DE2010822A1 - Kopierpapier - Google Patents
KopierpapierInfo
- Publication number
- DE2010822A1 DE2010822A1 DE19702010822 DE2010822A DE2010822A1 DE 2010822 A1 DE2010822 A1 DE 2010822A1 DE 19702010822 DE19702010822 DE 19702010822 DE 2010822 A DE2010822 A DE 2010822A DE 2010822 A1 DE2010822 A1 DE 2010822A1
- Authority
- DE
- Germany
- Prior art keywords
- sheet
- pyrazolone
- pyrazolin
- color
- methyl
- 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
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 claims description 22
- 230000005855 radiation Effects 0.000 claims description 18
- 239000001856 Ethyl cellulose Substances 0.000 claims description 4
- 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 claims description 4
- 239000011230 binding agent Substances 0.000 claims description 4
- 229920001249 ethyl cellulose Polymers 0.000 claims description 4
- 235000019325 ethyl cellulose Nutrition 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 4
- 239000000463 material Substances 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 description 8
- -1 1,3 diphenyl-2-pyrazolin-5-one 3,4-dimethyl-1-phenyl-2-pyrazolin-5-one Chemical compound 0.000 description 6
- 238000001228 spectrum Methods 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 4
- 229940051880 analgesics and antipyretics pyrazolones Drugs 0.000 description 3
- VEQOALNAAJBPNY-UHFFFAOYSA-N antipyrine Chemical compound CN1C(C)=CC(=O)N1C1=CC=CC=C1 VEQOALNAAJBPNY-UHFFFAOYSA-N 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 150000001989 diazonium salts Chemical class 0.000 description 3
- 150000002431 hydrogen Chemical class 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- IOQOLGUXWSBWHR-UHFFFAOYSA-N 5-methyl-2-(4-methylphenyl)-4h-pyrazol-3-one Chemical compound O=C1CC(C)=NN1C1=CC=C(C)C=C1 IOQOLGUXWSBWHR-UHFFFAOYSA-N 0.000 description 2
- RLFWWDJHLFCNIJ-UHFFFAOYSA-N Aminoantipyrine Natural products CN1C(C)=C(N)C(=O)N1C1=CC=CC=C1 RLFWWDJHLFCNIJ-UHFFFAOYSA-N 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 239000012954 diazonium Substances 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-O diazynium Chemical class [NH+]#N IJGRMHOSHXDMSA-UHFFFAOYSA-O 0.000 description 2
- 230000009977 dual effect Effects 0.000 description 2
- 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 2
- 239000004174 erythrosine Substances 0.000 description 2
- 229940011411 erythrosine Drugs 0.000 description 2
- 235000012732 erythrosine Nutrition 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 229960005222 phenazone Drugs 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 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
- DDWXNUFFAFBJDG-UHFFFAOYSA-N 1-acetyl-2-sulfanylideneimidazolidin-4-one Chemical compound CC(=O)N1CC(=O)NC1=S DDWXNUFFAFBJDG-UHFFFAOYSA-N 0.000 description 1
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 1
- RIOMUJXIGYZENC-UHFFFAOYSA-N 2-(3-chlorophenyl)-5-methyl-4h-pyrazol-3-one Chemical compound O=C1CC(C)=NN1C1=CC=CC(Cl)=C1 RIOMUJXIGYZENC-UHFFFAOYSA-N 0.000 description 1
- GLGRRRKQSFURGD-UHFFFAOYSA-N 2-phenyl-5-(trifluoromethyl)-4h-pyrazol-3-one Chemical compound O=C1CC(C(F)(F)F)=NN1C1=CC=CC=C1 GLGRRRKQSFURGD-UHFFFAOYSA-N 0.000 description 1
- OXRSFHYBIRFJSF-UHFFFAOYSA-N 3-phenyl-1,4-dihydropyrazol-5-one Chemical compound N1C(=O)CC(C=2C=CC=CC=2)=N1 OXRSFHYBIRFJSF-UHFFFAOYSA-N 0.000 description 1
- LPOVZHYARSAVIZ-UHFFFAOYSA-N 5-amino-2-phenyl-4h-pyrazol-3-one Chemical compound O=C1CC(N)=NN1C1=CC=CC=C1 LPOVZHYARSAVIZ-UHFFFAOYSA-N 0.000 description 1
- MRQNFRMHWBTRGX-UHFFFAOYSA-N 5-methyl-2-(2,4,6-trichlorophenyl)-4h-pyrazol-3-one Chemical compound O=C1CC(C)=NN1C1=C(Cl)C=C(Cl)C=C1Cl MRQNFRMHWBTRGX-UHFFFAOYSA-N 0.000 description 1
- GENSTRUCMIZOCD-UHFFFAOYSA-N 5-methyl-2-(2-methylphenyl)-4h-pyrazol-3-one Chemical compound O=C1CC(C)=NN1C1=CC=CC=C1C GENSTRUCMIZOCD-UHFFFAOYSA-N 0.000 description 1
- BNILDNQGLCOHLV-UHFFFAOYSA-N 5-methyl-2-(3-nitrophenyl)-4h-pyrazol-3-one Chemical compound O=C1CC(C)=NN1C1=CC=CC([N+]([O-])=O)=C1 BNILDNQGLCOHLV-UHFFFAOYSA-N 0.000 description 1
- RMMXTBMQSGEXHJ-UHFFFAOYSA-N Aminophenazone Chemical compound O=C1C(N(C)C)=C(C)N(C)N1C1=CC=CC=C1 RMMXTBMQSGEXHJ-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 229960000212 aminophenazone Drugs 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- UKJLNMAFNRKWGR-UHFFFAOYSA-N cyclohexatrienamine Chemical group NC1=CC=C=C[CH]1 UKJLNMAFNRKWGR-UHFFFAOYSA-N 0.000 description 1
- 238000000586 desensitisation Methods 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- QELUYTUMUWHWMC-UHFFFAOYSA-N edaravone Chemical compound O=C1CC(C)=NN1C1=CC=CC=C1 QELUYTUMUWHWMC-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- NJSUFZNXBBXAAC-UHFFFAOYSA-N ethanol;toluene Chemical compound CCO.CC1=CC=CC=C1 NJSUFZNXBBXAAC-UHFFFAOYSA-N 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000002779 inactivation Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- CMCWWLVWPDLCRM-UHFFFAOYSA-N phenidone Chemical compound N1C(=O)CCN1C1=CC=CC=C1 CMCWWLVWPDLCRM-UHFFFAOYSA-N 0.000 description 1
- NDGRWYRVNANFNB-UHFFFAOYSA-N pyrazolidin-3-one Chemical compound O=C1CCNN1 NDGRWYRVNANFNB-UHFFFAOYSA-N 0.000 description 1
- 150000003219 pyrazolines Chemical class 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000004043 responsiveness Effects 0.000 description 1
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 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 |
|---|---|---|---|
| US80584069A | 1969-03-10 | 1969-03-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2010822A1 true DE2010822A1 (de) | 1970-10-01 |
Family
ID=25192654
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19702010822 Pending DE2010822A1 (de) | 1969-03-10 | 1970-03-07 | Kopierpapier |
Country Status (7)
| Country | Link |
|---|---|
| CH (1) | CH511721A (enrdf_load_stackoverflow) |
| DE (1) | DE2010822A1 (enrdf_load_stackoverflow) |
| DK (1) | DK122626B (enrdf_load_stackoverflow) |
| FR (1) | FR2037847A5 (enrdf_load_stackoverflow) |
| GB (1) | GB1296969A (enrdf_load_stackoverflow) |
| NL (1) | NL7003339A (enrdf_load_stackoverflow) |
| SE (1) | SE354731B (enrdf_load_stackoverflow) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5637550A (en) * | 1995-03-02 | 1997-06-10 | Agfa-Gevaert N.V. | Heat-sensitive recording material having image-stabilization properties |
| EP0730196A3 (en) * | 1995-03-02 | 1998-01-21 | Agfa-Gevaert N.V. | Heat-sensitive recording material having image-stabilization properties |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5821251B2 (ja) * | 1978-08-28 | 1983-04-28 | 旭化成株式会社 | 乾式画像形成材料 |
-
1970
- 1970-03-04 SE SE289070A patent/SE354731B/xx unknown
- 1970-03-06 GB GB1296969D patent/GB1296969A/en not_active Expired
- 1970-03-07 DE DE19702010822 patent/DE2010822A1/de active Pending
- 1970-03-09 DK DK114570A patent/DK122626B/da unknown
- 1970-03-09 NL NL7003339A patent/NL7003339A/xx unknown
- 1970-03-09 CH CH343870A patent/CH511721A/fr not_active IP Right Cessation
- 1970-03-09 FR FR7008402A patent/FR2037847A5/fr not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5637550A (en) * | 1995-03-02 | 1997-06-10 | Agfa-Gevaert N.V. | Heat-sensitive recording material having image-stabilization properties |
| EP0730196A3 (en) * | 1995-03-02 | 1998-01-21 | Agfa-Gevaert N.V. | Heat-sensitive recording material having image-stabilization properties |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2037847A5 (enrdf_load_stackoverflow) | 1970-12-31 |
| DK122626B (da) | 1972-03-20 |
| SE354731B (enrdf_load_stackoverflow) | 1973-03-19 |
| CH511721A (fr) | 1971-08-31 |
| NL7003339A (enrdf_load_stackoverflow) | 1970-09-14 |
| GB1296969A (enrdf_load_stackoverflow) | 1972-11-22 |
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