JP5409954B1 - 導電性樹脂組成物及びその硬化物 - Google Patents
導電性樹脂組成物及びその硬化物 Download PDFInfo
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- JP5409954B1 JP5409954B1 JP2013156773A JP2013156773A JP5409954B1 JP 5409954 B1 JP5409954 B1 JP 5409954B1 JP 2013156773 A JP2013156773 A JP 2013156773A JP 2013156773 A JP2013156773 A JP 2013156773A JP 5409954 B1 JP5409954 B1 JP 5409954B1
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- containing resin
- aromatic ring
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- conductive
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- 125000003118 aryl group Chemical group 0.000 claims abstract description 62
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- QCTJRYGLPAFRMS-UHFFFAOYSA-N prop-2-enoic acid;1,3,5-triazine-2,4,6-triamine Chemical class OC(=O)C=C.NC1=NC(N)=NC(N)=N1 QCTJRYGLPAFRMS-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- MHZDONKZSXBOGL-UHFFFAOYSA-N propyl dihydrogen phosphate Chemical compound CCCOP(O)(O)=O MHZDONKZSXBOGL-UHFFFAOYSA-N 0.000 description 1
- PRAHMDIEZMWIRW-UHFFFAOYSA-N propyl dihydrogen phosphite Chemical compound CCCOP(O)O PRAHMDIEZMWIRW-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 229940107700 pyruvic acid Drugs 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 239000011973 solid acid Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229960002317 succinimide Drugs 0.000 description 1
- XTQHKBHJIVJGKJ-UHFFFAOYSA-N sulfur monoxide Chemical group S=O XTQHKBHJIVJGKJ-UHFFFAOYSA-N 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- LRBQNJMCXXYXIU-NRMVVENXSA-N tannic acid Chemical compound OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-NRMVVENXSA-N 0.000 description 1
- 235000015523 tannic acid Nutrition 0.000 description 1
- 229940033123 tannic acid Drugs 0.000 description 1
- 229920002258 tannic acid Polymers 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 230000002123 temporal effect Effects 0.000 description 1
- WMXCDAVJEZZYLT-UHFFFAOYSA-N tert-butylthiol Chemical compound CC(C)(C)S WMXCDAVJEZZYLT-UHFFFAOYSA-N 0.000 description 1
- UGNWTBMOAKPKBL-UHFFFAOYSA-N tetrachloro-1,4-benzoquinone Chemical class ClC1=C(Cl)C(=O)C(Cl)=C(Cl)C1=O UGNWTBMOAKPKBL-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 229940035024 thioglycerol Drugs 0.000 description 1
- NJRXVEJTAYWCQJ-UHFFFAOYSA-N thiomalic acid Chemical compound OC(=O)CC(S)C(O)=O NJRXVEJTAYWCQJ-UHFFFAOYSA-N 0.000 description 1
- NBOMNTLFRHMDEZ-UHFFFAOYSA-N thiosalicylic acid Chemical compound OC(=O)C1=CC=CC=C1S NBOMNTLFRHMDEZ-UHFFFAOYSA-N 0.000 description 1
- 229940103494 thiosalicylic acid Drugs 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- CYTQBVOFDCPGCX-UHFFFAOYSA-N trimethyl phosphite Chemical compound COP(OC)OC CYTQBVOFDCPGCX-UHFFFAOYSA-N 0.000 description 1
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 125000002256 xylenyl group Chemical class C1(C(C=CC=C1)C)(C)* 0.000 description 1
- 125000006839 xylylene group Chemical group 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical class O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
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- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
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- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
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Abstract
【解決手段】本発明の導電性樹脂組成物は、芳香環を有さない水酸基及びカルボキシル基含有樹脂、導電性粉末、多官能アクリレートモノマー、光重合開始剤、及び、ブロックイソシアネートを含み、前記芳香環を有さない水酸基及びカルボキシル基含有樹脂の水酸基当量の合計が300以上3000以下である。
【選択図】なし
Description
このカルボキシル基含有樹脂は、芳香環を有さない構造とすることにより、カルボキシル基含有樹脂自体の光吸収を抑え、相対的に(メタ)アクリレートモノマーの光反応性を向上できる。
(2)不飽和二重結合を有する酸無水物と、それ以外の不飽和二重結合を有する化合物の共重合体に、水酸基を有する化合物を反応させて得られる水酸基及びカルボキシル基含有樹脂、
(3)エポキシ基と不飽和二重結合を有する化合物と不飽和二重結合を有する化合物の共重合体に、飽和カルボン酸を反応させ、生成した2級の水酸基に多塩基酸無水物を反応させて得られる水酸基及びカルボキシル基含有樹脂、
(4)水酸基含有ポリマーに多塩基酸無水物を反応させて得られる水酸基及びカルボキシル基含有樹脂が挙げられるが、これらに限定されるものではない。
なお、本明細書において、(メタ)アクリル酸とは、アクリル酸、メタクリル酸及びそれらの混合物を総称する用語で、他の類似の表現についても同様である。
また、上記カルボキシル基含有樹脂の酸価は、40〜200mgKOH/gの範囲であることが好ましく、より好ましくは45〜120mgKOH/gの範囲である。カルボキシル基含有樹脂の酸価が40mgKOH/g未満であるとアルカリ現像が困難となり、一方、200mgKOH/gを超えると現像液による露光部の溶解が進むために、必要以上にラインが痩せたり、場合によっては、露光部と未露光部の区別なく現像液で溶解剥離してしまい、正常な導電パターンの描画が困難となるので好ましくない。
(2)・・・無水マレイン酸などの不飽和二重結合を有する酸無水物と、それ以外の不飽和二重結合を有する化合物とを共重合することにより得られる芳香環を有さないカルボキシル基含有樹脂が挙げられるが、これらに限定されるものではない。
導電性粉末は、導電性粉末の材質は、導電性樹脂組成物において導電性を付与するものであればいかなるものでも用いることができる。このような導電性粉末としては、Ag、Au、Pt、Pd、Ni、Cu、Al、Sn、Pb、Zn、Fe、Ir、Os、Rh、W、Mo、Ru等を挙げることができ、これらの中でもAgが好ましい。これらの導電性粉末は、上記成分単体の形態で用いてもよいが、合金や、酸化物の形態で用いてもよい。さらに、酸化錫(SnO2)、酸化インジウム(In2O3)、ITO(Indium Tin Oxide)などを用いることもできる。なお、導電性粉末としては、カーボンブラック、グラファイト、カーボンナノチューブなどの炭素粉でもよいが、これらを用いると、光透過性が低下するため、注意を要する。
(メタ)アクリレートモノマーとして、多官能(メタ)アクリレートモノマー(2官能以上の(メタ)アクリレートモノマー)を用いる。多官能(メタ)アクリレートモノマーを用いる理由は、官能基の数が1つの場合よりも、光反応性が向上して解像性が優れるためである。
X1は、アクリロイルオキシ基を含む基を表す。
Z1はアルキレン基を表す。
光重合開始剤としては、特に限定されず、ベンゾイン系、フォスフィンオキサイド系でもよいが、下記一般式(V)で表される基を有するオキシムエステル系、又は、下記一般式(VI)で表される基を有するアセトフェノン系光重合開始剤を使用することが好ましい。
導電性樹脂組成物から得られる硬化膜の強靭性及び下地基材との密着性を向上させるために1分子内にブロック化イソシアネート基を有する化合物、すなわちブロックイソシアネート化合物を配合する。また、ブロックイソシアネート化合物を配合することにより耐熱性等も付与することができる。
51、7960、7961、7982、7990、7991、7992(以上、Baxenden社製、商品名)スミジュールBL−3175、BL−4165、BL−1100、BL−1265 、デスモジュールTPLS−2957 、TPLS−2062、TPLS−2078、TPLS−2117、デスモサーム2170、デスモサーム2265( 以上、住友バイエルウレタン社製、商品名)、コロネート2512、コロネート2513、コロネート2520( 以上、日本ポリウレタン工業社製、商品名)、B−830、B−815、B−846、B−870、B−874、B−882(三井武田ケミカル社製、商品名)、TPA−B80E、17B−60PX、E402−B80T、MF−B60B、MF−K60B、SBN−70D(旭化成ケミカルズ社製、商品名)、カレンズMOI−BM(昭和電工社製、商品名)等が挙げられる。なお、スミジュールBL−3175、BL−4265はブロック剤としてメチルエチルオキシムを用いて得られるものである。
有機酸としては、芳香環を持たない有機酸が好ましい。芳香環を持たない有機酸を配合することにより、有機酸自体の光吸収性が抑制され、相対的に4官能基の(メタ)アクリレートモノマーの光反応性が向上し、優れた解像性を得ることができる。
分散剤を配合することで、導電性樹脂組成物の分散性、沈降性を改善することができる。
光重合禁止剤を添加することで、露光による導電性樹脂組成物内部でおこるラジカル重合の内、重合禁止剤の種類およびその添加量に応じた一定量のラジカル重合を抑制できる。これにより散乱光のような弱い光に対しての光反応を抑制することができる。よって、より微細な導電パターン膜のラインをシャープに形成することができるため、好ましく用いることができる。光重合禁止剤は、光重合禁止剤として使用できるものであれば特に制限はなく、例えば、p−ベンゾキノン、ナフトキノン、ジ−t−ブチル・パラクレゾール、ヒドロキノンモノメチルエーテル、α−ナフトール、アセトアミジンアセテート、ヒドラジン塩酸塩、トリメチルベンジルアンモニウムクロリド、ジニトロベンゼン、ピクリン酸、キノンジオキシム、ピロガロール、タンニン酸、レゾルジン、クペロン、フェノチアジン、などが挙げられる。
本発明の導電性樹脂組成物には、その塗膜の物理的強度等を上げるために、必要に応じて、フィラーを配合することができる。このようなフィラーとしては、公知慣用の無機又は有機フィラーが使用できるが、特に硫酸バリウム、シリカ、ハイドロタルサイト及びタルクが好ましく用いられる。
本発明の導電性樹脂組成物に、上記分子中に2つ以上の環状(チオ)エーテル基を有する熱硬化性成分を使用する場合、熱硬化触媒を含有することが好ましい。そのような熱硬化触媒としては、例えば、イミダゾール、2−メチルイミダゾール、2−エチルイミダゾール、2−エチル−4−メチルイミダゾール、2−フェニルイミダゾール、4−フェニルイミダゾール、1−シアノエチル−2−フェニルイミダゾール、1−(2−シアノエチル)−2−エチル−4−メチルイミダゾール等のイミダゾール誘導体;ジシアンジアミド、ベンジルジメチルアミン、4−(ジメチルアミノ)−N,N−ジメチルベンジルアミン、4−メトキシ−N,N−ジメチルベンジルアミン、4−メチル−N,N−ジメチルベンジルアミン等のアミン化合物、アジピン酸ジヒドラジド、セバシン酸ジヒドラジド等のヒドラジン化合物;トリフェニルホスフィン等のリン化合物などが挙げられる。また、市販されているものとしては、例えば四国化成工業社製の2MZ−A、2MZ−OK、2PHZ、2P4BHZ、2P4MHZ(いずれもイミダゾール系化合物の商品名)、サンアプロ社製のU−CAT(登録商標)3503N、U−CAT3502T(いずれもジメチルアミンのブロックイソシアネート化合物の商品名)、DBU、DBN、U−CATSA102、U−CAT5002(いずれも二環式アミジン化合物及びその塩)などが挙げられる。特に、これらに限られるものではなく、エポキシ樹脂やオキセタン化合物の熱硬化触媒、もしくはエポキシ基及びオキセタニル基の少なくとも何れか1種とカルボキシル基の反応を促進するものであればよく、単独で又は2種以上を混合して使用してもかまわない。また、グアナミン、アセトグアナミン、ベンゾグアナミン、メラミン、2,4−ジアミノ−6−メタクリロイルオキシエチル−S−トリアジン、2−ビニル−2,4−ジアミノ−S−トリアジン、2−ビニル−4,6−ジアミノ−S−トリアジン・イソシアヌル酸付加物、2,4−ジアミノ−6−メタクリロイルオキシエチル−S−トリアジン・イソシアヌル酸付加物等のS−トリアジン誘導体を用いることもでき、好ましくはこれら密着性付与剤としても機能する化合物を前記熱硬化触媒と併用する。
熱重合禁止剤は、本発明の導電性樹脂組成物の熱的な重合または経時的な重合を防止するために用いることができる。熱重合禁止剤としては例えば、4−メトキシフェノール、ハイドロキノン、アルキルまたはアリール置換ハイドロキノン、t−ブチルカテコール、ピロガロール、2−ヒドロキシベンゾフェノン、4−メトキシ−2−ヒドロキシベンゾフェノン、塩化第一銅、フェノチアジン、クロラニル、ナフチルアミン、β−ナフトール、2,6−ジ−t−ブチル−4−クレゾール、2,2’−メチレンビス(4−メチル−6−t−ブチルフェノール)、ピリジン、ニトロベンゼン、ジニトロベンゼン、ピクリン酸、4−トルイジン、メチレンブルー、銅と有機キレート剤反応物、サリチル酸メチル、及びフェノチアジン、ニトロソ化合物、ニトロソ化合物とAlとのキレートなどが挙げられる。
本発明の導電性樹脂組成物において、感度を向上するために、連鎖移動剤として公知のNフェニルグリシン類、フェノキシ酢酸類、チオフェノキシ酢酸類、メルカプトチアゾール等を用いることができる。連鎖移動剤の具体例を挙げると、例えば、メルカプト琥珀酸、メルカプト酢酸、メルカプトプロピオン酸、メチオニン、システイン、チオサリチル酸及びその誘導体等のカルボキシル基を有する連鎖移動剤;メルカプトエタノール、メルカプトプロパノール、メルカプトブタノール、メルカプトプロパンジオール、メルカプトブタンジオール、ヒドロキシベンゼンチオール及びその誘導体等の水酸基を有する連鎖移動剤;1−ブタンチオール、ブチル−3−メルカプトプロピオネート、メチル−3−メルカプトプロピオネート、2,2−(エチレンジオキシ)ジエタンチオール、エタンチオール、4−メチルベンゼンチオール、ドデシルメルカプタン、プロパンチオール、ブタンチオール、ペンタンチオール、1−オクタンチオール、シクロペンタンチオール、シクロヘキサンチオール、チオグリセロール、4,4−チオビスベンゼンチオール等である。
本発明の導電性樹脂組成物には、公知慣用の成分、例えば増粘剤、消泡・レベリング剤、カップリング剤、酸化防止剤、防錆剤等を、必要に応じて適宜配合することができることは勿論である。
次に、本発明に係る導電性樹脂組成物を用いて硬化物を形成する方法の一例について説明する。
本発明の導電性樹脂組成物に関し、上述した各必須成分、ならびに任意成分との混練分散は、三本ロールやブレンダー等の機械が用いられる。
こうして分散された導電性樹脂組成物は、スクリーン印刷法、バーコーター、ブレードコーターなど適宜の塗布方法で基材上に塗布される。次いで指触乾燥性を得るために熱風循環式乾燥炉、遠赤外線乾燥炉等で、カルボキシル基含有樹脂が熱分解しない温度、例えば約60〜120℃で5〜40分程度乾燥させて有機溶剤を蒸発させ、タックフリーの塗膜を得る。
これらの工程では、500℃という高温で焼成しないので、基材として、耐熱性のない樹脂製の基材を使用することができる。具体的には、樹脂製の基材としては、例えば、ポリイミド、ポリエチレンテレフタレート(PET)、ポリブチレンテレフタレート(PBT)、ポリエチレンナフタレート(PEN)のようなポリエステル系樹脂、ポリエーテルサルフォン(PES)、ポリスチレン(PS)、ポリメチルメタクリレート(PMMA)、ポリカーボネート(PC)、ポリアミド(PA)、ポリプロピレン(PP)、ポリフェニレンオキサイド(PPO)等を挙げることができ、好適には、ポリエステル系樹脂を用いることができる。なお、ガラス基板等でもよい。
(配合成分)
合成例1[芳香環を有さない水酸基及びカルボキシル基含有樹脂]
温度計、攪拌機、滴下ロート、及び還流冷却器を備えたフラスコに、メチルメタクリレートとメタアクリル酸と2−ヒドロキシエチルアクリレートを47:15:38のモル比で仕込み、溶媒としてジプロピレングリコールモノメチルエーテル、触媒としてアゾビスイソブチロニトリルを入れ、窒素雰囲気下、80℃で6時間攪拌し、「芳香環を有さない水酸基及びカルボキシル基含有樹脂」ワニスを得た。このカルボキシル基含有樹脂は、水酸基当量が300であった。
温度計、攪拌機、滴下ロート、及び還流冷却器を備えたフラスコに、メチルメタクリレートとt-ブチルメタクリレートと2−ヒドロキシエチルアクリレートを62:15:23のモル比で仕込み、溶媒としてジプロピレングリコールモノメチルエーテル、触媒としてアゾビスイソブチロニトリルを入れ、窒素雰囲気下、80℃で6時間攪拌し、「芳香環を有さない水酸基含有樹脂」ワニスを得た。この水酸基含有樹脂は、水酸基当量が500であった。
温度計、攪拌機、滴下ロート、及び還流冷却器を備えたフラスコに、メチルメタクリレートとメタアクリル酸とt-ブチルメタクリレートを74:15:11のモル比で仕込み、溶媒としてジプロピレングリコールモノメチルエーテル、触媒としてアゾビスイソブチロニトリルを入れ、窒素雰囲気下、80℃で6時間攪拌し、「芳香環を有さないカルボキシル基含有樹脂」ワニスを得た。このカルボキシル基含有樹脂は、水酸基を含まない。
球状の導電性粉末:Ag粉末(最大粒径30μm以下、平均粒径2μm(SEM)))
[アクリレートモノマー]
4官能(メタ)アクリレートモノマー:商品名;NKオリゴU-4HA(新中村化学社製)
[光重合開始剤]
商品名 :IRGACURE 379EG(BASFジャパン社製),2-(ジメチルアミノ)-2-[(4-メチル
フェニル)メチル]-1-[4-(4-モルホリニル)フェニル]-1-ブタノン
[ブロックイソシアネート]
商品名 BI7982(Baxenden社製)イソシアネートHDI3量体 ブロック剤 Dimethylpyrazole
[有機酸]
2,2‘−チオ二酢酸
[分散剤]
商品名 DISPERBYK-111(ビックケミー・ジャパン社製)
(評価方法)
試験片作成:
ポリエステル樹脂製の基材上に、評価用の各導電性樹脂組成物を300メッシュのポリエステルスクリーンを用いて全面に塗布し、次いで、熱風循環式乾燥炉に80℃で30分間乾燥して指触乾燥性の良好な塗膜を形成した。その後、光源として高圧水銀灯を用い、ネガマスクを介して、導電性樹脂組成物上の積算光量が200mJ/cm2となるようにパターン露光した後、液温30℃の0.4質量%Na2CO3水溶液を用いて現像を行い、水洗した。最後に、140℃×30分で乾燥し、導電パターン膜を形成した試験片を作成した。
実施例1、2、3、4、6の場合:各バインダーの水酸基当量×配合割合(%)の合計
実施例5、7の場合:各バインダーの水酸基当量×100/配合量の合計
*2 水酸基を含まないことの意
比較例1、2、3、4、5、7の場合:各バインダーの水酸基当量×配合割合(%)の合計
比較例3、6の場合:各バインダーの水酸基当量×100/配合量の合計
*2 水酸基を含まないことの意
実施例1〜7から、本発明に係る導電性樹脂組成物では、熱に弱い基材に適用可能で、優れた導電性及び解像性を確保できるとともに、更に過酷な条件下においても、塗膜強度、下地基材との密着性のいずれも優れた導電性樹脂組成物を得ることができることが確認された。
Claims (6)
- 芳香環を有さない水酸基及びカルボキシル基含有樹脂、導電性粉末、多官能アクリレートモノマー、光重合開始剤、及び、ブロックイソシアネートを含み、前記芳香環を有さない水酸基及びカルボキシル基含有樹脂の水酸基当量の合計が300以上3000以下であることを特徴とする導電性樹脂組成物。
- 芳香環を有さない水酸基及びカルボキシル基含有樹脂、芳香環を有さない水酸基含有樹脂、及び芳香環を有さないカルボキシル基含有樹脂の群から選択された二種以上の樹脂、導電性粉末、多官能アクリレートモノマー、光重合開始剤、及び、ブロックイソシアネートを含み、前記二種以上の樹脂の水酸基当量の合計が300以上3000以下であることを特徴とする導電性樹脂組成物。
- 前記芳香環を有さない水酸基及びカルボキシル基含有樹脂は二重結合を含まないことを特徴とする請求項1記載の導電性樹脂組成物。
- 前記芳香環を有さない水酸基及びカルボキシル基含有樹脂、芳香環を有さない水酸基含有樹脂、及び芳香環を有さないカルボキシル基含有樹脂の群から選択された二種以上の樹脂は、いずれも二重結合を含まないことを特徴とする請求項2記載の導電性樹脂組成物。
- 前記導電性樹脂組成物は導電回路形成用であることを特徴とする請求項1〜4のいずれかに記載の導電性樹脂組成物。
- 基材上に、請求項1〜5のいずれかに記載の樹脂組成物を、塗布、乾燥して形成されてなる硬化物。
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