JPH0517879B2 - - Google Patents

Info

Publication number
JPH0517879B2
JPH0517879B2 JP60058798A JP5879885A JPH0517879B2 JP H0517879 B2 JPH0517879 B2 JP H0517879B2 JP 60058798 A JP60058798 A JP 60058798A JP 5879885 A JP5879885 A JP 5879885A JP H0517879 B2 JPH0517879 B2 JP H0517879B2
Authority
JP
Japan
Prior art keywords
acid
desensitizing
solution
processing
silicic 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 - Lifetime
Application number
JP60058798A
Other languages
Japanese (ja)
Other versions
JPS61215089A (en
Inventor
Yasuhiro Aizawa
Shoji Tatsuki
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.)
Mitsubishi Paper Mills Ltd
Original Assignee
Mitsubishi Paper Mills 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 Mitsubishi Paper Mills Ltd filed Critical Mitsubishi Paper Mills Ltd
Priority to JP5879885A priority Critical patent/JPS61215089A/en
Publication of JPS61215089A publication Critical patent/JPS61215089A/en
Publication of JPH0517879B2 publication Critical patent/JPH0517879B2/ja
Granted legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41NPRINTING PLATES OR FOILS; MATERIALS FOR SURFACES USED IN PRINTING MACHINES FOR PRINTING, INKING, DAMPING, OR THE LIKE; PREPARING SUCH SURFACES FOR USE AND CONSERVING THEM
    • B41N3/00Preparing for use and conserving printing surfaces
    • B41N3/08Damping; Neutralising or similar differentiation treatments for lithographic printing formes; Gumming or finishing solutions, fountain solutions, correction or deletion fluids, or on-press development

Landscapes

  • Printing Plates And Materials Therefor (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

(A) 産業上の利用分野 本発明は電子写真オフセツトマスターの不感脂
化処理に使用される処理液に関する。 (B) 従来技術 電子写真オフセツトマスターは導電性支持体上
に酸化亜鉛等の光導電性物質を樹脂結着剤中に分
散された感光層を有し、当該層上に帯電、露光、
現像、定着の各工程を経た後感光層上に親油性画
像を形成させ、不感脂化処理液で処理して作用さ
れる。 従来電子写真オフセツトマスターに使用される
処理液はフエロシアン塩やフエリシアン塩等のヘ
キサシアノ鉄塩を主成分とするものが使用されて
いた。特にヘキサシアノ鉄塩を主成分とする処理
液は処理条件による寛容度が広く、例えば自動化
された処理装置で1回通しや2回通しを行なつて
もまた処理液を手で版材に塗布(ハンドエツチン
グ)しても良好のる印刷物の与えることが出来
た。但しヘキサシアノ鉄塩は熱や光によつて分解
して、遊離のシアンを発生する場合があり、ヘキ
サシアノ鉄塩を主体とする不感脂化処理液は公害
上の問題点を有していた。このためイノシツトヘ
キサリン酸エステル又はその塩などを主体とした
シアンフリータイプの不感脂化処理液が提案され
ているがまだ充分満足すべき品質のものは完成さ
れていない。 イノシツトヘキサリン酸エステル又はその塩を
不感脂化主剤として使用した場合の欠点として
は、不感脂化の成膜速度が遅い点である。具体例
な事例として不感脂化処理液を脱脂綿やスポンジ
等に含ませて版の表面に手塗りすることによつて
行うハンドエツチングでは不感脂化処理液が充分
に版面に塗布されるため、シアンタイプとの不感
脂化処理能力の差はそれほど目立たないが、自動
化された不感脂化処理装置(例えば三菱製紙製エ
ツチングコンバーターOH−11等)による処理で
は、シアンタイプとの能力差が見られ、印刷物に
汚れを生ずる場合があつた。 一方この様な点を考慮して成膜速度の速い処理
液が特開昭59−207290号公報に開示されている。
これはイノシツトヘキサリン酸エステル又はその
塩とSiOH基を有する粒径40mμ以下の酸性コロ
イダル硅酸を組合わせたもので、即時の成膜性は
良好である。しかしながらこの処理液を自動化さ
れた不感脂化処理装置で2回通しをした場合で手
や処理液を版材面に塗布したような場合には画像
部(トナー部)まで不感脂化処理が行なわれてし
まい、画像部にインキが付着しないという現象を
生じてしまう欠点を有していた。 (C) 発明の目的 本発明はイノシツトヘキサリン酸エステル又は
その塩などのシアンフリータイプの処理液が有す
る不感脂化の成膜速度の遅い点を改良するもので
あり、また製造が容易でかつ品質が安定であり、
さらには自動化された不感脂化処理装置の1回通
しで印刷物の地汚れがなく、インキ乗りの良好な
平版印刷用不感脂化処理液を提供することを目的
とする。 (D) 発明の構成 本発明者等は上記の問題点を解決すべく鋭意検
討した結果、次のような方法を見い出し本発明を
完成するに至つた。 即ち本発明は不感脂化処理液中にリン酸二水素
塩及びSiOH基を有する粒径40mμ以下の酸性コ
ロイド硅酸を含有せしめ、該液のPHを3.0〜6.0に
したものよりなる。 本発明で言うリン酸二水素塩とは、例えば、
NaH2PO4、KH2PO4、NH4H2PO4、Ca
(H2PO42、Mg(H2PO42、Al(H2PO43、Fe
(H2PO43等が挙げられ、処理液中の濃度は1.0
g/〜300g/が好ましく、特に好ましい範
囲は5.0g/〜50g/である。この範囲より
少ない量では不感脂化能力が充分でなく印刷物に
地汚れを生ずるようになり、この範囲より多い
と、不感脂化能力が強くなりすぎてインキ乗りが
悪くなる。 一方SiOH基を有する粒径40mμ以下の酸性コ
ロイド硅酸とはいわゆるコロイダルシリカ、水ガ
ラスなどと称せられるもの及びこれらの表面改質
をしたものなどである。これらの処理液中に添加
すべき濃度は0.1g/〜30g/が好ましく、
特に好ましい範囲は1.0g/〜20g/である。
この範囲が好ましい理由は上述と同じである。 本発明の平版印刷版用不感脂化処理液に於ける
実施態様には上記成分の他に、前記した親水性高
分子、オキシカルボン酸又はその塩、及びキレー
ト剤の少なくとも一種を含有することを包含す
る。 親水性高分子とは、水溶性で保護コロイド性を
有し、親水性層の保護、補強効果を与えるもので
あり、その例としてはアラビアゴム、アルギン酸
塩、ポリアクリル酸塩、ポリビニルアルコール、
ポリビニルピロリドン、カルボキシメチルセルロ
ース又はその塩、デキストリン、変成デンプン等
で、処理液中の濃度は0.1g/〜50g/が好
ましく、特に好ましい範囲は1.0g/〜30g/
である。 オキシカルボン酸とは、サリチル酸、マルデル
酸、乳酸、グルコン酸、アスコルビン酸、クエン
酸等であり、処理液中の濃度は0.5g/〜100
g/が好ましいが、特に好ましい範囲は1g/
〜40g/である。 キレート剤は処理液の不感脂化能力をさらに向
上させ、又本発明の処理液を希釈して給湿液とし
て使用する際に印刷中の地汚れを防止する能力を
有する物質を指し、その例としてはエチレンジア
ミン四酢酸、ジエチレントリアミン五酢酸、イミ
ノ二酢酸、ニトリロ三酢酸、ピロリン酸、トリリ
ン酸等々のナトリウム、カリウム、アンモニウム
塩等があり、処理液中の濃度は0.1g/〜100
g/が好ましく、特に好ましい範囲は5g/
〜50g/である。 さらには、処理液の酸性度調整剤として無機及
び有機の酸や塩基性物質、及び公知の防腐剤、防
錆剤等を適当量添加して使用することが出来る。 本発明の処理液を使用するに当たり、液のPHは
3.0〜6.0の範囲が望ましい。又、本処理液を水で
4〜10倍に希釈して給湿液としても使用出来る。 次に実施例、比較例により本発明を説明する。 実施例 1 リン酸二水素カリウム 3.0g 酸性コロイド珪酸(粒径20mμ) 0.2g クエン酸二アンモニウム 1.0g グリセリン 4.0g 水を加えて 100g を充分溶解し、溶液のPHを4.5とした。 実施例 2 リン酸二水素アンモニウム 3.0g 酸性コロイド珪酸(粒径20mμ) 0.2g グルコン酸ナトリンム 1.5g グリセリン 4.0g 水を加えて 100g を充分溶解し、溶液のPHを4.5とした。 実施例 3 リン酸二水素カルシウム 3.0g 酸性コロイド珪酸(粒径20mμ) 0.2g フタル酸−カリウム 1.0g グリセリン 4.0g 水を加えて 100g を充分溶解し、溶液のPHHを4.5とした。 比較例 1 イノシツトヘキサリン酸エステル 3.0g 酸性コロイド硅酸(粒径20mμ) 0.2g クエン酸二アンモニウム 1.0g グリセリン 4.0g 水を加えて 100g を充分溶解し、溶液のPHを4.5とした。 比較例 2 リン酸−水素二ナトリウム 3.0g 酸性コロイド珪酸(粒径20mμ) 0.2g グルコン酸ナトリウム 1.0g グリセリン 4.0g 水を加えて 100g を充分溶解し、溶液のPHを4.5とした。 比較例 3 リン酸二水素カリウム 3.0g 酸性コロイド珪酸(粒径50mμ) 0.2g クエン酸二アンモニウム 1.0g グリセリン 4.0g 蒸留水 91.8g を充分溶解し、溶液のPHHを6.1とした。 一方、市販の電子写真オフセツトマスターを常
法に従つて画像を形成させた後、夫々の処理液で
エツチングコンバーターOH−11(三菱製紙製)
にて1回通しの不感脂化処理を行なつた。また給
湿水は同処理液1に対し水道水9の容量比で希釈
した液を使用した。 表に小型オフセツト印刷機(トーコーモデル
8:10:東京航空計器製)で印刷を行つた結果を
示す。
(A) Industrial Application Field The present invention relates to a processing liquid used for desensitizing an electrophotographic offset master. (B) Prior art An electrophotographic offset master has a photosensitive layer on a conductive support in which a photoconductive substance such as zinc oxide is dispersed in a resin binder, and the layer is charged, exposed, and
After the development and fixing steps, a lipophilic image is formed on the photosensitive layer and treated with a desensitizing solution. Conventionally, processing liquids used in electrophotographic offset masters have been mainly composed of hexacyanoferric salts such as ferrocyanate and ferricyanide salts. In particular, processing liquids containing iron hexacyanosalts as a main component have a wide latitude depending on the processing conditions; for example, even if an automated processing device performs one or two passes, the processing liquid can also be manually applied to the plate material. Even with hand etching, it was possible to produce prints with good adhesion. However, hexacyanoferric salts may be decomposed by heat or light to generate free cyanide, and desensitizing treatment liquids containing hexacyanoferric salts as a main component have had problems in terms of pollution. For this reason, a cyanide-free type desensitizing solution containing inositohexalic acid ester or its salt as a main ingredient has been proposed, but a solution of sufficiently satisfactory quality has not yet been completed. A disadvantage of using inositohexalic acid ester or its salt as a desensitizing main agent is that the rate of desensitizing film formation is slow. A specific example is hand etching, which involves soaking absorbent cotton or sponge in a desensitizing solution and hand-painting it onto the surface of the plate. The difference in desensitization processing ability with the cyan type is not so noticeable, but when processed using automated desensitization processing equipment (e.g. Mitsubishi Paper Etching Converter OH-11, etc.), there is a difference in ability with the cyan type. There were cases where printed matter was smudged. On the other hand, in consideration of these points, a processing solution with a high film formation rate is disclosed in Japanese Patent Application Laid-Open No. 59-207290.
This is a combination of inositohexalic acid ester or its salt and acidic colloidal silicic acid having a SiOH group and a particle size of 40 mμ or less, and has good instant film-forming properties. However, if this processing liquid is passed twice through an automated desensitizing device and the processing liquid is applied to the surface of the plate material by hand, the desensitizing process will not be applied to the image area (toner area). This has the disadvantage that the ink does not adhere to the image area. (C) Purpose of the Invention The present invention aims to improve the slow desensitizing film formation rate of cyanide-free type processing solutions such as inositohexalic acid esters or their salts, and is easy to manufacture. and the quality is stable,
A further object of the present invention is to provide a desensitizing liquid for lithographic printing that does not cause background smudges on printed matter and has good ink coverage in one pass through an automated desensitizing device. (D) Structure of the Invention As a result of intensive study to solve the above problems, the inventors discovered the following method and completed the present invention. That is, the present invention comprises a desensitizing solution containing dihydrogen phosphate and acidic colloidal silicic acid having a SiOH group and a particle size of 40 mμ or less, and adjusting the pH of the solution to 3.0 to 6.0. The dihydrogen phosphate referred to in the present invention is, for example,
NaH 2 PO 4 , KH 2 PO 4 , NH 4 H 2 PO 4 , Ca
(H 2 PO 4 ) 2 , Mg (H 2 PO 4 ) 2 , Al (H 2 PO 4 ) 3 , Fe
(H 2 PO 4 ) 3, etc., and the concentration in the treatment liquid is 1.0
g/~300 g/ is preferred, and a particularly preferred range is 5.0 g/~50 g/. If the amount is less than this range, the desensitizing ability will not be sufficient and scumming will occur on printed matter, and if it is more than this range, the desensitizing ability will be too strong and ink coverage will be poor. On the other hand, acidic colloidal silicic acid having a SiOH group and having a particle size of 40 mμ or less includes so-called colloidal silica, water glass, etc., and surface-modified products thereof. The concentration to be added to these processing solutions is preferably 0.1g/~30g/,
A particularly preferred range is 1.0 g/-20 g/.
The reason why this range is preferable is the same as mentioned above. In an embodiment of the desensitizing treatment liquid for lithographic printing plates of the present invention, in addition to the above-mentioned components, it may contain at least one of the above-mentioned hydrophilic polymer, oxycarboxylic acid or its salt, and chelating agent. include. Hydrophilic polymers are water-soluble, have protective colloidal properties, and provide a protective and reinforcing effect to the hydrophilic layer. Examples include gum arabic, alginates, polyacrylates, polyvinyl alcohol,
Polyvinylpyrrolidone, carboxymethyl cellulose or its salt, dextrin, modified starch, etc., and the concentration in the treatment liquid is preferably 0.1 g/~50 g/, and a particularly preferable range is 1.0 g/~30 g/
It is. Oxycarboxylic acids include salicylic acid, malderic acid, lactic acid, gluconic acid, ascorbic acid, citric acid, etc., and the concentration in the treatment liquid is 0.5g/~100
g/, but a particularly preferable range is 1 g/
~40g/. A chelating agent refers to a substance that has the ability to further improve the desensitization ability of a processing liquid and also to prevent scumming during printing when the processing liquid of the present invention is diluted and used as a dampening liquid. Examples include sodium, potassium, and ammonium salts of ethylenediaminetetraacetic acid, diethylenetriaminepentaacetic acid, iminodiacetic acid, nitrilotriacetic acid, pyrophosphoric acid, triphosphoric acid, etc., and the concentration in the treatment liquid is 0.1 g/~100
g/ is preferable, and a particularly preferable range is 5 g/
~50g/. Furthermore, suitable amounts of inorganic and organic acids and basic substances, as well as known preservatives and rust preventives, can be added as acidity regulators for the treatment liquid. When using the treatment liquid of the present invention, the pH of the liquid is
A range of 3.0 to 6.0 is desirable. Moreover, this treatment liquid can be diluted 4 to 10 times with water and used as a humidifying liquid. Next, the present invention will be explained with reference to Examples and Comparative Examples. Example 1 Potassium dihydrogen phosphate 3.0 g Acidic colloidal silicic acid (particle size 20 mμ) 0.2 g Diammonium citrate 1.0 g Glycerin 4.0 g Water was added to sufficiently dissolve 100 g, and the pH of the solution was adjusted to 4.5. Example 2 Ammonium dihydrogen phosphate 3.0 g Acidic colloidal silicic acid (particle size 20 mμ) 0.2 g Sodium gluconate 1.5 g Glycerin 4.0 g Water was added to sufficiently dissolve 100 g, and the pH of the solution was adjusted to 4.5. Example 3 Calcium dihydrogen phosphate 3.0 g Acidic colloidal silicic acid (particle size 20 mμ) 0.2 g Potassium phthalate 1.0 g Glycerin 4.0 g Water was added to sufficiently dissolve 100 g, and the PHH of the solution was adjusted to 4.5. Comparative Example 1 Inositohexalic acid ester 3.0g Acidic colloidal silicic acid (particle size 20mμ) 0.2g Diammonium citrate 1.0g Glycerin 4.0g Water was added to sufficiently dissolve 100g, and the pH of the solution was adjusted to 4.5. Comparative Example 2 Disodium hydrogen phosphate 3.0 g Acidic colloidal silicic acid (particle size 20 mμ) 0.2 g Sodium gluconate 1.0 g Glycerin 4.0 g Water was added to sufficiently dissolve 100 g, and the pH of the solution was adjusted to 4.5. Comparative Example 3 3.0 g of potassium dihydrogen phosphate, 0.2 g of acidic colloidal silicic acid (particle size 50 mμ), 1.0 g of diammonium citrate, 4.0 g of glycerin, and 91.8 g of distilled water were sufficiently dissolved to adjust the PHH of the solution to 6.1. On the other hand, after forming an image using a commercially available electrophotographic offset master according to a conventional method, etching converter OH-11 (manufactured by Mitsubishi Paper Industries) was used with each processing solution.
A one-time desensitization treatment was carried out at . Further, as the humidifying water, a solution diluted with a volume ratio of 1 part of the same treatment solution to 9 parts tap water was used. The table shows the results of printing with a small offset printing machine (Toko model 8:10, manufactured by Tokyo Aircraft Instruments).

【表】 以上の様に、実施例1〜3では、5000枚印刷し
ても地汚れがなく、また印刷始めのインク乗りも
良好であつたが、比較例1では地汚れは発生しな
かつたものの非常にインク乗りが悪く、また比較
例2及び3では10枚程度で汚れてしまい印刷を経
続することが出来なかつた。
[Table] As shown above, in Examples 1 to 3, there was no background smudge even after printing 5000 sheets, and the ink coverage at the beginning of printing was good, but in Comparative Example 1, no background smear occurred. However, the ink transfer was very poor, and in Comparative Examples 2 and 3, the printing became smeared after about 10 sheets, and printing could not be continued.

Claims (1)

【特許請求の範囲】 1 リン酸二水素塩及びSiOH基を有する粒径40
mμ以下の酸性コロイド硅酸を含有することを特
徴とする平版印刷版用不感脂化処理液。 2 リン酸二水素塩濃度が1.0g/〜300g/
、前記酸性コロイド硅酸濃度が0.1g/〜30
g/である特許請求の範囲第1項記載の平版印
刷版用不感脂化処理液。
[Claims] 1. Particle size 40 containing dihydrogen phosphate and SiOH group
A desensitizing treatment liquid for lithographic printing plates, characterized in that it contains acidic colloidal silicic acid of mμ or less. 2 Dihydrogen phosphate concentration is 1.0g/~300g/
, the acidic colloidal silicic acid concentration is 0.1g/~30
The desensitizing treatment liquid for lithographic printing plates according to claim 1, which is
JP5879885A 1985-03-22 1985-03-22 Desensitizing treatment solution of planographic printing plate Granted JPS61215089A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5879885A JPS61215089A (en) 1985-03-22 1985-03-22 Desensitizing treatment solution of planographic printing plate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5879885A JPS61215089A (en) 1985-03-22 1985-03-22 Desensitizing treatment solution of planographic printing plate

Publications (2)

Publication Number Publication Date
JPS61215089A JPS61215089A (en) 1986-09-24
JPH0517879B2 true JPH0517879B2 (en) 1993-03-10

Family

ID=13094602

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5879885A Granted JPS61215089A (en) 1985-03-22 1985-03-22 Desensitizing treatment solution of planographic printing plate

Country Status (1)

Country Link
JP (1) JPS61215089A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5374168B2 (en) * 2009-01-20 2013-12-25 三菱製紙株式会社 Printing method of heat-sensitive lithographic printing plate
JP5639373B2 (en) * 2010-03-17 2014-12-10 三菱製紙株式会社 Printing method of heat-sensitive lithographic printing plate
JP5639378B2 (en) * 2010-03-31 2014-12-10 三菱製紙株式会社 Printing method of heat-sensitive lithographic printing plate

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5196602A (en) * 1975-02-21 1976-08-25 OFUSETSUTOMASUTAAYOSHORIEKI
JPS58140299A (en) * 1982-02-17 1983-08-19 Fuji Photo Film Co Ltd Treating liquid for making offset master hydrophilic
JPS58215399A (en) * 1982-06-09 1983-12-14 Fuji Photo Film Co Ltd Treatment of offset master for making it hydrophilic
JPS5935994A (en) * 1982-08-24 1984-02-27 Tomoegawa Paper Co Ltd Fat-disaffinity processing liquid for printing
JPS59207290A (en) * 1983-05-12 1984-11-24 Tomoegawa Paper Co Ltd Processing solution insensitive to fat for printing

Also Published As

Publication number Publication date
JPS61215089A (en) 1986-09-24

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