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Publication numberUS3756874 A
Publication typeGrant
Publication dateSep 4, 1973
Filing dateJul 1, 1969
Priority dateJul 1, 1969
Publication numberUS 3756874 A, US 3756874A, US-A-3756874, US3756874 A, US3756874A
InventorsChang M, Lowe J
Original AssigneeUs Navy
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Temperature resistant propellants containing cyclotetramethylenetetranitramine
US 3756874 A
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Description  (OCR text may contain errors)

Sept. 4, 1973 M. s. CHANG ETAL 3,756,87

TEMPERATURE RESISTANT PROPELLANTS CONTAINING CYCLOTETRAMETHYLENETETRANITRAMINE Filed July 1, 1969 o I l l 1 l i I J 500 I000 2000 4000 Pressure (psi) STRAND BURNING RATE VERSUS PRESSURE 69% HMX, l5/ potassium perchlorate, l6 polyglycol adipate Burning rate (in/sec) or a 01 m an o I l I I l 0 l l l l 500 I000 2000 4000 Pressure (psi) STRAND BURNING RATE VERSUS PRESSURE 69% HMX, l5 potassium perchlorate, l4 poiygiycoi adipaie, 2 copper chromite 3,756,874 Patented Sept. 4, 1973 3,756,874 TEMPERATURE RESISTANT PROPELLANTS CON- TAINING CYCLOTETRAMETHYLENETETRANI- TRAMINE Marguerite S. Chang, Forest Heights, and James U. Lowe, Jr., Landover, Md., assignors to the United States of America as represented by the Secretary of the Navy Continuation-impart of application Ser. No. 643,292, May 23, 1967. This application July 1, 1969, Ser. No. 839,802

Int. Cl. C06d /06 US. Cl. 149-19 9 Claims ABSTRACT OF THE DISCLOSURE An oxidant for composite propellants comprising the admixture of HMX with potassium perchlorate.

A composite propellant wherein the above oxidant is incorporated with a fuel-matrix binder.

CROSS REFERENCE TO RELATED APPLICATION This is a continuation-in-part of application Ser. No. 643,292, filed May 23, 1967, now abandoned.

BACKGROUND OF INVENTION This invention relates generally to composite type propellants and more specifically to a new oxidant mixture for composite type propellants and a novel composite propellant using the aforementioned oxidant.

Solid propellants are classified as either double base or composite depending upon their composition. The composite type is characterized by high thermal stability and burning rate and generally consists of a finely ground crystalline oxidant dispersed in a matrix of a plastic, resinous or elastomeric fuel. The double base compositions are characterized by high impetus and high burning rate and generally consist of an unstable self-combustible material such as the mixture of nitrocellulose with nitroglycerin.

Recent developments in the field of cartridge activated devices, specifically in the field of emergency personnel escape devices, have now generated a demand for a propellant characterized not only by high impetus and high burning rate, normally characteristic of double base propellant, but also by high temperature thermal stability 300 F.) normally characteristic of the composite propellant. Neither the presently available composite nor the presently available double base propellants are capable of meeting these more stringent requirements; the double base type is insufficiently thermally stable and the composite type, while satisfying the high thermal stability, impetus and burning rate, tends to form corrosive and toxic gases and large quantities of carbon and carbon monoxide as by-products of combustion.

Since the oxidizer is the major constituent of composite propellants it contributes most to burning characteristics. The most common oxidizers presently available to the art have been potassium perchlorate, ammonium perchlorate, ammonium nitrate and sodium and potassium nitrate. While potassium or sodium perchlorate are characterized by relatively high burning rates and high flame temperatures, they tend to produce large quantities of corrosive and toxic hydrogen chloride gas which tends to destroy the cartridge and bomb ejector hardware. They also tend to produce a very dense smoke of the respective chloride salts and are subject to secondary flash characteristics. Sodium perchlorate is further unsuitable due to its high water solubility and high hydroscopicity.

Formulations containing ammonium perchlorate have a significantly lower burning rate and flame temperature and although not subject to formation of excessive smoke to tend to produce corrosive gases and are also nude sirably hygroscopic. The nitrates are excessively slow burning and possess unduly low flame temperatures.

SUMMARY OF INVENTION Accordingly it is an object of this invention to provide an improved composite propellant suitable for use in cartridge activated personnel escape devices.

Another object of this invention is to provide an oxidant for composite propellants, characterized by high impetus, high burning rate and high thermal stability (above about 300 F.) yet which is clean burning and does not form toxic and corrosive gases during combustion.

These and other objects are attained by providing a novel oxidant mixture in which a portion of the oxidant is a nitramine composition. Specifically these objects are attained by providing the mixed oxidant composition of from about 5-45 parts by weight of potassium perchlorate with from about -55 parts by weight of cyclotetramethylenetetranitramine (HMX). The oxidant mixture of this invention incorporates the thermal stability, nonhygroscopicity, high burning rate and. high impulse characteristics of potassium perchlorate with the low corrosion and clean burning properties of the nitramines.

DESCRIPTION OF THE DRAWINGS FIG. 1 and FIG. 2 are graphical representations of the burning rate performance characteristics of the preferred embodiments of this invention.

DETAILED DESCRIPTION The composite propellants of this invention may use any elastomeric, plastic or resinous binder as the fuel matrix, such as the polyurethanes, polysulfide rubber, polyvinylchloride, epoxy resins, polyesters, hydrocarbon rubber, asphalt or acrylic polymers. Among those binders which are particularly applicable are the polymers of butadiene and acrylic acid such as Butarez CTL-II, the polymerization product of ethylenediamine and linoleic acid, the terpolymer of 2-methyl-S-vinyl-tetrazole/ethyl acrylate/acrylic acid, which is the subject of Navy Case 45,473 submitted by H. S. Haiss and J. U. Lowe, Jr., polyglycol adipate, and epoxy resins such as Epon 812, the diglycidyl ether of bisphenol A. The binder may additionally be cured with any of the common crosslinking agents such as DER-332 a diepoxide (MAPO) trisrnethylaziridinyl phosphine oxide and chromium naphthanate, and the like.

Preferably the nitramine component is mixed with potassium perchlorate in a ratio of 19:1 to 12:1. More preferably however is the admixture of from 80-60 parts by weight nitramine with 10-30 parts by weight potassium perchlorate.

The oxidant mixture is generally present in amounts of from about 50-95 parts per parts of propellant, and more preferably in amounts of from almost 80-95 parts per 100 parts of propellant.

Other additives normally incorporated into solid oxidants and composite propellants may be added herein, such as any of the various accelerators, burning rate catalysts, extenders, reinforcing agents and fillers.

Burning characteristics may be improved for example by incorporating ammonium picrate, ferrocene, or aluminum powder, or the grains may be glazed with carbon black as a reinforcing agent. Burning rates can easily be obtained between 0200-0400 in./sec. at 1000 psi.

The burning rate exponent (n) of Vieilles law, may be improved by incorporating a synergist such as those described in US. Pat. 3,138,499 filed by A. T. Camp which include copper chromite, lead salicylate, lead stearate and lead resorcylate. A preferred burning rate modifier is lead chromate (PbCrO To more clearly illustrate the present invention reference is made to the following examples which are presented for purposes of illustration and not to be restrictive in any manner. The following formulations were-prepared in 2 pound quantities.

Example I exhaust,

Time (hr.): Weight loss (percent Impetus: 369,800lbf./1b. Pressure exponent (n): 0.87

Example II Composition: 69% HMX, 15 potassium perchlorate,

14% polyglycol adipate, 2% copper chromite Density: 1.735 g./cc. Specific impulse, ideal: 228.87 lbf.-sec./lbm. Flame temperature: Chamber 4173 F.: exhaust 155 8 F. Impact sensitivity: 3 til, 200 mm. (5-kg. Wt.): 20 til, 328

mm. (2-kg. wt.) Vacuum stability: 0.45 cc./g., 248 F./40 hr. Autoignition temperature (DTA): 441 F. Weight loss after storage of 28 days at 203 F.: 0.4% 1) Burning rate: 0.248 in./sec. at 1000 p.s.i. (2) Burning rate after storage: 0.237 in./sec. at 1000 p.s.i. Weight loss after storage of 4 hours at 400 F.: 5.8% Thermal stability at 302 R:

Time (hr.): Weight loss (percent) 24 0.86

Burning rate after 445 hr. at 302 F.: 0.297 in./sec. at

1000 p.s.i.

Impetus: 365,000 lbf./lb. Pressure exponent (n): 0.82

The variation of burning rate with temperature and pressure of these propellants is shown in FIGS. 1 and 2. n is the slope of the curve plotted on the log-log scale and represents the burning rate constant.

Burning rate at 1000 p.s.i. (in./sec.): 0.401

4 Example V Percent HMX 64 Potassium nitrate 20 Lead carbonate 2 PGA 14 Burning rate at 1000 p.s.i. (in./sec.): 0.227

Example VI Percent HMX 69 Potassium perchlorate 15 Butarez CTL-II 12 DER-332 0.5 MAPO 1.3 Chromium naphthenate 0.2 Copper chromite 2 Burning rate at 1000 p.s.i. (in./sec.): 0.235

Example VII Composition: 69% HMX, 15% potassium perchlorate,

14% polyglycol adipate, 2% PbCrO Density: 1.846 g./cc. Impact sensitivity: 3 til, mm. (5 kg. wt.) 20 til, Allegany Balistics Laboratory tools, 262 mm. (2 kg.

wt.) Vacuum stability: 0.35 and 0.27 cc./g. at 248 F./40 hr. Autoignition temperature (DTA): 452 F. (18 F./min.) Thermal stability at 302 F.: 500 hours with less than 10% weight loss Thermal stability at 400 F. for 4 hours: Weight loss 2.4% Burning rate exponent (n): 0.83 (750 to 3000 p.s.i.)

1rk=0.49% F. a 0.10% F. Mechanical properties: Sm 258 p.s.i., Em 6.15% Impetus: 4.3 x10 in. lb./lb.

In the foregoing examples impact sensitivity was determined. by subjecting a small quantity of confined explosive to the transmitted shock from a falling weight (5 kg. and 2 kg.), and by determining the minimum height of fall that will cause at least one explosion in a given number of drops. In the Allegany Ballistics Laboratory test, 0.02 gm. of the material to be tested is spread evenly over an area of 1 cm. in diameter and confined by means of a plunger having a tip 1 cm. in diameter. A falling weight of 2 kg. strikes the upper end of the plunger. The results are recorded as minimum height to effect explosion in 20 drops.

To check the accuracy of this test, impact sensitivity was measured using a standard 5 kg. weight and the minimum height to effect explosion in 3 drops was recorded.

Vacuum stability measurements were made by placing a 1 gm. sample into an evacuated chamber situated in a hot water bath of 248 F. for 40 hours. The amount of gas formed was recorded in cc./ gm.

Table I below contains comparative data illustrating the unexpected greater thermal stability of the HMX compositions of the present invention over similar RDX formulations.

Other advantages of the propellants of this invention will be apparent to those skilled in the art in view of the above disclosure and various modifications can be made without departing from the scope of this invention.

What is claimed as new and desired to be secured by Letters Patent of the United States is:

1. A solid oxidizer for a composite type propellant comprising the admixture of from about -45 parts by weight of potassium perchlorate with from about 95-55 parts by weight of cyclotetramethylenetetranitramine.

2. A composite type, thermally stable, low corrosive propellant which comprises:

(a) an oxidizer comprising the admixture of from about 5-45 parts by weight of potassium perchlorate with 95-55 parts by weight of cyclotetramethylenetetranitrarnine and (b) a matrix of a fuel-binder composition selected from the group consisting of polysulfide rubber, polyurethane, polyvinylchloride, epoxy resins, polyesters, hydrocarbon rubber, asphalt and acrylic polymer.

3. The composite type propellant of claim 2 wherein the fuel-binder composition is selected from the group consisting of poly (butadiene-acrylic acid), the polymerization product of ethylenediamine and linoleic acid, the terpolymer of Z-methyl-5-vinyl-tetrazole, ethyl acrylate and acrylic acid, and the diglycidyl ether of bisphenol A.

4. The composite type propellant of claim 2 wherein the fuel-binder composition is the terpolymer of 2-methyl-5-vinyl-tetrazole, ethyl acrylate and acrylic acid.

5. The composite type propellant of claim 2 wherein the fuel-binder composition is polyglycol adipate.

6. The composite type propellant of claim 2 wherein the fuel-binder composition is the diglycidyl ether of bisphe-nol A.

7. The composite type propellant composition of claim 2 wherein a small quantity of a burning rate synergist is admixed with (a) 8. The composite type propellant composition of claim 7 wherein the burning rate synergist is selected from the group consisting of lead chromate, copper chromite, lead salicylate, lead stearate, and lead B-resorcylate.

9. The composite type propellant composition of claim 5 which comprises, on a weight percent basis, 69 percent of cyclotetramethylenetetranitramine, 15 percent potassium perchlorate, 14 percent polyglycol adipate and 2 percent lead chromate.

References Cited UNITED STATES PATENTS 2,995,430 8/1961 Scharf 149-19 3,002,830 10/1961 'Barr 149l9 3,046,829 7/1962 Roemer 149-19 X 3,068,129 12/1962 Schaffel 149l9 3,123,507 3/1964 Butt et a1. 14992 X 3,269,880 8/1966 Visnov 149-92 X BENJAMIN R. PADGETI, Primary Examiner US. Cl. XJR.

Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3839106 *Apr 9, 1971Oct 1, 1974Poudres & Explosifs Ste NaleComposite explosive with a carboxylic polydiolefin binder
US3896865 *Jan 21, 1974Jul 29, 1975Us NavyPropellant with polymer containing nitramine moieties as binder
US4042430 *Apr 10, 1972Aug 16, 1977The United States Of America As Represented By The Secretary Of The NavyTemperature resistant explosive containing diaminotrinitrobenzene
US4078495 *Aug 15, 1974Mar 14, 1978The United States Of America As Represented By The Secretary Of The NavyCyclonite in binder of ethylhexyl acrylate, vinylpyrrolidone, and dioctyl maleate
US4180424 *Jul 11, 1977Dec 25, 1979The United States Of America As Represented By The Secretary Of The ArmyControl of burning rate and burning rate exponent by particle size in gun propellants
US4239073 *Jan 17, 1973Dec 16, 1980Thiokol CorporationBinder synergistically reacts with the oxidizer
US4361450 *Jun 2, 1975Nov 30, 1982Thiokol CorporationPlastic bonded explosive compositions
US4385948 *Aug 7, 1980May 31, 1983The United States Of America As Represented By The Secretary Of The NavyIn situ cured booster explosive
US4406210 *Feb 17, 1981Sep 27, 1983Brunswick CorporationJet-propelled missile with single propellant-explosive
US4874441 *Dec 28, 1988Oct 17, 1989Advanced Explosives Gesellschaft B.R.Mixture of perchlorate, metal, desensitizer, and binder
US5449423 *Oct 13, 1992Sep 12, 1995Cioffe; AnthonyPropellant and explosive composition
US5591936 *Aug 2, 1990Jan 7, 1997Thiokol CorporationPolyglycidyl nitrate
US5633476 *Jun 7, 1995May 27, 1997Cioffe; AnthonyMixing nitrate oxidizer, potassium perchlorate, organic acid at low temperature, low humidity
US5798480 *Aug 2, 1990Aug 25, 1998Cordant Technologies Inc.High performance space motor solid propellants
US5801325 *Aug 2, 1990Sep 1, 1998Cordant Technologies Inc.High performance large launch vehicle solid propellants
US7344610Jan 28, 2003Mar 18, 2008Hodgdon Powder Company, Inc.Sulfur-free propellant compositions
EP0323828A1 *Jan 3, 1989Jul 12, 1989ADVANCED EXPLOSIVES GESELLSCHAFT b.RExplosive for war heads and solid propellants
Classifications
U.S. Classification149/19.4, 149/20, 149/19.5, 149/92, 149/19.9, 525/375, 149/19.91, 149/19.6
International ClassificationC06B25/34, C06B45/00, C06B45/10, C06B25/00
Cooperative ClassificationC06B25/34, C06B45/10
European ClassificationC06B25/34, C06B45/10