US3032451A - Solid jet or rocket fuel - Google Patents

Solid jet or rocket fuel Download PDF

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US3032451A
US3032451A US459079A US45907954A US3032451A US 3032451 A US3032451 A US 3032451A US 459079 A US459079 A US 459079A US 45907954 A US45907954 A US 45907954A US 3032451 A US3032451 A US 3032451A
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metal
particles
fuel
dust
combustion
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US459079A
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Jr Harry A Toulmin
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Commonwealth Engineering Company of Ohio
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    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B33/00Compositions 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
    • C06B33/02Compositions 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 with an organic non-explosive or an organic non-thermic component
    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B23/00Compositions characterised by non-explosive or non-thermic constituents
    • C06B23/007Ballistic modifiers, burning rate catalysts, burning rate depressing agents, e.g. for gas generating
    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06CDETONATING OR PRIMING DEVICES; FUSES; CHEMICAL LIGHTERS; PYROPHORIC COMPOSITIONS
    • C06C15/00Pyrophoric compositions; Flints

Definitions

  • the invention is particularly useful in providing a fuel comprising for example a mixture of powdered carbonaceous material such as coal, charcoal or the like and powdered metals which are of relatively low molecular weight and burn easily and quickly to produce high temperatures and high velocity gases.
  • a still further object of the invention is to provide a method for accelerating the combustion of powdered combustible substances whereby the flame spreads through the mass of fuel and brings about the exploding and rapid disintegration of each of the powdered particles and the propagation of high velocity combustion gases.
  • the powdered fuel mixture of the invention is characterized by exhibiting a high flame speed during combustion and the production of a high pressure area.
  • a basic process is provided for obtaining high temperatures of combustion and the production of high exhaust velocity gases for propulsion purposes.
  • the invention will be described more particularly with reference to the use of mixtures of powdered coals and powdered metals, e.g., aluminum and magnesium, however, other combustible powdered carbon and metals of similar nature may be used or admixed therewith to provide an improved fuel.
  • metals of low atomic weight for example aluminum, magnesium, beryllium
  • a catalysts such as a metallic soap.
  • the particle size of the metal is generally on the order of 20 microns or less and preferably a micron or less in diameter.
  • the particle size of the coal or carbonaceous material is generally less than 1000 microns and preferably substantially in the same particle size range as the metal powder.
  • the mixture of coal dust, metal dust and metallic soap may be used as a dry powder fuel or admixed with liquid hydrocarbon to form a slurry.
  • the proportionate amount of coal or charcoal dust and atent 3,032,451 Patented May I, 1962 metal powder employed may, of course, be varied depending upon the metal powder used as well as the kind of coal dust employed and the particular use to which the fuel is to be put.
  • the amount of powdered metal present may range between about 1% and 35% by weight of the powdered mixture of coal dust and metal powder. Since the cost of powdered metal is relatively high as compared to powdered coal, the metal powder is used more sparingly.
  • a metallic soap or mixture of such metallic soaps for example 0.1 to 5% by weight of the powdered metal constituents comprises a metallic soap such as a stearate, palmitate, oleate, ricinoleate, etc., of aluminum, magnesium, beryllium, titanium, zirconium, tin or the like which exhibit auto oxidation catalytic properties.
  • the metal particles of the fuel mixture are in the form of dust or flakes, with metallic soap being preferably coated on or admixed with the flakes of metal, e.g., aluminum metal flakes coated with aluminum stearate mixed with coal dust forms an excellent fuel mixture.
  • the carbonaceous and metal particles in the form of flakes or dust and metallic soap catalyst are dispersed in a liquid hydrocarbon, for example kerosene, gasoline, diesel oil, etc., to provide a liquid combustible carrier for the powdered metalmaterials.
  • a liquid hydrocarbon for example kerosene, gasoline, diesel oil, etc.
  • Such a fuel is useful for operating jet engines, rockets and high temperature operated prime movers, and where the maximum B.t.u.s are to be extracted from the burning fuel in a predetermined time.
  • a peroxide such as hydrogen or benzyl peroxide, etc. may be introduced into the fuel mixture initially or during the burning of the same.
  • 0.5 to 2% by weight of the fuel solids may comprise a peroxide.
  • the improved powdered metal fuel of this invention a mixture of powdered coal, aluminum metal dust, preferably as powdered metal foil of a particle fineness of an average size of one micron is coated with aluminum stearate (0.1 to 5% by weight of the powdered metal mixture).
  • aluminum metal other low atomic weight metals such as beryllium and magnesium, or suitable mixtures thereof may be used.
  • Small amounts up to 1% of other combustible metals, e.g., titanium metal powder, zirconium, zinc or tin may be present.
  • the metallic soap utilized as auto oxidation catalysts are preferably salts of metals in groups II, III and IV of the periodic table, representatives of which are the stearates or palmitates of aluminum, magnesium, titanium, zirconium and tin.
  • the powdered fuel mixture of coal dust and metal powder may be used in the form of a slurry, the same being admixed with liquid hydrocarbon and discharged into a combustion chamber.
  • This slurry of oil and dust particles may be sprayed into a combustion chamber of the engine and mixed with air or oxygen, preferably as liquid ozone, and burned.
  • air or oxygen preferably as liquid ozone
  • one to twenty-five parts of the solid fuel constituents to parts by weight of the liquid hydrocarbon provides a suitable liquid fuel mixture.
  • Liquid ozone in amount of 0.1 to 1% by weight of the total fuel mixture may be used.
  • the burning of the fuel with ozone increases the exhaust velocity substantially over the use of air or oxygen alone. Higher or lower proportionate amounts of the liquid hydrocarbon and powdered fuel constituents may be employed as needed, to provide a fuel having the requisite consistency and burning characteristics desired.
  • the powdered fuel may be mixed with the liquid hydrocarbon either before or during burning of the mixture.
  • the presence of the auto-oxidation catalyst in suflicient amount to catalyze the reaction forms an essential con stituent of the powdered fuel.
  • the metal particles which are combustible and tend to vaporize readily produce a high temperature reaction during the combustion.
  • Powdered aluminum metal for example, produces a flame having a temperature of 3500 C. or higher.
  • the very high temperatures produced during the catalyzed reaction causes the powdered coal and metal particles to be rapidly disintegrated and vaporized.
  • the combustion of the metal and coal particles thus proceed at a high rate, the temperature and explosive action being enhanced by the catalytic action of the metallic soap.
  • the high temperatures produced combined with the violent disintegration and vaporization of the powdered fuel particles is believed to account for the unexpected high calorific values produced.
  • the catalytic action of metallic soaps facilitates the burning of the metal dust and provides a high temperature reaction so that the'maximum B.t.u.s are obtained from the solid fuel particles.
  • the high temperatures produced rapidly transform the metal particles into gases at high temperatures.
  • pyrophoric metal powders for example of aluminum, magnesium and beryllium together with coal dust
  • a petroleum hydrocarbon carrier such as gasoline, kerosene, diesel oil or the like
  • gasoline, kerosene, diesel oil or the like provides a fuel which is more sensitive to ignition and a fuel mixture wherein the flame produced by combustion proceeds more rapidly through the fuel, than when the dust particles are employed alone.
  • the high temperature gases formed by the combustion of the mixture results in the production of high velocity exhaust gases.
  • an excess of oxygen in the atmosphere is preferred and is introduced into the fuel either from a liquid ozone or mixture of air and peroxide, as heretofore explained. In this manner it is possible to produce the combustion at a lower ignition temperature and increase the rate of combustion and the adsorption of oxygen on the dust particles.
  • Metal particles such as aluminum, magnesium, beryllium and the like combustible material in the form of dust ignited in the presence of metallic soap catalytic agent burns at a high rate and temperature.
  • the combustion rate promoting catalysts produce a powdered metal fuel which has a lower explosive limit or temperature, particularly in the presence of methane, oxygen or air, and results in the enhancement of the combustion of the fuel.
  • Control of the combustion and explosive properties of the powdered fuel mixture can be effected by utilizing different oxidizing agents and in various proportions.
  • the incendiary action of the fuel may be controlled so as to either accelerate the combustion or burning up of the fuel particles or slow down their combustion as may be required in the use of the fuel.
  • the combustion may be speeded up by the use of metallic soap and peroxide catalysts so that the mixture will burn and provide the high temperature reaction gases necessary to propel the piston in a predetermined time.
  • the use of negative catalysts such as those which do not accelerate the combustion but tend to decelerate the combustion are incorporated in the fuel.
  • the ignition of the same is believed to have an electric or electronic origin as opposed to thermal ignition.
  • the electrical discharges or ionization is believed to produce ozone and aluminum oxide (A1 0 which reacts with the fine dust particles and initiates the decomposition of the same and flame propagation during the combustion of the fuel.
  • the electrical ignition depends largely upon the production of a sufiicient concentration of charged particles and which results from electronic collisions due to ionization of the materials or the presence of ions or ionzed particles in the explosive-mixture. This electronic phase of the combustion is believed to play an important roll in the increased efiiciency of the fuel of this invention. The same is substantially true in the case of thermal ignition.
  • the concentration such as will provide sufficient heat to produce complete oxidization of the combustible coal and metal dust particles and thus release the maximum B.t.u.s.
  • the heat produced by complete oxidization of a portion of the dust particles in the available oxygen is enough to heat the rest of the dust in the mixture to bring the same to the ignition temperature.
  • the strongest explosion or greatest explosive force should be produced at a concentration corresponding to stoichiometric weight mixtures of the fuel ingredients. This can be computed if the chemical composition of the dust is known and provided complete combustion of the material is assumed to take place. In practice, however, somewhat richer dust mixtures are found to be the most explosive.
  • a flame or hot surface As a source of ignition it is preferred to utilize a flame or hot surface.
  • moisture which normally is a constituent of the mixture is advantageous since it reacts with the metal powder and similar mate rials at the reaction temperatures and results in the evolution of hydrogen gas.
  • the production of hydrogen gas is effected particularly at elevated temperatures wherein decomposition and ionization of moisture is produced. This reduces the surface oxide coating which would otherwise tend to form on the particles and thus makes the fuel mixture highly sensitive to ignition and combustion.
  • pyrophoric metal dust particles may be present such as finely divided metal powders of iron, manganese, copper, uranium, nickel, zirconium and others, metal oxides, hydrides, carbid3s, nitrides and metal alloys which also oxidize rapidly on exposure to air that they tend to heat and ignite. While there is no apparent agreement regarding the exact mechanism of the pyrophoric ignition, it is believed that the process varies somewhat with the type of dust, its fineness and surface character.
  • the basic discovery in this invention is that by utilizing a combination of combustible metal dust with coal dust that the combustion can be achieved and controlled whereby the maximum liberation of gas and heat results from the reaction.
  • the pyrophoricity of these dusts is believed to be relaed to a metastable internal equilibrium in the powders.
  • one of the advantages of utilizing these dusts of pyrophoric character, such as aluminum and/or magnesium or beryllium metal dusts is that with a sufiicient dispersion of these extremely fine particles, the same will self-ignite by an electrostatic spark discharge within the cloud of dust.
  • the igniting energy of these dust clouds may vary with the fineness, the moisture content and somewhat with the concentration in the cloud. For instance, undispersed layers of beryllium metal powder have been ignited by sparks of less than 1 microjoule (1 muj.) energy while other dusts take considerably stronger sparks.
  • the igniting energy of dust clouds in air ranges from about 10 millijoules (10 mi.) to several joules.
  • the igniting source generally preferred is a high voltage induction spark.
  • a high voltage induction spark When these dusts are thus ignited the pressure is developed to more than 1b./in. and rises to an average rate of pressure of about 5000 lb./in. per second and the maximum rates to more than 10,000 lb./in. per second.
  • a satisfactory result can be secured.
  • the minimum concentration of coal dust that will propagage large-scale explosions is approximately 50 mg./liter (0.05 oz./ft. of air. Pressure is nearly 150 lb./in. and flame velocities in excess of 6-000 ft./sec. have been accomplished by the employment of the thermal properties of the metal dust and the catalysts, e.g., aluminum flakes and similar other dusts.
  • the thermal properties of the metal dust and the catalysts e.g., aluminum flakes and similar other dusts.
  • the present invention provides a novel fuel and method of producing high temperature combustion reactions, and wherein metal dust particles form a principal constituent.
  • the invention provides a fuel wherein a catalyzed metal dust is utilized to produce a high temperature fuel and wherein the maximum B.t.u. values are obtained.
  • a fuel mixture consisting essentially of particles of coal, particles of metal and a catalys for promoting the burning of the fuel mixture, the particles of coal constituting the principal constituent and said metal particles constituting from 1% to 35% by weight of the mixture of coal and metal particles, said metal particles being selected from the group consisting of aluminum, magnesium and beryllium, said catalyst consisting of a fatty acid salt of a metal selected from the group consisting of aluminum, magnesium, titanium, zirconium and tin, and said fatty acid metal salt constituting from 0.1% to 5% by weight of the metal particles and the balance of the fuel mixture being composed of particles of coal.
  • a fuel mixture consisting essentially of the combination of powdered solid constituents and a catalyst for promoting the burning of the fuel mixture, said solids consisting essentially of particles of coal which constitutes the principal constituent, particles of metal and a catalyst consisting of fatty acid salt of a metal selected from the group consisting of aluminum, magnesium, titanium, zirconium and tin, said metal particles constituting from 1%to 35% by weight of the mixture of coal and metal particles, and said catalyst consisting.
  • a fuel mixture consisting essentially of particles of coal which constitutes the principal constituent, particles of metal and a catalyst for promoting the burning of the fuel mixture, said metal particles consisting of aluminum metal and which is present in an amount between about 1% and 35% by weight of the mixture of coal particles and metal particles, and aluminum stearate t catalyze the burning of the fuel mixture, and said catalyst consisting of 0.1% to 5% by weight of said metal particles of the fuel mixture and the balance of the fuel mixture being composed of particles of coal.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Metallurgy (AREA)
  • Materials Engineering (AREA)
  • Solid Fuels And Fuel-Associated Substances (AREA)
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Description

United States The invention is particularly useful in providing a fuel comprising for example a mixture of powdered carbonaceous material such as coal, charcoal or the like and powdered metals which are of relatively low molecular weight and burn easily and quickly to produce high temperatures and high velocity gases.
It is a principal objectof the invention to provide a catalyzed powdered mixture which forms a suitable fuel for jet airplane engines, gas turbines, rockets, missiles, propellants, power plants, and as utilized in the fields of aviation, rail transportation, agricultural distribution systems for fertilizer and insecticides, destruction of vegetation, and as may be useful for military purposes, as for example flame throwers, fire bombs, etc.
It is another object of the invention to provide a composition useful as feul, explosive products or as ignition catalysts for initiating and promoting high temperature reactions and the production of high velocity hot gases.
It is another object of the invention to provide a combustible composition which has very short flame propulsion area and which exhibits an accelerated rate of combustion due to the highly pyrophoric character of the fuel mixture.
It is another object of the invention to provide a powdered fuel mixture which may be used in the form of a slurryand containing auto-oxidation catalyst dispersed in a liquid hydrocarbon, and which produces a large amount of exothermic heat during combustion.
A still further object of the invention is to provide a method for accelerating the combustion of powdered combustible substances whereby the flame spreads through the mass of fuel and brings about the exploding and rapid disintegration of each of the powdered particles and the propagation of high velocity combustion gases. The powdered fuel mixture of the invention is characterized by exhibiting a high flame speed during combustion and the production of a high pressure area. By utilizing a suitable mixture of coal dust, metal dust, and auto oxidation catalysts, and dispersing the same while introducing a sufl'icient supply of air or oxygen, and preferably in the form of liquid ozone, maximum evolution of heat is obtained during combustion of the dust.
In accordance with the invention, a basic process is provided for obtaining high temperatures of combustion and the production of high exhaust velocity gases for propulsion purposes. The invention will be described more particularly with reference to the use of mixtures of powdered coals and powdered metals, e.g., aluminum and magnesium, however, other combustible powdered carbon and metals of similar nature may be used or admixed therewith to provide an improved fuel.
In preparing the fuel mixture powdered metal material, especially metals of low atomic weight, for example aluminum, magnesium, beryllium, are mixed with powdered coal or carbonaceous material and a catalysts such as a metallic soap. The particle size of the metal is generally on the order of 20 microns or less and preferably a micron or less in diameter. The particle size of the coal or carbonaceous material is generally less than 1000 microns and preferably substantially in the same particle size range as the metal powder. The mixture of coal dust, metal dust and metallic soap may be used as a dry powder fuel or admixed with liquid hydrocarbon to form a slurry.
The proportionate amount of coal or charcoal dust and atent 3,032,451 Patented May I, 1962 metal powder employed may, of course, be varied depending upon the metal powder used as well as the kind of coal dust employed and the particular use to which the fuel is to be put. For most purposes, the amount of powdered metal present may range between about 1% and 35% by weight of the powdered mixture of coal dust and metal powder. Since the cost of powdered metal is relatively high as compared to powdered coal, the metal powder is used more sparingly.
To catalyze and enhance the combustion rate of the powdered fuel mixture and produce a high temperature reaction, there is introduced a small amount of a metallic soap or mixture of such metallic soaps, for example 0.1 to 5% by weight of the powdered metal constituents comprises a metallic soap such as a stearate, palmitate, oleate, ricinoleate, etc., of aluminum, magnesium, beryllium, titanium, zirconium, tin or the like which exhibit auto oxidation catalytic properties. The metal particles of the fuel mixture are in the form of dust or flakes, with metallic soap being preferably coated on or admixed with the flakes of metal, e.g., aluminum metal flakes coated with aluminum stearate mixed with coal dust forms an excellent fuel mixture.
Where the fuel is to be employed as a liquid, the carbonaceous and metal particles in the form of flakes or dust and metallic soap catalyst are dispersed in a liquid hydrocarbon, for example kerosene, gasoline, diesel oil, etc., to provide a liquid combustible carrier for the powdered metalmaterials. Such a fuel is useful for operating jet engines, rockets and high temperature operated prime movers, and where the maximum B.t.u.s are to be extracted from the burning fuel in a predetermined time.
For promoting the oxidation and increasing the speed of burning of the fuel, a peroxide such as hydrogen or benzyl peroxide, etc. may be introduced into the fuel mixture initially or during the burning of the same. For this purpose 0.5 to 2% by weight of the fuel solids may comprise a peroxide.
As specific examples of the improved powdered metal fuel of this invention a mixture of powdered coal, aluminum metal dust, preferably as powdered metal foil of a particle fineness of an average size of one micron is coated with aluminum stearate (0.1 to 5% by weight of the powdered metal mixture). In place of aluminum metal other low atomic weight metals such as beryllium and magnesium, or suitable mixtures thereof may be used. Small amounts up to 1% of other combustible metals, e.g., titanium metal powder, zirconium, zinc or tin may be present.
The metallic soap utilized as auto oxidation catalysts are preferably salts of metals in groups II, III and IV of the periodic table, representatives of which are the stearates or palmitates of aluminum, magnesium, titanium, zirconium and tin.
The powdered fuel mixture of coal dust and metal powder may be used in the form of a slurry, the same being admixed with liquid hydrocarbon and discharged into a combustion chamber. This slurry of oil and dust particles may be sprayed into a combustion chamber of the engine and mixed with air or oxygen, preferably as liquid ozone, and burned. In generaly', one to twenty-five parts of the solid fuel constituents to parts by weight of the liquid hydrocarbon provides a suitable liquid fuel mixture. Liquid ozone in amount of 0.1 to 1% by weight of the total fuel mixture may be used. The burning of the fuel with ozone increases the exhaust velocity substantially over the use of air or oxygen alone. Higher or lower proportionate amounts of the liquid hydrocarbon and powdered fuel constituents may be employed as needed, to provide a fuel having the requisite consistency and burning characteristics desired. The powdered fuel may be mixed with the liquid hydrocarbon either before or during burning of the mixture.
The presence of the auto-oxidation catalyst in suflicient amount to catalyze the reaction forms an essential con stituent of the powdered fuel. The metal particles which are combustible and tend to vaporize readily produce a high temperature reaction during the combustion. Powdered aluminum metal, for example, produces a flame having a temperature of 3500 C. or higher. The very high temperatures produced during the catalyzed reaction causes the powdered coal and metal particles to be rapidly disintegrated and vaporized. The combustion of the metal and coal particles thus proceed at a high rate, the temperature and explosive action being enhanced by the catalytic action of the metallic soap. The high temperatures produced combined with the violent disintegration and vaporization of the powdered fuel particles is believed to account for the unexpected high calorific values produced.
Heretofore, in the combustion of solid fuel particles, the maximum B.t.u.s have not been obtained principally because the initial heating of the particles did not result in the production of temperatures high enough to disintegrate and vaporize the particles and permit air or oxygen to come in contact with all the particles and support its combustion to completion. In other words, under conventional combustion reactions using powdered metals there was always a certain minimum amount of the particles which were not burned to completion but passed off as smoke.
By utilizing a mixture of powdered metal, powdered coal or the like carbonaceous material and auto oxidation catalyst admixed with oxygen and burned in the combustion chamber, there is produced high temperature and high velocity gases for operating the jet engine. The proportionate amount of fuel used is controlled so as to produce the most eflicient operation of the engine.
The production of high temperatures during the combustion results in the maximum extraction of B.t.u.s from the powdered coal and powdered metal material. To achieve this, however, it is requisite that the reaction be conducted so that the boiling point or vaporization point of the combustible material is lower than the flame temperature, and that the heat of vaporization is lower than the energy required to initiate rapid surface oxidation or combustion.
The catalytic action of metallic soaps facilitates the burning of the metal dust and provides a high temperature reaction so that the'maximum B.t.u.s are obtained from the solid fuel particles. During combustion of the fuel the high temperatures produced rapidly transform the metal particles into gases at high temperatures.
Further, the use of pyrophoric metal powders, for example of aluminum, magnesium and beryllium together with coal dust, when used with a petroleum hydrocarbon carrier such as gasoline, kerosene, diesel oil or the like provides a fuel which is more sensitive to ignition and a fuel mixture wherein the flame produced by combustion proceeds more rapidly through the fuel, than when the dust particles are employed alone. y Moreover, the high temperature gases formed by the combustion of the mixture results in the production of high velocity exhaust gases.
In addition to the high'rate' of'rea'ction and production of high temperatures and high gas velocities during combustion of metal dust and coal particles, it has been found that the addition of a small amount of a metallic soap such'as aforementioned, for example aluminum, magnesium stearate or oleate or the like, will further accelerate this ignition and flame propagation during combustion of the fuel. This is probably due'to the fact that the porous surface of the particles adsorb gas from the surrounding atmosphere and the metallic soap catalyzes the reaction.
To control the combustion and prevent explosion and to facilitate combustion an excess of oxygen in the atmosphere is preferred and is introduced into the fuel either from a liquid ozone or mixture of air and peroxide, as heretofore explained. In this manner it is possible to produce the combustion at a lower ignition temperature and increase the rate of combustion and the adsorption of oxygen on the dust particles.
Metal particles such as aluminum, magnesium, beryllium and the like combustible material in the form of dust ignited in the presence of metallic soap catalytic agent burns at a high rate and temperature. The combustion rate promoting catalysts produce a powdered metal fuel which has a lower explosive limit or temperature, particularly in the presence of methane, oxygen or air, and results in the enhancement of the combustion of the fuel.
Control of the combustion and explosive properties of the powdered fuel mixture can be effected by utilizing different oxidizing agents and in various proportions. In this manner the incendiary action of the fuel may be controlled so as to either accelerate the combustion or burning up of the fuel particles or slow down their combustion as may be required in the use of the fuel. Thus, for making a fuel useful in internal combustion engines utilizing powdered carbon such as coal dust and metal powder, the combustion may be speeded up by the use of metallic soap and peroxide catalysts so that the mixture will burn and provide the high temperature reaction gases necessary to propel the piston in a predetermined time. In other instances where the fuel is required to burn more slowly, the use of negative catalysts such as those which do not accelerate the combustion but tend to decelerate the combustion are incorporated in the fuel.
In the case of metal dust such as aluminum dust and similar metal dust, the ignition of the same is believed to have an electric or electronic origin as opposed to thermal ignition. The electrical discharges or ionization is believed to produce ozone and aluminum oxide (A1 0 which reacts with the fine dust particles and initiates the decomposition of the same and flame propagation during the combustion of the fuel.
The electrical ignition depends largely upon the production of a sufiicient concentration of charged particles and which results from electronic collisions due to ionization of the materials or the presence of ions or ionzed particles in the explosive-mixture. This electronic phase of the combustion is believed to play an important roll in the increased efiiciency of the fuel of this invention. The same is substantially true in the case of thermal ignition.
It is also considered to be immaterial whether the theory of predistillation of dust during ignition and combustion takes place or whether such a theory may be used to explain what happens to the fuel during combustion, or whether it involves some other theory for the production of the improved results. In the case of the predistillation theory of dust ignition, it is believed that all dust ignition involves purely a gas or vapor explosion and that the energy of the ignition source provides heat to decompose the dust particles thus causing the evolution of the volatile matter. In this manner-the volatilized gassy particles mix more readily with air and ignite and the combustion proceeds at a high rate and the heat produced in turn further heats and volatilizes other particles not yet volatilized.
One of the objections made to the above theory has been that the ignition temperature of some dust, including' coal, are lower than the ignition temperatures of the gases involved such as methane or the like hydrocarbon. However, there seems to be some support for the theory that during the initial heating and combustion of the dust there is not enough air present at thc'surface of the particle to continue to support the combustion, and
consequently the temperature rises above the ignition point of the solid causing it to distill and eventually to ignite, thus initiating the combustion reaction.
In the preferred process of carrying out of the combustion of the novel fuel of this invention, it is sought to have the concentration such as will provide sufficient heat to produce complete oxidization of the combustible coal and metal dust particles and thus release the maximum B.t.u.s. The heat produced by complete oxidization of a portion of the dust particles in the available oxygen is enough to heat the rest of the dust in the mixture to bring the same to the ignition temperature. Theoretically, neglecting disassociation, the strongest explosion or greatest explosive force should be produced at a concentration corresponding to stoichiometric weight mixtures of the fuel ingredients. This can be computed if the chemical composition of the dust is known and provided complete combustion of the material is assumed to take place. In practice, however, somewhat richer dust mixtures are found to be the most explosive.
The adjustment of these mixtures to provide the greatest heat production is facilitated by the catalytic action of the metal powder constituent together with the auto-oxidation catalyst, and the fluid carrier which is preferably hydrocarbon as described. The initial temperature, pressure, oxygen, content, humidity, specific heat and heat conductivity of the atmosphere all are factors which influence the dust explosion. The presence of oxygen is, of course, a most important factor.
As a source of ignition it is preferred to utilize a flame or hot surface. The presence of moisture which normally is a constituent of the mixture is advantageous since it reacts with the metal powder and similar mate rials at the reaction temperatures and results in the evolution of hydrogen gas. The production of hydrogen gas is effected particularly at elevated temperatures wherein decomposition and ionization of moisture is produced. This reduces the surface oxide coating which would otherwise tend to form on the particles and thus makes the fuel mixture highly sensitive to ignition and combustion.
Other pyrophoric metal dust particles may be present such as finely divided metal powders of iron, manganese, copper, uranium, nickel, zirconium and others, metal oxides, hydrides, carbid3s, nitrides and metal alloys which also oxidize rapidly on exposure to air that they tend to heat and ignite. While there is no apparent agreement regarding the exact mechanism of the pyrophoric ignition, it is believed that the process varies somewhat with the type of dust, its fineness and surface character.
The basic discovery in this invention is that by utilizing a combination of combustible metal dust with coal dust that the combustion can be achieved and controlled whereby the maximum liberation of gas and heat results from the reaction. The pyrophoricity of these dusts, as hereinbefore mentioned, is believed to be relaed to a metastable internal equilibrium in the powders. Thus, one of the advantages of utilizing these dusts of pyrophoric character, such as aluminum and/or magnesium or beryllium metal dusts, is that with a sufiicient dispersion of these extremely fine particles, the same will self-ignite by an electrostatic spark discharge within the cloud of dust.
Particularly satisfactory results have been secured with dust samples of finer than ZOO-mesh. This fuel can be passed through an electrically heated cylindrical alundumcore furnace construction for ignition. The ignition temperatures for the dust will range from about 200 C. to more than 1000 C. These figures depend upon the dispzrsibility, fineness, uniformity of the dust, the ignition source, the timing of ignition and the interpretation,
of what constitutes limiting flame propagation.
The igniting energy of these dust clouds may vary with the fineness, the moisture content and somewhat with the concentration in the cloud. For instance, undispersed layers of beryllium metal powder have been ignited by sparks of less than 1 microjoule (1 muj.) energy while other dusts take considerably stronger sparks. The igniting energy of dust clouds in air ranges from about 10 millijoules (10 mi.) to several joules.
The igniting source generally preferred is a high voltage induction spark. When these dusts are thus ignited the pressure is developed to more than 1b./in. and rises to an average rate of pressure of about 5000 lb./in. per second and the maximum rates to more than 10,000 lb./in. per second. When using a high voltage continuous induction spark and dispersing the dust through a furnace at 850 C. a satisfactory result can be secured.
The minimum concentration of coal dust that will propagage large-scale explosions is approximately 50 mg./liter (0.05 oz./ft. of air. Pressure is nearly 150 lb./in. and flame velocities in excess of 6-000 ft./sec. have been accomplished by the employment of the thermal properties of the metal dust and the catalysts, e.g., aluminum flakes and similar other dusts. As hereinbefore stated, in the presence of a liquid hydrocarbon fuel and oxygen, it is possible to achieve temperature and gas velocities of great magnitude and by adjusting the fineness of the materials involved, the amount of moisture present and the oxygen, the maximum energy can be released.
It will thus be seen that the present invention provides a novel fuel and method of producing high temperature combustion reactions, and wherein metal dust particles form a principal constituent.
Further, the invention provides a fuel wherein a catalyzed metal dust is utilized to produce a high temperature fuel and wherein the maximum B.t.u. values are obtained.
It is understood that various changes and additions may be made in compounding the fuel of this invenion and that the proportionate amount of ingredients may be varied over a relatively wide range, depending upon the particular use to which the fuel is to be put. Such changes and variations are con emplated to come within the spirit and scope of this invention, and which are more particulary s t forth in the append:d claims.
What is claimed is:
1. A fuel mixture consisting essentially of particles of coal, particles of metal and a catalys for promoting the burning of the fuel mixture, the particles of coal constituting the principal constituent and said metal particles constituting from 1% to 35% by weight of the mixture of coal and metal particles, said metal particles being selected from the group consisting of aluminum, magnesium and beryllium, said catalyst consisting of a fatty acid salt of a metal selected from the group consisting of aluminum, magnesium, titanium, zirconium and tin, and said fatty acid metal salt constituting from 0.1% to 5% by weight of the metal particles and the balance of the fuel mixture being composed of particles of coal.
2. A fuel mixture consisting essentially of the combination of powdered solid constituents and a catalyst for promoting the burning of the fuel mixture, said solids consisting essentially of particles of coal which constitutes the principal constituent, particles of metal and a catalyst consisting of fatty acid salt of a metal selected from the group consisting of aluminum, magnesium, titanium, zirconium and tin, said metal particles constituting from 1%to 35% by weight of the mixture of coal and metal particles, and said catalyst consisting.
of 0.1% to 5% by weight of said metal particles of the fuel mixture and the balance of the fuel mixture being composed of particles of coal.
3. A fuel mixture consisting essentially of particles of coal which constitutes the principal constituent, particles of metal and a catalyst for promoting the burning of the fuel mixture, said metal particles consisting of aluminum metal and which is present in an amount between about 1% and 35% by weight of the mixture of coal particles and metal particles, and aluminum stearate t catalyze the burning of the fuel mixture, and said catalyst consisting of 0.1% to 5% by weight of said metal particles of the fuel mixture and the balance of the fuel mixture being composed of particles of coal.
References Cited in the file of this patent UNITED STATES PATENTS ONeil Aug. 26, 1924 Pearsall Feb. 25, 1947 Van Loenen Nov. 21, 1950 Bartleson et a1. July 17, 1951 Clay et al. Nov. 13, 1951

Claims (1)

1. A FUEL MIXTURE CONSISTING ESSENTIALLY OF PARTICLES OF COAL, PARTICLES OF METAL AND A CATALYST: FOR PROMOTING THE BURNING OF THE FUEL MIXTURE, THE PARTICLES OF COAL CONSTITUTING THE PRINCIPAL CONSTITUENT AND SAID METAL PARTICLES CONSTITUTING FRROM 1% TO 35% BY WEIGHT OF THE MIXTURE OF COAL AND METAL PARTICLES, SAID METAL PARTICLES BEING SELECTED FROM THE GROUP CONSISTING OF ALUMINUM, MAGNESIUM AND BERYLLIUM, SAID CATALYST CONSISTING OF A FATTY ACID SALT OF A METAL SELECTED FROM THE GROUP CONSISTING OF ALUMINUM, MAGNESIUM, TITANIUM, ZIRCONIUM AND TIN, AND SAID FATTY ACID METAL SALT CONSTITUTING FROM 0.1% TO 5% BY WEIGHT OF THE METAL PARTICLES AND THE BALANCE OF THE FUEL MIXTURE BEING COMPOSED OF PARTICLES OF COAL.
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3193420A (en) * 1961-08-25 1965-07-06 Ohio Commw Eng Co Catalyzed metal fuel containing a peroxide
US3203843A (en) * 1962-01-24 1965-08-31 Hi Shear Corp Charge material
US3249474A (en) * 1964-08-03 1966-05-03 Robert B Clay Explosive composition containing inorganic salts and coated metal
US4402705A (en) * 1980-10-31 1983-09-06 Werkzeugmaschinenfabrik Oerlikon-Buhrle Ag Incendiary composition containing a group IVB metallic fuel

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1506323A (en) * 1919-12-05 1924-08-26 O'neill John Hugh Method and means of producing heat
US2416639A (en) * 1944-07-08 1947-02-25 Ensign Bickford Co Slow-burning powder composition
US2530492A (en) * 1944-09-25 1950-11-21 Kaiser Aluminium Chem Corp Method of making incendiary compositions
US2560542A (en) * 1947-06-07 1951-07-17 Standard Oil Co Clean-burning carbonaceous compositions
US2574466A (en) * 1944-11-07 1951-11-13 John P Clay Smoke agent

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1506323A (en) * 1919-12-05 1924-08-26 O'neill John Hugh Method and means of producing heat
US2416639A (en) * 1944-07-08 1947-02-25 Ensign Bickford Co Slow-burning powder composition
US2530492A (en) * 1944-09-25 1950-11-21 Kaiser Aluminium Chem Corp Method of making incendiary compositions
US2574466A (en) * 1944-11-07 1951-11-13 John P Clay Smoke agent
US2560542A (en) * 1947-06-07 1951-07-17 Standard Oil Co Clean-burning carbonaceous compositions

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3193420A (en) * 1961-08-25 1965-07-06 Ohio Commw Eng Co Catalyzed metal fuel containing a peroxide
US3203843A (en) * 1962-01-24 1965-08-31 Hi Shear Corp Charge material
US3249474A (en) * 1964-08-03 1966-05-03 Robert B Clay Explosive composition containing inorganic salts and coated metal
US4402705A (en) * 1980-10-31 1983-09-06 Werkzeugmaschinenfabrik Oerlikon-Buhrle Ag Incendiary composition containing a group IVB metallic fuel

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