JP2011195717A - 活性エネルギー線硬化型蛍光インキ組成物および該組成物を用いてなる印刷物 - Google Patents
活性エネルギー線硬化型蛍光インキ組成物および該組成物を用いてなる印刷物 Download PDFInfo
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- JP2011195717A JP2011195717A JP2010064369A JP2010064369A JP2011195717A JP 2011195717 A JP2011195717 A JP 2011195717A JP 2010064369 A JP2010064369 A JP 2010064369A JP 2010064369 A JP2010064369 A JP 2010064369A JP 2011195717 A JP2011195717 A JP 2011195717A
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- Prior art keywords
- acrylate
- meth
- active energy
- energy ray
- resin
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- 239000000203 mixture Substances 0.000 title claims abstract description 32
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims abstract description 72
- 229920005989 resin Polymers 0.000 claims abstract description 66
- 239000011347 resin Substances 0.000 claims abstract description 66
- 239000003208 petroleum Substances 0.000 claims abstract description 48
- 239000000178 monomer Substances 0.000 claims abstract description 27
- 229920000877 Melamine resin Polymers 0.000 claims abstract description 17
- 239000007850 fluorescent dye Substances 0.000 claims abstract description 16
- 239000004640 Melamine resin Substances 0.000 claims abstract description 15
- 238000007639 printing Methods 0.000 claims description 11
- 229920001577 copolymer Polymers 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 239000000758 substrate Substances 0.000 claims description 2
- 238000003860 storage Methods 0.000 abstract description 10
- 239000003505 polymerization initiator Substances 0.000 abstract 2
- 239000000976 ink Substances 0.000 description 40
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 13
- 229920003270 Cymel® Polymers 0.000 description 12
- 239000003999 initiator Substances 0.000 description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 9
- -1 DIRECT YELLOW 85 Chemical compound 0.000 description 8
- 238000006266 etherification reaction Methods 0.000 description 7
- 239000000049 pigment Substances 0.000 description 7
- 239000001993 wax Substances 0.000 description 7
- 125000000217 alkyl group Chemical group 0.000 description 6
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- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 6
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- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 4
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- 230000000052 comparative effect Effects 0.000 description 4
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- 125000004432 carbon atom Chemical group C* 0.000 description 3
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- VYXSBFYARXAAKO-UHFFFAOYSA-N ethyl 2-[3-(ethylamino)-6-ethylimino-2,7-dimethylxanthen-9-yl]benzoate;hydron;chloride Chemical compound [Cl-].C1=2C=C(C)C(NCC)=CC=2OC2=CC(=[NH+]CC)C(C)=CC2=C1C1=CC=CC=C1C(=O)OCC VYXSBFYARXAAKO-UHFFFAOYSA-N 0.000 description 3
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- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 2
- BKOOMYPCSUNDGP-UHFFFAOYSA-N 2-methylbut-2-ene Chemical compound CC=C(C)C BKOOMYPCSUNDGP-UHFFFAOYSA-N 0.000 description 2
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
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- 239000004641 Diallyl-phthalate Substances 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
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- XUMBMVFBXHLACL-UHFFFAOYSA-N Melanin Chemical compound O=C1C(=O)C(C2=CNC3=C(C(C(=O)C4=C32)=O)C)=C2C4=CNC2=C1C XUMBMVFBXHLACL-UHFFFAOYSA-N 0.000 description 2
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- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 229920000180 alkyd Polymers 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 2
- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 description 2
- 239000001913 cellulose Chemical class 0.000 description 2
- 229920002678 cellulose Chemical class 0.000 description 2
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 2
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- 238000005227 gel permeation chromatography Methods 0.000 description 2
- 238000001879 gelation Methods 0.000 description 2
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- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
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Abstract
【解決手段】0.5〜10重量%の蛍光染料、25〜35重量%のメラミン樹脂、3〜10重量%の石油樹脂、5〜20重量%の光重合性アクリレートモノマーおよび5〜15重量%の光重合開始剤を含有する活性エネルギー線硬化型蛍光インキ組成物。
【選択図】なし
Description
しかしながら、何れも油性インキとなっており、蛍光染料を含有する活性エネルギー線硬化型蛍光インキを実現するためには、貯蔵安定性の面より実現が困難な状況であった。
一般式(1)
一般式(2)
一般式(3)
・蛍光染料 0.5〜10重量%
・メラミン樹脂 25〜35重量%
・石油樹脂 3〜10重量%
・光重合成アクリレートモノマー 5〜20重量%
・光重合開始剤 5〜15重量%
・非反応性樹脂 0〜35重量%
・添加剤 0〜10重量%
さらに、好ましくは、以下が例示される。
・蛍光染料 1〜 5重量%
・メラミン樹脂 25〜35重量%
・石油樹脂 3〜10重量%
・光重合成アクリレートモノマー 5〜20重量%
・光重合開始剤 5〜15重量%
・非反応性樹脂 25〜35重量%
・添加剤 1〜10重量%
一般式(1)
一般式(2)
一般式(3)
重量平均分子量100〜6000のエチレン性不飽和二重結合を有するモノマーとは、
・単官能または多官能の(メタ)アクリレート類
および
・エチレン性不飽和二重結合を有するオリゴマー(反応性オリゴマー)
をいい、これらを適宜用いることでインキ組成物の粘度を調整することが出来る。
重量平均分子量100〜6000のエチレン性不飽和二重結合を有するモノマーはインキ組成物を基準として 5〜20重量%の範囲で用いられることが好ましい。
[実施例1〜9]
非反応性樹脂が、処方に含まれる場合(実施例1〜4、比較例1〜3)は、予め石油樹脂および非反応性樹脂と光重合性アクリレートモノマーとを昇温加熱混合(上限温度を100℃の留め)させ、光重合性アクリレートモノマーに溶解させておく。
インキ組成物は、表1に示す所定の配合割合にて、バタフライミキサーを用いて攪拌混合し、3本ロールにて最大粒径が7.5μm以下になるように分散してインキ組成物を作成し、且つスプレッドメーターにて一定の粘度規格と成るよう調整して、各インキ組成物を作製した。
貯蔵安定性試験として、実施例1〜4、比較例1〜3で作成したインキ 1.0kgを亜鉛銅版製容器に貯蔵し(上部空間は空気)25℃と60℃の条件下に放置する。そのインキの状態を以下の基準にて評価し、結果を表3、4に示す。
○:変化なし
△:インキ缶底部より20%が固化している
×:インキ缶底部より80%が固化している
(△・×では、インキが固化しゲル化していると判断)
なお60℃で20日間の条件は、常温放置では6か月間に相当するものであり、実用的にはこの程度の保存安定性が必須である。
実際、実施例1〜4を常温にて放置した結果、6か月以上ゲル化を引き起こさなかった。
さらに、実施例1〜4を実機(小森コーポレーション社製 枚葉印刷機リスロン26)にて、1万枚印刷を行った結果、適正に印刷が行われた。
Claims (4)
- 0.5〜10重量%の蛍光染料、25〜35重量%のメラミン樹脂、3〜10重量%の石油樹脂、5〜20重量%の光重合性アクリレートモノマーおよび5〜15重量%の光重合開始剤を含有することを特徴とする活性エネルギー線硬化型蛍光インキ組成物。
- 光重合性アクリレートモノマーが、重量平均分子量100〜6000のエチレン性不飽和二重結合を有するモノマーであることを特徴とする請求項1または2記載の活性エネルギー線硬化型蛍光インキ組成物。
- 請求項1〜3いずれか記載の活性エネルギー線硬化型蛍光インキ組成物を基材上に印刷してなる活性エネルギー線硬化型蛍光インキ印刷物。
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS617366A (ja) * | 1984-06-22 | 1986-01-14 | Ricoh Co Ltd | 熱転写記録媒体 |
JP2000517363A (ja) * | 1996-08-30 | 2000-12-26 | デイ―グロ カラー コーポレイション | 放射線硬化性蛍光印刷インク |
JP2004359767A (ja) * | 2003-06-03 | 2004-12-24 | Toyo Ink Mfg Co Ltd | 活性エネルギー線硬化性乾式平版印刷インキ組成物、印刷方法およびその印刷物 |
JP2009506187A (ja) * | 2005-08-31 | 2009-02-12 | プリンター リミテッド | Uv硬化可能なハイブリッド硬化インクジェットインク組成物およびそれを使用するソルダマスク |
-
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- 2010-03-19 JP JP2010064369A patent/JP5533098B2/ja active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS617366A (ja) * | 1984-06-22 | 1986-01-14 | Ricoh Co Ltd | 熱転写記録媒体 |
JP2000517363A (ja) * | 1996-08-30 | 2000-12-26 | デイ―グロ カラー コーポレイション | 放射線硬化性蛍光印刷インク |
JP2004359767A (ja) * | 2003-06-03 | 2004-12-24 | Toyo Ink Mfg Co Ltd | 活性エネルギー線硬化性乾式平版印刷インキ組成物、印刷方法およびその印刷物 |
JP2009506187A (ja) * | 2005-08-31 | 2009-02-12 | プリンター リミテッド | Uv硬化可能なハイブリッド硬化インクジェットインク組成物およびそれを使用するソルダマスク |
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