This study describes the synthesis of an innovative nanomaterial (patent application number BR 1020210000317) composed of cobalt ferrite functionalized in niobium pentoxide CoFe₂O₄@Nb₅O₂ (CFNb), synthesized via green synthesis using tangerine peel extract. The material emphasizes the combination of a magnetic material (which allows for easy recovery after application) with niobium pentoxide (a metal which is abundant in Brazil). CFNb was applied as a catalyst for the paracetamol (PCT) degradation by photocatalysis. The new materials were characterized through surface and pore analysis (S_BET, S_EXT, S_mic, V_mic, and V_TOTAL), photoacoustic spectroscopy (PAS), zero charge point (pH_PZC, scanning electron microscopy (SEM/EDS), and X-ray diffraction (XRD). The reaction parameters studied included pH and catalyst concentration. The results indicated that the CFNb nanocatalysts were efficient in the paracetamol degradation, presenting better results in conditions of low pH (close to 2) and low catalyst concentration under irradiation of the 250 W mercury vapor lamp (greater than 28 mW·cm⁻²) at 60 min of reaction.

TiO₂-based semiconductors are formidable photocatalysts for redox reaction applications. Although N-doped TiO₂-Nb₂O₅ catalysts have already been explored in the literature, studies on their antioxidant activity are scarce, and systematic investigations on the effects of synthesis parameters over a wide range of %Nb and NH₄OH concentrations are limited. In addition, the relationship between optimal pH and %Nb has not yet been adequately explored. In the present work, the sol–gel synthesis of N-doped TiO₂-Nb₂O₅ catalysts was optimized using a design of experiments approach focused on photocatalysis, adsorption, and antioxidant applications. The samples were characterized by TGA, SEM/EDS, XRD, PZC tests, photoacoustic spectroscopy, and N₂-adsorption/desorption experiments. The salicylic acid (SA) degradation tests and DPPH radical scavenging assays demonstrated the superior photocatalytic activity (up to 72.9% SA degradation in 30 min, pH 5) and antioxidant capacity (IC₅₀ = 88.9 μg mL⁻¹) of pure TiO₂ compared to the N-doped TiO₂-Nb₂O₅ catalysts. The photocatalytic activity, however, proved to be intensely dependent on the pH and %Nb interaction, and at pH 3, the 25Nb-1N-400 catalyst promoted more significant SA degradation (59.9%) compared to pure TiO₂ (42.8%). In the methylene blue (MB) adsorption tests, the catalysts N-doped TiO₂-Nb₂O₅ showed removals at least seven times greater than TiO₂ catalysts without Nb.

The present work explored the adsorptive capacity and catalytic activity of rock powders from basaltic and granitic rocks in the discoloration of synthetic and industrial effluents containing the yellow dye Basic Yellow 96. The rock powders were characterized with scanning electron microscopy associated with energy-dispersive spectroscopy, photoacoustic spectroscopy, N₂ physisorption and X-ray diffraction, the latter confirming the abundant presence of silica in the four materials studied. The basaltic powders presented specific surface areas between 7 and 10 times greater than those of granitic materials, which allowed up to 92% removal of the dye in 3 h of test using the basaltic powder. Despite the smaller area, the granitic materials showed considerable photocatalytic activity in 3 h, 94%, the same as that of the basaltic materials in the photocatalysis. Granitic and basaltic photocatalysts proved to be efficient in the discoloration of synthetic and industrial effluents, although TOC analyses indicated that it was not possible to promote the pollutant mineralization in the industrial effluent. Both artificial light and sunlight were effective in the photocatalysis of the dye, although the former was slightly faster.

In the present work, rock dust was evaluated as an adsorbent and heterogeneous photocatalyst in the discoloration of Basazol Yellow 46 L dye, which is widely used in the dyeing of molded pulp packages. Although rock dust is produced in large quantities in quarries as a byproduct of rock exploration, little is known about its application as a photocatalyst. Rock dust was characterized by XRD, SEM/EDS, photoacoustic spectroscopy, and N₂ physisorption and had its photocatalytic activity assessed through phenol and salicylic acid degradation tests. The characterization results showed that the rock dust is mainly composed of silica and alumina in a triclinic structure, has a bandgap energy of 2.36 eV, and has a specific area of 1.5 m²/g. Rock dust was proven to be photocatalytically active in phenol and salicylic acid degradation tests and also presented the adsorptive and photocatalytic capacity for the discoloration of effluent containing Basazol Yellow 46 L dye.