Experimental study demonstrates efficient phosphorus recovery from wastewater using electrochemically activated magnesite, indicating a reagent-saving treatment pathway.
Phosphorus recovery from wastewater can reduce dependence on phosphate rock and help control eutrophication. Struvite crystallization is a promising recovery route, but conventional processes often require soluble magnesium salts and alkaline reagents. This study used electrochemical activation of natural magnesite to supply Mg2+ in situ for magnesium ammonium phosphate (MAP) formation. Magnesite dissolution provided Mg2+, while cathodic water reduction generated a local alkaline zone that promoted phosphate precipitation. The effects of current density, N:P molar ratio, initial phosphorus concentration and initial pH were examined. XRD, SEM–EDS, and FTIR supported the formation of struvite-containing precipitates. Under the optimized conditions, namely an initial pH of 7.75, a nominal anodic current density of 28.21 A/m2, an initial phosphorus concentration of 6.41 mM, and an N:P molar ratio of 1.42:1, PO43−–P recovery, NH4+––N apparent removal and apparent MAP purity reached 57.56%, 52.26% and 62.56%, respectively. The apparent MAP purity represents an NH4+––N-based operational estimate rather than an absolute quantitative phase fraction. The decrease in aqueous NH4+––N should be regarded as apparent removal because NH3 volatilization or stripping may also occur near the alkaline cathode. This work provides a reagent-saving approach for phosphorus recovery by coupling Mg2+ release, cathodic alkalization and struvite crystallization.
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Wang et al. (2026) studied this question.
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