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    Microbial disinfection of water with endotoxin degradation by photocatalysis using Ag@TiO2 core shell nanoparticles
    (Springer Verlag service@springer.de, 2016) Sreeja, S.; Shetty K, K.V.
    The studies on photocatalytic disinfection of water contaminated with Escherichia coli using Ag core and TiO2 shell (Ag@TiO2) nanoparticles under UV irradiation showed that these nanoparticles are very efficient in water disinfection both in their free and immobilised form. Complete disinfection of 40 × 108 CFU/mL could be achieved in 60 min with 0.4 g/L catalyst loading and in 35 min with 1 g/L catalyst loading. Ag@TiO2 nanoparticles were found to be superior to TiO2 nanoparticles in photocatalytic disinfection of water. Kinetics of disinfection followed Chick’s law, and the pseudo-first-order rate constant was 0.0168 min?1 for a catalyst loading of 0.1 g/L. Disinfection of water and degradation of endotoxins (harmful disinfection residual) occurred simultaneously during photocatalysis thereby making the treated water safe for use. Endotoxin degradation showed a shifting order of kinetics. The rate of photocatalysis with nanoparticles immobilised in cellulose acetate film was marginally lower as compared to that of free nanoparticles. Negligible Ag ion leakage and re-growth of cells post-photo-catalytic treatment of water confirmed that complete disintegration of E. coli occurred during photocatalysis making the treated water safe for use. Therefore, Ag@TiO2 nanoparticles have a potential for large-scale application in drinking water treatment plants and household purification units. © 2016, Springer-Verlag Berlin Heidelberg.
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    Photocatalytic water disinfection under solar irradiation by Ag@TiO2 core-shell structured nanoparticles
    (Elsevier Ltd, 2017) Sreeja, S.; Shetty K, V.K.
    The Ag core-TiO2 shell structured (Ag@TiO2) nanoparticles were found to be efficient in the disinfection of water under solar light irradiation both in free and immobilized form. Complete disinfection of 40 ? 108 CFU/mL Escherchia coli cells was achieved in 15 min by solar photocatalysis with 0.4 g/L Ag@TiO2 catalyst loading. Ag@TiO2 nanoparticles were found to be superior to TiO2 nanoparticles in solar disinfection. Photocatalysis rate was found to increase with increase in catalyst loading and with decrease in cell concentration. Ag@TiO2 nanoparticles showed their efficacy in the degradation of endotoxin, a harmful disinfection byproduct. Kinetics of solar disinfection with Ag@TiO2 nanoparticles followed Chick's law. The kinetics of endotoxin degradation followed zero order kinetics at high concentrations of endotoxin. However at lower concentrations, rate followed a nth order model with n = 6.99. A lower rate of photocatalytic disinfection with Ag@TiO2 nanoparticles immobilized on cellulose acetate as compared to that in their free form was observed, owing to diffusional and light penetration limitations. The re-growth of cells after photocatalytic disinfection was below the detectable limits, thus proving the potential of the process to produce safe drinking water. Ag@TiO2 nanoparticles can find potential application in solar water disinfection and the process which harnesses the solar energy may prove to be energy efficient and economical, thus can be easily adopted for large scale applications and portable drinking water treatment units for domestic applications. © 2017 Elsevier Ltd