The invention relates in general to heat generating structures, and more particularly to a relatively slow burning, gasless heating element that may be utilized for various purposes such as a delay element or fuse that ignites an explosive device or material.
It is known that a heat generating structure composed of two dissimilar materials such as metals may be used as an ignitable delay element or fuse. The delay element may be used in varied applications to safely initiate the timed ignition or detonation of an explosive device or material. These heat generating structures can come in many different physical forms. For example, known ignitable delay elements comprised of compressed powder mixtures can be unreliable and exhibit unacceptable delay timing (e.g., timing differences between similarly manufactured elements) or initiation-sensitive variations. These problems are due, for example, to particle size distribution inconsistencies, inadequate mixing, free volume and pressure. In addition, such an undesirable performance variation tends to become more pronounced as the propagation rate of the delay element is reduced. Further, powder-type delay mixtures produce at least some gas, the production of which requires the incorporation of hardware structures that prevent the premature and undesired heating and possible ignition of the “target” (the substance, often an explosive, which ignites when the delay has run its course or completed its propagation) by such hot gas production. Also, the production of such gases by these powder mixtures is oftentimes influenced by pressure and packing variations.
Other known heat generating structures that can be used as delay elements include that which is commercially available under the brand name Pyrofuze® provided by the Sigmund Cohn Corporation of Mount Vernon, N.Y. This device comes in wire or ribbon form and comprises two metallic elements in intimate contact with one another: an inner core of aluminum surrounded by an outer jacket of palladium. When the two metallic elements are brought to the initiating temperature by a sufficient amount of heat, the metals react by alloying rapidly resulting in instant deflagration without support of oxygen. Once the alloying reaction is started, the reaction will not stop until alloying is completed. One drawback with the Pyrofuze® delay element is that it typically burns at a relatively rapid rate.
Another commercially available heat generating structure that can be used as a delay element or fuse is provided under the brand name NanoFoil® by Reactive NanoTechnologies, Inc. of Hunt Valley, Md. The NanoFoil® device is a multilayer foil comprised of thousands of alternating nanoscale thin layers of aluminum and nickel. When initiated by an electrical, thermal, mechanical or optical source, the metals will mix or alloy and react to release heat energy. However, when used as a delay element or fuse, the NanoFoil® multilayer foil tends to have a burn rate that is relatively fast, and the burn rate is not easily variable. The NanoFoil® multilayer foil is also relatively expensive.
What is needed is a relatively slow burning, gasless, heat generating structure composed of two or more dissimilar materials, such as metals, distributed in a non-uniform three-dimensional manner along its propagation or burn path, where the structure when ignited exhibits an exothermic alloying reaction between the materials and can function as a delay element or fuse in providing for reliable propagation and, thus, accurate ignition of an explosive device.
According to an aspect of the invention, a heat generating structure includes a substrate comprised of a first material and a second material coating at least a portion and preferably all of the first material, where the second material is different from the first material, where the materials, upon being thermally energized, react with each other in an exothermic and self-sustaining alloying reaction that propagates from a first location within the structure along a travel path to a second location within the structure at a rate that depends upon one or more characteristics of the first and second materials.
The present invention is predicated on that fact that the exothermic reaction between the dissimilar materials comprising the heat generating structure can be made to occur at a relatively slower propagation or burn rate than prior art devices in part not only due to the composition of the dissimilar materials selected but also due to the three-dimensional characteristics of the substrate portion of the structure; in particular, to a non-uniform and varying distribution of the mass of the substrate and corresponding coating along the direction of the propagation or burn path. These three-dimensional characteristics result in the transmission of heat into a structure comprising a substrate with a network of many different burn or propagation directions at one or more instants in time, in addition to the propagation direction along the desired burn path. As described in detail hereinafter, such a substrate with a network of many different propagation directions can be achieved, for example, by a mesh or foam structure.
These and other objects, features and advantages of the present invention will become more apparent in light of the following detailed description of preferred embodiments thereof, as illustrated in the accompanying drawings.
Referring to
Referring to
In a preferred embodiment, the coating 22 comprises nickel that is applied onto the outer surface of each of the wires 20 of the aluminum metal mesh substrate 18 by, for example, electroplating or other methods such as vacuum sputtering or through an electroless process. The nickel coating 22 may include other materials including boron, phosphorus and/or palladium. Also, if aluminum is utilized as the mesh substrate material, any aluminum oxide that is present on the outer surface of the aluminum wires 20 may be removed and a coating of zinc may be applied to the outer surface of the wires 20. The zinc may allow initiation or ignition of the structure 16 at a lower temperature than if the zinc were not present. In the alternative, the zinc coating may be removed if an electroless process is used to coat the nickel onto the aluminum wire 20. The amount of nickel that is coated onto the aluminum mesh wires 20 may be in a one to one ratio with the underlying aluminum wires 20; that is, the nickel may be in an equivalent molar content as that of the aluminum. The heat generating structure 16 may be considered to be a reactive multilayer laminate comprising the substrate 18 and the coating 22, with both the substrate 18 and the coating 22 comprising reactive metals in a preferred embodiment.
The materials (e.g., metals) comprising the substrate 18 and the coating 22 are selected based on their individual characteristics, such as melting point and density, and in combination for enthalpy of alloying. For any bimetallic structure comprising a substrate of a first metal coated with a second, different metal to propagate, the formation of alloys from the individual metal constituent components must be exothermic. This heat evolved warms not only the surrounding environment, but also the continuous metal structure. After a source of ignition (e.g., a match or heating element) is applied to the structure 16 of the present invention, the alloying temperature of at least one of the metals (typically that of the aluminum wire 20 first) is eventually achieved and the materials are thermally energized and react with each other such that further alloying between the two metals is induced. Accordingly, heat is liberated with resulting propagation in a self-sustaining manner throughout the entire continuous heat generating structure 16 from a first or starting point within the structure and along a travel path to a second or ending or discharge point within the structure, and preferably in a controlled and repeatably manufacturable manner. The starting and ending points are typically spaced from each other with the travel path in between.
For example, if the structure is of a three-dimensional, rectangular-shape, once ignited at a first or starting end of the structure 16, the thermal energization of the reactive materials comprising the structure will cause the propagation to continue through to the second or discharge end at a consistent timed rate depending on the intermetallic or bimetallic (or non-metallic) composition of the structure 16 as well as on the geometric configuration (e.g., thickness of wires 20, wire crossing frequency) of the structure 16. Located at the second end of the structure 16 is some type of explosive device or material (e.g., fireworks, blasting caps, etc.) that is ignited when the propagation reaches this second end of the structure. Thus, by controlling the composition and the configuration of the reactive materials comprising the heat generating structure 16, the burn or propagation rate can be controlled (that is, the reaction rate or time period for propagation from the first end to the second end along the travel path of the reactive material can be selected).
More specifically, the exothermic reaction between the dissimilar materials comprising the heat generating structure 16 can be made to occur at a relatively slower propagation or burn rate than prior art devices in part not only due to the composition of the dissimilar materials selected but also due to the three-dimensional characteristics of the substrate portion 18 of the structure; in particular, to a non-uniform and varying distribution of the mass of the substrate and corresponding coating along the direction of the primary propagation or burn path. For example, if the mesh structure 16 of
Referring to
The three-dimensional characteristics of the heat generating structure of the present invention result in the transmission of heat into a structure comprising a substrate with a network of many different burn or propagation directions at one or more instants in time, in addition to the propagation direction along the desired burn path. This is particularly true with respect to the foam substrate 30 as compared to the mesh substrate 18 in terms of the number of different burn or propagation directions at one or more instants in time. Unlike systems based on compacted powder, the continuous nature of the mesh substrate 18 or foam substrate 30 and the intimate contact between the metal coating the substrates eliminates the pressure dependency required for intimate contact between layers. Thus, the burn rate of the structure is less dependent upon pressure. Failures are also reduced as a consequence of the many filaments and intersections inherent in the substrates 18, 30. In addition, consistency is enhanced since the exothermicity is controlled by the content of the metals, which content is, in turn, characterized by easily measurable and controllable weights and thicknesses (i.e., a composition and a configuration).
In general, any material that can be prepared or formed as a foam substrate 30, a mesh substrate 18, or other non-completely-solid substrate may be used as the substrate. This includes various metals and non-metals. In a preferred embodiment, the substrate material comprises aluminum and the coating comprises nickel coated that is either pure or combined with boron and/or phosphorus. The material comprising the substrate is typically selected in accordance with or in dependence on the material that will be coated onto the substrate. The material coated onto the substrate is preferably deposited in a reliable and consistent manner, for example by electrochemical means such as electroplating or by an autoctalytic electroless process. The materials that may comprise the substrate wires and/or the wire coating may include those from the group of reactive metals including aluminum, boron, carbon, silicon, zirconium, iron, copper, beryllium, tungsten, hafnium, antimony, magnesium, molybdenum, zinc, tin, nickel, palladium, phosphorus, sulfur, tantalum, manganese, cobalt, chromium, and vanadium.
Also, metal particles such as aluminum, magnesium, boron, beryllium, zirconium, titanium, zinc may be used in combination with fluoropolymers such as polytetrafluoroethylene, fluoroelastomers, fluorosurfactants, or fluoroadditives. As such, the metals may be formed in finely divided particles within a matrix of one of the polymers and extruded to form a wire-like structure such as a filament which is then integrated into the structure of the substrate (e.g., the wire mesh substrate 18 of
Further, the following non-energetic polymers can be combined with any of the above materials to form the substrate: hydroxy terminated polybutadiene, hydroxy terminated polyether, carboxy terminated polybutadiene, polyether, polycaprolactone, or polyvinyl chloride. Alternatively, such a combination of non-energetic polymers can be placed inside of an aluminum tube, where a plurality of such tubes comprise the substrate. In addition, there exist many powder-based reactions composed of a fuel and an oxidizer that constitute the bulk of pyrotechnic formulations. Incorporating these into the heat generating structure of the present invention necessitates the use of a binder material, such as the energetic polymers and plasticizers listed above or the non-energetic polymers listed above, together with a non-reacting metal wire material.
Referring to
Referring to
Although the present invention has been illustrated and described with respect to several preferred embodiments thereof, various changes, omissions and additions to the form and detail thereof, may be made therein, without departing from the spirit and scope of the invention.
This invention was made with Government support under contract W909MY-06-C-0041 awarded by the U.S. Army. The Government has certain rights in this invention.
Number | Name | Date | Kind |
---|---|---|---|
3086894 | Baggett et al. | Apr 1963 | A |
3111396 | Ball | Nov 1963 | A |
3319520 | Stefano et al. | May 1967 | A |
3430564 | Silvia et al. | Mar 1969 | A |
3503814 | Helms et al. | Mar 1970 | A |
3509822 | Rice et al. | May 1970 | A |
3730093 | Cummings | May 1973 | A |
3768409 | Menz et al. | Oct 1973 | A |
4053337 | Collins | Oct 1977 | A |
4349612 | Baldi | Sep 1982 | A |
4429632 | Yunan | Feb 1984 | A |
4696231 | Bryan | Sep 1987 | A |
4815386 | Dillard et al. | Mar 1989 | A |
5031538 | Dufrane et al. | Jul 1991 | A |
5046425 | Gibbons et al. | Sep 1991 | A |
5182417 | Rontey et al. | Jan 1993 | A |
5495819 | Marion | Mar 1996 | A |
5547715 | Barbee et al. | Aug 1996 | A |
5843538 | Ehrsam et al. | Dec 1998 | A |
6006671 | Yunan | Dec 1999 | A |
6010610 | Yih | Jan 2000 | A |
6170398 | Rabotinsky et al. | Jan 2001 | B1 |
6863992 | Weihs et al. | Mar 2005 | B2 |
6886327 | Nathal et al. | May 2005 | B1 |
7383775 | Mock et al. | Jun 2008 | B1 |
20050067072 | Vavrick | Mar 2005 | A1 |
20050142404 | Boucher et al. | Jun 2005 | A1 |
Number | Date | Country |
---|---|---|
102006001838 | Jul 2007 | DE |
2224729 | May 1990 | GB |
9424074 | Oct 1994 | WO |
WO 2004106268 | Dec 2004 | WO |
2006086274 | Aug 2006 | WO |
WO 2007095303 | Aug 2007 | WO |
Number | Date | Country | |
---|---|---|---|
20090031911 A1 | Feb 2009 | US |