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JPH05166974A - Epoxy resin composition - Google Patents

Epoxy resin composition

Info

Publication number
JPH05166974A
JPH05166974A JP32927791A JP32927791A JPH05166974A JP H05166974 A JPH05166974 A JP H05166974A JP 32927791 A JP32927791 A JP 32927791A JP 32927791 A JP32927791 A JP 32927791A JP H05166974 A JPH05166974 A JP H05166974A
Authority
JP
Japan
Prior art keywords
epoxy resin
resin composition
weight
formula
hardening agent
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
JP32927791A
Other languages
Japanese (ja)
Other versions
JP2963260B2 (en
Inventor
Masatoyo Tomokuni
勝豊 友囜
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.)
Sumitomo Bakelite Co Ltd
Original Assignee
Sumitomo Bakelite 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 Sumitomo Bakelite Co Ltd filed Critical Sumitomo Bakelite Co Ltd
Priority to JP32927791A priority Critical patent/JP2963260B2/en
Publication of JPH05166974A publication Critical patent/JPH05166974A/en
Application granted granted Critical
Publication of JP2963260B2 publication Critical patent/JP2963260B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related 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 enable epoxy resin composition to be enhanced in soldering heat resistance at soldering without deteriorating it in moldability and reliability by a method wherein specific epoxy resin, specific phenolic resin hardening agent, inorganic filler, and hardening accelerator are made to serve as essential ingredients of epoxy resin composition. CONSTITUTION:Epoxy resin which contains 30-100% copolycondensation novolac epoxy resin composed of O-cresol represented by a formula I and beta-naphthol by weight out of total epoxy resin is made to serve as a first component. Hardening agent which contains 30-100% phenolic resin hardening agent represented by a formula II by weight out of total hardening agent is made to serve as a second component. In the formulas I and II, a letter n denotes 1-6. In the formula II, R1 and R2 denote the same or a different atom or a group selected from hydrogen, halogen, a low class alkyl Furthermore, inorganic filler and hardening group. as essential ingredients. By this setup, a resin composition excellent in heat resistance and flexibility and low in water absorption properties can be obtained.

Description

【発明の詳现な説明】Detailed Description of the Invention

【】[0001]

【産業䞊の利甚分野】本発明は、耐半田ストレス性に優
れた半導䜓封止甚゚ポキシ暹脂組成物に関するものであ
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an epoxy resin composition for semiconductor encapsulation which is excellent in solder stress resistance.

【】[0002]

【埓来の技術】高集積デバむスは、そのほずんどが
信頌性、コスト及び量産性に優れる゚ポキシ暹脂封止材
料による暹脂封止方匏により封止されおいる。゚ポキシ
暹脂封止材料ずしおは、耐熱性、耐湿性、成圢性に優れ
たオル゜クレゟヌルノボラック゚ポキシ暹脂ずノボラッ
ク型フェノヌル暹脂で構成される暹脂組成物が甚いられ
おいる。しかし、近幎の高集積化、倚機胜化に䌎ない、
高集積パッケヌゞは、玠子の倧型化、実装合理化に
䌎うパッケヌゞの小型化、薄圢化の傟向が匷く、埓来の
タむプから、小型、薄型の、、
、タむプの衚面実装型パッケヌゞぞ急速に移
行しおいる。
2. Description of the Related Art Most highly integrated IC devices are encapsulated by a resin encapsulation method using an epoxy resin encapsulating material which is excellent in reliability, cost and mass productivity. As the epoxy resin encapsulating material, a resin composition composed of an orthocresol novolac epoxy resin and a novolac type phenol resin, which are excellent in heat resistance, moisture resistance and moldability, is used. However, with the recent high integration and multi-functionalization,
Highly integrated IC packages have a strong tendency to be smaller and thinner due to the larger size of devices and the rationalization of mounting. Compared to the conventional DIP type, small and thin SOJs, SOPs, and QFs are used.
P and TSOP type surface mount packages are rapidly shifting.

【】このこずは、埓来のタむプず違い半
田付け時にパッケヌゞそのものが〜℃の高
枩にさらされるこずずなり、倧型チップを小型で薄いパ
ッケヌゞに封入した衚面実装タむプのパッケヌゞは倧き
な応力を受け、パッケヌゞ暹脂のクラック、チップ界面
の剥離を匕き起こし、パッケヌゞの信頌性に臎呜的
な問題ずなっおいる。これらの衚面実装型パッケヌゞを
封止するのに適した信頌性の高い封止甚暹脂組成物が望
たれおいる。
This means that, unlike the conventional DIP type, the package itself is exposed to a high temperature of 215 to 260 ° C. at the time of soldering, and the surface mount type package in which a large chip is enclosed in a small and thin package exerts a large stress. This causes cracking of the package resin and peeling of the chip interface, which is a fatal problem in the reliability of the IC package. A highly reliable encapsulating resin composition suitable for encapsulating these surface mount packages is desired.

【】これらの問題を解決するために半田付け時
の熱衝撃を緩和する目的で、熱可塑性オリゎマヌの添加
特開昭−号公報や各皮シリコヌン
化合物の添加特開昭−号公報、
−号公報、−号公報、
曎にはシリコヌン倉性特開昭−号公
報などの手法で察凊しおいるがいずれも半田付け時に
パッケヌゞにクラックが生じおしたい信頌性の優れた半
導䜓封止甚゚ポキシ暹脂組成物を埗るたでには至らなか
った。
In order to alleviate the thermal shock during soldering in order to solve these problems, addition of a thermoplastic oligomer (JP-A-62-115849) and addition of various silicone compounds (JP-A-62-158). No. 115850, 62
-116654, 62-128162),
Furthermore, methods such as silicone modification (Japanese Patent Laid-Open No. 62-136860) are used, but in all cases cracks occur in the package during soldering, and a highly reliable epoxy resin composition for semiconductor encapsulation is obtained. It didn't reach.

【】䞀方、半田付け時の耐熱ストレス性぀たり
耐半田ストレス性に優れた半導䜓封止甚゚ポキシ暹脂組
成物を埗るために、暹脂系ずしおビフェニル型゚ポキシ
暹脂の䜿甚特開昭−号公報等が、怜
蚎されおきたがビフェニル型゚ポキシ暹脂の䜿甚により
リヌドフレヌムずの密着性及び䜎吞氎性が向䞊し、耐半
田ストレス性の向䞊、特にクラック発生が䜎枛するが、
耐熱性が劣るため特に℃以䞊のような高枩では耐
半田ストレス性が䞍十分である。
On the other hand, in order to obtain a semiconductor encapsulating epoxy resin composition having excellent heat stress resistance during soldering, that is, solder stress resistance, use of a biphenyl type epoxy resin as a resin system (Japanese Patent Laid-Open No. 64-65116). Gazette) has been studied, but the use of a biphenyl type epoxy resin improves the adhesion to the lead frame and the low water absorption, improves the solder stress resistance, and particularly reduces the occurrence of cracks.
Since the heat resistance is poor, the solder stress resistance is insufficient especially at a high temperature of 250 ° C. or higher.

【】[0006]

【発明が解決しようずする課題】本発明は、成圢性およ
び信頌性を劣化させるこずなく半田付け時の半田耐熱性
に優れた半導䜓封止甚゚ポキシ暹脂組成物を提䟛するも
のである。
SUMMARY OF THE INVENTION The present invention provides an epoxy resin composition for semiconductor encapsulation which is excellent in solder heat resistance during soldering without deteriorating moldability and reliability.

【】[0007]

【課題を解決するための手段】本発明は䞋蚘匏
で瀺されるオル゜クレゟヌルずβ−ナフトヌルの
共瞮合ノボラック゚ポキシ暹脂を総゚ポキシ暹脂量の
〜重量含む゚ポキシ暹脂、
The present invention comprises (A) a co-condensed novolak epoxy resin of orthocresol and β-naphthol represented by the following formula (1) in a total epoxy resin amount of 3: 1.
Epoxy resin containing 0 to 100% by weight,

【】[0008]

【化】 〜[Chemical 3] (N = 1 to 6)

【】䞋蚘匏で瀺されるフェノヌル
暹脂硬化剀を総硬化剀量に察しお〜重量含
む硬化剀、
(B) A curing agent containing a phenol resin curing agent represented by the following formula (2) in an amount of 30 to 100% by weight based on the total amount of the curing agent,

【】[0010]

【化】 [Chemical 4]

【】匏䞭の1 、2 は氎玠、ハロゲン、䜎
玚アルキル基の䞭から遞択される同䞀もしくは異なる原
子たたは基、〜 無機質充填材及び 硬化促進剀 を必須成分ずする半導䜓封止甚゚ポキシ暹脂組成物で、
埓来の゚ポキシ暹脂組成物に比べ非垞に優れた耐半田耐
熱性を有するものである。
(Wherein R 1 and R 2 are the same or different atoms or groups selected from hydrogen, halogen and lower alkyl groups, n = 1 to 6) (C) inorganic filler and (D) curing An epoxy resin composition for semiconductor encapsulation containing an accelerator as an essential component,
It has extremely excellent solder heat resistance as compared with conventional epoxy resin compositions.

【】本発明に甚いるオル゜クレゟヌルずβ−ナ
フトヌルの共瞮合ノボラック゚ポキシ暹脂は、オル゜ク
レゟヌルずβ−ナフトヌルをホルムアルデヒドより共瞮
合されたノボラック暹脂の゚ポキシ化物であり、その共
瞮合時のβ−ナフトヌル量は重量以䞊が望たし
く、匏の構造を䞻ずする化合物である。曎には
〜で、を越えるず成圢時の流動性に劣る。匏
は、䜎吞氎性に優れ、暹脂の線膚匵係数が小さ
く、成圢時の離型性に優れるずいう特城を有し、半田付
け時のハンダ耐熱性に良奜な結果を瀺す。このオル゜ク
レゟヌルずβ−ナフトヌル共瞮合ノボラック゚ポキシ暹
脂の䜿甚量は、これを調節するこずにより半田耐熱性を
最倧限に匕き出すこずができる。
The co-condensed novolak epoxy resin of orthocresol and β-naphthol used in the present invention is an epoxidized novolak resin obtained by co-condensing orthocresol and β-naphthol from formaldehyde, and β-naphthol at the time of the co-condensation thereof. The amount is preferably 50% by weight or more, and the compound mainly has the structure of formula (1). Further, n is 1 to 6, and if it exceeds 6, the fluidity at the time of molding is poor. Formula (1) has the characteristics of excellent low water absorption, a small linear expansion coefficient of the resin, and excellent releasability at the time of molding, and shows good results for solder heat resistance during soldering. By adjusting the amounts of the orthocresol and β-naphthol co-condensed novolac epoxy resin to be used, solder heat resistance can be maximized.

【】半田耐熱性の効果をだすためにはオル゜ク
レゟヌルずβ−ナフトヌル共瞮合ノボラック゚ポキシ暹
脂を総゚ポキシ暹脂量の重量以䞊奜たしくは
重量以䞊の䜿甚が望たしい。重量未満では、䜎
吞氎性、䜎線膚匵係数が充分に埗られず、半田耐熱性が
䞍充分である。オル゜クレゟヌルずβ−ナフトヌル共瞮
合ノボラック゚ポキシ暹脂以倖の他の゚ポキシ暹脂を䜵
甚する堎合、甚いる゚ポキシ暹脂ずは、゚ポキシ基を有
するポリマヌ党般をいう。たずえばビスフェノヌル型゚
ポキシ暹脂、クレゟヌルノボラック型゚ポキシ暹脂、ビ
フェニル型゚ポキシ暹脂、フェノヌルノボラック型゚ポ
キシ暹脂及びトリフェノヌルメタン型゚ポキシ暹脂、ア
ルキル倉性トリフェノヌルメタン型゚ポキシ暹脂等の
官胜型゚ポキシ暹脂、トリアゞン栞含有゚ポキシ暹脂等
のこずをいう。
In order to obtain the effect of solder heat resistance, orthocresol and β-naphthol co-condensed novolac epoxy resin are contained in an amount of 30% by weight or more, preferably 60% by weight or more of the total amount of epoxy resin.
It is desirable to use more than weight%. If it is less than 30% by weight, low water absorption and low linear expansion coefficient cannot be sufficiently obtained, and solder heat resistance is insufficient. When orthocresol and an epoxy resin other than the β-naphthol co-condensed novolac epoxy resin are used in combination, the epoxy resin to be used refers to all polymers having an epoxy group. For example, bisphenol type epoxy resin, cresol novolac type epoxy resin, biphenyl type epoxy resin, phenol novolac type epoxy resin and triphenol methane type epoxy resin, alkyl modified triphenol methane type epoxy resin, etc.
Functional epoxy resin, triazine nucleus-containing epoxy resin and the like.

【】匏で瀺されるフェノヌル暹脂硬化剀
は骚栌䞭のパラキシレンを倉性したものである。匏䞭の
は〜で、1 、2 は氎玠、ハロゲン、䜎玚アル
キル基の䞭から遞択される同䞀もしくは異なる原子たた
は基である。これらの䞭で、がを越えるず成圢時の
流動性に劣る。䜎玚アルキル基は炭玠が〜で、を
越えるず、成圢時の流動性が劣る。1、2ずしはそれ
ぞれ氎玠原子が奜たしい。特城ずしおはガラス転移枩床
以䞊での匟性率が䜎く、半田付け時の内郚応力が䜎い。
たた、チップ及びリヌドフレヌムずの密着性及び䜎吞氎
性に優れるなどの特城を有するこずから耐半田ストレス
性に良奜な結果を瀺す。このフェノヌル暹脂硬化剀の䜿
甚量は、党硬化剀量に察しお重量以䞊が奜たし
く、曎に奜たしくは重量以䞊の䜿甚が望たしい。
重量未満だず、リヌドフレヌムずの密着性及び䜎
吞氎性が向䞊せず、耐半田ストレス性が䞍充分である。
The phenol resin curing agent represented by the formula (2) is a modification of para-xylene in the skeleton. In the formula, n is 1 to 6, and R 1 and R 2 are the same or different atoms or groups selected from hydrogen, halogen and lower alkyl groups. Among these, when n exceeds 6, the fluidity during molding is poor. The lower alkyl group has 1 to 4 carbon atoms, and when it exceeds 4, the fluidity at the time of molding becomes poor. Each of R 1 and R 2 is preferably a hydrogen atom. It features low elastic modulus above glass transition temperature and low internal stress during soldering.
Further, since it has characteristics such as excellent adhesion to the chip and the lead frame and low water absorption, it shows good results in resistance to solder stress. The amount of the phenol resin curing agent used is preferably 30% by weight or more, more preferably 60% by weight or more, based on the total amount of the curing agent.
If it is less than 30% by weight, the adhesion to the lead frame and the low water absorption will not be improved, and the solder stress resistance will be insufficient.

【】匏で瀺されるフェノヌル暹脂硬化剀
以倖に他のフェノヌル暹脂硬化剀を䜵甚する堎合、甚い
るフェノヌル暹脂硬化剀ずはフェノヌル性氎酞基を有す
るポリマヌ党般をいう。䟋えば、䞀般にフェノヌルノボ
ラック暹脂、クレゟヌルノボラック暹脂、ゞシクロペン
タゞ゚ン倉性フェノヌル暹脂、ゞシクロペンタゞ゚ン倉
性フェノヌル暹脂ずフェノヌルノボラック及びクレゟヌ
ルノボラック暹脂ずの共瞮合物、パラキシレン倉性フェ
ノヌル暹脂等を甚いるこずができる。
When another phenol resin curing agent is used in combination with the phenol resin curing agent represented by the formula (2), the phenol resin curing agent used means all polymers having a phenolic hydroxyl group. For example, generally, phenol novolac resin, cresol novolac resin, dicyclopentadiene modified phenol resin, co-condensation product of dicyclopentadiene modified phenol resin and phenol novolac or cresol novolac resin, paraxylene modified phenol resin and the like can be used.

【】本発明で甚いる無機質充填材ずしおは、溶
融シリカ粉末、球状シリカ粉末、結晶シリカ粉末、二次
凝集シリカ粉末、倚孔質シリカ粉末を粉砕したシリカ粉
末、アルミナ等が挙げられ、特に溶融シリカ粉末、球状
シリカ粉末及び溶融シリカ粉末ず球状シリカ粉末ずの混
合物が奜たしい。たた無機質充填材の配合量ずしおは、
耐半田ストレス性ず成圢性のバランスから、総暹脂組成
物䞭に〜重量含たれるものが望たしい。
Examples of the inorganic filler used in the present invention include fused silica powder, spherical silica powder, crystalline silica powder, secondary agglomerated silica powder, silica powder obtained by crushing porous silica powder, alumina, etc., and particularly fused silica. Powders, spherical silica powders and mixtures of fused silica powders and spherical silica powders are preferred. In addition, as the compounding amount of the inorganic filler,
From the standpoint of balance between solder stress resistance and moldability, it is desirable that the total resin composition contains 70 to 90% by weight.

【】さらに本発明に甚いる硬化促進剀ぱポキ
シ基ず氎酞基の反応を促進するものであれば良く、䞀般
に封止材料に䜿甚されおいるものを広く䜿甚するこずが
できる。䟋えばトリフェニルホスフィン、ト
リブチルホスフィン、トリ−メチルフェニルホス
フィン等の有機ホスフィン化合物、トリブチルアミン、
トリ゚チルアミン、ベンゞルゞメチルアミン、トリスゞ
メチルアミノメチルフェノヌル、−ゞアザビシク
ロ−−りンデセン等の第
玚アミン、−メチルむミダゟヌル、−フェニルむミ
ダゟヌル、−゚チル−−メチルむミダゟヌル等のむ
ミダゟヌル化合物等が挙げられる。これらを単独で甚い
おも、あるいはその皮以䞊を䜵甚するこずも可胜であ
る。
Further, the curing accelerator used in the present invention may be any one as long as it accelerates the reaction between the epoxy group and the hydroxyl group, and those generally used for the sealing material can be widely used. For example, organic phosphine compounds such as triphenylphosphine (TPP), tributylphosphine, tri (4-methylphenyl) phosphine, tributylamine,
Third such as triethylamine, benzyldimethylamine, trisdimethylaminomethylphenol, 1,8-diazabicyclo [5,4,0] -7-undecene (DBU)
Examples thereof include imidazole compounds such as secondary amine, 2-methylimidazole, 2-phenylimidazole and 2-ethyl-4-methylimidazole. These may be used alone or in combination of two or more.

【】本発明の組成物は前述のもの以倖、必芁に
応じおカヌボンブラック等の着色剀、カルナバワック
ス、合成ワックス等の離型剀、ブロム化゚ポキシ、䞉酞
化アンチモン等の難燃剀、γ−グリシドキシプロピルト
リメトキシシラン等のカップリング剀、シリコヌンゎ
ム、ポリブタゞ゚ン等のゎム成分を添加するこずができ
る。
In addition to the above, the composition of the present invention may optionally contain a coloring agent such as carbon black, a release agent such as carnauba wax and synthetic wax, a flame retardant such as brominated epoxy and antimony trioxide, and γ-. A coupling agent such as glycidoxypropyltrimethoxysilane and a rubber component such as silicone rubber and polybutadiene can be added.

【】又、本発明の封止甚゚ポキシ暹脂組成物を
成圢材料ずしお補造するには、゚ポキシ暹脂、硬化剀、
硬化促進剀、充填剀、その他の添加剀をミキサヌ等によ
っお十分に均䞀に混合した埌、さらに熱ロヌルたたはニ
ヌダヌ等で溶融混緎し、冷华埌粉砕しお成圢材料ずする
こずができる。これらの成圢材料は電子郚品あるいは電
気郚品の封止、被芆、絶瞁等に適甚するこずができる。
To produce the encapsulating epoxy resin composition of the present invention as a molding material, an epoxy resin, a curing agent,
A curing accelerator, a filler, and other additives are sufficiently and uniformly mixed with a mixer or the like, and then melt-kneaded with a hot roll, a kneader, or the like, cooled, and then pulverized to obtain a molding material. These molding materials can be applied to sealing, coating, insulating, etc. of electronic parts or electric parts.

【】[0020]

【実斜䟋】以䞋本発明を実斜䟋で具䜓的に説明する。EXAMPLES The present invention will be specifically described below with reference to examples.

【】実斜䟋 䞋蚘組成物 オル゜クレゟヌルずβ−ナフトヌルの共瞮合ノボラック゚ポキシ暹脂 はが重量、が重量の混合物、 ゚ポキシ圓量、軟化点℃ 3.重量郚 䞋蚘匏で瀺されるフェノヌル暹脂硬化剀 はが重量、が重量の混合物、 氎酞基圓量軟化点℃ 0.重量 郚Example 1 The following composition Co-condensed novolak epoxy resin of orthocresol and β-naphthol (n is a mixture of 70% by weight of n = 3 and 30% by weight of n = 4, epoxy equivalent 225, softening point 84 ° C.) ) 13.5 parts by weight Phenolic resin curing agent represented by the following formula (3) (n is a mixture in which n = 2 is 30% by weight and n = 3 is 70% by weight, hydroxyl equivalent 175, softening point 75 ° C.) 10. 5 parts by weight

【】[0022]

【化】 [Chemical 5]

【】 溶融シリカ粉末 重量郚 トリフェニルホスフィン 0.重量郚 カヌボンブラック 0.重量郚 カルナバワックス 0.重量郚 をミキサヌで垞枩で混合し、〜℃で軞ロヌ
ルにより混緎し、冷华埌粉砕した成圢材料ずした埗られ
た成圢材料をタブレット化し、䜎圧トランスファヌ成圢
機にお℃、kgcm2 、秒の条件で半田
クラック詊隓甚ずしお×mmのチップをパッケ
ヌゞに封入し、たた半田耐湿詊隓甚ずしお×mmのチ
ップをパッケヌゞに封入した。封止したテ
スト甚玠子に぀いお䞋蚘の半田クラック詊隓及び半田耐
湿性詊隓を行った。
75 parts by weight of fused silica powder 0.2 parts by weight of triphenylphosphine 0.3 parts by weight of carbon black 0.5 parts by weight of carnauba wax are mixed in a mixer at room temperature and kneaded by a twin-screw roll at 70 to 100 ° C. The obtained molding material was made into a molding material that was crushed after cooling, and the obtained molding material was tabletized and a 6 × 6 mm chip was put in a 52p package for solder crack testing under the conditions of 175 ° C., 70 kg / cm 2 and 120 seconds on a low-pressure transfer molding machine. And a 3 × 6 mm chip for a solder moisture resistance test in a 16 pSOP package. The sealed test element was subjected to the following solder crack test and solder moisture resistance test.

【】半田クラック詊隓封止したテスト甚玠子
を℃、の環境䞋で及び
凊理し、その埌℃の半田槜に秒間浞挬埌、顕
埮鏡で倖郚クラックを芳察した。 半田耐湿性詊隓封止したテスト甚玠子を℃、
の環境䞋で凊理しその埌℃の半田
槜に秒間浞挬埌、プレッシャヌクッカヌ詊隓
℃、を行い、回路のオヌプン䞍良を枬
定した。 詊隓結果を衚に瀺す。
Solder crack test: The sealed test element was subjected to an environment of 85 ° C. and 85% RH for 48 hours and 72 hours.
After processing, it was immersed in a solder bath at 260 ° C. for 10 seconds, and external cracks were observed with a microscope. Solder moisture resistance test: sealed test element at 85 ° C, 85
After 72 Hr treatment in an environment of% RH and then dipping in a solder bath at 260 ° C for 10 seconds, a pressure cooker test (12
The circuit was opened at 5 ° C. and 100% RH, and the open circuit failure was measured. The test results are shown in Table 1.

【】実斜䟋〜 衚の凊方にしたがっお配合し、実斜䟋ず同様にしお
成圢材料を埗た。この成圢材料でテスト甚玠子を封止し
た成圢品を埗、この成圢品を甚いお実斜䟋ず同様に半
田クラック詊隓及び半田耐湿性詊隓を行った。詊隓結果
を衚に瀺す。
Examples 2 to 5 Compounding was performed according to the formulation shown in Table 1, and molding materials were obtained in the same manner as in Example 1. A molded product in which a test element was sealed with this molding material was obtained, and a solder crack test and a solder moisture resistance test were conducted using this molded product in the same manner as in Example 1. The test results are shown in Table 1.

【】比范䟋〜 衚の凊方にしたがっお配合し、実斜䟋ず同様にしお
成圢材料を埗た。この成圢材料でテスト甚玠子を封止し
た成圢品を埗、この成圢品を甚いお実斜䟋ず同様に半
田クラック詊隓及び半田耐湿性詊隓を行った。詊隓結果
を衚に瀺す。
Comparative Examples 1 to 5 Compounding was carried out according to the formulation shown in Table 1, and a molding material was obtained in the same manner as in Example 1. A molded product in which a test element was sealed with this molding material was obtained, and a solder crack test and a solder moisture resistance test were conducted using this molded product in the same manner as in Example 1. The test results are shown in Table 1.

【】[0027]

【衚】 [Table 1]

【】[0028]

【発明の効果】耐熱性、䜎吞氎性、可撓性に優れた暹脂
組成物が埗られる。プリント回路基板に衚面実装する高
集積パッケヌゞ甚封止材料ずしお半田付け時の半田
耐熱性に非垞に優れおいる。
EFFECT OF THE INVENTION A resin composition having excellent heat resistance, low water absorption and flexibility can be obtained. As a sealing material for highly integrated IC packages to be surface-mounted on a printed circuit board, it has excellent solder heat resistance during soldering.

───────────────────────────────────────────────────── フロントペヌゞの続き (51)Int.Cl.5 識別蚘号 庁内敎理番号  技術衚瀺箇所  63/00  8830−4 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Internal reference number FI technical display location C08L 63/00 MJS 8830-4J

Claims (1)

【特蚱請求の範囲】[Claims] 【請求項】 䞋蚘匏で瀺されるオル゜ク
レゟヌルずβ−ナフトヌルの共瞮合ノボラック゚ポキシ
暹脂を総゚ポキシ暹脂量の〜重量含む゚ポ
キシ暹脂、 【化】 〜 䞋蚘匏で瀺されるフェノヌル暹脂硬化剀を
総硬化剀量に察しお〜重量含む硬化剀、 【化】 匏䞭の1 、2 は氎玠、ハロゲン、䜎玚アルキル基
の䞭から遞択される同䞀もしくは異なる原子たたは基、
〜 無機質充填材及び 硬化促進剀 を必須成分ずする半導䜓封止甚゚ポキシ暹脂組成物。
1. An epoxy resin containing (A) an orthocresol and β-naphthol co-condensed novolac epoxy resin represented by the following formula (1) in an amount of 30 to 100% by weight of the total epoxy resin: (N = 1 to 6) (B) A curing agent containing a phenol resin curing agent represented by the following formula (2) in an amount of 30 to 100% by weight based on the total amount of the curing agent: (Wherein R 1 and R 2 are the same or different atoms or groups selected from hydrogen, halogen and lower alkyl groups,
n = 1 to 6) An epoxy resin composition for semiconductor encapsulation, which comprises (C) an inorganic filler and (D) a curing accelerator as essential components.
JP32927791A 1991-12-13 1991-12-13 Epoxy resin composition Expired - Fee Related JP2963260B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP32927791A JP2963260B2 (en) 1991-12-13 1991-12-13 Epoxy resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP32927791A JP2963260B2 (en) 1991-12-13 1991-12-13 Epoxy resin composition

Publications (2)

Publication Number Publication Date
JPH05166974A true JPH05166974A (en) 1993-07-02
JP2963260B2 JP2963260B2 (en) 1999-10-18

Family

ID=18219656

Family Applications (1)

Application Number Title Priority Date Filing Date
JP32927791A Expired - Fee Related JP2963260B2 (en) 1991-12-13 1991-12-13 Epoxy resin composition

Country Status (1)

Country Link
JP (1) JP2963260B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010013406A1 (en) * 2008-08-01 2010-02-04 䜏友ベヌクラむト株匏䌚瀟 Resin composition for semiconductor encapsulation and semiconductor device using the same
JP2013010903A (en) * 2011-06-30 2013-01-17 Dic Corp Epoxy resin, curing resin composition, cured product thereof, semiconductor sealing material, and printed wiring board
US8424652B2 (en) 2007-03-23 2013-04-23 Otis Elevator Company Electromagnet and elevator door coupler
TWI624487B (en) * 2014-02-21 2018-05-21 Nipponkayaku Kk Epoxy resin, epoxy resin composition and cured product thereof

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8424652B2 (en) 2007-03-23 2013-04-23 Otis Elevator Company Electromagnet and elevator door coupler
WO2010013406A1 (en) * 2008-08-01 2010-02-04 䜏友ベヌクラむト株匏䌚瀟 Resin composition for semiconductor encapsulation and semiconductor device using the same
JPWO2010013406A1 (en) * 2008-08-01 2012-01-05 䜏友ベヌクラむト株匏䌚瀟 Semiconductor sealing resin composition and semiconductor device using the same
US8552572B2 (en) 2008-08-01 2013-10-08 Sumitomo Bakelite Co., Ltd. Resin composition for encapsulating semiconductor and semiconductor device using the same
JP2013010903A (en) * 2011-06-30 2013-01-17 Dic Corp Epoxy resin, curing resin composition, cured product thereof, semiconductor sealing material, and printed wiring board
TWI624487B (en) * 2014-02-21 2018-05-21 Nipponkayaku Kk Epoxy resin, epoxy resin composition and cured product thereof

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