Friction and wear behaviors of Nb-Ti-Si-Cr based ultrahigh temperature alloy and its Zr-Y jointly modified silicide coatings

Zr-Y jointly modified silicide coatings were prepared on an Nb-Ti-Si-Cr based ultrahigh temperature alloy by pack cementation process. The wear behaviors of both the base alloy and coatings were comparatively studied at room temperature and 800 ℃ using SiC balls as the counterpart. The Zr-Y jointly modified silicide coating is mainly composed of a thick （Nb,X）Si2 outer layer and a thin （Ti,Nb）5Si4 inner layer. The coatings possess much higher microhardness than the base alloy. The wear rates of both the base alloy and coatings increase with increasing the sliding loads. However, the coatings have much lower wear rates than the base alloy under the same sliding conditions. The coatings have superior anti-friction property, and can provide effective protection for the base alloy at both room temperature and 800 ℃ in air.

Microstructure and hot corrosion behavior of Al-Ce-Y coatings on DZ125 nickel-based alloy prepared by pack cementation process

In order to improve the hot corrosion resistance of DZ125 alloy,Ce-Y modified aluminum coatings were prepared on DZ125 alloy by pack cementation process at 950°C for 2 h.The microstructure,phase constitution and formation mechanism of the coatings were investigated.The hot corrosion behaviors of DZ125 alloy and the coatings in molten salt environment of 25%K2SO4+75%Na2SO4(mass fraction)at 900°C were studied.Results show that the obtained Al-Ce-Y coatings were mainly composed of Al3Ni2,Al3Ni and Cr7Ni3,with a thickness of about 120μm.After hot corrosion test,DZ125 alloy suffered catastrophic hot corrosion and serious internal oxidation and internal sulfidation arose.Two layers of corrosion products formed on surfaces of DZ125 alloy,including the outer layer consisting of Cr2O3 and NiCr2O4,and the inner layer of Al2O3,Ni3S2 and Ni-base solid solution.After being coated with Al-Ce-Y coating,the hot corrosion resistance of DZ125 alloy is improved notably,due to the formation of a dense scale mainly consisting of Al-rich Al2O3 in the coating layer.

Zirconium Modified Aluminide Coatings Obtained by the CVD and PVD Methods

The paper presents the comparison of the structures of the zirconium modified aluminide coatings deposited on pure nickel by the CVD and PVD methods. In the CVD process, zirconium was deposited from the ZrCl3 gas phase at the 1000°C. Zirconium thin layer (1 or 7 μm thick) and aluminum thin layer (1.0, 0.7 or 0.5 μm thick) were deposited by the EB-PVD method. Deposition velocity was about 1 ?m/min. The layers obtained by the Electron Beam Evaporation method were subjected to diffusion treatment for 2 h in the argon atmosphere. The obtained coatings were examined by the use of an optical microscope (microstructure and coating thickness) a scanning electron microscope (chemical composition on the cross-section of the modified aluminide coating) and XRD phase analysis. Microstructures and phase compositions of coatings obtained by different methods differ significantly. NiAl(Zr), Ni3Al and Ni(Al) phases were found in the CVD aluminide coatings, whereas Ni5Zr, Ni7Zr2 and γNi(Al,Zr) were observed in coatings obtained by the PVD method. The results indicate that the microstructure of the coating is strongly influenced by the method of manufacturing.