Comparing the efficacy of catalytic ozonation and photocatalytical degradation of cyanide in industrial wastewater using ACF-TiO2: catalyst characterisation, degradation kinetics, and degradation mechanism

Abstract

ABSTRACTIn the present study, the ACF-TiO2 catalyst was synthesised and used as a catalyst for the destruction of toxic cyanide in both synthetic and real industrial wastewaters. The ACF-TiO2 catalyst was found to be micro-porous with the BET surface area of 163 m2/g. The effect of different operational parameters such as catalyst concentration, cyanide concentration, operation time, and ozone concentration were target parameters in the present study. The findings show that 500 mg/L of catalyst is the optimum value for the photocatalytical process to completely oxidise 25 mg/L of cyanide within 10 min. While it was found that 300 mg/L of catalyst in the presence of 200 mg/h ozone is enough to remove 25 mg/L cyanide within operation time of 24 min. Degradation of the cyanide in both investigated processes follow the pseudo-first-order kinetic and the reaction rate constant is almost 2 times higher in the photocatalytical process compared with catalytic ozonation process. Furthermore, the quenching tests using salicylic acid demonstrated the hydroxyl radical generation in the investigated process. Generation of highly oxidising hydroxyl radical makes the photocatalytical process a promising process for the transformation of noxious cyanide to much less toxic compounds (ammonia and nitrate). Accordingly, it can be concluded that ACF-TiO2 could be a catalyst for degradation and detoxification of cyanide.