Conventional groundwater treatment plants consist of aeration and rapid sand filtration steps, that are merely designed and optimized for iron (Fe), manganese (Mn) and ammonium (NH4+) removal. Understanding the various reduction-oxidation pathways, and interactions of manganese and iron, can play a major role in optimizing the performance of such filters. Interestingly, it is found that under certain conditions, mobilization of dissolved manganese can occur in such filters, which can be critical to the filter operation. Therefore, the main aim of this research is to dive deep into studying the possibilities of manganese reduction pathways occurring at the top layer of the filter media of a groundwater filter. Secondly, the research also focuses on knowing how the removal of manganese is related to the oxidation by MnO2+O2 systems, and also how these systems interact with each other under different pH conditions.
To do so, manganese dioxide (MnO2) coated sand grains were obtained from the second filtration unit of Vitens groundwater treatment plant situated in Holten. Various batch scale experiments were done under aerobic as well as anoxic conditions, in the presence of Mn(II) or Fe(II). Additionally, the influence of pH on manganese removal efficiencies as well as the rates of both manganese and iron oxidation was investigated.
It was found that the dissolved Mn was a reduction product of MnO2-Fe(II) system, where Mn(IV) got reduced to Mn(II), reaching an Fe(II) : Mn(II) molar ratio of 3.65:1 instead of 2:1, as there was a significant difference between the calculated theoretical values and the measured experimental values of both Mn(II) and Fe(II). There was mobilization of Mn(II) which took place from the MnO2 surface, when there was a presence of Fe(II) in the system, which simultaneously got partially oxidized to Fe(III). Also, it was observed that manganese could be removed by MnO2 under anoxic conditions, although under aerobic conditions the removal efficiency was high (93.32% vs 71.83%). Apart from oxidation, there is a possibility of adsorption over MnO2 due to its high sorption capacity towards cations like Mn2+, Mn3+ and Fe2+. This research also showed that a small fraction of Mn(II) reacts with Mn(IV) to form Mn(III) as a reaction product, enhancing the mobilization of Mn(II).