Method for producing material-activating raw material and method for producing material-activating member

Abstract

Provided are a simple method for producing a material activation raw material capable of exhibiting a greater material activation effect, and a method for producing a material activation member. The method for producing a material-activating raw material includes mixing and stirring a powder of a natural mineral containing a radioactive substance, a powder of an electron-generating substance that generates electrons by alpha rays released from the natural mineral, and a dry flowable binder to form a material-activating raw material having flowability.

Description

Technical Field

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

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

[0003] The radiation generated by such a substance activation component ionizes substances such as combustion air and combustion exhaust gas that are the objects to be activated. 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 substance activation components exhibit certain excellent effects, it is desired to develop a method for manufacturing a new substance activation raw material and a substance activation component that can exhibit a further substance activation effect by a simple method.

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

[0007] The above object of the present invention is achieved by a method for manufacturing a substance activation raw material, the method for manufacturing the substance activation raw material mixing and stirring a powder of a natural mineral containing a radioactive substance, a powder of an electron generating substance that generates electrons by using alpha rays released from the natural mineral, and a dry flowable binder to form a flowable substance activation raw material.

[0008] In addition, the above object of the present invention is achieved by a method for manufacturing a substance activation raw material, the method for manufacturing the substance activation raw material mixing and stirring a powder of a natural mineral containing a radioactive substance, a powder of an electron generating substance that generates electrons by using alpha rays released from the natural mineral, and a non-drying flowable binder to form a flowable substance activation raw material.

[0009] Regarding the manufacturing method of the substance activation raw material, preferably, the powder of the electron generating substance includes: the powder of titanium dioxide; and the powder of at least one selected from lanthanum hexaboride, black silica, metallic magnesium, tungsten, metallic silicon, molybdenum disulfide, and germanium metal.

[0010] 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 generating substance is 200 μm or less.

[0011] In addition, preferably, the dry flowable binder has conductivity.

[0012] In addition, preferably, the dry flowable binder includes the powder of at least one selected from zinc, molybdenum disulfide, and copper.

[0013] In addition, preferably, the dry flowable binder is a normal temperature plating solution containing zinc.

[0014] In addition, preferably, the non-drying flowable binder has conductivity.

[0015] In addition, preferably, the non-drying flowable binder includes the powder of at least one selected from zinc, molybdenum disulfide, and copper.

[0016] In addition, preferably, the non-drying flowable binder is molybdenum disulfide grease.

[0017] In addition, the object of the present invention is achieved by the manufacturing method of the substance activation component. The manufacturing method of the substance activation component includes: a substance activation raw material forming step of mixing and stirring the powder of the natural mineral containing a radioactive substance, the powder of the electron generating substance that generates electrons by using the alpha rays released from the natural mineral, and the dry flowable binder to form a flowable substance activation raw material; a casting into a mold step of casting the flowable substance activation raw material into a mold; and a drying step of drying the substance activation raw material cast into the mold.

[0018] In addition, the object of the present invention is achieved by the manufacturing method of the substance activation component. The manufacturing method of the substance activation component includes: a substance activation raw material forming step of mixing and stirring the powder of the natural mineral containing a radioactive substance, the powder of the electron generating substance that generates electrons by using the alpha rays released from the natural mineral, and the dry flowable binder to form a flowable substance activation raw material; and a substance activation component filling step of filling the flowable substance activation raw material into the inside of a cylindrical magnet with one end being the N pole and the other end being the S pole.

[0019] In addition, the object of the present invention is achieved by a method for manufacturing a substance activation component, and the method for manufacturing the substance activation component includes: a substance activation raw material forming step of mixing and stirring a powder of a natural mineral containing a radioactive substance, a powder of an electron generating substance that generates electrons by using alpha rays released from the natural mineral, a powder of a ferrite magnet raw material, and a dry flowable binder to form a flowable substance activation raw material; a charging into a mold step of charging the flowable substance activation raw material into a mold; a drying step of drying the substance activation raw material charged into the mold; and a magnetization step of magnetizing the dried substance activation raw material.

[0020] Regarding the above method for manufacturing a substance activation component, 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 silicon dioxide, metallic magnesium, tungsten, metallic silicon, molybdenum disulfide, and germanium metal.

[0021] 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 generating substance is 200 μm or less.

[0022] In addition, preferably, the flowable binder has conductivity.

[0023] In addition, preferably, the flowable binder includes a powder of at least one selected from zinc, molybdenum disulfide, and copper.

[0024] In addition, preferably, the flowable binder is a room temperature plating solution containing zinc.

[0025] In addition, the object of the present invention is achieved by a method for manufacturing a substance activation component, and the method for manufacturing the substance activation component includes: a substance activation raw material forming step of mixing 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 to form a substance activation raw material; a charging into a mold step of charging the substance activation raw material into a mold; and a compression molding step of compression molding the substance activation raw material charged into the mold. Advantages of the Invention

[0026] According to the present invention, it is possible to provide a method for manufacturing a substance activation raw material and a substance activation component that can exert a greater substance activation effect by a simple method. Brief Description of the Drawings

[0027] Figure 1 It is a block diagram for explaining the method for manufacturing the first substance activation component of the present invention. Figure 2It is a block diagram for explaining a manufacturing method of a second substance activation component of the present invention. Figure 3 It is a schematic cross-sectional view for explaining a substance activation component manufactured by a manufacturing method of a third substance activation component of the present invention. Figure 4 It is from Figure 3 A schematic top view observed in the direction of arrow A. Figure 5 It is an explanatory diagram for explaining the magnetic field lines of a cylindrical magnet. Figure 6 It is a schematic cross-sectional view for explaining a modification related to the manufacturing method of a third substance activation component of the present invention. Figure 7 It is a block diagram for explaining a manufacturing method of a third substance activation component of the present invention. Figure 8 It is a block diagram for explaining a manufacturing method of a fourth substance activation component of the present invention. Figure 9 It is a schematic cross-sectional view for explaining a substance activation component for experiments. Figure 10 It is an image for explaining the experimental content using a substance activation component manufactured by the manufacturing method of the present invention. Figure 11 It is a graph related to the experimental results using a substance activation component manufactured by the manufacturing method of the present invention. Figure 12 It is a graph related to the experimental results for confirming the effect of a substance activation component manufactured by the manufacturing method of the present invention. Figure 13 It is a graph related to the experimental results for confirming the effect of a substance activation component manufactured by the manufacturing method of the present invention. Figure 14 It is a graph related to the experimental results for confirming the effect of a substance activation component manufactured by the manufacturing method of the present invention. Figure 15 It is a graph related to the experimental results for confirming the effect of a substance activation component manufactured by the manufacturing method of the present invention. Detailed implementation mode

[0028] Hereinafter, a method for manufacturing a substance activation raw material according to a first embodiment of the present invention will be described. 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. The method for manufacturing a substance activation raw material according to the first embodiment of the present invention is as follows: A powder of a natural mineral containing a radioactive substance, a powder of an electron generating substance that generates electrons by alpha rays released from the natural mineral, and a dry fluid binder are mixed and stirred to form a fluid substance activation raw material. In addition, it goes without saying that the powder of the natural mineral, the powder of the electron generating substance, and the dry fluid binder are uniformly mixed to constitute the substance activation raw material.

[0029] The natural mineral containing a radioactive substance is not particularly limited. For example, it can be cited as radium ore, hokutolite, badgastein ore, monazite, phosphate rock, columbite, tantalite, spectroite, pyrochlore, bastnäsite, cerium concentrate, zircon, curite, uranium titanomagnetite, uranium titanate, uraninite (pitchblende), humanite, autunite, carnotite, tyuyamunite, meta-tyuyamunite, tyuyamunite, metatorbernite, thorite, xenotime, thorium silicate, monazite-(Ce), shungite, allanite, tungsten ore, thorianite, hydrothorite, calcium uranium silicate, cuproautunite, uranophane, thoruranite, uranium thorite, thorite, and yellow barium lead uranium vanadate, etc.

[0030] In addition, as the electron generating substance that generates electrons by alpha rays released from the natural mineral, for example, a powder of titanium dioxide (TiO 2 ) can be used.

[0031] In addition, 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 parts by mass or more, more preferably 0.1 parts 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.

[0032] In addition, it is preferable that the content of the electron-generating substance that generates electrons by using the alpha rays released from natural minerals be a content that can maximize the ionization effect of the 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, relative 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, as the electron-generating substance, a powder containing at least one selected from lanthanum hexaboride (LaB6), black silicon dioxide, tungsten, metallic silicon, molybdenum disulfide, metallic germanium, gallium nitride (GaN), tourmaline, boron, and boron compounds, in addition to the powder of titanium dioxide. 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 relative 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 relative 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 relative to 100 parts by mass of the substance activation raw material, and the content rate of metallic silicon is preferably set to 2 parts by mass or more and 5 parts by mass or less relative 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 relative to 100 parts by mass of the substance activation raw material, and the content rate of metallic germanium is preferably set to 2 parts by mass or more and 5 parts by mass or less relative 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 relative to 100 parts by mass of the substance activation raw material, and the content rate of tourmaline is preferably set to 2 parts by mass or more and 10 parts by mass or less relative 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 relative to 100 parts by mass of the substance activation raw material, and the content rate of the boron compound is preferably set to 0.8 part by mass or more and 2 parts by mass or less relative 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.

[0033] In addition, the smaller the average particle size of the powder of the natural mineral used, 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.

[0034] In addition, as the electron generating substance, it may be configured to contain, in addition to the titanium dioxide powder, a magnesium metal powder. The average particle size of the magnesium metal powder is preferably set to be 0.3 mm or more and 1.5 mm, more preferably set to be 0.5 mm or more and 1.0 mm or less. In addition, the content of the magnesium metal powder is preferably set to be 15 parts by mass or more and 35 parts by mass or less, particularly preferably set to be 20 parts by mass or more and 30 parts by mass or less, based on 100 parts by mass of the substance activation raw material. In addition, as described above, by setting the average particle size of the magnesium metal powder to be much larger than that of the electron generating substance powder, a very large number of natural mineral powders come into contact with the periphery of one magnesium metal powder, and a larger amount of electrons can be released.

[0035] 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 efficiently transfer electrons to the outside. In addition, the content of the copper powder is preferably set to be 1 part by mass or more and 4 parts by mass or less based on 100 parts by mass of the substance activation raw material.

[0036] 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 efficiently transfer the electrons generated inside the electron generating material 52 to the outside. In addition, the content of the powder obtained by silver-plating the surface of the copper powder is preferably set to be 5 parts by mass or more and 20 parts by mass or less, more preferably set to be 8 parts by mass or more and 14 parts by mass or less, based on 100 parts by mass of the substance activation raw material.

[0037] 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 efficiently transfer the electrons generated inside the electron generating material 52 to the outside. In addition, the content of the silver powder is preferably set to be 8 parts by mass or more and 12 parts by mass or less based on 100 parts by mass of the substance activation raw material.

[0038] In addition, the material activation raw material of the present invention may also be configured to further include a powder of a conductive carbon material such as graphite. The average particle size of the powder of the carbon material is preferably 10 μm or less, more preferably 1 μm or less. In addition, the content of the powder of the carbon material is preferably set to 1 part by mass or more and 5 parts by mass or less relative to 100 parts by mass of the material activation raw material. By further including such a powder of a conductive carbon material, the conductivity can be further improved, and electrons can be efficiently transferred to the outside.

[0039] In addition, the fluidity binder is a dry binder that dries naturally and various substances can be used. For example, various binders such as an acrylic resin binder, a polycarbonate resin binder, and a polyester resin binder can be used. By mixing the fluidity binder to form the material activation raw material, the 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 can be maintained. In addition, in the case of using a dry fluidity binder, for example, after flowing the fluid material activation raw material into a predetermined mold box, it is dried, so that the solvent contained in the fluidity binder volatilizes, and as a result, the material activation raw material can be molded and solidified into a desired shape. In addition, without using a mold box, for example, the material activation raw material is coated on the upper surface of the electrode plate or the object to be activated with a predetermined thickness, and the material activation raw material is dried, so that a material activation component that releases electrons can be formed.

[0040] In addition, as the dry fluidity binder, it is more preferable to use a fluidity binder having conductivity. Such a fluidity binder can be used, for example, a binder obtained by using a binder that volatilizes by natural drying as a solvent and mixing a powder of a metal raw material in the solvent. In addition, the average particle size of the powder of the metal raw material contained in the fluidity binder is preferably 200 μm or less.

[0041] In addition, 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 material activation raw material. In addition, in the case of using a dry fluidity binder, as long as it can maintain the shape after the solvent volatilizes and dries, for example, the shape in the dry state when the fluid material activation raw material is coated and dried, or the shape when the fluid material activation raw material is flowed into a predetermined mold box and dried to mold the material activation raw material into a desired shape, it is not particularly limited to the above numerical range.

[0042] 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, it is only necessary that the shape can be maintained after the solvent has volatilized and dried, for example, the shape in the dry state when drying after coating the active material of the fluid substance, or the shape when the active material of the fluid substance is caused to flow into a specified mold box and then dried to form the active material into a desired shape.

[0043] Here, as the conductive metal raw material contained in the fluidity binder, for example, at least one selected from zinc, molybdenum disulfide, and copper is preferably used. As the fluidity binder containing zinc powder, for example, a room-temperature electroplating coating containing zinc can be appropriately cited. Since the solvent contained in this room-temperature electroplating coating containing zinc volatilizes at room temperature and zinc solidifies after volatilization, it is suitable for the case where the active material of the substance is formed into a desired shape and firmly solidified. In addition, since zinc is also a substance that generates electrons by the alpha rays released from natural minerals, the active material component obtained by forming and solidifying the active material of the substance becomes a substance that generates electrons from titanium dioxide and zinc by the alpha rays released from natural minerals, so the amount of electrons released increases. In addition, since zinc has conductivity, it can efficiently transfer the electrons generated inside the active material component to the outside of the active material component.

[0044] Next, the manufacturing method of the active material of the second embodiment of the present invention will be described. 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. The manufacturing method of the active material of the second embodiment of the present invention mixes and stirs the powder of the natural mineral containing the radioactive substance, the powder of the electron-generating substance that generates electrons by the alpha rays released from the natural mineral, and the non-drying fluidity binder to form a fluid active material. In addition, it goes without saying that the powder of the natural mineral, the powder of the electron-generating substance, and the non-drying fluidity binder are uniformly mixed to constitute the active material.

[0045] Here, for the natural ore and the electron-generating substance contained in the active material of the second embodiment, the same natural ore and electron-generating substance as those described in the manufacturing method of the active material of the first embodiment above can be used, so the detailed description is omitted.

[0046] In the method for manufacturing a substance activation raw material according to the second embodiment, the fluid binder used has the property of non-drying and does not dry unnaturally. As such a fluid binder, various non-drying oils such as non-drying grease can be used. By mixing the fluid binder to form the substance 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 substance activation raw material are uniformly dispersed. When a non-drying fluid binder is used, the substance activation raw material can be configured to be in a state of not drying unnaturally and always having fluidity. For example, the substance activation raw material can be attached to the tip of a disassembled screw part for use.

[0047] In addition, in the method for manufacturing a substance activation raw material according to the second embodiment, as the non-drying fluid binder, it is more preferable to use a fluid binder having conductivity. Such a fluid binder can be, for example, a binder obtained by using a non-drying oil such as non-drying grease as a solvent and mixing a powder of a metal raw material in the solvent. In addition, the average particle diameter of the powder of the metal raw material contained in the fluid binder is preferably 200 μm or less.

[0048] Here, as the metal raw material contained in the above fluid binder, similar to that described in the method for manufacturing a substance activation raw material according to the first embodiment, for example, at least one selected from zinc, molybdenum disulfide, and copper is preferable. In addition, as a fluid binder containing a powder of molybdenum disulfide, for example, molybdenum disulfide grease can be appropriately cited. Since this molybdenum disulfide grease is obtained by mixing molybdenum disulfide powder in the non-drying grease, it does not dry unnaturally and the substance activation raw material maintains fluidity. In addition, copper grease obtained by mixing copper powder in non-drying grease can also be appropriately used.

[0049] In addition, the content of the fluid binder is, for example, preferably 50 parts by mass or more and 75 parts by mass or less with respect to 100 parts by mass of the substance activation raw material. In addition, when a dry fluid binder is used, as long as it can maintain the shape after the solvent has volatilized and dried, for example, the shape in the dry state when the fluid substance activation raw material is coated and then dried, or the shape when the fluid substance activation raw material is poured into a specified mold box and then dried to form the substance activation raw material into a desired shape, the content is not particularly limited to the above numerical range.

[0050] In addition, regarding the fluid binder, the higher the content of the powder of the metal raw material, the better the concentration. In addition, when a non-drying fluid binder is used, if the substance activation raw material has fluidity, its content is not particularly limited.

[0051] According to such a method for manufacturing a substance activation raw material, it is possible to very simply manufacture a substance activation raw material that can exhibit a greater activation effect of the substance.

[0052] Next, a first manufacturing method of the substance activation component 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, it can be implemented with appropriate modifications. As Figure 1 shown in the block diagram, the first manufacturing method of the substance activation component includes a substance activation raw material forming step S11, a charging into a mold box step S12, and a drying step S13.

[0053] The substance activation raw material forming step S11 is a process of forming the above-mentioned substance activation raw material, which is a process of mixing and stirring a powder of a natural mineral containing a radioactive substance, a powder of an electron generating substance that generates electrons using alpha rays released from the natural mineral, and a dry fluid binder to form a fluid substance activation raw material.

[0054] Here, as the fluid binder used in the substance activation raw material forming step S11, it is more preferable to use a fluid binder having conductivity. As the dry fluid binder having conductivity, it is particularly preferable to use a room temperature plating solution containing zinc.

[0055] The charging into a mold box step S12 is a process of charging the fluid substance activation raw material into a mold box having a specified shape. There is no particular limitation on the shape of the mold box, and various mold boxes can be used.

[0056] The drying step S13 is a process of drying the substance activation raw material charged into the mold box. In this drying step S13, the substance activation raw material can be dried by natural drying, or the substance activation raw material can be dried by heating.

[0057] After the drying step S13 is completed, the dried and formed substance activation raw material is taken out from the mold box, thereby completing the substance activation component. In addition, by connecting the electrode part to the substance activation component, the electrons generated by the substance activation component can be efficiently transmitted to the substance to be activated. There is no particular limitation on the raw material for forming the electrode part. For example, it is preferable to use a raw material having high conductivity such as copper, silver, or gold. From the aspect of cost, it is more preferable to use copper. In addition, there is no particular limitation on the connection method between the substance activation component and the electrode part. For example, they can be connected by a conductive adhesive, or the substance activation component can be simply placed on the plate-shaped electrode part and brought into contact with each other for connection.

[0058] In addition, as required, as a subsequent process to the drying step S13, it may include a compression molding step of compression molding the substance activation raw material put into the mold box. In addition, when configured to include the compression molding step, it is preferably not to completely dry the substance activation raw material in the mold box in the above drying step S13, but to semi-dry the substance activation raw material to such an extent that it can be deformed during compression.

[0059] According to such a first manufacturing method of the substance activation component, it is possible to very simply manufacture a substance activation component that can exert a greater activation effect of the substance in various forms.

[0060] Next, a second manufacturing method of the substance activation component as the manufacturing method 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, it can be appropriately modified and implemented. This second manufacturing method of the substance activation component is a manufacturing method of a substance activation component that can effectively transfer the generated electrons to the substance activation object by using magnetic field lines, as Figure 2 shown in the block diagram, includes a substance activation raw material forming step S21 and a substance activation component filling step S22.

[0061] The substance activation raw material forming step S21 is a process of forming the above substance activation raw material, and is a process of mixing and stirring a powder of a natural mineral containing a radioactive substance, a powder of an electron generating substance that generates electrons by using alpha rays released from the natural mineral, and a fluidity binder to form a fluid substance activation raw material.

[0062] The substance activation component filling step S22 is a process of filling the fluid substance activation raw material into the inside of a cylindrical magnet having an N pole at one end and an S pole at the other end. By completing this process, the substance activation component is completed. As long as the magnet is cylindrical, its outer shape is not particularly limited, and various shaped magnets such as a cylindrical shape and a polygonal cylindrical shape can be used.

[0063] Here, as the fluidity binder used in the substance activation raw material forming step S21, it is more preferably to use a fluidity binder having conductivity. In addition, as the fluidity binder, it can be dry, or it can also be non-dry. In the case of using a dry fluidity binder, it is particularly preferable to use a normal temperature plating solution containing zinc. In addition, in the case of using a dry fluidity binder, as a subsequent process to the substance activation component filling step S22, it is preferable to provide a drying step, which is a process of drying the substance activation raw material put into the cylindrical magnet. In this drying step, the substance activation raw material can be dried by natural drying, or it can also be dried by heating.

[0064] According to the second manufacturing method of such a substance activation component, a substance activation component that can greatly exert a greater activation effect of the substance can be easily manufactured.

[0065] In addition, by connecting the electrode part to the substance activation component manufactured in this way, the electrons generated by the substance activation component can be efficiently transferred to the substance to be activated. The raw material for forming the electrode part is not particularly limited. For example, raw materials with high conductivity such as copper, silver, and gold are preferably used, and copper is more preferably used from the aspect of cost. In addition, the connection method between the substance activation component and the electrode part is not particularly limited. For example, it can be connected by a conductive adhesive, or the substance activation component can be simply placed on the plate-shaped electrode part and the two can be brought into contact for connection.

[0066] In addition, if the electrode part is configured to be connected to a magnet, there is no particular limitation. It is preferable that the electrode part is connected to one end of the cylindrical magnet on the N-pole side. In particular, as Figure 3 the schematic cross-sectional view of the configuration, and as the top view observed from the arrow A direction of Figure 3 shown, it is particularly preferable to be configured as a plate-shaped electrode 2 that is connected to the entire area of the end face of one end of the magnet 1 on the N-pole side and closes the opening on one end side of the cylindrical magnet 1. In addition, more preferably, the plate-shaped electrode 2 is formed to have an area larger than the area surrounded by the outer peripheral contour line of one end of the cylindrical magnet. Figure 4 In this way, in the substance activation component formed by filling the substance activation raw material into the inside of the cylindrical magnet 1, since the electrons generated in the substance activation raw material use the magnetic field lines of the magnet 1 to increase the moving speed of the electrons, and the moving direction of the electrons is controlled by the magnetic field lines, the electrons can be transferred to the substance to be activated at high speed.

[0067] In addition, as

[0068] shown, the magnetic field lines of the magnet come out from the N-pole side and enter the S-pole side. Therefore, the configuration that the electrode part is connected to one end on the N-pole side can efficiently guide the generated electrons to the electrode part and transfer them to the substance to be activated. In particular, as Figure 5 shown, from the viewpoint of efficiently transferring the electrons generated in the substance activation raw material filled inside the cylindrical magnet to the substance to be activated, it is preferable to adopt the plate-shaped electrode 2 that is connected to the entire area of the end face of one end of the magnet 1 on the N-pole side. In addition, by forming the plate-shaped electrode 2 to have an area larger than the area surrounded by the outer peripheral contour line of one end of the cylindrical magnet 1, the electrons moving along the magnetic field lines formed outside the magnet 1 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 1 can be efficiently transferred to the substance to be activated. Figure 3 、 Figure 4 shown. In addition, by forming the plate-shaped electrode 2 to have an area larger than the area surrounded by the outer peripheral contour line of one end of the cylindrical magnet 1, the electrons moving along the magnetic field lines formed outside the magnet 1 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 1 can be efficiently transferred to the substance to be activated.

[0069] In addition, asFigure 6 As shown in the schematic cross-sectional view of the configuration, the second manufacturing method can also be configured to include a step of covering the side surface portion and the other end portion side of the magnet 1 with an insulating member 3. The raw material for forming the insulating member 3 is not particularly limited, and generally known insulating raw materials can be used. In addition, the insulating member 3 can be a detachable member such as a rubber cover, or the surface of the magnet 1 can be covered and fixed with an insulating resin raw material so that it cannot be detached. By providing such an insulating member 3, it is possible to effectively prevent electrons generated from the material activation raw material filled inside the cylindrical magnet 1 from being released to the outside of the material activation member, and the generated electrons can be effectively transmitted to the material activation target.

[0070] In addition, as needed, it can also be configured to include a compression step of compressing the material activation raw material filled into the inside of the cylindrical magnet 1 after filling the material activation raw material into the inside of the cylindrical magnet 1 in the material activation member filling step S22. In this compression step, various conventionally known pressure devices can be used for implementation. In addition, when configured to include a compression step, in the case where a dry flowable binder is used as the material activation raw material and a drying step, that is, a step of drying the material activation raw material input into the cylindrical magnet 1, is provided as a subsequent step to the material activation member filling step S22, it is preferable that the material activation raw material in the cylindrical magnet 1 in this drying step is not completely dried, but is semi-dried to such an extent that it can be deformed during compression.

[0071] Furthermore, a third manufacturing method of the material activation member according to the present invention will be described. 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. This third manufacturing method of the material activation member is also a manufacturing method of a material activation member that can effectively transmit the generated electrons to the material activation target using magnetic field lines, as Figure 7 shown in the block diagram, includes a material activation raw material forming step S31, a charging into the mold step S32, a drying step S33, and a magnetization step S34.

[0072] The material activation raw material forming step S31 is a process of mixing and stirring the powder of the above-mentioned natural mineral containing a radioactive substance, the powder of an electron generating substance that generates electrons using alpha rays released from the natural mineral, the powder of a ferrite magnet raw material, and a dry flowable binder to form a flowable material activation raw material.

[0073] Here, as the flowable binder used in the material activation raw material forming step S31, it is more preferable to use a conductive flowable binder. As a dry conductive flowable binder, it is particularly preferable to use a room temperature plating solution containing zinc.

[0074] The input type box step S32 is a process of putting a fluidic material activation raw material into a mold box with a specified shape. There are no particular limitations on the shape of the mold box, etc., and various mold boxes can be used.

[0075] The drying step S33 is a process of drying the material activation raw material put into the mold box. In this drying step S13, the material activation raw material can be dried by natural drying, or the material activation raw material can also be dried by heating.

[0076] The magnetization step S34 is a process of magnetizing the dried material activation raw material. The method of magnetization is not particularly limited, and known methods in the past can be adopted. In addition, it is preferable to magnetize after taking out the dried material activation part from the mold box.

[0077] In addition, if necessary, it can also be configured to include a compression step of compression molding the material activation raw material put into the mold box as a process between the drying step S33 and the magnetization step 34. In this compression step, various known pressure devices can be used for implementation. In addition, when configured to include a compression step, it is preferable that the material activation raw material in the mold box in the above drying step S33 is not completely dried, but is semi-dried to the extent that it can be deformed during compression.

[0078] By completing the magnetization step S34, the material activation part is completed. In addition, by connecting the above electrode part to this material activation part, the electrons generated by the material activation part can be efficiently transmitted to the material activation object.

[0079] Similar to the material activation part manufactured by the above second manufacturing method, the electrons generated by the material activation part manufactured in this way use magnetic field lines to increase the moving speed of the electrons, and in addition, use magnetic field lines to control the moving direction of the electrons. Therefore, the electrons can be transmitted to the material activation object at high speed, and a material activation part that can greatly exert a greater material activation effect can be manufactured very simply in various forms.

[0080] Finally, the fourth manufacturing method of the manufacturing method of the material activation part 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, it can be implemented with appropriate modifications. As Figure 8 As shown in the block diagram shown, the third manufacturing method of this material activation part includes a material activation raw material forming step S41, an input mold box step S42, and a compression molding step S43.

[0081] The step S41 of forming the material activation raw material is a process of mixing the powder of the natural mineral containing the radioactive substance and the powder of the electron generation substance that generates electrons by using the alpha rays released from the natural mineral to form the material activation raw material.

[0082] The step S42 of charging into the mold box is a process of charging the material activation raw material mixed in the step S41 of forming the material activation raw material into a mold box with a specified shape. There is no particular limitation on the shape of the mold box, and various shapes can be used. Preferably, it has a shape that can efficiently perform the compression process in the compression forming step performed in the subsequent process.

[0083] The compression molding step S43 is a process of compressing the material activation raw material charged into the mold box to solidify and mold it into a specified shape. In this compression molding step S43, various conventionally known pressure devices can be used.

[0084] After the compression molding step S43 is completed, the compression-molded material activation raw material is taken out from the mold box, and the material activation component is completed. In addition, by connecting the electrode part to this material activation component, the electrons generated by the material activation component can be efficiently transmitted to the material activation object.

[0085] According to the fourth manufacturing method of such a material activation component, a material activation component that can exhibit a greater activation effect of the material can be manufactured extremely simply in various forms.

[0086] The material activation component manufactured by the above manufacturing method is installed in a device in which the material to be activated exists inside in various fields, so that the material can be effectively activated. For example, a sheet-like material activation component 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 material activation component are transmitted 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 material activation component is installed outside the air duct, it does not become a resistance when the engine intakes air.

[0087] In addition, by winding the substance activation component around the outer side of the exhaust pipe of an automobile, electrons released from the substance activation component are transferred to compounds such as carbon monoxide, carbon dioxide, and nitrogen oxides contained in the exhaust gas, which can greatly promote the activation of these compounds. These compounds are sent to the catalyst device in a state where they are greatly activated by the transferred electrons, so purification can be carried out very efficiently. In addition, since the substance activation component is wound around the outer side of the exhaust pipe of the automobile, this component will not be damaged by the influence of high-temperature exhaust gas.

[0088] In addition, by winding the substance activation component around the outer side of the cylinder block of an automobile, electrons released from the substance activation component act on the intake air or exhaust gas of the automobile engine flowing through the inside of the cylinder block, which can greatly promote their activation. 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 very efficiently.

[0089] In addition, the substance activation component 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 of the parts where metals of the machine slide against each other, lubricating oil is used. However, 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 in such a way as to be on the outer side of the container for storing the lubricating oil for lubricating the sliding parts of the machine or the pipe through which the lubricating oil flows, electrons radiated from the substance activation component act on the lubricating oil flowing through the inside of the lubricating device, greatly promoting the activation of the lubricating oil. 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.

[0090] In addition, the material activation component 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 around the container that stores the coolant that cools the heat-generating part of the machine or the outside of the pipe in which the coolant flows, the electrons emitted from the material activation component act on the coolant flowing through the inside of the cooling device, greatly promoting the activation of the coolant. Thus, 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 thus 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 of the pump can be reduced, 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.

[0091] In addition, the material activation component 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 around the outside of a container that stores the liquid fuel or gaseous fuel supplied to the internal combustion engine or a pipeline that flows through these fuels inside, the electrons generated from the material activation component 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.

[0092] In addition, the substance activation component can also be used to form the moving blades of a turbine. By causing working fluids such as water in hydroelectric power generation, steam in thermal power generation, and oil in an automotive automatic transmission to act on the turbine blades respectively, rotational driving force is 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 too high, the energy transfer ability from the fluid to the turbine blades will be reduced. Thus, by winding the substance activation component around the outer side of the turbine blades or the outer side of the housing that houses the turbine blades inside, the electrons generated from the substance activation component 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, enabling the fluid to flow 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.

[0093] In addition, the substance activation component 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 the refrigerator, 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 around the evaporator, which is the passage for the refrigerant in the cooling device, or on the pipeline through which the refrigerant flows inside, the electrons generated from the substance activation component 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.

[0094] In addition, the substance activation component can also be used for the 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 consuming a large amount of electricity and fuel costs. Thus, by winding the substance activation component around the cleaning water storage container or the pipeline through which the cleaning water flows, the electrons generated from the substance activation component act on the fluid, greatly promoting the activation of the cleaning water. If the tap water activated by the transferred electrons is used as the solvent, 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 activated by the transferred electrons also has the effect of preventing corrosion inside the water pipes.

[0095] In addition, the substance activation component 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 water, but in this method, the absorption amount of water absorbed by the roots of the plants can only 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 around the water supply container containing the water supplied to the plants and containing nutrients or on the pipeline through which the supply water flows inside, the electrons generated from the substance activation component 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 water and nutrients thus activated can be easily absorbed by the root hairs of the plants, so that 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 sufficiently dissolved with nitrogen compounds.

[0096] In addition, the substance activation component 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 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 act on the supply water to activate it. The activated water is easily absorbed into the bodies of the 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.

[0097] In addition, the substance activation component 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 water is very important. When raising fish and shellfish, excreta are discharged into the same water tank as the living water. Therefore, if it is not purified regularly, the water quality will deteriorate. Therefore, by winding the substance activation component around the water supply container for the water supplied to fish and shellfish, the circulation 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 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.

[0098] In addition, the substance activation component 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 around the air supply pump for ventilation or the outer side of a pipeline through which ventilation air flows inside, the electrons generated from the substance activation component act on the air passing through the pump or the air flowing through the pipeline to activate 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.

[0099] In addition, the substance activation component 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 atomize paint by using air as it is, so it is difficult to further reduce the particle size of the atomized paint. Therefore, by winding the substance activation component around the compressed air supply pump for spraying paint and atomizing the paint or the outer side of a pipeline through which compressed air flows inside, the electrons generated from the substance activation component act on the air passing through the pump or the air flowing through the pipeline to activate the air, and the activated compressed air is used 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.

[0100] In addition, it has been confirmed that by making the electrons released from the substance activation component act on a fluid (gas, liquid, powder) moving in a pipeline, the flow rate of the fluid is increased and the transfer efficiency is improved. For example, the time taken for transferring powder from a tanker truck to a tank at a factory through a pipeline can be shortened. This can be considered to be due to the fact that by imparting electrons, static electricity is removed, and the frictional resistance between the powder and the pipeline is reduced, thereby increasing the flow rate. In addition, by winding the substance activation component around the outer side of the exhaust pipe of an automobile, etc., electrons are imparted to the exhaust gas, so that the discharge speed of the exhaust gas is also increased, and the passage of the exhaust gas through the exhaust pipe is improved. As a result, the combustion efficiency of the engine is also increased.

[0101] Since the inventor conducted an experiment to confirm the effects of the substance activation component of the present invention, the following description will be given. First, a substance activation component for experimental use was fabricated into Figure 9The shape shown in the figure 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) constituting the material activation raw material, the powder of the electron generating material, the room temperature plating solution containing zinc (a fluid binder with conductivity; a room temperature electroplating paint containing 96% zinc), and the copper powder for improving conductivity are mixed and stirred thoroughly, poured into a mold, and taken out from the mold after drying. Electrodes composed of copper with a thickness of 0.02 mm (length × width = 40 mm × 60 mm) are laminated on both sides to form the material activation component. In addition, a wire is connected to the copper electrode parts arranged on both sides of the material activation component, and a plate-shaped terminal part is connected to the front end thereof, so that the electrons generated in the material activation component 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 20.8 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, and lanthanum hexaboride 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. The content of copper powder used to improve conductivity is 1.5 parts by mass relative to 100 parts by mass of the material activation raw material.

[0102] like Figure 10As 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 is 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 lubrication effect, the noise level was also reduced. According to these phenomena, it is expected that electricity can be saved by managing the set temperature. In addition, for all electrical products, by applying electricity to the equipment, the thermal conductivity is increased, the current is improved, and thus the efficiency is increased. Utilizing the effect of reducing frictional resistance helps to save electricity costs. 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 is also increased.

[0103] 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 the static electricity is removed by the substance activation component, thereby being able to cut off the cycle in which static electricity is generated due to the rotation of the resin blades and the friction with the air, and due to the 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 was reduced.

[0104] In addition, it was confirmed that by imparting electrons released from the substance activation component 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 (the passage of heating time) during heating under the same conditions was measured. The measurement results are shown in Table 1 below. Figure 11 The figure showing the measurement results. From these Table 1, Figure 11 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 to 60 °C is increased by nearly 40% compared to water without electrons imparted. Thus, due to the increase in the thermal conductivity of water, the penetration power increases, the extraction power of the cooked food increases, and it can also 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. In addition, after stirring oil into water, when the separation state was confirmed in ordinary water and electron-supplied water, the separation occurred faster on the side of ordinary water. Therefore, it was also confirmed that the affinity between electron-supplied water and oil increases.

[0105] [Table 1] In addition, it was confirmed that if electrons released from the substance activation component are imparted to a cutting machine for metal processing, the cutting proceeds more smoothly and the cutting accuracy of the processed surface improves. 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 the metals from directly contacting each other to reduce friction. However, it was confirmed that instead of this lubricating oil, by imparting electrons, even when the metals are in contact with each other, sintering is difficult to occur due to the reduction of frictional resistance.

[0106] 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 when fully charged, it can only be charged to 80% of the power. However, by adding a few mL of an organic germanium solution supplied with electrons released from the substance activation component to each cell of the battery, even if the battery capacity has decreased to 80%, as long as normal operation is carried out for a few days, the maximum capacity of the battery can be restored to 100%. In addition, 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%. In addition, it was also confirmed that: when charging the lithium-ion battery, if electrons are added from the negative terminal via the substance activation component, the capacity of the battery that has become old and decreased also gradually increases.

[0107] In addition, the following two batteries were prepared as automotive batteries, and a battery recovery test was conducted. Battery 1: The battery that was replaced due to battery depletion and then placed Battery 2: The battery that could be used without problems In addition, Battery 1 had an open-circuit voltage of 8.8V, 5V when the charger was connected, was lower than the reference 7.4V, and was a battery that could not be restored by charging. Battery 2 had an open-circuit voltage of 12.2V and had no problems with normal charging.

[0108] For these Battery 1 and Battery 2, battery fluid supplied with electrons was injected to the specified electrolyte level (5 cc per unit), and charging was performed. Battery 1 was in a state where the charger circuit did not operate and could not be charged. Battery 2 was fully charged after 7 hours of normal charging. Since Battery 1 had been left in a depleted state for half a year, it was in a non-renewable state where the electrodes were sulfated and crystallized and no current flowed at all. Therefore, Battery 2 was connected in parallel with Battery 1, the voltage was raised above 10V at which the charger operates, and the charging circuit was made to operate. Immediately afterwards, Battery 2 was 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 it became possible to charge. After 5 hours, at the moment when charging was about 40% complete, foam blew out from the cover of the electrolyte and the internal electrolyte overflowed. Overall, nearly 20 cc overflowed. Before the battery fluid supplied with electrons was put in, 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.

[0109] 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 any problems. Additionally, it is said that sulfates in a battery that usually causes over-discharge (a state where the battery is depleted and drops to 10 V) cover the electrodes, and it is impossible to fully recover even with charging. Moreover, for a battery that has dropped below 7.4 V, 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 with the electrodes covered by 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 recovered without any problems. Additionally, one week after the above test, a battery installation test was conducted. With the air conditioner turned on all the time, there were no problems even during about half-day operation each of day and night. The engine starting condition was also very good, and there was no dimming effect of the headlamps felt at all when idling.

[0110] In addition, using a DELICA D5 manufactured by Mitsubishi Motors Corporation, the change in engine sound during hill 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. Figure 12 And Figure 13 show the measurement results. Additionally, Figure 12 shows the measurement results in the case of not installing the substance activation component on the engine, Figure 13 shows the measurement results in the case of installing the substance activation component on the engine. 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. Additionally, Figure 14 And Figure 15 show the measurement results related to the frequency distribution. Additionally, Figure 14 shows the measurement results in the case of not installing the substance activation component on the engine, and Figure 15 shows the measurement results in the case of installing the substance activation component on the engine. From these Figure 14 , Figure 15 it can be confirmed that the engine sound at low frequencies below 150 Hz decreased.

[0111] In addition, it was confirmed that: when electrons are imparted during the incubation of chicken eggs, the utilization rate of the egg yolk during incubation is approximately close to 100%. If a blood test is performed on the chicks, the mRNA value of the spleen immune index increases, and the body weight also increases compared to the standard value. It is considered that the impact on the sheep hemagglutination antibody titer of chicks 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 electrons are imparted to the ankle, the blood flow rate at the tips of the toes increases within just 10 seconds, and it was confirmed that the surface temperature of the back of the hand rises by 2 - 4°C on average within several tens of minutes.

[0112] In addition, 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, four types of non-drying substance activation raw materials for experimental use (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.

[0113] [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. In addition, 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. In addition, the average particle size of the titanium dioxide powder, metal silicon powder, black silicon dioxide powder, copper powder, lanthanum hexaboride (LaB6) powder, gallium nitride (GaN) powder, and tourmaline powder is 1 μm or less.

[0114] The non-drying substance activation raw materials of the above samples were coated on the capacitors and transistors of an audio device (manufactured by DENON: CD player: DCD-1650AR). 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. In addition, a sensory test was also conducted under the condition of not coating the non-drying substance activation raw materials. As a result, compared with the case of not coating the non-drying substance activation raw materials, the following evaluations were obtained for the case of coating the non-drying substance activation raw materials of each sample: the transparency of the sound increased, and in addition, it was full of a sense of presence and sounded vivid. This is considered to be the effect obtained by the electrons released from the non-drying substance activation raw materials and transmitted to the audio device reducing the mechanical noise emitted from the audio device and the noise coming around from the power supply.

[0115] In addition, compared with the case of coating sample 1, in the case of coating sample 2, the result of further increasing the transparency of the sound and the like was obtained. This is considered to be the effect obtained by increasing the content of titanium dioxide and containing gallium nitride. In addition, compared with the case of coating sample 2, in the case of coating sample 3, the result of better sound quality, increased transparency of the sound, and increased sense of presence was obtained. This is considered to largely reflect the effect brought about by the increase in the content of molybdenum disulfide powder in the molybdenum disulfide slurry and the further improvement of conductivity. In addition, it is considered to be the effect obtained by containing the powder of lanthanum hexaboride. Furthermore, compared with the case of coating sample 3, in the case of coating sample 4, 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. This is considered to be the effect of increasing the content of titanium dioxide.

[0116] In addition, the inventor coated the non-drying substance activation raw materials of the above samples 1 to 4 on the power-related device of a milling machine that rotates a cutter to cut metal and the like, and confirmed whether the machining accuracy changed and whether the mechanical operation sound changed. As a result, compared with the case of not coating, for the case of coating the non-drying substance activation raw materials of each sample, it was confirmed that the machining accuracy was improved, and in addition, the mechanical operation sound became quieter. This is considered to be the effect obtained by the action of the electrons released from the non-drying substance activation raw materials and transmitted to the milling machine, the reduction of the frictional resistance between the cutter and the workpiece, and as a result, the reduction of the vibration of the rotating cutter. In addition, it was confirmed that: compared with sample 1, the above effect was greater for sample 2, and in addition, compared with sample 2, the above effect was greater for sample 3, and furthermore, it was confirmed that: compared with sample 3, sample 4 showed a greater above effect.

[0117] 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. The non-drying substance activation raw material of Sample 1 was coated on the fixed capacitors of the motherboard. As a result of this confirmation test, it was confirmed that the startup time was 25 seconds before coating, while it changed to 15 seconds after coating. In addition, the coating position of the non-drying substance activation raw material for the fixed capacitors 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 memory of this personal computer, an improvement in quietness and perceived speed was confirmed. From this result, it was found that the electronic generation paste according to the present invention can improve the operation speed and quietness of the computer. Description of reference numerals:

[0118] S11: Substance activation raw material formation step; S12: Input into the mold box step; S13: Drying step; S21: Substance activation raw material formation step; S22: Substance activation component filling step; S31: Substance activation raw material formation step; S32: Input into the mold box step; S33: Drying step; S34: Magnetization step; S41: Substance activation raw material formation step; S42: Input into the mold box step; S43: Compression molding step; 1: Magnet; 2: Electrode part; 3: Insulating component.

Claims

1. A method for producing a material for material activation, characterized in that: A material activation raw material having fluidity is formed by mixing and stirring a powder of a natural mineral containing a radioactive substance, a powder of an electron generating substance that generates electrons by utilizing alpha rays emitted from the natural mineral, and a dry fluid binder.

2. A method for producing a material for material activation, characterized in that: A material activation raw material having fluidity is formed by mixing and stirring a powder of a natural mineral containing a radioactive substance, a powder of an electron generating substance that generates electrons by utilizing alpha rays emitted from the natural mineral, and a non-drying fluid binder.

3. The method for producing a material for material activation according to claim 1 or 2, 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.

4. The method for producing a material for material activation 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.

5. The method for producing a material for material activation according to claim 1, characterized in that: The fluid adhesive has electrical conductivity.

6. The method for manufacturing a material activating component according to claim 5, characterized in that: The fluid binder comprises powder of at least one selected from the group consisting of zinc, molybdenum disulfide and copper.

7. The method for manufacturing a material activating component according to claim 5, characterized in that: The fluid adhesive is a room temperature plating solution containing zinc.

8. The method for producing a material for material activation according to claim 2, characterized in that: The fluid adhesive has electrical conductivity.

9. The method for producing a material for material activation according to claim 8, characterized in that: The fluid binder comprises powder of at least one selected from the group consisting of zinc, molybdenum disulfide and copper.

10. The method for producing a material for material activation according to claim 8, characterized in that: The fluid adhesive is molybdenum disulfide grease or copper grease.

11. A method for manufacturing a material activation component, characterized in that: include: a material activation raw material forming step of mixing and stirring powder of a natural mineral containing a radioactive substance, powder of an electron generating substance that generates electrons by utilizing alpha rays emitted from the natural mineral, and a dry fluid binder to form a material activation raw material having fluidity; A step of placing the fluid material activating raw material into a mold box; and The drying step is to dry the active raw material of the substance put into the mold.

12. A method for manufacturing a material activation component, characterized in that: include: a material activation raw material forming step of mixing and stirring powder of a natural mineral containing a radioactive substance, powder of an electron generating substance that generates electrons by utilizing alpha rays released from the natural mineral, and a fluid binder to form a material activation raw material having fluidity; as well as The material activation component filling step is to fill the material activation raw material having fluidity into the interior of a cylindrical magnet having an N pole at one end and an S pole at the other end.

13. A method for manufacturing a material activation component, characterized in that: include: a material activation raw material forming step of mixing and stirring powder of a natural mineral containing a radioactive substance, powder of an electron generating substance that generates electrons by utilizing alpha rays emitted from the natural mineral, powder of a ferrite magnet raw material, and a dry fluid binder to form a material activation raw material having fluidity; A step of placing the material activation raw material having fluidity into a mold box; A drying step, drying the active raw material of the substance put into the molding box; as well as The magnetization step is to magnetize the dried active raw material of the substance.

14. The method for manufacturing a material activating component according to any one of claims 11 to 13, 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.

15. The method for manufacturing a material activating component according to any one of claims 11 to 13, 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.

16. The method for manufacturing a material activating component according to any one of claims 11 to 13, characterized in that: The fluid adhesive has electrical conductivity.

17. The method for manufacturing a material activating component according to claim 16, characterized in that: The fluid binder comprises powder of at least one selected from the group consisting of zinc, molybdenum disulfide and copper.

18. The method for manufacturing a material activating component according to any one of claims 11 to 13, characterized in that: The fluid adhesive is a room temperature plating solution containing zinc.

19. A method for manufacturing a material activation component, characterized in that: include: a material activation raw material forming step of mixing powder of a natural mineral containing a radioactive substance and powder of an electron generating substance that generates electrons by utilizing alpha rays emitted from the natural mineral to form a material activation raw material; A step of placing the material activation raw material into a mold box; and The compression molding step is to compression mold the material activation raw material put into the mold box.

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