JPH0234182B2 - DENSHIBUHINFUSHOSEIKEIZAIRYO - Google Patents

DENSHIBUHINFUSHOSEIKEIZAIRYO

Info

Publication number
JPH0234182B2
JPH0234182B2 JP56069652A JP6965281A JPH0234182B2 JP H0234182 B2 JPH0234182 B2 JP H0234182B2 JP 56069652 A JP56069652 A JP 56069652A JP 6965281 A JP6965281 A JP 6965281A JP H0234182 B2 JPH0234182 B2 JP H0234182B2
Authority
JP
Japan
Prior art keywords
molding material
group
electronic components
polyester resin
unsaturated polyester
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
Application number
JP56069652A
Other languages
Japanese (ja)
Other versions
JPS57184243A (en
Inventor
Muneasa Torii
Tsutomu Hamada
Kenichi Tateno
Masami Yokozawa
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.)
Panasonic Electric Works Co Ltd
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial Co Ltd
Matsushita Electric Works 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 Matsushita Electric Industrial Co Ltd, Matsushita Electric Works Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP56069652A priority Critical patent/JPH0234182B2/en
Publication of JPS57184243A publication Critical patent/JPS57184243A/en
Publication of JPH0234182B2 publication Critical patent/JPH0234182B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L23/00Details of semiconductor or other solid state devices
    • H01L23/28Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection
    • H01L23/29Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection characterised by the material, e.g. carbon
    • H01L23/293Organic, e.g. plastic
    • H01L23/296Organo-silicon compounds
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2924/00Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
    • H01L2924/0001Technical content checked by a classifier
    • H01L2924/0002Not covered by any one of groups H01L24/00, H01L24/00 and H01L2224/00

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は電子部品を封止する成形材料に関する
もので、その目的とするところは加湿時における
表面抵抗率の低下を防止し、電圧印加時の表面漏
れ電流の発生をなくし電子部品の耐湿性を向上せ
しめることにある。 近年、各種電子部品においては、その低コスト
化と生産性向上のため、プラスチツクによる封止
がなされるようになつてきた。これらの電子部品
には例えばトランジスタ等がある。これらプラス
チツクによる封止方法としては、注型、圧縮成
形、射出成形、トランスフアー成形などが用いら
れており、生産性を向上させるため量産性、作業
性に優れた射出、トランスフアー成形法が多用さ
れている。また一般に、これらの電子部品は小型
であり50〜200個取りといつた非常に多数個取り
の成形がなされている。このため、封止用材料に
は多数個取り成形を満足させるためシリコン樹脂
成形材料、エポキシ樹脂成形材料、不飽和ポリエ
ステル樹脂成形材料等の熱硬化性樹脂成形材料が
使用されているがシリコン樹脂成形材料は機械的
強度が低く、金属との密着が弱い欠点があり、エ
ポキシ樹脂成形材料は流れ性の保存安定性が悪
く、冷凍庫に保管することが必要であり、成形作
業等で室温に放置することによつて著しく流れ性
を劣化する欠点があり、不飽和ポリエステル樹脂
成形材料は機械的強度が高く、金属との密着性も
よく更に流れ性の保存性がよく且つ成形性にも優
れているにかかわらず耐湿性が劣るため電子部品
封止用材料としては殆んど使用されていないのが
現状である。本発明者等は電子部品の加湿時にお
ける封止性能を種々検討した結果、不飽和ポリエ
ステル樹脂成形材料に特定の有機シリコン化合物
を添加することによつて耐湿性を著しく向上せし
めることができたので従来適用不可能であつた不
飽和ポリエステル樹脂成形材料の電子部品封止用
分野への適用を可能ならしめたものである。本発
明に用りる特定の有機シリコン化合物の量は特に
限定するものでないが好ましくは0.01〜3重量%
(以下単に%と記す)が望ましい。 本発明は上記の点に鑑みてなされたものであつ
て、機械的強度が高く、金属との密着性がよく、
流れ性の保存性がよく、成形性のよいしかも耐湿
性に優れた電子部品封止用成形材料を得ることが
できたものである。 以下本発明を詳細に説明する。 本発明に係る電子部品封止用成形材料は、イソ
フタル酸.オルソフタル酸.無水フタル酸.コハ
ク酸.アジピン酸.セバチン酸.無水エンドメチ
レンテトラヒドロフタル酸.クロルジン酸などの
飽和二塩基酸と、エチレングリコール.ジプロピ
レングリコール.1.3ブタンジオール.水素化ビ
スフエノール.ネオペンテルグリコール.イソベ
ンテルグリコール.1.6ヘキサンジオールなどの
多価アルコールとマレイン酸.無水マレイン酸.
フマル酸.イタコン酸などの不飽和二塩基酸とを
反応させて得られる不飽和ポリエステル樹脂に対
してスチレン、t−ブチルスチレン.クロロスチ
レン.ジビニルベンゼン.ジアリルフタレート.
ビニルトルエン.アクリル酸エステル類などの不
飽和ポリエステル樹脂と反応する不飽和基を有す
るモノマー又はそのプレポリマーを架橋剤として
加え、更にガラス繊維、金属ウイスカー、炭素繊
維、ケブラー繊維、ポリエステル繊維、ポリアミ
ド繊維、パルプ、アスベスト、珪酸カルシウム、
バライト、マイカ、クレー、セリサイト、アルミ
ナ、硫化モリブデン、炭酸カルシウム、珪酸、塩
基性炭酸マグネシウム、炭酸マグネシウム、水酸
化カルシウム、水酸化アルミニウム、三酸化アン
チモン、タルク、酸化チタン等の充填剤を加え、
更にステアリン酸亜鉛、ワツクス等の離型剤やカ
ーボンブラツク、酸化鉄等の着色剤やtブチルパ
ーオキシベンゾエート、過酸化ベンゾイル等の硬
化開始剤やカツプリング剤等の添加剤からなる不
飽和ポリエス樹脂成形材料に式1で表わされる有
機シリコン化合物を添加してなるものである。有
機シリコン化合物の量は特に限定するものでない
が好ましくは0.01〜3%が望ましい。即ち有機シ
リコン化合物の量が0.01%未満では耐湿性向上効
果が少なくなる傾向にあり、3%をこえると金属
との密着性が低下する傾向にあるからである。 (式1に於てRは水素基.メチル基.フエニル基
を示すが、更に一部のRを水酸基、アミノ基、エ
ポキシ基で変性したものであることが好ましい。
即ち耐湿性向上効果が大きくなる傾向にあるから
である。) 上記のように本発明は、不飽和ポリエステル樹
脂、架橋剤、充填剤、添加剤からなる不飽和ポリ
エステル樹脂成形材料に特定の有機シリコン化合
物を添加してなることを特徴とするものであるか
ら、硬化反応は硬化開始剤の分離を引金として不
飽和基が架橋にあづかるものである。このためエ
ポキシ樹脂成形材料のような付加縮合反応による
硬化に比べ室温で安定なため、保存性がよい。又
架橋剤により成形時の流れ性を向上せしめること
ができるのでトランスフアー成形や射出成形によ
る電子部品の多数個取りの成形に適することは勿
論、注形、圧縮成形にも適用でき、又特定の有機
シリコン化合物たとえば、前記の式〔1〕の末端
または、側鎖のRはメチル基、フエニル基を示
し、これらRの一部が水素基、水酸基に置き換え
られたものまたは、アミノ基、エポキシ基で変性
されたもので、具体的には、水素基変性シリコー
ン、シラノール変性シリコーン、アミノ変性シリ
コーン、エポキシ変性シリコーンなどにおいて
は、水素基、または、水酸基、アミノ基、エポキ
シ基の反応基が不飽和ポリエステル樹脂のビニル
基と反応することにより耐湿性を向上せしめるこ
とができたものである。 次に本発明を実施例と比較例により具体的に説
明する。 実施例 1乃至5 イソフタル酸1モル、フマール酸1モル、プロ
ピレングリコール2.2モルを反応させて得た不飽
和ポリエステル樹脂を用い第1俵の配合俵に従つ
て配合、混合、混練して電子部品封止用成形材料
を得た。
The present invention relates to a molding material for sealing electronic components, and its purpose is to prevent a decrease in surface resistivity during humidification, eliminate surface leakage current when voltage is applied, and improve the moisture resistance of electronic components. The goal is to improve. In recent years, various electronic components have been encapsulated with plastic in order to reduce costs and improve productivity. These electronic components include, for example, transistors. Casting, compression molding, injection molding, transfer molding, etc. are used as sealing methods with these plastics, and injection and transfer molding methods, which are superior in mass production and workability, are often used to improve productivity. has been done. Generally, these electronic components are small and are molded in a large number of molds, such as 50 to 200 molds. For this reason, thermosetting resin molding materials such as silicone resin molding materials, epoxy resin molding materials, and unsaturated polyester resin molding materials are used as sealing materials to satisfy multi-cavity molding. The material has the disadvantage of low mechanical strength and weak adhesion to metals, and epoxy resin molding materials have poor flowability and storage stability, so they must be stored in the freezer and left at room temperature during molding operations. However, unsaturated polyester resin molding materials have high mechanical strength, good adhesion to metals, and have good flowability, long shelf life, and excellent moldability. However, it is currently hardly used as a material for encapsulating electronic components because of its poor moisture resistance. As a result of various studies on the sealing performance of electronic components during humidification, the present inventors were able to significantly improve the moisture resistance by adding a specific organic silicon compound to the unsaturated polyester resin molding material. This makes it possible to apply unsaturated polyester resin molding materials to the field of encapsulating electronic components, which was previously impossible. Although the amount of the specific organosilicon compound used in the present invention is not particularly limited, it is preferably 0.01 to 3% by weight.
(hereinafter simply referred to as %) is desirable. The present invention has been made in view of the above points, and has high mechanical strength, good adhesion to metal,
It was possible to obtain a molding material for encapsulating electronic components that has good flowability, good storage stability, good moldability, and excellent moisture resistance. The present invention will be explained in detail below. The molding material for encapsulating electronic components according to the present invention contains isophthalic acid. Orthophthalic acid. Phthalic anhydride. Succinic acid. Adipic acid. Sebacic acid. Endomethylenetetrahydrophthalic anhydride. Saturated dibasic acids such as chlordic acid and ethylene glycol. Dipropylene glycol. 1.3 Butanediol. Hydrogenated bisphenol. Neopentyl glycol. Isobentel glycol. 1.6 Polyhydric alcohols such as hexanediol and maleic acid. maleic anhydride.
Fumaric acid. An unsaturated polyester resin obtained by reacting an unsaturated dibasic acid such as itaconic acid with styrene, t-butylstyrene. Chlorostyrene. Divinylbenzene. Diaryl phthalate.
Vinyl toluene. A monomer or its prepolymer having an unsaturated group that reacts with unsaturated polyester resins such as acrylic esters is added as a crosslinking agent, and furthermore, glass fiber, metal whisker, carbon fiber, Kevlar fiber, polyester fiber, polyamide fiber, pulp, asbestos, calcium silicate,
Adding fillers such as barite, mica, clay, sericite, alumina, molybdenum sulfide, calcium carbonate, silicic acid, basic magnesium carbonate, magnesium carbonate, calcium hydroxide, aluminum hydroxide, antimony trioxide, talc, titanium oxide, etc.
Furthermore, unsaturated polyester resin molding is made of mold release agents such as zinc stearate and wax, coloring agents such as carbon black and iron oxide, curing initiators such as t-butyl peroxybenzoate and benzoyl peroxide, and additives such as coupling agents. It is made by adding an organic silicon compound represented by formula 1 to the material. Although the amount of the organosilicon compound is not particularly limited, it is preferably 0.01 to 3%. That is, if the amount of the organic silicon compound is less than 0.01%, the effect of improving moisture resistance tends to decrease, and if it exceeds 3%, the adhesion to metal tends to decrease. (In formula 1, R represents a hydrogen group, a methyl group, or a phenyl group, but it is preferable that a part of R is further modified with a hydroxyl group, an amino group, or an epoxy group.
That is, this is because the effect of improving moisture resistance tends to be greater. ) As mentioned above, the present invention is characterized by adding a specific organic silicon compound to an unsaturated polyester resin molding material consisting of an unsaturated polyester resin, a crosslinking agent, a filler, and an additive. The curing reaction is triggered by separation of the curing initiator, and unsaturated groups participate in crosslinking. Therefore, it is more stable at room temperature than curing by addition condensation reaction such as epoxy resin molding materials, and has good storage stability. In addition, since the flowability during molding can be improved by a crosslinking agent, it is suitable for molding multiple electronic parts by transfer molding and injection molding, and can also be applied to cast molding and compression molding. Organosilicon compounds, for example, those in which the terminal or side chain R in the formula [1] above represents a methyl group, a phenyl group, and some of these R are replaced with a hydrogen group or a hydroxyl group, or an amino group or an epoxy group. Specifically, in hydrogen group-modified silicones, silanol-modified silicones, amino-modified silicones, epoxy-modified silicones, etc., hydrogen groups, or reactive groups such as hydroxyl groups, amino groups, and epoxy groups are unsaturated. Moisture resistance can be improved by reacting with the vinyl groups of polyester resin. Next, the present invention will be specifically explained using Examples and Comparative Examples. Examples 1 to 5 Unsaturated polyester resin obtained by reacting 1 mol of isophthalic acid, 1 mol of fumaric acid, and 2.2 mol of propylene glycol was blended, mixed, and kneaded according to the first mixing bale to encapsulate electronic components. A molding material for stopping was obtained.

【表】 上記のようにして実施例1及び2と実施例4及
び5で得られた成形材料をトランスフアー成形材
を用いて金型温度145℃、成形圧力40Kg/cm2、硬
化時間2分の条件で成形品を成形し、又実施例3
で得られた成形材料については注型成形し150℃
で30分間硬化させて成形品を得た。 比較例 実施例1から有機シリコン化合物を除去したも
のを実施例1と同様に処理して成形品を得た。 実施例1乃至5及び比較例の成形品の表面漏れ
電流試験及び表面撥水試験をおこなつた結果は第
2表に示すように本発明の電子部品封止用成形材
料から得られた成形品の表面漏れ電流は少なく、
又表面撥水性がよく本発明による電子部品封止用
成形材料の優れていることを確認した。
[Table] The molding materials obtained in Examples 1 and 2 and Examples 4 and 5 as described above were molded using a transfer molding material at a mold temperature of 145°C, a molding pressure of 40 Kg/cm 2 , and a curing time of 2 minutes. A molded product was molded under the conditions of Example 3.
The molding material obtained is cast and molded at 150℃.
The molded product was obtained by curing for 30 minutes. Comparative Example A molded article was obtained from Example 1 with the organosilicon compound removed and treated in the same manner as in Example 1. The results of the surface leakage current test and surface water repellency test of the molded products of Examples 1 to 5 and Comparative Examples are as shown in Table 2. The surface leakage current of
It was also confirmed that the molding material for encapsulating electronic components according to the present invention has good surface water repellency.

【表】【table】

Claims (1)

【特許請求の範囲】 1 不飽和ポリエステル樹脂、架橋剤、充填剤、
添加剤からなる不飽和ポリエステル樹脂成形材料
に式〔1〕で表される有機シリコン化合物を添加
してなることを特徴とする電子部品封止用成形材
料。 (式〔1〕においてRはメチル基、フエニル基を
示す。) 2 有機シリコン化合物の添加量が0.01〜3重量
%であることを特徴とする特許請求の範囲第1項
記載の電子部品封止用成形材料。 3 式〔1〕で表される有機シリコン化合物の末
端のRまたは、側鎖のRの一部が水酸基、アミノ
基、エポキシ基で変性されたものであることを特
徴とする特許請求の範囲第1項または、第2項記
載の電子部品封止用成形材料。
[Claims] 1. Unsaturated polyester resin, crosslinking agent, filler,
A molding material for encapsulating electronic components, which is made by adding an organic silicon compound represented by formula [1] to an unsaturated polyester resin molding material comprising an additive. (In formula [1], R represents a methyl group or a phenyl group.) 2. Electronic component encapsulation according to claim 1, characterized in that the amount of the organic silicon compound added is 0.01 to 3% by weight. molding material. 3. Claim No. 3, characterized in that the terminal R or side chain R of the organosilicon compound represented by formula [1] is partially modified with a hydroxyl group, an amino group, or an epoxy group. The molding material for encapsulating electronic components according to item 1 or 2.
JP56069652A 1981-05-08 1981-05-08 DENSHIBUHINFUSHOSEIKEIZAIRYO Expired - Lifetime JPH0234182B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56069652A JPH0234182B2 (en) 1981-05-08 1981-05-08 DENSHIBUHINFUSHOSEIKEIZAIRYO

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56069652A JPH0234182B2 (en) 1981-05-08 1981-05-08 DENSHIBUHINFUSHOSEIKEIZAIRYO

Publications (2)

Publication Number Publication Date
JPS57184243A JPS57184243A (en) 1982-11-12
JPH0234182B2 true JPH0234182B2 (en) 1990-08-01

Family

ID=13408980

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56069652A Expired - Lifetime JPH0234182B2 (en) 1981-05-08 1981-05-08 DENSHIBUHINFUSHOSEIKEIZAIRYO

Country Status (1)

Country Link
JP (1) JPH0234182B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4405662A (en) * 1981-11-05 1983-09-20 Shell Oil Company Thermosetting resinous binder compositions and their use as coating materials
JP3827391B2 (en) * 1997-03-04 2006-09-27 昭和高分子株式会社 Resin composition for sealing
JP2013010946A (en) * 2011-05-31 2013-01-17 Toto Ltd Artificial marble molded article

Also Published As

Publication number Publication date
JPS57184243A (en) 1982-11-12

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