US2938776A - Distillate fuel composition - Google Patents

Distillate fuel composition Download PDF

Info

Publication number
US2938776A
US2938776A US504087A US50408755A US2938776A US 2938776 A US2938776 A US 2938776A US 504087 A US504087 A US 504087A US 50408755 A US50408755 A US 50408755A US 2938776 A US2938776 A US 2938776A
Authority
US
United States
Prior art keywords
carbon
aluminum
gasoline
glow
lead
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
US504087A
Inventor
Hamer Martin
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.)
Standard Oil Co
Original Assignee
Standard Oil Co
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
Application filed by Standard Oil Co filed Critical Standard Oil Co
Priority to US504087A priority Critical patent/US2938776A/en
Application granted granted Critical
Publication of US2938776A publication Critical patent/US2938776A/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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/1814Chelates
    • 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/188Carboxylic acids; metal salts thereof
    • C10L1/1886Carboxylic acids; metal salts thereof naphthenic acid
    • 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/26Organic compounds containing phosphorus
    • C10L1/2608Organic compounds containing phosphorus containing a phosphorus-carbon bond
    • 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/26Organic compounds containing phosphorus
    • C10L1/2633Organic compounds containing phosphorus phosphorus bond to oxygen (no P. C. bond)
    • C10L1/2641Organic compounds containing phosphorus phosphorus bond to oxygen (no P. C. bond) oxygen bonds only
    • 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/26Organic compounds containing phosphorus
    • C10L1/2633Organic compounds containing phosphorus phosphorus bond to oxygen (no P. C. bond)
    • C10L1/265Organic compounds containing phosphorus phosphorus bond to oxygen (no P. C. bond) oxygen and/or sulfur bonds
    • 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/26Organic compounds containing phosphorus
    • C10L1/2691Compounds of uncertain formula; reaction of organic compounds (hydrocarbons acids, esters) with Px Sy, Px Sy Halz or sulfur and phosphorus 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • 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

  • My invention relates to improvements in the suppression of surface ignition of leaded gasolines in the operation of internal combustion engines. More particularly, my invention provides a novel additive combination, which incorporated in gasoline, is effective in suppression of surface ignition.
  • an additive combination essentially comprising an oil soluble aluminum compound and an oil soluble phosphorus compound is provided.
  • the additive combination is made up in the form of a concentrate in a solvent oil vehicle. The concentrate then may be conveniently added in small quantities to finished gasolines containing tetraethyl lead,
  • the relative properties of the aluminum containing and phosphorus containing components are desirably se- 2,938,776 Patented May 31, 1960' lected to provide approximately equimolar proportions of aluminum oxide (A1 0 and phosphorus pentoxido (P 0 upon combustion. These proportions, however, can be varied considerably, say from about 90 parts of one to 10 parts of the other, while retaining the benefits of the invention.
  • the additive combination may be made up in any suitable solvent oil facilitating blending into finished gasoline, for example, naphtha, light gas oil, catalytic cycle oil, light lubricating oil fractions, or aromatic solvents such as benzene, toluene, xylenes and the like.
  • the additive may be blended into leaded gasoline, usually containing from about 1 to 3 ccs.-of tetraethyl lead per gallon in concentrations from about 0.0001 to 0.1 weight percent of the additive on an oil free basis.
  • the invention is applied with the greatest advantage to premium motor gasolines, which usually boil in the 100 to 350 F. range, but it may be employed with broader cut gasolines and even fuels of somewhat higher boiling.
  • a particularly convenient form for the phosphorus component is tricresyl phosphate since it has desirable oil solubility and is available on a commercial scale.
  • Other oil soluble phosphorus compounds such as tris-chloropropyl thionophosphate, the dialkyl dithiophosphites and various trialkyl and triaryl phosphates, phosphites and phosphonates have value.
  • finished gasoline blends ordinarily contain other additives such as anti-oxidants, gum inhibitors, anti-rusts and dyes, the compatibility of the aluminum and phosphorus compounds used according to the invention with these additives should be considered.
  • phosphorus compounds containing sulfur may be somewhat less desirable than those that are sulfur free because of the deleterious effect of sulfur on the lead response of the gasoline stock, that is to improvement in Octane number by addition of tetraethyl lead.
  • the effectiveness of aluminum and lead in reducing the glow of combustion chamber deposits was evaluated on a bench scale by determining the glow point, or 10 second ignition delay temperature, of the sample under examination. The test was carried out by placing the sample of either carbon or combustion chamber deposit +additive on a stainless steel dish which had been heated in an open pot type furnace to a specified temperature.
  • the temperature was indicated by means of a thermocouple which was placed inside a well extending from the outside to the center of the sample dish.
  • the time required for visible glow (ignition) of the sample to occur was measured by means of a stopwatch. That temperature at which the sample glowed 10 seconds after being placed on the steel dish was recorded as the glow point.
  • Carbon- +Pb (PO No glow at 1130. Carbon +Al O No glow at 1130. Carbon- +A12O3.P2O5 NO glOW at Carbon +PbCl 800; Carbon-+PbCl +Pb (PO 800. Carbon Carboh-l-PbCl +Al O .P O 1000.
  • Example I leaded gasoline containing 3.0 cc. per gallon of TEL was inhibited by the addition of tricresyl phosphate, using 0.1 mol of that theoretically required for reaction with the tetraethyl lead when the mixture' isburned' in the combustion chamber, and 0.0375 percent byweight of aluminum naphthenate.
  • the additive combination of the invention was found to efiect a substantial reduction in preignition, together with a decrease in the normal octane requirement increase.
  • Example 11 In this example, the eifect of the phosphorus and aluminum compounds used separately was compared to the use of the additive combination.
  • the fuel was a leaded gasoline containing 3.0 cc. per gallon of tetracthyl lead.
  • tabl e re sults with the base fuel are tabulated in column 1 results-with the base fuel con- '-taining tricresyl phosphate in an amount equiyalent to e4 of that theoretically required to form lead phosphate in -the'combustion chamber 'are tabulated in column' 2;
  • a distillate fuel comprising a major proportion of gasoline containing tetraethyl lead and a minor proportion of an additive combination essentially comprisingessentially comprises from. about 10 to parts of aluminum naphthenate, from about 10 to 90 parts of tria cresyl phosphate, and a sufiicientamount of a solvent oil to provide fluidity.

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 F DISTILLATE FUEL COMPOSITION Martin Hamer, Chicago, 111., assignor to Standard Oil Company, Chicago, 11]., a corporation of Indiana No Drawing. Filed Apr. 26, 1955, Ser. No. 504,087
2 Claims. (CI. 44-69) My invention relates to improvements in the suppression of surface ignition of leaded gasolines in the operation of internal combustion engines. More particularly, my invention provides a novel additive combination, which incorporated in gasoline, is effective in suppression of surface ignition.
Current emphasis on high compression ratios, and other high performance design features, in gasoline engines of the internal combustion type has tended to raise not only octane requirements but has created a situation where knock from surface ignition, often referred to as preignition, has become a limiting factor in engine design and operation. Knock induced by surface ignition appears to be a concomitant of the use of tetraethyl lead as the anti-knock agent in fuels of high performance value. When motor fuels containing tetraethyl lead are burned in internal combustion engines, deposits consisting of carbonaceous material and lead salts are continuously formed in the combustion chambers. These deposits are harmful in that they increase the octane requirement of the engine by inducing knock and causing preignition. Apparently preignition, that is the ignition of the fuel charge before passage of the spark, is caused by glowing of the carbon in the deposits. Moreover, lead salts are known to cause carbon to glow at a significantly lower temperature than the glow point of carbon alone.
I have discovered that the presence of aluminum and phosphorus in the combustion chamber suppresses the glowing of carbon; i.e., increases the glow point, and hence acts to suppress knock induced by surface ignition. According to my invention, an additive combination essentially comprising an oil soluble aluminum compound and an oil soluble phosphorus compound is provided. Advantageously, the additive combination is made up in the form of a concentrate in a solvent oil vehicle. The concentrate then may be conveniently added in small quantities to finished gasolines containing tetraethyl lead,
thus providing. finished gasoline blends inhibited against.
knock induced by surface ignition.
I have found, in the course of my investigations, that it is essential to provide the combination of aluminum and phosphorus in the combustion chamber if suppression of knock by surface ignition is to be significantly controlled. 1 have also'found that the nature of the aluminum compound does not appear to be controlling, provided that it is sufliciently oil soluble for use in gasoline, since control tests have shown that aluminum oxide appears to be the effective factor in raising carbon glow point. It is believed that, in the engine, any oil soluble, organic aluminum compound is converted to aluminum oxide. Similarly, I have found that the criterion of utility for the phosphorus component is oil solubility to an extent permitting its use in gasoline rather than the particular nature of any particular phosphorus compound.
In producing the additive combination of the invention, the relative properties of the aluminum containing and phosphorus containing components are desirably se- 2,938,776 Patented May 31, 1960' lected to provide approximately equimolar proportions of aluminum oxide (A1 0 and phosphorus pentoxido (P 0 upon combustion. These proportions, however, can be varied considerably, say from about 90 parts of one to 10 parts of the other, while retaining the benefits of the invention. The additive combination may be made up in any suitable solvent oil facilitating blending into finished gasoline, for example, naphtha, light gas oil, catalytic cycle oil, light lubricating oil fractions, or aromatic solvents such as benzene, toluene, xylenes and the like. The additive may be blended into leaded gasoline, usually containing from about 1 to 3 ccs.-of tetraethyl lead per gallon in concentrations from about 0.0001 to 0.1 weight percent of the additive on an oil free basis.
The invention is applied with the greatest advantage to premium motor gasolines, which usually boil in the 100 to 350 F. range, but it may be employed with broader cut gasolines and even fuels of somewhat higher boiling.
A particularly convenient form for the phosphorus component is tricresyl phosphate since it has desirable oil solubility and is available on a commercial scale. Other oil soluble phosphorus compounds such as tris-chloropropyl thionophosphate, the dialkyl dithiophosphites and various trialkyl and triaryl phosphates, phosphites and phosphonates have value. It should be noted that because finished gasoline blends ordinarily contain other additives such as anti-oxidants, gum inhibitors, anti-rusts and dyes, the compatibility of the aluminum and phosphorus compounds used according to the invention with these additives should be considered. Also, phosphorus compounds containing sulfur may be somewhat less desirable than those that are sulfur free because of the deleterious effect of sulfur on the lead response of the gasoline stock, that is to improvement in Octane number by addition of tetraethyl lead. V
The effectiveness of aluminum and lead in reducing the glow of combustion chamber deposits was evaluated on a bench scale by determining the glow point, or 10 second ignition delay temperature, of the sample under examination. The test was carried out by placing the sample of either carbon or combustion chamber deposit +additive on a stainless steel dish which had been heated in an open pot type furnace to a specified temperature.
The temperature was indicated by means of a thermocouple which was placed inside a well extending from the outside to the center of the sample dish. The time required for visible glow (ignition) of the sample to occur was measured by means of a stopwatch. That temperature at which the sample glowed 10 seconds after being placed on the steel dish was recorded as the glow point.
In extensive glow point testing it was determined that although lead phosphate, presumably the end product of an organic phosphorus compound in the combustion chamber, reduces the glow point of pure carbon, it is ineffective in reducing the glow of either carbon plus lead chloride, presumably present from decomposition of tetraethyl lead, or of actual combustion chamber deposits. On the other hand, it was found that the combination of aluminum oxide, presumably the end product only pure carbon but also carbon plus leadchloride and actualcombustion chamber deposits; The illustrative data-are-tabulatedbelow:
' 10 sec. ignition delay temp. F.)
Carbonalone 1130.
Carbon- +Pb (PO No glow at 1130. Carbon +Al O No glow at 1130. Carbon- +A12O3.P2O5 NO glOW at Carbon +PbCl 800; Carbon-+PbCl +Pb (PO 800. Carbon Carboh-l-PbCl +Al O .P O 1000.
Combustion chamber deposit alone 730. Combustion chamber deposit ;+Pu P0,) 750. Combustion chamber deposit ;+A1,o, 750. Combustion chamber deposit Q+AI O .P O 840.
an additive combination, illustrative of the invention, was evaluated in a Pontiac engine using a cycled-load procedure under the following operating conditions:
once an hour a Duration 45 sec. 135 sec Q93 2%? Cycle Engine Speed. 700 r.p.m. 2,000 r.p.m throttle accelr oad none 26 lbs eration for 30 see.
Compression ratio 7.6:1. AirFuel ratio- As found. Test duration 150 hours. Coolant temp 1605 F. Oil Tempo l65=l=10 F.
Example I In this example, leaded gasoline containing 3.0 cc. per gallon of TEL was inhibited by the addition of tricresyl phosphate, using 0.1 mol of that theoretically required for reaction with the tetraethyl lead when the mixture' isburned' in the combustion chamber, and 0.0375 percent byweight of aluminum naphthenate. In tests with a 1953 Pontiac S-cylinder engine using a 165 hour cycled load procedure under the above conditions, the additive combination of the invention was found to efiect a substantial reduction in preignition, together with a decrease in the normal octane requirement increase. The
Example 11 In this example, the eifect of the phosphorus and aluminum compounds used separately was compared to the use of the additive combination. The fuel was a leaded gasoline containing 3.0 cc. per gallon of tetracthyl lead. In the following tabl e, re sults with the base fuel are tabulated in column 1 results-with the base fuel con- '-taining tricresyl phosphate in an amount equiyalent to e4 of that theoretically required to form lead phosphate in -the'combustion chamber 'are tabulated in column' 2;
results with the additive combinatiomusing 0.1 theoretical unit of tricresyl phosphate and 1 an equimolar proportion of aluminum naphthenate, are tabulated in column 3; and results with the base fuel containing aluminum naphthenate alone in an amount equivalent to the amount of tricresyl phosphate as in column 2 are tabulated in column 4. The tests were conducted with a 1953 Pontiac engine in a manner similar to thatof Example I. It will be noted fromthetabulated data 'that the use of the additive combination produceda significant reduction in preignitioncount and octane requirement increase whereas the use ofeitherofthe components separately peared tobe relatively ineifective.
Preignition Count .Q 147 102 50 115 OBI 5.0 3.5 2.0 5.0 Total Deposit (g.) 94.4 97.3 93.2 90.0
I claim: r 1. A distillate fuel comprising a major proportion of gasoline containing tetraethyl lead and a minor proportion of an additive combination essentially comprisingessentially comprises from. about 10 to parts of aluminum naphthenate, from about 10 to 90 parts of tria cresyl phosphate, and a sufiicientamount of a solvent oil to provide fluidity.
References Cited in the file of this patent UNITED STATES PATENTS 2,086,775

Claims (1)

1. A DISTILLATE FUEL COMPRISING A MAJOR PROPORTION GASOLINE CONTAINING TETRAETHYL LEAD AND A MINOR PROPORTION OF AN ADDITIVE COMBINATION ESSENTIALLY COMPRISING FROM ABOUT 10 TO 90 PARTS OF ALUMINUM NAPHTHENATE AND FROM ABOUT 10 TO PARTS OF TRICESYL PHOSPHATE, SAID ADDITIVE COMBINATION BEING IN AN AMOUNT SUFFICIENT TO REDUCE SUSCEPTIBILITY OF THE LEADED GASOLINE TO SURFACE IGNITION.
US504087A 1955-04-26 1955-04-26 Distillate fuel composition Expired - Lifetime US2938776A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US504087A US2938776A (en) 1955-04-26 1955-04-26 Distillate fuel composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US504087A US2938776A (en) 1955-04-26 1955-04-26 Distillate fuel composition

Publications (1)

Publication Number Publication Date
US2938776A true US2938776A (en) 1960-05-31

Family

ID=24004791

Family Applications (1)

Application Number Title Priority Date Filing Date
US504087A Expired - Lifetime US2938776A (en) 1955-04-26 1955-04-26 Distillate fuel composition

Country Status (1)

Country Link
US (1) US2938776A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3073852A (en) * 1960-09-30 1963-01-15 California Research Corp Bis (trimethyllead) sulfide
US3073853A (en) * 1960-09-30 1963-01-15 California Research Corp Trimethyl lead methyl sulfide
US3097225A (en) * 1960-09-12 1963-07-09 Ethyl Corp Acetylenic nickel compounds

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR684887A (en) * 1929-02-12 1930-07-02 Chimiotherapie Lab Franc Improvements in fuel mixtures for explosion engines
US2086775A (en) * 1936-07-13 1937-07-13 Leo Corp Method of operating an internal combustion engine
US2405560A (en) * 1943-02-06 1946-08-13 Gen Motors Corp Fuel
US2427173A (en) * 1944-03-29 1947-09-09 Gen Motors Corp Fuel
US2451345A (en) * 1944-10-24 1948-10-12 Standard Oil Dev Co Compounded lubricating oil
US2534217A (en) * 1948-04-06 1950-12-19 Standard Oil Co Lubricant comprising reaction product of an olefin, a phosphorus sulfide, and water
US2599341A (en) * 1947-10-29 1952-06-03 Standard Oil Dev Co New phosphorus containing compounds
FR1100185A (en) * 1953-11-05 1955-09-16 Ethyl Corp Improvements relating to anti-knock agents for fuels and their manufacturing processes
US2739049A (en) * 1951-10-04 1956-03-20 Exxon Research Engineering Co Gasoline type fuel composition

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR684887A (en) * 1929-02-12 1930-07-02 Chimiotherapie Lab Franc Improvements in fuel mixtures for explosion engines
US2086775A (en) * 1936-07-13 1937-07-13 Leo Corp Method of operating an internal combustion engine
US2405560A (en) * 1943-02-06 1946-08-13 Gen Motors Corp Fuel
US2427173A (en) * 1944-03-29 1947-09-09 Gen Motors Corp Fuel
US2451345A (en) * 1944-10-24 1948-10-12 Standard Oil Dev Co Compounded lubricating oil
US2599341A (en) * 1947-10-29 1952-06-03 Standard Oil Dev Co New phosphorus containing compounds
US2534217A (en) * 1948-04-06 1950-12-19 Standard Oil Co Lubricant comprising reaction product of an olefin, a phosphorus sulfide, and water
US2739049A (en) * 1951-10-04 1956-03-20 Exxon Research Engineering Co Gasoline type fuel composition
FR1100185A (en) * 1953-11-05 1955-09-16 Ethyl Corp Improvements relating to anti-knock agents for fuels and their manufacturing processes

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3097225A (en) * 1960-09-12 1963-07-09 Ethyl Corp Acetylenic nickel compounds
US3073852A (en) * 1960-09-30 1963-01-15 California Research Corp Bis (trimethyllead) sulfide
US3073853A (en) * 1960-09-30 1963-01-15 California Research Corp Trimethyl lead methyl sulfide

Similar Documents

Publication Publication Date Title
US2405560A (en) Fuel
US1692784A (en) Fuel and fuel ingredients
US2797153A (en) Fuel for spark ignition internal combustion engines
US2427173A (en) Fuel
US2158050A (en) Motor fuel
US3009791A (en) Liquid hydrocarbons containing a boron additive
CA1306868C (en) Gasoline fuel composition
US2938776A (en) Distillate fuel composition
US3707362A (en) Method and composition for optimizing air-fuel ratio distribution in internal combustion engines
US2324779A (en) Motor fuel
US2863743A (en) Motor fuel
US2833635A (en) Gasoline fuel
US3305330A (en) Amine-phosphorus-containing adducts and motor fuel containing same
US3020137A (en) Motor fuel compositions
US3009797A (en) Boron-containing jet fuel compositions
US3052528A (en) Gasoline composition
US2931714A (en) Motor gasoline containing boron and hexylene glycol
US3733184A (en) Composition for improving air-fuel ratio distribution in internal combustion engines
US2994595A (en) Motor fuel compositions
US2980520A (en) Gasoline motor fuel
US3056667A (en) Leaded gasoline containing phosphorus and phosphate
US3560174A (en) Motor fuel composition
US3418091A (en) Tetramethyllead and arylphosphate gasoline composition
US3047374A (en) Motor fuel compositions
US3070430A (en) Combustion chamber deposit modifiers for leaded gasolines