US2916775A - Propellent powder - Google Patents

Propellent powder Download PDF

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US2916775A
US2916775A US220533A US22053351A US2916775A US 2916775 A US2916775 A US 2916775A US 220533 A US220533 A US 220533A US 22053351 A US22053351 A US 22053351A US 2916775 A US2916775 A US 2916775A
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nitrocellulose
solvent
propellant
powder
temperature
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US220533A
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Jr John J O'neill
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Olin Corp
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Olin Corp
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    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B21/00Apparatus or methods for working-up explosives, e.g. forming, cutting, drying
    • C06B21/0033Shaping the mixture
    • C06B21/0066Shaping the mixture by granulation, e.g. flaking
    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B21/00Apparatus or methods for working-up explosives, e.g. forming, cutting, drying
    • C06B21/0008Compounding the ingredient
    • C06B21/0025Compounding the ingredient the ingredient being a polymer bonded explosive or thermic component
    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B21/00Apparatus or methods for working-up explosives, e.g. forming, cutting, drying
    • C06B21/0033Shaping the mixture
    • C06B21/0058Shaping the mixture by casting a curable composition, e.g. of the plastisol type

Definitions

  • This invention relates to the manufacture of propellent explosives and more particularly to the production of rocket powder.
  • Giant grains of propellant suitable for use as rocket powder by the military or for use as jet-assisted takeoff rockets for aircraft ordinarily have a grain diameter of from one to several inches and lengths sometimes over one foot or more.
  • Herctofore, such large grains have been prepared by extruding the explosive composition which had previously been prepared in gelatinized sheet form. The production of such sheets has required a series of rolling operations, removal of volatile matter being accomplished during the final rolling steps, or by a subsequent drying treatment. Gelatinization was effected by the rolling, frequently supplemented by intermediate kneadirig operations, with the 'rolls ordinarily being heated. The resulting sheet or carpet of explosives was then rolled into a bundle to be inserted in the extruding die.
  • the present invention has as an object the provision of a simplified and improved process for manufacturing rocket powder grains whereby the aforementioned and other disadvantages of prior procedures are overcome.
  • Another object of this invention is to provide a process for producing rocket powder grains of either single or double base composition in which the use of extrusion, rolling, and other pressure methods and devices are eliminated.
  • a further object is to provide an improved casting process for making rocket powder grains of any desired configuration or design.
  • plastisol solvent as used herein is meant a relatively non-volatile liquid which is a slow acting solvent or one having only little or no solvent power for the spherical particles of propellant at low or ordinary room temperatures, but being rapidly acting and having a relatively great solvent power therefor at elevated temperatures.
  • the particles of propellant are advantageously formed by agitating nitrocellulose and a solvent therefor, such as ethyl acetate, with an excess of anon-solvent, such as water, in the presence of a protective colloid, removing the solvent, and thereafter drying the resulting spherical pellets of nitrocellulose.
  • a solvent therefor such as ethyl acetate
  • anon-solvent such as water
  • This surface characteristic is undoubtedly the result of a skin effect occasioned by surface tension and removal of the solvent in the formation of the spheres.
  • Other ingredi ents such as dioctyl phthalate, lead stearate, red lead, centralite, carbon black, dinitrotoluene, and the like, may be incorporated with the nitrocellulose in the formation of the spherical pellets to obtain particular ballistic properties as desired.
  • a relatively free-flowing paste is obtained in'accordance with this invention
  • the spheres are mixed with the proper proportion of the plastisol solvent, whereas if irregular shaped particles, such as may be obtained by merely grinding cannon powder or the like, are utilized, the desirable free-flowing characteristics of the paste are not obtained.
  • the spheres of propellant may be of any desired size, large diameter spheres require relatively longer periods of time in order to effect their solution and resultant solidification of the grain, whereas with smaller spheres, the time is correspondingly reduced.
  • spheres having a diameter not greater than about 0.005 inch and preferably of much'smaller diameter, such as 0.001 inch or less.
  • the ordinary liquid deterrents are generally solvents for nitrocellulose and are admirably suited as the plastisol solvent in the present process, it only being necessary that such deterrent have relatively poor solvent power for the propellant at ordinary room or low temperatures. In other words, the solvent power of such solvent should be insufficient to effect any substantial solution of the propellant at ordinary temperatures during the time required for uniformly mixing the solvent and propellant together and shaping the resultant mixture.
  • energizing modifiers such as nitroglycerine, butane triol trinitrate, diglycol dinitrate, ethylene glycol dinitrate, and the like
  • one or more miscible deterrents such as dibutyl phthalate, dimethyl sebacate, dibutyl succinate, dibutyl adipate, triacetin, ethyl diphenyl phosphate, tributyl phosphate, and the like, to provide plastisol solvents admirably suited for the purpose.
  • the energizing modifier may be omitted from the composition and the plastisol solvent will be composed only of a liquid deterrent, such as one of those set forth above or mixtures of them. 1
  • deterrents suitable therefor at temperatures above their 'melting points are dirnethyl phthalate, dioctyl sebacate, ortho nitro biphenyl, butyl benzyl phthalate, i octyl diphenyl phosphate, triethylene glycol di2-.ethyl butyrate (i.e. 'triglycol-dihexoate), and the like.
  • the amount of plastisol solvent should be such that of the volume of a it forms at least about 25% Substanmixture of the solvent and the propellant.
  • plastisol solvent tends toresult in voids or air pockets in the resulting rocket grain and the mixture with such lesser amounts is generally not sufliciently fluid for the purpose.
  • Greater amounts of plastisol solvent may be utilized to good advantage to increase the fluidity of the mixture, vary the ballistic properties of the resulting rocket grain as desired, and insure absence of voids or air spaces in the grains, but
  • the amount-utilized should preferably not be sufficicntly great to result in segregation'or settling out of the pro pellant during the period required to cause the mixture to set up.
  • the plastlsol solvent is. preferably desiccated or otherwise treated to reduce any traces of moisture to a minimum, and'both the-propellant-and plastisol solment of air and give the desired design of rocket powder grain.
  • Such precautions as desiccating and evacuating are preferably observed in order to minimize the possi-. bility of undesirable voids in the resulting rocket powder grain.
  • heat is applied to elevate the temperature of the. mixture to a temperature preferably in the range of; about 1 58 C. to 90 C. and such temperature is maintained for a timesuiiicient to cause solution of the propellant and setting-up of the mixture, at which time 'the'temperature may be reduced.
  • the higher the temperature used during this treatment the shorter the period required in order to cause the grain to satisfactorily set up or harden, but precaution should be observed not to exceed the combustion or explosive temperature of the mixture.
  • Grains so formed are of uni form composition throughout, may be of any desired design or configuration, and all pressure extrusion steps and undesirable casting techniques are avoided.
  • nitrocellulose having a nitrogen content of about 12.6% are agitated with 4100 parts of water at about 50 C. to form an aqueous slurry.
  • a suspension of carbon black in ethyl acetate is separately prepared by first thoroughly mixing 0.705 part of carbon black with 100 parts of ethyl acetate. This mixture of carbon black and ethyl acetate is then added to 1250 parts more of ethyl acetate, and the resultant dilute carbon black-ethyl acetate mixture is agitated to insure uniform distribution of the suspended particles of carbon black.
  • anemulsi-fying agent such as the water soluble salts of fatty acids, sulphonated oils, the so-called water-soluble oils, and the like, greatly facilitates the formation of small particles of the nitrocellulose solution, and for this reason, twentyfour parts of a 40% aqueous solution of the sodium sulphate derivative of Z-ethylhexanol is added to the bath. One hundred twenty-five parts of sodium sulfate dissolved in 300 parts of water is added over a one hour period and agitation continued for anadditional three hours.
  • the globules are then hardened to form powder ,grains'by removal of the ethyl acetate during continuous agitation and heating up toabout 99 C. in accordance with the practice set forth in US. Patent 2,027,114 re ferred to, hereinbefore.
  • the resultant spherical pellets of propellant are then air dried at 50 C. and are composed of about 87.7% nitrocellulose, 11.0% 'dinitrotoluene, 0.3% carbon black, and 1.0% ethyl centralite and have an average diameter-of-about 0.001 inch, more or less, depending on the degree of agitation used in the formation thereof.
  • a substantially anhydrous plastisol solvent composed of 74% by Weight nitroglycerine, 25% by weight dimethyl phthal-' ate and 1% by weight ethyl centralite, is placed in a vessel and the vessel evacuated to an absolute pressure of about 10 millimeters of mercury and'so maintained i for about sixteen hours.
  • the solvent is then added to After the solvent and, propellant are uniformly mixed,
  • the mixture is then shaped by carefully pouring to avoid entrapmentof air into a mold formed of nitroglycerineresistant plastic such as cellulose acetate, methyl methacrylate, or ethyl cellulose.
  • a mold formed of nitroglycerineresistant plastic such as cellulose acetate, methyl methacrylate, or ethyl cellulose.
  • the percent by volume of plastisol solvent in the mixture is about 41.3%.
  • the mold containing the mixture of solvent and propellant is then placed is an oven, heated to about 75 C. and maintained at this temperature until the propellant is substantially dissolved by the solvent and the grain has set up. This solution and setting up of the grain is readily accomplished in a relatively short time, but for instance, may be conveniently let set over night.
  • Rocket powder grains prepared in accordance with the foregoing example are substantially free of undesirable voids, are substantially uniform in composition throughout the grain, and have the strength and other physical properties requisite for rocket powder grains. It will be apparent that the method is relatively simple lending itself to mass production and that no costly apparatus such as is needed for developing high pressures is needed. It will likewise be apparent that the propellant and plastisol solvent may vary appreciably in composition and that rocket powder grains having substantially any desired ballistic characteristics can be prepared in accordance with this invention. While the foregoing embodiment has been set forth in considerable detail, it is to be distinctly understood that many modifications and variations will naturally present themselves to those skilled in the art without departing from the spirit of this invention or the scope of the appended claims.
  • the method which comprises preparing a substantially uniform pourable paste by mixing together particles of gelatinized nitrocellulose propellant and a liquid plasticizer for the nitrocellulose in the amount of at least about 25% by volume of the resulting mixture and at a temperature at which substantially no dissolution of the nitrocellulose particles in the plasticizers takes place and thereafter maintaining said composition at atmospheric pressure, and at a temperature at which the nitrocellulose will dissolve, until the nitrocellulose is completely dissolved and the resulting substantially homogeneous mass has solidified into a powder grain.
  • the method for making substantially homogeneous and substantially non-porous propellent grains which comprises preparing a pourable paste having a'substantially uniform composition by mixing together pellets of gelatinized nitrocellulose propellant and a liquid plasticizer for nitrocellulose in the amount of at least about 25 percent by volume of the resulting mixture and at a tem.
  • the improved method for making propellent powder grains having a substantially homogeneous nonporous composition which comprises preparing a pourable paste of substantially uniform composition by agitating together pellets of gelatinized nitrocellulose propellant and a liquid plasticizer for nitrocellulose in the amount of at least about 25 percent by volume of the resulting mixture and at a temperature at which substantially no dissolution of the pellets in the plasticizer takes place during said agitation, said plasticizer including in its composition an energizing modifier of the resulting propellent grain, shaping said paste in a suitable mold, and, thereafter, maintaining said paste in said mold at atmospheric pressure and at a temperature at which the nitrocellulose will dissolve until the nitrocellulose has completely dissolved in said plasticizer and the substantially homogeneous mass has solidified into a propellent powder grain having dimensions'and shape conforming substantially to those of said mold.
  • the improved method for making propellent powder grains having a substantially homogeneous nonporous composition which comprises preparing a pourable paste of substantially uniform composition by agitating together pellets of gelatinized nitrocellulose propellant and a liquid plasticizer for nitrocellulose in the amount of at least about 25 by volume of the resulting mixture and at a temperature at which substantially no dissolution of the pellets in the plasticizer takes place during said agitation, shaping said paste in a suitable mold, and, thereafter, heating said paste in said mold at atmospheric pressure and to a temperature at which the nitrocellulose will dissolve until the nitrocellulose has completely dissolved in said plasticizer and the substantially homogeneous mass has solidified into a propellent powder grain having dimensions and shape conforming substantially to those of said mold.

Description

United States Patent-O PROPELLENT POWDER No Drawing. Application April 11, 1951 Serial No. 220,533
4 Claims. 01. 18-55 This invention relates to the manufacture of propellent explosives and more particularly to the production of rocket powder.
Giant grains of propellant suitable for use as rocket powder by the military or for use as jet-assisted takeoff rockets for aircraft ordinarily have a grain diameter of from one to several inches and lengths sometimes over one foot or more. Herctofore, such large grains have been prepared by extruding the explosive composition which had previously been prepared in gelatinized sheet form. The production of such sheets has required a series of rolling operations, removal of volatile matter being accomplished during the final rolling steps, or by a subsequent drying treatment. Gelatinization was effected by the rolling, frequently supplemented by intermediate kneadirig operations, with the 'rolls ordinarily being heated. The resulting sheet or carpet of explosives was then rolled into a bundle to be inserted in the extruding die.
Such a process has the disadvantage that huge presses, rolls, and other explosive equipment capable of producing extremely high pressures are required, and the operation is, at best, very slow and hazardous, requiring many precautions to avoid explosion during extrusion. Furthermore, when the composition contains nitroglycerine, considerable nitroglycerine may be lost by volatilization during the extensive rolling resulting in variations of the composition of the ultimate grains. Such large grain propellants have likewise been produced by casting methods, but such prior casting methods have likewise had attending disadvantages. For instance, Silk and Dintelmann in US. Patent 2,417,090 disclose a casting process in which pellets of double base powder having their surface rendered tacky by means of a plasticizer are compressed and heated to form a homogeneous powder grain. Such a process, although well suited for certain types of large grains, is not well adapted for the manufacture of single base grains, requires the use of pressure with the attending hazards, and does not lend itself to the manufacture of grains of irregular configuration such as may be necessary to fit in certain types of rocket motors to provide the desired type of ballistic functioning.
The present invention has as an object the provision of a simplified and improved process for manufacturing rocket powder grains whereby the aforementioned and other disadvantages of prior procedures are overcome. Another object of this invention is to provide a process for producing rocket powder grains of either single or double base composition in which the use of extrusion, rolling, and other pressure methods and devices are eliminated. .A further object is to provide an improved casting process for making rocket powder grains of any desired configuration or design.
, The foregoing objects and advantages, as well as others which will become apparent from the following detailed description, are accomplished in accordance with this invention, generally started, by providing particles or pellets of a propellant, uniformly mixing therewith a plastisol solvent in a s-ufiicient amount to provide a pourable and flowable paste, forming the paste into the shape of a rocket powder grain as by pouring into a mold or by otherwise shaping, and-then maintaining the mixture in the desired shape for a sufficient time to cause the paste to set-up or solidify and thereby form the desired rocket powder grain. The setting-up step is preferably carried out at elevated temperature to hasten the action. By plastisol solvent as used herein is meant a relatively non-volatile liquid which is a slow acting solvent or one having only little or no solvent power for the spherical particles of propellant at low or ordinary room temperatures, but being rapidly acting and having a relatively great solvent power therefor at elevated temperatures.
It has been found that the particles of propellant are advantageously formed by agitating nitrocellulose and a solvent therefor, such as ethyl acetate, with an excess of anon-solvent, such as water, in the presence of a protective colloid, removing the solvent, and thereafter drying the resulting spherical pellets of nitrocellulose. Such a process is described in US. Patent 2,027,114 and for spherical pellets of high density in US. Patent 2,160,626. Such spheres are particularly advantageous in the present invention because of their inherent characteristic of being relatively free-flowing, even in the dry state, and because of their case-hardened surface characteristic which tends to resist initial attack by the solvent. This surface characteristic is undoubtedly the result of a skin effect occasioned by surface tension and removal of the solvent in the formation of the spheres. Other ingredi ents, such as dioctyl phthalate, lead stearate, red lead, centralite, carbon black, dinitrotoluene, and the like, may be incorporated with the nitrocellulose in the formation of the spherical pellets to obtain particular ballistic properties as desired. Using such spherical particles, a relatively free-flowing paste is obtained in'accordance With this invention When'the spheres are mixed with the proper proportion of the plastisol solvent, whereas if irregular shaped particles, such as may be obtained by merely grinding cannon powder or the like, are utilized, the desirable free-flowing characteristics of the paste are not obtained. Although the spheres of propellant may be of any desired size, large diameter spheres require relatively longer periods of time in order to effect their solution and resultant solidification of the grain, whereas with smaller spheres, the time is correspondingly reduced.
It is preferred therefore to utilize spheres having a diameter not greater than about 0.005 inch and preferably of much'smaller diameter, such as 0.001 inch or less.
The ordinary liquid deterrents are generally solvents for nitrocellulose and are admirably suited as the plastisol solvent in the present process, it only being necessary that such deterrent have relatively poor solvent power for the propellant at ordinary room or low temperatures. In other words, the solvent power of such solvent should be insufficient to effect any substantial solution of the propellant at ordinary temperatures during the time required for uniformly mixing the solvent and propellant together and shaping the resultant mixture. Furthermore, if it is desired to prepare double base rocket powder grains, energizing modifiers, such as nitroglycerine, butane triol trinitrate, diglycol dinitrate, ethylene glycol dinitrate, and the like, may be mixed with one or more miscible deterrents, such as dibutyl phthalate, dimethyl sebacate, dibutyl succinate, dibutyl adipate, triacetin, ethyl diphenyl phosphate, tributyl phosphate, and the like, to provide plastisol solvents admirably suited for the purpose. If it is desired toproduce single base rocket powder grains, the energizing modifier may be omitted from the composition and the plastisol solvent will be composed only of a liquid deterrent, such as one of those set forth above or mixtures of them. 1
Other deterrents suitable therefor at temperatures above their 'melting points are dirnethyl phthalate, dioctyl sebacate, ortho nitro biphenyl, butyl benzyl phthalate, i octyl diphenyl phosphate, triethylene glycol di2-.ethyl butyrate (i.e. 'triglycol-dihexoate), and the like.
The amount of plastisol solvent should be such that of the volume of a it forms at least about 25% Substanmixture of the solvent and the propellant.
tially lesser amounts of the plastisol solvent tend toresult in voids or air pockets in the resulting rocket grain and the mixture with such lesser amounts is generally not sufliciently fluid for the purpose. Greater amounts of plastisol solvent may be utilized to good advantage to increase the fluidity of the mixture, vary the ballistic properties of the resulting rocket grain as desired, and insure absence of voids or air spaces in the grains, but
. the amount-utilized should preferably not be sufficicntly great to result in segregation'or settling out of the pro pellant during the period required to cause the mixture to set up. I
In operation, the plastlsol solvent is. preferably desiccated or otherwise treated to reduce any traces of moisture to a minimum, and'both the-propellant-and plastisol solment of air and give the desired design of rocket powder grain.
Such precautions as desiccating and evacuating are preferably observed in order to minimize the possi-. bility of undesirable voids in the resulting rocket powder grain. After the mixture has been given the desired shape, heat is applied to elevate the temperature of the. mixture to a temperature preferably in the range of; about 1 58 C. to 90 C. and such temperature is maintained for a timesuiiicient to cause solution of the propellant and setting-up of the mixture, at which time 'the'temperature may be reduced. As a general rule, the higher the temperature used during this treatment the shorter the period required in order to cause the grain to satisfactorily set up or harden, but precaution should be observed not to exceed the combustion or explosive temperature of the mixture. Grains so formed are of uni form composition throughout, may be of any desired design or configuration, and all pressure extrusion steps and undesirable casting techniques are avoided.
In order that the invention may be further clarified, following is an example illustrating a typical embodiment of the invention. Two hundred fifty parts of nitrocellulose having a nitrogen content of about 12.6% are agitated with 4100 parts of water at about 50 C. to form an aqueous slurry. A suspension of carbon black in ethyl acetate is separately prepared by first thoroughly mixing 0.705 part of carbon black with 100 parts of ethyl acetate. This mixture of carbon black and ethyl acetate is then added to 1250 parts more of ethyl acetate, and the resultant dilute carbon black-ethyl acetate mixture is agitated to insure uniform distribution of the suspended particles of carbon black. Thirty-one and four-tenths parts of dinitrotoluene and 2.8 parts of ethyl centralitc are then added to the carbon black-ethyl acetate mixture. When the dinitrotoluene and the ethyl centralite are dissolved, the resulting mixture is then added to the nitrocellulose slurry while the slurry is under agitation. The temperature is raised to 68 C. and the complete charge vigorously agitated for one hour at which time the nitrocellulose is dissolved. Twenty-five parts of a protective colloid of the type derived from animal protein dispersed in 150 parts of water is then added and the agitation is continued until the nitrocellulose solution is formed into globules of the desired small size. Vigorous. agitation is required in order to form very small particles. The addition of: anemulsi-fying agent, such as the water soluble salts of fatty acids, sulphonated oils, the so-called water-soluble oils, and the like, greatly facilitates the formation of small particles of the nitrocellulose solution, and for this reason, twentyfour parts of a 40% aqueous solution of the sodium sulphate derivative of Z-ethylhexanol is added to the bath. One hundred twenty-five parts of sodium sulfate dissolved in 300 parts of water is added over a one hour period and agitation continued for anadditional three hours. The globules are then hardened to form powder ,grains'by removal of the ethyl acetate during continuous agitation and heating up toabout 99 C. in accordance with the practice set forth in US. Patent 2,027,114 re ferred to, hereinbefore. The resultant spherical pellets of propellant are then air dried at 50 C. and are composed of about 87.7% nitrocellulose, 11.0% 'dinitrotoluene, 0.3% carbon black, and 1.0% ethyl centralite and have an average diameter-of-about 0.001 inch, more or less, depending on the degree of agitation used in the formation thereof.
'About'56.18 parts .byweight of: spherical pellets of propellant such as prepared by the foregoing treating steps are then placed in a sigma blade mixer and the system is evacuated to an absolutepressure of about. ten
millimeters of mercury and so held for about sixteen hours. Meanwhile, about 37 parts by weight of a substantially anhydrous plastisol solvent, composed of 74% by Weight nitroglycerine, 25% by weight dimethyl phthal-' ate and 1% by weight ethyl centralite, is placed in a vessel and the vessel evacuated to an absolute pressure of about 10 millimeters of mercury and'so maintained i for about sixteen hours. The solvent is then added to After the solvent and, propellant are uniformly mixed,
the mixture is then shaped by carefully pouring to avoid entrapmentof air into a mold formed of nitroglycerineresistant plastic such as cellulose acetate, methyl methacrylate, or ethyl cellulose. Inasmuch as the plastisol solvent has a specific gravity of about 1.5, the percent by volume of plastisol solvent in the mixture is about 41.3%. The mold containing the mixture of solvent and propellant is then placed is an oven, heated to about 75 C. and maintained at this temperature until the propellant is substantially dissolved by the solvent and the grain has set up. This solution and setting up of the grain is readily accomplished in a relatively short time, but for instance, may be conveniently let set over night. The exact time of such heat treatment depends, of course, upon the activity of the solvent, the particle size of the propellant, and the effective resistance of the surface of the propellent grains, hereinbefore described as case hardening. For instance, utilizing the propellant and plastisol solvent described above, the mixture, if let stand at the relatively low temperature of about 22 C. will ordinarily set up in about 21 hours. When the grain has set up it is permitted to cool to room temperature and is removed from the mold. I
Rocket powder grains prepared in accordance with the foregoing example are substantially free of undesirable voids, are substantially uniform in composition throughout the grain, and have the strength and other physical properties requisite for rocket powder grains. It will be apparent that the method is relatively simple lending itself to mass production and that no costly apparatus such as is needed for developing high pressures is needed. It will likewise be apparent that the propellant and plastisol solvent may vary appreciably in composition and that rocket powder grains having substantially any desired ballistic characteristics can be prepared in accordance with this invention. While the foregoing embodiment has been set forth in considerable detail, it is to be distinctly understood that many modifications and variations will naturally present themselves to those skilled in the art without departing from the spirit of this invention or the scope of the appended claims.
Having thus described the invention, what I claim and desire to secure by Letters Patent is:
1. In the art of making powder grains by a molding process, the method which comprises preparing a substantially uniform pourable paste by mixing together particles of gelatinized nitrocellulose propellant and a liquid plasticizer for the nitrocellulose in the amount of at least about 25% by volume of the resulting mixture and at a temperature at which substantially no dissolution of the nitrocellulose particles in the plasticizers takes place and thereafter maintaining said composition at atmospheric pressure, and at a temperature at which the nitrocellulose will dissolve, until the nitrocellulose is completely dissolved and the resulting substantially homogeneous mass has solidified into a powder grain.
2. In the art of making powder grains by a molding process, the method for making substantially homogeneous and substantially non-porous propellent grains which comprises preparing a pourable paste having a'substantially uniform composition by mixing together pellets of gelatinized nitrocellulose propellant and a liquid plasticizer for nitrocellulose in the amount of at least about 25 percent by volume of the resulting mixture and at a tem. perature at which substantially no dissolution of the pellets in the plasticizer takes place during said mixing, shaping said paste in a suitable mold, and thereafter maintaining said paste in said mold at atmospheric pressure, and at a temperature at which the nitrocellulose will dissolve, until the nitrocellulose has completely dissolved in said plasticizer and the substantially homogeneous mass has solidified into a propellent powder grain having dimensions and shape conforming substantially to those of said mold.
3.In the art of making powder grains by a molding process, the improved method for making propellent powder grains having a substantially homogeneous nonporous composition which comprises preparing a pourable paste of substantially uniform composition by agitating together pellets of gelatinized nitrocellulose propellant and a liquid plasticizer for nitrocellulose in the amount of at least about 25 percent by volume of the resulting mixture and at a temperature at which substantially no dissolution of the pellets in the plasticizer takes place during said agitation, said plasticizer including in its composition an energizing modifier of the resulting propellent grain, shaping said paste in a suitable mold, and, thereafter, maintaining said paste in said mold at atmospheric pressure and at a temperature at which the nitrocellulose will dissolve until the nitrocellulose has completely dissolved in said plasticizer and the substantially homogeneous mass has solidified into a propellent powder grain having dimensions'and shape conforming substantially to those of said mold.
-4. In the art of making powder grains by a molding process, the improved method for making propellent powder grains having a substantially homogeneous nonporous composition which comprises preparing a pourable paste of substantially uniform composition by agitating together pellets of gelatinized nitrocellulose propellant and a liquid plasticizer for nitrocellulose in the amount of at least about 25 by volume of the resulting mixture and at a temperature at which substantially no dissolution of the pellets in the plasticizer takes place during said agitation, shaping said paste in a suitable mold, and, thereafter, heating said paste in said mold at atmospheric pressure and to a temperature at which the nitrocellulose will dissolve until the nitrocellulose has completely dissolved in said plasticizer and the substantially homogeneous mass has solidified into a propellent powder grain having dimensions and shape conforming substantially to those of said mold.
References Cited in the file of this patent UNITED STATES PATENTS 2,027,114 Olsen et al. -4. Jan. 7, 1936 2,160,626 Schaefer May 30, 1939 2,417,090 Silk et al. Mar. 11, 1947 OTHER REFERENCES I The Condensed Chemical Dictionary, Reinhold Publ, C0rp., N.Y., 4th edition (1950), pp. 490, 527.

Claims (1)

1. IN THE ART OF MAKING POWDER GRANIS BY A MOLDING PROCESS, THE METHOD WHICH COMPRISES PREPARING A SUBSTANTIALLY UNIFORM POURABLE PASTE BY MIXING TOGETHER PARTICLES OF GELATINIZED NITROCELLULOSE PROPELLENT AND A LIQUID PLASTICIZER FOR THE NITROCELLULOSE IN THE AMOUNT OF AT LEAST ABOUT 25% BY VOLUME OF THE RESULTING MIXTURE AND AT A TEMPERATURE AT WHICH SUBSTANTIALLY NO DISSOLUTION OF THE NITROCELLULOSE PARTICLES IN THE PLASTICIZERS TAKES PLACE AND THEREAFTER MAINTAINING SAID COMPOSITION AT ATMOSPHERIC PRESSURE, AND AT A TEMPERATURE AT WHICH THE NITROCELLULOSE WILL DISSOLVE, UNTIL THE NITROCELLULOSE IS COMPLETELY DISSOLVED AND THE RESULTING SUBSTANTIALLY HOMOGENEOUS MASS HAS SOLIDIFIED INTO A POWDER GRAIN.
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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3037417A (en) * 1959-02-12 1962-06-05 Olin Mathieson Explosives
US3108916A (en) * 1959-09-02 1963-10-29 Olin Mathieson Dustless propellent powder containing coated spherical nitrocellulose
US3378611A (en) * 1961-06-09 1968-04-16 Navy Usa Process for production of nitrocellulose propellants
US3808061A (en) * 1964-05-22 1974-04-30 Us Army Nitrocellulose solid propellant composition with load additive to reduce radar attenuation
US3894894A (en) * 1962-06-08 1975-07-15 Us Navy Modified double base propellants with diisocyanate crosslinker

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2027114A (en) * 1932-03-12 1936-01-07 Western Cartridge Co Manufacture of smokeless powders
US2160626A (en) * 1936-01-02 1939-05-30 Western Cartridge Co Explosive
US2417090A (en) * 1944-01-26 1947-03-11 Olin Ind Inc Manufacture of propellent explosives

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2027114A (en) * 1932-03-12 1936-01-07 Western Cartridge Co Manufacture of smokeless powders
US2160626A (en) * 1936-01-02 1939-05-30 Western Cartridge Co Explosive
US2417090A (en) * 1944-01-26 1947-03-11 Olin Ind Inc Manufacture of propellent explosives

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3037417A (en) * 1959-02-12 1962-06-05 Olin Mathieson Explosives
US3108916A (en) * 1959-09-02 1963-10-29 Olin Mathieson Dustless propellent powder containing coated spherical nitrocellulose
US3378611A (en) * 1961-06-09 1968-04-16 Navy Usa Process for production of nitrocellulose propellants
US3894894A (en) * 1962-06-08 1975-07-15 Us Navy Modified double base propellants with diisocyanate crosslinker
US3808061A (en) * 1964-05-22 1974-04-30 Us Army Nitrocellulose solid propellant composition with load additive to reduce radar attenuation

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