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1.
High temperature oxidation of metals leads to residual stresses in the metal and in the oxide. In this work, we try to predict the evolution of the residual stresses in the growing oxides layers, during isothermal oxidation. The origin of these stresses is based on the microstructural model of Clarke, however, another justification is proposed, assuming a proportional dependence of the growth strain with the oxide layer thickness. Using the mechanics of thin layers, as well as the analysis proposed to describe the growth strain, a system of equations are deduced that predict the stresses evolution with oxidation time. Numerical analysis is performed, leading to a set of theoretical curves.  相似文献   

2.
In this present work, local stress development in the iron oxide layers growing on phosphated α-Fe at 400 °C in ambient air is investigated by Raman spectroscopy. Coupled with X-ray diffraction it enables to obtain directly local stresses’ maps in the oxide layers. Use of Raman spectroscopy allows obtaining better accuracy on mechanical behaviour at local scale. This characterisation technique is very useful to study systems developing mechanical heterogeneities on surface, especially in case of buckling phenomenon. Investigations on particular local blisters have been done to measure some characteristic lengths at local scale. From local measurements, we are able to evaluate general effect of buckling from simplified scale transition. So, a macroscopic approach has been performed to calculate global stress evolution of the oxide layer, based on continuous damage mechanics. Consequently, it leads to good comparison between modelling and experimental values (global stresses versus oxidation time) in α-Fe2O3 oxide.  相似文献   

3.
A continuum model is proposed to describe the process of scanned probe oxidation in the presence of a thin water layer on the surface of a substrate. The model describes the electric field and ion transport in both the liquid and the oxide layers and incorporates the reaction mechanism at the substrate/oxide interface. Further, the influence of the space charge due to ions trapped near the substrate/oxide interface is taken into account.Separation of time scales for the chemical reactions and ion transport as well as the asymptotic limit in terms of a small aspect ratio of the oxide layer are used to reduce the complex system of partial differential equations to a one-dimensional system of ordinary differential equations. The analytical solution of the reduced system results in the evolution equation for the oxide thickness. Numerical simulations of the evolution equation predict features of oxide growth that qualitatively agree with the experimental observations. A parametric study is conducted to determine the influence of the key operating and material parameters on the thickness of the oxide, the electric field, and ion concentration in the system.  相似文献   

4.
An axisymmetric continuum model for oxide growth by the scanned probe oxidation technique is presented. The model includes equations describing the electric fields, hydroxyl and hydrogen ion concentrations, and oxide free boundaries defining the system. The governing system of partial differential equations tracks ion transport in the liquid and oxide layers and includes reactions at the substrate/oxide interface. Further, space charge effects are considered near the substrate/oxide interface. Two liquid configurations, semi-infinite layer and hemispherical drop of liquid, are examined to determine the potential in the liquid region. The AFM tip is modeled as either a point or a ring source of charges. The asymptotic limit of a small aspect ratio (height to width) oxide feature is used to reduce the governing equations to a quasi-one-dimensional system to determine the ion transport. The solution of the reduced system leads to an evolution equation for the oxide thickness and radius. Numerical simulations of the evolution equation predict oxide features that qualitatively agree with experimental observations. A parametric study is conducted to determine the influence of key operating and material parameters on the thickness and radius of the oxide, and the electric and ion concentration fields in the system.  相似文献   

5.
Sm2Fe17N3 sintered compacts were prepared below 450 °C by a high-pressure current sintering technique. The coercivity of the sintered compacts decreased linearly as the sintering temperature increased. Transmission electron microscopic analyses indicated that thin Fe-rich layers containing α-Fe phases were formed just inside the initial oxide layer on the particle surfaces and interfaces in the sintered samples. The generation of α-Fe phases was supposed to cause the coercivity decrease. In addition, X-ray photoelectron spectroscopy analysis revealed that Fe2O3 and FeO contained in the oxide layer of the raw powder disappeared subsequent to heat treatment. These results suggested that the α-Fe phases were generated by the oxidation–reduction reaction between the initial iron oxides and the primary Sm2Fe17N3 phase but not by thermal decomposition or exogenous oxidation during sintering. This mechanism was supported by the fact that extending the sintering time did not result in any further decrease in the coercivity.  相似文献   

6.
卢豫曾  郑耀宗 《物理学报》1985,34(4):447-454
本文中提出了一个同时适用于描述极薄及厚二氧化硅层生长规律的新的氧化模型。该模型假定在氧化过程中,二氧化硅层内的总净电荷具有指数分布。本文考虑了此氧化层电荷的影响,并推得了硅热氧化的新关系式。此新关系式不论是对非常薄或厚氧化层都与实验结果符合得很好。对于厚氧化层此式则过渡到熟知的Deal-Grove关系。利用本模型还可满意地解释外加电场对氧化速率的影响。 关键词:  相似文献   

7.
Biofunctional coatings are necessary to improve integration of titanium implants in the host tissue but they may be detrimental for the implant fatigue properties. This study presents an attempt towards enhancement of the in vitro fatigue strength of plasma electrolytic oxidation coated Ti6Al4V alloy by applying shot peening process prior to coating. The electrolytic oxidation was performed in calcium acetate and calcium glycerophosphate electrolytes that allowed formation of porous oxide coatings with high surface free energy and apatite like ability. A deformed surface layer coupled with induced residual compressive stresses seem to affect oxide growth rate and fatigue behavior of the titanium alloy.  相似文献   

8.
We have measured the oxidation rate of tungsten and the evaporation rate of tungsten oxide in the temperature range from 900 to 1200 K at an oxygen pressure from 5 × 10?4 to 5 × 10?3 Torr. The oxidation rate increases steadily with coverage in the whole range studied. The evaporation rate decreases at high pressure and is strongly dependent on the initial conditions of the experiments. These kinetic measurements support a qualitative model of oxidation. The surface is composed of oxide islands surrounded by oxide-free regions covered only by chemisorbed oxygen atoms. On the bare regions beside the chemisorbed oxygen atoms we suppose the existence of a dilute chemisorbed oxide layer which can either enter the condensed oxide phase or evaporate. The number of the growing islands is set up at the beginning of the reaction and does not increase further. This model, consistent with kinetic results during oxidation, has been proposed first to explain results obtained by Auger electron spectroscopy and thermal desorption spectroscopy under vacuum. Faceting is particularly important in the early stages of the experiment because it can hinder the nucleation of the oxide which is a necessary step for growth. In a narrow range of temperature and oxygen pressure this inhibited nucleation leads to an enhanced evaporation rate so that the growth rate is lower. Recording this growth rate allows us to follow faceting. The parameters studied are the oxygen coverage and the temperature, experimental results are in agreement with LEED and RHEED results. Reconstruction and faceting are discussed and are believed to be caused by a smoothing of the surface during the chemisorption step.  相似文献   

9.
Iron oxide nanoclusters have been prepared by the gas-phase aggregation technique to form thin film structures with very high exchange bias values (up to 3000?Oe at low temperatures). Composition has been analysed by x-ray absorption and M?ssbauer spectroscopies in order to elucidate the actual origin of the observed magnetic behaviour. The formation of a metal-oxide core-shell arrangement to explain the observed exchange bias has to be discarded since results show no metallic iron content and the main presence of α-Fe(2)O(3). The observed weak ferromagnetism and exchange bias are in agreement with the obtained size of α-Fe(2)O(3) nanoparticles: weak ferromagnetism because of the well-known spin canting in this antiferromagnetic structure and exchange bias because of the interaction between different spin sublattice configurations promoted by the modification of iron coordination in α-Fe(2)O(3) nanoparticles. Moreover, the preparation method is proposed for tuning both magnetization and exchange bias values by modification of the preparation conditions of α-Fe(2)O(3) nanoparticles, which open new possibilities in the design of new materials with required properties.  相似文献   

10.
TiO_2对α-Fe_2O_3纳米微粒拉曼散射效应的影响   总被引:2,自引:2,他引:0  
选取α Fe2O3和TiO2研究一种氧化物对另一种氧化物的拉曼散射效应。采用Sol gel方法制备纳米α Fe2O3/TiO2复合微粒,α Fe2O3粒径及含量分别为20nm、150nm和3%、6%、12%。制备过程中调节水解时的pH值和热处理温度,得到掺杂α Fe2O3粒子的不同晶型的TiO2纳米颗粒。Raman测量结果显示,α Fe2O3粒径越小、含量越高,TiO2对其散射效应的影响越大。不同的TiO2晶型对α Fe2O3纳米粒子的拉曼增强效应也不同。锐钛矿型及金红石型TiO2对α Fe2O3有一定的拉曼增强作用,当水解pH值较小时,得到板钛矿型TiO2,由于部分板钛矿型TiO2振动声子模的峰位与α Fe2O3的重叠,所以尚难观察它对α Fe2O3的拉曼增强效应。  相似文献   

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