JP5420311B2 - 溶剤組成物 - Google Patents
溶剤組成物 Download PDFInfo
- Publication number
- JP5420311B2 JP5420311B2 JP2009118415A JP2009118415A JP5420311B2 JP 5420311 B2 JP5420311 B2 JP 5420311B2 JP 2009118415 A JP2009118415 A JP 2009118415A JP 2009118415 A JP2009118415 A JP 2009118415A JP 5420311 B2 JP5420311 B2 JP 5420311B2
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- Prior art keywords
- compound
- solvent composition
- dyes
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- carbon
- Prior art date
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- 238000009835 boiling Methods 0.000 claims description 11
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Description
また、溶解性の観点からは、β−メトキシプロピオン酸メチルやβ−エトキシプロピオン酸エチル等のβ−アルコキシプロピオン酸アルキルエステル類が最も好ましいと考えられているが、これらも高分子化合物或いは各種添加剤の溶解性が未だ満足できるものではなく、更に塗布後の揮発性の点でも未だ満足できるものではない。
本発明の溶剤組成物は、(a)上記一般式(I)で表される炭素縮合環二環化合物、及び(b)上記一般式(II)で表されるジフェニルメタン化合物を含有してなるものである。
また、本発明の溶剤組成物においては、(a)成分である炭素縮合環二環化合物及び(b)成分であるジフェニルメタン化合物の合計含有量が、本発明の溶剤組成物中、50〜100質量%であることが好ましく、75〜100質量%であることが更に好ましく、(a)炭素縮合環二環化合物の含有量が、(a)炭素縮合環二環化合物及び(b)ジフェニルメタン化合物の合計含有量に対して20質量%以上であるのが好ましく、30質量%以上70質量%以下であるのが更に好ましい。
他の有機溶剤としては、メタノール、エタノール、プロパノール、イソプロパノール、ブタノール、3−メチルブタノール、メチルイソブチルカルビノール、ヘプタノール、オクタノール、2−エチル−1−ヘキサノール、3,3,5−トリメチル−1−ヘキサノール、ノナノール、シクロヘキサノール、ベンジルアルコール、ナフチルアルコール、フッ素化アルコール等のアルコール類;エチレングリコール、ジエチレングリコール、トリエチレングリコール、ポリエチレングリコール、プロピレングリコール、ジプロピレングリコール、ポリプロピレングリコール等のグリコール類;3−メトキシブタノール、3−メチル−3−メトキシブタノール、エチレングリコールモノメチルエーテル(メチルセルソルブ)、エチレングリコールモノエチルエーテル(セルソルブ)、エチレングリコールモノブチルエーテル(ブチルセルソルブ)、ジエチレングリコールモノエチルエーテル(カルビトール)、ジエチレングリコールモノブチルエーテル(ブチルカルビトール)、プロピレングリコールモノメチルエーテル等のエーテルアルコール類;アセトン、メチルエチルケトン、メチルイソブチルケトン、シクロヘキサノン、イソホロン等のケトン類;ピロリドン、N−メチルピロリドン、テトラヒドロフラン、オキサゾール、ベンゾフラン、ジオキサン等のヘテロ複素環式化合物;ジメチルホルムアミド、ジメチルアセトアミド等のアミド類ジメチルスルホキシド、スルホラン等のスルホン類;酢酸メチル、酢酸エチル、酢酸ブチル、酢酸アミル、3−メトキシブチルアセテート、3−メチル−3−メトキシブチルアセテート、2−エチルヘキシルアセテート、シクロヘキシルアセテート、ベンジルアセテート、乳酸メチル、乳酸エチル、乳酸ブチル、3−メトキシプロピオン酸メチル、3−エトキシプロピオン酸エチル等のエステル類;ジベンジルエーテル、アニソール等のエーテル類;ニトロエタン、ニトロメタン等のニトロ化合物;アセトニトリル等のニトリル化合物;γ−ブチロラクトン等のラクトン類;エチレングリコールモノメチルエーテルアセテート、エチレングリコールモノエチルエーテルアセテート、プロピレングリコールモノメチルエーテルアセテート等 のエーテルエステル類;ベンゼン、トルエン、キシレン、クメン、シメン、ジヘキシルベンゼン、テトラメチルベンゼン、ジエチルベンゼン、ジブチルベンゼン、シクロヘキシルベンゼン、ビフェニル、メシチレン、ベンジルトルエン等の芳香族炭化水素;デカリン、アルキルデカリン、テトラリン等の縮合環炭化水素;n−ヘキサン、n−ヘプタン、ミネラルスピリット等の脂肪族炭化水素;シクロヘキサン、アルキルシクロヘキサン、アルキルシクロペンタン等の脂環式炭化水素等が挙げられる。
本発明における水及び/又は他の有機溶剤の使用量は、0〜10質量%、特に0〜5質量%であることが好ましい。
〔表1〕に示した配合にて溶剤組成物S1〜S14をそれぞれ作製した。ただし、化合物の含有量は質量%を示す。
〔表2〕に示した配合にて溶剤組成物HS14〜HS29をそれぞれ作製した。ただし、化合物の含有量は質量%を示す。
上記の実施例及び比較例により得られた溶剤組成物について、以下の評価及び測定を実施した。
被験者10名による官能試験で、○:ほとんど臭気なし、△:臭気あり、×:強い臭気あり、の3段階にて評価した。
上記溶剤組成物98質量部に、〔表3〕及び〔表4〕に示した溶質(表3の注釈に記載の有機化合物)を2質量部加えて室温で1時間撹拌した後、溶解性を観察し、○:完全に溶解した、△:50℃で1時間撹拌した後完全に溶解した、×:不溶物が認められた、の3段階にて評価した。尚、○→×は、溶液を室温で3日間放置した時に溶解性の評価が○から×に経時変化したことを表す。
上記溶解性評価において調製した溶液のうち溶質として6,13−ビス(トリイソプロピルシリルエチニル)ペンタセンを含有するものを、厚さ0.7mmの透明ガラス基板上にスクリーン印刷機(ミノグループ製;WHT刷台3号)で印刷後、減圧下135℃で乾燥を行った。室温まで冷却後、膜面が均質であれば○、一部ムラがあれば△、全面的にムラ或いは結晶があれば×の3段階にて評価した。
上記溶剤組成物について、E型粘度計で20℃における粘度及び1気圧における沸点を測定した。
中性洗剤で洗浄した後、超純水ですすいで乾燥したガラス(松浪硝子工業(株)製;MICRO SLIDE GLASS S 1226)上に、上記溶剤組成物を10μL滴下し、協和界面科学(株)製CONTACT−ANGLE METER CA−Dを用いて接触角を測定した。測定時の気温は22〜25℃、湿度は50〜70%であった。接触角は、6回測定し、最大値及び最小値を除いた値の平均値とした(単位;°)。
尚、接触角が20°を超える場合には塗付が困難となり、15°以下である場合にはとりわけ塗布が良好となる。
これに対し、特定の炭素縮合環二環化合物及び特定のジフェニルメタン化合物を含有してなる本発明の溶剤組成物は、接触角が小さく、粘度が低く沸点が高いため溶剤が揮発しにくく、膜面が均質になるので塗膜性及び製膜性に優れたものである(実施例1、9〜12及び14)。
Claims (5)
- (a)下記一般式(I)で表される炭素縮合環二環化合物、及び(b)下記一般式(II)で表されるジフェニルメタン化合物を含有してなることを特徴とする溶剤組成物。
- (a)炭素縮合環二環化合物の含有量が、(a)炭素縮合環二環化合物及び(b)ジフェニルメタン化合物の合計含有量に対して20質量%以上であることを特徴とする請求項1記載の溶剤組成物。
- (a)炭素縮合環二環化合物の含有量が、(a)炭素縮合環二環化合物及び(b)ジフェニルメタン化合物の合計含有量に対して30質量%以上70質量%以下であることを特徴とする請求項1又は2記載の溶剤組成物。
- 20℃における粘度が4mPa・s以下であることを特徴とする請求項1〜3の何れか1項に記載の溶剤組成物。
- 1気圧における沸点が250℃以上であることを特徴とする請求項1〜4の何れか1項に記載の溶剤組成物。
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