized with an alcohol or amine.
  • Other such copolymers are copolymers of ethylene and propylene which are grafted with nitrogen compounds.
  • each of the foregoing additives when used, is used at a functionally effective amount to impart the desired properties to the lubricant.
  • a functionally effective amount of this corrosion inhibitor would be an amount sufficient to impart the desired corrosion inhibition characteristics to the lubricant.
  • the concentration of each of these additives, when used ranges up to 20% by weight based on the weight of the lubricating oil composition, and in one embodiment from 0.001 % to 20% by weight, and in one embodiment 0.01 % to 10% by weight based on the weight of the lubricating oil composition.
  • the ZDDP and hydrocarbon soluble metal compounds may be added directly to the lubricating oil composition. In one embodiment, however, they are diluted with a substantially inert, normally liquid organic diluent such as mineral oil, synthetic oil, naphtha, alkylated (e.g. C 10 to C 13 alkyl) benzene, toluene or xylene to form an additive concentrate. These concentrates usually contain from 1% to 100% by weight and in one embodiment 10% to 90% by weight of the additive mixture.
  • a substantially inert, normally liquid organic diluent such as mineral oil, synthetic oil, naphtha, alkylated (e.g. C 10 to C 13 alkyl) benzene, toluene or xylene.
  • These concentrates usually contain from 1% to 100% by weight and in one embodiment 10% to 90% by weight of the additive mixture.
  • Inventive and comparative lubricant compositions containing the ZDDP compound and metal compound were tested to provide boundary friction characteristics and thin film friction characteristics.
  • the friction characteristics of the compositions were determined using a Mini Traction Machine with a Spacer Layer Imaging System (MTM-SLIM).
  • MTM-SLIM Spacer Layer Imaging System
  • the metal compounds were added to the mixture in the form of a chelate of 2,2,6,6,-tetramethyl-3,5-heptanedionate ligands.
  • the results of each mixture are given in the following table.
  • the foregoing table 3 illustrates that increasing an amount of ZDDP compound to provide from 400 ppm total metal to 600 ppm total metal significantly increase boundary friction from 0.150 at 400 ppm total metal to 0.178 at 600 ppm total metal.
  • the boundary friction is about the same or lower than with 400 ppm total metal and only ZDDP in the lubricant composition.
  • increasing the metal to phosphorus ratio to above about 1.5 to 1 in a lubricant composition using a non-phosphorus metal compound may be useful for increasing engine fuel economy.
  • ZDDP 400 ppm P ---- 400 1 to 1 0.042 ZDDP, 600 ppm P ---- 600 1 to 1 0.045 ZDDP, 400 ppm P 40 ppm Zn 440 1.1 to 1 0.040 ZDDP, 400 ppm P 200 ppm Zn 600 1.5 to 1 0.043 ZDDP, 400 ppm P 400 ppm Zn 800 2 to 1 0.041 ZDDP, 400 ppm P 4000 ppm Zn 4400 11 to 1 0.024 ZDDP, 400 ppm P 200 ppm Ti 600 1.5 to 1 0.045 ZDDP, 400 ppm P 200 ppm Fe 600 1.5 to 1 0.040 ZDDP, 400 ppm P 200 ppm Ca 600 1.5 to 1 0.056 ZDDP, 400 ppm P 200 ppm Zr 600 1.5 to 1 0.038
  • non-transition metals such as calcium
  • ZDDP zinc-doped aluminum
  • a transition metal compound such as Zn, Ti, Fe, or Zr.

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  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2019012447A1 (fr) * 2017-07-14 2019-01-17 Chevron Oronite Company Llc Compositions d'huile lubrifiante contenant du zirconium et procédé pour empêcher ou réduire le préallumage à faible vitesse dans des moteurs à allumage par étincelle à injection directe

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015021129A1 (fr) * 2013-08-09 2015-02-12 The Lubrizol Corporation Dépôts de moteur réduits grâce à un agent de dispersion traité au cobalt
US20240141252A1 (en) 2022-10-11 2024-05-02 Benjamin G. N. Chappell Lubricant Composition Containing Metal Alkanoate

Citations (66)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2384577A (en) 1944-03-03 1945-09-11 Du Pont Esters
US2710872A (en) 1954-04-12 1955-06-14 Universal Oil Prod Co Production of esters of dithiocarbamic acid
US2786866A (en) 1952-06-11 1957-03-26 American Cyanamid Co Esters of dithiocarbamic acids and a method for their preparation
US2897152A (en) 1956-03-08 1959-07-28 Wakefield & Co Ltd C C Lubricating oils
US3219666A (en) 1959-03-30 1965-11-23 Derivatives of succinic acids and nitrogen compounds
US3356702A (en) 1964-08-07 1967-12-05 Vanderbilt Co R T Molybdenum oxysulfide dithiocarbamates and processes for their preparation
US3407222A (en) 1965-08-24 1968-10-22 American Cyanamid Co Preparation of 2-hydroxyalkyldithio carbamates from epoxides and amine salts of dithio-carbamic acid
US3509051A (en) 1964-08-07 1970-04-28 T R Vanderbilt Co Inc Lubricating compositions containing sulfurized oxymolybdenum dithiocarbamates
US3565804A (en) 1965-08-23 1971-02-23 Chevron Res Lubricating oil additives
US3697574A (en) 1965-10-22 1972-10-10 Standard Oil Co Boron derivatives of high molecular weight mannich condensation products
US3736357A (en) 1965-10-22 1973-05-29 Standard Oil Co High molecular weight mannich condensation products from two different alkyl-substituted hydroxy-aromatic compounds
US3794081A (en) 1972-05-05 1974-02-26 Smith Inland A O Fiber reinforced tubular article having abrasion resistant liner
US3867359A (en) 1973-11-16 1975-02-18 R F Vanderbilt Company Inc Process of vulcanizing neoprene by using certain 2-hydroxyalkyl N,N-dialkyldithiocarbamates as accelerators
US4029587A (en) 1975-06-23 1977-06-14 The Lubrizol Corporation Lubricants and functional fluids containing substituted sulfolanes as seal swelling agents
US4098705A (en) 1975-08-07 1978-07-04 Asahi Denka Kogyo K.K. Sulfur containing molybdenum dihydrocarbyldithiocarbamate compound
US4164473A (en) 1977-10-20 1979-08-14 Exxon Research & Engineering Co. Organo molybdenum friction reducing antiwear additives
US4178258A (en) 1978-05-18 1979-12-11 Edwin Cooper, Inc. Lubricating oil composition
US4234435A (en) 1979-02-23 1980-11-18 The Lubrizol Corporation Novel carboxylic acid acylating agents, derivatives thereof, concentrate and lubricant compositions containing the same, and processes for their preparation
US4259195A (en) 1979-06-28 1981-03-31 Chevron Research Company Reaction product of acidic molybdenum compound with basic nitrogen compound and lubricants containing same
US4261843A (en) 1979-06-28 1981-04-14 Chevron Research Company Reaction product of acidic molybdenum compound with basic nitrogen compound and lubricants containing same
US4263152A (en) 1979-06-28 1981-04-21 Chevron Research Company Process of preparing molybdenum complexes, the complexes so-produced and lubricants containing same
US4265773A (en) 1979-06-28 1981-05-05 Chevron Research Company Process of preparing molybdenum complexes, the complexes so-produced and lubricants containing same
US4266945A (en) 1979-11-23 1981-05-12 The Lubrizol Corporation Molybdenum-containing compositions and lubricants and fuels containing them
US4272387A (en) 1979-06-28 1981-06-09 Chevron Research Company Process of preparing molybdenum complexes, the complexes so-produced and lubricants containing same
US4283295A (en) 1979-06-28 1981-08-11 Chevron Research Company Process for preparing a sulfurized molybdenum-containing composition and lubricating oil containing said composition
US4285822A (en) 1979-06-28 1981-08-25 Chevron Research Company Process for preparing a sulfurized molybdenum-containing composition and lubricating oil containing the composition
US4362633A (en) 1980-10-10 1982-12-07 Standard Oil Company (Indiana) Molybdenum-containing aminated sulfurized olefin lubricating oil additives
US4369119A (en) 1981-04-03 1983-01-18 Chevron Research Company Antioxidant combinations of molybdenum complexes and organic sulfur compounds for lubricating oils
US4395343A (en) 1981-08-07 1983-07-26 Chevron Research Company Antioxidant combinations of sulfur containing molybdenum complexes and organic sulfur compounds
US4402840A (en) 1981-07-01 1983-09-06 Chevron Research Company Antioxidant combinations of molybdenum complexes and organic sulfur compounds for lubricating oils
US4466901A (en) 1982-06-11 1984-08-21 Standard Oil Company (Indiana) Molybdenum-containing friction modifying additive for lubricating oils
US4636322A (en) 1985-11-04 1987-01-13 Texaco Inc. Lubricating oil dispersant and viton seal additives
US4692256A (en) 1985-06-12 1987-09-08 Asahi Denka Kogyo K.K. Molybdenum-containing lubricant composition
US4758362A (en) 1986-03-18 1988-07-19 The Lubrizol Corporation Carbamate additives for low phosphorus or phosphorus free lubricating compositions
US4765918A (en) 1986-11-28 1988-08-23 Texaco Inc. Lubricant additive
EP0330522A2 (fr) 1988-02-26 1989-08-30 Exxon Chemical Patents Inc. Compositions démulsionnées d'huiles lubrifiantes
US4867890A (en) 1979-08-13 1989-09-19 Terence Colclough Lubricating oil compositions containing ashless dispersant, zinc dihydrocarbyldithiophosphate, metal detergent and a copper compound
US4876375A (en) 1988-05-02 1989-10-24 Ethyl Petroleum Additives, Inc. Norbornyl dithiocarbamates
US4885365A (en) 1988-05-20 1989-12-05 Ethyl Petroleum Additives, Inc. Dithiocarbanate lubricant compositions
US4889647A (en) 1985-11-14 1989-12-26 R. T. Vanderbilt Company, Inc. Organic molybdenum complexes
US4927552A (en) 1988-05-02 1990-05-22 Ethyl Petroleum Additives, Inc. Lubricating oil composition
US4957643A (en) 1988-05-20 1990-09-18 Ethyl Petroleum Additives, Inc. Lubricant compositions
US4966719A (en) 1990-03-12 1990-10-30 Exxon Research & Engineering Company Multifunctional molybdenum and sulfur containing lube additives
US4978464A (en) 1989-09-07 1990-12-18 Exxon Research And Engineering Company Multi-function additive for lubricating oils
US4990271A (en) 1989-09-07 1991-02-05 Exxon Research And Engineering Company Antiwear, antioxidant and friction reducing additive for lubricating oils
US4995996A (en) 1989-12-14 1991-02-26 Exxon Research And Engineering Company Molybdenum sulfur antiwear and antioxidant lube additives
US5137647A (en) 1991-12-09 1992-08-11 R. T. Vanderbilt Company, Inc. Organic molybdenum complexes
US5412130A (en) 1994-06-08 1995-05-02 R. T. Vanderbilt Company, Inc. Method for preparation of organic molybdenum compounds
US5627259A (en) 1994-06-17 1997-05-06 Exxon Chemical Patents Inc. Amidation of ester functionalized hydrocarbon polymers
US5633326A (en) 1989-12-13 1997-05-27 Exxon Chemical Patents Inc. Polyolefin-substituted amines grafted with poly(aromatic-N-monomers) for oleaginous compositions
US5643859A (en) 1992-12-17 1997-07-01 Exxon Chemical Patents Inc. Derivatives of polyamines with one primary amine and secondary of tertiary amines
US5686397A (en) 1997-02-03 1997-11-11 Uniroyal Chemical Company, Inc. Dithiocarbamate derivatives and lubricants containing same
US5693598A (en) 1995-09-19 1997-12-02 The Lubrizol Corporation Low-viscosity lubricating oil and functional fluid compositions
US5789357A (en) 1997-01-10 1998-08-04 Uniroyal Chemical Company, Inc. Dithiocarbamyl carboxylic acids and their use as multifunctional additives for lubricating oils
US5792729A (en) 1996-08-20 1998-08-11 Chevron Chemical Corporation Dispersant terpolymers
US5851965A (en) 1995-12-01 1998-12-22 Chevron Chemical Company Dispersant compositions having polyalkylene succinimides
US5902776A (en) 1995-09-19 1999-05-11 The Lubrizol Corporation Additive compositions for lubricants and functional fluids
US5936041A (en) 1994-06-17 1999-08-10 Exxon Chemical Patents Inc Dispersant additives and process
US6103674A (en) 1999-03-15 2000-08-15 Uniroyal Chemical Company, Inc. Oil-soluble molybdenum multifunctional friction modifier additives for lubricant compositions
US6117826A (en) 1998-09-08 2000-09-12 Uniroyal Chemical Company, Inc. Dithiocarbamyl derivatives useful as lubricant additives
US6232276B1 (en) 1996-12-13 2001-05-15 Infineum Usa L.P. Trinuclear molybdenum multifunctional additive for lubricating oils
US6509303B1 (en) 2000-03-23 2003-01-21 Ethyl Corporation Oil soluble molybdenum additives from the reaction product of fatty oils and monosubstituted alkylene diamines
US6528463B1 (en) 2000-03-23 2003-03-04 Ethyl Corporation Oil soluble molybdenum compositions
US6599865B1 (en) 2002-07-12 2003-07-29 Ethyl Corporation Effective antioxidant combination for oxidation and deposit control in crankcase lubricants
US6797677B2 (en) 2002-05-30 2004-09-28 Afton Chemical Corporation Antioxidant combination for oxidation and deposit control in lubricants containing molybdenum and alkylated phenothiazine
US20040266630A1 (en) 2003-06-25 2004-12-30 The Lubrizol Corporation, A Corporation Of The State Of Ohio Novel additive composition that reduces soot and/or emissions from engines

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB921124A (en) * 1959-12-15 1963-03-13 Exxon Research Engineering Co Process for preparing petroleum oil additives
US3791804A (en) * 1969-10-10 1974-02-12 Standard Oil Co Fuel and lubricating oil additives transition metal complexes
US4171268A (en) * 1978-05-22 1979-10-16 Mooney Chemicals, Inc. Lubricant compositions containing zirconyl soaps
US4555352A (en) * 1983-04-08 1985-11-26 Power-Aid Industries (1980) Ltd. Lubricant additive
DE3610205A1 (de) * 1986-03-26 1987-10-01 Tribol Lubricants Gmbh Schmiermittel und verfahren zu dessen herstellung
US4904401A (en) * 1988-06-13 1990-02-27 The Lubrizol Corporation Lubricating oil compositions
GB2293389A (en) * 1994-09-26 1996-03-27 Ethyl Petroleum Additives Ltd Mixed zinc salt lubricant additives
JP3927724B2 (ja) * 1999-04-01 2007-06-13 東燃ゼネラル石油株式会社 内燃機関用潤滑油組成物
US7332001B2 (en) * 2003-10-02 2008-02-19 Afton Chemical Corporation Method of enhancing the operation of diesel fuel combustion systems
US7615520B2 (en) * 2005-03-14 2009-11-10 Afton Chemical Corporation Additives and lubricant formulations for improved antioxidant properties
US7648949B2 (en) * 2005-01-27 2010-01-19 The Lubrizol Corporation Low phosphorus cobalt complex-containing engine oil lubricant
US20090029888A1 (en) * 2005-07-12 2009-01-29 Ramanathan Ravichandran Amine tungstates and lubricant compositions
WO2007009022A2 (fr) * 2005-07-12 2007-01-18 King Industries, Inc. Tungstates d'amine et compositions de graissage
US7772167B2 (en) * 2006-12-06 2010-08-10 Afton Chemical Corporation Titanium-containing lubricating oil composition
US7776800B2 (en) * 2005-12-09 2010-08-17 Afton Chemical Corporation Titanium-containing lubricating oil composition
GB2444612B (en) * 2005-12-09 2010-01-06 Afton Chemical Corp Titanium containing lubricating oil composition
US8278254B2 (en) * 2007-09-10 2012-10-02 Afton Chemical Corporation Additives and lubricant formulations having improved antiwear properties
US7897552B2 (en) * 2007-11-30 2011-03-01 Afton Chemical Corporation Additives and lubricant formulations for improved antioxidant properties
US8080501B2 (en) * 2008-02-29 2011-12-20 Exxonmobil Research And Engineering Company Green lubricant compositions
US8008237B2 (en) * 2008-06-18 2011-08-30 Afton Chemical Corporation Method for making a titanium-containing lubricant additive

Patent Citations (67)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2384577A (en) 1944-03-03 1945-09-11 Du Pont Esters
US2786866A (en) 1952-06-11 1957-03-26 American Cyanamid Co Esters of dithiocarbamic acids and a method for their preparation
US2710872A (en) 1954-04-12 1955-06-14 Universal Oil Prod Co Production of esters of dithiocarbamic acid
US2897152A (en) 1956-03-08 1959-07-28 Wakefield & Co Ltd C C Lubricating oils
US3219666A (en) 1959-03-30 1965-11-23 Derivatives of succinic acids and nitrogen compounds
US3509051A (en) 1964-08-07 1970-04-28 T R Vanderbilt Co Inc Lubricating compositions containing sulfurized oxymolybdenum dithiocarbamates
US3356702A (en) 1964-08-07 1967-12-05 Vanderbilt Co R T Molybdenum oxysulfide dithiocarbamates and processes for their preparation
US3565804A (en) 1965-08-23 1971-02-23 Chevron Res Lubricating oil additives
US3407222A (en) 1965-08-24 1968-10-22 American Cyanamid Co Preparation of 2-hydroxyalkyldithio carbamates from epoxides and amine salts of dithio-carbamic acid
US3697574A (en) 1965-10-22 1972-10-10 Standard Oil Co Boron derivatives of high molecular weight mannich condensation products
US3736357A (en) 1965-10-22 1973-05-29 Standard Oil Co High molecular weight mannich condensation products from two different alkyl-substituted hydroxy-aromatic compounds
US3794081A (en) 1972-05-05 1974-02-26 Smith Inland A O Fiber reinforced tubular article having abrasion resistant liner
US3867359A (en) 1973-11-16 1975-02-18 R F Vanderbilt Company Inc Process of vulcanizing neoprene by using certain 2-hydroxyalkyl N,N-dialkyldithiocarbamates as accelerators
US4029587A (en) 1975-06-23 1977-06-14 The Lubrizol Corporation Lubricants and functional fluids containing substituted sulfolanes as seal swelling agents
US4098705A (en) 1975-08-07 1978-07-04 Asahi Denka Kogyo K.K. Sulfur containing molybdenum dihydrocarbyldithiocarbamate compound
US4164473A (en) 1977-10-20 1979-08-14 Exxon Research & Engineering Co. Organo molybdenum friction reducing antiwear additives
US4178258A (en) 1978-05-18 1979-12-11 Edwin Cooper, Inc. Lubricating oil composition
US4234435A (en) 1979-02-23 1980-11-18 The Lubrizol Corporation Novel carboxylic acid acylating agents, derivatives thereof, concentrate and lubricant compositions containing the same, and processes for their preparation
US4285822A (en) 1979-06-28 1981-08-25 Chevron Research Company Process for preparing a sulfurized molybdenum-containing composition and lubricating oil containing the composition
US4263152A (en) 1979-06-28 1981-04-21 Chevron Research Company Process of preparing molybdenum complexes, the complexes so-produced and lubricants containing same
US4265773A (en) 1979-06-28 1981-05-05 Chevron Research Company Process of preparing molybdenum complexes, the complexes so-produced and lubricants containing same
US4272387A (en) 1979-06-28 1981-06-09 Chevron Research Company Process of preparing molybdenum complexes, the complexes so-produced and lubricants containing same
US4261843A (en) 1979-06-28 1981-04-14 Chevron Research Company Reaction product of acidic molybdenum compound with basic nitrogen compound and lubricants containing same
US4259195A (en) 1979-06-28 1981-03-31 Chevron Research Company Reaction product of acidic molybdenum compound with basic nitrogen compound and lubricants containing same
US4283295A (en) 1979-06-28 1981-08-11 Chevron Research Company Process for preparing a sulfurized molybdenum-containing composition and lubricating oil containing said composition
US4867890A (en) 1979-08-13 1989-09-19 Terence Colclough Lubricating oil compositions containing ashless dispersant, zinc dihydrocarbyldithiophosphate, metal detergent and a copper compound
US4266945A (en) 1979-11-23 1981-05-12 The Lubrizol Corporation Molybdenum-containing compositions and lubricants and fuels containing them
US4362633A (en) 1980-10-10 1982-12-07 Standard Oil Company (Indiana) Molybdenum-containing aminated sulfurized olefin lubricating oil additives
US4369119A (en) 1981-04-03 1983-01-18 Chevron Research Company Antioxidant combinations of molybdenum complexes and organic sulfur compounds for lubricating oils
US4402840A (en) 1981-07-01 1983-09-06 Chevron Research Company Antioxidant combinations of molybdenum complexes and organic sulfur compounds for lubricating oils
US4395343A (en) 1981-08-07 1983-07-26 Chevron Research Company Antioxidant combinations of sulfur containing molybdenum complexes and organic sulfur compounds
US4466901A (en) 1982-06-11 1984-08-21 Standard Oil Company (Indiana) Molybdenum-containing friction modifying additive for lubricating oils
US4692256A (en) 1985-06-12 1987-09-08 Asahi Denka Kogyo K.K. Molybdenum-containing lubricant composition
US4636322A (en) 1985-11-04 1987-01-13 Texaco Inc. Lubricating oil dispersant and viton seal additives
US4889647A (en) 1985-11-14 1989-12-26 R. T. Vanderbilt Company, Inc. Organic molybdenum complexes
US4758362A (en) 1986-03-18 1988-07-19 The Lubrizol Corporation Carbamate additives for low phosphorus or phosphorus free lubricating compositions
US4765918A (en) 1986-11-28 1988-08-23 Texaco Inc. Lubricant additive
EP0330522A2 (fr) 1988-02-26 1989-08-30 Exxon Chemical Patents Inc. Compositions démulsionnées d'huiles lubrifiantes
US4927552A (en) 1988-05-02 1990-05-22 Ethyl Petroleum Additives, Inc. Lubricating oil composition
US4876375A (en) 1988-05-02 1989-10-24 Ethyl Petroleum Additives, Inc. Norbornyl dithiocarbamates
US4885365A (en) 1988-05-20 1989-12-05 Ethyl Petroleum Additives, Inc. Dithiocarbanate lubricant compositions
US4957643A (en) 1988-05-20 1990-09-18 Ethyl Petroleum Additives, Inc. Lubricant compositions
US4978464A (en) 1989-09-07 1990-12-18 Exxon Research And Engineering Company Multi-function additive for lubricating oils
US4990271A (en) 1989-09-07 1991-02-05 Exxon Research And Engineering Company Antiwear, antioxidant and friction reducing additive for lubricating oils
US5633326A (en) 1989-12-13 1997-05-27 Exxon Chemical Patents Inc. Polyolefin-substituted amines grafted with poly(aromatic-N-monomers) for oleaginous compositions
US4995996A (en) 1989-12-14 1991-02-26 Exxon Research And Engineering Company Molybdenum sulfur antiwear and antioxidant lube additives
US4966719A (en) 1990-03-12 1990-10-30 Exxon Research & Engineering Company Multifunctional molybdenum and sulfur containing lube additives
US5137647A (en) 1991-12-09 1992-08-11 R. T. Vanderbilt Company, Inc. Organic molybdenum complexes
US5643859A (en) 1992-12-17 1997-07-01 Exxon Chemical Patents Inc. Derivatives of polyamines with one primary amine and secondary of tertiary amines
US5412130A (en) 1994-06-08 1995-05-02 R. T. Vanderbilt Company, Inc. Method for preparation of organic molybdenum compounds
US5627259A (en) 1994-06-17 1997-05-06 Exxon Chemical Patents Inc. Amidation of ester functionalized hydrocarbon polymers
US5936041A (en) 1994-06-17 1999-08-10 Exxon Chemical Patents Inc Dispersant additives and process
US5902776A (en) 1995-09-19 1999-05-11 The Lubrizol Corporation Additive compositions for lubricants and functional fluids
US5693598A (en) 1995-09-19 1997-12-02 The Lubrizol Corporation Low-viscosity lubricating oil and functional fluid compositions
US5851965A (en) 1995-12-01 1998-12-22 Chevron Chemical Company Dispersant compositions having polyalkylene succinimides
US5853434A (en) 1995-12-01 1998-12-29 Chevron Chemical Company Fuel compositions having polyalkylene succinimides and preparation thereof
US5792729A (en) 1996-08-20 1998-08-11 Chevron Chemical Corporation Dispersant terpolymers
US6232276B1 (en) 1996-12-13 2001-05-15 Infineum Usa L.P. Trinuclear molybdenum multifunctional additive for lubricating oils
US5789357A (en) 1997-01-10 1998-08-04 Uniroyal Chemical Company, Inc. Dithiocarbamyl carboxylic acids and their use as multifunctional additives for lubricating oils
US5686397A (en) 1997-02-03 1997-11-11 Uniroyal Chemical Company, Inc. Dithiocarbamate derivatives and lubricants containing same
US6117826A (en) 1998-09-08 2000-09-12 Uniroyal Chemical Company, Inc. Dithiocarbamyl derivatives useful as lubricant additives
US6103674A (en) 1999-03-15 2000-08-15 Uniroyal Chemical Company, Inc. Oil-soluble molybdenum multifunctional friction modifier additives for lubricant compositions
US6509303B1 (en) 2000-03-23 2003-01-21 Ethyl Corporation Oil soluble molybdenum additives from the reaction product of fatty oils and monosubstituted alkylene diamines
US6528463B1 (en) 2000-03-23 2003-03-04 Ethyl Corporation Oil soluble molybdenum compositions
US6797677B2 (en) 2002-05-30 2004-09-28 Afton Chemical Corporation Antioxidant combination for oxidation and deposit control in lubricants containing molybdenum and alkylated phenothiazine
US6599865B1 (en) 2002-07-12 2003-07-29 Ethyl Corporation Effective antioxidant combination for oxidation and deposit control in crankcase lubricants
US20040266630A1 (en) 2003-06-25 2004-12-30 The Lubrizol Corporation, A Corporation Of The State Of Ohio Novel additive composition that reduces soot and/or emissions from engines

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WO2019012447A1 (fr) * 2017-07-14 2019-01-17 Chevron Oronite Company Llc Compositions d'huile lubrifiante contenant du zirconium et procédé pour empêcher ou réduire le préallumage à faible vitesse dans des moteurs à allumage par étincelle à injection directe
CN111051479A (zh) * 2017-07-14 2020-04-21 雪佛龙奥伦耐有限责任公司 含锆的润滑油组合物以及用于防止或减少直喷式火花点火发动机中低速提前点火的方法
JP2020526634A (ja) * 2017-07-14 2020-08-31 シェブロン・オロナイト・カンパニー・エルエルシー ジルコニウムを含む潤滑油組成物および直接噴射火花点火式エンジンにおける低速早期着火を防止または低減する方法
EP4134414A1 (fr) * 2017-07-14 2023-02-15 Chevron U.S.A. Inc. Compositions d'huiles lubrifiantes contenant du zirconium et procédé pour empêcher ou réduire le pré-allumage à bas régime dans des moteurs à allumage commandé à injection directe

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