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Uniform conducting polymer films of poly(N-(1-Naphthyl) ethylene-diamine dihydrochloride), PNED, were prepared conveniently and reproducibly by the anodic oxidation of the monomer, N-(1-Naphthyl) ethylene-diamine dihydrochloride, NED, in an acidic aqueous solution using the conventional potentiodynamic technique. The different parameters influencing the preparation conditions like monomer concentration, solvent constitution, scan range, scan rate, scan repetition, rotation speed of the working electrode and the type of the substrate were investigated and the optimum preparation conditions are specified. The stability of the prepared films was tested in both aqueous and non-aqueous media. The characteristics of the polymer films and their electrochemical activity towards catalyzing some technologically promising redox reactions were also examined. The films were found to be very stable in aqueous solutions and in some organic solvents like acetone, acetonitrile, and chloroform and dimethyl sulfoxide. The film stability was found to depend on the solution pH. The polymer films were capable of catalyzing the redox processes of several natural products and amino acids e.g. vitamin C and glycine. The polymer film possesses electrochromic properties and the color of the film changes from purple to violet to dark blue and then to brown according to the preparation and/or polarization conditions. The electrochromic properties are related to polaron formation, which subsequently oxidizes to diimine species followed by the oxidation of the aromatic ring. The mechanism of the polymerization process was investigated and discussed. The process involves deprotonation reactions and a head-to-tail coupling of the oxidized monomer with cation radicals.

The corrosion and passivation behaviors of alloys with different Cu–Ni ratios were investigated in acidic sulfate solutions. The corrosion rate was calculated and the corrosion inhibition process was investigated using different amino acids as corrosion inhibitors. For these investigations conventional electrochemical techniques and electrochemical impedance spectroscopy (EIS) were used. Fitting of the experimental impedance data to theoretical values enables understanding of the corrosion inhibition mechanism and the suggestion of a suitable electrical model to explain the behavior of the alloys under different conditions. The investigation of the electrochemical behavior of alloys before and after the corrosion inhibition processes has shown that some amino acids like lysine have promising corrosion inhibition efficiency at very low concentrations. A model for the electrode/electrolyte interface during the corrosion inhibition processes was suggested and the validity of the model for the explanation of the corrosion inhibition phenomena was discussed.

The electrochemical behaviour of copper–nickel alloys with different Ni content (5–65%) in sulphate solutions of pH 12 was investigated. The effects of temperature, immersion time, and concentration of sulphate ions were also studied. Different electrochemical methods such as open-circuit potential measurements, polarization techniques and electrochemical impedance spectroscopy (EIS) were used. Potentiodynamic measurements reveal that the increase in nickel content increases the corrosion rate of the alloy in sulphate solution linearly. Nevertheless, an increase in the nickel content along with increase in immersion time improves the stability of the Cu–Ni alloys due to the formation of a stable passive film. An equivalent circuit model for the electrode/electrolyte interface under different conditions was proposed. The experimental impedance data were fitted to theoretical data according to the proposed model. The relevance of the model to the corrosion/passivation phenomena occurring at the electrode/solution interface was discussed.

The electrochemical behaviour of brasses with various Zn content (5.5–38) and brass (Cu–38Zn) with different Pb content (1.3–3.3) in borate solution, pH 9.0, was investigated. The effects of applied potential and the presence of aggressive Cl− ions were also studied. Different electrochemical methods such as open-circuit potential measurements, polarization techniques and electrochemical impedence spectroscopy (EIS) were used. Increase in zinc content decreases the corrosion rate of brass in borate solution exponentially. Long immersion of leaded brasses and alloys with different Zn content improves their stability due to the formation of a passive film. The passive film formation under open-circuit and potentiostatic conditions proceeds via dissolution–precipitation mechanism. The addition of a low concentration of Cl− ion (0.01 M) to the borate solution increases the corrosion rate of Cu–38Zn due to dezincification. Increase in Cl− ion concentration (0.01–0.2 M) decreases the corrosion rate of the brass exponentially due to formation of insoluble CuCl. For Cl− ion concentrations >0.2 M the corrosion rate of the brass increases again due to the formation of the soluble CuCl2 − complex.