Link between the Dissolution Mechanisms of a Solid Metal in a Liquid Binary Alloy and the Short-range Order in the Melt

Author(s):  
Andre Coulet ◽  
Mohamed Hedibel ◽  
Robert Castanet
1988 ◽  
Vol 31 (8) ◽  
pp. 659-663 ◽  
Author(s):  
D. A. Badalyan ◽  
A. A. Muradyan ◽  
D. K. Melik-Vartanyan

1988 ◽  
Vol 145 (2) ◽  
pp. 525-534
Author(s):  
H. N. Nazareno ◽  
I. Fonseca Moreno ◽  
R. M. Ribeiro-Teixeira ◽  
J. R. Iglesias

2000 ◽  
Vol 644 ◽  
Author(s):  
Junji Saida ◽  
Mitsuhide Matsushita ◽  
Akihisa Inoue

AbstractIt is found that a nano icosahedral phase with diameters below 50 nm is formed as a primary phase in the Zr70Ni10M20, Zr70TM10Pd20, Zr70Au10Pd20 and Zr75Pt10Pd15 ternary and Zr70Pd30 binary glassy alloys. The nanoscale icosahedral phase in the diameter range below 10 nm was also found to be formed directly in the melt-spun Zr80Pt20 binary alloy. These icosahedral phases transform to the crystalline phase(s) at the higher annealing temperature. The nucleation kinetics for the precipitation of the icosahedral phase from supercooled liquid were examined in the Zr70Pd30 and Zr70Ni10Pd20 glassy alloys. It was clarified that the transformation of both alloys proceeds in the diffusion-controlled growth mode with increasing nucleation rate. The formation of the nanometer-scale icosahedral phase is due to the transformation mode. The activation energy of nucleation is evaluated to be 267 kJmol−1 for the binary alloy and 311 kJmol−1 for the ternary alloy. The difference between the two alloy systems seems to originate from the difference in the number of atoms for rearrgements in the nucleation mode. The short-range ordering is observed in the as-quenched Zr70Pd30 glassy alloy, which is indicative of the icosahedral structure. The formation of the nano-scale icosahedral phase in the Zr-based binary and ternary alloys is due to the existence of an icosahedral short-range order in the glassy or liquid state. It is suggested that the icosahedral short-range order is stabilized by the restraint of the long-range atomic rearrangements that lead to the transition to a periodic structure by the strong chemical affinities of Pd or Pt with Zr.


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