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Highly photoactive bi-phase nanocrystalline TiO2 photocatalyst was prepared by a solvent evaporation-induced crystallization (SEIC) method, and calcined at different temperatures. The obtained TiO2 photocatalyst was characterized with X-ray diffraction (XRD), transmission electron microscopy (TEM) and BET surface areas. The photocatalytic activity was evaluated by the photocatalytic oxidation of acetone in air. The results show that solvent evaporation can promote the crystallization and phase transformation of TiO2 at 100℃. When calcination temperatures are below 600℃, the prepared TiO2 powders show bimodal pore size distributions in the mesoporous region. At 700℃, the pore size distributions exhibit monomodal distribution of the inter-aggregated pores due to the collapse of the intra-aggregated pores. At 100℃, the obtained TiO2 photocatalyst by this method shows good photocatalytic activity, and at 400℃, its photocatalytic activity exceeds that of Degussa P25. This may be attributed to the fact t
Highly photoactive bi-phase nanocrystalline TiO2 photocatalyst was prepared by a solvent evaporation-induced crystallization (SEIC) method, and calcined at different temperatures. The TiO2 photocatalyst was characterized with X-ray diffraction (XRD), transmission electron microscopy The photocatalytic activity was evaluated by the photocatalytic oxidation of acetone in air. The results show that the solvent evaporation can promote the crystallization and phase transformation of TiO2 at 100 ° C. When calcination temperatures are below 600 ° C., the prepared TiO2 powders show At 700 ° C, the pore size distributions exhibit monomodal distribution of the inter-aggregated pores due to the collapse of the intra-aggregated pores. At 100 ° C, the obtained TiO2 photocatalyst by this method shows good photocatalytic activity, and at 400 ° C, its photocatalytic activity exceeds that of Degussa P25. This may be a ttributed to the fact t