US20140013982A1 - Thermite ignition and rusty iron regeneration by localized microwaves - Google Patents
Thermite ignition and rusty iron regeneration by localized microwaves Download PDFInfo
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- US20140013982A1 US20140013982A1 US14/002,740 US201214002740A US2014013982A1 US 20140013982 A1 US20140013982 A1 US 20140013982A1 US 201214002740 A US201214002740 A US 201214002740A US 2014013982 A1 US2014013982 A1 US 2014013982A1
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- mixture
- thermite
- microwave radiation
- chemical reaction
- microwave
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- 239000003832 thermite Substances 0.000 title claims description 102
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 title claims description 31
- 229910052742 iron Inorganic materials 0.000 title claims description 14
- 230000008929 regeneration Effects 0.000 title description 2
- 238000011069 regeneration method Methods 0.000 title description 2
- 239000000203 mixture Substances 0.000 claims abstract description 117
- 238000006243 chemical reaction Methods 0.000 claims abstract description 75
- 238000000034 method Methods 0.000 claims abstract description 49
- 230000005855 radiation Effects 0.000 claims abstract description 46
- 229910052751 metal Inorganic materials 0.000 claims abstract description 28
- 239000002184 metal Substances 0.000 claims abstract description 26
- 239000000463 material Substances 0.000 claims abstract description 14
- 229910044991 metal oxide Inorganic materials 0.000 claims abstract description 13
- 150000004706 metal oxides Chemical class 0.000 claims abstract description 12
- 238000003786 synthesis reaction Methods 0.000 claims abstract description 12
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 11
- 238000005520 cutting process Methods 0.000 claims abstract description 11
- 230000000977 initiatory effect Effects 0.000 claims abstract description 9
- 238000003466 welding Methods 0.000 claims abstract description 6
- 238000005553 drilling Methods 0.000 claims abstract description 4
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 13
- 230000005670 electromagnetic radiation Effects 0.000 claims description 10
- 239000007789 gas Substances 0.000 claims description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 7
- 229910052760 oxygen Inorganic materials 0.000 claims description 7
- 239000001301 oxygen Substances 0.000 claims description 7
- 230000008878 coupling Effects 0.000 claims description 4
- 238000010168 coupling process Methods 0.000 claims description 4
- 238000005859 coupling reaction Methods 0.000 claims description 4
- 239000003153 chemical reaction reagent Substances 0.000 claims description 3
- 239000011148 porous material Substances 0.000 claims description 2
- 238000002485 combustion reaction Methods 0.000 description 17
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 14
- SZVJSHCCFOBDDC-UHFFFAOYSA-N ferrosoferric oxide Chemical compound O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 14
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 14
- 239000000843 powder Substances 0.000 description 12
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 description 10
- 239000010410 layer Substances 0.000 description 10
- SPSSULHKWOKEEL-UHFFFAOYSA-N 2,4,6-trinitrotoluene Chemical compound CC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O SPSSULHKWOKEEL-UHFFFAOYSA-N 0.000 description 9
- 239000000015 trinitrotoluene Substances 0.000 description 9
- 239000004020 conductor Substances 0.000 description 8
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 7
- 229910052681 coesite Inorganic materials 0.000 description 7
- 229910052906 cristobalite Inorganic materials 0.000 description 7
- XMFOQHDPRMAJNU-UHFFFAOYSA-N lead(II,IV) oxide Inorganic materials O1[Pb]O[Pb]11O[Pb]O1 XMFOQHDPRMAJNU-UHFFFAOYSA-N 0.000 description 7
- 239000000377 silicon dioxide Substances 0.000 description 7
- 229910052682 stishovite Inorganic materials 0.000 description 7
- 229910052905 tridymite Inorganic materials 0.000 description 7
- JKQOBWVOAYFWKG-UHFFFAOYSA-N molybdenum trioxide Inorganic materials O=[Mo](=O)=O JKQOBWVOAYFWKG-UHFFFAOYSA-N 0.000 description 6
- 239000007800 oxidant agent Substances 0.000 description 6
- 239000010936 titanium Substances 0.000 description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 239000002360 explosive Substances 0.000 description 5
- 239000000446 fuel Substances 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 239000000919 ceramic Substances 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- 239000004343 Calcium peroxide Substances 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- IWOUKMZUPDVPGQ-UHFFFAOYSA-N barium nitrate Chemical compound [Ba+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O IWOUKMZUPDVPGQ-UHFFFAOYSA-N 0.000 description 2
- ZJRXSAYFZMGQFP-UHFFFAOYSA-N barium peroxide Chemical compound [Ba+2].[O-][O-] ZJRXSAYFZMGQFP-UHFFFAOYSA-N 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- WMWLMWRWZQELOS-UHFFFAOYSA-N bismuth(iii) oxide Chemical compound O=[Bi]O[Bi]=O WMWLMWRWZQELOS-UHFFFAOYSA-N 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- LHJQIRIGXXHNLA-UHFFFAOYSA-N calcium peroxide Chemical compound [Ca+2].[O-][O-] LHJQIRIGXXHNLA-UHFFFAOYSA-N 0.000 description 2
- 235000019402 calcium peroxide Nutrition 0.000 description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000004880 explosion Methods 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- YADSGOSSYOOKMP-UHFFFAOYSA-N lead dioxide Inorganic materials O=[Pb]=O YADSGOSSYOOKMP-UHFFFAOYSA-N 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- GNMQOUGYKPVJRR-UHFFFAOYSA-N nickel(III) oxide Inorganic materials [O-2].[O-2].[O-2].[Ni+3].[Ni+3] GNMQOUGYKPVJRR-UHFFFAOYSA-N 0.000 description 2
- PZFKDUMHDHEBLD-UHFFFAOYSA-N oxo(oxonickeliooxy)nickel Chemical compound O=[Ni]O[Ni]=O PZFKDUMHDHEBLD-UHFFFAOYSA-N 0.000 description 2
- 230000000149 penetrating effect Effects 0.000 description 2
- 239000012286 potassium permanganate Substances 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- MTPVUVINMAGMJL-UHFFFAOYSA-N trimethyl(1,1,2,2,2-pentafluoroethyl)silane Chemical compound C[Si](C)(C)C(F)(F)C(F)(F)F MTPVUVINMAGMJL-UHFFFAOYSA-N 0.000 description 2
- 230000005457 Black-body radiation Effects 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- SNIOPGDIGTZGOP-UHFFFAOYSA-N Nitroglycerin Chemical compound [O-][N+](=O)OCC(O[N+]([O-])=O)CO[N+]([O-])=O SNIOPGDIGTZGOP-UHFFFAOYSA-N 0.000 description 1
- 239000000006 Nitroglycerin Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 229910010293 ceramic material Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000005112 continuous flow technique Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052593 corundum Inorganic materials 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000005474 detonation Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229960003711 glyceryl trinitrate Drugs 0.000 description 1
- 229910052595 hematite Inorganic materials 0.000 description 1
- 239000011019 hematite Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000013461 intermediate chemical Substances 0.000 description 1
- LIKBJVNGSGBSGK-UHFFFAOYSA-N iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Fe+3].[Fe+3] LIKBJVNGSGBSGK-UHFFFAOYSA-N 0.000 description 1
- 239000006249 magnetic particle Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000002114 nanocomposite Substances 0.000 description 1
- 229910001120 nichrome Inorganic materials 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 1
- 230000001902 propagating effect Effects 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000003886 thermite process Methods 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 229910001845 yogo sapphire Inorganic materials 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B33/00—Compositions 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/08—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor
- B01J19/12—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor employing electromagnetic waves
- B01J19/122—Incoherent waves
- B01J19/126—Microwaves
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B5/00—General methods of reducing to metals
- C22B5/02—Dry methods smelting of sulfides or formation of mattes
- C22B5/04—Dry methods smelting of sulfides or formation of mattes by aluminium, other metals or silicon
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/08—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor
- B01J2219/0873—Materials to be treated
- B01J2219/0879—Solid
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/08—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor
- B01J2219/12—Processes employing electromagnetic waves
- B01J2219/1203—Incoherent waves
- B01J2219/1206—Microwaves
- B01J2219/1248—Features relating to the microwave cavity
- B01J2219/1269—Microwave guides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/08—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor
- B01J2219/12—Processes employing electromagnetic waves
- B01J2219/1203—Incoherent waves
- B01J2219/1206—Microwaves
- B01J2219/1287—Features relating to the microwave source
- B01J2219/129—Arrangements thereof
- B01J2219/1293—Single source
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/08—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor
- B01J2219/12—Processes employing electromagnetic waves
- B01J2219/1203—Incoherent waves
- B01J2219/1206—Microwaves
- B01J2219/1287—Features relating to the microwave source
- B01J2219/129—Arrangements thereof
- B01J2219/1296—Multiple sources
Definitions
- Thermite is a general term for exothermic reactions between metals and oxidizers.
- the latter is typically a metal oxide, which utilizes the reduction of the metallic oxide with the metallic element to exhaust a significant amount of heat.
- One of the most common mixtures of thermite powder contains hematite and aluminum, which function as the metal-oxidizer and the metallic element, respectively.
- the final products generated are pure iron, alumina, and heat energy.
- the corresponding chemical formula that describes this reaction is
- thermite adiabatic flame temperature in the example above may reach 4,382 K (reduced though to 3,135 K if including the losses due to the phase change during the process).
- This combustion temperature is found to be much hotter than hydrocarbon-based fuel flame such as Benzene, which has a flame temperature of 2,342 K.
- the thermite combustion temperature is higher than the melting temperatures of its two initial components in separate (1,838 K for iron rust and 933 K for aluminum). Consequently, the combustion of a thermite mixture can be a self propagating process. Due to the intense blackbody radiation emitted by the high-temperature thermite combustion, the thermite reaction can be detected by a radiation detector even at microwave frequencies.
- the bi-molecular thermite reaction rate is limited by diffusion due to the mass transfer mechanism between the metal and the oxidizer particles. Hence this reaction is significantly slow compared to the monomolecular based explosives such as TNT.
- Thermite combustion rate was studied and simulated, and was found to be in the range of ⁇ 0.02-0.05 m/s. This speed is extremely slow compared to the TNT detonation velocity of 6,850 m/s.
- the thermite combustion rate is highly dependent on the contact surface area of the metal and the oxidizer, as determined by the powder particle size (smaller particles cause faster combustion rates). Thus, nano-composite thermite powders benefit a significant increase in the combustion rate value.
- the combustion speed may reach 600-1,000 m/s.
- the ignition time delay can be shortened by two orders of magnitude compared to the micron-sized thermite composites.
- the ferro-thermite components are relatively non toxic, which is not the case for TNT explosives or nitroglycerin.
- the gas phase is absent in the thermite reaction, as can be seen by its chemical formula in Eq. (1), hence the direct blast pressure formed is significantly reduced compared to common explosives.
- TNT for example, releases large amount of gas during a complete balanced decomposition, even though additional oxygen is required as inferred from the following formula
- the pressure fowled can be calculated by the ideal gas formula modified for high pressure values with the co-volume factor ⁇
- V is the volume of the closed test cell
- n is the produced number of gas moles
- T e is the explosion temperature
- R is the molar gas constant.
- Thermite ignition by a conventional flame requires a significant reduction of the ignition temperature, typically by adding oxidizer and binder to the thermite powder.
- the ‘Thermate-TH3’ mixture which is used in AN-M14 incendiary hand grenade of the US army, is composed of 29% barium nitrate (BaN2O6), sulfur, and a binder, added to 68.7% of thermite.
- thermite-based grenades contains a starter mixture composed of 66% potassium nitrate (KNO3) and other materials (for the ignition as enriched oxide source) added to the oxide enriched thermite powder.
- the starter mixture may contain ultra fine thermite powder which is easier to ignite with a hotwire energized by DC current.
- This kind of salt is used as an oxidizing agent that generates enough heat as required to ignite the thermite when it burns. Due to their unique features, thermite powders are used in explosive charges, in devices used for cutting or penetrating metals, and in air-bag system inflators.
- thermite reaction is used in material processing including metals, ceramics, and composite materials. Due to the thermite high combustion temperature, it is utilized also for welding techniques. Thermite based reactions can be utilized for covering iron alloys by an intermediate pure metal and alumina coating, as the ceramic material created by the thermite combustion (note that a centrifugal thermite process uses this feature for making composite steel pipes by filling them with thermite and ignites it while the pipe is rolling around its symmetrical axis).
- the present invention is a method and corresponding devices for employing thermite reactions actuated by localized application of microwaves.
- a method comprising the steps of: (a) providing a mixture of at least a metal oxide and a metal which undergoes an exothermic chemical reaction; and (b) applying microwave radiation to the mixture so as to generate a localized hot spot in the mixture, the localized hot spot having at least one dimension smaller than the wavelength of the microwave radiation, thereby initiating the exothermic chemical reaction.
- the exothermic chemical reaction has an ignition temperature in excess of 1400 degrees Celsius.
- the exothermic chemical, reaction is a thermite reaction.
- the microwave radiation is generated by a microwave source of power less than 2 kW.
- the microwave radiation is generated by a microwave source of power less than 200 W.
- the microwave radiation is generated by a solid-state microwave source.
- the applying is performed by coupling an evanescent field with the mixture.
- the applying is performed using an open ended waveguide as an applicator.
- the applying is performed using a waveguide terminating at one or more slot as an antenna.
- the mixture is deployed so as to achieve cutting, drilling, or welding of adjacent materials when initiated.
- the applying is performed in an oxygen free environment such as underwater.
- the mixture includes rust formed on the surface of an iron-based metal object and a reactive metal such that the chemical reaction is effective to convert the rust to iron.
- the mixture is dynamically added to a reaction region within which the microwave radiation is applied to the mixture during application of the microwave radiation to the mixture.
- the mixture includes at least one gas-generating reagent.
- the applying microwave radiation is performed within a rocket motor arrangement to generate thrust.
- gas pressure is converted to mechanical motion so as to serve as an engine powering a mechanical device.
- the mixture is chosen so that the exothermic reaction performs a self-propagating high-temperature synthesis (SHS) of a porous material.
- SHS self-propagating high-temperature synthesis
- a method comprising the steps of: (a) providing a mixture of at least a metal oxide and a metal which undergoes an exothermic chemical reaction; and (b) applying microwave radiation to the mixture so as to generate heat within the mixture, thereby initiating the exothermic chemical reaction, wherein said microwave radiation is applied in a manner so as to satisfy at least one of the conditions: (i) a hot spot is generated in the mixture, said hot spot having at least one dimension smaller than the wavelength of the microwave radiation; (ii) heat is generated in a region having at least one dimension smaller than the wavelength of the microwave radiation; (iii) a hot spot is generated in a region smaller than a volume of the mixture.
- a method comprising the steps of: (a) providing a mixture of at least a metal oxide and a metal which undergoes an exothermic chemical reaction; and (b) applying electromagnetic radiation having a at one or more frequency in the range of 1 MHz to 1 THz to the mixture so as to generate heat within generate a localized hot spot in the mixture, said localized hot spot having at least one dimension smaller than the wavelength of the electromagnetic radiation, thereby initiating the exothermic chemical reaction, said electromagnetic radiation is applied in a manner so as to satisfy at least one of the conditions: (i) a hot spot is generated in the mixture, said hot spot having at least one dimension smaller than the wavelength of the electromagnetic radiation; (ii) heat is generated in a region having at least one dimension smaller than the wavelength of the electromagnetic radiation; (iii) a hot spot is generated in a region smaller than a volume of the mixture.
- FIG. 1 is an optional block diagram of an embodiment of the present invention for initiating thermite reactions by localized application of microwave radiation;
- FIG. 2 is a schematic representation of a suggested but non-limiting principle of operation of thermite ignition by localized application of microwave radiation according to an aspect of the present invention, illustrated with a coaxial microwave applicator;
- FIGS. 3A and 3B are a schematic isometric and side view, respectively, of a tapered near-field microwave applicator for use in an embodiment of the present invention
- FIG. 4 is a schematic illustration of a slot-type near-field microwave applicator for use in an embodiment of the present invention
- FIG. 5 is a schematic illustration of a strip-line-type near-field microwave applicator for use in an embodiment of the present invention
- FIG. 6A is a schematic isometric view of a device for employing a thermite reaction actuated by localized application of microwaves according to an embodiment of the present invention
- FIG. 6B is a schematic cross-sectional view of the device of FIG. 6A while in use;
- FIG. 7A is a schematic isometric view of a device for employing a thermite reaction actuated by localized application of microwaves according to an embodiment of the present invention serving as a torch;
- FIG. 7B is a schematic isometric view of a device for employing a thermite reaction actuated by localized application of microwaves according to an embodiment of the present invention serving as a torch;
- FIG. 8 is a schematic isometric view of a device for employing a thermite reaction actuated by localized application of microwaves according to an embodiment of the present invention serving as a cutting tool;
- FIG. 9 is a schematic isometric view of a device for employing a thermite reaction actuated by localized application of microwaves according to an embodiment of the present invention serving as a cutting tool;
- FIG. 10 is a schematic isometric view of a device for employing a thermite reaction actuated by localized application of microwaves according to an embodiment of the present invention serving as a cutting tool;
- FIG. 11 is a schematic isometric view of a device for employing a thermite reaction actuated by localized application of microwaves according to an embodiment of the present invention performing rust conversion;
- FIG. 13 is a schematic isometric view of a device for employing a thermite reaction actuated by localized application of microwaves according to an embodiment of the present invention performing material synthesis in batch processing;
- FIG. 14 is a schematic isometric view of a device for employing a thermite reaction actuated by localized application of microwaves according to an embodiment of the present invention performing material synthesis in continuous processing;
- FIG. 15 is a schematic isometric view of a device for employing a thermite reaction actuated by localized application of microwaves according to an embodiment of the present invention operating as a rocket engine;
- FIG. 16 is a schematic representation showing the ignition of a larger volume of thermite by an arrangement of several microwave applicators in an array radiating simultaneously, or sequentially, into the volume to ignite it in several places or in a joint focal point.
- FIG. 1 illustrates schematically a system, generally designated 10 , according to certain embodiments of the present invention, and suitable for implementing certain methods according to the present invention.
- system 10 includes a microwave source 12 that supplies microwave radiation to a waveguide 16 which terminates at an applicator 18 , referred to as a “concentrator”, configured for coupling of near-field microwave radiation into a mixture 20 containing at least a metal oxide and a metal which undergo an exothermic chemical reaction.
- a microwave source 12 that supplies microwave radiation to a waveguide 16 which terminates at an applicator 18 , referred to as a “concentrator”, configured for coupling of near-field microwave radiation into a mixture 20 containing at least a metal oxide and a metal which undergo an exothermic chemical reaction.
- the present invention provides a novel ignition method and corresponding igniter for thermite mixtures without requiring intermediate chemical additives.
- Localized microwave energy has been shown to generate sufficient heat to ignite thermite.
- the hotspot induced intentionally by a relatively low power microwave applicator with a concentrator generates enough heat-per-volume for thermite ignition.
- the invention is described as relating to ignition of a mixture of a metal oxide and a metal which undergoes an exothermic chemical reaction, and particularly, reactions of this type which have a high ignition temperature.
- the invention is implemented with mixtures that undergo exothermic chemical reactions with ignition temperature in excess of 900 degrees Celsius, and more preferably in excess of 1400 degrees Celsius.
- the exothermic chemical reaction is a thermite reaction, namely, a two-component mixture of a metal oxide and a metal, and in certain particularly preferred options, a pure thermite mixture without any additives.
- microwave is used herein in the description and claims, except where otherwise qualified, to refer broadly to the broadest range of electromagnetic radiation normally referred to as “microwave”, and its bordering regions of the spectrum which, for the purpose of the present invention, may be used to achieve similar effects.
- the present invention is applicable for electromagnetic waves in frequencies between ⁇ 1 MHz to ⁇ 1 THz, which overlaps frequencies typically referred to as radio frequencies (RF) and millimeter waves, respectively.
- RF radio frequencies
- Certain particularly preferred implementations employ microwave radiation at frequencies in the range of 300 MHz to 300 GHz (wavelengths of 1 meter to 1 millimeter).
- the entire volume of mixture may be considered the “hot spot” according to the present invention, still being a “spot” in the sense that the radiation is localized into a volume having at least one dimension less than the wavelength.
- the hot spot may not always remain localized within less than a wavelength, but in such cases will be small compared to the volume of the mixture.
- preferred applications of the present invention typically satisfy at least one of the conditions:
- a hot spot is generated in the mixture, the hot spot having at least one dimension smaller than the wavelength of the radiation;
- a hot spot is generated in a region smaller than a volume of the mixture.
- hot spot is used to refer to a localized region or volume within a larger volume within which material is heated significantly above the temperature of the surrounding material.
- the size of the hot spot may conveniently be defined by the full width at half maximum (FWHM), i.e., the dimensions of the region for which the temperature is above 50% of the temperature difference between the peak temperature and the surrounding mixture.
- FWHM full width at half maximum
- the present invention is not limited to the aforementioned low-power implementations.
- Other implementations may, for example, apply power above ⁇ 1 kW, either by a vacuum tube or by employing an array of lower power radiating elements.
- the operating frequency may be any frequency in the microwave range as defined above.
- microwave source 12 is preferably protected by an isolator 14 (optional), which is a standard off-the-shelf component preventing reflected radiation from damaging the microwave source.
- Adjustable matching components 22 may be used to optimize energy delivery to the mixture 20 via applicator 18 .
- FIG. 2 illustrates an implementation of applicator 18 as a coaxial structure including a central conductor 24 extending within an outer conductive sheath 26 .
- Central conductor 24 extends beyond the end of conductive sheath 26 and is in close proximity to, or more preferably immersed in, mixture 20 .
- part or all of the extending portion of central conductor 24 may be protected by a ceramic layer, provided for example as ceramic beads 36 .
- the open end of a coaxial waveguide without projection of the central conductor, or the end of a circular waveguide above cutoff may also be effective as an applicator when brought into close proximity or contact with mixture 20 .
- FIGS. 3A and 3B show an implementation with a tapered waveguide 30 .
- FIG. 4 shows an implementation using a waveguide terminating at one or more slot 32 as an antenna.
- Embodiments of the present invention may be implemented in a range of different configurations to provide a range of different types of functionality, as will now be illustrated with reference to a number of non-limiting examples portrayed in FIGS. 6A-15 .
- FIGS. 6A and 6B show a simple arrangement in which mixture 20 is included within a reaction chamber 40 with an opening 42 formed in its base through which applicator 18 is inserted.
- the mixture is ignited locally at hot-spot 23 adjacent to the end of the applicator, resulting in self-ignition of the entire contents of the reaction chamber and ejecting a flame in region 44 .
- FIGS. 7A and 7B illustrate two non-limiting examples of a thermite-based blow-torch implementation according to the present invention in which mixture 20 is dynamically added to a reaction region within which the microwave radiation is applied to the mixture, thereby providing an ongoing source of intense heat for a variety of applications.
- a microwave input port 46 (typically present in all embodiments of the invention, but not separately labeled) feeds the microwave signal into coaxial waveguide 48 .
- An external thermite source 50 is fed by a flow of air pressure 52 or by some other feed arrangement (not shown) through a metal pipe 54 into coaxial waveguide 48 .
- Pipe 54 is configured to be in microwave cutoff, so the microwave energy cannot propagate through it.
- FIG. 7B is conceptually similar to FIG. 7A , with equivalent elements labeled similarly.
- pipe 54 connects directly to the inner channel of a hollow section of the central conductor 64 of the coaxial waveguide 48 .
- Hot-spot ignition occurs at region 60 , just beyond the end of hollow central conductor 64 , as described above.
- the reaction may or may not be self-propagating.
- switching off of the torch is typically achieved by interrupting both the flow of mixture and the microwave delivery.
- FIGS. 8-10 illustrate a number of non-limiting but preferred examples of implementations of the present invention useful as cutting tools for cutting material.
- flame 62 can be collimated by use of a suitable nozzle shape (not shown).
- the collimation can be done by externally induced magnetic fields. For example, by attaching a permanent magnet to the metallic substrate it can be magnetized. Consequently the flame made of hot magnetic particles can be collimated to the metal substrate by the induced magnetic field.
- the collimation can be done by a coil that surrounds the flame so it induces an axial magnetic field.
- FIG. 9 shows an alternative cutting technique in which thermite mixture 20 is applied to the surface of the body to be cut or otherwise processed, and is then ignited by the system 10 of FIG. 1 using any suitable applicator, such as those discussed above.
- microwave radiation delivered to input port 46 along waveguide 16 via applicator 18 ignites mixture 20 at a hotspot generated in the interaction region 60 , and results in cutting or melting of body 70 at region 72 .
- the ability to ignite a pure thermite mixture conveniently in situ facilitates another particularly preferred aspect of the present invention, namely, a rust conversion technique in which iron can be regenerated from a layer of rust through a thermite reaction which preferably simultaneously generates a protective layer.
- a layer of thermite mixture including the oxide of the substrate metal and an additional metal is applied to the substrate metal which has an oxide (rust) outer layer 76 .
- the mixture is ignited using a device such as was described in FIG. 9 .
- the oxide layer is converted to the final products of the thermite reaction.
- thermite made of rust (Fe 2 O 3 ) and aluminum (Al) that covers an iron or steel body with a rusty layer, converts the outer layer to iron and alumina.
- FIG. 12 illustrates a system and technique similar to that of FIG. 11 , but in which an entire surface is treated by covering in a layer of the thermite mixture 20 and then moving the igniter device progressively across the region (represented by arrow 78 ) to ensure ignition of the thermite layer across the entire surface.
- the resulted layer of regenerated iron and alumina is designated 80 .
- FIGS. 13 and 14 illustrate processes for production of materials with particular mechanical or chemical properties by self-propagating high-temperature synthesis (SHS) methods.
- SHS high-temperature synthesis
- One particularly preferred example is synthesis of porous ferrite.
- the production process may be either a batch process ( FIG. 13 ) or a continuous process ( FIG. 14 ).
- a microwave igniter such as that of FIG. 9 ignites the mixture 20 located in a mold 82 .
- the mixture may be either pure thermite powder or may contain other materials that interact with the byproducts of the thermite reaction. For example, 3TiO 2 +3C+4Al ⁇ 3TiC+2Al 2 O 3 .
- the reaction between titania (TiO2) and aluminum (Al) is a thermite reaction.
- the titanium (Ti) reacts with the carbon (C) to produce titanium carbide (TiC).
- the ignition temperature of this synthesis reaction is 900 C.
- FIG. 14 illustrates a continuous flow process in which the microwave igniter ignites the mixture 20 in interaction region 60 .
- the mixture is placed on a moving conveyer 84 which feeds it under igniter 10 , continuously generating the desired product 86 .
- certain embodiments of devices and methods according to the present invention employ mixtures 20 which include at least one gas-generating reagent.
- the device then becomes a thermite-fueled thrust-generating device, which may be used directly in a rocket engine, or may be employed with a piston arrangement or other device for converting gas pressure to mechanical motion, as a combustion engine, in order to power a mechanical device.
- FIG. 15 shows schematically a non-limiting example of a thermite-fueled thrust-generating device according to this aspect of the present invention in which a mixer 90 mixes thermite powder mixture 20 with carbon 92 .
- This mixture is fed into a microwave igniter 94 that utilizes a near-field applicator to ignite the thermite in the mixture by microwave energy.
- the added carbon is incinerated with the oxygen in the air, or with additional metal oxide that produces extra oxygen, for a balanced chemical reaction.
- the generated byproducts are emitted outside through a dedicated exhaust 96 .
- the high pressure gas produced generate the thrust 98 .
- An external rocket engine or a piston utilizes the emitted thrust to generate mechanical power and motion.
- FIG. 16 this illustrates schematically a further set of implementations of the present invention according to which a plurality of microwave applicators 100 , constructed according to any of the above examples, are used as an array 101 or otherwise coordinated to generate one or more ignition hot-spot 102 within a mixture 99 .
- This approach may be valuable in a wide range of applications including, but not limited to: coordinated heating of a single hot-spot by a plurality of applicators in order to achieve higher overall power, or to reach a greater depth, than would be achieved by a single applicator; simultaneous multi-point ignition of a large quantity, or geometrical extent, of mixture at spaced-apart locations; and sequential ignition of mixture at spaced-apart locations in order to achieve a particular ignition sequence or sequential processing of different regions.
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Abstract
A method and corresponding devices employ a mixture of at least a metal oxide and a metal which undergoes an exothermic chemical reaction. Microwave radiation is applied to the mixture so as to generate a localized hot spot in the mixture, thereby initiating the exothermic chemical reaction. The use of localized microwave radiation facilitates low power and portable implementations. Devices and techniques for cutting, drilling, welding, material synthesis, generating thrust, and mechanical power and motion are also disclosed.
Description
- Thermite is a general term for exothermic reactions between metals and oxidizers. The latter is typically a metal oxide, which utilizes the reduction of the metallic oxide with the metallic element to exhaust a significant amount of heat. One of the most common mixtures of thermite powder contains hematite and aluminum, which function as the metal-oxidizer and the metallic element, respectively. The final products generated are pure iron, alumina, and heat energy. The corresponding chemical formula that describes this reaction is
-
Fe2O3+2Al→2Fe+Al2O3+Qheat, (1) - where the heat energy released Qheat is 3.947 kJ/g in this reaction (for the sake of comparison, the heat released in trinitrotoluene (TNT) explosion is 4.247 kJ/g theoretically). Furthermore, the thermite adiabatic flame temperature in the example above may reach 4,382 K (reduced though to 3,135 K if including the losses due to the phase change during the process). This combustion temperature is found to be much hotter than hydrocarbon-based fuel flame such as Benzene, which has a flame temperature of 2,342 K. Moreover, the thermite combustion temperature is higher than the melting temperatures of its two initial components in separate (1,838 K for iron rust and 933 K for aluminum). Consequently, the combustion of a thermite mixture can be a self propagating process. Due to the intense blackbody radiation emitted by the high-temperature thermite combustion, the thermite reaction can be detected by a radiation detector even at microwave frequencies.
- The bi-molecular thermite reaction rate is limited by diffusion due to the mass transfer mechanism between the metal and the oxidizer particles. Hence this reaction is significantly slow compared to the monomolecular based explosives such as TNT. Thermite combustion rate was studied and simulated, and was found to be in the range of ˜0.02-0.05 m/s. This speed is extremely slow compared to the TNT detonation velocity of 6,850 m/s. The thermite combustion rate is highly dependent on the contact surface area of the metal and the oxidizer, as determined by the powder particle size (smaller particles cause faster combustion rates). Thus, nano-composite thermite powders benefit a significant increase in the combustion rate value. In a thermite mixture of Al—MoO3 for instance the combustion speed may reach 600-1,000 m/s. In addition, the ignition time delay can be shortened by two orders of magnitude compared to the micron-sized thermite composites. Except that the inhalation of any thin powder should be avoided, the ferro-thermite components are relatively non toxic, which is not the case for TNT explosives or nitroglycerin.
- The gas phase is absent in the thermite reaction, as can be seen by its chemical formula in Eq. (1), hence the direct blast pressure formed is significantly reduced compared to common explosives. TNT for example, releases large amount of gas during a complete balanced decomposition, even though additional oxygen is required as inferred from the following formula
-
2C2H5N3O6→14CO2+5H2O+3N2−21O (2) - The pressure fowled can be calculated by the ideal gas formula modified for high pressure values with the co-volume factor α
-
- where V is the volume of the closed test cell, n is the produced number of gas moles, Te is the explosion temperature, and R is the molar gas constant. When oxygen is lack and the TNT decomposition is not balanced, the generated gas is reduced and it contains different kinds of molecules such as carbon monoxide and hydrogen according to Kistiakowsky-Wilson rules. While the oxygen has to come from an external source in TNT and in other conventional hydrocarbon based fuels, it is an inherent component in the thermite mixture, and it is sufficient for a balanced combustion. As a result, the thermite fuel can be incinerated at oxygen-free environments, such as underwater operations. In addition, thermite as a fuel can be used as a “clean” energy source; due to the lack of carbon molecules it never emits carbon monoxide contamination.
- The thermite ignition temperature is higher than 1500° C. for the Fe2O3—Al thermite mixture. However, for the nanometer-size thermite mixtures, the ignition temperature, as one of their superior properties, can reach as low as 410° C. as super-thermite. This temperature is derived from the high melting temperature of the ingredients which is extremely high as opposed to TNT which requires a temperature of only 300° C. to be ignited. This fact makes the thermite mixture more stable, but also harder to ignite, thus a suitable igniter is required for this kind of metal fuel. The ignition of the thermite mixture above can be achieved by a laser beam for MoO3—Al and Fe2O3—Al thermite mixture. Microwave ignition has been reported in the literature, but it involved a microwave pulse of high power (>50 kW) and high frequency (75 GHz) from a gyrotron. Other microwave schemes were proposed for heating energetic materials.
- Thermite ignition by a conventional flame requires a significant reduction of the ignition temperature, typically by adding oxidizer and binder to the thermite powder. For example the ‘Thermate-TH3’ mixture, which is used in AN-M14 incendiary hand grenade of the US army, is composed of 29% barium nitrate (BaN2O6), sulfur, and a binder, added to 68.7% of thermite. Furthermore, thermite-based grenades contains a starter mixture composed of 66% potassium nitrate (KNO3) and other materials (for the ignition as enriched oxide source) added to the oxide enriched thermite powder. The starter mixture may contain ultra fine thermite powder which is easier to ignite with a hotwire energized by DC current.
- In the absence of an oxidizer in the intermediate starting mixture, it is almost impossible to initiate the thermite combustion in a closed can, even with a Nichrome hotwire energized by electric current (melted at 1,400° C.). Hence, calcium peroxide (CaO2) is added in order to lower the ignition temperature and enable the mixture ignition. Another method to ignite a thermite mixture is by adding barium peroxide (BaO2) to the thermite and lighten it by a magnesium ribbon. Yet, it is a dangerous process since it is hard to control the magnesium combustion. Alternatively the magnesium can be replaced by potassium permanganate (KMnO4) with glycerin. This kind of salt is used as an oxidizing agent that generates enough heat as required to ignite the thermite when it burns. Due to their unique features, thermite powders are used in explosive charges, in devices used for cutting or penetrating metals, and in air-bag system inflators.
- Except for its explosive features, the thermite reaction is used in material processing including metals, ceramics, and composite materials. Due to the thermite high combustion temperature, it is utilized also for welding techniques. Thermite based reactions can be utilized for covering iron alloys by an intermediate pure metal and alumina coating, as the ceramic material created by the thermite combustion (note that a centrifugal thermite process uses this feature for making composite steel pipes by filling them with thermite and ignites it while the pipe is rolling around its symmetrical axis).
- There is also a special need to ignite small quantities of pure thermite, which is usually less efficient by conventional ignition techniques because of the relatively large igniter needed (possibly even larger the thermite mixture itself). Small-quantity thermite applications could be useful for example in thermite welding of small parts, or for small-scale material synthesis by the thermite combustion (e.g. for production of alumina and iron as in Eq. (1)).
- There are therefore various needs for methods and corresponding devices for employing thermite reactions actuated by localized application of microwaves.
- The present invention is a method and corresponding devices for employing thermite reactions actuated by localized application of microwaves.
- According to the teachings of the present invention there is provided, a method comprising the steps of: (a) providing a mixture of at least a metal oxide and a metal which undergoes an exothermic chemical reaction; and (b) applying microwave radiation to the mixture so as to generate a localized hot spot in the mixture, the localized hot spot having at least one dimension smaller than the wavelength of the microwave radiation, thereby initiating the exothermic chemical reaction.
- According to an embodiment of the present invention, the exothermic chemical reaction has an ignition temperature in excess of 900 degrees Celsius.
- According to an embodiment of the present invention, the exothermic chemical reaction has an ignition temperature in excess of 1400 degrees Celsius.
- According to an embodiment of the present invention, the exothermic chemical, reaction is a thermite reaction.
- According to an embodiment of the present invention, the microwave radiation is generated by a microwave source of power less than 2 kW.
- According to an embodiment of the present invention, the microwave radiation is generated by a microwave source of power less than 200 W.
- According to an embodiment of the present invention, the microwave radiation is generated by a solid-state microwave source.
- According to an embodiment of the present invention, the applying is performed by coupling an evanescent field with the mixture.
- According to an embodiment of the present invention, the applying is performed using an open ended waveguide as an applicator.
- According to an embodiment of the present invention, the applying is performed using a waveguide terminating at one or more slot as an antenna.
- According to an embodiment of the present invention, the mixture is deployed so as to achieve cutting, drilling, or welding of adjacent materials when initiated.
- According to an embodiment of the present invention, the applying is performed in an oxygen free environment such as underwater.
- According to an embodiment of the present invention, the mixture includes rust formed on the surface of an iron-based metal object and a reactive metal such that the chemical reaction is effective to convert the rust to iron.
- According to an embodiment of the present invention, the mixture is dynamically added to a reaction region within which the microwave radiation is applied to the mixture during application of the microwave radiation to the mixture.
- According to an embodiment of the present invention, the mixture includes at least one gas-generating reagent.
- According to an embodiment of the present invention, the applying microwave radiation is performed within a rocket motor arrangement to generate thrust.
- According to an embodiment of the present invention, gas pressure is converted to mechanical motion so as to serve as an engine powering a mechanical device.
- According to an embodiment of the present invention, the mixture is chosen so that the exothermic reaction performs a self-propagating high-temperature synthesis (SHS) of a porous material.
- There is also provided according to the teachings of an embodiment of the present invention, a method comprising the steps of: (a) providing a mixture of at least a metal oxide and a metal which undergoes an exothermic chemical reaction; and (b) applying microwave radiation to the mixture so as to generate heat within the mixture, thereby initiating the exothermic chemical reaction, wherein said microwave radiation is applied in a manner so as to satisfy at least one of the conditions: (i) a hot spot is generated in the mixture, said hot spot having at least one dimension smaller than the wavelength of the microwave radiation; (ii) heat is generated in a region having at least one dimension smaller than the wavelength of the microwave radiation; (iii) a hot spot is generated in a region smaller than a volume of the mixture.
- There is also provided according to the teachings of an embodiment of the present invention, a method comprising the steps of: (a) providing a mixture of at least a metal oxide and a metal which undergoes an exothermic chemical reaction; and (b) applying electromagnetic radiation having a at one or more frequency in the range of 1 MHz to 1 THz to the mixture so as to generate heat within generate a localized hot spot in the mixture, said localized hot spot having at least one dimension smaller than the wavelength of the electromagnetic radiation, thereby initiating the exothermic chemical reaction, said electromagnetic radiation is applied in a manner so as to satisfy at least one of the conditions: (i) a hot spot is generated in the mixture, said hot spot having at least one dimension smaller than the wavelength of the electromagnetic radiation; (ii) heat is generated in a region having at least one dimension smaller than the wavelength of the electromagnetic radiation; (iii) a hot spot is generated in a region smaller than a volume of the mixture.
- The invention is herein described, by way of example only, with reference to the accompanying drawings, wherein:
-
FIG. 1 is an optional block diagram of an embodiment of the present invention for initiating thermite reactions by localized application of microwave radiation; -
FIG. 2 is a schematic representation of a suggested but non-limiting principle of operation of thermite ignition by localized application of microwave radiation according to an aspect of the present invention, illustrated with a coaxial microwave applicator; -
FIGS. 3A and 3B are a schematic isometric and side view, respectively, of a tapered near-field microwave applicator for use in an embodiment of the present invention; -
FIG. 4 is a schematic illustration of a slot-type near-field microwave applicator for use in an embodiment of the present invention; -
FIG. 5 is a schematic illustration of a strip-line-type near-field microwave applicator for use in an embodiment of the present invention; -
FIG. 6A is a schematic isometric view of a device for employing a thermite reaction actuated by localized application of microwaves according to an embodiment of the present invention; -
FIG. 6B is a schematic cross-sectional view of the device ofFIG. 6A while in use; -
FIG. 7A is a schematic isometric view of a device for employing a thermite reaction actuated by localized application of microwaves according to an embodiment of the present invention serving as a torch; -
FIG. 7B is a schematic isometric view of a device for employing a thermite reaction actuated by localized application of microwaves according to an embodiment of the present invention serving as a torch; -
FIG. 8 is a schematic isometric view of a device for employing a thermite reaction actuated by localized application of microwaves according to an embodiment of the present invention serving as a cutting tool; -
FIG. 9 is a schematic isometric view of a device for employing a thermite reaction actuated by localized application of microwaves according to an embodiment of the present invention serving as a cutting tool; -
FIG. 10 is a schematic isometric view of a device for employing a thermite reaction actuated by localized application of microwaves according to an embodiment of the present invention serving as a cutting tool; -
FIG. 11 is a schematic isometric view of a device for employing a thermite reaction actuated by localized application of microwaves according to an embodiment of the present invention performing rust conversion; -
FIG. 12 is a schematic isometric view of a device for employing a thermite reaction actuated by localized application of microwaves according to an embodiment of the present invention performing rust conversion; -
FIG. 13 is a schematic isometric view of a device for employing a thermite reaction actuated by localized application of microwaves according to an embodiment of the present invention performing material synthesis in batch processing; -
FIG. 14 is a schematic isometric view of a device for employing a thermite reaction actuated by localized application of microwaves according to an embodiment of the present invention performing material synthesis in continuous processing; -
FIG. 15 is a schematic isometric view of a device for employing a thermite reaction actuated by localized application of microwaves according to an embodiment of the present invention operating as a rocket engine; and -
FIG. 16 is a schematic representation showing the ignition of a larger volume of thermite by an arrangement of several microwave applicators in an array radiating simultaneously, or sequentially, into the volume to ignite it in several places or in a joint focal point. - The present invention is a method and corresponding devices for employing thermite reactions actuated by localized application of microwaves.
- The principles and operation of methods and devices according to the present invention may be better understood with reference to the drawings and the accompanying description.
- Referring now to the drawings,
FIG. 1 illustrates schematically a system, generally designated 10, according to certain embodiments of the present invention, and suitable for implementing certain methods according to the present invention. Generally speaking,system 10 includes amicrowave source 12 that supplies microwave radiation to awaveguide 16 which terminates at anapplicator 18, referred to as a “concentrator”, configured for coupling of near-field microwave radiation into amixture 20 containing at least a metal oxide and a metal which undergo an exothermic chemical reaction. As illustrated schematically inFIG. 2 ,applicator 18 is configured to localize delivery of the microwave radiation so as to generate a localizedhot spot 23 inmixture 20, the localized hot spot having at least one dimension smaller than a wavelength of the microwave radiation and/or being smaller than the volume of the mixture, thereby initiating the exothermic chemical reaction. - Thus, the present invention provides a novel ignition method and corresponding igniter for thermite mixtures without requiring intermediate chemical additives. Localized microwave energy has been shown to generate sufficient heat to ignite thermite. Instead of lowering the ignition temperature of the thermite, the hotspot induced intentionally by a relatively low power microwave applicator with a concentrator generates enough heat-per-volume for thermite ignition.
- Since no starter mixture is required in order to achieve ignition of a thermite mixture according to the present invention, the invention provides a viable solution for situations where small quantities of mixture (particularly pure thermite) are to be ignited. Thus, in certain preferred applications, the method of the present invention is used to ignite a quantity of thermite mixture of less than 10 g, and in certain cases, less than 1 g.
- On the other hand, the present invention is also scalable for igniting large quantities of thermite mixture. Larger quantities may range from 10 g up to 1000 g, and in certain preferred cases, more than 1 kg. In certain cases, it may be advantageous to employ a penetrating applicator for delivering the microwave radiation to a location within the volume of the mixture. In other cases, it may be advantageous to employ simultaneous delivery of microwave radiation at several locations, such as will be described below with reference to
FIG. 16 . - According to another aspect of the invention, the microwave igniter is used for the removal of rust by iron regeneration. This reaction is achieved by local thermite combustion of rust and aluminum powder ignited by the microwave igniter. The regenerated iron and alumina obtained as the final products can be used to coat the originally rusted object. These and other aspects of the present invention will be better understood by reference to the following detailed description and accompanying drawings.
- At this stage, it will be helpful to define certain terminology as used herein in the description and claims. The invention is described as relating to ignition of a mixture of a metal oxide and a metal which undergoes an exothermic chemical reaction, and particularly, reactions of this type which have a high ignition temperature. Preferably, the invention is implemented with mixtures that undergo exothermic chemical reactions with ignition temperature in excess of 900 degrees Celsius, and more preferably in excess of 1400 degrees Celsius. In certain particularly preferred but non-limiting implementations, the exothermic chemical reaction is a thermite reaction, namely, a two-component mixture of a metal oxide and a metal, and in certain particularly preferred options, a pure thermite mixture without any additives.
- The use of pure thermite mixture which is facilitated by the present invention makes available a range of additional applications which would either otherwise not be feasible due to the need for expensive and bulky high-energy equipment to initiate the reaction according to conventional techniques.
- The general term “microwave” is used herein in the description and claims, except where otherwise qualified, to refer broadly to the broadest range of electromagnetic radiation normally referred to as “microwave”, and its bordering regions of the spectrum which, for the purpose of the present invention, may be used to achieve similar effects. In quantitative terms, the present invention is applicable for electromagnetic waves in frequencies between ˜1 MHz to ˜1 THz, which overlaps frequencies typically referred to as radio frequencies (RF) and millimeter waves, respectively. Certain particularly preferred implementations employ microwave radiation at frequencies in the range of 300 MHz to 300 GHz (wavelengths of 1 meter to 1 millimeter). In some cases, where the wavelength is longer than the dimensions of the volume of the mixture to be ignited, the entire volume of mixture may be considered the “hot spot” according to the present invention, still being a “spot” in the sense that the radiation is localized into a volume having at least one dimension less than the wavelength. In cases of very small wavelengths, the hot spot may not always remain localized within less than a wavelength, but in such cases will be small compared to the volume of the mixture. Thus, preferred applications of the present invention typically satisfy at least one of the conditions:
- (i) a hot spot is generated in the mixture, the hot spot having at least one dimension smaller than the wavelength of the radiation;
- (ii) heat is generated in a region having at least one dimension smaller than the wavelength of the radiation;
- (iii) a hot spot is generated in a region smaller than a volume of the mixture.
- In this context, the term “hot spot” is used to refer to a localized region or volume within a larger volume within which material is heated significantly above the temperature of the surrounding material. The size of the hot spot may conveniently be defined by the full width at half maximum (FWHM), i.e., the dimensions of the region for which the temperature is above 50% of the temperature difference between the peak temperature and the surrounding mixture.
- According to certain preferred implementations of the present invention, the microwave source is a relatively low power source, typically generating no more than 2 kW, and in certain particularly preferred implementations, no more than 200 W. Also according to certain preferred embodiments, the frequency used is also preferably a relatively low frequency in the microwave range (typically 2.45 GHz). Despite this low power and low frequency, as a result of the concentration of the radiation into a small volume, sufficient localized heating is achieved to generate a localized hot spot at high enough temperature to ignite the reaction. The low power requirements enable the use of a solid-state microwave source, thereby making it feasible to implement the system as a compact and light-weight portable device.
- It should be appreciated, however, that the present invention is not limited to the aforementioned low-power implementations. Other implementations may, for example, apply power above ˜1 kW, either by a vacuum tube or by employing an array of lower power radiating elements. Furthermore, the operating frequency may be any frequency in the microwave range as defined above.
- As shown in
FIG. 1 ,microwave source 12 is preferably protected by an isolator 14 (optional), which is a standard off-the-shelf component preventing reflected radiation from damaging the microwave source. Adjustable matching components 22 (optional) may be used to optimize energy delivery to themixture 20 viaapplicator 18. - A wide range of structures may be used to implement
applicator 18 of the present invention.Applicator 18 may be implemented either as an antenna located adjacent to, or immersed in,mixture 20, or may be implemented employing coupling of an evanescent field at the termination of a non-radiating waveguide with the mixture. - By way of a first non-limiting example,
FIG. 2 illustrates an implementation ofapplicator 18 as a coaxial structure including acentral conductor 24 extending within an outerconductive sheath 26.Central conductor 24 extends beyond the end ofconductive sheath 26 and is in close proximity to, or more preferably immersed in,mixture 20. Optionally, as illustrated below inFIG. 6A , part or all of the extending portion ofcentral conductor 24 may be protected by a ceramic layer, provided for example asceramic beads 36. It should be note that, in some cases, the open end of a coaxial waveguide without projection of the central conductor, or the end of a circular waveguide above cutoff may also be effective as an applicator when brought into close proximity or contact withmixture 20. - A further non-limiting example of
applicator 18 is illustrated inFIGS. 3A and 3B which show an implementation with a taperedwaveguide 30. - A further non-limiting example of
applicator 18 is illustrated inFIG. 4 which shows an implementation using a waveguide terminating at one ormore slot 32 as an antenna. - A further non-limiting example of
applicator 18 is illustrated inFIG. 5 which shows an implementation using an open ended waveguide, in this case with a protrudingcentral stripline conductor 34, as an applicator. - Embodiments of the present invention may be implemented in a range of different configurations to provide a range of different types of functionality, as will now be illustrated with reference to a number of non-limiting examples portrayed in
FIGS. 6A-15 . - Referring to
FIGS. 6A and 6B , these show a simple arrangement in whichmixture 20 is included within areaction chamber 40 with anopening 42 formed in its base through whichapplicator 18 is inserted. The mixture is ignited locally at hot-spot 23 adjacent to the end of the applicator, resulting in self-ignition of the entire contents of the reaction chamber and ejecting a flame inregion 44. -
FIGS. 7A and 7B illustrate two non-limiting examples of a thermite-based blow-torch implementation according to the present invention in whichmixture 20 is dynamically added to a reaction region within which the microwave radiation is applied to the mixture, thereby providing an ongoing source of intense heat for a variety of applications. In the example ofFIG. 7A , a microwave input port 46 (typically present in all embodiments of the invention, but not separately labeled) feeds the microwave signal intocoaxial waveguide 48. Anexternal thermite source 50 is fed by a flow of air pressure 52 or by some other feed arrangement (not shown) through ametal pipe 54 intocoaxial waveguide 48.Pipe 54 is configured to be in microwave cutoff, so the microwave energy cannot propagate through it. A thinceramic disc 56 blocks thermite mixture from moving up the waveguide, but allows the microwave radiation to pass through it. Thethermite powder 20 passes through the hollowcoaxial waveguide 48 towards anozzle 58. The high microwave power density in this vicinity of thetip 60 of the central conductor ignites the mixture, and consequently aflame 62 is ejected fromnozzle 58. -
FIG. 7B is conceptually similar toFIG. 7A , with equivalent elements labeled similarly. In this case,pipe 54 connects directly to the inner channel of a hollow section of thecentral conductor 64 of thecoaxial waveguide 48. Hot-spot ignition occurs atregion 60, just beyond the end of hollowcentral conductor 64, as described above. - Depending upon the density of the thermite mixture flow, the reaction may or may not be self-propagating. In both torch implementations, switching off of the torch is typically achieved by interrupting both the flow of mixture and the microwave delivery.
- Turning now to
FIGS. 8-10 , these illustrate a number of non-limiting but preferred examples of implementations of the present invention useful as cutting tools for cutting material. - The example of
FIG. 8 is based on athermite torch 68, which may be implemented according to any ofFIGS. 6A , 7A or 7B.Torch 68 has amicrowave input port 46, a source of thermite 50 (unless pre-loaded according toFIG. 6A ), and generates anoutput flame 62 towards thebody 70 to be cut or otherwise processed, for example, forming acut 72. - According to preferred but non-limiting option,
flame 62 can be collimated by use of a suitable nozzle shape (not shown). Additionally, or alternatively, for magnetic thermite powder, such as Fe3O4—Al, the collimation can be done by externally induced magnetic fields. For example, by attaching a permanent magnet to the metallic substrate it can be magnetized. Consequently the flame made of hot magnetic particles can be collimated to the metal substrate by the induced magnetic field. Alternately, the collimation can be done by a coil that surrounds the flame so it induces an axial magnetic field. - Turning now to
FIG. 9 , this shows an alternative cutting technique in whichthermite mixture 20 is applied to the surface of the body to be cut or otherwise processed, and is then ignited by thesystem 10 ofFIG. 1 using any suitable applicator, such as those discussed above. Thus, microwave radiation delivered to inputport 46 alongwaveguide 16 viaapplicator 18 ignitesmixture 20 at a hotspot generated in theinteraction region 60, and results in cutting or melting ofbody 70 atregion 72. -
FIG. 10 shows an arrangement essentially similar toFIG. 9 , and similarly labeled, but in which the thermite mixture is initially at least partially located within a preformednotch 74 formed in the body. - These devices and techniques described here may also be used for drilling holes, or for welding together two initially separate bodies.
- Turning now to
FIGS. 11 and 12 , the ability to ignite a pure thermite mixture conveniently in situ facilitates another particularly preferred aspect of the present invention, namely, a rust conversion technique in which iron can be regenerated from a layer of rust through a thermite reaction which preferably simultaneously generates a protective layer. As illustrated inFIG. 11 , a layer of thermite mixture including the oxide of the substrate metal and an additional metal is applied to the substrate metal which has an oxide (rust)outer layer 76. The mixture is ignited using a device such as was described inFIG. 9 . After the thermite is ignited, the oxide layer is converted to the final products of the thermite reaction. For example, thermite made of rust (Fe2O3) and aluminum (Al) that covers an iron or steel body with a rusty layer, converts the outer layer to iron and alumina. -
FIG. 12 illustrates a system and technique similar to that ofFIG. 11 , but in which an entire surface is treated by covering in a layer of thethermite mixture 20 and then moving the igniter device progressively across the region (represented by arrow 78) to ensure ignition of the thermite layer across the entire surface. The resulted layer of regenerated iron and alumina is designated 80. - Turning now to
FIGS. 13 and 14 , these illustrate processes for production of materials with particular mechanical or chemical properties by self-propagating high-temperature synthesis (SHS) methods. One particularly preferred example is synthesis of porous ferrite. The production process may be either a batch process (FIG. 13 ) or a continuous process (FIG. 14 ). - According to the option of
FIG. 13 , a microwave igniter such as that ofFIG. 9 ignites themixture 20 located in amold 82. The mixture may be either pure thermite powder or may contain other materials that interact with the byproducts of the thermite reaction. For example, 3TiO2+3C+4Al→3TiC+2Al2O3. The reaction between titania (TiO2) and aluminum (Al) is a thermite reaction. The titanium (Ti) reacts with the carbon (C) to produce titanium carbide (TiC). The ignition temperature of this synthesis reaction is 900 C. -
FIG. 14 illustrates a continuous flow process in which the microwave igniter ignites themixture 20 ininteraction region 60. The mixture is placed on a moving conveyer 84 which feeds it underigniter 10, continuously generating the desired product 86. - Turning now to
FIG. 15 , according to a further option, certain embodiments of devices and methods according to the presentinvention employ mixtures 20 which include at least one gas-generating reagent. The device then becomes a thermite-fueled thrust-generating device, which may be used directly in a rocket engine, or may be employed with a piston arrangement or other device for converting gas pressure to mechanical motion, as a combustion engine, in order to power a mechanical device. - Structurally,
FIG. 15 shows schematically a non-limiting example of a thermite-fueled thrust-generating device according to this aspect of the present invention in which a mixer 90 mixesthermite powder mixture 20 withcarbon 92. This mixture is fed into amicrowave igniter 94 that utilizes a near-field applicator to ignite the thermite in the mixture by microwave energy. The added carbon is incinerated with the oxygen in the air, or with additional metal oxide that produces extra oxygen, for a balanced chemical reaction. The generated byproducts are emitted outside through adedicated exhaust 96. The high pressure gas produced generate thethrust 98. An external rocket engine or a piston utilizes the emitted thrust to generate mechanical power and motion. - Turning finally to
FIG. 16 , this illustrates schematically a further set of implementations of the present invention according to which a plurality ofmicrowave applicators 100, constructed according to any of the above examples, are used as anarray 101 or otherwise coordinated to generate one or more ignition hot-spot 102 within amixture 99. This approach may be valuable in a wide range of applications including, but not limited to: coordinated heating of a single hot-spot by a plurality of applicators in order to achieve higher overall power, or to reach a greater depth, than would be achieved by a single applicator; simultaneous multi-point ignition of a large quantity, or geometrical extent, of mixture at spaced-apart locations; and sequential ignition of mixture at spaced-apart locations in order to achieve a particular ignition sequence or sequential processing of different regions. - The following is an incomplete list of thermite mixtures to which the teachings of the present invention are believed to be applicable:
- 2Al+3AgO, 2AL+3Ag2O, 2Al+B2O3, 2Al+Bi2O3, 2Al+3CoO, 8Al+3Co3O4, 2Al+Cr2O3, 2Al+3CuO, 2Al+3Cu2O, 2Al+Fe2O, 8Al+3Fe3O4, 2Al+3HgO, 10Al+3I2O5, 4Al+3MnO2, 2Al+MoO3, 10Al+3Nb2O5, 2Al+3NiO, 2Al+Ni2O3, 2Al+3PbO, 4Al+3PbO2, 8Al+3Pb3O4, 2Al+3PdO, 4Al+3SiO2, 2Al+3SnO, 4Al+3SnO2, 10Al+3Ta2O5, 4Al+3TiO2, 16Al+3U3O8, 10Al+3V2O5, 4Al+3WO2, 2Al+WO3,
2B+Cr2O3, 2B+3CuO, 2B+Fe2O3, 8B+3Fe3O4, 4B+3MnO2, 8B+3Pb3O4, 3Be+B2O3, 3Be+Cr2O3, Be+CuO, 3Be+Fe2O3, 4Be+Fe3O4, 2Be+MnO2, 2Be+PbO2, 4Be+Pb3O4, 2Be+SiO2,
3Hf+2B2O3, 3Hf+2Cr2O3, Hf+2CuO, 3Hf+2Fe2O3, 2Hf+Fe3O4, Hf+MnO2, 2Hf+Pb3O4, Hf+SiO2,
2La+3AgO, 2La+3CuO, 2La+Fe2O3, 2La+3HgO, 10La+2I2O5, 4La+3MnO2, 2La+3PbO, 4La+3PbO2, 8La+3Pb3O4, 2La+3PdO, 4La+3WO2, 2La+WO3,
6Li+B2O3, 6Li+Cr2O3, 2Li+CuO, 6Li+Fe2O3, 8Li+Fe3O4, 4Li+MnO2, 6Li+MoO38Li+Pb3O4, 4Li+SiO2, 6Li+WO3,
3Mg+B2O3, 3Mg+Cr2O3, Mg+CuO, 3Mg+Fe2O3, 4Mg+Fe3O4, 2Mg+MnO2, 4Mg+Pb3O4, 2Mg+SiO2,
2Nd+3AgO, 2Nd+3CuO, 2Nd+3HgO, 10Nd+3I2O5, 4Nd+3MnO2, 4Nd+3PbO2, 8Nd+3Pb3O4, 2Nd+3PdO, 4Nd+3WO2, 2Nd+WO3,
2Ta+5AgO, 2Ta+5CuO, 6Ta+5Fe2O3, 2Ta+5HgO, 2Ta+I2O5, 2Ta+5PbO, 4Ta+5PbO2, 8Ta+5Pb3O4, 2Ta+5PdO, 4Ta+5WO2, 6Ta+5WO3,
3Th+2B2O3, 3Th+2Cr2O3, Th+2CuO, 3Th+2Fe2O3, 2Th+Fe3O4, Th+MnO2, Th+PbO2, 2Th+Pb3O4, Th+SiO2,
3Ti+2B2O3, 3Ti+2Cr2O3, Ti+2CuO, 3Ti+2Fe2O3, Ti+Fe3O4, Ti+MnO2, 2Ti+Pb3O4, Ti+SiO2,
2Y+3CuO, 8Y+3Fe3O4, 10Y+3I2O5, 4Y+3MnO2, 2Y+MoO3, 2Y+Ni2O3, 4Y+3PbO2, 2Y+3PdO, 4Y+3SnO2, 10Y+3Ta2O5, 10Y+3V2O5, 2Y+WO3,
3Zr+2B2O3, 3Zr+2Cr2O3, Zr+2CuO, 3Zr+2Fe2O3, 2Zr+Fe3O4, Zr+MnO2, 2Zr+Pb3O4, Zr+SiO2, - It will be appreciated that the above descriptions are intended only to serve as examples, and that many other embodiments are possible within the scope of the present invention as defined in the appended claims.
Claims (24)
1. A method comprising the steps of
(a) providing a mixture of at least a metal oxide and a metal which undergoes an exothermic chemical reaction; and
(b) applying microwave radiation to the mixture so as to generate a localized hot spot in the mixture, said localized hot spot having at least one dimension smaller than the wavelength of the microwave radiation, thereby initiating the exothermic chemical reaction.
2. The method of claim 1 , wherein said exothermic chemical reaction has an ignition temperature in excess of 900 degrees Celsius.
3. The method of claim 1 , wherein said exothermic chemical reaction has an ignition temperature in excess of 1400 degrees Celsius.
4. The method of claim 1 , wherein said exothermic chemical reaction is a thermite reaction.
5. The method of claim 1 , wherein the microwave radiation is generated by a microwave source of power less than 2 kW.
6. The method of claim 1 , wherein the microwave radiation is generated by a microwave source of power less than 200 W.
7. The method of claim 1 , wherein the microwave radiation is generated by a solid-state microwave source.
8. The method of claim 1 , wherein the microwave radiation is generated at one or more frequency in the range of 300 MHz to 300 GHz.
9. The method of claim 1 , wherein a total mass of said mixture is less than 10 g.
10. The method of claim 1 , wherein a total mass of said mixture is less than 1 g.
11. The method of claim 1 , wherein said applying is performed by coupling an evanescent field with the mixture.
12. The method of claim 1 , wherein said applying is performed using an open ended waveguide as an applicator.
13. The method of claim 1 , wherein said applying is performed using a waveguide terminating at one or more slot as an antenna.
14. The method of claim 1 , wherein the mixture is deployed so as to achieve cutting, drilling, or welding of adjacent materials when initiated.
15. The method of claim 1 , wherein said applying is performed underwater or in another oxygen free environment.
16. The method of claim 1 , wherein the mixture includes rust formed on the surface of an iron-based metal object and a reactive metal such that the chemical reaction is effective to convert said rust to iron.
17. The method of claim 1 , wherein the mixture is dynamically added to a reaction region within which the microwave radiation is applied to the mixture during application of the microwave radiation to the mixture.
18. The method of claim 1 , wherein the mixture includes at least one gas-generating reagent.
19. The method of claim 18 , wherein said applying microwave radiation is performed within a rocket motor arrangement to generate thrust.
20. The method of claim 18 , further comprising converting gas pressure to mechanical motion so as to serve as an engine powering a mechanical device.
21. The method of claim 1 , wherein said mixture is chosen so that said exothermic reaction performs a self-propagating high-temperature synthesis (SHS) of a porous material.
22. The method of claim 1 , wherein the microwave radiation is provided to the mixture via a plurality of applicators.
23. A method comprising the steps of:
(a) providing a mixture of at least a metal oxide and a metal which undergoes an exothermic chemical reaction; and
(b) applying microwave radiation to the mixture so as to generate heat within the mixture, thereby initiating the exothermic chemical reaction, wherein said microwave radiation is applied in a manner so as to satisfy at least one of the conditions:
(i) a hot spot is generated in the mixture, said hot spot having at least one dimension smaller than the wavelength of the microwave radiation;
(ii) heat is generated in a region having at least one dimension smaller than the wavelength of the microwave radiation;
(iii) a hot spot is generated in a region smaller than a volume of the mixture.
24. A method comprising the steps of:
(a) providing a mixture of at least a metal oxide and a metal which undergoes an exothermic chemical reaction; and
(b) applying electromagnetic radiation at one or more frequency in the range of 1 MHz to 1 THz to the mixture so as to generate heat within the mixture, thereby initiating the exothermic chemical reaction, said electromagnetic radiation is applied in a manner so as to satisfy at least one of the conditions;
(i) a hot spot is generated in the mixture, said hot spot having at least one dimension smaller than the wavelength of the electromagnetic radiation;
(ii) heat is generated in a region having at least one dimension smaller than the wavelength of the electromagnetic radiation;
(iii) a hot spot is generated in a region smaller than a volume of the mixture.
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| PCT/IB2012/050964 WO2012120412A1 (en) | 2011-03-06 | 2012-03-01 | Thermite ignition and rusty iron regeneration by localized microwaves |
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| US9091517B1 (en) * | 2012-12-20 | 2015-07-28 | Los Alamos National Security, Llc | Insensitive detonator apparatus for initiating large failure diameter explosives |
| US9097503B1 (en) | 2012-12-20 | 2015-08-04 | Los Alamos National Security, Llc | Munitions having an insensitive detonator system for initiating large failure diameter explosives |
| US9341456B2 (en) * | 2014-01-21 | 2016-05-17 | Spectre Enterprises, Inc. | Self-propelled projectile having a fuel-rich propellant that reacts with water |
| US20160226531A1 (en) * | 2013-10-04 | 2016-08-04 | Johnson Matthey Public Limited Company | Data transfer apparatus |
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| US11585622B1 (en) | 2016-04-19 | 2023-02-21 | Triad National Security, Llc | Microwave ignition systems with launcher affixed to or located within a gun spindle |
| US12416094B2 (en) | 2022-01-26 | 2025-09-16 | Battelle Savannah River Alliance Llc | Localized electrorefining of metals and alloys |
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| JP2018526137A (en) * | 2015-09-03 | 2018-09-13 | エレンザ, インコーポレイテッド | Rechargeable intraocular implant |
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| US10641572B1 (en) * | 2016-04-19 | 2020-05-05 | Triad National Security, Llc | Microwave ignition of energetic material housed within a gun |
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| US12208927B2 (en) | 2019-02-28 | 2025-01-28 | Oqab Dietrich Induction Inc. | Systems and methods for controlling a target satellite |
| JP7645189B2 (en) | 2019-02-28 | 2025-03-13 | オカブ ディートリヒ インダクション インコーポレイテッド | System and method for controlling a target satellite |
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