CH493007A - Matériel photographique en feuille, translucide - Google Patents
Matériel photographique en feuille, translucideInfo
- Publication number
- CH493007A CH493007A CH458068A CH458068A CH493007A CH 493007 A CH493007 A CH 493007A CH 458068 A CH458068 A CH 458068A CH 458068 A CH458068 A CH 458068A CH 493007 A CH493007 A CH 493007A
- Authority
- CH
- Switzerland
- Prior art keywords
- sub
- amine
- iodoform
- weight
- chloroform
- Prior art date
Links
- 239000000463 material Substances 0.000 title claims description 23
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 24
- OKJPEAGHQZHRQV-UHFFFAOYSA-N iodoform Chemical compound IC(I)I OKJPEAGHQZHRQV-UHFFFAOYSA-N 0.000 claims description 24
- 239000002243 precursor Substances 0.000 claims description 22
- 150000001412 amines Chemical class 0.000 claims description 21
- 150000001350 alkyl halides Chemical class 0.000 claims description 18
- 229960001701 chloroform Drugs 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 15
- 239000011230 binding agent Substances 0.000 claims description 9
- 238000010438 heat treatment Methods 0.000 claims description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 8
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 8
- 229920006380 polyphenylene oxide Polymers 0.000 claims description 8
- 150000003934 aromatic aldehydes Chemical class 0.000 claims description 7
- -1 phenylbenzylethylamine Iodoform Chemical compound 0.000 claims description 6
- 239000002250 absorbent Substances 0.000 claims description 5
- 230000002745 absorbent Effects 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 5
- 125000004122 cyclic group Chemical group 0.000 claims description 4
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims description 4
- 229920005990 polystyrene resin Polymers 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 4
- QAZLUNIWYYOJPC-UHFFFAOYSA-M sulfenamide Chemical compound [Cl-].COC1=C(C)C=[N+]2C3=NC4=CC=C(OC)C=C4N3SCC2=C1C QAZLUNIWYYOJPC-UHFFFAOYSA-M 0.000 claims description 4
- ZWUBBMDHSZDNTA-UHFFFAOYSA-N 4-Chloro-meta-phenylenediamine Chemical compound NC1=CC=C(Cl)C(N)=C1 ZWUBBMDHSZDNTA-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
- 150000003142 primary aromatic amines Chemical class 0.000 claims description 3
- 229920005989 resin Polymers 0.000 claims description 3
- VDFVNEFVBPFDSB-UHFFFAOYSA-N 1,3-dioxane Chemical compound C1COCOC1 VDFVNEFVBPFDSB-UHFFFAOYSA-N 0.000 claims description 2
- JRBJSXQPQWSCCF-UHFFFAOYSA-N 3,3'-Dimethoxybenzidine Chemical compound C1=C(N)C(OC)=CC(C=2C=C(OC)C(N)=CC=2)=C1 JRBJSXQPQWSCCF-UHFFFAOYSA-N 0.000 claims description 2
- NQHVJMJEWQQXBS-UHFFFAOYSA-N 4-ethoxybenzene-1,3-diamine Chemical compound CCOC1=CC=C(N)C=C1N NQHVJMJEWQQXBS-UHFFFAOYSA-N 0.000 claims description 2
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 claims description 2
- YRCILFLSLZSQHX-UHFFFAOYSA-N S1NCSNC1 Chemical compound S1NCSNC1 YRCILFLSLZSQHX-UHFFFAOYSA-N 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- POJOORKDYOPQLS-UHFFFAOYSA-L barium(2+) 5-chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-methylbenzenesulfonate Chemical compound [Ba+2].C1=C(Cl)C(C)=CC(N=NC=2C3=CC=CC=C3C=CC=2O)=C1S([O-])(=O)=O.C1=C(Cl)C(C)=CC(N=NC=2C3=CC=CC=C3C=CC=2O)=C1S([O-])(=O)=O POJOORKDYOPQLS-UHFFFAOYSA-L 0.000 claims description 2
- 229960001506 brilliant green Drugs 0.000 claims description 2
- 239000000945 filler Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- RUAIJHHRCIHFEV-UHFFFAOYSA-N methyl 4-amino-5-chlorothiophene-2-carboxylate Chemical compound COC(=O)C1=CC(N)=C(Cl)S1 RUAIJHHRCIHFEV-UHFFFAOYSA-N 0.000 claims description 2
- 239000003960 organic solvent Substances 0.000 claims description 2
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229920002522 Wood fibre Polymers 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- NGDLSKPZMOTRTR-OAPYJULQSA-N (4z)-4-heptadecylidene-3-hexadecyloxetan-2-one Chemical compound CCCCCCCCCCCCCCCC\C=C1/OC(=O)C1CCCCCCCCCCCCCCCC NGDLSKPZMOTRTR-OAPYJULQSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical class COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000005840 aryl radicals Chemical class 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 235000003642 hunger Nutrition 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 150000003097 polyterpenes Chemical class 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000011122 softwood Substances 0.000 description 1
- 230000037351 starvation Effects 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000002025 wood fiber 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
- G03C1/675—Compositions containing polyhalogenated compounds as photosensitive substances
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Paper (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US35131664A | 1964-03-12 | 1964-03-12 | |
| US626719A US3394391A (en) | 1967-03-29 | 1967-03-29 | Translucent impregnated paper photographic plate |
| US626881A US3413121A (en) | 1967-03-29 | 1967-03-29 | Heat development of photographic plate containing volatile photosensitizer |
| US626721A US3394394A (en) | 1964-03-12 | 1967-03-29 | Photographic medium based on 5-halofurfurylidenes |
| US641720A US3394395A (en) | 1964-03-12 | 1967-04-21 | Photosensitive medium comprising a furfurylidene, a primary aromatic amine and a lower haloalkane |
| US676637A US3410687A (en) | 1964-03-12 | 1967-10-19 | Photosensitive medium comprising an aromatic protected aldehyde, a primary aromatic amine and a lower haloalkane |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH493007A true CH493007A (fr) | 1970-06-30 |
Family
ID=27559818
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH458068A CH493007A (fr) | 1964-03-12 | 1968-03-28 | Matériel photographique en feuille, translucide |
Country Status (6)
| Country | Link |
|---|---|
| BE (1) | BE712881A (OSRAM) |
| CH (1) | CH493007A (OSRAM) |
| DE (1) | DE1772090C3 (OSRAM) |
| FR (1) | FR1557506A (OSRAM) |
| GB (1) | GB1217899A (OSRAM) |
| NL (1) | NL6804438A (OSRAM) |
-
1968
- 1968-03-27 GB GB1478968A patent/GB1217899A/en not_active Expired
- 1968-03-28 CH CH458068A patent/CH493007A/fr not_active IP Right Cessation
- 1968-03-28 DE DE19681772090 patent/DE1772090C3/de not_active Expired
- 1968-03-28 FR FR1557506D patent/FR1557506A/fr not_active Expired
- 1968-03-28 BE BE712881D patent/BE712881A/xx unknown
- 1968-03-29 NL NL6804438A patent/NL6804438A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| GB1217899A (en) | 1970-12-31 |
| DE1772090B2 (de) | 1973-03-08 |
| FR1557506A (OSRAM) | 1969-02-14 |
| NL6804438A (OSRAM) | 1968-09-30 |
| DE1772090C3 (de) | 1973-09-20 |
| BE712881A (OSRAM) | 1968-09-30 |
| DE1772090A1 (de) | 1971-11-18 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased |