EP1692249B1 - Composition lubrifiante contenant de dispersants succinimide - Google Patents

Composition lubrifiante contenant de dispersants succinimide Download PDF

Info

Publication number
EP1692249B1
EP1692249B1 EP04813239A EP04813239A EP1692249B1 EP 1692249 B1 EP1692249 B1 EP 1692249B1 EP 04813239 A EP04813239 A EP 04813239A EP 04813239 A EP04813239 A EP 04813239A EP 1692249 B1 EP1692249 B1 EP 1692249B1
Authority
EP
European Patent Office
Prior art keywords
composition
dispersant
less
detergent
oil
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Not-in-force
Application number
EP04813239A
Other languages
German (de)
English (en)
Other versions
EP1692249A2 (fr
Inventor
R. Ian Wilby
Douglas M. Barr
Rodney J. Mcatee
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.)
Lubrizol Corp
Original Assignee
Lubrizol Corp
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 Lubrizol Corp filed Critical Lubrizol Corp
Priority to EP10152942A priority Critical patent/EP2184338A3/fr
Publication of EP1692249A2 publication Critical patent/EP1692249A2/fr
Application granted granted Critical
Publication of EP1692249B1 publication Critical patent/EP1692249B1/fr
Not-in-force legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M167/00—Lubricating compositions characterised by the additive being a mixture of a macromolecular compound, a non-macromolecular compound and a compound of unknown or incompletely defined constitution, each of these compounds being essential
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M163/00—Lubricating 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
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/022—Ethene
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/024—Propene
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/04—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing aromatic monomers, e.g. styrene
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02—Hydroxy compounds
    • C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02—Hydroxy compounds
    • C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/027—Neutral salts thereof
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02—Hydroxy compounds
    • C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/028—Overbased salts thereof
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10—Carboxylix acids; Neutral salts thereof
    • C10M2207/14—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/144—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings containing hydroxy groups
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/26—Overbased carboxylic acid salts
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/26—Overbased carboxylic acid salts
    • C10M2207/262—Overbased carboxylic acid salts derived from hydroxy substituted aromatic acids, e.g. salicylates
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/101—Condensation polymers of aldehydes or ketones and phenols, e.g. Also polyoxyalkylene ether derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/28—Amides; Imides
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/046—Overbasedsulfonic acid salts
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/06—Thio-acids; Thiocyanates; Derivatives thereof
    • C10M2219/062—Thio-acids; Thiocyanates; Derivatives thereof having carbon-to-sulfur double bonds
    • C10M2219/066—Thiocarbamic type compounds
    • C10M2219/068—Thiocarbamate metal salts
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
    • C10M2219/087—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
    • C10M2219/088—Neutral salts
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
    • C10M2219/087—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
    • C10M2219/089—Overbased salts
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04—Phosphate esters
    • C10M2223/045—Metal containing thio derivatives
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2227/00—Organic 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
    • C10M2227/06—Organic compounds derived from inorganic acids or metal salts
    • C10M2227/061—Esters derived from boron
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2227/00—Organic 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
    • C10M2227/06—Organic compounds derived from inorganic acids or metal salts
    • C10M2227/061—Esters derived from boron
    • C10M2227/062—Cyclic esters
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00—Metal present as such or in compounds
    • C10N2010/04—Groups 2 or 12
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00—Metal present as such or in compounds
    • C10N2010/12—Groups 6 or 16
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/40—Low content or no content compositions
    • C10N2030/42—Phosphor free or low phosphor content compositions
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/40—Low content or no content compositions
    • C10N2030/43—Sulfur free or low sulfur content compositions
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/40—Low content or no content compositions
    • C10N2030/45—Ash-less or low ash content
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/52—Base number [TBN]
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00—Specified use or application for which the lubricating composition is intended
    • C10N2040/25—Internal-combustion engines
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00—Specified use or application for which the lubricating composition is intended
    • C10N2040/25—Internal-combustion engines
    • C10N2040/251—Alcohol fueled engines
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00—Specified use or application for which the lubricating composition is intended
    • C10N2040/25—Internal-combustion engines
    • C10N2040/252—Diesel engines
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00—Specified use or application for which the lubricating composition is intended
    • C10N2040/25—Internal-combustion engines
    • C10N2040/255—Gasoline engines

Definitions

  • the present invention relates to a lubricating oil composition containing a dispersant package, a detergent package and antioxidant package.
  • the composition has improved engine cleanliness, improved detergency, decreased sludge formation and decreased wear.
  • lubricating oils It is well known for lubricating oils to contain a number of additives used to protect the engine from wear, the accumulation of sludge and filter plugging.
  • Common additives for engine lubricating oils are zinc dialkyldithiophosphate (ZDDP) as an antiwear additive, and overbased calcium sulphonate detergents. It is believed that ZDDP antiwear additives protect the engine by forming a protective film on metal surfaces.
  • Typical treatment quantities of ZDDP range from 1 to 2 weight percent based on the total weight of the lubricant. Detergents such as overbased calcium sulphonate help keep the engine parts clean of soot and other deposits, and offer an alkalinity reserve.
  • Typical treatment quantities of detergents range from 0.05 to 10 weight percent based on the total weight of the lubricant.
  • phosphates and sulphonates derived from engine lubricants have been shown to contribute in part to particulate emissions. Further, sulphur and phosphorus tend to poison the NO x catalysts used in catalytic converters, resulting in a reduction in performance of said catalysts. Any reduction in the performance of catalytic converters tends to result in increased amounts of pollutants such as nitric oxide and/or sulphur oxides. However, reducing the amount of ZDDP will increase the amount of wear in an engine. Also reducing the amount of detergent will decrease engine cleanliness and result in increased soot deposits.
  • US-A-6,200,936 discloses compounds containing phenolic units and salicylic units in a lubricating composition.
  • the compounds may be salted with calcium.
  • the examples of lubricating compositions contain phenolic units with a dodecyl alkyl group.
  • the compounds of the invention may be used as a detergent in gasoline or diesel fuel. They also stabilise gasoline or diesel compositions against thermal decomposition.
  • U.S.-A-6,310,009 (Kocsis et al. ) relates to the use of saligenin derivatives in lubricating compositions.
  • the formulations contain borated or non-borated magnesium saligenin derivatives. These compositions exhibit improved seal compatibility and reduced copper and lead corrosion.
  • composition of the present invention provides engine cleanliness, detergency and antioxidant performance to an oil of lubricating viscosity often used in engine oil.
  • the present invention provides a composition comprising:
  • the invention further provides a propcess for the preparation of the above composition comprising mixing:
  • composition of the invention is capable of imparting at least one or more of improved engine cleanliness, improved detergency, decreased sludge formation, decreased wear, decreased bore polishing and decreased oil consumption.
  • the present invention provides a composition as described above. Often the composition has a total sulphur content in one aspect below 0.5 wt %, in another aspect below 0.3 wt %, in yet another aspect 0.2 wt % or less and in yet another aspect 0.1 wt % or less. Often the major source of sulphur in the composition of the invention is derived from diluent oil.
  • the composition has a total phosphorus content of less than or equal to 800 ppm, in another aspect equal to or less than 700 ppm, in yet another aspect equal to or less than 600 ppm, in yet another aspect equal to or less than 550 ppm and in yet another aspect equal to or less than 500 ppm of the composition.
  • the phosphorus is present from 200 ppm or 300 ppm to 475 ppm or 580 ppm or even 780 ppm.
  • the composition has a total ash content as determined by ASTM D-874 of below 1.5 wt %, in one aspect equal to or less than 1.1 wt %, in another aspect equal to or less than 1.0 wt %, in yet another aspect equal to or less than 0.8 wt % and in yet another aspect equal to or less than 0.5 wt % of the composition.
  • the total ash content is present from 0.1 wt % or 0.2 wt % to 0.6 wt % or 0.7 wt%.
  • the detergent package contains a metal salixarate and optionally at least one detergent other than the metal salixarate.
  • the other detergent compounds are well known in the art and are often selected from the group consisting of a sulphonate, a phenate, a sulphurised phenate, a carboxylate, a phosphate, a saligenin, and an alkylsalicylate.
  • Saligenin chemistry is disclosed in more detail in US-A-6,310,009 .
  • Phenate, alkylsalicylate and phosphate chemistry is disclosed in " Chemistry and Technology of Lubricants," Edited by R.M. Mortier and S.T. Orszulik, 2nd Edition, Chapter 3, section 3.2.2, page 82 to 85, Copyright 1997 .
  • Sulphonate chemistry is disclosed in " Chemistry and Technology of Lubricants,” Edited by R.M. Mortier and S.T. Orszulik, 2nd Edition, Chapter 3, section 3.2.1, page 77 to 82,
  • the detergent compounds will be in the form of a metal salt or metal salts.
  • the metal is selected from an alkali metal or alkaline earth metal such as magnesium, calcium, potassium or sodium or mixtures thereof.
  • a metal detergent include a magnesium saligenin, a calcium saligenin, a calcium alkylsalicylate, a magnesium alkylsalicylate, a calcium sulphonate, a magnesium sulphonate or mixtures thereof.
  • the other detergent compound is a magnesium saligenin.
  • the detergent package often contains the metal of the metal salt present at 50 ppm to 1200 ppm, in one aspect 75 ppm to 1000 ppm, in another aspect 120 ppm to 800 ppm and in yet another aspect 150 ppm to 700 ppm, for example, about 225 ppm, about 275 ppm, about 325 ppm, about 400 ppm, or about 550 ppm or less.
  • the detergent package is often present on an oil free basis at 0.01 to 20, in one aspect 0.05 to 15, in another aspect 0.1 to 12, in another aspect 0.15 to 8 and in yet another aspect 0.25 to 4 weight percent of the composition.
  • the detergent contains the metal salixarate present at 10 wt % or more of the detergent package, in another aspect 20 wt % or more of the detergent package and in another aspect 30 wt % or more of the detergent package.
  • the metal salixarate is present at 0.25 to 4 weight percent of the composition.
  • the substrate of the metal salixarate of the invention is often represented by a substantially linear compound comprising at least one unit of the formulae (I) or (II): or each end of the compound having a terminal group of formulae (III) or (IV): such groups being linked by divalent bridging groups, which may be the same or different for each linkage; wherein in formulas (I)-(IV) f in one aspect is 1, 2 or 3, in another aspect 1 or 2; U is -OH, -NH 2 -NHR 1 , -N(R 1 ) 2 or mixtures thereof, R 1 is a hydrocarbyl group containing 1 to 5 carbon atoms; R 2 is hydroxyl or a hydrocarbyl group and j is 0, 1, or 2; R 3 is hydrogen or a hydrocarbyl group; R 4 is a hydrocarbyl group or a substituted hydrocarbyl group; g is 1, 2 or 3, provided at least one R 4 group contains 8 or more carbon atoms; and wherein the molecules on average contain
  • the U group in formulae (i) and (iii) may be located in one or more positions ortho, meta, or para to the -COOR 3 group. In one embodiment of the invention, the U group is located ortho to the -COOR 3 group.
  • formulae (i) and (iii) are derived from 2-hydroxybenzoic acid (often called salicylic acid), 3-hydroxybenzoic acid, 4-hydroxybenzoic acid or mixtures thereof.
  • U is a -NH 2 group
  • formulae (i) and (iii) are derived from 2-aminobenzoic acid (often called anthranilic acid), 3-aminobenzoic acid, 4-aminobenzoic acid or mixtures thereof.
  • the divalent bridging group which may be the same or different in each occurrence, includes -CH 2 - (methylene bridge) and -CH 2 OCH 2 - (ether bridge), either of which may be derived from an aldehyde such as formaldehyde or a formaldehyde equivalent (e.g., paraform, formalin), ethanal or propanal.
  • aldehyde such as formaldehyde or a formaldehyde equivalent (e.g., paraform, formalin), ethanal or propanal.
  • the metal of the metal salixarate is often mono-valent, di-valent or mixtures thereof.
  • the metal is selected from an alkali metal or alkaline earth metal such as magnesium, calcium, potassium or sodium or mixtures thereof.
  • each R 5 may be the same or different, and are hydrogen or an alkyl group, provided at least one R 5 is alkyl.
  • R 5 is a polyisobutene group (especially of molecular weight 200 to 1,000, or 550).
  • Significant amounts of di-or trinuclear species may also be present containing one salicylic end group of formula (III).
  • the salixarate detergent may be used alone or with other detergents.
  • Salixarate derivatives and methods of their preparation are described in greater detail in U.S. patent number 6,200,936 and PCT Publications WO 01/56968 and WO 03/18728 .
  • the dispersants of the invention are often derived from N-substituted long chain alkenyl succinimides.
  • the invention requires at least 2 dispersants, one with a high Total Base Number and one with a high Total Acid Number.
  • dispersants with a high TAN number have a carbonyl to nitrogen ratio of 1 or higher, in one aspect 1.2 or higher, in another aspect 1.4 or higher and in yet another aspect 1.45 or higher, for example 1.5.
  • Generally dispersants with a high TBN number have a carbonyl to nitrogen ratio of less than 1, in one aspect 0.94 or lower, in another aspect 0.88 or lower and in another aspect 0.8 or lower, for instance 0.77.
  • the carbonyl to nitrogen ratio is to be calculated on a molar basis, that is, the ratio of moles of carbonyl functionality (e.g., -C(O)O- ) to the moles of nitrogen functionality (e.g., amine nitrogens).
  • the dispersant package is present on an oil free basis at 0.01 to 30, in one aspect 0.5 to 25, in another aspect 1.5 to 20 and in yet another aspect 3 to 15 weight percent of the composition.
  • the dispersant with a high Total Base Number is present at lower concentration than the dispersant with a high Total Acid Number.
  • the amount of dispersant with a high Total Acid Number and a high Total Base Number is equal.
  • the dispersant with a high Total Acid Number is often present at lower concentration than the dispersant with a high Total Base Number.
  • the dispersant present in the greater quantity is present at greater than 50% of the amount of dispersant present in the package, in one aspect greater than 55% of the amount of dispersant present in the package, in yet another aspect greater than 60% of the amount of dispersant present in the package.
  • the dispersant present in the greater quantity may be present from 61% to 95% of the dispersant, in one aspect 62% to 90% of the dispersant and in yet another aspect 63% to 85% of the dispersant present in the package.
  • the ratio of high TAN dispersant to high TBN dispersant is 1:1 to 15:1, in another aspect 2:1 to 10:1 and in another aspect 3:1 to 6:1.
  • the mixture of dispersants has a TAN which is at least 15% or at least 20% of the TBN of the mixture of dispersants, for example, 15 to 30% of the TBN. In certain embodiments the TBN/TAN ratio for the mixture of dispersants is 3:1 to 7:1.
  • the N-substituted long chain alkenyl succinimides have a variety of chemical structures and include a mono-succinimide and/or a di-succinimide.
  • the long chain alkenyl group will have number average molecular weight of 350 to 10,000, in one aspect 400 to 7000, in another aspect 500 to 5000 and in yet another aspect 500 to 4000.
  • the long chain alkenyl group is a polyisobutylene group, which has a number average molecular weight from 800 to 1600 and in another embodiment from 1600 to 3000.
  • the succinimide is often prepared by the condensation of a hydrocarbyl-substituted acylating agent (e.g., hydrocarbyl-substituted succinic anhydride) with a polyamine or an amino alcohol, often a polyalkylene polyamine or poly(ethyleneamine) such as triethylene tetramine, tetraethylene pentamine, pentaethylene hexamine or, in one embodiment, polyamine still bottoms.
  • a hydrocarbyl-substituted acylating agent e.g., hydrocarbyl-substituted succinic anhydride
  • a polyamine or an amino alcohol often a polyalkylene polyamine or poly(ethyleneamine) such as triethylene tetramine, tetraethylene pentamine, pentaethylene hexamine or, in one embodiment, polyamine still bottoms.
  • N-substituted long chain alkenyl succinimides dispersant additives and their preparation are disclosed, for instance, in US-A-3,361,673 , 3,401,118 and 4,234,435 .
  • dispersants may also be present.
  • suitable dispersants include Mannich bases, which are the reaction products of alkyl phenols in which the alkyl group typically contains at least 30 carbon atoms with aldehydes (especially formaldehyde) and amines (especially polyalkylene polyamines) and are described in more detail in U.S.-A-3,634,515 .
  • ashless dispersant is high molecular weight esters. These materials are similar to the above-described succinimides except that they may be seen as having been prepared by reaction of a hydrocarbyl acylating agent and a polyhydric aliphatic alcohol such as glycerol, pentaerythritol, or sorbitol. Such materials are described in more detail in U.S.-A-3,381,022 .
  • dispersants include polymeric dispersant additives, which are generally hydrocarbon-based polymers which contain polar functionality to impart dispersancy characteristics to the polymer.
  • Dispersants may also be post-treated by reaction with any of a variety of agents. Among these are urea, thiourea, dimercaptothiadiazoles, carbon disulfide, aldehydes, ketones, carboxylic acids, hydrocarbon-substituted succinic anhydrides, nitriles, epoxides, boron compounds, and phosphorus compounds. References detailing such treatment are listed in U.S.-A-4,654,403 . (The carbonyl to nitrogen ratio herein is calculated prior to any such post-treatment.)
  • N-substituted long chain alkenyl succinimide dispersants There are two commonly employed processes for making N-substituted long chain alkenyl succinimide dispersants. These differ in the method by which a polyalkylene (typically polyisobutylene, but also copolymers including ethylene copolymer) substituent is prepared and by which it is affixed to a mono- or diacid or anhydride moiety, especially a succinic anhydride moiety or its reactive equivalent.
  • a polyalkylene typically polyisobutylene, but also copolymers including ethylene copolymer
  • isobutylene is polymerised in the presence of AlCl 3 to produce a mixture of polymers comprising predominantly tri-substituted olefin and tetra-substituted olefin end groups, with only a very small amount (for instance, less than 20 percent) of chains containing a terminal vinylidene group.
  • isobutylene is polymerised in the presence of BF 3 catalyst to produce a mixture of polymers comprising predominantly (for instance, at least 70 percent) terminal vinylidene groups, with smaller amounts of tetra-substituted end groups and other structures.
  • a dispersant with a carbonyl to nitrogen ratio of 1 or higher; or a dispersant with a carbonyl to nitrogen ratio of less than 1 may be prepared using either process.
  • Amines which may be used in preparing dispersants include those with at least one reactive N-H group. Suitable examples of an amine are selected from the group consisting of an amine compound containing only a single reactive amino group per molecule; (ii) a polyamine; (iii) an aminoalcohol; (iv) a cyclic amine; and (v) mixtures of (i) to (iv).
  • the polyamine is an alkylenepolyamine often selected from the group consisting of an ethylenepolyamine, a propylenepolyamine, a butylenepolyamine and mixtures thereof.
  • a propylenepolyamine include propylenediamine, dipropylenetriamine or mixtures thereof.
  • An especially useful class of amine is derived from an ethylenepolyamines, selected from the group consisting of ethylenediamine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine, pentaethylenehexamine, polyamine still bottoms and mixtures thereof.
  • the polyamine includes a ⁇ , ⁇ -diaminoalkane or mixtures thereof.
  • Suitable examples of the ⁇ , ⁇ -diaminoalkane include a diaminopropane, a diaminobutane or mixtures thereof.
  • a diaminoalkanes include those selected from the group consisting of N-(2-aminoethyl)-1,3-propane diamine, 3,3'-diamine-N-methyldipropylamine, tris(2-aminoethyl)amine, N,N-bis(3-aminopropyl)-1,3-propane diamine, N,N'-1,2-ethanediylbis-(1,3-propane diamine) and mixtures thereof.
  • another polyamine includes di-(trimethylene)triamine, piperazine, diaminocyclohexanes or mixtures thereof.
  • Aminoalcohols suitable for the invention contain 1 to 6 and in one aspect 1 to 3 hydroxy groups; and 1 to 8 and in one aspect 1 to 2 amine groups.
  • the amine is often selected from the group consisting of ethanolamine, isopropanolamine, diethanolamine, triethanolamine, diethylethanolamine, dimethylethanolamine, dibutylethanolamine, 3-amino-1,2-propanediol; serinol; 2-amino-2-methyl-1,3-propanediol; tris(hydroxymethyl)-aminomethane; 1-amino-1-deoxy-D-sorbitol; diethanol amine; diisopropanolamine; N-methyl-N,N-diethanol amine; triethanolamine; N,N,N',N'-tetrakis(2-hydroxypropyl)ethylenediamine, 2-amino-2-methyl-1-propanol, 2-dimethylamino-methyl-1
  • the hindered phenol suitable for the invention is often represented by the formula: wherein R 6 and R 7 are independently branched or linear alkyl groups containing in one aspect 1 to 24, in another aspect 4 to 18, and in yet another aspect 4 to 12 carbon atoms; and E is hydrogen, a hydrocarbyl group, a bridging group linking to a second aromatic group, an ester-containing group, or mixtures thereof.
  • R 6 and R 7 may be either straight or branched chain and suitable examples include secondary butyl and tertiary butyl.
  • the hindered phenol of formula (VI) suitable for the invention are esters or acids represented by the formula: wherein R 6 and R 7 are as defined above and R 8 is hydrogen, a hydrocarbyl group or mixtures thereof.
  • R 8 is a hydrocarbyl group
  • R 8 is often selected from the group consisting of butyl, sec-butyl, isobutyl, tert-butyl, pentyl, n-hexyl, sec-hexyl, n-octyl, 2-ethylhexyl, nonyl, decyl, undecyl, dodecyl and mixtures thereof.
  • the hindered phenol of formula (VI) suitable for the invention contains a bridging group.
  • suitable bridging groups include an alkylene bridge or an ether bridge, often containing 1 to 8, in one aspect 1 to 6, in another aspect 1 to 4 and in yet another aspect 1 to 2 carbon atoms.
  • Examples of a suitable bridge group include -CH 2 -, -CH 2 CH 2 -, -CH 2 OCH 2 - and -CH 2 CH 2 OCH 2 CH 2 -.
  • the hindered phenol with a bridging group is often represented by the formula: wherein R 6 and R 7 are defined above and Y is a bridging group.
  • Examples of a methylene-bridged hindered phenol include 4,4'-methylene-bis-(6-tert-butyl-o-cresol), 4,4'-methylene-bis-(2-tert-amyl-o-cresol) and 4,4 -methylene-bis-(2,6-di-tertbutylphenol).
  • the hindered phenol of the invention also includes compounds represented by the formula: wherein R 6 and R 7 , E and Y are defined above.
  • suitable methylene-bridged hindered phenol of formula (VII) include 2,2'-methylene-bis-(4-methyl-6-tert-butylphenol), and 2,2'-methylene-bis-(4-ethyl-6-tertbutylphenol), 2,2 -methylene-bis-(4-propyl-6-tert-butylphenol).
  • the antioxidant package is often present on an oil free basis at 0.01 to 20, in one aspect 0.1 to 15, in another aspect 0.5 to 10 and in yet another aspect 1 to 5 weight percent of the composition.
  • at least 50 wt % of the antioxidant package is a hindered phenol.
  • the hindered phenol is present at 0.2 to 3 weight percent of the composition; alternatively 0.01 to 15 or 0.05 to 10 or 0.1 to 5 or 0.5 to 4 weight percent..
  • the lubricating oil composition of the present invention may be added to an oil of lubricating viscosity.
  • the oil includes natural and synthetic oils, oil derived from hydrocracking, hydrogenation, hydrofinishing, unrefined, refined and re-refined oils, or mixtures thereof.
  • Unrefined oils are those obtained directly from a natural or synthetic source generally without (or with little) further purification treatment.
  • Refined oils are similar to the unrefined oils except they have been further treated in one or more purification steps to improve one or more properties.
  • Purification techniques include solvent extraction, secondary distillation, acid or base extraction, filtration, percolation and the like.
  • Re-refined oils are also known as reclaimed or reprocessed oils, and are obtained by processes similar to those used to obtain refined oils and often are additionally processed by techniques directed to removal of spent additives and oil breakdown products.
  • Natural oils useful in making the inventive lubricants include animal oils, vegetable oils (e.g., castor oil, lard oil), mineral lubricating oils such as liquid petroleum oils and solvent-treated or acid-treated mineral lubricating oils of the paraffinic, naphthenic or mixed paraffinic-naphthenic types and oils derived from coal or shale or mixtures thereof.
  • animal oils e.g., castor oil, lard oil
  • mineral lubricating oils such as liquid petroleum oils and solvent-treated or acid-treated mineral lubricating oils of the paraffinic, naphthenic or mixed paraffinic-naphthenic types and oils derived from coal or shale or mixtures thereof.
  • Synthetic lubricating oils are useful and include hydrocarbon oils such as polymerised and interpolymerised olefins (e.g., polybutylenes, polypropylenes, propyleneisobutylene copolymers); poly(1-hexenes), poly(1-octenes), poly(1-decenes), and mixtures thereof; alkyl-benzenes (e.g.
  • dodecylbenzenes tetradecylbenzenes, dinonylbenzenes, di-(2-ethylhexyl)-benzenes
  • polyphenyls e.g., biphenyls, terphenyls, alkylated polyphenyls
  • Synthetic lubricating oils include but are not limited to polyol esters, liquid esters of phosphorus-containing acids (e.g., tricresyl phosphate, trioctyl phosphate, and the diethyl ester of decane phosphonic acid), and polymeric tetrahydrofurans.
  • Synthetic oils may be produced by Fischer-Tropsch reactions and typically may be hydroisomerised Fischer-Tropsch hydrocarbons or waxes.
  • Oils of lubricating viscosity may also be defined as specified in the American Petroleum Institute (API) Base Oil Interchangeability Guidelines.
  • the five base oil groups are as follows: Group I (sulphur content >0.03 wt %, and/or ⁇ 90 wt % saturates, viscosity index 80-120); Group II (sulphur content ⁇ 0.03 wt %, and ⁇ 90 wt % saturates, viscosity index 80-120); Group III (sulphur content ⁇ 0.03 wt %, and ⁇ 90 wt % saturates, viscosity index ⁇ 120); Group IV (all polyalphaolefins (PAO's)); and Group V (all others not included in Groups I, II, III, or IV).
  • PAO's polyalphaolefins
  • the oil of lubricating viscosity is selected from the group consisting of an API Group I, II, III, IV, V oil and mixtures thereof; in one aspect an API Group II, III, IV or V oil and mixtures thereof; and in yet another aspect an API Group III, IV or V oil and mixtures thereof. If the oil of lubricating viscosity is an API Group II, III, IV or V oil there may be up to a maximum of 20 wt %, in one aspect up to a maximum of 10 wt %, in anther aspect up to a maximum of 5 wt % and in yet another aspect up to a maximum of 1.5 wt % of the lubricating oil an API Group I oil.
  • Suitable API Group III oils include NexbaseTM 3050, NexbaseTM 3043, NexbaseTM 3060, PAO-6, PriolubeTM 1976, YubaseTM 4, YubaseTM 6, and ShellTM XHVI 5.2.
  • the oil of lubricating viscosity is often present at up to 99.97, in one aspect up to 99.69, in another aspect up to 97.75 and in yet another aspect up to 95.5 weight percent of the composition.
  • the composition is often classed as a SAE XW-Y lubricating oil, wherein X is 0 or 5; and Y is 20, 30, 40 or 50.
  • the present invention is in the form of a concentrate (which may be combined with additional oil to form, in whole or in part, a finished lubricant), the ratio of each of the above-mentioned dispersant, as well as other components, to diluent oil is often 80:20 to 10:90 by weight.
  • composition of the invention optionally further includes other performance additives.
  • the other performance additives selected from the group consisting of antioxidants other than component (c), corrosion inhibitors, antiwear agents, friction modifiers, viscosity modifiers, antiscuffing agents, foam inhibitors, demulsifiers, pour point depressants, seal swelling agents and mixtures thereof.
  • the total combined amount of the other performance additives present on an oil free basis is often from 0 to 25, in one aspect 0.01 to 20, in another aspect 0.05 to 15 and in yet another aspect 0.1 to 10 weight percent of the composition. Although one or more of the other performance additives may be present, it is common for the other performance additives to be present in different amounts relative to each other.
  • the friction modifier may be a monoester of a polyol and an aliphatic carboxylic acid, often an acid containing 12 to 24 carbon atoms.
  • the monoester of a polyol and an aliphatic carboxylic acid is in the form of a mixture with a sunflower oil or the like, which may be present in the friction modifier mixture from 5 to 95, in one aspect 10 to 90, in another aspect 20 to 85 and in yet another aspect 20 to 80 weight percent of said mixture.
  • Polyols include diols, triols, and alcohols with higher numbers of alcoholic OH groups.
  • Polyhydric alcohols include ethylene glycols, including di-, tri- and tetraethylene glycols; propylene glycols, including di-, tri- and tetrapropylene glycols; glycerol; butane diol; hexane diol; sorbitol; arabitol; mannitol; sucrose; fructose; glucose; cyclohexane diol; erythritol; and pentaerythritols, including di- and tripentaerythritol.
  • the polyol is diethylene glycol, triethylene glycol, glycerol, sorbitol, pentaerythritol or dipentaerythritol.
  • the aliphatic carboxylic acids which form the esters are those acids containing 12 to 24 carbon atoms. Acids containing straight chain hydrocarbyl groups containing 12 to 24 carbon atoms are often used, for instance, 14 to 20 or 16 to 18 carbon atoms. Such acids may be used in combination with acids with more or fewer carbon atoms as well. Generally the acid is a monocarboxylic acid. Examples of carboxylic acids include dodecanoic acid, stearic acid, lauric acid, behenic acid, and oleic acid.
  • the esters used in the present invention are in particular the monoesters of such polyols and such carboxylic acids. Often the ester is glycerol monooleate. It is to be understood that glycerol monooleate, as is the case with other such materials, in its commercially available grade, is a mixture which includes such materials as glycerol, oleic acid, other long chain acids, glycerol dioleate, and glycerol trioleate. The commercial material is believed to include 60 ⁇ 5 percent by weight of the chemical species "glycerol monooleate," along with 35 ⁇ 5 percent glycerol dioleate, and less than 5 percent trioleate and oleic acid. The amounts of the monoesters, described below, are calculated based on the actual, corrected, amount of polyol monoester present in any such mixture.
  • friction modifiers that are suitable for the invention include fatty amines, fatty phosphites, fatty acid amides, fatty epoxides, alkoxylated fatty amines, metal salts of fatty acids, sulphurised olefins, fatty imidazolines, condensation products of carboxylic acids and polyalkylene-polyamines, amine salts of alkylphosphoric acids.
  • the invention includes an antioxidant other than a hindered phenol, such as, a diphenylamine antioxidant, a molybdenum dithiocarbamate, a sulphurised olefin, or mixtures thereof.
  • Diphenylamine antioxidant additives often contain in one aspect 6 or fewer, in another aspect 4 or fewer and in yet another aspect 3 or fewer hydrocarbyl groups such as 1 or 2. Each hydrocarbyl group often contains in one aspect 1 to 24, in another aspect 2 to 18 and in yet another aspect 4 to 12 carbon atoms.
  • the composition contains a diphenylamine antioxidant.
  • diphenylamine antioxidants examples include octyl diphenylamine, nonyl diphenylamine, bis-octyl diphenylamine, and bis-nonyl diphenylamine.
  • the invention contains a viscosity modifier.
  • Viscosity modifiers are known and include polymeric materials including hydrogenated styrene-butadiene rubbers, an olefin copolymer, hydrogenated styrene-isoprene polymers, hydrogenated radical isoprene polymers, polymethacrylate acid esters, polyacrylate acid esters, polyalkyl styrenes, alkenyl aryl conjugated diene copolymers, polyalkylmethacrylates, esters of maleic anhydride-styrene copolymers or mixtures thereof.
  • polymethacrylate viscosity modifiers include copolymers of (a) a methacrylic acid ester containing 9 to 30 carbons in the ester group, (b) a methacrylic acid ester containing 7 to 12 carbons in the ester group wherein the ester group contains a 2-(C 1-4 alkyl)-substituent and optionally (c) at least one monomer selected from the group consisting of a methacrylic acid ester containing from 2 to 8 carbon atoms in the ester group and which are different from methacrylic acid esters used in (a) and (b) above.
  • a more detailed description of polymethacrylate viscosity modifiers is disclosed in US-A-6,124,249 .
  • viscosity modifiers derived from an olefin copolymer backbone contain in one aspect 2 to 4, in another aspect 2 to 3 and in yet another aspect 2 different olefin monomers.
  • the olefin monomers often contain in one aspect 2 to 20, in another aspect 2 to 10, in yet another aspect 2 to 6 and in yet another aspect 2 to 4 carbon atoms.
  • R 8 is a hydrocarbyl group, in one aspect an alkyl radical containing 1 to 18, in one aspect 1 to 10, in another aspect 1 to 6 and in yet another aspect 1 to 3 carbon atoms.
  • the hydrocarbyl group includes an alkyl radical that has a straight chain, a branched chain or mixtures thereof.
  • Examples of a suitable comonomer include propylene, 1-butene, 1-hexene, 1-octene, 4-methylpentene-1, 1-decene, 1-dodecene, 1-tridecene, 1-tetradecene, 1-pentadecene, 1-hexadecene, 1-heptadecene, 1-octadecene, 1-nonadecene or mixtures thereof.
  • Examples of the olefin copolymers include ethylene-propylene copolymers, ethylenebutene-1 copolymers and mixtures thereof.
  • the viscosity modifier comprises a mixture of 2 copolymers derived from (A) a copolymer comprising 45 to 85 % by weight of units derived from ethylene, having a M w of 50,000 to 300,000, M w / M n less than 3, and a melting point of 0°C to 60°C; and (B) a block copolymer comprising a vinyl aromatic comonomer moiety and a second comonomer moiety.
  • the copolymer (A) is often prepared by copolymerising ethylene and other monomers, usually propylene.
  • the monomers which may be used to prepare the (B) copolymers of the present inventions are 1,3-butadiene, 1,2-pentadiene, 1,3-pentadiene, isoprene, 1,5-hexadiene, and 2-chloro-1,3 butadiene, and aromatic olefins such as styrene, ⁇ -methyl styrene, ortho-methyl styrene, meta-methyl styrene, para-methyl styrene, and para-t-butyl styrene, and mixtures thereof.
  • aromatic olefins such as styrene, ⁇ -methyl styrene, ortho-methyl styrene, meta-methyl styrene, para-methyl styrene, and para-t-butyl styrene, and mixtures thereof.
  • Other comonomers may be included in the mixture and in the polymer, which do
  • Suitable styrene/isoprene hydrogenated copolymers are available commercially from Infineum under the trade names InfineumTM SV140 (formerly ShellvisTM 40) (M w ca. 200,000), InfineumTM SF150 (M w ca. 150,000) and InfineumTM SV160 (M w ca. 150,000), as well as from Septon Company of America (Kuraray Group) under the trade names SeptonTM 1020 (M w ca. 150,000) and SeptonTM 1001 (M w ca. 200,000).
  • Suitable styrene/1,3-butadiene hydrogenated random block copolymers are available from BASF under the trade name GlissoviscalTM (M w ca. 160,000-220,000).
  • the viscosity modifier copolymers are further grafted with an unsaturated dicarboxylic acid anhydride or derivatives thereof and an amine to form a dispersant viscosity modifier (often referred to as DVM), thus named, because they also exhibit dispersant properties.
  • DVM dispersant viscosity modifier
  • the invention optionally includes an antiwear agent such as a metal hydrocarbyl dithiophosphate often represented by the formula: wherein R 9 and R 10 are independently hydrogen, hydrocarbyl groups or mixtures thereof, provided that at least one of R 9 and R 10 is a hydrocarbyl group, often containing in one aspect 1 to 30, in another aspect 2 to 20 and in yet another aspect 2 to 15 carbon atoms.
  • an antiwear agent such as a metal hydrocarbyl dithiophosphate often represented by the formula: wherein R 9 and R 10 are independently hydrogen, hydrocarbyl groups or mixtures thereof, provided that at least one of R 9 and R 10 is a hydrocarbyl group, often containing in one aspect 1 to 30, in another aspect 2 to 20 and in yet another aspect 2 to 15 carbon atoms.
  • M' is a metal, and n is an integer equal to the available valence of M'.
  • M' is mono- or di- or tri- valent, in one aspect M' is divalent and in another aspect a divalent transition metal.
  • M' is zinc.
  • M' is calcium.
  • M' is barium.
  • Examples of a metal hydrocarbyl dithiophosphate include zinc dihydrocarbyl dithiophosphates (often referred to as ZDDP, ZDP or ZDTP).
  • the invention further contains a borate ester antiwear agent.
  • the borate ester may be prepared by the reaction of a boron compound and at least one compound selected from epoxy compounds, halohydrin compounds, epihalohydrin compounds, alcohols and mixtures thereof. Often the alcohols include monohydric alcohols, dihydric alcohols, trihydric alcohols or higher alcohols.
  • Boron compounds suitable for preparing the borate ester include the various forms selected from the group consisting of boric acid (including metaboric acid, HBO 2 , orthoboric acid, H 3 BO 3 , and tetraboric acid, H 2 B 4 O 7 ), boric oxide, boron trioxide and alkyl borates.
  • the borate ester may also be prepared from boron halides.
  • the borate ester formed by the reaction of a boron compound and an epoxy compound may be represented by at least one compound derived from the formulae: wherein R 11 , R 12 and R 13 may be hydrogen or hydrocarbyl groups provided at least one, in one aspect at least two of R 11 , R 12 and R 13 are hydrocarbyl groups.
  • R 11 is a hydrocarbyl group; and R 12 and R 13 are hydrogen.
  • R 11 and R 12 are hydrocarbyl groups and R 13 is hydrogen.
  • R 11 , R 12 and R 13 are all hydrocarbyl groups.
  • the hydrocarbyl groups may be alkyl, aryl or cycloalkyl when any 2 adjacent R groups are connected in a ring.
  • the number of carbon atoms in the hydrocarbyl groups may be 1 to 60, or 1 to 40 or even 1 to 30 carbon atoms, provided the total number of carbon atoms in R 11 , R 12 and R 13 is 9 or more, in one aspect 10 or more, in another aspect 12 or more and in yet another aspect 14 or more.
  • R 14 to R 20 inclusive may be hydrogen or hydrocarbyl groups, provided at least one of R 14 to R 17 and/or R 18 to R 20 is a hydrocarbyl group.
  • R 21 to R 26 inclusive are independently hydrogen or a hydrocarbyl group, although it is common for at least one of R 21 to R 26 to be a hydrocarbyl group; and
  • R 27 may be hydrogen or a hydrocarbyl group, although it is common for R 27 to be hydrogen.
  • the hydrocarbyl group definition for R 14 to R 27 inclusive is the same as the definition given for R 11 , R 12 and R 13 .
  • R 11 to R 27 inclusive examples include isopropyl, n-butyl, isobutyl, amyl, 2-pentenyl, 4-methyl-2-pentyl, 2-ethyl-1-hexyl, 2-ethylhexyl, heptyl, isooctyl, nonyl, decyl, undecyl, dodecenyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl and eicosyl groups.
  • Suitable examples of the optional borate ester include tripropyl borate, tributyl borate, tripentyl borate, trihexyl borate, triheptyl borate, trioctyl borate, trinonyl borate and tridecyl borate. Borate ester compounds are discussed in more detail in EP-A-976 814 .
  • composition of the invention optionally contains antiwear agent additives other than a metal hydrocarbyl dithiophosphate including phosphoric acid esters or salts thereof; phosphites; and phosphorus-containing carboxylic esters, ethers, and amides or mixtures thereof.
  • antiwear agent additives other than a metal hydrocarbyl dithiophosphate including phosphoric acid esters or salts thereof; phosphites; and phosphorus-containing carboxylic esters, ethers, and amides or mixtures thereof.
  • antiwear agent additives other than a metal hydrocarbyl dithiophosphate including phosphoric acid esters or salts thereof; phosphites; and phosphorus-containing carboxylic esters, ethers, and amides or mixtures thereof.
  • phosphoric acid esters contain a hydrocarbyl ester group with 4 to 40, in one aspect 4 to 30 and in another aspect 6 to 24 carbon atoms.
  • the hydrocarbyl ester group is alkyl and in
  • optional performance additives include, for example, corrosion inhibitors octylamine octanoate, condensation products of dodecenyl succinic acid or anhydride and a fatty acid such as oleic acid with a polyamine; metal deactivators including derivatives of benzotriazoles, 1,2,4-triazoles, benzimidazoles, 2-alkyldithiobenzimidazoles or 2-alkyldithiobenzothiazoles; foam inhibitors including copolymers of ethyl acrylate and 2-ethylhexylacrylate and optionally vinyl acetate; demulsifiers including trialkyl phosphates, polyethylene glycols, polyethylene oxides, polypropylene oxides and (ethylene oxide-propylene oxide) polymers; pour point depressants including esters of maleic anhydride-styrene, polymethacrylates, polyacrylates or polyacrylamides; and seal swell agents including Exxon Necton-37TM
  • the invention further provides a process for the preparation of a composition as described above.
  • Components (a)-(d) are often mixed sequentially, separately for the composition of the invention, although two or more of the components may also be mixed simultaneously.
  • the mixing conditions are often 15°C to 130°C, in one aspect 20°C to 120°C and in another aspect 25°C to 110°C; and for a period of time in the range 30 seconds to 48 hours, in one aspect 2 minutes to 24 hours, in another aspect 5 minutes to 16 hours and in yet another aspect 10 minutes to 5 hours; and at pressures in the range 86 kPa to 266 kPa (650 mm Hg to 2000 mm Hg), in one aspect 91 kPa to 200 kPa (690 mm Hg to 1500 mm Hg), and in another aspect 95 kPa to 133 kPa (715 mm Hg to 1000 mm Hg).
  • the process optionally includes mixing other optional performance additives as described above.
  • the optional performance additives are often added sequentially, separately or as a concentrate.
  • composition of the present invention is useful as a lubricant in internal combustion engines, for example diesel fuelled engines, gasoline fuelled engines, natural gas fuelled engines or a mixed gasoline/alcohol fuelled engines.
  • composition of the invention provides a method for lubricating an internal combustion engine, comprising supplying thereto a lubricant comprising the composition as described herein.
  • the use of the composition of the invention is capable of imparting at least one or more of improved engine cleanliness, improved detergency, decreased sludge formation, decreased wear, decreased bore polishing and decreased oil consumption.
  • Reference Example 1 is a 5W-30 lubricating oil containing on an oil free basis about 6% of succinimide dispersants, with the high TAN dispersant present in higher quantity than the high TBN dispersant; on an oil free basis about 2.8 wt % hindered phenol antioxidant; and a detergent package containing an alkylsalicylate (AC60C® commercially available from Infineum) present on an oil free basis at about 1.1 wt %.
  • the lubricating oil has a phosphorus content of 480 ppm and a sulphated ash content of 0.49 wt %.
  • Example 1 is the same as Reference Example 1, except the detergent package containing alkylsalicylate is replaced by a calcium sulphonate detergent and a calcium salixarate detergent (each commercially available from The Lubrizol Corporation) together present on an oil free basis at about 1.1 wt %.
  • a calcium sulphonate detergent and a calcium salixarate detergent each commercially available from The Lubrizol Corporation
  • Reference Example 2 is the same as Example 1, except the high TAN dispersant is used alone.
  • Reference Example 3 is the same as Reference Example 1, except the detergent package containing alkylsalicylate is replaced by a calcium sulphonate and a calcium phenate.
  • Example 2 is the same as Reference Example 1, except the detergent package containing alkylsalicylate is replaced by calcium sulphonate, a calcium phenate and a calcium salixarate.
  • Blends are prepared of a 50:50 mixture by weight of an ethylene-propylene copolymer (Polymer A) and a styrene/isoprene hydrogenated copolymer (Polymer B), each of which are commercially available viscosity modifiers.
  • Polymer A is first dissolved in a 150N mineral oil containing 0.1% of a butylated hydroxytoluene (BHT) antioxidant. The antioxidant is added to the mineral oil at room temperature.
  • BHT butylated hydroxytoluene
  • the oil is continued to be heated to 130°C and is maintained at that temperature until all the Polymer A pellets are fully dissolved.
  • Polymer B which is also in a pellet form, is then added to the oil with strong agitation at 130°C until all of Polymer B is fully dissolved.
  • the blends are maintained at 130°C under strong agitation for an additional two hours to ensure that all the polymers are fully soluble.
  • Example 3 is a 5W-30 lubricating oil containing on an oil free basis about 6% of succinimide dispersants, with a high TAN dispersant present in higher quantity than the high TBN dispersant; on an oil free basis about 2.8% hindered phenol antioxidant; and a detergent package containing only a calcium salixarate on an oil free basis at 1.2 wt % and an olefin copolymer viscosity modifier present on an oil free basis at about 1 wt %.
  • the lubricating oil has a phosphorus content of 480 ppm and a sulphated ash content of 0.44 wt %.
  • Example 4 is the same as Example 3, except the viscosity modifier is the product of Preparative Example A.
  • Reference Example 4 is the same as Reference Example 3, except the composition contains an antioxidant package with a hindered phenol and a diphenylamine.
  • the detergent package is present at about 1.1 wt %.
  • the lubricating oil has a phosphorus content of 760 ppm and an ash content of 0.76 wt %.
  • Comparing Example 1 and Reference Example 1 indicates that a (a) dispersant package with a high TAN dispersant, a high TBN dispersant detergent package containing a salixarate; and a hindered phenol antioxidant package improves piston cleanliness compared with a detergent package free of salixarate. Likewise comparing Example 2 and Reference Example 3 again indicates the piston cleanliness properties of the composition of the invention.
  • Comparing Comparative Example 3 and Example 4 indicates that the composition of the invention has piston cleanliness properties even in the presence of viscosity modifiers.
  • composition of the invention has improved piston cleanliness, decreased bore polishing and decreased oil consumption compared with the reference example.
  • Other measurements shown in Table 3 are within acceptable limits.
  • composition of the invention improves engine cleanliness, improves detergency, decreases sludge formation, decrease wear, decreased bore polishing and decreased oil consumption.
  • hydrocarbyl substituent or “hydrocarbyl group,” as used herein are used in its ordinary sense, which is well-known to those skilled in the art. Specifically, it refers to a group primarily composed of carbon and hydrogen atoms and attached to the remainder of the molecule through a carbon atom and which does not exclude the presence of other atoms or groups in a proportion insufficient to detract from the molecule having a predominantly hydrocarbon character. In general, no more than two, in one aspect no more than one, non-hydrocarbon substituent will be present for every ten carbon atoms in the hydrocarbyl group; typically, there will be no non-hydrocarbon substituents in the hydrocarbyl group. A more detailed definition of the terms “hydrocarbyl substituent” or “hydrocarbyl group,” is provided in US-A-6,583,092 .
  • each chemical or composition referred to herein should be interpreted as being a commercial grade material which may contain the isomers, by-products, derivatives, and other such materials which are normally understood to be present in the commercial grade. However, the amount of each chemical component is presented exclusive of any solvent or diluent oil, which may be customarily present in the commercial material, unless otherwise indicated.

Landscapes

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

Claims (15)

  1. Composition, comprenant:
    (a) de 0,01 à 20 pour cent en poids, sur produit sans huile et par rapport au poids de la composition, d'un système de tensioactifs, comprenant:
    (i) de 0,25 à 4 pour cent en poids de la composition d'un salixarate métallique; et
    (ii) éventuellement un tensioactif autre que le composant (a)(i);
    (b) de 0,01 à 30 pour cent en poids, sur produit sans huile et par rapport au poids de la composition, d'un système de dispersants, comprenant:
    a. un dispersant avec un rapport carbonyle sur azote de 1 ou plus; et
    b. un dispersant avec un rapport carbonyle sur azote de moins de 1;
    où le rapport du dispersant avec le rapport carbonyle sur azote de 1 ou plus sur le dispersant avec le rapport carbonyle sur azote de moins de 1 est de 1:1 à 15:1;
    (c) un système d'antioxydants, comprenant:
    a. un phénol encombré;
    (d) une huile à viscosité lubrifiante; et
    (e) un modificateur de viscosité où le modificateur de viscosité est un mélange de deux copolymères dérivés de (A) un copolymère comprenant de 45 à 85 pour cent en poids de motifs dérivés d'éthylène, ayant un M w de 50 000 à 300 000, un M w/M n de moins de 3 et un point de fusion de 0 °C à 60 °C; et (B) un copolymère bloc comprenant un motif comonomère vinylaromatique et un deuxième motif comonomère;
    dans laquelle la composition a une teneur en phosphore inférieure ou égale à 800 ppm; et dans laquelle la teneur en cendre sulfatée est inférieure ou égale à 1,1 pour cent en poids de la composition.
  2. Composition selon la revendication 1, comprenant en outre un tensioactif autre que le composant (a)(i).
  3. Composition selon la revendication 1, comprenant en outre un antioxydant de type diphénylamine, un dithiocarbamate de molybdène, une oléfine sulfurée ou des mélanges de ceux-ci.
  4. Composition selon la revendication 1, comprenant en outre un ester borique.
  5. Composition selon la revendication 2, dans laquelle ledit tensioactif autre que le composant (a)(i) est choisi dans le groupe consistant en un sulfonate, un phénate, un phénate sulfuré, un carboxylate, un phosphate, une saligénine et un salicylate d'alkyle.
  6. Composition selon la revendication 5, dans laquelle ledit tensioactif autre que le composant (a)(i) est sous la forme d'un sel métallique.
  7. Composition selon la revendication 6, dans laquelle ledit sel métallique est un sel de métal alcalino-terreux.
  8. Composition selon la revendication 7, dans laquelle ledit sel métallique est présent à raison de 550 ppm ou moins.
  9. Composition selon la revendication 8, dans laquelle ledit sel métallique est un sel de calcium ou magnésium.
  10. Composition selon la revendication 2, dans laquelle ledit tensioactif autre que le composant (a)(i) est une saligénine de magnésium, une saligénine de calcium, un sulfonate de magnésium, un sulfonate de calcium ou des mélanges de ceux-xi.
  11. Composition selon la revendication 1, comprenant en outre un hydrocarbyl-dithiophosphate métallique.
  12. Composition selon la revendication 1, dans laquelle le rapport TBN/TAN pour le mélange des dispersants est de 3: 1 à 7: 1.
  13. Procédé pour la préparation d'une composition, comprenant l'étape consistant à mélanger:
    (a) de 0,01 à 20 pour cent en poids, sur produit sans huile et par rapport au poids de la composition, d'un système de tensioactifs, comprenant:
    (i) de 0,25 à 4 pour cent en poids de la composition d'un salixarate métallique; et
    (ii) éventuellement un tensioactif autre que le composant (a)(i);
    (b) de 0,01 à 30 pour cent en poids, sur produit sans huile et par rapport au poids de la composition, d'un système de dispersants, comprenant:
    a. un dispersant avec un rapport carbonyle sur azote de 1 ou plus; et
    b. un dispersant avec un rapport carbonyle sur azote de moins de 1;
    où le rapport du dispersant avec le rapport carbonyle sur azote de 1 ou plus sur le dispersant avec le rapport carbonyle sur azote de moins de 1 est de 1:1 à 15:1;
    (c) un système d'antioxydants, comprenant:
    a. un phénol encombré;
    (d) une huile à viscosité lubrifiante; et
    (e) un modificateur de viscosité où le modificateur de viscosité est un mélange de deux copolymères dérivés de (A) un copolymère comprenant de 45 à 85 pour cent en poids de motifs dérivés d'éthylène, ayant un M w de 50 000 à 300 000, un M w/M n de moins de 3 et un point de fusion de 0 °C à 60 °C; et (B) un copolymère bloc comprenant un motif comonomère vinylaromatique et un deuxième motif comonomère;
    dans laquelle la composition a une teneur en phosphore inférieure ou égale à 800 ppm; et dans laquelle la teneur en cendre sulfatée est inférieure ou égale à 1,1 pour cent en poids de la composition.
  14. Procédé selon la revendication 13, dans lequel le rapport du dispersant avec le rapport carbonyle sur azote de 1 ou plus sur le dispersant avec le rapport carbonyle sur azote de moins de 1 est de 2:1 à 10:1.
  15. Utilisation de la composition selon l'une quelconque des revendications 1 à 12 pour fournir au moins une ou plusieurs d'une propreté de moteur améliorée, d'une action détergente améliorée, d'une formation de boue réduite, d'une usure réduite, d'une formation de surfaces-miroir (bore polishing) réduite et d'une consommation d'huile réduite.
EP04813239A 2003-12-12 2004-12-07 Composition lubrifiante contenant de dispersants succinimide Not-in-force EP1692249B1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP10152942A EP2184338A3 (fr) 2003-12-12 2004-12-07 Composition lubrifiante contenant des sels métalliques de salixarate comme détergents et de succinimides comme dispersants

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US52898903P 2003-12-12 2003-12-12
PCT/US2004/040895 WO2005061682A2 (fr) 2003-12-12 2004-12-07 Composition lubrifiante contenant de dispersants succinimide

Publications (2)

Publication Number Publication Date
EP1692249A2 EP1692249A2 (fr) 2006-08-23
EP1692249B1 true EP1692249B1 (fr) 2010-02-24

Family

ID=34710107

Family Applications (2)

Application Number Title Priority Date Filing Date
EP04813239A Not-in-force EP1692249B1 (fr) 2003-12-12 2004-12-07 Composition lubrifiante contenant de dispersants succinimide
EP10152942A Withdrawn EP2184338A3 (fr) 2003-12-12 2004-12-07 Composition lubrifiante contenant des sels métalliques de salixarate comme détergents et de succinimides comme dispersants

Family Applications After (1)

Application Number Title Priority Date Filing Date
EP10152942A Withdrawn EP2184338A3 (fr) 2003-12-12 2004-12-07 Composition lubrifiante contenant des sels métalliques de salixarate comme détergents et de succinimides comme dispersants

Country Status (7)

Country Link
EP (2) EP1692249B1 (fr)
JP (1) JP2007514040A (fr)
AT (1) ATE458800T1 (fr)
AU (1) AU2004303846B2 (fr)
CA (1) CA2549095C (fr)
DE (1) DE602004025731D1 (fr)
WO (1) WO2005061682A2 (fr)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2648996T3 (es) * 2004-12-22 2018-01-09 The Lubrizol Corporation Método de control de la viscosidad
US8759262B2 (en) 2005-12-28 2014-06-24 Infineum International Limited Lubricating oil compositions
EP1803793B1 (fr) * 2005-12-28 2015-06-17 Infineum International Limited Composiitons d'huile lubrifiante
JP2009543939A (ja) * 2006-07-17 2009-12-10 ザ ルブリゾル コーポレイション 潤滑油組成物および内燃エンジンの排出制御システムの効率を向上させる方法
JP2011508810A (ja) * 2007-12-27 2011-03-17 ザ ルブリゾル コーポレイション 界面活性剤を含む潤滑組成物
CA2813585A1 (fr) 2010-10-06 2012-04-12 The Lubrizol Corporation Composition d'huile lubrifiante comportant un additif antibuee
US9528068B2 (en) 2011-02-17 2016-12-27 The Lubrizol Corporation Lubricants with good TBN retention
FR2980799B1 (fr) * 2011-09-29 2013-10-04 Total Raffinage Marketing Composition lubrifiante pour moteur marin
KR102603891B1 (ko) * 2015-03-31 2023-11-17 이데미쓰 고산 가부시키가이샤 가솔린 엔진용 윤활유 조성물 및 그의 제조 방법
CN109715770B (zh) * 2016-07-15 2023-05-26 路博润公司 用于硅氧烷沉积物控制的发动机润滑剂
CN110799632B (zh) * 2017-07-11 2022-05-03 株式会社Adeka 使有机钼化合物在基油中的分散性长期稳定化的方法

Family Cites Families (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL124842C (fr) 1959-08-24
US3381022A (en) 1963-04-23 1968-04-30 Lubrizol Corp Polymerized olefin substituted succinic acid esters
US3401118A (en) 1967-09-15 1968-09-10 Chevron Res Preparation of mixed alkenyl succinimides
US3634515A (en) 1968-11-08 1972-01-11 Standard Oil Co Alkylene polyamide formaldehyde
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
US4594378A (en) 1985-03-25 1986-06-10 The Lubrizol Corporation Polymeric compositions, oil compositions containing said polymeric compositions, transmission fluids and hydraulic fluids
US6077455A (en) * 1995-07-17 2000-06-20 Exxon Chemical Patents Inc Automatic transmission fluid of improved viscometric properties
US5747433A (en) 1996-07-15 1998-05-05 The Lubrizol Corporation Oil concentrates of polymers with improved viscosity
US5741764A (en) * 1996-10-15 1998-04-21 The Lubrizol Corporation Two-cycle lubricant containing solvent and high molecular weight polymer
US6165235A (en) 1997-08-26 2000-12-26 The Lubrizol Corporation Low chlorine content compositions for use in lubricants and fuels
WO1999025677A1 (fr) 1997-11-13 1999-05-27 Lubrizol Adibis Holdings (Uk) Limited Calixarenes salicycliques et leur utilisation comme additifs pour lubrifiants
EA200000515A1 (ru) 1997-11-13 2000-12-25 Бп Ойл Интернэшнл Лимитед Топливная композиция и смесь
US6124249A (en) 1998-12-22 2000-09-26 The Lubrizol Corporation Viscosity improvers for lubricating oil compositions
US6008165A (en) 1998-07-31 1999-12-28 The Lubrizol Corporation Alcohol borate esters and borated dispersants to improve bearing corrosion in engine oils
WO2001056968A1 (fr) 2000-02-07 2001-08-09 Bp Oil International Limited Calixarenes et leur utilisation en tant qu'additifs de lubrification
US6310009B1 (en) * 2000-04-03 2001-10-30 The Lubrizol Corporation Lubricating oil compositions containing saligenin derivatives
US6610637B2 (en) * 2001-02-13 2003-08-26 The Lubrizol Corporation Synthetic diesel engine lubricants containing dispersant-viscosity modifier and functionalized phenol detergent
EP1401991A2 (fr) * 2001-06-29 2004-03-31 The Lubrizol Corporation Lubrifiant a base d'eau en emulsion de type huileux avec base solide en suspension
WO2003002697A1 (fr) * 2001-06-29 2003-01-09 The Lubrizol Corporation Lubrifiant comprenant une base dispersible dans l'eau
ATE298362T1 (de) * 2001-08-24 2005-07-15 Lubrizol Corp Lineare verbindungen enthaltend phenol und salicylsäure-einheiten
US6583092B1 (en) * 2001-09-12 2003-06-24 The Lubrizol Corporation Lubricating oil composition
US7407919B2 (en) * 2001-11-05 2008-08-05 The Lubrizol Corporation Sulfonate detergent system for improved fuel economy
EP1497399B1 (fr) * 2002-04-19 2018-08-15 The Lubrizol Corporation Composition de lubrifiant qui convient pour des moteurs deux temps balayes par carter, a injection directe
ES2584163T3 (es) 2003-03-28 2016-09-26 The Lubrizol Corporation Composiciones mejoradoras de la viscosidad que proporcionan al aceite lubricante características mejoradas a baja temperatura

Also Published As

Publication number Publication date
AU2004303846A1 (en) 2005-07-07
CA2549095A1 (fr) 2005-07-07
WO2005061682A3 (fr) 2005-10-27
WO2005061682A2 (fr) 2005-07-07
CA2549095C (fr) 2013-05-21
EP2184338A2 (fr) 2010-05-12
ATE458800T1 (de) 2010-03-15
EP1692249A2 (fr) 2006-08-23
DE602004025731D1 (de) 2010-04-08
AU2004303846B2 (en) 2009-10-29
JP2007514040A (ja) 2007-05-31
EP2184338A3 (fr) 2010-08-11

Similar Documents

Publication Publication Date Title
EP3153568B1 (fr) Concentrés d'additif pour la formulation de compositions d'huile lubrifiante
EP3024916B1 (fr) Composition lubrifiante contenant un hydrocarbylphénol alcoxylé
US9765275B2 (en) Composition containing ester compounds and a method of lubricating an internal combustion engine
EP2545148B1 (fr) Composés et complexes de titane et molybdène utilisés comme additifs dans des lubrifiants
EP1692249B1 (fr) Composition lubrifiante contenant de dispersants succinimide
CA2710757A1 (fr) Composition lubrifiante contenant du detergent surbasique
US20060276351A1 (en) Molybdenum-containing lubricant for improved power or fuel economy
JP2011214013A (ja) Ｚｄｄｐを実質的に含まない潤滑組成物
EP3911724B1 (fr) Huiles moteur pour la manipulation de suie et la réduction de frottement
EP1567624B1 (fr) Lubrifiant contenant du molybdene destine a ameliorer la puissance ou a economiser du carburant
CN111479908A (zh) 烷基酚清洁剂
US11898119B2 (en) Lubricating oil compositions with resistance to engine deposit and varnish formation
US20230193151A1 (en) Lubricating oil composition having resistance to engine deposits
EP4368689A1 (fr) Tensioactifs polymeres pour proprietes d'emulsion et d'ecoulement ameliorees a basses temperatures
US20240209277A1 (en) Detergent- free and low- ash lubricating composition
EP3882330A1 (fr) Composition d'huile lubrifiante à faible viscosité
WO2024137363A1 (fr) Composition lubrifiante sans détergent et à faible teneur en cendres
CN115038777A (zh) 用于生产烷基水杨酸的方法和由其衍生的高碱性洗涤剂

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: 20060627

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU MC NL PL PT RO SE SI SK TR

17Q First examination report despatched

Effective date: 20061002

DAX Request for extension of the european patent (deleted)
GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU MC NL PL PT RO SE SI SK TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REF Corresponds to:

Ref document number: 602004025731

Country of ref document: DE

Date of ref document: 20100408

Kind code of ref document: P

REG Reference to a national code

Ref country code: NL

Ref legal event code: VDEP

Effective date: 20100224

LTIE Lt: invalidation of european patent or patent extension

Effective date: 20100224

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

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100624

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100224

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100625

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

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100224

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100224

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100224

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100224

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

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100224

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100224

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100224

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100525

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100604

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100224

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100224

Ref country code: BE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100224

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

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100224

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100224

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100524

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

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

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100224

26N No opposition filed

Effective date: 20101125

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

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100224

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

Ref country code: GB

Payment date: 20101229

Year of fee payment: 7

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

Ref country code: MC

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

Effective date: 20101231

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

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

Ref country code: IE

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

Effective date: 20101207

Ref country code: CH

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

Effective date: 20101231

Ref country code: LI

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

Effective date: 20101231

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

Ref country code: DE

Payment date: 20111229

Year of fee payment: 8

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

Ref country code: LU

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

Effective date: 20101207

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100825

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

Ref country code: TR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20100224

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

Effective date: 20121207

REG Reference to a national code

Ref country code: DE

Ref legal event code: R119

Ref document number: 602004025731

Country of ref document: DE

Effective date: 20130702

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: 20130702

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: 20121207

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 12

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 13

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 14

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

Ref country code: FR

Payment date: 20191226

Year of fee payment: 16

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: 20201231