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Nanostructural study of sol-gel-derived zirconium oxides

机译:溶胶凝胶衍生的氧化锆的纳米结构研究

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Two sol-gel derived zirconia powders were prepared at pH = 0.5 and pH = 5.5. They were investigated as a function of temperature using mainly perturbed angular correlation spectroscopy. The aim was to elucidate the relationship between the nanoscopic configurations around Zr~(4+) ions and the morphology and structure of the powders. The highly porous material resulting from the solution at higher pH could be described mainly by defective and disordered, very hydrolyzed tetragonal arrays. As temperature increased, the amount of these arrays decreased while they became increasingly asymmetric, thus suggesting their superficial localization. The easy removal of hydroxyls led to the early appearance of the monoclinic phase. The gel obtained from the precursor at pH = 0.5 was entirely described by configurations still involving organic residues. After their calcination, the powder underwent a well-defined two-step hydroxyl removal thermal process leading to the crystallization of the tetragonal and the monoclinic phases. The thermal stability of the metastable tetragonal phase in the investigated powders seems to be controlled by their different capability to absorb oxygen.
机译:在pH = 0.5和pH = 5.5下制备了两种溶胶-凝胶衍生的氧化锆粉末。主要使用摄动角相关光谱法研究了它们与温度的关系。目的是阐明Zr〜(4+)离子周围的纳米结构与粉末的形态和结构之间的关系。由较高pH值的溶液产生的高度多孔的材料主要可以描述为有缺陷和无序,水解程度很高的四边形阵列。随着温度升高,这些阵列的数量减少,而它们变得越来越不对称,从而表明它们的表面定位。羟基的容易去除导致单斜相的早期出现。在pH = 0.5时从前体获得的凝胶完全由仍涉及有机残留物的构型描述。煅烧后,粉末经过明确定义的两步羟基去除热过程,导致四方相和单斜晶相结晶。在研究的粉末中,亚稳态四方相的热稳定性似乎受其吸收氧气的能力不同所控制。

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