US20040093790A1 - Combustion improvers for normally liquid fuels - Google Patents

Combustion improvers for normally liquid fuels Download PDF

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Publication number
US20040093790A1
US20040093790A1 US10/468,745 US46874503A US2004093790A1 US 20040093790 A1 US20040093790 A1 US 20040093790A1 US 46874503 A US46874503 A US 46874503A US 2004093790 A1 US2004093790 A1 US 2004093790A1
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Prior art keywords
fuel
fuel composition
group
hydroxylamine
independently
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US10/468,745
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Mark Baker
Douglas Barr
Daniel Daly
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Lubrizol Corp
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Lubrizol Corp
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Priority to US10/468,745 priority Critical patent/US20040093790A1/en
Priority claimed from PCT/US2002/005990 external-priority patent/WO2002068570A2/en
Assigned to THE LUBRIZOL CORPORATION reassignment THE LUBRIZOL CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: DALY, DANIEL T., BAKER, MARK R.
Assigned to LUBRIZOL CORPORATION, THE reassignment LUBRIZOL CORPORATION, THE ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: BARR, DOUGLAS M.
Publication of US20040093790A1 publication Critical patent/US20040093790A1/en
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Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • 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
    • C10L10/00Use of additives to fuels or fires for particular purposes
    • C10L10/02Use of additives to fuels or fires for particular purposes for reducing smoke development
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • 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
    • C10L1/103Liquid carbonaceous fuels containing additives stabilisation of anti-knock agents
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • 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
    • C10L1/14Organic compounds
    • C10L1/22Organic compounds containing nitrogen
    • C10L1/222Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
    • C10L1/2222(cyclo)aliphatic amines; polyamines (no macromolecular substituent 30C); quaternair ammonium compounds; carbamates
    • C10L1/2225(cyclo)aliphatic amines; polyamines (no macromolecular substituent 30C); quaternair ammonium compounds; carbamates hydroxy containing
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • 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
    • C10L1/12Inorganic compounds
    • C10L1/1233Inorganic compounds oxygen containing compounds, e.g. oxides, hydroxides, acids and salts thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • 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
    • C10L1/12Inorganic compounds
    • C10L1/1266Inorganic compounds nitrogen containing compounds, (e.g. NH3)
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • 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
    • C10L1/12Inorganic compounds
    • C10L1/1275Inorganic compounds sulfur, tellurium, selenium containing compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • 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
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • 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
    • C10L1/1824Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms mono-hydroxy
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • 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
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/185Ethers; Acetals; Ketals; Aldehydes; Ketones
    • C10L1/1852Ethers; Acetals; Ketals; Orthoesters
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • 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
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/188Carboxylic acids; metal salts thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • 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
    • C10L1/14Organic compounds
    • C10L1/22Organic compounds containing nitrogen
    • C10L1/222Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
    • C10L1/224Amides; Imides carboxylic acid amides, imides

Definitions

  • This invention relates to combustion improving additives for normally liquid fuels.
  • driveability Overall performance of a vehicle is known as ‘driveability’.
  • ‘driveability’ of a vehicle has been defined as the degree to which a vehicle starts readily, idles evenly, drives smoothly when cruising and accelerating, and generally responds to the throttle. Ambient temperatures during which a vehicle is operated have an effect on driveability. Driveability is also affected by fuel-air mixture ratio and by emission controls. Some lower grade fuels can adversely affect driveability.
  • K. Owen and T. Coley “Automotive Fuels Reference Book”, Second Edition, Society of Automotive Engineers (Pub.), 1995, pp 173-181.
  • Combustion improvers of this invention improve combustion characteristics of fuels.
  • the improved combustion characteristics include reduced particulate emissions, reduced CO emissions, reduced NO x emissions, reduced hydrocarbon emissions, greater power output, reduced misfiring and improved fuel efficiency.
  • U.S. Pat. No. 2,314,137 describes organic hydroxylamines as a class of compounds which, when added in minor proportions to Diesel fuel, are effective to decrease the ignition delay period and thereby improve the ignition quality of the fuel and the consequent operation of the engine in which it is used.
  • U.S. Pat. No. 4,670,131 relates to fouling of equipment used for processing of organic feed streams containing olefinic compounds controlled by inhibiting polymerization of the olefinic compounds by carrying out the processing in the presence of from about 20 ppb to less than 1,000 ppb of a stable free radical, such as nitroxide.
  • U.S. Pat. No. 5,460,634 describes an additive package comprising an oil-soluble, stable free radical, such as a nitroxide, or a precursor therefor, used in a fuel oil to reduce, on combustion of the fuel oil, one or more of particulate emissions, hydrocarbon emissions, carbon monoxide emissions, and oxides of nitrogen emissions.
  • an oil-soluble, stable free radical such as a nitroxide, or a precursor therefor
  • U.S. Pat. No. 5,525,127 relates to hydrocarbonaceous distillate fuel compositions and additive concentrates are described as providing improved performance in evaporative burners.
  • the additive components comprise a mixture formed that at least (a) a cyclopentadienyl manganese tricarbonyl compound; (b) a succinic derivative ashless dispersant; (c) an aliphatic dicarboxylic acid having at least 24 carbon atoms in the molecule, the two carboxyl groups being separated from each other by at least 6 carbon atoms; and (d) a metal deactivator of the chelation type.
  • the compositions also contain (e) alkoxylated alkylphenol; (f) a demulsifying agent; (g) a tertiary monoamine in which each substituent on the nitrogen atom is a hydrocarbyl group; and (h) liquid inert solvent having a final boiling point no higher than approximately 600° C.
  • the compositions are devoid of any metal-containing additive component other than the cyclopentadienyl manganese tricarbonyl compound.
  • U.S. Pat. No. 5,529,706 describes tolyltriazole derived esters of tri, tetra, and poly carboxylic acids or an acid generating compound which are effective lubricity additives for lube oils, greases, or distillate fuels.
  • U.S. Pat. No. 5,578,556 relates to triazole-dialkyl maleate derivatives which are described as effective metal passivators and antiwear additives for lubricants and fuels.
  • U.S. Pat. No. 5,591,237 describes a fuel additive concentrate package comprising a detergent/dispersant, an organic nitrate combustion improver, and a corrosion inhibitor comprising dimer and/or trimer acid to provide enhanced shelf life stability by treating the concentrate with a shelf life stability amount, for example 1,500 and 10,000 ppm, respectively of acid selected from the group consisting of nitric acid/hydrochloric acid.
  • U.S. Pat. No. 5,669,938 describes a fuel composition which comprises a water-in-oil emulsion comprising a major proportion of a hydrocarbonaceous middle distillate fuel and about 1 to about 40 volume percent water, and an emission reducing amount of at least one fuel-soluble organic nitrate ignition improver such as 2-ethylhexyl nitrate providing reduction of exhaust emissions from diesel engines.
  • U.S. Pat. No. 5,782,937 relates to fuel compositions containing hydrocarbon fuels in the gasoline boiling range and organic nitrogen-containing compounds selected from organic nitrates and/or organic nitro compounds.
  • the fuel compositions exhibit improved ignition properties, including reduced emissions and reduced misfires.
  • U.S. Pat. No. 5,944,858 relates to hydrocarbonaceous fuels and additive compositions therefor which comprise: a) one or more fuel-soluble manganese carbonyl compounds; and b) one or more fuel soluble alkali or alkaline earth metal containing neutral or basic detergent salts and preferably, also contain c) one or more of fuel-soluble ashless dispersants; d) at least one fuel soluble demulsifying agent; e) at least one aliphatic or cycloaliphatic amine; and f) at least one metal deactivator.
  • the fuel compositions are said to possess improved combustion characteristics.
  • U.S. Pat. No. 5,928,392 describes a burner operated by continuously feeding into its combustion zone while combustion is occurring therein, (a) a middle distillate burner fuel with which has been blended a minor combustion improving amount of manganese polycarbonyl compound and a total amount of air above 100% of the stoichiometric amount required for complete combustion of all fuel being introduced into said zone but which is below 105% of such stoichiometric amount.
  • a middle distillate burner fuel with which has been blended a minor combustion improving amount of manganese polycarbonyl compound and a total amount of air above 100% of the stoichiometric amount required for complete combustion of all fuel being introduced into said zone but which is below 105% of such stoichiometric amount.
  • alkali or alkaline earth metal containing detergent and fuel soluble dispersant have been blended into the fuel.
  • European Patent EP 0420581A1 describes an additive for hydrocarbon fuels which includes ethanolamine nitrate as an additive to reduce the quantity of smoke and improve the efficiency of combustion. Fuels are improved by the addition of the additive, which can be prepared by the reaction of ammonium nitrate and anhydrous ethanol in the presence of one or more nitro compounds of formula
  • R is a hydrogen atom or a C 1-4 alkyl radical, at a temperature of not more than 40-45° C., the nitro derivative being applied in a concentration of 1 to 3% by weight, the molar ratio between the nitro compound(s) and the ammonium nitrate being at least 0.05:1.
  • the instant invention is directed to fuel compositions comprising a major amount of a normally liquid hydrocarbon based fuel and a minor amount of a hydroxylamine or a salt thereof. More often, each hydroxylamino group of the hydroxylamine or salt thereof contains no more than one tertiary alkyl substituent.
  • the hydroxylamine or salt thereof provides improved combustion properties to a wide variety of normally liquid hydrocarbon based fuels, including fuels such as hydrocarbon fuels, biomass fuels and oxygenates.
  • the invention also is directed to a method for improving the combustion characteristics of a normally liquid hydrocarbon based fuel comprising incorporating therein a combustion improving amount of a hydroxylamine or a salt thereof.
  • hydrocarbyl or “hydrocarbon based” mean that the group being described has predominantly hydrocarbon character within the context of this invention. These include groups that are purely hydrocarbon in nature, that is, they contain only carbon and hydrogen. They may also include groups containing substituents or atoms which do not alter the predominantly hydrocarbon character of the group. Such substituents may include halo-, alkoxy-, nitro-, hydroxyl, etc. These groups also may contain hetero atoms. Suitable hetero atoms will be apparent to those skilled in the art and include, for example, sulfur, nitrogen and oxygen. Therefore, while remaining predominantly hydrocarbon in character within the context of this invention, these groups may contain atoms other than carbon present in a chain or ring otherwise composed of carbon atoms.
  • the fuel compositions of this invention comprise at least one hydroxylamine or a salt thereof. More often, each hydroxylamino group of the hydroxylamine or salt thereof contains no more than one tertiary alkyl substituent.
  • the hydroxylamine has the general formula
  • each of R a and R b is, independently, a member selected from the group consisting of H, a primary hydrocarbyl group and a secondary hydrocarbyl group, particularly, H or a hydrocarbyl group containing from 1 to about 25 carbon atoms, and especially a lower alkyl group, and n ranges from 1 to about 30, preferably, from 1 to about 4, and most preferably, 1.
  • R a is H
  • n equals 1.
  • each hydrocarbyl group is, independently, a primary alkyl group, especially one containing from 1 to about 6 carbon atoms.
  • the hydroxylamine has the general formula
  • each R c is, independently, H or a hydrocarbyl group, particularly, H or a lower alkyl group
  • each R d is, independently, a lower alkylene group, preferably an ethylene or propylene group, most preferably, an ethylene group
  • x ranges from 1 to about 29, preferably, from 1 to about 5.
  • the fuel composition comprises a hydroxylamine salt.
  • Hydroxylamines from which the hydroxylamine salts are derived are the same as the hydroxylamines described hereinabove.
  • the salt is at least one member of the group consisting of nitrates, sulfates, sulfonates, carbonates and carboxylates. Nitrates and carbonates are preferred with nitrates being particularly preferred.
  • the salts are generally obtained by contacting a hydroxylamine with an appropriate acid, optionally, in the presence of a diluent. Many of these salts are commercially available, for example, from chemical supply houses such as Aldrich Chemical Company, Milwaukee, Wis., USA.
  • the fuels of this invention include all normally liquid hydrocarbon based fuels known in the art.
  • normally liquid is meant a fuel which is liquid or liquefiable at normal operating temperatures.
  • hydrocarbon based means the fuel contains hydrocarbon moieties.
  • gasoline meeting ASTM Specification D-4814, diesel fuel meeting ASTM Specification D-975, heating oil meeting ASTM Specification D-396, oxygenates, mixtures of predominantly hydrocarbon fuels and oxygenates, biomass fuel and synthetic fuels.
  • Hydrocarbon based fuels are those fuels that contain hydrocarbon groups, and especially those that are substantially hydrocarbon, that is, those fuels derived from mineral oil sources, for example, gasoline and middle distillate oils, diesel oil and heating oils, synthetic hydrocarbon fuels such as polyolefins, alkylated aromatic hydrocarbon group containing fuels, hydrocarbon fuels obtained by the Fischer-Tropsch process, and others.
  • Mixtures of hydrocarbon based fuels and oxygenates include mixtures of any of the aforementioned hydrocarbon based fuels with any of alkanols, especially lower alkanols, and ethers, for example, methyl-t-butyl ether, methyl-t-amyl ether, dimethoxymethane and diethoxymethane, and particularly, lower alkanols such as ethanol.
  • Biomass fuels are derived from organic materials, such as seeds. Processes for obtaining these oils from biomass are described in numerous U.S. Patents, many of which are listed in U.S. Pat. No. 6,166,231 which is hereby incorporated herein by reference for relevant disclosures of such oils and methods for obtaining them.
  • biomass fuels are vegetable oil, for example, sunflower oil and rapeseed oils.
  • the fuel compositions of this invention comprise a minor amount of hydroxylamine or salt thereof. More typically, the fuel compositions comprise from about 50 to about 50,000 parts by weight, even more often from about 1,000 to about 10,000 or to about 5,000 parts by weight, hydroxylamine or salt thereof per million parts by weight of fuel.
  • the fuel compositions of the present invention may contain other additives which are well known to those skilled in the art. These can include combustion modifiers, such as octane number enhancers for gasoline, for example, anti-knock agents such as tetra-alkyl lead compounds and certain ethers, cetane number improvers for diesel fuels such as alkyl nitrates, lead scavengers such as halo-alkanes, dyes, antioxidants such as hindered phenols, lubricity agents, cold flow improvers, dispersants, surfactants, rust inhibitors such as alkylated succinic acids and anhydrides and derivatives thereof, bacteriostatic agents, auxiliary dispersants and detergents, gum inhibitors, fluidizers, metal deactivators, demulsifiers, anti-icing agents and the like.
  • the fuel compositions of this invention may be lead-containing or lead-free fuels. Preferred are lead-free fuels.
  • a fuel composition is prepared by mixing together, at high speed, 85 parts of a low sulfur No. 2 fuel oil, 15 parts anhydrous ethanol and 0.5 parts N,N-diethylhydroxylamine.
  • a fuel composition is prepared by mixing together 100 parts of a low sulfur No. 2 fuel oil and 0.5 parts N,N-diethylhydroxylamine.
  • a fuel composition contains 95 parts unleaded gasoline and 5 parts methanol emulsified with 1.0 part of a 1:1 by weight mixture of a polyether amine prepared by reductive cyanoethylation of C 12-15 substituted polyoxypropylene monool and a N,N-diethylhydroxylamine hexadecyl substituted succinic ester-salt prepared by reacting one mole each of hexadecyl substituted succinic anhydride with dimethylethanolamine to which emulsion is added 0.5 part N,N-diethylhydroxylamine.
  • a polyether amine prepared by reductive cyanoethylation of C 12-15 substituted polyoxypropylene monool
  • a N,N-diethylhydroxylamine hexadecyl substituted succinic ester-salt prepared by reacting one mole each of hexadecyl substituted succinic anhydride with dimethylethanolamine to which emulsion is
  • a fuel composition contains 96.33 parts diesel fuel, 1.0 parts C 12-15 alkyl poly(oxypropyl) 24 propyl amine, 1 part hexadecenyl succinic dimethylaminoethyl ester-salt and 1.67 parts 13M aqueous hydroxylammonium nitrate.
  • a fuel composition contains 99.50 parts gasoline and 0.5 part N,N-diethylhydroxylamine.

Abstract

Fuel compositions comprising a major amount of a normally liquid fuel and a minor amount of a hydroxylamine or a salt thereof, more often wherein each hydroxylamino group of the hydroxylamine or salt thereof contains no more than one tertiary alkyl substituent. The hydroxylamine or salt thereof provide improved combustion properties to a wide variety of normally liquid fuels, including hydrocarbon based fuels, oxygenates and synthetic fuels.

Description

    RELATED APPLICATIONS
  • This application claims priority from U.S. Provisional Application Serial No. 60/272,209, filed Feb. 28, 2001.[0001]
  • FIELD OF THE INVENTION
  • This invention relates to combustion improving additives for normally liquid fuels. [0002]
  • BACKGROUND OF THE INVENTION
  • The industry has continued to search for ways to improve combustion of normally liquid fuels. These include fuels used in heating systems, internal combustion engines and the like. Government agencies have imposed regulations requiring continuing reduction of emissions resulting from the combustion of fuels. Improved fuel economy is also required, not only by government regulations but also by consumers facing increased costs for fuels. Improved combustion of fuels generally results in a reduction in harmful emissions and more efficient utilization of fuels resulting in greater fuel economy. [0003]
  • Overall performance of a vehicle is known as ‘driveability’. Specifically, ‘driveability’ of a vehicle has been defined as the degree to which a vehicle starts readily, idles evenly, drives smoothly when cruising and accelerating, and generally responds to the throttle. Ambient temperatures during which a vehicle is operated have an effect on driveability. Driveability is also affected by fuel-air mixture ratio and by emission controls. Some lower grade fuels can adversely affect driveability. A discussion of driveability appears in K. Owen and T. Coley, “Automotive Fuels Reference Book”, Second Edition, Society of Automotive Engineers (Pub.), 1995, pp 173-181. [0004]
  • Combustion improvers of this invention improve combustion characteristics of fuels. The improved combustion characteristics include reduced particulate emissions, reduced CO emissions, reduced NO[0005] x emissions, reduced hydrocarbon emissions, greater power output, reduced misfiring and improved fuel efficiency.
  • U.S. Pat. No. 2,314,137 describes organic hydroxylamines as a class of compounds which, when added in minor proportions to Diesel fuel, are effective to decrease the ignition delay period and thereby improve the ignition quality of the fuel and the consequent operation of the engine in which it is used. [0006]
  • U.S. Pat. No. 4,670,131 relates to fouling of equipment used for processing of organic feed streams containing olefinic compounds controlled by inhibiting polymerization of the olefinic compounds by carrying out the processing in the presence of from about 20 ppb to less than 1,000 ppb of a stable free radical, such as nitroxide. [0007]
  • U.S. Pat. No. 5,460,634 describes an additive package comprising an oil-soluble, stable free radical, such as a nitroxide, or a precursor therefor, used in a fuel oil to reduce, on combustion of the fuel oil, one or more of particulate emissions, hydrocarbon emissions, carbon monoxide emissions, and oxides of nitrogen emissions. [0008]
  • U.S. Pat. No. 5,525,127 relates to hydrocarbonaceous distillate fuel compositions and additive concentrates are described as providing improved performance in evaporative burners. The additive components comprise a mixture formed that at least (a) a cyclopentadienyl manganese tricarbonyl compound; (b) a succinic derivative ashless dispersant; (c) an aliphatic dicarboxylic acid having at least 24 carbon atoms in the molecule, the two carboxyl groups being separated from each other by at least 6 carbon atoms; and (d) a metal deactivator of the chelation type. Preferably, the compositions also contain (e) alkoxylated alkylphenol; (f) a demulsifying agent; (g) a tertiary monoamine in which each substituent on the nitrogen atom is a hydrocarbyl group; and (h) liquid inert solvent having a final boiling point no higher than approximately 600° C. The compositions are devoid of any metal-containing additive component other than the cyclopentadienyl manganese tricarbonyl compound. [0009]
  • U.S. Pat. No. 5,529,706 describes tolyltriazole derived esters of tri, tetra, and poly carboxylic acids or an acid generating compound which are effective lubricity additives for lube oils, greases, or distillate fuels. [0010]
  • U.S. Pat. No. 5,578,556 relates to triazole-dialkyl maleate derivatives which are described as effective metal passivators and antiwear additives for lubricants and fuels. [0011]
  • U.S. Pat. No. 5,591,237 describes a fuel additive concentrate package comprising a detergent/dispersant, an organic nitrate combustion improver, and a corrosion inhibitor comprising dimer and/or trimer acid to provide enhanced shelf life stability by treating the concentrate with a shelf life stability amount, for example 1,500 and 10,000 ppm, respectively of acid selected from the group consisting of nitric acid/hydrochloric acid. [0012]
  • U.S. Pat. No. 5,669,938 describes a fuel composition which comprises a water-in-oil emulsion comprising a major proportion of a hydrocarbonaceous middle distillate fuel and about 1 to about 40 volume percent water, and an emission reducing amount of at least one fuel-soluble organic nitrate ignition improver such as 2-ethylhexyl nitrate providing reduction of exhaust emissions from diesel engines. [0013]
  • U.S. Pat. No. 5,782,937 relates to fuel compositions containing hydrocarbon fuels in the gasoline boiling range and organic nitrogen-containing compounds selected from organic nitrates and/or organic nitro compounds. The fuel compositions exhibit improved ignition properties, including reduced emissions and reduced misfires. [0014]
  • U.S. Pat. No. 5,944,858 relates to hydrocarbonaceous fuels and additive compositions therefor which comprise: a) one or more fuel-soluble manganese carbonyl compounds; and b) one or more fuel soluble alkali or alkaline earth metal containing neutral or basic detergent salts and preferably, also contain c) one or more of fuel-soluble ashless dispersants; d) at least one fuel soluble demulsifying agent; e) at least one aliphatic or cycloaliphatic amine; and f) at least one metal deactivator. The fuel compositions are said to possess improved combustion characteristics. [0015]
  • U.S. Pat. No. 5,928,392 describes a burner operated by continuously feeding into its combustion zone while combustion is occurring therein, (a) a middle distillate burner fuel with which has been blended a minor combustion improving amount of manganese polycarbonyl compound and a total amount of air above 100% of the stoichiometric amount required for complete combustion of all fuel being introduced into said zone but which is below 105% of such stoichiometric amount. Preferably, alkali or alkaline earth metal containing detergent and fuel soluble dispersant have been blended into the fuel. [0016]
  • European Patent EP 0420581A1 describes an additive for hydrocarbon fuels which includes ethanolamine nitrate as an additive to reduce the quantity of smoke and improve the efficiency of combustion. Fuels are improved by the addition of the additive, which can be prepared by the reaction of ammonium nitrate and anhydrous ethanol in the presence of one or more nitro compounds of formula [0017]
    Figure US20040093790A1-20040520-C00001
  • where R is a hydrogen atom or a C[0018] 1-4 alkyl radical, at a temperature of not more than 40-45° C., the nitro derivative being applied in a concentration of 1 to 3% by weight, the molar ratio between the nitro compound(s) and the ammonium nitrate being at least 0.05:1.
  • Several means are available for reducing emissions, extending hydrocarbon based, especially hydrocarbon, fuels or both. These include, for example, addition of oxygenates to the fuel or incorporating therein significant amounts of water, usually as an emulsion. Since oxygenates typically have reduced fuel value compared to purely hydrocarbon fuels, and, of course, water has no fuel value, the use thereof will often result in a noticeable loss of ‘driveability’, i.e., performance. It is desirable to find additive systems that provide combustion improvement to a wide variety of normally liquid fuels, and particularly to fuels containing oxygenates or water. The instant invention addresses this need. The combustion improvers of this invention are also useful to improve performance of poor driveability fuels. [0019]
  • SUMMARY OF THE INVENTION
  • The instant invention is directed to fuel compositions comprising a major amount of a normally liquid hydrocarbon based fuel and a minor amount of a hydroxylamine or a salt thereof. More often, each hydroxylamino group of the hydroxylamine or salt thereof contains no more than one tertiary alkyl substituent. The hydroxylamine or salt thereof provides improved combustion properties to a wide variety of normally liquid hydrocarbon based fuels, including fuels such as hydrocarbon fuels, biomass fuels and oxygenates. The invention also is directed to a method for improving the combustion characteristics of a normally liquid hydrocarbon based fuel comprising incorporating therein a combustion improving amount of a hydroxylamine or a salt thereof.[0020]
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • As used herein, the terms “hydrocarbyl” or “hydrocarbon based” mean that the group being described has predominantly hydrocarbon character within the context of this invention. These include groups that are purely hydrocarbon in nature, that is, they contain only carbon and hydrogen. They may also include groups containing substituents or atoms which do not alter the predominantly hydrocarbon character of the group. Such substituents may include halo-, alkoxy-, nitro-, hydroxyl, etc. These groups also may contain hetero atoms. Suitable hetero atoms will be apparent to those skilled in the art and include, for example, sulfur, nitrogen and oxygen. Therefore, while remaining predominantly hydrocarbon in character within the context of this invention, these groups may contain atoms other than carbon present in a chain or ring otherwise composed of carbon atoms. [0021]
  • In general, no more than about three non-hydrocarbon substituents or hetero atoms, and preferably no more than one, will be present for every 10 carbon atoms in the hydrocarbon or hydrocarbon based groups. Most preferably, the groups are purely hydrocarbon in nature, that is they are essentially free of atoms other than carbon and hydrogen. [0022]
  • It must be noted that as used in this specification and in the appended claims, the singular forms also include the plural unless the context clearly dictates otherwise. Thus the singular forms “a”, “an”, and “the” include the plural; for example “an amine” includes mixtures of amines of the same type. As another example the singular form “amine” is intended to include both singular and plural unless the context clearly indicates otherwise. [0023]
  • Hydroxylamines and Salts Thereof [0024]
  • The fuel compositions of this invention comprise at least one hydroxylamine or a salt thereof. More often, each hydroxylamino group of the hydroxylamine or salt thereof contains no more than one tertiary alkyl substituent. [0025]
  • In one embodiment, the hydroxylamine has the general formula [0026]
    Figure US20040093790A1-20040520-C00002
  • wherein each of R[0027] a and Rb is, independently, a member selected from the group consisting of H, a primary hydrocarbyl group and a secondary hydrocarbyl group, particularly, H or a hydrocarbyl group containing from 1 to about 25 carbon atoms, and especially a lower alkyl group, and n ranges from 1 to about 30, preferably, from 1 to about 4, and most preferably, 1. Of course, it is obvious that when Ra is H, then n equals 1.
  • Particularly preferred is where each hydrocarbyl group is, independently, a primary alkyl group, especially one containing from 1 to about 6 carbon atoms. [0028]
  • In another embodiment, the hydroxylamine has the general formula [0029]
    Figure US20040093790A1-20040520-C00003
  • wherein each R[0030] c is, independently, H or a hydrocarbyl group, particularly, H or a lower alkyl group, each Rd is, independently, a lower alkylene group, preferably an ethylene or propylene group, most preferably, an ethylene group, and x ranges from 1 to about 29, preferably, from 1 to about 5.
  • Examples of hydroxylamines, which hydroxylamine have been found to be useful as combustion improvers and methods for preparing them are described in numerous Unites States patents including, for example, U.S. Pat. No. 3,491,151; U.S. Pat. No. 4,017,512; U.S. Pat. No. 5,731,462; U.S. Pat. No. 5,733,935 and U.S. Pat. No. 6,031,130. It should be noted that these patents also describe embodiments which are not contemplated as being part of the instant invention and it is not intended that such embodiments are to be considered as being part of the instant invention. These patents are hereby incorporated herein by reference for descriptions of the hydroxylamines that are described herein as useful in this invention. [0031]
  • In another preferred embodiment, the fuel composition comprises a hydroxylamine salt. Hydroxylamines from which the hydroxylamine salts are derived are the same as the hydroxylamines described hereinabove. Typically, the salt is at least one member of the group consisting of nitrates, sulfates, sulfonates, carbonates and carboxylates. Nitrates and carbonates are preferred with nitrates being particularly preferred. The salts are generally obtained by contacting a hydroxylamine with an appropriate acid, optionally, in the presence of a diluent. Many of these salts are commercially available, for example, from chemical supply houses such as Aldrich Chemical Company, Milwaukee, Wis., USA. [0032]
  • The Fuels [0033]
  • The fuels of this invention include all normally liquid hydrocarbon based fuels known in the art. By ‘normally liquid’ is meant a fuel which is liquid or liquefiable at normal operating temperatures. By ‘hydrocarbon based’ means the fuel contains hydrocarbon moieties. These fuels include gasoline meeting ASTM Specification D-4814, diesel fuel meeting ASTM Specification D-975, heating oil meeting ASTM Specification D-396, oxygenates, mixtures of predominantly hydrocarbon fuels and oxygenates, biomass fuel and synthetic fuels. [0034]
  • Hydrocarbon based fuels are those fuels that contain hydrocarbon groups, and especially those that are substantially hydrocarbon, that is, those fuels derived from mineral oil sources, for example, gasoline and middle distillate oils, diesel oil and heating oils, synthetic hydrocarbon fuels such as polyolefins, alkylated aromatic hydrocarbon group containing fuels, hydrocarbon fuels obtained by the Fischer-Tropsch process, and others. [0035]
  • Mixtures of hydrocarbon based fuels and oxygenates include mixtures of any of the aforementioned hydrocarbon based fuels with any of alkanols, especially lower alkanols, and ethers, for example, methyl-t-butyl ether, methyl-t-amyl ether, dimethoxymethane and diethoxymethane, and particularly, lower alkanols such as ethanol. [0036]
  • Biomass fuels are derived from organic materials, such as seeds. Processes for obtaining these oils from biomass are described in numerous U.S. Patents, many of which are listed in U.S. Pat. No. 6,166,231 which is hereby incorporated herein by reference for relevant disclosures of such oils and methods for obtaining them. Examples of biomass fuels are vegetable oil, for example, sunflower oil and rapeseed oils. [0037]
  • The fuel compositions of this invention comprise a minor amount of hydroxylamine or salt thereof. More typically, the fuel compositions comprise from about 50 to about 50,000 parts by weight, even more often from about 1,000 to about 10,000 or to about 5,000 parts by weight, hydroxylamine or salt thereof per million parts by weight of fuel. [0038]
  • The fuel compositions of the present invention may contain other additives which are well known to those skilled in the art. These can include combustion modifiers, such as octane number enhancers for gasoline, for example, anti-knock agents such as tetra-alkyl lead compounds and certain ethers, cetane number improvers for diesel fuels such as alkyl nitrates, lead scavengers such as halo-alkanes, dyes, antioxidants such as hindered phenols, lubricity agents, cold flow improvers, dispersants, surfactants, rust inhibitors such as alkylated succinic acids and anhydrides and derivatives thereof, bacteriostatic agents, auxiliary dispersants and detergents, gum inhibitors, fluidizers, metal deactivators, demulsifiers, anti-icing agents and the like. The fuel compositions of this invention may be lead-containing or lead-free fuels. Preferred are lead-free fuels. [0039]
  • The following examples illustrate several compositions of this invention. All parts are parts by weight. These examples are intended to be for the purpose of illustration only, and are not intended to be limiting of the scope of the claims. Unless indicated otherwise, all amounts of components are given on a neat, diluent-free basis. [0040]
  • EXAMPLE 1
  • A fuel composition is prepared by mixing together, at high speed, 85 parts of a low sulfur No. 2 fuel oil, 15 parts anhydrous ethanol and 0.5 parts N,N-diethylhydroxylamine. [0041]
  • EXAMPLE 2
  • A fuel composition is prepared by mixing together 100 parts of a low sulfur No. 2 fuel oil and 0.5 parts N,N-diethylhydroxylamine. [0042]
  • EXAMPLE 3
  • A fuel composition contains 95 parts unleaded gasoline and 5 parts methanol emulsified with 1.0 part of a 1:1 by weight mixture of a polyether amine prepared by reductive cyanoethylation of C[0043] 12-15 substituted polyoxypropylene monool and a N,N-diethylhydroxylamine hexadecyl substituted succinic ester-salt prepared by reacting one mole each of hexadecyl substituted succinic anhydride with dimethylethanolamine to which emulsion is added 0.5 part N,N-diethylhydroxylamine.
  • EXAMPLE 4
  • A fuel composition contains 96.33 parts diesel fuel, 1.0 parts C[0044] 12-15 alkyl poly(oxypropyl)24 propyl amine, 1 part hexadecenyl succinic dimethylaminoethyl ester-salt and 1.67 parts 13M aqueous hydroxylammonium nitrate.
  • EXAMPLE 5
  • A fuel composition contains 99.50 parts gasoline and 0.5 part N,N-diethylhydroxylamine. [0045]
  • It is known that some of the materials described above may interact in the final formulation, so that the components of the final formulation may be different from those that are initially added. For instance, metal ions (of, e.g., a detergent) can migrate to other acidic sites of other molecules. The products formed thereby, including the products formed upon employing the composition of the present invention in its intended use, may not susceptible of easy description. Nevertheless, all such modifications and reaction products are included within the scope of the present invention; the present invention encompasses the composition prepared by admixing the components described above. [0046]
  • Each of the documents referred to above is incorporated herein by reference. Except in the examples, or where otherwise explicitly indicated, all numerical quantities in this description specifying amounts of materials, reaction conditions, molecular weights, number of carbon atoms, and the like, are to be understood as modified by the word “about”. Unless otherwise indicated, each chemical or composition referred to herein should be interpreted as being a commercial grade material which may contain the isomers, by-products, derivatives, and other such materials which are normally understood to be present in the commercial grade. However, the amount of each chemical component is presented exclusive of any solvent or diluent oil which may be customarily present in the commercial material, unless otherwise indicated. It is to be understood that the upper and lower amount, range, and ratio limits set forth herein may be independently combined. As used herein, the expression “consisting essentially of” permits the inclusion of substances which do not materially affect the basic and novel characteristics of the composition under consideration. [0047]
  • While the invention has been explained in relation to its preferred embodiments, it is to be understood that various modifications thereof will become apparent to those skilled in the art upon reading the specification. Therefore, it is to be understood that the invention disclosed herein is intended to cover such modifications that fall within the scope of the appended claims. [0048]

Claims (46)

What is claimed is:
1. A fuel composition comprising a major amount of a normally liquid hydrocarbon based fuel and a minor amount of a hydroxylamine salt.
2. The fuel composition of claim 1 wherein each hydroxylamino group of the hydroxylamine salt contains no more than one tertiary alkyl substituent.
3. The fuel composition of claim 1 comprising a hydroxylamine salt wherein the hydroxylamine has the general formula
Figure US20040093790A1-20040520-C00004
wherein each of Ra and Rb is, independently, a member selected from the group consisting of H, a primary hydrocarbyl group and a secondary hydrocarbyl group, and n ranges from 1 to about 30.
4. The fuel composition of claim 3 wherein n ranges from 1 to about 4.
5. The fuel composition of claim 4 wherein n=1 and each of Ra and Rb is, independently, H or a hydrocarbyl group, containing from 1 to about 25 carbon atoms.
6. The fuel composition of claim 5 wherein each of Ra and Rb is, independently, a lower alkyl group.
7. The fuel composition of claim 4 wherein each hydrocarbyl group is, independently, a primary alkyl group.
8. The fuel composition of claim 7 wherein each primary alkyl group, independently contains from 1 to about 6 carbon atoms.
9. The fuel composition of claim 1 comprising a hydroxylamine salt wherein the hydroxylamine has the general formula
Figure US20040093790A1-20040520-C00005
wherein each Rc is, independently, H or a hydrocarbyl group, each Rd is, independently, a lower alkylene group and x ranges from 1 to about 29.
10. The fuel composition of claim 9 wherein each Rc is, independently, H or a lower alkyl group and each Rd is independently an ethylene or propylene group.
11. The fuel composition of claim 1 wherein the salt is at least one member of the group consisting of nitrates, sulfates, sulfonates, carbonates and carboxylates.
12. The fuel composition of claim 11 wherein the salt is selected from the group consisting of nitrates and carbonates.
13. The fuel composition of claim 12 wherein the salt is a nitrate.
14. The fuel composition of claim 1 wherein the fuel comprises gasoline meeting ASTM Specification D-4814.
15. The fuel composition of claim 1 wherein the fuel comprises diesel fuel meeting ASTM Specification D-975.
16. The fuel composition of claim 1 wherein the fuel comprises heating oil meeting ASTM Specification D-396.
17. The fuel composition of claim 1 wherein the fuel comprises oxygenates.
18. The fuel composition of claim 17 wherein the oxygenates comprise at least one member of the group consisting of lower alkanols and ethers.
19. The fuel composition of claim 1 wherein the fuel comprises a mixture of a hydrocarbon fuel and a lower alkanol.
20. The fuel composition of claim 19 wherein the hydrocarbon fuel is gasoline.
21. The fuel composition of claim 19 wherein the hydrocarbon fuel is diesel fuel.
22. The fuel composition of claim 1 wherein the fuel comprises a biomass fuel.
23. The fuel composition of claim 22 wherein the biomass fuel comprises vegetable oil.
24. The fuel composition of claim 1 wherein the fuel is a synthetic fuel.
25. The fuel composition of claim 24 wherein the synthetic fuel is obtained by the Fischer-Tropsch process
26. The fuel composition of claim 25 wherein the synthetic fuel is a hydrocarbon fuel.
27. A method for improving the combustion characteristics of a normally liquid hydrocarbon based fuel comprising incorporating therein a combustion improving amount of a hydroxylamine salt.
28. The method of claim 27 wherein each hydroxylamino group of the hydroxylamine salt contains no more than one tertiary alkyl substituent.
29. The fuel composition of claim 1 wherein the hydroxylamine or salt thereof is present in amounts ranging from about 50 to about 50,000 parts by weight per million parts by weight of fuel.
30. A fuel composition comprising a major amount of gasoline meeting ASTM Specification D-4814 and a minor amount of a hydroxylamine or a salt thereof wherein each hydroxylamino group of the hydroxylamine or salt thereof contains no more than one tertiary alkyl substituent.
31. The fuel composition of claim 30 comprising a hydroxylamine wherein the hydroxylamine has the general formula
Figure US20040093790A1-20040520-C00006
wherein each of Ra and Rb is, independently, a member selected from the group consisting of H, a primary hydrocarbyl group and a secondary hydrocarbyl group, and n ranges from 1 to about 30.
32. The fuel composition of claim 31 wherein n ranges from 1 to about 4.
33. The fuel composition of claim 32 wherein n=1 and each of Ra and Rb is, independently, H or a hydrocarbyl group, containing from 1 to about 25 carbon atoms.
34. The fuel composition of claim 33 wherein each of Ra and Rb is, independently, a lower alkyl group.
35. The fuel composition of claim 32 wherein each hydrocarbyl group is, independently, a primary alkyl group.
36. The fuel composition of claim 356 wherein each primary alkyl group, independently contains from 1 to about 6 carbon atoms.
37. The fuel composition of claim 30 comprising a hydroxylamine wherein the hydroxylamine has the general formula
Figure US20040093790A1-20040520-C00007
wherein each Rc is, independently, H or a hydrocarbyl group, each Rd is, independently, a lower alkylene group and x ranges from 1 to about 29.
38. The fuel composition of claim 37 wherein each Rc is, independently, H or a lower alkyl group and each Rd is independently an ethylene or propylene group.
39. The fuel composition of claim 30 wherein the fuel comprises a mixture of gasoline and a lower alkanol.
40. The fuel composition of claim 30 wherein the gasoline is a synthetic fuel.
41. The fuel composition of claim 40 wherein the gasoline is obtained by the Fischer-Tropsch process
42. A method for improving the combustion characteristics of a gasoline fuel comprising incorporating therein a combustion improving amount of a hydroxylamine or a salt thereof wherein each hydroxylamino group of the hydroxylamine or salt thereof contains no more than one tertiary alkyl substituent.
43. The fuel composition of claim 30 wherein the hydroxylamine or salt thereof is present in amounts ranging from about 50 to about 50,000 parts by weight per million parts by weight of fuel.
44. The fuel composition of any one of claims 1-26, 29-41 and 43, further comprising at least one component selected from the group consisting of a) dispersants, b) combustion modifiers, c) lubricity agents, d) cold flow improvers, e) fluidizers and (f) surfactants.
45. The method of any one of claims 27, 28 and 42 wherein the improved combustion characteristics comprise at least one of reduced particulate emissions, reduced NOx emissions, improved fuel efficiency and reduced hydrocarbon emissions.
46. A method for operating an internal combustion engine or a burner comprising providing to the combustion chamber of said engine or burner during operation thereof, the fuel composition of any one of claims 1 and 30.
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