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Boronized alloys with high surface hardness has been revealed advance in enhancing the anti-wear performance of critical mechanic components. However, its application in industrial production is greatly limited due to the poor mechanical properties with crystallographic orientated brittle borides. In the present study, we demonstrated that high ductility and high strength were achieved for the boronized AlCoCrFeNi 2.1 eutectic high entropy alloy (EHEA) with the formation of nano-sized borides. The AlCoCrFeNi 2.1 EHEA was treated with electrochemical boronizing method, and its phase formation was studied by x-ray diffraction (XRD), electron back-scattered diffraction (EBSD) and focused ion beam-transmission electron microscope (FIB-TEM). Results show that the nano-grained of FeB, NiB and Cr 3 B 4 with size of about 135.5 nm were formed on the boronized layer with non-preferred crystallographic orientation of the phase. The surface hardness of boronized AlCoCrFeNi2.1 EHEA reached to about 18 GPa, being about 4 times higher than that of the original alloy. Further investigation by tensile testing shows that the tensile strength of boronized samples is about 1.2 GPa with a respectable ductility of about 16.04% (± 0.49) tensile ductility to failure. Meanwhile, extension test and digital image correlation (XTDIC) test shows that the boronized layer failed when the tensile ductility is about 5.1%. The disordered nano-grained in the boronized layer benefit in preventing the formation and propagation of cracks, which improved the ductility of the boronized AlCoCrFeNi 2.1 EHEAs. [Display omitted] • The nano-sized borides of FeB, NiB and Cr 3 B 4 with grain size about 135.5 nm was generated on the AlCoCrFeNi 2.1 EHEA surface. • The elongation and strength of boronized EHEA reach 16.04% and 1197 MPa, and the surface hardness reaches 21 GPa. • The fracture of the brittle boronized layer occurred at the strain of 5.1%. • The crystallographic non-oriented nano-sized borides significantly inhibition crack generation and propagation. [ABSTRACT FROM AUTHOR]

• Enhanced wear-resistance were achieved by reducing the content of Nb in TiZrHfNb. • The wear loss is related to the subsurface instabilities during friction. • Deformation-induced grain refinement and phase transformation enhance wear-resistance. A sliding enhanced wear-resistance can be significantly achieved by reducing the content of Nb element in TiZrHfNb refractory high entropy alloys (RHEAs). The wear loss reduced by half from TiZrHfNb to TiZrHfNb 0.4. The wear loss is directly related to the subsurface instabilities induced by plastic deformation during friction. The origins can be attributed to two factors: i) plastic deformation induced grain refinement; ii) deformation-induced BCC to HCP phase transformation. [ABSTRACT FROM AUTHOR]

A series of TiZrV 0.5 Nb 0.5 Al x refractory high entropy alloys were prepared by arc-metling, aiming to solve the problems of high density, poor oxidation and wear resistance of refractory high entropy alloys at elevated temperature. The microstructure, mechanical and tribological properties were investigated. The results indicate that the increase in Al addition could promote precipitation of Laves phase in the BCC matrix, thus regulation the mechanical properties. The tribology behavior is strongly dependent on the temperature. Below 400 °C, the wear mechanism is dominated by mechanical wear. In this case, the TiZrV 0.5 Nb 0.5 Al 0.25 alloy with high strength and good ductility at the same time, exhibits optimal wear resistance. When the temperature increases above to 600 °C, the coefficient of friction and the corresponding wear rate dramatically decrease with Al addition, which could be attributed to the preformed formation of dense and stable oxide glazed-layer before wear. Accordingly, the main wear mechanism changes from mechanical wear to oxidation wear. This study provides an effective strategy for improving wear resistance and oxidation resistance of refractory high entropy alloys in a wide temperature range. • Al-containing alloys hardly wear at 600 °C and 800 °C. • The high temperature worn surface of Al-containing alloy has a dense oxide layer. • The Al0.25 alloy has unique needle-like Laves phase and the best wear resistance. [ABSTRACT FROM AUTHOR]

The wear behaviors of γ-TiAl alloy with two typical microstructures, i.e., the lamellar colony microstructure (denoted as the HIPed sample) and the fine equiaxed microstructure (denoted as the heat-treated sample), were thoroughly studied during dry sliding test to resolve the microstructural feature dependence of wear mechanisms. Special efforts have been made to the subsurface stability during sliding by using electron backscatter diffraction (EBSD) techniques. It is demonstrated that both cases present a similarity in the friction coefficients but a disparity in the wear loss. The lower wear loss was achieved in the case of HIPed sample. This can be attributed to the various directions in the local strain induced by plastic deformation during sliding, the crystallographic structure and the coherent interface in the lamellar colony, leading to high resistance ability to the wear. For the case of heat-treated sample, the high plastic deformation ability in the α 2 grains along the surface and the equiaxed morphology generate to high ability to plastic deformation and sliding during friction, contributing to the high wear loss. However, the heat-treated sample presents a high subsurface structure stability according to the local misorientation analysis. The present results provide new information on wear mechanisms of γ-TiAl alloy and may offer a method to enhance its wear resistance by tailoring the microstructural features. • The wear loss in a dry sliding of a γ-TiAl alloy is evidenced to connect with microstructural feature. • Special efforts have been made to the subsurface stability during sliding by using EBSD techniques. • The lower wear loss was achieved in the case of the lamellar colony microstructure. • The fine globular microstructure presents a high subsurface structure stability. [ABSTRACT FROM AUTHOR]