Electrochemical disinfection of groundwater for civil use - An example of an effective endogenous advanced oxidation process.

Lab-scale experiments using real groundwater were carried out using the CabECO reactor system in order to evaluate its suitability for producing safe water, acceptable for civil purposes. Trials were carried out in discontinuous and in continuous mode, analyzing the influence of electrical and hydraulic process parameters on the quality of treated water. The use of highly boron-doped diamond electrodes in the reactor allowed the electrosynthesis of considerable amounts of ozone.

The use of ECAS in plant protection: a green and efficient antimicrobial approach that primes selected defense genes.

The use of highly polluting chemicals for plant and crop protection is one of the components of the negative environmental impact of agricultural activities. In the present paper, an environmentally friendly alternative to pesticide application has been studied, based on the so-called electrochemically activated solutions (ECAS). Experiments have been carried out, by applying ECAS having different contents of active ingredients, on tobacco plants at a laboratory scale and on apple trees at fruit garden scale.

Scale-up of electrochemical oxidation system for treatment of produced water generated by Brazilian petrochemical industry.

Scale-up of anodic oxidation system is critical to the practical application of electrochemical treatment in bio-refractory organic wastewater treatment. In this study, the scale-up of electrochemical flow system was investigated by treating petrochemical wastewater using platinized titanium (Ti/Pt) and boron-doped diamond (BDD) anodes. It was demonstrated that flow cell was successfully scaled-up because when it was compared with batch mode (Rocha et al.

Heterogeneous electron-transfer rate constants for fe(h(2)o)(6)(3+/2+) at metal oxide electrodes.

The title redox couple, in noncoordinating perchlorate medium, has been used to probe the electrochemical behavior of different IrO2-based electrodes; pure oxide electrodes, as well as IrO2-SnO2 mixtures, have been investigated. The obtained results show that the electrode material strongly affects the electrochemical response. A tentative explanation, based on the different point of zero charge of the considered oxides, is presented.

Removal of the pesticide methamidophos from aqueous solutions by electrooxidation using Pb/PbO2, Ti/SnO2, and Si/BDD electrodes.

The anodic oxidation of methamidophos (MMD), a highly toxic pesticide used worldwide, was studied in a sodium sulfate aqueous solution on Pb/PbO2, Ti/SnO2, and Si/BDD (boron doped diamond) electrodes at 30 degrees C. Under galvanostatic conditions, it was observed thatthe performance of the electrode material is influenced by pH and current density as shown by HPLC and ATR-FTIR analysis of MMD and its oxidation products along the electrolysis. It was found that MMD degradation using Pb/PbO2 in acid media (pH 2.

Surface chemistry study of RuO2/IrO2/TiO2 mixed-oxide electrodes.

DSA metal oxide electrodes such as the RuO(2)/IrO(2)/TiO(2) mixed system are widely studied for their excellent electrocatalytic activity. In order to understand their catalytic properties, the comprehension of the surface chemistry involved during electrochemical treatments is crucial. With this aim, RuO(2)/IrO(2)/TiO(2) mixed-oxide electrodes having various noble metal contents were studied by means of secondary ion mass spectrometry (SIMS).

The 5-V window of polarizability of fluorinated diamond electrodes in aqueous solutions.

Heavily doped diamond films are quite actively studied for their promising applications in industrial as well as in fundamental electrochemistry (both for physicochemical studies and in the field of electroanalysis), because of their very high stability toward chemical and electrochemical oxidative attacks. Fluorinated diamond electrodes exhibit an exceptionally lower electrocatalytic activity toward reactions involving adsorbed intermediates, as a result of the F-termination of the surface dangling bonds. This feature allows the investigation of the widest range of potentials for an electrode material in aqueous solution, being limited only by the formation of free hydrogen [E degrees (H*/H2) = -2.