US3876477A - Fluorocarbon solid propellant with burning rate modifier - Google Patents
Fluorocarbon solid propellant with burning rate modifier Download PDFInfo
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- US3876477A US3876477A US491496A US49149665A US3876477A US 3876477 A US3876477 A US 3876477A US 491496 A US491496 A US 491496A US 49149665 A US49149665 A US 49149665A US 3876477 A US3876477 A US 3876477A
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- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B23/00—Compositions characterised by non-explosive or non-thermic constituents
- C06B23/007—Ballistic modifiers, burning rate catalysts, burning rate depressing agents, e.g. for gas generating
-
- 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
- the present invention relates to improved solid propellants.
- a specific aspect relates to solid fluorocarbon propellants containing burning rate modifiers.
- the fluorocarbon family of polymers has developed as excellent binders for composite solid propellants. Because of their high density, thermal stability, water impermeability, compatibility with a wide range of propellant ingredients, and high heat of reaction with metals, the fluorinated binders possess many desirable properties for propellant compositions.
- the propellants prepared with these binders have high structural integrity, long storage life, and good physical properties.
- the present invention provides a composition with increased burning rates, low pressure exponent or low temperature coefficient.
- Another object is to provide a propellant with exceptionally high structural integrity and a long storage life under varying environmental conditions.
- Yet another object is to provide an improved propeI- lant composition which can be produced in large volumes at low cost.
- a propellant comprising up to 60 percent by weight of an oxidizer from 5 to 65 percent by weight of a binder consisting of a mixture of fluorocarbon polymers; up to 30 percent by weight metal fuel; and from 1 to 3 percent by weight chemical modifiers.
- the oxidants which are applicable to the solid propellant of this invention are those oxygen-containing solids which readily give up oxygen and include ammonium, alkali metal and alkaline earth metal salts of nitric, perchloric, and chloric acids, and mixtures thereof.
- Ammonium perchlorate, potassium perchlorate, ammonium nitrate and hydrazine diperchlorate are preferred oxidizers for this invention.
- the fluorocarbon polymers used in the composition consist of polytetrafluoroethylene (hereinafter referred to as Teflon) and a copolymer of vinylidene fluoride and hexafluoropropylene (hereinafter referred to as Viton-A) and mixtures thereof.
- Teflon polytetrafluoroethylene
- Viton-A copolymer of vinylidene fluoride and hexafluoropropylene
- the high energy fuels preferred are aluminum, mag nesium, zirconium, uranium, thorium. beryllium and mixtures thereof. These metals will usually have a particle size within the ranges of l to 100 microns.
- the chemical modifiers preferred for the present composition consist of copper, lead, tin, sodium, ammonium and potassium fluoborates; sodium, potassium, lithium, lead, copper, and calcium fluorides; potassium and ammonium dichromate; lead and zinc stearate; cesium carbonate; potassium and ammonium sulfate; copper chromite; oxides of magnesium, copper and manganese; boron; zinc dust; and carbon black.
- One convenient method, and the presently preferred method, of preparing this composition comprises, first. dissolving the Viton-A in a solvent selected from a lowboiling ketone; acetone was used. The Teflon and other ingredients (fuel, oxidizer and modifier) were then thoroughly mixed into the Viton-A solution to form a uniform slurry or suspension. The slurry was washed for from 5 to 10 minutes with hexane, the volume of hexane being from 1 to 4 times the volume of slurry. By this step the Viton precipitates onto the other solids in the slurry. After the suspension had settled, the supernatant hexane was decanted and the resulting residue was dried under ambient conditions for from 8 to 24 hours. The slurry may be washed with normal hexane 2 or 3 times, as necessary.
- a general formulation for a propellant composition prepared in accordance with the invention is as follows:
- Binder 5 to Viton-A 10 to 15 Teflon 5 to 50 Oxidizer up to 65 Metal Fuel up to 35 Chemical modifier l to 3 Ingredients Percent by weight Binder 5 to Viton-A 10 to 15 Teflon 5 to 50 Oxidizer up to 65 Metal Fuel up to 35 Chemical modifier l to 3
- Binder 5 to Viton-A 10 to 15 Teflon 5 to 50 Oxidizer up to 65 Metal Fuel up to 35 Chemical modifier l to 3 Ingredients Percent by weight Binder 5 to Viton-A 10 to 15 Teflon 5 to 50 Oxidizer up to 65 Metal Fuel up to 35 Chemical modifier l to 3
- the following examples will serve to further illustrate the invention.
- the above ingredients were processed by the shockgel technique described hereinbefore.
- the Viton is available in acetone solution for which an assay should be available.
- the solution should contain a minimum of 8 and a maximum of 22 weight percent Viton. All of the ingredients are added to a slurry pot.
- a volume of hexane equal to 4 times the volume of the Viton solution is placed in a container. While stirring the slurry, hexane is added slowly and mixing continues for about 15 minutes.
- the Viton is precipitated or shock-gelled onto the solids in the slurry.
- the supernatant hexane is siphoned off and an additional volume of fresh hexane, equal to the first volume, is added.
- the supernatant hexane is siphoned off and the resulting composition is collected in a cloth bag and dried in a drying oven for from 8 to 24 hours at approximately F. Some of the material was extruded into strands for burning tests. This composition showed a burning rate at 1000 psi of 0.298-inch per second and a pressure exponent of 0.61.
- the Viton-A is dissolved in acetone. To this solution the Teflon, aluminum, potassium perchlorate and sodium fluoride were added and mixed for about 10 minutes forming a slurry. The slurry was washed with hexane (4 volumes of hexane to 1 volume of Viton solution) for 10 minutes. The resulting mixture was let settle and hexane was siphoned off. The residue was washed with an additional volume of hexane for about 5 minutes. The supernatant hexane was again siphoned off, the composition collected in a cloth bag and dried. This material extrudes well. It showed a burning rate at 2000 psia of 0.63 inch per second and a pressure exponent of 0.53.
- the Viton was dissolved in acetone and all the ingredients were stirred therein for about 10 minutes forming a slurry orsuspension.
- the suspension was dropped into rapidly agitated hexane and stirred for 10 minutes. (About 4 volumes of hexane to one of Viton solution). After letting the composition settle out, the hexane was siphoned off. The composition was washed again with hexane which was decanted and the material was collected and dried. Some of this composition was extruded for burn rate determination.
- EXAMPLE V Ingredients Percent by weight Function Viton-A l5 Binder Teflon l5 Binder Potassium perchlorate 49 Oxidizer Aluminum 18 Fuel Zinc(dust) 2 Modifier Sodium fluoride 1 Modifier These ingredients were processed as those in the previous examples. Burn strands formed from this composition showed a burning rate at 2000 psi of 0.74 inch per second and a pressure exponent of 0.77.
- EXAMPLE VI Ingredients Percent by weight Function Viton-A l5 Binder Teflon l5 Binder Potassium perchlorate 49 Oxidizer Aluminum 18 Fuel Cupric oxide 2 Modifier Sodium fluoride I Modifier Strands of this composition gave a burning rate at 2000 psi of 0.68 inch per second and a pressure exponent of 0.82.
- EXAMPLE VII Ingredients Percent by weight Function Viton-A l5 Binder Teflon l5 Binder Ammonium perchlorate 49 Oxidizer Aluminum 18 Fuel Lead 2 Modifier Sodium fluoride l Modifier Strands were extruded of this composition whiclgave a burning rate at 2000 psi of 0.76 inch per seconc and a pressure exponent of 0.78.
- EXAMPLE Vlll Ingredients Percent by weight Function Teflon 51 Binder Viton-A 15 Binder Magnesium 31 Fuel Cuprie fluoride 3 Modifier The ingredients were processed in accordance witl the prior samples and strands were extruded for burn ing rate determination.
- a solid propellant composition consisting essentially of the following:
- a solid propellant composition consisting essentially of the following:
- a solid propellant composition consisting essentially of .the following:
- a solid propellant composition consisting essentially of the following:
- a solid propellant composition consisting essentially of the following:
- a solid propellant composition consisting essentially of the following:
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
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Abstract
Solid fluorocarbon propellant compositions containing burning rate modifi which have high structural integrity and a long storage life under varying environmental conditions.
Description
Eldridge et al.
FLUOROCARBON SOLID PROPELLANT WlTl-l BURNING RATE MODlFlER The United States of America as represented by the Secretary of the Navy, Washington, DC.
Filed: Sept. 15, 1965 Appl. No.: 491,496
Assignee:
US. Cl. 149/193; 149/20; 149/44;
' 149/40 Int. Cl C06d 5/06 Field of Search 149/19, 19.3, 20, 44, 40
References Cited UNITED STATES PATENTS 11/1964 Horton 149/19.6
[ Apr. 8, 1975 Burke et a1. 149/193 X Stang 149/193 Burnside 149/193 Merrow et a1. 149/193 Kaufman 149/193 Julian et a1. 149/193 Primary E.\-aminerBenjamin R. Padgett Assistant E.\'aminerE. A. Miller Attorney, Agent, or Firm-R. S. Sciascia; Roy Miller ABSTRACT Solid fluorocarbon propellant compositions containing burning rate modifiers which have high structural integrity and a long storage life under varying environmental conditions.
6 Claims, N0 Drawings FLUOROCARBON SOLID PROPELLANT WITH BURNING RATE MODIFIER The invention described herein may be manufactured and used by or for the Government of the USA. for governmental purposes without the payment of any 'royalties thereon or therefor.
The present invention relates to improved solid propellants. A specific aspect relates to solid fluorocarbon propellants containing burning rate modifiers.
The fluorocarbon family of polymers has developed as excellent binders for composite solid propellants. Because of their high density, thermal stability, water impermeability, compatibility with a wide range of propellant ingredients, and high heat of reaction with metals, the fluorinated binders possess many desirable properties for propellant compositions. The propellants prepared with these binders have high structural integrity, long storage life, and good physical properties. The present invention provides a composition with increased burning rates, low pressure exponent or low temperature coefficient.
It is therefore an object of the present invention to provide a propellant with an improved burning rate for use in rocket motors and similar vehicles.
Another object is to provide a propellant with exceptionally high structural integrity and a long storage life under varying environmental conditions.
Yet another object is to provide an improved propeI- lant composition which can be produced in large volumes at low cost.
Other objects and many attendant advantages of this invention will be readily appreciated as the same be come better understood from the following description:
According to the present invention there is provided a propellant comprising up to 60 percent by weight of an oxidizer from 5 to 65 percent by weight of a binder consisting of a mixture of fluorocarbon polymers; up to 30 percent by weight metal fuel; and from 1 to 3 percent by weight chemical modifiers.
The oxidants which are applicable to the solid propellant of this invention are those oxygen-containing solids which readily give up oxygen and include ammonium, alkali metal and alkaline earth metal salts of nitric, perchloric, and chloric acids, and mixtures thereof. Ammonium perchlorate, potassium perchlorate, ammonium nitrate and hydrazine diperchlorate are preferred oxidizers for this invention.
The fluorocarbon polymers used in the composition consist of polytetrafluoroethylene (hereinafter referred to as Teflon) and a copolymer of vinylidene fluoride and hexafluoropropylene (hereinafter referred to as Viton-A) and mixtures thereof.
The high energy fuels preferred are aluminum, mag nesium, zirconium, uranium, thorium. beryllium and mixtures thereof. These metals will usually have a particle size within the ranges of l to 100 microns.
The chemical modifiers preferred for the present composition consist of copper, lead, tin, sodium, ammonium and potassium fluoborates; sodium, potassium, lithium, lead, copper, and calcium fluorides; potassium and ammonium dichromate; lead and zinc stearate; cesium carbonate; potassium and ammonium sulfate; copper chromite; oxides of magnesium, copper and manganese; boron; zinc dust; and carbon black.
One convenient method, and the presently preferred method, of preparing this composition comprises, first. dissolving the Viton-A in a solvent selected from a lowboiling ketone; acetone was used. The Teflon and other ingredients (fuel, oxidizer and modifier) were then thoroughly mixed into the Viton-A solution to form a uniform slurry or suspension. The slurry was washed for from 5 to 10 minutes with hexane, the volume of hexane being from 1 to 4 times the volume of slurry. By this step the Viton precipitates onto the other solids in the slurry. After the suspension had settled, the supernatant hexane was decanted and the resulting residue was dried under ambient conditions for from 8 to 24 hours. The slurry may be washed with normal hexane 2 or 3 times, as necessary.
A general formulation for a propellant composition prepared in accordance with the invention is as follows:
Ingredients Percent by weight Binder 5 to Viton-A 10 to 15 Teflon 5 to 50 Oxidizer up to 65 Metal Fuel up to 35 Chemical modifier l to 3 The following examples will serve to further illustrate the invention.
The above ingredients were processed by the shockgel technique described hereinbefore. The Viton is available in acetone solution for which an assay should be available. The solution should contain a minimum of 8 and a maximum of 22 weight percent Viton. All of the ingredients are added to a slurry pot. A volume of hexane equal to 4 times the volume of the Viton solution is placed in a container. While stirring the slurry, hexane is added slowly and mixing continues for about 15 minutes. The Viton is precipitated or shock-gelled onto the solids in the slurry. The supernatant hexane is siphoned off and an additional volume of fresh hexane, equal to the first volume, is added. Again, the supernatant hexane is siphoned off and the resulting composition is collected in a cloth bag and dried in a drying oven for from 8 to 24 hours at approximately F. Some of the material was extruded into strands for burning tests. This composition showed a burning rate at 1000 psi of 0.298-inch per second and a pressure exponent of 0.61.
The Viton-A is dissolved in acetone. To this solution the Teflon, aluminum, potassium perchlorate and sodium fluoride were added and mixed for about 10 minutes forming a slurry. The slurry was washed with hexane (4 volumes of hexane to 1 volume of Viton solution) for 10 minutes. The resulting mixture was let settle and hexane was siphoned off. The residue was washed with an additional volume of hexane for about 5 minutes. The supernatant hexane was again siphoned off, the composition collected in a cloth bag and dried. This material extrudes well. It showed a burning rate at 2000 psia of 0.63 inch per second and a pressure exponent of 0.53.
EXAMPLE Ill The following three samples (a, b and 0) using 300 grams each of the product prepared in Example II were modified with boron and copper chromite:
(a) Ingredients Weight in grams Composition of Example 11 300 Boron 6 About 300 grams of the cured composition prepared in Example [I were placed in a small sigma-blade mixer. The boron was suspended in about 100 ml of hexane, then poured into the mixer and thoroughly stirred for about 10 minutes. The product was transferred to a stainless steel container and dried overnight. Strands were extruded for burn rate determination.
(h) Ingredients Weight in grams Composition of Example 11 300 Copper chromite 6 The above ingredients were processed in the same manner as described in (a) above.
(c) Ingredients Weight in grams Composition of Example 11 300 Boron 3 Copper chromite 3 The boron and copper chromite were stirred into hexane, and the process proceeded as described hereinabove. Burn strands were extruded for burning rate determination.
Burning rate results for these three compositions are as follows:
(a) .98 in/sec; pressure exponent .68
The Viton was dissolved in acetone and all the ingredients were stirred therein for about 10 minutes forming a slurry orsuspension. The suspension was dropped into rapidly agitated hexane and stirred for 10 minutes. (About 4 volumes of hexane to one of Viton solution). After letting the composition settle out, the hexane was siphoned off. The composition was washed again with hexane which was decanted and the material was collected and dried. Some of this composition was extruded for burn rate determination.
EXAMPLE V Ingredients Percent by weight Function Viton-A l5 Binder Teflon l5 Binder Potassium perchlorate 49 Oxidizer Aluminum 18 Fuel Zinc(dust) 2 Modifier Sodium fluoride 1 Modifier These ingredients were processed as those in the previous examples. Burn strands formed from this composition showed a burning rate at 2000 psi of 0.74 inch per second and a pressure exponent of 0.77.
EXAMPLE VI Ingredients Percent by weight Function Viton-A l5 Binder Teflon l5 Binder Potassium perchlorate 49 Oxidizer Aluminum 18 Fuel Cupric oxide 2 Modifier Sodium fluoride I Modifier Strands of this composition gave a burning rate at 2000 psi of 0.68 inch per second and a pressure exponent of 0.82.
EXAMPLE VII Ingredients Percent by weight Function Viton-A l5 Binder Teflon l5 Binder Ammonium perchlorate 49 Oxidizer Aluminum 18 Fuel Lead 2 Modifier Sodium fluoride l Modifier Strands were extruded of this composition whiclgave a burning rate at 2000 psi of 0.76 inch per seconc and a pressure exponent of 0.78.
EXAMPLE Vlll Ingredients Percent by weight Function Teflon 51 Binder Viton-A 15 Binder Magnesium 31 Fuel Cuprie fluoride 3 Modifier The ingredients were processed in accordance witl the prior samples and strands were extruded for burn ing rate determination.
Polytetrafluoroethylene EXAMPLE X Ingredients Weight in grams Composition of Example ll 300 Copper fluorohorate 8 Since the fluoroborate used herein is hygroscopic, it is mixed into the basic formulation immediately prior to extrusion. Strands were extruded and burned with double dipped Viton inhibitor.
The above examples clearly demonstrate the effectiveness of the chemical modifiers on the fluorocarbon propellants which have great potential in the missile field today.
As will be evident to those skilled in the art various other modifications of the invention can be made, or-
followed. in view of the above disclosure, without departing from the spirit or scope of the invention.
What is claimed is: l. A solid propellant composition consisting essentially of the following:
Ingredients Percent by weight Copolymer of vinylidene fluoride and hexafluoropropylene Aluminum Potassium perchlorate Sodium fluoride Potassium dichromate 2. A solid propellant composition consisting essentially of the following:
Ingredients Percent by weight Polytetrafluoroethylene l 5 Copolymer of vinylidene fluoride and hexafluoropropylene 15 Aluminum Potassium perchlorate 43 Sodium fluoride 2.
3. A solid propellant composition consisting essentially of .the following:
Ingredients Percent by weight Polytetrafluoroethylene 16.3 Copolymer of vinylidene fluoride and hexafl uoropropylene l6.3 Potassium perch orate 65.2 Sodium fluoride 2.2.
4. A solid propellant composition consisting essentially of the following:
Ingredients Percent by weight Polytetrafluoroethylene Copolymer of vinylidene fluoride and hexafluoropro ylene Potassium perch orate 49 Aluminum l8 Zinc dust 2 Sodium fluoride l.
5. A solid propellant composition consisting essentially of the following:
ingredients Percent by weight Polytetrafluoroethylene 5 l Copolymer of vinylidene fluoride and hexafluoropropylene l5 Magnesium 3l Cupric fluoride 3.
6. A solid propellant composition consisting essentially of the following:
ingredients Percent by weight Polytetrafluoroethylene 4.9 Copolymer of vinylidene fluoride and hexafluoropropylene 14.7 Zirconium 36.9 Ammonium perchlorate 4l.5 Magnesium oxide 2.0.
Claims (6)
1. A SOLID PROPELLANT COMPOSITION CONSISTING ESSENTIALLY OF THE FOLLOWING: INGREDIENTS PERCENT BY WEIGHT
2. A solid propellant composition consisting essentially of the following:
3. A solid propellant composition consisting essentially of the following:
4. A solid propellant composition consisting essentially of the following:
5. A solid propellant composition consisting essentially of the following:
6. A solid propellant composition consisting essentially of the following:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US491496A US3876477A (en) | 1965-09-15 | 1965-09-15 | Fluorocarbon solid propellant with burning rate modifier |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US491496A US3876477A (en) | 1965-09-15 | 1965-09-15 | Fluorocarbon solid propellant with burning rate modifier |
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| Publication Number | Publication Date |
|---|---|
| US3876477A true US3876477A (en) | 1975-04-08 |
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| Application Number | Title | Priority Date | Filing Date |
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| US491496A Expired - Lifetime US3876477A (en) | 1965-09-15 | 1965-09-15 | Fluorocarbon solid propellant with burning rate modifier |
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| Country | Link |
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| US (1) | US3876477A (en) |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4000024A (en) * | 1975-10-17 | 1976-12-28 | The United States Of America As Represented By The Secretary Of The Air Force | Burning rate modifiers for solid propellants |
| US4001136A (en) * | 1974-12-30 | 1977-01-04 | The United States Of America As Represented By The Secretary Of The Air Force | Fluorine generating formulation for use in chemical lasers |
| US4001135A (en) * | 1974-12-30 | 1977-01-04 | The United States Of America As Represented By The Secretary Of The Air Force | Fluorine generating solid formulation for use in chemical lasers |
| US4152988A (en) * | 1977-09-19 | 1979-05-08 | The United States Of America As Represented By The Secretary Of The Navy | Electric match with epoxy coated fluorocarbon containing pyrotechnic composition |
| US4276100A (en) * | 1976-02-13 | 1981-06-30 | The United States Of America As Represented By The Secretary Of The Navy | Process for disposing of decoy flare material |
| US4971640A (en) * | 1989-08-04 | 1990-11-20 | Thiokol Corporation | Composite propellants containing copper compounds as ballistic modifiers |
| US5372664A (en) * | 1992-02-10 | 1994-12-13 | Thiokol Corporation | Castable double base propellant containing ultra fine carbon fiber as a ballistic modifier |
| US5470408A (en) * | 1993-10-22 | 1995-11-28 | Thiokol Corporation | Use of carbon fibrils to enhance burn rate of pyrotechnics and gas generants |
| US6132536A (en) * | 1997-08-20 | 2000-10-17 | The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration | Automated propellant blending |
| US6136111A (en) * | 1996-05-30 | 2000-10-24 | Quantic Industries, Inc. | Combustible composition for use in vehicle safety systems |
| US20040226638A1 (en) * | 2003-05-16 | 2004-11-18 | Posson Philip L. | Energetics binder of fluoroelastomer or other latex |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3156594A (en) * | 1964-06-10 | 1964-11-10 | Horton Marvin Duane | Polymeric base propellant compositions containing lithium fluoride catalyst |
| US3203171A (en) * | 1958-12-18 | 1965-08-31 | Burke | New missile fuel compositions containing halogens and method of propulsion |
| US3235422A (en) * | 1963-03-22 | 1966-02-15 | United Aircraft Corp | Fluorocarbon propellant |
| US3513043A (en) * | 1958-11-04 | 1970-05-19 | Phillips Petroleum Co | Composite solid propellants containing a perfluoroethylene resin,metal and a fluoroelastomer |
| US3732132A (en) * | 1964-11-23 | 1973-05-08 | Us Navy | Extrudable fluorocarbon propellants |
| US3734788A (en) * | 1964-04-17 | 1973-05-22 | Us Navy | High density solid propellants and method of preparation using fluoro-polymers |
| US3753811A (en) * | 1957-06-13 | 1973-08-21 | E Julian | Igniter composition |
-
1965
- 1965-09-15 US US491496A patent/US3876477A/en not_active Expired - Lifetime
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3753811A (en) * | 1957-06-13 | 1973-08-21 | E Julian | Igniter composition |
| US3513043A (en) * | 1958-11-04 | 1970-05-19 | Phillips Petroleum Co | Composite solid propellants containing a perfluoroethylene resin,metal and a fluoroelastomer |
| US3203171A (en) * | 1958-12-18 | 1965-08-31 | Burke | New missile fuel compositions containing halogens and method of propulsion |
| US3235422A (en) * | 1963-03-22 | 1966-02-15 | United Aircraft Corp | Fluorocarbon propellant |
| US3734788A (en) * | 1964-04-17 | 1973-05-22 | Us Navy | High density solid propellants and method of preparation using fluoro-polymers |
| US3156594A (en) * | 1964-06-10 | 1964-11-10 | Horton Marvin Duane | Polymeric base propellant compositions containing lithium fluoride catalyst |
| US3732132A (en) * | 1964-11-23 | 1973-05-08 | Us Navy | Extrudable fluorocarbon propellants |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4001136A (en) * | 1974-12-30 | 1977-01-04 | The United States Of America As Represented By The Secretary Of The Air Force | Fluorine generating formulation for use in chemical lasers |
| US4001135A (en) * | 1974-12-30 | 1977-01-04 | The United States Of America As Represented By The Secretary Of The Air Force | Fluorine generating solid formulation for use in chemical lasers |
| US4000024A (en) * | 1975-10-17 | 1976-12-28 | The United States Of America As Represented By The Secretary Of The Air Force | Burning rate modifiers for solid propellants |
| US4276100A (en) * | 1976-02-13 | 1981-06-30 | The United States Of America As Represented By The Secretary Of The Navy | Process for disposing of decoy flare material |
| US4152988A (en) * | 1977-09-19 | 1979-05-08 | The United States Of America As Represented By The Secretary Of The Navy | Electric match with epoxy coated fluorocarbon containing pyrotechnic composition |
| US4971640A (en) * | 1989-08-04 | 1990-11-20 | Thiokol Corporation | Composite propellants containing copper compounds as ballistic modifiers |
| US5372664A (en) * | 1992-02-10 | 1994-12-13 | Thiokol Corporation | Castable double base propellant containing ultra fine carbon fiber as a ballistic modifier |
| US5470408A (en) * | 1993-10-22 | 1995-11-28 | Thiokol Corporation | Use of carbon fibrils to enhance burn rate of pyrotechnics and gas generants |
| US6136111A (en) * | 1996-05-30 | 2000-10-24 | Quantic Industries, Inc. | Combustible composition for use in vehicle safety systems |
| US6132536A (en) * | 1997-08-20 | 2000-10-17 | The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration | Automated propellant blending |
| 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 |
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