JPH0710939B2 - Resin composition for electronic component encapsulation - Google Patents
Resin composition for electronic component encapsulationInfo
- Publication number
- JPH0710939B2 JPH0710939B2 JP60157716A JP15771685A JPH0710939B2 JP H0710939 B2 JPH0710939 B2 JP H0710939B2 JP 60157716 A JP60157716 A JP 60157716A JP 15771685 A JP15771685 A JP 15771685A JP H0710939 B2 JPH0710939 B2 JP H0710939B2
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- magnesium oxide
- resin
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- magnesium
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Description
【発明の詳細な説明】 「産業上の利用分野」 本発明は熱伝導体と耐金属摩耗性に優れる電子部品封止
用の樹脂組成物に関する。TECHNICAL FIELD The present invention relates to a resin composition for encapsulating electronic parts, which is excellent in heat conductor and metal abrasion resistance.
「従来の技術」 近年、半導体、抵抗体、コンデンサー、コイルなどの電
子部品を熱硬化性成型材料を用いて樹脂封止する方法が
盛んになっているが各種電子部品の信頼性に対する要求
はますます高まっており、それに伴って封止剤に対する
特性上の改良が強く望まれている。その一つに半導体の
集積化が進み、これに伴って発熱量も増大し、樹脂封止
された電子部品の熱放散性が大きな問題になっており、
これを満足させるためには熱伝導率の高い封止材の使用
が望まれている。"Conventional technology" In recent years, resin encapsulation of electronic parts such as semiconductors, resistors, capacitors, and coils using thermosetting molding materials has become popular, but there are demands for the reliability of various electronic parts. The property is increasing more and more, and accordingly, the improvement in properties of the encapsulant is strongly desired. One of them is the integration of semiconductors, and the amount of heat generated is also increasing, and the heat dissipation of resin-sealed electronic components has become a major issue.
In order to satisfy this, use of a sealing material having high thermal conductivity is desired.
従来の封止剤の多くは、経済性、耐熱性、耐湿性および
密着性の観点から、熱硬化性樹脂としてエポキシ樹脂を
使用し、これに無機質充填剤として熱伝導性や機械強度
をよくするためシリカ粉が加えられている。シリカ粉は
結晶性シリカまたは溶融シリカからなるものが殆どであ
る。Most conventional sealing agents use epoxy resin as a thermosetting resin from the viewpoint of economy, heat resistance, moisture resistance and adhesion, and improve thermal conductivity and mechanical strength as an inorganic filler. Therefore, silica powder is added. Most of silica powder is made of crystalline silica or fused silica.
しかしながら、これらのシリカ粉を用いた樹脂封止材料
は発熱量の大きい高集積化電子部品を封止するには熱伝
導率において未だ十分でなく、また、シリカ粉は硬度が
大きいため、これを用いた樹脂封止材料はトランスファ
ー成型や射出成型にあたって成型機や金型を摩耗させ長
期使用において未だ満足されておらず、更に優れた樹脂
封止材料が望まれている。However, the resin encapsulation materials using these silica powders are not yet sufficient in thermal conductivity for encapsulating highly integrated electronic components that generate a large amount of heat, and silica powders have high hardness, so The resin encapsulating material used is not yet satisfactory for long-term use due to abrasion of a molding machine or a mold during transfer molding or injection molding, and a further excellent resin encapsulating material is desired.
「発明が解決しようとする問題点」 そこで、上記の観点から鋭意検討した結果、無機質充填
材として単結晶酸化マグネシウム粉を使用したとき、熱
伝導率と耐金属摩耗性に好結果が得られることを見出
し、この発明を完成するに至った。"Problems to be solved by the invention" Therefore, as a result of intensive studies from the above viewpoint, when single crystal magnesium oxide powder was used as the inorganic filler, good results were obtained in thermal conductivity and metal wear resistance. And has completed the invention.
「問題点を解決するための手段」 すなわち、本発明はエポキシ樹脂に単結晶酸化マグネシ
ウムを混合してなる電子部品封止用樹脂組成物に係るも
のである。"Means for Solving Problems" That is, the present invention relates to a resin composition for electronic component encapsulation, which is obtained by mixing single crystal magnesium oxide with an epoxy resin.
以上、本発明を詳細に説明する。The present invention is described in detail above.
本発明に用いられる酸化マグネシウムは後記の方法によ
って得られる超高純度の単結晶酸化マグネシウムであ
る。Magnesium oxide used in the present invention is ultra-high purity single crystal magnesium oxide obtained by the method described below.
通常、酸化マグネシウムはマグネシウムの水酸化物、酢
酸塩、塩基性炭酸塩、シュウ酸塩などの熱分解によって
製造される。ところが、これらの塩分解により合成され
た酸化マグネシウムは二次凝集性が強く、二次粒子径が
大きいことが知られている。従って、樹脂と混練した場
合に分散性が十分でなく、熱伝導率も期待したほど高く
なり、純度も低いという欠点を有する。また、多結晶に
おいても同様の欠点が存する。Usually, magnesium oxide is produced by thermal decomposition of magnesium hydroxide, acetate, basic carbonate, oxalate or the like. However, it is known that the magnesium oxide synthesized by these salt decompositions has a strong secondary aggregation property and a large secondary particle size. Therefore, when it is kneaded with a resin, the dispersibility is not sufficient, the thermal conductivity is as high as expected, and the purity is low. In addition, there are similar defects in polycrystals.
本発明に用いられる高純度の単結晶酸化マグネシウム粉
は下記の特色を備えている: (a) 平均粒子径0.01〜20μmの範囲にある、 (b) 純度は99.9%以上である、 (c) 塩素イオン及び臭素イオンの含有量は何れも5p
pm以下であり、その他の不純物も極めて少量しか含有し
ない、 (d) その硬度においてシリカよりも低い。The high-purity single-crystal magnesium oxide powder used in the present invention has the following features: (a) average particle size is in the range of 0.01 to 20 μm, (b) purity is 99.9% or more, (c) The content of chlorine ion and bromine ion is 5p
pm or less and also contains a very small amount of other impurities. (d) Its hardness is lower than that of silica.
(e) 樹脂に配合した組成物は5×1013Ω・cm以上と
いう高い体積固有抵抗率を備えている、 (f) 樹脂と混練した場合に優れた分散性を発揮す
る。この優れた分散性は得られる成形品の高いシャルピ
ー衝撃強度に具現される、 本発明に用いられる上記の高純度の単結晶酸化マグネシ
ウム粉は下記の方法によって得られるものである: マグネシウム蒸発部においてマグネシウムを不活性ガス
雰囲気下で700℃以上の温度に加熱して発生させた純度9
9.9%以上のマグネシウム蒸気と酸素含有気体とを併流
で互いに接触させながら、下記の各条件が充足される様
に反応させる: マグネシウム蒸気分圧が1気圧未満、 酸素含有気体の酸素分圧がマグネシウム蒸気分圧の1/
2以上、 反応温度が800〜2000℃。(E) The composition blended with the resin has a high volume resistivity of 5 × 10 13 Ω · cm or more, and (f) exhibits excellent dispersibility when kneaded with the resin. This excellent dispersibility is realized in the high Charpy impact strength of the obtained molded product. The above-mentioned high-purity single crystal magnesium oxide powder used in the present invention is obtained by the following method: Purity generated by heating magnesium to a temperature of 700 ℃ or higher in an inert gas atmosphere 9
9.9% or more of magnesium vapor and oxygen-containing gas are contacted in parallel with each other, and the reaction is performed so that the following conditions are satisfied: Magnesium vapor partial pressure is less than 1 atm, oxygen partial pressure of oxygen-containing gas is magnesium 1 / steam partial pressure
2 or more, reaction temperature is 800 ~ 2000 ℃.
この発明においては、樹脂への分散性に優れた単結晶酸
化マグネシウムを充填剤に用いることにより、熱伝導率
が高い封止材料が得られ電子部品の熱放散性を満足させ
ることができ、しかも金属摩耗が少なく成型機や金型の
長期間使用を可能とすることができる。In the present invention, by using a single crystal magnesium oxide having excellent dispersibility in a resin as a filler, a sealing material having high thermal conductivity can be obtained, and heat dissipation of electronic parts can be satisfied, and It is possible to use a molding machine or a mold for a long period of time with less metal wear.
この発明の電子部品封止用樹脂組成物は、単結晶酸化マ
グネシウムをエポキシ樹脂に配合し、これに硬化剤や各
種添加剤を加え、これらの配合組成物を通常の混合およ
び混練手段、たとえば釜による溶融混練、ロールによる
溶融混練、押出機による溶融混練などの方法で均一に混
合または混練することにより調製される。The electronic component sealing resin composition of the present invention is obtained by blending single crystal magnesium oxide with an epoxy resin, adding a curing agent and various additives thereto, and mixing the blended composition with usual mixing and kneading means such as a pot. It is prepared by uniformly mixing or kneading by a method such as melt kneading according to, melt kneading with a roll, melt kneading with an extruder, or the like.
単結晶酸化マグネシウムの使用割合は、酸化マグネシウ
ムを多くすればするほど熱伝導率は大きくなるが、反
面、組成物の流動性が低下し、余りに多すぎると、電子
部品を完全に封止できなくなって未充填やボイドが多発
し耐湿性の低下を招く恐れがある。また、圧力をかけて
樹脂を注入する場合、電子部品の強度の弱い部分、たと
えば半導体素子とリード部とを結ぶボンディングワイヤ
ーなどを切断する危険性がある。一方、酸化マグネシウ
ムが余りに少なくなってしまうと硬化が小さくてこの発
明の目的を達成できなくなる。従って、好ましくは全組
成物中10〜85重量%である。The proportion of single-crystal magnesium oxide used increases as the amount of magnesium oxide increases, but on the other hand, the fluidity of the composition decreases, and if it is too large, the electronic component cannot be completely sealed. As a result, unfilling and voids frequently occur, which may lead to deterioration in moisture resistance. Further, when pressure is applied to inject the resin, there is a risk of cutting a weak portion of the electronic component, such as a bonding wire connecting the semiconductor element and the lead portion. On the other hand, if the amount of magnesium oxide is too small, the hardening is so small that the object of the present invention cannot be achieved. Therefore, it is preferably 10 to 85% by weight in the total composition.
この発明においては、充填剤として単結晶酸化マグネシ
ウム単独で用い得る他に、単結晶酸化マグネシウムとそ
れ以外の無機質充填剤、たとえば、結晶性シリカや溶融
シリカなどのシリカ、アルミナ、炭酸カルシウム、タル
クなどを併用することもできるが、これらの無機質充填
剤の使用量は単結晶酸化マグネシウムと併せて全組成物
中の15〜85重量%が望ましい。無機質充填剤15重量%未
満では熱膨張率や機械強度の面で欠点が目立ち好ましく
ない。In the present invention, single crystal magnesium oxide alone can be used as the filler, and single crystal magnesium oxide and other inorganic fillers, for example, silica such as crystalline silica or fused silica, alumina, calcium carbonate, talc, etc. However, the amount of these inorganic fillers used is preferably 15 to 85% by weight based on the total composition, together with the single crystal magnesium oxide. If the inorganic filler is less than 15% by weight, defects are conspicuous and not preferable in terms of thermal expansion coefficient and mechanical strength.
この発明に用いられるエポキシ樹脂としては、例えばク
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、臭素化フェノールノボラック型エポキシ樹脂及び脂
環型エポキシ樹脂等を挙げることができる。また、この
樹脂の硬化剤としてはジアミノジフェニルメタン、ジア
ミノジフェニルスルホン、メタフェニレンジアミンなど
のアミン系硬化剤、無水フタル酸、無水ピロメリット
酸、無水マレイン酸などの酸無水物系硬化剤、またはフ
ェノールノボラック樹脂、クレゾールノボラック樹脂な
どのノボラック系硬化剤などのいずれも公知の硬化剤を
使うことができる。これにはイミダゾールやその誘導
体、3級アミンの誘導体、ホスフィン系誘導体などの硬
化促進剤を添加してもよく、またこれ以外の添加剤とし
て、離型剤、カップリング剤、難燃剤などが必要に応じ
て用いられる。Examples of the epoxy resin used in the present invention include cresol novolac type epoxy resin, phenol novolac type epoxy resin, bisphenol A type epoxy resin, brominated phenol novolac type epoxy resin and alicyclic epoxy resin. Further, as a curing agent for this resin, an amine-based curing agent such as diaminodiphenylmethane, diaminodiphenylsulfone, or metaphenylenediamine, an acid anhydride-based curing agent such as phthalic anhydride, pyromellitic dianhydride, maleic anhydride, or phenol novolac. Known curing agents can be used for the resin and novolac-based curing agents such as cresol novolac resin. A curing accelerator such as imidazole or its derivative, a tertiary amine derivative, or a phosphine derivative may be added to this, and a release agent, a coupling agent, a flame retardant, etc. are required as other additives. Used according to.
以上の様に、この発明の電子部品封止用樹脂組成物は下
記の長所を備えている: (イ) 成形時に成形機及び金型を僅かしか損耗しな
い、 (ロ) 熱伝導率大、即ち熱放散性大の樹脂封止電子部
品を製造可能、 (ニ) 成形品のシャルピー衝撃強度大、 (ホ) 体積固有抵抗率(150℃)大。As described above, the resin composition for encapsulating electronic parts of the present invention has the following advantages: (a) The molding machine and the mold are slightly worn at the time of molding, and (b) the thermal conductivity is large, that is, We can manufacture resin-sealed electronic parts with high heat dissipation, (d) Large Charpy impact strength of molded products, and (e) Large volume resistivity (150 ° C).
従って、上記組成物は工業的に極めて有用な封止材を提
供する素材である。Therefore, the above composition is a material that provides a very useful sealing material industrially.
上記した本発明の樹脂組成物は、配合後適宜の形状に成
形されるが、これによる電子部品の封止は従来公知の注
形成形、圧縮成形、トランスファー成形、射出成形のい
ずれでも行うことができる。The above-described resin composition of the present invention is molded into an appropriate shape after blending, and the sealing of electronic parts by this can be performed by any of conventionally known casting molding, compression molding, transfer molding, and injection molding. it can.
「実施例」 以下、実施例に従って具体的に説明するが、本発明はこ
れらに限定されるものではない。"Examples" Hereinafter, specific examples will be described, but the present invention is not limited thereto.
参考例 (単結晶酸化マグネシウムの製造) 酸化反応器に900℃に加熱気化させた純度99.9%のマグ
ネシウムと、希釋剤として純度99.9%のアルゴンガスを
導入してマグネシウム蒸気圧0.04気圧とし、次に純度9
9.9%の酸素ガスを導入しながら温度1000℃で酸化させ
て、粒子径が主に0.01〜20μmからなる純度99.9%の単
結晶酸化マグネシウムを得た。Reference Example (Production of Single Crystal Magnesium Oxide) Magnesium having a purity of 99.9% heated and vaporized to 900 ° C. and argon gas having a purity of 99.9% as a diluting agent were introduced into an oxidation reactor so that the magnesium vapor pressure was 0.04 atm. To purity 9
Oxidation was carried out at a temperature of 1000 ° C. while introducing 9.9% oxygen gas to obtain single-crystal magnesium oxide having a particle size of 0.01 to 20 μm and a purity of 99.9%.
実施例1 オルソクレゾールノボラックエポキシ樹脂(エポキシ当
量214,軟化点84℃)198重量部、臭素化フェノールノボ
ラックエポキシ樹脂(エポキシ当量275,軟化点84℃)22
重量部、フェノール樹脂(軟化点80℃)110重量部、三
酸化アンチモン33重量部、参考例で得た単結晶酸化マグ
ネシウム826重量部、2−エチル−4−メチルイミダゾ
ール4重量部、カルナバワックス4重量部、シランカッ
プリング剤(日本ユニカ社製A−187)4重量部を配合
し、二本ロールで80〜100℃で溶融混練したのち、粉砕
して電子部品封止用樹脂組成物を得た。Example 1 198 parts by weight of orthocresol novolac epoxy resin (epoxy equivalent 214, softening point 84 ° C.), brominated phenol novolac epoxy resin (epoxy equivalent 275, softening point 84 ° C.) 22
Parts by weight, phenol resin (softening point 80 ° C.) 110 parts by weight, antimony trioxide 33 parts by weight, single crystal magnesium oxide 826 parts by weight obtained in the reference example, 2-ethyl-4-methylimidazole 4 parts by weight, carnauba wax 4 Parts by weight, and 4 parts by weight of a silane coupling agent (A-187 manufactured by Nippon Unica Co., Ltd.) are mixed and melt-kneaded with a two-roll at 80 to 100 ° C., followed by pulverization to obtain a resin composition for sealing electronic parts. It was
実施例2 実施例1における単結晶酸化マグネシウム826重量部に
代えて、同じ単結晶酸化マグネシウム413重量部と溶融
シリカ(竜森社製RD−8)413重量部を使用して成形材
料をた。Example 2 Instead of 826 parts by weight of single crystal magnesium oxide in Example 1, 413 parts by weight of the same single crystal magnesium oxide and 413 parts by weight of fused silica (RD-8 manufactured by Tatsumori Co., Ltd.) were used to prepare a molding material.
比較例1 実施例1における単結晶酸化マグネシウム826重量部に
代えて、溶融シリカ(実施例2と同一品)826重量部を
使用して成形材料を調製した。Comparative Example 1 A molding material was prepared by using 826 parts by weight of fused silica (the same product as in Example 2) instead of 826 parts by weight of the single crystal magnesium oxide in Example 1.
(電子部品封止用樹脂組成物の特性評価) 実施例1,2および比較例の樹脂組成物をトランスファー
成形して、成形品の特性評価を行ない結果を第1表に示
した。比較例に比べて実施例1と2は金属と擦り合わせ
た場合の金属摩損が少なく、また成形品の熱伝導率が大
きいという特異性を示し、電気的特性および機械的特性
は特に問題がないことが確認された。(Characteristic Evaluation of Resin Composition for Encapsulating Electronic Parts) The resin compositions of Examples 1 and 2 and Comparative Example were transfer molded, and the characteristics of the molded products were evaluated. The results are shown in Table 1. Compared with the comparative example, the examples 1 and 2 show the peculiarity that the metal wear is small when they are rubbed with the metal, and the thermal conductivity of the molded product is large, and there is no particular problem with respect to electrical properties and mechanical properties. It was confirmed.
実施例3 オクソクレゾールノボラックエポキシ樹脂(エポキシ当
量214、軟化点84℃)198重量部、臭素代フェノールノボ
ラックエポキシ樹脂(エポキシ当量278、軟化点84℃)2
2重量部、フェノール樹脂(軟化点80℃)110重量部、三
酸化アンチモン33重量部、単結晶酸化マグネシウム826
重量部、2-エチル4-メチルイミダゾール4重量部、カル
ナバワックス4重量部及びシランカップリング剤[商品
名:A-187(二本ユニカ社製)]4重量部を配合し、二本
ロールで80〜100℃において溶融混練した後、粉砕して
電子部品封止用樹脂組成物を得た。この組成物をトラン
スファー成形して得られた成形品の熱伝導率、引張強
度、シャルピー衝撃強度及び体積固有抵抗率(150℃)
を測定した結果を第2表に示す。 Example 3 Oxocresol novolac epoxy resin (epoxy equivalent 214, softening point 84 ° C.) 198 parts by weight, bromine phenol novolac epoxy resin (epoxy equivalent 278, softening point 84 ° C.) 2
2 parts by weight, phenol resin (softening point 80 ° C) 110 parts by weight, antimony trioxide 33 parts by weight, single crystal magnesium oxide 826
2 parts by weight, 4 parts by weight of 2-ethyl 4-methylimidazole, 4 parts by weight of carnauba wax and 4 parts by weight of a silane coupling agent [trade name: A-187 (manufactured by Nihon Unica Co., Ltd.)] are mixed in a double roll. After melt-kneading at 80 to 100 ° C., it was pulverized to obtain a resin composition for sealing electronic parts. The thermal conductivity, tensile strength, Charpy impact strength and volume resistivity (150 ° C) of the molded product obtained by transfer molding of this composition
Table 2 shows the results of the measurement.
比較例2 本願実施例1で用いた単結晶酸化マグネシウム826重量
部に代えて、酸化マグネシウム(3200℃で溶融して調
製)826重量部を用いて同様に樹脂組成物を作成し、成
形品の熱伝導率、引張強度、シャルピー衝撃強度及び体
積固有抵抗率(150℃)を測定した結果を第2表に示
す。Comparative Example 2 A resin composition was prepared in the same manner by using 826 parts by weight of magnesium oxide (prepared by melting at 3200 ° C.) instead of 826 parts by weight of the single crystal magnesium oxide used in Example 1 of the present application. Table 2 shows the results of measurement of thermal conductivity, tensile strength, Charpy impact strength and volume resistivity (150 ° C).
比較例3 本願実施例1で用いた単結晶酸化マグネシウム826重量
部に代えて、酸化マグネシウム(2100℃で焼成して調
製)826重量部を用いて、同様に樹脂組成物を作成し、
成形品の熱伝導率、引張強度、シャルピー衝撃強度及び
体積固有抵抗率(150℃)を測定した結果を第2表に示
す。Comparative Example 3 A resin composition was similarly prepared using 826 parts by weight of magnesium oxide (prepared by baking at 2100 ° C.) instead of 826 parts by weight of the single crystal magnesium oxide used in Example 1 of the present application,
Table 2 shows the results of measuring the thermal conductivity, tensile strength, Charpy impact strength, and volume resistivity (150 ° C) of the molded product.
比較例4 本願実施例1で用いた単結晶酸化マグネシウム826重量
部に代えて、酸化マグネシウム(1200℃で焼成して調
製)826重量部を用いて、同様に樹脂組成物を作成し、
成形品の熱伝導率、引張強度、シャルピー衝撃強度及び
体積固有抵抗率(150℃)を測定した結果を第2表に示
す。Comparative Example 4 A resin composition was similarly prepared using 826 parts by weight of magnesium oxide (prepared by firing at 1200 ° C.) instead of 826 parts by weight of the single crystal magnesium oxide used in Example 1 of the present application,
Table 2 shows the results of measuring the thermal conductivity, tensile strength, Charpy impact strength, and volume resistivity (150 ° C) of the molded product.
「発明の効果」 以上から明らか如く、本発明によれば酸化マグネシウム
を単結晶のかたちで配合することにより、熱硬化性樹脂
への分散性が優れ、その結果酸化マグネシウムの熱伝導
率に優れる特性を活かして電子部品封止用樹脂組成物と
して従来にない優れた熱放散性を有し、且つ金属摩耗性
が少ない成形作業性に優れたものを提供することが可能
となった。 "Effects of the Invention" As is apparent from the above, according to the present invention, by mixing magnesium oxide in the form of a single crystal, the dispersibility in a thermosetting resin is excellent, and as a result, the magnesium oxide has excellent thermal conductivity. By utilizing the above, it has become possible to provide a resin composition for encapsulating electronic parts, which has an unprecedentedly excellent heat dissipation property and is excellent in molding workability with less metal abrasion.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 吉田 孝三郎 山口県宇部市大字小串1978番地の5 宇部 興産株式会社宇部研究所内 (56)参考文献 特開 昭49−66761(JP,A) 特開 昭62−115757(JP,A) 特開 昭61−85474(JP,A) 特開 昭61−101524(JP,A) ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Kozaburo Yoshida 5 1978, Ogushi, Ube City, Yamaguchi Prefecture, Ube Laboratory, Ube Institute of Industrial Manufacturing (56) Reference JP-A-49-66761 (JP, A) JP-A-SHO 62-115757 (JP, A) JP-A-61-85474 (JP, A) JP-A-61-101524 (JP, A)
Claims (2)
結晶酸化マグネシウムを10〜85重量%含有し、その体積
固有抵抗率が5×1013Ω・cm以上である電子部品封止用
樹脂組成物: 平均粒子径0.01〜20μm、 純度≧99.9%、 塩素イオン含有量≦5ppm及び臭素イオン含有量≦5pp
m。1. A resin for encapsulating an electronic component, which comprises an epoxy resin containing 10 to 85% by weight of single crystal magnesium oxide satisfying the following requirements and having a volume resistivity of 5 × 10 13 Ω · cm or more. Composition: average particle size 0.01 to 20 μm, purity ≧ 99.9%, chloride ion content ≦ 5 ppm and bromine ion content ≦ 5 pp
m.
れた単結晶酸化マグネシウムを含有し、その体積固有抵
抗率が5×1013Ω・cm以上である請求項1に記載の電子
部品封止用樹脂組成物: マグネシウム蒸発部においてマグネシウムを不活性ガス
雰囲気下で700℃以上の温度に加熱して発生させた純度9
9.9%以上のマグネシウム蒸気と酸素含有気体とを併流
で互いに接触させながら、下記の各条件が充足される様
に反応させる: マグネシウム蒸気分圧が1気圧未満、 酸素含有気体の酸素分圧がマグネシウム蒸気分圧の1/
2以上、 反応温度が800〜2000℃。2. The electronic component encapsulation according to claim 1, wherein the epoxy resin contains single crystal magnesium oxide produced by the following method, and its volume resistivity is 5 × 10 13 Ω · cm or more. Resin composition: Purity generated by heating magnesium to a temperature of 700 ° C. or higher in an inert gas atmosphere in a magnesium evaporator 9
9.9% or more of magnesium vapor and oxygen-containing gas are contacted in parallel with each other, and the reaction is performed so that the following conditions are satisfied: Magnesium vapor partial pressure is less than 1 atm, oxygen partial pressure of oxygen-containing gas is magnesium 1 / steam partial pressure
2 or more, reaction temperature is 800 ~ 2000 ℃.
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60157716A JPH0710939B2 (en) | 1985-07-17 | 1985-07-17 | Resin composition for electronic component encapsulation |
| US06/885,083 US4677026A (en) | 1985-07-17 | 1986-07-14 | Resin composition for sealing electronic parts, and hydration-resistant magnesia powder and process for preparation thereof |
| EP86109760A EP0209847A3 (en) | 1985-07-17 | 1986-07-16 | Resin composition for sealing electronic parts, and hydration-resistant magnesia powder and process for preparation thereof |
| EP19910117811 EP0476709A3 (en) | 1985-07-17 | 1986-07-16 | Hydration-resistant magnesia powder and process for preparation thereof |
| US07/034,439 US4766162A (en) | 1985-07-17 | 1987-04-03 | Resin composition for sealing electronic parts, and hydration-resistant magnesia powder and process for preparation thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60157716A JPH0710939B2 (en) | 1985-07-17 | 1985-07-17 | Resin composition for electronic component encapsulation |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6218441A JPS6218441A (en) | 1987-01-27 |
| JPH0710939B2 true JPH0710939B2 (en) | 1995-02-08 |
Family
ID=15655811
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60157716A Expired - Lifetime JPH0710939B2 (en) | 1985-07-17 | 1985-07-17 | Resin composition for electronic component encapsulation |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0710939B2 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010163598A (en) * | 2008-12-18 | 2010-07-29 | Panasonic Corp | Prepreg, method for producing the same, and printed wiring board using the same |
| JP5507477B2 (en) * | 2011-01-20 | 2014-05-28 | パナソニック株式会社 | Epoxy resin composition for semiconductor encapsulation and semiconductor device |
| JP5795168B2 (en) * | 2011-02-07 | 2015-10-14 | 明和化成株式会社 | Thermally conductive resin composition and semiconductor package |
| US9856146B2 (en) | 2013-05-24 | 2018-01-02 | Sakai Chemical Industry Co., Ltd. | Magnesium oxide particles, magnesium oxide particle production method, resin composition and molded body using such resin composition, and adhesive or grease |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS568061B2 (en) * | 1972-11-06 | 1981-02-21 | ||
| JPS6185474A (en) * | 1984-10-03 | 1986-05-01 | Daicel Chem Ind Ltd | Heat-conductive resin composition |
| JPS61101524A (en) * | 1984-10-25 | 1986-05-20 | Toshiba Chem Corp | Sealing resin composition |
| JPS62115757A (en) * | 1985-07-17 | 1987-05-27 | Ube Ind Ltd | Resin composition for encapsulating electronic components |
-
1985
- 1985-07-17 JP JP60157716A patent/JPH0710939B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6218441A (en) | 1987-01-27 |
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