Multi-metal contaminant mobilizations by natural colloids and nanoparticles in paddy soils during reduction and reoxidation

J Hazard Mater. 2024 Jan 5:461:132684. doi: 10.1016/j.jhazmat.2023.132684. Epub 2023 Oct 4.

Abstract

Naturally-occurring colloids and nanoparticles are crucial in transporting heavy metal contaminants in soil-water systems. However, information on particle-bound metals' size distribution and elemental composition in paddy soils under redox-fluctuation is scarce. Here, we investigated the mobilization of Cu, Cd, and Pb-containing nanoparticles and colloids in four contaminated soils with distinctive geochemical properties during reduction and subsequent re-oxidation. Using AF4-UV-ICP-MS and STEM-EDS, we observed that particle-bound metals were primarily associated with two sizes ranges: 0.3-40 kDa (F1) and 130 kDa-450 nm (F2), which mainly consisted of organic matter (OM), iron hydroxide and clay minerals. Cu and Pb were more likely bound to colloid than Cd. Colloidal Cu, Pb and Cd accounted for averages of 83.2%, 72.4% and 19.8% of their total concentration in solution (<0.45 µm) during soil reduction, and decreased during soil re-oxidation. This proportion was also positively correlated with aqueous pH and DOC but negatively correlated with Eh. Further quantitative analysis demonstrated that Cu/Cd positively correlated with OM at nanometric scale (F1). This study provides quantitative insights into the size, composition and abundance of polymetallic pollutant-carrying particles in paddy soils during redox fluctuation, and highlights the importance of nanometric interactions between OM and toxic cationic metals for their release.

Keywords: Colloids; Field-flow fractionation; Heavy metals; Nanoparticle; Redox.