Evolution of geochemical and mineralogical parameters during in situ remediation of a marine shore tailings deposit by the implementation of a wetland cover

Abstract

We present data of the time-evolution of a remediation approach on a marine shore tailings deposit by the implementation of an artificial wetland. Two remediation cells were constructed: one in the northern area at sea-level and one in the central delta area (above sea-level) of the tailings. At the beginning, the “sea-level” remediation cell had a low pH (3.1), with high concentrations of dissolved metals and sulfate and chloride ions and showed sandy grain size. After wetland implementation, the “sea-level” remediation cell was rapidly water-saturated, the acidity was consumed, and after four months the efficiency of metal removal from solution was up to 79.5%–99.4% for Fe, 94.6%–99.9% for Mn, and 96.1%–99.6% for Zn. Al and Cu concentrations decreased below detection limit. The “above sea-level” remediation cell was characterized by the same pH (3.1) and finer grain size (clayey–silty), and with some lower element concentrations than in the “sea-level” cell. Even after one year of flooding, the “above sea-level” cell was not completely flooded, showing on-going sulfide oxidation in between the wetland cover and the groundwater level; the pH increased only to 4.4 and metal concentrations decreased only by 96% for Fe, 88% for Al, 51% for Cu, 97% for Mn, and 95% for Zn. During a dry period, the water level dropped in the “sea-level” cell, resulting in a seawater ingression, which triggered the desorption of As into solution. These data show that the applied remediation approach for this tailings deposit is successful, if the system is maintained water-saturated. Metal removal from solution was possible in both systems: first, as a result of sorption on Fe(III) hydroxide/and/or clay minerals and/or co-precipitation processes after rise of pH; and then, with more reducing conditions, due to metal sulfides precipitation.