JPH11279458A - Moisture preventing electrically insulating coating material and electric/electronic part using the same - Google Patents

Moisture preventing electrically insulating coating material and electric/electronic part using the same

Info

Publication number
JPH11279458A
JPH11279458A JP7905598A JP7905598A JPH11279458A JP H11279458 A JPH11279458 A JP H11279458A JP 7905598 A JP7905598 A JP 7905598A JP 7905598 A JP7905598 A JP 7905598A JP H11279458 A JPH11279458 A JP H11279458A
Authority
JP
Japan
Prior art keywords
weight
parts
moisture
coating material
electrically insulating
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
JP7905598A
Other languages
Japanese (ja)
Inventor
Masakatsu Obara
正且 小原
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.)
Showa Denko Materials Co Ltd
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 JP7905598A priority Critical patent/JPH11279458A/en
Publication of JPH11279458A publication Critical patent/JPH11279458A/en
Pending legal-status Critical Current

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  • Paints Or Removers (AREA)
  • Macromonomer-Based Addition Polymer (AREA)
  • Organic Insulating Materials (AREA)

Abstract

PROBLEM TO BE SOLVED: To obtain a moisture preventing electrically insulating coating material excellent in flexibility and moisture resistance and capable of being finished in a short time, and to provide electric/electronic parts subjected to a moisture preventing electrically insulating treatment by using the coating material. SOLUTION: This coating material comprises; (a) 100 pts.wt. of resin obtained by reacting a hydroxy group-containing polyisoprene having a hydrogeneration ratio of >=90% with a polyisocyanate and then reacting it with a hydroxy group- containing polymerizable unsaturated monomer, (b) 0.5 to 20 pts.wt. of silane- based coupling agent, (c) 0.01 to 10 pts.wt. of photopolymerization initiator and (d) 10 to 300 pts.wt. of solvent. The other objective electric/electronic parts are subjected to a moisture preventing electrically insulating treatment by busing the coating material.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、防湿絶縁塗料及び
この防湿絶縁塗料を用いて防湿絶縁処理された電気電子
部品に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a moisture-proof insulating paint and an electric and electronic component subjected to a moisture-proof insulating treatment using the moisture-proof insulating paint.

【0002】[0002]

【従来の技術】従来、実装回路板及びハイブリッドIC
には、ガラスエポキシ、アルミナセラミック等に回路が
印刷されてマイコン、抵抗体、コンデンサー等の各種電
子部品が搭載されており、それらの部品間を絶縁し、ま
た湿気、ほこり等から保護するためにアクリル樹脂、シ
リコーン樹脂、エポキシ樹脂等の塗料による保護コーテ
イング処理が広く行われている。このような実装回路板
及びハイブリッドICは、過酷な環境下、特に自動車、
洗濯機等に搭載され高湿度下で使用される機器に多く使
用されている。
2. Description of the Related Art Conventionally, mounted circuit boards and hybrid ICs
The circuit is printed on glass epoxy, alumina ceramic, etc., and various electronic parts such as microcomputer, resistor, capacitor, etc. are mounted, to insulate those parts and to protect from moisture, dust, etc. Protective coating treatment with a paint such as an acrylic resin, a silicone resin, or an epoxy resin is widely performed. Such a mounted circuit board and a hybrid IC are used in a severe environment, particularly in an automobile,
It is often used in equipment that is installed in washing machines and used under high humidity.

【0003】しかしながら、前記塗料は加熱硬化性であ
るため、塗料を完全に硬化させて絶縁効果を得るために
は高温度処理、または長時間処理が必要であった。一
方、短時間処理、例えぱ、数秒〜数分での硬化が可能な
紫外線硬化性樹脂塗料が開発されているが、まだ充分な
可とう性及び耐湿性を有するものが得られていない。
However, since the paint is heat-curable, a high temperature treatment or a long-time treatment is required to completely cure the paint and obtain an insulating effect. On the other hand, an ultraviolet-curable resin paint capable of being cured in a short time, for example, in a few seconds to a few minutes, has been developed, but one having sufficient flexibility and moisture resistance has not yet been obtained.

【0004】[0004]

【発明が解決しようとする課題】本発明は、前記従来技
術の問題点を解消し、短時間処理が可能で、可とう性及
び耐湿性に優れた防湿絶縁塗料及びこの防湿絶縁塗料を
用いて防湿絶縁処理された電気電子部品を提供すること
を目的とする。
DISCLOSURE OF THE INVENTION The present invention solves the above-mentioned problems of the prior art, and can be processed in a short time, and is excellent in flexibility and moisture resistance. It is an object of the present invention to provide an electric and electronic component that has been subjected to moisture-proof insulation treatment.

【0005】[0005]

【課題を解決するための手段】本発明は、(a)水素添
加率が90%以上である水酸基含有ポリイソプレンをポ
リイソシアネートと反応させ、その後、水酸基を有する
重合性不飽和単量体を反応させて得られる樹脂100重
量部、(b)シラン系カップリング剤を0.5〜20重
量部、(c)光重合開始剤を0.01〜10重量部、
(d)溶剤を10〜300重量部を含有してなる防湿絶
縁塗料及びこの防湿絶縁塗料を用いて防湿絶縁処理され
た電気電子部品に関する。本発明は、また、この防湿絶
縁塗料を用いて防湿絶縁処理された電気電子部品に関す
る。
According to the present invention, (a) a hydroxyl group-containing polyisoprene having a hydrogenation rate of 90% or more is reacted with a polyisocyanate, and then a polymerizable unsaturated monomer having a hydroxyl group is reacted. 100 parts by weight of a resin obtained by the reaction, (b) 0.5 to 20 parts by weight of a silane coupling agent, (c) 0.01 to 10 parts by weight of a photopolymerization initiator,
(D) The present invention relates to a moisture-proof insulating paint containing 10 to 300 parts by weight of a solvent, and an electric and electronic component subjected to moisture-proof insulation treatment using the moisture-proof insulating paint. The present invention also relates to electrical and electronic components that have been subjected to moisture-proof insulation treatment using the moisture-proof insulation paint.

【0006】[0006]

【発明の実施の形態】本発明の防湿絶縁塗料において、
(a)成分の樹脂の数平均分子量は500〜10,00
0のものが好ましく、1,000〜5,000のものが
より好ましい。数平均分子量が500未満では造膜性が
悪くなり、10,000を越えると塗料の粘度が高くな
り、作業性に劣る。
BEST MODE FOR CARRYING OUT THE INVENTION In the moisture-proof insulating paint of the present invention,
The number average molecular weight of the resin (a) is from 500 to 10,000.
0 is preferable, and 1,000 to 5,000 is more preferable. When the number average molecular weight is less than 500, the film-forming property is deteriorated, and when it exceeds 10,000, the viscosity of the coating material becomes high and the workability is poor.

【0007】(a)成分の樹脂の原料である水素添加率
が90%以上である水酸基含有ポリイソプレンは、分子
中または分子末端に水酸基を有し、水酸基含有量が0.
6〜1.5meq/g、数平均分子量が約500〜約10,
000のものが好ましく、約1,000〜約5,000
のもが特に好ましい。この水酸基含有ポリイソプレンの
水素添加率が90%以上を有するもので、市販品として
は出光石油化学(株)製の商品名エポールが挙げられる。
また、水素添加率は90%以上のものが好ましく、95
%以上のものがより好ましい。水素添加率が90%未満
では得られる塗膜の熱劣化後の可とう性が低下し、耐熱
性に劣る。尚、本発明において数平均分子量は、蒸気圧
浸透圧法により測定したものである。また、水素添加率
の度合は、別の釈度としてヨウ素価ではかることがで
き、前記水酸基含有ポリイソプレンのヨウ素価は、40
以下が好ましく、特に20以下が好ましい。
The hydroxyl group-containing polyisoprene having a hydrogenation rate of 90% or more, which is a raw material of the resin as the component (a), has a hydroxyl group in a molecule or at a molecular terminal and has a hydroxyl group content of 0.1%.
6 to 1.5 meq / g, number average molecular weight of about 500 to about 10,
000 is preferable, and about 1,000 to about 5,000
Are particularly preferred. The hydroxyl group-containing polyisoprene has a hydrogenation rate of 90% or more, and commercially available products include Epole manufactured by Idemitsu Petrochemical Co., Ltd.
The hydrogenation rate is preferably 90% or more.
% Or more is more preferable. If the hydrogenation ratio is less than 90%, the flexibility of the obtained coating film after thermal deterioration is reduced, and the heat resistance is poor. In the present invention, the number average molecular weight is measured by a vapor pressure osmometry. The degree of the hydrogenation rate can be measured by an iodine value as another degree. The iodine value of the hydroxyl group-containing polyisoprene is 40%.
The following is preferable, and especially 20 or less is preferable.

【0008】さらに、(a)成分の樹脂の原料であるポ
リイソシアネートは、前記の水酸基含有ポリイソプレン
の水酸基及び水酸基を有する重合性不飽和単量体と反応
して、ポリマーを形成するために使用されるものであ
り、例えぱ、トリレンジイソシアネート、ジフェニルメ
タンジイソシアネート、ナフタレンジイソシアネート、
キシリレンジイソシアネート、ヘキサメチレンジイソシ
アネート等のジイソシアネート化合物、トリフエニルメ
タントリイソシアネート等のトリイソシアネート化合物
などのポリイソシアネート化合物またはこれらのポリイ
ソシアネート化合物のイソシアネート基をフエノール
類、イミド類、オキシム類、アルコール類等でブロック
化した化合物、カルボジイミド変性ジフェニルメタンジ
イソシアネート等の前記ポリイソシアネートから誘導さ
れる末端イソシアネート基を有するプレポリマーなどが
挙げられ、これらを単独でまたは2種類以上を組み合わ
せて使用することができる。
Further, the polyisocyanate which is a raw material of the resin of the component (a) is used for forming a polymer by reacting with the hydroxyl group of the hydroxyl group-containing polyisoprene and the polymerizable unsaturated monomer having a hydroxyl group. For example, tolylene diisocyanate, diphenylmethane diisocyanate, naphthalene diisocyanate,
Xylylene diisocyanate, diisocyanate compound such as hexamethylene diisocyanate, polyisocyanate compound such as triisocyanate compound such as triphenylmethane triisocyanate, or the isocyanate group of these polyisocyanate compounds with phenols, imides, oximes, alcohols, etc. Examples include blocked compounds, prepolymers having terminal isocyanate groups derived from the above-mentioned polyisocyanates such as carbodiimide-modified diphenylmethane diisocyanate, and these can be used alone or in combination of two or more.

【0009】水酸基を有する重合性不飽和単量体として
は、炭素数が1〜10のヒドロキシアルキル基、炭素数
が1〜10のポリ(アルキレンオキシ)アルキル基を有
するアクリレート又はメタクリレート等があり、具体的
には、ヒドロキシエチルアクリレート、ヒドロキシプロ
ピルアクリレート、ヒドロキシブチルアクリレート、ヒ
ドロキシヘキシルアクリレート、ヒドロキシオクチルル
アクリレート、ジエチレングリコールモノアクリレー
ト、ジプロピレングリコールモノアクリレート等の水酸
基を有するアクリル酸エステル、ヒドロキシエチルメタ
クリレート、ヒドロキシプロピルメタクリレート、ヒド
ロキシブチルメタクリレート、ヒドロキシヘキシルメタ
クリレート、ヒドロキシオクチルルメタクリレート、ジ
エチレングリコールモノメタクリレート、ジプロピレン
グリコールモノメタクリレート等の水酸基を有するメタ
クリル酸エステル等がある。
Examples of the polymerizable unsaturated monomer having a hydroxyl group include an acrylate or methacrylate having a hydroxyalkyl group having 1 to 10 carbon atoms and a poly (alkyleneoxy) alkyl group having 1 to 10 carbon atoms. Specifically, acrylates having a hydroxyl group such as hydroxyethyl acrylate, hydroxypropyl acrylate, hydroxybutyl acrylate, hydroxyhexyl acrylate, hydroxyoctyl acrylate, diethylene glycol monoacrylate, dipropylene glycol monoacrylate, hydroxyethyl methacrylate, hydroxypropyl Methacrylate, hydroxybutyl methacrylate, hydroxyhexyl methacrylate, hydroxyoctyl methacrylate, diethylene glycol Bruno methacrylate, methacrylic acid ester having a hydroxyl group such as dipropylene glycol monomethacrylate.

【0010】(a)成分の樹脂を合成する方法として
は、通常の水酸基とイソシアネート基を反応させる方法
でよく、特に制限されるものではない。合成方法の一例
としては、最初に水酸基含有ポリイソプレンとポリイソ
シアネートを配合して反応させ、分子末端にイソシアネ
ート基を有するプレポリマーを得た後、次に水酸基を有
する重合性不飽和単量体を反応させる。
The method of synthesizing the resin as the component (a) may be a method of reacting an ordinary hydroxyl group with an isocyanate group, and is not particularly limited. As an example of the synthesis method, first, a hydroxyl group-containing polyisoprene and a polyisocyanate are blended and reacted to obtain a prepolymer having an isocyanate group at a molecular terminal, and then a polymerizable unsaturated monomer having a hydroxyl group is added. Let react.

【0011】水酸基含有ポリイソプレンの水酸基とポリ
イソシアネートのイソシアネート基の比率は、水酸基1
当量に対して、イソシアネート基が1.4〜2.4当量
とすることが好ましく、特に、水酸基1当量に対して、
イソシアネート基が1.6〜2.2当量とすることが好
ましい。
The ratio of the hydroxyl groups of the hydroxyl group-containing polyisoprene to the isocyanate groups of the polyisocyanate is 1 hydroxyl group
It is preferable that the isocyanate group is 1.4 to 2.4 equivalents with respect to the equivalent weight.
It is preferable that the isocyanate group is 1.6 to 2.2 equivalents.

【0012】また、水酸基含有ポリイソプレンの水酸基
と水酸基を有する重合性不飽和単量体の水酸基の総量と
ポリイソシアネートのイソシアネート基の比率は、水酸
基1当量に対して、イソシアネート基が0.7〜1.2
当量とすることが好ましく、特に、水酸基1当量に対し
て、イソシアネート基が0.8〜1.1当量とすること
が好ましい。
The ratio of the total number of hydroxyl groups of the hydroxyl group-containing polyisoprene and the hydroxyl group-containing polymerizable unsaturated monomer to the isocyanate group of the polyisocyanate is 0.7 to 0.7% per equivalent of hydroxyl group. 1.2
It is preferable that the isocyanate group is equivalent to 0.8 to 1.1 equivalent to 1 equivalent of the hydroxyl group.

【0013】本発明における(b)成分のシラン系カッ
プリング剤としては、一般式(I)
The silane coupling agent of the component (b) in the present invention is represented by the general formula (I)

【化1】 (ただし、式中、Zは、ビニル基、炭素数3〜10アク
リロイルオキシアルキル基、炭素数4〜11メタクリロ
イルオキシアルキル基等の反応性二重結合を有する基、
Rは炭素数1〜6のアルキル基又は炭素数6〜22の芳
香族基を示す)で表される化合物が好ましい。具体的に
は、γ−メタクリロキシプロピルトリメトキシシラン、
γ−メタクリロキシプロピルトリエトキシシラン、γ−
アクリロキシプロピルトリメトキシシラン、ビニルトリ
メトキシシラン、ビニルトリエトキシシラン等が挙げら
れ、これらを単独でまたは2種類以上を組み合わせて使
用することができる。
Embedded image (Wherein, Z is a group having a reactive double bond such as a vinyl group, a C3-10 acryloyloxyalkyl group, a C4-11 methacryloyloxyalkyl group,
R represents an alkyl group having 1 to 6 carbon atoms or an aromatic group having 6 to 22 carbon atoms). Specifically, γ-methacryloxypropyltrimethoxysilane,
γ-methacryloxypropyltriethoxysilane, γ-
Acryloxypropyltrimethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane and the like can be mentioned, and these can be used alone or in combination of two or more.

【0014】(b)成分の配合割合は、前記(a)成分
100重量部に対して0.5〜20重量部とすることが
好ましく、0.7〜15重量部とすることがより好まし
く、1〜10重量部とすることが特に好ましい。0.5
重量部未満では得られる塗膜の耐湿性が悪くなり、20
重量部を越えると可とう性が低下する。
The mixing ratio of the component (b) is preferably 0.5 to 20 parts by weight, more preferably 0.7 to 15 parts by weight, based on 100 parts by weight of the component (a). It is particularly preferred that the amount be 1 to 10 parts by weight. 0.5
If the amount is less than 10 parts by weight, the resulting coating film has poor moisture resistance,
Exceeding the parts by weight reduces the flexibility.

【0015】本発明における(c)成分の光重合開始剤
としては、ベンゾイン、ベンジルジメチルケタール、ベ
ンゾインエチルエーテル等のベンゾインエーテル類、エ
トキシアセトフェノン、ヒドロキシアセトフェノン等の
アセトフェノン構造を有する分子内結合解裂型の光重合
開始剤、ベンゾインチオエーテル類、ベンゾフエノン、
アセトフエノン、2一エチルアントラキノン、ミヒラー
ケトン、塩化デシルノチオキサントン、イソブチルチオ
キサントン等のチオキサントン構造を有する分子内水素
引き抜き型光重合開始剤などが挙げられ、これらを単独
でまたは2種類以上を組み合わせて使用することができ
る。(c)成分の配合割合は、前記(a)成分100重
量部に対して0.01〜10重量部とすることが好まし
く、0.05〜8重量部とすることがより好ましく、
0.1〜5重量部とすることが特に好ましい。0.01
重量部未溝では光照射による硬化遠度が遅くなり、10
重量部を越えると造膜し難くなる。
As the photopolymerization initiator of the component (c) in the present invention, benzoin ethers such as benzoin, benzyldimethyl ketal and benzoin ethyl ether; Photopolymerization initiator, benzoin thioethers, benzophenone,
Intramolecular hydrogen abstraction type photopolymerization initiator having a thioxanthone structure such as acetophenone, 21-ethylanthraquinone, Michler's ketone, decylnothioxanthone chloride, isobutylthioxanthone, etc., and these may be used alone or in combination of two or more. Can be. The compounding ratio of the component (c) is preferably 0.01 to 10 parts by weight, more preferably 0.05 to 8 parts by weight, based on 100 parts by weight of the component (a).
It is particularly preferred that the amount be 0.1 to 5 parts by weight. 0.01
If the groove is not grooved, the curing distance by light irradiation becomes slow, and
Exceeding parts by weight makes film formation difficult.

【0016】本発明における(d)成分の溶剤として
は、トルエン、キシレン等の芳香族系溶剤が樹脂の溶解
性の点から好ましい。(d)成分の配合割合は、前記
(a)成分100重量部に対して10〜300重量部と
することが好ましく、50〜250重量部とすることが
より好ましく、75〜200重量部とすることが特に好
ましい。1O重量部未溝では粘度が高く、作業性が悪く
なり、300重量部を越えると塗膜が薄くなり耐湿性が
低下する可能性がある。
As the solvent of the component (d) in the present invention, aromatic solvents such as toluene and xylene are preferable from the viewpoint of solubility of the resin. The mixing ratio of the component (d) is preferably 10 to 300 parts by weight, more preferably 50 to 250 parts by weight, and more preferably 75 to 200 parts by weight based on 100 parts by weight of the component (a). Is particularly preferred. If the groove is not 10 weight parts, the viscosity is high and the workability is deteriorated. If it exceeds 300 weight parts, the coating film becomes thin and the moisture resistance may be reduced.

【0017】本発明の防湿絶縁塗料は、前記(a)、
(b)、(c)及び(d)成分の所定量を配合し、撹拌
溶解することによって得られる。この塗料を塗装する方
法としては、一般に知られている浸漬法、スプレー法、
ハケ塗り法等が適用され、塗布後の塗膜の硬化は紫外線
硬化によって行われる。
The moisture-proof insulating paint of the present invention is characterized in that
It is obtained by mixing predetermined amounts of the components (b), (c) and (d) and dissolving with stirring. As a method of applying this paint, generally known dipping method, spray method,
A brush coating method or the like is applied, and the coating film after application is cured by ultraviolet curing.

【0018】本発明の防湿絶縁塗料は、必要に応じてス
チレン、ビニルトルエン等の架橋性単量体、ベンゾイン
パーオキサイド、メチルエチルケトンパーオキサイド等
のラジカル重合開始剤、鉄、コバルト、マンガン等のナ
フテン酸塩、オクテン酸塩等の硬化促進剤、更に、ハイ
ドロキノン、パラターシャリーブチルカテコール等の重
合禁止剤等を添加することができる。
The moisture-proof insulating coating material of the present invention may contain, if necessary, a crosslinkable monomer such as styrene and vinyl toluene, a radical polymerization initiator such as benzoin peroxide and methyl ethyl ketone peroxide, and a naphthenic acid such as iron, cobalt and manganese. Hardening accelerators such as salts and octenoates, and polymerization inhibitors such as hydroquinone and p-tert-butylcatechol can be added.

【0019】[0019]

【実施例】次に、本発明を実施例により説明するが、本
発明はこれらに制限されるものではない。 〔樹脂Aの合成〕1リットル四つロフラスコにエポール
(水酸基含有ポリイソプレン水素化物:数平均分子量
2,500、水酸基含量0.91meq/g、水素添加率9
7%、ヨウ素価12、出光石油化学(株)製)330重量
部とジフェニルメタンジイソシアネート90重量部を加
え、窒素雰囲気下で撹拌し、80℃で2時間反応させ
た。次に、ヒドロキシエチルアクリレート36重量部を
1時間で滴下しながら加え、更に2時間反応させ樹脂A
(数平均分子量:3,500、水素添加率:95%)を
得た。
Next, the present invention will be described with reference to examples, but the present invention is not limited to these examples. [Synthesis of Resin A] Epol (hydroxyl-containing polyisoprene hydride: number average molecular weight: 2,500, hydroxyl group content: 0.91 meq / g, hydrogenation rate: 9)
330 parts by weight (7%, iodine value: 12, Idemitsu Petrochemical Co., Ltd.) and 90 parts by weight of diphenylmethane diisocyanate were added, and the mixture was stirred under a nitrogen atmosphere and reacted at 80 ° C. for 2 hours. Next, 36 parts by weight of hydroxyethyl acrylate was added dropwise over 1 hour, and the mixture was reacted for another 2 hours to obtain resin A.
(Number average molecular weight: 3,500, hydrogenation rate: 95%).

【0020】実施例1 樹脂A100重量部、γ−メタクリロキシプロピルトリ
メトキシシラン4重量部、ベンジルジメチルケタール2
重量部及びキシレン150重量部を混合撹拌し、塗料A
を得た。
Example 1 100 parts by weight of resin A, 4 parts by weight of γ-methacryloxypropyltrimethoxysilane, benzyl dimethyl ketal 2
Parts by weight and 150 parts by weight of xylene were mixed and stirred.
I got

【0021】実施例2 実施例1のγ−メタクリロキシプロピルトリメトキシシ
ランをビニルトリエトキシシラン4重量部を用いた以外
は実施例1と同様にして塗料Bを得た。
Example 2 A coating material B was obtained in the same manner as in Example 1 except that 4 parts by weight of vinyltriethoxysilane was used instead of γ-methacryloxypropyltrimethoxysilane.

【0022】比較例1 実施例1の樹脂AのかわりにTE−2000(日本曹達
(株)製、末端水酸基含有1,2−ポリブタジエンとトリ
レンジイソシアネートの反応物にヒドロキシエチルアク
リレートを反応させて得られた樹脂、数平均分子量1
2,000)100重量部を用いた以外は実施例1と同
様にして塗料Cを得た。
Comparative Example 1 TE-2000 (Nippon Soda) instead of Resin A of Example 1
Co., Ltd., a resin obtained by reacting a reaction product of 1,2-polybutadiene having a terminal hydroxyl group with tolylene diisocyanate with hydroxyethyl acrylate, number average molecular weight 1
Coating C was obtained in the same manner as in Example 1 except that 100 parts by weight of (2,000) was used.

【0023】上記実施例及び比較例で得た塗料A〜Cを
アルミナセラミック基板の櫛形電極(電極間隔0.3
m、電極Ag−Pb製)に、浸漬法により塗布し、ウシ
オ電機社製の照射能力が50W/cmの水銀ランプで照射距
離10cmから120秒間紫外線照射を行い、耐湿性試験
用試験片を作製し、耐湿性を試験した。また、JlSC
2103に準じて屈曲性試験用の試験片を作製して上
記の硬化条件で硬化させ、125℃で240時間放置
し、屈曲性を試験した。その結果を、表1に示す。尚、
耐湿性は耐湿性試験用試験片にDC15V印加しながら
60℃、95%RHの恒温恒湿槽に放置し、表1に示す
時間毎に恒温恒湿槽から取り出し、DC50V印加して
絶縁抵抗を測定した。
The coatings A to C obtained in the above Examples and Comparative Examples were applied to a comb-shaped electrode (electrode spacing 0.3) on an alumina ceramic substrate.
m, electrodes made of Ag-Pb) by an immersion method, and irradiated with UV rays from a mercury lamp with an irradiation capacity of 50 W / cm manufactured by Ushio Inc. from an irradiation distance of 10 cm for 120 seconds to prepare a test piece for a moisture resistance test. And tested for moisture resistance. Also, JlSC
A test piece for a flexibility test was prepared according to 2103, cured under the above curing conditions, left at 125 ° C. for 240 hours, and tested for flexibility. Table 1 shows the results. still,
The moisture resistance was measured by applying a DC voltage of 15 V to the test piece for humidity resistance test, leaving the test piece in a thermo-hygrostat at 60 ° C. and 95% RH. It was measured.

【0024】[0024]

【表1】 [Table 1]

【0025】[0025]

【発明の効果】本発明になる防湿絶縁塗料は、可とう性
及び耐湿性に優れるとともに、紫外線硬化性樹脂を使用
しているため短時間処理が可能である。この塗料により
絶縁された電氣電子部品は信頼性が優れる。
The moisture-proof insulating paint according to the present invention has excellent flexibility and moisture resistance, and can be processed in a short time because it uses an ultraviolet curable resin. Electric and electronic components insulated by this paint have excellent reliability.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI // C08F 299/06 C08F 299/06 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 6 Identification symbol FI // C08F 299/06 C08F 299/06

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 (a)水素添加率が90%以上である水
酸基含有ポリイソプレンをポリイソシアネートと反応さ
せ、その後、水酸基を有する重合性不飽和単量体を反応
させて得られる樹脂100重量部、(b)シラン系カッ
プリング剤を0.5〜20重量部、(c)光重合開始剤
を0.01〜10重量部、(d)溶剤を10〜300重
量部を含有してなる防湿絶縁塗料。
(1) 100 parts by weight of a resin obtained by reacting (a) a hydroxyl group-containing polyisoprene having a hydrogenation rate of 90% or more with a polyisocyanate, and then reacting a polymerizable unsaturated monomer having a hydroxyl group. , (B) 0.5 to 20 parts by weight of a silane coupling agent, (c) 0.01 to 10 parts by weight of a photopolymerization initiator, and (d) 10 to 300 parts by weight of a solvent. Insulating paint.
【請求項2】 請求項1記載の防湿絶縁塗料を用いて防
湿絶縁処理された電気電子部品。
2. An electric and electronic component which has been subjected to moisture-proof insulation treatment using the moisture-proof insulation paint according to claim 1.
JP7905598A 1998-03-26 1998-03-26 Moisture preventing electrically insulating coating material and electric/electronic part using the same Pending JPH11279458A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7905598A JPH11279458A (en) 1998-03-26 1998-03-26 Moisture preventing electrically insulating coating material and electric/electronic part using the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7905598A JPH11279458A (en) 1998-03-26 1998-03-26 Moisture preventing electrically insulating coating material and electric/electronic part using the same

Publications (1)

Publication Number Publication Date
JPH11279458A true JPH11279458A (en) 1999-10-12

Family

ID=13679219

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7905598A Pending JPH11279458A (en) 1998-03-26 1998-03-26 Moisture preventing electrically insulating coating material and electric/electronic part using the same

Country Status (1)

Country Link
JP (1) JPH11279458A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6346980B1 (en) * 2017-07-06 2018-06-20 アイカ工業株式会社 Photocurable moisture-proof insulation coating composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6346980B1 (en) * 2017-07-06 2018-06-20 アイカ工業株式会社 Photocurable moisture-proof insulation coating composition
JP2019014806A (en) * 2017-07-06 2019-01-31 アイカ工業株式会社 Photocurable moisture-proof insulation coating agent composition

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