JPH01185321A - Epoxy resin molding material - Google Patents
Epoxy resin molding materialInfo
- Publication number
- JPH01185321A JPH01185321A JP800788A JP800788A JPH01185321A JP H01185321 A JPH01185321 A JP H01185321A JP 800788 A JP800788 A JP 800788A JP 800788 A JP800788 A JP 800788A JP H01185321 A JPH01185321 A JP H01185321A
- Authority
- JP
- Japan
- Prior art keywords
- epoxy resin
- agent
- molding material
- resin molding
- microns
- 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
Links
- 239000003822 epoxy resin Substances 0.000 title claims abstract description 25
- 229920000647 polyepoxide Polymers 0.000 title claims abstract description 25
- 239000012778 molding material Substances 0.000 title claims description 14
- 239000000835 fiber Substances 0.000 claims abstract description 12
- 239000000919 ceramic Substances 0.000 claims abstract description 8
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 7
- 239000003431 cross linking reagent Substances 0.000 claims abstract description 5
- 239000000945 filler Substances 0.000 claims abstract description 5
- 239000006087 Silane Coupling Agent Substances 0.000 claims abstract description 4
- 239000003086 colorant Substances 0.000 claims abstract description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 10
- 239000000377 silicon dioxide Substances 0.000 claims description 5
- 239000007822 coupling agent Substances 0.000 claims description 4
- 239000006082 mold release agent Substances 0.000 claims description 3
- 239000000654 additive Substances 0.000 claims description 2
- 238000004381 surface treatment Methods 0.000 claims 1
- 239000000463 material Substances 0.000 abstract description 4
- 125000003700 epoxy group Chemical group 0.000 abstract description 2
- 230000000694 effects Effects 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 238000007789 sealing Methods 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 230000006355 external stress Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000011256 inorganic filler Substances 0.000 description 2
- 229910003475 inorganic filler Inorganic materials 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 238000005476 soldering Methods 0.000 description 2
- 238000001721 transfer moulding Methods 0.000 description 2
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000004984 aromatic diamines Chemical class 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 239000008393 encapsulating agent Substances 0.000 description 1
- 239000012765 fibrous filler Substances 0.000 description 1
- -1 glycidyl ester Chemical class 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 239000003566 sealing material Substances 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Polyesters Or Polycarbonates (AREA)
- Epoxy Resins (AREA)
- Sealing Material Composition (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は電気部品や電子部品を封止する樹脂モールド品
に主として用いられるエポキシ樹脂成形材料に関するも
のである。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to an epoxy resin molding material mainly used for resin molded products for sealing electrical and electronic components.
近年、電気、電子機器の高性能化、高信頼性、生産性向
上のため、プラスチックによる封止がなされるようにな
ってきた。これらの封止用成形材料としてはエポキシ樹
脂にシリカ等の粉末状無機質充填剤を含有させたものが
一般に用いられている。In recent years, in order to improve the performance, reliability, and productivity of electric and electronic equipment, plastic sealing has been used. As these molding materials for sealing, epoxy resins containing powdered inorganic fillers such as silica are generally used.
最近のデバイスのパッケージ形態は、従来のDIP型か
ら高密度実装をするためにSOP、QFP等の表面実装
対応パッケージの比率が増加している。表面実装対応で
問題になってくるのは、パッケージ全体が直接に半田等
の高熱に暴露されることで、このような熱シヨツク後の
耐湿性低下が大きな問題になってくる。更に表面実装対
応パッケージは従来パッケージよシ肉厚が薄く、リード
間のビンピッチも従来の100ミルから50〜75ミル
と狭くなってきており機械強度が低下しているので、組
立加工時の外力応力により密着性(ベレットと封止材、
リードと封止材の界面)が低下するため耐湿性が低下す
るという問題も発生している。In recent device packaging formats, the proportion of surface-mountable packages such as SOP and QFP is increasing from the conventional DIP type to enable high-density mounting. The problem with surface mounting is that the entire package is directly exposed to the high heat of soldering, etc., and the drop in moisture resistance after such heat shock becomes a major problem. Furthermore, surface mount compatible packages have thinner walls than conventional packages, and the pitch between the leads has narrowed from the conventional 100 mils to 50-75 mils, reducing mechanical strength and reducing external stress during assembly. Adhesion (belt and sealing material,
Another problem has arisen in that moisture resistance is reduced due to a decrease in the interface between the lead and the encapsulant.
本発明は従来の技術における上述の問題点に鑑みてなさ
れたもので、その目的とするところは、後加工時に発生
する外的応力を低減すると共に、密着性を向上し、耐湿
性の優れたエポキシ樹脂成形材料を提供することにある
。The present invention was made in view of the above-mentioned problems in the conventional technology, and its purpose is to reduce the external stress generated during post-processing, improve adhesion, and provide a material with excellent moisture resistance. Our objective is to provide epoxy resin molding materials.
C問題点を解決するための手段〕
本発明はエポキシ樹脂に対し、必要に応じて架橋剤、硬
化剤、硬化促進剤、離型剤、着色剤、カップリング剤、
充填剤等の添加剤を添加してなるエポキシ樹脂成形材料
において、直径1〜10ミクロン、長さ10〜150ミ
クロンのセラミックファイバーの表面をシラン系カップ
リング剤で表面処理してから含有したことを特徴とする
エポキシ樹脂成形材料のため上記目的を達成することが
できたもので、以下本発明の詳細な説明する。Means for Solving Problem C] The present invention provides an epoxy resin with a crosslinking agent, a curing agent, a curing accelerator, a mold release agent, a coloring agent, a coupling agent,
In epoxy resin molding materials containing additives such as fillers, the surface of ceramic fibers with a diameter of 1 to 10 microns and a length of 10 to 150 microns is treated with a silane coupling agent. The above object has been achieved because of the characteristic epoxy resin molding material, and the present invention will be described in detail below.
本発明に用いるエポキシ樹脂としては1分子中に2個以
上のエポキシ基を有する硬化可能なエポキシ樹脂である
ならばビスフェノールA型エポキシ樹脂、ノポヲック型
エポキシ樹脂、可撓性エポキシ樹脂、ハロゲン化エポキ
シ樹脂、グリシジルエステル型エポキシ樹脂、高分子型
エポキシ樹脂各れでもよく特に限定するものではない。The epoxy resin used in the present invention is a curable epoxy resin having two or more epoxy groups in one molecule, such as bisphenol A type epoxy resin, Nopowoc type epoxy resin, flexible epoxy resin, and halogenated epoxy resin. , a glycidyl ester type epoxy resin, or a polymer type epoxy resin, without any particular limitation.
架橋剤としてはフェノール樹脂、メラミン樹脂、アクリ
ル樹脂、ユリア樹脂、イソシアネート等が用いられ、特
に限定するものではない。硬化剤としては脂肪族ポリア
ミン、ポリアミド樹脂、芳香族ジアミン等のアミン系硬
化剤、酸無水物硬化剤、ルイス酸錯化合物等が用いられ
、特に限定するものではない。硬化促進剤としてはリン
系及び又は3級アミン系硬化促進剤を用いることが必要
である。As the crosslinking agent, phenol resin, melamine resin, acrylic resin, urea resin, isocyanate, etc. are used, and there are no particular limitations. As the curing agent, amine curing agents such as aliphatic polyamines, polyamide resins, aromatic diamines, acid anhydride curing agents, Lewis acid complex compounds, etc. can be used, and there are no particular limitations. As the curing accelerator, it is necessary to use a phosphorus-based and/or tertiary amine-based curing accelerator.
充填剤としてはセフミックファイバーを含有させること
が必要であるが、更に必要に応じて他のガラスN&維、
アスベストR維、パルプ繊維等の繊維質充填剤やシリカ
、三酸化アンチモン、炭酸カルシウム、りV−、タルク
、ガラス粉、水e化アルミニウム等の無機質充填剤を併
用してもよい。セラミックブアイパーとしては、直径が
1〜10ミクロン、長さが10〜150ミクロンである
ことが必要である。即ち直径が1ミクロン未満、長さが
10ミクロン未満では機械的強度が向上し難く、直径が
10ミクロン、長さが150ミクロンをこえると充填性
、成形性が低下する傾向にあるからである。又セフミッ
クファイバーの表面をシラン系カップリング剤で表面す
ることがより分散性を向上させる点でよく必要である。It is necessary to contain cefmic fiber as a filler, but if necessary, other glass N & fibers,
Fibrous fillers such as asbestos R fibers and pulp fibers and inorganic fillers such as silica, antimony trioxide, calcium carbonate, silica, talc, glass powder, and aluminum hydrate may be used in combination. The ceramic eyeper needs to have a diameter of 1 to 10 microns and a length of 10 to 150 microns. That is, if the diameter is less than 1 micron and the length is less than 10 microns, it is difficult to improve mechanical strength, and if the diameter exceeds 10 microns and the length is more than 150 microns, filling properties and moldability tend to decrease. Furthermore, it is often necessary to coat the surface of the cefmic fiber with a silane coupling agent in order to further improve dispersibility.
更にセラミックファイバーの量はシリカ100重量部c
以下単に部と記す)に対して5〜(資)部であることが
好ましい。即ち5部未満では機械的強度が向上せず、関
部をこえると充填性、成形性が低下する傾向にあるから
である。Furthermore, the amount of ceramic fiber is 100 parts by weight of silica.
The amount is preferably 5 to (equity) parts. That is, if the amount is less than 5 parts, the mechanical strength will not improve, and if it exceeds the critical point, the filling properties and moldability will tend to decrease.
離型剤、着色剤、カップリング剤更にはトリフェ二/+
/ホスフィン等については通常用いられているものをそ
のまま用いることができるので特に限定するものではな
い。かくして上記材料を混合、混練、粉砕し更に必要に
応じて造粒して成形材料を得るものである。更に該成形
材料の成形については、トランスファー成形、射出成形
等によるトランジスター、ダイオード、コンデンサー、
フィルター、整流器、抵抗体、コイル等の電子部品の多
数個数シ成形に適することは勿論、圧縮成形等にも適用
できるものである。Mold release agent, coloring agent, coupling agent and even triphenyl/+
/Phosphine and the like are not particularly limited, as commonly used ones can be used as they are. In this way, the above materials are mixed, kneaded, pulverized, and further granulated if necessary to obtain a molding material. Furthermore, regarding the molding of the molding material, transistors, diodes, capacitors, etc. by transfer molding, injection molding, etc.
It is suitable not only for molding large numbers of electronic components such as filters, rectifiers, resistors, and coils, but also for compression molding.
実施例1乃至3と比較例 以下本発明を実施例にもとづいて説明する。Examples 1 to 3 and comparative examples The present invention will be explained below based on examples.
!M1表の配合表に従って材料を配合、混合、混練して
エポキシ樹脂成形材料を得、トランスファー成形機を用
いて金型温度175℃、成形圧力50−1硬化時間3分
間でハイブリッドICを封止成形した。! Compound, mix, and knead the materials according to the recipe in Table M1 to obtain an epoxy resin molding material, and seal and mold a hybrid IC using a transfer molding machine at a mold temperature of 175°C, molding pressure of 50-1, and curing time of 3 minutes. did.
第1表
部
注
411 エポキシ当量220、軟化点80゛Cのエポキ
シ樹脂。Table 1 Note 411 Epoxy resin with an epoxy equivalent of 220 and a softening point of 80°C.
米2 水酸基当量104、軟化点87°Cのフェノール
樹脂。Rice 2 A phenolic resin with a hydroxyl equivalent of 104 and a softening point of 87°C.
来ス 実施例1乃至3についてはセラミックファイバー
表面をアミノシラン糸カップリング剤で表面処理してか
ら用いた。In Examples 1 to 3, the surface of the ceramic fiber was treated with an aminosilane thread coupling agent before use.
第 2 表
注
米 封止品を300“Cで10秒間半田処理後、PCT
試験で151°C,Zoo%湿度内でアルミニウム線の
腐食する迄の時間をみた。Table 2 Note: After soldering the sealed product at 300"C for 10 seconds, PCT
In the test, the time required for aluminum wire to corrode at 151°C and Zoo% humidity was measured.
本発明は上述した如く構成されている。特許請求の範囲
第1項に記載した構成を有するエポキシ樹脂成形材料に
おいては耐湿性が向上する効果を有している。The present invention is constructed as described above. The epoxy resin molding material having the structure described in claim 1 has the effect of improving moisture resistance.
又、特許請求の範囲第2項に記載した構成を有するエポ
キシ樹脂成形材料においては、耐湿性が著るしく向上す
る効果を有している。Furthermore, the epoxy resin molding material having the structure described in claim 2 has the effect of significantly improving moisture resistance.
Claims (1)
剤、硬化促進剤、離型剤、着色剤、カップリング剤、充
填剤等の添加剤を添加してなるエポキシ樹脂成形材料に
おいて、直径1〜10ミクロン、長さ10〜150ミク
ロンのセラミックファイバーの表面をシラン系カップリ
ング剤で表面処理してから含有したことを特徴とするエ
ポキシ樹脂成形材料。(2)セラミックファイバーの量
がシリカ100重量部に対して5〜50重量部であるこ
とを特徴とする特許請求の範囲第1項記載のエポキシ樹
脂成形材料。(1) In an epoxy resin molding material made by adding additives such as a crosslinking agent, a curing agent, a curing accelerator, a mold release agent, a coloring agent, a coupling agent, and a filler to an epoxy resin as necessary, An epoxy resin molding material containing ceramic fibers having a diameter of 1 to 10 microns and a length of 10 to 150 microns after surface treatment with a silane coupling agent. (2) The epoxy resin molding material according to claim 1, wherein the amount of ceramic fiber is 5 to 50 parts by weight based on 100 parts by weight of silica.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP800788A JPH01185321A (en) | 1988-01-18 | 1988-01-18 | Epoxy resin molding material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP800788A JPH01185321A (en) | 1988-01-18 | 1988-01-18 | Epoxy resin molding material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01185321A true JPH01185321A (en) | 1989-07-24 |
Family
ID=11681297
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP800788A Pending JPH01185321A (en) | 1988-01-18 | 1988-01-18 | Epoxy resin molding material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01185321A (en) |
-
1988
- 1988-01-18 JP JP800788A patent/JPH01185321A/en active Pending
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