[0001] The present invention is directed to castable thermoplastic binders for high-energy
compositions, particularly composite solid rocket propellants.
BACKGROUND OF THE INVENTION
[0002] Conventional solid composite propellants utilize chemically cross-linked elastomers
in which prepolymers are cross-linked by chemical curing agents. As outlined in detail
in U.S. Patent No. 4,361,526, there are important disadvantages to cross-linked elastomers.
Cross-linked elastomers must be cast within a short period of time after addition
of the curative, which time period is known as the "pot life". Disposal of a cast
cross-linked propellant composition is difficult except by burning which poses environmental
problems.
[0003] As an alternative to cross-linked binders, U.S. Patent No. 4,361,526 proposes to
use a thermoplastic elastomeric binder which is a block copolymer of a diene and styrene,
the styrene blocks providing a meltable crystal structure and the diene blocks imparting
rubbery or elastomeric properties to the copolymer. In order to prepare a propellant
composition using the copolymer, the copolymer is dissolved in an organic solvent,
such as toluene, and the solids and other propellant formulations are added. The solvent
is then evaporated, leaving a rubbery solid which may be divided into pellets suitable
for casting or other processing.
[0004] A disadvantage of formulating a propellant composition using a thermoplastic elastomeric
binder which must be dissolved in a solvent is that the propellant formulation cannot
be cast in a conventional manner, e.g., into a rocket motor casing. Furthermore, solvent-based
processing presents problems with respect to solvent removal and recovery. Organic
solvents, such as toluene, present certain hazards both to the immediate work area
and to the larger environment, necessitating various precautions to be taken with
respect to processing such propellant formulations.
[0005] It would be desirable to have propellants and other high-energy solid compositions
which include thermoplastic elastomeric binders which can be melted and cast without
the need for solvent processing.
SUMMARY OF THE INVENTION
[0006] In accordance with the invention, a propellant binder system comprises a high molecular
weight syndiotactic 1,2-polybutadiene binder plus a suitable plasticizer. The polybutadiene
binder system is useful for spatially immobilizing solid particulates, such as fuel
material particulates and oxidizer particulates, in a propellant formulation. The
polybutadiene binder is meltable, allowing it to be mixed with other components of
the propellant formulation, including the solid particulates and the plasticizer,
and is castable, e.g., into a rocket motor shell. No organic solvent is required to
prepare or cast the propellant formulation.
DETAILED DESCRIPTION OF CERTAIN PREFERRED EMBODIMENTS
[0007] High molecular weight syndiotactic 1,2-polybutadiene in combination with a suitable
plasticizer, is found to provide a suitable elastomeric binder system for solid propellant
compositions or the like. The polymer is a thermoplastic elastomer which melts in
the temperature range of from about 70°C to about 100°C and therefore can be melted
in the presence of fuel particulates and oxidizers to form a solvent-free propellant
formulation melt. The melt is directly castable as a propellant charge into a rocket
motor casing or the like.
[0008] Polybutadienes in accordance with the present invention have weight average molecular
weight of between about 100,000 and about 200,000. The crystallinities range from
between about 10 percent and about 35 percent and preferably between about 15 and
about 30%. Densities range from about 0.90 to about 0.91. By 1,2 butadiene is meant
that substantially all, i.e., greater than about 90% of monomer addition is by 1,2
polymerization. By syndiotactic is meant that at least about 90% of the 1,2 additions
result in the pendant vinyl group extending from the side opposite that of the two
flanking pendant vinyl groups. Syndiotactic 1,2-polybutadiene polymers suitable for
use as binders are sold, for example, by the Japanese Synthetic Rubber Company under
the trade designations JSR RB-810, JSR RB-820 and JSR RB-830.
[0009] Polybutadienes used in accordance with the present invention have thermal properties
which make them especially suitable as propellant binders, the range from the brittle
point (glass transition temperature (T
g)) to the softening point generally encompassing the ordinary ambient temperature
range. Viscat softening points of these compounds range from about 35°C to about 70°C;
melting points range from about 70°C to about 100°C and brittle points range from
about -35°C to about -40°C. Thus while the thermoplastics are elastomers at ambient
temperatures, they can be processed as molten plastics at temperatures far below the
temperatures where high-energy solids become unstable. The low processing temperatures
of 1,2 syndiotactic butadienes is considered an important advantage relative to other
thermoplastic elastomers which have been considered for use as propellant binders.
[0010] The polybutadienes have good tensile properties for binders. 300% moduli range from
about 40 to about 80 kg/cm²; Tensile strengths range from about 60 to about 140 kg/cm²
and elongation ranges from about 650 to about 800 %. Shore D hardnesses range from
about 30 to about 50.
[0011] To provide the polymer with suitable elastomeric properties to serve as a binder,
the complete binder system includes a plasticizer with which the polymer is miscible.
Suitable plasticizers include dioctyl adipate (DOA) and dioctyl phthalate (DOP); however,
other miscible plasticizers known in the art are also suitable. Mixtures of plasticizers,
such as DOA/DOP mixtures are also suitable. Particularly suitable plasticizers are
naphthenic oils, such as those sold under the trademark Tufflo by Arco, particularly
Tufflo-500. The plasticizer comprises between about 50 and about 75 percent by weight
of the binder system (binder plus plasticizer) and preferably between about 50 and
about 67 percent by weight.
[0012] The binder system may also include a minor amount of a wetting agent or lubricant,
such as lecithin. The wetting agent or lubricant enables a higher solids loading.
The lubricant typically comprises up to about 4 weight percent of the total weight
of the polybutadiene plus plasticizer. A presently preferred lubricant is a coating
agent sold under the trade designation FC-430 by 3M.
[0013] A complete propellant formulation includes a high percentage of energetic solid particulates,
including fuel material particulates, such as aluminum, and oxidizer particulates,
such as ammonium perchlorate (AP), cyclotetramethylene tetranitramine (HMX) and cyclotrimethylene
trinitramine (RDX), the solid particulates typically comprising between about 70 and
about 90 wt. percent of the propellant composition and the balance being substantially
all binder system. In addition, the propellant may include minor amounts of additional
components, such as a bonding agent and burn rate modifiers.
[0014] Because the thermoplastic elastomer does not have a "pot life" in the sense of cross-linked
elastomers, the order of mixing propellant formulation ingredients is not considered
to be critical. However, for ease of mixing, it is generally preferred that the binder
system, including the binder, plasticizer, and any lubricant, be blended under binder
melting conditions prior to adding the solids. After the binder system is melted and
blended, the solids are added, and mixing is continued to provide a uniform dispersion
of solids in binder system. To provide a uniform cast, it is preferred to deaerate
the molten formulation and then to cast the melt.
[0015] Cast propellant may be remelted after solidifying. Thus, there is no need to cast
the propellant immediately after mixing, although from an energy efficiency standpoint
this is generally desirable.
[0016] An important advantage of having a propellant which is meltable is that the propellant
from an outdated missile can be melted down and reused. At the time of such remelting,
the propellant might be reformulated, e.g., by addition of additional fuel or oxidizer
particulates. Accordingly, the thermoplastic of the propellant composition provides
for its eventual recycle, as opposed to the burning required for disposal of thermoset
propellant compositions. Because the thermoplastic propellant does not have a "pot
life", there are no limitations to the time of casting, and if any problems develop
during casting, the process can be delayed as long as necessary merely by maintaining
the propellant formulation in molten form.
[0017] In preparing propellants in accordance with the present invention, no solvents or
other highly volatile substances are required. Accordingly, no special measures or
special apparatus are required to contain solvent vapors, to remove solvent from the
formulation or to recover solvent for reuse. Propellant formulations in accordance
with the present invention may be prepared by conventional mixing apparatus without
requiring extrusion, although extrusion may be used to prepare certain forms of propellants,
such as propellant pellets.
[0018] An important advantage of syndiotactic butadienes for use in propellant binders is
their low melting temperatures, and propellant formulations using syndiotactic butadienes
are processable in the range of to 120°C. Low processing temperatures help to ensure
safety in processing high-energy compounds. Syndiotactic butadienes also have excellent
low-temperature properties, typically having glass transition temperatures in the
range of -40°F (-40°C). Low-temperature properties are important for propellant systems
which might be used at very low temperatures or even exposed to very low temperatures
prior to use.
[0019] The invention will now be described in greater detail by way of specific examples.
Example 1
[0020] A pilot scale mix of a composite propellant with a thermoplastic elastomeric binder
is described in this example. 240 grams of a composite propellant were made from the
following ingredients:
Ingredient |
Weight Percent |
Syndiotactic Polybutadiene RB-810 |
8.3 |
Dioctyl Adipate |
15.9 |
Lecithin |
0.8 |
Unground Ammonium Perchlorate (AP) 200µ |
50.0 |
Ground Ammonium Perchlorate (AP) 18µ |
25.0 |
[0021] The ingredients were mixed in a Baker Perkins twin blade vertical mixer with a working
capacity of approximately 0.5 liters. First the polybutadiene, dioctyl adipate, and
lecithin were added to the mix bowl and mixed for a total of 70 minutes with stops
after 10, 20, 40 and 60 minutes for scrape down of the mixer blades. A water/ethylene
glycol mixture at 210°F was circulated through the mixer jacket in order to heat the
mixture. After 70 minutes of mix time, the mix temperature had climbed to 160°F and
the polybutadiene was partially melted. At this point, one half of the unground AP
was added to the mix bowl and mixed for 20 minutes. After 130 minutes total of mix
time, the mixing was complete and the batch was uniform in appearance. The mix temperature
was 177°F and its viscosity was 8 Kp. The mix was then deaerated and cast into a rectangular
mold by letting it drop through a funnel and slit plate into a vacuum bell.
[0022] After the mold had cooled, the propellant was removed from it and cut into ¼ ˝ diameter
by 4˝ long cylindrical stands for testing of burn rate. Four strands were prepared
and inhibited on all but one circular face with black enamel paint. These strands
were then burned in a pressurized bomb to determine propellant burn rate. Two strands
were burned at an average pressure of 1015 psig and had an average burn rate of 0.247
in/sec. The other two were burned at a pressure of 510 psig and had an average burn
rate of 0.183 in/sec.
Example 2
[0023] Nine more pilot scale batches of composite propellants using the thermoplastic elastomer
binder were made and cast substantially the same manner as described in Example 1.
The level of AP oxidizer was varied from 75% to 85% of the total mixture by weight.
Both RB-810 and RB-820 grades of JSR syndiotactic polybutadiene were used and plasticizer
to polymer ratio was varied between 2 to 1 and 1 to 1. The table below indicates the
batch numbers, formulation and processing results for these batches. JANNAF Class
C uniaxial tensiles were prepared from the finished batches and tested at a constant
strain rate of 2.0 in/min at a temperature of 77°F. Maximum stress, strain at maximum
stress and elastic modulus were calculated from these tests and are presented in the
table.

[0024] While the invention has been described in terms of certain preferred embodiments,
modifications, obvious to one with ordinary skill in the art may be made without departing
from the scope of the present invention. For example, although the novel binder system
according to the present invention has been described primarily in terms of its use
in propellants, the binder system is applicable to other solid, high-energy compositions,
such as explosives and gasifiers.
[0025] Various features of the invention are set forth in the following claims.
1. A melt-cast propellant composition comprising energetic particulate solids dispersed
in and spatially immobilized in a binder system having between about 25 and about
50 weight percent of 1,2 syndiotactic polybutadiene and between about 50 and 75 weight
percent of a plasticizer miscible with said polybutadiene.
2. A composition in accordance with Claim 1 comprising between about 70 and about
90% energetic particulate solids, balance said binder system.
3. A composition in accordance with Claim 1 wherein said 1,2 syndiotactic polybutadiene
has a weight average molecular weight of between about 100,000 and about 200,000.
4. A composition in accordance with Claim 1 wherein said plasticizer is selected from
the group consisting of dioctyl, adipate, dioctyl phthalate and mixtures thereof.
5. A composition according to Claim 1 wherein said binder system includes up to about
4 wt. percent of a wetting agent based upon the total weight of plasticizer and polybutadiene
in said binder system.
6. A method of preparing a propellant composition comprising mixing energetic particulate
solids with 1,2 syndiotactic polybutadiene plus a plasticizer that is miscible with
said polybutadiene at a temperature whereat said polybutadiene is molten, melt-casting
said molten mixture into a mold, and allowing said molten mixture to cool to a solid
propellant composition with said solid particulates dispersed in plasticized polybutadiene.
7. A method according to Claim 6 wherein said molten mixture is deaerated before cooling.
8. A method according to Claim 7 wherein said molten mixture is cast after deaeration
and prior to cooling.
9. A method according to Claim 6 wherein said temperature is at least about 90°C.
10. A method according to Claim 6 wherein said polybutadiene and said plasticizer
are blended at said temperature and then said energetic solids are added.