JPS63109443A - Developing process method for photosensitive lithographic printing plate improved in stability or the like of developing process - Google Patents
Developing process method for photosensitive lithographic printing plate improved in stability or the like of developing processInfo
- Publication number
- JPS63109443A JPS63109443A JP25628086A JP25628086A JPS63109443A JP S63109443 A JPS63109443 A JP S63109443A JP 25628086 A JP25628086 A JP 25628086A JP 25628086 A JP25628086 A JP 25628086A JP S63109443 A JPS63109443 A JP S63109443A
- Authority
- JP
- Japan
- Prior art keywords
- plate
- developing
- developer
- development
- printing plate
- 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
- 238000000034 method Methods 0.000 title claims abstract description 58
- 238000007639 printing Methods 0.000 title claims abstract description 25
- 238000011161 development Methods 0.000 claims abstract description 42
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 16
- 238000003672 processing method Methods 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 5
- 239000000463 material Substances 0.000 abstract description 5
- 239000004677 Nylon Substances 0.000 abstract description 3
- 229920001778 nylon Polymers 0.000 abstract description 3
- 230000002250 progressing effect Effects 0.000 abstract 1
- 239000008237 rinsing water Substances 0.000 abstract 1
- -1 polyethylene Polymers 0.000 description 26
- 239000004793 Polystyrene Substances 0.000 description 23
- 239000000243 solution Substances 0.000 description 19
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 16
- 238000012545 processing Methods 0.000 description 16
- 239000007788 liquid Substances 0.000 description 14
- 229920005989 resin Polymers 0.000 description 14
- 239000011347 resin Substances 0.000 description 14
- 150000001875 compounds Chemical class 0.000 description 13
- 239000000203 mixture Substances 0.000 description 13
- 238000011282 treatment Methods 0.000 description 11
- 229910052782 aluminium Inorganic materials 0.000 description 10
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 10
- 239000002253 acid Substances 0.000 description 8
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 239000007864 aqueous solution Substances 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- 159000000000 sodium salts Chemical class 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- 150000008049 diazo compounds Chemical class 0.000 description 5
- 239000003960 organic solvent Substances 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
- 239000004115 Sodium Silicate Substances 0.000 description 4
- 239000003513 alkali Substances 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 238000000866 electrolytic etching Methods 0.000 description 4
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 4
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 4
- 229910052911 sodium silicate Inorganic materials 0.000 description 4
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000003945 anionic surfactant Substances 0.000 description 3
- 229930003836 cresol Natural products 0.000 description 3
- 238000000586 desensitisation Methods 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 238000005498 polishing Methods 0.000 description 3
- 238000007788 roughening Methods 0.000 description 3
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 2
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 2
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000004111 Potassium silicate Substances 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- 238000003486 chemical etching Methods 0.000 description 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
- 239000000306 component Substances 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
- 150000002642 lithium compounds Chemical class 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910001507 metal halide Inorganic materials 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 150000002989 phenols Chemical group 0.000 description 2
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 239000002985 plastic film Substances 0.000 description 2
- 229920006255 plastic film Polymers 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 description 2
- 229910052913 potassium silicate Inorganic materials 0.000 description 2
- 235000019353 potassium silicate Nutrition 0.000 description 2
- 229910052814 silicon oxide Inorganic materials 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 150000008054 sulfonate salts Chemical class 0.000 description 2
- ROVRRJSRRSGUOL-UHFFFAOYSA-N victoria blue bo Chemical compound [Cl-].C12=CC=CC=C2C(NCC)=CC=C1C(C=1C=CC(=CC=1)N(CC)CC)=C1C=CC(=[N+](CC)CC)C=C1 ROVRRJSRRSGUOL-UHFFFAOYSA-N 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- JHPBZFOKBAGZBL-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylprop-2-enoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)=C JHPBZFOKBAGZBL-UHFFFAOYSA-N 0.000 description 1
- PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 description 1
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- LMWMTSCFTPQVCJ-UHFFFAOYSA-N 2-methylphenol;phenol Chemical compound OC1=CC=CC=C1.CC1=CC=CC=C1O LMWMTSCFTPQVCJ-UHFFFAOYSA-N 0.000 description 1
- ZRYCRPNCXLQHPN-UHFFFAOYSA-N 3-hydroxy-2-methylbenzaldehyde Chemical compound CC1=C(O)C=CC=C1C=O ZRYCRPNCXLQHPN-UHFFFAOYSA-N 0.000 description 1
- KSOWMDCLEHRQPH-UHFFFAOYSA-N 4-diazocyclohexa-1,5-dien-1-amine Chemical compound NC1=CCC(=[N+]=[N-])C=C1 KSOWMDCLEHRQPH-UHFFFAOYSA-N 0.000 description 1
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 1
- 229920001747 Cellulose diacetate Polymers 0.000 description 1
- DQEFEBPAPFSJLV-UHFFFAOYSA-N Cellulose propionate Chemical compound CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 DQEFEBPAPFSJLV-UHFFFAOYSA-N 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 241001665400 Coracias abyssinicus Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 241000519995 Stachys sylvatica Species 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 235000012501 ammonium carbonate Nutrition 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- XFOZBWSTIQRFQW-UHFFFAOYSA-M benzyl-dimethyl-prop-2-enylazanium;chloride Chemical compound [Cl-].C=CC[N+](C)(C)CC1=CC=CC=C1 XFOZBWSTIQRFQW-UHFFFAOYSA-M 0.000 description 1
- 229960003237 betaine Drugs 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 229920006317 cationic polymer Polymers 0.000 description 1
- 229920006218 cellulose propionate Polymers 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 239000012954 diazonium Substances 0.000 description 1
- BJZIJOLEWHWTJO-UHFFFAOYSA-H dipotassium;hexafluorozirconium(2-) Chemical compound [F-].[F-].[F-].[F-].[F-].[F-].[K+].[K+].[Zr+4] BJZIJOLEWHWTJO-UHFFFAOYSA-H 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical compound [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- JMGZBMRVDHKMKB-UHFFFAOYSA-L disodium;2-sulfobutanedioate Chemical compound [Na+].[Na+].OS(=O)(=O)C(C([O-])=O)CC([O-])=O JMGZBMRVDHKMKB-UHFFFAOYSA-L 0.000 description 1
- 229960000878 docusate sodium Drugs 0.000 description 1
- KWKXNDCHNDYVRT-UHFFFAOYSA-N dodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1 KWKXNDCHNDYVRT-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229940031993 lithium benzoate Drugs 0.000 description 1
- LDJNSLOKTFFLSL-UHFFFAOYSA-M lithium;benzoate Chemical compound [Li+].[O-]C(=O)C1=CC=CC=C1 LDJNSLOKTFFLSL-UHFFFAOYSA-M 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229940050176 methyl chloride Drugs 0.000 description 1
- BXWNKGSJHAJOGX-UHFFFAOYSA-N n-hexadecyl alcohol Natural products CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 238000007645 offset printing Methods 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- ATGAWOHQWWULNK-UHFFFAOYSA-I pentapotassium;[oxido(phosphonatooxy)phosphoryl] phosphate Chemical compound [K+].[K+].[K+].[K+].[K+].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O ATGAWOHQWWULNK-UHFFFAOYSA-I 0.000 description 1
- HWGNBUXHKFFFIH-UHFFFAOYSA-I pentasodium;[oxido(phosphonatooxy)phosphoryl] phosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O HWGNBUXHKFFFIH-UHFFFAOYSA-I 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229960005323 phenoxyethanol Drugs 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 239000005518 polymer electrolyte Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 1
- 229960001755 resorcinol Drugs 0.000 description 1
- 238000005488 sandblasting Methods 0.000 description 1
- 238000005201 scrubbing Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229940047670 sodium acrylate Drugs 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 235000019795 sodium metasilicate Nutrition 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- FGDMJJQHQDFUCP-UHFFFAOYSA-M sodium;2-propan-2-ylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=CC2=C(S([O-])(=O)=O)C(C(C)C)=CC=C21 FGDMJJQHQDFUCP-UHFFFAOYSA-M 0.000 description 1
- 230000000392 somatic effect Effects 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- CXVGEDCSTKKODG-UHFFFAOYSA-N sulisobenzone Chemical compound C1=C(S(O)(=O)=O)C(OC)=CC(O)=C1C(=O)C1=CC=CC=C1 CXVGEDCSTKKODG-UHFFFAOYSA-N 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 125000005207 tetraalkylammonium group Chemical group 0.000 description 1
- 150000005622 tetraalkylammonium hydroxides Chemical class 0.000 description 1
- VKFFEYLSKIYTSJ-UHFFFAOYSA-N tetraazanium;phosphonato phosphate Chemical compound [NH4+].[NH4+].[NH4+].[NH4+].[O-]P([O-])(=O)OP([O-])([O-])=O VKFFEYLSKIYTSJ-UHFFFAOYSA-N 0.000 description 1
- RYCLIXPGLDDLTM-UHFFFAOYSA-J tetrapotassium;phosphonato phosphate Chemical compound [K+].[K+].[K+].[K+].[O-]P([O-])(=O)OP([O-])([O-])=O RYCLIXPGLDDLTM-UHFFFAOYSA-J 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 239000001226 triphosphate Substances 0.000 description 1
- 235000011178 triphosphate Nutrition 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000012224 working solution Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/26—Processing photosensitive materials; Apparatus therefor
- G03F7/30—Imagewise removal using liquid means
- G03F7/3042—Imagewise removal using liquid means from printing plates transported horizontally through the processing stations
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は感光性平版印刷版の現像処理方法に関し、より
詳しくは常に安定した現像処理を行い得るよう改良され
た感光性平版印刷版の現像処理方法に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a method for developing a photosensitive lithographic printing plate, and more specifically to a method for developing a photosensitive lithographic printing plate that has been improved so that stable development can be carried out at all times. Regarding processing method.
露光済みの感光性平版印刷版(以下、25版と称す)を
多数枚処理する場合には、自動現像機を用いることが一
般的であり、同時に用いられる現像処理液は臭いや環境
保全の問題等から水を主たる溶媒とする現像液が主流と
なっている。When processing a large number of exposed photosensitive lithographic printing plates (hereinafter referred to as 25th plate), it is common to use an automatic developing machine, and the developing processing solution used at the same time has odor and environmental protection issues. Because of these reasons, developers that use water as the main solvent have become mainstream.
自動現像機において露光済みの25版を処理する場合に
は、25版を水平搬送しながら現像液をスプレー状に吹
付けて現像処理する方法や、多量の現像液を収容した現
像処理槽に25版を湾曲させて搬送しながら浸漬させて
現像処理する方法が行なわれている。こうした処理機に
おいては、いづれも25版を1版処理するのに多量の現
像液を準備する必要があった。また、現像液を経済的に
利用するために循環再利用しており、その開、処理によ
る現像液劣化に加乏て、特に現像液がアルカリ性の場合
には空気中からの炭酸ブスの吸収による現像液劣化が起
こり、しばしば劣化した現像液を交換しなければならず
、現像作業の管理が非常に面倒であった。When processing the exposed 25th plate in an automatic developing machine, there are two methods: developing by spraying a developer while horizontally transporting the 25th plate, or placing the 25th plate in a developing tank containing a large amount of developer. A method is used in which the printing plate is immersed and developed while being conveyed in a curved manner. In all of these processing machines, it is necessary to prepare a large amount of developer to process one plate of 25 plates. In addition, in order to use the developer economically, it is recycled and reused, and in addition to the deterioration of the developer due to opening and processing, especially when the developer is alkaline, it is caused by the absorption of carbon dioxide from the air. Developer solution deterioration occurs, and the deteriorated developer solution often has to be replaced, making the management of the development work extremely troublesome.
また、上記の欠点を改善する目的で、25版を多量の循
環再使用する現像液で処理する場合、補充液を補充して
現像処理を安定に保つ方法が知られており、特開昭50
−144502号、同55−115039号、同58−
95349号等に開示されている。こうした補充方法に
おいても液交換の頻度は減少するものの液交換の必要が
あり、また、補充の精度の問題とPS版間開品種差によ
る補充のふれは解決できなかった。In addition, in order to improve the above-mentioned drawbacks, there is a known method to keep the development process stable by replenishing the replenisher when processing the 25th plate with a large amount of circulating and reusing developer.
-144502, 55-115039, 58-
No. 95349, etc. Even in this replenishment method, although the frequency of liquid exchange is reduced, liquid exchange is still necessary, and problems of replenishment accuracy and replenishment fluctuations due to differences in the types of PS plates developed cannot be solved.
また、その上に補充装置を必要とし、補充装置自体が高
価であるばかりか、補充装置のi$1整、整備等の必要
もあった。In addition, a replenishment device is required, and not only is the replenishment device itself expensive, but the replenishment device also requires $1 maintenance.
また、こうした補充方法の煩わしさを除き、現像液の節
約を目的とした方法が特開昭55−32044号に記載
されている。これは自動現像機内の感光材料移送路に接
近して現像液拡散板を備えた写真現像処理装置に関する
ものであるが、この装置を用いて25版を少量の現像液
で処理する方法には、現像時間の短縮が難かしく迅速処
理ができないという欠点があり、また、搬送する25版
が必ずしも水平とはいかずに多少上下に歪んでいるため
、現像液量が不均一となり易く、現像むらを生じ易く、
処理される25版と現像液拡散板との間隙を調節するの
に手間がかかるという欠点があった。Further, a method for eliminating the troublesome replenishment method and saving developer is described in Japanese Patent Application Laid-open No. 32044/1983. This relates to a photographic processing device that is equipped with a developer diffusion plate close to the photosensitive material transfer path in an automatic processor, but a method for processing plate 25 with a small amount of developer using this device includes: It has the disadvantage that it is difficult to shorten the development time and cannot perform rapid processing.Also, since the 25 plate being conveyed is not necessarily horizontal but is slightly distorted up and down, the amount of developer tends to be uneven, resulting in uneven development. Easy,
There is a drawback that it takes time and effort to adjust the gap between the 25th plate to be processed and the developer diffusion plate.
本発明は前期現像液の補充等に関する種々の問題を解決
し、安定且つ経済的な感光性平版印刷版の現像処理方法
を提供しようとするもので、その第1の目的は、水を主
たる溶媒とする現像液を用いて常に現像処理を安定に保
ち得る25版の現像処理方法を提供することにある。第
2の目的は、現像液管理と液交換の不要な作業性の向上
した感光性平版印刷版の現像処理方法を提供することに
ある。第3の目的は、補充装置および現像補充液の不要
な、安価な25版の現像処理方法を提供することにある
。第4の目的は、少量の現像液を用いても常に均一な仕
上がりを得ることができる25版の現像処理方法を提供
することにある。The present invention aims to solve various problems related to the replenishment of developer solution, etc., and to provide a stable and economical method for developing photosensitive lithographic printing plates. An object of the present invention is to provide a 25-plate development method that can always maintain stable development using a developing solution. A second object is to provide a method for developing a photosensitive lithographic printing plate, which has improved workability and eliminates the need for developer management and solution exchange. A third object is to provide an inexpensive 25-plate development process that does not require a replenisher or developer replenisher. A fourth object is to provide a 25-plate development method that can always produce a uniform finish even when using a small amount of developer.
前記の目的は自動現像機を用いて25版を自動的に搬送
し、実質的に未使用の水を主たる溶媒とする現像液を処
理されるPS版1枚毎にその版面に供給し、現像促進操
作を付加して現像する現像処理方法において、該現像促
進操作が該25版の、搬送方向と直交する方向全面に亘
り擦ることが可能な擦り部材で擦る操作であり、且該実
質的に未使用の現像液を該擦り部材が移動する面内に供
給することを特徴とする25版の現像処理方法によって
達成される。The above purpose is to automatically transport the 25 plates using an automatic developing machine, supply a developer containing substantially unused water as the main solvent to the surface of each PS plate to be processed, and develop the plate. In the development processing method in which development is performed by adding an accelerating operation, the development accelerating operation is an operation of rubbing the 25th plate with a rubbing member capable of rubbing the entire surface in a direction orthogonal to the conveying direction, and the This is achieved by a 25-plate development processing method characterized in that unused developer is supplied within the plane in which the rubbing member moves.
上記実質的に未使用の現像液とは、未使用の現像液と同
等の現像能力を有する現像液を意味し、全く未使用の現
像液の外、未使用現像液にその現像能力を低下させない
範囲内で使用済の現像液を混合して使用することも可能
であり、例えば現像の際未使用液の供給と共に現像液供
給手段の一部から一度使用した現像液を版面に供給して
現像を行う等の“方法をとることもできるが、全量未使
用液を使用することが最も好ましい。The above-mentioned substantially unused developer means a developer that has the same developing ability as an unused developer, and does not reduce the developing ability of an unused developer, in addition to a completely unused developer. It is also possible to use a mixture of used developer solutions within a certain range. For example, during development, a used developer solution can be supplied from a part of the developer supply means to the plate surface along with an unused solution. However, it is most preferable to use the entire amount of unused liquid.
本発明に使用される搬送方向と直交する方向(以下、1
1手方向と略記する)全面に亘り擦ることが可能な擦り
部材で擦ろ操作には、処理される25版の中手力向長さ
より艮いローラ状の擦り部材を用いて回転により擦る方
法、平板状の擦り部材を前後または左右に移動させるこ
とにより、または回転させることにより擦る方法が含ま
れる。この中でも特に擦る操作が一定の1方向のみの往
復又は回転運動による方法が好ましく、例えば前記のロ
ーラ状擦り部材を回転させる方法、処理される13版の
11手方向長さより長い平板状の擦り部材を前後または
左右に移動させる方法が特に好ましい。A direction perpendicular to the conveying direction used in the present invention (hereinafter referred to as 1
For the rubbing operation using a rubbing member that can rub the entire surface (abbreviated as 1-hand direction), a method of rubbing by rotation using a roller-shaped rubbing member whose length in the mid-hand force direction of the 25th plate to be processed is greater than that of the 25th plate being processed. , a method of rubbing by moving a flat rubbing member back and forth or left and right, or by rotating it. Among these, a method in which the rubbing operation is performed by reciprocating or rotating motion in only one direction is particularly preferable, such as a method of rotating the roller-shaped rubbing member described above, or a method of rotating a flat-shaped rubbing member that is longer than the length in the 11-hand direction of the 13th plate to be processed. Particularly preferred is a method in which the object is moved back and forth or left and right.
なお、これらの擦り部材は複数個組み合わせて使用して
もよい。Note that a plurality of these rubbing members may be used in combination.
これらの擦り部材は、例えばブラシ、スボンノ、或いは
布等を用いて作製することができるが、ブラシが特に好
ましく、その材質としてはナイロンが好ましい。These rubbing members can be made using, for example, a brush, a cloth, or a cloth, but a brush is particularly preferable, and the material thereof is preferably nylon.
本発明においては現像液を擦り部材が移動する面内に供
給する必要がある。現像液を供給する方法には複数の細
口を有する管状物からスプレィさせる方法、2枚の板状
体物の間隙から供給する方法、表面を粗面にしたロール
、または板状体部材を介して供給する方法等が含まれ、
これらの方法において、現像液が28版面へ供給される
位置を擦り部材が移動する面上とすればよい、又これら
の゛ 現像液供給系と擦り部材は分離されていても一体
化されていてもよいが、特に本発明においては一体化さ
れでいることが好ましい1例えば平板状のブラシにおい
て、ブラシ間の間隙に現像液供給口があるもの、ローラ
ブラシのブラシ間隙に現像液供給口を有するものが特に
好ましい。In the present invention, it is necessary to supply the developer within the plane in which the rubbing member moves. Methods for supplying the developer include spraying from a tube with multiple narrow openings, supplying from the gap between two plate-like objects, using a roll with a rough surface, or using a plate-like member. It includes the method of supplying, etc.
In these methods, the position where the developer is supplied to the plate surface may be on the surface where the rubbing member moves, and the developer supply system and the rubbing member may be separated or integrated. However, especially in the present invention, it is preferable that the brush be integrated.1 For example, a flat brush having a developer supply port in the gap between the brushes, and a roller brush having a developer supply port in the gap between the brushes. Particularly preferred.
また前記現像液の供給方法は、1つの方法のみを用いて
もよいし、2つ以上の方法を組み合わせて用いてもよい
。Further, as the developer supply method, only one method may be used, or two or more methods may be used in combination.
これらの方法によって供給される現像液の量は18版1
枚当り一定量、PS版の面積に比例した量、あるいは処
理するPS版の長さ又は幅に比例した量とする等種々の
規準によって決めることができ、また処理するPS版の
a順、或いは形成される画像の非画像部面積等に応じて
これを変えることもできる。自動現像機の構造、処理す
るPS版のサイズの種類、PS版や現像液の性質等に応
じて適宜選べばよいが1版当り11以下であることが望
ましい。The amount of developer supplied by these methods is 18 plates 1
It can be determined based on various criteria, such as a fixed amount per sheet, an amount proportional to the area of the PS plate, or an amount proportional to the length or width of the PS plate to be processed. This can also be changed depending on the area of the non-image portion of the image to be formed. The number may be selected as appropriate depending on the structure of the automatic processor, the size of the PS plate to be processed, the properties of the PS plate and developer, etc., but it is preferably 11 or less per plate.
また、現像液供給部はPS版の有無を検出するセンサ等
の検出機構に連動した制御機構を有していて、PS版が
現像部に搬入される前および通過後は停止fi14が働
くようになっていることが望ましい。In addition, the developer supply section has a control mechanism that is linked to a detection mechanism such as a sensor that detects the presence or absence of a PS plate, and a stop fi14 is activated before the PS plate is carried into the development section and after passing through. It is desirable that the
また使用時の現像液の温度は一般的には5℃乃至60℃
、好ましくは10℃乃至45℃、より好ましくは25℃
乃至35℃の範囲である。Also, the temperature of the developer during use is generally 5℃ to 60℃.
, preferably 10°C to 45°C, more preferably 25°C
The temperature ranges from 35°C to 35°C.
現像液は使用液に仕上げられたものを貯蔵槽に貯えてお
き、処理時に25版上に供給してもよく、また原液と稀
釈液、又は連成を異にする複数の液に分けて貯蔵槽に貯
え各液を版面上に供給し、或いは供給時自動的に混合し
て使用液に仕上げて供給してもよく、自動的に混合し均
一状態として版面に供給してもよい。The developing solution can be stored in a storage tank after it has been finished as a working solution and supplied onto the 25th plate during processing, or it can be stored separately as a stock solution, a diluted solution, or multiple solutions with different combinations. The liquids may be stored in a tank and supplied onto the printing plate, or may be automatically mixed at the time of supply to finish the liquid as a working liquid, or may be automatically mixed and supplied to the printing plate in a uniform state.
又、本発明の方法の実施に用いられる自動現像機は前記
現像処理工程の他に必要ならば現像処理工程後、現像停
止処理工程(停止処理液は使い捨て方法や循環使用の方
式を含む)、不感脂化処理工程の各々個々の処理工程、
現像停止処理工程とそれに引続く不感脂化処理工程、或
いは現像停止処理工程と不感脂化処理工程とを同時に行
う例えば特開昭54−8002号記載の処理工程等を含
んでいでもよい。また、現像処理工程および他の工程は
各々複数であってもよく、例えば現像処理工程を第1の
現像処理工程およI/1iS2の現像処理工程に分けて
もよい。また、上述の現像処理工程および現像後の処理
工程において使用済みの不要な液は、廃液として処理さ
れるが、−時的には廃液タンク等を設けることによって
貯薫されることが望まし+11 。In addition to the above-mentioned development process, the automatic developing machine used to carry out the method of the present invention may also carry out, if necessary, a development stop process after the development process (including a method in which the stop process solution is disposable or cyclically used), Each individual treatment step of the desensitization treatment step,
The process may include a development stop treatment step followed by a desensitization treatment step, or a treatment step in which the development stop treatment step and the desensitization treatment step are performed simultaneously, for example, as described in JP-A-54-8002. Further, each of the development processing step and the other steps may be plural. For example, the development processing step may be divided into a first development processing step and an I/1iS2 development processing step. In addition, the unnecessary liquid used in the above-mentioned development process and post-development process is treated as waste liquid, but it is sometimes desirable to store it in a waste liquid tank or the like. .
本発明の方法において用いられるPS版は、水を主たる
fB媒とする現像液で現像処理でさるものであり、光照
射によって溶解性の変化する感光層が支持体上に塗布さ
れているもの、または電子写真方式等によって画像様レ
ジスト層を設は得る溶解性層が支持体上に設けられてい
るものである。The PS plate used in the method of the present invention is one that is developed with a developer containing water as the main fB medium, and has a photosensitive layer whose solubility changes upon light irradiation coated on a support. Alternatively, a soluble layer on which an image-like resist layer can be formed by electrophotography or the like is provided on the support.
前記のPS版に使用される支持体としては、紙、プラス
チック(例えばポリエチレン、ポリプロピレン、ポリス
チレンなど)ラミネート紙、アルミニウム(アルミニウ
ム合金も含む)、亜鉛、鍔などのような金属の板、二酢
酸セルロース、三酢酸セルロース、プロピオン酸セルロ
ース、ポリエチレンテレフタレート、ポリエチレン、ポ
リプロピレン、ポリカーボネート、ポリビニルアセター
ルなどのようなプラスチックのフィルム、上記の如き金
属がラミネートもしくは蒸着された紙もしくはプラスチ
ックフィルム、アルミニウムもしくはクロムメッキが施
された鋼板などが挙げられ、これらのうち特にアルミニ
ウムおよびアルミニウム被覆された複合支持体が好まし
い。Supports used for the PS plate include paper, plastic (e.g. polyethylene, polypropylene, polystyrene, etc.) laminated paper, aluminum (including aluminum alloys), zinc, metal plates such as Tsuba, cellulose diacetate, etc. , plastic films such as cellulose triacetate, cellulose propionate, polyethylene terephthalate, polyethylene, polypropylene, polycarbonate, polyvinyl acetal, etc., paper or plastic films laminated or vapor-deposited with metals such as those mentioned above, aluminum or chrome plated. Among these, aluminum and aluminum-coated composite supports are particularly preferred.
また、アルミニウム材の表面は、保水性を高め感光層と
密着性を向上させる目的で粗面化処理されていることが
望ましい。Further, the surface of the aluminum material is preferably roughened for the purpose of increasing water retention and improving adhesion to the photosensitive layer.
粗面化方法としては、一般に公知のブラシ研摩法、ボー
ル研摩法、電解エツチング、化学的エツチング、液体ホ
ーニング、サンドブラスト等の方法およびこれらの組合
せが挙げられ、好ましくはブラシ研摩法、電解エツチン
グ、化学的エツチングおよび液体ホーニングが挙げられ
、これらのうちで特に電解エツチングの使用を含む粗面
化方法が好ましい。また、電解エツチングの際に用いら
れる電解浴としては、酸、アルカリまたはそれらの塩を
含む水溶液あるいは有機溶剤を含む水性溶液が用いられ
、これらのうちで特に塩酸、wmまたはそれらの塩を含
む電解液が好ましい、さらに粗面化処理の施されたアル
ミニウム板は、必要に応じて酸またはアルカリの水溶液
にてデスマット処理される。こうして得られたアルミニ
ウム板は陽極酸化処理されることが望ましく、特に好ま
しくは、硫酸またはリン酸を含む浴で処理する方法が挙
げられる。また、さらに必要に応じて封孔処理、その他
弗化ジルコニウム酸カリウム水溶液への浸漬などによる
表面処理を行うことができる。Examples of the surface roughening method include generally known methods such as brush polishing, ball polishing, electrolytic etching, chemical etching, liquid honing, and sandblasting, and combinations thereof. Preferably, brush polishing, electrolytic etching, and chemical etching are used. Target etching and liquid honing are mentioned, among which roughening methods involving the use of electrolytic etching are particularly preferred. The electrolytic bath used in electrolytic etching is an aqueous solution containing an acid, an alkali, or a salt thereof, or an aqueous solution containing an organic solvent. A liquid is preferable, and the aluminum plate subjected to the surface roughening treatment is desmutted with an acid or alkali aqueous solution as necessary. It is desirable that the aluminum plate thus obtained be anodized, and particularly preferably, a method of treatment in a bath containing sulfuric acid or phosphoric acid can be mentioned. Furthermore, if necessary, a sealing treatment and other surface treatments such as immersion in a potassium fluorozirconate aqueous solution can be performed.
本発明に使用される28版の感光性組成物は必須成分と
して感光性物質を含んでおり、感光性物質として露光ま
たはその後の現像処理により、その物理的、化学的性質
が変化するもので、例えば露光により現像液に対する溶
解性に差が生じるもの、露光の前後で分子間の接着力に
差が生じるもの、露光またはその後の現像処理により水
および油に対する親和性に差が生じるもの、更に電子写
真方式により画像部を形成できるもの等が使用できる。The 28th edition photosensitive composition used in the present invention contains a photosensitive substance as an essential component, and the physical and chemical properties of the photosensitive substance change upon exposure or subsequent development treatment. For example, there is a difference in solubility in a developer due to exposure, a difference in intermolecular adhesion between before and after exposure, a difference in affinity for water and oil due to exposure or subsequent development, and A device that can form an image area using a photographic method can be used.
感光性物質の代表的なものとしては、例えば感光性ジア
ゾ化合物、感光性アジド化合物、エチレン性不飽和二重
結合を有する化合物、酸触媒で重合を起こすエポキン化
合物、酸で分解するシリルエーテルポリマーやC−0−
C−基を有する化合物と酸発生剤との組合せ等が挙げら
れる。感光性ジアゾ化合物としては、ボッ型のものとし
てO−キノンジアシド化合物、ネガ型のものとして芳香
族ジアゾニウム塩等が挙げられる。0−キノンジアシド
化合物の基体例としては、例えば特開昭47−5303
号、同48−63802号、同48−63803号、同
49−38701号、同56−1044号、同56−1
045号、特公昭41−11222号、同43−284
03号、同45−9610号、同49−17481号、
米国特許第2,797,213号、同第3,048,1
20号、同第3゜188.210号、同第3,454,
400号、同第3,544,323号、同第3,573
,917号、同f53,674,495号、同第3,7
85゜825号、英国特許第1,227,602号、同
第1,251,345号、同第1,267.005号、
同fjS1,329,888号、同第1.330,93
2号、ドイツ特許fjS854 、890号などに記載
されているものを挙げることができ、これらの化合物を
単独あるいは組合せて感光成分として用いた28版に対
して少なくとも本発明を好ましく適用することができる
。これらの感光成分には芳香族ヒドロキシ化合物の0−
キノンジアジドスルホン酸エステルまたは0−キノンノ
アシトカルボン酸エステルおよび芳香族アミ/化合物の
0−キノンジアジドスルホン酸または0−キ/ンノアジ
ドカルポン酸アミドが包含され、また、これら0−キノ
ンジ7ジド化合物を単独で使用したもの、およびアルカ
リ性樹脂と混合し、この混合物を感光層として設けたも
のが包含される。アルカリ可溶性樹脂には、ノボラック
型フェノール樹脂が含まれ、具体的には7エノールホル
ムアルデヒド樹脂、クレゾールホルムアルデヒド樹脂、
フェノールクレゾール混合ホルムアルデヒド樹脂、クレ
ゾールキシレノール混合ホルムアルデヒド84脂などが
含まれる。更に特開昭50−125806号に記されて
いるように、上記のようなフェノール樹脂と共に、t−
ブチル7エ7−ルホルムアルデヒド樹脂のような炭素数
3〜8のアルキル基で置換されたフェノールまたはクレ
ゾールとホルムアルデヒドとの縮合物とを併用したもの
も適用でさる。0−キノンジアジド化合物を感光成分と
する感光層には、必要に応じて更に染料、可塑剤、プリ
ントアウト性能を与える成分などの添加剤を加えること
ができる。Typical photosensitive substances include, for example, photosensitive diazo compounds, photosensitive azide compounds, compounds with ethylenically unsaturated double bonds, Epoquin compounds that polymerize with acid catalysts, silyl ether polymers that decompose with acids, etc. C-0-
Examples include a combination of a compound having a C-group and an acid generator. Examples of the photosensitive diazo compound include an O-quinone diacid compound as a bot-type compound, and an aromatic diazonium salt as a negative-type compound. Examples of substrates for 0-quinonediaside compounds include, for example, Japanese Patent Application Laid-Open No. 47-5303
No. 48-63802, No. 48-63803, No. 49-38701, No. 56-1044, No. 56-1
No. 045, Special Publication No. 41-11222, No. 43-284
No. 03, No. 45-9610, No. 49-17481,
U.S. Patent No. 2,797,213, U.S. Patent No. 3,048,1
No. 20, No. 3 188.210, No. 3,454,
No. 400, No. 3,544,323, No. 3,573
, No. 917, No. f53,674,495, No. 3,7
85°825, British Patent No. 1,227,602, British Patent No. 1,251,345, British Patent No. 1,267.005,
fjS1,329,888, fjS1.330,93
No. 2, German Patent Nos. fjS854 and 890, etc., and the present invention can be preferably applied at least to the 28th plate in which these compounds are used alone or in combination as photosensitive components. . These photosensitive components contain 0-
Included are quinonediazide sulfonic acid esters or 0-quinonenoasidecarboxylic acid esters and aromatic amino/compounds such as 0-quinonediazide sulfonic acid or 0-quinonediazidecarboxylic acid amide; It includes those used alone and those mixed with an alkaline resin and provided with this mixture as a photosensitive layer. Alkali-soluble resins include novolak-type phenolic resins, specifically 7-enol formaldehyde resins, cresol formaldehyde resins,
Includes phenol-cresol mixed formaldehyde resin, cresol xylenol mixed formaldehyde 84 resin, etc. Furthermore, as described in JP-A-50-125806, in addition to the above-mentioned phenolic resin, t-
A combination of a phenol substituted with an alkyl group having 3 to 8 carbon atoms or a condensate of cresol and formaldehyde, such as butyl 7-ethyl formaldehyde resin, is also applicable. If necessary, additives such as dyes, plasticizers, and components imparting printout performance can be added to the photosensitive layer containing the 0-quinonediazide compound as a photosensitive component.
0−キノンノアシト化合物を感光成分とする感光層の単
位面積当りの量は好ましくは約0.5〜7g/I62の
範囲について本発明を適用できる。The present invention can be applied to an amount per unit area of a photosensitive layer containing an 0-quinone noasite compound as a photosensitive component, preferably in the range of about 0.5 to 7 g/I62.
本発明の方法を適用するポジ型28版の画像露光は特に
変える必要はなく常法に従えばよい。There is no particular need to change the image exposure of the positive type 28 plate to which the method of the present invention is applied, and a conventional method may be used.
ネガ型感光層の感光成分の代表的ならのはジアゾ化合物
であり、例えばノアゾニウム塩および/またはp−ジア
ゾフェニルアミンとホルムアルデヒドとの縮合物である
ジアゾ樹脂、特公昭52−7364号に記@されている
p−ノアジノフェニルアミンのフェノール塩またはフル
オロカプリン酸塩等、特公昭49−48001号に記載
されている3−ノトキシノフェニルアミンー4−ノアゾ
ニウムクロライドと4−二トロノブエニルアミンとホル
ムフルrt)’との共重縮合物の有機溶媒可溶性塩から
なるノアゾIf脂、p〜ジアゾノフェニルアミンとホル
ムアルデヒドとの縮合物の2−メトキシ−4−ヒドロキ
シ−5−ベンゾイルベンゼンスルホン酸塩、ρ−ノ7ゾ
ノフェニルアミンとホルムアルデヒドとの縮合物のテト
ラフルオロホウ酸塩、ヘキサフルオロリン酸塩等が挙げ
られる。これらを感光成分とするネガ型PS版に対して
少なくとも本発明を好ましく適用できる。A typical photosensitive component of the negative photosensitive layer is a diazo compound, such as a diazo resin which is a condensate of noazonium salt and/or p-diazophenylamine and formaldehyde, as described in Japanese Patent Publication No. 7364/1983. 3-notoxynophenylamine-4-noazonium chloride and 4-nitronobenylamine described in Japanese Patent Publication No. 49-48001, such as phenol salt or fluorocaprate of p-noazinophenylamine Noazo If fat consisting of an organic solvent soluble salt of a copolycondensate of p~diazonophenylamine and formaldehyde, 2-methoxy-4-hydroxy-5-benzoylbenzene sulfonate of a copolycondensate of p~diazonophenylamine and formaldehyde , tetrafluoroborate, hexafluorophosphate, etc. of a condensate of ρ-7zonophenylamine and formaldehyde. The present invention can be preferably applied at least to negative PS plates containing these as photosensitive components.
これらのジアゾ化合物を単独で使用したもののほかに感
光層の物性を向上させるため、種々の樹脂と混合して用
いたものに対しても本発明を適用できる。かかる樹脂と
しては、シヱラフク、ポリビニルアルコールの誘導体等
のほか特開昭50−118802号中に記載されている
側鎖にアルコール性水酸基を有する共重合体、特開昭5
5−155355号中に記載されているフェノール性水
酸基を側鎖に持つ共重合体が挙げられる。In addition to those in which these diazo compounds are used alone, the present invention can also be applied to those in which they are used in combination with various resins in order to improve the physical properties of the photosensitive layer. Such resins include copolymers having an alcoholic hydroxyl group in the side chain described in JP-A-50-118802, as well as derivatives of polyvinyl alcohol, JP-A-50-118802, etc.
Examples include copolymers having phenolic hydroxyl groups in their side chains, as described in No. 5-155355.
これらの樹脂には下記一般式で示される構造単位を少な
くとも50重量%含む共重合体、一般式
%式%
(式中、R1は水素原子またはメチル基を示し、R2は
水素原子、メチル基、エチル基またはクロロメチル基を
示し、nは1〜10の整数である。)および芳香族性水
酸基を有する単量体単位を1〜80モル%、ならびにア
クリル酸エステルおよび/またはメタクリル酸エステル
単量体単位を5〜90モル%有し、10〜200の酸価
を持つ高分子化合物が包含される。These resins include copolymers containing at least 50% by weight of structural units represented by the following general formula; ethyl group or chloromethyl group, n is an integer of 1 to 10) and 1 to 80 mol% of monomer units having an aromatic hydroxyl group, and acrylic ester and/or methacrylic ester monomer. Included are polymer compounds having 5 to 90 mol% of somatic units and an acid value of 10 to 200.
本発明の現像処理方法が適用されるネガ型PS版の感光
層には、更に染料、可塑剤、プリントアウト性能を4乏
る成分等の添加剤を加えることができる。Additives such as dyes, plasticizers, and components that degrade printout performance can be added to the photosensitive layer of the negative PS plate to which the development method of the present invention is applied.
上記感光層の単位面積当りの量は少なくとも0.1〜7
g/l112の範囲について本発明を適用できる。The amount per unit area of the photosensitive layer is at least 0.1 to 7
The present invention is applicable to the range of 112 g/l.
本発明の現像処理方法で現像するネガ型PS版の画像露
光は特に変える必要はなく常法に従えばよ本発明に用い
られる水を主たる溶媒とする現像液は中性、アルカリ性
、酸性いずれでもよいが、特に現像液がアルカリ性であ
る場合に有用である。There is no particular need to change the image exposure of the negative PS plate to be developed using the development processing method of the present invention, and conventional methods can be followed. However, it is particularly useful when the developer is alkaline.
アルカリ性現像液のうち、ジアゾ化合物等を感光性物質
としたネガ型PS版に対しては、アルカリ剤、有機溶剤
、アニオン型界面活性剤、亜硫酸塩等を水を溶媒として
含ませたものが好ましく用いられる6 アルカリ剤と
しては、ケイ酸ナトリウム、ケイ酸カリウム、水酸化ナ
トリウム、水酸化リチウム、第三リン酸ナトリウム、第
ニリン酸ナトリウム、第三リン酸カリウム、第ニリン酸
カリウム、第三リン酸アンモニウム、第ニリン酸アンモ
ニウム、メタケイ酸ナトリウム、重炭酸ナトリウム、炭
酸ナトリウム、炭酸カリウム、炭酸アンモニウムなどの
ような無機アルカリ剤、モノ−、シーまたはトリエタノ
ールアミンおよび水酸化テトラアルキルアンモニアのよ
うな有機アルカリ剤および珪酸アンモニウム等が有用で
ある。アルカリ剤の現像液組成物中における含有量は0
.05〜20重量%の範囲で用いるのが好適であり、よ
り好ましくは0.1〜10重量%である。Among alkaline developers, those containing water as a solvent and an alkali agent, an organic solvent, an anionic surfactant, a sulfite, etc. are preferable for negative-tone PS plates that use a diazo compound or the like as a photosensitive substance. 6 The alkaline agents used include sodium silicate, potassium silicate, sodium hydroxide, lithium hydroxide, sodium triphosphate, sodium diphosphate, potassium triphosphate, potassium diphosphate, and triphosphate. Inorganic alkaline agents such as ammonium, ammonium diphosphate, sodium metasilicate, sodium bicarbonate, sodium carbonate, potassium carbonate, ammonium carbonate, etc., organic alkalis such as mono-, triethanolamine and tetraalkylammonium hydroxide. and ammonium silicate are useful. The content of alkaline agent in the developer composition is 0.
.. It is suitable to use it in the range of 0.05 to 20% by weight, more preferably 0.1 to 10% by weight.
有WI溶剤としては、エチレングリコールモノフェニル
エーテル、ベンジルアルコール、11−プロピルアルコ
ール等が有用である。有機溶剤の現像液組成物中におけ
る含有量としては、0.5〜15重景%程度に押さえる
のが好適であり、より好ましい範囲としては1〜5重量
%である。As the WI solvent, ethylene glycol monophenyl ether, benzyl alcohol, 11-propyl alcohol, etc. are useful. The content of the organic solvent in the developer composition is preferably kept at about 0.5 to 15% by weight, and more preferably from 1 to 5% by weight.
アニオン型界面活性剤としては、高級アルコール(C,
〜02□)硫酸エステル塩類〔例えば、ラウリルアルコ
ールサルフェートのナトリウム塩、オクチルアルコール
サル7エ一トのナトリウム塩、ラツリルアルコールサル
7エートのアンモニウム塩、[ティーボールB −81
J(商品名、シェル化学製)、第二ナトリウムアルキル
サルフェートなど〕脂肪族アルコールリン酸エステル塩
M(例えば、セチルアルコールリン酸エステルのナトリ
ウム塩など)、アルキルアリールスルホン酸塩′B(例
えばドデシルベンゼンスルホン酸のナトリウム塩、イン
プロピルナフタレンスルホン酸のナトリウム塩、ノナ7
タレンジスルホン酸のナトリウム塩、メタニトロベンゼ
ンスルホン酸のナトリウム塩ナト)、アルキルアミドの
スルホン酸塩類(例えばC,、H3)CONCHzCH
2SO,Naなど)、二基トリウムスルホコハク酸ジオ
クチルエステル、ナトリウムスルホコハク酸ノヘキシル
エステルなど)がある。これらの中で待にスルホン酸塩
類が好適に用いられる。As anionic surfactants, higher alcohols (C,
~02□) Sulfuric acid ester salts [e.g., sodium salt of lauryl alcohol sulfate, sodium salt of octyl alcohol sulfate, ammonium salt of latulyl alcohol sulfate, [T-Ball B-81
J (trade name, manufactured by Shell Chemical Co., Ltd.), secondary sodium alkyl sulfate, etc.] aliphatic alcohol phosphate ester salt M (e.g., sodium salt of cetyl alcohol phosphate ester, etc.), alkylaryl sulfonate 'B (e.g., dodecylbenzene) Sodium salt of sulfonic acid, sodium salt of inpropylnaphthalene sulfonic acid, Nona 7
Sodium salt of taledisulfonic acid, sodium salt of metanitrobenzenesulfonic acid), sulfonate salts of alkylamides (e.g. C, H3) CONCHzCH
2SO, Na, etc.), dioctyl thorium sulfosuccinate, dioctyl sulfosuccinate, nohexyl sodium sulfosuccinate, etc.). Among these, sulfonate salts are most preferably used.
亜硫酸塩は、水溶液で水不溶性ジアゾ樹脂を溶解する働
きを有し、特に疎水性樹脂と組み合わせた感光層から成
るPS版の現像に於いて、91逍後艮期間経時したPS
版でも汚れのない印刷版を作ることができる。亜硫酸塩
としては、ナトリウム、カリウム、リチウムの如きアル
カリ金属およびマグネシウムの如きアルカリ土類金属塩
等が有用である。Sulfite has the function of dissolving water-insoluble diazo resin in an aqueous solution, and is particularly useful in developing PS plates consisting of a photosensitive layer combined with a hydrophobic resin.
Even printing plates can be made without stains. Useful sulfites include alkali metal salts such as sodium, potassium, and lithium, and alkaline earth metal salts such as magnesium.
他方、0−キノンジアシド化合物等を含む感光層を有す
るポジ型感光材料に対しては上記アルカリ剤を通常0.
1〜3011量%、好ましくは0.5〜20重量%含有
した水溶液が用いられ、通常p119〜14の範囲で用
いるのが好ましい。On the other hand, for positive photosensitive materials having a photosensitive layer containing an 0-quinonediaside compound or the like, the alkali agent is usually added at a concentration of 0.
An aqueous solution containing 1 to 3011% by weight, preferably 0.5 to 20% by weight, is used, and it is usually preferable to use it in the range of 119 to 14.
このような現像液には更に現像性能を高めるために以下
のような添加剤を加えることができる。The following additives can be added to such a developer in order to further improve the developing performance.
例えば、特開昭58−75152号記載のNaC4’、
KCl、KBr等の中性塩、特開昭58−19095
2号記載のEDT^、NT^等のキレート剤、特開昭5
9−121336号記載の〔CO(旧1s)s ) C
1s、COCl2・611.0等の錯体、特開昭50−
51324号記載のフルキルナフタレンスルホン酸ナト
リウム、N−テトラデシル−N、N−7ヒドロキシエチ
ルベタイン等のアニオンまたは両性界面活性剤、米国特
許第4,374,920号記載のテトラメチルデシンジ
オール等の非イオン性界面活性剤、特開昭55−959
46号記載のp−ゾメチルアミノメチルボリスチレンの
メチルクロライド4級化物等のカチオニツクボリマー、
特開昭56−142528号記載のビニルベンジルトリ
メチルアンモニウムクロライドとアクリル酸ナトリウム
の共重合体等の両性高号子電解質、特開昭57−192
952号記載の亜硫酸す) +7ウム等の還元性無機塩
、特開昭58−59444号記載の塩化リチウム等の無
機リチウム化合物、特公昭5〇−34442号記載の安
息香酸リチウム等の有機リチウム化合物、特開昭59−
75255号記載の5iSTi等を含む有機金属界面活
性剤、vfrJIY昭59−84241号記載の有機硼
素化合物、ヨーロッパ特許第1oioto号記載のテト
ラアルキルアンモニウムオキサイド等の4a7ンモニウ
ム塩、ベンジルアルコール、エチレングリコールモノフ
ェニルエーテル等の有機溶7’t1等が挙げられる。For example, NaC4' described in JP-A-58-75152,
Neutral salts such as KCl and KBr, JP-A-58-19095
Chelating agents such as EDT^ and NT^ described in No. 2, JP-A No. 5
[CO (formerly 1s)s) C described in No. 9-121336
1s, complexes such as COCl2.611.0, JP-A-1987-
Anionic or amphoteric surfactants such as sodium flukylnaphthalene sulfonate, N-tetradecyl-N, N-7 hydroxyethyl betaine described in US Pat. No. 51324; Ionic surfactant, JP-A-55-959
cationic polymers such as the methyl chloride quaternary product of p-zomethylaminomethylboristyrene described in No. 46;
Ampholytic polymer electrolyte such as a copolymer of vinylbenzyltrimethylammonium chloride and sodium acrylate described in JP-A-56-142528, JP-A-57-192
Reducing inorganic salts such as sulfite described in No. 952) +7um, inorganic lithium compounds such as lithium chloride described in JP-A-58-59444, organic lithium compounds such as lithium benzoate described in JP-A-58-34442 , Japanese Patent Publication No. 1983-
Organometallic surfactants containing 5iSTi etc. described in No. 75255, organoboron compounds described in vfrJIY No. 59-84241, 4a7 ammonium salts such as tetraalkylammonium oxides described in European Patent No. 1 oioto, benzyl alcohol, ethylene glycol monophenyl Examples include organic solvents such as ether 7't1.
以下、実施例によって本発明を具体的に説明する。 Hereinafter, the present invention will be specifically explained with reference to Examples.
実施例1
厚さ0.31IIIlのアルミニウム板を硝酸溶液中で
電気化学的に粗面化し、よく洗浄した後硫酸溶液中で陽
極酸化処理を行って2.5g/n2の酸化皮膜を上記ア
ルミニウム板表面上に形成させた。Example 1 An aluminum plate with a thickness of 0.31III was electrochemically roughened in a nitric acid solution, thoroughly washed, and then anodized in a sulfuric acid solution to form an oxide film of 2.5 g/n2 on the aluminum plate. formed on the surface.
水洗、乾燥後、特開昭56−1044号の実施例に従っ
て合成したレゾルシンベンズアルデヒド樹脂とす7トキ
/ン1,2−ノ7ノ¥−5−スルホニルクロライドとの
エステル化物3重量部、クレゾールホルマリンノボラッ
ク樹脂9重量部およびビクトリア・ピュア・ブルーBO
H(保土谷化学硲♀工業株式会社製)0.12重量部を
2−メトキシエタノール100fifi部に溶解した感
光液を上記支持体上に塗布乾燥し、約2.8g/m2の
感光性層を有するPS版を得た。After washing with water and drying, 3 parts by weight of the esterified product of resorcin benzaldehyde resin synthesized according to the example of JP-A No. 56-1044 and 7-1,2-no-7-5-sulfonyl chloride, and cresol formalin. 9 parts by weight novolac resin and Victoria Pure Blue BO
A photosensitive solution prepared by dissolving 0.12 parts by weight of H (manufactured by Hodogaya Chemical Industry Co., Ltd.) in 100 parts of 2-methoxyethanol was applied onto the above support and dried to form a photosensitive layer of approximately 2.8 g/m2. A PS version was obtained.
このようにして得られたボッ型28版を800IIII
IIX1003mmの大きさに裁断し多数枚用意した。The Bot type 28 plate obtained in this way is 800III.
A large number of sheets were prepared by cutting them to a size of IIX 1003 mm.
次にこの試料に網点画像面積率が約8096である網点
画像を全面に均一にもつ透明陽画を通じて80c−ノH
離から2KWのメタルハライドランプを用いて60秒間
露光を与えた。露光済試料を第1図に示す自動現像機に
よって現像した。Next, a 80C-NOH was applied to this sample through a transparency having a uniform dot image over the entire surface with a dot image area ratio of about 8096.
Exposure was applied from a distance for 60 seconds using a 2KW metal halide lamp. The exposed sample was developed using an automatic developing machine shown in FIG.
図中Pは露光済のPS版で、PS版は搬送ローラ対1.
2.3によって矢印aの方向に搬送される。ローラ対1
によって現像部に送られたPS版は案内板4上で版面に
現像液パイプ5から現像液を供給され、同時に現像促進
繰作としてナイロンブラシを備えた擦り部材6によって
層面を摩擦して現像される。現像液は現像1ff17に
貯えられでおりポンプ8によって送られる。11!9部
材は図に描かれでいない駆動源によってPS板の進行方
向と直角方向(矢印も方向)に往復運動する。P in the figure is an exposed PS plate, and the PS plate has a transport roller pair 1.
2.3, it is transported in the direction of arrow a. roller vs 1
The PS plate sent to the developing section is placed on a guide plate 4, and a developer is supplied to the plate surface from a developer pipe 5, and at the same time, as a development promotion process, the layer surface is rubbed by a rubbing member 6 equipped with a nylon brush and developed. Ru. The developer is stored in the developer 1ff17 and is sent by the pump 8. The 11!9 member reciprocates in a direction perpendicular to the advancing direction of the PS board (also in the direction of the arrow) by a drive source not shown in the figure.
本機の現像部すなわち擦り部材の実効幅り、は100鎮
−であった。使用済現像液は受け″皿10によって集め
徘棄される。The effective width of the developing section, that is, the rubbing member of this machine was 100 mm. The used developer is collected and disposed of by a receiving tray 10.
現像の終った平版印刷板は搬送ローラ対2によって水洗
部に搬入されてシャワーパイプ11からの水流によって
版面を水洗された後、搬送ローラN3によって機外に排
出される。水洗水は水洗槽12に貯えられポンプ13に
よって循環使用される。After the development has been completed, the lithographic printing plate is transported to a washing section by a pair of transport rollers 2, and the plate surface is washed with water by a stream of water from a shower pipe 11, after which it is discharged out of the machine by a transport roller N3. The washing water is stored in a washing tank 12 and circulated by a pump 13.
現像液槽7に下記組成の現像液を入れ、前記露光済の2
3版試料を搬送方向長さが1003II116となるよ
うに送りで現像を行った。A developer having the following composition is put into the developer tank 7, and the exposed 2
The third plate sample was developed by being fed so that the length in the transport direction was 1003II116.
現像a組成
珪酸ナトリツム水溶’a (SiOz/ Na2Oモル
比1.8、SiO□含有量37.5重量%)
・・・2.9重量部水
・・・17.1重量部得られた版をオフセット印刷機
にかけ印刷したところ良好な印刷物が得られ、特にシャ
ドウ部の細白点のヌケが極めて良く(俗に目の開きが良
いと言う)階調のつ」これのないvt徴が認められた。Development a composition Sodium silicate water soluble 'a (SiOz/Na2O molar ratio 1.8, SiO□ content 37.5% by weight)
...2.9 parts by weight water
...17.1 parts by weight When the obtained plate was printed on an offset printing machine, good prints were obtained, especially the thin white spots in the shadow areas were very well removed (commonly referred to as having a good opening). VT signs with no gradation were observed.
更にPS版試料100枚を連続的に処理し、100枚目
の版について同様の印刷を打った結果も1枚目の版と同
じく良好な印刷物を得ることができた。Further, 100 PS plate samples were continuously processed, and the same printing was performed on the 100th plate, and as a result, a good printed matter was obtained, as was the case with the first plate.
実施例2
厚さ0.241fimの砂目立てしたアルミニウム板を
硫酸中で陽極酸化し、約2g/m2の酸化皮膜をつくり
、よく洗浄した後、珪酸ナトリウム水:PI液に浸漬し
、充分水洗後、乾燥し、下記組成の感光液を塗布した。Example 2 A grained aluminum plate with a thickness of 0.241 fim was anodized in sulfuric acid to form an oxide film of about 2 g/m2, washed thoroughly, then immersed in sodium silicate water: PI solution, and thoroughly washed with water. , dried, and coated with a photosensitive solution having the following composition.
感光液組成
(モル比は上記の順に8,5 : 24 : 60.5
: 7)5.0重f1g
p−ジアゾジフェニルアミンとパラホルムアルデヒドの
縮合物のへキサフルオロリン酸塩0.5重量部
ビクトリアピュアーブルーBOH
(保土ケ谷化学工業(株)!り0.1重量部メチルセロ
ソルブ
100重量部
乾燥後の塗布量は、1.8y/m”であった、このよう
にして得られたネガ型PS版を800mmX 1003
mmの大きさに裁断したものを多数枚用意した。Photosensitive liquid composition (molar ratio is 8.5:24:60.5 in the above order)
: 7) 5.0 parts by weight f1g Hexafluorophosphate of a condensate of p-diazodiphenylamine and paraformaldehyde 0.5 parts by weight Victoria Pure Blue BOH (Hodogaya Chemical Industry Co., Ltd.) 0.1 parts by weight Methyl cellosolve The coating amount after drying 100 parts by weight was 1.8y/m''.The negative PS plate thus obtained was 800mm x 1003
A large number of sheets cut into mm size were prepared.
次いで、この試料に透明陰画を通して50cmの距離か
ら2KWのメタルハライドランプを用いて30秒間露光
した。次に擦り部材が回転ブラシであり、ロール内に現
像液供給口を有するvI造のものを使用した他は同じで
ある第3図に示した自動現像機を用い、現像液槽に下記
組成の現像液を入れ、前記の露光消印刷版を80(hm
/ akin、の速度で搬送し現像した。現像液の供給
量は1販出r) 180x(lに調節した。The sample was then exposed through a transparent negative for 30 seconds from a distance of 50 cm using a 2 KW metal halide lamp. Next, using the same automatic developing machine shown in Figure 3, except that the scrubbing member was a rotating brush and a VI type with a developer supply port inside the roll, the following composition was added to the developer tank. Add a developer and heat the above-mentioned exposed and quenchable printing plate at 80 (hm
It was transported and developed at a speed of /akin. The amount of developer supplied was adjusted to 180x (l).
現像液組成
フェニルセロソルブ 40ffi fl
lノエタ/−ルアミン 10重量部
11−ブチルナフタレンスルホン酸ナトリウム12重量
部
tlY泡削(商品名5N−5512、東しシリコーン(
株)製)0.05重量部
水
937重量部水洗後の版を印刷機にかけ印刷したとこ
ろ良好な印刷物が得られた。Developer composition Phenyl cellosolve 40ffi fl
10 parts by weight of sodium 11-butylnaphthalenesulfonate 12 parts by weight of sodium 11-butylnaphthalene sulfonate
Co., Ltd.) 0.05 parts by weight water
When the plate after washing with 937 parts by weight was printed on a printing machine, good printed matter was obtained.
2枚口以後も同様の現像方法で100枚処理した。After the second sheet, 100 sheets were processed using the same developing method.
100枚目の処理済の版を印刷機にかけ印刷したところ
1枚口と同様の良好な印刷物が得られ、ンヤドウ部の口
の開きも極めて良好であった。When the 100th processed plate was printed on a printing press, a good printed matter similar to that of the first sheet was obtained, and the opening of the edge part was also very good.
実施例3
第5図に示す自動現像機を用い、下記組成の現像液を用
いた他は実施例1と同様の実験を行った結果、実施例1
と同様の良好な印刷物が得られた。Example 3 An experiment similar to Example 1 was conducted using the automatic developing machine shown in Fig. 5 and a developer having the following composition.
Good prints similar to those obtained were obtained.
現像液組成
珪酸カリウム(SiOz/に20モル比1.2.5iO
z含量2重量%)100重量部
イソプロピルナフタレンスルホン酸ナトリウム0.05
重量部
〔発明の効果〕
本発明は処理される感光性平版印刷板上に実質的に未使
mの水系現像液を供給し、特定の現像促進手段と現像液
供給手段により現像処理する方法であるため、従来の現
像液を循環再使用する方法に比べ、常に安定した高品質
の仕上がりを得ることができる。さらに液交換の必要が
なく作業性が者しく向上する。また従来の少量現像液で
処理する方法では成し得なかった均一な仕上がりと迅速
現像を得ることができ、さらに網点品質も高品質なもの
を得ることができる。特にシャドウ部の目の開きが悪か
った従来の少量現像液で処理する方法に比べ、本発明に
おいてはシャドウ部の目の開きが極めて良いという利点
が得られる。さらに本発明においては一つの現像槽で現
像液をとり換えることなく、容易にネガ版およびポジ版
を共通で長期にわたり安定して処理することが可能とな
った。Developer composition Potassium silicate (SiOz/20 molar ratio 1.2.5iO
z content 2% by weight) 100 parts by weight Sodium isopropylnaphthalene sulfonate 0.05
Parts by Weight [Effect of the Invention] The present invention provides a method for supplying substantially unused aqueous developer onto a photosensitive lithographic printing plate to be processed, and carrying out development processing using specific development accelerating means and developer supplying means. Therefore, compared to the conventional method of circulating and reusing the developer, it is possible to always obtain a stable and high-quality finish. Furthermore, there is no need to replace the liquid, and work efficiency is significantly improved. Further, it is possible to obtain a uniform finish and rapid development, which could not be achieved with the conventional processing method using a small amount of developer, and also to obtain high-quality halftone dots. In particular, compared to the conventional method of processing using a small amount of developer, in which the opening of the shadow area was poor, the present invention has the advantage that the opening of the shadow area is extremely good. Furthermore, in the present invention, it has become possible to easily and stably process negative and positive plates in common over a long period of time without replacing the developer in one developer tank.
第1図、第3図、fi5図は本発明の実施例に用いた現
像装置の斜視図、Pt52図は第1図の、第4図はPl
tJ3図の、第6図はfi5図のそれぞれ擦り部材の中
手方向から見た断面図である。
1.2,3・・・搬送ローラ対
5.5゛・・・現像液バイブ
ロ、6・・・擦り部材
7・・・現像a槽Figures 1, 3, and fi5 are perspective views of the developing device used in the embodiment of the present invention, Figure Pt52 is of Figure 1, and Figure 4 is P1.
Fig. tJ3 and Fig. 6 are sectional views of Fig. fi5 as viewed from the middle direction of the rubbing member. 1.2, 3...Transport roller pair 5.5゛...Developer solution vibro, 6...Rubbing member 7...Developer tank a
Claims (2)
搬送し、実質的に未使用の水を主たる溶媒とする現像液
を処理される感光性平版印刷版1枚毎にその版面に供給
し、現像促進操作を付加して現像する現像処理方法にお
いて、該現像促進操作が該感光性平版印刷版の、搬送方
向と直交する方向全面に亘り擦ることが可能な擦り部材
で擦る操作であり、かつ該実質的に未使用の現像液を該
擦り部材が移動する面内に供給することを特徴とする感
光性平版印刷版の現像処理方法。(1) The photosensitive lithographic printing plate is automatically conveyed using an automatic developing machine, and the surface of each photosensitive lithographic printing plate is treated with a developer containing substantially unused water as the main solvent. In the development processing method in which the photosensitive planographic printing plate is supplied to the plate and developed by adding a development accelerating operation, the development accelerating operation is an operation in which the photosensitive planographic printing plate is rubbed with a rubbing member capable of rubbing the entire surface in a direction orthogonal to the conveyance direction. A method for developing a photosensitive lithographic printing plate, characterized in that the substantially unused developer is supplied within the plane in which the rubbing member moves.
面に亘り擦る方法が一定の、1方向のみの往復または回
転運動による方法であることを特徴とする特許請求の範
囲第1項記載の感光性平版印刷版の現像処理方法。(2) Claim 1, characterized in that the method of rubbing the entire surface of the photosensitive lithographic printing plate in a direction orthogonal to the conveyance direction is a method of constant reciprocating or rotational movement in only one direction. A method for developing a photosensitive lithographic printing plate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25628086A JPS63109443A (en) | 1986-10-27 | 1986-10-27 | Developing process method for photosensitive lithographic printing plate improved in stability or the like of developing process |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25628086A JPS63109443A (en) | 1986-10-27 | 1986-10-27 | Developing process method for photosensitive lithographic printing plate improved in stability or the like of developing process |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63109443A true JPS63109443A (en) | 1988-05-14 |
Family
ID=17290451
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP25628086A Pending JPS63109443A (en) | 1986-10-27 | 1986-10-27 | Developing process method for photosensitive lithographic printing plate improved in stability or the like of developing process |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63109443A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5087214A (en) * | 1991-05-21 | 1992-02-11 | United Technologies Automotive, Inc. | Battery terminal connector |
WO1995007498A1 (en) * | 1993-09-04 | 1995-03-16 | Horsell Graphic Industries Limited | Improvements relating to plate rinsing within an image plate processor |
-
1986
- 1986-10-27 JP JP25628086A patent/JPS63109443A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5087214A (en) * | 1991-05-21 | 1992-02-11 | United Technologies Automotive, Inc. | Battery terminal connector |
WO1995007498A1 (en) * | 1993-09-04 | 1995-03-16 | Horsell Graphic Industries Limited | Improvements relating to plate rinsing within an image plate processor |
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