Method for preparing carbon fiber with boron nitride coating on surface from polyacrylonitrile
A technology of polyacrylonitrile and boron nitride, applied in the direction of fiber treatment, fiber type, fiber chemical characteristics, etc., can solve the problems of high cost, high coating process preparation temperature, complex process, etc., and achieves higher service temperature and higher temperature Antioxidant performance, solve the effect of complex process
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Embodiment 1
[0027] Step 1: Degreasing, decontaminating and drying the polyacrylonitrile surface;
[0028] Step 2: Using absolute ethanol as a solvent, dissolve boric acid and urea in absolute ethanol at a molar ratio of 2:1, configure the concentration of boric acid to be 0.6mol / L, stir and disperse it in an ultrasonic wave to a uniform solution, and then Put polyacrylonitrile into the solution and soak for 2h;
[0029] Step 3: Dry the modified polyacrylonitrile precursor obtained in step 2 in an oven at 80°C for 0.5h, then put the polyacrylonitrile precursor into a pre-oxidation furnace, heat it to 260°C, and pre-oxidize it in the air. Oxidation 2h;
[0030] Step 4: Put the modified polyacrylonitrile pre-oxidized wire obtained in Step 3 into a tube furnace, raise the temperature to 800°C at a rate of 2°C / min in a nitrogen atmosphere, then keep it warm for 4 hours, and then heat it up at a rate of 2°C / min. The samples were taken out after cooling down to room temperature.
[0031] The ...
Embodiment 2
[0033] Step 1: Degreasing, decontaminating and drying the polyacrylonitrile surface;
[0034] Step 2: Using absolute ethanol as a solvent, dissolve boric acid and urea in absolute ethanol at a molar ratio of 3:1, configure the concentration of boric acid to be 0.7mol / L, stir and disperse it in an ultrasonic wave to a uniform solution, and then Put polyacrylonitrile into the solution and soak for 2h;
[0035] Step 3: Dry the modified polyacrylonitrile precursor obtained in step 2 in an oven at 80°C for 0.5h, then put the polyacrylonitrile precursor into a pre-oxidation furnace, heat it to 260°C, and pre-oxidize it in the air. Oxidation 2.5h;
[0036] Step 4: Put the modified polyacrylonitrile pre-oxidized wire obtained in Step 3 into a tube furnace, raise the temperature to 800°C at a rate of 2°C / min in a nitrogen atmosphere, then keep it warm for 4 hours, and then heat it up at a rate of 2°C / min. The samples were taken out after cooling down to room temperature.
[0037] Th...
Embodiment 3
[0039] Step 1: Degreasing, decontaminating and drying the polyacrylonitrile surface;
[0040] Step 2: Using absolute ethanol as a solvent, dissolve boric acid and urea in absolute ethanol at a molar ratio of 3.5:1, configure the concentration of boric acid to be 0.6mol / L, stir and disperse it in an ultrasonic wave to a uniform solution, and then Put polyacrylonitrile into the solution and soak for 2h;
[0041] Step 3: Dry the modified polyacrylonitrile precursor obtained in step 2 in an oven at 80°C for 0.5h, then put the polyacrylonitrile precursor into a pre-oxidation furnace, heat it to 270°C, and pre-oxidize it in the air. Oxidation 2.5h;
[0042] Step 4: Put the modified polyacrylonitrile pre-oxidized wire obtained in Step 3 into a tube furnace, raise the temperature to 900°C at a rate of 3°C / min in a nitrogen atmosphere, then keep it warm for 5 hours, and then heat it at a rate of 3°C / min The samples were taken out after cooling down to room temperature.
[0043] The ...
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