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Rafael Sotana

Publications and source records attributed to Rafael Sotana.

2 recordsLinked to original sources

Flower-like WO3-modified Vulcan carbon GDEs for photoelectro-Fenton process: Efficient ciprofloxacin degradation and mechanistic insights

Electrochemical H2O2 synthesis was investigated using a 3 percent WO3 C gas diffusion electrode GDE. The catalyst outperformed bare Vulcan carbon, generating H2O2 concentrations of 423, 586, and 916 mg L at 50, 75, and 100 mA cm2, respectively, maintaining around 70 percent current efficiency. This performance and lower energy consumption are attributed to the WO3 carbon synergistic effect. In electro Fenton EF applications, the WO3 C GDE achieved rapid initial ciprofloxacin CIP degradation of around 70 percent in 30 min, though limited later by slow Fe2 regeneration. Incorporating UV light photoelectro Fenton overcame this constraint, yielding complete CIP removal within 90 min, while a boron doped diamond BDD anode enhanced total organic carbon TOC mineralization to 66 percent. The proposed degradation mechanism proceeds via hydroxyl radical attack on the piperazine ring with or without defluorination and quinolone ring oxidation, with theoretical analysis confirming reduced environmental toxicity of the transformation products. Overall, WO3 C GDEs represent a highly efficient strategy for H2O2 generation and wastewater remediation.

cond-mat.mtrl-sci↗

Electron Paramagnetic Resonance Study of Radical Species on NaNbO3@CeO2-Modified Carbon Vulcan XC72 Gas Diffusion Electrode for Electrochemical Degradation of Paracetamol via Electro-Fenton

While electrochemical oxidation is a promising technology for water treatment, a fundamental understanding of the specific radical mechanisms involved in pharmaceutical degradation has remained limited. This study addresses this gap by employing Electron Paramagnetic Resonance (EPR) spectroscopy to directly quantify the radical species generated during the degradation of paracetamol using a novel gas diffusion electrode (GDE) modified with NaNbO3 nanocubes and CeO2 nanorods. This approach provides a critical advancement beyond prior literature by moving from indirect inference to direct, quantitative analysis of reactive species. Results demonstrated that a boron-doped diamond (BDD) anode (65% OH radical, 35% aryl radicals) drastically outperformed a Platinum (Pt) anode (74% OH radical, 26% aryl radicals), achieving complete degradation in 15 minutes versus 45 minutes and 81.6% versus 67.8% mineralization. Consequently, this work provides a foundational mechanistic framework that fundamentally advances the field, offering not just a more effective material system (BDD/NaNbO3@CeO2-GDE) but also a validated methodology for rationally designing and optimizing electrochemical water treatment processes based on quantifiable radical pathways.

physics.chem-ph↗