Substance activation raw material and substance activation member

Abstract

The invention provides a material activation raw material and a material activation member capable of exerting a greater material activation effect. The substance activation raw material comprises: a powder of a natural mineral containing a radioactive substance; and a powder of an electron-generating substance that generates electrons using the alpha rays released from the natural mineral.

Description

Technical Field

[0001] The present invention relates to a material activation raw material and a material activation component. Background Art

[0002] In recent years, there has been proposed, for example, activation of substances such as combustion air inhaled by an engine and combustion exhaust gas discharged from the engine to reduce fuel consumption during high-speed driving and to reduce the amount of carbon dioxide contained in the exhaust gas (for example, Patent Document 1).

[0003] The radiation generated by such a material activation component ionizes substances such as combustion air and combustion exhaust gas that are the objects of activation. The charges generated during this ionization cause the metal layer constituting the metal layer to be charged, generating an electric field and a magnetic field, and this electric field and magnetic field activate the target substance, thereby enabling improvement of combustion efficiency and efficient purification of exhaust gas. Prior Art Documents Patent Documents

[0004] Patent Document 1: Japanese Patent Laid-Open Publication No. 2018-59909 Summary of the Invention Problems to be Solved by the Invention

[0005] Although conventional material activation components exhibit certain excellent effects, there is a desire for the development of new material activation raw materials and material activation components that can further enhance the activation effect of substances.

[0006] The present invention has been completed to solve such problems, and an object thereof is to provide a material activation raw material and a material activation component that can exhibit a greater activation effect of substances. Means for Solving the Problems

[0007] The above object of the present invention is achieved by a material activation raw material, which includes: a powder of a natural mineral containing a radioactive substance; and a powder of an electron generating substance that generates electrons by using alpha rays released from the natural mineral.

[0008] Furthermore, regarding the above material activation raw material, preferably, the powder of the electron generating substance includes: a powder of titanium dioxide; and a powder of at least one selected from lanthanum hexaboride, black silica, metallic magnesium, tungsten, metallic silicon, molybdenum disulfide, and germanium metal.

[0009] Furthermore, preferably, the average particle size of the powder of the natural mineral is 200 μm or less, and the average particle size of the powder of the electron generating substance is 200 μm or less.

[0010] In addition, preferably, the substance activation raw material further contains a conductive fluid binder. Additionally, the fluid binder can be non-drying or dry.

[0011] In addition, preferably, the fluid binder contains at least one powder selected from zinc, molybdenum disulfide, and copper.

[0012] In addition, the object of the present invention is achieved by a substance activation component, which includes: an electron generation part, including: a powder of natural mineral containing a radioactive substance; and a powder of an electron generation substance that generates electrons by using the alpha rays released from the natural mineral; and an electrode part connected to the electron generation part.

[0013] Regarding this substance activation component, preferably, the powder of the electron generation substance includes: a powder of titanium dioxide; and at least one powder selected from lanthanum hexaboride, black silicon dioxide, metallic magnesium, tungsten, metallic silicon, molybdenum disulfide, and germanium metal.

[0014] In addition, preferably, the average particle size of the powder of the natural mineral is 200 μm or less, and the average particle size of the powder of the electron generation substance is 200 μm or less.

[0015] In addition, the object of the present invention is achieved by a substance activation component, which includes: a substance activation raw material, including: a powder of natural mineral containing a radioactive substance; and a powder of an electron generation substance that generates electrons by using the alpha rays released from the natural mineral; and a cylindrical magnet with one end being the N pole and the other end being the S pole, and the substance activation component is formed by filling the substance activation raw material inside the cylindrical magnet. Preferably, the powder of the electron generation substance includes: a powder of titanium dioxide; and at least one powder selected from lanthanum hexaboride, black silicon dioxide, metallic magnesium, tungsten, metallic silicon, molybdenum disulfide, and germanium metal.

[0016] Regarding this substance activation component, preferably, an electrode is connected to the end on the N - pole side of the cylindrical magnet.

[0017] In addition, preferably, the electrode is a plate - shaped electrode connected to the entire area of the end face of the magnet. In addition, preferably, the plate - shaped electrode is formed to have an area larger than the area surrounded by the outer peripheral contour line of one end of the magnet. Advantages of the Invention

[0018] According to the present invention, it is possible to provide a substance activation component that can achieve a greater activation effect on substances. Brief Description of the Drawings

[0019] Figure 1 Schematic cross-sectional view of the substance activation component according to an embodiment of the present invention. Figure 2 It is related to Figure 1 Schematic cross-sectional view of a modified example of the substance activation component. Figure 3 Schematic cross-sectional view of the substance activation component according to another embodiment of the present invention. Figure 4 It is from Figure 3 Schematic top view observed in the direction of arrow A. Figure 5 Explanation diagram for explaining the magnetic field lines of a cylindrical magnet. Figure 6 It is related to Figure 3 Schematic cross-sectional view of a modified example of the substance activation component. Figure 7 Image for explaining the experimental content using the substance activation component of the present invention. Figure 8 Diagram related to the experimental results using the substance activation component of the present invention. Figure 9 Diagram related to the experimental results for confirming the effect of the substance activation component of the present invention. Figure 10 Diagram related to the experimental results for confirming the effect of the substance activation component of the present invention. Figure 11 Diagram related to the experimental results for confirming the effect of the substance activation component of the present invention. Figure 12 Diagram related to the experimental results for confirming the effect of the substance activation component of the present invention. Detailed implementation mode

[0020] Hereinafter, the substance activation raw material according to an embodiment of the present invention will be described. In addition, the present invention is not limited by any of the following embodiments, and within the scope of the object of the present invention, modifications can be appropriately made and implemented. The substance activation raw material of the present invention is a raw material capable of generating electrons, and includes: powder of natural minerals containing radioactive substances; and powder of electron-generating substances, which generate electrons by using the alpha rays released from the natural minerals. In addition, it goes without saying that the powder of natural minerals and the powder of electron-generating substances are uniformly mixed to form the substance activation raw material of the present invention.

[0021] As the natural mineral containing radioactive substances, there is no particular limitation. For example, it can include radium ore, hokutolite, Badgastein ore, monazite, phosphate rock, columbite, tantalite, spectroite, pyrochlore, bastnäsite, cerium concentrate, zircon, curite, uranium titanomagnetite, uranium titanate, uraninite (pitchblende), anthropomorphic stone, autunite, carnotite, tyuyamunite, meta-tyuyamunite, tyuyamunite, liebigite, thorite, monazite-(Ce), thorium silicate, thorite, medonosite, allanite, tungsten ore, thorianite, hydrothorite, calcium silicate uranium ore, torbernite, uranophane, thoruranite, thorium uranate, thorite, and yellow barium lead uranium vanadate, etc.

[0022] In addition, as the electron generating substance that generates electrons by using the alpha rays released from natural minerals, for example, powders of titanium dioxide (TiO 2 ) can be used.

[0023] The smaller the average particle size of the powder of the natural mineral contained in the substance activation raw material of the present invention, the higher the effect can be obtained. For example, it is preferably set to 200 μm or less, more preferably set to 100 μm or less. Even more preferably, it is set to 10 μm or less. Similarly, the smaller the average particle size of the powder of the electron generating substance, the higher the effect can be obtained. For example, it is preferably set to 200 μm or less, more preferably set to 100 μm or less. Even more preferably, it is set to 10 μm or less.

[0024] In addition, regarding the substance activation raw material of the present invention, as long as it can generate an amount of alpha rays sufficient to activate the substance to be activated, the lower limit of the content of the natural ore is not particularly limited. The lower limit of the content of the natural ore is preferably 0.01 part by mass or more, more preferably 0.1 part by mass or more, and particularly preferably 1 part by mass or more with respect to 100 parts by mass of the substance activation raw material. In addition, as long as the generated radiation dose can be 0.2 μSv / h or less, the upper limit of the content of the natural ore is not particularly limited. The upper limit of the content of the natural ore is preferably 90 parts by mass or less, more preferably 85 parts by mass or less, and particularly preferably 80 parts by mass or less with respect to 100 parts by mass of the substance activation raw material.

[0025] In addition, regarding the substance activation raw material, it is preferable that the content of the electron generating substance that generates electrons using alpha rays released from natural minerals is a content that can maximize the ionization effect of alpha rays. In particular, the content of titanium dioxide contained in the electron generating substance of the present invention is preferably set to 1 part by mass or more and 15 parts by mass or less, for example, with respect to 100 parts by mass of the substance activation raw material. In addition, the substance activation raw material of the present invention may be configured to have at least one powder selected from lanthanum hexaboride (LaB6), black silicon dioxide, tungsten, metal silicon, molybdenum disulfide, metal germanium, gallium nitride (GaN), tourmaline, boron, and boron compounds, in addition to the powder of titanium dioxide, as the electron generating substance. Here, the content rate of lanthanum hexaboride is preferably set to 0.5 part by mass or more and 5 parts by mass or less, with respect to 100 parts by mass of the substance activation raw material. In addition, the content rate of black silicon dioxide is preferably set to 1 part by mass or more and 5 parts by mass or less, with respect to 100 parts by mass of the substance activation raw material. The content rate of tungsten is preferably set to 0.1 part by mass or more and 0.5 part by mass or less, the content rate of metal silicon is preferably set to 2 parts by mass or more and 5 parts by mass or less, with respect to 100 parts by mass of the substance activation raw material. The content rate of molybdenum disulfide is preferably set to 2 parts by mass or more and 5 parts by mass or less, the content rate of metal germanium is preferably set to 2 parts by mass or more and 5 parts by mass or less, with respect to 100 parts by mass of the substance activation raw material. The content rate of gallium nitride (GaN) is preferably set to 0.8 part by mass or more and 2 parts by mass or less, the content rate of tourmaline is preferably set to 2 parts by mass or more and 10 parts by mass or less, with respect to 100 parts by mass of the substance activation raw material. In addition, the content rate of boron is preferably set to 0.8 part by mass or more and 2 parts by mass or less, the content rate of boron compound is preferably set to 0.8 part by mass or more and 2 parts by mass or less, with respect to 100 parts by mass of the substance activation raw material. In addition, as the boron compound, for example, disodium octaborate tetrahydrate can be cited.

[0026] In addition, as the electron generating substance, it may be configured to contain a powder of metallic magnesium in addition to the powder of titanium dioxide. The average particle diameter of the powder of metallic magnesium is preferably set to 0.3 mm or more and 1.5 mm, more preferably set to 0.5 mm or more and 1.0 mm or less. In addition, the content of the powder of metallic magnesium is preferably set to 15 parts by mass or more and 35 parts by mass or less, particularly preferably set to 20 parts by mass or more and 30 parts by mass or less, with respect to 100 parts by mass of the substance activation raw material. In addition, as described above, by setting the average particle diameter of the powder of metallic magnesium to be much larger than the average particle diameter of the powder of the electron generating substance, a very large amount of powder of natural minerals comes into contact with the periphery of one powder of magnesium metal, and a larger amount of electrons can be released.

[0027] In addition, as the electron generating substance, it may be configured to contain, in addition to the titanium dioxide powder, a copper powder. The copper powder is preferably formed in a flake shape. In addition, the average particle size of the copper powder is preferably 10 μm or less, more preferably 1 μm or less. Since the copper powder has high conductivity, it can transfer electrons to the outside with high efficiency. In addition, the content of the copper powder is preferably set to 1 part by mass or more and 4 parts by mass or less with respect to 100 parts by mass of the substance activation raw material.

[0028] In addition, as the electron generating substance, it may be configured to contain, in addition to the titanium dioxide powder, a powder obtained by silver-plating the surface of the copper powder (silver-plated copper powder). The powder obtained by silver-plating the surface of the copper powder is preferably formed in a flake shape. In addition, the average particle size of the powder obtained by silver-plating the surface of the copper powder is preferably 10 μm or less, more preferably 1 μm or less. Since the powder obtained by silver-plating the surface of the copper powder also generates the release of electrons due to the bonding of dissimilar metals of silver and copper, the amount of released electrons is further increased. In addition, since the powder obtained by silver-plating the surface of the copper powder has excellent conductivity, it can transfer the electrons generated inside the electron generating material 52 to the outside with high efficiency. In addition, the content of the powder obtained by silver-plating the surface of the copper powder is preferably set to 5 parts by mass or more and 20 parts by mass or less, more preferably 8 parts by mass or more and 14 parts by mass or less with respect to 100 parts by mass of the substance activation raw material.

[0029] In addition, as the electron generating substance, it may be configured to contain, in addition to the titanium dioxide powder, a silver powder. The silver powder is preferably formed in a flake shape. In addition, the average particle size of the silver powder is preferably 10 μm or less, more preferably 1 μm or less. In addition, since the silver powder has excellent conductivity, it can transfer the electrons generated inside the electron generating material 52 to the outside with high efficiency. In addition, the content of the silver powder is preferably set to 8 parts by mass or more and 12 parts by mass or less with respect to 100 parts by mass of the substance activation raw material.

[0030] In addition, regarding the substance activation raw material of the present invention, it may be configured to further contain a powder of a conductive carbon substance such as graphite. The average particle size of the powder of the carbon substance is preferably 10 μm or less, more preferably 1 μm or less. In addition, the content of the powder of the carbon substance is preferably set to 1 part by mass or more and 5 parts by mass or less with respect to 100 parts by mass of the substance activation raw material. By further containing such a powder of a conductive carbon substance, the conductivity can be further improved, and electrons can be transferred to the outside with high efficiency.

[0031] In addition, regarding the material activation raw material of the present invention, it is preferably further mixed with a conductive fluidic binder. Such a fluidic binder is configured to include, for example, a powder of a metal raw material and a solvent. The fluidic binder can be dry and naturally dried, or can be non-dry and not naturally dried. In the case where the fluidic binder is configured to be dry, for example, a solvent that volatilizes by natural drying is used as the solvent. In addition, in the case where the fluidic binder is configured to be non-dry, for example, a non-dry oil such as non-dry grease or mineral oil can be used as the solvent. In addition, the average particle size of the powder of the metal raw material contained in the fluidic binder is preferably 200 μm or less.

[0032] By mixing the fluidic binder to form the material activation raw material, it is possible to maintain a state in which the powder of the natural ore and the powder of the electron-generating substance contained in the material activation raw material are uniformly dispersed. In addition, in the case where a dry fluidic binder is used, for example, after the fluidic material activation raw material is poured into a specified mold box, it is dried, so that the solvent contained in the fluidic binder volatilizes. As a result, the material activation raw material can be molded and cured into a desired shape. In addition, in the case where a non-dry fluidic binder is used, the material activation raw material can be configured to be in a fluidic state.

[0033] Here, as the conductive metal raw material contained in the fluidic binder, for example, at least one selected from zinc, molybdenum disulfide, and copper is preferably used. In addition, as a fluidic binder containing a powder of zinc, for example, a room-temperature electroplating coating containing zinc can be appropriately cited. Since the solvent contained in the room-temperature electroplating coating containing zinc volatilizes at room temperature and zinc is cured after volatilization, it is suitable for the case where the material activation raw material is molded and cured into a desired shape. In addition, since zinc is also a substance that generates electrons by the alpha rays released from natural minerals, in the material activation component obtained by molding and curing the material activation raw material, electrons are generated from the above-mentioned electron-generating substance and zinc by the alpha rays released from natural minerals, so the amount of electrons released increases. In addition, since zinc has conductivity, it is possible to efficiently transfer the electrons generated inside the material activation component to the outside of the material activation component.

[0034] In addition, as a fluidity binder for a powder containing molybdenum disulfide, for example, molybdenum disulfide grease can be appropriately cited. Since this molybdenum disulfide grease is a substance obtained by mixing molybdenum disulfide powder in a non-drying grease, it does not dry naturally, and the substance activation raw material maintains fluidity. A substance activation raw material containing such molybdenum disulfide grease as a fluidity binder can be used, for example, by attaching it to the tip of a screw component to be disassembled and assembled. In addition, molybdenum disulfide is also a substance that generates electrons using alpha rays released from natural minerals. In addition, copper grease obtained by mixing copper powder and non-drying grease can also be appropriately used.

[0035] In addition, regarding the substance activation raw material, the content of the fluidity binder is preferably 50 parts by mass or more and 75 parts by mass or less, for example, relative to 100 parts by mass of the substance activation raw material. In addition, in the case of using a dry fluidity binder, as long as it can maintain the shape after solvent evaporation and drying, for example, the shape in the dry state when drying a substance activation raw material having fluidity after coating, or the shape when drying a substance activation raw material having fluidity after flowing it into a specified mold box to form the substance activation raw material into a desired shape, the content is not particularly limited to the above numerical range. In addition, in the case of using a non-drying fluidity binder, if the substance activation raw material has fluidity, its content is not particularly limited to the above numerical range.

[0036] In addition, regarding the fluidity binder, the higher the content of the powder of the metal raw material, the better the concentration. In addition, in the case of using a dry fluidity binder, as long as it can maintain the shape after solvent evaporation and drying, for example, the shape in the dry state when drying a substance activation raw material having fluidity after coating, or the shape when drying a substance activation raw material having fluidity after flowing it into a specified mold box to form the substance activation raw material into a desired shape, in addition, in the case of using a non-drying fluidity binder, if the substance activation raw material has fluidity, its content is not particularly limited.

[0037] Next, the substance activation component 1 of the present invention will be described with reference to the accompanying drawings. In addition, the present invention is not limited by any of the following embodiments, and can be appropriately modified and implemented within the scope of the object of the present invention. In addition, each figure is enlarged and reduced locally for easy understanding of the configuration. The substance activation component 1 of the present invention is a component composed of the above-mentioned substance activation raw material. For example, as shown in the schematic cross-sectional view of the configuration, it includes an electron generation unit 2 and an electrode unit 3. Figure 1 As shown in the schematic cross-sectional view of the configuration, it includes an electron generation unit 2 and an electrode unit 3.

[0038] The electron generation unit 2 includes: a powder of natural minerals containing a radioactive substance; and a powder of an electron generation substance that generates electrons using alpha rays released from natural minerals.

[0039] As natural minerals containing radioactive substances, similar to the above, for example, radium ore, hokutolite, badgastein ore, monazite, phosphate ore, columbite, tantalite, spectrometerite, xanthochlore, cerium fluoride, cerium concentrate, zircon, uraninite, uraninite titanate, uraninite (pitchlite), anthropogonite, calcurranite, vanadate uraninite, calcurranite, calcurranite, calcurranite, uraninite, uraninite, titanite, thorium zirconite, xenotime, thorium silicate, thorium phosphate, medical stone, allantite, wolframite, thorite, hydrophosphate calcium thorite, calcium silicate uraninite, cuproclase, uraninite, thorium thorite, uraninite, thorium thorite, and yttrium vanadium barium lead ore.

[0040] In addition, as the electron generating material that generates electrons by utilizing alpha rays emitted from natural minerals, for example, titanium dioxide (TiO 2 ) and powder of at least one selected from lanthanum hexaboride (LaB6), black silica, metallic magnesium, copper, silver-plated copper, silver, tungsten, metallic silicon, molybdenum disulfide, metallic germanium, gallium nitride (GaN), tourmaline, boron, and boron compounds.

[0041] In addition, the average particle size of the powder of the natural mineral is preferably 200 μm or less, more preferably 100 μm or less, and further preferably 10 μm or less. The average particle size of the powder of the electron generating substance is preferably 200 μm or less, more preferably 100 μm or less, and further preferably 10 μm or less.

[0042] For example, a conductive fluid adhesive is further mixed with powder of a natural mineral containing a radioactive substance and powder of an electron generating substance that generates electrons by utilizing alpha rays released from the natural mineral, and stirred uniformly to thereby form a fluid material activation raw material, and then the fluid material activation raw material is applied to a sheet-like electrode portion 3 in a specified thickness to form the electron generating portion 2, and then another sheet-like electrode portion 3 is stacked and dried, thereby forming the electron generating portion 2.

[0043] As a fluid binder, for example, a room temperature electroplating paint containing zinc can be appropriately cited. The room temperature electroplating paint containing zinc can shape and solidify the material activation raw material into a desired shape because the solvent contained in the paint evaporates at room temperature and the zinc solidifies after volatilization.

[0044] Here, the electrode part 3 is a component electrically connected to the object to be substance-activated. As long as it can transfer the electrons generated by the electron generation part 2 to the object to be substance-activated, its raw material is not particularly limited. For example, raw materials with high electrical conductivity such as copper, silver, and gold are preferably used. From the perspective of cost, copper is more preferably used.

[0045] Here, the Figure 1 configuration of the substance activation component 1 shown in is configured as a sheet-like substance activation component 1 having a single-layer electron generation part 2, but it is not limited to such a configuration. As shown in the schematic cross-sectional view of the Figure 2 outline configuration, it can also be configured as a multi-layer type substance activation component 1 obtained by alternately laminating a sheet-like electron generation part 2 and a sheet-like electrode part 3. In addition, Figure 1 the configuration of the substance activation component 1 shown in is sheet-like, but there is no particular limitation on such a form. Of course, by flowing a substance activation raw material with fluidity into a specified mold box and then drying it, and drying the solvent of the fluidity binder, the substance activation component 1 can be formed in various forms (such as cylindrical, prismatic, bolt-shaped, box-shaped, curved-shaped, etc.).

[0046] In addition, as the substance activation component 1, as shown in the Figure 3 schematic cross-sectional view of the outline configuration and the Figure 3 top view observed from the arrow A direction of the Figure 4 shown, the following configuration can also be adopted: filling the above-mentioned substance activation raw material inside a cylindrical magnet 4 to form an electron generation part 2, and connecting the electrode part 3 to the magnet 4.

[0047] The magnet 4 is configured as a cylindrical magnet 4 with one end being the N pole and the other end being the S pole. In addition, as long as the electrode part 3 is configured to be connected to the magnet 4, there is no particular limitation. It is preferred that the electrode is connected to one end of the cylindrical magnet 4 on the N pole side. In particular, as shown in the Figure 3 , Figure 4 shown, it is particularly preferably configured as a plate-shaped electrode that connects to the entire area of the end face of one end of the magnet 4 on the N pole side and closes the opening on one end side of the cylindrical magnet 4. In addition, more preferably, the plate-shaped electrode is formed to have an area larger than the area surrounded by the outer peripheral contour line of one end of the cylindrical magnet 4.

[0048] Here, as the substance activation raw material filled inside the cylindrical magnet 4, it can only contain a powder of a natural mineral containing a radioactive substance and a powder of an electron generation substance that generates electrons using the alpha rays released from the natural mineral. In addition, it can also contain a fluidity binder with conductivity. In addition, as the fluidity binder, it can be dry or non-dry.

[0049] Thus, the substance activation component 1 formed by filling the substance activation raw material inside the cylindrical magnet 4 can transfer electrons to the substance to be activated at high speed because the electrons generated in the substance activation raw material move faster by using the magnetic field lines of the magnet 4, and the moving direction of the electrons is controlled by the magnetic field lines.

[0050] In addition, as Figure 5 shown, since the magnetic field lines of the magnet 4 come out from the N - pole side and enter the S - pole side, the electrode part 3 is configured to be connected to one end as the N - pole side, so that the electrons generated by the electron generation part 2 can be efficiently guided to the electrode and transferred to the substance to be activated. In particular, as Figure 3 , Figure 4 shown, from the viewpoint of efficiently transferring the electrons generated by the electron generation part 2 to the substance to be activated, a plate - shaped electrode connected to the entire area of the end face of one end of the magnet 4 as the N - pole side is preferably adopted. In addition, by forming the plate - shaped electrode to have an area larger than the area surrounded by the outer peripheral contour line of one end of the cylindrical magnet 4, the electrons moving along the magnetic field lines formed outside the magnet 4 can be transferred to the substance to be activated via the plate - shaped electrode. That is, the electrons released toward the outside of the magnet 4 can be efficiently transferred to the substance to be activated.

[0051] In addition, as Figure 6 shown in the schematic cross - sectional view of the configuration, it can also be configured to include an insulating component 5 that covers the side face part and the other end part side of the magnet 4. The raw material for forming the insulating component 5 is not particularly limited, and generally known insulating materials can be used. In addition, the insulating component 5 can be a detachable component like a rubber cover, or the surface of the magnet 4 can be covered and fixed with an insulating resin material so that it cannot be detached. By providing such an insulating component 5, the electrons generated in the electron generation part 2 can be effectively prevented from being released to the outside of the substance activation component 1, and the generated electrons can be effectively transferred toward the substance to be activated.

[0052] The substance activation component 1 with such a configuration is installed in a device in which a substance to be activated exists inside in various fields, so that the substance can be effectively activated. For example, the sheet - shaped substance activation component 1 is wound around the surface of the air duct of an automotive engine and fixed with a fixing member such as a bundling band. Thus, the electrons generated from the substance activation component 1 are transferred to the air molecules of the intake air flowing through the inside of the air duct, greatly promoting the activation of the air molecules. And if the activated intake air is supplied to the inside of the cylinder of the automotive engine, the fuel injected into the cylinder is sufficiently mixed with the activated intake air. Therefore, the combustion efficiency of the fuel in the cylinder is greatly improved, and the reduction of fuel consumption rate and the purification of exhaust gas can be promoted. In addition, since the substance activation component 1 is installed outside the air duct, it does not become a resistance when the engine intakes air.

[0053] In addition, by winding the substance activation component 1 around the outside of the exhaust pipe of an automobile, the electrons released from the substance activation component 1 are transferred to compounds such as carbon monoxide, carbon dioxide, and nitrogen oxides contained in the exhaust gas, and the activation of these compounds can be greatly promoted. These compounds are sent to the catalyst device in a state where they are greatly activated by the transferred electrons, so purification can be performed with very high efficiency. In addition, since the substance activation component 1 is wound around the outside of the exhaust pipe of the automobile, this component will not be damaged by the influence of high-temperature exhaust gas.

[0054] In addition, by winding the substance activation component 1 around the outside of the cylinder block of an automobile, the electrons released from the substance activation component 1 act on the intake air or exhaust gas of the automobile engine flowing through the inside of the cylinder block, and their activation can be greatly promoted. These intake air or exhaust gas are sent to the catalyst device in a state where they are greatly activated by the transferred electrons, so they are purified with very high efficiency.

[0055] In addition, the substance activation component 1 can also be used in a lubricating device for lubricating the sliding parts of a machine with lubricating oil. In order to reduce the friction between the sliding parts of the metals of the machine, lubricating oil is used, but such lubricating oil is affected by heat, worn metal powder, etc., and its lubricating ability and heat exchange ability gradually decrease. In addition, if metal wear powder accumulates in the oil filter, the passing ability of the lubricating oil decreases, and the lubricating performance further decreases. Therefore, by winding the substance activation component 1 in such a way as to be outside the container for storing the lubricating oil for lubricating the sliding parts of the machine or the pipe through which the lubricating oil flows, the electrons radiated from the substance activation component 1 act on the lubricating oil flowing through the inside of the lubricating device, and the activation of the lubricating oil is greatly promoted. The lubricating oil activated by the transferred electrons can flow smoothly between the metal wear powder and the like accumulated on the oil filter. Therefore, not only can the performance of the oil filter be maintained and the lubricating performance be improved, but also the burden on the oil pump can be reduced and the power loss can be decreased.

[0056] In addition, the material activation component 1 can also be used in a cooling device that uses a coolant to cool the heat-generating part of a machine. For example, in an engine, in order to effectively remove the heat generated by combustion from the cylinder block, the coolant is pressurized and circulated. However, if the coolant is pressurized and circulated, it will not only burden the pump, but also leak from the connection part of the pipe, or cause the hose to break. Therefore, by winding the material activation component 1 around the outside of a container that stores the coolant for cooling the heat-generating part of the machine or a pipe in which the coolant flows, the electrons emitted from the material activation component 1 act on the coolant flowing through the inside of the cooling device, greatly promoting the activation of the coolant. As a result, a coating film can be formed on the inner wall surface of the coolant circulation system, which can not only improve the heat transfer coefficient and improve the cooling efficiency, but also make the coolant laminar and flow smoothly, reducing the circulation resistance of the coolant. As a result, the circulation pressure of the coolant can be reduced, so that not only the burden on the pump and the power loss can be reduced, but also leakage from the connection part of the pipe, the breakage of the hose, etc. can be prevented. Furthermore, the coolant layer activated by the transfer of electrons also has the effect of preventing corrosion of the coolant circulation system and deterioration of rubber hoses and the like.

[0057] In addition, the material activation component 1 can also be used in a fuel supply device that supplies liquid or gaseous fuel to an internal combustion engine such as an engine. In general combustion, the vaporized liquid fuel or gaseous fuel is combined with oxygen in the combustion chamber to obtain heat energy. In order to efficiently obtain its energy from the liquid fuel or gaseous fuel, the fuel and the air must be fully mixed. Therefore, by winding the material activation component 1 around the outside of a container that stores the liquid fuel or gaseous fuel supplied to the internal combustion engine or a pipeline through which these fuels flow, the electrons generated from the material activation component 1 act on the above-mentioned fuel, greatly promoting the activation of the fuel. As a result, the particle size of the fuel when it is injected from the fuel injection valve and atomized can be made much finer than usual. As a result, the fuel and the air can be fully mixed in the combustion chamber, and the heat energy of the fuel can be fully obtained. This can be applied not only to gasoline but also to all petroleum products that help combustion.

[0058] In addition, the substance activation component 1 can also be used to form the moving blades of a turbine. By applying working fluids such as water in hydroelectric power generation, steam in thermal power generation, and oil in an automotive automatic transmission to the turbine blades respectively, rotational driving force can be obtained. However, when the fluid contacts the turbine blades, the resistance generated on the turbine blades increases as the velocity of the fluid increases. Therefore, if the velocity of the fluid is made too large, the energy transfer ability from the fluid to the turbine blades will be reduced. Thus, by winding the substance activation component 1 around the outside of the turbine blades or around the outside of the housing that houses the turbine blades inside, the electrons generated from the substance activation component 1 act on the above-mentioned fluid, greatly promoting the activation of the fluid. As a result, a laminar flow is formed on the surface of the moving blades of the turbine, and the fluid flows smoothly between the turbine blades. Therefore, the resistance generated on the turbine blades can be reduced, and rotational driving force can be obtained with high efficiency.

[0059] In addition, the substance activation component 1 can also be used in cooling devices such as air conditioners. The cooling devices of air conditioners and refrigerators vaporize the refrigerant in the evaporator, extract heat from the air in the living room or refrigerator, then compress the refrigerant in the condenser, and dissipate heat to the outside via the radiator. Therefore, in order to improve the cooling performance of refrigerators and air conditioners, it is necessary to improve the heat exchange efficiency of the refrigerant in the evaporator. Thus, by winding the substance activation component 1 around the evaporator, which is the passage for the refrigerant in the cooling device, or around the pipeline through which the refrigerant flows inside, the electrons generated from the substance activation component 1 act on the above-mentioned refrigerant, greatly promoting the activation of the refrigerant. As a result, the film of the activated refrigerant adheres closely to the metal inner wall surfaces of the evaporator and the pipeline. Therefore, the heat exchange efficiency between the metal inner wall surfaces of the evaporator and the pipeline and the refrigerant can be greatly improved.

[0060] In addition, the substance activation component 1 can also be used for a cleaning water storage container. Tap water is used as the solvent for detergents for cleaning tableware, etc. in ordinary households, etc. In order to improve the cleaning power, warm water has to be used, which has the drawback of incurring electricity costs and fuel costs. Thus, by winding the substance activation component 1 around the cleaning water storage container or around the pipeline through which the cleaning water flows, the electrons generated from the substance activation component 1 act on the fluid, greatly promoting the activation of the cleaning water. If the tap water that has been activated by receiving electrons is used as the solvent, then even at room temperature, the surfactant of the detergent effectively exhibits its active effect. As a result, the ability to clean tableware, laundry, etc. can be greatly improved. In addition, the tap water that has been activated by receiving electrons also has the effect of preventing corrosion inside the water pipes.

[0061] In addition, the substance activation component 1 can also be used for the growth of plants. For the growth of plants, in addition to sunlight and carbon dioxide in the atmosphere, water containing nutrients is also required. Moreover, in order to promote the growth of plants, it is preferable to increase the amount of water absorbed by the roots of the plants. As a method for this, there is a method of raising the temperature of the water, but in this method, it only reaches a certain level where the amount of water absorbed by the roots of the plants can be increased to a certain extent. Therefore, in order to increase the amount of water absorbed by the roots of the plants, by winding the substance activation component 1 around a supply water storage container containing water with nutrients supplied to the plants or on a pipeline through which the supply water flows inside, the electrons generated from the substance activation component 1 act on the above-mentioned fluid, greatly promoting the activation of the supply water and the like. Thereby, the water supplied to the plants and the nutrients contained in the water can be activated, and the thus-activated water and nutrients are easily absorbed by the root hairs of the plants, so the growth of the plants can be promoted. In addition, when bacteria and enzymes decompose humus soil, nitrogen compounds required by plants are generated. If highly activated water is supplied, the decomposition of humus soil is promoted, and the generation of nitrogen compounds is increased. Thereby, the growth of plants can be greatly promoted by such activated water that sufficiently dissolves nitrogen compounds.

[0062] In addition, the substance activation component 1 can also be used for the growth of animals. The growth of animals requires water which constitutes most of their bodies. The animals kept in zoos and the like obtain drinking water from tap water. However, during the period when the drinking water is stored in the supply water tank, the oxidation and deterioration of the drinking water are aggravated. Therefore, by winding the substance activation component 1 around the supply water tank or on the outer side of the pipeline through which the supply water flows inside, the electrons generated from the substance activation component 1 act on the supply water to activate it. The activated water is easily absorbed into the bodies of animals. In addition, since the oxidation-reduction potential is inhibited, it has an antioxidant effect, and in addition, it has an effect on improving the immune function and promoting growth.

[0063] In addition, the substance activation component 1 can also be used for the growth of fish and shellfish. Since the living environment of fish and shellfish is in water, the quality of the water is very important. When raising fish and shellfish, excreta are discharged into the same water tank as the living water, so if it is not purified regularly, the water quality will deteriorate. Therefore, by winding the substance activation component 1 around a supply water storage container for the water supplied to fish and shellfish, a circulating purification device, or on the outer side of the pipeline through which the supply water flows inside, the electrons generated from the substance activation component 1 act on the supply water to activate it. And the activated water is easily absorbed into the bodies of fish and shellfish. In addition, since the oxidation-reduction potential can be inhibited, it has an antioxidant effect, and in addition, it has an effect on improving the immune function and promoting growth.

[0064] In addition, the substance activation component 1 can also be used in a sewage treatment septic tank. In a septic tank that treats feces discharged from ordinary households, aerobic bacteria absorb oxygen in the air and oxidize and decompose organic substances. Therefore, by proliferating such aerobic bacteria, feces can be effectively treated. Thus, by winding the substance activation component 1 around the ventilation air supply pump or the outside of the pipeline through which ventilation air flows inside, the electrons generated from the substance activation component 1 act on the air passing through the pump or the air flowing through the pipeline, activating the air. As a result, activated air can be supplied to the septic tank, so that the aerobic bacteria that decompose feces can be activated, and sewage can be treated with higher efficiency.

[0065] In addition, the substance activation component 1 can also be used in a spraying device. When coating the body of an automobile, in order to form a high-quality coating surface with higher uniformity, it is necessary to reduce the particle size of the atomized paint. However, conventional spraying devices are structured to directly use air to atomize the paint, so it is difficult to further reduce the particle size of the atomized paint. Therefore, by winding the substance activation component 1 around the compressed air supply pump that sprays the paint and atomizes it or the outside of the pipeline through which compressed air flows inside, the electrons generated from the substance activation component 1 act on the air passing through the pump or the air flowing through the pipeline, activating the air, and using the activated compressed air to spray and atomize the paint, thereby promoting the mixing of air and paint and enabling the particle size of the atomized paint to become smaller. Therefore, a high-quality coating surface can be formed with higher uniformity.

[0066] In addition, it has been confirmed that by making the electrons released from the substance activation component 1 act on the fluid (gas, liquid, powder) moving in the pipe, the flow rate of the fluid becomes faster and the transfer efficiency is improved. For example, the time taken for transferring powder from a tanker truck to a tank in a factory through a pipeline can be shortened. This can be considered that by imparting electrons, static electricity is removed, and the frictional resistance between the powder and the pipeline is reduced, thereby making the flow rate faster. In addition, by winding the substance activation component 1 around the outside of the exhaust pipe of an automobile, etc., electrons are imparted to the exhaust gas, so that the exhaust speed of the exhaust gas also becomes faster, and the passage of the exhaust gas through the exhaust pipe is improved. As a result, the combustion efficiency of the engine is also improved.

[0067] The inventor conducted an experiment to confirm the effect of the substance activation component of the present invention, which will be described below. First, the substance activation component for the experiment was made into Figure 1The shape shown is formed into a rectangular parallelepiped shape with a thickness of 10 mm and a length × width = 40 mm × 60 mm. The powder of radium ore (natural ore), the powder of electron generating material and the room temperature plating solution containing zinc (a fluid binder with conductivity; a room temperature electroplating paint containing 96% zinc) are mixed and stirred thoroughly, poured into a mold, and taken out from the mold after drying. Electrode parts made of copper with a thickness of 0.02 mm (length × width = 40 mm × 60 mm) are stacked on both sides to form an electron generating part (material activation raw material). In addition, a wire is connected to the copper electrode parts arranged on both sides of the material activation part, and a plate-shaped terminal part is connected to the front end thereof, so that the electrons generated in the material activation part are transmitted from the terminal part to the activation object. In addition, the content of radium ore (natural ore) is 2 parts by mass relative to 100 parts by mass of the material activation raw material, the content of the electron generating material is 22.3 parts by mass relative to 100 parts by mass of the material activation raw material, and the content of the fluid binder is 75.7 parts by mass relative to 100 parts by mass of the material activation raw material. In addition, as the electron generating material, a powder mixture of titanium dioxide, metal magnesium, metal silicon, black silicon dioxide, lanthanum hexaboride, copper, and metal germanium is used. The content of titanium dioxide powder is 8 parts by mass relative to 100 parts by mass of the material activation raw material, the content of metal magnesium powder is 7.3 parts by mass relative to 100 parts by mass of the material activation raw material, the content of metal silicon is 3 parts by mass relative to 100 parts by mass of the material activation raw material, and the content of black silicon dioxide is 2 parts by mass relative to 100 parts by mass of the material activation raw material. In addition, the content of lanthanum hexaboride is 0.5 parts by mass relative to 100 parts by mass of the material activation raw material, and the content of copper powder is 2 parts by mass relative to 100 parts by mass of the material activation raw material. like Figure 7As shown, when the terminal part of the substance activation component formed in this way is connected to the high-pressure side pipe of the refrigerant gas of the air conditioner and electricity is applied, it is confirmed that the blowing temperature during refrigeration has decreased by 1 to 4 °C. Specifically, first, the temperature 20 minutes after the air conditioner was turned on was measured in the case of not using the substance activation component and in the case of using the substance activation component. The temperature measurement locations were the high-pressure side surface and the low-pressure side surface of the refrigerant gas pipe, and the indoor air outlet. In the case of not using the substance activation component, the temperatures of the high-pressure side and the low-pressure side of the refrigerant gas pipe were 17.5 °C and 22.7 °C respectively, and the temperature of the indoor air outlet was 14.8 °C. On the other hand, in the case of using the substance activation component, the temperatures of the high-pressure side and the low-pressure side of the refrigerant gas pipe were 15.5 °C and 22.0 °C respectively, and the temperature of the indoor air outlet was 11.6 °C. It was found that by using the substance activation component, the temperature of the indoor air outlet decreased by 3.2 °C. In addition, in this experiment, the indoor temperature was 29.5 °C, and the set temperature of the air conditioner was the energy-saving set temperature: 28 °C. It was also confirmed that: based on the lubricating effect, the noise level was also reduced. According to these phenomena, it is expected that electricity can be reduced by managing the set temperature. In addition, for all electrical products, by applying electricity to the equipment, the thermal conductivity is improved, the current becomes better, and thus the efficiency increases. Utilizing the friction resistance reduction effect helps to save electricity bills. The so-called flow of current is caused by the state of free electrons in the conductor, and it can be considered that the resistance value will slightly decrease by applying electricity. It was also confirmed that: in addition to air conditioners, even when electricity is applied to the refrigerant of refrigerators, mainly household refrigerators, their refrigeration capacity also increases. Next, an experiment was conducted in which the terminal part of the substance activation component for the experiment was connected to the motor of the fan and electricity was applied. Specifically, first, the change in the sound of the motor was measured in the case of not using the substance activation component and in the case of using the substance activation component. As a result, in the case of using the substance activation component, it was confirmed that the motor sound mainly decreased in the 54 Hz level, and it was confirmed that it decreased by 3.7 dB from -50.0 dB to -46.3 dB. Thus, in the case of using the substance activation component, it was confirmed that the burden on the motor, that is, the frictional resistance of the motor itself, decreased. In addition, it was confirmed that the wind noise of the fan blades also decreased. This can be considered that by removing static electricity with the substance activation component, it is possible to cut off the cycle in which static electricity is generated due to the rotation of the resin blades and friction with the air, and due to electrification, a greater frictional resistance is generated. As a result, the frictional resistance (mainly the frictional resistance generated by static electricity) associated with the rotation of the blades decreased.

[0068] In addition, it was confirmed that by imparting electrons released from the substance activation component 1 to water, the thermal conductivity of water increases. Specifically, ordinary tap water and tap water supplied with electrons from the substance activation component were prepared, and for each type of tap water, the change in water temperature with the passage of time (passage of heating time) under the same heating conditions was measured. The measurement results are shown in Table 1 below. Figure 8 The figure showing the measurement results. From these Table 1, Figure 8 and the figure, it can be seen that the tap water supplied with electrons from the substance activation component is heated more efficiently, and the thermal conductivity of water increases due to the supply of electrons. It was confirmed that: in particular, the thermal conductivity at 40 - 60 °C is increased by nearly 40% compared to water without electrons imparted. Thus, by increasing the thermal conductivity of water, the penetration power increases, the extraction power of the cooked food increases, and it can penetrate quickly. In addition, the penetration effect on plants was also confirmed. It was confirmed that if the harvested vegetables are immersed in water supplied with electrons, the water penetrates into the plants and the freshness is maintained. Also, when oil is put into water and stirred, and the separation state is confirmed in ordinary water and water supplied with electrons, the separation of the ordinary water side is faster, so the affinity between the water supplied with electrons and oil was also confirmed to increase.

[0069] [Table 1] In addition, it was confirmed that if electrons released from the substance activation component 1 are imparted to a cutting machine for metal processing, the cutting proceeds more smoothly and the cutting accuracy of the processed surface is improved. Usually, in a state without using lubricating oil, sintering occurs due to the contact between metals. Therefore, by using lubricating oil, the oil film of the lubricating oil is used to prevent metals from directly contacting each other to reduce friction. However, it was confirmed that instead of this lubricating oil, by imparting electrons, even if metals contact each other, it is difficult for sintering to occur due to the reduction of frictional resistance.

[0070] In addition, manufacturers recommend that automotive batteries be replaced usually after 3 years or 30,000 km of driving because the maximum capacity of the battery decreases. In the case of a battery whose maximum capacity has decreased to 80%, even if it is fully charged, it can only be charged to 80% of the electricity. However, by adding a few mL of an organic germanium solution supplied with electrons released from the substance activation component 1 to each cell of the battery, even if the battery capacity has decreased to 80%, as long as it undergoes normal operation for a few days, the maximum capacity of the battery can be restored to 100%. Also, regarding the same battery, the effect of extending the discharge time of the lithium-ion battery was also confirmed. This of course varies according to the current value, but in the case of rated use of this battery, it can be extended by 20 - 30%. It was also confirmed that: when charging the lithium-ion battery, if electrons are added from the negative terminal via the substance activation component 1, the capacity of the battery that has become old and decreased gradually increases.

[0071] In addition, the following two batteries were prepared as automotive batteries, and a battery recovery test was conducted. Battery 1: A battery that was replaced due to battery depletion and then left standing Battery 2: A battery that was in good condition and could be used In addition, Battery 1 had an open-circuit voltage of 8.8 V, 5 V when connected to a charger, which was lower than the reference voltage of 7.4 V and could not be restored by charging. Battery 2 had an open-circuit voltage of 12.2 V and had no problem with normal charging.

[0072] For these Batteries 1 and 2, battery fluid supplied with electrons was injected to the specified electrolyte level (5 cc per unit), and charging was carried out. Battery 1 was in a state where the charger circuit did not operate and charging was impossible. Battery 2 was fully charged after 7 hours of normal charging. Since Battery 1 had been left standing in a battery-depleted state for half a year, it was in a non-renewable state with sulfate crystallization on the electrodes and no current flowing at all. Therefore, Battery 2 was connected in parallel with Battery 1, and the voltage was raised above 10 V at which the charger operates to activate the charging circuit, and then Battery 2 was immediately removed. As a result, although the charging circuit operated, the battery electrodes of Battery 1 were damaged and no current flowed at all. Therefore, no change was observed in the non-chargeable state. However, during the process of repeating this state several times, current suddenly started to flow and charging became possible. After 5 hours, at the moment when charging was about 40% complete, foam blew out from the cap of the electrolyte and the internal electrolyte overflowed. Overall, nearly 20 cc overflowed. Before injecting the battery fluid supplied with electrons, since the liquid had entered above the upper level, the electrolyte was drained to adjust the level. At this time, the liquid was colorless and transparent. In contrast, the state of the overflowed liquid was a liquid that was blackened as a whole with black particles mixed in. After that, the charging of Battery 1 was completed in 4 hours.

[0073] The battery 1 was installed in a Daihatsu Move vehicle. When conducting an engine start test, it was confirmed that the engine started smoothly when the ignition key was turned. After that, the engine was temporarily turned off, the power windows were opened and closed, and then the engine was started again. This process was repeated 4 times, and it was confirmed that the engine started without problems. In addition, sulfates in the battery that usually cause over-discharge (a state where the battery is depleted, etc. and drops to 10V) cover the electrodes, and it is impossible to fully recover even with charging. Needless to say, for a battery that has dropped below 7.4V, it is not considered that the sulfates can be dissolved by charging due to sulfate crystallization in the first place. If the battery is left for half a year in a state where the electrodes are covered with the crystallized sulfates, it is absolutely impossible to regenerate. However, it was confirmed that by using the substance activation component of the present invention, even such a battery can be recovered without problems. In addition, one week after the above test, a battery installation test was conducted. With the air conditioner always on, there were no problems even during about half-day operation each of day and night. The engine starting condition was also very good, and the state was such that the dimming effect of the headlamps could not be felt at all during idling.

[0074] In addition, using a DELICA D5 manufactured by Mitsubishi Motors Corporation, the change in the engine sound during climbing was measured in the case of installing the substance activation component on the engine and the case of not installing the substance activation component on the engine. In Figure 9 and Figure 10 the measurement results are shown. In addition, in Figure 9 the measurement results in the case of not installing the substance activation component on the engine are shown, and in Figure 10 the measurement results in the case of installing the substance activation component on the engine are shown. The noise level in the case of not installing the substance activation component on the engine was 60.7 dB. In contrast, the noise level in the case of installing the substance activation component on the engine was 48.7 dB, and it can be seen that the noise level decreased by 12 dB. In addition, in Figure 11 and Figure 12 the measurement results related to the frequency distribution are shown. In addition, in Figure 11 the measurement results in the case of not installing the substance activation component on the engine are shown, Figure 12 and in Figure 11 、 Figure 12 it can be confirmed that the engine sound at low frequencies below 150 Hz decreased.

[0075] In addition, it was confirmed that by applying electricity during the incubation of chicken eggs, a state was achieved where the utilization rate of the egg yolk during hatching was approximately close to 100%. If a blood test was conducted on the chicks, the mRNA value of the spleen immune index increased, and the body weight also increased compared to the standard value. It is considered that the impact on the hemagglutination antibody titer of the chicks' foreign ridge blood cells and the expression of spleen immune-related genes is relatively large. Even in the case of humans, it was confirmed by a blood flow microscope that if electricity was applied to the ankle, the blood flow at the tips of the toes increased within just 10 seconds, and it was confirmed that the surface temperature of the back of the hand rose by 2 - 4°C on average within several tens of minutes.

[0076] Furthermore, the inventor conducted an experiment to confirm the effect of the non-drying substance activation raw material for non-natural drying, which will be described below. First, 4 types of non-drying substance activation raw materials for the experiment (Sample 1 - Sample 4) were prepared. Table 2 shows the content rates of the respective raw materials contained in each non-drying substance activation raw material.

[0077] [Table 2] Here, the molybdenum disulfide slurry is a fluid binder, and a slurry containing molybdenum disulfide powder with an average particle size of 1 μm in mineral oil as the base oil was used. Additionally, for Sample 1 and Sample 2, the content of molybdenum disulfide powder in the molybdenum disulfide slurry was 30 parts by mass relative to 100 parts by mass of the molybdenum disulfide slurry, and for Sample 3 and Sample 4, the content of molybdenum disulfide powder in the molybdenum disulfide slurry was 50 parts by mass relative to 100 parts by mass of the molybdenum disulfide slurry. Also, the average particle size of the titanium dioxide powder, metallic silicon powder, black silicon dioxide powder, copper powder, lanthanum hexaboride (LaB6) powder, gallium nitride (GaN) powder, and tourmaline powder is 1 μm or less.

[0078] The non-drying substance activation raw materials of the above-mentioned various samples were coated on the capacitors and transistors of an audio device (manufactured by DENON: CD player: DCD - 1650AR), and multiple people (10 people) listened to the music played by the audio, and a sensory test was conducted on whether they felt a change in the sound. Additionally, a sensory test was also conducted simultaneously in the state where the non-drying substance activation raw material was not coated. As a result, compared with the case where the non-drying substance activation raw material was not coated, the following evaluations were obtained for the case where the non-drying substance activation raw materials of various samples were coated: the transparency of the sound increased, and in addition, there was a full sense of presence and it sounded vivid. This is considered to be the effect obtained because the electrons released from the non-drying substance activation raw material and transmitted to the audio device reduced the mechanical noise emitted from the audio device and the noise coming around from the power supply.

[0079] In addition, compared with the case where Sample 1 was coated, in the case where Sample 2 was coated, an effect of further increasing the transparency of the sound, etc. was obtained. It is considered that this is the effect obtained by increasing the content of titanium dioxide and including gallium nitride. In addition, compared with the case where Sample 2 was coated, in the case where Sample 3 was coated, a result of better sound quality, increased transparency of the sound, and increased sense of presence was obtained. It is considered that this largely reflects the effect brought about by the increase in the content of molybdenum disulfide powder in the molybdenum disulfide paste and the further improvement of conductivity. In addition, it is considered to be the effect obtained by including lanthanum hexaboride powder. Furthermore, compared with the case where Sample 3 was coated, in the case where Sample 4 was coated, the following results were obtained: the sound quality became significantly better, the transparency of the sound and the sense of presence increased, and the quietness of the quiet part where no sound is played in the music was also good. It is considered that this is the effect of increasing the content of titanium dioxide.

[0080] In addition, the inventor coated the non-drying substance activation raw materials of Samples 1 to 4 described above on the power supply related device of a milling machine that rotates a cutting tool to cut metals, etc., and confirmed whether the machining accuracy changed and whether the mechanical operation sound changed. As a result, compared with the case where no non-drying substance activation raw material was coated, in the case where the non-drying substance activation raw material of each sample was coated, it was confirmed that the machining accuracy was improved, and in addition, the mechanical operation sound became quieter. It is considered that this is the effect obtained by the action of electrons released from the non-drying substance activation raw material and transmitted to the milling machine, the reduction of the frictional resistance between the cutting tool and the workpiece, and as a result, the reduction of the vibration of the rotating cutting tool. In addition, it was confirmed that: compared with Sample 1, the above effect of Sample 2 was greater, and in addition, compared with Sample 2, the above effect of Sample 3 was greater. Furthermore, it was confirmed that: compared with Sample 3, Sample 4 showed a greater above effect.

[0081] In addition, the inventor conducted a confirmation test on the change in the startup time of a tower personal computer (OS: Windows 10) self-made 15 years ago, by coating the non-drying substance activation raw material of Sample 1 on the fixed capacitor of the motherboard (MotherBoard). As a result of this confirmation test, it was confirmed that the startup time was 25 seconds before coating, and in contrast, it changed to 15 seconds after coating. In addition, the coating position of the non-drying substance activation raw material for the fixed capacitor was the electrode part of the capacitor on the back side of the printed circuit board. Furthermore, as a result of coating the non-drying substance activation raw material of Sample 1 on the solid capacitors near the CPU fan and the memory of this personal computer, an improvement in quietness and body sensation speed was confirmed. From this result, it can be seen that according to the electronic generation paste of the present invention, the operation speed and quietness of the computer can be improved. Description of reference numerals:

[0082] 1: Substance activation component; 2: Electron generation part; 3: Electrode part; 4: Magnet; 5: Insulating component.

Claims

1. A material activation raw material, characterized in that: The material activation raw material includes: powder of natural mineral containing radioactive material; and powder of electron generating material which generates electrons by using alpha rays released from the natural mineral.

2. The material activation raw material according to claim 1, characterized in that: The powder of the electron generating material comprises: powder of titanium dioxide; and powder of at least one selected from lanthanum hexaboride, black silicon dioxide, metal magnesium, tungsten, metal silicon, molybdenum disulfide and metal germanium.

3. The material activation raw material according to claim 1 or 2, characterized in that: The average particle size of the natural mineral powder is less than 200 μm. The average particle size of the powder of the electron generating substance is 200 μm or less.

4. The material activation raw material according to claim 1 or 2, characterized in that: The material activating raw material further comprises a fluid binder having electrical conductivity.

5. The material activation raw material according to claim 4, characterized in that: The flowable adhesive is non-drying.

6. The material activation raw material according to claim 4, characterized in that: The flowable adhesive is dry.

7. The material activation raw material according to claim 4, characterized in that: The fluid binder comprises powder of at least one selected from the group consisting of zinc, molybdenum disulfide and copper.

8. A substance activation component, characterized in that: The substance activation component comprises: The electron generating unit includes: a powder of a natural mineral containing a radioactive substance; and a powder of an electron generating substance that generates electrons using alpha rays emitted from the natural mineral; as well as The electrode part is connected to the electron generating part.

9. The substance activation component according to claim 8, characterized in that: The powder of the electron generating material comprises: powder of titanium dioxide; and powder of at least one selected from lanthanum hexaboride, black silicon dioxide, metal magnesium, tungsten, metal silicon, molybdenum disulfide and metal germanium.

10. The substance activation component according to claim 8 or 9, characterized in that: The average particle size of the natural mineral powder is less than 200 μm. The average particle size of the powder of the electron generating substance is 200 μm or less.

11. A substance activation component, characterized in that: The substance activation component comprises: A material activation raw material, comprising: a powder of a natural mineral containing a radioactive substance; and a powder of an electron generating substance, which generates electrons by utilizing alpha rays emitted from the natural mineral; and A cylindrical magnet with an N pole at one end and an S pole at the other end. The material activating member is configured by filling the material activating raw material inside the cylindrical magnet.

12. The substance activation component according to claim 11, characterized in that: The powder of the electron generating material comprises: powder of titanium dioxide; and powder of at least one selected from lanthanum hexaboride, black silicon dioxide, metal magnesium, tungsten, metal silicon, molybdenum disulfide and metal germanium.

13. The substance activation component according to claim 11 or 12, characterized in that: An electrode portion is connected to the one end of the cylindrical magnet that is the N-pole side.

14. The substance activation component according to claim 13, characterized in that: The electrode portion is a plate-shaped electrode connected to the entire end surface of the one end of the magnet.

15. The substance activation component according to claim 14, characterized in that: The plate-shaped electrode is formed to have an area larger than an area surrounded by an outer peripheral contour line of one end of the magnet.

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