JPS61101524A - Sealing resin composition - Google Patents

Sealing resin composition

Info

Publication number
JPS61101524A
JPS61101524A JP22305884A JP22305884A JPS61101524A JP S61101524 A JPS61101524 A JP S61101524A JP 22305884 A JP22305884 A JP 22305884A JP 22305884 A JP22305884 A JP 22305884A JP S61101524 A JPS61101524 A JP S61101524A
Authority
JP
Japan
Prior art keywords
resin composition
resin
sealing resin
magnesium oxide
epoxy
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP22305884A
Other languages
Japanese (ja)
Inventor
Tsutomu Nagata
勉 永田
Tatsuo Sato
辰雄 佐藤
Takeshi Ono
猛 大野
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kyocera Chemical Corp
Original Assignee
Toshiba Chemical Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Toshiba Chemical Corp filed Critical Toshiba Chemical Corp
Priority to JP22305884A priority Critical patent/JPS61101524A/en
Publication of JPS61101524A publication Critical patent/JPS61101524A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To improve the thermal conductivity, moisture resistance, etc., by adding magnesium oxide powder at a specified weight ratio to an electronic part-sealing resin composition based on an epoxy resin and a novolak phenolic resin as a curing agent. CONSTITUTION:The purpose sealing resin composition is obtained by mixing an epoxy resin (A) with a novolak phenolic resin (B) and 25-90wt% small- diameter magnesium oxide powder (C) of an average particle diameter >=60 mesh at a molar ratio of epoxy groups in component A to phenolic hydroxyl groups in component B of 0.1-10. If desired, a mold release, a flame retardant, a colorant, a cure accelerator, etc., may be added to the composition. Because of its large thermal conductivity, the obtained sealing resin composition shows excellent heat radiation and particularly effective when used in devices such as power semiconductors of a large power consumption.

Description

【発明の詳細な説明】 [発明の技術分野] 本発明は、熱伝尋率が大きく、しかも成形性および金型
の耐摩耗性に優れた特性バランスのよい封止用樹脂組成
物に関する。
DETAILED DESCRIPTION OF THE INVENTION [Technical Field of the Invention] The present invention relates to a resin composition for sealing that has a high thermal conductivity, excellent moldability and mold abrasion resistance, and has well-balanced properties.

[発明の技術的背景とその問題点1 従来、ダイオード、トランジスタ、集積回路等の電子部
品を熱硬化性樹脂を用いて樹脂封止する方法が行われて
きた。 この樹脂封止は、ガラス、金属、セラミックを
用いたハーメチックシール方式に比較して経済的に有利
なため、広く実用化されている。 封止用樹脂としては
、熱硬化性樹脂の中でも信頼性および価格の点からエポ
キシ樹脂が最も一般的に用いられている。 エポキシ1
1脂には、酸無水物、芳香族アミン、ノボラック型フェ
ノール樹脂等の硬化剤が用いられている。 これらの中
でノボラック型フェノール樹脂を硬化剤としたエポキシ
樹脂は、他の硬化剤を使用したものに比べて、成形性、
耐湿性に優れ、毒性がなく、かつ、安価であるため半導
体封止用樹脂として広く使用されている。 また充填剤
としては溶融シリカ粉末や活量性シリカ粉末が前述の硬
化剤と共に最も一般的に使用されている。 近年、半導
体部品の高密度化、大電力化に伴ない熱放散性のより良
い半導体封止用樹脂が要望されてきた。
[Technical Background of the Invention and Problems Thereof 1 Conventionally, a method has been used in which electronic components such as diodes, transistors, and integrated circuits are sealed with a thermosetting resin. This resin sealing is economically advantageous compared to hermetic sealing methods using glass, metal, or ceramic, and is therefore widely put into practical use. Among thermosetting resins, epoxy resin is most commonly used as the sealing resin in terms of reliability and cost. Epoxy 1
For 1 fat, curing agents such as acid anhydrides, aromatic amines, novolac type phenolic resins, etc. are used. Among these, epoxy resins using novolac type phenolic resin as a curing agent have better moldability and better moldability than those using other curing agents.
It is widely used as a semiconductor encapsulation resin because it has excellent moisture resistance, is nontoxic, and is inexpensive. Further, as a filler, fused silica powder or activated silica powder is most commonly used together with the above-mentioned curing agent. BACKGROUND ART In recent years, with the increase in the density and power consumption of semiconductor components, there has been a demand for semiconductor encapsulation resins with better heat dissipation properties.

しかしながら、ノボラック型フェノール樹脂を硬化剤と
したエポキシ樹脂と、溶融シリカ粉末とからなる樹脂組
成物は、熱膨張係数が小さく、耐湿性がよく、潟寒サイ
クル試験によるボンディングワイヤのオープン、樹脂ク
ラック、ペレットクラック等に優れているという特徴を
有するものの、熱伝導率が小さいため熱放散が悪く、消
費電力の大きいパワー半導体では、その機能が果せなく
な−る欠点がある。 一方ノボラック型フェノール樹脂
を硬化剤としたエポキシ樹脂と、結晶性シリカ粉末とか
らなる樹脂組成物は、結晶性シリカ粉末の配合割合を上
げると熱伝導率が大きくなって、熱放散も良好となるが
、耐湿性に対する信頼性が悪くなる欠点がある。 更に
この樹脂組成物から得られる成形品は機械的特性や成形
性が低下する傾向があり、また金型の摩耗が茗しく大き
くなる欠点があった。 従って、シリカ粉末を用いる封
止用樹脂組成物の高熱伝導化にはおのずから限界があっ
た。
However, a resin composition consisting of an epoxy resin using a novolac-type phenolic resin as a curing agent and fused silica powder has a small coefficient of thermal expansion, good moisture resistance, and no open bonding wires or resin cracks in the Lagoon cycle test. Although it has the characteristic of being excellent in preventing pellet cracks, etc., it has a drawback that it has poor heat dissipation due to its low thermal conductivity, and cannot perform its function in power semiconductors with large power consumption. On the other hand, in a resin composition consisting of an epoxy resin using a novolak type phenol resin as a curing agent and crystalline silica powder, increasing the blending ratio of crystalline silica powder increases the thermal conductivity and improves heat dissipation. However, it has the disadvantage of poor reliability in moisture resistance. Furthermore, molded articles obtained from this resin composition tend to have poor mechanical properties and moldability, and also have the disadvantage that mold wear becomes slow and large. Therefore, there is a natural limit to the ability to increase the thermal conductivity of a sealing resin composition using silica powder.

[発明の目的] 本発明は、前記の欠点を解消するためになされたもので
、その目的は、熱伝導率が大きく、熱放散性のよい、成
形性と金型の耐摩耗性に優れ、かつ耐湿性に対する信頼
性の高い、特性バランスのよい封止用樹脂組成物を提供
しようとするものである。
[Object of the Invention] The present invention has been made in order to eliminate the above-mentioned drawbacks, and its purpose is to provide a material with high thermal conductivity, good heat dissipation, excellent moldability and mold abrasion resistance, The present invention also aims to provide a sealing resin composition that is highly reliable in terms of moisture resistance and has well-balanced properties.

[発明の概要] 本発明者らは、上記の目的を達成すべく鋭意研−究を重
ねた結果、酸化マグネシウム粉末を配合することによっ
て、熱伝8I率が大きく、成形性と金型の耐摩耗性に優
れた樹脂組成物がIJられることを見いだし、本り明に
至ったものである。
[Summary of the Invention] As a result of intensive research to achieve the above object, the present inventors found that by blending magnesium oxide powder, the heat transfer rate is high, the moldability and the durability of the mold are improved. The present invention was achieved by discovering that a resin composition with excellent abrasion properties can be used for IJ.

即ち、本発明は、 (A)エポキシ樹脂 (B)ノボラック型フェノール樹脂および(C)酸化マ
グネシウム粉末 を必須成分とし、かつ、前記(Call化マグネシウム
粉末を樹脂組成物に対して25〜90重量%含有させる
ことを特徴とする封止用樹脂組成物である。
That is, the present invention has (A) an epoxy resin, (B) a novolak type phenol resin, and (C) a magnesium oxide powder as essential components, and the above-mentioned (Called magnesium powder) in an amount of 25 to 90% by weight based on the resin composition. This is a sealing resin composition characterized by containing:

本発明に用いる(A>エポキシ樹脂は、その分子中にエ
ポキシ基<8 )を少なくとも2個有する化合物である
かぎり、分子構造、分子量等に特に制限はなく、一般に
使用されているものを広く包含することができる。 例
えばビスフェノール型の芳香族系、シクロヘキサン誘導
体等の脂環族系、さらに次の一般式で示されるエポキシ
ノボラック系等のエポキシ樹脂が挙げられる。″ (式中、R1は水素原子、ハロゲン原子又はアルキル基
を、R2は水素原子又はアルキル基を、nは1以上の整
数を表す)。 これらのエポキシ樹脂は車通又は2種以
上混合して用いる。
The (A) epoxy resin used in the present invention is not particularly limited in molecular structure, molecular weight, etc., as long as it is a compound having at least two epoxy groups <8 in its molecule, and includes a wide range of commonly used resins. can do. Examples include aromatic resins such as bisphenol type, alicyclic resins such as cyclohexane derivatives, and epoxy resins such as epoxy novolak resins represented by the following general formula. (In the formula, R1 represents a hydrogen atom, a halogen atom, or an alkyl group, R2 represents a hydrogen atom or an alkyl group, and n represents an integer of 1 or more.) use

本発明に用いる(B)ノボラック型フェノール樹脂とし
ては、フェノール、アルキルフェノール等のフェノール
類とホルムアルデヒドあるいはパラホルムアルデヒドを
反応させて得られるノボラック型フェノール樹脂および
これらの変性樹脂、例えばエポキシ化もしくはブチル化
ノボラック型フェノール樹脂等が挙げられ、これらは単
独又は2種以上混合して用いる。 ノボラック型フェノ
ール樹脂の配合割合は、前記(A>エポキシ樹脂のエポ
キシW(a)と(B)ノボラック型フェノール樹脂のフ
ェノール性水酸1(b)とのモル比(a/b )が0.
1〜10の範囲であることが必要である。 モル比が0
.1未満もしくは10を超えると耐湿性、成形作業性お
よび硬化物の電気特性が悪くなりいずれの場合も好まし
くない。
The (B) novolak type phenolic resin used in the present invention includes novolak type phenol resins obtained by reacting phenols such as phenol and alkylphenols with formaldehyde or paraformaldehyde, and modified resins thereof, such as epoxidized or butylated novolak types. Examples include phenol resins, and these may be used alone or in combination of two or more. The blending ratio of the novolac type phenolic resin is such that the molar ratio (a/b) of the epoxy W (a) of the (A>epoxy resin) and the phenolic hydroxy acid 1 (b) of the novolac type phenol resin (B) is 0.
It needs to be in the range of 1 to 10. molar ratio is 0
.. If it is less than 1 or more than 10, the moisture resistance, molding workability, and electrical properties of the cured product will deteriorate, which is not preferable.

本発明に用いる(C)酸化マグネシウム粉末としては、
特に制限はなくどのようなものでもよく、例えば焼成酸
化マグネシウム(旭硝子社製#5000)!融マグネシ
ア(赤穂化成社製FMF−’E’ )等が挙げられ、こ
れらは単独又は混合して使用される。 酸化マグネシウ
ム粉末の配合割合は、樹脂組成物に対して25〜90重
量%であることが必要である。 配合量が25重量%未
満では、熱膨張係数が大きく、また熱伝導率が小さくて
好ましくない。 また90重伍%を超えるとかさぼりが
大きく、かつ、成形性が悪くて実用に適さhい。
The (C) magnesium oxide powder used in the present invention is as follows:
There are no particular restrictions and any material may be used, such as calcined magnesium oxide (#5000 manufactured by Asahi Glass Co., Ltd.)! Examples include fused magnesia (FMF-'E' manufactured by Ako Kasei Co., Ltd.), which may be used alone or in combination. The blending ratio of magnesium oxide powder needs to be 25 to 90% by weight based on the resin composition. If the amount is less than 25% by weight, the coefficient of thermal expansion will be large and the thermal conductivity will be low, which is not preferable. Moreover, if it exceeds 90% by weight, bulk will be large and moldability will be poor, making it unsuitable for practical use.

従って上記の範囲に限定される。 酸化マグネシウム粉
末の平均粒子径は60メツシュ以上の細径であることが
必要である。 60メツシュ未満の粒子径の場合は、成
形時にワイヤゲート詰りゃワイヤ流れ、金型摩耗等が生
じて好ましくない。
Therefore, it is limited to the above range. The average particle diameter of the magnesium oxide powder must be 60 mesh or more. If the particle size is less than 60 mesh, it is not preferable because wire gate clogging occurs during molding, wire flow, mold wear, etc.

本発明の封止用樹脂組成物は、エポキシ樹脂、ノボラッ
ク型フェノール樹脂、酸化°マグネシウム粉末を必須成
分とするが、必要に応じて、例えば天然ワックス類、合
成ワックス類、直鎖脂肪酸の金属塩、酸アミド類、エス
テル類、パラフィン類等の離型剤、塩素化パラフィン、
ブロムトルエン、ヘキサブロムベンゼン、三酸化アンチ
モン等の難燃剤、カーボンブラック、ベンガラ等の着色
剤、シランカップリング剤、種々の硬化促進剤などを適
宜添加配合してもよい。
The sealing resin composition of the present invention contains an epoxy resin, a novolac type phenol resin, and a magnesium oxide powder as essential components, but may optionally contain natural waxes, synthetic waxes, metal salts of straight chain fatty acids, etc. , release agents such as acid amides, esters, paraffins, chlorinated paraffins,
Flame retardants such as bromotoluene, hexabromobenzene, and antimony trioxide, colorants such as carbon black and red iron oxide, silane coupling agents, various curing accelerators, and the like may be appropriately added and blended.

本発明の封止用樹脂組成物を成形材料として調製すする
場合の一般的な方法としては、エポキシ樹脂、ノボラッ
ク型フェノール樹脂、酸化マグネシウム粉末、その他を
所定の組成比に選択・した原料組成分をミキサー等によ
って十分均一に混合した後、更に熱ロールによる溶融混
合処理、又はニーダ等による混合処理を行い、次いで冷
却固化させ、適当な大きさに粉砕して成形材料とするこ
とができる。 こうして得た成形材料は、電子部品或い
は電気部品の封止、被覆、絶縁等に適用すれば優れた特
性と信頼性を付与することができる。
A general method for preparing the sealing resin composition of the present invention as a molding material is to use a raw material composition in which epoxy resin, novolak type phenol resin, magnesium oxide powder, and others are selected in a predetermined composition ratio. After sufficiently uniformly mixing with a mixer or the like, the mixture can be further melt-mixed using hot rolls or mixed using a kneader, etc., then cooled and solidified, and pulverized to an appropriate size to form a molding material. The molding material thus obtained can provide excellent properties and reliability when applied to sealing, covering, insulating, etc. electronic or electrical components.

[発明の効果] 本発明の封止用樹脂組成物は、熱伝導率が大きく、熱放
散性がよく成形性と金型の耐摩耗性に優れており、また
耐湿性がよく、温室サイクル試験のボンディングワイヤ
のオープン、樹脂クラック、ベレットクラック等がなく
、消費電力の大きいパワー半導体等の機器に使用して効
果がある。 本発明の樹脂組成物は、特性バランスがよ
く電子・電気部品の封止用として優れた信頼性を付与す
ることができる。
[Effects of the Invention] The sealing resin composition of the present invention has high thermal conductivity, good heat dissipation, excellent moldability and mold abrasion resistance, and has good moisture resistance and has passed greenhouse cycle tests. There are no open bonding wires, resin cracks, pellet cracks, etc., making it effective for use in devices such as power semiconductors that consume large amounts of power. The resin composition of the present invention has well-balanced properties and can provide excellent reliability when used for sealing electronic and electrical components.

[発明の実施例] 本発明を実施例により°具体的に説明するが、本発明は
以下の実施例に限定されるものではない。
[Examples of the Invention] The present invention will be specifically explained with reference to Examples, but the present invention is not limited to the following Examples.

実施例および比較例において1%」とあるのは「重量%
」を意味する。
In Examples and Comparative Examples, "1%" means "wt%"
” means.

実施例 1 クレゾールノボラックエポキシ樹脂(エポキシ当Q 2
15) 18%に、ノボラック型フェノール樹脂(フェ
ノール化W 107)  9%、酸化マグネシウムわ)
末(平均粒径15μm)70%、離型剤等3%を常温で
混合し、更に90〜95℃で混練して封止用樹脂組成物
を製造した。 これを冷却した後粉砕して成形材料とし
、成形材料をタブレット化し、予熱してトランスファー
成形で110℃に加熱した金型内に注入し硬化させて成
形品を得た。 得られた成形品について、熱伝導率、成
形性等の緒特性を試験した。 その結果を第1表に示し
た。
Example 1 Cresol novolac epoxy resin (epoxy weight Q 2
15) 18%, novolak type phenolic resin (phenolized W 107) 9%, magnesium oxide)
70% powder (average particle size 15 μm), 3% mold release agent, etc. were mixed at room temperature, and further kneaded at 90 to 95° C. to produce a sealing resin composition. After cooling, this was crushed to obtain a molding material. The molding material was made into a tablet, and the molded product was injected into a mold that had been preheated and heated to 110° C. by transfer molding and hardened. The obtained molded product was tested for thermal conductivity, moldability, and other properties. The results are shown in Table 1.

実施例 2 実施例1における酸化マグネシウム粉末単体の代わりに
、酸化マグネシウム粉末(平均粒径15μ1)30%と
結晶性シリカ粉末(平均粒径28μm)40%を用いた
以外はすべて実施例1と同一にして樹脂組成物、成形材
料、成形品を得、成形品の緒特性を試験した。 その結
果を第1表に示した。
Example 2 Everything was the same as Example 1 except that 30% of magnesium oxide powder (average particle size 15 μm) and 40% crystalline silica powder (average particle size 28 μm) were used instead of the magnesium oxide powder alone in Example 1. A resin composition, a molding material, and a molded article were obtained, and the properties of the molded article were tested. The results are shown in Table 1.

比較例 1 タレゾールノボラックエポキシ樹脂(エポキシ当ffi
 215) 18%に、ノボラック型フェノール樹脂(
フェノール化fi 107)  9%、溶融シリカ粉末
70%、離型剤等3%を実施例1と同様に操作処理して
樹脂組成物、成形材料、成形品を得た。 得られた成形
品について緒特性を試験したのでその結果を第1表に示
した。
Comparative example 1 Talesol novolac epoxy resin (epoxy
215) 18%, novolak type phenolic resin (
Phenolized fi 107) 9%, fused silica powder 70%, mold release agent, etc. 3% were treated in the same manner as in Example 1 to obtain a resin composition, a molding material, and a molded article. The obtained molded product was tested for mechanical properties and the results are shown in Table 1.

比較例 2 比較例1における溶融シリカ粉末の代わりに結晶性シリ
カ粉末(平均粒径28μm)を用いた以外はづべて比較
例1と同一にして樹脂組成物、成形材料、成形品を得た
。 成形品について2特性を試験したのでその結果を第
1表に示した。
Comparative Example 2 A resin composition, molding material, and molded article were obtained in the same manner as in Comparative Example 1 except that crystalline silica powder (average particle size 28 μm) was used instead of the fused silica powder in Comparative Example 1. . The molded product was tested for two properties, and the results are shown in Table 1.

比較例 3 クレゾールノボラックエポキシ樹脂(エポキシ当In 
2+5) 10%に、ノボラック型フェノール樹脂(フ
ェノール当51107)  5%、結晶性シリカ粉末(
平均粒径28μm)85%を用いた以外はすべて比較例
1と同一にして樹脂組成物、成形材料、成形品を得た。
Comparative Example 3 Cresol novolak epoxy resin (epoxy
2+5) 10%, novolak type phenolic resin (phenol 51107) 5%, crystalline silica powder (
A resin composition, a molding material, and a molded article were obtained in the same manner as in Comparative Example 1 except that 85% (average particle size: 28 μm) was used.

 成形品について2特性を試験したのでその結果を第1
表に示した。
Since we tested two characteristics of the molded product, we will use the results in the first
Shown in the table.

第1表 *1 、得られた成形品を迅速熱伝導計(昭和電工社製
商品名QT〜1−MD)を用いて!1下で測定した
Table 1 *1 The obtained molded product was measured using a rapid thermal conductivity meter (product name: QT~1-MD, manufactured by Showa Denko)! Measured under 1

Claims (1)

【特許請求の範囲】 1(A)エポキシ樹脂 (B)ノボラック型フェノール樹脂および (C)酸化マグネシウム粉末 を必須成分としかつ、前記(C)酸化マグネシウム粉末
を樹脂組成物に対して25〜90重量%含有させること
を特徴とする封止用樹脂組成物。 2 エポキシ樹脂のエポキシ基(a)と、ノボラック型
フェノール樹脂のフェノール性水酸基(b)のモル比(
a/b)が、0.1〜10の範囲であることを特徴とす
る特許請求の範囲第1項記載の封止用樹脂組成物。 3 酸化マグネシウム粉末の平均粒子径が、60メッシ
ュ以上の細径であることを特徴とする特許請求の範囲第
1項又は第2項記載の封止用樹脂組成物。
[Scope of Claims] 1 (A) an epoxy resin, (B) a novolak type phenol resin, and (C) a magnesium oxide powder are essential components, and the (C) magnesium oxide powder is contained in an amount of 25 to 90% by weight based on the resin composition. % of the sealing resin composition. 2 The molar ratio of the epoxy group (a) of the epoxy resin to the phenolic hydroxyl group (b) of the novolac type phenolic resin (
The sealing resin composition according to claim 1, wherein a/b) is in the range of 0.1 to 10. 3. The sealing resin composition according to claim 1 or 2, wherein the magnesium oxide powder has an average particle size of 60 mesh or more.
JP22305884A 1984-10-25 1984-10-25 Sealing resin composition Pending JPS61101524A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP22305884A JPS61101524A (en) 1984-10-25 1984-10-25 Sealing resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22305884A JPS61101524A (en) 1984-10-25 1984-10-25 Sealing resin composition

Publications (1)

Publication Number Publication Date
JPS61101524A true JPS61101524A (en) 1986-05-20

Family

ID=16792170

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22305884A Pending JPS61101524A (en) 1984-10-25 1984-10-25 Sealing resin composition

Country Status (1)

Country Link
JP (1) JPS61101524A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6218441A (en) * 1985-07-17 1987-01-27 Ube Ind Ltd Resin composition for sealing electronic component
JP2012149194A (en) * 2011-01-20 2012-08-09 Panasonic Corp Epoxy resin composition for sealing semiconductor, and semiconductor device
CN106832222A (en) * 2015-12-03 2017-06-13 财团法人工业技术研究院 Epoxy resin composition and thermal interface material comprising same

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5053432A (en) * 1973-09-12 1975-05-12
JPS58119655A (en) * 1982-01-08 1983-07-16 Toshiba Corp Resin sealed type semiconductor device
JPS58198525A (en) * 1982-05-14 1983-11-18 Sanyurejin Kk Epoxy resin composition

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5053432A (en) * 1973-09-12 1975-05-12
JPS58119655A (en) * 1982-01-08 1983-07-16 Toshiba Corp Resin sealed type semiconductor device
JPS58198525A (en) * 1982-05-14 1983-11-18 Sanyurejin Kk Epoxy resin composition

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6218441A (en) * 1985-07-17 1987-01-27 Ube Ind Ltd Resin composition for sealing electronic component
JP2012149194A (en) * 2011-01-20 2012-08-09 Panasonic Corp Epoxy resin composition for sealing semiconductor, and semiconductor device
CN106832222A (en) * 2015-12-03 2017-06-13 财团法人工业技术研究院 Epoxy resin composition and thermal interface material comprising same
CN106832222B (en) * 2015-12-03 2019-06-18 财团法人工业技术研究院 Epoxy resin composition and thermal interface material comprising same

Similar Documents

Publication Publication Date Title
JPH05239321A (en) Epoxy resin composition and semiconductor-sealing arrangement
JPH059270A (en) Resin composition and its manufacture
JPH0468345B2 (en)
JPS61101522A (en) Sealing resin composition
JPH05247181A (en) Epoxy resin composition and semiconductor sealing device
JPS61101524A (en) Sealing resin composition
JPS61101523A (en) Sealing resin composition
JPH0717730B2 (en) Sealing resin composition
JPH0249329B2 (en)
JP2862928B2 (en) Sealing resin composition and semiconductor sealing device
JP2004115747A (en) Resin composition for forming heat sink and device for encapsulating electronic part
JPH0621152B2 (en) Sealing resin composition
JP2857441B2 (en) Sealing resin composition and semiconductor sealing device
JPS60161423A (en) Resin composition for sealing
JPH0739471B2 (en) Sealing resin composition
JPH0258525A (en) Resin composition for sealing use
JPS6143621A (en) Sealing resin composition
JPH03142956A (en) Resin sealed type semiconductor device
JPH0343445A (en) Sealing resin composition and its sealed semiconductor device
JPS60152522A (en) Sealing resin composition
JPH0562612B2 (en)
JP3506423B2 (en) Sealing resin composition and semiconductor sealing device
JPH0753671A (en) Epoxy resin composition and sealed semiconductor device
JP3298084B2 (en) Sealing resin composition and semiconductor sealing device
JPH0747681B2 (en) Sealing resin composition