NO130082B - - Google Patents
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- Publication number
- NO130082B NO130082B NO00777/70*[A NO77770A NO130082B NO 130082 B NO130082 B NO 130082B NO 77770 A NO77770 A NO 77770A NO 130082 B NO130082 B NO 130082B
- Authority
- NO
- Norway
- Prior art keywords
- sheet
- heat
- coating
- compound
- acetoacetonitrile
- Prior art date
Links
- 230000005855 radiation Effects 0.000 claims description 19
- 238000000576 coating method Methods 0.000 claims description 13
- 239000011248 coating agent Substances 0.000 claims description 11
- 150000001875 compounds Chemical class 0.000 claims description 11
- 125000003118 aryl group Chemical group 0.000 claims description 7
- -1 caralkyloxy Chemical group 0.000 claims description 7
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 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 claims description 3
- IPBZEJZUAZXNOS-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-oxobutanenitrile Chemical group CC(=O)C(C#N)C1=CC=C(Cl)C=C1 IPBZEJZUAZXNOS-UHFFFAOYSA-N 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 125000000623 heterocyclic group Chemical group 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims 2
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical group CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims 1
- 150000007960 acetonitrile Chemical class 0.000 claims 1
- 150000002825 nitriles Chemical class 0.000 description 11
- 238000001228 spectrum Methods 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 230000009977 dual effect Effects 0.000 description 5
- OPXYNEYEDHAXOM-UHFFFAOYSA-N 3-oxobutanenitrile Chemical class CC(=O)CC#N OPXYNEYEDHAXOM-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- IINNWAYUJNWZRM-UHFFFAOYSA-L erythrosin B Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1C1=C2C=C(I)C(=O)C(I)=C2OC2=C(I)C([O-])=C(I)C=C21 IINNWAYUJNWZRM-UHFFFAOYSA-L 0.000 description 3
- 239000004174 erythrosine Substances 0.000 description 3
- 229940011411 erythrosine Drugs 0.000 description 3
- 235000012732 erythrosine Nutrition 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 125000002587 enol group Chemical group 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 2
- 229910052721 tungsten Inorganic materials 0.000 description 2
- 239000010937 tungsten Substances 0.000 description 2
- ARYNDDWTAHWCPG-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-3-oxobutanenitrile Chemical compound COC1=CC=C(C(C#N)C(C)=O)C=C1OC ARYNDDWTAHWCPG-UHFFFAOYSA-N 0.000 description 1
- MNRQQONRVUGHLY-UHFFFAOYSA-N 2-(3-chlorophenyl)-3-oxobutanenitrile Chemical compound CC(=O)C(C#N)C1=CC=CC(Cl)=C1 MNRQQONRVUGHLY-UHFFFAOYSA-N 0.000 description 1
- KBODHHFICHANMJ-UHFFFAOYSA-N 2-(4-bromophenyl)-3-oxobutanenitrile Chemical compound CC(=O)C(C#N)C1=CC=C(Br)C=C1 KBODHHFICHANMJ-UHFFFAOYSA-N 0.000 description 1
- RCHYZFMBSVFQPT-UHFFFAOYSA-N 2-(4-methoxyphenyl)-3-oxobutanenitrile Chemical compound COC1=CC=C(C(C#N)C(C)=O)C=C1 RCHYZFMBSVFQPT-UHFFFAOYSA-N 0.000 description 1
- QWWANUDFLOXOCB-UHFFFAOYSA-N 2-(4-methylphenyl)-3-oxobutanenitrile Chemical compound CC(=O)C(C#N)C1=CC=C(C)C=C1 QWWANUDFLOXOCB-UHFFFAOYSA-N 0.000 description 1
- OALHHIHQOFIMEF-UHFFFAOYSA-N 3',6'-dihydroxy-2',4',5',7'-tetraiodo-3h-spiro[2-benzofuran-1,9'-xanthene]-3-one Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 OALHHIHQOFIMEF-UHFFFAOYSA-N 0.000 description 1
- RBTBFTRPCNLSDE-UHFFFAOYSA-N 3,7-bis(dimethylamino)phenothiazin-5-ium Chemical compound C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 RBTBFTRPCNLSDE-UHFFFAOYSA-N 0.000 description 1
- KHNWFTMUBKJWRZ-UHFFFAOYSA-N 3-oxo-2-phenylbutanenitrile Chemical compound CC(=O)C(C#N)C1=CC=CC=C1 KHNWFTMUBKJWRZ-UHFFFAOYSA-N 0.000 description 1
- IICCLYANAQEHCI-UHFFFAOYSA-N 4,5,6,7-tetrachloro-3',6'-dihydroxy-2',4',5',7'-tetraiodospiro[2-benzofuran-3,9'-xanthene]-1-one Chemical compound O1C(=O)C(C(=C(Cl)C(Cl)=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 IICCLYANAQEHCI-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 239000011358 absorbing material Substances 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 230000009849 deactivation Effects 0.000 description 1
- SEACYXSIPDVVMV-UHFFFAOYSA-L eosin Y Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C([O-])=C(Br)C=C21 SEACYXSIPDVVMV-UHFFFAOYSA-L 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000002779 inactivation Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229960000907 methylthioninium chloride Drugs 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 229930187593 rose bengal Natural products 0.000 description 1
- 229940081623 rose bengal Drugs 0.000 description 1
- STRXNPAVPKGJQR-UHFFFAOYSA-N rose bengal A Natural products O1C(=O)C(C(=CC=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 STRXNPAVPKGJQR-UHFFFAOYSA-N 0.000 description 1
- OARRHUQTFTUEOS-UHFFFAOYSA-N safranin Chemical compound [Cl-].C=12C=C(N)C(C)=CC2=NC2=CC(C)=C(N)C=C2[N+]=1C1=CC=CC=C1 OARRHUQTFTUEOS-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 229910052720 vanadium Inorganic materials 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
- G03C1/72—Photosensitive compositions not covered by the groups G03C1/005 - G03C1/705
- G03C1/73—Photosensitive compositions not covered by the groups G03C1/005 - G03C1/705 containing organic compounds
-
- 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
- G03C1/494—Silver salt compositions other than silver halide emulsions; Photothermographic systems ; Thermographic systems using noble metal compounds
- G03C1/498—Photothermographic systems, e.g. dry silver
- G03C1/4989—Photothermographic systems, e.g. dry silver characterised by a thermal imaging step, with or without exposure to light, e.g. with a thermal head, using a laser
Landscapes
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US80583969A | 1969-03-10 | 1969-03-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO130082B true NO130082B (xx) | 1974-07-01 |
Family
ID=25192649
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO00777/70*[A NO130082B (xx) | 1969-03-10 | 1970-03-05 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US3619237A (xx) |
| CH (1) | CH511720A (xx) |
| DE (1) | DE2010837A1 (xx) |
| DK (1) | DK122625B (xx) |
| FR (1) | FR2037842A5 (xx) |
| GB (1) | GB1280593A (xx) |
| NL (1) | NL7003340A (xx) |
| NO (1) | NO130082B (xx) |
| SE (1) | SE354730B (xx) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2042054A1 (de) * | 1970-08-25 | 1972-03-02 | Agfa Gevaert Ag | Photographisches Trockenkopierverfahren |
| DE2106577C2 (de) * | 1971-02-11 | 1982-07-08 | Agfa-Gevaert Ag, 5090 Leverkusen | Aufzeichnungsmaterial für das photographische Trockenkopierverfahren und photographisches Verfahren zur Herstellung von Bildern |
| US4291901A (en) * | 1978-11-23 | 1981-09-29 | Ciba-Geigy Corporation | Pressure-sensitive or heat-sensitive recording material |
| US5686228A (en) * | 1996-07-25 | 1997-11-11 | Imation Corp. | Substituted propenitrile compounds as antifoggants for black-and-white photothermographic and thermographic elements |
| CA2452145A1 (en) * | 2003-06-03 | 2004-12-03 | David Tarasenko | Method for producing pulp and lignin |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2680062A (en) * | 1949-07-23 | 1954-06-01 | Keuffel & Esser Co | Process for the production of azo dyestuff images |
| DE1248946B (xx) * | 1959-01-26 | |||
| NL264445A (xx) * | 1959-04-22 | |||
| US3094414A (en) * | 1960-03-15 | 1963-06-18 | Int Nickel Co | Nickel-chromium alloy |
-
1969
- 1969-03-10 US US805839A patent/US3619237A/en not_active Expired - Lifetime
-
1970
- 1970-03-04 SE SE02889/70A patent/SE354730B/xx unknown
- 1970-03-05 NO NO00777/70*[A patent/NO130082B/no unknown
- 1970-03-06 GB GB00760/70A patent/GB1280593A/en not_active Expired
- 1970-03-07 DE DE19702010837 patent/DE2010837A1/de active Pending
- 1970-03-09 FR FR7008395A patent/FR2037842A5/fr not_active Expired
- 1970-03-09 DK DK114470AA patent/DK122625B/da unknown
- 1970-03-09 NL NL7003340A patent/NL7003340A/xx unknown
- 1970-03-09 CH CH343770A patent/CH511720A/fr not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| SE354730B (xx) | 1973-03-19 |
| CH511720A (fr) | 1971-08-31 |
| NL7003340A (xx) | 1970-09-14 |
| GB1280593A (en) | 1972-07-05 |
| US3619237A (en) | 1971-11-09 |
| DK122625B (da) | 1972-03-20 |
| DE2010837A1 (de) | 1970-10-01 |
| FR2037842A5 (xx) | 1970-12-31 |
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