Polycarbonate resin and method for producing the same
A technology of polycarbonate resin and manufacturing method, applied in the field of optical materials, capable of solving problems such as inability to obtain satisfactory molded products, coloring, insufficient formability and heat resistance, etc.
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[0171] The present invention will be described below through examples, but the present invention is not limited by these examples. In addition, the measured value in an Example was measured using the following method or apparatus.
[0172] 1) Intrinsic viscosity (limiting viscosity): Ubbelohde viscosity tube is used. Measurement was performed at 20° C., 0.5% dichloromethane solution, and a Huggins constant of 0.45.
[0173] 2) Glass transition temperature (Tg): measured by a differential scanning calorimeter (DSC).
[0174] 3) Photoelastic coefficient: Calculated by ellipsometry, using a cast film with a thickness of 100 μm, irradiating light with a laser wavelength of 633 nm, and measuring birefringence with respect to load changes.
[0175] 4) Film strength and elongation: Based on ASTM D882-61T, the tensile strength and tensile elongation of the 100-micrometer-thick film obtained in the Example were measured using Shimadzu Autograph AGS-100G.
[0176] 5) Total light tran...
Synthetic example 1
[0180] Add 308g of acenaphthene, 3250mL of acetic acid, 30.6g of cobalt(II) bromide hexahydrate, 6.1g of cobalt(II) acetate tetrahydrate, and 1.5g of manganese(II) acetate tetrahydrate into a 10L three-necked flask, stir and mix , after completely dissolving it, air was blown into the solution at 20° C. under normal pressure at 400 L / h. After 4.3 hours, the reaction was stopped, and the reaction product was analyzed by a gas chromatograph. As a result, the conversion of acenaphthene was 99.2%, and the yield of acenaphth-1-one was 28.1%.
Synthetic example 2
[0182] 1 L of toluene and 2 L of water were added to 1 kg of the reaction product liquid obtained in Synthesis Example 1, stirred for 5 minutes and extracted, then left to stand for 15 to 20 minutes, separated, and the upper toluene layer was recovered. Put 4% aqueous sodium hydroxide solution equivalent to the above extract into a separatory funnel, shake and let it stand, and remove the black liquid in the lower layer. The same amount of water as the remaining solution was added and washed to remove the lower layer liquid. Further, water was added, 2 mL of hydrochloric acid was added, and the mixture was shaken to remove the liquid in the lower layer, followed by washing with water again. The oil layer was further washed with alkali, concentrated, and the solvent was removed. The concentrated solution was distilled at a pressure of 1 to 2 mmHg, and 16 g of acenaphth-1-one was distilled at a distillation temperature of 120°C.
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