Title of article :
Preparation and characterization of PVA–I complex doped mesoporous TiO2 by hydrothermal method
Author/Authors :
Rong-qian Shi، نويسنده , , Caiyun Jiang، نويسنده , , Yuping Wang، نويسنده , , Weiben Yang، نويسنده , , Chun Yang، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2013
Pages :
7
From page :
769
To page :
775
Abstract :
Polyvinyl alcohol [PVA]–iodine complex doped mesoporous TiO2 (PIT) and iodine doped (IT) catalysts were prepared by hydrothermal method, using tetrabutyl titanate as precursor, potassium iodate and iodine as iodine sources. The as-prepared PIT and IT catalysts were characterized by UV–vis, XRD, FESEM, BET, TG/DTA, XPS and photoluminescence (PL) spectroscopy. Production of radical dotOH radicals on the surface of photocatalyst was detected by the PL technique using terephthalic acid as a probe molecule. The influences of calcinated temperature on the structure and properties of the catalysts were investigated. The photocatalytic activity of catalysts was evaluated through photocatalytic decolorization of methylene blue (MB) aqueous solution. The results showed that PIT samples were anatase mesoporous TiO2 and their iodine content and mesoporous structure were influenced by calcinated temperature. Particle size of PIT samples was smaller than that of IT as a result of the PVA skeleton and regular structure. Because of the complexation of iodine and PVA, thermostability of iodine is improved and the amount of iodine in PIT calcinated at 200 °C (PIT-200) is higher than that of IT calcinated at same temperature. Light absorption range and intensity of PIT-200 has been greatly improved due to the synergy of iodine and carbon. The efficiency of photocatalysis for MB is greatly improved with TiO2 modified by PVA–I complex under simulated sun light irradiation.
Keywords :
TiO2 , PVA–iodine complex , Visible light , thermostability , Hydrothermal method
Journal title :
Applied Surface Science
Serial Year :
2013
Journal title :
Applied Surface Science
Record number :
1007028
Link To Document :
بازگشت