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               <dc:title>Paired electrochemical removal of nitrate and terbuthylazine pesticide from groundwater using mesh electrodes</dc:title>
               <dc:creator>Oriol López, Roger</dc:creator>
               <dc:creator>Brillas Coso, Enrique</dc:creator>
               <dc:creator>Cabot, Pere-Lluis</dc:creator>
               <dc:creator>Cortina Pallás, José Luis</dc:creator>
               <dc:creator>Sirés Sadornil, Ignasi</dc:creator>
               <dc:subject>Àrees temàtiques de la UPC::Enginyeria química</dc:subject>
               <dc:subject>Electrochemistry</dc:subject>
               <dc:subject>Boron-doped diamond anode</dc:subject>
               <dc:subject>Electrochemical oxidation</dc:subject>
               <dc:subject>Electrodenitrification</dc:subject>
               <dc:subject>Groundwater</dc:subject>
               <dc:subject>Iron cathode</dc:subject>
               <dc:subject>Electroquímica</dc:subject>
               <dc:description>Groundwater is one of the main freshwater resources on Earth, but its contamination with NO3- and pesticides jeopardizes its viability as a source of drinking water. In this work, a detailed study of single electro-oxidation (EO) and electrodenitrification and paired EO/electrodenitrification processes has been undertaken with simulated and actual groundwater matrices containing 100 mg dm-3 NO3- and/or 5 mg dm-3 terbuthylazine pesticide. Galvanostatic electrolyses were made with 500 cm3 of solutions at pH 4.0-10.5 and 250-1000 mA in tank reactors with a RuO2 or boron-doped diamond (BDD) anode and one or two Fe cathodes, all of them in the form of meshes. Most of NO3- removals agreed with a pseudo-first-order kinetics. In Cl--free media, NH4+ predominated as electroreduction product. In chloride media, a greater amount of N-volatiles was determined alongside a slower electrodenitrification, especially with RuO2 due to the partial re-oxidation of electroreduction products like NH4+ by active chlorine. The pesticide decays were also fitted to a pseudo-first order kinetics, and its presence led to a smaller release of N-volatiles. Overall, BDD always favored the pesticide degradation thanks to the action of BDD(&#xd;
&#xd;
OH), whereas RuO2 was preferred for electrodenitrification under some conditions. The EO/electrodenitrification of groundwater was successful once the matrix was softened to minimize its hardness. The NO3- concentration was reduced below the limit established by the WHO. Overall, the BDD/Fe cell was more suitable than the RuO2/Fe cell because it accelerated the pesticide removal with a simultaneous high degree of NO3- electroreduction. However, it produced toxic chlorate and perchlorate. A final post-treatment with an anion exchange resin ensured a significant removal of both ions, thus increasing the viability of the electrochemical approach to treat this type of water. Chromatographic analyses revealed the formation of ten heteroaromatic products like desethyl-terbuthylazine and cyanuric acid, alongside oxalic and oxamic as final short-chain carboxylic acids.</dc:description>
               <dc:description>Peer Reviewed</dc:description>
               <dc:description>Postprint (author's final draft)</dc:description>
               <dc:date>2021-07-01</dc:date>
               <dc:type>Article</dc:type>
               <dc:relation>https://www.sciencedirect.com/science/article/abs/pii/S0013468621006447</dc:relation>
               <dc:rights>http://creativecommons.org/licenses/by-nc-nd/3.0/es/</dc:rights>
               <dc:rights>Open Access</dc:rights>
               <dc:rights>Attribution-NonCommercial-NoDerivs 3.0 Spain</dc:rights>
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