铁钴基合金的无序→有序转变

D. W. Clegg, R. Buckley
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引用次数: 105

摘要

摘要研究了等原子铁钴合金和铁钴钒合金在400 ~ 600℃等温退火过程中的有序和反相畴聚结速率。实验技术包括x射线衍射(超晶格线强度、宽度和晶格参数)和磁饱和矩测量。在这些合金中,高达2.5%的钒含量对有序动力学没有显著影响。表明该体系中bcc→L20的转变是一个均匀的过程,而不是有序畴的成核和生长。反相畴聚结速率受钒的影响。在低于550°C的FeCo中,聚结速度非常快,而在高于550°C的FeCo和FeCo- v中,聚结速度相对较慢,并且服从线性(畴大小)与时间的关系。在比热、晶格参数和磁饱和测量的基础上,评价了钒在300 ~ 900℃范围内对有序平衡度的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Disorder → Order Transformation in Iron–Cobalt-Based Alloys
AbstractThe rates of ordering and antiphase domain coalescence during isothermal annealing of quenched equiatomic iron–cobalt and iron–cobalt–vanadium alloys have been studied in the range 400–600° C. Experimental techniques included X-ray diffraction (superlattice line intensity and breadth, and lattice parameter) and measurement of magnetic saturation moment. Amounts of vanadium up to 2.5% do not significantly affect the ordering kinetics in these alloys. It is suggested that the transformation bcc → L20 in this system occurs by a homogeneous process rather than by nucleation and growth of ordered domains. Rates of antiphase domain coalescence are affected by vanadium. Coalescence is very rapid in FeCo below 550°C but is relatively slow in FeCo and FeCo-V above 550°C, when a linear (domain size) vs. time relationship is obeyed. The effect of vanadium on the equilibrium degree of order in the range 300–900°C has been assessed on the basis of specific-heat, lattice-parameter, and magnetic-saturation measu...
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