Treatment of leachate waters by wet peroxide oxidation with a compost-based catalyst: effect of pH

• Autor(a) principal: Batista, Gabriel de Freitas
• Data de Publicação: 2021
• Outros Autores: Roman, Fernanda, Díaz de Tuesta, Jose Luis, Mambrini, Raquel Vieira, Gomes, Helder
• Idioma: eng
• Título da fonte: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
• Texto Completo: http://hdl.handle.net/10198/27236
• topic: pH; H2O2

A compost-based catalyst was synthesized by hydrothermal carbonization following the procedure described elsewhere1 (3 g of compost in 30 mL of water, 230 °C for 2 h). The material was assessed in the catalytic wet peroxide oxidation (CWPO) of a leachate water, generated during an anaerobic digestion of municipal solid waste. The leachate water is characterized by a high pollutant load (chemical oxygen demand, COD, of 60 g L-1 and total organic carbon, TOC, of 27 g L-1). The CWPO runs were conducted at initial pH (pH0) of 3 and 6, and at the natural pH of the effluent (7.2), Ccatalyst = 1.8 g L-1, 80 °C, and the stoichiometric concentration of H2O2 needed to mineralize the organic content (based on COD). Fig. 1 shows the results obtained along the reaction. An acidic pH (pH0 = 3) resulted in a more controlled, but also incomplete, consumption of H2O2, leading to a low conversion of COD and TOC (20 and 10%, respectively). Contrarily, the natural pH led to a very fast and uncontrolled consumption of the oxidant source, resulting in 100% decomposition of H2O2 in less than 2 h of reaction, but failing to remove COD or TOC (negligible removal, ca. 0%), ascribed to parasitic reactions occurring by the inefficient consumption of H2O2. At pH0 = 6, an intermediate behavior was observed: complete decomposition of H2O2 was possible, at a more controlled rate compared to the natural pH. The result was an increment in COD (41%) and TOC removals (19%), almost two times than that observed at the pH0 3.