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Integration of sub-stoichiometric titanium oxide reactive electrochemical membrane as anode in the electro-Fenton process

Trellu, Clément and Rivallin, Matthieu and Cerneaux, Sophie and Coetsier, Clémence and Causserand, Christel and Oturan, Mehmet A. and Cretin, Marc Integration of sub-stoichiometric titanium oxide reactive electrochemical membrane as anode in the electro-Fenton process. (2020) Chemical Engineering Journal, 400. 125936. ISSN 1385-8947

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Official URL: https://doi.org/10.1016/j.cej.2020.125936


Sub-stoichiometric titanium oxide (TiOx) reactive electrochemical membrane (REM) were integrated for the first time as anode in the electro-Fenton (EF) process. Hydroxyl radicals (•OH) were produced both in the retentate from Fenton's reaction and at the REM from anodic oxidation (AO). Optimal mass transport conditions were implemented because of convection-enhanced mass transport of (i) organic pollutants towards the REM surface during filtration and (ii) dissolved 02 towards cathode active sites owing to the use of a 3D carbon felt cathode in flow-through configuration for H202 generation. The efficiency of the REM/EF process was much higher than EF or REM used as standalone processes. For instance, taking paracetamol as target pollutant, (67 ± 2)% removal of 55 mg L - i of initial TOC was achieved with a high mineralization current efficiency (MCE) of ( 43 ± 1)%. By comparison, standalone REM and EF processes achieved only 47% (MCE = 30%) and 31 % (MCE = 20%) of TOC removal, respectively. By monitoring TOC removal both in retentate and permeate, the effect of homogeneous oxidation in the bulk retentate and heterogeneous oxidation at the REM could be observed separately. It was thus highlighted that the efficiency of AO might be affected by the presence of • OH and Fe2 + in the bulk. It was also emphasized a synergistic effect related to the formation of carboxylic acids in the bulk retentate that are more easily mineralized at the REM where both • OH-mediated oxidation and direct electron transfer occur.

Item Type:Article
HAL Id:hal-03117332
Audience (journal):International peer-reviewed journal
Uncontrolled Keywords:
Institution:French research institutions > Centre National de la Recherche Scientifique - CNRS (FRANCE)
Other partners > Ecole Nationale Supérieure de Chimie de Montpellier - ENSCM (FRANCE)
Université de Toulouse > Institut National Polytechnique de Toulouse - Toulouse INP (FRANCE)
Other partners > Université Gustave Eiffel (FRANCE)
Université de Toulouse > Université Toulouse III - Paul Sabatier - UT3 (FRANCE)
Other partners > Université Paris-Est Marne-La-Vallée - UPEM (FRANCE)
Other partners > Université de Montpellier (FRANCE)
Laboratory name:
Deposited On:21 Jan 2021 09:04

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