Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JP5053930B2 - Epoxy resin composition for semiconductor encapsulation and semiconductor device using the same - Google Patents
[go: Go Back, main page]

JP5053930B2 - Epoxy resin composition for semiconductor encapsulation and semiconductor device using the same - Google Patents

Epoxy resin composition for semiconductor encapsulation and semiconductor device using the same Download PDF

Info

Publication number
JP5053930B2
JP5053930B2 JP2008138340A JP2008138340A JP5053930B2 JP 5053930 B2 JP5053930 B2 JP 5053930B2 JP 2008138340 A JP2008138340 A JP 2008138340A JP 2008138340 A JP2008138340 A JP 2008138340A JP 5053930 B2 JP5053930 B2 JP 5053930B2
Authority
JP
Japan
Prior art keywords
epoxy resin
resin composition
semiconductor
bisphenol
type epoxy
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
JP2008138340A
Other languages
Japanese (ja)
Other versions
JP2009286843A (en
Inventor
照詞 堀井
啓之 白木
隆景 松本
朋史 上村
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.)
Panasonic Corp
Panasonic Holdings Corp
Original Assignee
Panasonic Corp
Matsushita Electric Industrial 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 Panasonic Corp, Matsushita Electric Industrial Co Ltd filed Critical Panasonic Corp
Priority to JP2008138340A priority Critical patent/JP5053930B2/en
Publication of JP2009286843A publication Critical patent/JP2009286843A/en
Application granted granted Critical
Publication of JP5053930B2 publication Critical patent/JP5053930B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

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

Description

本発明は、電気・電子部品、汎用半導体装置、光半導体装置等における半導体を封止するために用いられる半導体封止用エポキシ樹脂組成物およびそれを用いた半導体装置に関するものである。   The present invention relates to an epoxy resin composition for semiconductor encapsulation used for encapsulating semiconductors in electrical / electronic components, general-purpose semiconductor devices, optical semiconductor devices, and the like, and a semiconductor device using the same.

従来より、電気・電子部品、汎用半導体装置、光半導体装置等における半導体の封止材料として、密着性、耐湿性、電気絶縁性、耐熱性、透明性等の点で優れ、大量生産可能なエポキシ樹脂組成物が用いられている(例えば、特許文献1−2参照)。そして近年では半導体の高機能化が進んでより緻密なPKG構造を持つ半導体装置が開発され、それに伴いワイヤーがより細く長くなり、封止材料としては低粘度化した樹脂組成物が要求されている。しかしながら、このような低粘度化した樹脂組成物は、粘度の低下に伴い融点も低下するため封止材料がブロッキングを起こすという問題があった。この問題に対して、現在では、ブロッキングが発生しないように封止材料を適切な温湿度で管理し、ブロッキングが発生した場合には人の手で再粉砕しているのが実情である。
特開2008−74930号公報 特開2007−169493号公報
Conventionally, epoxy that can be mass-produced as a sealing material for semiconductors in electrical / electronic parts, general-purpose semiconductor devices, optical semiconductor devices, etc. in terms of adhesion, moisture resistance, electrical insulation, heat resistance, transparency, etc. A resin composition is used (see, for example, Patent Document 1-2). In recent years, as semiconductors have advanced in functionality, semiconductor devices having a finer PKG structure have been developed. As a result, wires have become thinner and longer, and a resin composition having a reduced viscosity is required as a sealing material. . However, such a low-viscosity resin composition has a problem in that the sealing material causes blocking because the melting point decreases as the viscosity decreases. To solve this problem, at present, the sealing material is managed at an appropriate temperature and humidity so that blocking does not occur, and when blocking occurs, it is actually re-pulverized by human hands.
JP 2008-74930 A JP 2007-169493 A

上記ブロッキング問題は封止材料の粉体加工性および作業性を著しく悪化させるため、安定生産性の観点から低粘度樹脂組成物の開発を困難なものにしている。   Since the blocking problem significantly deteriorates the powder processability and workability of the sealing material, it makes development of a low-viscosity resin composition difficult from the viewpoint of stable productivity.

本発明は、以上のとおりの事情に鑑みてなされたものであり、低粘度かつ耐ブロッキング性に優れた半導体封止用エポキシ樹脂組成物およびそれを用いた半導体装置を提供することを課題としている。   This invention is made | formed in view of the situation as mentioned above, and makes it a subject to provide the epoxy resin composition for semiconductor sealing excellent in the low viscosity and the blocking resistance, and a semiconductor device using the same. .

本発明は、上記の課題を解決するために、以下のことを特徴としている。   The present invention is characterized by the following in order to solve the above problems.

第1に、本発明の半導体封止用エポキシ樹脂組成物は、エポキシ樹脂、硬化剤および無機充填材を必須成分として含有する半導体封止用エポキシ樹脂組成物において、前記エポキシ樹脂は、次式(1)   1stly, the epoxy resin composition for semiconductor sealing of this invention is an epoxy resin composition for semiconductor sealing which contains an epoxy resin, a hardening | curing agent, and an inorganic filler as an essential component, The said epoxy resin is following Formula ( 1)

Figure 0005053930
Figure 0005053930

で表される構造のビスフェノールF型エポキシ樹脂を含み、前記ビスフェノールF型エポキシ樹脂は、エポキシ樹脂組成物全量に対して2〜15質量%の割合で配合され、かつ、エポキシ樹脂全量に対して25〜100質量%の割合で含有し、前記硬化剤は、フェノールノボラック樹脂とビフェニルアラルキル樹脂とを含むことを特徴とする。 In look-containing bisphenol F type epoxy resin having a structure represented, the bisphenol F type epoxy resin is blended in an amount of 2 to 15% by weight relative to the epoxy resin composition the total amount, and the epoxy resin the total amount in a proportion of 25 to 100 wt%, wherein the curing agent is characterized in containing Mukoto a phenol novolak resin and biphenyl aralkyl resin.

第2に、半導体装置として、第1の半導体封止用エポキシ樹脂組成物の硬化体で半導体素子が封止されていることを特徴とする。   Second, as a semiconductor device, a semiconductor element is sealed with a cured body of the first semiconductor sealing epoxy resin composition.

上記第1の発明によれば、エポキシ樹脂、硬化剤および無機充填材を必須成分として含有する半導体封止用エポキシ樹脂組成物において、前記エポキシ樹脂は、前記式(1)で表される構造のビスフェノールF型エポキシ樹脂を含むことにより、低粘度化を実現しつつブロッキングを抑制することができる。これによって粉体加工性および作業性がより容易になり、かつ高い成形性を有し、生産性を効果的に向上させることができる。   According to the first invention, in the epoxy resin composition for semiconductor encapsulation containing an epoxy resin, a curing agent and an inorganic filler as essential components, the epoxy resin has a structure represented by the formula (1). By including a bisphenol F-type epoxy resin, blocking can be suppressed while realizing a low viscosity. As a result, the powder processability and workability become easier, and the moldability is high, and the productivity can be effectively improved.

以上のような顕著な効果は、上記第2の発明の半導体装置として実際上大きく実現され、ワイヤーがより細く長い半導体装置であっても良好な品質のものを得ることができる。   The remarkable effects as described above are practically realized as the semiconductor device according to the second aspect of the present invention, and even a semiconductor device having a finer and longer wire can be obtained with good quality.

本発明は前記のとおりの特徴をもつものであるが、以下に、本発明を実施するための最良の形態を説明する。   The present invention has the features as described above, and the best mode for carrying out the present invention will be described below.

本発明の半導体封止用エポキシ樹脂組成物(以下、単に「エポキシ樹脂組成物」ともいう)は、エポキシ樹脂、硬化剤および無機充填材を必須成分とする。   The epoxy resin composition for semiconductor encapsulation of the present invention (hereinafter also simply referred to as “epoxy resin composition”) contains an epoxy resin, a curing agent and an inorganic filler as essential components.

本発明に使用されるエポキシ樹脂は、必須成分として前記式(1)で表される構造のビスフェノールF型エポキシ樹脂を含んでおり、これによってエポキシ樹脂組成物の低粘度化を実現し、さらにブロッキングを抑制することができるのである。この前記式(1)で表される構造のビスフェノールF型エポキシ樹脂は市販品または合成されたものであってもよく、後述する実施例では東都化成(株)製のYSLV−80XYを用いている。   The epoxy resin used in the present invention contains a bisphenol F-type epoxy resin having a structure represented by the formula (1) as an essential component, thereby realizing a low viscosity of the epoxy resin composition and further blocking. Can be suppressed. The bisphenol F type epoxy resin having the structure represented by the formula (1) may be a commercially available product or a synthesized one. In the examples described later, YSLV-80XY manufactured by Toto Kasei Co., Ltd. is used. .

前記エポキシ樹脂は、例えばエポキシ樹脂組成物全量に対して2〜15質量%、特に6〜15質量%の割合で配合される。前記式(1)で表される構造のビスフェノールF型エポキシ樹脂は、エポキシ樹脂組成物におけるエポキシ樹脂の全部として、またはその一部として他のエポキシ樹脂とともに用いられ、例えばエポキシ樹脂全量に対して25〜100質量%の割合で含有される。前記式(1)で表される構造のビスフェノールF型エポキシ樹脂が過少である場合には、そのビスフェノールF型エポキシ樹脂の効果を十分に発揮できず、エポキシ樹脂組成物の低粘度化やブロッキングを抑制できない場合がある。   The said epoxy resin is mix | blended, for example in the ratio of 2-15 mass% with respect to the epoxy resin composition whole quantity, especially 6-15 mass%. The bisphenol F-type epoxy resin having the structure represented by the above formula (1) is used together with other epoxy resins as the entire epoxy resin in the epoxy resin composition or as a part thereof, for example, 25 It is contained at a ratio of ˜100% by mass. When the bisphenol F type epoxy resin having the structure represented by the formula (1) is too small, the effect of the bisphenol F type epoxy resin cannot be sufficiently exhibited, and the viscosity of the epoxy resin composition is reduced or blocked. It may not be possible to suppress it.

前記式(1)で表される構造のビスフェノールF型エポキシ樹脂とともに用いられる他のエポキシ樹脂としては、一般的に半導体封止用として使用される各種のエポキシ樹脂であってよく、特に限定されない。例えば、ビフェニル型エポキシ樹脂、フェノールノボラック型エポキシ樹脂、クレゾールノボラック型エポキシ樹脂、前記式(1)で表される構造のビスフェノールF型エポキシ樹脂以外のビスフェノール型エポキシ樹脂、スチルベン型エポキシ樹脂、トリフェノールメタン型エポキシ樹脂、フェノールアラルキル型エポキシ樹脂、ナフトール型エポキシ樹脂、ナフタレン型エポキシ樹脂等を挙げることができる。これらは1種に限定されず、複数種を組み合わせて使用してもよい。特に耐ブロッキング性の観点からはビフェニルアラルキル型エポキシ樹脂を併用することが望ましい。   The other epoxy resin used together with the bisphenol F-type epoxy resin having the structure represented by the formula (1) may be various epoxy resins generally used for semiconductor encapsulation, and is not particularly limited. For example, biphenyl type epoxy resin, phenol novolac type epoxy resin, cresol novolac type epoxy resin, bisphenol type epoxy resin other than bisphenol F type epoxy resin having the structure represented by the above formula (1), stilbene type epoxy resin, triphenolmethane Type epoxy resin, phenol aralkyl type epoxy resin, naphthol type epoxy resin, naphthalene type epoxy resin and the like. These are not limited to one type, and a plurality of types may be used in combination. In particular, from the viewpoint of blocking resistance, it is desirable to use a biphenyl aralkyl type epoxy resin in combination.

本発明において使用される硬化剤は、エポキシ樹脂と反応するフェノール性水酸基を有する樹脂であれば特に限定されない。具体的には、フェノールノボラック樹脂、クレゾールノボラック樹脂、フェノールアラルキル樹脂、ビフェニルアラルキル樹脂、ナフトールアラルキル樹脂等のナフタレン骨格含有フェノール樹脂等、各種の多価フェノール化合物やナフトール化合物が例示される。これらは1種に限定されず、複数種を組み合わせて使用してもよい。フェノール性水酸基を有する樹脂の含有量は特に限定されないが、例えば、エポキシ樹脂とフェノール性水酸基を有する樹脂との当量比(OH当量/エポキシ当量)が0.5〜1.5の範囲、好ましくは0.8〜1.2の範囲となるように配合することができる。当量比が0.5〜1.5の範囲外であると、エポキシ樹脂組成物の硬化特性が低下したり、成形後の硬化物の耐湿性が低下する場合がある。   The curing agent used in the present invention is not particularly limited as long as it is a resin having a phenolic hydroxyl group that reacts with an epoxy resin. Specific examples include various polyhydric phenol compounds and naphthol compounds such as phenol novolak resins, cresol novolak resins, phenol aralkyl resins, biphenyl aralkyl resins, and naphthol skeleton-containing phenol resins such as naphthol aralkyl resins. These are not limited to one type, and a plurality of types may be used in combination. The content of the resin having a phenolic hydroxyl group is not particularly limited. For example, the equivalent ratio of the epoxy resin to the resin having a phenolic hydroxyl group (OH equivalent / epoxy equivalent) is in the range of 0.5 to 1.5, preferably It can mix | blend so that it may become the range of 0.8-1.2. If the equivalent ratio is outside the range of 0.5 to 1.5, the curing characteristics of the epoxy resin composition may be reduced, or the moisture resistance of the cured product after molding may be reduced.

本発明に使用される無機充填材としては、一般的に半導体封止用として使用されるものであればよく、その種類は特に限定されない。例えば、溶融シリカ、結晶シリカ、アルミナ、窒化ケイ素、窒化アルミニウム等が挙げられる。無機充填材の含有量も特に限定されないが、例えば、エポキシ樹脂組成物全量に対して80〜93質量%とすることができる。これによってエポキシ樹脂組成物の吸湿性を効果的に低下させ、耐リフロークラック性を向上させることができる。無機充填材の配合量が過少であると、熱伝導性、熱膨張率等の特性が低下する場合がある。逆に過剰であると、成形時の流動性と金型充填性が低下する場合がある。   The inorganic filler used in the present invention is not particularly limited as long as it is generally used for semiconductor encapsulation. Examples thereof include fused silica, crystalline silica, alumina, silicon nitride, and aluminum nitride. Although content of an inorganic filler is not specifically limited, For example, it can be 80-93 mass% with respect to the epoxy resin composition whole quantity. This effectively reduces the hygroscopicity of the epoxy resin composition and improves the reflow crack resistance. If the amount of the inorganic filler is too small, characteristics such as thermal conductivity and coefficient of thermal expansion may be deteriorated. On the other hand, if it is excessive, fluidity and mold filling property during molding may be deteriorated.

また本発明のエポキシ樹脂組成物は、エポキシ樹脂の硬化反応を促進させるために硬化促進剤を含有することが望ましい。硬化促進剤としては、エポキシ基とフェノール性水酸基の反応を促進するものであれば特に限定されない。例えば、テトラフェニルホスホニウム・テトラフェニルボレートやトリフェニルホスフィン等の有機ホスフィン類、ジアザビシクロウンデセン等の三級アミン類、2−メチルイミダゾール、2−フェニルイミダゾール等のイミダゾール類が挙げられる。これらは1種に限定されず、複数種を組み合わせて使用してもよい。   Moreover, in order for the epoxy resin composition of this invention to accelerate | stimulate the hardening reaction of an epoxy resin, it is desirable to contain a hardening accelerator. The curing accelerator is not particularly limited as long as it accelerates the reaction between the epoxy group and the phenolic hydroxyl group. Examples thereof include organic phosphines such as tetraphenylphosphonium / tetraphenylborate and triphenylphosphine, tertiary amines such as diazabicycloundecene, and imidazoles such as 2-methylimidazole and 2-phenylimidazole. These are not limited to one type, and a plurality of types may be used in combination.

さらに本発明のエポキシ樹脂組成物は、本発明の効果を損なわない範囲内において、上記以外の成分を配合することができる。例えば、γ−アミノプロピルトリエトキシシランやN−フェニル−γ−アミノプロピルトリメトキシシラン等のアミノシラン、γ−メルカプトプロピルトリメトキシシラン等のメルカプトシラン、γ−グリシドキシプロピルトリメトキシシラン等のグリシドキシシラン等のシランカップリング剤、三酸化アンチモン等の難燃剤、カーボンブラック等の着色剤、シリコーン可とう剤等が挙げられる。また、カルナバワックス、脂肪酸アミド、ステアリン酸、モンタン酸、脂肪酸エステル、カルボキシル基含有ポリオレフィン等の離型剤が配合されていてもよい。   Furthermore, the epoxy resin composition of this invention can mix | blend components other than the above in the range which does not impair the effect of this invention. For example, aminosilanes such as γ-aminopropyltriethoxysilane and N-phenyl-γ-aminopropyltrimethoxysilane, mercaptosilanes such as γ-mercaptopropyltrimethoxysilane, and glycids such as γ-glycidoxypropyltrimethoxysilane Examples include silane coupling agents such as xysilane, flame retardants such as antimony trioxide, colorants such as carbon black, and silicone flexible agents. Moreover, mold release agents, such as carnauba wax, fatty acid amide, stearic acid, montanic acid, fatty acid ester, and carboxyl group-containing polyolefin, may be blended.

以上のとおりの本発明の半導体封止用エポキシ樹脂組成物は、前記式(1)で表される構造のビスフェノールF型エポキシ樹脂を含むエポキシ樹脂、硬化剤および無機充填材、さらに必要に応じて各種の添加剤を配合し、これをミキサーやブレンダーで均一に混合した後に、加熱ロールやニーダー等で混練することによって調製できる。ここで上記の各成分の配合順序は特に限定されるものではない。また混練物を必要に応じて冷却固化し、粉砕してペレットやパウダーにしたり、あるいはタブレット化したりして使用することができる。ここで得られたペレット、パウダー、タブレット等の半導体封止用エポキシ樹脂組成物は、耐ブロッキング性に優れたものとなる。   The epoxy resin composition for semiconductor encapsulation of the present invention as described above includes an epoxy resin containing a bisphenol F type epoxy resin having a structure represented by the above formula (1), a curing agent and an inorganic filler, and further if necessary. It can be prepared by blending various additives, uniformly mixing them with a mixer or blender, and then kneading them with a heating roll or kneader. Here, the blending order of the above components is not particularly limited. Further, the kneaded product can be cooled and solidified as necessary, pulverized into pellets or powder, or tableted and used. The epoxy resin composition for semiconductor encapsulation such as pellets, powders and tablets obtained here is excellent in blocking resistance.

そして、このようにして調製した半導体封止用エポキシ樹脂組成物を用いて封止成形することによって、半導体装置を作製することができる。例えば、IC等の半導体素子を搭載したリードフレームをトランスファー成形金型にセットし、トランスファー成形を行うことによって、半導体素子を半導体封止用エポキシ樹脂組成物で封止した半導体装置を作製する。   And a semiconductor device can be produced by carrying out sealing molding using the epoxy resin composition for semiconductor sealing prepared in this way. For example, a lead frame on which a semiconductor element such as an IC is mounted is set in a transfer molding die, and transfer molding is performed to manufacture a semiconductor device in which the semiconductor element is sealed with an epoxy resin composition for semiconductor sealing.

以下、実施例を示し、この発明の実施の形態についてさらに詳しく説明する。もちろん、この発明は以下の例に限定されるものではなく、細部については様々な態様が可能であることは言うまでもない。   Hereinafter, an example is shown and an embodiment of this invention is described in more detail. Of course, the present invention is not limited to the following examples, and it goes without saying that various aspects are possible in detail.

<実施例1〜5および比較例1〜4>
表1に示す配合量で各成分を配合し、ブレンダーで30分間混合して均一化した後、80℃に加熱した2本ロールで混練溶融させて押し出し、冷却した後、粉砕機で所定粒度に粉砕して粉粒状(パウダー状)の半導体封止用エポキシ樹脂組成物を得た。
<Examples 1-5 and Comparative Examples 1-4>
Each component is blended in the blending amounts shown in Table 1, mixed for 30 minutes with a blender, homogenized, kneaded and melted with two rolls heated to 80 ° C., extruded, cooled, and then adjusted to a predetermined particle size with a pulverizer. The pulverized epoxy resin composition for semiconductor encapsulation was obtained by pulverization.

なお、表1におけるエポキシ樹脂組成物の配合材料としては、下記のものを用いた。
エポキシ樹脂1:前記式(1)で表される構造のビスフェノールF型エポキシ樹脂(東都化成(株) YSLV−80XY)
エポキシ樹脂2:ビフェニル型エポキシ樹脂(ジャパンエポキシレジン(株) YX4000H)
エポキシ樹脂3:ビフェニル型エポキシ樹脂(ジャパンエポキシレジン(株) YL−6121H)
エポキシ樹脂4:ビスフェノールA型エポキシ樹脂(ジャパンエポキシレジン(株) YL−6810)
硬化剤1:フェノールノボラック樹脂(明和化成(株)製 DL92)
硬化剤2:フェノールノボラック樹脂(明和化成(株)製 DL65)
硬化剤3:ビフェニルアラルキル樹脂(明和化成(株) MEH7851SS)
無機充填材:溶融シリカ(電気化学工業(株)製、FB940)
カップリング剤:信越化学工業(株)製、KBM8020
離型剤:カルナバワックス(大日化学(株)製、F1−100)
着色剤:カーボンブラック(三菱化学(株)製 MA600MJ)
硬化促進剤1:明和化成(株)製 KXM
硬化促進剤2:四国化成(株)製 2P4MHZ
上記粉粒状の半導体封止用エポキシ樹脂組成物の評価方法は下記のとおりである。
<スリット粘度(Pa・s)の測定>
矩形粘度測定機(松下電工(株)製)を用いてスリット粘度を測定した。幅W、厚さDの長尺スリットの上流側と下流側にそれぞれ圧力センサS、Sを設け(センサ間距離L)、金型温度を175℃として注入圧:10MPa、注入速度Q:1.3mm/s、ポット保持時間:10sの条件で圧力センサSの上流からスリット内に半導体封止用エポキシ樹脂組成物を注入してスリット内を通過させ、圧力センサS、Sにより圧力損失ΔPを測定し、下記式からスリット粘度η(Pa・s)を求めた。
In addition, as a compounding material of the epoxy resin composition in Table 1, the following were used.
Epoxy resin 1: Bisphenol F-type epoxy resin having the structure represented by the above formula (1) (Tosuto Kasei Co., Ltd. YSLV-80XY)
Epoxy resin 2: biphenyl type epoxy resin (Japan Epoxy Resin Co., Ltd. YX4000H)
Epoxy resin 3: biphenyl type epoxy resin (Japan Epoxy Resin Co., Ltd. YL-6121H)
Epoxy resin 4: bisphenol A type epoxy resin (Japan Epoxy Resin Co., Ltd. YL-6810)
Hardener 1: Phenol novolac resin (DL92 manufactured by Meiwa Kasei Co., Ltd.)
Curing agent 2: Phenol novolac resin (DL65 manufactured by Meiwa Kasei Co., Ltd.)
Curing agent 3: biphenyl aralkyl resin (Maywa Kasei Co., Ltd. MEH7851SS)
Inorganic filler: fused silica (manufactured by Denki Kagaku Kogyo Co., Ltd., FB940)
Coupling agent: Shin-Etsu Chemical Co., Ltd., KBM8020
Mold release agent: Carnauba wax (F1-100, manufactured by Dainichi Chemical Co., Ltd.)
Colorant: Carbon Black (MA600MJ manufactured by Mitsubishi Chemical Corporation)
Curing accelerator 1: KXM manufactured by Meiwa Kasei Co., Ltd.
Curing accelerator 2: Shikoku Kasei Co., Ltd. 2P4MHZ
The evaluation method of the above-mentioned powdery epoxy resin composition for encapsulating a semiconductor is as follows.
<Measurement of slit viscosity (Pa · s)>
The slit viscosity was measured using a rectangular viscometer (manufactured by Matsushita Electric Works Co., Ltd.). Pressure sensors S 1 and S 2 are provided on the upstream side and the downstream side of the long slit of width W and thickness D (distance L between sensors), the mold temperature is set to 175 ° C., injection pressure: 10 MPa, injection speed Q: 1.3 mm / s, the pot holding time under conditions of 10s by implanting the semiconductor encapsulating epoxy resin composition into the slit from the upstream of the pressure sensor S 1 was allowed to pass through the slit, by the pressure sensor S 1, S 2 The pressure loss ΔP was measured, and the slit viscosity η (Pa · s) was determined from the following formula.

ΔP=(12η/WD)QL
<ブロッキング性評価>
上記粉粒状の半導体封止用エポキシ樹脂組成物3kgを25℃(シリカゲル入り)環境下で24h放置し、その後ブロッキング量を計量し、試験に供した半導体封止用エポキシ樹脂組成物の全量に対するブロッキング量からブロッキング率(%)を求めた。
ΔP = (12η / WD 3 ) QL
<Evaluation of blocking properties>
3 kg of the above-mentioned powdery epoxy resin composition for encapsulating semiconductors is allowed to stand in an environment of 25 ° C. (with silica gel) for 24 hours, and then the blocking amount is measured to block the total amount of the epoxy resin composition for semiconductor encapsulation used in the test. The blocking rate (%) was determined from the amount.

結果を表1に示す。   The results are shown in Table 1.

Figure 0005053930
Figure 0005053930

表1にみられるように、前記式(1)で表される構造のビスフェノールF型エポキシ樹脂を含むエポキシ樹脂、硬化剤および無機充填材を必須成分として含有する半導体封止用エポキシ樹脂組成物(実施例1〜5)は、低粘度でかつ耐ブロッキング性に優れていることが確認できた。   As seen in Table 1, an epoxy resin composition for semiconductor encapsulation containing an epoxy resin containing a bisphenol F-type epoxy resin having a structure represented by the formula (1), a curing agent and an inorganic filler as essential components ( Examples 1 to 5) were confirmed to have low viscosity and excellent blocking resistance.

他方、前記式(1)で表される構造のビスフェノールF型エポキシ樹脂を用いていない半導体封止用エポキシ樹脂組成物(比較例1〜4)は、低粘度化および耐ブロッキング性のうちの少なくともいずれかを実現することができないことが確認できた。   On the other hand, the epoxy resin composition for semiconductor encapsulation that does not use the bisphenol F-type epoxy resin having the structure represented by the formula (1) (Comparative Examples 1 to 4) is at least one of low viscosity and blocking resistance. It was confirmed that either could not be realized.

Claims (2)

エポキシ樹脂、硬化剤および無機充填材を必須成分として含有する半導体封止用エポキシ樹脂組成物において、前記エポキシ樹脂は、次式(1)
Figure 0005053930
で表される構造のビスフェノールF型エポキシ樹脂を含み、前記ビスフェノールF型エポキシ樹脂は、エポキシ樹脂組成物全量に対して2〜15質量%の割合で配合され、かつ、エポキシ樹脂全量に対して25〜100質量%の割合で含有し、前記硬化剤は、フェノールノボラック樹脂とビフェニルアラルキル樹脂とを含むことを特徴とする半導体封止用エポキシ樹脂組成物。
In the epoxy resin composition for semiconductor encapsulation containing an epoxy resin, a curing agent and an inorganic filler as essential components, the epoxy resin has the following formula (1):
Figure 0005053930
In look-containing bisphenol F type epoxy resin having a structure represented, the bisphenol F type epoxy resin is blended in an amount of 2 to 15% by weight relative to the epoxy resin composition the total amount, and the epoxy resin the total amount in a proportion of 25 to 100 wt%, wherein the curing agent is a semiconductor encapsulating epoxy resin composition characterized contains Mukoto a phenol novolak resin and biphenyl aralkyl resin.
請求項1に記載の半導体封止用エポキシ樹脂組成物の硬化体で半導体素子が封止されていることを特徴とする半導体装置。   A semiconductor device, wherein a semiconductor element is sealed with a cured body of the epoxy resin composition for semiconductor sealing according to claim 1.
JP2008138340A 2008-05-27 2008-05-27 Epoxy resin composition for semiconductor encapsulation and semiconductor device using the same Active JP5053930B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2008138340A JP5053930B2 (en) 2008-05-27 2008-05-27 Epoxy resin composition for semiconductor encapsulation and semiconductor device using the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2008138340A JP5053930B2 (en) 2008-05-27 2008-05-27 Epoxy resin composition for semiconductor encapsulation and semiconductor device using the same

Publications (2)

Publication Number Publication Date
JP2009286843A JP2009286843A (en) 2009-12-10
JP5053930B2 true JP5053930B2 (en) 2012-10-24

Family

ID=41456390

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008138340A Active JP5053930B2 (en) 2008-05-27 2008-05-27 Epoxy resin composition for semiconductor encapsulation and semiconductor device using the same

Country Status (1)

Country Link
JP (1) JP5053930B2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4617387B2 (en) * 2009-06-17 2011-01-26 キヤノン株式会社 Manufacturing method of fine structure
JP2014118461A (en) * 2012-12-14 2014-06-30 Kyocera Chemical Corp Resin composition for granular semiconductor sealing and semiconductor device
JP6351927B2 (en) * 2012-12-27 2018-07-04 京セラ株式会社 Resin composition for sealing and method for manufacturing semiconductor device
JPWO2023140256A1 (en) * 2022-01-18 2023-07-27

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006028264A (en) * 2004-07-13 2006-02-02 Hitachi Chem Co Ltd Epoxy resin molding material for sealing and electronic component device
JP4792768B2 (en) * 2005-03-02 2011-10-12 日立化成工業株式会社 Epoxy resin composition for sealing and electronic component device
JP2007002206A (en) * 2005-05-24 2007-01-11 Hitachi Chem Co Ltd Epoxy resin composition for sealing and electronic part device
JP2007009166A (en) * 2005-06-03 2007-01-18 Hitachi Chem Co Ltd Epoxy resin composition for sealing, and electronic component apparatus
JP4930767B2 (en) * 2006-08-21 2012-05-16 日立化成工業株式会社 Epoxy resin composition for sealing and electronic component device
JP5141132B2 (en) * 2006-08-31 2013-02-13 住友ベークライト株式会社 Epoxy resin composition for semiconductor encapsulation and semiconductor device

Also Published As

Publication number Publication date
JP2009286843A (en) 2009-12-10

Similar Documents

Publication Publication Date Title
JP2012224758A (en) Epoxy resin composition and semiconductor device
JP2013119588A (en) Epoxy resin composition for sealing electronic component and electronic component device using the same
JP2016040383A (en) Epoxy resin composition for electronic component sealing and electronic component device using the same
JP5053930B2 (en) Epoxy resin composition for semiconductor encapsulation and semiconductor device using the same
JP4950010B2 (en) Manufacturing method of epoxy resin composition for semiconductor encapsulation and manufacturing method of semiconductor device
JP2005213299A (en) Semiconductor sealing resin composition and semiconductor device using the same
JP2002309067A (en) Epoxy resin composition for sealing and semiconductor device
JP5938741B2 (en) Epoxy resin composition for sealing, method for producing the same, and semiconductor device
JP2009007405A (en) Epoxy resin composition for semiconductor encapsulation and semiconductor device
JP5226387B2 (en) Epoxy resin composition for semiconductor encapsulation and semiconductor device
JP5547680B2 (en) Epoxy resin composition for sealing and semiconductor device
JP5102095B2 (en) Semiconductor-encapsulated epoxy resin composition for compression molding and semiconductor device using the same
JP2010031119A (en) Semiconductor-sealing epoxy resin composition and semiconductor device using it
JP2002194064A (en) Resin composition for semiconductor encapsulation, and semiconductor device using the same
JP2009286841A (en) Epoxy resin composition for encapsulation and semiconductor device
JP2010195880A (en) Epoxy resin composition for sealing semiconductor and semiconductor device using the composition
JP4946030B2 (en) Epoxy resin composition and semiconductor device
JP3417283B2 (en) Epoxy resin composition for sealing and semiconductor device sealing method
JP2009173812A (en) Epoxy resin composition for sealing and semiconductor device
JP2005179585A (en) Epoxy resin composition for use in sealing semiconductor, and semiconductor device
JP3804614B2 (en) Epoxy resin composition for semiconductor encapsulation and semiconductor device
JP2012025906A (en) Epoxy resin composition for sealing semiconductor and semiconductor device using the same
JP2014019717A (en) Semiconductor sealing epoxy resin composition and semiconductor device
JP2012111844A (en) Epoxy resin composition for sealing, and semiconductor device sealed using the same
JP2008156403A (en) Epoxy resin composition for sealing semiconductor, and semiconductor device

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20090925

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20110921

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20110927

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20111128

A711 Notification of change in applicant

Free format text: JAPANESE INTERMEDIATE CODE: A712

Effective date: 20120111

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20120703

A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20120726

R150 Certificate of patent or registration of utility model

Ref document number: 5053930

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

Free format text: JAPANESE INTERMEDIATE CODE: R150

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20150803

Year of fee payment: 3