JPH0227801B2 - - Google Patents
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- Publication number
- JPH0227801B2 JPH0227801B2 JP58168864A JP16886483A JPH0227801B2 JP H0227801 B2 JPH0227801 B2 JP H0227801B2 JP 58168864 A JP58168864 A JP 58168864A JP 16886483 A JP16886483 A JP 16886483A JP H0227801 B2 JPH0227801 B2 JP H0227801B2
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- JP
- Japan
- Prior art keywords
- ptc element
- heat dissipation
- adhesive layer
- weight
- dissipation structure
- Prior art date
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- Thermistors And Varistors (AREA)
Description
【発明の詳細な説明】
[発明の背景と目的]
本発明はPTC素子の放熱構造に関するもので
ある。DETAILED DESCRIPTION OF THE INVENTION [Background and Objectives of the Invention] The present invention relates to a heat dissipation structure for a PTC element.
PTC素子は正の温度係数を有する抵抗体で、
自己制御性を有する発熱体である。通常チタン酸
バリウムを主体とするセラミツク系のものと、プ
ラスチツクに導電性付与剤を添加したプラスチツ
ク系のものがある。特にセラミツク系のものは信
頼性に優れていることから広範に使用されてい
る。PTC素子は発熱体であるため放熱体と組み
合わせて使用されることが多い。この場合、
PTC素子と放熱体とを一体化させるための接着
剤として、熱伝導性に優れたエポキシ樹脂が使用
されてきた。しかし、PTC素子および金属が主
体である放熱体とエポキシ樹脂の熱膨張係数が異
なるため、冷熱サイクルや熱衝撃の条件において
エポキシ樹脂が破損してしまう欠点があつた。 A PTC element is a resistor with a positive temperature coefficient.
It is a heating element with self-regulating properties. Usually, there are ceramic-based materials mainly made of barium titanate, and plastic-based materials with conductivity imparting agents added to plastic. In particular, ceramic materials are widely used because of their excellent reliability. Since the PTC element is a heat generating element, it is often used in combination with a heat sink. in this case,
Epoxy resin, which has excellent thermal conductivity, has been used as an adhesive to integrate the PTC element and the heat sink. However, because the thermal expansion coefficients of the PTC element and the heat sink, which is mainly made of metal, and the epoxy resin are different, there was a drawback that the epoxy resin could be damaged under conditions of cold/heat cycles or thermal shock.
本発明は上記した従来技術の欠点を解消するも
のであり、急激な温度変化を伴なう条件において
もPTC素子と放熱体とを一体化する接着層の破
損を防止できるPTC素子放熱構造の提供を目的
とするものである。 The present invention solves the above-mentioned drawbacks of the conventional technology, and provides a PTC element heat dissipation structure that can prevent damage to the adhesive layer that integrates the PTC element and the heat dissipation body even under conditions involving rapid temperature changes. The purpose is to
[発明の概要]
本発明は、PTC素子と放熱体との間を、付加
重合型シリコーンゴムと無機充填剤とを含有する
熱伝導性組成物からなる接着層を介して一体化し
たことを特徴とするものである。[Summary of the invention] The present invention is characterized in that a PTC element and a heat sink are integrated through an adhesive layer made of a thermally conductive composition containing an addition polymerizable silicone rubber and an inorganic filler. That is.
PTC素子としては、例えばチタン酸バリウム
に酸化サマリウムのような添加物を微量に加えて
焼結したものに電極を埋め込んだものがあげられ
る。このような正の温度係数を有する素子であれ
ば特に組成を限定するものではない。本発明はセ
ラミツクPTC素子に対して特に有効であるが、
放熱を必要とするプラスチツク系PTC素子に対
しても適用できる。ただ、プラスチツクPTC素
子の場合には、ポリオレフインと導電性付与剤を
主体としたもののように接着が困難なものもある
ので、シランカツプリング剤等でプライマ処理を
行なつてから接着させることが好ましい。 An example of a PTC element is one in which electrodes are embedded in barium titanate with a small amount of an additive such as samarium oxide added and sintered. The composition is not particularly limited as long as the element has such a positive temperature coefficient. Although the present invention is particularly effective for ceramic PTC elements,
It can also be applied to plastic PTC elements that require heat dissipation. However, in the case of plastic PTC elements, some of them are difficult to adhere to, such as those made mainly of polyolefin and conductivity imparting agents, so it is preferable to perform a primer treatment with a silane coupling agent, etc. before adhering. .
放熱体は、通常は銅、銅合金、アルミニウム、
鉄等の金属が実用されるが、腐食をきらう用途で
は黒鉛、炭化ケイ素等の高熱伝導性セラミツクが
使用される。 Heat sinks are usually copper, copper alloys, aluminum,
Metals such as iron are used in practice, but highly thermally conductive ceramics such as graphite and silicon carbide are used in applications where corrosion is to be avoided.
本発明において重要なのは、上記PTC素子と
放熱体を一体化させるための接着層を付加重合型
シリコーンゴムと無機充填剤とを含有する熱伝導
性組成物でもつて形成した点にある。 What is important in the present invention is that the adhesive layer for integrating the PTC element and the heat sink is formed of a thermally conductive composition containing an addition polymerizable silicone rubber and an inorganic filler.
この組成物は金属およびセラミツクの双方に対
して接着力が強く、しかも硬化後も弾性を有する
ため急激な温度変化に伴なう膨張、収縮に追従で
きるものである。 This composition has strong adhesion to both metals and ceramics, and has elasticity even after curing, so it can follow expansion and contraction caused by rapid temperature changes.
また、無機充填剤は付加重合型シリコーンゴム
の熱伝導性を更に向上させるために添加するもの
であるが、無機充填剤はシリコーンゴムに比して
熱膨張係数が小さいため、非充填の場合よりも接
着層の熱膨張係数を金属およびセラミツクのそれ
に近付けることが可能になり、熱衝撃に対する追
従性を更に大きくしている。 In addition, inorganic fillers are added to further improve the thermal conductivity of addition-polymerized silicone rubber, but since inorganic fillers have a smaller coefficient of thermal expansion than silicone rubber, they It is now possible to bring the coefficient of thermal expansion of the adhesive layer closer to that of metal and ceramic, further increasing its ability to respond to thermal shock.
本発明における付加重合型シリコーンゴムとし
ては、
(イ) 1分子中に少なくとも2個のケイ素原子結合
アルケニル基を有するジオルガノポリシロキサ
ン、
(ロ) 1分子中に少なくとも2個のケイ素原子結合
水素原子を有する液状オルガノポリシロキサ
ン、
(ハ) 付加反応触媒、
よりなるものよりなるものがあげられ、成分(ハ)の
触媒作用のもとに架橋されてゴム弾性体を形成す
るものである。かかる付加重合型シリコーンゴム
は、架橋前は液状で、架橋後は優れた粘弾性を有
するものであり、熱伝導性を高める無機充填剤を
充填しても優れた弾力性を長期間にわたり維持で
きることになる。 The addition polymerizable silicone rubber in the present invention includes (a) diorganopolysiloxane having at least two silicon-bonded alkenyl groups in one molecule; (b) at least two silicon-bonded hydrogen atoms in one molecule; and (c) an addition reaction catalyst, which are crosslinked under the catalytic action of component (c) to form a rubber elastic body. Such addition-polymerized silicone rubber is liquid before crosslinking and has excellent viscoelasticity after crosslinking, and can maintain its excellent elasticity for a long period of time even when filled with an inorganic filler that increases thermal conductivity. become.
無機充填剤としては、アルミナ、石英、酸化亜
鉛、マグネシア、窒化ホウ素、窒化アルミニウ
ム、炭化ケイ素、黒鉛、金属等の粉末があげら
れ、これらは単独または2種以上併用して30〜70
容量%の範囲で添加するこつができる。 Examples of inorganic fillers include powders of alumina, quartz, zinc oxide, magnesia, boron nitride, aluminum nitride, silicon carbide, graphite, metals, etc., and these can be used alone or in combination of two or more to give 30 to 70%
You can get the hang of adding it within a volume % range.
本発明においては、上記成分以外に必要に応じ
て粘度を調節するための反応性希釈剤、シリコー
ン油、有機溶剤、ポツトライフを延長するための
ベンゾトリアゾールやハイドロパーオキサイドと
いつた硬化抑制剤、煙霧質シリカのような補強性
充填剤、着色剤、難燃剤等を適宜添加してもよ
い。また、シランカツプリング剤、チタネートカ
ツプリング剤、エポキシ樹脂等を添加することに
より自己接着性を向上できる。 In the present invention, in addition to the above-mentioned components, reactive diluents, silicone oil, organic solvents, curing inhibitors such as benzotriazole and hydroperoxide to extend the pot life, and fumes are used to adjust the viscosity. Reinforcing fillers such as silica, colorants, flame retardants, etc. may be added as appropriate. Furthermore, the self-adhesiveness can be improved by adding a silane coupling agent, a titanate coupling agent, an epoxy resin, or the like.
上記成分よりなる熱伝導性組成物はPTC素子
と放熱体との間に挿入され、その後常温または加
熱により硬化され、両者を一体化する。 A thermally conductive composition made of the above components is inserted between the PTC element and the heat sink, and then cured at room temperature or by heating to integrate the two.
[発明の実施例]
実施例 1
第1図に示すような放熱構造を作用した。1は
チタン酸バリウムを主体とするPTC素子、2は
アルミニウムからなる放熱体、3は熱伝導性組成
物からなる接着層である。[Embodiments of the Invention] Example 1 A heat dissipation structure as shown in FIG. 1 was used. 1 is a PTC element mainly made of barium titanate, 2 is a heat sink made of aluminum, and 3 is an adhesive layer made of a thermally conductive composition.
接着層3を下記(1)〜(7)の成分よりなる組成物で
もつて形成した。 The adhesive layer 3 was formed using a composition consisting of the following components (1) to (7).
(1) 両端をジメチルビニルシリル基で封鎖された
ジメチルポリシロキサン 100重量部
(2) 両末端シラノール基封鎖のジメチルポリシロ
キサン(粘粘度調整剤) 20重量部
(3) 両末端がトリメチルシリル基封鎖メチル水素
ポリシロキサン 12重量部
(4) ビニルトリメトキシシラン 2重量部
(5) アルミナ 350重量部
(6) 塩化白金酸のイソプロピルアルコール1重量
%溶液 1重量部
(7) ベンゾトリアゾールのイソプロピルアルコー
ル30重量%溶液 0.2重量部
上記組成物をPTC素子1と放熱体2の間に挿
入し、150℃で15分間加熱することによつて硬化
させた。(1) 100 parts by weight of dimethylpolysiloxane with both ends blocked with dimethylvinylsilyl groups (2) 20 parts by weight of dimethylpolysiloxane (viscosity modifier) with both ends blocked with silanol groups (3) methyl with both ends blocked with trimethylsilyl groups Hydrogen polysiloxane 12 parts by weight(4) Vinyltrimethoxysilane 2 parts by weight(5) Alumina 350 parts by weight(6) 1% by weight solution of chloroplatinic acid in isopropyl alcohol 1 part by weight(7) 30% by weight of benzotriazole in isopropyl alcohol Solution 0.2 parts by weight The above composition was inserted between the PTC element 1 and the heat sink 2, and cured by heating at 150° C. for 15 minutes.
得られた放熱構造を150℃で30分と−55℃で30
分のサイクル試験を100回繰り返した結果、全く
異常は認められなかつた。また、PTC素子作動
時の放熱特性も良好であつた。 The resulting heat dissipation structure was heated to 150℃ for 30 minutes and -55℃ for 30 minutes.
As a result of repeating the minute cycle test 100 times, no abnormalities were observed. Furthermore, the heat dissipation characteristics during operation of the PTC element were also good.
実施例 2
第2図に示すような放熱構造を作成した。4は
プラスチツク系PTC発熱体、5は鉄製のパイプ
であり、これらの間に実施例1の組成物からベン
ゾトリアゾール溶液を除いた組成物を挿入し、
150℃で15分間加熱して硬化させることにより接
着層6を形成した。Example 2 A heat dissipation structure as shown in FIG. 2 was created. 4 is a plastic PTC heating element, 5 is an iron pipe, and a composition obtained by removing the benzotriazole solution from the composition of Example 1 is inserted between them,
The adhesive layer 6 was formed by heating and curing at 150° C. for 15 minutes.
なお、プラスチツク系PTC抵抗体4は次のよ
うにして製造した。 The plastic PTC resistor 4 was manufactured as follows.
(イ) ポリエチレン(密度0.94、MI:0.3)
100重量部
(ロ) 導電性フアーネスカーボン(XC−72)
30重量部
(ハ) トリメチロールプロパントリメチルメタクリ
レート 2重量部
(ニ) ポリ−2,2,4−トリメチル−1,2−ジ
ヒドロキノリン 1重量部
を均一に混合した組成物を2本のスズメツキ銅線
上に押し出した後、絶縁体を被覆し、20Mradの
電子線を照射して架橋させた。(a) Polyethylene (density 0.94, MI: 0.3)
100 parts by weight (b) Conductive furnace carbon (XC-72)
30 parts by weight (c) 2 parts by weight of trimethylolpropane trimethyl methacrylate (d) 1 part by weight of poly-2,2,4-trimethyl-1,2-dihydroquinoline. After extrusion, it was covered with an insulator and cross-linked by irradiation with a 20 Mrad electron beam.
得られた放熱構造を実施例1と同様のサイクル
試験を100回繰り返した結果全く異常は認められ
なかつた。また、PTC抵抗体4を作動させた場
合の放熱特性も良好であつた。 The obtained heat dissipation structure was subjected to the same cycle test as in Example 1 100 times, and no abnormalities were observed. Furthermore, the heat dissipation characteristics when the PTC resistor 4 was activated were also good.
比較例 1
実施例1の放熱構造において、接着層3を熱伝
導性ビスフエノール系エポキシ樹脂でもつて形成
した。Comparative Example 1 In the heat dissipation structure of Example 1, the adhesive layer 3 was formed using a thermally conductive bisphenol epoxy resin.
実施例1と同様のサイクル試験を行なつた結
果、20回以内で接着層に亀裂もしくは剥離を生じ
た。 As a result of carrying out the same cycle test as in Example 1, the adhesive layer cracked or peeled within 20 cycles.
比較例 2
実施例1の放熱構造において、アルミナを含ま
ない組成物でもつて接着層3を形成した。Comparative Example 2 In the heat dissipation structure of Example 1, the adhesive layer 3 was formed using a composition that did not contain alumina.
実施例1と同様のサイクル試験を行なつた結
果、100繰り返した場合亀裂の発生はなかつたが、
若干の剥離が認められた。また、PTC素子4を
作動させた場合の放熱特性は悪かつた。 As a result of conducting the same cycle test as in Example 1, no cracks occurred after 100 repetitions, but
Some peeling was observed. Furthermore, the heat dissipation characteristics when the PTC element 4 was activated were poor.
[発明の効果]
以上説明してきた通り、本発明は付加重合型シ
リコーンゴムと無機充填剤とを含有する熱伝導性
組成物でもつてPTC素子と放熱体とを一体化し
たPTC素子の放熱構造を提供するものであり、
これによつて苛酷な熱衝撃に対して十分耐える放
熱構造を得ることができる。しかも本発明のおい
てはPTC素子から放熱体への熱伝導性は極めて
良好であり、PTC素子の寿命を長くすることが
可能となる。また、本発明の接着層は付加重合型
シリコーンゴムにより形成するため、腐食性物質
を生成しないので金属を腐食させることがない。[Effects of the Invention] As explained above, the present invention provides a heat dissipation structure for a PTC element that integrates a PTC element and a heat dissipation body using a thermally conductive composition containing an addition polymerized silicone rubber and an inorganic filler. It is intended to provide
This makes it possible to obtain a heat dissipation structure that can sufficiently withstand severe thermal shock. Moreover, according to the present invention, the thermal conductivity from the PTC element to the heat sink is extremely good, making it possible to extend the life of the PTC element. Furthermore, since the adhesive layer of the present invention is formed from addition polymerized silicone rubber, it does not generate corrosive substances and therefore does not corrode metal.
第1図は実施例1および比較例1、2の説明
図、第2図は実施例2の説明図である。
1:PTC素子、2:放熱体、3:接着層。
FIG. 1 is an explanatory diagram of Example 1 and Comparative Examples 1 and 2, and FIG. 2 is an explanatory diagram of Example 2. 1: PTC element, 2: heat sink, 3: adhesive layer.
Claims (1)
なくとも2個のケイ素原子結合アルケニル基を有
するジオルガノポリシロキサンと、1分子中に少
なくとも2個のケイ素原子結合水素原子を有する
液状オルガノポリシロキサンと、付加反応触媒か
らなる付加重合型シリコーンゴムに無機充填剤を
混合した熱伝導性組成物からなる接着層を介して
一体化したことを特徴とするPTC素子放熱構造。1 A diorganopolysiloxane having at least two silicon-bonded alkenyl groups in one molecule and a liquid organopolymer having at least two silicon-bonded hydrogen atoms in one molecule are used between the PTC element and the heat sink. A PTC element heat dissipation structure characterized by being integrated via an adhesive layer made of a thermally conductive composition made of an addition-polymerized silicone rubber made of siloxane and an addition reaction catalyst mixed with an inorganic filler.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16886483A JPS6059704A (en) | 1983-09-13 | 1983-09-13 | Ptc element heat sink structure |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16886483A JPS6059704A (en) | 1983-09-13 | 1983-09-13 | Ptc element heat sink structure |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6059704A JPS6059704A (en) | 1985-04-06 |
| JPH0227801B2 true JPH0227801B2 (en) | 1990-06-20 |
Family
ID=15875970
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP16886483A Granted JPS6059704A (en) | 1983-09-13 | 1983-09-13 | Ptc element heat sink structure |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6059704A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6221972A (en) * | 1985-07-23 | 1987-01-30 | 日本テキサス・インスツルメンツ株式会社 | Key hole heater |
| JP4999528B2 (en) * | 2007-04-20 | 2012-08-15 | ニチコン株式会社 | Positive characteristic thermistor device and manufacturing method thereof |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS476832U (en) * | 1971-02-17 | 1972-09-25 | ||
| JPS575836B2 (en) * | 1974-03-19 | 1982-02-02 | ||
| JPS528040U (en) * | 1975-07-04 | 1977-01-20 | ||
| JPS5222965A (en) * | 1975-08-14 | 1977-02-21 | Matsushita Electric Ind Co Ltd | Frequency voltage converting device |
| JPS595219B2 (en) * | 1976-09-08 | 1984-02-03 | 東芝シリコ−ン株式会社 | Polyorganosiloxane composition that can be cured into a rubbery state |
| JPS5350818U (en) * | 1976-10-04 | 1978-04-28 | ||
| JPS562349A (en) * | 1979-06-21 | 1981-01-12 | Toshiba Silicone Co Ltd | Molded rubber article for heat dissipation |
| JPS56155501A (en) * | 1980-04-30 | 1981-12-01 | Nippon Denso Co | Resistor |
-
1983
- 1983-09-13 JP JP16886483A patent/JPS6059704A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6059704A (en) | 1985-04-06 |
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