WO2013150941A1 - 多孔質炭素材料の製造方法 - Google Patents
多孔質炭素材料の製造方法 Download PDFInfo
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- WO2013150941A1 WO2013150941A1 PCT/JP2013/059064 JP2013059064W WO2013150941A1 WO 2013150941 A1 WO2013150941 A1 WO 2013150941A1 JP 2013059064 W JP2013059064 W JP 2013059064W WO 2013150941 A1 WO2013150941 A1 WO 2013150941A1
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- porous carbon
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- carbide
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
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- C01B32/00—Carbon; Compounds thereof
- C01B32/05—Preparation or purification of carbon not covered by groups C01B32/15, C01B32/20, C01B32/25, C01B32/30
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- the present invention relates to a method for producing a porous carbon material.
- Patent Document 1 describes a method for producing porous activated carbon.
- Patent Document 2 describes a method for producing a graphite material that is porous and has a large specific surface area.
- Patent Documents 1 and 2 disclose that porous carbon is produced by reacting silicon carbide (SiC) with chlorine gas (Cl 2 ).
- Non-Patent Document 1 describes that a carbon material having nano-sized micropores can be generated by subjecting a metal carbide to a chlorination treatment.
- the metal carbide include SiC, TiC, B 4 C, and Al 4 C 3 . It is also shown that the porosity and pore size distribution of the carbon material differ depending on the type of metal carbide.
- a method for producing a porous carbon material there is a method of reacting a metal carbide such as SiC or TiC with chlorine gas. During this reaction, metal chlorides (SiCl 4 , TiCl 4, etc.) are also generated at the same time.
- conventional methods mainly employ a method of evaporating the metal chlorides and detoxifying them.
- a porous carbon material is produced industrially, a large amount of chlorine gas is consumed, so that such a method has a problem that the environmental load increases and the production cost also increases.
- This invention is made
- a method for producing a porous carbon material includes a metal carbide, which is a compound of a first metal and carbon, and chlorine gas, which are in contact with each other.
- a porous carbon generating step for generating a porous carbon material, and a first metal chloride and a second metal generated together with the porous carbon material in the porous carbon generating step are reacted with each other.
- Carbon production process, 1st The metal reduction step, the metal carbide generation step, and the second metal reduction step are repeatedly performed, and the metal carbide extracted by the metal carbide generation step is used for the porous carbon generation step, and is extracted by the second metal reduction step.
- Chlorine gas is used in the porous carbon production process, and the second metal taken out in the second metal reduction process is used in the first metal reduction process.
- metal carbide (SiC, TiC, etc.) reacts with chlorine gas (Cl 2 ) in the porous carbon generation step to generate porous carbon.
- the first metal chloride (SiCl 4 , TiCl 4, etc.) is generated at the same time.
- the first metal chloride is reduced by the first metal reduction step, and the first metal (Si, Ti, etc.) is taken out.
- the first metal thus taken out is carbonized in the metal carbide generating step, and metal carbide (SiC, TiC, etc.) is generated. This metal carbide is used again in the porous carbon production process described above.
- a second metal chloride (ZnCl 2 , MgCl 2, etc.) is also generated.
- This second metal chloride is reduced in the second metal reduction step, and second Are separated into metal (Zn, Mg, etc.) and chlorine gas (Cl 2 ).
- the second metal thus obtained is used again in the first metal reduction step described above.
- chlorine gas is used again in the porous carbon production
- the manufacturing method of the porous carbon material mentioned above all materials other than carbon used for the production
- the porous carbon material manufactured by this method can be widely used as an electrode such as a battery or an electric double layer capacitor, a catalyst carrier, activated carbon, and the like.
- the order of the metal carbide generation step and the second metal reduction step is not limited. That is, the metal carbide production step can be performed first, the second metal reduction step can be performed first, or these steps can be performed in parallel.
- the method for producing a porous carbon material may be characterized in that the metal carbide used in the porous carbon production step is powdery or porous.
- the metal carbide used in the porous carbon production step is powdery or porous.
- the manufacturing method of the porous carbon material is such that the metal carbide is Al 4 C 3 , B 4 C, CaC 2 , Cr 3 C 2 , Fe 3 C, SiC, ThC 2 , TiC, UC 2 , WC, and MoC. It is good also considering including at least one of these. Thereby, the porous carbon production
- the porous carbon generation step is performed by placing a metal carbide in a mixed gas atmosphere of chlorine gas and an inert gas, or in a chlorine gas atmosphere, and the mixed gas atmosphere or the chlorine gas atmosphere is set to 500 ° C. It can be performed by heating to a temperature of 1500 ° C. or lower.
- the method for producing a porous carbon material may be characterized in that the second metal is any one of a Group 1 element, a Group 2 element, a Group 11 element, and a Group 12 element.
- the 1st and 2nd metal reduction process mentioned above can be implemented suitably.
- the metal carbide is SiC
- the metal carbide is placed in a mixed gas atmosphere of chlorine gas and inert gas, or a chlorine gas atmosphere, and the mixed gas atmosphere or chlorine gas atmosphere is set to 900 ° C. or higher and 1300 ° C. It is possible to carry out by heating to a temperature of °C or less.
- SiC is used as a raw material
- it is advantageous that the raw material is relatively inexpensive and that the production of raw material SiC by the reaction between metal silicon, which is a reaction product after electrolysis, and carbon easily proceeds above the melting point of metal silicon. It becomes.
- the specific surface area takes the maximum value in the chlorination temperature range of 900 to 1300 ° C., and the characteristics as activated carbon are improved.
- the metal carbide is TiC
- the metal carbide is placed in a mixed gas atmosphere of chlorine gas and inert gas, or a chlorine gas atmosphere, and the mixed gas atmosphere or the chlorine gas atmosphere is set to 600 ° C. or higher and 1000 ° C. It is possible to carry out by heating to a temperature of °C or less.
- the reaction temperature is relatively low, and the production of raw material TiC by the reaction of titanium and carbon, which is a reaction product after electrolysis, easily proceeds above the melting point of the metal. It will be advantageous.
- the specific surface area takes the maximum value in the chlorination temperature range of 600 to 1000 ° C., and the value is larger than that of the SiC raw material, and the characteristics as the activated carbon are improved.
- the second metal can be any one of a Group 1 element, a Group 2 element, a Group 11 element, and a Group 12 element.
- the metals are desirable because they can be chlorinated by reaction with metal chlorides. Furthermore, it is more desirable that the metal itself has a high vapor pressure and a low melting point of chloride. Moreover, what does not form a solid solution with a metal component is more desirable.
- the metal carbide can be SiC and the second metal can be Zn.
- Zn is a desirable material because it is a combined reaction with SiCl 4 and does not form a solid solution with silicon, and has a relatively low melting point of chloride and a high vapor pressure of metal.
- the metal carbide can be TiC and the second metal can be Mg.
- Mg is desirable in combination with TiCl 4 because it does not form a solid solution with Ti, and the resulting chloride has a relatively low melting point and a high metal vapor pressure.
- the environmental load can be reduced and the production cost can be reduced.
- FIG. 1 is a figure showing each process of a manufacturing method of porous carbon material concerning an embodiment.
- FIG. 2 is a diagram schematically showing the configuration of the porous carbon generation apparatus 10 used in the porous carbon generation step.
- FIG. 3 is a diagram showing a simplified configuration of the zinc reduction device used in the first metal reduction step and the second metal reduction step.
- FIG. 4 is a diagram showing a specific configuration of the zinc reduction device.
- FIG. 5 is a diagram schematically showing a configuration of a metal carbide generating device used in the metal carbide generating step.
- FIG. 6 is a diagram illustrating each process of a modification of the embodiment. It is a table
- Drawing 1 is a figure showing each process of a manufacturing method of porous carbon material concerning an embodiment.
- the manufacturing method according to the present embodiment includes a porous carbon generation step S11, a first metal reduction step S12, a metal carbide generation step S13, and a second metal reduction step S14.
- a porous carbon generation step S11 a first metal reduction step S12, a metal carbide generation step S13, and a second metal reduction step S14.
- a porous carbon material is generated by performing a heat treatment by bringing a metal carbide, which is a compound of the first metal and carbon, and chlorine gas (Cl 2 ) into contact with each other.
- a metal carbide which is a compound of the first metal and carbon
- chlorine gas Cl 2
- X is an integer of 1 or more.
- the porous carbon forming step S11 is represented by the following formula (2). SiC + 2Cl 2 ⁇ SiCl 4 + C (2)
- a first metal M 1 and a chlorine gas Cl 2 reacts in a crystal composed of the first metal M 1 and carbon, thereby only the first metal M 1 comes out from the crystal, the porous A carbon structure is formed.
- a powdered metal carbide M in a mixed gas atmosphere of chlorine gas Cl 2 and an inert gas (N 2 , He, Ar, Ne, Xe, etc.) or a substantially 100% chlorine gas atmosphere. 1 C is placed, and the mixed gas atmosphere or the chlorine gas atmosphere is heated to a high temperature. At this time, the possible temperature of the mixed gas atmosphere or the chlorine gas atmosphere is, for example, 500 ° C. or more and 1500 ° C. or less.
- the metal carbide M 1 C is at least one of Al 4 C 3 , B 4 C, CaC 2 , Cr 3 C 2 , Fe 3 C, SiC, ThC 2 , TiC, UC 2 , WC, and MoC. Can be included.
- the first metal M 1 is at least one of Al, B, Ca, Cr, Fe, Si, Th, Ti, U, W, and Mo.
- the metal carbide M 1 C is preferably any of SiC, TiC, B 4 C, and WC.
- the melting point of the chloride produced by chlorination of these carbides is advantageous because it is relatively low temperature and can be easily condensed.
- the boiling point of WCl 5 is 300 ° C. or higher, it is a rare metal and works advantageously from the viewpoint of added value.
- the first metal chloride (M 1 Cl 2x in chemical formula (1) and SiCl 4 in chemical formula (2)) is obtained together with the porous carbon material.
- the first metal chloride M 1 Cl 2x is recovered by being cooled to around room temperature in a cooler or the like, for example.
- the metal M 1 of the first metal carbide M 1 C comes out efficiently, shortening the manufacturing time of the porous carbon material can do.
- the possible average particle diameter of the metal carbide M 1 C is 0.1 ⁇ m to 10 ⁇ m. Larger particle sizes are possible depending on the application, but if the particle size exceeds 500 ⁇ m, the diffusion reaction rate-limiting of the generated chloride becomes remarkable, which is not desirable.
- the first metal reduction step S12 is performed.
- the first metal chloride M 1 Cl 2X produced together with the porous carbon material in the porous carbon production step S11 is reacted with the second metal to react the first metal. It was allowed to reduction, take out the first metal M 1.
- the first metal reduction step S12 expressed by the following formula (3).
- Y is an integer of 1 or more.
- a first metal M 1 is, for example Si
- the second metal M 2 is, for example, Zn
- the first metal reduction step S12 expressed by the following formula (4).
- a high-purity first metal M 1 is extracted from the first metal chloride M 1 Cl 2X using a so-called zinc reduction method.
- the second metal M 2 can be chlorinated by the reaction with the first metal chloride M 1 Cl 2X to reduce the first metal M 1 , and the second metal reduction step S14 described later. Any element can be used as long as the chloride can be separated into chlorine gas and the second metal M 2 by electrolysis.
- a second metal M 2 are alkali metal (Group 1A element, also referred to as alkali metal), the Group 2 element (Group 2A element, also referred to as an alkaline earth metal), Group 11, such as Cu It can be either an element (also referred to as a Group 1B element) or a Group 12 element such as Zn (also referred to as a Group 2B element).
- the Group 1 element is any one of Li, Na, K, Rb, and Cs
- the Group 2 element is any one of Mg, Ca, Sr, Ba, and Ra.
- the group element is any one of Cu, Ag, and Au
- the group 12 element is any one of Zn, Cd, and Hg.
- Zn is a desirable material because it is a combination with SiCl 4 , does not form a solid solution with silicon, has a relatively low melting point of chloride, and has a high vapor pressure of metal.
- the metal can have a high vapor pressure, and Zn, Mg, Na, K, Sr and Ba are also possible.
- metal chlorides having a low melting point and not reacting with the substrate are possible.
- Zn, Mg, Na, K, Ca, and Sr are suitable (see the table in FIG. 8 (the table showing the melting point / boiling point of a metal and its metal chloride)).
- a metal carbide generation step S13 and a second metal reduction step S14 are performed. Note that either of these steps may be performed first or may be performed in parallel.
- the metal carbide M 1 C is generated by causing the first metal M 1 extracted in the first metal reducing step S12 to react with carbon.
- the carbon raw material used in the metal carbide generating step S13 can be easily available at a low cost, such as carbon black or natural graphite.
- generation process S13 is represented by following Chemical formula (5). M 1 + C ⁇ M 1 C (5) If the first metal M 1 is, for example, Si, the metal carbide forming step S13. Expressed by the following formula (6). Si + C ⁇ SiC (6) The metal carbide M 1 C taken out in the metal carbide generation step S13 is used again in the porous carbon generation step S11 described above.
- the second metal chloride (M 2 Cl 2X / Y in the chemical formula (3), chemical formula (3) is generated together with the first metal M 1 in the first metal reduction step S12.
- the second metal M 2 and the chlorine gas Cl 2 are taken out by reducing the second metal M 2 of ZnCl 2 ) in 4).
- This second metal reduction step S14 is represented by the following chemical formula (7).
- the second metal reduction step S14 expressed by the following formula (8).
- the second metal chloride M 2 Cl 2X / Y is electrolyzed in a high-temperature molten state, whereby the second metal chloride M 2 Cl 2X / Y is converted into the second metal M 2 and chlorine gas. It is separated into Cl 2. Then, the chlorine gas Cl 2 taken out in the second metal reduction step S14 is used again in the porous carbon generation step S11 described above. Further, the second metal M 2 taken out by the second metal reduction step S14, is used again in the first metal reduction second process S12 described above.
- FIG. 2 is a diagram schematically showing the configuration of the porous carbon generation apparatus 10 used in the porous carbon generation step S11.
- FIG. 3 is a diagram showing a simplified configuration of the zinc reduction device 20 used in the first metal reduction step S12 and the second metal reduction step S14.
- FIG. FIG. 5 is a diagram schematically showing the configuration of the metal carbide generating device 30 used in the metal carbide generating step S13.
- the porous carbon generator 10 includes a reaction furnace 11, a cooling trap 12, and a storage tank 13.
- the reaction furnace 11 accommodates a mounting shelf 11a on which the metal carbide M 1 C is placed over a plurality of stages, and the mounting shelf 11a is supported by being suspended from above by a support bar 11b.
- a gas introduction port 11c is provided in a portion of the reaction furnace 11 below the mounting shelf 11a. From this gas introduction port 11c, a mixed gas of chlorine gas Cl 2 and an inert gas, or substantially 100 is provided. % Chlorine gas Cl 2 is introduced into the reactor 11.
- a heater 11d is provided outside the reaction furnace 11 so as to surround the mounting shelf 11a.
- the mixed gas or chlorine gas around the metal carbide M 1 C is heated to a predetermined temperature of, for example, 500 ° C. or more and 1500 ° C. or less.
- a predetermined temperature for example, 500 ° C. or more and 1500 ° C. or less.
- the temperature range capable of this time depends on the type of metal carbide M 1 C, for example, when the metal carbide M 1 C is SiC, possible temperature range is 1600 ° C. or less 900 ° C. or higher.
- the reaction of the chemical formula (1) or (2) described above occurs, the first metal M 1 is released from the metal carbide M 1 C, and a porous carbon material is generated in the mounting shelf 11a.
- the first metal chloride M 1 Cl 2X (SiCl 4 is illustrated in the figure) and the mixed gas (or chlorine gas) generated by the reaction are supplied from the gas discharge port 11e provided in the upper part of the reaction furnace 11 to the reaction furnace. 11 is discharged to the outside.
- the gas discharge port 11 e is connected to the cooling trap 12, and the exhaust from the reaction furnace 11 is cooled by the refrigerant 12 a circulating in the cooling trap 12.
- the cooled first metal chloride M 1 Cl 2X is stored in the storage tank 13 and then sent to the zinc reduction device 20.
- the mixed gas (or chlorine gas) that has passed through the cooling trap 12 is exhausted to the outside of the porous carbon generator 10 through the three-way valve 14, or is sent again to the gas inlet 11c of the reactor 11. It is done.
- the zinc reduction device 20 includes vaporizers 21 and 22, a reaction furnace 23, and a molten salt electrolysis tank 24.
- the first metal chloride M 1 Cl 2X (SiCl 4 is illustrated in the figure) stored in the storage tank 13 of the porous carbon generator 10 described above is sent to the vaporizer 21 and vaporized.
- the second metal M 2 (Zn is illustrated in the figure) is vaporized.
- the first metal chloride M 1 Cl 2X and the second metal M 2 thus vaporized are sent to the reaction furnace 23.
- the vaporizer 22 includes an in-system charge vaporizer 22a, a continuous operation vaporizer 22b, and a collecting pipe 22c.
- the in-system charging carburetor 22a has a gate valve 22d, and can input the second metal M 2 (Zn is illustrated in the figure) from the outside of the zinc reduction device 20.
- the second metal M 2 is housed in the vaporization chamber 22e in-situ poured vaporizer 22a, it vaporizes.
- the vaporizing chamber 22e and the collecting pipe 22c are connected to each other by a pipe 22f.
- the vaporizer 22b for continuous operation includes a vaporization chamber 22g for accommodating the second metal M 2 taken out from the molten salt electrolyzer 24, vaporized.
- the vaporizing chamber 22g and the collecting pipe 22c are connected to each other by a pipe 22h.
- the piping 22h of the in-system charging carburetor 22a and the continuous operation carburetor 22b are made of, for example, ceramics (alumina or the like). Further, the vaporizing chamber 22g and the collecting pipe 22c of the continuous operation vaporizer 22b are made of, for example, carbon.
- the in-system charging carburetor 22a, the continuous operation carburetor 22b, and the collecting pipe 22c are heated to a high temperature of 900 ° C. to 1000 ° C.
- the reaction furnace 23 is, for example, a quartz container.
- the top of the reactor 23, through the quartz pipe 23a is coupled to the collecting pipe 22c of the vaporizer 22, the second metal M 2 is fed to the reactor 23 through a pipe 23a which is vaporized.
- the first metal chloride M 1 Cl 2X flows into the upper portion of the reaction furnace 23 via the quartz pipe 23b.
- the reaction furnace 23 is heated to a high temperature of 1200 ° C. to 1400 ° C., and the second metal M 2 and the first metal chloride M 1 Cl 2X react with each other inside the reaction furnace 23.
- the resulting first metal M 1 is accommodated in an unheated container 23 c provided inside the reaction furnace 23.
- the second metal chloride M 2 Cl 2X / Y passes through the fine particle trap 25 for removing the fine particles of the first metal M 1 and is then sent to the molten salt electrolytic cell 24.
- the fine particle trap 25 is made of, for example, quartz and is heated to a high temperature of 900 ° C. to 1000 ° C.
- the molten salt electrolytic cell 24 includes a main body 26 and an electrode structure 27.
- the main body portion 26 contains the molten second metal chloride M 2 Cl 2X / Y and electrolyzes an electrolyzer 26a and a heater (not shown) that is a heat source for heating the inside of the electrolyzer 26a. And have.
- a space 26b is provided above the electrolytic cell 26a, a pipe 26c connected to the particulate trap 25 is disposed at one end in the horizontal direction of the space 26b, and a pipe 26d (demister) is disposed at the other end.
- the second metal chloride M 2 Cl 2X / Y introduced from the pipe 26c is guided to the electrolytic cell 26a.
- Chlorine gas Cl 2 generated in the electrolytic bath 26a is discharged from the pipe 26d through the space 26b.
- a filter 28 made of Teflon resin is provided at the tip of the pipe 26d.
- the bottom of the electrolytic cell 26a is connected the pipe 26e is a second metal M 2 of high purity which is deposited on the bottom of the electrolytic cell 26a is fed through the pipe 26e to the continuous operation vaporizer 22b It is done.
- the electrode structure 27 has a plurality of electrode plates 27a.
- the plurality of electrode plates 27a are juxtaposed in the plate thickness direction with a gap, and are arranged in the electrolytic cell 26a with the plate thickness direction as a horizontal direction.
- the plurality of electrode plates 27a are made of a conductive material that is resistant to chlorine and resistant to chlorine, such as a high-purity carbon material, and are penetrated by one or more rod-shaped members 27b extending in the horizontal direction, so Relationship is maintained.
- a predetermined positive voltage is applied to the electrode plate 27a located at one end in the horizontal direction among the plurality of electrode plates 27a through an energization member 27c electrically connected to the electrode plate 27a. Functions as an anode.
- a predetermined negative voltage is applied to the electrode plate 27a located at the other end in the horizontal direction via an energizing member 27d electrically connected to the electrode plate 27a, and this electrode plate 27a functions as a cathode.
- the electrode plate 27a disposed between the anode and the cathode is given a potential gradient between the positive voltage and the negative voltage via an energizing member (not shown), and each of these electrode plates 27a serves as an intermediate electrode. Function.
- the second metal chloride M 2 Cl 2X / Y introduced from the pipe 26c is taken into the electrolytic cell 26a. Since the inside of the electrolytic cell 26a is maintained at a high temperature such as 500 ° C. to 700 ° C. by the heater, the second metal chloride M 2 Cl 2X / Y is maintained in a molten state. In addition, a plurality of electrode plates 27a are arranged inside the electrolytic cell 26a, and the plurality of electrode plates 27a are immersed in the molten second metal chloride M 2 Cl 2X / Y.
- each electrode plate 27a When a predetermined potential difference is applied to each electrode plate 27a, a current flows in the second metal chloride M 2 Cl 2X / Y through the opposing surfaces (electrolytic surfaces) of the adjacent electrode plates 27a, The second metal chloride M 2 Cl 2X / Y is electrolyzed to chlorine Cl 2 and the second metal M 2 .
- the second metal M 2 thus generated has a specific gravity greater than that of the melt of the second metal chloride M 2 Cl 2X / Y , and therefore accumulates at the bottom of the electrolytic cell 26a and is vaporized for continuous operation through the pipe 26e.
- the generated chlorine Cl 2 becomes chlorine gas, moves upward of the electrolytic cell 26a, and is sent to the porous carbon generator 10 through the pipe 26d.
- the metal carbide generating device 30 includes a reaction furnace 31 extending in the vertical direction, a heater 32 embedded in a side wall of the reaction furnace 31, and a mounting shelf 33 disposed in the reaction furnace 31. And.
- the mounting shelf 33, a mixture 34 of the first metal M 1 and a carbon material (e.g. carbon black or natural graphite) is placed across stages.
- the mounting shelf 33 is supported by being suspended from above by a support bar 33a.
- An intake port 31a is provided in the lower part of the reaction furnace 31, and an inert gas (N 2 , He, Ar, Ne, Xe, etc.) is introduced from the intake port 31a.
- the inert gas moves upward in the reaction furnace 31 and is then discharged from an exhaust port 31 b provided in the upper part of the reaction furnace 31.
- the heater 32 is disposed so as to surround the mounting shelf 33, and heats the mixture 34 mounted on the mounting shelf 33.
- the possible temperature of the mixture 34 in this step is 1400 ° C. to 1800 ° C.
- a reaction of the chemical formula (5) or (6) occurs, and the first metal M 1 and carbon are bonded to each other to generate a metal carbide M 1 C.
- the porous carbon generation step S11 metal carbide (for example, SiC) and chlorine gas (Cl 2 ) react to generate porous carbon.
- a first metal chloride for example, SiCl 4
- the first metal chloride is reduced by the first metal reduction step S12, and the first metal (for example, Si) is taken out.
- the first metal thus taken out is carbonized in the metal carbide generation step S13 to generate a metal carbide (for example, SiC).
- This metal carbide is used again in the porous carbon generation step S11 described above.
- a second metal chloride for example, ZnCl 2
- This second metal chloride is reduced in the second metal reduction step S14, and the second metal chloride is reduced. It is separated into metal (for example Zn) and chlorine gas (Cl 2 ).
- the second metal thus obtained is used again in the first metal reduction step S12 described above. Further, the chlorine gas is used again in the porous carbon generation step S11 described above.
- the method for producing a porous carbon material according to the present embodiment, all materials other than carbon used for the production of porous carbon can be circulated and reused. Therefore, according to this manufacturing method, the raw material efficiency can be increased, the environmental load can be reduced, and the production cost can be suppressed.
- the porous carbon material manufactured by this method can be widely used as an electrode such as a battery or an electric double layer capacitor, a catalyst carrier, activated carbon, and the like.
- FIG. 6 is a diagram illustrating each process of a modification of the embodiment. As shown in FIG. 6, the manufacturing method according to this modification example is similar to the above embodiment, in the porous carbon generation step S11, the first metal reduction step S12, the metal carbide generation step S13, and the second A metal reduction step S14, and a porous carbon material is produced by repeating these steps S11 to S14.
- TiC is used as the metal carbide in the porous carbon generation step S11. That is, this porous carbon production
- generation process S11 is represented by following Chemical formula (9). TiC + 2Cl 2 ⁇ TiCl 4 + C (9)
- TiCl 4 is obtained as the first metal chloride together with the porous carbon material. This TiCl 4 is recovered by being cooled to near room temperature in a cooler, for example.
- the first metal reduction step S12 is performed.
- Mg is used as the second metal. That is, this first metal reduction step S12 is represented by the following chemical formula (10). TiCl 4 + 2Mg ⁇ 2MgCl 2 + Ti (10) In this step, high-purity Ti is extracted from TiCl 4 .
- a metal carbide generation step S13 and a second metal reduction step S14 are performed. Note that either of these steps may be performed first or may be performed in parallel.
- TiC extracted in the first metal reduction step S12 reacts with each other to generate TiC.
- generation process S13 is represented by following Chemical formula (11). Ti + C ⁇ TiC (11) TiC taken out by this metal carbide generation step S13 is used again in the porous carbon generation step S11 described above.
- Mg and chlorine gas Cl 2 are taken out by reducing Mg of MgCl 2 generated together with Ti in the first metal reduction step S12.
- This second metal reduction step S14 is represented by the following chemical formula (12). MgCl 2 ⁇ Mg + Cl 2 (12)
- the chlorine gas Cl 2 taken out in the second metal reduction step S14 is used again in the porous carbon generation step S11 described above. Further, the Mg taken out in the second metal reduction step S14 is used again in the first metal reduction step S12 described above.
- Example 1 Examples in which a porous carbon material is actually manufactured according to the above embodiment will be described.
- activated carbon was used as the carbon raw material used in the metal carbide generating step S13.
- the activated carbon had an average particle size of 20 ⁇ m and a specific surface area of 80 m 2 / g.
- the mixture of the carbon raw material and metal silicon particles was placed on a carbon mounting shelf, and the mounting shelf was inserted into a reaction furnace set at 900 ° C. At this time, the atmospheric gas in the reaction furnace was nitrogen gas (N 2 ). After the insertion, the reaction was continued for 5 hours in a state where the metal silicon particles were melted by raising the temperature in the reaction furnace to 1450 ° C. at a temperature raising rate of 10 ° C./min.
- the product thus obtained was beta-type SiC.
- the SiC thus obtained was pulverized until the particle diameter became 10 ⁇ m, and then placed on a carbon mounting shelf of an electric furnace having a quartz glass furnace core tube. Then, the chlorine gas flow rate was set to 1000 ml / min, the Ar gas flow rate was set to 5000 ml / min, and processing was performed at a predetermined temperature for 1 hour. At this time, a cooling trap set at ⁇ 20 ° C. was provided at the exhaust port of the core tube, and SiCl 4 was liquefied by this cooling trap and dropped into the vessel. Further, Cl 2 that did not react with SiC in the core tube was refluxed to the core tube by a three-way valve installed on the outlet side of the cooling trap.
- the production of SiCl 4 was completed in about 50 minutes after the temperature was raised. Thereafter, the chlorine gas in the furnace core tube was removed by Ar gas, the carbon mounting shelf was pulled upward, the temperature was lowered to 400 ° C., and then taken out into the atmosphere.
- the treatment temperature is changed in increments of 100 ° C. in the range of 900 ° C. to 1500 ° C., and the adsorption isotherm of the obtained porous material is measured by the nitrogen adsorption method. From the obtained adsorption amount, the pore volume and the BET method are measured.
- Figure 11 is, X-ray diffraction waveform of the porous carbon material of the SiC raw material (Cu K alpha) are the indicated, each line shows the results of those different processing temperatures 11, the vertical axis represents the relative X-ray diffraction intensity, and the horizontal axis represents the diffraction angle 2 ⁇ (deg), where the waveform G1 is a measurement result at a processing temperature of 1000 ° C.
- G2 is a measurement result at a processing temperature of 1100 ° C.
- waveform G3 is a measurement result at a processing temperature of 1200 ° C.
- waveform G4 is a measurement result at a processing temperature of 1400 ° C.
- waveform G5 is a measurement result at a processing temperature of 1500 ° C.
- the generation process of the carbon material used in Fig. 11 is represented by the following chemical formula (13). SiC + 2Cl 2 ⁇ SiCl 4 + C (13)
- SiC raw material a broad peak in the region where the diffraction angle is 20 to 30 degrees and a peak near 43 degrees are confirmed.
- the sharp peaks at 22 ° and 26.2 ° are the crystal phase of the SiO 2 component (crystal or cristobalite) contained in the raw material.
- the (002) diffraction line of graphite is generated around 26 degrees, but the peak position of 20 to 30 degrees after removing small angle scattering of 10 degrees or less is 20 to 22 degrees, which is a plane spacing different from that of graphite crystals.
- the pore size and the like have changed greatly, there is no significant difference in the X-ray diffraction waveform in the range up to 1500 ° C.
- SiCl 4 liquefied by the cooling trap was heated to 80 ° C. and vaporized, and then this SiCl 4 and Zn vapor were reacted in a reaction vessel kept at 950 ° C.
- acicular metal silicon (Si) was generated in the reaction vessel.
- ZnCl 2 discharged from the reaction vessel was liquefied in a trap tank (550 ° C.), and then ZnCl 2 was decomposed by direct current electrolysis (electrode interval 10 mm, voltage 1.5 V). Chlorine gas generated by this decomposition was taken out through a filter and compressed (10 atm) in a chlorine gas storage tank to be liquefied. Further, molten Zn accumulated in the lower part of the electrolytic cell was sent to the vaporizer.
- the temperature was raised to 1450 ° C. in a vacuum and melted, and then the temperature was lowered and solidified.
- the purity was extremely high such as 99.9995%, and Zn and oxygen were confirmed as impurities.
- Example 2 Next, an example in which the porous carbon material is TiC will be described.
- activated carbon was used as the carbon raw material used in the metal carbide generating step S13.
- the activated carbon had an average particle size of 20 ⁇ m and a specific surface area of 800 m 2 / g.
- the mixture of the carbon raw material and metal titanium particles was placed on a carbon mounting shelf, and the mounting shelf was inserted into a reaction furnace set at 900 ° C. At this time, the atmospheric gas in the reaction furnace was nitrogen gas (N 2 ). After the insertion, the reaction was continued for 5 hours in a state where the metal silicon particles were melted by raising the temperature in the reaction furnace to 1550 ° C. at a temperature raising rate of 10 ° C./min. The product thus obtained was TiC.
- the TiC thus obtained was pulverized until the particle diameter became 10 ⁇ m and then placed on a carbon mounting shelf of an electric furnace having a quartz glass core tube. Then, the chlorine gas flow rate was set to 1000 ml / min, the Ar gas flow rate was set to 5000 ml / min, and processing was performed at a predetermined temperature for 1 hour. At this time, a cooling trap set at ⁇ 20 ° C. was provided at the exhaust port of the core tube, and TiCl 4 was liquefied by this cooling trap and dropped into the vessel. Further, Cl 2 that did not react with TiC in the core tube was refluxed to the core tube by a three-way valve installed on the outlet side of the cooling trap.
- TiCl 4 The production of TiCl 4 was completed in about 50 minutes after the temperature was raised. Thereafter, the chlorine gas in the furnace core tube was removed by Ar gas, the carbon mounting shelf was pulled upward, the temperature was lowered to 400 ° C., and then taken out into the atmosphere. The treatment temperature is changed in increments of 100 ° C. in the range of 800 ° C. to 1400 ° C., the adsorption isotherm of the obtained porous material is measured by the nitrogen adsorption method, and the pore volume and BET method are determined from the obtained adsorption amount.
- FIG. 10 shows the result of calculating the specific surface area according to the method and the average pore diameter according to the t method (change in surface physical properties due to the chlorination temperature (TiC raw material, treatment time 1 hour)).
- TiC raw material chlorination temperature
- Fig. 12 it was confirmed that a value of 1100 m 2 / g or more was obtained at 800 to 1100 ° C.
- An X-ray diffraction diagram of the crystal phase of the produced carbon material is shown in FIG. X-ray diffraction waveform of carbon material Cu K alpha) are the indicated, each line in with that.
- Figure 12 shows the results of those different processing temperatures, the vertical axis relative to display X-ray diffraction intensity and the horizontal axis and the diffraction angle 2 [Theta] (deg) 12
- a waveform G6 is a measurement result at a processing temperature of 1000 ° C.
- a waveform G7 is a measurement result at a processing temperature of 1100 ° C.
- a waveform G8 is a measurement result at a processing temperature of 1200 ° C.
- a waveform G9 is a processing temperature.
- a waveform G10 is a measurement result at a processing temperature of 1400 ° C.
- a broad peak in the region where the diffraction angle is 26 degrees and a peak near 43 degrees are confirmed.
- the (002) diffraction line of graphite is generated at around 26 degrees, it was confirmed that the specific surface area was reduced due to the growth of graphite crystals when the processing temperature was increased.
- the temperature was raised to 1750 ° C. in a vacuum to melt, and then the temperature was lowered and solidified.
- solidified titanium metal (Ti) was analyzed, the purity was extremely high such as 99.95%, and Mg and oxygen were confirmed as impurities.
- the method for producing a porous carbon material according to the present invention is not limited to the above-described embodiment, and various other modifications are possible.
- the metal carbide used in the porous carbon generation step and the second metal used in the first metal reduction step are not limited to those exemplified in the above embodiment.
- It can be used in a method for producing a porous carbon material that can reduce the environmental burden and reduce production costs.
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Abstract
Description
M1C+XCl2 → M1Cl2X+C ・・・(1)
第1の金属M1が例えばSiである場合、この多孔質炭素生成工程S11は次の化学式(2)で表される。
SiC+2Cl2 → SiCl4+C ・・・(2)
M1Cl2X+YM2 → YM2Cl2X/Y+M1 ・・・(3)
第1の金属M1が例えばSiであり、第2の金属M2が例えばZnである場合、この第1の金属還元工程S12は次の化学式(4)で表される。
SiCl4+2Zn → 2ZnCl2+Si ・・・(4)
M1+C → M1C ・・・(5)
第1の金属M1が例えばSiである場合、この金属炭化物生成工程S13は次の化学式(6)で表される。
Si+C → SiC ・・・(6)
この金属炭化物生成工程S13によって取り出された金属炭化物M1Cは、前述した多孔質炭素生成工程S11において再び用いられる。
M2Cl2X/Y → M2+(X/Y)Cl2 ・・・(7)
第2の金属M2が例えばZnである場合、この第2の金属還元工程S14は次の化学式(8)で表される。
ZnCl2 → Zn+Cl2 ・・・(8)
図6は、上記実施形態の一変形例の各工程を示す図である。図6に示されるように、本変形例による製造方法は、上記実施形態と同様に、多孔質炭素生成工程S11と、第1の金属還元工程S12と、金属炭化物生成工程S13と、第2の金属還元工程S14とを備えており、これらの工程S11~S14を繰り返し行うことによって多孔質炭素材料を生産する。
TiC+2Cl2 → TiCl4+C ・・・(9)
この工程では、多孔質炭素材料と共に、第1の金属塩化物としてTiCl4が得られる。このTiCl4は、例えば冷却器などにおいて室温付近まで冷却されることにより回収される。
TiCl4+2Mg → 2MgCl2+Ti ・・・(10)
この工程では、TiCl4から高純度のTiが取り出される。
Ti+C → TiC ・・・(11)
この金属炭化物生成工程S13によって取り出されたTiCは、前述した多孔質炭素生成工程S11において再び用いられる。
MgCl2 → Mg+Cl2 ・・・(12)
この第2の金属還元工程S14によって取り出された塩素ガスCl2は、前述した多孔質炭素生成工程S11において再び用いられる。更に、この第2の金属還元工程S14によって取り出されたMgは、前述した第1の金属還元工程S12において再び用いられる。
上記実施形態により多孔質炭素材料を実際に製造した実施例について説明する。この実施例では、金属炭化物生成工程S13に用いられる炭素原料として、活性炭を用いた。この活性炭の平均粒子径は20μmであり、比表面積は80m2/gであった。この炭素原料と金属シリコン粒子との混合物をカーボン製の載置棚に設置し、900℃に設定した反応炉の中にこの載置棚を挿入した。このとき、反応炉内の雰囲気ガスは、窒素ガス(N2)であった。挿入後、昇温速度10℃/分にて1450℃まで反応炉内を昇温することにより金属シリコン粒子を溶融させた状態で、5時間にわたり反応を継続した。こうして得られた生成物は、ベータ型のSiCであった。
SiC+2Cl2 → SiCl4+C ・・・(13)
SiC原料の場合、回折角度20~30度の領域のブロードなピークと、43度付近のピークとが確認される。22度、26.2度のシャープなピークは原料に含まれるSiO2成分(水晶ないしはクリストバライト)の結晶相である。グラファイトの(002)回折線は26度付近に生じるが、10度以下の小角散乱を除去した20~30度のピーク位置は20~22度となり、グラファイト結晶とは異なる面間隔となっている。細孔サイズなどは大きく変化しているが、1500℃までの範囲で、X線回折波形には大きな差は見られない。
多孔質炭素材料をTiCとした実施例について次に説明する。この実施例では、金属炭化物生成工程S13に用いられる炭素原料として、活性炭を用いた。この活性炭の平均粒子径は20μmであり、比表面積は800m2/gであった。この炭素原料と金属チタン粒子との混合物をカーボン製の載置棚に設置し、900℃に設定した反応炉の中にこの載置棚を挿入した。このとき、反応炉内の雰囲気ガスは、窒素ガス(N2)であった。挿入後、昇温速度10℃/分にて1550℃まで反応炉内を昇温することにより金属シリコン粒子を溶融させた状態で、5時間にわたり反応を継続した。こうして得られた生成物は、TiCであった。
TiC+2Cl2 → TiCl4+C ・・・(14)
TiC原料の場合、回折角度26度の領域のブロードなピークと、43度付近のピークとが確認される。グラファイトの(002)回折線は26度付近に生じるが、処理温度を高めるとグラファイト結晶が成長していくことにより、比表面積の減少が生じていることを確認できた。
Claims (10)
- 第1の金属と炭素との化合物である金属炭化物と塩素ガスとを互いに接触させて加熱処理を行い、多孔質炭素材料を生成する多孔質炭素生成工程と、
前記多孔質炭素生成工程において前記多孔質炭素材料と共に生成される第1の金属塩化物と第2の金属とを反応させ、前記第1の金属を取り出す第1の金属還元工程と、
前記第1の金属還元工程において取り出された前記第1の金属と炭素とを相互に反応させて前記金属炭化物を生成する金属炭化物生成工程と
を備え、
前記第1の金属還元工程において前記第1の金属と共に生成される第2の金属塩化物を還元させて前記第2の金属および塩素ガスを取り出す第2の金属還元工程を前記第1の金属還元工程の後に更に備えることを特徴とする、多孔質炭素材料の製造方法。 - 前記多孔質炭素生成工程、前記第1の金属還元工程、前記金属炭化物生成工程、及び前記第2の金属還元工程を繰り返し行うとともに、前記金属炭化物生成工程によって取り出された前記金属炭化物を前記多孔質炭素生成工程に用い、前記第2の金属還元工程によって取り出された前記塩素ガスを前記多孔質炭素生成工程に用い、前記第2の金属還元工程によって取り出された前記第2の金属を前記第1の金属還元工程に用いる
ことを特徴とする、請求項1に記載の多孔質炭素材料の製造方法。 - 前記多孔質炭素生成工程において用いられる前記金属炭化物が粉末状ないしは、多孔質体であることを特徴とする、請求項1に記載の多孔質炭素材料の製造方法。
- 前記金属炭化物が、Al4C3、B4C、CaC2、Cr3C2、Fe3C、SiC、ThC2、TiC、UC2、WC、及びMoCのうち少なくとも一つを含むことを特徴とする、請求項1~3のいずれか一項に記載の多孔質炭素材料の製造方法。
- 前記多孔質炭素生成工程を、前記塩素ガスと不活性ガスとの混合ガス雰囲気、若しくは前記塩素ガス雰囲気に前記金属炭化物を置き、前記混合ガス雰囲気若しくは前記塩素ガス雰囲気を500℃以上1500℃以下の温度に加熱して行うことを特徴とする、請求項1~4のいずれか一項に記載の多孔質炭素材料の製造方法。
- 前記多孔質炭素生成工程において、金属炭化物がSiCであり、前記塩素ガスと不活性ガスとの混合ガス雰囲気、若しくは前記塩素ガス雰囲気に前記金属炭化物を置き、前記混合ガス雰囲気若しくは前記塩素ガス雰囲気を900℃以上1300℃以下の温度に加熱して行うことを特徴とする、請求項1~3のいずれか一項に記載の多孔質炭素材料の製造方法。
- 前記多孔質炭素生成工程において、金属炭化物がTiCであり、前記塩素ガスと不活性ガスとの混合ガス雰囲気、若しくは前記塩素ガス雰囲気に前記金属炭化物を置き、前記混合ガス雰囲気若しくは前記塩素ガス雰囲気を600℃以上1000℃以下の温度に加熱して行うことを特徴とする、請求項1~3のいずれか一項に記載の多孔質炭素材料の製造方法。
- 前記第2の金属が、第1族元素、第2族元素、第11族元素、及び第12族元素のうち何れかであることを特徴とする、請求項1~7のいずれか一項に記載の多孔質炭素材料の製造方法。
- 前記多孔質炭素生成工程において、金属炭化物がSiCであり、前記第2の金属がZnであることを特徴とする、請求項1~6のいずれか一項に記載の多孔質炭素材料の製造方法。
- 前記多孔質炭素生成工程において、金属炭化物がTiCであり、前記第2の金属が、Mgであることを特徴とする、請求項1~5、7のいずれか一項に記載の多孔質炭素材料の製造方法。
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