Optical resin composition and film
US-2017031058-A1 · Feb 2, 2017 · US
US11286237B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11286237-B2 |
| Application number | US-202016920753-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 6, 2020 |
| Priority date | Aug 30, 2016 |
| Publication date | Mar 29, 2022 |
| Grant date | Mar 29, 2022 |
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Provided is a method for manufacturing a methacrylic resin composition having excellent surface processability and displaying excellent preservability of formed surface processing. A method for manufacturing a methacrylic resin composition, wherein the methacrylic resin composition comprises two or more types of methacrylic resins that each have a structural unit (X) having the same type of cyclic structure-containing main chain, the methacrylic resin composition has a Vicat softening temperature of 120° C. to 160° C., methanol-soluble content is contained in an amount of 5 mass % or less relative to 100 mass %, in total, of the methanol-soluble content and methanol-insoluble content, comprising mixing a low molecular weight component and a high molecular weight component.
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The invention claimed is: 1. A method for manufacturing a methacrylic resin composition, the method comprising: mixing a low molecular weight methacrylic resin having a weight average molecular weight (Mw) of 70,000 to 157,000 and a ratio (S/H) of integrated intensity (S) of a syndiotactic fraction (rr) relative to integrated intensity (H) of a heterotactic fraction (mr), as determined by 1 H-NMR measurement, is 1.10 to 1.40, and a high molecular weight methacrylic resin having a weight average molecular weight (Mw) of 185,000 to 800,000 and a ratio (S/H) of integrated intensity (S) of a syndiotactic fraction (rr) relative to integrated intensity (H) of a heterotactic fraction (mr), as determined by 1 H-NMR measurement, is 1.30 to 1.95, wherein the low molecular weight methacrylic resin and the high molecular weight methacrylic resin each have a structural unit (X) having same cyclic structure-containing main chain and said cyclic structure-containing main chain includes a lactone ring structural unit, the methacrylic resin composition comprises the low molecular weight methacrylic resin and the high molecular weight methacrylic resin, the methacrylic resin composition has a Vicat softening temperature of 120° C. to 160° C., methanol-soluble content is contained in an amount of 5 mass % or less relative to 100 mass %, in total, of the methanol-soluble content and methanol-insoluble content, and a total content of the lactone ring structural units is 5 mass % to 40 mass % relative to 100 mass % of the methacrylic resin composition. 2. The method for manufacturing a methacrylic resin composition according to claim 1 , wherein the methacrylic resin composition has a weight average molecular weight (Mw) of 120,000 to 200,000 as measured by gel permeation chromatography as a polymethyl methacrylate equivalent molecular weight. 3. The method for manufacturing a methacrylic resin composition according to claim 1 , wherein the methacrylic resin composition has a photoelastic coefficient with an absolute value of 2.0×10 −12 Pa −1 or less. 4. The method for manufacturing a methacrylic resin composition according to claim 3 , wherein the methacrylic resin composition has a photoelastic coefficient with an absolute value of 1.0×10 −12 Pa −1 or less.
with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms, e.g. maleimide · CPC title
Homopolymers or copolymers of amides or imides · CPC title
Methyl esters {, e.g. methyl (meth)acrylate} · CPC title
Homopolymers or copolymers of methacrylic acid esters · CPC title
Copolymers with vinyl aromatic monomers · CPC title
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