Preparation method of chlorine-resistant black polyurethane urea elastic fiber
A polyurethane urea and elastic fiber technology, applied in the field of chlorine-resistant black polyurethane urea elastic fiber, can solve the problems of low cleaning fastness, poor color fastness of dark color, dyeing, etc., and achieves strength retention rate and elastic recovery Excellent strength, excellent strength retention, excellent elastic recovery rate
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[0021] One embodiment of the present invention is a preparation method of chlorine-resistant black polyurethane urea elastic fiber, the above-mentioned chlorine-resistant black polyurethane urea elastic fiber contains carbon black, and the preparation method of chlorine-resistant black polyurethane urea elastic fiber comprises: preparing polyurethane urea polymer The step of: mixing the slurry composition comprising the anti-chlorine agent, carbon black and polyurethane prepolymer with unreacted terminal isocyanate groups in the above polyurethane urea polymer to prepare the spinning stock solution; and using the above spinning stock solution to carry out The steps of spinning.
[0022] In one embodiment of the present invention, the polyurethane prepolymer may include 2.4 mol % to 3.5 mol % of unreacted terminal isocyanate groups. In one embodiment of the present invention, the above-mentioned polyurethane urea polymer can be prepared by the following steps: adding polytetram...
Embodiment 1
[0101] 1) Use a quantitative pump to continuously transfer 155.43 g / min of polytetramethylene ether glycol (molecular weight: 1800) and 36.71 g / min of diphenylmethane-4,4 to a 40° C. uniform mixer (Static Mixer). '-diisocyanate and mixed, put into a continuous polymerization tube in the form of a cylindrical tube at 80°C, and reacted for 135 minutes. By adjusting the reaction, the unreacted diisocyanate at the end was 2.64±0.02 mole percent, and synthesized as the first polymerization Polyurethane prepolymers.
[0102] Cool the above-mentioned first polymer to 40°C and stabilize it for 24 hours. Before putting it into the second reactor, put it into the high-end mixer continuously with 309.93 g / min of N,N-dimethylacetamide at 3500 rpm Stir vigorously for 20 seconds. The above-mentioned primary polymer was completely dissolved, and a 40°C polyurethane polymer solution having a solids content of 38.27% by weight was prepared by cooling.
[0103] 2) Prepared 4.955kg of ethylene...
Embodiment 2
[0110] In Example 1, except that the reaction was adjusted so that the unreacted diisocyanate at the end was 2.24±0.02 mole percent to prepare the polyurethane prepolymer as the first polymer, it was carried out in the same manner.
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