GB1593522A - Vesicular imaging composition material and process - Google Patents
Vesicular imaging composition material and process Download PDFInfo
- Publication number
- GB1593522A GB1593522A GB46260/77A GB4626077A GB1593522A GB 1593522 A GB1593522 A GB 1593522A GB 46260/77 A GB46260/77 A GB 46260/77A GB 4626077 A GB4626077 A GB 4626077A GB 1593522 A GB1593522 A GB 1593522A
- Authority
- GB
- United Kingdom
- Prior art keywords
- composition
- cyclopropenone
- binder
- vesiculating
- polymer
- 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.)
- Expired
Links
- 238000003384 imaging method Methods 0.000 title claims description 24
- 238000000034 method Methods 0.000 title claims description 22
- 230000008569 process Effects 0.000 title claims description 11
- 239000002131 composite material Substances 0.000 title 1
- 239000000463 material Substances 0.000 claims description 65
- GGRQLKPIJPFWEZ-UHFFFAOYSA-N cycloprop-2-en-1-one Chemical compound O=C1C=C1 GGRQLKPIJPFWEZ-UHFFFAOYSA-N 0.000 claims description 54
- 239000003795 chemical substances by application Substances 0.000 claims description 50
- 239000011230 binding agent Substances 0.000 claims description 48
- -1 alkoxy radical Chemical class 0.000 claims description 43
- 239000000203 mixture Substances 0.000 claims description 41
- 230000003595 spectral effect Effects 0.000 claims description 38
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 36
- 229920000642 polymer Polymers 0.000 claims description 29
- 230000035945 sensitivity Effects 0.000 claims description 16
- 125000004432 carbon atom Chemical group C* 0.000 claims description 15
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 13
- 239000005977 Ethylene Substances 0.000 claims description 13
- 238000010438 heat treatment Methods 0.000 claims description 13
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- HCIBTBXNLVOFER-UHFFFAOYSA-N diphenylcyclopropenone Chemical group O=C1C(C=2C=CC=CC=2)=C1C1=CC=CC=C1 HCIBTBXNLVOFER-UHFFFAOYSA-N 0.000 claims description 5
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- IXXVQSMMCWOKNU-UHFFFAOYSA-N 2-[(5e)-5-(3-ethyl-2h-1,3-benzothiazol-1-ylidene)-4-oxo-2-sulfanylidene-1,3-thiazolidin-3-yl]acetic acid Chemical compound C12=CC=CC=C2N(CC)C\S1=C1\SC(=S)N(CC(O)=O)C1=O IXXVQSMMCWOKNU-UHFFFAOYSA-N 0.000 claims description 3
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- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
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- 238000001914 filtration Methods 0.000 description 3
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
- 229910052753 mercury Inorganic materials 0.000 description 3
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- 238000002360 preparation method Methods 0.000 description 3
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- BLZOHTXDDOAASQ-UHFFFAOYSA-N 1,2,3,3-tetrachlorocyclopropene Chemical compound ClC1=C(Cl)C1(Cl)Cl BLZOHTXDDOAASQ-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
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- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 238000000149 argon plasma sintering Methods 0.000 description 2
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- 125000000623 heterocyclic group Chemical group 0.000 description 2
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- 230000031700 light absorption Effects 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
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- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 239000006069 physical mixture Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229910052711 selenium Chemical group 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000000565 sulfonamide group Chemical group 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000001429 visible spectrum Methods 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 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
- G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
- G03C5/60—Processes for obtaining vesicular images
-
- 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
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/739,774 US4128422A (en) | 1976-11-08 | 1976-11-08 | Cyclopropenone vesicular imaging composition, element and process |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1593522A true GB1593522A (en) | 1981-07-15 |
Family
ID=24973734
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB46260/77A Expired GB1593522A (en) | 1976-11-08 | 1977-11-07 | Vesicular imaging composition material and process |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US4128422A (enExample) |
| CA (1) | CA1078659A (enExample) |
| FR (1) | FR2370304A1 (enExample) |
| GB (1) | GB1593522A (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6794107B2 (en) | 2002-10-28 | 2004-09-21 | Kodak Polychrome Graphics Llc | Thermal generation of a mask for flexography |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2965081D1 (en) * | 1978-12-11 | 1983-04-28 | Bexford Ltd | Vesicular recording materials and process for their production |
| US4368247A (en) * | 1981-06-29 | 1983-01-11 | Eastman Kodak Company | Photographic materials and processes comprising oxoindolizine and oxoindolizinium compounds |
| US4450093A (en) * | 1981-06-29 | 1984-05-22 | Eastman Kodak Company | Indolizinone dyes and compositions, elements and methods using same |
| US4373021A (en) * | 1981-06-29 | 1983-02-08 | Eastman Kodak Company | Indolizinone dyes and compositions, elements and methods using same |
| US4577024A (en) * | 1981-06-29 | 1986-03-18 | Eastman Kodak Company | Oxoindolizine and oxoindolizinium compounds useful as dyes |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1952787A (en) * | 1930-06-09 | 1934-03-27 | Photo Cast Inc | Method of printing |
| US3091532A (en) * | 1960-12-30 | 1963-05-28 | Ibm | Vesicular image photography process with polyketone photographic films |
| US3355295A (en) * | 1964-02-11 | 1967-11-28 | Eastman Kodak Co | Nucleated vesicular film |
| US3657348A (en) * | 1968-05-03 | 1972-04-18 | Dow Chemical Co | Disubstituted cyclopropenones and method of production |
| DE2121014A1 (de) * | 1971-04-29 | 1972-11-02 | Agfa-Gevaert Ag, 5090 Leverkusen | Sensibilisierte elektrophotographische Schichten |
-
1976
- 1976-11-08 US US05/739,774 patent/US4128422A/en not_active Expired - Lifetime
-
1977
- 1977-02-01 CA CA270,840A patent/CA1078659A/en not_active Expired
- 1977-11-07 GB GB46260/77A patent/GB1593522A/en not_active Expired
- 1977-11-08 FR FR7733517A patent/FR2370304A1/fr active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6794107B2 (en) | 2002-10-28 | 2004-09-21 | Kodak Polychrome Graphics Llc | Thermal generation of a mask for flexography |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2370304A1 (fr) | 1978-06-02 |
| FR2370304B1 (enExample) | 1981-01-02 |
| CA1078659A (en) | 1980-06-03 |
| US4128422A (en) | 1978-12-05 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| CSNS | Application of which complete specification have been accepted and published, but patent is not sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |