Article ID Journal Published Year Pages File Type
607789 Journal of Colloid and Interface Science 2013 9 Pages PDF
Abstract

Adsorption of fluoride from water onto titanium dioxide (TiO2) powder was investigated. The sorbent was crystalline TiO2 composed of mostly anatase with a specific surface area of 56 m2/g. Adsorption kinetics and isotherm experiments were performed using an aqueous solution with bicarbonate alkalinity representative of natural waters. Adsorption kinetics data showed that maximum adsorption of fluoride occurred within 3 h, following a pseudo-second order kinetics model. Adsorption isotherm data followed the Langmuir equation, indicating favorable adsorption of fluoride onto TiO2, while results from the Dubinin–Radushkevich model are indicative of physical adsorption of fluoride. Adsorption of fluoride increased with decreasing solution pH. Maximum adsorption of fluoride occurred within the pH range of 2–5, while approximately 75% of maximum adsorption was obtained in the pH range of 7–8 with rapidly declining adsorption above pH 9. The pHpzc data for TiO2 indicated the preferred adsorption of fluoride onto the acidic surface of TiO2. Higher bicarbonate concentrations in solution increased the solution pH which was conducive to a decrease in adsorption of fluoride onto the surface of TiO2 at higher pH. Overall, the solution pH was the main factor controlling the uptake of fluoride by TiO2.

Graphical abstractFigure optionsDownload full-size imageDownload high-quality image (261 K)Download as PowerPoint slideHighlights► The solution pH was the main factor controlling the adsorption of fluoride onto TiO2. ► A mechanism for the adsorption of fluoride onto crystalline TiO2 was proposed. ► The adsorption isotherm data indicate the favorable physisorption of fluoride. ► The distribution of active sites on the surface of TiO2 was heterogeneous. ► The adsorption of fluoride followed a pseudo-second order kinetics model.

Related Topics
Physical Sciences and Engineering Chemical Engineering Colloid and Surface Chemistry
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