氧化锆纳米粉体压实过程中高压对材料结构形成的影响

S. Porozova, L. Sirotenko, V. O. Shokov
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引用次数: 0

摘要

研究了在钢模中半干压氧化锆纳米粉(部分氧化钇稳定)过程中的压实压力对压坯和样品在1400℃烧结2小时的相组成和显微组织的影响。聚乙烯醇水溶液作为临时工艺粘合剂。通过x射线荧光分析,溶胶-凝胶法(相应试剂的水-乙醇溶液与琼脂添加剂用氨水沉淀)合成的粉末中钇的含量为3.2 mol.%。本文提供了用拉曼光谱、光学显微镜和原子力显微镜对压坯和烧结样品进行研究的结果。发现它们的密度增加不是一个单调的过程。在Р = 400÷450 MPa的临界压实压力区间内,材料孔隙率、孔隙形状和大小、微观结构和相组成发生急剧变化。在压实样品中观察到单斜相与四方氧化锆。其内容随Р值的变化而变化。物料颗粒的磨碎与团聚体破坏过程相关联,在Р = 350÷550 MPa区间内主动发生。其他研究人员在氧化锆纳米粉压紧过程中观察到类似的效果,他们认为纳米粉系统对压力影响的响应与对水成分的影响有关(在这种情况下,是临时工艺粘合剂),并且是由于在10-25°С和400-700 MPa下一种水形态向另一种水形态的转变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of high pressures during compaction of zirconia nanopowder on material structure formation
The study covers the effect of compaction pressure during semi-dry pressing of zirconia nanopowder partially stabilized with yttria in a steel mold on the phase composition and microstructure of compacts and samples sintered at 1400 °C for 2 hours. An aqueous solution of polyvinyl alcohol was used as a temporary process binder. According to X-ray fluorescence analysis, the content of yttria in the powder synthesized by sol-gel technology (precipitation with aqueous ammonia solution from water-ethanol solutions of the corresponding reagents with the agar-agar additive) was 3.2 mol.%. The paper provides the results obtained when studying compacts and sintered samples by Raman spectroscopy, optical and atomic force microscopy. It was found that the increase in their density is not a monotonous process. There is a critical compaction pressure interval of Р = 400÷450 MPa where a sharp change in the material porosity, pore shape and size, microstructure and phase composition occurs. A monoclinic phase was observed in compacted samples along with tetragonal zirconia. Its content varies with a variation in Р values. The grinding of material grains is associated with the agglomerate destruction process and actively occurs in the interval of Р = 350÷550 MPa. A similar effect was observed by other researchers during zirconia nanopowder compaction who suggested that the nanopowder system response to the effect of pressure is related to the influence on the water component (in this case, the temporary process binder) and is due to the transition of one water form to another at 10–25 °С and 400–700 MPa.
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