US20050148477A1 - Lubricating composition substantially free of ZDDP - Google Patents

Lubricating composition substantially free of ZDDP Download PDF

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Publication number
US20050148477A1
US20050148477A1 US10/751,809 US75180904A US2005148477A1 US 20050148477 A1 US20050148477 A1 US 20050148477A1 US 75180904 A US75180904 A US 75180904A US 2005148477 A1 US2005148477 A1 US 2005148477A1
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Prior art keywords
composition
group
metal
oil
hydrocarbyl
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US10/751,809
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Inventor
Christopher Friend
Rodney McAtee
Michael Sutton
David Cressey
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Lubrizol Corp
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Lubrizol Corp
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Priority to US10/751,809 priority Critical patent/US20050148477A1/en
Assigned to THE LUBRIZOL CORPORATION reassignment THE LUBRIZOL CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: MCATEE, RODNEY J., SUTTON, MICHAEL, CRESSEY, DAVID, FRIEND, CHRISTOPHER L.
Priority to JP2006547216A priority patent/JP2007517937A/ja
Priority to CA002552606A priority patent/CA2552606A1/en
Priority to EP04814892.8A priority patent/EP1702049B1/en
Priority to PCT/US2004/042758 priority patent/WO2005068590A1/en
Publication of US20050148477A1 publication Critical patent/US20050148477A1/en
Priority to JP2011165988A priority patent/JP2011214013A/ja
Abandoned legal-status Critical Current

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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
    • 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
    • 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
    • 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
    • C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl 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
    • C10M2207/02—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
    • 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
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28—Esters
    • C10M2207/287—Partial esters
    • C10M2207/288—Partial esters containing free carboxyl 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
    • C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/08—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
    • C10M2209/086—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type polycarboxylic, e.g. maleic acid
    • 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
    • C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
    • 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
    • C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/064—Di- and triaryl amines
    • 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
    • C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
    • 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
    • C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2217/06—Macromolecular compounds obtained by functionalisation op polymers with a nitrogen containing compound
    • 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
    • C10N2030/04—Detergent property or dispersant property
    • 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
    • C10N2030/06—Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
    • 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
    • C10N2030/50—Emission or smoke controlling properties
    • 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

Definitions

  • the present invention relates to a lubricating oil composition containing a metal salixarate and other performance additives.
  • the lubricating oil composition has antiwear and detergency performance in the absence of a metal hydrocarbyl dithiophosphate.
  • 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, 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 greenhouse gases 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.
  • U.S. Pat. NO. 6,200,936 discloses compounds containing phenolic units and salicylic units in a lubricating composition.
  • the compounds can be salted with calcium.
  • the examples of lubricating compositions contain phenolic units with a dodecyl alkyl group.
  • the compounds of the invention can be used as a detergent in gasoline or diesel fuel. They also stabilise gasoline or diesel compositions against thermal decomposition.
  • WO99/25793 discloses a fuel composition containing kerosene and compounds containing phenolic units and salicylic units.
  • the compounds can be salted with calcium.
  • the examples of lubricating compositions contain phenolic units with a dodecyl alkyl group.
  • European Patent Application 1 262 538 A2 discloses a metal detergent derived from an aromatic carboxylic acid, a metal detergent derived from phenol capable of imparting oxidation resistance in a lubricating oil composition.
  • the aromatic carboxylic acid is a salicylic acid substituted with an alkyl group.
  • composition of the present invention provides detergency and antiwear performance to an oil of lubricating viscosity often used in an engine oil and said composition is substantially free of a metal hydrocarbyl dithiophosphate.
  • the present invention provides a composition comprising:
  • the invention further provides a process for the preparation of a composition comprising mixing:
  • composition of the invention imparts one or more of improved engine cleanliness, decreased wear, decreased NO, emissions and decreased particulate emissions.
  • the present invention provides a composition as described above. Often the composition has a total sulphur content below 0.5 wt %, preferably below 0.3 wt %, more preferably 0.1 wt % and most preferably near 0 wt %. Often the major source of sulphur in the composition of the invention is derived from diluent oil. Usually the diluent oil is used in the manufacturing processes used for preparing many of the component (b) additives.
  • the composition of the invention often have a sulphur content of 700 ppm or less, preferably 600 ppm or less, more preferably 300 ppm or less, even more preferably 100 ppm or less and most preferably 50 ppm or less such as less than 30 ppm, 25 ppm or less, 20 ppm or less and 15 ppm or less.
  • the sulphur content of the composition is often increased by up to 800 ppm, preferably up to 600 ppm and most preferably up to 400 ppm, for instance about 200 ppm or about 300 ppm.
  • the composition has a total phosphorus content below 0.1 wt %, preferably equal to or less than 0.085 wt %, more preferably equal to or less than 0.07 wt %, even more preferably equal to or less than 0.055 wt % and most preferably equal to or less than 0.05 wt % of the composition, such as 200 ppm or less, preferably 100 ppm or less, more preferably 50 ppm or less and most preferably 10 ppm or less.
  • the phosphorus is present from 1 ppm or 10 ppm to 50 ppm or 200 ppm.
  • the composition has a total ash content as determined by ASTM D-874 is below 1.5 wt %, preferably equal to or less than 1.1 wt %, more preferably equal to or less than 1.0 wt %, even more preferably equal to or less than 0.8 wt % and most preferably 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 substrate of the metal salixarate of the invention is often represented by one or a mixture of substantially linear compounds comprising at least one unit of the formulae (I) or (II): 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 is 1, 2 or 3, preferably 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 at
  • 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. Preferably 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, although magnesium, calcium, potassium or mixtures thereof are most preferred.
  • each R 5 can 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 about 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. Pat. No. 6,200,936 and PCT Publications WO 01/56968 and WO 03/18728. It is believed that the salixarate derivatives have a predominantly linear, rather than macrocyclic, structure, although both structures are intended to be encompassed by the term “salixarate.” Additionally “Linear” does not exclude branching or other structures in the substituent R groups.
  • the metal salixarate is often present on an oil free basis at 0.01 to 20, preferably 0.1 to 10, more preferably 0.2 to 8 and most preferably 0.5 to 5 weight percent of the composition.
  • the present invention contains at least one additive selected from the group consisting of (1) an antioxidant; (2) a friction modifier; (3) a dispersant; (4) a viscosity modifier; (5) a dispersant viscosity modifier; and (6) an antiwear agent other than a metal hydrocarbyl dithiophosphate; and
  • the present invention contains at least one additive selected from the group consisting of (1) an antioxidant; (2) a friction modifier; (3) a dispersant; (4) a viscosity modifier; (5) a dispersant viscosity modifier; and (6) an antiwear agent other than a metal hydrocarbyl dithiophosphate. Often 2 or more and most preferably 3 or more of additives (1)-(6) are present in the invention.
  • each of the additives (1)-(6) are present on an oil free basis at 0 to 25, preferably 0.1 to 20, more preferably 0.3 to 15 and most preferably 1 to 10 weight percent of the composition, with the proviso that at least one additive is present at 0.1 or more weight percent of the composition.
  • the antioxidant often includes a diphenylamine antioxidant, a hindered phenol antioxidant, or mixtures thereof.
  • antioxidant additives such as a molybdenum dithiocarboamate or a sulphurised olefin may also be added to the composition of the invention, although preferably the composition is substantially free of a molybdenum dithiocarboamate or a sulphurised olefin.
  • the term “substantially free of a molybdenum dithiocarboamate or a sulphurised olefin” means the composition will contain a molybdenum dithiocarboamate or a sulphurised olefin present at less than 100 ppm, preferably less than 20 ppm and most preferably 1 ppm or less.
  • the diphenylamine suitable for the invention is often represented by the formula: wherein are independently a hydrocarbyl group; and z is zero or higher, provided that on at least one ring, z is non-zero.
  • the hydrocarbyl group contains 1 to 24, preferably 2 to 18 and most preferably 4 to 12 carbon atoms.
  • diphenylamine antioxidants examples include octyl diphenylamine, nonyl diphenylamine, bis-octyl diphenylamine, bis-nonyl diphenylamine or mixtures thereof.
  • the diphenylamine is often present on an oil free basis at 0.01 to 20, preferably 0.05 to 10, more preferably 0.1 to 5 and most preferably 0.2 to 3 weight percent of the composition.
  • the hindered phenol suitable for the invention is often represented by the formula: wherein R 8 and R 9 are independently branched or linear alkyl groups containing 1 to 24, preferably 4 to 18, and most preferably 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 8 and R 9 may be either straight or branched chain; branched is preferred. Suitable examples of R 8 and R 9 include secondary butyl and tertiary butyl.
  • the hindered phenol of formula (VII) suitable for the invention are esters or acids represented by the formula: wherein R 8 and R 9 are as defined above and R 10 is hydrogen, a hydrocarbyl group or mixtures thereof.
  • R 10 is a hydrocarbyl group
  • R 10 is preferably 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 (VII) suitable for the invention contains a bridging group.
  • suitable bridging groups include an alkylene bridge or an ether bridge, often containing 1 to 8, preferably 1 to 6, more preferably 1 to 4 and most preferably 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 11 and R 12 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 8 , E and Y are defined above.
  • suitable methylene-bridged hindered phenol of formula (VIII) include 2,2 -methylene-bis-(4-methyl-6-tert-butylphenol), and 2,2′-methylene-bis-(4-ethyl-6-tert-butylphenol), 2,2′-methylene-bis-(4-propyl-6-tert-butylphenol).
  • the hindered phenol is often present on an oil free basis at 0.01 to 25, preferably 0.1 to 20, more preferably 0.5 to 15 and most preferably 1 to 10 weight percent of the composition.
  • the invention further includes a dispersant often derived from N-substituted long chain alkenyl succinimide or mixtures thereof.
  • the dispersants can be used alone or in combination with other dispersants.
  • 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, preferably 400 to 7000, more preferably 500 to 5000 and most preferably 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 U.S. Pat. Nos. 3,361,673, 3,401,118 and 4,234,435.
  • Mannich bases 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. Pat. No. 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. Pat. No. 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. Pat. No. 4,654,403.
  • the dispersant is often present on an oil free basis at 0.01 to 20, preferably 0.1 to 15, more preferably 0.2 to 10 and most preferably 0.5 to 6 weight percent of the composition.
  • the friction modifier can 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, preferably 10 to 90, more preferably 20 to 85 and most preferably 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; preferably, diethylene glycol, triethylene glycol, glycerol, sorbitol, pentaerythritol and 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 preferred, for instance, 14 to 20 or 16 to 18 carbon atoms. Such acids can be used in combination with acids with more or fewer carbon atoms as well.
  • the acid is a monocarboxylic acid.
  • carboxylic acids include dodecanoic acid, stearic acid, lauric acid, behenic acid, and oleic acid.
  • esters used in the present invention are in particular the monoesters of such polyols and such carboxylic acids.
  • a preferred ester is glycerol monooleate.
  • glycerol monooleate 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 about 60 ⁇ 5 percent by weight of the chemical species “glycerol monooleate,” along with 35 ⁇ 5 percent glycerol dioleate, and less than about 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, sulfurised olefins, fatty imidazolines, condensation products of carboxylic acids and polyalkylene-polyamines, amine salts of alkylphosphoric acids.
  • the friction modifier is free of sulphur and/or phosphorus.
  • the friction modifier is often present on an oil free basis at 0.01 to 20, preferably 0.05 to 10, more preferably 0.1 to 5 and most preferably 0.2 to 3 such as 0.5 to 2 weight percent of the composition.
  • the viscosity modifier is often an olefin copolymer.
  • the olefin copolymer backbone often contains two to four, preferably two to three and most preferably two different olefin monomers.
  • the olefin monomers often contain 2 to 20, preferably 2 to 10, more preferably 2 to 6 and most preferably 2 to 4 carbon atoms.
  • the viscosity modifiers are often present on an oil free basis at of 0.01 to 15, preferably 0.05 to 10, more preferably 0.1 to 5 and most preferably 0.2 to 3 weight percent of the composition.
  • the olefin copolymer preferably contains an ethylene monomer and at least one other comonomer derived from an alpha-olefin having the formula H 2 C ⁇ CHR 10 , wherein R 10 is a hydrocarbyl group, preferably an alkyl radical containing 1 to 18, preferably 1 to 10, more preferably 1 to 6 and most preferably 1 to 3 carbon atoms.
  • R 10 is a hydrocarbyl group, preferably an alkyl radical containing 1 to 18, preferably 1 to 10, more preferably 1 to 6 and most preferably 1 to 3 carbon atoms.
  • the hydrocarbyl group includes an alkyl radical that has a straight chain, a branched chain or mixtures thereof.
  • Suitable comonomers 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.
  • the comonomer is 1-butene, propylene or mixtures thereof.
  • olefin copolymers include ethylene-propylene copolymers or ethylene-butene-1 copolymers.
  • viscosity modifiers suitable for the invention include polymeric materials including hydrogenated styrene-butadiene rubbers, 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.
  • polymeric materials including hydrogenated styrene-butadiene rubbers, 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 copo
  • the olefin copolymer of the invention is 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 additives and their preparation are disclosed, for instance, in U.S. Pat. Nos. 6,107,258 and 6,107,257.
  • olefin copolymer DVM's examples include those commercially available from DSM as PA1250TM, PA1260TM and PA1274TM as well as Hitec 5777TM (commercially available from Ethyl Corporation).
  • the dispersant viscosity modifier is selected from the group consisting of (a) an olefin copolymer grafted with an unsaturated dicarboxylic acid anhydride or derivatives thereof and an amine; (b) a polymethacrylate functionalised with an amine; (c) an esterified copolymer comprising (i) styrene, (ii) an unsaturated dicarboxylic acid anhydride or derivatives thereof, optionally functionalised with an amine; and mixtures thereof.
  • DVM's derived from a polymethacrylate and/or a styrene copolymer are prepared by reacting with an amine as described in U.S. Pat. Nos. 6,107,258 and 6,107,257. The DVM can be used alone or in combination with other DVM's.
  • the dispersant viscosity modifier is often present on an oil free basis at 0.01 to 10, preferably 0.05 to 6, more preferably 0.08 to 4 and most preferably 0.1 to 2 weight percent of the composition.
  • composition of the invention may additionally contain an antiwear agent other than a metal hydrocarbyl dithiophosphate.
  • Suitable antiwear agents include phosphoric acid esters or salt thereof; phosphites; and phosphorus-containing carboxylic esters, ethers, and amides or mixtures thereof.
  • the composition of the invention is substantially free of phosphorus— and/or sulphur-containing antiwear agents. In one embodiment of the invention the composition is free of antiwear agents.
  • the term “substantially free of antiwear agents containing sulphur and/or phosphorus” means the composition will contain antiwear agents present at less than 50 ppm, preferably less than 10 ppm and most preferably 1 ppm or less. In one embodiment of the invention no antiwear agents containing sulphur and/or phosphorus are present. In one embodiment of the invention 1 ppm to 15 ppm of antiwear agents containing sulphur and/or phosphorus are present.
  • 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); alkylated diphenyl ethers and alkylated diphenyl sulphides and the derivatives, analogs and homologs thereof or mixtures thereof.
  • the synthetic lubricating oils are free of alkylated diphenyl sulphides.
  • 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.
  • the synthetic lubricating oils are free of phosphorus-containing esters.
  • 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; preferably an API Group II, III, IV or V oil and mixtures thereof; and most preferably 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 %, preferably up to a maximum of 10 wt %, more preferably up to a maximum of 5 wt % and most preferably 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, YubaseTM 4, YubaseTM 6, and ShellTM XHVI 5.2.
  • the oil of lubricating viscosity is often present at up to 99.98, preferably up to 99.8, more preferably up to 99.65 and most preferably up to 99.3 weight percent of the composition.
  • the present invention is in the form of a concentrate (which can 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.
  • the invention is substantially free of to free of a metal hydrocarbyl dithiophosphate often represented by the formula: wherein R 11 and R 12 are independently hydrogen, hydrocarbyl groups or mixtures thereof, provided that at least one of R 11 and R 12 is a hydrocarbyl group, preferably alkyl or cycloalkyl with 1 to 30, preferably 2 to 20 and most preferably 2 to 15 carbon atoms.
  • the term “substantially free of” means that the composition contains 400 ppm or less of phosphorus, preferably 300 ppm or less of phosphorus, more preferably 200 ppm or less of phosphorus, even more preferably 100 ppm or less of phosphorus and most preferably 100 ppm or less of phosphorus such as 50 ppm, 20 ppm or 1 ppm or less, derived from a metal hydrocarbyl dithiophosphate. In one embodiment of the invention the composition contains 0.5 ppm or 10 ppm to 50 ppm of phosphorus derived from a metal hydrocarbyl dithiophosphate. In one embodiment of the invention the composition is free of a metal hydrocarbyl dithiophosphate.
  • M′ is a metal, and n is an integer equal to the available valence of M′.
  • M′ is mono- or di- or tri-valent, preferably divalent, more preferably 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).
  • composition of the invention optionally further includes other performance additives.
  • the other performance additives selected from the group consisting of detergents other than those of component (a) of the invention, corrosion inhibitors, 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 20, preferably 0.01 to 15, more preferably 0.05 to 10 and most preferably 0.1 to 5 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.
  • Detergents other than those of component (a) of the invention include neutral or overbased, Newtonian or non-Newtonian, basic salts of alkali, alkaline earth and transition metals with one or more of a phenate, a sulphonate, a carboxylic acid, a phosphorus acid, a mono- and/or a di-thiophosphoric acid, a saligenins, an alkylsalicylate or mixtures thereof.
  • Commonly used metals include sodium, potassium, calcium, magnesium lithium or mixtures thereof. Most commonly used metals include sodium, magnesium and calcium.
  • the composition of the invention is free of detergents containing sulphur and/or phosphorus.
  • performance additives such as corrosion inhibitors including 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 (FN 13
  • the invention further provides a process for the preparation of a composition as described above.
  • Components (a)-(c) are often mixed sequentially, separately for the composition of the invention.
  • the mixing conditions are often 15° C. to 130° C., preferably 20° C. to 120° C. and most preferably 25° C. to 110° C.; and for a period of time in the range 30 seconds to 48 hours, preferably 2 minutes to 24 hours, more preferably 5 minutes to 16 hours and most preferably 10 minutes to 5 hours; and at pressures in the range 86 kPa to 266 kPa (650 mm Hg to 2000 mm Hg), preferably 91 kPa to 200 kPa (690 mm Hg to 1500 mm Hg), and most preferably 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 in an 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 one or more of the group selected from improved engine cleanliness, decreased wear, decreased NO x emissions and decreased particulate emissions.
  • a sample of a salixarene substrate is prepared using a flange flask approximately 2 litres in volume, a flange and clip, overhead stirrer with paddle and polytetrafluoroethylene (PTFE) stirrer gland, Dean Stark trap and double surface condenser, an electric mantle/thermocouple/EurothermTM temperature controller system, the glassware from just above the mantle to just below the condenser being covered with glass wool.
  • PTFE polytetrafluoroethylene
  • the flask is filled with 475 g polyisobutenyl phenol derived from high vinylidene polyisobutylene with a number average molecular weight of 550 (GLISSOPAL®550 commercially available from BASF) and 330 g of mineral oil (SN 150) and heated to 30° C. via a pressure equalizing dropping funnel 3.4 g of 50% aqueous KOH is added.
  • the contents of the flask are heated to 75° C. and the temperature is kept constant for 30 minutes while 81.6 g of 37% aqueous formaldehyde (formalin) is added.
  • the reaction is charged with 51.6 g of salicylic acid and heated to 140° C. while controlling reflux. Water is removed using Dean Stark trap.
  • the product is vacuum stripped at 140° C./13 kPa (equivalent to 100 mm Hg) for 30 minutes.
  • a more detailed description of the reaction process is given in Examples 1 and 5 of International Publication WO03/018728, pages 22 and 23
  • a vessel is charged with 1200 g of the salixarene from Preparative Example 1, 25 g of ethylene glycol, 130 g of calcium hydroxide and 410 g of 2-ethylhexanol.
  • the vessel and contents are heated to 95° C. and stirred under vacuum (64 kPa, which is equivalent to 480 mm Hg).
  • the vessel and contents are then subject to vacuum at 6.7 kPa (equivalent to 50 mm Hg) for 15 minutes and heated to 130° C..
  • the vessel is then charged with an additional 120 g of ethylene glycol added dropwise over 10 minutes before carbon dioxide is added via a dip tube under a slight negative pressure at 1.0 g/minute or less until 48g are added.
  • the dip tube Upon completion of carbon dioxide addition, the dip tube is removed and the temperature is increased to 200° C. under a vacuum of 6.7 kPa (equivalent to 50 mm Hg) to remove solvents. The residue is vacuum filtered through a 12 mm diatomaceous earth pad in a sintered funnel yielding a viscous brown liquid.
  • a vessel is charged with 560.5 g of the salixarene from Preparative Example 1 with 433 g of xylene.
  • the vessel and contents are heated to 35° C. under a nitrogen atmosphere where 53 g of magnesium oxide is added.
  • the vessel is then charged with 20.2 g of glacial acetic acid and then a mixture of methanol (42 g) and water (30 g) is added.
  • the vessel and contents are heated to 61° C. and carbonated.
  • the vessel and contents are held at 61° C. for a further 2 hours and a further mixture of methanol (36 g) and water (26.2 g) is added.
  • the vessel heated to 150° C. and held for 1 hour.
  • the product is vacuum stripped.
  • a vessel is charged with 313 g of the salixarene from Preparative Example 1, and heated under a nitrogen atmosphere to 80° C. where 12.1 g of potassium hydroxide in 7 g of water is added dropwise followed by the addition of 85 g of a diluent oil.
  • the vessel and contents are heated to 110° C. for 10 minutes, then heated to 120° C. for 90 minutes and heated to 140° C. for 3 hours. A dark brown product is formed.
  • a composition is prepared by mixing (a) 42.5 g of NexbaseTM3050 oil, (b) 34.4 g of NexbaseTM3043 oil, (c) on a an oil free basis 0.4 g of an amine dispersant viscosity modifier, (d) on a an oil free basis 2.8 g of polyisobutylene succinimide dispersants, (e) 5 g of antioxidants including a diphenylamine and a hindered phenol, (f) 0.7 g of an olefin copolymer viscosity modifier and (g) a glycerol monooleate friction modifier.
  • the composition contains 0 wt % of calcium, 0 wt % of phosphorus, 190 ppm of sulphur and 0 wt % of zinc.
  • the composition has a KV100 of 13.11 mm 2 /s (cSt) and a sulphated ash content of 0 wt %.
  • Reference Example 2 is a successful European top tier passenger car oil formulation containing zinc dithiophosphate.
  • the elemental analysis of the oil formulation indicates a calcium content of 3307 ppm, a phosphorus content of 889 ppm, a sulphur content of 2645 ppm and a zinc content of 889 ppm.
  • the oil formulation has a KV100 of 11.3 mm 2 /s (cSt) and sulphated ash content of 1.26 wt %.
  • Example 1 has the same composition as Reference Example 1 except 2.5 g (on an oil free basis) of the product of Preparative Example 2 is also added.
  • the phosphorus content is 0 wt % and the sulphur content is 190 ppm (all derived from diluent oil).
  • Example 2 has the same composition as Reference Example 1 except 2.5 g (on an oil free basis) of the product of Preparative Example 3 is also added.
  • the phosphorus content is 0 wt % and the sulphur content is 190 ppm (all derived from diluent oil).
  • Example 3 has the same composition as Reference Example 1 except 2.5 g (on an oil free basis) of the product of Preparative Example 4 is also added.
  • the phosphorus content is 0 wt % and the sulphur content is 190 ppm (all derived from diluent oil).
  • a number of lubricating oil compositions are formed using Reference Example 1 and adding examples 1-3 at 2.5 g on a oil free basis to the oil thus forming “Lubricating Oil Composition with Example 1”, Example 2 is titled “Lubricating Oil Composition with Example 2” and “Lubricating Oil Composition with Example 3.”
  • Reference example 1 and the corresponding Lubricating Oil Composition with examples 1-3 have a KV100 of 13.11 mm 2 /s (or cSt).
  • Test 1 HFRR of Examples 1-3 and Reference Examples 1-2
  • Lubricating Oil Composition with Example 1-3 are and Reference Example 1-2 are evaluated for wear performance in a programmed temperature high frequency reciprocating rig (HFRR) available from PCS Instruments.
  • HFRR conditions for the evaluations are 200 g load, 75 minute duration, 1000 micrometer stroke, 20 hertz frequency, and temperature profile of 15 minutes at 40° C. followed by an increase in temperature to 160° C. at a rate of 2° C. per minute. Wear scar in micrometers and film formation as percent film thickness are measured with lower wear scar values and higher film formation values indicating improved wear performance.
  • the percent film thickness is based on the measurement of electrical potential between an upper and a lower metal test plate in the HFRR.
  • the film thickness is 100%, there is a high electrical potential for the full length of the 1000 micrometre stroke, suggesting no metal to metal contact.
  • a film thickness of 0% there is no electrical potential suggesting continual metal to metal contact between the plates.
  • the upper and lower metal test plate have a degree of metal to metal contact as well as other areas with no metal to metal contact.
  • the Cameron Plint TE-77TM is a reciprocating wear tester. In this test a steel ball upper specimen is reciprocated against a steel flat lower specimen. The Cameron Plint is charged with 10 ml of sample and heated to 50° C. and held for 1 minute. The sample is then subject to a load of 100N over two minutes while at the same time the reciprocation is started at 10 Hz over 15mm stroke length. The sample is then heated to 250° C. at 3° C. per minute. At the end of-the test the average diameter of the wear scar (in micrometers) on the ball (measured in the X and Y directions) is measured using a calibrated microscope. The results obtained are: TABLE 2 Cameron Plint Wear Scar Data Example Wear Scar Lubricating Oil Composition Example 1 396 Reference Example 1 753 Reference Example 2 517 Test 3: 4 Ball Wear Test Using ASTM D4172
  • Example 4 contains 2 g on a oil free basis of the product of Preparative Example 2 and delivering about 1900 ppm of calcium and a TBN of about 146; and “Example 5” contains 1.2 g on a oil free basis of the product of preparative Example 2 and delivering about 1300 ppm of calcium and a TBN of about 146.
  • Reference Example 3 has the same oil composition as Reference Example 1, except a calcium alkylsalicylate (commercially available from AC60CTM range of products from Infineum) is added in sufficient quantity to deliver about 1300 ppm of calcium and a TBN of about 146.
  • Reference Example 4 has the same oil composition as Reference Example 1, except a magnesium saligenin (commercially available from The Lubrizol Corporation) is added in sufficient quantity to deliver about 1300 ppm of magnesium and a TBN of about 146.
  • 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 is attached to the remainder of the molecule through a carbon atom and 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, preferably 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 described in U.S. Pat. No. 6, 583,092.

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US20070298987A1 (en) * 2006-06-23 2007-12-27 Marc-Andre Poirier Lubricating compositions
US20090061234A1 (en) * 2007-09-04 2009-03-05 Baker Hughes Incorporated Method for Inhibiting Corrosion of Metal in Distillation Units Caused by Organic Acids
US20090156446A1 (en) * 2004-10-25 2009-06-18 Mcatee Rodney J Corrosion Inhibition
US20100210493A1 (en) * 2009-02-18 2010-08-19 Chevron Oronite Company Llc Lubricating oil compositions

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JP2011214013A (ja) 2011-10-27
JP2007517937A (ja) 2007-07-05

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