JPS5922963A - Manufacture of molding compound for sealing - Google Patents

Manufacture of molding compound for sealing

Info

Publication number
JPS5922963A
JPS5922963A JP13237182A JP13237182A JPS5922963A JP S5922963 A JPS5922963 A JP S5922963A JP 13237182 A JP13237182 A JP 13237182A JP 13237182 A JP13237182 A JP 13237182A JP S5922963 A JPS5922963 A JP S5922963A
Authority
JP
Japan
Prior art keywords
polybutadiene rubber
rubber
kneading
molding compound
curing agent
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
JP13237182A
Other languages
Japanese (ja)
Inventor
Kozo Hirokawa
広川 孝三
Shinsuke Hagiwara
伸介 萩原
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 JP13237182A priority Critical patent/JPS5922963A/en
Publication of JPS5922963A publication Critical patent/JPS5922963A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain titled molding compound with high crack-resistant potential, suitable for sealing electronic parts, by kneading in advance, a thermosetting resin with specific two sorts of polybutadiene rubber and an inorganic filler followed by incorporating the resultant blend with a curing agent and then carrying out a further kneading. CONSTITUTION:The objective molding compound can be obtained, first by kneading (A) 100pts.wt. of a thermosetting resin with (B) 10-30pts.wt. of a polybutadiene rubber with no functional group, in one molecule, other than double bond, (C) 5-10pts.wt. of a second polybutadiene rubber with both terminal hydroxyl and internal epoxy groups, and (D) 200-600pts.wt. of an inorganic filler, followed by incorporating a curing agent in the resulting blend to carry out a further kneading. The former polybutadiene rubber is pref. of a molecular weight 150,000-250,000, with 1,4-cis bond accounting for >=95wt%. The latter polybutadiene rubber is pref. of a molecular weight 2,000-4,000.

Description

【発明の詳細な説明】 今日</J電子機器は、小型軽黛、薄型化が1丁1丁追
求さnてきているが、そflを可能lらしめる(1)は
機器の集積度をいかV(尚めるかにかかっており、この
ことは必然的に搭載部品の小型化指向が−m=−2るこ
とを示すOこのため、成形品υプラスチックSの厚みが
エフ薄く、小さくyzD様々な温度環境下においてクラ
ックが生じ易<Ixりs彪も大切々信頼性が低下する費
因となる。
[Detailed Description of the Invention] Today's electronic devices are being pursued to be smaller, lighter, and thinner, one by one. It depends on whether it is possible to make the molded product υ plastic S thinner and smaller. The tendency for cracks to occur under various temperature environments is also an important cause of reduced reliability.

従って、今俊1すますこりクラック対策が爪安課題にな
ると考えらハる。この対処策として。
Therefore, Shun Ima thinks that countermeasures against cracks will become a major issue. As a workaround for this.

Cn1でいろいろな方法が賦与ら几てきたが、基本的V
Cは、■封止する部品CtJ熱膨汝V(近づける■可焼
性樹脂り通用■ゴム(L)硝加lどが侠討芒nてさたo
しかし、■の方法は光填剤ンθ1率に添加するため成形
材料とし一〇必蒙l猟動性が低下するため一犀の限界か
める。■V〔ついてrJl一般的Vt可廃性樹脂に二次
転移編度が低いu回にあるため、封止した製品り崗腿保
障とり関係で採用しがたい場合がある。一方、■はil
J述り工うlことが少ないというn口釆から、現状でf
:i最良の方策として倹約さnてきている。
Various methods have been provided for Cn1, but the basic V
C is ■ Parts to be sealed CtJ thermal expansion
However, the method (2) has its limits because the optical filler is added to the θ1 ratio, which reduces the mobility of the molding material. ■ Since the secondary transition knitting degree of general Vt disposable resins is in the low u times, it may be difficult to employ it in relation to the security of sealed products. On the other hand, ■ is il
From the viewpoint that there is little to say,
:I have become increasingly frugal as the best policy.

−ロVCゴム添加法といっても、ゴムVtは分子中r(
二厘帖台や極性基全刹するものlどが必り、こ扛らt単
純に添加しmだけでは成形Vt除して、ゴムの齢み出し
、そrL VCよる金型汚n、成形品の外観〈もり、バ
リlどり問題が生じる。
Although it is called the VC rubber addition method, the rubber Vt is r(
A two-layer stand or a device that completely disassembles the polar group is required, but simply adding m alone will reduce the molding Vt, increase the age of the rubber, and cause mold contamination due to VC, and molding. Problems arise with the appearance of the product, such as burrs or burrs.

本発明は、こうした問題点全克服すると共に丁ぐ2’し
た朗クラック性の成形材料を得る組成及び製造法N−)
いて倹約した粕釆Fむtたものである。
The present invention overcomes all of these problems and provides a composition and manufacturing method for obtaining a molding material with low crack resistance.
It is a frugal and frugal kasu pot.

本発明はP硬化性樹脂1oo厘景都に対し。The present invention is directed to a P-curable resin.

分子中VC二ム#J@以外の官能基を有していないポリ
ブタジェンゴム1o〜5oniipm末端V(水m基、
内部Vtエポキシ基に’lfするポリブタジーンゴム5
〜10.1血bt1及び熊磯元横剤2゜O〜600止星
都を言む組JJy、物全あらかじめ混線し、こ(L)混
練物VC6Ji化剤を6加混練することt特徴とする封
止用成形材料の製造法に関する。
Polybutadiene rubber having no functional groups other than VC2M #J@ in the molecule 1o to 5oniipm terminal V (water group,
Polybutadiene rubber with internal Vt epoxy groups 5
~10.1 Blood bt1 and Kumaiso original side agent 2゜O~600 JJy that says Stop Seito, mix everything in advance, and knead this (L) kneaded product VC6Ji agent 6 t Features The present invention relates to a method for producing a molding material for sealing.

本発明で1更ハJさjLる熱硬化性樹脂は、エポキシ4
例月11ノエノールイvtnh、ポリエステル4鮒刀旨
lど−奴り成形材料に用いらnるものが用いらrしる。
The thermosetting resin used in the present invention is epoxy 4
Every month on November 11th, polyester is used as a molding material.

を時足り2独のポリブタジェンゴムを併用すること刀I
杢発明の特畝的lことであるが、そり理由は、口IJ述
した問題点、納」ち、ゴムり参み出し、そrtvt起因
する金型り汚n%成形品の外観〈もり、パリ(イバリ)
lどに対し、極めで効果「ソVC機能するからである。
It is possible to use the same polybutadiene rubber in combination with the sword I.
The reason for the warping is that the heather invention is characterized by the above-mentioned problem, the rubber starting to bulge out, and the appearance of the molded product due to mold stains. Paris (Ibari)
This is because the effect of ``So-VC'' functions in the extreme.

ことに、分子中V(二]1ポd甘以外に官能基を南して
いないポリブタジェンゴムは、善み出しVCよる金型汚
几、成形品外観す〈モクに、木端に水酸基をするポリブ
タジェンゴムはパリにそfLぞlL鳴効であることVC
よる○また添力l血の制限VJ1約1約υ省おリフ゛タ
ジエンゴムtx熱llll7魅試躾の21・6来V(丞
っく有効範囲、俊者りポリブタジェンゴムa別掲するバ
リ(’JILIIJ疋A、a朱による必擬最少艦と最大
硝カ11垣を7J<丁ものである。
In particular, polybutadiene rubber that does not contain any functional groups other than V(2)1 pod in the molecule has hydroxyl groups on the end of the wood, which causes mold stains due to the VC that oozes out, and the appearance of the molded product. The polybutadiene rubber used for this purpose is manufactured in Paris.VC
○Also, the limit of blood pressure VJ1 is approximately 1 υ saving, the tx heat llll 7 is 21.6 V (the effective range, the polybutadiene rubber a is listed separately) 'JILIIJ A, a Zhu's minimum ship and maximum ship 11 fences are 7J < ding.

分子中に二皿結せ以外に官能基金イイしていないポリブ
タジェンゴムとしては分子量か15〜25万、1.4シ
ス型粕台が95部以よりものが好葦しくは用いら7L、
こtしらiJ由販さ2’Lでいる。
Polybutadiene rubber that does not have any functional properties other than two plates in the molecule should preferably have a molecular weight of 150,000 to 250,000, and a 1.4 cis type lees with 95 parts or more, preferably 7L,
I'm 2'L from iJ.

末端r水酸基、内部にエポキシか?有するポリブタジェ
ンゴムとしては分子jii2000〜4000りものが
好1しくは用いらfL、  こnらも市販式nている。
Terminal r hydroxyl group, epoxy inside? The polybutadiene rubber having a molecular weight of 2,000 to 4,000 is preferably used, and these are also commercially available.

こ〕しらのゴムケ彼卸1且つ均−分t49.芒せる方法
は、主成分でめる熱硬化性樹脂と充填剤にゴムの三戟分
系ケ強制的に混線することVCXる剪断力で相互分散し
、得ることができる。
[This] Shira no Gomuke He wholesale 1 and average t49. In this method, a thermosetting resin consisting of the main components and a filler are forcibly mixed in a three-part system of rubber, so that they are mutually dispersed by the shearing force of VCX.

こりゴム分散体は、ミキシングロール、ニーダ−5力1
圧式ニーダ−なと勿使用して混練できる。
The stiff rubber dispersion is prepared using a mixing roll, kneader, 5 forces, 1
Of course, it can be kneaded using a pressure kneader.

充填剤としては、珪石vl、ろ英ガラス初、タルク、珪
藻土、ガラス棟維などが便用さrLるが、−/Cの選択
と光情血は成形方法、封止する部品(素子) Vt L
り決冗さ几る〇 最終り成形伺++を侍るには、ゴム分散体に硬化剤、必
要に比、し期科、離型剤などを饋刀口し。
As a filler, silica, silica glass, talc, diatomaceous earth, glass fiber, etc. are conveniently used, but the selection of -/C and the optics are determined by the molding method and the parts (devices) to be sealed. L
To prepare for the final molding process, add a curing agent, a curing agent, a mold release agent, etc. to the rubber dispersion as necessary.

こり組成物ケミキノングロール、押出式混線磯などVL
Lり俗融混線し、冷肩j固化俊、朋米式粉砕4歳lど音
用いて粉砕する。
VL such as stiff composition Chemikinon Groll, extrusion type mixed wire iso, etc.
It is crushed using the cold shoulder j solidification shun, Homai style crushing 4 years old lud sound.

秘土、耐止用成形制科の製造法について説明してきlこ
が、本発明(/J成形月利はトランスファー戟形圧紬成
形、射出成形などV(十分便用し侍る成形特f+、會南
し、すぐれた耐クラック注tMしている。
This article explains the manufacturing method of the secret molding system for anti-resistance molding. It has excellent crack resistance.

以下本発明を実施例に丞いて説明Tる。The present invention will be explained below with reference to Examples.

実施例 ポリブタジェンゴム(日本ゼオン社製%曲品名二ボール
BR−1220、分子量20万、1゜4シス型紹台98
%以上)10PivS、末端水酸基。
Example Polybutadiene rubber (manufactured by Nippon Zeon Co., Ltd. Product name 2-ball BR-1220, molecular weight 200,000, 1°4 cis type introduction 98
% or more) 10PivS, terminal hydroxyl group.

円flycエポキシ基を有する液状のポリブタジェンゴ
ム(出光石油化学社製、商品名ポリゲタシェフR−45
Epl、分子量2800)5都エボキ7樹脂(日本化桑
社製、商品名EOCN102)100部尤填剤として、
石英ガンス粉(雇森社製、商品名ヒユーズレックスRD
−8)400部’に90〜95℃に加編した力1圧式ニ
ーグーに投入して、60分間混線を付い、取り出し冷却
同化後、粉砕する。削2配りゴム分散体515都、硬化
剤として2エノールノボラツク側脂(軟化点90’C)
40部、硬化助剤(四国化H,社’JI、商品名イミダ
ゾールCItZ)  5都t IIItE型剤としてス
テアリン酸5部、顔料カーボンフラッフ1部を加え、ヘ
ンシェルミキサで60秒IWJ 乾式島台したのち、ミ
キシングロール(ロール60〜65℃、後ロール80〜
85°C1ギヤグ5〜5 num ) VCて10分間
浴融混混練性った。
Liquid polybutadiene rubber having a flyc epoxy group (manufactured by Idemitsu Petrochemical Co., Ltd., trade name Polygetashev R-45)
Epl, molecular weight 2800) 5 to Eboki 7 resin (manufactured by Nippon Kasosha, trade name EOCN102) 100 parts As a filler,
Quartz Guns powder (manufactured by Hiramorisha, trade name: Fuse Rex RD)
-8) Pour 400 parts into a single-pressure Ni-Goo heated at 90 to 95°C, stir for 60 minutes, take out, cool and assimilate, and then crush. Rubber dispersion 515 times, 2-enol novolak side fat as hardening agent (softening point 90'C)
40 parts, curing aid (Shikokuka H, Co., Ltd.'JI, trade name: Imidazole CItZ) 5 parts, 5 parts of stearic acid as a IIItE type agent, and 1 part of pigment carbon fluff were added, and the mixture was subjected to IWJ drying for 60 seconds using a Henschel mixer. Afterwards, mixing roll (roll 60~65℃, rear roll 80~
The mixture was melt-kneaded for 10 minutes at 85°C and 1 gear (5 to 5 num) VC.

冷却固化佐、粉砕して得几戚形材料は問題点であったゴ
ムCI)―み出し、金型汚7L、底形品の外観のくもり
もlく、パリ匹ついても1.5111[11以下(ml
l:in件ll11!6m1oX深す20μのスリット
vt(i(し出した材料の艮δを測定する。金型温度1
80’c、成形圧カフ0kg/atM、形時間90秒)
とそ1しぞfL艮好であった。1だ熱衝撃試験(150
℃のンリコーンオイル=2分間浸漬、液体輩累:2分間
反誠ケ1サイクル)を行う1こめ、金型崗m+so°G
1JD、形圧カフ0kg/an’、R形時IMJ90秒
り条件で試料(7X7XQ、5mmのシリコン系子を1
4X20X2mmlj成形)會作成し、そILケ180
°G、  6時+M+アフターキュアーして供しノこ0 帽来は、500サイクルでもクラッタが発生与らgf丁
ぐn7ζ耐クラツタ性の成形材料であることが雑誌さr
した。
After cooling and solidifying, the molded material obtained by crushing was a problem (rubber CI) - extrusion, mold contamination 7L, the appearance of the bottom molded product was cloudy, and even if there were particles, it was 1.5111 [11 Below (ml
l: in casell11!6m1oX 20μ deep slit vt (i (Measure the δ of the oozed material. Mold temperature 1
80'c, molding pressure cuff 0kg/atM, molding time 90 seconds)
The fL style was the best. 1 Thermal shock test (150
Soak in corn oil at °C for 2 minutes, soak in the liquid for 2 minutes (1 cycle), and soak the mold for 2 minutes.
1 JD, shape pressure cuff 0 kg/an', IMJ 90 seconds for R type, sample (7X7XQ, 5 mm silicone
4X20X2mm molding
°G, 6 o'clock + M + after-cure and 0 The magazine says that it is a clutter-resistant molding material that does not generate clutter even after 500 cycles.
did.

実施例2 ポリブタジェンゴム(日本ゼオンft袈、商品名、二ボ
ールBR1220)20都、敵状ポリブタジェンゴム(
出光石油化学社製二藺品名ポリブタジェンR45Epl
)t3都エボキン41N崩(日本化楽社製 商品名EO
CN l 02 )100m光槙剤として石英ガラス粉
(崩及仕表。
Example 2 Polybutadiene rubber (Nippon Zeon ft., trade name, 2-ball BR1220), 20% polybutadiene rubber (
Product name Polybutadiene R45Epl manufactured by Idemitsu Petrochemical Co., Ltd.
) t3 Miyako Evokin 41N Kotsu (manufactured by Nippon Kagakusha, product name EO)
CN l 02 ) 100 m Quartz glass powder as a light emitting agent (decomposition preparation).

商品名ヒユーズレックスRD−8)400都ケ90〜9
5’Cに刃口崗した加圧式ニーダ−VC投入し、50分
間混株r行い取り出し耐却向化波、粉砕する。
Product name: Fuse Rex RD-8) 400 Miyako 90-9
A pressurized kneader VC with a sharpened blade was placed at 5'C, the mixture was mixed for 50 minutes, and the mixture was taken out and pulverized.

跨U紀のゴム分散体528部VC硬化剤としてフェノー
ルノボ2ツク樹脂(軟化点90’C)40部、硬化助剤
(四国化成社線、商品名イミタノールCry z) s
 hu離型剤としてステアリン酸6部、顔料、カーボン
ブラック1郁を刃口え、実施17′l11と同様の製造
条件で成形材料紮侍た。
528 parts of the rubber dispersion of the straddle period 40 parts of phenol novo 2 resin (softening point 90'C) as a VC curing agent, curing aid (Shikoku Kasei Co., Ltd., trade name: Imitanol Cry z) s
6 parts of stearic acid, a pigment, and 1 part of carbon black were added as a mold release agent, and the molding material was prepared under the same manufacturing conditions as in Example 17'111.

こC1JJD、形材料は実施例1と同前の成形特性(成
形品の外観、パリなど)全示し、筐た、同様り熱衝撃試
験においても600サイクルでもクランクの発生がなか
った。
The molding material of this C1JJD exhibited all the same molding characteristics as in Example 1 (the appearance of the molded product, cracks, etc.), and the casing also showed no cranking even after 600 cycles in the thermal shock test.

比較?l11 アクリロニトリルブタジェンコ゛ム(日本ゼオン社製、
商品名、二ボール+06Z)15部、エポキシ樹脂(日
本化桑社展、商品名EOCN102)100f小光導剤
として石英ガラス粉(龍森社製、商品名ヒユーズレック
スRD−8)400部ケ90〜95℃VC71I]YM
シた加圧式ニーダ−VC投入して30分間混混線性い、
取り出し冷却固化イ没粉砕−J−る○ 前記ゴム分散体515fillVc硬化剤としてフェノ
ールノボラソタ樹脂40都、硬化助剤(四国化成社製、
商品名イミダゾールCl7Z)5部、離型6りとしてス
テアリン酸5部、顔料、カーボンブラック1都會力1え
、爽施秒り1と(yt様C1,J製造条件で成形I科を
狗る。
Comparison? l11 Acrylonitrile butadiene comb (manufactured by Nippon Zeon Co., Ltd.)
15 parts of epoxy resin (Nihonka Kuwasha Exhibition, product name EOCN102), 100 f quartz glass powder as a small light guiding agent (manufactured by Ryumori Co., Ltd., product name Fuse Rex RD-8) 400 parts 95℃VC71I]YM
Pressurized kneader - No crosstalk for 30 minutes after charging VC.
Take out, cool, solidify and pulverize - J-RU○ Rubber dispersion 515fillVc phenol noborasota resin 40 as curing agent, curing aid (manufactured by Shikoku Kasei Co., Ltd.,
Product name: Imidazole Cl7Z) 5 parts, mold release: 6 parts, stearic acid: 5 parts, pigment, carbon black: 1 strength, 1 second: (yt-like C1, J manufacturing conditions).

乙の成形材料ケ実施例1と四条性で成形した粕来、金型
汚n1成形品の外観(もり、加えてパリも5mm以上で
めつ^。但し、熱衝撃試験においてrJ 500サイク
ルでもクラック発生はりらrLなかった。
Molding material of Example 1 and the appearance of the molded product with mold contamination and mold contamination (mold, molded with mold contamination of 5 mm or more). However, in the thermal shock test, cracks were observed even at rJ 500 cycles. There was no outbreak.

比較?l12 エポキシ伺脂(日本化系社製1間品名EOCN102)
+0011を硬化剤としてフェノールノボ(龍蘇社製、
商品名ヒューズレソタスKD−(3)400都、#離型
Δリステアリン庫61β、顔■カーボンブラック18に
へ77工ルミ千丈−V(て60秒秒間式混甘し、実施?
1」1と同僚り製造条件で成形材料inる0 こCIJ成形拐科は実施=iと同等以上の成形特性ケ1
している反面、熱WJ軍試戚V(お・いては、50〜7
0サイクルでクランクが発生した0以上脱明して@7ζ
ように本発明VCおいては、あらかじめゴム全一様V(
分散さぞることV(Lυ、耐クラツク性の丁ぐ1した成
形材料ケ得るVC至り。
Comparison? l12 Epoxy resin (manufactured by Nippon Kakei Co., Ltd. Product name: EOCN102)
Phenol Novo (manufactured by Ryuso Co., Ltd.) using +0011 as a curing agent.
Product Name: Fuse Lesotas KD-(3) 400 Mt. # Release Δ Listearin 61β Face ■ Carbon Black 18 to 77 Lumi Senjo-V (Mix for 60 seconds, conduct?
This CIJ molding department has molding properties equivalent to or better than i.
On the other hand, the hot WJ military trial relative V (O-I is 50-7
A crank occurred in the 0 cycle. After 0 or more, @7ζ
As shown, in the VC of the present invention, the entire rubber uniformity V (
Dispersion of V (Lυ) leads to VC that provides a molding material with excellent crack resistance.

17t I極性基性用しているポリブタジェンコム會併
用するCとでパリなどいわゆる成形−+−i+生を同上
させることがでさ、従来の問題点を牌決′jることがで
きた。
17t I By using C in conjunction with the polybutadiene comb that has a polar group, we were able to solve the problems of the conventional method by making the so-called molded -+-i+ raw material, such as Paris, the same as above. .

Claims (1)

【特許請求の範囲】[Claims] 1、 熱硬化性樹脂+oomitsi’c対し1分子中
に二ム結せ以外に官能基を有していないポリグタジヱン
ゴム全1Q〜60虞量部、末端に水酸基を部VCエポキ
シ基を有するピリブタジェンゴム5〜10貞賞部及び無
慎光項剤200〜600皇11都を言む組成物?あらか
じめ混性い こL:/J混練Bmに硬化剤ケ添加混練す
ることを待敢とする封止用成形材料QJ製造法0
1. A total of 1Q to 60 parts of polygtadiene rubber, which has no functional groups other than double bonds in one molecule for the thermosetting resin + oomitsi'c, and has hydroxyl groups and VC epoxy groups at the ends. A composition that says 5 to 10 pyributadene rubber and 200 to 600 pyributadine rubber? Sealing molding material QJ manufacturing method that involves adding and kneading a curing agent to Bm mixed in advance
JP13237182A 1982-07-29 1982-07-29 Manufacture of molding compound for sealing Pending JPS5922963A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13237182A JPS5922963A (en) 1982-07-29 1982-07-29 Manufacture of molding compound for sealing

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13237182A JPS5922963A (en) 1982-07-29 1982-07-29 Manufacture of molding compound for sealing

Publications (1)

Publication Number Publication Date
JPS5922963A true JPS5922963A (en) 1984-02-06

Family

ID=15079802

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13237182A Pending JPS5922963A (en) 1982-07-29 1982-07-29 Manufacture of molding compound for sealing

Country Status (1)

Country Link
JP (1) JPS5922963A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6126671A (en) * 1984-07-13 1986-02-05 Matsushita Electric Works Ltd Sealing molding material and production thereof
JPS61285215A (en) * 1985-06-13 1986-12-16 Matsushita Electric Works Ltd Molding material for electronic parts
JPS61285243A (en) * 1985-06-13 1986-12-16 Matsushita Electric Works Ltd Molding material for electronic parts
JPS61285244A (en) * 1985-06-13 1986-12-16 Matsushita Electric Works Ltd Molding material for electronic parts
JPS6259660A (en) * 1985-09-11 1987-03-16 Japan Synthetic Rubber Co Ltd Phenolic resin composition

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6126671A (en) * 1984-07-13 1986-02-05 Matsushita Electric Works Ltd Sealing molding material and production thereof
JPS61285215A (en) * 1985-06-13 1986-12-16 Matsushita Electric Works Ltd Molding material for electronic parts
JPS61285243A (en) * 1985-06-13 1986-12-16 Matsushita Electric Works Ltd Molding material for electronic parts
JPS61285244A (en) * 1985-06-13 1986-12-16 Matsushita Electric Works Ltd Molding material for electronic parts
JPH0528242B2 (en) * 1985-06-13 1993-04-23 Matsushita Denko Kk
JPS6259660A (en) * 1985-09-11 1987-03-16 Japan Synthetic Rubber Co Ltd Phenolic resin composition

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