Fluoride in drinking water above permissible levels is responsible for dental and skeletal fluorosis. In this study, removal of fluoride ions from water using phosphoric acid treated lime was investigated in continuous and point-of-use system operations. In the continuous column operations, fluoride removal performance was investigated as a function of the fluoride concentration, flow rate and amount of adsorbent mass. Early saturation and lower fluoride removal were observed at higher flow rate and initial concentration, and at lower mass. Two domestic defluoridation point-of-use systems operated intermittently to process 20 ℓ•day −1 of water were used. High fluoride uptake capacity (FUC) from groundwater was observed depicting the suitability of the new media in defluoridation. However, further research is required to optimise the point-ofuse systems performances.
Fluoride in drinking water above permissible levels is responsible for human dental and skeletal fluorosis. Adsorptive based defluoridation is the most popular technique with several end-user applications. Consequently, this paper describes the fluoride removal potential of a novel sorbent, limestone-derived apatite from drinking water. The adsorbent was prepared by calcining limestone followed by reacting with orthophosphoric acid. Batch sorption studies were performed as a function of contact time, pH, initial fluoride concentration, temperature and adsorbent dose. Sorption of fluoride was found to be pH dependent with a maximum occurring in the pH range of 5-9. The authors also observed that the material had a buffering effect on the same pH range. Meanwhile, the adsorption capacity was found to increase with temperature, depicting the endothermic nature of the adsorption process and decreases with adsorbent mass. The equilibrium data was well described by the conventional Langmuir isotherm, from which isotherm the maximum adsorption capacity was determined as 22.2 mg/g. From the kinetic perspective, the fluoride adsorptive reaction followed the pseudo-second order mechanism.
Fluoride in drinking water above permissible levels is responsible for human dental and skeletal fluorosis. Adsorptive based defluoridation is the most popular technique with several end-user applications. Consequently, this paper describes the fluoride removal potential of a novel sorbent, limestone-derived apatite from drinking water. The adsorbent was prepared by calcining limestone followed by reacting with orthophosphoric acid. Batch sorption studies were performed as a function of contact time, pH, initial fluoride concentration, temperature and adsorbent dose. Sorption of fluoride was found to be pH dependent with a maximum occurring in the pH range of 5-9. The authors also observed that the material had a buffering effect on the same pH range. Meanwhile, the adsorption capacity was found to increase with temperature, depicting the endothermic nature of the adsorption process and decreases with adsorbent mass. The equilibrium data was well described by the conventional Langmuir isotherm, from which isotherm the maximum adsorption capacity was determined as 22.2 mg/g. From the kinetic perspective, the fluoride adsorptive reaction followed the pseudo-second order mechanism.
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