TiO 2 porous ceramic/Ag–AgCl composite was prepared by incorporating AgCl nanoparticles within the bulk of TiO 2 porous ceramic followed by reducing Ag + in the AgCl particles to Ag 0 species under visible light irradiation. The porous TiO 2 ceramic was physically robust and chemically durable, and the porous structure facilitated the implantation of AgCl NPs. Compared with the bare TiO 2 ceramic, TiO 2 porous ceramic/Ag–AgCl composite exhibited higher photocatalytic performance for the degradation of MO and RhB under visible light irradiation. The reaction rate constants k of MO and RhB degradation over TiO 2 porous ceramic/Ag–AgCl composite was respectively 6.25 times and 3.62 times higher than those recorded over the bare TiO 2 porous ceramic. The photocatalytic activity showed virtually no decline after four times cyclic experiments under visible light irradiation. Scanning electron microscopy, energy dispersive X-ray analysis, X-ray diffraction, UV–Vis diffuse reflectance spectroscopy, photoluminescence spectra and X-ray photoelectron spectroscopy were used to characterize the TiO 2 porous ceramic/Ag–AgCl composite.
Su Huanhuan,Lv Xiang,Zhang Zhengyi,Yu Jiajie,Wang Tianhe
Fe 2 O 3 –TiO 2 porous ceramic (Fe/TiPC) beads with photo-catalytic performances and high adsorption capacities were prepared by a simple high temperature solid reaction and were applied for arsenic removal from drinking water. The microstructure and morphology of Fe/TiPC were characterized by X-ray diffraction and scanning electron microscopy. More than 90% removal ratio for As (III) and As (V) were respectively achieved by Fe/TiPC within 2 h under UV irradiation. The Langmuir capacity values of Fe/TiPC for As (III) and As (V) were 13.86 and 15.73 mg/g, respectively. In addition, Fe/TiPC could be reused for up to five times without significant reduction in the photocatalytic sensitivity and adsorption capacity aspects. Good catalytic oxidation performances and high adsorption capacities as well as a sample preparation for Fe/TiPC suggest that the composites may have practical prospects for the As (III) and As (V) removal from contaminated water.