JPH05171087A - Water-base flexographic ink composition - Google Patents
Water-base flexographic ink compositionInfo
- Publication number
- JPH05171087A JPH05171087A JP35512791A JP35512791A JPH05171087A JP H05171087 A JPH05171087 A JP H05171087A JP 35512791 A JP35512791 A JP 35512791A JP 35512791 A JP35512791 A JP 35512791A JP H05171087 A JPH05171087 A JP H05171087A
- Authority
- JP
- Japan
- Prior art keywords
- water
- resin
- ink
- weight
- ink composition
- 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.)
- Pending
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 15
- 229920005989 resin Polymers 0.000 claims abstract description 47
- 239000011347 resin Substances 0.000 claims abstract description 47
- 150000001875 compounds Chemical class 0.000 claims abstract description 21
- 239000004593 Epoxy Substances 0.000 claims abstract description 11
- 239000013522 chelant Substances 0.000 claims abstract description 8
- 229910052751 metal Inorganic materials 0.000 claims abstract description 8
- 239000002184 metal Substances 0.000 claims abstract description 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- 239000003849 aromatic solvent Substances 0.000 abstract description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 39
- 239000000976 ink Substances 0.000 description 35
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 12
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 12
- 239000004698 Polyethylene Substances 0.000 description 11
- 229920000573 polyethylene Polymers 0.000 description 11
- 239000000123 paper Substances 0.000 description 9
- -1 polyethylene Polymers 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 7
- 239000011248 coating agent Substances 0.000 description 7
- 238000000576 coating method Methods 0.000 description 7
- 238000010030 laminating Methods 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 239000000853 adhesive Substances 0.000 description 6
- 230000001070 adhesive effect Effects 0.000 description 6
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 6
- 239000000049 pigment Substances 0.000 description 6
- 238000012805 post-processing Methods 0.000 description 6
- 150000002902 organometallic compounds Chemical class 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 229920006026 co-polymeric resin Polymers 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 235000011114 ammonium hydroxide Nutrition 0.000 description 3
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical group C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 2
- 239000004606 Fillers/Extenders Substances 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 238000007774 anilox coating Methods 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 235000010187 litholrubine BK Nutrition 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 2
- WTYYGFLRBWMFRY-UHFFFAOYSA-N 2-[6-(oxiran-2-ylmethoxy)hexoxymethyl]oxirane Chemical compound C1OC1COCCCCCCOCC1CO1 WTYYGFLRBWMFRY-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- QCEXHNUBYGLRHV-UHFFFAOYSA-L C(C)CC(=O)[O-].C(C)CC(=O)[O-].C(CC)O[Ti+2]OCCC Chemical compound C(C)CC(=O)[O-].C(C)CC(=O)[O-].C(CC)O[Ti+2]OCCC QCEXHNUBYGLRHV-UHFFFAOYSA-L 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 1
- FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical compound C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- XRASGLNHKOPXQL-UHFFFAOYSA-L azane 2-oxidopropanoate titanium(4+) dihydrate Chemical compound N.N.O.O.[Ti+4].CC([O-])C([O-])=O.CC([O-])C([O-])=O XRASGLNHKOPXQL-UHFFFAOYSA-L 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000002301 combined effect Effects 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000003851 corona treatment Methods 0.000 description 1
- 239000013530 defoamer Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- UTSYWKJYFPPRAP-UHFFFAOYSA-N n-(butoxymethyl)prop-2-enamide Chemical compound CCCCOCNC(=O)C=C UTSYWKJYFPPRAP-UHFFFAOYSA-N 0.000 description 1
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- ARJOQCYCJMAIFR-UHFFFAOYSA-N prop-2-enoyl prop-2-enoate Chemical compound C=CC(=O)OC(=O)C=C ARJOQCYCJMAIFR-UHFFFAOYSA-N 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 150000003609 titanium compounds Chemical class 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
Landscapes
- Inks, Pencil-Leads, Or Crayons (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、紙及びプラスチック・
フィルムに用いられる水性フレキソインキ組成物に関す
るものであり、特にラミネート印刷構成物を作成すると
きに1液型で安定で刷り易いインキであって、ポリオレ
フィンフィルムのラミネート貼り合せ時の接着強度の低
下もなく、後加工で使用される芳香族系溶剤、特にトル
エンに対して、耐性の優れたインキ膜を提供する水性フ
レキソインキ組成物である。BACKGROUND OF THE INVENTION The present invention relates to paper and plastics.
The present invention relates to a water-based flexo ink composition used for a film, which is a stable, easy-to-print ink in a one-component type when a laminated printing composition is prepared, and also reduces the adhesive strength when laminating and laminating a polyolefin film. And an aqueous flexo ink composition that provides an ink film having excellent resistance to an aromatic solvent used in post-processing, particularly toluene.
【0002】従来、水性フレキソインキは、分散型樹脂
を主要樹脂としたものが多く、インキ塗膜物性には優れ
ると言われているが、印刷適性特にアニロックスロール
の目詰りや版上のインキ転移性不良にもとづく版かぶり
等が問題となっている。一般に高酸価の樹脂とすること
で耐トルエン性は向上するが、樹脂の安定性や製造の容
易さから高酸価樹脂を合成する時、芳香族系モノマー
(主にスチレン、又はその誘導体)を共重合とすること
からこの樹脂をベースとした水性フレキソ1液型インキ
ではトルエン耐性を得るのは困難であった。一方、水溶
性樹脂の場合は、酸価と分子量を調節して水溶化を行う
が、希釈安定性、印刷粘度から酸価と分子量が限定され
る。それゆえ、水溶性樹脂を用いる水性フレキソインキ
から得られるインキ皮膜のトルエン耐性は貧弱である。
さらにポリエチレンエクストルージョン加工やプルタプ
紙(ポリエチレンと紙との貼合紙)との熱圧着による熱
時での接着強度は、上記2種の水溶性樹脂および水分散
型樹脂をベースとした水性フレキソ1液型インキでは困
難である。[0002] Conventionally, water-based flexo inks are mainly composed of a dispersion type resin as a main resin, and it is said that they are excellent in the physical properties of an ink coating film. However, their printability, especially clogging of anilox rolls and ink transfer on a plate. Fogging of plates due to poor quality is a problem. Toluene resistance is generally improved by using a resin with a high acid value, but aromatic monomers (mainly styrene or its derivatives) are used when synthesizing a resin with a high acid value due to the stability of the resin and the ease of manufacture. It is difficult to obtain toluene resistance in the aqueous flexo one-pack type ink based on this resin because of the copolymerization. On the other hand, in the case of a water-soluble resin, the acid value and molecular weight are adjusted for water-solubilization, but the acid value and molecular weight are limited due to dilution stability and printing viscosity. Therefore, the toluene resistance of the ink film obtained from the water-based flexo ink using the water-soluble resin is poor.
Furthermore, the adhesive strength under heat due to polyethylene extrusion processing or thermal compression bonding with pull-tap paper (bonding paper of polyethylene and paper) is based on the above-mentioned two types of water-soluble resin and water-dispersible resin. Difficult with liquid ink.
【0003】水性フレキソインキ印刷物の溶融ポリエチ
レンによる貼合せ時において、従来からインキ印刷部分
の安定なラミネート強度を得ることが困難であった。又
印刷適性を保持する1液型インキにおいて、後加工に用
いられる芳香族系溶剤で塗膜が膨潤し、ラミ強度が低下
するのを防ぐことは困難であった。本発明者らは検討の
結果、金属キレート化合物とエポキシ化合物がpHが7
以上の領域で、低温熱処理によって架橋結合を形成する
ことで、安定なラミネート強度を保持し、後加工に用い
られる芳香族系溶剤でも耐性のある塗膜を形成すること
を見い出しこのメカニズムを水性フレキソインキに適用
することで、これら問題点を解決するに至ったものであ
る。When laminating a water-based flexographic ink print with molten polyethylene, it has hitherto been difficult to obtain a stable laminate strength in the ink-printed portion. Further, in the one-pack type ink which maintains the printability, it is difficult to prevent the coating film from swelling due to the aromatic solvent used for the post-processing and the deterioration of the laminating strength. As a result of investigations by the present inventors, the metal chelate compound and the epoxy compound have a pH of 7
In the above areas, it was found that forming a cross-link bond by low temperature heat treatment maintains stable laminate strength and forms a coating film that is resistant to aromatic solvents used for post-processing. By applying it to ink, these problems have been solved.
【0004】本発明は、印刷適性に優れ、且つ芳香族溶
剤を用いた加工剤による後加工でも、ラミネート強度の
低下もなく、インキ皮膜の耐性に優れた水性フレキソイ
ンキに関するもので、その構成は水溶性樹脂と水分散型
樹脂混合系を主要な水性インキ樹脂とし、インキのpH
を7以上とし、金属キレート化合物1〜5重量%と、エ
ポキシ化合物1〜10重量%を含有することを特徴とす
る水性フレキソインキ組成物である。The present invention relates to a water-based flexo ink which has excellent printability, has no deterioration in laminate strength even after processing with a processing agent using an aromatic solvent, and has excellent ink film resistance. The water-soluble resin and water-dispersible resin mixed system is the main water-based ink resin, and the pH of the ink is
Is 7 or more, and 1 to 5% by weight of the metal chelate compound and 1 to 10% by weight of the epoxy compound are contained, which is an aqueous flexo ink composition.
【0005】印刷適性、特に版かぶりやアニロックスロ
ールのセル目詰り防止には水溶性樹脂が効果的である。
しかし耐水性が低下のため分散型樹脂の併用が最も実用
的な骨格樹脂成分となる。A water-soluble resin is effective for printability, especially for preventing plate fogging and cell clogging of anilox roll.
However, since the water resistance is lowered, the combined use of the dispersion type resin becomes the most practical skeleton resin component.
【0006】以下実用のケースについて述べる。先づ紙
へ水性フレキソインキによって印刷後、乾燥し、イン・
ライン加工でコロナ放電処理を行ってからポリエチレン
(PE)のエクストルージョンラミで印刷面とPEとを
貼り合る。その後、後加工としてシリコン溶解トルエン
溶液をPE面に塗布乾燥し、その上に粘着剤トルエン溶
液を塗工し、巻き取ることにより水性フレキソ印刷した
紙テープの加工は終る。使用時においては、シリコンの
作用により粘着剤が紙に転移し紙テープとしての機能を
果たす。後加工と言うのはPE貼り合せ後の面にシリコ
ンのトルエン溶液を塗工して、乾燥後再び溶剤型粘着剤
を塗工する工程を指す。これらの工程で用いられるトル
エンがポリエチレンフィルムとの貼り合せ界面や、紙の
裏面から浸透し、印刷インキの塗膜を犯すことで問題が
発生する。A practical case will be described below. First, print on paper with water-based flexo ink, dry,
After the corona discharge treatment is performed by line processing, the printed surface and the PE are attached to each other by the extrusion laminating of polyethylene (PE). Thereafter, as a post-processing, a silicon-dissolved toluene solution is applied to the PE surface and dried, and then an adhesive toluene solution is applied onto the PE surface and wound up to finish the processing of the aqueous flexographically printed paper tape. At the time of use, the adhesive acts on the paper by the action of silicon to function as a paper tape. The post-processing refers to the step of applying a toluene solution of silicon to the surface after the PE bonding, drying and then applying the solvent-based adhesive again. A problem occurs when toluene used in these steps penetrates from the bonding interface with the polyethylene film or from the back surface of the paper and violates the coating film of the printing ink.
【0007】主要樹脂成分としての水溶性樹脂および水
分散型樹脂は、該樹脂がカルボキル基および/または水
酸基を含有していれば何等制限はない。The water-soluble resin and the water-dispersible resin as main resin components are not limited as long as the resin contains a carboxyl group and / or a hydroxyl group.
【0008】金属キレート化合物の役割は、樹脂中のカ
ルボキシル基への配位と併用のエポキシ樹脂化合物の開
環による水酸基との架橋形成によって、熱可ソ性樹脂の
高温度での熔融による結晶化のくずれを補って樹脂皮膜
に靱性を付与するものである。The role of the metal chelate compound is to coordinate to the carboxyl group in the resin and to form a crosslink with the hydroxyl group by ring opening of the epoxy resin compound used in combination, so that the heat-curable resin is crystallized by melting at a high temperature. It compensates for the collapse of the resin and imparts toughness to the resin film.
【0009】金属キレート化合物としては次のものが用
いられる。有機のチタン化合物や有機のアルミニウム化
合物がある。代表的な例としたは、テトライソプロピル
チタネート、ジヒドロキシ−ビス(ラクテート)、チタ
ンラクテートアンモニウム塩、ジプロポキシチタン−ビ
ス(エチルアセテート)、トリプロポキシアルミニウ
ム、ジプロポキシアルミ−エチルアセテート等である。
その使用量の範囲は1〜5重量%である。1%未満の時
は、殆んど効果を示さず、熱時、ラミ強度の安定化には
役立たない。また、5重量%を超える場合においては、
インキの安定性をそこなうため好ましくない。The following compounds are used as the metal chelate compound. There are organic titanium compounds and organic aluminum compounds. Typical examples are tetraisopropyl titanate, dihydroxy-bis (lactate), titanium lactate ammonium salt, dipropoxytitanium-bis (ethyl acetate), tripropoxyaluminum, dipropoxyaluminum-ethylacetate and the like.
The range of the amount used is 1 to 5% by weight. When it is less than 1%, almost no effect is exhibited, and it is not useful for stabilizing the laminating strength during heating. When it exceeds 5% by weight,
Ink stability is impaired, which is not preferable.
【0010】併用エポキシ樹脂の役割は金属キレート化
合物単独では耐トルエン耐性の向上は殆んどなく、併用
により始めてインキ塗膜の耐性が向上し、ラビングテス
トやセロテープ剥離の評価でその効果を簡便数値化評価
出来、本機でもその再現性を得ている。The role of the combined epoxy resin is that the metal chelate compound alone hardly improves the resistance to toluene, and the combined use improves the resistance of the ink coating film for the first time, and the effect is easily evaluated by the rubbing test and the evaluation of cellophane tape. It is possible to evaluate it, and the reproducibility is obtained with this machine.
【0011】尚インキ中のpH>7のとき、熱処理(エ
クストルージョン時の熱又はPEコートのプルタブ紙の
熱圧着時)で、エポキシ化合物と金属キレート化合物と
の反応が進行しやすいエポキシ化合物としては以下のも
のが用いられる。ビスフェノール骨格を有する両端グリ
シジル基とトリメチロールプロパンとの反応物、ビスフ
ェノール骨格を有する両端のグリシジル基とグリセリン
との反応物、ラウリルアルコールエチレンオキサイド付
加物とグリシジル基との反応物、ソルビトールポリグリ
シジルエーテル、1,6ヘキサンジオールジグリシジル
エーテル、フェニルグリシジルエーテル、ビスフェノー
ルチオジグリシジルエーテル、アクリルグリシジルエー
テル、等である。When pH> 7 in the ink, as an epoxy compound in which the reaction between the epoxy compound and the metal chelate compound easily proceeds by heat treatment (heat during extrusion or thermocompression bonding of PE-coated pull-tab paper) The following are used: Reaction product of glycidyl group having both ends with bisphenol skeleton and trimethylolpropane, reaction product of glycidyl group having both ends having bisphenol skeleton and glycerin, reaction product of lauryl alcohol ethylene oxide adduct and glycidyl group, sorbitol polyglycidyl ether, 1,6 hexanediol diglycidyl ether, phenyl glycidyl ether, bisphenol thiodiglycidyl ether, acryl glycidyl ether, and the like.
【0012】その併用量は1〜10重量%で好ましくは
2〜5重量%である。1%より少ない時はその併用効果
は認められず、又10%を越える時はインキの安定性、
粘度変化などで好ましくない。The amount used in combination is 1 to 10% by weight, preferably 2 to 5% by weight. When it is less than 1%, the combined effect is not recognized, and when it exceeds 10%, the stability of the ink is
It is not preferable because of changes in viscosity.
【0013】[0013]
【実施例】以下、実施例により、本発明を具体的に説明
するが、本発明は以下の実施例に限られるものではな
い。EXAMPLES The present invention will be specifically described below with reference to examples, but the present invention is not limited to the following examples.
【0014】水分散型樹脂(a)の製造 500mlの4口フラスコ中にスチレン/アクリルアク
リレート共重合体樹脂溶液(酸化200、固形分30重
量%、pH8.2)100gを仕込む。次いで、pH
8.5に調整したアンモニア水40g、過硫酸アンモニ
ウム1gを攪拌、溶解させ70℃する。70℃になった
とき2エチルヘキシルアクリレート/メチルメタアクリ
レート=50/50の混合物60gを攪拌しながら60
分間かけて滴下し、さらに過硫酸アンモニウム(10重
量%水溶液)を3ml加え、2時間70〜80℃に保ち
反応を終了させた。上記にて得られた水分散型樹脂
(a)は、酸化67、固形分30重量%、pH8.5、
粘度850mPaであった。Production of Water-Dispersible Resin (a) 100 g of a styrene / acryl acrylate copolymer resin solution (oxidized 200, solid content 30% by weight, pH 8.2) is charged into a 500 ml four-necked flask. Then pH
Ammonia water (40 g) adjusted to 8.5 and ammonium persulfate (1 g) are stirred and dissolved to 70 ° C. When the temperature reached 70 ° C., 60 g of a mixture of 2 ethylhexyl acrylate / methyl methacrylate = 50/50 was stirred and 60
After dropwise addition for 3 minutes, 3 ml of ammonium persulfate (10% by weight aqueous solution) was added, and the reaction was terminated by keeping the temperature at 70 to 80 ° C. for 2 hours. The water-dispersible resin (a) obtained above was oxidized 67, solid content 30% by weight, pH 8.5,
The viscosity was 850 mPa.
【0015】水分散型樹脂(b)の製造 500mlの4口フラスコ中にスチレン/アクリルアク
リレート/β−ヒドロキシルメタアクリレート=63/
27/10の共重合体樹脂溶液(酸化210、固形分3
0重量%、pH8.5)100gを仕込む。次いで、p
H8.5に調整したアンモニア水40g、過硫酸アンモ
ニウム1gを攪拌、溶解させ70℃する。70℃になっ
たときスチレン/メチルメタアクリレート/2エチルヘ
キシルアクリレート=50/30/20の混合物120
gを攪拌しながら90分間かけて滴下し、さらに過硫酸
アンモニウム(10重量%水溶液)を10ml加え、2
時間70〜80℃に保ち反応を終了させた。上記にて得
られた水分散型樹脂(b)は、酸化42、固形分45.
5重量%、pH8.5、粘度300mPaであった。Preparation of water-dispersible resin (b) Styrene / acrylic acrylate / β-hydroxyl methacrylate = 63 / in a 500 ml four-necked flask.
27/10 copolymer resin solution (oxidation 210, solid content 3
100 g of 0% by weight, pH 8.5 is charged. Then p
40 g of ammonia water adjusted to H8.5 and 1 g of ammonium persulfate are stirred and dissolved to 70 ° C. A mixture of styrene / methyl methacrylate / 2 ethylhexyl acrylate = 50/30/20 at 70 ° C. 120
g with stirring over 90 minutes, 10 ml of ammonium persulfate (10% by weight aqueous solution) was added, and 2 g was added.
The reaction was terminated by keeping the temperature at 70 to 80 ° C. The water-dispersible resin (b) obtained above had an oxidation of 42 and a solid content of 45.
It was 5% by weight, pH 8.5, and viscosity 300 mPa.
【0016】水分散型樹脂(c)の製造 500mlの4口フラスコ中にスチレン/メチルメタア
クリレート/アクリルアクリレート/N−ブトキシメチ
ルアクリルアミド=15/45/30/10の共重合体
樹脂溶液(酸化210、固形分30重量%、pH8.
5)100gを仕込む。次いで、pH8.5に調整した
アンモニア水40g、過硫酸アンモニウム1gを攪拌、
溶解させ70℃する。70℃になったとき2エチルヘキ
シルアクリレート/2エチルヒドロキシアクリレート/
メチルメタアクリレート=30/30/40の混合物6
0gを攪拌しながら90分間かけて滴下し、さらに過硫
酸アンモニウム(10重量%水溶液)を3ml加え、2
時間70〜80℃に保ち反応を終了させた。上記にて得
られた水分散型樹脂(c)は、酸化70、固形分45.
5重量%、pH8.5、粘度300mPaであった。Preparation of water-dispersible resin (c) A copolymer resin solution of styrene / methyl methacrylate / acrylic acrylate / N-butoxymethyl acrylamide = 15/45/30/10 (oxidation 210 , Solid content 30% by weight, pH 8.
5) Charge 100 g. Then, 40 g of ammonia water adjusted to pH 8.5 and 1 g of ammonium persulfate are stirred,
Melt and heat to 70 ° C. 2 ethylhexyl acrylate / 2 ethyl hydroxy acrylate /
Mixture 6 of methyl methacrylate = 30/30/40
0 g was added dropwise with stirring over 90 minutes, and 3 ml of ammonium persulfate (10% by weight aqueous solution) was added, and 2 g was added.
The reaction was terminated by keeping the temperature at 70 to 80 ° C. The water-dispersible resin (c) obtained above had an oxidation of 70 and a solid content of 45.
It was 5% by weight, pH 8.5, and viscosity 300 mPa.
【0017】実施例1 水分散型樹脂(a) 0.4部 顔料(カーミン6B) 16.0部 体質顔料(炭酸カルシュム) 5.0部 アニオン系活性剤 0.6部 水 24.9部 上記組成物をレッドテビルにて顔料の高濃度分散体水溶
液を作る。次いで得られた高濃度分散体水溶液に下記組
成物および表1に示す有機金属化合物、エポキシ化合物
を添加し、水性フレキソインキを得た。 水溶性樹脂 (スチレン/アクリルアクリレート共重合体樹脂溶液 酸化20 0、固形分30重量%、pH8.2) 42.0部 水分散ワックス 1.6部 消泡剤 0.9部 イソプロピルアルコール 4.0部 得られた水性フレキソインキをクラフト紙にアプリケー
ターにて塗工し、60℃にて5分間乾燥を行った。塗膜
の耐トルエン性としてラビング試験および滴下試験を行
い結果を表2に示す。 ラビング試験方法 脱脂綿にトルエンを含ませ、印刷物をラビングし、脱脂
綿に着色したときの回数を求めた。 滴下試験 印刷物にトルエンを滴下し、インキ塗膜の溶ける度合い
を評価した。 5:全く溶解しなかった。 4:0〜20%以下が溶解した。 3:20〜50%以下が溶解した。 2:50〜70%以下が溶解した。 1:70%以上が溶解した。Example 1 Water-dispersible resin (a) 0.4 part Pigment (Carmine 6B) 16.0 parts Extender pigment (calcium carbonate) 5.0 parts Anionic activator 0.6 parts Water 24.9 parts The composition is made into a concentrated pigment aqueous solution with Red Tevir. Next, the following composition and the organometallic compound and epoxy compound shown in Table 1 were added to the obtained high-concentration dispersion aqueous solution to obtain an aqueous flexo ink. Water-soluble resin (styrene / acrylic acrylate copolymer resin solution 200, solid content 30% by weight, pH 8.2) 42.0 parts Water-dispersed wax 1.6 parts Defoamer 0.9 parts Isopropyl alcohol 4.0 The obtained aqueous flexo ink was applied to kraft paper with an applicator and dried at 60 ° C. for 5 minutes. A rubbing test and a dropping test were conducted as the toluene resistance of the coating film, and the results are shown in Table 2. Rubbing Test Method The absorbent cotton was made to contain toluene, and the printed matter was rubbed to determine the number of times when the absorbent cotton was colored. Dropping test Toluene was dropped onto the printed matter to evaluate the degree of dissolution of the ink coating film. 5: It did not dissolve at all. 4: 0 to 20% or less dissolved. 3: 20-50% or less melt | dissolved. 2: 50-70% or less melt | dissolved. 1: 70% or more dissolved.
【0018】実施例2 実施例1にて用いた水分散型樹脂(a)を水分散型樹脂
(b)にかえ、表1に示す有機金属化合物、エポキシ化
合物を添加し、それ以外は実施例1と同様にして水性フ
レキソインキを作成し、同様の評価を行い、その結果を
表2に示す。Example 2 The water-dispersible resin (a) used in Example 1 was replaced with the water-dispersible resin (b), and the organometallic compounds and epoxy compounds shown in Table 1 were added. A water-based flexo ink was prepared in the same manner as in Example 1 and evaluated in the same manner. The results are shown in Table 2.
【0019】実施例3 実施例1にて用いた水分散型樹脂(a)を水分散型樹脂
(c)にかえ、表1に示す有機金属化合物、エポキシ化
合物を添加し、それ以外は実施例1と同様にして水性フ
レキソインキを作成し、同様の評価を行い、その結果を
表2に示す。Example 3 The water-dispersible resin (a) used in Example 1 was replaced with the water-dispersible resin (c), and the organometallic compounds and epoxy compounds shown in Table 1 were added. A water-based flexo ink was prepared in the same manner as in Example 1 and evaluated in the same manner. The results are shown in Table 2.
【0020】比較例1 水分散型樹脂(a) 0.4部 顔料(カーミン6B) 16.0部 体質顔料(炭酸カルシュム) 5.0部 アニオン系活性剤 0.6部 水 24.9部 上記組成物をレッドテビルにて顔料の高濃度分散体水溶
液を作る。次いで得られた高濃度分散体水溶液に下記組
成物および表1に示す有機金属化合物、エポキシ化合物
を添加し、水性フレキソインキを得た。以下実施例1と
同様にして水性フレキソインキを作成し、同様の評価を
行い、その結果を表2に示す。Comparative Example 1 Water-dispersible resin (a) 0.4 part Pigment (Carmine 6B) 16.0 parts Extender pigment (calcium carbonate) 5.0 parts Anionic activator 0.6 parts Water 24.9 parts The composition is made into a concentrated pigment aqueous solution with Red Tevir. Next, the following composition and the organometallic compound and epoxy compound shown in Table 1 were added to the obtained high-concentration dispersion aqueous solution to obtain an aqueous flexo ink. A water-based flexo ink was prepared in the same manner as in Example 1 and evaluated in the same manner, and the results are shown in Table 2.
【0021】比較例2 比較例1にて用いた水分散型樹脂(a)を水分散型樹脂
(c)にかえ、表1に示す有機金属化合物、エポキシ化
合物を添加し、それ以外は実施例1と同様にして水性フ
レキソインキを作成し、同様の評価を行い、その結果を
表2に示す。Comparative Example 2 The water-dispersible resin (a) used in Comparative Example 1 was replaced with the water-dispersible resin (c), and the organometallic compounds and epoxy compounds shown in Table 1 were added. A water-based flexo ink was prepared in the same manner as in Example 1 and evaluated in the same manner. The results are shown in Table 2.
【0022】[0022]
【発明の効果】本発明により、特にラミネート印刷構成
物を作成する時に1液型で安定で刷り易いインキであっ
て、ポリオレフィンフィルムのラミネート貼り合せ時の
接着強度の低下もなく、後加工で使用される芳香族系溶
剤、特にトルエンに対して、耐性の優れたインキ膜を提
供をすることができた。INDUSTRIAL APPLICABILITY According to the present invention, it is a one-pack type ink which is stable and easy to print, especially when a laminated printing composition is prepared, and does not lower the adhesive strength when laminating a polyolefin film and is used in post-processing. It was possible to provide an ink film having excellent resistance to the aromatic solvent used, particularly toluene.
【表1】 [Table 1]
【表2】 [Table 2]
Claims (1)
分散型樹脂を用い、該樹脂がカルボキシル基および/ま
たは水酸基を含有し、金属キレート化合物が1〜5重量
%、エポキシ化合物1〜10重量%含有することを特徴
とする水性フレキソインキ組成物。1. A water-soluble resin and a water-dispersible resin are used as main resin components, the resin contains a carboxyl group and / or a hydroxyl group, a metal chelate compound is 1 to 5% by weight, and an epoxy compound is 1 to 10% by weight. A water-based flexo ink composition comprising:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP35512791A JPH05171087A (en) | 1991-12-20 | 1991-12-20 | Water-base flexographic ink composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP35512791A JPH05171087A (en) | 1991-12-20 | 1991-12-20 | Water-base flexographic ink composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH05171087A true JPH05171087A (en) | 1993-07-09 |
Family
ID=18442102
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP35512791A Pending JPH05171087A (en) | 1991-12-20 | 1991-12-20 | Water-base flexographic ink composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH05171087A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009154281A1 (en) * | 2008-06-19 | 2009-12-23 | ダイナパック株式会社 | Printed material and method for producing printed material |
-
1991
- 1991-12-20 JP JP35512791A patent/JPH05171087A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009154281A1 (en) * | 2008-06-19 | 2009-12-23 | ダイナパック株式会社 | Printed material and method for producing printed material |
JP5243542B2 (en) * | 2008-06-19 | 2013-07-24 | ダイナパック株式会社 | Printed matter and printed matter manufacturing method |
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