JPS6336638B2 - - Google Patents
Info
- Publication number
- JPS6336638B2 JPS6336638B2 JP12367083A JP12367083A JPS6336638B2 JP S6336638 B2 JPS6336638 B2 JP S6336638B2 JP 12367083 A JP12367083 A JP 12367083A JP 12367083 A JP12367083 A JP 12367083A JP S6336638 B2 JPS6336638 B2 JP S6336638B2
- Authority
- JP
- Japan
- Prior art keywords
- ink
- formula
- printing
- organopolysiloxane
- lithographic printing
- 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
Landscapes
- Inks, Pencil-Leads, Or Crayons (AREA)
Description
本発明は、湿し水を用いる平版印刷用インキ組
成物に関する。
平版印刷版は油脂性のインキを受理する親油性
の画線部分とインキを受けつけない撥油性の非画
線部からなり、一般に非画線部は水を受けつける
親水性部分から構成される。従つて、通常の平版
印刷はインキと水の両方を版面に供給し、画線部
は着色性のインキを非画線部は水を選択的に受入
れ、画線上のインキを例えば紙などの基質に転写
されることによつてなされている。湿し水を使用
する平版印刷版としては、ジアゾニウム化合物を
用いたプレセンシタイズド版(いわゆるPS版)、
酸化亜鉛や有機光導電体を用いた電子写真方式に
よる平版印刷版、ハロゲン化銀乳剤を感光成分と
して用いた銀塩写真方式による平版印刷版などが
知られており、そのような平版印刷版での印刷に
使用されるインキにも多種多様なものが知られて
いる。しかし、これまでの印刷インキは、ある特
定の印刷版であるとか、湿し水であるとかの場合
には、良好な印刷物を得ることができても、それ
らの種類や印刷条件が変化することによつて種々
の欠点が生じ、場合によつては全く使用すること
ができないこともある。このような印刷インキに
要求される性質としては、画線部には十分量のイ
ンキが付着し、非画線部には全くインキが付着し
ないことが重要であることは言うまでもないこと
であるが、更に湿し水による乳化を起さずに上記
性質が得られなければならないことである。ま
た、前述したように、版材や湿し水の種類あるい
は印刷条件等が変わつても影響を受けないことが
望まれる。
本発明の目的は、上述した如き要求を満たす湿
し水使用の平版印刷用インキ組成物を提供するこ
とである。
本発明者等は、前記目的を達成するために鋭意
研究を重ねた結果、以下に述べるような化合物を
含むインキ組成物を用いることによつて、非画線
部に汚れを生じ難く、画線部には十分な濃度を与
え、乳化が起り難く、しかも条件変化に対する寛
容性の大きな湿し水使用の平版印刷が可能になる
ことを見出した。かかる化合物は、置換基Aおよ
び置換基Bの2種の置換基をそれぞれ少なくとも
1つ含有するオルガノポリシロキサンである。こ
こに置換基Aは式
(式中xは0〜4の整数を、aは平均1〜50の
数を、bは平均0〜50の数を、R′は水素原子、
アルキル基、アシル基を表わす)で示され、置換
基Bは式
The present invention relates to a lithographic printing ink composition using dampening water. A lithographic printing plate consists of an oleophilic image area that accepts oil-based ink and an oil-repellent non-image area that does not accept ink, and the non-image area generally consists of a hydrophilic area that accepts water. Therefore, in normal lithographic printing, both ink and water are supplied to the plate surface, the image area selectively receives colored ink and the non-image area selectively receives water, and the ink on the image area is transferred to a substrate such as paper. This is done by being transcribed into . Lithographic printing plates that use dampening water include presensitized plates (so-called PS plates) that use diazonium compounds,
Planographic printing plates based on an electrophotographic method using zinc oxide or an organic photoconductor, and planographic printing plates based on a silver salt photographic method using a silver halide emulsion as a photosensitive component are known. A wide variety of inks are known for use in printing. However, with conventional printing inks, even if good prints can be obtained in the case of a specific printing plate or dampening solution, the type and printing conditions may change. Depending on the situation, various drawbacks may occur, and in some cases, it may not be possible to use it at all. It goes without saying that the properties required of such printing ink are that a sufficient amount of ink adheres to the printed areas and that no ink adheres to non-printed areas. Furthermore, the above properties must be obtained without causing emulsification with dampening water. Further, as mentioned above, it is desirable that the printing method be unaffected even if the plate material, type of dampening solution, printing conditions, etc. change. An object of the present invention is to provide an ink composition for lithographic printing using dampening water that satisfies the above-mentioned requirements. As a result of extensive research to achieve the above object, the present inventors have found that by using an ink composition containing the compounds described below, stains are less likely to occur in non-image areas, and image lines are less likely to be stained. It has been found that it is possible to perform lithographic printing using dampening water by giving sufficient concentration to the parts, making emulsification less likely to occur, and having greater tolerance to changes in conditions. Such a compound is an organopolysiloxane containing at least one of each of two substituents, substituent A and substituent B. Here, substituent A has the formula (In the formula, x is an integer from 0 to 4, a is a number from 1 to 50 on average, b is a number from 0 to 50 on average, R' is a hydrogen atom,
represents an alkyl group or an acyl group), and the substituent B is represented by the formula
【式】又は[Formula] or
O―リン酸 10g
硝酸ニツケル 5g
亜硝酸ナトリウム 5g
エチレングリコール 100g
コロイダルシリカ(20%液) 23ml
水を加えて20とする
〔インキ(A)の処方および製造法〕
Γ 処方
印刷インキ用カーボンブラツク 200
フタロシアニンブルー 50
ロジン変性フエノール樹脂 200
シリコーン変性アルキド樹脂(a1) 200
亜麻仁油 100
高沸点溶剤(0号ソルベントH) 200
ワツクスコンパウンド 40ナフテン酸コバルト塩(金属濃度7.5%) 10
計 1000部
上記混合物を三本ロールを用いて均一に混練し
てインキ(A)を得た。
Γ シリコーン変性アルキド樹脂(a1)の製造
無水フタル酸 100部
オレフイン酸 50部
グリセリン 50部
上記例示化合物(3) 25部
イソホロン 25部
ブチルセロソルブ 200部
上記混合物を150℃で2時間反応させてシリコ
ーン変性アルキド樹脂(a1)を得た。
〔インキ(B)の処方および製造法〕
インキ(A)の例示化合物(3)の代りに下記の化合物
(b)を用いる以外は、インキ(A)と全く同様にして製
造した。
化合物 (b)
実施例 2
実施例1のインキ(A)において顔料としてジスア
ゾイエローカーミン6Bとフタロシアニンブルー
とを使用してもインキの製造は可能であり、有色
インキで地汚れが出易い前記平版印刷版でもそれ
ら欠点が全くない良好な印刷ができることが確認
された。
実施例 3
実施例1のインキ(A)に用いたアルキド樹脂と例
示化合物(3)とを予め常温で混練してインキ添加組
成物とし、インキ(A)のシリコーン変性アルキド樹
脂(a1)の代りに用いた。インキ(A)と同様の結果
が得られ、本発明のインキ組成物は必ずしも加熱
反応物である必要はないことが確認された。
実施例 4
シリコーン変性アルキド樹脂(a1)の製造に用
いた例示化合物(3)を例示化合物(1)、(2),(4)または
(5)に代える以外は全く同様にして実施例1を繰り
返したところ、インキ(A)と同じ結果が得られた。
シリコーン変性アルキド樹脂の製造法について
は、例えば特開昭50−71410、同50−71411号公報
等に詳述されているのでこれらを参照することが
できる。
実施例 5
下記のインキを用いて実施例1と同様に印刷し
たところ、実施例1のインキ(A)と同様な結果が得
られた。
印刷インキ用カーボンブラツク 200
フタロシアニンブルー 50
ロジン変性フエノール樹脂ワニス(a2) 400
ワツクスコンパウンド 40
ナフテン酸コバルト塩(金属濃度7.5%) 10
ナフテン酸マンガン塩(金属濃度6.5%) 10
0号ソルベントH(日本石油) 290
Γ 上記ロジン変性フエノール樹脂ワニス(a2)
の処方
ロジン変性アルキルフエノール樹脂 500
シリコーン変性亜麻仁油(a21) 300
脱水ひまし油 200
Γ 上記シリコーン変性亜麻仁油(a21)の製造
法
亜麻仁油 700例示化合物(3) 300
計 1000部
上記組成からなる混合物を150℃で3時間反応
させて本発明のインキ組成物とした。
例示化合物(2)に代えて他の例示化合物(1)及び(5)
を用いた場合にも同様の結果が得られた。
シリコーン変性植物油の製造法については例え
ば特開昭51−21906、同51−21907号公報等に詳述
されているのでこれらを参照されたい。
実施例 6
インキタツク値および色が異なる7種の市販イ
ンキ組成物に実施例1〜5で用いられた本発明の
インキ組成物を10重量%加えてよく混練したイン
キと未添加の市販インキとを用いて印刷したとこ
ろ、いずれも実施例1で得られた結果と同様の結
果が得られた。
実施例 7
市販のPS版および酸化亜鉛を用いた印刷版を
それぞれ専用の湿し水を用いて実施例6を繰り返
した。いずれの平版印刷版においても顕著な差が
認められた。
実施例 8
市販のインキ組成物に例示化合物(1)または(4)を
2重量%加えてよく混練したインキと未添加のイ
ンキとを用いて印刷したところ、実施例6と同様
の結果が得られた。
O-phosphoric acid 10g Nickel nitrate 5g Sodium nitrite 5g Ethylene glycol 100g Colloidal silica (20% liquid) 23ml Add water to make 20 [Ink (A) formulation and manufacturing method] Γ Carbon black for prescription printing ink 200 Phthalocyanine Blue 50 Rosin modified phenolic resin 200 Silicone modified alkyd resin (A 1 ) 200 Linseed oil 100 High boiling point solvent (No. 0 Solvent H) 200 Wax compound 40 Cobalt naphthenate salt (metal concentration 7.5%) 10 total 1000 parts of the above mixture Ink (A) was obtained by uniformly kneading the mixture using three rolls. Γ Production of silicone-modified alkyd resin (a 1 ) Phthalic anhydride 100 parts Olefiic acid 50 parts Glycerin 50 parts Exemplary compound (3) 25 parts Isophorone 25 parts Butyl cellosolve 200 parts The above mixture was reacted at 150°C for 2 hours to undergo silicone modification. An alkyd resin (a 1 ) was obtained. [Formulation and manufacturing method of ink (B)] The following compound in place of exemplified compound (3) in ink (A)
It was produced in exactly the same manner as ink (A) except that (b) was used. compound (b) Example 2 It is possible to produce an ink using disazo yellow carmine 6B and phthalocyanine blue as pigments in the ink (A) of Example 1, and the above-mentioned lithographic printing plate, which is prone to scumming with colored inks, also has these drawbacks. It was confirmed that good printing was possible with no blemishes at all. Example 3 The alkyd resin used in the ink (A) of Example 1 and the exemplified compound (3) were kneaded in advance at room temperature to prepare an ink additive composition, and the silicone-modified alkyd resin (a 1 ) of the ink (A) was kneaded in advance at room temperature. used instead. The same results as ink (A) were obtained, and it was confirmed that the ink composition of the present invention does not necessarily have to be a heat reactant. Example 4 Example compound (3) used in the production of silicone-modified alkyd resin (a 1 ) was converted into example compound (1), (2), (4) or
When Example 1 was repeated in exactly the same manner except for replacing ink (5), the same results as ink (A) were obtained.
The method for producing silicone-modified alkyd resins is described in detail in, for example, Japanese Patent Application Laid-open Nos. 50-71410 and 50-71411, which can be referred to. Example 5 When printing was carried out in the same manner as in Example 1 using the following ink, the same results as ink (A) of Example 1 were obtained. Carbon black for printing ink 200 Phthalocyanine blue 50 Rosin-modified phenolic resin varnish ( A2 ) 400 Wax compound 40 Cobalt naphthenate salt (metal concentration 7.5%) 10 Manganese naphthenate salt (metal concentration 6.5%) 10 No. 0 Solvent H ( Nippon Oil) 290 Γ Above rosin modified phenolic resin varnish (a 2 )
Prescription of rosin-modified alkylphenol resin 500 Silicone-modified linseed oil (A 21 ) 300 Dehydrated castor oil 200 Γ Manufacturing method of the above-mentioned silicone-modified linseed oil (A 21 ) Linseed oil 700 Exemplary compound (3) 300 Total 1000 parts Mixture consisting of the above composition were reacted at 150°C for 3 hours to obtain the ink composition of the present invention. Other exemplified compounds (1) and (5) in place of exemplified compound (2)
Similar results were obtained when using . The method for producing silicone-modified vegetable oil is described in detail in, for example, Japanese Patent Application Laid-open Nos. 51-21906 and 51-21907, so please refer to these. Example 6 10% by weight of the ink composition of the present invention used in Examples 1 to 5 was added to seven types of commercially available ink compositions with different ink tack values and colors, and the ink was well kneaded and the commercially available ink without additives was mixed. When printing was carried out using these materials, the same results as those obtained in Example 1 were obtained. Example 7 Example 6 was repeated using a commercially available PS plate and a printing plate using zinc oxide, each using their own dampening water. A remarkable difference was observed in all planographic printing plates. Example 8 When printing was carried out using an ink prepared by adding 2% by weight of exemplified compound (1) or (4) to a commercially available ink composition and well-kneaded, and an ink without the additive, the same results as in Example 6 were obtained. It was done.
Claims (1)
用インキ組成物であつて、該組成物が含有してい
る前記オルガノポリシロキサンは、1分子中に下
記式A及び式Bの2種の置換基をそれぞれ少なく
とも1つ含有することを特徴とする湿し水使用の
平版印刷用インキ組成物。 式A; (式中xは0〜4の整数を、aは平均1〜50の
数を、bは平均0〜50の数を、R′は水素原子、
アルキル基、アシル基を表わす。) 式B;【式】または 【式】 (式中yは0〜4の整数を、R″及びRは末
端不飽和結合を含まない炭素数1〜30の飽和また
は不飽和炭化水素を、zは2〜30の整数を表わ
す。) 2 当該オルガノポリシロキサンを、当該オルガ
ノポリシロキサンに対して混和性を有する樹脂も
しくは油との混和物ないしそれらとの反応物の形
で含有する特許請求の範囲第1項に記載の平版印
刷用インキ組成物。[Scope of Claims] 1. A lithographic printing ink composition containing an organopolysiloxane, wherein the organopolysiloxane contained in one molecule contains two types of the following formulas A and B. An ink composition for lithographic printing using dampening water, characterized in that it contains at least one substituent. Formula A; (In the formula, x is an integer from 0 to 4, a is a number from 1 to 50 on average, b is a number from 0 to 50 on average, R' is a hydrogen atom,
Represents an alkyl group or an acyl group. ) Formula B; [Formula] or [Formula] (In the formula, y is an integer of 0 to 4, R'' and R are saturated or unsaturated hydrocarbons having 1 to 30 carbon atoms that do not contain terminal unsaturated bonds, z represents an integer from 2 to 30.) 2. Claims containing the organopolysiloxane in the form of a mixture with or a reactant with a resin or oil that is miscible with the organopolysiloxane. The lithographic printing ink composition according to item 1.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58123670A JPS6015476A (en) | 1983-07-07 | 1983-07-07 | Printing ink composition and additive for ink |
| US06/540,170 US4589920A (en) | 1982-10-08 | 1983-10-07 | Ink composition utilized in lithographic printing and a lithographic printing process |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58123670A JPS6015476A (en) | 1983-07-07 | 1983-07-07 | Printing ink composition and additive for ink |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6015476A JPS6015476A (en) | 1985-01-26 |
| JPS6336638B2 true JPS6336638B2 (en) | 1988-07-21 |
Family
ID=14866387
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58123670A Granted JPS6015476A (en) | 1982-10-08 | 1983-07-07 | Printing ink composition and additive for ink |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6015476A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002194260A (en) * | 2000-12-22 | 2002-07-10 | Dainippon Ink & Chem Inc | Lithographic printing ink composition |
-
1983
- 1983-07-07 JP JP58123670A patent/JPS6015476A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6015476A (en) | 1985-01-26 |
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