WO2004101717A2 - High octane lubricants for knock mitigation in flame propagation engines - Google Patents
High octane lubricants for knock mitigation in flame propagation engines Download PDFInfo
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- WO2004101717A2 WO2004101717A2 PCT/US2004/014915 US2004014915W WO2004101717A2 WO 2004101717 A2 WO2004101717 A2 WO 2004101717A2 US 2004014915 W US2004014915 W US 2004014915W WO 2004101717 A2 WO2004101717 A2 WO 2004101717A2
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- lubricant composition
- manganese tricarbonyl
- base oil
- oil
- additives
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M171/00—Lubricating compositions characterised by purely physical criteria, e.g. containing as base-material, thickener or additive, ingredients which are characterised exclusively by their numerically specified physical properties, i.e. containing ingredients which are physically well-defined but for which the chemical nature is either unspecified or only very vaguely indicated
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- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
- C10M169/04—Mixtures of base-materials and additives
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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
- C10M2203/1006—Petroleum or coal fractions, e.g. tars, solvents, bitumen used as base material
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- 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
- C10M2205/0206—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers used as base material
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- 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
- C10M2205/028—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
- 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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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/021—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/04—Ethers; Acetals; Ortho-esters; Ortho-carbonates
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/281—Esters of (cyclo)aliphatic monocarboxylic acids
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
- C10M2207/2825—Esters of (cyclo)aliphatic oolycarboxylic acids used as base material
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- C10M2207/28—Esters
- C10M2207/283—Esters of polyhydroxy compounds
- C10M2207/2835—Esters of polyhydroxy compounds used as base material
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/102—Polyesters
- C10M2209/1023—Polyesters used as base material
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/08—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions having metal-to-carbon bonds
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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
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/08—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions having metal-to-carbon bonds
- C10M2227/081—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions having metal-to-carbon bonds with a metal carbon bond belonging to a ring, e.g. ferocene
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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
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/09—Complexes with metals
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/14—Group 7
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- 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
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
- C10N2020/015—Distillation range
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- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
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- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/255—Gasoline engines
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- 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
- C10N2070/00—Specific manufacturing methods for lubricant compositions
- C10N2070/02—Concentrating of additives
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02B—INTERNAL-COMBUSTION PISTON ENGINES; COMBUSTION ENGINES IN GENERAL
- F02B1/00—Engines characterised by fuel-air mixture compression
- F02B1/12—Engines characterised by fuel-air mixture compression with compression ignition
Definitions
- This invention pertains to lubricant oil compositions and processes that reduce the propensity for end gas knock in flame propagation engines.
- Engine knock is a phenomenon that occurs in a flame propagation engine due to auto ignition of a portion of the fuel air mixture ahead of the propagating flame front. This auto ignition occurs very rapidly; possibly creating a detonation wave that traverses the end gas leading to the audible ping or knock. This phenomena limits performance in all flame propagation engines because it limits the intake manifold pressure, the engine compression ratio, and the spark advance, factors that all affect the engine performance, emissions, and efficiency. There is much research directed toward reducing knock. Compositions of fuels and lubricants and methods to prevent or reduce such knock in flame propagation engines are highly desirable.
- Engine lube oil is intentionally coated on the cylinder line every stroke to reduce friction and to prevent ring and liner wear. Some of this lubricant enters the boundary layer of the cylinder and the combustion chamber in the end gas region.
- Typical lubricant base stocks have relatively high cetane number (and correspondingly low octane) or low auto-ignition temperatures.
- the boundary layer and the end gas region therefore consist of a mixture of fuel and air, at close to the air-fuel ratio of the main combustion chamber, and a relatively rich concentration of the lubricant. This means that the end gas auto-ignition temperature is lower, possibly significantly lower, than the fuel-air mixture in the middle of the combustion chamber.
- the present inventors have determined that a factor contributing to the early or undesirable onset of knock is the presence of lubricating oil in the end gas.
- Engine lubricating oil comprises base oil, which may be either petroleum (mineral) based or synthetic, and a number of additive components.
- the additive components include organometallics used for wear prevention, friction reduction, and acid neutralization, various viscosity modifiers, dispersants, and detergents.
- the auto ignition temperature of the base oils are typically much lower than the fuel in flame propagation engines, where the fuel can include gasoline, natural gas, LP gas, and hydrogen, to name a few. This means that the octane number of the base lubricant is very low, meaning that if the end gas contains any lubricant, either as droplets or vapor, the auto ignition temperature of the end gas can be very low and knock can occur.
- the base stock formulation and the additives affect both the propensity of the oil to enter the end gas as well as the auto ignition temperature of the oil.
- the inventors herein have found that lube oil can be flung into the high temperature fuel and air zone where the lubricant droplets easily auto-ignite, and this can create knock.
- the higher the acceleration of the engine the greater the amount of lubricant entering the fuel and air zone.
- the inventors have identified a number of factors that can be modified to reduce knock in the engine by for instance either limiting the amount of oil that enters the end gas region or by adjusting the octane number of the base oil and the fully formulated lubricant. These factors include, but are not limited to, the following: volatility of the lubricant, octane of the lubricant, viscosity of the lubricant, lube oil density, characteristics of the additive package (e.g., including additives for increasing the octane of the lubricant), and octane characteristics of the base stock.
- a decrease of the lubricant's volatility and/or increasing the viscosity will result in less low octane lubricant droplets entering the end gas and thus lessen the octane reduction in the end gas then would otherwise result from the lubricant if it had a higher volatility and/or lower viscosity.
- the volatility of the lubricant can be modified by, for example, increasing the average boiling point of the base oil, or by the use of a narrower boiling range.
- the viscosity can be modified in a similar way, and/or by adding an additive to increase viscosity.
- by modifying the density of the lubricant one can affect the amount of lubricant that enters the end gas. Higher density lubricant will have less propensity to enter the end gas; thus, by employing higher density base oil, one can increase the density and thereby decrease the amount of low octane lubricant that enters the end gas, whereby the lubricant has less propensity to contribute to end gas knock.
- the propensity of end gas knock can also be affected by modifying the octane of the lubricant to above 80, by employing a lubricant formulation that has an elevated pressure auto ignition temperature ("EPAIT") of at least 500 K, and/or by employing a lubricant composition that has an average boiling point in excess of 200 °C.
- EPAIT elevated pressure auto ignition temperature
- octane number are somewhat inter-related such that an increase of a lubricant's EPAIT usually also increases the octane number.
- the lubricant composition which may comprise base oil and one or more additives, has an EPAIT of at least about 500 K.
- EPAIT may be measured by using a constant volume combustion bomb (an "IQT" device, which has been used previously to measure auto ignition characteristics such as the cetane number of diesel fuels) to determine the ignition delay time as a function of the initial air temperature in the IQT, such as described in "Fuel Requirements for HCC1 Engine Operation,” by Thomas W. Ryan III and Andrew C. Matheaus, which published as paper SAE 2003-01-1813 at the JSAE/SAE International Spring Fuels & Lubricants Meeting, Yokohama, Japan, May 19-22, 2003.
- IQT constant volume combustion bomb
- the ignition delay time-temperature relationship consistently shows an Arrhenius type of relationship.
- This relationship can be used to define the ignition temperature at any ignition delay time. This allows one to select an ignition delay time (e.g., 7 milliseconds) that would then be used to determine the temperature at which ignition occurred for a given fuel, i.e., to define the EPAIT.
- the EPAIT can be raised to above 500 K (in one embodiment above 600 K) by increasing the EPAIT of the base oil such as by changing the composition of the base oil in question or by adding one or more EPAIT modifying additives to the base oil.
- the lubricant composition which may comprise a base oil and one or more additives, has an octane number ((R+M)/2) of at least about 80. In one embodiment, the octane number is at least about 85. Octane can be measured using well known procedures. If the lubricant composition has an octane number below about 80, it can be increased in a number of ways, such as by raising the octane number of the base oil or by adding one or more additives that increases the octane of the composition. Representative examples of such additives include tetra ethyl lead and other organometallics such as "MMT.” MMT is a commercially available octane improver additive for engine fuels.
- this invention is a lubricant composition for reducing the propensity of end gas knock in a flame propagation engine, comprising: a base oil and one or more additives, where the composition has (a) an octane number of at least about 80, (b) an elevated pressure auto ignition temperature of at least about 500 K, or (c) both (a) and (b).
- this invention is a process for reducing the propensity for end gas knock in a flame propagation engine, comprising: using a lubricant composition as the engine oil wherein the lubricant composition comprises a base oil and one or more additives, where the composition has (a) an octane number of at least about 80, (b) an elevated pressure auto ignition temperature of at least about 500 K, or (c) both (a) and (b).
- this invention is a process for manufacturing a lubricant composition that reduces the propensity for engine knock in a flame propagation engine, comprising: formulating a lubricant composition which comprises a base oil and one or more additives wherein the lubricant composition has (a) an octane number of at least about 80, (b) an elevated pressure auto ignition temperature of at least about 500 K, or (c) both (a) and (b).
- this invention is a method for identifying a lubricant composition that reduce the propensity for end gas knock in a flame propagation engine, comprising: subjecting a sample of a lubricant composition to (a) an elevated pressure auto ignition temperature test to determine whether the sample has an elevated pressure auto ignition temperature of at least about 500 K, (b) an octane number test to determine whether the sample as an octane number of at least about 80, or (c) both (a) and (b).
- the lubricant may comprise a base oil and one or more additives.
- This method may include the step of adding an octane- improver additive to increase the elevated pressure auto ignition temperature of the lubricant composition to at least about 500 K and/or octane number of the lubricant composition to at least about 80, and optionally including the step of subjecting the lubricant composition that contains the octane-increase additive to (a), (b), or (c).
- the lubricant composition which may comprise a base oil and one or more additives, has an average boiling point in excess of 200 °C.
- this invention is a lubricant composition for reducing the propensity of end gas knock in a flame propagation engine, comprising: a base oil and one or more additives, wherein the composition has an average boiling point in excess of 200 °C.
- this invention is a process for reducing the propensity for end gas knock in a flame propagation engine, comprising: using a lubricant composition as the 1 engine oil wherein the lubricant composition comprises a base oil and one or more additives,
- composition has a average boiling point in excess of 200 °C. 3
- this invention is a process for manufacturing a lubricant
- a lubricant composition which comprises a base oil and one or more
- this invention is a method for identifying a lubricant
- This method may include the step
- the base oil can be a natural oil; the base oil can be derived
- the base oil can be a mineral oil; the base oil can be a synthetic oil; the base
- the 20 oil can be a polyalphaolefin oil; the base oil can be a polyester oil; the one or more additives can
- 21 include at least one of an alcohol, an ether, an ester, an organometallic compound, or
- the one or more additives can include at least one of ferrocene, butyl
- the one or more additives can include at least one of ethyl
- 25 isobutyl alcohol, methyl butyrate, methyl caproate, methyl caprylate, or combination thereof;
- one or more additives can include at least one of cyclopentadienyl manganese tricarbonyl,
- the base oil can be present in the lubricant composition in an amount of from about 0.01% to about 99% by weight.; the base oil can be present in the lubricant composition in an amount of from about 0.1% to about 80% by weight; the one or more additives can be present in an amount of from about 0.01% to about 20% by weight; the one or more additives can be present in an amount of from about 0.1% to about 10% by weight; or any combination thereof.
- the present invention has a number of advantages, including the ability to reduce the propensity of end gas knock in a flame propagation engine, without having to modify the engine fuel that is sent to the engine from the fuel tank.
- Unrefined, refined and rerefined oils can be used as the base oils in the lubricants of the present invention.
- Unrefined oils are those obtained directly from a natural or synthetic source without further purification treatment.
- a shale oil obtained directly from retorting operations a petroleum oil obtained directly from primary distillation or ester oil obtained directly from an esterification process and used without further treatment would be an unrefined oil.
- 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.
- oils are obtained by processes similar to those used to obtain refined oils applied to refined oils which have been already used in service. Such rerefined oils are also known as reclaimed or reprocessed oils and often are additionally processed by techniques directed to removal of spent additives and oil breakdown products. Likewise, the oils may be made using a Fisher-Tropsch process.
- Oils of lubricating viscosity derived from coal or shale are useful in the practice of this invention.
- Mineral oils are useful as the base oil in the practice of this invention.
- Mineral oils include petroleum oils, and treated petroleum oils.
- the mineral oils may be a paraffinic, naphthenic and/or aromatic types.
- Specific mineral oils include hydrotreated mineral oils, solvent refined mineral oils, isomerized wax oils, solvent refined and acid treated mineral oils, etc., wax basestocks, and 120 N isomerized wax basestocks.
- the lubricating compositions of this invention employ an oil of lubricating viscosity, including natural or synthetic lubricating oils and mixtures thereof.
- oils include mineral oil and synthetic oils, such as polyalphaolefin oils and polyester oils, may be used.
- Synthetic lubricating oils include hydrocarbon oils and halosubstituted hydrocarbon oils such as polymerized and interpolymerized olefins, etc.
- alkylbenzenes polyphenyl, (e.g., biphenyls, terphenyls, alkylated polyphenyls, etc.), alkylated diphenyl ethers and alkylated diphenyl sulfides and their derivatives, analogs and homologues thereof and the like.
- Alkylene oxide polymers and inte olymers and derivatives thereof, and those where terminal hydroxyl groups have been modified by esterification, etherification, etc. constitute other classes of known synthetic lubricating oils that can be used.
- Another suitable class of synthetic lubricating oils that can be used comprises the esters of dicarboxylic acids and those made from C5 to C12 monocarboxylic acids and polyols or polyether polyols.
- Other synthetic lubricating oils include liquid esters of phosphorus-containing acids, polymeric tetrahydrofurans, alkylated diphenyloxides and the like.
- Natural oils useful in making the inventive lubricants and functional fluids include animal oils and vegetable oils (e.g., lard oil, castor oil) 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 which may be further refined by hydrocracking and hydrofinishing processes and are dewaxed. Oils of lubricating viscosity derived from coal or shale are also useful.
- animal oils and vegetable oils e.g., lard oil, 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 which may be further refined by hydrocracking and hydrofinishing processes and are dewaxed. Oils of lubricating viscosity derived from coal or shale are also useful.
- Synthetic lubricating oils include hydrocarbon oils and halo-substituted hydrocarbon oils such as polymerized and interpolymerized olefins (e.g., polybutylenes, polypropylenes, propylene-isobutylene copolymers, chlorinated polybutylenes, etc.); poly(l- hexenes), poly-(l-octenes), poly(l-decenes), etc.
- alkyl-benzenes e.g., dodecylbenzenes, tetradecylbenzenes, dinonylbenzenes, di-(2-ethylhexyl)-benzenes, etc.
- polyphenyls e.g., biphenyls, terphenyls, alkylated polyphenyls, etc.
- Alkylene oxide polymers and interpolymers and derivatives thereof where the terminal hydroxyl groups have been modified by esterification, etherification, etc. constitute another class of known synthetic lubricating oils that can be used. These are exemplified by the oils prepared through polymerization of ethylene oxide or propylene oxide, the alkyl and aryl ethers of these polyoxyalkylene polymers (e.g., methyl-polyisopropylene glycol ether having an average molecular weight of about 1000, diphenyl ether of polyethylene glycol having a molecular weight of about 500-1000, diethyl ether of polypropylene glycol having a molecular weight of about 1000-1500, etc.) or mono- and polycarboxylic esters thereof, for example, the acetic acid esters, mixed C3-C8 fatty acid esters, or the C13 oxo acid diester of tetraethylene glycol.
- Another suitable class of synthetic lubricating oils that can be used comprises the esters of dicarboxylic acid (e.g., phthalic acid, succinic acid, alkyl succinic acids, alkenyl succinic acids, maleic acid, azelaic acid, suberic acid, sebacic acid, furmaric acid, adipic acid, linoleic acid dimer, malonic acid, alkyl malonic acids, alkenyl malonic acids, etc.) with a variety of alcohols (e.g., butyl alcohol, hexyl alcohol, dodecyl alcohol, 2-ethylhexyl alcohol, ethylene glycol, diethylene glycol monoether, propylene glycol, etc.).
- dicarboxylic acid e.g., phthalic acid, succinic acid, alkyl succinic acids, alkenyl succinic acids, maleic acid, azelaic acid, suberic acid, sebacic acid, furmaric acid,
- esters include dibutyl adipate, di(2-ethylhexyl) sebacate, di-n-hexyl fumarate, dioctyl sebacate, diisooctyl azelate, diisodecyl azelate, dioctyl phthalate, didecyl phthalate, dieicosyl sebacate, the 2-ethylhexyl diester of linoleic acid dimer, the complex ester formed by reacting one mole of sebacid acid with two moles of tetraethylene glycol and two moles of 2-ethylhexanoic acid and the like.
- Esters useful as synthetic oils also include those made from C5 to C12 monocarboxylic acids and polyols and polyol ethers such as neopentyl glycol, trimethylol propane, pentaerythritol, dipentaerythritol, tripentaerythritol, etc.
- Silicon-based oils such as the polyalkyl-, polyaryl-, polyalkoxy-, or polyaryloxy-siloxane oils and silicate oils comprise another useful class of synthetic lubricants (e.g., tetraethyl silicate, tetraisopropyl silicate, tetra-(2-ethlhexyl)silicate, tetra-(4-methyl-hexyisilicate, tetra-(p-tert- butylphenyl) silicate, hexyl-(4-methyl-2-pentoxy)disiloxane, poly(methyl) siloxanes, poly- (methylphenyl siloxanes, etc.).
- synthetic lubricants e.g., tetraethyl silicate, tetraisopropyl silicate, tetra-(2-ethlhexyl)silicate, tetra-(4-methyl-hexyisilicate
- compositions of this invention contain from about 0.01% to about 99% by weight of the base oil.
- the base oil can be present in the lubricant composition in an amount of from about 0.1% to about 90% by weight, and in another embodiment up to about 80% base oil.
- Lubricating oil compositions of this invention contain additives.
- the selection of such additives will depend on the particular use. Any given additive may be included or excluded.
- Octane improvement additives can be employed in the practice of this invention. Additives that can be used as an octane booster include, but are not limited to, alcohols, ethers, esters, and organometallic compounds. Other known octane boosters also may be used. These additives can be used alone or together with others. Octane boosting and other additives may be present in the range of a few ppm to about 50% by weight.
- non- organometallic octane boosters are ethyl acetate, isoamyl acetate, amyl acetate, isoamyl propionate, isoamyl nonanoate, isobutyl acetate, isobutyl alcohol, methyl butyrate, methyl caproate, and methyl caprylate.
- organometallic compound refers to a metal-containing compound whose molecules include carbon-metal linkage.
- Suitable organometallic compounds include any such compounds which are known to those of skill in the art to increase the octane rating of fuels such as tetra ethyl lead and methylcyclopentadienyl manganese tricarbonyl (MMT), which are used in the practice of this invention to increase octane of the lubricant composition.
- MMT methylcyclopentadienyl manganese tricarbonyl
- organo- manganese compounds and organo-iron compounds are especially suitable.
- Other metals may include, but are not limited to, metals of Groups IB, IIB, IIIB, IVB, VB, VIB, VIIB, and VIIIB of the Periodic Table of the Elements.
- ferrocene and butyl ferrocene are used as octane boosters.
- an organometallic such as methylcyclopentadienyl manganese tricarbonyl ("MMT") is used as an octane booster.
- MMT methylcyclopentadienyl manganese tricarbonyl
- metallocene compounds are such organometallic compounds.
- cyclopentadienyl manganese compounds useful in the method and compositions of his invention have the general formula: Mn A (B) 3 wherein A represents cyclomatic radical containing from 5 to 13 carbon atoms and B is a carbonyl.
- the constituent designated by the symbol A in the formula comprises a cyclomatic radical, that is, a cyclopentadiene-type hydrocarbon radical which is a radical containing the cyclopentadienyl moiety.
- a cyclomatic radical that is, a cyclopentadiene-type hydrocarbon radical which is a radical containing the cyclopentadienyl moiety.
- cyclomatic hydrocarbon groups contain 4 to 20 carbons, in one embodiment from 5 to 13 carbon atoms.
- radicals are cyclopentadienyl, indenyl, methylcyclopentadienyl, propylcyclopentadienyl, diethylcyclopentadienyl, phenylcyclopentadienyl, tert-butylcyclopentadienyl, p-ethylphenylcyclopentadienyl, 4-tert-butyl indenyl and the like.
- Representative compounds include cyclopentadienyl manganese tricarbonyl, methylcyclopentadienyl manganese tricarbonyl, ethylcyclopentadienyl manganese tricarbonyl, propylcyclopentadienyl manganese tricarbonyl, indenyl manganese tricarbonyl, methyl indenyl manganese tricarbonyl, fluorenyl manganese tricarbonyl, dimethylcyclopentadienyl manganese tricarbonyl, methylpropylcyclopentadienyl manganese tricarbonyl, phenylcyclopentadienyl manganese tricarbonyl and the like.
- Lubricant compositions often comprise a zinc salt of a dithiophosphoric acid.
- Zinc salts of dithiophosphoric acids are often referred to as zinc dithiophosphates, zinc O,O-dihydrocarbyl dithiophosphates, and other commonly used names. They are sometimes referred to by the abbreviation ZDP.
- ZDP zinc dithiophosphates
- One or more zinc salts of dithiophosphoric acids may be present in a minor amount to provide additional extreme pressure, anti-wear and anti-oxidancy performance.
- additives that may optionally be used in the lubricating oils of this invention include, for example, detergents, dispersants, supplemental viscosity improvers, oxidation inhibiting agents, corrosion inhibiting agents, pour point depressing agents, extreme pressure agents, anti-wear agents, color stabilizers and anti-foam agents.
- detergents for example, detergents, dispersants, supplemental viscosity improvers, oxidation inhibiting agents, corrosion inhibiting agents, pour point depressing agents, extreme pressure agents, anti-wear agents, color stabilizers and anti-foam agents.
- dispersants and supplemental viscosity improvers may be used in addition to the nitrogen containing esters of this invention.
- Extreme pressure agents and corrosion and oxidation inhibiting agents which may be included in the compositions of the invention are exemplified by chlorinated aliphatic hydrocarbons, organic sulfides and polysulfides, phosphorus esters including dihydrocarbon and trihydrocarbon phosphites, molybdenum compounds, and the like.
- oxidation inhibiting agents include materials such as alkylated diphenyl amines, hindered phenols, especially those having tertiary alkyl groups such as tertiary butyl groups in the position ortho to the phenolic —OH group, and others.
- Viscosity improvers are usually polymers, including polyisobutenes, polymethacrylic acid esters, hydrogenated diene polymers, polyalkyl styrenes, esterified styrene-maleic anhydride copolymers, hydrogenated alkenylarene-conjugated diene copolymers and polyolefms.
- Multifunctional viscosity improvers other than those of the present invention, which also have dispersant and/or antioxidancy properties are known and may optionally be used in the practice of this invention.
- Pour point depressants may be included in the additive concentrates and lubricating oils described herein. Those which may be used are described in the literature and are well-known.
- Anti-foam agents used to reduce or prevent the formation of stable foam include silicones or organic polymers.
- Detergents and dispersants may be of the ash-producing or ashless type.
- the ash- producing detergents are exemplified by oil soluble neutral and basic salts of alkali or alkaline earth metals with sulfonic acids, carboxylic acids, phenols or organic phosphorus acids characterized by a least one direct carbon-to-phosphorus linkage.
- Ashless detergents and dispersants are so-called despite the fact that, depending on its constitution, the detergent or dispersant may upon combustion yield a nonvolatile residue such as boric oxide or phosphorus pentoxide; however, it does not ordinarily contain metal and therefore does not yield a metal- containing ash on combustion.
- Many types are known in the art, and any of them are suitable for use in the lubricants of this invention. The following are illustrative:
- additives may each be present in lubricating compositions at a concentration of as little as 0.001% by weight, usually ranging from about 0.01% to about 20% by weight. In most instances, they each contribute from about 0.1% to about 10% by weight, more often up to about 5% by weight.
- Additive Concentrates may each be present in lubricating compositions at a concentration of as little as 0.001% by weight, usually ranging from about 0.01% to about 20% by weight. In most instances, they each contribute from about 0.1% to about 10% by weight, more often up to about 5% by weight.
- the various additives described herein can be added directly to the base oil or lubricant composition.
- the additives may be diluted with a substantially inert, normally liquid organic diluent such as mineral oil, naphtha, benzene, toluene or xylene, to form an additive concentrate.
- a substantially inert, normally liquid organic diluent such as mineral oil, naphtha, benzene, toluene or xylene
- These concentrates usually comprise about 0.1 to about 80% by weight, frequently from about 1% to about 80% by weight, more often from about 10% to about 80% by weight, of the compositions of this invention and may contain, in addition, one or more other additives known in the art or described hereinabove. Concentrations such as 15%, 20%, 30% or 50% or higher may be employed.
- Additive concentrates are prepared by mixing together the desired components, often at elevated temperatures, usually less than 100 C, often no more than about 70 C. .
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Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006533004A JP2007517921A (en) | 2003-05-12 | 2004-05-12 | High octane lubricant for knock mitigation in flame propagation engines |
GB0511605A GB2427410A (en) | 2003-05-12 | 2004-05-12 | High octane lubricants for knock mitigation in flame propagation engines |
EP04752045A EP1625191A4 (en) | 2003-05-12 | 2004-05-12 | High octane lubricants for knock mitigation in flame propagation engines |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US46976903P | 2003-05-12 | 2003-05-12 | |
US60/469,769 | 2003-05-12 |
Publications (2)
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WO2004101717A2 true WO2004101717A2 (en) | 2004-11-25 |
WO2004101717A3 WO2004101717A3 (en) | 2008-06-12 |
Family
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Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2004/014915 WO2004101717A2 (en) | 2003-05-12 | 2004-05-12 | High octane lubricants for knock mitigation in flame propagation engines |
Country Status (6)
Country | Link |
---|---|
US (1) | US7262155B2 (en) |
EP (1) | EP1625191A4 (en) |
JP (1) | JP2007517921A (en) |
GB (1) | GB2427410A (en) |
SA (1) | SA04250116B1 (en) |
WO (1) | WO2004101717A2 (en) |
Cited By (6)
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WO2015023559A1 (en) * | 2013-08-12 | 2015-02-19 | Shell Oil Company | Methods for modifying auto-ignition properties of a base oil or lubricant composition |
WO2016012491A1 (en) | 2014-07-24 | 2016-01-28 | Total Marketing Services | Lubricating composition comprising an anti-knock compound |
WO2016135036A1 (en) | 2015-02-27 | 2016-09-01 | Shell Internationale Research Maatschappij B.V. | Use of a lubricating composition |
WO2016191409A1 (en) * | 2015-05-28 | 2016-12-01 | Exxonmobil Research And Engineering Company | Composition and method for preventing or reducing engine knock and pre-ignition in high compression spark ignition engines |
WO2019112711A1 (en) * | 2017-12-04 | 2019-06-13 | Exxonmobil Research And Enginerring Company | Method for preventing or reducing low speed pre-ignition |
WO2023057581A1 (en) | 2021-10-07 | 2023-04-13 | Totalenergies Onetech | Lubricating composition for preventing or reducing abnormal combustion in an engine |
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US20090286705A1 (en) * | 2008-04-10 | 2009-11-19 | Marc-Andre Poirier | Flame retardant lubricating oil compositions |
US8129320B2 (en) * | 2009-09-10 | 2012-03-06 | Southwest Research Institute | Lubricant oil compositions to optimize internal combustion engine performance |
US8026105B1 (en) | 2010-04-06 | 2011-09-27 | Southwest Research Institute | Quantification of lubricant reactivity using constant volume combustion device |
DE102010056514A1 (en) * | 2010-12-31 | 2012-07-05 | Fev Gmbh | Method for reduction of nitrogen oxide emission in diesel engine of motor car, involves providing parts of exhaust gas to form residue exhaust gas in chamber, and adjusting residue gas and/or ratio between parts of gas in chamber |
US20140165942A1 (en) | 2012-12-18 | 2014-06-19 | Ford Global Technologies, Llc | Engine-lubricant octane boost to quiet sporadic pre-ignition |
FR3020377B1 (en) * | 2014-04-25 | 2020-11-27 | Total Marketing Services | LUBRICATING COMPOSITION INCLUDING AN ANTI-CLICKING COMPOUND |
US9896634B2 (en) | 2014-05-08 | 2018-02-20 | Exxonmobil Research And Engineering Company | Method for preventing or reducing engine knock and pre-ignition |
US9944877B2 (en) | 2014-09-17 | 2018-04-17 | Exxonmobil Research And Engineering Company | Composition and method for preventing or reducing engine knock and pre-ignition in high compression spark ignition engines |
CN104762125B (en) * | 2015-02-10 | 2018-02-13 | 山东源根石油化工有限公司 | A kind of engine lubricating oil |
JP6502149B2 (en) * | 2015-04-06 | 2019-04-17 | Emgルブリカンツ合同会社 | Lubricating oil composition |
CN108026474B (en) * | 2015-09-28 | 2021-07-27 | Jxtg能源株式会社 | Cylinder lubricating oil composition for crosshead diesel engine |
WO2019224647A1 (en) * | 2018-05-25 | 2019-11-28 | Chevron U.S.A. Inc. | Method for preventing or reducing low speed pre-ignition in direct injected spark-ignited engines with manganese-containing lubricant |
CN111979015B (en) * | 2020-09-03 | 2022-09-16 | 天津大学 | Lubricating oil capable of hardening cylinder wall in combustion process, preparation method and application |
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- 2004-05-12 GB GB0511605A patent/GB2427410A/en not_active Withdrawn
- 2004-05-12 WO PCT/US2004/014915 patent/WO2004101717A2/en active Application Filing
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Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2015023559A1 (en) * | 2013-08-12 | 2015-02-19 | Shell Oil Company | Methods for modifying auto-ignition properties of a base oil or lubricant composition |
WO2016012491A1 (en) | 2014-07-24 | 2016-01-28 | Total Marketing Services | Lubricating composition comprising an anti-knock compound |
WO2016135036A1 (en) | 2015-02-27 | 2016-09-01 | Shell Internationale Research Maatschappij B.V. | Use of a lubricating composition |
WO2016191409A1 (en) * | 2015-05-28 | 2016-12-01 | Exxonmobil Research And Engineering Company | Composition and method for preventing or reducing engine knock and pre-ignition in high compression spark ignition engines |
US10119093B2 (en) | 2015-05-28 | 2018-11-06 | Exxonmobil Research And Engineering Company | Composition and method for preventing or reducing engine knock and pre-ignition in high compression spark ignition engines |
WO2019112711A1 (en) * | 2017-12-04 | 2019-06-13 | Exxonmobil Research And Enginerring Company | Method for preventing or reducing low speed pre-ignition |
WO2023057581A1 (en) | 2021-10-07 | 2023-04-13 | Totalenergies Onetech | Lubricating composition for preventing or reducing abnormal combustion in an engine |
FR3127954A1 (en) | 2021-10-07 | 2023-04-14 | Totalenergies Marketing Services | Lubricating composition for preventing or reducing abnormal combustion in an engine |
Also Published As
Publication number | Publication date |
---|---|
JP2007517921A (en) | 2007-07-05 |
GB2427410A (en) | 2006-12-27 |
US7262155B2 (en) | 2007-08-28 |
WO2004101717A3 (en) | 2008-06-12 |
GB0511605D0 (en) | 2005-07-13 |
EP1625191A4 (en) | 2011-02-16 |
EP1625191A2 (en) | 2006-02-15 |
SA04250116B1 (en) | 2008-03-30 |
US20040242436A1 (en) | 2004-12-02 |
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