Method of synthesizing cubic boron nitride using alkali metal fluoride
A technology of alkali metal fluoride and cubic boron nitride, applied in chemical instruments and methods, nitrogen compounds, non-metallic elements, etc., can solve the problems of low conversion rate, achieve high crystal form integrity, improve conversion rate, and nucleate rate-enhancing effect
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Embodiment 1
[0013] Combine LiF, Li 3 N and LiH are mixed evenly in a weight ratio of 1:4:1, and then mixed with hexagonal boron nitride with a purity of 95% in a weight ratio of 15:85 and pre-pressed into a cylindrical shape and then loaded into a graphite sleeve to maintain the height of the raw material column It is equal to the height of the graphite tube or 0.5-1mm lower than the height of the graphite tube, put it into a pyrophyllite block to assemble a synthetic block, and perform high-pressure synthesis on a six-sided top press. Under the conditions of 1100°C and 4.5GPa, heat preservation and pressure for 5 minutes, stop heating and take out the sample after the temperature drops, and obtain red-yellow transparent cubic boron nitride crystals after acid-base purification treatment, and the obtained cBN crystals have high crystal form integrity. The conversion rate of cBN is 30-35%.
Embodiment 2
[0015] Combine LiF, Li 3 N and LiH are mixed evenly in a weight ratio of 4:5:1, and then mixed with hexagonal boron nitride with a purity of 95% in a weight ratio of 20:80 and pre-pressed into a cylindrical shape and then loaded into a graphite sleeve to maintain the height of the raw material column It is equal to the height of the graphite tube or 0.5-1mm lower than the height of the graphite tube, put it into a pyrophyllite block to assemble a synthetic block, and perform high-pressure synthesis on a six-sided top press. Under the conditions of 1700°C and 5.5GPa, heat preservation and pressure for 5 minutes, stop heating and take out the sample after the temperature drops, and obtain red-yellow transparent cubic boron nitride crystals after acid-base purification treatment. The obtained cBN crystals have high crystal form integrity , the conversion rate of cBN was 40%.
Embodiment 3
[0017] Sample proportioning, assembly, synthesis equipment, temperature and pressure conditions are all the same as in Example 1, and the heat preservation and pressure holding time is 3 minutes. The cBN crystal obtained after the experimental sample is purified is the same as in Example 1, only the particle size is slightly finer, and the cBN conversion rate is 30. %.
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