JP2010237578A - 光硬化性樹脂組成物 - Google Patents
光硬化性樹脂組成物 Download PDFInfo
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- JP2010237578A JP2010237578A JP2009087374A JP2009087374A JP2010237578A JP 2010237578 A JP2010237578 A JP 2010237578A JP 2009087374 A JP2009087374 A JP 2009087374A JP 2009087374 A JP2009087374 A JP 2009087374A JP 2010237578 A JP2010237578 A JP 2010237578A
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- 125000000217 alkyl group Chemical group 0.000 claims abstract description 40
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 24
- 239000003999 initiator Substances 0.000 claims abstract description 20
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- 125000000524 functional group Chemical group 0.000 claims abstract description 5
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Abstract
【解決手段】一般式(I)で示される水酸基含有樹脂と、カルボキシル基含有樹脂と、光重合開始剤と、を含有することを特徴とするアルカリ現像性の光硬化性樹脂組成物。
(式中、R1は水素原子、炭素数1〜20の有機基、R2は、炭素数1〜10のアルキル基、炭素数1〜10のアルキレン基、及びフェニレン基よりなる群から選ばれる少なくとも1種の官能基、R3は、水素原子又は炭素数1〜4のアルキル基、R4は水素原子又は炭素数1〜4のアルキル基、pは1〜5の整数、qは、2以上の整数、mは1〜4の整数、nは1〜10の整数を表わす。)
【選択図】なし
Description
このような構成により、優れた指触乾燥性、現像性、及びスルーホール現像性を得ることができるとともに、その硬化物において、従来と同等以上のはんだ耐熱性、耐無電解金めっき性、電気特性を得ることが可能となる。
そして、水酸基を有する、一般式(I)で示される構造を含む感光性樹脂を用いている点に特徴がある。
一般式(II)で表される基を有するオキシムエステル系光重合開始剤としては、式(V)で表される2−(アセチルオキシイミノメチル)チオキサンテン−9−オン、一般式(VI)で表される化合物、及び一般式(VII)で表される化合物が好ましい。
これらオキシムエステル系光重合開始剤の中でも、一般式(V)で表される2−(アセチルオキシイミノメチル)チオキサンテン−9−オン、及び一般式(VI)で表される化合物がより好ましい。市販品としては、チバ・スペシャルティ・ケミカルズ社製のCGI−325、イルガキュアーOXE01、イルガキュアーOXE02、ADEKA社製のN−1919等が挙げられる。これらのオキシムエステル系光重合開始剤は、単独で又は2種以上を組み合わせて用いることができる。
赤色着色剤としては、モノアゾ系、ジズアゾ系、アゾレーキ系、ベンズイミダゾロン系、ペリレン系、ジケトピロロピロール系、縮合アゾ系、アントラキノン系、キナクリドン系などがあり、具体的には以下のものが挙げられる。
青色着色剤としては、フタロシアニン系、アントラキノン系があり、顔料系は、ピグメント(Pigment)に分類されている化合物、具体的には、以下のようなカラーインデックス(C.I.;ザ ソサイエティ オブ ダイヤーズ アンド カラリスツ(The Society of Dyers and Colourists)発行)番号が付されている、:Pigment Blue 15、Pigment Blue 15:1、Pigment Blue 15:2、Pigment Blue 15:3、Pigment Blue 15:4、Pigment Blue 15:6、Pigment Blue 16、Pigment Blue 60等を挙げることができる。
緑色着色剤としては、同様にフタロシアニン系、アントラキノン系、ペリレン系があり、具体的にはPigment Green 7、Pigment Green 36、Solvent Green 3、Solvent Green 5、Solvent Green 20、Solvent Green 28等を使用することができる。これら以外にも、金属置換もしくは無置換のフタロシアニン化合物も使用することができる。
黄色着色剤としては、モノアゾ系、ジスアゾ系、縮合アゾ系、ベンズイミダゾロン系、イソインドリノン系、アントラキノン系等があり、具体的には以下のものが挙げられる。
このような分子中に2個以上のエチレン性不飽和基を有する化合物の配合量は、カルボキシル基含有樹脂100質量部に対して、5〜100質量部であることが好ましい。配合量が5質量部未満の場合、光硬化性が低下し、活性エネルギー線照射後のアルカリ現像により、パターン形成が困難となる。一方、100質量部を超えた場合、アルカリ水溶液に対する溶解性が低下して、塗膜が脆くなる。より好ましくは、1〜70質量部である。
温度計、窒素導入装置兼アルキレンオキシド導入装置及び撹拌装置を備えたオートクレーブに、ノボラック型フェノール樹脂(昭和高分子株式会社製:BRG−558、水酸基当量104)104部、50%水酸化ナトリウム水溶液2.6部、トルエン/メチルイソブチルケトン(質量比=2/1)100部を仕込み、撹拌しつつ系内を窒素置換し、次に加熱昇温し、150℃、8kg/cm2でプロピレンオキシド60部を徐々に導入し反応させた。ゲージ圧0.0kg/cm2となるまで約4時間反応を続けた後、室温まで冷却した。この反応溶液に3.3部の36%塩酸水溶液を添加混合し、水酸化ナトリウムを中和した。この中和反応生成物をトルエンで希釈し、3回水洗し、エバポレーターにて脱溶剤して、水酸基当量が164g/eq.のノボラック型フェノール樹脂のアルキレンオキシド付加物を得た。これは、水酸基1当量当りアルキレンオキシドが平均1モル付加しているものであった。
温度計、窒素導入装置兼アルキレンオキシド導入装置及び撹拌装置を備えたオートクレーブに、ノボラック型フェノール樹脂(昭和高分子株式会社製:BRG−558、水酸基当量104)104部、50%水酸化ナトリウム水溶液2.6部、トルエン/メチルイソブチルケトン(質量比=2/1)100部を仕込み、撹拌しつつ系内を窒素置換し、次に加熱昇温し、150℃、8kg/cm2でプロピレンオキシド120部を徐々に導入し反応させた。ゲージ圧0.0kg/cm2となるまで約4時間反応を続けた後、室温まで冷却した。この反応溶液に3.3部の36%塩酸水溶液を添加混合し、水酸化ナトリウムを中和した。この中和反応生成物をトルエンで希釈し、3回水洗し、エバポレーターにて脱溶剤して、水酸基当量が224g/eq.のノボラック型フェノール樹脂のアルキレンオキシド付加物を得た。これは、水酸基1当量当りアルキレンオキシドが平均2モル付加しているものであった。
温度計、窒素導入装置兼アルキレンオキシド導入装置及び撹拌装置を備えたオートクレーブに、4,4‘−ビフェニルジイルジメチレン−フェノール樹脂(水酸基当量219)219部、50%水酸化ナトリウム水溶液2.6部、トルエン/メチルイソブチルケトン(質量比=2/1)100部を仕込み、撹拌しつつ系内を窒素置換し、次に加熱昇温し、150℃、8kg/cm2でプロピレンオキシド60部を徐々に導入し反応させた。ゲージ圧0.0kg/cm2となるまで約4時間反応を続けた後、室温まで冷却した。この反応溶液に3.3部の36%塩酸水溶液を添加混合し、水酸化ナトリウムを中和した。この中和反応生成物をトルエンで希釈し、3回水洗し、エバポレーターにて脱溶剤して、水酸基当量が279g/eq.の4,4‘−ビフェニルジイルジメチレン−フェノール樹脂のアルキレンオキシド付加物を得た。これは、水酸基1当量当りアルキレンオキシドが平均1モル付加しているものであった。
温度計、窒素導入装置兼アルキレンオキシド導入装置及び撹拌装置を備えたオートクレーブに、3,3’,5,5’−テトラメチル−4,4’−ビフェノール(水酸基当量121)121部、50%水酸化ナトリウム水溶液2.6部、トルエン/メチルイソブチルケトン(質量比=2/1)100部を仕込み、撹拌しつつ系内を窒素置換し、次に加熱昇温し、150℃、8kg/cm2でプロピレンオキシド60部を徐々に導入し反応させた。ゲージ圧0.0kg/cm2となるまで約4時間反応を続けた後、室温まで冷却した。この反応溶液に3.3部の36%塩酸水溶液を添加混合し、水酸化ナトリウムを中和した。この中和反応生成物をトルエンで希釈し、3回水洗し、エバポレーターにて脱溶剤して、水酸基当量が181g/eq.のノボラック型フェノール樹脂のアルキレンオキシド付加物を得た。これは、水酸基1当量当りアルキレンオキシドが平均1モル付加しているものであった。
温度計、窒素導入装置兼アルキレンオキシド導入装置及び撹拌装置を備えたオートクレーブに、ノボラック型フェノール樹脂(昭和高分子株式会社製:BRG−558、水酸基当量104)104部、50%水酸化ナトリウム水溶液2.6部、トルエン/メチルイソブチルケトン(質量比=2/1)100部を仕込み、撹拌しつつ系内を窒素置換し、次に加熱昇温し、150℃、8kg/cm2でエチレンオキシド50部を徐々に導入し反応させた。ゲージ圧0.0kg/cm2となるまで約4時間反応を続けた後、室温まで冷却した。この反応溶液に3.3部の36%塩酸水溶液を添加混合し、水酸化ナトリウムを中和した。この中和反応生成物をトルエンで希釈し、3回水洗し、エバポレーターにて脱溶剤して、水酸基当量が154g/eq.のノボラック型フェノール樹脂のアルキレンオキシド付加物を得た。これは、水酸基1当量当りアルキレンオキシドが平均1モル付加しているものであった。
温度計、窒素導入装置兼アルキレンオキシド導入装置及び撹拌装置を備えたオートクレーブに、単官能フェノール化合物(水酸基当量94)94部、50%水酸化ナトリウム水溶液2.6部、トルエン/メチルイソブチルケトン(質量比=2/1)100部を仕込み、撹拌しつつ系内を窒素置換し、次に加熱昇温し、150℃、8kg/cm2でエチレンオキシド50部を徐々に導入し反応させた。ゲージ圧0.0kg/cm2となるまで約4時間反応を続けた後、室温まで冷却した。この反応溶液に3.3部の36%塩酸水溶液を添加混合し、水酸化ナトリウムを中和した。この中和反応生成物をトルエンで希釈し、3回水洗し、エバポレーターにて脱溶剤して、水酸基当量が138g/eq.のフェノール化合物のアルキレンオキシド付加物を得た。これは、水酸基1当量当りアルキレンオキシドが平均1モル付加しているものであった。
ジエチレングリコールモノエチルエーテルアセテート600gにオルソクレゾールノボラック型エポキシ樹脂〔大日本インキ化学工業株式会社製、EPICLON N−695、軟化点95℃、エポキシ当量214、平均官能基数7.6〕1070g、アクリル酸360g、及びハイドロキノン1.5gを仕込み、100℃に加熱攪拌し、均一溶解した。次いで、トリフェニルホスフィン4.3gを仕込み、110℃に加熱して2時間反応後、120℃に昇温してさらに12時間反応を行った。得られた反応液に芳香族系炭化水素(ソルベッソ150)415g、テトラヒドロ無水フタル酸456.0gを仕込み、110℃で4時間反応を行い、冷却後、固形分酸価89mgKOH/g、固形分65%の樹脂溶液を得た。以下、このカルボキシル基含有樹脂の溶液を、B−1ワニスと称す。
温度計、窒素導入装置兼アルキレンオキシド導入装置及び撹拌装置を備えたオートクレーブに、ノボラック型クレゾール樹脂(昭和高分子(株)製、商品名「ショーノールCRG951」、OH当量:119.4)119.4g、水酸化カリウム1.19g及びトルエン119.4gを仕込み、撹拌しつつ系内を窒素置換し、加熱昇温した。次に、プロピレンオキシド63.8gを徐々に滴下し、125〜132℃、0〜4.8kg/cm2で16時間反応させた。その後、室温まで冷却し、この反応溶液に89%リン酸1.56gを添加混合して水酸化カリウムを中和し、不揮発分62.1%、水酸基価が182.2g/eq.であるノボラック型クレゾール樹脂のプロピレンオキシド反応溶液を得た。これは、フェノール性水酸基1当量当りアルキレンオキシドが平均1.08モル付加しているものであった。得られたノボラック型クレゾール樹脂のアルキレンオキシド反応溶液293.0g、アクリル酸43.2g、メタンスルホン酸11.53g、メチルハイドロキノン0.18g及びトルエン252.9gを、撹拌機、温度計及び空気吹き込み管を備えた反応器に仕込み、空気を10ml/分の速度で吹き込み、撹拌しながら、110℃で12時間反応させた。反応により生成した水は、トルエンとの共沸混合物として、12.6gの水が留出した。その後、室温まで冷却し、得られた反応溶液を15%水酸化ナトリウム水溶液35.35gで中和し、次いで水洗した。その後、エバポレーターにてトルエンをジエチレングリコールモノエチルエーテルアセテート118.1gで置換しつつ留去し、ノボラック型アクリレート樹脂溶液を得た。次に、得られたノボラック型アクリレート樹脂溶液332.5g及びトリフェニルホスフィン1.22gを、撹拌器、温度計及び空気吹き込み管を備えた反応器に仕込み、空気を10ml/分の速度で吹き込み、撹拌しながら、テトラヒドロフタル酸無水物60.8gを徐々に加え、95〜101℃で6時間反応させた。固形物の酸価88mgKOH/g、不揮発分71%のカルボキシル基含有感光性樹脂を得た。以下、この反応溶液をB−2ワニスと称す
(実施例1〜11及び比較例1〜5)
このようにして調製されたA−1〜A−6ワニス、B−1、B−2ワニスを用い、表1に示す種々の成分とともに表1に示す割合(質量部)にて配合した。そして、攪拌機にて予備混合した後、3本ロールミルで混練し、ソルダーレジスト用光硬化性樹脂組成物を調製した。ここで、得られた光硬化性樹脂組成物の分散度をエリクセン社製グラインドメータによる粒度測定にて評価したところ、15μm以下であった。
*2:ノボラック型フェノール樹脂(BRG−558:昭和高分子社製)
*3:ZFR−1124(日本化薬(株)製)
*4:2-メチル-1-(4-メチルチオフェニル)-2-モルフォリノプロパン-1-オン(イルガキュアー907:チバ・スペシャルティー・ケミカルズ社製)
*5:エタノン,1−[9−エチル−6−(2−メチルベンゾイル)−9H−カルバゾール−3−イル]1,1−(O-アセチルオキシム)(OXE−02:チバ・スペシャルティー・ケミカルズ社製)
*6:ブロックイソシアネート(旭化成ケミカルズ社製)
*7:フェノールノボラック型エポキシ樹脂(DEN438:ダウケミカル社製)
*8:ビキシレノール型エポキシ樹脂(YX-4000:ジャパンエポキシレジン(株)製)
*9:C.I.Pigment Blue 15:3
*10:C.I.Pigment Yellow 147
*11:酸化防止剤(チバ・スペシャリティー・ケミカルズ社製)
*12:B-30(堺化学(株)製)
*13:ジプロピレングリコールモノメチルエーテル
*14:ジペンタエリスリトールヘキサアクリレート(日本化薬(株)製)
*15:メチル化メラミン樹脂((株)三和ケミカル製)
〈最適露光量〉
膜厚35μmの銅層の回路パターンが形成された基板をバフロール研磨後、水洗し、乾燥した後、実施例及び比較例の光硬化性樹脂組成物をスクリーン印刷法により全面に塗布し、80℃の熱風循環式乾燥炉で60分間乾燥させた。乾燥後、高圧水銀灯(ショートアークランプ)搭載の露光装置を用いてステップタブレット(Kodak No.2)を介して露光し、現像(30℃、0.2MPa、1wt%Na2CO3水溶液)を60秒で行った際、残存するステップタブレットのパターンが7段の時を最適露光量とした。
実施例及び比較例の光硬化性樹脂組成物を、銅ベタ基板上にスクリーン印刷法により、約25μmになるように塗布し、80℃の熱風循環式乾燥炉で30分間乾燥させた。乾燥後、1質量%炭酸ナトリウム水溶液によって現像を行い、乾燥塗膜が除去されるまでの時間をストップウォッチにより計測した。
1.0mmtの銅張積層板にφ200μmドリルで穴を開け、定法によりスルーホールメッキを行い、実測値約φ150μmのスルーホールを400穴形成した基板を作製した。その基板に実施例及び比較例の光硬化性樹脂組成物をスクリーン印刷法で2回印刷し、光硬化性樹脂組成物を充填させることで穴埋めを行った。さらに、80℃の熱風循環式乾燥炉で30分間乾燥させ、室温まで冷却した。その後、30℃の1質量%炭酸ナトリウム水溶液を用い、スプレー圧0.2MPaの条件で120秒間現像を行い、以下の基準にて評価した。
◎:1回〜2回現像を行うことで100%スルーホールの現像可能
○:3回〜5回現像を行うことで100%スルーホールの現像可能
△:3回〜5回現像を行うことで50〜99%スルーホのール現像可能
×:5回現像を行ってもスルーホールの現像可能率50%以下
実施例及び比較例の光硬化性樹脂組成物を、それぞれパターン形成された銅箔基板上にスクリーン印刷で全面塗布し、80℃の熱風循環式乾燥炉で30分間乾燥させ、室温まで放冷した。この基板にPETフィルムを押し当て、その後、ネガフィルムを剥がしたときのフィルムの張り付き状態を評価した。
◎:フィルムを剥がすときに、全く抵抗が無く、塗膜に跡が残らない
○:フィルムを剥がす時に、全く抵抗が無いが、塗膜に跡が少しついている
△:フィルムを剥がす時に、僅かに抵抗があり、塗膜に跡が少しついている
×:フィルムを剥がす時に、抵抗があり、塗膜にはっきり跡がついている
ライン/スペースが300/300μm、銅厚35μmの回路パターン基板をバフロール研磨後、水洗し、乾燥した後、実施例及び比較例の光硬化性樹脂組成物をスクリーン印刷法により塗布し、80℃の熱風循環式乾燥炉で30分間乾燥させた。乾燥後、高圧水銀灯(ショートアークランプ)搭載の露光装置を用いて露光した。露光パターンはスペース部に20/30/40/50/60/70/80/90/100μmのラインを描画させるガラス乾板を使用した。露光量は光硬化性樹脂組成物の最適露光量となるように活性エネルギー線を照射した。露光後、30℃の1wt%Na2CO3水溶液によって現像を行ってパターンを描き、150℃で60分の熱硬化をすることにより硬化塗膜を得た。
予め水洗・乾燥を行なったPTFE(ポリテトラフルオロエチレン)板に、各組成例及び比較組成例の組成物をスクリーン印刷法で塗布し、熱風循環式乾燥炉で80℃で30分乾燥させた。これを室温まで冷却した後、適正露光量で露光し、30℃の1wt%Na2CO3水溶液をスプレー圧2kg/cm2の条件で60秒間現像を行った。この基板を、UVコンベア炉にて積算露光量1000mJ/cm2の条件で紫外線照射した後、熱風循環式乾燥炉で硬化を150℃で60分間行なった。これを室温まで冷却した後、PTFE板から硬化塗膜をはがし、評価サンプルを得た。
予め水洗・乾燥を行なったカプトン材(厚さ25μm)に、各実施例及び比較例の組成物をスクリーン印刷法で塗布し、熱風循環式乾燥炉で80℃で30分乾燥させた。これを室温まで冷却した後、高圧水銀灯(ショートアークランプ)搭載の露光装置を用いて適正露光量で露光し、30℃の1wt%Na2CO3水溶液をスプレー圧2kg/cm2の条件で60秒間現像を行った。この基板を、UVコンベア炉にて積算露光量1000mJ/cm2の条件で紫外線照射した後、150℃で60分加熱して硬化し、耐折性試験及び柔軟性試験用の評価サンプルを得た。
○:10g未満
△:10〜30g未満
×:30g以上
各実施例及び比較例の光硬化性樹脂組成物を、スクリーン印刷で乾燥後の膜厚が20μmになるように、パターン形成された銅箔基板上に全面塗布し、80℃で30分乾燥し、室温まで放冷する。この基板に高圧水銀灯(ショートアークランプ)搭載の露光装置を用いて最適露光量でソルダーレジストパターンを露光し、30℃の1wt%Na2CO3水溶液をスプレー圧2kg/cm2の条件で60秒間現像を行い、レジストパターンを得た。この基板を、UVコンベア炉にて積算露光量1000mJ/cm2の条件で紫外線照射した後、150℃で60分加熱して硬化した。得られたプリント基板(評価基板)に対して、以下のように特性を評価した。
ロジン系フラックスを塗布した評価基板を、予め260℃に設定したはんだ槽に浸漬し、変性アルコールでフラックスを洗浄した後、目視によるレジスト層の膨れ・剥がれについて評価した。判定基準は以下のとおりである。
◎:10秒間浸漬を6回以上繰り返しても剥がれが認められない
○:10秒間浸漬を3回以上繰り返しても剥がれが認められない
△:10秒間浸漬を3回以上繰り返すと少し剥がれる
×:10秒間浸漬を3回以内にレジスト層に膨れ、剥がれがある
市販品の無電解ニッケルめっき浴及び無電解金めっき浴を用いて、ニッケル0.5μm、金0.03μmの条件でめっきを行い、テープピーリングにより、レジスト層の剥がれの有無やめっきのしみ込みの有無を評価した後、テープピーリングによりレジスト層の剥がれの有無を評価した。判定基準は以下のとおりである。
◎:染み込み、剥がれが見られない
○:めっき後に少し染み込みが確認されるが、テープピール後は剥がれない
△:めっき後にほんの僅かしみ込みが見られ、テープピール後に剥がれも見られる
×:めっき後に剥がれが有る
銅箔基板に代えてライン/スペース=50/50μmのクシ型電極パターンを用い、同様にして評価基板を作製した。このクシ型電極にDC10Vのバイアス電圧を印加し、130℃、85%R.H.にて100時間後の絶縁抵抗値を槽内で測定した。測定電圧はDC10Vで行った。
評価基板を10wt%NaOH水溶液に50℃で30分間浸漬し、染み込みや塗膜の溶け出し、さらにテープビールによる剥がれを確認した。判定基準は以下のとおりである。
○:染み込み、溶け出し、剥がれなし
△:染み込み、溶け出し、もしくは剥がれが少し確認される
×:染み込み、溶け出し、もしくは剥がれが大きく確認される
実施例4及び比較例4の光硬化性樹脂組成物を、それぞれメチルエチルケトンで適宜希釈した後、アプリケーターを用いて、乾燥後の膜厚が20μmになるようにPETフィルム(東レ株式会社製 FB−50:16μm)に塗布し、80℃で30分乾燥させドライフィルムを得た。
回路形成された基板をバフ研磨した後、得られたドライフィルムを真空ラミネーター(名機製作所製 MVLP−500)を用いて加圧度:0.8MPa、70℃、1分、真空度:133.3Paの条件で加熱ラミネートして、未露光のソルダーレジスト層を有する基板(未露光の基板)を得た。
Claims (15)
- 前記水酸基含有樹脂は、1分子中に2つ以上のフェノール性水酸基を有する化合物に、環状エーテル化合物又は環状カーボネート化合物を反応させた化合物であることを特徴とする請求項1に記載の光硬化性樹脂組成物。
- 前記1分子中に2つ以上のフェノール性水酸基を有する化合物の軟化点は、室温以上であることを特徴とする請求項2に記載の光硬化性樹脂組成物。
- さらに、1分子内に2個以上のイソシアネート基、又はブロック化イソシアネート基有する化合物を含有することを特徴とする請求項1から請求項3のいずれか1項に記載の光硬化性樹脂組成物。
- さらに、ウレタン化触媒を含有することを特徴とする請求項1から請求項4のいずれか1項に記載の光硬化性樹脂組成物。
- さらに、熱硬化性成分を含有することを特徴とする請求項1から請求項5のいずれか1項に記載の光硬化性樹脂組成物。
- さらに、着色剤を含有することを特徴とする請求項1から請求項6のいずれか1項に記載の光硬化性樹脂組成物。
- 請求項1から請求項7のいずれか1項に記載の光硬化性樹脂組成物を、基材上に塗布し、光硬化させて得られる硬化物。
- 前記基材は、銅層であることを特徴とする請求項8に記載の硬化物。
- 塗布された前記光硬化性樹脂組成物は、パターン状に光硬化されることを特徴とする請求項8又は請求項9に記載の硬化物。
- 請求項1から請求項7のいずれか1項に記載の光硬化性樹脂組成物を、キャリアフィルムに塗布し、乾燥させて得られる光硬化性ドライフィルム。
- 請求項11に記載の光硬化性ドライフィルムを基材上に貼り付け、光硬化させて得られる硬化物。
- 前記基材は、銅層であることを特徴とする請求項12に記載の硬化物。
- 貼り付けられた前記光硬化性ドライフィルムは、パターン状に光硬化されることを特徴とする請求項12又は請求項13に記載の硬化物。
- 請求項8から請求項14のいずれか1項に記載の硬化物を備えるプリント配線板。
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