1. Field of the Invention
The present invention relates to a method for manufacturing a metallic material having a composite metal structure consisting of a non-ferrous metal alloy such as magnesium alloy or aluminum alloy and a carbon nanomaterial.
2. Description of the Related Art
The carbon nanomaterial that is one kind of crystalline carbon materials has characteristics such as having about 5 times higher heat conductivity than non-ferrous metals such as aluminum (Al) and magnesium (Mg), satisfactory electric conductivity, and excellent slidability due to low friction factor. However, the carbon nanomaterial is recommendable to be made into a composite by mixing with other substances in application thereof because it is an ultrafine material of nm scale.
A conventionally known art for compositing a metallic material with a carbon nanomaterial comprises kneading the carbon nanomaterial with a metal powder followed by pressure refining to form composite material grains having a metal powder grain size of 5 μm to 1 nm, and the composite material grains are thermally compressed by hot press molding, and processed into a product consisting of a composite metallic material. However, since the product shape is restricted in this product processing by hot press molding, this method stops short of manufacturing a metal product such as a heat radiating part or shield part for electronic equipment or a bearing which was difficult to manufacture by press molding.
Therefore, it has been tried to form a composite metallic material adaptable for a metal molding machine by perfectly melting a metallic material to a temperature of a liquidus temperature or higher, adding carbon nanomaterial to the metallic material of in the liquid phase state, and stirring and kneading the metallic material with the carbon nanomaterial by a stirring machine. However, since the carbon nanomaterial is poor in wettability with the metallic material in the liquid phase state and is difficult to be dispersed uniformly in the liquid phase due to floating by stirring, this method has not been put into practical use, so far.
As a new means for uniformly dispersing the carbon nanomaterial, it has been performed to cool a molten metallic material from a liquid state into a semi-solid state, spheroidize granular solid phase in a liquid phase which is generated in this cooling process to form a semi-solid metallic material showing thixotropic properties, and add the carbon nanomaterial thereto followed by stirring and kneading. Although this spheroidization of solid phase is performed by flowing down the metallic material over the plate surface of an inclined cooling plate in a molten state thereof, the spheroidization can be performed also by adding a crystal grain refining agent or by assigning an electromagnetic vibration force or an ultrasonic vibration force.
Although the dispersion of the carbon nanomaterial is enhanced in the above-mentioned compositing with the metallic material in the semi-solid state, compared to the compositing with the metallic material molten to the liquid phase state, part of the carbon nanomaterial is left in lumps in the liquid phase between solid phases as it is coagulated. This is caused by the fact that the carbon nanomaterial itself is easy to coagulate, and the dispersion is limited to the liquid phase between solid phases, and the coagulation cannot be entirely broken and dispersed by the stirring by rotation of a stirring blade, and homogenization of the composite metal structure had its limit. When ultrasonic vibration is adapted as a stirring means by vibration, the carbon nanomaterial floats on the surface layer of the semi-solid metallic material by the vibration, and mostly left in the upper layer, and the resulting difference in density of the carbon nanomaterial between the upper layer and the lower layer makes it difficult to bring the composite metal structure into a homogenous state.
The present invention has been achieved to solve the above-mentioned problems. An object of the present invention is to provide a method for manufacturing a composite of a carbon nanomaterial and a metallic material suitable as a molding material for injection molding, die-cast molding or the like, which has a homogeneous composite metal structure and shows thixotropic properties in a semi-solid state by performing compositing of a metallic material with a carbon nanomaterial by using both stirring and vibration.
According to the present invention, in compositing of a metallic material of a non-ferrous metal alloy with a carbon nanomaterial by adding the carbon nanomaterial in a state where the metallic material shows thixotropic properties by spheroidization of solid phase in a semi-solid state thereof, the compositing is performed by a process for stirring and kneading the metal material of the semi-solid state while keeping the temperature thereof at a solid-liquid coexisting temperature and by a process for dispersing the carbon nanomaterial to the liquid phase between solid phases by ultrasonic vibration.
The spheroidization of solid phase in the semi-solid state of the metallic material is performed in the process of cooling the metallic material into the semi-solid state by flowing down the metallic material, after melting it by heating to a liquidus temperature or higher, over the plate surface of an inclined cooling plate. Otherwise, the spheroidization of solid phase is performed by melting the metallic material to the semi-solid state by heating to a solid-liquid coexisting temperature between a liquidus temperature or lower and a solidus temperature or higher, and shearing the solid phase by stirring the semi-solid metallic material.
The stirring and kneading process is performed by adding the carbon nanomaterial in the spheroidization process of shearing the solid phase by stirring the semi-solid metallic material.
The dispersion process by ultrasonic vibration comprises continuously or intermittently assigning ultrasonic vibration for 60 to 900 seconds successively to the stirring and kneading process, and the ultrasonic vibration is assigned with a frequency of 5 to 30 kHz, an ultrasonic wave output of 500 to 3000 kW, an amplitude width of 5 to 30 μm, and a vibration giving time of 60 to 900 seconds.
The non-ferrous metal alloy is a magnesium alloy, grains of solid phase of the semi-solid metallic material has a size of 50 to 300 μm, and the grains are refined to 5 to 50 μm by the ultrasonic vibration.
The carbon nanomaterial consists of a carbon nanofiber having a diameter of 10 to 150 nm and a length of 1 to 100 μm, and the addition amount of the carbon nanomaterial is 0.1 to 20 mass %. The carbon nanomaterial is preheated before added to the semi-solid metallic material.
In the above-mentioned structure, since the stirring and kneading of the metallic material with the carbon nanomaterial is performed in a semi-solid state where liquid phase and solid phase are coexistent, even the carbon nanomaterial, which is poor in wettability with the metallic material in the liquid phase state and is difficult to knead due to floating to the molten metal surface by stirring, can be easily mixed with the metallic material since the floating of the carbon nanomaterial is suppressed by limitation of its dispersion range to the liquid phase between solid phases due to the presence of spheroidized solid phase, viscosity increased by the carbon nanomaterial dispersed to the liquid phase, or the like.
Further, since the lumps caused by coagulation of the carbon nanomaterial are broken and dispersed to the liquid phase by the stirring and the assignment of ultrasonic vibration, and the carbon nanomaterial is entirely dispersed by extension of the dispersion range by refining of solid phase by ultrasonic vibration, a homogeneous and thixotropic composite of carbon nanomaterial and metallic material for molding, which was difficult to manufacture by conventional compositing only by stirring or ultrasonic vibration can be easily manufactured.
The non-ferrous metal alloy in the present invention means an alloy based on any one of magnesium (Mg), tin (Sn), aluminum (Al), copper (Cu), lead (Pb), and zinc (Zn).
The manufacturing process of a composite metallic material of an alloy based on magnesium (AZ91D: liquidus temperature 595° C.) with a carbon nanomaterial will be described according to the above-mentioned process flow. The carbon nanomaterial is a carbon nanotube and a carbon nanofiber having a diameter of 10 to 150 nm and a length of 1 to 100 μm.
The melting furnace 1 is first heated to 595 to 750° C. to perfectly melt the metallic material put into the melting furnace at a liquidus temperature or higher. A fixed amount of a resulting molten metallic material M1 is poured onto the upper end of the inclined cooling plate 2 through the supply and discharge pipe 13 of the melting furnace 1, and flowed down over the plate surface to the storage container 3 maintained at a semi-solid temperature at the lower end.
The molten metallic material M1 is cooled to a liquidus temperature or lower in the process of flowing down over the inclined cooling plate 2. During the course, primary crystal seeds by solidification and spheroidization of a component having a high melting point of the alloy components are formed, and the molten material M1 is consequently stored as a semi-solid metallic material M2 showing thixotropic properties in which solid phase and liquid phase are coexistent in the storage container 3 maintained at the solid-liquid coexisting temperature. The grain size of solid phase in the storage container 3 is 50 to 200 μm (stored within 5 minutes).
The storage container 3 is then moved to the position of the stirring device 4, and the stirring bar 41 with blades is inserted into the storage container from above, and a predetermined amount (e.g., 1 mass %) of carbon nanomaterial C is added while stirring the semi-solid metallic material M2 maintained at the solid-liquid coexisting temperature by the electric furnace 31. The stirring is performed for at least 10 minutes or more (rotating speed: 500-3000 rpm), including the addition time thereof. If the solid phase ratio of solids in the stirring and kneading is 10% or less, dispersion of the carbon nanomaterial is apt to be uneven because the liquid phase area in which the carbon nanomaterial is dispersed is too large and the solid phase for suppressing the floating of the carbon nanomaterial is too small. If the solid phase ratio exceeds 90%, the liquid phase area is narrowed to make the dispersion difficult.
The carbon nanomaterial C is preferably preheated (e.g., to 500° C.) prior to its addition. This preheating can arrest reduction in temperature of the semi-solid metallic material M2 after the addition. The carbon nanomaterial C at the time of addition is in a coagulated state and difficult to break as it is, but dispersed, in the semi-solid metallic material, to the liquid phase between solid phases by the kneading and stirring. However, it is partially dispersed as small lumps as it is coagulated. Such lumps are never broken even if the rotating speed of the stirring bar 41 is raised or the stirring time is prolonged, and left in such a manner that they are sandwiched between solid phases.
When the stirring of the carbon nanomaterial C is ended, the stirring device 4 is replaced by the ultrasonic vibration generator 5, the vibration hone 51 is inserted into a semi-solid metallic material M3 primarily composited with the carbon nanomaterial C by stirring, and ultrasonic vibration (amplitude direction: vertical) is assigned to the semi-solid metallic material M3. The solid phase is refined by this vibration assignment to increase the area of liquid phase between solid phases, and the lumps coagulated between solid phases are also broken and dispersed by the ultrasonic vibration. Consequently, the carbon nanomaterial C is uniformly dispersed.
The ultrasonic vibration assigned to the semi-solid metallic material M3 can be assigned with a frequency of 5 to 30 kHz, an ultrasonic output of 500 to 3000 kW, an amplitude of 5 to 30 μm, and an assignment time of 60-900 seconds, and the assignment of ultrasonic vibration can be performed continuously or intermittently. Depending on the breaking state of the coagulation, repetitive intermittent assignment of ultrasonic vibration may be preferred. In the semi-solid metallic material M3 to which the ultrasonic vibration is assigned, grains of solid phase are refined to 5 to 50 μm.
After the lapse of a set time, the semi-solid metallic material M3 composited with the carbon nanomaterial C is poured into the mold 6 and cast into a metallic material M4 for molding process of a short columnar shape (bar), an ingot or the like.
In the above-mentioned embodiment, after the metallic material is melted by heating to a liquidus temperature or higher, the metallic material is flowed down over the inclined cooling plate, whereby generation and spheroidization of solid phase in the semi-solid metallic material are performed. Besides, the spheroidization can be performed by holding the semisolid metallic material by heating to a solid-liquid coexisting temperature between a liquidus temperature or lower and a solidus temperature or higher, and granularly shearing the resulting solid phase by stirring. In this case, after the metallic material is molten into the partially molten state by heating the storage container 3 shown in
In this spheroidization of granular solid phase by stirring shearing, although the grain size of solid phase is as large as 100 to 300 μm (melting temperature: 585° C., stirring time: 30 minutes, rotating speed: 500 rpm), compared with the spheroidization by flowing down over the inclined cooling plate, it never makes the subsequent stirring and kneading difficult since the average grain size is about 100 μm.
In the above-mentioned embodiment, although the ultrasonic vibration is assigned after the stirring and kneading process of the carbon nanomaterial, the assignment of ultrasonic vibration can be performed simultaneously with the stirring. In this case, since the compositing treatment by ultrasonic vibration can be performed within the stirring time, the manufacturing time can be shortened.
Number | Date | Country | Kind |
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2006-134175 | May 2006 | JP | national |