CA2328695A1 - Imaging element containing a blocked photographically useful compound - Google Patents
Imaging element containing a blocked photographically useful compound Download PDFInfo
- Publication number
- CA2328695A1 CA2328695A1 CA002328695A CA2328695A CA2328695A1 CA 2328695 A1 CA2328695 A1 CA 2328695A1 CA 002328695 A CA002328695 A CA 002328695A CA 2328695 A CA2328695 A CA 2328695A CA 2328695 A1 CA2328695 A1 CA 2328695A1
- Authority
- CA
- Canada
- Prior art keywords
- image
- silver
- group
- substituted
- groups
- 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.)
- Abandoned
Links
- 238000003384 imaging method Methods 0.000 title claims abstract description 53
- 150000001875 compounds Chemical class 0.000 title claims abstract description 45
- 229910052709 silver Inorganic materials 0.000 claims description 108
- 239000004332 silver Substances 0.000 claims description 108
- -1 silver halide Chemical class 0.000 claims description 79
- 238000000034 method Methods 0.000 claims description 65
- 239000003795 chemical substances by application Substances 0.000 claims description 35
- 125000000217 alkyl group Chemical group 0.000 claims description 29
- 125000003118 aryl group Chemical group 0.000 claims description 26
- 238000011161 development Methods 0.000 claims description 26
- 229910052799 carbon Inorganic materials 0.000 claims description 22
- 229910052717 sulfur Inorganic materials 0.000 claims description 22
- 230000003595 spectral effect Effects 0.000 claims description 20
- 229910052760 oxygen Inorganic materials 0.000 claims description 19
- 230000015572 biosynthetic process Effects 0.000 claims description 17
- 239000003381 stabilizer Substances 0.000 claims description 17
- 125000000623 heterocyclic group Chemical group 0.000 claims description 16
- 229910052739 hydrogen Inorganic materials 0.000 claims description 16
- 239000001257 hydrogen Substances 0.000 claims description 16
- 239000000126 substance Substances 0.000 claims description 16
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 14
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 14
- 239000011593 sulfur Chemical group 0.000 claims description 14
- 239000002243 precursor Substances 0.000 claims description 13
- 239000001301 oxygen Substances 0.000 claims description 11
- 238000007639 printing Methods 0.000 claims description 11
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 10
- 239000003112 inhibitor Substances 0.000 claims description 10
- 229910052757 nitrogen Inorganic materials 0.000 claims description 10
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 9
- 229910052736 halogen Inorganic materials 0.000 claims description 9
- 150000002367 halogens Chemical group 0.000 claims description 9
- 239000007844 bleaching agent Substances 0.000 claims description 7
- 150000001721 carbon Chemical class 0.000 claims description 6
- 239000004848 polyfunctional curative Substances 0.000 claims description 6
- 239000004094 surface-active agent Substances 0.000 claims description 6
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims description 5
- NVXLIZQNSVLKPO-UHFFFAOYSA-N Glucosereductone Chemical compound O=CC(O)C=O NVXLIZQNSVLKPO-UHFFFAOYSA-N 0.000 claims description 5
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
- 125000005647 linker group Chemical group 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 5
- FOIXSVOLVBLSDH-UHFFFAOYSA-N Silver ion Chemical compound [Ag+] FOIXSVOLVBLSDH-UHFFFAOYSA-N 0.000 claims description 4
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 4
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 claims description 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 4
- 125000006575 electron-withdrawing group Chemical group 0.000 claims description 4
- 238000010534 nucleophilic substitution reaction Methods 0.000 claims description 4
- CYFLXLSBHQBMFT-UHFFFAOYSA-N sulfamoxole Chemical group O1C(C)=C(C)N=C1NS(=O)(=O)C1=CC=C(N)C=C1 CYFLXLSBHQBMFT-UHFFFAOYSA-N 0.000 claims description 4
- WSNMPAVSZJSIMT-UHFFFAOYSA-N COc1c(C)c2COC(=O)c2c(O)c1CC(O)C1(C)CCC(=O)O1 Chemical compound COc1c(C)c2COC(=O)c2c(O)c1CC(O)C1(C)CCC(=O)O1 WSNMPAVSZJSIMT-UHFFFAOYSA-N 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 239000012992 electron transfer agent Substances 0.000 claims description 3
- 238000012805 post-processing Methods 0.000 claims description 3
- 239000006097 ultraviolet radiation absorber Substances 0.000 claims description 3
- 229940090898 Desensitizer Drugs 0.000 claims description 2
- 125000005422 alkyl sulfonamido group Chemical group 0.000 claims description 2
- 238000003776 cleavage reaction Methods 0.000 claims description 2
- 239000008139 complexing agent Substances 0.000 claims description 2
- 150000002373 hemiacetals Chemical class 0.000 claims description 2
- 238000007781 pre-processing Methods 0.000 claims description 2
- 230000027756 respiratory electron transport chain Effects 0.000 claims description 2
- 125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 claims description 2
- 238000006276 transfer reaction Methods 0.000 claims description 2
- 150000002431 hydrogen Chemical group 0.000 claims 5
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 claims 2
- 239000006260 foam Substances 0.000 claims 1
- 239000010410 layer Substances 0.000 description 126
- 239000000839 emulsion Substances 0.000 description 96
- 239000000975 dye Substances 0.000 description 91
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 66
- 238000012545 processing Methods 0.000 description 64
- 238000000576 coating method Methods 0.000 description 60
- 239000011248 coating agent Substances 0.000 description 44
- 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 description 44
- 239000000243 solution Substances 0.000 description 42
- 108010010803 Gelatin Proteins 0.000 description 41
- 239000008273 gelatin Substances 0.000 description 41
- 229920000159 gelatin Polymers 0.000 description 41
- 235000019322 gelatine Nutrition 0.000 description 41
- 235000011852 gelatine desserts Nutrition 0.000 description 41
- 238000011160 research Methods 0.000 description 34
- 239000002019 doping agent Substances 0.000 description 32
- 239000006185 dispersion Substances 0.000 description 30
- 230000018109 developmental process Effects 0.000 description 25
- 239000000463 material Substances 0.000 description 24
- 230000008569 process Effects 0.000 description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
- 230000000052 comparative effect Effects 0.000 description 17
- 238000010438 heat treatment Methods 0.000 description 17
- 230000035945 sensitivity Effects 0.000 description 17
- 238000012360 testing method Methods 0.000 description 16
- 239000003638 chemical reducing agent Substances 0.000 description 14
- 230000000875 corresponding effect Effects 0.000 description 13
- WKEDVNSFRWHDNR-UHFFFAOYSA-N salicylanilide Chemical compound OC1=CC=CC=C1C(=O)NC1=CC=CC=C1 WKEDVNSFRWHDNR-UHFFFAOYSA-N 0.000 description 13
- 229950000975 salicylanilide Drugs 0.000 description 13
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 239000000084 colloidal system Substances 0.000 description 12
- 230000001965 increasing effect Effects 0.000 description 12
- 239000011229 interlayer Substances 0.000 description 12
- 239000000203 mixture Substances 0.000 description 12
- 206010070834 Sensitisation Diseases 0.000 description 11
- 229910052770 Uranium Inorganic materials 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 11
- 230000008313 sensitization Effects 0.000 description 11
- 238000012546 transfer Methods 0.000 description 11
- IBWXIFXUDGADCV-UHFFFAOYSA-N 2h-benzotriazole;silver Chemical compound [Ag].C1=CC=C2NN=NC2=C1 IBWXIFXUDGADCV-UHFFFAOYSA-N 0.000 description 10
- 239000012190 activator Substances 0.000 description 10
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 10
- 238000003860 storage Methods 0.000 description 10
- 230000009466 transformation Effects 0.000 description 10
- ZBHBIODEONVIMN-UHFFFAOYSA-N 1-phenyl-2h-tetrazole-5-thione;silver Chemical compound [Ag].S=C1N=NNN1C1=CC=CC=C1 ZBHBIODEONVIMN-UHFFFAOYSA-N 0.000 description 9
- 230000009102 absorption Effects 0.000 description 9
- 238000010521 absorption reaction Methods 0.000 description 9
- 125000004432 carbon atom Chemical group C* 0.000 description 9
- 239000003086 colorant Substances 0.000 description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 9
- 239000011159 matrix material Substances 0.000 description 9
- 229920000139 polyethylene terephthalate Polymers 0.000 description 9
- 239000005020 polyethylene terephthalate Substances 0.000 description 9
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 8
- 235000011941 Tilia x europaea Nutrition 0.000 description 8
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 8
- 239000002253 acid Substances 0.000 description 8
- 230000000903 blocking effect Effects 0.000 description 8
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 8
- 239000012153 distilled water Substances 0.000 description 8
- 239000004571 lime Substances 0.000 description 8
- 230000005855 radiation Effects 0.000 description 8
- 125000001424 substituent group Chemical group 0.000 description 8
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 7
- 230000005540 biological transmission Effects 0.000 description 7
- 238000010276 construction Methods 0.000 description 7
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- 230000004044 response Effects 0.000 description 7
- 150000003378 silver Chemical class 0.000 description 7
- 238000007725 thermal activation Methods 0.000 description 7
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 6
- 230000006870 function Effects 0.000 description 6
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 6
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- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 5
- 238000007792 addition Methods 0.000 description 5
- 239000002585 base Substances 0.000 description 5
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
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- 230000000269 nucleophilic effect Effects 0.000 description 5
- 150000004989 p-phenylenediamines Chemical class 0.000 description 5
- 229910001961 silver nitrate Inorganic materials 0.000 description 5
- 238000011282 treatment Methods 0.000 description 5
- GGZHVNZHFYCSEV-UHFFFAOYSA-N 1-Phenyl-5-mercaptotetrazole Chemical compound SC1=NN=NN1C1=CC=CC=C1 GGZHVNZHFYCSEV-UHFFFAOYSA-N 0.000 description 4
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
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- 239000012964 benzotriazole Substances 0.000 description 4
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 230000002829 reductive effect Effects 0.000 description 4
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 4
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- 235000021357 Behenic acid Nutrition 0.000 description 3
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 3
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- NEAQRZUHTPSBBM-UHFFFAOYSA-N 2-hydroxy-3,3-dimethyl-7-nitro-4h-isoquinolin-1-one Chemical class C1=C([N+]([O-])=O)C=C2C(=O)N(O)C(C)(C)CC2=C1 NEAQRZUHTPSBBM-UHFFFAOYSA-N 0.000 description 2
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- CZLCEPVHPYKDPJ-UHFFFAOYSA-N guanidine;2,2,2-trichloroacetic acid Chemical compound NC(N)=N.OC(=O)C(Cl)(Cl)Cl CZLCEPVHPYKDPJ-UHFFFAOYSA-N 0.000 description 2
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- YRSQDSCQMOUOKO-KVVVOXFISA-M silver;(z)-octadec-9-enoate Chemical compound [Ag+].CCCCCCCC\C=C/CCCCCCCC([O-])=O YRSQDSCQMOUOKO-KVVVOXFISA-M 0.000 description 1
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- LTYHQUJGIQUHMS-UHFFFAOYSA-M silver;hexadecanoate Chemical compound [Ag+].CCCCCCCCCCCCCCCC([O-])=O LTYHQUJGIQUHMS-UHFFFAOYSA-M 0.000 description 1
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- BBMHARZCALWXSL-UHFFFAOYSA-M sodium dihydrogenphosphate monohydrate Chemical compound O.[Na+].OP(O)([O-])=O BBMHARZCALWXSL-UHFFFAOYSA-M 0.000 description 1
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- NHQVTOYJPBRYNG-UHFFFAOYSA-M sodium;2,4,7-tri(propan-2-yl)naphthalene-1-sulfonate Chemical compound [Na+].CC(C)C1=CC(C(C)C)=C(S([O-])(=O)=O)C2=CC(C(C)C)=CC=C21 NHQVTOYJPBRYNG-UHFFFAOYSA-M 0.000 description 1
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Classifications
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- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/305—Substances liberating photographically active agents, e.g. development-inhibiting releasing couplers
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- G03C1/00—Photosensitive materials
- G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
- G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
- G03C1/42—Developers or their precursors
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- G03C1/00—Photosensitive materials
- G03C1/494—Silver salt compositions other than silver halide emulsions; Photothermographic systems ; Thermographic systems using noble metal compounds
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- 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
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- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/305—Substances liberating photographically active agents, e.g. development-inhibiting releasing couplers
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- 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
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- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/392—Additives
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- 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
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/407—Development processes or agents therefor
- G03C7/413—Developers
- G03C7/4136—Developers p-Phenylenediamine or derivatives thereof
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
- Plural Heterocyclic Compounds (AREA)
- Projection-Type Copiers In General (AREA)
- Photographic Developing Apparatuses (AREA)
- Color Television Image Signal Generators (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/475,703 | 1999-12-30 | ||
| US09/475,703 US6756192B1 (en) | 1999-12-30 | 1999-12-30 | Imaging element containing a blocked photographically useful compound |
| US09/614,035 | 2000-07-11 | ||
| US09/614,035 US6759187B1 (en) | 1999-12-30 | 2000-07-11 | Imaging element containing a blocked photographically useful compound |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2328695A1 true CA2328695A1 (en) | 2001-06-30 |
Family
ID=27044899
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002328695A Abandoned CA2328695A1 (en) | 1999-12-30 | 2000-12-15 | Imaging element containing a blocked photographically useful compound |
Country Status (7)
| Country | Link |
|---|---|
| EP (2) | EP1113326A3 (de) |
| JP (1) | JP2001242605A (de) |
| KR (1) | KR20010082583A (de) |
| CN (1) | CN1301990A (de) |
| BR (1) | BR0010438A (de) |
| CA (1) | CA2328695A1 (de) |
| TW (1) | TW588213B (de) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6790569B2 (en) * | 2000-06-13 | 2004-09-14 | Eastman Kodak Company | Color photothermographic elements comprising phenolic thermal solvents |
| JP2003043648A (ja) | 2001-05-23 | 2003-02-13 | Fuji Photo Film Co Ltd | ハロゲン化銀写真感光材料及びそれを用いた画像形成方法 |
| US6645711B2 (en) | 2001-07-18 | 2003-11-11 | Fuji Photo Film Co., Ltd. | Silver halide photographic light-sensitive material |
| US6531271B1 (en) * | 2001-08-16 | 2003-03-11 | Eastman Kodak Company | Color photographic element comprising a multifunctional dye-forming coupler |
| US6497999B1 (en) * | 2001-11-21 | 2002-12-24 | Eastman Kodak Company | Method of passivating silver donors in photothermographic systems and imaging elements made thereby |
| US6576411B1 (en) * | 2001-11-21 | 2003-06-10 | Eastman Kodak Company | Method of passivating a silver donor with a dye and photothermographic systems made thereby |
| USD763730S1 (en) | 2014-10-13 | 2016-08-16 | Robert Nielsen | Button cover with a clasp |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5814671B2 (ja) * | 1977-05-02 | 1983-03-22 | 富士写真フイルム株式会社 | カラ−写真感光材料 |
| JPS5849944A (ja) * | 1981-09-04 | 1983-03-24 | Konishiroku Photo Ind Co Ltd | カラ−写真感光材料 |
| JPS5895344A (ja) * | 1981-11-16 | 1983-06-06 | Konishiroku Photo Ind Co Ltd | 画像形成処理方法 |
| JPS59111636A (ja) * | 1982-12-17 | 1984-06-27 | Fuji Photo Film Co Ltd | 熱現像カラー感光材料およびそれを用いたカラー画像形成方法 |
| JPS61250636A (ja) * | 1985-04-30 | 1986-11-07 | Fuji Photo Film Co Ltd | 熱現像感光材料 |
| JPS62131253A (ja) * | 1985-12-03 | 1987-06-13 | Fuji Photo Film Co Ltd | 画像形成方法 |
| JPH083616B2 (ja) * | 1986-11-13 | 1996-01-17 | 富士写真フイルム株式会社 | カラ−画像形成方法 |
| US5773560A (en) * | 1996-07-25 | 1998-06-30 | Fuji Photo Film Co., Ltd. | Silver halide color photographic light-sensitive material and color image forming method |
-
2000
- 2000-12-15 JP JP2000382141A patent/JP2001242605A/ja active Pending
- 2000-12-15 EP EP00311241A patent/EP1113326A3/de not_active Withdrawn
- 2000-12-15 BR BR0010438-8A patent/BR0010438A/pt not_active IP Right Cessation
- 2000-12-15 EP EP00311239A patent/EP1113316A3/de not_active Withdrawn
- 2000-12-15 CA CA002328695A patent/CA2328695A1/en not_active Abandoned
- 2000-12-15 CN CN00135984A patent/CN1301990A/zh active Pending
- 2000-12-15 KR KR1020000077219A patent/KR20010082583A/ko not_active Application Discontinuation
- 2000-12-15 TW TW089126841A patent/TW588213B/zh not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| JP2001242605A (ja) | 2001-09-07 |
| EP1113316A2 (de) | 2001-07-04 |
| CN1301990A (zh) | 2001-07-04 |
| EP1113316A3 (de) | 2001-08-29 |
| TW588213B (en) | 2004-05-21 |
| EP1113326A2 (de) | 2001-07-04 |
| EP1113326A3 (de) | 2001-08-29 |
| BR0010438A (pt) | 2002-06-25 |
| KR20010082583A (ko) | 2001-08-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Dead |