JPH0675192B2 - Photosensitive lithographic printing plate processing method - Google Patents
Photosensitive lithographic printing plate processing methodInfo
- Publication number
- JPH0675192B2 JPH0675192B2 JP59240146A JP24014684A JPH0675192B2 JP H0675192 B2 JPH0675192 B2 JP H0675192B2 JP 59240146 A JP59240146 A JP 59240146A JP 24014684 A JP24014684 A JP 24014684A JP H0675192 B2 JPH0675192 B2 JP H0675192B2
- Authority
- JP
- Japan
- Prior art keywords
- plate
- lithographic printing
- printing plate
- developing
- photosensitive lithographic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000003672 processing method Methods 0.000 title description 6
- 238000000034 method Methods 0.000 claims description 46
- 238000011161 development Methods 0.000 claims description 41
- 238000010828 elution Methods 0.000 claims description 30
- 238000012545 processing Methods 0.000 claims description 19
- 239000000243 solution Substances 0.000 description 32
- 239000000047 product Substances 0.000 description 24
- 229910052782 aluminium Inorganic materials 0.000 description 14
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical group [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 14
- 230000006866 deterioration Effects 0.000 description 13
- 239000000203 mixture Substances 0.000 description 13
- -1 polyethylene terephthalate Polymers 0.000 description 12
- 239000003960 organic solvent Substances 0.000 description 10
- 238000011282 treatment Methods 0.000 description 10
- 230000000694 effects Effects 0.000 description 8
- 229910004298 SiO 2 Inorganic materials 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 230000035945 sensitivity Effects 0.000 description 7
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- 230000007423 decrease Effects 0.000 description 5
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 239000004115 Sodium Silicate Substances 0.000 description 4
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 4
- 239000003513 alkali Substances 0.000 description 4
- 239000003945 anionic surfactant Substances 0.000 description 4
- 150000008049 diazo compounds Chemical class 0.000 description 4
- 230000005660 hydrophilic surface Effects 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 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
- 239000002904 solvent Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- 239000004111 Potassium silicate Substances 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000001569 carbon dioxide Substances 0.000 description 3
- 229910002092 carbon dioxide Inorganic materials 0.000 description 3
- 238000000586 desensitisation Methods 0.000 description 3
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 3
- 238000004090 dissolution Methods 0.000 description 3
- PAZHGORSDKKUPI-UHFFFAOYSA-N lithium metasilicate Chemical compound [Li+].[Li+].[O-][Si]([O-])=O PAZHGORSDKKUPI-UHFFFAOYSA-N 0.000 description 3
- 229910052912 lithium silicate Inorganic materials 0.000 description 3
- 238000007747 plating Methods 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 description 3
- 229910052913 potassium silicate Inorganic materials 0.000 description 3
- 235000019353 potassium silicate Nutrition 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 2
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
- VAJVDSVGBWFCLW-UHFFFAOYSA-N 3-Phenyl-1-propanol Chemical compound OCCCC1=CC=CC=C1 VAJVDSVGBWFCLW-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 description 2
- UDHMTPILEWBIQI-UHFFFAOYSA-N butyl naphthalene-1-sulfonate;sodium Chemical compound [Na].C1=CC=C2C(S(=O)(=O)OCCCC)=CC=CC2=C1 UDHMTPILEWBIQI-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 229940061607 dibasic sodium phosphate Drugs 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- ZPWVASYFFYYZEW-UHFFFAOYSA-L dipotassium hydrogen phosphate Chemical compound [K+].[K+].OP([O-])([O-])=O ZPWVASYFFYYZEW-UHFFFAOYSA-L 0.000 description 2
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- QNVRIHYSUZMSGM-UHFFFAOYSA-N hexan-2-ol Chemical compound CCCCC(C)O QNVRIHYSUZMSGM-UHFFFAOYSA-N 0.000 description 2
- 238000009434 installation Methods 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 229960005323 phenoxyethanol Drugs 0.000 description 2
- 239000002985 plastic film Substances 0.000 description 2
- 229920006255 plastic film Polymers 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- BNHGVULTSGNVIX-UHFFFAOYSA-N 1-(2-ethoxyethoxy)ethanol Chemical compound CCOCCOC(C)O BNHGVULTSGNVIX-UHFFFAOYSA-N 0.000 description 1
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 1
- HMNZROFMBSUMAB-UHFFFAOYSA-N 1-ethoxybutan-1-ol Chemical compound CCCC(O)OCC HMNZROFMBSUMAB-UHFFFAOYSA-N 0.000 description 1
- IBLKWZIFZMJLFL-UHFFFAOYSA-N 1-phenoxypropan-2-ol Chemical compound CC(O)COC1=CC=CC=C1 IBLKWZIFZMJLFL-UHFFFAOYSA-N 0.000 description 1
- HQRWWHIETAKIMO-UHFFFAOYSA-N 1-phenylbutan-1-ol Chemical compound CCCC(O)C1=CC=CC=C1 HQRWWHIETAKIMO-UHFFFAOYSA-N 0.000 description 1
- WAPNOHKVXSQRPX-UHFFFAOYSA-N 1-phenylethanol Chemical compound CC(O)C1=CC=CC=C1 WAPNOHKVXSQRPX-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- WMKLOPKWBZQHHF-UHFFFAOYSA-N 2-butoxyethoxybenzene Chemical compound CCCCOCCOC1=CC=CC=C1 WMKLOPKWBZQHHF-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- UPGSWASWQBLSKZ-UHFFFAOYSA-N 2-hexoxyethanol Chemical compound CCCCCCOCCO UPGSWASWQBLSKZ-UHFFFAOYSA-N 0.000 description 1
- CUZKCNWZBXLAJX-UHFFFAOYSA-N 2-phenylmethoxyethanol Chemical compound OCCOCC1=CC=CC=C1 CUZKCNWZBXLAJX-UHFFFAOYSA-N 0.000 description 1
- JSGVZVOGOQILFM-UHFFFAOYSA-N 3-methoxy-1-butanol Chemical compound COC(C)CCO JSGVZVOGOQILFM-UHFFFAOYSA-N 0.000 description 1
- FSWHSYHYMTVSEL-UHFFFAOYSA-N 4-methoxypentan-1-ol Chemical compound COC(C)CCCO FSWHSYHYMTVSEL-UHFFFAOYSA-N 0.000 description 1
- 101100309761 Aedes aegypti SDR-1 gene Proteins 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
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
- 239000004135 Bone phosphate Substances 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- MRABAEUHTLLEML-UHFFFAOYSA-N Butyl lactate Chemical compound CCCCOC(=O)C(C)O MRABAEUHTLLEML-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- 102100038434 Neuroplastin Human genes 0.000 description 1
- 108700038050 Neuroplastin Proteins 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-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
- 229910000831 Steel Inorganic materials 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- SLINHMUFWFWBMU-UHFFFAOYSA-N Triisopropanolamine Chemical compound CC(O)CN(CC(C)O)CC(C)O SLINHMUFWFWBMU-UHFFFAOYSA-N 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 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
- 239000002253 acid Substances 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- XPNGNIFUDRPBFJ-UHFFFAOYSA-N alpha-methylbenzylalcohol Natural products CC1=CC=CC=C1CO XPNGNIFUDRPBFJ-UHFFFAOYSA-N 0.000 description 1
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 235000012501 ammonium carbonate Nutrition 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 229940010556 ammonium phosphate Drugs 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- 229940072049 amyl acetate Drugs 0.000 description 1
- PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 1
- 238000007743 anodising Methods 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 229940007550 benzyl acetate Drugs 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 230000003139 buffering effect Effects 0.000 description 1
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 1
- 239000001191 butyl (2R)-2-hydroxypropanoate Substances 0.000 description 1
- 229940043232 butyl acetate Drugs 0.000 description 1
- HJZGNWSIJASHMX-UHFFFAOYSA-N butyl acetate;ethane-1,2-diol Chemical compound OCCO.CCCCOC(C)=O HJZGNWSIJASHMX-UHFFFAOYSA-N 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
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000306 component Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 239000012954 diazonium Substances 0.000 description 1
- 229940116349 dibasic ammonium phosphate Drugs 0.000 description 1
- 229940111685 dibasic potassium phosphate Drugs 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 description 1
- 229940043279 diisopropylamine Drugs 0.000 description 1
- BBLSYMNDKUHQAG-UHFFFAOYSA-L dilithium;sulfite Chemical compound [Li+].[Li+].[O-]S([O-])=O BBLSYMNDKUHQAG-UHFFFAOYSA-L 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
- 238000007598 dipping method Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000000866 electrolytic etching Methods 0.000 description 1
- 229940093499 ethyl acetate Drugs 0.000 description 1
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 1
- 229940093858 ethyl acetoacetate Drugs 0.000 description 1
- UKFXDFUAPNAMPJ-UHFFFAOYSA-N ethylmalonic acid Chemical compound CCC(C(O)=O)C(O)=O UKFXDFUAPNAMPJ-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- NGAZZOYFWWSOGK-UHFFFAOYSA-N heptan-3-one Chemical compound CCCCC(=O)CC NGAZZOYFWWSOGK-UHFFFAOYSA-N 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- 150000003951 lactams Chemical class 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- JESHZQPNPCJVNG-UHFFFAOYSA-L magnesium;sulfite Chemical compound [Mg+2].[O-]S([O-])=O JESHZQPNPCJVNG-UHFFFAOYSA-L 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000010297 mechanical methods and process 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
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- YKYONYBAUNKHLG-UHFFFAOYSA-N n-Propyl acetate Natural products CCCOC(C)=O YKYONYBAUNKHLG-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000003287 optical effect Effects 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
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005518 polymer electrolyte Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229940093956 potassium carbonate Drugs 0.000 description 1
- 235000011181 potassium carbonates 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
- 229940090181 propyl acetate Drugs 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229940001593 sodium carbonate Drugs 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 235000019795 sodium metasilicate Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 230000009469 supplementation Effects 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 229940062627 tribasic potassium phosphate Drugs 0.000 description 1
- 229940001496 tribasic sodium phosphate Drugs 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
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene 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
- G03F7/3078—Processing different kinds of plates, e.g. negative and positive plates, in the same machine
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Photosensitive Polymer And Photoresist Processing (AREA)
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処理方法に関し、さらに
詳しくは現像液の液活性を安定に維持し得る感光性平版
印刷版の処理方法に関する。TECHNICAL FIELD The present invention relates to a method for treating a photosensitive lithographic printing plate, and more specifically, a method for treating a photosensitive lithographic printing plate capable of stably maintaining the liquid activity of a developing solution. Regarding
(従来の技術) 一般的に自動現像機により感光性平版印刷版(以下、単
にPS版と呼ぶ)を連続的に処理する場合に、処理の進行
に伴って現像液が消費され、現像活性が低下し、そのた
めにPS版の感度も低下することがある。そしてさらにこ
のままで現像処理を続けると、遂には現像不良を引起す
ことすらある。(Prior Art) Generally, when a photosensitive lithographic printing plate (hereinafter, simply referred to as a PS plate) is continuously processed by an automatic developing machine, the developing solution is consumed as the processing progresses, and the development activity is The sensitivity of the PS plate may also decrease due to the decrease. Further, if the development process is continued as it is, it may even cause defective development.
上記のような現像不良を起す原因としては、感光層の溶
出に伴う現像液の疲労、すなわち処理疲労と、空気中の
炭酸ガスを吸収することによる現像液の疲労、すなわち
経時疲労とを挙げることができる。Examples of the cause of the development failure as described above include fatigue of the developing solution due to elution of the photosensitive layer, that is, processing fatigue, and fatigue of the developing solution by absorbing carbon dioxide in the air, that is, fatigue over time. You can
このような疲労現象を回復させるため現像液の補充方法
としては、例えば特開昭58-95349号公報にも記載されて
いるように、現像ゾーン途中においてセンサーにより現
像液の劣化をPS版の感光層の溶出度合で測定し、この測
定結果に基づいて現像補充液を補充する方法が提案され
ている。As a method of replenishing the developing solution for recovering such a fatigue phenomenon, for example, as described in JP-A-58-95349, deterioration of the developing solution is detected by a sensor in the middle of the developing zone and the PS plate is exposed to light. A method has been proposed in which the layer elution degree is measured, and the development replenisher is replenished based on the measurement result.
具体的にはPS版の現像処理過程において現像液の劣化を
測定し、劣化がある所定のレベル迄低下したときに、一
定量の現像補充液が補充されるような方法である。Specifically, it is a method in which the deterioration of the developing solution is measured in the development process of the PS plate, and a certain amount of the developing replenisher is replenished when the deterioration reaches a predetermined level.
上記の方法における現像液の劣化の測定は、処理に伴な
うPS版の非画像部の感光層の溶出度合を交流インピーダ
ンス計で電気抵抗値として測定したり、あるいは光反射
センサーで支持体表面の反射光として測定することによ
り行われる。The deterioration of the developer in the above method is measured by measuring the elution degree of the photosensitive layer in the non-image area of the PS plate with the AC resistance meter as the electric resistance value, or the surface of the support with a light reflection sensor. It is performed by measuring as reflected light.
しかしながらPS版の支持体あるいは感光層は品種毎に異
なっており、そのために現像液の劣化の程度が同じであ
っても、上述のような方法による測定値はPS版の品種に
より異なってしまう。However, the support or photosensitive layer of the PS plate differs depending on the product type, and therefore, even if the degree of deterioration of the developing solution is the same, the measured value by the method as described above differs depending on the product type of the PS plate.
例えば現像液の劣化の測定をPS版の非画像部の感光層の
溶出度合として電気抵抗値で測定する場合、支持体の種
類により電気抵抗値は明らかに相違する。また支持体の
種類が同じであったとしても、その表面の状態によって
異なる値を示すこともある。For example, when the deterioration of the developing solution is measured by the electric resistance value as the elution degree of the photosensitive layer in the non-image area of the PS plate, the electric resistance value is obviously different depending on the type of the support. Even if the type of the support is the same, it may show different values depending on the surface condition.
例えば支持体がアルミニウムの場合、表面の陽極酸化層
の有無あるいはその厚さによって電気抵抗値は明らかに
相違する。For example, when the support is aluminum, the electric resistance value obviously differs depending on the presence or absence of the anodized layer on the surface or the thickness thereof.
また感光層の種類や膜厚が異なっても、感光層の物性の
相違や溶出度合の差に基因する支持体上に残存する感光
層の量の違いによっても電気抵抗値は明らかに相違す
る。Even if the type and thickness of the photosensitive layer are different, the electric resistance value is obviously different due to the difference in the physical properties of the photosensitive layer and the difference in the amount of the photosensitive layer remaining on the support due to the difference in the elution degree.
さらに現像液の劣化の測定をPS版の非画像部の感光層の
溶出度合として光反射センサーで測定する場合も同様に
PS版の品種の相違による支持体表面の反射率または反射
濃度の違い、あるいは支持体上に残存する感光層の反射
率または反射濃度の違いによって異なる測定値を示す。Furthermore, when measuring the deterioration of the developing solution as the elution degree of the photosensitive layer in the non-image area of the PS plate with a light reflection sensor, the same applies.
The measured values differ depending on the difference in reflectance or reflection density on the surface of the support due to the difference in PS plate type, or the difference in reflectance or reflection density of the photosensitive layer remaining on the support.
従ってこのような現像補充液の補充方法によっては、適
切な補充を行なうことができず、PS版の現像品質は劣化
し、品質のバラツキを生ずることがある。Therefore, depending on the method of replenishing the developing replenisher as described above, appropriate replenishment cannot be performed, and the development quality of the PS plate may deteriorate and the quality may vary.
(発明が解決しようとする問題点) 本発明は、上記の如き欠点を改良し、品種の異なるPS版
を現像処理する場合に、現像液の液活性を常に安定して
維持することができる感光性平版印刷版の処理方法を提
供するものである。(Problems to be Solved by the Invention) The present invention improves the above-mentioned drawbacks, and when developing PS plates of different varieties, it is possible to constantly maintain the liquid activity of the developer stably. A method for processing a lithographic printing plate is provided.
(問題点を解決するための手段) 本発明者等が鋭意研究した結果、上記の問題点は、現像
補充液補充装置を有する自動現像機を用いて露光済み感
光性平版印刷版を自動的に搬送、現像処理し、かつ感光
性平版印刷版の非画像部感光層の少なくとも一部分の溶
出度合を測定し、その測定した溶出度合に応じて現像補
充液を補充する感光性平版印刷版の処理方法において、
上記感光性平版印刷版の品種を検知し、感光性平版印刷
版の品種に応じて予め複数入力しておいた補充条件と対
比せしめ、該補充条件に従って現像補充液を補充する感
光性平版印刷版の処理方法により解決することができ
る。(Means for Solving the Problems) As a result of intensive studies by the present inventors, the above-mentioned problems are caused by automatically exposing an exposed photosensitive lithographic printing plate using an automatic processor having a developing replenisher replenishing device. A method of processing a photosensitive lithographic printing plate, which comprises carrying, developing and measuring the elution degree of at least a part of the non-image area photosensitive layer of the photosensitive lithographic printing plate, and replenishing a developing replenisher according to the measured elution degree At
A photosensitive lithographic printing plate which detects the type of the above-mentioned photosensitive lithographic printing plate and compares it with a replenishment condition that has been input in advance according to the type of the photosensitive lithographic printing plate, and replenishes a developing replenisher according to the replenishing condition. It can be solved by the processing method of.
ただし、本発明と先後願の関係にある先願(特願昭59-5
0343号)との構成の重複を除くため、上記感光性平版印
刷版の品種を検知する手段がインピーダンス値の測定に
よるものである場合を除く。However, the prior application (Japanese Patent Application No. 59-5) having a relationship between the present invention and the prior application
No. 0343), the case where the means for detecting the type of the photosensitive lithographic printing plate is by measuring the impedance value is excluded.
以下、本発明の感光性平版印刷版の処理方法を更に詳し
く説明する。The processing method of the photosensitive lithographic printing plate of the present invention will be described in more detail below.
本発明の処理方法において用いられる感光性平版印刷版
(以下、単にPS版と呼ぶ)は、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であ
る。The photosensitive lithographic printing plate (hereinafter simply referred to as PS plate) used in the processing method of the present invention has a photosensitive layer whose solubility is changed by light irradiation, coated on a support.
上記の支持体としては、紙、プラスチックがラミネート
された紙、アルミニウム、亜鉛、銅等の金属板、ポリエ
チレンテレフタレート、ポリプロピレン、三醋酸セルロ
ースなどのプラスチックフィルム、ならびにクロム、ニ
ッケル等の金属が蒸着もしくはラミネートされた金属
板、紙、プラスチックフィルム等が含まれる。これらの
支持体のうち本発明に係るPS版の支持体としては、アル
ミニウム板が好ましく用いられる。Examples of the support include paper, plastic-laminated paper, metal plates such as aluminum, zinc, and copper, plastic films such as polyethylene terephthalate, polypropylene, and cellulose triacetate, and metals such as chromium and nickel that are vapor-deposited or laminated. Included are metal plates, paper, plastic films and the like. Among these supports, an aluminum plate is preferably used as the support for the PS plate according to the present invention.
アルミニウム材としては、純アルイニウムの他アルミニ
ウムを主成分とする合金、例えばケイ素、マグネシウ
ム、鉄、銅、亜鉛、マンガン、ビスマス、ニッケル等を
含むアルミニウム合金を包含する。Examples of the aluminum material include pure aluminum and alloys containing aluminum as a main component, for example, aluminum alloys containing silicon, magnesium, iron, copper, zinc, manganese, bismuth, nickel and the like.
アルミニウム材としては、圧延法、溶融アルミニウムメ
ッキより製造された板状(箔状のものを含む)のアルミ
ニウム材が使用できる。溶融アルミニウムメッキより製
造されたアルミニウム材は鋼板等の金属板に溶融アルミ
ニウム浴でメッキして、厚さが7μm以上のアルミニウ
ム層を有する板である。As the aluminum material, a plate-shaped (including foil-shaped) aluminum material manufactured by a rolling method or hot dip aluminum plating can be used. An aluminum material manufactured by hot dip aluminum plating is a plate having a thickness of 7 μm or more obtained by plating a metal plate such as a steel plate with a hot aluminum bath.
また、アルミニウム板の表面は砂目形状を形成させるこ
とが望ましい。砂目形状を形成させる方法としては、例
えば機械的方法、電解によりエッチングする方法が挙げ
られる。さらに、砂目形状を形成させたアルミニウム板
は陽極酸化処理を施すことが望ましい。また、さらに封
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望ましい。Further, it is desirable that the surface of the aluminum plate has a grain shape. Examples of the method of forming the grain shape include a mechanical method and an electrolytic etching method. Further, it is desirable that the aluminum plate having the grain shape is subjected to anodizing treatment. Further, it is desirable to further perform a surface treatment such as a sealing treatment and other dipping in an aqueous solution of potassium fluorozirconate.
本発明に使用されるPS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は、露光ま
たはその後の現像処理により、その物質的、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 PS plate photosensitive composition used in the present invention contains a photosensitive substance as an essential component, and the photosensitive substance is one whose physical and chemical properties are changed by exposure or subsequent development treatment. , For example, a difference in solubility in a developing solution due to exposure, a difference in intermolecular adhesion before and after exposure, a difference in affinity for water and oil due to exposure or subsequent development, A material capable of forming an image portion by an electrophotographic method or the like can be used.
そ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、酸触媒で重合を起すエポキシ化合物、酸
で分解するC-O-C-基を有する化合物等が挙げられる。感
光性ジアゾ化合物としては、露光によりアルカリ可溶性
に変化するポジ型のものとしてo−ナフトキノンジアジ
ド化合物、露光により溶解性が減少するネガ型のものと
して芳香族ジアゾニウム塩等が挙げられる。Typical examples thereof include a photosensitive diazo compound, a photosensitive azide compound, a compound having an ethylenically unsaturated double bond, an epoxy compound which undergoes polymerization with an acid catalyst, and a compound having a COC- group which decomposes with an acid. Is mentioned. Examples of the photosensitive diazo compound include an o-naphthoquinonediazide compound as a positive type compound that changes into alkali solubility upon exposure and an aromatic diazonium salt as a negative type compound whose solubility decreases upon exposure.
本発明の方法が適用されるPS版の上記により形成される
感光層には更に染料、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。かかる組
成を有する感光層は適当な溶剤の溶液を使用して支持体
上に塗布される。Additives such as dyes, plasticizers, and components for imparting printout performance can be further added to the photosensitive layer formed as described above of the PS plate to which the method of the present invention is applied. A photosensitive layer having such a composition is coated on a support using a solution of a suitable solvent.
支持体上に設けられる上記感光層の塗布量は0.1〜7g/m2
であり、より好ましくは0.5〜3g/m2である。The coating amount of the photosensitive layer provided on the support is 0.1 to 7 g / m 2
And more preferably 0.5 to 3 g / m 2 .
上記組成になるPS版は透明原図を通してカーボンアーク
灯、水銀灯、メタルハライドランプ、タングステンラン
プ等の活性光線豊富な光源により露光され、次いで湿式
処理による現像処理工程にて現像される。The PS plate having the above composition is exposed through a transparent original image by a light source rich in actinic rays such as a carbon arc lamp, a mercury lamp, a metal halide lamp, and a tungsten lamp, and then developed in a development processing step by wet processing.
本発明において使用される現像液は、PS版に用いる感光
性組成物の種類等により種々変化しうるが、好ましくは
アルカリ剤および有機溶媒の少なくとも一つを含有する
ものである。The developing solution used in the present invention can be variously changed depending on the kind of the photosensitive composition used for the PS plate and the like, but preferably contains at least one of an alkaline agent and an organic solvent.
アルカリ剤としてはケイ酸ナトリウム、ケイ酸カリウ
ム、ケイ酸リチウム、水酸化ナトリウム、水酸化カリウ
ム、水酸化リチウム、水酸化アンモニウム、第三リン酸
ナトリウム、第二リン酸ナトリウム、第三リン酸カリウ
ム、第二リン酸カリウム、第三リン酸アンモニウム、第
二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−、ジ−、
またはトリエタノールアミン、モノ−、ジ−、またはト
リメチルアミン、モノ−、ジ−、またはトリエチルアミ
ン、モノ−、またはジイソプロピルアミン、n−ブチル
アミン、モノ−、ジ−、またはトリイソプロパノールア
ミン、エチレンイミン、エチレンジイミン等の有機アミ
ン化合物等が挙げられる。As the alkaline agent, sodium silicate, potassium silicate, lithium silicate, sodium hydroxide, potassium hydroxide, lithium hydroxide, ammonium hydroxide, sodium triphosphate, dibasic sodium phosphate, potassium triphosphate, Inorganic alkali agents such as potassium dibasic phosphate, tribasic ammonium phosphate, dibasic ammonium phosphate, sodium metasilicate, sodium bicarbonate, sodium carbonate, potassium carbonate, ammonium carbonate, mono-, di-,
Or triethanolamine, mono-, di-, or trimethylamine, mono-, di-, or triethylamine, mono- or diisopropylamine, n-butylamine, mono-, di-, or triisopropanolamine, ethyleneimine, ethylenediyl Examples thereof include organic amine compounds such as min.
特に支持体の親水性表面の上に設けられる感光性組成物
がネガ型のジアゾ化合物を含有する場合(以上ネガ型ジ
アゾPS版と記す。)には、現像液は有機溶媒を含有する
アルカリ性水溶液であることが好ましく、有機溶媒とし
ては20℃における水に対する溶解度が10重量%以下であ
ることがPS版の現像性、インキ着肉性、保水性向上の点
で好ましい。20℃における水に対する溶解度が10重量%
以下の有機溶媒としての一部を例示するならば、例えば
酢酸エチル、酢酸プロピル、酢酸ブチル、酢酸アミル、
酢酸ベンジル、アセト酢酸エチル、エチレングリコール
モノブチルアセテート、マロン酸エチル、乳酸ブチル、
レプリン酸ブチルのようなカルボン酸エステル、エチル
ブチルケトン、メチルイソブチルケトン、シクロヘキサ
ノンのようなケトン類、エチレングリコールモノブチル
エーテル、エチレングリコールモノブチルフェニルエー
テル、エチレングリコールモノベンジルエーテル、エチ
レングリコールモノ−n−ヘキシルエーテル、エチレン
グリコールモノフェニルエーテル、プロピレングリコー
ルモノフエニルエーテル、ベンジルアルコール、エトキ
シエトキシエタノール、メチルフェニルカルビノール、
n−アミルアルコール、メチルアミルアルコール、4−
フェニル−1−ブタノール、β−フェネチルアルコー
ル、3−フェニル−1−プロパノールのようなアルコー
ル類、キシレンのようなアルキル置換芳香族炭化水素、
メチレンジクロライド、エチレンジクロライド、モノク
ロルベンゼンのようなハロゲン化炭化水素などがある。
これらの有機溶媒は一種以上用いてもよい。これら有機
溶媒の中では、エチレングリコールモノフェニルエーテ
ルとベンジルアルコールが特に有効である。また、これ
ら有機溶媒の現像液中における含有量は、好ましくは1
〜20重量%であり、特に2〜10重量%のときに、より好
ましい結果を得る。Especially when the photosensitive composition provided on the hydrophilic surface of the support contains a negative type diazo compound (hereinafter referred to as a negative type diazo PS plate), the developer is an alkaline aqueous solution containing an organic solvent. It is preferable that the organic solvent has a solubility in water at 20 ° C. of not more than 10% by weight from the viewpoint of the developability of the PS plate, the ink receptivity, and the improvement of water retention. Solubility in water at 20 ℃ is 10% by weight
If a part of the following organic solvent is exemplified, for example, ethyl acetate, propyl acetate, butyl acetate, amyl acetate,
Benzyl acetate, ethyl acetoacetate, ethylene glycol monobutyl acetate, ethyl malonate, butyl lactate,
Carboxylic acid esters such as butyl repurinate, ethyl butyl ketone, methyl isobutyl ketone, ketones such as cyclohexanone, ethylene glycol monobutyl ether, ethylene glycol monobutyl phenyl ether, ethylene glycol monobenzyl ether, ethylene glycol mono-n-hexyl Ether, ethylene glycol monophenyl ether, propylene glycol monophenyl ether, benzyl alcohol, ethoxyethoxyethanol, methylphenylcarbinol,
n-amyl alcohol, methyl amyl alcohol, 4-
Alcohols such as phenyl-1-butanol, β-phenethyl alcohol, 3-phenyl-1-propanol, alkyl-substituted aromatic hydrocarbons such as xylene,
There are halogenated hydrocarbons such as methylene dichloride, ethylene dichloride and monochlorobenzene.
One or more of these organic solvents may be used. Among these organic solvents, ethylene glycol monophenyl ether and benzyl alcohol are particularly effective. The content of these organic solvents in the developer is preferably 1
-20% by weight, and particularly 2-10% by weight, more preferable results are obtained.
また、ネガ型ジアゾPS版用の現像液中に含まれるアルカ
リ剤の好ましい含有量は0.005〜4重量%で好ましくは
0.5〜2重量%である。The content of the alkaline agent contained in the developer for negative type diazo PS plate is preferably 0.005 to 4% by weight,
It is 0.5 to 2% by weight.
さらに該ネガ型ジアゾPS版の現像液にはアニオン界面活
性剤、水溶性亜硫酸塩、可溶化剤等を含有させることが
現像性向上の上で好ましい。該アニオン界面活性剤とし
ては、特開昭57-5045号公報に記載されている高級アル
コール硫酸エステル類、脂肪族アルコールリン酸エステ
ル塩類、アルキルアリールスルホン酸塩類、アルキルア
ミドスルホン酸塩類、二塩基脂肪酸エステルのスルホン
酸塩類、アルキルナフタレンスルホン酸塩、アルキルナ
フタレンスルホン酸塩のホルムアルデヒド縮合物などが
挙げられる。これらの中で特にブチルナフタレンスルホ
ン酸ナトリウム、ブチルナフタレンスルホン酸ナトリウ
ムのホルムアルヒデド縮合物は現像時に感光性組成物層
の親水性表面からの分離溶解性が強いため好ましい。こ
れらのアニオン界面活性剤は現像液成分中の含有量とし
て0.5〜10重量%が好ましく、さらに好ましくは1〜5
重量%である。水溶性亜硫酸塩は感光性組成物の副反応
による親水性表面への固着、残留を防ぎ、現像性を向上
させる効果をもつものであり、具体例としては亜硫酸の
アルカリまたはアルカリ土類金属が好ましく、例えば亜
硫酸ナトリウム、亜硫酸カリウム、亜硫酸リチウム、亜
硫酸マグネシウムなどがある。亜硫酸塩の現像液組成物
中における好ましい含有量は0.05〜4重量%でより好ま
しくは0.1〜1重量%である。可溶化剤は前述の20℃の
水に対する溶解度が10%以下の有機溶媒の溶解を補助す
るものであるため、より水易溶性の有機溶媒であるもの
が好ましく、低分子のアルコール類、ケトン類、ラクタ
ム類を用いるのが良い。具体的には、例えばメタノー
ル、エタノール、プルパノール、ブタノール、アセト
ン、メチルエチルケトン、エチレングリコールモノメチ
ルエーテル、エチレングリコールモノエチルエーテル、
メトキシブタノール、エトキシブタノール、4−メトキ
シ−4−メチルブタノール、N−メチルピロリドンなど
が好ましい。可溶化剤の使用量としては、現像液中30重
量%以下とすることが好ましい。Further, in order to improve the developability, it is preferable to add an anionic surfactant, a water-soluble sulfite, a solubilizing agent, etc. to the developer for the negative type diazo PS plate. Examples of the anionic surfactant include higher alcohol sulfates, aliphatic alcohol phosphates, alkylaryl sulfonates, alkylamide sulfonates, and dibasic fatty acids described in JP-A-57-5045. Examples thereof include ester sulfonates, alkylnaphthalenesulfonates, formaldehyde condensates of alkylnaphthalenesulfonates, and the like. Of these, sodium butyl naphthalene sulfonate and formaldehyde condensation product of sodium butyl naphthalene sulfonate are particularly preferable because they have strong separation and solubility from the hydrophilic surface of the photosensitive composition layer during development. The content of these anionic surfactants in the developer component is preferably 0.5 to 10% by weight, more preferably 1 to 5%.
% By weight. The water-soluble sulfite has an effect of preventing sticking to a hydrophilic surface by a side reaction of the photosensitive composition, preventing residue, and improving developability, and specific examples thereof include alkali or alkaline earth metal of sulfite. , For example, sodium sulfite, potassium sulfite, lithium sulfite, magnesium sulfite and the like. The content of sulfite in the developer composition is preferably 0.05 to 4% by weight, more preferably 0.1 to 1% by weight. Since the solubilizer is for assisting the dissolution of the organic solvent having a solubility in water at 20 ° C. of 10% or less, it is preferable that the organic solvent is a water-soluble organic solvent, and low molecular weight alcohols and ketones are preferable. It is better to use lactams. Specifically, for example, methanol, ethanol, purpanol, butanol, acetone, methyl ethyl ketone, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether,
Methoxybutanol, ethoxybutanol, 4-methoxy-4-methylbutanol, N-methylpyrrolidone and the like are preferable. The amount of the solubilizer used is preferably 30% by weight or less in the developer.
また、支持体の親水性表面の上にポジ型のジアゾ化合物
を含む感光性組成物を設ける場合(以下ポジ型ジアゾPS
版と記す。)、現像液はアルカリ性の水性溶液であるこ
とが好ましく、アルカリ剤として好ましくはケイ酸カリ
ウム、ケイ酸リチウム、ケイ酸ナトリウム、水酸化ナト
リウム、水酸化カリウム、水酸化リチウム、第三リン酸
ナトリウム、第二リン酸ナトリウム、第三リン酸カリウ
ム、第二リン酸カリウム、炭酸ナトリウム、炭酸カリウ
ム等が挙げられる。これらの中でもケイ酸カリウム、ケ
イ酸リチウム、ケイ酸ナトリウム等のケイ酸アルカリを
含有する現像液は現像階調性が良好なため最も好まし
く、ケイ酸アルカリの組成がモル比で〔SiO2〕/〔M〕
=0.5〜1.5(ここに〔SiO2〕、〔M〕はそれぞれSiO2の
モル濃度と総アルカリ金属のモル濃度を示す。)であ
り、かつSiO2を0.8〜8重量%含有する現像液が好まし
く用いられる。このケイ酸アルカリ組成のうち、特にモ
ル比で〔SiO2〕/〔M〕=0.5〜0.75であり、かつSiO2
が0.8〜4重量%の現像液は、低濃度のため現像廃液の
中和が容易なことから好ましく用いられ、一方0.75を超
え1.3までのモル比であり、かつSiO2が1〜8重量%の
現像液は緩衝力が高く、処理能力が高いことから好適に
用いられる。When a photosensitive composition containing a positive diazo compound is provided on the hydrophilic surface of the support (hereinafter referred to as positive diazo PS
Write as a version. ), The developer is preferably an alkaline aqueous solution, preferably as an alkali agent, potassium silicate, lithium silicate, sodium silicate, sodium hydroxide, potassium hydroxide, lithium hydroxide, tribasic sodium phosphate, Examples thereof include dibasic sodium phosphate, tribasic potassium phosphate, dibasic potassium phosphate, sodium carbonate, potassium carbonate and the like. Among these, a developer containing an alkali silicate such as potassium silicate, lithium silicate, and sodium silicate is most preferable because of good development gradation, and the composition of the alkali silicate is [SiO 2 ] / [M]
= 0.5-1.5 (where [SiO 2 ] and [M] represent the molar concentration of SiO 2 and the molar concentration of total alkali metal, respectively), and a developer containing 0.8-8 wt% of SiO 2 was used. It is preferably used. Of this alkaline silicate composition, a molar ratio of [SiO 2 ] / [M] = 0.5 to 0.75, and SiO 2
Is preferably used because the developer is easily neutralized due to its low concentration, and the molar ratio is more than 0.75 to 1.3 and SiO 2 is 1 to 8% by weight. The developing solution of (1) has a high buffering power and a high processing capacity, and is therefore preferably used.
また、ポジ型ジアゾPS版の現像液中に、特開昭50-51324
号公報に記されるようにアニオン性界面活性剤および両
面界面活性剤のうち少なくとも一つ含有させることによ
り、または特開昭55-95946号公報、同56-142528号公報
に記されるように高分子電解質を含有させることによ
り、感光性組成物への濡水性を高めたり、階調性をさら
に高めることができ、好ましく用いられる。かかる界面
活性剤の添加量は特に制限はないが、0.003〜3重量%
が好ましく、特に0.006〜1重量%の濃度が好ましい。
さらに該ケイ酸アルカリのアルカリ金属として全アルカ
リ金属中、カリウムを20モル%以上含むことが、現像液
中での不溶物発生が少ないため好ましく、より好ましく
はカリウムを90モル%以上含むことであり、最も好まし
くはカリウムが100モル%の場合である。In addition, in the developer of positive-working diazo PS plate, the method disclosed in JP-A-50-51324
As described in JP-A-55-95946 and JP-A-56-142528, by containing at least one of an anionic surfactant and a double-sided surfactant as described in JP-A-55-95946. By containing the polymer electrolyte, the wettability to the photosensitive composition can be enhanced and the gradation can be further enhanced, and thus it is preferably used. The amount of such a surfactant added is not particularly limited, but 0.003 to 3% by weight
Is preferable, and a concentration of 0.006 to 1% by weight is particularly preferable.
Furthermore, in all alkali metals as the alkali metal of the alkali silicate, it is preferable that the content of potassium is 20 mol% or more, since insoluble matter generation in the developing solution is small, and more preferably 90 mol% or more of potassium is contained. Most preferably, potassium is 100 mol%.
感光性組成物がネガ型であるかポジ型であるかにかかわ
らず、本発明に使用される現像液には消泡剤を含有させ
ることができる。好適な消泡剤には有機シラン化合物が
挙げられる。Whether the photosensitive composition is negative or positive, the developer used in the present invention may contain an antifoaming agent. Suitable defoamers include organosilane compounds.
本発明はおいて上記PS版の処理に用いられる自動現像機
としては、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、不感脂化処理工程のそれぞれ個
々の処理工程、ならびに現像停止処理工程とそれに引続
く不感脂化処理工程、さらには現像停止処理工程と不感
脂化処理工程とを組み合わせた処理工程等を有するもの
を包含するものである。In the present invention, as the automatic developing machine used for processing the PS plate, after the development processing step if necessary in addition to the development processing step, each processing step of the development stop processing step and the desensitization processing step, and It includes those having a development stop treatment step and a subsequent desensitization treatment step, and a treatment step in which the development stop treatment step and the desensitization treatment step are combined.
このような処理工程の例としては、例えば特開昭54-800
2号公報に記載がある。An example of such a processing step is, for example, Japanese Patent Laid-Open No. 54-800.
It is described in Publication No. 2.
本発明の処理方法における現像補充液の補充方法では、
PS版を非画像部感光層の少くとも一部分の溶出度合を測
定するために用いられるセンサーとしては、例えば特開
昭58-95349号公報に記載のあるような光学的あるいは電
気的に測定し得るセンサーを挙げることができる。In the method of replenishing the developing replenisher in the processing method of the present invention,
As a sensor used to measure the elution degree of at least a part of the non-image area photosensitive layer of the PS plate, it can be measured optically or electrically as described in JP-A-58-95349, for example. The sensor can be mentioned.
そしてこれらセンサーの位置については、本発明では現
像ゾーン途中の位置あるいは現像ゾーン通過後の位置の
いずれでもよい。The positions of these sensors may be either in the middle of the developing zone or after passing through the developing zone in the present invention.
上記センサーを現像ゾーン通過後の位置に設けるときの
好ましい実施態様を記載すれば、溶出度合を測定する部
分に対して、その部分の現像を現像ゾーンにおいて一定
時間実質的に進行させない手段を採り、その部分の溶出
度合を現像ゾーン通過後測定する方法、あるいはPS版の
非画像部感光層の一部に突出速度または溶出度合が他の
非画像部感光層と異なる部分を設け、その部分の溶出度
合を現像ゾーン通過後に測定する方法を挙げることがで
きる。If a preferred embodiment when the sensor is provided at a position after passing through the development zone is described, a means for preventing development of that portion from being substantially progressed in the development zone for a certain period is taken with respect to the portion for measuring the elution degree, A method of measuring the elution degree of the part after passing through the development zone, or providing a part of the non-image area photosensitive layer of the PS plate where the protrusion speed or elution degree is different from other non-image area photosensitive layers, and elution of the part A method of measuring the degree after passing through the development zone can be mentioned.
現像ゾーン途中の位置にセンサーを設ける方法は、装置
の簡素化または現像後のPS版の消去の必要性の有無など
の点から現像後にセンサーを設けるよりも好ましい。The method of providing the sensor at a position in the middle of the developing zone is preferable to providing the sensor after the development in view of simplification of the apparatus or the necessity of erasing the PS plate after the development.
本発明によれば現像ゾーン途中の位置にセンサーを設け
る場合のその位置は、現像ゾーンの挿入部から現像の進
む方向に現像ゾーンの1/20程度進行した位置から1/2程
度進行した位置までの範囲内に設けることが好ましい。According to the present invention, when the sensor is provided at a position in the middle of the development zone, the position is from a position advanced about 1/20 of the development zone to a position advanced about 1/2 of the development zone from the insertion portion of the development zone. It is preferable to provide it within the range.
本発明によれば、前記のような方法により測定された溶
出度合に応じて現像補充液を補充する方法において、被
処理PS版の品種を検知することを特徴の1つとするが、
PS版の品種情報を得る方法としては、人為的に品種情報
を得る方法あるいは自動的にセンサーによって品種情報
を得る方法等を挙げることができる。According to the present invention, in the method of replenishing the development replenisher according to the elution degree measured by the above method, one of the features is to detect the type of PS plate to be treated,
Examples of the method for obtaining the PS version type information include a method for artificially obtaining the type information and a method for automatically obtaining the type information by a sensor.
先づ人為的方法について述べれば、例えばPS版の各品種
に対応する選択ボタンを操作する方法もしくは品種が大
きく2つに分けられるときは、1つのグループの品種に
対しては、PS版の端を自動現像機の右端に揃えて処理
し、他のもう1つのグループの品種に対してはPS版の端
を自動現像機の左端に揃えて処理する方法等を挙げるこ
とができる。As for the artificial method, for example, the method of operating the selection buttons corresponding to each PS version product, or when the product types can be roughly divided into two, the PS version ends for one group product type. Can be processed by aligning with the right edge of the automatic processor, and for the other type of product, the edge of the PS plate can be aligned with the left edge of the automatic processor.
またさらに磁気カードなどの中間媒体に品種情報を記憶
させ、PS版の処理時に上記中間媒体をセットし、品種を
検知判別する方法もある。There is also a method of storing product type information in an intermediate medium such as a magnetic card, setting the above-mentioned intermediate medium during processing of a PS plate, and detecting and determining the product type.
これに対して自動的方法では、例えば光学センサーを用
いPS版の反射濃度あるいは反射率を求め、予め記憶させ
ておいた各品種ごとの反射濃度あるいは反射率と比較せ
しめて品種を識別する方法等があげられる。上述の自動
的方法は、手間がかからず、また誤操作がないので人為
的方法に比較して優れており、好ましい。On the other hand, in the automatic method, for example, a method of determining the reflection density or reflectance of the PS plate by using an optical sensor and comparing it with the reflection density or reflectance of each product type stored in advance to identify the product type, etc. Can be given. The above-mentioned automatic method is preferable because it is less troublesome and does not cause an erroneous operation as compared with the artificial method.
以上のほか、例えばPS版の一定の位置あるいは品種別に
異なった位置に小さな切れ込み部などを設けて光学的、
または接触方式でその位置を検出、あるいは形状を確認
して品種を識別する方法もあり、また予めPS版の一部分
に印字されたコードを光学的に読み取る方法とか接触針
方式にてPS版の表面粗さあるいは予め付与された表面凹
凸を検出して品種を識別する方法等もある。In addition to the above, for example, by providing a small notch at a certain position on the PS plate or at a different position for each product type,
There is also a method to detect the position by contact method, or to identify the type by checking the shape, or to optically read the code printed on a part of the PS plate in advance, or the surface of the PS plate by the contact needle method. There is also a method of identifying roughness by detecting roughness or surface irregularities given in advance.
上述の如き品種を識別するためのセンサーを現像液の劣
化度を測定するためのセンサーとそれぞれ別体に設ける
場合には、それぞれのセンサーの種類ならびに位置に特
に限定されるものではなく任意でよい。When the sensor for identifying the product type as described above is provided separately from the sensor for measuring the degree of deterioration of the developer, the type and position of each sensor are not particularly limited and may be arbitrary. .
すなわち、その一例を挙げれば現像液の劣化度をPS版の
非画像部感光層のインピーダンスとして測定するセンサ
ーを現像ゾーン途中の位置に設け、また品種を識別する
ための光反射型のセンさーを現像ゾーン手前の位置に設
ける方法等がある。That is, to give an example, a sensor for measuring the degree of deterioration of the developing solution as the impedance of the non-image area photosensitive layer of the PS plate is provided at a position in the middle of the developing zone, and a light reflection type sensor for identifying the product type. Is provided at a position before the development zone.
本発明によれば、現像ゾーン途中の位置あるいは現像ゾ
ーン通過後の位置に1つのセンサーを設置して非画像部
感光層の溶出度合による現像液の劣化度の測定ならびに
品種の識別を上記の1つのセンサーにより行なうことが
好ましい。According to the present invention, one sensor is installed at a position in the middle of the development zone or a position after passing through the development zone to measure the degree of deterioration of the developing solution due to the elution degree of the non-image area photosensitive layer and to identify the type. It is preferable to use one sensor.
より好ましくは、現像ゾーン途中の位置に1つのセンサ
ーを設け、この1つのセンサーにより現像液の劣化度の
測定ならびに品種の識別を行なうことである。More preferably, one sensor is provided at a position in the middle of the developing zone, and this one sensor measures the degree of deterioration of the developing solution and identifies the product type.
上記のように現像液の劣化度の測定を行なうセンサーと
して電気的に測定するセンサーを用いるときは、センサ
ーの一方の電極ともう一方の電極との距離は0.1mm〜30c
mが好ましく、より好ましくは0.1mm〜15cmである。また
2つの電極の位置関係は、PS版搬送方向に対して平行方
向、垂直方向あるいはPS版をはさんで上下方向いずれの
位置でもよい。また、PS版と電極との距離は10mm以下が
好ましく、より好ましくは5mm以下である。また、PS版
と電極とが平行に並ぶ部分での電極の面積は1cm2〜20cm
2が望ましいが、より好ましくは2cm2〜10cm2である。こ
の時、少なくとも一方の電極はPS版の感光層を有する側
に位置する必要がある。感光層の残存量を交流でのイン
ピーダンスとしてとらえる場合、PS版と電極とが接触す
るか、あるいはPS版電極の間に電解質である液体を介す
るなどして電気が流れ得る状態にしておく必要がある。When using a sensor that electrically measures as the sensor that measures the deterioration degree of the developer as described above, the distance between one electrode of the sensor and the other electrode is 0.1 mm to 30 c.
m is preferable, and more preferably 0.1 mm to 15 cm. Further, the positional relationship between the two electrodes may be parallel to the PS plate transport direction, perpendicular to the PS plate transport direction, or vertically above and below the PS plate. The distance between the PS plate and the electrode is preferably 10 mm or less, more preferably 5 mm or less. The area of the electrode in the part where the PS plate and the electrode are parallel to each other is 1 cm 2 to 20 cm.
2 is preferred, more preferably 2cm 2 ~10cm 2. At this time, at least one of the electrodes needs to be positioned on the side of the PS plate having the photosensitive layer. When the remaining amount of the photosensitive layer is to be regarded as an AC impedance, it is necessary to make it possible for electricity to flow, such as by contact between the PS plate and the electrode, or through a liquid that is an electrolyte between the PS plate electrodes. is there.
また、一方の電極がPS版と接触し、もう一方の電極がPS
版との間に電解質である液体を介して離れていてもよ
い。いずれにせよPS版と電極との間に電気が流れ得る状
態にしておく必要がある。Also, one electrode is in contact with the PS plate and the other electrode is PS
It may be separated from the plate through a liquid which is an electrolyte. In any case, it is necessary to make it possible for electricity to flow between the PS plate and the electrode.
本発明において、非画像部感光層の溶出度合に応じて現
像補充液を補充するには、溶出度合に対応する測定値と
該測定値に対応する適切な補充量との関係を予め実験等
によって求めておき、それに基づいて補充量を決めれば
よい。上記適切な補充量は溶出度合に対応する測定値が
新液における測定値を維持するように求めればよい。In the present invention, in order to replenish the developing replenisher according to the elution degree of the non-image area photosensitive layer, the relationship between the measured value corresponding to the elution degree and the appropriate replenishment amount corresponding to the measured value is previously determined by experiments or the like. It is only necessary to determine the amount of replenishment based on the demand. The appropriate replenishment amount may be determined so that the measured value corresponding to the elution degree maintains the measured value in the new solution.
本発明の方法における品種の識別、PS版の非画像部感光
層の溶出度合の測定および現像補充液の補充条件の関係
は、例えば露光済みのPS版を現像処理するときに品種識
別センサーにより該PS版の品種を識別し、識別した該品
種で予め定めておいた溶出度合の設定値と処理されてい
る該品種のPS版の溶出度合とが一致したときに該溶出度
合の設定値に対応した量の現像補充液が補充されるよう
にする。The relationship between the type identification in the method of the present invention, the measurement of the elution degree of the non-image area photosensitive layer of the PS plate and the replenishment condition of the developing replenisher is, for example, by the type identification sensor when developing the exposed PS plate. Identifies the PS version varieties, and responds to the set value of the elution degree when the preset elution degree set value for the identified variety and the PS version elution degree of the processed variety match Make sure that the specified amount of development replenisher is replenished.
このときの溶出度合の設定値は一段でもよく、また多段
でもよい。設置値が一段の場合には、溶出度合が対応す
る品種に対して定めた一定値以下になったとき一定量の
現像補充液が補充されるようになる。一方、設定値が多
段の場合は、溶出度合の測定値が対応する品種に対して
予め定めておいた各段の設置値のいずれかに一致する
と、一致した段数に対応する予め定まった一定量の現像
補充液を補充する。The set value of the elution degree at this time may be one step or multistep. When the set value is one step, a certain amount of the developer replenisher is replenished when the elution degree becomes less than the certain value determined for the corresponding product type. On the other hand, when the set value is multi-step, if the measured value of the elution degree matches any of the preset values of each step set for the corresponding varieties, a predetermined fixed amount corresponding to the number of matched steps. Replenish the developer replenisher.
本発明においては、上記の如き一連の制御情報を各PS版
品種ごとに予め入力しておき、識別された品種に対応し
て制御処理がなされている。In the present invention, the series of control information as described above is input in advance for each PS version type, and the control process is performed corresponding to the identified type.
上記以外の補充方法としては、例えば品種識別センサー
により品種を識別し、溶出度合を表わす測定値が品種に
関係なく一定の設定値を示したときに品種ごとに予め定
められた量の現像補充液を補充する。この時も前述の方
法と同様じ溶出度合の設定値は一段でも多段でもよい。As a replenishment method other than the above, for example, when a product type is identified by a product type identification sensor and the measured value indicating the elution degree shows a constant set value regardless of the product type, a predetermined amount of the developer replenisher solution To replenish. Also at this time, the set value of the elution degree may be one step or multiple steps as in the above method.
すなわち品種に関係なく一定の設定値を一段あるいは多
段設け、品種に関係なく溶出度合が予め定めた設定値に
一致すると、その設定値に対して品種ごとに予め定めら
れた量の現像補充液を補充する。That is, a fixed set value is provided regardless of product type in one step or multiple steps, and when the elution degree matches a predetermined set value regardless of product type, a predetermined amount of development replenisher liquid is applied to the set value for each product type. refill.
本発明ではこれらの制御情報は、補充装置に予め入力し
ておく。この入力は使用者がキーボードから入力しても
よいし、あるいは予め入力された制御板を補充装置に組
み込んでおいてもよい。また品種の識別に磁気カードな
どの中間媒体を使用する場合は、その中間媒体に制御情
報を入力しておいて、その制御情報に基づいて補充を行
なってもよい。In the present invention, such control information is input in advance in the replenishing device. This input may be input by the user from the keyboard, or a previously input control plate may be incorporated in the replenishing device. When an intermediate medium such as a magnetic card is used to identify the product type, control information may be input to the intermediate medium and supplementation may be performed based on the control information.
本発明において、補充する現像補充液の量は補充する現
像補充液の活性度により異なるが、1回の補充量は現像
液の仕込母液量40l当り101以下が好ましく、より好まし
くは仕込母液量40l当り4l以下である。In the present invention, the amount of the developing replenisher to be replenished depends on the activity of the developing replenisher to be replenished, but the replenishment amount per time is preferably 101 or less per 40 l of the mother liquor of the developer charged, and more preferably 40 l It is less than 4l.
本発明に係る補充方法に併せて、外気温度の変化やシャ
ワー流速の変化などによる空気中の炭酸ガスの吸収度合
の変化を検知し、それに伴って変化する空気中の炭酸ガ
スの吸収による疲労に対応する量の補充液を補充し、PS
版の処理の有無にかかわらず現像液活性を常に一定に保
つようにすることが望ましい。Along with the replenishment method according to the present invention, a change in the degree of absorption of carbon dioxide in the air due to a change in the outside air temperature, a change in the shower flow velocity, etc. is detected, and fatigue due to the absorption of carbon dioxide in the air that changes accordingly is detected. Replenish the corresponding amount of replenisher with PS
It is desirable to always keep the developer activity constant regardless of whether the plate is processed or not.
実施例 以下、実施例で本発明を更に具体的に説明する。Examples Hereinafter, the present invention will be described in more detail with reference to Examples.
実施例1 ポジ型PS版FPS-A及びFPP(富士写真フィルム株式会社)
の1003mm×800mmの大きさものを多数枚用意し、これら
に透明陽画を通して80cmの距離から2kWのメタルハイド
ランプを用いて70秒間露光した。一方、SDR-1(小西六
写真工業株式会社)を水で6倍希釈し調製した現像液及
びSDR-1R(小西六写真工業株式会社)を水で4倍希釈し
調製した現像補充液を用意した。Example 1 Positive PS version FPS-A and FPP (Fuji Photo Film Co., Ltd.)
A large number of 1003 mm × 800 mm size specimens were prepared and exposed through a transparent positive image from a distance of 80 cm for 70 seconds using a 2 kW metal hydrate lamp. On the other hand, prepare a developer prepared by diluting SDR-1 (Konishi Roku Photo Industry Co., Ltd.) 6 times with water and a developer replenisher prepared by diluting SDR-1R (Konishi Roku Photo Industry Co., Ltd.) 4 times with water. did.
前記露光済みのPS版を前記現像液及び現像補充液を用
い、第1図に示す自動現像機を用いて処理を行った。第
1図において、1は現像槽、2は搬送ローラ、3は絞り
ローラ、6はブラシローラ、12はPS版の非画像部に残存
する感光層の量を測定する光反射センサー、13は現像液
除去ローラである。ポンプ7から送られる現像液はシャ
ワーパイプ8,8′,8″および8からPS版上に供給され
る。光反射センサー12の設置位置は受光面が搬送される
PS版上10mmの位置になるように決め、さらに入り口にあ
る搬送ローラ2から全現像ゾーンの1/5の位置になるよ
うに決めた。現像液除去ローラ13で、現像ゾーンの途中
で現像液を一時的に除去し、PS版の非画像部に残存する
感光層の量を光反射センサー12で測定できるようにし
た。The exposed PS plate was processed using the developing solution and the developing replenisher using the automatic developing machine shown in FIG. In FIG. 1, 1 is a developing tank, 2 is a conveying roller, 3 is a squeezing roller, 6 is a brush roller, 12 is a light reflection sensor for measuring the amount of the photosensitive layer remaining in the non-image portion of the PS plate, and 13 is a developing device. It is a liquid removal roller. The developer sent from the pump 7 is supplied onto the PS plate from the shower pipes 8, 8 ', 8 "and 8. The light receiving surface is transported to the installation position of the light reflection sensor 12.
It was decided to be at a position of 10 mm on the PS plate, and further to be at a position 1/5 of the entire development zone from the transport roller 2 at the entrance. The developing solution removing roller 13 temporarily removed the developing solution in the middle of the developing zone, and the light reflection sensor 12 could measure the amount of the photosensitive layer remaining in the non-image area of the PS plate.
光反射センサー12の信号は、制御装置10′で出力電圧に
変換され処理され、その値によってPS版の品種を識別
し、同時にその値に応じて補充装置11′を作動させ、あ
る所定量の補充液が補充されるようにした。The signal of the light reflection sensor 12 is converted into an output voltage by the control device 10 'and processed, the PS plate type is identified by the value, and at the same time, the replenishing device 11' is operated in accordance with the value, and a predetermined amount of The replenisher was replenished.
光反射センサーの信号の処理値と品種の識別の関係は処
理値が0.30以下の時は、FPS-Aと判定し、0.30より大き
い値の時はFPD-Aと判定するようにした。さらに識別さ
れた品種と処理値と現像補充液量の関係は表1のように
設定した。表1においてxは光反射センサーの信号の処
理値を示す。Regarding the relationship between the processed value of the light reflection sensor signal and the identification of the product type, when the processed value is 0.30 or less, it is determined as FPS-A, and when the processed value is greater than 0.30, it is determined as FPD-A. Further, the relationship between the identified product type, the processing value, and the developing replenisher amount was set as shown in Table 1. In Table 1, x indicates a processed value of the signal of the light reflection sensor.
また自動現像機の作動中はPS版の処理とは無関係に1時
間毎に35mlの現像補充液が補充され、自動現像機の作動
を休止した場合は15時間につき300mlの現像補充液が補
充されるようにした。 In addition, while the automatic processor is operating, 35 ml of development replenisher is replenished every hour regardless of PS plate processing, and when the automatic processor is stopped, 300 ml of development replenisher is replenished every 15 hours. It was to so.
現像液タンク1′に前記現像液を401仕込み、搬送ロー
ラ2の速度を全現像時間が40秒間になるように設定し、
また現像液温を25℃に設定して前記露光済みのPS版の処
理を行った。1枚目の露光済みのPS版FPS-Aを処理した
時、光反射センサーにPS版が達した時点で測定部分の感
光層は、ほぼ溶出しており、光反射センサーの信号の処
理値は0.21を示した。401 is charged with the developing solution in the developing solution tank 1 ', the speed of the conveying roller 2 is set so that the total developing time is 40 seconds,
Further, the developing solution temperature was set to 25 ° C. and the exposed PS plate was processed. When the first exposed PS plate FPS-A was processed, when the PS plate reached the light reflection sensor, the photosensitive layer in the measurement area was almost eluted, and the processed value of the light reflection sensor signal was It showed 0.21.
次に露光済みのPS版FPD-Aを処理したところ、上記セン
サーにPS版が達した時点で測定部分の感光層は、ほぼ溶
出しており、処理値は0.31を示した。引き続き露光済み
のPS版FPS-A及びFPD-Aを処理して合計20枚処理した。FP
S-A及びFPD-Aの処理は順不同で行った。次に21枚目の露
光済みのPS版FPS-Aを処理したところ、処理値は0.24を
示し、自動的に420mlの現像補充液が補充された。続い
て22枚目の露光済みのPS版FPD-Aを処理すると、処理値
は再び0.31を示した。さらに処理を続け45枚目に露光済
みのPS版FPD-Aを処理したところ、処理値は0.34を示
し、自動的に420mlの現像補充液が補充された。続いて4
6枚目の露光済みのPS版FPS-Aを処理すると処理値は再び
0.21を示した。Next, when the exposed PS plate FPD-A was processed, when the PS plate reached the sensor, the photosensitive layer in the measurement portion was almost eluted, and the processed value was 0.31. Subsequently, the exposed PS plates FPS-A and FPD-A were processed to process 20 sheets in total. FP
The SA and FPD-A treatments were performed in any order. When the 21st exposed PS plate FPS-A was processed, the processed value was 0.24, and 420 ml of the development replenisher was automatically replenished. Subsequently, when the 22nd exposed PS plate FPD-A was processed, the processed value was 0.31 again. When the 45th sheet of exposed PS plate FPD-A was processed further, the processed value was 0.34, and 420 ml of the developing replenisher was automatically replenished. Then 4
When the 6th exposed PS plate FPS-A is processed, the processed value is again
It showed 0.21.
このようにして露光済みのPS版FPS-A及びFPD-Aを合計約
1000枚処理したところ、すべて新液で処理したものとほ
ぼ同一の感度を示し、かつ安定な網点再現性を有する平
版印刷版が得られた。In this way, the exposed PS plates FPS-A and FPD-A total about
When 1000 sheets were processed, a lithographic printing plate which showed almost the same sensitivity as the one treated with the new solution and had stable halftone dot reproducibility was obtained.
比較例1 実施例1で用いたPS版、現像液、現像補充液および自動
現像機を用いて露光済みのPS版を処理した。但し光反射
センサーの信号の処理値と補充液量の関係は、処理値が
0.34以上の値を示した時にのみ420mlの現像補充液が補
充されるようにした。処理値と補充の関係以外は、すべ
て実施例2と同様に設定し、露光済みのPS版FPS-A及びF
PD-Aを合計約1000枚処理したところ、感度が大きくばら
ついた。特に露光済みのPS版FPS-Aを数十枚連続して処
理した場合、その間補充は全く行われず、感度の低下は
非常に著しいものであった。Comparative Example 1 The exposed PS plate was processed using the PS plate, the developing solution, the developing replenisher and the automatic developing machine used in Example 1. However, the relationship between the processed value of the light reflection sensor signal and the amount of replenisher is
Only when the value was 0.34 or more, 420 ml of the developing replenisher was replenished. Except for the relationship between the processed value and the replenishment, all the PS plates FPS-A and F which have been exposed and set in the same manner as in Example 2
When a total of about 1000 PD-A's were processed, the sensitivity varied greatly. In particular, when several tens of exposed PS plates FPS-A were processed continuously, replenishment was not performed at all during that time, and the decrease in sensitivity was extremely remarkable.
比較例2 実施例1で用いたPS版、現像液及び現像補充液を用いて
露光済みのPS版を処理した。ただし、自動現像機として
は第2図に示すものを用いた。Comparative Example 2 The exposed PS plate was treated with the PS plate, the developing solution and the developing replenisher used in Example 1. However, the automatic developing machine shown in FIG. 2 was used.
第2図において、1は現像槽、2は搬送ローラ、3は絞
りローラ、4は串ローラ、5は受ローラ、6はブラシロ
ーラである。ポンプ7から送られる現像液はシャワーパ
イプ8,8′,8″および8からPS版上に供給される。9,
9′はステンレス製の電極板で、その大きさは厚さ1mmの
1cm×2cmである。その設置位置は搬送されるPS版の3mm
上方で、該PS版の幅方向の左端から5mmの位置であり、
その位置は常に非画像部が通過するようにした。また搬
送ローラ2の速度を全現像時間が40秒間になるように設
定した。また現像液温は25℃に設定した。電極板9と
9′はその中心間の距離が10cmになるようにした。10は
交流インピーダンス計と、それに接続した制御スイッチ
であり、10kHzの定電流を被測定物に流し、被測定物の
インピーダンスを測定した。In FIG. 2, 1 is a developing tank, 2 is a conveying roller, 3 is a squeezing roller, 4 is a skewer roller, 5 is a receiving roller, and 6 is a brush roller. The developer sent from the pump 7 is supplied onto the PS plate from the shower pipes 8, 8 ', 8 "and 8.
9'is an electrode plate made of stainless steel, the size of which is 1 mm thick
It is 1 cm x 2 cm. The installation position is 3 mm for the PS plate being transported.
Above, at a position 5 mm from the left end in the width direction of the PS plate,
The non-image part always passes through the position. The speed of the transport roller 2 was set so that the total developing time was 40 seconds. The developer temperature was set to 25 ° C. The distance between the centers of the electrode plates 9 and 9'is 10 cm. Reference numeral 10 is an AC impedance meter and a control switch connected to the AC impedance meter. A constant current of 10 kHz was passed through the measured object to measure the impedance of the measured object.
そして、交流インピーダンス計10で測定したインピーダ
ンス値と補充液量の関係を、インピーダンス値が26Ω以
上の値を示した時にのみ420mlの現像補充液が補充され
るようにした。このようにして、露光済みのPS版を合計
約1000枚処理したところ、感度が大きくばらついた。特
に露光済みのPS版FPPを数十枚連続して処理した場合、
その間補充は全く行われず、感度の低下は非常に激しい
ものであった。The relationship between the impedance value measured by the AC impedance meter 10 and the amount of the replenisher solution was set so that the development replenisher solution of 420 ml was replenished only when the impedance value showed a value of 26Ω or more. In this way, when a total of about 1000 exposed PS plates were processed, the sensitivity greatly varied. Especially when dozens of exposed PS plates FPP are processed continuously,
During that time, replenishment was not performed at all, and the decrease in sensitivity was extremely severe.
(発明の効果) 現像処理される感光性平版印刷版の非画像部感光層の少
なくとも一部分の溶出度合を測定し、その溶出度合に応
じて現像補充液を補充する処理方法において、上記印刷
版の品種を検知し、予め入力されている該印刷版の補充
条件と対比せしめ算定された補充条件に従って現像補充
液を補充する如くなしたので品種の異なる前記印刷版を
現像処理する場合にも現像液の液活性を常に安定して維
持することができる。処理後、感度低下のない良好な網
点性能を有する印刷版を得ることができる。(Effect of the invention) In the processing method of measuring the dissolution degree of at least a part of the non-image area photosensitive layer of the photosensitive lithographic printing plate to be developed, and replenishing the developing replenisher according to the dissolution degree, The developing replenisher is replenished according to the replenishing conditions calculated by comparing the replenishing conditions of the printing plate which are input in advance, so that the developing solution can be used even when developing printing plates of different types. The liquid activity of can be always maintained stable. After the treatment, it is possible to obtain a printing plate having good halftone dot performance without sensitivity deterioration.
第1図は本発明に用いられる自動現像機の1例を示す概
要構成図、また第2図は同上装置の他の実施例を示す概
要構成図である。 1……現像槽、1′……現像液タンク、9,9′……電極
板、10……制御スイッチ、10′……制御装置、 11,11′……補充装置、12……光反射センサーFIG. 1 is a schematic configuration diagram showing an example of an automatic developing machine used in the present invention, and FIG. 2 is a schematic configuration diagram showing another embodiment of the same apparatus. 1 ... development tank, 1 '... developer tank, 9,9' ... electrode plate, 10 ... control switch, 10 '... control device, 11,11' ... replenishment device, 12 ... light reflection sensor
───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭60−194446(JP,A) 特開 昭58−95349(JP,A) 特開 昭58−27144(JP,A) ─────────────────────────────────────────────────── ─── Continuation of the front page (56) Reference JP-A-60-194446 (JP, A) JP-A-58-95349 (JP, A) JP-A-58-27144 (JP, A)
Claims (1)
用いて露光済み感光性平版印刷版を自動的に搬送、現像
処理し、かつ感光性平版印刷版の非画像部感光層の少な
くとも一部分の溶出度合を測定し、その測定した溶出度
合に応じて現像補充液を補充する感光性平版印刷版の処
理方法において、上記感光性平版印刷版の品種を検知
し、感光性平版印刷版の品種に応じて予め複数入力して
おいた補充条件と対比せしめ、該補充条件に従って現像
補充液を補充することを特徴とする感光性平版印刷版の
処理方法。ただし、上記感光性平版印刷版の品種を検知
する手段がインピーダンス値の測定によるものである場
合を除く。1. An exposed photosensitive lithographic printing plate is automatically conveyed and developed by using an automatic processor having a developing replenisher replenishing device, and at least a part of a non-image area photosensitive layer of the photosensitive lithographic printing plate. In the method for processing a photosensitive lithographic printing plate in which the elution degree of is measured and the developing replenisher is replenished according to the measured elution degree, the type of the photosensitive lithographic printing plate is detected, and the type of the photosensitive lithographic printing plate is detected. A method for processing a photosensitive lithographic printing plate, which comprises comparing the replenishment conditions input in advance according to the above conditions and replenishing the development replenisher according to the replenishment conditions. However, the case where the means for detecting the type of the photosensitive lithographic printing plate is by measuring the impedance value is excluded.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59240146A JPH0675192B2 (en) | 1984-11-13 | 1984-11-13 | Photosensitive lithographic printing plate processing method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59240146A JPH0675192B2 (en) | 1984-11-13 | 1984-11-13 | Photosensitive lithographic printing plate processing method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61117547A JPS61117547A (en) | 1986-06-04 |
JPH0675192B2 true JPH0675192B2 (en) | 1994-09-21 |
Family
ID=17055176
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59240146A Expired - Lifetime JPH0675192B2 (en) | 1984-11-13 | 1984-11-13 | Photosensitive lithographic printing plate processing method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0675192B2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63186247A (en) * | 1987-01-28 | 1988-08-01 | Konica Corp | Processing method for photosensitive material |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0312310A (en) * | 1989-06-07 | 1991-01-21 | Nippon Valqua Ind Ltd | Superconducting material and its production |
-
1984
- 1984-11-13 JP JP59240146A patent/JPH0675192B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPS61117547A (en) | 1986-06-04 |
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