Patent Grant
9828304
The present invention relates generally to aerial countermeasures and more specifically to iron/ceramic composite pyrophoric materials used as such decoys along with methods for preparation thereof.
Decoy flares are countermeasures ejected from an aircraft to mislead a missile's infrared or heat seeking guidance system to target the flares rather than the aircraft. Decoy flares may be categorized as pyrotechnic or pyrophoric. Pyrotechnic flares use a slow burning fuel/oxidizer combination to generate intense heat to attract the missiles. In contrast, pyrophoric flares self-ignite when exposed to oxygen in the air. When the pyrophoric material is ejected from an aircraft, it is designed to flutter in the air due to the high surface area to mass ratio of the pyrophoric material. This allows the pyrophoric material to disperse in a cloud like pattern thereby mimicking an aircraft's fuel exhaust or hot engine components.
Conventional methods for the preparing pyrophoric countermeasures rely on chemical leaching techniques for the formation of high specific surface area metal substrates that are reactive to oxygen. U.S. Pat. No. 4,895,609 issued to Baldi et al, discloses current methods for preparing iron coated on steel pyrophoric materials. The methods generally requires:
The Baldi method utilizes chemical leaching to prepare porous iron which requires use of high concentrations of hot, corrosive NaOH solution. Handling of such caustic materials increases safety risks to the user as NaOH has been known to cause permanent damage to human tissue. Sodium hydroxide is also designated as a hazardous environmental substance under the Federal Water Pollution Act and Clean Water Act.
U.S. Pat. No. 8,623,156 issued to Haines et al, addresses alternative methods for preparing pyrophoric foils without the use of chemically hazardous materials like NaOH. The patent discloses methods for water based processing followed by hydrogen reduction of iron oxide to form pyrophoric nano-iron on various types of ceramic, metal, and nanomaterial substrates. Similar to Baldi, the Haines' '156 patent also requires an underlying substrate to provide structural integrity to the pyrophoric material.
U.S. Patent application publication number 20060042417 by Gash et al, discloses sol-gel methods to generate high surface area porous iron for making pyrophoric substrates. This method avoids the use of NaOH, however, poor adhesion of the particles to the substrates were noted on porous substrates and no significant pyrophoric response was generated on the spin-coated, non-porous substrates. It is believed that this lack of response is due to the amount of material coated on the surface of the steel substrate and the high thermal conductivity of the steel substrate causing the quenching of the oxidation reaction from heat loss.
Thus a need exists for safer, environmentally benign, and more efficient methods for preparing pyrophopric materials that provides the same performance standards as current iron coated on steel pyrophopric decoys.
Disclosed herein are composite materials for use in countermeasure decoys. In one embodiment, the composite material comprises nanoporous pyrophoric alpha iron nanoparticles dispersed in a ceramic matrix, wherein the ratio of the iron to ceramic is 41:59 to 93:7.
In one feature of this embodiment, the composite material comprises a fuel.
In yet another feature of this embodiment, the ceramic material is porous and has a porosity of between 10% to 40%.
In another embodiment, the composite material is shaped into strips and packaged into canisters for use as an aerial countermeasure decoy.
In yet another embodiment, a process is disclosed for preparing the composite material. The process comprises mixing alpha iron oxide nanoparticles, a ceramic material, and an optional binder with a liquid to create a free-flowing slurry. The slurry is tape casted into a thin flat film and dried. The thin flat film is further sintered and reduced under hydrogen gas to activate the alpha iron nanoparticles into pyrophoric alpha iron nanoparticles.
The invention will be better understood, and further objects, features and advantages thereof will become more apparent from the following description of the preferred embodiments, taken in conjunction with the accompanying drawings.
The present invention discloses a pyrophoric composite material useful as countermeasure decoys and methods for preparing the same. The methods provided herein eliminates the need for using caustic chemicals for preparing nanoporous pyrophoric alpha iron nanoparticles. The disclosed method has the added benefit of a self-supporting matrix, thereby eliminating the need for a substrate. The process utilizes resonant acoustic mixing to disperse alpha iron oxide nanoparticles and ceramic into a mixture. The mixture is then tape casted into a desired thickness. The alpha iron oxide dispersed in the ceramic is then reduced to convert alpha iron oxide into porous pyrophoric alpha iron nanoparticles. The pyrophoric response of the iron can be adjusted (i.e. tuned) based on the iron/ceramic material weight ratio and/or the addition of other fuels such as Mg, Al etc.
As used herein, the term pyrophoric means the ability to self-ignite spontaneously upon exposure to air.
The general processing steps for preparing the nanoporous pyrophoric alpha iron nanoparticles and ceramic composite material is as follows:
The composite material prepared by the process described herein comprises nanoporous pyrophoric alpha iron nanoparticles wherein the alpha iron spontaneously self-ignites upon exposure to air. The nanoporous pyrophoric alpha iron nanoparticles are dispersed in an interconnected matrix of porous ceramic material. It should be understood that the ceramic material should be sufficiently porous to permit oxygen in the atmosphere to permeate and react with the pyrophoric alpha iron disperse through the entire structure such that spontaneous self-ignition of the iron is achieve at under 2 seconds, with output temperatures reaching as high as about 600° C. to about 800° C. as illustrated in
Composite Mix.
Alpha iron oxide nanoparticles and ceramic material, at ratio of 50:50 to 90:10 by weight, may be dispersed with liquid into a free flowing slurry. The materials may be uniformly mixed using any known methods that produces a homogenous mixture. Resonant acoustic mixer (RAM) is preferred. Such mixers are available from Resodyn Acoustic®. Nanoparticles of alpha iron oxide having a size no greater than 100 nm and preferably between 20 nm-60 nm may be used. The liquid may be water or an organic solvent, however, any liquid that promotes flowability of the slurry during the tape casting process may be utilized. A preferred liquid is water. Ceramic material such as aluminum silicate may be mixed with the alpha iron oxide nanoparticle, however, sodium silicate, lithium silicate, magnesium silicate, bentonite, montmorillonite, Boehmite, and feldspar may be used as well. Polymeric binders may optionally be added to the mixture. Such binders include methylcellulose, hydroxypropyl methylcellulose, and ethylcellulose as well as other high viscosity binders soluble in the selected solvent may be used. Fuel components may optionally be added to modify the dynamic combustion of the self-supporting pyrophoric material. Such fuel additives include aluminum, silicon, tin and magnesium with tin being preferred.
Tape casting. After the composite slurry is prepared, it may be tape casted using an apparatus having the general features illustrated in
Sintering.
The composite tape is further processed by partial sintering to remove the binder, initiate inter-particle connections, and reduce the porosity which all leads to increased strength. Sintering of the composite is conducted at temperatures between 980° C. to 1200° C. with soak times between 10 minutes and 5 hours in air or under an inert atmosphere. The temperature and soak times may be varied, in accordance with generally known methods.
Iron Reduction.
The alpha iron oxide in the composite material is reduce to nanoporous pyrophoric alpha iron nanoparticles using hydrogen to produce water as a byproduct in this step. Reduction of alpha iron occurs under a flowing hydrogen environment, preferably at temperatures of 400° C. to 550° C. for a minimum of 3 hours. The reduced composite is then cooled under a flowing hydrogen, nitrogen or a mixed hydrogen/nitrogen atmosphere.
Packaging.
The iron and ceramic composite tape or film may be further processed into strips and packaged as a plurality of geometric shaped strips under a dry inert atmosphere (hydrogen and/or nitrogen) into canisters that can be ejected from an aircraft. Typical geometric shape strips include 1″×1″ squares packaged into a canister having inner dimensions of 1″×1″×8″.
Example 1 is an illustration of the disclosed invention. Weighing out of the following components: i) alpha iron oxide (27 grams), ii) aluminum silicate (3 grams) iii) methylcellulose (1.5 grams) and iv) water (67.5 mL). In certain cases, additional fuels such as Al, Mg, Ti etc. may be added to the mixture. Disperse the methylcellulose powder in the water and allow for complete hydration of the methylcellulose over a 16-hour period. Add the alpha iron oxide and aluminum silicate to the mixing container containing the methylcellulose solution and disperse using an acoustic mixing technique. The composite slurry is then tape casted onto a Teflon or other suitable non-sticking plate or film using a doctor blade. The composite tape is allowed to dry for 12 hours under ambient conditions. The composite tape is then cut into pieces (size dependent on end application). The substrates are sintered in air at 10-15° C. above the silicate melting point with a soak time of 10 minutes to 3 hours. Hydrogen reduction of the alpha iron oxide is conducted, followed by testing or packaging.
In another example, 80% alpha iron oxide nanoparticles and 20% sodium silicate by weight were dispersed in water. The mixture was tape casted as described in the procedures above and sintered at 1100° C. for 30 minutes and further reduced under flowing hydrogen.
Although the subject invention has been described above in relation to embodiments thereof, it will be understood by those skilled in the art that variations and modifications can be effected in these preferred embodiments without departing from the scope and spirit of the invention.
The present application is a non-provisional application that claims the benefit of provisional application entitled “Ceramic Bonded Pyrophoric Substrates” filed on Apr. 21, 2015 as Ser. No. 62/150,458 the disclosure of which is incorporated in its entirety herein.
The inventions described herein may be manufactured and used by or for the United States Government for government purposes without payment of any royalties.
| Number | Name | Date | Kind |
|---|---|---|---|
| 4895609 | Baldi | Jan 1990 | A |
| 8623156 | Haines | Jan 2014 | B1 |
| 20060042417 | Gash | Mar 2006 | A1 |
| Number | Date | Country | |
|---|---|---|---|
| 62150458 | Apr 2015 | US |
