温度和升温速率模式对氧化铝微观组织和力学性能的影响:放电等离子烧结机理分析

M. Boldin, A. Popov, А. Nokhrin, V. Chuvil’deev, A. Murashov, G. V. Sherbak, N. Tabachkova
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摘要

研究了温度和升温速率对亚微米和细分散氧化铝粉体收缩动力学的影响。研究对象为(1)亚微米级α-Al2O3粉末;(2)颗粒表面有非晶层的亚微米级α-Al2O3粉末;(3)细粒级α-Al2O3粉末。采用火花等离子烧结(SPS)法制备陶瓷样品。通过对相同分散度粉末(1)和(2)的比较,分析了非晶层对烧结动力学的影响。通过对粉体(1)和粉体(3)的对比,分析了初始粒径对收缩动力学的影响。收缩曲线分析采用Young-Cutler模型和Coble模型。结果表明,亚微米粉体的烧结动力学由晶界扩散过程的强度决定,细粒粉体的烧结动力学由体积扩散和晶界扩散过程同时进行决定。结果表明,亚微米级α-Al2O3粉末表面非晶层的存在影响了SPS最后阶段的晶界速率和Coble方程参数。结果表明,表面有非晶层的亚微米粉末陶瓷SPSed的异常特性与非晶层结晶过程中晶界上缺陷密度增大和自由体积过大有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of the temperature and heating rate modes on the microstructure and mechanical properties of aluminum oxide: analysis of Spark Plasma Sintering mechanisms
The effect of temperature and heating rate on the shrinkage kinetics of submicron and fine-dispersed aluminum oxide powders was investigated. The objects of the study were (1) submicron powder α-Al2O3, (2) submicron powder α-Al2O3 with an amorphous layer on the particle surface, (3) fine powder α-Al2O3. Ceramic samples were obtained by spark plasma sintering (SPS). Based on a comparison of powders (1) and (2) of the same dispersity the influence of the amorphous layer on the sintering kinetics was analyzed. Based on the comparison of powders (1) and (3) the effect of the initial particle size on the shrinkage kinetics was analyzed. Shrinkage curves were analyzed using the Young-Cutler model and the Coble model. It is shown that the sintering kinetics of submicron powders is determined by the intensity of the grain boundary diffusion process, and of fine powders by simultaneously proceeding processes of volume and grain boundary diffusion. It was found that the presence of an amorphous layer on the surface of submicron α-Al2O3 powder influences the grain boundary rate and the parameters of the Coble equation at the final stage of SPS. It was suggested that the abnormal characteristics of ceramics SPSed from submicron powder with an surface amorphous layer are related to the presence of an increased density of defects and excess free volume on the grain boundaries formed in the process of crystallization of the amorphous layer.
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