Abstract
Selective precipitation of phosphate from fluoride-containing wastewater was studied using magnesium salts. Wastewater sampled from a semiconductor manufacture was found to contain 936 mg/L of fluoride (F−), 640 mg/L of sulfate (SO42−), 118 mg/L of phosphate (PO43−), and 26.72 mg/L ammonium (NH4+). Magnesium chloride (MgCl2) was more effective than magnesium oxide (MgO) in inducing precipitation reactions between magnesium and phosphate. Effects of both molar ratio ([Mg2+]:[PO43−]) and pH were examined and experimental results were compared with those from equilibrium modeling by PHREEQC. A total of 41.72% of phosphate was removed and recovered when at molar ratio of 3:2 and pH of 10. Precipitation of phosphate increased with increasing molar ratio and 66.19% of phosphate was recovered when molar ratio was 3:1. Precipitation of phosphate increased as pH changed from 8 to 10. However, it decreased as pH increased from 10 to 12, probably because of competition between phosphate and hydroxyl (OH−) ions. Solid precipitates were characterized by field emission scanning electron microscope with energy dispersive spectrometer and X-ray diffraction. In accordance with theoretical modeling, it was found that the precipitate in pH range of 8–10 was predominantly bobierrite [Mg3(PO4)2.8H2O] and some amorphous precipitates. However, brucite [Mg(OH)2] precipitate would start to form when pH became higher than 10. Results showed that MgCl2 can be a selective precipitation reagent for phosphate removal from semiconductor wastewater since it does not form precipitate with fluoride, sulfate, and ammonium.
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