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JPH10287793A - Epoxy resin composition for semiconductor sealing and semiconductor device sealed therewith - Google Patents

Epoxy resin composition for semiconductor sealing and semiconductor device sealed therewith

Info

Publication number
JPH10287793A
JPH10287793A JP9855197A JP9855197A JPH10287793A JP H10287793 A JPH10287793 A JP H10287793A JP 9855197 A JP9855197 A JP 9855197A JP 9855197 A JP9855197 A JP 9855197A JP H10287793 A JPH10287793 A JP H10287793A
Authority
JP
Japan
Prior art keywords
epoxy resin
resin composition
formula
represented
weight
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
JP9855197A
Other languages
Japanese (ja)
Inventor
Tatsuo Kawada
達男 河田
Akira Omori
明 大森
Junichi Seki
淳一 関
Terumi Tsukahara
輝巳 塚原
Masanobu Fujii
昌信 藤井
Hirooki Koujima
博起 幸島
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.)
Resonac Corp
Original Assignee
Hitachi Chemical 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 Hitachi Chemical Co Ltd filed Critical Hitachi Chemical Co Ltd
Priority to JP9855197A priority Critical patent/JPH10287793A/en
Publication of JPH10287793A publication Critical patent/JPH10287793A/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

PROBLEM TO BE SOLVED: To obtain a composition excellent in humidity resistance and soldering reflow resistance by mixing an epoxy resin containing a specified or larger amount of an epoxy resin having a dicyclopentadiene skeleton with a compound having a plurality of phenolic hydroxyl groups, a phosphorus compound and an inorganic filler in a specified ratio. SOLUTION: The epoxy resin used contains at least 70 wt.% epoxy resin represented by formula I. The phosphorus compound used is one represented by formula II. The inorganic filler is used in an amount of 60-95 wt.% based on the total weight of the composition. The epoxy resin used may entirely consists of an epoxy resin represented by formula I or a combination thereof with another epoxy resin having at least two epoxy groups. The resin used in combination is one represented by formula III (wherein R is H or a 1-4C alkyl; and m is 0-6). The compound having a phenolic hydroxyl group is desirably a compound represented by formula IV (wherein p is 0-6). The inorganic filler used is exemplified by a fused silica powder.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、半導体素子の表面
実装化における耐湿性及び耐半田リフロー性に優れた半
導体封止用エポキシ樹脂組成物及びそれを用いた樹脂封
止型半導体装置に関する。
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 moisture resistance and solder reflow resistance in surface mounting of a semiconductor element, and a resin-encapsulated semiconductor device using the same.

【0002】[0002]

【従来の技術】従来、ダイオード、トランジスター、I
C、LSI等の半導体装置を熱硬化性樹脂で封止してい
るが、特に、IC、LSI等の半導体装置では耐熱性、
耐湿性に優れたオルソクレゾールノボラック型エポキシ
樹脂をフェノールノボラック樹脂で硬化させ、充填材と
して溶融シリカ、結晶シリカ等の無機充填材を配合した
エポキシ樹脂組成物が用いられている。ところが、近年
IC、LSI等の半導体装置の高集積化に伴いチップが
段々大型化し、かつパッケージは、従来のDIPタイプ
から表面実装化された小型、薄型のQFP、SOP、T
SOP、SOJ、TQFP、PLCCに変わってきてい
る。すなわち、大型チップを小型で薄いパッケージに封
入することになり、熱応力によりクラックが発生し、こ
れらのクラックによる耐湿性の低下等の問題が大きくク
ローズアップされている。特に、はんダ付の行程におい
て、IRリフローやVPSリフロー等の装置を用いるた
め、急激に200℃以上の高温にさらされることによ
り、パッケージ中に含有される水分が気化し、この蒸気
圧が樹脂と素子/リードフレーム等のインサートとの界
面において剥離応力として働き、これら界面での剥離、
薄型のパッケージでは、フクレや割れが発生し耐湿性が
劣化してしまうという問題点がでてきている。このよう
な問題点を解決しようといろいろな検討がなされてお
り、これまでに各種の樹脂による検討では、インサート
に対する接着力、硬化物の吸湿性、高温での強度が重要
であることが分かっている。一方、インサートに対して
強い接着力を示す場合、成形金型との離型性が悪いとい
った問題が生じていた。また、充填材料を多くすること
は低吸湿化、高強度化に対して有効ではあるが、流動性
を低下させるといった問題があり、これは、樹脂の粘度
にも影響される。このため、樹脂の硬化物では吸水率を
小さくできる系でも、その系の粘度が高く充填材料を多
く添加できないといった問題点が生じている。また、樹
脂系によっては、エポキシ樹脂組成物の保存安定性が著
しく悪いと言った問題を生じている。従って、これらの
大型チップを封止するのに適した信頼性の高い半導体封
止用樹脂組成物の開発が望まれている。
2. Description of the Related Art Conventionally, diodes, transistors, I
Although semiconductor devices such as C and LSI are sealed with a thermosetting resin, heat resistance is particularly high in semiconductor devices such as IC and LSI.
An epoxy resin composition obtained by curing an orthocresol novolak type epoxy resin having excellent moisture resistance with a phenol novolak resin and blending an inorganic filler such as fused silica or crystalline silica as a filler is used. However, in recent years, as the integration of semiconductor devices such as ICs and LSIs has increased, the size of chips has gradually increased, and packages have become smaller and thinner QFPs, SOPs, TPSs, which are surface-mounted from conventional DIP types.
SOP, SOJ, TQFP, PLCC have been changed. That is, a large chip is sealed in a small and thin package, and cracks are generated by thermal stress, and problems such as a decrease in moisture resistance due to these cracks are greatly highlighted. In particular, in the process with soldering, since equipment such as IR reflow and VPS reflow is used, the moisture contained in the package is vaporized by being rapidly exposed to a high temperature of 200 ° C. or more, and this vapor pressure is reduced. It acts as peeling stress at the interface between the resin and the insert such as the element / lead frame, and peeling at these interfaces.
In the case of a thin package, there is a problem that blisters and cracks are generated and the moisture resistance is deteriorated. Various studies have been made to solve such problems.Investigations using various resins have revealed that the adhesive strength to the insert, the moisture absorption of the cured product, and the strength at high temperatures are important. I have. On the other hand, when a strong adhesive force is exhibited to the insert, there has been a problem that the releasability from a molding die is poor. Although increasing the amount of the filling material is effective for lowering the moisture absorption and increasing the strength, there is a problem in that the fluidity is reduced, which is also affected by the viscosity of the resin. For this reason, even in a system that can reduce the water absorption of a cured product of a resin, there is a problem that the viscosity of the system is high and a large amount of filler cannot be added. Further, some resin systems have a problem that the storage stability of the epoxy resin composition is extremely poor. Therefore, development of a highly reliable semiconductor sealing resin composition suitable for sealing these large chips is desired.

【0003】[0003]

【発明が解決しようとする課題】本発明は、このような
問題に対して、半導体封止用に用いるエポキシ樹脂組成
物において、インサートとの密着性と成形金型との離型
性を両立し、充填材が多いにもかかわらず優れた流動性
をもった半導体パッケージの基板への実装時におけるパ
ッケージの耐はんだストレス性を著しく向上させた半導
体封止用エポキシ樹脂組成物を提供するところにある。
SUMMARY OF THE INVENTION In order to solve the above-mentioned problems, an object of the present invention is to provide an epoxy resin composition used for semiconductor encapsulation which achieves both adhesion to an insert and release from a molding die. An object of the present invention is to provide an epoxy resin composition for semiconductor encapsulation which has significantly improved soldering stress resistance of a package when mounted on a substrate of a semiconductor package having excellent fluidity despite a large amount of filler. .

【0004】[0004]

【課題を解決するための手段】本発明者らは、上記課題
を解決するために鋭意研究を重ねた結果、エポキシ樹脂
と硬化剤として特定の樹脂と特定の化合物とを組み合わ
せて含有させたエポキシ樹脂組成物が低吸湿、高接着の
点で優れ、同時に基板へのはんだ付け実装時のクラック
に対して有効であることを見出した。また、そのエポキ
シ樹脂組成物に特定のリン化合物を硬化促進剤として含
有させると、流動性に富み充填材の高充填化が可能であ
り、かつ保存性に富んでいるエポキシ樹脂組成物が得ら
れることを見出し、この知見に基づいて本発明を完成す
るに至った。すなわち、本発明は、下記(A)〜(D)
成分からなる半導体封止用エポキシ樹脂組成物及びそれ
を用いた樹脂封止型半導体装置に関する。 (A)下記構造式1で表されるエポキシ樹脂、
Means for Solving the Problems The present inventors have conducted intensive studies in order to solve the above-mentioned problems, and as a result, have found that an epoxy resin containing a specific resin and a specific compound as a curing agent in combination is contained. It has been found that the resin composition is excellent in low moisture absorption and high adhesion, and at the same time is effective against cracks during solder mounting on a substrate. Further, when the epoxy resin composition contains a specific phosphorus compound as a curing accelerator, it is possible to obtain an epoxy resin composition which is rich in fluidity, can be highly filled with a filler, and has excellent storage stability. This led to the completion of the present invention based on this finding. That is, the present invention provides the following (A) to (D)
The present invention relates to an epoxy resin composition for semiconductor encapsulation comprising components and a resin-encapsulated semiconductor device using the same. (A) an epoxy resin represented by the following structural formula 1,

【化5】 (B)1分子中に2個以上のフェノール性水酸基を有す
る化合物、(C)下記構造式2で表されるリン化合物
Embedded image (B) a compound having two or more phenolic hydroxyl groups in one molecule, (C) a phosphorus compound represented by the following structural formula 2

【化6】 及び(D)エポキシ樹脂組成物総量中60〜95重量%
の無機充填材。
Embedded image And (D) 60 to 95% by weight based on the total amount of the epoxy resin composition
Inorganic filler.

【0005】[0005]

【発明の実施の形態】(A)成分のエポキシ樹脂は上記
構造式1で表されるエポキシ樹脂のみからなるものであ
ってもよいし、それ以外に1分子中に2個以上のエポキ
シ基を有する他のエポキシ樹脂を、総エポキシ樹脂中の
30重量%まで併用してもよい。併用されるエポキシ樹
脂としては、オルソクレゾールノボラック型エポキシ樹
脂、フェノールノボラック型エポキシ樹脂、ビスフェノ
ールA型エポキシ樹脂等が挙げられるが、好適には下記
構造式3で表されるエポキシ樹脂を全エポキシ樹脂に対
し、2〜30重量%、好ましくは10〜20重量%の割
合で用いると、より流動性を向上することが出来、充填
材の高充填化の点からも好ましい。この場合、2重量%
未満では流動性向上の効果が乏しく、また30重量%を
越えて配合すると離型性が悪化することがある。
BEST MODE FOR CARRYING OUT THE INVENTION The epoxy resin of the component (A) may consist solely of the epoxy resin represented by the above structural formula 1, or may contain two or more epoxy groups in one molecule. Other epoxy resins may be used in combination up to 30% by weight of the total epoxy resin. Examples of the epoxy resin used in combination include orthocresol novolak type epoxy resin, phenol novolak type epoxy resin, bisphenol A type epoxy resin, and the like. Preferably, the epoxy resin represented by the following structural formula 3 is used as the total epoxy resin. On the other hand, when it is used at a ratio of 2 to 30% by weight, preferably 10 to 20% by weight, the fluidity can be further improved, which is preferable from the viewpoint of increasing the filling of the filler. In this case, 2% by weight
If the amount is less than 30%, the effect of improving the fluidity is poor. If the amount exceeds 30% by weight, the releasability may be deteriorated.

【化7】 (式中、Rは水素原子または炭素数1〜4の低級アルキ
ル基を表し、mは0〜6の整数を表す。) なお、構造式3で表されるエポキシ樹脂は、1種単独で
用いても良いし、2種以上を併用しても良い。
Embedded image (In the formula, R represents a hydrogen atom or a lower alkyl group having 1 to 4 carbon atoms, and m represents an integer of 0 to 6.) The epoxy resin represented by Structural Formula 3 is used singly. Or two or more of them may be used in combination.

【0006】硬化剤として用いられる(B)成分の1分
子中に2個以上のフェノール性水酸基を有する化合物と
しては、フェノールノボラック樹脂、クレゾールノボラ
ック樹脂等が挙げられるが、好適には下記構造式4で示
される化合物を用いることが高接着力化、低吸湿率化の
点より好ましい。また、これらを2種以上併用しても良
い。
Examples of the compound having two or more phenolic hydroxyl groups in one molecule of the component (B) used as a curing agent include a phenol novolak resin and a cresol novolak resin. It is preferable to use a compound represented by the following formulas from the viewpoint of increasing the adhesive strength and reducing the moisture absorption. Further, two or more of these may be used in combination.

【化8】 (式中、pは0〜6の整数を表す。)Embedded image (In the formula, p represents an integer of 0 to 6.)

【0007】(C)成分の構造式2で示されるリン化合
物は硬化促進剤として用いられ、このリン化合物を用い
ることにより流動性に富み、充填材の高充填化の点で優
れたエポキシ樹脂組成物が得られる。また、このリン化
合物を含有する本発明のエポキシ樹脂組成物は保存安定
性の点でも優れている。構造式2で表されるリン化合物
は、たとえば、以下の方法によって得られる。 1.トリフェルニホスフィン41.6gをアセトン12
0gに溶解する。 2.p−ベンゾキノン17.6gをアセトン120gに
溶解する。 3.1と2の溶液を室温〜80℃で混合する。 4.析出した黄褐色結晶を濾過して取り出し、構造式2
で示されるリン化合物として用いる。ここで、溶剤とし
て上記アセトンの代わりにアセトンとトルエンの混合溶
剤等を用いても良い。 (C)成分の配合割合は総エポキシ樹脂100重量部に
対して通常0.1〜10重量部、好ましくは2〜7重量
部が適当である。また、硬化促進剤として、構造式2で
表されるリン化合物以外の他の硬化促進剤、例えば、ト
リフェニルホスフィン、1,8−ジアザビシクロ(2.
4.6)ウンデセン−7等を併用してもよい。
[0007] The phosphorus compound represented by the structural formula 2 of the component (C) is used as a curing accelerator. By using this phosphorus compound, an epoxy resin composition which is rich in fluidity and excellent in high filling of the filler. Things are obtained. Further, the epoxy resin composition of the present invention containing the phosphorus compound is also excellent in storage stability. The phosphorus compound represented by the structural formula 2 is obtained, for example, by the following method. 1. 41.6 g of triferniphosphine in acetone 12
Dissolve in 0 g. 2. 17.6 g of p-benzoquinone are dissolved in 120 g of acetone. 3. Mix the solutions of 1 and 2 at room temperature to 80 ° C. 4. The precipitated yellow-brown crystals were filtered out and taken out according to Structural Formula 2
Used as a phosphorus compound represented by Here, a mixed solvent of acetone and toluene or the like may be used as the solvent instead of the acetone. The proportion of the component (C) is usually 0.1 to 10 parts by weight, preferably 2 to 7 parts by weight, per 100 parts by weight of the total epoxy resin. Further, as a curing accelerator, a curing accelerator other than the phosphorus compound represented by the structural formula 2, for example, triphenylphosphine, 1,8-diazabicyclo (2.
4.6) Undecene-7 or the like may be used in combination.

【0008】また、本発明のエポキシ樹脂組成物には、
成型時に金型との良好な離型性を持たせるため離型剤を
添加しても良い。この離型剤としては、酸化型若しくは
非酸化型のポリオレフィンを総エポキシ樹脂100重量
部に対して0.01〜10重量部、好ましくは0.1〜
5重量部添加することが好ましい。これは、0.01重
量部未満では十分な離型性を得ることができず、また、
10重量部を越えると接着性が阻害される恐れがあるか
らである。この酸化型若しくは非酸化型のオレフィンと
してはヘキスト社製のH4やPE、PEDシリーズ等の
平均分子量が500〜10000程度の低分子量ポリエ
チレン等が挙げられる。また、これ以外の離型剤、例え
ば、カルナバワックス、モンタン酸エステル、モンタン
酸、ステアリン酸等と併用しても良い。酸化型若しくは
非酸化型のポリオレフィンに加えてこれら他の離型剤を
併用する場合、その配合割合は総エポキシ樹脂100重
量部に対して通常0.1〜10重量部、好ましくは0.
5〜3重量部の範囲が適当である。
Further, the epoxy resin composition of the present invention comprises:
A releasing agent may be added in order to have good releasability from the mold during molding. As the release agent, an oxidized or non-oxidized polyolefin is used in an amount of 0.01 to 10 parts by weight, preferably 0.1 to 10 parts by weight, based on 100 parts by weight of the total epoxy resin.
It is preferable to add 5 parts by weight. This means that if it is less than 0.01 part by weight, sufficient release properties cannot be obtained, and
If it exceeds 10 parts by weight, the adhesiveness may be impaired. Examples of the oxidized or non-oxidized olefin include low molecular weight polyethylene having an average molecular weight of about 500 to 10,000 such as H4, PE, and PED series manufactured by Hoechst. Further, it may be used in combination with other release agents such as carnauba wax, montanic acid ester, montanic acid, and stearic acid. When these other release agents are used in addition to the oxidized or non-oxidized polyolefin, the mixing ratio thereof is usually 0.1 to 10 parts by weight, preferably 0.1 to 10 parts by weight, per 100 parts by weight of the total epoxy resin.
A range of 5 to 3 parts by weight is suitable.

【0009】ところで、構造式1で示されるエポキシ樹
脂を用いた場合、エポキシ樹脂組成物の難燃性が低下す
る。このため難燃剤を従来のオルソクレゾール型エポキ
シ樹脂を用いたエポキシ樹脂組成物において、使用する
よりも多量に配合することが好ましい。本発明において
好適に用いられる難燃剤としては、例えば、ブロム化エ
ポキシ樹脂等の有機難燃剤や三酸化アンチモン等の無機
難燃剤が挙げられる。また、これらの難燃剤をより多く
配合した場合、イオン性の不純物が多くなり、半導体装
置の信頼性を損なうことがある。このため、この様なエ
ポキシ樹脂組成物には、下記式5で示される無機イオン
捕捉剤(合成ハイドロタルサイト)を配合することが好
ましい。この無機イオン捕捉剤の配合割合は、総エポキ
シ樹脂100重量部に対して、通常0.1〜30重量
部、好ましくは1〜5重量部の範囲が適当である。 Mg4.5 Al2 (OH)13CO3 ・3.5H2 O 式5 (D)成分の無機充填材としては、例えば、溶融シリカ
粉末、結晶シリカ粉末、アルミナ、窒化アルミ、窒化ケ
イ素等が用いられる。その形状としては、球状、不定
形、楕円状のもの等が用いられる。また、その配合割合
はエポキシ樹脂組成物総量中60〜95重量%配合され
る。60重量%未満では十分な耐リフロークラック性を
維持することが出来ず、また、95重量%を越えると成
形ために十分な流動性を維持することが出来ないためで
ある。また、本発明に用いられるエポキシ樹脂組成物に
は必要に応じてカーボンブラック等の顔料、シランカッ
プリング剤等のカップリング剤、シリコーン等の添加剤
類を配合することができる。
By the way, when the epoxy resin represented by the structural formula 1 is used, the flame retardancy of the epoxy resin composition decreases. For this reason, it is preferable to add a flame retardant in an epoxy resin composition using a conventional orthocresol type epoxy resin in a larger amount than that used. Examples of the flame retardant suitably used in the present invention include an organic flame retardant such as a brominated epoxy resin and an inorganic flame retardant such as antimony trioxide. Further, when more of these flame retardants are blended, ionic impurities increase, and the reliability of the semiconductor device may be impaired. For this reason, it is preferable to blend an inorganic ion scavenger (synthetic hydrotalcite) represented by the following formula 5 into such an epoxy resin composition. The mixing ratio of the inorganic ion scavenger is usually from 0.1 to 30 parts by weight, preferably from 1 to 5 parts by weight, based on 100 parts by weight of the total epoxy resin. Mg 4.5 Al 2 (OH) 13 CO 3 .3.5H 2 O As the inorganic filler of the formula 5 (D) component, for example, fused silica powder, crystalline silica powder, alumina, aluminum nitride, silicon nitride and the like are used. . As the shape, a spherical shape, an irregular shape, an elliptical shape, or the like is used. The mixing ratio is 60 to 95% by weight based on the total amount of the epoxy resin composition. If it is less than 60% by weight, sufficient reflow crack resistance cannot be maintained, and if it exceeds 95% by weight, sufficient fluidity for molding cannot be maintained. Further, the epoxy resin composition used in the present invention may optionally contain a pigment such as carbon black, a coupling agent such as a silane coupling agent, and additives such as silicone.

【0010】上記原材料を各々適宣配合し、この配合物
をミキシングロール機等の混練機にかけ混練して半溶融
状態の樹脂組成物とし、これを室温に冷却した後、公知
の手段により粉砕し、必要に応じて打錠するといって一
連の工程により、目的とする半導体封止用エポキシ樹脂
組成物を得ることができる。本発明の半導体封止用エポ
キシ樹脂組成物は、通常粉末状またはそれを打錠したタ
ブレット錠の材料として、半導体の封止に用いられる。
本発明のエポキシ樹脂組成物を用いて、半導体素子を封
止すると目的とする半導体装置が得られる。半導体素子
の封止方法は特に限定するものではなく、通常の方法、
例えば、トランスファー成形等の公知の成形方法によっ
て行うことができる。このようにして得られる半導体装
置は、インサートと封止材料の接着性に優れ、封止材料
への吸湿量が少なく、装置を基板にはんだ付けする際の
耐クラック性に優れていると同時に、半導体装置をトラ
ンスファー成形する際に金型側へ張り付くこともなく優
れた封止作業性を有している。
The above-mentioned raw materials are appropriately blended, and the blends are kneaded in a kneading machine such as a mixing roll machine to form a semi-molten resin composition, which is cooled to room temperature and pulverized by a known means. The desired epoxy resin composition for encapsulating a semiconductor can be obtained through a series of steps of tableting as required. The epoxy resin composition for semiconductor encapsulation of the present invention is usually used for encapsulating semiconductors as a powder or as a material for tablet tablets obtained by compressing it.
When a semiconductor element is sealed using the epoxy resin composition of the present invention, a target semiconductor device is obtained. The method for encapsulating the semiconductor element is not particularly limited, and a normal method,
For example, it can be performed by a known molding method such as transfer molding. The semiconductor device obtained in this way has excellent adhesiveness between the insert and the sealing material, has a small amount of moisture absorption into the sealing material, and has excellent crack resistance when soldering the device to a substrate, It has excellent sealing workability without sticking to the mold side when transfer molding a semiconductor device.

【0011】[0011]

【実施例】以下、本発明の実施例及び比較例によって本
発明を更に具体的に説明するが、本発明はこれらの実施
例に限定されるものではない。まず、表1及び表2に示
す重量部で各材料を配合し予備混合した後、10インチ
径の2軸ロールを使用して、混練温度80〜90℃、混
練時間7〜12分の条件でし混練し、冷却後粉砕して半
導体封止用エポキシ樹脂組成物を得た。この封止用エポ
キシ樹脂組成物を用い、トランスファー成型機で、金型
温度180℃、成形圧力70kgf/cm2 、硬化時間90秒
の条件で成形し、試験片を作成した。後硬化は175
℃、6時間行った。スパイラルフローは、EMMI1−
66に準じて測定した。熱時硬度は、上記条件で成形し
た成型品のショア硬度を測定した。Alピール接着力
は、厚み約0.03mmのアルミホイル上に成形した幅1
0mmの成形品にて測定した。吸水率は上記成形条件にて
φ50×3mmt の円板を成形し、PCT20h後の吸水
率を求めた。耐リフロークラック性は、QFP14×2
0×2.0mmt のパッケージを用い上記条件にて成形
後、85℃/85RH%の雰囲気にX時間放置した後、
IRリフロー炉にて加熱(炉内温度:MAX245℃)
し、クラックの有無を超音波顕微鏡にて観察した。表1
及び表2中のB/Aについて、Aは試験に供したパッケ
ージ数を、Bはクラックの発生が観察されたパッケージ
の数を示す。離型性はCrメッキを行ったステンレス板
表面に、20mmφの成型品を連続成形し、金属板と封止
材の剪断接着力の変化から判定した。◎は5shot以内で
0kgf となったものを、○は5〜10shotで0kgf とな
ったものを、×は10shot成形しても0kgf とならなか
ったものを表す。表2中、高温放置(175℃)とは、
パッケージを175℃おいて放置してデバイスが不良品
となった時間を表す。表1に実施例1〜4及び比較例1
〜4の結果を示す。表2に実施例5,6及び比較例5,
6の結果を示す。これらの結果から判るように、本発明
の半導体封止用エポキシ樹脂組成物は耐リフロークラッ
ク性、高温放置性、離型性等に優れている。
EXAMPLES Hereinafter, the present invention will be described more specifically with reference to examples and comparative examples of the present invention, but the present invention is not limited to these examples. First, after mixing and pre-mixing each material in parts by weight shown in Tables 1 and 2, using a biaxial roll having a diameter of 10 inches, at a kneading temperature of 80 to 90 ° C. and a kneading time of 7 to 12 minutes. Then, the mixture was cooled and pulverized to obtain an epoxy resin composition for semiconductor encapsulation. Using the epoxy resin composition for sealing, a transfer molding machine was used to mold at a mold temperature of 180 ° C., a molding pressure of 70 kgf / cm 2 , and a curing time of 90 seconds to prepare a test piece. Post cure 175
C. for 6 hours. Spiral flow is EMMI1-
66 was measured. The hardness at the time of heating measured the Shore hardness of the molded article molded under the above conditions. The adhesive strength of the Al peel is a width of 1 on an aluminum foil with a thickness of about 0.03 mm.
It was measured on a 0 mm molded product. The water absorption was determined by molding a disk of φ50 × 3 mmt under the above molding conditions and determining the water absorption after 20 hours of PCT. Reflow crack resistance is QFP14 × 2
After molding under the above conditions using a package of 0 × 2.0 mmt, and left in an atmosphere of 85 ° C./85 RH% for X hours,
Heating in IR reflow furnace (furnace temperature: MAX 245 ° C)
Then, the presence or absence of cracks was observed with an ultrasonic microscope. Table 1
And B / A in Table 2, A indicates the number of packages subjected to the test, and B indicates the number of packages in which cracks were observed. The releasability was determined by continuously forming a molded product of 20 mmφ on the surface of the Cr-plated stainless steel plate, and changing the shear adhesive force between the metal plate and the sealing material. ◎ indicates 0 kgf within 5 shots, ○ indicates 0 kgf within 5 to 10 shots, and x indicates 0 kgf after molding 10 shots. In Table 2, high temperature storage (175 ° C.)
This represents the time when the package was left at 175 ° C. and the device became defective. Table 1 shows Examples 1 to 4 and Comparative Example 1.
The results of No. to No. 4 are shown. Table 2 shows Examples 5 and 6 and Comparative Examples 5
6 shows the results. As can be seen from these results, the epoxy resin composition for semiconductor encapsulation of the present invention is excellent in reflow crack resistance, high-temperature storage properties, mold release properties, and the like.

【0012】[0012]

【表1】 その他の組成(実施例、比較例共通) シランカップリング剤 6部 カルナバワックス 2部 三酸化アンチモン 15部 カーボンブラック 2部 なお、構造式1のエポキシ樹脂としては、エポキシ当量
257の明和化成社製ZX−1257(商品名)を、構
造式3のエポキシ樹脂としては、エポキシ当量約192
の油化シェル社製YX−4000H(商品名)を、オル
ソクレゾールノボラック(OCN)としては、エポキシ
当量約200の住友化学社製ESCN−195(商品
名)をBr化エポキシ樹脂としては、エポキシ当量約3
75、臭素含有約50重量%の住友化学社製ESB−4
00T(商品名)を用いた。硬化剤のフェノールノボラ
ック樹脂としては、水酸基当量約106の日立化成社製
HP−850N(商品名)を用いた。
[Table 1] Other Compositions (Common to Examples and Comparative Examples) Silane coupling agent 6 parts Carnauba wax 2 parts Antimony trioxide 15 parts Carbon black 2 parts The epoxy resin of structural formula 1 is ZX manufactured by Meiwa Kasei Co., Ltd. having an epoxy equivalent of 257. -1257 (trade name) was used as the epoxy resin of structural formula 3 with an epoxy equivalent of about 192.
YX-4000H (trade name) manufactured by Yuka Shell Co., Ltd .; orthocresol novolak (OCN); ESCN-195 (trade name) manufactured by Sumitomo Chemical Co., Ltd. having an epoxy equivalent of about 200; About 3
75, ESB-4 manufactured by Sumitomo Chemical Co., Ltd. containing about 50% by weight of bromine
00T (trade name) was used. As a phenol novolak resin as a curing agent, HP-850N (trade name) manufactured by Hitachi Chemical Co., Ltd. having a hydroxyl equivalent of about 106 was used.

【0013】[0013]

【表2】 酸化15〜30mg KOH/g、数平均分子量約200
0の分岐型ポリエチレンワックス その他の組成(実施例、比較例共通) シランカップリング剤 6部 三酸化アンチモン 15部 カーボンブラック 2部
[Table 2] Oxidation 15-30 mg KOH / g, number average molecular weight about 200
Branched polyethylene wax of 0 Other composition (common to Examples and Comparative Examples) Silane coupling agent 6 parts Antimony trioxide 15 parts Carbon black 2 parts

【0014】[0014]

【発明の効果】本発明の半導体封止用エポキシ樹脂組成
物は、はんだ付け時の耐熱性及びその他の信頼性、成形
性に優れたものであり、従って該封止用樹脂組成物で封
止した半導体装置もはんだ付け時の耐熱性やその他の信
頼性に優れている。
The epoxy resin composition for semiconductor encapsulation of the present invention has excellent heat resistance during soldering, and other excellent reliability and moldability. Therefore, the epoxy resin composition for encapsulation with the encapsulation resin composition. The resulting semiconductor device also has excellent heat resistance and other reliability during soldering.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI C08K 3/22 C08K 3/22 3/26 3/26 5/524 5/524 H01L 23/29 H01L 23/30 R 23/31 //(C08L 63/00 23:00) (72)発明者 塚原 輝巳 茨城県結城市大字鹿窪1772−1 日立化成 工業株式会社下館工場内 (72)発明者 藤井 昌信 茨城県結城市大字鹿窪1772−1 日立化成 工業株式会社下館工場内 (72)発明者 幸島 博起 茨城県結城市大字鹿窪1772−1 日立化成 工業株式会社下館工場内──────────────────────────────────────────────────の Continued on the front page (51) Int.Cl. 6 Identification code FI C08K 3/22 C08K 3/22 3/26 3/26 5/524 5/524 H01L 23/29 H01L 23/30 R 23/31 // (C08L 63/00 23:00) (72) Inventor Terumi Tsukahara 172-1, Okakabo, Yuki-shi, Ibaraki Hitachi Chemical Co., Ltd. Shimodate Plant (72) Inventor Masanobu Fujii 1772- Okakabo, Yuki-shi, Ibaraki 1 Hitachi Chemical Industries Co., Ltd. Shimodate Plant (72) Inventor Hiroki Yukishima 172-1 Okakubo, Yuki City, Ibaraki Prefecture Hitachi Chemical Co., Ltd. Shimodate Plant

Claims (7)

【特許請求の範囲】[Claims] 【請求項1】下記(A)〜(D)成分からなる半導体封
止用エポキシ樹脂組成物。 (A)下記構造式1で表されるエポキシ樹脂を70重量
%以上含有するエポキシ樹脂、 【化1】 (B)1分子中に2個以上のフェノール性水酸基を有す
る化合物、 (C)下記構造式2で表されるリン化合物 【化2】 及び(D)エポキシ樹脂組成物総量中60〜95重量%
の無機充填材。
An epoxy resin composition for semiconductor encapsulation comprising the following components (A) to (D): (A) an epoxy resin containing 70% by weight or more of an epoxy resin represented by the following structural formula 1: (B) a compound having two or more phenolic hydroxyl groups in one molecule; (C) a phosphorus compound represented by the following structural formula 2: And (D) 60 to 95% by weight based on the total amount of the epoxy resin composition
Inorganic filler.
【請求項2】(A)成分が下記構造式3で表されるエポ
キシ樹脂を2〜30重量%含有するエポキシ樹脂である
請求項1記載の半導体封止用エポキシ樹脂組成物。 【化3】 (式中、Rは水素原子または炭素数1〜4の低級アルキ
ル基を表し、mは0〜6の整数を示す。)
2. The epoxy resin composition for semiconductor encapsulation according to claim 1, wherein the component (A) is an epoxy resin containing 2 to 30% by weight of an epoxy resin represented by the following structural formula 3. Embedded image (In the formula, R represents a hydrogen atom or a lower alkyl group having 1 to 4 carbon atoms, and m represents an integer of 0 to 6.)
【請求項3】(B)成分が下記構造式4で表される化合
物である請求項1または2記載の半導体封止用エポキシ
樹脂組成物。 【化4】 (式中、pは0〜6の整数を表す。)
3. The epoxy resin composition for semiconductor encapsulation according to claim 1, wherein the component (B) is a compound represented by the following structural formula 4. Embedded image (In the formula, p represents an integer of 0 to 6.)
【請求項4】酸化若しくは非酸化型のポリオレフィン類
を(A)成分の全エポキシ樹脂100重量部に対し、
0.01〜10重量部含有する請求項1、2又は3に記
載の半導体封止用エポキシ樹脂組成物。
4. An oxidized or non-oxidized polyolefin is added to 100 parts by weight of the total epoxy resin as the component (A).
The epoxy resin composition for semiconductor encapsulation according to claim 1, which contains 0.01 to 10 parts by weight.
【請求項5】難燃剤としてブロム化エポキシ樹脂または
三酸化アンチモンを含有する請求項1乃至4のいずれか
に記載の半導体封止用エポキシ樹脂組成物。
5. The epoxy resin composition for semiconductor encapsulation according to claim 1, which comprises a brominated epoxy resin or antimony trioxide as a flame retardant.
【請求項6】下記式5で表される無機イオン補足剤を含
有する請求項1乃至5のいずれかに記載の半導体封止用
エポキシ樹脂組成物。 Mg4.5 Al2 (OH)13CO3 ・3.5H2 O 式5
6. The epoxy resin composition for semiconductor encapsulation according to claim 1, further comprising an inorganic ion scavenger represented by the following formula (5). Mg 4.5 Al 2 (OH) 13 CO 3 .3.5H 2 O Formula 5
【請求項7】請求項1乃至6のいずれかに記載の半導体
封止用エポキシ樹脂組成物で封止したことを特徴とする
樹脂封止型半導体装置。
7. A resin-encapsulated semiconductor device, which is encapsulated with the epoxy resin composition for encapsulating a semiconductor according to any one of claims 1 to 6.
JP9855197A 1997-04-16 1997-04-16 Epoxy resin composition for semiconductor sealing and semiconductor device sealed therewith Pending JPH10287793A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9855197A JPH10287793A (en) 1997-04-16 1997-04-16 Epoxy resin composition for semiconductor sealing and semiconductor device sealed therewith

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9855197A JPH10287793A (en) 1997-04-16 1997-04-16 Epoxy resin composition for semiconductor sealing and semiconductor device sealed therewith

Publications (1)

Publication Number Publication Date
JPH10287793A true JPH10287793A (en) 1998-10-27

Family

ID=14222834

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9855197A Pending JPH10287793A (en) 1997-04-16 1997-04-16 Epoxy resin composition for semiconductor sealing and semiconductor device sealed therewith

Country Status (1)

Country Link
JP (1) JPH10287793A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SG121779A1 (en) * 2002-06-05 2006-05-26 Sumitomo Bakelite Co Curing accelerator, epoxy resin composition, and semiconductor device
CN116970260A (en) * 2023-09-22 2023-10-31 深圳先进电子材料国际创新研究院 Epoxy plastic package material and preparation method and application thereof

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SG121779A1 (en) * 2002-06-05 2006-05-26 Sumitomo Bakelite Co Curing accelerator, epoxy resin composition, and semiconductor device
US7074738B2 (en) * 2002-06-05 2006-07-11 Sumitomo Bakelite Company Limited Curing accelerator, epoxy resin composition, and semiconductor device
CN116970260A (en) * 2023-09-22 2023-10-31 深圳先进电子材料国际创新研究院 Epoxy plastic package material and preparation method and application thereof
CN116970260B (en) * 2023-09-22 2024-01-23 深圳先进电子材料国际创新研究院 Epoxy plastic package material and preparation method and application thereof

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