WO2015151420A1 - アトマイズ金属粉末の製造方法 - Google Patents
アトマイズ金属粉末の製造方法 Download PDFInfo
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- WO2015151420A1 WO2015151420A1 PCT/JP2015/001407 JP2015001407W WO2015151420A1 WO 2015151420 A1 WO2015151420 A1 WO 2015151420A1 JP 2015001407 W JP2015001407 W JP 2015001407W WO 2015151420 A1 WO2015151420 A1 WO 2015151420A1
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
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- B22F9/00—Making metallic powder or suspensions thereof
- B22F9/02—Making metallic powder or suspensions thereof using physical processes
- B22F9/06—Making metallic powder or suspensions thereof using physical processes starting from liquid material
- B22F9/08—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying
- B22F9/082—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying atomising using a fluid
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F9/00—Making metallic powder or suspensions thereof
- B22F9/002—Making metallic powder or suspensions thereof amorphous or microcrystalline
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C33/00—Making ferrous alloys
- C22C33/02—Making ferrous alloys by powder metallurgy
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C33/00—Making ferrous alloys
- C22C33/02—Making ferrous alloys by powder metallurgy
- C22C33/0257—Making ferrous alloys by powder metallurgy characterised by the range of the alloying elements
- C22C33/0264—Making ferrous alloys by powder metallurgy characterised by the range of the alloying elements the maximum content of each alloying element not exceeding 5%
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C45/00—Amorphous alloys
- C22C45/02—Amorphous alloys with iron as the major constituent
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F9/00—Making metallic powder or suspensions thereof
- B22F9/02—Making metallic powder or suspensions thereof using physical processes
- B22F9/06—Making metallic powder or suspensions thereof using physical processes starting from liquid material
- B22F9/08—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying
- B22F9/082—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying atomising using a fluid
- B22F2009/0824—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying atomising using a fluid with a specific atomising fluid
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F9/00—Making metallic powder or suspensions thereof
- B22F9/02—Making metallic powder or suspensions thereof using physical processes
- B22F9/06—Making metallic powder or suspensions thereof using physical processes starting from liquid material
- B22F9/08—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying
- B22F9/082—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying atomising using a fluid
- B22F2009/0824—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying atomising using a fluid with a specific atomising fluid
- B22F2009/0828—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying atomising using a fluid with a specific atomising fluid with water
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F9/00—Making metallic powder or suspensions thereof
- B22F9/02—Making metallic powder or suspensions thereof using physical processes
- B22F9/06—Making metallic powder or suspensions thereof using physical processes starting from liquid material
- B22F9/08—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying
- B22F9/082—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying atomising using a fluid
- B22F2009/0848—Melting process before atomisation
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F9/00—Making metallic powder or suspensions thereof
- B22F9/02—Making metallic powder or suspensions thereof using physical processes
- B22F9/06—Making metallic powder or suspensions thereof using physical processes starting from liquid material
- B22F9/08—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying
- B22F9/082—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying atomising using a fluid
- B22F2009/086—Cooling after atomisation
- B22F2009/0872—Cooling after atomisation by water
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F9/00—Making metallic powder or suspensions thereof
- B22F9/02—Making metallic powder or suspensions thereof using physical processes
- B22F9/06—Making metallic powder or suspensions thereof using physical processes starting from liquid material
- B22F9/08—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying
- B22F9/082—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying atomising using a fluid
- B22F2009/0888—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying atomising using a fluid casting construction of the melt process, apparatus, intermediate reservoir, e.g. tundish, devices for temperature control
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F2301/00—Metallic composition of the powder or its coating
- B22F2301/35—Iron
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F2998/00—Supplementary information concerning processes or compositions relating to powder metallurgy
- B22F2998/10—Processes characterised by the sequence of their steps
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F2999/00—Aspects linked to processes or compositions used in powder metallurgy
Definitions
- the present invention relates to a method for producing metal powder (hereinafter also referred to as atomized metal powder) using an atomizer, and more particularly to a method for improving the cooling rate of metal powder after atomization.
- the atomizing method includes a water atomizing method in which a metal powder is obtained by injecting a high-pressure water jet into a molten metal flow, and a gas atomizing method in which an inert gas is injected in place of the water jet.
- the flow of molten metal is divided by a water jet sprayed from a nozzle to form a powdered metal (metal powder), and the powdered metal (metal powder) is also cooled by a water jet. Metal powder is obtained.
- the flow of molten metal is divided by an inert gas injected from a nozzle to form a powdered metal (metal powder), and then the powdered metal (metal powder) is usually placed under the atomizer.
- the metal powder is dropped into a water tank or a drum of running water, and the powdered metal (metal powder) is cooled to obtain an atomized metal powder.
- Patent Document 1 describes a method for producing a metal powder in which the cooling rate until solidification is 10 5 K / s or more when a metal powder is obtained by cooling and solidifying while scattering molten metal. .
- the above-described cooling rate is obtained by bringing the scattered molten metal into contact with the coolant flow generated by swirling the coolant along the inner wall surface of the cylindrical body. It is supposed to be done.
- the flow rate of the coolant flow generated by swirling the coolant is preferably 5 to 100 m / s.
- Patent Document 2 describes a method for producing rapidly solidified metal powder.
- the cooling liquid is supplied from the outer peripheral side of the upper end of the cylindrical portion of the cooling container whose inner peripheral surface is a cylindrical surface, and is allowed to flow down while swirling along the inner peripheral surface of the cylindrical portion, A layered swirl cooling liquid layer having a cavity at the center is formed by the centrifugal force generated by the swirl, and a molten metal is supplied to the inner peripheral surface of the swirl cooling liquid layer to rapidly cool and solidify.
- the cooling efficiency is good and a high-quality rapidly solidified powder can be obtained.
- Patent Document 3 discloses a gas jet nozzle for injecting a gas jet onto a flowing molten metal to divide it into droplets, and a cooling cylinder having a cooling liquid layer flowing down while turning to the inner peripheral surface.
- An apparatus for producing metal powder by a gas atomizing method is provided. According to the technique described in Patent Document 3, the molten metal is divided into two stages by a gas jet nozzle and a swirling cooling liquid layer, and a finely cooled rapidly solidified metal powder is obtained.
- Patent Document 4 molten metal is supplied into a liquid refrigerant, a vapor film that covers the molten metal is formed in the refrigerant, and the resulting vapor film is collapsed so that the molten metal and the refrigerant are in direct contact with each other.
- a method for producing amorphous metal fine particles is described in which boiling due to natural nucleation is generated and the molten metal is rapidly cooled and amorphized by using the pressure wave to form amorphous metal fine particles.
- the collapse of the vapor film covering the molten metal can be achieved by bringing the temperature of the molten metal supplied to the refrigerant into direct contact with the refrigerant so that the interface temperature is lower than the film boiling lower limit temperature and higher than the spontaneous nucleation temperature or is irradiated with ultrasonic waves. Or that is possible.
- Patent Document 5 when the molten material is supplied as a droplet or a jet flow into the liquid refrigerant, the temperature of the molten material is directly brought into contact with the liquid refrigerant. It is set so that it is in a molten state above the generation temperature, and the relative speed difference between the speed of the molten material and the speed of the liquid refrigerant when entering the liquid refrigerant flow is 10 m / s or more.
- Patent Document 6 a raw material obtained by adding a functional additive to a base material is melted and supplied into a liquid refrigerant so that it is refined by vapor explosion and cooled at the time of solidification by cooling.
- the step of obtaining homogeneous functional fine particles that are polycrystalline or amorphous without segregation by controlling the amount of the particles, and the step of obtaining functional members by solidifying the functional fine particles and the fine particles of the base material as raw materials The manufacturing method of the functional member which comprises these is described.
- JP 2010-150587 A Japanese Examined Patent Publication No. 7-107167 Japanese Patent No. 3932573 Japanese Patent No. 3461344 Japanese Patent No. 4793872 Japanese Patent No. 4784990
- Patent Documents 1 to 3 try to peel off the vapor film formed around the metal particles by supplying the molten metal divided into the cooling liquid layer formed by swirling the cooling liquid.
- the cooling liquid layer tends to be in a film boiling state, and the metal particles supplied into the cooling liquid layer move together with the cooling liquid layer. There is a problem that it is difficult to avoid the film boiling state.
- the vapor film covering the molten metal is collapsed by using a steam explosion that is chain-boiled to a nucleate-boiling state, thereby reducing the size of the metal particles. Furthermore, it intends to make it amorphous. It is an effective method to remove the vapor film of the film boiling using the vapor explosion.
- the boiling curve shown in FIG. 4 is used. As can be seen, at least first, it is necessary to cool the surface temperature of the metal particles to below the MHF (Minimum Heat Flux) point.
- MHF Minimum Heat Flux
- FIG. 4 is an explanatory diagram schematically showing a relationship between the cooling ability and the surface temperature of the material to be cooled when the refrigerant is water (cooling water), which is called a boiling curve.
- the refrigerant is water (cooling water), which is called a boiling curve.
- the cooling to the MHF point temperature is cooling in the film boiling region, and in the cooling in the film boiling region, a vapor film is formed between the surface to be cooled and the cooling water. Therefore, weak cooling is performed. For this reason, when cooling is started from the MHF point or higher for the purpose of making the metal powder amorphous, there is a problem that the cooling rate for making amorphous becomes insufficient.
- An object of the present invention is to solve the problems of the prior art and to provide a method for producing atomized metal powder, which can rapidly cool metal powder and can be used as amorphous metal powder.
- the present inventors first made extensive studies on various factors affecting the MHF point in water jet cooling. As a result, it has been found that the influence of the temperature and the injection pressure of the cooling water is large.
- SUS304 stainless steel plate (size: 20 mm thickness x 150 mm width x 150 mm length) was used as the material.
- a thermocouple was inserted into the material from the back surface, and the temperature at a position 1 mm (width center, length center) from the surface could be measured.
- the material was charged into an oxygen-free atmosphere heating furnace and heated to 1200 ° C. or higher.
- the heated material was taken out, and immediately, cooling water was sprayed onto the material from the atomizing cooling nozzle while changing the water temperature and the injection pressure, and the temperature change at a position of 1 mm from the surface was measured. From the temperature data obtained, the cooling capacity during cooling was estimated by calculation. A boiling curve was created from the obtained cooling capacity, and the MHF point was determined by judging that the point where the cooling capacity suddenly increased was the point where film boiling changed to transition boiling.
- the MHF point when cooling water having a water temperature of 30 ° C. used in a normal water atomizing method is injected at an injection pressure of 1 MPa, the MHF point is about 700 ° C. while the cooling water is being injected.
- the MHF point when cooling water having a water temperature of 10 ° C. or less and 2 ° C. or more is injected at an injection pressure of 5 MPa or more and 20 MPa or less, the MHF point is 1000 ° C. or more in a state where the cooling water is being injected. That is, when the cooling water temperature (water temperature) is lowered to 10 ° C. or lower and the injection pressure is increased to 5 MPa or higher, the MHF point rises and the temperature at which film boiling changes to transition boiling becomes high. I found it.
- the temperature of the metal powder after atomizing the molten metal has a surface temperature of about 1000 to 1300 ° C, and the necessary cooling temperature range for preventing crystallization is from about 1000 ° C to the first crystallization. It is necessary to cool the temperature range to below the temperature, and when the water injection cooling is started at a temperature at which the metal powder cooling start temperature is higher than the MHF point, the cooling of the film boiling region having a low cooling capacity is performed at the start of cooling. From this, it is possible to start the cooling of the metal powder at least from the transition boiling region if the cooling is started by water jet cooling such that the MHF point is equal to or higher than the necessary cooling temperature range, compared with the film boiling region.
- Cooling is promoted, and the cooling rate of the metal powder can be remarkably increased. It has been found that if the metal powder is cooled with such a high cooling capacity, rapid cooling in the crystallization temperature range essential for amorphization of the metal powder can be realized easily.
- the present invention has been completed based on such findings and further studies. That is, the gist of the present invention is as follows. (1) A method for producing an atomized metal powder in which a fluid is jetted into a molten metal stream, the molten metal stream is divided into a metal powder, and the metal powder is cooled. Hereinafter, the method for producing atomized metal powder, wherein the molten metal flow is divided and the metal powder is cooled as spray water having an injection pressure of 5 MPa or more. (2) A method for producing an atomized metal powder in which a fluid is jetted into a molten metal stream, the molten metal stream is divided to form a metal powder, and the metal powder is cooled.
- a method for producing an atomized metal powder wherein a metal flow is divided and the metal powder is cooled using spray water having a liquid temperature of 10 ° C. or less and a spray pressure of 5 MPa or more.
- the molten metal flow is made of an Fe—B alloy or an Fe—Si—B alloy, and the atomized metal powder is an amorphous metal powder.
- the present invention it is possible to rapidly cool a metal powder of 10 5 K / s or more by a simple method, and it is easy to obtain an atomized metal powder in an amorphous state.
- Metal powder can be manufactured easily and inexpensively, and it has a remarkable industrial effect.
- FIG. 1 is a graph showing the influence of cooling water temperature and injection pressure on the MHF point.
- FIG. 2 is an explanatory view schematically showing a schematic configuration of a water atomized metal powder production apparatus suitable for carrying out the present invention.
- FIG. 3 is an explanatory view schematically showing a schematic configuration of a gas atomized metal powder production apparatus suitable for carrying out the present invention.
- FIG. 4 is an explanatory view schematically showing an outline of a boiling curve.
- a metal material as a raw material is melted to form a molten metal.
- a metal material used as a raw material any of pure metals, alloys, pig irons and the like conventionally used as powders can be applied.
- iron-based alloys such as pure iron, low alloy steel, stainless steel, non-ferrous metals such as Ni and Cr, non-ferrous alloys, or amorphous alloys (amorphous alloys) such as Fe-B alloys, Fe-Si-B alloys Examples include alloys and Fe—Ni—B alloys. Needless to say, these alloys contain impurities in addition to the listed elements.
- the method for melting the metal material is not particularly limited, but any conventional melting means such as an electric furnace, a vacuum melting furnace, and a high-frequency melting furnace can be applied.
- the melted molten metal is transferred from a melting furnace to a container such as a tundish and is made into atomized metal powder in an atomized metal powder production apparatus.
- An example of a preferred water atomized metal powder production apparatus used in the present invention is shown in FIG.
- the molten metal 1 flows down from the container such as the tundish 3 as a molten metal flow 8 into the chamber 9 through the molten metal guide nozzle 4.
- an inert gas valve 11 is opened to create an atmosphere of inert gas (nitrogen gas, argon gas, etc.).
- the fluid 7 is sprayed on the molten metal flow 8 that has flowed down through the nozzle 6 disposed in the nozzle header 5, and the molten metal flow 8 is divided into a metal powder 8a.
- jet water water jet
- jet water (water jet) is used as the fluid 7.
- the jet water (water jet) to be used is jet water (water jet) having a liquid temperature of 10 ° C. or less and an injection pressure of 5 MPa or more.
- the liquid temperature (water temperature) of the jet water When the liquid temperature (water temperature) of the jet water is higher than 10 ° C., the water jet cooling at which the MHF point becomes a desired MHF point of about 1000 ° C. or higher cannot be achieved, and a desired cooling rate cannot be secured. For this reason, the liquid temperature (water temperature) of jet water was limited to 10 degrees C or less. In addition, Preferably it is 7 degrees C or less.
- the “desired cooling rate” here is the lowest cooling rate at which amorphization can be achieved, which is 10 on average from the temperature at which solidification is completed to the first crystallization temperature (for example, about 400 to 600 ° C.). The cooling rate is about 5 to 10 6 K / s.
- the injection pressure of the water jet (water jet) is less than 5 MPa, even if the water temperature of the cooling water is 10 ° C. or lower, it becomes impossible to perform water jet cooling in which the MHF point is higher than the desired temperature. Rapid cooling (desired cooling rate) cannot be ensured. For this reason, the jet pressure of jet water was limited to 5 MPa or more. Note that the injection pressure is preferably 10 MPa or less because the rise in MHF point is saturated even if the injection pressure exceeds 10 MPa.
- the molten metal flow is injected with the jet water adjusted in the water temperature and the injection pressure as described above, and the molten metal flow is divided and the divided metal powder (molten state) Cooling and solidifying at the same time.
- the cooling water used for the jet water is a heat exchanger such as a chiller 16 that cools the cooling water to a low temperature in advance in a cooling water tank 15 (heat insulating structure) provided outside the water atomized metal powder production apparatus 14. It is preferable to store it as low-temperature cooling water. Since a general cooling water production machine freezes the heat exchanger and it is difficult to generate cooling water of less than 3-4 ° C, a mechanism for replenishing ice into the tank is provided by the ice production machine. Also good. However, since the cooling water at 0 ° C. or less is likely to become ice, it is preferable that the cooling water exceeds 0 ° C. Furthermore, it goes without saying that the cooling water tank 15 is provided with a high-pressure pump 17 for boosting and feeding the cooling water and a pipe 18 for supplying the cooling water from the high-pressure pump to the nozzle header 5.
- a heat exchanger such as a chiller 16 that cools the cooling water to a low temperature in advance in a cooling water tank
- the molten metal flow may be divided by a gas atomizing method using an inert gas 22a.
- the divided metal powder is further cooled by spray water. That is, in the production of metal powder using the gas atomization method of the present invention, an inert gas is injected into the molten metal flow, the molten metal flow is divided, and the divided metal powder (including molten metal) is cooled.
- the injection pressure is 5 MPa or more and the water temperature is 10 ° C. or less.
- An example of a preferred gas atomized metal powder production apparatus used in the present invention is shown in FIG.
- the melted molten metal 1 is transferred from the melting furnace 2 to a container such as a tundish 3 and the molten metal flow 8 is transferred from the container into the chamber 9 through the molten metal guide nozzle 4 of the gas atomized metal powder production apparatus 19. As it flows down.
- bulb 11 is opened and the inside of the chamber 9 is made into inert gas atmosphere.
- An inert gas 22a is injected into the molten metal flow 8 that has flowed down through a gas injection nozzle 22 disposed in the gas nozzle header 21, and the molten metal flow 8 is divided into metal powder 8a. Then, the temperature of the obtained metal powder 8a is preferably about 1000 ° C., which is within the required cooling temperature range, to spray the water 25a to cool the metal powder 8a.
- the jet water 25a is jet water having a jet pressure of 5 MPa or more and a water temperature of 10 ° C. or less.
- cooling with injection water raises the MHF point to about 1000 ° C.
- cooling with spray water with a spray pressure of 5 MPa or more and a water temperature of 10 ° C. or less is preferably applied to metal powder having a temperature of approximately 1000 ° C. or less.
- the temperature of the metal powder can be adjusted by changing the distance from the gas atomization point to the start of jetting the jet water.
- the temperature of the metal powder 8a is higher than 1000 ° C. at the start of cooling with the jet water, even if the water temperature of the jet water is less than 5 ° C., cooling is caused by the film boiling state, and cooling starts at 1000 ° C. or less Compared to cooling in the transition boiling state, the cooling ability is lower, but the cooling ability is higher than the cooling in the normal film boiling state when the injection pressure is less than 5 MPa and the water temperature is 10 ° C. or more, and the film boiling state. Time can be shortened. Further, the MHF point can be increased by further lowering the water temperature and increasing the injection pressure, and the resulting metal powder has improved amorphousness. For example, by setting the water temperature to 5 ° C. or lower and the injection pressure to 10 MPa or higher, the MHF point can be raised to about 1030 ° C. This also makes the metal powder having a large particle size amorphous.
- the molten metal flow is divided by the gas atomization method, and then cooling is performed with the spray water having an injection pressure of 5 MPa or more and a water temperature of 10 ° C. or less.
- the temperature of the metal powder is equal to or lower than the MHF point, if the water jet cooling is performed under the above-described conditions, the cooling rate can be further increased.
- the cooling water used for the jet water is previously cooled to a low temperature in a cooling water tank 15 (heat insulating structure) provided outside the gas atomized metal powder production apparatus 19. It is preferable to store it as cooling water with a low water temperature in a heat exchanger such as the chiller 16. Further, a mechanism for supplying ice into the tank by an ice making machine may be provided. Needless to say, a gas cylinder 27 is disposed in the gas nozzle header 21 via a pipe 28. Furthermore, the cooling water tank 15 is provided with a high-pressure pump 17 for boosting and feeding the cooling water, and a pipe 18 for supplying the cooling water from the high-pressure pump to the cooling water injection nozzle 25. It goes without saying that the same applies.
- the critical cooling rate for amorphization varies depending on the alloy system. For example, in the case of an Fe—B alloy (Fe 83 B 17 ), 1.0 ⁇ 10 6 K / s, Fe—Si—B system is used. In the alloy (Fe 79 Si 10 B 11 ), 1.8 ⁇ 10 5 K / s is exemplified (Japan Society of Mechanical Engineers: Boiling heat transfer and cooling, P208, 1989, Nihon Kogyo Publishing). In addition, even in typical Fe-based and Ni-based amorphous alloys, the critical cooling rate for amorphization is about 10 5 to 10 6 K / s. As in the present invention, according to the metal powder manufacturing method that avoids the film boiling region from the beginning of cooling and performs cooling in the transition boiling region or the nucleate boiling region, it is possible to ensure the above-described cooling rate. is there.
- Example 1 Metal powder was manufactured using the water atomized metal powder manufacturing apparatus shown in FIG.
- the raw materials were blended so as to have a composition of 79% Fe-10% Si-11% B (Fe 79 Si 10 B 11 ) at at% (partially including impurities), and melting furnace 2 was melted at about 1550 ° C. to obtain about 50 kgf of molten metal.
- the melting furnace 2 After gradually cooling to 1350 ° C. in the melting furnace 2, it was poured into the tundish 3.
- the inside of the chamber 9 was previously opened with an inert gas valve 11 to create a nitrogen gas atmosphere.
- the high-pressure pump 17 is operated to supply cooling water from the cooling water tank 15 (capacity: 10 m 3 ) to the nozzle header 5 and from the water injection nozzle 6 to the injection water.
- (Fluid) 7 was left in a jetted state.
- the position where the molten metal flow 8 was in contact with the jet water (fluid) 7 was set at a position 200 mm from the molten metal guide nozzle 4.
- the molten metal 1 injected into the tundish 3 flows down into the chamber 9 through the molten metal guide nozzle 4 as a molten metal flow 8, and the jet water (fluid) whose water temperature and jet pressure are changed as shown in Table 1 ) was brought into contact with 7 and divided into metal powder, cooled while being mixed with cooling water, and recovered as metal powder from a recovery port provided with the metal powder recovery valve 13.
- the raw materials were blended so as to have a composition of 79% Fe-10% Si-11% B (Fe 79 Si 10 B 11 ) at at% (partially including impurities), and melting furnace 2 was melted at about 1550 ° C. to obtain about 10 kgf of molten metal.
- melting furnace 2 After gradually cooling to 1400 ° C. in a melting furnace, it was poured into the tundish 3. Note that the inside of the chamber 9 was previously opened with an inert gas valve 11 to create a nitrogen gas atmosphere.
- the high-pressure pump 17 is operated to supply cooling water from the cooling water tank 15 (capacity: 10 m 3 ) to the water injection nozzle 25 and to inject from the water injection nozzle 25. Water (fluid) 25a was jetted.
- the molten metal 1 injected into the tundish 3 flows down into the chamber 9 through the molten metal guide nozzle 4 as a molten metal flow 8, and argon gas (fluid) 22a injected from the gas nozzle 22 at an injection pressure of 5 MPa; It was made to contact and it divided and it was set as the metal powder 8a.
- the divided metal powder is cooled while solidifying by the action of heat radiation and atmospheric gas, and is cooled to about 1000 ° C., that is, 350 mm from the gas atomizing point (the contact point between the molten metal flow 8 and the argon gas 22a).
- the metal powder was cooled with spray water having the spray pressure and water temperature shown in Table 2, and recovered as metal powder from the recovery port provided with the metal powder recovery valve 13.
- the examples of the present invention had a crystallinity of less than 10% and were mostly amorphous metal powder.
- powder No. cooled using the spray water of the scope of the present invention powder No. cooled using the spray water of the scope of the present invention.
- the average temperature of the powder at the start of cooling was 1046 ° C., but the cooling pressure was increased by raising the MHF point to around 1050 ° C. by setting the injection pressure to 20 MPa and the water temperature to 4 ° C. It was confirmed that it was a metal powder.
- Example 3 Metal powder was manufactured using the gas atomized metal powder manufacturing apparatus shown in FIG.
- the raw materials were blended so that the composition of 83% Fe-17% B (Fe 83 B 17 ) was obtained at at% (partially including impurities), and melted at about 1550 ° C. in the melting furnace 2 As a result, about 10 kgf of molten metal was obtained.
- the mixture was poured into the tundish 3. Note that the inside of the chamber 9 was previously opened with an inert gas valve 11 to create a nitrogen gas atmosphere.
- the high-pressure pump 17 is operated to supply cooling water from the cooling water tank 15 (capacity: 10 m 3 ) to the water injection nozzle 25 and to inject from the water injection nozzle 25. Water (fluid) 25a was jetted.
- the molten metal 1 injected into the tundish 3 flows down into the chamber 9 through the molten metal guide nozzle 4 as a molten metal flow 8, and argon gas (fluid) 22a injected from the gas nozzle 22 at an injection pressure of 5 MPa; It was made to contact and it divided and it was set as the metal powder 8a.
- the divided metal powder is cooled while solidifying by the action of heat radiation and atmospheric gas, and when it is cooled to about 1000 ° C., that is, at a position 450 mm (partially 250 mm) from the gas atomization point, it appears on the metal powder. Cooling was carried out with the jet pressure and water temperature shown in Fig. 3, and the metal powder was recovered from the recovery port 13 as metal powder.
- the examples of the present invention had a crystallinity of less than 10% and were mostly amorphous metal powder.
- powder No. cooled using the spray water of the scope of the present invention In C4, the average temperature of the powder at the start of cooling is 1047 ° C., the injection pressure is 20 MPa, the water temperature is 4 ° C., and the MHF point is raised to around 1050 ° C. It was confirmed that
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Abstract
Description
(1)溶融金属流に、流体を噴射し、該溶融金属流を分断して金属粉末とし、該金属粉末を冷却するアトマイズ金属粉末の製造方法であって、前記流体を、液温:10℃以下、噴射圧:5MPa以上の噴射水として前記溶融金属流の分断および前記金属粉末の冷却を行うことを特徴とするアトマイズ金属粉末の製造方法。
(2)溶融金属流に、流体を噴射し、該溶融金属流を分断して金属粉末とし、該金属粉末を冷却するアトマイズ金属粉末の製造方法であって、前記流体を不活性ガスとして前記溶融金属流の分断を行い、前記金属粉末の冷却を、液温:10℃以下、噴射圧:5MPa以上の噴射水を用いて行うことを特徴とするアトマイズ金属粉末の製造方法。
(3)(2)において、前記噴射水の噴射を、前記金属粉末の温度が1000℃以下となった後に、行うことを特徴とするアトマイズ金属粉末の製造方法。
(4)(1)ないし(3)のいずれかにおいて、前記溶融金属流が、Fe-B系合金、あるいはFe-Si-B系合金からなり、前記アトマイズ金属粉末が非晶質金属粉末であることを特徴とするアトマイズ金属粉末の製造方法。
図2に示す水アトマイズ金属粉製造装置を用いて金属粉末を製造した。
(実施例2)
図3に示すガスアトマイズ金属粉製造装置を用いて金属粉末を製造した。
(実施例3)
図3に示すガスアトマイズ金属粉製造装置を用いて金属粉末を製造した。
2 溶解炉
3 タンディッシュ
4 溶湯ガイドノズル
5 ノズルヘッダー
6 ノズル(水噴射ノズル)
7 流体(噴射水)
8 溶融金属流
8a 金属粉末
9 チャンバー
10 ホッパー
11 不活性ガスバルブ
12 オーバーフローバルブ
13 金属粉回収バルブ
14 水アトマイズ金属粉製造装置
15 冷却水タンク
16 チラー(低温冷却水製造装置)
17 高圧ポンプ
18 冷却水配管
19 ガスアトマイズ金属粉製造装置
21 ノズルヘッダー(ガスノズルヘッダー)
22 ガスノズル
24 ヘッダーバルブ
25 冷却水噴射ノズル
25a 噴射水
26 冷却水用バルブ
27 ガスアトマイズ用ガスボンベ
28 高圧ガス配管
Claims (4)
- 溶融金属流に、流体を噴射し、該溶融金属流を分断して金属粉末とし、該金属粉末を冷却するアトマイズ金属粉末の製造方法であって、前記流体を、液温:10℃以下、噴射圧:5MPa以上の噴射水として、前記溶融金属流の分断および前記金属粉末の冷却を行うことを特徴とするアトマイズ金属粉末の製造方法。
- 溶融金属流に、流体を噴射し、該溶融金属流を分断して金属粉末とし、該金属粉末を冷却するアトマイズ金属粉末の製造方法であって、前記流体を不活性ガスとして前記溶融金属流の分断を行い、前記金属粉末の冷却を、液温:10℃以下、噴射圧:5MPa以上の噴射水を用いて行うことを特徴とするアトマイズ金属粉末の製造方法。
- 前記噴射水の噴射を、前記金属粉末の温度が1000℃以下となった後に、行うことを特徴とする請求項2に記載のアトマイズ金属粉末の製造方法。
- 前記溶融金属流が、Fe-B系合金、あるいはFe-Si-B系合金からなり、前記アトマイズ金属粉末が非晶質金属粉末であることを特徴とする請求項1ないし3のいずれかに記載のアトマイズ金属粉末の製造方法。
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CN201580016835.9A CN106132599B (zh) | 2014-03-31 | 2015-03-13 | 雾化金属粉末的制造方法 |
JP2015539900A JP6266636B2 (ja) | 2014-03-31 | 2015-03-13 | アトマイズ金属粉末の製造方法 |
SE1651221A SE542606C2 (en) | 2014-03-31 | 2015-03-13 | Method for producing atomized metal powder |
KR1020167027009A KR20160128380A (ko) | 2014-03-31 | 2015-03-13 | 아토마이즈 금속 분말의 제조 방법 |
KR1020187011451A KR102303461B1 (ko) | 2014-03-31 | 2015-03-13 | 아토마이즈 금속 분말의 제조 방법 |
US15/129,839 US10293407B2 (en) | 2014-03-31 | 2015-03-13 | Method of producing atomized metal powder |
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CN106132599A (zh) | 2016-11-16 |
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US20170144227A1 (en) | 2017-05-25 |
JPWO2015151420A1 (ja) | 2017-04-13 |
KR20180043853A (ko) | 2018-04-30 |
KR102303461B1 (ko) | 2021-09-16 |
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