The isothermal oxidizing kinetics of Co-40Cr alloy and its yttrium ion-implanted samples are studied at 1 000 ℃ in air by thermal-gravity analysis （TGA）. Scanning electronic microscopy （SEM） is used to examine the Cr2O3 oxide film＇s morphology after oxidation. Acoustic emission （AE） method is used in situ for monitoring the cracking and spalling of oxide films formed on both samples during oxidizing and subsequent air-cooling stages. Theoretical model is proposed relating to the film fracture process and is used for analyzing the acoustic emission spectrum both on time domain and on AE-event number domain. It is found that yttrium implantation remarkably reduces the isothermal oxidizing rate of Co-40Cr and improves the anti-cracking and anti-spalling properties of Cr2O3 oxide film. The reasons for the improvement are mainly that the implanted yttrium reduced the grain size of Cr2O3 oxide, increased the high temperature plasticity of oxide film, and remarkably reduced the number and size of Cr2O3/Co-40Cr inteffacial defects.
The influence of rare earth chloride LaCl3 ·7H2O addition on the microstructural features, phase structure, corrosion resistance and microhardness of nickel-electroplating was investigated. The Watts-type with different additive amounts of LaCl3·7H2O（0-1.2g/L） were used in the experiment. Surface morphologies of coatings were examined by scanning electronic microscopy （SEM）, transmission electronic microscopy （TEM） was used to measure the coatings＇ grain size and the microstructure of coatings was detected by X-ray diffraction （XRD）. Corrosive investigation was carried out in 3.5 wt.% NaCl solution. The microhardness values of the coatings with different amounts of LaCl 3·7H2O were measured, and the mechanism of the variation in microhardness was studied. Results showed that the addition of rare earth lanthanum refined the grain size and improved the surface consistency of the coatings, meanwhile the microhardness and corrosion property of coatings were improved and achieved a maximum with arround 1.0g/L LaCl 3·7H2O addition in electrolyte. The preferred growth orientation of lanthanum doped coating was crystal face （200）, meanwhile the La2 Ni7 phase was detected in the nickel coating by XRD and this was due to the induced co-deposition of elements La and Ni. The reason maybe was that the special out-layer electronic structure of element La raised the polarization of Ni cathode deposition, accelerated the nucleation of Ni and reduced hydrogen evolution from cathode surface.
Electroless Ni-P/nano-CeO2 composite coating was prepared in acidic condition, and its microstructure and corrosive property were compared with its CeO2-free counterpart.Scanning electronic microscopy（SEM）, transmission electronic microscopy（TEM）, X-ray diffraction spectrometer（XRD）, and differential scanning calorimeter（DSC） were used to examine surface morphology and microstructure of the coating.Corrosive investigation was carried out in 3%NaCl＋5%H2SO4 solution.The results showed that Ni-P coating had partial amorphous structure mixed with nanocrystals, whereas the Ni-P/CeO2 coating had perfect amorphous structure.In high temperature condition, Ni3P precipitation and Ni crystallization occurred in both coatings but at different temperatures, whereas the Ni-P/CeO2 coating had sintered phase of NiCe2O4 spinels.The anticorrosion property and passivity were improved in the CeO2-containing coating due to its less liability to undergo local-cell corrosion than its CeO2-free counterpart.During the co-deposition process, some Cen＋（n=3, 4） ions may be adsorbed to the metal/solution interface, hinder nickel＇s crystal-typed deposition and promote phosphorous deposition.The nano-CeO2 doping finally resulted in the coating＇ perfect amorphous structure and good anti-corrosive property.
Isothermal oxidation behavior of chromium with and without nanometric sol-gel CeO2 coating is studied at 1000℃ in air. Scanning electron microscopy （SEM） and transmission electron microscopy （TEM） are used to examine the surface morphology and microstructure of their oxide films. It is found that ceria coating greatly improves the anti-oxidation property of chromium. Laser Raman spectrometer and X-ray diffraction spectrometer （XRD） are also used to study the stress level in oxide films formed on ceria-coated and ceria-free Cr. The difference in oxidation behavior is mainly attributed to the fact that ceria greatly reduces the growth speed and grain size of Cr2O3 film, and this fine grain-sized Cr2O3 film probably has better high temperature plasticity, i.e. oxide film can relieve parts of compressive stress by means of creeping. XRD and Raman testing results both show the stress declination due to nano-CeO2 application, and their deviation is analyzed conceming to the rare earth effect.
Isothermal and cyclic oxidizing behavior of Co-40Cr alloy and its lanthanum ion-implanted samples were studied at 1000 ℃ in the air by thermal-gravimetric analysis （TGA）. Scanning electronic microscopy （SEM） and transmission electronic microscopy （TEM） were used to examine the morphology and structure of oxide film after oxidation. Secondary ion mass spectrum （SIMS） method was used to examine the binding energy change of chromium caused by La-doping and its influence on the formation of Cr2O3 film. laser Raman spectrum was used to examine the stress changes within the oxide film. It was found that lanthanum implantation remarkably reduced isothermal oxidizing rate of Co-40Cr and improved anti-cracking and anti-spalling properties of Cr2O3 oxide film. The reasons for the improvement were mainly that the implanted lanthanum reduced the grain size and internal stress of Cr2O3 oxide and increased high temperature plasticity of the oxide film. Lanthanum mainly existed on the outer surface of Cr2O3 oxide film in the form of fine La2O3 and LaCrO3 spinel particles.
Electroless Ni-P/nano-CeO2 composite coating was prepared in acidic condition, and its microstructure and corrosive property were compared with its CeO2-free counterpart. Scanning electronic microscopy （SEM） and X-ray diffraction （XRD） spectrometer were used to examine surface morphology and structure of the as-plated coating. Differential scanning calorimeter （DSC） and transmission electronic microscopy （TEM） were used to study the coating＇s phase change at high temperature. The coating＇s corrosive behavior in 3%NaCl ＋ 5%H2SO4 solution was also investigated. The results showed that Ni-P coating had partial amorphous structure mixed with nano-crystals, while the Ni-P/CeO2 coating had perfect amorphous structure. In high-temperature condition, Ni3P precipitation and Ni crystallization took place in both coatings but at different temperatures, while the Ni-P/CeO2 coating had sintered phase of NiCe2O4 spinels. The anti-corrosion property was better in the CeO2-containing coating, and this was due to its less liability to undergo local-cell corrosion than its CeO2-free counterpart. Ni-P/CeO2 coating＇s pure amorphous structure was the result of Ni＇s hindered crystal-typed deposition and P＇s promoted deposition.
