Abstract
In the present study, alkaline hydrothermally treated titania nanoparticles (TiO2-HT) are prepared and followed by calcination at different low temperatures to improve TiO2 activity under visible light. The prepared photocatalysts (PCs) are characterized by different tools. TiO2-HT is scrutinized for decontamination of para-nitrophenol (PNP) and hexavalent chromium ions (Cr6+ ions) under simulated sunlight. TiO2-HT-300 and TiO2-HT-400 PCs have nanosized particle with large surface area of 148 and 116.26 m(2)/g, respectively. Additionally, XRD and FTIR proved formation of nanocrystalline anatase TiO2. The different calcined TiO2-HT materials show lower adsorption capacity for PNP and Cr6+ ions. TiO2-HT-300 and HT-TiO2-400 PCs have higher reduction rate of PNP than that of uncalcined temperature titania (HT-TiO2-U) powder. Complete conversion of PNP is achieved at natural pH after 180 min over TiO2-HT-300. As well, TiO2-HT-300 exhibits a superior photocatalytic removal of Cr6+ ions. The enhanced photocatalytic efficacy is ascribed to the synergism between higher surface area and particle size (quantum effect) of TiO2-HT-300. As results, HO center dot radicals are the main key active species for the photocatalytic degradation of PNP over TiO2-HT-300 PC but contribution of O-2(-) and h(+) holes is minor. The used method for preparation of TiO2-HT-300 reduces the cost preparation as well as environmental impact reduction. Finally, low temperature-calcined TiO2 is promising visible light active and an efficient photocatalyst with lower environmental impact for detoxification of PNP and Cr6+ ions from water.