Cd0.85-xMnxZn0.15Te (x = 0.05-0.20)合金熔化结晶过程动力学参数

S. M. Rusnak, A. V. Matviy, V. V. Kopach, O. Kopach, L. Shcherbak, P. Fochuk
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摘要

采用差热分析(DTA)方法研究了Cd0.85-xMnxZn0.15Te (x = 0.05 ~ 0.20)合金在不同加热/冷却速率下的熔化和结晶动力学参数。Cd0.85-xMnxZn0.15Te合金是在防止成分升华的高梯度垂直炉中合成的。DTA是在一个自动系统中进行的。加热和冷却速度分别为5和10°С/min,停留时间分别为10、30和60分钟。DTA以两种不同的方式处理。采用第一种处理方法,发现Cd0.80Mn0.05Zn0.15Te合金熔体在过冷状态下结晶,并在熔体过温高于12°С时发生结晶。但当熔体过热到12℃时,合金的“负”过冷效应与合金的熔化温度相比是存在的,这是两相合金(固相-熔体)在这些温度下的证据。随着保温温度的升高,结晶温度降低,结晶速率增大。我们研究了结晶效应的面积随着保温温度的升高而增大。对于第二种处理方法,我们发现了Cd0.80Mn0.05Zn0.15Te加热过程中合金的固态体积分数(φ固态)与中间停留温度的关系。结果表明,随着熔体停留温度的升高,熔体在1117℃附近才达到完全均匀化。因此,根据我们之前的研究可知,Cd1-x-уMnxZnyTe合金的熔化温度随着ZnTe浓度的增加而升高:Cd0.95-xMnxZn0.05Te合金的熔化温度为~1100 ~1102°С (x=0.05 ~ 0.30), Cd0.90-xMnxZn0.10Te合金的熔化温度为~1102°С (x=0.05 ~ 0.30), Cd0.80Mn0.05Zn0.15Te合金的熔化温度为~1116 ~ 1119°С。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Kinetic parameters of Cd0.85-xMnxZn0.15Te (x = 0.05-0.20) alloys melting and crystallization processes
The kinetic parameters of melting and crystallization of Cd0.85-xMnxZn0.15Te (x = 0.05-0.20) alloys were investigated by the differential thermal analysis (DTA) method at different heating/cooling rates. Cd0.85-xMnxZn0.15Te alloys were synthesized from elementary materials in a vertical furnace with a high-gradient temperature that prevented the sublimation of the components. The DTA was carried out in an automatic system. The heating and cooling rates were 5 and 10°С/min, and the dwell time was 10, 30 and 60 minutes. The DTA were processed in two different ways. Using the first treatment method we found that the melt of the Cd0.80Mn0.05Zn0.15Te alloy crystallize with the supercooling, and it occurs at melt superheating higher than 12 °С. But the melt’s “negative” supercooling effect is present for alloy when the melt are superheated to 12 °C compared to the melting temperature of the alloy, which is evidence of two-phase alloy (solid phase - melt) at these temperatures. Also we determined that as the holding temperature increases the crystallization temperature decreases and the crystallization rate increases. We investigated that the area of the crystallization effect increases with increasing holding temperature. Concerning on the second treatment method we found the dependence of the solid-state volume fraction (φsolid state) versus the intermediate dwell temperature of the alloy during the heating process for Cd0.80Mn0.05Zn0.15Te. It shows that increasing of the melt-dwell temperature led to the melts full homogenization only near 1117 °C. Thus according to our previous researches we can say that the Cd1-x-уMnxZnyTe alloy’s melting temperature increases with ZnTe concentration increasing: ~1100-1102°С for Cd0.95-xMnxZn0.05Te alloys (x=0.05-0.30), ~1102-1104°С for Cd0.90-xMnxZn0.10Te alloys (x=0.05-0.30) and ~1116-1119°С for Cd0.80Mn0.05Zn0.15Te alloys.
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