Effectiveness and mechanism of aluminum/iron co-modified calcite capping and amendment for controlling phosphorus release from sediments

The effectiveness and mechanism of aluminum/iron co-modified calcite (Al/Fe-CA) for the control of phosphorus (P) liberation from sediments was investigated. The results showed that Al/Fe-CA possessed good sorption performance for phosphate, and the maximum phosphate sorption capacity for Al/Fe-CA could reach 27.0 mg/g. The major mechanisms involved the surface adsorption of phosphate on calcite, the precipitation between phosphate and Ca2+ leached from calcite, and the ligand exchange between Al/Fe-bound hydroxyl groups and phosphate to form the Al-O-P and Fe-O-P inner-sphere complexes. The re-releasing risk of Al/Fe-CA-bound P under the circumstances of normal pH (5-9) and reducing environment was very low. Al/Fe-CA addition could significantly reduce the risk of P releasing from sediment to overlying water (OL-water), and the inactivation of mobile P, reactive soluble P (SRP) and diffusive gradient in thin-films (DGT)-labile P in sediment by Al/Fe-CA had a great part in the suppression of sediment-P liberation to OL-water by the Al/Fe-CA amendment. Al/FeCA capping and fabric-wrapped Al/Fe-CA capping both could greatly reduce the risk of P releasing from sediment into OL-water, and the formation of a static layer with low concentrations of SRP and DGT-labile P in the upper sediment was the key to sustaining a high P controlling efficiency. When the applied mode of Al/Fe-CA varied from capping to amendment, although the inactivation efficiency of DGT-labile P in the overlying water and upper sediment by Al/Fe-CA would decrease to a certain degree, the inactivation efficiency of DGTlabile P in the lower sediment by Al/Fe-CA would increase. Results of this study suggest that Al/Fe-CA has the high potential to be used as an active capping or amendment material for the management of internal P loading in surface water bodies.