Constrained Dendritic Growth and Solute Concentration Effects in Rapidly Solidified Co-Cr Alloys

2019 ◽  
Vol 50 (5) ◽  
pp. 2272-2278
Author(s):  
A. L. Ramirez-Ledesma ◽  
H. F. Lopez ◽  
J. A. Juarez-Islas
1994 ◽  
Vol 42 (5) ◽  
pp. 1653-1660 ◽  
Author(s):  
Shu-Zu Lu ◽  
J.D. Hunt ◽  
P. Gilgien ◽  
W. Kurz

1981 ◽  
Vol 9 ◽  
Author(s):  
M. E. Glicksman ◽  
Narsingh Bahadur Singh ◽  
M. Chopra

ABSTRACTExtensive experimentation has been carried out in which the kinetics and morphology of dendritic growth were measured as a function of thermal supercooling, solute concentration, and spatial orientation of the dendritic growth axis. The crystal growth system studied is succinonitrile [NC(CH2)2CN] with additions of argon (up to 0.1 mole %). This system is especially useful as a model for alloy studies because kinetic data are available for high purity (7–9's) succinonitrile. The addition of argon provides a simple, controllable dilute solute that now permits the first comparably detailed dendritic growth studies on binary alloys.One dramatic influence of the solute, at fixed thermal supercooling, is to increase the growth velocity (to a maximum) and correspondingly decrease intrinsic crystal dimensions (tip radius). Morphological measurements will be described in detail relating tip size, perturbation wavelength, supercooling, and solute concentration. The analysis of these effects based on morphological stability theory will also be discussed. Finally, experiments permitting the separation of convective and diffusive heat transport during crystal growth of succinonitrile will be described briefly. These studies clearly underscore the importance of gravitationally-induced buoyancy effects on crystal growth kinetics and morphology.


2016 ◽  
Vol 668 ◽  
pp. 46-55 ◽  
Author(s):  
Jie Ma ◽  
Bo Wang ◽  
Shunli Zhao ◽  
Guangxin Wu ◽  
Jieyu Zhang ◽  
...  

1960 ◽  
Vol 38 (8) ◽  
pp. 1077-1088 ◽  
Author(s):  
T. S. Plaskett ◽  
W. C. Winegard

The transition from cellular growth to dendritic growth was investigated for dilute binary alloys of zone-refined tin with lead, bismuth, and antimony in terms of the rate of growth R, the temperature gradient in the liquid ahead of the solid-liquid interface G, and the solute concentration C0. It was found that a previous relationship describing the transition for lead base alloys applied, at least to a first approximation, for the low solute concentration tin results. At the high concentrations of solute, however, it was necessary to introduce another variable, namely the cell size at transition dt. The transition relationships only applied for alloy systems with a distribution coefficient k0, less than unity. For systems with k0 > 1 (antimony in tin) a k0 < 1 was used which was equivalent to the k0 > 1. A method is described for determining this "equivalent k0".


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