US1683085A - Method of generating motive fluid - Google Patents
Method of generating motive fluid Download PDFInfo
- Publication number
- US1683085A US1683085A US447176A US44717621A US1683085A US 1683085 A US1683085 A US 1683085A US 447176 A US447176 A US 447176A US 44717621 A US44717621 A US 44717621A US 1683085 A US1683085 A US 1683085A
- Authority
- US
- United States
- Prior art keywords
- nitroglycerin
- explosive
- nitro
- camphor
- 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
- 238000000034 method Methods 0.000 title description 3
- 239000012530 fluid Substances 0.000 title description 2
- SNIOPGDIGTZGOP-UHFFFAOYSA-N Nitroglycerin Chemical compound [O-][N+](=O)OCC(O[N+]([O-])=O)CO[N+]([O-])=O SNIOPGDIGTZGOP-UHFFFAOYSA-N 0.000 description 22
- 239000000006 Nitroglycerin Substances 0.000 description 22
- 239000002360 explosive Substances 0.000 description 22
- 229960003711 glyceryl trinitrate Drugs 0.000 description 22
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 15
- 229930008380 camphor Natural products 0.000 description 15
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 14
- 238000002485 combustion reaction Methods 0.000 description 14
- 239000000446 fuel Substances 0.000 description 14
- 239000007788 liquid Substances 0.000 description 13
- 241000723346 Cinnamomum camphora Species 0.000 description 11
- 229960000846 camphor Drugs 0.000 description 11
- 239000000126 substance Substances 0.000 description 11
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 8
- 241000251729 Elasmobranchii Species 0.000 description 7
- 206010061218 Inflammation Diseases 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 230000004054 inflammatory process Effects 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 6
- 229910052721 tungsten Inorganic materials 0.000 description 6
- 239000010937 tungsten Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 230000008016 vaporization Effects 0.000 description 5
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 4
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 4
- 230000008014 freezing Effects 0.000 description 4
- 238000007710 freezing Methods 0.000 description 4
- 235000011187 glycerol Nutrition 0.000 description 4
- 150000002828 nitro derivatives Chemical class 0.000 description 4
- 238000009834 vaporization Methods 0.000 description 4
- VSOJWGJCPFPODA-UHFFFAOYSA-N 1,3-dinitropropane-1,2,3-triol Chemical compound [O-][N+](=O)C(O)C(O)C(O)[N+]([O-])=O VSOJWGJCPFPODA-UHFFFAOYSA-N 0.000 description 3
- SPSSULHKWOKEEL-UHFFFAOYSA-N 2,4,6-trinitrotoluene Chemical compound CC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O SPSSULHKWOKEEL-UHFFFAOYSA-N 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000000015 trinitrotoluene Substances 0.000 description 3
- IZUKQUVSCNEFMJ-UHFFFAOYSA-N 1,2-dinitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1[N+]([O-])=O IZUKQUVSCNEFMJ-UHFFFAOYSA-N 0.000 description 2
- -1 Furthermore Chemical compound 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000005474 detonation Methods 0.000 description 2
- 239000003721 gunpowder Substances 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000009877 rendering Methods 0.000 description 2
- 239000013535 sea water Substances 0.000 description 2
- XNKFCDGEFCOQOM-UHFFFAOYSA-N 1,2-dinitronaphthalene Chemical compound C1=CC=CC2=C([N+]([O-])=O)C([N+](=O)[O-])=CC=C21 XNKFCDGEFCOQOM-UHFFFAOYSA-N 0.000 description 1
- RJKGJBPXVHTNJL-UHFFFAOYSA-N 1-nitronaphthalene Chemical compound C1=CC=C2C([N+](=O)[O-])=CC=CC2=C1 RJKGJBPXVHTNJL-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- DSEKYWAQQVUQTP-UHFFFAOYSA-N Cerin Natural products CC12CCC3(C)C4CC(C)(C)CCC4(C)CCC3(C)C2CCC2(C)C1CC(O)C(=O)C2C DSEKYWAQQVUQTP-UHFFFAOYSA-N 0.000 description 1
- 239000004450 Cordite Substances 0.000 description 1
- 241001387976 Pera Species 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Natural products CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 235000015250 liver sausages Nutrition 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000001235 sensitizing effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B25/00—Compositions containing a nitrated organic compound
- C06B25/10—Compositions containing a nitrated organic compound the compound being nitroglycerine
- C06B25/12—Compositions containing a nitrated organic compound the compound being nitroglycerine with other nitrated organic compounds
Definitions
- the objectof the invention is mainly to provide a simpler, safer more efiiclent and convenient method of utilizing a self-combustive or explosive fuel for the generation.
- I preferably employ for a self-combustive and explosive liquid fuel, nitroglycerin de-sens it zed by dissolving in it a suitable de-sensitlzing substance orby forming a solutlon of another explosive substance in it, such as tr -n tromethyl-phenol, di-nitro-naphthalin, di-nitrobenzol, tri-nitro-toluene, or di-nitro-glycerin, or other suitable solid or llqilld explosive sub stance or substances, and may and sometimes do employ a solution in nitroglyce'rln of a suitable non-explosive combustible sub- ,stance to de-sensitize the nitroglycerin, such, 39 for example,'as gum camphor, wood alcohol,
- de-sensitizing agents further serve the purpose of materially lowering the freezing point of nitroglycerin.
- Y freezing point of'the nitroglycerin is thereby lowered below the freezing point of seawater, so that a torpedo containing such liquid fuel may remain immersed indefinitely, in seawater in winter, in any climate, without freezing of the nitroglycerin or the crystallization of any tion.
- I preferably employ such a proportion of de-sensitizing matter as shall render the nitroglycerin incapable of detonation under the conditions in which it may be employed in the combustion chamber of a torpedo-by the action of vaporization and inflammation for the generation ofheat for the produtcion of the necessary gases or vapors at the required t8mposure,
- Camphor has a very intense aflinity for nitrov glycerin, on account of the great solubility of camphor in nitroglycerin.
- the aifinity of camphor for nitroglycerin is such that but very little camphor will evaporate from a solution of nitroglycerin even after long exliquid nitrbglycerin fuel containing camphor being inadvertently spilled and exposed to the atmosphere, there will, after long exposure, remain in solution in the nitrogl erin the greater part of the camphor origina ly in solution, thereby effectually serving to prevent any quantity of the liquid for becoming sensitive and dangerous due to evaporation.
- wood alcohol and the like from the nitroglycerin, Furthermore, wood alcohol, acetone and the like, may be removed or washed out of the nitroglycerin with water, while it is very difficult to extract camphor fromnitroglycerin with water, the camphor being, for all practical purposes, as insoluble in water as is nitroglycerin.
- nitroglycerin another explosive substance less sensitive than nitroglycerin, such astri-nitro-methyl-phenol, or tri-nitro toluene, .di-nitro-naphthalin, di-nitro-benzol, or di-nitro-glycerin
- the nitroglycerin is de-sensitizectthereby, and the same purposes served as by the use of camphor, while the may evaporate leaving the camphor.
- I may and sometimes do em- 4 ploy both an explosive and a non-explosive substance or substances for the purpose of dedi-nitro-glycerln, or in sensitizing nitroglycerin, such, for example,
- I may employ, instead of addition to di-nitrog1 cerin, tri-nitro-toluene, di nitro-benzol or trl-nitro-methyl-phenol or other suitable explosive material.
- acetylene being an endo-thermic body, it is capable of generating heat from its decomposition or dissociation in the combustion chamber of the torpedo suflicientto render its own gases of decomposition incandescent without oxygen, so that by its use I am enabled to add to the -amount of heatgenerated, while at.
- the combustion chamber be made of tungsten or an alloy rich in tungsten, or a baflle or enflaming' plate of tungsten be employed upon which to play or jet the stream of liquid fuel into the combustion chamber, the high temperature of the tungsten rendering complete, efficient, constant and steady vaporization and inflammation off-the liquid fuel.
- the combustion chamber be made of tungsten or an alloy rich in tungsten, or a baflle or enflaming' plate of tungsten be employed upon which to play or jet the stream of liquid fuel into the combustion chamber, the high temperature of the tungsten rendering complete, efficient, constant and steady vaporization and inflammation off-the liquid fuel.
- the initial Va is preferably e ected either by the employment of a pilot flame of a portion of the material burned in a jet' of-air or by a pilot igniter made of an explosive material, such as .smokeles powder like cordite,
- the pilot flame or means of ignition maybe discontinued.
- the heat evolved or generated b the inflammation or combustion of the sel -combustive liquid will be suflicient to maintain at a very high temperature the bafile plate or vaporizing and enflaming plate against whichthe self-combustive fuel is pro ected or jetted in the combustion chamber of the torpedo.
- the heated walls of the chamber of the torpedo will serve the same urpose, the excess of heat in the products 0?
- combustion being absorbed by water admitted to the combustion chamber or into the stream of products of-combustion in their esca e from the combustion chamber, and by bem forced by the flame blast through a suita le mixingor atomizing device or means whereby the water is practically instantly evaporated by the absorption of heat from the stream of products of combustion and the steam superheated to any desired temperature, which temperature at present employed is about 1100 F. at the nozzle.
- a liquid explosive for driving torpedoes consisting of a nitro compound of glycerine holding in solution gum camphor, and a combustible non-explosive material.
- a liquid explosive for driving torpedoes consisting of holding in solution um camphor, acetylene a nitro compound of: glycerine gas, and a combusti le non-explosive mate- 3.
- a liquid explosive for driving torpedoes consisting of a nitro compound of glycerine holdingin solution gum camphor, acetylene gas, acetone and a combustible non-explosive material.
Landscapes
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Air Bags (AREA)
Description
Patented Sept. 4,. W28.
' mmson in l 'i OF HOPAQCONG BOROUGH, NEW JERSEY; LILIAN MAXIM. EXEOUTBIX OF SAID HUDSON MAXIM, DECEASED.
METHOD OF GENERATING MOTIVIE FLUID.
No Drawing.
The objectof the invention is mainly to provide a simpler, safer more efiiclent and convenient method of utilizing a self-combustive or explosive fuel for the generation.
of energy for the propulsion of torpedoes than has heretofore been employed.
In carrying out the invention, I preferably employ for a self-combustive and explosive liquid fuel, nitroglycerin de-sens it zed by dissolving in it a suitable de-sensitlzing substance orby forming a solutlon of another explosive substance in it, such as tr -n tromethyl-phenol, di-nitro-naphthalin, di-nitrobenzol, tri-nitro-toluene, or di-nitro-glycerin, or other suitable solid or llqilld explosive sub stance or substances, and may and sometimes do employ a solution in nitroglyce'rln of a suitable non-explosive combustible sub- ,stance to de-sensitize the nitroglycerin, such, 39 for example,'as gum camphor, wood alcohol,
acetone, mono-nitro-naphthalin or nitrobenzol, which latter two substances, although nitro compounds, still contain such a small percentage of combined oxygen as by themselves to be impractical or unsuitable as explosive compounds, either for the purpose of a self-combustive fuel for torpedoes or of a high explosive to reinforce the explosive blast of the warhead of the torpedo, as hereinafter described. r
All of the above de-sensitizing agents further serve the purpose of materially lowering the freezing point of nitroglycerin.
I have found that when a suflicientpercent- 5 age of a suitable dry-sensitizing substance or combination of substahces, such as those above enumerated, are employed effectuallyto de-sensitize the nitroglycerin and render it suitable as a liquid fuel for torpedoes, the
Y freezing point of'the nitroglycerin is thereby lowered below the freezing point of seawater, so that a torpedo containing such liquid fuel may remain immersed indefinitely, in seawater in winter, in any climate, without freezing of the nitroglycerin or the crystallization of any tion. x
I preferably employ such a proportion of de-sensitizing matter as shall render the nitroglycerin incapable of detonation under the conditions in which it may be employed in the combustion chamber of a torpedo-by the action of vaporization and inflammation for the generation ofheat for the produtcion of the necessary gases or vapors at the required t8mposure,
of the nitroglycerin out of solu-' torpedo,-but the employment centage of camiphor in addition to such an ex- Application filed February 23, 1922. Serial No. 447,176;
pera'ture to evaporate suflicient water to serve as an effective fuel; for driving torpedoes, as hereinafter described, and still, I preferably employ so small or limited .9, percentage of the de-sensitizing agent or substance or substances as shall renderany residual quantity of the fuel compound, in proximity to the warhead after a run of the torpedo, capable of being detonated by the detonation ofthe warhead of the torpedo, thereby permitting of the utilization of an residue of the self-combustive fuel to particle pate in and add to the force of the explosive blast of the warhead.
I have found'gum camphor to be a very efficient de-sensitizer of nitroglycerin.
Camphor has a very intense aflinity for nitrov glycerin, on account of the great solubility of camphor in nitroglycerin. The aifinity of camphor for nitroglycerin is such that but very little camphor will evaporate from a solution of nitroglycerin even after long exliquid nitrbglycerin fuel containing camphor being inadvertently spilled and exposed to the atmosphere, there will, after long exposure, remain in solution in the nitrogl erin the greater part of the camphor origina ly in solution, thereby effectually serving to prevent any quantity of the liquid for becoming sensitive and dangerous due to evaporation.
Other more volatile'solvents, such as acetone,
wood alcohol and the like, from the nitroglycerin, Furthermore, wood alcohol, acetone and the like, may be removed or washed out of the nitroglycerin with water, while it is very difficult to extract camphor fromnitroglycerin with water, the camphor being, for all practical purposes, as insoluble in water as is nitroglycerin. I have found, furthermore, that by dissolving in nitroglycerin another explosive substance less sensitive than nitroglycerin, such astri-nitro-methyl-phenol, or tri-nitro toluene, .di-nitro-naphthalin, di-nitro-benzol, or di-nitro-glycerin, the nitroglycerin is de-sensitizectthereby, and the same purposes served as by the use of camphor, while the may evaporate leaving the camphor.
so that in the event of someof the added explosive material, unlike a non--explosive combustible; is capable of.contributng heat to the reaction of self-combustion-of the liquid in the combustion chamber of the of a small perplosive adds to its solubility in nitroglycerin.
Therefore, I may and sometimes do em- 4 ploy both an explosive and a non-explosive substance or substances for the purpose of dedi-nitro-glycerln, or in sensitizing nitroglycerin, such, for example,
' as acetone or wood alcohol or both with dinitro-glycerin, or I may employ, instead of addition to di-nitrog1 cerin, tri-nitro-toluene, di nitro-benzol or trl-nitro-methyl-phenol or other suitable explosive material.
I some times employ a solution of acetylene gas in acetone dissolved in nitroglycerin, either with or without the addition of other de-sensitizing agents, the acetone serving the purpose of eflecting more rapid action of vaporization and inflammation of the liquid fuel in the combustion chamber of the toredo. Furthermore, acetylene being an endo-thermic body, it is capable of generating heat from its decomposition or dissociation in the combustion chamber of the torpedo suflicientto render its own gases of decomposition incandescent without oxygen, so that by its use I am enabled to add to the -amount of heatgenerated, while at. the; same time I lessen the roportion of oxygen in the products of com ustion, thereby rendering the gases of the products of combustion more reducing and less oxidizing than they otherwise would be, which is particularly advantageousif the combustion chamber be made of tungsten or an alloy rich in tungsten, or a baflle or enflaming' plate of tungsten be employed upon which to play or jet the stream of liquid fuel into the combustion chamber, the high temperature of the tungsten rendering complete, efficient, constant and steady vaporization and inflammation off-the liquid fuel. As tungsten at a high temperature is rapidly oxidized and destroyed in an oxidizing flame, the advantage ofa reducing flame is obvious when tungsten is employed for the purpose above specified.
i The initial Va is preferably e ected either by the employment of a pilot flame of a portion of the material burned in a jet' of-air or by a pilot igniter made of an explosive material, such as .smokeles powder like cordite,
rial.
orization and inflammation black gunpowder or of a combination of black gunpowder and smokeless powder, or of a rich in nitro glycerin.
After the initial vaporization and inflammation of the liquid fuel is efiected, the pilot flame or means of ignition maybe discontinued.
The heat evolved or generated b the inflammation or combustion of the sel -combustive liquid will be suflicient to maintain at a very high temperature the bafile plate or vaporizing and enflaming plate against whichthe self-combustive fuel is pro ected or jetted in the combustion chamber of the torpedo. In the absence of such baflle plate, the heated walls of the chamber of the torpedowill serve the same urpose, the excess of heat in the products 0? combustion being absorbed by water admitted to the combustion chamber or into the stream of products of-combustion in their esca e from the combustion chamber, and by bem forced by the flame blast through a suita le mixingor atomizing device or means whereby the water is practically instantly evaporated by the absorption of heat from the stream of products of combustion and the steam superheated to any desired temperature, which temperature at present employed is about 1100 F. at the nozzle.
What is claimed is I 1. A liquid explosive for driving torpedoes consisting of a nitro compound of glycerine holding in solution gum camphor, and a combustible non-explosive material. I 2. A liquid explosive for driving torpedoes consisting of holding in solution um camphor, acetylene a nitro compound of: glycerine gas, and a combusti le non-explosive mate- 3. A liquid explosive for driving torpedoes consisting of a nitro compound of glycerine holdingin solution gum camphor, acetylene gas, acetone and a combustible non-explosive material.
In testimony whereof I have signed my name to this specification.
' HUDSON MAXIM.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US447176A US1683085A (en) | 1921-02-23 | 1921-02-23 | Method of generating motive fluid |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US447176A US1683085A (en) | 1921-02-23 | 1921-02-23 | Method of generating motive fluid |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1683085A true US1683085A (en) | 1928-09-04 |
Family
ID=23775299
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US447176A Expired - Lifetime US1683085A (en) | 1921-02-23 | 1921-02-23 | Method of generating motive fluid |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1683085A (en) |
-
1921
- 1921-02-23 US US447176A patent/US1683085A/en not_active Expired - Lifetime
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN1321950C (en) | Dinitroamide-based liquid single-component propellant | |
| Natan et al. | Hypergolic ignition by fuel gellation and suspension of reactive or catalyst particles | |
| US2584803A (en) | Mono-fuel | |
| US2489051A (en) | Rocket propulsion utilizing hydrocarbon, sulfate turpentine, nitric acid, and sulfuric acid or oleum | |
| US2978864A (en) | Ammonium nitrate explosives | |
| RU2468240C1 (en) | Chamber of liquid-propellant rocket engine or gas generator with laser ignition device of fuel components, and its startup method | |
| US3773947A (en) | Process of generating nitrogen using metal azide | |
| US1683085A (en) | Method of generating motive fluid | |
| US2658874A (en) | Smoke agent | |
| US2986456A (en) | Liquid hydrocarbon fuel containing powdered coal, metal, and catalyst | |
| US3213609A (en) | High energy propellant and process employing hydrazines and nitro compounds | |
| US3252770A (en) | Lighter for charcoal and like material | |
| US1512354A (en) | Liquid composition for driving self-propelled torpedoes | |
| US3775199A (en) | Nitrogen generator | |
| US2774214A (en) | Rocket propulsion method | |
| US3383860A (en) | Low flame temperature gas generant containing ammonium iodate and methode of operatin a gas generator | |
| US20240150257A1 (en) | Monopropellant hydrogen peroxide fuel compositions suitable for use in no oxygen environments | |
| RU2439359C2 (en) | Method of creating jet thrust, liquid propellant rocket, and start-charge device to this end (versions) | |
| US3009316A (en) | Method of operating motors | |
| Chehroudi et al. | A novel distributed ignition method using single-wall carbon nanotubes (SWCNTs) and a low-power flash light | |
| US3151009A (en) | Catalyzed metal fuel | |
| WO2011001435A1 (en) | Hypergolic ignition system for gelled rocket propellant | |
| US4161104A (en) | Ignition of hydrazine-type monopropellants | |
| US1849051A (en) | Fuel oil for compression ignition engines | |
| US3113426A (en) | Cyclododecane as a high energy fuel |