Characterization, thermodynamic analysis and magnetic investigation of new soft magnetic amorphous/nanocrystalline Co50Fe21Ti19Ta5B5 powders produced by mechanical alloying

被引:24
作者
Taghvaei, Amir Hossein [1 ]
Khoshrodi, Adel Mohammadalitabar [1 ]
机构
[1] Shiraz Univ Technol, Dept Mat Sci & Engn, Shiraz, Iran
关键词
Amorphization; Mechanical alloying; Microstructure; Magnetic measurements; BULK METALLIC GLASSES; FULLY DENSE BULK; THERMAL-STABILITY; AMORPHOUS-ALLOYS; PHASE; BORON; MICROSTRUCTURE; EVOLUTION; STRENGTH; NITROGEN;
D O I
10.1016/j.jallcom.2018.01.382
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
In this work, the microstructure, thermal stability and magnetic properties of a new Co50Fe21Ti19Ta5B5 alloy prepared by mechanical alloying (MA) were investigated. Quantitative X-ray diffraction (XRD) analysis performed via Rietveld refinement demonstrated a high glass-forming ability (GFA) of this alloy through a fast amorphization with a glass fraction of about 98 wt% after 20 h milling. In addition, a large driving force for amorphization in Co50Fe21Ti19Ta5B5 alloy was indicated via a great difference between the Gibbs free energy changes for amorphization (-68 kJ/mol) and solid-solution formation (-6 kJ/mol), calculated based on the extended Miedema's semi-empirical model. Thermal analysis confirmed a higher crystallization temperature of new alloy compared to some of mechanically alloyed Co-based glassy powders, recently produced. The presence of few remained nanocrystals with an average size of 5 nm and little un-dissolved boron nanoparticles inside the amorphous matrix were confirmed by high-resolution transmission electron microscopy (HRTEM) measurements. The magnetic measurements revealed that the powders after an optimized milling time and annealing condition show a promising magnetic softness. The new powders exhibited a larger saturation magnetization (78 Am2/kg) and significantly a lower coercivity (0.2 kA/m) with respect to the most of the Co-based amorphous powders prepared by MA. (c) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:887 / 896
页数:10
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