US2776194A - Gasoline compositions - Google Patents

Gasoline compositions Download PDF

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US2776194A
US2776194A US430745A US43074554A US2776194A US 2776194 A US2776194 A US 2776194A US 430745 A US430745 A US 430745A US 43074554 A US43074554 A US 43074554A US 2776194 A US2776194 A US 2776194A
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gasoline
additive
oil
engine
hours
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Walter W Scheumann
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Cities Service Research and Development Co
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Cities Service Research and Development Co
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M1/00Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
    • C10M1/08Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
    • 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
    • C10L1/16Hydrocarbons
    • C10L1/1608Well defined compounds, e.g. hexane, benzene
    • 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
    • C10L1/16Hydrocarbons
    • C10L1/1616Hydrocarbons fractions, e.g. lubricants, solvents, naphta, bitumen, tars, terpentine
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/182Organic compounds containing oxygen containing hydroxy groups; Salts thereof
    • C10L1/1822Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms
    • C10L1/1824Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms mono-hydroxy
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/188Carboxylic acids; metal salts thereof
    • C10L1/1881Carboxylic acids; metal salts thereof carboxylic group attached to an aliphatic carbon atom
    • C10L1/1883Carboxylic acids; metal salts thereof carboxylic group attached to an aliphatic carbon atom polycarboxylic 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, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/22Organic compounds containing nitrogen
    • C10L1/222Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
    • C10L1/223Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond having at least one amino 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
    • C10L1/22Organic compounds containing nitrogen
    • C10L1/23Organic compounds containing nitrogen containing at least one nitrogen-to-oxygen bond, e.g. nitro-compounds, nitrates, nitrites
    • C10L1/231Organic compounds containing nitrogen containing at least one nitrogen-to-oxygen bond, e.g. nitro-compounds, nitrates, nitrites nitro compounds; nitrates; nitrites
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/02Well-defined aliphatic compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/02Well-defined aliphatic compounds
    • C10M2203/022Well-defined aliphatic compounds saturated
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/02Well-defined aliphatic compounds
    • C10M2203/024Well-defined aliphatic compounds unsaturated
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/04Well-defined cycloaliphatic compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/021Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
    • C10M2207/123Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms polycarboxylic
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/129Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/22Acids obtained from polymerised unsaturated acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/20Containing nitrogen-to-oxygen bonds

Definitions

  • This invention relates to an improved compound additive for gasoline and to gasolines containing the additive, andmore particularly to an additive composition effective to reduce engine deposits and piston ring wear when in corporated into a gasoline.
  • dimer acid the dimerized linoleic acid being prepared according to the directions given in Journal of American Oil Chemists Society 24,65 March, 1947. This acid will be hereinafter referred to as dimer acid.
  • I may increase the percentage of isopropyl alcohol to about 50%, and for winter driving to about 70%, decreasing the percentages of the other ingredients proportionately. In such cases, however, I increase the amount of additive so as to maintain in the gasoline approximately the same concentration of ingredients other than alcohol as when using 0.5% 'of additive A.
  • the total time on each test was 60 hours of continuous operation divided into hourly no-load and 5.4 B. H. P. load cycles.
  • Rusting tests were also carried out on gasoline containing 0.5% additive A. These tests were carried out under ASTM D-665 test procedure using synthetic sea water with the following modifications.
  • test pieces immersed in gasoline containing 0.5% of additive A did not develop incipient rusting until a period of 68 hours had elapsed, whereas the average time to develop incipient rusting in test pieces exposed to a reference gasoline was 14 hours.
  • a gasoline containing from about 0.25 to about 2 percent by volume of a composition comprising the following ingredients in the range of proportions set forth, all percentages being by volume.
  • a gasoline containing about 0.5% by volume of a composition comprising the following ingredients in ap proximately the proportions set forth, all percentages being by volume.

Description

United States Patent GASOLINE COMPOSITIONS Walter W. Scheumann, Cranford, N. J., assignor to Cities Service Research and Development Company, New York, N. Y., a corporation of New Jersey No Drawing. Application May 18, 1954, Serial No. 430,745
2 Claims. (Cl. 44-56) This invention relates to an improved compound additive for gasoline and to gasolines containing the additive, andmore particularly to an additive composition effective to reduce engine deposits and piston ring wear when in corporated into a gasoline.
This application is a continuation-impart of my application S. N. 345,830, filed March 31, 1953, and now abandoned.
I have discovered that the performance of gasoline in respect of engine cleanliness and piston ring wear may be significantly improved by the addition thereto, in small but significant amounts, usually in the order of A to 2 percent of a composition containing the following ingredients:
Volume Percent Light solvent refined hydrocarbon lubricating oil (100 S. U. S. 100 F.) 25-80 Benzol 4-12 Isopropyl alcohol -70 Dimerized linoleic acid 0.2-0.6 Dihexyl phenyl amine 0.2-0.7 Amyl nitrate 0.03-0.15
the dimerized linoleic acid being prepared according to the directions given in Journal of American Oil Chemists Society 24,65 March, 1947. This acid will be hereinafter referred to as dimer acid.
While the ingredients may be mixed together in the above proportions, and added to a gasoline in the amounts specified, I have found that for summer driving, good results may be obtained by adding to a gasoline 0.5% of an additive having the following composition:
For spring or fall I may increase the percentage of isopropyl alcohol to about 50%, and for winter driving to about 70%, decreasing the percentages of the other ingredients proportionately. In such cases, however, I increase the amount of additive so as to maintain in the gasoline approximately the same concentration of ingredients other than alcohol as when using 0.5% 'of additive A.
Gasolines containing 0.25% and 0.5% of additive A have been extensively tested for piston ring Wear, combustion chamber deposits, and rusting characteristics.
In determining the effect of the additive on piston ring wear, tests were conducted in a Chevrolet engine under EL-2 conditions except for the following modifications.
(a) The top compression rings for cylinders 1, 2, 3, 4,
and 5 were exposed to 3x10 neutrons per cm. per second flux for a period of one week in an atomic pile. Five hot rings were used in order to make the test as sensitive to wear as possible. A greater number were not used because five were considered to be the maximum number that could be safely handled.
(b) The engine was converted to run with a dry sump to facilitate flushing, reduce the oil charge required, and make possible continuous radioactive sampling throughout the test.
(c) The engine was operated under the following conditions.
Test duration, hours 10 Brake H. P 25 R. P. M 2500:20 Water outle't temperature, "F :5 Water inlet temperature, "F 90:2 Lube oil temperature, "F :5 Air-fuel ratio 14.5 :1 Exhaust back pressure (in. water) l3.6:7.8 Ignition timing 38:3 BTC .The standard radioactive tracer technique was used. As the radioactive piston rings wore, the particles were suspended in the lubricating oil and the level of radioactivity recorded by a Geiger tube immersed in a constant volume of oil that was circulating through the system.
Final evaluation of the wear of each run was obtained by calculating the slopes of the wear curves during the last six hours and the last nine hours. The first part of each curve reflected the high wear rate coincident with a cold start under these conditions, the last six hours reflected a stable wear rate. Carry-over effect between each test was minimized by flushing first with a mixture of solvent and oil, and then with oil only.
An average of five tests on a reference gasoline indicated an average rise per hour in counts per minute for the last nine hours of 1014, and a rise for the last 6 hours of 973. When using the same reference gasoline, with 0.5 of additive A added, an average of four tests showed the rise for the last nine hours to be 952, and for the last 6 hours 868. It is felt that the 4 to 10 hour average is a more accurate yardstick than the 1 to 10 hour average, and this indicates that the additive fuel gives in the neighborhood of 10 percent less wear under the test conditions used.
In testing for engine cleanliness characteristics two sets of runs were made to compare the effects of a reference gasoline with gasoline containing 0.25% and 0.5 additive A in a Chevrolet engine. Before the start of each run the engine was flushed with a solvent, torn down, cleaned, reassembled, and filled with SAE 20 oil. The oil level was checked every 8 hours during the runs, and more oil was added as needed. At the conclusion of each run the engine head was removed, and the deposits were scraped from the top of the pistons and surrounding fiat surface block areas and placed in crucibles. Oil and soluble products of combustion were removed by repeated washings with benzene. The deposits were then dried and Weighed on an analytical balance. To determine the amount of ash, the crucibles were placed in a muffle, ashed, and reweighed.
The total time on each test was 60 hours of continuous operation divided into hourly no-load and 5.4 B. H. P. load cycles.
Results of the tests indicated that 0.25% of additive A resulted in a reduction of 6.7% in oil free deposits, while the addition of 0.5 of additive A resulted in a reduction of 13.5% in oil free deposits, and 24.8% in ash.
A series of road tests were also run in a 1952 DeSoto passenger car, using reference gasoline, and a gasoline containing 0.5 of additive A. It was found that use of the additive reduced oil free deposits by 14%, and ash by 30%.
Rusting tests were also carried out on gasoline containing 0.5% additive A. These tests were carried out under ASTM D-665 test procedure using synthetic sea water with the following modifications.
(a) The test duration was increased until incipient rus'ting was experienced.
(b) The temperature was reduced from 140 to room temperature.
Means were employed for replacing the gasoline lost by evaporation.
(d) The R. P. M. of the stirrer was reduced to 800 R. P. M.
It was found that under these conditions the test pieces immersed in gasoline containing 0.5% of additive A did not develop incipient rusting until a period of 68 hours had elapsed, whereas the average time to develop incipient rusting in test pieces exposed to a reference gasoline was 14 hours.
The reason why my new additive should be so succesful in reducing wear and engine deposits is not known, since the various ingredients, with the exception of the lubricating oil, are present in the treated gasoline in such minute amounts that it could scarcely be believed that they would be of any value whatever. The addition of the small quantity of lubricating oil specified might be expected to decrease piston wear to a minor extent, but then only at a penalty of increased engine deposits due to cracking and incomplete combustion of the oil in the cylinder. As demonstrated, however, contrary to expectations the engine deposits are decreased rather than increased. Ithas also been noted that the engine deposits formed when using :a gasoline treated with my additive are different in character from those formed when using untreated gasoline, being granular and easily removed from the various engine parts, whereas the deposits formed when using untreated gasoline are varnish like and removable only with difficulty.
It has been found that the octane number of the gasoline is not affected in any way by the incorporation of my additive in the recommended amounts. This would also appear to be surprising, since amyl nitrate is used as a cetane improver in diesel fuels, and would normally be expected to have a detrimental effect on the octane number. It is speculated that the other ingredients of the additive must in some way neutralize the adverse effects of amyl nitrate or-. octane number, while preserving its useful characteristics in the composition.
Having now described my invention, what is claimed is:
1. A gasoline containing from about 0.25 to about 2 percent by volume of a composition comprising the following ingredients in the range of proportions set forth, all percentages being by volume.
Percent Solvent refined light hydrocarbon lubricating oil S. U. S. at 100 F.) 25-80 Benzol 4-12 Isopropyl alcohol 10-70 Dimerized linoleic acid 0.2-0.6 Dihexyl phenyl amine 0.2-0.7
Amyl nitrate 0.03-0.l5
2. A gasoline containing about 0.5% by volume of a composition comprising the following ingredients in ap proximately the proportions set forth, all percentages being by volume.
References Cited in the file of this patent UNITED STATES PATENTS 2,324,779 Kass July 20, 1943 2,413,262 Stirton Dec. 24, 1946 2,632,695 Landis et a1 Mar. 24, 1953 2,646,348 Neudeck July 21, 1953

Claims (1)

1. A GASOLINE CONTAINING FROM ABOUT 0.25 TO ABOUT 2 PERCENT BY VOLUME OF A COMPOSITION COMPRISING THE FOLLOWING INGREDIENTS IN THE RANGE OF PROPORTIONS SET FORTH, ALL PERCENTAGES BEING BY VOLUME. SOLVENT REFINED LIGHT HYDROCARBON LUBRICATING
US430745A 1954-05-18 1954-05-18 Gasoline compositions Expired - Lifetime US2776194A (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2914479A (en) * 1955-04-26 1959-11-24 Standard Oil Co Upper cylinder lubricant and tune-up solvent composition
US3303007A (en) * 1963-09-03 1967-02-07 Union Oil Co Motor fuel composition
EP0313696A1 (en) * 1987-10-28 1989-05-03 Mobil Oil Corporation Diesel fuel with improved cetane number and containing polynitrate esters and stabilizers

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2324779A (en) * 1940-07-25 1943-07-20 Standard Oil Dev Co Motor fuel
US2413262A (en) * 1943-05-10 1946-12-24 Union Oil Co High-compression motor fuel
US2632695A (en) * 1951-09-20 1953-03-24 Socony Vacuum Oil Co Inc Rust inhibitor for light petroleum products
US2646348A (en) * 1951-12-15 1953-07-21 Standard Oil Dev Co Gasoline fuels containing dimethyl carbinol and solvent oil

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2324779A (en) * 1940-07-25 1943-07-20 Standard Oil Dev Co Motor fuel
US2413262A (en) * 1943-05-10 1946-12-24 Union Oil Co High-compression motor fuel
US2632695A (en) * 1951-09-20 1953-03-24 Socony Vacuum Oil Co Inc Rust inhibitor for light petroleum products
US2646348A (en) * 1951-12-15 1953-07-21 Standard Oil Dev Co Gasoline fuels containing dimethyl carbinol and solvent oil

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2914479A (en) * 1955-04-26 1959-11-24 Standard Oil Co Upper cylinder lubricant and tune-up solvent composition
US3303007A (en) * 1963-09-03 1967-02-07 Union Oil Co Motor fuel composition
EP0313696A1 (en) * 1987-10-28 1989-05-03 Mobil Oil Corporation Diesel fuel with improved cetane number and containing polynitrate esters and stabilizers

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