MARTENSITIC TOUGHENING OF CERAMICS

被引:44
作者
KRIVEN, WM [1 ]
机构
[1] UNIV ILLINOIS,MAT RES LAB,URBANA,IL 61801
来源
MATERIALS SCIENCE AND ENGINEERING A-STRUCTURAL MATERIALS PROPERTIES MICROSTRUCTURE AND PROCESSING | 1990年 / 127卷 / 02期
关键词
D O I
10.1016/0921-5093(90)90316-U
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Current knowledge of displacive phase transformations in non-metals (in particular, in ceramics) is reviewed. Using the tetragonal-to-monoclinic transformation in zirconia (ΔV = 4.9% at room temperature) as a model system, the factors controlling the metastability of confined particles are discussed, i.e. matrix constraint, chemical composition position and nucleation barrier to the transformation. The model for martensitic nucleation in ceramics is based on a localized soft mode mechanism at strain singularities or concentrations in faceted particles. Other potential transformation togerther alternative to zirconia have been identified. For the first time, preliminary mechanical toughness data using the new tougheners is briefly presented. Composites of 20wt.% BTb2O3 in 80 vol.% MgO causes a thresfold increase at 1400°C. Monoclinic (β) dicalcium silicate dispersed in calcium zirconate exhibits a fivefold increase in toughness. Other new materials including refractory sulfides are examined from the point of view of transformation toughening. The application of high pressures during processing makes it feasible to alter thermodynamic phase fields and to develop yet other new transformation-toughened composites. © 1990.
引用
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页码:249 / 255
页数:7
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