离子半径
材料科学
镧系元素
三元运算
钇
立方氧化锆
氧化物
铈
相图
哈夫尼亚
相(物质)
离子键合
热力学
固溶体
物理化学
陶瓷
无机化学
离子
冶金
化学
程序设计语言
有机化学
物理
计算机科学
标识
DOI:10.1016/j.jeurceramsoc.2008.01.009
摘要
Abstract The systematic study of phase equilibria in the ternary systems HfO2(ZrO2)–Y2O3–Ln2O3 has been first carried out. Phase reactions and crystallization of ceramic alloys in the binary systems ZrO2–Ln2O3, HfO2–Ln2O3, Y2O3–Ln2O3 and phase equilibria in the series of ternary systems HfO2–Y2O3–Ln2O3 and ZrO2–Y2O3–Ln2O3 have been developed at high temperature. The most general regularities of the phase reactions in liquid and solid states inherent in these systems have been considered dependent on lanthanide ion radii. Taking into account literature data and newly developed results in binary and ternary systems, the analysis of the main regularities revealed in the constitution of phase diagrams, particularly its dependence on lanthanide ionic radius, was carried out. It was shown that temperature and composition of eutectic reaction, temperature of the pyrochlore phase decomposition, lattice parameters of solid solutions and other parameters of the binary phases linearly depend on ionic radius of lanthanide. For the first time it has been found that the affiliation of lanthanide oxides to cerium or yttrium subgroups predetermines phase relations in the systems and topology of the ternary phase diagrams. The data obtained are the basis for the novel prospective ceramic materials for both structural and functional applications in energetic, medicine, nuclear industry, thermal barrier coatings, solid oxide fuel cells, etc.
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