Abstract
Elevated phosphorus and nitrogen concentrations in agricultural drainage are responsible for widespread declines in water quality across freshwater and marine receiving environments worldwide. Removal of P at source is particularly important because its tight biogeochemical cycling with iron (Fe), leads to preferential P−retention (over N) across the aquatic continuum, particularly in lake basins. This paper introduces new Fe−C−based composites (Fe(III)oxide/akaganite) designed for use in edge-of-field mitigations such as denitrifying bioreactors, with the goal of intercepting and retaining P on−farm. Our Fe−functionalised media had a net positive charge in the favourable range for P adsorption under the typical pH conditions encountered in denitrifying bioreactors (pH 5.5 − 6). Although functionalized wood (Fe-WC) had significantly higher P adsorption capacity than functionalised biochar (Fe-PyOM), 65.8 mg g-1 and 31.4 mg g-1, respectively; this was of comparable magnitude to powdered akaganite (107 mg g-1), despite large differences in particle size. Batch and column adsorption experiments indicate a multi−layer adsorption mechanism for P removal on Fe−PyOM and Fe−WC, which was further investigated using XPS, confirming dominant electrostatic P binding by Fe-functionalised media below pH 6, but an increasing importance of ligand exchange (Fe-O-P) at pH 8, particularly for Fe-PyOM. Based on the prevailing geochemistry of influent solutions to DBRs (pe ⁓ -8, pH ⁓ 6), we suggest that Fe−PyOM may be able to continuously adsorb P over a long timespans without requiring replenishment, due to its higher surface area, stability, and multiple P binding mechanisms.
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