烧结
晶粒生长
活化能
材料科学
晶界扩散系数
粒度
晶界
陶瓷
晶格扩散系数
扩散
动能
分析化学(期刊)
矿物学
相(物质)
冶金
有效扩散系数
微观结构
物理化学
化学
热力学
物理
有机化学
磁共振成像
放射科
医学
量子力学
色谱法
作者
Tetsuya Senda,Richard C. Bradt
标识
DOI:10.1111/j.1151-2916.1990.tb05099.x
摘要
Grain growth in a high‐purity ZnO and for the same ZnO with Bi 2 O 3 additions from 0.5 to 4 wt% was studied for sintering from 900° to 1400°C in air. The results are discussed and compared with previous studies in terms of the phenomenological kinetic grain growth expression: G n — G n 0 = K 0 t exp(— Q/RT ). For the pure ZnO, the grain growth exponent or n value was observed to be 3 while the apparent activation energy was 224 ± 16 kJ/mol. These parameters substantiate the Gupta and Coble conclusion of a Zn 2+ lattice diffusion mechanism. Additions of Bi 2 O 3 to promote liquidphase sintering increased the ZnO grain size and the grain growth exponent to about 5, but reduced the apparent activation energy to about 150 kJ/mol, independent of Bi 2 O 3 content. The preexponential term K 0 was also independent of Bi 2 O 3 content. It is concluded that the grain growth of ZnO in liquid‐phase‐sintered ZnO‐Bi 2 O 3 ceramics is controlled by the phase boundary reaction of the solid ZnO grains and the Bi 2 O 3 ‐rich liquid phase.
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