JPH0475676B2 - - Google Patents

Info

Publication number
JPH0475676B2
JPH0475676B2 JP59008057A JP805784A JPH0475676B2 JP H0475676 B2 JPH0475676 B2 JP H0475676B2 JP 59008057 A JP59008057 A JP 59008057A JP 805784 A JP805784 A JP 805784A JP H0475676 B2 JPH0475676 B2 JP H0475676B2
Authority
JP
Japan
Prior art keywords
parts
formula
weight
compound
acrylate
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
JP59008057A
Other languages
Japanese (ja)
Other versions
JPS60152093A (en
Inventor
Ryuzo Hochin
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 Holdings Corp
Original Assignee
Matsushita Electric Industrial 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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP805784A priority Critical patent/JPS60152093A/en
Publication of JPS60152093A publication Critical patent/JPS60152093A/en
Publication of JPH0475676B2 publication Critical patent/JPH0475676B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Electric Connection Of Electric Components To Printed Circuits (AREA)

Description

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

産業上の利用分野 本発明はプリント基板に電子部品を取付ける方
法に関する。 従来例の構成とその問題点 従来からアクリロイル基もしくはメタクリロイ
ル基を有する化合物と光増感剤および熱重合開始
剤からなる硬化性樹脂組成物を介してチツプ抵抗
やチツプコンデンサなどのチツプ部品をプリント
基板に仮固定し、その後半田デイツプが行なわれ
ていたが、半田デイツプのさい積層チツプコンデ
ンサが0.01%ほど脱落するという問題があつた。
さらに最近は、プリント基板の片面にリード付電
子部品を装着し、もう一方の面にチツプ部品を上
記硬化性樹脂組成物を介して装着し、硬化後チツ
プ部品を装着した面を半田デイツプした後、リー
ド線をカツトし、再び半田デイツプを行なつてい
る。このような2回半田デイツプを行なつた場合
積層チツプコンデンサの脱落率は0.3%と大きく、
半田付け後の検査及び修正に極めて多くの時間を
必要とし問題になつている。 発明の目的 本発明は、上記従来の問題を解決するものであ
り、半田付けの信頼性を高めるものである。 発明の構成 化学式
INDUSTRIAL APPLICATION FIELD OF THE INVENTION The present invention relates to a method of attaching electronic components to a printed circuit board. Structure of conventional examples and their problems Conventionally, chip parts such as chip resistors and chip capacitors are connected to printed circuit boards through a curable resin composition consisting of a compound having an acryloyl group or a methacryloyl group, a photosensitizer, and a thermal polymerization initiator. The capacitors were temporarily fixed to the capacitor and then soldered in.However, there was a problem in which about 0.01% of the multilayer chip capacitors fell off during the soldering process.
Furthermore, recently, electronic components with leads are attached to one side of a printed circuit board, chip components are attached to the other side via the above-mentioned curable resin composition, and after curing, the surface on which the chip components are attached is dip-dipped with solder. Then, the lead wires are cut and solder dip is performed again. When soldering is carried out twice like this, the dropout rate of multilayer chip capacitors is as high as 0.3%.
Inspection and correction after soldering require an extremely large amount of time, which has become a problem. OBJECTS OF THE INVENTION The present invention solves the above-mentioned conventional problems and improves the reliability of soldering. Structure of the invention Chemical formula

【式】(XはHまたは CH3)で表わされるアクリレートまたはメタクリ
レートでRが
Acrylate or methacrylate represented by [Formula] (X is H or CH 3 ), where R is

【式】基を有する化合物(A) 0.05〜5重量部と、 化学式[Formula] Compound (A) having a group 0.05 to 5 parts by weight, Chemical formula

【式】(XはHまたは CH3)で表わされるアクリレートまたはメタクリ
レートでRが
Acrylate or methacrylate represented by [Formula] (X is H or CH 3 ), where R is

【式】基を有しない化合物で あつて、エポキシアクリレート化合物を少なくと
も含む化合物(B)100重量部と、光増感剤(C)もしく
は熱重合開始剤(D)0.05〜5重量部とを含む硬化性
樹脂組成物を介してプリント基板の電子部品搭載
部に電子部品を接着し、硬化後半田付けする電子
部品の取付け方法であり、半田付け時の電子部品
の脱落を大幅に削減でき、生産性及び信頼性を高
めることができる。 Rが
[Formula] Contains 100 parts by weight of a compound (B) that does not have a group and contains at least an epoxy acrylate compound, and 0.05 to 5 parts by weight of a photosensitizer (C) or a thermal polymerization initiator (D) This is an electronic component mounting method in which electronic components are bonded to the electronic component mounting area of a printed circuit board via a curable resin composition and soldered after curing. This method significantly reduces the chance of electronic components falling off during soldering, and reduces production costs. performance and reliability can be improved. R is

【式】を有しないアクリレートとし てはテトラエチレングリコールジアクリレート,
テトラヒドロフルフリルアクリレート,トリメチ
ロールプロパントリアクリレート,ペンタエリス
リトールトリアクリレート,ビスフエノールAエ
ポキシアクリレート,フエノールノボラツクエポ
キシアクリレート,クレゾールノボラツクエポキ
シアクリレート,ポリエチレングリコールもしく
はポリエステルとジイソシアネート化合物との反
応生成物をアクリレート化して得られるウレタン
アクリレートなどがある。Rが
Acrylates that do not have [formula] include tetraethylene glycol diacrylate,
Tetrahydrofurfuryl acrylate, trimethylolpropane triacrylate, pentaerythritol triacrylate, bisphenol A epoxy acrylate, phenol novolac epoxy acrylate, cresol novolac epoxy acrylate, the reaction product of polyethylene glycol or polyester and a diisocyanate compound is acrylated. There are urethane acrylates that can be obtained. R is

【式】を有 しないメタクリレートとして2−ヒドロキシエチ
ルメタクリレート,グリシジルメタクリレート,
エチレングリコールジメタクリレート,テトラエ
チレングリコールジメタクリレート,トリメチロ
ールプロパントリメタクリレートなどがある。R
Methacrylates without [formula] include 2-hydroxyethyl methacrylate, glycidyl methacrylate,
These include ethylene glycol dimethacrylate, tetraethylene glycol dimethacrylate, and trimethylolpropane trimethacrylate. R
but

【式】を有するアクリレート及びメタク リレートとしてはモノ(2−アクリロイロキシエ
チル)アシツドホスフエート,モノ(2−メタア
クリロイロキシエチル)アシツドホスフエートな
どがある。 化学式
Examples of acrylates and methacrylates having the formula include mono(2-acryloyloxyethyl) acid phosphate and mono(2-methacryloyloxyethyl) acid phosphate. Chemical formula

【式】で表わされるアクリ レートまたはメタクリレートでRがAcrylic represented by [formula] R is a rate or methacrylate.

【式】 を有しない化合物の一種類以上からなる混合物
100重量部に対してRが
A mixture consisting of one or more types of compounds that do not have [formula]
R per 100 parts by weight

【式】を有する化 合物の一種類以上からなる混合物を0.05〜5重量
部の範囲で含有するのが望ましく、少なすぎると
チツプコンデンサとの密着性改善に効果がなく、
多すぎると硬化性が低下し、部品の接着強度も低
下する。 光増感剤としては2−エチルアントラキノン,
ベンジルジメチルケタール,ベンゾインイソプロ
ピルエーテル,ベンゾインイソブチルエーテル,
1−ヒドロキシシクロヘキシルフエニルケトン,
4−イソプロピル−2−ヒドロキシ−2−メチル
プロピオフエノンなどをアクリレートあるいはメ
タクリレートの混合物100重量部に対して0.1〜5
重量部配合するのが望ましく、0.1重量部より少
ないと光硬化速度が遅く、完全硬化しにくい。5
重量部より多すぎると接着強度が低下するため好
ましくない。 熱重合開始剤としてはt−ブチルパーオキシベ
ンゾエート,t−ブチルパーオキシ(2−エチル
ヘキサノエート),t−ブチルパーオキシイソプ
ロピルカーボネート,t−ブチルパーオキシラウ
レート,過酸化ベンゾイル,1,1−ビス(オー
ブチルパーオキシ)3,3,5−トリメチルシク
ロヘキサン,などをアクリレートまたはメタクリ
レートの混合物100重量部に対して0.1〜10重量部
配合するのが望ましい。0.1重量部より少ないと
硬化性が悪く、10重量部より多すぎると貯蔵安定
性が悪い。 上記以外にさらに無機充填剤を加えて増粘させ
しかもチキソ性を付与して塗布時の糸ひきや広が
りを少なくするのが望ましい。無機充填剤として
タルク,シリカ粉末,超微粒子コロイダルシリカ
(アエロジル)、水酸化アルミニウム,炭酸カルシ
ウム,クレー,有機ベントナイトなどの一種もし
くは2種以上をアクリレートまたはメタクリレー
トの混合物100重量部に対して5〜200重量部の範
囲で使用できる。 貯蔵安定性を良くするためにパラベンゾキノ
ン,ハイドロキノン,ハイドロキノンモノメチル
エーテル,カテコール,2,6−ジ−t−ブチル
−4−メチルフエノールなどの通常の重合禁止剤
が0.01〜0.5重量部の範囲で使用できる。 さらに
It is desirable to contain a mixture consisting of one or more types of compounds having the formula in the range of 0.05 to 5 parts by weight, and if it is too small, it will not be effective in improving the adhesion with the chip capacitor.
If the amount is too large, the curability will decrease and the adhesive strength of the parts will also decrease. As a photosensitizer, 2-ethylanthraquinone,
Benzyl dimethyl ketal, benzoin isopropyl ether, benzoin isobutyl ether,
1-hydroxycyclohexyl phenyl ketone,
0.1 to 5 parts of 4-isopropyl-2-hydroxy-2-methylpropiophenone, etc. per 100 parts by weight of the acrylate or methacrylate mixture.
It is preferable to use parts by weight; if the amount is less than 0.1 part by weight, the photocuring speed will be slow and complete curing will be difficult. 5
If it exceeds the weight part, the adhesive strength will decrease, which is not preferable. As a thermal polymerization initiator, t-butylperoxybenzoate, t-butylperoxy(2-ethylhexanoate), t-butylperoxyisopropyl carbonate, t-butylperoxylaurate, benzoyl peroxide, 1,1 -bis(obutylperoxy)3,3,5-trimethylcyclohexane, etc. is preferably blended in an amount of 0.1 to 10 parts by weight per 100 parts by weight of the acrylate or methacrylate mixture. If it is less than 0.1 parts by weight, the curability will be poor, and if it is more than 10 parts by weight, the storage stability will be poor. In addition to the above, it is desirable to add an inorganic filler to increase the viscosity and impart thixotropy to reduce stringiness and spreading during application. As an inorganic filler, one or more of talc, silica powder, ultrafine colloidal silica (Aerosil), aluminum hydroxide, calcium carbonate, clay, organic bentonite, etc. is added in an amount of 5 to 200 parts per 100 parts by weight of the acrylate or methacrylate mixture. Can be used within a range of parts by weight. To improve storage stability, common polymerization inhibitors such as parabenzoquinone, hydroquinone, hydroquinone monomethyl ether, catechol, and 2,6-di-t-butyl-4-methylphenol are used in the range of 0.01 to 0.5 parts by weight. can. moreover

【式】基を有する化合物は酸性で あるためこれと等価のアミン化合物を配合してで
きるだけ中性に保つのが望ましい。酸性が強いほ
ど、印刷配線基板の銅箔が腐食しやすい。さらに
アミン化合物はアクリル樹脂の重合促進剤として
も作用し、しかも酸素による重合阻害を少なくす
る効果があり樹脂の表面硬化性を良くすることが
できる。アミン化合物としてはジエタノールアミ
ン,トリエタノールアミン,N,N−ジメチルド
デシルアミン,4,4′−ジアミノジフエニルメタ
ン,3,3′−ジアミノジフエニルサルホン,ジエ
チレントリアミンおよびその誘導体,m−フエニ
レンジアミンなどが使用できる。 実施例の説明 次に実施例により詳細に説明する。 実施例 1 表1に示した実施例1の硬化性樹脂組成物を第
1図,第2図に示したようにあらかじめ裏面にリ
ード付電子部品1を挿入したプリント基板2の銅
箔3間にデイスペンサーを用いて塗布して接着剤
層4を形成し、その上に積層チツプコンデンサ5
を載置し、ついで高圧水銀灯(2KW)で高さ8
cmから紫外線を5秒間照射し、さらに遠赤外線加
熱炉に通し、基板表面温度で約150℃,30秒間加
熱し接着剤4の紫外線が当たらなかつた部分を硬
化させた。硬化後のプリント基板の一部について
積層チツプコンデンサとプリント基板とのせん断
方向の接着強度を測定し表1に示した。30個測定
し、平均値をx,最小値をmmとして示した。さら
に、前記硬化後のプリント基板2を250℃の半田
槽に3秒間浸漬し電極部6及びリード線7と銅箔
3とを半田付した。 そのあとすぐにリード線7をカツターで切断
し、噴流式半田槽に250℃,3秒間浸漬した。こ
のような2回半田付後の積層チツプコンデンサの
脱落率は0.05%と良好であつた。 実施例2〜12についても実施例1と同様の方法
で硬化及び半田付を行ない表1に示したように良
好な結果が得られた。 比較例として
Since the compound having the [Formula] group is acidic, it is desirable to mix it with an equivalent amine compound to keep it as neutral as possible. The stronger the acidity, the more likely the copper foil on the printed wiring board will corrode. Furthermore, the amine compound also acts as a polymerization accelerator for acrylic resins, has the effect of reducing polymerization inhibition caused by oxygen, and can improve the surface curability of the resin. Amine compounds include diethanolamine, triethanolamine, N,N-dimethyldodecylamine, 4,4'-diaminodiphenylmethane, 3,3'-diaminodiphenylsulfone, diethylenetriamine and its derivatives, m-phenylenediamine, etc. can be used. Description of Examples Next, examples will be described in detail. Example 1 The curable resin composition of Example 1 shown in Table 1 was applied between the copper foils 3 of a printed circuit board 2 on which a leaded electronic component 1 had been inserted in advance, as shown in FIGS. 1 and 2. An adhesive layer 4 is formed by applying the adhesive using a dispenser, and a multilayer chip capacitor 5 is formed on the adhesive layer 4.
and then lower it to a height of 8 using a high pressure mercury lamp (2KW).
The adhesive 4 was irradiated with ultraviolet rays for 5 seconds from cm, and then passed through a far-infrared heating furnace and heated for 30 seconds at a substrate surface temperature of about 150° C. to harden the parts of the adhesive 4 that were not exposed to the ultraviolet rays. The adhesive strength in the shear direction between the multilayer chip capacitor and the printed circuit board was measured for a part of the printed circuit board after curing, and the results are shown in Table 1. Thirty pieces were measured, and the average value is shown as x and the minimum value as mm. Further, the cured printed circuit board 2 was immersed in a solder bath at 250° C. for 3 seconds to solder the electrode portion 6, lead wire 7, and copper foil 3. Immediately thereafter, the lead wire 7 was cut with a cutter and immersed in a jet soldering bath at 250°C for 3 seconds. The dropout rate of the multilayer chip capacitor after soldering twice was as good as 0.05%. For Examples 2 to 12, curing and soldering were carried out in the same manner as in Example 1, and good results were obtained as shown in Table 1. As a comparative example

【式】を含まない組成物2 種類について実施例1と同様の方法で硬化及び半
田付を行なつた。表1に示したように比較例1と
実施例1の比較では
Two types of compositions not containing [Formula] were cured and soldered in the same manner as in Example 1. As shown in Table 1, in the comparison between Comparative Example 1 and Example 1,

【式】を含むものに比 べて接着強度はほとんど差がないが2回半田付後
の部品脱落率は0.4%と約3倍の値を示している。
比較例2は実施例9に比べて接着強度の最低値が
500gと低く、半田付後の脱落率も2%と極めて
大きかつた。
Compared to those containing [Formula], there is almost no difference in adhesive strength, but the rate of parts falling off after two solderings is 0.4%, about three times as high.
Comparative Example 2 has the lowest value of adhesive strength compared to Example 9.
It was low at 500g, and the dropout rate after soldering was extremely high at 2%.

【表】【table】

【表】 A:ビスフエノールAエポキシアクリレート B:クレゾールノボラツクエポキシアクリレート C:三菱レイヨン(株)製UL−5003 D:トリメチロールプロパントリアクリレート E:2−ヒドロキシエチルメタクリレート F:三菱レイヨン(株)製UT−1002 G:【table】 A: Bisphenol A epoxy acrylate B: Cresol novolac epoxy acrylate C: UL-5003 manufactured by Mitsubishi Rayon Co., Ltd. D: Trimethylolpropane triacrylate E: 2-hydroxyethyl methacrylate F: UT-1002 manufactured by Mitsubishi Rayon Co., Ltd. G:

【式】モノ (2−メタクリロイロキシエチル)アシツドホ
スフエート H: モノ(2−アクリロイロキシエチル)アシツド
ホスフエート I:グリシジルメタクリレート J:テトラエチレングリコールジメタクリレート K: n+m≒4 L:t−ブチルパーオキシベンゾエート M:ベンジルジメチルチタール N:t−ブチルパーオキシ(2−エチルヘキサノ
エート) O:2−エチルアントラキノン P:タルク 発明の効果 以上のように、本発明は硬化性樹脂組成物を使
用するため電子部品との密着性に優れ、半田浸漬
時に電子部品、特に積層チツプコンデンサの脱落
を大幅に削減でき、半田付の信頼性向上と脱落部
品の検査及び修正に要する時間を大幅に削減でき
る。
[Formula] Mono(2-methacryloyloxyethyl) acid phosphate H: Mono(2-acryloyloxyethyl) acid phosphate I: Glycidyl methacrylate J: Tetraethylene glycol dimethacrylate K: n+m≒4 L: t-butyl peroxybenzoate M: benzyl dimethyl tital N: t-butyl peroxy (2-ethylhexanoate) O: 2-ethylanthraquinone P: talc Effects of the invention As described above, the present invention Since the invention uses a curable resin composition, it has excellent adhesion to electronic components, and it can greatly reduce the number of electronic components, especially multilayer chip capacitors, falling off during solder immersion, improving the reliability of soldering and inspecting and inspecting dropped components. The time required for corrections can be significantly reduced.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は電子部品の取付け状態を示す断面図、
第2図は同平面図である。 2……プリント基板、4……接着剤、5……積
層チツプコンデンサ。
Figure 1 is a sectional view showing how electronic parts are installed.
FIG. 2 is a plan view of the same. 2... Printed circuit board, 4... Adhesive, 5... Multilayer chip capacitor.

Claims (1)

【特許請求の範囲】 1 化学式【式】(XはHまたは CH3)で表わされるアクリレートまたはメタクリ
レートでRが【式】基を有する化合物(A) 0.05〜5重量部と、 化学式【式】(XはHまたは CH3)で表わされるアクリレートまたはメタクリ
レートでRが【式】基を有しない化合物で あつて、エポキシアクリレート化合物を少なくと
も含む化合物(B)100重量部と、光増感剤(C)もしく
は熱重合開始剤(D)0.05〜5重量部とを含む硬化性
樹脂組成物を介して印刷配線基板の電子部品搭載
部に電子部品を接着し、これを硬化後、半田付す
る電子部品の取付け方法。
[Scope of Claims] 1 0.05 to 5 parts by weight of a compound (A) of an acrylate or methacrylate represented by the chemical formula [Formula] (X is H or CH 3 ) in which R is a [Formula] group; 100 parts by weight of a compound (B), which is a compound in which X is an acrylate or methacrylate represented by H or CH 3 ) and R does not have a group of [formula], and which contains at least an epoxy acrylate compound, and a photosensitizer (C) Alternatively, the electronic component is bonded to the electronic component mounting area of the printed wiring board via a curable resin composition containing 0.05 to 5 parts by weight of a thermal polymerization initiator (D), and after curing, the electronic component is soldered. Installation method.
JP805784A 1984-01-19 1984-01-19 Method of mounting electronic part Granted JPS60152093A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP805784A JPS60152093A (en) 1984-01-19 1984-01-19 Method of mounting electronic part

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP805784A JPS60152093A (en) 1984-01-19 1984-01-19 Method of mounting electronic part

Publications (2)

Publication Number Publication Date
JPS60152093A JPS60152093A (en) 1985-08-10
JPH0475676B2 true JPH0475676B2 (en) 1992-12-01

Family

ID=11682698

Family Applications (1)

Application Number Title Priority Date Filing Date
JP805784A Granted JPS60152093A (en) 1984-01-19 1984-01-19 Method of mounting electronic part

Country Status (1)

Country Link
JP (1) JPS60152093A (en)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5620008A (en) * 1979-07-27 1981-02-25 Mitsui Toatsu Chem Inc Adhesive resin

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5620008A (en) * 1979-07-27 1981-02-25 Mitsui Toatsu Chem Inc Adhesive resin

Also Published As

Publication number Publication date
JPS60152093A (en) 1985-08-10

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