JPS60248722A - Casting composition - Google Patents
Casting compositionInfo
- Publication number
- JPS60248722A JPS60248722A JP10521084A JP10521084A JPS60248722A JP S60248722 A JPS60248722 A JP S60248722A JP 10521084 A JP10521084 A JP 10521084A JP 10521084 A JP10521084 A JP 10521084A JP S60248722 A JPS60248722 A JP S60248722A
- Authority
- JP
- Japan
- Prior art keywords
- acrylate
- meth
- casting composition
- emitting diode
- light emitting
- 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
Abstract
Description
【発明の詳細な説明】
〔技術分野〕
本発明は発光ダイオードを注型により樹脂封止する際に
用いられる注型用組成物に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Technical Field] The present invention relates to a casting composition used when resin-sealing a light emitting diode by casting.
一般に発光ダイオードを外部環境から保護するため透明
性を有するエポキシ樹脂と酸無水物系硬化剤とを用いト
ランスファー成形や注型によって樹脂封止することが行
なわれているが硬化時間が数十分乃至数時間必要で且つ
発光ダイオードのリード線の燐青銅が硬化剤の酸、塩基
性物質に侵され緑青を発生させる問題があった。Generally, in order to protect light emitting diodes from the external environment, transparent epoxy resin and acid anhydride curing agents are used to encapsulate the LEDs by transfer molding or casting, but the curing time is several tens of minutes to a few minutes. It takes several hours, and there is a problem that the phosphor bronze of the lead wire of the light emitting diode is attacked by the acid or basic substance of the hardening agent, causing a patina.
本発明の目的とするところは硬化時間が短かく、且つ発
光ダイオードのリード線腐蝕のない発光ダイオード樹脂
封止用の注型用組成物を提供することにある。An object of the present invention is to provide a casting composition for resin-sealing a light-emitting diode, which has a short curing time and is free from corrosion of the lead wires of the light-emitting diode.
本発明はラジカル重合可能な不飽和二重結合を有するオ
リゴマー及び化ツマ−と光重合開始剤とを含有すること
を特徴とすみ注型用組成物で、以下本発明の詳細な説明
する。The present invention relates to a fill casting composition characterized by containing an oligomer having a radically polymerizable unsaturated double bond, a polymer, and a photopolymerization initiator, and the present invention will be described in detail below.
本発明に用いるラジカル重合可能な不飽和二重結合を有
するオリゴマーはエポキシ樹脂、ウレタン樹脂のアクリ
レートやメタクリレート及び不飽和ポリエステV樹脂等
でラジカル重合可能な不飽和二重結合を有するオリゴマ
ーであればよく特に限定するものではないが好ましくは
透明性を有するものであふことか望ましい。化ツマ−と
してはメタVメタクリレート、ブチ々メタクリレート、
ヒドロギシエチ〃メタクリレート、エチレングリコール
シ(メタ)アクリレート、ポリエチレングリコールジ(
メタ)アクリレート、トリメチロ−Vプロパントリ(メ
タ)アクリレート、ペンタエリスリトールトリ(メタ)
アクリレート、スチレン、ビニルトVエン等が用いられ
ふか好捷しくは透明性を有するものであることが2甘し
い。光重合開始剤としてはペンゾインメチルエーテM、
ペンゾインエチVエーテV、ベンゾインイソプロピルエ
ーテル、ベンジン、ベンゾフェノン、アセトフェノン、
アントラキノン、2−エチルγントラキノン、ベンジル
メチルケタ−M、ヒドロキシシクロヘキシVフエ二Mケ
トン、ジェトキシアセトフェノン等が用いられ特に限定
するものではな、いが好ましくは硬化後に黄変等の新合
をおこさないものを選ぶことが望ましくこの点、ヒドロ
キシシクロへキシルフエニVケトン、ジェトキシアセト
フェノンは変色が少ないので好ましい光重合開始剤であ
み。光重合開始剤の添加量は組成物全体に対し0.5〜
5重量係最多下単に係と記す)添加することが望ましい
ことである。なおこれらの成分を含有する注型用組成剤
はカップリング剤、顔料、充填剤を含有して構成される
ものを除外するものではなく適宜必要に応じて添加して
使用に供される。The oligomer having an unsaturated double bond that can be radically polymerized to be used in the present invention may be an oligomer that has an unsaturated double bond that can be radically polymerized with epoxy resin, acrylate or methacrylate of urethane resin, unsaturated polyester V resin, etc. Although not particularly limited, it is preferable that the material be transparent. As a chemical agent, Meta V methacrylate, butitoshi methacrylate,
Hydroxythiol methacrylate, ethylene glycol di(meth)acrylate, polyethylene glycol di(
meth)acrylate, trimethylo-Vpropane tri(meth)acrylate, pentaerythritol tri(meth)
Acrylate, styrene, vinylene, etc. are used, and preferably transparent ones are used. As a photopolymerization initiator, penzoin methyl ether M,
Penzoin ethyl ether V, benzoin isopropyl ether, benzine, benzophenone, acetophenone,
Anthraquinone, 2-ethyl γ-anthraquinone, benzyl methyl ket-M, hydroxycyclohexy V-pheniM ketone, jetoxyacetophenone, etc. are used, but are not particularly limited, but preferably do not cause new synthesis such as yellowing after curing. In this respect, it is desirable to choose a photopolymerization initiator that does not cause any discoloration, and hydroxycyclohexylphenylated ketone and jetoxyacetophenone are preferred photopolymerization initiators because they cause little discoloration. The amount of photopolymerization initiator added is 0.5 to 0.5 to the total composition.
It is desirable to add 5% by weight (simply written as %). Note that casting compositions containing these components do not exclude those containing coupling agents, pigments, and fillers, and may be added as appropriate and used.
以下、この発明の効果を具体的に裏付ける実施例を挙げ
る。Examples that specifically support the effects of this invention will be given below.
実施例
エポキシアクリレート樹脂(大日末インキ化学工業株式
会社製、商品名U E −8200) 50重量部(以
下単に部と記す)に対しアクリレートモノマー(大阪有
機化学株式会社製、商品名ビスコ−) 190)50部
、光重合開始剤(チパガイギー製、商品名イMガキュア
ー184 ) 1部を加えた注型用組成物を、発光ダイ
オードをセットした透明なポリメチVペンテン樹脂製金
型内に注型後、80W/Cm の高圧水銀灯で紫外線照
射したところ照射線量ago m j /cd、20秒
間で硬化し発光ダイオードのリード線腐蝕は全く見られ
なかった。Example: Acrylate monomer (manufactured by Osaka Organic Chemical Co., Ltd., trade name Visco-) to 50 parts by weight (hereinafter simply referred to as parts) of epoxy acrylate resin (manufactured by Dainichisue Ink Chemical Co., Ltd., trade name UE-8200) 190) A casting composition containing 50 parts of a photopolymerization initiator (manufactured by Chipa Geigy, trade name: IM Gacure 184) was poured into a transparent polymethyV-pentene resin mold in which a light emitting diode was set. Thereafter, when it was irradiated with ultraviolet rays using a high-pressure mercury lamp of 80 W/Cm 2 , it was cured in 20 seconds at an irradiation dose of ago m j /cd, and no corrosion of the lead wires of the light emitting diode was observed at all.
従来例
エポキシ樹脂(シエM化学株式会社製、商品名工ピコ−
) 82B ) 100部に対し無水メチ々ハイミック
酸80部を加えた注型用組成物を発光ダイオードをセッ
トしたシリコン樹脂製金型内に注型後、160℃で5時
間加熱して硬化させたが発光ダイオードのリード線に緑
青が発生していた。Conventional example epoxy resin (manufactured by CieM Chemical Co., Ltd., product name Ko Pico)
) 82B) A casting composition prepared by adding 80 parts of methihymic acid anhydride to 100 parts was poured into a silicone resin mold in which a light emitting diode was set, and then heated at 160° C. for 5 hours to cure it. However, a patina appeared on the lead wire of the light emitting diode.
[発明の効果]
実施例、従来例に掲げるように本発明の注型用組成物の
硬化時間は短かく且つ発光ダイオードのリード線閥蝕が
なく本発明の優れていることを確認した。[Effects of the Invention] As shown in Examples and Conventional Examples, the curing time of the casting composition of the present invention was short and there was no corrosion of the lead wires of the light emitting diode, confirming the superiority of the present invention.
特許出願人 松下電工株式会社 代理人弁理士 竹元敏丸(ほか2名)patent applicant Matsushita Electric Works Co., Ltd. Representative Patent Attorney Toshimaru Takemoto (and 2 others)
Claims (1)
リゴマー及び化ツマ−と光重合開始剤とを含有すること
を特徴とする注型用組成物。 (2> オリゴマー及び化ツマ−が透明性を有している
ことを特徴とする特許請求の範囲第1項記載の注型用組
成物。(1) A casting composition characterized by containing an oligomer and polymer having a radically polymerizable unsaturated double bond and a photopolymerization initiator. (2> The casting composition according to claim 1, wherein the oligomer and the polymer have transparency.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10521084A JPS60248722A (en) | 1984-05-24 | 1984-05-24 | Casting composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10521084A JPS60248722A (en) | 1984-05-24 | 1984-05-24 | Casting composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS60248722A true JPS60248722A (en) | 1985-12-09 |
Family
ID=14401299
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10521084A Pending JPS60248722A (en) | 1984-05-24 | 1984-05-24 | Casting composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60248722A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0384729A3 (en) * | 1989-02-23 | 1992-03-18 | U C B, S.A. | Radiation curable acrylate polyesters |
-
1984
- 1984-05-24 JP JP10521084A patent/JPS60248722A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0384729A3 (en) * | 1989-02-23 | 1992-03-18 | U C B, S.A. | Radiation curable acrylate polyesters |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA1076296A (en) | Photo-polymerizable dental restorative and tooth coating composition comprising an oligomeric resin, an acrylate monomer, an organic peroxide and a photosensitizer | |
US4267133A (en) | Manufacture of denture base | |
JPH05202146A (en) | Photosetting resin composition | |
JPH05507729A (en) | Use of compositions based on organically modified silicic acid polycondensates for coating teeth and dental prostheses | |
ES520272A0 (en) | PROCEDURE FOR OBTAINING A PHOTOPOLYMERIZABLE COMPOSITION CONTAINING AT LEAST ONE ETHYLINICALLY UNSATURATED POLYMERIZABLE MONOMER. | |
US4112146A (en) | Polyester resin compositions which are photocurable in the presence of oxygen and an organic hydrazone polymerization initiator | |
WO1985001947A1 (en) | Photocurable (meth)acrylate and cationic monomers or prepolymers | |
JPH09194540A (en) | Resin composition for forming optical three-dimensional article | |
EP0233081B1 (en) | Active energy ray-curable composition | |
JPS59138203A (en) | Photopolymerizable composition and photopolymerization | |
Lima et al. | Mechanical properties of experimental resin cements containing different photoinitiators and co-initiators | |
JPS60248722A (en) | Casting composition | |
JPH06505201A (en) | Three-dimensional modeling method using a composition that can reduce deformation | |
JPH09107128A (en) | Resin-encapsulated high-brightness light emitting diode and its manufacturing method | |
JPS60215008A (en) | High-energy ray-curable resin composition | |
JPS6314002B2 (en) | ||
JPS58103519A (en) | Curable resin composition | |
JPS6121490B2 (en) | ||
KR100845089B1 (en) | Encapsulation method of light emitting diode | |
JPS58219781A (en) | Sealing method for light emitting diode element | |
JPH0442836B2 (en) | ||
JP7160289B2 (en) | dental curable composition | |
US3664937A (en) | Photosensitizing molding and coating compositions with benzoin-silyl-esters | |
JPH05255454A (en) | Optical part | |
NZ208673A (en) | Photopolymerisation using alpha-halogenated benzene derivatives as photoinitiators |