Patent Application
20190136004
The present invention relates to a heat conductive foam sheet for electronic equipment and a heat conductive laminate for electronic equipment for effectively dissipating interior heat of electronic equipment to the exterior.
In electronic equipment such as smartphones requiring a reduction in size, electronic parts are highly densely integrated and generate a large amount of heat. Since such heat causes a malfunction, a heat sink material is provided for dissipating the heat to the exterior of the equipment. As the heat sink material, which is generally provided between electronic parts serving as a heat generator and a metal case, e.g., heat dissipation grease and heat dissipation gel, which highly accurately follows a concavo-convex shape and urethane foam impregnated with each of these are used (for example, Patent Literature 1).
PTL1: Japanese Patent Laid-Open No. 2003-31980
The heat dissipation grease satisfactorily dissipates heat; however, it has a problem in that once it is applied, it is difficult to re-apply the grease, with the result that the production yield decreases. On the other hand, the heat dissipation gel has a problem in that it is generally difficult to process the gel into a sheet-like product having a thickness of 1 mm or less, and that, if compressed, the shape is deformed. In addition, the heat-dissipation gel has a problem in that if the thickness of the sheet reduces, compressive strength increases and flexibility decreases.
In contrast, it is difficult to mold a urethane foam into a sheet having a thickness of 1 mm or less for the reason of its process, and it is difficult to increase a ratio for a thin sheet-like product. Thus, the urethane foam has a problem in that the compressive strength increases and flexibility disappears.
The present invention was made in view of the above problems of conventional products and is directed to providing a heat conductive foam sheet for electronic equipment and a heat conductive laminate for electronic equipment sufficiently thin and flexible to be suitably used in the interior of electronic equipment and excellent in heat conductivity.
The present invention mainly relates to the following [1] to [3].
[1] A heat conductive foam sheet for electronic equipment containing a heat conductor in an elastomer resin portion constituting the foam sheet, in which the content of the heat conductor relative to 100 parts by mass of the elastomer resin is 100 to 500 parts by mass, the 25% compressive strength of the foam sheet is 200 kPa or less and a thickness thereof is 0.05 to 1 mm.
[2] A heat conductive foam sheet for electronic equipment containing a heat conductor in an elastomer resin portion constituting the foam sheet, in which the heat conductor has a scale-like shape defined by a major axis of 1 to 300 μm, a minor axis of 1 to 300 μm and a ratio of the major axis to thickness (major axis/thickness) of 2 to 500 and/or a fibrous shape defined by a diameter of 0.01 to 50 μm and a ratio of length to the diameter (length/diameter) of 5 to 30,000; and the 25% compressive strength of the foam sheet is 200 kPa or less and the thickness thereof is 0.05 to 1 mm.
[3] A heat conductive laminate for electronic equipment, which has a heat conductive sheet having a heat conductivity of 200 W/m·K or more, on at least one of the surfaces of a foam sheet having a 25% compressive strength of 200 kPa or less and a thickness of 0.05 to 1.0 mm; and which has a thickness of 0.08 to 1.50 mm.
According to the present invention, it is possible to provide a heat conductive foam sheet for electronic equipment and a heat conductive laminate for electronic equipment sufficiently thin and flexible to be suitably used in the interior of electronic equipment and excellent in heat conductivity.
The heat conductive foam sheet (1) for electronic equipment of the present invention refers to a heat conductive foam sheet for electronic equipment containing a heat conductor in an elastomer resin portion constituting the foam sheet, in which the content of the heat conductor relative to 100 parts by mass of the elastomer resin is 100 to 500 parts by mass, the 25% compressive strength of the foam sheet is 200 kPa or less and the thickness thereof is 0.05 to 1 mm.
<Foam Sheet>
In the heat conductive foam sheet (1) for electronic equipment, the 25% compressive strength of the foam sheet is 200 kPa or less. It is not preferable that the compressive strength exceeds 200 kPa, because, if so, the flexibility of the foam sheet decreases. In view of the flexibility of the foam sheet, the 25% compressive strength of the foam sheet is preferably 5 kPa or more, more preferably 50 kPa or more and further preferably 55 kPa or more; and preferably 190 kPa or less, more preferably 180 kPa or less, further preferably 150 kPa or less and further more preferably 100 kPa or less.
As a specific numerical value, the 25% compressive strength of the foam sheet is preferably 5 to 190 kPa, more preferably 50 to 190 kPa, more preferably 50 to 150 kPa and further preferably 55 to 100 kPa.
The foam sheet to be used in the heat conductive foam sheet (1) for electronic equipment is preferably constituted of an elastomer resin containing a liquid elastomer in an amount of 10 mass % or more. The 50% compressive strength of the foam sheet is preferably 200 kPa or less. If the 50% compressive strength of the foam sheet is 200 kPa or less, the foam sheet can be suitably used in thin electronic equipment such as mobile terminals.
In view of flexibility improvement, the 50% compressive strength of the foam sheet is more preferably 150 kPa or less and further preferably 100 kPa or less.
The content of the liquid elastomer in the elastomer resin is preferably 10 mass % or more and more preferably 20 mass % or more; and preferably 90 mass % or less and more preferably 80 mass % or less.
The thickness of the foam sheet is 0.05 to 1 mm. If the thickness of the foam sheet is less than 0.05 mm, the foam sheet is easily torn; whereas, if the thickness exceeds 1 mm, it is difficult to use the foam sheet in the interior space of small electronic equipment. In view of the strength of the foam sheet, the thickness of the foam sheet is preferably 0.05 to 0.8 mm, more preferably 0.05 to 0.7 mm and further preferably 0.05 to 0.5 mm.
The dielectric constant of the foam sheet is preferably 4 or less. It is not preferable that the dielectric constant of the foam sheet exceeds 4, because, if so, malfunction of electronic equipment is sometimes caused. The dielectric constant of the foam sheet is preferably 1 to 3 and more preferably 1 to 2.
The heat conductivity of the foam sheet is preferably 0.3 to 10 W/m·K and more preferably 0.4 to 2.0 W/m·K. If the heat conductivity of the foam sheet falls within the above range, it is possible to effectively dissipate interior heat of electronic equipment to the exterior.
The expansion ratio of the foam sheet is preferably 1.5 to 5, more preferably 1.5 to 3 and further preferably 1.5 to 2.5. If the expansion ratio of the foam sheet falls within the above range, it is possible for the foam sheet to be not only thin but also flexible.
The apparent density of the foam sheet is preferably 0.4 g/cm3 or more, more preferably 0.5 g/cm3 or more, more preferably 0.6 g/cm3 or more, further preferably 0.7 g/cm3 or more and further more preferably 0.85 g/cm3 or more; and preferably 1.5 g/cm3 or less, more preferably 1.4 g/cm3 or less and further preferably 1.2 g/cm3 or less.
As a more specific numerical value, the apparent density of the foam sheet is preferably 0.4 to 1.5 g/cm3, more preferably 0.4 to 1.4 g/cm3, further preferably 0.7 to 1.4 g/cm3 and further more preferably 0.85 to 1.2 g/cm3. If the apparent density of the foam sheet falls within the above range, it is possible for the foam sheet to obtain a desired thickness in combination with flexibility and heat conductivity.
<Elastomer Resin>
Examples of the elastomer resin that can be used in the heat conductive foam sheet (1) for electronic equipment include an acrylonitrile butadiene rubber, a liquid-state acrylonitrile butadiene rubber, an ethylene-propylene-diene rubber, a liquid-state ethylene-propylene-diene rubber, an ethylene-propylene rubber, a liquid-state ethylene-propylene rubber, a natural rubber, a liquid-state natural rubber, a polybutadiene rubber, a liquid-state polybutadiene rubber, a polyisoprene rubber, a liquid-state polyisoprene rubber, a styrene-butadiene block copolymer, a liquid-state styrene-butadiene block copolymer, a hydrogenated styrene-butadiene block copolymer, a liquid-state hydrogenated styrene-butadiene block copolymer, a hydrogenated styrene-butadiene-styrene block copolymer, a liquid-state hydrogenated styrene-butadiene-styrene block copolymer, a hydrogenated styrene-isoprene block copolymer, a liquid-state hydrogenated styrene-isoprene block copolymer, a hydrogenated styrene-isoprene-styrene block copolymer and a liquid-state hydrogenated styrene-isoprene-styrene block copolymer. Of these, an acrylonitrile butadiene rubber, a liquid-state acrylonitrile butadiene rubber, an ethylene-propylene-diene rubber, a liquid-state ethylene-propylene-diene rubber and a butyl rubber (isobutylene-isoprene rubber) are preferable.
<Heat Conductor>
Examples of the heat conductor that can be used in the heat conductive foam sheet (1) for electronic equipment include aluminum oxide, magnesium oxide, boron nitride, talc, aluminum nitride, graphite and graphene. Of these, aluminum oxide and magnesium oxide are preferable. These heat conductors may be used alone or as a mixture of two or more.
The heat conductivity of the heat conductor is preferably 5 W/m·K or more, and more preferably 20 W/m·K or more. If the heat conductivity falls within the above range, the heat conductivity of the resultant foam sheet will be sufficiently high.
The content of the heat conductor relative to 100 parts by mass of the elastomer resin is 100 to 500 parts by mass. If the content of the heat conductor is less than 100 parts by mass, it is impossible for the foam sheet to obtain sufficient heat conductivity; whereas, if the content of the heat conductor exceeds 500 parts by mass, the flexibility of the foam sheet decreases. In view of heat conductivity and flexibility of the foam sheet, the content of the heat conductor relative to 100 parts by mass of the elastomer resin is preferably 120 to 480 parts by mass, more preferably 120 to 400 parts by mass, further preferably 150 to 450 parts by mass and further more preferably 150 to 350 parts by mass.
<Optional Components>
In the heat conductive foam sheet (1) for electronic equipment, if necessary, various types of additional components can be contained within the range where the objects of the present invention will not be damaged.
The types of additional components are not particularly limited and various additives that are usually used in expansion molding can be used. Examples of such additives include a lubricant, a shrinkage inhibitor, a foam nucleating agent, a nucleating agent for crystallization, a plasticizer, a coloring agent (e.g., pigment, dye), a UV absorbent, an antioxidant, an anti-aging agent, a filler excluding the aforementioned conductivity imparting material, a strengthening agent, a flame retardant, a flame retardant promoter, an antistatic agent, a surfactant, a vulcanizing agent and a surface treatment agent. The addition amounts of additives can be appropriately selected as long as formation of air foam is not damaged. The addition amounts of additives that are usually used for expansion and molding of a resin can be employed. These additives can be used alone or in combination of two or more.
The lubricant not only improves flowability of a resin but also suppresses deterioration of a resin by heat. The lubricant to be used in the present invention is not particularly limited as long as it effectively improves flowability of a resin. Example thereof include hydrocarbon lubricants such as liquid paraffin, paraffin wax, microwax and polyethylene wax; fatty acid lubricants such as stearic acid, behenic acid and 12-hydroxy stearic acid; and ester lubricants such as butyl stearate, stearic acid monoglyceride, pentaerythritol tetrastearate, hydrogenated castor oil and stearyl stearate.
The addition amount of the lubricant relative to 100 parts by mass of a resin is preferably about 0.01 to 5 parts by mass, more preferably 0.05 to 4 parts by mass and further preferably 0.1 to 3 parts by mass. If the addition amount exceeds 10 parts by mass, flowability becomes extremely high, with the result that the expansion ratio may decrease. In contrast, if the addition amount is less than 0.01 parts by mass, flowability cannot be improved and stretchability during foam formation decreases, with the result that the expansion ratio may decrease.
Examples of the flame retardant include, other than metal hydroxides such as aluminum hydroxide and magnesium hydroxide, bromine-based flame retardants such as decabromodiphenyl ether and phosphorus-based flame retardants such as ammonium polyphosphate.
Examples of the flame retardant promoter include antimony compounds such as antimony trioxide, antimony tetraoxide, antimony pentoxide, sodium pyroantimonate, antimony trichloride, antimony trisulfide, antimony oxychloride, antimony dichloride perchloropentane and potassium antimonate; boron compounds such as zinc metaborate, zinc tetraborate, zinc borate and basic zinc borate; zirconium oxides; tin oxides; and molybdenum oxides.
<Method for Producing Foam Sheet>
The heat conductive foam sheet (1) for electronic equipment of the present invention can be produced by a chemical foaming method or a physical foaming method known in the art. The method for producing the sheet is not particularly limited.
Note that, as a foam-processing method, methods known in the art including those described in Plastic Foam Handbook (edited by Hiroshi Maki and Atsushi Osakada, published by NIKKAN KOGYO SHIMBUN, LTD., 1973) can be used.
The heat conductive foam sheet (2) for electronic equipment of the present invention refers to a heat conductive foam sheet for electronic equipment containing a heat conductor in an elastomer resin portion constituting the foam sheet, in which the heat conductor has a scale-like shape defined by a major axis of 1 to 300 μm, a minor axis of 1 to 300 μm, a ratio of the major axis to thickness (major axis/thickness) of 2 to 500 and/or a fibrous shape defined by a diameter of 0.01 to 50 μm, a ratio of length to diameter (length/diameter) of 5 to 30,000, the 25% compressive strength of the foam sheet is 200 kPa or less and the thickness thereof is 0.05 to 1 mm.
<Foam Sheet>
In the heat conductive foam sheet (2) for electronic equipment, the 25% compressive strength of the foam sheet to be used herein is 200 kPa or less. It is not preferable that the compressive strength exceeds 200 kPa, because, if so, the flexibility of the foam sheet decreases. In view of the flexibility of the foam sheet, the 25% compressive strength of the foam sheet is preferably 5 kPa or more, more preferably 50 kPa or more and further preferably 55 kPa or more; and preferably 190 kPa or less, more preferably 180 kPa or less, further preferably 150 kPa or less and further more preferably 100 kPa or less.
As a specific numerical value, the 25% compressive strength of the foam sheet is preferably 5 to 190 kPa, more preferably 50 to 190 kPa, further preferably 50 to 150 kPa and further more preferably 55 to 100 kPa.
The foam sheet to be used in the heat conductive foam sheet (2) for electronic equipment is preferably constituted of an elastomer resin containing a liquid elastomer in an amount of 10 mass % or more. The 50% compressive strength of the foam sheet is preferably 200 kPa or less. If the 50% compressive strength of the foam sheet is 200 kPa or less, the foam sheet can be suitably used in thin electronic equipment such as mobile terminals.
In view of flexibility improvement, the 50% compressive strength of the foam sheet is more preferably 150 kPa or less and further preferably 100 kPa or less.
The content of the liquid elastomer in the elastomer resin is preferably 10 mass % or more and more preferably 20 mass % or more; and preferably 90 mass % or less and more preferably 80 mass % or less.
The thickness of the foam sheet is 0.05 to 1 mm. If the thickness of the foam sheet is less than 0.05 mm, the foam sheet is easily torn; whereas, if the thickness exceeds 1 mm, it is difficult to use the foam sheet in the interior space of small electronic equipment. In view of the strength of the foam-sheet, the thickness of the foam sheet is preferably 0.05 to 0.8 mm, more preferably 0.05 to 0.7 mm and further preferably 0.05 to 0.5 mm.
The heat conductivity of the foam sheet is preferably 0.3 to 10 W/m·K and more preferably 0.4 to 2 W/m·K. If the heat conductivity of the foam sheet falls within the above range, it is possible to effectively dissipate interior heat of electronic equipment to the exterior.
The expansion ratio of the foam sheet is preferably 1.5 to 5, more preferably 1.5 to 3 and further preferably 1.5 to 2.5. If the expansion ratio of the foam sheet falls within the above range, it is possible to obtain a foam sheet not only thin but also flexible.
The apparent density of the foam sheet is preferably 0.4 g/cm3 or more, more preferably 0.5 g/cm3 or more, more preferably 0.6 g/cm3 or more, further preferably 0.7 g/cm3 or more and further more preferably 0.85 g/cm3 or more; and preferably 1.5 g/cm3 or less, more preferably 1.4 g/cm3 or less and further preferably 1.2 g/cm3 or less.
As a specific numerical value, the apparent density of the foam sheet is preferably 0.4 to 1.5 g/cm3, more preferably 0.4 to 1.4 g/cm3, further preferably 0.7 to 1.4 g/cm3, and further more preferably 0.85 to 1.2 g/cm3. If the apparent density of the foam sheet falls within the above range, it is possible to obtain a foam sheet having a desired thickness in combination with flexibility and heat conductivity.
<Heat Conductor>
In the heat conductive foam sheet (2) for electronic equipment, a heat conductor, which has a scale-like shape defined by a major axis of 1 to 300 μm, a minor axis of 1 to 300 μm, a ratio of the major axis to thickness (major axis/thickness) of 2 to 500 and/or a fibrous shape defined by a diameter of 0.01 to 50 μm, a ratio of length to the diameter (length/diameter) of 5 to 30,000, is used. If the shape is defined by numerical values outside the above range, it is impossible to highly densely pack the foam sheet with the heat conductor, with the result that the heat conductivity of the foam sheet decreases.
In the case where the heat conductor has a scale-like shape, the major axis is preferably 1 to 250 μm, more preferably 2 to 200 μm and further preferably 2 to 50 μm. The minor axis is preferably 1 to 250 μm, more preferably 2 to 200 μm and further preferably 2 to 50 μm. The ratio of major axis to thickness (major axis/thickness) is preferably 2.5 to 450 and more preferably 3 to 400.
In the case where the heat conductor has a fibrous shape, the diameter is more preferably 0.05 to 45 μm and further preferably 0.07 to 40 μm. The ratio of length to diameter (length/diameter) is more preferably 6 to 28,000 and further preferably 7 to 26,000.
Examples of the heat conductor include boron nitride, talc, aluminum nitride, a carbon nanotube, a carbon fiber, aluminum oxide, magnesium oxide, graphite and graphene. Of these, boron nitride, talc, aluminum nitride, graphite, a carbon nanotube and a carbon fiber are preferable. These heat conductors may be used alone or as a mixture of two or more.
The heat conductivity of the heat conductor is preferably 30 W/m·K or more and more preferably 40 W/m·K or more. If the heat conductivity falls within the above range, the heat conductivity of the resultant foam sheet will be sufficiently high.
The content of the heat conductor relative to 100 parts by mass of the elastomer resin is preferably 100 to 500 parts by mass, preferably 120 to 400 parts by mass and more preferably 150 to 350 parts by mass. If the content of the heat conductor falls within the above range, it is possible for the foam sheet to obtain sufficient heat conductivity while suppressing reduction of flexibility.
<Elastomer Resin>
Examples of the elastomer resin that can be used in the heat conductive foam sheet (2) for electronic equipment include an acrylonitrile butadiene rubber, a liquid-state acrylonitrile butadiene rubber, an ethylene-propylene-diene rubber, a liquid-state ethylene-propylene-diene rubber, an ethylene-propylene rubber, a liquid-state ethylene-propylene rubber, a natural rubber, a liquid-state natural rubber, a polybutadiene rubber, a liquid-state polybutadiene rubber, a polyisoprene rubber, a liquid-state polyisoprene rubber, a styrene-butadiene block copolymer, a liquid-state styrene-butadiene block copolymer, a hydrogenated styrene-butadiene block copolymer, a liquid-state hydrogenated styrene-butadiene block copolymer, a hydrogenated styrene-butadiene-styrene block copolymer, a liquid-state hydrogenated styrene-butadiene-styrene block copolymer, a hydrogenated styrene-isoprene block copolymer, a liquid-state hydrogenated styrene-isoprene block copolymer, a hydrogenated styrene-isoprene-styrene block copolymer and a liquid-state hydrogenated styrene-isoprene-styrene block copolymer. Of these, an acrylonitrile butadiene rubber, a liquid-state acrylonitrile butadiene rubber, an ethylene-propylene-diene rubber and a liquid-state ethylene-propylene-diene rubber are preferable.
<Optional Components>
In the heat conductive foam sheet (2) for electronic equipment, if necessary, various types of additional components can be contained within the range where the objects of the present invention will not be damaged.
The types of additional components are not particularly limited and various additives that are usually used in expansion molding can be used. Examples of such additives include a lubricant, a shrinkage inhibitor, a foam nucleating agent, a nucleating agent for crystallization, a plasticizer, a coloring agent (e.g., pigment, dye), a UV absorbent, an antioxidant, an anti-aging agent, a filler excluding the aforementioned conductivity imparting material, a strengthening agent, a flame retardant, a flame retardant promoter, an antistatic agent, a surfactant, a vulcanizing agent and a surface treatment agent. The addition amounts of additives can be appropriately selected as long as formation of air foam is not damaged. The addition amounts of additives that are usually used for expansion molding of a resin can be employed. These additives can be used alone or in combination of two or more.
The lubricant not only improves flowability of a resin but also suppresses deterioration of a resin by heat. The lubricant to be used in the present invention is not particularly limited as long as it effectively improves flowability of a resin. Example thereof include hydrocarbon lubricants such as liquid paraffin, paraffin wax, microwax and polyethylene wax; fatty acid lubricants such as stearic acid, behenic acid and 12-hydroxy stearic acid; and ester lubricants such as butyl stearate, stearic acid monoglyceride, pentaerythritol tetrastearate, hydrogenated castor oil and stearyl stearate.
The addition amount of lubricant relative to 100 parts by mass of a resin is preferably about 0.01 to 5 parts by mass, more preferably 0.05 to 4 parts by mass and further preferably 0.1 to 3 parts by mass. If the addition amount exceeds 5 parts by mass, flowability becomes extremely high, with the result that the expansion ratio may decrease. In contrast, if the addition amount is less than 0.01 parts by mass, flowability cannot be improved and stretchability during foam formation decreases, with the result that the expansion ratio may decrease.
Examples of the flame retardant include, other than metal hydroxides such as aluminum hydroxide and magnesium hydroxide, bromine-based flame retardants such as decabromodiphenyl ether and phosphorus-based flame retardants such as ammonium polyphosphate.
Examples of the flame retardant promoter include antimony compounds such as antimony trioxide, antimony tetroxide, antimony pentoxide, sodium pyroantimonate, antimony trichloride, antimony trisulfide, antimony oxychloride, antimony dichloride perchloropentane and potassium antimonate; boron compounds such as zinc metaborate, zinc tetraborate, zinc borate and basic zinc borate; zirconium oxides; tin oxides; and molybdenum oxides.
<Method for Producing Foam Sheet>
The heat conductive foam sheet (2) for electronic equipment of the present invention can be produced by a chemical foaming method or a physical foaming method known in the art. The method for producing the sheet is not particularly limited.
Note that, as a foam-processing method, methods known in the art including those described in Plastic Foam Handbook (edited by Hiroshi Maki and Atsushi Osakada, published by NIKKAN KOGYO SHIMBUN, LTD., 1973) can be used.
The heat conductive laminate for electronic equipment of the present invention refers to a laminate having a heat conductive sheet, which has a heat conductivity of 200 W/m·K or more, on at least one of the surfaces of a foam sheet having a 25% compressive strength of 200 kPa or less and a thickness of 0.05 to 1.0 mm; and having a thickness of 0.08 to 1.50 mm.
<Foam Sheet>
In the heat conductive laminate for electronic equipment of the present invention, the 25% compressive strength of the foam sheet used herein is 200 kPa or less. It is not preferable that the compressive strength exceeds 200 kPa, because, if so, the flexibility of the foam sheet decreases. In view of the flexibility of the foam sheet, the 25% compressive strength of the foam sheet is preferably 5 kPa or more, more preferably 50 kPa or more and further preferably 55 kPa or more; and preferably 190 kPa or less, more preferably 180 kPa or less, further preferably 150 kPa or less and further more preferably 100 kPa or less.
As a specific numerical value, the 25% compressive strength of the foam sheet is preferably 5 to 190 kPa, more preferably 50 to 190 kPa, further preferably 50 to 150 kPa and further more preferably 55 to 100 kPa.
The foam sheet to be used in the heat conductive laminate for electronic equipment of the present invention is preferably constituted of an elastomer resin containing a liquid elastomer in an amount of 10 mass % or more. The 50% compressive strength of the foam sheet is preferably 200 kPa or less. If the 50% compressive strength of the foam sheet is 200 kPa or less, the foam sheet can be suitably used in thin electronic equipment such as mobile terminals.
In view of flexibility improvement, the 50% compressive strength of the foam sheet is more preferably 150 kPa or less and further preferably 100 kPa or less.
The content of the liquid elastomer in the elastomer resin is preferably 10 mass % or more and more preferably 20 mass % or more; and preferably 90 mass % or less and more preferably 80 mass % or less.
The thickness of the foam sheet is 0.05 to 1 mm. If the thickness of the foam sheet is less than 0.05 mm, the foam sheet is easily torn; whereas, if the thickness exceeds 1 mm, it is difficult to use the foam sheet in the interior space of small electronic equipment. In view of the strength of the foam-sheet, the thickness of the foam sheet is preferably 0.05 to 0.8 mm, more preferably 0.05 to 0.7 mm and further preferably 0.05 to 0.5 mm.
The heat conductivity of the foam sheet is preferably 0.01 to 10 W/m·K and more preferably 0.05 to 2 W/m·K. If the heat conductivity of the foam sheet falls within the above range, it is possible to effectively dissipate interior heat of electronic equipment to the exterior.
The expansion ratio of the foam sheet is preferably 1.5 to 6, more preferably 1.5 to 5.5. If the expansion ratio of the foam sheet falls within the above range, it is possible for the foam sheet to be not only thin but also flexible.
The apparent density of the foam sheet is preferably about 0.1 to 1.5 g/cm3, and preferably about 0.15 to 1.2 g/cm3.
<Heat Conductive Sheet>
The heat conductive laminate for electronic equipment of the present invention has a heat conductive sheet having a heat conductivity of 200 W/m·K or more, on at least one of the surfaces of a foam sheet. Owing to the heat conductive sheet provided, it is possible to further effectively dissipate interior heat of electronic equipment to the exterior. In order to effectively dissipate heat to the exterior, the heat conductivity of the heat conductive sheet is preferably 300 to 3,000 W/m·K and more preferably 300 to 2,000 W/m·K.
The heat conductive sheet is not particularly limited as long as the heat conductivity of the sheet satisfies the aforementioned heat conductivity range. Specifically, e.g., copper, aluminum, gold, silver, iron, graphite and graphene are preferable.
The heat conductive sheet preferably has a thickness of 3 to 500 μm and more preferably 20 to 170 μm, in order to use the sheet in the interior of precision equipment.
<Laminate>
The thickness of the laminate of the present invention is 0.08 to 1.50 mm. If the thickness of the laminate is less than 0.08 mm, the laminate is easily torn; whereas, if the thickness exceeds 1.50 mm, it is difficult to use the laminate in the interior space of small electronic equipment. The thickness of the laminate is preferably 0.1 to 1.25 mm and more preferably 0.2 to 0.95 mm.
<Elastomer Resin>
Examples of the elastomer resin that can be used in the heat conductive laminate for electronic equipment of the present invention include an acrylonitrile butadiene rubber, a liquid-state acrylonitrile butadiene rubber, a linear low-density polyethylene, an ethylene-propylene-diene rubber, a liquid-state ethylene-propylene-diene rubber, an ethylene-propylene rubber, a liquid-state ethylene-propylene rubber, a natural rubber, a liquid-state natural rubber, a polybutadiene rubber, a liquid-state polybutadiene rubber, a polyisoprene rubber, a liquid-state polyisoprene rubber, a styrene-butadiene block copolymer, a liquid-state styrene-butadiene block copolymer, a hydrogenated styrene-butadiene block copolymer, a liquid-state hydrogenated styrene-butadiene block copolymer, a hydrogenated styrene-butadiene-styrene block copolymer, a liquid-state hydrogenated styrene-butadiene-styrene block copolymer, a hydrogenated styrene-isoprene block copolymer, a liquid-state hydrogenated styrene-isoprene block copolymer, a hydrogenated styrene-isoprene-styrene block copolymer and a liquid-state hydrogenated styrene-isoprene-styrene block copolymer. Of these, an acrylonitrile butadiene rubber, a liquid-state acrylonitrile butadiene rubber, an ethylene-propylene-diene rubber, a liquid-state ethylene-propylene-diene rubber and a linear low-density polyethylene are preferable.
<Heat Conductive Filler>
In the heat conductive laminate for electronic equipment of the present invention, a heat conductive filler may be contained in the elastomer resin. Examples of the heat conductive filler include aluminum oxide, magnesium oxide, boron nitride, talc, aluminum nitride, graphite and graphene. Of these, aluminum oxide and magnesium oxide are preferable. These heat conductive fillers may be used alone or as a mixture of two or more.
The heat conductivity of the heat conductive filler is preferably 5 W/m·K or more and more preferably 20 W/m·K or more. If the heat conductivity falls within the above range, the heat conductivity of the resultant foam sheet will be sufficiently high.
The content of the heat conductive filler relative to 100 parts by mass of the elastomer resin is preferably 100 to 500 parts by mass, preferably 120 to 480 parts by mass and more preferably 150 to 450 parts by mass. If the content of the heat conductive filler falls within the above range, it is possible to obtain sufficient heat conductivity without reducing the flexibility of the foam sheet.
<Optional Component>
In the heat conductive laminate for electronic equipment of the present invention, if necessary, various types of additional components can be contained within the range where the objects of the present invention will not be damaged.
The types of additional components are not particularly limited and various additives that are usually used in expansion molding can be used. Examples of such additives include a lubricant, a shrinkage inhibitor, a foam nucleating agent, a nucleating agent for crystallization, a plasticizer, a coloring agent (e.g., pigment, dye), a UV absorbent, an antioxidant, an anti-aging agent, a filler excluding the aforementioned conductivity imparting material, a strengthening agent, a flame retardant, a flame retardant promoter, an antistatic agent, a surfactant, a vulcanizing agent and a surface treatment agent. The addition amounts of additives can be appropriately selected as long as formation of air foam is not damaged. The addition amounts of additives that are usually used for expansion and molding of a resin can be employed. These additives can be used alone or in combination of two or more.
The lubricant not only improves flowability of a resin but also suppresses deterioration of a resin by heat. The lubricant to be used in the present invention is not particularly limited as long as it effectively improves flowability of a resin. Example thereof include hydrocarbon lubricants such as liquid paraffin, paraffin wax, microwax and polyethylene wax; fatty acid lubricants such as stearic acid, behenic acid and 12-hydroxy stearic acid; and ester lubricants such as butyl stearate, stearic acid monoglyceride, pentaerythritol tetrastearate, hydrogenated castor oil and stearyl stearate.
The addition amount of lubricant relative to 100 parts by mass of a resin is preferably about 0.01 to 5 parts by mass, more preferably 0.05 to 3 parts by mass and further preferably 0.1 to 3 parts by mass. If the addition amount exceeds 5 parts by mass, flowability becomes extremely high, with the result that the expansion ratio may decrease. In contrast, if the addition amount is less than 0.01 parts by mass, flowability cannot be improved and stretchability during foam formation decreases, with the result that the expansion ratio may decrease.
Examples of the flame retardant include, other than metal hydroxides such as aluminum hydroxide and magnesium hydroxide, bromine-based flame retardants such as decabromodiphenyl ether and phosphorus-based flame retardants such as ammonium polyphosphate.
Examples of the flame retardant promoter include antimony compounds such as antimony trioxide, antimony tetraoxide, antimony pentoxide, sodium pyroantimonate, antimony trichloride, antimony trisulfide, antimony oxychloride, antimony dichloride perchloropentane and potassium antimonate; boron compounds such as zinc metaborate, zinc tetraborate, zinc borate and basic zinc borate; zirconium oxides; tin oxides; and molybdenum oxides.
<Method for Producing Foam Sheet>
The heat conductive laminate for electronic equipment of the present invention can be produced by a chemical foaming method or a physical foaming method known in the art. The production method is not particularly limited.
Note that, as a foam-processing method, methods known in the art including those described in Plastic Foam Handbook (edited by Hiroshi Maki and Atsushi Osakada, published by NIKKAN KOGYO SHIMBUN, LTD., 1973) can be used.
The present invention will be more specifically described by way of Examples; however, the present invention is not limited by these Examples.
The materials used in the following Examples and Comparative Examples regarding the heat conductive foam sheet (1) for electronic equipment of the present invention are as follows.
(1) Acrylonitrile butadiene rubber (NBR)
Trade name “Nipol 1041”, manufactured by ZEON CORPORATION
Density: 1.00 g/cm3
Acrylonitrile component: 40.5 mass %
(2) liquid-state acrylonitrile butadiene rubber (liquid-state NBR)
Trade name “Nipol 1312”, manufactured by ZEON CORPORATION,
Density: 0.98 g/cm3
(3) Ethylene-propylene-diene rubber (EPDM)
Trade name “EP21”, manufactured by JSR Corporation,
Density: 0.86 g/cm3
Content of propylene: 34 mass %
(4) Liquid ethylene-propylene-diene rubber (liquid-state EPDM)
Trade name “PX-068”, manufactured by Mitsui Chemicals, Inc.
Density: 0.9 g/cm3
Content of propylene: 39 mass %
(5) Azodicarbonamide
Trade name “SO-L”, manufactured by Otsuka Chemical Co., Ltd.
(6) Aluminum oxide
Trade name “AX3-32”, manufactured by Micron Inc.
Spherical alumina, average particle size: 3 μm
(7) Magnesium oxide
Trade name “RF-10C-SC”, manufactured by Ube Material Industries
Pulverized product, 45 μm or less, sieved average particle size: 4 μm
(8) Phenol oxidant
Trade name “IRGANOX1010”, manufactured by Ciba Specialties Chemicals
100 parts by mass of an acrylonitrile butadiene rubber, 15 parts by mass of azodicarbonamide, 400 parts by mass of aluminum oxide and 0.1 parts by mass of a phenolic antioxidant were melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.4 mm.
To both surfaces of the obtained expandable resin sheet, 1.2 Mrad of an electron beam was applied at an acceleration voltage of 500 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 0.98 g/cm3 and a thickness of 0.5 mm.
80 parts by mass of an acrylonitrile butadiene rubber, 20 parts by mass of a liquid-state acrylonitrile butadiene rubber, 17 parts by mass of azodicarbonamide, 400 parts by mass of aluminum oxide and 0.1 parts by mass of a phenol oxidant were melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.4 mm.
To both surfaces of the obtained expandable resin sheet, 1.4 Mrad of an electron beam was applied at an acceleration voltage of 500 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 1.00 g/cm3 and a thickness of 0.5 mm.
70 parts by mass of an ethylene-propylene-diene rubber, 30 parts by mass of a liquid-state ethylene-propylene-diene rubber, 17 parts by mass of azodicarbonamide, 400 parts by mass of aluminum oxide and 0.1 parts by mass of a phenol oxidant were melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.4 mm.
To both surfaces of the obtained expandable resin sheet, 3.0 Mrad of an electron beam was applied at an acceleration voltage of 500 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 0.70 g/cm3 and a thickness of 0.5 mm.
100 parts by mass of an ethylene-propylene-diene rubber, 17 parts by mass of azodicarbonamide, 400 parts by mass of aluminum oxide and 0.1 parts by mass of a phenol oxidant were melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.43 mm.
To both surfaces of the obtained expandable resin sheet, 3.0 Mrad of an electron beam was applied at an acceleration voltage of 500 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 0.95 g/cm3 and a thickness of 0.5 mm.
100 parts by mass of an ethylene-propylene-diene rubber, 17 parts by mass of azodicarbonamide, 360 parts by mass of magnesium oxide and 0.1 parts by mass of a phenol oxidant were melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.43 mm.
To both surfaces of the obtained expandable resin sheet, 3.0 Mrad of an electron beam was applied at an acceleration voltage of 500 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 0.98 g/cm3 and a thickness of 0.5 mm.
60 parts by mass of an ethylene-propylene-diene rubber, 40 parts by mass of a liquid-state ethylene-propylene-diene rubber, 17 parts by mass of azodicarbonamide, 360 parts by mass of magnesium oxide and 0.1 parts by mass of a phenol oxidant were melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.4 mm.
To both surfaces of the obtained expandable resin sheet, 3.0 Mrad of an electron beam was applied at an acceleration voltage of 500 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 0.60 g/cm3 and a thickness of 0.5 mm.
100 parts by mass of an acrylonitrile butadiene rubber, 6 parts by mass of azodicarbonamide and 0.1 parts by mass were supplied to an extruder, melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.25 mm.
To both surfaces of the obtained expandable resin sheet, 1.2 Mrad of an electron beam was applied at an acceleration voltage of 500 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 0.12 g/cm3 and a thickness of 0.5 mm.
100 parts by mass of an acrylonitrile butadiene rubber, 15 parts by mass of azodicarbonamide, 400 parts by mass of aluminum oxide and 0.1 parts by mass of a phenol oxidant were supplied to an extrusion kneader, melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 1.6 mm.
To both surfaces of the obtained expandable resin sheet, 1.2 Mrad of an electron beam was applied at an acceleration voltage of 1000 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 0.99 g/cm3 and a thickness of 2.0 mm.
100 parts by mass of an acrylonitrile butadiene rubber, 8 parts by mass of azodicarbonamide, 400 parts by mass of aluminum oxide and 0.1 parts by mass of a phenol oxidant were melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.48 mm.
To both surfaces of the obtained expandable resin sheet, 1.2 Mrad of an electron beam was applied at an acceleration voltage of 500 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 1.93 g/cm3 and a thickness of 0.5 mm.
<Physical Properties>
Physical properties of the obtained foam sheets were measured as follows. The measurement results of individual properties are shown in Table 1.
The expansion ratio was calculated by dividing the specific gravity of a foam sheet by the specific gravity of an expandable resin sheet.
Apparent density was measured in accordance with JIS K 7222.
The 25% and 50% compressive strength of a foam sheet in the thickness direction were measured in accordance with JIS K6767-7.2.3 (JIS2009).
The heat conductivity of an unfoamed resin sheet was measured at 25° C. by “TC-7000” manufactured by ULVAC-RIKO, Inc., in accordance with a laser flash method. Thereafter, heat conductivity was computationally obtained as a calculation value based on the following expression and an apparent density.
1/λe={(1−V1/3)/λS}+V1/3/{λS·(1−V2/3)+λg·V2/3}
λe denotes the heat conductivity of foam sheet,
V denotes the porosity of foam sheet (porosity=1−[1/expansion ratio]),
λS denotes the heat conductivity of unfoamed resin sheet,
λg denotes the heat conductivity of air
As shown in
From the results of Examples and Comparative Examples, it is found that the heat conductive foam sheet (1) for electronic equipment of the present invention is thin and flexible as well as excellent in heat conductivity.
The materials used in the following Examples 7 to 10 and Comparative Examples 4 and 5 are as follows.
(1) Butyl rubber
Isobutylene-isoprene rubber manufactured by Exxon,
Trade name “Butyl 065”
Density: 0.92 g/cm3
Mooney viscosity (100° C.)=47 (ML)
Unsaturation degree=2.0
(2) Ethylene-propylene rubber
Model number “EP21”, manufactured by JSR Corporation,
Mooney viscosity (125° C.)=26 (ML)
(3) Ethylene-propylene-diene rubber (EPDM)
Trade name “EP21”, manufactured by JSR Corporation,
Density: 0.86 g/cm3
Content of propylene: 34 mass %
(4) Liquid-state ethylene-propylene-diene rubber (liquid-state EPDM)
Trade name “PX-068”, manufactured by Mitsui Chemicals, Inc.,
Density: 0.9 g/cm3
Content of propylene: 39 mass %
(5) Azodicarbonamide
Trade name “SO-L”, manufactured by Otsuka Chemical Co., Ltd.,
(6) Talc
Trade name “P-6”, manufactured by Nippon Talc Co., Ltd.,
Average particle size: 4 μm
(7) Boron nitride
Trade name “Denka Boron Nitride SGP”, manufactured by Denki Kagaku Kogyo K.K.
Average particle size: 15 μm
(8) Phenol oxidant
Trade name “IRGANOX1010”, manufactured by Ciba Specialties Chemicals
100 parts by mass of a butyl rubber, 16 parts by mass of azodicarbonamide, 200 parts by mass of talc and 0.1 parts by mass of a phenol oxidant were melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.4 mm.
To both surfaces of the obtained expandable resin sheet, 2.5 Mrad of an electron beam was applied at an acceleration voltage of 500 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 0.74 g/cm3 and a thickness of 0.5 mm.
100 parts by mass of a butyl rubber, 16 parts by mass of azodicarbonamide, 220 parts by mass of boron nitride and 0.1 parts by mass of a phenol oxidant were melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.4 mm.
To both surfaces of the obtained expandable resin sheet, 2.5 Mrad of an electron beam was applied at an acceleration voltage of 500 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 0.76 g/cm3 and a thickness of 0.5 mm.
100 parts by mass of an ethylene-propylene rubber, 17.5 parts by mass of azodicarbonamide, 220 parts by mass of boron nitride and 0.1 parts by mass of a phenol oxidant were melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.4 mm.
To both surfaces of the obtained expandable resin sheet, 2.5 Mrad of an electron beam was applied at an acceleration voltage of 500 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 0.74 g/cm3 and a thickness of 0.5 mm.
70 parts by mass of an ethylene-propylene-diene rubber, 30 parts by mass of a liquid-state ethylene-propylene-diene rubber, 17.5 parts by mass of azodicarbonamide, 220 parts by mass of boron nitride and 0.1 parts by mass of a phenol oxidant were melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.38 mm.
To both surfaces of the obtained expandable resin sheet, 3.0 Mrad of an electron beam was applied at an acceleration voltage of 500 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 0.44 g/cm3 and a thickness of 0.5 mm.
A heat dissipation silicon pad (“TC-CAS-10” manufactured by Shin-Etsu Chemical Co., Ltd., thickness: 0.5 mm, heat conductivity: 1.8 W/m·K) was used as Comparative Example 4.
100 parts by mass of an ethylene-propylene rubber, 220 parts by mass of boron nitride and 0.1 parts by mass of a phenol oxidant were melt-kneaded and then pressed to obtain a resin compound sheet having a thickness of 0.5 mm and an apparent density 1.5 g/cm3.
<Physical Properties>
Physical properties of the obtained foam sheets were measured as follows. The measurement results of individual properties are shown in Table 2.
The expansion ratio was calculated by dividing the specific gravity of a foam sheet by the specific gravity of an expandable sheet.
Apparent density was measured in accordance with JIS K 7222.
The 25% compressive strength of a foam sheet in the thickness direction was measured in accordance with JIS K6767-7.2.3 (JIS2009).
The dielectric constant of a foam sheet was measured by an LCR meter in accordance with an automatic balancing bridge method, in the conditions of 1 MHz and a main electrode diameter of 28 ϕ (tin foil is added).
The heat conductivity was measured at 25° C. by “TC-7000” manufactured by ULVAC-RIKO, Inc., in accordance with a laser flash method.
As shown in
From the results of Examples and Comparative Examples, it is found that the heat conductive foam sheet (1) for electronic equipment of the present invention is low in specific dielectric constant, and thin and flexible; at the same time, it has the same heat conductivity as in the silicone sheet.
The materials used in the following Examples and Comparative Examples regarding the heat conductive foam sheet (2) for electronic equipment of the present invention are as follows.
(1) Acrylonitrile butadiene rubber (NBR)
Trade name “Nipol 1041”, manufactured by ZEON CORPORATION
Density: 1.00 g/cm3
Acrylonitrile component: 40.5 mass %
(2) Ethylene-propylene-diene rubber (EPDM)
Trade name “EP21”, manufactured by JSR Corporation,
Density: 0.86 g/cm3
Content of propylene: 34 mass %
(3) Liquid ethylene-propylene-diene rubber (liquid-state EPDM)
Trade name “PX-068”, manufactured by Mitsui Chemicals, Inc.
Density: 0.9 g/cm3
Content of propylene: 39 mass %
(4) Azodicarbonamide
Trade name “SO-L”, manufactured by Otsuka Chemical Co., Ltd.
(5) Graphite
Trade name “XGnP-H-S”, manufactured by XG Sciences,
Shape: scale-like
Major axis: 5 μm in average
Minor axis: 5 μm in average
Thickness: 15 nm in average
Major axis/thickness=5/0.015=333.3
(6) Boron nitride
Trade name “Denka boron nitride SGP”, manufactured by Denki Kagaku Kogyo K.K.,
Shape: Scale-like
Major axis: 15 μm in average
Minor axis: 15 μm in average
Thickness: 3 μm in average
Major axis/thickness=15/3=5
(7) Magnesium oxide
Trade name “RF-10C-SC”, manufactured by Ube Material Industries,
Shape: Round pulverized product
Average particle size: 4 μm
(8) Aluminum oxide
Spherical alumina, trade name “AX3-32”, manufactured by Micron Inc.
Shape: Spherical
Average particle size: 3 μm
(9) Phenol oxidant
Trade name “IRGANOX1010”, manufactured by Ciba Specialties Chemicals
100 parts by mass of an acrylonitrile butadiene rubber, 15 parts by mass of azodicarbonamide, 220 parts by mass of graphite and 0.1 parts by mass of a phenol oxidant were melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.4 mm.
To both surfaces of the obtained expandable resin sheet, 1.2 Mrad of an electron beam was applied at an acceleration voltage of 500 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 0.79 g/cm3 and a thickness of 0.5 mm.
100 parts by mass of an acrylonitrile butadiene rubber, 16 parts by mass of azodicarbonamide, 220 parts by mass of boron nitride and 0.1 parts by mass of a phenol oxidant were melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.4 mm.
To both surfaces of the obtained expandable resin sheet, 1.2 Mrad of an electron beam was applied at an acceleration voltage of 500 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 0.76 g/cm3 and a thickness of 0.5 mm.
70 parts by mass of an ethylene-propylene-diene rubber, 30 parts by mass of a liquid-state ethylene-propylene-diene rubber, 15 parts by mass of azodicarbonamide, 220 parts by mass of graphite and 0.1 parts by mass of a phenol oxidant were melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.4 mm.
To both surfaces of the obtained expandable resin sheet, 3.0 Mrad of an electron beam was applied at an acceleration voltage of 500 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 0.44 g/cm3 and a thickness of 0.5 mm.
70 parts by mass of an ethylene-propylene-diene rubber, 30 parts by mass of a liquid-state ethylene-propylene-diene rubber, 16 parts by mass of azodicarbonamide, 220 parts by mass of boron nitride and 0.1 parts by mass of a phenol oxidant were melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.4 mm.
To both surfaces of the obtained expandable resin sheet, 3.0 Mrad of an electron beam was applied at an acceleration voltage of 500 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 0.42 g/cm3 and a thickness of 0.5 mm.
100 parts by mass of an acrylonitrile butadiene rubber, 15 parts by mass of azodicarbonamide, 360 parts by mass of magnesium oxide and 0.1 parts by mass of a phenol oxidant were supplied to an extruder, melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.4 mm
To both surfaces of the obtained expandable resin sheet, 1.2 Mrad of an electron beam was applied at an acceleration voltage of 500 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 1.03 g/cm3 and a thickness of 0.5 mm.
100 parts by mass of an acrylonitrile butadiene rubber, 15 parts by mass of azodicarbonamide, 400 parts by mass of aluminum oxide and 0.1 parts by mass of a phenol oxidant were melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.4 mm.
To both surfaces of the obtained expandable resin sheet, 1.2 Mrad of an electron beam was applied at an acceleration voltage of 500 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 0.98 g/cm3 and a thickness of 0.5 mm.
60 parts by mass of an ethylene-propylene-diene rubber, 40 parts by mass of a liquid-state ethylene-propylene-diene rubber, 15 parts by mass of azodicarbonamide, 360 parts by mass of magnesium oxide and 0.1 parts by mass of a phenol oxidant were melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.4 mm.
To both surfaces of the obtained expandable resin sheet, 3.0 Mrad of an electron beam was applied at an acceleration voltage of 500 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 0.70 g/cm3 and a thickness of 0.5 mm.
100 parts by mass of an acrylonitrile butadiene rubber, 8 parts by mass of azodicarbonamide, 400 parts by mass of aluminum oxide and 0.1 parts by mass of a phenol oxidant were melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.48 mm.
To both surfaces of the obtained expandable resin sheet, 1.2 Mrad of an electron beam was applied at an acceleration voltage of 500 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 1.93 g/cm3 and a thickness of 0.5 mm.
100 parts by mass of an acrylonitrile butadiene rubber, 6 parts by mass of azodicarbonamide and 0.1 parts by mass of a phenol oxidant were supplied to an extruder, melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.25 mm.
To both surfaces of the obtained expandable resin sheet, 1.2 Mrad of an electron beam was applied at an acceleration voltage of 500 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 0.12 g/cm3 and a thickness of 0.5 mm.
<Physical Properties>
Physical properties of the obtained foam sheets were measured as follows. The measurement results of individual properties are shown in Table 3.
[25% Compressive Strength]
The 25% compressive strengths, i.e., strength during application of 25% compressive strain, of the obtained sheets in the thickness direction were measured in accordance with JIS K6767-7.2.3 (JIS2009).
The expansion ratio was calculated by dividing the specific gravity of a foam sheet by the specific gravity of an expandable sheet.
The heat conductivity was measured at 25° C. by “TC-7000” manufactured by ULVAC-RIKO, Inc., in accordance with a laser flash method.
Apparent density was measured in accordance with JIS K 7222.
As shown in
From the results of Examples and Comparative Examples, it is found that the heat conductive foam sheet (2) for electronic equipment of the present invention is thin and flexible as well as excellent in heat conductivity.
The materials used in the following Examples and Comparative Examples regarding heat conductive laminate for electronic equipment of the present invention are as follows.
(1) Linear low-density polyethylene
Trade name “KERNEL KF370”, manufactured by Japan Polyethylene Corporation,
Density: 1.00 g/cm3
(2) Acrylonitrile butadiene rubber (NBR)
Trade name “Nipol 1041”, manufactured by ZEON CORPORATION
Density: 1.00 g/cm3
Acrylonitrile component: 40.5 mass %
(3) Ethylene-propylene-diene rubber (EPDM)
Trade name “EP21”, manufactured by JSR Corporation,
Density: 0.86 g/cm3
Content of propylene: 34 mass %
(4) Liquid ethylene-propylene-diene rubber (liquid-state EPDM)
Trade name “PX-068”, manufactured by Mitsui Chemicals, Inc.
Density: 0.9 g/cm3
Content of propylene: 39 mass %
(5) Azodicarbonamide
Trade name “SO-L”, manufactured by Otsuka Chemical Co., Ltd.
(6) Aluminum oxide
Trade name “AX3-32”, spherical alumina, manufactured by Micron Inc.,
Average particle size: 3 μm
(7) Magnesium oxide
Trade name “RF-10C-SC”, manufactured by Ube Material Industries,
Round pulverized product
Average particle size: 4 μm
(8) Phenol oxidant
Trade name “IRGANOX1010”, manufactured by Ciba Specialties Chemicals
100 parts by mass of a linear low-density polyethylene obtained by using a metallocene compound as a polymerization catalyst, 3.0 parts by mass of azodicarbonamide and 0.1 parts by mass of a phenol oxidant were melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.36 mm.
To both surfaces of the obtained expandable resin sheet, 4 Mrad of an electron beam was applied at an acceleration voltage of 500 kV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 0.20 g/cm3 and a thickness of 0.5 mm.
To one of the surfaces of the foam sheet obtained, a copper-foil tape (No: 2194 manufactured by 3M) of 150 μm in thickness was bonded to obtain a laminate of the foam sheet and the copper foil.
100 parts by mass of an acrylonitrile butadiene rubber, 15 parts by mass of azodicarbonamide, 400 parts by mass of aluminum oxide and 0.1 parts by mass of a phenol oxidant were melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.4 mm.
To both surfaces of the obtained expandable resin sheet, 1.2 Mrad of an electron beam was applied at an acceleration voltage of 500 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 0.98 g/cm3 and a thickness of 0.5 mm.
To one of the surfaces of the foam sheet obtained, a copper-foil tape (No: 2194 manufactured by 3M) of 150 μm in thickness was bonded to obtain a laminate of the foam sheet and the copper foil.
70 parts by mass of an ethylene-propylene-diene rubber, 30 parts by mass of a liquid-state ethylene-propylene-diene rubber, 17.5 parts by mass of azodicarbonamide, 400 parts by mass of aluminum oxide and 0.1 parts by mass of a phenol oxidant were melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.4 mm.
To both surfaces of the obtained expandable resin sheet, 3.0 Mrad of an electron beam was applied at an acceleration voltage of 500 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 0.47 g/cm3 and a thickness of 0.5 mm.
To one of the surfaces of the foam sheet obtained, a copper-foil tape (No: 2194 manufactured by 3M) of 150 μm in thickness was bonded to obtain a laminate of the foam sheet and the copper foil.
60 parts by mass of an ethylene-propylene-diene rubber, 40 parts by mass of a liquid-state ethylene-propylene-diene rubber, 17 parts by mass of azodicarbonamide, 360 parts by mass of magnesium oxide and 0.1 parts by mass of a phenol oxidant were melt-kneaded and then pressed to obtain an expandable resin sheet having a thickness of 0.4 mm.
To both surfaces of the obtained expandable resin sheet, 3.0 Mrad of an electron beam was applied at an acceleration voltage of 500 keV to crosslink the expandable resin sheet. Subsequently, the sheet was heated to 250° C. to expand the expandable resin sheet to obtain a foam sheet having an apparent density of 0.60 g/cm3 and a thickness of 0.5 mm.
To one of the surfaces of the foam sheet obtained, a copper-foil tape (No: 2194 manufactured by 3M) of 150 μm in thickness was bonded to obtain a laminate of the foam sheet and the copper foil.
A foam sheet was obtained in the same manner as in Example 15 except that a copper foil was not bonded.
A foam sheet was obtained in the same manner as in Example 16 except that a copper foil was not bonded.
A foam sheet was obtained in the same manner as in Example 17 except that a copper foil was not bonded and the expansion ratio was changed as described in Table 4.
A foam sheet was obtained in the same manner as in Example 18 except that that a copper foil was not bonded.
<Physical Properties>
Physical properties of the obtained foam sheets were measured as follows. The measurement results of individual properties are shown in Table 4.
The 25% compressive strength of a foam sheet in the thickness direction was measured in accordance with JIS K6767-7.2.3 (JIS2009)
The expansion ratio was calculated by dividing the specific gravity of a foam sheet by the specific gravity of an expandable sheet.
The heat conductivity was measured at 25° C. by “TC-7000” manufactured by ULVAC-RIKO, Inc. in accordance with a laser flash method.
Apparent density was measured in accordance with JIS K 7222.
[Heat Conductivity]
As shown in
From the results of Examples and Comparative Examples, it is found that the heat conductive laminate for electronic equipment of the present invention is thin and flexible as well as excellent in heat conductivity.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2012-258401 | Nov 2012 | JP | national |
| 2013-070418 | Mar 2013 | JP | national |
| 2013-070420 | Mar 2013 | JP | national |
| 2013-070429 | Mar 2013 | JP | national |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 14647218 | May 2015 | US |
| Child | 16238628 | US |
