US2324779A - Motor fuel - Google Patents
Motor fuel Download PDFInfo
- Publication number
- US2324779A US2324779A US347484A US34748440A US2324779A US 2324779 A US2324779 A US 2324779A US 347484 A US347484 A US 347484A US 34748440 A US34748440 A US 34748440A US 2324779 A US2324779 A US 2324779A
- Authority
- US
- United States
- Prior art keywords
- fuel
- ignition
- motor
- agents
- knock
- 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
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Classifications
-
- 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
-
- 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
- C10L1/23—Organic compounds containing nitrogen containing at least one nitrogen-to-oxygen bond, e.g. nitro-compounds, nitrates, nitrites
- C10L1/231—Organic compounds containing nitrogen containing at least one nitrogen-to-oxygen bond, e.g. nitro-compounds, nitrates, nitrites nitro compounds; nitrates; nitrites
-
- 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
- C10L1/30—Organic compounds compounds not mentioned before (complexes)
- C10L1/305—Organic compounds compounds not mentioned before (complexes) organo-metallic compounds (containing a metal to carbon bond)
- C10L1/306—Organic compounds compounds not mentioned before (complexes) organo-metallic compounds (containing a metal to carbon bond) organo Pb compounds
Definitions
- Relatively heavy motor fuels containing low volatility ends are of high calorific value but have tendencies to cause fuming and objectionable odor in exhaust gases when used in sparkignition type engines. These combustion product difliculties are very annoying and, nevertheless, very commonly accompany the operation of internal combustionengines used in large motor vehicles, as; for example, trucks and motor buses,
- the objects of this invention are to improve motor fuels in their combustion performance by addition agents which effectively accomplish a reduction in fuming and odor without seriously detracting from anti-knock qualities and power output of the fuel so that the fuel may retain its economical and practical value.
- organo-metallic compounds such as lead alltyl anti-knock'agents, and certain ignition accelerating agents, when added in combination of small proportions to the motor fuels, accomplish the aforesaid objects.
- Substances having ignition acceleration effects which have been discovered to be well adapted for utilization in the present respects comprise preferably organic nitrates, and, more particularly, alkyl nitrates containing from 3 to 6 carbon atoms per molecule as, for example, isopropyl nitrate, butyl nitrates, amyl nitrate and iso-amyl nitrate.
- organic peroxides, nitrogen derivatives, and organic sulfides of similar molecular weight, volatility, and ignition accelerating'properties are used.
- the substances are in common characterized as being aliphatic compounds containing oxygen, nitrogen, and/or sulfur in an active form, but furthermore, for the objects of this invention, .
- the compounds of this general class are preferably tion of the odor in the exhaust gases; and in keeping with the object of avoiding reduction in the fuel performance, the preferred types of ignition accelerator agents remarkably avoid. depression of the anti-knock value of the fuel.
- the following tabulated results illustrate that the ignition accelerator does not adversely affect the octane number of the leaded fuel; and therefore can be economically employed in such fuels to accomplish the objects of this invention.
- Gasoline base 65 a s2. 0 Gasoline base+0.014% amyl nitrate 62. l 82. 1 Gasoline base+0.2% 'amyl nitrate 57.1 79. o
- the addition agents are added to a hydrocarbon fuel base generally boiling within the range of 100 F. to 450 F., but the fuel base may have an end point as high as 500 F. or even 600 F.
- the fuel base may be of the nature of a straight run gasoline or naphtha, and it may be a motor fuel distillate fraction obtained by any of the commercial conversion processes, such as thermal cracking, reforming, catalytic cracking, or destructive hydrogenation.
- the fuel base may also have incorporated various high octane blending value fuel ingredients, such as are obtained by proc esses of alkylation, polymerization, and hydrogenation.
- anti-knock blending agents such as isopropyl ether, aniline, benzol, etc.
- the quantity of the ignition accelerator agent to be added to the fuel .5 restricted as much as possible consistent with obtaining the desired improvement in the combustion, and generally this amount is between the approximate limits of 0.005% to 0.2% by weight, of the fuel composition.
- the lead alkyl anti-knock agent employed, together with the ignition accelerator, may be used in amounts ranging from 0.5 cc. to 5 cc. per
- additives blended with the fuel for improving the combustion qualities may also include various synthetic
- various other types of blending agents may be used, such as materials having lubricating or gum fluxing properties, .dyes, corrosion inhibitors, antioxidants, color stabilizing agents, etc.
- a motor fuel for spark-ignition engines comprising a gasoline base fuel blended with from 0.5 cc. to 5 cc. per gallon of lead alkyl antlknock agent, and with from 0.005% to 0.2%, by weight of the fuel composition, of an alkyl nitrate containing from 3 to 6 carbon atoms per molecule.
- composition as described in claim 1 in which said alkyl nitrate as amyl nitrate.
- a motor fuel comprising essentially gasoline, about 3 cc. per gallon of tetraethyl lead, and about 014% of amyl nitrate, said fuel being substantially free from tendency to form fumes and objectionable exhaust odors during use in a spark-ignition engine.
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
Patented July 20, 1943 MOTOR FUEL Charles B. Kass, Elizabeth, N. J., assignor to Standard Oil Development Company, a corporation of Delaware No Drawing. Application July 25, 1940,
Serial'hlo. 347,484
3Claims. (Cl. 44-69) selected when they have boiling points within This invention relate to motor fuels and particularly to a method of improving their combus-,
tion in spark-ignition engines.
Relatively heavy motor fuels containing low volatility ends are of high calorific value but have tendencies to cause fuming and objectionable odor in exhaust gases when used in sparkignition type engines. These combustion product difliculties are very annoying and, nevertheless, very commonly accompany the operation of internal combustionengines used in large motor vehicles, as; for example, trucks and motor buses,
which for economical reasons use relatively heavy motor fuels. The same situation exists to a lesser but still annoying degree with motor fuels of conventional volatility.
The objects of this invention are to improve motor fuels in their combustion performance by addition agents which effectively accomplish a reduction in fuming and odor without seriously detracting from anti-knock qualities and power output of the fuel so that the fuel may retain its economical and practical value.
It has been found that substances having high anti-knock or detonation properties, in particular, organo-metallic compounds such as lead alltyl anti-knock'agents, and certain ignition accelerating agents, when added in combination of small proportions to the motor fuels, accomplish the aforesaid objects.
Although there are a large number of subthe range of 100 C. to 300" C.
Using the preferred types of ignition acceler-' ating agents, incorporated in very minute proportions into an ordinary commercial gasoline, or a motor fuel of relatively heavy character, such as is sometimes used in heavily constructed internal combustion engines of the spark-ignition type, theobjectionable nature of the exhaust gas has been very successfully eliminated. It has been found of additionalsignificance, that when the fuels are also blended with small .amounts of a lead alkyl, anti-knock agent, the results have been even better with respect to the reducstances which have the property of accelerating of the present invention, because a number of them detrimentally tend, to cause excessive preignition, also, a number of them excessively lower the anti-knock and calorifiic values of the fuel, or in other ways interfere with the improvement desired.
Substances having ignition acceleration effects which have been discovered to be well adapted for utilization in the present respects comprise preferably organic nitrates, and, more particularly, alkyl nitrates containing from 3 to 6 carbon atoms per molecule as, for example, isopropyl nitrate, butyl nitrates, amyl nitrate and iso-amyl nitrate. Next in order to these maybe used organic peroxides, nitrogen derivatives, and organic sulfides of similar molecular weight, volatility, and ignition accelerating'properties. The substances are in common characterized as being aliphatic compounds containing oxygen, nitrogen, and/or sulfur in an active form, but furthermore, for the objects of this invention, .the compounds of this general class are preferably tion of the odor in the exhaust gases; and in keeping with the object of avoiding reduction in the fuel performance, the preferred types of ignition accelerator agents remarkably avoid. depression of the anti-knock value of the fuel.
The following example and test data will further illustrate the nature and advantages of this invention: i
Example the trial runs without causing any detectable Further tests were made with a C. F. R. engine to determinemore accuratelythe eflects of the ignition accelerating agents on the anti-knock value of the fuels. The following tabulated results illustrate that the ignition accelerator does not adversely affect the octane number of the leaded fuel; and therefore can be economically employed in such fuels to accomplish the objects of this invention.
A. S. 'l. M. I octane number I Fuel composition 3 cc. Clear '1. E. L.
Gasoline base 65. a s2. 0 Gasoline base+0.014% amyl nitrate 62. l 82. 1 Gasoline base+0.2% 'amyl nitrate 57.1 79. o
In the practice of this invention the addition agents are added to a hydrocarbon fuel base generally boiling within the range of 100 F. to 450 F., but the fuel base may have an end point as high as 500 F. or even 600 F. The fuel base may be of the nature of a straight run gasoline or naphtha, and it may be a motor fuel distillate fraction obtained by any of the commercial conversion processes, such as thermal cracking, reforming, catalytic cracking, or destructive hydrogenation. The fuel base may also have incorporated various high octane blending value fuel ingredients, such as are obtained by proc esses of alkylation, polymerization, and hydrogenation. anti-knock blending agents, such as isopropyl ether, aniline, benzol, etc.
The quantity of the ignition accelerator agent to be added to the fuel .5 restricted as much as possible consistent with obtaining the desired improvement in the combustion, and generally this amount is between the approximate limits of 0.005% to 0.2% by weight, of the fuel composition. The lead alkyl anti-knock agent employed, together with the ignition accelerator, may be used in amounts ranging from 0.5 cc. to 5 cc. per
gallon of the fuel.
It may also include various synthetic In addition to the additives blended with the fuel for improving the combustion qualities, various other types of blending agents may be used, such as materials having lubricating or gum fluxing properties, .dyes, corrosion inhibitors, antioxidants, color stabilizing agents, etc.
It is desired not to be limited by any of the specific examples given for the sake of illustration, and various modifications may be made within the scope of the appended claims.
I claim: 1
l. A motor fuel for spark-ignition engines, comprising a gasoline base fuel blended with from 0.5 cc. to 5 cc. per gallon of lead alkyl antlknock agent, and with from 0.005% to 0.2%, by weight of the fuel composition, of an alkyl nitrate containing from 3 to 6 carbon atoms per molecule.
2. A composition as described in claim 1, in which said alkyl nitrate as amyl nitrate.
3. A motor fuel comprising essentially gasoline, about 3 cc. per gallon of tetraethyl lead, and about 014% of amyl nitrate, said fuel being substantially free from tendency to form fumes and objectionable exhaust odors during use in a spark-ignition engine.
CHARLES B. KASS.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US347484A US2324779A (en) | 1940-07-25 | 1940-07-25 | Motor fuel |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US347484A US2324779A (en) | 1940-07-25 | 1940-07-25 | Motor fuel |
Publications (1)
Publication Number | Publication Date |
---|---|
US2324779A true US2324779A (en) | 1943-07-20 |
Family
ID=23363886
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US347484A Expired - Lifetime US2324779A (en) | 1940-07-25 | 1940-07-25 | Motor fuel |
Country Status (1)
Country | Link |
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US (1) | US2324779A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2645079A (en) * | 1944-06-06 | 1953-07-14 | Union Oil Co | Method of operating jet propulsion motors |
DE953480C (en) * | 1950-04-19 | 1956-11-29 | British Petroleum Co | Fuel mixture for two-stroke engines |
US2776194A (en) * | 1954-05-18 | 1957-01-01 | Cities Service Res & Dev Co | Gasoline compositions |
DE1005313B (en) * | 1954-03-17 | 1957-03-28 | British Petroleum Co | Fuel for four-stroke engines |
US4240801A (en) * | 1979-05-31 | 1980-12-23 | Ethyl Corporation | Diesel fuel composition |
US5405417A (en) * | 1990-07-16 | 1995-04-11 | Ethyl Corporation | Fuel compositions with enhanced combustion characteristics |
US5782937A (en) * | 1997-05-19 | 1998-07-21 | Ethyl Corporation | Gasoline compositions containing ignition improvers |
EP1371715A1 (en) * | 2002-06-13 | 2003-12-17 | Shell Internationale Researchmaatschappij B.V. | Fuel compositions |
-
1940
- 1940-07-25 US US347484A patent/US2324779A/en not_active Expired - Lifetime
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2645079A (en) * | 1944-06-06 | 1953-07-14 | Union Oil Co | Method of operating jet propulsion motors |
DE953480C (en) * | 1950-04-19 | 1956-11-29 | British Petroleum Co | Fuel mixture for two-stroke engines |
DE1005313B (en) * | 1954-03-17 | 1957-03-28 | British Petroleum Co | Fuel for four-stroke engines |
US2776194A (en) * | 1954-05-18 | 1957-01-01 | Cities Service Res & Dev Co | Gasoline compositions |
US4240801A (en) * | 1979-05-31 | 1980-12-23 | Ethyl Corporation | Diesel fuel composition |
US5405417A (en) * | 1990-07-16 | 1995-04-11 | Ethyl Corporation | Fuel compositions with enhanced combustion characteristics |
US5782937A (en) * | 1997-05-19 | 1998-07-21 | Ethyl Corporation | Gasoline compositions containing ignition improvers |
EP0879871A1 (en) * | 1997-05-19 | 1998-11-25 | Ethyl Corporation | Gasoline compositions containing ignition improvers |
EP1371715A1 (en) * | 2002-06-13 | 2003-12-17 | Shell Internationale Researchmaatschappij B.V. | Fuel compositions |
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