US3055746A - Adducts of aliphatic monocarboxylic acids and aliphatic amines in gasoline - Google Patents

Adducts of aliphatic monocarboxylic acids and aliphatic amines in gasoline Download PDF

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US3055746A
US3055746A US811535A US81153559A US3055746A US 3055746 A US3055746 A US 3055746A US 811535 A US811535 A US 811535A US 81153559 A US81153559 A US 81153559A US 3055746 A US3055746 A US 3055746A
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gasoline
adducts
stalling
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George W Eckert
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    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS 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
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/22—Organic compounds containing nitrogen
    • C10L1/222—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS 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
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/22—Organic compounds containing nitrogen
    • C10L1/222—Organic 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
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS 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
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/22—Organic compounds containing nitrogen
    • C10L1/222—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
    • C10L1/224—Amides; Imides carboxylic acid amides, imides

Definitions

  • This invention relates to a volatile gasoline composition of improved anti-stalling properties containing an adduct of a monocarboXylic acid and a high base strength amine of prescribed composition. More particularly, it involves the discovery that adducts of monocarboxylic acids and high base strength amines are effective antistalling additives for gasoline.
  • adducts of a high base strength amine and a C to C hydrocarbyl monocarboxylic acid in a concentration between about 0.2 and 5.0 weight percent act as octane appreciators for leaded gasoline having a prescribed aromatic and/or olefin content.
  • the subject invention involves the discovery that adducts of hydrocarbyl monocarboxylic acids and high base strength amines of prescribed chain length are effective anti-stalling and anti-icing additives for volatile gasolines in substantially lower concentrations than are required for their actions as octane appreciators.
  • the gasoline fuel composition of this invention comprises a substan ial concentration of volatile components, and 0.001 to 0.1 weight percent of an adduct of a C to C alkyl amine having a pka between 8 and 11.5 and a hydrocarbyl monocarboxylic acid containing 2 to 18 carbon atoms, said adduct containing a total of 8 to 20 carbon atoms.
  • the presence of amine-acid adducts of prescribed composition and in prescribed concentration imparts outstanding anti-icing and anti-stalling properties to the resulting gasoline composition.
  • the amine-acid adducts are particularly useful in highly volatile fuels having a Reid vapor pressure above about 9 which are particularly prone to engine stalling due to ice formation under cool, humid conditions.
  • the additive of the invention is particularly useful in winter gasolines employed in northern portions of the country since they have Reid vapor pressures between about 9 and 13.5, depending on the area.
  • a preferred class of effective amine-acid adducts have the general formula: RNH R'COOH wherein R is an aliphatic hydrocarbyl radical containing 218 carbon atoms and R is an aliphatic hydrocarbyl radical containing 1-17 carbon atoms, the total number of carbon atoms in said adduct being between 8 and 20.
  • Arnine-monocarboxylic acid adducts are usually solids and are simply prepared by mixing equi-molar portions of a C to C aliphatic hydrocarbyl monocarboxylic acid with an aliphatic amine containing 2-18 carbon atoms and having a pka between 8 and 11.5.
  • Aliphatic hydrocarbyl amines containing 2-18 carbon atoms have high base strengths as measured by a pka between 8 and 11.5 so that they readily form stable adducts with aliphatic hydrocarbyl monocarboxylic acids containing 218 carbon atoms.
  • pka is defined as the negative log of the acid ionization constant.
  • the amine-acid adduct It is necessary for the amine-acid adduct to have a total of 8 to 20 carbon atoms to be effective as an antistalling, anti-icing additive. As will be shown later, adducts containing either below 8 or above 20 carbon atoms are relatively ineffective as anti-stalling, anti-icing additives.
  • Examples of effective anti-stalling, anti-icing amineacid adducts are the following: ethylamine-lauric acid adduct, ethylamine-Z-ethylhexanoic acid adduct, isopropylamine-Z-ethylhexanoic acid adduct, isopropylaminemyristic acid adduct, hexylamine-propionic acid adduct, nonylamine-acetic acid adduct, nonylamine-Z-ethylhexanoic acid adduct, laurylamine-propionic acid adduct, laurylamine-hexanoic acid adduct and laurylamine-butyric acid adduct.
  • the amine-acid adducts are effective as anti-stalling, anti-icing additives in concentrations of 0.001 to 0.05 weight percent of the total fuel.
  • Adduct concentrations as high as 0.1 weight percent can be employed but lower concentrations falling within the preferred 0.001 to 0.02 weight percent concentration range are just as effective from the standpoint of imparting anti-stalling, anti-icing properties to gasoline.
  • carburetor icing demonstrator apparatus consisting of a single cylinder Briggs and Stratton engine equipped so that cooled, moisture-saturated air from an ice tower is drawn through a simple glass tube gasoline carburetor and fed into the engine.
  • the gasoline sample is placed in a sample bottle and is drawn into the glass carburetor through a hypodermic needle which is usually 20 gauge. Evaporation of the gasoline in the glass tube further cools the cold, moist air with resulting ice formation on the throttle plate.
  • the formation of ice on the throttle plate causes the engine to stall and the time required for the engine to stall due to ice formation is recorded and serves as a measure of the icing and stalling properties of the fuel being tested.
  • the engine is run at 3500 rpm. because this engine speed has been found to be best for differentiating between the icing and stalling properties of different fuels. Since most fuels stall in 1-4- minutes, 300 seconds is the maximum time for a run. A recording of 300 seconds indicates no stall within the test period. Each fuel is run four times in succession and the average is reported. If the differences between runs are great, the glass tube carburetor and test throttle are washed with alcohol and the runs repeated.
  • a leaded winter grade premium gaso'line having a Reid vapor pressure of about 13 gives a stall in about 45-55 seconds in this test.
  • Additives which raise the stalling time to over seconds and preferably over 200 seconds are regarded as effective anti-stalling, anti-icing additives.
  • the base fuel employed to evaluate the effectivenesses of amine-monocarboxylic acid adducts of prescribed composition as anti-stalling anti-icing additives for gasoline was a winter grade premium gasoline having an octane rating of about 100 and containing 3 cc. of TEL per gallon.
  • This winter grade gasoline which had a 50% ASTM distillation point of 2 10 and a Reid vapor pressure of about 13 lbs., was ideally suited for testing the stalling characteristics of the additives because of its high vapor pressure.
  • This base fuel had an average stalling time of 47 seconds in the afore-described stalling test.
  • Isopentanoic acid 76 Propionic acid 60 Isooctane soluble fraction of a wax oxidate 60 t-Butyl amine 46 Primene 81R (a ec -C alkyl primary amine) 6 1 Primene J MT (a LC -C alkyl amine) 46
  • the data in the foregoing table demonstrate that the hydrocarbyl monocarboxylic acids and high base strength amines in concentrations of 16 lbs/1000 bbls. of fuel equivalent to a concentration of 0.006 weight percent, have substantially no effect on the anti-stalling, anti-icing properties of the base fuel.
  • Table 11 there is shown the action of various amineacid adducts as anti-stalling, anti-icing additives in the same base fuel employed in Table I.
  • amineacid adducts containing less than 8 or more than 20 carbon atoms only slightly improve the anti-stalling properties of the base fuel.
  • a good anti-icing, anti-stalling additive should improve the properties of the base fuel to such an extent that no stall is noted in 200* seconds.
  • a gasoline motor fuel having a Reid vapor pressure above 9 and containing 0.001 to 0.05 weight percent of an amine-acid adduct having the general formula:
  • R is an aliphatic hydrocarbyl radical containing 2-18 carbon atoms and R is an aliphatic hydrocarbyl radical containing 1-17 carbon atoms, said adduct containing a total of 8-20 carbon atoms and imparting improved anti-stalling, anti-icing properties to said motor fuel.

Description

United States Patent 3,055,746 ADDUCTS 0F ALIPHATKC MONOCARBQXYLIC ACIDS AND ALIPHATIC AMINES IN GASfJLHIE George W. Eckert, Wappingers Falls, N.Y., assignor to Texaco Inc., New York, N.Y., a corporation of Delaware No Drawing. Filed May 7, 1959, Ser. No. 811,535 9 Claims. (Cl. 4466) This invention relates to a volatile gasoline composition of improved anti-stalling properties containing an adduct of a monocarboXylic acid and a high base strength amine of prescribed composition. More particularly, it involves the discovery that adducts of monocarboxylic acids and high base strength amines are effective antistalling additives for gasoline.
In a commonly-assigned copending application, Serial No. 803,385, filed April 1, 1959, it is disclosed that adducts of a high base strength amine and a C to C hydrocarbyl monocarboxylic acid in a concentration between about 0.2 and 5.0 weight percent act as octane appreciators for leaded gasoline having a prescribed aromatic and/or olefin content. The subject invention involves the discovery that adducts of hydrocarbyl monocarboxylic acids and high base strength amines of prescribed chain length are effective anti-stalling and anti-icing additives for volatile gasolines in substantially lower concentrations than are required for their actions as octane appreciators.
The gasoline fuel composition of this invention comprises a substan ial concentration of volatile components, and 0.001 to 0.1 weight percent of an adduct of a C to C alkyl amine having a pka between 8 and 11.5 and a hydrocarbyl monocarboxylic acid containing 2 to 18 carbon atoms, said adduct containing a total of 8 to 20 carbon atoms. The presence of amine-acid adducts of prescribed composition and in prescribed concentration imparts outstanding anti-icing and anti-stalling properties to the resulting gasoline composition.
When internal combustion engines are operated on a gasoline fuel having the desired volatility characteristics for cold weather driving, a sta'lling problem is encountered during the warm-up period, particularly under cool, humid atmospheric conditions. It has been generally recognized that the cause of repeated engine stalling in cool, humid 'weather is the formation of ice in the carburetor. Gasoline evaporating in the carburetor has a sufficient refrigerating effect to condense and freeze moisture present in the air. Ice particles deposit on the metal surfaces of the carburetor and partially or completely block the air passage between the carburetor throat and the carburetor throttle valve with resulting stalling, particularly when the engine is idling. The amine-acid adducts are particularly useful in highly volatile fuels having a Reid vapor pressure above about 9 which are particularly prone to engine stalling due to ice formation under cool, humid conditions. Stated another way, the additive of the invention is particularly useful in winter gasolines employed in northern portions of the country since they have Reid vapor pressures between about 9 and 13.5, depending on the area.
A preferred class of effective amine-acid adducts have the general formula: RNH R'COOH wherein R is an aliphatic hydrocarbyl radical containing 218 carbon atoms and R is an aliphatic hydrocarbyl radical containing 1-17 carbon atoms, the total number of carbon atoms in said adduct being between 8 and 20.
Arnine-monocarboxylic acid adducts are usually solids and are simply prepared by mixing equi-molar portions of a C to C aliphatic hydrocarbyl monocarboxylic acid with an aliphatic amine containing 2-18 carbon atoms and having a pka between 8 and 11.5. Aliphatic hydrocarbyl amines containing 2-18 carbon atoms have high base strengths as measured by a pka between 8 and 11.5 so that they readily form stable adducts with aliphatic hydrocarbyl monocarboxylic acids containing 218 carbon atoms. In Physical Chemistry, by Daniels and A1- berti, published in 1955 by John Wiley & Sons, pages 466-471, pka is defined as the negative log of the acid ionization constant. A pka of 7 and particularly a pka of 8 and above, indicates a high base strength, whereas a pka below 7 indicates low base strength.
It is necessary for the amine-acid adduct to have a total of 8 to 20 carbon atoms to be effective as an antistalling, anti-icing additive. As will be shown later, adducts containing either below 8 or above 20 carbon atoms are relatively ineffective as anti-stalling, anti-icing additives.
Examples of effective anti-stalling, anti-icing amineacid adducts are the following: ethylamine-lauric acid adduct, ethylamine-Z-ethylhexanoic acid adduct, isopropylamine-Z-ethylhexanoic acid adduct, isopropylaminemyristic acid adduct, hexylamine-propionic acid adduct, nonylamine-acetic acid adduct, nonylamine-Z-ethylhexanoic acid adduct, laurylamine-propionic acid adduct, laurylamine-hexanoic acid adduct and laurylamine-butyric acid adduct.
The amine-acid adducts are effective as anti-stalling, anti-icing additives in concentrations of 0.001 to 0.05 weight percent of the total fuel. Adduct concentrations as high as 0.1 weight percent can be employed but lower concentrations falling within the preferred 0.001 to 0.02 weight percent concentration range are just as effective from the standpoint of imparting anti-stalling, anti-icing properties to gasoline. Concentrations of the order of 4 and 16 lbs. of adduct per 1000 bbls. of gasoline equivalent to concentrations of 0.0015 and 0.006 weight percent, respectively, have proven particularly effective in forming fuels of excellent anti-stalling properties.
The action of the adducts as anti-stalling, anti-icing additives was evaluated in carburetor icing demonstrator apparatus consisting of a single cylinder Briggs and Stratton engine equipped so that cooled, moisture-saturated air from an ice tower is drawn through a simple glass tube gasoline carburetor and fed into the engine. The gasoline sample is placed in a sample bottle and is drawn into the glass carburetor through a hypodermic needle which is usually 20 gauge. Evaporation of the gasoline in the glass tube further cools the cold, moist air with resulting ice formation on the throttle plate. The formation of ice on the throttle plate causes the engine to stall and the time required for the engine to stall due to ice formation is recorded and serves as a measure of the icing and stalling properties of the fuel being tested. The engine is run at 3500 rpm. because this engine speed has been found to be best for differentiating between the icing and stalling properties of different fuels. Since most fuels stall in 1-4- minutes, 300 seconds is the maximum time for a run. A recording of 300 seconds indicates no stall within the test period. Each fuel is run four times in succession and the average is reported. If the differences between runs are great, the glass tube carburetor and test throttle are washed with alcohol and the runs repeated. A leaded winter grade premium gaso'line having a Reid vapor pressure of about 13 gives a stall in about 45-55 seconds in this test. Additives which raise the stalling time to over seconds and preferably over 200 seconds are regarded as effective anti-stalling, anti-icing additives.
The base fuel employed to evaluate the effectivenesses of amine-monocarboxylic acid adducts of prescribed composition as anti-stalling anti-icing additives for gasoline was a winter grade premium gasoline having an octane rating of about 100 and containing 3 cc. of TEL per gallon. This winter grade gasoline, which had a 50% ASTM distillation point of 2 10 and a Reid vapor pressure of about 13 lbs., was ideally suited for testing the stalling characteristics of the additives because of its high vapor pressure. This base fuel had an average stalling time of 47 seconds in the afore-described stalling test.
In Table I there is shown the effect of individual acids and amines on the stalling properties of this base fuel.
TABLE I Base fuel 16 lbs. additive per 1000 bb1s.:
Stalling time, secs.
Isopentanoic acid 76 Propionic acid 60 Isooctane soluble fraction of a wax oxidate 60 t-Butyl amine 46 Primene 81R (a ec -C alkyl primary amine) 6 1 Primene J MT (a LC -C alkyl amine) 46 The data in the foregoing table demonstrate that the hydrocarbyl monocarboxylic acids and high base strength amines in concentrations of 16 lbs/1000 bbls. of fuel equivalent to a concentration of 0.006 weight percent, have substantially no effect on the anti-stalling, anti-icing properties of the base fuel.
In Table 11 there is shown the action of various amineacid adducts as anti-stalling, anti-icing additives in the same base fuel employed in Table I.
TABLE II Action of Amine-Acid Adducts as Anti-Icing Additives Concen- Stalling Additive tration, Time,
Weight secs. Percent Adducts containing 8-20 carbon atoms:
t-butylamine: 2-ethy1l1exanoic acid 0. 006 300+ 0. 003 258+ 0. 0015 8 c. atoms) 0.006 241 Primene 81Rzpropionic acid (av. 16 0.
atoms) 0. 006 300+ t-butylammezlsopentanoic acid 0. 006 279+ t-butylaminezisooctane soluble fraction of wax oxidate (est. av. of 20 c. atoms). 0. 006 200 D 0. 0015 203 t-butylaminczisooctane soluble fraction of oxidized SAE 8 paraflin distillate oil (est. av. of 18 c. atoms) 0.006 243 n-butylamine:2ethylhexanoic acid 0. 006 271 Adducts Containing less than 8 Carbon Atomst-butylamine:propionic acid 0. 006 85 Adduets Containing more than 20 Carbon Atoms:
Primene .TMTz2ethylhexanolc acid (est.
av. of 28 0. atoms) 0.006 85 D0 0.0015 72 Primene JMTzisopentanoic acid (est. av.
of 25 0. atoms) 0. 006 87 Primene J MTzpropionic acid (est. av. of
23 0. atoms) 0.006 118 Primene .IMTzisooctane soluble wax oxidate traction (est. av. of 36 0. atoms).. 0.006 74 Primene .IMTzisooctane soluble fraction of oxidized SAE 8 parafiin base distillate (est. av. of 34 0. atoms) O. 006 111 Primene 81Rz2-ethylhexanoie acid (est.
av. of 21 0. atoms) 0.006 61 Primene 81R: isooctane soluble fraction of oxidized SAE 8 paraffin base distillate (est. av. of 27 0. atoms) 0. 006 131 The data in the foregoing table prove conclusively the outstanding superiority of acid-amine adducts containing 8-20 carbon atoms as anti-stalling, anti-icing additives in comparison with adducts containing both a smaller and higher number of carbon atoms in the molecule. Amineacid adducts of the prescribed number of carbon atoms in the molecule all significantly improve the anti-stalling properties of the base fuel from a level of 47 seconds to over 200 seconds for the first stall. In contrast, amineacid adducts containing less than 8 or more than 20 carbon atoms only slightly improve the anti-stalling properties of the base fuel. As has been indicated previously, a good anti-icing, anti-stalling additive should improve the properties of the base fuel to such an extent that no stall is noted in 200* seconds.
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.
I claim:
1. A gasoline containing 0.001 to 0.1 weight percent of an adduct having the general formula RNH -R'COOH wherein R is an aliphatic hydrocarbyl radical containing 2-18 carbon atoms and R is an aliphatic hydrocarbyl radical containing 1-17 carbon atoms, said adduct containing a total of 23-20 carbon atoms and imparting improved anti-stalling, anti-icing properties to said gasoline.
2. The gasoline according to claim 1 having a Reid vapor pressure above about 9.
3. The gasoline according to claim 1 in which said amine-acid adducts are present in a concentration between 0.001 and 0.05 weight percent.
4. A gasoline motor fuel having a Reid vapor pressure above 9 and containing 0.001 to 0.05 weight percent of an amine-acid adduct having the general formula:
wherein R is an aliphatic hydrocarbyl radical containing 2-18 carbon atoms and R is an aliphatic hydrocarbyl radical containing 1-17 carbon atoms, said adduct containing a total of 8-20 carbon atoms and imparting improved anti-stalling, anti-icing properties to said motor fuel.
5. The gasoline motor fuel according to claim 4 in which said adduct is a t-butylamine:2-ethylhexanoic acid adduct.
6. The gasoline motor fuel according to claim 4 in which said adduct is t-butylamine:isopentanoic acid adduct.
7. The gasoline motor fuel according to claim 4 in which said adduct is an n-butylamine:Z-ethylheikanoic acid adduct.
8. The gasoline motor fuel according to claim 4 in which said adduct is a t-C to C alkyl primary amine: propionic acid adduct.
9. The gasoline motor fuel according to claim 4 in which said adduct is a t-C to C alkyl primary amine: isopentanoic acid adduct.
References Cited in the file of this patent UNITED STATES PATENTS 2,330,524 Shields Sept. 28, 1934 2,430,951 Rouault Nov. 18, 1947 2,629,649 Wachter et al Feb, 24, 1953 2,861,874 OKelly et al Nov. 25, 1958 2,883,276 Larsen Apr. 21, 1959 2,902,353 Becker et al Sept. 1, 1959 2,915,528 Raifsnider Dec. 1, 1959 OTHER REFERENCES Improved Motor Fuels Through Selective Blending, by Wagner et a1., November 7, 1941, pp. 8-13.
Petroleum Refining With Chemicals, Kalichevsky and Kobe, 1956, p. 480.

Claims (1)

1. A GASOLINE CONTAINING 0.001 TO 0.1 WEIGHT PERCENT OF AN ADDUCT HAVING THE GENERAL FORMULA RNH2 R''COOH WHEREIN R IS AN ALIPHATIC HYDROCARBYL RADICAL CONTAINING 2-18 CARBON ATOMS AND R'' IS AN ALIPHATIC HYDROCARBYL RADICAL CONTAINING 1-17 CARBON ATOMS, SAID ADDUCT CONTAINING A TOTAL OF 8-20 CARBON ATOMS AND IMPARTING IMPROVED ANTI-STALLING, ANTI-ICING PROPERTIES TO SAID GASOLINE.
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Cited By (8)

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US3256074A (en) * 1962-11-13 1966-06-14 Texaco Inc Anti-stalling motor fuel
US3473902A (en) * 1965-08-26 1969-10-21 Texaco Inc Fuel composition
US3534075A (en) * 1968-03-05 1970-10-13 Mobil Oil Corp Liquid hydrocarbon compositions containing amine salts of ethylene diamine tetra acetic acid as antistatic agents
FR2563839A1 (en) * 1984-05-01 1985-11-08 Bank Of America Motor fuels contg. alcohol
EP0829527A1 (en) * 1996-09-12 1998-03-18 Exxon Research And Engineering Company Additive concentrate for fuel compositions
EP1357170A2 (en) * 2002-04-24 2003-10-29 Ethyl Corporation Friction modifier additives for fuel compositions and methods of use thereof
US20040010966A1 (en) * 2002-04-24 2004-01-22 Aradi Allen A. Additives for fuel compositions to reduce formation of combustion chamber deposits
US20070094921A1 (en) * 2002-04-24 2007-05-03 William Colucci Methods to improve the low temperature compatibility of amide friction modifiers in fuels and amide friction modifiers

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US2883276A (en) * 1954-01-21 1959-04-21 Phillips Petroleum Co Fuel containing anti-icing additives
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US2915528A (en) * 1956-05-28 1959-12-01 Shell Dev Perfluoroalkylimidazolines

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US2330524A (en) * 1941-06-16 1943-09-28 Alox Corp Corrosion inhibitor
US2430951A (en) * 1943-11-27 1947-11-18 Standard Oil Co Corrosion inhibiting compositions
US2629649A (en) * 1949-10-31 1953-02-24 Shell Dev Vapor-phase corrosion inhibitor
US2883276A (en) * 1954-01-21 1959-04-21 Phillips Petroleum Co Fuel containing anti-icing additives
US2861874A (en) * 1954-06-23 1958-11-25 Alox Corp Corrosion inhibitor for light petroleum solvents and fuels
US2915528A (en) * 1956-05-28 1959-12-01 Shell Dev Perfluoroalkylimidazolines
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Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3256074A (en) * 1962-11-13 1966-06-14 Texaco Inc Anti-stalling motor fuel
US3473902A (en) * 1965-08-26 1969-10-21 Texaco Inc Fuel composition
US3534075A (en) * 1968-03-05 1970-10-13 Mobil Oil Corp Liquid hydrocarbon compositions containing amine salts of ethylene diamine tetra acetic acid as antistatic agents
FR2563839A1 (en) * 1984-05-01 1985-11-08 Bank Of America Motor fuels contg. alcohol
US6277158B1 (en) 1996-09-12 2001-08-21 Exxon Research And Engineering Company Additive concentrate for fuel compositions
WO1998011175A1 (en) * 1996-09-12 1998-03-19 Exxon Research And Engineering Company Additive concentrate for fuel compositions
EP0829527A1 (en) * 1996-09-12 1998-03-18 Exxon Research And Engineering Company Additive concentrate for fuel compositions
EP1357170A2 (en) * 2002-04-24 2003-10-29 Ethyl Corporation Friction modifier additives for fuel compositions and methods of use thereof
US20030200697A1 (en) * 2002-04-24 2003-10-30 Aradi Allen A. Friction modifier additives for fuel compositions and methods of use thereof
US20040010966A1 (en) * 2002-04-24 2004-01-22 Aradi Allen A. Additives for fuel compositions to reduce formation of combustion chamber deposits
EP1357170A3 (en) * 2002-04-24 2004-09-08 Ethyl Corporation Friction modifier additives for fuel compositions and methods of use thereof
US20070094921A1 (en) * 2002-04-24 2007-05-03 William Colucci Methods to improve the low temperature compatibility of amide friction modifiers in fuels and amide friction modifiers
US7402185B2 (en) 2002-04-24 2008-07-22 Afton Chemical Intangibles, Llc Additives for fuel compositions to reduce formation of combustion chamber deposits
US7846224B2 (en) 2002-04-24 2010-12-07 Afton Chemical Intangibles, Llc Methods to improve the low temperature compatibility of amide friction modifiers in fuels and amide friction modifiers
EP1462506A1 (en) * 2003-03-26 2004-09-29 Ethyl Corporation Additives for fuel compositions to reduce formation of combustion chamber deposits

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