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在分析讨论铸铁性能参数的基础上,对常用的氧化参数——氧化增重及氧化层厚度的实验方法作了一些改进.经反复验证,认为采用改进的实验方法评价铸铁的氧化性能,可以得到比较精确的结果.最后还提出了新的氧化参数——氧化蚀掉深度的实验方法以及抗氧化性指标——氧化参数倒数的概念. 相似文献
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M. L. Zheludkevich A. G. Gusakov A. G. Voropaev A. A. Vecher K. A. Yasakau M. G. S. Ferreira 《Oxidation of Metals》2004,62(3-4):223-235
Kinetics of the oxidation of iron in fluxes of atomic and molecular oxygen have been studied over a wide temperature range from 573 to 1273 K. The influence of oxygen pre-dissociation on the oxidation rate was found negligible at 573–1073 K. At temperatures above 1073 K, when only FeO is formed, the rate of iron oxidation in atomic oxygen is substantially higher than that in molecular oxygen. Decarburization occurs during the first stage of oxidation of iron containing carbon. The rate of carbon elimination in atomic oxygen exceeds that in molecular oxygen due to the higher chemical potential of atomic gas. 相似文献
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《腐蚀工程科学与技术》2013,48(3):133-137
AbstractOxidation of (001), (011), (112)monocrystalline, and of large-grained and small-grained polycrystalline, pure Iron has been studied in laboratory air at room temperature at 44–46% relative humidity for 120 days by gravimetric methods, electron diffraction and electron microscopy. After the initial oxide growth, no significant oxidation occurred for about 20–30 days, when oxidation re-commenced slowly and became rapid, until after 90 days the rate became irregular and was associated with decreasing epitaxy. The rate of oxidation in decreasing order was(001), large grained, small grained, (011) and (112). Up to 70 days the outer layer was cubic Fe3O4 but after 90 days it was α-Fe2O3, probably with some γ-Fe2O3 and otherminor impurtties such as hydroxides. The influence of impurities on the oxide is emphasised by a weight loss of 5–7 % which occurred upon heating the specimens to 300° in vacuo after 120 days. γ-Fe2O3 and other minor impurities such as hydroxides. The influence of impurities on the oxide is emphasised by a weight loss of 5–7% which occurred upon heating the specimens to 300° in vacuo after 120 days. 相似文献
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Jan Matousek 《JOM Journal of the Minerals, Metals and Materials Society》2012,64(11):1314-1320
The state of oxidation of a pyrometallurgical process, given by the partial pressure of oxygen and the temperature, is one of the important properties monitored and controlled in the smelting and refining of iron and the nonferrous metals. This article reviews the thermodynamic background for this quantity and examines some empirical methods for its estimation and use. The emphasis is on copper smelting, but the same principles apply to iron, nickel, lead, and zinc processes. 相似文献
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V. A. Kotenev 《Protection of Metals》2003,39(4):301-310
The low-temperature passivation of the oxide growth on iron is studied with the use of digital ellipsometry at a temperature of 300°C and an oxygen pressure from 10–3 to 1 mmHg. The maximum increment in the oxide thickness as a function of the oxygen pressure P
a–p is observed in an hour of exposure, which indicates the active–passive transition. This passivity of iron and other metals can be caused by the multilayer and multiphase structure of the oxide film formed. As the oxygen pressure is increased, an external protective hematite layer appears on iron, and the inner quickly growing magnetite layer has no time to reach its limiting thickness. Shortening of the period of a rapid growth of magnetite, which is observed upon the increase in the oxygen pressure at the same exposure, results in the maximum of the summary thickness of the layer at a certain pressure P
a–p. Hematite over the magnetite layer is usually formed as laterally spreading islets, the coalescence of which sharply decelerates the oxidation. In the time–pressure–oxide thickness plot, the areas of the low-temperature passivation of iron can be distinguished in wide ranges of temperature and pressure. The electrophysical treatment in the range of the active–passive transition sharply intensifies the oxidation of iron-based alloys and leads to the formation of layers with a substantial thickness and protective ability. 相似文献
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The oxidation of pure iron with various oxygen contents was studied. Pure iron and ferrite containing different amounts of oxygen were oxidized for 1–5 hr in two types of oxidation atmospheres at 850°C. Pure iron (0.0037% oxygen) oxidized more rapidly than ferrite (0.017% oxygen). Oxidation is higher in the moist ambient atmosphere than in dry air. The oxidation rate was not proportional to the amount of oxygen in the samples. 相似文献
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J. W. Matousek 《JOM Journal of the Minerals, Metals and Materials Society》2013,65(11):1584-1588
The state of oxidation of a pyrometallurgical process given by the partial pressure of oxygen and the temperature (the oxidation potential) is one of the important properties monitored and controlled in the smelting and refining of iron and the nonferrous metals. Solid electrolyte sensors based on ZrO2 and a reference electrode such as Cr/Cr2O3 to measure the oxygen pressure found early application in the steel industry, followed soon after in copper, nickel, lead, and zinc smelting. Similar devices are installed in automobile postcombustion/exhaust trains as part of emission control systems. The current discussion reviews this technology as applied in the primary steps of iron and steel making and refining. 相似文献
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《腐蚀工程科学与技术》2013,48(4):216-220
AbstractA volumetric method has been used to study the kinetics of the initial oxidation of oure iron at two pressures of dry oxygen (viz. p O2 = 7·6 and 29 cm mercury) in the range 800–1000° in which the first allotropic transformation point of iron occurs. It was found that the oxidation of both body-centred cubic (b.c.c.) and face-centred cubic (f.c.c.)–iron at p O2 = 7·6 cm and of only b.c.c. at p O2 = 29 cm follows a modified parabolic law; a true parabolic law was found to operate in the oxidation of f.c.c.–iron only at p O2 = 29 cm. An anomaly, which is obtained in the Arrhenius plot at the allotropic change point of iron (~911°), is attributed to the effect of phase-boundary reactions on the oxidation kinetics. It would appear from the concept of vacancy distribution in iron, that for a modified parabolic law, it is the metal/oxide interfacial reaction in f.c.c.–iron and the oxide/oxygeninterfacial reaction in b.c.c.–iron that governs the phase-boundary controlled reaction rate. 相似文献
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微米级铁基纤维由Cu-11Fe-4Cr原位复合线材萃取得到。研究了在大气环境中加热对纤维样品结构和磁性的影响。采用X射线衍射和扫描电镜观察分析了样品的结构和形貌,采用振动样品磁强计测试了样品的磁性,利用热重-差热试验分析了纤维的热稳定性。结果表明,原始态纤维为铁素体结构,饱和磁化强度约为120A.m2.kg-1;在空气中600℃以下加热,纤维保持铁素体结构不变,经800℃以上加热后,由铁磁性的α-(Fe,Cr)固溶体转变为顺磁性的(Fe0.6Cr0.4)2O3,样品的饱和磁化强度显著下降。 相似文献
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The oxidation of Fe was investigated at 500–700°C in the presence of O2 with 0–1000 ppm SO2. The exposures were carried out in a thermobalance and lasted for 24 h. The oxidized samples were investigated by grazing-angle XRD, SEM/EDX, GDOES and XPS. The rate of oxidation of pure iron is slowed down by traces of O2 in O2 below 600°C while SO2 has no effect on oxidation rate at higher temperatures. Exposure to SO2<600°C resulted in the formation of small amounts of sulfate at the gas/oxide interface. In addition, sulfur, probably sulfide, accumulated at the metal/oxide interface. The influence of SO2 on oxidation rate is attributed to surface sulfate. The sulfur distribution in the scale is rationalized in terms of the thermodynamic stability of compounds in the Fe–O–S system. Exposure to SO2 caused the formation of hematite whiskers. 相似文献
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微米级铁基纤维的抗氧化性和磁性 总被引:1,自引:0,他引:1
微米级铁基纤维由Cu-11 Fe-4Cr原位复合线材萃取得到.研究了在大气环境中加热对纤维样品结构和磁性的影响.采用X射线衍射和扫描电镜观察分析了样品的结构和形貌,采用振动样品磁强计测试了样品的磁性,利用热重-差热试验分析了纤维的热稳定性.结果表明,原始态纤维为铁素体结构,饱和磁化强度约为120 A·m2·kg-1;在空气中600℃以下加热,纤维保持铁素体结构不变,经800℃以上加热后,由铁磁性的α-(Fe,Cr)固溶体转变为顺磁性的(Fe0.6 Cr0.4)2O3,样品的饱和磁化强度显著下降. 相似文献
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采用喂丝法球化处理,已在离心球墨铸铁管的大批量生产中得到应用,年处理球铁量达70多万吨。喂丝蠕化处理方法与喂丝球化处理方法相同。由于喂丝法有控制精确、改善劳动环境等优点,尤其可用计算机根据快速测定的硫量精确地控制喂丝量,因而能有效地控制蠕化质量。 相似文献