JPS61166823A - Resin composition for sealing - Google Patents

Resin composition for sealing

Info

Publication number
JPS61166823A
JPS61166823A JP669385A JP669385A JPS61166823A JP S61166823 A JPS61166823 A JP S61166823A JP 669385 A JP669385 A JP 669385A JP 669385 A JP669385 A JP 669385A JP S61166823 A JPS61166823 A JP S61166823A
Authority
JP
Japan
Prior art keywords
group
resin
epoxy
resin composition
sealing
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
JP669385A
Other languages
Japanese (ja)
Inventor
Tsutomu Nagata
勉 永田
Tatsuo Sato
辰雄 佐藤
Hiroyuki Hosokawa
洋行 細川
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 JP669385A priority Critical patent/JPS61166823A/en
Publication of JPS61166823A publication Critical patent/JPS61166823A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Epoxy Resins (AREA)
  • Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)

Abstract

PURPOSE:To provide the titled composition having high adhesivity and excellent moisture resistance and giving small stress to semiconductor element pellet, by adding an alkaline earth metal oxide and an organopolysiloxane having a specific group to an epoxy resin composition. CONSTITUTION:The objective composition is composed essentially of (A) an epoxy resin (a compound having >=2 epoxy groups in a molecule), (B) a novolac- type phenolic resin, (C) an alkaline earth metal oxide (preferably CaO, CaO2, BaO or BaO2 having a particle diameter of 0.01-3mu), (D) an organopolysiloxane having epoxy group, amino group, carboxyl group, OH group and/or cyano group in the molecule [e.g. the compound of formula I or II (R<3> is alkyl or phenyl; X is group of formula III, etc.), etc.], and (E) 30-90wt% inorganic filler (preferably silica or alumina).

Description

【発明の詳細な説明】 [発明の技術分野] 本発明は、密着性がよく耐湿性に浸れ、しかも半導体素
子ベレットに加わる応力の小さいことを特長とする半導
体などの封止用樹脂組成物にI!lツる。
Detailed Description of the Invention [Technical Field of the Invention] The present invention relates to a resin composition for encapsulating semiconductors, etc., which is characterized by good adhesion, moisture resistance, and low stress applied to semiconductor element pellets. I! l Tsuru.

[発明の技術的背景とその問題点] 近年、半導体集積回路の分野においては、高集積化およ
び高信頼性化に伴い、半導体素子ベレットの大型化並び
に高密度実装技術の開発が進められている。 そのため
、半導体封止用樹脂材料どしては、直接モールドしても
素子ペレットに加わる応力が小さいという特性が強く要
求され−いる。
[Technical background of the invention and its problems] In recent years, in the field of semiconductor integrated circuits, with the increase in integration and reliability, progress has been made in increasing the size of semiconductor element pellets and developing high-density packaging technology. . Therefore, there is a strong demand for resin materials for semiconductor encapsulation to have a property that the stress applied to the element pellet is small even when directly molded.

半導体封止用樹脂としては、エポキシ樹脂、ノボラック
型フェノール64m、無機質充填材を主成分とし、さら
に硬化促進剤、着色剤、離型剤を含むモールド樹脂が耐
湿性、成形性に凌れているため封止用樹脂の主流となっ
ている。
As a resin for semiconductor encapsulation, a molding resin whose main components are epoxy resin, novolac type phenol 64m, and inorganic filler, and also contains a curing accelerator, coloring agent, and mold release agent has superior moisture resistance and moldability. Therefore, it has become the mainstream sealing resin.

しかしながら、この系の封止用樹脂で半導体素74 [
−−ルド撲ると、樹脂の応力により、パッシベーション
膜(′)素子ペレットにクラックを生じたり、 i’8
 ft劣化(lb(の変動くτど)の原因となる欠点が
ある。 この傾向は、素子のペレットサイズが大きくな
るほど、また高密度実装化するほど顕菩に現れる。 こ
の対策として素子ペレットに加わる応力の小さい1tl
llt(低応力4!1脂)の開発が必要である。 封[
L用樹脂を低応力化する方法として、Jポヤシ樹脂、フ
ェノール樹脂を可どう化したり、lT塑剤の添加が考え
られる。 しかし、)Tノール樹脂を硬化剤とするエポ
キシ樹脂組成物では硬化樹脂のガラス転移点が降下し、
高温電気特性が低下づるために信頼性ト問題がある。 
また1合成ゴム等を添加して素子に加わる応力を小さく
し、パッシベーション膜のクラックや素子ベレツ]〜の
クシツクの発生を少なく改良したものもあるが、反対に
合成ゴ11を添加したことによって樹脂組成物の半導体
素子およびリードフレームとの密着性が低下し、耐7L
I11竹が悪くなり信頼性に劣るという欠点があつl、
−0 [発明の目的1 本発明は、上記の欠点に鑑みてなされたものであり、そ
の目的は、密着性がよく、耐?51竹に浸れ、しかも半
導体素子ベレッ1−に加わる応力の小さい封11用樹脂
組成物を提供しようとするものである。
However, with this type of sealing resin, the semiconductor element 74 [
--If you hit the passivation film (') element pellet with cracks due to the stress of the resin, i'8
There is a drawback that causes ft deterioration (lb (variation τ, etc.) 1tl with low stress
It is necessary to develop llt (low stress 4!1 fat). Seal [
Possible methods for reducing stress in the L resin include making J Poyashi resin and phenol resin more flexible, and adding LT plasticizer. However, in the case of epoxy resin compositions using T-Nol resin as a curing agent, the glass transition point of the cured resin decreases,
There are reliability problems due to the deterioration of high-temperature electrical characteristics.
There are also products that reduce the stress applied to the element by adding synthetic rubber 1 to reduce the occurrence of cracks in the passivation film and cracks in the element. The adhesion of the composition to the semiconductor element and lead frame decreases, and the resistance to 7L decreases.
I11 has the disadvantage that the bamboo deteriorates and is less reliable.
-0 [Objective of the Invention 1 The present invention has been made in view of the above-mentioned drawbacks, and its object is to provide good adhesion and high durability. It is an object of the present invention to provide a resin composition for sealing 11 which can be immersed in bamboo 51 and has less stress applied to semiconductor element bellet 1-.

[発明の概要1 本発明者は、上記の目的を達成リベく鋭意研究を重ねた
結果、(1)アルカリ土金属酸化物、とく2)分子内に
エポキシ基、アミムLカルボキシル基、ヒドロキシル基
、シアノ基のうちから選ばれた 1種又は2種以−ヒの
基を有するオルガノボリシロキナンを添加すると低応力
化の効果が大きいにもかかわらず、半導体素子およびリ
ードフレームとのV!!W性に優れ、上記目的を達成す
る封1L用樹脂組成物に好適していることを見いだした
ものである。
[Summary of the Invention 1] As a result of intensive research to achieve the above object, the present inventor has found that (1) an alkaline earth metal oxide, especially 2) an epoxy group, an Amim L carboxyl group, a hydroxyl group, Although the addition of organoborisilokinane having one or more groups selected from cyano groups has a great effect of reducing stress, the V! ! It has been found that it has excellent W properties and is suitable for a resin composition for a 1L seal that achieves the above objectives.

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、 (C)アルカリ土金属酸化物、 (1つ)分子内に」ボキシ呈、アミノ基、カルボキシル
基、ヒドロキシル基及びシアン基のうちから選ばれた1
種又は2伸以Fの基を有するオルガノボリシロキリンイ
5よび (F)無機τ1充填材 を必須成分とし、かつ樹脂組成物に対して前記(F>1
11ffi光j刊材を30〜90t’Q甲%含有させる
ことを持運とする封!L用樹脂組成物である。
That is, the present invention provides: (A) an epoxy resin, (B) a novolac type phenolic resin, (C) an alkaline earth metal oxide, (1) a molecule containing a "boxylated" amino group, a carboxyl group, a hydroxyl group, and a cyanide group. 1 selected from the group
Organoborisiloxane 5 and (F) inorganic τ1 filler having a species or 2 or more groups of F are essential components, and the above (F>1
A seal that is designed to contain 30 to 90 t'Q A% of 11ffi optical journal material! This is a resin composition for L.

本発明に用いる(△)1ボキシ樹脂は、その分子中にエ
ポキシ樹脂を少なくとも2個有する化合物である限り、
・分子構造、分子布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
スフェノール望の芳香族航、シクロヘ:を呼ン誘尊体等
の脂環族系、さらに次の一般式で示される1ボ1.ジノ
ボラック系等の樹脂が挙げられる。
As long as the (Δ)1 boxy resin used in the present invention is a compound having at least two epoxy resins in its molecule,
- There are no particular restrictions on the molecular structure, molecular cloth, etc., and a wide range of commonly used ones can be included. For example, aromatic compounds such as bisphenols, alicyclic systems such as derivatives of cyclohexane, and alicyclic systems such as derivatives of bisphenols, and 1. Examples include dinovolak-based resins.

(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 1種又は2種以上混合して用
いることができる。
(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.) These epoxy resins may be used alone or in combination of two or more. I can do it.

本発明に用いる(R3)ノボラック型71ノール樹脂と
しては、フェノール、アルキルフJノール等のフIノー
ル類とホルムアルデヒドあるいはパラホルムアルγヒト
を反応さVで17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る。
The (R3) novolak-type 71-nol resin used in the present invention includes novolak-type phenol resins which can be obtained by reacting formaldehyde or paraformal γ-human with phenols such as phenols and alkyl phenols, and modified resins thereof; Examples include epoxidized or butylated novolac type phenolic resins.

ノボラック型フェノール樹脂の配合〃1合は、前記(△
)エポキシ樹脂のエポキシ基(a)と、([3)ノ小ン
ツク型ノ1ノール樹脂のフェノール外水1’lQ草(b
)どのEル比(a、b)が0.1〜10の範囲ぐあるこ
とが望ましい。 モル比が0.1未讃もしくは10を珀
えると耐湿性、成形作業性J5よひ硬化1カのi(気持
+iが悪くな()いずれの場合も好tしく’Eい、 従
つC前記の範囲内に限定される。
The formulation of novolac type phenolic resin (1) is as described above (△
) Epoxy group (a) of epoxy resin and ([3) phenolic external water 1'lQ grass (b
) It is desirable that the E ratio (a, b) be in the range of 0.1 to 10. When the molar ratio is less than 0.1 or more than 10, moisture resistance, molding workability, J5, and hardening are achieved. limited within the above range.

本発明に用いる(C)アルカリ土金属酸化物とし′((
よ、ベリリウム、ングネシウム、カルシウム、ス1〜ロ
ンTウム、バリウムの酸化物が挙げられる。
(C) Alkaline earth metal oxide used in the present invention'((
Examples include oxides of beryllium, magnesium, calcium, sulfonium, and barium.

(l(木的にはr;a O,Ca O,、F3a O,
Ba 02、MqO1〜’I[+(つ、、Be Ol[
3e02等でこれらの)ら持にカルシウム、ングネシウ
ム、バリウム系の酸化物が好ましい。 酸化物の形状は
特に限「(よしないが分散性をよくりるため、0.01
〜3f1m(r扮未払が望ましい。 この配合…は0.
05−・3千生%が好十しく1.0,05屯Φ%未満で
は十〇/1密着付が1qられず、また3ffT弔%を超
えるとtan flit帽成物を構造する場合作業性、
流DJ性が悪くkり好、Lしくない、、 アルカリ上金
属酸化物を配合・(〈)こと(5,1つ(親水15が増
え、これらが金属類との密着性を向にさせるものと推測
される。
(l (treewise r; a O, Ca O,, F3a O,
Ba 02, MqO1~'I[+(tsu,, Be Ol[
In 3e02, etc., calcium, magnesium, and barium-based oxides are preferable. The shape of the oxide is particularly limited to 0.01
~3f1m (preferably unpaid. This combination... is 0.
05-3000% is preferable; if it is less than 1.0.05ton Φ%, 10/1 adhesion will not be achieved, and if it exceeds 3ffT%, workability will decrease when constructing a tan flit cap product. ,
Flow DJ performance is poor, K is not good, L is not good, Contains metal oxides on alkali (〈) (5, 1 (Hydrophilicity 15 increases, and these improve the adhesion with metals) It is assumed that.

本発明に用いる(D)分子内にエポキシ基、アミン基、
カルボキシル ノ基のうちから選ばれた 1種又は2種以上の基を有す
るオルガノポリシ[1キリンとしCは、ジメチルポリシ
ロキサンなどを基本骨格構造とするものである限り、分
子構造、分子量、粘度などに特に制限はない。 例えば
次の一般式で示されるオルガノポリシロキサンを挙げる
ことができる。
(D) used in the present invention, an epoxy group, an amine group,
Organopolysiloxane having one or more groups selected from carboxyl groups [1 Kirin and C is the molecular structure, molecular weight, viscosity, etc., as long as the basic skeleton structure is dimethylpolysiloxane etc. There are no particular restrictions. For example, organopolysiloxanes represented by the following general formula can be mentioned.

+R’−)−N+1,、    +R’+OH.   
 +R’+CN             +の内から
選ばれる 1種又は2種以上の官能基を示す。 R3は
アルキル基若しくはフェニル基を、R AtL+ OI
+ 、±,を、kは0又は 1以上の整数を、×、yは
 1以ヒの整数をイれぞれ表す) 本成分は(C)成分
による(グれた密着性を保持したまま、更に応力を低減
させる効果がある。
+R'-)-N+1,, +R'+OH.
Indicates one or more functional groups selected from +R'+CN +. R3 is an alkyl group or a phenyl group, R AtL+ OI
+, ±, k is an integer of 0 or 1 or more, x, y is an integer of 1 or more. , which has the effect of further reducing stress.

本発明に用いる(E)無機質充填材としては、シII/
J粉末、1ルミノー、三酸化アンチモン、タルク、Y 
R19 /Jルシウ11、チタンホワイト、クレー、ア
スベス1へ、マイカ、ベンガラ、ガラス繊維、炭素$1
1ff等が挙げられ、特にシリカ粉末又はアルミノが好
ましい。 照ぽ質充填材の配合割合は、樹脂組成物の3
0へ・90申吊%含有することが必要である。 30弔
量%未満では、耐湿性、低応力化に効IJ!なく、90
重量%を超えるどかさばりが大きくなり成彩性が悪く実
用に適さない。
As the inorganic filler (E) used in the present invention, Si II/
J powder, 1 Luminor, antimony trioxide, talc, Y
R19 /J Luciu 11, titanium white, clay, asbeth 1, mica, red iron, glass fiber, carbon $1
1ff, etc., and silica powder or alumino are particularly preferred. The blending ratio of the terophore filler is 3% of the resin composition.
It is necessary to contain 0 to 90%. If the weight is less than 30%, it is effective for moisture resistance and stress reduction. No, 90
It is unsuitable for practical use because it has a large bulk that exceeds the weight percentage, and the coloring property is poor.

本発明の封止用樹脂組成物は、(A>エポキシ樹脂、(
[3)ノボラック型フェノール樹脂、(C)゛l′lカ
ル1金属酸化物、([))分子内にエポキシ基、ノ2ミ
ノ早、カルボキシル シアノ草のうりから選ばれた1種又は2種以上の阜をイ
i ン+るAルがノポリシ11ヤリン、(E)無機質充
填材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.Fil
lアミド、エステル類,パラフィン類などの離型剤、塩
素化パラフィン、ブロム1−ルエン,ヘキサブロムベン
ゼン、三酸化アンチモンなどの難燃剤、カーボンブラッ
ク、ベンガラなどの着色剤、シランカップリング剤、神
々の硬化促進剤等を適宜添加配合してもよい。
The sealing resin composition of the present invention includes (A>epoxy resin, (
[3] Novolac type phenolic resin, (C) Cal 1 metal oxide, ([)) epoxy group in the molecule, one or two selected from No2MinoHari, Carboxyl Cyano Grass Uri (E) An inorganic filler is an essential component, but if necessary, for example, natural waxes, synthetic waxes, metal salts of straight chain fatty acids, etc. may be added. Fil
Mold release agents such as l amides, esters, paraffins, chlorinated paraffins, flame retardants such as bromo-1-luene, hexabromobenzene, antimony trioxide, colorants such as carbon black and red iron, silane coupling agents, gods A curing accelerator 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、合成ゴム又はその誘導体、オルガノ
ポリシロキサン、無機質充填材その他を配合しミキ1ナ
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、また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
とり。
A general method for preparing the sealing resin composition of the present invention as a molding material is to mix epoxy resin, novolac type phenol resin, synthetic rubber or its derivatives, organopolysiloxane, inorganic filler, etc. After sufficiently uniformly mixing the mixture using a roller or the like, the mixture is further melted and mixed using a heated roll or mixed using a kneader, etc., and then cooled and solidified and ground to an appropriate size to obtain a molding material.

ることができる。 そしてこの成形材料を電子部品ある
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さけることができる。
can be done. If this molding material is applied to seal, cover, insulate, etc. electronic or electrical components, excellent characteristics and reliability can be imparted.

[発明の効果1 本発明の月11−用樹脂組成物は、密着性がよく耐湿f
1に1坏れ、しかム半導体木了ベレットに加わる応力が
小さい!こめ、凸集積化に伴う大型ベレットや高密度実
装化した素子ベレットの封止用等に用いた場合、+分な
信頼性を1りることができる。
[Effect of the invention 1 The resin composition for use in the month 11 of the present invention has good adhesion and moisture resistance.
One-for-one, the stress applied to the semiconductor pellet is small! In addition, when used for sealing large pellets associated with convex integration or device pellets with high-density packaging, reliability can be significantly improved.

[発明の実施例J 本発明を実施例により1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。
[Example J of the Invention The present invention will be explained in detail with reference to Examples, but the present invention is not limited to the following Examples.

以l・実施例および比較例において、「%」とあるのは
1重量%」を意味する。
In the following Examples and Comparative Examples, "%" means 1% by weight.

実施例 1 クレゾールノボラックエポキシ樹脂(エポキシ当量21
5) 18%、ノボラック型フェノール樹脂()1ノー
ル当fit 107) 10%、酸化カルシウム1%、
カルボ−1シル基を有するジメチルポリシロキリン1%
、シリカ粉末69%、n級脂肪酸エステル1%を常温で
混合し、90〜95℃で混練して冷Wした1麦、粉砕し
て成形材料を得た。 得られた成形材料をタブレゾl−
化し、予熱してトランスファー成形で 170℃に加熱
した金型内に注入し硬化さけて成形品を得た。 この成
形品についでfjl M的特性、ガラス転移点、耐湿性
試験、濡寒昏ナイクル試験を行ったので第1表に示した
Example 1 Cresol novolak epoxy resin (epoxy equivalent weight 21
5) 18%, novolak type phenolic resin () fit per 1 mol 107) 10%, calcium oxide 1%,
1% dimethylpolysiloquiline with carbo-1 yl group
, 69% of silica powder, and 1% of n-class fatty acid ester were mixed at room temperature, kneaded at 90 to 95°C, cooled and crushed, and a molding material was obtained. The obtained molding material is tabreso l-
The molded product was preheated and poured into a mold heated to 170°C by transfer molding to avoid curing. This molded article was subjected to fjlM characteristics, glass transition point, moisture resistance test, and wet/cold Nicle test, which are shown in Table 1.

実施W42 クレゾールノボラックエポキシ樹脂(エポキシ1晴21
5) 17.5%、ノボラック型フェノール樹脂(フェ
ノール当量107) 10%、酸化マグネシウム0.5
%、ヒドロキシル基含有ジメチルポリシロキサン1%、
シリカ粉末69%、高級脂肪耐重ステル1%を実施例1
と同様に混合混練して成形材料を得た。 次いで同様に
成形材料を用いて成形品を得て、成形品に関し同じ特性
について試験をしたので第1表に示した。
Implementation W42 Cresol novolak epoxy resin (epoxy 1 fine 21
5) 17.5%, novolac type phenolic resin (phenol equivalent: 107) 10%, magnesium oxide 0.5
%, hydroxyl group-containing dimethylpolysiloxane 1%,
Example 1: 69% silica powder, 1% high-grade fat weight-resistant stellium
A molding material was obtained by mixing and kneading in the same manner as above. Next, a molded article was obtained using the same molding material, and the molded article was tested for the same characteristics, which are shown in Table 1.

比較例 1 クレゾールノボラックエポキシ樹脂(エポキシ当121
5) 18%、ノボラック型フェノール樹脂(フェノー
ル当fi +07) 10%、酸化カルシウム1%、シ
リカ粉末70%、高級脂肪酸エステル1%を実施例1と
同様に混合混練して成形材料を(9た。
Comparative Example 1 Cresol novolac epoxy resin (121% per epoxy
5) A molding material was prepared by mixing and kneading 18%, novolac type phenol resin (phenol equivalent fi +07), 1% calcium oxide, 70% silica powder, and 1% higher fatty acid ester in the same manner as in Example 1. .

次いぐ成形品を作り、この成形品に関して諸特性を試験
したので第1表に示した。
Next, a molded article was made, and various properties of this molded article were tested and are shown in Table 1.

比較例 2 クレゾールノボラックエポキシ樹脂(エポキシ当量21
5) 18%、ノボラック型フェノール樹脂(フェノー
ル当ffi 107) 10%、ヒドロキシル基金ず1
ジメ1ルボリシロ−1リン 1%、シリカ粉末lO%、
高級脂肪酸1スプル1%を実施例1と同様にして成形材
料、成形品を得て、次いで諸特性を試験したので第1表
に示した。
Comparative Example 2 Cresol novolak epoxy resin (epoxy equivalent: 21
5) 18%, novolac type phenolic resin (phenol ffi 107) 10%, hydroxyl foundation 1
Dimer 1 Rubori Shiro-1 Phosphorus 1%, Silica Powder 10%,
A molding material and a molded article were obtained using 1% sprue of higher fatty acids in the same manner as in Example 1, and then various properties were tested and are shown in Table 1.

第1表 *1;封止用樹脂組成物を用いて2木のアルミニウム配
線を有する電気部品を170℃で3分間トランスファー
成形し、ぞの侵180℃で8時開硬化させた。こうして
冑た月11−電気部品100個について、120℃の高
圧水蒸気中で15Vの電圧を加え耐湿性試験を行い、ア
ルミニウム腐食による50%の断線(不良発生)の起こ
る時間を評価した。
Table 1 *1: Using the sealing resin composition, an electric component having two aluminum wirings was transfer-molded at 170°C for 3 minutes, and then cured at 180°C with an opening at 8 o'clock. Thus, 100 electrical components were subjected to a moisture resistance test by applying a voltage of 15 V in high-pressure steam at 120° C., and the time required for 50% disconnection (defect occurrence) due to aluminum corrosion was evaluated.

*2;クラック数は、30x 25x 5nhaの成形
品のIt’(面に25x 25x 3msの銅板を埋め
込み、−40℃と200℃の恒温槽へ各30分間ずつ入
れ、、10リイクル< 1.)返した(春の(0(脂ク
ラックを謂 −1−t、  !、:。
*2; The number of cracks is the It' of a molded product of 30 x 25 x 5 nha (a copper plate of 25 x 25 x 3 ms is embedded in the surface, placed in a constant temperature bath of -40℃ and 200℃ for 30 minutes each, 10 recycles < 1.) Returned (spring's (0 (so-called greasy crack) -1-t, !,:.

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、 (C)アルカリ土金属酸化物、 (D)分子内にエポキシ基、アミノ基、カルボキシル基
、ヒドロキシル基及びシアノ基のうらから選ばれた1種
又は2種以上の基を有するオルガノポリシロキサンおよ
び (E)無機質充填材 を必須成分とし、かつ樹脂組成物に対して前記(E)無
機質充填材を30〜90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)とのモル比
(a/b)が0.1〜10の範囲内である特許請求の範
囲第1項記載の封止用樹脂組成物。
[Scope of Claims] 1 (A) Epoxy resin, (B) Novolak phenol resin, (C) Alkaline earth metal oxide, (D) Epoxy group, amino group, carboxyl group, hydroxyl group, and cyano group in the molecule An organopolysiloxane having one or more groups selected from the following and (E) an inorganic filler are essential components, and the amount of the (E) inorganic filler is 30 to 90% by weight based on the resin composition. % of the sealing resin composition. 2. Claim 1, wherein the molar ratio (a/b) between the epoxy group (a) of the epoxy resin and the phenolic hydroxyl group (b) of the novolac type phenol resin is within the range of 0.1 to 10. A resin composition for sealing.
JP669385A 1985-01-19 1985-01-19 Resin composition for sealing Pending JPS61166823A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP669385A JPS61166823A (en) 1985-01-19 1985-01-19 Resin composition for sealing

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP669385A JPS61166823A (en) 1985-01-19 1985-01-19 Resin composition for sealing

Publications (1)

Publication Number Publication Date
JPS61166823A true JPS61166823A (en) 1986-07-28

Family

ID=11645421

Family Applications (1)

Application Number Title Priority Date Filing Date
JP669385A Pending JPS61166823A (en) 1985-01-19 1985-01-19 Resin composition for sealing

Country Status (1)

Country Link
JP (1) JPS61166823A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63108021A (en) * 1986-10-24 1988-05-12 Hitachi Ltd Epoxy resin composition for semiconductor sealing and semiconductor device sealed therewith
JPS63202620A (en) * 1987-02-18 1988-08-22 Matsushita Electric Works Ltd Epoxy resin molding material
JPH01203423A (en) * 1988-02-08 1989-08-16 Matsushita Electric Works Ltd Epoxy resin molding material
JPH03157448A (en) * 1989-11-15 1991-07-05 Mitsubishi Electric Corp Epoxy resin composition for sealing semiconductor
JP2012007077A (en) * 2010-06-24 2012-01-12 Panasonic Electric Works Co Ltd Epoxy resin composition for sealing semiconductor and semiconductor device using the same

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56136816A (en) * 1980-03-31 1981-10-26 Shin Etsu Chem Co Ltd Epoxy resin composition
JPS5723625A (en) * 1980-07-17 1982-02-06 Toshiba Corp Epoxy resin composition and resin-sealed semiconductor device
JPS5869244A (en) * 1981-10-21 1983-04-25 Toray Silicone Co Ltd Epoxy resin composition for molding
JPS58174434A (en) * 1982-04-08 1983-10-13 Sumitomo Bakelite Co Ltd Epoxy resin molding material
JPS5933319A (en) * 1982-08-20 1984-02-23 Shin Etsu Chem Co Ltd Flame-retarding epoxy resin composition

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56136816A (en) * 1980-03-31 1981-10-26 Shin Etsu Chem Co Ltd Epoxy resin composition
JPS5723625A (en) * 1980-07-17 1982-02-06 Toshiba Corp Epoxy resin composition and resin-sealed semiconductor device
JPS5869244A (en) * 1981-10-21 1983-04-25 Toray Silicone Co Ltd Epoxy resin composition for molding
JPS58174434A (en) * 1982-04-08 1983-10-13 Sumitomo Bakelite Co Ltd Epoxy resin molding material
JPS5933319A (en) * 1982-08-20 1984-02-23 Shin Etsu Chem Co Ltd Flame-retarding epoxy resin composition

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63108021A (en) * 1986-10-24 1988-05-12 Hitachi Ltd Epoxy resin composition for semiconductor sealing and semiconductor device sealed therewith
JPS63202620A (en) * 1987-02-18 1988-08-22 Matsushita Electric Works Ltd Epoxy resin molding material
JPH01203423A (en) * 1988-02-08 1989-08-16 Matsushita Electric Works Ltd Epoxy resin molding material
JPH03157448A (en) * 1989-11-15 1991-07-05 Mitsubishi Electric Corp Epoxy resin composition for sealing semiconductor
JP2012007077A (en) * 2010-06-24 2012-01-12 Panasonic Electric Works Co Ltd Epoxy resin composition for sealing semiconductor and semiconductor device using the same

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