Preparation method of high temperature-resistant boron carbide-silicon carbide compound aerogel
A technology of composite airgel and boron carbide, which is applied in the field of composite material preparation technology, can solve the problems of large volume of concrete materials, inability to use emergency and rapid use, poor neutron absorption effect, etc., and achieve low density, low thermal conductivity, high neutron Effect of Absorbing Sections
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Embodiment 1
[0025] Mix and stir 1 mol of resorcinol, 2 mol of formaldehyde, 15 mol of deionized water and 18 mol of absolute ethanol to obtain solution A. 0.1 mol of boric acid and 5 mol of absolute ethanol were ultrasonically mixed to obtain solution B. Add solution B and 1mol 3-aminopropyltriethylsilane to solution A and mix evenly to obtain a light yellow composite sol solution. Pour it into the mold, let it stand for 50 minutes, add absolute ethanol for solvent replacement, and replace it every 8 hours, and replace it 4 times in total. The replaced composite wet gel was subjected to CO 2 Supercritical drying treatment, in which the pressure of the kettle body is controlled at 12MPa, the temperature is controlled at 50°C, and the drying time is 8 hours to obtain a boron carbide-silicon carbide precursor. The obtained boron carbide-silicon carbide precursor was heated to 1500°C at a heating rate of 3°C / min under the protection of an argon atmosphere, and the holding time was 5 hours, ...
Embodiment 2
[0027] Mix and stir 1 mol of resorcinol, 2 mol of formaldehyde, 5 mol of deionized water and 26 mol of absolute ethanol to obtain solution A. 1.5 mol of boric acid and 8 mol of absolute ethanol were ultrasonically mixed to obtain solution B. Add solution B and 0.5mol 3-aminopropyltriethylsilane to solution A and mix evenly to obtain a pale yellow composite sol solution. Pour it into the mold, let it stand for 30 minutes, add absolute ethanol for solvent replacement, replace it every 12 hours, and replace it 3 times in total. The replaced composite wet gel was subjected to CO 2 Supercritical drying treatment, in which the pressure of the kettle body is controlled at 8MPa, the temperature is controlled at 60°C, and the drying time is 13 hours to obtain a boron carbide-silicon carbide precursor. The obtained boron carbide-silicon carbide precursor was heated to 1550°C at a heating rate of 2°C / min under the protection of a helium atmosphere, and the holding time was 6 hours, the...
Embodiment 3
[0029] Mix and stir 1 mol of resorcinol, 2 mol of formaldehyde, 10 mol of deionized water and 20 mol of absolute ethanol to obtain solution A. 2 mol of boric acid and 10 mol of absolute ethanol were ultrasonically mixed to obtain solution B. Add solution B and 1.5mol 3-aminopropyltriethylsilane into solution A, mix well and stir to obtain a pale yellow composite sol solution. Pour it into the mold, let it stand for 40 minutes, add absolute ethanol for solvent replacement, and replace it every 15 hours, and replace it 4 times in total. The replaced composite wet gel was subjected to CO 2 Supercritical drying treatment, in which the pressure of the kettle body is controlled at 11MPa, the temperature is controlled at 50°C, and the drying time is 12 hours to obtain a boron carbide-silicon carbide precursor. The obtained boron carbide-silicon carbide precursor was heated to 1450°C at a heating rate of 4°C / min under the protection of an argon atmosphere, and the holding time was 7...
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