Some of the steel slag from ironworks and dredged soils from marine and waterfront engineering work are partially treated as waste. However, a mixture of these two kinds of waste has the potential to be used as construction materials when mixed, due to chemical reactions forming secondary phases. Utilizing waste of such kind as a resource will help to improve sustainability in society by reducing waste and replacing virgin resources such as cement. Recently, it was reported that mixtures of steel slag and dredged soil hardens under specific conditions. The phase compositions of dredged soils and steel slags vary depending on the quantity of each component, which results in unpredictable strength development of mixtures. The effect of the variations in the components of steel slags and dredged soils on strength development of the mixtures is not yet clear, limiting the utilization of both materials. Understanding the hardening mechanisms of the mixtures will enable the prediction of strength development. Focusing on the variations in the components in steel slags and, especially of dredged soils, this study aims to identify the components in both materials that affect the secondary phase formation that are responsible for strength development. We found support for suggestions that calcium silicate hydrate, C-S-H, is one of the secondary phases responsible for the strength development of the mixtures. From a comparison of two kinds of steel slags and various dredged soils, the amount of portlandite in the steel slags and the amount of amorphous silica in the dredged soils are suggested as a couple of the key components of starting materials involved in the C-S-H formation.

Indonesia is one of the largest Ni ore producers in the world and is also expected to be an important potential source of some critical metals (e.g., Co, Sc, rare‐earth elements, and platinum‐group elements). However, few studies have examined Ni laterite deposits in this country. In this study, we investigate Ni enrichment and the potential accumulation of critical metals in four laterite profiles with varying degrees of serpentinization and weathering intensity in the Soroako and Pomalaa mining areas of Sulawesi, Indonesia. We integrate geochemical evaluation with a mass‐balance approach and mineralogical analysis to better constrain the geochemical factors influencing the mobilization of Ni during lateritization. Nickel contents in the saprolite horizon of the profiles that are strongly weathered and developed over serpentinized peridotite are higher than those that are weakly weathered and developed over unserpentinized harzburgite. The bulk Ni contents of saprolite horizons are related to Ni contents of Ni‐bearing Mg‐phyllosilicates, which suggests that Ni remobilization is the main control on Ni enrichment in the profiles. Mass‐balance calculations reveal that the amounts of gained Fe and Ni in the profiles are positively correlated. This relationship indicates that the redistribution of Ni is likely controlled by the aging of Ni‐bearing goethite (dissolution/recrystallization) involving ligand‐promoted dissolution by organic matter and/or reductive dissolution by microbial activity near the surface. Critical metals show enrichment in specific horizons. Enrichments in Co and rare‐earth elements are strongly influenced by the formation of Mn‐oxyhydroxides in the oxide zone of the profiles. In contrast, Sc, Pt, and Pd show residual enrichment patterns, with grades influenced mainly by their initial contents in bedrock. The profiles show a positive correlation between Sc and Fe, as reported for other Ni laterite deposits. Among the critical metals, Sc, Pt, and Pd contents in the studied profiles are comparable with values reported from other Ni laterite deposits worldwide.

Carbonatites undergo various magmatic-hydrothermal processes during their evolution that are important for the enrichment of rare earth elements (REE). This geochemical, petrographic, and multi-isotope study on the Kangankunde carbonatite, the largest light REE resource in the Chilwa Alkaline Province in Malawi, clarifies the critical stages of REE mineralization in this deposit. The δ⁵⁶Fe values of most of the carbonatite lies within the magmatic field despite variations in the proportions of monazite, ankerite, and ferroan dolomite. Exsolution of a hydrothermal fluid from the carbonatite melts is evident based on the higher δ⁵⁶Fe of the fenites, as well as the textural and compositional zoning in monazite. Field and petrographic observations, combined with geochemical data (REE patterns, and Fe, C, and O isotopes), suggest that the key stage of REE mineralization in the Kangankunde carbonatite was the late magmatic stage with an influence of carbothermal fluids i.e. magmatic–hydrothermal stage, when large (~200 µm), well-developed monazite crystals grew. The C and O isotope compositions of the carbonatite suggest a post-magmatic alteration by hydrothermal fluids, probably after the main REE mineralization stage, as the alteration occurs throughout the carbonatite but particularly in the dark carbonatites.

Elevated antimony concentrations in aqueous environments from anthropogenic sources are becoming of global concern. In this respect iron oxides are known to strongly adsorb aqueous antimony species with different oxidation states, but the effect of silica on the removal characteristics is not well understood despite being a common component in the environment. In this study, ferrihydrite was synthesized at various Si/Fe molar ratios to investigate its adsorption and co-precipitation behaviors with aqueous antimony anionic species, Sb(III) and Sb(V). The X-ray diffraction analyses of the precipitates showed two broad diffraction features at approximately 35° and 62° 2θ, which are characteristics of 2-line ferrihydrite, but no significant shifts in peak positions in the ferrihydrite regardless of the Si/Fe ratios. The infrared spectra showed a sharp band at ~930 cm⁻¹, corresponding to asymmetric stretching vibrations of Si–O–Fe bonds which increased in intensity with increasing Si/Fe molar ratios. Further, the surface charge on the precipitates became more negative with increasing Si/Fe molar ratios. The adsorption experiments indicated that Sb(V) was preferentially adsorbed under acidic conditions which decreased dramatically with increasing pH while the adsorption rate of Sb(III) ions was independent of pH. However, the presence of silica suppressed the adsorption of both Sb(III) and Sb(V) ions. The results showed that Sb(III) and Sb(V) ions were significantly inhibited by co-precipitation with ferrihydrite even in the presence of silica by isomorphous substitution in the ferrihydrite crystal structure.