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In this experiment, Ti-44Al-9Nb-1Cr-0.2W-0.2Y alloy was prepared by the directional solidification method. The effect of different growth rates on tensile properties and microstructure orientation at high temperature was studied. Three kinds of alloys with different growth rates of 10 μm/s, 15 μm/s and 20 μm/s were prepared. The results show that the tensile properties of the alloy at 800 ℃ decrease with increasing growth rate, and recrystallization occurred at the position of intracrystal fracture in the microstructure. The size of columnar crystals decreases with the increase of the growth rate, increasing the number of grains and decreasing the orientation difference between the growth and axial directions as well as the preferred orientation of lamellar, and the anisotropy of the material, which leads to the obvious decrease of the tensile strength and plasticity. Combined with electron backscattering diffraction test results, the lamellar orientation of the effective parts of the three specimens after high temperature stretching was studied. It was found that the axial preferred orientation of the alloy specimens decreased obviously with the increase of the growth rate, and the orientation became disorderly and the uniformity of lamellar thickness decreased gradually with the increase of the growth rate. In addition, it was found that a new single-phase γ phase is formed in the microstructure after high temperature stretching, and the distribution range increased with the increase of the growth rate, which seriously degraded the axial preferred orientation of the alloy. It can be concluded that the directionally solidified alloy with a growth rate of 10 μm/s has better microstructure orientation and high temperature tensile properties.

This work studied Mo-TiC-xCr (x = 0.0, 0.5, 1.0 wt.%) matrix composites with different component gradients prepared by Spark Plasma Sintering (SPS). The high-temperature oxidation test was conducted at 1200 ℃ in the atmosphere to study the influence of Cr on the high-temperature oxidation behavior of TiC-reinforced Mo matrix composites. The phase composition and morphology of the oxide film were analyzed using X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS), and the goal was to determine the effect of the Cr content on the high-temperature oxidation properties of the Mo-TiC-xCr (x = 0.0, 0.5, 1.0 wt.%) matrix composites. The results showed that with increasing oxidation time, the oxide film on the surface of Mo alloy will crack and fall off easily, and the porosity gradually increases. Oxygen underwent vigorous oxidation through the pores and the inside of the matrix, and a protective MoO2 internal oxide film disappeared. With increasing Cr content, the high-temperature oxidation performance of the Mo alloy improved, the thickness of the oxide film decreased, warping of the surface oxide film was inhibited, the porosity decreased, and volatilization of MoO3 was inhibited. After oxidation, the surface oxide film was mainly composed of TiO2, MoO3, Cr2O3 and Cr2(MoO4)3 phases. The TiC particles dispersed in the matrix were oxidized to TiO2 to inhibit the oxidation of the alloy. The Cr formed a protective oxidation film of Cr2O3, which effectively reduced the porosity and delayed the volatilization of the MoO3, thus improving its oxidation performance.

In this paper, fracture morphology observation, microstructure analysis, standard corrosion test, and other experimental methods are used to analyze the causes of corrosion and cracking of steam turbine blades (0Cr19Ni9) produced by a certain company. The results showed that cracks appeared during the operation of the blade. A large number of dimples were observed under the scanning electron microscope, almost all of which were shear dimples; at the same time, fatigue bands were also distributed in them. The internal cause of the cracks is the long-term service, which causes the carbon and the alloy to undergo a diffusion reaction to form carbon-rich areas and carbides. They are thermally corroded in the service environment, and the carbon-rich zone is reduced, which reduces the strength of the zone; carbides accumulate at the grain boundary, causing groove-shaped defects at the grain boundary to form a cutting effect. It is easy to form a source of fatigue cracks. The external cause is that the material is subjected to transverse stress for a long time during operation, which leads to the generation of cracks. This article analyzes the failure causes of the blade and proposes related solutions, which have important reference value for production practice.

In this paper, the Titanium carbide/Molybdenum (TiC/Mo) alloy was prepared by spark plasma sintering (SPS). The oxidation process of the TiC/Mo alloy at different oxidation temperatures was studied, and the oxidation mechanism was discussed in depth. The focus is on the influence of the introduction of TiC particles on the high-temperature oxidation properties of Mo alloys. The phase composition and morphology of the oxide film were analyzed by means of X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS). The results showed that, after oxidation, the surface oxide film is mainly composed of Titanium dioxide (TiO2), Molybdenum dioxide (MoO2), Molybdenum trioxide (MoO3) and Molybdenum oxide hydrate (MoO3(H2O)2) phases. As the oxidation temperature increases, the surface of the oxide film will warp, and thereby increase porosity. The dense MoO2 will form a protective inner oxide layer and inhibit further progress of the TiC/Mo alloy. Oxygen will undergo violent oxidation through the pores and the inside of the matrix, and the protective MoO2 internal oxide film will disappear. TiC particles dispersed in the matrix will be oxidized to form TiO2, which will be gradually deposited on the surface of the oxide film, hindering the diffusion of oxygen to the matrix. The quantity loss during the entire oxidation process is significantly reduced. Therefore, the introduction of TiC can greatly improve the oxidation resistance of Mo alloys.

The research focuses on the high temperature oxidation resistance of martensitic heat-resistant steel. A new type of martensitic heat-resistant steel was developed with the addition of Al and Cu, and the oxidation behavior of the new martensitic heat-resistant steel at 650 °C and 700 °C was analyzed. The high temperature oxidation kinetics curves of new martensitic heat-resistant steel at 650 °C and 700 °C were determined and plotted by cyclic oxidation experiment and discontinuous weighing method. XRD technique was applied to qualitatively analyze the surface oxide of the material after oxidation. The surface and cross-section morphology of the material were observed by field emission scanning electron microscope (SEM) and energy dispersive spectrometer (EDS), and the oxidation mechanism at high temperature was analyzed. The results show that the oxide film can be divided into two layers after oxidation at 650 ºC for 200 h. The outer oxide film is mainly composed of Fe and Cu oxides, and the inner oxide film is mainly composed of Al2O3, SiO2 and Cr2O3. After oxidation at 700 ºC for 200 h, the outer layer is mainly composed of Fe, Cu, Mn oxides, and the inner layer is mainly composed of Cr, Al and Si oxides. The addition of a small amount of Cu promotes the diffusion of Al and Si elements, facilitates the formation of Al2O3 and SiO2, and improves the high-temperature oxidation resistance of martensitic heat-resistant steel.

A new type of hot working die steel was designed by using JMatPro, and high-temperature oxidation tests were carried out in the ambient atmosphere at 600 ℃ and 700 ℃. The heat treatment process and oxidation mechanism of the designed 4Cr4Mo2NiMnSiV steel were studied in detail. XRD, SEM and EDS were used to analyze the crystallographic phases, surface and cross-section morphologies of the oxide films. The results show that the main phases in the 4Cr4Mo2NiMnSiV steel were γ and α + δ. During the high-temperature oxidation, oxidation of the Fe outer layer and Cr inner layer occurred. After oxidation at 600℃, the surface oxidation layer comprised a monolayer with an uneven morphology. The surface oxide film had two layers after oxidation at 700℃. The outer oxide layer mainly contained Fe2O3 and Fe3O4, while the inner oxide layer mainly contained Cr2O3. The microstructure was relatively regular and had a significant effect on the protection of the metallic matrix. When oxidized, the 4Cr4Mo2NiMnSiV alloy steel easily formed protective layers, such as Cr2O3 and SiO2, so that the test steel had excellent oxidation resistance at high temperatures.

The research is focused on a novel aluminum and copper-containing heat-resistant steel. The steel was designed by the material performance simulation software JmatPro, performed high-temperature oxidation tests at 650 °C and 700 °C atmospheric conditions, and analyzed the high-temperature oxidation processes and its mechanisms.The phase transtions and surface morphology of the oxide films were studied using X-ray diffraction (XRD), electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS). The results showed that the equilibrium phase of the test steel is composed of γ phase and δ phase at 1050 °C and tranforms to tempered martensite and δ-Fe mixed structure after heat treatment. The preferential oxidation of Fe and Cr and the internal oxidation of Al occurred during the high temperature oxidation of the test steel. The oxide films were formed with various shape and weak bonding properties after high-temperature oxidation at 650℃. To the contrary, the oxide films more regular and evenly distributed, and has a certain protective effect after high-temperature oxidation at 700 ℃. The oxide films were divided into two layers, Fe2O3 is main element in the outer layer, the inner layer is mainly consisting the oxide of Cr. However, the addition of Cu element can promote the diffusion of Al and Si elements, which is beneficial to the formation of Al2O3 and SiO2 protective oxide films and excellent in high temperature oxidation resistance.