Structural transformation investigations of δ to α manganese dioxides: Phosphate sorption and its mechanism

Abstract

The elevation of environmental phosphate levels can negatively impact both the natural environment and human health. To address this issue, a series of MnO2 sorbents were investigated in this study. A facile one-pot synthesis method was employed to fabricate distinct morphologies and crystalline structures by controlling the hydrothermal duration. As the hydrothermal duration was prolonged, the samples demonstrated a pronounced enhancement of stability and crystalline phases, along with a corresponding increase in structural oxygen vacancies. A series of sorption performance tests were conducted, including pH effect, sorption isotherm, sorption kinetics, co-existing ions and sorption–desorption cycles experiments. It was revealed that manganese dissolution, the surface charge of the sorbents, and the phosphate species at different pH values collectively influenced the sorption process. The sorbent α-MnO2-120 h, with the highest oxygen vacancy ratio, exhibited the best sorption performance towards phosphate ions, with the maximum sorption capacity at pH 7. The highest removal rate and kd value were 82.63 % and 2.29 × 103 mL g−1, respectively, at the initial concentration of 30.7 mg PO4 g−1. The α-MnO2-120 h sorbent exhibited excellent selectivity in the presence of NO3−, SO42−, CO32−, and SiO32−. Furthermore, the regenerated material exhibited only a 6 % decrease in phosphate removal efficiency after five cycles, with no structural changes observed. A novel mechanism was proposed, highlighting the dominance of covalent chemical reactions in the sorption process. In particular, the participation of oxygen vacancies in sorbents contributed to enhancing the effective removal of phosphate ions. Overall, this study successfully demonstrated that synthesized α-MnO2 is a promising sorbent for phosphate removal.