DE1147845B - Farbentwickler fuer die Umkehrfarbentwicklung von photographischem Material - Google Patents
Farbentwickler fuer die Umkehrfarbentwicklung von photographischem MaterialInfo
- Publication number
- DE1147845B DE1147845B DEE23468A DEE0023468A DE1147845B DE 1147845 B DE1147845 B DE 1147845B DE E23468 A DEE23468 A DE E23468A DE E0023468 A DEE0023468 A DE E0023468A DE 1147845 B DE1147845 B DE 1147845B
- Authority
- DE
- Germany
- Prior art keywords
- color
- developer
- dithia
- thioether
- och
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000000463 material Substances 0.000 title claims description 23
- -1 ion compound Chemical class 0.000 claims description 51
- 150000003568 thioethers Chemical class 0.000 claims description 22
- 150000001875 compounds Chemical class 0.000 claims description 20
- 239000000243 solution Substances 0.000 claims description 7
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 125000004434 sulfur atom Chemical group 0.000 claims description 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 4
- 230000015572 biosynthetic process Effects 0.000 claims description 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 239000012670 alkaline solution Substances 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims 2
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims 1
- YZCKVEUIGOORGS-IGMARMGPSA-N Protium Chemical compound [1H] YZCKVEUIGOORGS-IGMARMGPSA-N 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 239000000975 dye Substances 0.000 claims 1
- 210000003608 fece Anatomy 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 239000001044 red dye Substances 0.000 claims 1
- 239000000839 emulsion Substances 0.000 description 16
- 239000004332 silver Substances 0.000 description 16
- 229910052709 silver Inorganic materials 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 238000000034 method Methods 0.000 description 10
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 9
- 239000000203 mixture Substances 0.000 description 8
- JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 8
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 8
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 6
- FZERHIULMFGESH-UHFFFAOYSA-N N-phenylacetamide Chemical compound CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 description 6
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 5
- 235000019982 sodium hexametaphosphate Nutrition 0.000 description 5
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- MQRJBSHKWOFOGF-UHFFFAOYSA-L disodium;carbonate;hydrate Chemical compound O.[Na+].[Na+].[O-]C([O-])=O MQRJBSHKWOFOGF-UHFFFAOYSA-L 0.000 description 4
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 4
- 229940076133 sodium carbonate monohydrate Drugs 0.000 description 4
- 235000010265 sodium sulphite Nutrition 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 229960001413 acetanilide Drugs 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- QPILZZVXGUNELN-UHFFFAOYSA-M sodium;4-amino-5-hydroxynaphthalene-2,7-disulfonate;hydron Chemical compound [Na+].OS(=O)(=O)C1=CC(O)=C2C(N)=CC(S([O-])(=O)=O)=CC2=C1 QPILZZVXGUNELN-UHFFFAOYSA-M 0.000 description 3
- XBTWVJKPQPQTDW-UHFFFAOYSA-N 4-n,4-n-diethyl-2-methylbenzene-1,4-diamine Chemical compound CCN(CC)C1=CC=C(N)C(C)=C1 XBTWVJKPQPQTDW-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- OSVMTWJCGUFAOD-KZQROQTASA-N formestane Chemical compound O=C1CC[C@]2(C)[C@H]3CC[C@](C)(C(CC4)=O)[C@@H]4[C@@H]3CCC2=C1O OSVMTWJCGUFAOD-KZQROQTASA-N 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 150000004989 p-phenylenediamines Chemical class 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- SSOLNOMRVKKSON-UHFFFAOYSA-N proguanil Chemical compound CC(C)\N=C(/N)N=C(N)NC1=CC=C(Cl)C=C1 SSOLNOMRVKKSON-UHFFFAOYSA-N 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- RWHXMBDIUHFFST-UHFFFAOYSA-N (3-aminophenyl)-(5-chloro-2-hydroxy-4-methylphenyl)methanone Chemical compound NC=1C=C(C(=O)C2=C(C=C(C(=C2)Cl)C)O)C=CC1 RWHXMBDIUHFFST-UHFFFAOYSA-N 0.000 description 1
- MHBPHWAIYZPHMO-UHFFFAOYSA-N 1,2-bis[2-(2-methoxyethylsulfanyl)ethoxy]ethane Chemical compound COCCSCCOCCOCCSCCOC MHBPHWAIYZPHMO-UHFFFAOYSA-N 0.000 description 1
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
- LDUQHYORSYOFBS-UHFFFAOYSA-N 2-(4-nitrophenoxy)-n-[5-oxo-1-(2,4,6-trichlorophenyl)-4h-pyrazol-3-yl]acetamide Chemical compound C1=CC([N+](=O)[O-])=CC=C1OCC(=O)NC1=NN(C=2C(=CC(Cl)=CC=2Cl)Cl)C(=O)C1 LDUQHYORSYOFBS-UHFFFAOYSA-N 0.000 description 1
- ADIYXAJQYBGPQB-UHFFFAOYSA-N 2-[2-[2-[2-(2-hydroxyethylsulfanyl)ethoxy]ethoxy]ethylsulfanyl]ethanol Chemical compound OCCSCCOCCOCCSCCO ADIYXAJQYBGPQB-UHFFFAOYSA-N 0.000 description 1
- JIJWGPUMOGBVMQ-UHFFFAOYSA-N 2-[3-(2-hydroxyethylsulfanyl)propylsulfanyl]ethanol Chemical compound OCCSCCCSCCO JIJWGPUMOGBVMQ-UHFFFAOYSA-N 0.000 description 1
- TUWUPOYDYIRWEI-UHFFFAOYSA-N 2-[6-(2-hydroxyethylsulfanyl)hexylsulfanyl]ethanol Chemical compound OCCSCCCCCCSCCO TUWUPOYDYIRWEI-UHFFFAOYSA-N 0.000 description 1
- SYTJKDNBEJIPID-UHFFFAOYSA-N 2-methoxyethyl 2-[2-[2-[2-(2-methoxyethoxy)-2-oxoethyl]sulfanylethoxy]ethylsulfanyl]acetate Chemical compound COCCOC(CSCCOCCSCC(OCCOC)=O)=O SYTJKDNBEJIPID-UHFFFAOYSA-N 0.000 description 1
- JKRVYGQSVNOXEC-UHFFFAOYSA-N 2-methoxyethyl 2-[2-[2-[2-[2-(2-methoxyethoxy)-2-oxoethyl]sulfanylethoxy]ethoxy]ethylsulfanyl]acetate Chemical compound COCCOC(CSCCOCCOCCSCC(OCCOC)=O)=O JKRVYGQSVNOXEC-UHFFFAOYSA-N 0.000 description 1
- OHNQVRIYXBIAPC-UHFFFAOYSA-N 2-phenoxy-N-phenylheptanamide Chemical compound C(CCCC)C(C(=O)NC1=CC=CC=C1)OC1=CC=CC=C1 OHNQVRIYXBIAPC-UHFFFAOYSA-N 0.000 description 1
- GHJPFWSRWXSALN-UHFFFAOYSA-N 3-(2-ethoxyethylsulfanyl)-N-[[3-(2-ethoxyethylsulfanyl)propanoylamino]methyl]propanamide Chemical compound CCOCCSCCC(NCNC(CCSCCOCC)=O)=O GHJPFWSRWXSALN-UHFFFAOYSA-N 0.000 description 1
- ANDMAVJOJNLFBS-UHFFFAOYSA-N 3-[3-(3-hydroxypropylsulfanyl)propylsulfanyl]propan-1-ol Chemical compound OCCCSCCCSCCCO ANDMAVJOJNLFBS-UHFFFAOYSA-N 0.000 description 1
- HHTWEFDDQAXMGO-UHFFFAOYSA-N 3-[5-(3-hydroxypropylsulfanyl)pentylsulfanyl]propan-1-ol Chemical compound OCCCSCCCCCSCCCO HHTWEFDDQAXMGO-UHFFFAOYSA-N 0.000 description 1
- QMYGFTJCQFEDST-UHFFFAOYSA-N 3-methoxybutyl acetate Chemical group COC(C)CCOC(C)=O QMYGFTJCQFEDST-UHFFFAOYSA-N 0.000 description 1
- COXDFEIOEQQVQK-UHFFFAOYSA-N 4-[(4-methoxyphenyl)diazenyl]-1,4-dihydropyrazol-5-one Chemical compound C1=CC(OC)=CC=C1N=NC1C(=O)NN=C1 COXDFEIOEQQVQK-UHFFFAOYSA-N 0.000 description 1
- MFDGLFSVMAMZSZ-UHFFFAOYSA-N 4-[3-(4-hydroxybutylsulfanyl)propylsulfanyl]butan-1-ol Chemical compound OCCCCSCCCSCCCCO MFDGLFSVMAMZSZ-UHFFFAOYSA-N 0.000 description 1
- DBGAYFFTZXJZFB-UHFFFAOYSA-N 4-[4-(4-hydroxybutylsulfanyl)butylsulfanyl]butan-1-ol Chemical compound C(CCCSCCCCSCCCCO)O DBGAYFFTZXJZFB-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
- SZEYYLKLVPYMFA-UHFFFAOYSA-N 5-[6-(5-hydroxypentylsulfanyl)hexylsulfanyl]pentan-1-ol Chemical compound OCCCCCSCCCCCCSCCCCCO SZEYYLKLVPYMFA-UHFFFAOYSA-N 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical group C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- GGXJJTBCTDTTRU-UHFFFAOYSA-N N-(5-chloro-2-hydroxy-4-methylphenyl)-2-phenylacetamide Chemical compound C1(=CC=CC=C1)CC(=O)NC1=C(C=C(C(=C1)Cl)C)O GGXJJTBCTDTTRU-UHFFFAOYSA-N 0.000 description 1
- OAKVCEDLHKIGFA-UHFFFAOYSA-N N-(5-chloro-2-hydroxy-4-methylphenyl)-4-nitrobenzamide Chemical compound [N+](=O)([O-])C1=CC=C(C(=O)NC2=C(C=C(C(=C2)Cl)C)O)C=C1 OAKVCEDLHKIGFA-UHFFFAOYSA-N 0.000 description 1
- OAWPBBBROGQRON-UHFFFAOYSA-N N-[5-benzoyl-2-[(4-methylphenyl)-(3-phenylpropyl)sulfamoyl]phenyl]acetamide Chemical compound C(C1=CC=CC=C1)(=O)C1=CC(=C(C=C1)S(=O)(=O)N(C1=CC=C(C=C1)C)CCCC1=CC=CC=C1)NC(=O)C OAWPBBBROGQRON-UHFFFAOYSA-N 0.000 description 1
- GXOHTEPVKSONOK-UHFFFAOYSA-N N-acetyl-4-ethoxy-N-(4-sulfamoylphenyl)benzamide Chemical compound C(C)OC1=CC=C(C(=O)N(C(=O)C)C2=CC=C(C=C2)S(=O)(=O)N)C=C1 GXOHTEPVKSONOK-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 description 1
- 125000004423 acyloxy group Chemical group 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 125000000043 benzamido group Chemical group [H]N([*])C(=O)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- 229960003328 benzoyl peroxide Drugs 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 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
- 159000000011 group IA salts Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 description 1
- MIROIROPBNMABJ-UHFFFAOYSA-N n-(2-hydroxy-4,6-dimethylphenyl)benzamide Chemical compound OC1=CC(C)=CC(C)=C1NC(=O)C1=CC=CC=C1 MIROIROPBNMABJ-UHFFFAOYSA-N 0.000 description 1
- NOTGPOHVOYWBLO-UHFFFAOYSA-N n-(5-chloro-2-hydroxy-4-methylphenyl)acetamide Chemical compound CC(=O)NC1=CC(Cl)=C(C)C=C1O NOTGPOHVOYWBLO-UHFFFAOYSA-N 0.000 description 1
- LEHBTJSUTDNRHE-UHFFFAOYSA-N n-(5-chloro-2-hydroxy-4-methylphenyl)benzamide Chemical compound C1=C(Cl)C(C)=CC(O)=C1NC(=O)C1=CC=CC=C1 LEHBTJSUTDNRHE-UHFFFAOYSA-N 0.000 description 1
- VSAXIWAOLMRRGF-UHFFFAOYSA-N n-[2,4-bis(2-methylbutan-2-yl)phenoxy]-n-(3,5-dichloro-2-hydroxy-4-methylphenyl)acetamide Chemical compound CCC(C)(C)C1=CC(C(C)(C)CC)=CC=C1ON(C(C)=O)C1=CC(Cl)=C(C)C(Cl)=C1O VSAXIWAOLMRRGF-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 150000004986 phenylenediamines Chemical class 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 150000003142 primary aromatic amines Chemical class 0.000 description 1
- 230000001235 sensitizing effect Effects 0.000 description 1
- 229940001593 sodium carbonate Drugs 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- NVIFVTYDZMXWGX-UHFFFAOYSA-N sodium metaborate Chemical compound [Na+].[O-]B=O NVIFVTYDZMXWGX-UHFFFAOYSA-N 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- PODWXQQNRWNDGD-UHFFFAOYSA-L sodium thiosulfate pentahydrate Chemical compound O.O.O.O.O.[Na+].[Na+].[O-]S([S-])(=O)=O PODWXQQNRWNDGD-UHFFFAOYSA-L 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 239000011593 sulfur Chemical group 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 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
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
- Y10S430/145—Infrared
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
- Y10S430/167—X-ray
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US137041A US3201242A (en) | 1961-09-11 | 1961-09-11 | Accelerators for reversal color development |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1147845B true DE1147845B (de) | 1963-04-25 |
Family
ID=22475561
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEE23468A Pending DE1147845B (de) | 1961-09-11 | 1962-09-01 | Farbentwickler fuer die Umkehrfarbentwicklung von photographischem Material |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US3201242A (en, 2012) |
| BE (1) | BE622218A (en, 2012) |
| DE (1) | DE1147845B (en, 2012) |
| GB (2) | GB1020032A (en, 2012) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4254919A (en) * | 1980-05-12 | 1981-03-10 | Polaroid Corporation | Method of loading film cassette |
| US4960683A (en) * | 1987-06-29 | 1990-10-02 | Fuji Photo Film Co., Ltd. | Method for processing a black-and-white photosensitive material |
| EP0704757A1 (en) | 1994-09-29 | 1996-04-03 | Konica Corporation | A silver halide photographic light sensitive material |
| EP0777150A1 (en) | 1995-11-29 | 1997-06-04 | Konica Corporation | Developing composition for silver halide photographic light sensitive material |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1129085A (en) * | 1965-02-24 | 1968-10-02 | Ilford Ltd | Photographic silver halide materials and the development thereof |
| US3581146A (en) * | 1969-07-29 | 1971-05-25 | Alan E Hill | Ballast for a plurality of parallel gaseous discharges |
| JPS5763530A (en) * | 1980-10-03 | 1982-04-17 | Fuji Photo Film Co Ltd | Method of development processing of color photographic material |
| JPS5981644A (ja) * | 1982-11-01 | 1984-05-11 | Fuji Photo Film Co Ltd | カラ−写真感光材料の処理方法 |
| JPS59188641A (ja) | 1983-04-11 | 1984-10-26 | Fuji Photo Film Co Ltd | ハロゲン化銀写真乳剤 |
| DE3574378D1 (en) * | 1985-09-24 | 1989-12-28 | Eastman Kodak Co | Photographic elements and compositions containing cyclic thioethers |
| US4892803A (en) | 1986-01-23 | 1990-01-09 | Fuji Photo Film Co., Ltd. | Color image-forming process compressing developer containing no benzyl alcohol |
| JPS62239153A (ja) * | 1986-04-11 | 1987-10-20 | Fuji Photo Film Co Ltd | ハロゲン化銀カラ−写真感光材料 |
| AU597408B2 (en) * | 1986-07-10 | 1990-05-31 | Konishiroku Photo Industry Co., Ltd. | Processing silver halide colour photographic materials |
| USH1020H (en) | 1989-09-25 | 1992-02-04 | Konica Corporation | Developing solution for light-sensitive silver halide photographic material and method of forming photographic image making use of it |
| EP0569008B1 (en) * | 1992-05-08 | 1999-02-03 | Eastman Kodak Company | Acceleration of silver removal by thioether compounds |
| US5344750A (en) * | 1992-05-12 | 1994-09-06 | Fuji Photo Film Co., Ltd. | Color development processing method of silver halide color photographic material using a color developer where the color developing agent concentration and processing temperature are a function of bromide ion concentration |
| US5789143A (en) * | 1997-04-30 | 1998-08-04 | Eastman Kodak Company | Thioethers in photographic elements |
| EP2619628B1 (en) | 2010-09-17 | 2014-03-26 | Fujifilm Manufacturing Europe BV | Photographic paper and its use in a photo album |
| GB202006061D0 (en) | 2020-04-24 | 2020-06-10 | Fujifilm Mfg Europe Bv | Photographic paper |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3046129A (en) * | 1958-12-12 | 1962-07-24 | Eastman Kodak Co | Sensitization of photographic silver halide emulsions containing colorforming compounds with polymeric thioethers |
| BE595533A (en, 2012) * | 1959-10-01 | |||
| BE595891A (en, 2012) * | 1959-10-14 |
-
0
- BE BE622218D patent/BE622218A/xx unknown
-
1961
- 1961-09-11 US US137041A patent/US3201242A/en not_active Expired - Lifetime
-
1962
- 1962-09-01 DE DEE23468A patent/DE1147845B/de active Pending
- 1962-09-07 GB GB34357/62A patent/GB1020032A/en not_active Expired
- 1962-09-07 GB GB22017/65A patent/GB1020033A/en not_active Expired
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4254919A (en) * | 1980-05-12 | 1981-03-10 | Polaroid Corporation | Method of loading film cassette |
| US4960683A (en) * | 1987-06-29 | 1990-10-02 | Fuji Photo Film Co., Ltd. | Method for processing a black-and-white photosensitive material |
| EP0704757A1 (en) | 1994-09-29 | 1996-04-03 | Konica Corporation | A silver halide photographic light sensitive material |
| EP0777150A1 (en) | 1995-11-29 | 1997-06-04 | Konica Corporation | Developing composition for silver halide photographic light sensitive material |
Also Published As
| Publication number | Publication date |
|---|---|
| US3201242A (en) | 1965-08-17 |
| GB1020032A (en) | 1966-02-16 |
| GB1020033A (en) | 1966-02-16 |
| BE622218A (en, 2012) |
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