JPH021389A - Thermal recording type planographic original plate material - Google Patents
Thermal recording type planographic original plate materialInfo
- Publication number
- JPH021389A JPH021389A JP63142647A JP14264788A JPH021389A JP H021389 A JPH021389 A JP H021389A JP 63142647 A JP63142647 A JP 63142647A JP 14264788 A JP14264788 A JP 14264788A JP H021389 A JPH021389 A JP H021389A
- Authority
- JP
- Japan
- Prior art keywords
- heat
- thermal
- printing
- original plate
- binder
- 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
- 239000000463 material Substances 0.000 title abstract description 5
- 238000007639 printing Methods 0.000 claims abstract description 43
- 239000011230 binding agent Substances 0.000 claims abstract description 21
- 239000000126 substance Substances 0.000 claims abstract description 20
- 239000000945 filler Substances 0.000 claims abstract description 11
- 229920003023 plastic Polymers 0.000 claims abstract description 11
- 239000004033 plastic Substances 0.000 claims abstract description 11
- 239000001023 inorganic pigment Substances 0.000 claims abstract description 9
- 238000002844 melting Methods 0.000 claims description 17
- 239000011796 hollow space material Substances 0.000 claims 1
- 238000007651 thermal printing Methods 0.000 abstract description 13
- 230000015572 biosynthetic process Effects 0.000 abstract description 4
- 230000008542 thermal sensitivity Effects 0.000 abstract description 3
- 238000000034 method Methods 0.000 description 24
- 239000001993 wax Substances 0.000 description 11
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 10
- 229920001577 copolymer Polymers 0.000 description 10
- 239000011248 coating agent Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 8
- -1 polyethylene Polymers 0.000 description 8
- 229920005989 resin Polymers 0.000 description 8
- 239000011347 resin Substances 0.000 description 8
- 239000004372 Polyvinyl alcohol Substances 0.000 description 7
- 239000000976 ink Substances 0.000 description 7
- 229920002451 polyvinyl alcohol Polymers 0.000 description 7
- 239000007788 liquid Substances 0.000 description 5
- 239000011787 zinc oxide Substances 0.000 description 5
- 239000006185 dispersion Substances 0.000 description 4
- 238000005530 etching Methods 0.000 description 4
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 4
- 238000007645 offset printing Methods 0.000 description 4
- 229920000877 Melamine resin Polymers 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- 235000021355 Stearic acid Nutrition 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 3
- 239000012188 paraffin wax Substances 0.000 description 3
- 229920006122 polyamide resin Polymers 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 239000002952 polymeric resin Substances 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000008117 stearic acid Substances 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 150000001447 alkali salts Chemical class 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 235000013871 bee wax Nutrition 0.000 description 2
- 239000012166 beeswax Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000004204 candelilla wax Substances 0.000 description 2
- 235000013868 candelilla wax Nutrition 0.000 description 2
- 229940073532 candelilla wax Drugs 0.000 description 2
- 239000004203 carnauba wax Substances 0.000 description 2
- 235000013869 carnauba wax Nutrition 0.000 description 2
- 239000012185 ceresin wax Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 229940015043 glyoxal Drugs 0.000 description 2
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 2
- 230000005660 hydrophilic surface Effects 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000004200 microcrystalline wax Substances 0.000 description 2
- 235000019808 microcrystalline wax Nutrition 0.000 description 2
- 239000012170 montan wax Substances 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000012176 shellac wax Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- 229920003169 water-soluble polymer Polymers 0.000 description 2
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N 1,1-Diethoxyethane Chemical compound CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- QLUXVUVEVXYICG-UHFFFAOYSA-N 1,1-dichloroethene;prop-2-enenitrile Chemical compound C=CC#N.ClC(Cl)=C QLUXVUVEVXYICG-UHFFFAOYSA-N 0.000 description 1
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-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
- DXIJHCSGLOHNES-UHFFFAOYSA-N 3,3-dimethylbut-1-enylbenzene Chemical compound CC(C)(C)C=CC1=CC=CC=C1 DXIJHCSGLOHNES-UHFFFAOYSA-N 0.000 description 1
- HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 229920012753 Ethylene Ionomers Polymers 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- 229920001890 Novodur Polymers 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- 239000011354 acetal resin Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 229940037003 alum Drugs 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- AYJRCSIUFZENHW-DEQYMQKBSA-L barium(2+);oxomethanediolate Chemical compound [Ba+2].[O-][14C]([O-])=O AYJRCSIUFZENHW-DEQYMQKBSA-L 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 229940100242 glycol stearate Drugs 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000001282 iso-butane Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000011859 microparticle Substances 0.000 description 1
- 239000004005 microsphere Substances 0.000 description 1
- KINULKKPVJYRON-PVNXHVEDSA-N n-[(e)-[10-[(e)-(4,5-dihydro-1h-imidazol-2-ylhydrazinylidene)methyl]anthracen-9-yl]methylideneamino]-4,5-dihydro-1h-imidazol-2-amine;hydron;dichloride Chemical compound Cl.Cl.N1CCN=C1N\N=C\C(C1=CC=CC=C11)=C(C=CC=C2)C2=C1\C=N\NC1=NCCN1 KINULKKPVJYRON-PVNXHVEDSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920002102 polyvinyl toluene Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920006027 ternary co-polymer Polymers 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000013053 water resistant agent Substances 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Landscapes
- Printing Plates And Materials Therefor (AREA)
- Manufacture Or Reproduction Of Printing Formes (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、感熱記録型平版印刷用原版の改良に関し、更
に詳しくは、光源及び現像定着等の処理を必要とせず、
熱印字装置により容易に記録できる感熱記録型平版印刷
用原版に関する。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to an improvement of a heat-sensitive recording type lithographic printing original plate, and more specifically, the present invention relates to an improvement of a heat-sensitive recording type lithographic printing original plate, which does not require a light source and processing such as development and fixation.
The present invention relates to a thermal recording type lithographic printing original plate that can be easily recorded using a thermal printing device.
平版印刷原版の作成方法としては、(1)親水性表面を
有する支持体上にインクジェットを適用する方法(特開
昭51−84303号、特開昭56−6215号。Methods for preparing a lithographic printing original plate include (1) a method of applying inkjet onto a support having a hydrophilic surface (Japanese Patent Application Laid-open Nos. 51-84303 and 1982-6215);
特開昭56−113456号)(2)親水性表面を有す
る支持体を用いワイヤートッド式や熱転写により製版す
る方法(特開昭58−193154号、特開昭59−7
6260号)(3)有機光導電体を使用するもの(特開
昭60−239762号)(4)フタロシアニンと酸化
亜鉛の分散系を使用したもの(特開昭60−24010
60号)(5)放電破壊により製版するもの(特開昭5
4−6602号、特開昭50−59113号、特開昭6
0−194467号)(6)レーザー光で親水層を疎水
層を除去する方法(特開昭50−113307号)やヒ
ートモードで製版する方法(特開昭50−158405
号)等が知られている。JP-A-56-113-456) (2) A method of plate making by wire tod method or thermal transfer using a support having a hydrophilic surface (JP-A-58-193-154, JP-A-59-7)
6260) (3) Those using an organic photoconductor (JP-A No. 60-239762) (4) Those using a dispersion system of phthalocyanine and zinc oxide (JP-A No. 60-24010)
No. 60) (5) Plate making by discharge destruction (Unexamined Japanese Patent Publication No. 1973)
No. 4-6602, JP-A No. 50-59113, JP-A No. 6
0-194467) (6) A method of removing a hydrophilic layer and a hydrophobic layer with a laser beam (Japanese Patent Application Laid-Open No. 113307-1982) and a method of plate making in heat mode (Japanese Patent Application Laid-open No. 158405-1982)
No.) etc. are known.
しかしながら、これらの方法は、いずれも種々の問題を
包含し工業的に満足すべき方法ではなかった。例えば、
(1)及び(2)の方法は、特殊なインキや転写リボン
を用いなければならず、また(3)及び(4)の方法に
おいては親水化するための洗浄工程を必要とする主電子
写真プロセスを利用するために、現像(トナー)工程を
も必要とするもので、製版コストが高くなり、また感度
も低いという欠点を有する。更に、(5)の放電破壊を
利用する方法は電極針の摩耗が著しく、工業的に有利な
製造法ということはできず、また(6)の方法は装置が
大型化し、事務用印刷には不向きである。However, all of these methods involve various problems and are not industrially satisfactory. for example,
Methods (1) and (2) require the use of special inks and transfer ribbons, and methods (3) and (4) require a cleaning process to make them hydrophilic. In order to utilize the process, a developing (toner) step is also required, which has the drawbacks of high plate-making cost and low sensitivity. Furthermore, the method (5) that uses discharge breakdown causes significant wear on the electrode needles and cannot be considered an industrially advantageous manufacturing method, and the method (6) requires larger equipment and is not suitable for office printing. Not suitable.
ところで、最近、これら従来の平版印刷用原版の製造法
の欠点を解消する方法として、サーマルヘッド等の熱印
字装置を用いる方法が提案されている(特開昭58−1
99153号、特開昭59−174395号)。By the way, recently, a method using a thermal printing device such as a thermal head has been proposed as a method to overcome the drawbacks of these conventional methods of manufacturing lithographic printing original plates (Japanese Patent Laid-Open No. 58-1
No. 99153, JP-A-59-174395).
これらの方法は、耐水性支持体上に、融点60〜180
℃かつ粒径0.1〜10癖のワックス、ポリビニルアル
コールあるいはアセトアセチル化ポリビニルアルコール
等の親水性バインダー及び顔料等を含む感熱記録層を設
けた平版印刷用原版を用い、該感熱記録層面をサーマル
ヘッドで熱印字することによりオフセット刷版を製造す
るものであり、従来のように光源や現像定着を必要とせ
ず簡単な装置でオフセット刷版が得られるという利点を
有する。These methods are used to prepare a material with a melting point of 60 to 180 on a water-resistant support.
Using a lithographic printing original plate provided with a heat-sensitive recording layer containing a wax, a hydrophilic binder such as polyvinyl alcohol or acetoacetylated polyvinyl alcohol, and a pigment with a particle size of 0.1 to 10 °C, the surface of the heat-sensitive recording layer is thermally heated. An offset printing plate is manufactured by thermal printing with a head, and has the advantage that an offset printing plate can be obtained with a simple device without requiring a light source or developing and fixing as in the past.
しかしながら、かかる方法は、熱印字を行う層に、ポリ
ビニルアルコールやアセトアセチル化ボリビジルアルコ
ール等の親水性樹脂を含有する平版印刷用原版を用いて
いるために、熱印字する際にスティッキングを生じると
共に熱印字層(記録層)に充分な親油性を付与すること
ができず、このため、これらのオフセット刷版で印刷し
た印刷物の画像濃度が低くなり、また、画像ムラを生じ
るという問題を惹起し、鮮明な印刷画像が得られないと
いう欠点があった。However, since this method uses a lithographic printing original plate containing a hydrophilic resin such as polyvinyl alcohol or acetoacetylated boribidyl alcohol in the thermal printing layer, sticking occurs during thermal printing and It is not possible to impart sufficient lipophilicity to the thermal printing layer (recording layer), which causes problems such as low image density and uneven images in printed matter printed with these offset printing plates. However, there was a drawback that clear printed images could not be obtained.
本発明は、画像濃度に優れると共に画像ムラがなく、か
つ地汚れのない鮮明な印刷画像を与え、しかもサーマル
ヘッドへのスティッキングが生じない感熱記録型平版印
刷用原版を提供することを目的とする。SUMMARY OF THE INVENTION An object of the present invention is to provide a heat-sensitive recording type lithographic printing original plate that has excellent image density, provides a clear printed image without image unevenness, and has no background smear, and does not cause sticking to a thermal head. .
本発明によれば、支持体上に無機顔料、結着剤及び熱溶
融性物質を主成分とする感熱記録層を設けた感熱記録型
平版印刷用原版において、支持体と感熱記録層との間に
中空状プラスチックフィラ、熱溶融物質及び結着剤とか
ら成る中間層を設けたことを特徴とする感熱記録型平版
印刷用原版が提供される。According to the present invention, in a heat-sensitive recording type lithographic printing original plate in which a heat-sensitive recording layer mainly composed of an inorganic pigment, a binder, and a heat-melting substance is provided on a support, there is a gap between the support and the heat-sensitive recording layer. Provided is a heat-sensitive recording type lithographic printing original plate, characterized in that an intermediate layer comprising a hollow plastic filler, a heat-melting substance, and a binder is provided.
本発明の感熱記録型平版印刷用原版は、支持体と感熱記
録層との前記した特定の中間層を設けたことから熱印字
する際にサーマルヘッドへのスティッキングもなく良好
な印字画像を与え、またこのものから得られる平版印刷
用刷版を用いて印刷すると、画像濃度に優れると共に解
像力に優れ、しかも地汚れのない鮮明な印刷画像を有す
る印刷物を得ることができる。Since the heat-sensitive recording type lithographic printing original plate of the present invention is provided with the above-mentioned specific intermediate layer between the support and the heat-sensitive recording layer, it provides a good printed image without sticking to the thermal head during thermal printing. Further, when printing using a lithographic printing plate obtained from this product, it is possible to obtain printed matter having excellent image density and resolution, and having a clear printed image without background smearing.
以下、本発明を更に詳細に説明する。The present invention will be explained in more detail below.
本発明において中間層に含有させる中空状プラスチック
フィラーとしては、熱可塑性樹脂を殻とし、内部に低沸
点溶媒を含有するフィラーが用いられる。In the present invention, as the hollow plastic filler contained in the intermediate layer, a filler having a thermoplastic resin shell and containing a low boiling point solvent inside is used.
このプラスチック微小粒子の殻となる熱可塑性樹脂とし
ては、ポリスチレン、ポリ塩化ビニル、ポリ塩化ビニリ
デン、ポリ酢酸ビニル、ポリアクリル酸エステル、ポリ
アクリロニトリル、ポリブタジェン、あるいはそれらの
共重合体、例えば塩化ビニリデン−アクリロニトリル共
重合体が挙げられる。また殻内に含まれる低沸点溶媒(
発泡剤)としては、プロパンやブタン、イソブタン等が
一般的である。The thermoplastic resin that forms the shell of the plastic microparticles may be polystyrene, polyvinyl chloride, polyvinylidene chloride, polyvinyl acetate, polyacrylate, polyacrylonitrile, polybutadiene, or a copolymer thereof, such as vinylidene chloride-acrylonitrile. Examples include copolymers. Also, the low boiling point solvent contained within the shell (
As the foaming agent, propane, butane, isobutane, etc. are generally used.
本発明で用いられるプラスチックフィラーとしては、例
えば日本フェライト社製ADCA、 AlB111、D
PT、0BSH,TSI+や松本油脂社製のF−30、
F−50等が挙げられる。Examples of the plastic filler used in the present invention include ADCA, AlB111, and D manufactured by Nippon Ferrite Co., Ltd.
PT, 0BSH, TSI+ and F-30 manufactured by Matsumoto Yushi Co., Ltd.
Examples include F-50.
熱溶融物質としては50℃〜200℃で溶融するものが
好ましく使用され、このような熱溶融性物質としては、
たとえば、カルナバワックス、オーリキュリーワックス
、マイクロクリスタリンワックス、パラフィンワックス
、セレシンワックス、モンタンワックス、キャンデリラ
ワックス、セラックろう、チュウハクろう、密ろう、本
ろう、低分子量ポリエチレン、ステアリン酸等の脂肪酸
、ポリエチレングリコールステアレート等のワックス類
が挙げられる。As the heat-melting substance, those that melt at 50°C to 200°C are preferably used, and such heat-melting substances include:
For example, carnauba wax, auriculie wax, microcrystalline wax, paraffin wax, ceresin wax, montan wax, candelilla wax, shellac wax, wax wax, beeswax, real wax, low molecular weight polyethylene, fatty acids such as stearic acid, polyethylene glycol Examples include waxes such as stearate.
結着剤としては、従来公知のものが任意に使用され、水
溶性高分子樹脂や水分散型高分子樹脂が好ましく使用さ
れる。この場合、水溶性高分子樹脂としては例えば、ポ
リビニルアルコール、デンプン及びその誘導体、メトキ
シセルロース、ヒドロキシエチルセルロース、カルボキ
シメチルセルロース、メチルセルロース、エチルセルロ
ース等のセルロース誘導体、ポリアクリル酸ソーダ、ポ
リビニルピロリドン、アクリル酸アミド/アクリル酸エ
ステル共重合体、アクリル酸アミド/アクリル酸エステ
ル/メタクリル酸3元共重合体、スチレン/無水マレイ
ン酸共重合体アリカリ塩、イソブチレン/無水マレイン
酸共重合体アリカリ塩、ポリアクリルアミド、アルギン
酸ソーダ、ゼラチン、カゼイン等が挙げられる。As the binder, any conventionally known binder may be used, and water-soluble polymer resins and water-dispersible polymer resins are preferably used. In this case, water-soluble polymer resins include, for example, polyvinyl alcohol, starch and its derivatives, cellulose derivatives such as methoxycellulose, hydroxyethylcellulose, carboxymethylcellulose, methylcellulose, and ethylcellulose, sodium polyacrylate, polyvinylpyrrolidone, and acrylic acid amide/acrylic acid. Acid ester copolymer, acrylic amide/acrylic ester/methacrylic acid ternary copolymer, styrene/maleic anhydride copolymer alkali salt, isobutylene/maleic anhydride copolymer alkali salt, polyacrylamide, sodium alginate, Examples include gelatin and casein.
前記樹脂と縮合あるいは架橋反応の如き反応をして附水
化させるためにはたとえば、ホルムアルデヒド、グリオ
キザール、クロム明ばん、メラミン、メラミン−ホルム
アルデヒド樹脂、ポリアミド樹脂、ポリアミド−エピク
ロルヒドリン樹脂等の耐水化剤を用いることもできる。In order to cause a reaction such as a condensation or crosslinking reaction with the resin to make it hydrated, a water-resistant agent such as formaldehyde, glyoxal, chromium alum, melamine, melamine-formaldehyde resin, polyamide resin, polyamide-epichlorohydrin resin, etc. is used. It can also be used.
また、水分散型樹脂としては例えば、アクリル酸、メタ
クリル酸等の不飽和カルボン酸樹脂、塩化ビニル樹脂、
SBR、メタクリル酸メチル−ブタジェン共重合体、ア
ルキッド樹脂、フェノール樹脂。Examples of water-dispersed resins include unsaturated carboxylic acid resins such as acrylic acid and methacrylic acid, vinyl chloride resins,
SBR, methyl methacrylate-butadiene copolymer, alkyd resin, phenolic resin.
エポキシ樹脂、エチレンアイオノマ−樹脂等が挙げられ
る。Examples include epoxy resins and ethylene ionomer resins.
この中間層に含有させる結着剤と中空状プラスチックフ
ィラーの使用割合は重量比で179〜9/1、好ましく
は1/2が適当である。The weight ratio of the binder and the hollow plastic filler contained in this intermediate layer is preferably 179 to 9/1, preferably 1/2.
この使用割合は179未満であると接着性が低下して耐
刷性能が劣化し、また9/1を超えると熱感度が低下し
て画像品質が劣化するので好ましくない。If the usage ratio is less than 179, adhesiveness will decrease and printing durability will deteriorate, and if it exceeds 9/1, thermal sensitivity will decrease and image quality will deteriorate, which is not preferable.
また、熱溶融性物質の添加量は中間層の総重量に対して
、0.5〜10重ff1石、好ましくは3〜8重量%で
ある。0.5重量%未満であると印刷濃度が不足し、ま
た10重量%を超えると印刷物の地汚れが発生するので
好ましくない。The amount of the heat-fusible substance added is 0.5 to 10% by weight, preferably 3 to 8% by weight, based on the total weight of the intermediate layer. If it is less than 0.5% by weight, the printing density will be insufficient, and if it exceeds 10% by weight, scumming will occur in the printed matter, which is not preferable.
中間層の支持体に対する付着量は、用いるプラスチック
フィラー、結着剤及び熱溶融性物質の種類によっても異
なるが、通常、乾燥重量で1〜15g/ボ、好ましくは
8〜12g/mである。The amount of the intermediate layer attached to the support varies depending on the type of plastic filler, binder, and heat-fusible substance used, but is usually 1 to 15 g/m, preferably 8 to 12 g/m in terms of dry weight.
本発明の感熱記録J−に使用する無機顔料としては、ク
レー、シリカ、酸化亜鉛、酸化チタン、酸化アルミニウ
ム、炭酸カルシウム、炭酸バリウム、硫酸バリウム等が
挙げられるが、効果の発現性あるいは使用感度の点から
みて酸化亜鉛を用いることが好ましい。Inorganic pigments used in the thermal recording J- of the present invention include clay, silica, zinc oxide, titanium oxide, aluminum oxide, calcium carbonate, barium carbonate, barium sulfate, etc. From this point of view, it is preferable to use zinc oxide.
また、結着剤としては、環球法による軟化点又は融点が
150℃以下のものが好ましく、このような結着剤の具
体例としては、たとえば、ポリスチレン、スチレン−ア
クリル蹟エステル共重合体、ポリ−t−ブチルスチレン
のようなスチレン系樹脂、低融点ポリアミド樹脂、ポリ
アクリル酸エステル、アクリル酸エステル/アクリル酸
エステル共重合体、ポリエステル樹脂、エチレン−酢酸
ビニル共重合体、塩化ビニル−酢酸ビニル共重合体、塩
化ビニリデン樹脂、ブチラール樹脂、アセタール樹脂、
ポリビニルトルエン等が挙げられるが、版面に特に優れ
た親油性を付与するためには、ポリスチレン、スチレン
/アクリル酸エステル共重合体、ポリアクリル酸エステ
ル、アクリル酸エステル/アクリル酸エステル共重合体
、及び低融点ポリアミド樹脂を用いることが好ましい。In addition, the binder preferably has a softening point or melting point of 150°C or less by the ring and ball method, and specific examples of such binders include polystyrene, styrene-acrylic ester copolymer, and polyester. -Styrenic resins such as t-butylstyrene, low melting point polyamide resins, polyacrylic esters, acrylic ester/acrylic ester copolymers, polyester resins, ethylene-vinyl acetate copolymers, vinyl chloride-vinyl acetate copolymers, Polymer, vinylidene chloride resin, butyral resin, acetal resin,
Examples include polyvinyltoluene, but in order to impart particularly excellent lipophilicity to the plate surface, polystyrene, styrene/acrylic ester copolymer, polyacrylic ester, acrylic ester/acrylic ester copolymer, and It is preferable to use a low melting point polyamide resin.
本発明においては、前記結着剤は単独もしくは2種以上
併用して用いることもできる。In the present invention, the binders may be used alone or in combination of two or more.
また、熱溶融性物質としては50〜200℃で溶融する
のが好ましく、例えば、カルナバワックス、オーリキュ
リーワックス、マイクロクリスタリンワックス、パラフ
ィンワックス、セレシンワックス、モンタンワックス、
キャンデリラワックス、セラックろう、チュウハクろう
、密ろう1本ろう、低分量ポリエチレン、ステアリン酸
等の脂肪酸、ポリエチレングリコールステアレート等の
ワックス類が挙げられる。Further, the heat-melting substance is preferably melted at 50 to 200°C, and examples thereof include carnauba wax, auriculie wax, microcrystalline wax, paraffin wax, ceresin wax, montan wax,
Examples include waxes such as candelilla wax, shellac wax, wax wax, single beeswax, low-volume polyethylene, fatty acids such as stearic acid, and polyethylene glycol stearate.
本発明で用いる前記無機顔料と結着剤の使用割合は、重
量比で271〜10/1、好ましくは3/1〜7/1が
適当である。The appropriate weight ratio of the inorganic pigment and binder used in the present invention is 271 to 10/1, preferably 3/1 to 7/1.
この使用割合が271未満であると親水性が不足し印刷
物の地肌部が汚れ易く、また10/1を超えると熱印字
した場合の版面の親油性が充分でなく、画像濃度の低下
や画像ムラを生じるので好ましくない。If the usage ratio is less than 271, the hydrophilicity will be insufficient and the background of the printed matter will be easily smudged, and if it exceeds 10/1, the lipophilicity of the printing plate will not be sufficient when thermal printing is performed, resulting in a decrease in image density and image unevenness. This is not desirable because it causes
また、本発明で用いる熱溶融性物質の添加量は、全固形
分に対し0.5〜5重量%、好ましくは1〜3重量%で
ある。0.5重量%未満であると、印刷濃度が不足し、
また5重−M%を超えると印刷物の地汚れが発生するの
で好ましくない。Further, the amount of the heat-fusible substance used in the present invention is 0.5 to 5% by weight, preferably 1 to 3% by weight based on the total solid content. If it is less than 0.5% by weight, the printing density will be insufficient,
Moreover, if it exceeds 5% by weight, it is not preferable because it causes background stains on printed matter.
本発明で用いる支持体としては、例えば、紙、メラミン
−ホルムアルデヒド樹脂、尿素−ホルムアルデヒド樹脂
等で湿潤強化された紙、ポリエチレンテレフタレートの
ような合成樹脂フィルム及びアルミニウム等で蒸着され
た金属蒸着紙等が挙げられる。Examples of the support used in the present invention include paper, paper moist-strengthened with melamine-formaldehyde resin, urea-formaldehyde resin, etc., synthetic resin film such as polyethylene terephthalate, and metal-deposited paper coated with aluminum or the like. Can be mentioned.
また、本発明において、前記必須成分に加え、必要に応
じ塗工液の分散助剤を添加することも可能である。この
ような分散助剤としては、例えばナフテン酸金属塩、脂
肪酸及びその金属塩、カチオン界面活性剤、ノニオン界
面活性剤、アニオン界面活性剤等を挙げることができ、
その添加量は塗工液の固形分に対し通常10重量X以下
とするのがよい。Furthermore, in the present invention, in addition to the above-mentioned essential components, it is also possible to add a dispersion aid for the coating liquid, if necessary. Examples of such dispersion aids include naphthenic acid metal salts, fatty acids and their metal salts, cationic surfactants, nonionic surfactants, anionic surfactants, etc.
The amount added is usually 10% by weight or less based on the solid content of the coating liquid.
本発明の平版印刷用原版は、以下に示すような方法で製
造することができるが、これらの方法に限定されるもの
ではない。The lithographic printing original plate of the present invention can be produced by the following methods, but is not limited to these methods.
まず、前記したプラスチックフィラー、結着剤及び熱溶
融性物質を支持体に塗布し、その塗布面を加熱して中間
層を設ける。First, the above-described plastic filler, binder, and heat-fusible substance are applied to a support, and the coated surface is heated to form an intermediate layer.
次に、無機顔料、結着剤及び熱溶融性物質更に必要に応
じ前記した分散助剤を含む混合物を、ボールミル、アト
ライター、ホモミキサー、グレンミルあるいはサンドミ
ル等の分散機により分t&if1合して感熱記録層塗工
液を作成し、ついでこのものを中間層上にワイヤーバー
、ロールコータ等の従来公知の方法で塗布した後、乾燥
し、必要に応じキャレンダー処理すればよい。中間層に
対する前記感熱記録層塗工液の塗布量は特別の制約はな
いが、−膜内には5g/ rn’〜25g/ mの範囲
とするのがよい。Next, a mixture containing an inorganic pigment, a binder, a heat-melting substance, and, if necessary, the above-mentioned dispersion aid is mixed with a heat-sensitive A recording layer coating solution may be prepared, and then coated onto the intermediate layer by a conventionally known method such as a wire bar or roll coater, dried, and calendered if necessary. There are no particular restrictions on the amount of the heat-sensitive recording layer coating liquid applied to the intermediate layer, but it is preferably within the range of 5 g/rn' to 25 g/m.
本発明で得られた平版印刷用原版を、感熱プリンターあ
るいは感熱ファクシミリ等の熱印字装置により熱印字す
ると、熱印字した部分は熱溶融性物質及び結着剤が溶融
するため、版面で優れた親油性を帯びることとなり、イ
ンキ受容性となる。When the lithographic printing original plate obtained according to the present invention is thermally printed using a thermal printing device such as a thermal printer or a thermal facsimile, the thermally printed area melts the heat-melting substance and the binder, so that the printing plate has excellent adhesive properties. It becomes oily and becomes ink receptive.
一方、非印字部(非画像部)は親水性無機顔料に被覆さ
れており、画像形成後不感脂化処理することにより印刷
可能なものとなる。On the other hand, the non-printing area (non-image area) is coated with a hydrophilic inorganic pigment, and becomes printable by being desensitized after image formation.
本発明の感熱記録型平版印刷用原版は前記構成からなり
、支持体と感熱記録層との間に中間層として中空状プラ
スチックフィラー、熱溶融物質及び結着剤から成る中間
層を有することから、熱感度が向上すると共に、印字部
の親油化度も高まるため印刷品質を大巾に改良すること
ができる。The heat-sensitive recording type lithographic printing original plate of the present invention has the above-mentioned structure, and has an intermediate layer between the support and the heat-sensitive recording layer, which is composed of a hollow plastic filler, a heat-melting substance, and a binder. In addition to improving thermal sensitivity, the degree of lipophilicity of the printed area also increases, so printing quality can be greatly improved.
以下、実施例により本発明を更に詳細に説明する。以下
に示す部はいずれも重量基僧である。Hereinafter, the present invention will be explained in more detail with reference to Examples. All of the sections listed below are based on weight.
実施例1
紙上に発泡性プラスチックフィラー(マイクロスフェア
F−30、松本油脂社jJIJ)30部とポリビニルア
ルコール(クラレボバール117)2部及びS[3R(
ポリラック−750、濃度48%、三井東圧化学社製)
10部、パラフィンワックスエマルジョン(セロゾール
428、濃度50%、中爪油脂社製)1部から成る中間
層塗工液を付着量3〜5 g / raとなるように塗
工して120°Cで2分間乾燥して中間層を形成した。Example 1 30 parts of foamable plastic filler (Microsphere F-30, Matsumoto Yushisha jJIJ), 2 parts of polyvinyl alcohol (Kuraray Bobal 117) and S[3R(
Polylac-750, concentration 48%, manufactured by Mitsui Toatsu Chemical Co., Ltd.)
1 part of paraffin wax emulsion (Cellosol 428, concentration 50%, manufactured by Nakatsume Yushi Co., Ltd.) to a coating weight of 3 to 5 g/ra, and heated at 120°C. It was dried for 2 minutes to form an intermediate layer.
ついで、この中間層上に下記組成からなる感熱記録層塗
工液を乾燥後の付着量がLog/mとなるようにワイヤ
ーバーで塗工し、100℃で1分間乾燥し、ついでスー
パーカレンダー処理して本発明の平版印刷用原版を得た
。Next, a heat-sensitive recording layer coating solution having the following composition was applied onto this intermediate layer using a wire bar so that the coating amount after drying was Log/m, dried at 100°C for 1 minute, and then supercalendered. A lithographic printing original plate of the present invention was obtained.
アクリル樹脂(LR−1551,三菱レーヨン社製、4
0幻と酸化亜鉛(堺化学社製すゼックス#2000)重
量比1:4としてステアリン酸を全固形分の2.5り添
加し1〜ルエンで希釈し40%液としたもの。Acrylic resin (LR-1551, manufactured by Mitsubishi Rayon Co., Ltd., 4
Zinc oxide and zinc oxide (ZEX #2000 manufactured by Sakai Chemical Co., Ltd.) were added with 2.5% of the total solid content of stearic acid at a weight ratio of 1:4, and diluted with 1 to 1 to 1 toluene to make a 40% liquid.
実施例1で得られた感熱記録型平版印刷用原版を、感熱
プリンターあるいは感熱ファクシミリ等の熱印字装置に
より熱印字すると、熱印字した部分は熱溶融性物質及び
結着剤が溶融するため、版面で優れた親油性を帯びるこ
ととなり、インキ受容性となる。一方、非印字部(非画
像部)は親水性無機顔料に被覆されており、画像形成後
不感脂化処理することにより印刷可能なものとなる。When the thermal recording type lithographic printing original plate obtained in Example 1 is subjected to thermal printing using a thermal printing device such as a thermal printer or a thermal facsimile, the thermally printed portion melts the heat-melting substance and the binder, so that the plate surface This results in excellent lipophilicity and ink receptivity. On the other hand, the non-printing area (non-image area) is coated with a hydrophilic inorganic pigment, and becomes printable by being desensitized after image formation.
つぎに、この平版印刷刷版を通常のエツチング処理によ
りエツチングした後、■リコー製オートプリンター印刷
機AP1600にかけ印刷を行ったところ、印刷初期よ
りインク着肉性が良く地汚れのない鮮明かつシャープな
画像を有する印刷物が1000枚以上得られた。Next, after etching this lithographic printing plate using a normal etching process, printing was performed using a Ricoh auto printer AP1600. More than 1000 prints with images were obtained.
実施例2
実施例1において、中間層形成成分のSBRをアクリル
樹脂(AM−200、濃度40%、昭和高分子社製)に
代えた以外は実施例1と同様にして本発明の平版印刷用
原版を得た。Example 2 A lithographic printing material of the present invention was prepared in the same manner as in Example 1 except that SBR as the intermediate layer forming component was replaced with an acrylic resin (AM-200, concentration 40%, manufactured by Showa Kobunshi Co., Ltd.). I got the original version.
実施例3
実施例1において、中間層形成成分のポリビニルアルコ
ールをポリビニルアルコール/グリオキザール(ダイセ
ルGY−60)=7/3に代え、SBRの使用量を4部
とした以外は実施例1と同様にして本発明の平版印刷用
原版を得た。Example 3 The procedure was the same as in Example 1, except that the polyvinyl alcohol as the intermediate layer forming component was replaced with polyvinyl alcohol/glyoxal (Daicel GY-60) = 7/3, and the amount of SBR used was 4 parts. A lithographic printing original plate of the present invention was obtained.
実施例4
実施例1において、中間層形成成分の熱溶融物質である
セロゾール428をポリエチレンワックスエマルジョン
(セロゾール774、濃度34%、中爪油脂社製)に代
えた以外は実施例1と同様にして本発明の平版印刷用原
版を得た。Example 4 The same procedure as in Example 1 was carried out except that in Example 1, Cellosol 428, which is a heat-melting substance as an intermediate layer forming component, was replaced with a polyethylene wax emulsion (Cellosol 774, concentration 34%, manufactured by Nakatsume Yushi Co., Ltd.). A lithographic printing original plate of the present invention was obtained.
つぎに、実施例2〜4で得られた感熱記録型平版印刷用
原版を、感熱プリンターあるいは感熱ファクシミリ等の
熱印字装置により熱印字すると、熱印字した部分は熱溶
融性物質及び結着剤が溶融するため、版面で優れた親油
性を帯びることとなり、インキ受容性となる。一方、非
印字部(非画像部)は親水性無機顔料に被覆されており
、画像形成後不感脂化処理することにより印刷可能なも
のとなる。Next, when the heat-sensitive recording type lithographic printing original plates obtained in Examples 2 to 4 are thermally printed using a thermal printing device such as a thermal printer or a thermal facsimile, the thermally printed areas are free of heat-fusible substances and binders. Because it melts, it has excellent lipophilic properties on the plate surface, making it receptive to ink. On the other hand, the non-printing area (non-image area) is coated with a hydrophilic inorganic pigment, and becomes printable by being desensitized after image formation.
ついで、■リコー製オートプリンター印刷機AP−37
00でエツチング印刷を行なったところ印刷初期よりイ
ンキ着肉性が良く地汚れのない鮮明は印刷物がtooo
枚以上得られた。Next, ■Ricoh auto printer AP-37
When I performed etching printing with 00, the ink receptivity was good from the beginning of printing, and the printed matter was too clear with no background smearing.
I got more than one.
比較例
実施例1において、中間層形成成分の熱溶融物質である
セロゾール−428を削除して比較用の平版印刷用原版
を得た。Comparative Example In Example 1, Cellosol-428, which is a heat-melting substance as an intermediate layer forming component, was omitted to obtain a comparative lithographic printing original plate.
このものを実施例1と同様にサーマルヘッドで印字した
ところスティック音が多発した。印字後年感脂化処理(
エツチング処理)してオフセット印刷したところ画像部
の着肉性が暑くインキ乗りが悪く画像にカスレが生じた
。When this product was printed using a thermal head in the same manner as in Example 1, a lot of sticking noises were produced. Oil sensitization treatment after printing (
When offset printing was performed after etching, the ink adhesion in the image area was hot and ink transfer was poor, resulting in blurring of the image.
特許出願人 株式会社 リ コPatent applicant Rico Co., Ltd.
Claims (1)
主成分とする感熱記録層を設けた感熱記録型平版印刷用
原版において、支持体と感熱記録層との間に中空状プラ
スチックフィラー、熱溶融物質及び結着剤とから成る中
間層を設けたことを特徴とする感熱記録型平版印刷用原
版。(1) In a heat-sensitive recording type lithographic printing original plate in which a heat-sensitive recording layer mainly composed of an inorganic pigment, a binder, and a heat-melting substance is provided on a support, there is a hollow space between the support and the heat-sensitive recording layer. A heat-sensitive recording type lithographic printing original plate characterized by having an intermediate layer comprising a plastic filler, a heat-melting substance, and a binder.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63142647A JPH021389A (en) | 1988-06-09 | 1988-06-09 | Thermal recording type planographic original plate material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63142647A JPH021389A (en) | 1988-06-09 | 1988-06-09 | Thermal recording type planographic original plate material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH021389A true JPH021389A (en) | 1990-01-05 |
Family
ID=15320218
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63142647A Pending JPH021389A (en) | 1988-06-09 | 1988-06-09 | Thermal recording type planographic original plate material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH021389A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04248097A (en) * | 1991-01-25 | 1992-09-03 | Kubota Corp | Pipe body external surface coating device |
-
1988
- 1988-06-09 JP JP63142647A patent/JPH021389A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04248097A (en) * | 1991-01-25 | 1992-09-03 | Kubota Corp | Pipe body external surface coating device |
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