Purpose
This work deals with the application of a solidification/stabilization process with the aim to obtain safe and reusable granular materials from a polluted soil and to elucidate the mechanisms involved in the retention of several heavy metals.
Materials and methods
The High Performance Solidification/Stabilization (HPSS®) process was applied to the selected contaminated soil by using both ordinary Portland cement and calcium aluminate cement, as well as several binders prepared by combining these two types of cement in different proportions. Leaching and mechanical tests were carried out to evaluate the performances of the proposed binders in the pellets produced by the HPSS® process, while XRD analysis and SEM/EDX imaging were used to investigate the phase composition and internal microstructure of the treated samples.
Result and discussion
The examination of the obtained granular materials revealed that the immobilization of Sb was mainly related to its inclusion within calcium silicate hydrates’ structure; the immobilization of Cr, Pb, Ni, Co, Zn and Tl was associated with the eluate pH and their incorporation within ettringite structure, while for Se, Cu, Ba and V, the main retention mechanism was physical encapsulation. In addition, the application of a wet conditioning process improved the materials’ performance, leading to granules always satisfying the Italian regulatory requirements for reuse.
Conclusions
The findings obtained in this study were useful to better elucidate the mechanisms involved in the retention of heavy metals by several binders, contributing to the development of sustainable management strategies for contaminated soils and sediments through their transformation into reusable materials.
Graphical abstract
Degraded land requires rapid and suitable remedial actions, thus appropriate and fast methodological approaches for estimating the spatial distribution of contaminants are needed. In this context, a methodological approach combining isotopic measurements, heavy metals concentrations mapping, X‐ray diffraction, and cluster analysis, was applied to characterize a polluted industrial site where the contamination due to improper waste disposal could have spread also into the surrounding fields. This approach was applied to a set of representative topsoil (from 15 to 30 cm depth) and subsoil (from 130 to 150 cm depth) samples, selected either inside or outside the contaminated site. The X‐ray diffraction analysis highlighted that only the mineralogy of the subsoil below the buried waste was noticeably altered, while the concentration mapping highlighted that the levels of several heavy metals on the edge of the contaminated site, at both depths, were very similar to those found in the samples from the outside. Based on these findings, Pb was used as a tracer for heavy metal pollution by its stable isotopes' analysis. The cluster analysis of the isotopic measurements revealed that only the contamination detected inside the industrial site could be attributed to the pollutants migration from the buried waste. Conversely, the contaminants concentrations found in the topsoil samples taken outside the site could be ascribed to contamination sources other than the polluted waste present inside the site.
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