SciELO - Scientific Electronic Library Online

 
vol.24 número2Around voltammetry: from colouring matters to beerThe effects of soluble salts at the metal/paint interface: advances in knowledge índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados

Revista

Articulo

Indicadores

Links relacionados

  • No hay articulos similaresSimilares en SciELO

Compartir


Portugaliae Electrochimica Acta

versión impresa ISSN 0872-1904

Resumen

BRILLAS, E. et al. Degradation of organic contaminants by advanced electrochemical oxidation methods. Port. Electrochim. Acta [online]. 2006, vol.24, n.2, pp.159-189. ISSN 0872-1904.

Advanced electrochemical oxidation processes (AEOPs) constitute promising technologies for the treatment of organic pollutants in waters. They are based on the production of oxidant hydroxyl radical (·OH) from water oxidation on the surface of a high O2-overvoltage anode and/or from Fenton’s reaction between added Fe2+ and hydrogen peroxide electrogenerated at the cathode by two-electron O2 reduction. In this paper, fundamentals of AEOPs such as anodic oxidation, electro-Fenton, photoelectro-Fenton and peroxi-coagulation are described, and comparative degradation of aqueous solutions with aromatic pollutants, such as aniline, 4-chlorophenol and several chlorophenoxyacetic and chlorobenzoic acids, in 0.05 M Na2SO4 + H2SO4 of pH 3.0 by these techniques using an undivided electrolytic cell with an O2-diffusion cathode under galvanostatic conditions is discussed. The decay kinetics of chlorophenoxyacetic acids and the evolution of their aromatic intermediates and generated carboxylic acids are also reported to clarify their mineralization processes by the different AEOPs. Anodic oxidation with a Pt anode yields poor decontamination of pollutants, while alternative anodic oxidation with a boron-doped diamond (BDD) anode leads to total mineralization of all solutions due to the greater production of ·OH on the BDD surface. Electro-Fenton with a Pt anode has high oxidation ability at short electrolysis times, but the formation of stable Fe3+-oxalate complexes limits the degradation of aromatic contaminants. These products are completely oxidized in electro-Fenton with a BDD anode or photodecomposed by the action of UVA light in photoelectro-Fenton with a Pt anode. Peroxi-coagulation with an Fe anode also gives fast degradation with generation of small amounts of stable Fe3+ complexes, since organics are mainly retained in the Fe(OH)3 precipitate formed.

Palabras clave : anodic oxidation; boron-doped diamond electrode; electro-Fenton; photoelectro-Fenton; peroxi-coagulation.

        · texto en Inglés     · Inglés ( pdf )

 

Creative Commons License Todo el contenido de esta revista, excepto dónde está identificado, está bajo una Licencia Creative Commons