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JPS59204614A - Molding material for sealing semiconductor part - Google Patents

Molding material for sealing semiconductor part

Info

Publication number
JPS59204614A
JPS59204614A JP7982283A JP7982283A JPS59204614A JP S59204614 A JPS59204614 A JP S59204614A JP 7982283 A JP7982283 A JP 7982283A JP 7982283 A JP7982283 A JP 7982283A JP S59204614 A JPS59204614 A JP S59204614A
Authority
JP
Japan
Prior art keywords
molding material
resin
component
catalyst
essential component
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP7982283A
Other languages
Japanese (ja)
Inventor
Shigeki Ichimura
茂樹 市村
Keiichi Kinashi
木梨 恵市
Etsuji Kubo
久保 悦司
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Resonac Corp
Original Assignee
Hitachi Chemical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hitachi Chemical Co Ltd filed Critical Hitachi Chemical Co Ltd
Priority to JP7982283A priority Critical patent/JPS59204614A/en
Publication of JPS59204614A publication Critical patent/JPS59204614A/en
Pending legal-status Critical Current

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

Abstract

PURPOSE:A molding material for sealing semiconductor devices, consisting of a fine powdered and compressed binary system containing specific components, and having improved pot life and retained curability and other characteristics. CONSTITUTION:A molding material, containing (A) an epoxy resin, e.g. glycidyl ether of bisphenol A or polyethylene glycol, etc., (B) a novolak type phenolic resin, e.g. a resin prepared by condensing and dehydrating a phenol with HCHO, as a curing agent, (C) a catalyst, e.g. 2-methylimidazole or benzyldimethylamine, and (D) a filler, e.g. silica or clay, and obtained by incorpoarating the component (A) in (i) a component system, incorporating >=10wt% component (B) and the component (C) in (ii) a component system as essential components, mixing the respective systems (i) and (ii) at the softening points of the respective component resins or above under melting, pulverizing the resultant mixture into fine powder, and compressing and compacting the resultant fine powdered material containing the uniformly dispersed systems (i) and (ii) at >=0.8 compression ratio.

Description

【発明の詳細な説明】 本発明にポットライフに優nた、電子部品封止成形用エ
ポキシ樹脂成形材料に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an epoxy resin molding material for encapsulating electronic components, which has an excellent pot life.

エポキシ樹脂に、耐湿性、電気特性1機械時性に優nて
いるため、電気絶縁材料として広く用いらnている。神
に、トランジスタ、グイオード、果槓回路lどの牛専俸
袈直の樹脂封止に2いては、高置の耐湿性、電気特性が
必女であシ、エポキシ樹脂、硬化剤としてポリアミン、
無水酸、ノボラック型フェノール側+IM yzと、元
項材としてシリカを王な成分とした低圧移送成形用エポ
キシ樹脂m酸物力S王に用いら1している。
Epoxy resins have excellent moisture resistance, electrical properties, and mechanical properties, so they are widely used as electrical insulating materials. In particular, when it comes to resin sealing of transistors, guide circuits, etc., high moisture resistance and electrical properties are essential, epoxy resin, polyamine as a hardening agent, etc.
Acid anhydride, novolac type phenol side + IM yz, and epoxy resin for low pressure transfer molding with silica as the main component are used for acidic power S king.

しかし、エポキシ樹脂組Iii、qa rx一般にホッ
トラインに劣るため輸送および保管にあたり冷蔵庫が必
要であり、他の熱硬性樹脂組成物たとえば不飽和ポリエ
ステル樹脂、ジアリル2タレート樹脂、フェノール樹脂
と比べ極めて扱いが姐かしい。また、こ匙ら保存安定性
に良い樹脂fl″I峙性に劣るため、牛導体装匝の封止
用とじてにごく一部にしか用いることができない現状に
6る。
However, epoxy resin compositions III and QARX are generally inferior to hotlines and require a refrigerator for transportation and storage, and are extremely difficult to handle compared to other thermosetting resin compositions such as unsaturated polyester resins, diallyl di-thalerate resins, and phenolic resins. It's weird. In addition, the resin fl''I, which has good storage stability, is inferior in properties, so it can currently only be used in a limited number of applications, such as for sealing pouches containing conductors.

一方、エポキシ樹脂組成物のポットライフを改良する方
法として、エポキシ樹脂を硬化剤孕恢械的に粉体′a@
するいわゆるトライブレンド製法は良く知らγしている
。し刀ル、トライブレンド製茫により作らnた成形材料
に、樹脂と硬化卸jが分晴しているため硬化性が者しく
遅くなり式らに光顎材に用いた勾曾に1目脂と充填材の
めnが不元分なためlAαが惑〈また特注も低下するl
との欠点があ夛、特性向から実用に供ぜらnないもので
あった。以上の理由から、千尋体装置封止用エポキシ4
幻脂成形材料に、ミキシンクロールや押出機などの混曾
機葡用いて全組成物を浴融混合して作らnるのが一般的
で必p1この製造法にともないポットラインの低下にや
むに得ないものであった。
On the other hand, as a method for improving the pot life of epoxy resin compositions, epoxy resins are mechanically powdered with a hardening agent.
The so-called tri-blend manufacturing method is well known. Since the molding material made from tri-blend tin is divided into resin and hardening agent, the curing properties are considerably slow, so it is necessary to use one eye resin in the molding material used for the light jaw material. and lAα is confusing because n of the filler is an elemental component (Also, custom orders also decrease l
It had a number of drawbacks, and its characteristics made it unsuitable for practical use. For the above reasons, epoxy 4 for sealing the Chihiro Body Apparatus
It is common to make phantom resin molding materials by bath-melting the entire composition using a mixing machine such as a mixer roll or an extruder. It was something I couldn't get.

不発E!Aは以上の問題点について鋭意検討した相来、
1式γしたものでろバポットラインと特性の相方ン光分
に誘足できる成形材料を提供するものである。
Unexploded E! A has carefully considered the above issues, and
The object is to provide a molding material which can attract the characteristic compatibility with the lobe pot line with the formula 1.

不発明はエポキシ樹Bぼ、(b)硬化剤としてのノボラ
ック型フェノール樹脂、(C)触媒及び(d)充填材を
必須成分とする電子部品封止用成形材料において、該成
形材料に(1)と(II)の2糸の均一に分散した微粉
状物が圧縮比0.8以上に圧端ち密化さnたものであり
、かつ(1)rJエポキシ樹脂ケ必須成分としくIt)
にノボラック型フェノール側側の10皇童%以上と触媒
に必須成分としてふ・す、工 かつ(11)、 (1)ともその成分の樹脂の軟(ヒ点
以よの湿度で浴融混合さtた後倣粉化さnたく)のであ
ること孕%倣とし、得らfした成形材料に、全部葡俗/
1i!混台して作った成形材料よりホットラインに良好
であシ′また、硬化性や有性も良好なものである。
The non-invention is a molding material for encapsulating electronic components, which contains an epoxy tree B, (b) a novolac type phenolic resin as a hardening agent, (C) a catalyst, and (d) a filler as essential components. ) and (II), which are uniformly dispersed fine powder, are densified at the compressed end to a compression ratio of 0.8 or more, and (1) RJ epoxy resin is an essential component.
10% or more on the novolac-type phenol side and fusu as an essential component of the catalyst. After pulverization, the resulting molding material is completely powdered.
1i! It is better on the hot line than molding materials made by mixing, and also has better curing properties and properties.

なお硬化剤としてジアミノジフェニルメタンやジアミノ
ジフェニルスルホンのようなポリアミン類、さらに′r
 HP AやB TD Aのようl無水酸類は、微粉化
した場せホットンイ2に劣る傾向孕示し、本発明V′c
分ける硬化剤として用いることにできないが、ノボ2ツ
タ型ンエノール樹脂欠用いた揚台にに、40iで6μ日
俊の流動住珠持率は80%と良好である。
As a curing agent, polyamines such as diaminodiphenylmethane and diaminodiphenylsulfone, and also 'r
Acid anhydrides such as HP A and BTD A tend to be inferior to Hotton 2 when micronized, and the present invention V'c
Although it cannot be used as a curing agent, the fluid retention rate of 40i and 6μ Nitsun is as good as 80% when used on a platform that does not use enol resin.

さらにに化剤としてノボラック型ンエノール納脂勿用い
た搦付、(υ系にノボラック型フェノール樹脂茹入γL
ることができる。丁lわち、エボキシイ立グハ首とノボ
ラック型ンーノール樹脂だけでにほとんど反応しないた
め、ポットラインに低下せず、浴融混合時のと「莱牲等
の鋭意から(1)糸にフェノール樹脂葡人rしることが
可能である。
In addition, as a curing agent, novolac-type phenolic resin was added without using fat, (γL with novolac-type phenol resin boiled in the υ system).
can be done. In other words, since there is almost no reaction between the epoxy resin and the novolak-type resin, it does not drop to the pot line, and when mixing in the bath melt, (1) phenolic resin is added to the thread. It is possible to know someone.

たたし、(男系が触媒たけKなると叩糸の童が極端に少
なくなり、(1)系と(11)系の均−混せが難かしく
なるため、ンエノール樹脂の10%以上塗(11)糸に
用いることが心太である。
However, (if the male line has a catalyst level of K, the number of children in the beating thread will be extremely small, and it will be difficult to mix the (1) system and (11) system evenly, so apply more than 10% of the enol resin (11). ) It is shinta that is used for thread.

また、成形材料とじては、倣粉状物老タブレットもしぐ
a顆粒状に正補し、?l)密化するCとが球扱よと脱気
の点で望ましく、圧縮比(組成物比止/峻化物比貞)=
0.8以上まで機械的に圧端しち缶化してυ〈ことか心
安である。このと@微粉状物の粒度は盆前の50X鍛%
以上が44μ以下であり、力・つ100μ以上のものが
重重2%以下で必るCとが好lしい0微粉化しすぎると
ポットライフが低下する。
In addition, as for molding materials, imitation powder tablets can also be corrected into granules. l) Dense C is desirable from the viewpoint of degassing when handling balls, and the compression ratio (composition ratio/composition ratio) =
It is safe to know that the pressure end can be mechanically reduced to 0.8 or higher. In this case, the particle size of the fine powder is 50X forging% before the tray.
It is preferable that C is 44μ or less, and that the weight and weight is 2% or less with a force and strength of 100μ or more.If the powder is pulverized too much, the pot life will be reduced.

本発明で用いることができるエポキシ情脂としてはたと
えば、ビスフェノールA、ビスフェノールFルゾルシノ
ール、フェノールノボシック、クレゾールノボラックな
どのフェノール類のグリジルエーテル、ブタンジオール
、ポリエチレングリコール、ポリエチレングリコールな
どのアルコール類のダリシジルエーテル、2タル酸 イ
ソフタル酸、テトジヒドロフタル酸などのカルボン酸類
のグリシジルエステルなどのグリシジル型エポキシ樹脂
、分子内のオシ2イン粕曾葡過ぼ寺でエポキシ化して侍
らnるいわゆる月言環型エポキシドなどがある。
Examples of epoxy resins that can be used in the present invention include glycyl ethers of phenols such as bisphenol A, bisphenol F lusorcinol, phenol novosic, and cresol novolac, and alcohols such as butanediol, polyethylene glycol, and polyethylene glycol. Glycidyl-type epoxy resins, such as glycidyl esters of carboxylic acids such as dithalic acid, isophthalic acid, and tetodihydrophthalic acid, are epoxidized at the inside of the molecule to form the so-called moon ring. There are mold epoxides, etc.

硬化剤として用いるノボラック型フェノール樹脂とじて
に、フェノール、クレゾール、キシレノール等のフェノ
ール類とホルマリンあるいにバラホルムアルデヒドを酸
性触媒の存在下で縮合反応、脱水させて侍らnf:、も
のが、一般的である。
In addition to the novolak type phenolic resin used as a curing agent, it is generally made by condensing phenol, cresol, xylenol, etc. with formalin or paraformaldehyde in the presence of an acidic catalyst and dehydrating it. It is.

また硬化剤の便用]−エポキシドの1当童に対して0.
5〜1.5当量が好ましく、この範囲?越えると硬化性
および特注が者しく低下する。
Also, use of hardening agent] - 0.00 for 1 epoxide.
5 to 1.5 equivalents are preferred, and this range? If this is exceeded, the hardenability and customization properties will be significantly reduced.

触媒としでに、2−メチルイミダゾール、2エテル−4
−メチルイミダゾールなどのイミダゾール類、ベンジル
ジメチルアミン、トリスジメチルアミンメチルフェノー
ルなどのアミン類、トリフェニルホス2イン、トリブチ
ルホスフィン、テトラフェニルホスホニウムテトラフェ
ニルホレートなどのリン化合物知など、従米知らnてい
るもの孕用いることができ、(男系にさnる。配付光横
材としてはシリカ、クレー、アルミナ、鎖酸バリウム、
マイカ粉、水利アルミナ、ウオラストナイト等の粉体無
機*’に用いることができ、シリカ粉が好ましいもので
ある。
As a catalyst, 2-methylimidazole, 2-ether-4
-Imidazoles such as methylimidazole, amines such as benzyldimethylamine, trisdimethylaminemethylphenol, phosphorus compounds such as triphenylphos-2-yne, tributylphosphine, and tetraphenylphosphonium tetraphenylfolate, etc. Materials can be used for pregnancy (in the male lineage).Silica, clay, alumina, barium chain acid,
It can be used for powdered inorganic*' such as mica powder, water-containing alumina, and wollastonite, with silica powder being preferred.

光填材の(I)および(n)系への分割方法に、そnぞ
tの糸に浴融混合でさる範囲であγしは時に制約さ匙る
ものでにないが、(IJ系になるべく多量に用いる方が
好ましく、(n)系Kl’ff全く入rtrx<てもよ
い。
The method of dividing the optical filler into the (I) and (n) systems is sometimes limited by bath-melting the yarns, but the (IJ system) It is preferable to use as much as possible, and (n) system Kl'ff may be completely used.

妊らに本発明の成形材料には有色剤、離型剤、1必すに
応じC用いることができる。cnら冷カロ剤の(i)お
・よび(11)系への分割方法にとぐに制約さnるもの
でにないが、カップリング炸」げ光填材貢にあ・おむね
比例させることが好lしく、その他についてに樹脂と硬
化剤の址におお・むtu比例させることが好ましい。
In addition, a coloring agent, a mold release agent, and C may be used in the molding material of the present invention as necessary. Although there are no immediate restrictions on the method of dividing the cold caustic agent into the (i) and (11) systems, it is important to make the coupling explosion roughly proportional to the optical filler contribution. It is preferable to make the other factors proportional to the amount of resin and curing agent.

以下実施例匍もって具体的に直曲する0表1 組城表 (1)  クレゾールノボラック型エボキ/欄脂、当M
230.軟化点77℃(日本テパガイギー社商品名へ (2)ノボラック型フェノール樹脂、当量106.軟化
点85℃(日立化成工業商品名) (3)溶融シリカ粉(龍森商品名)。
The following is an example of a concrete straight bending table 1.
230. Softening point: 77°C (Japan TepaGeigy Co., Ltd. trade name) (2) Novolac type phenolic resin, equivalent weight 106. Softening point: 85°C (Hitachi Chemical trade name) (3) Fused silica powder (Tatsumori trade name).

(4)  γ−グリシドキシグロビルトリメトキシシ2
ン実流物−1 表1vc示す組成を1−(1)Bよび1−(損に分け、
そnぞAkg0℃のミキシングロールで5分間溶融混台
した後、シート状で取シ出し冷却した。
(4) γ-glycidoxyglobiltrimethoxy 2
Divide the composition shown in Table 1vc into 1-(1)B and 1-(loss).
After melting and mixing on a mixing roll at 0° C. for 5 minutes, the mixture was taken out in the form of a sheet and cooled.

1−(1)および1−(II)に粗粉砕した後V型プレ
ンダーで混合した。次にビンミル(アルビ不社製コルプ
レックス160Z型)k用い7400rpmで倣粉砕し
たところ粒度に100μ以上のものに1(44μ以下の
ものが78%以上であった。
After coarsely pulverizing 1-(1) and 1-(II), they were mixed in a V-type blender. Next, when it was copy-pulverized at 7400 rpm using a bottle mill (Colplex 160Z model manufactured by Albi Fusha Co., Ltd.), the particle size was found to be 1 for particles of 100 μm or more (78% or more of particles of 44 μm or less).

式らに圧縮比0.85に加圧しタブレット化し、成形に
供した。
The mixture was pressurized to a compression ratio of 0.85 to form a tablet, which was then subjected to molding.

実施例2 実施例1と同様の方法で材料?I−作製した。Example 2 material in the same manner as in Example 1. I-produced.

100μ以上のものに7z(,44μ以下のものが81
%でめった。こnも圧縮比0.86に加圧しタブレット
化した。
7z for items over 100μ (81 for items under 44μ)
% was rare. This was also compressed to a compression ratio of 0.86 and made into tablets.

:に:流物6 、り−(kl)H177スコi用Zてi 40°Cr2
O分…」溶融混合した後冷却し粗粉砕した。その他に実
施例−1と同様な方法で材料葡汗装した0100μ以上
のものはなく、44μ以トのものが89%であった。こ
nも圧縮比0.86でダブレット化し成形に供した。
:ni:Ryubutsu 6, Ri-(kl)H177Scoi Zitei 40°Cr2
After melting and mixing, the mixture was cooled and coarsely ground. In addition, there was no material with a thickness of 0100μ or more that was coated in the same manner as in Example 1, and 89% of the materials had a thickness of 44μ or more. This product was also made into a doublet at a compression ratio of 0.86 and subjected to molding.

実施例4 実施例6と同じ方法で材′+−+忙rμ製した0100
μ以上のものか0,6%、44μ以下のものが60%で
あったoct″Lも圧治6比0.85でタブレット化し
成形に供した0 比較例1 表IK示す組成葡90℃のミキシングロールで5分間浴
融油付した後冷却し粗粉砕しグこ0さらに圧縮比0.8
2でタブレット化し、成形に供した。
Example 4 0100 manufactured by the same method as Example 6
oct''L, which had 0.6% of the content of 0.6% or more than μ or 60% of the content of 44μ or less, was also tabletted at a pressure ratio of 0.85 and subjected to molding.Comparative Example 1 The composition shown in Table IK was After being coated with bath melted oil for 5 minutes with a mixing roll, it is cooled and coarsely pulverized, and the compression ratio is 0.8.
The mixture was made into a tablet using Step 2 and subjected to molding.

表2 特性表 表2vc示した特性について腕曲する。Table 2 Characteristics table Arm bending for the characteristics shown in Table 2vc.

特性測定用の試駅片に% 180℃で2分硬化の条件で
移送成形法で成形した後、180℃で5時10」俊硬化
葡行なった。体積抵抗率に、100m1llφ−5mm
 iの円板孕用い、JIS  K6911に準じて測定
した。またPC’lJグレッシャークッーカーテストの
略でめシ、120℃水蒸気中で100時間の処理ン行な
った0ガラス転移幅度は、熱彰走曲想の変曲点よシ求め
た0ゲルタイムに、JSR型熟吸化性樹脂川キ用ラスト
メータ(今中機械工条製)を用い、180℃−で測定し
た。スパイラルフロー1’ff、El’vll金諒塗用
い18q℃で注入圧カフ0kg/dで測犀した0実施例
1〜4の谷材料のホットライフにきわめて良好であシ、
こrL−tでのエホキシ伺脂成形材料とじては考えらn
ないものであるOaらに。
A test piece for measuring properties was molded by a transfer molding method under the conditions of curing at 180°C for 2 minutes, and then rapidly curing at 180°C for 5:10 minutes. For volume resistivity, 100ml1llφ-5mm
Measurement was performed according to JIS K6911 using a disc of i. Also, PC'lJ Glacier Cooker Test is an abbreviation for the 0 glass transition width after 100 hours of treatment in steam at 120°C. The measurement was carried out at 180° C. using a JSR type long-absorbing resin rust meter (manufactured by Imanaka Machinery Co., Ltd.). The hot life of the valley materials of Examples 1 to 4 was very good when measured at 18q°C using spiral flow 1'ff and El'vll Kinryo coating with an injection pressure cuff of 0 kg/d.
I can't think of an epoxy resin molding material for L-t.
Oa et al.

カラス転移塩度や、電気物性も促米製法材とI”J等で
めp1不発明による電子部品刺止用成形材料に、ポット
ライフと物性の両立した成形材料としてM用である。
The glass transition salinity and electrical properties are also improved by the rice-manufacturing method, I''J, etc., and it is used as a molding material for pricking electronic parts by the P1 invention, and as a molding material that has both pot life and physical properties.

Claims (1)

【特許請求の範囲】 1、  (a)−r−ボキシ樹脂、(b)硬化剤として
のノボラック型フェノール樹脂、(C)触媒及び(aJ
光横材を必須成分とする電子部品封止用成形材料に2い
て、該成形材料に(1)と(n)の2糸の均一に分散し
た微粉状物が圧動比0.8以上に圧縮ち密化gnfCも
のであり、かつ(I)にエポキシ樹脂塗必須成分としく
損にノボラック型フェノール樹脂の10厘駕%以上と触
媒全必須成分としておシ、かつ(1)、叩ともその成分
の樹脂の軟化点以上の謁贋で俗融混曾さnた後微粉化さ
nたものであることに狗倣とする電子部品封止用成形材
料。 2、  @粉状物の粒度が、100μ以上のものが2」
童%以下であシ、44μ以下のもの&’s 。 皇童%以上である時計請求の範囲第1項に載の電子部品
封止用成形材料。
[Claims] 1. (a) -r-boxy resin, (b) novolac type phenol resin as a curing agent, (C) catalyst and (aJ
2. A molding material for encapsulating electronic parts that has a light cross material as an essential component has two threads (1) and (n) uniformly dispersed in the molding material with a pressure-to-dynamic ratio of 0.8 or more. It is a compressed densified GNFC material, and (I) is coated with epoxy resin as an essential component, and contains 10% or more of novolac type phenolic resin as an essential component of the catalyst, and (1) as an essential component. A molding material for encapsulating electronic parts, which is made by mixing with resin at a temperature above the softening point of the resin and then pulverizing it. 2. @Powder particles with a particle size of 100μ or more are 2.
Items with a diameter of 44μ or less. The molding material for encapsulating electronic components according to claim 1 of the watch claim, which has a molding material of at least 10%.
JP7982283A 1983-05-07 1983-05-07 Molding material for sealing semiconductor part Pending JPS59204614A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7982283A JPS59204614A (en) 1983-05-07 1983-05-07 Molding material for sealing semiconductor part

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7982283A JPS59204614A (en) 1983-05-07 1983-05-07 Molding material for sealing semiconductor part

Publications (1)

Publication Number Publication Date
JPS59204614A true JPS59204614A (en) 1984-11-20

Family

ID=13700895

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7982283A Pending JPS59204614A (en) 1983-05-07 1983-05-07 Molding material for sealing semiconductor part

Country Status (1)

Country Link
JP (1) JPS59204614A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61272260A (en) * 1985-05-29 1986-12-02 Unitika Ltd Minute spherical resin composition and production thereof
WO2012017571A1 (en) * 2010-08-05 2012-02-09 住友ベークライト株式会社 Functional particle, group of functional particles, filler, resin composition for electronic part, electronic part, and semiconductor device
JP2020100824A (en) * 2018-12-20 2020-07-02 三星エスディアイ株式会社Samsung SDI Co., Ltd. Tableted epoxy resin composition for encapsulation of semiconductor devices, and semiconductor device encapsulated using the same

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61272260A (en) * 1985-05-29 1986-12-02 Unitika Ltd Minute spherical resin composition and production thereof
WO2012017571A1 (en) * 2010-08-05 2012-02-09 住友ベークライト株式会社 Functional particle, group of functional particles, filler, resin composition for electronic part, electronic part, and semiconductor device
JP2012052089A (en) * 2010-08-05 2012-03-15 Sumitomo Bakelite Co Ltd Functional particle, filler, resin composition for electronic part, electronic part, and semiconductor device
JP2012052088A (en) * 2010-08-05 2012-03-15 Sumitomo Bakelite Co Ltd Composition and method for producing the same, filler, resin composition for electronic part, electronic part, and semiconductor device
JP2012052087A (en) * 2010-08-05 2012-03-15 Sumitomo Bakelite Co Ltd Functional particle group, filler, resin composition for electronic part, electronic part, and semiconductor device
JP2012052090A (en) * 2010-08-05 2012-03-15 Sumitomo Bakelite Co Ltd Functional particle and its manufacturing method, filler, resin composition for electronic component, electronic component, and semiconductor device
CN103052687A (en) * 2010-08-05 2013-04-17 住友电木株式会社 Functional particle, group of functional particles, filler, resin composition for electronic part, electronic part, and semiconductor device
JPWO2012017571A1 (en) * 2010-08-05 2013-09-19 住友ベークライト株式会社 Functional particle, functional particle group, filler, resin composition for electronic component, electronic component and semiconductor device
TWI504653B (en) * 2010-08-05 2015-10-21 Sumitomo Bakelite Co Functional particle and mixture thereof, filler, resin composition for electric component and semiconductor device using the same
JP2020100824A (en) * 2018-12-20 2020-07-02 三星エスディアイ株式会社Samsung SDI Co., Ltd. Tableted epoxy resin composition for encapsulation of semiconductor devices, and semiconductor device encapsulated using the same

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