US2813013A - Blends of acetylenic hydrocarbons - Google Patents
Blends of acetylenic hydrocarbons Download PDFInfo
- Publication number
- US2813013A US2813013A US586329A US58632956A US2813013A US 2813013 A US2813013 A US 2813013A US 586329 A US586329 A US 586329A US 58632956 A US58632956 A US 58632956A US 2813013 A US2813013 A US 2813013A
- Authority
- US
- United States
- Prior art keywords
- blends
- acetylenic hydrocarbons
- rating
- acetylenic
- blend
- 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
- 239000000203 mixture Substances 0.000 title description 11
- 229930195733 hydrocarbon Natural products 0.000 title description 9
- 150000002430 hydrocarbons Chemical class 0.000 title description 9
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- 238000010790 dilution Methods 0.000 description 6
- 239000012895 dilution Substances 0.000 description 6
- 239000000446 fuel Substances 0.000 description 6
- 230000035939 shock Effects 0.000 description 6
- FILUFGAZMJGNEN-UHFFFAOYSA-N pent-1-en-3-yne Chemical group CC#CC=C FILUFGAZMJGNEN-UHFFFAOYSA-N 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 238000007710 freezing Methods 0.000 description 3
- 230000008014 freezing Effects 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- JTJMJGYZQZDUJJ-UHFFFAOYSA-N phencyclidine Chemical compound C1CCCCN1C1(C=2C=CC=CC=2)CCCCC1 JTJMJGYZQZDUJJ-UHFFFAOYSA-N 0.000 description 2
- 239000002760 rocket fuel Substances 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- FQFCHEWSAJOUPA-UHFFFAOYSA-N 2,7-dimethylocta-1,7-dien-3,5-diyne Chemical compound CC(=C)C#CC#CC(C)=C FQFCHEWSAJOUPA-UHFFFAOYSA-N 0.000 description 1
- HXZCBIZQGFQJNX-UHFFFAOYSA-N 6-methylhepta-1,5-dien-3-yne Chemical group CC(C)=CC#CC=C HXZCBIZQGFQJNX-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000009863 impact test Methods 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B43/00—Compositions characterised by explosive or thermic constituents not provided for in groups C06B25/00 - C06B41/00
Definitions
- This invention relates to improvements in propellants, and more particularly pertains to improvements in acetylenic hydrocarbons for use as rocket fuels.
- the fuels that can be used for these purposes can be classified roughly into three categories. These three categories consist of the low performance type, the intermediate performance type, and the high performance type. Examples of the low performance type include the kerosene and refined petroleum fractions and the simple alcohols such as ethyl alcohol. These fuels are low in cost but they have relatively low specific impulse, or driving force, and they are not hypergolic; that is, they do not ignite spontaneously with the oxidizing agents with which they are employed commonly. At the other extreme, the jet fuels having very high specific impulse, such as diborane and the like, are very expensive, diflicult to produce, and are generally quite toxic.
- a principal object of this invention is to provide a blend of acetylenic hydrocarbons for use as rocket fuels.
- Another object is to provide such a blend having practical logistics, boiling and freezing points, vapor pressure, viscosity, density, specific impulse, heat of combustion, flame velocity, stability, ignition, corrosion and metal salts formation, and toxicity characteristics.
- acetylenic hydrocarbon having good ignition properties is dimethyl divinyl diacetylene, 2,7-dimethyl 1,7 octadiene 3,5-diyne, having the structural formula Tests of this compound indicated the high ignition rating of 8 with hexane dilution and 7 with benzene dilution.
- the compound has several undesirable characteristics. Its freezing point is 23 F., and it exhibits a high degree of instability towards mechanical and thermal shock. Its mechanical shock sensitivity is 80% on the drop weight impact test, one of the highest ratings of acetylenic hydrocarbons, and it bursts into flame when subjected to thermal shock.
- Methyl vinyl acetylene, Z-methyl l-butene 3-yne, having the structural formula has a very low freezing point, lower than l12 F., and a high heat of combustion, 19,680 B. t. u. per pound. It is also far more stable than dimethyl divinyl diacetylene, standing at 40% on the rating scale. Further, it is much cheaper to manufacture than the dimethyl divinyl diacetylene. Methyl vinyl acetylene is further characterized by an ignition rating of 5 with hexane or benzene dilution.
- This blend has an ignition rating of 7 with hexane dilution, and 6 with benzene dilution, an appreciable improvement over the 5 rating of methyl vinyl acetylene with both dilutions.
- the impact shock rating of the blend is substantially less than the rating of the dimethyl divinyl diacetylene.
- the blend described thus provides an acetylenic hydrocarbon rocket fuel having an ignition rating almost as good as that of the original dimethyl divinyl acetylene, as well as substantially improved shock resistance making feasible its use for the purposes intended.
- An acetylenic hydrocarbon rocket fuel consisting of a 30% mixture of dimethyl divinyl diacetylene in methyl vinyl acetylene.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
BLENDS OF ACETYLENIQ HYDROC f 1 No Drawing. Application May 21, 1956, Serial No. 586,329
1 Claim. c1. 52-5 This invention relates to improvements in propellants, and more particularly pertains to improvements in acetylenic hydrocarbons for use as rocket fuels.
It is well known that various jet propulsion devices including both monopropellant and bipropellant rocket systems and ram jets, have assumed great importance in recent times. The subject is of ever increasing importance in jet propulsion systems as used in airplanes, guided and unguided missiles, and jet-assisted takeoff units.
Generally, the fuels that can be used for these purposes can be classified roughly into three categories. These three categories consist of the low performance type, the intermediate performance type, and the high performance type. Examples of the low performance type include the kerosene and refined petroleum fractions and the simple alcohols such as ethyl alcohol. These fuels are low in cost but they have relatively low specific impulse, or driving force, and they are not hypergolic; that is, they do not ignite spontaneously with the oxidizing agents with which they are employed commonly. At the other extreme, the jet fuels having very high specific impulse, such as diborane and the like, are very expensive, diflicult to produce, and are generally quite toxic.
Although pure acetylenic hydrocarbons having prohibitively high melting points cannot be used as liquid fuels, by blending these high melting point materials with particular other acetylenic hydrocarbons of lower melting point, desirable blend characteristics can be obtained, thereby retaining a major portion of the advantageous features of both components. By suitably selecting the components and proportions of such blends, the stability characteristics of the blend to storage over prolonged periods of time and to elevated temperatures, as well as their shock sensitivity, can also be improved materially.
A principal object of this invention is to provide a blend of acetylenic hydrocarbons for use as rocket fuels.
Another object is to provide such a blend having practical logistics, boiling and freezing points, vapor pressure, viscosity, density, specific impulse, heat of combustion, flame velocity, stability, ignition, corrosion and metal salts formation, and toxicity characteristics.
Other objects and many of the attendant advantages of this invention will be readily appreciated as the same ice becomes better understood by reference to the following detailed description.
An acetylenic hydrocarbon having good ignition properties is dimethyl divinyl diacetylene, 2,7-dimethyl 1,7 octadiene 3,5-diyne, having the structural formula Tests of this compound indicated the high ignition rating of 8 with hexane dilution and 7 with benzene dilution. However, the compound has several undesirable characteristics. Its freezing point is 23 F., and it exhibits a high degree of instability towards mechanical and thermal shock. Its mechanical shock sensitivity is 80% on the drop weight impact test, one of the highest ratings of acetylenic hydrocarbons, and it bursts into flame when subjected to thermal shock.
Methyl vinyl acetylene, Z-methyl l-butene 3-yne, having the structural formula has a very low freezing point, lower than l12 F., and a high heat of combustion, 19,680 B. t. u. per pound. It is also far more stable than dimethyl divinyl diacetylene, standing at 40% on the rating scale. Further, it is much cheaper to manufacture than the dimethyl divinyl diacetylene. Methyl vinyl acetylene is further characterized by an ignition rating of 5 with hexane or benzene dilution.
A 30% mixture of dimethyl divinyl diacetylene in methyl vinyl acetylene remained liquid at 40 F. This blend has an ignition rating of 7 with hexane dilution, and 6 with benzene dilution, an appreciable improvement over the 5 rating of methyl vinyl acetylene with both dilutions. The impact shock rating of the blend is substantially less than the rating of the dimethyl divinyl diacetylene.
The blend described thus provides an acetylenic hydrocarbon rocket fuel having an ignition rating almost as good as that of the original dimethyl divinyl acetylene, as well as substantially improved shock resistance making feasible its use for the purposes intended.
Obviously many modifications and variations of the present invention are possible in the light of the above teachings. It is therefore to be understood that within the scope of the appended claim the invention may be practiced otherwise than as specifically described.
We claim:
An acetylenic hydrocarbon rocket fuel consisting of a 30% mixture of dimethyl divinyl diacetylene in methyl vinyl acetylene.
References Cited in the file of this patent UNITED STATES PATENTS 2,573,471 Malina et al Oct. 30, 1951 2,702,984 Britton et al Mar. 1, 1955
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US586329A US2813013A (en) | 1956-05-21 | 1956-05-21 | Blends of acetylenic hydrocarbons |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US586329A US2813013A (en) | 1956-05-21 | 1956-05-21 | Blends of acetylenic hydrocarbons |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2813013A true US2813013A (en) | 1957-11-12 |
Family
ID=24345292
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US586329A Expired - Lifetime US2813013A (en) | 1956-05-21 | 1956-05-21 | Blends of acetylenic hydrocarbons |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2813013A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3086356A (en) * | 1959-05-18 | 1963-04-23 | Air Reduction | Hypergolic fuel-oxidizer system |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2573471A (en) * | 1943-05-08 | 1951-10-30 | Aerojet Engineering Corp | Reaction motor operable by liquid propellants and method of operating it |
| US2702984A (en) * | 1950-07-25 | 1955-03-01 | Phillips Petroleum Co | Method and fuel for operating jet engines |
-
1956
- 1956-05-21 US US586329A patent/US2813013A/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2573471A (en) * | 1943-05-08 | 1951-10-30 | Aerojet Engineering Corp | Reaction motor operable by liquid propellants and method of operating it |
| US2702984A (en) * | 1950-07-25 | 1955-03-01 | Phillips Petroleum Co | Method and fuel for operating jet engines |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3086356A (en) * | 1959-05-18 | 1963-04-23 | Air Reduction | Hypergolic fuel-oxidizer system |
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