镁热还原法制备硼化锆/硅化锆/氧化物复合粉体

Didem OVALI DÖNDAŞ
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引用次数: 0

摘要

本研究采用镁热还原法,以ZrO2、B2O3、Si和Mg为初始粉,研究了共合成硼化锆、硅化锆和氧化物粉末复合材料的方法。通过铣削时间、还原温度和过量镁的加入来考察高温陶瓷粉末的合成。用Factsage软件对可能的反应产物进行热化学分析。结果表明,热化学预测结果与所得粉末相具有良好的一致性。高能铣削对退火后硼化锆相的形成有显著影响。然而,从x射线衍射结果来看,延长磨矿时间和提高退火温度对复合粉末的组成没有显著影响。600℃的退火温度足以获得zrb2基陶瓷复合粉体。在最后的粉末相中,过量的镁加入到化学计量中显示出一个重要的特征。经磨矿、退火、浸出等工艺处理后的粉末化学计量成分为ZrB2、ZrSi、ZrSi2、ZrO2、MgSiO2,过量添加Mg的粉末结构为ZrB2、ZrSi、ZrSi2、ZrO2相。利用扫描电镜分析观察了合成过程中各个步骤粉末的形貌,揭示了合成粉末的精细结构形貌。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Co-synthesis of zirconium boride/silicide/oxide composite powders by magnesiothermic reduction
This study uses a magnesiothermic reduction method to investigate the co-synthesis of zirconium boride, silicides, and oxide powder composites using ZrO2, B2O3, Si, and Mg initial powders. The synthesis of high-temperature ceramic powders is examined through milling durations, reduction temperatures, and excess magnesium addition. Thermochemical analysis of probable reaction products was conducted by the Factsage software. According to the results, the thermochemical predictions and resultant powder phases showed good coherency. High-energy milling has a significant effect on the formation of the zirconium boride phase after annealing. However, extended milling time and higher annealing temperature have no significant effects on the composition of the constituted composite powders according to the X-ray diffraction results. An annealing temperature of 600 ºC was enough to obtain ZrB2-based ceramic composite powders. In the final powder phases, the excess magnesium addition to the stoichiometric displays an important feature. After the milling, annealing, and leaching procedure, the stoichiometric powder composition comprises ZrB2, ZrSi, ZrSi2, ZrO2, and MgSiO2, and excess Mg added powders have the ZrB2, ZrSi, ZrSi2, ZrO2 phases in their structure. Scanning electron microscopy analysis was utilized to observe the morphologies of the powders throughout each step of the synthesis procedure and revealed the finely structured morphology of synthesized powders.
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CiteScore
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