US2046243A - Motor fuel - Google Patents
Motor fuel Download PDFInfo
- Publication number
- US2046243A US2046243A US648211A US64821132A US2046243A US 2046243 A US2046243 A US 2046243A US 648211 A US648211 A US 648211A US 64821132 A US64821132 A US 64821132A US 2046243 A US2046243 A US 2046243A
- Authority
- US
- United States
- Prior art keywords
- motor fuel
- ether
- gasoline
- octane number
- 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
- C10L1/02—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
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- 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 June' 30, 1936 UNTED STATES MOTOR FUEL Hyym E. Buc, Roselle, N. J assignor to Standard Oil. Development Company,
Delaware a corporation of No Drawing. Application December 21, 1932,
Serial N0. 648,211
11 Claims.
This invention relates to motor fuels and methods of preparing same for use in internal combustion engines and the like, and relates more particularly to motor fuels blended with agents which tend to reduce the knocking of the engine.-
Ethers have been added to motor fuels ,in the past and are generally known as knock inducers; but I have discovered that branched ethers, contrary to expectation, are particularly useful in reducing the knocking tendency of a hydrocarbon motor fuel such as the gasoline obtained from petroleum by known commercial methods. By the term branched ethers is meant an ether of the general formula RrQ- R where either one or both R and R are branched hydrocarbon radicals, either alike or unlike. If only one is branched, the other may be any other hydrocarbon radical, such as alkyl, aryl, etc. branched ethers which may be prepared in general from secondary and tertiary alcohols by any of the well known methods are, according to the invention, blended with a motor fuel in any desired proportion, such as 5%, 30%, 50% or more.
. As one particular example, 30% of isopropyl ether is added to a commercial gasoline motor fuel. Tests indicate that the octane number (the higher, the-octane number the less tendency to knock) at 375 F. was increased from 68.2 to 77.5, 30 resulting in an increase of 9.3.. 'This anti-knock agent has an additional advantage in that it has a high lead susceptibility, meaning that additions of lead tetraethyl will accomplish a stillfurther increase in octane number. For example, 1 c. c. of lead tetraethyl added to the commercial gasoline used in the above tests increased the octane number from 68.2 to 77.5 but adding 1 c. c. of lead tetraethyl to the blend of gasoline containing isopropyl ether'resulted in an octane number of 87.4, giving a lead susceptibilityof about 10. Some relatively good anti-knock agents have poor lead susceptibility.
The increase in octane number is roughly proportional to the amount of anti-knock agent used,
15%, a correspondingly less anti-knock effect will be produced.
Instead of using isopropyl ether, 9. number" of other branched others may be used; for example, a tertiary butyl ether or mixed others such as a methyl tertiary butyl ether or methyl tertiary amyl ether, etc.
In addition to the advantages mentioned above, the branched ethers contemplated by theinvention also possess the valuable characteristic that they may be blended in practically any proportion with hydrocarbon motor fuels and one need Such so if less than 30% isopropyl ether is used, say
not be concerned with the subject of water tolerance as they-are insoluble in water, the same as the hydrocarbon motor fuel. Alcohols are the best previously known blending agents, but they have the disadvantage of being dropped out 5 by slight additions of water.
Having thus described the invention, I do not desire to be limited by anyof the examples which have been given for the sake of illustration only but I desire to claim all novelty inherent in the 10 invention as far as the prior art permits.
I claim:
, l. A motor fuel comprising a mixture of hydrocarbons boiling within the gasoline range having its octane number improved by an addition 15 of a substantial amount of a normally liquid ether miscible with gasoline, and'boiling within the gasoline boiling range, and having the structure R-O-R' in which at least one of R and R is a branched aliphatic hydrocarbon radical and 20 both R and R are hydrocarbon groups.
2. A motor fuel according to the preceding claim in which at least one of R and R is an aliphatic hydrocarbon radical containing a tertiary carbon atom which is linked'to the ether oxygen.
3. A motor fuel according to claim 1 in which the ether constitutes at least, 5% ofthe composition. r
4. A motor fuel according to claim 1 in which the ether constitutes from 5 to of the com- 30 position.
5. A motor fuel according to claim 1 in which the octane number of the hydrocarbon mixture is further improved by the addition of an anti knock composition comprising a lead alkyl com- 5 pound.
6.1K motor fuel according to claim '1 in which the ether is isopropyl ether. '7. A motor fuel according to claim 1 in which the ether is isopropyl etheifland constitutes from 5 to 50% of .the fuel. v
8. A motor fuel comprising gasoline having its octane number improved by an addition of at least .5% of isopropyl ether.
value increased by admixture thereto of di-isopropyl ether in quantity ranging from about 10-30%.
10. A. motor fuel comprising a mixture of hydrocarbons boiling within the gasoline range having its octane number improved by anaddition of from 5 to 50% of methyl tertiary butyl ether. 0
11. A motor fuel comprising a mixture of hydrocarbons boiling within the gasoline range having its octane number improved by an addition of from 5 to 50% of methyl tertiary amyl ether.
. I-IYYM E. BUG.
9. A gasoline motor fuel having its anti-knock I
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US648211A US2046243A (en) | 1932-12-21 | 1932-12-21 | Motor fuel |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US648211A US2046243A (en) | 1932-12-21 | 1932-12-21 | Motor fuel |
Publications (1)
Publication Number | Publication Date |
---|---|
US2046243A true US2046243A (en) | 1936-06-30 |
Family
ID=24599862
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US648211A Expired - Lifetime US2046243A (en) | 1932-12-21 | 1932-12-21 | Motor fuel |
Country Status (1)
Country | Link |
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US (1) | US2046243A (en) |
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2668522A (en) * | 1951-11-29 | 1954-02-09 | Standard Oil Dev Co | Motor gasoline additive |
US3052528A (en) * | 1958-07-01 | 1962-09-04 | Shell Oil Co | Gasoline composition |
US3168385A (en) * | 1961-07-12 | 1965-02-02 | Socony Mobil Oil Co Inc | Motor fuels |
US3224848A (en) * | 1959-03-16 | 1965-12-21 | Shell Oil Co | Gasoline composition |
US3869262A (en) * | 1971-05-05 | 1975-03-04 | Oesterr Hiag Werke Ag | Fuel and additive for the production thereof |
EP0009966A1 (en) * | 1978-10-03 | 1980-04-16 | The Standard Oil Company | Motor fuel containing an anti-knock additive |
US4207076A (en) * | 1979-02-23 | 1980-06-10 | Texaco Inc. | Gasoline-ethanol fuel mixture solubilized with ethyl-t-butyl ether |
US4207077A (en) * | 1979-02-23 | 1980-06-10 | Texaco Inc. | Gasoline-ethanol fuel mixture solubilized with methyl-t-butyl-ether |
US4252541A (en) * | 1975-11-28 | 1981-02-24 | Texaco Inc. | Method for preparation of ethers |
EP0064253A2 (en) * | 1981-04-28 | 1982-11-10 | Veba Oel Ag | Gasoline |
US4407661A (en) * | 1981-12-07 | 1983-10-04 | Standard Oil Company | Motor fuel additives derived from shale oil |
US4723963A (en) * | 1984-12-18 | 1988-02-09 | Exxon Research And Engineering Company | Fuel having improved cetane |
US5078751A (en) * | 1990-04-04 | 1992-01-07 | Mobil Oil Corporation | Process for upgrading olefinic gasoline by etherification wherein asymmetrical dialkyl ethers are produced |
US5080691A (en) * | 1990-04-04 | 1992-01-14 | Mobil Oil Corp. | Process for the conversion of light olefins to ether-rich gasoline |
WO1993016150A1 (en) * | 1992-02-07 | 1993-08-19 | Nrg-Technologies, L.P. | Composition and method for producing a multiple boiling point ether gasoline component |
US6514299B1 (en) | 2000-11-09 | 2003-02-04 | Millennium Fuels Usa, Llc | Fuel additive and method therefor |
US20040060228A1 (en) * | 2002-09-30 | 2004-04-01 | Webber Kenneth M. | Gasoline additive and method of making same |
-
1932
- 1932-12-21 US US648211A patent/US2046243A/en not_active Expired - Lifetime
Cited By (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2668522A (en) * | 1951-11-29 | 1954-02-09 | Standard Oil Dev Co | Motor gasoline additive |
US3052528A (en) * | 1958-07-01 | 1962-09-04 | Shell Oil Co | Gasoline composition |
US3224848A (en) * | 1959-03-16 | 1965-12-21 | Shell Oil Co | Gasoline composition |
US3168385A (en) * | 1961-07-12 | 1965-02-02 | Socony Mobil Oil Co Inc | Motor fuels |
US3869262A (en) * | 1971-05-05 | 1975-03-04 | Oesterr Hiag Werke Ag | Fuel and additive for the production thereof |
US4252541A (en) * | 1975-11-28 | 1981-02-24 | Texaco Inc. | Method for preparation of ethers |
EP0009966A1 (en) * | 1978-10-03 | 1980-04-16 | The Standard Oil Company | Motor fuel containing an anti-knock additive |
US4412847A (en) * | 1978-10-03 | 1983-11-01 | The Standard Oil Company | Motor fuel additive |
US4207076A (en) * | 1979-02-23 | 1980-06-10 | Texaco Inc. | Gasoline-ethanol fuel mixture solubilized with ethyl-t-butyl ether |
US4207077A (en) * | 1979-02-23 | 1980-06-10 | Texaco Inc. | Gasoline-ethanol fuel mixture solubilized with methyl-t-butyl-ether |
EP0064253A3 (en) * | 1981-04-28 | 1984-09-19 | Veba Oel Ag | Carburettor fuel |
EP0064253A2 (en) * | 1981-04-28 | 1982-11-10 | Veba Oel Ag | Gasoline |
US4407661A (en) * | 1981-12-07 | 1983-10-04 | Standard Oil Company | Motor fuel additives derived from shale oil |
US4723963A (en) * | 1984-12-18 | 1988-02-09 | Exxon Research And Engineering Company | Fuel having improved cetane |
US5078751A (en) * | 1990-04-04 | 1992-01-07 | Mobil Oil Corporation | Process for upgrading olefinic gasoline by etherification wherein asymmetrical dialkyl ethers are produced |
US5080691A (en) * | 1990-04-04 | 1992-01-14 | Mobil Oil Corp. | Process for the conversion of light olefins to ether-rich gasoline |
WO1993016150A1 (en) * | 1992-02-07 | 1993-08-19 | Nrg-Technologies, L.P. | Composition and method for producing a multiple boiling point ether gasoline component |
US6017371A (en) * | 1992-02-07 | 2000-01-25 | Nrg Technologies, Inc. | Composition and method for producing a multiple boiling point ether gasoline component |
US6514299B1 (en) | 2000-11-09 | 2003-02-04 | Millennium Fuels Usa, Llc | Fuel additive and method therefor |
US20040060228A1 (en) * | 2002-09-30 | 2004-04-01 | Webber Kenneth M. | Gasoline additive and method of making same |
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