JPS6147404B2 - - Google Patents
Info
- Publication number
- JPS6147404B2 JPS6147404B2 JP15850880A JP15850880A JPS6147404B2 JP S6147404 B2 JPS6147404 B2 JP S6147404B2 JP 15850880 A JP15850880 A JP 15850880A JP 15850880 A JP15850880 A JP 15850880A JP S6147404 B2 JPS6147404 B2 JP S6147404B2
- Authority
- JP
- Japan
- Prior art keywords
- heat
- photosensitive material
- developable photosensitive
- reducing agent
- image
- 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
Links
- 239000000463 material Substances 0.000 claims description 63
- 239000003638 chemical reducing agent Substances 0.000 claims description 42
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 claims description 32
- 229910052709 silver Inorganic materials 0.000 claims description 21
- 239000004332 silver Substances 0.000 claims description 21
- 150000001875 compounds Chemical class 0.000 claims description 19
- -1 silver halide Chemical class 0.000 claims description 12
- 239000011230 binding agent Substances 0.000 claims description 8
- 150000002366 halogen compounds Chemical class 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 239000011247 coating layer Substances 0.000 claims description 2
- 239000002356 single layer Substances 0.000 claims description 2
- 238000007639 printing Methods 0.000 description 52
- 239000010410 layer Substances 0.000 description 23
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 16
- 239000000123 paper Substances 0.000 description 16
- 238000000034 method Methods 0.000 description 11
- 238000011161 development Methods 0.000 description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 150000002894 organic compounds Chemical class 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical group CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 229920002301 cellulose acetate Polymers 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 229910052736 halogen Inorganic materials 0.000 description 5
- 150000002367 halogens Chemical class 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 150000007524 organic acids Chemical class 0.000 description 5
- 238000012546 transfer Methods 0.000 description 5
- 238000002156 mixing Methods 0.000 description 4
- 150000003378 silver Chemical class 0.000 description 4
- AQRYNYUOKMNDDV-UHFFFAOYSA-M silver behenate Chemical compound [Ag+].CCCCCCCCCCCCCCCCCCCCCC([O-])=O AQRYNYUOKMNDDV-UHFFFAOYSA-M 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000000057 synthetic resin Substances 0.000 description 4
- 229920003002 synthetic resin Polymers 0.000 description 4
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 3
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 230000006866 deterioration Effects 0.000 description 3
- 239000004815 dispersion polymer Substances 0.000 description 3
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical group [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- NVXLIZQNSVLKPO-UHFFFAOYSA-N Glucosereductone Chemical compound O=CC(O)C=O NVXLIZQNSVLKPO-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 150000000996 L-ascorbic acids Chemical class 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical group [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical group [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical group [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 235000010323 ascorbic acid Nutrition 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- DIKBFYAXUHHXCS-UHFFFAOYSA-N bromoform Chemical compound BrC(Br)Br DIKBFYAXUHHXCS-UHFFFAOYSA-N 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000010949 copper Chemical group 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- OKJPEAGHQZHRQV-UHFFFAOYSA-N iodoform Chemical compound IC(I)I OKJPEAGHQZHRQV-UHFFFAOYSA-N 0.000 description 2
- 239000011254 layer-forming composition Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 150000004668 long chain fatty acids Chemical class 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 150000004986 phenylenediamines Chemical class 0.000 description 2
- IJAPPYDYQCXOEF-UHFFFAOYSA-N phthalazin-1(2H)-one Chemical compound C1=CC=C2C(=O)NN=CC2=C1 IJAPPYDYQCXOEF-UHFFFAOYSA-N 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical group [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- NDGRWYRVNANFNB-UHFFFAOYSA-N pyrazolidin-3-one Chemical class O=C1CCNN1 NDGRWYRVNANFNB-UHFFFAOYSA-N 0.000 description 2
- 230000001235 sensitizing effect Effects 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- CNHDIAIOKMXOLK-UHFFFAOYSA-N toluquinol Chemical compound CC1=CC(O)=CC=C1O CNHDIAIOKMXOLK-UHFFFAOYSA-N 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Chemical group 0.000 description 2
- ZPANWZBSGMDWON-UHFFFAOYSA-N 1-[(2-hydroxynaphthalen-1-yl)methyl]naphthalen-2-ol Chemical compound C1=CC=C2C(CC3=C4C=CC=CC4=CC=C3O)=C(O)C=CC2=C1 ZPANWZBSGMDWON-UHFFFAOYSA-N 0.000 description 1
- NSCYCXXUGOPSRI-UHFFFAOYSA-N 2,3,5-trihydroxyphthalazine-1,4-dione Chemical compound O=C1N(O)N(O)C(=O)C2=C1C(O)=CC=C2 NSCYCXXUGOPSRI-UHFFFAOYSA-N 0.000 description 1
- REFDOIWRJDGBHY-UHFFFAOYSA-N 2-bromobenzene-1,4-diol Chemical compound OC1=CC=C(O)C(Br)=C1 REFDOIWRJDGBHY-UHFFFAOYSA-N 0.000 description 1
- DFZVZKUDBIJAHK-UHFFFAOYSA-N 2-hydroxyoctadecanoic acid silver Chemical compound [Ag].OC(C(=O)O)CCCCCCCCCCCCCCCC DFZVZKUDBIJAHK-UHFFFAOYSA-N 0.000 description 1
- SRJCJJKWVSSELL-UHFFFAOYSA-N 2-methylnaphthalen-1-ol Chemical compound C1=CC=CC2=C(O)C(C)=CC=C21 SRJCJJKWVSSELL-UHFFFAOYSA-N 0.000 description 1
- PFANXOISJYKQRP-UHFFFAOYSA-N 2-tert-butyl-4-[1-(5-tert-butyl-4-hydroxy-2-methylphenyl)butyl]-5-methylphenol Chemical compound C=1C(C(C)(C)C)=C(O)C=C(C)C=1C(CCC)C1=CC(C(C)(C)C)=C(O)C=C1C PFANXOISJYKQRP-UHFFFAOYSA-N 0.000 description 1
- LZHCVNIARUXHAL-UHFFFAOYSA-N 2-tert-butyl-4-ethylphenol Chemical compound CCC1=CC=C(O)C(C(C)(C)C)=C1 LZHCVNIARUXHAL-UHFFFAOYSA-N 0.000 description 1
- XOUQAVYLRNOXDO-UHFFFAOYSA-N 2-tert-butyl-5-methylphenol Chemical compound CC1=CC=C(C(C)(C)C)C(O)=C1 XOUQAVYLRNOXDO-UHFFFAOYSA-N 0.000 description 1
- ZVNPWFOVUDMGRP-UHFFFAOYSA-N 4-methylaminophenol sulfate Chemical compound OS(O)(=O)=O.CNC1=CC=C(O)C=C1.CNC1=CC=C(O)C=C1 ZVNPWFOVUDMGRP-UHFFFAOYSA-N 0.000 description 1
- OORIFUHRGQKYEV-UHFFFAOYSA-N 6-bromo-1-(6-bromo-2-hydroxynaphthalen-1-yl)naphthalen-2-ol Chemical group BrC1=CC=C2C(C3=C4C=CC(Br)=CC4=CC=C3O)=C(O)C=CC2=C1 OORIFUHRGQKYEV-UHFFFAOYSA-N 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- VZBILKJHDPEENF-UHFFFAOYSA-M C3-thiacarbocyanine Chemical compound [I-].S1C2=CC=CC=C2[N+](CC)=C1C=CC=C1N(CC)C2=CC=CC=C2S1 VZBILKJHDPEENF-UHFFFAOYSA-M 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical group [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 229920008347 Cellulose acetate propionate Polymers 0.000 description 1
- 229920001747 Cellulose diacetate Polymers 0.000 description 1
- DQEFEBPAPFSJLV-UHFFFAOYSA-N Cellulose propionate Chemical compound CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 DQEFEBPAPFSJLV-UHFFFAOYSA-N 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical group [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical group [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical group [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical group [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
- SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 1
- HOLVRJRSWZOAJU-UHFFFAOYSA-N [Ag].ICl Chemical compound [Ag].ICl HOLVRJRSWZOAJU-UHFFFAOYSA-N 0.000 description 1
- NZHXEWZGTQSYJM-UHFFFAOYSA-N [bromo(diphenyl)methyl]benzene Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(Br)C1=CC=CC=C1 NZHXEWZGTQSYJM-UHFFFAOYSA-N 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- WRYNUJYAXVDTCB-UHFFFAOYSA-M acetyloxymercury Chemical compound CC(=O)O[Hg] WRYNUJYAXVDTCB-UHFFFAOYSA-M 0.000 description 1
- 238000000498 ball milling Methods 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical group [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 229910052790 beryllium Inorganic materials 0.000 description 1
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical group [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical group [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 229950005228 bromoform Drugs 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical group [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 229910052792 caesium Inorganic materials 0.000 description 1
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical group [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Chemical group 0.000 description 1
- 229910001622 calcium bromide Inorganic materials 0.000 description 1
- WGEFECGEFUFIQW-UHFFFAOYSA-L calcium dibromide Chemical compound [Ca+2].[Br-].[Br-] WGEFECGEFUFIQW-UHFFFAOYSA-L 0.000 description 1
- VZGDMQKNWNREIO-UHFFFAOYSA-N carbon tetrachloride Substances ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- UOCJDOLVGGIYIQ-PBFPGSCMSA-N cefatrizine Chemical group S([C@@H]1[C@@H](C(N1C=1C(O)=O)=O)NC(=O)[C@H](N)C=2C=CC(O)=CC=2)CC=1CSC=1C=NNN=1 UOCJDOLVGGIYIQ-PBFPGSCMSA-N 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 229920006218 cellulose propionate Polymers 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- AJPXTSMULZANCB-UHFFFAOYSA-N chlorohydroquinone Chemical compound OC1=CC=C(O)C(Cl)=C1 AJPXTSMULZANCB-UHFFFAOYSA-N 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Chemical group 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Chemical group 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical group [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 229920001940 conductive polymer Polymers 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- VUFOSBDICLTFMS-UHFFFAOYSA-M ethyl-hexadecyl-dimethylazanium;bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)CC VUFOSBDICLTFMS-UHFFFAOYSA-M 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 229910052733 gallium Inorganic materials 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
- 150000004820 halides Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002431 hydrogen Chemical group 0.000 description 1
- NWVVVBRKAWDGAB-UHFFFAOYSA-N hydroquinone methyl ether Natural products COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 125000001841 imino group Chemical group [H]N=* 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical group [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910052746 lanthanum Inorganic materials 0.000 description 1
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical group [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 description 1
- 239000011133 lead Chemical group 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Chemical group 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical group [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
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- VBTQNRFWXBXZQR-UHFFFAOYSA-N n-bromoacetamide Chemical compound CC(=O)NBr VBTQNRFWXBXZQR-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- CMCWWLVWPDLCRM-UHFFFAOYSA-N phenidone Chemical compound N1C(=O)CCN1C1=CC=CC=C1 CMCWWLVWPDLCRM-UHFFFAOYSA-N 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002432 poly(vinyl methyl ether) polymer Polymers 0.000 description 1
- 229920006289 polycarbonate film Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Chemical group 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical group [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical group [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 1
- YRSQDSCQMOUOKO-KVVVOXFISA-M silver;(z)-octadec-9-enoate Chemical compound [Ag+].CCCCCCCC\C=C/CCCCCCCC([O-])=O YRSQDSCQMOUOKO-KVVVOXFISA-M 0.000 description 1
- OIZSSBDNMBMYFL-UHFFFAOYSA-M silver;decanoate Chemical compound [Ag+].CCCCCCCCCC([O-])=O OIZSSBDNMBMYFL-UHFFFAOYSA-M 0.000 description 1
- MNMYRUHURLPFQW-UHFFFAOYSA-M silver;dodecanoate Chemical compound [Ag+].CCCCCCCCCCCC([O-])=O MNMYRUHURLPFQW-UHFFFAOYSA-M 0.000 description 1
- LTYHQUJGIQUHMS-UHFFFAOYSA-M silver;hexadecanoate Chemical compound [Ag+].CCCCCCCCCCCCCCCC([O-])=O LTYHQUJGIQUHMS-UHFFFAOYSA-M 0.000 description 1
- ORYURPRSXLUCSS-UHFFFAOYSA-M silver;octadecanoate Chemical compound [Ag+].CCCCCCCCCCCCCCCCCC([O-])=O ORYURPRSXLUCSS-UHFFFAOYSA-M 0.000 description 1
- OHGHHPYRRURLHR-UHFFFAOYSA-M silver;tetradecanoate Chemical compound [Ag+].CCCCCCCCCCCCCC([O-])=O OHGHHPYRRURLHR-UHFFFAOYSA-M 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical group [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000002123 temporal effect Effects 0.000 description 1
- 229910052716 thallium Inorganic materials 0.000 description 1
- BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical group [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
- JBWKIWSBJXDJDT-UHFFFAOYSA-N triphenylmethyl chloride Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(Cl)C1=CC=CC=C1 JBWKIWSBJXDJDT-UHFFFAOYSA-N 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
- 238000007740 vapor deposition Methods 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/494—Silver salt compositions other than silver halide emulsions; Photothermographic systems ; Thermographic systems using noble metal compounds
- G03C1/498—Photothermographic systems, e.g. dry silver
- G03C1/49827—Reducing agents
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Photoreceptors In Electrophotography (AREA)
- Printing Methods (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Description
本発明は、熱現像性感光材料に関し、詳しくは
静電印刷マスターに適した有機銀塩を含有する改
良された熱現像性感光材料に関するものである。
従来から印刷方法として、非常に数多くの方法
が知られているが、その中で静電印刷法は、特異
な印刷分野を成している。通常の印刷技術は、印
刷マスター表面に形成されている凹凸面、或い
は、溶剤親和性の差に従つて、インキを印刷マス
ター面に選択的に附着させて、これに紙を圧着さ
せることに基いている。これに対し、静電印刷法
では、機械的(または物理的)にインキを印刷マ
スターに附着させるのとは異なり、静電的にイン
キ(トナー)を付着させて、これを紙に転用する
ことに基いている。この静電印刷法は、例えば特
開昭51―24308号公報などに記載されている。
上述の静電印刷法に用いる静電印刷マスターは
静電荷を保持するに充分な電気抵抗を有する絶縁
性媒体中に担持された銀像を主体として成る層を
有するものである事から画像が凹凸によつて形成
されてなく表面が平滑であるので、従つて印刷時
等に於ける機械的摩擦によつて画像が損傷を受け
る事が殆んどなく、耐久性に優れている事、銀像
自体の高解像性、連続階調性等に因る解像力の優
秀性、光学濃度を任意の連続階調に従つて変える
事が出来る等の優れた点を数多有し、印刷分野の
みならず多数枚高速複写の分野に於いて多大なる
期待が寄せられ、その実用化の早急が望まれてい
るところである。通常、前述の銀像を主体として
成る層を有する静電印刷マスターは銀塩感光材料
に画像露光し現像する事で得られるものであり、
その中で所謂銀液を乾式処理で形成出来る事から
有機銀塩、有機銀塩に対して触媒量のハロゲン化
銀、絶縁性媒体及び必要に応じて還元剤を含む感
光材料の採用は、その画像作成の簡易性の点から
有効なものである。
この様な感光材料は、所謂熱現像性感光材料と
称されているもので、従来のものとしては、例え
ば特公昭43―4924号公報、特公昭46―7782号公
報、特公昭47―11113号公報などに記載されてい
るし、また従来から市販されているものである。
しかしながら、これら従来の熱現像性感光材料
は、何れも最終的な可視画像を直接熱現像性感光
材料に形成するもので、所謂複写用の熱現像性感
光材料であり、本出願人が先に提案した特開昭51
―24308号に記載されている静電印刷マスター形
成用として実用性の点からそのままでは全く使用
出来ないものである。従つて本出願人は先の特開
昭51―24308号に於いて静電印刷マスター用熱現
像性感光材料として、静電印刷マスターとしての
特性を有し、実用性、商業性に富む様改良改善を
図つたものである。
本発明は、斯かる熱現像性感光材料を静電印刷
マスター形成用の感光材料として改めて多方面か
ら充分検討した結果、更に改良改善をす可き点の
ある事を見出し、その点を鑑みて鋭意研究する事
により技術的にも商業的にも静電印刷マスターと
しての緒条件を充分満足する静電印刷マスターの
得られる熱現像性感光材料の開発に成功したもの
である。
即ち、静電印刷マスターとしては、非銀像部に
於ける受容電位が高い事、静電荷保持性が良い
事、静電コントラストが高い事、銀像部における
残留電位が低い事、最終的に得られる例えばトナ
ー画像性(シヤープネス)及び耐刷性、耐電気的
疲労性に優れている事、機械的強度が充分ある事
等の緒性能条件が要求され、更にこれ等の条件に
加えて静電印刷マスターの形成が簡便且つ容易
に、短時間で成され得る事、熱現像性感光材料の
製造そのものが簡易に成され得る事、低コストで
あり輸送運搬に特別の処置が必要無く、流通性に
優れている事等の条件が要求されるものであつ
て、本発明は上述の緒条件を満足する極めて商業
的価値の高い優れた特性を有する静電印刷マスタ
ー用熱現像性感光材料を提供する事を主たる目的
とするものである。
また、本発明の別の目的は、新規な熱現像性感
光材料を提供することにある。
本発明の熱現像性感光材料、特に静電印刷法に
適した熱現像性感光材料は、(c)還元剤として下記
一般式〔〕で示される化合物の少なくとも1種
を含有することに特徴を有し、これにより静電特
性が顕著に改善され、その静電印刷用マスターと
しての性能が飛躍的に向上する。
一般式〔〕
式中、R1およびR2は、第3級アルキル基(例
えば、t―ブチル基、t―アミル基、t―オクチ
ル基など)を示し、R3およびR4は置換若しくは
非置換のアルキル基(例えば、メチル基、エチル
基、n―プロピル基、iso―プロピル基、n―ブ
チル基、t―ブチル基、ベンジル基、P―クロロ
ベンジル基など)を示す。nは、1〜4の整数で
ある。
前記一般式〔〕で示される化合物の具体例
は、下記のとおりである。
化合物例
本発明の熱現像性感光材料は、支持体上に、少
なくとも(a)有機銀塩、(b)感光性ハロゲン化銀若し
くは前記(a)有機銀塩と反応させてハロゲン化銀を
形成しうるハロゲン化合物、前述の(c)還元剤およ
び(d)結着剤からなる被覆層を単層若しくは積層構
造で設けた構成を有している。この熱現像性感光
材料は、例えば有機銀塩とハロゲン化合物を絶縁
性媒体である結着剤中に混合分散させて、適当な
支持体上に塗布して有機銀塩層を形成し、次いで
前述の還元剤を適当な溶剤を用いて酢酸セルロー
スなどの樹脂からなる結着剤と混合して、先に形
成させた有機銀塩層の表面に塗布して還元剤層を
設けることによつて調製される。また、前述の還
元剤を有機銀塩とともに用いてもよく、この際、
別に還元剤層を設けていても差支えない。その他
に、前述の還元剤を、画像露光の前または後で有
機銀塩層に塗布することによつて含有させてもよ
い。
本発明において好ましく使用される(a)有機銀塩
としては、特公昭43―4924号公報、特開昭52―
90306号公報などに記載されている有機酸、メル
カプト化合物、イミノ化合物などの銀塩および有
機銀錯塩などが挙げられるが、特に室内光下で暗
着色化などの不都合な変化を受け難いものとし
て、例えばベヘン酸銀、ステアリン酸銀、パルミ
チン酸銀、ミリスチン酸銀、ラウリン酸銀、オレ
イン酸銀、ヒドロキシステアリン酸銀などの長鎖
脂肪酸の銀塩が好適である。
本発明において好ましく使用される(b)ハロゲン
化合物としては、下記に示す無機ハロゲン化合物
あるいは含ハロゲン有機化合物が具体例として挙
げられる。
(1) 無機ハロゲン化合物
無機ハロゲン化合物としては一般式MXmで表
わされるものが好適なものである。式中Xはハロ
ゲン(Cl,Br,I)を示し、mが2以上の場合
にはXは同種のハロゲンでも異なるハロゲンでも
良い。Mは水素、カルシウム、ストロンチウム、
カドミウム、クロム、ルビジウム、銅、ニツケ
ル、マグネシウム、亜鉛、鉛、白金、パラジウ
ム、ビスマス、タリウム、ルテニウム、ガリウ
ム、インジウム、ロジウム、ベリリウム、コバル
ト、水銀、バリウム、銀、セシウム、ランタン、
イリジウム、アルミニウムなどを示し、mは水素
の場合は1であり、Mが金属の場合はその原子価
を示す。更に塩臭化銀、塩臭沃化銀、臭沃化銀、
塩沃化銀も好適に採用される。
(2) 含ハロゲン有機化合物
四塩化炭素、クロロホルム、トリクロルエチレ
ン、塩化トリフエニルメチル、臭化トリフエニル
メチル、ヨードホルム、プロモホルム、セチルエ
チルジメチルアンモニウムブロマイド等である。
前述のハロゲン化物(1)又は(2)は単独若しくは二種
以上併用して使用しても差支えないものであり、
その添加量は通常有機銀塩1molに対して1mol以
下、好適には10-1mol乃至10-5molが望ましいも
のである。
本発明においては、(c)還元剤として前述の一般
式〔〕で表わされる化合物と組合わせて以下に
示す様な他の還元剤を使用することによつて、一
層好ましい結果が得られる。これらの還元剤とし
ては、アミノフエノール類、フエニレンジアミン
類、ポリヒドロキシベンゼン類、アスコルビン酸
類、3―ピラゾリドン類、オキシテトロン酸類、
ヒドロキシテトロンイミド類あるいはレダクトン
系還元剤が含まれる。
これらの代表例としては、ハイドロキノン;メ
チルハイドロキノン;クロロハイドロキノン;ブ
ロモハイドロキノン;カテコール;ピロガロー
ル;メチルヒドロキシナフタレン;アミノフエノ
ール;2,2′―メチレンビス(6―t―ブチル―
4―メチルフエノール);4,4′―ブチリデンビ
ス(6―t―ブチル―3―メチルフエノール);
4,4′―ビス(6―t―ブチル―3―メチルフエ
ノール);4,4′―チオビス(6―t―2―メチ
ルフエノール);2,6―ジ―t―ブチル―p―
クレゾール;2×2′―メチレンビス(4―エチル―
6―t―ブチルフエノール);フエニドン;メト
ール;2,2′―ヒドロキシ―1,1′―ビナフチ
ル;6,6′―ジブロモー2,2′―ジヒドロキシ―
1,1′―ビナフチル;ビス(2―ヒドロキシ―1
―ナフチル)メタン、2,2′―メチレンビス―
(6―t―ブチル―p―クレゾール)及び、これ
らの混合物等が挙げられる。
本発明の熱現像性感光材料に用いる前記一般式
〔〕で示される還元剤の含有量は、所望される
特性に応じて適宜決められるものであるが、一般
的に有機銀塩1モルに対して5モル以下、好適に
は1モル以下、最適には1モル〜10-4モルであ
る。また、他の還元剤と併用して含有させる場合
にも、還元剤の総量として上記同様の添加量で含
有させることができる。この際、前記一般式
〔〕で示される還元剤の割合を還元剤の総量に
対して10重量%以上とすることが好ましい。
更に本発明の静電印刷マスター用熱現像性感光
材料に於いては得られる画像の色調を制御するた
めの調色剤や長期保存する際、特に重要となる画
像の安定性を附与するための安定化剤、画像形成
前に於ける熱現像性感光材料の保存の際の、所謂
光による被り防止及び画像形成後に於ける被りに
依る画像の時間的変化の防止のための耐光剤、更
には増感色素、現像促進剤、等の成分を所望とさ
れる熱現像性感光材料の特性に応じて必要量添加
されても良いものである。
本発明において使用される好ましい結着剤、特
に絶縁性を示すものとしては、ゼラチン、ポリビ
ニルブチラール、ポリ酢酸ビニル、二酢酸セルロ
ース、三酢酸セルロース、セルロースアセテート
ブチレート、ポリビニルアルコール、エチルセル
ロース、メチルセルロース、ベンジルセルロー
ス、ポリビニルアセタール、セルロースプロピオ
ネート、セルロースアセテートプロピオネート、
ヒドロキシエチルセルロース、エチルヒドロキシ
セルロース、カルボキシメチルセルロース、ポリ
ビニルホルマール、ポリビニルメチルエーテル、
スチレン―ブタジエン共重合体、ポリメチルメタ
アクリルレート等が挙げられ、必要に応じてこれ
ら化合物を二種以上混合して使用しても良いもの
である。
これらの結着剤の量は所望に応じて適宜決定さ
れるものであるが有機銀塩1重量部に対して通常
は0.02乃至20重量部であり、好適には0.1乃至5
重量部であるのが望ましいものである。
更に支持体として採用されるのはアルミ、銅、
亜鉛、銀などの金属板或いは金属ラミネート紙、
アート紙、溶剤が内部に浸入しない様に処理した
紙、更に導電性ポリマーを処理した紙、界面活性
剤を混入した合成樹脂フイルム、蒸着法により表
面に金属または金属酸化物または金属ハロゲン化
物を密着させたガラスまたは紙、合成樹脂、酢酸
セルロースフイルム、ポリエチレンテレフタレー
トフイルム、ポリカーボネートフイルム、ポリス
チレンフイルム等のフイルム等を用いることがで
きる。また、絶縁性の、ガラス、紙、合成樹脂等
も用いてもよい。特にドラムに巻きつけて使用す
る場合には適当な柔軟性のある金属シート、紙或
いは他の導電性の材料でドラムに巻きつけられる
様に工夫したものが良い。この様なものとして殊
に、支持体としての特性及び安価であること等の
利点からアート紙は好適である。
合成樹脂フイルム、紙或いはその他の非導電性
支持体の表面に導電層を設ける場合、支持体の有
機銀塩層側でも該層とは反対側の面でも使用目的
に応じて適宜選択されるが導電層が有機銀塩層と
直に接触する様な場合には、その導電層形成材料
は有機銀塩と反応しない様な材料を選択するのが
好ましいものである。
導電性支持体を採用する場合には、一般には表
面固有抵抗値が静電印刷マスターを形成した場合
の非銀像部より小さいもの、即ち、109Ω・cm以
下、好ましくは105Ω・cm以下ものであつて、有
機銀塩と反応しないものであれば何を採用しても
良いものである。
本発明の熱現像性感光材料を用いて静電印刷マ
スターを形成するには、有機銀塩上に還元剤層が
設けられている構成に於ては通常画像露光して潜
像を形成し、次いで熱現像して、銀像を形成して
マスターとするものである。又、予め還元剤が含
有されていない熱現像性感光材料に於ては、画像
露光前又は後に還元剤を附与し、潜像形成及び熱
現像を施こすことで静電印刷マスターが形成され
る。還元剤の附与方法としては使用時に於て画像
露光前の熱現像性感光材料を還元剤の含有されて
いる液体中に浸漬して還元剤を附与しても良い
し、又、画像露光後熱現像前に同様の処理で還元
剤を付与しても良い。又、前述の浸漬法の代わり
に適宜な溶剤を使用して酢酸セルロース等に分散
させた還元剤溶液を刷毛塗、コーテイング、ドク
ターブレード、スプレー等の方法で有機銀塩層上
に塗布しても良い。
尚還元剤層は熱現像後、有機銀塩層表面から剥
離すれば、残存する還元剤の作用による所謂被り
防止になるので好都合である。
以上、本発明の熱現像性感光材料が特に静電特
性に優れているために、その用途として静電印刷
用マスターのみの例を挙げて詳細に述べてきた
が、本発明の熱現像性感光材料の用途としては、
前述の静電印刷マスター形成用の熱現像性感光材
料に用いられることに限定されるものではなく、
通常の画像露光および熱現像を順に操作すること
によつて可視画像を形成させるための熱現像性感
光材料として、あるいはその他の光記録材料とし
ても使用できる。
以下、本発明を実施例に従つて説明する。
実施例 1
90mol%ベヘン酸銀*25g、メチルエチルケト
ン120gおよびトルエン120gをボールミリング法
により72時間以上混合分散した。しかるのち、ポ
リビニルブチラール(20wt%エチルアルコール
溶液)56.5gを加え十分混合し、有機銀塩のポリ
マー分散液を調製した。
こうして調製したポリマー分散液に臭化カルシ
ウム200mg/25mlメチルアルコール溶液、フタラ
ジノン2.5g、酢酸水銀120mg/25mlおよびメチル
アルコール溶液を加えて更に十分混合を行つた。
次に、このポリマー分散液をアート紙上にコーテ
イングロツドにより、乾燥後の膜厚が8μとなる
ように暗所で塗布し、有機銀塩層を形成した。
〔*90mol%ベヘン酸銀とは有機酸の銀塩の
mol数を有機酸のmol数と有機酸の銀塩のmol数と
を加えた値で除し、その値を100倍した割合を有
する有機酸の銀塩において、この有機酸の銀塩が
ベヘン酸銀の場合を意味する。以下の実施例にお
ける有機酸銀塩のmol%は前記の意味を示すもの
とする。〕
次に、前記例示化合物(1)1.5g、フタラジノン
0.3g、酢酸セルロース(10重量%アセトン溶
液)10g、アセトン30gおよび増感色素として下
記化合物9mgを混合し、上塗層溶液とした。
この上塗層溶液を前記有機銀塩層上に乾燥後の
膜厚が4μとなるように暗所で塗布し、静電印刷
マスター形成用熱現像性感光材料(試料1)とし
た。
次に、この感光材料に陽画を介して、タングス
テン光源(2500ルツクス)を用い、20秒間の露光
を行つた後、ローラー式加熱装置を用いて130
℃、5秒間の加熱現像によつて陰画のプリント可
視画像を得、静電印刷用マスターとした。
次いで、+6KVのコロナ放電を前記静電印刷用
マスターに均一に与えた後、負に帯電したトナー
をマグネブラシ現像法により現像したところ、陽
画のトナー画像が得られた。
このトナー画像上に転写紙をかさねて、転写紙
側から前記のコロナ放電を与えると鮮明な転写可
視画像が得られた。
この帯電と現像転写を繰り返して、転写回数が
1000回以上でもマスター表面には何ら劣化が認め
られず、転写画像の画質が悪くなることは認めら
れなかつた。更に長時間使用した後でも得られる
転写画像の悪化は何ら認められなかつた。
この結果、繰り返し印刷用のマスターとして非
常に優れていることが認められた。
また、銀画像は原画に対して忠実な再現性を示
すので、それに応じた静電荷像が形成され、トナ
ー画像もそれに応じて忠実な写真画像になつてい
ることが認められた。
そこで、この静電印刷用マスターの静電特性を
測定したところ、画像部(銀像部)と非画像部
(非銀像部)との帯電電位差(静電コントラス
ト)は700Vを示し、更に残留電位が非常に小さ
いことがわかつた。次に、前記マスターの画像部
の最大黒化反射濃度(Dmax)を測定したところ
1.65を示した。更に転写画像のある転写紙上の非
画像部の黒化反射濃度(カブリ濃度)を測定した
ところ0.20と非常に小さな値であつた。以上の測
定から本実施例における静電印刷マスター形成用
熱現像性感光材料は画像性に優れ、前記かつ耐刷
性の良い実用に耐える優れた静電印刷用マスター
を形成することがわかつた。
実施例 2〜5
前記実施例1で用いた静電印刷マスター用熱現
像性感光材料を作成した時に使用した上塗層溶液
中の還元剤成分として前記例示化合物(1)に代え
て、前記例示化合物(1)―「A」と記す―と2,2
―メチレンビス(6―t―ブチル―P―クレゾー
ル)―「B」と記す―を第1表に示す混合比で併
用したほかは、同様の方法によつて静電印刷マス
ター用熱現像性感光材料を作成した。この熱現像
性感光材料に実施例1と同様の方法によつて像露
光および熱現像を施こして静電印刷マスターを作
成した。次いで、同様の方法によつて静電特性を
測定した。これらの結果を第1表に示す。
The present invention relates to a heat-developable photosensitive material, and more particularly to an improved heat-developable photosensitive material containing an organic silver salt suitable for an electrostatic printing master. A large number of printing methods have been known so far, but electrostatic printing constitutes a unique field of printing. Ordinary printing technology is based on selectively adhering ink to the printing master surface according to the uneven surface formed on the printing master surface or the difference in solvent affinity, and pressing paper onto this. I'm there. On the other hand, in the electrostatic printing method, unlike mechanically (or physically) applying ink to a printing master, ink (toner) is applied electrostatically and this is transferred to paper. It is based on This electrostatic printing method is described in, for example, Japanese Patent Laid-Open No. 51-24308. The electrostatic printing master used in the electrostatic printing method described above has a layer mainly consisting of a silver image supported on an insulating medium that has sufficient electrical resistance to hold electrostatic charges, so the image is uneven. Since the surface is smooth and not formed by silver, the image is hardly damaged by mechanical friction during printing, and has excellent durability. It has many excellent features such as its high resolution, excellent resolution due to continuous gradation, and the ability to change optical density according to any continuous gradation, and is useful only in the printing field. There are great expectations in the field of high-speed, multi-sheet copying, and its practical application is desired as soon as possible. Usually, the electrostatic printing master having a layer mainly composed of the above-mentioned silver image is obtained by imagewise exposure and development of a silver salt photosensitive material.
Among them, the so-called silver liquid can be formed by dry processing, so the adoption of photosensitive materials containing organic silver salts, catalytic amounts of silver halide, an insulating medium, and reducing agents as necessary for the organic silver salts is important. This is effective in terms of the simplicity of image creation. Such photosensitive materials are called heat-developable photosensitive materials, and conventional ones include, for example, Japanese Patent Publication No. 43-4924, Japanese Patent Publication No. 7782-1978, and Japanese Patent Publication No. 47-11113. It is described in publications and has been commercially available. However, all of these conventional heat-developable photosensitive materials are those in which the final visible image is directly formed on the heat-developable photosensitive material, and are so-called heat-developable photosensitive materials for copying. Proposed Japanese Patent Application Publication No. 1973
- From the practical point of view, it cannot be used as it is for forming an electrostatic printing master as described in No. 24308. Therefore, the present applicant has improved the heat-developable photosensitive material for electrostatic printing master in the previous Japanese Patent Application Laid-open No. 51-24308 so that it has the characteristics as an electrostatic printing master and is highly practical and commercially viable. This is an improvement. The present invention is based on the results of thorough examination from various aspects of such a heat-developable photosensitive material as a photosensitive material for forming an electrostatic printing master, and after discovering that there are points that need further improvement. Through intensive research, we have succeeded in developing a heat-developable photosensitive material that can be used as an electrostatic printing master that fully satisfies the requirements for an electrostatic printing master both technically and commercially. In other words, as an electrostatic printing master, it has to have a high acceptance potential in non-silver image areas, good electrostatic charge retention, high electrostatic contrast, and low residual potential in silver image areas. For example, toner performance conditions such as excellent toner image quality (sharpness), printing durability, electrical fatigue resistance, and sufficient mechanical strength are required, and in addition to these conditions, static The electroprinting master can be formed simply and easily in a short time, the production of the heat-developable photosensitive material itself can be done easily, the cost is low, no special treatment is required for transportation, and distribution is easy. The present invention provides a heat-developable photosensitive material for electrostatic printing masters that satisfies the above-mentioned conditions and has excellent properties that have extremely high commercial value. The main purpose is to provide Another object of the present invention is to provide a novel heat-developable photosensitive material. The heat-developable photosensitive material of the present invention, particularly the heat-developable photosensitive material suitable for electrostatic printing, is characterized by containing at least one compound represented by the following general formula [] as (c) a reducing agent. As a result, the electrostatic properties are significantly improved, and the performance as a master for electrostatic printing is dramatically improved. General formula [] In the formula, R 1 and R 2 represent a tertiary alkyl group (e.g., t-butyl group, t-amyl group, t-octyl group, etc.), and R 3 and R 4 represent a substituted or unsubstituted alkyl group. (For example, methyl group, ethyl group, n-propyl group, iso-propyl group, n-butyl group, t-butyl group, benzyl group, P-chlorobenzyl group, etc.). n is an integer from 1 to 4. Specific examples of the compound represented by the general formula [] are as follows. Compound example The heat-developable photosensitive material of the present invention can be reacted with at least (a) an organic silver salt, (b) a photosensitive silver halide, or the above (a) organic silver salt to form a silver halide on a support. It has a structure in which a coating layer consisting of a halogen compound, the above-mentioned (c) reducing agent, and (d) binder is provided in a single layer or a laminated structure. This heat-developable photosensitive material is produced by, for example, mixing and dispersing an organic silver salt and a halogen compound in a binder, which is an insulating medium, and coating the mixture on a suitable support to form an organic silver salt layer. A reducing agent layer is prepared by mixing a reducing agent with a binder made of a resin such as cellulose acetate using an appropriate solvent and applying the mixture to the surface of the organic silver salt layer previously formed to form a reducing agent layer. be done. Further, the above-mentioned reducing agent may be used together with an organic silver salt, and in this case,
There is no problem even if a reducing agent layer is provided separately. Alternatively, the above-mentioned reducing agent may be incorporated by coating the organic silver salt layer before or after image exposure. The organic silver salt (a) preferably used in the present invention is disclosed in Japanese Patent Publication No. 4924/1983,
Examples include silver salts and organic silver complex salts such as organic acids, mercapto compounds, and imino compounds described in Publication No. 90306, etc.; For example, silver salts of long-chain fatty acids such as silver behenate, silver stearate, silver palmitate, silver myristate, silver laurate, silver oleate, and silver hydroxystearate are suitable. Specific examples of the halogen compound (b) preferably used in the present invention include the following inorganic halogen compounds and halogen-containing organic compounds. (1) Inorganic halogen compound The preferred inorganic halogen compound is one represented by the general formula MXm. In the formula, X represents halogen (Cl, Br, I), and when m is 2 or more, X may be the same type of halogen or different halogens. M is hydrogen, calcium, strontium,
Cadmium, chromium, rubidium, copper, nickel, magnesium, zinc, lead, platinum, palladium, bismuth, thallium, ruthenium, gallium, indium, rhodium, beryllium, cobalt, mercury, barium, silver, cesium, lanthanum,
Indicates iridium, aluminum, etc., where m is 1 when hydrogen is present, and when M is a metal, it indicates its valence. Furthermore, silver chlorobromide, silver chlorobromoiodide, silver bromoiodide,
Silver chloroiodide is also suitably employed. (2) Halogen-containing organic compounds Carbon tetrachloride, chloroform, trichloroethylene, triphenylmethyl chloride, triphenylmethyl bromide, iodoform, bromoform, cetylethyldimethylammonium bromide, etc.
The above-mentioned halides (1) or (2) may be used alone or in combination of two or more,
The amount added is usually 1 mol or less, preferably 10 -1 mol to 10 -5 mol, per 1 mol of organic silver salt. In the present invention, more preferable results can be obtained by using other reducing agents as shown below in combination with the compound represented by the above-mentioned general formula [] as the reducing agent (c). These reducing agents include aminophenols, phenylenediamines, polyhydroxybenzenes, ascorbic acids, 3-pyrazolidones, oxytetronic acids,
Contains hydroxytetronimides or reductone reducing agents. Representative examples of these include hydroquinone; methylhydroquinone; chlorohydroquinone; bromohydroquinone; catechol; pyrogallol; methylhydroxynaphthalene; aminophenol; 2,2'-methylenebis(6-t-butyl-
4-methylphenol); 4,4'-butylidenebis(6-t-butyl-3-methylphenol);
4,4'-bis(6-t-butyl-3-methylphenol);4,4'-thiobis(6-t-2-methylphenol); 2,6-di-t-butyl-p-
Cresol; 2 × 2′-methylenebis(4-ethyl-
6-tert-butylphenol); phenidone; metol; 2,2'-hydroxy-1,1'-binaphthyl;6,6'-dibromo2,2'-dihydroxy-
1,1'-binaphthyl; bis(2-hydroxy-1
-naphthyl)methane, 2,2'-methylenebis-
(6-t-butyl-p-cresol) and mixtures thereof. The content of the reducing agent represented by the above general formula [] used in the heat-developable photosensitive material of the present invention is determined appropriately depending on the desired properties, but is generally based on 1 mole of organic silver salt. The amount is 5 mol or less, preferably 1 mol or less, most preferably 1 mol to 10 -4 mol. Furthermore, when it is contained in combination with other reducing agents, it can be contained in the same amount as above as the total amount of reducing agents. At this time, it is preferable that the proportion of the reducing agent represented by the above general formula [] is 10% by weight or more based on the total amount of the reducing agent. Furthermore, in the heat-developable photosensitive material for electrostatic printing master of the present invention, a toning agent is used to control the color tone of the resulting image, and a toning agent is used to impart stability to the image, which is particularly important during long-term storage. A light stabilizer for preventing so-called fogging due to light during storage of heat-developable photosensitive materials before image formation and for preventing temporal changes in images due to fogging after image formation; Components such as sensitizing dyes and development accelerators may be added in necessary amounts depending on the desired properties of the heat-developable photosensitive material. Preferred binders used in the present invention, particularly those exhibiting insulating properties, include gelatin, polyvinyl butyral, polyvinyl acetate, cellulose diacetate, cellulose triacetate, cellulose acetate butyrate, polyvinyl alcohol, ethyl cellulose, methyl cellulose, benzyl Cellulose, polyvinyl acetal, cellulose propionate, cellulose acetate propionate,
Hydroxyethyl cellulose, ethyl hydroxy cellulose, carboxymethyl cellulose, polyvinyl formal, polyvinyl methyl ether,
Examples include styrene-butadiene copolymer and polymethyl methacrylate, and two or more of these compounds may be used as a mixture if necessary. The amount of these binders is determined as desired, but is usually 0.02 to 20 parts by weight, preferably 0.1 to 5 parts by weight, per 1 part by weight of the organic silver salt.
Parts by weight are preferred. Additionally, aluminum, copper, and
Metal plates such as zinc and silver or metal laminated paper,
Art paper, paper treated to prevent solvent from penetrating inside, paper treated with conductive polymer, synthetic resin film mixed with surfactant, metal, metal oxide or metal halide adhered to the surface by vapor deposition method Films such as glass or paper, synthetic resin, cellulose acetate film, polyethylene terephthalate film, polycarbonate film, and polystyrene film can be used. Insulating materials such as glass, paper, and synthetic resin may also be used. In particular, when used by wrapping it around a drum, it is preferable to use a suitable flexible metal sheet, paper, or other conductive material so that it can be wrapped around the drum. Art paper is particularly suitable as such material because of its properties as a support and its low cost. When providing a conductive layer on the surface of a synthetic resin film, paper, or other non-conductive support, either the organic silver salt layer side of the support or the side opposite to the layer may be selected depending on the purpose of use. When the conductive layer is in direct contact with the organic silver salt layer, it is preferable to select a material for forming the conductive layer that does not react with the organic silver salt. When employing a conductive support, it is generally one whose surface resistivity is smaller than the non-silver image area when forming an electrostatic printing master, that is, 10 9 Ω·cm or less, preferably 10 5 Ω·cm. Any material may be used as long as it is less than cm and does not react with the organic silver salt. In order to form an electrostatic printing master using the heat-developable photosensitive material of the present invention, in a structure in which a reducing agent layer is provided on an organic silver salt, a latent image is usually formed by imagewise exposure. It is then thermally developed to form a silver image and used as a master. Furthermore, in the case of heat-developable photosensitive materials that do not contain a reducing agent in advance, an electrostatic printing master can be formed by adding a reducing agent before or after image exposure, forming a latent image, and performing heat development. Ru. The reducing agent may be added by immersing the heat-developable photosensitive material before image exposure in a liquid containing the reducing agent at the time of use, or by applying the reducing agent before image exposure. A reducing agent may be applied by a similar treatment before post-thermal development. Alternatively, instead of the above-mentioned dipping method, a reducing agent solution dispersed in cellulose acetate etc. using an appropriate solvent may be applied onto the organic silver salt layer by methods such as brush coating, coating, doctor blade, spraying, etc. good. It is advantageous if the reducing agent layer is peeled off from the surface of the organic silver salt layer after heat development, since so-called fogging due to the action of the remaining reducing agent can be prevented. Since the heat-developable photosensitive material of the present invention has particularly excellent electrostatic properties, the use thereof has been described in detail by citing only an example of an electrostatic printing master. The uses of the material are:
It is not limited to being used in the heat-developable photosensitive material for forming the electrostatic printing master mentioned above,
It can be used as a heat-developable photosensitive material for forming a visible image by sequentially carrying out conventional image exposure and heat development, or as other optical recording materials. Hereinafter, the present invention will be explained according to examples. Example 1 25 g of 90 mol% silver behenate * , 120 g of methyl ethyl ketone and 120 g of toluene were mixed and dispersed for over 72 hours by ball milling. Thereafter, 56.5 g of polyvinyl butyral (20 wt % ethyl alcohol solution) was added and thoroughly mixed to prepare a polymer dispersion of an organic silver salt. To the thus prepared polymer dispersion were added a 200 mg/25 ml solution of calcium bromide in methyl alcohol, 2.5 g of phthalazinone, 120 mg/25 ml of mercury acetate, and a methyl alcohol solution, followed by thorough mixing.
Next, this polymer dispersion was applied onto art paper using a coating rod in a dark place so that the film thickness after drying was 8 μm to form an organic silver salt layer. [ * 90mol% silver behenate is a silver salt of organic acid.
The number of moles is divided by the number of moles of the organic acid plus the number of moles of the silver salt of the organic acid, and this value is multiplied by 100. This means the case of acid silver. The mol% of the organic acid silver salt in the following examples shall have the above meaning. ] Next, 1.5 g of the exemplified compound (1), phthalazinone
0.3 g of cellulose acetate (10 wt% acetone solution), 30 g of acetone, and 9 mg of the following compound as a sensitizing dye were mixed to prepare an overcoat layer solution. This overcoat layer solution was coated on the organic silver salt layer in a dark place so that the film thickness after drying was 4 μm to obtain a heat-developable photosensitive material for forming an electrostatic printing master (Sample 1). Next, this photosensitive material was exposed to light for 20 seconds using a tungsten light source (2500 lux) through a positive image, and then exposed to light for 130 seconds using a roller heating device.
A negative printed visible image was obtained by heat development at 50° C. for 5 seconds and was used as a master for electrostatic printing. Next, after applying a +6 KV corona discharge uniformly to the electrostatic printing master, the negatively charged toner was developed by a magnetic brush development method, and a positive toner image was obtained. When a transfer paper was placed over this toner image and the aforementioned corona discharge was applied from the transfer paper side, a clear transferred visible image was obtained. By repeating this charging and development transfer, the number of transfers increases.
Even after 1000 times or more, no deterioration was observed on the master surface, and no deterioration in the quality of the transferred image was observed. Furthermore, no deterioration of the resulting transferred image was observed even after long-term use. As a result, it was recognized that this was an excellent master for repeated printing. Furthermore, since the silver image exhibits faithful reproducibility with respect to the original image, an electrostatic charge image corresponding to the original image was formed, and it was observed that the toner image also became a faithful photographic image. When we measured the electrostatic properties of this master for electrostatic printing, we found that the charging potential difference (electrostatic contrast) between the image area (silver image area) and the non-image area (non-silver image area) was 700V, and the remaining It turns out that the potential is very small. Next, we measured the maximum blackening reflection density (Dmax) of the image area of the master.
It showed 1.65. Furthermore, when the blackening reflection density (fog density) of the non-image area on the transfer paper with the transferred image was measured, it was 0.20, which was a very small value. From the above measurements, it was found that the heat-developable photosensitive material for forming an electrostatic printing master in this example had excellent image properties and formed an excellent master for electrostatic printing that had good printing durability and was durable for practical use. Examples 2 to 5 The above-mentioned exemplified compound (1) was replaced with the above-mentioned exemplified compound (1) as a reducing agent component in the overcoat layer solution used when creating the heat-developable photosensitive material for electrostatic printing master used in the above-mentioned Example 1. Compound (1) - denoted as "A" - and 2,2
A heat-developable photosensitive material for electrostatic printing masters was prepared in the same manner except that methylenebis(6-t-butyl-P-cresol) -denoted as "B"- was used in combination at the mixing ratio shown in Table 1. It was created. This heat-developable photosensitive material was subjected to image exposure and heat development in the same manner as in Example 1 to prepare an electrostatic printing master. Next, electrostatic properties were measured using the same method. These results are shown in Table 1.
【表】
第1表から判るとおり、本発明の熱現像性感光
材料によつて優れた静電印刷マスターが作成でき
た。
実施例 6
下記に示す有機銀塩層形成組成物A及び上塗層
形成組成物Bを実施例1の手順に従つて調製し、
更にアート紙上に塗布し静電印刷マスター形成用
熱現像性感光材料とした。
組成物A:80mol%カプリン酸銀10gメチルエチ
ルケトン30g,トルエン30g
ポリビニルプチラール(10wt%エチルアル
コール溶液)60g
CaBr2 60mg
N―ブロモアセトアミド 50mg
2,3―ジヒドロキシ―5―ヒドロキシ―
1,4―フタラジンジオン1g
組成物B:前記例示化合物(2) 0.8g
酢酸セルロース(10wt%アセトン溶液)
10g
アセトン 30g
3,3′―ジエチル―2,2′―チアカルボシア
ニンアイオダイド 8mg
次に、この感光材料について実施例1と同様に
静電印刷用マスターとしての諸特性を調べたとこ
ろ、実施例1と同様に優れた静電印刷用マスター
を与える静電印刷マスター形成用熱現像性感光材
料であつた。
実施例 7
前記実施例1の静電印刷マスター用熱現像性感
光材料を作成した時に用いた前記例示化合物に代
えて、前記例示化合物(4)を用いたほかは、同様の
方法によつて熱現像性感光材料を作成してから静
電印刷マスターを調製した。これについて実施例
1と同様の方法によつて静電特性を測定したが、
ほぼ同様の結果が得られた。
前記実施例1〜7から明らかな様に、前記一般
式〔〕で示される化合物を還元剤として使用す
ることによつて、改善された静電特性が得られ
る。
本発明は、特許請求の範囲に記載した特徴を有
するものであるが、その実施態様を挙げると下記
のとおりである。
(2) 前記(c)還元剤が
である特許請求の範囲第1項記載の熱現像性感
光材料。
(3) 前記(c)還元剤が
である特許請求の範囲第1項記載の熱現像性感
光材料。
(4) 前記(c)還元剤が
である特許請求の範囲第1項記載の熱現像性感
光材料。
(5) 前記(c)還元剤が
である特許請求の範囲第1項記載の熱現像性感
光材料。
(6) 前記(c)還元剤として前記一般式〔〕で示さ
れる化合物の少なくとも1種とその他の還元剤
の少なくとも1種を含有することを特徴とする
熱現像性感光材料。
(7) 前記(c)還元剤として前記一般式〔〕で示さ
れる化合物の少なくとも1種を還元剤総量に対
して10重量%以上含有する前記第6項記載の熱
現像性感光材料。
(8) 前記その他の還元剤がアミノフエノール類、
フエニレンジアミン類、ポリヒドロキシベンゼ
ン類、アスコルビン酸類、3―ピラゾリドン
類、オキシテトロン酸類、ヒドロキシテトロン
イミド類およびレダクトン系還元剤からなる化
合物群から少なくとも1種選択した化合物であ
る前記第6項記載の熱現像性感光材料。
(9) 前記(a)有機銀塩が長鎖脂肪酸銀塩である特許
請求の範囲第1項記載の熱現像性感光材料。
(10) 前記(a)有機銀塩がベヘン酸銀である特許請求
の範囲第1項記載の熱現像性感光材料。
(11) 前記(d)結着剤が絶縁性を有した結着剤である
特許請求の範囲第1項記載の熱現像性感光材
料。
(12) 前記熱現像性感光材料が静電印刷マスター用
熱現像性感光材料である特許請求の範囲第1項
記載の熱現像性感光材料。[Table] As can be seen from Table 1, an excellent electrostatic printing master could be prepared using the heat-developable photosensitive material of the present invention. Example 6 An organic silver salt layer-forming composition A and an overcoat layer-forming composition B shown below were prepared according to the procedure of Example 1,
It was further coated on art paper to obtain a heat-developable photosensitive material for forming an electrostatic printing master. Composition A: 80mol% silver caprate 10g methyl ethyl ketone 30g, toluene 30g polyvinylbutyral (10wt% ethyl alcohol solution) 60g CaBr 2 60mg N-bromoacetamide 50mg 2,3-dihydroxy-5-hydroxy-
1,4-phthalazinedione 1g Composition B: Exemplary compound (2) 0.8g Cellulose acetate (10wt% acetone solution)
10g Acetone 30g 3,3'-diethyl-2,2'-thiacarbocyanine iodide 8mg Next, the various properties of this photosensitive material as a master for electrostatic printing were investigated in the same manner as in Example 1. Like No. 1, this was a heat-developable photosensitive material for forming an electrostatic printing master that provided an excellent electrostatic printing master. Example 7 The heat-developable photosensitive material for electrostatic printing masters of Example 1 was prepared using the same method except that the exemplified compound (4) was used in place of the exemplified compound used to create the photothermographic material for electrostatic printing masters. After creating a developable photosensitive material, an electrostatic printing master was prepared. The electrostatic properties were measured using the same method as in Example 1.
Almost similar results were obtained. As is clear from Examples 1 to 7, improved electrostatic properties can be obtained by using the compound represented by the general formula [] as a reducing agent. The present invention has the features described in the claims, and its embodiments are as follows. (2) The above (c) reducing agent is A heat-developable photosensitive material according to claim 1. (3) The above (c) reducing agent is A heat-developable photosensitive material according to claim 1. (4) The above (c) reducing agent is A heat-developable photosensitive material according to claim 1. (5) The above (c) reducing agent is A heat-developable photosensitive material according to claim 1. (6) A heat-developable photosensitive material containing at least one compound represented by the general formula [] and at least one other reducing agent as the reducing agent (c). (7) The heat-developable photosensitive material according to item 6, which contains at least one compound represented by the general formula [] as the reducing agent (c) in an amount of 10% by weight or more based on the total amount of the reducing agent. (8) The other reducing agent is aminophenols,
The compound according to item 6, which is at least one compound selected from the group consisting of phenylene diamines, polyhydroxybenzenes, ascorbic acids, 3-pyrazolidones, oxytetronic acids, hydroxytetronimides, and reductone-based reducing agents. Heat-developable photosensitive material. (9) The heat-developable photosensitive material according to claim 1, wherein the organic silver salt (a) is a long-chain fatty acid silver salt. (10) The heat-developable photosensitive material according to claim 1, wherein the organic silver salt (a) is silver behenate. (11) The heat-developable photosensitive material according to claim 1, wherein the binder (d) is an insulating binder. (12) The heat-developable photosensitive material according to claim 1, wherein the heat-developable photosensitive material is a heat-developable photosensitive material for electrostatic printing masters.
Claims (1)
性ハロゲン化銀若しくは前記(a)有機銀塩と反応さ
せてハロゲン化銀を形成しうるハロゲン化合物、
(c)還元剤および(d)結着剤からなる被覆層を単層若
しくは積層構造で設けた熱現像性感光材料におい
て、前記(c)還元剤として下記一般式〔〕で示さ
れる化合物の少なくとも1種を含有することを特
徴とする熱現像性感光材料。 一般式〔〕 (式中、R1およびR2は、第3級アルキル基を
示す。R3およびR4は、置換若しくは非置換のア
ルキル基を示す。nは、1〜4の整数である。)[Scope of Claims] 1. On a support, at least (a) an organic silver salt, (b) a photosensitive silver halide, or a halogen compound capable of reacting with the (a) organic silver salt to form a silver halide;
In a heat-developable photosensitive material in which a coating layer consisting of (c) a reducing agent and (d) a binder is provided in a single layer or a laminated structure, at least one of the compounds represented by the following general formula [] as the (c) reducing agent is used. A heat-developable photosensitive material characterized by containing one of the following. General formula [] (In the formula, R 1 and R 2 represent a tertiary alkyl group. R 3 and R 4 represent a substituted or unsubstituted alkyl group. n is an integer of 1 to 4.)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15850880A JPS5782828A (en) | 1980-11-11 | 1980-11-11 | Heat developing photosensitive material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15850880A JPS5782828A (en) | 1980-11-11 | 1980-11-11 | Heat developing photosensitive material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5782828A JPS5782828A (en) | 1982-05-24 |
JPS6147404B2 true JPS6147404B2 (en) | 1986-10-18 |
Family
ID=15673260
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP15850880A Granted JPS5782828A (en) | 1980-11-11 | 1980-11-11 | Heat developing photosensitive material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5782828A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0523787Y2 (en) * | 1987-09-25 | 1993-06-17 | ||
TWI787516B (en) * | 2018-07-19 | 2022-12-21 | 福田章 | Joint utilizing incomplete thread of male threaded portion |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0243935B1 (en) * | 1986-05-02 | 1994-07-27 | E.I. Du Pont De Nemours And Company | Improved silver-based electrostatic printing master |
ZA941088B (en) * | 1993-02-19 | 1995-09-27 | Symphar Sa | Substituted ketophosphonates the processes for their preparation and pharmaceutical compositions containing them |
-
1980
- 1980-11-11 JP JP15850880A patent/JPS5782828A/en active Granted
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0523787Y2 (en) * | 1987-09-25 | 1993-06-17 | ||
TWI787516B (en) * | 2018-07-19 | 2022-12-21 | 福田章 | Joint utilizing incomplete thread of male threaded portion |
Also Published As
Publication number | Publication date |
---|---|
JPS5782828A (en) | 1982-05-24 |
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