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The electrochemical oxidation of aqueous wastes containing 4-nitrophenol (4-NP) using a borondoped diamond thin-film electrode has been studied. Within the parameter ranges used (150-4000 mg of 4-NP dm -3 , pH 2-12, 30-60 mA cm -2 , 25-60 °C), the complete treatment of the organic waste was achieved. The maximum current efficiencies were obtained under kinetic control. On the basis of the results of voltammetric and galvanostatic electrolysis studies, a simple mechanistic model was proposed. The first stage in the treatment of 4-NP-containing aqueous wastes is the release of the nitro group from the aromatic ring. As a consequence, phenol or quinones are formed. These organic compounds are oxidized first to carboxylic acids (maleic and oxalic) and later to carbon dioxide. On the cathode, the reduction of the 4-NP to 4-aminophenol takes place. In alkaline media, this compound can be polymerized and transformed into a dark brown solid.

The electrodissolution of aluminum electrodes in aqueous solutions containing sulfate or chloride ions is studied in this work. The results obtained are important in order to obtain a better understanding of the electrocoagulation process, as the electrodissolution of the anode surface is its first step. It has been determined that both chemical and electrochemical dissolution play an important role in the aluminum generation. The chemical dissolution of aluminum is strongly influenced by the pH. Alkaline pHs increase the dissolution rate by orders of magnitude. Within the experimental conditions used, the supporting media does not seem to influence greatly the chemical dissolution process. The electrochemical dissolution process depends mainly on the specific electrical charge passed. Salinity does not significantly affect the electrodissolution rate. Good fittings between experimental and modeled data are obtained by modeling the system with a simple model based on two assumptions:  a highly segregated flow pattern and the calculation of aluminium species and pH from a pseudoequilibrium approach.

Dyes are common pollutants in a large variety of industrial wastewaters, and the treatment of these wastes by coagulation has been extensively studied in the literature. This work is focused on the comparison of the efficiencies of the chemical and the electrochemical coagulation processes with hydrolyzing aluminum salts, and it tries to determine the similarities or differences that exist between the two coagulation processes. To do this, Eriochrome Black T solutions were used as a model of dye-polluted wastewater, and experiments of both coagulation technologies were planned to meet the same operation conditions. The pH, the aluminum concentration, the type of electrolyte, and the mode of dosing of aluminum were found to influence the process. Moreover, the speciation of aluminum was found to be the key parameter to explain the results, in terms of the mechanisms previously proposed in the literature for dissolved organic matter coagulation.

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