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Bruno L. Batista

Publications and source records attributed to Bruno L. Batista.

3 recordsLinked to original sources

Fe3O4 Nano-octahedra/Vulcan XC72: Optimization and Combination with Solar-Based Electro-Fenton for Progestins Degradation

The widespread presence of synthetic progestins, such as levonorgestrel (LNG) and gestodene (GES), in aquatic environments poses significant ecotoxicological risks due to their endocrine-disrupting properties. In this study, nano-octahedral magnetite (Fe3O4-NO) was synthesized via a hydrothermal route and incorporated into gas diffusion electrodes (GDEs) supported on Vulcan XC72 to enhance the in-situ electrogeneration of hydrogen peroxide (H2O2). High-resolution transmission electron microscopy, X-ray diffraction, SEM, X-ray photoelectron spectroscopy, and contact angle measurements thoroughly characterized the physicochemical and morphological properties of the materials. The 3% Fe3O4-NO/C catalyst provided a two-fold increase in H2O2 selectivity compared with Vulcan XC72. Electrochemical performance was optimized using a 2^3 factorial design and principal component analysis (PCA), with current density, pH, and Na2SO4 concentration as variables. The optimized GDE (3% Fe3O4-NO/C) achieved a maximum H2O2 production of 0.44 +/- 0.02 g L-1 with a current efficiency of 43.1 +/- 0.23% and a specific energy consumption of 0.012 +/- 0.009 kWh g-1. The electrode was further applied to the degradation of LNG and GES using solar and anodic-assisted electro-Fenton processes. Under optimal conditions, over 70% removal of both progestins was achieved, with stable performance across three operational cycles. These findings demonstrate the potential of 3% Fe3O4-NO/C-GDEs as efficient, reusable cathodes for sustainable electrochemical advanced oxidation processes (EAOPs) in water treatment.

physics.chem-ph

Fe3O4 nano-octahedra and SnO2 nanorods modifying low-Pd amount electrocatalysts for alkaline direct ethanol fuel cells

This work describes the ethanol oxidation reaction (EOR) in alkaline medium using low-palladium nanoparticle electrocatalysts modified by Fe3O4 nano-octahedra and SnO2 nanorods. Operation studies on an alkaline direct ethanol fuel cell (ADEFC) were conducted using the developed electrocatalysts, and stability studies were performed using the advanced scanning flow cell (SFC) technique coupled to inductively coupled plasma mass spectrometry (online SFC-ICP-MS). The EOR was catalyzed by single (Pd/C and commercial Pd/C Alfa Aesar) and by synthesized binary and ternary electrocatalysts, in which Fe3O4 and SnO2 nanostructures partially replaced the high-cost noble metal. The PdFe3O4/C was identified as the most promising synthesized material in the electrochemical studies, exhibiting the highest mass activity (1426 mA mg-1 Pd) by cyclic voltammetry (CV), followed by the binary PdSnO2/C (1135 mA mg-1 Pd), and by the ternary (1074 mA mg-1 Pd). This enhancement was attributed to the bifunctional mechanism enabled by Fe3O4 and SnO2, therefore reducing poisoning and improving the EOR. Moreover, the operating results revealed that PdFe3O4/C showed the highest power density among the synthesized materials (31 mW cm-2 at 70 C), even with an approximately 45 percent reduction in Pd content compared to the commercial catalyst. XPS results showed that the Pd 3d5/2 and 3d3/2 peaks for PdFe3O4/C, PdSnO2/C, and PdFe3O4SnO2/C were shifted by approximately 0.5 eV to higher binding energies compared to Pd/C, indicating a loss of electron density in Pd due to strong metal-oxide interactions.

cond-mat.mtrl-sci

Stability of Supported Pd-based Ethanol Oxidation Reaction Electrocatalysts in Alkaline Media

This study evaluates the dissolution of the supported electrocatalysts Pd/C, PdSn/C, PdNb/C, and PdFe3O4/C during ethanol oxidation reaction for ADLFC applications. A scanning flow cell (SFC) coupled to an inductively coupled mass spectrometry (online ICP-MS) is used to assess the dissolution stability in a broad potential window. Accelerated stress tests with and without ethanol are developed using a rotating disk electrode (RDE) with dissolution products analysis by ex-situ ICP-MS. Potential profiles simulating those experienced by the catalyst during regular fuel cell operation were used. Sn and Fe catalysts demonstrate improved activity and stability compared with the material with Pd alone. For these reasons, PdSn/C and PdFe3O4/C are suitable for ADLFC applications. Severe Nb dissolution destabilizes Pd, increasing its leaching. This work demonstrates that while additional metals and oxides can improve the alcohol oxidation kinetics of Pd, these additives' dissolution stability must already be considered at the catalyst design stage.

cond-mat.mtrl-sci