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1.
K. Yanada M. Sakairi T. Kikuchi Y. Oya Y. Kojima 《Surface and interface analysis : SIA》2010,42(4):189-193
An in situ artificial micro‐pit fabrication method with an area selective electrochemical measurement technique was applied to investigate the effect of the geometry of artificially formed pits on their localized corrosion behavior in anodized 1000 series aluminum. This technique enables the fabrication of artificial micro‐pits with different aspect ratios (pit depth/pit diameter) in solutions. The aspect ratios of the fabricated artificial micro‐pits in this experiment could be varied from 0.13 to 1.83 by controlling the irradiation time of the focused pulsed YAG laser beam. By applying a constant potential to the final laser‐beam‐irradiated spot in chloride environments, localized dissolution occurred only at the laser beam irradiated area, because the anodic oxide film acted as an insulator. The corrosion current and charge increase with increasing aspect ratio at any applied potential. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
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A.?D.?DavydovEmail author V.?S.?Shaldaev A.?N.?Malofeeva L.?V.?Kasparova 《Russian Journal of Electrochemistry》2005,41(10):1032-1037
Anodic potentiodynamic and chronoamperometric curves on nickel-chromium alloys (2–50 wt % Cr) are obtained in NaCl solutions at various concentration, pH, and temperature. The dependences of pitting and repassivation potentials on the concentration and temperature are determined for alloy with 20 wt % Cr. The effect of the Cr content and pH on the anodic behavior of the alloys, in particular, the transition from a pitting breakdown of passivity to transpassivation, is shown. Quantitative time dependences of the current in the passive range are obtained and the steady-state values of this current are determined. The corrosion potential of the alloy with 20 wt % Cr is measured. Cathodic voltamograms for passive and chloride-ion-activated surface of the alloy are obtained. 相似文献
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Corrosion resistances of passive films on low‐Cr steel and carbon steel in simulated concrete pore solution 下载免费PDF全文
Ming Liu Xuequn Cheng Gucheng Zhao Xiaogang Li Yue Pan 《Surface and interface analysis : SIA》2016,48(9):981-989
The passive ranges of carbon steel rebar and 3Cr steel rebar in saturated Ca(OH)2‐simulated concrete pore solution with pH 12.6 were determined by means of cyclic voltammetry and potentiodynamic polarization curves. Chronopotentiometry was used to obtain steady‐state conditions for the formation of passive films on rebar samples at different anodic potentials. Electrochemical impedance spectroscopy, Mott–Schottky and X‐ray photoelectron spectrometer curves were employed to compare the formed passive films at different potentials. Additionally, cyclic polarization curves were used to compare the corrosion resistances of formed passive films on the two rebars in saturated Ca(OH)2‐simulated concrete pore solution with different concentration of Cl?. The results show that the passive ranges of the two rebars are all between ?0.15 and +0.6 V, and more stable passive films can be formed on both rebars at the anodic potential of +0.3 V. In the absence of Cl?, the stability and corrosion resistance of the passive film formed on the 3Cr rebar are better than those of CS rebar. The passive film of 3Cr steel has the relatively better pitting corrosion resistance than carbon steel in saturated Ca(OH)2‐simulated concrete pore solution that contains different concentration of Cl?. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
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Traditional researches on metal corrosion under salt solutions deposit conditions are usually carried out by visual, electron microscopic observations and simple electrochemical measurement via a traditional one-piece electrode. These techniques have difficulties in measuring localized corrosion that frequently occur in inhomogeneous media. This paper reports the results from the experiments using specially shaped coupons and a relatively new method of measuring heterogeneous electrochemical processes, namely, the wire beam electrode(WBE). Preliminary results from copper and aluminum corrosion in highly concentrated sodium chloride solutions with and without solid deposits show that the method is useful in simulating and studying corrosion especially localized corrosion in pipelines. 相似文献
6.
用动电位和恒电位极化法研究了A3碳钢在NaNO2_NaCl溶液体系中的电流波动特征.A3钢在不含Cl-的0.1mol/LNaNO2溶液中能保持良好的钝态,当加入一定浓度的Cl-后,电流出现了明显的快速上升,再缓慢下降的波动特征,表明此时碳钢表面生成了溶解较快而再钝化相对较慢的亚稳态孔蚀.实验中可观察到因电流波动而产生的累积腐蚀损伤的蚀孔.实验表明,随着Cl-浓度的增加,出现亚稳态孔蚀的初始电位Em降低,相应的电流波动峰值增大,峰频增加;而升高电位,则电流波动的峰值和峰频也都增加,况且再钝化时间延长,由此可见电位的升高促进了亚稳态孔的溶解,并能激活更多的活性点使孔诱发速率增大. 相似文献
7.
Molybdenum ions are implanted into aluminium with high ion flux and high dose at elevated temperatures of 200℃, 400℃ and 500℃. Due to the high temperature and high flux of vacancies and interstitial atoms, the atom diffusion and chemical effects are enhanced during the ion implantation. The effects increase with increasing ion flux and dose, so that new phase formation and phase transition emerge noticeably. X-ray diffraction analysis shows that when the aluminium is implanted with Mo ions at a low ion flux (25μA/cm2), the Al5Mo alloy is formed. The atomic ratio of Mo/Al of the Al5Mo phase is close to 20%. When the aluminium is implanted with Mo ions at a high ion flux (50μA/cm2), the phase transition from Al5Mo to Al12Mo appears, and the latter is dominant, which is determined to be the final phase. The ratio of Mo/Al in Al12Mo is 7.7%. Rutherford backscattering spectroscopy indicates also that the Mo/Al atom ratio is ~7% to ~8% in Mo-implanted aluminium. The atomic ratios of the constituents in Al5Mo and Al12Mo are of stoichiometric composition for these alloys. The thicknesses of the Al12Mo alloy layers for Mo-implanted Al with ion doses of 3×1017/cm2 and 1×1018/cm2 are 550nm and 2000nm, respectively. The pitting corrosion potential Vp increases obviously. It is clear that due to the formation of Al12Mo alloy layer, the pitting corrosion resistance is enhanced. 相似文献
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Surface films on metals and alloys often protect them from reaction with the environment, and hence a knowledge of their protective
properties and composition could be invaluable for predicting their corrosion behaviour. XPS (x-ray photoelectron spectroscopy)
could provide a quantitative analysis of the chemical composition, the nature of valence states and elemental distribution
within the surface films.
The present paper reviews the potential of this technique in corrosion studies. A brief review of the work done on the passivation
of iron and iron-chromium alloys and on the inhibition studies on copper base alloys has been given. A few examples of investigations
carried out at authors’ laboratory are also included. An attempt has been made to establish a correlation between the compositions
of the films formed and corrosion behaviour of carbon steel in 10.5 pH lithium hydroxide solution and of Cu-Ni alloys and
sacrificial Al-Zn-Sn alloys in synthetic sea-water. 相似文献
9.
Marina Cabrini Sergio Lorenzi Tommaso Pastore Cristian Testa Diego Manfredi Giulio Cattano Flaviana Calignano 《Surface and interface analysis : SIA》2019,51(12):1159-1164
The paper deals with the corrosion resistance in chloride solutions of an AlSi10Mg alloy obtained by laser powder bed fusion (LPBF) process. The potentiodynamic tests were carried out in solutions having different chloride contents. The results emphasize the role of chloride concentration on localized corrosion. The increase of concentration reduces pitting potential. In addition, the influence of the post-processing heat treatment temperature was recognized. Penetrating attacks occurred either on after low temperatures stress relieving or specimens without any treatment, promoted by selective dissolution of the α-Al phase stimulated by galvanic coupling with noble silicon precipitates at the border of the melt pool. Such penetrating morphology was not observed after heat treatments at high temperature. 相似文献
10.
In a previous study a mathematical model relating surface and bulk behaviors of metals in aqueous solution was developed. The model was established based on principles of holographic interferometry for measuring microsurface dissolution, i.e., mass loss, and on those of electrochemistry for measuring the bulk electronic current, i.e., corrosion current. In the present work, an interferometric sensor was built based on the above model, and the corrosion current density of coated copper and brass in seawater were obtained using this sensor. The interferometric sensor was also utilized for the first time to measure the initial stage of the anodization process (oxidation) of aluminium samples in aqueous solution. This was carried out chemically in different acid concentrations (3.125–25% H2SO4) at room temperature. The sensor was further used for observation of catalytic activities, i.e., pitting corrosion, which occurred subsequent to the anodization of the aluminium samples in aqueous solutions, after an oxide film had been formed. 相似文献