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Vanessa S. Antonin

Publications and source records attributed to Vanessa S. Antonin.

4 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↗

Improvement of H$_2$O$_2$ electrogeneration using a Vulcan XC72 carbon-based electrocatalyst modified with Ce-doped Nb$_2$O$_5$

The use of the oxygen reduction reaction (ORR) for in-situ production of H$_2$O$_2$ is an attractive alternative to replace the methods based on anthraquinone oxidation. This study investigates the modification of Vulcan XC72 carbon with Ce-doped Nb$_2$O$_5$ in different molar proportions and its application as electrocatalysts in the ORR. One performed the characterization of the electrocatalysts using X-ray diffraction, Raman spectroscopy, scanning electron microscopy, transmission electron microscopy, contact angle measurements, and X-ray photoelectron spectroscopy. Subsequently, the electrocatalysts were analyzed for the ORR and the Nb$_2$O$_5$ doped with 0.5% Ce showing the highest electrocatalytic response. This electrocatalyst was also employed as a gas diffusion electrode and exhibited more significant H$_2$O$_2$ production at all potentials than the Vulcan XC72 carbon modified solely with Nb$_2$O$_5$. At the applied potentials of -1.3 V and -1.9 V, it produced 105% and 86% more H$_2$O$_2$, respectively, than the Vulcan XC72 carbon modified only with Nb$_2$O$_5$. These results can be attributed to the doping of Nb$_2$O$_5$ with 0.5% Ce, which induces local distortions in the crystal lattice of Nb$_2$O$_5$ due to the difference in ionic radius between Nb$^{5+}$ and Ce$^{3+}$, which combined with increased hydrophilicity and wetting properties, may have facilitated electron transfer and O$_2$ transport, favoring the ORR.

cond-mat.mtrl-sci↗

Hydrogen peroxide electrogeneration from O2 electroreduction: a review focusing on carbon electrocatalysts and environmental applications

Hydrogen peroxide (H2O2) stands as one of the foremost utilized oxidizing agents in modern times. The established method for its production involves the intricate and costly anthraquinone process. However, a promising alternative pathway is the electrochemical hydrogen peroxide production, accomplished through the oxygen reduction reaction via a 2-electron pathway. This method not only simplifies the production process but also upholds environmental sustainability, especially when compared to the conventional anthraquinone method. In this review paper, recent works from the literature focusing on the 2-electron oxygen reduction reaction promoted by carbon electrocatalysts are summarized. The practical applications of these materials in the treatment of effluents contaminated with different pollutants (drugs, dyes, pesticides, and herbicides) are presented. Water treatment aiming to address these issues can be achieved through advanced oxidation electrochemical processes such as electro-Fenton, solar-electro-Fenton, and photo-electro-Fenton. These processes are discussed in detail in this work and the possible radicals that degrade the pollutants in each case are highlighted. The review broadens its scope to encompass contemporary computational simulations focused on the 2-electron oxygen reduction reaction, employing different models to describe carbon-based electrocatalysts. Finally, perspectives and future challenges in the area of carbon-based electrocatalysts for H2O2 electrogeneration are discussed. This review paper presents a forward-oriented viewpoint of present innovations and pragmatic implementations, delineating forthcoming challenges and prospects of this ever-evolving field.

cond-mat.mtrl-sci↗

Magnetic field-enhanced oxygen reduction reaction for electrochemical hydrogen peroxide production with different cerium oxide nanostructures

We investigated cerium oxide nanoparticles of various morphologies (nanosheets, nanocubes, and nanoparticles) supported on carbon Vulcan XC-72 for the two-electron oxygen reduction reaction (ORR). It was used a continuous magnetic field (2000 Oe) for the first time in the literature. The best results were for 5% (w/w) CeO2 for all three different morphologies, more than doubling the ring current, enhancing the hydrogen peroxide selectivity from 51% (Vulcan XC-72) to 84-89%, and modifying the onset potential to lesser negative values. The presence of the magnetic field led to even higher ring currents with 5% (w/w) CeO$_2$, H$_2$O$_2$ selectivity from 54% (Vulcan XC-72) to 88-96% and changing even more the onset potential. Those results were correlated with the Zeeman effect, the Lorentz force, generating magnetohydrodynamic effects, the Kelvin force, and the formation of Bound Magnetic Polarons. This pioneering research introduces an innovative approach, highlighting the potential of an external continuous magnetic field.

physics.chem-ph↗