Kinetics and formation mechanism of amorphous Fe52Nb48 alloy powder fabricated by mechanical alloying

被引:23
作者
El-Eskandarany, MS [1 ]
Bahgat, AA
Gomaa, NS
Eissa, NA
机构
[1] Al Azhar Univ, Fac Engn, Dept Min Met & Petr Engn, Cairo 11371, Egypt
[2] Al Azhar Univ, Fac Sci, Dept Phys, Mossbauer Lab, Cairo 11884, Egypt
关键词
amorphous steel alloys; multilayered diffusion couples; ball milling; alloying elements; Mossbauer spectroscopy; morphology; crystallization;
D O I
10.1016/S0925-8388(99)00222-4
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A single phase amorphous Fe,,Nb,, alloy has been synthesized through a solid state interdiffusion of pure polycrystalline Fe and Nh powders at room temperature, using a high-energy ball-milling technique. The mechanisms of metallic glass formation and competing crystallization processes in the mechanically deformed composite powders have been investigated by means of X-ray diffraction, Mossbauer spectroscopy, differential thermal analysis, scanning electron microscopy and transmission electron microscopy. The numerous intimate layered composite particles of the diffusion couples that formed during the first and intermediate stages of milling time (0-56 ks), are intermixed to form amorphous phase(s) upon heating to about 625 K by so-called thermally assisted solid state amorphization, TASSA. The amorphization heat of formation for binary system via the TASSA, Delta H-a, was measured directly as a function of the milling time. Comparable with the TASSA, homogeneous amorphous alloys were fabricated directly without heating the composite multilayered particles upon milling these particles for longer milling time (86 ks-144 ks). The amorphization reaction here is attributed to the mechanical driven solid state amorphization. This single amorphous phase transforms into an order phase (mu phase) upon heating at 1088 K (crystallization temperature, T-x) with enthalpy change of crystallization, Delta H-x, of -8.3 kJ mol(-1). (C) 1999 Elsevier Science S.A. All rights reserved.
引用
收藏
页码:181 / 190
页数:10
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