CA1039062A - Smokeless stable burning propellant - Google Patents

Smokeless stable burning propellant

Info

Publication number
CA1039062A
CA1039062A CA201,806A CA201806A CA1039062A CA 1039062 A CA1039062 A CA 1039062A CA 201806 A CA201806 A CA 201806A CA 1039062 A CA1039062 A CA 1039062A
Authority
CA
Canada
Prior art keywords
composition according
carbon
carbide
microns
burning
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.)
Expired
Application number
CA201,806A
Other languages
French (fr)
Inventor
Gilbert A. Zimmerman
Joseph Cohen
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Aerojet Rocketdyne Inc
Original Assignee
Aerojet General Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Aerojet General Corp filed Critical Aerojet General Corp
Application granted granted Critical
Publication of CA1039062A publication Critical patent/CA1039062A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B45/00Compositions or products which are defined by structure or arrangement of component of product
    • C06B45/02Compositions or products which are defined by structure or arrangement of component of product comprising particles of diverse size or shape
    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B23/00Compositions characterised by non-explosive or non-thermic constituents
    • C06B23/04Compositions characterised by non-explosive or non-thermic constituents for cooling the explosion gases including antifouling and flash suppressing agents
    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B33/00Compositions containing particulate metal, alloy, boron, silicon, selenium or tellurium with at least one oxygen supplying material which is either a metal oxide or a salt, organic or inorganic, capable of yielding a metal oxide
    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B45/00Compositions or products which are defined by structure or arrangement of component of product
    • C06B45/04Compositions 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
    • C06B45/06Compositions 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
    • C06B45/10Compositions 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
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S149/00Explosive and thermic compositions or charges
    • Y10S149/11Particle size of a component

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Dispersion Chemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Molecular Biology (AREA)
  • Solid Fuels And Fuel-Associated Substances (AREA)
  • Portable Nailing Machines And Staplers (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Air Bags (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

SMOKELESS STABLE BURNING PROPELLANT

Abstract of the Disclosure (C) Ammonium perchlorate propellants utilizing a polybutadiene binder provide a smokeless exhaust and burn stably in a motor at a burning rate above 0.40 in/sec at 1,000 psia with no combustion instability if they include 0.2-5% of refractory metal carbides or oxides and carbon in the form of hollow, broken or unbroken carbon spheres, carbon particles or carbon flakes.

Description

1039~Z
.
Background of the Invention (U) 1. Field of the Invention The present invention relates to stable burning, smokeless propellants and more particularly to high energy, ammonium perchlorate propellants based on a polybutadiene binder.
(U) 2. Description of the Prior Art ~ he absence of a visible exhaust from a solid rocket motor is a highly desirable attribute, particularly for military applications. Such performance is possible by eliminating from the propellant formulation any material which will form a solid -particulate on combustion (primary smoke). Double-base (nitrocellulose-nitroglycerin) compositions have been the principal propellants used for smokeless applications. Although more desirable becauæe of higher performance, the composite propellants based on ammoniu~ perchIorate in an organic binder have used ~-materials which ~orm solid particulates, principally aluminum, to ~
eliminate combustion instability and maximize specific impulse. -.~ ~
~ Eliminating aluminum from the composite system eliminates primary smoke ' but brin~s in the problem o~ combustion inætability when the propellants are formulated with high oxidizer content for high specific impulse.
(C) Recent work ha~ shown that smokeless ammonium perchlorate (AP) propellants using a hydroxy-terminated polybutadiene (HTPB) binder will yield a smokeless exhaust (primary smoke) and burn stably in a motor if the burning rate is about 0.40 in/s0c or lower at 1,000 psia. At burning rates above this level, combustion instability has limited the usefulness of such compositions.
(U) Smoke is defined in terms of solid-propellant exhaust as including all visible signature effects with the exception of flash or luminosity effects. Smoke is more strictly considered to be of two general categories: either primary, wherein solid particles in the propellant exhaust affect its light transmissivity -independently of the environment, or secondary (induced), wherein ;
some of the gaseous components in the exhaust such as HCl, HF, N02 ; or condensible w~ter vapor interact with the ambient air to produce visible aerosols of liquid or solid particles. Sources of primary smoke from the propellant include unburned carbon and , 20 metal oxides.
(U) The selection of any propellant involves the determination of performance factors, safety factors, life factors and cost ~ factors. Performance factors to be considered include spec ific s~ -.,, . :
; impulse, density and thermal expansion characteristics, me chanical ; properties, burning rate, combustion stability, sensitivit y of chamber pressure to grain temperature and propellant erosi vity.
Safety factors include sensitivity to impact, friction, dr opping, fire and spark. Also to be considered under safety are thermal stability or auto ignition temperature, processing hazards, toxicity and exhaust product toxicity. Life factors include polymer deg radation, ,, .

.

. - :. ~. ... . : , : . . . -1039(~6Z ~ ~
moisture sensitivity, plasticizer migration and catastrophic phenomena connected with grain cracking and bond failure.
Previously, smokelessness resulted in definite penalties in one --;
or more of these factors or determinates of the factors.
Combu6tion instability is a complex phenomena involving the combination of the inner motor configuration and dimensions as well as propellant. A motor exhibits instabilitg when the burning response of the propellant to pressure and velocity fluctuations interacts with the acoustics of the chamber cavity such that, at one or more frequencies, the acoustic energy added ; to the system by the propellant exceeds that which is dissipated by --frictional damping or carried from the chamber convectively.
Because the phenomena does involve the interrelation of motor configuration and propellant properties and because these inter-actions are not completely understood, it is not always possible to specify propellant or chamber design procedures which will guarantee stable burning.
Presently the primary problem in the use of smokeless propellants is combustion instability. For many years the use of -' 20 high percentages of aluminum in solid propellants almost completely I inhibited combustion instability. The removal of aluminum to make the primary exhaust smokeless causes the propellant to exhibit unacceptable tendencies toward unstable combustion.
Ob~ects and Summary of the Invention ~,1 j~ It is therefore an ob~ect of the invention to provide "l ;~ a smokeless propellant in which combustion instability is substantially suppressed.
A further ob~ect of the invention is to provide a propellant substantially free of primary smoke in the exhaust and 'I ~

~.
:~!
.'' .
i ~ 3 ~ ;-,: ' ,,, ~

. ~ .. .. . . .... . . ..

1~3906Z ~.~
exhibiting a high specific impulse and burning rate without exhibiting any combustion instability.
(C) Yet another object is the provision of an ammonium perchlorate load-ed propellan~ that is absent aluminum and which maintains combustion stability at a burning rate greater than 0.40 in/sec at a pressure of about 1,000 psia.
(C) In accordance with the invention, there is provided a stable burning, smokeless, solid propellant composition comprising a cured intimate mixture of:
a major amount of solid inorganic oxidizing salt; a minor amount of a combusti-ble, synthetic organic elastomeric hydrocarbon binder resin formed by chain extension and cross-linking of functionally-terminated liquid butadiene poly-mers; and 0.2 to 5% by weight of the composition of an additive comprising a combination of (1) a refractory metal carbide or a refractory metal oxide and
(2) particulate carbon. I~ has been discovered that the addition of small amounts of additives selected from refractory metal carbides or oxides will provide a stable burning smokeless propellant for some chamber-propellant in-teractive resonant frequencies and at a burning rate above 0.40 in/sec. When a small amount of carbon in the form of hollow, thin walled spheres, whole or broken, or flakes, is also added the regime of resonance frequencies for stable , ;
combùstion is broadened. Combustion stability for a still broader band of resonance frequencies is o~tained when a small amount of carbon powder is in-cluded with the metal carbide or oxide and the carbon spheres or flakes.
i tU) These and many other objects and attendant advantages of the inven-tion will become apparent as the invention becomes better understood by refer-ence to the following detailed description when considered in conjunction with the accompanying drawings.
tu) Figure 1 is a graph showing the firing curve for a dual thrust motor in which the booster propellant grain of the bipropellant configuration con-tains additives according to the invention; and (U) Figure 2 is a graph showing the firing curve for a propellant grain without additives in the booster grain.

.:
~4~

.~: r. , , , ,: . ' ',.''' .. ',. . ., '., ,. :: ,', : ' ' ' . ' ' ' '' ' ~03906Z
Descrip~ion of the Preferred ~mbodiments The propellant composition usuially contains a high proportion of combustible solids, typically in excess of 65% by :~ weight, a small proportion of binder, usually below 15% by weight, and a small a~ount below 3% by weight of burning rate accelerator.
The combustible solids usually comprise an oxidizer such as ammonium perchlorate, HMX or RDX and 0.2-5% by weight of the combustion stisbilizing solid added in accordance with the invention.
Pre~erred binders are elastomeric hydrocarbon polymers formed by the chain extension and cross-lin~ing reactions of functionally terminated liquid polybutadiene polymers. Such polymers may include carboxy-terminated polybutadiene cured with amines or epoxides, polybutadiene acrylonitrile-acrylic terpolymers cured with epoxides and hydroxy-terminated polybutadiene cured with ;' diisocyanates. Hydroxy-terminated polybutadienes are preferred due to cost, reactivity, availability considerations and mechanical properties. The butadiene may be derived from the lithium initiated polymerization (Li-HTPB) or free radical initiated polymerization (FR-HTPB). - -~i 20 The composition may also contain a minor amount below "
10% of various additives such as cure promoters, stabilizers and ,~ thixotropic control agents, or reactive polymeric modifiers such ~
.I as one or more diols or polyols. The isocyanate is generally ~`
I present in at least an equivalent amount sufficient to react with i the hydroxy prepolgmer and hydroxyl substituted modifiers.The equivalent weight of the liquid prepolymer is at least 1,000 and not usually more than 5,000. The functionality of ' the polymer is advantageously from about 1.7 to about 3.0,preferably from about 1.9 to 2.3 to form by cross-linking and chain ,~
! ~ 30 extending elastomeric po~ymers of molecular weight of at least ;:
., .... .
.~

1~3906Z
30,000, Since higher molecular wei~ht prepolymer6 m~y re~uire heat to reduce viscosity, the ~olecular weight is preferably from ~;
1,000 to 4,000.
The polyisocyanate for curing the prepolymer can be selected from those of the general formula R(NCO) in which R
is a di- or polyvalent organic radical containing from 2-30 carbon atoms and m is 2, 3 or 4. R can be aIkylene, arylene, aralkylene or cycloalkylene. It is preferred that the organic radical be essentially hydrocarbon in character although the presence of unreactive groups containing elements other than carbon and hydrogen is permissible as is the presence of reactive groups which are not capable of reacting with isocyanate groups capable of ; forming urea or carbamate linkages such as to interfere with the desired reaction.
Examples of suitable compounds of this type include benzene-1,3-diisocyanate, hexane-1,6-diisocyanate, toluene-2,4-diisocyanate (TDI), toluene-2,3-diisocyanate, diphenyl-methane-; 4,4'-diisocyanate, naphthylene-1,5-diisocyanate, diphenyl-3,3'-dimethyl-4,4'-diisocyanate, diphenyl-3,3'-dimethoxy-4,4'-diisocyanate, butane-1,4-diisocyanate, cyclohex-4-ene-1,2-diisocyanate, benzene-1,3,4-triisocyanate, ~aphthylene-1,3,5,7-tetraisocyanate, ~ -metaphenylene diisocyanate (MDI), isocyanate terminated prepolymers, polyaryl polyisocyanates and the like.
Polyols are preferably, but not limited to, diols or triols and can be either saturated or unsaturated aliphatic, aromatic or certain polyester or polyether products. Exemplary compounds include glycerol, ethylene glycol, propylene glycol, neopentylglycol, ~entaerythritol, trimethylolethane, glycerol ' triricineolate, or alkylene oxide adducts of aniline such as Isonol*
~; :
which is ~,N-bis-(2-hydroxypropyl) aniline and many other polyols ~

~', '' ' .
*Trademark , ................................... --~03g~6Z
well known in the art which can be incorporated into the binder composition to control the degree of cross-linklng. The particular compound and amount utilized is dependent on the functionality and nature of the hydroxyl terminated prepolymer and polyisocyanate employed in the binder composition.
(U) Since the functionality of Li-HTPB is generally slightly less than 2, the polyol is preferably a triol so as to provide cross-linking between polymeric chains upon reaction with isocyanates. As exemplary polyols, mention may be made of glycerol triricinoleate (GTR0) and Isonol (a propylene oxide adduct of aniline), N,~-bis-(2-hydroxypropyl)-aniline. The polyisocyanate is present in an amount necessary to satisfy stoichiometry, that is, the functionality of the HTPB and any other polyol present in the composition. The polyisocyanate may be a di-, tri- or higher functional material and may be aliphatic in nature such as ~i hexane-diisocyanate but is preferably an aromatic polyisocyanate l such as TDI. A catalytic cure promoting agent can be utili~ed.
:! These agents may be metal salts such as metal acetylacetonates, , pre~erably thorium acetylacetonate (ThAA) or iron acetylacetonate (FeAA).
(C) The combustion stability promoting additives in accordance with the invention are used in combination at con-centrations as low as 0.2%. While no upper limit is theoretically I non-functional, however, with respect to degradation of performance and optimum exhaust smoke characteristics, the concentration of the solid additives should preferably not exceed about 3~ by weight of the propellant composition. The refractory metal carbide or oxide should have a melting point of at least about 2,000 C.

y :' : .~ ~,, , . -. . .. ,. .. , . . -. ~,.. . . ... . .

1039~6Z
~C) Suitable high meltin~ materials are the carbides and oxides of metals including thorium, tungsten, silicon, molybdenum, aluminum, hafnium, vanadium. The refractory compound should be provided in the form o~ fine particles ranging between 2 to 10 microns. The use of carbon in refractory metal compounds such as zirconium carbide will have a minimal affect on smokeless performance. Carbon will, of course, burn completely to CO and C02 while zirconium carbide at a level of 0.5% will produce about 0.7g of solid ZrO2 per lOOg of propellant burned. Smoke measurements ; lO made on firings of a propellant formulated with additive and one formulated without showed that the light transmission through the exhaust plume to be the same for both propellants, demonstrating that the ZrC had no measurable effect on the amount of primary smoke produced.
(C) It is believed that both the carbon and ZrC function through a particulate damping mechanism. Further, the carbon and ZrC represent two different classes of ~aterial. One functions ` as a particulate damper close to the burning surface. Carbon iscompletely consumed in the combustion process and cannot act to provide particulate damping the entire time the gas is present in the motor. The other, ZrC, is a particulate which is present -`
in the gas phase either as ZrC or ZrO2, most probably as ZrC.
(C) The carbon additive when utilized in combination with the refractory oxide or carbide can have diverse physical form and size.
However, when the carbon is utilized alone as a combustion - stabilizer, it should preferably have a thickness between 1 and about 10 microns and a length of between about 25 to 400 microns.
A preferred form of carbon is small particles such as platelets or spheres or carbon powder such as Thumax* (0.3~). When in the form of flakes or platelets, the preferred sizes are lO to ' 150 ~ x l to 8 ~ thick.
: . :
*Trademark : .

10~
(C) Unbroken spheres provide improved effectiveness with respect to broken spheres, eliminating an instability appearing at 2200 Hz. Elimination of frequencies above 5,000 Hz is provided by the further addition of carbon powder to the composition.
(CJ Carbon spheres that have been found effective in the invention are the following grades of carbon spheres described below produced by Kureha Chemical Industry Company, Ltd., ~okyo.
(C) Table 1 .

Property A-100 A-200 App. mean diameter, microns 110 200 Diameter range, microns 75-150 150-250 Wall thickness, microns 2-3 3-8 ; Bulk Density, g/cc 0.10-0.25 0.07-0.20 Particle density, g/cc 0.15-0.40 0.15-0.35 (C) Theoretically, the burning rate of a propellant is depen-dent only on the chamber pressure. Actually it is also dependent on ; the velocity of gas flow over the burning surface. The higher the gas ; velocity across the point on a grain, the higher the burning rate at that point. Some propellants are more susceptible to erosive burning than others. In general, erosive burning is more prevalent in lower burning rate propellants than in those with high burning rates.
(C) Unstable burning is a phenomena common to all propellant systems yet not to all propellants within a system. Furthermore, additives which in one system may control combustion instability may have no affect or an adverse affect in another propellant or binder system. It appears that unstable burning is more common with higher energy propellants than with lower energy propellants. Tests have indicated that unstable burning is a result of the production of transverse or longitudinal acoustical oscillations of the -combustion gases during burning. These oscillations result in '.

, _ g _ '' , .

1039~
(C) areas of high and low velocity around or along the grain which have a marked effect on the local burning rate. At a high velocity area caused b~ oscillation of the gas, the burning rate rises rapidly, causing a further increase in pressure. At a low velocity or nodal point, the burning rate is ~ery low. It may be seen that the non-uniform burning of the grain can cause premature break-up even if the average chamber pressure does not exceed the maximum chamber design pressure. Extremely uncontrolled performance and chamber failures are commonly associated with aggravated, uncontrolled resonance or unstable burning, although in some rockets it can be detected only by high frequency instrumentation. It appears that erosive and unstable burning are related phenomena.
(~) Combustion instability of the candidate smokeless ~i propellants in accordance with the invention was studied in a "T"
burner which is a standard device for experimental measuring of combustion instability. The "T" burner device uses opposing cylindrical grains and is usually operated at pressures of 500 and 1,000 psi. The chamber length was varied to provide fundamental acoustic frequencies near 3,000 and 4,000 Hz. The tests were ;
utilized to determine the following parameters:
~ growth constant for acoustic pressure ,~ g ~P = amplitude of acoustic pressure oscillations Rb = response function, ratio of burning rate change to pressure change I (U3 Cylindrical grains were formulated with 12 parts of an , ~
hydroxy-terminated polybutadiene binder system containing a stoichiometric amount of TDI and an appropriate amount of ammonium perchlorate and different additives. The composition was formed into cylindrical grains suitable for the "T" burner test and the ;-results of the test are provided in the following table.

: , ~03go62 ~

P~ I ~ N
V V V V V V
a) N I R .8 R R .4 .4 R
. P- la 0 ,g 1~ 0 0 0 ~l1 . O <
~ t~
o ¦ Il') ~N 11') ~D ~ _I ~r a) ~ o u~
rl t~
C~ O _l O O O
O ~ ~1 0 ~ ~D V U'~
I~') ~1 'Jl ~N r~1 1` ~r . . ~ ~ ~ ~ N U~
t~4 ~
.
1: P~ O U) O O O
<31 ~
N
t~ ~
u ~r 1` 1 ~0 u~ In ~7 U~
~1 R
' ' E~ ,01 O ~
' ~ O ~ OD 11 . o ~ u~
o " .,1 _1 . ' ~. , In O O O In u~U~
d ,', . ~ O O O ~ 1 0 0 . g ~ o , ~ a R

1,, a~ ~ ~ ~ o~ .
::~` ~ ~ ~ ~ ~ 0~ ~ 0~ 0 E~ æ ~ ~ m ~
,, _~ .

. . .
.,, ~.
o Z; ~1~N ~ er Ul ~D 1` 00 i~ ' X
.. . .

~ .
;~

(C) The higher burning rate propellant without additives, Example No. 2, is more unstable at 3,000 Hz, i.e., higher g ~P and Rb. The propellants containing broken carbon spheres (Example 5) or zirconium carbide (Example a~ or these additives in combination (Example 7) eliminate the instability at 3~000 Hz and above with some benefit obtained at 2,000 Hz, particularly in the reduced response function (Rb). Formulation No. 6 including a standard amorphous, rubber grade of carbon black, P-33, shows some reduction of the instability at 3,000 Hz but is not as effective as the carbon in the form of broken, hollow spheres (Example 5).
(C) This decrease in combustion instability shown in "T"
burners has been verified in motor firings of a dual thrust con-figuration where a booster grain composed of 88% ammonium perchlorate (AP) in an HTPB binder with 0.5% of the zirconium carbide (ZrC) was used. Although some instability was observed as shown by the DC ?
shift, this shift was only 10% of that shown by the propellant without additive. Further, the onset of the shift was delayed until the end of the boost phase.
(C) A second motor was fired using the combination of 0.5%
~ 20 ZrC and 0.5% partially broken carbon spheres, formulation No. 8 ; above, in 'che booster propellant. The results were even better with the second motor. The DC shift was eliminated entirely, leaving a residual pressure coupled maximum amplitude of only 10 psi at the ;~
operating pressure of 1,200 psi. This minor instability is well within acceptable operation limits for solid rocket motors. The firing curve for this dual thrust motor is shown in Figure 1, where formulation ~o. 8 was used for the boost phase of the operation.
Figure 2 typifies the performance of the composition without 1 additives showing the large pressure spikes resulting from com- -Oustion instability.

.

~03906Z
(C) Further "T" burner date were obtained on the effect of 1% ZrC (no carbon) on stability of the same propellant used for evaluating the 0.5% mixture with carbon and also on the ePfect of using a lower percentage of ammonium perchlorate as a lower burning rate propellant. The results are shown in the following table.

,., , , ; .......... . -.. .. . . .

~ ~039~116Z

~ .4 R R ~ R R.q .4 O
a~
P.

o C~ o o o o o o o o o o o o o o t~l N ~D ~ u~ D ~

., .
.~ . .,~
'I o 0 :~ ~O O~ er ~r ~ u~
:~ . oU~ U~ U~ U) ao . . . . .
.,~ .. 0 0 0 0 0 0 h ~
.1 i, .q dPIO u~
d ~ . . . . .
. 3 -I 0 0 0 0 0 ., ., ~ ~ . .
., .1 ~rl . ~ U~
P~
O ~ ' ~1 a ~ ~ ~ , U O C.) R C
~ ~ h E~ ~ a~ N

''I .

~l ~ ~ o Z

:i `.` --14--.:

1~39~6Z

(C) The data given in the above table shows that 1% ZrC
(Example No. 9) is equivalent in pexformance to the propellant containing the mixture of additives (Example No. 7). The use of eome carbon is considered significantly superior since it does not S create any particulate smoke. The firings of the propellants of Examples No. 10 and 11 were both stable until the ratio of Sb/S~O
was 1 or less and then the firing became unstable. Sb indicates the area of the propellant burning and SCO is the cross-sectional area of the chamber. The lower burning rate propellant containing a lower amount of ammonium perchlorate as shown in Example No. 12 shows that with this composition stability is improved, being stable at 2200 and 2600 Hz. Further "T" burner data is shown in the following table.

:
~', '' .

.

, ~ .
:,. .

`, --15--;

':

~03~06Z
,, .
'.a~ ~1 ~ ,.

C ~ P.~ a n ~ ~
o o 01 N ~ O O o .~ ¦ ~ N N
Ul ~
V V V V
N I O .a .4 .~ .q ' oo P~
~ u . ~ ~U~ N
I V V
N
P~ I` O U~ O OD Ul O cl ~ O

¦ O ~ co ~ I N
cl ¦ ~ N
N ca 1 . ~q 1~

~1 = ~ o o lo ~ l . , E~ `1 I J
. u~ p o ~d ., ' ' . ~ D N017 r~ I ~I CO ~n ~ o O O O C, O O O O O O O Cl Cl' ., O O O O
C~ ' :~ ~U C i~
; .q g .~ .c .~ .c .c .c ' P~

'1 . ~, ., , ~ r~ o ` 1 1~ Z; _I _11 rl ~1 ~. _I ~1 N N N N N
.'~ . 1l1 ., . ~ :
.;~ .
.:' .'~ .

~03~06.;i~
,.
."
. ~ ~ P ~ o o o o `
V J~
o o u~
~ ~ ~1 .
.
, . :. .

. .. ..
N p~
~0 , U~ , , ' , . ., ' ' ' , .
, ~ ' ~ , ' ' ' . ' ' d ~
,,p p Pl ~r ' '- ' , . _ o o . , .
.' ~''' o ~ ~ ' , '' ':- ' u . . a~ o 1~
, E~ . t~ j .
.. . , ., .
' ' ~
. . d u ~o oooooooo~o ., ~qrl ' dP OO O O O o o O O ' . oo o o o o o o o U U~ ,U U ~ P~
t~ N N
N q) h ,~ O
. ~ .~ ~ N N
; ~ ~ ~P- U C~ U U o dP o o ~P 1 ; O ~D

.' ' ' ~U . ~ . .
~ ~ O
.az . . . ..

.

103gO6Z

(C) The control propellant batches 17 and 18 show that without additives all AP propellants are unstable at 2000 and 3000 Hz although stabilized at a frequency of 4000 Hz. It iB evident that at higher burning rate, i.e. batch ~o. 18, instability is increased at 3000 Hz.
(C) The effect of various forms of carbon is seen in batches 14, 29, 13 and 15. Neither P-33 (Example 14~ nor carbon fibers (Example 15) gave an improvement in stability at 87% AP. Carbon spheres A 100 (Example 13) gave improved stability at 87% AP and 3000 Hz. At 88% AP, carbon spheres gave improved stability at both 3000 or 4000 Hz.
(C) Zirconium carbide (Example No. 16) gave significantly ~-~
improved stability at 3000 and 4000 Hz. Additional testing of carbon spheres, 1%, and ZrC, 0.5%, as single additives in the "T"
burner and also in motors (Examples 19, 20 and 21) showed these ; compositions to be unstable in the "T" burner at 2500 Hz. Motor firings of Example 21 also showed these compositions were unstable ;
.:
when the propellant web burned out to a diameter corresponding to ;, a frequency of 4000 at 5000 Hz. -`ll 20 (C) In combination the ZrC and carbon spheres (Examples 25, ;
' 19, 26, 23 and 24) gave stable combustion in the "T" burner at :.' `. -: .: :
2500 Hz and were also stable in 9-in O.D. grains, when fired in , motors having a frequency at burnout of 2700 Xz. The effect of -,l~ the combination produces an improvement in stability over that ,~
shown by the single ingredients when used alone.
(C) A further evaluation of the effect of carbon and ZrC
was tested in Example Nos. 27, 28 and 29 which showed that both car- ~
bon powders as well as spheres provided improved stability at 2600 ~ -Hz although all combinations were unstable at 2200 Hz. The amor-phous blacks were stable in the "T" burner even at Sb/Sc ratios . ' ,:
` - 18 -~03.9l~
(C) as low as l, the ratio of the area of propellant burning surface to the area of the cross-sectional chamber~ whereas the propellant with carbon spheres with ZrC was unstable at this area ratio.
Although this instability was evident in "T" burners, no instability was seen in motor firings evidently because at an Sb/SCO ratio of l the grains are burning as flat slabs and have no contribution from side wall burning as is the case in a typical ID burning grain configuration. The results show that stability above 2500 Hz is primarily due to the combination, carbon plus ZrCg and is not dependent on the form of carbon.
(U) The experiments summarized in Table 5 show the compar-ison of "T" burner results at 900 and 2500 psia with full scale motor tests conducted at 900-1500 psia and 70 F. The binder in each example was a plasticized HTPB.

~ 3~
(C) as low as 1, the ratio of the area of propellant burning surface to the area of the cross-sectional chamber, whereas the propellant with carbon spheres with ZrG was unstable at this area ratio.
A]though this instability was evident in "T" burners, no instability `
was seen in motor firings evidently because at an Sb/S~O ratio of 1 the grains are burning as flat slabs and have no contribution from side wall burning as is the case in a typical ID burning --grain configuration. The results show that stability abo~e 2500 Ez is primarily due to the combination, carbon plus ZrC, and is not dependent on the form o~ carbon.
(U) The experiments summarized in Table 5 show the co~par- `~
ison o~ "T" burner results at gO0 and 2500 psia with full scale motor tests conducted at 900-1500 psia and 70 F. The binder in each example was a plasticized ~TPB. -~

, ;: : .

~ . '' :' ~,`,'.''' .,' '' '.~ ` '"' .: ~ . `
i` ` ~

:, :

~0~ 6Z

U~ ~ ~ ~
0 ., C~
~ .~ .q ~ ~ ~
~ ~ o I~ u~
o .
. . X
6, o o C~
o o ~ ~ ~ o~
,, ~ . ,.

G~
P ~ C~l E~
N N

00 ~ O ~ O

~ ~ ~ I
J ~ 0 ~ O U~ ~ ~ ~ U~ u~ , . .
E ~ ~ ~ ~ o O
111 t ~
' 0 ~
~ ~ ,~
~ .,~ - .

;~ ~ l ~ fi N o o o o ~ o ~0 ~ O O
I'~
.
. . ~ :
~ V ~) h V

cP n ., . . co co ~ , . ~
. o r~
. . 0 X ~ , C~l W , , .
.. , . . '' ~039~6Z
(C) The correlation between motor diameter and motor resonant frequency is shown in the following table:

Table 6 Motor Diameter, Motor Resonant D, inch Frequency, cps 4.0 6,000 5,0 4,800 6.0 4,00p 7.0 3,430 8.0 3,000 9-0 2~670 1~.00 ~400 "

, ., .

(C) The data in Table 5 shows a good correlation between the results obtained with "T" burner and the motors. This is par-ticularly evident for Example No. 47 where the "T" burner showed stability at 2600 Hz a~ did the motor at 2690 Hz, while the "T"
burner showed instability at the lower fre~uency o~ 2200 Hz.
(C) Example No. 36 (89% AP, r , 0.~1 in/sec at 1000 psia) containing no additive was unstable both in the "T" burner at 2500 Hz and in the motor at even a higher frequency of ~4000 Hz.

(C) Example No. 37 (o8% AP, 0.5% Ee2o3~ r s 0.59 in/sec at 1000 psia) again was unstable at a hieher frequency in the motor indicating the effect of higher burning rate on the instability.
(C) Example No. 38 (87% SP, r ~ 0.49 in/sec at 1000 psia) contained 100~ carbon spheres and 5~ ZrC and was found to be stable both in the "T" burner and in the motor firing down to 4800 Hz, illustrating the effect of the combination of additives.
(C) Example No. 39 (87% AP, r _ o.54 in/sec at 1000 psia) contained 200~ carbon spheres and 5~ ZrC and was Pound to be stable in the "T" burner illustrating that 200~ carbon spheres are as ~ -effective as the lO0~ spheres.
(C) Example No. 40 (88% AP, r = o.56 in/sec at 1000 psia) contained only 0.5% ZrC and was found to be unstable in the "T"
burner and at ~5000 Hz in the motor illustrating the need for the carbon spheres for stability.
(C) Example No. 41 (87% AP, r _ 0.53 in/sec at 1000 psia) contained 1% of 200~ carbon spheres and was found to be unstable in the "T" burner illustrating the need for the ZrC in combination.
(C) Example No. 42 (88% AP, 4 = 0.41 in/sec at 1000 psia) contained 1% of 200~ carbon spheres and was found to be unstable in the "T" burner and in the motor at ~4, ooo ~z illustrating again the need for the combination to achieve stability.

.,,.. . . . . ::
.. . .

1C~3~06;~
(C) The remaining batches illustrate the ef~ect of the combination of carbon spheres and ZrC. Both the T burner and motor results show the effectiveness of the combination of additives in achieving stability over the range of burning rates from ~0.~0 to ~o.60 in/sec at 1000 psia at frequencies as low as 2500 Hz and an oxidizer level from 87 to 88%. At the burning rates above o.60 in/sec at 1,000 psia instability at 2500 Hz was evident in the T
burner. Stability in motors was maintained over the temperature range of -40 to +135F as shown by the motor fired from Example `
~o. 47. -(C) Thus it is apparent that solid additives such as a refractory metal carbide alone, irregular thin carbon particles such as broken carbon spheres or the combination of refractory metal compound with diverse forms of carbon are capable of provid-ing stable burning, high energy, smokeless propellants without significant loss of specific impulse even though aluminum has been eliminated from the fuel.
(C) A further series of T burner date for propellants containing other refractory compounds such as 0.5 weight percent of hafnium oxide, niobium carbide or tantalum carbide in combina-tion with 0.5 weight percent of 200 micron diameter carbon spheres and 87% ammonium perchlorate (AP) is presented in the following table.

~3~(~6~:
.., U~
P o U~ o o o C~
U~ I~
r- ~9 P.

U
,, o ,, ,, ,, .~
~,q R u~ Q R .Q er ~i 0 + ~ ~ ~ +
~ tn u~

tJ` O
~: O
~ ~ W O O
o o o o o U~
O `
H
~4 ~¢
~ U q~ o o o o o o O ~ o o o o o o 0 ~ ~D ~ ~ N ~D ~
~0 o ~J ~ ~1 C~l t'~l ~1 ~ , .
~a ~Q
t` ~ ~

E~a~ ~ ~ r o ~-~ 00 ~ C2 ~D ~ O
O O O O O
h r-~ ~1 --I ~ 'I
Pl a) , .
1) P
~ O O ~ ~ O O S
.,1 ~ ~ R ,Q
~ W 1 Z Z E~

a).
Q. O c~ a~ o _ I

Z
~ .
, ~3~06;~ `
~ , propellant was compounded as follows:
.
Ingredient Wt.%
AP . 87 -Carbon Spheres (unbroken) 0.5 Carbon Powder 0.5 Zircon;um Carbide. 0.5 sinder of Example 1 ll.S

(U) Forty-two pounds of the propellant was fired in a full scale motor. The motor developed 4,000 to 8,000 pounds of thrust and was found to be absent frequencies above 5,000 Hz.

~039C~
(C) Propellant compositions absent the additives of the invention do not burn stably unless the ammonium perchlorate level is below 80% by weight. This lowers both the impulse and density of the propellant. The propellant composition ~f the invention containing the stabilizing smokeless additives permits formulation with over 85% ammonium perchlora~e to form a high density solid propellant which burns stably with high specific impulse and without visible smoke.
(U) It is to be realized that only specific embodiments of the invention have been described and that numerous substitutions, alterations and modifications are all permissible wi~hout departing from the scope of the invention as defined in the following claims.
.

.

Claims (15)

THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A stable burning, smokeless, solid propellant composition comprising a cured intimate mixture of: a major amount of solid inorganic oxidizing salt;
a minor amount of a combustible, synthetic organic elastomeric hydrocarbon binder resin formed by chain extension and cross-linking of functionally-ter-minated liquid butadiene polymers; and 0.2 to 5% by weight of the composition of an additive comprising a combination of (1) a refractory metal carbide or a refractory metal oxide and (2) particulate carbon.
2. A composition according to claim 1 in which the binder resin is pre-sent in an amount of not more than 15% by weight and the additive is present in an amount from 0.2 to 3% by weight.
3. A composition according to claim 2 in which the binder resin is a chain extended and cured liquid polybutadiene polymer having an equivalent weight between 1,000 and 5,000 and a functionality between 1.7 and 3Ø
4. A composition according to claim 3 in which the oxidizing salt is ammonium perchlorate present in an amount of between 85% and 90% by weight.
5. A composition according to claim 4 in which the additive comprises 0.2 to 1% by weight refractory metal carbide having a melting point of at least about 2000°C and a particle size ranging between 2 to 10 microns.
6. A composition according to claim 5 in which the refractory metal carbide is a carbide of a metal selected from the group consisting of thorium, tungston, silicon, molybdenum, aluminum, hafnium and vanadium.
7. A composition according to claim 6 in which the carbide is zirconium carbide.
8. A composition according to claim 6 in which the carbide is hafnium carbide
9. A composition according to claim 6 in which the additive comprises a mixture of a refractory metal carbide and particulate carbon.
10. A composition according to claim 9 in which the particulate carbon is selected from hollow, thin-walled carbon spheres and carbon flakes.
11. A composition according to claim 10 in which said additive further includes carbon powder.
12. A composition according to claim 3 in which the additive consists essentially of particulate carbon having a thickness between 1 and 10 microns and a length between about 25 and 400 microns.
13. A composition according to claim 12 in which the particulate carbon is in the form of flakes having a thickness from 1 to 8 microns and a length from 10 to 150 microns.
14. A composition according to claim 12 in which the particulate carbon is in the form of hollow carbon spheres having a diameter between 100 and 200 microns and a wall thickness from 2 to 8 microns.
15. A method for producing thrust in the absence of smoke comprising the steps of:
burning a solid propellant composition defined according to claim 1 at a burning rate above about 0.4 in/sec without combustion instability at pressures of at least 1000 psia so as to produce non-smoking combustion gases; and exhausting said gases through an orifice to produce thrust.
CA201,806A 1973-06-07 1974-06-06 Smokeless stable burning propellant Expired CA1039062A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US360867A US3924405A (en) 1973-06-07 1973-06-07 Solid propellants with stability enhanced additives of particulate refractory carbides or oxides

Publications (1)

Publication Number Publication Date
CA1039062A true CA1039062A (en) 1978-09-26

Family

ID=23419724

Family Applications (1)

Application Number Title Priority Date Filing Date
CA201,806A Expired CA1039062A (en) 1973-06-07 1974-06-06 Smokeless stable burning propellant

Country Status (11)

Country Link
US (1) US3924405A (en)
JP (1) JPS5214285B2 (en)
BE (1) BE816054A (en)
CA (1) CA1039062A (en)
DE (1) DE2427480C3 (en)
FR (1) FR2232523B1 (en)
GB (1) GB1465804A (en)
IL (1) IL44980A0 (en)
NO (1) NO139916C (en)
SE (1) SE404359B (en)
TR (1) TR18072A (en)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1506185A (en) * 1975-06-11 1978-04-05 Bryant & May Ltd Match-head compositions
US4084992A (en) * 1976-04-22 1978-04-18 Thiokol Corporation Solid propellant with alumina burning rate catalyst
US4061511A (en) * 1976-08-02 1977-12-06 The United States Of America As Represented By The Secretary Of The Navy Aluminum silicate stabilizer in gas producing propellants
US4158583A (en) * 1977-12-16 1979-06-19 Nasa High performance ammonium nitrate propellant
GB2193491B (en) * 1978-07-21 1988-09-14 Imi Kynoch Limited Kynoch Work Improvements in propellants
FR2538378A1 (en) * 1982-12-28 1984-06-29 Poudres & Explosifs Ste Nale NOVEL COMBUSTION INHIBITORS BASED ON POLYURETHANE OXYGEN ELASTOMER COMPRISING FIBERS FOR DOUBLE-BASED PROGERGOLS
FR2564457B1 (en) * 1984-05-17 1986-09-26 Poudres & Explosifs Ste Nale COMBUSTION INHIBITOR BASED ON ALIPHATIC POLYURETHANE ELASTOMER FOR PROPERGOL, AND BLOCK COATED WITH THIS INHIBITOR
GB2159811A (en) * 1984-06-06 1985-12-11 Alan Richard Howard Bullock Composite propellant
US4574700A (en) * 1984-11-15 1986-03-11 The United States Of America As Represented By The Secretary Of The Air Force Solid rocket motor with nozzle containing aromatic amide fibers
US5867981A (en) * 1985-01-28 1999-02-09 The United States Of America As Represented By The Secretary Of The Air Force Solid rocket motor
DE3523953A1 (en) * 1985-07-04 1987-01-15 Fraunhofer Ges Forschung METHOD AND DEVICE FOR PRODUCING SOLID FUELS
JPS62263409A (en) * 1986-05-12 1987-11-16 Emupaiya Eapooto Service:Kk Encoder
JPS62276409A (en) * 1986-05-26 1987-12-01 Emupaiya Eapooto Service:Kk Rotary encoder
DE3704305A1 (en) * 1987-02-12 1988-08-25 Bayern Chemie Gmbh Flugchemie COMPOSITE SOLID FUEL
US5074938A (en) * 1990-05-25 1991-12-24 Thiokol Corporation Low pressure exponent propellants containing boron
US5334270A (en) * 1992-01-29 1994-08-02 Thiokol Corporation Controlled burn rate, reduced smoke, solid propellant formulations
US5339625A (en) * 1992-12-04 1994-08-23 American Rocket Company Hybrid rocket motor solid fuel grain
US5445690A (en) * 1993-03-29 1995-08-29 D. S. Wulfman & Associates, Inc. Environmentally neutral reformulation of military explosives and propellants
US5547525A (en) * 1993-09-29 1996-08-20 Thiokol Corporation Electrostatic discharge reduction in energetic compositions
US5470408A (en) * 1993-10-22 1995-11-28 Thiokol Corporation Use of carbon fibrils to enhance burn rate of pyrotechnics and gas generants
US5438824A (en) * 1994-03-21 1995-08-08 The United States Of America As Represented By The Secretary Of The Army Silicon as a high energy additive for fuel gels and solid fuel-gas generators for propulsion systems
DE4435524C2 (en) * 1994-10-05 1996-08-22 Fraunhofer Ges Forschung Solid fuel based on pure or phase-stabilized ammonium nitrate
DE4435523C1 (en) * 1994-10-05 1996-06-05 Fraunhofer Ges Forschung Solid fuel based on phase-stabilized ammonium nitrate
JPH08231291A (en) * 1994-12-27 1996-09-10 Daicel Chem Ind Ltd Gas generating agent composition
US5834680A (en) * 1995-09-22 1998-11-10 Cordant Technologies Inc. Black body decoy flare compositions for thrusted applications and methods of use
WO1999018049A2 (en) * 1997-10-03 1999-04-15 Cordant Technologies, Inc. Advanced designs for high pressure, high performance solid propellant rocket motors
US6217682B1 (en) * 1997-10-27 2001-04-17 Cordant Technologies Inc. Energetic oxetane propellants
US6168677B1 (en) * 1999-09-02 2001-01-02 The United States Of America As Represented By The Secretary Of The Army Minimum signature isocyanate cured propellants containing bismuth compounds as ballistic modifiers
US6607617B1 (en) 2000-08-16 2003-08-19 Alliant Techsystems Inc. Double-base rocket propellants, and rocket assemblies comprising the same
US11434181B2 (en) * 2013-03-15 2022-09-06 Northrop Grumman Systems Corporation Precursor formulations for a propellant composition including high surface area amorphous carbon black

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2926613A (en) * 1955-05-23 1960-03-01 Phillips Petroleum Co Composite rocket-ram jet fuel
US2995429A (en) * 1956-03-26 1961-08-08 Phillips Petroleum Co Solid composite rubber base ammonium nitrate propellant cured with metal oxide
US3822154A (en) * 1962-10-01 1974-07-02 Aerojet General Co Suppression of unstable burning using finely divided metal oxides
US3666575A (en) * 1970-03-10 1972-05-30 Us Army Solid propellant composition with burning rate catalyst
US3734786A (en) * 1971-02-16 1973-05-22 United Aircraft Corp Solid propellants fabricated from a mixed polymer system

Also Published As

Publication number Publication date
SE404359B (en) 1978-10-02
JPS5031015A (en) 1975-03-27
FR2232523A1 (en) 1975-01-03
TR18072A (en) 1976-09-21
BE816054A (en) 1974-09-30
NO742028L (en) 1975-01-06
DE2427480B2 (en) 1979-04-26
FR2232523B1 (en) 1977-09-30
DE2427480C3 (en) 1979-12-13
SE7407489L (en) 1974-12-09
NO139916B (en) 1979-02-26
JPS5214285B2 (en) 1977-04-20
GB1465804A (en) 1977-03-02
NO139916C (en) 1979-06-06
US3924405A (en) 1975-12-09
IL44980A0 (en) 1974-09-10
DE2427480A1 (en) 1975-01-09

Similar Documents

Publication Publication Date Title
CA1039062A (en) Smokeless stable burning propellant
US5074938A (en) Low pressure exponent propellants containing boron
US3144829A (en) Solid propellant charge
US5619011A (en) Process for producing a hybrid rocket fuel
KR20010079983A (en) Castable double base solid rocket propellant containing ballistic modifier pasted in an inert polymer
US4263071A (en) Additive for reducing combustion instability in composite solid propellants
US4057441A (en) Solid propellant with burning rate catalyst
Kohga From cross‐linking to plasticization–characterization of Glycerin/Htpb blends
US3086895A (en) Solid composite propellant containing acetylenic polyurethane and process of making
US2995430A (en) Composite propellant reinforced with
US3908358A (en) Variable flow gas generating method and system
US2988435A (en) Ammonium nitrate gas-generating compositions
US4239073A (en) Propellants in caseless ammunition
AU759600B2 (en) Hydrazinium nitroformate based high performance solid propellants
US2936225A (en) Ammonium nitrate propellant
US2991166A (en) Propellant and gas producing compositions of elastic gels containing inorganic oxidizing salts
US2962368A (en) Table
US3154449A (en) saucxuc acid
US2973256A (en) Ammonium nitrate solid composite propellant composition
US3000718A (en) Propellant compositions
US3148096A (en) Ammonium nitrate gas generating composition with combustion catalyst
US4201605A (en) Gas generator propellant for airbreathing missiles
KR102633762B1 (en) Insensitive smokeless solid propellant composition comprising N-Guanylurea dinitramide
US3153603A (en) Ammonium nitrate combustion catalyst
JP3781821B2 (en) Gas generant fuel