Synthesis of TiO2-based Nanomaterials and their Application in Arsenic Removal from Drinking Water

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Event details

Date 19.11.2008
Hour 14:15
Speaker Dr Deedar Nabi
Location
GR C1 564
Category Conferences - Seminars
Pure TiO (108 nm) and iron-doped TiO,Fe0.0063Ti0.9937O2, (65 nm) nanoparticles synthesized via sol-gel process were used along with General Purpose Reagent (GPR) TiO2 (325 nm) for studies of Arsenic removal from drinking water. These nanopatricles were in 100 % anatase crystalline phase. Energy dispersive elemental analysis indicated better percentage purity of lab synthesized nanoparticles as compared to GPR TiO. Yellow orange color of doped TiO22 showed a red shift in absorption wavelength from 387.5 nm to around 435 nm, thereby making the doped species visible light responsive. Pure TiO2 nanoparticles were successfully immobilized by generating titania-coated sand (TCS) singly (TCS-1) and doubly (TCS-2) via the sol-gel process. To see the effects of different conditions on Arsenic adsorption, five systems were used, viz., As(V) in Air-Light , As(III) in Air-Light, Air-Sunlight, Air-Dark and Nitrogen-Dark conditions. Kinetics of adsorption followed pseudo-second order rate law except for As(III)-Air-Light system which followed Elovich model. Adsorption of Arsenic on the adsorbents followed Freundlich and Langmuir model. Iron-doped TiO showed higher affinity for Arsenic than pure TiO22 which in turn showed greater affinity than GPR TiO2. Similarly, TCS-2 showed higher Arsenic affinity than TCS-1. Removal of As(III) was higher in light and oxidizing conditions than in dark and anoxic conditions. From pH dependence behavior, Point of Zero Charge of the nanoadsorbents was estimated to be around 7. Arsenic adsorption decreased with increase in pH. In TCS column test, 98% of As(V) and As(III) was removed with no leaching of TiO up to 1500 and 1450 bed volumes, respectively.

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