JPH04306660A - Processing for lithographic form plate - Google Patents
Processing for lithographic form plateInfo
- Publication number
- JPH04306660A JPH04306660A JP9957391A JP9957391A JPH04306660A JP H04306660 A JPH04306660 A JP H04306660A JP 9957391 A JP9957391 A JP 9957391A JP 9957391 A JP9957391 A JP 9957391A JP H04306660 A JPH04306660 A JP H04306660A
- Authority
- JP
- Japan
- Prior art keywords
- lithographic printing
- silver
- supporting body
- development
- sodium thiosulfate
- 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.)
- Granted
Links
- 238000007639 printing Methods 0.000 claims abstract description 46
- 229910052709 silver Inorganic materials 0.000 claims abstract description 23
- 239000004332 silver Substances 0.000 claims abstract description 23
- -1 silver halide Chemical class 0.000 claims abstract description 17
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 15
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 15
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims abstract description 12
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 claims abstract description 12
- 235000019345 sodium thiosulphate Nutrition 0.000 claims abstract description 12
- 239000000839 emulsion Substances 0.000 claims abstract description 11
- 238000009792 diffusion process Methods 0.000 claims abstract description 7
- 238000000034 method Methods 0.000 claims description 16
- 238000011282 treatment Methods 0.000 abstract description 17
- 239000000084 colloidal system Substances 0.000 abstract description 7
- 238000007788 roughening Methods 0.000 abstract description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 abstract description 4
- 150000001875 compounds Chemical class 0.000 abstract description 4
- 230000003647 oxidation Effects 0.000 abstract description 4
- 238000007254 oxidation reaction Methods 0.000 abstract description 4
- 239000007788 liquid Substances 0.000 abstract description 3
- 150000003839 salts Chemical class 0.000 abstract description 3
- 239000000126 substance Substances 0.000 abstract description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 abstract description 2
- 229910052737 gold Inorganic materials 0.000 abstract description 2
- 239000010931 gold Substances 0.000 abstract description 2
- 229910052976 metal sulfide Inorganic materials 0.000 abstract description 2
- 229910052763 palladium Inorganic materials 0.000 abstract description 2
- NDGRWYRVNANFNB-UHFFFAOYSA-N pyrazolidin-3-one Chemical compound O=C1CCNN1 NDGRWYRVNANFNB-UHFFFAOYSA-N 0.000 abstract description 2
- 229910052725 zinc Inorganic materials 0.000 abstract description 2
- 239000011701 zinc Substances 0.000 abstract description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- 239000004411 aluminium Substances 0.000 abstract 2
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 abstract 1
- 108010010803 Gelatin Proteins 0.000 description 12
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 12
- 229920000159 gelatin Polymers 0.000 description 12
- 235000019322 gelatine Nutrition 0.000 description 12
- 235000011852 gelatine desserts Nutrition 0.000 description 12
- 239000008273 gelatin Substances 0.000 description 11
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 239000000243 solution Substances 0.000 description 7
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- JKFYKCYQEWQPTM-UHFFFAOYSA-N 2-azaniumyl-2-(4-fluorophenyl)acetate Chemical group OC(=O)C(N)C1=CC=C(F)C=C1 JKFYKCYQEWQPTM-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 229910021607 Silver chloride Inorganic materials 0.000 description 2
- 229910021612 Silver iodide Inorganic materials 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 229920001477 hydrophilic polymer Polymers 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 2
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
- 229940045105 silver iodide Drugs 0.000 description 2
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 2
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- JAAIPIWKKXCNOC-UHFFFAOYSA-N 1h-tetrazol-1-ium-5-thiolate Chemical compound SC1=NN=NN1 JAAIPIWKKXCNOC-UHFFFAOYSA-N 0.000 description 1
- 102000009027 Albumins Human genes 0.000 description 1
- 108010088751 Albumins Proteins 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 241000978776 Senegalia senegal Species 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 1
- XCFIVNQHHFZRNR-UHFFFAOYSA-N [Ag].Cl[IH]Br Chemical compound [Ag].Cl[IH]Br XCFIVNQHHFZRNR-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000002048 anodisation reaction Methods 0.000 description 1
- 238000007743 anodising Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 238000007645 offset printing Methods 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 1
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 1
- 229910001961 silver nitrate Inorganic materials 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Abstract
Description
【発明の詳細な説明】
【0001】
【産業上の利用分野】本発明は、印刷性を改良した平版
印刷版の処理方法に関するものである。
【0002】
【従来の技術】銀錯塩拡散転写法(DTR法)を用いた
平版印刷版については、フォーカル・プレス、ロンドン
・ニューヨーク(1972年)発行、アンドレ・ロット
及びエディス・ワイデ著、「フォトグラフィック・シル
バー・ハライド・ディヒュージョン・プロセシズ」、第
101頁〜第130頁に幾つかの例が記載されている。
【0003】その中で述べられているように、DTR法
を用いた平版印刷版には、転写材料と受像材料を別々に
したツーシートタイプ、あるいはそれらを一枚の支持体
上に設けたモノシートタイプの二方式が知られている。
ツーシートタイプの平版印刷版については、特開昭57
ー158844号明細書に詳しく記載されている。又、
モノシートタイプについては、特公昭48ー30562
号、同51ー15765号、特開昭51ー111103
号、同52ー150105号などの各明細書に詳しく記
載されている。
【0004】紙を支持体とした平版印刷版は、印刷中の
版伸びや水分のしみ込みなどのため耐刷性を含め高品質
の印刷は困難である。これらの問題点を改良し印刷性能
を向上する目的でフィルム支持体が用いられる。例えば
、酢酸セルロースフィルム、ポリビニルアセタールフィ
ルム、ポリスチレンフィルム、ポリプロピレンフィルム
、ポリエチレンテレフタレートフィルム、或はポリエス
テル、ポリプロピレン、又はポリスチレンフィルムなど
をポリエチレンフィルムで被覆した複合フィルム等が支
持体として利用できる。
【0005】しかしながら、フィルムを支持体とした平
版印刷版は紙ベースの印刷版と比べ、版伸び性や水分の
しみ込みなどの点で改良されたものの、耐刷性、保水性
、更には印刷機への版掛け性等の点で問題を残している
。
【0006】そこで、上に述べた紙やフィルムを支持体
とした平版印刷版の種々の問題点を解決するために、金
属特にアルミニウムを支持体とした銀塩方式の平版印刷
版が知られており、特開昭57ー118244号、同5
7ー158844号、同63ー260491号などの各
明細書に詳しく記載されている。
【0007】特開昭63ー260491号明細書では、
アルミニウムを支持体とし、その上に物理現像核層を設
け、更にその上に感光性ハロゲン化銀乳剤層を設けたモ
ノシートタイプの、DTR法を利用した平版印刷版が詳
述されている。それによれば、上記平版印刷版を像露光
し、拡散転写現像した後、残留乳剤被膜を温水中で洗浄
して除去し印刷版を作製する。
【0008】
【発明が解決しようとする課題】本発明者等は、上記特
許に記載されたアルミニウムを支持体とするモノシート
タイプでDTR方式の平版印刷版において、その処理方
法を種々検討し次の問題点を見いだした。即ち、該平版
印刷版を、特開昭57ー158844号や同63ー26
0491号明細書の実施例に記載されている様な現像液
を用いて現像を行なっても、インキ乗りが遅く、十分な
耐刷力が得られないという問題があることが分かった。
【0009】本発明の目的は、上記問題を解決し、イン
キ乗り、耐刷力の改善された平版印刷版を提供すること
である。
【0010】
【課題を解決するための手段】本発明の上記目的は、支
持体として陽極酸化されたアルミニウムを用い、その上
に物理現像核層及び感光性ハロゲン化銀写真乳剤層を有
する平版印刷版において、1l当たりのチオ硫酸ナトリ
ウムの含有量が2gを越えない処理液で現像することに
よって達成された。
【0011】本発明の平版印刷版に用いられるアルミニ
ウム支持体は、その上に設けられる感光層との密着性を
向上し、且つ保水性を改善するため、その表面を粗面化
することが行われる。この粗面化処理(いわゆるグレイ
ニング)には、ボールグレイニング、ワイヤグレイニン
グ、ブラシグレイニング等の機械的粗面化処理、塩化物
、フッ化物等で化学的にアルミニウムを溶解することに
より行う化学的粗面化処理、及び電気化学的にアルミニ
ウムを溶解することにより行う電解粗面化処理がある。
【0012】粗面化処理を行なった後、陽極酸化処理を
行なう必要がある。陽極酸化処理は、従来よりよく知ら
れている方法を用いることが出来るが、硫酸が最も有用
な電解液として用いられる。それについで、リン酸、硝
酸なども有用な電解液である。さらに特開昭55ー28
400号明細書に開示されている硫酸とリン酸の混合液
もまた有用である。
【0013】硫酸法は、通常直流電流で処理が行われる
が、交流を用いることも可能である。硫酸の濃度は5〜
30%で使用され、20〜60℃の温度範囲で5〜25
0秒間電解処理されて、表面に1〜10g/m2の酸化
被膜が設けられる。さらにこのときの電流密度は1〜2
0A/dm2が好ましい。リン酸法の場合には、5〜5
0%の濃度、30〜60℃の温度で、10〜300秒間
、1〜15A/dm2の電流密度で処理される。
【0014】尚、陽極酸化処理に先立ってデスマット処
理を施すことが好ましい。すなわち、粗面化処理したア
ルミニウム基板を、10〜50%の熱硫酸(40〜60
℃)や希薄なアルカリ(水酸化ナトリウム等)で処理す
ることにより表面に付着したスマットが除去される。
【0015】また、陽極酸化処理を行なった後、必要に
応じて後処理を行うことが出来る。例えば、英国特許第
1,230,447号に開示されたポリビニルホスホン
酸の水溶液中に浸漬処理する方法が用いられる。また、
必要に応じて、親水性高分子の下塗層を設けることも可
能であるが、その上に設ける感光層の性質により取捨選
択される。
【0016】本発明で用いられる物理現像核層の物理現
像核として公知の銀錯塩拡散転写法に用いられるもので
よく、例えば金、銀等のコロイド、パラジウム、亜鉛等
の水溶性塩と硫化物を混合した金属硫化物などが使用で
きる。これらの詳細及び製法については、例えば、フォ
ーカル・プレス、ロンドン・ニューヨーク(1972年
)発行、アンドレ・ロット及びエディス・ワイデ著、「
フォトグラフィック・シルバー・ハライド・ディヒュー
ジョン・プロセシズ」を参照し得る。
【0017】本発明の印刷版の感光性ハロゲン化銀乳剤
層には保護コロイドとして各種親水性コロイドを用いる
ことができる。即ち、酸処理ゼラチン、アルカリ処理ゼ
ラチン、ゼラチン誘導体、グラフト化ゼラチン等各種ゼ
ラチンを用いることが出来る他、ポリビニルピロリドン
、各種でんぷん、アルブミン、ポリビニルアルコール、
アラビアゴム、ヒドロキシエチルセルロース、等の親水
性高分子化合物を含有させることが出来る。用いられる
親水性コロイドとしては、ゼラチン、ゼラチン誘導体、
ポリビニルアルコール、ポリビニルピロリドン等が挙げ
られるが、好ましくは、物理現像後の親水性コロイド層
の剥離性を容易にするために実質的に硬膜剤を含まない
親水性コロイド層を用いることが望ましい。
【0018】本発明に用いられる感光性ハロゲン化銀乳
剤の種類としては、一般に用いられる塩化銀、臭化銀、
ヨウ化銀、塩臭化銀、塩ヨウ臭化銀、ヨウ臭化銀等から
選択される。また乳剤のタイプとしてはネガ型、ポジ型
のいずれでもよく、また感光性ハロゲン化銀と難溶化し
た非感光性ハロゲン化銀を用いた特開昭54−4854
4号に記載の特殊なタイプであってもよい。これらのハ
ロゲン化銀乳剤は必要に応じて化学増感あるいはスペク
トル増感することが出来る。
【0019】本発明に用いられる現像主薬としては、ポ
リヒドロキシベンゼン類、3−ピラゾリジノン類が好ま
しく、これらの主薬は版材構成層中に含むいわゆる主薬
内蔵型の形態で用いられてもよい。
【0020】本発明で用いられる現像液には、アルカリ
性物質、例えば水酸化カリウム、水酸化ナトリウム、水
酸化リチウム、第3燐酸ナトリウム、あるいはアミン化
合物、保恒剤 、例えば亜硫酸ナトリウム、粘稠剤、
例えばカルボキシメチルセスロース、カブリ防止剤、例
えば臭化カリウム、色調剤、例えば1−フェニル−5−
メルカプトテトラゾール、現像変成剤、例えばポリオキ
シアルキレン化合物等の添加剤等を含ませることが出来
る。
【0021】現像液のpHとして通常約10〜14、好
ましくは約12〜14であるが、使用する平版印刷版の
アルミニウム支持体の前処理(例えば陽極酸化)条件、
写真要素、所望の像、現像液中の各種化合物の種類及び
量、現像条件等によって異なる。
【0022】ゼラチン層を除去するためのウォッシュオ
フは、温度20〜30℃程度の流水で洗い流す事によっ
て行なうことが出来る。
【0023】
【実施例】
【0024】実施例1
厚さ0.30mmのアルミニウム板を、4%の水酸化ナ
トリウム水溶液で脱脂処理した後、約1%の塩酸溶液中
で10Vの交流を約20分間流した後、直ちに20重量
%の硫酸で1A/dm2の電流密度で5分間陽極酸化を
行ない、さらに水洗乾燥し、表面の陽極酸化されたアル
ミニウム板を調整した。この支持体上に下記の物理現像
核液を銀重量で10 mg/m2の塗布量となるように
塗布した。物理現像核はカレー・レー(Carey L
ea)法により作成された銀ゾルにゼラチン溶液を加え
て、銀とゼラチンの重量比が1となるように調整した。
塗布量は50mg/m2。
【0025】さらに乾燥後下記の構成の感光性ハロゲン
化銀乳剤層を塗布乾燥し感光性平版印刷版を作成した。
オルソ増感された塩化銀乳剤(ヨウ化銀を1モル%含む
。平均粒子サイズ0.3μ)で、硝酸銀で表したハロゲ
ン化銀被覆量2g/m2、ゼラチン塗布量0.4g/m
2。
【0026】このようにして得られた平版印刷板を、ネ
ガフィルムから密着露光計を用いて像露光を行った後、
表1に示すような本発明のチオ硫酸ナトリウムを実質的
に含まない現像液及び、比較現像液としてチオ硫酸ナト
リウムを含む現像液で20℃10秒間現像を行なった後
、直ちに流水で30秒間水洗してゼラチン層を洗い流し
(ウォッシュオフ)した。この様にして得られた感光性
印刷版の画像部の濃度を反射濃度計を用いて測定した。
【0027】
【表1】
【0028】表1から分かるように、本発明の1l当た
りのチオ硫酸ナトリウムの含有量が2gを越えない現像
液を用いて得られた画像銀の濃度は、チオ硫酸ナトリウ
ムを添加することにより著しい低下を示し、1l当たり
のチオ硫酸ナトリウムの含有量が2gを越えると転写銀
量が著しく低下し、チオ硫酸ナトリウムの現像液中での
添加量が8g/lでは、ほとんど転写銀画像を得ること
が出来ないことが分かる。
【0029】実施例2
実施例1の方法で現像した本発明の平版印刷版をウォッ
シュオフ処理した後、版面が乾かないうちに下記の表2
の版面保護液を脱脂綿等で塗布し乾燥させる。この様に
して作成した平版印刷板を、印刷機エー・ビー・ディッ
ク350CD(A.B.Dick社製オフセット印刷機
の商標)にかけ、インキ受理性及び耐刷力を次の方法で
評価した結果を表3に示す。
【0030】
【表2】
【0031】
【表3】
【0032】インキ受理性は版面にインキローラを接触
させながら同時に紙送りを始め、良好な画像濃度の印刷
物が得られるまでの印刷枚数で評価した。耐刷力は画像
部のインキ乗りの不良、あるいは線飛びが生じる時のい
ずれかにより印刷が不可能となったときの印刷枚数で評
価した。
【0033】表3の結果から分かるように、本発明の1
l当たりのチオ硫酸ナトリウムの含有量が2gを越えな
い現像液で処理された平版印刷版はインキ乗りは良好で
かつ極めて高い耐刷性能を有しているのに対し、1l当
たりのチオ硫酸ナトリウムの含有量が2gを越えない現
像液で処理した平版印刷版はインキ乗りが著しく低下し
、また耐刷力もチオ硫酸ナトリウムの添加量が増えるに
したがって著しく低下していることが分かる。
【0034】
【発明の効果】インキ乗りが良好でかつ極めて高い耐刷
性能を有する平版印刷版を得る事ができる。Description: TECHNICAL FIELD The present invention relates to a method for processing lithographic printing plates with improved printability. [0002] Lithographic printing plates using the silver complex diffusion transfer method (DTR method) are described in "Photo" by Andre Lott and Edith Weide, published by Focal Press, London and New York (1972). Some examples are described in "Graphic Silver Halide Diffusion Processes", pages 101-130. As stated therein, lithographic printing plates using the DTR method include a two-sheet type in which the transfer material and image-receiving material are separate, or a two-sheet type in which the transfer material and image-receiving material are separate, or a plate in which they are provided on a single support. Two sheet types are known. Regarding the two-sheet type lithographic printing plate, JP-A-57
It is described in detail in the specification of No.-158844. or,
For the mono sheet type, please refer to Special Publication No. 48-30562.
No. 51-15765, JP-A-51-111103
No. 52-150105 and other specifications. [0004] With lithographic printing plates using paper as a support, it is difficult to print with high quality, including printing durability, due to plate elongation and water penetration during printing. Film supports are used to overcome these problems and improve printing performance. For example, cellulose acetate film, polyvinyl acetal film, polystyrene film, polypropylene film, polyethylene terephthalate film, or a composite film in which polyester, polypropylene, or polystyrene film is coated with polyethylene film, etc. can be used as the support. However, although lithographic printing plates using film as a support have been improved in terms of plate elongation and moisture absorption compared to paper-based printing plates, printing durability, water retention, and even printing Problems remain in terms of ease of applying the plate to the machine, etc. In order to solve the various problems of the above-mentioned lithographic printing plates using paper or film as a support, a silver salt type lithographic printing plate using a metal, especially aluminum, as a support is known. JP-A No. 57-118244, No. 5
It is described in detail in various specifications such as No. 7-158844 and No. 63-260491. [0007] In the specification of JP-A-63-260491,
A monosheet-type lithographic printing plate using the DTR method is described in detail, in which aluminum is used as a support, a physical development nucleus layer is provided thereon, and a photosensitive silver halide emulsion layer is further provided thereon. According to this, after the lithographic printing plate is imagewise exposed and subjected to diffusion transfer development, the residual emulsion coating is removed by washing in warm water to produce a printing plate. Problems to be Solved by the Invention The present inventors have studied various processing methods for the mono-sheet type DTR type lithographic printing plate using aluminum as a support described in the above patent. I found a problem with this. That is, the lithographic printing plate is used as
It has been found that even if development is carried out using a developer such as that described in the Examples of Specification No. 0491, there is a problem that ink coverage is slow and sufficient printing durability cannot be obtained. An object of the present invention is to solve the above problems and provide a lithographic printing plate with improved ink loading and printing durability. Means for Solving the Problems The above object of the present invention is to provide a lithographic printing method using anodized aluminum as a support and having a physical development nucleus layer and a light-sensitive silver halide photographic emulsion layer thereon. This was achieved by developing the plate with a processing solution in which the content of sodium thiosulfate per liter did not exceed 2 g. [0011] The surface of the aluminum support used in the lithographic printing plate of the present invention may be roughened in order to improve adhesion with the photosensitive layer provided thereon and to improve water retention. be exposed. This surface roughening treatment (so-called graining) is performed by mechanical roughening treatment such as ball graining, wire graining, brush graining, etc., or by chemically dissolving aluminum with chloride, fluoride, etc. There are chemical surface roughening treatments and electrolytic surface roughening treatments performed by electrochemically dissolving aluminum. [0012] After the surface roughening treatment, it is necessary to perform an anodic oxidation treatment. Although conventionally well-known methods can be used for the anodizing treatment, sulfuric acid is used as the most useful electrolyte. Next, phosphoric acid, nitric acid, etc. are also useful electrolytes. Furthermore, JP-A-55-28
Also useful are the sulfuric and phosphoric acid mixtures disclosed in '400. [0013] In the sulfuric acid method, treatment is usually performed using direct current, but alternating current can also be used. The concentration of sulfuric acid is 5~
Used at 30% and 5-25 in the temperature range of 20-60℃
Electrolytic treatment is performed for 0 seconds to provide an oxide film of 1 to 10 g/m2 on the surface. Furthermore, the current density at this time is 1 to 2
0 A/dm2 is preferred. In the case of phosphoric acid method, 5 to 5
It is treated with a current density of 1-15 A/dm2 for 10-300 seconds at a concentration of 0% and a temperature of 30-60°C. [0014] It is preferable to perform a desmut treatment prior to the anodic oxidation treatment. That is, a roughened aluminum substrate was heated with 10-50% hot sulfuric acid (40-60%
℃) or dilute alkali (sodium hydroxide, etc.) to remove the smut attached to the surface. Further, after the anodic oxidation treatment, post-treatment can be performed if necessary. For example, a method of immersion treatment in an aqueous solution of polyvinylphosphonic acid disclosed in British Patent No. 1,230,447 is used. Also,
If necessary, it is possible to provide a hydrophilic polymer undercoat layer, but the choice is made depending on the properties of the photosensitive layer provided thereon. The physical development nuclei of the physical development nucleus layer used in the present invention may be those used in the known silver complex diffusion transfer method, such as colloids such as gold and silver, water-soluble salts such as palladium and zinc, and sulfides. Metal sulfides mixed with can be used. For details and manufacturing methods, see, for example, Focal Press, London and New York (1972), by Andre Lott and Edith Weide.
Photographic Silver Halide Diffusion Processes. Various hydrophilic colloids can be used as protective colloids in the photosensitive silver halide emulsion layer of the printing plate of the present invention. That is, various gelatins such as acid-treated gelatin, alkali-treated gelatin, gelatin derivatives, and grafted gelatin can be used, as well as polyvinylpyrrolidone, various starches, albumin, polyvinyl alcohol,
Hydrophilic polymer compounds such as gum arabic and hydroxyethyl cellulose can be contained. Hydrophilic colloids used include gelatin, gelatin derivatives,
Examples include polyvinyl alcohol, polyvinylpyrrolidone, etc., but it is preferable to use a hydrophilic colloid layer that does not substantially contain a hardening agent in order to facilitate the peelability of the hydrophilic colloid layer after physical development. The types of photosensitive silver halide emulsions used in the present invention include commonly used silver chloride, silver bromide,
It is selected from silver iodide, silver chlorobromide, silver chloroiodobromide, silver iodobromide, and the like. The type of emulsion may be either negative or positive type.
The special type described in No. 4 may also be used. These silver halide emulsions can be chemically or spectrally sensitized as required. As the developing agent used in the present invention, polyhydroxybenzenes and 3-pyrazolidinones are preferred, and these agents may be used in the form of a so-called agent-containing type, which is contained in the constituent layers of the plate material. The developing solution used in the present invention contains alkaline substances such as potassium hydroxide, sodium hydroxide, lithium hydroxide, tertiary sodium phosphate, or amine compounds, preservatives such as sodium sulfite, thickening agents,
For example carboxymethylcessulose, antifoggants such as potassium bromide, toning agents such as 1-phenyl-5-
Additives such as mercaptotetrazole, developer modifying agents, and polyoxyalkylene compounds can be included. The pH of the developer is usually about 10 to 14, preferably about 12 to 14, but the pretreatment (for example, anodization) conditions of the aluminum support of the lithographic printing plate used,
It varies depending on the photographic element, the desired image, the type and amount of various compounds in the developer, development conditions, etc. Wash-off for removing the gelatin layer can be carried out by rinsing with running water at a temperature of about 20 to 30°C. [0023] Example 1 An aluminum plate with a thickness of 0.30 mm was degreased with a 4% aqueous sodium hydroxide solution, and then a 10V alternating current was applied for about 20 minutes in an approximately 1% hydrochloric acid solution. After flowing for a minute, the aluminum plate was immediately anodized with 20% by weight sulfuric acid at a current density of 1 A/dm2 for 5 minutes, and then washed with water and dried to prepare an aluminum plate with an anodized surface. The following physical development nuclear solution was coated onto this support at a coating amount of 10 mg/m2 in terms of silver weight. The physical development nucleus is Carey L.
A gelatin solution was added to the silver sol prepared by method ea) to adjust the weight ratio of silver to gelatin to 1. The coating amount is 50mg/m2. After drying, a photosensitive silver halide emulsion layer having the following composition was coated and dried to prepare a photosensitive lithographic printing plate. Ortho-sensitized silver chloride emulsion (containing 1 mol% silver iodide, average grain size 0.3 μ), silver halide coverage expressed in silver nitrate 2 g/m2, gelatin coverage 0.4 g/m
2. After imagewise exposing the thus obtained lithographic printing plate from a negative film using a contact exposure meter,
After developing at 20° C. for 10 seconds with a developer substantially free of sodium thiosulfate according to the present invention and a developer containing sodium thiosulfate as a comparative developer as shown in Table 1, immediately rinse with running water for 30 seconds. The gelatin layer was washed off. The density of the image area of the photosensitive printing plate thus obtained was measured using a reflection densitometer. [0027] As can be seen from Table 1, the density of image silver obtained using the developing solution of the present invention in which the content of sodium thiosulfate does not exceed 2 g per liter is as follows: The amount of transferred silver decreased significantly when the content of sodium thiosulfate exceeded 2 g/l, and when the amount of sodium thiosulfate added in the developer was 8 g/l, It can be seen that it is almost impossible to obtain a transferred silver image. Example 2 After the lithographic printing plate of the present invention developed by the method of Example 1 was subjected to wash-off treatment, the following Table 2 was prepared before the plate surface was dry.
Apply the plate surface protection liquid with absorbent cotton, etc. and let it dry. The lithographic printing plates prepared in this way were run on a printing machine A.B. Dick 350CD (trademark of an offset printing machine manufactured by A.B. Dick), and the ink receptivity and printing durability were evaluated using the following methods. are shown in Table 3. [Table 2] [Table 3] [0032] Ink receptivity is evaluated by the number of prints until a print with good image density is obtained by simultaneously starting paper feed while bringing the ink roller into contact with the plate surface. did. The printing durability was evaluated by the number of sheets printed when printing became impossible due to either poor ink coverage in the image area or line skipping. As can be seen from the results in Table 3, 1 of the present invention
Lithographic printing plates treated with a developer containing no more than 2 g of sodium thiosulfate per liter have good ink transfer and extremely high printing durability; It can be seen that the ink coverage of the lithographic printing plates treated with a developer containing no more than 2 g of sodium thiosulfate was significantly reduced, and the printing durability was also significantly reduced as the amount of sodium thiosulfate added increased. [0034] As described above, it is possible to obtain a lithographic printing plate having good ink coverage and extremely high printing durability.
Claims (1)
ウムを用い、その上に物理現像核層及び感光性ハロゲン
化銀写真乳剤層を有する平版印刷版において、1l当た
りのチオ硫酸ナトリウムの含有量が2gを越えない処理
液で現像することを特徴とする銀錯塩拡散転写方式を用
いる平版印刷版の処理方法。Claim 1: A lithographic printing plate using anodized aluminum as a support and having a physical development nucleus layer and a light-sensitive silver halide photographic emulsion layer thereon, the content of sodium thiosulfate per liter being 2 g. A method for processing a lithographic printing plate using a silver complex diffusion transfer method, which is characterized by developing with a processing solution that does not exceed .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9957391A JP2960198B2 (en) | 1991-04-03 | 1991-04-03 | Lithographic printing plate processing method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9957391A JP2960198B2 (en) | 1991-04-03 | 1991-04-03 | Lithographic printing plate processing method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04306660A true JPH04306660A (en) | 1992-10-29 |
JP2960198B2 JP2960198B2 (en) | 1999-10-06 |
Family
ID=14250857
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9957391A Expired - Fee Related JP2960198B2 (en) | 1991-04-03 | 1991-04-03 | Lithographic printing plate processing method |
Country Status (1)
Country | Link |
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JP (1) | JP2960198B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0619523A2 (en) * | 1993-04-06 | 1994-10-12 | Fuji Photo Film Co., Ltd. | Method for preparing lithographic printing plate |
EP0772086A1 (en) * | 1995-11-02 | 1997-05-07 | Agfa-Gevaert N.V. | Imaging element for making an improved printing plate according to the silver salt diffusion transfer process |
-
1991
- 1991-04-03 JP JP9957391A patent/JP2960198B2/en not_active Expired - Fee Related
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0619523A2 (en) * | 1993-04-06 | 1994-10-12 | Fuji Photo Film Co., Ltd. | Method for preparing lithographic printing plate |
EP0619523A3 (en) * | 1993-04-06 | 1995-07-19 | Fuji Photo Film Co Ltd | Method for preparing lithographic printing plate. |
EP0772086A1 (en) * | 1995-11-02 | 1997-05-07 | Agfa-Gevaert N.V. | Imaging element for making an improved printing plate according to the silver salt diffusion transfer process |
Also Published As
Publication number | Publication date |
---|---|
JP2960198B2 (en) | 1999-10-06 |
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