JPH0651786B2 - Epoxy resin composition for semiconductor device encapsulation - Google Patents
Epoxy resin composition for semiconductor device encapsulationInfo
- Publication number
- JPH0651786B2 JPH0651786B2 JP60214622A JP21462285A JPH0651786B2 JP H0651786 B2 JPH0651786 B2 JP H0651786B2 JP 60214622 A JP60214622 A JP 60214622A JP 21462285 A JP21462285 A JP 21462285A JP H0651786 B2 JPH0651786 B2 JP H0651786B2
- Authority
- JP
- Japan
- Prior art keywords
- epoxy resin
- resin
- component
- amount
- silica powder
- 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.)
- Expired - Lifetime
Links
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L23/00—Details of semiconductor or other solid state devices
- H01L23/28—Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection
- H01L23/29—Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection characterised by the material, e.g. carbon
- H01L23/293—Organic, e.g. plastic
- H01L23/295—Organic, e.g. plastic containing a filler
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
- H01L2924/0001—Technical content checked by a classifier
- H01L2924/0002—Not covered by any one of groups H01L24/00, H01L24/00 and H01L2224/00
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- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Epoxy Resins (AREA)
- Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
【発明の詳細な説明】 [発明の技術分野] 本発明は、半導体封止用エポキシ樹脂組成物に関し、更
に詳しくは、優れた耐熱衝撃性及び成形性を有する硬化
物を与える半導体封止用エポキシ樹脂組成物に関する。Description: TECHNICAL FIELD OF THE INVENTION The present invention relates to an epoxy resin composition for semiconductor encapsulation, and more specifically, an epoxy resin for semiconductor encapsulation that gives a cured product having excellent thermal shock resistance and moldability. It relates to a resin composition.
[発明の技術的背景とその問題点] 近年、半導体装置の封止に関する分野においては、半導
体素子の高集積化に伴って、素子上の各種機能単位の細
密化、素子ペレット自体の大型化が急速に進んでいる。
これらの素子ペレットの変化により封止用樹脂も従来の
封止用樹脂では耐熱衝撃性等の要求が満足できなくなっ
てきた。従来、半導体装置の封止用樹脂として用いられ
ている、フェノールノボラック樹脂で硬化させたエポキ
シ樹脂組成物は吸湿性、高温電気特性、成形性などがす
ぐれ、モールド用樹脂の主流となっている。[Technical background of the invention and its problems] In recent years, in the field of semiconductor device encapsulation, along with high integration of semiconductor elements, miniaturization of various functional units on elements and increase in size of element pellets themselves have been required. It is progressing rapidly.
Due to these changes in the element pellets, conventional sealing resins have become unable to satisfy the requirements for thermal shock resistance and the like. Conventionally, an epoxy resin composition cured with a phenol novolac resin, which has been used as a resin for sealing a semiconductor device, has excellent hygroscopicity, high-temperature electrical characteristics, moldability, and the like, and has become the mainstream of molding resins.
しかし、この系統の樹脂組成物を用いて大型でかつ微細
な表面構造を有する素子ペレットを封止すると、素子ペ
レット表面のアルミニウム(Al)パターンを保護するた
めの被覆材であるリンケイ酸ガラス(PSG)膜や窒化ケ
イ素(SIN)膜に割れを生じたり、素子ペレットに割れ
を生じたりする。特に冷熱サイクル試験を実施した場合
に、その傾向が非常に大きい。その結果、ペレット割れ
による素子特性の不良や該膜の割れに起因するAlパター
ンの腐食による不良などを生じる。However, when encapsulating a device pellet having a large and fine surface structure using this type of resin composition, phosphosilicate glass (PSG), which is a coating material for protecting the aluminum (Al) pattern on the device pellet surface, is used. ) The film or silicon nitride (SIN) film is cracked or the element pellet is cracked. This tendency is very large especially when a thermal cycle test is carried out. As a result, defective element characteristics due to pellet cracking, and defective Al pattern corrosion due to cracks in the film occur.
その対策としては、封止樹脂の内部封入物に対する応力
を小さくし、かつ封止樹脂と素子上のPSG膜やSiN膜など
がガラス膜との密着性を大きくする必要がある。As a countermeasure, it is necessary to reduce the stress of the encapsulating resin on the internal inclusions and to increase the adhesion between the encapsulating resin and the PSG film or SiN film on the element with the glass film.
例えば、封止樹脂の内部封入物に対する応力を小さくす
るため、充填剤量を増加させることにより、樹脂の熱膨
張率を低下させる方法がとられている。しかし、この場
合、多量の充填剤使用により、溶融時における粘度の著
しい上昇を招くため樹脂の成形性を損なうという問題が
あった。For example, in order to reduce the stress of the sealing resin with respect to the internal inclusions, a method of decreasing the thermal expansion coefficient of the resin by increasing the amount of the filler is used. However, in this case, there is a problem in that the use of a large amount of the filler causes a remarkable increase in the viscosity during melting, which impairs the moldability of the resin.
さらにこれらの素子ペレットの変化と共に、チップに及
ぼす樹脂及びフィラーの局部応力が原因と思われる信頼
性の低下が問題となってきており、これの回避には、破
砕状フィラーの粗粒をカットすることが有効でると考え
られる。また、パッケージが小型,薄形である場合、成
形金型のゲートは通常のものよりせまいため、この場合
も、大きな破砕状フィラー粒子の存在は好ましくない。
しかしながら、これらの目的で、フィラーの平均粒径を
小さくした場合にも樹脂の溶融粘度が増して、未充填や
ボンディングワイヤの変形を生ずる可能性がある。そこ
で、素子へのダメージが小さく、良好な流動性を持つ球
状のフィラーが注目されているが、単一の粒度分布を持
つ球状フィラーを使った場合、成形時に生ずるバリが著
しく長くなるとともに強度が低下するという欠点があっ
た。Furthermore, along with changes in these element pellets, a decrease in reliability, which is thought to be caused by the local stress of the resin and filler exerted on the chip, has become a problem, and in order to avoid this, cut coarse particles of crushed filler. Is thought to be effective. Further, when the package is small and thin, the gate of the molding die is smaller than that of a normal one, and in this case also, the presence of large crushed filler particles is not preferable.
However, even if the average particle diameter of the filler is reduced for these purposes, the melt viscosity of the resin may increase, and unfilling or deformation of the bonding wire may occur. Therefore, attention has been paid to spherical fillers that have small fluid damage and good flowability, but when spherical fillers with a single particle size distribution are used, burrs that occur during molding become significantly longer and the strength increases. It had the drawback of falling.
[発明の目的] 本発明の目的は、上記した問題点を解消し、優れた耐熱
衝撃性及び成形性を有する硬化物を与える半導体封止用
エポキシ樹脂組成物を提供することにある。[Object of the Invention] An object of the present invention is to provide an epoxy resin composition for semiconductor encapsulation, which solves the above-mentioned problems and gives a cured product having excellent thermal shock resistance and moldability.
[発明の概要] 本発明者らは、上記目的を達成するため、鋭意研究の結
果、通常、充填剤として用いられる破砕状のシリカ粉
に、粒径を考慮した特定の球状シリカ粉を所定量混合し
た半導体封止樹脂が、耐熱衝撃性に優れ、良好な成形性
を持つことを見出し、本発明を完成するに至った。[Summary of the Invention] In order to achieve the above-mentioned object, the present inventors have earnestly studied, and as a result, in a crushed silica powder usually used as a filler, a predetermined amount of a specific spherical silica powder in consideration of a particle size is specified. The inventors have found that the mixed semiconductor encapsulating resin has excellent thermal shock resistance and good moldability, and completed the present invention.
すなわち、本発明の半導体装置封止用エポキシ樹脂組成
物は、 (A)エポキシ樹脂; (B)フェノール樹脂硬化剤; (C)硬化促進剤; (D)平均粒子径3〜100μmを有する破砕状シリカ
粉; (E)平均粒子径1〜50μmを有する球状シリカ粉;及
び (F)エポキシシランと純水からなり、その重量比が9:
1〜9.95:0.05である界面処理剤を、(D)及び(E)成
分の合計量に対して0.1〜1.5重量% を含み、(E)成分の配合量が(D)及び(E)成分の
総配合量に対して5〜90容量%であり、かつ(D)及び
(E)成分の合計量が(A),(B),(C),(D)
及び(E)の合計量に対して50〜75容量%であることを
特徴とするものである。That is, the epoxy resin composition for semiconductor device encapsulation of the present invention comprises: (A) epoxy resin; (B) phenol resin curing agent; (C) curing accelerator; (D) crushed particles having an average particle size of 3 to 100 μm. Silica powder; (E) Spherical silica powder having an average particle size of 1 to 50 μm; and (F) Epoxysilane and pure water, the weight ratio of which is 9:
The surface treatment agent is 1 to 9.95: 0.05 in an amount of 0.1 to 1.5% by weight based on the total amount of the components (D) and (E), and the blending amount of the component (E) is the components (D) and (E). 5 to 90% by volume with respect to the total compounding amount of (D) and (E) and the total amount of (A), (B), (C), (D)
And 50 to 75% by volume with respect to the total amount of (E).
本発明の(A)成分であるエポキシ樹脂は、1分子中に
エポキシ基を少なくとも2個含有するものであれば、い
かなるものであってもよく、例えば、ビスフェノールA
型エポキシ樹脂、ノボラック型エポキシ樹脂、脂環型エ
ポキシ樹脂、グリシジルエステル型エポキシ樹脂が挙げ
られ、これらは単独あるいは2種以上の混合糸で使用さ
れる。The epoxy resin which is the component (A) of the present invention may be any one as long as it contains at least two epoxy groups in one molecule, for example, bisphenol A.
Type epoxy resin, novolac type epoxy resin, alicyclic epoxy resin, glycidyl ester type epoxy resin, and these are used alone or in a mixture of two or more kinds.
本発明の(B)成分であるフェノール樹脂硬化剤は、一
般にエポキシ樹脂の硬化剤として知られているものであ
ればいかなるものであってもよく、例えば、フェノール
ノボラック樹脂、クレゾールノボラック樹脂などのフェ
ノール性水酸基2個以上を有するノボラック型フェノー
ル樹脂が挙げられる。The phenol resin curing agent as the component (B) of the present invention may be any one generally known as a curing agent for epoxy resins, and examples thereof include phenol novolac resin and cresol novolac resin. A novolac type phenolic resin having two or more functional hydroxyl groups can be mentioned.
この(B)成分の配合量は、(A)成分100重量部に対
し、通常、30〜150重量部である。30重量部未満の場合
は、硬化が不充分であり、150重量部を超えると耐湿性
に劣る。好ましくは、50〜100重量部である。The blending amount of the component (B) is usually 30 to 150 parts by weight with respect to 100 parts by weight of the component (A). If it is less than 30 parts by weight, the curing will be insufficient, and if it exceeds 150 parts by weight, the moisture resistance will be poor. It is preferably 50 to 100 parts by weight.
本発明の(C)成分である硬化促進剤は、フェノール樹
脂を用いてエポキシ樹脂を硬化する際に、硬化促進剤と
して使用されることが知られているものであればいかな
るものであってもよい。この(C)成分の具体例として
は、2-メチルイミダゾール,2-エチル‐4-メチルイミダ
ゾール,1-シアノエチル‐2-エチル‐メチルイミダゾー
ル等のイミダゾール化合物;ベンジルジメチルアミン,
トリスジメチルアミノメチルフェノール等の第3アミン
化合物;トリフェニルホスフィン,トリシクロヘキシル
ホスフィン,トリブチルホスフィン,メチルジフェニル
ホスフィン等の有機ホスフィン化合物が挙げられ、これ
らは単独あるいは2種以上の混合系で使用される。The curing accelerator that is the component (C) of the present invention may be any one as long as it is known to be used as a curing accelerator when curing an epoxy resin with a phenol resin. Good. Specific examples of the component (C) include imidazole compounds such as 2-methylimidazole, 2-ethyl-4-methylimidazole, 1-cyanoethyl-2-ethyl-methylimidazole; benzyldimethylamine,
Examples include tertiary amine compounds such as trisdimethylaminomethylphenol; organic phosphine compounds such as triphenylphosphine, tricyclohexylphosphine, tributylphosphine, and methyldiphenylphosphine, and these are used alone or in a mixture of two or more kinds.
この(C)成分の配合量は(A)成分100重量部に対し
て、通常、0.01重量部〜10重量部である。0.01重量部未
満の場合には硬化性に劣り、10重量部を超えると耐湿性
が低下する。The blending amount of the component (C) is usually 0.01 to 10 parts by weight with respect to 100 parts by weight of the component (A). If it is less than 0.01 parts by weight, the curability is poor, and if it exceeds 10 parts by weight, the moisture resistance is lowered.
本発明の(D)成分である破砕状シリカ粉は、平均粒子
径が3〜100μmの範囲内のものであればいかなるもの
であってもよく、例えば、結晶性シリカ粉、溶融性シリ
カ粉、あるいはこれらの混合物が挙げられる。平均粒子
径が3μmの場合には、流動性が劣り、100μmを超え
ると成形時にゲートづまりを始めとする種々の作業上の
難点を生じるのみならず、樹脂封止型半導体素子の場合
には素子の誤動作の原因ともなり望ましくない。The crushed silica powder which is the component (D) of the present invention may be any one as long as it has an average particle size in the range of 3 to 100 μm, for example, crystalline silica powder, fusible silica powder, Alternatively, a mixture thereof may be used. When the average particle diameter is 3 μm, the fluidity is poor, and when it exceeds 100 μm, not only various work-related problems such as gate clogging during molding occur but also in the case of a resin-sealed semiconductor element, It may cause malfunction and is not desirable.
本発明の(E)成分である球状シリカ粉は、平均粒子径
が1〜50μmの範囲内のものであって、粒子の球状のも
のであればいかなるものであってもよく、例えば、結晶
性シリカ粉、溶融シリカ粉、あるいはこれらの混合物が
挙げられる。平均粒子径が上記範囲外である場合、成形
時における流動性の改善効果が少ない。The spherical silica powder which is the component (E) of the present invention has an average particle size in the range of 1 to 50 μm, and may be any as long as the particles have a spherical shape. Examples thereof include silica powder, fused silica powder, and a mixture thereof. When the average particle diameter is out of the above range, the effect of improving fluidity during molding is small.
さらに、本発明の(D)及び(E)成分が、最大粒径50
μm以下の(D)成分と平均粒子径5〜50μmの(E)
成分とからなり、(D)成分が(D)及び(E)成分の
合計量に対して10〜90容量%で配合される場合には、本
発明の組成物が極めて良好な成形性を示すとともに、得
られた硬化物が優れた耐熱衝撃性を有するものとなり好
ましい。また、本発明の(D)及び(E)成分が、平均
粒子径5〜100μmの(D)成分と平均粒子径1〜30μ
mの(E)成分とからなり、(E)成分が(D)及び
(E)成分の合計量に対して5〜60容量%で配合される
場合には、得られる硬化物が優れた耐熱衝撃性を有する
ものとなり好ましい。なお、この(D)成分と(E)成
分との粒径の比は、後者が1に対し、前者が3以上であ
ることが好ましい。この範囲を外れる場合には、流動性
の改善効果が十分に得られない。Further, the components (D) and (E) of the present invention have a maximum particle size of 50
(D) component of less than μm and (E) having an average particle size of 5 to 50 μm
When the component (D) is blended in an amount of 10 to 90% by volume based on the total amount of the components (D) and (E), the composition of the present invention exhibits extremely good moldability. At the same time, the obtained cured product has excellent thermal shock resistance, which is preferable. The components (D) and (E) of the present invention are composed of the component (D) having an average particle diameter of 5 to 100 μm and the average particle diameter of 1 to 30 μm.
When the (E) component is blended in an amount of 5 to 60% by volume based on the total amount of the (D) and (E) components, the resulting cured product has excellent heat resistance. It is preferable because it has impact resistance. The ratio of the particle diameters of the component (D) and the component (E) is preferably 1 for the latter and 3 or more for the former. If it is out of this range, the effect of improving the fluidity cannot be sufficiently obtained.
前記した(E)成分の配合量は(D)及び(E)成分の
合計量に対して、5〜90容量%である。この配合量が上
記した範囲を外れる場合には流動性の十分な改善効果が
得られない。また、前記した(D)及び(E)成分の合
計量は前記した(A),(B),(C),(D)及び
(E)成分の総配合量に対して、50〜75容量%である。
配合量が50容量%未満の場合には得られる硬化物が十分
な耐熱衝撃性を有することができず、75容量%を超える
と溶融粘度の上昇を招き成形性が低下する。The blending amount of the above-mentioned component (E) is 5 to 90% by volume based on the total amount of the components (D) and (E). If the blending amount is out of the above range, a sufficient effect of improving fluidity cannot be obtained. In addition, the total amount of the above-mentioned (D) and (E) components is 50 to 75 volumes with respect to the total compounding amount of the above-mentioned (A), (B), (C), (D) and (E) components. %.
If the content is less than 50% by volume, the cured product obtained cannot have sufficient thermal shock resistance, and if it exceeds 75% by volume, the melt viscosity increases and the moldability decreases.
本発明の(F)成分である界面処理剤は、エポキシシラ
ンと純水との混合物であり、本発明の効果を更に向上さ
せるための成分である。エポキシシランは一般式:YSi
(OR1)3(式中Yはエポキシ基を有する1価の有機
基、R1炭素数1〜5のアルキル基を表わす。)で示さ
れる化合物であり、例えば、γ‐グリシドキシプロピル
トリメトキシシランなどであり、純水とは、例えば蒸留
水、脱イオン水などの純水な水、特に無機もしくは有機
性イオンないしはイオン発生物質を含有しないか、それ
らの含有量がきわめて小さい水をいう。The interface treatment agent which is the component (F) of the present invention is a mixture of epoxysilane and pure water, and is a component for further improving the effect of the present invention. Epoxysilane has the general formula: YSi
(OR 1 ) 3 (wherein Y represents a monovalent organic group having an epoxy group, R 1 represents an alkyl group having 1 to 5 carbon atoms), and for example, γ-glycidoxypropyltri Methoxysilane and the like, and pure water refers to pure water such as distilled water and deionized water, especially water that does not contain inorganic or organic ions or ion-generating substances, or has a very small content thereof. .
本発明に用いられる界面処理剤は、上記エポキシシラン
と、純水を9:1〜9.95:0.05の割合で混合したものであ
る。この範囲外であると、耐湿性が劣る。The interface treatment agent used in the present invention is a mixture of the above-mentioned epoxysilane and pure water in a ratio of 9: 1 to 9.95: 0.05. If it is out of this range, the moisture resistance is poor.
本発明の組成物は、上記した各成分を加熱ロールによる
溶融混練、ニーダーによる溶融混練、押出機による溶融
混練、微粉砕等の特殊混合機による混合及びこれらの各
方法の適宜な組合せによって製造することができる。The composition of the present invention is produced by melt-kneading the above-mentioned components with a heating roll, melt-kneading with a kneader, melt-kneading with an extruder, mixing with a special mixer such as pulverization, and an appropriate combination of these methods. be able to.
なお、本発明の組成物は、必要に応じて高級脂肪酸、ワ
ックス類などの離型剤;アンチモン、リン化合物、臭素
や塩素を含む公知の難燃化剤が配合されてもよく、また
ポリスチレン、ポリメタクリル酸メチル、ポリ酢酸ビニ
ル、あるいはこれらの共重合体などの各種熱可塑性樹脂
やシリコーンオイル、シリコーンゴムなどを添加しても
よい。In addition, the composition of the present invention may be compounded with a releasing agent such as higher fatty acids and waxes; antimony, phosphorus compounds, known flame retardants containing bromine and chlorine, and polystyrene, if necessary. You may add various thermoplastic resins, such as polymethylmethacrylate, polyvinyl acetate, or these copolymers, silicone oil, silicone rubber, etc.
以下本発明の実施例を掲げ本発明を更に詳述する。な
お、表中の配合比は、特にことわらない限りは、すべて
重量%を表わす。Hereinafter, the present invention will be described in more detail with reference to Examples of the present invention. In addition, all the compounding ratios in the table represent% by weight unless otherwise specified.
[発明の実施例] 実施例1〜3 第1表に示す組成の各成分を使用し、本発明の組成物を
得た。上記組成物を、まず、ヘンシェルミキサー中で、
充填剤を界面処理剤で処理した後、残りの成分をミキサ
ー中に投入混合した後、60〜110℃の加熱ロールで混練
し、冷却後、粉砕して得られた。[Examples of the Invention] Examples 1 to 3 The components of the compositions shown in Table 1 were used to obtain compositions of the present invention. First, the above composition in a Henschel mixer,
After the filler was treated with the interfacial treatment agent, the remaining components were put into a mixer, mixed, kneaded with a heating roll at 60 to 110 ° C., cooled, and then pulverized.
なお、第1表中の各樹脂はオルトクレゾールノボラック
型エポキシ樹脂(エポキシ当量196、軟化点76℃)、難
燃性エポキシ樹脂(エポキシ当量270、軟化点30℃)、
フェノールノボラック樹脂(フェノール当量106、軟化
点97℃)を使用した。In addition, each resin in Table 1 is an ortho-cresol novolac type epoxy resin (epoxy equivalent 196, softening point 76 ° C), flame-retardant epoxy resin (epoxy equivalent 270, softening point 30 ° C),
Phenol novolac resin (phenol equivalent 106, softening point 97 ° C) was used.
比較例1〜6 第2表に示す組成の各成分を実施例と同様に処理し、比
較例とした。Comparative Examples 1 to 6 Each component having the composition shown in Table 2 was treated in the same manner as in the example to give a comparative example.
上記実施例1〜3及び比較例1〜6により得られた組成
分について下記の実験を行った。結果を第3表〜第5表
に示す。The following experiments were conducted on the composition components obtained in the above Examples 1 to 3 and Comparative Examples 1 to 6. The results are shown in Tables 3-5.
前記組成物の流動性を評価するため、高化式フローテス
ターを用いて173℃における溶融粘度を測定した。To evaluate the fluidity of the composition, the melt viscosity at 173 ° C. was measured using a Koka type flow tester.
さらに同組成物を用いて表面にPSG層を有する大型ペレ
ット評価用素子を低圧トランスファー成形により封止し
た。Further, using the same composition, a large-sized pellet evaluation element having a PSG layer on the surface was sealed by low-pressure transfer molding.
得られた試料素子について耐熱衝撃性を評価するため
に、熱衝撃試験(−65℃〜150℃の冷熱サイクルテス
ト)を行い、特性不良を測定した。In order to evaluate the thermal shock resistance of the obtained sample device, a thermal shock test (cooling cycle test at -65 ° C to 150 ° C) was performed to measure defective characteristics.
また、前記組成物を用いて低圧トランスファー成形法に
よりMOS型IC素子を樹脂封止し、得られた樹脂封止半導
体装置についてプレッシャークッカーテスト(2.5気圧
中でのテスト)を行ない、アルミ電極の腐食による耐湿
性を評価した。Further, a MOS type IC element is resin-sealed by a low-pressure transfer molding method using the above composition, and a pressure cooker test (test at 2.5 atmospheric pressure) is performed on the obtained resin-sealed semiconductor device to corrode the aluminum electrode. The moisture resistance was evaluated.
第3表〜第5表より明らかなとおり、実施例の本発明品
は比較品と比べて、耐熱衝撃性及び耐湿性において優れ
ており、又、溶融時における適度な粘度を有するもので
ある。As is clear from Tables 3 to 5, the inventive products of the examples are superior in thermal shock resistance and moisture resistance to the comparative products, and have an appropriate viscosity when melted.
[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、良好な成
形性を有するとともに、優れた耐熱衝撃性及び耐湿性を
有する硬化物を与えるため、半導体電子部品のパッケー
ジ材料として有用であり、その工業的価値は極めて大で
ある。 [Effects of the Invention] The epoxy resin composition for semiconductor encapsulation of the present invention is useful as a packaging material for semiconductor electronic components because it has a good moldability and gives a cured product having excellent thermal shock resistance and moisture resistance. And its industrial value is extremely large.
第1図は、実施例,比較例で使用したシリカ粉の粒度分
布曲線を示す図である。 A……破砕状溶融シリカ粉、平均粒径20μm B……破砕状溶融シリカ粉、平均粒径3μm (325meshパス、最大粒径44μm) C……球状溶融シリカ粉、平均粒径35μm D……球状溶融シリカ粉、平均粒径3μmFIG. 1 is a diagram showing a particle size distribution curve of silica powder used in Examples and Comparative Examples. A: crushed fused silica powder, average particle size 20 μm B: crushed fused silica powder, average particle size 3 μm (325 mesh pass, maximum particle size 44 μm) C …… spherical fused silica powder, average particle size 35 μm D …… Spherical fused silica powder, average particle size 3μm
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 H01L 23/31 (56)参考文献 特開 昭61−85432(JP,A) 特開 昭61−97322(JP,A) 特開 昭61−268750(JP,A)─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification number Internal reference number FI technical display location H01L 23/31 (56) References JP 61-85432 (JP, A) JP 61- 97322 (JP, A) JP-A-61-268750 (JP, A)
Claims (1)
粉; (E)平均粒子径1〜50μmを有する球状シリカ粉;及
び (F)エポキシシランと純水からなり、その重量比が9:
1〜9.95:0.05である界面処理剤を、(D)及び(E)成
分の合計量に対して0.1〜1.5重量% を含み、(E)成分の配合量が(D)及び(E)成分の
合計量に対して5〜90容量%であり、かつ(D)及び
(E)成分の合計量が(A),(B),(C),(D)
及び(E)の総配合量に対して50〜75容量%であること
を特徴とする半導体封止用エポキシ樹脂組成物。1. (A) Epoxy resin; (B) Phenolic resin curing agent; (C) Curing accelerator; (D) Crushed silica powder having an average particle diameter of 3 to 100 μm; (E) Average particle diameter of 1 to 1 Spherical silica powder having 50 μm; and (F) consisting of epoxysilane and pure water, the weight ratio of which is 9:
The surface treatment agent is 1 to 9.95: 0.05 in an amount of 0.1 to 1.5% by weight based on the total amount of the components (D) and (E), and the blending amount of the component (E) is the components (D) and (E). 5 to 90% by volume with respect to the total amount of (D) and (E) and the total amount of (A), (B), (C), (D)
And 50 to 75% by volume with respect to the total compounding amount of (E), an epoxy resin composition for semiconductor encapsulation.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60214622A JPH0651786B2 (en) | 1985-09-30 | 1985-09-30 | Epoxy resin composition for semiconductor device encapsulation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60214622A JPH0651786B2 (en) | 1985-09-30 | 1985-09-30 | Epoxy resin composition for semiconductor device encapsulation |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP28497093A Division JPH0744242B2 (en) | 1993-11-15 | 1993-11-15 | Epoxy resin composition for semiconductor device encapsulation |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6274924A JPS6274924A (en) | 1987-04-06 |
JPH0651786B2 true JPH0651786B2 (en) | 1994-07-06 |
Family
ID=16658776
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60214622A Expired - Lifetime JPH0651786B2 (en) | 1985-09-30 | 1985-09-30 | Epoxy resin composition for semiconductor device encapsulation |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0651786B2 (en) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2590908B2 (en) * | 1987-08-03 | 1997-03-19 | 松下電工株式会社 | Epoxy resin molding material |
JPS6462362A (en) * | 1987-09-03 | 1989-03-08 | Seitetsu Kagaku Co Ltd | Filler and polymer composition containing same |
JP2588922B2 (en) * | 1988-02-15 | 1997-03-12 | 日東電工株式会社 | Semiconductor device |
JPH01286346A (en) * | 1988-05-12 | 1989-11-17 | Nitto Denko Corp | Semiconductor device |
JPH0299551A (en) * | 1988-10-06 | 1990-04-11 | Toray Ind Inc | Epoxy-based resin composition |
JPH0672202B2 (en) * | 1988-10-06 | 1994-09-14 | 東レ株式会社 | Epoxy resin composition for semiconductor encapsulation |
JPH0791364B2 (en) * | 1988-10-06 | 1995-10-04 | 東レ株式会社 | Solder heat resistant epoxy resin composition for semiconductor encapsulation |
JPH0676539B2 (en) * | 1988-12-27 | 1994-09-28 | 東レ株式会社 | Epoxy-containing composition for semiconductor encapsulation |
JPH0645740B2 (en) * | 1989-03-01 | 1994-06-15 | 信越化学工業株式会社 | Epoxy resin composition for semiconductor encapsulation |
JPH0730236B2 (en) * | 1989-02-20 | 1995-04-05 | 東レ株式会社 | Epoxy resin composition for semiconductor encapsulation |
KR960012452B1 (en) * | 1989-02-20 | 1996-09-20 | 토레이 가부시키가이샤 | Semiconductor device-encapsulating epoxy resin composition |
KR950011902B1 (en) * | 1990-04-04 | 1995-10-12 | 도오레 가부시끼가이샤 | Epoxy resin composition for encapsulating semiconductor device |
JPH0733429B2 (en) * | 1990-04-04 | 1995-04-12 | 東レ株式会社 | Epoxy resin composition |
JPH04202555A (en) * | 1990-11-30 | 1992-07-23 | Toray Ind Inc | Epoxy resin composition for sealing semiconductor |
JPH062569B2 (en) * | 1990-12-31 | 1994-01-12 | 住友精化株式会社 | Silica fine powder |
JPH07242799A (en) * | 1994-09-19 | 1995-09-19 | Toray Ind Inc | Epoxy resin composition for semiconductor sealing |
DE69625627T2 (en) * | 1995-01-31 | 2003-09-11 | Sony Corp., Tokio/Tokyo | Detection circuit for a light signal |
JP2601255B2 (en) * | 1995-12-04 | 1997-04-16 | 電気化学工業株式会社 | Filler for semiconductor resin sealing |
KR100563352B1 (en) * | 1998-06-09 | 2006-03-22 | 닛토덴코 가부시키가이샤 | Semiconductor sealing epoxy resin composition and semiconductor device using the same |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6185432A (en) * | 1984-10-04 | 1986-05-01 | Hitachi Chem Co Ltd | Epoxy resin molding material for encapsulation of semiconductor device |
JPS6197322A (en) * | 1984-10-19 | 1986-05-15 | Denki Kagaku Kogyo Kk | Epoxy resin composition |
JPS61268750A (en) * | 1985-05-22 | 1986-11-28 | Shin Etsu Chem Co Ltd | Epoxy resin composition for semiconductor sealing use |
-
1985
- 1985-09-30 JP JP60214622A patent/JPH0651786B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPS6274924A (en) | 1987-04-06 |
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