JP2866185B2 - Lithographic printing plate developer - Google Patents

Lithographic printing plate developer

Info

Publication number
JP2866185B2
JP2866185B2 JP28014590A JP28014590A JP2866185B2 JP 2866185 B2 JP2866185 B2 JP 2866185B2 JP 28014590 A JP28014590 A JP 28014590A JP 28014590 A JP28014590 A JP 28014590A JP 2866185 B2 JP2866185 B2 JP 2866185B2
Authority
JP
Japan
Prior art keywords
silver
printing plate
lithographic printing
developer
silver halide
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
JP28014590A
Other languages
Japanese (ja)
Other versions
JPH04155343A (en
Inventor
栄治 松原
偉俊 三浦
滝美 橋本
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 JP28014590A priority Critical patent/JP2866185B2/en
Priority to US07/774,611 priority patent/US5258258A/en
Publication of JPH04155343A publication Critical patent/JPH04155343A/en
Application granted granted Critical
Publication of JP2866185B2 publication Critical patent/JP2866185B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION 【産業上の利用分野】[Industrial applications]

本発明は、銀錯塩拡散転写法による平版印刷版に用い
る現像液に関する。
The present invention relates to a developer used for a lithographic printing plate prepared by a silver complex salt diffusion transfer method.

【従来技術及びその問題点】[Prior art and its problems]

写真的な複製方法の一つである銀錯塩拡散転写法(DT
R法)によって得られる銀画像を、オフセット印刷原版
として用いることができるようにした印刷版は、既に特
公昭46−43132号あるいは特公昭48−30562号に記載され
ており、さらにポジタイプの印刷原版については、特開
昭49−55402号に、ネガタイプの印刷原版については特
開昭52−106902号、特開昭52−112402号等に詳細に記載
されている。 この様な平版印刷版の製版法に適した銀錯塩拡散転写
法の代表的な実施法によれば、支持体およびその上にハ
レーション防止をかねた下引層、ハロゲン化銀乳剤層、
物理現像核層からなる感光材料を像様露光し、現像処理
を行うと潜像が形成されているハロゲン化銀は乳剤層中
で化学現像され黒化銀となる。同時に潜像が形成されて
いないハロゲン化銀は現像処理液中に含まれるハロゲン
化銀錯化剤の作用で溶解し、感光材料の表面に拡散して
くる。溶解し拡散してきた銀錯塩が表面層の物理現像核
の上に現像主薬の還元作用によって銀画像として析出す
る。得られた銀画像のインキ受容性を強化させるために
現像処理に続いて、必要ならば感脂化処理が施された
後、オフセット印刷機にセットされ、印刷物へとインキ
画像が転写される。 この印刷版に必要となる諸性能は、印刷材料に依存す
ると同時にそれを製版する工程、とりわけ現像処理工程
に強く依存している。即ち、拡散転写により生じた銀画
像の性質が印刷特性に与える影響は大きい。例えば、転
写銀粒子の生成条件、たとえば銀錯塩の拡散速度と安定
度あるいは還元速度が重要な因子となり、又、米国特許
第4,297,429号、同第4,297,403号、同第4,355,090号明
細書には、転写銀粒子の生成条件にハロゲン化銀溶剤の
種類が重要な影響を及ぼすことが示されている。しか
し、未だ銀錯化剤として十分満足出来るものはなかっ
た。
Silver complex salt diffusion transfer method (DT
R)), a printing plate capable of using a silver image as an offset printing plate has already been described in JP-B-46-43132 or JP-B-48-30562. Are described in detail in JP-A-49-55402, and negative-type printing original plates are described in JP-A-52-106902 and JP-A-52-112402. According to a typical implementation method of the silver complex salt diffusion transfer method suitable for the plate making method of such a lithographic printing plate, a support and an undercoat layer which also prevents halation thereon, a silver halide emulsion layer,
When the photosensitive material comprising the physical development nucleus layer is imagewise exposed and developed, the silver halide on which the latent image is formed is chemically developed in the emulsion layer to become blackened silver. At the same time, the silver halide having no latent image formed thereon is dissolved by the action of the silver halide complexing agent contained in the developing solution and diffuses to the surface of the photosensitive material. The dissolved and diffused silver complex is deposited as a silver image on the physical development nuclei of the surface layer by the reducing action of the developing agent. After the development process for enhancing the ink receptivity of the obtained silver image and, if necessary, a sensitization process, if necessary, the silver image is set on an offset printing machine, and the ink image is transferred to a print. The various properties required for the printing plate depend not only on the printing material but also on the process of making the plate, especially on the development process. That is, the properties of the silver image generated by the diffusion transfer greatly affect the printing characteristics. For example, transfer silver particle formation conditions, such as the diffusion rate and stability or reduction rate of the silver complex are important factors, and U.S. Pat.Nos. 4,297,429, 4,297,403, and 4,355,090 describe the transfer. It has been shown that the type of silver halide solvent has a significant effect on the silver grain formation conditions. However, none of the silver complexing agents has been sufficiently satisfactory.

【発明の目的】 本発明は、銀錯塩拡散転写法を使った平版印刷版用処
理液に関するものであり、特に耐刷性の優れた印刷版を
得るための処理液を提供するものである。
The present invention relates to a processing solution for a lithographic printing plate using a silver complex salt diffusion transfer method, and more particularly to a processing solution for obtaining a printing plate having excellent printing durability.

【発明の構成】Configuration of the Invention

本発明の目的は、銀錯塩拡散転写法を利用する平版印
刷版に於て、ハロゲン化銀溶剤として一般式(I)で示
されるチオエーテル誘導体を含有する処理液を使うこと
により達成された。 一般式(I) X−SR1−SnR2−S−X 式中Xはカルボキシ基を有する芳香族基、(好ましく
はアリール基)、複素環基(ピリジン環、チエゾール
環、オキサゾール環、イミダゾール環など)を表わし、
R1、R2はアルキレン基(好ましくはエチレン、プロピレ
ン、テトラメチレン)を表わし、nは0、1、2又は3
を表わす。 本発明に用いられるチオエーテル誘導体の代表的な具
体例を以下に示す。 本発明のチオエーテル類の合成は基本的には、相当す
るチオールのアルキル化により行なった。アルキル化剤
は例えばジャーナル.オブ・オルガニック・ケミストリ
ー(J.O.C.)26、4897(1961)の方法で容易に合成でき
る。以下に合成例を用いて合成方法の詳細を述べる。 合成例1(例示化合物2の合成) チオサリチル酸1.5gをエタノール30mlに溶解し、トリ
エチルアミン1.1gを加え、続いて3,6−ジチア−1,8−オ
クタンジクロライド1.2gを加える。還流3時間。析出物
濾取、水洗、乾燥後、メチルアルコールより再結晶し、
白色粉末を得た。 mp228〜230℃ 収量1.8g CMR(DMSO) δ167.2、139.5、131.9、130.6、128.8、
125.6、123.9、31.5、29.9 本発明のチオエーテル誘導体を現像液に含有させる量
は約5〜50g/lであり、好ましくは約10〜約30g/lの範囲
がよい。 本発明の現像処理液には、アルカリ性物質、例えば水
酸化ナトリウム、水酸化カリウム、水酸化リチウム、第
三燐酸ナトリウム等、保恒剤としての亜硫酸塩、ハロゲ
ン化銀溶剤、例えばチオ硫酸塩、チオシアン酸塩、環状
イミド、チオサリチル酸、アミン等、粘稠剤、例えばヒ
ドロキシエチルセルロース、カルボキシメチルセルロー
ス、かぶり防止剤、例えば臭化カリウム、1−フェニル
−5−メルカプトテトラゾール、特開昭47−26201に記
載の化合物、現像剤、例えばハイドロキノン、1−フェ
ニル−3−ピラゾリドン、現像変性剤、例えばポリオキ
シアルキレン化合物、オニウム化合物等を含むことがで
きる。 銀錯塩拡散転写法を実施するに当っては、例えば英国
特許第1,000,115号、第1,012,476号、第1,017,273号、
第1,042,477号等の明細書に記載されている如く、ハロ
ゲン化銀乳剤層および/または受像層またはそれに隣接
する他の水透過性層中に現像剤を混入することが行われ
ている。従って、このような材料に於いては、現像段階
で使用される処理液は、現像剤を含まぬ所謂「アルカリ
性活性化液」を使用しうる。 本発明の実施に用いられる平版印刷版のハロゲン化銀
乳剤は塩化銀、臭化銀、塩臭化銀、塩ヨウ化銀、塩臭ヨ
ウ化銀等が使用でき、好ましくは塩化銀が50モル%以上
のハロゲン化銀である。これらのハロゲン化銀乳剤は分
光増感剤(光源、用途に応じた分光増感色素。例えばカ
メラタイプ、レーザー光タイプ、色分解用パンクロタイ
プなど)、ゼラチン硬化剤、塗布助剤、カブリ防止剤、
可塑剤、現像剤、マット剤などを含むことができる。 ハロゲン化銀乳剤の結合剤は、一般にこの目的に使用
される天然及び、又は合成結合剤、例えばゼラチン、コ
ロイド状アルブミン、セルロース誘導体等が使用出来
る。 ハロケン化銀乳剤層の下側(支持体面)には接着改良
用下引層及び又はハレーション防止等の目的で下塗層を
含むことも出来、この層には現像剤、マット剤を含むこ
ともできる。 ハロゲン化銀乳剤を塗布する支持体は、紙、各種のフ
ィルム、プラスチックス、樹脂様物質を塗布した紙、金
属等が使用できる。 物理現像核層に使用される物理現像核は、この種の薬
品の例は周知であって、アンチモン、ビスマス、カドミ
ウム、コバルト、パラジウム、ニッケル、銀、鉛、亜鉛
などの金属およびその硫化物が使用できる。この物理現
像核層にも現像剤を含むことができるし、親水性バイン
ダーを含んでもよい。 本発明により製造された平版印刷版は、例えば特公昭
48−29723、米国特許第3,721,539号等明細書に記載され
ている如き化合物でインキ受理性に変換ないし増強しう
る。 印刷方法あるいは使用する不感脂化液、給湿液などは
普通によく知られた方法によることができる。
The object of the present invention has been achieved by using a processing solution containing a thioether derivative represented by the general formula (I) as a silver halide solvent in a lithographic printing plate utilizing a silver complex salt diffusion transfer method. General formula (I) X-SR 1 -S n R 2 -S-X wherein X is an aromatic group having a carboxyl group, (preferably an aryl group), a Hajime Tamaki (pyridine ring, Chiezoru ring, oxazole ring, Represents an imidazole ring),
R 1 and R 2 represent an alkylene group (preferably ethylene, propylene, tetramethylene), and n is 0, 1, 2, or 3
Represents Representative specific examples of the thioether derivative used in the present invention are shown below. The synthesis of the thioethers according to the invention was basically carried out by alkylation of the corresponding thiols. Alkylating agents are described, for example, in Journal. It can be easily synthesized by the method of Organic Chemistry (JOC) 26 , 4897 (1961). The details of the synthesis method are described below using synthesis examples. Synthesis Example 1 (Synthesis of Exemplified Compound 2) 1.5 g of thiosalicylic acid was dissolved in 30 ml of ethanol, and 1.1 g of triethylamine was added, followed by 1.2 g of 3,6-dithia-1,8-octane dichloride. 3 hours at reflux. The precipitate was collected by filtration, washed with water, dried, and recrystallized from methyl alcohol.
A white powder was obtained. mp228-230 ° C Yield 1.8 g CMR (DMSO) δ 167.2, 139.5, 131.9, 130.6, 128.8,
125.6, 123.9, 31.5, 29.9 The amount of the thioether derivative of the present invention contained in the developer is about 5 to 50 g / l, preferably about 10 to about 30 g / l. In the developing solution of the present invention, an alkaline substance such as sodium hydroxide, potassium hydroxide, lithium hydroxide, sodium tertiary phosphate and the like, a sulfite as a preservative, a silver halide solvent such as thiosulfate, thiocyanate Acid salts, cyclic imides, thiosalicylic acid, amines, etc., thickeners such as hydroxyethyl cellulose, carboxymethyl cellulose, antifoggants such as potassium bromide, 1-phenyl-5-mercaptotetrazole, described in JP-A-47-26201. Compounds and developers such as hydroquinone, 1-phenyl-3-pyrazolidone, and development modifiers such as polyoxyalkylene compounds and onium compounds can be included. In carrying out the silver complex salt diffusion transfer method, for example, British Patent No. 1,000,115, No. 1,012,476, No. 1,017,273,
As described in the specification of Japanese Patent No. 1,042,477 and the like, a developer is mixed in a silver halide emulsion layer and / or an image receiving layer or another water-permeable layer adjacent thereto. Therefore, in such a material, a so-called “alkaline activating liquid” containing no developer can be used as a processing liquid used in the developing step. The silver halide emulsion of the lithographic printing plate used in the practice of the present invention can be silver chloride, silver bromide, silver chlorobromide, silver chloroiodide, silver chlorobromoiodide, etc., preferably 50 mol of silver chloride. % Or more of silver halide. These silver halide emulsions are spectral sensitizers (spectral sensitizing dyes according to the light source and application, for example, camera type, laser light type, panchromatic type for color separation, etc.), gelatin hardener, coating aid, antifoggant ,
It may contain a plasticizer, a developer, a matting agent and the like. As the binder for the silver halide emulsion, natural and / or synthetic binders generally used for this purpose, for example, gelatin, colloidal albumin, cellulose derivatives and the like can be used. Under the silver halogenated emulsion layer (the surface of the support), an undercoat layer for improving adhesion and / or an undercoat layer for the purpose of preventing halation may be included. This layer may include a developer and a matting agent. it can. As the support on which the silver halide emulsion is coated, paper, various films, plastics, paper coated with a resin-like substance, metal and the like can be used. Physical development nuclei used in the physical development nucleus layer are well-known examples of this kind of chemicals, and include metals such as antimony, bismuth, cadmium, cobalt, palladium, nickel, silver, lead, zinc, and sulfides thereof. Can be used. This physical development nucleus layer may also contain a developer, and may also contain a hydrophilic binder. The lithographic printing plate manufactured according to the present invention is described in, for example,
Compounds such as those described in U.S. Pat. No. 3,721,539, et al., Can convert or enhance ink acceptance. The printing method, the desensitizing solution, the humidifying solution, and the like to be used can be a commonly known method.

【実施例】【Example】

以下に本発明を実施例により具体的に説明するが、勿
論、これだけに限定されるものではない。 実施例1 下引処理したポリエステルフィルム支持体の片面に平
均粒子サイズ5μのシリカ粒子を含有するマット化層を
設け、反対側の面に633nmの光反射率が3%になる量の
カーボンブラックを含み、写真用ゼラチンに対して20重
量%の平均粒径7μmのシリカ粉末を含むハレージン防
止用下塗層(pH4.0に調整)と、化学増感された後に平
均粒7μmのシリカ粉末を写真用ゼラチンに対して5重
量%の割合で含むスペクトル増感された高感度塩化銀乳
剤(pH4.0に調整)とを設けた。 下塗層のゼラチンは3.5g/m2、乳剤層のゼラチンは0.8
g/m2、硝酸銀に換算したハロゲン化銀1.0g/m2の割合で
塗布された。この下塗層と乳剤層は硬化剤としてホルマ
リンをゼラチンに対して5.0mg/gゼラチンの量で含んで
いる。乾燥後40℃で14日間加温した後、この乳剤層の上
に、特開昭54−103104実施例2のプレートNo.31記載の
核塗液を塗布、乾燥し、平版印刷版を製造する。ハロゲ
ン化銀乳剤は、物理熟成時にハロゲン化銀1モル当り4
×10-6モルの塩化ロジウムを点火したものであり、平均
粒径0.40ミクロンであった。 このようにして得られた平版印刷版の原版に像反転機
構を有する製板カメラで像露光し、下記の現像液A(使
用液)により30℃で30秒間現像処理し、続いて下記中和
液で処理した。 一方、前記の比較現像液Aの2−メチル−2−アミノ
−1−プロパノールの代わりに例示の化合物(2)を10
g含有させた現像液Bを用いる以外は全く同様にして製
板処理した。他に比較化合物として、3,6−ジチア−1,8
−オクタンジオールを使用した。(現像液C) 以上の操作により作製した印刷版をオフセット印刷機
にセットし、下記組成のエッチ液を版面にくまなく与
え、下記組成の給湿液を用いて印刷を行った。 印刷機はエー・ビー・ディック350CD(A・B・Dick
社製オフセット印刷機の商標)を使用した。 現像液A、Cで得られた印刷版は、5000枚までに転写
銀像の部分的な欠落が生じたのに対して、本発明の現像
液Bで得られた印刷版は、10,000枚でも転写銀像の欠落
は生じなかった。又、インキ乗り性はいずれも差がなか
った。 実施例2 実施例1の比較現像液Aの2−メチル−2−アミノ−
1−プロパノールの代わりに例示の化合物(1)及び
(4)を各々20g含有させた現像液を用いる以外は実施
例1に従った。いずれも10,000枚の印刷で転写銀像の欠
落は生じなかった。 実施例3 下記の現像液に例示の化合物(1)、(2)、
(3)、(5)、(7)、(8)を各々15g含有させ実
施例1に準じて試験した。実施例1、2と同様に優れた
効果のあることが確認された。 (F)発明の効果 本発明の現像液で製版された平版印刷版は、転写銀像
の欠落が改良され、大きな耐刷力の向上が図れ、インキ
乗り性も低下しない。
Hereinafter, the present invention will be described specifically with reference to Examples, but it is needless to say that the present invention is not limited thereto. Example 1 A matted layer containing silica particles having an average particle size of 5 μm was provided on one surface of a polyester film support subjected to an undercoating treatment, and the opposite surface was coated with an amount of carbon black having an optical reflectance of 633 nm of 3%. A photographic gelatin containing 20% by weight of silica powder with an average particle size of 7 μm based on photographic gelatin, and an undercoat layer for anti-halazin (adjusted to pH 4.0), and a silica powder with an average particle size of 7 μm after chemical sensitization. And a spectrally sensitized silver chloride emulsion (adjusted to pH 4.0) containing 5% by weight of gelatin for use. The gelatin of the undercoat layer is 3.5 g / m 2 , and the gelatin of the emulsion layer is 0.8
g / m 2 , and silver halide was converted at a rate of 1.0 g / m 2 in terms of silver nitrate. The undercoat layer and the emulsion layer contain formalin as a hardener in an amount of 5.0 mg / g gelatin relative to gelatin. After heating at 40 ° C. for 14 days after drying, a nucleus coating solution described in Plate No. 31 of Example 2 of JP-A-54-103104 was applied on this emulsion layer and dried to produce a lithographic printing plate. . The silver halide emulsion was added at 4 times per mole of silver halide during physical ripening.
It was ignited with × 10 -6 moles of rhodium chloride and had an average particle size of 0.40 microns. The thus obtained lithographic printing plate precursor was image-exposed with a plate making camera having an image reversing mechanism, developed with the following developer A (used solution) at 30 ° C. for 30 seconds, and then neutralized as follows. The solution was treated. On the other hand, in place of 2-methyl-2-amino-1-propanol of the comparative developer A, the exemplified compound (2) was
A plate-making process was performed in exactly the same manner except that the developer B containing g was used. Other comparative compounds include 3,6-dithia-1,8
-Octanediol was used. (Developer C) The printing plate prepared by the above operation was set in an offset printing machine, an etchant having the following composition was applied all over the plate surface, and printing was performed using a humidifying solution having the following composition. The printing machine is AB Dick 350CD (AB Dick)
(Trademark of an offset printing machine manufactured by KK). In the printing plates obtained with the developing solutions A and C, a partial loss of the transferred silver image occurred up to 5,000 sheets, whereas the printing plate obtained with the developing solution B of the present invention showed 10,000 sheets. No loss of the transferred silver image occurred. In addition, there was no difference in ink ridability. Example 2 2-Methyl-2-amino- of Comparative Developer A of Example 1
Example 1 was followed except that a developer containing 20 g of each of the exemplified compounds (1) and (4) was used instead of 1-propanol. In each case, no loss of the transferred silver image occurred after printing 10,000 sheets. Example 3 Examples of the compounds (1), (2),
(3), (5), (7), and (8) were each contained in 15 g and tested according to Example 1. It was confirmed that excellent effects were obtained as in Examples 1 and 2. (F) Effects of the Invention In the lithographic printing plate made with the developing solution of the present invention, the loss of the transferred silver image is improved, the printing durability is largely improved, and the ink running property is not reduced.

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Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】銀錯塩拡散転写法を利用する平版印刷版の
現像液に於て、下記一般式(I)のチオエーテル誘導体
を含有することを特徴とする平版印刷版用現像液。 一般式(I) X−SR1−SnR2−S−X (式中Xはカルボキシ基を有する芳香族基、複素環基を
表わし、R1、R2はアルキレン基を表わし、nは0、1、
2又は3を表わす。)
1. A lithographic printing plate developer using a silver complex salt diffusion transfer method, comprising a thioether derivative represented by the following general formula (I): Formula (I) X—SR 1 —S n R 2 —SX (wherein X represents an aromatic group or a heterocyclic group having a carboxy group, R 1 and R 2 represent an alkylene group, and n represents 0, 1,
Represents 2 or 3. )
JP28014590A 1990-10-11 1990-10-18 Lithographic printing plate developer Expired - Lifetime JP2866185B2 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP28014590A JP2866185B2 (en) 1990-10-18 1990-10-18 Lithographic printing plate developer
US07/774,611 US5258258A (en) 1990-10-11 1991-10-10 Process for making lithographic printing plates

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP28014590A JP2866185B2 (en) 1990-10-18 1990-10-18 Lithographic printing plate developer

Publications (2)

Publication Number Publication Date
JPH04155343A JPH04155343A (en) 1992-05-28
JP2866185B2 true JP2866185B2 (en) 1999-03-08

Family

ID=17620956

Family Applications (1)

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Country Link
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Also Published As

Publication number Publication date
JPH04155343A (en) 1992-05-28

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