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Alumina-Doped Zirconia Submicro-Particles: Synthesis Thermal Stability and Microstructural Characterization

机译:氧化铝掺杂的氧化锆亚微颗粒:合成热稳定性和微结构表征

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摘要

Zirconia nanoceramics are interesting materials for numerous high-temperature applications. Because their beneficial properties are mainly governed by the crystal and microstructure, it is essential to understand and control these features. The use of co-stabilizing agents in the sol-gel synthesis of zirconia submicro-particles should provide an effective tool for adjusting the particles’ size and shape. Furthermore, alumina-doping is expected to enhance the particles’ size and shape persistence at high temperatures, similar to what is observed in corresponding bulk ceramics. Dispersed alumina should inhibit grain growth by forming diffusion barriers, additionally impeding the martensitic phase transformation in zirconia grains. Here, alumina-doped zirconia particles with sphere-like shape and average diameters of 300 nm were synthesized using a modified sol-gel route employing icosanoic acid and hydroxypropyl cellulose as stabilizing agents. The particles were annealed at temperatures between 800 and 1200 C and characterized by electron microscopy, elemental analysis, and X-ray diffraction. Complementary elemental analyses confirmed the precise control over the alumina content (0–50 mol%) in the final product. Annealed alumina-doped particles showed more pronounced shape persistence after annealing at 1000 C than undoped particles. Quantitative phase analyses revealed an increased stabilization of the tetragonal/cubic zirconia phase and a reduced grain growth with increasing alumina content. Elemental mapping indicated pronounced alumina segregation near the grain boundaries during annealing.
机译:氧化锆纳米陶瓷是用于许多高温应用的有趣材料。由于它们的有益特性主要取决于晶体和微结构,因此了解和控制这些特性至关重要。在氧化锆亚微粒的溶胶-凝胶合成中使用助稳定剂应该为调节微粒的大小和形状提供有效的工具。此外,与在相应的块状陶瓷中观察到的情况相似,氧化铝的掺杂有望提高颗粒的尺寸和高温下的形状持久性。分散的氧化铝应通过形成扩散壁垒来抑制晶粒的生长,另外还阻碍了氧化锆晶粒中的马氏体相变。在这里,氧化铝掺杂的氧化锆颗粒呈球形,平均直径为 300 n m 使用二十烷酸和羟丙基纤维素,通过改进的溶胶-凝胶途径合成作为稳定剂。粒子在800到1200之间的温度下退火。 C ,并通过电子显微镜,元素分析进行​​表征和X射线衍射。补充元素分析证实了对最终产品中氧化铝含量(0–50 mol%)的精确控制。退火氧化铝掺杂颗粒在1000 < msup> C 比未掺杂的粒子好。定量相分析表明,随着氧化铝含量的增加,四方/立方氧化锆相的稳定性增强,晶粒生长减少。元素映射表明在退火过程中靠近晶界的氧化铝明显偏析。

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