Polyurethane elastomer
A technology of polyurethane elastomer and prepolymer, applied in the field of polyurethane elastomer, can solve problems such as difficulty in meeting the requirements of special fields, and achieve the effect of simple preparation process
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Embodiment 1
[0023] Example 1 Preparation of polyether polyols:
[0024] The polyether polyol in the present invention is obtained by adopting known ionic ring-opening polymerization method, and the specific method is: add 1,2-propylene glycol, potassium hydroxide 0.2% (based on the total amount of feed, potassium hydroxide The amount of addition is 0.2% of the total weight of 1,2-propylene glycol, propylene oxide and ethylene oxide), nitrogen replacement 3 times, then vacuumize, heat up to 80 ℃, and then slowly add propylene oxide and ethylene oxide Alkanes, the reaction pressure is kept below 0.44 MPa, the reaction temperature is controlled at 115 ± 2 ℃, after 4 hours of reaction, the temperature is lowered to 80-90 ℃, and the hydroxyl value is measured by sampling to obtain crude polyether. After measuring its hydroxyl value in the range of 55-57KOHmg / g, add an appropriate amount of pure water, 1.2% phosphoric acid, and 0.5% magnesium silicate (based on the total feeding amount) into t...
Embodiment 2
[0027] Example 2 Preparation of polyester polyol :
[0028] The polyester polyol among the present invention adopts known polycondensation method to obtain, and the method that adopts is vacuum dehydration method. Weigh adipic acid, diethylene glycol and dipropylene glycol according to the ratio shown in Table 2, put the above-mentioned substances into the reaction kettle, first pass nitrogen gas for 10 min, remove the air in the system, and then protect it under nitrogen protection. Under heating and stirring, after the material is melted, 0.1% of the total weight of the material is added as a catalyst tetrabutyl titanate. Water begins to flow out at about 140°C, continue heating, and the theoretical water will finish when the temperature in the reactor reaches about 220°C. Keep warm for 2 hours after the water comes out, then stop the nitrogen flow. Start vacuuming step by step, the vacuum degree is 20 kPa, 1 h; 13.2 kPa, 1 h; 6.7 kPa, 1 h, sampling and analyzing acid. ...
Embodiment 3
[0033] The invention adopts the known prepolymer method to prepare the polyurethane elastomer, that is, first prepares the isocyanate prepolymer, and then performs chain extension to obtain the polyurethane elastomer.
[0034] The first step: dehydrate the complex polyol (the polyether polyol and polyester polyol prepared in Examples 1 and 2 in the ratio shown in Table 3) at 1 0 0 ~ 1 3 0 ℃ for 2 ~ 3 hours in vacuum dehydration, and then Cool to 50-60°C, quickly add liquid diisocyanate (2-5 times the molar weight of the complex polyol, see Table 3) under rapid stirring, after 30-40 min, at 80-85°C Insulate and react for 2 to 3 hours, take samples to analyze the content of free isocyanate groups, then vacuum defoam for 20 to 30 min, and seal and store for later use.
[0035] Step 2: Weigh 80-100g of isocyanic acid prepolymer, stir and heat up to 80-85°C, vacuum defoaming for 1-2 minutes, add a chain extender equivalent to NCO under rapid stirring MOCA, after stirring for about...
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Abstract
Description
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