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A column experiment at a laboratory level was carried out to assess the effect of the application of nanotechnology in the decontamination of soils and alluvial deposits with high levels of potentially toxic elements (PTEs). A suspension of zero-valent iron nanoparticles (nZVI) was injected at three different concentrations in selected samples (two sediments, one soil). For most of the elements, the retention by nZVI was proportional to the concentration of the suspension and the trend was similar. Metals were immobilized by adsorption on the surface layer of the nanoparticles and/or by complexation, co-precipitation, and chemical reduction. By day 60 following injection, the nZVI lost reactivity and the retained species were desorbed and back into the soluble phase. The definition of spatial patterns for PTEs’ distribution allowed for the construction of contamination risk maps using a geostatistical simulation approach. The analysis obtained from the extractable contents of five target elements (Zn, Cu, Cd, Pb, As) was cross-checked with the estimated map network to assess their retention efficiency. Data from the analysis of these elements, in the extractable phase and in the porewater of the sediments/soils, indicate the nZVI injection as a suitable technique for reducing the risk level of PTEs in contaminated Fe-rich tropical environments.
In areas contaminated by potentially toxic elements (PTEs), knowledge of processes of metal mobilisation is the basis for the choice of appropriate remediation methodologies. The mobilisation of metals is a function of several factors, and the response to these factors must be well known during the planning of remediation strategies. The activity of an ore metallurgical plant in South‐East Brazil resulted in major contamination by several heavy metals. Reversing the contamination’s negative impact required geochemical assessment of the area, including the physicochemical characterisation, quantification, and delimitation of PTEs, and the rating of the solubilisation/mobilisation capacity of these elements. The definition of spatial patterns for PTEs’ distribution allowed the construction of contamination risk maps which work as a tool for the mitigation and control of the contamination plume. The chemical analysis of interstitial water and selective and sequential extraction methodologies showed that elements that occur in the environment in critical concentrations (Zn, Cd, Pb, As) are mostly associated with easily mobilised forms (soluble, exchangeable cations, associated with Mn oxides). Given the great mobility of the contamination plume, any process of removal of contaminated material becomes unfeasible, thus the strategy of remediation for the stream and associated alluvial deposits must be based on methods of in situ decontamination.