RESUMO
In this work, we fabricated a TiO2 thin film, and the same film was modified with an Anderson aluminum polyoxometalate (TiO2-AlPOM). Physical-chemical characterization of the catalysts showed a significant change in morphological and optical properties of the TiO2 thin films after surface modification. We applied the kinetic and isothermal models to the methylene blue (MB) adsorption process on both catalysts. The pseudo-second order model was the best fitting model for the kinetic results; qe (mg/g) was 11.9 for TiO2 thin films and 14.6 for TiO2-AlPOM thin films, and k2 (g mg-1 min-1) was 16.3 × 10-2 for TiO2 thin films and 28.2 × 10-2 for TiO2-AlPOM thin films. Furthermore, the Freundlich model was suitable to describe the isothermal behavior of TiO2, KF (5.42 mg/g), and 1/n (0.312). The kinetics of photocatalytic degradation was fitted using the Langmuir-Hinshelwood model; kap was 7 × 10-4 min-1 for TiO2 and 13 × 10-4 min-1 for TiO2-AlPOM. The comparative study showed that TiO2 thin films reach a 19.6% MB degradation under UV irradiation and 9.1% MB adsorption, while the TiO2-AlPOM thin films reach a 32.6% MB degradation and 12.2% MB adsorption on their surface. The surface modification improves the morphological, optical, and photocatalytic properties of the thin films. Finally, the DFT study supports all the previously shown results.
RESUMO
In this work, we fabricated and characterized ZnO and TiO2 thin films, determining their structural, optical, and morphological properties. Furthermore, we studied the thermodynamics and kinetics of methylene blue (MB) adsorption onto both semiconductors. Characterization techniques were used to verify thin film deposition. The semiconductor oxides reached different removal values, 6.5 mg/g (ZnO) and 10.5 mg/g (TiO2), after 50 min of contact. The pseudo-second-order model was suitable for fitting the adsorption data. ZnO had a greater rate constant (45.4 × 10-3) than that of TiO2 (16.8 × 10-3). The removal of MB by adsorption onto both semiconductors was an endothermic and spontaneous process. Finally, the stability of the thin films showed that both semiconductors maintained their adsorption capacity after five consecutive removal tests.
RESUMO
In this work, we studied the methylene blue (MB) dye adsorption capacity on biochar derived from residues of Prosopis juliflora seed waste, a species found in the region of the tropical dry forest of Piojó in the Department of Atlántico, Colombia. The materials were obtained by pyrolysis at temperatures of 300, 500, and 700 °C. Biochar was characterized using Fourier transform infrared (FTIR), scanning electron microscopy and energy-dispersive X-ray spectroscopy (SEM-EDX), TGA, and Brunauer-Emmett-Teller (BET) techniques. The three biochar samples presented a macroporous, rough structure with pore size between 6 and 28 µm. The largest pore surface area observed was 1.28 m2/g for pyrolyzed biochar produced at 500 °C, larger than that of biochar produced at 700 °C, which was 0.83 m2/g. The adsorption results show that the maximum percentage of MB removal was 69%. According to SEM results, the material's pore sizes varied on average from 6 to 28 µm. We modeled MB adsorption on biomass through three different isotherm models. The Freundlich model was the best-fitting model for the removal of MB (K F = 1.447; 1/n = 0.352). The kinetic results showed that the pseudo-second-order model was the best-fitting model for the sorption process (q e = 2.94 mg/g; k 2 = 0.087 g/(mg/min-1)). Furthermore, the recycling test showed that the biochar did not change its adsorption capacity significantly. Finally, under the experimental conditions, the thermodynamic parameters indicated that the removal of MB using biochar was an endothermic and spontaneous process; all ΔG° values ranged from -2.14 to -0.95 kJ/mol; ΔH° was 23.54 kJ/mol and ΔS° was 79.5 J/mol.