Light curable resin composition
US-2017029671-A1 · Feb 2, 2017 · US
US11739168B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11739168-B2 |
| Application number | US-201816642530-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 31, 2018 |
| Priority date | Sep 1, 2017 |
| Publication date | Aug 29, 2023 |
| Grant date | Aug 29, 2023 |
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Conventionally, a photocurable composition to which an ultraviolet absorber is added is difficult to form a colorless and transparent cured resin because the ultraviolet absorber itself is colored, and thus the photocurable composition is hardly to be used in a display apparatus required for colorlessness and transparency. Provided is a photocurable composition including a specific compound, wherein a light transmittance of 385 nm is 50% or less and a yellowness index is 3.0 or less in a state in which a cured resin having a thickness of 200 μm or less is interposed between alkali free glass plates each having a thickness of 0.7 mm.
Opening claim text (preview).
The invention claimed is: 1. A photocurable composition comprising a compound of the following General Formula 1 or 2-(2′-hydroxy-3′-tert-butyl-5′-methylphenyl)-5-chlorobenzotriazole as a component (A), a (meth)acrylate compound as a component (B); a film-forming resin as a component (C); and a photoinitiator as a component (D), wherein a light transmittance of 385 nm is 50% or less and a yellowness index is 3.0 or less in a state in which a cured resin of the photocurable composition with a thickness of 200 μm or less is interposed between alkali free glass plates each having a thickness of 0.7 mm: n is an integer of 1 to 4, R is a hydrocarbon group having a total number of carbon atoms of 6 or more, and hydrogen in a main skeleton of the compound may be substituted with another organic group, where a multimer is excluded. 2. The photocurable composition according to claim 1 , wherein a light transmittance of 385 nm is 30% or less and a yellowness index is 3.0 or less in a state in which a cured resin of the photocurable composition with a thickness of 200 μm or less is interposed between alkali free glass plates each having a thickness of 0.7 mm. 3. The photocurable composition according to claim 1 , wherein the component (B) includes a (meth)acrylate oligomer and a (meth)acrylate monomer. 4. The photocurable composition according to claim 3 , wherein the (meth)acrylate oligomer is a urethane-modified (meth)acrylate oligomer. 5. The photocurable composition according to claim 4 , wherein a main skeleton of the urethane-modified (meth)acrylate oligomer is polycarbonate. 6. The photocurable composition according to claim 3 , wherein a main skeleton of the (meth)acrylate monomer is polyether. 7. The photocurable composition according to claim 1 , wherein the component (C) is a phenoxy resin. 8. The photocurable composition according to claim 1 , wherein the component (D) includes an acylphosphineoxide-based photoinitiator. 9. The photocurable composition according to claim 1 , wherein a content of the component (A) is 0.1 to 4.0% by mass with respect to a total composition excluding a solvent. 10. The photocurable composition according to claim 1 , wherein the photocurable composition is used in assembling an organic EL device. 11. A photocurable sheet comprising the photocurable composition set forth in claim 1 . 12. A display apparatus using the photocurable composition set forth in claim 1 . 13. An adhering method comprising: a step of attaching the photocurable sheet set forth in claim 11 to one adherend and sticking another adherend to the photocurable sheet; and a step of curing the photocurable sheet by irradiation with an energy ray to adhere the two adherends. 14. A method of producing a display apparatus comprising the adhering method set forth in claim 13 . 15. The photocurable composition according to claim 1 , which comprises the compound of the General Formula 1 or 2-(T-hydroxy-3′-tert-butyl-5′-methylphenyl)-5-chlorobenzotriazole as a component (A), and when the component (A) is 2-(T-hydroxy-3′-tert-butyl-5′-methylphenyl)-5-chlorobenzotriazole, a content of the component (A) is 0.1 to 1.1% by mass with respect to a total composition excluding a solvent. 16. The photocurable composition according to claim 1 , which comprises 2-(2′-hydroxy-5′-tert-octylphenyl)benzotriazole, 2-(2′-hydroxy-3′-tert-butyl-5′-methylphenyl)-5-chlorobenzotriazole, or 2-(3,5-di-tert-amyl-2-hydroxyphenyl)benzotriazole as a component (A), and when the component (A) is 2-(2′-hydroxy-3′-tert-butyl-5′-methylphenyl)-5-chlorobenzotriazole, a content of the component (A) is 0.1 to 1.1% by mass with respect to a total composition excluding a solvent.
Forming devices by joining two substrates together, e.g. lamination techniques · CPC title
Manufacture or treatment specially adapted for the organic devices covered by this subclass · CPC title
by ultraviolet or visible light · CPC title
Encapsulations · CPC title
containing aliphatic unsaturation · CPC title
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