JP3366716B2 - UV curable ink for printing stepped ball sheets - Google Patents

UV curable ink for printing stepped ball sheets

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Publication number
JP3366716B2
JP3366716B2 JP01487794A JP1487794A JP3366716B2 JP 3366716 B2 JP3366716 B2 JP 3366716B2 JP 01487794 A JP01487794 A JP 01487794A JP 1487794 A JP1487794 A JP 1487794A JP 3366716 B2 JP3366716 B2 JP 3366716B2
Authority
JP
Japan
Prior art keywords
water
soluble
ink
parts
curable ink
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
JP01487794A
Other languages
Japanese (ja)
Other versions
JPH07207208A (en
Inventor
健 田村
舜也 千眼
昭規 福井
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Osaka Printing Ink Manufacturing Co Ltd
Original Assignee
Osaka Printing Ink Manufacturing Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Osaka Printing Ink Manufacturing Co Ltd filed Critical Osaka Printing Ink Manufacturing Co Ltd
Priority to JP01487794A priority Critical patent/JP3366716B2/en
Publication of JPH07207208A publication Critical patent/JPH07207208A/en
Application granted granted Critical
Publication of JP3366716B2 publication Critical patent/JP3366716B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は段ボ−ルシ−ト等に対す
る印刷で,インキの無駄を無くし,印刷の直後に次の工
程が連続して行われ,生産性の向上とコストの低減を可
能ならしめる印刷方式に用いられる水可溶性紫外線硬化
型インキに関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention eliminates waste of ink in printing on a corrugated ball sheet and the like, and the next step is continuously performed immediately after printing to improve productivity and reduce cost. The present invention relates to a water-soluble UV-curable ink used in a printing method that enables printing.

【0002】[0002]

【従来の技術及びその問題点】従来,段ボ−ルシ−トの
印刷に用いられる印刷装置は,表面に微細な凹凸を形成
した主ロ−ル(アニロックスロ−ル)と補助ロ−ルを対
向配置し,主ロ−ルに版胴を接触させており,主ロ−ル
と補助ロ−ルとの間に,上方からパイプによってインキ
が流し込まれ,インキは,主ロ−ルと補助ロ−ルとの間
に溜まる。このインキ溜によって,インキが主ロ−ルの
凹部に入り,補助ロ−ルにより余分なインキが絞り取ら
れ,主ロ−ル上に均一なインキ皮膜が形成されて,版上
へと送られる。
2. Description of the Related Art A conventional printing apparatus used for printing a corrugated ball sheet has a main roll (anilox roll) having fine irregularities formed on its surface and an auxiliary roll. The printing cylinder is in contact with the main roll, and the ink is poured by a pipe from above between the main roll and the auxiliary roll. -It collects with Le. This ink reservoir causes the ink to enter the concave portion of the main roll, and the auxiliary roll squeezes out excess ink, forms a uniform ink film on the main roll, and sends it to the plate. .

【0003】この補助ロ−ルにより,インキが絞り取ら
れる時に強いずり応力がかかり,多量の熱を発生する。
従来,この装置に使用されるインキは,その組成中,溶
剤として低沸点の水及び水可溶性溶剤(アルコ−ルやグ
リコ−ル等)を使用した水性インキか,特開平5−13
8863号公報に記載されているようなインキ中に,水
を1〜25重量%含む水溶性紫外線硬化型インキであ
る。
With this auxiliary roll, a strong shear stress is applied when the ink is squeezed out, and a large amount of heat is generated.
Conventionally, the ink used in this apparatus is a water-based ink using low boiling water and a water-soluble solvent (alcohol, glycol, etc.) as a solvent in its composition, or JP-A-5-13.
It is a water-soluble UV-curable ink containing 1 to 25% by weight of water in the ink as described in JP-A-8863.

【0004】上記の装置及びインキを用いた段ボ−ルシ
−トへの印刷方法では,インキが水及び水可溶性溶剤を
使用しているため,段ボ−ルシ−ト上での乾燥は速い
が,印刷機上での低沸点成分の蒸発があり,粘度上昇を
起こすため過剰のインキを絶えず循環流動させなければ
ならない。そのため,常時インキを循環させる装置が必
要である。又インキの色替えの際,多量のインキが無駄
になり,その処理対策は重大な問題となっている。
In the method of printing on the stepped ball sheet using the above apparatus and ink, since the ink uses water and a water-soluble solvent, drying on the stepped ball sheet is fast. However, there is evaporation of low boiling point components on the printing machine, and the viscosity rises, so excess ink must be constantly circulated. Therefore, a device that constantly circulates the ink is required. In addition, when changing the color of ink, a large amount of ink is wasted, and measures to deal with it are a serious problem.

【0005】[0005]

【発明が解決しようとする課題】本発明は,従来インキ
の前述した様な欠点を解消し,印刷装置を簡素化し,且
つ印刷操作,切替え作業等を効率化することが可能な段
ボ−ルシ−ト印刷用水溶性紫外線硬化型インキを提供す
ることを目的とするものである。
DISCLOSURE OF THE INVENTION The present invention solves the above-mentioned drawbacks of conventional inks, simplifies the printing apparatus, and makes the printing operation, switching work, etc. efficient. -It is intended to provide a water-soluble ultraviolet-curable ink for printing.

【0006】[0006]

【課題を解決するための手段】このような本発明の目的
は,水可溶性成分が50〜100%にあり,且つ粘度が
1000cps(25℃)以下の範囲にある紫外線硬化
型組成物であって,水及び水可溶性溶剤を含まないこと
を特徴とする水可溶性紫外線硬化型インキにより達成さ
れる。
The object of the present invention is to provide an ultraviolet-curable composition having a water-soluble component content of 50 to 100% and a viscosity of 1000 cps (25 ° C.) or less. , A water-soluble UV-curable ink characterized by not containing water and a water-soluble solvent.

【0007】本発明で使用する水可溶性紫外線硬化型イ
ンキとは,水可溶性成分が50〜100%の範囲にあ
り,且つその粘度が1000cps(25℃)以下で,
水及び水可溶性溶剤を全く含まない事を特徴としてい
る。その組成は,(1)紫外線を照射することにより硬
化する光重合性ビニ−ルオリゴマ−(2)同じく光重合
性ビニ−ルモノマ−(3)光重合開始剤(4)重合禁止
剤(5)顔料の混合物よりなる。又,上記以外に必要と
あらば,光鋭感剤,耐摩擦強化剤,ゲル化剤,消泡剤,
分散剤を助剤として混入しても良い。
The water-soluble UV-curable ink used in the present invention has a water-soluble component in the range of 50 to 100% and a viscosity of 1000 cps (25 ° C.) or less,
It is characterized by not containing water and water-soluble solvent at all. Its composition is (1) a photopolymerizable vinyl oligomer that is cured by irradiation with ultraviolet rays (2) a photopolymerizable vinyl monomer (3) a photopolymerization initiator (4) a polymerization inhibitor (5) a pigment A mixture of. In addition to the above, if necessary, a photosensitizer, an anti-friction agent, a gelling agent, an antifoaming agent,
A dispersant may be mixed as an auxiliary agent.

【0008】(1)の光重合性オリゴマ−とは,エポキ
シアクリレ−ト,エポキシ化油アクリレ−ト,ウレタン
アクリレ−ト,ポリエステルアクリレ−ト,ポリエ−テ
ルアクリレ−ト,アクリルアルキッド,ジアリルフタレ
−ト樹脂など周知のオリゴアクリレ−トが挙げられ,ヒ
ドロキシル基,カルボキシル基,ポリプロピレン基,ア
ミノ基など親水性基を含有し,粘度が1500cps
(25℃)以下のものが好ましく,1000cps(2
5℃)以下のものがより好ましい。
The photopolymerizable oligomer (1) is an epoxy acrylate, an epoxidized oil acrylate, a urethane acrylate, a polyester acrylate, a polyether acrylate, an acrylic alkyd, a diallyl phthalate. Well-known oligoacrylates such as epoxy resin are included, which contain hydrophilic groups such as hydroxyl group, carboxyl group, polypropylene group and amino group, and have a viscosity of 1500 cps.
(25 ° C) or less is preferable, and 1000 cps (2
It is more preferably 5 ° C. or less.

【0009】(2)の光重合性ビニ−ルモノマ−とは,
例えば2−ヒドロキシエチルアクリレ−ト,2−メトキ
シエチルアクリレ−ト,2−ヒドロキシプロピルアクリ
レ−ト,4−ヒドロキシブチルアクリレ−ト,ポリエチ
レングリコ−ル #300ジアクリレ−ト,ポリエチレン
グリコ−ル #400ジアクリレ−ト,ポリエチレングリ
コ−ル #600ジアクリレ−ト,アルキルフェノキシポ
リエチレングリコ−ルアクリレ−ト,N,N −ジメチルア
ミノエチルアクリレ−ト,N,N −ジメチルアミノエチル
メタクリレ−ト,N −ビニ−ルピロリドン,モルホリン
アクリレ−ト,モルホリノエチルアクリレ−トなど水可
溶性ビニ−ルモノマ−が挙げられ,粘度が150cps
(25℃)以下のものが好ましく,100cps(25
℃)以下のものがより好ましい。
The photopolymerizable vinyl monomer (2) is
For example, 2-hydroxyethyl acrylate, 2-methoxyethyl acrylate, 2-hydroxypropyl acrylate, 4-hydroxybutyl acrylate, polyethylene glycol # 300 diacrylate, polyethylene glycol. # 400 diacrylate, polyethylene glycol # 600 diacrylate, alkylphenoxy polyethylene glycol acrylate, N, N-dimethylaminoethyl acrylate, N, N-dimethylaminoethyl methacrylate, Water-soluble vinyl monomers such as N-vinylpyrrolidone, morpholine acrylate, and morpholinoethyl acrylate are included, and the viscosity is 150 cps.
(25 ° C) or less is preferable, and 100 cps (25
C.) or less is more preferable.

【0010】(3)の光重合開始剤は,ジェトキシアセ
トフェノン,ヒドロキシアセトフェノン,α−アミノア
セトフェノンなどアセトフェノン系,ベンゾインエチル
エ−テル,ベンジルジメチルケタ−ルなどベンゾイン
系,ベンゾフェノンなどベンゾフェノン系,2,4 −ジエ
チルチオキサンソンなどチオキサンソン系,メチルフェ
ニルグリオキシレ−ト,アシルホスフィンオキサイドな
どの単独使用又は併用使用を行い,特に限定するわけで
はないが,(1)の光重合性ビニ−ルオリゴマ−,
(2)の光重合性ビニ−ルモノマ−と相溶性の良いもの
が好ましい。臭気,黄変性からは常温で,液状のヒドロ
キシアセトフェノンにアシルホスフィンオキサイドを5
0〜60℃で溶解させたものがより好ましい。
Examples of the photopolymerization initiator (3) include acetophenone-based compounds such as jetoxyacetophenone, hydroxyacetophenone and α-aminoacetophenone, benzoin-based compounds such as benzoinethyl ether and benzyldimethylketane, benzophenone-based compounds such as benzophenone, 2, A thioxanthone compound such as 4-diethylthioxanthone, methylphenylglyoxylate, an acylphosphine oxide, etc. may be used alone or in combination. The photopolymerizable vinyl oligomer of (1) is not particularly limited. ,
Those having good compatibility with the photopolymerizable vinyl monomer (2) are preferable. From odor and yellowing, at room temperature, acylphosphine oxide should be added to liquid hydroxyacetophenone.
What was melt | dissolved at 0-60 degreeC is more preferable.

【0011】(4)の重合禁止剤は,ハイドロキノン,
ハイドロキノンモノメチルエ−テル,モノ−tブチルハ
イドロキノン及びフェノチアジン,カテコ−ルなど周知
のものが挙げられる。
The polymerization inhibitor (4) is hydroquinone,
Known examples include hydroquinone monomethyl ether, mono-t-butyl hydroquinone, phenothiazine and catechol.

【0012】(5)の顔料は,通常の水性インキ用顔
料,例えばモノアゾ系,ジスアゾ系,キナクリドン系,
ナフト−ル系,フタロシアニン系等の有機顔料や二酸化
チタン,硫酸バリウム,炭酸カルシウム,カ−ボンブラ
ック等の無機顔料が使用可能である。
The pigment (5) is an ordinary pigment for water-based ink, for example, a monoazo pigment, a disazo pigment, a quinacridone pigment,
Organic pigments such as naphthol-based and phthalocyanine-based pigments and inorganic pigments such as titanium dioxide, barium sulfate, calcium carbonate and carbon black can be used.

【0013】本発明に使用する水可溶性紫外線硬化型イ
ンキ中の上記物質の配合量は,特に限定されないが,硬
化性,水での洗浄性,1000cps(25℃)以下の
粘度の必要性の点から,(2)の水可溶性モノマ−のイ
ンキ中に占める割合が50〜90重量%の範囲が好まし
い。水可溶性モノマ−が50重量%の以下の場合には,
水での洗浄性が劣り,インキ全体の系の粘度を1000
cps(25℃)以下にするのが困難で,当該印刷方式
に対応出来ない。
The blending amount of the above substances in the water-soluble UV-curable ink used in the present invention is not particularly limited, but it is necessary to have curability, detergency with water and a viscosity of 1000 cps (25 ° C.) or less. Therefore, the proportion of the water-soluble monomer (2) in the ink is preferably in the range of 50 to 90% by weight. If the water-soluble monomer is 50% by weight or less,
Poor detergency with water, the viscosity of the entire ink system is 1000
It is difficult to keep the temperature below cps (25 ° C) and it cannot be applied to the printing method.

【0014】又,(1)の光重合性オリゴマ−は,イン
キ中に占める割合が10〜30重量%の範囲が好まし
い。10重量%以下の場合は硬化性が劣り,30重量%
を超える範囲の場合は粘度を1000cps(25℃)
以下にするのが困難である。(3)の光重合開始剤のイ
ンキ中に占める割合は10重量%以下の範囲で,インキ
を硬化させるに足る割合で使用すれば良い。(4)の重
合禁止剤は,インキの貯蔵安定性を考慮して,0.01
〜0.2重量%の範囲で使用すれば良い。(5)の顔料
のインキに占める割合は8〜20重量%の範囲が好まし
い。
The proportion of the photopolymerizable oligomer (1) in the ink is preferably 10 to 30% by weight. If it is less than 10% by weight, the curability is poor, and 30% by weight
Viscosity is 1000cps (25 ℃)
It is difficult to The proportion of the photopolymerization initiator (3) in the ink is 10% by weight or less, and it may be used in a proportion sufficient to cure the ink. The polymerization inhibitor of (4) is 0.01% in consideration of the storage stability of the ink.
It suffices to use it within a range of up to 0.2% by weight. The proportion of the pigment of (5) in the ink is preferably in the range of 8 to 20% by weight.

【0015】以上の物質を50〜60℃の範囲で周知の
平行型ビ−ズミル(WAB社製ダイノミル,KDL−P
ILOT型,容量1.4リットル)で製造された水可溶
性紫外線硬化型インキは,その粘度が1000cps
(25℃)以下と低粘度のため,表面に微細な凹凸を形
成した主ロ−ルと補助ロ−ルを対向配置し,主ロ−ルに
版胴を接触させて段ボ−ルシ−トに印刷を行う印刷方式
(該フレキソ印刷方式)に対応出来る。又,水及び水可
溶性溶剤を使用していないので,印刷機上での蒸発が無
く粘度上昇を起こさないため,インキを循環させ流動さ
せる必要が無い。その為インキの色替えの際のインキの
無駄を無くすることが出来る。
The above materials are used in the well-known parallel type bead mill (Dyanomill manufactured by WAB Co., Ltd., KDL-P) in the range of 50 to 60 ° C.
The water-soluble UV-curable ink manufactured by ILOT type, capacity 1.4 liters) has a viscosity of 1000 cps.
Because of the low viscosity (25 ° C) or less, the main roll and the auxiliary roll having fine irregularities formed on the surface are arranged opposite to each other, and the plate cylinder is brought into contact with the main roll to form a step ball sheet. It is possible to correspond to a printing method for printing on the same (the flexographic printing method). Further, since neither water nor a water-soluble solvent is used, there is no evaporation on the printing machine and no increase in viscosity occurs, so there is no need to circulate and flow the ink. Therefore, it is possible to eliminate waste of ink when changing colors of ink.

【0016】[0016]

【実施例】 以下、実施例により本発明を具体的に説明
するが、本発明はこれら実施例に限定されるものではな
い。 実施例1.ポリ エステルアクリレート(荒川化学製ビームセット750) 24部 モルホリンアクリレート(興人製 アクモ) 55.95部 ダロキュア−4265(チバガイキ−製光重合開始剤、2-ヒドロキシ-2メチル -1-フェニルプロパン-1-オン。50重量部と2.4.6―トリメチルベンゾイル ジフェニルホスフィンオキサイド50重量部との混合物) 9部 ポリエチレングリコールオクチルフェニルエーテル (第一工業製薬製ノイゲンEA112) 1部 メトキノン(精工化学製ハイドロキシノンモノメチルエーテル) 0.05部 黄色顔料(東洋インキ製リオノ−ルイエロ− SS OW) 10部 合計 100部 上記のような配合物を上述の平行型ビーズミルで混合練
肉して、粘度600cps(25℃)のインキAを得
た。
EXAMPLES Hereinafter, the present invention will be specifically described with reference to examples, but the present invention is not limited to these examples. Example 1. Poly ester acrylate (manufactured by Arakawa Chemical BEAMSET 750) 24 parts morpholine acrylate (Kojin manufactured Akumo) 55.95 parts DAROCUR -4265 (Chibagaiki - manufacturing photopolymerization initiator, 2-hydroxy-2-methyl-1-phenylpropane-1-one A mixture of 50 parts by weight and 2.4.6-trimethylbenzoyldiphenylphosphine oxide 50 parts by weight) 9 parts Polyethylene glycol octyl phenyl ether (Daiichi Kogyo Seiyaku Neugen EA112) 1 part Metoquinone (Hydroxynone monomethyl ether manufactured by Seiko Chemical Co., Ltd.) 0.05 Parts Yellow pigment (Riono-Ruiello-SS OW manufactured by Toyo Ink Co., Ltd.) 10 parts Total 100 parts The above compound was mixed and kneaded in the parallel bead mill to obtain an ink A having a viscosity of 600 cps (25 ° C.). .

【0017】実施例2. 脂肪族エポキシアクリレ−ト(BASF製Laromer LR 8765) 23部 ポリエチレングリコ−ル #300ジアクリレ−ト (第一工業製薬製ニュ−フロンティアPE−300) 31.95部 4-ヒドロキシブチルアクリレ−ト(大阪有機化学工業製4-HBA) 25部 ダロキュア−4265 9部 ノイゲンEA 112 1部 メトキノン 0.05部 リオノ−ルイエロ− SS OW 10部 合計 100部 上記のような配合物をビ−ズミルで混合練肉して,粘度
550cps(25℃)のインキBを得た。
Example 2. Aliphatic epoxy acrylate (BASF Laromer LR 8765) 23 parts Polyethylene glycol # 300 diacrylate (Daiichi Kogyo Seiyaku New Frontier PE-300) 31.95 parts 4-hydroxybutyl acrylate (Osaka Organic Chemical Industry 4-HBA) 25 parts Darocur-4265 9 parts Neugen EA 112 1 part Metoquinone 0.05 parts Rhino-Ruiello-SS OW 10 parts Total 100 parts Mix the above ingredients with a bead mill and knead the mixture. , Ink B having a viscosity of 550 cps (25 ° C.) was obtained.

【0018】実施例3. エポキシアクリレ−ト(荒川化学製 ビ−ム−セットAQ−7) 27部 2−ヒドロキシプロピルアクリレ−ト (共栄社油脂製ライトエステルHOP−A) 52.95部 ダロキュア−4265 9部 ノイゲンEA 112 1部 メトキノン 0.05部 リオノ−ルイエロ− SS OW 10部 合計 100部 上記のような配合物をビ−ズミルで混合練肉して,粘度
440cps(25℃)のインキCを得た。
Example 3. Epoxy acrylate (Beam-Set AQ-7 made by Arakawa Chemical Co., Ltd.) 27 parts 2-Hydroxypropyl acrylate (light ester HOP-A made by Kyoeisha Oil & Fat Co., Ltd.) 52.95 parts Darocur-4265 9 parts Neugen EA 112 1 part Metoquinone 0.05 parts Riono-Ruiello-SS OW 10 parts Total 100 parts The above ingredients were mixed and kneaded in a bead mill to obtain an ink C having a viscosity of 440 cps (25 ° C.).

【0019】実施例4. 塩素化ポリエステルアクリレ−ト(ダイセルUCB製エベクリル584) 23部 モルホリンアクリレ−ト(興人製 アクモ) 32.95部 4-ヒドロキシブチルアクリレ−ト(大阪有機化学工業製4-HBA) 24部 ダロキュア−4265 4.5部 バイキュア55(アクゾ製 光重合開始剤,フェニルグリオキシ酸メチル) 4.5部 ノイゲンEA 112 1部 メトキノン 0.05部 リオノ−ルイエロ− SS OW 10部 合計 100部 上記のような配合物をビ−ズミルで混合練肉して,粘度
660cps(25℃)のインキDを得た。
Example 4. Chlorinated polyester acrylate (Ebecryl 584 made by Daicel UCB) 23 parts Morpholine acrylate (Akmo made by Kojin) 32.95 parts 4-Hydroxybutyl acrylate (4-HBA made by Osaka Organic Chemical Industry) 24 parts Darocure -4265 4.5 parts Vicure 55 (Akzo photopolymerization initiator, methyl phenylglyoxyate) 4.5 parts Neugen EA 112 1 part Metoquinone 0.05 parts Riono-Ruiello-SS OW 10 parts Total 100 parts Ink D having a viscosity of 660 cps (25 ° C.) was obtained by mixing and kneading with a Z-mill.

【0020】比較例1. ポリエステルアクリレ−ト(荒川化学製ビ−ムセット750) 40部 モルホリンアクリレ−ト(興人製 アクモ) 39.95部 ダロキュア−4265 9部 ノイゲンEA 112 1部 メトキノン 0.05部 リオノ−ルイエロ− SS OW 10部 合計 100部 上記のような配合物をビ−ズミルで混合練肉して,粘度
1210cps(25℃)のインキEを得た。
Comparative Example 1. Polyester acrylate (Beam set 750 manufactured by Arakawa Chemical Co., Ltd.) 40 parts Morpholine acrylate (Akmo made by Kojin) 39.95 parts Darocur-4265 9 parts Neugen EA 112 1 part Metoquinone 0.05 parts Riono-Ruiero SS OW 10 parts 100 parts in total The above ingredients were mixed and kneaded with a bead mill to obtain an ink E having a viscosity of 1210 cps (25 ° C.).

【0021】比較例2. モルホリンアクリレ−ト(興人製 アクモ) 79.95部 ダロキュア−4265 9部 ノイゲンEA 112 1部 メトキノン 0.05部 リオノ−ルイエロ− SS OW 10部 合計 100部 上記のような配合物をビ−ズミルで混合練肉して,粘度
400cps(25℃)のインキFを得た。
Comparative Example 2. Morpholine Acrylate (Akmo made by Kojin) 79.95 parts Darocur-4265 9 parts Neugen EA 112 1 part Metoquinone 0.05 parts Riono-Ruiello-SS OW 10 parts Total 100 parts Mixing the above-mentioned compounds with a bead mill Ink F was obtained with a viscosity of 400 cps (25 ° C.).

【0022】比較例3.冷却装置付き四ッ口フラスコ
に,粉末状ジアリルフタレ−ト樹脂(ダイソ−製ダイソ
−イソダップ)42重量部とEO変性トリメチロ−ルプ
ロパントリアクリレ−ト(三洋化成製ネオマ−TA40
1)57.95重量部とハイドロキノンモノメチルエ−
テル0.05重量部を入れ,120℃オイルバス中で3
0分間攪拌溶解させた。このようにして得られたものを
ワニス(1)とした。次に,このワニス(1)を用いて
以下の組成でインキを製造した。 ワニス(1) 24部 1.6 ヘキサンジオ−ルジアクリレ−ト (共栄社油脂製ライトアクリレ−ト1.6 HX−A) 55.95部 ダロキュア4265 9部 ノイゲンEA−112 1部 メトキノン 0.05部 リオノ−ルイエロ− SS OW 10部 合計 100部 上記のような配合物をビ−ズミルで混合練肉して,粘度
390cps(25℃)のインキGを得た。
Comparative Example 3. In a four-necked flask equipped with a cooling device, 42 parts by weight of powdered diallyl phthalate resin (Daiso-Isodap manufactured by Daiso) and EO-modified trimethylolpropane triacrylate (Neoma-TA40 manufactured by Sanyo Kasei Co., Ltd.) were used.
1) 57.95 parts by weight of hydroquinone monomethyl ether
Add 0.05 parts by weight of tellurium and put in an oil bath at 120 ℃ for 3
It was dissolved by stirring for 0 minutes. The product thus obtained was used as varnish (1). Next, an ink having the following composition was produced using this varnish (1). Varnish (1) 24 parts 1.6 Hexanediol diacrylate (Kyoeisha Oil and Fat Light Acrylate 1.6 HX-A) 55.95 parts Darocur 4265 9 parts Neugen EA-112 1 part Metoquinone 0.05 parts Riono-Ruiello-SS OW 10 parts Total 100 parts The above mixture was mixed and kneaded with a bead mill to obtain an ink G having a viscosity of 390 cps (25 ° C.).

【0023】比較例4. スチレンアクリル共重合体樹脂 12部 ロジンマレイン酸樹脂 8部 水 15部 アクリルエマルジョン 20部 エチレングリコ−ル 30部 ジエタノ−ルアミン 2部 ポリエチレンワックス 3部 リオノ−ルイエロ− SS OW 10部 合計 100部 上記のような組成で,現在従来技術の方法で製造され,
実用化されているインキを,インキHとした。Hの粘度
は,440cps(25℃)であった。
Comparative Example 4. Styrene acrylic copolymer resin 12 parts Rosin maleate resin 8 parts Water 15 parts Acrylic emulsion 20 parts Ethylene glycol 30 parts Diethanolamine 2 parts Polyethylene wax 3 parts Riono-Ruiello-SS OW 10 parts Total 100 parts As above Of different composition, currently manufactured by prior art methods,
The ink that has been put into practical use is called ink H. The viscosity of H was 440 cps (25 ° C.).

【0024】以上のようにして製造された8種のインキ
A〜Hを,以下の方法で印刷及び評価テストを行い,表
1に示すような結果を得た。印刷機は,ISOWA製造
及び新機械製フレキソ印刷機を用い,165線/イン
チのアニロックスロールを使い,印刷スピード60
分で印刷を行った。段ボールシートは,十条製紙白ライ
ナー180g/m及びプラスチック段ボール三井東圧
製パロニヤ(処理PP)を使用した。
The eight kinds of inks A to H produced as described above were printed and evaluated by the following methods, and the results shown in Table 1 were obtained. Printing machine, using ISOWA production and new Saiwai Machine flexographic printing machine, using the anilox roll 165 lines / inch, printing speed 60 sheets /
Printed in minutes. As the corrugated cardboard sheet, 180 g / m 2 of Jujo Paper White Liner and PALONYA (treated PP) manufactured by Mitsui Toatsu Co., Ltd. were used.

【0025】このようにして得られた印刷物に出力12
0W/cmのメタルハライドランプを使用してラインス
ピ−ド20m/分,照射距離10.8cmでインキが指
につかなくなるまで照射ラインを通過させ,硬化性の判
定を行った。又,粘度上昇についての評価はデジタルイ
ンコメ−タ−(東洋精機製)400rpm循環水温32
℃で10分間回転させ,10分間後のタック値と1分間
後の差で上昇の度合いを判定した。印刷適性は,アニロ
ックスロ−ラ−と対向ロ−ラ−間でのインキの絞り(イ
ンキ膜厚の調整)が良好か否かで判断した。
The printed matter thus obtained is output 12
A 0 W / cm metal halide lamp was used to pass the irradiation line at a line speed of 20 m / min and an irradiation distance of 10.8 cm until the ink did not stick to the finger, and the curability was determined. In addition, the evaluation of the viscosity increase was performed by digital incomer (manufactured by Toyo Seiki) 400 rpm circulating water temperature 32.
Rotation was carried out at 0 ° C. for 10 minutes, and the degree of increase was judged by the tack value after 10 minutes and the difference after 1 minute. The printability was judged by whether or not the ink squeezing (adjusting the ink film thickness) between the anilox roller and the counter roller was good.

【0026】[0026]

【表1】 [Table 1]

【0027】[0027]

【発明の効果】【The invention's effect】

(1)インキが無溶剤なので従来技術の方法で製造さ
れ,実用化されているインキのように蒸発が無い為,印
刷機上で粘度上昇が無く,インキを絶えず循環流動させ
る必要が無い為,インキ供給システムを簡素化出来る。
又アルコ−ルなど蒸発物質を共用していないので,昨今
厳しくなっている環境汚染を防止することが出来る。 (2)紫外線硬化型のインキを使用する為に,一般のラ
イナ−紙以外に撥水ライナ−,樹脂コ−トライナ−、フ
ィルムラミネ−トライナ−,処理プラスチック段ボ−ル
への印刷も可能である。 (3)本発明のインキは,水可溶性を有しいる為,印刷
装置の洗浄は水を使用することが可能である。 (4)印刷面は紫外線を照射することにより瞬時に乾燥
し,次の工程が連続して行われ,生産性の向上と生産コ
ストの低減が可能になる。
(1) Since the ink is solvent-free, it does not evaporate like the ink produced by the conventional technology and put into practical use, so there is no increase in viscosity on the printing machine and there is no need to constantly circulate the ink. The ink supply system can be simplified.
Moreover, since the evaporation material such as alcohol is not shared, it is possible to prevent the environmental pollution which has become severe these days. (2) Since UV-curable ink is used, printing on water-repellent liner, resin coat liner, film laminar liner, treated plastic corrugated ball is also possible in addition to general liner paper. is there. (3) Since the ink of the present invention is water-soluble, it is possible to use water for cleaning the printing device. (4) The printed surface is instantly dried by irradiating with ultraviolet rays, and the next step is continuously performed, which makes it possible to improve productivity and reduce production cost.

───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.7,DB名) C09D 11/02 C09D 11/10 ─────────────────────────────────────────────────── ─── Continuation of front page (58) Fields surveyed (Int.Cl. 7 , DB name) C09D 11/02 C09D 11/10

Claims (3)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 表面に微細な凹凸を形成した主ロール
(アニロックスロール)と、補助ロールを対向配置
し、主ロールに版銅を接触させて被印刷物に印刷する
レキソ印刷方式に用いられる水可溶性紫外線硬化型イン
キにおいて、 前記水可溶性紫外線硬化型インキは、水可溶性成分を5
0〜100重量%含み、インキ粘度が1000cps
(25℃)以下であって、 水及び水可溶性溶剤を含まな
いことを特徴とする水可溶性紫外線硬化型インキ。
1. A main roll forming a fine uneven surface (the anilox roll), and an auxiliary roll arranged opposite to printed on a substrate by contacting the Bando to main roll off
Water-soluble UV-curable ink used for lexographic printing
In G., the water-soluble UV-curable ink contains 5 parts of water-soluble components.
Including 0 to 100% by weight, ink viscosity is 1000 cps
A water-soluble UV-curable ink having a temperature of (25 ° C.) or less and containing neither water nor a water-soluble solvent.
【請求項2】 前記水可溶性紫外線硬化型インキは、
外線を照射することにより重合硬化する水可溶性ビニー
ルオリゴマー、水可溶性ビニールモノマー、光重合開始
剤、重合禁止剤、顔料を主成分とする混合物よりなるこ
とを特徴とする請求項1に記載の水可溶性紫外線硬化型
インキ。
Wherein said water soluble ultraviolet curable inks, water-soluble Binney <br/> Le oligomer polymerized and cured by irradiation with ultraviolet rays, water-soluble vinyl monomer, a photopolymerization initiator, a polymerization inhibitor, a pigment main The water-soluble UV-curable ink according to claim 1, which is composed of a mixture of components.
【請求項3】 前記水可溶性紫外線硬化型インキは、粘
度が150cps(25℃)以下の水可溶性ビニルモノ
マーを50〜90重量%含むことを特徴とする請求項2
に記載の水可溶性紫外線硬化型インキ。
3. The water-soluble UV-curable ink is a viscous ink.
Water-soluble vinyl mono with a degree of less than 150 cps (25 ° C)
Mar of 50-90% by weight.
The water-soluble ultraviolet-curable ink according to item 1.
JP01487794A 1994-01-12 1994-01-12 UV curable ink for printing stepped ball sheets Expired - Fee Related JP3366716B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP01487794A JP3366716B2 (en) 1994-01-12 1994-01-12 UV curable ink for printing stepped ball sheets

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP01487794A JP3366716B2 (en) 1994-01-12 1994-01-12 UV curable ink for printing stepped ball sheets

Publications (2)

Publication Number Publication Date
JPH07207208A JPH07207208A (en) 1995-08-08
JP3366716B2 true JP3366716B2 (en) 2003-01-14

Family

ID=11873250

Family Applications (1)

Application Number Title Priority Date Filing Date
JP01487794A Expired - Fee Related JP3366716B2 (en) 1994-01-12 1994-01-12 UV curable ink for printing stepped ball sheets

Country Status (1)

Country Link
JP (1) JP3366716B2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5938826A (en) * 1997-05-16 1999-08-17 Markem Corporation Hot melt ink
JP4260846B2 (en) * 2007-02-07 2009-04-30 株式会社セイコーアドバンス UV curable ink for screen printing, decorative prints and decorative resin moldings
JP2009057571A (en) * 2008-10-24 2009-03-19 Seiko Advance:Kk Ultraviolet-curing ink, decorated printed matter, and decorated resin molding
JP6302362B2 (en) * 2014-06-13 2018-03-28 花王株式会社 Flexographic ink

Also Published As

Publication number Publication date
JPH07207208A (en) 1995-08-08

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