Abstract

Photocatalysis, electrolysis, water jet cavitation (WJC), alone and in combinations were applied to degrade an azo dye, Reactive Brilliant Red X-3B (X-3B). Experiments were conducted in a 4.0L aqueous solution with different initial dye concentrations, TiO2 dose, and solution pH. WJC substantially increased the photocatalytic, electrolytic and photocatalytic–electrolytic rates of the dye removal. The observed first-order rate of X-3B decolorization in the process of combined photocatalysis and electrolysis coupled with WJC was 1.6–2.9 times of that in the process of combined photocatalysis and electrolysis coupled with mechanical stirring. The rate enhancements may be attributed primarily to the reduced diffusion layer thickness on the electrodes and the deagglomeration of photocatalyst particles due to the chemical and physical effects of WJC. Under the conditions of 80mg/L X-3B solution, 100mg/L TiO2 dose and solution pH 6.3, 97% and 71% of color and chemical oxygen demand (CODCr) were removed, respectively, within 90-min photocatalytic–electrolytic treatment coupled with WJC. During this process, azo groups and naphthalene, benzene and triazine structures of the dye can be destroyed. Industrial textile effluent was also investigated, and a positive synergistic effect between photocatalytic–electrolytic system and WJC was observed considering color removal.

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