DE2201072A1 - Radiographisches Aufzeichnungsmaterial - Google Patents
Radiographisches AufzeichnungsmaterialInfo
- Publication number
- DE2201072A1 DE2201072A1 DE19722201072 DE2201072A DE2201072A1 DE 2201072 A1 DE2201072 A1 DE 2201072A1 DE 19722201072 DE19722201072 DE 19722201072 DE 2201072 A DE2201072 A DE 2201072A DE 2201072 A1 DE2201072 A1 DE 2201072A1
- Authority
- DE
- Germany
- Prior art keywords
- recording material
- material according
- radiographic recording
- tetrazaindene
- radical
- 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 74
- -1 amino, Hydroxy Chemical group 0.000 claims description 61
- 229910052709 silver Inorganic materials 0.000 claims description 44
- 239000004332 silver Substances 0.000 claims description 44
- 239000000839 emulsion Substances 0.000 claims description 38
- VZYDKJOUEPFKMW-UHFFFAOYSA-N 2,3-dihydroxybenzenesulfonic acid Chemical compound OC1=CC=CC(S(O)(=O)=O)=C1O VZYDKJOUEPFKMW-UHFFFAOYSA-N 0.000 claims description 18
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 17
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 10
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 claims description 8
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 7
- 150000004820 halides Chemical class 0.000 claims description 7
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 6
- 150000002344 gold compounds Chemical class 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 239000011593 sulfur Substances 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 5
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 150000005206 1,2-dihydroxybenzenes Chemical class 0.000 claims description 3
- SRNKZYRMFBGSGE-UHFFFAOYSA-N [1,2,4]triazolo[1,5-a]pyrimidine Chemical compound N1=CC=CN2N=CN=C21 SRNKZYRMFBGSGE-UHFFFAOYSA-N 0.000 claims description 3
- YRACHDVMKITFAZ-UHFFFAOYSA-N [1,2,4]triazolo[4,3-b]pyridazine Chemical compound C1=CC=NN2C=NN=C21 YRACHDVMKITFAZ-UHFFFAOYSA-N 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- TUJKJAMUKRIRHC-UHFFFAOYSA-N hydroxyl Chemical group [OH] TUJKJAMUKRIRHC-UHFFFAOYSA-N 0.000 claims description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N o-dihydroxy-benzene Natural products OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims 1
- 238000000034 method Methods 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 6
- 150000003254 radicals Chemical class 0.000 description 6
- 230000035945 sensitivity Effects 0.000 description 6
- 229910021607 Silver chloride Inorganic materials 0.000 description 5
- 239000000654 additive Substances 0.000 description 5
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 5
- 108010010803 Gelatin Proteins 0.000 description 4
- 229920000159 gelatin Polymers 0.000 description 4
- 239000008273 gelatin Substances 0.000 description 4
- 235000019322 gelatine Nutrition 0.000 description 4
- 235000011852 gelatine desserts Nutrition 0.000 description 4
- 125000001624 naphthyl group Chemical group 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- XXAXVMUWHZHZMJ-UHFFFAOYSA-L 4,5-dihydroxybenzene-1,3-disulfonate Chemical compound OC1=CC(S([O-])(=O)=O)=CC(S([O-])(=O)=O)=C1O XXAXVMUWHZHZMJ-UHFFFAOYSA-L 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- 206010070834 Sensitisation Diseases 0.000 description 3
- 150000003863 ammonium salts Chemical group 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 230000008313 sensitization Effects 0.000 description 3
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 3
- 235000019345 sodium thiosulphate Nutrition 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 229940071240 tetrachloroaurate Drugs 0.000 description 3
- FMCUPJKTGNBGEC-UHFFFAOYSA-N 1,2,4-triazol-4-amine Chemical compound NN1C=NN=C1 FMCUPJKTGNBGEC-UHFFFAOYSA-N 0.000 description 2
- LTPDITOEDOAWRU-UHFFFAOYSA-N 3,4-dihydroxybenzenesulfonic acid Chemical compound OC1=CC=C(S(O)(=O)=O)C=C1O LTPDITOEDOAWRU-UHFFFAOYSA-N 0.000 description 2
- KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical compound NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 description 2
- 239000004133 Sodium thiosulphate Substances 0.000 description 2
- SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 2
- 238000007792 addition Methods 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
- 235000010290 biphenyl Nutrition 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- 125000006267 biphenyl group Chemical group 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- ZUIVNYGZFPOXFW-UHFFFAOYSA-N chembl1717603 Chemical compound N1=C(C)C=C(O)N2N=CN=C21 ZUIVNYGZFPOXFW-UHFFFAOYSA-N 0.000 description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 125000002541 furyl group Chemical group 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000004076 pyridyl group Chemical group 0.000 description 2
- 150000003839 salts Chemical group 0.000 description 2
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 125000003107 substituted aryl group Chemical group 0.000 description 2
- 125000003944 tolyl group Chemical group 0.000 description 2
- APXRHPDHORGIEB-UHFFFAOYSA-N 1H-pyrazolo[4,3-d]pyrimidine Chemical class N1=CN=C2C=NNC2=C1 APXRHPDHORGIEB-UHFFFAOYSA-N 0.000 description 1
- UWZYICUGNHLGSA-UHFFFAOYSA-N 1h-imidazo[4,5-d]pyridazine Chemical class N1=NC=C2NC=NC2=C1 UWZYICUGNHLGSA-UHFFFAOYSA-N 0.000 description 1
- KRTGJZMJJVEKRX-UHFFFAOYSA-N 2-phenylethan-1-yl Chemical compound [CH2]CC1=CC=CC=C1 KRTGJZMJJVEKRX-UHFFFAOYSA-N 0.000 description 1
- NJXWZWXCHBNOOG-UHFFFAOYSA-N 3,3-diphenylpropyl(1-phenylethyl)azanium;chloride Chemical compound [Cl-].C=1C=CC=CC=1C(C)[NH2+]CCC(C=1C=CC=CC=1)C1=CC=CC=C1 NJXWZWXCHBNOOG-UHFFFAOYSA-N 0.000 description 1
- SGYIRNXZLWJMCR-UHFFFAOYSA-M 3-methyl-1,3-benzothiazol-3-ium;iodide Chemical group [I-].C1=CC=C2[N+](C)=CSC2=C1 SGYIRNXZLWJMCR-UHFFFAOYSA-M 0.000 description 1
- KSUYFZWDGGARJN-UHFFFAOYSA-N 4-(5-amino-7-oxo-3h-triazolo[4,5-d]pyrimidin-2-yl)benzoic acid Chemical compound N1=C2C(=O)N=C(N)N=C2NN1C1=CC=C(C(O)=O)C=C1 KSUYFZWDGGARJN-UHFFFAOYSA-N 0.000 description 1
- ZVOYKKFXDAPPRX-UHFFFAOYSA-N 7-chloro-2-(chloromethyl)-5-methyl-[1,2,4]triazolo[1,5-a]pyrimidine Chemical compound N1=C(C)C=C(Cl)N2N=C(CCl)N=C21 ZVOYKKFXDAPPRX-UHFFFAOYSA-N 0.000 description 1
- MGSUQXAMLTWXCB-UHFFFAOYSA-N 7-hydroxy-1h-[1,2,4]triazolo[1,5-a]pyrimidin-5-one Chemical compound OC1=CC(=O)N=C2N=CNN12 MGSUQXAMLTWXCB-UHFFFAOYSA-N 0.000 description 1
- 241001505049 Balantiocheilos melanopterus Species 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- PGIGABCVMQLZOR-UHFFFAOYSA-N C1(=CC=CC=C1)C=1N=C2N=C(C=C(N2N1)O)C Chemical compound C1(=CC=CC=C1)C=1N=C2N=C(C=C(N2N1)O)C PGIGABCVMQLZOR-UHFFFAOYSA-N 0.000 description 1
- BUDVLYURTBUXLE-UHFFFAOYSA-N CCc1c(C)nc2nc(C)nn2c1O Chemical compound CCc1c(C)nc2nc(C)nn2c1O BUDVLYURTBUXLE-UHFFFAOYSA-N 0.000 description 1
- AAJSICXDGLEASV-UHFFFAOYSA-N CCc1c(C)nc2ncnn2c1O Chemical compound CCc1c(C)nc2ncnn2c1O AAJSICXDGLEASV-UHFFFAOYSA-N 0.000 description 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
- YHSNEYLOHWGYMK-UHFFFAOYSA-N N12C(=CC(=NC2=NC=N1)C1CCCCC1)O Chemical compound N12C(=CC(=NC2=NC=N1)C1CCCCC1)O YHSNEYLOHWGYMK-UHFFFAOYSA-N 0.000 description 1
- WCBJYRWGIUTUDN-UHFFFAOYSA-N N1=C(C)C=C(O)N2N=C(C(C)C)N=C21 Chemical compound N1=C(C)C=C(O)N2N=C(C(C)C)N=C21 WCBJYRWGIUTUDN-UHFFFAOYSA-N 0.000 description 1
- LJSPDQNEOIJOKZ-UHFFFAOYSA-N N1=C(C)C=C(O)N2N=C(C)N=C21 Chemical compound N1=C(C)C=C(O)N2N=C(C)N=C21 LJSPDQNEOIJOKZ-UHFFFAOYSA-N 0.000 description 1
- OMFZPUKGAMLFAW-UHFFFAOYSA-N N1=C(C)C=C(O)N2N=C(CCl)N=C21 Chemical compound N1=C(C)C=C(O)N2N=C(CCl)N=C21 OMFZPUKGAMLFAW-UHFFFAOYSA-N 0.000 description 1
- CRHSJHADUMUANM-UHFFFAOYSA-N N1=C(C)C=C(O)N2N=C(CO)N=C21 Chemical compound N1=C(C)C=C(O)N2N=C(CO)N=C21 CRHSJHADUMUANM-UHFFFAOYSA-N 0.000 description 1
- ATSUZWSBVKDCRP-UHFFFAOYSA-N N1=C(C)C=C(O)N2N=C(SC)N=C21 Chemical compound N1=C(C)C=C(O)N2N=C(SC)N=C21 ATSUZWSBVKDCRP-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- DOLWUAMIJZGVTC-UHFFFAOYSA-N [1,2,4]triazolo[4,3-a]pyrimidine Chemical class N1=CC=CN2C=NN=C21 DOLWUAMIJZGVTC-UHFFFAOYSA-N 0.000 description 1
- XEIPQVVAVOUIOP-UHFFFAOYSA-N [Au]=S Chemical compound [Au]=S XEIPQVVAVOUIOP-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 125000004414 alkyl thio group Chemical group 0.000 description 1
- 150000005840 aryl radicals Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- LAABTJXWUKMZIV-UHFFFAOYSA-N benzene-1,4-diol;4-(methylamino)phenol Chemical compound OC1=CC=C(O)C=C1.CNC1=CC=C(O)C=C1 LAABTJXWUKMZIV-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- ZEUDGVUWMXAXEF-UHFFFAOYSA-L bromo(chloro)silver Chemical compound Cl[Ag]Br ZEUDGVUWMXAXEF-UHFFFAOYSA-L 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- ZQRPTUWOEBVAFY-UHFFFAOYSA-N chembl1479966 Chemical compound C1=C(O)N2N=C(C)N=C2N=C1C1=CC=CC=C1 ZQRPTUWOEBVAFY-UHFFFAOYSA-N 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000000068 chlorophenyl group Chemical group 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 150000004683 dihydrates Chemical class 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 1
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229960004251 hydroquinine Drugs 0.000 description 1
- SYLTXFOKMOCILU-UHFFFAOYSA-N imidazo[1,2-b][1,2,4]triazine Chemical class N1=CC=NC2=NC=CN21 SYLTXFOKMOCILU-UHFFFAOYSA-N 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000012224 working solution Substances 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
- G03C1/005—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
- G03C1/08—Sensitivity-increasing substances
- G03C1/09—Noble metals or mercury; Salts or compounds thereof; Sulfur, selenium or tellurium, or compounds thereof, e.g. for chemical sensitising
-
- 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
- G03C1/005—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
- G03C1/08—Sensitivity-increasing substances
- G03C1/10—Organic substances
-
- 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)
- Chemical & Material Sciences (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10563671A | 1971-01-11 | 1971-01-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2201072A1 true DE2201072A1 (de) | 1972-07-27 |
Family
ID=22306953
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19722201072 Pending DE2201072A1 (de) | 1971-01-11 | 1972-01-11 | Radiographisches Aufzeichnungsmaterial |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3671258A (enrdf_load_stackoverflow) |
| BE (1) | BE777887A (enrdf_load_stackoverflow) |
| CA (1) | CA920415A (enrdf_load_stackoverflow) |
| DE (1) | DE2201072A1 (enrdf_load_stackoverflow) |
| FR (1) | FR2121648B1 (enrdf_load_stackoverflow) |
| GB (1) | GB1375101A (enrdf_load_stackoverflow) |
| IT (1) | IT946449B (enrdf_load_stackoverflow) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3891442A (en) * | 1972-12-04 | 1975-06-24 | Eastman Kodak Co | Lithographic materials containing metal complexes |
| JPS5644413B2 (enrdf_load_stackoverflow) * | 1973-05-12 | 1981-10-19 | ||
| US3901712A (en) * | 1974-03-11 | 1975-08-26 | Eastman Kodak Co | Low concentration sensitization and development acceleration |
| US4088494A (en) * | 1974-09-20 | 1978-05-09 | Fuji Photo Film Co., Ltd. | Sulfur-sensitized AgX emulsion containing cubic AgX grains and a mercaptan sensitizer |
| US4078937A (en) * | 1974-11-26 | 1978-03-14 | Fuji Photo Film Co., Ltd. | Process for sensitizing a fine grain silver halide photographic emulsion |
| DE3304330A1 (de) * | 1983-02-09 | 1984-08-09 | Basf Ag, 6700 Ludwigshafen | Neue 2h-v-triazolyl(4,5-d)-pyrimidine und deren verwendung |
| JPH0690476B2 (ja) | 1985-04-25 | 1994-11-14 | コニカ株式会社 | ハロゲン化銀写真感光材料 |
| EP0335107A1 (en) * | 1988-03-01 | 1989-10-04 | EASTMAN KODAK COMPANY (a New Jersey corporation) | Photographic recording material and process for development thereof |
| DE69218876T2 (de) * | 1991-10-24 | 1997-09-25 | Agfa Gevaert Nv | Für Schnellverarbeitungssysteme geeignetes photographisches Silberhalogenidröntgenmaterial |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE530063A (enrdf_load_stackoverflow) * | 1953-07-01 | |||
| FR1365088A (fr) * | 1962-08-04 | 1964-06-26 | Agfa Ag | émulsions photographiques stabilisées contenant des sensibilisateurs d'oxyde de polyalcoylène |
| GB1047492A (enrdf_load_stackoverflow) * | 1963-01-10 | |||
| DE1171266B (de) * | 1963-09-03 | 1964-05-27 | Perutz Photowerke G M B H | Stabilisierung photographischer Emulsionen |
| UST874014I4 (en) * | 1969-12-12 | 1970-05-26 | Defensive publication | |
| US3615535A (en) * | 1970-03-18 | 1971-10-26 | Eastman Kodak Co | Photographic element product composition and process |
-
1971
- 1971-01-11 US US105636A patent/US3671258A/en not_active Expired - Lifetime
- 1971-12-07 CA CA129519A patent/CA920415A/en not_active Expired
-
1972
- 1972-01-06 GB GB60972A patent/GB1375101A/en not_active Expired
- 1972-01-07 FR FR7200399A patent/FR2121648B1/fr not_active Expired
- 1972-01-10 BE BE777887A patent/BE777887A/xx unknown
- 1972-01-11 IT IT19218/72A patent/IT946449B/it active
- 1972-01-11 DE DE19722201072 patent/DE2201072A1/de active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| GB1375101A (enrdf_load_stackoverflow) | 1974-11-27 |
| US3671258A (en) | 1972-06-20 |
| FR2121648A1 (enrdf_load_stackoverflow) | 1972-08-25 |
| CA920415A (en) | 1973-02-06 |
| AU3775072A (en) | 1973-07-12 |
| FR2121648B1 (enrdf_load_stackoverflow) | 1974-04-05 |
| IT946449B (it) | 1973-05-21 |
| BE777887A (fr) | 1972-05-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2422765A1 (de) | Photographische silberhalogenidemulsion | |
| DE69126966T2 (de) | Thiosulfonat-sulfinat-stabilisatoren für photoempfindliche emulsionen | |
| DE2201072A1 (de) | Radiographisches Aufzeichnungsmaterial | |
| DE1278237B (de) | Lichtentwickelbare, direkt kopierende Silberhalogenidemulsion | |
| DE1597462A1 (de) | Fuer Roentgenstrahlen empfindliches photographisches Aufzeichnungsmaterial | |
| DE1177002B (de) | Verfahren zur Verhinderung der Schleierbildung und lichtempfindliche photographische Halogen-silberemulsion bzw. Photomaterial | |
| DE2034064A1 (de) | Lichtempfindliches, gelatinehaltiges farbfotografisches Aufzeichenmatenal | |
| DE2756353C2 (de) | Verfahren zur chemischen Sensibilisierung einer photographischen Silberhalogenidemulsion und photographisches Aufzeichnungsmaterial hiervon | |
| DE2113346A1 (de) | Direktpositivemulsionen mit verbesserter Strahlungsempfindlichkeit | |
| DE2032049C2 (de) | Verfahren zur Entwicklung eines photographischen Aufzeichnungsmaterials | |
| EP0023670B1 (de) | Photographische Emulsion, Verfahren zur Herstellung sowie photographische Materialien | |
| DE2330602A1 (de) | Lichtempfindliches direktpositives silberhalogenidaufzeichnungsmaterial | |
| EP0371359A1 (de) | Verfahren zur Stabilisierung von Silberbildern | |
| DE1106169B (de) | Lichtempfindliches photographisches Material | |
| DE2055103A1 (de) | Sensibihsierung von Silberhalogenid emulsionen | |
| DE2627878C2 (de) | Lichtempfindliches photographisches silberhalogenidhaltiges Aufzeichungsmaterial vom Negativtyp und photographische Entwicklerlösung hierfür | |
| DE1803055C3 (de) | Lichtempfindliches photographisches Aufzeichnungsmaterial | |
| DE2607895A1 (de) | Verfahren zum entwickeln eines lichtempfindlichen photographischen silberhalogenidmaterials | |
| DE69118116T2 (de) | Verbesserte Sensibilisierung von T-Körnern mit einem Nullmethinfarbstoff und einem Tetraazainden | |
| EP0001415A1 (de) | Photographisches Umkehrverfahren mit chemischer Verschleierung, chemische Verschleierungsbäder und ihre Verwendung zur Herstellung photographischer Bilder | |
| DE1547767C (de) | Photographisches Aufzeichnungsmaterial | |
| DE1177003B (de) | Chemisch mit Alkylenoxydkondensaten sensibilisiertes photographisches Material | |
| DE1924534A1 (de) | Photographisches Kopiermaterial mit einem Gehalt eines Antibronzierungsmittels | |
| DE1447569C (de) | Lichtempfindliches photographisches Material | |
| DE1472836C (de) | Chemisch sensibilisierte photographische Silberhalogenidemulsion |