Liquid phase separation in AlCrFeNiMo0.3 high-entropy alloy

2019 ◽  
Vol 112 ◽  
pp. 106517 ◽  
Author(s):  
A. Munitz ◽  
I. Edry ◽  
E. Brosh ◽  
N. Derimow ◽  
B.E. MacDonald ◽  
...  
2017 ◽  
Vol 86 ◽  
pp. 110-115 ◽  
Author(s):  
Tong Guo ◽  
Jinshan Li ◽  
Jun Wang ◽  
Yi Wang ◽  
Hongchao Kou ◽  
...  

Crystals ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 527 ◽  
Author(s):  
Takeshi Nagase ◽  
Mitsuharu Todai ◽  
Takayoshi Nakano

The liquid phase separation (LPS) behavior in Co-Cr-based high-entropy alloys (HEAs) is an important target for the development of Co-Cr-based HEAs for metallic biomaterials (BioHEAs). The solidification microstructure in Ag-Co-Cr-Fe-Mn-Ni-Ag, Co-Cr-Cu-Fe-Mn-Ni-Cu, and Co-Cr-Cu-Fe-Mn-Ni-B HEAs, which were designed as the combination of the equiatomic CoCrFeMnNi with Ag, Cu, and the interstitial element of B, was investigated as the fundamental research of LPS in Co-Cr-based HEAs. Ingots of equiatomic AgCoCrFeMnNi, equiatomic CoCrCuFeMnNi, non-equiatomic CoCrCuxFeMnNi (x = 2, 3), and CoCrCuxFeMnNiB0.2 (x = 1, 2, 3) with a small amount of B were fabricated using the arc-melting process. A macroscopic phase-separated structure was observed in the ingots of the equiatomic AgCoCrFeMnNi and CoCrCuxFeMnNiB0.2 (x = 2, 3) HEAs. The addition of a small amount of B enhanced the LPS tendency in the Co-Cr-Fe-Mn-Ni-Cu HEAs. The LPS behavior was discussed through the heat of mixing and computer coupling of phase diagrams and thermochemistry (CALPHAD).


2016 ◽  
Vol 77 ◽  
pp. 41-45 ◽  
Author(s):  
W.L. Wang ◽  
L. Hu ◽  
S.B. Luo ◽  
L.J. Meng ◽  
D.L. Geng ◽  
...  

2016 ◽  
Vol 72 ◽  
pp. 44-52 ◽  
Author(s):  
N. Liu ◽  
P.H. Wu ◽  
P.J. Zhou ◽  
Z. Peng ◽  
X.J. Wang ◽  
...  

2018 ◽  
Vol 941 ◽  
pp. 1238-1241 ◽  
Author(s):  
Takeshi Nagase

Liquid phase separation is a common phenomenon observed in various types of condensed matter, including metals. The microstructure of Co-Cr-Mn-Fe-Ni-Cu and Co-Cr-Fe-Mn-Ni-Ag high entropy alloys (HEAs) with liquid phase separation was investigated. Dual fcc phases were observed in CoCrFeMnNiAg, CoCrFeMnNiCu, and CoCrFeMnNiCu2HEAs. A macroscopically phase separated structure formed via liquid phase separation was observed in CoCrFeMnNiAg HEA, and conventional dendritic structures were observed in CoCrFeMnNiCu and CoCrFeMnNiCu2HEAs.


Entropy ◽  
2018 ◽  
Vol 20 (11) ◽  
pp. 890 ◽  
Author(s):  
Nicholas Derimow ◽  
Reza Abbaschian

It has been 14 years since the discovery of the high-entropy alloys (HEAs), an idea of alloying which has reinvigorated materials scientists to explore unconventional alloy compositions and multicomponent alloy systems. Many authors have referred to these alloys as multi-principal element alloys (MPEAs) or complex concentrated alloys (CCAs) in order to place less restrictions on what constitutes an HEA. Regardless of classification, the research is rooted in the exploration of structure-properties and processing relations in these multicomponent alloys with the aim to surpass the physical properties of conventional materials. More recent studies show that some of these alloys undergo liquid phase separation, a phenomenon largely dictated by low entropy of mixing and positive mixing enthalpy. Studies posit that positive mixing enthalpy of the binary and ternary components contribute substantially to the formation of liquid miscibility gaps. The objective of this review is to bring forth and summarize the findings of the experiments which detail liquid phase separation (LPS) in HEAs, MPEAs, and CCAs and to draw parallels between HEAs and the conventional alloy systems which undergo liquid-liquid separation. Positive mixing enthalpy if not compensated by the entropy of mixing will lead to liquid phase separation. It appears that Co, Ni, and Ti promote miscibility in HEAs/CCAs/MPEAs while Cr, V, and Nb will raise the miscibility gap temperature and increase LPS. Moreover, addition of appropriate amounts of Ni to CoCrCu eliminates immiscibility, such as in cases of dendritically solidifying CoCrCuNi, CoCrCuFeNi, and CoCrCuMnNi.


2017 ◽  
Vol 33 (11) ◽  
pp. 1352-1359 ◽  
Author(s):  
Z. Peng ◽  
N. Liu ◽  
S. Y. Zhang ◽  
P. H. Wu ◽  
X. J. Wang

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