Spherical calcium titanate powder, and resin composition
Patent Information
- Application Number
- PCT/JP2024/028004
- Authority / Receiving Office
- WO · WO
- Patent Type
- Applications
- Current Assignee / Owner
- Priority Date
- 2023-08-07
- Filing Date
- 2024-08-06
- Publication Date
- 2025-02-13
Smart Images

Figure JPOXMLDOC01-APPB-T000001
Abstract
Description
Spherical calcium titanate powder and resin composition
[0001] The present disclosure relates to a spherical calcium titanate powder and a resin composition.
[0002] In recent years, with the increase in the volume of information communication in the communications field, the use of high-frequency band signals has become widespread in electronic devices and communications devices. However, the application of high-frequency band signals to such devices has also raised the problem of increased transmission loss of circuit signals. Furthermore, as related electronic materials and components have become more highly functional, there has been a demand for further miniaturization of electronic devices and communications devices. Communication devices can be further miniaturized by increasing the dielectric constant of the antenna material incorporated therein. Therefore, there is a demand for materials (ceramic fillers) that can achieve a high dielectric constant and a low dielectric loss tangent.
[0003] By the way, perovskite complex oxides are mainly ABO, represented by barium titanate and strontium titanate. 3 This is a complex oxide represented by the formula: Powder of such perovskite complex oxides has a relatively high dielectric constant and is therefore expected to be a ceramic filler applicable to next-generation electronic devices. Of these, titanium-based complex oxides are used as electronic materials because they exhibit excellent electrical properties such as dielectricity, pyroelectricity, and piezoelectricity. Patent Document 1 describes a calcium titanate powder with high crystallinity and excellent electrical properties and a method for producing the same.
[0004] Since ceramic fillers are often used by filling them into resins, it is desirable for their shape to be as spherical as possible in order to improve their fillability and dispersibility in resins, thereby stabilizing their dielectric properties, and also in order to improve their processability and workability.The particles constituting the calcium titanate powder in Patent Document 1 have a square pillar or square pillar-like shape, and no powder containing spherical calcium titanate particles has been studied.
[0005] JP 2011-116645 A Japanese Patent No. 4155750 JP 2012-246203 A
[0006] An object of the present disclosure is to provide a spherical calcium titanate powder that has excellent fillability in resin and can achieve a higher relative dielectric constant and a low dielectric loss tangent, and a resin composition containing the spherical calcium titanate powder.
[0007] As a result of extensive investigation, the inventors of the present invention have found that the specific surface area (BET: m 2 They have found that a spherical calcium titanate powder having a ratio (D50 / BET) of the average particle diameter (D50:μm) to the average particle diameter (D50:μm / g) of 10 to 20 has excellent fillability into resin and can achieve a higher relative dielectric constant and a low dielectric dissipation factor. Furthermore, they have found that a resin composition containing the spherical calcium titanate powder and at least one resin selected from thermoplastic resins and thermosetting resins can be suitably used as a material that can achieve a high relative dielectric constant and a low dielectric dissipation factor.
[0008] According to the present disclosure, it is possible to provide a spherical calcium titanate powder that has excellent fillability in resin and can achieve a higher relative dielectric constant and a low dielectric loss tangent, and a resin composition containing the spherical calcium titanate powder.
[0009] An embodiment of the present disclosure will be described in detail below. However, the scope of the present disclosure is not limited to the embodiment described herein, and various modifications can be made without departing from the spirit of the present disclosure. Each aspect disclosed in this specification can be combined with any other feature disclosed in this specification. Furthermore, when multiple upper and lower limits are described for a particular parameter, any of these upper and lower limits can be combined to form a suitable numerical range. Furthermore, the lower and / or upper limits of a numerical range described in this disclosure are numerical values within that range and may be replaced with numerical values shown in the examples. The expression "X to Y" indicating a numerical range means "X or more and Y or less." If a specific description described for one embodiment also applies to other embodiments, that description may be omitted in other embodiments.
[0010] Each configuration and combination thereof in each embodiment is merely an example, and addition, omission, substitution, and other modifications of configurations are possible as appropriate within the scope of the gist of this disclosure. The present disclosure is not limited by the embodiments. Each aspect disclosed in this specification can be combined with any other feature disclosed in this specification. In this specification, "powder" means an aggregate of multiple particles.
[0011] [Spherical calcium titanate powder] The spherical calcium titanate powder according to this embodiment (hereinafter, sometimes simply referred to as "powder") has a specific surface area (BET: m 2 The ratio (D50 / BET) of the average particle diameter (D50:μm) to the average particle diameter (D50:μm) (D50 / BET) of the spherical calcium titanate powder according to this embodiment can achieve a higher relative dielectric constant. Furthermore, a low dielectric dissipation factor can also be achieved. In this disclosure, "spherical powder" means that when the powder is observed at 10,000x magnification using a scanning electron microscope, the shape of each particle is observed to be circular or rounded. Since the powder according to this embodiment is a calcium titanate powder containing spherical particles, it also has good fillability into resins.
[0012] The specific surface area (BET: m) of the spherical calcium titanate powder according to this embodiment 2 The ratio (D50 / BET) of the average particle diameter (D50: μm) to the specific surface area (μm / g) was calculated by measuring the average particle diameter (D50) (hereinafter sometimes referred to as "D50") and the specific surface area (BET) (hereinafter sometimes referred to as "BET") by the method described below, and then converting the value of D50 (μm) into the BET (m 2 / g) can be obtained.
[0013] <Average particle size (D50)> The average particle size (D50) (hereinafter sometimes referred to as "D50") of the spherical calcium titanate powder according to this embodiment can be measured under the following conditions. (Measuring conditions for average particle size) The average particle size is measured using a laser diffraction / scattering particle size distribution measuring device (for example, manufactured by Microtrackbell Co., Ltd., product name "MT3300EXII"). First, 80 cm 31 g of pure water and 0.1 g of spherical calcium titanate powder are added, and the mixture is dispersed for 1 minute using an ultrasonic homogenizer (for example, SMT Corporation, trade name "UH-600S" (homogenizer tip diameter: 20 mmφ)). The dispersed spherical calcium titanate powder dispersion is added drop by drop using a dropper to a laser diffraction / scattering particle size distribution analyzer. 30 seconds after the predetermined amount is added, the average particle size is measured. The particle size distribution is calculated from data on the light intensity distribution of diffracted / scattered light from the spherical calcium titanate powder detected by a sensor in the laser diffraction / scattering particle size distribution analyzer. D50 is calculated from the particle size corresponding to a cumulative value of 50% in the volume-based cumulative particle size distribution of the particle sizes measured. In this case, D50 (μm) is calculated by rounding the particle size to one decimal place.
[0014] <Specific Surface Area (BET)> The specific surface area of the spherical calcium titanate powder according to this embodiment can be measured by the BET multipoint method using a fully automatic specific surface area measuring device. Specifically, it can be measured under the following conditions. (Method for Measuring Specific Surface Area) The BET specific surface area of the spherical calcium titanate powder is measured by the following method. First, 4 g of spherical calcium titanate powder is filled into an empty cell, and degassed in an environment at 300°C. After the degassing process, the cell filled with the spherical calcium titanate powder is set in a fully automatic specific surface area measuring device (for example, Macsorb Model 1208, manufactured by Mountec Co., Ltd.), and the specific surface area is measured. The measurement gas is He—N 2 Using a mixed gas, measurements are taken using the multipoint method at a main flow rate of 25 mL / min.
[0015] The (D50 / BET) ratio of the spherical calcium titanate powder according to this embodiment is not particularly limited as long as it is in the range of 10 to 20. However, from the viewpoint of easily achieving a higher relative dielectric constant, a ratio of 10 to 19 is preferred. In one embodiment, from the viewpoint of easily obtaining a powder with a lower dielectric dissipation factor, (D50 / BET) may be 11 to 17, 12 to 19, 14 to 19, or 12 to 16. Note that "(D50 / BET) of 10 to 20" can be easily achieved, for example, by further heat-treating the spherical calcium titanate powder at a specific temperature to remove fine particles adhering to the particle surfaces and thereby lowering the BET. Furthermore, this can be more easily achieved by not performing a crushing treatment that would cause the D50 of the spherical calcium titanate powder after heat treatment to vary by 20% or more, or by recovering the powder without performing a crushing treatment, thereby suppressing a decrease in D50 and an increase in BET.
[0016] The D50 and BET ranges of the spherical calcium titanate powder can be adjusted as desired within the range where the aforementioned (D50 / BET) is 10 to 20. In one embodiment, from the viewpoint of easily obtaining a powder having a higher relative dielectric constant, the D50 of the spherical calcium titanate powder is preferably 0.5 to 15 μm. The D50 range may be 1 to 15 μm, 2 to 15 μm, 3 to 15 μm, 4 to 15 μm, 4 to 10 μm, 4 to 9 μm, 5 to 10 μm, 5 to 9 μm, or 6 to 9 μm. Furthermore, from the viewpoint of easily obtaining a powder having a higher relative dielectric constant, the BET of the powder is preferably 0.7 μm or less. 2 / g, preferably less than 0.5m 2 / g or less is more preferable, and 0.5m 2 More preferably, it is less than / g.
[0017] In the spherical calcium titanate powder according to this embodiment, the proportion of particles having a particle diameter of 0.2 times D50 is preferably equal to or less than a certain value. A low proportion of small particles having a particle diameter of 0.2 times D50 makes it easier to achieve a higher relative dielectric constant. In one embodiment, the proportion of particles having a particle diameter of 0.2 times D50 is preferably 1.5 vol% or less, more preferably 1.0 vol% or less, even more preferably 0.8 vol% or less, and particularly preferably 0.6 vol% or less. The proportion of particles having a particle diameter of 0.2 times D50 may be 0.5 vol% or less. In another embodiment, the proportion of particles having a particle diameter of 0.2 times D50 in the spherical calcium titanate powder may be 0 vol%. In this specification, "the proportion of particles is 0 vol%" means that, in measurement using the aforementioned laser diffraction / scattering particle size distribution analyzer, the cumulative value of a specific particle is 0, or the particle is not detected (below the lower measurement limit). The proportion of particles having a particle diameter 0.2 times D50 can be determined by the following steps: 1. Measure D50 according to the "Measurement conditions for average particle diameter" described above. 2. Multiply D50 by 0.2 to calculate the particle diameter. At this time, round off to one decimal place to calculate the particle diameter to one decimal place. 3. The proportion of particles having a particle diameter 0.2 times D50 obtained in 2 (the particle diameter to one decimal place obtained by rounding off to one decimal place the particle diameter calculated by multiplying D50 by 0.2 described above) is determined from the volume-based cumulative particle size distribution.
[0018] When the D50 of the powder according to this embodiment is 0.5 to 15 μm, the particle diameter 0.2 times D50 is 0.1 to 3.0 μm. If the proportion of particles having such a particle diameter is 1.5 vol% or less, it becomes easier to control (D50 / BET) within the range of 10 to 20, and it becomes easier to obtain a powder with a higher relative dielectric constant. Note that the particle diameter 0.2 times D50 may be in the range of 1.0 to 1.8 μm.
[0019] When the powder according to this embodiment has a D50 of 4 μm or more, more preferably in the range of 4 to 15 μm, it is preferable that the proportion of particles having a particle diameter of 2.0 μm or less be a certain value or less. That is, when the D50 of the powder is 4 μm or more, if the proportion of particles having a particle diameter of 2.0 μm or less is a certain value or less, preferably 4.0 vol% or less, it is easy to control (D50 / BET) within the range of 10 to 20. As a result, it is easy to obtain a powder having a higher relative dielectric constant. Note that, from the viewpoint of easily controlling (D50 / BET) within the range of 10 to 20, the proportion of particles having a particle diameter of 2.0 μm or less is preferably 3.0 vol% or less, more preferably 2.5 vol% or less, even more preferably 2.0 vol% or less, and particularly preferably 1.5 vol% or less. Furthermore, the proportion of the particles may be 1.0 vol% or less.
[0020] Similarly, when the D50 of the powder is 4 μm or more, from the viewpoint of easily controlling (D50 / BET) within the range of 10 to 20, it is preferable that the proportion of particles having a particle diameter of 1.0 μm or less is also a certain value or less. In one embodiment, the proportion of particles having a particle diameter of 1.0 μm or less may be 1.0 vol% or less, or may be 0.5 vol% or less. Furthermore, the proportion of particles having a particle diameter of 1.0 μm or less in the spherical calcium titanate powder may be 0 vol%. The proportion of particles having a particle diameter of 2.0 μm or less and the proportion of particles having a particle diameter of 1.0 μm or less can be calculated from the cumulative value of particles having a particle diameter of 2.0 μm or less or the cumulative value of particles having a particle diameter of 1.0 μm or less, based on the volume-based particle size distribution measured according to the above-mentioned average particle diameter measurement conditions.
[0021] <Average Sphericity> The spherical calcium titanate according to this embodiment preferably has an average sphericity of 0.80 or more. An average sphericity of 0.80 or more facilitates improved fillability and dispersibility in resin. The average sphericity of the spherical calcium titanate powder may be 0.85 or more, 0.86 or more, or even 0.87 or more. In one embodiment, the average sphericity of the powder may be in the range of 0.84 or more and less than 0.90. The average sphericity of the spherical calcium titanate powder can be measured by the following method. (Method for Measuring Average Sphericity) Measurement is performed using a powder image analyzer (e.g., Spectris, product name "FPIA-3000") according to the following procedure. A measurement sample is obtained by dispersing a sample in pure water. The measurement sample is then passed through a planar extensional flow cell of the device, and 200 or more spherical calcium titanate particles moving within the cell are recorded as images using an objective lens. The average sphericity is calculated from this recorded image and the following formula (1): Average sphericity = (π×HD / PM) 2 ... (1) In formula (1), HD represents the equivalent circle diameter of the particle and is calculated from the area ratio of the projected area of the target particle to the area of a perfect circle. PM represents the projected perimeter of the target particle. The average sphericity can be calculated by first calculating the "average circularity" from the average value of the circularities (π × HD / PM) of 200 spherical calcium titanate particles, and then squaring this average circularity.
[0022] The calcium titanate constituting the spherical calcium titanate powder according to this embodiment is represented by the general formula ABO 3 It is a composite oxide having a perovskite-type crystal structure represented by the formula: CaTiO 3 The crystal structure of the spherical calcium titanate powder can be determined by X-ray diffraction measurement.
[0023] In one embodiment, the spherical calcium titanate powder may be surface-treated with a surface treatment agent. Surface treatment with a surface treatment agent tends to improve the fillability of the spherical calcium titanate powder in resin. Examples of surface treatment agents include silane coupling agents and aluminate coupling agents. These may be used alone or in combination of two or more. Among these, treatment with a silane coupling agent is preferred from the viewpoint of easily reducing polar functional groups on the particle surface, and silazanes such as hexamethyldisilazane (HMDS) and silane coupling agents having a vinyl group such as vinyltrimethoxysilane are more preferred.
[0024] In one embodiment, by treating the spherical calcium titanate powder with a surface treatment agent having a hydrophobic functional group, such as vinylsilane or hexamethyldisilazane (HMDS), the polar functional groups on the particle surfaces constituting the powder are easily reduced, making it easier to achieve a lower dielectric tangent. Whether the spherical calcium titanate powder has been surface-treated or not can be confirmed by analyzing the powder using, for example, IR, TG-DTA, mass spectrometry, or the like.
[0025] The spherical calcium titanate powder according to this embodiment may contain other components in addition to calcium titanate. Examples of such other components include calcium carbonate and titanium oxide. These other components may be contained alone or in combination of two or more. When the spherical calcium titanate powder according to this embodiment contains other components, the amount of such other components is preferably 1% by mass or less, and more preferably 0.5% by mass or less, relative to the total mass of the spherical calcium titanate powder. From the viewpoint of reducing the dielectric loss tangent, it is preferable that the spherical calcium titanate powder does not contain other components.
[0026] In one embodiment, the relative dielectric constant at 1 GHz of the spherical calcium titanate powder according to this embodiment, measured under the conditions described below, is preferably 50 or more, more preferably 60 or more. The relative dielectric constant may be 70 or more, or may be 85 or more. Similarly, the dielectric loss tangent at 1 GHz, measured under the conditions described below, is 4.5×10 -3Preferably, the value is 3.0 x 10 or less. -3 The following is more preferred:
[0027] As described above, the spherical calcium titanate powder according to this embodiment can achieve a higher dielectric constant and a lower dielectric dissipation factor than conventional powders, and can therefore be used, for example, as a ceramic filler for devices operating in the 10 to 60 GHz band. Typical calcium titanate powders have a high dielectric constant but also a high dielectric dissipation factor, as shown in Reference Example 1 below. Furthermore, such calcium titanate powders have poor fillability and dispersibility in resins. The present inventors attempted to improve the dielectric properties by spheroidizing calcium titanate powder to improve its dispersibility and fillability in resins. They then found that by adjusting the crystallinity and reducing the interaction between the resin and the powder interface, a low dielectric dissipation factor can be achieved while maintaining a high level of dielectric constant.
[0028] Furthermore, the present inventors have investigated how to further increase the dielectric constant of spherical calcium titanate powder and have surprisingly found that by controlling the ratio of D50 to specific surface area (D50 / BET) of the spherical calcium titanate powder within a certain range, it is possible to achieve a higher dielectric constant than conventional ones and at the same time a low dielectric dissipation factor.The powder according to this embodiment has a slightly higher D50 value relative to BET, which indicates that the particles are somewhat coherent, which is presumably why it improves crystallinity and makes it easier to achieve a sintered, dense form, thereby enabling the development of a high dielectric constant.
[0029] [Method for producing spherical calcium titanate powder] The spherical calcium titanate powder according to this embodiment may be produced, for example, by a method comprising spheronizing a raw material calcium titanate powder (step (i)) and heating the spherical calcium titanate powder at 600 to 1200° C. (step (ii)). Hereinafter, one embodiment of the method for producing spherical calcium titanate powder comprising steps (i) and (ii) will be described.
[0030] <Step (i)> In the production method according to this embodiment, step (i) is a step of spheronizing the raw material calcium titanate powder. By including step (i), it becomes easier to obtain a powder that has excellent fillability into resin. In step (i), the raw material calcium titanate powder is preferably spheronized by a powder fusion method. The raw material calcium titanate powder (hereinafter simply referred to as "raw material powder") preferably has an average particle size (D50) of 0.2 to 30 μm, more preferably 1 to 20 μm, from the viewpoints of the average particle size of the powder after spheronization, ease of handling of the powder, and ease of feeding. Furthermore, the average sphericity of the raw material powder is not particularly limited.
[0031] The method for preparing the raw material powder is not particularly limited. For example, titanium oxide (TiO 2 ) and calcium carbonate (CaCO 3 The raw material powder may be a bulk powder of calcium titanate obtained by reacting a calcium titanate powder with a calcium stearate powder under high temperature conditions, or a calcium titanate powder prepared by a wet method. From the viewpoints of availability and economy, it is preferable to use a calcium titanate powder prepared by a solid-phase method.
[0032] The raw material powder contains impurities such as alkali metal elements such as Li, Na, and K, and metal elements such as Fe, and Cl, from the viewpoint of reducing the dielectric loss tangent and the reliability of the electronic material. - ,Br - It is preferable that the content of anions such as these is low. Specifically, it is preferable that the total amount of these impurities and anions in the raw material powder is 0.01 mass % or less.
[0033] As described above, step (i) is preferably a step of spheroidizing the raw material powder by a powder melting method. The powder melting method is a method of spheroidizing the raw material powder by introducing it into a high-temperature condition above the melting point, for example, a flame, plasma, electric furnace, gas furnace, etc., and for example, methods such as those described in Patent Documents 2 and 3 can be used. The melting atmosphere is not particularly limited, but from the viewpoint of easily preventing reduction of the raw material powder, it is desirable to spheroidize it in an environment with a high oxygen partial pressure, for example, LPG / O 2The raw material powder can be spheroidized in a flame using a gas. The method of adding the raw material powder is not particularly limited, and the raw material powder may be supplied as a dry powder or as a slurry in which the powder is dispersed in water, alcohol, or the like.
[0034] In one embodiment, step (i) may involve spheroidizing the raw material powder to prepare a spherical calcium titanate powder having an average sphericity of 0.80 or more.
[0035] <Step (ii)> The production method according to this embodiment includes, after step (i), heating the spheroidized calcium titanate powder at 600 to 1200°C (step (ii)). By further heating at 600 to 1200°C after step (i), fine particles on the surfaces of the calcium titanate particles are easily removed, and the BET of the resulting powder is likely to decrease. As a result, it is easy to control (D50 / BET) within the range of 10 to 20.
[0036] The heating temperature in step (ii) is preferably 600 to 1150°C, more preferably 600 to 1100°C, even more preferably 800 to 1000°C, and particularly preferably above 800°C and up to 1000°C. Heat-treating the spheroidized calcium titanate powder at such a heating temperature makes it possible to adjust the crystallinity and reduce the amount of impurities. It also facilitates the removal of fine particles adhering to the surfaces of the calcium titanate particles. As a result, the specific surface area of the particles is reduced, making it easier to control (D50 / BET) to 10 to 20, and thus facilitating the achievement of a high dielectric constant and a low dielectric loss tangent while ensuring high reliability.
[0037] As the heating device, for example, an electric furnace or a gas furnace can be used. Step (ii) is preferably carried out in the atmosphere. The heating time is preferably 1 to 24 hours, more preferably 1 to 12 hours. If the heating time is 1 to 24 hours, productivity tends to be good.
[0038] In one embodiment, after step (ii), it is preferable not to carry out a crushing treatment that would cause the average particle size (D50) of the obtained spherical calcium titanate powder to vary by 20% or more.Furthermore, from the viewpoint of facilitating the production of spherical calcium titanate powder having a higher dielectric constant, it is preferable to recover the powder after step (ii) without carrying out a crushing treatment.
[0039] By carrying out step (ii), calcium titanate particles may coalesce to form aggregates. In the production method according to this embodiment, it is preferable not to carry out a treatment for finely breaking down the aggregates, for example, a crushing treatment that would cause the average particle size (D50) of the spherical calcium titanate powder to vary by 20% or more.
[0040] Examples of crushing treatments that result in a 20% or greater change in the D50 of spherical calcium titanate powder include crushing the powder for 30 minutes or longer using an agate mortar, ball mill, vibration mill, jet mill, wet jet mill, etc. In the production method according to this embodiment, by not performing the crushing treatment for 30 minutes or longer, or by not performing the crushing treatment at all, the spherical calcium titanate powder is crushed, the proportion of small particles increases, and the BET value is easily prevented from increasing. As a result, it is easier to control the (D50 / BET) value of the final spherical calcium titanate powder, making it easier to obtain a powder that has a higher dielectric constant and a low dielectric loss tangent. When the crushing treatment is performed, the crushing time is preferably 20 minutes or less.
[0041] The production method according to this embodiment may also include a step of classifying the spherical calcium titanate powder to obtain a spherical calcium titanate powder having a desired average particle size (D50). Examples of classification methods include sieving, liquid cyclone classification, and air classification. Furthermore, the method may also include a step of surface-treating the spherical calcium titanate powder with a surface treatment agent, a washing step to reduce impurities (e.g., the aforementioned anions) in the spherical calcium titanate powder, and the like.
[0042] In one embodiment, the spherical calcium titanate powder according to this embodiment may be blended or mixed with other spherical calcium titanate powders having different specific surface areas or average particle diameters (D50), or other inorganic metal powders, or inorganic oxide powders, to form a mixed powder. By forming a mixed powder, the relative permittivity, dielectric loss tangent, thermal expansion coefficient, thermal conductivity, packing ratio, etc., when blended with a resin material can be easily adjusted to desired ranges. When forming a mixed powder, other powders are blended in such a range that the mixed powder's (D50 / BET) ratio is in the range of 10 to 20.
[0043] [Uses] The spherical calcium titanate powder according to this embodiment can simultaneously achieve a higher dielectric constant and a low dielectric loss tangent when filled into a resin, and can therefore be suitably used as a powder for filling resins (a filler for resins, particularly a ceramic filler for sealing materials used in high-frequency bands).
[0044] [Resin Composition] The resin composition according to this embodiment contains the spherical calcium titanate powder described above and at least one resin selected from thermoplastic resins and thermosetting resins. The content of the spherical calcium titanate powder in the resin composition is not particularly limited and can be adjusted appropriately depending on the purpose. The spherical calcium titanate powder according to this embodiment does not deteriorate in processability or workability even when highly loaded in a resin, so the amount of powder blended in the resin composition can be adjusted to obtain the desired dielectric properties. For example, when used as a substrate material for high-frequency bands or as an insulating material, the powder may be blended in an amount ranging from 1 to 80% by mass, more preferably from 10 to 70% by mass, based on the total mass of the resin composition.
[0045] <Resin> The resin composition according to this embodiment contains at least one resin selected from thermoplastic resins and thermosetting resins. More specifically, examples of the resin include polyethylene resins; polypropylene resins; epoxy resins; silicone resins; phenolic resins; melamine resins; urea resins; unsaturated polyester resins; fluororesins; polyamide-based resins such as polyimide resins, polyamideimide resins, and polyetherimide resins; polyester-based resins such as polybutylene terephthalate resins and polyethylene terephthalate resins; polyphenylene sulfide resins; wholly aromatic polyester resins; polysulfone resins; liquid crystal polymer resins; polyethersulfone resins; polycarbonate resins; maleimide-modified resins; ABS resins; AAS (acrylonitrile-acrylic rubber-styrene) resins; AES (acrylonitrile-ethylene-propylene-diene rubber-styrene) resins; hydrocarbon-based elastomer resins; polyphenylene ether resins; and aromatic polyene-based resins. These may be used alone or in combination of two or more.
[0046] The resin composition according to this embodiment may contain a curing agent, a curing accelerator, a release agent, a coupling agent, a colorant, a flame retardant, an ion scavenger, etc., within the range that does not impair the effects of the present invention.
[0047] <Method for Producing Resin Composition> The method for producing the resin composition is not particularly limited, and the resin composition can be produced by stirring, dissolving, mixing, and dispersing predetermined amounts of each material. The apparatus for mixing, stirring, dispersing, etc., of these mixtures is not particularly limited, and examples that can be used include a mortar and pestle machine equipped with a stirring and heating device, a three-roll mill, a ball mill, a planetary mixer, etc. These apparatuses may also be used in appropriate combination.
[0048] As described above, the resin composition containing the spherical calcium titanate powder according to this embodiment can achieve a high relative dielectric constant and a low dielectric loss tangent.
[0049] The present invention will be described in detail below with reference to examples, but the present invention is not limited to the following description.
[0050] Example 1 The raw material powder described in Reference Example 1 (calcium titanate powder; manufactured by Kyoritsu Material Co., Ltd., product name "CT-3", average sphericity of aggregates: 0.78, average particle diameter (D50): 3.1 μm, specific surface area (BET): 1.82 m 2 / g) to LPG / O 2 The particles were spheroidized by a powder fusion method in a gas flame and then heat-treated at 1000°C for 6 hours. The particles were then collected without being crushed to obtain the spherical calcium titanate powder of Example 1. The average particle size (D50), the proportion of particles having each particle size, the specific surface area (BET), and the average sphericity of the obtained spherical calcium titanate powder were measured under the following conditions. The results are shown in Table 1.
[0051] (Measuring conditions for average particle size) The average particle size was measured using a laser diffraction / scattering particle size distribution measuring device (manufactured by Microtrackbell Co., Ltd., product name "MT3300EXII"). First, 80 cm 3 1 g of pure water and 0.1 g of spherical calcium titanate powder were added and dispersed for 1 minute using an ultrasonic homogenizer (manufactured by SMT Corporation, product name "UH-600S" (homogenizer tip diameter: 20 mmφ)). The dispersed spherical calcium titanate powder dispersion was added dropwise using a dropper to a laser diffraction / scattering particle size distribution analyzer. 30 seconds after the addition of the predetermined amount, the average particle size was measured. The particle size distribution was calculated from the light intensity distribution data of the diffracted / scattered light of the spherical calcium titanate powder detected by the sensor in the laser diffraction / scattering particle size distribution analyzer. D50 was calculated from the particle size corresponding to the cumulative value of 50% in the volume-based cumulative particle size distribution of the measured particle size. Furthermore, the proportion of particles having a particle size 0.2 times the D50 was calculated according to steps 1 to 3 above. For powders with a D50 of 4 μm or more, the proportion of particles with a particle size of 2.0 μm or less and the proportion of particles with a particle size of 1.0 μm or less were calculated from the obtained cumulative particle size distribution.
[0052] (Method for measuring specific surface area) The BET specific surface area of the spherical calcium titanate powder was measured by the following method. First, 4 g of powder was filled into an empty cell, and degassing treatment was performed in an environment of 300°C. After degassing treatment, the cell filled with the spherical calcium titanate powder was set in a fully automatic specific surface area measuring device (manufactured by Mountec Co., Ltd., product name "Macsorb Model 1208"), and the specific surface area was measured. The measurement gas was He—N 2 Measurements were carried out by the multipoint method using a mixed gas at a main flow rate of 25 mL / min.
[0053] (Method for measuring average sphericity) Measurement was carried out using a powder image analyzer (manufactured by Spectris, product name "FPIA-3000") according to the following procedure. A sample was dispersed in pure water to obtain a measurement sample. The measurement sample was flowed into a planar extensional flow cell of the device, and 200 or more spherical calcium titanate particles moving within the cell were recorded as images using an objective lens. The average sphericity was calculated from this recorded image and the following formula (1): Average sphericity = (π × HD / PM) 2 ... (1) In formula (1), HD represents the equivalent circle diameter of the particle, and is calculated from the area ratio of the projected area of the target particle to the area of a perfect circle. PM represents the projected perimeter of the target particle. The average sphericity was calculated by first calculating the "average circularity" from the average value of the circularity (π × HD / PM) of 200 spherical calcium titanate particles, and then squaring the average circularity.
[0054] Next, the dielectric constant and dielectric loss tangent of the resin composition containing the spherical calcium titanate powder were measured under the following conditions to determine the filler-equivalent dielectric constant and dielectric loss tangent. (Evaluation of Dielectric Properties (Dielectric Constant and Dielectric Loss Tangent)) The dielectric properties of the spherical calcium titanate powder were measured using a powder dielectric constant measuring instrument (manufactured by Keycom Corporation, product name "TM Cavity Resonator" (cylindrical cavity resonance method)). A PTFE resin cell (cylindrical, volume 1154 cm) was used. 3 ) was filled with 2.5 to 3.0 g of spherical calcium titanate powder and set in the apparatus, and then the resonance peak at 1 GHz was read to measure the relative permittivity and dielectric loss tangent.
[0055] [Examples 2 to 4] Spherical calcium titanate powders were obtained under the production conditions shown in Table 1. For each spherical calcium titanate powder, the average particle size (D50), the proportion of particles having each particle size, the specific surface area (BET), and the average sphericity were measured using the same methods as in Example 1. The dielectric properties of the powders were also evaluated under the same conditions as in Example 1. The results are shown in Table 1.
[0056] [Examples 5 to 8] The spherical calcium titanate powder obtained in Example 1 was crushed in an agate mortar under the conditions shown in Table 1 to obtain spherical calcium titanate powder. For each spherical calcium titanate powder, the average particle size (D50), the proportion of particles having each particle size, the specific surface area (BET), and the average sphericity were measured in the same manner as in Example 1. The dielectric properties of the powder were also evaluated under the same conditions as in Example 1. The results are shown in Table 1.
[0057] Comparative Examples 1 to 5: The raw material powder was spheronized under the conditions shown in Table 1. Then, drying treatment was carried out at 100°C for 1 hour to obtain spherical calcium titanate powder for each example. For the spherical calcium titanate powder for each example, the average particle size (D50), the proportion of particles having each particle size, specific surface area (BET), and average sphericity were measured in the same manner as in Example 1. The dielectric properties of the powder were also evaluated under the same conditions as in Example 1. The results are shown in Table 1.
[0058]
[0059] As shown in Table 1, the spherical calcium titanate powders of Examples 1 to 8, which satisfy the configuration of this embodiment, had a higher dielectric constant than the spherical calcium titanate powders of Comparative Examples 1 to 5. Furthermore, a comparison of Example 1 with Examples 5 to 8 revealed that a higher dielectric constant and lower dielectric dissipation factor could be achieved without the crushing treatment. Furthermore, the spherical calcium titanate powders of Examples 1 to 8 also had a high average sphericity and good resin fillability. These results confirm that the spherical calcium titanate powder according to this embodiment has excellent resin fillability and can achieve a higher dielectric constant and low dielectric dissipation factor.
[0060] A non-limiting list of exemplary embodiments and combinations of exemplary embodiments of the present disclosure is set forth below: [1] Specific surface area (BET: m2 [2] A spherical calcium titanate powder according to [1], having an average sphericity of 0.80 or more. [3] The specific surface area (BET) of the spherical calcium titanate powder is 0.5 m or less. 2 / g or less. [4] The spherical calcium titanate powder according to any one of [1] to [3], wherein the average particle diameter (D50) is 0.5 to 15 μm. [5] The spherical calcium titanate powder according to any one of [1] to [4], which is for use as a resin filler. [6] A resin composition comprising the spherical calcium titanate powder according to any one of [1] to [5], and at least one resin selected from a thermoplastic resin and a thermosetting resin.
[0061] The spherical calcium titanate powder according to this embodiment can simultaneously achieve a higher dielectric constant and a lower dielectric loss tangent when filled into a resin, and therefore has industrial applicability as a powder for filling resins (a filler for resins, particularly a ceramic filler for sealing materials in high-frequency bands).
Claims
1. Specific surface area (BET: m 2 The ratio (D50 / BET) of the average particle diameter (D50:μm) to the average particle diameter (D50:μm) (D50 / g) is 10 to 20.
2. The spherical calcium titanate powder according to claim 1, having an average sphericity of 0.80 or more.
3. The specific surface area (BET) is 0.5 m 2 3. The spherical calcium titanate powder according to claim 1 or 2, wherein the average molecular weight of the powder is 1 / g or less.
4. The spherical calcium titanate powder according to claim 1 or 2, wherein the average particle size (D50) is 0.5 to 15 μm.
5. The spherical calcium titanate powder according to claim 1 or 2, which is for use in filling with resin.
6. A resin composition comprising the spherical calcium titanate powder according to claim 1 or 2 and at least one resin selected from thermoplastic resins and thermosetting resins.
Citation Information
Patent Citations
Production of powder of perovskite type compound oxide
JP1993009023A
Production of powder of perovskite type compound oxide
JP1993009025A
Calcium titanate powder
JP2023098213A
Barium titanate-based powder, and production method therefore and use thereof
WO2017171038A1
Barium titanate powder, production method therefor, and filler for sealing material
WO2022202133A1
