Photocatalytic Degradation of Crystal Violet (CV) Dye over Metal Oxide (MO_x) Catalysts

Abstract

Crystal violet (CV) is an organic chloride salt and a triphenylmethane dye commonly used in the textile processing industry, also being used as a disinfectant and a biomedical stain. Although CV is widely used, it is carcinogenic to humans and is retained by industrial-produced effluent for an extended period. The different types of metal oxide (MOx) have impressive photocatalytic properties, allowing them to be utilized for pollutant degradation. The role of the photocatalyst is to facilitate oxidation and reduction processes by trapping light energy. In this study, we investigated different types of metal oxides, such as titanium dioxide (TiO2), zinc oxide (ZnO), zirconium dioxide (ZrO2), iron (III) oxide (Fe2O3), copper (II) oxide (CuO), copper (I) oxide (Cu2O), and niobium pentoxide (Nb2O5) for the CV decomposition reaction at ambient conditions. For characterization, BET and Raman spectroscopy were applied, providing findings showing that the surface area of the anatase TiO2 and ZnO were 5 m2/g and 12.1 m2/g, respectively. The activity tests over TiO2 and ZnO catalysts revealed that up to ~98% of the dye could be decomposed under UV irradiation in x, the band gap–water splitting relationship, and the recombination rate of electron holes.

Keywords

• band gap
• crystal violet
• heterogenous catalyst
• photocatalysis
• recombination rate
• water splitting