Showing 4 results for Potentiodynamic Polarization
Alah Karam S.r., Alah Karam S.r.,
Volume 1, Issue 1 (3-2004)
Abstract
In this paper redox reaction processes and phase, formation on ternary Pb-2Sn-0.08Ca alloy utilized as insoluble lead anodes in copper electro winning cells, were investigated in 2M H__2SO__4 electrolytes, using cyclic voltammetry technique (CVA). A potential range between - 1.3V to 2.6V was chosen at various scan rates in order to study the anodic behavior and phase composition of the oxide layers on Pb-2Sn-0.08Ca alloy. Potential measurements were carried out with respect to a standard calomel electrode (SCE). The surface examination and phase composition of the lead alloy were determined by electron microscopy analysis (SEM) and x-ray diffraction technique, after- exposure to the cyclic voltammetry tests. The results indicated that the protective oxide layer (Pb0__2) formed at a much slower rate when exposed to 2M H__2SO__4 solutions, whilst its degradation due to a reduction in the applied potential occurred at a much faster rate. Hence, Pb0__2 did not remain stable, when the externally applied potential dropped below 1.SV and as a result, pitting initiated sporadically on the surface of the electrode.
Moayed M.h.,
Volume 2, Issue 3 (9-2005)
Abstract
In this research pitting Corrosion of a sensitized 316 stainless steel was investigated employing potentiodynamic, potentiostatic techniques. Sensitization process was carried out on as-received alloy by submitting the specimen in electric furnace set at 650°Cfor five hours and then the specimen was quenched 25°C water. Potentiodynamic polarization of as received and sensitized specimens in 1M H2SO4 solution at room temperature and 70°C clearly revealed that the sensitization process has caused a magnificent change on electrochemical behavior of the specimen by changing critical current density for passivation, passivation potential and passive current density. Optical microscopy examination of the specimen surface after oxalic acid electrochemical etching also showed the deterioration of grain boundary of sensitized specimen due to chromium carbide precipitation in compared to as-received one. Several anodic potentiodynamic polarization on rode shaped working electrodes prepared from as-received and sensitized specimen in 3.5% NaCl test solution proved an average ~220 mV drop in pitting potential due to sensitization. Anodic potentiostatic polarization at 400 and 200 mV above corrosion potential also demonstrate the deterioration of pitting resistance of alloy as a result of sensitization. Scanning electron microscopy examination of anodically polarized of sensitized specimen at 700mVprior and after oxalic acid etching revealed large stable pits with lacy cover and also openpits with deep crevice for etched specimens.
Sh. Shahriari, M. Ehteshamzadeh,
Volume 10, Issue 1 (3-2013)
Abstract
Abstract: Plasma electrolytic oxidation (PEO) technique was used to prepare ceramic coatings on the casted aluminum alloys containing ~5 and ~9.5 wt.% Mg. The applied voltage was controlled at 450V and 550V for evaluating the effect of this main parameter, as well as, magnesium content of the substrate on the microstructure and electrochemical corrosion behavior after PEO treating. The results of X-ray diffraction confirmed formation of galumina and MgSiO3. It was found that higher applied voltage caused fewer and minor discharge channels which led to higher corrosion resistance. Also, increasing of magnesium content of the substrate caused decreasing of polarization resistance, which could be associated to the formation of MgSiO3.
A. Fattah-Alhosseini, H. Farahani,
Volume 10, Issue 4 (12-2013)
Abstract
The effects of H2SO4 concentration on the electrochemical behaviour of passive films formed on AISI 304 stainless steel were investigated using by potentiodynamic polarization, Mott–Schottky analysis and electrochemical impedance spectroscopy (EIS). Potentiodynamic polarization indicated that the corrosion potentials were found to shift towards negative direction with an increase in solution concentration. Also, the corrosion current densities increase with an increase in solution concentration. Mott–Schottky analysis revealed that the passive films behave as n-type and p-type semiconductors at potentials below and above the flat band potential, respectively. Also, Mott– Schottky analysis indicated that the donor and acceptor densities are in the range 1021 cm-3 and increased with solution concentration. EIS data showed that the equivalent circuit Rs(Qdl[Rct(RrQr)]) by two time constants is applicable.
