JP2013530294A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2013530294A5 JP2013530294A5 JP2013518491A JP2013518491A JP2013530294A5 JP 2013530294 A5 JP2013530294 A5 JP 2013530294A5 JP 2013518491 A JP2013518491 A JP 2013518491A JP 2013518491 A JP2013518491 A JP 2013518491A JP 2013530294 A5 JP2013530294 A5 JP 2013530294A5
- Authority
- JP
- Japan
- Prior art keywords
- composition according
- composition
- ester compound
- cyclic ester
- divinylarene dioxide
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 claims description 36
- -1 cyclic ester compound Chemical class 0.000 claims description 18
- 239000012952 cationic photoinitiator Substances 0.000 claims description 8
- 239000000463 material Substances 0.000 claims description 8
- 239000000049 pigment Substances 0.000 claims description 8
- YDIZFUMZDHUHSH-UHFFFAOYSA-N 1,7-bis(ethenyl)-3,8-dioxatricyclo[5.1.0.02,4]oct-5-ene Chemical class C12OC2C=CC2(C=C)C1(C=C)O2 YDIZFUMZDHUHSH-UHFFFAOYSA-N 0.000 claims description 6
- 150000001450 anions Chemical class 0.000 claims description 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 4
- JBFHTYHTHYHCDJ-UHFFFAOYSA-N gamma-caprolactone Chemical compound CCC1CCC(=O)O1 JBFHTYHTHYHCDJ-UHFFFAOYSA-N 0.000 claims description 4
- JJTUDXZGHPGLLC-UHFFFAOYSA-N lactide Chemical compound CC1OC(=O)C(C)OC1=O JJTUDXZGHPGLLC-UHFFFAOYSA-N 0.000 claims description 4
- ILSRXKFYTXYKJS-UHFFFAOYSA-N 2,4-bis(ethenyl)-3,6-dioxatetracyclo[6.4.0.02,4.05,7]dodeca-1(12),8,10-triene Chemical class C=CC12OC1(C=C)C1=CC=CC=C1C1C2O1 ILSRXKFYTXYKJS-UHFFFAOYSA-N 0.000 claims description 2
- GLPDXGJXUWGMQJ-UHFFFAOYSA-N 4-ethenyl-7-(4-ethenylphenyl)-3,8-dioxatricyclo[5.1.0.02,4]oct-5-ene Chemical class C(=C)C1=CC=C(C=C1)C12C(C3C(C=C1)(C=C)O3)O2 GLPDXGJXUWGMQJ-UHFFFAOYSA-N 0.000 claims description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 2
- 229910018286 SbF 6 Inorganic materials 0.000 claims description 2
- PFHLXMMCWCWAMA-UHFFFAOYSA-N [4-(4-diphenylsulfoniophenyl)sulfanylphenyl]-diphenylsulfanium Chemical compound C=1C=C([S+](C=2C=CC=CC=2)C=2C=CC=CC=2)C=CC=1SC(C=C1)=CC=C1[S+](C=1C=CC=CC=1)C1=CC=CC=C1 PFHLXMMCWCWAMA-UHFFFAOYSA-N 0.000 claims description 2
- 239000001055 blue pigment Substances 0.000 claims description 2
- VVOLVFOSOPJKED-UHFFFAOYSA-N copper phthalocyanine Chemical compound [Cu].N=1C2=NC(C3=CC=CC=C33)=NC3=NC(C3=CC=CC=C33)=NC3=NC(C3=CC=CC=C33)=NC3=NC=1C1=CC=CC=C12 VVOLVFOSOPJKED-UHFFFAOYSA-N 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- 230000003301 hydrolyzing effect Effects 0.000 claims description 2
- 150000002596 lactones Chemical class 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 claims description 2
- 229920005862 polyol Polymers 0.000 claims description 2
- 150000003077 polyols Chemical class 0.000 claims description 2
- 239000004408 titanium dioxide Substances 0.000 claims description 2
- 239000012953 triphenylsulfonium Substances 0.000 claims description 2
- 239000004034 viscosity adjusting agent Substances 0.000 claims description 2
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 claims description 2
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 150000002118 epoxides Chemical class 0.000 description 2
- AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridin-1-ium;chloride Chemical compound [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- BSCHIACBONPEOB-UHFFFAOYSA-N oxolane;hydrate Chemical compound O.C1CCOC1 BSCHIACBONPEOB-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US35910110P | 2010-06-28 | 2010-06-28 | |
| US61/359,101 | 2010-06-28 | ||
| PCT/US2011/041566 WO2012009120A2 (en) | 2010-06-28 | 2011-06-23 | Curable resin compositions |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013530294A JP2013530294A (ja) | 2013-07-25 |
| JP2013530294A5 true JP2013530294A5 (https=) | 2014-08-07 |
| JP5778768B2 JP5778768B2 (ja) | 2015-09-16 |
Family
ID=44628207
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013518491A Expired - Fee Related JP5778768B2 (ja) | 2010-06-28 | 2011-06-23 | 硬化性樹脂組成物 |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US20130090407A1 (https=) |
| EP (1) | EP2585536B1 (https=) |
| JP (1) | JP5778768B2 (https=) |
| CN (1) | CN102985459A (https=) |
| TW (1) | TWI540147B (https=) |
| WO (1) | WO2012009120A2 (https=) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20130090407A1 (en) * | 2010-06-28 | 2013-04-11 | James Wells Carter | Curable resin compositions |
| EP2786878A1 (en) * | 2013-04-04 | 2014-10-08 | Hewlett-Packard Industrial Printing Ltd. | Methods for printing articles |
| JP6568218B2 (ja) | 2014-12-23 | 2019-08-28 | ブリヂストン アメリカズ タイヤ オペレーションズ、 エルエルシー | 化学線硬化型高分子混合物、硬化高分子混合物、及び関連するプロセス |
| US10442941B2 (en) * | 2015-03-20 | 2019-10-15 | Blue Cube Ip Llc | Curable compositions |
| JP7160532B2 (ja) * | 2015-03-20 | 2022-10-25 | ブルー キューブ アイピー エルエルシー | 硬化性組成物 |
| US11097531B2 (en) | 2015-12-17 | 2021-08-24 | Bridgestone Americas Tire Operations, Llc | Additive manufacturing cartridges and processes for producing cured polymeric products by additive manufacturing |
| US11453161B2 (en) | 2016-10-27 | 2022-09-27 | Bridgestone Americas Tire Operations, Llc | Processes for producing cured polymeric products by additive manufacturing |
| US11773253B2 (en) * | 2016-12-09 | 2023-10-03 | Lg Chem, Ltd. | Encapsulating composition |
| SE1730346A1 (en) * | 2017-12-19 | 2019-06-11 | Perstorp Ab | A hybrid photopolymer composition for additive manufacturing |
| US11633908B2 (en) * | 2018-03-02 | 2023-04-25 | Formlabs, Inc. | Latent cure resins and related methods |
| KR102532383B1 (ko) * | 2018-08-08 | 2023-05-12 | 아사히 가세이 가부시키가이샤 | 에어백용 다층 필름 및 에어백 |
| JP7345750B2 (ja) * | 2019-03-15 | 2023-09-19 | 株式会社レゾナック | エポキシ樹脂組成物、エポキシ樹脂硬化物及びエポキシ樹脂改質剤 |
| EP4157905A4 (en) * | 2020-06-02 | 2024-05-15 | Blue Cube IP LLC | PHOTOCURABLE RESIN COMPOSITION FOR USE IN STEREOLITHOGRAPHY |
| WO2025035415A1 (en) * | 2023-08-16 | 2025-02-20 | Dow Global Technologies Llc | Solvent-free high refractive index uv curable epoxy ink compositions |
Family Cites Families (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL128404C (https=) | 1959-12-24 | |||
| US4058401A (en) | 1974-05-02 | 1977-11-15 | General Electric Company | Photocurable compositions containing group via aromatic onium salts |
| US4161478A (en) | 1974-05-02 | 1979-07-17 | General Electric Company | Photoinitiators |
| US4058400A (en) | 1974-05-02 | 1977-11-15 | General Electric Company | Cationically polymerizable compositions containing group VIa onium salts |
| US4175972A (en) | 1974-05-02 | 1979-11-27 | General Electric Company | Curable epoxy compositions containing aromatic onium salts and hydroxy compounds |
| US4105806A (en) | 1976-11-19 | 1978-08-08 | American Can Company | Photoinitiator free inks and method |
| US4138255A (en) | 1977-06-27 | 1979-02-06 | General Electric Company | Photo-curing method for epoxy resin using group VIa onium salt |
| US4273668A (en) | 1977-09-14 | 1981-06-16 | General Electric Company | Arylsulfonium salt-solvent mixtures |
| US4231951A (en) | 1978-02-08 | 1980-11-04 | Minnesota Mining And Manufacturing Company | Complex salt photoinitiator |
| US4173476A (en) | 1978-02-08 | 1979-11-06 | Minnesota Mining And Manufacturing Company | Complex salt photoinitiator |
| US4186108A (en) | 1978-02-08 | 1980-01-29 | Minnesota Mining And Manufacturing Company | Liquid compositions containing triarylsulfonium complex salts and oxyethylene material |
| US4218531A (en) | 1978-02-08 | 1980-08-19 | Minnesota Mining And Manufacturing Company | Addition of ethylenically unsaturated materials to control odor in photopolymerizable epoxy compositions |
| US4201640A (en) | 1979-03-14 | 1980-05-06 | American Can Company | Method for producing bis-[4-(diphenylsulfonio)phenyl] sulfide bis-M.X6 |
| US4197174A (en) | 1979-03-14 | 1980-04-08 | American Can Company | Method for producing bis-[4-(diphenylsulfonio) phenyl] sulfide bis-MX6 |
| US4247473A (en) | 1979-07-19 | 1981-01-27 | American Can Company | Method for producing bis-[4-(diphenylsulfonio)pheny] sulfide bis-M.X6 photoinitiator |
| US4247472A (en) | 1979-07-19 | 1981-01-27 | American Can Company | Method for producing bis-[4-(diphenylsulfonic)phenyl]sulfide bis-MF6 photoinitiator |
| DE69520222T2 (de) * | 1994-10-31 | 2001-08-23 | Minnesota Mining And Mfg. Co., Saint Paul | Mit sichtbarem licht härtbares epoxysystem mit verbesserter härtungstiefe |
| JPH1161078A (ja) * | 1997-01-20 | 1999-03-05 | Nippon Kayaku Co Ltd | 接着剤組成物、接着体、接着方法及び光ディスクの製造方法 |
| US6020508A (en) * | 1997-05-16 | 2000-02-01 | National Starch And Chemical Investment Holding Corporation | Radiation- or thermally-initiated cationically-curable epoxide compounds and compositions made from those compounds |
| AU711786B2 (en) | 1997-05-16 | 1999-10-21 | National Starch And Chemical Investment Holding Corporation | Reactive radiation- or thermally-initiated cationically- curable epoxide monomers and compositions made from those monomers |
| ES2126545T1 (es) * | 1997-05-16 | 1999-04-01 | Nat Starch Chem Invest | Monomeros de epoxido reactivos curables cationicamente iniciados termicamente o por radiacion, y composiciones realizadas a partir de estos monomeros. |
| JPH1143660A (ja) * | 1997-07-25 | 1999-02-16 | Nippon Kayaku Co Ltd | 接着剤組成物及び接着方法 |
| JP2002148799A (ja) * | 2000-11-14 | 2002-05-22 | Mitsubishi Gas Chem Co Inc | 耐燃性に優れたレジスト組成物 |
| GB0204468D0 (en) | 2002-02-26 | 2002-04-10 | Coates Brothers Plc | Novel thioxanthone derivatives, and their use as cationic photoinitiators |
| GB0204467D0 (en) | 2002-02-26 | 2002-04-10 | Coates Brothers Plc | Novel fused ring compounds, and their use as cationic photoinitiators |
| KR100502993B1 (ko) * | 2002-03-08 | 2005-07-25 | 주식회사 루밴틱스 | 광통신부품용 광학접착제 |
| GB2396153A (en) | 2002-12-12 | 2004-06-16 | Sun Chemical Bv | Sulfonium salts useful as cationic photoinitiators in energy-curable compositions and processes of preparing cured polymeric compositions |
| US7309122B2 (en) | 2003-06-24 | 2007-12-18 | Konica Minolta Medical & Graphic, Inc. | Method for storing cationic polymerizable composition and container for using thereof |
| GB2420782A (en) | 2004-12-01 | 2006-06-07 | Sun Chemical Ltd | Cationically curable coating compositions |
| US20070213429A1 (en) * | 2006-03-10 | 2007-09-13 | Chih-Min Cheng | Anisotropic conductive adhesive |
| KR101403187B1 (ko) * | 2008-02-19 | 2014-06-02 | 삼성전자주식회사 | 감광성 조성물, 이를 이용한 미세 가공 방법 및 그에 의해형성된 미세 가공물 |
| CN101431145B (zh) * | 2008-12-08 | 2010-06-02 | 电子科技大学 | 一种柔性有机光电子器件用基板及其制备方法 |
| US20130090407A1 (en) * | 2010-06-28 | 2013-04-11 | James Wells Carter | Curable resin compositions |
-
2011
- 2011-06-23 US US13/701,837 patent/US20130090407A1/en not_active Abandoned
- 2011-06-23 EP EP20110730806 patent/EP2585536B1/en not_active Not-in-force
- 2011-06-23 WO PCT/US2011/041566 patent/WO2012009120A2/en not_active Ceased
- 2011-06-23 CN CN2011800321295A patent/CN102985459A/zh active Pending
- 2011-06-23 JP JP2013518491A patent/JP5778768B2/ja not_active Expired - Fee Related
- 2011-06-27 TW TW100122395A patent/TWI540147B/zh not_active IP Right Cessation
-
2016
- 2016-02-05 US US15/017,162 patent/US20160152846A1/en not_active Abandoned
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2013530294A5 (https=) | ||
| JP2013531721A5 (https=) | ||
| Santiago et al. | New epoxy thermosets derived from clove oil prepared by epoxy-amine curing | |
| JP6650402B2 (ja) | イソヘキシドグリシジルエーテルを生成する方法、それにより得られる生成物の使用 | |
| Alrahlah et al. | A low-viscosity BisGMA derivative for resin composites: synthesis, characterization, and evaluation of its rheological properties | |
| JP2010168554A5 (https=) | ||
| Guzmán et al. | Novel bio-based epoxy thermosets based on triglycidyl phloroglucinol prepared by thiol-epoxy reaction | |
| BR112013003299A8 (pt) | Processo para preparar uma resina epóxi alifática ou cicloalifática | |
| Sowińska et al. | Bis (trifluoromethylsulfonyl) imide ionic liquids applied for fine-tuning the cure characteristics and performance of natural rubber composites | |
| Okeke et al. | Synthesis, purification and characterization of polymerizable multifunctional quaternary ammonium compounds | |
| Wu et al. | Silicone-thioxanthone: A multifunctionalized visible light photoinitiator with an ability to modify the cured polymers | |
| Tikhani et al. | Polyurethane/silane-functionalized ZrO2 nanocomposite powder coatings: Thermal degradation kinetics | |
| Sarychev et al. | Synthesis of resorcinol-based phosphazene-containing epoxy oligomers | |
| Song et al. | The facile strategy of improving the long-term stability of highly transparent polyvinyl chloride by introducing unsaturated Zn oleate and uracil derivatives | |
| Hu et al. | Synthesis of Hyperbranched flame retardants with varied branched chains’ rigidity and performance of modified epoxy resins | |
| Alshabebi et al. | Preparation of bio-based polyurethane coating from citrullus colocynthis seed oil: characterization and corrosion performance | |
| Puglisi et al. | Photo-and water-degradation phenomena of ZnO bio-blend based on poly (lactic acid) and polyamide 11 | |
| Tryznowski et al. | Surface properties of poly (hydroxyurethane) s based on five-membered bis-cyclic carbonate of diglycidyl ether of bisphenol A | |
| Zhao et al. | Preparation and characterization of fluorinated acrylate and epoxy co-modified waterborne polyurethane | |
| Li et al. | Synthesis and Properties of the Novel High-Performance Hydroxyl-Terminated Liquid Fluoroelastomer | |
| WO2017142089A1 (ja) | 化合物及び発光材料 | |
| JP2001342194A (ja) | 多官能オキセタン化合物およびその製造方法、ならびに該オキセタン化合物からなるカチオン硬化性組成物 | |
| Liu et al. | Effect of lithium mica slag on the internal sulfate attack of cement mortar | |
| Silva et al. | Valorisation of recycled cement paste: feasibility of a short-duration carbonation process | |
| Byczyński et al. | Influence of a Siloxane-Modified DOPO Derivative on the Properties of Polyurethane Cationomer Coatings |