CA1148788A - Photographic silver halide materials containing dispersed light-absorbing merostyryl dyes - Google Patents
Photographic silver halide materials containing dispersed light-absorbing merostyryl dyesInfo
- Publication number
- CA1148788A CA1148788A CA000353167A CA353167A CA1148788A CA 1148788 A CA1148788 A CA 1148788A CA 000353167 A CA000353167 A CA 000353167A CA 353167 A CA353167 A CA 353167A CA 1148788 A CA1148788 A CA 1148788A
- Authority
- CA
- Canada
- Prior art keywords
- group
- light
- dye
- layer
- silver halide
- 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 title claims abstract description 40
- -1 silver halide Chemical class 0.000 title claims abstract description 28
- 229910052709 silver Inorganic materials 0.000 title claims abstract description 20
- 239000004332 silver Substances 0.000 title claims abstract description 20
- 239000000975 dye Substances 0.000 title description 81
- 239000000084 colloidal system Substances 0.000 claims abstract description 19
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 17
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 9
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 6
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims abstract description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 6
- 239000001257 hydrogen Substances 0.000 claims abstract description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 6
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims abstract description 5
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 claims abstract description 4
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract description 3
- 125000003118 aryl group Chemical group 0.000 claims abstract description 3
- 125000005161 aryl oxy carbonyl group Chemical group 0.000 claims abstract description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 3
- 239000000839 emulsion Substances 0.000 claims description 19
- 108010010803 Gelatin Proteins 0.000 claims description 16
- 229920000159 gelatin Polymers 0.000 claims description 16
- 239000008273 gelatin Substances 0.000 claims description 16
- 235000019322 gelatine Nutrition 0.000 claims description 16
- 235000011852 gelatine desserts Nutrition 0.000 claims description 16
- 239000011230 binding agent Substances 0.000 claims description 7
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 2
- 125000003107 substituted aryl group Chemical group 0.000 claims description 2
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 27
- 238000010521 absorption reaction Methods 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 230000009102 absorption Effects 0.000 description 13
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
- RGHHSNMVTDWUBI-UHFFFAOYSA-N 4-hydroxybenzaldehyde Chemical compound OC1=CC=C(C=O)C=C1 RGHHSNMVTDWUBI-UHFFFAOYSA-N 0.000 description 11
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- 239000004576 sand Substances 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- 238000002844 melting Methods 0.000 description 7
- 230000008018 melting Effects 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 230000000875 corresponding effect Effects 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 6
- 239000011541 reaction mixture Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 238000011282 treatment Methods 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- CUGBBQWDGCXWNB-UHFFFAOYSA-N 4-(3-methyl-5-oxo-4h-pyrazol-1-yl)benzoic acid Chemical compound O=C1CC(C)=NN1C1=CC=C(C(O)=O)C=C1 CUGBBQWDGCXWNB-UHFFFAOYSA-N 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- SMQUZDBALVYZAC-UHFFFAOYSA-N salicylaldehyde Chemical compound OC1=CC=CC=C1C=O SMQUZDBALVYZAC-UHFFFAOYSA-N 0.000 description 4
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 238000000862 absorption spectrum Methods 0.000 description 2
- 230000002180 anti-stress Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 229940125904 compound 1 Drugs 0.000 description 2
- 229940126214 compound 3 Drugs 0.000 description 2
- 229940125898 compound 5 Drugs 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- JVTZFYYHCGSXJV-UHFFFAOYSA-N isovanillin Chemical compound COC1=CC=C(C=O)C=C1O JVTZFYYHCGSXJV-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000012216 screening Methods 0.000 description 2
- IZWPGJFSBABFGL-GMFCBQQYSA-M sodium;2-[methyl-[(z)-octadec-9-enoyl]amino]ethanesulfonate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CCS([O-])(=O)=O IZWPGJFSBABFGL-GMFCBQQYSA-M 0.000 description 2
- 229940086542 triethylamine Drugs 0.000 description 2
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 2
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 2
- 235000012141 vanillin Nutrition 0.000 description 2
- 239000001043 yellow dye Substances 0.000 description 2
- ZRHUHDUEXWHZMA-UHFFFAOYSA-N 1,4-dihydropyrazol-5-one Chemical compound O=C1CC=NN1 ZRHUHDUEXWHZMA-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
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 description 1
- GAENKRKEATZTPX-UHFFFAOYSA-N 4-(3-ethoxycarbonyl-5-oxo-4h-pyrazol-1-yl)benzoic acid Chemical compound O=C1CC(C(=O)OCC)=NN1C1=CC=C(C(O)=O)C=C1 GAENKRKEATZTPX-UHFFFAOYSA-N 0.000 description 1
- OSYGMPDZJABVSF-UHFFFAOYSA-N 4-[(4-hydroxyphenyl)methylidene]-5-oxo-1-phenylpyrazole-3-carboxamide Chemical compound C1(=CC=CC=C1)N1N=C(C(C1=O)=CC1=CC=C(C=C1)O)C(N)=O OSYGMPDZJABVSF-UHFFFAOYSA-N 0.000 description 1
- DENONHJBIZGIDT-UHFFFAOYSA-N 4-[(4-hydroxyphenyl)methylidene]-5-oxo-1-phenylpyrazole-3-carboxylic acid Chemical compound OC(=O)C1=NN(C(=O)C1=CC1=CC=C(O)C=C1)C1=CC=CC=C1 DENONHJBIZGIDT-UHFFFAOYSA-N 0.000 description 1
- SUQTVLPQFFSCFL-UHFFFAOYSA-N 4-[3-ethoxycarbonyl-4-[(4-hydroxyphenyl)methylidene]-5-oxopyrazol-1-yl]benzoic acid Chemical compound C(=O)(O)C1=CC=C(C=C1)N1N=C(C(C1=O)=CC1=CC=C(C=C1)O)C(=O)OCC SUQTVLPQFFSCFL-UHFFFAOYSA-N 0.000 description 1
- STLGNICRBXPCTR-UHFFFAOYSA-N 5-oxo-1-(2,2,2-trifluoroethyl)-4h-pyrazole-3-carboxamide Chemical compound NC(=O)C1=NN(CC(F)(F)F)C(=O)C1 STLGNICRBXPCTR-UHFFFAOYSA-N 0.000 description 1
- SPFXLCCBWAJCHQ-UHFFFAOYSA-N 5-oxo-1-phenyl-4h-pyrazole-3-carboxamide Chemical compound O=C1CC(C(=O)N)=NN1C1=CC=CC=C1 SPFXLCCBWAJCHQ-UHFFFAOYSA-N 0.000 description 1
- IMZSHPUSPMOODC-UHFFFAOYSA-N 5-oxo-1-phenyl-4h-pyrazole-3-carboxylic acid Chemical compound O=C1CC(C(=O)O)=NN1C1=CC=CC=C1 IMZSHPUSPMOODC-UHFFFAOYSA-N 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 208000036366 Sensation of pressure Diseases 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- 239000001045 blue dye Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000001768 carboxy methyl 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
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 229940125782 compound 2 Drugs 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 239000007857 degradation product Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 150000002696 manganese Chemical class 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 229940087646 methanolamine Drugs 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 230000001617 migratory effect Effects 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 230000001473 noxious effect Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229940068984 polyvinyl alcohol Drugs 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical class O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000001044 red dye Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
- C09B23/0091—Methine or polymethine dyes, e.g. cyanine dyes having only one heterocyclic ring at one end of the methine chain, e.g. hemicyamines, hemioxonol
-
- 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
- G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
- G03C1/825—Photosensitive materials characterised by the base or auxiliary layers characterised by antireflection means or visible-light filtering means, e.g. antihalation
- G03C1/83—Organic dyestuffs therefor
- G03C1/832—Methine or polymethine dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Organic Chemistry (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB7922724 | 1979-06-29 | ||
GB7922724 | 1979-06-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1148788A true CA1148788A (en) | 1983-06-28 |
Family
ID=10506193
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA000353167A Expired CA1148788A (en) | 1979-06-29 | 1980-06-02 | Photographic silver halide materials containing dispersed light-absorbing merostyryl dyes |
Country Status (5)
Country | Link |
---|---|
US (1) | US4311787A (en:Method) |
EP (1) | EP0021513B1 (en:Method) |
JP (1) | JPS5612639A (en:Method) |
CA (1) | CA1148788A (en:Method) |
DE (1) | DE3067115D1 (en:Method) |
Families Citing this family (49)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0078233A1 (de) * | 1981-10-15 | 1983-05-04 | Ciba-Geigy Ag | Lichtempfindliches, Polymerbilder lieferndes Aufzeichnungsmaterial und Farbstoffe |
US4477562A (en) * | 1983-05-24 | 1984-10-16 | Minnesota Mining And Manufacturing Company | Dry strip antihalation layer for photothermographic film |
ES2014297B3 (es) * | 1986-07-08 | 1990-07-01 | Agfa-Gevaert Nv | Elemento fotografico colorante para proyeccion cinematografica. |
CA1299424C (en) * | 1986-12-23 | 1992-04-28 | Donald R. Diehl | Radiographic element exhibiting reduced crossover |
US4803150A (en) * | 1986-12-23 | 1989-02-07 | Eastman Kodak Company | Radiographic element exhibiting reduced crossover |
CA1286139C (en) * | 1986-12-23 | 1991-07-16 | Donald Richard Diehl | Filter dye for photographic element |
US4948717A (en) * | 1986-12-23 | 1990-08-14 | Eastman Kodak Company | Solid particle dye dispersions for photographic filter layers |
JP2879106B2 (ja) * | 1988-06-13 | 1999-04-05 | 富士写真フイルム株式会社 | カラー画像形成法 |
EP0351593A3 (en) * | 1988-06-30 | 1991-01-30 | Eastman Kodak Company | Light-handleable photographic element having solid particle dispersion filter dye layer |
ES2011729A6 (es) * | 1988-12-26 | 1990-02-01 | Gabas Cebollero Carlos | Tapa para espejos de parasoles de vehiculos automoviles. |
JPH02264936A (ja) * | 1989-04-06 | 1990-10-29 | Fuji Photo Film Co Ltd | X線用ハロゲン化銀写真感光材料 |
JPH02278257A (ja) * | 1989-04-20 | 1990-11-14 | Fuji Photo Film Co Ltd | 直接ポジカラー写真感光材料 |
JP2649967B2 (ja) * | 1989-04-24 | 1997-09-03 | 富士写真フイルム株式会社 | ハロゲン化銀写真感光材料 |
JP2829394B2 (ja) * | 1989-05-24 | 1998-11-25 | 富士写真フイルム株式会社 | ハロゲン化銀カラー写真感光材料 |
JP2922528B2 (ja) * | 1989-05-24 | 1999-07-26 | 富士写真フイルム株式会社 | カラー画像形成法 |
JPH0313936A (ja) * | 1989-06-12 | 1991-01-22 | Fuji Photo Film Co Ltd | ハロゲン化銀写真感光材料 |
JP2613804B2 (ja) * | 1989-06-21 | 1997-05-28 | 富士写真フイルム株式会社 | カラー画像形成方法 |
US5213954A (en) * | 1989-07-31 | 1993-05-25 | Minnesota Mining And Manufacturing Company | White light handleable negative-acting silver halide photographic elements |
JPH03100541A (ja) * | 1989-09-13 | 1991-04-25 | Fuji Photo Film Co Ltd | ハロゲン化銀写真感光材料 |
JP2579220B2 (ja) * | 1989-10-03 | 1997-02-05 | 富士写真フイルム株式会社 | ハロゲン化銀カラー写真感光材料 |
JP2627197B2 (ja) * | 1989-10-09 | 1997-07-02 | 富士写真フイルム株式会社 | ハロゲン化銀写真感光材料 |
JPH03126938A (ja) * | 1989-10-12 | 1991-05-30 | Fuji Photo Film Co Ltd | ハロゲン化銀カラー写真感光材料 |
JPH03127048A (ja) * | 1989-10-13 | 1991-05-30 | Fuji Photo Film Co Ltd | ハロゲン化銀カラー写真感光材料 |
JPH03130762A (ja) * | 1989-10-16 | 1991-06-04 | Fuji Photo Film Co Ltd | ハロゲン化銀カラー反転写真感光材料 |
JPH03130761A (ja) * | 1989-10-16 | 1991-06-04 | Fuji Photo Film Co Ltd | ハロゲン化銀カラー写真感光材料 |
JPH03135551A (ja) * | 1989-10-17 | 1991-06-10 | Fuji Photo Film Co Ltd | ハロゲン化銀カラー写真感光材料 |
JPH03131844A (ja) * | 1989-10-17 | 1991-06-05 | Fuji Photo Film Co Ltd | 直接ポジ画像形成方法 |
US5213957A (en) * | 1989-11-27 | 1993-05-25 | Fuji Photo Film Co., Ltd. | Silver halide photographic light-sensitive materials |
US5208137A (en) * | 1989-12-28 | 1993-05-04 | Konica Corporation | Silver halide photographic light-sensitive material |
JPH03210553A (ja) * | 1990-01-16 | 1991-09-13 | Fuji Photo Film Co Ltd | ハロゲン化銀写真感光材料 |
JPH03293340A (ja) * | 1990-04-11 | 1991-12-25 | Fuji Photo Film Co Ltd | ハロゲン化銀立体カラー写真感光材料およびこれを用いた立体カラー画像形成法 |
JPH0498243A (ja) * | 1990-08-17 | 1992-03-30 | Fuji Photo Film Co Ltd | ハロゲン化銀写真感光材料 |
US5262284A (en) * | 1991-07-15 | 1993-11-16 | Eastman Kodak Company | Arylidene pyrazolone coupler |
JPH07199408A (ja) * | 1991-07-22 | 1995-08-04 | Eastman Kodak Co | 写真要素用フィルター色素固体粒子分散体 |
US5275928A (en) * | 1991-11-27 | 1994-01-04 | E. I. Du Pont De Nemours And Company | Arylidene sensitizing dyes for tabular grains |
JP2767335B2 (ja) * | 1992-01-20 | 1998-06-18 | 富士写真フイルム株式会社 | ハロゲン化銀写真感光材料 |
JP2787628B2 (ja) * | 1992-01-21 | 1998-08-20 | 富士写真フイルム株式会社 | ハロゲン化銀写真感光材料 |
EP0582000A1 (en) * | 1992-08-03 | 1994-02-09 | Agfa-Gevaert N.V. | Photographic colour negative or colour intermediate film element |
EP0674227B1 (en) | 1994-03-22 | 1996-06-12 | Agfa-Gevaert N.V. | Imaging element and method for making a printing plate according to the silver salt diffusion transfer process |
EP0681209A1 (en) * | 1994-05-06 | 1995-11-08 | Agfa-Gevaert N.V. | Multilayer direct-positive photographic material and process for preparing the same |
EP0698822B1 (en) | 1994-08-22 | 1999-03-17 | Agfa-Gevaert N.V. | Lithographic printing plate precursor with a flexible support and method for making a lithographic printing plate therewith |
EP0745901B1 (en) | 1995-05-31 | 1999-03-17 | Agfa-Gevaert N.V. | A concentrated dampening solution with an improved shelf life for printing with a lithographic printing plate obtained according to the silver salt diffusion transfer process |
DE69512392T2 (de) | 1995-06-23 | 2000-04-13 | Agfa-Gevaert N.V., Mortsel | Bildelement und Verfahren zur Herstellung lithographischen Druckplatten nach dem Silbersalz-Diffusionübertragungsverfahren |
US5834173A (en) * | 1995-12-22 | 1998-11-10 | Eastman Kodak Company | Filter dyes for photographic elements |
EP0768569B1 (en) * | 1995-10-16 | 2003-04-02 | Agfa-Gevaert | New class of yellow dyes for use in photographic materials |
EP0774693B1 (en) | 1995-11-16 | 2000-05-24 | Agfa-Gevaert N.V. | A method for making by phototypesetting a lithographic printing plate according to the silver salt diffusion transfer process |
EP0779554A1 (en) | 1995-12-14 | 1997-06-18 | Agfa-Gevaert N.V. | A correcting liquid for a silver imaged lithographic printing plate |
EP0790532B1 (en) | 1996-02-14 | 2000-07-05 | Agfa-Gevaert N.V. | A method for making a lithographic printing plate according to the silver salt diffusion transfer process |
JP4342373B2 (ja) * | 2004-04-30 | 2009-10-14 | 東京応化工業株式会社 | 凸版印刷用感光性印刷原版、凸版印刷版の製造方法、および該製造方法用遮光インク |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB191026677A (en) * | 1910-03-14 | 1911-02-16 | Philip Arthur Newton | Manufacture and Production of New Dyestuffs. |
FR1378648A (fr) * | 1963-01-04 | 1964-11-13 | Ferrania Spa | Procédé de préparation de couches colorées antihalo et filtrantes pour matière sensible photographique |
FR1350311A (fr) * | 1963-03-07 | 1964-01-24 | Agfa Ag | Procédé de fabrication de couches antihalo |
US3382075A (en) * | 1964-12-08 | 1968-05-07 | Eastman Kodak Co | Supersensitization of benzylidene dyes in silver halide emulsions |
DE1472789A1 (de) * | 1965-12-10 | 1969-01-23 | Agfa Gevaert Ag | Gelbe Lichthofschutz- und Filterfarbstoffe fuer photographische Materialien |
GB1167026A (en) * | 1966-10-04 | 1969-10-15 | Agfa Gevaert Nv | Coloured Colloid Materials |
GB1210252A (en) * | 1967-06-16 | 1970-10-28 | Agfa Gevaert Nv | Methine dyes and colloid layers containing them |
GB1210253A (en) * | 1967-06-16 | 1970-10-28 | Agfa Gevaert Nv | Coloured colloid materials |
GB1426179A (en) * | 1972-06-22 | 1976-02-25 | Agfa Gevaert | Dyes and their use in photographic antihalation layers |
JPS513623A (en) * | 1974-06-28 | 1976-01-13 | Fuji Photo Film Co Ltd | Senryoofukumu harogenkaginshashinkankozairyo |
JPS5110927A (en) * | 1974-07-17 | 1976-01-28 | Fuji Photo Film Co Ltd | Senryooganjusuru harogenkaginshashinkankozairyo |
-
1980
- 1980-06-02 CA CA000353167A patent/CA1148788A/en not_active Expired
- 1980-06-11 US US06/158,450 patent/US4311787A/en not_active Expired - Lifetime
- 1980-06-13 DE DE8080200554T patent/DE3067115D1/de not_active Expired
- 1980-06-13 EP EP80200554A patent/EP0021513B1/en not_active Expired
- 1980-06-19 JP JP8339380A patent/JPS5612639A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
DE3067115D1 (en) | 1984-04-26 |
JPS5612639A (en) | 1981-02-07 |
JPH0352616B2 (en:Method) | 1991-08-12 |
US4311787A (en) | 1982-01-19 |
EP0021513A1 (en) | 1981-01-07 |
EP0021513B1 (en) | 1984-03-21 |
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