EP3851508B1 - Procédé de lubrification d'un moteur à combustion interne - Google Patents

Procédé de lubrification d'un moteur à combustion interne Download PDF

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Publication number
EP3851508B1
EP3851508B1 EP21150240.6A EP21150240A EP3851508B1 EP 3851508 B1 EP3851508 B1 EP 3851508B1 EP 21150240 A EP21150240 A EP 21150240A EP 3851508 B1 EP3851508 B1 EP 3851508B1
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EP
European Patent Office
Prior art keywords
molecular weight
group
derived
metal
lubricating
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EP21150240.6A
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German (de)
English (en)
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EP3851508A1 (fr
Inventor
John G. Loop
Mary Galic Raguz
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Lubrizol Corp
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Lubrizol Corp
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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
    • 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
    • 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
    • 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
    • C10M159/18—Complexes with metals
    • C—CHEMISTRY; METALLURGY
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    • 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
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    • 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
    • C10M159/24—Reaction mixtures having an excess of neutralising base, e.g. so-called overbasic or highly basic products containing sulfonic radicals
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    • C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/102—Aliphatic fractions
    • C10M2203/1025—Aliphatic fractions used as base material
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    • C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
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    • C10M2205/0285—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms used as base material
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    • 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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    • C10N2040/25—Internal-combustion engines
    • C10N2040/255—Gasoline engines
    • C10N2040/26—Two-strokes or two-cycle engines

Definitions

  • the disclosed technology relates to lubricants, particularly for internal combustion engines including diesel engines.
  • the disclosed technology relates to lower viscosity lubricating compositions which provide improved protection against adhesive wear.
  • Adhesive wear occurs when material from two mated metal parts is transferred unevenly from one part to the other due to a lubricant's inability to maintain separation of the two parts or inability to maintain a low enough temperature in the system. In these cases, the mated parts develp micro-welds which are then torn away as the two parts move away from each other. Adhesive wear is often addressed by increasing the viscosisty of the lubricant and/or by increasing the amount of anti-wear addtives in the lubricating composition.
  • Certain lubricating compositions such as crankcase lubricants, are being formulated with lower high temperature high shear (HTHS) viscosities in order to improve fuel economy.
  • some lubricating compositions are being formulated with lower levels of anti-wear additives, in particular, phosphorous or sulfur containing anti-wear additives, for environmental reasons.
  • the reduction in HTHS viscosity and/or anti-wear additives generally causes an increase in adhesive wear on the metal to metal surfaces.
  • WO2016/070002 A1 discloses a lubricating composition
  • a lubricating composition comprising: an oil of lubricating viscosity, an alkali earth metal sulphonate detergent present in an amount to provide at least 1 wt % sulphonate soap to the lubricating composition, an alkaline earth metal phenol-based detergent present in amount to provide at least 3.5 wt % phenol-containing soap to the lubricating composition, wherein the sulphonate detergent provides no more than 50% of the total base number derived from a detergent, and the lubricating composition has a total base number of 10 to 25 mg KOH/g (as measured by ASTM D2986-11).
  • the present invention is directed to a method of reducing adhesive wear in a compression engine lubricated with a low phosphorus lubricant composition comprising less than 0.1 wt % phosphorous and having a viscosity of 10 centistokes or lower at 100°C measured in accordance with to ASTM D445-17, comprising supplying to the engine a lubricant composition comprising an oil of lubricating viscosity, one or more metal-containing sulfur-free detergents derived from an alkylphenol in an amount to deliver at least 0.2 weight percent alkylphenol-containing soap to the composition, one or more alkaline earth metal sulfonate detergents in an amount to deliver at least 0.8% by weight sulfonate soap to the composition, 1 wt % to 4.5 wt % of one or more polyisobutenyl succinimide dispersants, and 0.1 wt % to 1.2 wt % of a dispersant viscosity modifier derived from a
  • the disclosed technology provides a lubricating composition and a method for lubricating an internal combustion engine.
  • the lubricating composition comprises an oil of lubricating viscosity, one or more metal-containing sulfur-free detergents derived from an alkylphenol in an amount to deliver at least 0.2 weight percent alkylphenol-containing soap to the composition, 1 wt % to 4.5 wt % of one or more polyisobutenyl succinimide dispersants, one or more alkaline earth metal sulfonate detergents in an amount to deliver at least 0.8% by weight sulfonate soap to the composition, and 0.1 wt % to 1.2 wt % of a dispersant viscosity modifier derived from a polyolefin having a number average molecular weight of at least 20,000, wherein the lubricant composition contains less than 0.2 wt % of a sulfur-coupled phenate detergent.
  • the lubricating composition comprises an oil of lubricating viscosity.
  • oils include natural and synthetic oils, oil derived from hydrocracking, hydrogenation, and hydrofinishing, unrefined, refined and re-refined oils and mixtures thereof.
  • the varoius types of oils of lubricating viscosity are desribed herein below and may be used in the lubricating composition of the present invention.
  • 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,), 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,
  • 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 dodecylbenzenes, tetradecylbenzenes, dinonylbenzenes, di-(2-ethylhexyl)-benzenes); polyphenyls (e.g., biphenyls, terphenyls, alkylated polyphenyls); diphenyl alkanes, alkylated diphenyl alkanes, alkylated diphenyl ethers and alkylated diphenyl sulfides and the derivatives, analogs and homologs thereof or mixtures thereof.
  • polyphenyls e.g., biphenyls, terphenyls, alkylated polyphenyls
  • diphenyl alkanes alkylated diphenyl alkanes, alkylated diphenyl ethers and alkylated diphenyl sulfides and the derivatives, analogs and homologs thereof or mixture
  • synthetic lubricating oils include polyol esters (such as Priolube ® 3970), diesters, liquid esters of phosphorus-containing acids (e.g., tricresyl phosphate, trioctyl phosphate, and the diethyl ester of decane phosphonic acid), or polymeric tetrahydrofurans.
  • Synthetic oils may be produced by Fischer-Tropsch reactions and typically may be hydroisomerised Fischer-Tropsch hydrocarbons or waxes. In one embodiment oils may be prepared by a Fischer-Tropsch gas-to-liquid synthetic procedure as well as other gas-to-liquid oils.
  • 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 (sulfur content >0.03 wt %, and/or ⁇ 90 wt % saturates, viscosity index 80-120); Group II (sulfur content ⁇ 0.03 wt %, and ⁇ 90 wt % saturates, viscosity index 80-120); Group III (sulfur content ⁇ 0.03 wt %, and ⁇ 90 wt % saturates, viscosity index ⁇ 120); Group IV (all polyalphaolefins (PAOs)); and Group V (all others not included in Groups I, II, III, or IV).
  • PAOs polyalphaolefins
  • the oil of lubricating viscosity may also be an API Group 11+ base oil, which term refers to a Group II base oil having a viscosity index greater than or equal to 110 and less than 120, as described in SAE publication " Design Practice: Passenger Car Automatic Transmissions", fourth Edition, AE-29, 2012, page 12-9 , as well as in US 8,216,448 , column 1 line 57.
  • API Group 11+ base oil refers to a Group II base oil having a viscosity index greater than or equal to 110 and less than 120, as described in SAE publication " Design Practice: Passenger Car Automatic Transmissions", fourth Edition, AE-29, 2012, page 12-9 , as well as in US 8,216,448 , column 1 line 57.
  • the oil of lubricating viscosity may also be an API Group III+ base oil, which term refers to a Group III+ base oil having a viscosity index greater than or equal to 130.
  • Group III+ are known in the art and is described in " Lube Report", dated February 26, 2014 in an article entitled “SK Sees Group III Shortfall", by Nancy DeMarco. The article may be obtained from http://www.aselube.com/media/11910/sk sees group iii shortfall.pdf .
  • the oil of lubricating viscosity may be an API Group IV oil, or mixtures thereof, i.e., a polyalphaolefin.
  • the polyalphaolefin may be prepared by metallocene catalyzed processes or from a non-metallocene process.
  • the oil of lubricating viscosity may comprise an API Group I, or Group II, or Group III, or Group IV, or Group V oil, or mixtures thereof.
  • the amount of the oil of lubricating viscosity present may be typically the balance remaining after subtracting from 100 wt % the sum of the amount of the additive as described herein above, and the other performance additives.
  • the lubricating composition may be in the form of a concentrate and/or a fully formulated lubricant. If the lubricating composition of the disclosed technology 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 the of components of the disclosed technology to the oil of lubricating viscosity and/or to diluent oil include the ranges of 1:99 to 99:1 by weight, or 80:20 to 10:90 by weight.
  • the lubricating composition may be a non-aqueous composition.
  • the oil of lubricating viscosity may refer to a single base oil or a mixture of base oils.
  • the oil of lubricating viscosity used in the lubricating composition of the present invention may have a kinematic viscosity of 2 cSt to 20 cSt (or mm 2 /s) at 100°C, as measured by ASTM D445-14.
  • the lubricating composition may be liquid, i.e., not a gel or semi-solid, at ambient temperatures (5-30°C).
  • the lubricating composition contains a metal containing sulfur-free detergent and an alkaline earth metal containing sulfonate detergent.
  • the lubricating composition may contain small amounts of sulfur-coupled phenate detergents.
  • the term "soap” means the surfactant portion of a detergent and does not include a metal base, such as calcium carbonate.
  • a metal base such as calcium carbonate.
  • the "soap content”, metal ratio and TBN are known to a person skilled in the art and explained in standard textbook entitled “ Chemistry and Technology of Lubricants", Third Edition, Edited by R. M. Mortier and S. T. Orszulik, Copyright 2010, pages 219 to 220 under the sub-heading 7.2.5. Detergent Classification.
  • the term “soap” may also be referred to as a detergent substrate.
  • the sulfonate detergents described herein, the soap may be a neutral salt of an alkylbenzenesulfonic acid.
  • Overbased metal detergents are often referred to as "overbased metal detergents.” Overbased metal detergents may be viewed as comprising an oil-soluble neutral metal salt component and a metal carbonate component. Overbased materials, otherwise referred to as overbased or superbased salts, are generally homogeneous Newtonian systems characterized by a metal content in excess of that which would be present for neutralization according to the stoichiometry of the metal and the particular acidic organic compound reacted with the metal.
  • the overbased materials are prepared by reacting an acidic material (typically an inorganic acid or lower carboxylic acid, in one embodiment carbon dioxide) with a mixture comprising an acidic organic compound, a reaction medium comprising at least one inert, organic solvent (e.g., mineral oil, naphtha, toluene, xylene) for the acidic organic material, a stoichiometric excess of a metal base, and a promoter such as a phenol or alcohol and optionally ammonia.
  • the acidic organic material will normally have a sufficient number of carbon atoms, for instance, as a hydrocarbyl substituent, to provide a reasonable degree of solubility in oil.
  • the amount of excess metal is commonly expressed in terms of metal ratio.
  • metal ratio is the ratio of the total equivalents of the metal to the equivalents of the acidic organic compound.
  • a neutral metal salt has a metal ratio of one.
  • a salt having 4.5 times as much metal as present in a normal salt will have metal excess of 3.5 equivalents, or a ratio of 4.5.
  • TBN Total Base Number
  • TBN is the amount of strong acid needed to neutralize all of the overbased material's basicity, expressed as potassium hydroxide equivalents (mg KOH per gram of sample). Since overbased detergents are commonly provided in a form which contains a certain amount of diluent oil, for example, 40-50% oil, the actual TBN value for such a detergent will depend on the amount of such diluent oil present, irrespective of the "inherent" basicity of the overbased material. For the purposes of the present invention, the TBN of an overbased detergent is to be recalculated to an oil-free basis.
  • Detergents which are useful in the lubricating composition of the present invention may have a TBN (oil-free basis) of 100 to 800, and in one embodiment 150 to 750, and in another, 400 to 700. If multiple detergents are employed, the overall TBN of the detergent component (that is, an average of all the specific detergents together) will typically be in the above ranges.
  • the metal compounds useful in making the basic metal salts are generally any Group 1 or Group 2 metal compounds (CAS version of the Periodic Table of the Elements).
  • the Group 1 metals of the metal compound include Group la alkali metals such as sodium, potassium, and lithium, as well as Group 1b metals such as copper.
  • the Group 1 metals can be sodium, potassium, lithium and copper, and in one embodiment sodium or potassium, and in another embodiment, sodium.
  • the Group 2 metals of the metal base include the Group 2a alkaline earth metals such as magnesium, calcium, and barium, as well as the Group 2b metals such as zinc or cadmium.
  • the Group 2 metals are magnesium, calcium, barium, or zinc, and in another embodiments magnesium or calcium.
  • the metal is calcium or sodium or a mixture of calcium and sodium.
  • the anionic portion of the salt can be hydroxide, oxide, carbonate, borate, or nitrate.
  • the lubricating composition comprises an overbased detergent.
  • the lubricating composition comprises one or more deterents dervived from an alkylphenol.
  • the metal containing dergent derived from an alkylphenol is sulfur-free.
  • the metal-containing detergent derived from an alkylphenol may be an overbased phenate detergent.
  • the phenols useful in making phenate detergents can be represented by the formula (R 1 ) a -Ar-(OH) b , wherein R 1 is an aliphatic hydrocarbyl group of 4 to 400 carbon atoms, or 6 to 80 or 6 to 30 or 8 to 25 or 8 to 15 carbon atoms; Ar is an aromatic group (which can be a benzene group or another aromatic group such as naphthalene); a and b are independently numbers of at least one, the sum of a and b being in the range of two up to the number of displaceable hydrogens on the aromatic nucleus or nuclei of Ar.
  • a and b are independently numbers in the range of 1 to 4, or 1 to 2.
  • R 1 and a are typically such that there are an average of at least 8 aliphatic carbon atoms provided by the R 1 groups for each phenol compound.
  • Phenate detergents are also sometimes provided as sulfur-bridged species.
  • the lubricating composition may comprise at least one sulfur-free phenate detergent.
  • the lubricating composition contains less than 0.2 wt %, or even less than 0.15 wt %. of a sulfur-coupled phenate detergent.
  • the lubricating composition is substantially free of sulfur-coupled phenate detergents.
  • the lubricating composition is free of sulfur-coupled phenate detergents.
  • the overbased alkyl-phenol based detergent may be an overbased saligenin detergent.
  • Overbased saligenin detergents are commonly overbased magnesium salts which are based on saligenin derivatives.
  • a general example of such a saligenin derivative can be represented by Formula (1): wherein X comprises -CHO or -CH 2 OH, Y comprises -CH 2 - or -CH 2 OCH 2 -, and wherein such -CHO groups typically comprise at least 10 mole percent of the X and Y groups;
  • M is hydrogen, ammonium, or a valence of a metal ion (that is to say, in the case of a multivalent metal ion, one of the valences is satisfied by the illustrated structure and other valences are satisfied by other species such as anions, or by another instance of the same structure)
  • R 1 is a hydrocarbyl group containing 1 to 60 carbon atoms
  • m is 0 to typically 10
  • each is independently 0, 1, 2, or 3, provided that at least
  • one of the X groups can be hydrogen.
  • M is a valence of a Mg ion or a mixture of Mg and hydrogen.
  • Saligenin detergents are disclosed in greater detail in U.S. Patent 6,310,009 , with special reference to their methods of synthesis (Column 8 and Example 1) and preferred amounts of the various species of X and Y (Column 6).
  • the overbased alkyl-phenol based detergent may also comprise salixarate detergents.
  • Salixarate detergents are overbased materials that can be represented by a substantially linear compound comprising at least one unit of formula (2) or formula (3): each end of the compound having a terminal group of formula (4) or (5): such groups being linked by divalent bridging groups A, which may be the same or different for each linkage; wherein in formulas (2)-(5) R 3 is hydrogen or a hydrocarbyl group or a valence of a metal ion; R 2 is hydroxyl or a hydrocarbyl group and j is 0, 1, or 2; R 6 is hydrogen, a hydrocarbyl group, or a hetero-substituted hydrocarbyl group; either R 4 is hydroxyl and R 5 and R 7 are independently either hydrogen, a hydrocarbyl group, or hetero-substituted hydrocarbyl group, or else R 5 and R 7 are both hydroxyl and R 4 is hydrogen, a hydrocarbyl group, or
  • Salixarate derivatives and methods of their preparation are described in greater detail in U.S. patent number 6,200,936 and PCT Publication WO 01/56968 . 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.”
  • the alkyl-phenol based overbased detergent used in the lubricating composition also be an overbased salicylate which may be an alkali metal salt or an alkaline earth metal salt of a substituted salicylic acid.
  • the salicylic acids may be hydrocarbyl-substituted salicylic acids wherein each substituent contains an average of at least 8 carbon atoms per substituent and 1 to 3 substituents per molecule.
  • the substituents can be polyalkene substituents, where polyalkenes include homopolymers and interpolymers of polymerizable olefin monomers of 2 to 16, or 2 to 6, or 2 to 4 carbon atoms.
  • the olefins may be monoolefins such as ethylene, propylene, 1-butene, isobutene, and 1-octene; or a polyolefinic monomer, such as diolefinic monomer, such 1,3-butadiene and isoprene.
  • the hydrocarbyl substituent group or groups on the salicylic acid contains 7 to 300 carbon atoms and can be an alkyl group having a molecular weight of 150 to 2000.
  • the polyalkenes and polyalkyl groups are prepared by conventional procedures, and substitution of such groups onto salicylic acid can be effected by known methods.
  • Alkyl salicylates may be prepared from an alkylphenol by Kolbe-Schmitt reaction; alternatively, calcium salicylate can be produced by direct neutralization of alkylphenol and subsequent carbonation.
  • Overbased salicylate detergents and their methods of preparation are disclosed in U.S. Patents 4,719,023 and 3,372,116 .
  • the lubricating composition also comprises an overbased sulfonate detergent.
  • the overbased sulfonate detergent comprieses an alkaline-earth metal containing sulfonate detergent.
  • Sulfonate detergents are derived from sulfonic acids. Suitable sulfonic acids include sulfonic and thiosulfonic acids. Sulfonic acids include the mono- or polynuclear aromatic or cycloaliphatic compounds.
  • Oil-soluble sulfonates can be represented for the most part by one of the following formulas: R 2 -T-(SO 3 -)a and R 3 -(SO 3 -)b, where T is a cyclic nucleus such as typically benzene; R 2 is an aliphatic group such as alkyl, alkenyl, alkoxy, or alkoxyalkyl; (R 2 )-T typically contains a total of at least 15 carbon atoms; and R 3 is an aliphatic hydrocarbyl group typically containing at least 15 carbon atoms. Examples of R 3 are alkyl, alkenyl, alkoxyalkyl, and carboalkoxyalkyl groups.
  • the groups T, R 2 , and R 3 can also contain other inorganic or organic substituents.
  • a and b are at least 1.
  • the sulfonate detergent may be a predominantly linear alkylbenzenesulfonate detergent having a metal ratio of at least 8 as described in paragraphs [0026] to [0037] of US Patent Application 2005065045 .
  • the linear alkyl group may be attached to the benzene ring anywhere along the linear chain of the alkyl group, but often in the 2, 3 or 4 position of the linear chain, and in some instances predominantly in the 2 position.
  • the lubricating composition comprises a sulfonate detergent, such as a magnesium, sodium or zinc overbased sulfonate.
  • a sulfonate detergent such as a magnesium, sodium or zinc overbased sulfonate.
  • any additional sulfonate detergent may be a magnesium or sodium sulfonate detergent, with magnesium sulfonate the more typical.
  • the lubricating composition comprises a 300 TBN or higher alkaline earth metal sulfonate detergent having a metal ratio of 10 to 40, and a 82 to 100 TBN or lower alkaline earth metal sulfonate detergent having a metal ratio of 3 to 9.
  • the lubricating composition comprises a 300 TBN or higher alkaline earth metal sulfonate detergent, which comprises a magnesium sulfonate detergent having a metal ratio of 10 to 40, and a 80 TBN or lower alkaline earth metal sulfonate detergent, which comprises a calcium sulfonate detergent having a metal ratio of 1 to 5.
  • the lubricating composition comprises a 300 TBN or higher alkaline earth metal sulfonate detergent, which comprises a mixture of a calcium sulfonate detergent having a metal ratio of 10 to 40 and a magnesium sulfonate detergent having a metal ratio of 10 to 40, and a 80 TBN or lower alkaline earth metal sulfonate detergent, which comprises a calcium sulfonate detergent having a metal ratio of 1 to 5.
  • the 300 TBN or higher alkaline earth metal sulfonate detergent and the 80 TBN or lower alkaline earth metal sulfonate detergent may be prepared from the same or different hydrocarbyl-substituted sulfonic acids.
  • the hydrocarbyl-substituted sulfonic acids are alkyl-substituted sulfonic acids.
  • the sulfonate may be prepared from a mono- or di- hydrocarbyl-substituted benzene (or toluene, naphthalene, indenyl, indanyl, or bicyclopentadienyl) sulfonic acid, wherein the hydrocarbyl group may contain 6 to 40, or 8 to 35 or 9 to 30 carbon atoms.
  • the hydrocarbyl group may be derived from polypropylene or a linear or branched alkyl group containing at least 10 carbon atoms.
  • a suitable alkyl group include branched and/or linear decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, octadecenyl, nonodecyl, eicosyl, un-eicosyl, do-eicosyl, tri-eicosyl, tetra-eicosyl, penta-eicosyl, hexa-eicosyl or mixtures thereof.
  • the hydrocarbyl-substituted sulfonic acid may include polypropene benzenesulfonic acid and C 16 -C 24 alkyl benzenesulfonic acid, or mixtures thereof.
  • the 300 TBN sulfonate detergent may be a predominantly linear alkylbenzene sulfonate detergent having a metal ratio of having a metal ratio of 10 to 40 as is described in paragraphs [0026] to [0037] of US Patent Application 2005065045 (and granted as US 7,407,919 ).
  • the predominantly linear alkylbenzene sulfonate detergent may be particularly useful for assisting in improving fuel economy.
  • the 300 TBN or higher alkaline earth metal sulfonate detergent has a metal ratio of 12 to 30, or 12 to 22, or 16 to 20, or 10 to 20, or 20 to 30, or 22 to 25. In one embodiment the 300 TBN metal ratio may be 16 to 20, and in another embodiment 22 to 25.
  • the lubricating composition comprises a calcium sulfonate detergent having a metal ratio of 10 to 40, and a calcium sulfonate detergent having a metal ratio of 3 to 9.
  • the lubricating composition comprises a calcium sulfonate detergent having a metal ratio of 10 to 40, a calcium sulfonate detergent having a metal ratio of 3 to 9, and a magnesium sulfonate detergent having a metal ratio of 12 to 40.
  • the magnesium sulfonate detergent may have a TBN of 300 to 800, or 450 to 700 mg KOH/g; and a metal ratio of 12 to 40, or 14 to 25.
  • the magnesium sulfonate may have the same or different hydrocarbyl-substituted sulfonic acids, and are defined the same as described above for calcium sulfonate detergents.
  • overbased detergents can include overbased detergents having a Mannich base structure, as disclosed in U.S. Patent 6,569,818 .
  • Patents describing techniques for making basic salts of sulfonic acids, carboxylic acids, (hydrocarbyl-substituted) phenols, phosphonic acids, and mixtures of any two or more of these include U.S. Patents 2,501,731 ; 2,616,905 ; 2,616,911 ; 2,616,925 ; 2,777,874 ; 3,256,186 ; 3,384,585 ; 3,365,396 ; 3,320,162 ; 3,318,809 ; 3,488,284 ; and 3,629,109 .
  • the lubricating composition of the present invention comprsies one or more metal-containing sulfur-free detergents derived from alkyl-phenol, as described above, in an amount sufficient to deliver at least 0.2 weight percent alkylphenol-containing soap to the composition.
  • the metal-containing sulfur-free detergent may be selected from phenate detergents, alkylsalicylate deteregents, Mg saligenin, or Ca salixarate.
  • the lubricating composition of the present invention also comprises one or more sulfonate detergents in an amount to deliver at least 0.8 weight percent sulfonate soap to the composition.
  • the sulfonate detergent is an alkaline earth metal sulfuonate detergent.
  • the lubricating composition further comprises a succinimide dispersant.
  • the lubricating composition comprises 1 wt % to 4.5 wt % or 1 wt % to 4 wt % polyisobutylene succinimide dispersant.
  • Succinimide dispersants may be derived from polyisobutylene succinimide, wherein the polyisobutylene from which polyisobutylene succinimide may be derived has a number average molecular weight of 350 to 5000, or 750 to 3000 or 1550 to 2500.
  • the dispersant is prepared by a process that involves the presence of small amounts of chlorine or other halogen, as described in U.S. Patent 7,615,521 (see, e.g., col. 4, lines 18-60 and preparative example A). Such dispersants typically have some carbocyclic structures in the attachment of the hydrocarbyl substituent to the acidic or amidic "head” group.
  • the dispersant is prepared by a thermal process involving an "ene” reaction, without the use of any chlorine or other halogen, as described in U.S. Patent 7,615,521 ; dispersants made in this manner are often derived from high vinylidene (i.e. greater than 50% terminal vinylidene) polyisobutylene(See col.
  • dispersants typically do not contain the above-described carbocyclic structures at the point of attachment.
  • the dispersant is prepared by free radical catalyzed polymerization of high-vinylidene polyisobutylene with an ethylenically unsaturated acylating agent, as described in United States Patent 8,067,347 .
  • Dispersants may be derived from, as the polyolefin, high vinylidene polyisobutylene, that is, having greater than 50, 70, or 75% terminal vinylidene groups ( ⁇ and ⁇ isomers).
  • the succinimide dispersant may be prepared by the direct alkylation route. In other embodiments it may comprise a mixture of direct alkylation and chlorine-route dispersants.
  • Suitable dispersants for use in the compositions include succinimide dispersants.
  • the dispersant may be present as a single dispersant.
  • the dispersant may be present as a mixture of two or three different dispersants, wherein at least one may be a succinimide dispersant.
  • the dispersant may also be post-treated by conventional methods by a reaction with any of a variety of agents.
  • agents include boron compounds, urea, thiourea, dimercaptothiadiazoles, carbon disulfide, aldehydes, ketones, carboxylic acids, hydrocarbon-substituted succinic anhydrides, maleic anhydride, nitriles, epoxides, and phosphorus compounds.
  • the dispersant of polyisobutylene succinimide may be derived from an aliphatic polyamine, or mixtures thereof.
  • the lubricating composition comprises a non-borated succinimide dispersant.
  • the aliphatic polyamine may be aliphatic polyamine such as an ethylenepolyamine, a propylenepolyamine, a butylenepolyamine, or mixtures thereof. In one embodiment the aliphatic polyamine may be ethylenepolyamine. In one embodiment the aliphatic polyamine may be chosen from ethylenediamine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine, pentaethylenehexamine, polyamine still bottoms, and mixtures thereof.
  • Polyisobutylene succinimide dispersants and their preparation are disclosed, for instance in US Patents 3,172,892 , 3,219,666 , 3,316,177 , 3,340,281 , 3,351,552 , 3,381,022 , 3,433,744 , 3,444,170 , 3,467,668 , 3,501,405 , 3,542,680 , 3,576,743 , 3,632,511 , 4,234,435 , Re 26,433 , and 6,165,235 , 7,238,650 and EP Patent Application 0 355 895 A .
  • the polyisobutylene succinimide may have a carbonyl to nitrogen ratio of 1:1 to 1:5, or 1:1 to 1:4, or 1:1.3 to 3: or 1:1.5 to 1:2, or 1:1.4 to 1:0.6.
  • the polyisobutylene succinimide dispersant may include an amine-functionalized additive may be derived from an amine having at least 3 or 4 aromatic groups.
  • an aromatic group is used in the ordinary sense of the term and is known to be defined by Hückel theory of 4n+2 ⁇ electrons per ring system. Accordingly, one aromatic group may have 6, or 10, or 14 ⁇ electrons. Hence a benzene ring has 6 ⁇ electrons, a naphthylene ring has 10 ⁇ electrons and an acridine group has 14 ⁇ electrons.
  • a benzene ring has 6 ⁇ electrons
  • a naphthylene ring has 10 ⁇ electrons
  • an acridine group has 14 ⁇ electrons.
  • Formula (6) wherein independently each variable,
  • amine having at least 3 or 4 aromatic groups may be represented by Formula (6a): wherein independently each variable,
  • the compound of Formula (6a) may also be represented by: wherein each variable U, R 1 , and R 2 are the same as described above and w may be 0 to 9 or 0 to 3 or 0 to 1 (typically 0).
  • Examples of an amine having at least 3 or 4 aromatic groups may be represented by any of the following Formulae (7) and/or (8): or
  • the amine having at least 3 or 4 aromatic groups may include mixtures of compounds represented by the formulae disclosed above.
  • compounds of Formulae (7) and (8) may also react with the aldehyde described below to form acridine derivatives.
  • Acridine derivatives that may be formed include compounds illustrated represented by Formula (7a) or (8a) to (8c) below.
  • a person skilled in the art will also appreciate that other acridine structures may be possible where the aldehyde reacts with other with benzyl groups bridged with the >NH group.
  • Examples of acridine structures include those represented by Formulae (7a), (8a) or (8b) or (8c): Any or all of the N-bridged aromatic rings are capable of such further condensation and perhaps aromaticisation.
  • One other of many possible structures include Formula (8b):
  • Examples of the amine having at least 3 or 4 aromatic groups may be bis[p-(p-aminoanilino)phenyl]-methane, 2-(7-amino-acridin-2-ylmethyl)-N-4- ⁇ 4-[4-(4-amino-phenylamino)-benzyl]-phenyl ⁇ -benzene-1,4-diamine, N-4- ⁇ 4-[4-(4-amino-phenylamino)-benzyl]-phenyl ⁇ -2-[4-(4-amino-phenylamino)-cyclohexa-1,5-dienylmethyl]-benzene-1,4-diamine, N-[4-(7-amino-acridin-2-ylmethyl)-phenyl]-benzene-1,4-diamine, or mixtures thereof.
  • the amine having at least 3 or 4 aromatic groups may be bis[p-(p-aminoanilino)phenyl]-methane, 2-(7-amino-acridin-2-ylmethyl)-N-4- ⁇ 4-[4-(4-amino-phenylamino)-benzyl]-phenyl ⁇ -benzene-1,4-diamine or mixtures thereof.
  • the amine having at least 3 or 4 aromatic groups may be prepared by a process comprising reacting an aldehyde with an amine (typically 4 aminodiphenylamine).
  • the resultant amine may be described as an alkylene coupled amine having at least 3 or 4 aromatic groups, at least one -NH 2 functional group, and at least 2 secondary or tertiary amino groups.
  • the aldehyde may be aliphatic, alicyclic or aromatic.
  • the aliphatic aldehyde may be linear or branched.
  • Examples of a suitable aromatic aldehyde include benzaldehyde or o-vanillin.
  • Examples of an aliphatic aldehyde include formaldehyde (or a reactive equivalent thereof such as formalin or paraformaldehyde), ethanal or propanal.
  • the aldehyde may be formaldehyde or benzaldehyde.
  • the amine having at least 3 or 4 aromatic groups may also be prepared by the methodology described in Berichte der Deutschen Chemischenmaschine (1910), 43, 728-39 .
  • the amine having at least 3 or 4 aromatic groups may be obtained/obtainable by a process comprising reacting isatoic anhydride or alkyl substituted isatoic anhydride, with an aromatic amine with at least two aromatic groups and a reactive primary or secondary amino group.
  • the resultant material may be described as an anthranilic derivative.
  • the anthranilic derivative may be prepared in a reaction containing isatoic anhydride or alkyl substituted isatoic anhydride and an aromatic amine selected from the group consisting of xylylenediamine, 4-aminodiphenylamine, 1,4-dimethylphenylenediamine, and mixtures thereof.
  • the aromatic amine may be 4-aminodiphenylamine.
  • the process described above to prepare the anthranilic derivative may be carried out at a reaction temperature in the range of 20°C to 180°C, or 40°C to 110°C.
  • the process may or may not be carried out in the presence of a solvent.
  • a suitable solvent include water, diluent oil, benzene, t-butyl benzene, toluene, xylene, chlorobenzene, hexane, tetrahydrofuran, or mixtures thereof.
  • the reactions may be performed in either air or an inert atmosphere. Examples of suitable inert atmosphere include nitrogen or argon, typically nitrogen.
  • the lubricating composition also comprises a dispersant viscosity modifier.
  • the lubricating composition comprises 0.1 to 1.2 wt % dispersant viscosity modifier.
  • the lubricating composition comprises 0.1 to 1.2 wt % of a dispersant viscosity modifier as described herein that has a number average molecular weight of at least 20,000.
  • the dispersant viscosity modifier may include functionalized polyolefins, for example, ethylene-propylene copolymers that have been functionalized with an acylating agent such as maleic anhydride and an amine; polymethacrylates functionalized with an amine, or styrene-maleic anhydride copolymers reacted with an amine. More detailed description of dispersant viscosity modifiers are disclosed in International Publication WO2006/015130 or U.S. Patents 4,863,623 ; 6,107,257 ; 6,107,258 ; 6,117,825 ; and US 7,790,661 . In one embodiment the dispersant viscosity modifier may include those described in U.S. Patent 4,863,623 (see column 2, line 15 to column 3, line 52) or in International Publication WO2006/015130 (see page 2, paragraph [0008] and preparative examples are described paragraphs [0065] to [0073]).
  • an acylating agent such as male
  • the dispersant viscosity modifier comprises an olefin copolymer further functionalized with a dispersant amine group.
  • the olefin copolymer may be an ethylene-propylene copolymer.
  • the dispersant amine group may be prepared/derived from reacting the olefin copolymer (typically, an ethylene-propylene copolymer) with an acylating agent (typically maleic anhydride) and an aromatic amine having a primary or secondary amino group.
  • the dispersant viscosity modifier may be an ethylene-propylene copolymer acylated with maleic anhydride and reacted with an aromatic amine.
  • the formation of a dispersant viscosity modifier is well known in the art.
  • the dispersant viscosity modifier may include for instance those described in U.S. Patent US 7,790,661 column 2, line 48 to column 10, line 38.
  • the dispersant viscosity modifier may be prepared by grafting of an olefinic carboxylic acid acylating agent onto a polymer of 15 to 80 mole percent of ethylene, from 20 to 85 mole percent of C 3-10 ⁇ -monoolefin, and from 0 to 15 mole percent of non-conjugated diene or triene, said polymer having an average molecular weight ranging from 5000 to 500,000, and further reacting said grafted polymer with an amine (typically an aromatic amine).
  • an amine typically an aromatic amine
  • the aromatic amine of the dispersant viscosity modifier may also include those which can be represented by the general structure NH 2 -Ar or T-NH-Ar, where T may be alkyl or aromatic, Ar may be an aromatic group, including nitrogen-containing or amino-substituted aromatic groups and Ar groups including any of the following structures as well as multiple non-condensed or linked aromatic rings.
  • Aromatic amines include those amines wherein a carbon atom of the aromatic ring structure is attached directly to the amino nitrogen.
  • the amines may be monoamines or polyamines.
  • the aromatic ring will typically be a mononuclear aromatic ring (i.e., one derived from benzene) but can include fused aromatic rings, especially those derived from naphthalene.
  • aromatic amines examples include aniline, N-alkylanilines such as N-methylaniline and N-butylaniline, di-(para-methylphenyl)amine, 4-aminodiphenylamine, N,N-dimethylphenylenediamine, naphthylamine, 4-(4-nitrophenylazo)aniline (disperse orange 3), sulphamethazine, 4-phenoxyaniline, 3-nitroaniline, 4-aminoacetanilide (N-(4-aminophenyl)acetamide)), 4-amino-2-hydroxy-benzoic acid phenyl ester (phenyl amino salicylate), N-(4-amino-phenyl)-benzamide, various benzylamines such as 2,5-dimethoxybenzylamine, 4-phenylazoaniline, and substituted versions of these.
  • N-alkylanilines such as N-methylaniline and N-butylaniline
  • aromatic amines include amino-substituted aromatic compounds and amines in which the amine nitrogen is a part of an aromatic ring, such as 3-aminoquinoline, 5-aminoquinoline, and 8-aminoquinoline.
  • aromatic amines such as 2-aminobenzimidazole, which contains one secondary amino group attached directly to the aromatic ring and a primary amino group attached to the imidazole ring.
  • Other amines include N-(4-anilinophenyl)-3-aminobutanamide or 3-amino propyl imidazole.
  • Yet other amines include 2,5-dimethoxybenzylamine.
  • Additional aromatic amines and related compounds are disclosed in U.S. Patent 6,107,257 and 6,107,258 ; some of these include aminocarbazoles, benzoimidazoles, aminoindoles, aminopyrroles, amino-indazolinones, aminoperimidines, mercaptotriazoles, aminophenothiazines, aminopyridines, aminopyrazines, aminopyrimidines, pyridines, pyrazines, pyrimidines, aminothiadiazoles, aminothiothiadiazoles, and aminobenzotriaozles.
  • aminocarbazoles include aminocarbazoles, benzoimidazoles, aminoindoles, aminopyrroles, amino-indazolinones, aminoperimidines, mercaptotriazoles, aminophenothiazines, aminopyridines, aminopyrazines, aminopyrimidines, pyridines, pyrazines, pyrimidines, aminothiadiazoles,
  • Suitable amines include 3-amino-N-(4-anilinophenyl)-N-isopropyl butanamide, and N-(4-anilinophenyl)-3- ⁇ (3-aminopropyl)-(cocoalkyl)amino ⁇ butanamide.
  • Other aromatic amines which can be used include various aromatic amine dye intermediates containing multiple aromatic rings linked by, for example, amide structures. Examples include materials of the general structure: and isomeric variations thereof, where R viii and R ix are independently alkyl or alkoxy groups such as methyl, methoxy, or ethoxy. In one instance, R viii and R ix are both -OCH 3 and the material is known as Fast Blue RR [CAS# 6268-05-9].
  • R ix may be -OCH 3 and R viii may be -CH 3 , and the material is known as Fast Violet B [99-21-8]. When both R viii and R ix are ethoxy, the material is Fast Blue BB [120-00-3].
  • U.S. Patent 5,744,429 discloses other aromatic amine compounds, particularly aminoalkylphenothiazines. N-aromatic substituted acid amide compounds, such as those disclosed in U.S. Patent Application 2003/0030033 A1 , may also be used for the purposes of the disclosed technology. Suitable aromatic amines include those in which the amine nitrogen is a substituent on an aromatic carboxyclic compound, that is, the nitrogen is not sp 2 hybridized within an aromatic ring.
  • the aromatic amine may also comprise an amine formed by reacting an aldehyde with 4-aminodiphenylamine.
  • the resultant amine may be described as an alkylene coupled amine having at least 4 aromatic groups, at least one -NH 2 functional group, and at least 2 secondary or tertiary amino groups.
  • the aldehyde may be aliphatic, alicyclic or aromatic.
  • the aliphatic aldehyde may be linear or branched.
  • Examples of a suitable aromatic aldehyde include benzaldehyde or o-vanillin.
  • Examples of an aliphatic aldehyde include formaldehyde (or a reactive equivalent thereof such as formalin or paraformaldehyde), ethanal or propanal.
  • the aldehyde may be formaldehyde or benzaldehyde.
  • this aromatic amine may also be prepared by the methodology described in Berichte der Deutschen Chemischen Deutschen Chemischen Deutschen Chemischen
  • the aromatic amine includes 4-aminodiphenylamine, aldehyde (typically formaldehyde) coupled 4-aminodiphenylamine, nitro-aniline (3- nitro-aniline), disperse orange-3 (DO3), or mixtures thereof.
  • the lubricating composition comprises a dispersant viscosity modifier derived from a polyolefin having a number average molecular weight of at least 20,000.
  • the lubricating composition may contain a mixture of low molecular weight and high molecular weight dispersant viscosity modifiers, provided that the overall number average molecular weight of the dispersant viscosity modifier is at least 20,000.
  • low molecular weight dispersant viscosity modifiers are derived from polyolefin copolymers having a number average molecular weight below 20,000, or even 10,000 or lower.
  • High molecular weight dispersant viscosity modifiers are derived from polyolefin copolymers having a number average molecular weight of greater than 20,000, or even 40,000 or greater, or even 45,000 or greater, such as 40,000 to 1,000,000.
  • the lubricating composition of the present invention may comprise a dispersant visocisty modifier wherein the dispersant viscosisty modifier comprises a mixture of at least one low molecular weight dispersant viscosity modifier derived from a polyolefin having a number average molecular weight of less than 20,000, and at least one high molecular weight dispersant viscosity modifier derived from a polyolefin having a number average molecular weight of at least 40,000.
  • the low molecular weight dispersant vicosity modifier may be derived from a polyolefin having a number average molecular weight of 10,000.
  • the high molecular weight dispersant viscosity modifier may be derived from a polyolefin having a number average molecular weight of 45,000 or greater.
  • the lubricating composition of the disclosed technology optionally comprises other performance additives.
  • the other performance additives include at least one of antioxidants, metal deactivators, viscosity modifiers, friction modifiers, antiwear agents, corrosion inhibitors, extreme pressure agents, foam inhibitors, demulsifiers, pour point depressants, seal swelling agents and mixtures thereof.
  • fully-formulated lubricating oil will contain one or more of these performance additives.
  • the lubricating composition optionally further includes at least one antiwear agent.
  • suitable antiwear agents include titanium compounds, esters, amides, and/or imides of alpha-hydroxycarboxylic acids (such as tartaric acid, malic acid, citric acid, glycolic acid), oil soluble amine salts of phosphorus compounds, sulfurized olefins, metal dihydrocarbyldithiophosphates (such as zinc dialkyldithiophosphates), phosphites (such as dibutyl phosphite), phosphonates, thiocarbamate-containing compounds, such as thiocarbamate esters, thiocarbamate amides, thiocarbamic ethers, alkylene-coupled thiocarbamates, and bis(S-alkyldithiocarbamyl) disulfides.
  • alpha-hydroxycarboxylic acids such as tartaric acid, malic acid, citric acid, glycolic acid
  • oil soluble amine salts of phosphorus compounds such as tartaric acid, malic acid
  • the antiwear agent may in one embodiment include a tartrate, or tartrimide as disclosed in International Publication WO 2006/044411 or Canadian Patent CA 1 183 125 .
  • the tartrate or tartrimide may contain alkyl-ester groups, where the sum of carbon atoms on the alkyl groups may be at least 8.
  • the antiwear agent may in one embodiment include a citrate as is disclosed in US Patent Application 20050198894 .
  • oil-soluble titanium compounds as disclosed in US 7,727,943 and US2006/0014651 .
  • the oil-soluble titanium compounds may function as antiwear agents, friction modifiers, antioxidants, deposit control additives, or more than one of these functions.
  • the oil soluble titanium compound may be a titanium (IV) alkoxide.
  • the titanium alkoxide may be formed from a monohydric alcohol, a polyol or mixtures thereof.
  • the monohydric alkoxides may have 2 to 16, or 3 to 10 carbon atoms.
  • the titanium alkoxide may be titanium (IV) isopropoxide.
  • the titanium alkoxide may be titanium (IV) 2-ethylhexoxide.
  • the titanium compound comprises the alkoxide of a vicinal 1,2-diol or polyol.
  • the 1,2-vicinal diol comprises a fatty acid mono-ester of glycerol, often the fatty acid may be oleic acid.
  • the oil soluble titanium compound may be a titanium carboxylate.
  • the titanium (IV) carboxylate may be titanium neodecanoate.
  • the lubricating composition may in one embodiment further include a phosphorus-containing antiwear agent.
  • a phosphorus-containing antiwear agent may be a zinc dialkyldithiophosphate, phosphite, phosphate, phosphonate, and ammonium phosphate salts, or mixtures thereof.
  • Zinc dialkyldithiophosphates are known in the art.
  • the lubricating composition may further include a phosphorus-containing antiwear agent based upon zinc dialkyldithiophosphate, or mixtures thereof.
  • the zinc dialkyldithiophosphate may be derived from aliphatic or aromatic hydrocarbyl alcohols; the hydrocarbyl; alcohols may be primary or secondary alcohols.
  • a zinc dialkyldithiophosphate (or ZDDP) derived from secondary alcohols is said to be a secondary ZDDP.
  • a ZDDP derived from primary alcohols is said to be a primary ZDDP.
  • ZDDP prepared from a mixture of primary and secondary alcohols is said to be a mixed primary/secondary ZDDP.
  • the ZDDP may be represented by the following structure: wherein each R may be independently a primary or secondary hydrocarbyl group containing from 1 to 24, for example from 2 to 12 carbon atoms and including groups such as alkyl, alkenyl, aryl, arylalkyl, alkaryl and cycloaliphatic hydrocarbyl groups.
  • R may be alkyl groups of 2 to 8 carbon atoms.
  • R may be an alkyl group having 5 or more carbon atoms.
  • R may be, for example, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, sec-butyl, amyl, n-hexyl, i-hexyl, n-octyl, decyl, dodecyl, octadecyl, 2-ethylehexyl, phenyl, butylphenyl, cyclohexyl, methylcyclopentyl, propenyl, and butenyl.
  • the R group of the zinc dithiophosphate may be derived, for example, from a primary alcohol such as methanol, ethanol, propanol, butanol, pentanol, hexanol, heptanol, octanol, nonanol, decanol, dodecanol, octadecanol, propenol, butenol, 2-ethylhexanol: a secondary alcohol such as isopropyl alcohol, secondary butyl alcohol, isobutanol, 3-methylbutan-2-ol, 2-pentanol, 4-methyl-2-pentanol, 2-hexanol, 3-hexanol, amyl alcohol, an aryl alcohol such as phenol, substituted phenol (particularly alkylphenol such as butylphenol, octylphenol, nonylphenol, dodecylphenol), disubstituted phenol.
  • a primary alcohol such as
  • Certain primary diols may also be used to prepare ZDDP; suitable primary diols include ethylene glycol, propylene gycol, and esters of polyhydric alcohol such as glycerol monooleate and combinations thereof.
  • ZDDP may be prepared from a combination of primary alcohols and primary diols.
  • the R group of the ZDDP may be independently a primary alkyl, a secondary alkyl, an aryl group, or mixtures thereof.
  • the R group of the ZDDP may be a secondary alkyl group.
  • the amount of metal dialkyldithiophosphate is present in amounts sufficient to deliver 0.1 wt % or less phosphorous to the lubrcating composition.
  • the lubricating composition comprises less than 0.1 wt % phosphorous.
  • the lubricating composition comprises 0.08 wt % or less phosphorous, for example 0.01 wt %, to 0.08 wt %.
  • the lubricating composition comprises a metal dialkyldithiophosphate such as ZDDP, wherein the alkyl groups in the metal dalkyldithiophosphate have 5 or more carbon atoms.
  • the lubricating composition of the present invention comprises a metal dialkyldithiophosphate wherein at least about 65 mol % or even 75 mol % of the alkyl groups have 5 or more carbon atoms.
  • the lubricating composition comprises a metal dialkyldithiophosphate wherein at least about 65 mol % or even 75 mol % of the alkyl groups have 5 or more carbon atoms, such as 5 to 24 carbon atoms, or even 5 to 12 carbon atoms, or even 6 to 12 carbon atoms, and wherein the lubricating composition comprieses 1 wt % to 4 wt % of a polyisobutenyl succinimide dispersant.
  • the friction modifier may be chosen from long chain fatty acid derivatives of amines, long chain fatty esters, or derivatives of long chain fatty epoxides; fatty imidazolines; amine salts of alkylphosphoric acids; fatty alkyl tartrates; fatty alkyl tartrimides; fatty alkyl tartramides; fatty glycolates; and fatty glycolamides.
  • the friction modifier may be present at 0 wt % to 6 wt %, or 0.01 wt % to 4 wt %, or 0.05 wt % to 2 wt %, or 0.1 wt % to 2 wt % of the lubricating composition.
  • fatty alkyl or "fatty” in relation to friction modifiers means a carbon chain having 10 to 22 carbon atoms, typically a straight carbon chain.
  • Suitable friction modifiers include long chain fatty acid derivatives of amines, fatty esters, or fatty epoxides; fatty imidazolines such as condensation products of carboxylic acids and polyalkylene-polyamines; amine salts of alkylphosphoric acids; fatty alkyl tartrates; fatty alkyl tartrimides; fatty alkyl tartramides; fatty phosphonates; fatty phosphites; borated phospholipids, borated fatty epoxides; glycerol esters; borated glycerol esters; fatty amines; alkoxylated fatty amines; borated alkoxylated fatty amines; hydroxyl and polyhydroxy fatty amines including tertiary hydroxy fatty amines; hydroxy alkyl amides; metal salts of fatty acids; metal salts of alkyl salicylates; fatty oxazolines; fatty ethoxylated alcohols; condensation products
  • Friction modifiers may also encompass materials such as sulfurized fatty compounds and olefins, molybdenum dialkyldithiophosphates, molybdenum dithiocarbamates, sunflower oil or soybean oil monoester of a polyol and an aliphatic carboxylic acid.
  • the friction modifier may be a long chain fatty acid ester.
  • the long chain fatty acid ester may be a mono-ester and in another embodiment the long chain fatty acid ester may be a triglyceride.
  • Extreme Pressure (EP) agents include compounds that are soluble in the oil include sulfur- and chlorosulfur-containing EP agents, dimercaptothiadiazole or CS 2 derivatives of dispersants (typically succinimide dispersants), derivative of chlorinated hydrocarbon EP agents and phosphorus EP agents.
  • EP agents include chlorinated wax; sulfurized olefins (such as sulfurized isobutylene), a hydrocarbyl-substituted 2,5-dimercapto-1,3,4-thiadiazole, or oligomers thereof, organic sulfides and polysulfides such as dibenzyldisulfide, bis-(chlorobenzyl) disulfide, dibutyl tetrasulfide, sulfurized methyl ester of oleic acid, sulfurized alkylphenol, sulfurized dipentene, sulfurized terpene, and sulfurized Diels-Alder adducts; phosphosulfurized hydrocarbons such as the reaction product of phosphorus sulfide with turpentine or methyl oleate; phosphorus esters such as the dihydrocarbon and trihydrocarbon phosphites, e.g., dibutyl phosphite, diheptyl phosphit
  • Foam inhibitors that may be useful in the compositions of the disclosed technology include polysiloxanes, copolymers of ethyl acrylate and 2-ethylhexylacrylate and optionally vinyl acetate; demulsifiers including fluorinated polysiloxanes, trialkyl phosphates, polyethylene glycols, polyethylene oxides, polypropylene oxides and (ethylene oxide-propylene oxide) polymers.
  • Pour point depressants that may be useful in the compositions of the disclosed technology include polyalphaolefins, esters of maleic anhydride-styrene copolymers, poly(meth)acrylates, polyacrylates or polyacrylamides.
  • Demulsifiers include trialkyl phosphates, and various polymers and copolymers of ethylene glycol, ethylene oxide, propylene oxide, or mixtures thereof.
  • Metal deactivators include derivatives of benzotriazoles (typically tolyltriazole), 1,2,4-triazoles, benzimidazoles, 2-alkyldithiobenzimidazoles or 2-alkyldithiobenzothiazoles.
  • the metal deactivators may also be described as corrosion inhibitors.
  • Seal swell agents include sulpholene derivatives Exxon Necton-37 TM (FN 1380) and Exxon Mineral Seal Oil TM (FN 3200).
  • the lubricating composition may be used for the lubrication of any of a variety of mechanical equipment types, including, but not limited to, an internal combusion engine, by supplying thereto the lubricating composition as described herein.
  • the engine may be a diesel (compression ignited) engine, such as a heavy duty diesel engine.
  • Other possible engines include gasoline (spark-ignited) engines, and engines consuming alcohols, gasoline-alcohol mixtures, biodiesel fuels, various mixed fuels, synthetic fuels, or gaseous fuels such as natural gas or hydrogen, two-stroke cycle engines, and marine diesel engines.
  • the internal combustion engine disclosed herein may have a steel surface on a cylinder bore, cylinder block, or piston ring.
  • the internal combustion engine may have a surface of steel, or an aluminium alloy, or an aluminium composite.
  • the compression-ignition internal combustion engine has a maximum laden mass over 3,500 kg.
  • the compression-ignition internal combustion engine may be referred to as a heavy duty diesel engine.
  • the laden mass (sometimes referred to as gross vehicle weight rating (GVWR)) may be over 2,700 kg (or 6,000 USA pounds) 2,900 kg, or over 3,00 kg, or over 3,300 kg, or over 3,500 kg, or over 3,700 kg, or over 3,900 kg (or 8,500 USA pounds).
  • GVWR gross vehicle weight rating
  • the upper limit on the laden mass or GVWR may be set by national government and may be 10,000 kg, or 9,000 kg, or 8,000 kg, or 7,500 kg.
  • the upper ranges of laden mass may be up to 400,000 kg, or up to 200,000 kg, or up to 60,000 kg, or up to 44,000 kg, or up to 40,000 kg.
  • a laden mass above 120,000 may be for an off-highway vehicle.
  • Heavy duty diesel engines are noted to be limited to all motor vehicles with a “technically permissible maximum laden mass” over 3,500 kg, equipped with compression ignition engines or positive ignition natural gas (NG) or LPG engines.
  • NG positive ignition natural gas
  • LPG low-duty truck
  • the internal combustion engine may be a heavy duty diesel compression ignited (or spark assisted compression ignited) internal combustion engine.
  • the lubricating composition is formulated containing the components and combinations of components as described herein.
  • the lubricating composition is formulated as a high-temperature high shear fluid having a dynamic visocisty of less than 3.5 cP, or even less than 3.1 cP, or even less than 3.05 cP as meaured according to ASTM D4683 at 150 °C.
  • the lubricating composition is formulated to have a kinematic viscosity at 100 °C of 10 cSt or lower as measured according to ASTM D445-17.
  • Example 1 Example 2
  • Example 3 Example 4
  • Example 5 10W-30 10W-30 10W-30 10W-30 10W-30 Group II Base Oil x x x x x x x Group III Base Oil x GTL Base Oil x x HV-dispersant 0.7
  • Other succinimide dispersant 3.6 4.4 3.7 3.7 3.4 ZDDP 1 (C3/C6) 0.68 1.0 1.0 1.0 0.18 ZDDP 2 (C6 2°) 0.6
  • Ashless Antioxidant (combo of aminic and phenolic) 2.5 1.37 2.7 2.3 2.75
  • Example 6 Example 7
  • Example 8 Example 9
  • Example 10 Example 11 5W-30 5W-30 5W-30 5W-30 5W-30 5W-30 5W-30 Group III Base Oil x x GTL Base Oil x x X X PAO X HV-dispersant 1.4 1.4 1.4 1.4 1.4
  • Other succinimide dispersant 3.7 3.7 3.7 3.7 3.7 3.4 ZDDP 1 (C3/C6) 0.68 0.18 0.68 0.68 0.18 0.18 ZDDP 2 (C6) 0.6 0.6 0.6
  • High TBN Mg Sulfonate 0.42 0.38 S-coupled Phenate 0.29 0.29 0.29 Methylene coupled phenate 1 (Mg saligenin) 0.25 0.37 Methylene coupled phenate 2 (Ca salixarate) 0.45 0.45 0.45 0.45 Ashless Antioxidant (combo of
  • the transitional term "comprising”, which is synonymous with “including”, “containing”, or “characterized by”, is inclusive or open-ended and does not exclude additional, un-recited elements or method steps.
  • the term also encompass, as alternative embodiments, the phrases “consisting essentially of' and “consisting of', where “consisting of' excludes any element or step not specified and “consisting essentially of” permits the inclusion of additional un-recited elements or steps that do not materially affect the basic, essential and novel characteristics of the composition or method under consideration.
  • the phrase “substantially free of' means that the compposition or component may include trace or contaminant amounts of a material, but that such materials are not added in functional amounts.
  • compression ignited internal combustion engine is intended to encompass internal combustion engines that has at least in part compression ignition.
  • the disclosed technology is intended to encompass a method of lubricating a compression ignited internal combustion engine, as well as spark assisted compression ignited internal combustion engines.
  • hydrocarbyl substituent or “hydrocarbyl group” is used in its ordinary sense, which is well-known to those skilled in the art. Specifically, it refers to a group having a carbon atom directly attached to the remainder of the molecule and having predominantly hydrocarbon character.
  • hydrocarbyl groups include: hydrocarbon substituents, including aliphatic, alicyclic, and aromatic substituents; substituted hydrocarbon substituents, that is, substituents containing non-hydrocarbon groups which, in the context of this invention, do not alter the predominantly hydrocarbon nature of the substituent; and hetero substituents, that is, substituents which similarly have a predominantly hydrocarbon character but contain other than carbon in a ring or chain.
  • the number average molecular weight of the dispersant viscosity modifier and viscosity modifier has been determined using known methods, such as GPC analysis using polystyrene standards.
  • Methods for determining molecular weights of polymers are well known. The methods are described for instance: (i) P.J. Flory, “Principles of Polymer Chemistry", Cornell University Press 91953), Chapter VII, pp 266-315 ; or (ii) " Macromolecules, an Introduction to Polymer Science", F. A. Bovey and F. H. Winslow, Editors, Academic Press (1979), pp 296-312 .

Claims (11)

  1. Procédé de réduction de l'usure par adhérence d'un moteur à combustion lubrifié avec une composition lubrifiante à faible teneur en phosphore, comprenant la fourniture au moteur d'une composition lubrifiante comprenant moins de 0,1 % en poids de phosphore et présentant une viscosité de 10 centistokes ou moins à 100 °C mesurée conformément à la norme ASTM D445-17, comprenant :
    a) une huile de viscosité de lubrification ;
    b) un ou plusieurs détergents sans soufre contenant un métal dérivés d'un alkylphénol en une quantité permettant de fournir au moins 0,2 % en poids de savon contenant de l'alkylphénol à la composition ;
    c) un ou plusieurs détergents à base de sulfonate de métal alcalino-terreux en une quantité permettant de fournir au moins 0,8 % en poids de savon sulfonate à la composition ;
    d) 1 % en poids à 4,5 % en poids d'un ou de plusieurs dispersants polyisobutylène succinimide ; et
    e) 0,1 % en poids à 1,2 % en poids d'un modificateur de viscosité d'un dispersant dérivé d'une polyoléfine présentant un poids moléculaire moyen en nombre d'au moins 20 000 ;
    la composition lubrifiante contenant moins de 0,2 pourcentage en poids d'un détergent phénate couplé au soufre.
  2. Procédé selon la revendication 1, dans lequel la composition lubrifiante comprend moins de 0,15 % en poids d'un détergent phénate couplé au soufre.
  3. Procédé selon l'une quelconque des revendications 1 ou 2, dans lequel le modificateur de viscosité de dispersant comprend un mélange d'au moins un modificateur de viscosité de dispersant de faible poids moléculaire, dérivé d'une polyoléfine présentant un poids moléculaire moyen en nombre inférieur à 20 000 et d'au moins un modificateur de viscosité de dispersant de poids moléculaire élevé, dérivé d'une polyoléfine présentant un poids moléculaire moyen en nombre d'au moins 40 000.
  4. Procédé selon la revendication 3, dans lequel l'au moins un modificateur de viscosité de dispersant de faible poids moléculaire est dérivé d'une polyoléfine ayant un poids moléculaire moyen en nombre de 10 000 ou moins.
  5. Procédé selon la revendication 3 ou 4, dans lequel l'au moins un modificateur de viscosité de dispersant de poids moléculaire élevé est dérivé d'une polyoléfine ayant un poids moléculaire moyen en nombre d'au moins 45 000.
  6. Procédé selon l'une quelconque des revendications 1 à 5, dans lequel le détergent à base d'alkylphénol sans soufre est sélectionné parmi les détergents alkylphénols couplés à un alkylène, les détergents alkylsalicylates et leurs combinaisons.
  7. Procédé selon la revendication 6, dans lequel le détergent à base d'alkylphénol sans soufre comprend de la saligénine de Mg.
  8. Procédé selon la revendication 6, dans lequel le détergent à base d'alkylphénol sans soufre comprend du salixarate de Ca.
  9. Procédé selon l'une quelconque des revendications 1 à 8, comprenant en outre :
    un dialkyldithiophosphate de métal, dans lequel au moins 65 % en moles des groupes alkyle présentent au moins 5 atomes de carbone, présent en une quantité permettant de fournir 0,01 à 0,08 % en poids de phosphore à la composition.
  10. Procédé selon l'une quelconque des revendications 1 à 8, comprenant en outre :
    un dialkyldithiophosphate de métal, dans lequel au moins 75 % en moles des groupes alkyle présentent au moins 5 atomes de carbone, présent en une quantité permettant de fournir 0,01 à 0,08 % en poids de phosphore à la composition et dans lequel la composition comprend 1 % en poids à 4 % en poids d'un ou de plusieurs dispersants polyisobutylène succinimide.
  11. Procédé selon l'une quelconque des revendications 1 à 10, dans lequel la composition lubrifiante est un fluide à fort cisaillement et à haute température, présentant une viscosité dynamique inférieure à 3,05 à 150 °C, mesurée selon la norme ASTM D4683.
EP21150240.6A 2016-09-14 2017-08-28 Procédé de lubrification d'un moteur à combustion interne Active EP3851508B1 (fr)

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US201662394235P 2016-09-14 2016-09-14
EP17761777.6A EP3512926B1 (fr) 2016-09-14 2017-08-28 Composition lubrifiante et procédé de lubrification d'un moteur a combustion interne
PCT/US2017/048843 WO2018052692A1 (fr) 2016-09-14 2017-08-28 Composition lubrifiante et procédé de lubrification d'un moteur a combustion interne

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EP17761777.6A Division-Into EP3512926B1 (fr) 2016-09-14 2017-08-28 Composition lubrifiante et procédé de lubrification d'un moteur a combustion interne

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CN109790481A (zh) 2019-05-21
WO2018052692A1 (fr) 2018-03-22
US20190185778A1 (en) 2019-06-20
CA3036103A1 (fr) 2018-03-22
EP3512926A1 (fr) 2019-07-24
EP3512926B1 (fr) 2021-02-17

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