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Atomic-scale oxidation dynamics of Cu2O nanocrystallines （NCs） are directly observed by in situ high-resolution transmission electron microscopy. A two-stage oxidation process is observed： （1）The initial oxidation stage is dominated by the dislocation-mediated oxidation behavior of Cu2O NCs via solid-solid transformations, leading to the formation of a new intermediate CuOx phase. The possible crystal structure of the CuOx phase is discussed. （2） Subsequently, CuOx is transformed into CuO by layer-by-layer oxidation. These results will help in understanding the oxidation mechanisms of copper oxides and pave the way for improving their structural diversity and exploiting their potential industrial applications.

The non-isothermal oxidation experiments of ilmenite concentrate were carried out at various heating rates under air atmosphere by thermogravimetry.The oxidation kinetic model function and kinetic parameters of apparent activation energy（Ea）were evaluated by Málek and Starink methods.The results show that under air atmosphere,the oxidation process of ilmenite concentrate is composed of three stages,and the chemical reaction（G（α）=1-（1-α）~2,whereαis the conversion degree）plays an important role in the whole oxidation process.At the first stage（α=0.05-0.30）,the oxidation process is controlled gradually by secondary chemical reaction with increasing conversion degree.At the second stage（α=0.30-0.50）,the oxidation process is completely controlled by the secondary chemical reaction（G（α）=1-（1-α）~2）.At the third stage（α=0.50-0.95）,the secondary chemical reaction weakens gradually with increasing conversion degree,and the oxidation process is controlled gradually by a variety of functions;the kinetic equations are G（α）=（1-α）~（-1）（β=10K·min~（-1）,whereβis heating rate）,G（α）=（1-α）~（-1/2）（β=15-20K·min~（-1））,and G（α）=（1-α）~（-2）（β=25K·min~（-1））,respectively.For the whole oxidation process,the activation energies follow a parabolic law with increasing conversion degree,and the average activation energy is 160.56kJ·mol~（-1）.

The oxidation kinetics and composition of oxide scales on low carbon steel （SPHC） were studied during i- sothermal oxidation. Thermogravimetric analyzer （TGA） was used to simulate isothermal oxidation process of SPHC for 240 min under air condition, and the temperature range was from 500 to 900 ℃. Scanning electron microscope （SEM） was used to observe cross-sectional scale morphology and analyze composition distribution of oxide scales. The morphology of oxide scale was classical three-layer structure. Fe2 03 developed as whiskers at the outermost lay- er, and interlayer was perforated-plate Fe3 04 while innermost layer was pyramidal FeO. From the oxidation curves, the oxidation mass gain per unit area with time was of parabolic relation and oxidation rate slowed down. On the ba- sis of experimental data, the isothermal oxidation kinetics model was derived and oxidation activation energy of SPHC steel was 127. 416 kJ/mol calculated from kinetics data.

Simultaneous thermal analysis（STA） was used to investigate the effects of silicon content on the oxidation kinetics of silicon-containing steels under an atmosphere and heating procedures similar to those used in industrial reheating furnaces for the production of hot-rolled strips. Our results show that when the heating temperature was greater than the melting point of Fe2SiO4, the oxidation rates of steels with different silicon contents were the same; the total mass gain decreased with increasing silicon content, whereas it increased with increasing oxygen content. The oxidation rates for steels with different silicon contents were constant with respect to time under isothermal conditions. In addition, the starting oxidation temperature, the intense oxidation temperature, and the finishing oxidation temperature increased with increasing silicon content; the intense oxidation temperature had no correlation with the melting of Fe2SiO4. Moreover, the silicon distributed in two forms： as Fe2SiO4 at the interface between the innermost layer of oxide scale and the iron matrix, and as particles containing silicon in grains and grain boundaries in the iron matrix.

The isothermal oxidation behavior of a new Refree nickel-based single-crystal superalloy in air at 950 ℃ for 200 h was studied by scanning electron microscopy（SEM）with energy-dispersive spectroscopy（EDS）and X-ray diffraction（XRD）.The results indicate that oxidation kinetics obeys parabolic law approximately,and the mass gain increases rapidly during initial oxidation stage and then gradually slows down.The oxidation scales are composed of three layers：the outer layer mainly consists of NiO with a small amount of CoO;the intermediate layer is mainly composed of Cr_2O_3 with a small amount of spinel compounds such as CrTaO_4,NiCr_2O_4,CoCrAl_2O_4,CoAl_2O_4,and NiAl_2O_4;and the inner layer is composed of Al_2O_3.Inner Al_2O_3 layer suppresses the diffusion of elements between oxygen and alloy elements,slows down the alloy oxidation speed,and also suppresses the growth of the oxide scale and reduces the oxidation rate,which is agreeable with the oxidation kinetics.

The oxidation morphologies of modified 310 steel exposed in 900 and 1 100 ℃ air were investigated. A double layer morphology consisting of a （Cr, Mn）-rich outer layer and a fine Cr-rich inner layer was formed at 900℃. It was related to the breakaway oxidation induced by the Cr-depletion and the Mn-segregation in inner layer. Some Cr-rich oxides with amorphous state were formed along grain boundaries. And some new finer oxide grains, voids and Cr-rich precipitates were observed in spallation areas at 1 100℃. Correspondingly, the oxidation kinetic curve dropped with the spallation of scale and increased with the formation of some new oxide grains. It was caused by segregation of Cr and the transformation of oxides from Cr2O3 to the volatile oxides at elevated temperature. XRD analysis showed that the precipitates were mainly composed of CrO3. Segregation and depletion for solutions were also discussed by oxidation diffusion mechanisms.

The sphalerite oxidative kinetics under hypergene condition was simulated and studied by means of a mixed flow reactor over a pH range of 1.0-7.8, and at dissolution temperatures from 20 to 55℃, ferric ion concen- trations from 1.0×10^-5 to 1.0×10^2mol/L, 02 flux of 0.5 L/min, and oxidants of ferric ion and 02. It is indicated that with ferric ion as oxidant, the oxidation rate of sphalerite increases with increasing ferric ion concentration, tem- perature and decreasing pH value, and under the studied conditions, the dissolution rates of Zn and Cd are approxi- mately identical, with the values of activation energy being 41.75 and 42.51 kJ.mol-~, respectively, suggesting that the oxidation rate of sphalerite is controlled by chemical reactions on mineral surface. However, with 02 as oxidant, the oxidation mechanism of sphalerite varies with pH value. Oxidation rate decreases with increasing pH value when pH is lower than 5.95, whereas the increase of pH value results in an increase in oxidation rate when pH value is higher than 7. The oxidation rate of sphalerite can be expressed as：

The kinetic curve of the high-temperature oxidation of austenitie stainless steel Crl8Ni11 Cu3Al3MnNb at different temperatures was measured by weighting method. It is showed that the oxidation curves at 700 and 800 ℃ followed the parabolic law, and the steel presented an excellent anti-oxidation. The surface morphology and structure of the oxide film were studied by scanning electron microscopy and X-ray diffraction methods. A dense oxide film was attained at 700 and 800 ℃, mainly composed of the hexagonal Al2 O3, Fe2 O3, and a small amount oxide of Cr at 700 ℃. At 900 ℃ the oxide film started to delaminate, and was composed of （Cr,Fe）2O3 and the spinel CuCrMnO4 and Fe（Cr, Al） 2O3.

By oxidation weight gain method, four groups of Fe-based superalloys with different content of chromium, aluminium and silicon were tested at 1 200 ℃ for 500 hours. According to the oxidation weight gains, the oxidation kinetic curves were plotted, and the equations were regressed by least square method and non-linear curve fitting. The effects of different scale compositions on the morphology and oxidation kinetic law were studied further by analysis of X-ray diffraction （XRD） and scanning electron microscope （SEM）. It is found that the compounded scale is composed of Cr2O3, Al2O3, SiO2 and FeCr2O4, with compact structure and fine grains, possessing complete oxidation resistance at 1 200 ℃, and the oxidation kinetic curve follows the power function of y=axb （a0, 0b1）. When the compounded scale lacks Al2O3 or SiO2, it becomes weak in oxidation resistance, but the oxidation kinetic curve still follows the power function with bigger parameter b. When Cr2O3 is absent, the kinetic curve shows two parts： the slow adding of oxidation weight gains at the beginning and the ascending line in the end. Such scale loses oxidation resistance completely.