Artículo
Adsorption of paraquat on mesoporous silica modified with titania: Effects of pH, ionic strength and temperature
Fecha de publicación:
11/2011
Editorial:
Academic Press Inc Elsevier Science
Revista:
Journal of Colloid and Interface Science
ISSN:
0021-9797
Idioma:
Inglés
Tipo de recurso:
Artículo publicado
Clasificación temática:
Resumen
The adsorption of the herbicide paraquat (PQ 2+) on the binary system titania-silica has been studied in batch experiments by performing adsorption isotherms under different conditions of pH, supporting electrolyte concentration, and temperature. Adsorption kinetic on the studied material has also been carried out and discussed. PQ 2+ adsorption is very low on the bare silica surface but important on the composed TiO 2-SiO 2 adsorbent. In this last case, the adsorption increases by increasing pH and decreasing electrolyte concentration. There are no significant effects of temperature on the adsorption. The increase of the adsorption in TiO 2-SiO 2 seems to be related to an increase in acid sites of the supported titania and to the homogenously dispersion of the TiO 2 nanoparticles over the silica support. The adsorption takes place by direct binding of PQ 2+ to TiO 2 leading to the formation of surface species of the type SiO 2-TiO 2-PQ 2+. Electrostatic interactions and charge-transfer and outer-sphere complexes formations seem to play a key role in the adsorption mechanism. The analysis of thermodynamic parameters suggests that the adsorption on TiO 2-SiO 2 is endothermic and spontaneous in nature. © 2011 Elsevier Inc.
Palabras clave:
Adsorption
,
Paraquat
,
Silica
,
Solid-Water Interface
,
Surface Complexes
,
Titania
Archivos asociados
Licencia
Identificadores
Colecciones
Articulos(INQUISUR)
Articulos de INST.DE QUIMICA DEL SUR
Articulos de INST.DE QUIMICA DEL SUR
Citación
Brigante, Maximiliano Eduardo; Schulz, Pablo Carlos; Adsorption of paraquat on mesoporous silica modified with titania: Effects of pH, ionic strength and temperature; Academic Press Inc Elsevier Science; Journal of Colloid and Interface Science; 363; 1; 11-2011; 355-361
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