Mobilization of colloids during sediment resuspension and its effect on the release of heavy metals and dissolved organic matter

Abstract

Natural colloids are important in mobilizing pollutants in aquatic environments. This study investigated the mobilization and aggregation of natural colloids during the sediment resuspension and re-sedimentation processes using nanoparticle tracking analysis. The metals and organic matter in overlying water were divided and examined in dissolved (<0.45 μm), colloidal (3 kDa – 0.45 μm), and truly dissolved (<3 kDa) forms. Excitation emission matrix−parallel factor analysis (EEM-PARAFAC) was used to characterize the dissolved organic matter (DOM). In overlying water, most natural colloids were < 200 nm before resuspension. An evident mobilization of colloids and an increase in colloid size were observed during resuspension. The formation of particles (>0.45 μm) and decreases of small colloids (<200 nm) indicated that resuspension promoted the aggregation of colloids. Mobilization of colloids was accompanied by increases in concentrations of Fe, Al, and organic carbon in colloidal fractions, which could be related to the formation of mineral-organic complexes under an oxic environment. The release of DOM from sediments mainly contributed to the truly dissolved humic-like fraction, and colloidal organic carbon accounted for, on average, 20 % of the total dissolved organic carbon (DOC). Fe and Al had the highest colloidal proportions as they are major compositions of inorganic colloids. Substantial removal of dissolved Al, Fe, Pb, and Zn occurred when colloids aggregated in the overlying water. Although the adsorption of suspended particles may also decrease the concentrations of dissolved metals, the increased proportions of colloidal metals indicated a possible role of colloids in this process. These findings provide insight into the behavior of colloids during the resuspension process and indicate that the aggregation of colloids could promote the removal of dissolved matter.