US1907309A - Liquid fuel - Google Patents
Liquid fuel Download PDFInfo
- Publication number
- US1907309A US1907309A US412568A US41256829A US1907309A US 1907309 A US1907309 A US 1907309A US 412568 A US412568 A US 412568A US 41256829 A US41256829 A US 41256829A US 1907309 A US1907309 A US 1907309A
- Authority
- US
- United States
- Prior art keywords
- alcohol
- gasoline
- alcohols
- tertiary
- liquid fuel
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000446 fuel Substances 0.000 title description 18
- 239000007788 liquid Substances 0.000 title description 8
- 235000019441 ethanol Nutrition 0.000 description 29
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 20
- 239000003502 gasoline Substances 0.000 description 20
- 150000001298 alcohols Chemical class 0.000 description 10
- 239000003209 petroleum derivative Substances 0.000 description 9
- 238000002156 mixing Methods 0.000 description 8
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 7
- 150000003509 tertiary alcohols Chemical class 0.000 description 7
- 150000003333 secondary alcohols Chemical class 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 238000002485 combustion reaction Methods 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 2
- -1 aliphatic alcohols Chemical class 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical group C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- KFSYJTMPRJSZHA-UHFFFAOYSA-N 1-(2-methylbutan-2-yloxy)pentane Chemical group CCCCCOC(C)(C)CC KFSYJTMPRJSZHA-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 125000005909 ethyl alcohol group Chemical group 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
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
- C10L1/18—Organic compounds containing oxygen
- C10L1/182—Organic compounds containing oxygen containing hydroxy groups; Salts thereof
- C10L1/1822—Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms
- C10L1/1824—Organic compounds containing oxygen containing hydroxy groups; Salts thereof hydroxy group directly attached to (cyclo)aliphatic carbon atoms mono-hydroxy
-
- 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
- C10L1/02—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
- C10L1/023—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only for spark ignition
Definitions
- This invention relates to a liquid fuel that is suitable .for use in internal combustion engines and that comprises an alcohol of calorific value that is relatively high in proportion to its boiling point.
- Alcohols have been suggested and used for some time as an addition to gasoline for automobile and other internal combustion engines. Ethyl alcohol has been the most used.
- tertiary alcohols By using secondary or tertiary alcohols in mixed motor fuels, I combine the desir able, relatively high vapor pressure with other desirable properties of alcohols of higher molecular weight.
- Particularly suitable alcohols for use in liquid fuels are isopropyl, secondary or tertiary butyl, and tertiary amyl.
- tertiary butyl alcohol has nearly the same calorific value as butyl alcohol (primary butanol) on the one hand IVhile the higher alcohols are pref-' Application filed December 7, 1929'. Serial no. 412,568.
- he secondary or tertiary alcohols may be mixed with petroleum distillate, as, for example, naphtha, gasoline, or kerosene, in various proportions.
- petroleum distillate as, for example, naphtha, gasoline, or kerosene, in various proportions.
- I have used to advantage 10 to 40 volumes of the secondary or tertiary alcohol, say 30, with suflicient petroleum distillate to make a total of 100 volumes.
- tertiary butyl parts ethyl dimethyl density of 58 to 60 B. Or it may be of a lower density, say of an average of approximately 64 B. Petroleum distillate that is more volatile than the usual motor gasoline is particularly desirable when the alcohol used is secondary butyl, tertiary amyl (ethyl dimethyl carbinol), or a less volatile secondary or tertiary alcohol.
- aqueous alcohols containing, for example, up to 12% of water.
- a blending agent such as ether, a ketone, or benzol.
- the moisture which separates on mixing the wet alcohol with the petroleum distillate without a blending agent may be separated, in whole or in part, as, by centrifugal action, settling, passing through a layer of a salt, such as anhydrous sodium sulfate; the resulting oil layer may then serve as a liquid fuel without a blending agent.
- a salt such as anhydrous sodium sulfate
- Blends of secondary and/or tertiary alcohols with petroleum distillates have desirable and useful properties.
- motor fuels decrease knocking in the motor.
- a motor which could be made to knock with either so-called ethyl gasoline or with a blend of 30 volumes of benzol to of gasoline did not knock with a. fuel comprising 30 volumes of tertiary butyl alcohol and 70 of U. S. motor gasoline.
- a fuel comprising 10 volumes of tertiary butyl alcohol and 90 of gasoline knocked less than the same gasoline without the addition of tertiary butyl alcohol.
- composition suitable for use as a fuel consisted of 20 or 25 volumes of secondary and /or tertiary aliphatic alcohols to 80 or of gasoline or other petroleum distillate. Further, the blends of secondary and /or tertiary alcohols, particularly of tertiary butyl alcohol, with a petroleum distillate are useful as solvents for certain oils and waxes.
- a liquid fuel consisting of a petroleum distillate and a tertiary aliphatic alcohol.
- a liquid fuel consisting of gasoline and tertiary butyl alcohol.
- a motor fuel consisting of approximately 75 volumes of gasoline and 25 of tertiary butyl alcohol.
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)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Liquid Carbonaceous Fuels (AREA)
Description
Patented May 2, 1933 UNITED STATES PATENT OFFICE ROBERT H. VAN SCHAACK,
JR., OF EVANSTON, ILLINOIS, ASSIGNOR TO VAN SCHAACK BROS. CHEMICAL WORKS, INC.,'OF CHICAGO, ILLINOIS, A CORPORATION OF ILLINOIS LIQUID FUEL a No Drawing.
This invention relates to a liquid fuel that is suitable .for use in internal combustion engines and that comprises an alcohol of calorific value that is relatively high in proportion to its boiling point.
Alcohols have been suggested and used for some time as an addition to gasoline for automobile and other internal combustion engines. Ethyl alcohol has been the most used.
There are a number of objections to the use of alcohol in such fuels. If the alcohol is low boiling and, therefore, most suitable in vapor pressure for use in gasoline then the alcohol has a much lower calorific value than the gasoline. This is particularly true of the methyl and ethyl alcohols. Further, there is difliculty of blending gasoline with low boiling alcohols, unless the alcohols are nearly anhydrous or unless there is used a blending agent. Numerous blending agents are disclosed in the patent literature.
In the series of monohydric, aliphatic alcohols, the heat of combustion per mole and also per gram increases with the molecular Weight of the alcohol. Also, the distribumixtures for motors,
- tion coetficient of the alcohol in gasoline and Water solutions indicates a higher solubility of the alcohol in the hydrocarbon layer, the higher the molecular weight of the al cohol. erable to ethyl alcohol in these regards, many of the higher alcohols have vapor pressures that are lower than desired for certain motor fuels. Thus propyl and butyl alcoholsby these terms I mean the primary alcoholshave lower vapor pressures than ethyl alcohol at atmospheric temperatures.
By using secondary or tertiary alcohols in mixed motor fuels, I combine the desir able, relatively high vapor pressure with other desirable properties of alcohols of higher molecular weight. Particularly suitable alcohols for use in liquid fuels are isopropyl, secondary or tertiary butyl, and tertiary amyl. Thus, tertiary butyl alcohol has nearly the same calorific value as butyl alcohol (primary butanol) on the one hand IVhile the higher alcohols are pref-' Application filed December 7, 1929'. Serial no. 412,568.
and, on the other, nearly the same evaporation rate as ethyl alcohol.
he secondary or tertiary alcohols may be mixed with petroleum distillate, as, for example, naphtha, gasoline, or kerosene, in various proportions. I have used to advantage 10 to 40 volumes of the secondary or tertiary alcohol, say 30, with suflicient petroleum distillate to make a total of 100 volumes.
Examples of motor fuel compositions follow. All proportions, here and elsewhere in this application, are expressed as parts by volume.
1. Gasoline, -90 parts; isopropyl alcohol, 40-10 parts.
2. Gasoline, 60-90 parts; alcohol, 40-10 parts.
3. Gasoline, 60-90 parts; secondary butyl alcohol, 40-10 parts.
4. Gasoline, 60-90 carbinol, 40-10 parts.
tertiary butyl parts; ethyl dimethyl density of 58 to 60 B. Or it may be of a lower density, say of an average of approximately 64 B. Petroleum distillate that is more volatile than the usual motor gasoline is particularly desirable when the alcohol used is secondary butyl, tertiary amyl (ethyl dimethyl carbinol), or a less volatile secondary or tertiary alcohol.
In view of the readiness with which most of the water may be separated from aqueous secondary and tertiary alcohols, I suitably use these alcohols in a partly dried condition for blending with the motor fuel. I prefer to dry the alcohol so thoroughly that it will withstand, without forming a cloud of precipitated water, dilution with gasoline in a proportion somewhat larger than the proportion that is to be used in the finished liquid fuel. I may dry alcohol until it contains, for example, less than 2%, say 1%, of Water.
As an alternative to this drying of the alcohols before use, I may use aqueous alcohols containing, for example, up to 12% of water. \Vhen these are mixed with a petroleum distillate there is used a blending agent, such as ether, a ketone, or benzol. Or,
the moisture which separates on mixing the wet alcohol with the petroleum distillate without a blending agent may be separated, in whole or in part, as, by centrifugal action, settling, passing through a layer of a salt, such as anhydrous sodium sulfate; the resulting oil layer may then serve as a liquid fuel without a blending agent.
Blends of secondary and/or tertiary alcohols with petroleum distillates have desirable and useful properties. motor fuels. As such they decrease knocking in the motor. Thus, a motor which could be made to knock with either so-called ethyl gasoline or with a blend of 30 volumes of benzol to of gasoline did not knock with a. fuel comprising 30 volumes of tertiary butyl alcohol and 70 of U. S. motor gasoline. Likewise, a fuel comprising 10 volumes of tertiary butyl alcohol and 90 of gasoline knocked less than the same gasoline without the addition of tertiary butyl alcohol. Another composition suitable for use as a fuel consisted of 20 or 25 volumes of secondary and /or tertiary aliphatic alcohols to 80 or of gasoline or other petroleum distillate. Further, the blends of secondary and /or tertiary alcohols, particularly of tertiary butyl alcohol, with a petroleum distillate are useful as solvents for certain oils and waxes.
It is to be understood that the various examples and proportions given are for the purpose of illustration, not limitation, of the invention and that many variations may be made therefrom without departing from the spirit of my invention.
I claim 1. A liquid fuel consisting of a petroleum distillate and a tertiary aliphatic alcohol.
2. A liquid fuel consisting of gasoline and tertiary butyl alcohol.
3. A motor fuel consisting of approximately 75 volumes of gasoline and 25 of tertiary butyl alcohol.
ROBERT H. VAN SCHAACK, J R.
They are good"
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US412568A US1907309A (en) | 1929-12-07 | 1929-12-07 | Liquid fuel |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US412568A US1907309A (en) | 1929-12-07 | 1929-12-07 | Liquid fuel |
Publications (1)
Publication Number | Publication Date |
---|---|
US1907309A true US1907309A (en) | 1933-05-02 |
Family
ID=23633520
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US412568A Expired - Lifetime US1907309A (en) | 1929-12-07 | 1929-12-07 | Liquid fuel |
Country Status (1)
Country | Link |
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US (1) | US1907309A (en) |
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2850368A (en) * | 1955-04-27 | 1958-09-02 | Exxon Research Engineering Co | Gasoline compositions |
US3250822A (en) * | 1963-01-17 | 1966-05-10 | Shell Oil Co | Hydration-alkylation process |
DE2444528A1 (en) * | 1973-09-18 | 1975-03-20 | Magyar Asvanyolaj Es Foeldgaz | FUEL FOR ENGINES WITH SPARK IGNITION AND ADDITIVES FOR THESE |
US3901664A (en) * | 1971-06-25 | 1975-08-26 | Chevron Res | Motor fuel |
US3988122A (en) * | 1971-06-25 | 1976-10-26 | Chevron Research Company | Motor fuel composition |
US4124485A (en) * | 1977-04-04 | 1978-11-07 | Gulf Research & Development Company | Separation of solids from coal liquids with an additive blend |
US4207077A (en) * | 1979-02-23 | 1980-06-10 | Texaco Inc. | Gasoline-ethanol fuel mixture solubilized with methyl-t-butyl-ether |
US4207076A (en) * | 1979-02-23 | 1980-06-10 | Texaco Inc. | Gasoline-ethanol fuel mixture solubilized with ethyl-t-butyl ether |
US4333739A (en) * | 1979-10-23 | 1982-06-08 | Neves Alan M | Blended ethanol fuel |
US4595784A (en) * | 1984-11-07 | 1986-06-17 | Board Of Control Of Michigan Technological University | Hydrocarbon fuel additives and method for preparing same |
US5681358A (en) * | 1995-09-29 | 1997-10-28 | Bloom & Kreten | Method of using an emergency fuel in an internal combustion engine |
WO1999020714A1 (en) * | 1997-10-22 | 1999-04-29 | Spare Tank, Llc | An emergency fuel for use in an internal combustion engine |
WO1999060076A1 (en) * | 1998-05-20 | 1999-11-25 | Bloom, Leonard | An emergency fuel for use in an internal combustion engine |
US6113660A (en) * | 1995-09-29 | 2000-09-05 | Leonard Bloom | Emergency fuel for use in an internal combustion engine and a method of packaging the fuel |
US6353143B1 (en) | 1998-11-13 | 2002-03-05 | Pennzoil-Quaker State Company | Fuel composition for gasoline powered vehicle and method |
US20040107634A1 (en) * | 2002-12-05 | 2004-06-10 | Greg Binions | Fuel compositions |
US20090277079A1 (en) * | 2008-05-08 | 2009-11-12 | Bp Corporation North America Inc. | Oxygenated gasoline composition having good driveability performance |
US20170067870A1 (en) * | 2015-09-08 | 2017-03-09 | Parker Hannifin Manufacturing Limited | Method |
-
1929
- 1929-12-07 US US412568A patent/US1907309A/en not_active Expired - Lifetime
Cited By (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2850368A (en) * | 1955-04-27 | 1958-09-02 | Exxon Research Engineering Co | Gasoline compositions |
US3250822A (en) * | 1963-01-17 | 1966-05-10 | Shell Oil Co | Hydration-alkylation process |
US3901664A (en) * | 1971-06-25 | 1975-08-26 | Chevron Res | Motor fuel |
US3988122A (en) * | 1971-06-25 | 1976-10-26 | Chevron Research Company | Motor fuel composition |
DE2444528A1 (en) * | 1973-09-18 | 1975-03-20 | Magyar Asvanyolaj Es Foeldgaz | FUEL FOR ENGINES WITH SPARK IGNITION AND ADDITIVES FOR THESE |
US4124485A (en) * | 1977-04-04 | 1978-11-07 | Gulf Research & Development Company | Separation of solids from coal liquids with an additive blend |
US4207077A (en) * | 1979-02-23 | 1980-06-10 | Texaco Inc. | Gasoline-ethanol fuel mixture solubilized with methyl-t-butyl-ether |
US4207076A (en) * | 1979-02-23 | 1980-06-10 | Texaco Inc. | Gasoline-ethanol fuel mixture solubilized with ethyl-t-butyl ether |
US4333739A (en) * | 1979-10-23 | 1982-06-08 | Neves Alan M | Blended ethanol fuel |
US4595784A (en) * | 1984-11-07 | 1986-06-17 | Board Of Control Of Michigan Technological University | Hydrocarbon fuel additives and method for preparing same |
US5681358A (en) * | 1995-09-29 | 1997-10-28 | Bloom & Kreten | Method of using an emergency fuel in an internal combustion engine |
US6110237A (en) * | 1995-09-29 | 2000-08-29 | Leonard Bloom | Emergency fuel for use in an internal combustion engine |
US6113660A (en) * | 1995-09-29 | 2000-09-05 | Leonard Bloom | Emergency fuel for use in an internal combustion engine and a method of packaging the fuel |
WO1999020714A1 (en) * | 1997-10-22 | 1999-04-29 | Spare Tank, Llc | An emergency fuel for use in an internal combustion engine |
WO1999060076A1 (en) * | 1998-05-20 | 1999-11-25 | Bloom, Leonard | An emergency fuel for use in an internal combustion engine |
US6353143B1 (en) | 1998-11-13 | 2002-03-05 | Pennzoil-Quaker State Company | Fuel composition for gasoline powered vehicle and method |
US20040107634A1 (en) * | 2002-12-05 | 2004-06-10 | Greg Binions | Fuel compositions |
US7410514B2 (en) * | 2002-12-05 | 2008-08-12 | Greg Binions | Liquid fuel composition having aliphatic organic non-hydrocarbon compounds, an aromatic hydrocarbon having an aromatic content of less than 15% by volume, an oxygenate, and water |
US20090277079A1 (en) * | 2008-05-08 | 2009-11-12 | Bp Corporation North America Inc. | Oxygenated gasoline composition having good driveability performance |
US8734543B2 (en) * | 2008-05-08 | 2014-05-27 | Butamax Advanced Biofuels Llc | Oxygenated gasoline composition having good driveability performance |
US9657244B2 (en) | 2008-05-08 | 2017-05-23 | Butamax Advanced Biofuels Llc | Oxygenated gasoline composition having good driveability performance |
US20170067870A1 (en) * | 2015-09-08 | 2017-03-09 | Parker Hannifin Manufacturing Limited | Method |
US9759706B2 (en) * | 2015-09-08 | 2017-09-12 | Parker Hannifin Manufacturing Limited | Method and kit for monitoring catalyst fines in heavy fuel oil |
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