HYPERGOLIC HYDROCARBON FUEL

Abstract

The present application generally relates to hypergolic hydrocarbon fuel compositions comprising a convenient fuel and a cycloheptatriene and/or its analogs, and methods of making and using the hypergolic hydrocarbon fuel compositions.

Claims

1. A hypergolic fuel composition comprising a conventional fuel and a compound of formula (I): ##STR00003## wherein R.sup.1-R.sup.8 are each independently H, NR.sup.9R.sup.10, OR.sup.11, NH(CO)R.sup.12, O(CO)R.sup.13, CN, NO.sub.2, CF.sub.3, (CO)R.sup.14, COOR.sup.15, halogen, C1-C8 straight or branched alkyl, C1-C8 straight or branched alkenyl, C1-C8 straight or branched alkynyl, or C3-C8 cycloalkyl, and wherein R.sup.1 and R.sup.2 can form an exocyclic double bond X, wherein X is CR.sup.16R.sup.17, NR.sup.18, or O; and R.sup.9-R.sup.18 are each independently H, C1-C8 straight or branched alkyl, wherein the hypergolic fuel composition provides an ignition delay of 1 ms-100 ms when the hypergolic fuel composition is treated with an oxidizer.

2. The fuel composition of claim 1, wherein the compound of formula (I) is cycloheptatriene.

3. The fuel composition of claim 1, wherein the weight percentage of the compound of formula (I) is 1-99.9%.

4. The fuel composition of claim 1, wherein the conventional fuel comprises kerosene.

5. A method for producing a hypergolic propellant comprising contacting a hypergolic fuel with an oxidizer, wherein said hypergolic fuel comprises a compound of formula (I): ##STR00004## wherein R.sup.1-R.sup.8 are each independently H, NR.sup.9R.sup.10, OR.sup.11, NH(CO)R.sup.12, O(CO)R.sup.13, CN, NO.sub.2, CF.sub.3, (CO)R.sup.14, COOR.sup.15, halogen, C1-C8 straight or branched alkyl, C1-C8 straight or branched alkenyl, C1-C8 straight or branched alkynyl, or C3-C8 cycloalkyl, and wherein R.sup.1 and R.sup.2 can form an exocyclic double bond X, wherein X is CR.sup.16R.sup.17, NR.sup.18, or O; and R.sup.9-R.sup.18 are each independently H, C1-C8 straight or branched alkyl.

6. The method of claim 5, wherein the hypergolic fuel comprises cycloheptatriene.

7. The method of claim 5, wherein the hypergolic fuel further comprises a conventional fuel.

8. The method of claim 5, wherein the conventional fuel comprises kerosene.

9. The method of claim 5, wherein the oxidizer comprises N.sub.2O.sub.4, NO, or a combination thereof.

10. The method of claim 5, wherein the method provides an ignition delay of 1 ms-50 ms.

Description

DETAILED DESCRIPTION

[0013] For the purposes of promoting an understanding of the principles of the present disclosure, reference will now be made to the embodiments illustrated in the drawings, and specific language will be used to describe the same. It will nevertheless be understood that no limitation of the scope of this disclosure is thereby intended.

[0014] In the present disclosure the term about can allow for a degree of variability in a value or range, for example, within 10%, within 5%, or within 1% of a stated value or of a stated limit of a range.

[0015] In the present disclosure the term substantially can allow for a degree of variability in a value or range, for example, within 90%, within 95%, or within 99% of a stated value or of a stated limit of a range.

[0016] A hypergolic propellant used in a rocket engine usually comprises two components that can spontaneously ignite when they come into contact with each other.

[0017] The two propellant components usually comprises a fuel and an oxidizer. Although commonly used hypergolic propellants are difficult to handle because of their extreme toxicity and/or corrosiveness, they can be stored as liquids at room temperature and hypergolic engines are easy to ignite reliably and repeatedly.

[0018] In contemporary usage, the terms hypergol and/or hypergolic propellant usually mean the most common such propellant combinations, such as dinitrogen tetroxide plus hydrazine and/or its relatives monomethylhydrazine and unsymmetrical dimethylhydrazine.

[0019] Both unsymmetrical dimethylhydrazine and monomethylhydrazine are confirmed animal carcinogens that have been characterized as tumorigenic, mutagenic, reproductive effectors.

[0020] This extreme toxicity and the associated difficulties and expense of transporting and handling these compounds have produced widespread interest in finding replacement fuels.

[0021] There is, therefore an unmet need for safer and more convenient hypergolic fuel compositions and methods to make and use of the hypergolic fuel compositions.

[0022] To become an acceptable hypergolic fuel, a hypergolic fuel should not only provide robust burning capability, but also should have a desire ignition delay time. In addition, a good hypergolic fuel should be miscible with some other conventional fuel such as kerosene.

[0023] The present disclosure therefore provides a hypergolic fuel composition that exhibit these advantages.

[0024] In one embodiment, the present invention provides a hypergolic fuel composition comprising a conventional fuel and a compound of formula (I):

##STR00002##

wherein R.sup.1-R.sup.8 are each independently H, NR.sup.9R.sup.10, OR.sup.11, NH(CO)R.sup.12, O(CO)R.sup.13, CN, NO.sub.2, CF.sub.3, (CO)R.sup.14, COOR.sup.15, halogen, C1-C8 straight or branched alkyl, C1-C8 straight or branched alkenyl, C1-C8 straight or branched alkynyl, or C3-C8 cycloalkyl, and wherein R.sup.1 and R.sup.2 can form an exocyclic double bond X, wherein X is CR.sup.16R.sup.17, NR.sup.18, or O; and R.sup.9-R.sup.18 are each independently H, C1-C8 straight or branched alkyl.

[0025] In one embodiment, the present invention provides a hypergolic fuel composition comprising a conventional fuel and a compound of formula (I), wherein R.sup.1-R.sup.8 are each independently H, NR.sup.9R.sup.10, OR.sup.11, NH(CO)R.sup.12, O(CO)R.sup.13, CN, NO.sub.2, CF.sub.3, (CO)R.sup.14, COOR.sup.15, halogen, C1-C4 straight or branched alkyl, C1-C4 straight or branched alkenyl, C1-C4 straight or branched alkynyl, or C3-C7 cycloalkyl, and wherein R.sup.1 and R.sup.2 can form an exocyclic double bond X, wherein X is CR.sup.16R.sup.17, NR.sup.18, or O; and R.sup.9-R.sup.18 are each independently H, C1-C4 straight or branched alkyl.

[0026] In one embodiment, the present invention provides a hypergolic fuel composition comprising a conventional fuel and a compound of formula (I), wherein R.sup.1-R.sup.8 are each independently H, NR.sup.9R.sup.10, OR.sup.11, CN, NO.sub.2, CF.sub.3, COOR.sup.15, halogen, C1-C4 straight or branched alkyl, C1-C4 straight or branched alkenyl, C1-C4 straight or branched alkynyl, or C3-C7 cycloalkyl, and wherein R.sup.1 and R.sup.2 can form an exocyclic double bond X, wherein X is CR.sup.16R.sup.17, NR.sup.18, or O; and R.sup.9-R.sup.18 are each independently H, C1-C4 straight or branched alkyl

[0027] In one embodiment, the present invention provides a hypergolic fuel composition comprising a salt formed by the deprotonation of a compound of formula (I), wherein at least one of R.sup.1 and R.sup.2 is hydrogen in the compound of formula (I) before the compound of formula (I) is deprotonated. The counter ion can be any suitable counter ion including but is not limited to F, Cl.sup., Br.sup., I.sup., OH.sup., CN.sup., NO.sub.3.sup., HCO.sub.3.sup..

[0028] In one embodiment, the present invention provides a hypergolic fuel composition comprising a conventional fuel and a compound of formula (I), wherein R.sup.1-R.sup.8 are H.

[0029] In one embodiment, the present invention provides a hypergolic fuel composition comprising a conventional fuel and a compound of formula (I), wherein the conventional fuel is a traditional energy sources or fossil fuels such as petroleum, oil, coal, propane, kerosene, and natural gas. In one embodiment, the conventional fuel is kerosene.

[0030] The oxidizers typically used with fuels to provide a hypergolic bipropellant system include but is not limited to nitrogen tetroxide (N.sub.2O.sub.4), nitric oxide (NO), nitric acid (HNO.sub.3), or any combination thereof.

[0031] In one embodiment, the present disclosure provides that the mass ratios of oxidizer-to-fuel will typically range from 1:10 to 10:1.

[0032] In one embodiment, the present disclosure provides that the weight percentage of the compound of formula (I) in the hypergolic fuel composition is about 5.0-99.9 wt %. In one embodiment, the weight percentage of the compound of formula (I) in the hypergolic fuel composition is about 10.0-99.9 wt %. In one embodiment, the weight percentage of the compound of formula (I) in the hypergolic fuel composition is about 20.0-99.9 wt %. In one embodiment, the weight percentage of the compound of formula (I) in the hypergolic fuel composition is about 30.0-99.9 wt %. In one embodiment, the weight percentage of the compound of formula (I) in the hypergolic fuel composition is about 40.0-99.9 wt %. In. one embodiment, the weight percentage of the compound of formula (I) in the hypergolic fuel composition is about 50.0-99.9 wt %. In one embodiment, the weight percentage of the compound of formula (I) in the hypergolic fuel composition is about 60.0-99.9 wt %. In one embodiment, the weight percentage of the compound of formula (I) in the hypergolic fuel composition is about 70.0-99.9 wt %. In one embodiment, the weight percentage of the compound of formula (I) in the hypergolic fuel composition is about 90.0-99.9 wt %. In one embodiment, the weight percentage of the compound of formula (I) in the hypergolic fuel composition is about 90.0-99.9 wt %.

[0033] In one embodiment, the present disclosure provides that the compound of formula (I) is miscible with the conventional fuel. In one aspect, the compound of formula (I) is miscible with kerosene.

[0034] In one embodiment, the present disclosure provides that the compound of formula (I) may provide an ignition delay of 1 ms-200 ms. In one aspect, the compound of formula (I) may provide an ignition delay of 1 ms-100 ms. In one aspect, the compound of formula (I) may provide an ignition delay of 1 ms-50 ms. In one aspect, the compound of formula (I) may provide an ignition delay of 5 ms-25 ms.

[0035] In one In one embodiment, the present disclosure provides a method for producing a hypergolic propellant comprising contacting a hypergolic fuel with an oxidizer wherein said hypergolic fuel comprises a compound represented by the formula (I). In one aspect, the oxidizer may be selected but is not limited to nitrogen tetroxide (N.sub.2O.sub.4), nitric acid (HNO.sub.3), or a mixture such as MON-25, which is N.sub.2O.sub.4 with 25% nitric oxide (NO), or any combination thereof.

Example

[0036] The compound of formula (I) is either used as pure form or mixed with one or more appropriate conventional fuel such as kerosene. Cycloheptatriene (CHT) is an exemplary fuel of the present disclosure. The weight percentage of CHT in the CHT/conventional fuel mixture may be in the range of 5-100%.

[0037] Liquid nitrogen tetroxide (NTO) is condensed in a water chilled condenser. The stopper is raised to allow a single drop of NTO to fall onto the fuel. About 3 drops of a fuel sample are contained in a vial 5 inches below the bottom of the condenser. The vial is set centered on a micrometer x-y stage. The event is illuminated by LEDs and filmed by a Vision Research Phantom V1212 high speed color camera. Analysis of the high speed video determines the ignition delay, defined as the time from first liquid contact to the first emission of visible light. The camera films at 10,000 frames per second, providing0.1 ms uncertainty on contact and the same on flame emission. The total uncertainty of the ignition delay measurement is thus0.2 ms.

TABLE-US-00001 TABLE 1 Hypergolic reaction of cycloheptatriene (CHT) with liquid nitrogen tetroxide (NTO) (Reaction was carried out under ambient pressure and at 15 C. All fuels were purchased from chemical suppliers (i.e. Sigma-Aldrich, etc.) and used as is). Ignition Delay Chemical Name Notes on Reaction (ms) Cycloheptatriene Bright carbon flame, low 18.7 (n1 = 14.8, (CHT) (100%) whoosh as opposed to strong n2 = 23.8, pop, ignition on 3/3 tests n3 = 17.5)

TABLE-US-00002 TABLE 2 Hypergolic Reaction between cycloheptatriene (CHT) composition (with or without kerosene) and liquid nitrogen tetroxide (NTO) or MON-25 (N2O4 with 25% nitric oxide). The reaction was carried out at 80 psi (5.5 atm) Wt. % Freezing Point Boiling Point Ignition Delay, Ignition Delay, CHT ( C.) ( C.) MON-25 (ms) NTO (ms) 100 67 115 6.1 23.8 80 89 127 14.5 no reaction 20 81 193 29.7 no reaction

[0038] The results demonstrate that CHT or CHT/kerosene mixture can react with NTO and/or MON-25 at appropriate conditions to provide ignition delay that may be sufficient as desired hypergolic fuel compositions.

[0039] In addition, CHT demonstrated excellent miscibility with kerosene. The mixture of CHT and kerosene has lower freezing point and higher boiling point comparing to pure form of CHT. The lower freezing point and higher boiling point are desired for hypergolic fuels because the broader temperature range may provide more convenient applications at a wide variety of conditions.

[0040] Those skilled in the art will recognize that numerous modifications can be made to the specific implementations described above. The implementations should not be limited to the particular limitations described. Other implementations may be possible.