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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 A degrees C for 4 h, formation of Si3N4 can be detected only when the C/SiO2 weight ratio is greater than similar to 2.0. The Si3N4 yield increases rapidly as the C/SiO2 weight ratio is increased from similar to 2.0 to 2.8 and decreases with further increase in the C/SiO2 ratio. The alpha-phase content increases with increasing C/SiO2 weight ratio and decreases with increasing temperature. Depending on the C/SiO2 ratio, a Si3N4 yield of similar to 80 wt% and an alpha-phase content of similar to 90 wt% could be obtained.
机译:通过使用固溶燃烧合成方法制备的前驱体粉末,研究了Si3N4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,其用作Si 3 N 4的碳热还原和氮化合成的前体粉末。在1,425-1,450 A的温度下进行碳热还原和氮化反应4小时时,只有当C / SiO2重量比大于2.0时,才能检测到Si3N4的形成。随着C / SiO2重量比从相似的2.0增加到2.8,Si3N4产率迅速增加,并且随着C / SiO2重量比的进一步增加而降低。 α相含量随C / SiO2重量比的增加而增加,随温度的升高而减少。取决于C / SiO 2的比率,可以获得类似于80wt%的Si 3 N 4产率和类似于90wt%的α相含量。

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