Polypyrrole (PPy) films of different thickness were characterized by electrochemical impedance spectroscopy (EIS) measurements in acetonitrile and aqueous solutions, containing 0.1 M NaClO4 or sodium dodecylsulfate as the dopant. The PPy films were electrochemically deposited on Pt, and their electrochemical properties studied by cyclic voltammetry. Impedance spectra were obtained at potentials ranging from 0 to 0.8 V/SCE. The EIS data were fitted using two different equivalent electrical circuits (depending on the nature of the dopant). They involve a diffusive capacitance, which increased with the passing charge during electrosynthesis (i.e. film thickness) for ClO4-doped PPy, but was practically unaffected by the film thickness in the case of SDSdoped PPy. Also, a double-layer capacitance was found only in the circuit of ClO4-doped PPy. It increased with the film thickness, and showed a minimum near the open-circuit potential. Finally the charge-transfer resistance (Rct) obtained with SDS is nearly 200-fold higher than that obtained with ClO4in the same solvent (H2O). With the same dopant (ClO4-), Rct is about five times higher in acetonitrile relative to water. All these EIS results of the different types of PPy suggest a relation with the wettability of the polymer.

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ABSTRACT. The corrosion behavior of three constructional steels used in Senegal, S235, S275 and S355, was studied in simulated atmospheric conditions in an exposure chamber above distilled water and above 3% NaCl solution representing marine atmosphere by comparing the ratio of rusted to unrusted area. Electrochemical test methods (potentiodynamic tests and electrochemical impedance spectroscopy) were employed to study the steels fully immersed in acidic, near neutral and basic conditions in 0.5 M HCl, NaCl, and NaOH solutions, respectively. Results indicate that S355 and S235 steels have comparable corrosion resistance, which are much lower than that of S275.

A comparative study of two electro-physical properties (porosity and electrical conductivity) of binary nickel cobalt oxides electrodes with spinels mixed oxides Ni x Co 3-x O 4 as active matter, was carried out. Four different routes were used to prepare spinel-type Ni x Co 3-x O 4 (0 ≤ x ≤ 2.5) compounds in order to link these properties with the preparation method. The substitution of Ni for Co increases the conductivity and the porosity of the electrode till a certain ratio of nickel. X-ray diffraction patterns showed that the oxides crystallize in a cubic spinel phase. Electrical conductivity as well as porosity depends on the preparation route.

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