Search Results (12)

The Bailugou vein-type zinc-lead-silver deposit is located in the Eastern Qinling Orogen, China. There has been a long-standing debate about whether its formation is related to magmatism or metamorphism. To determine the origin of ore-forming materials and fluids, we conducted a geological and fluid inclusion investigation of the Bailugou. Field surveys show that the vein-type orebodies are controlled by faults in the dolomitic marbles of the Mesoproterozoic Guandaokou Group, and they are distal to the regional Yanshanian intrusions. Four ore stages, i.e., quartz–pyrite ± sphalerite (Stage 1), quartz–polymetallic sulfides (Stage 2), dolomite–polymetallic sulfides (Stage 3), and calcite (Stage 4), are identified through microscopic observation. The homogenization temperatures of measured fluid inclusions vary in the range of 100 °C to 400 °C, with the dominating concentration at 350 °C to 400 °C, displaying a descending trend from early to late stages. The estimated formation depth of the Bailugou deposit varies from 2 km to 12 km, which is deeper than the metallogenic limit of the epithermal hydrothermal deposit but conforms to the typical characteristics of a fault-controlled deposit. The ore-forming fluid in Stage 1 originates from a fluid mixture and experiences a phase separation (or fluid immiscibility) between the metamorphic-sourced fluid and the fluids associated with ore-bearing carbonate-shale-chert association (CSC) strata. This process results in the transition to metamorphic hydrothermal fluid due to water–rock interactions in Stage 2, culminating in gradual weakening and potential fluid boiling during the mineralization of Stage 3. Collectively, the Bailugou lead-zinc-silver mineralization resembles an orogenic-type deposit formed by metamorphic fluids in the Qinling Yanshanian intracontinental orogeny. Full article

The manganese deposits at the Kato Nevrokopi area are located in the Drama Basin (Northern Greece) and belong to the Rhodope Metamorphic Province. The deposits were previously exploited for several supergene Mn-oxide ore bodies of massive, battery-grade nsutite, spatially associated with fault zones in the vicinity of Oligocene granitic intrusions. We conducted detailed geological, mineralogical, and geochemical investigations at the Mavro Xylo deposit, which led to the identification of Ag-rich Mn-Zn±Pb vein-type mineralization. The studied paragenesis appears to have developed during two hydrothermal stages: stage I, characterized by the mineral assemblage rhodonite–quartz–rhodochrosite–pyrophanite–pyrite–galena–Te bearing argentite–sphalerite–wurtzite–alabandite, and stage II, dominated by Ag-rich, Mn-Zn±Pb oxides in the form of fracture-fills along a high-angle NE-SW fault zone in brecciated marbles. Bulk analyses of the stage-II oxide assemblage yielded concentrations of Ag up to 0.57 wt.%. In the veins, wurtzite is present in bands, succeeded by manganese oxides, while calcite and quartz are the main gangue minerals. We placed particular emphasis on the occurrence of Ag in high concentrations within distinct manganese oxides. Major silver carriers include Zn-bearing todorokite, chalcophanite, and hydrous Pb-Mn oxide. The vein-type mineralization at Mavro Xylo shares many characteristics with other intermediate-sulfidation epithermal precious metal-rich deposits associated with high Mn concentrations. The evolution of the mineral paragenesis indicates a change in the physicochemical attributes of the ore-forming fluids, from initially reducing (stage I) to oxidizing (stage II). Although the origin of the initial ore-forming fluid remains to be constrained, the above redox change is tentatively attributed to the increasing incursion of meteoric waters over time. Full article

The supergiant Shuangjianzishan (SJS) Ag–Pb–Zn deposit, located in the southern Great Xing’an Range (SGXR), is the largest Ag deposit in China. The SJS deposit can be divided into two ore blocks: the Shuangjianzishan ore block and the Xinglongshan ore block. Given the importance of the Xinglongshan ore block in the SJS deposit, our work is focused on the Xinglongshan ore block. The vein orebodies in the Xionglongshan ore block mainly occur in the NW-, NNW-, and NNE-trending fault zones, and its mineralization is mainly related to a deep concealed syenogranite. Here, we present new geochronology, isotope geochemistry, and fluid inclusion data for the Xinglongshan ore block and provide additional insights into the metallogenic mechanism of the deposit. The dating results show that the syenogranite related to the mineralization formed at approximately 137 Ma, which is coherent with some previous age determinations in sulfides from the ore deposit. The mineralization of the Xinglongshan ore block can be divided into four stages: sphalerite–arsenopyrite–pyrite–chalcopyrite–quartz stage (stage I), sphalerite–galena–pyrite–silver-bearing mineral–quartz stage (stage II), sphalerite–galena–silver-bearing mineral–quartz–calcite stage (stage III), and weakly mineralized quartz–calcite stage (stage IV). Four types of fluid inclusions (FIs) have been identified within quartz and calcite veins: liquid-rich, gas-rich, pure-liquid, and pure-gas FIs. The homogenization temperatures in the four stages exhibit a gradual decrease, with stage I ranging from 253 to 302 °C, stage II from 203 to 268 °C, stage III from 184 to 222 °C, and stage IV from 153 to 198 °C, respectively. The salinity for stages I, II, III, and IV falls within the ranges of 3.4–6.6 wt% NaCl eqv., 2.6–7.2 wt% NaCl eqv., 2.9–7.0 wt% NaCl eqv., and 1.2–4.8 wt% NaCl eqv., respectively, indicative of a low-salinity ore-forming fluid. The δ¹⁸O_water and δD values of the ore-forming fluid span from −13.9‰ to 7.4‰ and −145‰ to −65‰, with δ¹³C_V-PDB values between −11.0‰ and −7.9‰. These values suggest that the ore-forming fluid predominantly originated from a mixture of magmatic and meteoric water. The ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb, and ²⁰⁸Pb/²⁰⁴Pb ratios of sulfides range from 18.278 to 18.361, 15.530 to 15.634, and 38.107 to 38.448, respectively. These ratios imply that the ore-forming material was primarily derived from the Early Cretaceous granitic magma, which resulted from the mixing of depleted mantle- and crustal-derived magmas. The fluid mixing was the dominant mechanism for mineral precipitation. The Xinglongshan ore block belongs to a magmatic-hydrothermal vein-type deposit related to the Early Cretaceous syenogranite, and the Shuangjianzishan ore block belongs to an intermediate sulfidation epithermal deposit related to coeval subvolcanic rocks. The Ag–Pb–Zn mineralization at Shuangjianzishan is genetically related to the Early Cretaceous volcanic–intrusive complex. Full article

The Niuxingba-Liumukeng deposit, located in the Yinkeng ore field (Jiangxi province, South China), is a typical Ag-Pb-Zn deposit hosted in the Yudu-Ganxian metallogenic belt. Based on the field investigation and mineralogical studies, the mineralization of this deposit can be divided into three stages: quartz-pyrite-arsenopyrite stage (I), quartz-galena-sphalerite-sulfosalt stage (II), and quartz-carbonate stage (III), with stage II being the main Ag mineralization stage. In this contribution, we reported the occurrence of bismuth-bearing minerals in this hydrothermal deposit and its implications for ore formation. Based on the results of electron microprobe analyses, we infer that the dominant occurrence of bismuth at Niuxingba-Liumukeng is primarily marked by solid solutions within the crystal lattice of galena and as visible independent bismuth-bearing minerals. The independent bismuth minerals consist of berryite [Pb₃(Ag,Cu)₅Bi₇S₁₆], emplectite (CuBiS₂), and aikinite (PbCuBiS₃). Most bismuth minerals replace chalcopyrite or fill in the cracks of pyrite and chalcopyrite. Meanwhile, we found a large number of Bi-bearing minerals closely coexisting with Ag-bearing minerals, indicating that bismuth may have played a crucial role in silver deposition from hydrothermal fluids. We considered that the existence of bismuth-rich melts associated with the ore-forming hydrothermal systems could help to promote the enrichment and precipitation of silver to form economic ores. Full article

Various magmatic–hydrothermal activities have resulted in different styles of polymetallic mineralization in South China. Shuikoushan is a large Fe-Cu-Pb-Zn-Au-Ag orefield situated in fold-and-thrust belts within the South China Block. Two types of granodiorite have been identified in recent drilling work. The early-stage, coarse-grained granodiorite has developed magnetite-bearing skarns in the deep level. The late-stage, fine-grained granodiorite is associated with garnet-hematite–magnetite–pyrite–sphalerite–chalcopyrite-bearing skarns in its contact zone. Away from the garnet-bearing skarn are calcite–quartz–pyrite–sphalerite–galena veinlets in faulted breccia. Fieldwork has identified iron mineralization in both skarns, whereas copper mineralization was only discovered in the garnet-bearing skarns. Lead, zinc, gold, and silver mineralization were observed in the garnet-bearing skarns and faulted breccia. Zircon U–Pb analyses suggested the emplacement of two granodiorite at 167.8 ± 0.8 Ma (MSWD = 1.1, N = 31) and 163.6 ± 0.7 Ma (MSWD = 1.3, N = 32). Apatite and garnet U–Pb dating further indicated the magnetite-bearing skarns of 166.2 ± 1.9 Ma (MSWD = 4.5, N = 27), the hematite–magnetite–sulfide-bearing skarns of 158.6 ± 2.8 Ma (MSWD = 1.3, N = 34), and the calcite–quartz–sulfide veinlets of 159.5 ± 5.2 Ma (MSWD = 1.7, N = 24). The time–space relationship between the two intrusions and hydrothermal activities suggests that the fine-grained granodiorite is responsible for polymetallic mineralization. Whole-rock geochemistry analyses demonstrated the enrichment of LILEs and the depletion of Nb and Ta in two granodiorites, with a slight enrichment in LREEs and flat HREE patterns. These granodiorite bodies therefore belong to high-K calc-alkaline magma generated via the crust’s partial melting. The fine-grained granodiorite generally has a lower HREE and higher Dy/Yb, Sr/Y ratios than coarse-grained granodiorite, corresponding to the source of magma in garnet stable lower crust. The residual garnet keeps ferric iron in melts, leaving the fine-granodiorite more oxidized for copper and gold concentration. Through these analyses and our drilling work, a continuous skarn–hydrothermal–epithermal system has been identified for Cu-Pb-Zn-Au-Ag targeting in Shuikoushan. Full article

In this work, bio-hydrometallurgy technology was employed and a novel two-stage method based on successive chemical and bio treatments was proposed to collaboratively utilize manganese–silver ore and silver-bearing pyrite. In the optimization research of the chemical leaching stage, the sensitive factors for the Mn leaching efficiency were screened by Plackett–Burman design, and central compound design was performed to settle the optimized parameters. A mixed strain of bacteria containing Sulfobacillus thermosulfidooxidans, At. caldus and Leptospirillum ferrooxidans was applied in the bioleaching stage. A conventional cyanidation process carried out with the Mn leaching residuals suggested an efficient recovery of Ag. Applying a two-stage method with the optimum conditions, the leaching efficiency of 95.3% (Mn) and 96.3% (Ag) were obtained with 284.94 kg/t silver-bearing pyrite addition and 277.44 kg/t sulfuric acid consumption with a temperature at 77.73 °C and stirring speed at 287.76 rpm. Mineral behaviors were investigated with XRD and SEM/EDS analysis, and it was revealed that the oxidation of sulfur is the crux in reducing the usage of reagents, and the presence of leaching bacteria enhanced the oxidation efficiently. Through optimization and mechanism study, this paper provides an opportunity to co-leach the manganese–silver ore and silver-bearing pyrite process in a more economical and environmental way. Full article

The aim of this study was to characterize historical slags which originated during silver production from the Jihlava ore district, Czech Republic. The area was among the head producers of silver within the Lands of the Czech Crown in 13th–14th centuries. The mined ores had complex composition, being formed mostly by pyrite, sphalerite, galena, chalcopyrite, and accessory silver-rich minerals such as silver-bearing tetrahedrite (freibergite) or pyrargyrite, with gangue represented by quartz and Mn-rich carbonates or baryte. Large volumes of slags with contrasting composition were generated during the Pb-Ag production. Altogether, two main types of slags were identified in the district. The first type is characterized by high BaO contents (up to 34.5 wt.%) and dominancy of glass, minor quartz, and accessory amounts of Ba-rich feldspar (up to 93 mol.% of Cls), metal-rich inclusions, Ba-Pb sulphates and only rare pyroxene, wollastonite and melilite. The composition of the second group belongs to fayalitic slags containing glass, Fe-rich olivine, accessory pyroxene, feldspar, quartz, and inclusions of various metallic phases. Fluxes were derived from gangue (quartz, carbonates, baryte) or local host rocks for both types of slag. The calculated viscosity indexes reflect (with minor exceptions) medium-to-high effectivity of metal separation. Smelting temperatures were estimated from a series of ternary plots; however, more reliable estimates for both types of slags were obtained only from experimental determination of melting temperature and calculations using bulk/glass compositions (~1100–1200 °C). Full article

Eunjeok Au–Ag deposits are situated in the Yeongam district, Cheollanamdo-province, South Korea. They are genetically related to the Bulgugsa magmatic event (ca. 110–60 Ma), caused by the transition in the subduction direction and style of the Izanagi Plate. Three gold- and silver-bearing hydrothermal veins filled the fractures of the Cretaceous rhyolitic tuff. The major ore minerals were arsenopyrite (31.47–32.20 at.% As), pyrite, chalcopyrite, sphalerite (8.58–10.71 FeS mole%) and galena with minor amounts of electrum (62.77–78.15 at.% Au), native silver, and argentite. Sericitization was dominant in the alteration zone. The various textures of quartz veins (i.e., breccia, crustiform, comb, and vuggy) may indicate the formation of an epithermal environment. The auriferous fluids with the H₂O–NaCl system have homogenization temperatures and salinities of 204 °C to 314 °C, less than 10 wt.% equiv. NaCl, and experienced mixing (dilution and cooling) events during mineralization. Considering the characteristics of the geologic setting, major fault system, and host rock, the Eunjeok Au–Ag deposit within the Yeongam district tends to share the general geologic characteristics of Haenam–Jindo epithermal mineralization episodes. However, the age of gold–silver mineralization (86.0 Ma) is older than that of Haenam–Jindo epithermal mineralization episodes (<70.3 Ma), implying some differences exist in the genetic sequence of extensional characteristics caused by transcurrent Gwangju–Yeongdong faults. Full article

The Igoudrane mine with a total production of 700,000 t of ore grading 485 g/t Ag is currently one of the most productive mines in the Imiter district of the eastern Anti-Atlas in Morocco. The silver-rich ± base metal deposit occurs dominantly as vein- and hydrothermal breccia-hosted orebodies at the interface between the lower Ediacaran turbidites of the Saghro Group and the unconformably overlying, dominantly felsic volcanic, and volcaniclastic rocks of the late Ediacaran Ouarzazate Group. Higher-grade ores are lithologically hosted by the uppermost organic-rich black shale unit and structurally controlled by the intersection of subvertical NW- and NE-trending fault systems. Ore-related hydrothermal alteration includes, in order of decreasing abundance, carbonatization, silicification, sericitization, and chloritization. Three primary paragenetic stages of veining and associated silver ± base metal mineralization have been recognized: (1) early pyrite + quartz + Ag-bearing sulfides and sulfosalts; (2) main Ag-bearing sulfides and sulfosalts + calcite ± fluorite ± dolomite; and (3) late quartz + calcite + base-metal sulfides (galena, sphalerite, pyrite, chalcopyrite). Irrespective of the ore stage, the dominant Ag-bearing ore minerals are Ag-Hg amalgam, argentite, freibergite, acanthite, polybasite, pyrargyrite, and proustite. Fluid inclusion data show a trend of decreasing temperatures with time, from the main silver stage (T_h = 180 ± 12 °C) to late base-metal stage (T_h = 146 ± 7 °C), consistent with fluid mixing, cooling, and/or dilution. The coexistence of aqueous-rich and vapor-rich fluid inclusions together with variations in bulk salinity (NaCl + CaCl₂) of the mineralizing fluids during the main silver stage, at similar temperatures, indicate that boiling and subsequent degassing occurred during the main ore-forming event due to a pressure decrease. Calculated δ¹⁸O_fluid values along with REE+Y and Sr isotope constraints suggest that the ore-forming fluids originated from a predominantly magmatic source, although incursion of meteoric waters during collapse of the hydrothermal system could have contributed to deposition. The post-ore, base-metal quartz-carbonate-dominated mineralization was deposited from dilute Ca-Na-Cl-bearing fluids at temperature below 150 °C. Overall, fluid–rock interaction with the black shales along major faults and thin permeable horizons, boiling-degassing—with subsequent fluid mixing, cooling, and/or dilution—were the main mechanisms of silver deposition. Full article

A significant part of the primary gold reserves in the world is contained in sulphide ores, many types of which are refractory in gold processing. The deposits of refractory sulphide ores will be the main potential source of gold production in the future. The refractory gold and silver in sulphide ores can be associated with micro- and nano-sized inclusions of Au and Ag minerals as well as isomorphous, adsorbed and other species of noble metals (NM) not thoroughly investigated. For gold and gold-bearing deposits of the Urals, distribution and forms of NM were studied in base metal sulphides by laser ablation-inductively coupled plasma mass spectrometry and by neutron activation analysis. Composition of arsenopyrite and As-pyrite, proper Au and Ag minerals were identified using electron probe microanalysis. The ratio of various forms of invisible gold—which includes nanoparticles and chemically bound gold—in sulphides is discussed. Observations were also performed on about 120 synthetic crystals of NM-doped sphalerite and greenockite. In VMS ores with increasing metamorphism, C_Au and C_Ag in the major sulphides (sphalerite, chalcopyrite, pyrite) generally decrease. A portion of invisible gold also decreases —from ~65–85% to ~35–60% of the total Au. As a result of recrystallisation of ores, the invisible gold is enlarged and passes into the visible state as native gold, Au-Ag tellurides and sulphides. In the gold deposits of the Urals, the portion of invisible gold is usually <30% of the bulk Au. Full article

The Shanmen Ag deposit, located in the southeastern part of the Siping area, Jilin Province, is one of the large-scale Ag deposits in Northeastern (NE) China. Almost all Ag orebodies, Ag-bearing quartz-sulfide veins are strictly controlled by NE-trending faults or brittle fractures and are hosted in the Yanshanian monzonite and quartz diorite. In terms of deposit geology, three mineralization stages are recognized: the pyrite-quartz stage (I), the quartz-Ag-polymetallic sulfide stage (II), and the carbonate-quartz stage (III). The research results of the fluid inclusions in the different stages indicate that the early stage (Stage I) mainly contains three types of fluid inclusions: liquid-rich two-phase (L-type), vapor-rich two-phase (V-type), and CO₂ aqueous multi-phase (C-type). The fluid belongs to a medium–high temperature and medium–low salinity H₂O-NaCl-CO₂ system and has boiling characteristics. The middle stage (Stage II) is mainly characterized by liquid-rich two-phase (L-type) and vapor-rich two-phase (V-type) inclusions, in which the mixing of fluids of different nature leads to the escape of CO₂. Only liquid-rich two-phase (L-type) inclusions are distinguished in the late stage (Stage III). The fluids of two later stages belong to the medium-low-temperature and low-salinity H₂O-NaCl system. Homogenization temperatures from the early to late stages range from 272.2 to 412.5 °C, 124.1 to 313.3 °C, and 128.6 to 224 °C, respectively. Fluid salinities in the early to late stages range from 1.6 to 12.1, 1.4 to 8.9, and 0.4 to 5.8 wt.% NaCl equivalent, respectively. The gradually decreasing trends of homogenization temperatures and salinities and the reduction in the CO₂ content indicate that the release of CO₂ and the low-temperature environment are important causes of the precipitation of Ag-bearing minerals. The δ¹⁸O_H2O values of the ore-bearing quartz veins in the different stages range from −3.7 to +8.1‰, and the δD values of fluid inclusions in the quartz range from −113 to −103‰, indicating that the initial ore-forming fluid was mainly derived from magma and that the input of meteoric water gradually increased during the mineralization process. The δ³⁴S values (ranging from −11.4‰ to +1.8‰) and Pb isotope compositions (²⁰⁶Pb/²⁰⁴Pb = 18.143–18.189, ²⁰⁷Pb/²⁰⁴Pb = 15.543–15.599, ²⁰⁸Pb/²⁰⁴Pb = 38.062–38.251) of sulfides suggest that the ore-forming materials have mixed mantle and crustal sources. Therefore, we propose that the release of CO₂ and the low-temperature environment are important conditions for silver minerals precipitation, and the mixing of fluids of different nature is the dominant mechanism causing precipitation. The Shanmen Ag deposit can be classified as an intrusion-related medium–low temperature hydrothermal vein-type deposit. Full article

The need to explore more complex and low-grade silver ores and to develop novel and cost-effective processes to recover silver from waste is becoming an important challenge. This paper aims to characterize old, low-grade, silver tailings generated by the former Zgounder silver mine, located in Morocco. Understanding the mineralogical composition, particularly the silver deportment, was critical to allow the recovery of silver from these tailings. More than 88 samples of low grade tailings were sampled and characterized using chemical and mineralogical techniques. Froth flotation was used to recover silver bearing minerals using a combination of different collectors (dithiophosphate, dialkyl dithiophosphinates, Aero 7518, Aero 7640, alkyl dithiophosphates and potassium butyl-xanthate). The main goal was to optimize the flotation process at a laboratory scale through the testing of different parameters, such as collectors and frother types and dosage, activators and sulphidizing agents, and pH conditions. The characterization results showed that silver content varied between 30 and 440 ppm with an overall average content of 148 ppm. Silver occurs mainly in the form of native silver as well as in association with sulphides, such as acanthite and pyrite. Minor amounts of sphalerite, chalcopyrite, arsenopyrite, and hematite were identified. The flotation results showed the following optimum conditions: particle size of 63 µm, conditioning pH of 8.5, a combination of butyl-xanthate and dithiophosphate as collectors at a dosage of 80 g/t each, a concentration of 200 g/t of the activating agent (CuSO₄), 30 g/t of methyl isobutyl carbonyl (MIBC) frother and a duration time of 8 min with slow kinetics. With these optimal conditions, it was possible to achieve a maximum silver recovery yield of 84% with 1745 ppm Ag grade to be cyanided. Moreover, the environmental behavior of the final clean tailings was demonstrated to be inert using Toxicity characteristic leaching procedure (TCLP) leaching tests. Full article