Method for preparing polyacrylonitrile based carbon fibre spinning solution
A polyacrylonitrile-based carbon and fiber spinning technology, which is applied in the fields of fiber chemical characteristics, textiles and papermaking, etc., to achieve the effects of reducing residual initiator content, improving PAN purity, and simple process
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Embodiment 1
[0009] Example 1: (1) Weigh 600 grams of purified acrylonitrile, 6000 grams of dimethylformamide, 6 grams of water, 12 grams of acetic acid, add 3 grams of azobisisobutyronitrile, under nitrogen protection at 70 ° C React for 1 hour. (2) Pass ammonia gas through the system to make PH = 9, and terminate the polymerization reaction. (3) Continue to pass ammonia gas to adjust the pH to 11, raise the system temperature to 95° C., hydrolyze for 40 minutes, remove the single and defoam, and obtain the spinning solution.
Embodiment 2
[0010] Embodiment 2: (1) take by weighing 400 grams of purified acrylonitrile, 800 grams of dimethylformamide, 40 grams of water, 2 grams of formic acid, add 1 gram of azobisisobutyronitrile, under nitrogen protection at 50 °C for 15 hours. (2) Feed ammonia gas into the system to make PH = 8, and terminate the polymerization reaction. (3) Continue to pass ammonia gas to adjust the pH to 14, raise the system temperature to 100° C., hydrolyze for 5 minutes, remove single and defoam, and obtain a spinning solution.
Embodiment 3
[0011] Embodiment 3: (1) take by weighing 1000 grams of purified acrylonitrile, 3600 grams of dimethylformamide, 20 grams of water, 20 grams of formamide, add 5 grams of azobisisobutyronitrile, under nitrogen protection React at 60°C for 8 hours. (2) Feed ammonia gas into the system to make PH=9, and the polymerization reaction is terminated. (3) Maintain the pH at 9, raise the temperature of the system to 80° C., hydrolyze for 2 hours, remove the single and defoam, and obtain the spinning solution.
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