US3219500A - Fuel comprising a hydrazinoalkane and hydrazines - Google Patents

Fuel comprising a hydrazinoalkane and hydrazines Download PDF

Info

Publication number
US3219500A
US3219500A US202346A US20234662A US3219500A US 3219500 A US3219500 A US 3219500A US 202346 A US202346 A US 202346A US 20234662 A US20234662 A US 20234662A US 3219500 A US3219500 A US 3219500A
Authority
US
United States
Prior art keywords
hydrazine
fuel
weight percent
hydrazinoalkane
mixtures
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
Application number
US202346A
Inventor
Calvin E Pannell
Phyllis D Oja
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Dow Chemical Co
Original Assignee
Dow Chemical Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Dow Chemical Co filed Critical Dow Chemical Co
Priority to US202346A priority Critical patent/US3219500A/en
Application granted granted Critical
Publication of US3219500A publication Critical patent/US3219500A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B47/00Compositions in which the components are separately stored until the moment of burning or explosion, e.g. "Sprengel"-type explosives; Suspensions of solid component in a normally non-explosive liquid phase, including a thickened aqueous phase
    • C06B47/02Compositions in which the components are separately stored until the moment of burning or explosion, e.g. "Sprengel"-type explosives; Suspensions of solid component in a normally non-explosive liquid phase, including a thickened aqueous phase the components comprising a binary propellant
    • C06B47/08Compositions in which the components are separately stored until the moment of burning or explosion, e.g. "Sprengel"-type explosives; Suspensions of solid component in a normally non-explosive liquid phase, including a thickened aqueous phase the components comprising a binary propellant a component containing hydrazine or a hydrazine derivative

Definitions

  • Anhydrous hydrazine is a desirable fuel for liquid propellant systems for rocket motors since it reacts spontaneously with certain oxidizers, e.g. nitric acid and concentrated hydrogen peroxide, thereby forming a noncarbonaceous propellant system.
  • this fuel which has a density of about 1.01 g./c-rn. also has an undesirably high freezing point of about 34 F. Therefore, to extend operable temperature range for using this fuel at lower temperatures it is ordinarily used as a mixture with uns-dimethyl hydrazine (UDMH) or monomethylhydrazine (MMH), for example, ordinarily at a 50-50 weight ratio.
  • UDMH uns-dimethyl hydrazine
  • MMH monomethylhydrazine
  • the present invention provides a liquid propellant fuel composition having a density greater than anhydrous hydrazine, a desirably low freezing point and exhibiting substantially the same high specific impulse as shown by hydrazine itself.
  • This fuel composition of this invention comprises a hydrazinoalkane mixed with a member selected from the group consisting of hydrazine, mono and dimethyl substituted hydrazine and mixtures thereof.
  • hydrazinoalkane refers to those compounds corresponding to the general formula designated hereinafter as EDH, is employed in the composition in admixture with hydrazine.
  • EDH the general formula designated hereinafter as EDH
  • the hereinbefore stated advantages are obtained, for example, utilizing a mixture containing from about 5 to about 95 weight percent EDH and from about 95 to about 5 weight percent substantially anhydrous hydrazine. Mixtures containing more than about 95 Weight percent EDH display a high viscosity which makes pumping of the mixture somewhat diflicult.
  • the fuel composition will contain from about 20 to about 80 weight percent EDH, balance hydrazine and preferably a 50-50 weight percent composition is used.
  • hydrazinoalkane to hydrazine- UMDH or other hydrazine containing liquid propellant fuel mixtures also provides both depressed freezing of the liquid and increased density advantage to such mixtures.
  • a ternary mixture of from about 10 to weight percent UMDH, about 40 to weight percent hydrazine and about 5 to 50 Weight percent EDH provide a satisfactory liquid propellant.
  • this ternary composition will contain about equal parts by weight of the three components.
  • the excess aqueous hydrazine is removed, eg by distillation, from the product mass, and the hydrazinoalkane product subsequently converted into the acid salt.
  • This salt can be regenerated as the free base, and a purified product recovered by distillation.
  • the propellant fuel composition of the present invention can be employed in a liquid propellant system in the same manner and with the same oxidants as are used for hydrazine alone.
  • Example 1 The freezing point for a number of EDH-anhydrous hydrazine binary mixtures was determined employing standard freezing point determination techniques. The results of these tests are presented in Table I.
  • a 50-50 weight percent mixture of EDH and UDMH can be employed as a fuel in a bipropellant system with hydrogen peroxide oxidizer.
  • a ternary mixture of about equal parts by weight of EDH-UDMH- N I-L can be used as a fuel with a fuming nitric acid oxidant.
  • a mixture of 20 weight percent 1,2,3,4- tetrahydrazinobutane and 80 weight percent hydrazine can be employed as a liquid fuel in a bi-propellant system employing liquid oxygen as an oxidizer.
  • 1,2,3,4,5,6- hexahydrazinohexane can be admixed with hydrazine to provide a propellant fuel having the desired characteristics set forth herein.
  • a liquid propellant fuel comprising in combination a hydrazinoalklane and a member selected from the group consisting of hydrazine, mono and dimethyl substituted hydrazines and mixtures thereof, said hydrazinoalkane being a compound corresponding to the general formula LHI INHQJn wherein n is an integer ranging from 2 to about 6, the amount of said hydrazinoalkane in said composition ranging from about 5 percent, based on the total composition weight, up to an amount wherein said composition becomes too viscous for ready handling.
  • liquid propellant composition consisting essentially of hydrazine, mono and dimethyl hydrazines and mixtures thereof, the improvement which comprises incorporating into said composition at least 5 weight percent of a hydrazinoalkane freezing point depressant and density increaser corresponding to the general formula Elli l LHI INH 2 n wherein n is an integer ranging from 2 to about 6.
  • a liquid propellant composition comprising from about 5 to about 95 weight percent 1,2-dihydrazinoethane and from about 95 to about 5 percent substantialy anhydrous hydrazine.
  • a liquid propellant composition comprising about weight percent 1,2-dihydrazinoethane and about 50 weight percent substantialy anhydrous hydrazine.
  • a liquid rocket propellant comprising from about 10 to about 40 weight percent uns.-dimethylhydrazine, about 40 to about weight percent hydrazine and about 5 to 50 weight percent 1,2-dihydrazinoethane.
  • a liquid propellant fuel which comprises in about equal weight proportions a ternary mixture of uns.-dimethylhydrazine, hydrazine and 1,2-dihydrazinoethane.

Description

United States Patent Office 3,219,500 Patented Nov. 23, 1965 3,219,500 FUEL COMPRISING A HYDRAZINOALKANE AND HYDRAZINES Calvin E. Pannell, Lafayette, and Phyllis D. Oja, Walnut Creek, Calif., assignors to The Dow Chemical Company, Midland, Mich., a corporation of Delaware No Drawing. Filed June 7, 1962, Ser. No. 202,346 6 Claims. (Cl. 149-36) This invention relates to propellant fuels and more particularly is concerned with an improved dense, liquid, nitrogen containing organic fuel for use in liquid bipropellant systems.
Anhydrous hydrazine is a desirable fuel for liquid propellant systems for rocket motors since it reacts spontaneously with certain oxidizers, e.g. nitric acid and concentrated hydrogen peroxide, thereby forming a noncarbonaceous propellant system. However, this fuel, which has a density of about 1.01 g./c-rn. also has an undesirably high freezing point of about 34 F. Therefore, to extend operable temperature range for using this fuel at lower temperatures it is ordinarily used as a mixture with uns-dimethyl hydrazine (UDMH) or monomethylhydrazine (MMH), for example, ordinarily at a 50-50 weight ratio. These mixtures have a freezing point reduced over that of hydrazine alone but also are less dense, e.g., UDMH has a density of about 0.79 g./cm. This decreased density of the mixed fuel is particularly undesirable since volume is of prime consideration in most rocket applications.
Now, unexpectedly the present invention provides a liquid propellant fuel composition having a density greater than anhydrous hydrazine, a desirably low freezing point and exhibiting substantially the same high specific impulse as shown by hydrazine itself.
This fuel composition of this invention comprises a hydrazinoalkane mixed with a member selected from the group consisting of hydrazine, mono and dimethyl substituted hydrazine and mixtures thereof. The term hydrazinoalkane as used herein refers to those compounds corresponding to the general formula designated hereinafter as EDH, is employed in the composition in admixture with hydrazine. With this two component fuel, the hereinbefore stated advantages are obtained, for example, utilizing a mixture containing from about 5 to about 95 weight percent EDH and from about 95 to about 5 weight percent substantially anhydrous hydrazine. Mixtures containing more than about 95 Weight percent EDH display a high viscosity which makes pumping of the mixture somewhat diflicult. Desirably the fuel composition will contain from about 20 to about 80 weight percent EDH, balance hydrazine and preferably a 50-50 weight percent composition is used.
The addition of the hydrazinoalkane to hydrazine- UMDH or other hydrazine containing liquid propellant fuel mixtures also provides both depressed freezing of the liquid and increased density advantage to such mixtures. To illustrate, a ternary mixture of from about 10 to weight percent UMDH, about 40 to weight percent hydrazine and about 5 to 50 Weight percent EDH provide a satisfactory liquid propellant. Preferably, this ternary composition will contain about equal parts by weight of the three components.
The hydrazinoalkanes are prepared by the method described in copending application, Serial No. 202,347, filed even date herewith. This reaction comprises reacting the corresponding halogenated alkane with aqueous hydrazine at a hydrazine hydrate/halogenated alkane molar ratio of from about 10 to 25. This reaction is carried out at ambient pressures over a temperature range of from about 560 C., preferably 3540 C., employing the hydrazine as an aqueous solution containing from about 40 to about 80 weight percent hydrazine. The reaction readily is accomplished in a reactor vessel equipped with a stirring mechanism using intermittent agitation of the reactants during the reaction period. Completion of the reaction is observed by the disappearance of the two phases and formation of a substantially homogeneous reaction mass, the aqueous hydrazine and halogenated hydrocarbon initially being substantially immiscible.
The excess aqueous hydrazine is removed, eg by distillation, from the product mass, and the hydrazinoalkane product subsequently converted into the acid salt. This salt can be regenerated as the free base, and a purified product recovered by distillation.
The propellant fuel composition of the present invention can be employed in a liquid propellant system in the same manner and with the same oxidants as are used for hydrazine alone.
The following examples will serve to illustrate further the present invention, but are not meant to limit it thereto.
Example 1 The freezing point for a number of EDH-anhydrous hydrazine binary mixtures was determined employing standard freezing point determination techniques. The results of these tests are presented in Table I.
TABLE L-FREEZING POINTS OF 1,2-DIHYDRAZINOEIH- ANE ANH. HYDRAZINE MIXTURES Run No. EDH, Wt. Hydrazine, F.P., C.
percent wt. percent In a second series of tests the density at room temperature, about 25 C., of a number of EDH-anhydrous hydrazine mixtures was determined. Table II shows the results of these measurements:
TABLE IL-DENSITIES OF 1,2-DIHYDRAZINOETHANE- ANH. HYDRAZINE MIXTURES EDH, wt. Hydrazine, Density, Run N0 percent wt. percent g., cm.
The viscosity of a number of EDH-anhydrous hydrazine mixtures was determined using a Gardner-Holdt viscome- 3 ter tube. The measurements were taken at 25 C. The results of these studies are presented in Table III.
TABLE IIL-VISCOSI'IIES OF 1,2-DIHYDRAZINOETHANE- ANH. HYDRAZINE MIXTURES Example 2 A liquid propellant system was prepared employing about 61.7 weight percent of N and 38.3 weight percent of a 50-50 mixture of EDH and hydrazine. The fuel and oxidizer components were fed from separate storage reservoirs into a combustion zone, whereupon contact they spontaneously ignited and readily burned. The calculated specific impulse of the reaction mixture was 290.1 seconds which is substantially the same as exhibited by a N O -hydrazine system itself.
In a manner similar to that described for the foregoing example, a 50-50 weight percent mixture of EDH and UDMH can be employed as a fuel in a bipropellant system with hydrogen peroxide oxidizer. Likewise a ternary mixture of about equal parts by weight of EDH-UDMH- N I-L; can be used as a fuel with a fuming nitric acid oxidant. Again a mixture of 20 weight percent 1,2,3,4- tetrahydrazinobutane and 80 weight percent hydrazine can be employed as a liquid fuel in a bi-propellant system employing liquid oxygen as an oxidizer. Also 1,2,3,4,5,6- hexahydrazinohexane can be admixed with hydrazine to provide a propellant fuel having the desired characteristics set forth herein.
Various modifications can be made in the present invention without deparating from the spirit or scope thereof, for it is to be understood that we limit ourselves only as defined in the appended claims.
We claim:
1. A liquid propellant fuel comprising in combination a hydrazinoalklane and a member selected from the group consisting of hydrazine, mono and dimethyl substituted hydrazines and mixtures thereof, said hydrazinoalkane being a compound corresponding to the general formula LHI INHQJn wherein n is an integer ranging from 2 to about 6, the amount of said hydrazinoalkane in said composition ranging from about 5 percent, based on the total composition weight, up to an amount wherein said composition becomes too viscous for ready handling.
2. In a liquid propellant composition consisting essentially of hydrazine, mono and dimethyl hydrazines and mixtures thereof, the improvement which comprises incorporating into said composition at least 5 weight percent of a hydrazinoalkane freezing point depressant and density increaser corresponding to the general formula Elli l LHI INH 2 n wherein n is an integer ranging from 2 to about 6.
3. A liquid propellant composition comprising from about 5 to about 95 weight percent 1,2-dihydrazinoethane and from about 95 to about 5 percent substantialy anhydrous hydrazine.
4. A liquid propellant composition comprising about weight percent 1,2-dihydrazinoethane and about 50 weight percent substantialy anhydrous hydrazine.
5. A liquid rocket propellant comprising from about 10 to about 40 weight percent uns.-dimethylhydrazine, about 40 to about weight percent hydrazine and about 5 to 50 weight percent 1,2-dihydrazinoethane.
6. A liquid propellant fuel which comprises in about equal weight proportions a ternary mixture of uns.-dimethylhydrazine, hydrazine and 1,2-dihydrazinoethane.
References Cited by the Examiner UNITED STATES PATENTS 2,822,354 2/1958 Uranck et al 260-583 X REUBEN EPSTEIN, Primary Examiner.
CARL D. QUARFORTH, LEON D. ROSDOL,
Examiners.

Claims (1)

1. A LIQUID PROPELLANT FUEL COMPRISING IN COMBINATION A HYDRAZINOALKLANE AND A MEMBER SELECTED FROM THE GROUP CONSISTING OF HYDRAZINE, MONO AND DIMETHYL SUBSTITUTED HYDRAZINES AND MIXTURES THEREOF, SAID HYDRAZINOALKANE BEING A COMPOUND CORRESPONDING TO THE GENERAL FORMULA
US202346A 1962-06-07 1962-06-07 Fuel comprising a hydrazinoalkane and hydrazines Expired - Lifetime US3219500A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US202346A US3219500A (en) 1962-06-07 1962-06-07 Fuel comprising a hydrazinoalkane and hydrazines

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US202346A US3219500A (en) 1962-06-07 1962-06-07 Fuel comprising a hydrazinoalkane and hydrazines

Publications (1)

Publication Number Publication Date
US3219500A true US3219500A (en) 1965-11-23

Family

ID=22749498

Family Applications (1)

Application Number Title Priority Date Filing Date
US202346A Expired - Lifetime US3219500A (en) 1962-06-07 1962-06-07 Fuel comprising a hydrazinoalkane and hydrazines

Country Status (1)

Country Link
US (1) US3219500A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3288660A (en) * 1963-02-11 1966-11-29 Dow Chemical Co Nitrogenous base composition
US4946522A (en) * 1981-06-15 1990-08-07 The United States Of America As Represented By The Secretary Of The Navy Liquid monopropellant for a gun

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2822354A (en) * 1953-03-30 1958-02-04 Phillips Petroleum Co Dihydrazines in aqueous emulsion polymerization

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2822354A (en) * 1953-03-30 1958-02-04 Phillips Petroleum Co Dihydrazines in aqueous emulsion polymerization

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3288660A (en) * 1963-02-11 1966-11-29 Dow Chemical Co Nitrogenous base composition
US4946522A (en) * 1981-06-15 1990-08-07 The United States Of America As Represented By The Secretary Of The Navy Liquid monopropellant for a gun

Similar Documents

Publication Publication Date Title
EP0066999B1 (en) Process for co-nitrating trimethylolethane and diethylene glycol
US3066479A (en) Stabilized azide fuel and combustion process
US3700393A (en) Liquid bipropellant system using aqueous hydroxylammonium perchlorate oxidizer
US3219500A (en) Fuel comprising a hydrazinoalkane and hydrazines
US3088272A (en) Stable propellants
US5837930A (en) Propellants, in particular for the propulsion of vehicles such as rockets, and process for their preparation
US3019081A (en) Stabilized nitric acid
US3342814A (en) Adducts of metal borohydrides and organic polynitrogen compounds
US3018619A (en) Monopropellants containing quaternary ammonium compounds
US3103782A (en) Propellant compositions
US3405130A (en) Adducts of aluminum, beryllium and zirconium borohydrides with nitrogen and/or oxygen-containing ligands
US3664132A (en) Hypergolic propellant systems using tetraformaltrisazine
US3140317A (en) Nitroform-hydrazine coordination compounds
US3213609A (en) High energy propellant and process employing hydrazines and nitro compounds
US2769304A (en) Hypergolic fuel and the method of using it
US3345821A (en) Storable liquid rocket propellants containing tetranitromethane with difluoramino compounds and method of use
US3705495A (en) Fuel systems and oxidizers
US3024595A (en) Method of rocket propulsion using liquid ammonia and ammonium perchlorate
US2771737A (en) Piperidines as hypergolic fuels
US3357185A (en) Operation of reaction motors
US3384674A (en) Stabilization of nitroform salts
US2944385A (en) Stable monopropellants
US3138498A (en) Lithium perchlorate-hydrazine coordination compound and propellant
US3338762A (en) Solid propellant composition with boron containing fuel and nitrogen containing oxidizers
US3730793A (en) Ethyldecaborane or b5h9 with mixed cif5 oxidizer