Investigation into photocatalytic decolorisation of CI Reactive Black 5 using titanium dioxide nanopowder

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Abstract

The photocatalytic decolorisation of CI Reactive Black 5 using titanium dioxide nanopowder as a catalyst was studied and the results obtained are discussed in terms of its decolorisation efficiency. All experiments were performed using a double-walled quartz immersion well batch reactor in which the slurry form of the reactants was at its natural pH of 5.1. The performance of titanium dioxide nanopowder (size <25nm; surface area 200-220m 2/g) was compared with that of reference titanium dioxide powder (size ca. 230nm; surface area 11m 2/g); in both cases, the titanium dioxide samples were anatase. It was found that the photocatalytic decolorisation efficiencies obtained using titanium dioxide nanopowder were higher than those of the reference titanium dioxide powder, with the latter taking approximately 8min longer to achieve almost complete decolorisation of 10mg/l CI Reactive Black5. The photocatalytic decolorisation rate of CI Reactive Black5 using both titanium dioxide photocatalysts typically followed a first-order reaction and the decolorisation kinetics were successfully fitted to a simplified Langmuir-Hinshelwood kinetic model. In addition, the effects of light type and intensity, catalyst loading and initial CI Reactive Black5 concentration were investigated using titanium dioxide nanopowder as the photocatalyst in the decolorisation of the dye. This study shows that the recommended parameters for treating 10mg/l CI Reactive Black5 based on the experimental set-up and operating conditions are an ultraviolet light power of 125W (39.3mW/cm 2) and a 0.3-g/l catalyst loading. © 2011 The Authors. Coloration Technology © 2011 Society of Dyers and Colourists.

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Low, F. C. F., Wu, T. Y., Teh, C. Y., Juan, J. C., & Balasubramanian, N. (2012). Investigation into photocatalytic decolorisation of CI Reactive Black 5 using titanium dioxide nanopowder. Coloration Technology, 128(1), 44–50. https://doi.org/10.1111/j.1478-4408.2011.00326.x

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