JPS5952079B2 - Processing liquid for lithographic printing plates - Google Patents
Processing liquid for lithographic printing platesInfo
- Publication number
- JPS5952079B2 JPS5952079B2 JP12266276A JP12266276A JPS5952079B2 JP S5952079 B2 JPS5952079 B2 JP S5952079B2 JP 12266276 A JP12266276 A JP 12266276A JP 12266276 A JP12266276 A JP 12266276A JP S5952079 B2 JPS5952079 B2 JP S5952079B2
- Authority
- JP
- Japan
- Prior art keywords
- lithographic printing
- processing liquid
- copolymer
- printing plates
- solution
- 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
- Printing Plates And Materials Therefor (AREA)
Description
【発明の詳細な説明】
本発明は表面層が酸化亜鉛〜樹脂分散系の平版印刷版に
用いられる処理液に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a processing liquid used for a lithographic printing plate whose surface layer has a zinc oxide-resin dispersion system.
光導電性酸化亜鉛をシリコン樹脂、アクリル樹脂等の絶
縁性樹脂中に分散せしめた光導電層を有する電子写真感
光材料を常法により画像形成後、非画像部を不感脂化処
理して平版印刷版用マスターとして使用することが知ら
れている。After forming an image on an electrophotographic material having a photoconductive layer in which photoconductive zinc oxide is dispersed in an insulating resin such as silicone resin or acrylic resin by a conventional method, non-image areas are desensitized and lithographic printing is performed. It is known to be used as a plate master.
このような処理に使用される不感脂化液は多くの場合、
フェロシアン化物又はこれと水溶性リン酸塩を主成分と
するものである。そしてこの不感脂化液中でフェロシア
ン化物は解離すると、Fe(CN)O”−とFe(CN
)O゜−の各イオン間の平衡を生ずる。このような状態
の不感脂化液が酸化亜鉛の露出した非画像部に接すると
、この露出酸化亜鉛と反応して非画像部を不感脂化する
。しかし従来の不感脂化液においては特に光によるフェ
ロシアン化物の劣化が著し<、このため変質、沈澱等の
液の品質低下のみならず、平版印刷版の非画像部にいわ
ゆるギヤー目汚れや地汚れを発生させる原因を作つてい
た。本発明は以上の欠点を除去し、液の品質低下がなく
、ギヤー目汚れや地汚れを生じない平版印刷版用処理液
を提供するものである。Desensitizing liquids used in such treatments are often
The main components are ferrocyanide or ferrocyanide and water-soluble phosphate. When ferrocyanide dissociates in this desensitizing solution, it becomes Fe(CN)O”- and Fe(CN)
) creates an equilibrium between each ion of O°-. When the desensitizing liquid in such a state comes into contact with the exposed non-image area of zinc oxide, it reacts with the exposed zinc oxide and desensitizes the non-image area. However, in conventional desensitizing liquids, the deterioration of ferrocyanide, especially due to light, is remarkable.This not only deteriorates the quality of the liquid, such as deterioration and precipitation, but also causes so-called gear stains in the non-image areas of the lithographic printing plate. This was causing soiling. The present invention eliminates the above-mentioned drawbacks, and provides a processing liquid for lithographic printing plates that does not cause deterioration in the quality of the liquid and does not cause gear stains or background stains.
即ち本発明の処理液は塩基性重合性モノマーと重合性カ
ルボン酸金属塩とからなる親水性共重合体を有効成分と
して含有するものである。That is, the treatment liquid of the present invention contains a hydrophilic copolymer composed of a basic polymerizable monomer and a polymerizable carboxylic acid metal salt as an active ingredient.
このような親水性共重合体の具体例としてはアクリルア
ミド、ビニルピリジン、N−N’−ジメチルアミノエチ
ルメタクリレート、N−メチロールアクリルアミド、ア
クリルモルホリン、ビニルヒドロオキサム等の塩基性重
合性モノマーとアクリル酸マンガン、ビニル安息香酸コ
バルト、クロトン酸亜鉛、イタコン酸ニッケル、メタク
リル酸コバルト、メタクリル酸亜鉛等の重合性カルボン
酸金属塩との共重合体、更に具体的にはアクリルアミド
〜アクリル酸マンガン共重合体、ビニルピリジン〜ビニ
ル安息香酸コバルト共重合体、N・N’−ジメチルアミ
ノエチルメタクリレート〜クロトン酸亜鉛共重合体、N
−メチロールアクリルアミド〜イタコン酸ニッケル共重
合体、アクリルモルホリン〜メタクリル酸コバルト共重
合体、ビニルヒドロオキサム〜メタクリル酸ニッケル共
重合体等が挙げられる。Specific examples of such hydrophilic copolymers include basic polymerizable monomers such as acrylamide, vinylpyridine, N-N'-dimethylaminoethyl methacrylate, N-methylolacrylamide, acrylmorpholine, and vinylhydroxam, and acrylic acid. Copolymers with polymerizable carboxylic acid metal salts such as manganese, cobalt vinylbenzoate, zinc crotonate, nickel itaconate, cobalt methacrylate, zinc methacrylate, more specifically acrylamide-manganese acrylate copolymers, Vinyl pyridine - cobalt vinyl benzoate copolymer, N/N'-dimethylaminoethyl methacrylate - zinc crotonate copolymer, N
- Methyloacrylamide - nickel itaconate copolymer, acrylic morpholine - cobalt methacrylate copolymer, vinylhydroxam - nickel methacrylate copolymer and the like.
これらの親水性共重合体を作るには塩基性重合性モノマ
ー、重合性カルボン酸、重合開始剤及び水を反応容器に
入れて攪拌させながら反応せしめ、この反応物に酢酸金
属塩水溶液を混合し、70〜80℃に加熱反応させれば
よい。To make these hydrophilic copolymers, a basic polymerizable monomer, a polymerizable carboxylic acid, a polymerization initiator, and water are placed in a reaction vessel and reacted with stirring, and an aqueous metal acetate solution is mixed with the reactant. , the reaction may be carried out by heating at 70 to 80°C.
その製造例を以下に示す。製造例
アクリルアミド 70g
アクリル酸 213g
過硫酸カリ 4g
水 2657g
以上を混合し反応温度70〜80℃で6時間反応させる
。A manufacturing example thereof is shown below. Production Example Acrylamide 70g Acrylic acid 213g Potassium persulfate 4g Water 2657g The above ingredients were mixed and reacted at a reaction temperature of 70 to 80°C for 6 hours.
次に得られた親水性共重合体ポリマー1000gを酢酸
マンガン1%溶液500gと混合して反応温度80〜9
0℃で8時間反応させ、アクリルアミド〜アクリル酸マ
ンガンよりなる親水性共重合体金属塩を得る。Next, 1000 g of the obtained hydrophilic copolymer was mixed with 500 g of a 1% manganese acetate solution at a reaction temperature of 80 to 9.
The reaction is carried out at 0° C. for 8 hours to obtain a hydrophilic copolymer metal salt consisting of acrylamide and manganese acrylate.
こうして得られる親水性共重合体は通常0.1〜5重量
%の濃度で使用され、その親水性皮膜によつて非画像部
を容易に不感脂化することができる。The hydrophilic copolymer thus obtained is usually used at a concentration of 0.1 to 5% by weight, and the hydrophilic coating can easily desensitize non-image areas.
本発明の処理液にはその他、一般の不感脂化液に使用さ
れている各種添加剤、例えばリン酸アンモニウム、リン
酸ソーダ、リン酸等のPH緩衝剤;クエン酸、マロン酸
、乳酸、酒石酸、アミノ酸、各種無機酸又はそれらの塩
等のPH調節剤;グリセリン、グリコール、CMC、ビ
ニルピロリドン等の湿潤剤を添加することができる。In addition, the processing solution of the present invention includes various additives used in general desensitizing solutions, such as PH buffers such as ammonium phosphate, sodium phosphate, and phosphoric acid; citric acid, malonic acid, lactic acid, and tartaric acid. , amino acids, various inorganic acids, or salts thereof; wetting agents such as glycerin, glycol, CMC, vinylpyrrolidone, etc. can be added.
本発明の処理液は不感脂化処理後の平版印刷版にインキ
ングを行なう前に適用する湿し水としても使用できる。The treatment liquid of the present invention can also be used as a dampening solution to be applied before inking a lithographic printing plate after desensitization treatment.
この場合は処理液を6〜7倍程度に希釈して使用する。
以下に実施例及び比較例を示す。In this case, the treatment liquid is diluted approximately 6 to 7 times before use.
Examples and comparative examples are shown below.
実施例 1
アクリルアミド/アクリル酸マンガン=50/50(モ
ル比)からなる共重合体の10%水溶液100gを水1
00m1で希釈し、処理液とする。Example 1 100 g of a 10% aqueous solution of a copolymer consisting of acrylamide/manganese acrylate = 50/50 (molar ratio) was added to 1 part of water.
Dilute with 0.00ml to obtain a treatment solution.
実施例 2
ビニルピリジン/クロトン酸コバルト=30/70(モ
ル比)からなる共重合体の10%水溶液50gを水10
0m1で希釈し、処理液とする。Example 2 50 g of a 10% aqueous solution of a copolymer consisting of vinylpyridine/cobalt crotonate = 30/70 (mole ratio) was mixed with 10 g of water.
Dilute with 0ml and use as a treatment solution.
実施例 3
N−メチロールアクリルアミド/イタコン酸ニツケル=
70/30(モル比)からなる共重合体の10%水溶液
50gを水100m1で希釈し、処理液とする。Example 3 N-methylol acrylamide/nickel itaconate =
50 g of a 10% aqueous solution of a copolymer having a molar ratio of 70/30 is diluted with 100 ml of water to obtain a treatment liquid.
実施例 4 実施例1の処理液にリン酸ニアンモンを10g加える。Example 4 Add 10 g of ammonium phosphate to the treatment solution of Example 1.
実施例 5
実施例2の処理液にクエン酸10g及びリン酸ソーダ1
0gを加える。Example 5 10 g of citric acid and 1 portion of sodium phosphate were added to the treatment solution of Example 2.
Add 0g.
比較例 l
アクリルアミド/アクリル酸=50/50(モル比)か
らなる共重合体の10%水溶液100m1で希釈し、処
理液とする。Comparative Example 1 Dilute with 100 ml of a 10% aqueous solution of a copolymer consisting of acrylamide/acrylic acid = 50/50 (molar ratio) to obtain a treatment liquid.
比較例 2
ビニルピリジン/クロトン酸= 30/ 70(モル比
)からなる共重合体の10%水溶液を水100m1で希
釈後、クエン酸10g及びクエン酸ニアンモン10gを
加えて処理液とする。Comparative Example 2 A 10% aqueous solution of a copolymer consisting of vinylpyridine/crotonic acid = 30/70 (mole ratio) is diluted with 100 ml of water, and then 10 g of citric acid and 10 g of ammonium citrate are added to prepare a treatment liquid.
比較例 3 フエロシアン酸ソーダ 30g リン酸三ソーダ 10g クエン酸 10g 水 1000m1 よりなる処理液を調製する。Comparative example 3 Sodium ferocyanate 30g Trisodium phosphate 10g citric acid 10g Water 1000m1 Prepare a processing solution consisting of:
次に市販の酸化亜鉛〜樹脂分散系電子写真感光材料に画
像形成後、以上の各処理液で不感脂化処理して平版印刷
用マスターとし、湿し水として水道水を用いて印刷を行
なつた。Next, after forming an image on a commercially available zinc oxide/resin dispersion electrophotographic light-sensitive material, it is desensitized using each of the processing solutions mentioned above to prepare a lithographic printing master, and printing is performed using tap water as a dampening solution. Ta.
Claims (1)
からなる親水性共重合体を有効成分として含有する平版
印刷版用処理液。1. A lithographic printing plate processing liquid containing as an active ingredient a hydrophilic copolymer consisting of a basic polymerizable monomer and a polymerizable carboxylic acid metal salt.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12266276A JPS5952079B2 (en) | 1976-10-13 | 1976-10-13 | Processing liquid for lithographic printing plates |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12266276A JPS5952079B2 (en) | 1976-10-13 | 1976-10-13 | Processing liquid for lithographic printing plates |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5349506A JPS5349506A (en) | 1978-05-06 |
| JPS5952079B2 true JPS5952079B2 (en) | 1984-12-18 |
Family
ID=14841518
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP12266276A Expired JPS5952079B2 (en) | 1976-10-13 | 1976-10-13 | Processing liquid for lithographic printing plates |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5952079B2 (en) |
-
1976
- 1976-10-13 JP JP12266276A patent/JPS5952079B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5349506A (en) | 1978-05-06 |
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