THERMALLY CONDUCTIVE PARTICLE-FILLED FIBER
20200239759 ยท 2020-07-30
Inventors
- Kazuhide YOSHIYAMA (Shibukawa-shi, Gunma, JP)
- Kensuke NAKA (Kyoto-shi, Kyoto, JP)
- Kimihiro MATSUKAWA (Kyoto-shi, Kyoto, JP)
Cpc classification
C08K2201/003
CHEMISTRY; METALLURGY
C08L33/14
CHEMISTRY; METALLURGY
C08J2433/14
CHEMISTRY; METALLURGY
D01D5/0038
TEXTILES; PAPER
C08L2205/025
CHEMISTRY; METALLURGY
C08L33/14
CHEMISTRY; METALLURGY
D01F1/09
TEXTILES; PAPER
C08L2201/10
CHEMISTRY; METALLURGY
D01D5/003
TEXTILES; PAPER
C08K2003/282
CHEMISTRY; METALLURGY
D01F6/00
TEXTILES; PAPER
C08L63/00
CHEMISTRY; METALLURGY
C08L101/00
CHEMISTRY; METALLURGY
D10B2321/08
TEXTILES; PAPER
C08J5/04
CHEMISTRY; METALLURGY
D01F6/44
TEXTILES; PAPER
C08J2333/14
CHEMISTRY; METALLURGY
International classification
C08L33/14
CHEMISTRY; METALLURGY
Abstract
The present invention is a thermally conductive particle-filled fiber containing a resin and thermally conductive particles, wherein at least some of the thermally conductive particles are present inside the fiber, an average particle diameter of the thermally conductive particles is 10 to 1000 nm, and an average fiber diameter of the fiber is 50 to 10000 nm.
Claims
1.-7. (canceled)
8. A resin composition comprising: a thermally conductive particle-filled fiber having an average fiber diameter of 50 to 10000 nm and comprising a resin and thermally conductive particles having an average particle diameter of 10 to 1000 nm; and a resin, hereinafter referred to as a matrix resin, wherein the matrix resin comprises thermally conductive particles.
9. The resin composition according to claim 8, wherein the thermally conductive particles in the matrix resin are one or more selected from metal oxide particles, metal nitride particles and carbon particles.
10. The resin composition according to claim 8, wherein the thermally conductive particles in the matrix resin are one or more selected from aluminum oxide particles, magnesium oxide particles and crystalline silica particles.
11. The resin composition according to claim 8, having a transmittance of not less than 80% T.
12. The resin composition according to claim 8, wherein the resin of the thermally conductive particle-filled fiber is one or more resins selected from epoxy resins, acrylic resins, amide-imide resins, phenolic resins, silicone resins and the like.
13. The resin composition according to claim 8, wherein the thermally conductive particle-filled fiber comprises 20 to 90 mass % of the thermally conductive particles.
14. The resin composition according to claim 8, wherein the thermally conductive particle-filled fiber has an average fiber length of 100 m or more.
15. The resin composition according to claim 8, wherein the thermally conductive particles of the thermally conductive particle-filled fiber are one or more selected from metal oxide particles, metal nitride particles and carbon particles.
16. The resin composition according to claim 8, wherein the thermally conductive particles of the thermally conductive particle-filled fiber are one or more selected from magnesium oxide particles, aluminum oxide particles, boron nitride particles, aluminum nitride particles, silicon nitride particles, nanodiamonds, carbon nanotubes and graphene particles.
17. A process for producing the resin composition according to claim 8, the process having: step (I) of producing a thermally conductive particle-filled fiber having an average fiber particle of 50 to 10000 nm and comprising a resin and thermally conductive particles having an average particle diameter of 10 to 1000 nm; and step (II) of blending the thermally conductive particle-filled fiber obtained in step (I) and thermally conductive particles with a resin, wherein step (I) has a step of spinning by an electrospinning method using a polymer solution comprising the resin, the thermally conductive particles and a solvent.
18. A process for producing the resin composition according to claim 17, wherein in step (II), the thermally conductive particle-filled fiber and the thermally conductive particles are blended with the resin by mixing the thermally conductive particle-filled fiber and the thermally conductive particles with a constituent monomer of the resin and polymerizing the constituent monomer.
19. A thin film composed of the resin composition according to claim 8.
20. The thin film according to claim 19, having a transmittance of not less than 80% T.
Description
BRIEF DESCRIPTION OF DRAWING
[0023]
EMBODIMENTS OF THE INVENTION
Thermally Conductive Particle-Filled Fiber and Production Process for the Same
[0024] The present invention relates to a fine fiber having an average fiber diameter of 50 to 10000 nm and containing a resin and thermally conductive particles having an average particle diameter of 10 to 1000 nm. The fiber of the present invention is a resin fiber having an average fiber diameter of 50 to 10000 nm and composed of a resin in which thermally conductive particles having an average particle diameter of 10 to 1000 nm are dispersed.
[0025] The thermally conductive particle-filled fiber of the present invention contains a resin and thermally conductive particles.
[0026] The resin is one or more resins selected from epoxy resins, acrylic resins, amide-imide resins, phenolic resins, silicone resins, and the like. The resin may be a resin having a curable group such as an epoxy group.
[0027] The thermally conductive particle-filled fiber of the present invention preferably contains 25 to 90 mass %, more preferably 25 to 80 mass %, further preferably 50 to 70 mass %, of the resin.
[0028] In the present invention, the thermally conductive particle refers to a particle having a thermal conductivity of not less than 1.0 W/m.Math.K.
[0029] The average particle diameter of the thermally conductive particles is 10 to 1000 nm, preferably 10 to 500 nm, more preferably 10 to 100 nm. The thermally conductive particles having such an average particle diameter, e.g., magnesium oxide particles, can be obtained by, for example, a gas phase oxidation method.
[0030] Here, the average particle diameter of the thermally conductive particles is one measured by dynamic light scattering measurement (DLS). The average particle diameter can be measured by, for example, a dynamic light scattering photometer, and specifically, the average particle diameter can be measured by stirring the thermally conductive particles in a dispersion medium with a magnetic stirrer for about 24 hours to disperse them and subjecting the resulting dispersion to measurement using a dynamic light scattering photometer (e.g., model number: DLS-7000HL manufactured by Otsuka Electronics Co., Ltd.).
[0031] As the thermally conductive particles, one or more selected from metal oxide particles, metal nitride particles and carbon particles can be mentioned. As the thermally conductive particles, specifically, one or more selected from magnesium oxide particles, aluminum oxide particles, boron nitride particles, aluminum nitride particles, silicon nitride particles, nanodiamonds, carbon nanotubes and graphene particles can be mentioned. Preferred are metal oxide particles, and more preferred are magnesium oxide particles.
[0032] The thermally conductive particle-filled fiber of the present invention preferably contains 20 to 90 mass %, more preferably 25 to 90 mass %, further preferably 30 to 90 mass %, furthermore preferably 30 to 80 mass %, furthermore preferably 30 to 60 mass %, of the thermally conductive particles. Regarding the resin composition of the present invention described later, when the same amount of thermally conductive particles are blended in the resin composition, it is sometimes advantageous to use the thermally conductive particle-filled fiber of the present intention containing the thermally conductive particles in amounts within the above range, from the viewpoints of production of the resin composition and an effect of improving a thermal conductivity. On that account, the thermally conductive particle-filled fiber of the present invention preferably contains the thermally conductive particles in amounts within the above range.
[0033] The thermally conductive particle-filled fiber of the present invention has an average fiber diameter of 50 to 10000 nm, preferably 100 to 5000 nm, more preferably 100 to 1000 nm.
[0034] Here, the average fiber diameter of the thermally conductive particle-filled fiber can be measured by photographing the resulting nanofibers by a scanning type electron microscope (SU1510 manufactured by Hitachi High-Technologies Corporation) to obtain an image, selecting 50 points on the image at random and determining an average value.
[0035] The thermally conductive particle-filled fiber of the present invention preferably has an average fiber length of not less than 100 m, more preferably not less than 500 m, further preferably not less than 1000 m.
[0036] Here, the average fiber length of the thermally conductive particle-filled fiber can be measured by photographing the resulting nanofibers by a scanning type electron microscope to obtain an image, selecting 50 points on the image at random and determining an average value.
[0037] In the thermally conductive particle-filled fiber of the present invention, at least some of the thermally conductive particles are preferably present inside the fiber. That is to say, the thermally conductive particle-filled fiber of the present invention is a fine fiber in which the thermally conductive particles are dispersed. In order to obtain such a state, the thermally conductive particle-filled fiber of the present invention is preferably a fine fiber produced by an electrospinning method. The thermally conductive particle-filled fiber of the present invention can be produced by a process for producing a thermally conductive particle-filled fiber, the process having a step of spinning by an electrospinning method using a polymer solution containing a resin, thermally conductive particles and a solvent.
[0038] As the resin and the thermally conductive particles, the aforesaid ones are used. The resin is preferably a curable resin such as a thermosetting resin or a UV curable resin. The resin may be a resin having a curable group such as an epoxy group. When the resin is a curable resin, a curing agent can be contained in the polymer solution.
[0039] As the solvent in the polymer solution, a solvent that dissolves the resin is used. Examples of the solvents include organic solvents, specifically, ketones, such as methyl ethyl ketone, methyl isobutyl ketone, acetone and cyclohexanone, aromatic hydrocarbons, such as benzene, toluene, xylene and ethylbenzene, alcohols, such as methanol, ethanol, isopropyl alcohol, n-butanol and isobutyl alcohol, ethers, such as ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monobutyl ether, diethylene glycol monomethyl ether and diethylene glycol monoethyl ether, esters, such as ethyl acetate, butyl acetate, ethyl lactate, -butyrolactone, propylene glycol monomethyl ether acetate and propylene glycol monoethyl ether acetate, and amides, such as dimethylformamide, N,N-dimethylacetoacetamide and N-methylpyrrolidone. In the present invention, the polymer solution is preferably prepared by mixing a mixture of the thermally conductive particles and the solvent with the resin. The electrospinning method using the polymer solution can be carried out in accordance with a known method.
[0040] The polymer solution may contain a dispersant. Examples of the dispersants include anionic dispersants including fatty acids that include polyvalent carboxylic acids, unsaturated fatty acids and the like, polymer-based ionic dispersants, and phosphate-based compounds. The dispersant is preferably used in a ratio of 1 to 25 mass % to the thermally conductive particles.
[0041] In the present invention, it is preferable that the resin is a polymer containing an epoxy group and a curing agent therefor is used. Specifically, a combination of a polymer having a glycidyl group and an amine compound that is a curing agent can be used as the resin. More specifically, a combination of a polymer selected from polyglycidyl methacrylate and poly-bisphenol A diglycidyl ether and a chain aliphatic polyamine such as diethylenetriamine, triethylenetetramine, tetraethylenepentamine, dipropylenediamine or diethylaminopropylamine can be mentioned. The amine compound that is a curing agent is preferably used in a ratio of 1 to 10 mass % to the polymer.
[0042] In the present invention, a polymer solution containing a polymer selected from polyglycidyl methacrylate and poly-bisphenol A diglycidyl ether, a chain aliphatic polyamine that is a curing agent for the polymer, thermally conductive particles such as magnesium oxide particles, and a solvent for the polymer is preferably used in the production of the thermally conductive particle-filled fiber.
Resin Composition and Production Process for the Same
[0043] The resin composition of the present invention contains the thermally conductive particle-filled fiber of the present invention and a resin (referred to as a matrix resin hereinafter).
[0044] The matrix resin in the resin composition may be the same as or different from the resin to constitute the thermally conductive particle-filled fiber. As the matrix resin in the resin composition, one or more selected from epoxy resins, acrylic resins, amide-imide resins, phenolic resins, silicone resins and the like can be mentioned. The resin may be one having a curable group such as an epoxy group.
[0045] In one aspect, the resin composition of the present invention preferably contains thermally conductive particles in the matrix resin (the particles being referred to as particles for a matrix resin hereinafter). That is to say, in one aspect, the resin composition of the present invention preferably contains thermally conductive particles dispersed in the matrix resin. As the particles for a matrix resin, one or more selected from metal oxide particles, metal nitride particles and carbon particles can be mentioned. As the particles for a matrix resin, one or more selected from aluminum oxide particles, magnesium oxide particles and crystalline silica particles are preferable. The particles for a matrix resin may be those of the same type as the thermally conductive particles in the thermally conductive particle-filled fiber (the particles being referred to as particles for a fiber hereinafter) or those of different type from them. The average particle diameter and the content of the particles for a matrix resin can be selected according to the purpose of addition.
[0046] The resin composition of the present invention preferably contains 1 to 90 parts by mass, more preferably 25 to 80 parts by mass, further preferably 30 to 75 parts by mass, of the thermally conductive particle-filled fiber of the present invention based on 100 parts by mass of the matrix resin.
[0047] In the case of a resin composition having been improved in thermal conductivity, such composition as below can be given as one example.
[0048] Matrix resin 5 to 99 parts by mass
[0049] Particles for matrix resin 0 to 95 parts by mass
[0050] Thermally conductive particle-filled fiber of the present invention 1 to 90 parts by mass
[0051] In this resin composition, the resin is preferably a resin containing bisphenol A diglycidyl ether as a constituent monomer. The average particle diameter of the particles for a matrix resin is preferably 0.1 to 10 m. When the particles for a matrix resin are used, it is preferable to use the thermally conductive particle-filled fiber in such a manner that the amount of the particles for a fiber in the thermally conductive particle-filled fiber becomes 1 to 75 mass % based on the particles for a matrix resin. That is to say, the mass ratio of particles for a fiber/particles for a matrix resin is preferably 0.01 to 0.75.
[0052] When the resin composition of the present invention contains the matrix resin and the particles for a matrix resin, the resin composition of the present invention preferably contains 1 to 90 parts by mass, more preferably 1 to 50 parts by mass, further preferably 1 to 25 parts by mass, of the thermally conductive particle-filled fiber of the present invention, based on 100 parts by mass of the total of the matrix resin and the particles for a matrix resin.
[0053] Particles of magnesium oxide or the like are known as an additive to enhance thermal conductivity of a resin, and in the present invention, the thermally conductive particles are contained in a fine fiber to prepare a thermally conductive particle-filled fiber, and the thermally conductive particle-filled fiber is blended in the resin composition, whereby thermal conductivity is remarkably enhanced as compared with the case where the same amount of the thermally conductive particles are directly blended in the resin composition.
[0054] Examples of uses of the resin composition of the present invention include heat dissipation materials and heat exchange materials for various electronic devices.
[0055] The resin composition of the present invention preferably has a transmittance of not less than 80% T, more preferably not less than 85% T, further preferably not less than 90% T. This transmittance can be obtained as a spectral transmittance measured in an incident light wavelength region of 380 to 780 nm using a spectrophotometer. As the spectrophotometer, for example, a ratio beam spectrophotometer (manufactured by Hitachi High-Tech Science Corporation; U-5100) can be used. By using the thermally conductive particle-filled fiber of the present invention, a resin composition enhanced in thermal conductivity while maintaining transparency can be obtained.
[0056] The resin composition of the present invention can be produced by a process for producing a resin composition including step (I) of producing the thermally conductive particle-filled fiber of the present invention and step (II) of blending the thermally conductive particle-filled fiber obtained in step (I) with a resin, wherein step (I) has a step of spinning by an electrospinning method using a polymer solution containing the resin, the magnesium oxide particles and a solvent.
[0057] Step (I) is the same as the aforesaid process for producing the thermally conductive particle-filled fiber of the present invention.
[0058] In step (II), by mixing the thermally conductive particle-filled fiber with a constituent monomer of the matrix resin and polymerizing the constituent monomer, the thermally conductive particle-filled fiber can be blended in the matrix resin. Alternatively, in step (II), by kneading the thermally conductive particle-filled fiber obtained in step (I) with the matrix resin, the thermally conductive particle-filled fiber can be blended in the matrix resin.
[0059] In step (II), the particles for a matrix can be blended in the matrix resin.
[0060] In step (II), for example, by mixing the thermally conductive particle-filled fiber obtained in step (I), a constituent monomer of the matrix resin, and optionally, the particles for a matrix and polymerizing the constituent monomer, the thermally conductive particle-filled fiber and optionally the particles for a matrix can be blended in the matrix resin.
[0061] After step (II), step (III) to mold the mixture obtained in step (II) can be further provided. That is to say, a process for producing a resin molded article including step (I), step (II) and step (III) can be provided by the present invention. When a method of polymerizing the constituent monomer of the matrix resin is adopted in step (II), production of the resin composition and molding thereof can be carried out at the same time by filling a mold with the mixture for polymerization or applying the mixture to a support and then curing the mixture. For example, by mixing the thermally conductive particle-filled fiber obtained in step (I), the particles for a matrix and the constituent monomer of the matrix resin, filling a mold with the resulting mixture and polymerizing the constituent monomer in the mold, a resin composition containing the thermally conductive particle-filled fiber and the particles for a matrix can be molded. Furthermore, by curing a coating film of the mixture obtained in step (II), a thin film can be formed.
[0062] Moreover, a composite article in which the thermally conductive particle-filled fiber of the present invention or the resin composition of the present invention is combined with another member can also be obtained. An example thereof is an article in which the thermally conductive particle-filled fiber of the present invention is combined with a sheet, an adhesive film or the like.
[0063] Taking use application, etc. into consideration, the resin composition of the present invention can be molded into an appropriate shape and then used. By the present invention, a thin film composed of the resin composition of the present invention is provided. The thin film of the present invention preferably has a transmittance of not less than 80% T, more preferably not less than 85% T, further preferably not less than 90% T. This transmittance can be obtained as a spectral transmittance measured in an incident light wavelength region of 380 to 780 nm using a spectrophotometer. As the spectrophotometer, for example, a ratio beam spectrophotometer (manufactured by Hitachi High-Tech Science Corporation; U-5100) can be used. The thin film of the present invention preferably has a transmittance within the above range under the conditions of a thickness of 160 m and an incident light wavelength of 400 nm. By using the thermally conductive particle-filled fiber of the present invention, a thin film enhanced in thermal conductivity while maintaining transparency can be obtained.
[0064] By the present invention, a process for producing a molded article including mixing the thermally conductive particle-filled filled fiber of the present invention and a constituent monomer for a matrix resin and curing the monomer in the mixture is provided.
[0065] By the present invention, a process for producing a cured thin film including mixing the thermally conductive particle-filled fiber of the present invention and a constituent monomer for a matrix resin, forming the mixture into a thin film and then curing the monomer in the thin film is further provided. A method for forming the mixture into a thin film is, for example, a method of applying the mixture to a support.
EXAMPLES
Example 1 and Comparative Example 1
Production of Thermally Conductive Particle-Filled Fiber
(1) Preparation of Polymer Solution
[0066] Magnesium oxide particles (average particle diameter: 35 nm) and methyl ethyl ketone that was a solvent were mixed using a high-flex homogenizer, thereby preparing a dispersion. The concentration of the magnesium oxide particles in the dispersion was 30 mass %.
[0067] As a resin for a thermally conductive particle-filled fiber, flaky polyglycidyl methacrylate (PGMA) was used. As a curing agent for PGMA, triethylenetetramine (TETA) was used.
[0068] In the dispersion, PGMA was dissolved, and TETA was added, thereby preparing a polymer solution for use in an electrospinning method. The polymer solution had composition of 21 mass % of magnesium oxide particles, 52 mass % of methyl ethyl ketone, 25 mass % of PGMA, and 2 mass % of TETA.
(2) Production of Thermally Conductive Particle-Filled Fiber by Electrospinning Method
[0069] Using the polymer solution prepared in the above (1), electrospinning was carried out by an electrospinning device (NEU Nanofiber Electrospinning Unit, KATO TECH CO., LTD.), and methyl ethyl ketone that was the solvent was vaporized, thereby producing thermally conductive particle-filled fibers having an average fiber diameter of 497 nm. The conditions of the electrospinning device were set to: syringe rate: 0.05 mm/min, nozzle inner diameter: 1.20 mm, rotary target (collector): stainless steel drum (diameter: 10 cm), rotary target rate: 3.00 m/min, voltage applied to nozzle: +15 kV, and distance from nozzle tip to rotary target: 10 cm.
[0070] Regarding these thermally conductive particle-filled fibers, at least some of the magnesium oxide particles were present inside the fibers. After the electrospinning method, the thermally conductive particle-filled fibers had composition of 40 mass % of magnesium oxide particles, and 60 mass % of a crosslinked resin of PGMA (corresponding to 55.7 mass % of PGMA and 4.3 mass % of TETA).
Production of Film for Evaluation
[0071] The resulting thermally conductive particle-filled fibers, bisphenol A diglycidyl ether (BPADGE) that was a monomer for a matrix resin, and aluminum oxide (average particle diameter: 3 m) serving as particles for a matrix were mixed by an ultrasonic homogenizer, thereby preparing a monomer solution. To the monomer solution prepared, triethylenetetramine was added, and then the resulting mixture was poured into a Teflon (R) mold and heated at 120 C. for 3 hours, thereby producing a film for evaluation.
[0072] In Table 1, composition in which the amount of aluminum oxide (Al.sub.2O.sub.3) was 50 mass % or 90 mass % in the total amount of BPADGE and aluminum oxide was adopted. As the thermally conductive particle-filled fibers, those having a magnesium oxide particle content of 40 mass % were adopted. The film was produced by controlling the addition amount of the thermally conductive particle-filled fibers in such a manner that the addition amount of magnesium oxide in the thermally conductive particle-filled fibers based on 100 parts by mass of the total of BPADGE and aluminum oxide was as shown in Table 1. In the films of the examples, the thermally conductive particle-filled fibers and the magnesium oxide particles were dispersed in the matrix resin.
[0073] As a film for comparison, a film was produced by preparing a monomer solution using, instead of the thermally conductive particle-filled fibers, the magnesium oxide particles blended in the thermally conductive particle-filled fibers, as they were, in the addition amount of Table 1.
[0074] In the table, a combination of BPADGE and aluminum oxide is written as a matrix resin for convenience.
Evaluation of Film
[0075] Thermal diffusivity, specific heat and density of each of the resulting films for evaluation were measured, and a thermal conductivity (W/m.Math.K) was calculated from the following equation.
Thermal conductivity=(thermal diffusivityspecific heatdensity)
[0076] The thermal diffusivity was measured using a thermophysical property measuring device (Bethel Co., Ltd., Hudson Laboratory; Thermowave Analyzer TA3). At five measurement points in total, namely the center of a film in a direction perpendicular to the film and other points 1 mm shifted from the center to the left front, right front, left back and right back sides, the thermal diffusivity was measured, and a perpendicular average was calculated.
[0077] The specific heat was measured using a differential scanning calorimeter (manufactured by Shimadzu Corporation; DSC-60).
[0078] The specific gravity was measured using an electronic gravimeter (manufactured by Alfa Mirage Co., Ltd.; EW-300SG).
[0079] The results are set forth in Table 1. In Table 1, a thermal diffusivity of a film produced without adding the thermally conductive particle-filled fibers is also set forth.
[0080] In
TABLE-US-00001 TABLE 1 MgO Matrix resin Addition Al.sub.2O.sub.3 content (mass %) Addition method amount.sup.*1 50 90 Category Thermal not added 0.36 1.11 Reference conductivity Example (W/m .Math. K) MgO 40 mass %- 2 parts by 0.67 1.46 Example containing fiber mass 1-1 MgO particle 2 parts by 0.44 1.31 Comparative mass Example 1-1 MgO 40 mass %- 4 parts by 0.82 1.53 Example containing fiber mass 1-2 MgO particle 4 parts by 0.48 1.32 Comparative mass Example 1-2 .sup.*1Addition amount: amount (parts(s) by mass) of magnesium oxide particles added based on 100 parts by mass of the matrix resin (100 parts by mass of total of BPADGE and aluminum oxide)
[0081] From the results of Table 1 and
Example 2
Production of Transparent Coating Film for Evaluation
[0082] Thermally conductive particle-filled fibers (average fiber diameter: 497 nm) containing 45 mass % of magnesium oxide particles and 55 mass % of a crosslinked resin of PGMA were produced in the same manner as in the aforesaid production of thermally conductive particle-filled fibers, except that the composition of the polymer solution was changed. In these thermally conductive particle-filled fibers, at least some of the magnesium oxide particles were present inside the fibers.
[0083] The resulting thermally conductive particle-filled fibers and a polymer solution in which 60 mass % of polyglycidyl methacrylate (PGMA) that was a monomer for a matrix resin was dissolved in methyl ethyl ketone (MEK) were kneaded in a mortar to obtain a fiber-added polymer solution. The fiber-added polymer solution prepared was applied onto a cover glass by an applicator and heated at 100 C. for one hour to obtain a transparent coating film for evaluation. In this case, the transparent coating film was produced by controlling the addition amount of the thermally conductive particle-filled fibers in such a manner that the contents of PGMA and the thermally conductive particle-filled fibers in the transparent coating film were as shown in Table 2. In the transparent coating films of the examples, the thermally conductive particle-filled fibers were dispersed in the matrix resin.
Evaluation of Transparent Coating Film
[0084] A spectral transmittance of the resulting transparent coating film for evaluation was measured using a ratio beam spectrophotometer (manufactured by Hitachi High-Tech Science Corporation; U-5100, incident light wavelength : 400 nm). Further, a thermal conductivity of the resulting transparent coating film was calculated in the same manner as in Example 1. These results are set forth in Table 2. The reference example is a transparent coating film produced without adding the thermally conductive particle-filled fibers.
TABLE-US-00002 TABLE 2 Transparent coating film Composition Evaluation Matrix resin MgO 45 mass %- Content in Film Thermal (PGMA) containing fiber terms of MgO thickness Transmittance conductivity (mass %) (mass %) (mass %) (m) (% T) (W/m .Math. K) Reference 100 0 0 120 95 0.14 Example Example 2-1 90 10 4.5 106 88 0.33 2-2 80 20 9 159 80 0.46
[0085] From the results of Table 2, it can be seen that when the thermally conductive particle-filled fibers of the present invention are used, the thermal conductivity can be improved while maintaining a transmittance of the transparent coating film. It can be thought that when the film thicknesses of the transparent coating films of Examples 2-1 and 2-2 are further decreased, the transmittances are further increased.