Behavior of iron and other heavy metals in passivated sediments and the coupling effect on phosphorus

In situ passivation, which is easy to operate and affordable, is one of the most commonly used methods for sediment phosphorus (P) remediation. Understanding the behavior of iron and other heavy metals in passivated sediments is important for alleviating lake eutrophication and for ensuring drinking water safety. In this study, we investigated the behavior of P, Fe, Mn, Cd, Co, and Pb in lanthanum modified bentonite (LMB, Phoslock®) and polyaluminum chloride (PAC)-passivated sediments using intact sediment cores. Rhizon sampler and diffusive gradients in thin films technology (DGT) were respectively used to collect soluble and labile substances in sediment; a modified sequential selective extraction method was used to characterize metal forms. Results showed that LMB reduced soluble reactive phosphorus (SRP) at sediment depths of 0 ~ -15 mm and DGT-labile P flux at 0 ~ -50 mm. Correlation between DGT-labile P and Fe (R² = 0.71) indicated that P mobility in the LMB group was affected by the behavior of Fe. PAC decreased SRP at sediment depths of 0, -5, -10, -15, -20, -25, and -50 mm with removal rates of 100%, 90%, 45%, 35%, 81%, 89%, and 100%, respectively. DGT-labile P flux was decreased by PAC at 0 ~ -10 mm and -50 ~ -110 mm, but increased at -10 ~ -50 mm; this is a result of synthetical effect by Al flocs adsorption and Fe(III) reductive dissolution. LMB decreased Cd, Co, and Pb in LMB layer in carbonate, reducible, and oxidizable forms. PAC decreased Cd mobility but caused the transformation of Co and Pb from reducible to other forms because of Fe(III) reductive dissolution. Those results indicate that sedimentary Fe plays an important role in in situ passivation. We suggest modifying passivators to Fe(II) adsorbents and increasing DO permeability of sediment to promote the formation of an Fe(III) passivation layer and hence the effectiveness of P control.