WO2006105025A1 - Solid additive composition and method thereof - Google Patents
Solid additive composition and method thereof Download PDFInfo
- Publication number
- WO2006105025A1 WO2006105025A1 PCT/US2006/011121 US2006011121W WO2006105025A1 WO 2006105025 A1 WO2006105025 A1 WO 2006105025A1 US 2006011121 W US2006011121 W US 2006011121W WO 2006105025 A1 WO2006105025 A1 WO 2006105025A1
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- agents
- additive composition
- component
- mixture
- additive
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- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2215/042—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
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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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
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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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/08—Amides
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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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/08—Amides
- C10M2215/082—Amides containing hydroxyl groups; Alkoxylated derivatives
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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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/22—Heterocyclic nitrogen compounds
- C10M2215/225—Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
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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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/26—Amines
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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
- 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
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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
- 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
- C10M2217/044—Polyamides
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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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
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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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/08—Hydraulic fluids, e.g. brake-fluids
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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
- 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
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/08—Solids
Definitions
- the present invention relates to a solid additive composition comprising an additive and a solid matrix material.
- the invention further relates to a method to enhance performance of a functional fluid comprising adding the solid additive composition to a functional fluid, such as a fuel composition or a power transmission fluid.
- supplemental or additional additives into a functional fluid in a convenient manner such as a solid additive composition to enhance the performance of the functional fluid.
- the enhancement in performance can be a) maintaining the performance under harsh operating conditions, b) a further improvement in performance under normal operating conditions, c) an extension of performance beyond the normal life of the fluid, d) a restoration of performance, e) combinations thereof.
- Jakob et al. in US Patent No. 6,312,480 disclose a solid fuel additive.
- Schuettenberg et al. in US Patent Nos. 4,515,740 and 4,639,255 disclose solid form additives and a method of forming them.
- the present invention provides a solid additive composition in a form that allows for a convenient and effective enhancement in performance of a functional fluid, and in one embodiment preferably a hydrocarbon fuel composition or a power transmission fluid.
- An object of the present invention is to enhance the performance of a functional fluid effectively and in a convenient way.
- An additional object of this invention is to enhance the performance of a hydrocarbon fuel composition.
- a further object of the invention is to enhance the performance of a power transmission fluid.
- an additive composition comprises
- an additive comprising a fuel or lubricant additive selected from the group comprising antioxidants, extreme pressure agents, wear reduction agents, viscosity index improvers, anti-foaming agents, combustion modifiers, friction reducing agents, extreme pressure (EP) agents, wear reduction agents, viscosity index improvers, anti-foaming agents, anti-misting agents, cloud-point depressants, pour-point depressants, mineral or synthetic oils, anti-knock agents, lead scavengers, dyes, cetane improvers, rust inhibitors, bacteriostatic agents, gum inhibitors, fluidizers, metal deactivators, demulsifiers, anti-icing agents, lubricity additives, friction modifiers, viscosity improvers, flow improvers, low temperature improvers, anti-static agents, valve-seat recession agents, intake valve deposit control additives, combustion chamber deposit control additives, fuel injector deposit control additives, a fuel-borne catalysts (organometallic compounds of e.g, titanium
- component (B) at least one solid organic matrix material wherein the additive composition is a solid that melts in the range of about 25 to about 200 0 C, and each of component (A) and component (B) is present in the additive composition at about 5 to about 95% by weight.
- a nitrogen-containing detergent comprising at least one component selected from (a) a Mannich detergent prepared from the reaction of a hydrocarbyl- substituted hydroxy-containing aromatic compound and an aldehyde and an amine having at least one primary or secondary amino group; (b) a polyetheramine prepared from the reaction of an alkoxylated alcohol or an alkoxylated alkylphenol with acrylonitrile to form a nitrile which is hydrogenated to form the polyetheramine; (c) an alkoxylated reaction product of the reaction product of a C6- 36 aliphatic or aromatic carboxylic acid and polyethylenepolyamines; (d) a C6-36 aliphatic or aromatic amine or (e) a mixture thereof;
- a fatty acid derived friction modifier comprising of (a) a polyalkoxylated fatty amine; (b) a fatty acid derived oxazoline; and (c) a mixture thereof; or
- additive composition at least one solid organic matrix material wherein the additive composition is a solid that melts in the range of about 25 to about 200 0 C, and each of component (A) and component (B) is present in the additive composition in the range of about 5 to about 95% by weight of the additive composition.
- a method to enhance the performance of a functional fluid comprises adding a performance enhancing amount of the additive composition to the functional fluid.
- the present invention comprises an additive composition
- an additive composition comprising (A) an additive comprising (1) a nitrogen-containing detergent comprising (a) a Mannich detergent prepared from the reaction of a hydrocarbyl-substituted hydroxy- containing aromatic compound and an aldehyde and an amine having at least one primary or secondary amino group; (b) a polyetheramine prepared from the reaction of an alkoxylated alcohol or an alkoxylated alkylphenol with acrylonitrile to form a nitrile which is hydrogenated to form the polyetheramine; (c) an alkoxylated reaction product of the reaction product of a fatty carboxylic acid and naphthenic acid and polyethylenepolyamines; and (d) a mixture thereof; (2) a fatty acid derived friction modifier comprising (a) a polyalkoxylated fatty amine; (b) a fatty acid derived oxazoline; and (c) a mixture thereof; or (3) a mixture thereof; and (B) at least one solid
- the additive (A) of the present invention comprises (A)(I) a nitrogen- containing detergent, (A)(2) a fatty acid derived friction modifier, or (A)(3) a mixture thereof.
- Additive (A) can be a mixture comprising 2 or more detergents, 2 or more friction modifiers, 1 or more detergents and 1 or more friction modifiers or combinations thereof.
- the nitrogen-containing detergent of the invention can be (A)(l)(a) a Mannich detergent from the reaction of a hydrocarbyl-substituted hydroxy- containing aromatic compound and an aldehyde and an amine having at least one primary or secondary amino group.
- a hydrocarbyl group throughout this application is defined as a univalent group predominately hydrocarbon in nature that can have heteroatoms such as nitrogen and oxygen in the main chain of the hydrocarbon or attached to the main chain as a separate atom such as a halogen atom or in a group such as a hydroxy group.
- the hydrocarbyl substituent of the Mannich detergent can be derived from a polyolefm.
- the polyolefin can be a polymer of a C 2 -C 10 alkene or a mixture thereof.
- the hydrocarbyl substituent can have a number average molecular weight of about 200 to about 5,000; about 300 to about 3,000; about 400 to about 2,500; or about 900 to about 1,500.
- the hydrocarbyl substituent can be derived from a polyisobutylene or a polyisobutylene having a terminal double bond isomer content or vinylidene content of greater than about 50%, greater than about 60%, or greater than about 70%.
- the hydroxy-containing aromatic compound can have 1 or more hydroxy groups, none to 1 or more Ci-C 8 alkyl groups, or a mixture thereof to include for example phenol, catechol, and o-cresol.
- the aldehyde can have 1 to 6 carbon atoms to include formaldehyde in its reactive forms such as formalin and paraformaldehyde.
- the amine can be a monoamine, a polyamine, or a mixture thereof.
- the monoamine can be a primary monoamine, a secondary monoamine, an alkanolamine, or a mixture thereof.
- the monoamine can be for example a butylamine, dimethylamine, or ethanolamine.
- the polyamine can be an alkylenediamine or substituted derivative thereof such as ethylenediamine, a polyethylenepolyamine such as diethylenetriamine, an alkanolamine such as 2-(2- aminoethylamino)ethanol, or a mixture thereof.
- the preparation of Mannich detergents is known to those skilled in the art, and an illustrative preparative procedure is described in US Patent No. 5,876,468.
- the nitrogen-containing detergent of the invention can be (A)(l)(b) a polyetheramine prepared from the reaction of an alkoxylated alcohol or an alkoxylated alkylphenol with acrylonitrile to form a nitrile which is hydrogenated to form the polyetheramine.
- the alcohol can be an aliphatic alcohol, aromatic alcohol, or a mixture thereof.
- the aliphatic alcohol can have a branched carbon chain, a straight carbon chain, or a mixture thereof.
- the aliphatic alcohol can have about 1 to about 30,. about 4 to about 24, or about 8 to about 20 carbon atoms.
- the aliphatic alcohol can be a mixture of about 2 or more alcohols where each alcohol has a different number of carbon atoms.
- the alkyl substituent of the alkylphenol can have about 1 to about 30, about 2 to about 24, or about 4 to about 18 carbon atoms.
- the alkoxylated alcohol or alkylphenol can be prepared by reacting the alcohol or alkylphenol with 1 or more units of an alkylene oxide per unit of alcohol or alkylphenol generally in a based catalyzed condensation.
- the alkylene oxide can be a single alkylene oxide or a mixture of about 2 or more alkylene oxides differing in carbon number. The mixture of alkylene oxides can be reacted with the alcohol or alkylphenol in a combination or sequentially.
- the alkylene oxide can have about 2 to about 18, about 2 to about 10, about 2 to about 4, or about 3 to about 4 carbon atoms.
- the alkylene oxide can be ethylene oxide, propylene oxide, butylene oxide, or a mixture thereof.
- the number of moles of alkylene oxide reacted per mole of alcohol or alkylphenol can be about 1 to about 50, about 10 to about 35, or about 18 to about 27.
- the alkoxylated alcohol or alkoxylated alkylphenol can then be reacted with acrylonitrile to form a nitrile which can then be reduced with a hydrogenation reagent to form a polyetheramine.
- the polyetheramine can be represented by the formula RO(R 1 O) x CH 2 CH 2 CH 2 NH 2 where R represents the hydrocarbon group of the alcohol or alkylphenol, R 1 represents the hydrocarbon group of the alkylene oxide, and x represents the number of moles of alkylene oxide reacted with one mole of alcohol or alkylphenol.
- R represents the hydrocarbon group of the alcohol or alkylphenol
- R 1 represents the hydrocarbon group of the alkylene oxide
- x represents the number of moles of alkylene oxide reacted with one mole of alcohol or alkylphenol.
- the nitrogen-containing detergent of this invention can be (A)(I )(c) an alkoxylated reaction product of the reaction product of a fatty carboxylic acid and naphthenic acid and polyethylenepolyamines.
- the fatty carboxylic acid can be linear, branched, or a mixture thereof.
- the fatty carboxylic acid can be saturated, unsaturated, or a mixture thereof.
- the fatty carboxylic acid can have about 4 to about 22, about 6 to about 22, or about 10 to about 20 carbon atoms.
- the fatty carboxylic acid is oleic acid or stearic acid.
- the naphthenic acid can be derived from petroleum and is a mixture of saturated carboxylic acids of about 180 to about 350 molecular weight that generally contain cyclic groups.
- the polyethylenepolyamines can contain about 3 to about 10, about 3 to about 8, or about 3 to about 6 nitrogen atoms and include for example diethylenetriamine and triethylenetetramine.
- the reaction product of the fatty acid, naphthenic acid and polyethylenepolyamines can be alkoxylated with an alkylene oxide which can have about 2 to about 10, about 2 to about 8, or about 2 to about 6 carbon atoms and includes ethylene oxide, propylene oxide, butylene oxide, and mixtures thereof.
- the mole ratio of the fatty acid to naphthenic acid can be respectively about 0.1 to 1:0.1 to 1.
- the amount of the polyethylenepolyamines used is generally sufficient or in a small excess to react with all the carboxylic groups of the fatty and naphthenic acids.
- naphthenic acid is reacted with oleic acid and triethylenetetramine at about 220 to about 26O 0 C to form an intermediate which is further reacted with ethylene oxide at about 160 to about 18O 0 C where the weight ratio of the reactants is respectively about 1:1.2:0.7:0.2.
- the nitrogen-containing detergent and additive (A) is (A)(l)(a) a Mannich detergent, (A)(l)(b) a polyetheramine, or a mixture thereof.
- the fatty acid derived friction modifier of the invention can be (A)(2)(a) a polyalkoxylated fatty amine.
- Polyalkoxylated fatty amines are available commercially and are generally prepared by reacting a fatty carboxylic acid with ammonia to form an amide which is then reduced to a primary fatty amine with a hydrogenation reagent.
- the hydrocarbon group of the fatty amine can be straight chained, branched chained, or a mixture thereof.
- the hydrocarbon group of the fatty amine can be saturated, unsaturated, or a mixture thereof.
- the hydrocarbon group of the fatty amine can have about 4 to about 22, about 6 to about 22, or about 10 to about 20 carbon atoms.
- the fatty amine is generally further reacted with an alkylene oxide, such as for example a C 2 -C 4 alkylene oxide like ethylene oxide, in a ratio of 2 or more moles of alkylene oxide per mole of fatty amine to form the polyalkoxylated fatty amine.
- the mole ratio of alkylene oxide to fatty amine can be about 2 to 50:1, about 2 to 20:1, about 2 to 10:1; or about 2 to 4:1.
- the polyalkoxylated fatty amine is a diethoxylated tallowamine or a diethoxylated oleylamine.
- the fatty acid derived friction modifier of the invention can be (A)(2)(b) a fatty acid derived oxazoline.
- the oxazoline can be prepared from the reaction of a fatty carboxylic acid and 2-aminoethanol or a derivative thereof having a primary amino group on a carbon beta to a carbon having a hydroxy group such as for example trishydroxymethylaminomethane (THAM).
- THAM trishydroxymethylaminomethane
- the fatty carboxylic acid can be an acid as described above in paragraph [0017] for subcomponent (A)(l)(c).
- the oxazoline is the reaction product of stearic acid and 2-aminoethanol.
- the oxazoline is the reaction product of isostearic acid and THAM.
- the mole ratio of fatty acid to 2-aminoethanol or a derivative thereof is 0.5 to 4:1, 1 to 3:1, 1.4 to 2.6:1, 2:1, or 1:1.
- the oxazoline can be prepared by reacting the fatty acid and the amino ethanol or derivative thereof at elevated temperatures of about 90 to about 200 0 C with the removal of water from the reaction.
- the fatty acid derived friction modifier and additive (A) is (A)(2)(a) a polyalkoxylated fatty amine, (A)(2)(b) a fatty acid derived oxazoline, or (A)(2)(c) a mixture thereof.
- the solid organic matrix material (B) of the invention can be any material which when combined with additive (A) produces or results in an additive composition which is a solid.
- Component (B) can comprise (1) a hydrocarbon; (2) an alcohol; (3) an organic acid, a derivative of an organic acid, or a mixture thereof; (4) an organic compound other than (B)(1)-(B)(3) containing only atoms selected from the group consisting of carbon, hydrogen, oxygen and nitrogen; or (5) a mixture thereof.
- Component (B) can have a melting point of or greater than about 25 0 C, of or greater than about 5O 0 C, of or greater than about 6O 0 C, in the range of about 25 to about 200 0 C, in the range of about 25 to about 100 0 C, in the range of about 50 to about 200 0 C, or in the range of about 50 to about 100 0 C.
- the hydrocarbon (B)(I) can be natural, synthetic, or a mixture thereof.
- Natural hydrocarbons can comprise petroleum waxes including a paraffin or a mixture of paraffins where the paraffin or paraffins have sufficiently high molecular weights of about 254 or higher so that they are a solid such as for example a Ci 8 H 3S or C 36 H 74 or C 24 H 50 paraffin.
- Synthetic hydrocarbons can comprise polyethylenes, hydrocarbons from a Fischer-Tropsch process, or a mixture thereof such as for example a linear low density polyethylene or a Fischer-Tropsch hydrocarbon wax.
- the alcohol (B)(2) can be linear, branched, or a mixture thereof.
- Linear alcohols that are solids generally have a molecular weight of 214 or higher such as for example a Ci 4 H 2 CiOH or C] 6 H 33 OH or Ci 8 H 37 OH alcohol.
- Component (B)(3) can comprise an organic acid, a derivative of an organic acid, or a mixture thereof.
- the organic acid can comprise a linear carboxylic acid, a branched carboxylic acid, an aromatic carboxylic acid, or a mixture thereof.
- Linear carboxylic acids that are solids will generally have about 10 or more carbon atoms such as for example decanoic acid and dodecanoic acid.
- Aromatic acids can include for example benzoic acid and a naphthoic acid.
- Derivatives of organic acids can comprise esters of carboxylic acids which can comprise natural esters, synthetic esters, or a mixture thereof.
- Natural esters can comprise esters from animal sources such as beeswax, esters from vegetable sources such as carnauba wax, or a mixture thereof.
- Synthetic esters can comprise an aromatic carboxylic acid or a fatty carboxylic acid ester of a polyol.
- the fatty acid can be linear, branched, or a mixture thereof.
- the fatty acid can have about 8 to about 22, about 10 to about 22, or about 12 to about 20 carbon atoms.
- the fatty acid can be saturated, unsaturated, or a mixture thereof.
- the polyol can have 2 or more hydroxy groups or can have 3 or more hydroxy groups to include for example glycerol and sorbitol.
- the synthetic ester can include for example sorbitan tristearate, glyceryl tristearate, and glyceryl tribenzoate.
- component (B)(3) can comprise a linear fatty carboxylic acid, an aromatic carboxylic acid, a natural ester, a synthetic ester derived from a polyol and a linear fatty carboxylic acid or an aromatic carboxylic acid, or a mixture thereof.
- the component (B)(4) can comprise an organic compound as described above to include a poly(ethylene glycol), an ethylcellulose, or a mixture thereof.
- the poly(ethylene glycol) can have a number average molecular weight of or greater than about 400, about 600, or about 900.
- the additive composition of this invention can comprise components (A) and (B), as described above, where the additive composition is a solid.
- the additive composition can be a solid that melts at or greater than about 25 0 C, at or greater than about 5O 0 C, at or greater than about 6O 0 C, in the range of about 25 to about 200 0 C, in the range of about 25 to about 100 0 C, in the range of about 50 to about 200 0 C, or in the range of about 50 to about 100 0 C.
- the weight % ratio of component (A) to component (B) in the additive composition can be respectively about 5-95:95-5, about 15-85:85-15, or about 25-75:75-25.
- Components (A) and (B) can each be present in the additive composition on a weight basis at about 5 to about 95%, about 15 to about 85%, or about 25 to about 75%.
- the additive composition comprising the additive (A) and the solid organic matrix material (B) and any other components, can be prepared in any process or procedure that results in a solid additive composition or in a homogeneous solid additive composition.
- the additive composition can generally be prepared by combining the components and mixing the combination at an ambient temperature or at an elevated temperature. The combining of components can be by putting all of them together at the start of the preparation process or by adding one or more components to one or more components simultaneously or sequentially.
- the mixing can be carried out by any mixing means or mixing device comprising a mixer such as for example a stirrer, an agitator or a dispersator; a grinding mill such as for example a ball mill, a rod mill or a tube mill; a sonic device; a blending system employing in-line dynamic (moving) or static (nonmoving) mixing elements to agitate or mix together a stream of components; or a combination thereof, hi one embodiment of the invention where component (B) or any other of the components is a low melting solid generally melting at or below about 100 0 C, the additive composition can be prepared by combining the components, applying sufficient heat to melt the solid components mixing the components mixing means or device such as a mixer, and allowing the mixture to cool to form a solid additive composition, hi another embodiment of the invention where component (B) or any other of the components is a high melting solid generally melting above about 100 0 C, the additive composition can be prepared by combining the components and mixing them with a mixing means or mixing device such as a grinding
- the solid mixture can be further processed by compression into a pellet, tablet or pill shape by using any of the methods for manufacture of pellets from powders known to those skilled in the art. This includes the use of a pressurized die, such as is used for making KBr pellets for recording infrared spectra of solids, or an automated form of this process such as by use of a pelletizing machine, which converts powders to tablets.
- the solid can also be processed into granular form by any of the readily available techniques known to those skilled in the art for granularization,
- the additive (A) of the present invention can be a gel.
- the gel can comprise component (A)(I), component (A)(2) or a mixture thereof dissolved or dispersed in a gel composition.
- the gel composition can comprise one or more additives in the form of an additive gel that slowly releases an additive component or components into a functional fluid such as a lubricant or fuel composition.
- the one or more additives comprising the gel composition can be selected from detergents, dispersants, acids, bases, overbased detergents and combinations thereof, hi one embodiment of the invention the gel composition can further comprise additional fuel or lubricant additives comprising metal-containing detergents such as overbased sulfonates, dispersants such as polyisobutenylsuccinimides, extreme pressure and antiwear agents such as zinc dithiophosphates, antioxidants such as hindered phenols and derivatives thereof, auxiliary friction modifiers such as fatty acid based imidazolines, corrosion and rust inhibitors such as polyisobutenylsuccinic acids, viscosity modifiers such as nitrogen-containing esters of maleic anhydride-styrene copolymers, auxiliary nitrogen-containing detergents such as hydrocarbon- substituted amines derived from polyisobutylene, seal swell agents such as sulfolanes, antifoamants such as silicone oils, metal deactivators such as tolyltriazole
- additive (A) comprising (A)(I), (A)(2), or (A)(3), can be dissolved or dispersed into the gel composition to form a gel before, during or after the preparation of the gel composition.
- the additive composition of the present invention can be prepared or fabricated in a dosage unit for convenient use in a given application such as for example an after-market treatment of a functional fluid to enhance its performance.
- the additive composition can be fabricated as an uncoated dosage unit or as a coated dosage unit.
- the coating can be nontoxic; soluble in a hydrocarbon medium comprising an oil of lubricating viscosity such as a natural and/or synthetic lubricating oil or base stock, or a hydrocarbon fuel such as a gasoline or diesel fuel; and have a melting point of about 5O 0 C or higher, about 6O 0 C or higher, about 65 0 C or higher, or about 75 0 C or higher.
- the coating can comprise one or more of the solid organic matrix materials of component (B) described above in paragraph [0022] or a wrapper such as for example an aluminum foil wrapper.
- the dosage unit can be prepared or fabricated by procedures known in the art such as processing the additive composition in a semi-solid to solid state through for example a pellet mill or an extruder to form the additive composition in a dosage unit or processing the additive composition in a melt or liquid state into a dosage size mold or into a mold from which dosage units can be prepared.
- the additive composition comprising components (A) and (B) is fabricated as a dosage unit in a dosing device.
- the fabrication of the additive composition as a dosage unit in a dosing device can be done by processing the additive composition in a melt or liquid state into a dosage-sized dosing device such as for example a cylindrical container which after further fabrication allows for insertion or injection into a functional fluid.
- the additive composition of this invention optionally can further comprise (C) at least one additional additive.
- the additional additive (C) can comprise one or more of the additional fuel or lubricant additives described in paragraph [0025] which the gel composition can further comprise.
- a method to enhance performance of a functional fluid comprises adding a performance enhancing amount of the solid additive composition, as described throughout this application, to the functional fluid.
- the enhancement in performance comprises maintaining performance of a fluid with for example a keep clean dose or doses, improving performance of a fluid with for example a clean up dose or doses, extending the life of a fluid with for example one or more supplemental doses, restoring performance of a functional fluid with for example one or more fixative doses, or a combination thereof.
- the method of the present invention employing an additive composition in a concentrated solid form to enhance performance of a functional fluid is effective, convenient and safe.
- the solid additive composition fabricated in dosage units that are coated and/or in a dosing device simplifies treating a functional fluid including sealed fluids such as gear oils and transmission fluids, requires no measuring or handling of solvents or diluents, and eliminates or minimizes contact with additives.
- the solid additive composition can be fabricated in dosage units to deliver on a weight basis 1 to 100,000 ppm (parts per million), 1 to 10,000 ppm or 10 to 1,000 ppm actives to a functional fluid, hi an embodiment of the method of the invention the functional fluid is a functional fluid for a vehicle powered by an internal combustion engine to include a spark-ignited or compression-ignited engine, and in other embodiments the functional fluid for the vehicle powered by an internal combustion engine comprising a motor oil, a fuel composition, a power transmission fluid, a gear oil, and a hydraulic fluid.
- the functional fluid is a fuel composition comprising a major amount of a hydrocarbon fuel comprising a gasoline or diesel fuel and a minor amount of the solid additive composition, or the functional fluid is a power transmission fluid comprising a major amount of an oil of lubricating viscosity and a minor amount of the solid additive composition.
- the solid additive composition rapidly dissolves in the functional fluid in or less than about 1 minute to about 1 hour, or gradually dissolves in the functional fluid from greater than about 1 hour to about 1 month.
- a solid additive composition is prepared by combining about 7g of a polyetheramine and about 14g of a linear Ci 6 -C 18 alcohol, melting and mixing this combination, and allowing the melted mixture to solidify in a syringe cylinder modified to have an open end.
- the polyetheramine is prepared by reacting a Ci 3 alcohol with butylene oxide in respectively about a 1 :20 mole ratio and reacting the polyalkoxylated alcohol with acrylonitrile to form a nitrile which is catalytically hydrogenated to form the polyetheramine.
- the fuel additive "stick" is injected from the modified syringe into a partially filled 20-gallon gasoline tank of a vehicle powered by a spark-ignited engine and the tank is filled up.
- the gasoline in the tank is found to contain 1 about 00 ppm by weight of the polyetheramine which has been shown to be an effective level for keeping intake valves clean.
- a solid additive composition is prepared by combining about 2.4g of a diethoxylated tallowamine friction modifier and about 12.6g of an oxazoline friction modifier and about 15g of a paraffin wax, melting and mixing this combination, and allowing the melted mixture to solidify in a syringe modified to have an open end.
- the oxazoline is prepared by reacting isostearic acid with trishydroxymethylaminomethane in respectively about a 2:1 mole ratio with removal of reaction water.
- the lubricant additive "stick" in the modified syringe is divided into about 2.5g pellets. A pellet is inserted into a seal-for-life automatic transmission having a "noise" performance problem.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- Solid Fuels And Fuel-Associated Substances (AREA)
- Lubricants (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Detergent Compositions (AREA)
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2008504228A JP2008534746A (en) | 2005-03-29 | 2006-03-27 | Solid additive composition and method thereof |
CA002603007A CA2603007A1 (en) | 2005-03-29 | 2006-03-27 | Solid additive composition and method thereof |
EP06739737A EP1877527A1 (en) | 2005-03-29 | 2006-03-27 | Solid additive composition and method thereof |
BRPI0607587-8A BRPI0607587A2 (en) | 2005-03-29 | 2006-03-27 | solid additive composition and method for increasing the performance of a functional fluid |
AU2006230103A AU2006230103A1 (en) | 2005-03-29 | 2006-03-27 | Solid additive composition and method thereof |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/092,403 | 2005-03-29 | ||
US11/092,403 US20060229215A1 (en) | 2005-03-29 | 2005-03-29 | Solid additive compostion and method thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2006105025A1 true WO2006105025A1 (en) | 2006-10-05 |
Family
ID=36759040
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2006/011121 WO2006105025A1 (en) | 2005-03-29 | 2006-03-27 | Solid additive composition and method thereof |
Country Status (8)
Country | Link |
---|---|
US (1) | US20060229215A1 (en) |
EP (1) | EP1877527A1 (en) |
JP (1) | JP2008534746A (en) |
CN (1) | CN101184831A (en) |
AU (1) | AU2006230103A1 (en) |
BR (1) | BRPI0607587A2 (en) |
CA (1) | CA2603007A1 (en) |
WO (1) | WO2006105025A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014102150A1 (en) | 2012-12-27 | 2014-07-03 | Shell Internationale Research Maatschappij B.V. | Compositions |
US9315754B2 (en) | 2012-12-27 | 2016-04-19 | Shell Oil Company | Compositions |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8022021B2 (en) * | 2007-02-05 | 2011-09-20 | The Lubrizol Corporation | Low ash controlled release gels |
WO2010039509A2 (en) * | 2008-10-02 | 2010-04-08 | The Lubrizol Corporation | Delivery of substantially insoluble additives to functional fluids |
CN104120000A (en) * | 2009-01-20 | 2014-10-29 | 卢布里佐尔公司 | Hydraulic composition with improved wear properties |
FR2977895B1 (en) * | 2011-07-12 | 2015-04-10 | Total Raffinage Marketing | ADDITIVE COMPOSITIONS ENHANCING STABILITY AND MOTOR PERFORMANCE OF NON-ROAD GASES |
US9506008B2 (en) | 2013-12-23 | 2016-11-29 | Exxonmobil Research And Engineering Company | Method for improving engine fuel efficiency |
CN104099142B (en) * | 2014-07-14 | 2016-08-24 | 周伟明 | A kind of fuel assistants and its production and use |
CN104774658B (en) * | 2015-03-10 | 2017-01-25 | 重庆思派恩环保科技有限公司 | Solid fuel additive |
CN105018193A (en) * | 2015-06-15 | 2015-11-04 | 赵兰 | Train specific mineral hydraulic oil and preparation method therefor |
CA3144386A1 (en) * | 2019-06-24 | 2020-12-30 | The Lubrizol Corporation | Continuous acoustic mixing for performance additives and compositions including the same |
CN110591798A (en) * | 2019-09-25 | 2019-12-20 | 上海德联化工有限公司 | Engine oil with cleaning function for engine and preparation method thereof |
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WO2005003266A1 (en) * | 2003-06-25 | 2005-01-13 | The Lubrizol Corporation | Novel additive composition that reduces soot and/or emissions from engines |
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GB9716283D0 (en) * | 1997-08-01 | 1997-10-08 | Exxon Chemical Patents Inc | Lubricating oil compositions |
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MY126005A (en) * | 2001-03-23 | 2006-09-29 | Filton Ind Sdn Bhd | Diesel fuel filters containing smoke suppressant, and a method of slow releasing said suppressant |
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US6843916B2 (en) * | 2002-07-16 | 2005-01-18 | The Lubrizol Corporation | Slow release lubricant additives gel |
-
2005
- 2005-03-29 US US11/092,403 patent/US20060229215A1/en not_active Abandoned
-
2006
- 2006-03-27 CA CA002603007A patent/CA2603007A1/en not_active Abandoned
- 2006-03-27 WO PCT/US2006/011121 patent/WO2006105025A1/en active Application Filing
- 2006-03-27 JP JP2008504228A patent/JP2008534746A/en not_active Withdrawn
- 2006-03-27 EP EP06739737A patent/EP1877527A1/en not_active Withdrawn
- 2006-03-27 BR BRPI0607587-8A patent/BRPI0607587A2/en not_active IP Right Cessation
- 2006-03-27 AU AU2006230103A patent/AU2006230103A1/en not_active Abandoned
- 2006-03-27 CN CNA2006800185270A patent/CN101184831A/en active Pending
Patent Citations (6)
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GB1455250A (en) * | 1972-12-13 | 1976-11-10 | Century Oils Ltd | Corrosion inhibitng preparations |
US4375418A (en) * | 1981-10-28 | 1983-03-01 | Texaco Inc. | Lubricating oil composition |
US6312480B1 (en) * | 1998-02-06 | 2001-11-06 | Basf Aktiengesellschaft | Solid fuel additive |
US6835218B1 (en) * | 2001-08-24 | 2004-12-28 | Dober Chemical Corp. | Fuel additive compositions |
WO2005003266A1 (en) * | 2003-06-25 | 2005-01-13 | The Lubrizol Corporation | Novel additive composition that reduces soot and/or emissions from engines |
WO2005123238A1 (en) * | 2004-06-11 | 2005-12-29 | Honeywell International, Inc. | Automotive additive composition |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2014102150A1 (en) | 2012-12-27 | 2014-07-03 | Shell Internationale Research Maatschappij B.V. | Compositions |
US9315754B2 (en) | 2012-12-27 | 2016-04-19 | Shell Oil Company | Compositions |
US9382490B2 (en) | 2012-12-27 | 2016-07-05 | Shell Oil Company | Compositions |
Also Published As
Publication number | Publication date |
---|---|
EP1877527A1 (en) | 2008-01-16 |
CA2603007A1 (en) | 2006-10-05 |
BRPI0607587A2 (en) | 2009-09-15 |
AU2006230103A1 (en) | 2006-10-05 |
JP2008534746A (en) | 2008-08-28 |
CN101184831A (en) | 2008-05-21 |
US20060229215A1 (en) | 2006-10-12 |
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