RU2009141370A - РАДИАЦИОННО-СШИВАЕМЫЕ И ТЕРМИЧЕСКИ-СШИВАЕМЫЕ ПОЛИУРЕТАНОВЫЕ СИСТЕМЫ НА ОСНОВЕ ПОЛИ(ε-КАПРОЛАКТОН)ПОЛИСЛОЖНОЭФИРНЫХ ПОЛИОЛОВ - Google Patents
РАДИАЦИОННО-СШИВАЕМЫЕ И ТЕРМИЧЕСКИ-СШИВАЕМЫЕ ПОЛИУРЕТАНОВЫЕ СИСТЕМЫ НА ОСНОВЕ ПОЛИ(ε-КАПРОЛАКТОН)ПОЛИСЛОЖНОЭФИРНЫХ ПОЛИОЛОВ Download PDFInfo
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- RU2009141370A RU2009141370A RU2009141370/04A RU2009141370A RU2009141370A RU 2009141370 A RU2009141370 A RU 2009141370A RU 2009141370/04 A RU2009141370/04 A RU 2009141370/04A RU 2009141370 A RU2009141370 A RU 2009141370A RU 2009141370 A RU2009141370 A RU 2009141370A
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- Prior art keywords
- polyurethane compositions
- compositions according
- poly
- caprolactone
- polyols
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- 239000004814 polyurethane Substances 0.000 title claims abstract 16
- 229920002635 polyurethane Polymers 0.000 title claims abstract 16
- 229920005862 polyol Polymers 0.000 title claims abstract 8
- 229920001610 polycaprolactone Polymers 0.000 title claims abstract 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 title 1
- 239000000203 mixture Substances 0.000 claims abstract 15
- 150000001875 compounds Chemical class 0.000 claims abstract 8
- 229920003023 plastic Polymers 0.000 claims abstract 8
- 239000004033 plastic Substances 0.000 claims abstract 8
- 229920000642 polymer Polymers 0.000 claims abstract 7
- -1 naphthyl acrylate Chemical compound 0.000 claims abstract 4
- 229920001228 polyisocyanate Polymers 0.000 claims abstract 4
- 239000005056 polyisocyanate Substances 0.000 claims abstract 4
- 150000003077 polyols Chemical class 0.000 claims abstract 4
- BKKVYNMMVYEBGR-UHFFFAOYSA-N (2,3,4,5,6-pentabromophenyl) prop-2-enoate Chemical compound BrC1=C(Br)C(Br)=C(OC(=O)C=C)C(Br)=C1Br BKKVYNMMVYEBGR-UHFFFAOYSA-N 0.000 claims abstract 2
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 claims abstract 2
- VSVDQVJQWXJJSS-UHFFFAOYSA-N [2,6-dibromo-4-[2-(3,5-dibromo-4-prop-2-enoyloxyphenyl)propan-2-yl]phenyl] prop-2-enoate Chemical compound C=1C(Br)=C(OC(=O)C=C)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(OC(=O)C=C)C(Br)=C1 VSVDQVJQWXJJSS-UHFFFAOYSA-N 0.000 claims abstract 2
- FHLPGTXWCFQMIU-UHFFFAOYSA-N [4-[2-(4-prop-2-enoyloxyphenyl)propan-2-yl]phenyl] prop-2-enoate Chemical compound C=1C=C(OC(=O)C=C)C=CC=1C(C)(C)C1=CC=C(OC(=O)C=C)C=C1 FHLPGTXWCFQMIU-UHFFFAOYSA-N 0.000 claims abstract 2
- 125000001931 aliphatic group Chemical group 0.000 claims abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract 2
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 claims abstract 2
- 238000006116 polymerization reaction Methods 0.000 claims abstract 2
- 150000003254 radicals Chemical class 0.000 claims abstract 2
- 239000003381 stabilizer Substances 0.000 claims abstract 2
- BNVGSJJCBGOPRP-UHFFFAOYSA-N C(C=C)(=O)OCC(CC(COC1=C(C=C(C=C1Br)C(C)(C)C1=CC(=C(C(=C1)Br)OCC(CC(COC(C=C)=O)O)OC(CC(C1=CC=C(C=C1)Cl)(C1=CC=C(C=C1)Cl)C1=CC=C(C=C1)Cl)=O)Br)Br)OC(CC(C1=CC=C(C=C1)Cl)(C1=CC=C(C=C1)Cl)C1=CC=C(C=C1)Cl)=O)O Chemical compound C(C=C)(=O)OCC(CC(COC1=C(C=C(C=C1Br)C(C)(C)C1=CC(=C(C(=C1)Br)OCC(CC(COC(C=C)=O)O)OC(CC(C1=CC=C(C=C1)Cl)(C1=CC=C(C=C1)Cl)C1=CC=C(C=C1)Cl)=O)Br)Br)OC(CC(C1=CC=C(C=C1)Cl)(C1=CC=C(C=C1)Cl)C1=CC=C(C=C1)Cl)=O)O BNVGSJJCBGOPRP-UHFFFAOYSA-N 0.000 claims 1
- 230000009477 glass transition Effects 0.000 claims 1
- 238000000465 moulding Methods 0.000 claims 1
- 229920000728 polyester Polymers 0.000 claims 1
- 229920005906 polyester polyol Polymers 0.000 abstract 3
- CQJHZEKRPXIFFR-UHFFFAOYSA-N [1-[2,6-dibromo-4-[2-[3,5-dibromo-4-[3-(2-prop-2-enoyloxyethoxy)-2-[3,3,3-tris(4-chlorophenyl)propanoyloxy]propoxy]phenyl]propan-2-yl]phenoxy]-3-(2-prop-2-enoyloxyethoxy)propan-2-yl] 3,3,3-tris(4-chlorophenyl)propanoate Chemical compound C=1C(Br)=C(OCC(COCCOC(=O)C=C)OC(=O)CC(C=2C=CC(Cl)=CC=2)(C=2C=CC(Cl)=CC=2)C=2C=CC(Cl)=CC=2)C(Br)=CC=1C(C)(C)C(C=C1Br)=CC(Br)=C1OCC(COCCOC(=O)C=C)OC(=O)CC(C=1C=CC(Cl)=CC=1)(C=1C=CC(Cl)=CC=1)C1=CC=C(Cl)C=C1 CQJHZEKRPXIFFR-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/63—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers
- C08G18/631—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers onto polyesters and/or polycarbonates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/4266—Polycondensates having carboxylic or carbonic ester groups in the main chain prepared from hydroxycarboxylic acids and/or lactones
- C08G18/4269—Lactones
- C08G18/4277—Caprolactone and/or substituted caprolactone
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/63—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers
- C08G18/638—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers characterised by the use of compounds having carbon-to-carbon double bonds other than styrene and/or olefinic nitriles
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
- C08G18/78—Nitrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
- C08G18/78—Nitrogen
- C08G18/7875—Nitrogen containing heterocyclic rings having at least one nitrogen atom in the ring
- C08G18/7887—Nitrogen containing heterocyclic rings having at least one nitrogen atom in the ring having two nitrogen atoms in the ring
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
- C08G18/78—Nitrogen
- C08G18/79—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
- C08G18/798—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing urethdione groups
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03H—HOLOGRAPHIC PROCESSES OR APPARATUS
- G03H1/00—Holographic processes or apparatus using light, infrared or ultraviolet waves for obtaining holograms or for obtaining an image from them; Details peculiar thereto
- G03H1/02—Details of features involved during the holographic process; Replication of holograms without interference recording
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/241—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
- G11B7/242—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers
- G11B7/244—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only
- G11B7/245—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing a polymeric component
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03H—HOLOGRAPHIC PROCESSES OR APPARATUS
- G03H1/00—Holographic processes or apparatus using light, infrared or ultraviolet waves for obtaining holograms or for obtaining an image from them; Details peculiar thereto
- G03H1/02—Details of features involved during the holographic process; Replication of holograms without interference recording
- G03H2001/026—Recording materials or recording processes
- G03H2001/0264—Organic recording material
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/2403—Layers; Shape, structure or physical properties thereof
- G11B7/24035—Recording layers
- G11B7/24044—Recording layers for storing optical interference patterns, e.g. holograms; for storing data in three dimensions, e.g. volume storage
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- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Polyurethanes Or Polyureas (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
1. Полиуретановые композиции, содержащие ! A) один или более полиизоцианатов, ! B) один или более полиолов, содержащих, по меньшей мере, один поли(ε-капролактон)поли-сложноэфирный полиол, ! C) одно или более соединений, имеющих группы, которые при актиничном облучении реагируют с соединениями, ненасыщенными по этиленовому типу (радиационно-отверждаемые соединения), с полимеризацией, ! D) необязательно один или более свободнорадикальных стабилизаторов и ! E) один или более фотоинициаторов. !2. Полиуретановые композиции по п.1, в которых, по меньшей мере, 60 мас.% полиизоцианатов компонента A) основано на алифатических и/или циклоалифатических ди- и/или триизоцианатах. ! 3. Полиуретановые композиции по п.1, в которых доля поли(ε-капролактон)поли-сложноэфирных полиолов, из расчета на полиолы компонента B), составляет, по меньшей мере, 20 мас.%. ! 4. Полиуретановые композиции по п.1, в которых поли(ε-капролактон)поли-сложноэфирные полиолы компонента В) имеют среднечисловые молярные массы от 500 до 2000 г/моль и среднюю OH функциональность от 1.5 до 4. ! 5. Полиуретановые композиции по п.1, в которых молярное соотношение NCO и OH групп составляет от 0.95 до 1.25. ! 6. Полиуретановые композиции по п.1, в которых одно или более соединений из группы, состоящей из 9-винилкарбазола, винилнафталина, диакрилата бисфенола A, диакрилата тетрабромбисфенола A, 1,4-бис(2-тионафтил)-2-бутилакрилата, пентабромфенилакрилата, нафтилакрилата и пропан-2,2-диилбис[(2,6-дибром-4,1-фенилен)окси(2-{[3,3,3-трис(4-хлорфенил)пропаноил]окси}пропан-3,1-диил)оксиэтан-2,1-диил]диакрилата, применяется в C). ! 7. Полимерные пластмассы, полученные из полиуретановых композиций по п.1. ! 8. Полимерные пластм�
Claims (11)
1. Полиуретановые композиции, содержащие
A) один или более полиизоцианатов,
B) один или более полиолов, содержащих, по меньшей мере, один поли(ε-капролактон)поли-сложноэфирный полиол,
C) одно или более соединений, имеющих группы, которые при актиничном облучении реагируют с соединениями, ненасыщенными по этиленовому типу (радиационно-отверждаемые соединения), с полимеризацией,
D) необязательно один или более свободнорадикальных стабилизаторов и
E) один или более фотоинициаторов.
2. Полиуретановые композиции по п.1, в которых, по меньшей мере, 60 мас.% полиизоцианатов компонента A) основано на алифатических и/или циклоалифатических ди- и/или триизоцианатах.
3. Полиуретановые композиции по п.1, в которых доля поли(ε-капролактон)поли-сложноэфирных полиолов, из расчета на полиолы компонента B), составляет, по меньшей мере, 20 мас.%.
4. Полиуретановые композиции по п.1, в которых поли(ε-капролактон)поли-сложноэфирные полиолы компонента В) имеют среднечисловые молярные массы от 500 до 2000 г/моль и среднюю OH функциональность от 1.5 до 4.
5. Полиуретановые композиции по п.1, в которых молярное соотношение NCO и OH групп составляет от 0.95 до 1.25.
6. Полиуретановые композиции по п.1, в которых одно или более соединений из группы, состоящей из 9-винилкарбазола, винилнафталина, диакрилата бисфенола A, диакрилата тетрабромбисфенола A, 1,4-бис(2-тионафтил)-2-бутилакрилата, пентабромфенилакрилата, нафтилакрилата и пропан-2,2-диилбис[(2,6-дибром-4,1-фенилен)окси(2-{[3,3,3-трис(4-хлорфенил)пропаноил]окси}пропан-3,1-диил)оксиэтан-2,1-диил]диакрилата, применяется в C).
7. Полимерные пластмассы, полученные из полиуретановых композиций по п.1.
8. Полимерные пластмассы по п.7, где полимерные пластмассы представляют собой слои или литье.
9. Полимерные пластмассы по п.7, где полимерные пластмассы имеют температуру стеклования ниже -40°C.
10. Голографические среды, содержащие полиуретановые композиции по п.1.
11. Голографические среды, содержащие, по меньшей мере, одну полимерную пластмассу по любому из пп.7-9.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US92298107P | 2007-04-11 | 2007-04-11 | |
| US60/922,981 | 2007-04-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| RU2009141370A true RU2009141370A (ru) | 2011-05-20 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
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| RU2009141370/04A RU2009141370A (ru) | 2007-04-11 | 2008-03-28 | РАДИАЦИОННО-СШИВАЕМЫЕ И ТЕРМИЧЕСКИ-СШИВАЕМЫЕ ПОЛИУРЕТАНОВЫЕ СИСТЕМЫ НА ОСНОВЕ ПОЛИ(ε-КАПРОЛАКТОН)ПОЛИСЛОЖНОЭФИРНЫХ ПОЛИОЛОВ |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US20080311483A1 (ru) |
| EP (1) | EP2144946A1 (ru) |
| JP (1) | JP2010523776A (ru) |
| KR (1) | KR20100015472A (ru) |
| CN (1) | CN101657483A (ru) |
| BR (1) | BRPI0809620A2 (ru) |
| CA (1) | CA2683902A1 (ru) |
| IL (1) | IL201036A0 (ru) |
| RU (1) | RU2009141370A (ru) |
| TW (1) | TW200906882A (ru) |
| WO (1) | WO2008125202A1 (ru) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BRPI0810155A2 (pt) * | 2007-04-11 | 2014-12-30 | Bayer Materialscience Ag | Meios de gravação para aplicações holográficas. |
| WO2008125200A1 (en) * | 2007-04-11 | 2008-10-23 | Bayer Materialscience Ag | Radiation-crosslinking and thermally crosslinking pu systems based on isocyanate-reactive block copolymers |
| CA2683901A1 (en) * | 2007-04-11 | 2008-10-23 | Bayer Materialscience Ag | Radiation-crosslinking and thermally crosslinking pu systems comprising iminooxadiazinedione |
| IL200996A0 (en) * | 2008-10-01 | 2010-06-30 | Bayer Materialscience Ag | Photopolymer formulations having a low crosslinking density |
| WO2010037515A1 (de) * | 2008-10-01 | 2010-04-08 | Bayer Materialscience Ag | Medien für volumenholographische aufzeichnung basierend auf sich selbstentwickelndem polymer |
| EP2218743A1 (de) * | 2009-02-12 | 2010-08-18 | Bayer MaterialScience AG | Prepolymerbasierte Polyurethanformulierungen zur Herstellung holographischer Filme |
| US8284234B2 (en) | 2009-03-20 | 2012-10-09 | Absolute Imaging LLC | Endoscopic imaging using reflection holographic optical element for autostereoscopic 3-D viewing |
| EP2316866A1 (de) * | 2009-10-29 | 2011-05-04 | Bayer MaterialScience AG | Wässrige Zubereitung auf Basis kristalliner oder semikristalliner Polyurethanpolymere |
| JP2013510203A (ja) * | 2009-11-03 | 2013-03-21 | バイエル・マテリアルサイエンス・アクチェンゲゼルシャフト | 感光性ポリマー組成物における添加剤としてのフルオロウレタン |
| US8771904B2 (en) * | 2009-11-03 | 2014-07-08 | Bayer Materialscience Ag | Method for producing holographic media |
| EP2497085B1 (de) * | 2009-11-03 | 2014-02-12 | Bayer Intellectual Property GmbH | Verfahren zur herstellung eines holographischen films |
| ES2535950T3 (es) | 2009-11-03 | 2015-05-19 | Bayer Intellectual Property Gmbh | Uretanos como aditivos en una formulación de fotopolímeros |
| BR112016029755A2 (pt) * | 2014-06-23 | 2017-08-22 | Carbon Inc | métodos de produção de objetos tridimensionais a partir de materiais tendo múltiplos mecanismos de endurecimento |
| EP3396455B1 (de) | 2017-04-28 | 2022-10-05 | Technische Universität Wien | Lichthärtbare zusammensetzung |
| KR102654431B1 (ko) * | 2018-08-09 | 2024-04-03 | 미쯔비시 케미컬 주식회사 | 홀로그램 기록 매체용 조성물 및 홀로그램 기록 매체 |
| EP3838592A1 (en) * | 2019-12-17 | 2021-06-23 | Evonik Operations GmbH | Composition comprising polyesters for additive manufacturing |
| CN116284650A (zh) * | 2023-04-18 | 2023-06-23 | 安徽火峰电气有限公司 | 一种防凝露阻燃聚氨酯密封件及其制备方法 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001040275A (ja) * | 1999-07-28 | 2001-02-13 | Nippon Paint Co Ltd | ホログラム層形成用樹脂組成物、ホログラム記録用媒体およびホログラム記録物 |
| EP1243606A1 (en) * | 2001-03-19 | 2002-09-25 | Four Trend, Inc. | A resin composition for forming a matte-finished surface and a method of forming a matte-finished surface |
| US6743552B2 (en) * | 2001-08-07 | 2004-06-01 | Inphase Technologies, Inc. | Process and composition for rapid mass production of holographic recording article |
| US6765061B2 (en) * | 2001-09-13 | 2004-07-20 | Inphase Technologies, Inc. | Environmentally durable, self-sealing optical articles |
-
2008
- 2008-03-28 CN CN200880011796A patent/CN101657483A/zh active Pending
- 2008-03-28 BR BRPI0809620-1A patent/BRPI0809620A2/pt not_active IP Right Cessation
- 2008-03-28 KR KR1020097021129A patent/KR20100015472A/ko not_active Application Discontinuation
- 2008-03-28 EP EP08734842A patent/EP2144946A1/en not_active Withdrawn
- 2008-03-28 CA CA002683902A patent/CA2683902A1/en not_active Abandoned
- 2008-03-28 JP JP2010502439A patent/JP2010523776A/ja not_active Withdrawn
- 2008-03-28 RU RU2009141370/04A patent/RU2009141370A/ru not_active Application Discontinuation
- 2008-03-28 WO PCT/EP2008/002467 patent/WO2008125202A1/en active Application Filing
- 2008-04-10 TW TW097112924A patent/TW200906882A/zh unknown
- 2008-04-10 US US12/100,783 patent/US20080311483A1/en not_active Abandoned
-
2009
- 2009-09-17 IL IL201036A patent/IL201036A0/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US20080311483A1 (en) | 2008-12-18 |
| IL201036A0 (en) | 2010-05-17 |
| TW200906882A (en) | 2009-02-16 |
| KR20100015472A (ko) | 2010-02-12 |
| JP2010523776A (ja) | 2010-07-15 |
| BRPI0809620A2 (pt) | 2014-09-16 |
| CN101657483A (zh) | 2010-02-24 |
| EP2144946A1 (en) | 2010-01-20 |
| WO2008125202A1 (en) | 2008-10-23 |
| CA2683902A1 (en) | 2008-10-23 |
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