US3725516A - Mixing process and extrusion of solid propellants - Google Patents
Mixing process and extrusion of solid propellants Download PDFInfo
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- US3725516A US3725516A US00738721A US3725516DA US3725516A US 3725516 A US3725516 A US 3725516A US 00738721 A US00738721 A US 00738721A US 3725516D A US3725516D A US 3725516DA US 3725516 A US3725516 A US 3725516A
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- 238000000034 method Methods 0.000 title claims description 14
- 239000004449 solid propellant Substances 0.000 title abstract description 10
- 238000001125 extrusion Methods 0.000 title description 4
- 238000002156 mixing Methods 0.000 title description 3
- 239000000203 mixture Substances 0.000 claims abstract description 43
- GDDNTTHUKVNJRA-UHFFFAOYSA-N 3-bromo-3,3-difluoroprop-1-ene Chemical compound FC(F)(Br)C=C GDDNTTHUKVNJRA-UHFFFAOYSA-N 0.000 claims abstract description 15
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 14
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000007800 oxidant agent Substances 0.000 claims abstract description 14
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims abstract description 13
- 229910052726 zirconium Inorganic materials 0.000 claims abstract description 13
- 229910052790 beryllium Inorganic materials 0.000 claims abstract description 10
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 claims abstract description 10
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229910052749 magnesium Inorganic materials 0.000 claims abstract description 6
- 239000011777 magnesium Substances 0.000 claims abstract description 6
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 claims abstract description 5
- AXZAYXJCENRGIM-UHFFFAOYSA-J dipotassium;tetrabromoplatinum(2-) Chemical compound [K+].[K+].[Br-].[Br-].[Br-].[Br-].[Pt+2] AXZAYXJCENRGIM-UHFFFAOYSA-J 0.000 claims abstract description 5
- 229910001487 potassium perchlorate Inorganic materials 0.000 claims abstract description 5
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 24
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 18
- 239000000446 fuel Substances 0.000 claims description 15
- 239000007787 solid Substances 0.000 claims description 9
- 238000003756 stirring Methods 0.000 claims description 9
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 7
- 229910052796 boron Inorganic materials 0.000 claims description 7
- 239000007788 liquid Substances 0.000 claims description 5
- 238000007605 air drying Methods 0.000 claims description 3
- 238000005406 washing Methods 0.000 claims description 3
- 238000001914 filtration Methods 0.000 claims description 2
- 239000008240 homogeneous mixture Substances 0.000 claims description 2
- 229920002449 FKM Polymers 0.000 abstract description 10
- 239000000843 powder Substances 0.000 abstract description 10
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 abstract description 7
- 229920001577 copolymer Polymers 0.000 abstract description 7
- 229910052751 metal Inorganic materials 0.000 abstract description 5
- 239000002184 metal Substances 0.000 abstract description 5
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 abstract description 4
- 239000003380 propellant Substances 0.000 description 26
- 239000011230 binding agent Substances 0.000 description 9
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 9
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 description 5
- PXIPVTKHYLBLMZ-UHFFFAOYSA-N Sodium azide Chemical compound [Na+].[N-]=[N+]=[N-] PXIPVTKHYLBLMZ-UHFFFAOYSA-N 0.000 description 4
- 229920001971 elastomer Polymers 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 229920004459 Kel-F® PCTFE Polymers 0.000 description 3
- 238000007906 compression Methods 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 239000000806 elastomer Substances 0.000 description 3
- 150000004678 hydrides Chemical class 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- 238000005054 agglomeration Methods 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- XYODKMYYACGWBN-UHFFFAOYSA-N aminoazanium;nitroformate Chemical compound [NH3+]N.[O-]C(=O)[N+]([O-])=O XYODKMYYACGWBN-UHFFFAOYSA-N 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- MFEVGQHCNVXMER-UHFFFAOYSA-L 1,3,2$l^{2}-dioxaplumbetan-4-one Chemical compound [Pb+2].[O-]C([O-])=O MFEVGQHCNVXMER-UHFFFAOYSA-L 0.000 description 1
- JXSRRBVHLUJJFC-UHFFFAOYSA-N 7-amino-2-methylsulfanyl-[1,2,4]triazolo[1,5-a]pyrimidine-6-carbonitrile Chemical compound N1=CC(C#N)=C(N)N2N=C(SC)N=C21 JXSRRBVHLUJJFC-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 1
- 239000005751 Copper oxide Substances 0.000 description 1
- 229910000003 Lead carbonate Inorganic materials 0.000 description 1
- 229910007727 Zr V Inorganic materials 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910001485 alkali metal perchlorate Inorganic materials 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- CNVULGHYDPMIHD-UHFFFAOYSA-L bis[(2-hydroxybenzoyl)oxy]lead Chemical compound [Pb+2].OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O CNVULGHYDPMIHD-UHFFFAOYSA-L 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- JGDFBJMWFLXCLJ-UHFFFAOYSA-N copper chromite Chemical compound [Cu]=O.[Cu]=O.O=[Cr]O[Cr]=O JGDFBJMWFLXCLJ-UHFFFAOYSA-N 0.000 description 1
- 229910000431 copper oxide Inorganic materials 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical compound [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000011031 large-scale manufacturing process Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical class OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- -1 pyrotechnics Substances 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B21/00—Apparatus or methods for working-up explosives, e.g. forming, cutting, drying
- C06B21/0008—Compounding the ingredient
- C06B21/0025—Compounding the ingredient the ingredient being a polymer bonded explosive or thermic component
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B45/00—Compositions or products which are defined by structure or arrangement of component of product
- C06B45/04—Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive
- C06B45/06—Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive the solid solution or matrix containing an organic component
- C06B45/10—Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive the solid solution or matrix containing an organic component the organic component containing a resin
Definitions
- ABSTRACT An improved extrudable, high energy solid propellant composition consisting essentially of the copolymer of vinylidene fluoride and perfluoropropylene (Viton), an inorganic oxidizer such as ammonium perchlorate, potassium perchlorate or ammonium nitrate, and a metal powder such as aluminum, beryllium, magnesium or zirconium.
- This composition is extrudable into any suitable shape and has a very high percentage theoretical maximum density so as to be practical for utilization in rocket motors for propulsion.
- the present invention relates to an improved extrudable, high energy, high density solid propellant and to the method of preparation thereof.
- propellants with a high delivered density-impulse, high temperature stability and good safety characteristics.
- a propellant of this kind finds greatest use in the system where the propellant burnout mass is very large compared to the propellant volume.
- variations in the properties are required for a specific application, variations in the formulation are needed.
- Propellants presently available have density specific impulse values on the order of 430 470 g-sec/cc.
- the achievement of high density in a composite propellant is controlled by the density and generally the particle size of the ingredients and ultimately the method of fabrication which is limited often by safety features of the processing system. Harsh working of the material may cause ignition.
- the present invention attains a very high theoretical density impulse of a value between 490 and 622 gsec/cc which is a considerable increase over prior propellant compositions. Physical properties are I changed; for instance, tensile strength is increased.
- Burning rate modifiers can be added to a basic composition in order to improve ballistic properties of the composition.
- the general purpose of this invention is to produce a basic family of dense propellants which are extrudable or can be compression molded and which have suitable impulses that increased range results from their use in volume limited boost type application.
- the present invention is for an extrudable, high density solid propellant composition and its method of preparation.
- the composition consists essentially of a fluorocarbon binder, such as a copolymer of vinylidene fluoride and perfluoropropene (Viton) or a copolymer of vinylidene fluoride and trifluorochloroethylene (Kel-F elastomer), in the range of from to 35 percent; elemental fuels and their hydrides or mixtures thereof, selected from the group consisting of aluminum, boron, zirconium, beryllium, titanium, magand metal powder thereby forming a suspension.
- a fluorocarbon binder such as a copolymer of vinylidene fluoride and perfluoropropene (Viton) or a copolymer of vinylidene fluoride and trifluorochloroethylene (Kel-F elastomer
- the suspension is then washed with a quantity of a precipitant for the fluorocarbon, in this instance hexane.
- a precipitant for the fluorocarbon in this instance hexane.
- the solid is permitted to settle and the liquid is decanted off.
- the solid is washed again with hexane after which the liquid is decanted off, the solid filtered and air dried or oven dried.
- the powder resulting is compression molded or extruded into the desired shape.
- the object of this method to produce an extrudable, high density solid propellant material which will have greater boost velocity than existing propellants.
- a product which is relatively safe to handle is formed and the process is amenable to large scale production of propellants, pyrotechnics, and explosive materials such as high energy, high density molding powders which can be molded or extruded.
- FIG. 1 is a graph showing the theoretical impulse as a function of the basic composition
- FIG. 2 is a graph showing the theoretical impulse as a function of a zirconium modified basic composition
- FIG. 3 is another graph showing the theoretical impulse as a fimction of a beryllium modified composition
- FIG. 4 is yet another graph showing the theoretical impulse as a function of another modified basic composition.
- FIG. 5 is a graphic comparison of the boost velocities of fluorocarbon bound propellants with propellants containing conventional binders.
- compositions were studied, extruded, or pressed and fired.
- This invention is illustrated, but not limited, by the following basic composition consisting essentially of a fluorocarbon binder, such as a copolymer of vinylidene fluoride and perfluoropropene (Viton) and a copolymer of vinylidene fluoride and trifluorochloroethylene (Kel-F elastomer), in the range of from 10 to 35 percent; elemental fuels and their hydrides or mixtures thereof, such as aluminum, boron, zirconium, beryllium, titanium, magnesium, and their hydrides, in the range of from about 5 to percent; and an oxidizer, generally an inorganic oxidizer such as ammonium or alkali metal perchlorate in the range of from about 25 to percent.
- a fluorocarbon binder such as a copolymer of vinylidene fluoride and perfluoropropene (Viton) and a copo
- the density of boron is 2.34 g/cc, but the density of lead is 11.4 g/cc, and that of tungsten is 19.32 glcc.
- Oxidizers such as ammonium or alkali perchlorates and nitrates are interchangeable as far as processing is concerned. Calculations indicate that oxidizers such as hydrazine nitroformate will theoretically provide even better performance.
- Modified Composition A Constituents Percent by weight Viton l 8.5 Sodium azide 9.1 Ammonium perchlorate 54.6 Aluminum 1 8. l 5
- the sodium azide acts as a catalyst. Burn rate results of the extruded strands were as follows:
- the process by which the present invention is made uses a resin kettle with a fast propeller stirrer and a stiff rubber baffling device to prevent vortex formation.
- a stainless steel drum may be used to make larger batches.
- the required quantity of binder is placed in a container and dissolved in acetone or other suitable solvents such as methylethyl ketone and ethyl acetate. Approximately 25 cc of acetone per gram of Viton or Kel-F elastomer is used. Into this solution at room temperature are stirred the dry solid ingredients, the metal powder and oxidizer.
- the remaining wet solid receives a second hexane wash after which it is decanted off, filtered and air dried or oven dried at C. In this manner agglomeration is avoided. If a finer powder is desired, the second hexane wash may be decanted off and the wet solid screened. The powder after air drying and vacuum drying is compression molded or extruded into the desired shapes. The propellant surfaces not to be burned are inhibited prior to motor firmg.
- FIG. 1 is a graphic view of the theoretical specific impulse as a function of the basic formulation, as above set out, consisting essentially of Viton, aluminum, and ammonium perchlorate.
- FIG. 2 illustrates the theoretical specific impulse as a function of the composition wherein the basic formulation was modified by using zirconium as the elemental fuel in place of aluminum.
- FIG. 3 the theoretical specific impulse as a function of the composition is shown in which beryllium was the elemental fuel used.
- FIG. 4 illustrates the theoretical impulse as a function of the composition wherein hydrazine nitroformate is the oxidizer with a fluorocarbon binder and the fuel, beryllium.
- FIG. 1 is a graphic view of the theoretical specific impulse as a function of the basic formulation, as above set out, consisting essentially of Viton, aluminum, and ammonium perchlorate.
- FIG. 2 illustrates the theoretical specific impulse as a function of the composition wherein the basic formulation was modified by using zirconium as the elemental fuel in
- Y IKEIZE 1 11 Composition (percent Meas- Percent by weight) Composition ured theoretical Measby analysis, denmaximum ured Viton AP Al Zr V/AP/Al/Zr sity density 1.,
- V Viton The invention described herein may be manufac- 5 tured and used by or for the Government of the United States of America for governmental purposes without the payment of any royalties thereon or therefor.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dispersion Chemistry (AREA)
- Molecular Biology (AREA)
- Crystallography & Structural Chemistry (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
Abstract
An improved extrudable, high energy solid propellant composition consisting essentially of the copolymer of vinylidene fluoride and perfluoropropylene (Viton), an inorganic oxidizer such as ammonium perchlorate, potassium perchlorate or ammonium nitrate, and a metal powder such as aluminum, beryllium, magnesium or zirconium. This composition is extrudable into any suitable shape and has a very high percentage theoretical maximum density so as to be practical for utilization in rocket motors for propulsion.
Description
United States Patent 1 1 Kaufman MIXING PROCESS AND EXTRUSION v0F SOLID PROPELLANTS Inventor: Martin H. Kaufman, China Lake,
Calif.
Assignee: The United .States of America as represented by the Secretary of the Navy Filed: June 11, 1968 Appl. No.: 738,721
Related U.S. Application Data Continuation of Ser. No. 361,612, April 17, 1964.
U.S. Cl. ..264/3 B, 149/22, 149/40, 149/41, 149/42, 149/43, 149/44 Int. Cl. ..'.....C06b 21/02 Field of Search ..264/3; 149/22, 60, 40, 42, 149/43, 44, 41, 76, 85,19, 20
[56] References Cited UNITED STATES PATENTS 3,155,749 11/1964 Rossen et al. ..264/3 3,351,505 11/1967 Shapiro et a1. 3,431,154 3/1969 Kelly et al ..149/44 X Primary Examiner-Stephen J. Lechert, Jr. Attorney-George J. Rubens and Roy Miller [57] ABSTRACT An improved extrudable, high energy solid propellant composition consisting essentially of the copolymer of vinylidene fluoride and perfluoropropylene (Viton), an inorganic oxidizer such as ammonium perchlorate, potassium perchlorate or ammonium nitrate, and a metal powder such as aluminum, beryllium, magnesium or zirconium. This composition is extrudable into any suitable shape and has a very high percentage theoretical maximum density so as to be practical for utilization in rocket motors for propulsion.
4 Claims, No Drawings MIXING PROCESS AND EXTRUSION OF SOLID PROPELLANTS REFERENCE TO RELATED APPLICATION This invention is a continuation of US. Pat. application Ser. No. 361,612, filed in the U. S. Patent Office on 17 April 1964.
BACKGROUND OF THE INVENTION The present invention relates to an improved extrudable, high energy, high density solid propellant and to the method of preparation thereof.
Those concerned with the development of solid propellants have long known and recognized the need for a propellant with a high delivered density-impulse, high temperature stability and good safety characteristics. A propellant of this kind finds greatest use in the system where the propellant burnout mass is very large compared to the propellant volume. As variations in the properties are required for a specific application, variations in the formulation are needed. Propellants presently available have density specific impulse values on the order of 430 470 g-sec/cc. The achievement of high density in a composite propellant is controlled by the density and generally the particle size of the ingredients and ultimately the method of fabrication which is limited often by safety features of the processing system. Harsh working of the material may cause ignition.
The present invention attains a very high theoretical density impulse of a value between 490 and 622 gsec/cc which is a considerable increase over prior propellant compositions. Physical properties are I changed; for instance, tensile strength is increased.
Burning rate modifiers can be added to a basic composition in order to improve ballistic properties of the composition. The general purpose of this invention, therefore, is to produce a basic family of dense propellants which are extrudable or can be compression molded and which have suitable impulses that increased range results from their use in volume limited boost type application.
SUMMARY OF THE INVENTION The present invention is for an extrudable, high density solid propellant composition and its method of preparation. The composition consists essentially of a fluorocarbon binder, such as a copolymer of vinylidene fluoride and perfluoropropene (Viton) or a copolymer of vinylidene fluoride and trifluorochloroethylene (Kel-F elastomer), in the range of from to 35 percent; elemental fuels and their hydrides or mixtures thereof, selected from the group consisting of aluminum, boron, zirconium, beryllium, titanium, magand metal powder thereby forming a suspension. The suspension is then washed with a quantity of a precipitant for the fluorocarbon, in this instance hexane. The solid is permitted to settle and the liquid is decanted off. The solid is washed again with hexane after which the liquid is decanted off, the solid filtered and air dried or oven dried. The powder resulting is compression molded or extruded into the desired shape. The object of this method to produce an extrudable, high density solid propellant material which will have greater boost velocity than existing propellants. A product which is relatively safe to handle is formed and the process is amenable to large scale production of propellants, pyrotechnics, and explosive materials such as high energy, high density molding powders which can be molded or extruded.
Other objects and many attendant advantages of this invention will be readily appreciated as the same become better understood by reference to the following detailed description when considered in connection with the accompanying graphs.
BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a graph showing the theoretical impulse as a function of the basic composition;
FIG. 2 is a graph showing the theoretical impulse as a function of a zirconium modified basic composition;
FIG. 3 is another graph showing the theoretical impulse as a fimction of a beryllium modified composition;
FIG. 4 is yet another graph showing the theoretical impulse as a function of another modified basic composition; and
FIG. 5 is a graphic comparison of the boost velocities of fluorocarbon bound propellants with propellants containing conventional binders.
DESCRIPTION OF THE INVENTION In the present invention many compositions were studied, extruded, or pressed and fired. This invention is illustrated, but not limited, by the following basic composition consisting essentially of a fluorocarbon binder, such as a copolymer of vinylidene fluoride and perfluoropropene (Viton) and a copolymer of vinylidene fluoride and trifluorochloroethylene (Kel-F elastomer), in the range of from 10 to 35 percent; elemental fuels and their hydrides or mixtures thereof, such as aluminum, boron, zirconium, beryllium, titanium, magnesium, and their hydrides, in the range of from about 5 to percent; and an oxidizer, generally an inorganic oxidizer such as ammonium or alkali metal perchlorate in the range of from about 25 to percent.
In the use of very dense metals, less binder is required on a weight basis as the fuel volumes get smaller. For example, the density of boron is 2.34 g/cc, but the density of lead is 11.4 g/cc, and that of tungsten is 19.32 glcc.
Oxidizers such as ammonium or alkali perchlorates and nitrates are interchangeable as far as processing is concerned. Calculations indicate that oxidizers such as hydrazine nitroformate will theoretically provide even better performance.
The following basic composition was modified as hereinafter described.
Basic Composition Constituents Percent by weight Ammonium perchlorate 59 Aluminum 21 Viton A 20 The addition of various fuel mixtures to the above extrudable basic composition provided changes in burning rates which are shown in the-following table. For example, the addition of copper, iron, boron, chromium, zirconium, or their derivatives at the percent level in the basic composition showed significant burning rate changes:
TABLE I Burning Rate (in/sec.)
1000 psi 4000 psi Basic fonnulation 0.47 1.07
Extruded basic formulation modified by addition of Ferrocene 0.70 1.5 Copper 0.54 1.1 Boron 0.72 1.65 Chromium 0.5 1.1 Copper Chromite 0.64 1.5 Copper Stearate 0.56 1.2 Copper Oxide 0.56 1.2 Lead Salicylate 0.52 1.0 Lead Resorcylate 1.10 Titanium Dioxide 0.58 1.37 Zirconium Boride 0.53 1.35 Lead Carbonate 0.52 1.35
Mixtures of aluminum and zirconium as high energy, high density ingredients also produced significant changes in the burning rate of the extruded basic composition as shown in the following table:
TABLE 11 Burning Rate (in/sec.)
Composition Burning Rate (Percent by Weight) (psi) Viton AN Al KP Zr Tef IOOOAP 4000 15 45 20 15 5 0.60 1.35 15 45 20 20 0.77 1.95 30 20 50 0.47 1.22 20 80 0.40 0.82 25 75 0.40 0.84 15 85 0.06 0.15 15 75 0.45 0.92 16 50 20 10 4 0.63 1.35 18.5 45 16.5 16.5 3.5 0.53 1.25
AP ammonium perchlorate AN ammonium nitrate A1 aluminum KP potassium perchlorate Zr zirconium Other modifications of the basic composition which showed significant changes in the burning are as follows:
Modified Composition A Constituents Percent by weight Viton l 8.5 Sodium azide 9.1 Ammonium perchlorate 54.6 Aluminum 1 8. l 5
The sodium azide acts as a catalyst. Burn rate results of the extruded strands were as follows:
0.37 in/sec at 1000 psi 0.78 in/sec at 4000 psi Modified Composition B Constituents Percent by weight Viton 25 Magnesium 20 Ammonium perchlorate Burn rate results of the extruded propellant were as follows:
0.54 in/sec at 1000 psi 1.07 in/sec at 4000 psi The process by which the present invention is made uses a resin kettle with a fast propeller stirrer and a stiff rubber baffling device to prevent vortex formation. A stainless steel drum may be used to make larger batches. The required quantity of binder is placed in a container and dissolved in acetone or other suitable solvents such as methylethyl ketone and ethyl acetate. Approximately 25 cc of acetone per gram of Viton or Kel-F elastomer is used. Into this solution at room temperature are stirred the dry solid ingredients, the metal powder and oxidizer. After about 5 minutes of stirring the suspension a quantity of a precipitant for the fluorocarbon, about two and one-half times by volume that of fluorocarbon solvent is added with stirring. l-lexane was used in this instance. Other hydrocarbons such as petroleum ether may be used. After an additional 5 minutes of stirring, the solid is permitted to settle and the liquid is decanted off. Care must be taken at this point to prevent complete decantation, especially prior to the first washing. Residual solvent will permit easy agglomeration of the powder at this stage if most of the hydrocarbon evaporates off. The latter is detrimental to the preparation of a free-flowing molding powder which is suitable for extrusion. The remaining wet solid receives a second hexane wash after which it is decanted off, filtered and air dried or oven dried at C. In this manner agglomeration is avoided. If a finer powder is desired, the second hexane wash may be decanted off and the wet solid screened. The powder after air drying and vacuum drying is compression molded or extruded into the desired shapes. The propellant surfaces not to be burned are inhibited prior to motor firmg.
Referring now to the drawings, FIG. 1 is a graphic view of the theoretical specific impulse as a function of the basic formulation, as above set out, consisting essentially of Viton, aluminum, and ammonium perchlorate. FIG. 2 illustrates the theoretical specific impulse as a function of the composition wherein the basic formulation was modified by using zirconium as the elemental fuel in place of aluminum. In FIG. 3 the theoretical specific impulse as a function of the composition is shown in which beryllium was the elemental fuel used. FIG. 4 illustrates the theoretical impulse as a function of the composition wherein hydrazine nitroformate is the oxidizer with a fluorocarbon binder and the fuel, beryllium. FIG. 5 compares the boost velocities of fluorocarbon bound propellants with propellants bound with conventional binders such as polyurethanes and polyhydrocarbons. These conventional binders are designated by the symbol Cl-l The performance of an ideal rocket, i.e., no pressure thrust, drag or gravitation or what may be termed a gravitationless vacuum is given by The logarithmic relation makes V very dependent on a mass ratio. If the rocket were all propellant the V would theoretically be infinite. Now if m (mass of rocket at burnout) m, m,, and since,
m, density of propellant, p, x volume of propellant,
so that BO 8Dg [Pp 50/ vl) wherein V Velocity of rocket at propellant burnout C,,,, Time average exhaust velocity (cm/sec) 1,,
m, Total rocket mass at time zero m, Total propellant mass at time zero t Time I Specific impulse g =Gravity Since the mass of a rocket without propellant, and the volume to be occupied by the propellant generally are both fixed by design, the ratio "130/ V, (very often called the mass to volume ratio) is independent of propellant characteristics and actually characterizes the rocket or missile.
In FIG. it is shown that the boost velocity (V of fluorocarbon bound propellant is considerably better than the conventional binders.
The following table shows test results of several batches of propellants prepared in accordance with the present invention.
Y IKEIZE 1 11 Composition (percent Meas- Percent by weight) Composition ured theoretical Measby analysis, denmaximum ured Viton AP Al Zr V/AP/Al/Zr sity density 1.,
V Viton The invention described herein may be manufac- 5 tured and used by or for the Government of the United States of America for governmental purposes without the payment of any royalties thereon or therefor.
What is claimed is:
l. The process for preparing an extrudable, high energy solid propellant comprising the steps of l. dissolving a copolymer of vinylidene fluoride and perfiuoropropylene in acetone to form a solution;
2. adding while stirring weighed quantities of a dry oxidizer selected from the group consisting of ammonium perchlorate, ammonium nitrate, potassium perchlorate and mixtures thereof and a fuel selected from the group consisting of aluminum, boron, beryllium, magnesium, and zirconium to form a homogeneous mixture;
3. adding to said mixture while stirring a volume of hexane about three times the volume of said acetone; permitting said acetone and mixture to stan without stirring until all the solids settle;
5. decanting off substantially all the liquid leaving a residue;
6. washing the residue with hexane of about three times the volume of acetone;
7. filtering out said residue;
8. air drying the residue; and
9. extruding said residue.
2. The process as defined in claim 1 wherein the oxidizer is ammonium perchlorate and the fuel is aluminum.
3. The process as defined in claim 1 wherein the oxidizer is ammonium perchlorate and the fuel is zirconi- 4. The process as defined in claim 1 wherein the oxidizer is ammonium perchlorate and the fuel is berylli-
Claims (11)
- 2. adding while stirring weighed quantities of a dry oxidizer selected from the group cOnsisting of ammonium perchlorate, ammonium nitrate, potassium perchlorate and mixtures thereof and a fuel selected from the group consisting of aluminum, boron, beryllium, magnesium, and zirconium to form a homogeneous mixture;
- 2. The process as defined in claim 1 wherein the oxidizer is ammonium perchlorate and the fuel is aluminum.
- 3. The process as defined in claim 1 wherein the oxidizer is ammonium perchlorate and the fuel is zirconium.
- 3. adding to said mixture while stirring a volume of hexane about three times the volume of said acetone;
- 4. permitting said acetone and mixture to stand without stirring until all the solids settle;
- 4. The process as defined in claim 1 wherein the oxidizer is ammonium perchlorate and the fuel is beryllium.
- 5. decanting off substantially all the liquid leaving a residue;
- 6. washing the residue with hexane of about three times the volume of acetone;
- 7. filtering out said residue;
- 8. air drying the residue; and
- 9. extruding said residue.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US36161264A | 1964-04-17 | 1964-04-17 | |
| US73872168A | 1968-06-11 | 1968-06-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3725516A true US3725516A (en) | 1973-04-03 |
Family
ID=27001357
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US00738721A Expired - Lifetime US3725516A (en) | 1964-04-17 | 1968-06-11 | Mixing process and extrusion of solid propellants |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3725516A (en) |
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3876478A (en) * | 1972-12-18 | 1975-04-08 | Us Navy | Light sensitive explosive mixture |
| WO1986002347A1 (en) * | 1984-10-10 | 1986-04-24 | Kurtz Earl F | Explosive composition and method |
| US4964929A (en) * | 1986-11-27 | 1990-10-23 | Hoffmann-La Roche Inc. | Preparation of explosives containing degradation products of ascorbic or isoascorbic acid |
| US4997496A (en) * | 1989-06-13 | 1991-03-05 | Hoffmann-La Roche Inc. | Explosive and propellant composition and method |
| US5180452A (en) * | 1990-12-27 | 1993-01-19 | Thiokol Corporation | Solid propellant formualtions producing acid neutralizing exhaust |
| EP0727403A1 (en) * | 1995-02-09 | 1996-08-21 | State Of Israel, Ministry Of Defence, Rafael-Armaments Development Authority | Inverse hybrid propulsion system |
| US6024811A (en) * | 1997-12-22 | 2000-02-15 | Societe Nationale Des Poudres Et Explosifs | Pyrotechnic composition generating clean gases with low levels of nitrogen oxides, and pellets of such a composition |
| US6136111A (en) * | 1996-05-30 | 2000-10-24 | Quantic Industries, Inc. | Combustible composition for use in vehicle safety systems |
| US6679960B2 (en) | 2001-04-25 | 2004-01-20 | Lockheed Martin Corporation | Energy dense explosives |
| US20040226638A1 (en) * | 2003-05-16 | 2004-11-18 | Posson Philip L. | Energetics binder of fluoroelastomer or other latex |
| WO2011154089A1 (en) * | 2010-06-08 | 2011-12-15 | Rheinmetall Waffe Munition Gmbh | Method for producing and using an explosive substance mixture containing fuel |
| US10415938B2 (en) | 2017-01-16 | 2019-09-17 | Spectre Enterprises, Inc. | Propellant |
| US11112222B2 (en) | 2019-01-21 | 2021-09-07 | Spectre Materials Sciences, Inc. | Propellant with pattern-controlled burn rate |
| US11650037B2 (en) | 2021-02-16 | 2023-05-16 | Spectre Materials Sciences, Inc. | Primer for firearms and other munitions |
| US12234198B2 (en) | 2020-08-05 | 2025-02-25 | Spectre Enterprises, Inc. | Passivated fuel |
| US12385727B2 (en) | 2023-04-29 | 2025-08-12 | Spectre Primer Technologies, Inc. | Fuzzy interface layer for thermite and primer made from thermite with fuzzy layer |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3155749A (en) * | 1960-05-03 | 1964-11-03 | Atlantic Res Corp | Extrusion process for making propellant grains |
| US3351505A (en) * | 1960-09-01 | 1967-11-07 | Hughes Tool Co | High energy solid propellants containing fluoropolymers and metallic fuels |
| US3431154A (en) * | 1968-07-31 | 1969-03-04 | Canadian Ind | Aqueous slurry explosive composition containing a chlorinated organic compound as sensitizer |
-
1968
- 1968-06-11 US US00738721A patent/US3725516A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3155749A (en) * | 1960-05-03 | 1964-11-03 | Atlantic Res Corp | Extrusion process for making propellant grains |
| US3351505A (en) * | 1960-09-01 | 1967-11-07 | Hughes Tool Co | High energy solid propellants containing fluoropolymers and metallic fuels |
| US3431154A (en) * | 1968-07-31 | 1969-03-04 | Canadian Ind | Aqueous slurry explosive composition containing a chlorinated organic compound as sensitizer |
Cited By (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3876478A (en) * | 1972-12-18 | 1975-04-08 | Us Navy | Light sensitive explosive mixture |
| WO1986002347A1 (en) * | 1984-10-10 | 1986-04-24 | Kurtz Earl F | Explosive composition and method |
| US4964929A (en) * | 1986-11-27 | 1990-10-23 | Hoffmann-La Roche Inc. | Preparation of explosives containing degradation products of ascorbic or isoascorbic acid |
| US4997496A (en) * | 1989-06-13 | 1991-03-05 | Hoffmann-La Roche Inc. | Explosive and propellant composition and method |
| US5180452A (en) * | 1990-12-27 | 1993-01-19 | Thiokol Corporation | Solid propellant formualtions producing acid neutralizing exhaust |
| EP0727403A1 (en) * | 1995-02-09 | 1996-08-21 | State Of Israel, Ministry Of Defence, Rafael-Armaments Development Authority | Inverse hybrid propulsion system |
| US6136111A (en) * | 1996-05-30 | 2000-10-24 | Quantic Industries, Inc. | Combustible composition for use in vehicle safety systems |
| US6024811A (en) * | 1997-12-22 | 2000-02-15 | Societe Nationale Des Poudres Et Explosifs | Pyrotechnic composition generating clean gases with low levels of nitrogen oxides, and pellets of such a composition |
| US6679960B2 (en) | 2001-04-25 | 2004-01-20 | Lockheed Martin Corporation | Energy dense explosives |
| US20040226638A1 (en) * | 2003-05-16 | 2004-11-18 | Posson Philip L. | Energetics binder of fluoroelastomer or other latex |
| US6896751B2 (en) | 2003-05-16 | 2005-05-24 | Universal Propulsion Company, Inc. | Energetics binder of fluoroelastomer or other latex |
| WO2011154089A1 (en) * | 2010-06-08 | 2011-12-15 | Rheinmetall Waffe Munition Gmbh | Method for producing and using an explosive substance mixture containing fuel |
| US10415938B2 (en) | 2017-01-16 | 2019-09-17 | Spectre Enterprises, Inc. | Propellant |
| US11112222B2 (en) | 2019-01-21 | 2021-09-07 | Spectre Materials Sciences, Inc. | Propellant with pattern-controlled burn rate |
| US12234198B2 (en) | 2020-08-05 | 2025-02-25 | Spectre Enterprises, Inc. | Passivated fuel |
| US11650037B2 (en) | 2021-02-16 | 2023-05-16 | Spectre Materials Sciences, Inc. | Primer for firearms and other munitions |
| US12385727B2 (en) | 2023-04-29 | 2025-08-12 | Spectre Primer Technologies, Inc. | Fuzzy interface layer for thermite and primer made from thermite with fuzzy layer |
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