Elsevier

Solar Energy

Volume 70, Issue 4, 2001, Pages 331-337
Solar Energy

Photocatalytic degradation of organic compounds in aqueous solution by a TiO2-coated rotating-drum reactor using solar light

https://doi.org/10.1016/S0038-092X(00)00139-0Get rights and content

Abstract

This paper deals with the degradation of aqueous phenol by a newly proposed rotating-drum reactor coated with a TiO2 photocatalyst, in which TiO2 powders loaded with Pt are immobilized on the outer surface of a glass-drum. The reactor can receive solar light and oxygen from the atmosphere effectively. It was shown experimentally that phenol can be decomposed rapidly by this reactor under solar light: with our experimental conditions the phenol with an initial concentration of 22.0 mg/dm3 was decomposed within 60 min and was completely mineralized through intermediate products within 100 min. The photonic efficiency under solar light was shown to take the value 0.00742 mol-C/Einstein. The photocatalytic decomposition processes of phenol by this reactor were also discussed on the basis of the Langmuir–Hinshelwood kinetic model.

Introduction

Photocatalytic oxidation reactions have the potential to completely mineralize organic compounds to carbon dioxide by solar light and to lead us to a ‘clean and green purification technology’ for treatment of polluted air and water (Ollis and Al-Ekabi, 1993, Parent et al., 1996). Several semiconductors such as TiO2, Fe2O3, ZnO, ZnS, CdS, WO3 are known to have photocatalytic properties (Domènech, 1993, Hasegawa and Mayo, 1986, Lepore et al., 1993). Among them, TiO2 is the most widely used for its high photocatalytic activity, stability and non-toxicity (Nogueira and Jardim, 1996, Okamoto et al., 1985).

For air purification, some practical purification technologies using the TiO2 photocatalyst have been achieved. For water purification, however, viable applications have not been realized yet, in spite of extensive basic research related to the decomposition of aqueous organic pollutants by a TiO2 photocatalyst. In existing publications, the reactors with suspension of TiO2 powder have been widely researched; in these reactors the water has to be continuously stirred during the reaction and the TiO2 powder has to be separated from the treated water. In contrast to the powder, the film type photocatalyst with immobilized TiO2 powder is attractive as it avoids such disadvantages.

The main purpose of the present study is to develop a new photocatalyst reactor for water purification which can be operated under solar light. We here propose a rotating-drum reactor coated with a TiO2 photocatalyst, in which Pt-loaded TiO2 powder is immobilized on the outer surface of a glass-drum. The reactor can receive solar light and oxygen from the atmosphere effectively: since the water film on the drum is very thin, the light can easily penetrate to the TiO2 surface and O2 in the atmosphere can diffuse rapidly to the TiO2 surface, which leads to a rapid production of ·OH and ·OOH radicals.

The reactor was tested by decomposing aqueous phenol under solar light and its performance was evaluated. It was shown that phenol can be decomposed effectively by this reactor under solar light. The experiment using artificial ultraviolet light was also carried out and the results were compared with those obtained using solar light. The degradation and mineralization processes were also shown to be explained by the Langmuir–Hinshelwood kinetic model.

Section snippets

Pretreatment of TiO2 powder

We used an anatase type of titanium dioxide powder (TP-2, Fuji Titanium Ltd.) of 0.15 μm mean diameter for the photocatalyst. To improve the photocatalytic activity, we loaded platinum on the surface of the TiO2 powder in accordance with the method proposed by Kraeutler and Bard (1978). 18.5 g TiO2 powder was dispersed in 1 dm3 aqueous solution of 0.50 g/dm3 hexachloroplatinic acid, H2[PtCl6]·6H2O (GR, Katayama Ltd.) and 0.22 g/dm3 methanol, CH3OH (GR, Katayama Ltd.). The solution was

Decomposition of phenol by solar light

Fig. 3 shows the variations of phenol and TOC concentrations with illumination time in process of degradation when the reactor is operated under solar light. The radiation power density of the solar ultraviolet band between 305 and 395 nm, which was measured simultaneously, is also shown with the dashed line in the figure. The radiation power density of the light lies within 25 and 32 W/m2. As seen in the figure, phenol is degraded unexpectedly fast: the concentration decreases from 22.0 to 0

CONCLUSION

In this paper, a rotating-drum reactor coated with a TiO2 photocatalyst is proposed. The performance of the reactor is evaluated by decomposing aqueous phenol and the photocatalytic reaction process is discussed. The results can be summarized as follows.

  • 1.

    The double-layer film of Pt-loaded TiO2 film/water glass fabricated in this research is very stable and exhibits high photocatalytic activity. The TiO2-coated rotating-drum reactor can effectively purify the water containing organic substances.

  • 2.

Acknowledgements

The authors are indebted to Dr. Y. Kawashima at Himeji Institute of Technology for providing data on the radiation power density of solar light in Harima district.

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