Curable composition, cured film, display device and dry film
A technology of curable composition and cured film, which is applied in the fields of nonlinear optics, optics, and optomechanical equipment, and can solve problems such as longer production intervals, lower solubility of coating films in alkaline developer solutions, lower product yields, etc. , to achieve the effect of excellent developability
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[0246] Hereinafter, an embodiment of the present invention will be described in more detail by way of examples. However, the present invention is not limited to the following examples.
[0247]
[0248] Mw and Mn of the polymers obtained in the following synthesis examples were measured by gel permeation chromatography (hereinafter, abbreviated as GPC) in the following format.
[0249] Device: GPC-104 (manufactured by Showa Denko Co., Ltd.).
[0250] Column: Use KD-G, KF-603, KF-602, and KF-601 in combination.
[0251] Mobile phase: tetrahydrofuran.
[0252]
[0253] The acid value of the polymer obtained in each synthesis example below was measured by the following method.
[0254] Weigh 0.5 g of the polymer solution to an accuracy of 1 mg, and dispense into glass containers. After diluting to 50 mL with propylene glycol monomethyl ether acetate, phenolphthalein was added and titrated with a 0.1N ethanolic potassium hydroxide aqueous solution, and the point where it w...
Synthetic example 1
[0259] 194.4 parts by mass of cyclohexanone were placed in a flask equipped with a cooling tube and a stirrer, and nitrogen substitution was performed. Heated to 80°C, and at this temperature, 60 parts by mass of propylene glycol monomethyl ether acetate, 60 parts by mass of methacrylic acid, 30 parts by mass of butyl methacrylate, EO modified 2-ethyl acrylic acid A mixed solution of 30 parts by mass of methylhexyl ester (manufactured by Toagosei Co., Ltd., M-120) and 18 parts by mass of cyclohexyl methacrylate, and 45.6 parts by mass of propylene glycol monomethyl ether and 2,2'-azobis(2, 4-Dimethylvaleronitrile) 10.8 parts by mass of the mixed solution, and kept the temperature for polymerization for 1 hour. Thereafter, the temperature of the reaction solution was raised to 90° C., followed by polymerization for 1 hour, whereby a resin (1) solution was obtained. The obtained resin (1) had Mw=8300, Mn=4500, and Mw / Mn=1.84.
[0260] 374.0 parts by mass of the resin (1) solut...
Synthetic example 2
[0262]1216 parts by mass of cyclohexanone were placed in a flask equipped with a cooling tube and a stirrer, and nitrogen substitution was performed. Heated to 80°C, and at this temperature, 160 parts by mass of cyclohexanone, 160 parts by mass of butyl methacrylate, and EO-modified 2-ethylhexyl acrylate (manufactured by Toagosei Co., Ltd., M -120) 160 parts by mass, Tricyclic-[5.2.1.0 2,6 A mixed solution of 120 parts by mass of ]-decyl (meth)acrylate and 480 parts by mass of glycidyl methacrylate and 224 parts by mass of cyclohexanone and 2,2'-azobis(2,4-dimethyl valeronitrile) 56 parts by mass of a mixed solution, and kept the temperature for polymerization for 1 hour. Thereafter, the temperature of the reaction solution was raised to 90° C., and polymerization was carried out for an additional hour to obtain a resin (2) solution. The obtained resin (2) had Mw=7200, Mn=4000, and Mw / Mn=1.80.
[0263] 966 parts by mass of the resin (2) solution, 6.15 parts by mass of tetra...
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