Curable composition, cured article, and use of curable composition
A technology of curable composition and cured product, which can be applied in the direction of adhesive type, electric solid device, semiconductor/solid device manufacturing, etc., can solve the problems of inability to meet the light deterioration resistance, decreased adhesion, etc., and achieve excellent transparency , the effect of high adhesion
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[0216] Hereinafter, the present invention will be described in more detail by way of examples and comparative examples, but the present invention is not limited to the following examples.
[0217] (Determination of weight average molecular weight)
[0218] The weight average molecular weight (Mw) of the silane compound copolymer obtained in the manufacture example was measured with the following apparatus and conditions as a standard polystyrene conversion value.
[0219] Device name: HLC-8220GPC, manufactured by Tosoh Corporation
[0220] Column: Connect TSKgelGMHXL, TSKgelGMHXL and TSKgel2000HXL in sequence
[0221] Solvent: THF
[0222] Injection volume: 80μl
[0223] Measuring temperature: 40°C
[0224] Flow rate: 1ml / min
[0225] Detector: Differential refractometer.
[0226] (Measurement of IR spectrum)
[0227] The IR spectrum of the silane compound copolymer obtained in the manufacture example was measured using the following apparatus.
[0228] Fourier transfo...
manufacture example 1)
[0230] In a 300 ml eggplant-shaped flask, 16.7 g (84 mmol) of phenyltrimethoxysilane (manufactured by Tokyo Chemical Industry Co., Ltd.) as the silane compound (2) and 3-acetoxypropyltrimethoxysilane as the silane compound (1) were charged. 8.0 g (36 mmol) of methyl silane (manufactured by Aymax Co., Ltd.), 120 ml of toluene as a solvent, and 60 ml of distilled water, and then add 0.15 g (1.5 mmol) of phosphoric acid (manufactured by Kanto Chemical Co., Ltd.) as a catalyst while stirring, and continue stirring at room temperature 16 hours.
[0231] After completion of the reaction, 100 ml of ethyl acetate was added to the reaction mixture, and neutralized with saturated aqueous sodium bicarbonate solution. After standing still for a while, water was removed, and the organic layer was washed twice with distilled water, and dried over anhydrous magnesium sulfate. After filtering the magnesium sulfate, the filtrate was concentrated to 50 ml with a rotary evaporator, added dropwi...
manufacture example 2)
[0236] In Production Example 1, except that the usage-amount of phenyltrimethoxysilane was 14.3 g (72 mmol), and the usage-amount of 3-acetoxypropyltrimethoxysilane was 10.7 g (48 mmol). 1 was carried out in the same manner to obtain 15.9 g of a silane compound copolymer (A2).
[0237] The weight average molecular weight (Mw) of the silane compound copolymer (A2) was 2,600, and the molecular weight distribution (Mw / Mn) was 1.51.
[0238] In addition, the IR spectrum data of the silane compound copolymer (A2) are shown below.
[0239] Si-Ph: 699cm -1 , 741cm -1 , Si-O: 1132cm -1 ,-CO: 1738cm -1 .
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