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JPS6039035B2 - Processing liquid for lithographic printing plates - Google Patents
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JPS6039035B2 - Processing liquid for lithographic printing plates - Google Patents

Processing liquid for lithographic printing plates

Info

Publication number
JPS6039035B2
JPS6039035B2 JP13379076A JP13379076A JPS6039035B2 JP S6039035 B2 JPS6039035 B2 JP S6039035B2 JP 13379076 A JP13379076 A JP 13379076A JP 13379076 A JP13379076 A JP 13379076A JP S6039035 B2 JPS6039035 B2 JP S6039035B2
Authority
JP
Japan
Prior art keywords
acid
lithographic printing
processing liquid
aqueous solution
methacrylic acid
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
Application number
JP13379076A
Other languages
Japanese (ja)
Other versions
JPS5359502A (en
Inventor
正行 葛綿
元 町田
宏 田村
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.)
Ricoh Co Ltd
Original Assignee
Ricoh 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 Ricoh Co Ltd filed Critical Ricoh Co Ltd
Priority to JP13379076A priority Critical patent/JPS6039035B2/en
Publication of JPS5359502A publication Critical patent/JPS5359502A/en
Publication of JPS6039035B2 publication Critical patent/JPS6039035B2/en
Expired legal-status Critical Current

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  • 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塩一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 subsalt oxide monoresin dispersion system.

更に詳しくは酸化亜塩一樹脂分散系を光電導層として基
紙上に塗工した電子写真記録紙をオフセット平版EO刷
用マスターとして用いる場合に使用される不感脂化処理
液に関する。光導電性酸化亜塩をシリコン樹脂、アクリ
ル樹脂など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
部を不惑脂化処理した平版印刷用マスタとして使用する
ことが知られている。
More specifically, the present invention relates to a desensitizing solution used when an electrophotographic recording paper in which a subsalt oxide monoresin dispersion system is coated on a base paper as a photoconductive layer is used as a master for offset lithographic EO printing. Lithographic printing in which an image is formed on an electrophotographic material having a photoconductive layer in which a photoconductive subsalt oxide is dispersed in an insulating resin such as a silicone resin or an acrylic resin by a conventional method, and then non-image areas are treated to make the non-image area fat-free. It is known to be used as a master.

従来このような処理に使用される不感脂化液はフェロシ
アン化合物、燐酸塩等の不感脂化剤、これに有機酸、無
機酸の様なPH調整剤、さらにCMC、グリセリン、ア
ルギン酸、アラビアゴム等の湿潤剤を主体として含有す
るものである。
Desensitizing liquids conventionally used in such treatments include desensitizing agents such as ferrocyanic compounds and phosphates, PH adjusters such as organic acids and inorganic acids, and CMC, glycerin, alginic acid, and gum arabic. It mainly contains a wetting agent such as.

しかしフェロシアン化物は光による劣化が著しく、この
ため液の品質低下(変色、沈澱など)のみならず、平版
印刷版の非画像部にいわゆるギャ一目汚れや地汚れを発
生させるし、公害の面からもその使用は避けることが望
まれる。一方フェロシアン化物を含有しない不惑脂化液
も提案されているが、地汚れはフェロシアン化物よりも
むしろ発生し易いばかりかエッチングラムをも招く結果
となっており実用にとほしいものばかりである。
However, ferrocyanide is significantly degraded by light, and this not only causes a decline in the quality of the liquid (discoloration, precipitation, etc.), but also causes so-called smudges and background stains in the non-image areas of planographic printing plates, resulting in pollution. It is recommended that its use be avoided. On the other hand, non-fattening liquids that do not contain ferrocyanide have been proposed, but they are not only more likely to cause scumming than ferrocyanide, but also result in etching marks, so these are things that should be put into practical use. .

本発明は以上の欠点を除去したものであって、フェロシ
ァン化物を含有することなくして、地汚れのない鮮明な
印刷物を供しうる平版印刷版用処理液を提供するもので
ある。
The present invention eliminates the above-mentioned drawbacks and provides a processing liquid for lithographic printing plates that does not contain ferrocyanide and can provide clear printed matter without background stains.

即ち本発明はメタクリル酸重合体若しくはメタクリル酸
と特定の単量体との共重合体に特定の金属塩を反応させ
た化合物を含むものである。
That is, the present invention includes a compound obtained by reacting a methacrylic acid polymer or a copolymer of methacrylic acid and a specific monomer with a specific metal salt.

メタクリル酸と重合させる単量体は下記の一般式で示さ
れる。(た)、し、X,:日,CH3,COO日,OC
H3,X2:日,CH3,COO日,OCH3,Y,:
日,CH3,Y2:COO日,COOC2日5,COO
C3日60日,C比COO日,’Cは, 。
The monomer to be polymerized with methacrylic acid is represented by the following general formula. (Ta), Shi, X, :Sun, CH3, COO Sun, OC
H3, X2: day, CH3, COO day, OCH3, Y,:
Day, CH3, Y2: COO Day, COOC2 Day 5, COO
C3 days 60 days, C ratio COO days, 'C is.

C。CH3,CH2CH3,COOCH3, COOC2日40日 これら単量体は1種又は2種以上使用される。C. CH3, CH2CH3, COOCH3, COOC2 days 40 days One or more of these monomers may be used.

なお前記重合体若しくは共重合体中のメタクリル酸と他
の単量体の比は100対0(即ちメタクリル酸のホモポ
リマー)〜5対99節こ10政寸0〜70対30である
ことが好ましい。前記重合体若しくは共重合体にMn,
Fe,Ni,Co,Zn,Mg,およびZrの群から選
ばれる金属塩を反応せた化合物が本発明の処理液の主成
分となる。金属塩としては、有機酸塩則ちカルボン酸の
塩がよく、例えば酢酸コバルト、酢酸マンガン、酢酸ニ
ッケル、酢酸亜鉛、酢酸マグネシウム、酢酸鉄、酢酸ジ
ルコニウムなどの塩を挙げることができる。前記重合体
若しくは共重合体と金属塩を反応させた化合物は金属塩
含有重合単位が30モル%以下が好ましく、平版印刷用
処理液に0.1〜1の重量%含有させる。反応生成物の
濃度が0.1重量%以下では不感脂化能力を充分に持た
ない処理液となり、平版印刷版非画像部に地汚れが生じ
易く、きれいな画像を持つ印刷物が得られない。一方反
応生成物の濃度が10重量%以上では処理液が高粘度と
なり取扱い上好ましくない。本発明の処理液には前記し
た反応生成物の他にリン酸第一アンモニウム、リン酸第
二アンモニウム、リン酸ソーダ、リン酸などのPH緩衝
剤、クエン酸、マロン酸、乳酸、酒石酸等の有機酸又は
燐酸、塩酸等の無機酸のPH調整剤、さらにCMC、グ
リセリン等の親水性化合物などの一般の処理液に用いら
れる種々の添加剤を含有させることができる。
The ratio of methacrylic acid to other monomers in the polymer or copolymer may be 100:0 (i.e., a homopolymer of methacrylic acid) to 5:99, or 0 to 70:30. preferable. The polymer or copolymer contains Mn,
A compound obtained by reacting a metal salt selected from the group of Fe, Ni, Co, Zn, Mg, and Zr is the main component of the treatment liquid of the present invention. The metal salt is preferably an organic acid salt, ie, a carboxylic acid salt, and includes salts of cobalt acetate, manganese acetate, nickel acetate, zinc acetate, magnesium acetate, iron acetate, zirconium acetate, and the like. The compound obtained by reacting the polymer or copolymer with a metal salt preferably has a metal salt-containing polymer unit of 30 mol% or less, and is contained in the lithographic printing processing liquid in an amount of 0.1 to 1% by weight. If the concentration of the reaction product is less than 0.1% by weight, the processing liquid will not have sufficient desensitizing ability, and the non-image areas of the lithographic printing plate will be prone to scumming, making it impossible to obtain printed matter with clear images. On the other hand, if the concentration of the reaction product is 10% by weight or more, the treatment liquid will have a high viscosity, which is unfavorable for handling. In addition to the reaction products described above, the treatment solution of the present invention contains PH buffers such as primary ammonium phosphate, secondary ammonium phosphate, sodium phosphate, and phosphoric acid, as well as citric acid, malonic acid, lactic acid, and tartaric acid. Various additives used in general processing liquids, such as a pH adjuster of an organic acid or an inorganic acid such as phosphoric acid or hydrochloric acid, and a hydrophilic compound such as CMC or glycerin, can be contained.

本発明の処理液は不感脂化液として使用する場合、前述
した濃度でよいが、不感脂化後の平版印刷版に溢し水と
して使用する場合は更に2〜10倍程度に希釈して使用
することができる。
When the processing solution of the present invention is used as a desensitizing solution, it may be used at the concentration mentioned above, but when used as overflow water for a lithographic printing plate after desensitization, it is further diluted to about 2 to 10 times. can do.

以上の通り、本発明はフェロシアン化物を含有していな
いので、フェロシアン化物のもつ不利益な点は解消され
、しかも処理液としての性能はフェロシアン化物を含有
した処理液、あるいは含有しない処理液のいずれの性能
よりも優れたものであり、実用性の高い処理液である。
As described above, since the present invention does not contain ferrocyanide, the disadvantages of ferrocyanide are eliminated, and the performance as a treatment liquid is better than that of a treatment liquid containing ferrocyanide or a treatment that does not contain ferrocyanide. It has better performance than any other liquid and is a highly practical treatment liquid.

比較例 1フエロシアンソーダ 30
タリン酸(m)ソーダ 309クエン
酸 10夕グリセリン
10夕上記処方を水1000の‘に均
一に溶解する。
Comparative example 1 Ferocyan soda 30
Talic acid (m) soda 309 Citric acid 10 Glycerin
10 minutes The above formulation was uniformly dissolved in 1,000 ml of water.

比較例 2フエロシアンソーダ 20
9リン酸(皿)ソーダ 10タリン酸(ロ
)アンモニウム 10タCMC
I夕クエン酸
7夕上記処方を水1000の‘に均一に熔解する。
Comparative example 2 Ferocyan soda 20
9 Sodium phosphate 10 Ammonium talate 10 CMC
I citric acid
After 7 days, the above formulation was uniformly dissolved in 1,000 ml of water.

比較例 3クロムミヨーバン 30
タ硝酸アンモニウム 20タリン酸
(m)アンモニウム 30タグリセリン
20夕上記処方を水100
0机上に均一に熔解する。
Comparative example 3 Chrome alum 30
Ammonium talinate 20 Ammonium talinate 30 Taglycerin
20 pm Add the above prescription to 100 ml of water.
0 Melt evenly on the desk.

実施例 1メタクリル酸/アクリル酸=50/50%モ
ル比の共重合体5%水溶液500のとに酢酸Col%水
溶液200の‘を滴下しながら加え、80〜9000で
6時間反応させる。
Example 1 200% acetic acid Col aqueous solution was added dropwise to 500% aqueous solution of a 5% copolymer having a molar ratio of methacrylic acid/acrylic acid = 50/50%, and the mixture was reacted at 80 to 9000 for 6 hours.

反応終了後メタノール中に滴下し酢酸と生成物を炉8U
し、生成物を0.5%水溶液にする。実施例 2メタク
リル酸/ヒドロキシヱチルアクリレート=60/40%
モル比の共重合体50%水溶液400の‘中に酢酸Mn
o.5%水溶液400叫を加え、80〜9000で8時
間反応させる。
After the reaction was completed, the acetic acid and the product were added dropwise to methanol in a furnace of 8U.
and make the product into a 0.5% aqueous solution. Example 2 Methacrylic acid/Hydroxyethyl acrylate = 60/40%
Mn acetate in a 50% copolymer aqueous solution with a molar ratio of 400
o. Add 400 ml of 5% aqueous solution and react at 80-9000 ml for 8 hours.

反応終了後実施例1同様にして得られた生成物を1%水
溶液にする。実施例 3 メタクリル酸/メチルビニルェーテル=70/30%モ
ル比の共重合体50%水溶液400叫中に酢酸八4g0
.3%水溶液を400ののロえ、80〜9000で8時
間反応後、実施例1同様にして生成物を得た後、1%水
溶液にする。
After the reaction was completed, the product obtained in the same manner as in Example 1 was made into a 1% aqueous solution. Example 3 84 g of acetic acid was added to 400 g of a 50% aqueous solution of a copolymer with a molar ratio of methacrylic acid/methyl vinyl ether = 70/30%.
.. A 3% aqueous solution was poured at 400° C., and after reaction for 8 hours at 80-9000° C., a product was obtained in the same manner as in Example 1, and then converted into a 1% aqueous solution.

実施例 4 メタクリル酸/アクリル酸=70/30%モル比の共重
合体5%水溶液500地中に酢酸Nil%水溶液200
の‘を加え、80〜9000で6時間反応し実施例1同
様にして生成物を得た後、1%水溶液にする。
Example 4 500% aqueous solution of copolymer with methacrylic acid/acrylic acid = 70/30% molar ratio 500% aqueous solution of Nil acetate 200%
' was added and reacted for 6 hours at 80 to 9000°C to obtain a product in the same manner as in Example 1, which was then made into a 1% aqueous solution.

実施例 5メタクリル酸/クロトン酸=40/60%モ
ル比の共重合体5%水溶液500の‘中に酢酸Col%
水溶液200のとを加え、80〜9000で6時間反応
し実施例1同様にして生成物を得た後、1%水溶液とす
る。
Example 5 Acetic acid Col% in 500% aqueous copolymer solution with methacrylic acid/crotonic acid = 40/60% molar ratio
A 200% aqueous solution was added, and the mixture was reacted for 6 hours at 80 to 9,000 °C to obtain a product in the same manner as in Example 1, followed by a 1% aqueous solution.

実施例 6メタクリル酸/クロトン酸/アクリル酸=4
0/30/30モル比の共重合体5%水溶液500の‘
に酢酸Mn,0.5%水溶液400の‘を加え、80〜
9000で6時間反応し、実施例1と同様にして生成物
を得る。
Example 6 Methacrylic acid/crotonic acid/acrylic acid = 4
500' of 5% aqueous copolymer solution with 0/30/30 molar ratio
Add 400' of Mn acetate, 0.5% aqueous solution to
9000 for 6 hours, and the same procedure as in Example 1 was carried out to obtain a product.

得られた生成物を1%水溶液にする。以上の各処理液を
脱脂綿にふくませてリコーフアクスマスター製版後ハン
ドエッチングを行ない、リコーオフセットAP−151
0で印刷した結果を示す。
The product obtained is made into a 1% aqueous solution. Ricoh Offset AP-151
The result of printing with 0 is shown.

Claims (1)

【特許請求の範囲】 1 メタクリル酸重合体若しくはメタクリル酸と下記の
一般式で示される1種又は2種以上の単量体との共重合
体に、Mn,Fe,Ni,Co,Zn,Mg,およびZ
rの群から選ばれる1種の金属塩を反応させた化合物を
含み、かつ上記化合物中の金属塩含有重合単位が30モ
ル%以下であることを特徴とする平版印刷用処理液。 ▲数式、化学式、表等があります▼
[Claims] 1. Mn, Fe, Ni, Co, Zn, Mg in a methacrylic acid polymer or a copolymer of methacrylic acid and one or more monomers represented by the following general formula. , and Z
A lithographic printing processing liquid comprising a compound reacted with one kind of metal salt selected from the group r, and wherein the metal salt-containing polymerized unit in the compound is 30 mol % or less. ▲Contains mathematical formulas, chemical formulas, tables, etc.▼
JP13379076A 1976-11-09 1976-11-09 Processing liquid for lithographic printing plates Expired JPS6039035B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13379076A JPS6039035B2 (en) 1976-11-09 1976-11-09 Processing liquid for lithographic printing plates

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13379076A JPS6039035B2 (en) 1976-11-09 1976-11-09 Processing liquid for lithographic printing plates

Publications (2)

Publication Number Publication Date
JPS5359502A JPS5359502A (en) 1978-05-29
JPS6039035B2 true JPS6039035B2 (en) 1985-09-04

Family

ID=15113062

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13379076A Expired JPS6039035B2 (en) 1976-11-09 1976-11-09 Processing liquid for lithographic printing plates

Country Status (1)

Country Link
JP (1) JPS6039035B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5465606A (en) * 1977-11-04 1979-05-26 Asahi Chemical Ind Desensitizing agent for flat plate

Also Published As

Publication number Publication date
JPS5359502A (en) 1978-05-29

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