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Boronizing treatment has been considered as a promising strategy to enhance the surface hardness, self-lubrication and wear resistance of high entropy alloy (HEA), endowing the advancements of HEA in engineering applications. However, the anti-friction, anti-wear and corrosion resistance properties of the boronized HEA in sulfuric acid and seawater environments remain unclear. Here, the self-lubrication and corrosion resistance of the boronized CoCrFeNiMn HEA in these corrosive media were studied to assess the applicable environments. Firstly, a boronized layer with thickness of approximately 25 μm on the CoCrFeNiMn HEA surface was fabricated using the powder-pack boronizing treatment. Tribological assessments demonstrated exceptional self-lubricating properties of boronized HEA in various liquid conditions, with over 30 % reduced friction coefficients and over 80 % decreased wear rates. XPS analysis confirmed the formation of a boron-containing tribofilm, enhancing self-lubrication and reducing friction and wear in liquid environments. However, electrochemical tests indicated that the corrosion resistance of the boronized HEA was significantly affected by the liquid medium. The impedance value (|Z|) of boronized HEA decreased to 4.6 % of that of the original HEA in 3.5 wt% NaCl solution, revealing poor corrosion resistance. Conversely, an enhancement of corrosion resistance was observed in 0.05 M H 2 SO 4 solutions with the increase of the |Z| value by 8 times. Therefore, for applications requiring service safety, boronizing HEAs are more suitable for acidic environments, but not in seawater environments, offering valuable insights for the industrial application of CoCrFeNiMn HEA in reducing friction and wear. • The COF of boronized HEA is over 30 % lower than original HEA in liquid conditions. • The tribofilm (composed of H 3 BO 3 and B 2 O 3) significantly reduce friction and wear. • Boronized HEAs are more suitable for acidic environments, but not in seawater. [ABSTRACT FROM AUTHOR]

Boronizing has been considered as a promising strategy to enhance the surface hardness and corrosion resistance of the new emerged alloys, like CoCrNi medium-entropy alloy (MEA). However, recent studies showed that a brittle silicide layer was generated on the surface for Ni-containing alloys boronizied with the SiC-containing powder (SiC+KBF 4 +B 4 C). In this study, Si-free powder packing (900 °C 4 h) and electrochemical boronizing (900 °C 30 min) methods were explored to obtain the boronized layer for CoCrNi MEA. The morphology, element distributions and phases of the boronized layer were characterized by Scanning Electron Microscopy (SEM) and Energy Dispersive Spectrometer (EDS) and X-ray diffraction (XRD). The results show that the powder-pack boronizing method with 90 wt% B 4 C + 10 wt% NaBF 4 (B 4 C) and electrochemical (EC) methods have the thickest boronized layer (~70 μm) with hardness of about 22 GPa. The boronized layer is dominated by columnar CrB and Co 2 B with obvious preferred orientation and strong texture. In addition, CoB, Ni 2 B and Ni 3 B also exists in the boronized layer, and these two optimal boronizing processes avoid the influence of Si. This study shows that the B 4 C and EC boronizing methods can be considered as the viable alternative strategy for the preparation of strengthened layers. • The optimal boronizing methods were selected to obtain the strengthened layers. • Si-free boride layers were observed on the CoCrNi MEA surface. • The surface hardness reached to 17–22 GPa. • Borides in the boronized layer have obvious preferred orientation and strong texture. [ABSTRACT FROM AUTHOR]

Boronizing has been considered as a promising strategy to enhance the surface hardness and corrosion resistance of the new emerged alloys, like CoCrNi medium-entropy alloy (MEA). However, recent studies showed that a brittle silicide layer was generated on the surface for Ni-containing alloys boronizied with the SiC-containing powder (SiC+KBF 4 +B 4 C). In this study, Si-free powder packing (900 °C 4 h) and electrochemical boronizing (900 °C 30 min) methods were explored to obtain the boronized layer for CoCrNi MEA. The morphology, element distributions and phases of the boronized layer were characterized by Scanning Electron Microscopy (SEM) and Energy Dispersive Spectrometer (EDS) and X-ray diffraction (XRD). The results show that the powder-pack boronizing method with 90 wt% B 4 C + 10 wt% NaBF 4 (B 4 C) and electrochemical (EC) methods have the thickest boronized layer (~70 μm) with hardness of about 22 GPa. The boronized layer is dominated by columnar CrB and Co 2 B with obvious preferred orientation and strong texture. In addition, CoB, Ni 2 B and Ni 3 B also exists in the boronized layer, and these two optimal boronizing processes avoid the influence of Si. This study shows that the B 4 C and EC boronizing methods can be considered as the viable alternative strategy for the preparation of strengthened layers. • The optimal boronizing methods were selected to obtain the strengthened layers. • Si-free boride layers were observed on the CoCrNi MEA surface. • The surface hardness reached to 17–22 GPa. • Borides in the boronized layer have obvious preferred orientation and strong texture. [ABSTRACT FROM AUTHOR]