JPS63131150A - Desensitization processing liquid - Google Patents

Desensitization processing liquid

Info

Publication number
JPS63131150A
JPS63131150A JP27807186A JP27807186A JPS63131150A JP S63131150 A JPS63131150 A JP S63131150A JP 27807186 A JP27807186 A JP 27807186A JP 27807186 A JP27807186 A JP 27807186A JP S63131150 A JPS63131150 A JP S63131150A
Authority
JP
Japan
Prior art keywords
salt
acid
parts
processing liquid
water
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
Application number
JP27807186A
Other languages
Japanese (ja)
Inventor
Masayuki Kuzuwata
葛綿 正行
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 JP27807186A priority Critical patent/JPS63131150A/en
Publication of JPS63131150A publication Critical patent/JPS63131150A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To enhance the desensitization power and buffer power of the titled processing liquid by using a specific processing liquid contg. inositol hexaphosphoric acid (salt) as a chief material. CONSTITUTION:(A) the inositol hexaphosphoric acid (salt), (B) colloidal silica, (C) water soluble Zr compd. (salt) and (D) org. acid (salt) are incorporated into the titled processing liquid. The grain size of the component B is preferably <=0.1mu and the content thereof is 1-5wt% of the component A. The component C consists of acetate or nitrate of Zr and the content thereof is preferably <=5wt% of the total amt. The component D consists of divalent and higher polybasic org. acid (salt) and the content thereof is preferably 0.5-10wt% of the total amt. A stable hydrophilic desensitized film is thereby early formed and further, the buffer power is improved, by which adaptability to neutral paper is improved.

Description

【発明の詳細な説明】 技免分災 本発明は電子写真型平版印刷原版の製版に用いられる不
感脂化処理液に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a desensitizing liquid used in plate making of electrophotographic lithographic printing original plates.

従来艮生 従来、電子写真型平版印刷原版の製版に用いられる不感
脂化処理液としてはフェロシアン塩及びリン酸塩を主体
とするものが反応速度が早く、且つ、不感脂化力も強い
ことから一般に用いられているが、熱や光に対する安定
性が良く、又シアンイオンを含有しているために排水規
制の対象となる欠点を有している。
Traditionally, the desensitizing treatment liquid used for plate making of electrophotographic lithographic printing original plates has been mainly composed of ferrocyan salts and phosphates because of its fast reaction rate and strong desensitizing power. Although it is commonly used, it has good stability against heat and light, and because it contains cyanide ions, it has the disadvantage of being subject to wastewater regulations.

そこでこれらの欠点を改良するため、フィチンa(イノ
シットヘキサリン酸)を主体とする不感脂化液が特公昭
45−24609号等で提案されているが、フィチン酸
単独では不感脂化力が弱く実用性に乏しかった。
Therefore, in order to improve these drawbacks, a desensitizing liquid containing phytic a (inositohexalic acid) as a main ingredient has been proposed in Japanese Patent Publication No. 45-24609, etc. However, phytic acid alone has no fat desensitizing ability. It was weak and impractical.

そこで更に特開昭53−83806号、同53−109
701号、同53−127003号、同54−4490
1号、同57−27840号等のようなフィチン酸を種
々の塩の形で用いたり、同58−579!11号のよう
に水溶性カチオンポリマーとのイオンコンプレックスを
形成し、見掛は上の保水性向上とはかっているが、未だ
不感脂化速度が遅く、エツチングプロセサーに1回通し
ただけでは満足すべき不感脂化力が得られなかった。
Therefore, Japanese Patent Publication Nos. 53-83806 and 53-109
No. 701, No. 53-127003, No. 54-4490
1, No. 57-27840, etc., or form an ionic complex with a water-soluble cationic polymer as in No. 58-579! However, the desensitization rate was still slow, and a satisfactory desensitization ability could not be obtained with just one pass through the etching processor.

更にこの欠点を改良すべく特開昭59−207290号
、同60−23098号、同60−23099号等では
反応速度を早めようとする提案もなされているが、未だ
満足すべきレベルに達していない。
Furthermore, in order to improve this drawback, proposals have been made in Japanese Patent Application Laid-open Nos. 59-207290, 60-23098, 60-23099, etc. to speed up the reaction speed, but this has not yet reached a satisfactory level. do not have.

一方これまで印刷用紙としてはロジン−硫酸バンドサイ
ズによる酸性紙が用いられてきたが。
On the other hand, acidic paper based on rosin-sulfuric acid band size has been used as printing paper so far.

近年紙の保存劣化の問題から炭酸カルシウムを填料とす
る中性紙に切り換りつつあり、その結果これまでの処理
液では耐久性に乏しく印刷汚れをひき起こして使えなく
なるという不具合が発生して来た。即ち中性紙を用いて
印刷した場合、充填剤として用いられる物質が湿し水中
に溶出して来るため、湿し水中のpH値が上昇し。
In recent years, due to the problem of paper deterioration during storage, there has been a shift to acid-free paper that uses calcium carbonate as a filler.As a result, conventional processing liquids have been found to lack durability and cause printing stains, making them unusable. It's here. That is, when printing is performed using neutral paper, substances used as fillers are eluted into the dampening water, and the pH value of the dampening water increases.

インキの乳化の促進及び版面の不感脂化膜の安定性が消
失する結果、汚れが発生するものと考えられる。
It is thought that staining occurs as a result of promotion of ink emulsification and loss of stability of the desensitized film on the plate surface.

目     的 本発明の目的は不感脂化速度を向上して不感脂化力を高
めると共に、バッファー力を高めて中性紙にも対応可能
にした不感脂化液を提供することである。
Purpose An object of the present invention is to provide a desensitizing liquid that improves the desensitizing speed and desensitizing power, and also increases the buffering power so that it can be applied to neutral paper.

構   成 本発明の不感脂化処理液はイノシットヘキサリン酸又は
その塩とコロイダルシリカと水溶性ジルコニウム化合物
と有機酸又はその塩とを含有することを特徴とするもの
である。
Composition The desensitizing treatment liquid of the present invention is characterized by containing inositohexalic acid or its salt, colloidal silica, a water-soluble zirconium compound, and an organic acid or its salt.

本発明の不感脂化処理液に用いられるイノシットヘキサ
リン酸(以下単にフィチン酸という)又はその塩は公知
の方法で合成でき、また市販品もある。フィチン酸塩と
してはブイチン酸の1.4位をCa、Ba、Mg、Co
、Mn等の2価の金属で置換したものが好ましい。
Inositohexalic acid (hereinafter simply referred to as phytic acid) or a salt thereof used in the desensitizing treatment solution of the present invention can be synthesized by a known method, and commercially available products are also available. As a phytate, the 1.4 position of butic acid is Ca, Ba, Mg, Co.
, Mn, and other divalent metals are preferred.

コロイダルシリカとしては粒経061μ以下のものが塗
布後の版面皮膜形成上好ましい。
The colloidal silica preferably has a grain size of 061 μm or less in terms of forming a film on the printing plate after coating.

水溶性ジルコニウム化合物としてはジルコニウムの無機
酸塩、有機酸塩が選ばれ、中でも酢酸塩、硝酸塩が不感
脂化反応速度を特に向上するので好ましい。
As the water-soluble zirconium compound, inorganic acid salts and organic acid salts of zirconium are selected, and acetates and nitrates are particularly preferred because they particularly improve the desensitization reaction rate.

有機酸又はその塩としてはクエン酸、マロン酸、アジピ
ン酸、タンニン酸、酒石酸、リンゴ酸、コハク酸等の多
塩基酸及びその塩が挙げられる。
Examples of organic acids or salts thereof include polybasic acids such as citric acid, malonic acid, adipic acid, tannic acid, tartaric acid, malic acid, and succinic acid, and salts thereof.

以上の成分の使用量はフィチン酸又はその塩については
1〜15%、コロイダルシリカについてはフィチン酸又
はその塩に対し1〜5%、水溶性ジルコニウム化合物に
ついては0.5〜5%有機酸又はその塩については0.
5〜10%が適当である。またこれらの成分を含む不感
脂化液のpHは3〜6が適当である。
The usage amount of the above components is 1 to 15% for phytic acid or its salt, 1 to 5% for colloidal silica to phytic acid or its salt, and 0.5 to 5% for water-soluble zirconium compound organic acid or 0 for the salt.
5 to 10% is appropriate. Further, the pH of the desensitizing liquid containing these components is preferably 3 to 6.

本発明においてフィチン酸又はその塩は不感脂化の主剤
として用いられ、コロイダルシリカ及び水溶性ジルコニ
ウム化合物はフィチン酸又はその塩の不感脂化反応速度
を向上して迅速な親水化(版面の被覆による)を行なう
助剤として用いられ、また有機酸又はその塩は中性紙に
対するバッファー力を高める助剤として用いられる。
In the present invention, phytic acid or its salt is used as the main agent for desensitization, and colloidal silica and water-soluble zirconium compounds improve the desensitization reaction rate of phytic acid or its salt, resulting in rapid hydrophilization (by coating the printing plate). ), and organic acids or their salts are used as aids to increase the buffering power for neutral paper.

本発明の不感脂化液には必要に応じて更に湿潤剤として
グリセリン、エチレングリコール類、ンルビトール等を
、防腐剤としてデヒドロ酢酸ソーダ、サリチル酸、ソル
ビン酸、カリウム、アミン類等を、親水化剤としてリン
酸及びその塩類等を、またpH調整剤としてKOH,N
aOH。
The desensitizing liquid of the present invention may further contain glycerin, ethylene glycols, nrubitol, etc. as wetting agents, sodium dehydroacetate, salicylic acid, sorbic acid, potassium, amines, etc. as preservatives, and hydrophilic agents as necessary. Phosphoric acid and its salts, etc., and KOH, N as a pH adjuster.
aOH.

NH4OH等を添加することができる。NH4OH etc. can be added.

以下に本発明を実施例によって説明する。なを部は全て
重量部である。
The present invention will be explained below by way of examples. All parts are by weight.

実施例1 フィチン酸ニマグネシウム塩     70部コロイダ
ルシリカ(平均粒経0.05μ)  3部酢酸ジルコニ
ウム          12部リンゴ酸      
         10部水            
           905部よりなる液をNaOH
でPH=4.5とした。
Example 1 Dimagnesium phytate 70 parts Colloidal silica (average particle size 0.05μ) 3 parts Zirconium acetate 12 parts Malic acid
10 parts water
A solution consisting of 905 parts of NaOH
The pH was set to 4.5.

実施例2 フィチン酸             80部コロイダ
ルシリカ(平均粒経0.05μ)  4部硝酸ジルコニ
ウム          10部コハク酸      
         15部水            
            891部よりなる液をNaO
HでpH=4.0とした。
Example 2 Phytic acid 80 parts Colloidal silica (average particle size 0.05μ) 4 parts Zirconium nitrate 10 parts Succinic acid
15 parts water
A solution consisting of 891 parts of NaO
The pH was adjusted to 4.0 with H.

実施例3 コロイダルシリカ(平均粒経0.05μ)  3部酢酸
ジルコニウム          10部酒石酸   
            12部水         
               915部よりなる液を
NaOHでpH=4.5とした。
Example 3 Colloidal silica (average particle size 0.05μ) 3 parts zirconium acetate 10 parts tartaric acid
12 parts water
A solution consisting of 915 parts was adjusted to pH=4.5 with NaOH.

実施例4 フィチン酸二ナトリウム塩      80部コロイダ
ルシリカ(平均粒経0.05μ)  3部硝酸ジルコニ
ウム          12部クエン酸      
         5部クエン酸二ナトリウム塩   
    5部水                  
      895部よりなる液をN a OHでpH
=4.0とした。
Example 4 Phytic acid disodium salt 80 parts Colloidal silica (average particle size 0.05μ) 3 parts Zirconium nitrate 12 parts Citric acid
5 parts citric acid disodium salt
5 parts water
A solution consisting of 895 parts was pH adjusted with NaOH.
= 4.0.

実施例5 フィチン酸二カルシウム塩      75部コロイダ
ルシリカ(平均粒経0.05μ)  3部酢酸ジルコニ
ウム          10部マレイン酸     
         15部水            
           897部よりなる液をNaOH
でpH=4.5とした。
Example 5 Phytic acid dicalcium salt 75 parts Colloidal silica (average particle size 0.05μ) 3 parts Zirconium acetate 10 parts Maleic acid
15 parts water
A solution consisting of 897 parts was diluted with NaOH.
The pH was set to 4.5.

実施例6 フイチン酸二マンガン塩       70部コロイダ
ルシリカ(平均粒経0.05μ)  3部酢酸ジルコニ
ウム          12部コハク酸      
         10部水            
           905部よりなる液をNa0)
lでpH=4.5とした。
Example 6 Dimanganese phytate 70 parts Colloidal silica (average particle size 0.05μ) 3 parts Zirconium acetate 12 parts Succinic acid
10 parts water
A solution consisting of 905 parts Na0)
The pH was adjusted to 4.5 with 1 liter of water.

比較例1 フィチン酸             70部水   
                     930部
よりなる液をNaOHでP)l=4.5とした。
Comparative Example 1 Phytic acid 70 parts water
A solution consisting of 930 parts was adjusted to P)l=4.5 with NaOH.

比較例2 フィチン酸             70部コロイダ
ルシリカ(平均粒経0.05μ)  3部水 よりなる液をNaOHでpH=4.5とした。
Comparative Example 2 A solution consisting of 70 parts of phytic acid, 3 parts of colloidal silica (average particle size 0.05 μm), and 3 parts of water was adjusted to pH=4.5 with NaOH.

比較例3 フィチン酸             70部コロイダ
ルシリカ(平均粒経0.05μ)  3部酢酸シリコニ
ウム          12部水         
               915部よりなる液を
NaOHでpH=4.5とした。
Comparative Example 3 Phytic acid 70 parts Colloidal silica (average particle size 0.05μ) 3 parts Siliconium acetate 12 parts Water
A solution consisting of 915 parts was adjusted to pH=4.5 with NaOH.

比較例4 フィチン酸二マグネシウム塩     70部水   
                    930部よ
りなる液をNaOHでpH=4.5とした。
Comparative Example 4 Dimagnesium phytate salt 70 parts water
A solution consisting of 930 parts was adjusted to pH=4.5 with NaOH.

比較例5 フィチン酸二マグネシウム塩     70部コロイダ
ルシリカ(平均粒経0.05μ)  3部水     
                  927部よりな
る液をNaOHでpH=4.5とした。
Comparative Example 5 Dimagnesium phytate salt 70 parts Colloidal silica (average particle size 0.05μ) 3 parts Water
A solution consisting of 927 parts was adjusted to pH=4.5 with NaOH.

比較例6 フィチン酸二マグネシウム塩     70部コロイダ
ルシリカ(平均粒経0.05μ)  3部酢酸ジルコニ
ウム          12部水         
              915部よりなる液をN
aOHでpH=4.5とした。
Comparative Example 6 Dimagnesium phytate salt 70 parts Colloidal silica (average particle size 0.05μ) 3 parts Zirconium acetate 12 parts Water
A solution consisting of 915 parts of N
The pH was adjusted to 4.5 with aOH.

以上のようにして得られた各不感脂化処理液について不
感脂化反応速度及び中性紙し二対する適応性を評価した
The desensitization reaction rate and suitability for use with neutral paper were evaluated for each desensitization treatment solution obtained as described above.

反応速度の評価: 湿式現像後の電子写真型平版印刷版(リコー社製すコー
ファクスマスターLDL)を、サンプルを入れたエツチ
ングプロセサー(リコー製)に1回通した後、直ちに平
版印刷機(リコー製A P 4600)にセットし、印
刷(中性紙使用)を行ない、印刷物の汚れ具合により評
価した。
Evaluation of reaction rate: After wet development, the electrophotographic planographic printing plate (Kofax Master LDL manufactured by Ricoh Co., Ltd.) was passed once through an etching processor (manufactured by Ricoh Co., Ltd.) containing the sample, and then immediately passed through an etching processor (manufactured by Ricoh Co., Ltd.) containing a sample. (AP 4600), printing was performed (using neutral paper), and evaluation was made based on the degree of staining of the printed matter.

O:全て汚れなし ×:全面地汚れあり 中性紙に対する適応性: 反応速度の評価の場合と同様、湿式現像後の平版印刷版
を、サンプルを入れたエツチングプロセサーに3回通し
て完全に不感脂化した後。
O: No stains at all ×: Full background stains Applicability to neutral paper: As in the reaction rate evaluation, the lithographic printing plate after wet development was passed through the etching processor containing the sample three times to ensure complete insensitivity. After turning into fat.

水5:サンプル1(容量比)の割合で配合した湿し水を
用いて平版印刷を行なった際の汚れの発生する迄の印刷
枚数で評価した。
Evaluation was made based on the number of printed sheets until staining occurred when lithographic printing was performed using dampening water mixed in a ratio of water 5:sample 1 (volume ratio).

0 : 3000枚以上汚れず、適応性良好x : 2
00〜300枚で汚れ発生し、適応性不良効−−−教 以上の如く本発明の不感脂化処理液はフィチン酸又はそ
の塩にコロイダルシリカ及び水溶性ジルコニウム化合物
を結合せることにより反応速度が早く安定な親水性不感
脂化膜を形成し、さらには有機酸又はその塩を添加する
ことにより中性紙に対する適応性を向上し、印刷汚れを
生じることがない等の利点を有している。
0: Over 3,000 sheets without staining, good adaptability x: 2
00 to 300 sheets, resulting in poor adaptability.As described above, the desensitizing treatment solution of the present invention has a reaction rate that increases by combining colloidal silica and a water-soluble zirconium compound with phytic acid or its salt. It has the advantage of quickly forming a stable hydrophilic and fat-insensitive film, and by adding an organic acid or its salt, it improves adaptability to neutral paper and does not cause printing stains. .

Claims (1)

【特許請求の範囲】 1、イノシットヘキサリン酸又はその塩とコロイダルシ
リカと水溶性ジルコニウム化合物と有機酸又はその塩と
を含有することを特徴とする不感脂化処理液。 2、前記コロイダルシリカの粒経が0.1μ以下であり
、且つその含有量がイノシットヘキサリン酸又はその塩
の1〜5重量%である特許請求の範囲第1項の不感脂化
処理液。 3、前記水溶性ジルコニウム化合物の含有量が全量の5
重量%以下である特許請求の範囲第1項の不感脂化処理
液。 4、有機酸又はその塩が2価以上の多塩基性有機酸又は
その塩であり、且つその含有量が全量の0.5〜10重
量%である特許請求の範囲第1項の不感脂化処理液。
[Scope of Claims] 1. A desensitizing treatment liquid characterized by containing inositohexalic acid or its salt, colloidal silica, a water-soluble zirconium compound, and an organic acid or its salt. 2. The desensitizing treatment liquid according to claim 1, wherein the colloidal silica has a grain size of 0.1 μ or less, and its content is 1 to 5% by weight of inositohexalic acid or its salt. . 3. The content of the water-soluble zirconium compound is 5 of the total amount.
% or less by weight of the desensitizing liquid according to claim 1. 4. Desensitization according to claim 1, wherein the organic acid or its salt is a divalent or higher polybasic organic acid or its salt, and the content thereof is 0.5 to 10% by weight of the total amount. processing liquid.
JP27807186A 1986-11-20 1986-11-20 Desensitization processing liquid Pending JPS63131150A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP27807186A JPS63131150A (en) 1986-11-20 1986-11-20 Desensitization processing liquid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP27807186A JPS63131150A (en) 1986-11-20 1986-11-20 Desensitization processing liquid

Publications (1)

Publication Number Publication Date
JPS63131150A true JPS63131150A (en) 1988-06-03

Family

ID=17592240

Family Applications (1)

Application Number Title Priority Date Filing Date
JP27807186A Pending JPS63131150A (en) 1986-11-20 1986-11-20 Desensitization processing liquid

Country Status (1)

Country Link
JP (1) JPS63131150A (en)

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