Al-Si hypoeutectic alloys produced by casting are mostly used in the automotive industry, especially for engine blocks. They have the advantage of low weight associated with low coefficient of thermal expansion and excellent mechanical properties. The corrosion resistance of these alloys in coastal area, particularly in seawater environment is not well known. In this investigation, electrochemical impedance spectroscopy (EIS) and potentiodynamic polarisation have been used to evaluate the corrosion resistance of Cu free and 0.5wt% Cu content Al-6Si-0.5Mg alloy in simulated seawater environment. The 0.5wt% Cu addition to the Al-6Si-0.5Mg alloy showed that Cu decreased susceptibility to electrochemical corrosion compared to the Cu free Al-6Si-0.5Mg alloy. The magnitude of open circuit potential (OCP), corrosion potential (Ecorr) and pitting corrosion potential (Epit) of Al-6Si-0.5Mg alloy in simulated seawater were shifted to the more noble direction due to 0.5wt% Cu addition and thermal modification.
The purpose of this paper is to understand the effect of 2Cu+2Ni addition on electrochemical corrosion behavior of thermal treated Al-6Si-0.5Mg alloy in 0.1M NaCl solution. The corrosion of the thermal treated samples was characterized by electrochemical potentiodynamic polarization technique consisting of linear polarization method using the fit Tafel plot and electrochemical impedance spectroscopy (EIS) techniques. Generally, from the linear polarization, the corrosion rate decreases at thermal treated Al-6Si-0.5Mg-2Cu-2Ni alloy (Alloy-2). The corrosion behavior of the Alloy-2 in the 0.1M NaCl solution showed better resistance than the Alloy-1. The EIS test results also showed that the changing of charge transfer resistance (Rct) is significant with the combined addition of 2Cu+2Ni to Al-6Si-0.5Mg alloy. The magnitude of the noble shift in the open circuit potential (OCP), corrosion potential (Ecorr) and pitting corrosion potential (Epit) increased with the addition of 2Cu+2Ni to Al-6Si-0.5Mg alloy.
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In the present investigation we have galvanostatically synthesized Co-Ni nanocrystalline alloys on copper substrate. The effect of current density (c.d.) on composition, surface morphology and phase structure were studied for explaining the magnetic and corrosion resistance of the alloy. The bath found to exhibit the preferential deposition of less noble Co than Ni, and at no conditions of c.d., the deposition has changed from anomalous to normal type. Surface morphology and structural characteristics of the deposits were examined using scanning electron microscopy (SEM) and X-ray diffraction (XRD) analysis. As composition of the alloy varied, consequent to the c.d. a change of hexagonal close packing structure (hcp) to face centered cubic structure (fcc) was observed. Finally, the conditions responsible for peak magnetic property and corrosion resistance were optimized. Factors responsible for improved functional properties were explained in terms of surface morphology and crystalline grain size of the coatings.
The inhibiting effect of molybdate, chromate, and tungstate salts on the corrosion of steel used in sanitation plants was investigated by potentiodynamic polarization, electrochemical impedance spectroscopy (EIS), and electrochemical frequency modulation (EFM) techniques. The sulfide polluted salt water was simulated by a 3.5 % NaCl and 16 ppm Na2S solution. The results revealed that these inorganic anions are very good inhibitors. Potentiodynamic polarization curves indicated an anodic-type inhibition. The increased concentration of inorganic compounds increases the inhibition; at 250 ppm concentration the inhibition efficiency reached to 95 %, 91.6 %, and 87.5 % for MoO42-, CrO42-, and WO42-, respectively. The adsorption of the inhibitors on the metal surface basically obeys the Langmuir adsorption isotherm equation. Results of EIS measurements suggested that the dissolution of the steel occurs under activation control, and a passive film is probably formed on the metal surface. The electrochemical kinetic parameters calculated from EFM spectra confirm the polarization data.