TY - JOUR
T1 - Cuboid-like nanostructure strengthened equiatomic Ti–Zr–Nb–Ta medium entropy alloy
AU - Nguyen, V. T.
AU - Qian, M.
AU - Shi, Z.
AU - Tran, X. Q.
AU - Fabijanic, D. M.
AU - Joseph, J.
AU - Qu, D. D.
AU - Matsumura, S.
AU - Zhang, C.
AU - Zhang, F.
AU - Zou, J.
N1 - Funding Information:
This work was supported by the Australian Research Council (ARC) through ARC LP130100913 and the Baosteel-Australia Joint Research and Development Centre through BA110014LP . VTN thanks the International Postgraduate Research Scholarship (IPRS) Program for providing him with a PhD scholarship. MQ and DMF further acknowledge the support from the Australian-India Strategic Research Fund ( AISRF53731 -Advanced manufacturing of new high entropy alloys). The Australian Microscopy & Microanalysis Research Facility is acknowledged for providing characterization facilities.
Publisher Copyright:
© 2020 Elsevier B.V.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020/11/4
Y1 - 2020/11/4
N2 - This study investigates the effect of annealing treatment on the phase transformation and mechanical properties of the equiatomic TiZrNbTa MEA from room temperature to 1200 °C. After annealing at 1200 °C for 24h, the single solid-solution body-centred cubic (BCC) phase in the as-cast Ta25Zr25Nb25Ti25 transformed into an extremely high number density (~103/μm2) of Ta–Nb-rich BCC nanocuboidal phase (28 ± 10 nm square, BCC1) and a nanostrip-like Zr-rich BCC phase (3 ± 2 nm thick, BCC2). The phase separation from BCC to BCC1 and BCC2 arises from two primary reasons: (i) the high positive mixing enthalpy of both Ta–Zr and Nb–Zr (strong tendency to separation between each pair), and (ii) the 3–4 orders of magnitude higher mobility of Zr than Ta, Nb and Ti in these MEAs (kinetically driven). Detailed CALPHAD simulations of phase formation in this MEA agreed with experiments and provided insightful phase transformation details. The calculated diffusion distance of Zr (~4.1 nm) from the CALPHAD data corresponds to the measured Zr-rich nanostrip thickness (3 ± 2 nm). The nanocuboidal BCC1-BCC2 structure exhibited 112<111>-type of twinning deformation under compression at room temperature. The Ta25Zr25Nb25Ti25 MEA retained yield strength of ~410 MPa at 1000 °C and ~210 MPa at 1200 °C. The phase transformation during cooling after annealing and the microstructural evolution during compression at temperatures from 600 °C to 1200 °C were characterized and discussed in detail.
AB - This study investigates the effect of annealing treatment on the phase transformation and mechanical properties of the equiatomic TiZrNbTa MEA from room temperature to 1200 °C. After annealing at 1200 °C for 24h, the single solid-solution body-centred cubic (BCC) phase in the as-cast Ta25Zr25Nb25Ti25 transformed into an extremely high number density (~103/μm2) of Ta–Nb-rich BCC nanocuboidal phase (28 ± 10 nm square, BCC1) and a nanostrip-like Zr-rich BCC phase (3 ± 2 nm thick, BCC2). The phase separation from BCC to BCC1 and BCC2 arises from two primary reasons: (i) the high positive mixing enthalpy of both Ta–Zr and Nb–Zr (strong tendency to separation between each pair), and (ii) the 3–4 orders of magnitude higher mobility of Zr than Ta, Nb and Ti in these MEAs (kinetically driven). Detailed CALPHAD simulations of phase formation in this MEA agreed with experiments and provided insightful phase transformation details. The calculated diffusion distance of Zr (~4.1 nm) from the CALPHAD data corresponds to the measured Zr-rich nanostrip thickness (3 ± 2 nm). The nanocuboidal BCC1-BCC2 structure exhibited 112<111>-type of twinning deformation under compression at room temperature. The Ta25Zr25Nb25Ti25 MEA retained yield strength of ~410 MPa at 1000 °C and ~210 MPa at 1200 °C. The phase transformation during cooling after annealing and the microstructural evolution during compression at temperatures from 600 °C to 1200 °C were characterized and discussed in detail.
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U2 - 10.1016/j.msea.2020.140169
DO - 10.1016/j.msea.2020.140169
M3 - Article
AN - SCOPUS:85090403980
SN - 0921-5093
VL - 798
JO - Materials Science & Engineering A: Structural Materials: Properties, Microstructure and Processing
JF - Materials Science & Engineering A: Structural Materials: Properties, Microstructure and Processing
M1 - 140169
ER -