Recovering ammonia and potassium from wastewater is important for sustainable nutrient management and pollution mitigation. Membrane bioelectrochemical systems (MBESs) offer a promising approach for simultaneous recovery of ammonium (NH4+) and potassium (K+) from waste streams, although achieving distinct separation between these nutrient ions remains challenging. To address these limitations, this study aimed to improve reactor selectivity toward NH4+ and K+ to enhance nitrogen recovery while replacing the conventional oxygen reduction reaction with a solid-state electrode to reduce the aeration energy consumption. Here, we couple an ion-selective redox-active cathode based on Prussian blue analogues, potassium nickel hexacyanoferrate (KNiHCF), with a microbial fuel cell to evaluate ion intercalation behaviors and simultaneously recover NH4+ and K+ from synthetic wastewater. More electrons were produced to intercalate cations with the Na+-based catholyte than the Mg2+-based one. In most catholyte solutions, the electrode showed a preferential uptake of K+ and NH4+. The transport numbers indicated that the initial catholyte background cations (Na+ or Mg2+) played a critical role in facilitating transport of the target cations from the anolyte to the catholyte. When NH4+ was initially present in the catholyte, more than 60% of electrode occupancy corresponded to NH4+. These results demonstrate that catholyte composition strongly influences ion transport and selectivity in KNiHCF-coupled MBES systems.
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Tang et al. (2026) studied this question.
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