WO2022137949A1 - 酸化物複合粒子及びその製造方法、並びに樹脂組成物 - Google Patents

酸化物複合粒子及びその製造方法、並びに樹脂組成物 Download PDF

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WO2022137949A1
WO2022137949A1 PCT/JP2021/042902 JP2021042902W WO2022137949A1 WO 2022137949 A1 WO2022137949 A1 WO 2022137949A1 JP 2021042902 W JP2021042902 W JP 2021042902W WO 2022137949 A1 WO2022137949 A1 WO 2022137949A1
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oxide composite
mass
composite particles
particles
resin composition
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English (en)
French (fr)
Japanese (ja)
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俊彦 恒吉
元晴 深澤
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Denka Co Ltd
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Denka Co Ltd
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Priority to JP2022571985A priority Critical patent/JP7756658B2/ja
Priority to CN202180087016.9A priority patent/CN116648429A/zh
Priority to EP21910102.9A priority patent/EP4269343A4/en
Priority to US18/269,481 priority patent/US20240076470A1/en
Priority to KR1020237024661A priority patent/KR20230122641A/ko
Publication of WO2022137949A1 publication Critical patent/WO2022137949A1/ja
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/34—Silicon-containing compounds
    • C08K3/36—Silica
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/16—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on silicates other than clay
    • C04B35/18—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on silicates other than clay rich in aluminium oxide
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B33/00—Silicon; Compounds thereof
    • C01B33/113—Silicon oxides; Hydrates thereof
    • C01B33/12—Silica; Hydrates thereof, e.g. lepidoic silicic acid
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B33/00—Silicon; Compounds thereof
    • C01B33/113—Silicon oxides; Hydrates thereof
    • C01B33/12—Silica; Hydrates thereof, e.g. lepidoic silicic acid
    • C01B33/18—Preparation of finely divided silica neither in sol nor in gel form; After-treatment thereof
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B33/00—Silicon; Compounds thereof
    • C01B33/20—Silicates
    • C01B33/26—Aluminium-containing silicates, i.e. silico-aluminates
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
    • C01F7/00—Compounds of aluminium
    • C01F7/02—Aluminium oxide; Aluminium hydroxide; Aluminates
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
    • C08K3/013—Fillers, pigments or reinforcing additives
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20—Oxides; Hydroxides
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20—Oxides; Hydroxides
    • C08K3/22—Oxides; Hydroxides of metals
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2002/00—Crystal-structural characteristics
    • C01P2002/80—Crystal-structural characteristics defined by measured data other than those specified in group C01P2002/70
    • C01P2002/85—Crystal-structural characteristics defined by measured data other than those specified in group C01P2002/70 by XPS, EDX or EDAX data
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00—Particle morphology
    • C01P2004/60—Particles characterised by their size
    • C01P2004/61—Micrometer sized, i.e. from 1-100 micrometer
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00—Particle morphology
    • C01P2004/80—Particles consisting of a mixture of two or more inorganic phases
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20—Oxides; Hydroxides
    • C08K3/22—Oxides; Hydroxides of metals
    • C08K2003/2227—Oxides; Hydroxides of metals of aluminium
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00—Specific properties of additives
    • C08K2201/002—Physical properties
    • C08K2201/003—Additives being defined by their diameter

Definitions

  • the present invention relates to oxide composite particles, a method for producing the same, and a resin composition.
  • silica As a high-frequency band ceramic material, silica (SiO 2 ) has a small dielectric constant (3.7), a quality coefficient index Qf (value obtained by multiplying the inverse of the dielectric loss tangent and the measurement frequency) of about 120,000, and is low in dielectric. It is promising as a material for fillers having a high rate and low dielectric loss tangent. Further, in order to facilitate compounding in the resin, it is preferable that the filler shape is closer to a spherical shape. Spherical silica can be easily synthesized (for example, Patent Document 1) and has already been used in many applications. Therefore, it is expected to be widely used in high frequency band dielectric devices and the like.
  • the spherical silica is generally amorphous, has a low thermal conductivity of about 1 W / m ⁇ K, and the resin composition filled with the spherical silica may have insufficient heat dissipation.
  • Patent Documents 2 and 3 propose that amorphous spherical silica is crystallized into quartz or cristobalite by heat treatment.
  • Patent Document 4 discloses a silica powder having a film made of an aluminum oxide-based ceramic formed by using Aerosil.
  • Japanese Unexamined Patent Publication No. 58-138740 Japanese Patent No. 6207753 International Publication No. 2018/186308 Japanese Unexamined Patent Publication No. 10-251042
  • An object of the present invention is to provide an oxide composite particle in which a resin composition obtained by mixing with a resin exhibits high thermal conductivity, low dielectric constant and dielectric loss tangent, a method for producing the same, and the resin composition. And.
  • the present invention includes the following embodiments.
  • Oxide composite particles containing silica and alumina contain 40 to 85% by mass of the crystal phase of ⁇ -cristobalite, 5 to 50% by mass of the crystal phase of ⁇ -alumina, and 10% by mass or less of the crystal phase ofnite.
  • [5] The method for producing an oxide composite particle according to any one of [1] to [4].
  • a resin composition containing the oxide composite particles according to any one of [1] to [4] and a resin is a resin composition containing the oxide composite particles according to any one of [1] to [4] and a resin.
  • the resin composition obtained by mixing with a resin provides oxide composite particles having high thermal conductivity, low dielectric constant and dielectric loss tangent, a method for producing the same, and the resin composition. Can be done.
  • FIG. 1 It is a figure which shows the X-ray diffraction pattern of the oxide composite particle of Example 1.
  • FIG. 1 shows the X-ray diffraction pattern of the oxide composite particle of Example 1.
  • the oxide composite particles according to this embodiment include silica and alumina.
  • the oxide composite particles contain 40 to 85% by mass of the crystal phase of ⁇ -cristobalite, 5 to 50% by mass of the crystal phase of ⁇ -alumina, and 10% by mass or less of the crystal phase ofnite.
  • the element ratio (aluminum / silicon) of aluminum to silicon, which is detected by X-ray photoelectron spectroscopy (hereinafter, also referred to as XPS) is 1.5 or more.
  • the oxide composite particles according to the present embodiment have a high thermal conductivity in the resin composition by containing the crystal phase of ⁇ -Christovalite, the crystal phase of ⁇ -alumina, and the crystal phase of mullite within the above-mentioned contents. , And low dielectric constant and dielectric tangent can be achieved.
  • the oxide composite particles according to the present embodiment have an element ratio of aluminum / silicon detected by XPS of 1.5 or more, a large amount of alumina is present on the surface of the oxide composite particles, and the oxide composite particles are present. It has a structure in which at least a part of the surface of the surface is covered with an alumina layer.
  • the alumina layer located on the surface of the oxide composite particles exhibits high thermal conductivity, and the crystal phase of ⁇ -Christovalite contained in the oxide composite particles exhibits a low dielectric constant and dielectric loss tangent, so that the whole is as a whole. High thermal conductivity, as well as low permittivity and dielectric loss tangent can be achieved.
  • the oxide composite particles contain 40 to 85% by mass of the crystal phase of ⁇ -Christovalite, based on the mass of the entire oxide composite particles (that is, the mass of the entire oxide composite particles is 100% by mass).
  • the content of the crystal phase of ⁇ -cristobalite is less than 40% by mass, the dielectric constant and the dielectric loss tangent become large, and it becomes difficult to use it in a high frequency device. Further, when the content exceeds 85% by mass, the thermal conductivity of the resin composition cannot be guaranteed.
  • the content can be, for example, 50 to 85% by mass, 60 to 85% by mass, 70 to 85% by mass, and 75 to 85% by mass.
  • the crystal phase is identified and quantified by the powder X-ray diffraction / Rietveld method. Attribution of crystals can be performed, for example, in an X-ray database or the like. Specifically, it can be analyzed by a method described later.
  • the oxide composite particles contain 5 to 50% by mass of the crystal phase of ⁇ -alumina based on the mass of the entire oxide composite particles (that is, the mass of the entire oxide composite particles is 100% by mass).
  • the content of the crystal phase of ⁇ -alumina is less than 5% by mass, the thermal conductivity of the resin composition cannot be guaranteed. Further, when the content exceeds 50% by mass, the dielectric constant and the dielectric loss tangent become large, which makes it difficult to use for a high frequency device.
  • the content can be, for example, 10-50% by mass, 10-40% by mass, 10-30% by mass, 10-25% by mass, and so on. It can be 10 to 20% by mass.
  • the identification, quantification, and crystal attribution of the crystal phase can be performed by the same method as the above-mentioned ⁇ -cristobalite crystal phase. Specifically, it can be analyzed by a method described later.
  • the oxide composite particles contain 10% by mass or less of the crystal phase of mullite based on the total mass of the oxide composite particles (that is, the total mass of the oxide composite particles is 100% by mass).
  • the content of the crystal phase of Murite exceeds 10% by mass, the dielectric properties such as the dielectric constant and the dielectric loss tangent and the heat conduction performance are slightly deteriorated.
  • the content of the crystal phase of mullite can be 5% by mass or less, and can be 1% by mass or less.
  • the lower limit of the content of the crystal phase of mullite is not particularly limited, but may be, for example, 0.01% by mass or more.
  • the oxide composite particles according to this embodiment do not have to contain the crystal phase of mullite.
  • the identification, quantification, and crystal attribution of the crystal phase can be performed by the same method as the above-mentioned ⁇ -cristobalite crystal phase. Specifically, it can be analyzed by a method described later.
  • the oxide composite particles can contain 50% by mass or less of amorphous silica based on the total mass of the oxide composite particles (that is, the total mass of the oxide composite particles is 100% by mass). It is preferably contained in an amount of 0.01 to 15% by mass, more preferably 0.01 to 5% by mass. When the content of amorphous silica is 50% by mass or less, the value of dielectric loss tangent can be kept low.
  • the oxide composite particles according to this embodiment do not have to contain amorphous silica.
  • the identification and quantification of amorphous silica can be performed by the same method as the above-mentioned crystal phase of ⁇ -cristobalite. Specifically, it can be analyzed by a method described later.
  • the oxide composite particles may contain other crystal phases or other amorphous phases. Further may be included. Examples of other crystal phases include ⁇ -alumina, ⁇ -alumina, quartz and the like. Examples of other amorphous phases include alumina and the like.
  • the content of the other crystal phase can be, for example, 0 to 8% by mass based on the total mass of the oxide composite particles (that is, the total mass of the oxide composite particles is 100% by mass). It can be 0 to 4% by mass.
  • the content of the other amorphous phase is, for example, 0 to 8% by mass based on the total mass of the oxide composite particles (that is, the total mass of the oxide composite particles is 100% by mass). It can be 0 to 4% by mass.
  • the oxide composite particles may not contain the other crystalline phase or the other amorphous phase.
  • the content of alumina in the oxide composite particles (the total mass of the oxide composite particles is 100% by mass) is preferably 15 to 50% by mass. When the content is 15% by mass or more, it is possible to secure a certain level of heat dissipation performance as a resin composition. Further, when the content is 50% by mass or less, it is possible to secure a low dielectric constant and a dielectric loss tangent that can be used even in a high frequency device.
  • the content can be, for example, 15 to 40% by mass, and can be 15 to 30% by mass.
  • the term "alumina” as used herein refers to all alumina components including components other than ⁇ -alumina. The alumina content is a value calculated from the amount charged at the time of synthesis.
  • the content of silica in the oxide composite particles (the total mass of the oxide composite particles is 100% by mass) is preferably 50 to 90% by mass. When the content is 50% by mass or more, it is possible to secure a low dielectric constant and dielectric loss tangent that can be used even in a high frequency device.
  • the silica content is a value calculated from the amount charged at the time of synthesis.
  • the oxide composite particles may contain other components other than silica and alumina, but may be made of silica and alumina.
  • the oxide composite particles have an element ratio of aluminum / silicon detected by XPS (X-ray Photoelectron Spectroscopy) of 1.5 or more. Since XPS can obtain information on elements existing on the surface of the measurement sample of several nm or less, the oxide composite particles according to the present embodiment having the element ratio of 1.5 or more are the surfaces of the oxide composite particles. It has a structure in which a large amount of alumina is present in the oxide composite particles and at least a part of the surface of the oxide composite particles is covered with an alumina layer.
  • the element ratio is preferably 2.0 or more, more preferably 2.3 or more. Since the surface of the oxide composite particles is preferably covered with an alumina layer as much as possible, it is preferable that the element ratio is high.
  • the elemental ratio of aluminum / silicon detected by XPS can be measured by a method described later.
  • the average particle size of the oxide composite particles is preferably 0.5 to 70 ⁇ m.
  • the average particle size is 0.5 ⁇ m or more, it is possible to secure a certain heat dissipation characteristic as a resin composition. Further, when the average particle size is 70 ⁇ m or less, it can be filled between materials as a heat dissipation filler for high frequency devices.
  • the average particle size can be, for example, 5 to 70 ⁇ m, 10 to 65 ⁇ m, and 20 to 60 ⁇ m.
  • the average particle size is measured using a laser diffraction type particle size distribution measuring device. Specifically, it can be measured by a method described later.
  • the average circularity of the oxide composite particles is preferably 0.7 or more. When the average circularity is 0.7 or more, a low viscosity of the resin composition can be achieved.
  • the average circularity is more preferably 0.8 or more, further preferably 0.85 or more, and particularly preferably 0.9 or more.
  • the upper limit of the range of the average circularity is not particularly limited, and a higher value is preferable for the average circularity, and it may be 1.
  • the average circularity is measured by the following method.
  • the oxide composite particles according to the present embodiment are required to have these physical characteristics (resin composition).
  • resin composition it is useful as a filler to be filled in a resin composition for a high frequency substrate).
  • the method for producing an oxide composite particle according to the present embodiment includes the following steps.
  • a mixture manufacturing step Also referred to as a mixture manufacturing step
  • a step of heating the mixture at 1300 to 1500 ° C. for 2 to 8 hours hereinafter, also referred to as a heating step.
  • the oxide composite particles according to the present embodiment can be easily and efficiently produced.
  • the silica particles used as a raw material are not particularly limited to crystalline systems such as amorphous, quartz and cristobalite, and the method for producing silica particles is not particularly limited, but SiO 2 containing an amorphous phase of 90% by mass or more is used. It is more preferable to use SiO 2 having an amorphous phase. Examples of the SiO 2 containing 90% by mass or more of the amorphous phase include SiO 2 manufactured by a flame melting method, an explosive combustion method, a gas phase method, a wet method, or the like.
  • the particle size of the oxide composite particles obtained after heating mainly reflects the particle size of the silica particles that are the raw materials. Therefore, the average particle size of the silica particles can be, for example, 0.5 to 70 ⁇ m, 3 to 65 ⁇ m, 20 to 60 ⁇ m, and 35 to 55 ⁇ m. The average particle size is measured in the same manner as the average particle size of the oxide composite particles. Further, since the shape of the oxide composite particles obtained after heating mainly reflects the shape of the silica particles as the raw material, the use of spherical silica particles can increase the average circularity of the oxide composite particles. It is preferable because it can be done.
  • the average circularity of the silica particles is preferably 0.60 or more, preferably 0.70 or more, and more preferably 0.80 or more. The average circularity is measured in the same manner as the average circularity of the oxide composite particles.
  • the alumina of the alumina particles used as a raw material is not particularly limited, and examples thereof include ⁇ -Al 2 O 3 , ⁇ -Al 2 O 3 , and ⁇ -Al 2 O 3 . These may be used alone or in combination of two or more.
  • the average value of the angle of repose of the alumina particles is preferably 50 ° or more, and more preferably 52 ° or more.
  • the average value of the rest angle is 50 ° or more, the fluidity of the alumina particles becomes low, and a sufficient amount of the alumina particles adheres to the surface of the silica particles at the time of mixing, so that the surface is sufficiently covered with the alumina layer.
  • Oxide composite particles having the same structure can be obtained.
  • the upper limit of the range of the average value of the angle of repose is not particularly limited, but may be, for example, 55 ° or less.
  • the average value of the angle of repose is a value measured by a method described later.
  • the average value of the angle of repose of Aerosil is less than 50 °, so that the alumina particles segregate on the surface of the silica particles and the surface is not sufficiently covered by the alumina layer. Therefore, the elemental ratio of aluminum / silicon detected by XPS is less than 1.5.
  • the specific surface area of the alumina particles is preferably 50 to 170 m 2 / g, more preferably 60 to 130 m 2 / g, and even more preferably 70 to 100 m 2 / g.
  • the specific surface area is 50 m 2 / g or more, the alumina particles are likely to be stably adsorbed on the silica surface, so that the degree of surface coating by the alumina layer is increased.
  • the specific surface area is 170 m 2 / g or less, the bulkiness of the alumina particles is suppressed to a certain level or less, and the oxide composite particles can be synthesized by the method.
  • the specific surface area is a value measured by a method described later.
  • the method of mixing the silica particles and the alumina particles may be either dry mixing or wet mixing, but since the dry mixing does not use a solvent, it is not necessary to dry the solvent and the production cost of the oxide composite particles can be reduced. Therefore, it is preferable.
  • the mixing method include agate mortar, a crusher such as a ball mill and a vibration mill, and various mixers.
  • Heating process In this step, the mixture obtained in the mixture manufacturing step is heated at 1300 to 1500 ° C. for 2 to 8 hours.
  • the heating device for heating the mixture is not particularly limited as long as it is a device capable of heating at a high temperature, and examples thereof include an electric furnace and a pusher furnace.
  • the heating atmosphere is not particularly limited, and examples thereof include the atmosphere, N2 , Ar, and under vacuum.
  • the heating temperature is preferably 1300 to 1500 ° C, more preferably 1300 to 1450 ° C, and even more preferably 1300 ° C to 1400 ° C.
  • the heating temperature is 1300 ° C. or higher, the content of cristobalite becomes large, and the thermal conductivity as a heat dissipation filler can be ensured.
  • the heating temperature is 1500 ° C. or lower, it is possible to prevent the circularity of the oxide composite particles from being lowered due to the fusion between the particles due to the heating.
  • the heating time is preferably 2 to 8 hours, more preferably 2 to 6 hours, still more preferably 4 to 5 hours.
  • the heating time is 2 hours or more, the content of cristobalite becomes large, and the thermal conductivity as a heat dissipation filler can be ensured. Further, when the heating time is 8 hours or less, it is possible to prevent the circularity of the oxide composite particles from being lowered due to the fusion between the particles due to the heating.
  • the oxide composite particles obtained after heating may be agglomerates in which a plurality of particles are aggregated.
  • the agglomerates themselves may be used as oxide composite particles, but if necessary, the agglomerates may be crushed and then used as oxide composite particles.
  • the method for crushing the agglomerates is not particularly limited, and examples thereof include a method for crushing with an agate mortar, a ball mill, a vibration mill, a jet mill, a wet jet mill, or the like.
  • the crushing may be carried out in a dry manner, or may be carried out in a wet manner by mixing with a liquid such as water or alcohol.
  • oxide composite particles are obtained by drying after crushing.
  • the drying method is not particularly limited, and examples thereof include heat drying, vacuum drying, freeze drying, and supercritical carbon dioxide drying.
  • the method for producing an oxide composite particle according to the present embodiment includes, for example, a classification step for classifying the oxide composite particle so as to obtain a desired average particle size, and an impurity reduction step, in addition to the mixture production step and the heating step. It may further include other steps such as a cleaning step for.
  • the resin composition according to the present embodiment contains the oxide composite particles according to the present embodiment and the resin. Since the resin composition according to the present embodiment contains the oxide composite particles according to the present embodiment, it can exhibit high thermal conductivity, low dielectric constant and dielectric loss tangent. Further, since the resin composition according to the present embodiment has a low viscosity, it has high fluidity and excellent moldability.
  • the resin is not particularly limited, and is, for example, polyamide such as polyethylene, polypropylene, epoxy resin, silicone resin, phenol resin, melamine resin, urea resin, unsaturated polyester, fluororesin, polyimide, polyamideimide, polyetherimide, and poly.
  • polyamide such as polyethylene, polypropylene, epoxy resin, silicone resin, phenol resin, melamine resin, urea resin, unsaturated polyester, fluororesin, polyimide, polyamideimide, polyetherimide, and poly.
  • Polyester such as butylene terephthalate and polyethylene terephthalate, polyphenylene sulfide, total aromatic polyester, polysulfone, liquid crystal polymer, polyethersulfone, polycarbonate, maleimide-modified resin, ABS resin, AAS (acrylonitrile-acrylic rubber / styrene) resin, AES (acrylonitrile) Ethylene / propylene / diene rubber-styrene) resin and the like can be mentioned. These resins may be used alone or in combination of two or more.
  • the content of the oxide composite particles in the resin composition is appropriately selected depending on the physical properties such as the target thermal conductivity, dielectric constant and dielectric loss tangent, but is preferably 20 to 80% by mass. This content is 11 to 67% by volume when the density of the oxide composite particles is 2.4 and the density of the resin is 1.2, and the density of the oxide composite particles is 3.1. When the density of the resin is 1.2, it is 9 to 61% by volume.
  • the resin composition according to the present embodiment can contain other components other than the oxide composite particles and the resin according to the present embodiment.
  • other components include flame retardants, glass cloth and the like.
  • the thermal conductivity, dielectric constant, dielectric loss tangent, and filling of the resin composition are further mixed. The rate and the like can be adjusted more easily.
  • the thermal conductivity of the resin composition according to the present embodiment is preferably 0.80 W / m ⁇ K or more, and more preferably 0.85 W / m ⁇ K or more.
  • the dielectric constant of the resin composition according to the present embodiment is preferably 4.0 or less, more preferably 3.5 or less.
  • the dielectric loss tangent of the resin composition according to the present embodiment is preferably 5.0 ⁇ 10 -4 or less, and more preferably 4.0 ⁇ 10 -4 or less.
  • the viscosity of the resin composition according to the present embodiment is preferably 700 Pa ⁇ s or less, and more preferably 500 Pa ⁇ s or less.
  • the thermal conductivity, dielectric constant, dielectric loss tangent and viscosity of the resin composition are values measured by a method described later.
  • the resin composition according to the present embodiment exhibits high thermal conductivity, low dielectric constant and dielectric loss tangent, and is therefore particularly useful as a resin composition for high-frequency substrates.
  • the high frequency substrate include a fluorine substrate, a PPE substrate, and a ceramic substrate.
  • Example 1 Silica particles (trade name: FB40R, manufactured by Denka Co., Ltd., average particle diameter: 50.1 ⁇ m) and alumina particles (trade name: AKPG07, manufactured by Sumitomo Chemical Co., Ltd., average rest angle: 52.5 °, specific surface area) Surface area: 80.0 m 2 / g) was added so that the amount of alumina particles added was 15% by mass. Further, the mixed particles were mixed with a vibration mixer (manufactured by Resodyn, trade name: low frequency resonance acoustic mixer Lab RAM II). 10 g of the obtained mixture was placed in an alumina crucible, heated from room temperature at 10 ° C./min, and heated in an electric furnace.
  • a vibration mixer manufactured by Resodyn, trade name: low frequency resonance acoustic mixer Lab RAM II
  • the heating temperature was 1400 ° C. and the heating time was 4 hours.
  • the sample was allowed to cool naturally, and after the sample was cooled, it was crushed in an agate mortar to obtain oxide composite particles.
  • the oxide composite particles were evaluated by the method described later.
  • Oxide composite particles were prepared and evaluated by the same method as in Example 1 except that the types and addition amounts of raw materials, heating time and heating temperature were changed to the conditions shown in Table 1 or Table 2.
  • silica particles (trade name: FB5D, manufactured by Denka Co., Ltd., average particle size: 8.0 ⁇ m) were used.
  • alumina particles (trade name: TM-DA, manufactured by Taimei Chemicals Co., Ltd., average angle of repose: 48.0 °, specific surface area: 6.6 m 2 / g) were used.
  • Alumina particles (trade name: FB40R, manufactured by Denka Co., Ltd., average particle diameter: 50.1 ⁇ m) or silica particles (trade name: FB5D, manufactured by Denka Co., Ltd., average particle diameter: 8.0 ⁇ m) and alumina particles (trade name: FB40R, manufactured by Denka Co., Ltd.).
  • the mixed particles were mixed with a vibration mixer (manufactured by Resodyn, trade name: low frequency resonance acoustic mixer Lab RAM II). 1 kg of the obtained mixture was placed in an alumina crucible, heated from room temperature at 2.5 ° C./min, and heated in an electric furnace. At this time, the heating temperature was 1400 ° C. and the heating time was 4 hours. After heating, the sample was allowed to cool naturally, and after the sample was cooled, it was crushed in an agate mortar to obtain oxide composite particles. The oxide composite particles were evaluated by the method described later.
  • the X-ray diffraction pattern of the oxide composite particles of Example 1 is shown in FIG.
  • Rietveld software manufactured by MDI, trade name: integrated powder X-ray software Jade + 9.6 was used for the quantitative analysis of the crystal phase.
  • the ratio (mass%) of various crystal phases was calculated by X-ray diffraction measurement of the oxide composite particle sample and Rietveld analysis.
  • each crystal phase determined by Rietveld analysis is C for ⁇ -cristobalite, A for ⁇ -alumina, M for mullite, and X for other crystal phases.
  • Rc, A ⁇ Rc / C, M ⁇ Rc / C and X ⁇ Rc / C which are obtained by multiplying C, A, M and X by the ratio Rc / C of C and the above-mentioned Rc, are the oxides, respectively.
  • the content (% by mass) of the ⁇ -cristobalite crystal phase, ⁇ -alumina crystal,glasse crystal and other crystal phases contained in the composite particles was defined, and the remaining components were determined to be amorphous.
  • the element ratio of aluminum / silicon on the surface of the oxide composite particle was measured using an X-ray photoelectron spectrometer (XPS, manufactured by Thermo, trade name: K-Alpha). After introducing the oxide composite particles into the apparatus, the measurement was performed by irradiating the measurement area of 400 ⁇ 200 ⁇ m with monochromatic Al—K ⁇ rays.
  • XPS X-ray photoelectron spectrometer
  • the average particle size was measured using a laser diffraction type particle size distribution measuring device (manufactured by Beckman Coulter, trade name: LS 13 320). 50 cm 3 of pure water and 0.1 g of a measurement sample were placed in a glass beaker, and a dispersion treatment was performed for 1 minute with an ultrasonic homogenizer (manufactured by BRANSON, trade name: SFX250). The dispersion liquid of the measurement sample subjected to the dispersion treatment was added drop by drop to the laser diffraction type particle size distribution measuring device with a dropper, and the measurement was performed 30 seconds after the predetermined amount was added.
  • a laser diffraction type particle size distribution measuring device manufactured by Beckman Coulter, trade name: LS 13 320. 50 cm 3 of pure water and 0.1 g of a measurement sample were placed in a glass beaker, and a dispersion treatment was performed for 1 minute with an ultrasonic homogenizer (manufactured by BRANSON, trade
  • the particle size distribution was calculated from the data of the light intensity distribution of the diffracted / scattered light by the measurement sample detected by the sensor in the laser diffraction type particle size distribution measuring device.
  • the average particle size was obtained by multiplying the measured particle size value by the relative particle amount (difference%) and dividing by the total relative particle amount (100%). In addition,% here is volume%.
  • the density of the oxide composite particles was measured by dry density measurement. An oxide composite particle sample that had been weighed in advance was placed in a measuring cell of a dry automatic densitometer (Curepic II 1340) manufactured by Shimadzu Corporation, and the volume and density of the sample were determined by dry measurement by filling with helium.
  • a dry automatic densitometer (Curepic II 1340) manufactured by Shimadzu Corporation
  • the average value of the angle of repose of the alumina particles was determined by measuring the angle of repose using a powder tester.
  • a powder tester PT-X manufactured by Hosokawa Micron, a dispersion sieve with an opening of 1700 ⁇ m is used, and the accumulation of alumina particles formed by supplying the sample while vibrating is photographed with a CCD camera and image processing is performed. The angle of repose was measured.
  • the specific surface area of the alumina particles was measured by gas adsorption measurement.
  • the measurement cell was filled with 1 g of a sample, and the specific surface area was measured by a fully automatic specific surface area system measuring device (BET one-point method) manufactured by Mt.
  • BET one-point method manufactured by Mt.
  • the degassing condition before the measurement was 200 ° C. for 10 minutes.
  • the adsorbed gas was nitrogen.
  • the thermal conductivity of the resin composition was calculated by multiplying the thermal diffusivity, specific gravity, and specific heat.
  • the thermal diffusivity was determined by processing the cured sample into a width of 10 mm ⁇ 10 mm ⁇ thickness of 1 mm and using a laser flash method.
  • a xenon flash analyzer (manufactured by NETZSCH, trade name: LFA447 NanoFlash) was used as the measuring device.
  • the specific density was determined using the Archimedes method.
  • the specific heat was determined by using a differential scanning calorimeter (manufactured by TA Instruments, trade name: Q2000) and raising the temperature from room temperature to 200 ° C. at a heating rate of 10 ° C./min under a nitrogen atmosphere.
  • Sheets were formed at °C for 5 minutes and 30,000 N to prepare an evaluation sample.
  • the thickness of the evaluation sample sheet is about 0.5 mm.
  • the shape and size do not affect the evaluation result if they can be mounted on the measuring instrument, but they are about 1 to 3 cm square.
  • the dielectric property was measured by the following method.
  • a 36 GHz hollow resonator manufactured by Samtec
  • a vector network analyzer (trade name: 85107, manufactured by KeySight Technology), and an evaluation sample (1.5 cm square, thickness 0.5 mm) was provided in the resonator.
  • a hole having a diameter of 10 mm was set to be closed, and the resonance frequency (f0) and the no-load Q value (Qu) were measured.
  • the evaluation sample was rotated for each measurement, and the measurement was repeated 5 times in the same manner, and the average of the obtained f0 and Qu was taken and used as the measured value.
  • the permittivity was calculated from f0, and the dielectric loss tangent (tan ⁇ c) was calculated from Qu using analysis software (software manufactured by Samtec).
  • the measured temperature was 20 ° C. and the humidity was 60% RH.
  • the oxide composite particles are mixed with a bisphenol A type liquid epoxy resin (manufactured by Mitsubishi Chemical Corporation, trade name: JER828) so that the filling amount of the oxide composite particles is 40% by volume of the whole, and a planetary stirrer (sinky) is used.
  • a resin composition was prepared by kneading with the company "Awatori Rentaro AR-250" (rotation speed 2000 rpm).
  • the viscosity of the obtained resin composition was measured under the following conditions using a leometer (“MCR-302” manufactured by Anton Pearl Co., Ltd.). Plate shape: Circular flat plate 10 mm ⁇ Sample thickness: 1 mm Temperature: 25 ⁇ 1 ° C Shear rate: 1s -1
  • the resin composition containing the oxide composite particles of Examples 1 to 8 according to the embodiment of the present invention has a high thermal conductivity (0.80 W / m ⁇ K or more). , Low dielectric constant (4.0 or less), and low dielectric loss tangent (5.0 ⁇ 10 -4 or less).

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EP21910102.9A EP4269343A4 (en) 2020-12-24 2021-11-24 COMPOSITE OXIDE PARTICLES, THEIR PRODUCTION METHOD, AND RESIN COMPOSITION
US18/269,481 US20240076470A1 (en) 2020-12-24 2021-11-24 Oxide composite particles, method for producing same and resin composition
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WO2025115797A1 (ja) * 2023-11-30 2025-06-05 デンカ株式会社 無機質粉末、および無機質粉末の製造方法
WO2025115794A1 (ja) * 2023-11-30 2025-06-05 デンカ株式会社 無機質粉末

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WO2025115794A1 (ja) * 2023-11-30 2025-06-05 デンカ株式会社 無機質粉末

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