Curable resin composition, cured article and optical artical
A curable resin and composition technology, applied in optics, optical components, instruments, etc., can solve the problems of low water absorption of optical properties, heat resistance of formability, surface hardness, accuracy of optical surface shape, insufficient toughness, etc. , to achieve the effect of surface hardness and precision metal mold transfer improvement, low water absorption, excellent optical properties
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[0080] Next, the present invention will be described by way of examples, but the present invention is not limited thereto. In addition, the parts in each example are parts by weight unless otherwise specified. In addition, about the measurement of the softening temperature etc. in an Example, sample preparation and measurement were performed by the method shown below.
[0081] (Measurement of physical properties of copolymers and their cured products)
[0082] 1) Molecular weight and molecular weight distribution of the polymer
[0083] The molecular weight and molecular weight distribution of the soluble polyfunctional copolymer were measured using GPC (manufactured by Tosoh, HLC-8120GPC) with tetrahydrofuran (THF) as the solvent, 1.0 ml / min flow rate, and 40° C. column temperature. The molecular weight of the copolymer was measured as a polystyrene-equivalent molecular weight using a calibration curve using monodisperse polystyrene.
[0084] 2) The structure of the polyme...
Synthetic example 1
[0128] Dimethylol tricyclodecane diacrylate 1.6mol (463.2ml), dicyclopentyl methacrylate 1.2mol (254.2ml), 1,4-butanediol diacrylate 1.2mol (226.3ml) , 2,4-diphenyl-4-methyl-1-pentene (0.4mol (95.5ml), tertiary dodecyl mercaptan 2.4mol (564.8ml), toluene 600ml into a 3.0L reactor , Add 40mmol (11.5g) of tert-butyl peroxy-2-ethylhexanoate at 90°C and allow it to react for 2 hours and 45 minutes. After the polymerization reaction is stopped by cooling, the reaction mixture is put into The copolymer was precipitated in a large amount of hexane. The obtained copolymer was washed with hexane, filtered, dried, and weighed to obtain 691.0 g of copolymer A.
[0129] Mw of the obtained copolymer A was 34200, Mn was 5620, and Mw / Mn was 6.1. by carrying out 13 C-NMR, 1 H-NMR analysis and elemental analysis, copolymer A contains a total of 39.6 mol% of structural units (1) derived from dimethyloltricyclodecane diacrylate, a total of 31.1 mol% of dicyclopentanyl methacrylate derived fro...
Synthetic example 2
[0132] Dimethyloltricyclodecane diacrylate 2.64mol (764.3ml), dicyclopentyl acrylate 0.24mol (47.2ml), 1,4-butanediol diacrylate 0.96mol (181.0ml), acrylic acid 0.96mol (118.5ml) of 2-hydroxypropyl ester, 0.48mol (114.6ml) of 2,4-diphenyl-4-methyl-1-pentene, 3.12mol (734.3ml) of tert-dodecyl mercaptan, 720 ml of toluene was put into a 3.0 L reactor, and 62 mmol (13.9 g) of tert-butylperoxy-2-ethylhexanoate was added at 90° C., and reacted for 2 hours and 30 minutes. After the polymerization reaction was stopped by cooling, the reaction mixture was poured into a large amount of hexane at room temperature to precipitate a copolymer. The obtained copolymer was washed with hexane, filtered, dried, and weighed to obtain 782.2 g of copolymer B.
[0133] Copolymer B was tested in the same manner as copolymer A, and the results are shown in Table 1.
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