JP4911252B1 - カルボキシル基含有変性エステル樹脂を含む熱硬化性樹脂組成物 - Google Patents
カルボキシル基含有変性エステル樹脂を含む熱硬化性樹脂組成物 Download PDFInfo
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- JP4911252B1 JP4911252B1 JP2011054067A JP2011054067A JP4911252B1 JP 4911252 B1 JP4911252 B1 JP 4911252B1 JP 2011054067 A JP2011054067 A JP 2011054067A JP 2011054067 A JP2011054067 A JP 2011054067A JP 4911252 B1 JP4911252 B1 JP 4911252B1
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- PADOFXALCIVUFS-UHFFFAOYSA-N tris(2,3-dimethoxyphenyl)phosphane Chemical compound COC1=CC=CC(P(C=2C(=C(OC)C=CC=2)OC)C=2C(=C(OC)C=CC=2)OC)=C1OC PADOFXALCIVUFS-UHFFFAOYSA-N 0.000 description 1
- GRPURDFRFHUDSP-UHFFFAOYSA-N tris(prop-2-enyl) benzene-1,2,4-tricarboxylate Chemical compound C=CCOC(=O)C1=CC=C(C(=O)OCC=C)C(C(=O)OCC=C)=C1 GRPURDFRFHUDSP-UHFFFAOYSA-N 0.000 description 1
- GTOWTBKGCUDSNY-UHFFFAOYSA-K tris[[ethyl(methyl)phosphoryl]oxy]alumane Chemical compound [Al+3].CCP(C)([O-])=O.CCP(C)([O-])=O.CCP(C)([O-])=O GTOWTBKGCUDSNY-UHFFFAOYSA-K 0.000 description 1
- BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/91—Polymers modified by chemical after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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Abstract
【解決手段】ポリオール化合物(a)と脂環式多塩基酸無水物または芳香族多塩基酸無水物である酸無水物基含有化合物(b)とを反応させてカルボキシル基含有エステル樹脂(c)を生成し、前記カルボキシル基含有エステル樹脂(c)と1分子中に少なくとも2個のエポキシ基を有するエポキシ化合物(d)とを反応させて側鎖ヒドロキシル基含有変性エステル樹脂(e)を生成し、さらに、側鎖ヒドロキシル基含有変性エステル樹脂(e)に、酸無水物基含有化合物(b)を反応させてなるカルボキシル基含有変性エステル樹脂(A)を含む熱硬化性樹脂組成物。
【選択図】なし
Description
(2)カバーレイフィルム用接着剤:カバーレイフィルム(回路の最表面を保護する目的で用いられるポリイミドフィルムなど)と、下地の回路基板と、を張り合わせるために用いられ、あらかじめポリイミドフィルムと、接着層とが一体化されているものが多い。
(3)銅張フィルム(CCL)用接着剤:ポリイミドフィルムと銅箔とを張り合わせるために用いられる。銅回路形成時にエッチング等の加工が施される。
(4)カバーレイ:回路の最表面を保護する目的で用いられ、回路上に印刷インクを印刷したり、接着シートを張り合わせたりした後、硬化させることで形成される。感光性や熱硬化性のものがある。
(5)補強板用接着剤:配線板の機械的強度を補完する目的で、配線板の一部を、金属、ガラスエポキシ、ポリイミド等の補強板に固定するために用いられる。
(6)電磁波シールド用接着剤:電子回路から発生する電磁ノイズを遮蔽する目的で、フレキシブルプリント配線板に貼着される。
すなわち、第1の発明は、カルボキシル基含有変性エステル樹脂(A)、
エポキシ基含有化合物、イソシアネート基含有化合物、およびブロック化イソシアネート基含有化合物からなる群より選ばれる少なくとも一種である化合物(B)、
および熱硬化助剤(C)を含む熱硬化性樹脂組成物であって、
カルボキシル基含有変性エステル樹脂(A)が、
ポリオール化合物(a)と、脂環式多塩基酸無水物および芳香族多塩基酸無水物から選ばれる少なくとも1種である酸無水物基含有化合物(b)とを反応させてカルボキシル基含有エステル樹脂(c)を生成し、
前記カルボキシル基含有エステル樹脂(c)と1分子中に少なくとも2個のエポキシ基を有するエポキシ化合物(d)とを反応させて側鎖ヒドロキシル基含有変性エステル樹脂(e)を生成し、
さらに、側鎖ヒドロキシル基含有変性エステル樹脂(e)に脂環式多塩基酸無水物および芳香族多塩基酸無水物から選ばれる少なくとも1種である酸無水物基含有化合物(b)を反応させてなることを特徴とする熱硬化性樹脂組成物に関する。
さらにまた、第8の発明は、第7の発明の硬化物からなる層を有することを特徴とするプリント配線板に関する。
これは出発原料に、ポリオール化合物(a)と脂環式多塩基酸無水物および芳香族多塩基酸無水物から選ばれる少なくとも1種である酸無水物基含有化合物(b)とを用いているためであり、従来の二塩基酸を原料としたポリエステル骨格を主鎖として用いた樹脂に比べ、ポリオール化合物(a)由来のフレキシブル性や加工性等を付与できるからである。また、ポリオール化合物(a)と脂環式多塩基酸無水物および芳香族多塩基酸無水物から選ばれる少なくとも1種である酸無水物基含有化合物(b)によってカルボキシル基含有エステル樹脂(c)を生成する際に、絶縁信頼性に劣るとされているエステル結合基が嵩高い置換基で保護されるため、従来のポリエステル骨格を主鎖として用いた樹脂に比べ、絶縁信頼性、半田耐熱性等を著しく向上できるのである。
−[−R8−O−CO−]m−
(式中、R8は、2価の有機残基、mは、1以上の整数を表す。)
ヘキサンジオール、メチルヘキサンジオール、ヘプタンジオール、オクタンジオール若しくはこれらの混合物の縮合により得られるポリエーテルポリオール類;
ビスフェノールAやビスフェノールF等にエチレンオキサイド、プロピレンオキサイド等のアルキレンオキサイドを付加させてなるビスフェノール類等の芳香族ジオール類;
トリメチロールエタン、ポリトリメチロールエタン、トリメチロールプロパン、ポリトリメチロールプロパン、ペンタエリスリトール、ポリペンタエリスリトール、ソルビトール、マンニトール、アラビトール、キシリトール、ガラクチトール、グリセリン等の多価アルコールを原料の一部として用いて合成されたポリエチレンオキサイド、ポリプロピレンオキサイド、エチレンオキサイド/プロピレンオキサイドのブロック共重合体またはランダム共重合体、ポリテトラメチレングリコール、テトラメチレングリコールとネオペンチルグリコールとのブロック共重合体またはランダム共重合体等のポリエーテルポリオール類;
などの水酸基が2個以上のものを用いることができる。
シクロヘキサノール等の脂環族モノアルコール;
ベンジルアルコール、フルオレノール、等の芳香族モノアルコール;
フェノール、メトキノン等のフェノール類;
ヒドロキシル基以外の官能基を併有するモノアルコール化合物として、12−ヒドロキシステアリン酸等のヒドロキシル基含有カルボン酸化合物、グリシドールなどのヒドロキシル基含有エポキシ化合物、オキセタンアルコールなどのヒドロキシル基含有オキセタン化合物が挙げられる。その他、片末端メトキシ化ポリエチレングリコール、片末端メトキシ化ポリプロピレングリコール、モノアルコールを開始剤としたカプロラクトン付加重合物、などのオリゴマー型モノアルコールが挙げられる。
1,3−ビス(2−ヒドロキシエトキシ)ベンゼン、1,2−ビス(2−ヒドロキシエトキシ)ベンゼン、1,4−ビス(2−ヒドロキシエトキシ)ベンゼン、4,4’−メチレンジフェノール、4,4’−(2−ノルボルニリデン)ジフェノール、4,4’−ジヒドロキシビフェノール、o−,m−,およびp−ジヒドロキシベンゼン、4,4’−イソプロピリデンフェノール、1,2−インダンジオール、1,3−ナフタレンジオール、1,5−ナフタレンジオール、1,7−ナフタレンジオール、9,9’−ビス(4−ヒドロキシフェニル)フルオレン、9,9’−ビス(3−メチル−4−ヒドロキシフェニル)フルオレン等の芳香族ジオール類等を挙げることができる。その他、リン原子含有ジオール、硫黄原子含有ジオール、臭素原子含有ジオールなどが挙げられる。
ヘキサヒドロテレフタル酸、ヘキサヒドロイソフタル酸、ヘキサヒドロフタル酸、テトラヒドロフタル酸等の脂環族ジカルボン酸類;
シュウ酸、マロン酸、コハク酸、アジピン酸、セバチン酸、アゼライン酸、スベリン酸、マレイン酸、クロロマレイン酸、フマル酸、ドデカン二酸、ピメリン酸、シトラコン酸、グルタル酸、イタコン酸等の脂肪族ジカルボン酸類等が挙げられる。
ベンゾオキサジン化合物としては、Macromolecules,36,6010(2003)記載の「P−a」、「P−alp」、「P−ala」、「B−ala」、Macromolecules,34,7257(2001)記載の「P−appe」、「B−appe」、四国化成株式会社製「B−a型ベンゾオキサジン」、「F−a型ベンゾオキサジン」、「B−m型ベンゾオキサジン」などが挙げられる。
2−メチルイミダゾール、2−フェニルイミダゾール、2−ウンデシルイミダゾール、2−エチル−4−メチルイミダゾール、1−シアノエチル−2−メチルイミダゾール、2,4−ジシアノ−6−[2−メチルイミダゾリル−1]−エチル−S−トリアジン、2−エチル−4−メチルイミダゾールテトラフェニルボレート、等のイミダゾール類、およびその塩類;
1,5−ジアザビシクロ[5,4,0]−7−ウンデカン、1,5−ジアザビシクロ[4,3,0]−5−ノネン、1,4−ジアビシクロ[2,2,2,]オクタン、1,8−ジアザビシクロ[5.4.0]ウンデセン−7−テトラフェニルボレート等のジアザビシクロ化合物類;
トリブチルホスフィン、トリフェニルホスフィン、トリス(ジメトキシフェニル)ホスフィン、トリス(ヒドロキシプロピル)ホスフィン、トリス(シアノエチル)ホスフィン等のホスフィン類;
テトラフェニルホスホニウムテトラフェニルボレート、メチルトリブチルホスホニウムテトラフェニルボレート、メチルトリシアノエチルホスホニウムテトラフェニルボレート等のホスホニウム塩類;
その他、触媒的かつ自らも直接硬化反応に寄与する化合物として、ジシアンジアミド、カルボン酸ヒドラジド等が挙げられる。カルボン酸ヒドラジドとしては、コハク酸ヒドラジド、アジピン酸ヒドラジド等が挙げられる。
Mwの測定は東ソー株式会社製GPC(ゲルパーミエーションクロマトグラフィー)「HPC−8020」を用いた。GPCは溶媒(THF;テトラヒドロフラン)に溶解した物質をその分子サイズの差によって分離定量する液体クロマトグラフィーである。本発明における測定は、カラムに「LF−604」(昭和電工株式会社製:迅速分析用GPCカラム:6mmID×150mmサイズ)を直列に2本接続して用い、流量0.6ml/min、カラム温度40℃の条件で行い、重量平均分子量(Mw)の決定はポリスチレン換算で行った。
撹拌機、還流冷却管、窒素導入管、導入管、温度計を備えた4口フラスコに、ポリカーボネートジオール(クラレポリオール C−2090:株式会社クラレ製:3−メチル−1,5−ペンタンジオール/1,6−ヘキサンジオール=9/1(モル比)共重合ポリカーボネートジオール:水酸基価=56mgKOH/g、Mw=2000)292.1部、テトラヒドロ無水フタル酸(リカシッドTH:新日本理化株式会社製)44.9部、溶剤としてトルエン350部を仕込み、窒素気流下、攪拌しながら60℃まで昇温し、均一に溶解させた。続いてこのフラスコを110℃に昇温し、3時間反応させた。その後、40℃に冷却後、ビスフェノールA型エポキシ樹脂(YD−8125:東都化成株式会社製:エポキシ当量=175g/eq)62.9部、触媒としてトリフェニルホスフィン4部を添加して110℃に昇温し、8時間反応させた。室温まで冷却後、テトラヒドロ無水フタル酸11.8部を添加し、110℃で3時間反応させた。室温まで冷却後、トルエンで固形分が35%になるよう調整し、本発明のカルボキシル基含有変性エステル樹脂(A)溶液を得た。本製造例によって得たカルボキシル基含有変性エステル樹脂(A)の重量平均分子量は12600、実測による樹脂固形分の酸価は15.3mgKOH/gであった。
表1〜3に示す材料に代えた以外は製造例1と同様にして、本発明のカルボキシル基含有変性エステル樹脂(A)溶液を得た。
T−5652:旭化成ケミカルズ株式会社製、C5C6共重合ポリカーボネートジオール
UHC50−200:宇部興産株式会社製、1,6−ヘキサンジオール/カプロラクトン=5/5共重合ポリカーボネートジオール
UC−100:宇部興産株式会社製、1,4−シクロヘキサンジメタノールベースのポリカーボネートジオール
UM90(1/3):宇部興産株式会社製、1,4−シクロヘキサンジメタノール/1,6−ヘキサンジオール=1/3共重合ポリカーボネートジオール
UM90(1/1):宇部興産株式会社製、1,4−シクロヘキサンジメタノール/1,6−ヘキサンジオール=1/1共重合ポリカーボネートジオール
UM90(3/1):宇部興産株式会社製、1,4−シクロヘキサンジメタノール/1,6−ヘキサンジオール=3/1共重合ポリカーボネートジオール
PTG−2000SN:保土ヶ谷化学株式会社製、ポリテトラメチレングリコール
PTG−L2000:保土ヶ谷化学株式会社製、ポリテトラメチレングリコール(重量平均分子量約2000)
GI−2000:日本曹達株式会社製、水素添加型ポリブタジエングリコール(重量平均分子量約2100)
G−2000:日本曹達株式会社製、α,ω−ポリブタジエングリコール(重量平均分子量約1800)
Poly−ip:出光興産株式会社製、水酸基末端液状イソプレン(重量平均分子量約2500)
KF−6002:信越化学工業株式会社製、両末端カルビノール変性型シリコーンオイル(重量平均分子量約3000)
P−1041:株式会社クラレ製、3−メチル−1,5−ペンタンジオール/1,4−シクロヘキサンジカルボン酸共重合ポリエステルポリオール(重量平均分子量約1000)
P−2041:株式会社クラレ製、3−メチル−1,5−ペンタンジオール/1,4−シクロヘキサンジカルボン酸共重合ポリエステルポリオール(重量平均分子量約2000)
P−2010:株式会社クラレ製、脂肪族ポリエステルポリオール(重量平均分子量約2000)
C−590:株式会社クラレ製、3−メチル−1,5−ペンタンジオール/1,6−ヘキサンジオール=9/1(モル比)共重合ポリカーボネートジオール(重量平均分子量約600)
C−1090:株式会社クラレ製、3−メチル−1,5−ペンタンジオール/1,6−ヘキサンジオール=9/1(モル比)共重合ポリカーボネートジオール(重量平均分子量約1000)
TH:新日本理化株式会社製、テトラヒドロ無水フタル酸
HNA−100:新日本理化株式会社製、メチルビシクロ[2.2.1]ヘプタン−2,3−ジカルボン酸無水物
無水TMA:無水トリメリット酸
SA:新日本理化株式会社製、無水コハク酸
YD−8125:東都化成株式会社製、ビスフェノールA型エポキシ樹脂
EX−216L:ナガセケムテックス株式会社製、シクロヘキサンジメタノールジグリシジルエーテル
EX−214L:ナガセケムテックス株式会社製、1,4−ブタンジオールジグリシジルエーテル
EX−212L:ナガセケムテックス株式会社製、1,6−ヘキサンジオールジグリシジルエーテル
YX−8800:三菱化学株式会社製、ジヒドロキシアントラセン型エポキシ樹脂
YDF−8170C:東都化成株式会社製、ビスフェノールF型エポキシ樹脂
ZX−1059:東都化成株式会社製、ビスフェノール型エポキシ樹脂
BHPA:N,N−ビス(2−ヒドロキシプロピル)アニリン
DMBA:ジメチロールブタン酸
TMP:トリメチロールプロパン
1、6−HD:1,6−ヘキサンジオール
製造例1で得られたカルボキシル基含有変性エステル樹脂(A)溶液の固形分100部に対して、化合物(B)として、多官能グリシジルエーテル型エポキシ樹脂(三菱化学社製「エピコート1031S」)20部、および、熱硬化助剤(C)としてケミタイトPZ(株式会社日本触媒製、多官能アジリジン化合物)1部を混合し、熱硬化性樹脂組成物を得た。この熱硬化性樹脂組成物を剥離処理されたポリエステルフィルム上に、乾燥後の膜厚が30μmとなるように均一に塗工して乾燥させ、接着剤層を設けた。次に、剥離処理された別のポリエステルフィルムを接着剤層側にラミネートし、両面保護フィルム付きの接着シートを得た。
実施例1で使用した製造例1のカルボキシル基含有変性エステル樹脂(A)溶液を、製造例2〜27で得られたカルボキシル基含有変性エステル樹脂(A)溶液にそれぞれ代えた以外は、実施例1と同様にして、両面保護フィルム付きの接着シートを作成した。
製造例28で得られたカルボキシル基含有変性エステル樹脂(A)溶液の固形分100部に対して、化合物(B)として、多官能グリシジルエーテル型エポキシ樹脂(三菱化学社製「エピコート1031S」)18部、および、熱硬化助剤(C)としてジシアンジアミド1部を混合し、熱硬化性樹脂組成物を得た。この熱硬化性樹脂組成物を剥離処理されたポリエステルフィルム上に、乾燥後の膜厚が30μmとなるように均一に塗工して乾燥させ、接着剤層を設けた。次に、剥離処理された別のポリエステルフィルムを接着剤層側にラミネートし、両面保護フィルム付きの接着シートを得た。
実施例28で使用した製造例28のカルボキシル基含有変性エステル樹脂(A)溶液を、製造例29〜36で得られたカルボキシル基含有変性エステル樹脂(A)溶液にそれぞれ代えた以外は、実施例1と同様にして、両面保護フィルム付きの接着シートを作成した。
表4に示した組成で熱硬化性樹脂組成物を得た以外は、実施例1と同様にして、両面保護フィルム付きの接着シートを作成した。
EOCN−102S:日本化薬株式会社製、クレゾールノボラック型エポキシ樹脂
EPPN−201L:日本化薬株式会社製、フェノールノボラック型エポキシ樹脂
YH434L:東都化成株式会社製、四官能ポリグリシジルアミン
オンコート1040:ナガセケムテックス株式会社製、フルオレン型多官能エポキシ樹脂
BL3175:住化バイエルウレタン株式会社製、イソシアヌレート型ブロックイソシアネート
B80T:旭化成ケミカルズ株式会社製、ブロックイソシアネート
DICY:ジシアンジアミド
ケミタイトPZ:株式会社日本触媒製、多官能アジリジン化合物
リカシッドTMTA−C:新日本理化株式会社製、多官能酸無水物
アロンオキセタンOXT−121:東亞合成株式会社製、1,4−ビス{[(3−エチルオキセタン−3−イル)メトキシ]メチル}オキセタン
B−a:四国化成株式会社製、ベンゾオキサジン化合物
カルボジライトV−07:日清紡株式会社製、ポリカルボジイミド化合物
ZISNET DB:三協化成株式会社製、2−ジブチルアミノ−4,6−ジメルカプト−s−トリアジン
TD−2131:DIC株式会社製、フェノールノボラック樹脂
BMI−2300:大和化成工業株式会社製、ポリフェニルメタンマレイミド化合物
実施例1のカルボキシル基含有変性エステル樹脂(A)溶液を、比較製造例1〜9で得られた樹脂溶液にそれぞれ代えた以外は、実施例1と同様にして、両面保護フィルム付きの接着シートを作成した。
保護フィルムを除去した、65mm×65mmの大きさの接着シートを、厚さが75μmのポリイミドフィルム[東レ・デュポン(株)製「カプトン300H」]と厚さが45μmの銅張積層板との間に挟み、80℃でラミネートし、続いて160℃、1.0MPaの条件で1時間圧着処理を行った。さらに、この試験片を160℃で2時間熱硬化させ、評価用試験片を作成した。この試験片について、圧着処理前と熱硬化後との接着剤層の面積の差を測定し、これをはみ出し面積として加工安定性を評価した。この加工安定性は、圧着処理時に接着層が熱によって軟化し、回路基板の位置ズレや配線間の接触を引き起こす度合いを評価するものであり、結果を次の基準で判断した。
◎・・・「はみ出し面積 ≦ 100mm2」
○・・・「100mm2 < はみ出し面積 ≦ 250mm2」
△・・・「250mm2 < はみ出し面積 ≦ 500mm2」
×・・・「500mm2 < はみ出し面積」
加工安定性の評価で作成した試験片を幅10mm、長さ65mmに切り出し、23℃相対湿度50%の雰囲気下で、引っ張り速度300mm/minでTピール剥離試験を行い、接着強度(N/cm)を測定した。この試験は、常温使用時における接着層の接着強度を評価するものであり、結果を次の基準で判断した。
◎・・・「18(N/cm) < 接着強度」
○・・・「12(N/cm) < 接着強度 ≦ 18(N/cm)」
△・・・「8(N/cm) < 接着強度 ≦ 12(N/cm)」
×・・・「接着強度 ≦ 8(N/cm)」
実施例および比較例で作成した両面保護フィルム付き接着シートを、40℃で3ヶ月間加熱保存した後、上記(1)の条件でラミネート、圧着処理および熱硬化を施し、接着強度を上記(2)と同じ方法で評価し、加熱保存していない接着シートで得られる接着強度と比較した。この試験は、未硬化状態の接着層の経時安定性を、加熱保存の有無による接着強度の差異をもって評価するものであり、経時安定性の良好なものほど未硬化の状態が安定で、加熱促進を施した場合でも接着強度の低下は少なく、経時安定性の悪いものほど、未硬化の状態が不安定で、加熱促進によって硬化反応が進行してしまい、加熱促進を施さない場合に比べて接着強度が大きく低下する。これらの評価結果を次の基準で判断した。
◎・・・「加熱促進により接着強度が全く変化しない」
○・・・「加熱促進により接着強度がほとんど変化しない」
△・・・「加熱促進により接着強度がやや低下した」
×・・・「加熱促進により接着強度が著しく低下した」
上記(2)と同様に、幅10mm、長さ65mmに切り出した試験片を、260℃の溶融半田に、ポリイミドフィルム面を接触させて1分間浮かべた。その後、試験片の外観を目視で観察し、接着剤層の発泡、浮き、剥がれ等の接着異常の有無を評価した。この試験は、半田接触時における接着層の熱安定性を、外観で評価するものであり、耐熱性の良好なものは、半田処理の前後で外観が変化しないのに対して、耐熱性の悪いものは、半田処理後に発泡や剥がれが発生する。これらの評価結果を次の基準で判断した。
◎・・・「外観変化無し」
○・・・「小さな発泡がわずかに観察される」
△・・・「発泡が観察される」
×・・・「激しい発泡や剥がれが観察される」
上記(4)の半田浴耐性評価後の試験片について、上記(2)と同様の方法で接着強度を測定し、半田処理前の接着強度と半田処理後の接着強度とを比較した。この試験は、半田接触時における接着層の熱安定性を、半田処理前後における接着強度の変化で評価するものであり、耐熱性の良好なものは、半田処理の前後で接着強度が変化しないのに対して、耐熱性の悪いものは、半田処理後に接着強度が著しく低下する。これらの評価結果を次の基準で判断した。
◎・・・「接着強度が全く変化しない」
○・・・「接着強度がほとんど変化しない」
△・・・「接着強度がやや低下した」
×・・・「接着強度が著しく低下した」
上記(2)と同様に、幅10mm、長さ65mmに切り出した試験片を、40℃、相対湿度90%の雰囲気で96時間放置して加湿させた後、260℃の溶融半田に、ポリイミドフィルム面を接触させて1分間浮かべた。その後、試験片の外観を目視で観察し、接着剤層の発泡、浮き、剥がれ等の接着異常の有無を評価した。この試験は、加湿させた状態での半田接触時における接着層の熱安定性を、外観で評価するものであり、耐湿熱性の良好なものは、外観が変化しないのに対して、耐湿熱性の悪いものは、半田処理後に発泡や剥がれが発生する。これらの評価結果を次の基準で判断した。
◎・・・「外観変化全く無し」
○・・・「外観変化ほとんど無し」
△・・・「発泡が観察される」
×・・・「激しい発泡や剥がれが観察される」
保護フィルムを除去した、65mm×65mmの大きさの接着シートを、厚さが25μmのポリイミドフィルム[東レ・デュポン(株)製「カプトン100H」]とポリイミド上に銅回路が形成された櫛型パターン(導体パターン幅/スペース幅=50μm/50μm)印刷回路基板との間に挟み、80℃でラミネートし、続いて160℃、1.0MPaの条件で1時間圧着処理を行った。さらに、この試験片を160℃で2時間熱硬化させ、評価用試験片を作成した。この試験片の導体回路に、温度130℃、相対湿度85%の雰囲気下で直流電圧50Vを連続的に100時間加え、100時間後の導体間の絶縁抵抗値を測定した。評価基準は以下の通りである。
◎・・・絶縁抵抗値108Ω以上
○・・・絶縁抵抗値107以上108Ω未満
△・・・絶縁抵抗値106以上107Ω未満
×・・・絶縁抵抗値106Ω未満
熱硬化性樹脂組成物を、厚さが75μmのポリイミドフィルム[東レ・デュポン(株)製「カプトン300H」]上に、乾燥後の膜厚が30μmになるように均一に塗工して乾燥させ、さらに、この試験片を160℃で1時間熱硬化させ、評価用試験片を作成した。この試験片上に弱活性ロジン系フラックス(日本アルファメタルズ株式会社製、商品名:RM−615)を数滴垂らした後、260℃のオーブンで3分間熱処理した。試験片をオーブンから取り出し、フラックスをイソプロピルアルコールで拭き取った後、ポリイミド上の硬化膜の厚さによって下記のように判断した。実用上問題ないものは○である。
〇・・・膜厚変化が5μm未満
△・・・膜厚変化が5〜10μm
×・・・膜厚変化が10μmよりも大きい
評価の結果を下記表5に示す。
実施例と比較例をみてわかるとおり、実施例では、脂環式多塩基酸無水物および芳香族多塩基酸無水物から選ばれる少なくとも1種である酸無水物基含有化合物(b)を使用して樹脂を合成しており、全ての物性において良好な結果を示した。さらには、熱硬化助剤(C)を加えることにより、接着強度、絶縁信頼性等を低下させないで加工性や加湿半田耐性、半田後の接着強度を向上することができた。これらは、エステル結合基が嵩高い置換基で保護されたことによる耐加水分解性と熱硬化助剤(C)との相乗効果であることが考えられる。
Claims (7)
- カルボキシル基含有変性エステル樹脂(A)、エポキシ基含有化合物、イソシアネート基含有化合物、およびブロック化イソシアネート基含有化合物からなる群より選ばれる少なくとも一種である化合物(B)、およびアジリジン化合物、カルボジイミド基含有化合物、ベンゾオキサジン化合物、フェノール樹脂、イミダゾール類、およびジシアンジアミドからなる群より選ばれる少なくとも1種である熱硬化助剤(C)を含む熱硬化性樹脂組成物であって、
カルボキシル基含有変性エステル樹脂(A)が、
ポリオール化合物(a)と、脂環式多塩基酸無水物および芳香族多塩基酸無水物から選ばれる少なくとも1種である酸無水物基含有化合物(b)とを反応させてカルボキシル基含有エステル樹脂(c)を生成し、
前記カルボキシル基含有エステル樹脂(c)と1分子中に少なくとも2個のエポキシ基を有するエポキシ化合物(d)とを反応させて側鎖ヒドロキシル基含有変性エステル樹脂(e)を生成し、さらに、側鎖ヒドロキシル基含有変性エステル樹脂(e)に脂環式多塩基酸無水物および芳香族多塩基酸無水物から選ばれる少なくとも1種である酸無水物基含有化合物(b)を反応させてなることを特徴とする熱硬化性樹脂組成物。 - ポリオール化合物(a)が、ポリエステルポリオール、ポリカーボネートポリオール、ポリエーテルポリオール、ポリブタジエンポリオール、およびポリシロキサンポリオールからなる群より選ばれる少なくとも1種の化合物である請求項1記載の熱硬化性樹脂組成物。
- 酸無水物基含有化合物(b)が、メチルテトラヒドロ無水フタル酸、テトラヒドロ無水フタル酸、ヘキサヒドロ無水フタル酸、メチルヘキサヒドロ無水フタル酸、無水ナジック酸、メチル無水ナジック酸、水素化メチル無水ナジック酸、スチルエンドスチレンテトラヒドロ無水フタル酸、3,6−エンドメチレンテトラヒドロ無水フタル酸、メチルエンドメチレンテトラヒドロ無水フタル酸、トリアルキルテトラヒドロ無水フタル酸、無水フタル酸、テトラブロモ無水フタル酸、無水トリメリット酸、および無水ピロメリット酸からなる群より選ばれる少なくとも1種の化合物である請求項1または2記載の熱硬化性樹脂組成物。
- カルボキシル基含有変性エステル樹脂(A)の酸価が、1〜100mgKOH/gである請求項1〜3いずれか記載の熱硬化性樹脂組成物。
- カルボキシル基含有変性エステル樹脂(A)の重量平均分子量が5000〜500000である請求項1〜4いずれか記載の熱硬化性樹脂組成物。
- 請求項1〜5いずれか記載の熱硬化性樹脂組成物を加熱により硬化させて得られる硬化物。
- 請求項6に記載の硬化物からなる層を有することを特徴とするプリント配線板。
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JP6409760B2 (ja) * | 2014-12-11 | 2018-10-24 | 東洋インキScホールディングス株式会社 | プリント配線板の製造方法 |
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