JPS645825B2 - - Google Patents
Info
- Publication number
- JPS645825B2 JPS645825B2 JP59084139A JP8413984A JPS645825B2 JP S645825 B2 JPS645825 B2 JP S645825B2 JP 59084139 A JP59084139 A JP 59084139A JP 8413984 A JP8413984 A JP 8413984A JP S645825 B2 JPS645825 B2 JP S645825B2
- Authority
- JP
- Japan
- Prior art keywords
- ink
- printing
- paper
- wet paper
- resin
- 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
Links
- 239000011347 resin Substances 0.000 claims description 32
- 229920005989 resin Polymers 0.000 claims description 32
- 238000007639 printing Methods 0.000 claims description 29
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 19
- 239000002904 solvent Substances 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- 239000003086 colorant Substances 0.000 claims description 11
- 239000000835 fiber Substances 0.000 claims description 5
- 239000000463 material Substances 0.000 claims description 4
- 238000009835 boiling Methods 0.000 claims description 3
- 238000007644 letterpress printing Methods 0.000 claims description 3
- 239000013043 chemical agent Substances 0.000 claims 1
- 239000000976 ink Substances 0.000 description 55
- 238000001035 drying Methods 0.000 description 14
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 13
- 239000003981 vehicle Substances 0.000 description 11
- 239000000126 substance Substances 0.000 description 9
- 239000000654 additive Substances 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 239000000049 pigment Substances 0.000 description 6
- 150000002334 glycols Chemical class 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 239000006229 carbon black Substances 0.000 description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 4
- 150000002689 maleic acids Chemical class 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 235000011941 Tilia x europaea Nutrition 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000004571 lime Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 2
- 230000001376 precipitating effect Effects 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 2
- 239000003021 water soluble solvent Substances 0.000 description 2
- DTCCVIYSGXONHU-CJHDCQNGSA-N (z)-2-(2-phenylethenyl)but-2-enedioic acid Chemical compound OC(=O)\C=C(C(O)=O)\C=CC1=CC=CC=C1 DTCCVIYSGXONHU-CJHDCQNGSA-N 0.000 description 1
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 1
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
- COBPKKZHLDDMTB-UHFFFAOYSA-N 2-[2-(2-butoxyethoxy)ethoxy]ethanol Chemical compound CCCCOCCOCCOCCO COBPKKZHLDDMTB-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000557626 Corvus corax Species 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 239000001293 FEMA 3089 Substances 0.000 description 1
- 239000004705 High-molecular-weight polyethylene Substances 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000007824 aliphatic compounds Chemical class 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000013016 damping Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- -1 glycol ethers Chemical class 0.000 description 1
- 238000007646 gravure printing Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000004898 kneading Methods 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
- 239000002184 metal Substances 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- 239000003799 water insoluble solvent Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M1/00—Inking and printing with a printer's forme
- B41M1/26—Printing on other surfaces than ordinary paper
Landscapes
- Printing Methods (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Description
【発明の詳細な説明】
本発明は、抄造工程の紙層形成直後の多量の水
分を含む湿紙に鮮明に図形印刷する湿紙印刷方法
に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a wet paper paper printing method for clearly printing figures on wet paper paper containing a large amount of water immediately after forming a paper layer in a papermaking process.
証券用紙のように定位置すき入れの長巻紙に
は、枚葉紙に自動断裁するときの断裁位置を示す
マークが必要である。このマークは、乾燥部での
用紙伸縮の影響を避けるため、抄造工程中の湿紙
の状態で作成する必要がある。従前は直径約2mm
のレジスターホールを抄造の途中で入れていた
が、断裁精度をより一層向上するため、ホールよ
りも更に形の鮮明なマークを、抄造工程で湿紙の
すき入模様に対する一定位置に凸版方式で印刷す
る方法を発明したものである。 Long-roll paper that is punched in a fixed position, such as securities paper, requires a mark to indicate the cutting position when automatically cutting sheets. This mark must be created while the wet paper is in the papermaking process to avoid the effects of paper expansion and contraction in the drying section. Previously, the diameter was approximately 2mm
Register holes were previously inserted in the middle of the papermaking process, but in order to further improve cutting accuracy, a mark with a clearer shape than the holes was printed using a letterpress method at a fixed position relative to the perforated pattern on the wet paper during the papermaking process. We invented a method to do this.
湿紙に印刷することはこれまでに実施例がな
く、この場合、これを阻害する最も困難な問題は
紙むけの発生であつた。即ち、紙層は形成されて
いるが、繊維結合がまだ十分でない湿紙に版面上
のインキが接触すると、湿紙の繊維はインキの粘
性で版面上にむしり取られ、湿紙へのインキ付着
よりも紙の繊維が版面側に粘着する方が多くな
る。この傾向はインキの粘度をかなり低くしても
印刷が進むにつれて増大するので、従来の凸版、
平版、凹版印刷に用いられているようなインキは
使用できない。また、グラビア印刷用の蒸発乾燥
型インキのように低粘度のものでも、版面から紙
に接触した時に蒸発や浸透が始まり、結果的に粘
度が上昇し紙むけが発生する。従つて、この問題
一つ取り上げてみてもインキ組成上かなりの工夫
を要することが分る。 There has been no practical example of printing on wet paper, and in this case, the most difficult problem that hindered this was the occurrence of paper peeling. In other words, when the ink on the printing plate comes into contact with a wet paper that has formed a paper layer but has not yet had sufficient fiber bonding, the fibers of the wet paper are stripped onto the printing plate by the viscosity of the ink, causing the ink to adhere to the wet paper. Also, the paper fibers tend to stick to the plate side. This tendency increases as printing progresses even if the ink viscosity is considerably lowered, so conventional letterpress printing
Inks such as those used in lithographic and intaglio printing cannot be used. Furthermore, even low-viscosity inks such as evaporative inks for gravure printing begin to evaporate and permeate when they come into contact with paper from the printing plate, resulting in increased viscosity and paper peeling. Therefore, even if we take up this problem alone, we can see that considerable ingenuity is required in terms of ink composition.
次に第2の問題はインキの転移性で、かなりの
量の水分と繊維とから構成されている湿紙層は乾
いた紙と異なり、インキの吸収性が劣るためその
表面にインキ被膜を均一に載せることは極めて難
しい。 The second problem is the transferability of the ink. Unlike dry paper, the wet paper layer, which is composed of a considerable amount of water and fibers, has poor ink absorption properties, so it forms an even ink film on its surface. It is extremely difficult to put it on.
更に第3の問題はインキの乾燥である印刷後の
湿紙が乾燥部に入るまでの短時間内にインキが乾
燥し、且つ又、インキ乾燥皮膜が耐熱性を有しな
いと毛布や乾燥筒の表面にインキが付着し、後続
の紙を汚染する。 Furthermore, the third problem is ink drying.If the ink dries within a short time before the wet paper enters the drying section after printing, and if the ink drying film does not have heat resistance, the blanket or drying tube will not dry. Ink adheres to the surface and contaminates subsequent paper.
既知の各種インキを湿紙印刷に試用した結果は
次のとおりであり、いずれも実用できなかつた。 The results of trials using various known inks for wet paper printing are as follows, and none of them could be put to practical use.
油性ビヒクルを使用する一般の酸化重合乾燥型
のインキは、その粘性のために紙むけが発生し、
又、水と油の反発により湿紙へインキが転移しに
くく、乾燥も遅すぎるので全く適さない。 Typical oxidative polymerization drying inks that use oil-based vehicles tend to peel due to their viscosity.
In addition, ink is difficult to transfer to wet paper due to the repulsion of water and oil, and drying is too slow, making it completely unsuitable.
事務用の浸透乾燥型(スタンプ用や万年筆用)
インキは乾燥が極端に遅く、耐熱性も不良で適さ
ない。 Penetration drying type for office use (for stamps and fountain pens)
Ink is extremely slow to dry and has poor heat resistance, making it unsuitable.
低沸点溶剤と樹脂及び着色剤を組合せた蒸発乾
燥型インキは湿紙上に転移するが、市販の油性及
び水性フエルトペン用インキではこの目的に対し
ては乾燥が遅く耐熱性にも欠ける。更に低沸点の
溶剤であるアセトン、ベンゼン、エチルアルコー
ル等を溶剤とする蒸発乾燥型インキは乾燥が早く
なるが、それに伴つて紙むけを起こしやすく、
又、揮発性が強すぎてインキに安定性がなく印刷
は困難であつた。 Evaporative inks that combine low-boiling solvents with resins and colorants transfer onto wet paper, but commercially available oil-based and water-based felt pen inks dry slowly and lack heat resistance for this purpose. Furthermore, evaporative drying inks that use low-boiling point solvents such as acetone, benzene, and ethyl alcohol dry quickly, but are also prone to paper peeling.
In addition, the ink was too volatile and unstable, making printing difficult.
スチームセツトインキは段ボール印刷等に用い
られ、ビヒクルとして一般に水と相溶性のジエチ
レングリコールのようなグリコール類に、水に不
溶の高酸化のロジン変性マレイン酸樹脂を溶解し
たものを用い、印刷後に水蒸気を印刷物に吹きつ
けて水と相溶性の溶剤を水分で希釈し、樹脂分を
析出させることにより短時間でインキを乾燥させ
るものである。この方法による湿紙の印刷では、
印刷後に水蒸気を吹きつけるまでもなく、印刷と
同時に溶剤分が水に拡散し、水に不溶の樹脂分が
用紙上に析出しインキが乾燥する傾向が認められ
た。しかし、インキが紙に接触した瞬間から乾燥
が始まるため、紙むけ傾向は試用したインキの中
では最も激しく、インキ転移性も不十分でそのま
までは実用できなかつた。 Steam set ink is used for printing on corrugated boards, etc., and is generally made by dissolving water-insoluble highly oxidized rosin-modified maleic acid resin in a water-compatible glycol such as diethylene glycol as a vehicle, and then releasing water vapor after printing. This method dries the ink in a short time by spraying it on the printed material to dilute the water-compatible solvent with water and precipitating the resin component. In wet paper printing using this method,
There was a tendency for the solvent to diffuse into the water at the same time as printing without spraying water vapor after printing, and for water-insoluble resin to precipitate on the paper, causing the ink to dry. However, because the ink begins to dry the moment it comes into contact with paper, it had the most severe paper peeling tendency of all the inks tested, and its ink transfer properties were insufficient, making it unsuitable for practical use as it was.
そこでこの発明においては、インキ成分とし
て、乾燥機構が湿紙印刷に比較的適していたグリ
コール系溶剤と樹脂を組合せたビヒクルを用い、
紙むけ防止の一助として溶剤量を一般インキより
も著しく多い70〜95%にしてインキ粘度を極端に
下げた。更にインキを湿紙上に均一に転移させる
ための工夫として湿紙中へのインキ浸透性を促進
するように、溶剤としてジエチレングリコールを
始めとする表面張力の大きいグリコール類の使用
をやめ、表面張力の小さいグリコールエーテルを
主に用いることとした。ただし、インキの乾燥速
度調整などのためにグリコールを一部混合使用す
ることは一向に差しつかえない。又、水との接触
によつて樹脂が析出することを妨げない範囲で他
の水溶性溶剤更には水に不溶性の溶剤の一部添加
も可能である。 Therefore, in this invention, a vehicle that combines a glycol solvent and a resin, whose drying mechanism is relatively suitable for wet paper printing, is used as an ink component.
To help prevent paper peeling, the ink viscosity was extremely reduced by using 70 to 95% solvent, which is significantly higher than in general inks. Furthermore, in order to uniformly transfer the ink onto the wet paper, we stopped using diethylene glycol and other glycols with a high surface tension as solvents, and instead used glycols with a low surface tension to promote ink penetration into the wet paper. We decided to mainly use glycol ether. However, there is absolutely no problem in mixing and using a portion of glycol for purposes such as adjusting the drying speed of the ink. Further, it is also possible to add other water-soluble solvents or a portion of water-insoluble solvents within a range that does not prevent the resin from precipitating on contact with water.
主たる溶剤のグリコールエーテルとしては、沸
点が170℃以上の例えばブチルセロソルブやメチ
ル−、エチル−、プロピル−、ブチル−カルビト
ール、更にはメチル−、エチル−、プロピル−、
ブチル−、トリグリコールが使用可能である。
又、グリコール類としては、エチレングリコール
から高分子量ポリエチレングリコールまでの分子
量の異なるエチレングリコールやプロピレングリ
コールのいずれもがグリコールエーテルと混合使
用可能である。その他グリコール類のモノ脂肪酸
エステルのような水溶性溶剤やグリコール類のモ
ノ又はジのエーテル、エステルあるいは脂肪族、
芳香族系の水に一部可溶あるいは水に不溶性の溶
剤も一部であれば混合使用できる。 Examples of the main solvent glycol ether include butyl cellosolve, methyl, ethyl, propyl, butyl carbitol, and methyl, ethyl, propyl,
Butyl and triglycols can be used.
Further, as glycols, any of ethylene glycol and propylene glycol having different molecular weights from ethylene glycol to high molecular weight polyethylene glycol can be used in combination with glycol ether. Other water-soluble solvents such as mono-fatty acid esters of glycols, mono- or di-ethers, esters or aliphatic compounds of glycols,
Aromatic solvents that are partially soluble in water or insoluble in water can also be mixed and used.
樹脂は前記のグリコールエーテル類の単独又は
混合溶剤に可溶のものを用いるが、あまり溶け易
いとインキが水に接触した際の樹脂の析出速度が
遅く、インキの乾燥速度が不十分となるので、使
用する溶剤に対応して樹脂を選択する必要があ
る。本目的に適した樹脂としてはロジン変性フエ
ノール樹脂(例えば荒川化学工業製タマノール
350)、アルキルフエノール樹脂(日立化成製ヒタ
ノール1133)、キシレン樹脂、クマロン樹脂、エ
ステルレジン(荒川化学工業製ペンセル〓、ペン
セルA)、エチルセルロース、硬化ロジン(荒川
化学工業製ライムレジンNo.3、ライムレジンNo.
23C)、スチレン−マイレン酸共重合樹脂(日本
触媒化学製オキシラツクSH−101)、アクリル樹
脂(星光化学工業製ハイロスAW−36)、酢酸酪
酸セルロース、ブチラール樹脂(積水化学製エス
レツクBL−1、エスレツクBL−2)、酸価が200
以下のロジン変性マレイン酸樹脂(荒川化学工業
製マルキード樹脂)などがある。スチームセツト
インキに一般的に用いられる高酸価(約300)の
ロジン変性マレイン酸樹脂(荒川化学工業製マル
キードNo.33)も、溶剤にジエチレングリコールを
多目に混合使用した場合には乾燥速度も大きく有
効であつた。 The resin to be used is one that is soluble in the aforementioned glycol ethers alone or in a mixed solvent; however, if the resin is too soluble, the precipitation rate of the resin will be slow when the ink comes into contact with water, and the drying rate of the ink will be insufficient. , it is necessary to select the resin according to the solvent used. Resins suitable for this purpose include rosin-modified phenolic resins (for example, Tamanol manufactured by Arakawa Chemical Industries)
350), alkylphenol resin (Hitanol 1133 manufactured by Hitachi Chemical Co., Ltd.), xylene resin, coumaron resin, ester resin (Pensel®, Pencell A manufactured by Arakawa Chemical Co., Ltd.), ethyl cellulose, hardened rosin (Lime Resin No. 3, manufactured by Arakawa Chemical Co., Ltd., Lime) Resin No.
23C), styrene-maleic acid copolymer resin (Oxilac SH-101 manufactured by Nippon Shokubai Chemical Co., Ltd.), acrylic resin (Hyros AW-36 manufactured by Seiko Chemical Industry Co., Ltd.), cellulose acetate butyrate, butyral resin (Esslec BL-1 manufactured by Sekisui Chemical Co., Ltd., Esslec) BL-2), acid value is 200
Examples include the following rosin-modified maleic acid resin (Marquid resin manufactured by Arakawa Chemical Industries). Rosin-modified maleic acid resin (Marquid No. 33, manufactured by Arakawa Chemical Industries), which has a high acid value (approximately 300) and is commonly used in steam set inks, also has a slow drying rate when a large amount of diethylene glycol is mixed in the solvent. It was very effective.
本発明に欠くことができない要件として添加剤
の使用が挙げられる。添加剤は少量ではあるが各
種の効果に寄与している。すなわち、ビヒクル中
の樹脂同志あるいは樹脂と溶剤との結合力が強化
されて、水分混入によるインキのエマルシヨン化
を防止して、印刷中のインキ増粘を抑制し紙むけ
を減少させる。又、インキの均一な転移、インキ
皮膜の強化、乾燥促進にも効果を発揮する。添加
剤として有効な材料としてはオレイン酸、脱水ヒ
マシ油、脂肪酸、2−エチルヘキシルアルコー
ル、ヒマシ油、テレピン油、ジブチルフタレー
ト、ジオクチルフタレート、トリ−n−ブチルホ
スフエート、低分子量ヒドロキシプロピルセルロ
ース等が挙げられる。 An essential requirement of the present invention is the use of additives. Additives contribute to various effects, albeit in small amounts. That is, the bonding force between the resins in the vehicle or between the resin and the solvent is strengthened, preventing the ink from becoming an emulsion due to moisture contamination, suppressing ink thickening during printing, and reducing paper peeling. It is also effective in uniformly transferring ink, strengthening the ink film, and accelerating drying. Materials useful as additives include oleic acid, dehydrated castor oil, fatty acids, 2-ethylhexyl alcohol, castor oil, turpentine oil, dibutyl phthalate, dioctyl phthalate, tri-n-butyl phosphate, and low molecular weight hydroxypropyl cellulose. It will be done.
着色剤は主にラーベン1035(カーボンブラツク)
を用いたが、紙むけ防止を重点対策とした該イン
キでは、ビヒクルをかなり増量したので顔料濃度
を低く抑えざるを得なかつた。当然のことなが
ら、必要に応じて他の色彩の顔料や染料を使用す
ることは何ら差し支えない。 The coloring agent is mainly Raven 1035 (carbon black).
However, in this ink, which focused on preventing paper peeling, the amount of vehicle was increased considerably, so the pigment concentration had to be kept low. Naturally, pigments and dyes of other colors may be used as required.
使用するインキの粘度が低いため、これを均一
に版面に付着せしめるよう印刷機構の検討を行つ
た。すなわち、湿紙への印刷効果を高めるために
凸版の金属版面へのインキ着けローラ表面を、液
状物を吸収保持する機能のあるダンピングスリー
ブ(3M社製)等の保液性材料で被覆した。これ
により版面へのインキ着け量が一定となり、印刷
された図形にむらがなく着色濃度も向上した。 Since the viscosity of the ink used is low, we investigated the printing mechanism to ensure that it adheres uniformly to the plate surface. That is, in order to enhance the printing effect on wet paper, the surface of the ink application roller on the metal plate surface of the letterpress was coated with a liquid-retaining material such as a damping sleeve (manufactured by 3M) that has the function of absorbing and retaining liquid substances. As a result, the amount of ink applied to the printing plate was constant, resulting in uniform printed figures and improved color density.
以上の方法により湿紙上に断栽マーク用の図形
を鮮明に印刷することができた。 By the method described above, it was possible to clearly print the figure for the tree cutting mark on the wet paper.
以下、実施例により湿紙印刷用インキの組成に
ついて更に具体的に説明する。 Hereinafter, the composition of the wet paper printing ink will be explained in more detail with reference to Examples.
(各実施例中の部数は重量部である。)
実施例 1
溶 剤 ブチルトリグリコール 70部
樹 脂 硬化ロジン(荒川化学工業製ライムレ
ジンNo.3) 20部
添加剤 ジオクチルフタレート 3部
着色剤 カーボンブラツク(コロンビアカーボ
ン製ラーベン1035) 7部
練合作業は、まず上記成分の溶剤と樹脂を1:
1に配合し、200℃まで加熱、樹脂を溶解し、粘
度が約20ポイズ(30℃)のビヒクルを得る。次に
このビヒクルと着色剤の黒顔料を3本ロールミル
で顔料濃度20%として練合し、これを元インキと
して組成構成上で不足のビヒクル、溶剤、添加剤
を加えて高速撹拌機で均一に混合して実用インキ
とした。(The parts in each example are parts by weight.) Example 1 Solvent Butyl triglycol 70 parts Resin Cured rosin (Arakawa Chemical Co., Ltd. Lime Resin No. 3) 20 parts Additive Dioctyl phthalate 3 parts Colorant Carbon Black (Raben 1035 manufactured by Columbia Carbon) 7 parts For the kneading process, first mix the above components of solvent and resin in 1 part.
1 and heated to 200°C to dissolve the resin and obtain a vehicle with a viscosity of approximately 20 poise (30°C). Next, this vehicle and the black pigment as a colorant are kneaded in a three-roll mill to a pigment concentration of 20%, and this is used as the base ink, adding the vehicle, solvent, and additives that are insufficient in the composition, and uniformly using a high-speed stirrer. They were mixed to make a practical ink.
このインキ組成物を用いて、湿紙上に凸版印刷
方式により断栽マークを極めて鮮明に印刷するこ
とができた。 Using this ink composition, a tree cutting mark could be printed extremely clearly on wet paper by letterpress printing.
実施例 2
溶 剤 メチルトリグリコール 92部
樹 脂 ブチラール樹脂(積水化学製エスレツ
クBL−2) 5部
添加剤 2−エチルヘキシルアルコール 2部
着色剤 油性染料(オリエント化学製オイルブ
ルー#630) 1部
上記成分の着色剤以外を配合し、120℃まで加
熱、溶解し、80℃まで冷却後着色剤を添加、撹
拌、溶解して実用インキとした。Example 2 Solvent Methyl triglycol 92 parts Resin Butyral resin (Sekisui Chemical's Eslec BL-2) 5 parts Additive 2-ethylhexyl alcohol 2 parts Colorant Oil dye (Orient Chemical Oil Blue #630) 1 part Above components A practical ink was prepared by mixing ingredients other than the coloring agent, heating to 120°C, melting, and cooling to 80°C, adding the coloring agent, stirring, and dissolving.
このインキ組成物を用いて、実施例1と同様な
印刷を行うことができた。 Using this ink composition, printing similar to that in Example 1 could be performed.
実施例 3
溶 剤 メチルトリグリコール 42部
ジエチレングリコール 42部
樹 脂 ロジン変性マレイン酸樹脂(荒川化学
工業製マルキードNo.33) 10部
添加剤 オレイン酸 1部
着色剤 カーボンブラツク(三菱化成工業製カ
ーボンブラツクMA−100) 5部
上記成分のジエチレングリコールと樹脂を1:
1に配合し、200℃まで加熱、樹脂を溶解し、粘
度が約40ポイズ(30℃)のビヒクルを得る。この
ビヒクルと着色剤の黒顔料を3本ロールミルで顔
料濃度20%として練合し、これを元インキとして
組成上不足のビヒクル、溶剤、添加剤を加えて高
速撹拌機で均一に混合して実用インキとした。Example 3 Solvent Methyl triglycol 42 parts Diethylene glycol 42 parts Resin Rosin-modified maleic acid resin (Marquid No. 33 manufactured by Arakawa Chemical Industries) 10 parts Additive Oleic acid 1 part Colorant Carbon black (Carbon Black MA manufactured by Mitsubishi Chemical Industries, Ltd.) -100) 5 parts Diethylene glycol and resin of the above components 1 part
1 and heated to 200°C to dissolve the resin and obtain a vehicle with a viscosity of approximately 40 poise (30°C). This vehicle and black pigment as a coloring agent are kneaded in a three-roll mill to a pigment concentration of 20%, and this is used as a base ink, adding the vehicle, solvent, and additives that are insufficient in the composition, and mixing uniformly with a high-speed stirrer for practical use. Ink.
このインキ組成物を用いて、実施例1と同様な
印刷を行うことができた。 Using this ink composition, printing similar to that in Example 1 could be performed.
Claims (1)
に紙層を形成する繊維がまだ十分に結合していな
い状態の水分60〜75%を含む湿紙に、沸点が170
℃以上のグリコールエーテルを主体とする水と相
溶性の溶剤70〜95%、この溶剤に溶解し水に不溶
の樹脂3〜25%、着色剤0.5〜10%、紙むけ防止
を目的とする添加剤0.5〜5%を成分として含む
インキを用いて図形を印刷することを特徴とする
湿紙印刷方法。 2 前記の印刷において、保液性材料で表面を被
覆したインキ着けローラを印刷機構上に保有し
て、前記のインキを均一に版面まで転移せしめ凸
版印刷を行うことを特徴とする特許請求の範囲第
1項記載の湿紙印刷方法。[Claims] 1. Wet paper containing 60 to 75% moisture, where the fibers forming the paper layer are not yet fully bonded, such as wet paper immediately after press rolls on a paper machine, has a boiling point of 170%.
70-95% water-compatible solvent mainly consisting of glycol ether at temperature above ℃, 3-25% resin soluble in this solvent but insoluble in water, 0.5-10% coloring agent, addition for the purpose of preventing paper peeling. A wet paper printing method characterized by printing figures using ink containing 0.5 to 5% of a chemical agent as a component. 2. In the above-mentioned printing, an ink application roller whose surface is coated with a liquid-retaining material is held on the printing mechanism to uniformly transfer the ink to the plate surface to perform letterpress printing. The wet paper printing method according to item 1.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59084139A JPS60229785A (en) | 1984-04-27 | 1984-04-27 | Wet paper printing |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59084139A JPS60229785A (en) | 1984-04-27 | 1984-04-27 | Wet paper printing |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60229785A JPS60229785A (en) | 1985-11-15 |
| JPS645825B2 true JPS645825B2 (en) | 1989-02-01 |
Family
ID=13822158
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59084139A Granted JPS60229785A (en) | 1984-04-27 | 1984-04-27 | Wet paper printing |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60229785A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0791500B2 (en) * | 1991-10-25 | 1995-10-04 | 太田インキ製造株式会社 | Printing ink composition |
| JP2005048075A (en) * | 2003-07-29 | 2005-02-24 | Makii Engineering Kk | Quick-drying ink composition and printing method |
| JP2006321866A (en) * | 2005-05-18 | 2006-11-30 | Fuji Print Kogyo Kk | Ink for solvent shock process of producing electronic circuit substrate plate |
-
1984
- 1984-04-27 JP JP59084139A patent/JPS60229785A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60229785A (en) | 1985-11-15 |
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