US20010042578A1 - Perforated propellant and method of manufacturing same - Google Patents

Perforated propellant and method of manufacturing same Download PDF

Info

Publication number
US20010042578A1
US20010042578A1 US09/882,402 US88240201A US2001042578A1 US 20010042578 A1 US20010042578 A1 US 20010042578A1 US 88240201 A US88240201 A US 88240201A US 2001042578 A1 US2001042578 A1 US 2001042578A1
Authority
US
United States
Prior art keywords
propellant
lacquer
optionally
combinations
group
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.)
Granted
Application number
US09/882,402
Other versions
US6444062B2 (en
Inventor
William O'Meara
Jonathon Howard
Antonio Gonzalez
John Williamson
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.)
General Dynamics Ordnance and Tactical Systems Inc
Original Assignee
General Dynamics Ordnance and Tactical Systems Inc
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 General Dynamics Ordnance and Tactical Systems Inc filed Critical General Dynamics Ordnance and Tactical Systems Inc
Priority to US09/882,402 priority Critical patent/US6444062B2/en
Publication of US20010042578A1 publication Critical patent/US20010042578A1/en
Assigned to GENERAL DYNAMICS ORDNANCE & TACTICAL SYSTEMS, INC. reassignment GENERAL DYNAMICS ORDNANCE & TACTICAL SYSTEMS, INC. CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: PRIMEX TECHNOLOGIES, INC.
Application granted granted Critical
Publication of US6444062B2 publication Critical patent/US6444062B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B25/00Compositions containing a nitrated organic compound
    • C06B25/18Compositions containing a nitrated organic compound the compound being nitrocellulose present as 10% or more by weight of the total composition
    • 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
    • C06B21/0033Shaping the mixture
    • C06B21/0075Shaping the mixture by extrusion

Definitions

  • This invention relates to a propellant composition made from a lacquer and processed to form hollow propellant grains that are useful for ammunition rounds. More particularly, the invention is directed to a low viscosity lacquer that is continuously processed by extrusion to form hollow hardened propellant grains in a liquid slurry.
  • Perforated propellant grains are generally produced by extruding lacquers having between 0 and 20% by weight of solvent. This method of production requires a pressure in the range of between about 1000 and 5000 psi to extrude the lacquer through an extrusion die assembly, and requires large quantities of energy and expensive equipment.
  • the following U.S. Patents are representative of the state of the art.
  • U.S. Pat. No. 4,841,863 entitled, “Saboted, light armour penetrator round with improved powder mix” that issued on Jun. 27, 1989 discloses propellant in the form of spheroidal (substantially spherical) powders and recites that a batch process for the manufacture of spherical powders is disclosed in U.S. Pat. No. 2,027,114 and a continuous process in U.S. Pat. No. 3,679,782.
  • the present invention is directed to a propellant composition made from a lacquer, the lacquer comprising: (a) from about 15 to about 70 wt % of an organic solvent; (b) from about 0.1 to about 2.5 wt % of a stabilizer; (c) optionally, from about 0% to about 40 wt % of an energetic plasticizer; (d) optionally, from about 0 to about 10 wt % of a nonenergetic plasticizer; (e) optionally, from about 0 to about 10 wt % water; (f) optionally, from about 0 to about 15 wt % of additional additives; and balance being nitrocellulose; all weight percents based on the total weight of the composition, and wherein the lacquer has a viscosity of less than 10 million centipoise when processed.
  • the present invention is directed to a propellant composition made from a lacquer, the lacquer consisting essentially of: (a) from about 30 to about 65 wt % of an organic solvent selected from the group consisting of ethyl acetate, ether, acetone, and combinations thereof; (b) from about 0.25 to about 1.5 wt % of a stabilizer selected from the group consisting of diphenylamine, ethyl centralite, diethyldiphenylurea, 2-nitrodiphenylamine, N-nitrosodiphenylamine, and combinations thereof; (c) optionally, from about 5% to about 25 wt % of nitroglycerin as an energetic plasticizer; (d) optionally, from about 0 to about 3 wt % of a nonenergetic plasticizer selected from the group consisting of dibutylphthlate, adipate esters, and combinations thereof; (e) optionally, from about from about 0
  • the present invention is directed to a method for manufacturing perforated propellant grains, comprising the steps of: extruding a propellant lacquer through an extrusion die assembly to form one or more propellant lacquer strands, the extrusion die assembly having a plurality of holes, each of the holes having at least one pin tip positioned therein, the propellant lacquer comprising: (a) from about 15 to about 70 wt % of an organic solvent; (b) from about 0.1 to about 2.5 wt % of a stabilizer; (c) optionally, from about 0% to about 40 wt % of an energetic plasticizer; (d) optionally, from about 0 to about 10 wt % of a nonenergetic plasticizer; (e) optionally, from about 0 to about 10 wt % water; (f) optionally, from about 0 to about 15 wt % of additional additives; and balance being nitrocellulose; all weight percents based on the total weight of
  • the present invention is directed to a propellant grain having outwardly extending ridges.
  • the present invention is directed to a propellant grain having an ellipsoidal cross section.
  • FIG. 1A shows a hollow, tubular portion of the propellant grains of the invention having a single internal perforation
  • FIG. 1B shows the hollow, tubular portion of FIG. 1A in a flattened state
  • FIG. 2A shows an alternative embodiment of the propellant grains of the invention having a plurality of internal perforations
  • FIG. 2B shows the alternative embodiment of FIG. 2A in a flattened state
  • FIG. 3 shows another alternative embodiment of the propellant grains of the invention having outwardly extending ridges.
  • perforated propellant grains may be manufactured continuously from a specific lacquer composition in a safe, cost-effective, and efficient manner.
  • the continuous preparation of a perforated propellant produces a strand having a generally cylindrical shape with one or more inner concentric hollow cylinders (termed perforations) arranged parallel to the longitudinal axis of the strand.
  • the produced strands may be cut to desired sizes, may be flattened to form ellipsoid shapes, or may be formed to specific configurations (e.g., with outwardly extending ridges).
  • the cut strands (grains) are made from a composition that requires less pressure to extrude during the manufacturing process, thereby considerably reducing energy and equipment costs.
  • perforation refers to a tubular space (hollow cylinder) oriented parallel to the longitudinal axis of the strand or grain.
  • the propellant of the present invention is made from a lacquer comprising (a) an organic solvent; (b) a stabilizer; (c) optionally, an energetic plasticizer; (d) optionally, a nonenergetic plasticizer; (e) optionally, water; and (f) optionally, additional additives; and the balance being nitrocellulose.
  • a lacquer comprising (a) an organic solvent; (b) a stabilizer; (c) optionally, an energetic plasticizer; (d) optionally, a nonenergetic plasticizer; (e) optionally, water; and (f) optionally, additional additives; and the balance being nitrocellulose.
  • Solvents that are useful in the composition and method of the present invention include ethyl acetate, ether, acetone, and combinations thereof.
  • a preferred solvent is ethyl acetate.
  • the amount of solvent used in the composition of the invention ranges from about 15 to about 70 wt %, and more preferably from about 30 to about 65 wt %, based on the total weight of the composition.
  • the lacquer composition of the invention also includes one or more stabilizers.
  • suitable stabilizers include diphenylamine, ethyl centralite, diethyldiphenylurea, 2-nitrodiphenylamine, N-nitrosodiphenylamine, and combinations thereof.
  • Useful amounts of the stabilizers in the composition of the present invention generally range from 0.1 wt % to about 2.5 wt %, and more preferably from about 0.25 wt % to about 1.5 wt %, based on the total weight of the composition.
  • the balance of the lacquer composition of the invention is nitrocellulose.
  • the nitrocellulose used in the present invention may be in any form. However, in a preferred embodiment, the nitrocellulose is completely dissolved in one or more solvents.
  • the lacquer composition of the invention includes an energetic plasticizer such as nitroglycerin, ethylene glycol esters, methylene glycols, glycol esters, formyl acetal (bis(2,2-dinitropropyl)formal acetal) and combinations thereof.
  • an energetic plasticizer such as nitroglycerin, ethylene glycol esters, methylene glycols, glycol esters, formyl acetal (bis(2,2-dinitropropyl)formal acetal) and combinations thereof.
  • a useful working range is from about 0% to about 40 wt %, and more preferably from about 5 to about 25 wt %, based on the total weight of the composition.
  • the lacquer composition of the invention also includes a nonenergetic plasticizer such as dibutylphthlate, adipate esters, and combinations thereof.
  • a nonenergetic plasticizer such as dibutylphthlate, adipate esters, and combinations thereof.
  • DBP dibutylphthlate
  • the nonenergetic plasticizer component comprises from about 0 to about 10 wt %, and more preferably from about 0 wt % to about 3 wt %, based on the total weight of the composition.
  • the lacquer composition of the invention may also include optional additives, including lubricants, such as graphite; coolants, such as magnesium carbonate; barrel wear additives, such as tin dioxide, titanium dioxide, calcium bicarbonate, and the like; flash suppressants, such as potassium salts; decoppering agents, such as bismuth and tin dioxides; and energetic solids known in the art, such as RDX, HMX, CL20, nitroguanidine, and the like.
  • lubricants such as graphite
  • coolants such as magnesium carbonate
  • barrel wear additives such as tin dioxide, titanium dioxide, calcium bicarbonate, and the like
  • flash suppressants such as potassium salts
  • decoppering agents such as bismuth and tin dioxides
  • energetic solids known in the art such as RDX, HMX, CL20, nitroguanidine, and the like.
  • additives may be present in amounts effective for desired results.
  • Such additives such as deterrents may influence burn rate, burn temperature, extrusion performance or other properties of manufacture or use.
  • the lacquer composition of the present invention is prepared by mixing the above ingredients in an agitated kettle until a homogeneous lacquer is produced.
  • An aqueous process for the manufacture of perforated propellant begins with the formation of a propellant lacquer as described above.
  • the extrusion viscosity of the lacquer should be less than 10 million centipoise, and is preferably between 1 million and 3 million centipoise.
  • the lacquer of the invention may be pumped through a perforated extrusion die assembly as described below at a pressure of between 30 and 200 pounds per square inch. This method is to be contrasted with conventionally extruded lacquers having between 0 and 15% by weight of solvent that require a pressure in the range of between about 1000 and 5000 psi to extrude.
  • One suitable lacquer has the composition, by weight, of: Component Weight % Organic solvent 15%-70% Energetic Plasticizer 0-40% Stabilizer 0.1%-2.5% Nonenergetic Plasticizer 0-10% Water 0-10% Nitrocellulose balance
  • the lacquer has the composition, by weight, of: Component Weight % Ethyl Acetate 30%-65% Nitroglycerin 5%-25% Stabilizer 0.25%-1.5% Dibutylphthlate 0-3% Water 1%-4% Nitrocellulose balance
  • lacquers formed from these components function as a Newtonian shear thinning fluid.
  • the lacquer made according to the method of the invention has a low viscosity and is easily pumped through the extrusion die assembly and thereby requiring less energy and equipment costs.
  • the lacquer is pumped through an extrusion die assembly and into an aqueous solution, referred to as liquor.
  • the extrusion die assembly has a plurality of die holes, each of which has at least one pin tip positioned therein to produce grains having hollow cores (perforations).
  • the liquor is preferably water-based, and generally maintained at a temperature of between about 35 and 80° C. Up to about 6% by weight of a salt (a dewatering agent) and up to about 6% by weight of a surfactant (an antiagglomerating agent) may be added to the liquor.
  • a suitable salt is sodium sulfate, and a suitable surfactant is a colloid.
  • Rotating knives adjacent to the base surface of the plate cut the lacquer strand into perforated cylinders of lengths which are controlled by the rate of revolution of the rotating knives and/or by controlling the pump speed.
  • the cut perforated propellant grains have a length-to-diameter ratio of approximately 2:1.
  • the liquor is then used to safely transport the perforated propellant through both the dewatering and solvent removal and grain hardening stages.
  • dewatering To control dewatering, temperature, time, residual solvent and salt concentration in the liquor are controlled. Typically dewatering involves heating the liquor to a temperature of between about 35° C. and 80° C., and preferably of between 40° C. and 60° C.
  • the perforated grains After dewatering, and/or while dewatering, the perforated grains then go through a solvent removal process.
  • This process can begin with the addition of solventless liquor to the system. This step dilutes the solvent in the liquor and results in solvent removal (leaching) from the perforated grains at a controllable rate.
  • This method of solvent removal can be used to remove enough solvent such that the perforated grains become tough and leathery, however in some cases it may be desirable to leave up to about 40% solvent by weight in the grained material.
  • the perforated grains can be heated without softening to the point of deformation.
  • the temperature of the perforated grains and liquor is increased and/or vacuum is applied until the solvent is removed to a level sufficient enough for storage.
  • Heating may be up to any temperature up to or less than the boiling point of water, and is generally dependent on whether a vacuum is employed. At atmospheric pressure, a temperature of up to about 99° C. may be utilized. At 11.5 inches of pressure, the maximum temperature is about 86° C.
  • the perforated grains can be further impregnated or coated, such as with nitroglycerin (an energetic plasticizer) or with a deterrent, and dried for use to form the finished propellant.
  • nitroglycerin an energetic plasticizer
  • deterrent a deterrent
  • FIGS. 1A, 1B, 2 A, 2 B, and 3 Exemplary shapes for propellant grains are illustrated in FIGS. 1A, 1B, 2 A, 2 B, and 3 .
  • FIG. 1A shows a grain having a circular cross section and a perforation 40 centered in the strand cross section and running parallel to the longitudinal axis of the strand.
  • the grain shown in FIG. 1A can be compressed to form a grain having an ellipsoidal cross section as shown in FIG. 1B.
  • the flattened propellant grain with ellipsoidal cross section of FIG. 1B provides for increased packing density for increased propellant weight capability when compared to the grain with a circular cross section of FIG. 1A.
  • the FIG. 1B shape also has utility to decrease temperature sensitivity (the tendency of a propellant to burn quicker at higher temperatures and slower at lower temperatures).
  • FIGS. 2A and 2B show the addition of multiple perforations to influence burn characteristics of the grains.
  • the extrusion die assembly would have a plurality of pin tips to form the desired number of perforations through the strand.
  • the configuration of FIG. 2B having an ellipsoidal cross section is made in a similar manner to the grain shown in FIG. 1B.
  • FIG. 3 illustrates a ridged, perforated, propellant grain with a geometry that provides for a low packing density for a lower propellant charge weight and also fills a cartridge volume, reducing ullage.
  • the ridged propellant grains are characterized by superior ignition and flame permeability when compared to similarly configured perforated propellants without the ridges. The reduction in ullage provides enhanced safety and ballistic uniformity.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Paints Or Removers (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Telephone Function (AREA)
  • Extrusion Moulding Of Plastics Or The Like (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)

Abstract

The present invention is directed to a propellant composition made from a lacquer, the lacquer comprising: (a) from about 15 to about 70 wt % of an organic solvent; (b) from about 0.1 to about 2.5 wt % of a stabilizer; (c) optionally, from about 0% to about 40 wt % of an energetic plasticizer; (d) optionally, from about 0 to about 10 wt % of a nonenergetic plasticizer; (e) optionally, from about 0 to about 10 wt % water; (f) optionally, from about 0 to about 15 wt % of additional additives; and balance being nitrocellulose; all weight percents based on the total weight of the composition, and wherein the lacquer has a viscosity of less than 10 million centipoise when processed. The present invention is also directed to an efficient and safe method of making perforated propellant grains using the above lacquer composition, as well as propellant grains having ellipsoidal cross sections or outwardly extending ridges.

Description

  • This application claims the benefit of Provisional Application Ser. No. 60/121,208 filed on Feb. 23, 1999.[0001]
  • BACKGROUND OF THE INVENTION
  • 1. Field of the Invention [0002]
  • This invention relates to a propellant composition made from a lacquer and processed to form hollow propellant grains that are useful for ammunition rounds. More particularly, the invention is directed to a low viscosity lacquer that is continuously processed by extrusion to form hollow hardened propellant grains in a liquid slurry. [0003]
  • 2. Description of Related Art [0004]
  • Perforated propellant grains are generally produced by extruding lacquers having between 0 and 20% by weight of solvent. This method of production requires a pressure in the range of between about 1000 and 5000 psi to extrude the lacquer through an extrusion die assembly, and requires large quantities of energy and expensive equipment. The following U.S. Patents are representative of the state of the art. [0005]
  • U.S. Pat. No. 5,821,449 entitled, “Propellant grain geometry for controlling ullage and increasing flame permeability” that issued on Oct. 13, 1998 discloses hollow grain propellants for use in lightweight training rounds. [0006]
  • U.S. Pat. No. 4,841,863 entitled, “Saboted, light armour penetrator round with improved powder mix” that issued on Jun. 27, 1989 discloses propellant in the form of spheroidal (substantially spherical) powders and recites that a batch process for the manufacture of spherical powders is disclosed in U.S. Pat. No. 2,027,114 and a continuous process in U.S. Pat. No. 3,679,782. [0007]
  • U.S. Pat. No. 5,524,544 entitled, “Nitrocellulose propellant containing a cellulosic burn rate modifier” that issued on Jun. 11, 1996 and U.S. Pat. No. 5,510,062 entitled, “Method of producing a nitrocellulose propellant containing a cellulosic burn rate modifier infiltrated therein that issued on Apr. 23, 1996 disclose a solvent process for the manufacture of propellant grains where a burn rate deterrent is gradationally dispersed within the propellant with the greatest concentration of deterrent at the particulate periphery. [0008]
  • U.S. Pat. Nos. 2,027,114; 3,679,782; 4,841,863; 5,510,062; 5,524,544 and 5,821,449 are all incorporated by reference in their entireties herein. [0009]
  • Accordingly, what is needed in the art is a lacquer composition and method of manufacturing that efficiently produces perforated propellant grains in a safe and economical manner, and at a lower extrusion pressure than presently used. The present invention is believed to be an answer to that need. [0010]
  • SUMMARY OF THE INVENTION
  • In one aspect, the present invention is directed to a propellant composition made from a lacquer, the lacquer comprising: (a) from about 15 to about 70 wt % of an organic solvent; (b) from about 0.1 to about 2.5 wt % of a stabilizer; (c) optionally, from about 0% to about 40 wt % of an energetic plasticizer; (d) optionally, from about 0 to about 10 wt % of a nonenergetic plasticizer; (e) optionally, from about 0 to about 10 wt % water; (f) optionally, from about 0 to about 15 wt % of additional additives; and balance being nitrocellulose; all weight percents based on the total weight of the composition, and wherein the lacquer has a viscosity of less than 10 million centipoise when processed. [0011]
  • In another aspect, the present invention is directed to a propellant composition made from a lacquer, the lacquer consisting essentially of: (a) from about 30 to about 65 wt % of an organic solvent selected from the group consisting of ethyl acetate, ether, acetone, and combinations thereof; (b) from about 0.25 to about 1.5 wt % of a stabilizer selected from the group consisting of diphenylamine, ethyl centralite, diethyldiphenylurea, 2-nitrodiphenylamine, N-nitrosodiphenylamine, and combinations thereof; (c) optionally, from about 5% to about 25 wt % of nitroglycerin as an energetic plasticizer; (d) optionally, from about 0 to about 3 wt % of a nonenergetic plasticizer selected from the group consisting of dibutylphthlate, adipate esters, and combinations thereof; (e) optionally, from about from about 0 to about 4 wt % water; (f) optionally, from about 0 to about 15 wt % of additional additives selected from the group consisting of lubricants; coolants; barrel wear additives; flash suppressants; decoppering agents; energetic solids, and combinations thereof; and balance being nitrocellulose; wherein all weight percents are based on the total weight of the composition, and wherein the lacquer has a viscosity of between 1 million and 3 million centipoise. [0012]
  • In another aspect, the present invention is directed to a method for manufacturing perforated propellant grains, comprising the steps of: extruding a propellant lacquer through an extrusion die assembly to form one or more propellant lacquer strands, the extrusion die assembly having a plurality of holes, each of the holes having at least one pin tip positioned therein, the propellant lacquer comprising: (a) from about 15 to about 70 wt % of an organic solvent; (b) from about 0.1 to about 2.5 wt % of a stabilizer; (c) optionally, from about 0% to about 40 wt % of an energetic plasticizer; (d) optionally, from about 0 to about 10 wt % of a nonenergetic plasticizer; (e) optionally, from about 0 to about 10 wt % water; (f) optionally, from about 0 to about 15 wt % of additional additives; and balance being nitrocellulose; all weight percents based on the total weight of the composition, and wherein the lacquer has an extrusion viscosity of less than 10 million centipoise; cutting the propellant lacquer strand to a desired dimension to form perforated propellant grains; suspending the perforated propellant grains in a water based liquor; removing the organic solvent and water from the perforated propellant grains; and hardening the perforated propellant grains. [0013]
  • In another aspect, the present invention is directed to a propellant grain having outwardly extending ridges. [0014]
  • In another aspect, the present invention is directed to a propellant grain having an ellipsoidal cross section. [0015]
  • These and other aspects will be more fully understood from the following detailed description of the invention. [0016]
  • DESCRIPTION OF THE DRAWINGS
  • The invention will be more fully understood from the following detailed description taken in conjunction with the accompanying drawings in which: [0017]
  • FIG. 1A shows a hollow, tubular portion of the propellant grains of the invention having a single internal perforation; [0018]
  • FIG. 1B shows the hollow, tubular portion of FIG. 1A in a flattened state; [0019]
  • FIG. 2A shows an alternative embodiment of the propellant grains of the invention having a plurality of internal perforations; [0020]
  • FIG. 2B shows the alternative embodiment of FIG. 2A in a flattened state; and [0021]
  • FIG. 3 shows another alternative embodiment of the propellant grains of the invention having outwardly extending ridges.[0022]
  • DETAILED DESCRIPTION OF THE INVENTION
  • It has now been found that perforated propellant grains may be manufactured continuously from a specific lacquer composition in a safe, cost-effective, and efficient manner. The continuous preparation of a perforated propellant produces a strand having a generally cylindrical shape with one or more inner concentric hollow cylinders (termed perforations) arranged parallel to the longitudinal axis of the strand. The produced strands may be cut to desired sizes, may be flattened to form ellipsoid shapes, or may be formed to specific configurations (e.g., with outwardly extending ridges). The cut strands (grains) are made from a composition that requires less pressure to extrude during the manufacturing process, thereby considerably reducing energy and equipment costs. [0023]
  • As defined herein, the term “perforation” refers to a tubular space (hollow cylinder) oriented parallel to the longitudinal axis of the strand or grain. [0024]
  • As indicated above, the propellant of the present invention is made from a lacquer comprising (a) an organic solvent; (b) a stabilizer; (c) optionally, an energetic plasticizer; (d) optionally, a nonenergetic plasticizer; (e) optionally, water; and (f) optionally, additional additives; and the balance being nitrocellulose. Each of these components is discussed in detail below. [0025]
  • Solvents that are useful in the composition and method of the present invention include ethyl acetate, ether, acetone, and combinations thereof. A preferred solvent is ethyl acetate. Preferably, the amount of solvent used in the composition of the invention ranges from about 15 to about 70 wt %, and more preferably from about 30 to about 65 wt %, based on the total weight of the composition. [0026]
  • The lacquer composition of the invention also includes one or more stabilizers. Examples of suitable stabilizers include diphenylamine, ethyl centralite, diethyldiphenylurea, 2-nitrodiphenylamine, N-nitrosodiphenylamine, and combinations thereof. Useful amounts of the stabilizers in the composition of the present invention generally range from 0.1 wt % to about 2.5 wt %, and more preferably from about 0.25 wt % to about 1.5 wt %, based on the total weight of the composition. [0027]
  • The balance of the lacquer composition of the invention is nitrocellulose. The nitrocellulose used in the present invention may be in any form. However, in a preferred embodiment, the nitrocellulose is completely dissolved in one or more solvents. [0028]
  • Optionally, the lacquer composition of the invention includes an energetic plasticizer such as nitroglycerin, ethylene glycol esters, methylene glycols, glycol esters, formyl acetal (bis(2,2-dinitropropyl)formal acetal) and combinations thereof. If such an energetic plasticizer is included in the composition, a useful working range is from about 0% to about 40 wt %, and more preferably from about 5 to about 25 wt %, based on the total weight of the composition. [0029]
  • Optionally, the lacquer composition of the invention also includes a nonenergetic plasticizer such as dibutylphthlate, adipate esters, and combinations thereof. A preferred nonenergetic plasticizer is DBP (dibutylphthlate). Generally, the nonenergetic plasticizer component comprises from about 0 to about 10 wt %, and more preferably from about 0 wt % to about 3 wt %, based on the total weight of the composition. [0030]
  • The lacquer composition of the invention may also include optional additives, including lubricants, such as graphite; coolants, such as magnesium carbonate; barrel wear additives, such as tin dioxide, titanium dioxide, calcium bicarbonate, and the like; flash suppressants, such as potassium salts; decoppering agents, such as bismuth and tin dioxides; and energetic solids known in the art, such as RDX, HMX, CL20, nitroguanidine, and the like. [0031]
  • Other additives may be present in amounts effective for desired results. Such additives such as deterrents may influence burn rate, burn temperature, extrusion performance or other properties of manufacture or use. [0032]
  • The lacquer composition of the present invention is prepared by mixing the above ingredients in an agitated kettle until a homogeneous lacquer is produced. [0033]
  • An aqueous process for the manufacture of perforated propellant begins with the formation of a propellant lacquer as described above. The extrusion viscosity of the lacquer should be less than 10 million centipoise, and is preferably between 1 million and 3 million centipoise. At this viscosity, the lacquer of the invention may be pumped through a perforated extrusion die assembly as described below at a pressure of between 30 and 200 pounds per square inch. This method is to be contrasted with conventionally extruded lacquers having between 0 and 15% by weight of solvent that require a pressure in the range of between about 1000 and 5000 psi to extrude. [0034]
  • One suitable lacquer has the composition, by weight, of: [0035]
    Component Weight %
    Organic solvent 15%-70%
    Energetic Plasticizer   0-40%
    Stabilizer 0.1%-2.5%
    Nonenergetic Plasticizer   0-10%
    Water   0-10%
    Nitrocellulose balance
  • In a preferred embodiment, the lacquer has the composition, by weight, of: [0036]
    Component Weight %
    Ethyl Acetate  30%-65%
    Nitroglycerin  5%-25%
    Stabilizer 0.25%-1.5%
    Dibutylphthlate   0-3%
    Water  1%-4%
    Nitrocellulose balance
  • Without wishing to be bound by any particular theory, it is believed that the lacquers formed from these components function as a Newtonian shear thinning fluid. The lacquer made according to the method of the invention has a low viscosity and is easily pumped through the extrusion die assembly and thereby requiring less energy and equipment costs. [0037]
  • In order to produce the perforated propellant, the lacquer is pumped through an extrusion die assembly and into an aqueous solution, referred to as liquor. The extrusion die assembly has a plurality of die holes, each of which has at least one pin tip positioned therein to produce grains having hollow cores (perforations). The liquor is preferably water-based, and generally maintained at a temperature of between about 35 and 80° C. Up to about 6% by weight of a salt (a dewatering agent) and up to about 6% by weight of a surfactant (an antiagglomerating agent) may be added to the liquor. A suitable salt is sodium sulfate, and a suitable surfactant is a colloid. Rotating knives adjacent to the base surface of the plate cut the lacquer strand into perforated cylinders of lengths which are controlled by the rate of revolution of the rotating knives and/or by controlling the pump speed. Generally, the cut perforated propellant grains have a length-to-diameter ratio of approximately 2:1. The liquor is then used to safely transport the perforated propellant through both the dewatering and solvent removal and grain hardening stages. [0038]
  • To control dewatering, temperature, time, residual solvent and salt concentration in the liquor are controlled. Typically dewatering involves heating the liquor to a temperature of between about 35° C. and 80° C., and preferably of between 40° C. and 60° C. [0039]
  • After dewatering, and/or while dewatering, the perforated grains then go through a solvent removal process. This process can begin with the addition of solventless liquor to the system. This step dilutes the solvent in the liquor and results in solvent removal (leaching) from the perforated grains at a controllable rate. This method of solvent removal can be used to remove enough solvent such that the perforated grains become tough and leathery, however in some cases it may be desirable to leave up to about 40% solvent by weight in the grained material. At this stage, the perforated grains can be heated without softening to the point of deformation. [0040]
  • To harden the grains, the temperature of the perforated grains and liquor is increased and/or vacuum is applied until the solvent is removed to a level sufficient enough for storage. Heating may be up to any temperature up to or less than the boiling point of water, and is generally dependent on whether a vacuum is employed. At atmospheric pressure, a temperature of up to about 99° C. may be utilized. At 11.5 inches of pressure, the maximum temperature is about 86° C. [0041]
  • The perforated grains can be further impregnated or coated, such as with nitroglycerin (an energetic plasticizer) or with a deterrent, and dried for use to form the finished propellant. [0042]
  • Changing the shape of the die hole of the extrusion die assembly changes the outer surface configuration of the grains and influences burn rate and performance. Exemplary shapes for propellant grains are illustrated in FIGS. 1A, 1B, [0043] 2A, 2B, and 3. FIG. 1A shows a grain having a circular cross section and a perforation 40 centered in the strand cross section and running parallel to the longitudinal axis of the strand. The grain shown in FIG. 1A can be compressed to form a grain having an ellipsoidal cross section as shown in FIG. 1B. The flattened propellant grain with ellipsoidal cross section of FIG. 1B, provides for increased packing density for increased propellant weight capability when compared to the grain with a circular cross section of FIG. 1A. The FIG. 1B shape also has utility to decrease temperature sensitivity (the tendency of a propellant to burn quicker at higher temperatures and slower at lower temperatures).
  • FIGS. 2A and 2B show the addition of multiple perforations to influence burn characteristics of the grains. In this embodiment, the extrusion die assembly would have a plurality of pin tips to form the desired number of perforations through the strand. The configuration of FIG. 2B having an ellipsoidal cross section is made in a similar manner to the grain shown in FIG. 1B. [0044]
  • FIG. 3 illustrates a ridged, perforated, propellant grain with a geometry that provides for a low packing density for a lower propellant charge weight and also fills a cartridge volume, reducing ullage. The ridged propellant grains are characterized by superior ignition and flame permeability when compared to similarly configured perforated propellants without the ridges. The reduction in ullage provides enhanced safety and ballistic uniformity. [0045]
  • While the invention has been described in combination with embodiments thereof, it is evident that many alternatives, modifications and variations will be apparent to those skilled in the art in light of the foregoing description. Accordingly, it is intended to embrace all such alternatives, modifications and variations as fall within the spirit and broad scope of the appended claims. All patent applications, patents, and other publications cited herein are incorporated by reference in their entireties. [0046]

Claims (18)

What is claimed is:
1. A propellant composition made from a lacquer, said lacquer comprising:
(a) from about 15 to about 70 wt % of an organic solvent;
(b) from about 0.1 to about 2.5 wt % of a stabilizer;
(c) optionally, from about 0% to about 40 wt % of an energetic plasticizer;
(d) optionally, from about 0 to about 10 wt % of a nonenergetic plasticizer;
(e) optionally, from about 0 to about 10 wt % water;
(f) optionally, from about 0 to about 15 wt % of additional additives; and
balance being nitrocellulose; all weight percents based on the total weight of said composition, and wherein said lacquer has a viscosity of less than 10 million centipoise when processed.
2. The propellant composition of
claim 1
, wherein said organic solvent is selected from the group consisting of ethyl acetate, ether, acetone, and combinations thereof.
3. The propellant composition of
claim 1
, wherein said stabilizer is selected from the group consisting of diphenylamine, ethyl centralite, diethyldiphenylurea, 2-nitrodiphenylamine, N-nitrosodiphenylamine, and combinations thereof.
4. The propellant composition of
claim 1
, wherein said optional energetic plasticizer is selected from the group consisting of nitroglycerin, ethylene glycol esters, methylene glycols, glycol esters, bis(2,2-dinitropropyl)formal acetal, and combinations thereof.
5. The propellant composition of
claim 1
, wherein said optional nonenergetic plasticizer is selected from the group consisting of dibutylphthlate, adipate esters, and combinations thereof.
6. The propellant composition of
claim 1
, wherein said optional additional additives are selected from the group consisting of lubricants; coolants; barrel wear additives; flash suppressants; decoppering agents; energetic solids, and combinations thereof.
7. A propellant composition made from a lacquer, said lacquer consisting essentially of:
(a) from about 30 to about 65 wt % of an organic solvent selected from the group consisting of ethyl acetate, ether, acetone, and combinations thereof;
(b) from about 0.25 to about 1.5 wt % of a stabilizer selected from the group consisting of diphenylamine, ethyl centralite, diethyldiphenylurea, 2-nitrodiphenylamine, N-nitrosodiphenylamine, and combinations thereof;
(c) optionally, from about 5% to about 25 wt % of nitroglycerin as an energetic plasticizer;
(d) optionally, from about 0 to about 3 wt % of a nonenergetic plasticizer selected from the group consisting of dibutylphthlate, adipate esters, and combinations thereof;
(e) optionally, from about from about 0 to about 4 wt % water;
(f) optionally, from about 0 to about 15 wt % of additional additives selected from the group consisting of lubricants; coolants; barrel wear additives; flash suppressants; decoppering agents; energetic solids, and combinations thereof; and
balance being nitrocellulose;
wherein all weight percents are based on the total weight of said composition, and wherein said lacquer has a viscosity of between 1 million and 3 million centipoise.
8. A method for manufacturing perforated propellant grains, comprising the steps of:
extruding a propellant lacquer through an extrusion die assembly to form one or more propellant lacquer strands, said extrusion die assembly having a plurality of holes, each of said holes having at least one pin tip positioned therein, said propellant lacquer comprising:
(a) from about 15 to about 70 wt % of an organic solvent;
(b) from about 0.1 to about 2.5 wt % of a stabilizer;
(c) optionally, from about 0% to about 40 wt % of an energetic plasticizer;
(d) optionally, from about 0 to about 10 wt % of a nonenergetic plasticizer;
(e) optionally, from about 0 to about 10 wt % water;
(f) optionally, from about 0 to about 15 wt % of additional additives; and
balance being nitrocellulose; all weight percents based on the total weight of said composition, and wherein said lacquer has an extrusion viscosity of less than 10 million centipoise;
cutting said propellant lacquer strand to a desired dimension to form perforated propellant grains;
suspending said perforated propellant grains in a water based liquor;
removing said organic solvent and water from said perforated propellant grains; and
hardening said perforated propellant grains.
9. The method of
claim 8
, wherein said perforated propellant grains have a circular cross-section.
10. The method of
claim 8
, further comprising the step of compressing said perforated propellant grains to form perforated propellant grains having an ellipsoidal cross section.
11. The method of
claim 8
, wherein said plurality of holes and said pin tips of said extrusion die assembly are arranged to form perforated propellant grains having outwardly extending ridges.
12. The method of
claim 8
, wherein said organic solvent is selected from the group consisting of ethyl acetate, ether, acetone, and combinations thereof.
13. The method of
claim 8
, wherein said stabilizer is selected from the group consisting of diphenylamine, ethyl centralite, diethyldiphenylurea, 2-nitrodiphenylamine, N-nitrosodiphenylamine, and combinations thereof.
14. The method of
claim 8
, wherein said optional energetic plasticizer is selected from the group consisting of nitroglycerin, ethylene glycol esters, methylene glycols, glycol esters, bis(2,2-dinitropropyl)formal acetal, and combinations thereof.
15. The method of
claim 8
, wherein said optional nonenergetic plasticizer is selected from the group consisting of dibutylphthlate, adipate esters, and combinations thereof.
16. The method of
claim 8
, wherein said optional additional additives are selected from the group consisting of lubricants; coolants; barrel wear additives; flash suppressants; decoppering agents; energetic solids, and combinations thereof.
17. A perforated propellant grain having outwardly extending ridges.
18. A perforated propellant grain having an ellipsoidal cross section.
US09/882,402 1999-02-23 2001-06-16 Perforated propellant and method of manufacturing same Expired - Lifetime US6444062B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US09/882,402 US6444062B2 (en) 1999-02-23 2001-06-16 Perforated propellant and method of manufacturing same

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US12120899P 1999-02-23 1999-02-23
US50550100A 2000-02-17 2000-02-17
US09/882,402 US6444062B2 (en) 1999-02-23 2001-06-16 Perforated propellant and method of manufacturing same

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US50550100A Division 1999-02-23 2000-02-17

Publications (2)

Publication Number Publication Date
US20010042578A1 true US20010042578A1 (en) 2001-11-22
US6444062B2 US6444062B2 (en) 2002-09-03

Family

ID=26819218

Family Applications (1)

Application Number Title Priority Date Filing Date
US09/882,402 Expired - Lifetime US6444062B2 (en) 1999-02-23 2001-06-16 Perforated propellant and method of manufacturing same

Country Status (7)

Country Link
US (1) US6444062B2 (en)
EP (1) EP1031547B1 (en)
AT (1) ATE298736T1 (en)
DE (1) DE60021001T2 (en)
DK (1) DK1031547T3 (en)
ES (1) ES2244368T3 (en)
PT (1) PT1031547E (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090223611A1 (en) * 2006-02-09 2009-09-10 General Dynamics Ordnance And Tactical Systems- Canada Valleyfield Inc. Black Powder Substitutes for Small Caliber Firearms
US8597444B1 (en) * 2007-05-23 2013-12-03 The United States Of America As Represented By The Secretary Of The Army Foamed celluloid combustible material
US8778104B1 (en) * 2008-04-22 2014-07-15 The United States Of America As Represented By The Secretary Of The Navy Insensitive gun propellant, ammunition round assembly, armament system, and related methods
US20150284301A1 (en) * 2013-08-16 2015-10-08 General Dynamics Ordnance And Tactical Systems - Canada Valleyfield Inc. Method of manufacturing multi-layered propellant grains
RU2627408C1 (en) * 2016-07-04 2017-08-08 Федеральное казенное предприятие "Государственный научно-исследовательский институт химических продуктов" (ФКП "ГосНИИХП") Method of producing coarse pellet powder

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2235813T3 (en) * 2000-06-15 2005-07-16 Nitrochemie Wimmis Ag PROCEDURE FOR THE MANUFACTURE OF A HIGHLY ENERGETIC FUNCTIONAL MATERIAL.
US20090208647A1 (en) * 2000-06-15 2009-08-20 Nitrochemie Wimmis Ag Method for producing a funtional, high-energy material
SE518867C2 (en) * 2001-04-02 2002-12-03 Nexplo Bofors Ab Powder and methods and apparatus for making the same
DE10152396A1 (en) * 2001-10-24 2003-05-15 Bowas Ag Fuer Industrievertrie Manufacture of anhydrous nitrocellulose and eyplosive substances in spheroidal form
AU2003284433A1 (en) * 2002-11-22 2004-06-18 Nippon Kayaku Kabushiki Kaisha Gas generating agent, process for production thereof, and gas generators for air bags
US7896990B1 (en) 2004-02-20 2011-03-01 The United States Of America As Represented By The Secretary Of The Navy Burn rate nanotube modifiers
DK1616845T3 (en) * 2004-07-16 2014-02-03 Nitrochemie Wimmis Ag Pourable pourable powder
SE529752C2 (en) * 2006-04-20 2007-11-13 Eurenco Bofors Ab Powder loads of multi-perforated rod powder for high-speed projectiles and production thereof
EP1886983A1 (en) * 2006-08-09 2008-02-13 Russell R. Nickel Method for manufacture of microcrystalline nitrocellulose
RU2318789C1 (en) * 2006-10-16 2008-03-10 Общество с ограниченной ответственностью "ИФОХИМ" Explosive modifier
US7842144B1 (en) * 2007-06-01 2010-11-30 The United States Of America As Represented By The Secretary Of The Navy Methods of making double base casting powder
WO2011153655A2 (en) * 2011-09-15 2011-12-15 Nitrochemie Wimmis Ag Nitroglycerine-free multi-perforated high-performing propellant system

Family Cites Families (39)

* 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
US2292469A (en) * 1939-09-25 1942-08-11 Western Cartridge Co Smokeless powder
US3201500A (en) * 1951-11-16 1965-08-17 Olin Mathieson Propellant powder making process
US3223756A (en) * 1957-12-20 1965-12-14 Hercules Powder Co Ltd Smokeless powder manufacture
US3163567A (en) * 1963-04-18 1964-12-29 Olin Mathieson Production of disc-shaped nitrocellulose
US3392669A (en) * 1966-01-24 1968-07-16 Army Usa Erosion reducer
US4172866A (en) * 1968-03-29 1979-10-30 Hercules Incorporated Drying process for casting powders
BE759229A (en) * 1969-11-20 1971-05-21 Olin Corp PERFECTED PROCESS FOR FORMING SPHERICAL GRAINS OF PROPULSIVE POWDER
US3989776A (en) * 1970-10-07 1976-11-02 The United States Of America As Represented By The Secretary Of The Army Process for preparing double base propellants containing ballistic modifier
US4001287A (en) * 1970-10-07 1977-01-04 The United States Of America As Represented By The Secretary Of The Army Reaction product of normal lead beta resorcylate and monobasic cupric salicylate
US3855373A (en) * 1972-09-19 1974-12-17 Us Army New process for making nitrocellulose base propellants
DE2461646C2 (en) * 1974-12-27 1984-01-05 Dynamit Nobel Ag, 5210 Troisdorf Process for the production of propellant charge powders
US4018637A (en) * 1975-02-20 1977-04-19 Olin Corporation Nitrocellulose lacquer with surfactant
US4014719A (en) 1975-10-23 1977-03-29 The United States Of America As Represented By The Secretary Of The Army Flexible explosive composition comprising particulate RDX, HMX or PETN and a nitrostarch binder plasticized with TEGDN or TMETN
US4659402A (en) 1977-12-14 1987-04-21 Hercules Incorporated Cross-linked double base propellant having improved low temperature mechanical properties
US5468311A (en) 1979-03-05 1995-11-21 Hercules Incorporated Binder system for crosslinked double base propellant
US4243442A (en) 1979-05-14 1981-01-06 The United States Of America As Represented By The Secretary Of The Navy Pre-solution preparation of double base propellant binder
US4462848A (en) * 1979-12-28 1984-07-31 Hercules Incorporated Slurry casting method for double base propellants
US4420350A (en) 1980-06-02 1983-12-13 The United States Of America As Represented By The Secretary Of The Navy Doublebase ballistic modifiers
JPS5747789A (en) 1980-09-01 1982-03-18 Nippon Oils & Fats Co Ltd Sheet-like gunpowder, manufacture and use
DE3242301A1 (en) * 1982-11-16 1984-05-17 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V., 8000 München METHOD AND DEVICE FOR THE PRODUCTION OF SINGLE OR MULTI-BASED POWDER CHARGING POWDER
US4477297A (en) 1983-02-28 1984-10-16 Hercules Incorporated Manufacture of gel free nitrocellulose lacquers
GB2152920B (en) 1983-08-12 1987-06-24 Secr Defence Propellant composition
US4841863A (en) 1985-04-19 1989-06-27 Olin Corporation Saboted, light armour penetrator round with improved powder mix
FR2588551B1 (en) 1985-10-14 1987-11-20 Poudres & Explosifs Ste Nale PROCESS FOR PRODUCING A DOUBLE-BASED PROPULSIVE COMPOSITION WITH LOW FLAME LIGHT EMISSION, AND PROPULSIVE COMPOSITION THUS OBTAINED
US4694753A (en) * 1986-02-26 1987-09-22 Olin Corporation Continuous production of low density base grain with a salt-free liquor
FR2604996B1 (en) 1986-10-10 1994-05-06 Poudres Explosifs Ste Nale SINGLE-BASED AGING-RESISTANT POWDER, MANUFACTURING METHOD AND APPLICATION TO GAS GENERATORS
GB8625904D0 (en) * 1986-10-29 1998-11-04 Royal Ordnance Plc Gun propellants
FR2621911B1 (en) * 1987-10-19 1990-02-02 Poudres & Explosifs Ste Nale PROPULSIVE POWDER BASED ON NITROCELLULOSE AND DINITROGLYCOLURILE AND MANUFACTURING METHOD THEREOF
DE3913603C1 (en) * 1989-04-25 1990-03-29 Wnc-Nitrochemie Gmbh, 8261 Aschau, De
AU632562B2 (en) 1989-05-11 1993-01-07 Wnc-Nitrochemie Gmbh Process and device for producing a tribasic propellent powder
US4950342A (en) 1989-09-05 1990-08-21 Olin Corporation Polycaprolactone-deterred nitrocellulose propellant compositions and method
US4909868A (en) 1989-10-16 1990-03-20 The United States Of America As Represented By The Secretary Of The Army Extraction and recovery of plasticizers from solid propellants and munitions
US5218166A (en) 1991-09-20 1993-06-08 Mei Corporation Modified nitrocellulose based propellant composition
US5125684A (en) 1991-10-15 1992-06-30 Hercules Incorporated Extrudable gas generating propellants, method and apparatus
US5540794A (en) 1992-05-11 1996-07-30 Thiokol Corporation Energetic binder and thermoplastic elastomer-based low vulnerability ammunition gun propellants with improved mechanical properties
US5524544A (en) 1994-07-21 1996-06-11 Olin Corporation Nitrocellulose propellant containing a cellulosic burn rate modifier
US5507891A (en) * 1995-08-11 1996-04-16 Alliant Techsystems Inc. Propellant composition for automotive safety applications
US5821449A (en) 1995-09-28 1998-10-13 Alliant Techsystems Inc. Propellant grain geometry for controlling ullage and increasing flame permeability

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090223611A1 (en) * 2006-02-09 2009-09-10 General Dynamics Ordnance And Tactical Systems- Canada Valleyfield Inc. Black Powder Substitutes for Small Caliber Firearms
US8133335B2 (en) * 2006-02-09 2012-03-13 Mathieu Racette Black powder substitutes for small caliber firearms
US20120138200A1 (en) * 2006-02-09 2012-06-07 Mathieu Racette Black Powder Substitutes for Small Caliber Firearms
US8257522B2 (en) * 2006-02-09 2012-09-04 Mathieu Racette Black powder substitutes for small caliber firearms
US8597444B1 (en) * 2007-05-23 2013-12-03 The United States Of America As Represented By The Secretary Of The Army Foamed celluloid combustible material
US8778104B1 (en) * 2008-04-22 2014-07-15 The United States Of America As Represented By The Secretary Of The Navy Insensitive gun propellant, ammunition round assembly, armament system, and related methods
US20150284301A1 (en) * 2013-08-16 2015-10-08 General Dynamics Ordnance And Tactical Systems - Canada Valleyfield Inc. Method of manufacturing multi-layered propellant grains
US10843979B2 (en) * 2013-08-16 2020-11-24 General Dynamics Ordnance and Tactical Systems—Canada Valleyfield Inc. Method of manufacturing multi-layered propellant grains
RU2627408C1 (en) * 2016-07-04 2017-08-08 Федеральное казенное предприятие "Государственный научно-исследовательский институт химических продуктов" (ФКП "ГосНИИХП") Method of producing coarse pellet powder

Also Published As

Publication number Publication date
DK1031547T3 (en) 2005-10-10
EP1031547B1 (en) 2005-06-29
EP1031547A1 (en) 2000-08-30
DE60021001T2 (en) 2006-05-11
DE60021001D1 (en) 2005-08-04
ES2244368T3 (en) 2005-12-16
US6444062B2 (en) 2002-09-03
PT1031547E (en) 2005-11-30
ATE298736T1 (en) 2005-07-15

Similar Documents

Publication Publication Date Title
US6444062B2 (en) Perforated propellant and method of manufacturing same
US3545333A (en) Methods of manufacturing caseless ammunition for air ignition systems
US3897733A (en) High bulk density extruded propellant for small arms cartridges
EP1857429B1 (en) Propulsive means for accelerating projectiles
EP3044191B1 (en) Burn rate modifier
US4326901A (en) Fragmentable charges of propelland powder coated with polyvinyl nitrate, and the process for their manufacture
US3442213A (en) Propellant charge for small arms ammunition
US3954062A (en) Caseless propellant charges
EP2756259B1 (en) Nitroglycerine-free multi-perforated high-performing propellant system
AU2014328459A1 (en) Burn rate modifier
DE3744680C2 (en) High-energy materials and their use
EP1164116B1 (en) Process for producing a functional high-energy material
EP3317606B1 (en) Propellant charge system for artillery shells
US3037247A (en) Process for colloiding nitrocellulose
US20210171415A1 (en) Propellant charge
WO2003084900A1 (en) Method for production of nitrocellulose base for consolidated charges and consolidated propellant charge based thereon
CA2922845C (en) Burn rate modifier
EP1364931B1 (en) Gun propellant powders of high power and reduced erosive action
KR20200051574A (en) Composition for single base propulsion powder for ammunition and ammunition provided with such composition

Legal Events

Date Code Title Description
AS Assignment

Owner name: GENERAL DYNAMICS ORDNANCE & TACTICAL SYSTEMS, INC.

Free format text: CHANGE OF NAME;ASSIGNOR:PRIMEX TECHNOLOGIES, INC.;REEL/FRAME:013070/0155

Effective date: 20010127

AS Assignment

Owner name: AFFIBODY AB, SWEDEN

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:NYGREN, PER-AKE;UHLEN, MATHIAS;REEL/FRAME:013152/0516

Effective date: 20020529

STCF Information on status: patent grant

Free format text: PATENTED CASE

FPAY Fee payment

Year of fee payment: 4

FPAY Fee payment

Year of fee payment: 8

FPAY Fee payment

Year of fee payment: 12