US20130199397A1 - Multi component reactive metal penetrators, and their method of manufacture - Google Patents
Multi component reactive metal penetrators, and their method of manufacture Download PDFInfo
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- US20130199397A1 US20130199397A1 US11/764,106 US76410607A US2013199397A1 US 20130199397 A1 US20130199397 A1 US 20130199397A1 US 76410607 A US76410607 A US 76410607A US 2013199397 A1 US2013199397 A1 US 2013199397A1
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- 239000000843 powder Substances 0.000 claims description 7
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- 229910052684 Cerium Inorganic materials 0.000 claims description 3
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- 229910052777 Praseodymium Inorganic materials 0.000 claims description 3
- 229910052772 Samarium Inorganic materials 0.000 claims description 3
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Images
Classifications
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F42—AMMUNITION; BLASTING
- F42B—EXPLOSIVE CHARGES, e.g. FOR BLASTING, FIREWORKS, AMMUNITION
- F42B12/00—Projectiles, missiles or mines characterised by the warhead, the intended effect, or the material
- F42B12/72—Projectiles, missiles or mines characterised by the warhead, the intended effect, or the material characterised by the material
- F42B12/74—Projectiles, missiles or mines characterised by the warhead, the intended effect, or the material characterised by the material of the core or solid body
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
- B22D23/00—Casting processes not provided for in groups B22D1/00 - B22D21/00
- B22D23/06—Melting-down metal, e.g. metal particles, in the mould
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F42—AMMUNITION; BLASTING
- F42B—EXPLOSIVE CHARGES, e.g. FOR BLASTING, FIREWORKS, AMMUNITION
- F42B12/00—Projectiles, missiles or mines characterised by the warhead, the intended effect, or the material
- F42B12/02—Projectiles, missiles or mines characterised by the warhead, the intended effect, or the material characterised by the warhead or the intended effect
- F42B12/04—Projectiles, missiles or mines characterised by the warhead, the intended effect, or the material characterised by the warhead or the intended effect of armour-piercing type
- F42B12/06—Projectiles, missiles or mines characterised by the warhead, the intended effect, or the material characterised by the warhead or the intended effect of armour-piercing type with hard or heavy core; Kinetic energy penetrators
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/02—Compacting only
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/10—Sintering only
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/12—Both compacting and sintering
- B22F3/14—Both compacting and sintering simultaneously
- B22F3/15—Hot isostatic pressing
Definitions
- the present invention relates to penetrators and methods for their manufacture.
- Penetrators are used as a weapon against airborne or land based targets. These penetrators can take the form of a metal cube, (e.g. 1 ⁇ 4′′ ⁇ 1 ⁇ 4′′ ⁇ 1 ⁇ 4′′), or an explosively formed penetrator with a 3-dimensional geometry. When explosively launched they can cause significant damage by penetrating the outer surface or skin of a target such as an aircraft, missile, tank or other vehicle owing to their momentum. As such, it is preferable to make these penetrator cubes from a heavy metal. Historically, steel (7.85 gm/cc) has been used for these penetrators.
- a second type of penetrator depends on reactive energy release. After penetrating the skin of the target, a fragment of reactive material can react with oxygen to create a sustainable reaction. The latter produces both a fire start capability and overpressure within the target volume.
- Materials with sufficient reactivity include zirconium (6.3 g/cc), aluminum (2.7 g/cc), or magnesium (1.74 g/cc). However, the relatively low density of these materials makes them less suitable as kinetic energy penetrators.
- LaRocca in U.S. Pat. No. 4,807,795 describes a method for producing a bimetallic conoid. The method consists of first explosively bonding two metal disks and then shear-forming the bonded disks into a conoidal shape simultaneously over a mandrel.
- McCubbin in U.S. Pat. No. 5,567,908 describes a reactive case warhead comprised of magnesium, aluminum, zinc and zirconium that is made in such a manner as to maximize blast damage once the warhead penetrates the external shell of a target.
- the warhead employs a hardened steel front plate made in such a way to penetrate the walls of the target and that is specially shaped to insure a ripping or tearing of the exterior walls as the warhead enters.
- An end-loaded fuse ignites the explosive charge and reactive case at the proper time.
- bimetallic penetrator is a shaped penetrator which has a 3-dimensional geometry and is produced by the explosive forming process.
- the presence of possible non-uniformities resulting from the layered bimetallic structure also could cause difficulties in the explosive forming process.
- the present invention overcomes the aforesaid and other disadvantages of the prior art.
- a penetrator formed of an alloy or composite of a high density metal and a reactive material Unlike the bimetallic structures of the prior art, a penetrator made of a composite or an alloy has a uniform structure throughout.
- a penetrator formed, for example, of a high density metal and a reactive metal will have sufficient mass to penetrate steel plate, and upon striking the steel plate, provide a very substantial release of energy which would be seen to compare favorably to that obtained with a penetrator formed only of a high density metal or a penetrator formed only of a reactive metal, of the same size, launched at the same speed.
- FIG. 1 is an optical image of a prior art steel penetrator gun launch at 5,370 feet/second showing impact with the back wall of a test chamber;
- FIG. 2 is an optical image of a prior art tantalum (Ta) penetrator gun launch at 5,818 feet/second showing impact with the back wall of a test chamber;
- Ta tantalum
- FIG. 3 is an optical image of a prior art zirconium (Zr) penetrator gun launch at 5,797 feet/second showing impact with the back wall of a test chamber;
- FIG. 4 is a schematic view showing production of a Ta/Zr alloy penetrator in accordance with the present invention.
- FIG. 5 is an optical image of a Ta/Zr alloy penetrator gun launch at 7,242 feet/second showing impact with the back wall of a test chamber;
- FIG. 6 is an optical image of a Ta/Zr layered composite penetrator gun launch at 6,255 feet/second showing impact with the back wall of a test chamber.
- the present invention provides penetrators formed of a composite or an alloy of a high density metal and a reactive material.
- high density metal means a metal having a density of greater than about 13.1 g/cc or about 817 lbs./cu feet.
- reaction material means a material that is capable of substantial energy release, e.g., through oxidation reaction.
- the homogeneity of the a composite or alloy provides an extremely uniform structure which will facilitate the manufacture of shaped penetrators by the explosive forming process. Comparable uniformity and energy release can be obtained by utilizing a particulate composite manufactured using a powder of one metal and a molten metal of a second composition, e.g. Ta metal in a Zr matrix.
- a particulate composite manufactured using a powder of one metal and a molten metal of a second composition e.g. Ta metal in a Zr matrix.
- Other heavy and/or reactive metals can be used in the manufacture of alloy and particulate composites in accordance with the present invention, e.g. an alloy of W as the heavy metal with Zr as the reactive metal. More than two metals can be used as well, e.g. ternary, quaternary and higher composition alloys and particulate composites.
- the alloys and particulate composites can be manufactured by any process that melts one or more of the metals. This can include, but is not limited to, the use of a plasma torch such as a welding torch, laser, furnace melting, arc melting, and induction and e-beam melting. Alternatively hot consolidation can be employed such as hot pressing in a die, hot isostatic pressing (HIP), and cold pressing followed by sintering below or above the melting point of one of the constituents such as the active metal zirconium.
- a plasma torch such as a welding torch, laser, furnace melting, arc melting, and induction and e-beam melting.
- hot consolidation can be employed such as hot pressing in a die, hot isostatic pressing (HIP), and cold pressing followed by sintering below or above the melting point of one of the constituents such as the active metal zirconium.
- a Zr penetrator can penetrate the target structure, a very high level of reaction is obtained, which is desirable for weapon lethality.
- the pressure buildup in the chamber, and the extent of reaction as indicated by residue after testing indicates the alloy composition is more effective than a pure Zr layer. It is believed that the increased pressure is the result of increased surface area in the alloy fragment after impact with the target when compared to the response of a pure Zr or the layered bimetallic penetration.
- a penetrator formed of Ta/Zr alloy would have a considerably higher mass density which would result in greater penetration capability than Zr alone.
- Preferred as high density metals in accordance with the present invention are Ta, W, Re, Os, Ir, Pt, Au, U, and Hf, and an alloy thereof.
- Preferred as reactive materials in accordance with the present invention are reactive metals such as Zr, Mg, Al, Li, Be, Ti, Sc, V, H, Sr, Y, Si, Ge, and Nd, and an alloy thereof, or a rare earth metal and an alloy thereof, e.g., La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, En, Tm, Yb and Lu.
- Other reactive materials include hydrogen or carbon or a metal carbide.
- a Ta cube with dimensions of 1 ⁇ 4′′ was gun launched at a speed of 5818 ft/sec and targeted at a steel encased test chamber.
- the experiment was instrumented with pressure transducers attached to the target chamber, an optical pyrometer to measure temperature, and a high speed digital camera to image the energy release.
- the cube penetrated the 0.060′′ mild steel entrance plate, and then traversed the target chamber to a 3 ⁇ 4′′ rear plate.
- the energy release as noted by optical imaging is shown in FIG. 2 and appears higher than that observed for the steel cube in Example 1.
- a pressure increase to 2.1 psi was recorded. This is a result of Ta having a greater reactivity with oxygen than steel.
- the maximum temperature in the chamber was ⁇ 1500° K. This is the lowest temperature that can be measured. It was estimated that >30% of the original penetrator mass remained on the chamber floor after the test was completed.
- a Zr cube with dimensions of 1 ⁇ 4′′ was gun launched at a speed of 5297 ft/sec and targeted at a steel encased test chamber.
- the experiment was instrumented with pressure transducers attached to the target chamber, an optical pyrometer to measure temperature, and a high speed digital camera to image the energy release.
- the cube penetrated the 0.060′′ mild steel entrance plate, and then traversed the target chamber to a 3 ⁇ 4′′ rear plate.
- the energy release as noted by optical imaging is shown in FIG. 3 and appears much higher than that observed for the steel cube in Example 1 or the Ta cube shown in Example 2.
- a pressure increase to 7.3 psi and a temperature increase to 4500° K were recorded.
- An alloy of Ta and Zr was prepared by melting Zr and Ta metals in the arc of a plasma transferred arc (PTA) welding torch and depositing the product in a graphite crucible as shown in FIG. 4 .
- a current of 250 amps was used for the PTA torch, which was sufficient to melt both the Ta powder and Zr wire.
- the molar ratio was approximately 1.3Ta:1Zr.
- the alloy was machined into cubes with dimensions of 1 ⁇ 4′′ by EDM machining. The cubes were gun launched at a speed of 7242 ft/sec and targeted at a steel encased test chamber.
- the experiment was instrumented with pressure transducers attached to the target chamber, an optical pyrometer to measure temperature, and a high speed digital camera to image the energy release.
- the cube penetrated the 0.060′′ mild steel entrance plate, and then traversed the target chamber to a 3 ⁇ 4′′ rear plate.
- the energy release as noted by optical imaging is shown in FIG. 5 , and appears comparable to that obtained for pure Zr in Example 3.
- a temperature rise to 4800° K was measured in the chamber with a pressure of 12.5 psi. It was estimated that ⁇ 5% of the original penetrator mass remained on the chamber floor after the test was completed, indicating a very high level of reaction.
- a layered composite of Ta and Zr was prepared by depositing a layer of Zr on each side of a 1 ⁇ 8′′ Ta plate at a torch amperage of 225 amps. After cooling to room temperature, the alloy was machined into cubes with a dimension of 1 ⁇ 4′′ by EDM machining. The molar ratio of the Ta and the Zr in the cubes was approximately 1.3Ta:1Zr. The cubes were gun launched at a speed of 6255 ft/sec and targeted at a steel encased test chamber. The experiment was instrumented with pressure transducers attached to the target chamber, an optical pyrometer to measure temperature, and a high speed digital camera to image the energy release.
- the energy release as noted by optical imaging is shown in FIG. 5 .
- An alloy of W and Zr was prepared using the experimental setup as shown in FIG. 4 with a feed of W powder and Zr wire. An amperage for the PTA torch of 280 amps was used which was sufficient to melt both metals. After cooling to room temperature, the alloy was machined into cubes with a dimension of 1 ⁇ 4′′ by EDM machining. The molar ratio of the W and the Zr in the cubes was approximately 1.3W:1Zr. The cubes were gun launched tested by targeting the penetrator cube at a steel encased test chamber which was instrumented with optical imaging.
- a particulate composite of Ta and Zr was prepared using the experimental setup as shown in FIG. 4 using a feed of Ta powder and Zr wire and with an amperage for the PTA torch of 190 amps. This power level was sufficient to melt the Zr metal but not the Ta powder. After cooling to room temperature, the composite was machined into cubes with a dimension of 1 ⁇ 4′′ by EDM machining. The molar ratio of the Ta and the Zr in the cubes was approximately 1.3Ta:1Zr. The cubes were gun launched and targeted at a steel encased test chamber which was instrumented with optical imaging.
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- Chemical & Material Sciences (AREA)
- Combustion & Propulsion (AREA)
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Abstract
A penetrator comprising a layered composite of at least one high density metal and at least one reactive material such as a reactive metal.
Description
- This application is a divisional of U.S. patent application Ser. No. 11/764,036, filed Jun. 15, 2007, and claims priority from U.S. Provisional Application Ser. No. 60/805,124, and U.S. Provisional Application Ser. No. 60/805,128, both filed Jun. 19, 2006, the contents of which are incorporated hereby reference.
- This invention was made in part with Government support under contract number FA8651-05-C-0103 awarded by the U.S. Air Force. The Government may have certain rights in the invention.
- The present invention relates to penetrators and methods for their manufacture.
- Penetrators are used as a weapon against airborne or land based targets. These penetrators can take the form of a metal cube, (e.g. ¼″×¼″×¼″), or an explosively formed penetrator with a 3-dimensional geometry. When explosively launched they can cause significant damage by penetrating the outer surface or skin of a target such as an aircraft, missile, tank or other vehicle owing to their momentum. As such, it is preferable to make these penetrator cubes from a heavy metal. Historically, steel (7.85 gm/cc) has been used for these penetrators. However, heavier metals such as tantalum (Ta—16.3 g/cc) or depleted uranium (U—18.9 g/cc) are also of interest. The momentum of the high density projectile gives it outstanding properties as a penetrator.
- A second type of penetrator depends on reactive energy release. After penetrating the skin of the target, a fragment of reactive material can react with oxygen to create a sustainable reaction. The latter produces both a fire start capability and overpressure within the target volume. Materials with sufficient reactivity include zirconium (6.3 g/cc), aluminum (2.7 g/cc), or magnesium (1.74 g/cc). However, the relatively low density of these materials makes them less suitable as kinetic energy penetrators.
- Thus, there is a need for penetrators which combine both high density for purposes of penetration, as well as reactivity.
- LaRocca in U.S. Pat. No. 4,807,795 describes a method for producing a bimetallic conoid. The method consists of first explosively bonding two metal disks and then shear-forming the bonded disks into a conoidal shape simultaneously over a mandrel. McCubbin in U.S. Pat. No. 5,567,908 describes a reactive case warhead comprised of magnesium, aluminum, zinc and zirconium that is made in such a manner as to maximize blast damage once the warhead penetrates the external shell of a target. The warhead employs a hardened steel front plate made in such a way to penetrate the walls of the target and that is specially shaped to insure a ripping or tearing of the exterior walls as the warhead enters. An end-loaded fuse ignites the explosive charge and reactive case at the proper time. Both of these prior patented inventions have inherent limitations, and are difficult to manufacture.
- In our earlier. U.S. Provisional Application Ser. No. 60/729,533, filed Oct. 20, 2005, we describe a bimetallic layered penetrator of Zr/Ta/Zr produced by the plasma transferred arc solid free form fabrication (PTA SFFF) process. The resulting bimetallic layered penetrator was found to have sufficient mass and momentum to penetrate a target, and carry the reactive Zr into the target, resulting in considerably more damage than a non-reactive penetrator such as steel, and was particularly suited for manufacture of cube geometry penetrators. However, the presence of non-uniformities resulting from the layered bimetallic structure can cause difficulties in the explosive launch process.
- Another type of bimetallic penetrator is a shaped penetrator which has a 3-dimensional geometry and is produced by the explosive forming process. However, the presence of possible non-uniformities resulting from the layered bimetallic structure also could cause difficulties in the explosive forming process.
- The present invention overcomes the aforesaid and other disadvantages of the prior art. In accordance with the present invention we provide a penetrator formed of an alloy or composite of a high density metal and a reactive material; Unlike the bimetallic structures of the prior art, a penetrator made of a composite or an alloy has a uniform structure throughout. Thus, a penetrator formed, for example, of a high density metal and a reactive metal will have sufficient mass to penetrate steel plate, and upon striking the steel plate, provide a very substantial release of energy which would be seen to compare favorably to that obtained with a penetrator formed only of a high density metal or a penetrator formed only of a reactive metal, of the same size, launched at the same speed.
- Further features and advantages of the present invention will be seen from the following detailed description, taken in conjunction with the accompanying drawings, wherein like numerals depict like parts, and wherein:
-
FIG. 1 is an optical image of a prior art steel penetrator gun launch at 5,370 feet/second showing impact with the back wall of a test chamber; -
FIG. 2 is an optical image of a prior art tantalum (Ta) penetrator gun launch at 5,818 feet/second showing impact with the back wall of a test chamber; -
FIG. 3 is an optical image of a prior art zirconium (Zr) penetrator gun launch at 5,797 feet/second showing impact with the back wall of a test chamber; -
FIG. 4 is a schematic view showing production of a Ta/Zr alloy penetrator in accordance with the present invention; -
FIG. 5 is an optical image of a Ta/Zr alloy penetrator gun launch at 7,242 feet/second showing impact with the back wall of a test chamber; and -
FIG. 6 is an optical image of a Ta/Zr layered composite penetrator gun launch at 6,255 feet/second showing impact with the back wall of a test chamber. - The present invention provides penetrators formed of a composite or an alloy of a high density metal and a reactive material.
- As used herein the term “high density metal” means a metal having a density of greater than about 13.1 g/cc or about 817 lbs./cu feet. The term “reaction material” means a material that is capable of substantial energy release, e.g., through oxidation reaction.
- The homogeneity of the a composite or alloy provides an extremely uniform structure which will facilitate the manufacture of shaped penetrators by the explosive forming process. Comparable uniformity and energy release can be obtained by utilizing a particulate composite manufactured using a powder of one metal and a molten metal of a second composition, e.g. Ta metal in a Zr matrix. Other heavy and/or reactive metals can be used in the manufacture of alloy and particulate composites in accordance with the present invention, e.g. an alloy of W as the heavy metal with Zr as the reactive metal. More than two metals can be used as well, e.g. ternary, quaternary and higher composition alloys and particulate composites. The alloys and particulate composites can be manufactured by any process that melts one or more of the metals. This can include, but is not limited to, the use of a plasma torch such as a welding torch, laser, furnace melting, arc melting, and induction and e-beam melting. Alternatively hot consolidation can be employed such as hot pressing in a die, hot isostatic pressing (HIP), and cold pressing followed by sintering below or above the melting point of one of the constituents such as the active metal zirconium.
- As can be seen in the examples below if a Zr penetrator can penetrate the target structure, a very high level of reaction is obtained, which is desirable for weapon lethality. With a Ta/Zr alloy, the pressure buildup in the chamber, and the extent of reaction as indicated by residue after testing indicates the alloy composition is more effective than a pure Zr layer. It is believed that the increased pressure is the result of increased surface area in the alloy fragment after impact with the target when compared to the response of a pure Zr or the layered bimetallic penetration. Compared to pure Zr, a penetrator formed of Ta/Zr alloy would have a considerably higher mass density which would result in greater penetration capability than Zr alone.
- Preferred as high density metals in accordance with the present invention are Ta, W, Re, Os, Ir, Pt, Au, U, and Hf, and an alloy thereof. Preferred as reactive materials in accordance with the present invention are reactive metals such as Zr, Mg, Al, Li, Be, Ti, Sc, V, H, Sr, Y, Si, Ge, and Nd, and an alloy thereof, or a rare earth metal and an alloy thereof, e.g., La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, En, Tm, Yb and Lu. Other reactive materials include hydrogen or carbon or a metal carbide.
- The invention will be further demonstrated by the following non-limiting examples:
- In this test, a steel cube with dimensions of ¼″ was gun launched at a speed of 5370 ft/sec and targeted at a steel encased test chamber. The experiment was instrumented with pressure transducers attached to the target chamber, an optical pyrometer to measure temperature, and a high speed digital camera to image the energy release. The cube penetrated the 0.060″ mild steel entrance plate, and then traversed the target chamber to a ¾″ rear plate. The energy release is shown in
FIG. 1 . No increase in pressure or temperature in the chamber was detected. - In this test, a Ta cube with dimensions of ¼″ was gun launched at a speed of 5818 ft/sec and targeted at a steel encased test chamber. The experiment was instrumented with pressure transducers attached to the target chamber, an optical pyrometer to measure temperature, and a high speed digital camera to image the energy release. The cube penetrated the 0.060″ mild steel entrance plate, and then traversed the target chamber to a ¾″ rear plate. The energy release as noted by optical imaging is shown in
FIG. 2 and appears higher than that observed for the steel cube in Example 1. A pressure increase to 2.1 psi was recorded. This is a result of Ta having a greater reactivity with oxygen than steel. The maximum temperature in the chamber was <1500° K. This is the lowest temperature that can be measured. It was estimated that >30% of the original penetrator mass remained on the chamber floor after the test was completed. - In this test, a Zr cube with dimensions of ¼″ was gun launched at a speed of 5297 ft/sec and targeted at a steel encased test chamber. The experiment was instrumented with pressure transducers attached to the target chamber, an optical pyrometer to measure temperature, and a high speed digital camera to image the energy release. The cube penetrated the 0.060″ mild steel entrance plate, and then traversed the target chamber to a ¾″ rear plate. The energy release as noted by optical imaging is shown in
FIG. 3 and appears much higher than that observed for the steel cube in Example 1 or the Ta cube shown in Example 2. A pressure increase to 7.3 psi and a temperature increase to 4500° K were recorded. It was estimated that ˜10% of the original penetrator mass remained on the chamber floor after the test was completed, indicating a high level of reaction. While the Zr had sufficient mass density to penetrate the thin (0.060″) entry plate, it does not have sufficient mass density to penetrate thicker targets for which the penetrator technology is likely to be directed, e.g. missiles or other aircraft or vehicular targets. - An alloy of Ta and Zr was prepared by melting Zr and Ta metals in the arc of a plasma transferred arc (PTA) welding torch and depositing the product in a graphite crucible as shown in
FIG. 4 . A current of 250 amps was used for the PTA torch, which was sufficient to melt both the Ta powder and Zr wire. The molar ratio was approximately 1.3Ta:1Zr. After cooling to room temperature, the alloy was machined into cubes with dimensions of ¼″ by EDM machining. The cubes were gun launched at a speed of 7242 ft/sec and targeted at a steel encased test chamber. The experiment was instrumented with pressure transducers attached to the target chamber, an optical pyrometer to measure temperature, and a high speed digital camera to image the energy release. The cube penetrated the 0.060″ mild steel entrance plate, and then traversed the target chamber to a ¾″ rear plate. The energy release as noted by optical imaging is shown inFIG. 5 , and appears comparable to that obtained for pure Zr in Example 3. A temperature rise to 4800° K was measured in the chamber with a pressure of 12.5 psi. It was estimated that <5% of the original penetrator mass remained on the chamber floor after the test was completed, indicating a very high level of reaction. - A layered composite of Ta and Zr was prepared by depositing a layer of Zr on each side of a ⅛″ Ta plate at a torch amperage of 225 amps. After cooling to room temperature, the alloy was machined into cubes with a dimension of ¼″ by EDM machining. The molar ratio of the Ta and the Zr in the cubes was approximately 1.3Ta:1Zr. The cubes were gun launched at a speed of 6255 ft/sec and targeted at a steel encased test chamber. The experiment was instrumented with pressure transducers attached to the target chamber, an optical pyrometer to measure temperature, and a high speed digital camera to image the energy release. The cube penetrated the 0.060″ mild steel entrance plate, and then traversed the target chamber to a ¾″ rear plate. The energy release as noted by optical imaging is shown in
FIG. 5 . A temperature rise to ˜3800° K was measured in the chamber with a pressure increase of 8.7 psi. It was estimated that ˜20% of the original penetrator mass remained on the chamber floor after the test was completed, indicating a high level of reaction compared to Ta, but lower than for Zr or the Ta/Zr alloy. The incomplete combustion resulted in a lower total energy release than Zr or the Ta/Zr alloy as indicated by the optical micrograph inFIG. 5 . - An alloy of W and Zr was prepared using the experimental setup as shown in
FIG. 4 with a feed of W powder and Zr wire. An amperage for the PTA torch of 280 amps was used which was sufficient to melt both metals. After cooling to room temperature, the alloy was machined into cubes with a dimension of ¼″ by EDM machining. The molar ratio of the W and the Zr in the cubes was approximately 1.3W:1Zr. The cubes were gun launched tested by targeting the penetrator cube at a steel encased test chamber which was instrumented with optical imaging. - A particulate composite of Ta and Zr was prepared using the experimental setup as shown in
FIG. 4 using a feed of Ta powder and Zr wire and with an amperage for the PTA torch of 190 amps. This power level was sufficient to melt the Zr metal but not the Ta powder. After cooling to room temperature, the composite was machined into cubes with a dimension of ¼″ by EDM machining. The molar ratio of the Ta and the Zr in the cubes was approximately 1.3Ta:1Zr. The cubes were gun launched and targeted at a steel encased test chamber which was instrumented with optical imaging. - It should be understood that the preceding is merely a detailed description of certain preferred embodiments of this invention and that numerous changes can be made in accordance with the disclosure herein without departing from the spirit or scope of the invention. The following examples are to be viewed as illustrative of the present invention and should not be viewed as limiting the scope of the invention as defined by the appended claims.
Claims (22)
1. A penetrator comprising a composite material having a uniform structure 1 wherein said composite material comprises at least one high density metal and at least one reactive material.
2. The penetrator of claim 1 , wherein the high density metal is Ta and the reactive material is Zr.
3. The penetrator of claim 1 , wherein the high density metal is selected from the group consisting of Ta, W, Re, Os, Ir, Pt, Au, U, and Hf, and an alloy thereof, and the reactive material is a reactive metal selected from the group consisting of Zr, Mg, Al, Li, Be, Ti, Sc, V, H, Sr, Y, Si, and Ge, and an alloy thereof, a rare earth element and an alloy thereof, hydrogen, carbon and a metal carbide.
4. The penetrator of claim 3 , wherein the rare earth metal is selected from the group consisting of La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb and Lu.
5-7. (canceled)
8. The penetrator of claim 1 , wherein the penetrator has a shape of a cube.
9. (canceled)
10. The penetrator of claim 1 , wherein the reactive material is a reactive metal.
11. The penetrator of claim 1 , wherein the at least one high density metal and the at least one reactive material are bonded by powder metallurgical processing.
12. (canceled)
13. The penetrator of claim 1 , wherein the high density material is in particle form, and a layer of the reactive material is deposited on particles of the high density material.
14. The penetrator of claim 1 , wherein the reactive material is an alloy of at least two reactive metals.
15. The penetrator of claim 1 , wherein at least one of the high density metal and the reactive material comprises a particulate composite.
16. A penetrator consisting essentially of a composite material having at least one constituent comprising at least one high density metal and at least one constituent comprising at least one reactive material.
17. The penetrator of claim 16 , wherein the high density metal is selected from the group consisting of Ta, W, Re, Os, Ir, Pt, Au, U, and Hf, and an alloy thereof, and the reactive material is a reactive metal selected from the group consisting of Zr, Mg, Al, Li, Be, Ti, Sc, V, H, Sr, Y, Si, and Ge, and an alloy thereof, a rare earth element and an alloy thereof, hydrogen, carbon and a metal carbide.
18. The penetrator of claim 17 , wherein the rare earth metal is selected from the group consisting of La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb and Lu.
19. The penetrator of claim 16 , wherein the penetrator has a shape of a cube.
20. The penetrator of claim 16 , wherein the reactive material is a reactive metal.
21. The penetrator of claim 16 , wherein the at least one high density metal and the at least one reactive material are bonded by powder metallurgical processing.
22. The penetrator of claim 16 , wherein the high density material is in particle form, and a layer of the reactive material is deposited on particles of the high density material.
23. The penetrator of claim 16 , wherein the reactive material is an alloy of at least two reactive metals.
24. The penetrator of claim 16 , wherein at least one of the high density metal and the reactive material comprises a particulate composite.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/764,106 US20130199397A1 (en) | 2006-06-19 | 2007-06-15 | Multi component reactive metal penetrators, and their method of manufacture |
| PCT/US2007/071484 WO2013105910A2 (en) | 2006-06-19 | 2007-06-18 | Multi component reactive metal penetrators, and their method of manufacture |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US80512806P | 2006-06-19 | 2006-06-19 | |
| US80512406P | 2006-06-19 | 2006-06-19 | |
| US11/764,106 US20130199397A1 (en) | 2006-06-19 | 2007-06-15 | Multi component reactive metal penetrators, and their method of manufacture |
| US11/764,036 US8573128B2 (en) | 2006-06-19 | 2007-06-15 | Multi component reactive metal penetrators, and their method of manufacture |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US11/764,036 Division US8573128B2 (en) | 2006-06-19 | 2007-06-15 | Multi component reactive metal penetrators, and their method of manufacture |
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| Publication Number | Publication Date |
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| US20130199397A1 true US20130199397A1 (en) | 2013-08-08 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US11/764,106 Abandoned US20130199397A1 (en) | 2006-06-19 | 2007-06-15 | Multi component reactive metal penetrators, and their method of manufacture |
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| US (1) | US20130199397A1 (en) |
| WO (1) | WO2013105910A2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20150268017A1 (en) * | 2014-03-24 | 2015-09-24 | Triple D Tracker | Encrypted spectral taggant for a cartridge |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3946673A (en) * | 1974-04-05 | 1976-03-30 | The United States Of America As Represented By The Secretary Of The Navy | Pyrophoris penetrator |
| US4381692A (en) * | 1977-05-11 | 1983-05-03 | Quantic Industries, Inc. | Method of making an incendiary munition |
| IT1204121B (en) * | 1986-02-27 | 1989-03-01 | Cebora Spa | WELDING TORCH OR PLASMA CUTTING WITH NON-TRANSFERRED ARC |
| US5124122A (en) * | 1989-08-15 | 1992-06-23 | Teledyne Industries, Inc. | Titanium alloy containing prealloyed vanadium and chromium alloy |
| DE69221007T2 (en) * | 1991-04-25 | 1997-11-13 | Nippon Steel Corp | Method and device for applying molten metal coatings |
| US5482672A (en) * | 1995-02-09 | 1996-01-09 | Friedman; Ira | Process for extruding tantalum and/or niobium |
| US5950064A (en) * | 1997-01-17 | 1999-09-07 | Olin Corporation | Lead-free shot formed by liquid phase bonding |
| US20050199323A1 (en) * | 2004-03-15 | 2005-09-15 | Nielson Daniel B. | Reactive material enhanced munition compositions and projectiles containing same |
| US6393991B1 (en) * | 2000-06-13 | 2002-05-28 | General Dynamics Ordnance And Tactical Systems, Inc. | K-charge—a multipurpose shaped charge warhead |
| WO2005036093A2 (en) * | 2003-05-27 | 2005-04-21 | Lockheed Martin Corporation | Spark-producing penetrator and method of using same |
-
2007
- 2007-06-15 US US11/764,106 patent/US20130199397A1/en not_active Abandoned
- 2007-06-18 WO PCT/US2007/071484 patent/WO2013105910A2/en not_active Ceased
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20150268017A1 (en) * | 2014-03-24 | 2015-09-24 | Triple D Tracker | Encrypted spectral taggant for a cartridge |
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| Publication number | Publication date |
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| WO2013105910A2 (en) | 2013-07-18 |
| WO2013105910A3 (en) | 2016-06-09 |
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