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In order to realize the ideal water treatment in a green and energy saving manner, TiO 2 based multifunctional membrane proved to be a promising approach owing to its capability in utilizing visible light for photocatalytic pollutant degradation and disinfection of bacteria. However, few studies were found about the investigation of antibacterial abilities arising from the intrinsic properties of membrane and its minor composition. Here, a multifunctional membrane was created via a green approach to integrate the merits of hierarchical Ag/AgBr/TNF composites with micro-/-nano porous structures, the intrinsic antibacterial abilities of Ag, and the visible light absorption capability of AgBr. The synergy effects made it being a promising multifunctional membrane for concurrent water filtration and disinfection in a sustainable way. Through a versatile characterization techniques of FESEM, XRD, TES, XPS, and UV-vis spectrometer, the morphology, structure and surface properties of the well prepared Ag/AgBr/TNF multifunctional membrane was thoroughly studied to reveal the deep mechanism behind the high flux, high photocatalytic degradation and disinfection efficiency under visible light. It indicates that the Ag/AgBr/TNF multifunctional membrane exhibited better photocatalytic activity, higher water permeate flux, and higher disinfection abilities over commercial P25 membrane under visible light. Besides the deep mechanism elaborated, the key factors in terms of predominant oxidative species was also exploited in details. This further solidify the broad future of the developed multifunctional membrane. In view of the roaring demand of advanced water treatment and disinfection technology, it is reasonable to believe our developed visible light responsive Ag/AgBr/TNF multifunctional membrane will show great significances to a green and clean future. [ABSTRACT FROM AUTHOR]

Abstract: Here, hierarchically meso/nanoporous TiO2 was successfully fabricated by a facile and efficient hydrolysis and calcination method using Ti(OC4H9)4 and K2S2O8 as precursors. The hydrosol was firstly prepared by drop-wise adding ethanol dissolved Ti(OC4H9)4 solution into acetone dissolved K2S2O8 solution under a vigorous stirring and heating condition. After being sufficiently hydrolyzed, the hydrosol was calcined to promote the crystallization of TiO2 and successfully dope S and C on TiO2. The calcination temperature significantly affects the doping of S and C on TiO2, crystallization of TiO2, formation of hierarchically meso/nanoporous structure of TiO2 and its light absorption capability. The S- and C-codoped TiO2 exhibits high photocatalytic H2 generation efficiency in a water/methanol sacrificial reagent system under the irradiation of UV light. The high photocatalytic efficiency is dependent on the comprehensively competing effects of the codoping of S and C, crystallization, specific surface area and light absorption capability. The S- and C-codoped TiO2 calcined at 600°C demonstrates the highest photocatalytic H2 generation efficiency, which is ascribed to the balanced synergy of the abovementioned factors. [Copyright &y& Elsevier]

Abstract: Hierarchical porous TiO2 hollow microspheres were synthesized by a facile approach from a one-step template method. This novel approach avoids tedious multiple steps from conventional template method for fabricating hierarchical porous and hollow microspheres. The as-prepared microspheres were characterized by XRD, SEM, TEM, nitrogen adsorption, and UV–vis DRS. Its photocatalytic activity was demonstrated in the photocatalytic degradation of Rhodamine B. Structural characterization indicates that the as-prepared microspheres had a hollow interior and a hierarchical porous structure with both large and small mesopores on its surface. The average diameters and BET surface areas of the hierarchical porous TiO2 hollow microspheres were 1.5μm and 117m2/g, respectively. Optical adsorption investigation shows that the hierarchical porous TiO2 hollow microspheres possessed the optical band gap of 3.42eV. A possible formation mechanism for the hierarchical porous TiO2 hollow microspheres was discussed. The hierarchical porous TiO2 hollow microspheres exhibited much higher photocatalytic activity than the commercial P25 TiO2. In addition, the as-prepared microspheres can be easily recycling for reuse. All these advantages show a bright future for this microspheric photocatalyst in environmental purification. [Copyright &y& Elsevier]

Abstract: Here we present a simple two-phase assembling method to produce high-quality graphene oxide–TiO2 nanorod composites (GO–TiO2 NRCs) on gram scale. TiO2 nanorods dispersed in toluene are synthesized from a facile two-phase hydrothermal method. The effective attachment of TiO2 nanorods on the whole GO sheets at the water–toluene interface is confirmed by Transmission Electron Microscope (TEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). The as-synthesized TiO2 nanorods show a slightly higher efficiency in the photocatalytic degradation of C. I. Acid Orange 7 (AO 7) irradiated under UV light (λ =254nm) and higher antibacterial activity under simulated sunlight than that of TiO2 nanoparticles with the same diameter. After combined with graphene oxide (GO), the GO–TiO2 NRCs show much higher photocatalytic activities than that of TiO2 nanorods alone and the GO–TiO2 nanoparticle composites (GO–TiO2 NPCs). The ratio of TiO2 and GO has no evident effect on the photocatalytic activity of GO–TiO2 NRCs when all the TiO2 nanorods are anchored on the GO sheets. The higher photocatalytic activity of GO–TiO2 NRCs is ascribed to the anti-charge recombination and the more (101) facets. Considering the superior photocatalytic activity of GO–TiO2 NRCs and the fact that they can been easily mass-produced, we expect this material may find important applications in environmental engineering and other fields. [Copyright &y& Elsevier]