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Effect of Cooling Method on Microstructure and Microhardness of CuCrFeMnNi High-Entropy Alloy

This study investigated four cooling methods for CuCrFeMnNi high-entropy alloy, namely, furnace cooling, air cooling, oil cooling, and water cooling (designated as FC, AC, OC, and WC, respectively), following a 12 h treatment at 800 °C. Results indicate that all four cooled alloys consisted of two F...

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Bibliographic Details
Published in:Coatings (Basel) 2024-07, Vol.14 (7), p.831
Main Authors: Zhou, Yajun, Zhao, Ruifeng, Geng, Hechuan, Ren, Bo, Liu, Zhongxia, Liu, Jianxiu, Jiang, Aiyun, Zhang, Baofeng
Format: Article
Language:English
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Summary:This study investigated four cooling methods for CuCrFeMnNi high-entropy alloy, namely, furnace cooling, air cooling, oil cooling, and water cooling (designated as FC, AC, OC, and WC, respectively), following a 12 h treatment at 800 °C. Results indicate that all four cooled alloys consisted of two FCC solid-solution phases (FCC1 and FCC2) and ρ phases. However, the FC alloy primarily contained FCC2 as the main phase and FCC1 as the secondary phase. The other three cooling methods yielded alloys with FCC2 as the primary phase and FCC1 as the secondary phase. With an increase in cooling rate, the content of the FCC1 phase gradually increased, that of the ρ phase initially decreased and then increased, and that of the FCC2 phase gradually decreased. The microstructure of the CuCrFeMnNi high-entropy alloy under the four cooling methods consisted of gray-black dendrites rich in Cr-Fe and white dendrites rich in Cu. Black ρ-phase particles predominated the dendrite region. As the cooling rate increased, the white interdendritic regions shrank, and the gray-black interdendritic regions expanded. The FC alloy exhibited the lowest microhardness at approximately 202.6 HV. As the cooling rate increased, the microhardness of the alloy progressively increased. The microhardness of the WC alloy was the highest, at approximately 355 HV. The strengthening mechanisms for all the alloys were primarily solid-solution strengthening and second-phase precipitation strengthening.
ISSN:2079-6412
2079-6412
DOI:10.3390/coatings14070831