Phase separation, crystallization and polyamorphism in the Y2O3-Al2O3 system

被引:45
作者
Skinner, Lawrie B. [1 ]
Barnes, Adrian C. [1 ]
Salmon, Philip S. [2 ]
Crichton, Wilson A. [3 ]
机构
[1] Univ Bristol, HH Wills Phys Lab, Royal Ft, Bristol BS8 1TL, Avon, England
[2] Univ Bath, Dept Phys, Bath BA2 7AY, Avon, England
[3] European Synchrotron Radiat Facil, F-38043 Grenoble, France
基金
英国工程与自然科学研究理事会;
关键词
D O I
10.1088/0953-8984/20/20/205103
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
A detailed study of glass formation from aerodynamically levitated liquids in the (Y2O3) x (Al2O3)(1-x) system for the composition range 0.21 <= x <= 0.41 was undertaken by using pyrometric, optical imaging and x-ray diffraction methods. Homogeneous and clear single-phase glasses were produced over the composition range 0.27 less than or similar to x less than or similar to 0.33. For Y2O3-rich compositions (0.33 <= x <= 0.375), cloudy materials were produced which contain inclusions of crystalline yttrium aluminium garnet (YAG) of diameter up to 40 mu m in a glassy matrix. For Y2O3-poor compositions around x = 0.24, cloudy materials were also produced, but it was not possible to deduce whether this resulted from (i) sub-micron inclusions of a nano-crystalline or glassy material in a glassy matrix or (ii) a glass formed by spinodal decomposition. For x = 0.21, however, the sample cloudiness results from crystallization into at least two phases comprising yttrium aluminium perovskite and alumina. The associated pyrometric cooling curve shows slow recalescence events with a continuous and slow evolution of excess heat which contrasts with the sharp recalescence events observed for the crystallization of YAG at compositions near x = 0.375. The materials that are the most likely candidates for demonstrating homogeneous nucleation of a second liquid phase occur around x = 0.25, which corresponds to the limit for formation of a continuous random network of corner-shared AlO4 tetrahedra.
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页数:9
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