材料科学
三元运算
相(物质)
接口(物质)
最大相位
钯
化学工程
结晶学
催化作用
冶金
碳化物
复合材料
有机化学
化学
计算机科学
工程类
程序设计语言
毛细管数
毛细管作用
作者
Karanam Bhanumurthy,Rainer Schmid‐Fetzer
出处
期刊:International Journal of Materials Research
[De Gruyter]
日期:1996-04-01
卷期号:87 (4): 244-253
被引量:11
标识
DOI:10.1515/ijmr-1996-870402
摘要
The phase diagram of Pd-Si-C was investigated by experimental methods (XRD, SEM/EDX) and approximate thermodynamic calculations. Based on these results several isothermal sections between 700 and 1000°C are developed. Bulk diffusion couples between Pd and monocrystalline SiC were studied in the same temperature range, 700 to 900°C. A comparison of reaction behaviour between monocrystalline 6H-SiC and ceramic HIP-SiC with Pd is given. The formation of periodic bands consisting of Pd 2 Si + C and Pd 2 Si is clearly observed in the Pd/6H-SiC diffusion zone. These periodic bands are obscured in the Pd/HIP-SiC diffusion couples. In addition, a fine periodic substructure in the two-phase layer (Pd 2 Si + C) is detected. Furthermore, at least a modest joining pressure may be required to produce the reaction zone and the periodic bands. The sequence of reaction layers as observed in the diffusion couples, SiC/C+Pd 2 Si/Pd 2 Si/-/C+Pd 2 Si/Pd 2 Si/Pd 3 Si/Pd, could be related to the isothermal section at 800°C. At 850 °C a liquid phase is formed in the diffusion zone. Interpretations pertaining to the observed diffusion paths are discussed based on the ternary solid state equilibria.
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