US2398197A - Ketones in aviation gasoline - Google Patents
Ketones in aviation gasoline Download PDFInfo
- Publication number
- US2398197A US2398197A US476995A US47699543A US2398197A US 2398197 A US2398197 A US 2398197A US 476995 A US476995 A US 476995A US 47699543 A US47699543 A US 47699543A US 2398197 A US2398197 A US 2398197A
- Authority
- US
- United States
- Prior art keywords
- gasoline
- ketones
- ketone
- aviation gasoline
- aviation
- 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
- C10L10/00—Use of additives to fuels or fires for particular purposes
- C10L10/10—Use of additives to fuels or fires for particular purposes for improving the octane number
-
- 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
-
- 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
- C10L1/222—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
- C10L1/223—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond having at least one amino group bound to an aromatic carbon atom
Definitions
- This invention relates to new and useful motor fuels. More particularly it relates to aromaticamine-containing gasolines in which are incorporated minor amounts of certain ketones.
- the invention comprises an aviation gasoline containing minor amounts of aniline or an alkyl aniline plus minor amounts of a methyl propyl ketone or a methyl isobutyl ketone.
- Aromatic amines as anti-knock agents in gasoline has long been known. However, their employment in the place in which they are now most needed, high octane aviation gasoline, has met with various difilculties. Aromatic amines, as a class, are sparingly soluble in gasorline, particularly at relatively low temperature. This is especially true for aviation gasoline of low aromatic content. As a result, aromatic amines tend to separate from gasolines and this difliculty is greatly increased by the low temperatures at which modern airplanes are required to operate.
- alcohol in addition to the disadvantage ensuing from appreciable amounts of water contained in its commercially available form, has a relatively poor anti-knock value when used in a gasoline containing lead.
- ketones hitherto suggested,'none when present in small amount, satisfactorily prevents the abovedescribed difllculties when a gasoline is lowered to the temperature required for aviation fuel.
- the gasolines of the invention comprise predominantly light hydrocarbon distillates boiling within gasoline boiling range, and contain about 0.25%-10% of aniline or an alkyl derivative there-- of, plus a small amount of an asymmetrical aliphatic ketone having live or six carbon atoms.
- the total number of carbon atoms in the alkyl radicals of suitable alkyl anilines should not exceed 6, and the alkyl radical or radicals may be attached to the nitrogen atoms and/or to the Amounts between about 0.5% and 10% preferably 143%, are in general adequate to stabilize gasoline, containing the aromatic amines although larger or smaller quantities of ketone may be As a rule the amounts of the ketones should be suiiici'ent to prevent phase separation down to temperatures of at.
- gasoline may also contain up to about 6 cc. of commercial tetra-alkyl lead per gallon.
- aromatic amines which may be incorporated individually or together in a gasoline type motor fuel, mention may be made of the following: aniline, N-monoand di-methylaniline, corresponding ethyl and higher alkyl anilines (which may also be alkylated on the nucleus), toluidines, xylidines, mono-, di-, and tri-methyl and higher alkylated anilines (which may also be alkylated on the N atom), cumidines, pseudo cumidine, cymidine, etc.
- mix tures oi aromatic amines such as are produced by the nitration and reduction of a suitable aromatic petroleum fraction such as is described in U. S.
- Patents 1,844,362 and 2,252,099 may be emp y Since aniline (CtHsNHz) is the least gasolinesoluble of the aromatic amines'which possess a good anti-knock value, the invention will be illustrated with reference to aniline in aviation gasoline. Government specifications require that Separation Additive temperature , F. None. -20 l methy n-propylkctone -66 methy' n-propyl ketone -94 methy isobutyl ketone --83 Ingeneral, 3-1096 0! my ketones will adequately stabilize an aviation gasoline containing 0.254% anilinein the substantial absence of other aromatic constituents.
- a motor fuel consisting essentially o! a gasoline in which is dissolved .25 to 10% of a mononuclear aromatic amine having a total number of carbon atoms less than 7 in attached alwl radicals and between .5 and 5% of an asymmetric ketone selected from the group consisting of the five and six carbon atom di-alkyl ketones.
Description
Patented Apr. 9, 1946 2,398,191 KETONES IN AVIATION GASOLINE Albert L. Stanly, Berkeley, Calif assignor to Shell Development Company, San Francisco, Call!" a corporation of Delaware No Drawing. Application February 24, 1943, Serial No. 476,995
6 Claims.
This invention relates to new and useful motor fuels. More particularly it relates to aromaticamine-containing gasolines in which are incorporated minor amounts of certain ketones. In one of its preferred embodiments, the invention comprises an aviation gasoline containing minor amounts of aniline or an alkyl aniline plus minor amounts of a methyl propyl ketone or a methyl isobutyl ketone.
The use of aromatic amines as anti-knock agents in gasoline has long been known. However, their employment in the place in which they are now most needed, high octane aviation gasoline, has met with various difilculties. Aromatic amines, as a class, are sparingly soluble in gasorline, particularly at relatively low temperature. This is especially true for aviation gasoline of low aromatic content. As a result, aromatic amines tend to separate from gasolines and this difliculty is greatly increased by the low temperatures at which modern airplanes are required to operate.
It has been proposed to employ alcohols or leameleeular weight ketones as blending a ents to keep the aromatic amines in solution in the gasoline. However, these have proved unsatisfactory for. a number of reasons. The alcohols and lower ketones are very water soluble and tend not only to leave the gasoline and enter the water phase when water comes in contact with the gasoline (as-when gasoline is stored over water), but they also will take up significant amounts of water from the environment and incorporate it into the gasoline. The latter is par.- ticularly objectionable in an aviation fuel since the water may crystallize out of the gasoline and form ice in the carburetor when operating at high altitudes. Also alcohol, in addition to the disadvantage ensuing from appreciable amounts of water contained in its commercially available form, has a relatively poor anti-knock value when used in a gasoline containing lead. Of the ketones hitherto suggested,'none, when present in small amount, satisfactorily prevents the abovedescribed difllculties when a gasoline is lowered to the temperature required for aviation fuel.
Accordingly, it is an object of this invention to produce a gasoline containing a concentration of aromatic amines of appreciable anti-knock value, which gasoline remains stable at low temperatures. Another purpose is the production of an aviation gasoline containing an amount of aniline of substantial anti-knock value, which gasoline does not exhibit phase separation at low temperatures.
The gasolines of the invention comprise predominantly light hydrocarbon distillates boiling within gasoline boiling range, and contain about 0.25%-10% of aniline or an alkyl derivative there-- of, plus a small amount of an asymmetrical aliphatic ketone having live or six carbon atoms. The total number of carbon atoms in the alkyl radicals of suitable alkyl anilines should not exceed 6, and the alkyl radical or radicals may be attached to the nitrogen atoms and/or to the Amounts between about 0.5% and 10% preferably 143%, are in general adequate to stabilize gasoline, containing the aromatic amines although larger or smaller quantities of ketone may be As a rule the amounts of the ketones should be suiiici'ent to prevent phase separation down to temperatures of at. least -'l0 F. The minimum amount which will accomplish this varies considerably, depending not only on the amount of aromatic amines contained in.the gasoline, but also on the nature both of the particular amines and of the gasolines, as well as the presence of other ingredients which may act as mutual solvents. Such gasoline may also contain up to about 6 cc. of commercial tetra-alkyl lead per gallon.
Among the many aromatic amines which may be incorporated individually or together in a gasoline type motor fuel, mention may be made of the following: aniline, N-monoand di-methylaniline, corresponding ethyl and higher alkyl anilines (which may also be alkylated on the nucleus), toluidines, xylidines, mono-, di-, and tri-methyl and higher alkylated anilines (which may also be alkylated on the N atom), cumidines, pseudo cumidine, cymidine, etc. Similarly, mix tures oi aromatic amines such as are produced by the nitration and reduction of a suitable aromatic petroleum fraction such as is described in U. S. Patents 1,844,362 and 2,252,099, may be emp y Since aniline (CtHsNHz) is the least gasolinesoluble of the aromatic amines'which possess a good anti-knock value, the invention will be illustrated with reference to aniline in aviation gasoline. Government specifications require that Separation Additive temperature , F. None. -20 l methy n-propylkctone -66 methy' n-propyl ketone -94 methy isobutyl ketone --83 Ingeneral, 3-1096 0! my ketones will adequately stabilize an aviation gasoline containing 0.254% anilinein the substantial absence of other aromatic constituents.
Iclaim as my invention:
1. A motor fuel consisting essentially o! a gasoline in which is dissolved .25 to 10% of a mononuclear aromatic amine having a total number of carbon atoms less than 7 in attached alwl radicals and between .5 and 5% of an asymmetric ketone selected from the group consisting of the five and six carbon atom di-alkyl ketones.
2; The fuel of claim 1 in which the ketone contains one tertiary carbon atom.
3. The fuel of claim 1 in which the ketone is methyl n-propyl ketone.
4. .The fuel 0!, claim 1 in which the ketone is methyl isobutyl ketone.
5. The fuel of claim 1' in which the aromatic amine is xylidine.
6. An aviation gasoline containing about 0.25-1% aniline and between about 3 and 5% or an asymmetric ketone selected from the group consisting of the five and six carbon atom dialkyl ketones.
ALBEfitT L. BTANLY.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US476995A US2398197A (en) | 1943-02-24 | 1943-02-24 | Ketones in aviation gasoline |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US476995A US2398197A (en) | 1943-02-24 | 1943-02-24 | Ketones in aviation gasoline |
Publications (1)
Publication Number | Publication Date |
---|---|
US2398197A true US2398197A (en) | 1946-04-09 |
Family
ID=23894076
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US476995A Expired - Lifetime US2398197A (en) | 1943-02-24 | 1943-02-24 | Ketones in aviation gasoline |
Country Status (1)
Country | Link |
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US (1) | US2398197A (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2487909A (en) * | 1946-10-08 | 1949-11-15 | Eastman Kodak Co | Composition for use as antioxidant for motor fuels |
US4372753A (en) * | 1980-04-23 | 1983-02-08 | Source Technology, Inc. | Liquid fuel for use in internal combustion engines |
WO1994025545A1 (en) * | 1993-05-04 | 1994-11-10 | Exxon Research & Engineering Company | Unleaded aviation gasoline |
US20050229480A1 (en) * | 2004-04-15 | 2005-10-20 | Gaughan Roger G | Leaded aviation gasoline |
FR2894976A1 (en) * | 2005-12-16 | 2007-06-22 | Total France Sa | Composition of lead free aviation gasoline, comprises Avgas based fuel and two compounds e.g. of carboxylic acid esters and alcohols, carboxylic acid anhydrides and/or aromatic ethers and ketones |
US20110114536A1 (en) * | 2008-06-30 | 2011-05-19 | Total Raffinage Marketing | Aviation gasoline for aircraft piston engines, preparation process thereof |
US8628594B1 (en) | 2009-12-01 | 2014-01-14 | George W. Braly | High octane unleaded aviation fuel |
US10260016B2 (en) | 2009-12-01 | 2019-04-16 | George W. Braly | High octane unleaded aviation gasoline |
US10364399B2 (en) | 2017-08-28 | 2019-07-30 | General Aviation Modifications, Inc. | High octane unleaded aviation fuel |
US10377959B2 (en) | 2017-08-28 | 2019-08-13 | General Aviation Modifications, Inc. | High octane unleaded aviation fuel |
US10550347B2 (en) | 2009-12-01 | 2020-02-04 | General Aviation Modifications, Inc. | High octane unleaded aviation gasoline |
-
1943
- 1943-02-24 US US476995A patent/US2398197A/en not_active Expired - Lifetime
Cited By (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2487909A (en) * | 1946-10-08 | 1949-11-15 | Eastman Kodak Co | Composition for use as antioxidant for motor fuels |
US4372753A (en) * | 1980-04-23 | 1983-02-08 | Source Technology, Inc. | Liquid fuel for use in internal combustion engines |
WO1994025545A1 (en) * | 1993-05-04 | 1994-11-10 | Exxon Research & Engineering Company | Unleaded aviation gasoline |
US5470358A (en) * | 1993-05-04 | 1995-11-28 | Exxon Research & Engineering Co. | Unleaded aviation gasoline |
US20050229480A1 (en) * | 2004-04-15 | 2005-10-20 | Gaughan Roger G | Leaded aviation gasoline |
WO2005100513A2 (en) | 2004-04-15 | 2005-10-27 | Exxonmobil Research And Engineering Company | Improved leaded aviation gasoline |
US7862629B2 (en) | 2004-04-15 | 2011-01-04 | Exxonmobil Research And Engineering Company | Leaded aviation gasoline |
US20080244963A1 (en) * | 2005-12-16 | 2008-10-09 | Total France | Lead-Free Aviation Fuel |
WO2007074226A1 (en) * | 2005-12-16 | 2007-07-05 | Total France | Lead-free aviation fuel |
FR2894976A1 (en) * | 2005-12-16 | 2007-06-22 | Total France Sa | Composition of lead free aviation gasoline, comprises Avgas based fuel and two compounds e.g. of carboxylic acid esters and alcohols, carboxylic acid anhydrides and/or aromatic ethers and ketones |
US20110114536A1 (en) * | 2008-06-30 | 2011-05-19 | Total Raffinage Marketing | Aviation gasoline for aircraft piston engines, preparation process thereof |
US8741126B2 (en) | 2008-06-30 | 2014-06-03 | Total Marketing Services | Aviation gasoline for aircraft piston engines, preparation process thereof |
US8628594B1 (en) | 2009-12-01 | 2014-01-14 | George W. Braly | High octane unleaded aviation fuel |
US10260016B2 (en) | 2009-12-01 | 2019-04-16 | George W. Braly | High octane unleaded aviation gasoline |
US10550347B2 (en) | 2009-12-01 | 2020-02-04 | General Aviation Modifications, Inc. | High octane unleaded aviation gasoline |
US11098259B2 (en) | 2009-12-01 | 2021-08-24 | General Aviation Modifications, Inc. | High octane unleaded aviation gasoline |
US11674100B2 (en) | 2009-12-01 | 2023-06-13 | General Aviation Modifications, Inc. | High octane unleaded aviation gasoline |
US10364399B2 (en) | 2017-08-28 | 2019-07-30 | General Aviation Modifications, Inc. | High octane unleaded aviation fuel |
US10377959B2 (en) | 2017-08-28 | 2019-08-13 | General Aviation Modifications, Inc. | High octane unleaded aviation fuel |
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