The corrosion behavior of tin bronze alloy equivalent to a Punic one was investigated in aqueous 0.5 M chloride electrolyte using potentiodynamic measurements. The electrochemical results showed selective dissolution of the major alloy component reflecting a decuprification process. FTIR characterization of the patina anodic layers showed the presence of various dehydrated and hydrated tin compounds with a few copper species suggesting the patina type I formation on the Cu10Sn bronze alloy. A kinetic model for the Cu10Sn bronze alloy dissolution in the chloride solution was developed. The reaction order with respect to chloride content was determined for the Cl− halide concentration domains. The low order value (about 0.22) was attributed to the Cl− adsorption intermediate step. The high reaction order value (about 2) reflected two determining steps of cuprous chloride complex formation. Two behaviors for the material were evidenced when varying the temperature. The values of the activation energy Ea, activation enthalpy ΔH* and activation entropy ΔS* were calculated and discussed.

Plackett–Burman experimental design was carried out in order to optimize the experimental conditions of polyaniline (PANI) electrodeposition for Cu10Sn bronze alloy corrosion protection in neutral aerated aqueous 0.5 M chloride medium. Seven factors including scan rate, aniline concentration, hydroxyl ions concentration, cycle number, nature of solvent, starting potential, and final potential for the cyclic voltammetry study were considered. The experimental responses were Ecorr, βa, βc, B, Jcorr, Rp, the percentage of protection efficiency and the coatings porosities. A linear mathematical model was applied to estimate the coefficients related to the different experimental responses. The significance of the different factors was evaluated through Pareto analysis. The optimum conditions for PANI electrodeposition were estimated and discussed. PANI coatings were concluded to offer protection efficiency higher than 90% for Cu10Sn bronze alloy. Copyright © 2016 John Wiley & Sons, Ltd.

The aim of the present investigation was to model the experimental conditions of tin bronze patination using full factorial experimental design. In this sense, a full factorial design approach was developed to model the corrosion behavior of patinated tin bronze alloy in sulfate electrolyte. Three experimental factors (the immersion time in the chloride electrolyte, the potential limit for the anodic sweep Elim, and the potential scan rate) were chosen to identify the significant factor on the patina growth process at the bronze substrate. The experimental responses were the kinetic parameters extracted from the electro-chemical spectra (EIS) for eight different experiments. An equivalent electrical circuit containing an electrolyte resistance (Re), a double layer capacitance (CPE dl ), a charge transfer resistance (R t ) and Gerischer element (G), was developed to model the patinated bronze corrosion process. The electro-chemical spectra (EIS) show that the corrosion process of the patinated bronze alloy occurred from a chemical reaction is followed by an electrochemical one. Analysis of the experimental responses showed that while the scan rate is the most influent factor for the corrosion potential (E corr ), the electrolyte resistance (Re), and the double layer capacitance CPE dl variation, the potential limit is the significant factor for charge transfer resistance Rt, reciprocal of the admittance parameter Y 0 and the effective transfer rate of the chemical reaction k variation.