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The recovery of anthocyanins from winery wastewater constitutes an attractive option for both environmental and commercial valorization, as food colorants and nutraceutical ingredients. In this study, the electric field induced ion drift method is proposed as a promising technique for the purification of wastewater solutions as well as for the accumulation of anthocyanins. The cation of the anthocyanidin malvidin (C17H15O7+) was selected as the most representative of winery waste, in order to develop a theoretical model. The main principle of the model is based on the displacement of charged anthocyanin ions, under the influence of an electric field vertical to the flow of the solution, and their accumulation on the side walls of a conductor. Apparatus inducing an electric field drift is described, and critical parameters (i.e., final spatial distribution of concentration, electric field intensity, surface charge density, and potential) were calculated. The proposed model succeeded in reducing anthocyanin concentration by more than 90%, for duct widths smaller than 1 mm in the bulk of the solution, for applied potentials φ(0) in the range of 0.2–0.4 V and target concentrations equal to 1.2 × 10−3 mol/m3. [ABSTRACT FROM AUTHOR]

Desalination and water purification through the ion drift of salted water flow due to an electric field in a duct is perhaps a feasible membrane-free technology. Here, the unsteady modulation of ion drift is treated by employing the Poison–Nernst–Plank (PNP) equations in the linear regime. Based on the solution of the PNP equations, the closed-form relationships of the charge density, the ion concentration, the electric field distribution and its potential are obtained as a function of position and time. It is found that the duration of the ion drift is of the order of one second or less. Moreover, the credibility of various electrical circuit models is examined and successfully compared with our solution. Then, the closed form of the surface charge density and the potential that are calculated without the linear approximation showed that the compact layer is crucial for the ion confinement near the duct walls. To test this, nonlinear solutions of the PNP equations are obtained, and the limits of accuracy of the linear theory is discussed. Our results indicate that the linear approximation gives accurate results only at the fluid's bulk but not inside the double layer. Finally, the important issue of electric field diminishing at the fluid's bulk is discussed, and a potential method to overcome this is proposed. [ABSTRACT FROM AUTHOR]