Crystallization Kinetics of Fe76.5−x C6.0Si3.3B5.5P8.7Cu x (x = 0, 0.5, and 1 at. pct) Bulk Amorphous Alloy

Abstract

The influence of Cu on crystallization kinetics of Fe76.5−x C6.0Si3.3B5.5P8.7Cu x (x = 0, 0.5, and 1 at. pct) bulk amorphous alloys was investigated by isothermal and isochronal differential scanning calorimetry combined with X-ray diffraction. The thermal analysis revealed that the crystallization of the amorphous matrix proceeds through at least two exothermic events. The Cu-free glassy alloy forms by primary crystallization the metastable Fe23C6 phase, while upon 0.5 at. pct Cu addition the primary crystallized phase is α-Fe. The activation energy for crystallization, calculated using both Kissinger and Ozawa methods, decreases from about 500 kJ/mol to about 330 kJ/mol. Further increase of Cu addition to 1 at. pct promotes the concomitant crystallization of several phases, as α-Fe, FeB, Fe3C, and Fe2P. In order to understand the crystallization behavior of the alloys as a function of Cu content, the Avrami exponent n, evaluated from the Johnson–Mehl–Avrami equation, was in details analyzed. The current study reveals that the minor Cu addition plays a crucial role at the initial stage of the crystallization. Among the studied alloys, the glassy samples with 0.5 at. pct Cu addition have the optimum compositional condition for the single α-Fe formation with a high nucleation rate.