Abstract
In this work, a gas diffusion electrode (GDE) made of Printex L6 carbon modified with 2.0% w/w of benzophenone-3,3′,4,4′-tetracarboxylic dianhydride (PL6C/BTDA 2%) was employed as cathode in a new 3D printed electrochemical cell with tangential flow. With this configuration, the performance of the technology was evaluated for hydrogen peroxide (H2O2) electrogeneration and remediation of aqueous wastes contaminated with diethyl phthalate (DEP) using different H2O2-based advanced oxidation processes (AOPs). The electrogeneration study was carried out varying the current density applied to the system, and it was found that 50 mA cm-2 was the best performing value, resulting in remarkable Faradaic efficiencies of nearly 100%. This led to the production of higher amounts of H2O2 (442.5 mg L-1) in 90 minutes at an acceptable energy consumption (8.5 kWh kg-1) compared to values reported in the literature. Based on these findings, H2O2-based AOPs were employed to investigate the removal of DEP in cathodic compartment, including mediated electrochemical degradation with electrogenerated H2O2 (e-H2O2) and the integration of this technology with ultraviolet-C (UVC) photolysis (e-H2O2/UVC). The integrated e-H2O2/UVC obtained the best performance compared to single photolysis and e-H2O2, leading to the total elimination of DEP (90 μmol L-1) within only 30 min of treatment, reaching the highest kinetic rate constant (0.3 min-1). Fifteen by-products, generated through oxidation processes studied, were successfully identified by LC-MS/MS, enabling the proposal of the degradation mechanism of DEP.
Published Version
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