Espinoza Montero, Patricio Javier2023-11-042023-11-0420181870-249Xhttps://doi.org/10.29356/jmcs.v62i2.367http://www.scielo.org.mx/pdf/jmcs/v62n2/1870-249X-jmcs-62-02-00295.pdfhttps://repositorio.puce.edu.ec/handle/123456789/4534Nowadays, the increasing pollution of natural water effluents with herbicides, such as atrazine (ATZ, 2-chloro-4-ethylamino-6-isopropylamino-s-triazine), is an emerging problem that has not received the sufficient attention. This work presents a study on ATZ degradation under an electrochemical advanced oxidation process (EAOP), such as anodic oxidation (AO). The degradation of 175 mL of 10 and 40 mg L-1 ATZ solutions was studied using Pt or BDD as anode. The assays were made with a stirred tank cell, using a supporting electrolyte of 0.050 mM of Na2SO4 at pH 3.0 by applying 0.18, 0.27 and 0.37 A cm-2. The degradation rate increased by increasing current density, regardless of the anode employed. Greater amounts of ATZ were removed at higher organic load. The pesticide decay always obeyed a pseudo-first-order kinetics. A high degradation efficiency of 97%-99% was obtained by the more powerful AO-BDD process at 0.37 A cm-2. High performance liquid chromatography (HPLC) was used to follow the evolution of major oxidation products by AO-BDD, such as desethyl atrazine, desethyl desisopropyl atrazine and cyanuric acid.OpenAccessAgua - TratamientoOxidaciónAtrazina