Polyurethane resin composition for sealing optoelectric conversion devices
A technology of polyurethane resin and resin composition, which is applied in the field of polyurethane resin, and can solve problems such as poor weather resistance stability and blackening of silver parts
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preparation Embodiment 1
[0235] Preparation Example 1 (Synthesis of Polyol A)
[0236] 680.2 g of pentaerythritol and 86.23 g of potassium hydroxide were added to a pressure vessel (hereinafter referred to as an autoclave) under a nitrogen atmosphere equipped with a stirrer, a temperature controller, a barometer, a nitrogen introduction tube, and a monomer introduction tube. . The autoclave was then replaced with nitrogen at room temperature, thereby reducing the internal pressure to 6.55 kPa. Then 897.3 g of propylene oxide was added in one portion, and the mixture was gradually heated to 115° C. with stirring, at which temperature the reaction was continued until no change in autoclave pressure was observed. Then, the pressure of the autoclave was lowered at the same temperature and kept at 665 Pa for 30 minutes to recover unreacted propylene oxide, and thus, crude polyol A was obtained.
[0237] Then, the crude polyol A was added to a separable flask (hereinafter referred to as "separable flask")...
preparation Embodiment 2
[0239] Preparation Example 2 [Synthesis of Polyurethane Prepolymer Terminated with Isocyanate Group (A-1)]
[0240] Mix 893.4g of "'COSMONATE' (registered trade name) NBDI" (2,5-diisocyanatomethylbicyclo[2.2.1]heptane and 2,6-diisocyanatomethylbicyclo[2.2.1]heptane A mixture of cyclo[2.2.1]heptane, produced by Mitsui Chemicals, Inc., hereinafter referred to as "NBDI") was added to a 1-liter separable flask equipped with a stirrer which had been dried and replaced with nitrogen, and 106.6 g Polyol A obtained in Preparation Example 1. Under the protection of nitrogen flow, the mixture was reacted at 100° C. for 8 hours, and then stored at room temperature for one day. Therefore, an isocyanate group-terminated polyurethane prepolymer (A-1) with an NCO% of 30.0 was obtained.
preparation Embodiment 3
[0241] Preparation Example 3 [Synthesis of isocyanate group-terminated polyurethane prepolymer (A-2)]
[0242] 833.6 g of NBDI was charged into the same apparatus as in the above preparation of the isocyanate group-terminated polyurethane prepolymer of Preparation Example 1, and 166.4 g of Polyol A obtained in Preparation Example 1 was added thereto. Under the protection of nitrogen flow, the mixture was reacted at 100° C. for 8 hours, and then stored at room temperature for one day. Therefore, an isocyanate group-terminated polyurethane prepolymer (A-2) with an NCO% of 24.0 was obtained.
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