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Photocatalytic degradation of methylene blue and phenol on Fe-doped sulfated titania

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Abstract

Fe-doped sulfated titania (FST) photocatalysts with high photocatalytic activity were prepared from industrial titanyl sulfate solution and characterized using X-ray diffraction (XRD), thermogravimetry analysis–differential scanning calorimeter (TGA-DSC), Fourier transform infrared spectroscopy (FT-IR), and nitrogen adsorption–desorption techniques. The photocatalytic activity of the FST photocatalyst was evaluated using the photodegradation of methylene blue (MB) and the photooxidation of phenol in aqueous solutions in the presence of UV irradiation, respectively. The effect of various parameters, such as calcining temperature, calcination time, initial concentration of substrate, amount of catalyst and pH value on the photocatalytic activity of FST photocatalyst was investigated. Among the parameters studied, calcining temperature, initial concentration of substrate, and amount of catalyst have a very similar effect on the activity of FST photocatalyst for both the photodegradation of MB and the photooxidation of phenol, while the others have distinct differences. The optimal calcination conditions were 500 °C, 1.5 h and 650 °C, 2.5 h; the optimal catalyst concentration were 1.0 and 1.2 g L−1; the optimal pH values were 8 and 4 for the photodegradation of MB and the photooxidation of phenol, respectively. In addition, the mechanism for the high photocatalytic efficiency of FST photocatalyst has also been put forward.

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Acknowledgments

This study was supported by the National Natural Science Foundation of China (50804025), the Applied and Basic Research Program of Sichuan Province, China (2008JY0140), the Youths Foundation of Sichuan Province, China (09ZQ026-067), the Talents Innovation Project of Panzhihua City, China (2009TX-5(1)) and the Promoting Industrialization Program of Panzhihua City, China (2011CY-G-23).

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Yang, Y., Tian, C. Photocatalytic degradation of methylene blue and phenol on Fe-doped sulfated titania. Res Chem Intermed 38, 693–703 (2012). https://doi.org/10.1007/s11164-011-0409-5

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