Improving strength-ductility synergy of TiNbVTa refractory high-entropy alloys at room temperature by Cr microalloying

IF 7 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
Shuyue Lv , Yongle Kou , Yukang Liu , Yuheng Zhang , Qinglin Li
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Abstract

Due to their excellent mechanical performance at elevated temperatures, TiNbVTa-based alloys have emerged as a focal point of research within the field of refractory high-entropy alloys (RHEAs). However, the intrinsic trade-off between strength and ductility in TiNbVTa alloys continues to limit their further development for ambient-temperature applications. In this study, a novel microalloying strategy is proposed by introducing chromium (Cr) to promote the formation of substitutional solid solutions, thereby enhancing the room-temperature mechanical properties of TiNbVTa-based RHEAs. To validate this approach, a series of (TiNbVTa)100-xCrx (x = 0, 0.35, and 0.7 at.%) RHEAs was systematically designed and synthesized. The results revealed that all the investigated alloys possessed a single body-centred cubic (BCC) phase structure. As the Cr content increased from 0 to 0.7 at.%, the ultimate tensile strength, yield strength, and elongation of the (TiNbVTa)100-xCrx alloys initially increased, followed by a subsequent decline. Notably, the (TiNbVTa)99.65Cr0.35 alloy exhibited exceptional room temperature mechanical performance, achieving a tensile yield strength of 903 ± 22 MPa and an elongation of 18.7 ± 2.6 %, both of which surpass previously reported values for TiNbVTa-based RHEAs. The enhancement in mechanical properties induced by Cr microalloying was ascribed to the synergistic contributions of the synergistic hindrance of dislocation motion by SROs and the lattice distortion field induced by Cr addition, impeded dislocation motion through the formation of dislocation rings, and the promotion of dislocation proliferation. Furthermore, this study introduces microalloying as an effective strategy for concurrently improving both the strength and ductility of RHEAs.
Cr微合金化提高室温下TiNbVTa难熔高熵合金的强度-塑性协同效应
由于其在高温下优异的力学性能,tinbva基合金已成为难熔高熵合金(RHEAs)领域的研究热点。然而,TiNbVTa合金在强度和延展性之间的内在权衡仍然限制了其在室温应用中的进一步发展。本研究提出了一种新的微合金化策略,通过引入铬(Cr)来促进取代固溶体的形成,从而提高tinbvta基RHEAs的室温力学性能。为了验证这种方法,使用了一系列(TiNbVTa)100-xCrx (x = 0,0.35和0.7 at)。%)系统地设计和合成了RHEAs。结果表明,所研究的合金均具有单体心立方(BCC)相结构。随着Cr含量从0增加到0.7 at。%时,(TiNbVTa)100-xCrx合金的极限抗拉强度、屈服强度和伸长率先升高后下降。值得注意的是,(TiNbVTa)99.65Cr0.35合金表现出优异的室温力学性能,抗拉屈服强度为903±22 MPa,伸长率为18.7±2.6%,这两个数值都超过了先前报道的基于TiNbVTa的RHEAs。Cr微合金化引起的力学性能增强归因于sro对位错运动的协同阻碍和Cr添加引起的晶格畸变场的协同作用,通过位错环的形成阻碍了位错运动,促进了位错扩散。此外,本研究还介绍了微合金化作为同时提高流变合金强度和延展性的有效策略。
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来源期刊
Materials Science and Engineering: A
Materials Science and Engineering: A 工程技术-材料科学:综合
CiteScore
11.50
自引率
15.60%
发文量
1811
审稿时长
31 days
期刊介绍: Materials Science and Engineering A provides an international medium for the publication of theoretical and experimental studies related to the load-bearing capacity of materials as influenced by their basic properties, processing history, microstructure and operating environment. Appropriate submissions to Materials Science and Engineering A should include scientific and/or engineering factors which affect the microstructure - strength relationships of materials and report the changes to mechanical behavior.
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