TY - JOUR
T1 - Phase selection and characterization of Fe-based multi-component amorphous composite
AU - Zhang, P. C.
AU - Wang, H. P.
N1 - Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2022/4/6
Y1 - 2022/4/6
N2 - Phase selection and amorphous transition play a significant role for controlling of the microstructure and properties of multi-component alloys. In the present work, the solidified microstructure evolution of Fe52-xCo20NixB19Si5Nb4 (x = 7,12, labeled as 7 Ni, 12 Ni) alloys were studied in a wide range of cooling rate, and the effect of phase constitutions on the magnetic and micromechanical properties were systematically investigated. The results show that the microstructures of the two master alloys are composed of α-Fe, γ-Fe, Fe2B and Nb6Co16Si7 phases. As the solid solubility increases, the content of the intermetallic Nb6Co16Si7 phase decreases or even disappears, while the metastable Fe3B phase and Fe23B6 phase grow competitively. With the rise of the cooling rate, there is a transition from eutectic microstructure to internal amorphous structure plus peripheral crystalline/amorphous composite, and then to complete amorphous state in the two alloys. For the 7 Ni alloy, when the droplet diameter reduces, the coercivity of the alloy decreases continuously. As the content of the main magnetic α-Fe phase decreases, the saturation magnetization of the alloy diminishes firstly, and then slightly heightens when it is completely amorphous. From the perspective of solid solubility, the difference in hardness of the α-Fe and Fe2B phases with the undercooling is clarified. The hardness of the amorphous phase is slightly lower than that of the Fe2B phase. Finally, the nanoindentation technique was used to explore the indentation size effect and creep behavior of amorphous composite under different peak loads and different loading rates. As the peak load decreases or the loading rate increases, the hardness and elastic modulus of the alloy enhance, while the maximum creep displacement, stress factor and activation volume all increase with the rise of the peak load.
AB - Phase selection and amorphous transition play a significant role for controlling of the microstructure and properties of multi-component alloys. In the present work, the solidified microstructure evolution of Fe52-xCo20NixB19Si5Nb4 (x = 7,12, labeled as 7 Ni, 12 Ni) alloys were studied in a wide range of cooling rate, and the effect of phase constitutions on the magnetic and micromechanical properties were systematically investigated. The results show that the microstructures of the two master alloys are composed of α-Fe, γ-Fe, Fe2B and Nb6Co16Si7 phases. As the solid solubility increases, the content of the intermetallic Nb6Co16Si7 phase decreases or even disappears, while the metastable Fe3B phase and Fe23B6 phase grow competitively. With the rise of the cooling rate, there is a transition from eutectic microstructure to internal amorphous structure plus peripheral crystalline/amorphous composite, and then to complete amorphous state in the two alloys. For the 7 Ni alloy, when the droplet diameter reduces, the coercivity of the alloy decreases continuously. As the content of the main magnetic α-Fe phase decreases, the saturation magnetization of the alloy diminishes firstly, and then slightly heightens when it is completely amorphous. From the perspective of solid solubility, the difference in hardness of the α-Fe and Fe2B phases with the undercooling is clarified. The hardness of the amorphous phase is slightly lower than that of the Fe2B phase. Finally, the nanoindentation technique was used to explore the indentation size effect and creep behavior of amorphous composite under different peak loads and different loading rates. As the peak load decreases or the loading rate increases, the hardness and elastic modulus of the alloy enhance, while the maximum creep displacement, stress factor and activation volume all increase with the rise of the peak load.
KW - Amorphous evolution
KW - Microscopic hardness
KW - Phase selection
KW - Rapid solidification
UR - http://www.scopus.com/inward/record.url?scp=85124905388&partnerID=8YFLogxK
U2 - 10.1016/j.msea.2022.142840
DO - 10.1016/j.msea.2022.142840
M3 - 文章
AN - SCOPUS:85124905388
SN - 0921-5093
VL - 839
JO - Materials Science and Engineering: A
JF - Materials Science and Engineering: A
M1 - 142840
ER -