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Kinetics and Isotherm Study of Ceftriaxone Removal Using Functionalized Biochar Combined with Photocatalysis
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Resumo(s)
The increasing presence of antibiotics such as cephalosporins in wastewater represents a significant environmental risk. These compounds are excreted in large quantities, and conventional wastewater treatment plants are often ineffective at their removal. Consequently, the development of more sustainable and efficient treatment technologies is essential. In this study, the removal of cephalosporins from aqueous solutions was evaluated through adsorption using pine bark biochar, photocatalysis with TiO2, and a combination of both processes. Kinetic experiments were conducted with cephalosporin solutions (15 mg/L), employing 150 mg/L of biochar, 100 mg/L TiO2, or their combination, under continuous stirring and/or UV-vis irradiation. Samples were collected at 0 and 120 min and analyzed via UV-vis spectrophotometry. Adsorption isotherms were established for initial cephalosporin concentrations ranging from 5 to 50 mg/L. The biochar alone achieved a removal efficiency of 94.2% after 120 min. Photocatalysis with TiO2 alone resulted in 75% removal, while the combined approach reached 95.9%, indicating a synergistic effect between adsorption and photodegradation mechanisms. Kinetic data fitted the pseudosecond-order model, and the Langmuir isotherm provided the best correlation, suggesting monolayer adsorption. These findings demonstrate that pine bark biochar, whether used independently or in combination with TiO2, constitutes an eco-friendly, effective, and low-cost alternative for the removal of antibiotics from wastewater, while simultaneously contributing to the valorization of forestry residues
Descrição
Palavras-chave
antibiotic ceftriaxone sodium cephalosporins biochar photocatalysis wastewater treatment
Contexto Educativo
Citação
Cruz-Lopes, L.; Araújo, R.; Lopes, A.R.; Moles, S.; Romero-Sarria, F.; Esteves, B. Kinetics and Isotherm Study of Ceftriaxone Removal Using Functionalized Biochar Combined with Photocatalysis. Molecules 2025, 30, 4291. https://doi.org/10.3390/ molecules30214291