JPS63235938A - Method for processing silver halide photosensitive material - Google Patents
Method for processing silver halide photosensitive materialInfo
- Publication number
- JPS63235938A JPS63235938A JP7096187A JP7096187A JPS63235938A JP S63235938 A JPS63235938 A JP S63235938A JP 7096187 A JP7096187 A JP 7096187A JP 7096187 A JP7096187 A JP 7096187A JP S63235938 A JPS63235938 A JP S63235938A
- Authority
- JP
- Japan
- Prior art keywords
- developer
- silver halide
- silver
- kinds
- compds
- 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
Links
- 229910052709 silver Inorganic materials 0.000 title claims abstract description 39
- 239000004332 silver Substances 0.000 title claims abstract description 39
- 239000000463 material Substances 0.000 title claims abstract description 16
- -1 silver halide Chemical class 0.000 title claims description 28
- 238000000034 method Methods 0.000 title claims description 21
- 238000012545 processing Methods 0.000 title claims description 12
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims abstract description 17
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 5
- 125000003277 amino group Chemical group 0.000 claims abstract 2
- 150000001875 compounds Chemical class 0.000 claims description 10
- 238000011161 development Methods 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 239000007800 oxidant agent Substances 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 238000003672 processing method Methods 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 239000010802 sludge Substances 0.000 abstract description 7
- 230000001603 reducing effect Effects 0.000 abstract description 5
- 230000015572 biosynthetic process Effects 0.000 abstract description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 238000013329 compounding Methods 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 description 10
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000003638 chemical reducing agent Substances 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 239000000523 sample Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 229940090898 Desensitizer Drugs 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 2
- SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 235000010323 ascorbic acid Nutrition 0.000 description 2
- 229960005070 ascorbic acid Drugs 0.000 description 2
- 239000011668 ascorbic acid Substances 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 239000004848 polyfunctional curative Substances 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000011241 protective layer Substances 0.000 description 2
- 238000011946 reduction process Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- GGZHVNZHFYCSEV-UHFFFAOYSA-N 1-Phenyl-5-mercaptotetrazole Chemical compound SC1=NN=NN1C1=CC=CC=C1 GGZHVNZHFYCSEV-UHFFFAOYSA-N 0.000 description 1
- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 102000009027 Albumins Human genes 0.000 description 1
- 108010088751 Albumins Proteins 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 241000283973 Oryctolagus cuniculus Species 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 241000555745 Sciuridae Species 0.000 description 1
- 241000978776 Senegalia senegal Species 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-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
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 239000012496 blank sample Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000011033 desalting Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 210000003743 erythrocyte Anatomy 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 150000002504 iridium compounds Chemical class 0.000 description 1
- FBAFATDZDUQKNH-UHFFFAOYSA-M iron chloride Chemical compound [Cl-].[Fe] FBAFATDZDUQKNH-UHFFFAOYSA-M 0.000 description 1
- WZNJWVWKTVETCG-UHFFFAOYSA-N kojic acid Natural products OC(=O)C(N)CN1C=CC(=O)C(O)=C1 WZNJWVWKTVETCG-UHFFFAOYSA-N 0.000 description 1
- BEJNERDRQOWKJM-UHFFFAOYSA-N kojic acid Chemical compound OCC1=CC(=O)C(O)=CO1 BEJNERDRQOWKJM-UHFFFAOYSA-N 0.000 description 1
- 229960004705 kojic acid Drugs 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 150000004704 methoxides Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002898 organic sulfur compounds Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- CMCWWLVWPDLCRM-UHFFFAOYSA-N phenidone Chemical compound N1C(=O)CCN1C1=CC=CC=C1 CMCWWLVWPDLCRM-UHFFFAOYSA-N 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 229920006267 polyester film 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
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- RWPGFSMJFRPDDP-UHFFFAOYSA-L potassium metabisulfite Chemical compound [K+].[K+].[O-]S(=O)S([O-])(=O)=O RWPGFSMJFRPDDP-UHFFFAOYSA-L 0.000 description 1
- 229940043349 potassium metabisulfite Drugs 0.000 description 1
- 235000010263 potassium metabisulphite Nutrition 0.000 description 1
- BHZRJJOHZFYXTO-UHFFFAOYSA-L potassium sulfite Chemical compound [K+].[K+].[O-]S([O-])=O BHZRJJOHZFYXTO-UHFFFAOYSA-L 0.000 description 1
- 235000019252 potassium sulphite Nutrition 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- NDGRWYRVNANFNB-UHFFFAOYSA-N pyrazolidin-3-one Chemical class O=C1CCNN1 NDGRWYRVNANFNB-UHFFFAOYSA-N 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 150000003567 thiocyanates Chemical class 0.000 description 1
- LTSUHJWLSNQKIP-UHFFFAOYSA-J tin(iv) bromide Chemical compound Br[Sn](Br)(Br)Br LTSUHJWLSNQKIP-UHFFFAOYSA-J 0.000 description 1
- 229940062627 tribasic potassium phosphate Drugs 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229920006186 water-soluble synthetic resin Polymers 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
- G03C5/26—Processes using silver-salt-containing photosensitive materials or agents therefor
- G03C5/29—Development processes or agents therefor
- G03C5/305—Additives other than developers
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Abstract
Description
【発明の詳細な説明】
(N 産業上の利用分野
不発明はハロケン化鈑写真忌元伺科、特に:製版用ハロ
ケン化銀与真感光何S會用いて行う銀画像の現像処理方
法に関するものである。[Detailed Description of the Invention] (N) Industrial application field relates to the field of halocarbon photography, especially: a method for developing silver images using a silver halide photosensitive plate for plate making. It is.
(r+) 従来技術及びその問題点
減力処理とは、ハロゲン化銀写真感光材料を露光、現像
処理した後、画像銀を銀酸化剤で溶解して網点面積率金
工ける方法である。(r+) Prior art and its problems Reduction processing is a method in which a silver halide photographic material is exposed and developed, and then image silver is dissolved with a silver oxidizing agent to improve the dot area ratio.
特に製版用ハロゲン化銀写真感光材料を用いて印刷用の
原版′f:得る際、印刷特性に適した網点階調を得るた
めに、また、より良い色再現を得るために、上記の製版
用写真感光材料に対して減力処理を施し、網点面積を減
少させることによって、画(&に部分的あるいは全面的
に修正することがよく行われる。従って、製版用感光材
料のもつ減力特性能力は銀画像を酸化し、溶解する処理
であり、網点画像を減力処理することによって、網点面
積は減少する。従って、減力処理による網点両像の修正
可能な範囲は網点面積の減少に伴なう網点1個当たりの
黒化濃度の減少の度合いにより制限される。すなわち、
印刷用原版として適当な濃度を保ちつつ、網点面積ヲと
れたけ減少させることか出来るか、ということが減力処
理能力の目安となる。In particular, when obtaining a printing original plate 'f using a silver halide photographic light-sensitive material for plate making, in order to obtain a halftone gradation suitable for the printing characteristics and to obtain better color reproduction, the above plate making method is used. It is often done to partially or completely correct the image (&) by subjecting the photographic light-sensitive material for plate-making to a force-reducing process to reduce the halftone dot area. The characteristic ability is a process that oxidizes and dissolves the silver image, and by applying power reduction processing to the halftone dot image, the halftone dot area is reduced.Therefore, the range in which both halftone images can be corrected by power reduction processing is It is limited by the degree of decrease in blackening density per halftone dot as the dot area decreases.
A measure of the power reduction processing ability is whether the halftone dot area can be reduced as much as possible while maintaining an appropriate density as a printing original plate.
一方、・・ロゲン化銀感光材料の現像処理に用いられる
現像液中には、現像液の保存安定性を高める目的で亜硫
酸塩が使用される事が多い。特に近年広く使用されてい
るラビットアクセス処理では、現像液の保存性を高める
ため、0.1モル/i以上の高濃度の亜硫酸塩を現像液
中に含有させている。On the other hand, sulfites are often used in the developer used for developing silver halide photosensitive materials for the purpose of increasing the storage stability of the developer. Particularly in rabbit access processing, which has been widely used in recent years, a high concentration of sulfite of 0.1 mol/i or more is contained in the developer in order to improve the storage stability of the developer.
このような現像液でハロゲン化銀写真感光材料を処理す
ると、多量の銀錯体が現像液中に溶出し、−溶出された
銀錯体が還元されて銀スラツジとなる。When a silver halide photographic light-sensitive material is processed with such a developer, a large amount of silver complex is eluted into the developer, and the eluted silver complex is reduced to form silver sludge.
特に、自動現像機を用いて、ハロケン化銀写真感光材料
を大量にしかも継続的に処理する場合には、銀スラツジ
が現像ローラーあるいはタンク壁面に付着し、ハロゲン
化銀3真感光材料の表面を汚染し、結果として品質を劣
化させる。In particular, when a large amount of silver halide photographic material is continuously processed using an automatic processor, silver sludge may adhere to the developing roller or the tank wall, and the surface of the silver halide photosensitive material may be coated. contaminate and result in quality deterioration.
このような銀スラツジを防止するために、現1象液中に
メルカフト化合物を添加する方法が知られている。(英
国特許第940,169号、同第1,144.481号
、米国特許3.173.789号、同第3.628,9
55号、特開昭54−13331号、同56−2434
7号、同56−7244.1号、同57−2684−8
号、同57−116340号) しかしながら、このよ
うにメルカスト化合物を現像液中に加えた場合、銀スラ
ツジは防止されるが先に述べた減力特性が、好ましいレ
ベルに達しないという問題のあることが判った。In order to prevent such silver sludge, a method is known in which a merkaft compound is added to the reaction solution. (British Patent No. 940,169, British Patent No. 1,144.481, U.S. Patent No. 3.173.789, British Patent No. 3.628,9
No. 55, JP-A No. 54-13331, JP-A No. 56-2434
No. 7, No. 56-7244.1, No. 57-2684-8
(No. 57-116340) However, when a Mercast compound is added to the developer in this way, silver sludge is prevented, but there is a problem in that the reduction properties mentioned above do not reach a desirable level. It turns out.
(0) 発明の目的
本発明は、ハロゲン化銀写真感光材料の現像処理方法に
関するものであり、詳しくは製版用ハロゲン化銀写真感
光材料に関して銀スラツジを防止すするとともに印桐特
性に適した好丑しい減力特性を与えるだめの現像処理方
法に関する。(0) Purpose of the Invention The present invention relates to a developing method for a silver halide photographic light-sensitive material, and more specifically, a method for developing a silver halide photographic light-sensitive material for plate making that prevents silver sludge and is suitable for inkling characteristics. This invention relates to a developing method that provides undesirable force reduction characteristics.
(D)発明の構成
本発明省は上記目的を達すべく鋭意研究を重ねた結果、
ハロゲン化銀写真感光材料が画像露光され、アルカリ性
処理液で現塚処理された後、銀酸化剤で減力処理する処
理方法において、現像液中に一般式(■)で表わされる
化合物を二種類以上含む事によって、ハロケン化銀写真
感光材料に関して減力特性に適した好ましい現像処理方
法が得られる事を見出した。(D) Structure of the Invention As a result of intensive research aimed at achieving the above objective, the Ministry of the Invention has found that:
In a processing method in which a silver halide photographic light-sensitive material is imagewise exposed, subjected to a development process with an alkaline processing liquid, and then subjected to a reduction treatment with a silver oxidizing agent, two types of compounds represented by the general formula (■) are added to the developer. It has been found that by including the above-mentioned components, a preferable development process suitable for reducing force characteristics can be obtained for silver halide photographic light-sensitive materials.
(■) x :水素又はO4
−C5の低級Y アルキル基
以下、これらの化合物の具体例を示すか、本発明にこれ
らに限矩されるものではない。(■) x: Hydrogen or O4
-C5 lower Y alkyl group Specific examples of these compounds will be shown below, but the present invention is not limited to these.
これらの化合物の添加量は二種の化合物の総量が29/
1を越えない範囲で、また、混合比率は1:9〜9:1
(モル比)の範囲で任意に選ぶことが出来る。The amount of these compounds added is such that the total amount of the two types of compounds is 29/
1, and the mixing ratio is 1:9 to 9:1.
It can be arbitrarily selected within the range of (molar ratio).
本発明に用いられるハロゲン化銀乳剤は酸性法、中性法
、又はアンモニア法のどの方法で製造されても良い。多
価金属を含有することも出来る。また、本発明はハロゲ
ン化銀写真乳剤の性質、例えはハロゲン化銀の組成(例
えば、臭化錫、塩化銀、塩臭化銀、沃臭化銀、塩沃臭化
銀)や、ハロゲン化銀の結晶形、晶癖、大きさに関係な
〈実施出来る。The silver halide emulsion used in the present invention may be produced by any of the acid method, neutral method, and ammonia method. It can also contain polyvalent metals. The present invention also relates to the properties of silver halide photographic emulsions, such as the composition of silver halide (for example, tin bromide, silver chloride, silver chlorobromide, silver iodobromide, silver chloroiodobromide), and It can be carried out regardless of silver crystal shape, crystal habit, and size.
本発明で用いられる乳剤中には各種の添加剤を含有する
ことができる。たとえは、化学増感剤(たとえは、チオ
尿素、ハイポなどの買増感剤、金、白金、イリジウム化
合物などの貴金属増感沖]、還元増感剤)、有機減感剤
等も併用して用いることができる。又、分光増感MIJ
、強色増感剤、安定所り、カブリ防止片]、界面活性片
J、現像沖」、現像促進潮、硬膜剤、硬膜促進剤、色素
液改良剤、増白剤、増粘剤及びこれらのプレカーサー等
を含有することができる。The emulsion used in the present invention can contain various additives. For example, chemical sensitizers (for example, sensitizers such as thiourea and hypo, noble metal sensitizers such as gold, platinum, and iridium compounds), reduction sensitizers, and organic desensitizers are also used. It can be used as In addition, spectral sensitization MIJ
, super sensitizer, stable area, anti-fogging piece], surfactant piece J, developer oki', development accelerator, hardener, hardening accelerator, dye solution improver, whitening agent, thickener and their precursors.
本発明に用いられるハロゲン化銀乳剤の保護コロイドと
してはゼラチン、変性セラチン、アルブミン、寒天、ア
ラビアゴム、アルギン酸等の天然物、ポリビニルアルコ
ール、ポリビニルピロリドン、アクリルアマイドとアク
リル酸とビニルイミダゾールの共重合物等の水溶性合成
樹脂があけられる。Protective colloids for the silver halide emulsion used in the present invention include gelatin, modified seratin, albumin, agar, gum arabic, natural products such as alginic acid, polyvinyl alcohol, polyvinylpyrrolidone, and copolymers of acrylamide, acrylic acid, and vinylimidazole. Water-soluble synthetic resins such as
本発明に用いられるハロゲン化銀写真乳剤は、適当な支
持体、例えはカラス、酢酸セルロースフィルム、ホリエ
チレンテレフタレートフイルム、紙、バライク塗慎紙、
ポリオレフィン(例えは、ポリエチレン、ポリピロピレ
ン等)被覆紙の如きものの土に塗布される。これらの支
持体は、公知の方法でコロナ処理されてもよく、又、必
要に応じて公知の方法で下引加工されても良い。The silver halide photographic emulsion used in the present invention can be prepared on a suitable support, such as glass, cellulose acetate film, polyethylene terephthalate film, paper, barique coated paper,
A polyolefin (eg, polyethylene, polypropylene, etc.) coated soil is applied to the soil, such as paper. These supports may be corona treated by a known method, and may also be undercoated by a known method if necessary.
本発明に用いられるハロゲン化銀写真乳剤は必要に応じ
て保護層、中間層、紫外線吸収層、下塗層あるいは他の
ハロゲン化銀乳剤とともに塗設される。The silver halide photographic emulsion used in the present invention is coated with a protective layer, an intermediate layer, an ultraviolet absorbing layer, an undercoat layer or other silver halide emulsions, if necessary.
本発明に用いられる水性アルカリ現像液としては、一般
に知られている組成のものを用いることができる。現像
主薬としてはジヒドロキシペンセン類(例えはハイドロ
キノン)、3−ピラゾリドン類(例えは1−フェニル−
3−ピラゾリドン)、アミンフェノール類、アスコルビ
ン酸等が単独にあるいは組合わせて用いられる。As the aqueous alkaline developer used in the present invention, those having generally known compositions can be used. As developing agents, dihydroxypencenes (e.g. hydroquinone), 3-pyrazolidones (e.g. 1-phenyl-
(3-pyrazolidone), amine phenols, ascorbic acid, etc. may be used alone or in combination.
その添加量は005〜0.5モル/1である。The amount added is 0.005 to 0.5 mol/1.
本発明に用いられる水性アルカリ現像液は空気酸化から
現像剤全保護する目的で、亜硫酸塩保恒剤剤を含有して
いる。例えは亜硫酸ナトリウム、亜硫酸カリウム、メタ
重亜硫酸カリウム、重亜硫酸ナトリウム等が添加される
。好ましい添加量は0゜25〜1.00モル/ノである
。The aqueous alkaline developer used in the present invention contains a sulfite preservative for the purpose of completely protecting the developer from air oxidation. For example, sodium sulfite, potassium sulfite, potassium metabisulfite, sodium bisulfite, etc. are added. The preferred amount added is 0.25 to 1.00 mol/no.
本発明に用いられる水性アルカリ現像液は、pHi調整
するための水酸化カリウム、水酸化ナトリウム、炭酸カ
リウム、炭酸ナトリウム、酢酸ナトリウム、第三リン酸
カリウム等を含むことが出来る。The aqueous alkaline developer used in the present invention can contain potassium hydroxide, sodium hydroxide, potassium carbonate, sodium carbonate, sodium acetate, tribasic potassium phosphate, etc. for pH adjustment.
7一
本発明に用いられる水性アルカリ現像液は、カブリの生
成を最小限度に抑えるために、丑た好捷しい写真特性を
得る目的で、必要な有機カブリ防止剤を含むことが出来
る。71 The aqueous alkaline developer used in the present invention can contain the necessary organic antifoggants for the purpose of obtaining favorable photographic properties in order to minimize the formation of fog.
ペンゾトリアゾーノペ 6−ニドロペンズイミダゾール
硝i4.5−メチルベソゾトリアゾーノペ 1−フェニ
ル−2−テトラゾリン−5−チオン、5−フェニルテト
ラソール、1−フェニル−5−メルカブトテトラゾーノ
ペ 5−ニトロインタゾール、6−ニトロインタゾール
等が一般的である。Penzotriazonope 6-nidropenzimidazole 4.5-methylbesozotriazonope 1-phenyl-2-tetrazoline-5-thione, 5-phenyltetrasol, 1-phenyl-5-merkabuto Tetrazonope 5-nitrointasol, 6-nitrointazole, etc. are common.
本発明における水性アルカリ現像液はアスコルビン酸、
ジェタノールアミン、コウジ酸等の酸化防止剤、ニトリ
ロトリ酢酸、エチレンジアミンテトラ酢酸等の硬水軟化
剤、ポリアルキレンメキサイド類、アミン化合物、トリ
エチレングリコール、メタノール等の有機溶剤ヲ含むこ
とが出来る。The aqueous alkaline developer in the present invention includes ascorbic acid,
It can contain antioxidants such as jetanolamine and kojic acid, water softeners such as nitrilotriacetic acid and ethylenediaminetetraacetic acid, polyalkylene methoxides, amine compounds, and organic solvents such as triethylene glycol and methanol.
本発明で用いられる減力液としては多くのものが知られ
ている。例えば、過マンガン酸塩、第2鉄塙、第2セリ
ウム塩、赤血塙、過硫酸塩、重クロム酸塩等の減力剤を
用いた減力液が知られている。Many types of reducing fluids are known for use in the present invention. For example, reducing agents using reducing agents such as permanganates, ferric salts, ceric salts, red blood cells, persulfates, and dichromates are known.
定着液としては、一般によく知られている組成のものを
用いる事が出来る。定着剤としてはチオ研酸塩、チオシ
アン酸塩の他、定着剤として知られている有機イオウ化
合物を使用することが出来る。As the fixer, one having a generally well-known composition can be used. As the fixing agent, in addition to thiodinates and thiocyanates, organic sulfur compounds known as fixing agents can be used.
(E) 実施例
実施例1
塩化鉄95モル%を含む塩臭化銀を通常の方法で混合し
、物理熟成を施して平均粒径0.1μmの粒度分布の狭
い乳剤を得た。この乳剤を脱塩し、再溶解した後に有機
減感剤としてピナクリプ)−ルイエローをハロゲン化銀
1モル当り500η、更に硬膜剤、界面活性剤を加えて
ポリエステルフィルム上に銀として3.5&/m’にな
るように保護層用セラチン液と共に塗布し、乾燥した。(E) Examples Example 1 Silver chlorobromide containing 95 mol % of iron chloride was mixed in a conventional manner and subjected to physical ripening to obtain an emulsion with an average grain size of 0.1 μm and a narrow particle size distribution. After desalting and redissolving this emulsion, Pinacrip Yellow was added as an organic desensitizer at a concentration of 500 η per mole of silver halide, a hardener and a surfactant were added, and the silver was coated on a polyester film at a concentration of 3.5 μm. /m' together with a ceratin solution for a protective layer, and dried.
上記試料に、高圧水銀灯を光源とするプリンターを用い
て150i50%の網点を密着露光した。The sample was subjected to contact exposure with 150i50% halftone dots using a printer using a high-pressure mercury lamp as a light source.
さらに表1に示される5種類の現像液を1/F=成し、
38度20秒の条件で現像処理を行い、定着、乾燥した
。Furthermore, the five types of developing solutions shown in Table 1 are made into 1/F=
Development was performed at 38 degrees for 20 seconds, fixed, and dried.
表−1現像液処方 IIJは同圧7衣わす。Table-1 Developer formulation IIJ has the same pressure of 7.
次に各試料を市販の減力准を用いて減力処理を行った。Next, each sample was subjected to a force reduction process using a commercially available force reducer.
処理条件は20℃で減力時間は10秒から100秒の間
で変化させた。各試料について網点濃度が3.0以上と
いう条件で網点面積率の変化の幅を求めた。これを減力
1陥と呼ぶ。C%)表2に谷拭科(1)〜(5)につい
て測定した減力幅の結果を示す。The treatment conditions were 20° C. and the reduction time was varied between 10 seconds and 100 seconds. For each sample, the range of change in dot area ratio was determined under the condition that the dot density was 3.0 or more. This is called a reduction in force 1. C%) Table 2 shows the results of the force reduction widths measured for Tanifuki (1) to (5).
表−2
衣2の結果かられかる様に、一般式(I)で表わされる
メルカフート化合@を一種類加えた試料((1)〜(4
))は、ブランク試料(5)に比較して若干の減力能力
の同上は見られるものの、作業効率の点から考えると、
さらに巾の広い減力時1午が屋まれる〇仄に、同様のハ
ロケン化嫁感光材料に同様な方法で150勝50%の網
点画像を焼き付けた。Table 2 As can be seen from the results of Cloth 2, samples containing one type of mercahoot compound @ represented by general formula (I) ((1) to (4)
)) shows a slight reduction in force reduction capacity compared to the blank sample (5), but from the point of view of work efficiency,
In addition, when the power was reduced over a wide range, a halftone image of 150% and 50% was printed using the same method on the same halogenated light-sensitive material.
さらVCC84示さnる10種種類処理准を1′F成し
、現像処理(38度20秒)後、定宥、乾燥、減力処理
を行い、同様の方法で減力幅を測定した。Furthermore, 10 types of processing samples indicated by VCC84 were prepared at 1'F, and after development (38 degrees for 20 seconds), constant cooling, drying, and force reduction were performed, and the force reduction width was measured in the same manner.
減力幅の測定結果を表4に示す。Table 4 shows the measurement results of the force reduction width.
P5e−4
@e4かられかるように、一般式(I)の化合物を組み
合わせる事によって、個別に加えた時以上の減力能力(
超加成性)が得られる革がわかる。P5e-4 As seen from @e4, by combining the compounds of general formula (I), the force-reducing ability (
You can find out which leathers can obtain super-additive properties.
(以下余白)
実施例2
実施例1と同様の乳沖」に、同様の方法で150線50
%の網点画保全焼き付けた。さらに表5に示されるよう
な5棹類のリス現像液で処理(20に2分)し、定宥、
乾*抜、減力処理を行い、同様の方法で減力を隅を測足
した。(Left below) Example 2 In the same manner as in Example 1, 150 lines and 50
% halftone image preservation burned. Further, it was treated with 5 kinds of Lith developer as shown in Table 5 (for 2 minutes in 20 minutes), and then fixed.
Dry * removal and force reduction processing were performed, and the force reduction was measured at the corners using the same method.
減力幅の?1I11定結果を表6に示す。What about the reduction width? Table 6 shows the 1I11 results.
次に同様の乳剤に同様の方法で150勝50%の一点画
触を焼き付けた0埒らに表7に示される10ね類の処理
欣で現像処理(20f貌2分)し、定着・乾燥後減力処
理を行い、減力幅を劇ボしたO結果を衣S VC示す。Next, the same emulsion was printed with a 150x50% single-point touch using the same method, and then developed using the 10 types of processing shown in Table 7 (20f x 2 minutes), fixed, and dried. After performing the force reduction process, the result of reducing the force reduction width is shown in SVC.
女−7
表−8
表8から、本発明における化合物の超加成性効果はリス
現恍准においても確められた。Female-7 Table-8 From Table 8, the superadditivity effect of the compound of the present invention was also confirmed in the squirrel present condition.
Claims (1)
液で現像処理された後、銀酸化剤で減力処理する処理方
法において、現像処理液中に一般式〔 I 〕で表わされ
る化合物を二種類以上含む事を特徴とするハロゲン化銀
感光材料の処理方法。 〔 I 〕 ▲数式、化学式、表等があります▼ X:水素又はC_1〜C_5の低級 アルキル基 Y:水素、置換又は無置換の 低級アルキル基、置換又 は無置換のアミノ基。[Scope of Claims] In a processing method in which a silver halide photosensitive material is imagewise exposed, developed with an alkaline processing solution, and then subjected to a reduction treatment with a silver oxidizing agent, a compound represented by the general formula [I] is present in the development solution. A method for processing a silver halide photosensitive material, characterized in that it contains two or more types of compounds. [I] ▲There are mathematical formulas, chemical formulas, tables, etc.▼ X: Hydrogen or lower alkyl group of C_1 to C_5 Y: Hydrogen, substituted or unsubstituted lower alkyl group, substituted or unsubstituted amino group.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7096187A JPS63235938A (en) | 1987-03-24 | 1987-03-24 | Method for processing silver halide photosensitive material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7096187A JPS63235938A (en) | 1987-03-24 | 1987-03-24 | Method for processing silver halide photosensitive material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63235938A true JPS63235938A (en) | 1988-09-30 |
Family
ID=13446620
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP7096187A Pending JPS63235938A (en) | 1987-03-24 | 1987-03-24 | Method for processing silver halide photosensitive material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63235938A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0529526A2 (en) * | 1991-08-22 | 1993-03-03 | Fuji Photo Film Co., Ltd. | Developing solution for silver halide photographic material and method for processing silver halide photographic material by using the same |
-
1987
- 1987-03-24 JP JP7096187A patent/JPS63235938A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0529526A2 (en) * | 1991-08-22 | 1993-03-03 | Fuji Photo Film Co., Ltd. | Developing solution for silver halide photographic material and method for processing silver halide photographic material by using the same |
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