Polycarbonate diol composition
A polycarbonate diol, polycarbonate technology, used in polyurea/polyurethane coatings, coatings, textiles and papermaking, etc., can solve the problems of heat resistance, poor weather resistance, poor hydrolysis resistance, etc., and achieve film-forming properties. Excellent effect, excellent low temperature flexibility, excellent oleic acid resistance and heat and humidity resistance
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[0211] Hereinafter, the present embodiment will be described more specifically with reference to specific examples and comparative examples, but the present embodiment is not limited to these examples and comparative examples at all unless the gist of the present embodiment is exceeded. In this example, unless otherwise stated, "parts" and "%" are based on mass standards.
[0212] The physical properties and evaluations in Examples and Comparative Examples described later were measured and evaluated by the methods shown below.
[0213] [Property 1] Hydroxyl Value
[0214] The hydroxyl value of polycarbonate diol (composition) is measured by the following method.
[0215]First, using a volumetric flask, pyridine was added to 12.5 g of acetic anhydride to prepare 50 mL, and an acetylating reagent was prepared. Next, 2.5 g of the sample was precisely weighed into a 100 mL eggplant-shaped flask. Next, 5 mL of the acetylation reagent and 10 mL of toluene were added to the eggpla...
Synthetic example 1
[0268] [Synthesis example 1] Production of polycarbonate diol P-1
[0269] 230 g of 1,5-pentanediol, 250 g of 1,6-hexanediol, and carbonic acid were put into a 1-L glass flask (hereinafter also referred to as "reactor") equipped with a rectification column filled with regular packing and a stirring device. After 400 g of ethylene ester, 0.0468 g of titanium tetra-n-butoxide was added as a catalyst. The reactor was immersed in an oil bath at 180°C, and the reaction was performed at a reaction temperature of 165°C for 12 hours while extracting a part of the distillate. Next, the reactor was directly connected to the condenser, the temperature of the oil bath was raised to 180° C., the pressure was gradually lowered, and the reaction was further carried out for 3 hours to obtain polycarbonate diol P-1 that was liquid at room temperature (466g). The hydroxyl value of the obtained polycarbonate diol P-1 was 55.2 mgKOH / g. In addition, the number average molecular weight of the ob...
Synthetic example 2
[0270] [Synthesis example 2] Production of polycarbonate diol P-2
[0271] 270 g of 1,6-hexanediol, 250 g of 1,4-butanediol and After 445 g of ethylene carbonate, 0.0960 g of titanium tetra-n-butoxide was charged as a catalyst. The reactor was immersed in an oil bath at 140 to 160°C, and a part of the distillate was extracted, and the reaction was performed at a reaction temperature of 90 to 160°C for 20 hours. Next, the reactor was directly connected to the condenser, the temperature of the oil bath was raised to 180° C., the pressure was gradually lowered, and the reaction was further carried out for 8 hours to obtain a polycarbonate diol P- 2 (462 g). The hydroxyl value of the obtained polycarbonate diol P-2 was 55.8 mgKOH / g. In addition, the number average molecular weight of the obtained polycarbonate diol P-2 was 2010.
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