Treatment of real winery wastewater by wet oxidation at mild temperature

This study explores the treatment of high-strength real winery wastewater (COD0 ≈ 35 g/L, TOC0 ≈ 11 g/L) by wet oxidation processes. Wet air oxidation (WAO), catalytic wet air oxidation (CWAO), H 2O2-promoted CWAO, wet peroxide oxidation (WPO) and catalytic wet peroxide oxidation (CWPO) were the opt...

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Detalles Bibliográficos
Autores: Domínguez Torre, Carmen María, Quintanilla Gómez, María Asunción, Casas de Pedro, José Antonio, Rodríguez Jiménez, Juan José
Tipo de recurso: artículo
Fecha de publicación:2014
País:España
Institución:Universidad Autónoma de Madrid
Repositorio:Biblos-e Archivo. Repositorio Institucional de la UAM
Idioma:inglés
OAI Identifier:oai:repositorio.uam.es:10486/710326
Acceso en línea:http://hdl.handle.net/10486/710326
https://dx.doi.org/10.1016/j.seppur.2014.04.003
Access Level:acceso abierto
Palabra clave:Ecotoxicity
Carbon Catalysts
Catalytic Wet Air Oxidation
Catalytic Wet Peroxide Oxidation
Winery Wastewater
Química
Descripción
Sumario:This study explores the treatment of high-strength real winery wastewater (COD0 ≈ 35 g/L, TOC0 ≈ 11 g/L) by wet oxidation processes. Wet air oxidation (WAO), catalytic wet air oxidation (CWAO), H 2O2-promoted CWAO, wet peroxide oxidation (WPO) and catalytic wet peroxide oxidation (CWPO) were the options tested using different carbon-based catalysts, viz. activated carbon, carbon black and graphite. Their suitability was analyzed in terms of polyphenol, chemical oxygen demand (COD) and total organic carbon (TOC) abatement upon 4 h reaction time. The results showed that hydrogen peroxide was the unique oxidant capable of achieving an effective reduction of the organic load. The graphite tested was the most active catalyst, most probably due in great part to its Fe content (0.4 wt.%), resistant to leaching. CWPO with that graphite was tested at different conditions following the evolution of COD, TOC and ecotoxicity. The best results were obtained by using graphite at 5 g/L, the original pH of the wastewater (3.8), 125 °C and the stoichiometric amount of hydrogen peroxide distributed in stepwise additions. Under those conditions, 80% COD and TOC removals with 85% of hydrogen peroxide efficiency were achieved after 4 h reaction time, giving rise to colorless effluents of very low Microtox ecotoxicity