RESUMO
In this study, graphene-oxide (GO)-reinforced Ti-Al-Sn-Zr-Mo-Nb-Si high-temperature titanium-alloy-matrix composites were fabricated by powder metallurgy. The mixed powders with well-dispersed GO sheets were obtained by temperature-controlled solution mixing, in which GO sheets adsorb on the surface of titanium alloy particles. Vacuum deoxygenating was applied to remove the oxygen-containing groups in GO, in order to reduce the introduction of oxygen. The compact composites with refined equiaxed and lamellar α phase structures were prepared by hot isostatic pressing (HIP). The results show that in-situ TiC layers form on the surface of GO and GO promotes the precipitation of hexagonal (TiZr)6Si3 particles. The composites exhibit significant improvement in strength and microhardness. The room-temperature tensile strength, yield strength and microhardness of the composite added with 0.3 wt% GO are 9%, 15% and 27% higher than the matrix titanium alloy without GO, respectively, and the tensile strength and yield strength at 600 °C are 3% and 21% higher than the matrix alloy. The quantitative analysis indicates that the main strengthening mechanisms are load transfer strengthening, grain refinement and (TiZr)6Si3 s phase strengthening, which accounted for 48%, 30% and 16% of the improvement of room-temperature yield strength, respectively.
RESUMO
Non-isothermal oxidation is one of the important issues for the safe application of Ti-Al alloys, so this study aimed to illustrate the non-isothermal oxidation behaviors and the corresponding mechanisms of a TiAl-based alloy in comparison with a Ti3Al-based alloy. The non-isothermal oxidation behaviors of Ti-46Al-2Cr-5Nb and Ti-24Al-15Nb-1.5Mo alloys in pure oxygen were comparatively investigated with a thermogravimetry-differential scanning calorimetry (TGA/DSC) simultaneous thermal analyzer heating from room temperature to 1450 °C with a heating rate of 40 °C/min. When the temperature rose above 1280 °C, the oxidation rate of the Ti-46Al-2Cr-5Nb alloy sharply increased and exceeded that of the Ti-24Al-15Nb-1.5Mo alloy owing to the occurrence of internal oxidation. When the temperature was higher than 1350 °C, the oxidation rate of the Ti-46Al-2Cr-5Nb alloy decreased obviously due to the generation of an oxygen-barrier ß-Al2TiO5-rich layer by a chemical reaction between Al2O3 and TiO2 in the oxide scale. Based on Wagner's theory of internal oxidation, the reason for the occurrence of internal oxidation in the Ti-46Al-2Cr-5Nb alloy is the formation of the α phase in the subsurface, while no internal oxidation occurred in the Ti-24Al-15Nb-1.5Mo alloy due to the existence of the ß phase in the subsurface with the enrichment of Nb and Mo.
RESUMO
Non-isothermal oxidation is one of the important issues related to the safe application of high-temperature titanium alloys, so this study focuses on the non-isothermal oxidation behavior and mechanism of near-α titanium alloys. The thermogravimetry-differential scanning calorimetry (TGA/DSC) method was used to study the non-isothermal oxidation behavior of TA29 titanium alloy heated from room temperature to 1450 °C at a heating rate of 40 °C/min under pure oxygen atmosphere. The results show that non-isothermal oxidation behavior can be divided into five stages, including no oxidation, slow oxidation, accelerated oxidation, severe oxidation and deceleration oxidation; for the three-layer TiO2 scale, Zr, Nb, Ta are enriched in the intermediate layer, while Al is rich in the inner layer and Sn is segregated at the oxide-substrate interface, which is related to their diffusion rates in the subsurface α case. The oxidation mechanism for each stage is: oxygen barrier effect of a thin compact oxide film; oxygen dissolution; lattice transformation accelerating the dissolution and diffusion of oxygen; oxide formation; oxygen barrier effect of recrystallization and sintering microstructure in outer oxide scale. The alloying elements with high valence state and high diffusion rate in α-Ti are favorable to slow down the oxidation rate at the stage governed by oxide formation.
