WO2013006303A1 - Lubrifiant fournissant une propreté améliorée pour des moteurs à deux temps - Google Patents

Lubrifiant fournissant une propreté améliorée pour des moteurs à deux temps Download PDF

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Publication number
WO2013006303A1
WO2013006303A1 PCT/US2012/044118 US2012044118W WO2013006303A1 WO 2013006303 A1 WO2013006303 A1 WO 2013006303A1 US 2012044118 W US2012044118 W US 2012044118W WO 2013006303 A1 WO2013006303 A1 WO 2013006303A1
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WIPO (PCT)
Prior art keywords
lubricant composition
percent
weight
dispersant
lubricant
Prior art date
Application number
PCT/US2012/044118
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English (en)
Inventor
Brent R. Dohner
Original Assignee
The Lubrizol Corporation
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Filing date
Publication date
Application filed by The Lubrizol Corporation filed Critical The Lubrizol Corporation
Priority to CA2841048A priority Critical patent/CA2841048A1/fr
Priority to JP2014518899A priority patent/JP2014522893A/ja
Priority to CN201280042936.XA priority patent/CN103857775A/zh
Priority to EP12735693.9A priority patent/EP2729555A1/fr
Priority to US14/130,720 priority patent/US20140130759A1/en
Publication of WO2013006303A1 publication Critical patent/WO2013006303A1/fr
Priority to IN114DEN2014 priority patent/IN2014DN00114A/en

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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
    • C10M141/00—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
    • C10M141/06—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic nitrogen-containing compound
    • 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
    • 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
    • C10M2203/1006—Petroleum or coal fractions, e.g. tars, solvents, bitumen used as base material
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/026—Butene
    • C10M2205/0265—Butene used as base material
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02—Hydroxy compounds
    • C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/26—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
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/28—Amides; Imides
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2217/043—Mannich bases
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/046—Overbasedsulfonic acid salts
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04—Phosphate esters
    • C10M2223/045—Metal containing thio derivatives
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • 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
    • C10N2030/40—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
    • C10N2030/52—Base number [TBN]
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00—Specified use or application for which the lubricating composition is intended
    • C10N2040/25—Internal-combustion engines
    • C10N2040/255—Gasoline engines
    • C10N2040/26—Two-strokes or two-cycle engines

Definitions

  • the disclosed technology relates to an engine lubricant, particularly for two- stroke cycle engines.
  • Two-stroke cycle engines are widely used for portable power equipment and also represent an important portion of the engines used in transportation, particularly in the developing regions of the world.
  • the lubricants required for the operation of two-stroke cycle engines are, in some designs, mixed with the liquid fuel, and this fuel-lubricant mixture is typically passed through the crankcase and, ultimately, to the combustion chambers, where the entire fuel-lubricant composition is burned. It is important, in such engines, to provide a lubricant composition which maintains suitable properties of lubricity and cleanliness. Problems with cleanliness can be observed as deposit or varnish formation within the engine in such areas as the piston skirt, the ring area of the piston, or the crank- case. It is desired to find an economical lubricant additive package that provides good cleanliness to a two-stroke cycle engine.
  • U.S. Publication 2011-0030637 Dohner et al., February 10, 201 1 (previously published as WO2009/126381, October 15, 2009), discloses a lubricant comprising, among other components, about 3 to about 30 percent by weight of a nitrogen-containing disper- sant bearing a hydrocarbyl group of at least 26 carbon atoms and having a nitrogen content of at least 3 percent by weight, wherein the nitrogen content of the lubricant is at least about 0.2 percent by weight.
  • the dispersant may be a succinimide dispersant.
  • the lubricant may further comprise about 1.1 to about 15 percent by weight of a Mannich dispersant.
  • a lubricant composition comprises, among other components, (A) an oil of lubricating viscosity and (B) an additive composition that comprises (1) a reaction product of a fatty hydrocarbyl-substituted monocarboxylic acylat- ing and a (select) reactive nitrogen-containing compound; and (2) a member selected from the group consisting of (a) a hydrocarbyl-substituted aminophenol; (b) a Mannich reaction product of a hydrocarbyl-substituted phenol, an aldehyde, and an amine; (c) a reaction product of a hydrocarbyl-substituted polycarboxylic acylating agent and a polyamine; and (d) a mixture thereof.
  • the hydrocarbyl-substituted polycarboxylic acylating agent can be a po lyisobutenylsuccinic anhydride .
  • U.S. Patent 7,795,192, Petric et al, September 14, 2010 discloses a lubricant composition suitable for lubricating a direct fuel injection two-stroke engine, comprising, among other components, a condensation product of a fatty hydrocarbyl monocarboxylic acid with a polyethylene polyamine, and a Mannich dispersant, being the reaction product of a polybutene-substituted phenol, formaldehyde, and ethylenediamine or dimethylamine.
  • the lubricant may further comprise an additional dispersant which may be, among others, a mono-succinimide dispersant.
  • U.S. Publication 2008-0009428 Svarcas et al., JanuarylO, 2008, discloses a lubricant composition suitable for lubricating a two stroke engine comprising an oil of lubricating viscosity, a synthetic ester, a normally liquid solvent, a Mannich dispersant, and a condensation product of a fatty acid having about 12 to about 24 carbon atoms with a polyamine.
  • a commercial two-cycle oil comprises, among other components, a fatty acid imidazole dispersant, and a succinimide dispersant.
  • the disclosed technology provides a lubricant composition
  • a lubricant composition comprising: (a) an oil of lubricating viscosity; (b) 0.1 to 2 percent by weight of a Mannich dispersant; and (c) 0.2 to 2 percent by weight of a succinimide dispersant; wherein the succinimide dispersant provides at least about 40 parts per million by weight of nitrogen atoms to the lubricant composition.
  • the lubricant composition further comprises (d) a metal- containing detergent.
  • the disclosed technology also provides a method of lubricating an internal combustion engine, such as a two-stroke cycle engine, comprising supplying thereto the lubricant composition.
  • One component of the disclosed technology is an oil of lubricating viscosity, also referred to as a base oil.
  • the base oil may be selected from any of the base oils in
  • Group I >0.03 and/or ⁇ 90 80 to 120
  • PAOs polyalphaolefms
  • Groups I, II and III are mineral oil base stocks.
  • the oil of lubricating viscosity can include natural or synthetic oils and mixtures thereof. Mixture of mineral oil and synthetic oils, e.g., polyalphaolefm oils and/or polyester oils, may be used.
  • the oil will be a mineral oil, that is, Group I, II, or III, and in some embodiments it will be a Group II oil or a Group III oil.
  • Natural oils include animal oils and vegetable oils (e.g. vegetable acid esters) as well as 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. Hydrotreated or hydrocracked oils are also useful oils of lubricating viscosity. Oils of lubricating viscosity derived from coal or shale are also useful.
  • Synthetic oils include hydrocarbon oils and halosubstituted hydrocarbon oils such as polymerized and interpolymerized olefins and mixtures thereof, alkylbenzenes, polyphenyl, alkylated diphenyl ethers, and alkylated diphenyl sulfides and their derivatives, analogs and homologues thereof.
  • Alkylene oxide polymers and interpolymers and derivatives thereof, and those where terminal hydro xyl groups have been modified by, e.g., esterification or etherification, are other classes of synthetic lubricating oils.
  • suitable synthetic lubricating oils comprise esters of dicarboxylic acids and those made from C5 to C 12 monocarboxylic acids and polyols or polyol ethers.
  • Other synthetic lubricating oils include liquid esters of phosphorus-containing acids, polymeric tetrahydrofurans, silicon- based oils such as poly-alkyl-, polyaryl-, polyalkoxy-, or polyaryloxy-siloxane oils, and silicate oils.
  • oils include those produced by Fischer-Tropsch reactions, typically hydroisomerized Fischer-Tropsch hydrocarbons or waxes.
  • oils may be prepared by a Fischer-Tropsch gas-to-liquid synthetic procedure as well as other gas-to-liquid oils.
  • Unrefined, refined and rerefmed oils either natural or synthetic (as well as mixtures thereof) of the types disclosed hereinabove can be used.
  • Unrefined oils are those obtained directly from a natural or synthetic source without 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.
  • Rerefmed oils are obtained by processes similar to those used to obtain refined oils applied to refined oils which have been already used in service. Rerefmed oils often are additionally processed to remove spent additives and oil breakdown products.
  • Another components that may be considered a part of the oil of lubricating viscosity includes bright stock (a high viscosity mineral oil fraction), which may be typically present, if desired, in amounts of 1 to 5 or 1.5 to 3 percent by weight.
  • the amount of oil of lubricating viscosity in a fully formulated lubricant of the disclosed technology will typically be 20 to 60 percent by weight, or 25 to 55 percent, or 30 to 50 percent by weight.
  • the lubricant will also include a Mannich dispersant and a succinimide disper- sant.
  • Dispersants in general are well known in the field of lubricants and include primarily what is known as ashless dispersants and polymeric dispersants. Ashless dispersants are so-called because, as supplied, they do not contain metal and thus do not normally contribute to sulfated ash when added to a lubricant. However they may, of course, interact with ambient metals once they are added to a lubricant which includes metal-containing species. Ashless dispersants are characterized by a polar group attached to a relatively high molecular weight hydrocarbon chain.
  • a Mannich dispersant is a reaction product of a hydrocarbyl-substituted phenol, an aldehyde, and an amine or ammonia.
  • the hydrocarbyl substituent of the hydrocarbyl-substituted phenol can have 10 to 400 carbon atoms, in another instance 30 to 180 carbon atoms, and in a further instance 10 or 40 to 110 carbon atoms.
  • This hydrocarbyl substituent can be derived from an olefin or a polyolefm.
  • Useful olefins include alpha-olefms, such as 1-decene, which are commercially available.
  • the polyolefms which can form the hydrocarbyl substituent can be prepared, for instance, by polymerizing olefin monomers by well-known polymerization methods and are also commercially available.
  • the olefin monomers include monoolefms, including monoolefms having 2 to 10 carbon atoms such as ethylene, propylene, 1-butene, isobutylene, and 1-decene.
  • An especially useful monoolefm source is a C4 refinery stream having a 35 to 75 weight percent butene content and a 30 to 60 weight percent isobutene content.
  • Useful olefin monomers also include diolefins such as isoprene and 1,3-butadiene.
  • Olefin monomers can also include mixtures of two or more monoolefms, of two or more diolefins, or of one or more monoolefms and one or more diolefins.
  • Useful polyolefms include polyisobutylenes having a number average molecular weight of 140 to 5000, in another instance of 400 to 2500, and in a further instance of 140 or 500 to 1500.
  • the polyisobutylene can have a vinylidene double bond content of 5 to 69%, in a second instance of 50 to 69%, and in a third instance of 50 to 95%.
  • the polyolefm can be a homopolymer prepared from a single olefin monomer or a copolymer prepared from a mixture of two or more olefin monomers.
  • the hydrocarbyl substituent source are mixtures of two or more homopolymers, two or more copolymers, or one or more homopolymers and one or more copolymers.
  • suitable hydrocarbyl groups or polyolefm groups is also applicable to the hydrocarbyl substituent of the succinimide dispersant, described in detail below.
  • the hydrocarbyl-substituted phenol which is used to prepare the Mannich dispersant can be prepared by alkylating phenol with an olefin or polyolefm described above, such as a polyisobutylene or polypropylene, using well-known alkylation methods.
  • the aldehyde used to form the Mannich dispersant can have 1 to 10 carbon atoms, and is generally formaldehyde or a reactive equivalent thereof such as formalin or paraformaldehyde.
  • the amine used to form the Mannich dispersant can be a monoamine or a polyamine, including those materials described above for the succinimide dispersants, including alkanolamines having one or more hydroxyl groups.
  • Useful amines include ethanolamine, diethanolamine, methylamine, dimethylamine, ethylenediamine, dimethyla- minopropylamine, diethylenetriamine and 2-(2-aminoethylamino)ethanol.
  • the Mannich dispersant can be prepared by reacting a hydrocarbyl-substituted phenol, an aldehyde, and an amine as described in U.S. Patent No. 5,697,988.
  • the Mannich reaction product is prepared from an alkylphenol derived from a polyisobutylene, formaldehyde, and an amine that is a primary monoamine, a secondary monoamine, or an al- kylenediamine, in particular, ethylenediamine or dimethylamine.
  • the alkylphenol may be prepared from a high-vinylidene polyisobutene, having, e.g., greater than 50, greater than 70 or greater than 75 percent terminal vinylidene groups (i.e., such percentage of polyisobutylene molecules having vinylidene end groups; that is, mole percentage of polyisobutylene molecules having a terminal vinylidene group.)
  • a high-vinylidene polyisobutene having, e.g., greater than 50, greater than 70 or greater than 75 percent terminal vinylidene groups (i.e., such percentage of polyisobutylene molecules having vinylidene end groups; that is, mole percentage of polyisobutylene molecules having a terminal vinylidene group.)
  • the foregoing description of the amine is also applicable to the description of the amine used in preparing the succinimide dispersant, described below.
  • the Mannich dispersant comprises the reaction product of a hydrocarbyl-substituted phenol, formaldehyde or a reactive equivalent of formaldehyde, and a primary or secondary amine. In one embodiment the Mannich dispersant comprises the reaction product of a polyisobutene-substituted phenol, formaldehyde or a reactive equivalent of formaldehyde, and dimethyl amine.
  • 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 amount of the Mannich dispersant will typically be 0.1 to 2 percent by weight of the lubricant composition. In other embodiments it may be present at 0.15 to 1.5 percent, or 0.2 to 1.05 percent, or 0.2 to 1 percent, or 0.3 to 0.6 percent by weight.
  • a second type of dispersant that will be present in the disclosed compositions is a succinimide dispersant.
  • the succinimide dispersant is a condensation product of hydrocarbyl-substituted succinic anhydride or a reactive equivalent thereof (e.g., an anhydride, ester, or acid halide), with a polyethylene polyamine.
  • Succinimide disper- sants may generally be viewed as comprising a variety of chemical structures including typically
  • each R is independently an alkyl group, frequently a polyisobutylene group with a molecular weight (M n ) of 500-5000 based on the polyisobutylene precursor, and R are alkylene groups, commonly ethylene (C 2 H 4 ) groups.
  • R are alkylene groups, commonly ethylene (C 2 H 4 ) groups.
  • Such molecules are commonly derived from reaction of an alkenyl acylating agent with a polyamine, and a wide variety of linkages between the two moieties is possible beside the simple imide structure shown above, including a variety of amides and quaternary ammonium salts.
  • the amine portion is shown as an alkylene polyamine, although other aliphatic and aromatic mono- and polyamines may also be used.
  • the ratio of the carbonyl groups of the acylating agent to the nitrogen atoms of the amine may be 1 :0.5 to 1 :3, and in other instances 1 : 1 to 1 :2.75 or 1 : 1.5 to 1 :2.5.
  • Succinimide disper- sants are more fully described in U.S. Patents 4,234,435 and 3,172,892 and in EP 0355895.
  • Succinimide dispersants may also be described as being prepared from hydro- carbyl-substituted succinic acylating agent which are, in turn, prepared by the so-called “chlorine” route or by the so-called “thermal” or “direct alkylation” route. These routes are described in detail in published application US 2005-0202981, paragraphs 0014 through 0017. A direct alkylation or low-chlorine route is also described in U.S. Patent 6,077,909; refer to column 6 line 13 through col. 7 line 62 and column 9 lines 10 through col. 10 line 11.
  • Illustrative thermal or direct alkylation processes involve heating a polyolefm, typical- ly at 180 to 250 °C, with maleic anhydride under an inert atmosphere. Either reactant may be in excess. If the maleic anhydride is present in excess, the excess may be removed after reaction by distillation.
  • These reactions may employ, as the polyolefm, high vinylidene polyisobutylene, that is, having greater than 50, 70, or 75% terminal vinylidene groups (a 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.
  • the succinimide dispersant will be one which is capable of providing a relatively large quantity of nitrogen to the lubricant.
  • the nitrogen will be nitrogen atoms that are a part of the amine component or the condensed amide or imide groups of the dispersant. That is, it will impart at least 40 parts per million by weight of nitrogen to the lubricant, and in some embodiments at least 70 or 100 or 130 or 150 parts per million, and up to, for example, 1000 or 900 or 800 or 600 parts per million. These amounts will be determined by both the amount of the succinimide dispersant in the lubricant formulation and the amount of nitrogen within the given dispersant.
  • certain of the succinimide dispersants of the present technology are comparatively high in nitrogen content, i.e., at least 3 percent or at least 4 percent or at least 4.4 percent by weight, and up to 6 or 5.5 or 5 percent.
  • Such high nitrogen dispersants are, in certain embodiments, characterized as having a high TBN, total base number (ASTM D 974), due to the presence of basic amine functionality.
  • the present succinimide dispersant may thus have a TBN of at least 90 or 100 or 110 and up to, for instance, 160 or 140 or 120.
  • Other suitable TBN ranges may be 60 to 160 or 70 to 140 or 80 to 120.
  • Such values are to be calculated on the basis of an oil- free dispersant, as will be evident to the skilled person.
  • the succin- imide dispersant may be borated.
  • the amount of the succinimide dispersant will typically be 0.1 to 2 percent by weight of the lubricant composition. In other embodiments it may be present at 0.15 to 1.5 percent, or 0.2 to 1 percent, or 0.3 to 0.6 percent by weight.
  • the relative amounts of the Mannich dispersant and the succinimide dispersant, expressed as a weight ratio, may be 80:20 to 20:80 or alternatively 70:30 to 30:70 or 65 :35 to 45:55.
  • the total amount of the Mannich dispersant and the succinimide dispersant, and optionally any other nitrogen- containing dispersants that may be present, may be 0.2 to 4 percent by weight, or 0.3 to 3 percent, or 0.4 to 2 percent.
  • dispersants may also be present, if desired. They may be lower nitrogen- content dispersants than the above-described succinimide dispersant, or they may have shorter or longer hydrocarbyl chains, or they may have other functional groups.
  • One such dispersant may be a condensation product of a fatty hydrocarbyl monocarboxylic acylating agent, such as a fatty acid, with an amine.
  • the fatty acid may contain 10 to 26 carbon atoms (e.g., 12 to 24 or 14 to 20 or 16 to 18).
  • An example is isostearic acid.
  • the amine may be a polyethylene polyamine as described above.
  • the condensation product may be an amide or an imidazoline.
  • Other dispersants include high molecular weight esters.
  • dispersants include polymer- ic dispersant additives, also referred to as dispersant viscosity modifiers, which are generally hydrocarbon-based polymers containing polar functionality to impart dispersancy characteristics to the polymer.
  • dispersant viscosity modifiers are generally hydrocarbon-based polymers containing polar functionality to impart dispersancy characteristics to the polymer.
  • Such post-treatment includes reaction with urea, thiourea, dimercaptothiadiazoles, carbon disulfide, aldehydes, ketones, carboxylic acids, hydrocarbon-substituted succinic anhydrides, nitriles, epoxides, boron compounds such as boric acid, phosphorus compounds, or mixtures thereof. References detailing such treatment are listed in U.S. Patent 4,654,403.
  • lubricants may also be present in the lubricants described herein, and in particular those materials which are desirable to provide a lubricant for a two-stroke cycle engine.
  • a solvent which may be used to aid in the solubility of the additives in the lubricant or in the fuel with which it is conventionally to be mixed or to adjust the viscosity parameters of the lubricant.
  • a combustible solvent other than oil of lubricating viscosity, described above, having a flash point of less than about 105°C, in which the remaining components of the lubricant are soluble.
  • the solvent is typically a hydro carbonaceous solvent, that is, one which exhibits principally hydrocarbon character, even though relatively small numbers of heteroatoms may be present in the molecule.
  • the solvent may be a hydrocarbon and may have predominantly non-aromatic (e.g., alkane) character.
  • the solvent may thus comprises less than 20 percent by weight aromatic components and may be substantially free from polynuclear aromatic components.
  • a particularly suitable solvent is kerosene, which is a non-aromatic petroleum distillate having a boiling range of 180-300°C.
  • Another useful solvent is Stoddard solvent, which has a boiling range of 154-202°C.
  • the solvent is characterized by a kinematic viscosity of less than 5 mm s " (cSt) at 100°C, such as less than 2.0 or 1.5 or 1.0 mm2s-l .
  • solvents are of lower viscosity than the oils of lubricating viscosity, which, accordingly, may have a kinematic viscosity of at least 1.0 or 1.5 or 2.0 or 5 mm s "1 at 100°C.
  • the amount of the solvent, if it is present, may be at least 5 percent by weight of the lubricant, or at least 10 percent, up to 50 or 40 or 30 percent. Suitable ranges may include combinations of the above values, or 15 to 30 percent by weight.
  • the lubricant composition may also contain a polymer such as polyisobutene, or, more generally, an olefin polymer.
  • Olefin polymers are well known as additives for two-stroke cycle engines. Generally they are relatively low molecular weight materials, having a molecular weight (number average) of 5000 or less, such as 500 to 3000 or 1000 to 2500. Occasionally, however, higher molecular weight olefin polymers have been used in two-cycle lubricants; see, for example, U.S. patent 5,741,764, Patel et al., April 21, 1991. Such polymers may be hydrogenated to remove most or all of any remaining ethylenic unsaturation.
  • an olefin copolymer such as a low molecular weight polyisobutylene
  • it may be present in an amount of up to 50 percent, such as 10 to 50 percent by weight or 15 to 45 percent or 20 to 40 percent or 25 to35 percent by weight.
  • hydrocarbyl-substituted phenol Another material which may be present is a hydrocarbyl-substituted phenol.
  • the hydrocarbyl-substituted phenol may be a polyisobutylene-substituted phenol, and the polyisobutylene group may have a number average molecular weight of 300 to 3000 or 500 to 2000 or 750 to 1600 or about 1000. It is believed that the presence of a hydrocarbyl-substituted phenol may provide some antioxidant performance to the lubricant.
  • the hydrocarbyl phenol if it is present, may be present, in an amount of up to 10 percent, such as 1 to 5 percent or 2 to 4 percent or 2.5 to 3.5 percent by weight.
  • the lubricant composition may also contain a detergent such as a metal- containing detergent.
  • a detergent such as a metal- containing detergent.
  • Detergents are often overbased materials, otherwise referred to as overbased or superbased salts. These are generally single phase, 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, preferably 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 said acidic organic material, a stoichiometric excess of a metal base, and a promoter such as a phenol or alcohol.
  • an acidic material typically an inorganic acid or lower carboxylic acid, preferably carbon dioxide
  • a reaction medium comprising at least one inert, organic solvent (e.g., mineral oil, naphtha, toluene, xylene) for said acidic organic material, a stoichiometric excess of a metal base, and a promoter such as a phenol or alcohol.
  • organic solvent e.g., mineral oil, naphtha, toluene, xylene
  • the acidic organic material will normally have a sufficient number of carbon atoms to provide a degree of solubility in oil.
  • the amount of excess metal is commonly expressed in terms of metal ratio.
  • the term "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.
  • Such overbased materials are well known to those skilled in the art. Patents describing techniques for making basic salts of alkylaromatic sulfonic acids, carboxylic acids, phenols, phosphonic acids, and mixtures of any two or more of these include U.S.
  • salixarate detergents include overbased materials prepared from salicylic acid (which may be unsubstituted) with a hydrocarbyl-substituted phenol, such entities being linked through -CH2- or other alkylene bridges.
  • salixarate derivatives have a predominantly linear, rather than macrocyclic, structure, although both structures are intended to be encompassed by the term "salixarate.”
  • 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.
  • the detergent may be an overbased sulfonate, phenate, salicylate, or salixarate detergent. In certain embodiments it may comprise an overbased calcium phenate detergent.
  • the phenols useful in making phenate detergents can be represented by (R 1 ) a -Ar-(OH) b , where R 1 is an aliphatic hydrocarbyl group of 4 to 400 or 6 to 80 or 6 to 30 or 8 to 25 or 8 to 15 carbon atoms; Ar is an aromatic group such as benzene, toluene or naphthalene; a and b are each at least one, the sum of a and b being up to the number of displaceable hydrogens on the aromatic nucleus of Ar, such as 1 to 4 or 1 to 2. There is typically 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 metal salt of the phenate detergent is typically calcium
  • the metal compounds useful in making the basic metal salts are more generally any Group 1 or Group 2 metal compounds (CAS version of the Periodic Table of the Elements). Examples include alkali metals such as sodium, potassium, lithium, copper, magnesium, calcium, barium, zinc, and cadmium. In one embodiment the metals are sodium, magnesium, or calcium.
  • the anionic portion of the basic metal compound can be hydroxide, oxide, carbonate, borate, or nitrate.
  • the metal-containing detergent contributes at least about 0.1 total base number, or at least 0.3 or 0.4 or 0.6 TBN to the lubricant composition, and in some embodiments up to 3 or 2 or 1 TBN.
  • the amount of the metal-containing detergent, if present, may in certain embodiments be up to 3 percent, e.g., 0.1 to 3 percent or 0.2 to 2 percent or 0. 25 to 1 percent or 0.3 to 0.6 percent by weight. In other embodiments, the metal-containing detergent may be present in an amount to deliver at least 0.01 percent sulfated ash to the composition.
  • the detergent may be present in an amount to deliver 0.01 to 0.12 percent sulfated ash or, alternatively, 0.05 to 0.1 percent, or even 0.06 to 0.09 percent.
  • the present lubricant is not an ash-free lubricant; that is, it may be an ash-containing detergent, containing 0.01 to 0.12 percent sulfated ash or, alternatively, 0.05 to 0.1 percent, or even 0.06 to 0.09 percent, which ash may be provided by the metal- containing detergent or detergents or in whole or in part from other sources such as zinc salts (e.g., zinc dialkyldithiophosphates), molybdenum compounds, or titanium compounds.
  • zinc salts e.g., zinc dialkyldithiophosphates
  • molybdenum compounds e.g., titanium compounds.
  • Another material which may be present in the lubricant is an antioxidant.
  • Antioxidants encompass phenolic antioxidants, which may be hindered phenolic antioxidants, one or both ortho positions on a phenolic ring being occupied by bulky groups such as t-butyl.
  • the para position may also be occupied by a hydrocarbyl group or a group bridging two aromatic rings.
  • the para position is occupied by an ester-containing group, such as, for example, an antioxidant of the formula
  • R is a hydrocarbyl group such as an alkyl group containing, e.g., 1 to 18 or 2 to 12 or 2 to 8 or 2 to 6 carbon atoms; and t-alkyl can be t-butyl.
  • alkyl group containing, e.g., 1 to 18 or 2 to 12 or 2 to 8 or 2 to 6 carbon atoms e.g., 1 to 18 or 2 to 12 or 2 to 8 or 2 to 6 carbon atoms
  • t-alkyl can be t-butyl.
  • Antioxidants also include aromatic amines.
  • an aromatic amine antioxidant can comprise an alkylated diphenylamine such as nonylated diphenyla- mine or a mixture of a di-nonylated and a mono-nonylated diphenylamine.
  • Antioxidants also include sulfurized olefins such as mono- or disulfides or mixtures thereof. These materials generally have sulfide linkages of 1 to 10 sulfur atoms, e.g., 1 to 4, or 1 or 2.
  • Materials which can be sulfurized to form the sulfurized organic compositions of the present invention include oils, fatty acids and esters, olefins and polyolefins made thereof, terpenes, or Diels-Alder adducts. Details of methods of preparing some such sulfurized materials can be found in U.S. Pat. Nos. 3,471,404 and 4,191,659.
  • Molybdenum compounds can also serve as antioxidants, and these materials can also serve in various other functions, such as antiwear agents or friction modifiers.
  • U.S. Pat. No. 4,285,822 discloses lubricating oil compositions containing a molybdenum- and sulfur-containing composition prepared by combining a polar solvent, an acidic molyb- denum compound and an oil-soluble basic nitrogen compound to form a molybdenum- containing complex and contacting the complex with carbon disulfide to form the molybdenum- and sulfur-containing composition.
  • Typical amounts of antioxidants will, of course, depend on the specific antioxidant and its individual effectiveness, but illustrative total amounts can be 0.005 to 5 percent by weight or 0.007 to 1 percent or 0.01 to 0.5 percent of 0.01 to 0.1 percent.
  • Yet another material that may optionally be present, or which may be absent, is a metal salt of a phosphorus acid.
  • R and R are independently hydrocarbyl groups containing 3 to 30 carbon atoms, are readily obtainable by heating phosphorus pentasulfide (P 2 S 5 ) and an alcohol or phenol to form an ⁇ , ⁇ -dihydrocarbyl phosphorodithioic acid.
  • P 2 S 5 phosphorus pentasulfide
  • the R and R groups may be a mixture of alcohols, for instance, a mixture of isopropanol and 4-methyl-2-pentanol, and in some embodiments a mixture of a secondary alcohol and a primary alcohol, such as isopropanol and 2-ethylhexanol.
  • the resulting acid may be reacted with a basic metal compound to form the salt.
  • the metal M having a valence n, generally is aluminum, tin, manganese, cobalt, nickel, zinc, or copper, and in many cases, zinc, to form zinc dialkyldithiophosphates ("ZDDP").
  • ZDDP zinc dialkyldithiophosphates
  • the lubricant formulation may be free from ZDDP or may contain only a low amount of one or more ZDDPs, such as to provide 0 to 0.05, or 0.001 to 0.02, or 0.001 to 0.005, or 0.005 to 0.01 weight percent phosphorus to the composition, and in one embodiment the lubricant formulation may contain the aforementioned amounts of phosphorus from all sources, total.
  • compositions of the present invention can be prepared by mixing the indicated components directly, or by preparing one or more of the components in the form of a concentrate, to which other components (such as oil or solvent) can subsequently be added.
  • the present lubricant may be supplied to an engine in any of a variety of ways, depending at least in part on the design of the engine. It may be supplied from a sump, in which case the optional volatile solvents will likely not be present. This arrangement would be more likely used in engines which are not designed to consume the lubricant in the combustion chamber. Many two-stroke cycle engines, however, are not sump- lubricated, and for them, the lubricant may be supplied along with the fuel, either by injection into the fuel stream or by premixing the lubricant into the bulk fuel.
  • the fuel into which the lubricant for a two-cycle engine is mixed is commonly, but not necessarily, gasoline.
  • Other possible liquid fuels included gasoline-alcohol mixtures ("gasohol") having 5%, 10%, or a larger percentage of ethanol, including 85% (“E- 85").
  • the lubricant may be blended into the liquid fuel in an amount or ratio of 1 :200 to 1 :25 by weight, or 1 :60 to 1 :40, or about 1 :50 (e.g., about 2% lubricant).
  • the lubricant of the present technology may be profitably employed in a two- stroke cycle engine.
  • Such engines are commonly used in lawn and garden equipment, portable contractor equipment such as pumps and electrical generators, low-cost transportation vehicles, such as mopeds, as well as commercial and recreational vehicles including motorcycles, outboard engines (for boats and marine vehicles), snowmobiles, and personal watercraft vehicles.
  • en- gines with a displacement of 2,000 to 3,000cm generate approximately 150 kW (201 hp).
  • 2-stroke cycle engines can also be found in very small applications, such as in power tools like weed trimmers or chain saws. These smaller engines typically output 1-5 kW and may have a cylinder displacement of 20 to 80cm .
  • the engines may have a power output of less than 150 kW, such as less than 100 or less than 50 or less than 20 kW; or 0.1 to 15 kW or 0.5 to 10 kW or 1-5 kW, and optionally a cylinder displacement of 10 to 300 cm 3 , or 15-100 or 20-80 cm 3 .
  • each chemical component described is presented exclusive of any solvent or diluent oil, which may be customarily present in the commercial material, that is, on an active chemical basis, unless otherwise indicated.
  • each chemical or composition referred to herein should be interpreted as being a commercial grade material which may contain the isomers, by-products, derivatives, and other such materials which are normally understood to be present in the commercial grade.
  • a series of lubricant compositions is tested in an SRM-265 two-stroke cycle string trimmer engine, 25.4 cm engine displacement.
  • the test is conducted for 50 hours or until engine seizure occurs, running the engine on a gasoline-lubricant mixture.
  • the test consists of two stages, a full throttle portion and an idle portion.
  • the engine is operated at the full throttle condition for 2 minutes and 15 seconds.
  • the engine is operated at the idle condition for 15 seconds. These two cycles are repeated for a total duration of 50 hours without interruption.
  • the engine is disassembled and inspected for varnish deposits and port blocking.
  • the lubricants and the piston skirt varnish ratings are reported in the table below.
  • ASTM merit scale ratings are used to evaluate engine parts with a rating of 10 representing a clean part and lower numbers representing more severe degrees of varnish down to the most severe which has a merit rating of 1.
  • c. product of polyisobutylene phenol, formaldehyde, and dimethylamine includes 10-11% heavy aromatic solvent.
  • the formulations below are subjected to a low temperature detergency test.
  • the test lubricant is used to lubricate a Husqvarna HVA 232 E-TechTM Scrub Cutter engine, a two-stroke cycle engine.
  • the carburetor H-needle is set to provide 3% CO at 8400 r.p.m., steady state conditions.
  • the test cycle comprises 2 seconds at full throttle followed by 3 seconds at idle, continuing for 36,000 cycles over 50 hours.
  • the only load is the inertia from the grass cutter.
  • the L-needle is set to give maximum 12,000 ( ⁇ 500) r.p.m. The lowest speed is normally around 6000 r.p.m.
  • cleanliness of various parts of the engine is measured. The results are shown in the table below. The maximum (best) rating for total cleanliness is 15.
  • c. product of polyisobutylene phenol, formaldehyde, and dimethylamine includes 10-11% heavy aromatic solvent.

Abstract

L'invention concerne une composition lubrifiante comprenant une huile de viscosité lubrifiante, 0,1 à 2 pour cent en poids d'un dispersant de Mannich et 0,1 à 2 pour cent en poids d'un dispersant succinimide, le dispersant succinimide fournissant au moins 40 parties par million en poids d'atomes d'azote à la composition lubrifiante, laquelle huile fournit une propreté à un moteur à deux temps.
PCT/US2012/044118 2011-07-07 2012-06-26 Lubrifiant fournissant une propreté améliorée pour des moteurs à deux temps WO2013006303A1 (fr)

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CA2841048A CA2841048A1 (fr) 2011-07-07 2012-06-26 Lubrifiant fournissant une proprete amelioree pour des moteurs a deux temps
JP2014518899A JP2014522893A (ja) 2011-07-07 2012-06-26 ２ストロークサイクルエンジンのための改善された清浄性を提供する潤滑剤
CN201280042936.XA CN103857775A (zh) 2011-07-07 2012-06-26 提供给二冲程发动机改善的清洁度的润滑剂
EP12735693.9A EP2729555A1 (fr) 2011-07-07 2012-06-26 Lubrifiant fournissant une propreté améliorée pour des moteurs à deux temps
US14/130,720 US20140130759A1 (en) 2011-07-07 2012-06-26 Lubricant Providing Improved Cleanliness For Two-Stroke Cycle Engines
IN114DEN2014 IN2014DN00114A (fr) 2011-07-07 2014-01-07

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US201161505172P 2011-07-07 2011-07-07
US61/505,172 2011-07-07

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EP3112447B1 (fr) * 2015-06-30 2018-03-28 Infineum International Limited Composition d'additif pour la lubrification d'un moteur marin
WO2017105747A1 (fr) * 2015-12-18 2017-06-22 The Lubrizol Corporation Polymères oléfiniques fonctionnalisés par un azote pour lubrifiants de moteur
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CN103857775A (zh) 2014-06-11
US20140130759A1 (en) 2014-05-15
CA2841048A1 (fr) 2013-01-10
IN2014DN00114A (fr) 2015-05-22
EP2729555A1 (fr) 2014-05-14
JP2014522893A (ja) 2014-09-08

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