Search Results (20)

This study provides a comprehensive characterization of the low-to-intermediate sulfidation (LS-to-IS) epithermal Molai Zn-Pb±(Ag,Ge) ore (Vigla-Mesovouni orebody) in Laconia, Greece, and provides insights on how such data may be employed in beneficiation flow-sheet design. Detailed mineralogical, chemical, textural, and physicochemical characterization defines a systematic transition from early refractory Ge-rich to late-stage refractory Ag-rich mineralization, including sulfides and fahlores. Germanium, although present in all sphalerite varieties (Sp-I, Sp-II, and Sp-III), is predominantly enriched in early sphalerite (Sp-I, up to 1891.60 ppm). Interestingly, Ge is also enriched in early Py-I pyrite, with content reaching up to 383 ppm. Silver is mainly concentrated in late-stage tetrahedrite Ttr-II (up to 3.60%), galena (Ga-II), and, to a lesser extent, late sphalerite (Sp-III). Liberation studies reveal effective liberation of Py-I and Sp-I, major Ge carriers, in the coarser fractions (+0.150 mm) and near complete liberation of all ore phases below 0.036 mm. Combined beneficiation via Wilfley pre-concentration and differential flotation produced up to ~35% Pb and ~65% Zn at >85% recovery for the smallest fractions (−0.036 mm). Ore characterization revealed that secondary circuits may be developed to further enhance the economic value of Molai ore (Ge from Py-I, and Ag±[Sb,As] from Ttr-II and Ag-bearing sulfosalts), which are dismissed as wastes in Pb and Zn flotation circuits. The results of our study establish a robust foundation for the design of tailored, multi-stage metallurgical flow-sheets aimed at maximizing the economic value of the Molai epithermal resource. 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

An enrichment in nickel (Ni) or platinum group elements (PGE) is seldom observed in ores of the iron oxide–copper–gold (IOCG) type. This phenomenon is, however, known from a few deposits and prospects in the Carajás Mineral Province, Brazil. The Ni-PGE enrichment is explained, in part, by the spatial association of the IOCG-type ores with altered mafic-ultramafic lithologies, as well as by reworking and remobilization of pre-existing Ni and PGE during multiple mineralization and tectonothermal events across the Archean-Proterozoic. One such example of this mineralization is the Jatobá deposit in the southern copper belt of the Carajás Domain. This is the first detailed study of the Ni and PGE mineralization at Jatobá, with implications for understanding ore genesis. Petrographic and compositional study of sulfides shows that pyrite is the main Ni carrier, followed by pyrrhotite and exsolved pentlandite. Measurable concentrations of palladium (Pd) and platinum (Pt), albeit never more than a few ppm, are noted in pyrite. More importantly, however, the trace mineral signature of the Jatobá deposit features several platinum group minerals (PGM), including merenskyite, naldrettite, sudburyite, kotulskite, sperrylite, and borovskite. These PGM occur as sub-10 µm-sized grains that are largely restricted to fractures and grain boundaries in pyrite. All Pd minerals reported contain mobile elements such as Te, Bi, and Sb and are associated with rare earth- and U-minerals. This conspicuous mineralogy, differences in sulfide chemistry between the magnetite-hosted ore and stringer mineralization without magnetite, and microstructural control point to a genetic model for the sulfide mineralization at Jatobá and its relative enrichment in Ni and PGE. Observations support two alternative scenarios for ore genesis. In the first, an initial precipitation of disseminated or semi-massive Ni-PGE-bearing sulfides took place within the mafic rock pile, possibly in a VHMS-like setting. Later partial dissolution and remobilization of this pre-existing mineralization by mineralizing fluids of IOCG-type, possibly during the retrograde stage of a syn-deformational metamorphic event, led to their re-concentration within magnetite along structural conduits. The superposition of IOCG-style mineralization onto a pre-existing assemblage resulted in the observed replacement and overprinting in which PGE combined with components of the IOCG fluids like Sb, Bi, and Te. An alternative model involves leaching, by the IOCG-type fluids, of Ni and PGE from komatiites within the sequence or from ultramafic rocks in the basement. The discovery of PGM in Jatobá emphasizes the potential for additional discoveries of Ni-PGE-enriched ores elsewhere in the Carajás Domain and in analogous settings elsewhere. Full article

Mineralization characterized by Au, Hg, and Tl enrichment is rare, and research on Au, Hg, and Tl mineralization is limited. The Lanmuchang Au–Hg–Tl deposit is located in the “Golden Triangle” of Yunnan, Guizhou, and Guangxi Provinces in China. In this study, we used scanning electron microscopy (SEM), electron microprobe analysis (EPMA), and a Tescan integrated mineral analyzer (TIMA) to analyze the mineral composition and distribution of the different types of ores and identify the occurrence state and enrichment mechanism of ore-forming elements in the Lanmuchang deposit. The results show that the primary ore minerals in the Lanmuchang deposit are pyrite, cinnabar, and lorandite. Cinnabar is the primary carrier of Hg (>90%), and pyrite is the primary carrier of Tl (>60%). Gold, Hg, and Tl primarily occur as solid solutions in hydrothermal pyrite, whereas they primarily occur as nano-scale particles in diagenetic pyrite. The substitution of As for S in hydrothermal pyrite promotes Au enrichment. The coupled substitution of 2Fe²⁺ ⇔ Tl⁺ + As³⁺ may be a significant Tl incorporation mechanism and promotes the occurrence of Hg in pyrite. The As and Se contents and Cu/Au and Co/Ni ratios of the hydrothermal pyrite demonstrate that the ore-forming fluid was mostly in a low-temperature, low-salinity, almost-neutral pH, and nearly reducing environment. The results show that the mineralization of the Lanmuchang deposit is associated with the cooling, oxidation, water–rock interaction, and boiling processes of the ore-forming fluid(s). Full article

The use of thiosulfate to extract gold from refractory ores is promising because of its non-toxicity and high selectivity. Sulfide minerals (i.e., pyrite, arsenopyrite, chalcopyrite), major gold carriers in refractory gold ores, however, hinder gold extraction due to the high consumption of a lixiviant. In this study, a new method to improve gold extraction from sulfide bearing gold ores is proposed based on the model experiments using a mixture of gold powder and arsenopyrite-bearing sulfide (HAsBS) ore. The effects of HAsBS ore on gold leaching in ammonium thiosulfate solutions were investigated, and it was found that gold extraction in the presence of HAsBS ore was suppressed because of the unwanted decomposition of thiosulfate on the surface of sulfide minerals. To improve gold extraction in the presence of the sulfide minerals, this study investigated the effects of the pretreatment of HAsBS ore using ammonium solutions containing cupric ions and confirmed that HAsBS ore was oxidized in the pretreatment and its surface was covered by the oxidation products. As a result, thiosulfate consumption was minimized in the subsequent gold leaching step using ammonium thiosulfate, resulting in an improvement in gold extraction from 10% to 79%. Full article

Carrier flotation is a technique that can recover fine particles by using coarse carrier particles during the flotation process. In heterogeneous carrier flotation, coarse mineral particles of different minerals are used as carriers to recover fine mineral particles. By using Cu²⁺-treated pyrite particles as carriers, fine chalcopyrite particles recovery could be improved. However, a disadvantage of this heterogeneous carrier flotation is that it requires a post-flotation separation process to improve the grade of the final Cu concentrate. This study tested mechanical and chemical treatments to detach finely ground chalcopyrite (D₅₀~3.5 µm) particles from Cu²⁺-treated coarse pyrite particles (−125 + 106 µm) after flotation. The results showed that the ultrasonic treatment was not effective to detach chalcopyrite fines from Cu²⁺-treated pyrite particles. However, acid treatment was effective to detach chalcopyrite fines from coarse pyrite particles. At pH 2, approximately 96% of chalcopyrite fines were detached from coarse Cu²⁺-treated pyrite particles. The acid treatment of flotation froth (mixture of chalcopyrite fines and Cu²⁺-treated pyrite particles) decomposed the collector KAX (potassium amyl xanthate) and dissolved the Cu precipitates adsorbed on the pyrite surface. This weakened the hydrophobic attraction force between the chalcopyrite fines and coarse pyrite particles, thus promoting the detachment of chalcopyrite fines from Cu²⁺-treated coarse pyrite particles. Full article

The Elatsite–Chelopech ore field in the northern part of the Panagyurishte district in Central Bulgaria comprises numerous spatially associated porphyry copper and epithermal gold deposits and prospects. In addition to the mineralization and alteration features, trace elements, lead and sulfur isotope signatures of sulfide minerals from porphyry copper, base metal and gold-base metal deposits/prospects have been studied. LA-ICP-MS analyses of pyrite, arsenopyrite and sulfosalt minerals validate them as major carriers for Au, Ag, Sb, Se and Co. Pyrite from the three types of mineralization has specific geochemical characteristics. Pyrite from the porphyry copper deposits/prospects has generally lower total trace element content compared to pyrite from the epithermal prospects, except for Se, Co and Ni. Pyrite from the base metal and gold-base metal veins is enriched in As, Au, Ag, Sb and Pb. In pyrite from the base metal deposits, Co and Ni have contents comparable to the pyrite from the porphyry copper deposits, while pyrite from the gold-base metal veins shows lower Co and Ni. Arsenopyrite from these deposits shows similar features. Similarly, sphalerite from the gold-base metal veins also has lower Co content compared to sphalerite from the base metal veins but higher In and Cu contents. In addition to the close spatial relationships between the Elatsite and Gorna Kamenitsa porphyry Cu deposits and Negarstitsa-West and Dolna Kamenitsa base metal prospects, as well as similarities in the mineralization and alteration styles, the lead isotopic (²⁰⁶Pb/²⁰⁴Pb = 18.61–18.68, ²⁰⁷Pb/²⁰⁴Pb = 15.64–15.65 for porphyry and ²⁰⁶Pb/²⁰⁴Pb = 18.55–18.67, ²⁰⁷Pb/²⁰⁴Pb = 15.64–15.68 for base metal) and sulfur isotopic (δ³⁴S values of −3 to +1‰ for porphyry and δ³⁴S values of −1.7 to +3.5‰ for base metal) signatures of sulfides support the idea of a genetic link between these two types of deposits. The porphyry and base-metal mineralization result from a common major ore-forming event during the Late Cretaceous, corresponding to deep/higher-temperature and shallower/distal/lower-temperature environments, respectively. In particular, more radiogenic lead (²⁰⁶Pb/²⁰⁴Pb = 18.41–18.47, ²⁰⁷Pb/²⁰⁴Pb = 15.67–15.76) and slightly different sulfur isotopic compositions (δ³⁴S values of +3.5 to +10.6‰) of sulfides from the distal gold-base metal veins of Kordunsko Dere, Svishti Plaz and Shipkite might be a consequence of the interaction of the ore-forming fluids with an external older crustal and isotopically positive S source. Alternatively, a different fluid source/event for the formation of these gold-base metal veins may be suggested. Full article

Sedimentary phosphate rocks are characteristically rich in organic matter, and contain sulfides and a high concentration of trace elements, including cadmium (Cd), which is harmful to the human body. The mining of phosphate rock and phosphogypsum at Qingping has expanded the release of Cd into groundwater and farmland soil. To prevent and control Cd pollution it is critical to reveal the carrier mineral phase(s) and migration mechanism of Cd and other elements in phosphate rock and phosphogypsum. The elemental and mineral composition of bulk samples were analysed by XRF, ICP-MS, and XRD, respectively. The results showed that from phosphate rock to phosphogypsum, the main constituent elements changed from CaO (49.43%) and P₂O₅ (36.63%) to CaO (33.65%) and SO₃ (>34%), and the main mineral changed from fluorapatite to gypsum. Among all the elements, the element transfer factor (ETF) of P₂O₅, F, Co, U, Cd, and other elements was low; the ETF (Cd) was only 10.85%, and only a small amount of Cd entered the acidic phosphogypsum during the production process. Raman spectroscopy analysis revealed two types of apatite: the brown–black apatite with organic matter (type 1) and the yellow–light brown apatite without organic matter (type 2). LA-ICP-MS analysis showed that the Cd element content in type 2 was lower, while the organic matter and Cd element content in type 1 were higher, suggesting that Cd may be controlled by organic matter, and the relationship with apatite is not apparent. Electron probe analysis and XRD semiquantitative results show that the content of Cd in pyrite is higher (511 ppm), which is significantly higher than that of bulk rock. In addition, pyrite is rich in Co, As, Ni, Zn, and other elements. The content of Cd in phosphate ore shows a good correlation with that of pyrite. Cd in Qingping phosphate rock is mainly controlled by organic matter and pyrite, and only a small amount of Cd is transferred to phosphogypsum. Reducing the environment leads to the enrichment of Cd in phosphate rock. Full article

Both complete and uncompleted radiolarian siliceous shells were developed at Wufeng-Longmaxi radiolarian siliceous shale laminae in Sichuan Basin. Micro- and ultra-micropetrological observation suggests that they were successively filled by calcite, pyrite and organic–silicon complex, where pyrite and organic–silicon complex filled dissolved pores associated with calcite during sedimentation. Calcite was derived from calcium carbonate produced by microbial activities at the seawater surface. The environment of radiolarian siliceous shell cavities, which was suitable for sulfate reducing bacterial growth or dissolved hydrogen sulfide reducing Fe³⁺, contributed positively to pyrite development. Organic–silicon complex development was related to microorganism metabolism that was an important silica source. Honeycomb-like organic pores were developed in cavities with complete shells, but were not developed in cavities with uncompleted shells. This is because the latter could not withstand overburden pressure compared with the former. The only approach to figure out organic pore carriers and understand sequences and development processes of minerals and organic matter is to select weakly compacted radiolarian siliceous shale laminae to carry out micro- and ultra-micropetrological observation and geochemical testing via various technologies. Full article

The potential environmental impact of historical mining and ore processing on stream sediments and water was studied in a small siderite iron ore deposit with diverse sulfide mineral paragenesis. The main aim was to characterize solid carriers of potentially toxic elements (PTEs) in stream sediments and mine waste, to understand their fate in fluvial systems. General mineralogy (X-ray powder diffraction) and individual solid PTE carriers (scanning electron microscopy/energy dispersive spectroscopy) were correlated with the geochemical composition of stream sediments, mine waste, and stream waters (inductively coupled plasma mass spectrometry). Primary solid PTE carriers were pyrite, chalcopyrite, sphalerite, Hg-bearing sphalerite, galena, and siderite. Slightly alkaline and oxidizing conditions in stream water promoted the transformation of primary phases into secondary PTE carriers. Fe(Mn)-oxide/oxyhydroxides were major sinks for Pb, Zn, and As. Compared to background levels, Co (14.6 ± 2.1 mg/kg), Cu (30 ± 2.9 mg/kg), Ni (32.1 ± 2.9 mg/kg), Pb (64.5 ± 16.4 mg/kg), Zn (175.3 ± 22.5 mg/kg), As (81.1 ± 63.7 mg/kg), and Hg (2 ± 0.8 mg/kg) were elevated in mining area. Mine waste contained similar PTE carriers as stream sediments, but much higher PTE contents. Prevailingly low PTE concentrations in streams, with the exception of As (1.97 ± 2.4 µg/L) and Zn (4.5 ± 5.7 µg/L), indicate the stability of PTE carriers. Environmental effects were not significant, and additional monitoring is recommended. Full article

Intimate knowledge of the mineralogical assembly of the Yushui complex ore rich in Cu, Pb, and Ag is essential if efficient separation processing is to be conducted. With the aid of testing instruments, such as scanning electron microscope (SEM), X-ray diffractometer (XRD), and mineral liberation analyzer (MLA) combined with energy-dispersive X-ray analysis (EDX), the texture, such as the size distribution, dissemination, and association of the minerals, was investigated. The results demonstrate that the ore consists of 35 categories of minerals, assaying Cu 7.99%, Pb 9.39%, and Zn 1.96% in the forms of chalcopyrite, galena, and sphalerite, respectively, and silver assaying 157.9 g/t is closely associated with these sulfides; sulfides are present in amounts of 80.31% of the total, traditional gangues only 19.69%, and pyrite as a Cu-Pb-Zn-Ag carrier mineral up to 44.80%. According to the characteristics of the ore, the innovative process of flash copper flotation in weak acidic pulp and lead flotation, followed by further copper recovery, was developed. The closed-circuit test shows that copper concentrate assays Cu 16.33%, Pb 7.98%, Ag 242 g/t at Cu recovery of 86.67%; lead concentrate contains Pb 46.23%, Cu 3.75%, Ag 165 g/t at Pb recovery of 56.84%; total recovery of silver in both concentrates is 75.57%. Full article

On the basis of geochemical whole-rock and mineralogical point analyses, the concentrations of V and Co were determined in magnetite-ilmenite oxide ores, associated with sulphides, at the Krzemianka and Udryn deposits in the Mesoproterozoic Suwałki Anorthosite Massif (SAM) in NE Poland. EPMA analyses showed that the main carrier of vanadium was magnetite (mean = 0.42 wt%) and, to a lesser extent, ilmenite (mean = 0.14 wt%) and minor Al-spinels (mean = 0.04 wt%). In turn, cobalt was found mainly in the form of isomorphic substitutions in magmatic sulphides such as pentlandite (mean = 4.41 wt% Co), pyrrhotite (mean = 0.16 wt%), and chalcopyrite (mean = 0.11 wt%). Moreover, Co-enrichments were also recognized in the secondary sulphides, such as pyrite and bravoite, replacing pyrrhotite (means = 1.6 and 2.7 wt% Co, respectively), and in the form of different thiospinels ((Fe, Ni) (Co, Ni)₂S₄), mainly siegenite (mean = 22.0 wt% Co), replacing pyrrhotite and pentlandite. Vanadium cations were substituted in Fe, Ti oxide minerals in place of Fe⁺³ cations, and in the case of cobalt, Fe⁺² cations were substituted in sulphides and thiospinels. Vanadium and cobalt showed high Person’s correlation coefficients (r = 0.70), indicating their close spatial coexistence and a common source, which was parental anorthosite-norite magma of the SAM suites. The common magma genesis of magnetite-ilmenite and sulphide mineralization was also confirmed by the very similar shapes of the curves of REE content in the oxide-sulphide ores in relation to chondrite, in which negative Eu anomalies and positive Sm anomalies are clearly visible. Although the average contents of vanadium and cobalt were low (arithmetic means = 960 ppm, and 122 ppm, respectively), the resources of these metals were estimated to be large due to the enormous reserves of magnetite-ilmenite ores hosted by the SAM. However, the Fe-Ti-V ores associated with Fe, Ni, Co, and Cu sulphides were considered to be sub-economic because of their depth of occurrence (mainly 1.0 km below the surface level); their metal contents, which were usually too low; and additionally the fact that the location is in a highly environmentally protected landscape and lake area. Full article

Widespread hexavalent chromium (Cr (VI)) in the environment has become a worldwide problem, and economical and efficient treatment is urgently needed. In this paper, the treatment method of Cr (VI) by microorganisms and iron minerals (pyrite and magnetite) under anaerobic conditions was investigated. Furthermore, the influence of Cr (VI) on the microbial community structure was explored. The reduction test demonstrated that the removal rate of Cr (VI) in a single biological group was 54.96%; however, in the pyrite and biological groups and magnetite and biological groups, the removal rates of Cr (VI) increased to 83.06% and 78.23%, respectively. Microorganisms and iron minerals work together to produce a better removal effect on the removal rate of Cr (VI). Mechanistic studies have found that in the process of Cr (VI) reduction, a passivation layer is formed on the surface of the mineral that hinders the progress of the reaction. The addition of bacteria can reduce the negative impact of the passivation layer. At the same time, iron minerals have better electron-receiving and -conducting ability and can be used as electron carriers for bacteria to reduce Cr (VI). In addition, iron minerals and the disappearance of Cr (VI) will change the structure of the community and affect the expression of its functions, which is more conducive to reducing Cr (VI). This work sheds new light on the treatment of heavy metal pollution and the understanding of the synergistic reduction mechanism of Cr (VI). Full article

This paper provides new geochemical data focusing on valuable elements in the coal, parting, and floor samples in the No. 5 coal seam of the Taiyuan Formation from the Wujiawan mine, Datong coalfield, northern China. The minerals mainly consist of kaolinite, calcite, and pyrite, as well as trace amounts of quartz and illite. The No. 5 coal is enriched in Li, Ga, high field strength elements (HFSEs), and rare earth elements and yttrium (REY) when compared with world hard coals. Of particular interest is the high average concentration of Li (67.66 μg/g), which is around seven times higher than the value for world hard coals. Lithium, Ga, and HFSEs have strong inorganic affinities, whereas REY have organic affinities. The main carrier of Li, Ga, and HFSEs is aluminosilicate minerals, while REY appear to occur with organophosphorus. These HFSEs are enriched, both in the parting and in the adjacent coal samples. This suggests that these elements are likely to leach out during the diagenetic process. The distribution patterns of REY, along with the ratio of Al₂O₃/TiO₂ and the figure of Zr/TiO₂ vs. Nb/Y are suggestive of their derivation from felsic parent material. In the northern and eastern part of the Datong coalfield, there are several regions where the Li content is higher than the mineable grade, in particular in the northern Datong coalfield where there is a mine with an Li content of 294.6 μg/g. This is significantly higher than the mineable grade. Therefore, there is a potential for financially viable recovery of Li in these coals of the Datong coalfield. Full article

The trace element (TS) composition of isocubanite, chalcopyrite, pyrite, bornite, and covellite from oxidized Cu-rich massive sulfides of the Ashadze-2 hydrothermal field (12°58′ N, Mid-Atlantic Ridge) is studied using LA-ICP-MS. The understanding of TE behavior, which depends on the formation conditions and the mode of TE occurrence, in sulfides is important, since they are potential sources for byproduct TEs. Isocubanite has the highest Co contents). Chalcopyrite concentrates most Au. Bornite has the highest amounts of Se, Sn, and Te. Crystalline pyrite is a main carrier of Mn. Covellite after isocubanite is a host to the highest Sr, Ag, and Bi contents. Covellite after pyrite accumulates V, Ga and In. The isocubanite+chalcopyrite aggregates in altered gabrro contain the highest amounts of Ni, Zn, As, Mo, Cd, Sb (166 ppm), Tl, and Pb. The trace element geochemistry of sulfides is mainly controlled by local formation conditions. Submarine oxidation results in the formation of covellite and its enrichment in most trace elements relative to primary sulfides. This is a result of incorporation of seawater-derived elements and seawater-affected dissolution of accessory minerals (native gold, galena and clausthalite). Full article