Search Results (370)

Efficient recovery of critical metals from complex polymetallic ores relies on clarifying their mineralogical occurrence. A Cd-Ag-rich Pb-Zn ore from southwestern China was investigated via a multi-scale process mineralogy approach integrating reflected-light microscopy, TIMA and LA-ICP-MS. Systematic analysis was conducted on ore texture, mineral liberation characteristics, and the occurrence and distribution of Ag and Cd. The ore is a medium–low grade Pb-Zn deposit (Pb 0.81%, Zn 4.33%) with economically recoverable associated Cd (0.066%) and Ag (5.04 ppm), dominated by sphalerite (7.74%), galena (1.39%), pyrite (3.92%), quartz (47.80%) and calcite (18.66%). TIMA analysis revealed poor liberation of sphalerite and galena, with fully liberated particles accounting for <30%. LA-ICP-MS results showed that Cd is highly enriched in sphalerite (average 5982 ppm, 98%) mainly in isomorphous form, while Ag is dispersed in pyrite (average 178 ppm, 56%), galena (average 227 ppm, 25%) and sphalerite (average 31 ppm, 19%), also primarily as isomorphs; partial Cd in pyrite occurs as micro-inclusions. The multi-scale mineralogical data provide a scientific basis for resource utilization, indicating the necessity of fine grinding and differentiated recovery strategies: “zinc depression followed by lead flotation” for Pb-Zn recovery, the establishment of a comprehensive Ag recovery system with Pb-Zn-Fe as carriers for Ag recovery, and “Zn-carried Cd” flotation for Cd recovery. This study verifies the effectiveness of combined TIMA and LA-ICP-MS in elucidating critical metal occurrence, and provides a mineralogy-based process design for the sustainable processing of such complex ores. Full article

Hydrothermal cobalt (Co) deposits are a significant source of Co; however, the sources of Co and hydrothermal fluids for such deposits remain poorly understood. This study addresses this issue through an investigation of the geology, mineralogy, and in situ sulfur isotopes of the Qibaoshan Co-Pb-Zn-Cu deposit, a typical hydrothermal Co deposit in South China, to constrain the occurrence of Co and the sources of Co and hydrothermal fluids. Detailed scanning electron microscopy (SEM), TESCAN Integrated Mineral Analyzer (TIMA), and electron microprobe (EPMA) mapping analyses reveal that Co in the Qibaoshan deposit occurs predominantly as Co-bearing minerals in veinlet mineralization, mainly including cobaltite, skutterudite, and smaltite. EPMA elemental mappings reveal that cobaltite grains commonly show a compositional evolution from Ni-S-rich and As-Fe-poor cores to As-Fe-rich and Ni-S-poor rims. This evolution indicates a decrease in fluid temperature and Ni content, coupled with an increase in the As/S ratio during ore-forming processes. In situ S isotope analyses of various sulfides (pyrite, chalcopyrite, sphalerite, galena, and arsenopyrite) yield a wide range of δ³⁴S_V-CDT values from 0.24‰ to 19.08‰, with two dominant clusters at 2–5‰ and 15–17‰. This suggests two end-member sources for sulfur and hydrothermal fluids in the Qibaoshan deposit: magmatic and sedimentary sources. Arsenopyrite, which is closely associated with Co minerals, yields δ³⁴S_V-CDT values ranging from 2.17‰ to 5.99‰, pointing to a magmatic origin for Co in the Qibaoshan deposit. The Pb-Zn and Cu mineralization of the deposit was also likely mainly derived from magmatic sources, with the incorporation of sedimentary sulfur and fluids during the ore-forming processes. This study demonstrates that magmatic–hydrothermal fluids derived from depth can serve as sources of Co, even in hydrothermal deposits where no magmatic rock is exposed, which provides crucial implications for the metallogenic models and mineral exploration of hydrothermal Co deposits. Full article

The Kocayayla Pb–Zn ± Cu vein-type mineralization is located in the Biga Peninsula, northwestern Türkiye. This study aims to constrain the geological, geochemical, and isotopic characteristics of the mineralization and to clarify its genetic classification. The deposit is hosted mainly by andesitic and basaltic andesitic rocks as well as schists and is structurally controlled by E–W-trending strike-slip faults. Mineralogical and petrographic identifications, XRD analyses, whole-rock geochemistry, and sulfur isotope data were integrated to evaluate ore-forming processes. Mineralization is temporally and spatially associated with propylitic and phyllic to argillic alteration and is concentrated within zones of intense silicification and chloritization, accompanied by quartz, sericite, kaolinite/nacrite, chlorite, and carbonate assemblages. The ore assemblage is dominated by galena, sphalerite, and subordinate chalcopyrite, with minor fahlore-group minerals. Rare earth element patterns of ore samples (whole rock) overlap with those of the wall rocks, whereas Pb–Zn enrichment reflects selective hydrothermal metal transport. Sulfur isotope compositions show limited internal variation and indicate sulfur derived predominantly from H₂S-dominated magmatic–hydrothermal fluids. Regional comparison of δ³⁴S datasets and reported Au contents across the Biga Peninsula indicates that Au-rich intermediate-sulfidation epithermal systems exhibit broader and more variable sulfur isotope ranges, whereas Au-poor intermediate-sulfidation epithermal systems show relatively restricted and near-zero δ³⁴S values. These features collectively support the classification of the Kocayayla mineralization as an Au-poor intermediate-sulfidation epithermal Pb–Zn system. Full article

In this work, hexagonal wurtzite ZnS nanorods (NRs) and cubic sphalerite ZnS quantum dots (QDs) were synthesized via different methods, and then ZnS NRs/rGO and ZnS QDs/rGO nanocomposites were fabricated by a hydrothermal composite strategy. The structural, morphological, optical and photocatalytic properties of the as-prepared samples were systematically characterized by XRD, TEM, HRTEM, XPS, FT-IR, UV-Vis absorption and PL spectroscopy. The photocatalytic performance of all samples was evaluated by the degradation of methylene blue (MB) under ultraviolet (UV) irradiation, and the cyclic stability of the catalysts was also investigated. The results showed that rGO effectively inhibited the agglomeration of ZnS nanostructures, promoted the separation of photogenerated electron–hole pairs and suppressed their recombination. ZnS QDs/rGO exhibited the optimal photocatalytic performance with an MB degradation efficiency of 98.08% and a first-order rate constant of 2.063 × 10⁻² min⁻¹ after 180 min of UV irradiation, which was significantly higher than pristine ZnS NRs (74.49%, 7.58 × 10⁻³ min⁻¹) and ZnS QDs (88.95%, 1.47 × 10⁻² min⁻¹). Moreover, ZnS NRs/rGO showed superior cyclic stability due to the higher crystallinity of ZnS NRs. The enhanced photocatalytic activity and stability of ZnS/rGO nanocomposites were attributed to the synergistic effect between ZnS and rGO, which increased active sites, facilitated charge transfer and inhibited photocorrosion. This study provides a valuable structural design strategy for the development of high-efficiency ZnS-based photocatalysts for organic dye degradation in water treatment. Full article

The Bagenheigqier medium-sized Pb-Zn deposit is located in central-southern segment of Great Xing’an Range, northeastern China, where its vein-type orebodies are hosted within the structural contact zone between the Lower Permian Dashi Formation and granite porphyry intrusions. Five mineralization stages are divided into skarn (I), oxide (II), quartz-pyrite-arsenopyrite (III), quartz-polymetallic sulfide (IV), and quartz-calcite-pyrite (V). Three types of fluid inclusions (FIs) are identified in Bagenheigeqier Pb-Zn deposit, including daughter mineral-bearing three-phase (SL-type), vapor–liquid two-phase (VL-type), and vapor-rich two-phase (LV-type) FIs. All FI types occur in Stages I–III, with homogenization temperatures (Th) of 423–486, 389–441, 362–408 °C, and salinities of 1.1–49.2, 0.9–43.9 and 0.9–38.8 wt.% NaCl equiv, respectively. Stage IV hosts only VL- and LV-type FIs (Th: 277–319 °C; salinity: 2.1–8.7 wt.% NaCl equiv), whereas Stage V contains exclusively VL-type FIs with Th of 173–214 °C and salinity of 1.2–5.7 wt.% NaCl equiv. The H-O isotopic results of quartz in stage II–IV (δD = −103.5‰–−99.1‰, −115.7‰–−107.8‰ and −121.5‰–−117.2‰; δ¹⁸O_H2O = 4.4‰–7.1‰, 1.1‰–3.5‰ and −4.6‰–−3.5‰) indicate the ore-forming fluids are predominantly of magmatic origin with subordinate meteoric water mixing. Fluid boiling and the mixing of meteoric water may lead to the precipitation of metal. The in situ trace elements analyses indicate that sphalerites in main mineralization stage are enriched in Fe, Mn, Co and In and depleted in Ga and Ge. The calculation results suggest that the sphalerites crystallized under moderate temperature conditions (286–330 °C) and intermediate f_S2 (−10.5 to −9.2) conditions. The geological, fluid inclusion, isotopic and trace element evidences indicate that the Bagenheigeqier deposit is classified as a skarn-type deposit. Full article

Ultrasmall near-infrared (NIR)-responsive quantum dots (QDs) are highly promising for deep-tissue phototherapy but often face challenges with biocompatibility and clearance. In this study, Cu₂ZnSnS₄ quantum dots (CZTS QDs) were synthesized via a non-injection method and surface-functionalized with glutathione (GSH) to create water-dispersible and biocompatible CZTS@GSH QDs. Comprehensive characterization using XRD, TEM, DLS, XPS, and UV-Vis spectroscopy confirmed a sphalerite-type ZnS crystal structure, an average hydrodynamic diameter of ~6.2 nm, and a band gap of 1.47 eV (843.5 nm). The CZTS@GSH QDs demonstrated effective photothermal conversion under 808 nm laser irradiation, achieving a temperature increase sufficient for photothermal therapy (PTT). Furthermore, using a DPBF assay, the QDs were shown to generate singlet oxygen, confirming their photodynamic therapy (PDT) capability. Owing to their ultrasmall size, strong NIR absorption, and demonstrated dual PTT/PDT functions, the CZTS@GSH QDs are established as a nanoplatform with potential for combined cancer treatment. Full article

Kutná Hora ore district, one of the largest historical silver deposits in Central Europe, consists of nine major lodes with Pb-Zn-Ag mineralization hosted by high-grade basement rocks of the Kutná Hora Crystalline Complex in central part of the Bohemian Massif. We conducted a detailed electron-microprobe study of a previously unknown ore mineralization from the uppermost level of the Muzejní důl mine, which is a medieval mine located within the Ag-richest Oselské pásmo Lode, in the southern part of the ore district. An unusual nature of this ore mineralization, which originated during three respective stages, was found. The early stage comprises the hypogene mineralization commonly occurring in the southern part of the district, composed of pyrite, arsenopyrite, Fe,Mn-enriched sphalerite, galena, and (keno)argentotetrahedrite-(Fe) hosted in quartz and siderite-rhodochrosite gangue. The second stage was characterized by the corrosion of early vein fill followed by the crystallization of a specific suite of ore minerals anomalously enriched in Ag, Cu, Zn, Cd, As, and Sb, including galena, Cd-enriched and Fe-poor sphalerite, greenockite, bornite, Ag,As,Sb,Mn-bearing chalcopyrite, silver, gold, stephanite, As,Cu-bearing pyrargyrite, Ag-Cu- and Sb-As-bearing polybasite-pearceite group minerals and a suite of tetrahedrite-group minerals, the latter showing wide variations in Ag-Cu, Sb-As, and Fe-Zn-Cd contents. The origin of the second-stage mineralization is interpreted in hydrothermal remobilization of ore metals and metaloids from the early ore mineralization, which was mediated by surficial fluids characterized by elevated redox potential. The third stage comprises acanthite and probably also Ag-Cu minerals (stromeyerite, jalpaite, and mckinstryite), Cu-S phases (covellite, spionkopite, geerite), and an Ag-Cu-Hg mineralization. This late mineralization was likely related to the pre-Cretaceous weathering of the apical part of the ore deposit and to the associated supergene enrichment of deeper parts of the ore zone by descending Ag,Cu-bearing waters. Full article

The Lanuoma sediment-hosted lead–zinc (Pb–Zn) deposit, situated in the central part of the Sanjiang base metal metallogenic belt (SMB) within the Changdu Basin, is hosted by Triassic Bolila Formation limestone. The source of metals and sulfur (S), as well as the ore-forming processes for the deposits in this belt, are contentious. To constrain the metal and sulfur sources and to define the ore-forming mechanism, we analyzed Zn, Pb, and S isotopes of sphalerite and robinsonite, as well as Zn isotopes of the host limestone and the metamorphic basement. Sphalerite shows homogeneous δ⁶⁶Zn values (−0.31‰ to −0.12‰; mean = −0.20‰). The calculated δ⁶⁶Zn of the ore-forming fluid (~0.00‰) matches that of the Triassic limestone, indicating a sedimentary Zn source (δ⁶⁶Zn = −0.11‰ to −0.09‰; average 0.00‰). Robinsonite displays a wider δ⁶⁶Zn range (−0.22‰ to 0.44‰), reflecting a mixture of sedimentary and metamorphic sources (δ⁶⁶Zn = 0.12‰ to 0.42‰; average 0.22‰). Lead isotopes of sphalerite are uniform (²⁰⁶Pb/²⁰⁴Pb = 19.041–19.079) and indicative of a sedimentary rock source, whereas robinsonite shows wide variation (²⁰⁶Pb/²⁰⁴Pb = 19.070–19.156) and linear trends between low- and high-radiogenic end-members, indicating mixed Pb sources from sedimentary rocks and metamorphic basement. Sulfur isotopic compositions of sulfides (δ³⁴S = −1.4‰ to 2.6‰; mean = −0.1‰) cluster near 0‰, consistent with a deep magmatic origin. A strong linear correlation between ²⁰⁶Pb/²⁰⁴Pb and δ⁶⁶Zn, coupled with a lack of correlation between both ²⁰⁶Pb/²⁰⁴Pb and δ³⁴S and δ⁶⁶Zn and δ³⁴S in the sulfides, indicates that Pb and Zn were derived from a common metal source, whereas sulfur originated from a distinct reservoir. Combined with previously published fluid inclusion, rare earth element, and multi-isotopic constraints, these results suggest that Pb–Zn mineralization at Lanuoma was controlled by a mixing between metal-rich basinal brines and sulfur-rich deep-sourced fluids, leading to sulfide precipitation dominated by open-space filling. This study provides new insights into the genesis and mineralization process of sediment-hosted Pb–Zn deposits in the Sanjiang metallogenic belt. Full article

The Sichuan–Yunnan–Guizhou Pb-Zn metallogenic belt (SYG metallogenic belt), a crucial metallogenic unit on the southwestern margin of the Yangtze Block, is a key part of the South China low-temperature metallogenic domain. The incorporation mechanisms and distribution of trace elements (e.g., Ge, Ga, Cd) widely enriched in Pb-Zn sulfides throughout this region remain poorly understood. This study investigates main-ore-stage sulfides (sphalerite and pyrite) from the Maoping Pb-Zn deposit using in situ laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) analyses and mapping to systematically elucidate the partitioning and occurrence of these trace elements. The key findings are as follows: (1) Sulfides show distinct elemental partitioning: sphalerite preferentially concentrates Cd, Ag, Ge, Ga, and Se, whereas pyrite is significantly enriched in Mn, Ni, As, and Co. (2) Sphalerite is the primary host for many trace elements. Cadmium, Ge, Mn, Cu, and Ag mainly enter the sphalerite lattice by substituting for Zn²⁺. Coupled substitution mechanisms, such as Zn²⁺ ↔ Cd²⁺, 2Zn²⁺ ↔ Ge²⁺ + Cu²⁺, and 2Zn²⁺ ↔ Ga³⁺ + Cu⁺, facilitate the incorporation of Ge and Ga. (3) The sphalerite exhibits a trace element assemblage of high Cd-Ge and low Fe-Mn, which is geochemically similar to typical Mississippi Valley-type (MVT) deposits and differs significantly from sedimentary exhalative (SEDEX) and magmatic–hydrothermal deposits, indicating a medium- to low-temperature metallogenic environment. Based on these geochemical signatures and epigenetic textures, we confirm that the Maoping Pb-Zn deposit exhibits similarities with MVT deposits. Nevertheless, distinct differences in the tectonic setting and metal grades suggest it is a unique SYG-type Pb-Zn deposit. Full article

The Yawan gold deposit, located in the Western Qinling Orogen, contains gold mineralisation that is predominantly controlled by approximately east-west-trending fault systems. This study integrates field geology, petrography, cathodoluminescence imaging, electron probe microanalysis of gold-bearing minerals (pyrite and arsenopyrite), and in situ laser ablation U-Pb dating of calcite to constrain the timing of mineralisation and to elucidate the mechanisms of gold enrichment. This study reveals that the deposit is significantly structurally controlled and comprises two discrete mineralisation stages: a quartz-pyrite (Py1)-arsenopyrite (Apy1)-chalcopyrite assemblage (Stage 1), and a quartz-calcite-pyrite (Py2)-arsenopyrite (Apy2)-stibnite-sphalerite-galena assemblage (Stage 2). Py1 displays distinct zonation, with rim As contents notably higher than core values, while Co and Ni contents gradually decrease from core to rim. Py2 is characterised by high As (0.00%–4.72%), low Fe/S ratios, and a porous texture, containing gold and arsenopyrite inclusions. Invisible gold occurs in lattice-bound form in both Py1 and Py2. The As-Fe-S ternary diagram of pyrite indicates that Au⁺ likely entered the crystal lattice as a solid solution. Arsenopyrite geothermometry yields a mineralisation temperature of 389 ± 44 °C, and sulfur fugacity (ƒS₂) decreased markedly from Stage 1 to Stage 2. Combined with the S and Fe characteristics of pyrite, these features support a medium-temperature metamorphic hydrothermal environment. U-Pb dating of calcite from Stage 2 yields an age of 215.6 ± 7.1 Ma. In summary, the Yawan gold deposit belongs to the orogenic gold system, with its gold precipitation and enrichment controlled by sulfidation triggered by Late Triassic tectono-fluid activity. Full article

The Chaijiagou Mo deposit (0.11 Mt Mo @ 0.07%) is located along the northern margin of the North China Craton. This study integrates ore geology, S–Pb–He–Ar–H–O isotopes, and fluid inclusion (FI) analyses to constrain the sources of ore-forming fluids and metals, as well as mineralization mechanisms. Three principal inclusion types were identified: liquid-rich, vapor-rich, and saline FIs. Microthermometry documents a progressive decline in homogenization temperatures and salinities from early to late mineralization stages: Stage 1 (360–450 °C; 5.3–11.3 and 35.4–51.5 wt.% NaCl equation), Stages 2.1–2.2 (320–380 °C and 260–340 °C; 5.4–11.8 and 33.8–44.5 wt.% NaCl equation), and Stage 4 (140–200 °C; 0.4–3.9 wt.% NaCl equation). Noble gas and stable isotope data reveal that the ore-forming fluids were initially dominated by crustally derived magmatic–hydrothermal components with a minor mantle contribution, subsequently experiencing significant meteoric water input. S–Pb isotopic compositions demonstrate a genetic relationship between mineralization and the ore-bearing granite porphyry, indicating a magmatic origin for both sulfur and lead. Fluid–rock interactions and fluid boiling were the dominant controls on molybdenite and chalcopyrite deposition during Stage 2, whereas mixing with meteoric waters triggered galena and sphalerite precipitation in Stage 3. Full article

The Qingshan lead–zinc (Pb–Zn) deposit in northwestern Guizhou Province is a structurally controlled, carbonate-hosted system formed from basin-derived hydrothermal processes. Geology, fluid inclusion, and isotopic data reveal a multi-stage hydrothermal circulation after Emeishan Large Igneous Province (ELIP, ~260 Ma) tectono-thermal reactivation within the Sichuan–Yunnan–Guizhu triangle (SYGT) area. Fluid inclusion microthermometry indicates that ore-forming fluids were derived from deep sources influenced by enhanced crustal heat flow linked with possible thermal input from Indo-Caledonian tectonic activity after ELIP. Ore-stage calcite records mixed carbon derived from marine carbonates with additional inputs from organic matter and deep-sourced fluids, reflecting carbonate dissolution and fluid–rock interaction. Sulfide, together with fluid inclusion temperatures > 120 °C, indicates sulfur derived from evaporitic sulfate reduced by thermochemical sulfate reduction (TSR); the heavy sulfur signature and partial isotopic disequilibrium among coexisting sulfides reflect dynamic fluid mixing during ore deposition. Lead isotopes indicate metallogenic metals were leached mainly from Devonian–Permian carbonates with subordinate basement input. Ore precipitated by cooling, depressurization, and mixing of metal-rich, H₂S-bearing fluids in structurally confined zones where the carbonate–clastic interface effectively trapped ore-forming fluids, producing high-grade sphalerite–galena mineralization. Collectively, these data support a Huize-type (HZT) carbonate-hosted Pb–Zn genetic model for the Qingshan deposit. Full article

The mineral matter in coal has great significance for geological evolution, and clean and fractional utilization. The Laochang mining area is one of the largest anthracite coal production bases in Southern China, and the most important coal energy base in Yunnan province, China. This study investigates the composition and mode of occurrence of mineral matter in the Laochang coals to reveal the sediment provenance, sedimentary environment, and hydrothermal fluids. The predominant minerals in the Laochang coals include oxide (quartz, anatase), clay (kaolinite, illite/smectite mixed layer), sulfide (pyrite, sphalerite), phosphate (xenotime, monazite, goyazite–gorceixite), and carbonate (calcite, dolomite, sideroplesite, siderite). The minerals in the Laochang coals are dominated by quartz (2.4~54.8%) and kaolinite (3.4~39.2%), followed by illite, smectite, muscovite, calcite, pyrite, and anatase. Quartz and dolomite in SB-7+8 coal have the highest proportions, reaching 54.8% and 17.3%. The modes of occurrence of minerals reflect that the Laochang coals are affected by the epigenetic hydrothermal fluids and seawater. The chalcophile elements Hg, Pb, Se, and Cr, and lithophile elements Li, Nb, Ta, Zr, Hf, and REY are slightly enriched in XB-3 coal, which is attributed to the intrusion of seawater and the supply of terrestrial detrital materials, respectively. REY is dominated by LREY, followed by MREY, and a lower level of HREY in the Laochang coals, which have a high fractionation degree. The REY enrichment H-type is influenced by the hydrothermal fluids. Based on the relationship between Al₂O₃ and TiO₂, Al₂O₃/TiO₂ and Nb/Yb, and the negative anomaly Eu, the detrital material in the erosion source area of the Laochang coal is derived from the Emeishan Large Igneous Province basalt and felsic–intermediate rocks. Full article

The Wunuer deposit is an important hydrothermal Zn-Pb-Ag-Mo polymetallic deposit in the central Great Xing’an Range, NE China. The zinc–lead polymetal mineralization is closely hosted by the volcanic rocks of the Manketouebo formation (rhyolite and lithic crystal tuff) and related to the Mesozoic granite porphyry. Field evidence and petrographic observations have identified three mineralization stages within this deposit from deep to shallow: (1) late magmatic stage with vein-type Mo mineralization characteristics and mainly related to the deep granite porphyry; (2) magmatic–hydrothermal transition stage characterized by breccia-type Zn mineralization, which occurred within a steep cryptoexplosive breccia; and (3) hydrothermal stage featured by vein-type Zn-Pb-Ag mineralization hosted by the ore-bearing fractured zone. In this contribution, we present the mineralogy, zircon U-Pb age, sphalerite Rb-Sr dating, whole-rock geochemistry, and Hf-S-Pb isotopes of the Wunuer deposit. LA-ICP-MS zircon U-Pb dating of the ore-related granite porphyry, rhyolite, and lithic crystal tuff suggests that the Mo mineralization from the late magmatic stage occurred between 144.8 Ma and 145.8 Ma. The Rb-Sr isochron dating of sphalerite indicates that the hydrothermal stage Zn mineralization age is 121 ± 2.3 Ma, which is related to the volcanism of Baiyin’gaolao Formation in the Wunuer area. The concentrated and positive δ³⁴S_V-CDT values (0.17‰~5.40‰) of sulfides, as well as uniform Pb isotope compositions of granite porphyry intrusion and galena, jointly imply a magmatic source of metallogenic materials for Pb-Zn mineralization. Whole-rock geochemistry and Hf-Pb isotopes reveal that the granite porphyry and rhyolite both originated from a mantle-derived juvenile component and assimilated by minor ancient crustal material in an extensional setting. Our study demonstrates the prospect of further exploration for two mineralization events in the hydrothermal polymetallic deposits of the central Great Xing’an Range. Full article

Samples of flotation tailings generated during the exploitation and processing of Zn–Pb–Cu–Ag ore from the Rudnik mine (Serbia) were investigated for their mineralogical, geochemical, and magnetic susceptibility properties. The flotation tailings consist of a complex mineral assemblage, including silicates, carbonates, sulfides, phosphates, sulfates, oxides, hydroxides, and native elements. Quartz, calcite, and orthoclase dominate the coarse fraction (>400 µm), accompanied by epidote, Ca-garnet, and Ca-clinopyroxene. Sulfide minerals are concentrated in finer fractions (<400 µm), with pyrite and arsenopyrite being the most abundant, followed by pyrrhotite, sphalerite, galena, and chalcopyrite. These sulfides occur as dispersed grains within a silicate–carbonate matrix. Post-depositional oxidative alteration is moderately developed, with pyrite replaced by hematite, galena by cerussite, and chalcopyrite by malachite. Geochemical analyses reveal that SiO₂ (avg. 38.98 wt%), Fe₂O₃ (avg. 23.68 wt%), Al₂O₃ (avg. 8.95 wt%), CaO (avg. 9.03 wt%) and MgO (avg. 1.50 wt%) dominate the composition. Economically significant metals include Zn (avg. 0.47 wt%), Pb (avg. 0.20 wt%), Cu (avg. 0.11 wt%), Ag (max. 19 µg/g), and Bi (max. 130 µg/g). Mass magnetic susceptibility shows a strong correlation with S (r = 0.92), Co (r = 0.90), and Bi (r = 0.87); moderate correlation with Fe₂O₃, Al₂O₃, and As; and negative correlation with Mn, TiO₂, Zn, and Pb. The ferromagnetic phase most likely originates from pyrrhotite, as well as hematite formed during pyrite alteration and goethite. Full article