fast-red-s and titanium-dioxide

A novel, simple, less time-consuming and cost-effective wet chemical technique was used to synthesis TiO2 nanoparticles and TiO2-SiO2 nanocomposites using Titanium tetra isopropoxide (TTIP) as a precursor relatively at low temperature in acidic pH. Titania sol was prepared by hydrolysis of TTIP and was mixed with silicic acid and tetrahydrofuran mixture. The reaction was carried out under vigorous stirring for 6h and dried at room temperature. The resulting powders were characterized by UV-Visible spectroscopy, Fourier transform infrared (FT-IR), X-ray diffraction, scanning electron microscope (SEM) and transmission electron microscope (TEM). The grain size of the particles was calculated by X-ray diffraction, surface morphology and chemical composition was determined from scanning electron microscopy-energy dispersive spectroscopy, metal oxide stretching was confirmed from FT-IR spectroscopy, band gap was calculated using UV-Visible spectroscopy. Surface area of the composite as calculated by BET analyzer and it was found to be 65 and 75 m(2)/g for TiO2 and TiO2-SiO2 respectively. The photocatalytic experiments were performed with aqueous solution of acid red 88 with TiO2 and TiO2-SiO2 batch studies for 4h irradiation, direct photolysis of TiO2 and TiO2-SiO2 contributed 94.2% and 96.5% decomposition in solar radiation for the optimized concentration of acid red 88.

Topics: Azo Compounds; Nanocomposites; Photochemical Processes; Silicon Dioxide; Spectrophotometry; Titanium

This paper reports an investigation into the effect of a number of operating factors on the removal of Acid Red 88 from an aqueous solution through photoelectrocatalysis: photocatalyst dose, dye concentration, pH, bias potential, and electrolyte concentration. The photocatalyst was Ni-TiO2 applied in suspension to the solution to achieve a larger catalyst surface area. The optimum values for photocatalyst dose, dye concentration, and electrolyte concentration turned out to be 0.6 mg L(-1), 50 mg L(-1), and 5 mg L(-1), respectively. Also, the best pH was found to be 7, and bias potential proved to be best at 1.6 V. The aqueous solution was characterized for its COD and TOC. Photocatalyst efficiency was evaluated using SEM and XRD techniques. The characterization of the post-treatment product using FT-IR, HPLC, and GC-MS studies revealed intermediate compounds. A pathway was proposed for the degradation of the dye. The energy required by the experiment was supplied by solar cells, meaning the money that would have otherwise been spent on electricity was saved. Cost analysis was also done for the treatment process.

Topics: Azo Compounds; Chromatography, High Pressure Liquid; Costs and Cost Analysis; Gas Chromatography-Mass Spectrometry; Hydrogen-Ion Concentration; Microscopy, Electron, Scanning; Nickel; Photolysis; Sodium Chloride; Spectrophotometry, Ultraviolet; Spectroscopy, Fourier Transform Infrared; Titanium; Water Pollutants, Chemical; X-Ray Diffraction