差示扫描量热法
材料科学
成核
结晶
无定形固体
合金
热稳定性
扫描电子显微镜
退火(玻璃)
非晶态金属
分析化学(期刊)
能量色散X射线光谱学
结晶学
冶金
化学工程
化学
复合材料
热力学
物理
工程类
有机化学
色谱法
作者
Hong Haï Nguyen,Nguyen Thi Hoang Oanh,Nguyễn Hoàng Việt
标识
DOI:10.1088/2053-1591/ad513c
摘要
Abstract The thermal stability of mechanically alloyed amorphous Al-Fe-based alloy powders, with nominal compositions Al 82 Fe 16 Ce 2 and Al 82 Fe 14 Mn 2 Ce 2 , was investigated using differential scanning calorimetry (DSC), x-ray diffraction (XRD), and scanning electron microscopy (SEM) complemented by energy-dispersive x-ray spectroscopy (EDX). Analysis through DSC indicated that both Al 82 Fe 16 Ce 2 and Al 82 Fe 14 Mn 2 Ce 2 alloys undergo a two-stage crystallization process. Notably, the initial crystallization temperatures for the Al 82 Fe 16 Ce 2 and Al 82 Fe 14 Mn 2 Ce 2 alloys were determined to be approximately 525 °C and 550 °C, respectively. This high thermal stability is attributed to the delayed nucleation process induced by the presence of Ce and Mn within the Al-Fe matrix. During polymorphic crystallization, distinct phases such as β -AlFe, Al 13 Fe 4 for Al 82 Fe 16 Ce 2 , and β -Al(Fe, Mn), Al 13 Fe 4 , Al 10 CeMn 2 for Al 82 Fe 14 Mn 2 Ce 2 were identified. Furthermore, post-annealing of these amorphous alloy powders at elevated temperatures of 600, 700, and 800 °C led to distinct morphological characteristics based on the alloy composition. For Al 82 Fe 16 Ce 2 , the particles preserved a nearly spherical morphology, with size distributions ranging from 1 to 5 μ m. In contrast, for Al 82 Fe 14 Mn 2 Ce 2 , the particles exhibited an irregular shape with a broader size range of 1 to 15 μ m.
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