SU525917A1 - Фотографический материал с кислозамещенными и протравными соединени ми - Google Patents
Фотографический материал с кислозамещенными и протравными соединени миInfo
- Publication number
- SU525917A1 SU525917A1 SU1896321A SU1896321A SU525917A1 SU 525917 A1 SU525917 A1 SU 525917A1 SU 1896321 A SU1896321 A SU 1896321A SU 1896321 A SU1896321 A SU 1896321A SU 525917 A1 SU525917 A1 SU 525917A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- dyes
- acidic
- mordant
- compounds
- photographic material
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title claims description 8
- 239000000463 material Substances 0.000 title claims 2
- 230000002378 acidificating effect Effects 0.000 title description 2
- 239000000975 dye Substances 0.000 claims description 14
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 108010010803 Gelatin Proteins 0.000 claims description 4
- 229920000159 gelatin Polymers 0.000 claims description 4
- 239000008273 gelatin Substances 0.000 claims description 4
- 235000019322 gelatine Nutrition 0.000 claims description 4
- 235000011852 gelatine desserts Nutrition 0.000 claims description 4
- 239000000987 azo dye Substances 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 2
- 150000007513 acids Chemical class 0.000 claims description 2
- 150000004985 diamines Chemical class 0.000 claims 1
- 238000009877 rendering Methods 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 239000000243 solution Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 238000005530 etching Methods 0.000 description 3
- 238000005554 pickling Methods 0.000 description 3
- MIVUZIHSIAOKMQ-UHFFFAOYSA-N 1-(diethylamino)-1-(methylamino)henicosan-2-ol Chemical compound C(C)N(C(C(CCCCCCCCCCCCCCCCCCC)O)NC)CC MIVUZIHSIAOKMQ-UHFFFAOYSA-N 0.000 description 2
- VOQTZJYNVJFIJW-UHFFFAOYSA-N 1-amino-3-piperidin-1-ylpropan-2-ol Chemical compound NCC(O)CN1CCCCC1 VOQTZJYNVJFIJW-UHFFFAOYSA-N 0.000 description 2
- KMUWWBNTTNUCDI-UHFFFAOYSA-N 5-amino-1h-imidazo[4,5-d][1,3]oxazin-7-one Chemical class O=C1OC(N)=NC2=C1N=CN2 KMUWWBNTTNUCDI-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- -1 alkyl isocyanate Chemical class 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000000834 fixative Substances 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- 229940090898 Desensitizer Drugs 0.000 description 1
- 241000490229 Eucephalus Species 0.000 description 1
- JXGDJCBMWWDXQX-UHFFFAOYSA-N N-(2-hydroxy-3-piperidin-1-ylpropyl)octadecanamide Chemical compound N1(CCCCC1)CC(CNC(CCCCCCCCCCCCCCCCC)=O)O JXGDJCBMWWDXQX-UHFFFAOYSA-N 0.000 description 1
- PYFSCIWXNSXGNS-UHFFFAOYSA-N N-methylbutan-2-amine Chemical compound CCC(C)NC PYFSCIWXNSXGNS-UHFFFAOYSA-N 0.000 description 1
- 108091007369 NEUR proteins Proteins 0.000 description 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzenecarboxaldehyde Natural products O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 125000005265 dialkylamine group Chemical group 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- SBIDUCNDVPSWQT-UHFFFAOYSA-N n-ethyl-n-(oxiran-2-ylmethyl)ethanamine Chemical compound CCN(CC)CC1CO1 SBIDUCNDVPSWQT-UHFFFAOYSA-N 0.000 description 1
- SZEGKVHRCLBFKJ-UHFFFAOYSA-N n-methyloctadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCNC SZEGKVHRCLBFKJ-UHFFFAOYSA-N 0.000 description 1
- 238000006396 nitration reaction Methods 0.000 description 1
- WTBAHSZERDXKKZ-UHFFFAOYSA-N octadecanoyl chloride Chemical compound CCCCCCCCCCCCCCCCCC(Cl)=O WTBAHSZERDXKKZ-UHFFFAOYSA-N 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000001648 tannin Substances 0.000 description 1
- 229920001864 tannin Polymers 0.000 description 1
- 235000018553 tannin Nutrition 0.000 description 1
- 125000001302 tertiary amino group Chemical group 0.000 description 1
- 239000000080 wetting agent 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
- G03C1/76—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
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Coloring (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DD16363472A DD101032A1 (enrdf_load_html_response) | 1972-06-12 | 1972-06-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU525917A1 true SU525917A1 (ru) | 1976-08-25 |
Family
ID=5486962
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1896321A SU525917A1 (ru) | 1972-06-12 | 1973-03-20 | Фотографический материал с кислозамещенными и протравными соединени ми |
Country Status (10)
| Country | Link |
|---|---|
| AT (1) | AT321103B (enrdf_load_html_response) |
| BE (1) | BE797537A (enrdf_load_html_response) |
| CH (1) | CH575606A5 (enrdf_load_html_response) |
| CS (1) | CS186709B2 (enrdf_load_html_response) |
| DD (1) | DD101032A1 (enrdf_load_html_response) |
| DE (1) | DE2262000A1 (enrdf_load_html_response) |
| FR (1) | FR2188192A1 (enrdf_load_html_response) |
| HU (1) | HU165810B (enrdf_load_html_response) |
| IN (1) | IN141732B (enrdf_load_html_response) |
| SU (1) | SU525917A1 (enrdf_load_html_response) |
-
1972
- 1972-06-12 DD DD16363472A patent/DD101032A1/xx unknown
- 1972-12-19 DE DE19722262000 patent/DE2262000A1/de active Pending
- 1972-12-21 AT AT1091872A patent/AT321103B/de not_active IP Right Cessation
-
1973
- 1973-01-09 CH CH20373A patent/CH575606A5/xx not_active IP Right Cessation
- 1973-03-06 FR FR7307944A patent/FR2188192A1/fr active Granted
- 1973-03-20 SU SU1896321A patent/SU525917A1/ru active
- 1973-03-29 BE BE129447A patent/BE797537A/xx unknown
- 1973-06-07 CS CS413073A patent/CS186709B2/cs unknown
- 1973-06-12 HU HUFI000536 patent/HU165810B/hu unknown
- 1973-11-14 IN IN2502/CAL/73A patent/IN141732B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| FR2188192A1 (en) | 1974-01-18 |
| CS186709B2 (en) | 1978-12-29 |
| HU165810B (enrdf_load_html_response) | 1974-11-28 |
| BE797537A (fr) | 1973-07-16 |
| CH575606A5 (enrdf_load_html_response) | 1976-05-14 |
| IN141732B (enrdf_load_html_response) | 1977-04-09 |
| DE2262000A1 (de) | 1974-01-03 |
| DD101032A1 (enrdf_load_html_response) | 1973-10-12 |
| FR2188192B1 (enrdf_load_html_response) | 1978-08-04 |
| AT321103B (de) | 1975-03-10 |
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