US3416901A - Motor fuels containing ether acids - Google Patents

Motor fuels containing ether acids Download PDF

Info

Publication number
US3416901A
US3416901A US699942A US69994257A US3416901A US 3416901 A US3416901 A US 3416901A US 699942 A US699942 A US 699942A US 69994257 A US69994257 A US 69994257A US 3416901 A US3416901 A US 3416901A
Authority
US
United States
Prior art keywords
octane
ether
acid
lead
fuel
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US699942A
Inventor
George W Eckert
Howard V Hess
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Texaco Inc
Original Assignee
Texaco Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US689466A external-priority patent/US3541723A/en
Application filed by Texaco Inc filed Critical Texaco Inc
Priority to US699942A priority Critical patent/US3416901A/en
Priority to DK365958A priority patent/DK106708C/en
Priority to CH6490958A priority patent/CH376714A/en
Application granted granted Critical
Publication of US3416901A publication Critical patent/US3416901A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

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
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic 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
    • C10L1/185Ethers; Acetals; Ketals; Aldehydes; Ketones
    • C10L1/1857Aldehydes; Ketones
    • 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
    • C10L1/1881Carboxylic acids; metal salts thereof carboxylic group attached to an aliphatic carbon atom
    • 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
    • C10L1/189Carboxylic acids; metal salts thereof having at least one carboxyl group bound to an aromatic carbon atom
    • 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
    • C10L1/19Esters ester radical containing compounds; ester ethers; carbonic acid esters
    • 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
    • C10L1/30Organic compounds compounds not mentioned before (complexes)
    • C10L1/305Organic compounds compounds not mentioned before (complexes) organo-metallic compounds (containing a metal to carbon bond)
    • C10L1/306Organic compounds compounds not mentioned before (complexes) organo-metallic compounds (containing a metal to carbon bond) organo Pb compounds

Definitions

  • This invention relates to a hydrocarbon fuel composition of high octane rating. More specifically, it involves the discovery that the octane rating of leaded gasoline fuels is substantially improved by the addition of ether carboxylic acids.
  • Catalytic cracking and catalytic reforming which are the most widely used refining operations in the production of high octane fuels, produce substantial quantities of aromatics; catalytic cracking also produces a substantial amount of olefins. It is well known that olefins and aromatics, although possessing high octane ratings, have a poorer response to organo-lead compounds such as tetraethyl lead than saturated aliphatic gasoline components. Accordingly, as the aromatic and olefinic contents of the gasolines have increased to meet the octane levels required by modern automotive high compression engines, the lead response of the resulting fuels has diminished.
  • the octane increment obtainable by the addition of an organo-lead compound decreases as the aromatic and olefin contents of the base fuel increase.
  • the subject invention involves the discovery that the octane rating of leaded motor fuels containing a substantial concentration of high octane components, that is, aromatics, olefins and mixtures thereof, is markedly improved by the addition of a small amount of an ether monocarboxylic acid.
  • the high octane hydrocarbon motor fuel of this invention comprises high octane components including a substantial concentration of aromatic hydrocarbons, olefinic hydrocarbons or mixtures thereof, an organo-lead antiknock agent and an ether monocarboxylic acid in a concentration of at least 0.1 volume percent of fuel.
  • ether monocarboxylic acids in raising the octane rating of gasoline is characterized by several unusual features.
  • ether carboxylic acids appear to be ineffective in raising the octane rating 3,416,901 Patented Dec. 17, 1968 of gasolines unless an organo-lead anti-knock agent, normally tetraethyl lead, is a component of the gasoline mixture.
  • the second unusual characteristic of the action of ether monocarboxylic acids in appreciating the octane rating of gasolines is the fact that an equivalent concentration of acids appears to cause a greater octane improvement above the 100 octane level than below the 100 octane level.
  • ether monocarboxylic acids have their minimum effects where tetraethyl lead has its maximum effeet and exert their maximum effect on octane values where tetraethyl lead has its minimum effect.
  • novel fuel compositions of this invention have a minimum concentration of aromatic and/or olefin components of at least 10 volume percent.
  • the aromatic and/ or olefin components of the motor fuel of the invention can constitute as high as 100 volume percent thereof but usually comprise between 20 and volume percent.
  • the minimum 10 percent concentration is necessary for ether monocarboxylic acids to exert a significant octane improvement.
  • the aromatic components of the motor fuel of the invention are generally supplied by catalytic reforming or catalytic cracking operations. Catalytic reformate is particularly high in aromatics.
  • the olefin components of the motor fuel of the invention are derived either from thermal cracking, catalytic cracking or. polymerization.
  • the organo-lead reagent necessary for the action of ether monocarboxylic acids as octane improvers is a tetraalkyl lead compound of the class known to possess anti-knock action.
  • Tetraethyl lead is practically universally used as an -anti-knock agent but other tetraalkyl lead compounds such as tetramethyl lead, tetrabutyl lead, tetraamyl lead, tetrapropyl lead, etc. are known to possess anti-knock properties and may be usedin the fuel compositions of the invention in conjunctionwith ether monocarboxylic acids.
  • tetraethyl lead mixtures commercially available for automotive use contain an ethylene chloride-ethylene bromide mixture as a scavenger for removing lead from the combustion chamber in the form of volatile lead halides.
  • tetraethyl lead fluid denotes the commercial product which comprises tetraethyl lead, ethylene chloride and ethylene bromide, the latter two reagents being present in 1.0 theory and 0.5 theory, respectively, theory denoting the stoichiometric amount required for reaction with the lead content of the tetraethyl lead.
  • the organo-lead reagent is present in the fuel compositions of the invention in concentrations between 0.5 ml. per gallon up to the statutory limit of organo-lead reagent concentration which, at the present time, is 3 ml. per gallon in the case of automotive fuel and 4.6 ml. per gallon in the case of aviation fuel.
  • the usual concentration of tetraethyl lead is between 1 and 3 ml. per gallon in automotive gasoline and 2 to 4.6 ml. per gallon in aviation gasoline.
  • Ether acids which are effective in increasing the octane rating of an aromatic and/or olefin-containing gasoline in the presence of an organo-lead anti-knock agent contain 330 carbon atoms and have the general formula: ROR'COOH wherein R is a monovalent hydrocarbyl radical containing 1-l8 and preferably 1-12 carbon atoms and R is a divalent hydrocarbyl radical containing 1-12 carbon atoms and preferably l-8 carbon atoms. Although both R and R can be aliphatic, cycloaliphatic or aromatic hydrocarbyl radicals, R is generally a divalent aliphatic hydrocarbyl radical and R is generally an aryl hydrocarbyl radical or an aliphatic hydrocarbyl radical.
  • Preferred ether acids are alkoxy aliphatic monocarboxylic acids and aryloxy aliphatic monocarboxylic acids.
  • ether acids effective as octane improvers in the fuel compositions of the invention are methoxyacetic acid, ethoxyacetic acid, phenoxyacetic acid, tolyloxyacetic acid, 3-ethoxypropionic acid, Z-methoxypropionic acid, 2- ethoxy n-octanoic acid, 2-phenoxy n-hexanoic acid, 2- methoxy n-dodecanoic acid, 3-isopropoxy 2-ethylhexanoic acid, and ortho-ethoxybenzoic acid.
  • ether-substituted monocarboxylic acids in raising the octane rating of leaded fuels containing an aromatic and/or olefin content is particularly surprising in view of the fact that other substituted monocarboxylic acids such as hydroxy monocarboxylic acids, halogenated monocarboxylic acids and sulfhydryl-substituted monocarboxylic acids are ineffective as anti-knock agents in the fuel compositions of the invention.
  • the ether monocarboxylic acids must be present in the leaded aromatic and/or olefin-containing compositions of the invention in a minimum concentration of 0.1 volume percent before a significant octane appreciation is realized.
  • the preferred concentration of ether monocarboxylic acid in the fuel compositions of the invention falls between 0.2 and 1.0 volume percent with maximum octane appreciation generally being obtained at a concentration level of about 0.5 volume percent. Concentrations of ether monocarboxylic acids as high as volume percent can be incorporated in the fuel compositions but no additional octane improvement is realized at the higher concentrations and economic considerations preclude the use of such concentrations in commercial fuel compositions.
  • the base fuel to which the ether acids were added in the concentration of about 0.5 volume percent was a catalytically reformed naphtha containing 3 cc. of tetraethyl lead fluid per gallon and having an IBP of 130 F. and an end point of 394 F.
  • the base fuel had a leaded Research Octane Rating of 96.6 and an aromatic concentration of 48 volume percent as measured by Fluorescent Indicator Analysis (PIA) Method.
  • Base fuel 96.6 Base fuel+0.5 v. percent methoxyacetic acid 98.0
  • the data in the table also indicate the specificity of ether acids in raising the octane rating of leaded fuels containing an aromatic and/ or olefin content. While the ether acids effected better than a 1 unit improvement in research octane rating, the halogenated acids, hydroxy acids and mercapto acids either had no effect or substantially decreased the research octane rating of the leaded catalytic reformate.
  • a hydrocarbon fuel in the gasoline boiling range containing a tetraalkyl lead antiknock agent, substantial quantities of high octane components selected from the group consisting of olefinic hydrocarbons, aromatic hydrocarbons and mixtures thereof and an ether hydrocarbyl monocarbox-ylic acid in an amount sufiicient to improve the octane rating of said hydrocarbon fuel.
  • a hydrocarbon fuel in the gasoline boiling range containing an organo-lead anti-knock agent, high octane components selected from the group consisting of olefinic hydrocarbons, aromatic hydrocarbons, and mixtures thereof in a concentration of at least 10 volume percent, and an ether hydrocarbyl monocarboxylic acid containing 3 to 30 carbon atoms, said ether acid being present in a concentration between 0.1 and 5.0 volume percent, said concentration being sufficient to effect substantial improvement of the octane rating of said hydrocarbon fuel.
  • a hydrocarbon fuel in the gasoline boiling range containing a tetraalkyl lead anti-knock agent in a concentration of at least 0.5 cc. per gallon, high octane components selected from the group consisting of olefinic hydrocarbons, aromatic hydrocarbons and mixtures thereof in a concentration of at least 10 volume percent of said fuel and an ether acid of the general formula ROR'COOH in which R is a monovalent hydrocarbyl radical containing l-l2 carbon atoms and R is a divalent hydrocarbyl radical containing l-8 carbon atoms in a concentration of 0.1 to 5.0 volume percent.
  • a hydrocarbon fuel according to claim 5 containing 1.0 to 4.6 cc. of tetraethyl lead per gallon.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Liquid Carbonaceous Fuels (AREA)

Description

United States Patent 3,416,901 MOTOR FUELS CONTAINING ETHER ACIDS George W. Eckert, Wappingers Falls, and Howard V.
Hess, Glenham, N.Y., assignors to Texaco Inc., a corporation of Delaware N0 Drawing. Filed Dec. 2, 1957, Ser. No. 699,942 10 Claims. (Cl. 4469) This invention relates to a hydrocarbon fuel composition of high octane rating. More specifically, it involves the discovery that the octane rating of leaded gasoline fuels is substantially improved by the addition of ether carboxylic acids.
The recent increases in compression ratios of automobile engines have placed a severe strain on petroleum refiners to produce fuels having the octane rating demanded by these engines. Premium fuels at the present time have research octane ratings between 97 and 100 and it has been predicted that premium fuels will have to have octane ratings between 105 and 110 five years from now in order to satisfy the octane requirements of the high compression automotive engines predicted for that date. In order to produce premium fuels of octane ratings of 95 and above, it has been necessary for refiners to rely heavily on catalytic refining operations such as fluid catalytic cracking, catalytic reforming, alkylation and catalytic isomerization.
Catalytic cracking and catalytic reforming, which are the most widely used refining operations in the production of high octane fuels, produce substantial quantities of aromatics; catalytic cracking also produces a substantial amount of olefins. It is well known that olefins and aromatics, although possessing high octane ratings, have a poorer response to organo-lead compounds such as tetraethyl lead than saturated aliphatic gasoline components. Accordingly, as the aromatic and olefinic contents of the gasolines have increased to meet the octane levels required by modern automotive high compression engines, the lead response of the resulting fuels has diminished. Stated another way, the octane increment obtainable by the addition of an organo-lead compound decreases as the aromatic and olefin contents of the base fuel increase. The subject invention involves the discovery that the octane rating of leaded motor fuels containing a substantial concentration of high octane components, that is, aromatics, olefins and mixtures thereof, is markedly improved by the addition of a small amount of an ether monocarboxylic acid.
In the copending application Ser. No. 689,466, filed Oct. 11, 1957, it is disclosed that monocarboxylic acids in prescribed concentration substantially raise the octane rating of -a motor fuel containing an organo-lead antiknock agent and a substantial concentration of high octane components which may be aromatic hydrocarbons, olefinic hydrocarbons or mixtures thereof. The subject invention involves the discovery that ether monocarboxylic acids exert a similar anti-knock action in motor fuel compositions of the prescribed type.
The high octane hydrocarbon motor fuel of this invention comprises high octane components including a substantial concentration of aromatic hydrocarbons, olefinic hydrocarbons or mixtures thereof, an organo-lead antiknock agent and an ether monocarboxylic acid in a concentration of at least 0.1 volume percent of fuel.
The action of ether monocarboxylic acids in raising the octane rating of gasoline is characterized by several unusual features. In the first instance, ether carboxylic acids appear to be ineffective in raising the octane rating 3,416,901 Patented Dec. 17, 1968 of gasolines unless an organo-lead anti-knock agent, normally tetraethyl lead, is a component of the gasoline mixture.
The second unusual characteristic of the action of ether monocarboxylic acids in appreciating the octane rating of gasolines is the fact that an equivalent concentration of acids appears to cause a greater octane improvement above the 100 octane level than below the 100 octane level.
The third unusual feature of the action of ether monocarboxylic acids is that they appear to have substantially no effect on the octane rating of a gasoline consisting essentially of saturated aliphatic hydrocarbons even though an organo-lead anti-knock agent is present. Since organolead anti-knock agents exert their greatest octane appreciation in predominantly saturated paraflinic base hydrocarbon gasolines and have the least effect on the octane rating of aromatic and olefin rich gasolines, the present invention neatly complements tetraethyl lead as an octane improver. Ether monocarboxylic acids have their minimum effects where tetraethyl lead has its maximum effeet and exert their maximum effect on octane values where tetraethyl lead has its minimum effect.
The novel fuel compositions of this invention have a minimum concentration of aromatic and/or olefin components of at least 10 volume percent. The aromatic and/ or olefin components of the motor fuel of the invention can constitute as high as 100 volume percent thereof but usually comprise between 20 and volume percent. The minimum 10 percent concentration is necessary for ether monocarboxylic acids to exert a significant octane improvement.
The aromatic components of the motor fuel of the invention are generally supplied by catalytic reforming or catalytic cracking operations. Catalytic reformate is particularly high in aromatics. The olefin components of the motor fuel of the invention are derived either from thermal cracking, catalytic cracking or. polymerization.
The organo-lead reagent necessary for the action of ether monocarboxylic acids as octane improvers is a tetraalkyl lead compound of the class known to possess anti-knock action. Tetraethyl lead is practically universally used as an -anti-knock agent but other tetraalkyl lead compounds such as tetramethyl lead, tetrabutyl lead, tetraamyl lead, tetrapropyl lead, etc. are known to possess anti-knock properties and may be usedin the fuel compositions of the invention in conjunctionwith ether monocarboxylic acids.
The tetraethyl lead mixtures commercially available for automotive use contain an ethylene chloride-ethylene bromide mixture as a scavenger for removing lead from the combustion chamber in the form of volatile lead halides. As used hereafter in the examples illustrating the invention, tetraethyl lead fluid denotes the commercial product which comprises tetraethyl lead, ethylene chloride and ethylene bromide, the latter two reagents being present in 1.0 theory and 0.5 theory, respectively, theory denoting the stoichiometric amount required for reaction with the lead content of the tetraethyl lead.
The organo-lead reagent is present in the fuel compositions of the invention in concentrations between 0.5 ml. per gallon up to the statutory limit of organo-lead reagent concentration which, at the present time, is 3 ml. per gallon in the case of automotive fuel and 4.6 ml. per gallon in the case of aviation fuel. The usual concentration of tetraethyl lead is between 1 and 3 ml. per gallon in automotive gasoline and 2 to 4.6 ml. per gallon in aviation gasoline.
Ether acids which are effective in increasing the octane rating of an aromatic and/or olefin-containing gasoline in the presence of an organo-lead anti-knock agent contain 330 carbon atoms and have the general formula: ROR'COOH wherein R is a monovalent hydrocarbyl radical containing 1-l8 and preferably 1-12 carbon atoms and R is a divalent hydrocarbyl radical containing 1-12 carbon atoms and preferably l-8 carbon atoms. Although both R and R can be aliphatic, cycloaliphatic or aromatic hydrocarbyl radicals, R is generally a divalent aliphatic hydrocarbyl radical and R is generally an aryl hydrocarbyl radical or an aliphatic hydrocarbyl radical. Preferred ether acids are alkoxy aliphatic monocarboxylic acids and aryloxy aliphatic monocarboxylic acids.
Examples of ether acids effective as octane improvers in the fuel compositions of the invention are methoxyacetic acid, ethoxyacetic acid, phenoxyacetic acid, tolyloxyacetic acid, 3-ethoxypropionic acid, Z-methoxypropionic acid, 2- ethoxy n-octanoic acid, 2-phenoxy n-hexanoic acid, 2- methoxy n-dodecanoic acid, 3-isopropoxy 2-ethylhexanoic acid, and ortho-ethoxybenzoic acid.
The effectiveness of ether-substituted monocarboxylic acids in raising the octane rating of leaded fuels containing an aromatic and/or olefin content is particularly surprising in view of the fact that other substituted monocarboxylic acids such as hydroxy monocarboxylic acids, halogenated monocarboxylic acids and sulfhydryl-substituted monocarboxylic acids are ineffective as anti-knock agents in the fuel compositions of the invention.
The ether monocarboxylic acids must be present in the leaded aromatic and/or olefin-containing compositions of the invention in a minimum concentration of 0.1 volume percent before a significant octane appreciation is realized. When the ether acid concentration is below 0.1 volume percent, no octane improvement is obtained in leaded gasoline containing at least 10 volume percent aromatics and/or olefins. The preferred concentration of ether monocarboxylic acid in the fuel compositions of the invention falls between 0.2 and 1.0 volume percent with maximum octane appreciation generally being obtained at a concentration level of about 0.5 volume percent. Concentrations of ether monocarboxylic acids as high as volume percent can be incorporated in the fuel compositions but no additional octane improvement is realized at the higher concentrations and economic considerations preclude the use of such concentrations in commercial fuel compositions.
In the following table there is shown the action of ether-substituted monocarboxylic acids in raising the octane rating of the leaded fuel compositions of the invention. The base fuel to which the ether acids were added in the concentration of about 0.5 volume percent was a catalytically reformed naphtha containing 3 cc. of tetraethyl lead fluid per gallon and having an IBP of 130 F. and an end point of 394 F. The base fuel had a leaded Research Octane Rating of 96.6 and an aromatic concentration of 48 volume percent as measured by Fluorescent Indicator Analysis (PIA) Method.
TABLE I Research Octane No.
Base fuel 96.6 Base fuel+0.5 v. percent methoxyacetic acid 98.0 Base fuel-+0.5 v. percent ethoxyacetic acid 98.1
Base fuel+0.5 v. percent mono-chloroacetic acid 87.0 Base fuel-{-05 v. percent heptafluoroacetic acid 89.3
Base fuel+0.5 v. percent 2-bromohexanoic acid 96.3 Base fuel-{-05 v. percent mercaptoacetic acid 96.0 Base fuel+0.5 v. percent ricinoleic acid 96.6 Base fuel+0.5 v. percent salicylic acid 96.6
The foregoing data demonstrate very clearly the effectiveness of the prescribed concentration of ether acids in raising the octane rating of a leaded gasoline having the prescribed aromatic content. The improvement in octane rating obtained by the addition of 0.5 volume percent methoxyacetic acid and ethoxyacetic acid is significant.
The data in the table also indicate the specificity of ether acids in raising the octane rating of leaded fuels containing an aromatic and/ or olefin content. While the ether acids effected better than a 1 unit improvement in research octane rating, the halogenated acids, hydroxy acids and mercapto acids either had no effect or substantially decreased the research octane rating of the leaded catalytic reformate.
Obviously, many modifications and variations of the invention as hereinbefore set forth may be made without departing from the spirit and scope thereof and, therefore, only such limitations should be imposed as are indicated in the appended claims.
We claim:
1. A hydrocarbon fuel in the gasoline boiling range containing a tetraalkyl lead antiknock agent, substantial quantities of high octane components selected from the group consisting of olefinic hydrocarbons, aromatic hydrocarbons and mixtures thereof and an ether hydrocarbyl monocarbox-ylic acid in an amount sufiicient to improve the octane rating of said hydrocarbon fuel.
2. A hydrocarbon fuel in the gasoline boiling range containing an organo-lead anti-knock agent, high octane components selected from the group consisting of olefinic hydrocarbons, aromatic hydrocarbons, and mixtures thereof in a concentration of at least 10 volume percent, and an ether hydrocarbyl monocarboxylic acid containing 3 to 30 carbon atoms, said ether acid being present in a concentration between 0.1 and 5.0 volume percent, said concentration being sufficient to effect substantial improvement of the octane rating of said hydrocarbon fuel.
3. A hydrocarbon fuel according to claim 2 in which said ether acid has the general formula: ROR'COOH in which R is a hydrocarbyl radical containing l-18 carbon atoms and R is a divalent hydrocarbyl radical containing 1-12 carbon atoms.
4. A hydrocarbon fuel according to claim 2 in which said organo-lead anti-knock agent is present in a concentration between 0.5 and 4.6 cc. per gallon.
5. A hydrocarbon fuel in the gasoline boiling range containing a tetraalkyl lead anti-knock agent in a concentration of at least 0.5 cc. per gallon, high octane components selected from the group consisting of olefinic hydrocarbons, aromatic hydrocarbons and mixtures thereof in a concentration of at least 10 volume percent of said fuel and an ether acid of the general formula ROR'COOH in which R is a monovalent hydrocarbyl radical containing l-l2 carbon atoms and R is a divalent hydrocarbyl radical containing l-8 carbon atoms in a concentration of 0.1 to 5.0 volume percent.
6. A hydrocarbon fuel according to claim 5 in which the concentration of said ether acid is between 0.2 and 1.0 volume percent.
7. A hydrocarbon fuel according to claim 5 in which said high octane components constitute 20-80 volume percent of said fuel. 0
8. A hydrocarbon fuel according to claim 5 containing 1.0 to 4.6 cc. of tetraethyl lead per gallon.
9. A hydrocarbon fuel according to claim 5 in which said ether acid is methoxy acetic acid.
10. A hydrocarbon fuel according to claim 5 in which said ether acid is ethoxy acetic acid.
References Cited UNITED STATES PATENTS 1,692,784 11/1928 Orelup 6:31 44 66 2,210,942 8/1940 Lipkin 44-77 2,333,726 11/1943 Von Leibitz-Piwnicki- 260-535 2,667,408 1/1954 Kleinholz 4466X (Other references on following page) 5 6 FOREIGN PATENTS Improved Motor Fuels Through Selective Blending, 640 311 3/1928 France Wagner et al., paper presented before American Petro- France' ICUIII Institute, NOV. 7,
837,965 11/1938 France. 1,103,895 6/1955 France- DANIEL E. WYMAN, Primary Examzner.
277,326 1/1929 Great Britain, Y. H. SMITH, Assistant Examiner. 599,222 3/1948 Great Britain. Us CL OTHER REFERENCES

Claims (1)

1. A HYDROCARBON FUEL IN THE GASOLINE BOILING RANGE CONTAINING A TETRAALKYL LED ANTIKNOCK AGENT, SUBSTANTIAL QUANTITIES OF HIGH OCTANE COMPONENTS SELECTED FROM THE GROUP CONSISTING OF OLEFINIC HYDROCARBONS, AROMATIC HYDROCARBONS AND MIXTURES THEREOF AND AN ETHER HYDROCARBYL MONOCARBOXYLIC ACID IN AN AMOUNT SUFFICIENT TO IMPROVE THE OCTANE RATING OF SAID HYDROCARBON FUEL.
US699942A 1957-10-11 1957-12-02 Motor fuels containing ether acids Expired - Lifetime US3416901A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
US699942A US3416901A (en) 1957-10-11 1957-12-02 Motor fuels containing ether acids
DK365958A DK106708C (en) 1957-10-11 1958-10-10 Petrol fuel containing an organoblyane anti-bank agent and at least 10% by volume of high octane constituents consisting of olefinic hydrocarbons, aromatic hydrocarbons or mixtures thereof.
CH6490958A CH376714A (en) 1957-10-11 1958-10-10 Hydrocarbon-based fuels

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US689466A US3541723A (en) 1957-10-11 1957-10-11 Motor fuels containing monocarboxylic acids
US699942A US3416901A (en) 1957-10-11 1957-12-02 Motor fuels containing ether acids

Publications (1)

Publication Number Publication Date
US3416901A true US3416901A (en) 1968-12-17

Family

ID=27104424

Family Applications (1)

Application Number Title Priority Date Filing Date
US699942A Expired - Lifetime US3416901A (en) 1957-10-11 1957-12-02 Motor fuels containing ether acids

Country Status (1)

Country Link
US (1) US3416901A (en)

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR640311A (en) * 1926-09-07 1928-07-10 Avenarius Soc Geb Method and means for preventing knocking caused by motor fuels
US1692784A (en) * 1925-01-23 1928-11-20 Boyce Ite Products Inc Fuel and fuel ingredients
GB277326A (en) * 1927-09-06 1929-01-07 Avenarius Geb A method for preventing the knocking of motor fuel
FR793967A (en) * 1934-11-15 1936-02-05 Savons Nouveaux Cie Sapoflor Anti-knock compounds
FR837965A (en) * 1937-11-08 1939-02-23 Melle Usines Sa Detonation resistant fuels
US2210942A (en) * 1936-10-20 1940-08-13 Atlantic Refining Co Motor fuel
US2333726A (en) * 1938-06-04 1943-11-09 Leibitz-Piwnicki Heinz Von Process of preparing ether acids
GB599222A (en) * 1945-09-21 1948-03-08 Anglo Iranian Oil Co Ltd Improvements relating to motor fuels
US2667408A (en) * 1949-10-05 1954-01-26 Sinclair Refining Co Prevention of rust
FR1103895A (en) * 1953-07-10 1955-11-08 Process for increasing the efficiency of fuels in combustion engines

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1692784A (en) * 1925-01-23 1928-11-20 Boyce Ite Products Inc Fuel and fuel ingredients
FR640311A (en) * 1926-09-07 1928-07-10 Avenarius Soc Geb Method and means for preventing knocking caused by motor fuels
GB277326A (en) * 1927-09-06 1929-01-07 Avenarius Geb A method for preventing the knocking of motor fuel
FR793967A (en) * 1934-11-15 1936-02-05 Savons Nouveaux Cie Sapoflor Anti-knock compounds
US2210942A (en) * 1936-10-20 1940-08-13 Atlantic Refining Co Motor fuel
FR837965A (en) * 1937-11-08 1939-02-23 Melle Usines Sa Detonation resistant fuels
US2333726A (en) * 1938-06-04 1943-11-09 Leibitz-Piwnicki Heinz Von Process of preparing ether acids
GB599222A (en) * 1945-09-21 1948-03-08 Anglo Iranian Oil Co Ltd Improvements relating to motor fuels
US2667408A (en) * 1949-10-05 1954-01-26 Sinclair Refining Co Prevention of rust
FR1103895A (en) * 1953-07-10 1955-11-08 Process for increasing the efficiency of fuels in combustion engines

Similar Documents

Publication Publication Date Title
US3541723A (en) Motor fuels containing monocarboxylic acids
US2310710A (en) Inhibitor for gasoline
US3082070A (en) Motor fuel containing synergistic octane appreciator
US2912313A (en) Diesel fuel
US3009793A (en) Motor fuel containing synergistic anti-knock additive
US3036904A (en) Motor fuel containing octane appreciator
US2860958A (en) Antiknock compositions
US3421867A (en) Saturated aliphatic hydrocarbon gasoline
US3015547A (en) Motor fuel containing octane improver
US3419367A (en) Motor fuel containing octane improver
US3976437A (en) Composition comprising a methyl phenol and an ether for gasoline fuels
US3416901A (en) Motor fuels containing ether acids
US3074787A (en) Motor fuels containing keto carboxylic acids
US3009792A (en) Motor fuel containing synergistic anti-knock additive
US3181938A (en) Motor fuel containing octane appreciator
US3168385A (en) Motor fuels
US3212867A (en) Motor fuel compositions
US3087801A (en) Motor fuel containing octane appreciator
US2275175A (en) Motor fuel
USRE23239E (en) Inhibitor for gasoline
US3021205A (en) Motor fuel
US3377149A (en) Motor fuel containing an octane appreciator
US3085002A (en) Motor fuel compositions
US3359087A (en) Motor fuel containing an octane appreciator
US3087802A (en) Motor fuel containing octane appreciator