US20080086934A1 - Protecting fuel delivery systems in engines combusting ethanol-containing fuels - Google Patents

Protecting fuel delivery systems in engines combusting ethanol-containing fuels Download PDF

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Publication number
US20080086934A1
US20080086934A1 US11/549,860 US54986006A US2008086934A1 US 20080086934 A1 US20080086934 A1 US 20080086934A1 US 54986006 A US54986006 A US 54986006A US 2008086934 A1 US2008086934 A1 US 2008086934A1
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United States
Prior art keywords
fuel
ethanol
additive
gasoline
dispersants
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Abandoned
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US11/549,860
Inventor
Lawrence J. Cunningham
Richard J. DuMont
William J. Colucci
Alexander M. Kulinowski
Joseph W. Roos
Ronald K. Fricke
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Afton Chemical Corp
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Afton Chemical Corp
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Priority to US11/549,860 priority Critical patent/US20080086934A1/en
Assigned to AFTON CHEMICAL CORPORATION reassignment AFTON CHEMICAL CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: COLUCCI, WILLIAM J., DUMONT, RICHARD J., FRICKE, RONALD K., CUNNINGHAM, LAWRENCE J., KULINOWSKI, ALEXANDER M., ROOS, JOSEPH W.
Assigned to SUNTRUST BANK reassignment SUNTRUST BANK SECURITY AGREEMENT Assignors: AFTON CHEMICAL CORPORATION
Priority to EP07253982A priority patent/EP1914290A1/en
Priority to BRPI0704159-4A priority patent/BRPI0704159A/en
Publication of US20080086934A1 publication Critical patent/US20080086934A1/en
Assigned to AFTON CHEMICAL CORPORATION reassignment AFTON CHEMICAL CORPORATION RELEASE BY SECURED PARTY (SEE DOCUMENT FOR DETAILS). Assignors: SUNTRUST BANK
Abandoned legal-status Critical Current

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    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
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    • C10L1/14Organic compounds
    • C10L1/22Organic compounds containing nitrogen
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    • C10L1/224Amides; Imides carboxylic acid amides, imides
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    • C10L10/04Use of additives to fuels or fires for particular purposes for minimising corrosion or incrustation
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    • C10L10/00Use of additives to fuels or fires for particular purposes
    • C10L10/10Use of additives to fuels or fires for particular purposes for improving the octane number
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F02COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
    • F02BINTERNAL-COMBUSTION PISTON ENGINES; COMBUSTION ENGINES IN GENERAL
    • F02B47/00Methods of operating engines involving adding non-fuel substances or anti-knock agents to combustion air, fuel, or fuel-air mixtures of engines
    • F02B47/04Methods of operating engines involving adding non-fuel substances or anti-knock agents to combustion air, fuel, or fuel-air mixtures of engines the substances being other than water or steam only
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    • C10L1/182Organic compounds containing oxygen containing hydroxy groups; Salts thereof
    • C10L1/1822Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms
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    • C10L1/182Organic compounds containing oxygen containing hydroxy groups; Salts thereof
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    • C10L1/1985Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds homo- or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon to carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid polyethers, e.g. di- polygylcols and derivatives; ethers - esters
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    • Y02T10/10Internal combustion engine [ICE] based vehicles
    • Y02T10/12Improving ICE efficiencies

Definitions

  • the present disclosure relates to the use of fuel additives in duel delivery systems contacting or combusting fuels containing ethanol.
  • the additives improve the properties of the resulting fuel, minimize the impact of the fuel on the components of the fuel delivery system and also enhance the benefits to the consumer and to the environment of utilizing varying amounts of ethanol as a fuel in combustion engines.
  • E85 fuel A common blend of gasoline and ethanol being discussed is 15% gasoline and 85% ethanol, often commonly referred to as “E85” fuel (hereinafter “E85”).
  • Other ethanol fuels can comprise, for example 10% ethanol (E10) and 100% ethanol (E100).
  • ethanol alone or in gasoline blends can create new problems for fuel equipment designed to handle the more non-polar hydrocarbonaceous petroleum fractions commonly known as gasolines.
  • the polarity, corrosivity, adhesiveness, friction properties, and perhaps conductivity of ethanol or ethanol-containing fuel can create new problems and new needs in the fuel industry.
  • E85, gasoline, and diesel are seasonally adjusted to ensure proper starting and performance in different geographic locations.
  • E85 sold during colder months often contain only 70% ethanol and then 30% petroleum additives to produce the necessary vapor pressure for starting in cold temperatures.
  • the petroleum additive content for E85 can often be, for example, 17% to about 20%.
  • the need for better cold start performance and reliability will increase.
  • ethanol is widely treated with additives designed to prevent human consumption.
  • Such treated ethanol is called denatured alcohol, or denatured ethanol and common denaturants include gasoline, gasoline components, and kerosene.
  • Other denaturants for rendering fuel alcohol unfit for beverage use are defined in 27 CFR 21.24.
  • Fuel delivery systems in vehicles combusting gasoline fuels have increasingly complicated componentry, some of which is, can be or will be highly sensitive to variations in certain fuel parameters. Physical and chemical properties of the fuel can negatively impact the performance or life of these fuel delivery systems. Thus, certain components designed for use in traditional gasolines might be susceptible to fatigue, reduce performance or complete failure upon prolonged exposure to fuels containing ethanol, particularly fuels containing high percentages of ethanol, like E85 and E100. Therefore, a need exists to protect such older engines and well as improve the reliability of newer engines when all are exposed to prolonged combustion of ethanol-containing fuels.
  • FFVs flexible fuel vehicles
  • E85 ethanol concentrations of up to 85% by volume
  • Pure ethanol has broader flammability limits than gasoline and burns with lower flame luminosity.
  • the vapor space flammability limits of ethanol approach those of gasoline and luminosity is increased.
  • OGA-480 a polyetheramine available from Chevron Oronite, has been used in E100 fuel but has not been used in E85, nor have other amines been used in ethanol/gasoline blends, to the knowledge of the present inventors.
  • An embodiment presented herein provides fuel additive agents for use in improving the protection of fuel delivery systems of engines combusting ethanol-containing fuels, including but not limited to E100, E85, E50, and the like down to E10 and trace blends of ethanol in gasoline.
  • Another embodiment provides a method to improve protection of a fuel delivery system in an internal combustion engine, said method comprising delivering to and/or combusting in said engine a fuel composition comprising gasoline, ethanol and at least one fuel additive.
  • ethanol herein is meant ethyl alcohol, the chemical compound C 2 H 5 OH. This can arise in or be provided in many qualities or grades, such as a commercial blend or fuel grade, as well as pure or reagent grade ethanol, and can be derived from any source such as but not limited to petroleum refinery streams, distillation cuts, and bio-derived (e.g. bioethanol from corn).
  • a method for improving the protection of internal combustion engines and the fuel delivery system used to convey and deliver the fuel to the combustion engine is provided.
  • the problems that can arise in the delivery and combustion of fuels containing ethanol, and especially high levels of ethanol are addressed by the embodiments within the present claims.
  • the more polar nature of the ethanol as compared to the less polar hydrocarbonaceous gasoline can have a negative impact on, for example, the parts of the engine's combustion surfaces, fuel tank, valves, seals, gaskets, injectors, liners, pumps, hoses, liners, filters, and other components.
  • the ethanol used in the ethanol-gasoline blends of the present disclosure is not necessarily or always pure ethyl alcohol but can and will often contain certain varying amounts of sulfur and sulfur-containing chemicals, acidic or basic components or contaminants, water, possibly ethylene glycol, other alcohols, and petrochemical fractions boiling near ethanol.
  • the bio-source can contribute other natural products and bio-derivatives which can accumulate in or on vulnerable engine and fuel delivery parts.
  • the present disclosure provides fuel compositions and methods for reducing or eliminating the negative impact on the engine or its delivery system from these natural products and bio-derivatives.
  • the present disclosure also provides improved protection of the fuel delivery system by the incorporation of certain fuel additives in the gasoline-ethanol fuel composition.
  • a method to improve protection of a fuel delivery system in an internal combustion engine comprising delivering to or combusting in said engine a fuel composition comprising gasoline, ethanol and at least one fuel additive, said additive being selected from the group consisting of succinimide dispersants, succinamide dispersants, amides, Mannich base dispersants, and polyetheramine dispersants.
  • a fuel composition comprising gasoline, ethanol and at least one fuel additive, said additive being selected from the group consisting of succinimide dispersants, succinamide dispersants, amides, Mannich base dispersants, and polyetheramine dispersants.
  • Polyetheramines are particularly effective in the compositions and methods of the present disclosure.
  • the fuel additive is further selected from the group consisting of phenolics, hindered phenolics, aryl amines, and diphenyl amines.
  • the fuel additive is further selected from the group consisting of monocarboxylic acids, dicarboxylic acids, polycarboxylic acids, p-phenylenediamine and dicyclohexylamine.
  • acid fuel additives are tall oil fatty acids and/or the diacid dodecenyl succinic acid.
  • the fuel additive can be further selected from the group consisting of oxylated alkylphenolic resins, and formaldehyde polymer with 4-(1,1-dimethylethyl)phenol, methyloxirane and oxirane.
  • the fuel additive can be further selected from the group consisting of methyl cyclopentadienyl manganese tricarbonyl (“MMT”), cyclopentadienyl manganese tricarbonyl, azides, tetraethyl lead, peroxides and alkyl nitrates.
  • MMT methyl cyclopentadienyl manganese tricarbonyl
  • azides tetraethyl lead
  • peroxides and alkyl nitrates alkyl nitrates.
  • the fuel additive can further be selected from ethylene oxide, propylene oxide, butylene oxide, epoxides, C1-C8 aliphatic hydrocarbons, nitrous oxide, nitromethane and xylene.
  • the fuel additive is also further selected from the group consisting of monoesters, diesters, ethers, diethyl ether, ketones, diethers, polyethers, glymes and glycols.
  • the fuel additive is selected from the group consisting of monocarboxylic acids, dicarboxylic acids, and polycarboxylic acids.
  • Also provided herein is a method of improving the protection of an engine combusting a fuel composition containing gasoline and ethanol, said method consisting essentially of combining the fuel and an additive selected from the group consisting of driveability enhancing materials that include monoesters, diesters, ethers, ketones, diethers, polyethers, glymes and glycols, wherein the driveability of said engine is improved relative to the driveability of the engine combusting a gasoline fuel without ethanol.
  • the fuel additive is selected from the group consisting of phenates, salicylates, sulfonates, nonylphenol ethoxylates, fuel-soluble alkali detergents and alkaline earth metal-containing detergents.
  • Particularly effective detergents herein include phenates, salicylates, sulfonates, and nonylphenol ethoxylates.
  • a fuel composition comprising, or in another embodiment consisting essentially of, gasoline, ethanol and at least one fuel delivery system protecting agent, said agent being selected from the group consisting of succinimide dispersants, succinamide dispersants, amides, Mannich base dispersants, polyetheramine dispersants, phenolics, hindered phenolics, aryl amines, diphenyl amines, monocarboxylic acids, dicarboxylic acids, polycarboxylic acids, p-phenylenediamine and dicyclohexylarnine, oxylated alkylphenolic resins, formaldehyde polymer with 4-(1,1-dimethylethyl)phenol, methyloxirane and oxirane, methyl cyclopentadienyl manganese tricarbonyl, cyclopentadienyl manganese tricarbonyl, azides, tetraethy
  • a fuel delivery system protecting agent concentrate for gasoline engines combusting an ethanol-containing fuel, said concentrate comprising one or more fuel delivery system protecting agents and a diluent selected from the group consisting of an oil, a fuel, gasoline, ethanol, solvent, carrier fluid, and other liquid materials combustible in a gasoline engine.
  • the ethanol content of the fuel composition is from about 74% to about 85%. In another embodiment of the disclosure herein the ethanol content of the fuel composition is from about 50% to about 74%.
  • New Energy Ethanol 1.6 ADM Ethanol 10.8 New Energy Ethanol is a commercial ethanol with a denaturant ADM Ethanol is ethanol with a corrosion inhibitor (DCI-11, from Innospec) and a denaturant
  • Table 1 shows the intake valve deposits generated on an Intake Valve Deposit simulator rig test using E85 fuels containing the ethanols indicated.
  • the fuel blend is sprayed onto a hot surface and the resulting residue weighed.
  • the base gasoline was Citgo RUL and without any additives the Intake Valve Deposit rating for the base gasoline in the rig test was 12.4 mg.
  • the two different ethanol sources (New Energy and ADM) yielded significant differences, indicating a need for additives and a problem of non-uniformity across ethanol suppliers. While both ethanol products contain a denaturant, the ADM Ethanol is further believed to have 32 PTB of a corrosion inhibitor known commercially as DCI-11 from Innospec.
  • the dosage reported is the treat rate of the additive in the gasoline-ethanol fuel blend.
  • the deposits varied.
  • this table used the ethanol contributing the lowest deposit level (New Energy Ethanol), so other ethanol sources, such as ADM Ethanol, will clearly have significantly more need for detergents, dispersants and other fuel additives, and
  • the deposits shown in Table 2 will include about 1.6 mg of deposits from the New Energy Ethanol in the E85 fuel.
  • additives that generated deposits of about 2.7 mg or less, the total effective deposit not coming from the ethanol is essentially zero, that is, the present disclosure shows in at least these embodiments virtually complete prevention of deposits and the resulting wear on the engine.
  • additives include 2,6-di t-butyl phenol antioxidant, methylcyclopentadienyl manganese tricarbonyl combustion improver and octane enhancer, oleic acid plus N,N dimethylcyclohexylamine, dodecenyl succinic acid, polyisobutylene amine dispersant, 1,2 propane diamine salicylaldehyde metal deactivator, cresol Mannich dispersant, diethanol amide of isostearic acid friction modifier, and 2-ethyl hexyl nitrate combustion improver.
  • the alkyl nitrate, 2-ethyl hexyl nitrate was particularly effective in reducing deposits and hence improving the protection of a fuel delivery system in the
  • a method of improving protection of a fuel delivery system in an internal combustion engine combusting an ethanol-gasoline blend comprising combining the blend with at least one additive selected from the group consisting of 2,6-di t-butyl phenol antioxidant, methylcyclopentadienyl manganese tricarbonyl combustion improver and octane enhancer, oleic acid plus N,N dimethylcyclohexylamine, dodecenyl succinic acid, polyisobutylene amine dispersant, 1,2 propane diamine salicylaldehyde metal deactivator, cresol Mannich base dispersant, diethanol amide of isostearic acid friction modifier, and 2-ethyl hexyl nitrate combustion improver, whereby the deposits formed in said engine are less than the deposits formed in the engine when combusting the blend without the at least one additive.
  • at least one additive selected from the group consisting of 2,6-di t-butyl phenol antioxidant,
  • a Keep Clean Test was performed by driving a Chevrolet Impala for 5,000 miles using fuel containing gasoline without ethanol, and fuel containing E85 blend.
  • the Intake Valve Deposits (IVD) and the Combustion Chamber Deposits (CCD) were then measured and are reported in Table 3.
  • the ethanol used in the E85 blend was ADM Ethanol except for Test No 6 where New Energy Ethanol was used.
  • the use of the dispersant reduced the IVD deposits from 429 mg to 5 mg.
  • the E85 fuel blend of Test No. 3 at a 5 PTB treat rate of the Mannich dispersant in the finished fuel had a IVD deposit of 191 mg but when the dispersant was lacking from the E85 blend (Test No. 5), the IVD deposit went up to 227, due in part to the contribution from the ethanol. Comparing Test No. 3 and Test No. 4 also shows that reducing the ethanol content in the fuel blend from 84% to 74% reduced the deposits from 299 mg to 265 mg. This further illustrates that gasoline ethanol blends will need better dispersancy and detergency. Test No.
  • Test No. 7 shows the result from a higher treat rate (500 PTB) of a polyetheramine dispersant and the result when combusting the E85 fuel was an remarkably low 4 mg of deposit, at least a major portion of which can be attributed to the ethanol by comparing to Test No. 6.
  • the present disclosure provides a method to improve protection of a fuel delivery system in an engine combusting an ethanol-containing fuel by adding to the fuel a polyetheramine dispersant or a Mannich dispersant. It is therefore expected that the combination thereof will have similar or even enhanced and synergistic results.
  • the reduction of deposit formation is directly related to increased longevity of the useful life of engine combustion surfaces, injectors, valves, gaskets, liners, seals, hoses, pumps, filters, and other fuel delivery system parts.
  • a fuel composition is prepared by combining gasoline (15% by volume) and ethanol (85% by volume) and a Mannich base fuel additive (HiTEC® 6560 available from Afton Chemical Corporation, and having a PIB group with a MW of 950, and a cresol group reacted with dibutylamine).
  • the fuel additive is present in the fuel composition at 200 ppm.
  • the composition is fed to and combusted in a direct injection gasoline engine.
  • the resulting fuel will demonstrate improved protection provided in the combustion engine and fuel delivery system compared to the protection resulting before and after combustion of a fuel composition not containing ethanol, as well as compared to the combustion of a fuel composition containing ethanol and gasoline but no Mannich base fuel additive.
  • a fuel composition is prepared by combining gasoline (15% by volume) and ethanol (85% by volume) and an alkylated succinimide dispersant (HiTEC® 4249 available from Afton Chemical Corporation, and having a PIB group with a MW of 950, and a maleic anhydride reacted with tetraethylene pentamine).
  • the dispersant is present in the fuel composition at 100 ppm.
  • the composition is fed to and combusted in a spark ignited internal combustion engine.
  • the resulting fuel demonstrates improved protection in an internal combustion engine and its delivery system compared to the combustion of a fuel composition not containing ethanol, as well as compared to the combustion of a fuel composition containing ethanol and gasoline but no alkylated succinimide dispersant.
  • a fuel composition is prepared by combining gasoline (15% by volume) and ethanol (85% by volume) and a phenolic driveability agent (HiTEC® 4733 available from Afton Chemical Corporation and containing 2,4 di-t-butyl phenol).
  • the antioxidant is present in the fuel composition at 100 ppm.
  • the composition is fed to and combusted in a gasoline engine.
  • the resulting fuel improves protection in an internal combustion engine and its fuel delivery system compared to the combustion of a fuel composition not containing ethanol, as well as compared to the delivery and combustion of a fuel composition containing ethanol and gasoline but no phenolic antioxidant.
  • a fuel composition is prepared by combining gasoline (15% by volume) and ethanol (85% by volume) and a demulsifier agent (Baker Petrolite's Tolad 9372).
  • the demulsifier agent is present in the fuel composition at 30 ppm.
  • the composition is fed to and combusted in an internal combustion gasoline spark ignited engine.
  • the resulting fuel improves the protection in an internal combustion engine and its fuel delivery system compared to the combustion and delivery of a fuel composition not containing ethanol, as well as compared to the combustion and delivery of a fuel composition containing ethanol and gasoline but no demulsifier.
  • a fuel composition is prepared by combining gasoline (15% by volume) and ethanol (85% by volume) and a dehazer agent (2-ethyl hexanol available from BASF).
  • the dehazer agent is present in the fuel composition at 5 weight percent.
  • the composition is fed to and combusted in an internal combustion gasoline spark ignited engine.
  • the resulting fuel improves protection in an internal combustion engine and its delivery system compared to the combustion and delivery of a fuel composition not containing ethanol, as well as compared to the combustion and delivery of a fuel composition containing ethanol and gasoline but no dehazer.
  • a fuel composition is prepared by combining gasoline (15% by volume) and ethanol (85% by volume) and a MMT octane improver (HiTEC® 3000 available from Afton Chemical Corporation).
  • the octane improver is present in the fuel composition at 300 ppm.
  • the composition is fed to and combusted in an internal combustion engine.
  • the resulting fuel improves protection in an internal combustion engine and its delivery system compared to the combustion and delivery of a fuel composition not containing ethanol, as well as compared to the combustion and delivery of a fuel composition containing ethanol and gasoline but no MMT.
  • a fuel composition is prepared by combining gasoline (15% by volume) and ethanol (85% by volume) and a volatility improving agent (2-ethyl hexyl nitrate, HiTEC® 4103 available from Afton Chemical Corporation.
  • the volatility improving agent is present in the fuel composition at 8 weight percent.
  • the composition is fed to and combusted in a gasoline engine.
  • the resulting fuel improves protection in an internal combustion engine and its delivery system compared to the combustion and delivery of a fuel composition not containing ethanol, as well as compared to the delivery and combustion of a fuel composition containing ethanol and gasoline but no volatility improving agent.
  • a fuel composition is prepared by combining gasoline (15% by volume) and ethanol (85% by volume) and a detergent agent (HiTEC® 611 available from Afton Chemical Corporation, and having an overbased calcium sulfonate).
  • the detergent agent is present in the fuel composition at 2.5 weight percent.
  • the composition is fed to and combusted in an internal combustion engine.
  • the resulting fuel improves protection in an internal combustion engine and its delivery system compared to the delivery and combustion of a fuel composition not containing ethanol, as well as compared to the delivery and combustion of a fuel composition containing ethanol and gasoline but no detergent agent.
  • each numerical parameter should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques. Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the disclosure are approximations, the numerical values set forth in the specific examples are reported as precisely as possible. Any numerical value, however, inherently contains certain errors necessarily resulting from the standard deviation found in their respective testing measurements. It is intended that the specification and examples be considered as exemplary only, with a true scope and spirit of the disclosure being indicated by the following claims.

Abstract

The present disclosure relates to the use of fuel additives in duel delivery systems contacting or combusting fuels containing ethanol, such as E85. The additives improve the properties of the resulting fuel, minimize the impact of the fuel on the components of the fuel delivery system, improve the protection of the engine and the fuel delivery system, and also enhance the benefits to the consumer and to the environment of utilizing varying amounts of ethanol as a fuel in combustion engines.

Description

    FIELD
  • The present disclosure relates to the use of fuel additives in duel delivery systems contacting or combusting fuels containing ethanol. The additives improve the properties of the resulting fuel, minimize the impact of the fuel on the components of the fuel delivery system and also enhance the benefits to the consumer and to the environment of utilizing varying amounts of ethanol as a fuel in combustion engines.
  • BACKGROUND
  • Much has been said about the use of ethanol as a fuel by itself, and also as a blend component for use with gasoline, and even with diesel fuels. Ethanol can be produced from crops and thus provides a viable renewable fuel source.
  • A common blend of gasoline and ethanol being discussed is 15% gasoline and 85% ethanol, often commonly referred to as “E85” fuel (hereinafter “E85”). Other ethanol fuels can comprise, for example 10% ethanol (E10) and 100% ethanol (E100).
  • The use of ethanol alone or in gasoline blends can create new problems for fuel equipment designed to handle the more non-polar hydrocarbonaceous petroleum fractions commonly known as gasolines. The polarity, corrosivity, adhesiveness, friction properties, and perhaps conductivity of ethanol or ethanol-containing fuel can create new problems and new needs in the fuel industry.
  • E85, gasoline, and diesel are seasonally adjusted to ensure proper starting and performance in different geographic locations. For example, E85 sold during colder months often contain only 70% ethanol and then 30% petroleum additives to produce the necessary vapor pressure for starting in cold temperatures. During warmer months the petroleum additive content for E85 can often be, for example, 17% to about 20%. However, as the interest increases to other fuel blends and to possibly wider use of E100, the need for better cold start performance and reliability will increase.
  • Commercial ethanol is widely treated with additives designed to prevent human consumption. Such treated ethanol is called denatured alcohol, or denatured ethanol and common denaturants include gasoline, gasoline components, and kerosene. Other denaturants for rendering fuel alcohol unfit for beverage use are defined in 27 CFR 21.24.
  • Fuel delivery systems in vehicles combusting gasoline fuels have increasingly complicated componentry, some of which is, can be or will be highly sensitive to variations in certain fuel parameters. Physical and chemical properties of the fuel can negatively impact the performance or life of these fuel delivery systems. Thus, certain components designed for use in traditional gasolines might be susceptible to fatigue, reduce performance or complete failure upon prolonged exposure to fuels containing ethanol, particularly fuels containing high percentages of ethanol, like E85 and E100. Therefore, a need exists to protect such older engines and well as improve the reliability of newer engines when all are exposed to prolonged combustion of ethanol-containing fuels.
  • As currently offered to consumers by several automakers, flexible fuel vehicles (FFVs) are designed to operate on any mixture of gasoline and ethanol—with ethanol concentrations of up to 85% by volume (E85). There is one major difference between an FFV and a conventional gasoline-fueled vehicle—the FFV detects the ethanol/gasoline ratio and makes appropriate adjustments to the engine's ignition timing and air/fuel mixture ratios to account for the ethanol and optimize performance and maintain emissions control. The vehicle must be equipped with an air/fuel ratio map capable of handling the adjustments necessary for optimized performance on both gasoline and E85. Components of the fuel delivery systems on FFVs are also modified and upgraded to be resistant to the corrosive effects of alcohol in the fuel.
  • Much like gasoline, the volatility of E85 must be adjusted seasonally and by geographic region to assure adequate cold start and drive away performance. This is done by increasing the amount of gasoline (typically from 15% to 30% by volume) in blends sold during colder months.
  • Pure ethanol has broader flammability limits than gasoline and burns with lower flame luminosity. When blended with hydrocarbon fuels, the vapor space flammability limits of ethanol approach those of gasoline and luminosity is increased.
  • OGA-480, a polyetheramine available from Chevron Oronite, has been used in E100 fuel but has not been used in E85, nor have other amines been used in ethanol/gasoline blends, to the knowledge of the present inventors.
  • SUMMARY OF THE EMBODIMENTS
  • An embodiment presented herein provides fuel additive agents for use in improving the protection of fuel delivery systems of engines combusting ethanol-containing fuels, including but not limited to E100, E85, E50, and the like down to E10 and trace blends of ethanol in gasoline.
  • Another embodiment provides a method to improve protection of a fuel delivery system in an internal combustion engine, said method comprising delivering to and/or combusting in said engine a fuel composition comprising gasoline, ethanol and at least one fuel additive.
  • It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory only and are intended to provide further explanation of the present disclosure, as claimed.
  • DETAILED DESCRIPTION OF EMBODIMENTS
  • By “ethanol” herein is meant ethyl alcohol, the chemical compound C2H5OH. This can arise in or be provided in many qualities or grades, such as a commercial blend or fuel grade, as well as pure or reagent grade ethanol, and can be derived from any source such as but not limited to petroleum refinery streams, distillation cuts, and bio-derived (e.g. bioethanol from corn).
  • By the present disclosure herein is provided a method for improving the protection of internal combustion engines and the fuel delivery system used to convey and deliver the fuel to the combustion engine. In particular, the problems that can arise in the delivery and combustion of fuels containing ethanol, and especially high levels of ethanol are addressed by the embodiments within the present claims. The more polar nature of the ethanol as compared to the less polar hydrocarbonaceous gasoline can have a negative impact on, for example, the parts of the engine's combustion surfaces, fuel tank, valves, seals, gaskets, injectors, liners, pumps, hoses, liners, filters, and other components. In addition, the ethanol used in the ethanol-gasoline blends of the present disclosure is not necessarily or always pure ethyl alcohol but can and will often contain certain varying amounts of sulfur and sulfur-containing chemicals, acidic or basic components or contaminants, water, possibly ethylene glycol, other alcohols, and petrochemical fractions boiling near ethanol. In addition, when the ethanol is bio-derived, the bio-source can contribute other natural products and bio-derivatives which can accumulate in or on vulnerable engine and fuel delivery parts. The present disclosure provides fuel compositions and methods for reducing or eliminating the negative impact on the engine or its delivery system from these natural products and bio-derivatives. The present disclosure also provides improved protection of the fuel delivery system by the incorporation of certain fuel additives in the gasoline-ethanol fuel composition.
  • In one embodiment is provided a method to improve protection of a fuel delivery system in an internal combustion engine, said method comprising delivering to or combusting in said engine a fuel composition comprising gasoline, ethanol and at least one fuel additive, said additive being selected from the group consisting of succinimide dispersants, succinamide dispersants, amides, Mannich base dispersants, and polyetheramine dispersants. Polyetheramines are particularly effective in the compositions and methods of the present disclosure.
  • In another example the fuel additive is further selected from the group consisting of phenolics, hindered phenolics, aryl amines, and diphenyl amines.
  • In yet another aspect herein, the fuel additive is further selected from the group consisting of monocarboxylic acids, dicarboxylic acids, polycarboxylic acids, p-phenylenediamine and dicyclohexylamine. Particularly useful herein as the acid fuel additives are tall oil fatty acids and/or the diacid dodecenyl succinic acid.
  • In yet another embodiment the fuel additive can be further selected from the group consisting of oxylated alkylphenolic resins, and formaldehyde polymer with 4-(1,1-dimethylethyl)phenol, methyloxirane and oxirane.
  • The fuel additive can be further selected from the group consisting of methyl cyclopentadienyl manganese tricarbonyl (“MMT”), cyclopentadienyl manganese tricarbonyl, azides, tetraethyl lead, peroxides and alkyl nitrates.
  • The fuel additive can further be selected from ethylene oxide, propylene oxide, butylene oxide, epoxides, C1-C8 aliphatic hydrocarbons, nitrous oxide, nitromethane and xylene.
  • The fuel additive is also further selected from the group consisting of monoesters, diesters, ethers, diethyl ether, ketones, diethers, polyethers, glymes and glycols.
  • In still another aspect the fuel additive is selected from the group consisting of monocarboxylic acids, dicarboxylic acids, and polycarboxylic acids.
  • Also provided herein is a method of improving the protection of an engine combusting a fuel composition containing gasoline and ethanol, said method consisting essentially of combining the fuel and an additive selected from the group consisting of driveability enhancing materials that include monoesters, diesters, ethers, ketones, diethers, polyethers, glymes and glycols, wherein the driveability of said engine is improved relative to the driveability of the engine combusting a gasoline fuel without ethanol.
  • In another embodiment the fuel additive is selected from the group consisting of phenates, salicylates, sulfonates, nonylphenol ethoxylates, fuel-soluble alkali detergents and alkaline earth metal-containing detergents. Particularly effective detergents herein include phenates, salicylates, sulfonates, and nonylphenol ethoxylates.
  • Thus the present disclosure can be practiced by producing, conveying, or combusting a fuel composition comprising, or in another embodiment consisting essentially of, gasoline, ethanol and at least one fuel delivery system protecting agent, said agent being selected from the group consisting of succinimide dispersants, succinamide dispersants, amides, Mannich base dispersants, polyetheramine dispersants, phenolics, hindered phenolics, aryl amines, diphenyl amines, monocarboxylic acids, dicarboxylic acids, polycarboxylic acids, p-phenylenediamine and dicyclohexylarnine, oxylated alkylphenolic resins, formaldehyde polymer with 4-(1,1-dimethylethyl)phenol, methyloxirane and oxirane, methyl cyclopentadienyl manganese tricarbonyl, cyclopentadienyl manganese tricarbonyl, azides, tetraethyl lead, peroxides, alkyl nitrates, monoesters, diesters, ethers, diethers, diethyl ether, ketones, polyethers, glycols, glymes, oxiranes, C1-C8 aliphatic hydrocarbons, butylene oxide, propylene oxide, ethylene oxide, epoxides, butane, pentane, xylene, nitrous oxide, nitromethane, phenates, salicylates, sulfonates, nonylphenol ethoxylates, and fuel-soluble alkali detergents and an alkaline earth metal-containing detergents.
  • Also provided herein is a fuel delivery system protecting agent concentrate for gasoline engines combusting an ethanol-containing fuel, said concentrate comprising one or more fuel delivery system protecting agents and a diluent selected from the group consisting of an oil, a fuel, gasoline, ethanol, solvent, carrier fluid, and other liquid materials combustible in a gasoline engine.
  • In one embodiment, the ethanol content of the fuel composition is from about 74% to about 85%. In another embodiment of the disclosure herein the ethanol content of the fuel composition is from about 50% to about 74%.
  • EXAMPLES
  • TABLE 1
    IVD Rig Test Deposits From E85 Fuels
    Ethanol Source Deposit, mg.
    New Energy Ethanol 1.6
    ADM Ethanol 10.8
    New Energy Ethanol is a commercial ethanol with a denaturant
    ADM Ethanol is ethanol with a corrosion inhibitor (DCI-11, from Innospec) and a denaturant
  • Table 1 shows the intake valve deposits generated on an Intake Valve Deposit simulator rig test using E85 fuels containing the ethanols indicated. In this rig test, the fuel blend is sprayed onto a hot surface and the resulting residue weighed. The base gasoline was Citgo RUL and without any additives the Intake Valve Deposit rating for the base gasoline in the rig test was 12.4 mg. As can be seen, the two different ethanol sources (New Energy and ADM) yielded significant differences, indicating a need for additives and a problem of non-uniformity across ethanol suppliers. While both ethanol products contain a denaturant, the ADM Ethanol is further believed to have 32 PTB of a corrosion inhibitor known commercially as DCI-11 from Innospec. As can be seen by comparing the rig test deposits from these two ethanols when used in E85 gasoline-ethanol fuel blend, the ADM Ethanol generated a 10-fold increase in deposits relative to the deposits from the New Energy Ethanol. Such an E85 fuel will therefore need more detergents, dispersants and other additives than E85 fuels utilizing other ethanol sources to prolong the useful life of the engine and fuel delivery system.
  • TABLE 2
    IVD Rig Test Deposits on E85 Fuel Containing Additives
    Dosage,
    Additive in ptb Deposit, mg
    H-4733 10 1.4
    H-3000 25 0.9
    H-4142 50 1.0
    H-4848A 50 12.7
    H-4247 38 15.6
    DDSA 50% 25 0.5
    H-6560 100 4.0
    AP-5000 100 2.1
    H-4705 20 1.5
    GAR515A01 100 2.7
    H-6457 50 2.7
    H-4858 50 18.9
    H-6400 100 6.6
    H-4103 5000 ppmv 0.4
    H-4733 is 2,6-di t-butyl phenol antioxidant
    H-3000 is methylcyclopentadienyl manganese tricarbonyl
    H-4142 is oleic acid plus N,N dimethylcyclohexylamine
    H-4848A is diethanol amide, demulsifier, aromatic solvent
    H-4247 is succinimide dispersant and aromatic solvent
    DDSA 50% is dodecenyl succinic acid in A150 solvent
    H-6560 is Mannich base dispersant from dibutyl amine
    AP-5000 is BASF polyisobutylene amine dispersant
    H-4705 is 1,2 propane diamine salicylaldehyde metal deactivator
    GAR515A01 is a cresol Mannich dispersant from dibutyl amine; and polyol
    H-6457 is diethanol amide of isostearic acid friction modifier
    H-4858 is ethylene glycol ester-based lubricity additive
    H-6400 is polyetheramine and DDS corrosion inhibitor, Tolad demulsifier, Aromatic solvent
    H-4103 is 2-ethyl hexyl nitrate combustion improver
    Ptb is pounds per thousand barrels

    Table 1 shows the intake valve deposits generated on the Intake Valve Deposit simulator rig test using E85 fuels containing the New Energy Ethanol. The dosage reported is the treat rate of the additive in the gasoline-ethanol fuel blend. As can be seen by comparing the rig test deposits from these additives when used in the E85 gasoline-ethanol fuel blend, the deposits varied. However, it must be noted that (a) this table used the ethanol contributing the lowest deposit level (New Energy Ethanol), so other ethanol sources, such as ADM Ethanol, will clearly have significantly more need for detergents, dispersants and other fuel additives, and (b) the deposits shown in Table 2 will include about 1.6 mg of deposits from the New Energy Ethanol in the E85 fuel. Thus, for at least those additives that generated deposits of about 2.7 mg or less, the total effective deposit not coming from the ethanol is essentially zero, that is, the present disclosure shows in at least these embodiments virtually complete prevention of deposits and the resulting wear on the engine. These additives include 2,6-di t-butyl phenol antioxidant, methylcyclopentadienyl manganese tricarbonyl combustion improver and octane enhancer, oleic acid plus N,N dimethylcyclohexylamine, dodecenyl succinic acid, polyisobutylene amine dispersant, 1,2 propane diamine salicylaldehyde metal deactivator, cresol Mannich dispersant, diethanol amide of isostearic acid friction modifier, and 2-ethyl hexyl nitrate combustion improver. The alkyl nitrate, 2-ethyl hexyl nitrate, was particularly effective in reducing deposits and hence improving the protection of a fuel delivery system in the engine combusting the E85 fuel blend.
  • Thus, there is provided herein a method of improving protection of a fuel delivery system in an internal combustion engine combusting an ethanol-gasoline blend, said method comprising combining the blend with at least one additive selected from the group consisting of 2,6-di t-butyl phenol antioxidant, methylcyclopentadienyl manganese tricarbonyl combustion improver and octane enhancer, oleic acid plus N,N dimethylcyclohexylamine, dodecenyl succinic acid, polyisobutylene amine dispersant, 1,2 propane diamine salicylaldehyde metal deactivator, cresol Mannich base dispersant, diethanol amide of isostearic acid friction modifier, and 2-ethyl hexyl nitrate combustion improver, whereby the deposits formed in said engine are less than the deposits formed in the engine when combusting the blend without the at least one additive.
  • In another example, a Keep Clean Test was performed by driving a Chevrolet Impala for 5,000 miles using fuel containing gasoline without ethanol, and fuel containing E85 blend. The Intake Valve Deposits (IVD) and the Combustion Chamber Deposits (CCD) were then measured and are reported in Table 3. The ethanol used in the E85 blend was ADM Ethanol except for Test No 6 where New Energy Ethanol was used.
  • TABLE 3
    Keep Clean Test 5000 Miles
    IVD, CCD,
    Test No. Ethanol % H-6560, PTB mg mg
    1 0 0 429 1232
    2 0 85  5 1438
    3 84  30/5 (1) 191 299
    4 74 85/22 (1) 134 265
    5 84 0 227 184
    6 84 0 99 176
    7 84   500 (2) 4 277
    (1) First number is treat rate in the gasoline, second number is treat rate in the finished blend.
    (2) H-6400 polyetheramine dispersant, not H-6560

    Table 3 illustrates the effect on deposits of having no ethanol (Test No's 1 and 2) when used without and with (respectively) HiTEC® 6560, a Mannich dispersant with a polyol and polyisobutylene carriers. The use of the dispersant reduced the IVD deposits from 429 mg to 5 mg. The E85 fuel blend of Test No. 3 at a 5 PTB treat rate of the Mannich dispersant in the finished fuel had a IVD deposit of 191 mg but when the dispersant was lacking from the E85 blend (Test No. 5), the IVD deposit went up to 227, due in part to the contribution from the ethanol. Comparing Test No. 3 and Test No. 4 also shows that reducing the ethanol content in the fuel blend from 84% to 74% reduced the deposits from 299 mg to 265 mg. This further illustrates that gasoline ethanol blends will need better dispersancy and detergency. Test No. 6 used the New Energy Ethanol which as shown in Table 1 contributes much less to deposits than does the ADM Ethanol, so the IVD in Table 3 correspondingly shows only 99 mg of deposit. Test No. 7 shows the result from a higher treat rate (500 PTB) of a polyetheramine dispersant and the result when combusting the E85 fuel was an amazingly low 4 mg of deposit, at least a major portion of which can be attributed to the ethanol by comparing to Test No. 6.
  • For the CCD results of Table 3, comparing Test No. 3 (E85 plus the Mannich dispersant) and Test No. 5 (E85 without the dispersant) one sees an improvement in reducing Combustion Chamber Deposits from 299 mg to 184 mg and using the cleaner New Energy Ethanol of Test No. 6 reduced the Combustion Chamber Deposit even further to 176 mg.
  • In this manner it is clear that the present disclosure provides a method to improve protection of a fuel delivery system in an engine combusting an ethanol-containing fuel by adding to the fuel a polyetheramine dispersant or a Mannich dispersant. It is therefore expected that the combination thereof will have similar or even enhanced and synergistic results. The reduction of deposit formation is directly related to increased longevity of the useful life of engine combustion surfaces, injectors, valves, gaskets, liners, seals, hoses, pumps, filters, and other fuel delivery system parts.
  • Example 1 Fuel Formulation with a Mannich Dispersant
  • A fuel composition is prepared by combining gasoline (15% by volume) and ethanol (85% by volume) and a Mannich base fuel additive (HiTEC® 6560 available from Afton Chemical Corporation, and having a PIB group with a MW of 950, and a cresol group reacted with dibutylamine). The fuel additive is present in the fuel composition at 200 ppm. The composition is fed to and combusted in a direct injection gasoline engine. The resulting fuel will demonstrate improved protection provided in the combustion engine and fuel delivery system compared to the protection resulting before and after combustion of a fuel composition not containing ethanol, as well as compared to the combustion of a fuel composition containing ethanol and gasoline but no Mannich base fuel additive.
  • Example 2 Fuel Formulation with a Succinimide Dispersant
  • A fuel composition is prepared by combining gasoline (15% by volume) and ethanol (85% by volume) and an alkylated succinimide dispersant (HiTEC® 4249 available from Afton Chemical Corporation, and having a PIB group with a MW of 950, and a maleic anhydride reacted with tetraethylene pentamine). The dispersant is present in the fuel composition at 100 ppm. The composition is fed to and combusted in a spark ignited internal combustion engine. The resulting fuel demonstrates improved protection in an internal combustion engine and its delivery system compared to the combustion of a fuel composition not containing ethanol, as well as compared to the combustion of a fuel composition containing ethanol and gasoline but no alkylated succinimide dispersant.
  • Example 3 Fuel Formulation with a Phenolic Antioxidant
  • A fuel composition is prepared by combining gasoline (15% by volume) and ethanol (85% by volume) and a phenolic driveability agent (HiTEC® 4733 available from Afton Chemical Corporation and containing 2,4 di-t-butyl phenol). The antioxidant is present in the fuel composition at 100 ppm. The composition is fed to and combusted in a gasoline engine. The resulting fuel improves protection in an internal combustion engine and its fuel delivery system compared to the combustion of a fuel composition not containing ethanol, as well as compared to the delivery and combustion of a fuel composition containing ethanol and gasoline but no phenolic antioxidant.
  • Example 4 Fuel Formulation with a Demulsifier
  • A fuel composition is prepared by combining gasoline (15% by volume) and ethanol (85% by volume) and a demulsifier agent (Baker Petrolite's Tolad 9372). The demulsifier agent is present in the fuel composition at 30 ppm. The composition is fed to and combusted in an internal combustion gasoline spark ignited engine. The resulting fuel improves the protection in an internal combustion engine and its fuel delivery system compared to the combustion and delivery of a fuel composition not containing ethanol, as well as compared to the combustion and delivery of a fuel composition containing ethanol and gasoline but no demulsifier.
  • Example 5 Fuel Formulation with a Dehazer
  • A fuel composition is prepared by combining gasoline (15% by volume) and ethanol (85% by volume) and a dehazer agent (2-ethyl hexanol available from BASF). The dehazer agent is present in the fuel composition at 5 weight percent. The composition is fed to and combusted in an internal combustion gasoline spark ignited engine. The resulting fuel improves protection in an internal combustion engine and its delivery system compared to the combustion and delivery of a fuel composition not containing ethanol, as well as compared to the combustion and delivery of a fuel composition containing ethanol and gasoline but no dehazer.
  • Example 6 Fuel Formulation with an Octane Improver
  • A fuel composition is prepared by combining gasoline (15% by volume) and ethanol (85% by volume) and a MMT octane improver (HiTEC® 3000 available from Afton Chemical Corporation). The octane improver is present in the fuel composition at 300 ppm. The composition is fed to and combusted in an internal combustion engine. The resulting fuel improves protection in an internal combustion engine and its delivery system compared to the combustion and delivery of a fuel composition not containing ethanol, as well as compared to the combustion and delivery of a fuel composition containing ethanol and gasoline but no MMT.
  • Example 7 Fuel Formulation with a Volatility Improver Agent
  • A fuel composition is prepared by combining gasoline (15% by volume) and ethanol (85% by volume) and a volatility improving agent (2-ethyl hexyl nitrate, HiTEC® 4103 available from Afton Chemical Corporation. The volatility improving agent is present in the fuel composition at 8 weight percent. The composition is fed to and combusted in a gasoline engine. The resulting fuel improves protection in an internal combustion engine and its delivery system compared to the combustion and delivery of a fuel composition not containing ethanol, as well as compared to the delivery and combustion of a fuel composition containing ethanol and gasoline but no volatility improving agent.
  • Example 8 Fuel Formulation with a Detergent
  • A fuel composition is prepared by combining gasoline (15% by volume) and ethanol (85% by volume) and a detergent agent (HiTEC® 611 available from Afton Chemical Corporation, and having an overbased calcium sulfonate). The detergent agent is present in the fuel composition at 2.5 weight percent. The composition is fed to and combusted in an internal combustion engine. The resulting fuel improves protection in an internal combustion engine and its delivery system compared to the delivery and combustion of a fuel composition not containing ethanol, as well as compared to the delivery and combustion of a fuel composition containing ethanol and gasoline but no detergent agent.
  • Other embodiments of the present disclosure will be apparent to those skilled in the art from consideration of the specification and practice of the disclosure disclosed herein. As used throughout the specification and claims, “a” and/or “an” may refer to one or more than one. Unless otherwise indicated, all numbers expressing quantities of ingredients, properties such as molecular weight, percent, ratio, reaction conditions, and so forth used in the specification and claims are to be understood as being modified in all instances by the term “about.” Accordingly, unless indicated to the contrary, the numerical parameters set forth in the specification and claims are approximations that may vary depending upon the desired properties sought to be obtained by the present disclosure. At the very least, and not as an attempt to limit the application of the doctrine of equivalents to the scope of the claims, each numerical parameter should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques. Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the disclosure are approximations, the numerical values set forth in the specific examples are reported as precisely as possible. Any numerical value, however, inherently contains certain errors necessarily resulting from the standard deviation found in their respective testing measurements. It is intended that the specification and examples be considered as exemplary only, with a true scope and spirit of the disclosure being indicated by the following claims.

Claims (21)

1. A method to improve protection of a fuel delivery system in an internal combustion engine, said method comprising delivering to or combusting in said engine a fuel composition comprising gasoline, ethanol and at least one fuel additive, said additive being selected from the group consisting succinimide dispersants, succinamide dispersants, amides, Mannich base dispersants, and polyetheramine dispersants.
2. The method of claim 1, wherein the fuel composition comprises at lease one second fuel additive, said additive being selected from the group consisting of phenolics, hindered phenolics, aryl amines, and diphenyl amines.
3. The method of claim 1, wherein the fuel composition comprises at lease one second fuel additive, said additive being selected from the group consisting of monocarboxylic acids, dicarboxylic acids, p-phenylenediamine and dicyclohexylamme.
4. The method of claim 1, wherein the fuel composition comprises at lease one second fuel additive, said additive being selected from the group consisting of oxylated alkylphenolic resins, and formaldehyde polymer with 4-( 1,1 -dimethylethyl)phenol, methyloxirane and oxirane.
5. The method of claim 1, wherein the fuel composition comprises at lease one second fuel additive, said additive being selected from the group consisting of methyl cyclopentadienyl manganese tricarbonyl, cyclopentadienyl manganese tricarbonyl, azides, tetraethyl lead, peroxides and alkyl nitrates.
6. The method of claim 1, wherein the fuel composition comprises at lease one second fuel additive, said additive being selected from the group consisting of monoesters, diesters, ethers, ketones, diethers, polyethers, glymes and glycols.
7. The method of claim 1, wherein the fuel composition comprises at lease one second fuel additive, said additive being selected from the group consisting of monocarboxylic acids, dicarboxylic acids, and polycarboxylic acids.
8. The method of claim 1, wherein the fuel composition comprises at lease one second fuel additive, said additive being selected from the group consisting of phenates, salicylates, sulfonates, nonylphenol ethoxylates, fuel-soluble alkali detergents and aikaline earth metal-containing detergents.
9. A fuel composition comprising gasoline, ethanol and at least one fuel delivery system protecting agent, said agent being selected from the group consisting of succinimide dispersants, succinamide dispersants, amides, Mannich base dispersants, polyetheramine dispersants, phenolics, hindered phenolics, aryl amines, diphenyl amines, monocarboxylic acids, dicarboxylic acids, polycarboxylic acids, p-phenylenediamine, dicyclohexylamine, oxylated alkylphenolic resins, formaidehyde polymer with 4-( 1,1 -dimethylethyl)phenol, methyloxirane and oxirane, methyl cyclopentadienyl manganese tricarbonyl, cyclopentadienyl manganese tricarbonyl, azides, tetraethyl lead, peroxides, alkyl nitrates, monoesters, diesters, ethers, dieters, ketones, polyethers, glycols, glymes, oxiranes, C1-C8 aliphatic hydrocarbons, butylene oxide, propylene oxide, ethylene oxide, epoxides, butane, pentane, xylene, nitrous oxide, nitromethane, phenates, salicylates, sulfonates, nonyiphenol ethoxylates, fuel-soluble alkali detergents and an alkaline earth metal-containing detergents.
10. A fuel composition consisting essentially of gasoline, ethanol and at least one fuel delivery system protecting agent, said agent being selected from the group consisting of succinimide dispersants, succinamide dispersants, amides, Mannich base dispersants, polyetheramine dispersants, phenolics, hindered phenolics, aryl amines, diphenyl amines, monocarboxylic acids, dicarboxylic acids, polycarboxylic acids, p-phenylenedianiine and dicyclohexylamine, oxylated alkylphenolic resins, formaldehyde polymer with 4-( 1,1 - dimethylethyl)phenol, methyloxirane and oxirane, methyl cyclopentadienyl manganese tricarbonyl, cyclopentadienyl manganese tricarbonyl, azides, tetraethyl lead, peroxides, alkyl nitrates, monoesters, diesters, ethers, dieters, polyethers, glycols, glymes, oxiranes, C1-C8 aliphatic hydrocarbons, butylene oxide, propylene oxide, ethylene oxide, epoxides, butane, pentane, xylene, nitrous oxide, nitromethane, phenates, salicylates, sulfonates, nonyiphenol ethoxylates, fuel-soluble alkali detergents and alkaline earth metal-containing detergents.
11. The composition of claim 9, wherein the ethanol content of the fuel composition is from about 74% to about 85%.
12. The composition of claim 9, wherein the ethanol content of the fuel composition is from about 50% to about 74%.
13. The composition of claim 10, wherein the ethanol content of the fuel composition is from about 74% to about 85%.
14. The composition of claim 10, wherein the ethanol content of the fuel composition is from about 50% to about 74%.
15. A method of improving the protection of an engine combusting a fuel composition containing gasoline and ethanol, said method consisting essentially of combining the fuel and an additive selected from the group consisting of monoesters, diesters, ethers, ketones, diethers, polyethers, glymes and glycols, wherein the protection of said engine is improved relative to the protection of the engine combusting a gasoline fuel without ethanol.
16. A method of improving the protection of an engine combusting a fuel composition containing gasoline and ethanol, said method comprising combining the fuel and an additive selected from the group consisting of succinimide dispersants, succinamide dispersants, amides, Mannich base dispersants, polycteramine dispersants, phenolics, hindered phenolics, aryl amines, diphenyl amines, monocarboxylic acids, dicarboxylic acids, polycarboxylic acids, p- phenylenediamine and dicyclohexylamine, oxylated alkylphenolic resins, formaldehyde polymer with 4-( 1,1 -dimethylethyl)phenol, methyloxirane and oxirane, methyl cyclopentadienyl manganese tricarbonyl, cyclopentadienyl manganese tricarbonyl, azides, tetraethyl lead, peroxides, alkyl nitrates, monoesters, diesters, ethers, ketones, diethers, polyethers, glycols, glymes, oxiranes, C1-C8 aliphatic hydrocarbons, butylene oxide, propylene oxide, ethylene oxide, epoxides, butane, pentane, xylene, nitrous oxide, nitromethane, phenates, salicylates, sulfonates, nonyiphenol ethoxylates, thel-soluble alkali detergents and alkaline earth metal- containing detergents, wherein the protection of said engine is improved relative to the protection of the engine combusting a gasoline fuel without ethanol.
17. The method of claim 3, wherein the monocarboxylic acid is a tall oil fatty acid.
18. The method of claim 3, wherein the dicarboxylic acid is dodecenyl succinic acid.
19. The method of claim 16, wherein the monocarboxylic acid is a tall oil fatty acid.
20. The method of claim 16, wherein the dicarboxylic acid is dodecenyl succinic acid.
21. A fuel delivery system protecting agent concentrate for gasoline engines combusting an ethanol-containing fuel, said concentrate comprising one or more fuel delivery system protecting agents and a diluent selected from the group consisting of an oil, a fuel, gasoline, ethanol, solvent, carrier fluid, and other liquid materials combustible in a gasoline engine.
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20130291429A1 (en) * 2010-10-14 2013-11-07 Kyoritsu Plastic Seisakusho Additive for water-added bio fuel, water-added bio fuel, and method of producing the same
CN104371768A (en) * 2014-11-13 2015-02-25 山东华亚环保科技有限公司 High-cleanliness alcohol gasoline and preparation method thereof
CN111117741A (en) * 2019-12-24 2020-05-08 江苏创新石化有限公司 Gasoline and diesel direct injection engine cleaning lubricant and preparation method thereof

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102159686B (en) * 2008-09-16 2014-07-30 卢布里佐尔公司 Alcohol fuel soluble additive for removing deposits in fueling systems

Citations (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4242099A (en) * 1979-02-09 1980-12-30 Ethyl Corporation Fuel additive for diesel fuels
US4282008A (en) * 1980-09-22 1981-08-04 Texaco Inc. Novel fuel composition containing alcohol
US4282007A (en) * 1980-09-22 1981-08-04 Texaco Inc. Novel fuel composition containing alcohol
US4294585A (en) * 1980-09-22 1981-10-13 Texaco Inc. Novel fuel composition for internal combustion engine
US4328003A (en) * 1979-08-06 1982-05-04 Exxon Research & Engineering Co. Alcohol fuels of decreased corrosivity
US4365972A (en) * 1981-11-05 1982-12-28 Texaco Inc. Fuel composition
US4371377A (en) * 1980-11-26 1983-02-01 Adriel Energy Corporation Fuel additive
US4376635A (en) * 1980-09-22 1983-03-15 Texaco Inc. Novel gasohol or ethanol fuel composition containing as a corrosion inhibitor the reaction product of benzothiazole, formaldehyde and an N-alkyl propylene diamine
US4376636A (en) * 1981-11-18 1983-03-15 Adriel Energy Corporation Fuel additive
US4385904A (en) * 1982-02-01 1983-05-31 Texaco Inc. Novel corrosion inhibitor for alcohol fuels
US4391610A (en) * 1982-01-08 1983-07-05 Texaco Inc. Liquid hydrocarbon fuel containing a corrosion inhibitor, dialkoxylated alkyl polyoxyalkyl primary amine
US4398921A (en) * 1981-11-02 1983-08-16 Ethyl Corporation Gasohol compositions
US4412667A (en) * 1981-02-12 1983-11-01 Frank Doerner Leg for chair base and cap therefore
US4426208A (en) * 1981-11-02 1984-01-17 Ethyl Corporation Corrosion inhibitors for alcohol-based fuels
US4428754A (en) * 1982-03-01 1984-01-31 The Dow Chemical Company N, N-Bis (hydroxyalkyl) alkyl amides as phase separation inhibitors in liquid hydrocarbon and ethanol mixtures
US4435186A (en) * 1982-05-03 1984-03-06 Texaco Inc. Alcohol fuels containing wear-inhibiting amounts of reaction products of amines and phosphate esters of phosphonic acids
US4440545A (en) * 1981-11-02 1984-04-03 Ethyl Corporation Gasohol having corrosion inhibiting properties
US4504279A (en) * 1984-07-09 1985-03-12 Texaco Inc Corrosion inhibited motor fuel
US4504278A (en) * 1984-06-27 1985-03-12 Texaco Inc. Corrosion inhibited motor fuel
US4505717A (en) * 1984-06-25 1985-03-19 Texaco Inc. Corrosion inhibited motor fuel
US4530802A (en) * 1981-11-05 1985-07-23 Texaco Inc. Di-hydrocarbyl phosphate quaternary amine salts with an amide of an amino carboxylic acid
US4531948A (en) * 1984-06-13 1985-07-30 Ethyl Corporation Alcohol and gasohol fuels having corrosion inhibiting properties
US4536189A (en) * 1984-04-27 1985-08-20 Texaco Inc. Corrosion inhibitor and motor fuel composition containing the same
US4549882A (en) * 1984-10-19 1985-10-29 Ethyl Corporation Corrosion inhibitors for alcohol containing fuels
US4609377A (en) * 1985-10-07 1986-09-02 Texaco Inc. Aminated polyisopropoxylated polyethoxylated alkylphenol and ethanol/gasoline blend composition containing same
US4610696A (en) * 1984-07-03 1986-09-09 Elf France Process for the formation of homogeneous fuel compositions containing a petroleum cut and at least one short chain aliphatic alcohol and compositions thereby obtained
US4668245A (en) * 1986-10-22 1987-05-26 Bankamerica Corporation Fuel additive for use in alcohol fuels
US4737159A (en) * 1984-06-29 1988-04-12 E. I. Du Pont De Nemours And Company Corrosion inhibitor for liquid fuels
US4801305A (en) * 1983-03-10 1989-01-31 Union Rheinische Braunkohlen Kraftstoff Ag Motor-fuels
US4806129A (en) * 1987-09-21 1989-02-21 Prepolene Industries, Inc. Fuel extender
US5679116A (en) * 1992-05-06 1997-10-21 Ethyl Corporation Compositions for control of induction system deposits
US5725612A (en) * 1996-06-07 1998-03-10 Ethyl Corporation Additives for minimizing intake valve deposits, and their use
US6017369A (en) * 1998-11-23 2000-01-25 Pure Energy Corporation Diesel fuel composition
US6048373A (en) * 1998-11-30 2000-04-11 Ethyl Corporation Fuels compositions containing polybutenes of narrow molecular weight distribution
US6129773A (en) * 1993-07-16 2000-10-10 Killick; Robert William Fuel blends
US6420791B1 (en) * 1999-11-23 2002-07-16 United Microelectronics Corp. Alignment mark design
US20030029077A1 (en) * 2001-08-07 2003-02-13 The Lubrizol Corporation, A Corporation Of The State Of Ohio Fuel composition containing detergent combination and methods thereof
US6761745B2 (en) * 2000-01-24 2004-07-13 Angelica Hull Method of reducing the vapor pressure of ethanol-containing motor fuels for spark ignition combustion engines
US6835217B1 (en) * 2000-09-20 2004-12-28 Texaco, Inc. Fuel composition containing friction modifier
US20050028435A1 (en) * 1999-11-19 2005-02-10 Stuart Pace Low nitrogen content fuel with improved lubricity
US20050034360A1 (en) * 2003-08-13 2005-02-17 Aradi Allen A. Use of detergent additives in high-ethanol fuels for deposit control
US20050089685A1 (en) * 2003-08-11 2005-04-28 Nissan Motor Co., Ltd. Fuel lubricated sliding mechanism
US6949462B1 (en) * 2002-04-04 2005-09-27 Nanometrics Incorporated Measuring an alignment target with multiple polarization states
US7046361B1 (en) * 2002-04-04 2006-05-16 Nanometrics Incorporated Positioning two elements using an alignment target with a designed offset
US20060168877A1 (en) * 2005-01-31 2006-08-03 Leonid Shvartsman Anti-detonation additive, and fuel provided therewith
US20060196111A1 (en) * 2005-03-04 2006-09-07 Colucci William J Fuel additive composition
US20060196110A1 (en) * 2003-04-11 2006-09-07 Basf Aktiengesellschaft Fuel composition

Patent Citations (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4242099A (en) * 1979-02-09 1980-12-30 Ethyl Corporation Fuel additive for diesel fuels
US4328003A (en) * 1979-08-06 1982-05-04 Exxon Research & Engineering Co. Alcohol fuels of decreased corrosivity
US4376635A (en) * 1980-09-22 1983-03-15 Texaco Inc. Novel gasohol or ethanol fuel composition containing as a corrosion inhibitor the reaction product of benzothiazole, formaldehyde and an N-alkyl propylene diamine
US4282008A (en) * 1980-09-22 1981-08-04 Texaco Inc. Novel fuel composition containing alcohol
US4282007A (en) * 1980-09-22 1981-08-04 Texaco Inc. Novel fuel composition containing alcohol
US4294585A (en) * 1980-09-22 1981-10-13 Texaco Inc. Novel fuel composition for internal combustion engine
US4371377A (en) * 1980-11-26 1983-02-01 Adriel Energy Corporation Fuel additive
US4412667A (en) * 1981-02-12 1983-11-01 Frank Doerner Leg for chair base and cap therefore
US4398921A (en) * 1981-11-02 1983-08-16 Ethyl Corporation Gasohol compositions
US4426208A (en) * 1981-11-02 1984-01-17 Ethyl Corporation Corrosion inhibitors for alcohol-based fuels
US4440545A (en) * 1981-11-02 1984-04-03 Ethyl Corporation Gasohol having corrosion inhibiting properties
US4530802A (en) * 1981-11-05 1985-07-23 Texaco Inc. Di-hydrocarbyl phosphate quaternary amine salts with an amide of an amino carboxylic acid
US4365972A (en) * 1981-11-05 1982-12-28 Texaco Inc. Fuel composition
US4376636A (en) * 1981-11-18 1983-03-15 Adriel Energy Corporation Fuel additive
US4391610A (en) * 1982-01-08 1983-07-05 Texaco Inc. Liquid hydrocarbon fuel containing a corrosion inhibitor, dialkoxylated alkyl polyoxyalkyl primary amine
US4385904A (en) * 1982-02-01 1983-05-31 Texaco Inc. Novel corrosion inhibitor for alcohol fuels
US4428754A (en) * 1982-03-01 1984-01-31 The Dow Chemical Company N, N-Bis (hydroxyalkyl) alkyl amides as phase separation inhibitors in liquid hydrocarbon and ethanol mixtures
US4435186A (en) * 1982-05-03 1984-03-06 Texaco Inc. Alcohol fuels containing wear-inhibiting amounts of reaction products of amines and phosphate esters of phosphonic acids
US4801305A (en) * 1983-03-10 1989-01-31 Union Rheinische Braunkohlen Kraftstoff Ag Motor-fuels
US4536189A (en) * 1984-04-27 1985-08-20 Texaco Inc. Corrosion inhibitor and motor fuel composition containing the same
US4531948A (en) * 1984-06-13 1985-07-30 Ethyl Corporation Alcohol and gasohol fuels having corrosion inhibiting properties
US4505717A (en) * 1984-06-25 1985-03-19 Texaco Inc. Corrosion inhibited motor fuel
US4504278A (en) * 1984-06-27 1985-03-12 Texaco Inc. Corrosion inhibited motor fuel
US4737159A (en) * 1984-06-29 1988-04-12 E. I. Du Pont De Nemours And Company Corrosion inhibitor for liquid fuels
US4610696A (en) * 1984-07-03 1986-09-09 Elf France Process for the formation of homogeneous fuel compositions containing a petroleum cut and at least one short chain aliphatic alcohol and compositions thereby obtained
US4504279A (en) * 1984-07-09 1985-03-12 Texaco Inc Corrosion inhibited motor fuel
US4549882A (en) * 1984-10-19 1985-10-29 Ethyl Corporation Corrosion inhibitors for alcohol containing fuels
US4609377A (en) * 1985-10-07 1986-09-02 Texaco Inc. Aminated polyisopropoxylated polyethoxylated alkylphenol and ethanol/gasoline blend composition containing same
US4668245A (en) * 1986-10-22 1987-05-26 Bankamerica Corporation Fuel additive for use in alcohol fuels
US4806129A (en) * 1987-09-21 1989-02-21 Prepolene Industries, Inc. Fuel extender
US5679116A (en) * 1992-05-06 1997-10-21 Ethyl Corporation Compositions for control of induction system deposits
US6129773A (en) * 1993-07-16 2000-10-10 Killick; Robert William Fuel blends
US5725612A (en) * 1996-06-07 1998-03-10 Ethyl Corporation Additives for minimizing intake valve deposits, and their use
US6017369A (en) * 1998-11-23 2000-01-25 Pure Energy Corporation Diesel fuel composition
US6048373A (en) * 1998-11-30 2000-04-11 Ethyl Corporation Fuels compositions containing polybutenes of narrow molecular weight distribution
US20050028435A1 (en) * 1999-11-19 2005-02-10 Stuart Pace Low nitrogen content fuel with improved lubricity
US6420791B1 (en) * 1999-11-23 2002-07-16 United Microelectronics Corp. Alignment mark design
US6761745B2 (en) * 2000-01-24 2004-07-13 Angelica Hull Method of reducing the vapor pressure of ethanol-containing motor fuels for spark ignition combustion engines
US6835217B1 (en) * 2000-09-20 2004-12-28 Texaco, Inc. Fuel composition containing friction modifier
US20030029077A1 (en) * 2001-08-07 2003-02-13 The Lubrizol Corporation, A Corporation Of The State Of Ohio Fuel composition containing detergent combination and methods thereof
US7046361B1 (en) * 2002-04-04 2006-05-16 Nanometrics Incorporated Positioning two elements using an alignment target with a designed offset
US6949462B1 (en) * 2002-04-04 2005-09-27 Nanometrics Incorporated Measuring an alignment target with multiple polarization states
US20060196110A1 (en) * 2003-04-11 2006-09-07 Basf Aktiengesellschaft Fuel composition
US20050089685A1 (en) * 2003-08-11 2005-04-28 Nissan Motor Co., Ltd. Fuel lubricated sliding mechanism
US20050034360A1 (en) * 2003-08-13 2005-02-17 Aradi Allen A. Use of detergent additives in high-ethanol fuels for deposit control
US20060168877A1 (en) * 2005-01-31 2006-08-03 Leonid Shvartsman Anti-detonation additive, and fuel provided therewith
US20060196111A1 (en) * 2005-03-04 2006-09-07 Colucci William J Fuel additive composition

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20130291429A1 (en) * 2010-10-14 2013-11-07 Kyoritsu Plastic Seisakusho Additive for water-added bio fuel, water-added bio fuel, and method of producing the same
CN104371768A (en) * 2014-11-13 2015-02-25 山东华亚环保科技有限公司 High-cleanliness alcohol gasoline and preparation method thereof
CN111117741A (en) * 2019-12-24 2020-05-08 江苏创新石化有限公司 Gasoline and diesel direct injection engine cleaning lubricant and preparation method thereof

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