Search Results (31)

Mining and metallurgical residues represent one of the largest untapped secondary raw-material resources in Europe; however, their critical raw material (CRM) potential remains insufficiently quantified. This study applies a comprehensive mineralogical, geochemical, and geostatistical framework to evaluate nine distinct waste types from the Cartagena–La Unión Mining District (SE Spain), a historically exploited polymetallic system. A total of 79 samples were analysed using X-ray diffraction, wavelength-dispersive X-ray fluorescence, and advanced multivariate statistical techniques (correlation analysis, principal component analysis and hierarchical clustering) to identify geochemical associations controlling CRM distribution. The results reveal strong geochemical heterogeneity, with systematic enrichment in Co, Ni, Cu, Ga, Nb, and rare-earth proxies. Three dominant geochemical controls were identified: (i) a lithogenic silicate association governing Al–Si–Ti–Nb patterns, (ii) a sulphide-derived metalliferous association characterized by Cu–As–Sb, and (iii) an oxidation–adsorption association responsible for Ga–Y affinity. Several CRM concentrations approach or exceed typical global ore grades for secondary resources, particularly in flotation-derived and oxidation-rich residues. Geostatistical modelling confirms spatially coherent CRM hotspots, with base-metal enrichment linked to sulphide relics and Ga–Nb–Y controlled by Fe–Mn oxyhydroxides. Environmental assessment indicates potential metal mobility under acidic conditions, while also highlighting significant remediation benefits associated with residue reprocessing. Taken together, this study provides a robust and reproducible methodology for CRM assessment in legacy mining wastes and identifies priority residue types within the district with the highest strategic recovery potential. Full article

This study presents the first stream-sediment geochemical survey conducted in the western Oecusse enclave (Timor-Leste), aiming to identify geochemical anomalies associated with potential metallic mineralization in a region where mineral occurrences remain poorly documented. A total of 27 stream-sediment samples were collected from first- and second-order drainage systems and analysed for a multi-element suite using ICP-MS and INAA. Robust statistical approaches, including univariate analysis, median absolute deviation (MAD), Tukey boxplot thresholds, and compositional data analysis combined with principal component analysis (CLR–PCA), were applied to identify anomalous geochemical associations. To improve statistical robustness, PCA was performed on reduced and process-oriented variable sets. The results reveal significant geochemical variability, with maximum concentrations reaching 214 mg/kg for As, 142 mg/kg for Co, 27,220 mg/kg for Cr, 437 mg/kg for Cu, 1520 mg/kg for Ni, 67 mg/kg for Pb and 267 mg/kg for Zn. Multivariate analysis distinguishes two main geochemical signatures. The first association (Co–Cr–Ni–Mg–Fe) reflects a strong ultramafic geochemical signal consistent with contributions from mafic to ultramafic lithologies documented in the region. The second association (As–Bi–Cu–Pb–S–Sb–Se–Tl–Zn) indicates polymetallic enrichment commonly observed in sulphide-related geochemical systems. The spatial distribution of these geochemical signals highlights localized drainage basins exhibiting relative enrichment patterns. These results demonstrate the effectiveness of stream-sediment geochemistry as a first-pass exploration tool and provide new geochemical constraints for geological interpretation and future mineral exploration in Timor-Leste. The approach demonstrates the value of integrated geochemical and statistical methods for mineral exploration in data-poor regions. Full article

Waste deposits from the Iberian Pyrite Belt that are rich in pyrite are a valuable secondary resource for getting back sulphide minerals and important metals that go with them. This study assessed the efficacy of a Multi-Gravity Separator (MGS) in concentrating pyrite and related polymetallic minerals from sulphide waste material sourced from the Alonso mining district (Huelva, Spain). Bench-scale MGS tests were done on two particle size fractions (−500 µm and −50 µm) to see how the speed of the drum rotation, the angle of the tilt, and the flow rate of the wash water affected the separation efficiency. Mineral Liberation Analysis (MLA) showed that both size fractions had about 65.8 wt% pyrite, but the −50 µm fraction was much more liberated. Under the best operating conditions, the MGS was able to recover about 58% of the pyrite from the −500 µm fraction and about 64% from the −50 µm fraction. The mass recoveries were about 38% and 42%, respectively. There was also a better recovery of related metals like Co, Cu, Zn, and Mn, especially for the finer fraction. This shows the improvement of the liberation and stratification behaviour. The results show that MGS is a good way to pre-concentrate fine-grained pyrite-rich waste. The performance is heavily influenced by the size distribution of the particles and the operating parameters. These results suggest that improvements in gravity separation may offer a long-term pathway for the recycling of sulphide mine waste within a circular economy. Full article

The optimization of enrichment zones for Co-rich crusts involves multiple factors such as crust thickness, elemental content, topography, slope, and biological distribution, making it a complicated research endeavor. Based on survey data from the contract area, the present study pioneers the integration of environmental factors into enrichment zone selection. It conducts a comprehensive analysis of resource, environment, and mining considerations, alongside optimization methodologies. Quantitative indicators for resource, environment, and mining are spatially correlated and assigned to corresponding grid cells. A weighted scoring method is proposed to compare enrichment zone selection results under different weightings, finally forming the optimal enrichment zone selection scheme. This scheme fully achieves the maximization of resource reserves, the protection of biological communities, and the safeguarding of future mineral development. It also provides technical reference for enrichment zone selection of deep-sea minerals such as polymetallic nodules and hydrothermal sulphides. Full article

The novelty of this study lies in the first comparative characterisation of five carbonaceous materials: three monophase carbons (wood charcoal, carbon, graphite) and two ore-derived CM samples from polymetallic sulphide and oxidised lithium ores. The methodology included IR spectroscopy, XPS, acid–base adsorption centres identified by colour indicators, chemical composition analysis, and kinetic flotation tests. Bulk and surface compositions differed significantly: although the ash content of ore-derived CM reached 84.4%, XPS revealed carbon-enriched surfaces with thin films of about 1–2 nm. IR spectra confirmed multiphase structures with carbonate, silica, and aluminosilicate bands, and showed an identical composition of CM from different industrial ore types. Flotation kinetics confirmed high floatability (recoveries 80%–99%, k up to 1.95 min⁻¹). Even with sodium lignosulphonate at 500 mg/L, recovery only decreased from 83.02% to 52.54%, showing the limited efficiency of depressants. These results provide a basis for the preliminary removal of CM prior to rough (bulk) flotation in the processing of different ore types, improving concentrate quality, reducing reagent consumption, and lowering metallurgical losses. Full article

The Arabian–Nubian Shield (ANS) hosts numerous volcanogenic massive sulphide (VMS) deposits formed in submarine volcanic settings and enriched by hydrothermal processes, making it a critical region for mineral exploration due to the types of deposits it hosts and its geological complexity. The Wadi Bidah Mineral Belt (WBMB), located within the Arabian Shield, contains over 30 polymetallic VMS occurrences associated with an island arc system active between 950 and 800 million years ago. Despite its mineral potential, the WBMB still needs to be explored, with limited geophysical studies to support resource evaluation. This study focuses on the Hawiah area, a prominent VMS site within the WBMB, to delineate subsurface mineralization using transient electromagnetic (TEM) methods. TEM surveys were conducted to characterize the conductivity structure and identify potential zones of sulphide mineralization. Data were processed and inverted to generate 1D, 2D, and 3D resistivity models, providing critical insights into the depth, geometry, and continuity of the mineralized zones based on the final 3D resistivity distribution. The results revealed distinct conductive (very low resistivity) anomalies, correlating with known surface gossans and inferred sulphide-rich layers, and extended these features into the subsurface. The integration of TEM results with geological and geochemical data highlights the effectiveness of this approach in detecting and mapping concealed mineral deposits in complex geological environments. This study advances the understanding of VMS systems in the WBMB and demonstrates the potential of TEM surveys as a key tool for mineral exploration in the Arabian Shield. Full article

As challenges in precious and base metal exploration intensify due to the diminishing availability of high-grade ore deposits, rising demand, energy costs, and stricter regulations towards net-zero carbon activities, advanced techniques to enhance exploration efficiency are becoming increasingly critical. This study demonstrates the effectiveness of quantitative X-ray diffraction (QXRD) with Rietveld refinement, coupled with multivariate statistical analysis (including agglomerative hierarchical clustering, principal component analysis, and fuzzy analysis), in characterizing the complex mineralogy of strata-bound volcanic-associated limestone-skarn Zn-Pb-Ag-(Cu-Au)-type sulphide deposits (SVALS). Focusing on 113 coarse rejects from the Gumsberg project located in the Bergslagen mining district in central Sweden, the research identified five distinct mineralogical clusters corresponding to polymetallic base metal sulphide mineralization, its proximal alteration zones, and variably metamorphosed host rocks. The results reveal significant sulphide mineralization, ranging from disseminated to massive occurrences of sphalerite, pyrrhotite, pyrite, and galena, with trace amounts of secondary minerals like anglesite in certain samples indicating weathering processes. The study also identifies rare minerals such as armenite, often overlooked in traditional geological logging. These findings underscore the potential of QXRD to enhance resource estimation, optimize exploration strategies, and contribute to more efficient and sustainable mineral exploration programs. The accuracy of QXRD was cross-validated with geological logs and geochemical data, confirming its reliability as a mineralogical discrimination tool. Full article

The Batailing Au deposit is a vein-type deposit in central Jilin Province, situated in the southern sector of the Lesser Xing’an–Zhangguangcai Range within the eastern Central Asian Orogenic Belt. NE-trending fault-controlled orebodies occur in the Upper Permian Yangjiagou Formation and quartz diorite–porphyrite. The mineralisation process was delineated into three stages: (I) quartz–arsenopyrite–pyrite, (II) quartz–polymetallic sulphides (main Au mineralisation stage), and (III) quartz–pyrite–carbonate. Fluid inclusions (FIs) in quartz were identified as four types: PC-type (pure CO₂), C₁-type (CO₂-bearing), C₂-type (CO₂-rich), and W-type (aqueous two-phase). Raman spectroscopy analysis revealed that the vapor components of the FIs predominantly comprised CO₂ with minor quantities of CH₄ in stages I–II. Stages I and II encompassed four types of FIs with homogenisation temperature ranging from 264 to 332 °C and 213 to 292 °C and salinity spanning from 4.7 to 11.2 wt% and 1.8 to 11.6 wt%, respectively. Stage III exclusively contained W-type FIs with homogenisation temperature ranging from 152 to 215 °C and salinity spanning from 1.4 to 6.4 wt%. H-O isotopic values (δD = −84 to −79.6‰, δ¹⁸O_H2O = 6.2 to 6.4‰ in stage I and δD = −96.4 to −90.4‰, δ¹⁸O_H2O = 2.8 to 4.4‰ in stage II) and microthermometric data indicated that the ore-forming fluids are initially from a magmatic source, with later meteoric water input. Low C isotopic data from CO₂ in FIs in quartz (−24.4 to −24.3‰ in stage I and −23.7 to −22.6‰ in stage II) indicated an organic carbon source. Ore precipitation is mainly attributable to fluid immiscibility. S-Pb isotopic data (δ³⁴S = −3.5 to −1.6‰; ²⁰⁶Pb/²⁰⁴Pb = 18.325–18.362, ²⁰⁷Pb/²⁰⁴Pb = 15.523–5.562, ²⁰⁸Pb/²⁰⁴Pb = 38.064–38.221) revealed that ore metals primarily originated from magma. Based on this research, the origin of the Batailing Au deposit is of the mesothermal magmatic–hydrothermal lode type. Full article

This short paper analyses the concentrations of two major components (Fe, S) and eight trace elements (As, Au, Co, Cu, Hg, Ni, Mn, Zn) in soils and tailings from Tierra Amarilla (northern Chile) using ICP-Ms analysis. The levels of As, Au, Cu, Fe and S are very high and come from polymetallic sulphides from nearby mines, together with minor contributions of Co, Ni and Mn. Hg has its origin in the extreme seasonal flows of the Copiapó River, which erodes the dumps of old precious metal mines. These high concentrations require further analysis of possible metal immobilisation techniques, bioavailability or analysis in cultivated plants. Full article

Variations in the recovery of platinum group metals (PGMs) are often attributed to mineralogical and other natural ore-type variations. To increase the recovery of PGMs by the flotation process, a comprehensive understanding of gangue and valuable minerals is essential for optimising the extraction and processing of metals. Recoveries may be improved if the questions of how, where, and why losses occur can be answered with a certain degree of confidence. A requirement is the availability of statistically reliable mineralogical data. The PGMs of MG-1–4 chromite tailings dumps of the western limb of the Bushveld complex (BC) were studied in detail to unravel the PGMs and the nature of the platinum group minerals in the sample. Characterisation of the chromite tailings via deportment analysis revealed that the sample contained a significant amount of 3E PGM + Au (Pt, Pd, Ru, and Au) and was concentrated in the -25 µm fraction. The results of automated mineralogical analysis showed that the sample was composed of the PGE-sulphides group, comprising 63.6 vol%, PGE-sulfarsenides 10.4 vol%, PGE-arsenides 1.3 vol%, PGE-bismuth tellurides 3.3 vol%, PGMs-alloy 4.1 vol%, and Laurite comprising 17.3 vol% of the total PGE population. The sample was composed of 66.5 vol% of liberated PGMs, 0.2 vol% attached to liberated BMS, 27.3 vol% of PGMs attached to or locked within silicate or oxide gangue composite particles, 0.2 vol% of PGMs associated with BMS attached to silicate or oxide gangue particles, and a low proportion (5.8 vol%) of PGMs reported being locked within gangue or oxide particles. The majority of PGM grains observed were reported in the fast-floating category (64.4 vol%), 27.6 vol% in the slow-floating 1 category, 2.2 vol% in the slow-floating 2 category, and 5.8 vol% to the non-floating category. The results of the study revealed that the PGMs of MG 1–4 chromite tailings were liberated; however, the low liberation index (<0.2) suggested that a significant portion of PGMs remained trapped within gangue, hindering their recovery. This highlights the need for effective comminution (crushing and grinding) to achieve better liberation. The sample contained fine particles that were more prone to being lost in the tailings and to lowering recovery due to the slimes coating valuable minerals. The recovery of the PGMs from this complex’s polymetallic bodies of low-grade and complex mineralogy will be insufficient with traditional methods and thus innovation is needed. Innovation like advanced comminution, novel flotation equipment or reagents, selective leaching and bioprocessing can overcome these challenges. Full article

The study object was slag from the Balkhash copper smelter, obtained by re-melting anode mud containing nonferrous metals. The process flow for processing these slags includes sintering with Na₂SO₄, Na₂CO₃, and coal, followed by soda-alkaline leaching of the sinter and extraction of metals from the solution into marketable products. Since sintering is the main operation providing high selectivity, the composition of the products of this process was studied. The main transformations during sintering were determined, and the optimal parameters were identified. The structures of slags and sintered materials obtained during the experiments were studied by electron-probe microanalysis. Sintering was performed at 600–800 °C. The best results for sulphidization of slag components were obtained at 800 °C; a further increase in temperature leads to the smelting of sinter particles and slows down sulphidization. The optimal quantities of additives, based on the weight of the slag, are Na₂SO₄—45%, Na₂CO₃—15%, and reducing agent—41%, with a sintering time of 2 h. These conditions enable the sulphidization of non-ferrous metals in the slag to the entire depth of the polymetallic globules. The distinct concentration of harmful impurities (Ni, As, and Sb) was observed in the fine structure of the polymetallic globules. Full article

A comprehensive hydrogeochemical survey of the geothermal waters from the Nappe Zone (Maghrebides fold-and-thrust belt) was undertaken to determine the origins of geothermal waters and to assess the health risks associated with their potentially toxic elements. A total of 11 geothermal water and 3 stream water samples were collected and analysed for major and trace elements (As, B, Ba, Fe, Mn, Pb, Sr, Zn). Two main geothermal water groups were highlighted by hydrogeochemical diagrams and multivariate analyses (PCA, HCA): the first group is the Na−Cl type, TDS > 10 g/L, controlled by deep circulation, while the second group is the Na-Cl−HCO₃ type, TDS < 2 g/L, and controlled by shallow circulation. A curved hydrogeochemical evolution path, observed from mixed bicarbonate shallow groundwater to chloride geothermal water, indicates that the interaction with evaporites drives the chemistry of the geothermal samples. On these, the As enrichments come from sulphide oxidation polymetallic mineralisation during the upwelling to the surface from E–W major lineaments. Therefore, E–W lineaments are potential areas for mineral prospecting. The health risk assessment reveals that the concentration of potentially toxic elements in geothermal waters are lower than the guideline values for the protection of freshwater aquatic life and dermal exposure (bathing or balneology). Full article

The Wawa Gold Corridor, a series of Archean orogenic Au deposits in the Michipicoten greenstone belt, Canada, comprises two styles of Au mineralization: (1) syn-deformation gold associated with pyrite and arsenopyrite; and (2) late- to post-deformation gold associated with chalcopyrite and Bi-Te(-S) phases. Through petrographic and mineral–chemical analysis, it was determined that gold in the latter assemblages precipitated from Bi-rich polymetallic melts during hydrothermal overprinting of the earlier Au-As-S mineralization; this event was likely driven by the emplacement of Archean lamprophyres. The formation and evolution of these melts was governed by fluid–pyrite reaction interfaces, where the bulk composition of the melts was broadly controlled by the trace-element chemistry of the sulphide minerals in the local host rocks. This suggests that the melt-formation event involved mobilization of existing metal endowments related to early Au events, rather than addition of new Au, Bi, and Te. Thus, the deposition of high-grade Au by Bi-rich melts was dependent on pre-existing sulphide mineralization, both as a source of metals and as micro-environments that stabilized the melts. The paragenesis documented in the Wawa Gold Corridor (i.e., early hydrothermal Au-As-S mineralization and late melt-related Au-Bi-Te mineralization) has been previously recognized in numerous other orogenic and non-orogenic Au deposits. Herein, it is suggested that this apparent consistency in the timing of melt events across multiple systems probably reflects the physicochemical conditions (i.e., fO₂-aH₂S) of orogenic fluids being incompatible with molten Bi. Bi-rich polymetallic melts are hence unlikely to form primary Au mineralization in orogenic systems but can, however, have a significant impact on the ultimate deposit-scale distribution of Au via secondary mobilization and enrichment. Full article

Geological and radiometric studies of outcrops aided by extensive subsurface exploration through drill holes in an otherwise soil-covered terrain revealed the existence of low grades, medium tonnage, and metasomatite types of polymetallic uranium deposits at Rohil in India. Microscopic studies, electronprobe micro analyses, and geochemical analyses of samples from lodes indicate the polymetallic nature of mineralisation involving copper and molybdenum, in addition to uranium. Wide variations in the composition of fluid (S-, F-, P-, and O-rich) led to the formation of sulphides, fluorite, U-phosphosilicate, quartz, and magnetite, respectively, and are associated with uraninite. Litho-geochemical analyses from the Rohil deposit indicate multifarious metasomatic alterations associated with polymetallic mineralisation occurring in veins. The major mineralogical and metasomatic controls on rock compositions and the extent of material transfer processes that influenced the host rocks and mineralisati on are quantified by molar element ratio studies and alteration plots. General element ratio (GER) diagrams on chemical analyses of rock samples reveal albitisation and chloritisation as major and microclinisation, sericitisation, carbonatisation, and silicification as minor wall rock alterations associated with ore mineralisation. The alteration box plot between the chlorite–carbonate–pyrite index (CCPI) and the Ishikawa alteration index (AI) indicates the influence of hydrothermal activity and dominance of both albitisation and chloritisation. The ore zone is controlled by meso- and microstructures and the geometry of the soda- and potash-metasomatised zone around hydrothermal veins. This zone contains several anastomosing mineralised veins defined by a prominent joint that is set in quartzite that strikes subparallel to the axial surface of the F₂ isoclinal folds and the pervasive schistosity S₁ in the quartz–feldspar–biotite schist. Aventurisation of albite and microcline, established through electron probe micro analyses, can be considered as a pathfinder for uranium mineralisation. The close association of uranium and metallic sulphide mineralisation with microstructural, mineralogical (albitisation, chloritisation, and microclinisation), and geochemical variations can be applied as suitable exploration guides in a similar geological set-up worldwide. Full article

We provide an updated overview of the known mineral deposits from the Sila and Serre Massifs in Calabria, contributing to setting their genesis within a complex geologic history, starting from the late-Carboniferous. We summarize the mineralization reported in the literature, with a critical review of the host tectonic units, by taking into account the upgrades in the knowledge of these areas. We also set them in updated geological maps and in stratigraphic columns, highlighting the crustal levels to which they pertain. Despite the geologic and minerogenetic similarities potentially existing with late- to post-Variscan mineral deposits from other regions (e.g., Sardinia and French Central Massif), the scientific literature on the Calabria mineralization is out-of-date and not exhaustive. Moreover, these ore deposits were likely considered not economically attractive enough to stimulate new scientific studies. However, in our opinion, such studies are needed to resolve the main open questions, which rely on deciphering the origin and age of mineralization. Finally, research for critical elements hosted by the Sila and Serre mineralization (e.g., In, Ge and Ga in sphalerites) is a possible interesting new perspective. Full article