Abstract

In this study, nano-CeO 2 particles as nucleating agents were incorporated into Ni625 alloy powder by ball milling method, with the aim of inhibiting occurrence of liquation crack during Ni625 alloy laser cladding. The differences in microstructure, electrochemical performance and tribological performance between Ni625 and Ni625 + 0.2 wt%CeO 2 cladding layers were studied and compared. The results from scanning electron microscope (SEM) and electron backscattered diffraction (EBSD) analyses clearly revealed that liquation crack in the lap zone between scanning tracks of the Ni625 cladding layer was caused by successive γ + Laves eutectic structure at the boundary of coarse grains. CeO 2 with high melting point and low Gibbs free energy had good stability, and the two-dimensional disregistry between CeO 2 and Ni625 alloy was 5.9%, which made the nano-CeO 2 particles promote the heterogeneous nucleation of Ni625 alloy. Benefiting from heterogeneous nucleation, the Ni625 + 0.2 wt%CeO 2 cladding layer was without liquation crack and had larger equiaxed zone and finer grains. Moreover, the γ + Laves eutectic structure at grain boundary changed from successive distribution to discrete distribution and its content reduced, which indicated that elemental segregation of Mo and Nb during solidification was improved. The results of electrochemistry, microhardness and friction wear tests showed that the Ni625 + 0.2 wt%CeO 2 cladding layer had large charge transfer resistance, higher microhardness and less wear mass loss, which signified that it had better corrosion resistance and wear resistance. • Liquation crack in the lap zone was clearly characterized by SEM and EBSD. • Nano-CeO 2 added by ball milling effectively refined grains of the cladding layer. • The liquation crack was inhibited as grain size and Laves phase content decreased. • The two-dimensional lattice disregistry between CeO 2 and Ni625 was revealed.

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