Huge water consumptions and pollutants releases in the environment urge effective water decontamination technologies, fostering extensive recycle and reuse of industrial process-water and wastewater. The heterogeneous catalytic wet air oxidation (CWAO) offers a practical solution to the problem of decontamination of industrial effluents characterised by high concentration of toxic-refractory compounds, which are also detrimental for the active sludge of biological systems. Therefore, this work shows the superior CWAO performance of a new class of nanostructured MnCeOx catalysts toward the mineralization of some common toxic and refractory industrial pollutants. Mechanistic and kinetic evidences are summarised into a Langmuir-Hinshelwood reaction mechanism, leading to a formal kinetic model predicting the CWAO performance of nanostructured MnCeOx catalysts and optimum reaction conditions.

Catalytic Wet Air Oxidation (CWAO) of Industrial Wastewaters: Mechanistic Evidences, Catalyst Development and Kinetic Modeling

F. Arena
Membro del Collaboration Group
;
R. Di Chio
Membro del Collaboration Group
;
C. Espro
Membro del Collaboration Group
;
2017-01-01

Abstract

Huge water consumptions and pollutants releases in the environment urge effective water decontamination technologies, fostering extensive recycle and reuse of industrial process-water and wastewater. The heterogeneous catalytic wet air oxidation (CWAO) offers a practical solution to the problem of decontamination of industrial effluents characterised by high concentration of toxic-refractory compounds, which are also detrimental for the active sludge of biological systems. Therefore, this work shows the superior CWAO performance of a new class of nanostructured MnCeOx catalysts toward the mineralization of some common toxic and refractory industrial pollutants. Mechanistic and kinetic evidences are summarised into a Langmuir-Hinshelwood reaction mechanism, leading to a formal kinetic model predicting the CWAO performance of nanostructured MnCeOx catalysts and optimum reaction conditions.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11570/3121536
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