JPH05255479A - Epoxy resin composition and its cured product - Google Patents

Epoxy resin composition and its cured product

Info

Publication number
JPH05255479A
JPH05255479A JP8840792A JP8840792A JPH05255479A JP H05255479 A JPH05255479 A JP H05255479A JP 8840792 A JP8840792 A JP 8840792A JP 8840792 A JP8840792 A JP 8840792A JP H05255479 A JPH05255479 A JP H05255479A
Authority
JP
Japan
Prior art keywords
epoxy resin
resin composition
cured product
formula
epoxy compound
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.)
Granted
Application number
JP8840792A
Other languages
Japanese (ja)
Other versions
JP3204461B2 (en
Inventor
Yasumasa Akatsuka
泰昌 赤塚
Shigeru Mogi
繁 茂木
Hiromi Morita
博美 森田
Tomiyoshi Ishii
富好 石井
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.)
Nippon Kayaku Co Ltd
Original Assignee
Nippon Kayaku Co Ltd
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 Nippon Kayaku Co Ltd filed Critical Nippon Kayaku Co Ltd
Priority to JP08840792A priority Critical patent/JP3204461B2/en
Publication of JPH05255479A publication Critical patent/JPH05255479A/en
Application granted granted Critical
Publication of JP3204461B2 publication Critical patent/JP3204461B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime 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 subject composition containing a specific epoxy compound and a specific phenolic compound, having high heat-resistance and low water-absorption and useful as a sealing material, etc., for electric and electronic parts, etc. CONSTITUTION:The objective composition contains (A) an epoxy compound expressed by formula I (R1 to R3 are H, halogen, 1-4C alkyl or aryl) and (B) a phenolic compound expressed by formula II (R4 and R5 are H, halogen, 1-4C alkyl or aryl; (n) is 0-10). The amount of the component B used as a curing agent is preferably 0.5-1.5 equivalent based on 1 equivalent of the epoxy compound of the component A.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は耐熱性及び低吸水性に極
めて優れた硬化物を与える電気・電子部品材として有用
なエポキシ樹脂組成物及びその硬化物に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an epoxy resin composition useful as an electric / electronic component material which gives a cured product having excellent heat resistance and low water absorption and a cured product thereof.

【0002】[0002]

【従来の技術】従来、エポキシ樹脂はその優れた特性か
ら電気、電子用の部品材料として使用され、特に近年に
おいては、LSI,ICの封止剤、積層板などの電気・
電子部品材料として優れた硬化物を提供してきた。
2. Description of the Related Art Epoxy resin has been used as a material for electric and electronic parts because of its excellent characteristics.
We have provided excellent cured products as electronic component materials.

【0003】ところが最近ではLSIの表面実装が行わ
れており、半田浴中に直接浸漬される場合が増えてきて
いる。その際、封止剤は、200℃以上の高温にさらさ
れるため、封止剤中に吸湿していた水分が膨張し、封止
材にクラックが入るという問題がある。このため、エポ
キシ樹脂封止剤にはこうした高温に耐えうるだけの耐熱
性と、低吸水性が要求されてきた。
Recently, however, the surface mounting of LSIs has been carried out, and the number of cases where they are directly immersed in a solder bath is increasing. At that time, since the sealant is exposed to a high temperature of 200 ° C. or higher, there is a problem that the moisture absorbed in the sealant expands and the sealant cracks. Therefore, the epoxy resin sealant has been required to have heat resistance sufficient to withstand such high temperatures and low water absorption.

【0004】現状では、封止用のエポキシ樹脂としてo
−クレゾールノボラックのグリシジルエーテル、硬化剤
として、フェノールノボラックを用いる組合せが主流と
なってはいるものの今だ十分な諸特性を有するものは提
案されていない。
At present, as an epoxy resin for sealing,
-Although a combination of glycidyl ether of cresol novolac and phenol novolac as a curing agent has become the mainstream, one having sufficient various properties has not been proposed yet.

【0005】[0005]

【発明が解決しようとする課題】耐熱性と低吸水性の点
においてo−クレゾールノボラックのグリシジルエーテ
ルとフェノールノボラックの組合せからなる封止剤はバ
ランスは取れているものの、LSI実装技術の急速な進
歩には十分対応しきれていないのが現状である。
In view of heat resistance and low water absorption, the encapsulant composed of a combination of glycidyl ether of o-cresol novolac and phenol novolac is well balanced, but rapid progress in LSI packaging technology. The current situation is that we have not fully dealt with.

【0006】例えば吸水性を改善するために炭素数の多
いアルキル基で置換された置換フェノールノボラックの
グリシジルエーテルを用いた場合、低吸水性が実現され
る反面、耐熱性や硬化性が低下する。
For example, when a glycidyl ether of a substituted phenol novolac substituted with an alkyl group having a large number of carbon atoms is used to improve water absorption, low water absorption is realized, but heat resistance and curability are deteriorated.

【0007】これら相反する要求特性を同時に満足させ
るためにはエポキシ樹脂あるいは硬化剤を単独で改良す
るだけではなく両者の組合せも考慮に入れる必要がある
のではないかという考え方に基づき、鋭意検討を重ねた
結果、本発明に至ったのである。
In order to satisfy these contradictory required properties at the same time, it is necessary to consider not only the epoxy resin or the curing agent alone, but also the combination of the two. As a result of the repeated stacking, the present invention was achieved.

【0008】[0008]

【課題を解決するための手段】本発明は、(1)(a)
下記式(1)で表されるエポキシ化合物
The present invention provides (1) (a)
Epoxy compound represented by the following formula (1)

【0009】[0009]

【化3】 [Chemical 3]

【0010】(式中、R1 ,R2 ,R3 はそれぞれ独立
して水素原子、ハロゲン原子、炭素数1〜4のアルキル
基、またはアリール基を示す。)及び(b)下記式
(2)で表されるフェノール類化合物、
(Wherein R 1 , R 2 and R 3 each independently represent a hydrogen atom, a halogen atom, an alkyl group having 1 to 4 carbon atoms, or an aryl group) and (b) the following formula (2) ) A phenolic compound represented by

【0011】[0011]

【化4】 [Chemical 4]

【0012】(式中、R4 ,R5 はそれぞれ独立して、
水素原子、ハロゲン原子、炭素数1〜4のアルキル基、
またはアリール基を、nは0から10までの値好ましく
は0から6までの値を表す。)を含有することを特徴と
するエポキシ樹脂組成物、
(In the formula, R 4 and R 5 are each independently
Hydrogen atom, halogen atom, alkyl group having 1 to 4 carbon atoms,
Alternatively, an aryl group and n represents a value of 0 to 10, preferably a value of 0 to 6. ) Is contained in the epoxy resin composition,

【0013】(2)(a)のエポキシ化合物1当量に対
して(b)のフェノール類化合物を硬化剤として0.5
〜1.5当量含有する上記(1)記載のエポキシ樹脂組
成物、(3)上記(1)または(2)記載のエポキシ樹
脂組成物の硬化物に関するものである。
(2) 0.5 equivalent of the phenol compound of (b) as a curing agent to 1 equivalent of the epoxy compound of (a)
The present invention relates to the epoxy resin composition described in (1) above, which is contained in an amount of from 1.5 to 1.5 equivalents, and (3) the cured product of the epoxy resin composition described in (1) or (2) above.

【0014】成分(a)である式(1)で表されるエポ
キシ化合物は本発明のエポキシ樹脂組成物の硬化物に対
し高い耐熱性を付与する。又式(1)のエポキシ化合物
はナフタレン環のように平面的な構造を有しているた
め、分子間のパッキングが良好であり硬化物において低
吸水性をも付与する。成分(b)である式(2)で表さ
れるフェノール類化合物はその硬化物に対して耐熱性を
保持しながら、低吸水性をも付与する。
The epoxy compound represented by the formula (1), which is the component (a), imparts high heat resistance to the cured product of the epoxy resin composition of the present invention. Further, since the epoxy compound of the formula (1) has a planar structure like a naphthalene ring, it has good intermolecular packing and imparts low water absorption to the cured product. The phenolic compound represented by the formula (2), which is the component (b), imparts low water absorption to the cured product while maintaining heat resistance.

【0015】前記式(1)及び(2)のR1 〜R5 にお
いて、ハロゲン原子としては塩素原子、臭素原子などが
挙げられ、炭素数1〜4のアルキル基としてはメチル
基、エチル基、t−ブチル基などが挙げられ、アリール
基としてはフェニル基、ナフチル基などが挙げられる。
In R 1 to R 5 of the above formulas (1) and (2), examples of the halogen atom include chlorine atom and bromine atom, and examples of the alkyl group having 1 to 4 carbon atoms include methyl group, ethyl group, Examples thereof include t-butyl group, and examples of the aryl group include phenyl group and naphthyl group.

【0016】本発明のエポキシ樹脂組成物は、必要に応
じ硬化促進剤を含むことができ、硬化促進剤としては、
2−メチルイミダゾール、2−エチルイミダゾール等の
イミダゾール系化合物、2−(ジメチルアミノメチル)
フェノール等の第3級アミン系化合物、トリフェニルホ
スフィンなど、公知の種々の硬化促進剤が挙げられ特に
限定されるものではない。これらは単独で用いてもよ
く、2種以上を併用してもよい。硬化促進剤は、(a)
のエポキシ化合物100重量部に対して0.01〜15
重量部用いるのが好ましく、特に0.1〜10重量部用
いるのが用いるのが好ましい。
The epoxy resin composition of the present invention may contain a curing accelerator, if necessary.
Imidazole compounds such as 2-methylimidazole and 2-ethylimidazole, 2- (dimethylaminomethyl)
Various known curing accelerators such as tertiary amine compounds such as phenol, triphenylphosphine, etc. may be mentioned and are not particularly limited. These may be used alone or in combination of two or more. The curing accelerator is (a)
0.01 to 15 per 100 parts by weight of the epoxy compound
It is preferable to use parts by weight, particularly preferably 0.1 to 10 parts by weight.

【0017】本発明のエポキシ樹脂組成物には、更に必
要に応じて公知の添加剤を配合することが出来る。添加
剤としては、例えば、シリカ、アルミナ、タルク、ガラ
ス繊維等の無機充填剤、シランカップリング剤のような
充填剤の表面処理剤、離型剤、顔料等が挙げられる。
The epoxy resin composition of the present invention may further contain known additives, if necessary. Examples of the additives include inorganic fillers such as silica, alumina, talc and glass fibers, surface treatment agents for fillers such as silane coupling agents, release agents, pigments and the like.

【0018】本発明のエポキシ樹脂組成物は、各成分を
均一に混合することにより得られ、通常130〜170
℃の温度で30〜300秒の範囲で予備硬化し、更に、
150〜200℃の温度で2〜10時間,後硬化するこ
とにより充分な硬化反応が進行し、本発明の硬化物が得
られる。又、エポキシ樹脂組成物の成分を溶剤等に均一
に分散または溶解させ、溶剤を除去し硬化させることも
できる。
The epoxy resin composition of the present invention is obtained by uniformly mixing the components, and is usually 130 to 170.
Pre-cure in the range of 30-300 seconds at a temperature of ℃,
By post-curing at a temperature of 150 to 200 ° C. for 2 to 10 hours, a sufficient curing reaction proceeds to obtain the cured product of the present invention. It is also possible to uniformly disperse or dissolve the components of the epoxy resin composition in a solvent or the like, remove the solvent, and cure.

【0019】こうして得られる硬化物は高い耐熱性を保
持しているため、本発明のエポキシ樹脂組成物は、耐熱
性の要求される広範な分野で用いることが出来る。具体
的には、絶縁材料、積層板、封止材料等あらゆる電気・
電子材料として有用である。又、成形材料、複合材料の
他、塗料材料等の分野にも用いることが出来る。
Since the cured product thus obtained retains high heat resistance, the epoxy resin composition of the present invention can be used in a wide range of fields where heat resistance is required. Specifically, all kinds of electrical materials such as insulating materials, laminated boards, sealing materials, etc.
It is useful as an electronic material. In addition to molding materials and composite materials, they can also be used in fields such as coating materials.

【0020】[0020]

【実施例】以下本発明を実施例で説明する。尚、本発明
はこれら実施例に限定されるものではない。
EXAMPLES The present invention will be described below with reference to examples. The present invention is not limited to these examples.

【0021】実施例1〜5、比較例1 エポキシ化合物(a)として下記式(3)で表されるエ
ポキシ化合物(エポキシ当量212g/eq、軟化点7
1℃)を、
Examples 1 to 5 and Comparative Example 1 An epoxy compound represented by the following formula (3) as the epoxy compound (a) (epoxy equivalent 212 g / eq, softening point 7)
1 ° C)

【0022】[0022]

【化5】 [Chemical 5]

【0023】硬化剤(b)として下記式(4)で表され
るフェノール類化合物(水酸基当量140g/eq)
を、
As the curing agent (b), a phenol compound represented by the following formula (4) (hydroxyl group equivalent: 140 g / eq)
To

【0024】[0024]

【化6】 [Chemical 6]

【0025】(式中、nの値は1.9(平均値)であ
る) 又、比較例においては従来使用のオルソクレゾールノボ
ラックエポキシ樹脂(EOCN1020、エポキシ当量
200g/eq、軟化点67℃、日本化薬(株)製)に
対し硬化剤として式(4)で表されるフェノール類化合
物を用い、これらを硬化促進剤と表1に示す割合で混合
し、エポキシ樹脂組成物を得た。尚、硬化促進剤として
トリフェニルホスフィンを用いた。各成分を混合して得
たエポキシ樹脂組成物は70〜80℃で15分間ロール
混練、冷却、粉砕し、タブレット化し、さらにトランス
ファー成形機により成形後、ポストキュアを行って硬化
物を得、この硬化物のガラス転移温度及び吸水率を測定
した。
(In the formula, the value of n is 1.9 (average value)) Also, in the comparative example, the conventionally used orthocresol novolac epoxy resin (EOCN1020, epoxy equivalent 200 g / eq, softening point 67 ° C., Japan A phenol compound represented by the formula (4) was used as a curing agent for Kayaku Co., Ltd., and these were mixed with a curing accelerator at a ratio shown in Table 1 to obtain an epoxy resin composition. Triphenylphosphine was used as a curing accelerator. The epoxy resin composition obtained by mixing the respective components is roll-kneaded at 70 to 80 ° C. for 15 minutes, cooled, pulverized, tabletted, further molded by a transfer molding machine, and post-cured to obtain a cured product. The glass transition temperature and water absorption of the cured product were measured.

【0026】測定結果を表1に示す。尚、ガラス転移温
度及び吸水率の測定条件、トランスファーの成形条件及
びポストキュアの条件は次の通りである。 ガラス転移温度 熱機械測定装置(TMA):真空理工(株)製 TM−
7000 昇温速度:2℃/min 吸水率 試験片(硬化物):直径 50mm 厚さ 3mm 円盤 100℃の水中で24時間煮沸した後の重量増加量(重
量%)
The measurement results are shown in Table 1. The glass transition temperature and water absorption measurement conditions, transfer molding conditions, and post cure conditions are as follows. Glass transition temperature thermomechanical measuring device (TMA): TM- manufactured by Vacuum Riko Co., Ltd.
7000 Temperature rising rate: 2 ° C / min Water absorption rate Test piece (cured product): Diameter 50 mm Thickness 3 mm Disc Weight increase after boiling in 100 ° C water for 24 hours (% by weight)

【0027】トランスファー成形条件 温度:150℃ 成形圧力:50kg/cm2 時間:3分 ポストキュアの条件 温度:180℃ 時間:8時間Transfer molding conditions Temperature: 150 ° C. Molding pressure: 50 kg / cm 2 hours: 3 minutes Post-cure conditions Temperature: 180 ° C. Time: 8 hours

【0028】尚、表1において、各成分の欄の数値は重
量部を表す。
In Table 1, the numerical values in the column of each component represent parts by weight.

【0029】 表 1 実 施 例 比較例 1 2 3 4 5 1 エポキシ化合物(a) 100 100 100 100 100 オルソクレゾール ノボラック 100 エポキシ樹脂 硬化剤(b) 40 53 66 79 92 70 硬化促進剤 1 1 1 1 1 1 ガラス転移温度(℃) 152 155 157 154 153 154 吸水率(%) 0.67 0.68 0.67 0.64 0.62 1.05 Table 1 Actual Example Comparative Example 1 2 3 4 5 1 Epoxy compound (a) 100 100 100 100 100 Orthocresol Novolac 100 Epoxy resin Curing agent (b) 40 53 66 79 92 70 Curing accelerator 1 1 1 1 1 1 Glass transition temperature (℃) 152 155 157 154 153 154 Water absorption (%) 0.67 0.68 0.67 0.64 0.62 1.05

【0024】[0024]

【発明の効果】本発明のエポキシ樹脂組成物の硬化物は
高耐熱性でかつ低吸水性であり、封止剤など種々の用途
に有用である。本発明のエポキシ樹脂組成物で用いる成
分(a)のエポキシ化合物及び成分(b)のフェノール
類化合物はそれぞれ耐熱性、吸水性の面において従来の
フェノールノボラック型のエポキシ樹脂、及び硬化剤と
してのフェノールノボラックに比べて優れた性質を有し
ており、バラスンのとれた特性を有する硬化物を提供す
ることが可能である。
The cured product of the epoxy resin composition of the present invention has high heat resistance and low water absorption, and is useful for various uses such as a sealant. The epoxy compound of component (a) and the phenol compound of component (b) used in the epoxy resin composition of the present invention are the conventional phenol novolac type epoxy resin and phenol as a curing agent in terms of heat resistance and water absorption. It is possible to provide a cured product having excellent properties as compared with novolac and having excellent properties.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】(a)下記式(1)で表されるエポキシ化
合物 【化1】 (式中、R1 ,R2 ,R3 はそれぞれ独立して水素原
子、ハロゲン原子、炭素数1〜4のアルキル基、または
アリール基を示す。)及び(b)下記式(2)で表され
るフェノール類化合物 【化2】 (式中、R4 ,R5 はそれぞれ独立して水素原子、ハロ
ゲン原子、炭素数1〜4のアルキル基、またはアリール
基を、nは0から10までの値を表す。)を含有するこ
とを特徴とするエポキシ樹脂組成物。
1. An epoxy compound represented by the following formula (1): (In the formula, R 1 , R 2 , and R 3 each independently represent a hydrogen atom, a halogen atom, an alkyl group having 1 to 4 carbon atoms, or an aryl group.) And (b) represented by the following formula (2). Phenol compounds (Wherein R 4 and R 5 each independently represent a hydrogen atom, a halogen atom, an alkyl group having 1 to 4 carbon atoms, or an aryl group, and n represents a value from 0 to 10). An epoxy resin composition characterized by:
【請求項2】(a)のエポキシ化合物1当量に対して
(b)のフェノール類化合物を硬化剤として0.5〜
1.5当量含有する請求項1記載のエポキシ樹脂組成
物。
2. A phenol compound of (b) is used as a curing agent in an amount of 0.5 to 1 equivalent of the epoxy compound of (a).
The epoxy resin composition according to claim 1, which contains 1.5 equivalents.
【請求項3】請求項1または2記載のエポキシ樹脂組成
物の硬化物。
3. A cured product of the epoxy resin composition according to claim 1.
JP08840792A 1992-03-13 1992-03-13 Epoxy resin composition and cured product thereof Expired - Lifetime JP3204461B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP08840792A JP3204461B2 (en) 1992-03-13 1992-03-13 Epoxy resin composition and cured product thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP08840792A JP3204461B2 (en) 1992-03-13 1992-03-13 Epoxy resin composition and cured product thereof

Publications (2)

Publication Number Publication Date
JPH05255479A true JPH05255479A (en) 1993-10-05
JP3204461B2 JP3204461B2 (en) 2001-09-04

Family

ID=13941948

Family Applications (1)

Application Number Title Priority Date Filing Date
JP08840792A Expired - Lifetime JP3204461B2 (en) 1992-03-13 1992-03-13 Epoxy resin composition and cured product thereof

Country Status (1)

Country Link
JP (1) JP3204461B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI415230B (en) * 2005-04-25 2013-11-11 Shinetsu Chemical Co Epoxy resin composition for semiconductor sealing and semiconductor device

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI415230B (en) * 2005-04-25 2013-11-11 Shinetsu Chemical Co Epoxy resin composition for semiconductor sealing and semiconductor device

Also Published As

Publication number Publication date
JP3204461B2 (en) 2001-09-04

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