JP4503239B2 - Flame-retardant adhesive composition, flexible copper-clad laminate, coverlay and adhesive film - Google Patents
Flame-retardant adhesive composition, flexible copper-clad laminate, coverlay and adhesive film Download PDFInfo
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- JP4503239B2 JP4503239B2 JP2003128622A JP2003128622A JP4503239B2 JP 4503239 B2 JP4503239 B2 JP 4503239B2 JP 2003128622 A JP2003128622 A JP 2003128622A JP 2003128622 A JP2003128622 A JP 2003128622A JP 4503239 B2 JP4503239 B2 JP 4503239B2
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- Adhesives Or Adhesive Processes (AREA)
- Non-Metallic Protective Coatings For Printed Circuits (AREA)
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Description
【0001】
【発明の属する技術分野】
本発明は、ハロゲンフリーの難燃性接着剤組成物ならびにそれを用いたフレキシブル銅張積層板、カバーレイおよび接着フィルムに関し、さらには、これらを用いて製造されたプリント配線板に関する。
【0002】
【従来の技術】
近年、世界的な環境問題、人体に対する安全性についての関心の高まりに伴なって、電気・電子機器については、従来からの難燃性に加えて、より少ない有害性、より高い安全性という要求が増大している。すなわち、電気・電子機器は、単に燃えにくいだけでなく、燃焼時に有害ガスや有害煙塵などの発生が少ないことが要望されている。従来、電気・電子機器の配線に使用するフレキシブルプリント配線板は、フレキシブル銅張積層板、カバーレイ及び接着フィルムにより構成されるが、そこに使用されている接着剤には、難燃剤として作用する臭素が含まれる臭素化エポキシ樹脂、特にテトラブロモビスフェノールA型エポキシ樹脂が一般に使用されている。
【0003】
このような臭素化エポキシ樹脂は、良好な難燃性を有するものの、燃焼時に有害なハロゲン化ガス(臭化水素)等を発生することや、ブロモ化ダイオキシン、ブロモ化フラン類を発生する可能性が懸念されているため、その使用が抑制されつつある。
【0004】
一方、カバーレイ、接着フィルムでは硬化前の状態でのハンドリング性が重要であり、このためには、合成ゴムが一般に配合されているが、これを多く含有する接着剤は難燃性に劣り、難燃成分を多く配合する必要があった。
【0005】
【発明が解決しようとする課題】
本発明の目的は、ハロゲンを含まずに良好な難燃性を示す(ハロゲンフリー)とともに、耐熱性、耐折性、電気絶縁性、また、カバーレイ、接着フィルムといった硬化前の状態でのハンドリング性等に優れた接着剤組成物を提供することにある。
【0006】
さらに、本発明は、そのような難燃性接着剤組成物を用いたフレキシブル銅張積層板、カバーレイおよび接着フィルム並びにこれらを用いて製造されたフレキシブルプリント配線板を提供することをも目的とする。
【0007】
【課題を解決するための手段】
本発明者らは、上記の目的を達成しようと鋭意研究を重ねた結果、特定の構造を有するエポキシ樹脂を使用し、接着剤組成物中にホスファゼン化合物、無機充填剤を添加することと、可とう成分として合成ゴムとともにフェノキシ樹脂を配合することで、上記目的が達成されることを見いだし、本発明を完成させたものである。
【0008】
即ち、本発明は、
(A)下記一般式に示すビフェニル骨格及びフェノール骨格を有する多官能樹脂のグリシジル化合物であるエポキシ樹脂、
【化2】
(但し、式中、nは1〜10の整数を表す)
(B)エポキシ用硬化剤、
(C)硬化促進剤、
(D)合成ゴム、
(E)重量平均分子量5000〜100000であるフェノキシ樹脂、
(F)少なくとも1種のホスファゼン化合物および
(G)無機充填剤
を必須成分とし、フェノキシ樹脂がビフェニル骨格又はビスフェノールF骨格を有することを特徴とするハロゲンフリーの難燃性接着剤組成物である。また、上記ハロゲンフリーの難燃性接着剤組成物を用いたフレキシブル銅張積層板、カバーレイおよび接着フィルム並びにこれらを用いて製造されたフレキシブルプリント配線板である。
【0009】
以下、本発明を詳細に説明する。
【0010】
本発明に用いる(A)エポキシ樹脂としては、前記の式化2で示されるビフェニル骨格を含有するような多官能のエポキシ樹脂が好ましく使用できる。またこのエポキシ樹脂は、必要に応じて、1分子中に2個以上のエポキシ基を有するエポキシ樹脂、例えば、ビスフェノールA型エポキシ樹脂、ビスフェノールF型エポキシ樹脂、ノボラック型エポキシ樹脂、グリシジルエーテル型エポキシ樹脂、脂環式エポキシ樹脂、複素環型エポキシ樹脂等のエポキシ樹脂と混合して使用することができる。これらのエポキシ樹脂は、通常、溶剤に溶解して使用することができる。その溶剤は、エポキシ樹脂、エポキシ用硬化剤、エポキシ用硬化促進剤、エラストマーおよびホスファゼンを溶解するものであればよいが、接着剤の塗布乾燥工程において溶剤が残留しないように沸点160℃以下の溶剤であることが望ましい。具体的な溶剤としてはメチルエチルケトン、トルエン、アセトン、エチルセロソルブ、メチルセロソルブ、シクロヘキサノン等が挙げられ、これらは単独又は2種以上混合して使用することができる。
【0011】
本発明に用いる(B)エポキシ用硬化剤としては、通常、エポキシ樹脂の硬化剤に使用されている化合物であれば特に制限なく使用でき、例えば、アミン硬化系としては、ジシアンジアミド(DICY)、芳香族ジアミン等が挙げられ、フェノール硬化系としては、フェノールノボラック樹脂、クレゾールノボラック樹脂、ビスフェノールA型ノボラック樹脂、トリアジン変性フェノールノボラック樹脂等が挙げられ、これらは単独又は2種以上混合して使用することができる。
【0012】
本発明に用いる(C)エポキシ用硬化促進剤としては、通常、エポキシ樹脂の硬化促進剤に使用されているものであり、例えば、2−エチル−4−メチル−イミダゾール、1−ベンジル−2−メチルイミダゾール等のイミダゾール化合物、三フッ化ホウ素アミン錯体、トリフェニルホスフィン等が挙げられ、これらは単独又は2種以上混合して使用することができる。
【0013】
本発明に用いる(D)合成ゴムとしては、特に制限なく接着剤用として用いられているものは広く使用することができる。具体的なものとしては、アクリルゴム、アクリロニトリルブタジエンゴム、カルボキシ含有アクリロニトリルブタジエンゴム等の各種合成ゴムが挙げられ、これらは単独又は2種以上混合して使用することができる。これらの中で、屈曲性、耐折強さに優れるアクリロニトリルブタジエンゴムおよびその変性ゴムが特に好ましく使用される。
【0014】
本発明に用いる(E)フェノキシ樹脂としては、重量平均分子量5000〜100000で、ビフェニル骨格又はビスフェノールF骨格を含有するものが好ましく使用できる。このフェノキシ樹脂は、接着剤組成物の可とう性の向上と難燃性低下防止の目的で配合される。このフェノキシ樹脂の重量平均分子量が5000未満では可とう性付与に効果が小さく、また100000を超えると必須成分である(D)合成ゴムとの相溶性が悪くなり、接着剤溶液の分離を起こしやすく好ましくない。
【0015】
本発明に用いる(F)ホスファゼン化合物としては、実質的にハロゲンを含まないもので、耐熱性、耐湿性、難燃性、耐薬品性等の点から、融点が80℃以上であるホスファゼン化合物を好ましく使用することができる。具体的な例として、下記化学式に示すシクロホスファゼンオリゴマー等が挙げられる。
【0016】
【化3】
(但し、式中Xは水素原子あるいはハロゲンを含まない有機基であって、それらが互いに同じでも異なってもよい。また、nは3〜10の整数を表す)
シクロホスファゼンオリゴマーにおけるハロゲンを含まない有機基Xとしては、アルコキシ基、フェノキシ基、アミノ基、アリル基等が挙げられる。該(F)ホスファゼン化合物の配合割合は、接着剤組成物全体に対して2〜20重量%が好ましい。2重量%未満では十分な難燃性が得られず、また20重量%を超えると接着力が低下して好ましくない。
【0017】
本発明に用いる(G)無機充填剤としては特に制限はなく、タルク、アルミナ、水酸化アルミニウム、水酸化マグネシウム、溶融シリカ、合成シリカ等が挙げられ、これらは単独又は2種以上混合して使用することができる。該無機充填剤の配合割合は、接着剤組成物中の5〜50重量%の割合で配合することが好ましい。配合量が5重量%未満では、十分な難燃性が得られず、また、50重量%を超えると接着剤組成物が硬く脆くなるため、ポリイミドフィルムとの接着力が低下し好ましくない。
【0018】
本発明の接着剤組成物は上述した(A)ビフェニル骨格を含有するような多官能のエポキシ樹脂、(B)エポキシ用硬化剤、(C)エポキシ用硬化促進剤、(D)合成ゴム、(E)重量平均分子量5000〜100000であるフェノキシ樹脂、(F)少なくとも1種のホスファゼン化合物および(G)無機充填剤を必須成分とするが、本発明の目的に反しない限度において、また必要に応じて、微粉末の無機質または有機質の充填剤、顔料、劣化防止剤等を添加配合することができる。上述したこれらの各成分は、メチルエチルケトン、トルエン等の溶剤を用いて、均一に溶解して容易にFPC基板用の接着剤組成物を製造することができる。
【0019】
以上述べた本発明の接着剤組成物は、これをメチルエチルケトン、トルエン、アセトン、エチルセロソルブ、メチルセロソルブ、シクロヘキサノン等の好適な有機溶剤で希釈して樹脂溶液となし、これをポリイミドフィルム上に塗布し、熱ロールで銅箔を片面または両面に貼り合わせた後、加熱硬化するという通常の方法によりフレキシブル銅張積層板を製造することができる。
【0020】
また、本発明の接着剤組成物は、これをメチルエチルケトン、トルエン、アセトン、エチルセロソルブ、メチルセロソルブ、シクロヘキサノン等の好適な有機溶剤で希釈して樹脂溶液となし、これをポリイミドフィルム上に塗布し、加熱乾燥するという通常の方法によりカバーレイを製造することができる。
【0021】
また、本発明の接着剤組成物は、これをメチルエチルケトン、トルエン、アセトン、エチルセロソルブ、メチルセロソルブ、シクロヘキサノン等の好適な有機溶剤で希釈して樹脂溶液となし、キャリアフィルム上に塗布し、加熱乾燥して剥離するという通常の方法により接着フィルムを製造することができる。
【0022】
また、該フレキシブル銅張積層板に回路を形成し、必要であれば穴明けスルーホールメッキを施し、ついで所定箇所に穴を明けた該カバーレイを重ねて加熱加圧成形するという通常の方法でフレキシブルプリント配線板を製造することができる。更にこのフレキシブルプリント配線板に該接着フィルムを介して補強板を重ね合わせ、加熱加圧成形するという通常の方法で補強板付きフレキシブルプリント配線板を製造することができる。
【0023】
また、多層プリント配線板は、該フレキシブルプリント配線板に該接着フィルムを介して該フレキシブル銅張積層板またはハロゲンを含まないガラスエポキシ銅張積層板などを重ね合わせ、加熱加圧成形し、スルーホールを形成し、スルーホールメッキを行った後、所定の回路を形成するという通常の方法により製造することができる。
【0024】
【発明の実施の形態】
以下、本発明を実施例により説明するが、本発明はこれらの実施例によって限定されるものではない。以下の実施例および比較例において「部」とは「重量部」を意味する。
【0025】
実施例1
カルボキシ含有アクリロニトリルブタジエンゴムのニポール1072(日本ゼオン社製商品名)27部、ビフェニル骨格含有多官能型エポキシ樹脂のNC−3000−H(日本化薬社製商品名、エポキシ当量288)34部、4,4′−ジアミノジフェニルスルホン(アミン当量62)5.3部、2−エチル−4−メチルイミダゾール0.3部、テトラメチルタイプのビフェニル型エポキシXY−4000(ジャパンエポキシレジン社製、商品名)とビスフェノールSからなるフェノキシ樹脂溶液YL6746BH30(ジャパンエポキシレジン社製商品名、不揮発分30重量%、重量平均分子量約30000)76.7部、水酸化アルミニウム10部、シクロフェノキシホスファゼンオリゴマー(融点100℃)10部および老化防止剤のN,N′−ジ−2−ナフチル−p−フェニレンジアミン1部を、メチルエチルケトン/トルエン=6/4の混合溶剤に溶解希釈し、固形分30%のFPC基板用の接着剤組成物を製造した。
【0026】
実施例2
カルボキシ含有アクリロニトリルブタジエンゴムのニポール1072(日本ゼオン社製商品名)27部、ビフェニル骨格含有多官能型エポキシ樹脂のNC−3000−H(日本化薬社製商品名、エポキシ当量288)34部、4,4′−ジアミノジフェニルスルホン(アミン当量62)5.3部、2−エチル−4−メチルイミダゾール0.29部、テトラメチルタイプのビフェニル型エポキシXY−4000(ジャパンエポキシレジン社製、商品名)とビスフェノールAからなるフェノキシ樹脂溶液YL6742B40(ジャパンエポキシレジン社製商品名、不揮発分40重量%、重量平均分子量約30000)57.5部、水酸化アルミニウム10部、シクロフェノキシホスファゼンオリゴマー(融点100℃)10部および老化防止剤のN,N′−ジ−2−ナフチル−p−フェニレンジアミン1部を、メチルエチルケトン/トルエン=6/4の混合溶剤に溶解希釈し、固形分30%のFPC基板用の接着剤組成物を製造した。
【0027】
実施例3
カルボキシ含有アクリロニトリルブタジエンゴムのニポール1072(日本ゼオン社製商品名)27部、ビフェニル骨格含有多官能型エポキシ樹脂のNC−3000−H(日本化薬社製商品名、エポキシ当量288)34.5部、4,4′−ジアミノジフェニルスルホン(アミン当量62)5.3部、2−エチル−4−メチルイミダゾール0.3部、ビスフェノールF骨格とビスフェノールA骨格とからなるフェノキシ樹脂YP−70(東都化成社製商品名、重量平均分子量約50000)23部、水酸化アルミニウム10部、シクロフェノキシホスファゼンオリゴマー(融点100℃)10部および老化防止剤のN,N′−ジ−2−ナフチル−p−フェニレンジアミン1部を、メチルエチルケトン/トルエン=6/4の混合溶剤に溶解希釈し、固形分30%のFPC基板用の接着剤組成物を製造した。
【0028】
実施例4
カルボキシ含有アクリロニトリルブタジエンゴムのニポール1072(日本ゼオン社製商品名)27部、ビフェニル骨格含有多官能型エポキシ樹脂のNC−3000−H(日本化薬社製商品名、エポキシ当量288)34.5部、4,4′−ジアミノジフェニルスルホン(アミン当量62)5.4部、2−エチル−4−メチルイミダゾール0.29部、ビスフェノールF骨格からなるフェノキシ樹脂ZX−13950(東都化成社製商品名、重量平均分子量約40000)23部、水酸化アルミニウム10部、シクロフェノキシホスファゼンオリゴマー(融点100℃)10部および老化防止剤のN,N′−ジ−2−ナフチル−p−フェニレンジアミン1部を、メチルエチルケトン/トルエン=6/4の混合溶剤に溶解希釈し、固形分30%のFPC基板用の接着剤組成物を製造した。
【0029】
比較例1
カルボキシ含有アクリロニトリルブタジエンゴムのニポール1072(日本ゼオン社製、商品名)27部、ビフェニル骨格含有多官能型エポキシ樹脂のNC−3000−H(日本化薬社製商品名、エポキシ当量288)34部、4,4′−ジアミノジフェニルスルホン(アミン当量62)5.3部、2−エチル−4−メチルイミダゾール0.29部、ビスフェノールA骨格からなるフェノキシ樹脂溶液エピコート1256B40(ジャパンエポキシレジン社製商品名、不揮発分40重量%、重量平均分子量約50000)57.5部、水酸化アルミニウム10部、シクロフェノキシホスファゼンオリゴマー(融点100℃)10部および老化防止剤のN,N′−ジ−2−ナフチル−p−フェニレンジアミン1部を、メチルエチルケトン/トルエン=6/4の混合溶剤に溶解希釈し、固形分30%のFPC基板用の接着剤組成物を製造した。
【0030】
比較例2
カルボキシ含有アクリロニトリルブタジエンゴムのニポール1072(日本ゼオン社製、商品名)27部、ビフェニル骨格含有多官能型エポキシ樹脂のNC−3000−H(日本化薬社製商品名、エポキシ当量288)55部、4,4′−ジアミノジフェニルスルホン(アミン当量62)8.2部、2−エチル−4−メチルイミダゾール0.27部、水酸化アルミニウム10部、シクロフェノキシホスファゼンオリゴマー(融点100℃)10部および老化防止剤のN,N′−ジ−2−ナフチル−p−フェニレンジアミン1部を、メチルエチルケトン/トルエン=6/4の混合溶剤に溶解希釈し、固形分30%のFPC基板用の接着剤組成物を製造した。
【0031】
比較例3
カルボキシ含有アクリロニトリルブタジエンゴムのニポール1072(日本ゼオン社製、商品名)54部、ビフェニル骨格含有多官能型エポキシ樹脂のNC−3000−H(日本化薬社製商品名、エポキシ当量288)31部、4,4′−ジアミノジフェニルスルホン(アミン当量62)4.7部、2−エチル−4−メチルイミダゾール0.15部、水酸化アルミニウム10部、シクロフェノキシホスファゼンオリゴマー(融点100℃)10部および老化防止剤のN,N′−ジ−2−ナフチル−p−フェニレンジアミン1部を、メチルエチルケトン/トルエン=6/4の混合溶剤に溶解希釈し、固形分30%のFPC基板用の接着剤組成物を製造した。
【0032】
比較例4
カルボキシ含有アクリロニトリルブタジエンゴムのニポール1072(日本ゼオン社製、商品名)54部、ビフェニル骨格含有多官能型エポキシ樹脂のNC−3000−H(日本化薬社製商品名、エポキシ当量288)31部、4,4′−ジアミノジフェニルスルホン(アミン当量62)4.7部、2−エチル−4−メチルイミダゾール0.15部、水酸化アルミニウム10部、シクロフェノキシホスファゼンオリゴマー(融点100℃)30部および老化防止剤のN,N′−ジ−2−ナフチル−p−フェニレンジアミン1部を、メチルエチルケトン/トルエン=6/4の混合溶剤に溶解希釈し、固形分30%のFPC基板用の接着剤組成物を製造した。
【0033】
実施例1〜4および比較例1〜4で製造したFPC基板用の接着剤組成物を厚さ25μmのポリイミドフィルムのカプトン(東レデュポン社製、商品名)にロールコーターで乾燥後の厚さが15μmになるように塗布乾燥し、その接着剤面と銅箔(35μm)の処理面とを重ね合わせて120℃のラミネートロールで圧着した後、オーブンで100℃,3時間、130℃,3時間、160℃,3時間処理し、接着剤を硬化させて8種類のフレキシブル銅張積層板を得た。
【0034】
実施例1〜4および比較例1〜4で製造したFPC基板用の接着剤組成物を、厚さ25μmのポリイミドフィルムのカプトン(東レデュポン社製、商品名)にロールコーターで乾燥後の厚さが35μmになるように塗布乾燥し、半硬化させて8種類のカバーレイを作製した。このカバーレイを、実施例1〜4および比較例1〜4で製造したそれぞれの接着剤組成物を用いて作製したフレキシブル銅張積層板に重ね合わせ、熱プレスで160℃,4MPa,1時間加熱加圧接着し、8種類の評価用のカバーレイ付きフレキシブル基板を作製した。
【0035】
次いで、実施例1〜4および比較例1〜4で製造したFPC基板用の接着剤組成物を、厚さ40μmのポリプロピレンフィルムに、乾燥後の厚さが50μmとなるようにロールコーターで塗布乾燥し、半硬化させて8種類の接着フィルムを作製した。この接着フィルムを厚さ125μmのポリイミド補強板に120℃のラミネートロールで圧着した後、キャリアフィルムのポリプロピレンフィルムを剥がし、実施例1〜4および比較例1〜4で製造したそれぞれの接着剤組成物を用いて作製したフレキシブル銅張積層板のフィルム面に重ね合わせ、熱プレスで160℃,0.5MPa,1時間加熱加圧接着し、8種類の評価用の補強板付きフレキシブル基板を作製した。
【0036】
実施例1〜4および比較例1〜4で製造したFPC基板用の接着剤組成物を用いて得られた8種類の基板についての特性評価を行ったので、実施例1〜4の結果を表1に、比較例1〜4の結果を表2に示す。
【0037】
【表1】
*1:耐燃性試験に用いた試験片は、すべて銅張積層板の銅箔を全面エッチングにより除去して作成した。
【0038】
*2:260℃、280℃および300℃の半田浴に1分間フロートさせて、フクレの有無を確認した。○印…フクレなし、×印…フクレあり。
【0039】
*3:IPC−FC−240Bによる。
【0040】
*4:1mm間隔クシ型テストパターンで測定。
【0041】
*5:プレス前のカバーレイの状態で折り曲げ、ポリイミドフィルムからの接着剤の剥がれ具合を確認した。○印…ハガレなし、×印…ハガレ発生。
【0042】
【表2】
*1:耐燃性試験に用いた試験片は、すべて銅張積層板の銅箔を全面エッチングにより除去して作成した。
【0043】
*2:260℃、280℃および300℃の半田浴に1分間フロートさせて、フクレの有無を確認した。○印…フクレなし、×印…フクレあり。
【0044】
*3:IPC−FC−240Bによる。
【0045】
銅張積層板とカバーレイの組合せで作製したフレキシブル基板のカバーレイを剥離して作製。
【0046】
*4:1mm間隔クシ型テストパターンで測定。
【0047】
*5:プレス前のカバーレイの状態で折り曲げ、ポリイミドフィルムからの接着剤の剥がれ具合を確認した。○印…ハガレなし、×印…ハガレ発生。
【0048】
【発明の効果】
以上の説明および表1、2から明らかなように、本発明によれば、塩素、臭素を実質的に含有しないで優れた難燃性を示し、しかもカバーレイ、接着剤フィルムなどの硬化前の状態でハドリング性に優れる接着剤が提供される。このような材料を用いれば、良好な環境特性を付与し、かつ種々の特性に優れたフレキシブルプリント配線板を製造することができる。[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a halogen-free flame-retardant adhesive composition, a flexible copper-clad laminate using the same, a coverlay and an adhesive film, and further to a printed wiring board produced using these.
[0002]
[Prior art]
In recent years, with the growing concern about global environmental issues and human safety, electrical and electronic devices require less harmfulness and higher safety in addition to conventional flame retardancy. Has increased. That is, electrical / electronic devices are not only difficult to burn, but are also required to generate less harmful gases and harmful smoke during combustion. Conventionally, a flexible printed wiring board used for wiring of electric / electronic devices is composed of a flexible copper-clad laminate, a coverlay and an adhesive film, but acts as a flame retardant on the adhesive used there. Brominated epoxy resins containing bromine, particularly tetrabromobisphenol A type epoxy resins are generally used.
[0003]
Although such brominated epoxy resins have good flame retardancy, they may generate harmful halogenated gas (hydrogen bromide), etc. during combustion, and may generate brominated dioxins and brominated furans. The use is being suppressed because of concerns.
[0004]
On the other hand, handling properties in the state before curing are important for coverlays and adhesive films, and for this purpose, synthetic rubber is generally blended, but adhesives containing many of these are inferior in flame retardancy, It was necessary to add a lot of flame retardant components.
[0005]
[Problems to be solved by the invention]
The object of the present invention is to display good flame retardancy without halogen (halogen-free), heat resistance, folding resistance, electrical insulation, and handling before curing such as coverlay and adhesive film It is providing the adhesive composition excellent in property etc.
[0006]
Furthermore, the present invention also aims to provide a flexible copper-clad laminate, a coverlay and an adhesive film using such a flame-retardant adhesive composition, and a flexible printed wiring board produced using these. To do.
[0007]
[Means for Solving the Problems]
As a result of intensive research aimed at achieving the above object, the present inventors have used an epoxy resin having a specific structure, added a phosphazene compound and an inorganic filler into the adhesive composition, and It has been found that the above object can be achieved by blending a phenoxy resin together with a synthetic rubber as a component, and the present invention has been completed.
[0008]
That is, the present invention
(A) an epoxy resin that is a glycidyl compound of a polyfunctional resin having a biphenyl skeleton and a phenol skeleton represented by the following general formula:
[Chemical 2]
(In the formula, n represents an integer of 1 to 10)
(B) a curing agent for epoxy,
(C) a curing accelerator,
(D) synthetic rubber,
(E) a phenoxy resin having a weight average molecular weight of 5,000 to 100,000,
(F) A halogen-free flame-retardant adhesive composition comprising at least one phosphazene compound and (G) an inorganic filler as essential components, wherein the phenoxy resin has a biphenyl skeleton or a bisphenol F skeleton. The present invention also provides a flexible copper-clad laminate, a coverlay and an adhesive film using the halogen-free flame-retardant adhesive composition, and a flexible printed wiring board produced using these.
[0009]
Hereinafter, the present invention will be described in detail.
[0010]
As the (A) epoxy resin used in the present invention, a polyfunctional epoxy resin containing a biphenyl skeleton represented by the above formula 2 can be preferably used. The epoxy resin may be an epoxy resin having two or more epoxy groups in one molecule, for example, bisphenol A type epoxy resin, bisphenol F type epoxy resin, novolac type epoxy resin, glycidyl ether type epoxy resin, if necessary. It can be used by mixing with an epoxy resin such as an alicyclic epoxy resin or a heterocyclic epoxy resin. These epoxy resins can usually be used by dissolving in a solvent. The solvent may be any solvent that dissolves epoxy resin, epoxy curing agent, epoxy curing accelerator, elastomer and phosphazene, but has a boiling point of 160 ° C. or lower so that the solvent does not remain in the coating and drying process of the adhesive. It is desirable that Specific examples of the solvent include methyl ethyl ketone, toluene, acetone, ethyl cellosolve, methyl cellosolve, and cyclohexanone, and these can be used alone or in combination of two or more.
[0011]
The (B) epoxy curing agent used in the present invention can be used without particular limitation as long as it is usually a compound used as an epoxy resin curing agent. Examples of amine curing systems include dicyandiamide (DICY), aromatic Examples of phenolic curing systems include phenol novolak resins, cresol novolak resins, bisphenol A type novolak resins, triazine-modified phenol novolak resins, and the like. These may be used alone or in combination of two or more. Can do.
[0012]
The (C) epoxy curing accelerator used in the present invention is usually used as an epoxy resin curing accelerator. Examples thereof include 2-ethyl-4-methyl-imidazole and 1-benzyl-2- Examples thereof include imidazole compounds such as methylimidazole, boron trifluoride amine complex, and triphenylphosphine, and these can be used alone or in combination of two or more.
[0013]
As the synthetic rubber (D) used in the present invention, those used for adhesives without particular limitation can be widely used. Specific examples include various synthetic rubbers such as acrylic rubber, acrylonitrile butadiene rubber, and carboxy-containing acrylonitrile butadiene rubber, and these can be used alone or in combination of two or more. Among these, acrylonitrile butadiene rubber excellent in flexibility and bending strength and its modified rubber are particularly preferably used.
[0014]
As the (E) phenoxy resin used in the present invention, a resin having a weight average molecular weight of 5,000 to 100,000 and containing a biphenyl skeleton or a bisphenol F skeleton can be preferably used. This phenoxy resin is blended for the purpose of improving the flexibility of the adhesive composition and preventing flame retardancy. If the weight average molecular weight of the phenoxy resin is less than 5,000, the effect of imparting flexibility is small, and if it exceeds 100,000, the compatibility with the essential component (D) synthetic rubber is deteriorated and the adhesive solution is easily separated. It is not preferable.
[0015]
As the phosphazene compound (F) used in the present invention, a phosphazene compound which is substantially free of halogen and has a melting point of 80 ° C. or higher from the viewpoint of heat resistance, moisture resistance, flame retardancy, chemical resistance and the like. It can be preferably used. Specific examples include cyclophosphazene oligomers represented by the following chemical formula.
[0016]
[Chemical 3]
(Wherein, X is an organic group containing no hydrogen atom or halogen, and they may be the same or different from each other. N represents an integer of 3 to 10)
Examples of the halogen-free organic group X in the cyclophosphazene oligomer include an alkoxy group, a phenoxy group, an amino group, and an allyl group. The blending ratio of the (F) phosphazene compound is preferably 2 to 20% by weight with respect to the entire adhesive composition. If it is less than 2% by weight, sufficient flame retardancy cannot be obtained, and if it exceeds 20% by weight, the adhesive strength is lowered, which is not preferable.
[0017]
There is no restriction | limiting in particular as an inorganic filler (G) used for this invention, A talc, an alumina, aluminum hydroxide, magnesium hydroxide, a fused silica, a synthetic silica etc. are mentioned, These are used individually or in mixture of 2 or more types. can do. It is preferable to mix | blend the mixture ratio of this inorganic filler in the ratio of 5 to 50 weight% in an adhesive composition. If the blending amount is less than 5% by weight, sufficient flame retardancy cannot be obtained. If the blending amount exceeds 50% by weight, the adhesive composition becomes hard and brittle.
[0018]
The adhesive composition of the present invention comprises (A) a polyfunctional epoxy resin containing a biphenyl skeleton, (B) a curing agent for epoxy, (C) a curing accelerator for epoxy, (D) a synthetic rubber, ( E) A phenoxy resin having a weight average molecular weight of 5,000 to 100,000, (F) at least one phosphazene compound, and (G) an inorganic filler as essential components, but as long as they do not contradict the purpose of the present invention, and as necessary In addition, finely divided inorganic or organic fillers, pigments, deterioration inhibitors and the like can be added and blended. These components described above can be dissolved uniformly using a solvent such as methyl ethyl ketone and toluene, and an adhesive composition for an FPC board can be easily produced.
[0019]
The adhesive composition of the present invention described above is diluted with a suitable organic solvent such as methyl ethyl ketone, toluene, acetone, ethyl cellosolve, methyl cellosolve, cyclohexanone to form a resin solution, which is applied onto a polyimide film. A flexible copper-clad laminate can be manufactured by the usual method of sticking copper foil on one or both sides with a heat roll and then heat-curing.
[0020]
Further, the adhesive composition of the present invention is diluted with a suitable organic solvent such as methyl ethyl ketone, toluene, acetone, ethyl cellosolve, methyl cellosolve, cyclohexanone to form a resin solution, which is applied onto a polyimide film, A coverlay can be manufactured by the usual method of drying by heating.
[0021]
In addition, the adhesive composition of the present invention is diluted with a suitable organic solvent such as methyl ethyl ketone, toluene, acetone, ethyl cellosolve, methyl cellosolve, cyclohexanone to form a resin solution, which is applied onto a carrier film and dried by heating. Then, an adhesive film can be produced by a usual method of peeling.
[0022]
In addition, a circuit is formed on the flexible copper-clad laminate, and through-hole plating is performed if necessary, and then the cover lay with holes formed in predetermined positions is stacked and heated and pressed. A flexible printed wiring board can be manufactured. Further, a flexible printed wiring board with a reinforcing plate can be manufactured by a normal method of superimposing a reinforcing plate on the flexible printed wiring board via the adhesive film, followed by heat and pressure molding.
[0023]
In addition, the multilayer printed wiring board is formed by superposing the flexible copper-clad laminate or the halogen-free glass epoxy copper-clad laminate on the flexible printed wiring board via the adhesive film, heating and pressing, and through holes. After a through hole plating is performed, a predetermined circuit can be formed by a normal method.
[0024]
DETAILED DESCRIPTION OF THE INVENTION
EXAMPLES Hereinafter, although an Example demonstrates this invention, this invention is not limited by these Examples. In the following Examples and Comparative Examples, “parts” means “parts by weight”.
[0025]
Example 1
27 parts Nipol 1072 (trade name, manufactured by Nippon Zeon Co., Ltd.) of carboxy-containing acrylonitrile butadiene rubber, 34 parts of NC-3000-H (trade name, manufactured by Nippon Kayaku Co., Ltd., epoxy equivalent 288), a polyfunctional epoxy resin containing biphenyl skeleton, 4 parts , 4'-diaminodiphenylsulfone (amine equivalent 62) 5.3 parts, 2-ethyl-4-methylimidazole 0.3 parts, tetramethyl type biphenyl type epoxy XY-4000 (trade name, manufactured by Japan Epoxy Resin Co., Ltd.) And bisphenol S phenoxy resin solution YL6746BH30 (trade name, Japan Epoxy Resin, trade name, nonvolatile content 30% by weight, weight average molecular weight about 30000) 76.7 parts, aluminum hydroxide 10 parts, cyclophenoxyphosphazene oligomer (melting point 100 ° C.) 10 parts and anti-aging agent The N'- di-2-naphthyl -p- phenylenediamine, 1 part Methyl ethyl ketone / toluene = 6/4 mixture was dissolved diluted in a solvent, to produce an adhesive composition for a solid content of 30% FPC substrate.
[0026]
Example 2
27 parts Nipol 1072 (trade name, manufactured by Nippon Zeon Co., Ltd.) of carboxy-containing acrylonitrile butadiene rubber, 34 parts of NC-3000-H (trade name, manufactured by Nippon Kayaku Co., Ltd., epoxy equivalent 288), a polyfunctional epoxy resin containing biphenyl skeleton, 4 parts , 4′-diaminodiphenylsulfone (amine equivalent 62) 5.3 parts, 2-ethyl-4-methylimidazole 0.29 parts, tetramethyl type biphenyl type epoxy XY-4000 (trade name, manufactured by Japan Epoxy Resin Co., Ltd.) And bisphenol A phenoxy resin solution YL6742B40 (trade name, manufactured by Japan Epoxy Resin Co., Ltd., non-volatile content 40% by weight, weight average molecular weight about 30000) 57.5 parts, aluminum hydroxide 10 parts, cyclophenoxyphosphazene oligomer (melting point 100 ° C.) 10 parts and anti-aging agent The N'- di-2-naphthyl -p- phenylenediamine, 1 part Methyl ethyl ketone / toluene = 6/4 mixture was dissolved diluted in a solvent, to produce an adhesive composition for a solid content of 30% FPC substrate.
[0027]
Example 3
27 parts of Nipol 1072 (trade name, manufactured by Nippon Zeon Co., Ltd.) of carboxy-containing acrylonitrile butadiene rubber, 34.5 parts of NC-3000-H (trade name, manufactured by Nippon Kayaku Co., Ltd., epoxy equivalent 288) of polyfunctional epoxy resin containing biphenyl skeleton , 4,4'-diaminodiphenylsulfone (amine equivalent 62) 5.3 parts, 2-ethyl-4-methylimidazole 0.3 parts, phenoxy resin YP-70 (Tohto Kasei Co., Ltd.) comprising bisphenol F skeleton and bisphenol A skeleton Product name, weight average molecular weight of about 50000) 23 parts, aluminum hydroxide 10 parts, cyclophenoxyphosphazene oligomer (melting point 100 ° C.) 10 parts and anti-aging agent N, N′-di-2-naphthyl-p-phenylene 1 part of diamine is dissolved and diluted in a mixed solvent of methyl ethyl ketone / toluene = 6/4 It was prepared an adhesive composition for a solid content of 30% FPC substrate.
[0028]
Example 4
27 parts of Nipol 1072 (trade name, manufactured by Nippon Zeon Co., Ltd.) of carboxy-containing acrylonitrile butadiene rubber, 34.5 parts of NC-3000-H (trade name, manufactured by Nippon Kayaku Co., Ltd., epoxy equivalent 288) of polyfunctional epoxy resin containing biphenyl skeleton , 4,4'-diaminodiphenylsulfone (amine equivalent 62) 5.4 parts, 2-ethyl-4-methylimidazole 0.29 parts, phenoxy resin ZX-13950 (trade name, manufactured by Tohto Kasei Co., Ltd., Weight average molecular weight of about 40,000) 23 parts, aluminum hydroxide 10 parts, cyclophenoxyphosphazene oligomer (melting point 100 ° C.) 10 parts and anti-aging agent N, N′-di-2-naphthyl-p-phenylenediamine 1 part, Dissolved and diluted in a mixed solvent of methyl ethyl ketone / toluene = 6/4, solid content 30% The adhesive composition of the FPC board was produced.
[0029]
Comparative Example 1
27 parts of Nipol 1072 (trade name, manufactured by Nippon Zeon Co., Ltd.) of carboxy-containing acrylonitrile butadiene rubber, 34 parts of NC-3000-H (trade name, manufactured by Nippon Kayaku Co., Ltd., epoxy equivalent 288) of polyfunctional epoxy resin containing biphenyl skeleton, Phenoxy resin solution Epicoat 1256B40 consisting of 5.3 parts of 4,4'-diaminodiphenylsulfone (amine equivalent 62), 0.29 parts of 2-ethyl-4-methylimidazole and bisphenol A skeleton (trade name, manufactured by Japan Epoxy Resin Co., Ltd.) Non-volatile content 40% by weight, weight average molecular weight of about 50000) 57.5 parts, aluminum hydroxide 10 parts, cyclophenoxyphosphazene oligomer (melting point 100 ° C.) 10 parts and anti-aging agent N, N′-di-2-naphthyl- 1 part of p-phenylenediamine is added to methyl ethyl ketone / torr Was dissolved diluted in a mixed solvent of emission = 6/4 was prepared an adhesive composition for a solid content of 30% FPC substrate.
[0030]
Comparative Example 2
27 parts of Nipol 1072 (trade name, manufactured by Nippon Zeon Co., Ltd.) of carboxy-containing acrylonitrile butadiene rubber, 55 parts of NC-3000-H (trade name, epoxy equivalent 288, manufactured by Nippon Kayaku Co., Ltd.) containing a biphenyl skeleton-containing polyfunctional epoxy resin, 8.2 parts of 4,4′-diaminodiphenylsulfone (amine equivalent 62), 0.27 parts of 2-ethyl-4-methylimidazole, 10 parts of aluminum hydroxide, 10 parts of cyclophenoxyphosphazene oligomer (melting point 100 ° C.) and aging 1 part of N, N'-di-2-naphthyl-p-phenylenediamine as an inhibitor is dissolved and diluted in a mixed solvent of methyl ethyl ketone / toluene = 6/4, and an adhesive composition for an FPC board having a solid content of 30% Manufactured.
[0031]
Comparative Example 3
54 parts of Nipol 1072 (trade name, manufactured by Nippon Zeon Co., Ltd.) of carboxy-containing acrylonitrile butadiene rubber, 31 parts of NC-3000-H (trade name, manufactured by Nippon Kayaku Co., Ltd., epoxy equivalent 288) of polyfunctional epoxy resin containing biphenyl skeleton, 4.7 parts of 4,4′-diaminodiphenylsulfone (amine equivalent 62), 0.15 parts of 2-ethyl-4-methylimidazole, 10 parts of aluminum hydroxide, 10 parts of cyclophenoxyphosphazene oligomer (melting point 100 ° C.) and aging 1 part of N, N'-di-2-naphthyl-p-phenylenediamine as an inhibitor is dissolved and diluted in a mixed solvent of methyl ethyl ketone / toluene = 6/4, and an adhesive composition for an FPC board having a solid content of 30% Manufactured.
[0032]
Comparative Example 4
54 parts of Nipol 1072 (trade name, manufactured by Nippon Zeon Co., Ltd.) of carboxy-containing acrylonitrile butadiene rubber, 31 parts of NC-3000-H (trade name, manufactured by Nippon Kayaku Co., Ltd., epoxy equivalent 288) of polyfunctional epoxy resin containing biphenyl skeleton, 4.7 parts of 4,4′-diaminodiphenylsulfone (amine equivalent 62), 0.15 parts of 2-ethyl-4-methylimidazole, 10 parts of aluminum hydroxide, 30 parts of cyclophenoxyphosphazene oligomer (melting point 100 ° C.) and aging 1 part of N, N'-di-2-naphthyl-p-phenylenediamine as an inhibitor is dissolved and diluted in a mixed solvent of methyl ethyl ketone / toluene = 6/4, and an adhesive composition for an FPC board having a solid content of 30% Manufactured.
[0033]
The adhesive composition for FPC boards produced in Examples 1 to 4 and Comparative Examples 1 to 4 has a thickness after drying with a roll coater on a 25 μm thick polyimide film Kapton (trade name, manufactured by Toray DuPont). After coating and drying to 15 μm, the adhesive surface and the treated surface of copper foil (35 μm) are overlapped and pressure-bonded with a laminate roll at 120 ° C., and then oven is 100 ° C., 3 hours, 130 ° C., 3 hours. The adhesive was cured by treating at 160 ° C. for 3 hours to obtain 8 types of flexible copper-clad laminates.
[0034]
The thickness of the adhesive composition for FPC boards produced in Examples 1 to 4 and Comparative Examples 1 to 4 after being dried with a roll coater on a 25 μm thick polyimide film Kapton (trade name, manufactured by Toray DuPont) Was coated and dried so as to be 35 μm, and semi-cured to prepare 8 types of coverlays. This coverlay was overlaid on the flexible copper clad laminate produced using each adhesive composition produced in Examples 1 to 4 and Comparative Examples 1 to 4, and heated at 160 ° C., 4 MPa for 1 hour with a hot press. Pressure bonding was performed to prepare eight types of flexible substrates with coverlays for evaluation.
[0035]
Next, the FPC board adhesive compositions produced in Examples 1 to 4 and Comparative Examples 1 to 4 were applied and dried on a 40 μm thick polypropylene film with a roll coater so that the thickness after drying was 50 μm. And semi-cured to prepare 8 types of adhesive films. Each adhesive composition produced in Examples 1 to 4 and Comparative Examples 1 to 4 was prepared by pressure-bonding the adhesive film to a polyimide reinforcing plate having a thickness of 125 μm with a laminate roll at 120 ° C. and then removing the polypropylene film of the carrier film. Was laminated on the film surface of the flexible copper-clad laminate produced using the above, and heat-press bonded for 1 hour at 160 ° C., 0.5 MPa by hot pressing to produce 8 types of flexible substrates with reinforcing plates for evaluation.
[0036]
Since the characteristic evaluation about 8 types of board | substrates obtained using the adhesive composition for FPC boards manufactured in Examples 1-4 and Comparative Examples 1-4 was performed, the result of Examples 1-4 is represented. Table 1 shows the results of Comparative Examples 1 to 4.
[0037]
[Table 1]
* 1: All test pieces used for the flame resistance test were prepared by removing the copper foil of the copper clad laminate by etching the entire surface.
[0038]
* 2: Float in a solder bath at 260 ° C., 280 ° C. and 300 ° C. for 1 minute to confirm the presence or absence of swelling. ○: No blister, x: Buff.
[0039]
* 3: According to IPC-FC-240B.
[0040]
* 4: Measured with a 1 mm spacing comb type test pattern.
[0041]
* 5: It was bent in the state of the cover lay before pressing, and the degree of peeling of the adhesive from the polyimide film was confirmed. ○ mark: no peeling, x mark: peeling.
[0042]
[Table 2]
* 1: All test pieces used for the flame resistance test were prepared by removing the copper foil of the copper clad laminate by etching the entire surface.
[0043]
* 2: Float in a solder bath at 260 ° C., 280 ° C. and 300 ° C. for 1 minute to confirm the presence or absence of swelling. ○: No blister, x: Buff.
[0044]
* 3: According to IPC-FC-240B.
[0045]
Fabricated by peeling the coverlay of a flexible board made from a combination of copper-clad laminate and coverlay.
[0046]
* 4: Measured with a 1 mm spacing comb type test pattern.
[0047]
* 5: It was bent in the state of the cover lay before pressing, and the degree of peeling of the adhesive from the polyimide film was confirmed. ○ mark: no peeling, x mark: peeling.
[0048]
【The invention's effect】
As is apparent from the above description and Tables 1 and 2, according to the present invention, excellent flame retardancy is exhibited without substantially containing chlorine and bromine, and before curing of the coverlay, adhesive film, etc. An adhesive having excellent hadling properties in a state is provided. By using such a material, it is possible to produce a flexible printed wiring board that imparts favorable environmental characteristics and is excellent in various characteristics.
Claims (7)
(B)エポキシ用硬化剤、
(C)硬化促進剤、
(D)合成ゴム、
(E)重量平均分子量5000〜100000であるビフェニル骨格又はビスフェノールF骨格を有するフェノキシ樹脂、
(F)少なくとも1種のホスファゼン化合物および
(G)無機充填剤
を必須成分とすることを特徴とするハロゲンフリーの難燃性接着剤組成物。(A) an epoxy resin that is a glycidyl compound of a polyfunctional resin having a biphenyl skeleton and a phenol skeleton represented by the following general formula:
(B) a curing agent for epoxy,
(C) a curing accelerator,
(D) synthetic rubber,
(E) a phenoxy resin having a biphenyl skeleton or a bisphenol F skeleton having a weight average molecular weight of 5000 to 100,000,
(F) A halogen-free flame-retardant adhesive composition comprising at least one phosphazene compound and (G) an inorganic filler as essential components.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2003128622A JP4503239B2 (en) | 2003-05-07 | 2003-05-07 | Flame-retardant adhesive composition, flexible copper-clad laminate, coverlay and adhesive film |
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| JP2003128622A JP4503239B2 (en) | 2003-05-07 | 2003-05-07 | Flame-retardant adhesive composition, flexible copper-clad laminate, coverlay and adhesive film |
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| JP2004331783A JP2004331783A (en) | 2004-11-25 |
| JP4503239B2 true JP4503239B2 (en) | 2010-07-14 |
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Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4600640B2 (en) * | 2003-11-10 | 2010-12-15 | 信越化学工業株式会社 | Acrylic adhesive sheet |
| JP4584619B2 (en) * | 2004-04-30 | 2010-11-24 | 信越化学工業株式会社 | Flame-retardant adhesive composition and adhesive sheet using the same |
| JP2006316234A (en) * | 2005-04-13 | 2006-11-24 | Shin Etsu Chem Co Ltd | Flame-retardant adhesive composition, and adhesive sheet, coverlay film and flexible copper-clad laminate using the same |
| JP5516657B2 (en) * | 2005-05-27 | 2014-06-11 | 日立化成株式会社 | Metal foil with adhesion aid, printed wiring board using the same, and method for producing the same |
| JP2007224162A (en) * | 2006-02-23 | 2007-09-06 | Matsushita Electric Works Ltd | Flame-retardant resin composition, prepreg, resin sheet, and molded product |
| TWI445790B (en) * | 2007-02-28 | 2014-07-21 | Nippon Steel & Sumikin Chem Co | A flame retardant adhesive resin composition, and a flexible printed circuit board material using the same |
| JP2008208311A (en) * | 2007-02-28 | 2008-09-11 | Kyocera Chemical Corp | Adhesive composition for flexible printed wiring board and flexible printed wiring board using the same |
| KR100959746B1 (en) | 2007-10-23 | 2010-05-25 | 제일모직주식회사 | Adhesive film composition and adhesive film for semiconductor assembly using phenoxy resin and ester-based thermoplastic |
| JP5485521B2 (en) * | 2008-05-26 | 2014-05-07 | 新日鉄住金化学株式会社 | Flame-retardant adhesive resin composition and adhesive film, coverlay film and flexible copper-clad laminate using the same |
| KR20130037205A (en) * | 2010-07-14 | 2013-04-15 | 교세라 케미카르 가부시키가이샤 | Flexible wiring board, dry film for coverlay, and production method for flexible wiring board |
| CN102311612B (en) * | 2011-04-03 | 2013-05-01 | 广东生益科技股份有限公司 | Resin composition and resin coated copper foil made of same |
| CN103694639B (en) * | 2013-12-19 | 2016-03-09 | 广东生益科技股份有限公司 | A kind of Halogen ageing-resistant epoxy resin composition and prepare the method for mulch film with this resin combination |
| JP7766282B2 (en) * | 2020-07-08 | 2025-11-10 | パナソニックIpマネジメント株式会社 | Insulating resin material and printed wiring board |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0823165A (en) * | 1994-07-08 | 1996-01-23 | Hitachi Chem Co Ltd | Manufacture of metal cored wiring board using copper foil with insulating bonding agent |
| JP3411748B2 (en) * | 1996-05-09 | 2003-06-03 | 日立化成工業株式会社 | Metal foil with adhesive, adhesive sheet and multilayer wiring board |
| JP3810954B2 (en) * | 1999-07-12 | 2006-08-16 | 京セラケミカル株式会社 | Flame-retardant adhesive composition, flexible copper-clad laminate, coverlay and adhesive film |
| JP4423779B2 (en) * | 1999-10-13 | 2010-03-03 | 味の素株式会社 | Epoxy resin composition, adhesive film and prepreg using the composition, multilayer printed wiring board using the same, and method for producing the same |
| JP2002194310A (en) * | 2000-12-25 | 2002-07-10 | Toray Ind Inc | Adhesive composition for semiconductor device, adhesive sheet for semiconductor device and coverlay film using the same |
| JP2003100953A (en) * | 2001-06-29 | 2003-04-04 | Hitachi Chem Co Ltd | Adhesive member |
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| JP2004331783A (en) | 2004-11-25 |
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