Resin composition, optical compensation film using same, and manufacturing method thereof
A technology of resin composition and optical compensation film, which is applied in optics, optical components, nonlinear optics, etc., and can solve the problems that retardation plates cannot meet Re and Nz
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[0118] Hereinafter, the present invention will be described with reference to examples, but the present invention is not limited to these examples.
[0119] In addition, various physical properties shown in Examples were measured by the following methods.
[0120]
[0121] The structural analysis of the polymer was carried out by proton nuclear magnetic resonance emission ( 1 H-NMR) spectrum analysis.
[0122]
[0123] A gel permeation chromatography (GPC) apparatus (manufactured by Tosoh, trade name: C0-8011 (column GMH) was used. HR -H)), measured at 40°C using tetrahydrofuran or dimethylformamide as a solvent, and obtained as standard polystyrene conversion.
[0124]
[0125] Regarding the measurement of the light transmittance and haze of the produced film, the light transmittance was measured according to JIS K7361-1 (1997 edition), and the haze was measured using a haze meter (manufactured by Nippon Denshoku Industries, trade name: NDH2000) according to JIS-K713...
Synthetic example 1
[0130] Synthesis Example 1 (Synthesis of Diethyl Fumarate Polymer)
[0131] 50 g of diethyl fumarate and 0.45 g of t-butyl peroxypivalate as a polymerization initiator were placed in a glass ampoule with a capacity of 75 mL, nitrogen substitution and pressure relief were repeated, and then the mixture was sealed under reduced pressure. The ampoule was placed in a thermostat at 50°C, and radical polymerization was carried out by holding it for 72 hours. After the completion of the polymerization reaction, the polymer was taken out from the ampoule and dissolved in 200 g of tetrahydrofuran. This polymer solution was dripped in 4 L of hexane and precipitated, and then vacuum-dried at 80° C. for 10 hours to obtain 26 g of a diethyl fumarate polymer. The number average molecular weight of the obtained polymer was 25,000.
Synthetic example 2
[0132] Synthesis Example 2 (Synthesis of Diethyl Fumarate / Monoethyl Fumarate Copolymer)
[0133] 48 g of diethyl fumarate, 2.1 g of monoethyl fumarate, and 0.45 g of t-butyl peroxypivalate as a polymerization initiator were placed in a glass ampoule with a capacity of 75 mL, and nitrogen substitution and pressure relief were repeated. , melted under reduced pressure. The ampoule was placed in a thermostat at 50°C, and radical polymerization was carried out by holding it for 72 hours. After the completion of the polymerization reaction, the polymer was taken out from the ampoule and dissolved in 200 g of tetrahydrofuran. 22 g of diethyl fumarate / monoethyl fumarate copolymers were obtained by dripping this polymer solution in 4 L of hexane and making it precipitate, and vacuum-dried at 80 degreeC for 10 hours. The obtained polymer had a number average molecular weight of 23,000, 95 mol % of diethyl fumarate residue units, and 5 mol % of monoethyl fumarate residue units.
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