EP0092946A2 - Glycerol esters with oil-soluble copper compounds as fuel economy additives - Google Patents

Glycerol esters with oil-soluble copper compounds as fuel economy additives Download PDF

Info

Publication number
EP0092946A2
EP0092946A2 EP83302155A EP83302155A EP0092946A2 EP 0092946 A2 EP0092946 A2 EP 0092946A2 EP 83302155 A EP83302155 A EP 83302155A EP 83302155 A EP83302155 A EP 83302155A EP 0092946 A2 EP0092946 A2 EP 0092946A2
Authority
EP
European Patent Office
Prior art keywords
oil
fuel economy
copper
glycerol
composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP83302155A
Other languages
German (de)
French (fr)
Other versions
EP0092946B1 (en
EP0092946A3 (en
Inventor
Phillip William Brewster
Clinton Richard Smith
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ExxonMobil Technology and Engineering Co
Original Assignee
Exxon Research and Engineering Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Exxon Research and Engineering Co filed Critical Exxon Research and Engineering Co
Publication of EP0092946A2 publication Critical patent/EP0092946A2/en
Publication of EP0092946A3 publication Critical patent/EP0092946A3/en
Application granted granted Critical
Publication of EP0092946B1 publication Critical patent/EP0092946B1/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C10M129/04Hydroxy 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
    • 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
    • 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
    • C10M129/56Acids of unknown or incompletely defined constitution
    • C10M129/58Naphthenic 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
    • C10M129/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
    • C10M129/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
    • C10M129/68Esters
    • C10M129/76Esters containing free hydroxy or carboxyl 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
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • 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
    • C10M2205/026Butene
    • 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
    • C10M2205/06Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing conjugated dienes
    • 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
    • C10M2207/02Hydroxy 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • 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
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/027Neutral salts thereof
    • 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
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/028Overbased salts thereof
    • 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
    • C10M2207/09Metal enolates, i.e. keto-enol metal complexes
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • C10M2207/126Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids monocarboxylic
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/129Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/16Naphthenic acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/287Partial esters
    • 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
    • C10M2207/28Esters
    • C10M2207/287Partial esters
    • C10M2207/288Partial esters containing free carboxyl 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/287Partial esters
    • C10M2207/289Partial esters containing free hydroxy 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/08Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
    • C10M2209/084Acrylate; Methacrylate
    • 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/08Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
    • C10M2209/086Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type polycarboxylic, e.g. maleic acid
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/04Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic 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
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/064Di- and triaryl amines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/064Di- and triaryl amines
    • C10M2215/065Phenyl-Naphthyl amines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/26Amines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2217/00Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2217/02Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2217/022Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an amino group
    • C10M2217/023Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an amino group the amino group containing an ester 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
    • C10M2217/00Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2217/02Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2217/024Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an amido or imido group
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2217/00Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2217/02Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2217/028Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a nitrogen-containing hetero ring
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2217/00Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2217/04Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2217/046Polyamines, i.e. macromoleculars obtained by condensation of more than eleven amine monomers
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2217/00Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2217/06Macromolecular compounds obtained by functionalisation op polymers with a nitrogen 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
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/044Sulfonic acids, Derivatives thereof, e.g. neutral salts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/046Overbasedsulfonic acid salts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/06Thio-acids; Thiocyanates; Derivatives thereof
    • C10M2219/062Thio-acids; Thiocyanates; Derivatives thereof having carbon-to-sulfur double bonds
    • C10M2219/066Thiocarbamic type compounds
    • C10M2219/068Thiocarbamate metal salts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/08Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
    • C10M2219/087Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
    • 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
    • C10M2219/08Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
    • C10M2219/087Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
    • C10M2219/088Neutral salts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/08Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
    • C10M2219/087Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
    • C10M2219/089Overbased 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
    • 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
    • C10M2223/041Triaryl phosphates
    • 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
    • C10M2223/042Metal salts thereof
    • 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
    • C10M2227/06Organic compounds derived from inorganic acids or metal salts
    • C10M2227/061Esters derived from boron
    • 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
    • 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
    • C10N2010/02Groups 1 or 11

Definitions

  • British Application 2097813A published November 10, 1982, discloses the use of 0.05 to 0.2 wt% glycerol partial esters of C 16 -C 18 fatty acids as fuel economy additives.
  • the present invention is an improvement over said British application.
  • West German Application P-2949940 and P-2949910 of Chevron Research Company both published July 3, 1980, disclose the use of glycerol fatty esters as fuel economy additives. These references state that the addition of 0.25 to 2 weight percent, preferably 0.40 to 1.25 weight percent, of a fatty acid ester will offer a fuel economy credit of 2-3 percent in both gasoline and diesel engines. Glycerol oleic acid esters are preferred.
  • West German Application P-2949940 illustrates the preferred embodiment showing the use of the glycerol ester at the same treat level in combination with zinc dihydrocarbyl dithiophosphate additives.
  • U.S. Patent 4,304,678 discloses hydroxyl-containing esters including glycerol oleates as being effective friction modifiers only at levels of 1-4 wt% with no benefit observed at levels less than 1% by wt. in oil.
  • the present invention is based upon the discovery that very low levels of glycerol esters; that is, up to about 0.2 percent by weight, in combination with certain amounts of oil-soluble organic copper compounds, provide enhanced performance of these fuel economy lubricating oils. No benefit is obtainable in using relatively higher amounts and in some cases substantial debits in terms of formulation stability or adverse performance may occur.
  • U.S. Patent 3,933,659 shows a multi-component functional fluid, one component of which can be a polyol ester friction modifier or a fatty acid amide friction modifier.
  • the primary use disclosed in that reference is for automatic transmission fluids.
  • U.S. Patent 3,273,981 discloses antiwear additives comprising a mixture of dimer acids and a partial ester of a polyhydric alcohol, the additive being noted as improving lubricity as well as functioning in the anti-wear category.
  • U.S. Patent 3,112,271 discloses glycerol mono-oleate as an extreme pressure additive as does U.S. 3,112,269 and U.S. 3,041,284.
  • U.S. 2,493,483 discloses marine engine lubricants which contain a partial ester of glycerol or other polyol fatty acid esters in amounts of from 0.05 to 1 percent.
  • oil-soluble copper compounds at levels of about 5 to 500 parts per million (ppm) of copper by weight, based on the total weight of lubricating oil composition,as a highly effective antioxidant is a relatively recent development of additive technology and is disclosed in European Published Application No. 0024146, published on February 25, 1981.
  • fuel economy improving lubricating oil compositions for internal combustion engines which comprise an oil of lubricating viscosity and, as the fuel economy additive, a combination from 0.05 to 0.20 weight percent of a glycerol partial ester of a C 16 -C 18 fatty acid with from 5 to 500 ppm (parts per million) copper present in the form of an oil-soluble copper compound, preferably about 60 to 200 ppm copper being present, based upon the weight of the total composition, the copper compound also functioning as an antioxidant.
  • the lubricating oil compositions of the present invention comprise both straight grade and multigrade lubricating oil formulations for both gasoline and diesel (compression ignition) engines.
  • the lubricating oil compositions will contain those additive systems formulated to meet the viscosity requirements or other specifications as required for qualification as a gasoline engine or diesel lubricating oil.
  • a straight grade lubricating oil formulation will normally contain conventional amounts of an ashless dispersant, a normal or basic metal detergent, an anti-wear additive and an antioxidant and a multi-grade oil will contain, in addition to the foregoing, a viscosity index improver or viscosity modifier.
  • very small proportions of other special purpose additives such as pour depressants, rust inhibitors, anti-foamants and the like are conventionally blended into lubricating oil compositions.
  • the ester component of the fuel economy additive of the present invention is preferably a glycerol mono- or diester of a saturated or unsaturated C 16 -C 18 fatty acid, such as oleic or linoleic acid.
  • Optimum efficiency has been found to be at about the 0.1 to 0.2 weight percent level and use in the excess of this amount may even be detrimental to the overall performance of the lubricating oil composition.
  • Oil-soluble copper components useful herein include both cuprous or cupric compounds which are oil-soluble under normal blending conditions in the oil additive package. Particularly preferred are the copper salts of C 10 -C 22 fatty acids, such as stearic or palmitic acid, but copper salts of unsaturated acids, such as oleic acid, linoleic acid, naphthenic acid of 200-500 molecular weight or synthetic carboxylic acids are preferred.
  • the particularly preferred embodiment is copper (cupric) oleate when present in an amount to provide about 100 to 150 ppm copper in the lubricating oil composition.
  • Crankcase oil formulations to which the present invention relates are those which contain a major amount of lubricating oil and effective amounts of conventional additives in addition to the aforesaid fuel economy additive, the copper compound serving the dual function of being both an antioxidant and, in combination with the glycerol oleate, a fuel economy additive.
  • Percentages of additives as described herein are by weight based on the total weight of lubricating oil formulation unless otherwise indicated.
  • Detergents useful in the formulations include the normal, basic or overbased metal, that is, calcium, magnesium and so forth, salts of petroleum naphthenic acids, petroleum sulfonic acids, alkyl benzene sulfonic acids, alkyl phenols, alkylene-bis-phenol, oil-soluble fatty acids and the like.
  • the preferred materials are the normal or overbased calcium or magnesium phenates, sulfurized phenates and/or sulfonates, and these metal-containing detergent additives are typically used in amounts of from 1 to 3 wt % based on the total weight of lubricating oil compositions.
  • Suitable pour point depressants which are usually present in amounts of about 0.01 to 1 wt.%, include wax alkylated aromatic hydrocarbons, olefin polymers and copolymers, acrylate and methacrylate polymers and copolymers.
  • Anti-wear additives generally are the oil-soluble zinc dihydrocarbyl dithiophosphates having a least a total of 5 carbon atoms, the alkyl group being preferably C 2 -C S . These are typically present in amounts of from 0.01 to 5 wt. %, preferably 0.5 to 1.5 wt. %, in the lubricating oil.
  • Suitable conventional viscosity index improvers, or viscosity modifiers are the olefin polymers such as polybutene, ethylene-propylene copolymers, hydrogenated polymers and copolymers and terpolymers of styrene with isoprene and/or butadiene, polymers of alkyl acrylates or alkyl methacrylates, copolymers of alkylmethacrylates with N-vinyl pyrrolidone or dimethylaminoalkyl methacrylate, post-grafted polymers of ethylene-propylene with an active monomer, such as maleic anhydride, which may be further reacted with an alcohol or an alkylene polyamine, styrene-maleic anhydride polymers post- reacted with alcohols and amines and the like. These additives are used in amounts of about 1.5% to 15% by wt., depending on the exact viscosity specifications desired.
  • antioxidants include phenols, hindered phenols, bis-pheno1s, sulfurized phenols, catechol, alkylated and sulfurized alkylated catechols, diphenylamine, alkylated diphenylamines and phenyl-l-naphthylamines, alkyl and aryl borates, phosphites and phosphates, trialkyl and triaryl dithiophosphates and the like.
  • Suitable hydrocarbon base stocks are those mineral oils of lubricating viscosity as measured by ASTM D-455 of from about 2 to 40, preferably 5 to 20 centistokes at 99 0 C.
  • the reference oil used in this example was a formulated straight grade 20W30 crankcase mineral lubricating oil (corresponding to ASTM "HR" oil) to which was added 0.2 weight percent of a glycerol monooleate (GMO) fuel economy additive or 0.2 weight percent of a fuel economy additive being a mixture (GMO/GDO) of glycerol monooleate and glycerol dioleate in a weight ratio of 3 parts of GMO to 2 parts of GDO in said mixture.
  • the reference oil contained 2.10 wt % dispersant, 1.10 wt. % antioxidant, 1.00 wt. % basic metal detergent, 1. 95 wt.
  • results are expressed as a percentage fuel economy credit with respect to the referenced oil, as are all fuel economy credit results reported in the Examples.
  • Results at the 0.2 wt. % treat level for both GMO and the GMO/GDO mixture are set forth in Table I.
  • Example 1 The Laboratory Fuel Economy Test of Example 1 was repeated utilizing a 10W40 multigrade mineral oil containing 0.09 wt. % of the GMO/GDO mixture as the fuel economy additive.
  • the oil contained about 14% by wt. of a multifunctional dispersant viscosity index improver (acryloid 1155), 0.5% dispersant, 1.85% of basic metal detergent, 0.75 wt.% of anti-wear additive and 0.75% antioxidant.
  • Table III shows the fuel economy credits over the oil used as the reference in Example 1. Laboratory Fuel economy results were confirmed in the Proposed ASTM 5 Car Interim Fuel Economy Procedure which utilized the EPA car certification cycle in 5 automobiles having engine sizes of 2.3 liter, 2.8 liter, 3.7 liter, 3.8 liter and 5.0 liter. Five Car average fuel economy credit of 1.64% was obtained in one series of fuel economy tests.
  • Example 6 This will be demonstrated in Example 6.
  • Example 1-4 and 6 are presented here to illustrate these principles.
  • the LEFET test was carried out using an Oil * equivalent to the HR straight grade oil of Example 1 except that 0.3 wt. % of a 40 wt% solution of copper oleate in mineral oil, which is equivalent to 120 ppm copper was used in place of the anti- oxidant reported in Example 1.
  • the LEFET results for this test are below in Table IV:
  • oils containing both the oil-soluble organic copper compound and glycerol ester friction modifier would exhibit any complementary effect
  • different oils were formulated and tested in Ford 2.3 liter 4-cylinder engine.
  • the purpose of these tests was to evaluate the increase in fuel economy credits when the copper compound and the glycerol ester were combined over the credits obtained with these additives separately in the same engine.
  • Fuel economy credit values will vary among engines of differing sizes. This is due to the inherent differences in engine design and operating conditions. It is known therefore that the values for a 2.3 liter 4-cylinder engine will be lower than fuel economy credit values for a 5 liter 8-cylinder used in these examples.
  • balance is basestock mineral oil.
  • Oil D represents the advantage of this invention. Oils B, C, E show the maximum values one can expect to obtain based on the credits due only to the copper compound. Oil D, however, achieves a value of 0.9%. This result is not expected because it is known, as a general principle, that merely increasing the treatment level of a given fuel economy additive does not increase the credit obtained.
  • Oil G was a formulated lubricating oil having 4 wt% dispersant, 1 wt% overbased metal sulfonate, 1.5 wt% antioxidant and 2 wt% anti-wear additive.
  • Oil H was the same as Oil G , except for the inclusion of 0.1 wt% dimerized linoleic acid ester of diethylene glycol as disclosed in U.S. Patent 4, 105, 571.
  • Oil I was the same as Oil G except 0.2 wt% of the GMO/GDO ester was added.
  • Oil J was the same as Oil G except both 0.1 wt% of the dimerized linoleic acid ester and 0.2 wt% of the GMO/GDO were added. Fuel economy results for these four oils are shown below in Table V I .
  • Oil K contained 5.5 wt% dispersant, 1 wt% overbased metal sulfonate, 1.4 wt% anti-wear additive and 1 wt% anti-oxidant.
  • Oil L was the same as Oil K with .0.3 wt% of a 40 wt% solution of copper oleate (120 ppm copper) included and Oil M was the same as Oil L except 0.1 wt% of the GMO/GDO glycerol oleate was included.
  • Fuel economy credits are in Table VII below.

Abstract

Lubricating oil compositions are disclosed exhibiting improved fuel economy which contain 0.05 to 0.2 wt. % of a glycerol partial ester of a C16-C18 fatty acid and 5 to 500 ppm of copper in the form of an oil-soluble organic copper compound, the two components exhibiting a combined effect in improving fuel economy of internal combustion engines.

Description

  • This invention relates to lubricating oil compositions which exhibit marked improvements in fuel economy. More particularly, this invention relates to lubricating oil compositions which contain very minor proportions of a glycerol fatty acid ester fuel economy additive in combination with an oil-soluble organic copper compound.
  • It is a current objective of the industry to provide lubricating oil compositions which exhibit improvements in fuel savings in gasoline and diesel engine vehicles. To meet that current goal, a new category of additives commonly referred to as fuel economy additives are being developed which function primarily to increase the miles or kilometers obtained per unit volume of fuel. Since modern day lubricating oil compositions are complex formulations, such additives must be compatible with the other components of such compositions and should not adversely affect the numerous other functions of conventional lubricant additives such as dispersancy, viscosity stability, corrosion and oxidation inhibition, and the like.
  • Illustrative of recent patents reflecting developments in this field are U.S. Patents 4,201,684 and 4,208,293. These patents show the use of fatty acid amides and sulfurized amides as additives which have fuel economy benefits as demonstrated by friction reducing data.
  • The present invention concerns the use of glycerol fatty acid esters as such fuel economy additives, specifically glycerol esters of C16-C18 fatty acids in combination with oil-soluble copper organic compounds. There is prior art disclosing the use of each of these materials in lubricating oil compositions which is discussed hereinbelow.
  • British Application 2097813A, published November 10, 1982, discloses the use of 0.05 to 0.2 wt% glycerol partial esters of C16-C18 fatty acids as fuel economy additives. The present invention is an improvement over said British application.
  • West German Application P-2949940 and P-2949910 of Chevron Research Company, both published July 3, 1980, disclose the use of glycerol fatty esters as fuel economy additives. These references state that the addition of 0.25 to 2 weight percent, preferably 0.40 to 1.25 weight percent, of a fatty acid ester will offer a fuel economy credit of 2-3 percent in both gasoline and diesel engines. Glycerol oleic acid esters are preferred. West German Application P-2949940 illustrates the preferred embodiment showing the use of the glycerol ester at the same treat level in combination with zinc dihydrocarbyl dithiophosphate additives. Similarly U.S. Patent 4,304,678 discloses hydroxyl-containing esters including glycerol oleates as being effective friction modifiers only at levels of 1-4 wt% with no benefit observed at levels less than 1% by wt. in oil.
  • In contrast to the teachings of these references, the present invention is based upon the discovery that very low levels of glycerol esters; that is, up to about 0.2 percent by weight, in combination with certain amounts of oil-soluble organic copper compounds, provide enhanced performance of these fuel economy lubricating oils. No benefit is obtainable in using relatively higher amounts and in some cases substantial debits in terms of formulation stability or adverse performance may occur.
  • Another reference disclosing the use of polyol- carboxylic acid esters in lubricating oil compositions is U.S. Patent 3,933,659, which shows a multi-component functional fluid, one component of which can be a polyol ester friction modifier or a fatty acid amide friction modifier. The primary use disclosed in that reference is for automatic transmission fluids. U.S. Patent 3,273,981 discloses antiwear additives comprising a mixture of dimer acids and a partial ester of a polyhydric alcohol, the additive being noted as improving lubricity as well as functioning in the anti-wear category. U.S. Patent 3,112,271 discloses glycerol mono-oleate as an extreme pressure additive as does U.S. 3,112,269 and U.S. 3,041,284. U.S. 2,493,483 discloses marine engine lubricants which contain a partial ester of glycerol or other polyol fatty acid esters in amounts of from 0.05 to 1 percent.
  • Other references disclosing polyol esters of fatty acids are represented.by U.S. 2,788,326, which discloses these compounds as being useful in extreme pressure lubricants and U.S. Patent 2,527,889, which shows the same polyol esters, such as glycerol monooleate, being useful as anti-corrosion agents in turbine oils and diesel fuels.
  • The use of oil-soluble copper compounds at levels of about 5 to 500 parts per million (ppm) of copper by weight, based on the total weight of lubricating oil composition,as a highly effective antioxidant is a relatively recent development of additive technology and is disclosed in European Published Application No. 0024146, published on February 25, 1981.
  • The present invention is based on the discovery that these copper compounds, when used in an oil in combination with glycerol esters, e.g. oleates, act cooperatively with the glycerol ester in substantially increasing the fuel economy of the formulated oil. The cumulative effect observed would not be expected by adding the fuel economy credit obtained in oils which contain one or the other of the glycerol ester or copper compound. Data obtained therefore provide the basis for an unexpected additive effect upon fuel economy due to more effective lubrication of an internal combustion engine operated using the oils of the present invention.
  • The prior art also recognizes that copper components per se can be favorable friction reducing agents in certain circumstances. German Democratic Republic Patents 145,469 and 145,470 disclose the reduction of wear and friction in iron/iron and iron/bronze friction interfaces using polyol or mineral oil lubricants containing copper compounds such as copper naphthenate, copper octoate, copper stearate and reaction products of lubricants themselves with copper, copper oxide and copper salts of inorganic acids. These references indicate that the friction reduction is achieved by deposition on the substrate being lubricated of a film reaction layer of copper with adequate adhesion properties. It is recommended in these references that the concentration of the copper compound in the lubricant provide a copper content of 0.001 to 5 volume % relative to the lubricant. These references however did not evaluate lubricating oil compositions for internal combustion engines.
  • In accordance with the present invention, there are provided fuel economy improving lubricating oil compositions for internal combustion engines which comprise an oil of lubricating viscosity and, as the fuel economy additive, a combination from 0.05 to 0.20 weight percent of a glycerol partial ester of a C16-C18 fatty acid with from 5 to 500 ppm (parts per million) copper present in the form of an oil-soluble copper compound, preferably about 60 to 200 ppm copper being present, based upon the weight of the total composition, the copper compound also functioning as an antioxidant.
  • The lubricating oil compositions of the present invention comprise both straight grade and multigrade lubricating oil formulations for both gasoline and diesel (compression ignition) engines. Thus, in the practice of the present invention the lubricating oil compositions will contain those additive systems formulated to meet the viscosity requirements or other specifications as required for qualification as a gasoline engine or diesel lubricating oil. A straight grade lubricating oil formulation will normally contain conventional amounts of an ashless dispersant, a normal or basic metal detergent, an anti-wear additive and an antioxidant and a multi-grade oil will contain, in addition to the foregoing, a viscosity index improver or viscosity modifier. In addition to these principal additives, very small proportions of other special purpose additives, such as pour depressants, rust inhibitors, anti-foamants and the like are conventionally blended into lubricating oil compositions.
  • The ester component of the fuel economy additive of the present invention is preferably a glycerol mono- or diester of a saturated or unsaturated C16-C18 fatty acid, such as oleic or linoleic acid. Optimum efficiency has been found to be at about the 0.1 to 0.2 weight percent level and use in the excess of this amount may even be detrimental to the overall performance of the lubricating oil composition.
  • Oil-soluble copper components useful herein include both cuprous or cupric compounds which are oil-soluble under normal blending conditions in the oil additive package. Particularly preferred are the copper salts of C10-C22 fatty acids, such as stearic or palmitic acid, but copper salts of unsaturated acids, such as oleic acid, linoleic acid, naphthenic acid of 200-500 molecular weight or synthetic carboxylic acids are preferred. The particularly preferred embodiment is copper (cupric) oleate when present in an amount to provide about 100 to 150 ppm copper in the lubricating oil composition.
  • Other suitable copper compounds include the same as those disclosed in said European Published Application 0024146 and these include copper dithiocarbamates of the formula (RR'NCSS)nCu where n is 1 or 2 and R and R' are the same or different Cl-Cl8 hydrocarbyl radicals, preferably C2-C8 alkyl, copper sulphonates, copper phenates and acetyl acetonates as well as copper dihydrocarbyl dithiophosphate, the hydrocarbyl being C1-C18 and preferably C2-C8 alkyl, such as a hexyl or isooctyl.
  • Crankcase oil formulations to which the present invention relates are those which contain a major amount of lubricating oil and effective amounts of conventional additives in addition to the aforesaid fuel economy additive, the copper compound serving the dual function of being both an antioxidant and, in combination with the glycerol oleate, a fuel economy additive. Percentages of additives as described herein are by weight based on the total weight of lubricating oil formulation unless otherwise indicated.
  • These conventional additives comprise ashless dispersants typically nitrogen-containing dispersant additives which are oil-soluble salts, amides, imides and esters made from high molecular weight mono- or di-carboxylic acids and various amines having an amino or heterocyclic nitrogen with at least one amido or hydroxy group capable of salt, amide or ester formation. Preferred are the reaction products of polyolefin (C2-C5 olefin), such as polyisobutenyl, succinic anhydride with an alkylene polyamine such as tetraethylenepentamine. The polyisobutenyl portion has between 50 and 250 carbon atoms. The alkylene polyamines are those represented by the formula:
    NH2(CH2)n(NH(CH2)n)m-NH2
    where n is 2 to 3 and m is a number from 0 to 10. Mixtures of alkylene polyamines which approximate tetraethylenepentamine are commercially available materials. Dispersants are used generally in amounts of from about 0.1 to 10 wt.%, preferably in the range of about 0.5 to 5 wt %, based on the weight of the lubricating oil composition.
  • Detergents useful in the formulations include the normal, basic or overbased metal, that is, calcium, magnesium and so forth, salts of petroleum naphthenic acids, petroleum sulfonic acids, alkyl benzene sulfonic acids, alkyl phenols, alkylene-bis-phenol, oil-soluble fatty acids and the like. The preferred materials are the normal or overbased calcium or magnesium phenates, sulfurized phenates and/or sulfonates, and these metal-containing detergent additives are typically used in amounts of from 1 to 3 wt % based on the total weight of lubricating oil compositions.
  • Suitable pour point depressants, which are usually present in amounts of about 0.01 to 1 wt.%, include wax alkylated aromatic hydrocarbons, olefin polymers and copolymers, acrylate and methacrylate polymers and copolymers.
  • Anti-wear additives generally are the oil-soluble zinc dihydrocarbyl dithiophosphates having a least a total of 5 carbon atoms, the alkyl group being preferably C2-CS. These are typically present in amounts of from 0.01 to 5 wt. %, preferably 0.5 to 1.5 wt. %, in the lubricating oil.
  • Suitable conventional viscosity index improvers, or viscosity modifiers, are the olefin polymers such as polybutene, ethylene-propylene copolymers, hydrogenated polymers and copolymers and terpolymers of styrene with isoprene and/or butadiene, polymers of alkyl acrylates or alkyl methacrylates, copolymers of alkylmethacrylates with N-vinyl pyrrolidone or dimethylaminoalkyl methacrylate, post-grafted polymers of ethylene-propylene with an active monomer, such as maleic anhydride, which may be further reacted with an alcohol or an alkylene polyamine, styrene-maleic anhydride polymers post- reacted with alcohols and amines and the like. These additives are used in amounts of about 1.5% to 15% by wt., depending on the exact viscosity specifications desired.
  • Conventionally used antioxidants include phenols, hindered phenols, bis-pheno1s, sulfurized phenols, catechol, alkylated and sulfurized alkylated catechols, diphenylamine, alkylated diphenylamines and phenyl-l-naphthylamines, alkyl and aryl borates, phosphites and phosphates, trialkyl and triaryl dithiophosphates and the like.
  • Suitable hydrocarbon base stocks are those mineral oils of lubricating viscosity as measured by ASTM D-455 of from about 2 to 40, preferably 5 to 20 centistokes at 990C.
  • These conventional additives are used in amounts normally necessary to provide their attendant functions in a formulated crankcase lubricating oil composition. Very small proportions of additional special purpose additives, such as anti-foam agents or rust inhibitors, may also be present in a fully formulated lubricating oil composition.
  • The invention is further illustrated by the following Examples.
  • EXAMPLE 1
  • The reference oil used in this example was a formulated straight grade 20W30 crankcase mineral lubricating oil (corresponding to ASTM "HR" oil) to which was added 0.2 weight percent of a glycerol monooleate (GMO) fuel economy additive or 0.2 weight percent of a fuel economy additive being a mixture (GMO/GDO) of glycerol monooleate and glycerol dioleate in a weight ratio of 3 parts of GMO to 2 parts of GDO in said mixture. The reference oil contained 2.10 wt % dispersant, 1.10 wt. % antioxidant, 1.00 wt. % basic metal detergent, 1. 95 wt. % anti- wear additive, 0.21 wt % pour depressant and 0.001 wt. % anti-foam agent. This type of reference oil, which is generally accepted by the industry for establishing fuel economy data, provides a reproducible baseline against which fuel economy credits may be measured and is considered to provide test results which accurately reflect the effect of a given fuel economy additive.
  • Fuel economy was evaluated using the Laboratory Engine Fuel Economy Test (LEFET) summarized below:
    • The fuel economy test used is a fired engine procedure. The engine is a 5.0 liter, V-8 Chevrolet engine coupled to a water cooled electric dynamometer. The engine is run with a dry sump by the use of external oil pumps. One pump supplies oil to the oil gallery from an external sump and a second pump scavenges the sump and returns the oil to the external sump. The conditions that the engine runs at are as follows:
      Figure imgb0001
  • The results are expressed as a percentage fuel economy credit with respect to the referenced oil, as are all fuel economy credit results reported in the Examples. Results at the 0.2 wt. % treat level for both GMO and the GMO/GDO mixture are set forth in Table I.
    Figure imgb0002
  • EXAMPLE 2
    • (a) Comparative evaluations utilizing increased amounts of the GMO/GDO mixture, that is, at the 0.3 weight percent and 0.5 weight percent levels showed no increase in fuel economy credit for treatment at these levels and in some cases, an adverse effect on fuel economy credits or other lubricating oil performance criteria, such as increased piston deposit formation tendencies or poor results in bearing corrosion tests.
    • (b) Coefficient of friction (CF) testing using a Roxana Four-ball wear tester in acordance with the procedure described in ASTM D2266-67 at 110°C, 2.5 RPM at both 15 kg and 3 kg was carried out with a formulated mineral oil (Base oil) containing conventional amounts of dispersant (2.12 %), basic metal sulfonate (1.02%), antioxidant (0.72%), anti-wear additive (1.96%) and viscosity index improver (only present at 8.7 wt. % in test oils 5 and 6 to evaluate compatibility) to which was added varying amounts of the GDO/GMO mixture. The results in Table II below show essentially no additional friction reducing benefit at levels in excess of 0.2 wt. % and, at 0.9 wt. % in the test, potential instability or incompatibility was observed since the samples appeared hazy.
      Figure imgb0003
    EXAMPLE 3
  • (a) The Laboratory Fuel Economy Test of Example 1 was repeated utilizing a 10W40 multigrade mineral oil containing 0.09 wt. % of the GMO/GDO mixture as the fuel economy additive. The oil contained about 14% by wt. of a multifunctional dispersant viscosity index improver (acryloid 1155), 0.5% dispersant, 1.85% of basic metal detergent, 0.75 wt.% of anti-wear additive and 0.75% antioxidant.
  • Table III shows the fuel economy credits over the oil used as the reference in Example 1.
    Figure imgb0004
    Laboratory Fuel Economy results were confirmed in the Proposed ASTM 5 Car Interim Fuel Economy Procedure which utilized the EPA car certification cycle in 5 automobiles having engine sizes of 2.3 liter, 2.8 liter, 3.7 liter, 3.8 liter and 5.0 liter. Five Car average fuel economy credit of 1.64% was obtained in one series of fuel economy tests.
  • Based upon these results one would expect that the fuel economy credits attributed to a glycerol mono-oleate to be non-cumulative when the treatment level is increased above the range of about 0.1 wt. % to 0.2 wt. % and the inventors hereof have found this principle is generally true in fuel economy additives technology, i.e., increasing the amount of friction modifier additive does not result in a concomitant straight line proportional increase in the observed fuel economy. For example, combining the glycerol oleate mixed esters described above with a known fuel economy additive such as a dimerized linoleic acid ester as described in U.S. Patent 4,105,571 has been found to offer no better fuel economy than when either compound is used alone. This will be demonstrated in Example 6. Thus, as a general rule increasing the treat level of the friction modifier itself or increasing the treat level by adding another friction modifier known to have fuel economy benefits has not heretofore been found to offer a fuel economy improvement. Examples 1-4 and 6 are presented here to illustrate these principles.
  • EXAMPLE 4
  • Evaluation of Copper Compounds for Fuel Economy
  • The LEFET test was carried out using an Oil* equivalent to the HR straight grade oil of Example 1 except that 0.3 wt. % of a 40 wt% solution of copper oleate in mineral oil, which is equivalent to 120 ppm copper was used in place of the anti- oxidant reported in Example 1. The LEFET results for this test are below in Table IV:
    Figure imgb0005
  • This example establishes that copper does provide a significant fuel economy credit in addition to its antioxidant effectiveness.
  • The foregoing examples, carried out in fired engine tests using a 5.0 liter 8-cylinder engine demonstrate that the oil-soluble organic copper compounds offer a beneficial fuel economy credit and that the glycerol ester offers a fuel economy credit which does not increase to any significant degree above the 0.2 wt. % treat level.
  • EXAMPLE 5 - Evaluation of Combination of Copper Compound and Glycerol Ester
  • To determine if oils containing both the oil-soluble organic copper compound and glycerol ester friction modifier would exhibit any complementary effect, different oils were formulated and tested in Ford 2.3 liter 4-cylinder engine. The purpose of these tests was to evaluate the increase in fuel economy credits when the copper compound and the glycerol ester were combined over the credits obtained with these additives separately in the same engine. Fuel economy credit values will vary among engines of differing sizes. This is due to the inherent differences in engine design and operating conditions. It is known therefore that the values for a 2.3 liter 4-cylinder engine will be lower than fuel economy credit values for a 5 liter 8-cylinder used in these examples.
  • The additive content in weight percent of the oils evaluated is given below, balance is basestock mineral oil.
    Figure imgb0006
  • Fuel economy results for these oils are given in Table V below. Percentage credits are calculated again with respect to the same reference oil used in Example 1.
    Figure imgb0007
  • Oil D represents the advantage of this invention. Oils B, C, E show the maximum values one can expect to obtain based on the credits due only to the copper compound. Oil D, however, achieves a value of 0.9%. This result is not expected because it is known, as a general principle, that merely increasing the treatment level of a given fuel economy additive does not increase the credit obtained.
  • EXAMPLE 6
  • To demonstrate the principle that fuel economy additives, when combined together, cannot be expected to have a combined effect. The following oils G, H, I and J were evaluated for fuel economy in the 5.0 L engine using the same LEFET procedure of Example I. Oil G was a formulated lubricating oil having 4 wt% dispersant, 1 wt% overbased metal sulfonate, 1.5 wt% antioxidant and 2 wt% anti-wear additive. Oil H was the same as Oil G, except for the inclusion of 0.1 wt% dimerized linoleic acid ester of diethylene glycol as disclosed in U.S. Patent 4, 105, 571. Oil I was the same as Oil G except 0.2 wt% of the GMO/GDO ester was added. Oil J was the same as Oil G except both 0.1 wt% of the dimerized linoleic acid ester and 0.2 wt% of the GMO/GDO were added. Fuel economy results for these four oils are shown below in Table VI.
    Figure imgb0008
  • EXAMPLE 7
  • The positive effect on fuel economy attributable to use of the two component fuel economy additive of this invention is further demonstrated by LEFET results in the 5.0 L engine and these data confirm the results shown above in Example 5. Here Oil K contained 5.5 wt% dispersant, 1 wt% overbased metal sulfonate, 1.4 wt% anti-wear additive and 1 wt% anti-oxidant. Oil L was the same as Oil K with .0.3 wt% of a 40 wt% solution of copper oleate (120 ppm copper) included and Oil M was the same as Oil L except 0.1 wt% of the GMO/GDO glycerol oleate was included. Fuel economy credits are in Table VII below.
    Figure imgb0009

Claims (11)

1. A lubricating oil composition comprising a major amount of an oil of a lubricating viscosity which has incorporated therein (a) from about 0.05 to about 0.20 weight percent of a glycerol partial ester or mixtures thereof of a C16-C18 fatty acid, and (b) about 5 to 500 ppm of copper in the form of an oil-soluble organic copper compound, said (a) and (b) components exhibiting a combined effect improving the fuel economy of an internal combustion engine.
2. The composition of claim 1 wherein the fatty acid is oleic acid.
3. The composition of claim 1 wherein said partial ester is a mixture of glycerol monooleate and glycerol dioleate.
4. The composition of claims 1-3 wherein there is present 0.1 to 0.2 weight percent of said partial ester.
5. The composition of claims 1-4 wherein said lubricating oil composition contains an ashless dispersant, a metal detergent additive and a zinc dihydrocarbyl dithiophosphate anti-wear additive in conventional amounts to provide their normal attendant functions.
6. The composition of claim 5 wherein said lubricating oil composition contains a viscosity index improver.
7. The composition of claims 1-6 where said copper compound is copper oleate.
8. The composition of claims 1-7 where there is present 60 to 200 ppm of copper.
9. A method of improving the fuel economy of an internal combustion engine by lubricating the internal portion thereof with a lubricating oil composition containing (a) 0.05 to 0.2 wt % of a glycerol partial ester of a C16-C18 fatty acid or mixtures thereof and (b) about 5 to 500 ppm of copper in the form of an oil-soluble organic copper compound, said (a) and (b) components exhibiting a combined effect in improving the fuel economy of said engine.
10. The method of claim 9 wherein said (a) component is a mixture of glycerol monooleate and glycerol dioleate present in an amount of from 0.1 to 0.2 wt %, and said (b) component is copper oleate present in an amount to provide 60 to 200 ppm copper.
11. The use as an additive for lubricating oil of a mixture of (A) a glycerol partial ester or mixtures thereof of a C15-C18 fatty acid, and (B) an oil-soluble organic copper compound.
EP83302155A 1982-04-22 1983-04-15 Glycerol esters with oil-soluble copper compounds as fuel economy additives Expired EP0092946B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US37100882A 1982-04-22 1982-04-22
US371008 1982-04-22

Publications (3)

Publication Number Publication Date
EP0092946A2 true EP0092946A2 (en) 1983-11-02
EP0092946A3 EP0092946A3 (en) 1985-08-14
EP0092946B1 EP0092946B1 (en) 1988-03-16

Family

ID=23462117

Family Applications (1)

Application Number Title Priority Date Filing Date
EP83302155A Expired EP0092946B1 (en) 1982-04-22 1983-04-15 Glycerol esters with oil-soluble copper compounds as fuel economy additives

Country Status (4)

Country Link
EP (1) EP0092946B1 (en)
JP (1) JPS58191795A (en)
CA (1) CA1205451A (en)
DE (1) DE3376016D1 (en)

Cited By (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2505355A1 (en) * 1981-05-06 1982-11-12 Exxon Research Engineering Co LUBRICATING OIL COMPOSITION CONTAINING A PARTIAL GLYCEROL ESTER
EP0260863A2 (en) * 1986-09-15 1988-03-23 Exxon Research And Engineering Company Lubricating oil
EP0280579A2 (en) * 1987-02-27 1988-08-31 Exxon Chemical Patents Inc. Low phosphorus/low zinc lubricants
EP0294045A2 (en) * 1987-05-11 1988-12-07 Exxon Chemical Patents Inc. Amine compatibility aids in lubricating oil compositions
FR2634780A1 (en) * 1988-08-01 1990-02-02 Lubrizol Corp LUBRICATING OIL AND CONCENTRATE COMPOSITION FOR PREPARATION CONTAINING CARBOXYLIC DERIVATIVE COMPOSITION, ESTER AND DIHYDROCARBYLDITHIOPHOSPHORIC ACID METAL SALT
US4938881A (en) * 1988-08-01 1990-07-03 The Lubrizol Corporation Lubricating oil compositions and concentrates
US4952328A (en) * 1988-05-27 1990-08-28 The Lubrizol Corporation Lubricating oil compositions
US4956108A (en) * 1987-07-29 1990-09-11 Mobil Oil Corporation Copper salts of thiodipropionic acid derivatives as antioxidant additives process of making the same and fuel composition thereof
US4957651A (en) * 1988-01-15 1990-09-18 The Lubrizol Corporation Mixtures of partial fatty acid esters of polyhydric alcohols and sulfurized compositions, and use as lubricant additives
US4981602A (en) * 1988-06-13 1991-01-01 The Lubrizol Corporation Lubricating oil compositions and concentrates
US5013467A (en) * 1987-09-16 1991-05-07 Exxon Chemical Patents Inc. Novel oleaginous composition additives for improved rust inhibition
US5021173A (en) * 1988-02-26 1991-06-04 Exxon Chemical Patents, Inc. Friction modified oleaginous concentrates of improved stability
US5049290A (en) * 1987-05-11 1991-09-17 Exxon Chemical Patents Inc. Amine compatibility aids in lubricating oil compositions
US5102566A (en) * 1987-10-02 1992-04-07 Exxon Chemical Patents Inc. Low ash lubricant compositions for internal combustion engines (pt-727)
US5141657A (en) * 1987-10-02 1992-08-25 Exxon Chemical Patents Inc. Lubricant compositions for internal combustion engines
US5244591A (en) * 1992-03-23 1993-09-14 Chevron Research And Technology Company Lubricating oil compositions for internal combustion engines having silver bearing parts
US5320765A (en) * 1987-10-02 1994-06-14 Exxon Chemical Patents Inc. Low ash lubricant compositions for internal combustion engines
EP0652279A1 (en) * 1993-06-07 1995-05-10 Ethyl Corporation Fuel economy and oxidation inhibition in lubricant compositions for internal combustion engines
US6254849B1 (en) * 1999-07-28 2001-07-03 Chevron U.S.A. Inc. Zeolite SSZ-52
WO2001059037A2 (en) * 2000-02-14 2001-08-16 Exxonmobil Research And Engineering Company Lubricating oils having improved fuel economy retention properties
EP1925655A1 (en) 2006-11-22 2008-05-28 Infineum International Limited Lubricating oil compositions
EP2161326A1 (en) 2008-09-05 2010-03-10 Infineum International Limited Lubricating oil compositions
EP2390306A1 (en) 2009-12-01 2011-11-30 Infineum International Limited A lubricating oil composition
WO2011161406A1 (en) 2010-06-25 2011-12-29 Castrol Limited Uses and compositions
US9127232B2 (en) 2010-10-26 2015-09-08 Castrol Limited Non-aqueous lubricant and fuel compositions comprising fatty acid esters of hydroxy-carboxylic acids, and uses thereof
EP3115443A1 (en) 2015-07-07 2017-01-11 Ab Nanol Technologies Oy Organometallic salt composition, a method for its preparation and a lubricant additive composition
EP3252130A1 (en) 2016-06-03 2017-12-06 Infineum International Limited Additive package and lubricating oil composition
WO2020089212A1 (en) 2018-10-29 2020-05-07 Castrol Limited Lubricant compositions

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4822473B2 (en) 2001-04-02 2011-11-24 東燃ゼネラル石油株式会社 Lubricating oil composition for internal combustion engines
US6892531B2 (en) * 2003-04-02 2005-05-17 Julius J. Rim System for and methods of operating diesel engines to reduce harmful exhaust emissions and to improve engine lubrication
JP6027578B2 (en) * 2013-08-30 2016-11-16 良光 長井 Lubrication promoting liquid
CN107964441A (en) * 2017-10-19 2018-04-27 山东源根石油化工有限公司 A kind of organic copper antioxidant and the diesel engine oil containing the organic copper antioxidant

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2911367A (en) * 1957-07-01 1959-11-03 Gulf Oil Corp Mineral lubricating oil composition
EP0024146A1 (en) * 1979-08-13 1981-02-25 Exxon Research And Engineering Company Improved lubricating compositions
GB2097813A (en) * 1981-05-06 1982-11-10 Exxon Research Engineering Co Glycerol esters in lubricating oils as fuel economy additives

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1137463A (en) * 1978-12-18 1982-12-14 Thomas V. Liston Mileage-improving lubricating oil

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2911367A (en) * 1957-07-01 1959-11-03 Gulf Oil Corp Mineral lubricating oil composition
EP0024146A1 (en) * 1979-08-13 1981-02-25 Exxon Research And Engineering Company Improved lubricating compositions
GB2097813A (en) * 1981-05-06 1982-11-10 Exxon Research Engineering Co Glycerol esters in lubricating oils as fuel economy additives

Cited By (43)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2505355A1 (en) * 1981-05-06 1982-11-12 Exxon Research Engineering Co LUBRICATING OIL COMPOSITION CONTAINING A PARTIAL GLYCEROL ESTER
EP0260863A2 (en) * 1986-09-15 1988-03-23 Exxon Research And Engineering Company Lubricating oil
EP0260863A3 (en) * 1986-09-15 1989-02-15 Exxon Research And Engineering Company Lubricating oil
EP0280579A3 (en) * 1987-02-27 1989-03-15 Exxon Chemical Patents Inc. Low phosphorus/low zinc lubricants
EP0280579A2 (en) * 1987-02-27 1988-08-31 Exxon Chemical Patents Inc. Low phosphorus/low zinc lubricants
US4915857A (en) * 1987-05-11 1990-04-10 Exxon Chemical Patents Inc. Amine compatibility aids in lubricating oil compositions
US5049290A (en) * 1987-05-11 1991-09-17 Exxon Chemical Patents Inc. Amine compatibility aids in lubricating oil compositions
EP0294045A3 (en) * 1987-05-11 1989-03-22 Exxon Chemical Patents Inc. Amine compatibility aids in lubricating oil compositions
EP0294045A2 (en) * 1987-05-11 1988-12-07 Exxon Chemical Patents Inc. Amine compatibility aids in lubricating oil compositions
US4956108A (en) * 1987-07-29 1990-09-11 Mobil Oil Corporation Copper salts of thiodipropionic acid derivatives as antioxidant additives process of making the same and fuel composition thereof
US5013467A (en) * 1987-09-16 1991-05-07 Exxon Chemical Patents Inc. Novel oleaginous composition additives for improved rust inhibition
US5102566A (en) * 1987-10-02 1992-04-07 Exxon Chemical Patents Inc. Low ash lubricant compositions for internal combustion engines (pt-727)
US5141657A (en) * 1987-10-02 1992-08-25 Exxon Chemical Patents Inc. Lubricant compositions for internal combustion engines
US5320765A (en) * 1987-10-02 1994-06-14 Exxon Chemical Patents Inc. Low ash lubricant compositions for internal combustion engines
US4957651A (en) * 1988-01-15 1990-09-18 The Lubrizol Corporation Mixtures of partial fatty acid esters of polyhydric alcohols and sulfurized compositions, and use as lubricant additives
US5282991A (en) * 1988-02-26 1994-02-01 Exxon Chemical Patents Inc. Friction modified oleaginous concentrates of improved stability
US5021173A (en) * 1988-02-26 1991-06-04 Exxon Chemical Patents, Inc. Friction modified oleaginous concentrates of improved stability
US4952328A (en) * 1988-05-27 1990-08-28 The Lubrizol Corporation Lubricating oil compositions
US4981602A (en) * 1988-06-13 1991-01-01 The Lubrizol Corporation Lubricating oil compositions and concentrates
US4938881A (en) * 1988-08-01 1990-07-03 The Lubrizol Corporation Lubricating oil compositions and concentrates
EP0389573A1 (en) * 1988-08-01 1990-10-03 Lubrizol Corp Lubricating oil compositions and concentrates.
US4957649A (en) * 1988-08-01 1990-09-18 The Lubrizol Corporation Lubricating oil compositions and concentrates
BE1001977A3 (en) * 1988-08-01 1990-05-02 Lubrizol Corp LUBRICATING OIL COMPOSITIONS.
FR2634780A1 (en) * 1988-08-01 1990-02-02 Lubrizol Corp LUBRICATING OIL AND CONCENTRATE COMPOSITION FOR PREPARATION CONTAINING CARBOXYLIC DERIVATIVE COMPOSITION, ESTER AND DIHYDROCARBYLDITHIOPHOSPHORIC ACID METAL SALT
EP0389573B1 (en) * 1988-08-01 1995-01-11 The Lubrizol Corporation Lubricating oil compositions and concentrates
US5244591A (en) * 1992-03-23 1993-09-14 Chevron Research And Technology Company Lubricating oil compositions for internal combustion engines having silver bearing parts
EP0652279A1 (en) * 1993-06-07 1995-05-10 Ethyl Corporation Fuel economy and oxidation inhibition in lubricant compositions for internal combustion engines
US6379531B2 (en) * 1999-07-28 2002-04-30 Chevron U.S.A. Inc. Zeolite SSZ-52
US6254849B1 (en) * 1999-07-28 2001-07-03 Chevron U.S.A. Inc. Zeolite SSZ-52
WO2001059037A2 (en) * 2000-02-14 2001-08-16 Exxonmobil Research And Engineering Company Lubricating oils having improved fuel economy retention properties
WO2001059037A3 (en) * 2000-02-14 2002-01-24 Exxonmobil Res & Eng Co Lubricating oils having improved fuel economy retention properties
EP1925655A1 (en) 2006-11-22 2008-05-28 Infineum International Limited Lubricating oil compositions
EP2161326A1 (en) 2008-09-05 2010-03-10 Infineum International Limited Lubricating oil compositions
EP2390306A1 (en) 2009-12-01 2011-11-30 Infineum International Limited A lubricating oil composition
WO2011161406A1 (en) 2010-06-25 2011-12-29 Castrol Limited Uses and compositions
US9080120B2 (en) 2010-06-25 2015-07-14 Castrol Limited Uses and compositions
US9127232B2 (en) 2010-10-26 2015-09-08 Castrol Limited Non-aqueous lubricant and fuel compositions comprising fatty acid esters of hydroxy-carboxylic acids, and uses thereof
US9828564B2 (en) 2010-10-26 2017-11-28 Castrol Limited Non-aqueous lubricant and fuel compositions comprising fatty acid esters of hydroxy-carboxylic acids, and uses thereof
EP3115443A1 (en) 2015-07-07 2017-01-11 Ab Nanol Technologies Oy Organometallic salt composition, a method for its preparation and a lubricant additive composition
WO2017005967A1 (en) 2015-07-07 2017-01-12 Ab Nanol Technologies Oy Organometallic salt composition, a method for its preparation and a lubricant additive composition
US10618865B2 (en) 2015-07-07 2020-04-14 Ab Nanol Technologies Oy Organometallic salt composition, a method for its preparation and a lubricant additive composition
EP3252130A1 (en) 2016-06-03 2017-12-06 Infineum International Limited Additive package and lubricating oil composition
WO2020089212A1 (en) 2018-10-29 2020-05-07 Castrol Limited Lubricant compositions

Also Published As

Publication number Publication date
EP0092946B1 (en) 1988-03-16
DE3376016D1 (en) 1988-04-21
JPH0377837B2 (en) 1991-12-11
JPS58191795A (en) 1983-11-09
EP0092946A3 (en) 1985-08-14
CA1205451A (en) 1986-06-03

Similar Documents

Publication Publication Date Title
EP0092946B1 (en) Glycerol esters with oil-soluble copper compounds as fuel economy additives
US4683069A (en) Glycerol esters as fuel economy additives
US4686054A (en) Succinimide lubricating oil dispersant
AU609990B2 (en) Lubricating oil compositions
US5629272A (en) Low phosphorous engine oil compositions and additive compositions
EP0814148B1 (en) Low phosphorous engine oil compositions and additive compositions
CN101679903B (en) Lubricant composition for combustion engine containing dispersant additve and polymer dispersant viscosity index improver
JP3993901B2 (en) Lubricating oil composition
US5114603A (en) Friction reducing lubricating oil composition
CA1190216A (en) Succinimide lubricating oil dispersant
CA2549269C (en) Crankcase lubricating oil composition for protection of silver bearings in locomotive diesel engines
US4406803A (en) Method for improving fuel economy of internal combustion engines
CA1174660A (en) Glycerol esters as fuel economy additives
Bardasz et al. Additives for crankcase lubricant applications
JP4191795B2 (en) Crankcase lubricant for modern heavy duty diesel and gasoline fuel engines
US4800032A (en) Aliphatic hydrocarbon substituted aromatic hydrocarbons to control black sludge in lubricants
US4228020A (en) Lubricating oil composition
US5866520A (en) Lubricant composition suitable for direct fuel injected, crankcase-scavenged two-stroke cycle engines
US4356097A (en) Alkylphosphonate lubricating oil
EP0588561A1 (en) Low phosphorous engine oil compositions and additive compositions
CA2420248A1 (en) Low phosphorus lubricating oil composition
US4246125A (en) Lubricating oil and fuel composition
JPH0148319B2 (en)
JPH0570786A (en) Lubricating oil composition for alcohol engine
Castrol Additives for Crankcase Lubricant i lications

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19830428

AK Designated contracting states

Designated state(s): BE DE FR GB IT NL SE

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Designated state(s): BE DE FR GB IT NL SE

17Q First examination report despatched

Effective date: 19860731

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): BE DE FR GB IT NL SE

ITF It: translation for a ep patent filed

Owner name: ING. C. GREGORJ S.P.A.

REF Corresponds to:

Ref document number: 3376016

Country of ref document: DE

Date of ref document: 19880421

ET Fr: translation filed
PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
ITTA It: last paid annual fee
EAL Se: european patent in force in sweden

Ref document number: 83302155.3

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: SE

Payment date: 19960409

Year of fee payment: 14

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 19970314

Year of fee payment: 15

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 19970322

Year of fee payment: 15

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Effective date: 19970416

EUG Se: european patent has lapsed

Ref document number: 83302155.3

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19981101

NLV4 Nl: lapsed or anulled due to non-payment of the annual fee

Effective date: 19981101

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19990202

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: BE

Payment date: 20000329

Year of fee payment: 18

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20010312

Year of fee payment: 19

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20010319

Year of fee payment: 19

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20010430

BERE Be: lapsed

Owner name: EXXON RESEARCH AND ENGINEERING CY

Effective date: 20010430

REG Reference to a national code

Ref country code: GB

Ref legal event code: IF02

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20020415

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20020415

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20021231

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST