Method for synthesizing cubic boron nitride by using Mg3N2 and CaH2
A technology of cubic boron nitride and hexagonal boron nitride, which is applied in chemical instruments and methods, nitrogen compounds, and ultra-high pressure application processes, etc., can solve problems such as low conversion rate, achieve high conversion rate, and be beneficial to industrial production. , the effect of low purity requirements
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Embodiment 1
[0012] Raw materials choose Mg by weight ratio 3 N 2 : CaH 2 : hexagonal boron nitride = 7.5: 7.5: 85. Mg 3 N 2 and CaH 2 Mix evenly, then mix evenly with hexagonal boron nitride with a purity of 90% and pre-press it into a cylindrical shape, then put it into a graphite sleeve, keep the height of the raw material column equal to the height of the graphite tube or 0.5-1mm lower than the height of the graphite tube, Put it inside a pyrophyllite block to assemble into a crafting block. After preheating in an oven with a set temperature of 100° C. for 20 minutes, high-pressure synthesis was carried out on a six-sided top press. Under the conditions of temperature 1050°C and pressure 4.5GPa, heat preservation and pressure for 5 minutes, stop heating and take out the sample after the temperature drops. After acid-base purification treatment, yellow translucent cubic boron nitride crystals are obtained. The obtained cBN crystal has a higher crystal form integrity rate, and th...
Embodiment 2
[0014] Raw material ratio, assembly method, synthesis equipment, temperature, and pressure conditions are the same as in Example 1, and the heat preservation and pressure holding time is 3 minutes. The cBN crystal obtained after the sample is purified is the same as in Example 1, and the crystal particle size is slightly finer than that of Example 1. , cBN conversion rate 30 ~ 35%.
Embodiment 3
[0016] Raw material ratio, assembly mode, synthetic equipment and temperature, pressure condition are all the same as embodiment 1, and the heat preservation and pressure holding time is 8 minutes, and the cBN crystal obtained after the sample is purified is the same as embodiment 1, and the crystal particle size is thicker than embodiment 1 ( Granularity≥100 # accounted for about 50%), the crystal form integrity rate is high, and the cBN conversion rate is 40%.
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