Dynamics of Diffusion- and Immobilization-Limited Photocatalytic Degradation of Dyes by Metal Oxide Nanoparticles in Binary or Ternary Solutions

Abstract

Photocatalytic degradation employing metal oxides, such as TiO2 nanoparticles, as catalysts is an important technique for the removal of synthetic dyes from wastewater under light irradiation. The basic principles of photocatalysis of dyes, the effects of the intrinsic photoactivity of a catalyst, and the conventional non-fundamental factors are well established. Recently reported photocatalysis studies of dyes in single, binary, and ternary solute solutions opened up a new perspective on competitive photocatalytic degradation of the dyes. There has not been a review on the photocatalytic behavior of binary or ternary solutions of dyes. In this regard, this current review article summarizes the photocatalytic behavior of methylene, rhodamine B, and methyl orange in their binary or ternary solutions. This brief overview introduces the importance of the dynamics of immobilization and reactivity of the dyes, the vital roles of molecular conformation and functional groups on their diffusion onto the catalyst surface, and photocatalytic degradation, and provides an understanding of the simultaneous photocatalytic processes of multiple dyes in aqueous systems.