USH717H - High burn rate ammonium perchlorate propellant - Google Patents
High burn rate ammonium perchlorate propellant Download PDFInfo
- Publication number
- USH717H USH717H US07/243,539 US24353988A USH717H US H717 H USH717 H US H717H US 24353988 A US24353988 A US 24353988A US H717 H USH717 H US H717H
- Authority
- US
- United States
- Prior art keywords
- weight percent
- tbd
- amount
- solid propellant
- catocene
- 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.)
- Abandoned
Links
Classifications
-
- 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
- Hycat 6D bis(ethyldicyclopentadienyliron)methane, registered under Trademark Hycat 6D.
- Hycat 6D migrated readily within the solid propellant producing unsatisfactory propellant properties.
- Hycat 6D has a total of six alpha hydrogens (hydrogen adjacent to aromatic ring). It is known that hydrogens adjacent to aromatic ring systems are susceptible to oxidation to form acids and/or hydroperoxides. Hydroperoxides are known to be highly unstable compounds.
- Catocene Since the alpha hydrogens were believed to be the reason for long term oxidation problems, Catocene was developed by coupling two ethylferrocenes with acetone, thus replacing the two bridged hydrogens with two methyl groups. Catocene then became the choice as a burn rate accelerator for ammonium perchlorate-based propellants. By replacing the two bridged hydrogens with methyl groups, long term oxidation and migration problems were reduced. However, accidental ignitions of solid propellants containing Catocene have occurred in both freshly prepared and aged propellants.
- an object of this invention is to provide a solid propellant composition which employs a dicyclopentadienyliron compound as a burn rate enhancer while retaining improved safety characteristics for the propellant formulation as compared with Catocene employed in a similar propellant formulation.
- the solid propellant formulation of this invention employing 2,2-bis(t-butyldicylopentadienyliron)propane (TBD) as the burn rate enhancer yields higher threshold values for ignition by impact and improved friction and spark testing values to thereby render the solid propellant formulation less hazardous to personnel during handling.
- TBD solid propellant formulations also give improved results of the desired pressure exponent, potlife, and maximum stress characteristics when compared to similar solid propellant formulation containing Catocene.
- the improved solid propellant composition having the properties described above is comprised of TBD as a burn rate enhancer in amounts from about 2 to about 6 weight percent, of about 68 weight percent of ammonium perchlorate of a trimodel blend of 200, 1.7, and 0.7 micron particle size, of aluminum powder of about 18 weight percent of a burner of hydroxyterminated polybutadience of about 9 weight percent, of an isocyanate curing agent as an additive of about 1 weight percent, and solid propellant processing aids in trace amounts.
- the solid propellant composition set forth below under Example illustrates the use of TBD as a burning rate enhancer with the formulation ingredients in weight percent.
- This formulation in above Example is mixed, cast, and cured by techniques and methods that are commonly used in the industry and that are known by personnel skilled in the art of propellant formulations.
- this solid propellant formulation is applicable to any program where there is a need for high burn rates and improved safety characteristics.
- Hycat 6D was a good burn rate enhancer, but was susceptible to long term oxidation. Hycat 6D also yielded poor results with respect to migration properties. Hycat 6D has a total of six alpha hydrogens (hydrogen adjacent to aromatic ring). It is believed that hydrogens adjacent to aromatic ring systems are suscepticle to oxidation to form acids and/or hydroperoxides. Hydroperoxides are known to be highly unstable compounds.
- Catocene was the next compound developed which showed early promise of meeting the burn rate enhancer requirement; however, it too had problems related to stability in spite of replacing two bridged hydrogens with two methyl groups as discussed below.
- Catocene Since the alpha hydrogens were believed to be the reason for long term oxidation problems, Catocene was developed by coupling two ethyferrocenes with acetone, thus replacing the two bridged hydrogens with two methyl groups. Catocene became a choice as a burn rate accelerator for ammonium perchlorate-based propellants. By replacing the two bridged hydrogens with methyl groups, long term oxidation and migration problems were reduced. However, accidental ignitions of propellants containing Catocene have occurred in both freshly prepared and aged propellants. Hence, the need for TBD was established.
- TBD The purpose of the work relating to TBD is to synthesize a compound that has no alpha hydrogens. TBD does not have hydrogens on carbon adjacent to the aromatic ring structure; therefore, long term oxidation and reduced problem of migration are among the benefits derived. TBD was synthesized and a propellant mix was evaluated and compared to a similar mix containing Catocene. ##STR1##
Abstract
A solid propellant composition employing 2,2-bis(t-butyldicyclopentadienyon)propane (TBD) as the burn rate enhancer in a weight percent from about 2 to about 6 weight percent yields higher threshold values for ignition by impact and improved friction and spark testing values to thereby render the solid propellant composition less hazardous to personnel during handling as compared to similar solid propellant compositions containing Catocene, (2,2-bis(ethyldicylopentadienyliron)propane). The TBD solid propellant composition also comprises from about 9 to about 10 weight percent of hydroxyterminated polybutadiene binder system including an isocyanate curative added in amount of up to 1.0 weight percent and optional modifiers in small amounts with adjustment of the weight percent of other ingredients. Other propellant ingredients comprise a trimodal mix of 200, 1.7, and 0.7 micron particle sizes of ammonium perchlorate oxidizer in amounts from about 66 to about 70 weight percent, and aluminum metal powder in amounts from about 18 to about 20 weight percent. TBD is synthesized to contain no alpha hydrogens, i.e., does not have hydrogens on carbon adjacent to the aromatic ring structure which contributes to long term oxidation and migration problems of Hycat 6D and Catocene.
Description
The invention described herein may be manufactured, used, and licensed by or for the Government for governmental purposes without the payment to us of any royalties thereon.
In line with the Army's continuing efforts to minimize hazards associated with propellant formulations used in its missile systems, a replacement propellant formulation has been sought that reduces some of the hazards associated with ammonium perchlorate propellants that use certain modifiers or additives such as 2,2-bis(ethyldicyclopentadienyliron)propane (also known as the trademark material Catocene) to enhance or increase propellant burn rate. Iron-containing compounds are now the current choice as burn rate enhancers for ammonium perchlorate propellants. Of these iron-containing compounds, ferrocene and its derivatives are the most efficient.
Earlier work with propellants containing solid iron compounds gave inconsistent burn rate enhancement because of the difficulty of getting a homogeneous mixture. Thereafter, liquid iron compounds were sought since it was believed that liquids would be better for mixing purposes. This plan of action lead to the development of bis(ethyldicyclopentadienyliron)methane, registered under Trademark Hycat 6D. Hycat 6D migrated readily within the solid propellant producing unsatisfactory propellant properties. Hycat 6D has a total of six alpha hydrogens (hydrogen adjacent to aromatic ring). It is known that hydrogens adjacent to aromatic ring systems are susceptible to oxidation to form acids and/or hydroperoxides. Hydroperoxides are known to be highly unstable compounds.
Since the alpha hydrogens were believed to be the reason for long term oxidation problems, Catocene was developed by coupling two ethylferrocenes with acetone, thus replacing the two bridged hydrogens with two methyl groups. Catocene then became the choice as a burn rate accelerator for ammonium perchlorate-based propellants. By replacing the two bridged hydrogens with methyl groups, long term oxidation and migration problems were reduced. However, accidental ignitions of solid propellants containing Catocene have occurred in both freshly prepared and aged propellants.
Therefore, the current status of Catocene in light of the concern for safety, where accidental ignition has been a problem for both freshly prepared and aged propellants, has motivated the development of a dicyclopentadienyliron compound that performs at the level of Catocene while having improved safety characteristics.
Therefore, an object of this invention is to provide a solid propellant composition which employs a dicyclopentadienyliron compound as a burn rate enhancer while retaining improved safety characteristics for the propellant formulation as compared with Catocene employed in a similar propellant formulation.
The solid propellant formulation of this invention employing 2,2-bis(t-butyldicylopentadienyliron)propane (TBD) as the burn rate enhancer yields higher threshold values for ignition by impact and improved friction and spark testing values to thereby render the solid propellant formulation less hazardous to personnel during handling. TBD solid propellant formulations also give improved results of the desired pressure exponent, potlife, and maximum stress characteristics when compared to similar solid propellant formulation containing Catocene.
The improved solid propellant composition having the properties described above is comprised of TBD as a burn rate enhancer in amounts from about 2 to about 6 weight percent, of about 68 weight percent of ammonium perchlorate of a trimodel blend of 200, 1.7, and 0.7 micron particle size, of aluminum powder of about 18 weight percent of a burner of hydroxyterminated polybutadience of about 9 weight percent, of an isocyanate curing agent as an additive of about 1 weight percent, and solid propellant processing aids in trace amounts.
The solid propellant composition set forth below under Example illustrates the use of TBD as a burning rate enhancer with the formulation ingredients in weight percent.
______________________________________ WEIGHT WEIGHT PERCENT INGREDIENT PERCENT RANGE ______________________________________ Binder.sup.1,4 9.0 9-10 TBD.sup.2 5.0 2-6 Aluminum powder 18.0 18-20 Ammonium Perchlorate.sup.3 68.0 66-70 ______________________________________ Notes: .sup.1 Hydroxyterminated Polybutadiene (HTPB) binder system including an isocyanate curative as an additive up to about 1 weight percent. .sup.2 TBD concentration can be varied from 2-6% to give the desired burn rate. .sup.3 The ammonium perchlorate is a trimodal mix of particle sizes 200, 1.7, and 0.7 microns. .sup.4 Other additives, isocyanate curatives and modifiers can be added i small quantities with adjustment of the percent of content of other ingredients as required for desired performance.
This formulation in above Example is mixed, cast, and cured by techniques and methods that are commonly used in the industry and that are known by personnel skilled in the art of propellant formulations.
The use of this solid propellant formulation is applicable to any program where there is a need for high burn rates and improved safety characteristics.
The structural formulae (A and B) of Hycat 6D, and Catocene, respectively, are presented below for comparison with TBD; the structural formula (C) for TBD is also presented below. Hycat 6D was a good burn rate enhancer, but was susceptible to long term oxidation. Hycat 6D also yielded poor results with respect to migration properties. Hycat 6D has a total of six alpha hydrogens (hydrogen adjacent to aromatic ring). It is believed that hydrogens adjacent to aromatic ring systems are suscepticle to oxidation to form acids and/or hydroperoxides. Hydroperoxides are known to be highly unstable compounds.
Catocene was the next compound developed which showed early promise of meeting the burn rate enhancer requirement; however, it too had problems related to stability in spite of replacing two bridged hydrogens with two methyl groups as discussed below.
Since the alpha hydrogens were believed to be the reason for long term oxidation problems, Catocene was developed by coupling two ethyferrocenes with acetone, thus replacing the two bridged hydrogens with two methyl groups. Catocene became a choice as a burn rate accelerator for ammonium perchlorate-based propellants. By replacing the two bridged hydrogens with methyl groups, long term oxidation and migration problems were reduced. However, accidental ignitions of propellants containing Catocene have occurred in both freshly prepared and aged propellants. Hence, the need for TBD was established.
The purpose of the work relating to TBD is to synthesize a compound that has no alpha hydrogens. TBD does not have hydrogens on carbon adjacent to the aromatic ring structure; therefore, long term oxidation and reduced problem of migration are among the benefits derived. TBD was synthesized and a propellant mix was evaluated and compared to a similar mix containing Catocene. ##STR1##
During the development program for TBD in solid propellants, several areas of interest were evaluated to determine the properties of a solid propellant composition containing TBD as compared to one containing Catocene.
The areas of interest evaluated are summarized in Table I. Sensitivity Results; Table II. One-Gallon Mix Data; and Table III. Pint Mix Preliminary Ballistic Data as follows:
TABLE I ______________________________________ SENSITIVITY RESULTS Cured Sensitivity Impact Spark Friction Mix No. Percent Catalyst (lb-cm) (joules) (lb) ______________________________________ 27 (TBD) 6 78 0.125 60 29 (TBD) 5 66 2.25 60 30 (TBD) 5 60 1.00 50 31 (TBD) 5 72 4.00 90 32 (TBD) 0 74 25 90 49 (TBD) 6 78 1.00 ND 1-gallon (TBD) 5 74 6.25 80 Catocene Mix 5 48 1.00 50 ______________________________________
TABLE II ______________________________________ ONE-GALLON MIX DATA Catalyst (%) TBD 5% Catocene 5% ______________________________________ EOM Viscosity, KP 3 4 Potlife to 40 Kp, Hr 16.4 14 NCO/OH 0.89 0.89 Maximum Stress, psi 423 251 Strain at Max. Stress, 28 35 percent Tangent Modulus 1893 812 Burn Rate @ 1000 psi 3.12 3.19 @ 2000 psi 4.20 4.33 Pressure Exponent 0.43 0.46 ______________________________________
TABLE III ______________________________________ PINT MIX PRELIMINARY BALLISTIC DATA Burn Rate @ 1000 2000 Pressure Mix No. % TBD (psi) (psi) Exponent ______________________________________ 27 6 2.95 3.98 0.44 29 5 3.22 4.33 0.43 30 5 3.20 4.25 0.42 31 5 3.20 4.25 0.42 32 0 0.46 0.98 0.72 (1.00 @ 2000 psi) 49 6 3.50 4.78 0.45 ______________________________________
Claims (2)
1. A solid propellant composition comprising:
(i) a trimodal mix of particle sizes 200, 1.7, and 0.7 microns of ammonium perchlorate oxidizer in an amount from about 66 to about 70 weight percent, said trimodal mix having a major portion of said 1.7 and 0.7 micron particle sizes with the remainder of said weight percent being 200 micron particle size;
(ii) hydroxyterminated polybutadiene binder system in an amount from about 9 to about 10 weight percent, said hydroyx-terminated polybutadiene binder system including an isocyanate curative added in an amount of up to about 1.0 weight percent and optional modifiers in small amounts with adjustment of the weight of other ingredients;
(iii) aluminum metal powder from about 18 to 20 weight percent; and,
(iv) a burning rate enhancer of 2,2-bis(t-butyldicylopentadienyliron)propane in amount from about 2 to about 6 weight percent.
2. The solid propellant composition of claim 1 wherein said trimodial mix of said ammonium perchlorate is present in an amount of about 68 weight percent; said hydroxyterminated polybutadiene binder system is present in amount of about 9 weight percent; said aluminum metal powder is present in an amount of about 18 weight percent; and wherein said burn rate enhancer of 2,2-bis(t-butyldicyclopentadienyliron)propane is present in an amount of about 5 weight percent.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/243,539 USH717H (en) | 1988-09-12 | 1988-09-12 | High burn rate ammonium perchlorate propellant |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/243,539 USH717H (en) | 1988-09-12 | 1988-09-12 | High burn rate ammonium perchlorate propellant |
Publications (1)
Publication Number | Publication Date |
---|---|
USH717H true USH717H (en) | 1989-12-05 |
Family
ID=22919147
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US07/243,539 Abandoned USH717H (en) | 1988-09-12 | 1988-09-12 | High burn rate ammonium perchlorate propellant |
Country Status (1)
Country | Link |
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US (1) | USH717H (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5112417A (en) * | 1991-05-20 | 1992-05-12 | United States Of America | Method of controlling the increase in potlife of propellants during processing |
US5281286A (en) * | 1992-04-09 | 1994-01-25 | The United States Of America As Represented By The Secretary Of The Army | Microcoacervation of propellant ingredients |
US5872328A (en) * | 1996-03-06 | 1999-02-16 | Chemische Betriebe Pluto Gmbh | Ferrocene derivatives |
US6217682B1 (en) | 1997-10-27 | 2001-04-17 | Cordant Technologies Inc. | Energetic oxetane propellants |
US6740180B1 (en) * | 1997-07-15 | 2004-05-25 | Anthony Joseph Cesaroni | Thermoplastic polymer propellant compositions |
US6815522B1 (en) | 1998-11-12 | 2004-11-09 | Alliant Techsystems Inc. | Synthesis of energetic thermoplastic elastomers containing oligomeric urethane linkages |
US6997997B1 (en) | 1998-11-12 | 2006-02-14 | Alliant Techsystems Inc. | Method for the synthesis of energetic thermoplastic elastomers in non-halogenated solvents |
US7011722B2 (en) | 2003-03-10 | 2006-03-14 | Alliant Techsystems Inc. | Propellant formulation |
US20060157173A1 (en) * | 1998-11-12 | 2006-07-20 | Sanderson Andrew J | Synthesis of energetic thermoplastic elastomers containing both polyoxirane and polyoxetane blocks |
US7101955B1 (en) | 1998-11-12 | 2006-09-05 | Alliant Techsystems Inc. | Synthesis of energetic thermoplastic elastomers containing both polyoxirane and polyoxetane blocks |
-
1988
- 1988-09-12 US US07/243,539 patent/USH717H/en not_active Abandoned
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5112417A (en) * | 1991-05-20 | 1992-05-12 | United States Of America | Method of controlling the increase in potlife of propellants during processing |
US5281286A (en) * | 1992-04-09 | 1994-01-25 | The United States Of America As Represented By The Secretary Of The Army | Microcoacervation of propellant ingredients |
US5872328A (en) * | 1996-03-06 | 1999-02-16 | Chemische Betriebe Pluto Gmbh | Ferrocene derivatives |
US6740180B1 (en) * | 1997-07-15 | 2004-05-25 | Anthony Joseph Cesaroni | Thermoplastic polymer propellant compositions |
US6217682B1 (en) | 1997-10-27 | 2001-04-17 | Cordant Technologies Inc. | Energetic oxetane propellants |
US6815522B1 (en) | 1998-11-12 | 2004-11-09 | Alliant Techsystems Inc. | Synthesis of energetic thermoplastic elastomers containing oligomeric urethane linkages |
US6997997B1 (en) | 1998-11-12 | 2006-02-14 | Alliant Techsystems Inc. | Method for the synthesis of energetic thermoplastic elastomers in non-halogenated solvents |
US20060074215A1 (en) * | 1998-11-12 | 2006-04-06 | Sanderson Andrew J | Synthesis of energetic thermoplastic elastomers containing oligomeric urethane linkages |
US20060157173A1 (en) * | 1998-11-12 | 2006-07-20 | Sanderson Andrew J | Synthesis of energetic thermoplastic elastomers containing both polyoxirane and polyoxetane blocks |
US7101955B1 (en) | 1998-11-12 | 2006-09-05 | Alliant Techsystems Inc. | Synthesis of energetic thermoplastic elastomers containing both polyoxirane and polyoxetane blocks |
US20090088506A1 (en) * | 1998-11-12 | 2009-04-02 | Alliant Techsystems Inc. | Synthesis of energetic thermoplastic elastomers containing both polyoxirane and polyoxetane blocks |
US7011722B2 (en) | 2003-03-10 | 2006-03-14 | Alliant Techsystems Inc. | Propellant formulation |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: UNITED STATES OF AMERICA, THE, AS REPRESENTED BY T Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNORS:STEPHENS, WILLIAM D.;WARREN, LARRY C.;REEL/FRAME:005149/0744;SIGNING DATES FROM 19880901 TO 19880906 |
|
STCF | Information on status: patent grant |
Free format text: PATENTED CASE |