US1534573A - Fuel for internal-combustion engines - Google Patents
Fuel for internal-combustion engines Download PDFInfo
- Publication number
- US1534573A US1534573A US750657A US75065724A US1534573A US 1534573 A US1534573 A US 1534573A US 750657 A US750657 A US 750657A US 75065724 A US75065724 A US 75065724A US 1534573 A US1534573 A US 1534573A
- Authority
- US
- United States
- Prior art keywords
- boiling point
- ether
- fuel
- hydrocarbons
- combustion engines
- 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/185—Ethers; Acetals; Ketals; Aldehydes; Ketones
- C10L1/1852—Ethers; Acetals; Ketals; Orthoesters
-
- 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/19—Esters ester radical containing compounds; ester ethers; carbonic acid esters
-
- 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- 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
- C10L1/2222—(cyclo)aliphatic amines; polyamines (no macromolecular substituent 30C); quaternair ammonium compounds; carbamates
-
- 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- 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
- C10L1/2222—(cyclo)aliphatic amines; polyamines (no macromolecular substituent 30C); quaternair ammonium compounds; carbamates
- C10L1/2225—(cyclo)aliphatic amines; polyamines (no macromolecular substituent 30C); quaternair ammonium compounds; carbamates hydroxy containing
-
- 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- 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
-
- 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/24—Organic compounds containing sulfur, selenium and/or tellurium
-
- 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 OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- 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)
Definitions
- This invention relates to improvements in fuels ,for internal combustion engines, of the character disclosed in my application for Patent Serial No. 664586, filed September 24, 1923, of which the present applicati on is a continuation in part.
- an engine fuel including liquid hydrocarbons boiling above 160 (3., combined with an ether and a phenolic body.
- liquid hydrocarbons boiling above 160 C. may be utilized in low boiling point fuels, such as benzo-l, benzine or gasoline, providing the liquid hydrocarbons boiling above 160 C. are combined with an ether to promote the combustion or ignition of the mixture, and a phenolic body to retain the ether in the mixture.
- the primary object of the present inven tion is to improve fuels of this type by employing a body containing a phenyl radical,
- metallic phenyl compounds may be used but, of course, my invention is not limited to the use of these specific metallic phenyl compounds, as others may be used. While I prefer to use metallic phenyl compounds because they are more stable. my invention is not limited thereto. Other compounds containing the phenyl radical may be used in connection with the other ingredients of my fuel composition. For example, di-
- benzyl salicylate the benzyl amines, the benzyl anilines, the benzyl -alcohols and their derivatives may be used.
- the benzylhydroxy amines may also be used.
- Low boiling point hydrocarbons such as gasoline or benzol
- High boiling point hydrocarbons such as heavy gas oil
- 3O Ether A 1.5 Phenyl compound, forexample diphenyl telluride 0.5
- Low boiling point hydrocarbons 58
- High boiling point hydrocarbons (such as kerosene) 37 Ether.- 2.5
- Low boiling point hydrocarbons (including benzol) 30
- High boiling point hydrocarbons 40 Alcohol.- 27 Ether 1.5 Phenyl com ound, for example diphenyl te luride 1.5
- Low boiling'point hydrocarbons 30 High boiling point hydrocarbons (such as kerosene) 57 Ether 3 Phenyl compounds 10 5. Low boiling point hydrocarbons (such as gasoline or benzol) 68 High boiling point hydrocarbons (such as gas oil) 30 Ether 1.6 Dibenzyl diselenide .4
- An improved fuel for internal combustion engines including liquid hydrocarbons boiling above 160 C., and a smaller proportion of an ether and a compound containing a non-hydroxy phenyl radical.
- An improved fuel for internal combus boiling above 160 tion engines including a proportion of liquid hydrocarbons boiling above 16O. 0., a small proportion of ether'adapted to promote the combustion or ignition thereof, and a proportion of non-hydroxy phenyl compounds.
- An improved fuel for internal combustion engines including a considerable proportion of liquid hydrocarbons boiling above 160 C., a small proportion of an ether adapted to promote the combustion or ignition thereof, and a proportion ofmetallic phenyl compounds.
- An improved fuel for internal combustion engines includedin liquid hydrocarbons C5, and a smaller proportion-of an ether and radioactive metallic phenyl compounds.
- An improved fuel for internal combustion engines including aproportion of liquid hydrocarbons boiling above 160 0., a small,
- An improved fuel for internal combustion englnes including liquid hydrocarbons boiling above 160 (1, and a smaller proportion of an ether and a phenyl compound of a metal. 4
- An improved fuel for internal combustion engines including liquid hydrocarbons boiling above 160. (1, and a smaller proportion of an ether and a nonhydroxy phenyl compound.
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
'35 nadium, aluminum, etc.
Patented Apr. 21, 1925.
, UNITED. STATES PATENT OFFICE.
JEAN F. P. DE LA RIBOISIERE, OF WASHINGTON, DISTRICT OF COLUMBIA.
FUEL FOR INTERNAL-COMBUSTION ENGINES.
No Drawing.
To all whom it may concern:
Be it known that I, JEAN F. P. DE LA RIBOISIERE, a citizen of the French Republic, residing at Washington, D. C., U. S. A.,
have invented certain new and useful Improvements in Fuel for Internal-Combustion Engines, of whichthe following is a specification.
This invention relates to improvements in fuels ,for internal combustion engines, of the character disclosed in my application for Patent Serial No. 664586, filed September 24, 1923, of which the present applicati on is a continuation in part. In said application I have described an engine fuel including liquid hydrocarbons boiling above 160 (3., combined with an ether and a phenolic body. As stated in said application I have discovered that a large proportion of liquid hydrocarbons boiling above 160 C. may be utilized in low boiling point fuels, such as benzo-l, benzine or gasoline, providing the liquid hydrocarbons boiling above 160 C. are combined with an ether to promote the combustion or ignition of the mixture, and a phenolic body to retain the ether in the mixture.
The primary object of the present inven tion is to improve fuels of this type by employing a body containing a phenyl radical,
Among the compounds that I have found satisfactory are the phenyl compounds of selenium, tellurium, thorium, thallium, uranium, tungsten, titanium, bismuth, va-
These metallic phenyl compounds may be used but, of course, my invention is not limited to the use of these specific metallic phenyl compounds, as others may be used. While I prefer to use metallic phenyl compounds because they are more stable. my invention is not limited thereto. Other compounds containing the phenyl radical may be used in connection with the other ingredients of my fuel composition. For example, di-
benzyl salicylate, the benzyl amines, the benzyl anilines, the benzyl -alcohols and their derivatives may be used. The benzylhydroxy amines may also be used.
I have found from actual practice, that a mixture of this character will increase the speed of many types of motor vehicles at least 20 percent when climbing a steep hill. A demonstration in connection with a num- Application filed November 18., 1924. Serial No. 750,657.
ber of different types of motor cars shows an increase of speed in climbing a steep hill ot from 20 to 30 percent. As a matter of fact, in using fuel of this character, it has been demonstrated that the present mixture will increase the power of the motor at least 25 percent, and effect an economy in the consumption of fuel of about 30 percent over a similar demonstration with ordinary gasoline.
In practical use it has been found thatphenyl compounds, when radio active, have a very great influence on the power efficiency of the motor. 7
As examples of fuel mixtures which I have found to give very good results, I state as follows:
Per cent. 1. Low boiling point hydrocarbons (such as gasoline or benzol) 68 High boiling point hydrocarbons (such as heavy gas oil) 3O Ether A 1.5 Phenyl compound, forexample diphenyl telluride 0.5 2. Low boiling point hydrocarbons 58 High boiling point hydrocarbons (such as kerosene) 37 Ether.- 2.5 Phenyl compound, for example diphenyl telluride 2.5 3. Low boiling point hydrocarbons (including benzol) 30 High boiling point hydrocarbons 40 Alcohol.- 27 Ether 1.5 Phenyl com ound, for example diphenyl te luride 1.5
4. Low boiling'point hydrocarbons 30 High boiling point hydrocarbons (such as kerosene) 57 Ether 3 Phenyl compounds 10 5. Low boiling point hydrocarbons (such as gasoline or benzol) 68 High boiling point hydrocarbons (such as gas oil) 30 Ether 1.6 Dibenzyl diselenide .4
6. Low boiling point hydrocarbons 60 High boiling point hydrocarbons (such as kerosene) 37 Ether -4 2.5 Triphenyl of thallium 1 Per cent. 7. Low boiling point hydrocarbons 60 High boiling point hydrocarbons Low boiling point hydrocarbons- 60 High boiling point hydrocarbons (such as kerosene) 35.5 Ether .5 Tetra phenyl of vanadium, or other phenyl compounds of vanadium- 4 9. Low boiling point hydrocarbons 60 High boiling point hydrocarbons 15 such as kerosene)' 32 Et er 1 Dibenzyl salicylate 7 10. Low boiling point-hydrocarbons 60 High boiling point hydrocarbons (such as kerosene) 37.5 Ether .5 Benzyl aniline 2 11. Low boiling point hydrocarbons" 60 H'gh boiling point hydrocarbons 36.5 Ether .5
Benzyl hydroxylamine 3 While I have disclosed a few preferred examples, it is obvious that these proportions may be varied to suit conditions.
What I claim and desire to secure by Letters Patent is:
1. An improved fuel for internal combustion engines including liquid hydrocarbons boiling above 160 C., and a smaller proportion of an ether and a compound containing a non-hydroxy phenyl radical.
2. An improved fuel for internal combus boiling above 160 tion engines including a proportion of liquid hydrocarbons boiling above 16O. 0., a small proportion of ether'adapted to promote the combustion or ignition thereof, and a proportion of non-hydroxy phenyl compounds.
3. An improved fuel for internal combustion engines including a considerable proportion of liquid hydrocarbons boiling above 160 C., a small proportion of an ether adapted to promote the combustion or ignition thereof, and a proportion ofmetallic phenyl compounds.
An improved fuel for internal combustion engines includin liquid hydrocarbons C5, and a smaller proportion-of an ether and radioactive metallic phenyl compounds.
5. An improved fuel for internal combustion engines including aproportion of liquid hydrocarbons boiling above 160 0., a small,
proportion .of ether adapted to promote the combustion or ignition thereof, and a proportion of radioactive metallic phenyl compounds.
6. An improved fuel for internal combustion englnes including liquid hydrocarbons boiling above 160 (1, and a smaller proportion of an ether and a phenyl compound of a metal. 4
An improved fuel for internal combustion engines including liquid hydrocarbons boiling above 160. (1, and a smaller proportion of an ether and a nonhydroxy phenyl compound.
In testimony whereof I hereunto aflix my signature.
JEAN -F. P1 DE LA RIBOISIERE.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US750657A US1534573A (en) | 1924-11-18 | 1924-11-18 | Fuel for internal-combustion engines |
| GB29118/25A GB243357A (en) | 1924-11-18 | 1925-11-18 | Improvements in fuel for internal combustion engines |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US750657A US1534573A (en) | 1924-11-18 | 1924-11-18 | Fuel for internal-combustion engines |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1534573A true US1534573A (en) | 1925-04-21 |
Family
ID=25018726
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US750657A Expired - Lifetime US1534573A (en) | 1924-11-18 | 1924-11-18 | Fuel for internal-combustion engines |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US1534573A (en) |
| GB (1) | GB243357A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2994189A (en) * | 1954-01-04 | 1961-08-01 | Phillips Petroleum Co | Method of producing immediate thrust using fast burning fuels |
| US3082072A (en) * | 1959-12-03 | 1963-03-19 | George H Smith | Combustion promoter composition and methods of making and using same |
| US3130017A (en) * | 1952-07-05 | 1964-04-21 | Ethyl Corp | Antiknock fuel |
| US4479807A (en) * | 1981-01-09 | 1984-10-30 | Rebandt Ralph A | Gasoline-substitute fuel |
| 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 |
| US6353143B1 (en) | 1998-11-13 | 2002-03-05 | Pennzoil-Quaker State Company | Fuel composition for gasoline powered vehicle and method |
-
1924
- 1924-11-18 US US750657A patent/US1534573A/en not_active Expired - Lifetime
-
1925
- 1925-11-18 GB GB29118/25A patent/GB243357A/en not_active Expired
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3130017A (en) * | 1952-07-05 | 1964-04-21 | Ethyl Corp | Antiknock fuel |
| US2994189A (en) * | 1954-01-04 | 1961-08-01 | Phillips Petroleum Co | Method of producing immediate thrust using fast burning fuels |
| US3082072A (en) * | 1959-12-03 | 1963-03-19 | George H Smith | Combustion promoter composition and methods of making and using same |
| US4479807A (en) * | 1981-01-09 | 1984-10-30 | Rebandt Ralph A | Gasoline-substitute fuel |
| 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 |
| US6353143B1 (en) | 1998-11-13 | 2002-03-05 | Pennzoil-Quaker State Company | Fuel composition for gasoline powered vehicle and method |
Also Published As
| Publication number | Publication date |
|---|---|
| GB243357A (en) | 1926-11-25 |
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