Mechanical activation of granulated copper slag (GCS) is carried out in the present study for the purposes of enhancing pozzolanic activity for the GCS. A vibration mill mills the GCS for 1, 2, and 3 h to produce samples with specific surface area of 0.67, 1.03 and 1.37 m²/g, respectively. The samples are used to replace 30% cement (PC) to get 3 PC-GCS binders. The hydration heat and compressive strength are measured for the binders and derivative thermogravimetric /thermogravimetric analysis (DTG/TGA), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM) are used to characterize the paste samples. It is shown that cumulative heat and compressive strength at different ages of hydration and curing, respectively, are higher for the binders blending the GCS milled for a longer time. The compressive strength after 90 d of curing for the binder with the longest milling time reaches 35.7 MPa, which is higher than the strength of other binders and close to the strength value of 39.3 MPa obtained by the PC pastes. The percentage of fixed lime by the binder pastes at 28 days is correlated with the degree of pozzolanic reaction and strength development. The percentage is higher for the binder blending the GCS with longer milling time and higher specific surface area. The pastes with binders blending the GCS of specific surface area of 0.67 and 1.37 m²/g fix lime of 15.20 and 21.15%, respectively. These results together with results from X-ray diffraction (XRD), FTIR, and SEM investigations demonstrate that the mechanical activation via vibratory milling is an effective method to enhance the pozzolanic activity and the extent for cement substitution by the GCS as a suitable supplementary cementitious material (SCM).

Due to increased copper production and the associated environmental consequences, copper production processes need to be improved, considering the impact of their byproducts, among others slag. This study investigated the leaching of individual constituents of iron silicate slag from a copper smelter. This was done by characterising granulated samples of its constituents – glass, matte, speiss – to determine their leaching contribution. It was observed that leaching in distilled and deionised water without pH regulation achieved various natural pH for the constituents. At natural pH, glass (Cu, Zn) and speiss (Ni, Sb) contributed to leaching. Static pH titrations showed the increased leaching of Zn, Cu, Ni, As, and Sb with decreasing pH. The results showed that, an iron silicate slag consisting of glass, matte and speiss, contributes to leaching as follows: matte – Cu and Ni, speiss – Cu, Ni, As, and Sb. Zn leaching is similar among the constituents.

Water-granulated CaO-modified iron-silicate slags have shown beneficial properties for cement applications. To further evaluate potential applications, the leaching properties must be understood. Therefore, this study aims to characterise and assess the metal leaching of iron-silicate slags (2.6% CaO) modified with lime (CaO, up to 20 wt.%) produced on both laboratory and industrial scales. The granulated samples showed amorphous contents for the studied CaO range. Generally, the metal content of the samples decreased with the increasing CaO content. Batch leaching tests were conducted on the slags, and the metal leaching and CaO content of the slag were strongly correlated. The leaching of Zn and Cu decreased with the increasing CaO content in the slag. Overall, the slags with 12–13% CaO exhibited minimal leaching of Zn, Cu, Ni, and Sb. These findings indicate that CaO influences the properties of the slag and can suppress metal leaching from water-granulated iron-silicate slags.

The zinc in the fayalite slag of copper smelters, in which Zn-containing raw materials are used, is mainly found to be in oxidic phases, such as glassy iron silicate. During the slag water granulation process, the molten slag is heated, whereby the granulated slag achieves varying granulation temperatures. Therefore, in this study, we aimed to characterize and assess the leaching behavior of a synthesized Fe-saturated (Fe_X,Zn_(1−X))₂SiO₄ system to understand the dependance of the zinc leaching behavior on the parameters of the ZnO content (1–10 wt.%) and granulation temperature (1300 or 1400 °C). It was found that the Zn leaching increased with the increasing Zn content and granulation temperature, using both batch and static pH leaching methods. Zn leaching was further increased at pH 5 using diluted nitric acid under oxidation conditions. Among the oxides in the samples—fayalite, spinel, and glass—glass was found to contribute to Zn leaching, owing to its weathering during pH-titration.

Granulated iron silicate slag, a by-product of pyrometallurgical copper extraction, has excellent properties for construction applications. Slag modification with CaO enhances the application properties regarding pozzolanic reactivity, potentially extending slag use in the future. The slags’ short-term leaching behavior has already been investigated with promising results, while the long-term leaching effects are less studied. Therefore, this study aims to determine the long-term leaching effects on CaO-modified iron silicate slags. The CaO-modifications were conducted during full-scale slag treatment operation. The slags were characterized and leached, and the remaining slags were investigated regarding the formation of secondary phases. The long-term leaching of main and trace elements was determined over 30 days using a dynamic leaching method corresponding to an extended time period. The leaching tests showed increased leaching of the main slag elements (Si, Ca). Zn and Cu showed peak leaching after four days of leaching, and the leaching of As and Sb decreased with the increasing CaO content in the samples. After dynamic leaching, secondary phases formed on the Cu-containing inclusions on the sample surfaces. Independent of the CaO content, the leaching of Cu was increased when subjected to external acidic and oxidating conditions using static pH titration at pH 5 in dilute nitric acid.