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Degradation of acetic acid with sulfate radical generated by persulfate ions photolysis
Authors:Justine Criquet  Nathalie Karpel Vel Leitner  
Institution:aLaboratoire de Chimie et Microbiologie de l’Eau – UMR CNRS 6008, Ecole Supérieure d’Ingénieurs de Poitiers, Université de Poitiers, 40, av du recteur Pineau, 86022 POITIERS Cedex, France
Abstract:The photolysis of View the MathML source was studied for the removal of acetic acid in aqueous solution and compared with the H2O2/UV system. The View the MathML source radicals generated from the UV irradiation of View the MathML source ions yield a greater mineralization of acetic acid than the radical dotOH radicals. Acetic acid is oxidized by View the MathML source radicals without significant formation of intermediate by-products. Increasing system pH results in the formation of radical dotOH radicals from View the MathML source radicals. Maximum acetic acid degradation occurred at pH 5. The results suggest that above this pH, competitive reactions with the carbon mineralized inhibit the reaction of the solute with View the MathML source and also radical dotOH radicals. Scavenging effects of two naturally occurring ions were tested; in contrast to View the MathML source ions, the presence of Cl ions enhances the efficiency of the View the MathML source/UV process towards the acetate removal. It is attributed to the formation of the Clradical dot radical and its great reactivity towards acetate.
Keywords:Sulfate radical  Mineralization  Carboxylic acids  Persulfate  Photolysis
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