SciELO - Scientific Electronic Library Online

 
vol.31 número3Evolución temporal de una depresión sobre la superficie del hielo monocristalino índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados

Revista

Articulo

Indicadores

  • No hay articulos citadosCitado por SciELO

Links relacionados

  • No hay articulos similaresSimilares en SciELO

Compartir


Anales (Asociación Física Argentina)

versión impresa ISSN 0327-358Xversión On-line ISSN 1850-1168

Resumen

CID, L. del C.; VERA, C. M. C.  y  SORICHETTI, P. A.. Photocatalytic activity of high-concentration Titanium Dioxide slurries at neutral pH. An. AFA [online]. 2020, vol.31, n.3, pp.77-85. ISSN 0327-358X.

The properties of high-concentration titanium dioxide slurries under UV irradiation were studied for photocatalytic oxidation of contaminants. Commercial nanoparticles of TiO2 (Evonik AeroxideÒ P25) at concentrations of 0.5, 1, 1.5, 2 and 2.5 g L-1 were irradiated by a mercury lamp (254 nm). At neutral pH, within the studied concentration range, nanoparticles form agglomerates of tens of micrometers. Their size, measured by optical microscopy, increases linearly with catalyst concentration. The attenuation length of the UV radiation was measured by a spectrophotometer with an integrating sphere. The concentration of the model contaminant (Orange II) was determined by spectrophotometry at intervals of 20 minutes, during the irradiation time (6 hours). The measured values fit satisfactorily to a pseudo first order kinetics. At catalyst concentrations of 1 g L-1 and higher, the kinetic constant is (8.1 ± 0.5) × 10-3 min-1. This is explained by the diminution of the attenuation length and the simultaneous increase of the total exposed surface at higher catalyst concentrations.

Palabras clave : agglomeration; high-concentration slurry; Orange II; photocatalysis; titanium dioxide.

        · resumen en Español     · texto en Español     · Español ( pdf )

 

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