JP6229796B2 - Thermally conductive resin composition - Google Patents

Description

  The present invention relates to a heat conductive resin composition excellent in heat conductivity and molding processability, which exhibits its properties with high efficiency by incorporating graphite having specific physical properties into a thermoplastic resin, and melts it. The present invention relates to a heat dissipation member formed by molding.

  With the miniaturization and high integration of electric / electronic devices, heat generation of mounted parts and high temperature of use environment become remarkable, and demands for improvement of heat dissipation of constituent members are increasing. In particular, components made of metals and ceramics with high thermal conductivity are currently used for heat dissipation of automobile members and high-power LEDs. However, in order to reduce weight, increase workability and flexibility in shape, high thermal conductivity is required. There is a demand for a resin material having good properties and moldability.

  As a method of imparting thermal conductivity to a resin, a method of adding a high thermal conductivity filler such as graphite is disclosed.

  Patent Document 1 discloses a resin composition having excellent thermal conductivity by adding specific graphite particles to a resin.

Patent Document 2 discloses a conductive resin composition containing a thermoplastic resin and a graphite powder having an aspect ratio of 70% or more of particles of 3 or less.
However, in the above technique, it is necessary to highly fill the filler in order to impart thermal conductivity, and there is a problem that the fluidity is extremely lowered and the molding becomes difficult in some cases.

Japanese Patent No. 5225558 JP 2001-60413 A

  The objective of this invention is providing the heat conductive resin composition excellent in heat conductivity and moldability, and a molded article containing the same.

As a result of intensive studies to solve the above problems, the present inventors have found that a resin composition containing graphite having a specific shape is excellent in thermal conductivity and moldability, and completed the present invention. It came to do. That is, this invention is following (1)-(10).
(1) (A) Thermoplastic resin 30 to 90% by mass, (B) Scale-like graphite having a volume average particle diameter of 40 to 700 μm, a fixed carbon content of 98% by mass or more, and an aspect ratio of 21 or more in the molded body. 10 to 70% by mass, a specific gravity of 1.4 to 2.0, and a thermal conductivity in the plane direction of 1 W / (m · K) or more, characterized in that object.
(2) The heat conductive resin composition is produced by melt kneading, and the flake graphite (B) before melt kneading has a volume average particle diameter of 201 to 700 μm, a fixed carbon content of 98% by mass or more, and an aspect ratio. It is 21 or more, The heat conductive resin composition as described in (1) characterized by the above-mentioned.
(3) The thermoplastic resin (A) is at least one selected from the group consisting of a polyester resin, a polycarbonate resin, a liquid crystal polyester resin, a polyamide resin, a polyphenylene sulfide resin, and a polyolefin resin. The heat conductive resin composition as described in 1) or (2).
(4) The thermal conductivity according to (3), wherein the polyester resin is at least one selected from the group consisting of polybutylene terephthalate, polyethylene terephthalate, and polyester-polyether copolymer. Resin composition.
(5) The heat conductive resin composition according to (4), wherein the polybutylene terephthalate, polyethylene terephthalate, and polyester-polyether copolymer have a number average molecular weight of 12,000 to 70,000. object.
(6) The thermal conductivity according to (3), wherein the polyamide resin is at least one selected from the group consisting of nylon 6, nylon 6, 6, nylon 4, 6, and nylon 12. Resin composition.
(7) The heat conductive resin composition according to any one of (1) to (6), wherein the scaly graphite (B) is natural graphite.
(8) A heat dissipating casing comprising the thermally conductive resin composition according to any one of (1) to (7).
(9) A heat radiating chassis comprising the thermally conductive resin composition according to any one of (1) to (7).
(10) An automotive LED lamp heat sink comprising the thermally conductive resin composition according to any one of (1) to (7).

  The heat conductive resin composition of this invention is excellent in heat conductivity and a moldability (fluidity) by containing a thermoplastic resin (A) and a specific graphite particle (B).

It is a schematic diagram which shows the structure of one Embodiment of the thermal radiation housing | casing for vehicle-mounted CCD camera accommodation. It is a schematic diagram which shows the structure of one Embodiment of a box-type thermal radiation housing | casing. It is a schematic diagram which shows the structure of one Embodiment of the heat sink for vehicle-mounted LED lamp accommodation. It is a schematic diagram which shows the structure of another embodiment of the heat sink for vehicle-mounted LED lamp accommodation. It is a schematic diagram which shows the structure of the heat sink of another form.

  The content of the thermoplastic resin (A) of the present invention is 30 to 90% by mass, preferably 30 to 80% by mass, more preferably 35 to 50% by mass, when the heat conductive resin composition is 100% by mass. 75% by mass. When the thermoplastic resin (A) is less than 30% by mass, molding processability is remarkably deteriorated, so that molding may be difficult. When it exceeds 90% by mass, excellent thermal conductivity may not be exhibited.

  The flaky graphite (B) used in the present invention is graphite particles having specific physical properties. That is, the volume average particle diameter of the scaly graphite (B) in the molded body made of the heat conductive resin composition of the present invention is 40 to 700 μm, more preferably 50 to 500 μm, and still more preferably 50 to 300 μm. When the volume average particle diameter is less than 40 μm, the thermal conductivity of the resin composition is lowered. Moreover, although the thermal conductivity tends to improve as the particle size increases, the strength of the resin composition may decrease when it exceeds 300 μm. The volume average particle diameter can be measured by a laser diffraction method, a light scattering method, or the like.

  The fixed carbon content of the flaky graphite (B) in the molded body made of the heat conductive resin composition of the present invention is 98% by mass or more, preferably 98.5% by mass or more, and more preferably 99% by mass or more. When the amount of fixed carbon is less than 98% by mass, the thermal conductivity tends to decrease. The amount of fixed carbon can be measured according to JIS M8511.

  The aspect ratio of the scaly graphite (B) is 21 or more in the molded body made of the heat conductive resin composition of the present invention. The upper limit of the aspect ratio is preferably as high as possible, and is not particularly limited. However, if the upper limit is set, the preferred range is 1,000,000 or less, the more preferred range is 5,000 or less, and even more preferred. 3,000 or less. The aspect ratio can be calculated from the maximum diameter / thickness by measuring each length of the maximum diameter and thickness with an electron microscope or the like.

The particle size distribution before the melt-kneading of the flaky graphite (B) or in the molded body is not particularly limited, but if limited, the cumulative volumes obtained by measuring the particle size distribution are 20% and 80%, respectively. The ratio D ₈₀ / D ₂₀ of the particle diameters D ₂₀ and D ₈₀ is preferably 1 to 20, more preferably 1 to 10, and still more preferably 1 to 5.

  The content of the scaly graphite (B) of the present invention is 10 to 70% by mass, preferably 15 to 65% by mass, more preferably 20 to 20%, when the heat conductive resin composition is 100% by mass. 60% by mass.

  The heat conductive resin composition of this invention is manufactured by melt-kneading a thermoplastic resin (A), scale-like graphite (B), and other components. The larger the volume average particle diameter of the flaky graphite (B) before melt kneading, the better, preferably 201 to 700 μm, more preferably 230 to 650 μm, and further preferably 250 to 400 μm. The aspect ratio is preferably 21 or more. The upper limit of the aspect ratio is preferably as high as possible, and is not particularly limited. However, if an upper limit is set, a preferable range is 3,000 or less, a more preferable range is 1,000 or less, and more preferably. 500 or less. The amount of fixed carbon shall not change before and after melt-kneading or molding. Generally, graphite tends to be crushed during melt-kneading and molding. Therefore, the larger the volume-average particle size of graphite before melt-kneading, the larger the volume-average particle size of graphite after melt-kneading and molding. Largely held, heat conductivity and moldability are improved.

  The specific gravity of the heat conductive resin composition of this invention is 1.4-2.0, More preferably, it is 1.5-1.9.

  The “surface direction thermal conductivity” as used in the present invention refers to the thermal conductivity in the direction in which the molten resin flows when a molded body is produced. The thermal conductivity in the direction perpendicular to the resin flow direction is referred to as “thickness direction thermal conductivity”. The thermal conductivity in the surface direction of the thermally conductive resin composition of the present invention is 1 W / (m · K) or more, preferably 3 W / (m · K) or more, more preferably 5 W / (m · K). K) or more. The upper limit is not particularly limited, and the higher the better.

  The thermal conductivity in the thickness direction of the thermally conductive resin composition of the present invention is not particularly limited, and the higher the better. If a lower limit is set, it is preferably 0.5 W / (m · K) or more, more preferably 0.8 W / (m · K) or more, and further preferably 1 W / (m · K). That's it.

Examples of the thermoplastic resin (A) used in the present invention include aromatic vinyl resins such as polystyrene, vinyl cyanide resins such as polyacrylonitrile, chlorine resins such as polyvinyl chloride, and polymethacrylic acid such as polymethyl methacrylate. Ester resins, polyacrylate resins, polyolefin resins such as polyethylene, polypropylene and cyclic polyolefin resins, polyvinyl ester resins such as polyvinyl acetate, polyvinyl alcohol resins and their derivative resins, polymethacrylate resins, Polyacrylic acid resins and their metal salt resins, polyconjugated diene resins, polymers obtained by polymerizing maleic acid and fumaric acid and their derivatives, polymers obtained by polymerizing maleimide compounds, amorphous Semi-aromatic polyester and amorphous all Non-crystalline polyester resins such as aromatic polyesters, crystalline polyester resins such as crystalline semi-aromatic polyesters and crystalline wholly aromatic polyesters, aliphatic polyamides, aliphatic-aromatic polyamides, wholly aromatic polyamides, etc. Polyamide resin, polycarbonate resin, polyurethane resin, polysulfone resin, polyalkylene oxide resin, cellulose resin, polyphenylene ether resin, polyphenylene sulfide resin, polyketone resin, polyimide resin, polyamideimide resin, poly Etherimide resins, polyether ketone resins, polyether ether ketone resins, polyvinyl ether resins, phenoxy resins, fluorine resins, silicone resins, liquid crystal polymers, and runs of these exemplified polymers Arm block graft copolymer, and the like. These thermoplastic resins can be used alone or in combination of two or more. When two or more kinds of resins are used in combination, a compatibilizing agent or the like can be added as necessary. These thermoplastic resins (A) may be properly used depending on the purpose.
Among these thermoplastic resins, preferred thermoplastic resins include polyester resins, polycarbonate resins, liquid crystal polyester resins, polyamide resins, polyphenylene sulfide resins, and polyolefin resins.

  Further, among thermoplastic resins, part or all of the resin is a thermoplastic resin having crystallinity or liquid crystallinity, and the thermal conductivity of the obtained resin composition tends to be high. It is preferable from the viewpoint of easy inclusion of graphite in the resin. These thermoplastic resins having crystallinity or liquid crystallinity are part of the resin such that only a specific block in the molecule of the block or graft copolymer resin is crystalline or liquid crystalline even if the entire resin is crystalline. Only may be crystalline or liquid crystalline. There is no particular limitation on the crystallinity of the resin. Further, as the thermoplastic resin, a polymer alloy of an amorphous resin and a crystalline or liquid crystalline resin can be used. There is no particular limitation on the crystallinity of the resin.

  Some thermoplastic resins, which are part or all of crystalline or liquid crystalline, can be crystallized, but can be used alone or molded under specific molding conditions. Some resins exhibit amorphous properties. When such a resin is used, there is a case where a part or the whole of the resin can be crystallized by devising a molding method such as stretching or post-crystallization.

  Among the thermoplastic resins having crystallinity or liquid crystallinity, preferred resins include crystalline polyester resin, crystalline polyamide resin, polyphenylene sulfide resin, liquid crystal polymer, crystalline polyolefin resin, polyolefin block copolymer, etc. However, the present invention is not limited to these, and various crystalline resins and liquid crystalline resins can be used. Specific examples of the crystalline polyester include polyethylene terephthalate, polypropylene terephthalate, polybutylene terephthalate, polyethylene-2,6-naphthalate, polybutylene naphthalate, poly 1,4-cyclohexylenedimethylene terephthalate and polyethylene-1,2-bis ( Phenoxy) ethane-4,4'-dicarboxylate, etc., polyethylene isophthalate / terephthalate, polybutylene terephthalate / isophthalate, polybutylene terephthalate / decane dicarboxylate and polycyclohexanedimethylene terephthalate / isophthalate, polyester / poly Examples thereof include crystalline copolyesters such as ether.

  The polyester / polyether (hereinafter referred to as a polyester-polyether copolymer) is represented by 50 to 80% by weight of an aromatic polyester unit and the following general formula (1) from the viewpoint of moldability and heat resistance, and will be described later. It is preferably a polymer comprising 20 to 50% by weight of a modified polyether unit, more preferably a polymer comprising 60 to 80% by weight of an aromatic polyester unit and 20 to 40% by weight of the modified polyether unit. .

(In the general formula (1), -A- is, -O -, - S -, - SO -, - SO 2 -, - CO-, an alkylene group having 1 to 20 carbon atoms or 6 to 20 carbon atoms, An alkylidene group, R ¹ , R ² , R ³ , R ⁴ , R ⁵ , R ⁶ , R ⁷ , and R ⁸ are all hydrogen atoms, halogen atoms, or monovalent carbon atoms having 1 to 5 carbon atoms. Each of R ⁹ and R ¹⁰ is a divalent hydrocarbon group having 1 to 5 carbon atoms, which may be the same or different, and m and n are oxyalkylene units. Indicates the number of repeating units, and 2 ≦ m + n ≦ 50.)

  A polyester-polyether copolymer is produced by using a catalyst to which an antimony compound, and optionally a germanium compound, is added, (1) a three-way direct esterification method of an aromatic dicarboxylic acid, a diol, and a modified polyether, 2) Three-way transesterification method of dialkyl aromatic dicarboxylate, diol, modified polyether, and / or ester of modified polyether, (3) Dialkyl aromatic dicarboxylate, during transesterification of diol, or transesterification Examples include, but are not limited to, a method of polycondensation by adding a modified polyether later, and a method of (4) transesterification under a melt and reduced pressure after mixing with a modified polyether using a polymeric aromatic polyester. Although not intended, the production method (4) is preferred from the viewpoint of composition controllability.

  Examples of the antimony compound used as the catalyst according to the present invention include antimony trioxide, antimony pentoxide, antimony acetate, antimony glycoxide and the like, and these are used alone or in combination of two or more. Of these antimony compounds, antimony trioxide is particularly preferred. The amount of the antimony compound catalyst to be added at the time of polymerization is preferably 50 to 2000 ppm by weight of resin, more preferably 100 to 1000 ppm by weight, from the viewpoint of reaction rate and economical viewpoint.

  Examples of germanium compounds used as the catalyst include germanium oxide such as germanium dioxide, germanium alkoxide such as germanium tetraethoxide and germanium tetraisopropoxide, germanium hydroxide and its alkali metal salts, germanium glycolate, germanium chloride, acetic acid. Germanium etc. are mentioned, These are used individually or in combination of 2 or more types. Of these germanium compounds, germanium dioxide is particularly preferred. The amount of germanium dioxide catalyst to be introduced at the time of polymerization is preferably 50 to 2000 ppm by weight of resin, more preferably 100 to 1000 ppm by weight, from the viewpoint of reaction rate and economical viewpoint.

  The aromatic dicarboxylic acid is particularly preferably terephthalic acid, and other examples include isophthalic acid, diphenyldicarboxylic acid, and diphenoxyethanedicarboxylic acid. In addition to these aromatic dicarboxylic acids, a small proportion (15% or less) of other aromatic oxycarboxylic acids such as oxybenzoic acid, or aliphatics such as adipic acid, sebacic acid, cyclohexane 1,4-dicarboxylic acid, Or you may use together alicyclic dicarboxylic acid.

  The diol is a low molecular weight glycol component that forms an ester unit, and is a low molecular weight glycol having 2 to 10 carbon atoms, such as ethylene glycol, trimethylene glycol, tetramethylene glycol, hexanediol, decanediol, cyclohexanedimethanol, etc. is there. In particular, ethylene glycol, trimethylene glycol, and tetramethylene glycol are preferable from the viewpoint of availability.

  As the alkyl group of the dialkyl aromatic dicarboxylate, a methyl group is preferable from the viewpoint of transesterification.

  The solution viscosity of the high-molecular aromatic polyester is 25 in a mixed solvent of phenol / tetrachloroethane = 1/1 (weight ratio) from the viewpoint of impact resistance, chemical resistance and molding processability of the obtained molded product. The logarithmic viscosity (IV) at a concentration of 0.5 g / dl at 0 ° C. is preferably in the range of 0.3 to 2.0, more preferably in the range of 0.5 to 1.5.

(Aromatic polyester unit)
The aromatic polyester unit is a polymer or copolymer obtained from an aromatic dicarboxylic acid or an ester-forming derivative thereof and a diol or an ester-forming derivative thereof, and is usually an alternating polycondensate, preferably And at least one selected from the group consisting of polyethylene terephthalate units, polybutylene terephthalate units, and polypropylene terephthalate units.

  Preferable specific examples of the aromatic polyester unit include polyethylene terephthalate, polyethylene terephthalate copolymer, polybutylene terephthalate, polybutylene terephthalate copolymer, polypropylene terephthalate, or polypropylene terephthalate copolymer, more preferably polyethylene. One or more selected from the group consisting of terephthalate, polybutylene terephthalate, and polypropylene terephthalate.

(Modified polyether unit)
The modified polyether unit is a unit represented by the general formula (1), and the number average of (m + n) is preferably about m and n as the number of repeating units of the oxyalkylene unit in the general formula (1). It is 2-50, More preferably, it is 10-50, More preferably, it is 18-50.

(In the general formula (1), -A-, R ^{1 to} R ⁸ , R ^{9 to} R ¹⁰ , m and n are the same as above.)

  From the viewpoint of easy availability, the modified polyether unit is preferably a unit represented by the following general formula (2). When (m + n) is 2, the formula weight is 314, and (m + n) is 50. In this case, the formula weight is 2426. Therefore, the preferred molecular weight when introducing the unit represented by the general formula (2) as a molecule into the polyester-polyether copolymer according to the present invention is 316 to 2430, more preferably 670 to 2430, Preferably it is 1020-2430 or less, More preferably, it is 1330-2000.

  Among these crystalline polyesters, polyethylene terephthalate, polypropylene terephthalate, polybutylene terephthalate, polyethylene-2,6-naphthalate, polybutylene naphthalate, poly 1,4-cyclohexylene diene are used from the viewpoints of moldability and mechanical properties. Methylene terephthalate, polyester-polyether copolymer and the like are preferably used, and polybutylene terephthalate, polyethylene terephthalate, and polyester-polyether copolymer are more preferable from the viewpoint of being inexpensive and easily available.

  The number average molecular weight of the present invention is a high temperature GPC using a solution prepared by dissolving polystyrene in a mixed solvent of p-chlorophenol and toluene in a volume ratio of 3: 8 so as to have a concentration of 2.5% by weight. (Viscotek: 350 HT-GPC System) is a value measured at a column temperature of 80 ° C. and a detector as a differential refractometer (RI).

  The number average molecular weight of the polybutylene terephthalate, polyethylene terephthalate, and polyester-polyether copolymer is preferably 12,000 to 70,000, more preferably 15,000 to 60,000, and 20,000. Particularly preferred is ˜50,000. If it is less than 12,000, the mechanical strength may be low, and if it is greater than 70,000, molding may be difficult.

  Specific examples of the crystalline polyamide resin include, for example, ring-opening polymer of cyclic lactam, polycondensate of aminocarboxylic acid, polycondensate of dicarboxylic acid and diamine, and specifically nylon 6, nylon. 4, 6, Nylon 6, 6, Nylon 6, 10, Nylon 6, 12, Nylon 11, Nylon 12, and other aliphatic polyamides, poly (metaxylene adipamide), poly (hexamethylene terephthalamide), poly (hexa Methylene isophthalamide), polynonanemethylene terephthalamide, poly (tetramethylene isophthalamide), poly (methylpentamethylene terephthalamide) and other aliphatic-aromatic polyamides, and copolymers thereof. For example, nylon 6 / poly (hexamethylene terephthalamide), Niro 6.6 / poly (hexamethylene terephthalamide), nylon 6 / nylon 6.6 / poly (hexamethylene isophthalamide), poly (hexamethylene isophthalamide) / poly (hexamethylene terephthalamide), nylon 6 / poly (hexa) And methylene isophthalamide) / poly (hexamethylene terephthalamide), nylon 12 / poly (hexamethylene terephthalamide), poly (methylpentamethylene terephthalamide) / poly (hexamethylene terephthalamide), and the like. The form of copolymerization may be either random or block, but is preferably a random copolymer from the viewpoint of moldability.

  Among crystalline polyamide resins, nylon 6, nylon 6,6, nylon 12, nylon 4,6, nylon 6T, nylon 9T, polynonamethylene terephthalamide, nylon 6 from the viewpoints of moldability and mechanical properties / Poly (hexamethylene terephthalamide), nylon 6/6 / poly (hexamethylene terephthalamide), nylon 6 / nylon 6.6 / poly (hexamethylene isophthalamide), poly (hexamethylene isophthalamide) / poly (hexamethylene) Terephthalamide), nylon 6 / poly (hexamethylene isophthalamide) / poly (hexamethylene terephthalamide), nylon 12 / poly (hexamethylene terephthalamide), nylon 6 / nylon 6.6 / poly (hexamethylene isophthalamide), Poly Methyl pentamethylene terephthalamide) / poly (hexamethylene terephthalamide) polyamides such, it is preferable to use the like, more preferably, nylon 6, nylon 6 · 6, nylon 4.6, nylon 12.

  The number average molecular weight of the polyamide is not particularly limited, but is preferably 12,000 or more from the viewpoint of strength.

  The scaly graphite used in the present invention may be either natural graphite or artificial graphite, and may be used in combination, but natural graphite is preferred from the viewpoint that it can be obtained at a low cost. Further, either α-graphite or β-graphite may be used, or these may be combined.

  As graphite used in the present invention, graphite having other particle diameters, shapes, and characteristics may be used in combination as long as the physical properties of the present invention are not significantly impaired. Specific examples of the shape include fiber, lump, earth, and sphere.

  Since the thermally conductive resin composition of the present invention has excellent thermal conductivity, molding processability, and low specific gravity, a molded body made of the composition is suitable for a heat radiating structural member. Specific examples of these include, for example, a heat radiating housing and a heat radiating chassis. The heat dissipating casing of the present invention is used with a heating element housed therein. The heating element may be a thing that is exothermic per se or a substance that generates heat when heated from the outside. Typical heating elements are exothermic parts or equipment (devices), for example, electronic parts such as LD (laser diode) and IC (integrated circuit), electronic equipment using computers such as personal computers, word processors and video games. , Engine control unit (ECU) which is a computer that determines fuel injection amount and ignition timing based on information such as air intake amount and throttle opening to automobile engine, LED lamp lighting, inverter, automotive lamp housing , A heat radiating casing for various uses such as a coil, a bobbin, a connector, a bus bar, and a power steering.

  In addition, the heat dissipation chassis of the present invention is used as a key chassis or subchassis to release heat from the heating element. A typical example of the heating element is a heat-generating component that itself is a heating element, and specific examples thereof include electronic components such as LDs and ICs in electronic and electrical products such as mobile phones and TVs. . These are used by being mounted (fixed) on the heat-dissipating chassis, and are not fixed to the heat-dissipating chassis, but are arranged in contact or close to each other. The heat dissipating chassis of the present invention is also suitably used as an LED (light emitting diode) lighting package.

  The molded body made of the heat conductive resin composition of the present invention is also suitable for LED lamp heat sinks for automobiles, and can be designed freely in shape as compared to metal, and can be made fuel efficient by reducing weight. It can lead to improvement. The automobile LED lamp heat sink of the present invention refers to a heat sink for cooling the LED module. Automotive LED lamps include interior lamps and exterior lamps, such as room lamps, map lamps, head lamps, fog lamps, front turn signal lamps, front positioning lamps, side turn signal lamps, day lamps, fog lamps, tail lamps, stop lamps, Examples include rear turn signal lamps, high-mount stop lamps, back lamps, and license plate lamps.

The heat dissipating case, the heat dissipating chassis, and the automobile LED lamp heat sink, which are the heat dissipating structural members of the present invention, do not need to use the heat conductive resin composition of the present invention on the entire surface or the entire interior, and are adapted to the intended use. Other materials may be partially configured, and holes may be provided on any surface. Specifically, ceramics, an insulating resin, and a resin composition may be combined to provide insulating properties, and in order to improve heat dissipation, a metal, graphite sheet, or carbon fiber composite is partially used. A good heat conductor such as a material may be combined. Although these installation locations are not particularly limited, the good heat conductor is preferably installed between the heating element and the heat conductive resin composition.
The material of the metal member for further enhancing the heat dissipation is not particularly limited, but aluminum and alloys including the same (aluminum alloy), copper and alloys including the same (brass, bronze, aluminum brass, etc.), nickel, chromium, Examples thereof include titanium, iron, cobalt, tin, zinc, palladium, silver, stainless steel, magnesium and an alloy containing the same (magnesium alloy), manganese, and the like.

  The shape of the metal member is not particularly limited, and examples thereof include a flat plate shape, a curved plate shape, a rod shape, a cylindrical shape, and a lump shape, and may be a structure formed by a combination thereof. Moreover, you may have a through-hole, a bending part, etc.

When the heat radiating structural member of the present invention is composed of a metal member and a resin molded part provided on the surface thereof and made of the heat conductive resin composition of the present invention, the metal molded part is formed. Although the surface shape of a member is not specifically limited, A flat plate, a curved surface, an uneven surface, a pointed part, etc. are mentioned.
The surface of the metal member on which the resin molded part is formed may be subjected to a surface treatment from the viewpoints of adhesive strength and adhesion between the metal member and the resin molded part. The surface treatment method is not particularly limited, and examples thereof include fine chemical roughening by special chemicals and physical polishing, anodization, and formation of a film by an organic compound.

  The heat conductive resin composition of the present invention is also excellent in electromagnetic wave shielding properties, and the electromagnetic wave shielding effect at a frequency of 100 MHz is 5 dB or more, preferably 10 dB or more, and more preferably 15 to 60 dB.

  1 to 5 show an embodiment of the heat dissipating structural member of the present invention, and do not limit the heat dissipating structural member of the present invention. In addition, the dimension of the structural member for heat dissipation of this invention is not restrict | limited in particular, According to the use of this structural member, the kind of heat generating body accommodated in this structural member, a thermal radiation behavior, etc., it selects suitably. Moreover, it can use together with a metal member from a viewpoint of improving heat dissipation further.

  1A and 1B are schematic views showing the configuration of an embodiment of a heat dissipating housing 1 for storing an in-vehicle CCD camera, in which FIG. 1A is a perspective view, and FIG. 1B is a cross section taken along the line XX in FIG. FIG. The heat dissipating casing 1 is a molded article made of the heat conductive resin composition of the present invention, and is integrally formed so as to extend in the same direction as the first cylindrical body 10 having a substantially square shape in cross-section extending in the lateral direction. The second cylinder 11 is smaller in diameter than the first cylinder 10, and protrudes from one and the other surfaces 10a and 10b in the vertical direction of the first cylinder 10, and is spaced apart from the first cylinder 10 and is the same as the first cylinder 10 A plurality of first and second radiation fins 12, 13 extending in the direction. An in-vehicle CCD camera is accommodated in the internal space 10 x of the first cylinder 10, and the CCD camera is electrically connected via the internal space 11 x of the second cylinder 11. The cross-sectional shape of the first and second cylinders 10 and 11 is not limited to a square, and may be any shape such as a circle, a polygon, etc., depending on the shape of the heating element stored in the internal space 10x of the first cylinder 10. It can be a shape. Moreover, although the number of the 1st, 2nd radiation fins 12 and 13 of this embodiment is 4, respectively, it is not limited to this, It can be made into arbitrary numbers.

  2A and 2B are schematic views showing the configuration of an embodiment of the box-type heat radiating housing 2, wherein FIG. 2A is a perspective view with the opening 14 facing downward, and FIG. 2B is an X of FIG. It is sectional drawing in a -X cut surface. The heat radiating housing 2 is a molded body made of the heat conductive resin composition of the present invention, and has a substantially rectangular parallelepiped main body 15 having an opening 14 on one surface, and a surface 15a facing the opening 14 of the main body 15. The heat dissipating fins 16 and 17 are provided so as to stand in the vicinity of both ends in the longitudinal direction and extend in the width direction of the main body 15 while being spaced apart from each other. The box-type heat radiating housing 2 is used, for example, for a DRL (daytime running lamp) for automobile lamps. A heating element is housed in the internal space 15x of the main body 15. When it is necessary to electrically connect the heating elements, for example, a through hole (not shown) from the surface 15a to the internal space 15x is appropriately formed. This is common to the heat dissipating structural member of the present invention.

  FIGS. 3A and 3B are schematic views showing the configuration of an embodiment of the heat sink 3 for housing an in-vehicle LED lamp. FIG. 3A is a perspective view, and FIG. 3B is a cross-sectional view taken along the line XX in FIG. is there. The heat sink 3 is a molded body made of the thermally conductive resin composition of the present invention, and includes a support plate 18, a frame body 19 having a substantially square shape in cross section, which is erected from one surface 18 a of the support plate 18, and a support plate. And a plurality of radiating fins 20 provided so as to hang from the other surface 18b of the 18 and substantially parallel to each other. The joint portion between the heat radiating fins 20a, 20b at one end and the support plate 18 and the support plate 18 is a cross section that protrudes from the heat radiating fins 20a, 20b toward the adjacent heat radiating fins 20, for example, for the purpose of improving the bonding strength or heat radiating speed. The ribs 21a and 21b are substantially square in shape. A heating element such as an in-vehicle LED lamp is accommodated in an internal space 19a formed by the support plate 18 and the frame 19.

  FIGS. 4A and 4B are schematic views showing the configuration of an in-vehicle LED lamp housing heat sink 4 according to another embodiment, wherein FIG. 4A is a perspective view, and FIG. 4B is a cross-sectional view taken along the line XX in FIG. It is. The heat sink 4 has the same configuration as the heat sink 3 except that it does not have the ribs 21a and 21b.

  5A and 5B are schematic views showing the configuration of the heat sink 5 of another embodiment, in which FIG. 5A is a perspective view, FIG. 5B is a top view, and FIG. 5C is a cross-sectional view taken along the line XX. The heat sink 5 has a feature that it can be easily combined with, for example, a metal member. The heat sink 5 is a molded body made of the heat conductive resin composition of the present invention, and is provided on a substantially rectangular support plate 22 and one surface 22a of the support plate 22, and is a heating element, a metal member, or a heating element. And a substantially rectangular recess 23 in which a composite of the metal member (both not shown) is accommodated, and both end sides 23a and 23b in one direction of the recess 23, and a heating element, a metal member, or a heat generation The protrusions 24a and 24b for fixing the composite of the body and the metal member to the recess 23 and the other surface 22b of the support plate 22 hang down from each other, and the thickness gradually decreases toward the tip side. A plurality of plate-like heat radiation fins 25. For example, after placing the heating element, the metal member, or the composite body in the recess 23, the both ends 23 a and 23 b of the recess 23 are thermally caulked with heat, ultrasonic waves, vibrations, etc. Can be fixed and installed. Further, by disposing a heat dissipation material that reduces thermal resistance, such as TIM (thermal interface material), between the heating element, the metal member or the composite and the recess 23, the heat dissipation can be further improved. it can. By providing the radiation fins 25, combined with the high thermal conductivity of the thermally conductive resin composition of the present invention, the heat generated from the heating element can be radiated very efficiently. The three-dimensional shape of the heat sink 5 of the present embodiment is a quadrangular prism shape, but is not limited to this, and depending on the use of the heat sink, any shape such as a sphere, a polygonal column other than a quadrangular column, a cylinder, an elliptical column, and the like can do. Further, the planar shape of the recess 23 is not particularly limited, and may be a circle, an ellipse, a polygon other than a rectangle, or the like. Further, the number of the heat radiation fins 25 is not particularly limited.

  The heat conductive resin composition of the present invention has a thermoplastic resin (A) and scaly graphite (B), a heat conductive filler other than scaly graphite (B), and heat conductivity within a range that does not impair the effect. It can contain at least one selected from the group consisting of fillers other than fillers, resins, and additives. The shape of the thermally conductive filler and filler other than the flaky graphite (B) is not particularly limited, and for example, flaky, fibrous, flaky, plate-like, spherical, particulate, particulate, nanoparticle, agglomerated Examples include various shapes such as particles, tubes, nanotubes, wires, rods, irregular shapes, rugby balls, hexahedrons, composite particles in which large particles and fine particles are combined, and liquids. Specific examples of the thermally conductive filler other than the flake graphite (B) include a metal filler such as aluminum and nickel, a low melting point alloy having a liquidus temperature of 300 ° C. or higher and a solidus temperature of 150 ° C. or higher and 250 ° C. or lower. Metal oxides such as aluminum oxide, magnesium oxide, silicon oxide, beryllium oxide, copper oxide, cuprous oxide, metal nitrides such as aluminum nitride and silicon nitride, metal carbides such as silicon carbide, metal carbonates such as magnesium carbonate Insulating carbon materials such as diamond, metal hydroxides such as aluminum hydroxide and magnesium hydroxide, alumina, boron nitride, glass fiber, carbon fiber, potassium titanate whisker, silicon nitride fiber, carbon nanotube, talc, wollast A knight is mentioned and these 1 type (s) or 2 or more types can be used. Although it does not specifically limit as an addition amount, Thermal conductivity can be improved as the addition amount increases. The heat conductive filler other than the scale-like graphite (B) may be a natural product or may be synthesized. In the case of a natural product, there are no particular limitations on the production area and the like, which can be selected as appropriate.

  In the resin composition of the present invention, known fillers can be widely used depending on the purpose in addition to the heat conductive filler. Examples of fillers other than the thermally conductive filler include diatomaceous earth powder, basic magnesium silicate, calcined clay, fine powder silica, quartz powder, crystalline silica, kaolin, antimony trioxide, fine powder mica, molybdenum disulfide, rock Examples thereof include inorganic fibers such as wool, ceramic fibers, and asbestos, and glass fillers such as glass fibers, glass powder, glass cloth, and fused silica. By using these fillers, for example, it is possible to improve favorable characteristics in applying a resin composition such as thermal conductivity, mechanical strength, or abrasion resistance. Furthermore, if necessary, organic fillers such as paper, pulp, wood, polyamide fiber, aramid fiber, boron fiber and other synthetic fibers, polyolefin powder and the like can be used in combination.

  The conductive filler used in the present invention and fillers other than the conductive filler are used for improving the adhesion at the interface between the resin and the filler, and for facilitating workability. For example, silane treatment agents, stearic acid, acrylic monomers, etc. The surface treatment may be performed with various surface treatment agents. It does not specifically limit as a surface treating agent, For example, conventionally well-known things, such as a silane coupling agent and a titanate coupling agent, can be used. Among them, an epoxy group-containing silane coupling agent such as epoxy silane, an amino group-containing silane coupling agent such as aminosilane, polyoxyethylene silane, and the like are preferable because they hardly reduce the physical properties of the resin. The surface treatment method for the filler is not particularly limited, and a normal treatment method can be used.

In the thermally conductive resin composition of the present invention, at least one resin selected from the group consisting of thermoplastic resins other than the thermoplastic resin (A) and thermosetting resins may be alloyed. Specific examples of the resin include epoxy resin, polyolefin resin, bismaleimide resin, polyimide resin, polyether resin, phenol resin, silicone resin, polycarbonate resin, polyamide resin, polyester resin, fluorine resin, acrylic resin, melamine resin, urea Examples thereof include resins and urethane resins.
In the heat conductive resin composition of the present invention, as an additive other than the above resin and filler, any other components depending on the purpose, for example, reinforcing agent, heat stabilizer, antioxidant, ultraviolet absorber, aging At least one additive selected from the group consisting of an inhibitor, a thickener, a release agent, a plasticizer, a coupling agent, a flame retardant, a flame retardant aid, a flame retardant, a colorant, and a colorant, and the like Auxiliaries and the like can be added as long as the effects of the present invention are not lost. It is preferable that the usage-amount of these additives and other adjuvants is the range of 0-20 weight part in total with respect to 100 weight part of thermoplastic resins (A).

  Examples of the heat stabilizer include phosphites, hindered phenols, thioethers, and the like. These can be used alone or in combination of two or more.

  Examples of the antioxidant include phosphites, hindered amines, hydroquinones, hindered phenols, sulfur-containing compounds and the like. These can be used alone or in combination of two or more.

  Examples of the ultraviolet absorber include benzophenones, benzotriazoles, salicylic acid esters, metal complex salts and the like. These can be used alone or in combination of two or more.

  Examples of the flame retardant include organic flame retardants, inorganic flame retardants, and reactive flame retardants. These can be used alone or in combination of two or more.

  Organic flame retardants include brominated epoxy compounds, brominated alkyltriazine compounds, brominated bisphenol epoxy resins, brominated bisphenol phenoxy resins, brominated bisphenol polycarbonate resins, brominated polystyrene resins, brominated crosslinked polystyrene resins Halogenated flame retardants such as brominated bisphenol cyanurate resin, brominated polyphenylene ether, brominated bismaleimide, decabromodiphenyl oxide, tetrabromobisphenol A and oligomers thereof; trimethyl phosphate, triethyl phosphate, tripropyl phosphate, tributyl phosphate, Tripentyl phosphate, toxyl phosphate, tricyclohexyl phosphate, triphenyl phosphate, tricresyl phosphate , Trixylenyl phosphate, cresyl diphenyl phosphate, dicresyl phenyl phosphate, dimethyl ethyl phosphate, methyl dibutyl phosphate, ethyl dipropyl phosphate, hydroxyphenyl diphenyl phosphate and the like, and compounds obtained by modifying these with various substituents, Phosphorus flame retardants such as various condensed phosphate compounds, phosphazene derivatives containing phosphorus elements and nitrogen elements; polytetrafluoroethylene and the like. These can be used alone or in combination of two or more.

  Examples of the inorganic flame retardant include aluminum hydroxide, antimony oxide, magnesium hydroxide, zinc borate, zirconium-based, molybdenum-based, zinc stannate, guanidine salt, silicone-based, and phosphazene-based compounds. These can be used alone or in combination of two or more.

  Reactive flame retardants include tetrabromobisphenol A, dibromophenol glycidyl ether, brominated aromatic triazine, tribromophenol, tetrabromophthalate, tetrachlorophthalic anhydride, dibromoneopentyl glycol, poly (pentabromobenzyl polyacrylate) , Chlorendic acid (hett acid), chlorendic anhydride (hett acid anhydride), brominated phenol glycidyl ether, dibromocresyl glycidyl ether, the following general formula (3) (wherein n is an integer of 2 to 20) And organic phosphorus flame retardants represented. These can be used alone or in combination of two or more.

  In addition, when making the composition of this invention contain a flame retardant, it is preferable to use a flame retardant adjuvant. As this flame retardant aid, antimony trioxide, antimony tetroxide, antimony pentoxide, sodium antimonate, antimony tartrate and other antimony compounds, zinc borate, barium metaborate, hydrated alumina, zirconium oxide, Examples thereof include ammonium polyphosphate, tin oxide, and iron oxide. These can be used alone or in combination of two or more. Moreover, in order to improve a flame retardance, a silicone oil can be mix | blended. Moreover, the compound of the following general formula (3) can also be used.

  Examples of the antiaging agent include naphthylamine compounds, diphenylamine compounds, p-phenylenediamine compounds, quinoline compounds, hydroquinone derivative compounds, monophenol compounds, bisphenol compounds, trisphenol compounds, polyphenol compounds. Thiobisphenol compound, hindered phenol compound, phosphite compound, imidazole compound, nickel dithiocarbamate salt compound, phosphate compound and the like. These can be used alone or in combination of two or more.

  Examples of the plasticizer include phthalates such as dimethyl phthalate, diethyl phthalate, dibutyl phthalate, diisobutyl phthalate, dioctyl phthalate, butyl octyl phthalate, di- (2-ethylhexyl) phthalate, diisooctyl phthalate, and diisodecyl phthalate; dimethyl adipate , Diisobutyl adipate, di- (2-ethylhexyl) adipate, diisooctyl adipate, diisodecyl adipate, octyl decyl adipate, di- (2-ethylhexyl) azelate, diisooctyl azelate, diisobutyl azelate, dibutyl sebacate, di- Fatty acid esters such as (2-ethylhexyl) sebacate, diisooctyl sebacate; trimellitic acid isodecyl ester, trimellitic acid octy Esters, trimellitic acid esters such as trimellitic acid n-octyl ester, trimellitic acid isononyl ester; di- (2-ethylhexyl) fumarate, diethylene glycol monooleate, glyceryl monoricinolate, trilauryl phosphate, tristearyl phosphate , Tri- (2-ethylhexyl) phosphate, epoxidized soybean oil, polyether ester and the like. These can be used alone or in combination of two or more.

  Examples of the antibacterial agents include zeolite antibacterial agents such as silver zeolite and silver-zinc zeolite, silica gel antibacterial agents such as complexed silver-silica gel, glass antibacterial agents, calcium phosphate antibacterial agents, and zirconium phosphate antibacterial agents. Silicate antibacterial agents such as silver-magnesium aluminate, titanium oxide antibacterial agents, ceramic antibacterial agents, whisker antibacterial agents, etc .; formaldehyde releasing agents, halogenated aromatic compounds, road Organic antibacterial agents such as propargyl derivatives, thiocyanato compounds, isothiazolinone derivatives, trihalomethylthio compounds, quaternary ammonium salts, biguanide compounds, aldehydes, phenols, pyridine oxide, carbanilide, diphenyl ether, carboxylic acid, organometallic compounds; inorganic and organic Hybrid antibacterial agent; natural anti Agent, and the like. These can be used alone or in combination of two or more.

  Examples of the colorant include organic dyes, inorganic pigments, and organic pigments. These can be used alone or in combination of two or more.

  It does not specifically limit as a manufacturing method of the thermoplastic resin composition of this invention. For example, it can be produced by drying the above-described components, additives and the like and then melt-kneading them in a melt-kneader such as a single-screw or twin-screw extruder. The kneading temperature is selected for the type of the thermoplastic resin (A). Moreover, when a compounding component is a liquid, it can also manufacture by adding to a melt-kneader on the way using a liquid supply pump etc.

  The molding method of the heat conductive molded body of the present invention is not particularly limited, and is injection molding, extrusion molding (sheet extrusion, profile extrusion), two-color molding, hollow molding, compression molding, vacuum molding, foam molding, blow molding, transfer. Although a molded product can be obtained by a known molding method such as molding, injection molding, extrusion molding, and transfer molding are preferable from the viewpoint of easy moldability.

  Next, although the manufacture example, an Example, and a comparative example are given and demonstrated further in detail about the heat conductive resin of this invention, this invention is not restrict | limited only to this Example.

The raw material components used for preparing the resin composition are shown below.
Thermoplastic resin (A):
Polyethylene terephthalate (A-1): Novapex (trade name) PBKII (trade name) manufactured by Mitsubishi Chemical Corporation, number average molecular weight 28,000
Polyethylene terephthalate (A-2): GS-100 (trade name) manufactured by Mitsubishi Chemical Corporation, number average molecular weight 22,500
Polyethylene terephthalate (A-3) KS710B-8S (trade name) manufactured by Kuraray Co., Ltd., number average molecular weight 61,000
Polyester-polyether copolymer (A-4):
As the polyester-polyether copolymer, one produced by the following method was used.
That is, in a reactor equipped with a stirrer and a gas discharge outlet, 70 parts by weight of polyethylene terephthalate (PET) (IV = 0.65) having an antimony metal concentration of 200 ppm by weight produced with an antimony catalyst, PET and polyether 0.2 parts by weight of antimony trioxide of 160 ppm with respect to the antioxidant, and 0.2 parts by weight of an antioxidant (Irganox (trade name) 1010 manufactured by Ciba Specialty Chemicals), 30 parts by weight of polyether which is bisol 18EN described below After the preparation, the mixture was kept at 270 ° C. for 2 hours, then depressurized with a vacuum pump, and after 1 torr and keeping for 3 hours, the polyester-polyether copolymer was obtained. The number average molecular weight of the obtained polyester-polyether copolymer was 25,400.

The bisol 18EN has a number average (m + n) of 18 in the structure of the general formula (2).
Polybutylene terephthalate (A-5): Mitsubishi Engineer Plastics 5008L (trade name), number average molecular weight 19,000
Nylon 6 (A-6): Unitika A1015N (trade name)
Polyphenylene sulfide (A-7): FZ-2100 (trade name) manufactured by Dainippon Ink & Chemicals, Inc.
Graphite (B):
Scale-like graphite (B-1): CPB-80 (trade name) manufactured by Chuetsu Graphite Industries Co., Ltd., volume average particle diameter 300 μm, fixed carbon content 99.9%, aspect ratio 100
Scale-like graphite (B-2): BF-40AK (trade name) manufactured by Chuetsu Graphite Industries Co., Ltd., volume average particle diameter 50 μm, fixed carbon amount 99.9%, aspect ratio 30
Scale-like graphite (B-3): MD-100C (trade name) manufactured by Chuetsu Graphite Industries Co., Ltd., volume average particle diameter 170 μm, fixed carbon amount 93.6%, aspect ratio 80
Spherical graphite (B-4): WF-15C (trade name) manufactured by Chuetsu Graphite Industries Co., Ltd., volume average particle diameter 16 μm, fixed carbon content 99.9%, aspect ratio 1
Reinforcing agent (C):
Glass fiber: T187H / PL (trade name) manufactured by Nippon Electric Glass Co., Ltd., single body thermal conductivity 1.0 W / (m · K), fiber diameter 13 μm, number average fiber length 3.0 mm
Flame retardant (D)
Brobe flame retardant SAYTEX7010P (trade name) manufactured by Albemarle
Flame retardant aid (E)
Nippon Seiko Co., Ltd. Antimony trioxide PATOX-P (trade name)

[Evaluation method]
Number average molecular weight: A sample was prepared by dissolving the thermoplastic resin used in the present invention in a mixed solvent of p-chlorophenol (manufactured by Tokyo Chemical Industry Co., Ltd.) and toluene in a volume ratio of 3: 8 to a concentration of 0.25% by weight. . The standard material was polystyrene, and a similar sample solution was prepared. The measurement was performed using a high temperature GPC (350 HT-GPC System manufactured by Viscotek) under conditions of a column temperature of 80 ° C. and a flow rate of 1.00 mL / min. A differential refractometer (RI) was used as a detector.

  Extrusion kneading temperature: The heat conductive resin composition is prepared by extrusion melt kneading. The extrusion kneading temperature at that time varies depending on the thermoplastic resin (A), and extrusion kneading was performed at the extrusion barrel temperature shown in Table 1. .

  Molding processing conditions: The molding processing temperature of the molded body used for evaluation was different depending on the thermoplastic resin (A), and injection molding was performed at the molding processing temperature shown in Table 1. Moreover, it shape | molded by fixing to injection speed 150mm / s and injection pressure 150MPa.

  Graphite volume average particle size: Using a microtrack particle size distribution measuring device (MICROTRAC MT3300EXII, manufactured by Nikkiso Co., Ltd.), graphite particles were put into an aqueous solvent, and then subjected to ultrasonic vibration for 60 seconds, followed by measurement. The volume average particle diameter of the graphite particles after molding was measured after firing a molded body having a diameter of 26 mm × 1 mm at 620 ° C. for 1 hour, and then extracting only the graphite particles contained in the molded body.

  Aspect ratio of graphite: Using a scanning electron microscope (SEM) (JSM-6060LA manufactured by JEOL Ltd.), the average ratio of the longest diameter and the shortest diameter of 100 graphite particles was calculated. About the aspect-ratio of the graphite particle after shaping | molding processing, it computed by the same method using the molded object of (phi) 26 mm x 1 mm thickness.

  Thermal conductivity: Using the obtained pellets of the thermally conductive resin composition, a φ26 mm × 1 mm thickness was prepared with an injection molding machine [Toyo Machine Metal Co., Ltd., Si-15IV], and conformed to ASTM E1461 standard. In conformity, the thermal conductivity in the plane direction and the thickness direction in the air at room temperature was measured with a laser flash method thermal conductivity measuring device (LFA447 manufactured by NETZSCH). Specific gravity: The specific gravity was measured by an underwater substitution method in accordance with the ISO 1183 standard using a molded body having a diameter of φ26 mm × 1 mm.

Flowability (spiral flow): The pellets of the obtained heat conductive resin composition are molded in accordance with the thermoplastic resin using an injection molding machine [Toyo Machine Metal Co., Ltd., Si-30IV]. The flow length in a spiral shaped body (10 mm width × 1 mm thickness, pitch 5 mm) was measured at an injection pressure of 150 MPa and an injection speed of 150 mm / s at the temperature and mold temperature.
Heat resistance: HDT (high load)
A test piece having a thickness of 80 mm × 40 mm × 4 mm was prepared with an injection molding machine [Toyo Machine Metal Co., Ltd., Si-30IV] and measured in accordance with ISO75 standard.
Flammability: Performed in accordance with the rules of UL94 standard shown below. The upper end of the test piece is clamped to fix the test piece vertically, a predetermined flame is applied to the lower end for 10 seconds, and the burning time (first time) of the test piece is measured. Immediately after extinguishing the fire, flame is again applied to the lower end, and the burning time (second time) of the test piece is measured. The same measurement is repeated for five pieces, and a total of 10 data items are obtained, including five pieces of data for the first burning time and five pieces of data for the second burning time. The total of 10 data is T, and the maximum value of 10 data is M. If T is 50 seconds or less, M is 10 seconds or less and does not burn up to the clamp, and if the flamed melt falls and does not ignite cotton 12 inches below, it is equivalent to V-0, T is 250 seconds or less If M is 30 seconds or less and the other conditions satisfy the same conditions as V-0, the result is equivalent to V-1.

[Examples 1-7]
The thermoplastic resins (A-1) to (A-5) were dried at 140 ° C. for 4 hours using a hot air dryer, and mixed so that the weight ratios shown in Table 2 were obtained. To this, 0.3 parts by weight of a phenol-based stabilizer (AO-60 manufactured by ADEKA Corporation) and a phosphorus-based antioxidant (ADEKA STAB (trade name) PEP-36 manufactured by ADEKA Co., Ltd.) with respect to 100 parts by weight of the resin. added. Using this mixture, Technobel Co., Ltd. 25 mm co-rotating fully meshed twin screw extruder MFU25TW-60HG-NH-1300, discharge rate 20 kg / h, screw rotation speed 150 rpm, extrusion barrel temperature shown in Table 1 The resin composition pellets were obtained by melt-kneading with setting.
Molded bodies were prepared from the obtained resin composition pellets by injection molding, and various evaluations were made. Table 2 shows the volume average particle diameter and aspect ratio of graphite particles contained in the molded body, and various physical property values.

[Example 8]
The thermoplastic resin was changed to (A-6), dried at 120 ° C. for 6 hours using a hot air drier, and mixed so that the weight ratio shown in Table 2 was obtained. Example 1 was repeated except that the extrusion barrel temperature and the injection molding conditions were changed. Table 2 shows the volume average particle diameter and aspect ratio of graphite particles contained in the molded body, and various physical property values.

[Example 9]
The thermoplastic resin was changed to (A-7), dried at 140 ° C. for 4 hours using a hot air drier, and mixed so that the weight ratio shown in Table 2 was obtained. Example 1 was repeated except that the extrusion barrel temperature and the injection molding conditions were changed. Table 2 shows the volume average particle diameter and aspect ratio of graphite particles contained in the molded body, and various physical property values.

[Comparative Examples 1-5]
Example 1 was repeated except that the formulation was changed to the formulation shown in Table 3. Table 3 shows the volume average particle diameter and aspect ratio of the graphite particles contained in the compact and various physical property values.

[Comparative Example 6]
Example 8 was repeated except that the formulation shown in Table 3 was changed. Table 3 shows the volume average particle diameter and aspect ratio of the graphite particles contained in the compact and various physical property values.

  When the Examples and Comparative Examples were compared and the same amount of graphite was contained, the volume average particle diameter, fixed carbon amount, and aspect ratio of the graphite used in the Examples were the graphite of the present invention, and thus the thermal conductivity. It can be seen that the value of spiral flow (formability) is high. By using graphite with a volume average particle diameter of graphite before melt kneading, which is a large particle diameter of 201 μm or more, the graphite particle diameter contained in the resin composition after molding is kept high after melt kneading, It can be said that the thermal conductivity, particularly the spiral flow, can be greatly improved. Moreover, as shown in Examples 1-9, it turns out that this invention expresses the effect of this invention irrespective of the kind and compounding ratio of a thermoplastic resin.

  Since the heat conductive resin composition of the present invention has excellent heat conductivity, molding processability, and low specific gravity, it can be used for applications in which heat generation is a problem, and furthermore, a metal having high heat conductivity, etc. By substituting, a molded body can be obtained easily and inexpensively with high weight reduction and a high degree of freedom in shape. In addition, the heat conductive resin composition of the present invention is excellent in electromagnetic shielding properties and is suitable for applications requiring electromagnetic shielding properties, such as a heat radiating case, a heat radiating chassis, lighting, and a lamp heat sink for automobiles. Suitable for various applications.

DESCRIPTION OF SYMBOLS 1 Camera housing thermal housing 2 Box-shaped thermal housing 3, 4 LED lamp housing heat sink 5 Heat sink 10 First cylinder 11 Second cylinder 12 First radiation fin 13 Second radiation fin 14 Opening 15 Body 16 17 Radiation fin 18 Support plate 19 Frame 20 Radiation fin 21a, 21b Rib 22 Support plate 23 Recess 24a, 24b Protrusion 25 Plate-shaped radiation fin

Claims (9)

(A) The thermoplastic resin is 30 to 90% by mass in the whole thermally conductive resin composition , (B) the volume average particle diameter in the molded body is 40 to 700 μm, the fixed carbon amount is 98% by mass or more, and the aspect ratio is 21. The scaly graphite as described above contains at least 10 to 70% by mass of the entire thermally conductive resin composition , has a specific gravity of 1.4 to 2.0, and has a thermal conductivity of 1 W / (m · and the K) or more, the (A) thermoplastic resins may be a polyester resin, a polyamide resin, and one or more selected from the group consisting of polyphenylene sulfide resin, wherein the polyester resin is polybutylene terephthalate, polyethylene terephthalate, And a polyester-polyether copolymer, one or more kinds selected from the group consisting of: a heat conductive resin composition. The said (A) thermoplastic resin contains 30-70 mass% in the whole heat conductive resin composition, and the said (B) scaly graphite contains 70-30 mass% in the whole heat conductive resin composition. 2. The heat conductive resin composition according to 1.   The thermally conductive resin composition is a melt-kneaded product, and the flake graphite (B) before melt-kneading has a volume average particle diameter of 201 to 700 μm, a fixed carbon amount of 98 mass% or more, and an aspect ratio of 21 or more. The thermally conductive resin composition according to claim 1, wherein the thermally conductive resin composition is provided.   The heat according to any one of claims 1 to 3, wherein the number average molecular weight of the polybutylene terephthalate, polyethylene terephthalate, and polyester-polyether copolymer is 12,000 to 70,000. Conductive resin composition.   The said polyamide resin is 1 or more types chosen from the group which consists of nylon 6, nylon 6,6, nylon 4,6, and nylon 12, The any one of Claims 1-4 characterized by the above-mentioned. Thermally conductive resin composition.   The heat conductive resin composition according to any one of claims 1 to 5, wherein the scaly graphite (B) is natural graphite.   It is comprised with the heat conductive resin composition as described in any one of Claims 1-6, The heat dissipation housing | casing characterized by the above-mentioned.   It is comprised with the heat conductive resin composition as described in any one of Claims 1-6, The thermal radiation chassis characterized by the above-mentioned.   An automotive LED lamp heat sink comprising the thermally conductive resin composition according to any one of claims 1 to 6.

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