High performance, low toxicity hypergolic fuel

Information

  • Patent Grant
  • 8685186
  • Patent Number
    8,685,186
  • Date Filed
    Wednesday, January 23, 2013
    11 years ago
  • Date Issued
    Tuesday, April 1, 2014
    10 years ago
Abstract
A group of tertiary amine azides are useful as hypergolic fuels for hypergolic bipropellant mixtures. The fuels provide higher density impulses than monomethyl hydrazine (MMH) but are less toxic and have lower vapor pressures that MMH. In addition, the fuels have shorter ignition delay times than dimethylaminoethylazide (DMAZ) and other potential reduced toxicity replacements for MMH.
Description
BACKGROUND OF THE INVENTION

1. Field of the Invention


The present invention relates to a hypergolic rocket fuels that simultaneously possess high-performance propellant characteristics and low toxicity relative to Monomethylhydrazine (MMH). The fuels provide propellant performance as high as or higher than MMH, but have lower toxicity.


2. Description of Related Art


Monomethylhydrazine (MMH) is a widely employed fuel in hypergolic, bipropellant systems. MMH possesses desirable propellant properties but it is highly toxic, carcinogenic, and corrosive. Although gelling has dramatically improved the safety of handling and storing the propellant, its toxicity and carcinogenicity are still of major concern. Therefore, there is a need for alternative liquid hypergolic fuels that are less carcinogenic and less toxic than MMH but also have equal or higher energy densities, lower vapor pressures and ignition delays than MMH. These fuels, like MMH, may be used in the form of gels to further improve safety.


Although DMAZ is hypergolic, its ignition delay with IRFNA is significantly longer than MMH. A longer ignition delay requires a larger combustion chamber to avoid pressure spikes that can damage the engine.


U.S. Pat. No. 6,013,143 discloses three chemicals, each comprising a tertiary nitrogen and an azide functional group that are hypergolic when mixed with an oxidizer such as IRFNA, hydrogen peroxide, nitrogen tetroxide, and hydroxyl ammonium nitrate. The chemicals are dimethylaminoethylazide (DMAZ), pyrollidineylethylazide (PYAZ), and bis (ethyl azide)methylamine (BAZ). Inhibited Red Fuming Nitric Acid (IRFNA) type IIIB and monomethyl hydrazine (MMH) deliver a specific impulse of 284 lbf sec/lbm and a density impulse of 13.36 lbf sec/cubic inch in a rocket engine operating a pressure of 2000 psi. DMAZ, PYAZ, and BAZ are proposed as potential replacements for MMH. DMAZ, under the same conditions as MMH, delivers a specific impulse of 287 lbf sec/Ibm and a density impulse of 13.8 lbf sec/cubic inch. The patent discloses the mixing of the hypergolic fuel chemicals with gellants and additives such as aluminum and boron to increase specific impulse and density impulse values.


U.S. Pat. No. 6,926,633 discloses a family of amine azides having cyclic structures and for use as hypergolic rocket propellants. The amine azide compounds comprise at least one amine, including tertiary amines, and an azide functional group pendant from a cyclic structure. The propellants are disclosed as being used with oxidizers and, optionally with catalysts present in fuel or oxidizer. Fuel properties for the amine azides are provided based on computational quantum chemistry calculations.


U.S. Pat. No. 6,949,152 discloses hypergolic propulsion systems comprising a fuel composition and an oxidizer composition. The fuel composition contains an azide compound having at least one tertiary nitrogen and at least one azide functional group. The oxidizer contains hydrogen peroxide in water. The hypergolic reaction between oxidizer and fuel is catalyzed by a transition metal, preferably compounds of cobalt and manganese.


Unlike hypergolic fuels disclosed previously, the present fuels exhibit lower toxicity and higher performance than MMH. The fuels require no catalyst to achieve high performance and are hypergolic with commonly used oxidizers. The fuels of the present invention may be used alone, in combination with each other, or in combination with other fuels in blends.


BRIEF SUMMARY OF THE INVENTION

The present invention is a group of tertiary amine azide chemicals useful as hypergolic fuels for hypergolic bipropellant mixtures. The fuels provide higher density impulses than MMH but are less toxic and have lower vapor pressures that MMH. In addition, the fuels have shorter ignition delay times than DMAZ and other potential reduced toxicity replacements for MMH.







DETAILED DESCRIPTION OF THE INVENTION

The present invention is a rocket fuel composition comprising one or more of the molecules I-XIII.




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The fuel is hypergolic when combined with a strong oxidizer such as IRFNA, hydrogen peroxide, nitrogen tetroxide, or hydroxyl ammonium nitrate. Relevant chemical and physical properties of the molecules have been calculated using validated molecular modeling techniques, including quantum chemistry and Conductor-like Screening MOdel for Real Solvent (COSMO-RS) methods. The fuel molecules have one or more improved propellant properties relative to MMH and DMAZ including heat of formation, density, vapor pressure, absence of N—N single bonds, and short ignition delay.


Heats of Formation


First-principle ab initio quantum chemistry methods are the most accurate and suitable technique for calculations of molecular geometries, heats of formations, and activation barriers. The procedure numerically solves a many-electron Schrödinger equation to obtain a molecular wave function and energy. The molecular energies can be used to calculate heats of formation.


CBS-QB3 combined with isodesmonic reaction methods were used to calculate heats of formations and activation barriers. Heat of vaporization was calculated using a COSMO-RS technique. Table 1 shows the computed heats of formation for hydrazine, MMH, DMAZ, and compounds I-XIII. Numbers in parentheses are National Institutes of Standards and Technology (NIST) experimental data. The molecules of the present invention possess higher heats of formation than MMH, and are therefore expected to possess specific impulse values that exceed those for MMH.









TABLE 1







Computed Heats of Formation and Densities















Predicted



Gas Phase
Gas Phase
Predicted
Density with


Molecule
ΔHf298K kcal/mol
ΔHf298K cal/gm
Density
Correlation





Hydrazine
23.8 (22.8)
744.9 (712.5)




MMH
23.0 (22.6)
500.9 (492.2)




DMAZ
73.4
643.6




I
96.2
858.9
1.1320
0.9346


II
149.8
1361.9
1.1334
0.9362


III
110.1
781.0
1.2114
1.0246


IV
134.8
1078.2
1.3325
1.1619


V
112.2
738.3
1.4048
1.2438


VI
90.0
489.0
1.2153
1.0290


VII
112.2
679.7
1.3801
1.2158


VIII
110.0
516.3
1.2347
1.0510


IX
114.3
747.2
1.2449
1.0626


X
89.6
577.8
1.1381
0.9415


XI
128.5
537.6
1.3249
1.1532


XII
106.5
578.9
1.2433
1.0608


XIII
144.6
510.9
1.2539
1.0728









Densities


Once the molecular volume is known, the density can be computed using molecular weight. Molecular volume, defined as the volume occupied by 0.001 au (1 au=6.748 e/Angstrom) electron density envelope, was calculated for eah of I-XIII. Calculated and known densities were compared for a number of amines and amine azides to validate density calculations. Calculations were performed at the PBEPBE/6-311++G(d,p) level. Table 1 shows calculated densities with and without a corective correlation.


Density Impulses


Specific and density impulse are the two most important parameters describing the performance of a fuel. Density impulse is a measure of the performance per volume of the fuel. Table 2 shows the computed specific and density impulse for each of the molecules I-XIII with IRFNA as the oxidizer.









TABLE 2







Computed Specific and Density Impulse












Density Impulse
%



Specific Impulse
density*Isp*10−3
Improvement over


Molecule
Isp (lbf-sec/lbm)
(lbf-sec/ft3)
MMH













I
280.0
16.3
4.1


II
286.4
16.7
6.6


III
280.2
17.9
14.2


IV
280.7
20.4
29.7


V
272.4
21.2
34.7


VI
276.8
17.8
13.3


VII
267.8
20.3
29.5


VIII
278.0
18.2
16.2


IX
283.4
18.8
19.7


X
277.5
16.3
3.9


XI
277.6
20.0
27.3


XII
279.0
18.5
17.7


XIII
278.4
18.6
18.8









The Isp values were calculated using the PROPEP thermochemical code and correspond to the optimum fuel/IRFNA ratio.


Synthesis of Hypergolic Fuels


The molecules of the present invention may be synthesized by those skilled in the art using known chemical synthetic reactions. For example, the synthesis of compound V can be accomplished by the using the known condensation of guanidines with haloacetates followed by reaction with PCl5 and treatment with NaN3. Compound VII can be prepared from 2,4-dichlorotriazine by sequential substitution of the chlorine atoms. The dichloride 5 can be prepared by condensation of iminyl chloride. The preparation of compound XII can be accomplished, for example, by transamination between two symmetric triazinanes.

Claims
  • 1. A hypergolic bipropellant combination comprising an oxidizer and a fuel, said fuel comprising an amine azide chemical having the structure:
  • 2. The hypergolic bipropellant combination of claim 1, further comprising a gellant mixed with the fuel or the oxidizer.
  • 3. The hypergolic bipropellant combination of claim 1, wherein the oxidizer is selected from IRFNA, hydrogen peroxide, nitrogen tetroxide, and hydroxyl ammonium nitrate.
  • 4. The hypergolic bipropellant combination of claim 1, wherein the fuel is a mixture comprising the amine azide chemical as an additive.
  • 5. The hypergolic bipropellant combination of claim 1, comprising at least a second amine azide chemical having a structure of one of structures I, II, III, IV, V, VI, VII, VIII, IX, X, XI, XII, or XIII:
  • 6. The hypergolic bipropellant combination of claim 5, further comprising a gellant mixed with the fuel or the oxidizer.
  • 7. The hypergolic bipropellant combination of claim 5, wherein the oxidizer is selected from IRFNA, hydrogen peroxide, nitrogen tetroxide, and hydroxyl ammonium nitrate.
  • 8. The hypergolic bipropellant combination of claim 5, wherein the fuel is a mixture comprising the amine azide chemical as an additive.
CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional of application Ser. No. 12/781,842, filed May 18, 2010, which is a divisional of application Ser. No. 11/679,672, filed Feb. 27, 2007 now U.S. Pat. No. 7,749,344, which patents and applications are incorporated herein by specific reference in their entirety.

FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

This invention was made with Government support under contract W31P4Q-06-C-0167 awarded by the US Army. The Government has certain rights in this invention.

US Referenced Citations (8)
Number Name Date Kind
3971681 Rains et al. Jul 1976 A
6013143 Thompson Jan 2000 A
6210504 Thompson Apr 2001 B1
6962633 McQuaid Nov 2005 B1
7749344 Sengupta Jul 2010 B2
8382922 Sengupta Feb 2013 B2
20050022911 Rusek et al. Feb 2005 A1
20080127551 Stevenson, III et al. Jun 2008 A1
Related Publications (1)
Number Date Country
20130133242 A1 May 2013 US
Divisions (2)
Number Date Country
Parent 12781842 May 2010 US
Child 13748480 US
Parent 11679672 Feb 2007 US
Child 12781842 US