US2993768A - Liquid monofuel and method of forming - Google Patents
Liquid monofuel and method of forming Download PDFInfo
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- US2993768A US2993768A US536054A US53605455A US2993768A US 2993768 A US2993768 A US 2993768A US 536054 A US536054 A US 536054A US 53605455 A US53605455 A US 53605455A US 2993768 A US2993768 A US 2993768A
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- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06D—MEANS FOR GENERATING SMOKE OR MIST; GAS-ATTACK COMPOSITIONS; GENERATION OF GAS FOR BLASTING OR PROPULSION (CHEMICAL PART)
- C06D5/00—Generation of pressure gas, e.g. for blasting cartridges, starting cartridges, rockets
- C06D5/08—Generation of pressure gas, e.g. for blasting cartridges, starting cartridges, rockets by reaction of two or more liquids
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- 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 a liquid monofuel and particularly to a'liqu'id monopropellant for use in reaction chambers or combustors of rocket and jet engines to provide hot gases having predictable characteristics.
- the invention further relates to a method of adjusting the decomposition and storage characteristics of. a liquid monofuel.
- alkylene Oxides such as ethylene oxide
- mo'nopropellants since these substances are inflammable and explosive and have other desirable properties.
- alkylene oxides such as ethylene oxide
- theautoignition temperature and vapor pressure of alkylene oxides, such as ethylene oxide and propylene oxide are greater than is necessary or practical for combustor operation and the storage density is so low that, for example, only an inadequate amount of fuel may be carried in aircraft in which a particular combustor is employed.
- the low storage density of alkylene oxides, such as ethylene 'oxide is a particular disadvantage of these fuels because the problem of increasing the range of jet and rocket operated aircraft is of great significance.
- Theprincipal object of the present invention is to provide a liquid monofuel solution, characterized by a selected decomposition temperature and freezing point, and a low autoignition temperature and vapor pressure, and a high storage density.
- Another object of the invention is to provide a liquid monofuel having a relatively low autoignition temperature and vapor pressure and which also has a selected freezing point and a relatively. high shock stability and storage density, making possible an increased range in aircraft in which the monofuel is used.
- Another object of the invention is to provide a method of adjusting the decomposition temperature, autoignition temperature and storage density of a liquid monofuel.
- the inadequacies of an alkylene oxide as a liquid monofuel are largely overcome by the combination of one or more alkylene oxides (or alkyl nitrates which may be substituted for alkylene oxides) with one or more alkylene carbonates and one or more nitroalkanes.
- Alkylene carbonates and nitroalkanes have in common the efiect of reducing the autoignition temperature and vapor pressure of alkylene oxide either alone or in combination with alkyl nitrate or of alkyl nitrate alone, and of increasing the storage density thereof, so that the addition of alkylene carbonate and nitroalkane to alkylene oxide improves the decomposition and storage characteristics of a liquid monofuel.
- the use of both alkylene carbonate and nitroalkane, in addition to'alkylene oxide (or alkyl nitrate) provides a liquid monofuel having a predictable and adjustable decomposition temperature, storage density and power output.
- the decomposition temperature of the liquid monofuel is relatively low.
- the decomposition temperature is substantially increased. In either case, however, the auto-v ignition temperature and vapor pressure of the resultant solution are rendered relatively low and the storage density of the solution is made relatively high.
- theterm decomposition tempera ture means the same as what is frequently referred to as the total temperature which is the maximum fiame' temperature in thereaction chamber or combustor.
- a preferred liquid monofuel is characterized by a decom: position or total temperature below 2200 F., since higher temperatures are unsuitable for gas turbine engines and require special cooling systems for rocket engines.
- the minimum decomposition temperature which is useful in a liquid monofuel is about 1200 F. Such a temperature is suitable for a gas producer used for tank pressurization.
- a preferred decomposition temperature for a liquid monofuel is about 1800 F., and this is the approximate decomposition temperature of ethylene oxide used alone. However, as indicated above, it is undesirable to use ethylene oxide alone, since the autoignition temperature and vapor pressure are high, and the storage density is low. It is desirable to keep vapor pressure at a minimum in order to permit the use of relatively lightweight fuel tanks, instead of strong and heavy ones.
- the present invention contemplates adding an alkylene carbonate, such as ethylene carbonate, and a nitroalkane, such as nitromethane, in approximately equal parts by weight relative to each other, to a major portion of an alkylene oxide, such as ethylene oxide, which may also include some alkyl nitrate, such as npropyl nitrate.
- an alkylene carbonate such as ethylene carbonate
- a nitroalkane such as nitromethane
- ethylene oxide which may also include some alkyl nitrate, such as npropyl nitrate.
- a solution containing equal parts of ethylene carbonate and nitromethane with ethylene oxide for example, has approximately the same decomposition temperature as ethylene oxide alone.
- the combination liquid monofuel solution has the desired decomposition temperature but is greatly improved relative to such factors as autoignition, vapor pressure and storage density.
- Ethylene oxide for example, is characterized by a freezing point lower than that of ethylene carbonate, for example, or nitromethane, for example, and its use in substantial proportion is necessary to keep the resulting freezing point of the mixture below approximately 65 F. If the freezing point of the fuel were above this tem perature the fuel would tend to freeze up in certain situations, particularly in high altitude use, which woud be a considerable disadvantage.
- alkylene oxides and ethylene oxide in particular, have a relatively high stability or shock insensitivity, and are relatively difficult to explode. Therefore, when alkyl nitrates, such as n-propyl nitrate, are substituted for them, this substitution is ordinarily only partial.
- Nitromethane and ethylene carbonate as examples of nitroalkanes and alkylene oxides respectively, however, are relatively easy to explode and difficult to handle. It follows that substantial proportions of ethylene oxide or its equivalent should be employed so that the resulting fuel will be safe to handle. For example, preferable ranges in this liquid monofuel composition are by weight: 4080% ethylene oxide, 530% nitramethane, and 5-30% ethylene carbonate.
- alkylene oxide such as ethylene oxide
- alkylene carbonate such as ethylene carbonate
- Nitroalkanes may also be used in the liquid monofuel of this invention. They may be used as mixtures or as an individual species such as nitromethane, nitroethane,-a nitropropane or a nitrobutane.
- the combination witha major proportion of an alkylene oxide of substantially equal proportions by weight of nitroalkane and alkylene carbonate constitutes the preferred form of the invention. They may also be entirely omitted from the fuel composition.
- Example 1 A specific preferred example of a liquid monofuel having a decomposition temperature of approximately 1800' F. and a freezing point of approximately 65 F., comprising 2 5% ethylene carbonate, 25% nitromethaneand
- Example 2 A specific example of a solution having a freezing point of approximately 100 F. and a decomposition temperature of approximately 1800 F., is 10% ethylene carbonand a nitroalkane such as nitromethane, forms a true solution which is miscible in'all proportions of the three elements, as is essential for a satisfactory liquid monopropellant. Because of this complete miscibility, the considerations taken into account when the fuel is prepared are the properties which it is desired to attain, and particularly the exact decomposition temperature required.
- a major proportion of the fuel comprises one or more alkylene oxides.
- Such oxides may, for example, be selected from the group comprising ethylene oxide, propylene oxide, 1,3 butadiene dioxide and related diene and triene oxides and dioxides of the lower order olefins and parafiins.
- alkyl nitrates may be substituted for a portion of the alkylene oxides.
- these compounds are methyl nitrate, ethyl nitrate, n-propyl nitrate, isopropyl nitrate and various butyl nitrates such as n-butyl nitrate.
- the simple binary combination of an alkylene oxide, such as ethylene oxide, with an alkyl nitrate, such as n-propyl nitrate will form a satisfactory liquid monofuel.
- the binary composition can comprise fifty percent of each.
- alkylene oxide is used in combination with the other fuel components of this invention even when it is largely replaced by alkyl nitrate, since the alkylene oxides reduce the danger of explosions in handling.
- alkyl nitrate may be used as a fuel component as well as afsingle species.
- Alkylene carbonates may also be used in the liquid monofuel of this invention. They may be used as mixate, 10% nitromethane and ethylene oxide, all proportions being by weight.
- Example 3 A decomposition temperature of approximately 2200 F. is obtained with a liquid monofuel comprising 20% by weight of nitromethane, 5% by weight ethylene canbonate and 75% by weight ethylene oxide. Although a fuel decomposition temperature of about l800 F. is preferred for flight of substantial duration, a decomposition temperature may rise as high as about 2200 F. for short flights. For such situations it is merely necessary to increase the nitromethane content relative to the ethylene carbonate by amounts such that the desired decomposition temperature will be achieved.
- Example 4 It may be desirable to lower the decomposition temperature of a liquid monofuel to approximately 1200 F. when a fuel is used to run a gas producer for tank pressurization. To achieve such a temperature it'is necessary to increase the proportion of ethylene carbonate relative to nitromethane.
- a 1200 F. decomposition solution may be achieved by employing 5% nitromethane, 25% ethylene carbonate and 70% ethylene oxide in proportion by weight.
- the principle of the invention relates to the method of varying the decomposition temperature of a solution by varying the proportions of its components such as alkylene carbonate and nitroalkane relative to one another.
- the resulting solution has improved characteristics relative to autoignition, storage density and vapor pressure.
- a second principle of the invention relates to the method of varying the proportion of alkylene oxide in a liquid monofuel to change the freezing point of the resulting solution, the main consideration being to employ as little alkylene oxide as possible and yet achieve a sufliciently low freezing point.
- a fuel composition mixture consisting essentially of a major proportion by weight of at least one component selected from the group consisting of lower alkylene oxides and lower alkyl nitrates and a minor proportion by weight of at least one component selected from the group consisting of lower alkylene carbonates and lower nitro alkanes.
- a fuel composition consisting essentially of a major proportion by weight of at least one lower alkylene oxide and at least one lower alkyl nitrate and a minor proportion by weight of at least one lower alkylene carbonate and at least one lower nitroalkane.
- a fuel composition consisting essentially of a major proportion by weight of at least one lower alkylene oxide and a minor proportion by weight of at least one lower alkylene carbonate and at least one lower nitroalkane.
- a fuel composition consisting essentially of a major proportion by weight of at least one lower alkylene oxide and a minor proportion by weight of at least one lower alkylene carbonate.
- a fuel composition consisting essentially of a major proportion by weight of at least one lower alkylene oxide and a minor proportion by weight of at least one lower nitroalkane.
- a fuel composition consisting essentially of a major proportion by weight of at least one lower alkyl nitrate and a minor proportion by weight of at least one lower alkylene carbonate and at least one lower nitroalkane.
- a fuel composition consisting essentially of a major proportion by weight of at least one lower alkyl nitrate and a minor proportion by weight of at least one lower alkylene carbonate.
- a fuel composition consisting essentially of a major proportion by weight of at least one lower alkyl nitrate and a minor proportion by weight of at least one lower nitroalkane.
- a fuel composition consisting essentially of a major proportion by weight of ethylene oxide and a minor proportion by weight of nitromethane.
- a fuel composition consisting essentially of a major proportion by weight of propylene oxide and a minor proportion by weight of nitromethane.
- a liquid monopropellant for use in combustors 6 consisting essentially of a major proportion by weight of ethylene oxide, and a minor proportion by weight of ethylene carbonate and nitromethane.
- a liquid monopropellant for use in jet and rocket combustors consisting essentially of a major proportion by weight of ethylene oxide and a minor proportion by weight of both ethylene carbonate and nitromethane, the proportions of the ethylene carbonate and nitromethane relative to each other being selected to achieve the decomposition temperature required for the combustor in which the monopropellant is to be employed.
- a liquid monopropellant for use as a rocket and gas turbine fuel consisting essentially of a major proportion of ethylene oxide, the balance being ethylene carbonate :and nitromethane in substantially equal proportions by weight.
- a gas turbine and rocket fuel consisting essentially of the following ingredients and proportions by weight: ethylene oxide, 25% nitromethane, 25% ethylene carbonate.
- a gas turbine and rocket fuel consisting essentially of the following ingredients and proportions by weight: 80% ethylene oxide, 10% nitromethane, 10% ethylene carbonate.
- a gas turbine and rocket fuel consisting essentially of the following ingredients and proportions by weight: ethylene oxide, 20% nitromethane and 5% ethylene carbonate.
- a rocket and gas turbine fuel consisting essentially of the following ingredients in proportions by weight: 70% ethylene oxide, 5% nitromethane, 25% ethylene carbonate.
- a liquid monopropellant consisting essentially of the following ingredients in proportions by weight: 40- ethylene oxide, 530% nitromethane and 5-30% ethylene carbonate.
- a liquid monopropellant consisting essentially of the following ingredients in the following proportions by weight: 5080% ethylene oxide, 1025% nitromethane and 10-25% ethylene carbonate, the proportion of nitromethane being substantially equal to the proportion of ethylene carbonate,
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Description
LIQUID MONOFUEL AND IVEETHOD' or FORMING Robert A. Holzl, Glendale, Califi, assignor, by mesne assignments, to Sundstrand Corporation, a corporation of Illinois No Drawing. Filed Sept. 22,1955, Ser. No. 536,054 19'Claims. (Cl. 52-
This application is a continuation in part of, copending application, Serial No. 447,421 filed August-2, 1954, now abandoned which is a continuation in part of Serial No. 353,240 filed May 5, 1953, now abandoned.
This invention-relates to a liquid monofuel and particularly to a'liqu'id monopropellant for use in reaction chambers or combustors of rocket and jet engines to provide hot gases having predictable characteristics. The invention further relates to a method of adjusting the decomposition and storage characteristics of. a liquid monofuel.
In the field of propellants for use in reaction chambers or combustors of rocket and jet engines, alkylene Oxides, such as ethylene oxide, havebeen proposed for use as mo'nopropellants, since these substances are inflammable and explosive and have other desirable properties. There are some types of-combustors in which alkylene oxides, such as ethylene oxide, alone areunsuitable because of a decomposition temperature which is either too low or too high. Moreover, theautoignition temperature and vapor pressure of alkylene oxides, such as ethylene oxide and propylene oxide, are greater than is necessary or practical for combustor operation and the storage density is so low that, for example, only an inadequate amount of fuel may be carried in aircraft in which a particular combustor is employed. The low storage density of alkylene oxides, such as ethylene 'oxide, is a particular disadvantage of these fuels because the problem of increasing the range of jet and rocket operated aircraft is of great significance.
Theprincipal object of the present invention is to provide a liquid monofuel solution, characterized by a selected decomposition temperature and freezing point, and a low autoignition temperature and vapor pressure, and a high storage density. v I
Another object of the invention is to provide a liquid monofuel having a relatively low autoignition temperature and vapor pressure and which also has a selected freezing point and a relatively. high shock stability and storage density, making possible an increased range in aircraft in which the monofuel is used.
Another object of the invention is to provide a method of adjusting the decomposition temperature, autoignition temperature and storage density of a liquid monofuel.
These and other objects of the invention are elaborated and become more apparent in the following description.
According to the present invention, the inadequacies of an alkylene oxide as a liquid monofuelare largely overcome by the combination of one or more alkylene oxides (or alkyl nitrates which may be substituted for alkylene oxides) with one or more alkylene carbonates and one or more nitroalkanes. Alkylene carbonates and nitroalkanes have in common the efiect of reducing the autoignition temperature and vapor pressure of alkylene oxide either alone or in combination with alkyl nitrate or of alkyl nitrate alone, and of increasing the storage density thereof, so that the addition of alkylene carbonate and nitroalkane to alkylene oxide improves the decomposition and storage characteristics of a liquid monofuel. Moreover, the use of both alkylene carbonate and nitroalkane, in addition to'alkylene oxide (or alkyl nitrate) provides a liquid monofuel having a predictable and adjustable decomposition temperature, storage density and power output.
Pat ented July 25, 1961 However, it has been discovered that by adding an alkylene carbonate to an alkylene oxide or alkyl nitrate it is possible to reduce the decomposition temperature of the resultant mixture, and that by adding a nitroalkane to an alkylene oxide or alkyl nitrate composition it is possible to increase the decomposition temperature thereof. Furthermore, alkyl nitrates can be substituted in whole or in part for alkylene oxides in such compositions.
Complete substitution, however, raises the threshold of physical shock stability and it is preferred to keep at least some alkylene oxide in all fuel compositions for safe handling. Accordingly, by varying the percentages of alkylene carbonate and nitroalkane with relation to each other it is possible to achieve a liquid monofuel having the precise decomposition characteristics required for combustors in which such a fuel is used.
Where the amount of alkylene carbonate is relatively large in comparison with the amount of nitroalkane, the decomposition temperature of the liquid monofuel is relatively low. On the other hand, where the amount of nitroalkane is large in comparison with the amount of alkylene carbonate, the decomposition temperature is substantially increased. In either case, however, the auto-v ignition temperature and vapor pressure of the resultant solution are rendered relatively low and the storage density of the solution is made relatively high.
In view of the above, it is clear that the exact proportions of the elements in the liquid monofuel will vary in different applications depending upon the exact characteristics which it is desired to attain for the combustor in which the fuel is to be used. Indeed, it is not always necessary to use both of, these ingredients and in some fuel compositions only one of them is used.
As here employed, theterm decomposition tempera ture, means the same as what is frequently referred to as the total temperature which is the maximum fiame' temperature in thereaction chamber or combustor. A preferred liquid monofuel is characterized by a decom: position or total temperature below 2200 F., since higher temperatures are unsuitable for gas turbine engines and require special cooling systems for rocket engines. On the other hand, the minimum decomposition temperature which is useful in a liquid monofuel is about 1200 F. Such a temperature is suitable for a gas producer used for tank pressurization.
The combination of a nitroalkane and an alkylene oxide alone, (which may or may not also include an alkyl nitrate) without the addition of an alkylene carbonate results in acceptable performance for some situa tions, but is usually characterized by excessively high decomposition temperatures which may be of the order of 3500 F. Hence, special cooling equipment is necessary for rocket use and the fuel is usually unsuitable for gas turbine use.
A preferred decomposition temperature for a liquid monofuel is about 1800 F., and this is the approximate decomposition temperature of ethylene oxide used alone. However, as indicated above, it is undesirable to use ethylene oxide alone, since the autoignition temperature and vapor pressure are high, and the storage density is low. It is desirable to keep vapor pressure at a minimum in order to permit the use of relatively lightweight fuel tanks, instead of strong and heavy ones.
In a preferred form, the present invention contemplates adding an alkylene carbonate, such as ethylene carbonate, and a nitroalkane, such as nitromethane, in approximately equal parts by weight relative to each other, to a major portion of an alkylene oxide, such as ethylene oxide, which may also include some alkyl nitrate, such as npropyl nitrate. Since nitromethane, for example, has the effect of raising the decomposition temperature, and ethylene carbonate, for example, has the effect of. lowenng the decomposition temperature, in about the same proportion, a solution containing equal parts of ethylene carbonate and nitromethane with ethylene oxide, for example, has approximately the same decomposition temperature as ethylene oxide alone. The combination liquid monofuel solution has the desired decomposition temperature but is greatly improved relative to such factors as autoignition, vapor pressure and storage density.
There is a practical minimum relative amount of alkylene oxide which must be employed in a liquid monofuel according to this invention when no alkyl nitrate is used. This minimum is approximately 40% by weight. Two practical considerations determine this minimum. The first consideration is the freezing point of the resultant solution and the second is the stability or shock insensitivity of the resultant solution.
Ethylene oxide, for example, is characterized by a freezing point lower than that of ethylene carbonate, for example, or nitromethane, for example, and its use in substantial proportion is necessary to keep the resulting freezing point of the mixture below approximately 65 F. If the freezing point of the fuel were above this tem perature the fuel would tend to freeze up in certain situations, particularly in high altitude use, which woud be a considerable disadvantage.
With respect to the second consideration, alkylene oxides and ethylene oxide in particular, have a relatively high stability or shock insensitivity, and are relatively difficult to explode. Therefore, when alkyl nitrates, such as n-propyl nitrate, are substituted for them, this substitution is ordinarily only partial. Nitromethane and ethylene carbonate, as examples of nitroalkanes and alkylene oxides respectively, however, are relatively easy to explode and difficult to handle. It follows that substantial proportions of ethylene oxide or its equivalent should be employed so that the resulting fuel will be safe to handle. For example, preferable ranges in this liquid monofuel composition are by weight: 4080% ethylene oxide, 530% nitramethane, and 5-30% ethylene carbonate.
The combination of an alkylene oxide such as ethylene oxide, an alkylene carbonate such as ethylene carbonate,
ate or propylene carbonate.
tures or as an individual species such as ethylene carbon- They may also be entirely onntted from the fuel composition.
Nitroalkanes may also be used in the liquid monofuel of this invention. They may be used as mixtures or as an individual species such as nitromethane, nitroethane,-a nitropropane or a nitrobutane. The combination witha major proportion of an alkylene oxide of substantially equal proportions by weight of nitroalkane and alkylene carbonate constitutes the preferred form of the invention. They may also be entirely omitted from the fuel composition.
The following detailed examples illustrate specific fuel compositions according to this invention. The various components of the compositions according to this invention. The various components of the compositions are generally readily replaced by the several alternativecomponents described above. I
Example 1 A specific preferred example of a liquid monofuel having a decomposition temperature of approximately 1800' F. and a freezing point of approximately 65 F., comprising 2 5% ethylene carbonate, 25% nitromethaneand Example 2 A specific example of a solution having a freezing point of approximately 100 F. and a decomposition temperature of approximately 1800 F., is 10% ethylene carbonand a nitroalkane such as nitromethane, forms a true solution which is miscible in'all proportions of the three elements, as is essential for a satisfactory liquid monopropellant. Because of this complete miscibility, the considerations taken into account when the fuel is prepared are the properties which it is desired to attain, and particularly the exact decomposition temperature required.
The following examples illustrate various combinations which comprise a liquid monofuel according to this invention.
Ordinarily, a major proportion of the fuel comprises one or more alkylene oxides. Such oxides may, for example, be selected from the group comprising ethylene oxide, propylene oxide, 1,3 butadiene dioxide and related diene and triene oxides and dioxides of the lower order olefins and parafiins.
To a considerable extent alkyl nitrates may be substituted for a portion of the alkylene oxides. Among these compounds are methyl nitrate, ethyl nitrate, n-propyl nitrate, isopropyl nitrate and various butyl nitrates such as n-butyl nitrate. Indeed, for some purposes the simple binary combination of an alkylene oxide, such as ethylene oxide, with an alkyl nitrate, such as n-propyl nitrate, will form a satisfactory liquid monofuel. For example, the binary composition can comprise fifty percent of each. Ordinarily, some alkylene oxide is used in combination with the other fuel components of this invention even when it is largely replaced by alkyl nitrate, since the alkylene oxides reduce the danger of explosions in handling. Moreover, various combinations of alkyl nitrate may be used as a fuel component as well as afsingle species. I I
Alkylene carbonates may also be used in the liquid monofuel of this invention. They may be used as mixate, 10% nitromethane and ethylene oxide, all proportions being by weight.
Example 3 A decomposition temperature of approximately 2200 F. is obtained with a liquid monofuel comprising 20% by weight of nitromethane, 5% by weight ethylene canbonate and 75% by weight ethylene oxide. Although a fuel decomposition temperature of about l800 F. is preferred for flight of substantial duration, a decomposition temperature may rise as high as about 2200 F. for short flights. For such situations it is merely necessary to increase the nitromethane content relative to the ethylene carbonate by amounts such that the desired decomposition temperature will be achieved.
Example 4 It may be desirable to lower the decomposition temperature of a liquid monofuel to approximately 1200 F. when a fuel is used to run a gas producer for tank pressurization. To achieve such a temperature it'is necessary to increase the proportion of ethylene carbonate relative to nitromethane. A 1200 F. decomposition solution may be achieved by employing 5% nitromethane, 25% ethylene carbonate and 70% ethylene oxide in proportion by weight.
In summary the principle of the invention relates to the method of varying the decomposition temperature of a solution by varying the proportions of its components such as alkylene carbonate and nitroalkane relative to one another. The resulting solution has improved characteristics relative to autoignition, storage density and vapor pressure. A second principle of the invention relates to the method of varying the proportion of alkylene oxide in a liquid monofuel to change the freezing point of the resulting solution, the main consideration being to employ as little alkylene oxide as possible and yet achieve a sufliciently low freezing point.
There have thus been described various liquid monofuel compositions useful in gas turbine engines and rocket reaction chambers and methods of adjusting the decom position and storage characteristics of these compositions.
What is claimed is:
1. A fuel composition mixture consisting essentially of a major proportion by weight of at least one component selected from the group consisting of lower alkylene oxides and lower alkyl nitrates and a minor proportion by weight of at least one component selected from the group consisting of lower alkylene carbonates and lower nitro alkanes.
2. A fuel composition consisting essentially of a major proportion by weight of at least one lower alkylene oxide and at least one lower alkyl nitrate and a minor proportion by weight of at least one lower alkylene carbonate and at least one lower nitroalkane.
3. A fuel composition consisting essentially of a major proportion by weight of at least one lower alkylene oxide and a minor proportion by weight of at least one lower alkylene carbonate and at least one lower nitroalkane.
4. A fuel composition consisting essentially of a major proportion by weight of at least one lower alkylene oxide and a minor proportion by weight of at least one lower alkylene carbonate.
5. A fuel composition consisting essentially of a major proportion by weight of at least one lower alkylene oxide and a minor proportion by weight of at least one lower nitroalkane.
6. A fuel composition consisting essentially of a major proportion by weight of at least one lower alkyl nitrate and a minor proportion by weight of at least one lower alkylene carbonate and at least one lower nitroalkane.
7. A fuel composition consisting essentially of a major proportion by weight of at least one lower alkyl nitrate and a minor proportion by weight of at least one lower alkylene carbonate.
8. A fuel composition consisting essentially of a major proportion by weight of at least one lower alkyl nitrate and a minor proportion by weight of at least one lower nitroalkane.
9. A fuel composition consisting essentially of a major proportion by weight of ethylene oxide and a minor proportion by weight of nitromethane.
10. A fuel composition consisting essentially of a major proportion by weight of propylene oxide and a minor proportion by weight of nitromethane.
11. A liquid monopropellant for use in combustors 6 consisting essentially of a major proportion by weight of ethylene oxide, and a minor proportion by weight of ethylene carbonate and nitromethane.
12. A liquid monopropellant for use in jet and rocket combustors, consisting essentially of a major proportion by weight of ethylene oxide and a minor proportion by weight of both ethylene carbonate and nitromethane, the proportions of the ethylene carbonate and nitromethane relative to each other being selected to achieve the decomposition temperature required for the combustor in which the monopropellant is to be employed.
13. A liquid monopropellant for use as a rocket and gas turbine fuel, consisting essentially of a major proportion of ethylene oxide, the balance being ethylene carbonate :and nitromethane in substantially equal proportions by weight.
14. A gas turbine and rocket fuel, consisting essentially of the following ingredients and proportions by weight: ethylene oxide, 25% nitromethane, 25% ethylene carbonate.
15. A gas turbine and rocket fuel, consisting essentially of the following ingredients and proportions by weight: 80% ethylene oxide, 10% nitromethane, 10% ethylene carbonate.
16. A gas turbine and rocket fuel, consisting essentially of the following ingredients and proportions by weight: ethylene oxide, 20% nitromethane and 5% ethylene carbonate.
17. A rocket and gas turbine fuel, consisting essentially of the following ingredients in proportions by weight: 70% ethylene oxide, 5% nitromethane, 25% ethylene carbonate.
18. A liquid monopropellant consisting essentially of the following ingredients in proportions by weight: 40- ethylene oxide, 530% nitromethane and 5-30% ethylene carbonate.
19. A liquid monopropellant consisting essentially of the following ingredients in the following proportions by weight: 5080% ethylene oxide, 1025% nitromethane and 10-25% ethylene carbonate, the proportion of nitromethane being substantially equal to the proportion of ethylene carbonate,
No references cited.
Claims (1)
1. A FUEL COMPOSITION MIXTURE CONSISTING ESSENTIALLY OF A MAJOR PROPORTION BY WEIGHT OF AT LEAST ONE COMPONENT SELECTED FROM THE GROUP CONSISTING OF LOWER ALKYLENE OXIDES AND LOWER ALKYL NITRATES AND A MINOR PROPORTION BY WEIGHT OF AT LEAST ONE COMPONENT SELECTED FROM THE GROUP CONSISTING OF LOWER ALKYLENE CARBONATES AND LOWER NITRO ALKANES.
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US536054A US2993768A (en) | 1955-09-22 | 1955-09-22 | Liquid monofuel and method of forming |
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
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US3208891A (en) * | 1964-03-02 | 1965-09-28 | Olin Mathieson | Monopropellant comprising an alkyl nitrate and a nitroparaffin additive |
US3257470A (en) * | 1963-09-16 | 1966-06-21 | William L Gilliland | Nitrocompounds |
US3377219A (en) * | 1964-09-28 | 1968-04-09 | Army Usa | Nitrated organic liquid propellant composition having improved spark ignition |
US4157928A (en) * | 1973-03-01 | 1979-06-12 | The United States Of America As Represented By The Secretary Of The Navy | Method for fuel air explosive |
US4302208A (en) * | 1980-05-01 | 1981-11-24 | The United States Of America As Represented By The Secretary Of The Navy | Gelled FAE fuel |
US6272846B1 (en) | 1999-04-14 | 2001-08-14 | The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration | Reduced toxicity fuel satellite propulsion system |
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1955
- 1955-09-22 US US536054A patent/US2993768A/en not_active Expired - Lifetime
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Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3257470A (en) * | 1963-09-16 | 1966-06-21 | William L Gilliland | Nitrocompounds |
US3208891A (en) * | 1964-03-02 | 1965-09-28 | Olin Mathieson | Monopropellant comprising an alkyl nitrate and a nitroparaffin additive |
US3377219A (en) * | 1964-09-28 | 1968-04-09 | Army Usa | Nitrated organic liquid propellant composition having improved spark ignition |
US4157928A (en) * | 1973-03-01 | 1979-06-12 | The United States Of America As Represented By The Secretary Of The Navy | Method for fuel air explosive |
US4302208A (en) * | 1980-05-01 | 1981-11-24 | The United States Of America As Represented By The Secretary Of The Navy | Gelled FAE fuel |
US6272846B1 (en) | 1999-04-14 | 2001-08-14 | The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration | Reduced toxicity fuel satellite propulsion system |
US6311477B1 (en) | 1999-04-14 | 2001-11-06 | The United States Of America As Represented By The Administrator Of The National Aeronautics Space Administration | Reduced toxicity fuel satellite propulsion system including axial thruster and ACS thruster combination |
US6314718B1 (en) | 1999-04-14 | 2001-11-13 | The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration | Reduced toxicity fuel satellite propulsion system including fuel cell reformer with alcohols such as methanol |
US6378291B1 (en) | 1999-04-14 | 2002-04-30 | The United States Of America As Represented By The Administrator Of The National Aeronatics And Space Administration | Reduced toxicity fuel satellite propulsion system including catalytic decomposing element with hydrogen peroxide |
US6546714B1 (en) | 1999-04-14 | 2003-04-15 | The United States Of America, As Represented By The Administrator Of The National Aeronautics And Space Administration | Reduced toxicity fuel satellite propulsion system including plasmatron |
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