US3667524A - High-energy propellant containing coated hydrazinium azide - Google Patents

High-energy propellant containing coated hydrazinium azide Download PDF

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US3667524A
US3667524A US828052*A US3667524DA US3667524A US 3667524 A US3667524 A US 3667524A US 3667524D A US3667524D A US 3667524DA US 3667524 A US3667524 A US 3667524A
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hydrazinium azide
globules
hydrazinium
azide
propellant
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John E Paustian
Marvin M Fein
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ATK Launch Systems LLC
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Thiokol Corp
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    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B45/00Compositions or products which are defined by structure or arrangement of component of product
    • C06B45/18Compositions or products which are defined by structure or arrangement of component of product comprising a coated component
    • C06B45/30Compositions or products which are defined by structure or arrangement of component of product comprising a coated component the component base containing an inorganic explosive or an inorganic thermic component
    • C06B45/32Compositions or products which are defined by structure or arrangement of component of product comprising a coated component the component base containing an inorganic explosive or an inorganic thermic component the coating containing an organic compound
    • C06B45/34Compositions or products which are defined by structure or arrangement of component of product comprising a coated component the component base containing an inorganic explosive or an inorganic thermic component the coating containing an organic compound the compound being an organic explosive or an organic thermic component
    • 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

  • This invention relates to a high-energy propellant and more particularly to a propellant that can advantageously be used for propelling projectiles to high velocities.
  • hydrazinium azide has been utilized as a gun propellant in loose powder and pressed pellet forms.
  • hydrazinium azide propellants are not completely satisfactory from the standpoint of control and reproducibility of their burning rates.
  • the burning characteristics of the aforesaid types of hydrazinium azide gun propellants are such that the pressure produced in a gun barrel in which the propellants are used is initially high but rapidly decreases before a projectile propelled thereby reaches the muule of the gun barrel.
  • the barrel pressure produced by hydrazinium azide gun propellants preferably should be relatively constant throughout the travel of a projectile in a gun barrel.
  • previously available hydrazinium azide propellants undergo a considerable decrease in efficacy when they are exposed, even for a relatively short period, to moist environments.
  • Another object of this invention is to provide an efficient method of producing an improved hydrazinium azide product.
  • Still another object of this invention is to provide a hydrazinium azide gun propellant that produces a relatively constant barrel pressure in a gun in which it is employed.
  • An additional object of this invention is to provide a hydrazinium azide product having burning characteristics that make it a more effective gun propellant than known hydrazinium azide gun propellants.
  • a further object of this invention is to provide a hydrazinium azide gun propellant that is less susceptible to deterioration, when exposed to a moist environment, than the hydrazinium azide gun propellants heretofore available.
  • hydrazinium azide propellants in accordance with the present invention are prepared by: (l) melting hydrazinium azide and dropping it into a column of liquid which has a density only slightly less than that of said hydrazinium azide and which has a heated upper stratum and a cooled lower stratum, thereby forming solid globules of the hydrazinium azide; (2) contacting these globules with a solution comprising a non-aqueous vehicle and a coating material having a burning rate lower than that of said hydrazinium azide, so as to thereby cover the surface of each of said globules with the vehicle-coating material solution; and (3) thereafter contacting the solution-covered globules with an extraction liquid in which the non-aqueous vehicle is soluble and in which the coating material is insoluble, so as to thereby transfer the non-aqueous vehicle from the surfaces of the hydrazinium azide globules to the aforesaid extraction liquid while
  • apparatus 10 comprises a vertical, closed tubular column 12 the lower end of which is fixedly attached to, and in communication with the interior 14 of, a frustoconical vessel 16.
  • vessel 16 is open and formed with a circumferentially extending, laterally projecting flange 18 to which is detachably connected a disk-shaped closure member 20.
  • a discharge conduit 22 Fixedly joined to, and depending from, closure member 20 is a discharge conduit 22 the upper end of which communicates with an aperture in said closure member (and thus with the interior 14 of vessel 16 when the closure member is attached to flange 18 as illustrated).
  • Conduit 22 is provided with a valve 30 that can be opened to draw ofi this liquid as desired.
  • a wire screen 31 is positioned over conduit 22 to retain the hydrazinium azide product 32 produced in apparatus 10 and collected in vessel 16.
  • a reflux column 40 extends obliquely from the upper end of column 12 and communicates with the interior of the latter and with a duct 42, this reflux column passing through an aperture 44 formed in the side wall 46 of a closed cylindrical member (generally designated by the number 48) the lower end of which is positioned around the upper portion of column 12. More specifically, member 48 is provided with an apertured partition 50 and with end plates 52, 54 so that its interior is divided into an upper chamber 56 and lower chamber 58, each of said chambers having an inlet 60, 62 and an outlet 64, 66.
  • End plate 52 is formed with a centrally disposed aperture 68 in which a dropping funnel 70 is sealably engaged, this funnel having a lower portion 72 of lesser diameter which extends through the aperture in partition 50, and which is provided with a valve 74 adapted to be actuated from a point outside apparatus 10.
  • the lower portion 72 of dropping funnel 70 also extends through an aperture in the end closure of column 12 to a point below the junction of reflux column 40 with said column 12.
  • Extending laterally from the upper portion of dropping funnel 70 is a charging chute 76 the opening of which can be sealed by a detachable lid 78.
  • a duct 79 communicatively connects duct 42 with the interior 82 of dropping funnel 70.
  • Disposed around reflux column 40 is a heat exchanger 86 having an inlet 88 and an outlet 90.
  • apparatus 10 may be formed of many different well-known materials, such as, for example, glass or suitable metals.
  • column 12 and vessel 16 are filled with 1,2- dichloroethane, the surface level of this liquid being maintained at a point above the end of portion 72 of dropping funnel 70 and below the junction of reflux column 40 with column 12.
  • valve 74 closed, solid hydrazinium azide is charged into the larger upper portion of dropping funnel 70 through chute 76 and the dropping funnel is sealed by securing lid 78 to the top of said chute.
  • a suitable hot liquid is then pumped through inlet 60 into the annular space between dropping funnel 70 and member 48 and out through outlet 64.
  • an inert gas such as nitrogen is forced, substantially at atmospheric pressure, through duct 42 in the direction indicated by the arrow in the drawing.
  • the temperature of the hot liquid injected into inlet 60 is slightly higher than the melting point of hydrazinium azide, or above about 75 C.
  • a suitable hot liquid is also pumped through inlet 62 into the annular space between the upper end of column 12 and member 48 and out through outlet 66 (the temperature of this liquid preferably being such that the upper stratum of the 1,2-dichloroethane in column 12 is maintained at about C. and a suitable coolant is pumped through inlet 36 into the annular space between the lower end of column 12 and the wall of heat exchanger 34 and out through outlet 38 (the temperature of this coolant being such that the 1,2- dichloroethane in the lower portion of column 14 is maintained at a temperature of about 1S C. to about -l0 C.).
  • the temperature of the upper end of reflux column 40 is maintained at about 15 C. by pumping a suitable coolant through heat exchanger 86.
  • valve 74 is opened to permit dropwise flow of the hot hydrazinium azide through the orifice in the lower portion 72 of said dropping funnel and into the heated upper stratum of the l,2-dichloroethane in column 12. Because the density (L25 gm/cc) of l,2-dichloroethane is only slightly less than that (1.38 gm/cc) of hydrazinium azide, each drop of the latter settles slowly toward vessel 16 and is gradually cooled. After passing through the stratum of the 1,2-dichloroethane which is at a temperature of about 15 C. to about l C., each drop of hydrazinium azide is solidified into a spherical solid particle.
  • inert gas forced through duct 42 not only enters the space above the hydrazinium azide in dropping funnel 70 but also enters reflux column 40.
  • the design of apparatus minimizes the possibility of ignition of any combustible vapors in dropping funnel 70, reflux column 40 and the upper end of column 12.
  • the dimensions of certain components of apparatus 10 will vary depending upon the size of the globules of hydrazinium azide that it is desired to produce.
  • the diameter of the orifice in the lower portion 72 of dropping funnel 70 may be made relatively large in order to introduce large drops of the melted hydrazinium azide into the l,2-dichloroethane in column 12, and to thereby produce a product in the form of relatively large globules.
  • smaller globules of hydrazinium azide can be formed by use of a small orifice in the lower portion of dropping funnel 70.
  • valve 30 in discharge conduit 22 is opened to drain the l,2-dichloroethane from said vessel and column 12.
  • Closure member is then detached from vessel 16 and the hydrazinium azide globules are screened to separate them into different size ranges.
  • the hydrazinium azide globules obtained by the above-described process and apparatus can be dried by conventional techniques and then utilized as a high-energy gun propellant for hypervelocity applications.
  • the globules of a selected size range are preferably coated with a coating material that will modify the burning characteristics of the globules and also protect them from moisture absorption.
  • This coating preferably is applied to the globules by mixing them with a solution consisting of: (1) about 1 to 10 percent by weight of a coating material, preferably nitrocellulose, which has a burning rate lower than that of hydrazinium azide and which will also protect said hydrazinium azide from moisture absorption; and (2) a nonaqueous vehicle, preferably ethyl acetate, which is soluble (or miscible) with a second liquid that will be described hereinafter.
  • the hydrazinium azide globules can readily be coated with the aforedescribed non-aqueous vehicle-coating material solution by mixing the materials in a suitable vessel, it will be obvious that other means can be employed to cover the globules with this solution, such as, for example, conventional spraying apparatus. It has been found preferable to mix the hydrazinium azide globules with a lacquer consisting of about 2.5 percent by weight nitrocellulose and about 97.5 percent by weight of ethyl acetate, mixing being effected at atmospheric temperature and pressure in a conventional blending machine and with a ratio of 1 gm. of hydrazinium azide globules per 2.5 ml.
  • the resulting slurry is mixed with an extraction liquid in which the non-aqueous vehicle is soluble and in which the selected coating material is insoluble.
  • slurry of hydrazinium azide globules and nitrocellulose-ethyl acetate solution is slowly added to a liquid consisting of about 75 percent by volume of l,2-dichloroethane and 25 percent by volume of carbon tetrachloride, and this mixture is agitated for approximately 15 minutes at atmospheric pressure and temperature, which transfers the ethyl-acetate (the nonaqueous vehicle" used in the preferred process) from the surfaces of the hydrazinium azide globules while leaving the nitrocellulose (the coating material" used in the preferred process) on the surfaces of said globules.
  • a liquid consisting of about 75 percent by volume of l,2-dichloroethane and 25 percent by volume of carbon tetrachloride
  • the slurry of hydrazinium azide globules and nitrocellulose-ethyl acetate solution is combined with the mixture of l,2-dichloroethane and carbon tetrachloride in the ratio of 6.25 ml. of the latter per each gram of hydrazinium azide globules in the slurry.
  • the l,2-dichloroethane-carbon tetrachloride mixture is particularly advantageous as the extraction liquid because of its miscibility with ethyl acetate, its non-flammability, and the insolubility of both hydrazinium azide and nitrocellulose in said mixture.
  • the density of the mixture of the slurry and extraction liquid is such that the hydrazinium azide globules coated with the nitrocellulose-ethyl acetate lacquer are suspended in the mixture, whereas the globules which are coated only with nitrocellulose (i.e., the globules from whose lacquer-covered surfaces the ethyl acetate has been extracted) sink, thereby minimizing agglomeration of the nitrocellulose-coated globules and lacquer-coated globules. Agitation of the mixture is continued until the ethyl acetate in the lacquer on the hydrazinium azide globules has been completely extracted.
  • the globules are dried by exposing them to a stream of dry air at a temperature of 40 C.
  • a particular advantage of the disclosed process for preparing hydrazinium azide propellant is that the hydrazinium azide particles produced thereby are uniformly spherical in shape, which simplifies the preparation of a propellant having controlled, reproducible and uniform burning characteristics.
  • the disclosed process can also readily be adapted to produce hydrazinium azide globules of different sizes, which can be selectively blended to provide propellants of different burning characteristics.
  • the nitrocellulose-coated globular hydrazinium azide propellant of this invention is particularly advantageous as a gun propellant as it produces a relatively constant pressure in a gun barrel throughout the travel of the projectile therein. Furthermore, the nitrocellulose coating on each hydrazinium azide globule is uniformly applied by the coating process herein disclosed and serves to protect the hydrazinium azide 6 from moisture absorption.
  • the scope of this invention is not 1. a propellant consisting of hydrazinium azide in the form limited, however, globular hydrazinil-lm alide propellant of substantially spherical solid particles, said particles being that is coated, or to the same propellant coated with nitrocelted ith a non-hy rosco ic coating material.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

A high energy propellant of hydrazinium azide coated with a nonhygroscopic coating.

Description

United States Patent Paustian et al.
[451 June 6,1972
HIGH-ENERGY PROPELLANT CONTAINING COATED HYDRAZINIUM AZIDE Inventors: John E. Paustian, Whippany; Marvin M.
Fein, Westfield, both of NJ.
Assignee: Thiokol Chemical Corporation, Bristol, Pa.
Filed: Mar. 28, 1969 Appl. No.: 828,052
Related US. Application Data Division of Ser. No. 551,838, May 12, 1966, Pat. No. 3,459,607. 7
US. Cl ..149/8, 149/5, 149/94,
149/96, 149/100 Int. Cl. ..C06b 19/02 Field of Search ..1 17/100; 149/2, 5, 6, 7, 36,
Paustian et a1 149/36 lim ry Ex m ne 1 yl. Qy t Assisla t Examiner-Stephen J. Lechert, Jr. Attorney-Thomas W. Brennan ABSTRACT A high energy propellant of hydrazinium azide coated with a non-hygroscopic coating.
3 Claims, 1 Drawing Figure PATENTEDJUN s :972
INERT GAS INVENTORS JOHN E. PAUsr/A/v MARVIN M FE/N HIGH-ENERGY PROPELLANT CONTAINING COATED HYDRAZINIUM AZIDE This application is a division of Application Ser. No. 551,838, filed May 12, 1966 now U.S. Pat. No. 3,459,607 issued on Aug. 5, I969.
This invention relates to a high-energy propellant and more particularly to a propellant that can advantageously be used for propelling projectiles to high velocities.
Heretofore, hydrazinium azide has been utilized as a gun propellant in loose powder and pressed pellet forms. In such forms, however, hydrazinium azide propellants are not completely satisfactory from the standpoint of control and reproducibility of their burning rates. Furthermore, the burning characteristics of the aforesaid types of hydrazinium azide gun propellants are such that the pressure produced in a gun barrel in which the propellants are used is initially high but rapidly decreases before a projectile propelled thereby reaches the muule of the gun barrel. As will be understood by persons skilled in the art of gun propellants, the barrel pressure produced by hydrazinium azide gun propellants preferably should be relatively constant throughout the travel of a projectile in a gun barrel. In addition, previously available hydrazinium azide propellants undergo a considerable decrease in efficacy when they are exposed, even for a relatively short period, to moist environments.
It is accordingly a broad object of this invention to provide an improved hydrazinium azide product which can advantageously be used as a gun propellant, as well as for other purposes.
Another object of this invention is to provide an efficient method of producing an improved hydrazinium azide product.
Still another object of this invention is to provide a hydrazinium azide gun propellant that produces a relatively constant barrel pressure in a gun in which it is employed.
An additional object of this invention is to provide a hydrazinium azide product having burning characteristics that make it a more effective gun propellant than known hydrazinium azide gun propellants.
A further object of this invention is to provide a hydrazinium azide gun propellant that is less susceptible to deterioration, when exposed to a moist environment, than the hydrazinium azide gun propellants heretofore available.
Briefly described, hydrazinium azide propellants in accordance with the present invention are prepared by: (l) melting hydrazinium azide and dropping it into a column of liquid which has a density only slightly less than that of said hydrazinium azide and which has a heated upper stratum and a cooled lower stratum, thereby forming solid globules of the hydrazinium azide; (2) contacting these globules with a solution comprising a non-aqueous vehicle and a coating material having a burning rate lower than that of said hydrazinium azide, so as to thereby cover the surface of each of said globules with the vehicle-coating material solution; and (3) thereafter contacting the solution-covered globules with an extraction liquid in which the non-aqueous vehicle is soluble and in which the coating material is insoluble, so as to thereby transfer the non-aqueous vehicle from the surfaces of the hydrazinium azide globules to the aforesaid extraction liquid while leaving the coating material on said globules.
The novel features of the present invention, as well as additional objects and advantages thereof, will be more clearly understood from the following description, in which reference is made to the accompanying schematic representation of apparatus that can advantageously be used in producing hydrazinium azide propellant in accordance with the invention.
Throughout the specification and drawing, the same numbers designate the same or corresponding parts.
In the accompanying drawing the number generally designates one apparatus that can be employed in carrying out a process embodiment of this invention. More particularly, apparatus 10 comprises a vertical, closed tubular column 12 the lower end of which is fixedly attached to, and in communication with the interior 14 of, a frustoconical vessel 16. The
lower end of vessel 16 is open and formed with a circumferentially extending, laterally projecting flange 18 to which is detachably connected a disk-shaped closure member 20. Fixedly joined to, and depending from, closure member 20 is a discharge conduit 22 the upper end of which communicates with an aperture in said closure member (and thus with the interior 14 of vessel 16 when the closure member is attached to flange 18 as illustrated). Connected to vessel 16 is a conduit 24 in which there is a valve 26 that can be opened to till the vessel and column 12 with a liquid 28 to be described hereinafter. Conduit 22 is provided with a valve 30 that can be opened to draw ofi this liquid as desired. A wire screen 31 is positioned over conduit 22 to retain the hydrazinium azide product 32 produced in apparatus 10 and collected in vessel 16.
Disposed around the lower portion of column 12 is a heat exchanger 34 having an inlet 36 and outlet 38. A reflux column 40 extends obliquely from the upper end of column 12 and communicates with the interior of the latter and with a duct 42, this reflux column passing through an aperture 44 formed in the side wall 46 of a closed cylindrical member (generally designated by the number 48) the lower end of which is positioned around the upper portion of column 12. More specifically, member 48 is provided with an apertured partition 50 and with end plates 52, 54 so that its interior is divided into an upper chamber 56 and lower chamber 58, each of said chambers having an inlet 60, 62 and an outlet 64, 66. End plate 52 is formed with a centrally disposed aperture 68 in which a dropping funnel 70 is sealably engaged, this funnel having a lower portion 72 of lesser diameter which extends through the aperture in partition 50, and which is provided with a valve 74 adapted to be actuated from a point outside apparatus 10. The lower portion 72 of dropping funnel 70 also extends through an aperture in the end closure of column 12 to a point below the junction of reflux column 40 with said column 12. Extending laterally from the upper portion of dropping funnel 70 is a charging chute 76 the opening of which can be sealed by a detachable lid 78. A duct 79 communicatively connects duct 42 with the interior 82 of dropping funnel 70. Disposed around reflux column 40 is a heat exchanger 86 having an inlet 88 and an outlet 90.
It will be recognized that the above-described components of apparatus 10 may be formed of many different well-known materials, such as, for example, glass or suitable metals.
In accordance with a preferred method embodiment of this invention, column 12 and vessel 16 are filled with 1,2- dichloroethane, the surface level of this liquid being maintained at a point above the end of portion 72 of dropping funnel 70 and below the junction of reflux column 40 with column 12. With valve 74 closed, solid hydrazinium azide is charged into the larger upper portion of dropping funnel 70 through chute 76 and the dropping funnel is sealed by securing lid 78 to the top of said chute. A suitable hot liquid is then pumped through inlet 60 into the annular space between dropping funnel 70 and member 48 and out through outlet 64. Simultaneously an inert gas such as nitrogen is forced, substantially at atmospheric pressure, through duct 42 in the direction indicated by the arrow in the drawing. The temperature of the hot liquid injected into inlet 60 is slightly higher than the melting point of hydrazinium azide, or above about 75 C. A suitable hot liquid is also pumped through inlet 62 into the annular space between the upper end of column 12 and member 48 and out through outlet 66 (the temperature of this liquid preferably being such that the upper stratum of the 1,2-dichloroethane in column 12 is maintained at about C. and a suitable coolant is pumped through inlet 36 into the annular space between the lower end of column 12 and the wall of heat exchanger 34 and out through outlet 38 (the temperature of this coolant being such that the 1,2- dichloroethane in the lower portion of column 14 is maintained at a temperature of about 1S C. to about -l0 C.). The temperature of the upper end of reflux column 40 is maintained at about 15 C. by pumping a suitable coolant through heat exchanger 86.
After the hydrazinium azide in dropping funnel 70 has been melted, valve 74 is opened to permit dropwise flow of the hot hydrazinium azide through the orifice in the lower portion 72 of said dropping funnel and into the heated upper stratum of the l,2-dichloroethane in column 12. Because the density (L25 gm/cc) of l,2-dichloroethane is only slightly less than that (1.38 gm/cc) of hydrazinium azide, each drop of the latter settles slowly toward vessel 16 and is gradually cooled. After passing through the stratum of the 1,2-dichloroethane which is at a temperature of about 15 C. to about l C., each drop of hydrazinium azide is solidified into a spherical solid particle.
It will be noted that the inert gas forced through duct 42 not only enters the space above the hydrazinium azide in dropping funnel 70 but also enters reflux column 40. Thus the design of apparatus minimizes the possibility of ignition of any combustible vapors in dropping funnel 70, reflux column 40 and the upper end of column 12.
The dimensions of certain components of apparatus 10 will vary depending upon the size of the globules of hydrazinium azide that it is desired to produce. For example, the diameter of the orifice in the lower portion 72 of dropping funnel 70 may be made relatively large in order to introduce large drops of the melted hydrazinium azide into the l,2-dichloroethane in column 12, and to thereby produce a product in the form of relatively large globules. Conversely, smaller globules of hydrazinium azide can be formed by use of a small orifice in the lower portion of dropping funnel 70. It has been found that well-formed globules having a diameter between about 0.075 inch and 0.125 inch are produced in apparatus of the type described and illustrated, wherein the diameter of the orifice in the lower portion 72 of dropping funnel is 0.023 inch and the distance between the end of said portion 72 and the bottom of vessel 16 is in the range of about l8-24 inches.
After a quantity of hydrazinium azide globules has been collected in vessel 16 the valve 30 in discharge conduit 22 is opened to drain the l,2-dichloroethane from said vessel and column 12. Closure member is then detached from vessel 16 and the hydrazinium azide globules are screened to separate them into different size ranges. The hydrazinium azide globules obtained by the above-described process and apparatus can be dried by conventional techniques and then utilized as a high-energy gun propellant for hypervelocity applications. However, in accordance with the principles of this invention, the globules of a selected size range (which will vary according to the intended use of the propellant) are preferably coated with a coating material that will modify the burning characteristics of the globules and also protect them from moisture absorption. This coating preferably is applied to the globules by mixing them with a solution consisting of: (1) about 1 to 10 percent by weight of a coating material, preferably nitrocellulose, which has a burning rate lower than that of hydrazinium azide and which will also protect said hydrazinium azide from moisture absorption; and (2) a nonaqueous vehicle, preferably ethyl acetate, which is soluble (or miscible) with a second liquid that will be described hereinafter. Although the hydrazinium azide globules can readily be coated with the aforedescribed non-aqueous vehicle-coating material solution by mixing the materials in a suitable vessel, it will be obvious that other means can be employed to cover the globules with this solution, such as, for example, conventional spraying apparatus. It has been found preferable to mix the hydrazinium azide globules with a lacquer consisting of about 2.5 percent by weight nitrocellulose and about 97.5 percent by weight of ethyl acetate, mixing being effected at atmospheric temperature and pressure in a conventional blending machine and with a ratio of 1 gm. of hydrazinium azide globules per 2.5 ml. of the nitrocelluloseethyl acetate solution. After the globules have been thoroughly mixed with a selected non-aqueous vehicle-coating material solution, the resulting slurry is mixed with an extraction liquid in which the non-aqueous vehicle is soluble and in which the selected coating material is insoluble. In the preferred embodiment of the invention herein described, the
slurry of hydrazinium azide globules and nitrocellulose-ethyl acetate solution is slowly added to a liquid consisting of about 75 percent by volume of l,2-dichloroethane and 25 percent by volume of carbon tetrachloride, and this mixture is agitated for approximately 15 minutes at atmospheric pressure and temperature, which transfers the ethyl-acetate (the nonaqueous vehicle" used in the preferred process) from the surfaces of the hydrazinium azide globules while leaving the nitrocellulose (the coating material" used in the preferred process) on the surfaces of said globules. The slurry of hydrazinium azide globules and nitrocellulose-ethyl acetate solution is combined with the mixture of l,2-dichloroethane and carbon tetrachloride in the ratio of 6.25 ml. of the latter per each gram of hydrazinium azide globules in the slurry. The l,2-dichloroethane-carbon tetrachloride mixture is particularly advantageous as the extraction liquid because of its miscibility with ethyl acetate, its non-flammability, and the insolubility of both hydrazinium azide and nitrocellulose in said mixture. Also the density of the mixture of the slurry and extraction liquid is such that the hydrazinium azide globules coated with the nitrocellulose-ethyl acetate lacquer are suspended in the mixture, whereas the globules which are coated only with nitrocellulose (i.e., the globules from whose lacquer-covered surfaces the ethyl acetate has been extracted) sink, thereby minimizing agglomeration of the nitrocellulose-coated globules and lacquer-coated globules. Agitation of the mixture is continued until the ethyl acetate in the lacquer on the hydrazinium azide globules has been completely extracted.
After the nitrocellulose-coated globules of hydrazinium azide have been separated from the aforedescribed mixture of extraction liquid and non-aqueous vehicle (which can be accomplished by simply pouring off the liquid), the globules are dried by exposing them to a stream of dry air at a temperature of 40 C.
The utility of both the uncoated and nitrocellulose-coated globular hydrazinium azide propellant disclosed herein is demonstrated by the ballistic data presented in the following table, which were obtained by utilizing the two forms of the propellant in a caliber 0.300 Weatherby Magnum cartridge with a 4.3 grain spherical projectile formed of a polymeric material.
Propellant Peak Propellant Weight Barrel Muzzle (Grains) Pressure Velocity Hydrazinium azide globules (uncoated, size range 0.075-0.l25 inch) 45.1 20,500 6531 56.3 52,000 7977 62.1 60,600 8419 67.5 73,500 8792 Hydrazinium azide globules (nitrocellulose-coated, size range 0.0750.l25 inch) 60.0 69,200 8531 A particular advantage of the disclosed process for preparing hydrazinium azide propellant is that the hydrazinium azide particles produced thereby are uniformly spherical in shape, which simplifies the preparation of a propellant having controlled, reproducible and uniform burning characteristics. The disclosed process can also readily be adapted to produce hydrazinium azide globules of different sizes, which can be selectively blended to provide propellants of different burning characteristics.
The nitrocellulose-coated globular hydrazinium azide propellant of this invention is particularly advantageous as a gun propellant as it produces a relatively constant pressure in a gun barrel throughout the travel of the projectile therein. Furthermore, the nitrocellulose coating on each hydrazinium azide globule is uniformly applied by the coating process herein disclosed and serves to protect the hydrazinium azide 6 from moisture absorption. The scope of this invention is not 1. a propellant consisting of hydrazinium azide in the form limited, however, globular hydrazinil-lm alide propellant of substantially spherical solid particles, said particles being that is coated, or to the same propellant coated with nitrocelted ith a non-hy rosco ic coating material. lulose. It will be apparent to those skilled in the art that other 2 The propellant f claim 1 wherein the coating material embodiments, as well as modifications to those disclosed, can 5 has a burning rate lower than that ofsaid hydrazinium an-de be made and practiced without departing from the scope of the invention, for the limits of which reference must be made f r of l wherem sad coaung material to the appended claims. mtmce What is claimed is:

Claims (2)

  1. 2. The propellant of claim 1 wherein the coating material has a burning rate lower than that of said hydrazinium azide.
  2. 3. The propellant of claim 1 wherein said coating material is nitrocellulose.
US828052*A 1966-05-12 1969-03-28 High-energy propellant containing coated hydrazinium azide Expired - Lifetime US3667524A (en)

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US82805269A 1969-03-28 1969-03-28

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4390380A (en) * 1980-03-31 1983-06-28 Camp Albert T Coated azide gas generating composition
US6345577B1 (en) 2000-09-27 2002-02-12 The United States Of America As Represented By The Secretary Of The Navy Energetic deterrent coating for gun propellant
US6443502B1 (en) 1999-04-22 2002-09-03 Denso Corporation Leakage restriction device for refrigeration cycle

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3222231A (en) * 1962-09-18 1965-12-07 Atlantic Res Corp Process for producing finely divided rounded particles
US3288659A (en) * 1962-01-24 1966-11-29 Dow Chemical Co Metallized rocket propellants containing azides
US3309248A (en) * 1962-01-24 1967-03-14 Dow Chemical Co Solid propellants containing hydrazonium azide and boron compounds
US3419443A (en) * 1967-04-17 1968-12-31 Explosives Corp America Hydrazine containing explosive compositions
US3459607A (en) * 1966-05-12 1969-08-05 Thiokol Chemical Corp High-energy propellant

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3288659A (en) * 1962-01-24 1966-11-29 Dow Chemical Co Metallized rocket propellants containing azides
US3309248A (en) * 1962-01-24 1967-03-14 Dow Chemical Co Solid propellants containing hydrazonium azide and boron compounds
US3222231A (en) * 1962-09-18 1965-12-07 Atlantic Res Corp Process for producing finely divided rounded particles
US3459607A (en) * 1966-05-12 1969-08-05 Thiokol Chemical Corp High-energy propellant
US3419443A (en) * 1967-04-17 1968-12-31 Explosives Corp America Hydrazine containing explosive compositions

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4390380A (en) * 1980-03-31 1983-06-28 Camp Albert T Coated azide gas generating composition
US6443502B1 (en) 1999-04-22 2002-09-03 Denso Corporation Leakage restriction device for refrigeration cycle
US6345577B1 (en) 2000-09-27 2002-02-12 The United States Of America As Represented By The Secretary Of The Navy Energetic deterrent coating for gun propellant

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