Method for preparing hexagonal boron nitride coating on surface of carbon fiber material
A technology of hexagonal boron nitride and carbon fiber, which is applied in the fields of carbon fiber, fiber treatment, textiles and papermaking, etc., can solve the problems of biological toxicity, high surface tension, and easy methanol volatilization, and achieve good electrical insulation properties, control coating The effect of simple layer thickness and preparation process
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Embodiment 1
[0027] Such as figure 1 Shown, the preparation method of the present embodiment comprises the following steps:
[0028] Step 1. Carbon fiber surface pretreatment: put the carbon fiber in acetone for 36 hours to remove the epoxy organic matter on the surface of the carbon fiber, then ultrasonically treat it for 20 minutes to fully disperse the carbon fiber fibroin into monofilaments, and then wash it with distilled water for 3 times Then place it in a vacuum drying oven at 60°C for 8 hours, and finally place it in a muffle furnace at 300°C for surface activation treatment on the carbon fiber for 25 minutes;
[0029] Step 2. Precursor preparation: use boric acid as the boron source of the hexagonal boron nitride coating, and urea as the nitrogen source of the hexagonal boron nitride coating. The mass ratio of the boric acid and urea is 1:2, and the boric acid and urea are mixed After uniformity, heat and melt in a vacuum drying oven at a temperature of 180°C, and stir for 10 mi...
Embodiment 2
[0036] Such as figure 1 Shown, the preparation method of the present embodiment comprises the following steps:
[0037] Step 1. Carbon fiber surface pretreatment: put the carbon fiber in acetone for 24 hours to remove the epoxy organic matter on the surface of the carbon fiber, then ultrasonically treat it for 30 minutes to fully disperse the carbon fiber fibroin into monofilaments, and then wash it 4 times with distilled water Then place it in a vacuum drying oven at 70°C for 12 hours, and finally place it in a muffle furnace at 350°C for surface activation treatment on the carbon fiber for 20 minutes;
[0038] Step 2. Precursor preparation: use boric acid as the boron source of the hexagonal boron nitride coating, and urea as the nitrogen source of the coating. The mass ratio of the boric acid and urea is 1:2. Mix the boric acid and urea evenly and place Heat and melt in a vacuum drying oven at a temperature of 170°C, and stir for 20 minutes to obtain a uniform liquid precu...
Embodiment 3
[0045] Such as figure 1 Shown, the preparation method of the present embodiment comprises the following steps:
[0046] Step 1. Carbon fiber surface pretreatment: put the carbon fiber in acetone for 48 hours to remove the epoxy organic matter on the surface of the carbon fiber, then ultrasonically treat it for 30 minutes to fully disperse the carbon fiber fibroin into monofilaments, and then wash it with distilled water for 4 times Then place it in a vacuum drying oven at 70°C for 12 hours, and finally place it in a muffle furnace at 350°C for surface activation treatment on the carbon fiber for 30 minutes;
[0047] Step 2. Precursor preparation: use boric acid as the boron source of the hexagonal boron nitride coating, and urea as the nitrogen source of the coating. The mass ratio of the boric acid and urea is 1:3. Mix the boric acid and urea evenly and place Heat and melt in a vacuum drying oven at a temperature of 160°C, and stir for 30 minutes to obtain a uniform liquid p...
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