Patent Application
20200269314
Embodiments of the present invention relate to a boron-nitride nanoplatelet(s) (BNNP)/metal nanocomposite powder and a preparing method thereof.
Metals are materials with excellent strengths and excellent thermal and electrical conductivities. Further, due to great ductility, metals are relatively easy to process when compared to other materials and thus, are applied throughout industries for multiple purposes. In recent years, studies have been conducted actively to prepare metal nanocomposite powders having high industrial applicability by incorporating nanotechnology into metals.
In the study of metal nanocomposite powders, in addition to properties of metals, mechanical properties newly emerging as the particle size of the metals becomes finer attract attention. In particular, various functionalities expected by nanomaterials in addition to metal particles may be additionally secured. Thus, new properties caused by inter-particle interactions, volume effects, and surface effects are expected to be applied to high-temperature structural materials, tool materials, electromagnetic materials, filters, and sensors as advanced materials.
In such metal nanopowders, studies have been conducted to add new functions while maintaining properties of the existing metal powders or to improve mechanical and electrical properties of the existing metal powders. In particular, there is a growing interest in composite powder materials with improved mechanical and electrical properties when compared to the existing metal powders by dispersing inorganic materials.
In recent years, studies have been conducted by utilizing carbon-based nanomaterials such as graphene or carbon nanotubes (CNT), in metal nanocomposite materials among various materials. However, such carbon-based nanomaterials have relatively low stabilities at high temperature, and the nanomaterials themselves have significantly low expected physical properties due to functional grouping and many defects occurring in the preparing process. Thus, there is an increasing demand for a new material applicable as a reinforcement to solve the foregoing issues.
Technical Goals
An aspect of the present invention provides a boron-nitride nanoplatelet(s) (BNNP)/metal nanocomposite powder to which BNNP are applied.
An aspect of the present invention provides a method of preparing the BNNP/metal nanocomposite powder.
According to an aspect of the present invention, there is provided a boron-nitride to nanoplatelet(s) (BNNP)/metal nanocomposite powder including a base metal, and BNNP dispersed in the base metal and configured to serve as a reinforcement of the base metal, wherein the BNNP may be interposed between metal particles of the base metal in the form of a thin film of a plurality of layers and combined with the metal particles, and an amount of the BNNP in the base metal may be greater than 0 vol % and less than 90 vol %.
The metal particles may have the size of 1 nm to 50 μm.
The BNNP may have the thickness of 0.5 nm to 100 nm and the size of 1.5 μm to 10 μm.
The base metal may include at least one of alkali metals, alkaline earth metals, transition metals, post-transition metals, and metalloids.
According to an aspect of the present invention, there is provided a method of preparing a BNNP/metal nanocomposite powder, the method including acquiring a nanocomposite powder by dispersing a BNNP powder within a base metal.
The base metal may include at least one of alkali metals, alkaline earth metals, transition metals, post-transition metals, and metalloids.
The acquiring may include dispersing BNNP into a solvent, providing a metal salt to be applied as the base metal to the BNNP-dispersed solvent, and forming a powder in which the BNNP are dispersed in the form of a thin film of a plurality of layers between metal particles of the base metal by reducing the BNNP and the metal salt.
The forming may include returning the BNNP functional group material and the metal salt together with a reduction atmosphere or a reducer.
The acquiring may include dispersing BNNP into a solvent, providing a metal salt to be applied as the base metal to the BNNP-dispersed solvent, forming a metallic oxide by oxidizing the metal salt in the solvent, and forming a powder in which the BNNP are dispersed in the form of a thin film of a plurality of layers between metal particles of the base metal by reducing the BNNP and the metallic oxide.
The forming of the metallic oxide may include performing a heat treatment after providing an oxidizer to the solvent including the BNNP and the metal salt.
The forming of the powder may include performing a heat treatment on a composite powder including the BNNP and the metallic oxide in a reduction atmosphere.
The method may further include forming a bulk material by sintering a BNNP/metal nanocomposite powder obtained during the acquiring of the nanocomposite powder at room temperature to a temperature of 90% of a melting point of the base metal.
It should be understood that effects achievable through embodiments set forth herein are not limited to the above effects and include all effects that can be deduced from the configuration described in the following description or the scope of the claims.
According to embodiments, it is possible to provide a boron-nitride nanoplatelet(s) (BNNP)/metal nanocomposite powder with improved mechanical strength, electrical conductivity, or thermal conductivity by dispersing BNNP as a reinforcement in a base metal.
According to embodiments, it is possible to uniformly disperse BNNP in a base material including an alloy or nano-metal particles through molecular level or mechanical milling, and to provide a BNNP/metal nanocomposite powder with enhanced mechanical properties when compared to the existing metals or alloys.
Hereinafter, examples will be described in detail with reference to the accompanying drawings. However, various alterations and modifications may be made to the examples. Here, the examples are not construed as limited to the disclosure and should be understood to include all changes, equivalents, and replacements within the idea and the technical scope of the disclosure.
The terminology used herein is for the purpose of describing particular examples only and is not to be limiting of the examples. As used herein, the singular forms “a”, “an”, and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise. It will be further understood that the terms “comprises/comprising” and/or “includes/including” when used herein, specify the presence of stated features, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, integers, steps, operations, elements, components and/or groups thereof.
Unless otherwise defined, all terms including technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which examples belong. It will be further understood that terms, such as those defined in commonly-used dictionaries, should be interpreted as having a meaning that is consistent with their meaning in the context of the relevant art and will not be interpreted in an idealized or overly formal sense unless expressly so defined herein.
When describing the examples with reference to the accompanying drawings, like reference numerals refer to like constituent elements and a repeated description related thereto will be omitted. In the description of examples, detailed description of well-known related structures or functions will be omitted when it is deemed that such to description will cause ambiguous interpretation of the present disclosure.
According to an embodiment, there is provided a boron nitride nanoplatelet(s) BNNP/metal nanocomposite powder which includes a base metal and a reinforcement dispersed in the base metal and may provide improved mechanical, electrical, and thermal properties.
The reinforcement may include BNNP. The BNNP is a material having a hexagonal system structure, in which boron atoms and nitrogen atoms are provided in a planar two-dimensional (2D) hexagonal structure, the material with high physical and chemical stability. Further, the BNNP has excellent mechanical and thermal properties and thus, has an excellent thermal stability at high temperature. For example, the BNNP is stable up to 3000° C. in an inert atmosphere, has a high thermal shock resistance due to its thermal conductivity as high as that of stainless steel, is not cracked or damaged despite of repetition of rapid heating and rapid cooling of about 1500° C., and has excellent high-temperature lubricative characteristic and corrosion resistance. In addition, due to the characteristics described above, the BNP may be applied as a reinforcement to improve properties of a nanocomposite powder. For example, the BNNP may be interposed between metal particles of the base metal in the form of a thin film of a plurality of layers and combined with the metal particles, thereby improving the properties of the nanocomposite powder.
The BNNP may be included within a range which may prevent a structural deformation caused by a reaction between the BNNP within the base metal. For example, an amount of the BNNP in the base metal may be greater than 0 vol % and less than 90 vol %.
The BNNP may include a plurality of layers, preferably, 3 to 10 layers to reduce a structural defect and an interfacial resistance. Further, the BNNP may have various forms, for example, the form of a thin film.
The BNNP may have the thickness of 0.5 nm to 100 nm and the size of 1.5 μm to 10 μm, and if included in the thickness and size range, the BNNP may be dispersed well in the base metal, whereby the nanocomposite powder with improved mechanical strength, electrical conductivity, and thermal conductivity may be provided.
The metal particles may include at least one of alkali metals, alkaline earth metals, transition metals, post-transition metals, and metalloids. For example, the metal particles may include at least one of nickel, cobalt, molybdenum, iron, potassium, ruthenium, chromium, gold, silver, aluminum, magnesium, titanium, tungsten, lead, zirconium, zinc, and platinum. Further, the metal particles may be an alloy including at least one of the above-mentioned metals, for example, SUS400 series stainless steel, ASTM 52100, SUJ-2, or in detail, SUS400C.
The metal particles may have the size of 1 nm to 50 μm, and the size may be the diameter, the length, the thickness, or the height depending on the form of the particles.
The BNNP/metal nanocomposite powder may provide improved mechanical properties of about 101 to 200% of the young's modulus, 101 to 300% of the yield strength, and 101 to 200% of the tensile strength, when compared to a pure base metal.
According to an embodiment, there is provided a method of preparing a BNNP/metal nanocomposite powder, in detail, the method including acquiring a nanocomposite powder by dispersing a BNNP powder within a base metal.
In the method, the dispersed BNNP may serve as a reinforcement of the base metal, and the dispersed BNNP may be controlled to be greater than 0 vol % and less than 90 vol %.
The acquiring of the nanocomposite powder may be performed using a mechanical mixing process and a molecular level mixing process. When the mechanical mixing process is used, the acquiring of the nanocomposite powder may include preparing a base metal powder, and mixing the BNNP powder and the base metal powder using a ball mill.
In the preparing of the base metal powder, the base metal may be a metal or an alloy including at least one of alkali metals, alkaline earth metals, transition metals, post-transition metals, and metalloids.
The BNNP powder to be applied as a reinforcement of the nanocomposite powder may be prepared and used, and the preparing of the base metal powder may include, for example, forming a slurry by mixing hexagonal boron nitride (h-BN) particles and a NaOH aqueous solution, ball-milling the slurry using a stainless steel ball, removing impurities by adding an acid to the slurry and performing a sonication thereon, and acquiring a solid from the slurry and washing the solid after the removing of the impurities. The removing of the impurities may be performed using an acid or an acidic aqueous solution including at least one of nitric acid, hydrochloric acid, sulfuric acid, and acetic acid.
The mixing of the BNNP powder and the base metal powder using the ball mill may be performed by mixing the powder through ball milling for 1 to 10 hours at 50 rpm or higher, 50 rpm to 500 rpm, or 10 rpm to 200 rpm, wherein a mixing ratio (w/w) of the stainless ball:the whole powder may be 50:0.5 to 2.
When the molecular level mixing process is used, the acquiring of the nanocomposite powder may include dispersing BNNP into a solvent, providing a metal salt to be applied as the base metal to the BNNP-dispersed solvent, and forming a powder in which the BNNP are dispersed in the form of a thin film of a plurality of layers between metal particles of the base metal by reducing the BNNP and the metal salt.
In the providing of the metal salt, the metal salt may include at least one of carbonates, chlorides, fluorides, nitrates, sulphates, nitrates, and oxalates.
The forming of the powder in which the BNNP are dispersed may be returning the BNNP functional group material and the metal salt together with a reduction atmosphere or a reducer. The reduction atmosphere may include at least one reducing gas of hydrogen (H2), hydrocarbons (CH4), and carbon monoxide (CO), and the forming of the powder in which the BNNP are dispersed may be performed for 30 minutes to 10 hours at a temperature of 100° C. or higher, or 100° C. to 500° C. in a reduction atmosphere in which the reducing gas and an inert gas such as Ar or He are mixed.
When the molecular level mixing process is used, the acquiring of the nanocomposite powder may include dispersing BNNP into a solvent, providing a metal salt to be applied as the base metal to the BNNP-dispersed solvent, forming a metallic oxide by oxidizing the metal salt in the solvent, and forming a powder in which the BNNP are dispersed in the form of a thin film of a plurality of layers between metal particles of the base metal by reducing the BNNP and the metallic oxide.
The forming of the metallic oxide may be performing a heat treatment after providing an oxidizer to the solvent including the BNNP and the metal salt. The forming of the metallic oxide may be performed by performing a heat treatment for 30 minutes to hours at a temperature of 100° C. to 500° C. after providing the oxidizer. The oxidizer may include NaOH, KOH, or both.
The method may further include forming a bulk material, and the forming of the bulk material may be forming the bulk material by sintering a BNNP/metal nanocomposite powder obtained during the acquiring of the nanocomposite powder at room temperature to a temperature of 90% of a melting point of the base metal.
The room temperature to the temperature of 90% of the melting point of the base material may be room temperature to 2000° C., or 100° C. to 1000° C., and the sintering may be performed for 1 minute or longer, 1 minute to 30 minutes, or 1 minute to 20 minutes at the above temperature. If included in the temperature and time range, an appropriate combination of the base metal and the BNNP may be induced, and a nanocomposite material with improved mechanical and thermal properties may be provided. Further, the sintering of the powder may be performed by heating the powder at a heating rate of 50 to 200° C./min.
Synthesis of BNNP
A slurry was prepared by mixing 2 g of h-BN (hexagonal boron nitride) particles and 20 ml of an NaOH aqueous solution (concentration: 2 M), and ball-milled (50:1 ball to powder ratio, 100 g SUS ball) at 200 rpm and for 24 hours. Then, the slurry was filled with 800 mL of distilled water, 200 mL of HCl was added, and impurities were removed by performing a sonication. A solid of the slurry was filtered, washed with water, then dispersed again by performing a sonication in IPA for 1 hour, centrifuged at 2000 rpm and for 30 minutes, filtered, and dried. Transmission Electron Microscope (TEM) images of the obtained BNNP are shown in
Preparation of Nanocomposite Powder
An aqueous dispersion of BNNP was prepared by dispersing the BNNP obtained in Preparation Example in distilled water, and mixed with a Cu(II) acetate aqueous solution. Then, a composite powder of copper oxide and BNNP was formed by adding NaOH to the mixture and oxidizing the same at 80° C. The powder was filtered in a vacuum and washed. Then, a reducing process was performed at a temperature of 450° C. and for 3 hours in a reducing furnace of an H2 gas atmosphere, whereby 1, 1.5, 2, 2.5 and 3 vol % BNNP/Cu nanocomposite powders were obtained respectively.
Sintering of Nanocomposite Powder
The BNNP/Cu nanocomposite powder was sintered through spark plasma sintering at 950° C. and for 5 minutes. An image and a Scanning Electron Microscope (SEM) image of the powder sintered body are illustrated in
Preparation of Nanocomposite Powder
BNNP (235.5 mg) and 29.746 g of SUS440C powder (particle size: 1-50 um) were mixed and ball-milled (50:1 ball to powder ratio, 100 g SUS ball) at 100 rpm and for 1 hour. Then, a BNNP/SUS440C nanocomposite powder was acquired.
Sintering of Nanocomposite Powder
The BNNP/SUS440C nanocomposite powder was sintered through spark plasma sintering at 950° C. and for 5 minutes, as in Example 1.
In the same manner as in Example 1, except that graphene was applied, a 3 vol % graphene/Cu nanocomposite powder was obtained and sintered.
Electrical Property Evaluation
The sintered bodies of the 3 vol % graphene/Cu nanocomposite powder of Comparative Example 1 and the 3 vol % BNNP/Cu nanocomposite powder of Example 1 were used, and electrical properties thereof were measured using a 4-point probe after polishing the sintered bodies to the thickness of 1 um.
(2) Thermal Conductivity Evaluation
Thermal conductivities of respective specimens in different grain sizes were measured by growing gains. Corresponding results are shown in
Further, in a large grain size, the specimen of the composite powder (3 vol %) of Example 1 shows a loss of 3%, whereas the graphene/Cu specimen shows a loss of 17%. That is, a decrease in the interfacial resistance may be induced by relatively fewer functions groups when compared to graphene by addition of BNNP, whereby the thermal conductivity may improve.
(2) Electrical Conductivity Evaluation
Electrical conductivities of respective specimens in different grain sizes were measured by growing grains. Corresponding results are shown in Table 1 and
Referring to Table 1 and
(3) Mechanical Property Evaluation
Specimens were prepared by modeling the 3 vol % BNNP/Cu nanocomposite powder of Example 1 and the 1 vol % BNNP/Cu nanocomposite powder and a powder of pure Cu into pellets and then performing spark plasma sintering thereon at 950° C. and for 5 minutes. Stresses and strains were measured and shown in Table 2 and
Referring to Table 2 and
(4) Wear Resistance Evaluation
A wear resistance of the sintered body according to Example 1 was evaluated under the condition of load: 30 kg·f, distance: 1000 m, and counter material: WC-Co. and corresponding results are shown in
Referring to
Specimens respectively with the height of 7.71 mm and 6.89 mm were prepared using the SUS440C and the sintered body of the BNNP/SUS440C nanocomposite powder of Example 2, and wear resistances thereof were evaluated under the condition of load: kg·f, distance: 500 m, and counter material: SKD, and corresponding results are shown in
In
A number of example embodiments have been described above. Nevertheless, it should be understood that various modifications may be made to these example embodiments. For example, suitable results may be achieved if the described techniques are performed in a different order and/or if components in a described system, architecture, device, or circuit are combined in a different manner and/or replaced or supplemented by other components or their equivalents.
Accordingly, other implementations are within the scope of the following claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2018-0042691 | Apr 2018 | KR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/KR2019/000954 | 1/23/2019 | WO | 00 |
