Synthesis of Fine MoSi2–Si3N4 Composite Powders

IF 0.9 4区 材料科学 Q3 MATERIALS SCIENCE, CERAMICS
I. V. Kud, R. V. Lytvyn, L. A. Krushynska, O. M. Myslyvchenko, R. M. Mediukh, O. B. Zgalat-Lozynskyy
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Abstract

The features peculiar to the solid-state synthesis of MoSi2 through vacuum heat treatment of a powder mixture of molybdenum and silicon nitride, as a precursor, in the temperature range 1000–1400°C were examined. X-ray diffraction established that the solid-state interaction began at 1100°C and progressed through the reaction diffusion of highly active silicon, resulting from the decomposition of Si3N4, into molybdenum to form lower Mo3Si and Mo5Si3 silicide phases. In the temperature range 1100–1300°C, the redistribution of phases occurred: the contents of the starting molybdenum and β-Si3N4 components in the reaction mixtures gradually decreased, while the contents of lower molybdenum silicides increased. Molybdenum disilicide formed in situ at 1400°C via successive development of lower silicide phases. The final product contained Mo5Si3. This was attributed to a deficiency of silicon as it evaporated at a temperature above 1200°C. This led to the conclusion that the addition of 20 wt.% excess silicon nitride was necessary to produce a homogeneous MoSi2 phase and up to 40 wt.% excess silicon nitride to produce a two-phase MoSi2–Si3N4 composite powder. The elevated temperature in the synthesis of MoSi2 compared to conventional synthesis from simple elements was explained by the slow formation of active silicon in the Si3N4 dissociation process. Based on the features observed in the solid-state vacuum interaction within the powder mixture of molybdenum and silicon nitride, as a precursor, a method was proposed for producing MoSi2–Si3N4 composite powders, involving the introduction of 30 and 40 wt.% excess Si3N4 powder. The synthesis resulted in agglomerated composite powders with a homogeneous distribution of the MoSi2 and β -Si3N4 phases. The MoSi2 phase exhibited a capsular structure with a smooth surface. The synthesized composite powders are intended for the fabrication of components and parts with high oxidation resistance and corrosion resistance at elevated temperatures.

Abstract Image

Abstract Image

精细 MoSi2-Si3N4 复合粉末的合成
通过对作为前驱体的钼和氮化硅粉末混合物在 1000-1400°C 温度范围内进行真空热处理,研究了固态合成 MoSi2 的独特特征。X 射线衍射证实,固态相互作用从 1100°C 开始,通过 Si3N4 分解产生的高活性硅向钼的反应扩散,形成较低的 Mo3Si 和 Mo5Si3 硅化物相。在 1100-1300°C 的温度范围内,出现了相的重新分布:反应混合物中起始钼和β-Si3N4 成分的含量逐渐减少,而低钼硅化物的含量增加。通过低硅化物相的连续发展,二硅化钼在 1400°C 的温度下就地形成。最终产品含有 Mo5Si3。这归因于硅在 1200°C 以上的温度下蒸发时的不足。由此得出的结论是,要生成均匀的 MoSi2 相,必须添加 20 重量%的过量氮化硅,要生成 MoSi2-Si3N4 两相复合粉末,则必须添加多达 40 重量%的过量氮化硅。与传统的简单元素合成法相比,MoSi2 的合成温度较高,原因是 Si3N4 解离过程中活性硅的形成速度较慢。根据在作为前驱体的钼和氮化硅粉末混合物中观察到的固态真空相互作用特征,提出了一种生产 MoSi2-Si3N4 复合粉末的方法,包括引入 30 和 40 wt.% 的过量 Si3N4 粉末。合成结果是团聚的复合粉末,MoSi2 和 β -Si3N4 相分布均匀。MoSi2 相呈现出表面光滑的囊状结构。合成的复合粉末可用于制造在高温下具有高抗氧化性和耐腐蚀性的部件和零件。
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来源期刊
Powder Metallurgy and Metal Ceramics
Powder Metallurgy and Metal Ceramics 工程技术-材料科学:硅酸盐
CiteScore
1.90
自引率
20.00%
发文量
43
审稿时长
6-12 weeks
期刊介绍: Powder Metallurgy and Metal Ceramics covers topics of the theory, manufacturing technology, and properties of powder; technology of forming processes; the technology of sintering, heat treatment, and thermo-chemical treatment; properties of sintered materials; and testing methods.
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