Method for producing intermetallic compound powder, method for producing intermetallic compound sintered body, intermetallic compound sintered body, and thermoelectric conversion element

Abstract

To obtain fine and homogeneous intermetallic compound powder in pulverization by a medium stirring type pulverizer.SOLUTION: A method for producing intermetallic compound powder includes a step of adding nanoceramic powder to metal raw material powder containing a plurality of metal elements to pulverize it using a medium stirring type pulverizer.SELECTED DRAWING: Figure 1

Description

[Technical Field]

[0001] The present invention relates to a method for producing intermetallic compound powder, a method for producing an intermetallic compound sintered body, and technologies for intermetallic compound powder, intermetallic compound sintered body, and thermoelectric conversion elements. [Background technology]

[0002] From the perspective of efficiently utilizing energy, various energy conversion technologies have been proposed that convert waste heat into electricity. For example, there are thermoelectric materials that can directly convert thermal energy into electrical energy by utilizing the Seebeck effect. It is widely known that intermetallic compounds with thermoelectric properties are used as thermoelectric materials. Furthermore, in order to improve the performance of thermoelectric conversion elements by suppressing thermal conductivity, miniaturization and homogenization of thermoelectric materials are necessary.

[0003] To miniaturize thermoelectric materials, a media-agitated pulverizer (e.g., a ball mill or attritor) using a pulverizing medium such as balls is used in the production of intermetallic compound powders (e.g., Patent Document 1). Specifically, by introducing metal raw material powder into a media-agitated pulverizer and causing it to collide with the pulverizing medium, the metal raw material powder is repeatedly compressed and pulverized to produce fine intermetallic compound powder. For example, Bi2Te3, a typical thermoelectric material, is highly brittle and can be easily miniaturized using a media-agitated pulverizer. [Prior art documents] [Patent Documents]

[0004] [Patent Document 1] Japanese Patent Application Publication No. 5-148513 [Overview of the project] [Problems that the invention aims to solve]

[0005] However, when producing intermetallic compound powders using a media-stirring pulverizer, agglomeration accompanied by adhesion to the pulverizing container and pulverizing medium can prevent sufficient pulverization and mixing of the metal raw material powder. Consequently, the intermetallic compound powder is not only not finely ground but also heterogeneous. In particular, with half-Heusler alloys such as TiNiSn, which have high thermoelectric performance in the medium temperature range and are expected to be used as thermoelectric materials for waste heat recovery, the metal raw material powder has high ductility, and the agglomeration problem is particularly pronounced.

[0006] Furthermore, when homogenizing half-Heusler alloys such as TiNiSn, there is a method that stabilizes thermoelectric performance by homogenizing the composition through long-term heat treatment lasting from tens of hours to several days. However, such long-term heat treatment consumes a tremendous amount of energy, making it undesirable from a practical standpoint.

[0007] In consideration of the above circumstances, the present invention aims to provide a manufacturing method for producing fine and homogeneous intermetallic compound powder by grinding with a media-stirring type pulverizer, intermetallic compound powder, a sintered body obtained by sintering the intermetallic compound powder, and a thermoelectric conversion element made from the sintered body. [Means for solving the problem]

[0008] [1] The method for producing intermetallic compound powder according to the present invention includes the step of adding nanoceramics powder to a metal raw material powder containing multiple metal elements and grinding it using a medium-stirring type pulverizer.

[0009] [2] A method for producing the intermetallic compound powder according to [1], wherein the average particle size of the nanoceramic powder is 100 nm or less.

[0010] [3] A method for producing intermetallic compound powder according to [1] or [2], wherein the nanoceramics powder is added in an amount of 0.5 vol% or more and 5.0 vol% or less relative to the total amount of the metal raw material powder and the nanoceramics powder.

[0011] [4] The method for manufacturing the intermetallic compound powder according to any one of [1] to [3] above, wherein the nanoceramics powder is an oxide-based ceramic.

[0012] [5] The method for manufacturing the intermetallic compound powder according to [4] above, wherein the oxide-based ceramic is one or more selected from Al2O3, MgO, La2O3, and ZrO2.

[0013] [6] The method for manufacturing the intermetallic compound powder according to any one of [1] to [5] above, wherein the metal raw material powder is a powder after subjecting the plurality of metal elements to a solid-phase reaction.

[0014] [7] The method for manufacturing an intermetallic compound sintered body according to the present invention includes a step of sintering a composite powder material in which nanoceramics are dispersed in an intermetallic compound.

[0015] [8] The method for manufacturing an intermetallic compound sintered body according to [7] above, wherein the content of the nanoceramics is 0.5 vol% or more and 5.0 vol% or less with respect to the total of the intermetallic compound and the nanoceramics.

[0016] [9] The method for manufacturing an intermetallic compound sintered body according to [7] or [8] above, wherein in the step, the composite powder material is sintered by electric current-assisted pressure sintering.

[0017]

[10] The intermetallic compound powder according to the present invention is a composite powder material in which nanoceramics are dispersed in an intermetallic compound.

[0018]

[11] The intermetallic compound powder according to

[10] above, wherein the content of the nanoceramics is 0.5 vol% or more and 5.0 vol% or less with respect to the total of the intermetallic compound and the nanoceramics.

[0019]

[12] The intermetallic compound powder according to

[10] or

[11] above, which is used as a thermoelectric material.

[0020]

[13] The intermetallic compound sintered body according to the present invention is a sintered body of any one of the intermetallic compound powders from the above

[10] to the above

[12] .

[0021]

[14] The intermetallic compound sintered body according to the above

[13] , wherein the content of the nanoceramics is 0.5 vol% or more and 5.0 vol% or less with respect to the total of the intermetallic compound and the nanoceramics.

[0022]

[15] The intermetallic compound sintered body according to the above

[13] or the above

[14] , wherein the weight change at 600 °C based on 0 °C in thermogravimetric measurement is 100 to 100.2%.

[0023]

[16] The thermoelectric conversion element according to the present invention is made of any one of the intermetallic compound sintered bodies from the above

[13] to the above

[15] .

Advantages of the Invention

[0024] According to the method for producing an intermetallic compound powder of the present invention, it is possible to suppress the aggregation of the metal raw material powder in a medium stirring type grinder. Therefore, fine and homogeneous intermetallic compound powder can be obtained. Further, the intermetallic compound sintered body produced from the intermetallic compound powder produced by the method for producing an intermetallic compound powder of the present invention has an advantage of excellent heat resistance.

Brief Description of the Drawings

[0025] [Figure 1] It is a figure which shows the SEM image of the sintered body which concerns on Example 1-1 and Comparative Example 1. [Figure 2] It is a figure which shows the result of the X-ray diffraction measurement of the sintered body which concerns on Example 1-1 and Comparative Example 1. [Figure 3] It is a figure which shows the thermoelectric characteristics of the sintered body which concerns on Example 1-1 and Comparative Example 1. [Figure 4] It is a figure which shows the thermoelectric characteristics of the sintered body which concerns on Example 1-2 and Comparative Example 1. [Figure 5] It is a figure which shows the thermoelectric characteristics of the sintered body which concerns on Example 1-3, 1-4 and Comparative Example 1. [Figure 6] This figure shows the results of thermogravimetric analysis of the sintered bodies according to Example 1-1 and Comparative Example 1. [Figure 7] This figure shows the results of thermogravimetric analysis of the sintered bodies according to Examples 1-2 and Comparative Example 1. [Modes for carrying out the invention]

[0026] <Intermetallic compound powder> The intermetallic compound powder according to the present invention has thermoelectric properties and is suitably used as a thermoelectric material capable of converting thermal energy into electrical energy. The intermetallic compound powder of the present invention is fine and homogeneous. Furthermore, the intermetallic compound powder of the present invention is used to obtain an intermetallic compound sintered body. The obtained intermetallic compound sintered body (hereinafter simply referred to as "sintered body") has the advantage of being fine and homogeneous, and also having high heat resistance.

[0027] Specifically, intermetallic compound powder is a composite powder material in which nanoceramics are dispersed in an intermetallic compound. For example, intermetallic compound powder is a composite formed by the combination of an intermetallic compound and nanoceramics. Furthermore, intermetallic compound powder may also be a solid solution in which the nanoceramics are solidly dissolved in the intermetallic compound. However, it is not essential that the entire intermetallic compound powder be composite or in a solid solution.

[0028] The average particle size of intermetallic compound powder is not particularly limited, but is, for example, 0.5 to 100 μm. The average particle size of intermetallic compound powder refers to the particle size at 50% of the integrated value of the particle size distribution determined by laser diffraction-scattering (d50).

[0029] The primary particle size (average primary particle size) of intermetallic compound powder is not particularly limited, but is for example, 10 nm to 5 μm. The primary particle size of intermetallic compound powder can be determined, for example, by SEM observation or X-ray diffraction measurement. In SEM observation, the particle size (maximum diameter) can be measured for any number of primary particles (100 particles), and the primary particle size can be determined as the average value of these measurements.

[0030] In intermetallic compound powders, the intermetallic compound is a compound composed of two or more metal elements.

[0031] The metal elements in intermetallic compounds include not only the metal elements of groups 1 to 15 of the periodic table, but also metalloid elements (B, Si, Ge, As, Sb, Te). For example, one or more of the following metal elements can be selected: Al, Si, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, Ge, Se, Y, Zr, Nb, Mo, Ru, Rh, Tl, Pd, Ag, Cd, In, Sn, Sb, La, Ce, Hf, Ta, W, Re, Os, Ir, Pt, Au, Pb, Te, and Bi. Among these, it is preferable to use any metal element capable of having thermoelectric properties as an intermetallic compound (e.g., transition metal elements), with Mg, Al, Si, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Ge, Se, Zr, Nb, and Sn being more preferred.

[0032] From the viewpoint of improving thermoelectric properties, the intermetallic compound should preferably be a Heusler alloy represented by the compositional formula XY2Z, or a half-Heusler alloy represented by the compositional formula XYZ. The X atoms are, for example, one or more metallic elements selected from Ti, V, Cr, Mn, Y, Zr, Nb, Hf, and Ta. The Y atoms are, for example, one or more metallic elements selected from Fe, Co, Ni, Cu, Zn, Ru, Rh, Pd, Ag, Cd, Ir, Pt, and Au. The Z atoms are, for example, one or more metallic elements selected from Al, Si, Ga, Ge, As, In, Sn, Sb, Tl, Pd, Bi, Se, and Te. From the viewpoint of improving thermoelectric properties, it is preferable that the valence electron concentration (average number of valence electrons per atom) of the X, Y, and Z atoms is 6. As half-Heusler alloys, for example, TiNiSn, TiCoSb, and FeNbSb are preferred.

[0033] Furthermore, a portion of the intermetallic compound may be substituted with other metal elements.

[0034] As nanoceramics, one or more can be selected from oxides, carbides, nitrides, borides, and silicides of various metal elements. From the viewpoint of improving the heat resistance of the sintered body at high temperatures, oxides (oxide-based ceramics) are preferred among these.

[0035] Examples of oxides include Al2O3, ZrO2, MgO, La2O3, SiO2, TiO2, CeO2, ZnO, SnO2, UO2, Na2O·11Al2O3, 3Al2O3·2SiO2, and Y3Al5O 12 , BaTiO3, BaFe 12 O 19 And so on.

[0036] In particular, it is preferable to use an oxide that is more stable than the oxides of each element constituting the intermetallic compound (an oxide of an element with a stronger bond to oxygen than the metal element constituting the intermetallic compound) as the nanoceramic. For example, when the intermetallic compound is TiNiSn, oxides that are more stable than TiO2, NiO, and SnO2, such as Al2O3, MgO, La2O3, and ZrO2, can be used as nanoceramics.

[0037] Carbides include SiC, TiC, W2C, WC, and B4C. Nitrides include Si3N4, TiN, AlN, and SiAlON. Borides include TiB2, ZrB2, and LaB6. Silicides include MoSi2, FeSi2, and BaSi2.

[0038] Furthermore, the nanoceramics may be conductive as well as insulating. When using insulating nanoceramics, it is preferable to use nanoceramics with low thermal conductivity (for example, 50 W / m·K or less) from the viewpoint of not degrading the thermoelectric performance of the intermetallic compound powder.

[0039] The average particle size of the nanoceramics contained in the intermetallic compound powder is not particularly limited, but is, for example, 100 nm or less, preferably 50 nm or less, more preferably 20 nm or less, particularly preferably 10 nm or less, and most preferably 5 nm or less. The lower limit of the particle size of the nanoceramics is not particularly limited, but is, for example, 1 nm or more.

[0040] The ceramic content in the intermetallic compound powder is, for example, 0.5 vol% to 5.0 vol%, preferably 1.0 vol% to 4.0 vol%, relative to the total of the intermetallic compound and nanoceramics. Any known technique can be used to determine the ceramic content in the intermetallic compound powder. For example, quantitative analysis by X-ray diffraction (XRD), or compositional analysis or chemical bonding state analysis by energy-dispersive X-ray spectroscopy (EDX) or X-ray photoelectron spectroscopy (XPS) can be performed to determine the composition ratio (mixing ratio) of the intermetallic compound and ceramics, and then the ceramic content in the intermetallic compound powder can be determined by converting the respective density ratios to volume percentages (vol%).

[0041] The intermetallic compound powder mainly consists of an intermetallic compound phase in which nanoceramics are dispersed. The content of the intermetallic compound phase in the intermetallic compound powder is, for example, 93 vol% or more, preferably 95 vol% or more, and more preferably 98 vol% or more. If the intermetallic compound powder contains unavoidable impurities or unreacted metal elements, their content in the intermetallic compound powder is, for example, 7 vol% or less, preferably 5 vol% or less, and more preferably 2 vol% or less.

[0042] <Sintered body> This section describes a sintered body made of intermetallic compound powder (composite powder material). The sintered body according to the present invention is suitably used as a thermoelectric conversion element.

[0043] The properties of the sintered body of the present invention are, for example, as follows: Thermal conductivity (λ): 0.3~30 [W / mK] Electrical conductivity (σ or 1 / ρ): 50~50000 [S / cm] Seebeck coefficient (S): 10~500 [μV / K] Output factor: 0.1~20 [mW / mK] 2 ] Dimensionless figure of merit: 0.1~5

[0044] Thermal conductivity was determined by the laser flash method, electrical conductivity (electrical resistivity) by the four-terminal method, and Seebeck coefficient by the steady-state method. The output factor was S 2 The dimensionless index of performance is calculated using / ρ, and is S 2 The formula was calculated using T / ρλ. Here, S is the Seebeck coefficient, ρ is the electrical resistivity, T is the operating temperature, and λ is the thermal conductivity.

[0045] From the viewpoint of heat resistance, the sintered body according to the present invention has a weight change at 600°C, with 0°C as the reference (100%), of, for example, 100 to 100.2%, preferably 100 to 100.15%, and more preferably 100 to 100.1% in thermogravimetric measurements. The thermogravimetric measurements are performed in air at a heating rate of 10°C / min.

[0046] The nanoceramic content in the sintered body is, for example, 0.5 vol% to 5.0 vol%, preferably 1.0 vol% to 4.0 vol%, relative to the total of the intermetallic compound and nanoceramics (100 vol%). However, the lower limit of the nanoceramic content in the sintered body is not particularly limited and may be sufficiently smaller than 0.5 vol% (for example, 0.01 vol%).

[0047] Furthermore, during the heat treatment process for sintering, it is conceivable that the nanoceramics may substitute for some of the elements constituting the intermetallic compound, that the nanoceramics may form a new compound with the intermetallic compound, or that only the metal elements constituting the nanoceramics may remain in the sintered body.

[0048] Any known technique can be used to determine the nanoceramic content in a sintered body. For example, quantitative analysis by X-ray diffraction (XRD), or compositional analysis and chemical bonding state analysis by energy-dispersive X-ray spectroscopy (EDX) or X-ray photoelectron spectroscopy (XPS) can be performed to determine the composition ratio (mixing ratio) of intermetallic compounds and ceramics. The ceramic content in the sintered body can then be determined by converting the respective density ratios into volume percentages (vol%).

[0049] The sintered body typically consists mainly of intermetallic compound powder (for example, 95 vol% or more, preferably 98 vol% or more). However, other components besides intermetallic compound powder may be included in the sintered body as long as they do not impair the desired thermoelectric properties or effects. If other components are included, the content of these other components (such as impurities) in the sintered body should be, for example, less than 5 vol%, preferably less than 2 vol%.

[0050] From the viewpoint of heat resistance, the sintered body of the present invention is preferably a single phase containing an intermetallic compound and nanoceramics. In addition to being fine and homogeneous, the sintered body of the present invention also has good heat resistance.

[0051] <Method for producing intermetallic compound powder> The method for producing intermetallic compound powder according to the present invention generally involves adding nanoceramics powder to a metal raw material powder containing multiple metal elements and then grinding the mixture to produce the intermetallic compound powder. The production method of the present invention will be described in detail below.

[0052] (1) Production of metal raw material powder Metal raw material powder is a powder containing multiple (two or more) metal elements that constitute the desired intermetallic compound. As mentioned above in the section on <intermetallic compound powder>, the metal elements include not only the metal elements of groups 1 to 15 of the periodic table, but also metalloid elements.

[0053] First, the mixed powder is prepared by weighing and mixing metal powders containing the metal elements that make up the intermetallic compound. The amount of metal powder can be appropriately changed depending on the desired intermetallic compound.

[0054] Furthermore, as the metal powder, multiple types of metal powders (typically pure metal powders) containing each of two or more metal elements may be used, or alloy powders may be used as metal powders. For example, if one wants to obtain an intermetallic compound consisting of a first metal element, a second metal element, and a third metal element, one may use metal powders of the first metal element, metal powders of the second metal element, and metal powders of the third metal element, respectively, or one may use metal powders of an alloy consisting of the first and second metal elements, and metal powders of the third metal element.

[0055] The method of mixing each metal powder is arbitrary. For example, a mixed powder can be obtained by putting the metal powders into a container and mixing them using a rotating / revolving mixer.

[0056] Next, a molded body is obtained by molding the mixed powder. The method of molding the mixed powder is arbitrary. For example, the mixed powder can be molded by uniaxial pressure.

[0057] Then, the resulting molded body is heated to induce a solid-phase reaction. The molded body is heated, for example, at 200-2000°C in a vacuum for 5 minutes to 10 hours. The heated molded body is then pulverized to produce an intermetallic compound powder. The method of pulverizing the molded body is arbitrary. For example, the molded body can be pulverized by hand using a mortar and pestle to a size of approximately 0.5 mm or less.

[0058] Furthermore, the molded body after the solid-phase reaction contains unreacted metal elements and other phases (crystalline layers other than intermetallic compounds). Therefore, it is difficult to manufacture thermoelectric materials with desired thermoelectric properties from the molded body (sintered body) after the solid-phase reaction.

[0059] (2) Production of intermetallic compound powders The present invention relates to a method for producing intermetallic compound powder, which involves adding nanoceramics powder to a metal raw material powder and grinding it using a medium-stirring type pulverizer to produce the intermetallic compound powder.

[0060] A media-agitated pulverizer is a machine that produces powder by repeatedly compressing and pulverizing raw material powder by colliding it with a pulverizing medium. In this invention, in addition to metal raw material powder, nanoceramic powder is also fed into the media-agitated pulverizer.

[0061] Examples of media-agitated grinders include ball mills (e.g., rotary ball mills, vibratory ball mills, and planetary ball mills) and attritors, which use balls as the grinding medium. The grinding conditions are set appropriately according to the type of intermetallic compound powder desired. For example, metal raw material powder is ground at 50 to 2000 rpm for 1 to 10 hours in an atmosphere of air or an inert gas such as argon. The type and size of the grinding medium are arbitrary.

[0062] Grinding using a media-stirring pulverizer may be either dry or wet, using an organic solvent. However, dry grinding is preferred from the viewpoint of not degrading thermoelectric properties.

[0063] As for the nanoceramic powder, as described above for the <intermetallic compound powder>, one or more are selected from oxides, carbides, nitrides, borides, and silicides of various metal elements.

[0064] The average particle size of the nanoceramic powder is, for example, 100 nm or less, preferably 50 nm or less, and more preferably 20 nm or less, from the viewpoint of good dispersion in the intermetallic compound. The lower limit of the average particle size of the nanoceramics is not particularly limited, but is, for example, 1 nm or more. The average particle size refers to the particle size at 50% of the integrated value of the particle size distribution determined by laser diffraction-scattering (d50).

[0065] The average primary particle size of the nanoceramic powder is preferably, for example, 0.5 nm to 10 nm. The average primary particle size is the average value of the particle sizes measured for 30 or more arbitrarily selected primary particles during particle observation using an electron microscope (SEM or TEM).

[0066] If the amount of nanoceramic powder added is too small, the desired effect cannot be obtained, while if it is too large, the electrical resistivity of the intermetallic compound powder increases (i.e., the thermoelectric properties decrease). Therefore, the nanoceramic powder should be added in an amount of, for example, 0.5 vol% to 5.0 vol%, preferably 1.0 vol% to 4.0 vol%, relative to the total amount of metal raw material powder (total amount) and nanoceramic powder (100 vol%). However, if the nanoceramic powder is conductive, the amount of nanoceramic powder added is not limited to the above range.

[0067] In the method of producing intermetallic compound powder using a medium-stirring pulverizer without adding nanoceramic powder, sufficient pulverization and mixing of the metal raw material powder may not be possible due to aggregation accompanied by adhesion to the pulverization container and pulverization medium. Therefore, there is a problem in that fine and homogeneous intermetallic compound powder cannot be obtained. This problem is particularly pronounced when trying to obtain half-Heusler alloys such as TiNiSn that contain highly ductile elements.

[0068] In contrast, according to the method for producing intermetallic compound powder according to the present invention, by adding nanoceramic powder during grinding in a medium-stirring type grinder, aggregation accompanied by adhesion to the grinding container and grinding medium can be suppressed. Therefore, fine and homogeneous intermetallic compound powder can be obtained. Consequently, when the intermetallic compound powder is used as a thermoelectric material, good thermoelectric properties can be obtained. The production method in the present invention is particularly effective when obtaining intermetallic compound powder containing elements with high ductility.

[0069] Intermetallic compounds containing metal elements that form a hexagonal close-packed structure (hcp) (e.g., Ti, Zn, Co) or a face-centered cubic structure (fcc) (e.g., Ni, Ag, Pd) tend to aggregate and adhere easily, making pulverization by a media-stirred pulverizer difficult. Therefore, the method for producing intermetallic compound powder according to the present invention is particularly effective when using metal elements that form a hexagonal close-packed structure or a face-centered cubic structure.

[0070] Another method to suppress the aggregation of metal raw material powder during grinding in a media-agitated grinder involves adding organic solvents or lubricants. However, when intermetallic compound powders are used as thermoelectric materials, this is undesirable because it can lead to a decrease in thermoelectric properties due to compositional variations and the inclusion of impurities. In contrast, the present invention makes it possible to suppress the aggregation of metal raw material powder without adding organic solvents or lubricants. However, the method of grinding in a media-agitated grinder with the addition of organic solvents or lubricants is also included in the present invention.

[0071] Furthermore, there is a method of homogenizing intermetallic compound powder by heat treatment that lasts for tens of hours to several days. However, prolonged heat treatment consumes a huge amount of energy and is therefore undesirable from a practical standpoint. In contrast, the method for producing intermetallic compound powder according to the present invention has the advantage of being able to homogenize without prolonged heat treatment.

[0072] Another method to improve thermoelectric performance by reducing thermal conductivity is to replace some elements in the intermetallic compound with heavy elements. However, heavy elements such as Hf are expensive and rare, which poses a problem in terms of economic viability. In contrast, the present invention makes it possible to improve thermoelectric properties without replacing some elements in the intermetallic compound with heavy elements. However, the method of replacing some elements in the intermetallic compound with heavy elements is also included in the present invention.

[0073] As can be understood from the above description, a manufacturing method according to a preferred embodiment of the present invention includes a first step of causing a solid-phase reaction of multiple metal elements by heat treatment, and a second step of adding nanoceramics powder to the metal raw material powder containing the multiple metal elements after the solid-phase reaction and grinding it using a medium-stirring type pulverizer. That is, the metal raw material powder used in the second step is the powder after the solid-phase reaction of multiple metal elements.

[0074] In the manufacturing method of the present invention, the first step may be omitted. That is, in the second step, metal powder that has not undergone solid-phase reaction may be used as the metal raw material powder (for example, a mixed powder of metal powder containing a first metal element and metal elements containing a second metal element). However, from the viewpoint of significantly suppressing aggregation accompanied by adhesion to the grinding container and grinding medium, it is preferable to use powder containing multiple metal elements that have undergone solid-phase reaction as the metal raw material powder.

[0075] Furthermore, even when manufacturing alloy powders in general, including intermetallic compound powders, using a media-stirring type pulverizer, the problem of aggregation accompanied by adhesion can occur. Therefore, the method for producing intermetallic compound powder according to the present invention can also be applied to the production of alloy powders. It can also be specified as a method for producing alloy powder in which nanoceramics are dispersed in an alloy (e.g., interstitial / substitutional solid solution and intermetallic compound). The same effects as those described above for the method for producing intermetallic compound powder can be obtained with the above manufacturing method. Moreover, the alloy powder obtained by the above manufacturing method is homogeneous.

[0076] (3) Method for manufacturing a sintered body The method for manufacturing a sintered body according to the present invention includes a step of sintering an intermetallic compound powder (composite powder material). The sintered body according to the present invention is suitably used, for example, as a thermoelectric conversion element. The method for sintering the intermetallic compound powder is arbitrary. For example, the sintered body is manufactured by sintering in a vacuum at 500 to 1500°C for 5 to 10 minutes by energized pressurized sintering, where an electric current is applied while pressurizing.

[0077] Here, electrostatic pressure sintering has the advantage of producing a sintered body with a fine structure because it has a fast heating and cooling rate and sintering is performed under pressure. On the other hand, because the heating time is shorter than that of general sintering, it is difficult to obtain the effect of homogenizing the composition by thermal atomic diffusion. In other words, when sintering by electrostatic pressure sintering, it is necessary to use homogenized intermetallic compound powder. The intermetallic compound powder according to the present invention is sufficiently homogenized, so it has the advantage that a homogeneous sintered body can be obtained even when sintered by electrostatic pressure sintering. As can be understood from the above explanation, electrostatic pressure sintering can be effectively utilized with the intermetallic compound powder according to the present invention. However, methods for producing sintered bodies by sintering other than electrostatic pressure sintering are also included in the manufacturing method of the sintered body of the present invention.

[0078] Furthermore, when converting waste heat at high temperatures (e.g., about 600°C) into electrical energy, heat resistance in high-temperature air is desired for the thermoelectric conversion element. The sintered body obtained by sintering the intermetallic compound powder according to the present invention has the advantage of high heat resistance. Therefore, the sintered body of the present invention is also suitably used when converting waste heat at high temperatures into electrical energy. [Examples]

[0079] The present invention will be described in more detail below with reference to examples, but the present invention is not limited to these examples.

[0080] <Example 1-1> In Example 1-1, an intermetallic compound powder was prepared in which La2O3 was dispersed in TiNiSn (half-Heusler alloy).

[0081] (1) Production of metal raw material powder The metal raw material powder used in the intermetallic compound powder was manufactured as follows.

[0082] First, 1.28 g of Ti powder (purity: 99.9%), 1.56 g of Ni powder (purity: 99.9%), and 3.16 g of Sn powder (purity: 99.9%) were mixed. Specifically, the above metal powders (Ti powder, Ni powder, Sn powder) were placed in a plastic container (Mano Chemical UG container 24 ml) and mixed for 1 minute at 2000 rpm using a rotation-orbit mixer (Sinky Co., Ltd.: ARV-310P) to prepare the mixed powder.

[0083] Next, a molded body was manufactured by molding a mixed powder obtained by combining Ti powder, Ni powder, and Sn powder. The molded body was manufactured by uniaxial pressing (φ15 mm, 10 kN).

[0084] Next, the molded body of the mixed powder was heated. The molded body was heated in a magnesia crucible under vacuum at 1000°C (temperature increase / decrease 50°C / min) for 10 minutes. After heating, the molded body was manually crushed in a mortar to a size of 0.5 mm or less to obtain a TiNiSn metal raw material powder containing Ti, Ni, and Sn.

[0085] (2) Production of intermetallic compound powders Intermetallic compound powder was obtained by adding La2O3 powder (manufactured by Kanto Chemical Co., Ltd.: average particle size 15 nm or less, purity 99.95% or higher) to metal raw material powder and then grinding and mixing it using a planetary ball mill (manufactured by Fritsch: PL-7). The La2O3 powder was added at a concentration of 2 vol% relative to the total amount of metal raw material powder and La2O3 powder.

[0086] The grinding was performed using a planetary ball mill in a high-hardness stainless steel container (80 ml) at 200 rpm for 5 hours in an Ar atmosphere. 125 g of chromium steel grinding balls, each with a diameter of φ5, were used.

[0087] (3) Manufacturing of sintered bodies A sintered body was produced from 1.1 g of intermetallic compound powder by electrostatic pressure sintering. Electrostatic pressure sintering (φ10 graphite type) was performed in a vacuum at 1000°C (temperature rise / fall 100°C / min) for 10 minutes. The resulting sintered body was approximately φ10 mm in diameter and 2 mm thick.

[0088] <Example 1-2> In Example 1-2, TiNiSn in which a part of Sn in TiNiSn in Example 1-1 was replaced with Al 0.95 Al 0.05 was used, and it was the same as Example 1 except for this. TiNiSn 0.95 Al 0.05 was synthesized from 1.30 g of Ti powder, 1.60 g of Ni powder, 3.07 g of Sn powder, and 0.04 g of Al powder.

[0089] <Example 1-3> In Example 1-3, TiNiSn in which a part of Sn in TiNiSn in Example 1-1 was replaced with Sb 0.99 Sb 0.01 was used, and it was the same as Example 1 except for this. TiNiSn 0.99 Sb 0.01 was synthesized from 1.27 g of Ti powder, 1.56 g of Ni powder, 3.13 g of Sn powder, and 0.03 g of Sb powder. Note that Sb was added for the purpose of improving the conductivity in the sintered body.

[0090] <Example 1-4> Example 1-4 is TiNiSn in which only the ratio replaced with Sb is different from Example 1-3 0.98 Sb 0.02 was used. TiNiSn 0.98 Sb 0.02 was synthesized from 1.28 g of Ti powder, 1.56 g of Ni powder, 3.10 g of Sn powder, and 0.07 g of Sb powder.

[0091] <Comparative Example 1> Comparative Example 1 was the same as Example 1-1 except that La2O3 powder was not added in the production of the intermetallic compound powder.

[0092] <Example 2> In Example 2, an intermetallic compound powder in which Al2O3 was dispersed in FeNbSb (half Heusler alloy) was produced.

[0093] (1) Production of metal raw material powder The process for producing the metal raw material powder was the same as in Example 1, except that 1.24 g of Fe powder (purity: 99.9%), 2.06 g of Nb powder (purity: 99.9%), and 2.70 g of Sb powder (purity: 99.9%) were used.

[0094] (2) Production of intermetallic compound powders The procedure was the same as in Example 1, except that Al2O3 powder (manufactured by Sigma-Aldrich: average particle size 13 nm (TEM), purity 99.8%) was used instead of La2O3 powder. The Al2O3 powder was added at a concentration of 2 vol% relative to the total amount of metal raw material powder and Al2O3 powder.

[0095] (3) Manufacturing of sintered bodies A sintered body was obtained using the same method as in Example 1. <Comparative Example 2> Comparative Example 2 is the same as Example 2 except that Al2O3 powder was not added in the production of the intermetallic compound powder.

[0096] [evaluation] Example 1-1 and Comparative Example 1 were evaluated according to (1) to (6) below. Example 1-2 was evaluated according to (1), (5), and (6), Examples 1-3 and 1-4 were evaluated according to (1) and (5), and Example 2 was evaluated according to (1) and (2).

[0097] (1)Agglutination The inside of the high-hardness stainless steel container was visually observed after ball milling. In Comparative Examples 1 and 2, most of the metal raw material powder had aggregated and adhered to the inner surface of the container. In contrast, in Examples 1-1 to 1-4 and Example 2, adhesion to the inner surface of the container was largely eliminated, and no aggregation of the metal raw material powder was observed.

[0098] (2) Recovery rate The recovery rate of intermetallic compound powder produced from a planetary ball mill was calculated as follows. (Recovered intermetallic compound powder (g)) / (Metal raw material powder (g) + Nanoceramic powder (g)) × 100

[0099] The recovery rate for Comparative Example 1 was 87%. In contrast, the recovery rate for Example 1-1 was 96%. Example 1-1 showed a significant improvement in recovery rate compared to Comparative Example 1. The recovery rate for Comparative Example 2 was 95%. In contrast, the recovery rate for Example 2 was 96%. Example 2 also showed a slight improvement in recovery rate compared to Comparative Example 2. Note that for Comparative Example 1 and Comparative Example 2, the recovery rate was calculated including powder recovered by scraping off powder that had adhered to the inner surface of the container.

[0100] (3) Observation of fracture surface The fracture surfaces of the sintered bodies were observed using SEM (scanning electron microscope) images. Figure 1 shows SEM images for Comparative Example 1 and Example 1-1. As can be seen from Figure 1, the microstructure of Comparative Example 1 is observed to be heterogeneous. This is due to the fact that the grain growth rate differed in parts as a result of the uneven mixing of each metal element (Ti, Ni, Sn). Specifically, it is thought that grain growth was promoted in areas with a high concentration of low-melting-point Sn, while grain growth was slowed in areas with a low Sn concentration because the melting point became relatively higher.

[0101] In contrast, in Example 1-1, it was confirmed that a homogeneous microstructure was obtained. In Example 1-1, it is thought that grain growth was suppressed as a result of the uniform mixing of each metal element during grinding in the ball mill. This is presumed to be because grain growth was suppressed by the presence of nanoceramics at the grain boundaries in TiNiSn.

[0102] (4) X-ray diffraction measurement X-ray diffraction measurements were performed on the sintered bodies. Figure 2 shows the results of the X-ray diffraction measurements for Comparative Example 1 and Example 1-1. As can be seen from Figure 2, in Comparative Example 1, diffraction peaks indicating the Sn phase were observed in addition to the half-Heusler type TiNiSn phase. This suggests that the heterogeneity of the composition in the intermetallic compound powder remains in the sintered body. In contrast, in Example 1-1, no diffraction peaks indicating a second phase other than the TiNiSn phase were detected. This confirms that single-phase formation was achieved.

[0103] Here, because electrostatic pressure sintering is a short-time (minute-order) sintering process, a sintered body with a fine structure can be obtained. On the other hand, because the process is shorter than general sintering, it is difficult to obtain the effect of homogenizing the composition through thermal atomic diffusion. In Example 1-1, since single-phase formation was achieved, it is suggested that high homogenization was obtained despite the sintered body being manufactured by electrostatic pressure sintering.

[0104] (5) Thermoelectric properties For the sintered bodies of Examples 1-1 to 1-4 and Comparative Example 1, the power factor, dimensionless index of merit (ZT), electrical conductivity, Seebeck coefficient, and thermal conductivity were determined. The results are shown in Figures 3 to 5. Figure 3 shows the results for Example 1-1 and Comparative Example 1, Figure 4 shows the results for Example 1-2 and Comparative Example 1, and Figure 5 shows the results for Examples 1-3, 1-4 and Comparative Example 1. The methods for determining the power factor, dimensionless index of merit, electrical conductivity, Seebeck coefficient, and thermal conductivity are as described above.

[0105] First, let's focus on Examples 1-1 and 1-2. As can be seen from Figures 3 and 4, Comparative Example 1 showed high conductivity due to the deposition of the Sn phase, but its Seebeck coefficient was low. In contrast, Examples 1-1 and 1-2, while inferior in conductivity compared to Comparative Example 1, showed that they obtained the inherently high Seebeck coefficient due to the pseudogap electronic structure of the half-Heusler phase (TiNiSn phase). As a result, Examples 1-1 and 1-2 showed a significant improvement in the power factor (an index that evaluates thermoelectric performance using only the electrical components) compared to Comparative Example 1. Furthermore, in Example 1, the thermal conductivity was lower compared to Comparative Example 1 due to the homogenization of the composition and the removal of coarse structures. From these results, Examples 1-1 and 1-2 showed an improvement of approximately 1.5 to 2 times in the dimensionless figure of merit ZT, which represents the overall thermoelectric performance, compared to Comparative Example 1.

[0106] As described above, in Examples 1-1 and 1-2, the homogenization effect of adding nanoceramic powder during the grinding process in the planetary ball mill is thought to have stabilized the Heusler structure in the intermetallic compound, thereby improving the orderliness of the crystal structure. As a result of this improved orderliness of the crystal structure, the Seebeck coefficient increased. Therefore, the thermoelectric performance improved.

[0107] Next, let's look at Examples 1-3 and 1-4. As can be seen from Figure 5, the conductivity in Examples 1-3 and 1-4 was significantly improved compared to Comparative Example 1 (and even Examples 1-1 and 1-2). As a result of the significant improvement in conductivity in Examples 1-3 and 1-4, the power factor also improved. And, along with the improvement in the power factor, the dimensionless figure of merit ZT also improved. As can be understood from the above explanation, it was confirmed that the thermoelectric performance was improved by substituting some of the Sn in TiNiSn with Sb.

[0108] In Examples 1-3 and 1-4, the amount of Sb powder added during grinding in the planetary ball mill to improve the conductivity of the sintered body was very small. Given that the amount of Sb powder added was very small, if the Sb powder is not uniformly mixed during grinding in the planetary ball mill, the doping effect of Sb will not be obtained. And if the doping effect of Sb is not obtained, it can be inferred that the conductivity will be about the same as in Examples 1-1 and 1-2. In contrast, Examples 1-3 and 1-4 showed significantly higher conductivity compared to Examples 1-1 and 1-2. That is, it can be said that the Sb powder was uniformly mixed during grinding in the planetary ball mill in Examples 1-3 and 1-4.

[0109] As described above, in Examples 1-3 and 1-4, the addition of nanoceramic powder during the grinding process of the planetary ball mill resulted in homogenization (i.e., homogeneous dispersion of Sb), which allowed Sb to exert the desired doping effect. As a result of Sb exerting the desired doping effect, conductivity improved. Therefore, thermoelectric performance improved.

[0110] (6) Thermogravimetry Thermogravimetric analysis was performed in air on the sintered bodies according to Examples 1-1, 1-2, and Comparative Example 1. Figures 6 and 7 show the results. As can be seen from Figures 6 and 7, in Comparative Example 1, an increase in weight was observed from a relatively low temperature of 200 to 300°C. In Comparative Example 1, the weight change at 600°C, with 0°C as the baseline, exceeded 100.2% in thermogravimetric analysis. This suggests that thermally reactive parts such as the Sn phase were oxidized.

[0111] In contrast, in Examples 1-1 and 1-2, almost no weight increase was observed up to approximately 600°C. That is, it was confirmed that a sintered body exhibiting the inherently high heat resistance of the TiNiSn phase was obtained. Specifically, in Examples 1-1 and 1-2, the weight change at 600°C, with 0°C as the reference temperature, was approximately 100.05% in thermogravimetric measurements. As can be understood from the above explanation, the sintered body made of intermetallic compound powder according to the present invention is also suitably used when converting waste heat at high temperatures (for example, about 600°C) into electrical energy.

Claims

1. The process includes adding nanoceramics powder to a metal raw material powder containing multiple metal elements and grinding it using a medium-stirring type pulverizer. The nanoceramics powder is added in an amount of 0.5 vol% to 5.0 vol% relative to the total amount of the metal raw material powder and the nanoceramics powder. A method for producing intermetallic compound powder.

2. The process includes adding nanoceramics powder to a metal raw material powder containing multiple metal elements and grinding it using a medium-stirring type pulverizer. The aforementioned nanoceramic powder is La ２ O ３ including A method for producing intermetallic compound powder.

3. The average particle size of the nanoceramic powder is 100 nm or less. A method for producing intermetallic compound powder according to claim 1 or 2.

4. The aforementioned nanoceramic powder is an oxide-based ceramic. A method for producing intermetallic compound powder according to claim 1.

5. The aforementioned oxide ceramics are Al ２ O ３ MgO, La ２ O ３ and ZrO ２ One or more selected from A method for producing intermetallic compound powder according to claim 4.

6. The aforementioned metal raw material powder is a powder obtained after a solid-phase reaction of the plurality of metal elements. A method for producing intermetallic compound powder according to claim 1 or 2.

7. The process includes a step of sintering a composite powder material in which nanoceramics are dispersed in an intermetallic compound. The composite powder material is an intermetallic compound powder produced by the manufacturing method of claim 1 or claim 2. A method for producing intermetallic compound sintered bodies.

8. In the above process, the composite powder material is sintered by electrostatic pressure sintering. A method for producing an intermetallic compound sintered body according to claim 7.

9. This is a sintered body of an intermetallic compound powder, which is a composite powder material in which nanoceramics are dispersed in an intermetallic compound. In thermogravimetric measurements, the weight change at 600°C, relative to 0°C, is 100-100.2%. Intermetallic compound sintered body.

10. A thermoelectric conversion element made of an intermetallic compound sintered body according to Claim 9.

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