The development ofthe oxides on Fe-14%Cr-4%Al, Fe-27%Cr-4%Al, and similar alloys containing 0.008% Y, 0.023% Y, and 0.8% Y has been investigated during the early stages of oxidation in 1 atm oxygen at 1000 and 1200°C. In all cases, a steady-state -Al2O3layer is established rapidly, after some initial formation of transient oxides rich in iron and chromium. For the yttrium-free alloys the steady-state situation is achieved more rapidly for the higher chromium-containing alloy and at the higher temperature. The amount of transient oxide formed is also determined by the specimen surface topography since the development of the -Al2O3 layer is less rapid at the base of alloy asperities than at a flat alloy-oxide interface. Following establishment of the complete -Al2O3layer, the oxide develops a convoluted oxide morphology at temperature, due to high compressive growth stresses in the oxide. These arise following reaction between oxygen ions diffusing inward down the oxide grain boundaries and aluminum ions diffusing outward through the bulk oxide. This results in lateral growth of the oxide and plastic deformation and movement of the alloy in a direction parallel to the alloy-oxide interface. The addition of yttrium to the alloys promotes the selective oxidation of aluminum. Also, the yttrium is incorporated into the growing oxide where it changes the mechanism of growth, reducing the production of the high compressive growth stresses and thus the development of the convoluted oxide morphology. 相似文献
0IntroductionRecently,the development of bonding technique ofhigh temperature structure ceramic Si3N4becomes a hottopic in the field of ceramic bonding[1].Partial transientliquid phase bonding(PTLP)has been applied in the fieldof high temperature ceramic bonding and made some pro-gress.The selection of interlayer materials is key to PTLPbonding.Since Bender discovered that Ag-based brazingmaterial including Ti could wet ceramic in1954,morestudies have shown that Ti has good wetting prope… 相似文献
The brazing of Al2O3 to Nb was achieved by the method of transient liquid phase (TLP) bonding. Ti foil and Ni-5V alloy foil were used as interlayers for the bonding. The base materials were brazed at 1423-1573 K for 1-120 min. The results show that the shear strength of the joint first increases and then decreases with increasing holding time and brazing temperature. The joint interface microstructure and elements distribution were investigated. It can be concluded that a composite structure, in which the base metals are solid solution Nb(V) and Nb(Ti) reinforced by Ni3Ti, is formed when the brazing temperature is 1473 K and holding time 15 min, and a satisfactory joint strength can be achieved. The interaction of Ti foil and Ni-5V foil leads to the formation of liquid eutectic phase with low melting point, at the same time the combination of Ti come from the interlayer with O atoms from Al2O3 results in the bonding of Al2O3 and Nb. 相似文献
For the first time, the coupling of fast transient kinetic switching and the use of an isotopically labelled reactant (15NO) has allowed detailed analysis of the evolution of all the products and reactants involved in the regeneration of a NOx storage reduction (NSR) material. Using realistic regeneration times (ca. 1 s) for Pt, Rh and Pt/Rh-containing Ba/Al2O3 catalysts we have revealed an unexpected double peak in the evolution of nitrogen. The first peak occurred immediately on switching from lean to rich conditions, while the second peak started at the point at which the gases switched from rich to lean. The first evolution of nitrogen occurs as a result of the fast reaction between H2 and/or CO and NO on reduced Rh and/or Pt sites. The second N2 peak which occurs upon removal of the rich phase can be explained by reaction of stored ammonia with stored NOx, gas phase NOx or O2. The ammonia can be formed either by hydrolysis of isocyanates or by direct reaction of NO and H2.
The study highlights the importance of the relative rates of regeneration and storage in determining the overall performance of the catalysts. The performance of the monometallic 1.1%Rh/Ba/Al2O3 catalyst at 250 and 350 °C was found to be dependent on the rate of NOx storage, since the rate of regeneration was sufficient to remove the NOx stored in the lean phase. In contrast, for the monometallic 1.6%Pt/Ba/Al2O3 catalyst at 250 °C, the rate of regeneration was the determining factor with the result that the amount of NOx stored on the catalyst deteriorated from cycle to cycle until the amount of NOx stored in the lean phase matched the NOx reduced in the rich phase. On the basis of the ratio of exposed metal surface atoms to total Ba content, the monometallic 1.6%Pt/Ba/Al2O3 catalyst outperformed the Rh-containing catalysts at 250 and 350 °C even when CO was used as a reductant. 相似文献
Electron-beam irradiated GaN n+-p diodes were characterized by deep level transient spectroscopy (DLTS) and optical responsivity measurements. The GaN n+-p diode structures were grown by metal organic chemical vapor deposition technique, and the electron irradiation was done by the energies of 1 MeV and 2 MeV with dose of 1 × 1016 cm− 2. In DLTS measurement, the defect states of Ec − 0.36 eV and Ec − 0.44 eV in the electron irradiated diodes appeared newly. The optical responsivity of GaN n+-p diode was characterized in ultra-violet region, and then the maximum optical responsivity at 350 nm was decreased after electron-beam irradiation. 相似文献