WO1996037582A1 - Lubricating oil composition - Google Patents
Lubricating oil composition Download PDFInfo
- Publication number
- WO1996037582A1 WO1996037582A1 PCT/US1995/006620 US9506620W WO9637582A1 WO 1996037582 A1 WO1996037582 A1 WO 1996037582A1 US 9506620 W US9506620 W US 9506620W WO 9637582 A1 WO9637582 A1 WO 9637582A1
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- WIPO (PCT)
- Prior art keywords
- weight
- composition
- carbon atoms
- alkyl group
- lubricating oil
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- 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
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- 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
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/26—Carboxylic acids; Salts thereof
- C10M129/48—Carboxylic acids; Salts thereof having carboxyl groups bound to a carbon atom of a six-membered aromatic ring
- C10M129/54—Carboxylic acids; Salts thereof having carboxyl groups bound to a carbon atom of a six-membered aromatic ring containing hydroxy groups
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- 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
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/52—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of 30 or more atoms
- C10M133/56—Amides; Imides
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- 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
- C10M135/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
- C10M135/12—Thio-acids; Thiocyanates; Derivatives thereof
- C10M135/14—Thio-acids; Thiocyanates; Derivatives thereof having a carbon-to-sulfur double bond
- C10M135/18—Thio-acids; Thiocyanates; Derivatives thereof having a carbon-to-sulfur double bond thiocarbamic type, e.g. containing the groups
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M137/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
- C10M137/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having no phosphorus-to-carbon bond
- C10M137/04—Phosphate esters
- C10M137/10—Thio derivatives
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M141/00—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
- C10M141/10—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic phosphorus-containing compound
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- C10M159/00—Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
- C10M159/12—Reaction products
- C10M159/20—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products
- C10M159/22—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products containing phenol radicals
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- 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
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- 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
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- C10M2207/146—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings having carboxyl groups bound to carbon atoms of six-membeered aromatic rings having a hydrocarbon substituent of thirty or more carbon atoms
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- C10M2207/26—Overbased carboxylic acid salts
- C10M2207/262—Overbased carboxylic acid salts derived from hydroxy substituted aromatic acids, e.g. salicylates
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
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- C10M2215/086—Imides
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- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/046—Polyamines, i.e. macromoleculars obtained by condensation of more than eleven amine monomers
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- C10M2217/06—Macromolecular compounds obtained by functionalisation op polymers with a nitrogen containing compound
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- C10M2219/06—Thio-acids; Thiocyanates; Derivatives thereof
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- C10M2219/066—Thiocarbamic type compounds
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- C10M2219/068—Thiocarbamate metal salts
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- 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
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- C10M2223/04—Phosphate esters
- C10M2223/045—Metal containing thio derivatives
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- C10M2227/06—Organic compounds derived from inorganic acids or metal salts
- C10M2227/061—Esters derived from boron
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- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
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- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/02—Bearings
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- C10N2040/046—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for traction drives
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- C10N2040/251—Alcohol fueled engines
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- C10N2040/28—Rotary engines
Definitions
- the present invention relates to a novel lubricating oil composi ⁇ tion. More specifically, the present invention relates to a lubricating oil composition having excellent antiwear properties and friction-reducing properties, capable of maintaining the friction-reducing properties, for a prolonged period of time, useful as a lubricating oil for internal-combustion engines, automatic transmission gearboxes, dampers, power steering units and the like, particularly useful as a lubricating oil for internal-combustion engines.
- Lubricating oils have been used for internal-combustion engines, and for driving units and gears such as automatic transmission gearboxes, dampers and power steerings in order to smoothly operate them.
- lubricating oils for internal-combustion engines not only lubricate various sliding portions, but also cool the inside of the engines, clean and disperse those products which are produced by combustion, and furthermore prevent the rusting and corrosion of the engines.
- lubricating oils ensure the smooth operation of the engines under all operating conditions to prevent the wear and seizure of the engines.
- the lubricated parts of the engines are, in most cases, under the fluid lubrication condition.
- valve-trains and the top and bottom dead centers of a piston tend to be under the boundary lubrication condition.
- Antiwear properties under the boundary lubrication condition are generally imparted by the addition of zinc dithiophosphate or zinc dithio ⁇ carbamate.
- a friction modifier is added to lubricating oils.
- an extreme pressure agent such as a molybdenum compound or a phosphoric ester, or a compound which is an oily agent such as a fatty ester or an alkylamine has been generally used as the friction modifier.
- the present invention has accomplished the objective of develop ⁇ ing a lubricating oil (engine oil) which can maintain the effect of reducing friction in engines for a long period of time under these circumstances.
- a lubricating oil composition having the above described properties is obtained by blending, sulfoxymolybdenum dithio ⁇ carbamate having a specific alkyl group, zinc dialkyldithiophosphate having a specific alkyl group, zinc dialkyldithiophosphate having a specific alkyl group, specific alkylsalicylate(s), and, if desired, succmimide containing boron, each in a predetermined amount intra lubricating oil base stock.
- the present invention has been accomplished on the basis of the above finding.
- the present invention relates to the following lubricating oil compositions:
- a lubricating oil composition characterized by comprising a lubricating base oil and additives consisting essentially of:
- sulfoxymolybdenum dithiocarbamate containing a hydro ⁇ carbon group having 8 to 18 carbon atoms (b) zinc dialkyldithiophosphate selected from the group consist ⁇ ing of zinc dialkyldithiophosphate containing a primary alkyl group having 1 to 18 carbon atoms, and a mixture of zinc dialkyldithiophosphate containing a primary alkyl group having 1 to 18 carbon atoms and zinc dialkyldithiophosphate containing a secondary alkyl group having 1 to 18 carbon atoms, and
- the amount of molybdenum derived from the sulfoxymolybdenum dithiocarbamate being from 200 to 1000 ppm (weight basis) of the total weight of the composition
- the amount of phosphorus derived from the zinc dialkyldithio ⁇ phosphate being from 0.04 to 0.15% by weight of the total weight of the composition
- the total amount of the calcium alkylsalicylate and the magnesium alkylsalicylate being from 1 to 10% by weight of the total weight of the composition
- a lubricating oil composition characterized by comprising a lubricating base oil and additives consisting essentially of:
- zinc dialkyldithiophosphate selected from the group consisting of zinc dialkyldithiophosphate containing a primary alkyl group having 1 to 18 carbon atoms, and a mixture of zinc dialkyldithiophosphate containing a primary alkyl group having 1 to 18 carbon atoms and zinc dialkyl ⁇ dithiophosphate containing a secondaiy alkyl group having 1 to 18 carbon atoms,
- the amount of molybdenum derived from the sulfoxymolybdenum dithiocarbamate being from 200 to 1000 ppm (weight basis) of the total weight of the composition
- the amount of phosphorus derived from the zinc dialkyldithio ⁇ phosphate being from 0.04 to 0.15% by weight of the total weight of the composition
- the total amount of the calcium alkylsalicylate and the magnesium alkylsalicylate being from 1 to 10% by weight of the total weight of the composition
- the amount of boron derived from the succirtimide containing boron being from 0.005 to 0.06% by weight of the total weight of the composition.
- lubricating base stock oil which is used in the lubricating oil composition of the present invention
- any base oil such as mineral oil or synthetic oil, which is commonly used for the conventional lubricating basic oils can be used.
- Examples of the mineral oil include raffinates which can be obtained by subjecting raw materials for lubricating oils to solvent refining, using an aromatic extraction solvent such as phenol or furfural, hydrogenated oils which can be obtained by subjecting raw materials for lubricating oils to hydrogenation treatment, using a hydrogenation catalyst such as cobalt or molybdenum with a silica-alumina carrier, and lubricating oil fractions which can be obtained by the isomerization of waxes.
- Suitable base stocks include 60 neutral oil, 100 neutral oil, 150 neutral oil, 300 neutral oil, 500 neutral oil and bright stocks.
- Examples of the synthetic oil include poly alpha-olefin oligomers, polybutenes, alkylbenzenes, polyol esters, polyglycol esters, dibasic esters, phosphoric esters and silicone oils. These base oils belonging to mineral oil or synthetic oil can be used either singly or in combination of two or more. Further, a mixture of mineral oil and synthetic oil can also be used.
- oils which have a viscosity at 100°C of 3 to 20 cSt are preferable as the base oils for use in the lubricating oil composition of the present invention.
- hydrocracked oils and wax-isomerized oils which contain 3% by weight or less of aromatics, 50 ppm or less of sulfur and 50 ppm or less of nitrogen are particularly preferred.
- Examples of the hydrocarbon group having 8 to 18 carbon atoms, represented by R and R ⁇ in the general formula [I] include hydrocarbon groups such as an alkyl group having 8 to 18 carbon atoms, an alkenyl group having 8 to 18 carbon atoms, a cycloalkyl group having 8 to 18 carbon atoms, an aryl group having 8 to 18 carbon atoms, an alkylaryl group and an arylalkyl group.
- the above alkyl and alkenyl groups may be linear or branched.
- the hydro ⁇ carbon group represented by R ⁇ and R ⁇ have 8 carbon atoms.
- hydrocarbon group represented by R* and R2 include octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, octenyl, noneyl, decenyl, undecenyl, dodecenyl, tridecenyl, tetradecenyl, hexadecenyl, octadecenyl, dimethylcyclohexyl, ethylcyclohexyl, methylcyclohexylmethyl, cyclohexylethyl, propylcyclohexyl, butylcyclohexyl, heptylcyclohexyl, di- methylphenyl, methylbenzyl, phenethyl, naphthyl and dimethylnaphthyl groups.
- sulfoxymolybdenum dithiocarbamates can be used. Further, the sulfoxymolybdenum dithiocarbamate is incorporated into the composition so that the amount of molybdenum derived from the sulfoxymolybdenum dithio ⁇ carbamate can be from 200 to 1000 ppm (weight basis), preferably from 300 to 800 ppm (weight basis) of the total weight of the composition.
- the sulfoxymolybdenum dithiocarbamate When the sulfoxymolybdenum dithiocarbamate is incorporated in such an amount that the amount of molybdenum derived from the sulfoxymolybdenum dithiocarbamate is less than 200 ppm (weight basis) of the total weight of the composition, the effect of improving friction-reducing properties cannot be sufficiently obtained.
- R-* and R ⁇ are independently a primary and secondary alkyl group with 1 to 18, preferably 3 to 18 carbon atoms and may or may not be the same.
- any of the following ones can be used as the zinc dialkyldithiophosphate: zinc dialkyl ⁇ dithiophosphate represented by the general formula [2] in which all of the alkyl groups are primary; a mixture of zinc dialkyldithiophosphate in which all of the alkyl groups are primary and zinc dialkyldithiophosphate in which all of the alkyl groups is primary and the other alkyl group is secondary; zinc dialkyl ⁇ dithiophosphate in which one of the alkyl groups are secondary; and a mixture thereof.
- the primary and secondary alkyl groups represented by R ⁇ and R ⁇ in the general formula [2] are propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl and dodecyl groups.
- zinc dialkyldithiophosphate containing a primary or secondary alkyl group having 3 to 12 carbon atoms is preferably used in the lubricating oil composition of the present invention.
- the zinc dialkyldithiophosphate is incorporated so that the amount of phosphorus derived from the zinc dialkyldithiophosphate can be from 0.04 to 0.15% by weight, preferably from 0.06 to 0.12% by weight of the total weight of the composition.
- the zinc dialkyldithiophosphate is incorporated into the composition in such an amount that the amount of phosphorus derived from the zinc dialkyl ⁇ dithiophosphate is less than 0.04% by weight of the total weight of the composition, the resulting composition is poor in antiwear properties, in addi ⁇ tion, cannot have a satisfactorily low coefficient of friction under the operating conditions of high oil temperatures and low rotational speeds.
- M is calcium or magnesium
- R ⁇ and R ⁇ are independently alkyl group with 8 to 30 carbon atoms and may or may not be the same.
- the alkyl group having 8 to 30 carbon atoms represented by R ⁇ and R6 in the general formula [3] may be linear, branched or cyclic one.
- Examples of such an alkyl group include octyl, nonyl, decyl, dodecyl, pentadecyl, octadecyl, eicosyl, docosyl, tricosyl, hexacosyl, triacontyl, dimethylcyclohexyl, ethylcyclohexyl, methylcyclohexylmethyl and cyclo- hexylefhyl groups.
- the alkylsalicylate is incorporated as a mixture of 100 to 50% by weight of calcium alkylsalicylate and 0 to 50% by weight of magnesium alkylsalicylate.
- the mixture is incorporated in such an amount that the total amount of the calcium alkylsalicylate and the magnesium alkylsalicylate is from 0.5 to 10% by weight, preferably from 1 to 6% by weight of the total weight of the composition.
- the total amount of the calcium alkylsalicylate and the magnesium alkylsalicylate is less than 0.5% by weight of the total weight of the composition, cleaning effect cannot be sufficiently obtained.
- the total base number of the composition it is preferable to adjust the total base number of the composition to 3 to 10, preferably 4 to 7.
- the base number of the composition can be determined in accordance with RS K2501.
- the total base number of the composition can be adjusted by selecting calcium alkylsalicylate and magnesium alkylsalicylate, each having a proper base number.
- Succmimide containing boron can be incorporated into the lubricating oil composition of the present invention, if desired.
- the boron/nitrogen ratio regarding the number of the atoms contained in the succinimide containing boron which is used in the lubricating oil composition of the present invention is from 0.05 to 1.5, preferably from 0.1 to 0.8.
- the boron/nitrogen ratio is less than 0.05, the resulting composition cannot have sufficiently-improved friction-reducing properties.
- the boron/nitrogen ratio exceeds 1.5, the friction-reducing properties of the resulting composition are impaired.
- the succinimide containing boron is incorporated so that the amount of boron derived from the succmimide containing boron can be from 0.005 to 0.06% by weight, preferably from 0.01 to 0.04% by weight of the total weight of the composition.
- the succinimide containing boron is used in such an amount that the amount of boron derived from the succinimide containing boron is less than 0.005% by weight of the total weight of the composition, the resulting composition cannot have sufficiently-improved friction-reducing properties.
- additives which have been usually incorporated into the conventional lubricating oils, such as a metallic detergent, another friction modifier, an antioxidant, a viscosity index improver, a pour point depressant, an anti-foaming agent, other antiwear agent(s), a rust preventive, an ashless dispersant and a corrosion inhibitor, can be added, if necessary, to the lubricating oil composition of the present invention within such a limit that the object of the present invention can be fully attained.
- a metallic detergent such as a metallic detergent, another friction modifier, an antioxidant, a viscosity index improver, a pour point depressant, an anti-foaming agent, other antiwear agent(s), a rust preventive, an ashless dispersant and a corrosion inhibitor
- the metallic detergent examples include calcium sulfonate, magnesium sulfonate, barium sulfonate, calcium phenate, barium phenate, calcium salicylate and magnesium salicylate.
- the metallic detergent is used in the composition in an amount of 0.1 to 5% by weight.
- Examples of the friction modifier include partial esters of poly ⁇ valent alcohols, amines, amides and ester sulfides.
- examples of the antioxidant include amine antioxidants such as alkylated diphenylamines, phenyl-alpha-naphthylamines and alkylated alpha- naphmylamines, and phenolic antioxidants such as 2,6-di-t-butyl-4-methylphenol and 4,4'-methylene-bis(2,6-di-t-butylphenol). In general, such an antioxidant is used in the composition in an amount of 0.05 to 2% by weight.
- viscosity index improver examples include those of poly- methacrylate type, polyisobutylene type, ethylene-propylene copolymer type and stryene-butadiene hydrogenated copolymer type. In general, such an improver is used in the composition in an amount of 0.5 to 35% by weight.
- pour point depressant examples include polyalkyl- mefhacrylate, a condensation product of chlorinated paraffin and naphthalene and alkylated polystyrene.
- anti-foaming agent examples include dimethyl polysiloxane and polyacrylic acid.
- antiwear agent examples include metallic salts of thiophosphoric acid, metallic salts of thiocarbamic acid, sulfur compounds, phosphoric esters and phosphorous esters. In general, this agent is used in the composition in an amount of 0.05 to 5.0% by weight.
- rust preventive additive examples include fatty acids, partial esters of alkenyl succinates, fatty acid soaps, alkylsulfonates, fatty polyvalent alcohol esters, fatty amines, paraffin oxides and alkyl polyoxyethylene ethers.
- ashless dispersant examples include those of succinimide type, succinamide type, benzylamine type and ester type. In general, such a dispersant is used in the composition in an amount of 0.5 to 7% by weight.
- the coefficients of friction of the lubricating oil compositions were determined by a reciprocating sliding friction tester [SRV Friction Tester] under the conditions of a frequency of 50 Hz, an amplitude of 3 mm, a load of 25 N, a temperature of 80°C and a test time of 25 minutes.
- the lubricating oil compositions of these examples are those which contain sulfoxymolybdenum dithiocarbamate, zinc dialkyldithiophosphate and alkylsalicylate.
- Each lubricating oil composition was prepared by blending the components whose type and amount are shown in Table 1 with a base oil (100 neutral oil having a viscosity at 100°C of 4.4 mm/s ⁇ ). The coefficient of friction of each composition thus obtained was determined right after the composition was prepared, and after the composition was oxidized by being held at 150°C for 72 hours. The results are shown in Table 1.
- the lubricating oil compositions of these examples are those which contain sulfoxymolybdenum dithiocarbamate, zinc dialkyldithiophosphate, alkyl ⁇ salicylate and succinimide containing boron.
- Each lubricating oil composition was prepared by blending the components whose type and amount are shown in Table 2 with a base oil (100 neutral oil having a viscosity at 100°C of 4.4 mm/s2). The coefficient of friction of each composition thus obtained was determined right after the composition was prepared, and after the composition was oxidized by being held at 150°C for 72 hours. The results are shown in Table 2. TABLE 2
- the lubricating oil compositions of Examples 10 to 18 according to the present invention into which succmimide containing boron was incorporated, had a coefficient of friction lower than that of any of the lubricat ⁇ ing oil compositions of Examples 1 to 9 which contain no succinimide contain ⁇ ing boron, and showed excellent friction-reducing properties. Moreover, almost no change was found in the coefficient of friction even after the compositions were heated at 150°C for 72 hours and oxidized. Therefore, it can be seen that the lubricating oil compositions of the present invention are excellent in heat resistance.
- the lubricating oil compositions of the present invention prepared by blending sulfoxymolybdenum dithiocarbamate having a specific structure, zinc dialkyldithiophosphate, alkylsalicylate, and, if desired, succinimide contain ⁇ ing boron with a base oil, therefore, have excellent antiwear properties, can maintain friction-reducing properties for a prolonged period of time, and are excellent in both friction-reducing properties and heat resistance.
- the lubricat ⁇ ing oil compositions of the present invention are thus useful as lubricating oils for internal-combustion engines, automatic transmission gearboxes, dampers, power steering units and the like, particularly useful as lubricating oils for internal-combustion engines.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
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Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6131165A JPH07316577A (en) | 1994-05-20 | 1994-05-20 | Lubricant oil composition |
PCT/US1995/006620 WO1996037582A1 (en) | 1994-05-20 | 1995-05-24 | Lubricating oil composition |
CA002218811A CA2218811C (en) | 1994-05-20 | 1995-05-24 | Lubricating oil composition |
EP95920657A EP0847435A4 (en) | 1995-05-24 | 1995-05-24 | Lubricating oil composition |
US08/945,705 US6855675B1 (en) | 1995-05-24 | 1995-05-24 | Lubricating oil composition |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6131165A JPH07316577A (en) | 1994-05-20 | 1994-05-20 | Lubricant oil composition |
PCT/US1995/006620 WO1996037582A1 (en) | 1994-05-20 | 1995-05-24 | Lubricating oil composition |
CA002218811A CA2218811C (en) | 1994-05-20 | 1995-05-24 | Lubricating oil composition |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1996037582A1 true WO1996037582A1 (en) | 1996-11-28 |
Family
ID=27170497
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1995/006620 WO1996037582A1 (en) | 1994-05-20 | 1995-05-24 | Lubricating oil composition |
Country Status (3)
Country | Link |
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JP (1) | JPH07316577A (en) |
CA (1) | CA2218811C (en) |
WO (1) | WO1996037582A1 (en) |
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EP0953629A1 (en) * | 1998-05-01 | 1999-11-03 | Shell Internationale Researchmaatschappij B.V. | Lubricating oil compositions for internal combustion engines |
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WO2000063325A1 (en) * | 1999-04-14 | 2000-10-26 | Shell Internationale Research Maatschappij B.V. | Hydraulic fluid |
US6140282A (en) * | 1999-12-15 | 2000-10-31 | Exxonmobil Research And Engineering Company | Long life lubricating oil composition using particular detergent mixture |
US6191081B1 (en) | 1999-12-15 | 2001-02-20 | Exxonmobil Research And Engineering Company | Long life medium and high ash oils with enhanced nitration resistance |
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EP1329496A1 (en) * | 2002-01-14 | 2003-07-23 | Infineum International Limited | Lubricating oil compositions with low sulfur and phosphorous content |
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AU750716B2 (en) * | 1998-05-01 | 2002-07-25 | Shell Internationale Research Maatschappij B.V. | Lubricating oil composition for internal combustion engines |
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Also Published As
Publication number | Publication date |
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CA2218811C (en) | 2006-02-07 |
CA2218811A1 (en) | 1996-11-28 |
JPH07316577A (en) | 1995-12-05 |
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