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Carbothermal reduction and nitridation synthesis of silicon nitride by using solution combustion synthesized precursors

机译:固溶燃烧合成前驱体碳热还原氮化合成氮化硅

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Carbothermal reduction and nitridation synthesis of Si3N4 was investigated by using precursor powders prepared by a solution combustion synthesis method. Glycine or urea (fuel), ammonium nitrate (oxidizer), silicic acid (Si source), and sucrose (major carbon source) were dissolved completely in water. This solution was dried and then heated to undergo the solution combustion synthesis reaction, resulting in a homogeneous mixture of nano-sized carbon and SiO2 particles, which was used as the precursor powder for the carbothermal reduction and nitridation synthesis of Si3N4. When the carbothermal reduction and nitridation reaction was carried out at 1,425–1,450 °C for 4 h, formation of Si3N4 can be detected only when the C/SiO2 weight ratio is greater than ~2.0. The Si3N4 yield increases rapidly as the C/SiO2 weight ratio is increased from ~2.0 to 2.8 and decreases with further increase in the C/SiO2 ratio. The α-phase content increases with increasing C/SiO2 weight ratio and decreases with increasing temperature. Depending on the C/SiO2 ratio, a Si3N4 yield of ~80 wt% and an α-phase content of ~90 wt% could be obtained.
机译:利用溶液燃烧合成法制备的前驱体粉末,研究了Si 3 N 4 的碳热还原和氮化合成。甘氨酸或尿素(燃料),硝酸铵(氧化剂),硅酸(硅源)和蔗糖(主要碳源)完全溶解在水中。将该溶液干燥,然后加热以进行溶液燃烧合成反应,得到纳米级碳和SiO 2 颗粒的均匀混合物,用作碳热还原和氮化的前体粉末。 Si 3 N 4 的合成在1,425–1,450°C下进行碳热还原和氮化反应4 h时,只有在C / SiO <3时才能检测到Si 3 N 4 的形成。 sub> 2 的重量比大于〜2.0。随着C / SiO 2 的重量比从〜2.0增加到2.8,Si 3 N 4 的产率迅速增加,并且随着C / SiO 2 的重量比的降低而降低C / SiO 2 比。 α相含量随C / SiO 2 重量比的增加而增加,随温度的升高而降低。取决于C / SiO 2 的比率,Si 3 N 4 的收率为〜80 wt%,α相含量为〜90可以得到wt%。

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