Search Results (426)

Polymetallic enrichment layers are commonly found at the base of the Lower Cambrian and extensively distributed across the Upper Yangtze Platform, yet their genetic models remain controversial. This study systematically collected samples from a typical section in the southeastern Chongqing region for mineral, organic, and inorganic analyses. It investigates the relationship between the abundance of various trace metal elements and organic matter at the base of the Niutitang Formation, as well as the vertical distribution characteristics of organic carbon isotopes and organic matter features. The results indicate that the Niutitang Formation shale exhibits a distinct three-part structure from bottom to top. Various metal elements are enriched in the lower interval, showing a close correlation between the abundance of polymetallic elements and the carbon isotopes of shale organic matter. The middle interval contains the highest TOC value and the lowest Ti/Al ratio, while the upper interval shows a significant decrease in organic matter abundance, with a clear positive correlation between the excess silicon content and Ti/Al ratio. Additionally, the mixing effect of deep-sea upwelling is the primary control on the formation of polymetallic enrichment layers in the lower interval, followed by the adsorption of organic matter under anoxic conditions. The sedimentary environment of the upper interval of the Niutitang Formation trends toward oxidation, with paleoclimate shifting toward colder and drier conditions, exhibiting aeolian sedimentary features that are unfavorable for the enrichment of trace metal elements. Consequently, upwelling is a key factor in the enrichment and mineralization of trace metal elements at the base of the Lower Cambrian in the Upper Yangtze region. Full article

Mining in the Russian Far East has been developing for more than 100 years, resulting in the formation of mining technogenic systems that negatively affect all components of the environment. The purpose of this paper is to develop and present an ecological and geochemical model of supergene processes in tinsulfide and polymetallic ore mining systems. This paper presents, for the first time, the results of long-term field observations (more than 50 years): studies of numerous secondary minerals (more than 80) identified in mine workings and tailings, their natural associations, as well as the sequence, zonality, and stages of mineral formation as well as the characteristics of hydrochemical samples of river waters, contaminated by acid mine drainage (30 years of observations). Experimental modeling of sulfide oxidation was carried out under laboratory conditions (electrochemical method) and using Selektor software, which made it possible to study the process of acid mine drainage formation and to show the metal ions and ionic complexes composition, to establish Eh-pH parameters of crystallization for 52 secondary minerals, associations of primary and secondary minerals. The influence of water components on the formation of slurry and drainage in different time periods (dry, heavy rainfall, and snowmelt) is shown, and their mixing at the geochemical barrier “acid mine drainage—surface natural waters” is described. Experimental results are verified with numerous in-situ observations and mineralogical studies. The work allowed for the presentation of an environmental–geochemical model of ecosphere pollution, which describes not only the negative impact of sulfide-bearing systems of Russian Far East mining districts but locations all over the world. Full article

To explore the potential of plant trace elements as indicators in the search for concealed deposits within the W–Sn polymetallic mining area of Shizhuyuan, Hunan Province, this study focused on the geochemical characterization of 21 trace elements, including Ag, As, B, Bi, Cd, Mo, Ni, Pb, and U, in the stem and leaf tissues of three predominant plants in the area. A total of 126 plant samples were collected, covering an area of about 10 km², and analyzed using ICP-MS. The best indicator plants and sampling sites were selected using multiple indicators, including the biological absorption coefficient (X_BAC), the enrichment coefficient (K_NJ), and the contrast coefficient (K_CD). The results showed that plant leaf tissues represent the most effective sampling components for phyto-geochemical surveys in this region. Dicranopteris dichotoma exhibited markedly pronounced geochemical anomalies of Ag (0.137 µg/g), As (86.12 µg/g), Mo (0.963 µg/g), Pb (15.4 µg/g), Sb (2.03 µg/g), and Se (0.547 µg/g) and demonstrated superior absorption capabilities for Ni, Sn, Sb, Pb, and Bi in the soil, with X_BAC values of 12.0, 54.2, 23.3, 2.9, and 83.9, respectively. R-type cluster analysis and factor analysis identified four distinct mineralization element combinations: (1) Sn–As, (2) Ag–Cu–Mo, (3) Pb, and (4) Bi–Sb–Se. Consequently, D. dichotoma is a viable indicator plant for the phyto-geochemical detection of concealed Ag, Bi, Mo, Pb, Sb, Se, and Sn mineralization in mining areas. The results demonstrate that using phyto-geochemical methods for mineral prospecting is feasible and has significant application value in the Shizhuyuan mining area, which is characterized by dense vegetation and complex geological conditions. Full article

The Southern Hunan area is located in the superposition of the Qin-Hang Cu-Pb-Zn polymetallic ore belt and the Nanling W-Sn-Mo polymetallic ore belt, which is an important window to study the mineralization of W-Sn-Mo and Cu-Pb-Zn polymetallic deposits. The Baoshan deposit is a large Cu-Pb-Zn polymetallic deposit in Southern Hunan Province with obvious zones of Cu mineralization and Pb-Zn mineralization: the central part of the Baoshan deposit demonstrates contact metasomatic (skarn) Cu mineralization, while the western, northern and eastern parts demonstrate hydrothermal vein Pb-Zn mineralization. However, the origin and evolution of the ore-forming fluid and mechanism of Cu and Pb-Zn mineral precipitation are still unclear. The metallogenic process of the Baoshan Cu-Pb-Zn deposit can be divided into four stages: (1) the early skarn stage (S₁); (2) the late skarn stage (S₂); (3) the Cu-Fe sulfide stage (S₃); and (4) the Pb-Zn sulfide stage (S₄). The results of microtemperature measurements and a Raman spectrometric analysis of fluid inclusions show that the ore-forming fluid was the H₂O-NaCl (-CO₂ ± N₂ ± C₂H₆) system in the skarn stages (S₁ + S₂) and changed into the H₂O-NaCl-CO₂ (±N₂ ± C₂H₆) system in the sulfide stages (S₃ + S₄). The temperature (S₁: 436.6~548.2 °C; S₂: 344.1~435.1 °C; S₃: 134.1~413.1 °C; S₄: 183.9~261.0 °C) and salinity (S₁: 17.4~51.2 wt.%NaClequiv; S₂: 13.6~41.7 wt.%NaClequiv; S₃: 1.2~32.3 wt.%NaClequiv; S₄: 1.8~9.6 wt.%NaClequiv) showed a downward trend from the early to late stages. From the skarn stages (S₁ + S₂) to the sulfide stages (S₃ + S₄), the ore-forming pressure results from the static rock pressure and the hydrostatic pressure, and the ore-forming depth is estimated to be about three to six km. The C-H-O isotopic compositions of hydrothermal minerals such as quartz and calcite indicate that the ore-forming fluid is predominately magmatic fluid, but a significant amount of meteoric water is added in the Pb-Zn sulfide stage (S₄). The formation of the mineralization zonation of the Baoshan deposit is the result of many factors (e.g., stratigraphy, structure and metal precipitation mechanism): the Cu mineralization is controlled by the contact zone, and the Pb-Zn mineralization is controlled by the fault. In addition, the precipitation of Cu is mainly controlled by fluid boiling, while the precipitation of Pb and Zn is mainly controlled by the mixing of magmatic fluid and meteoric water. Full article

A calc–alkaline dioritic–andesitic–dacitic intrusive–volcanic complex of Early Oligocene (30 Ma) age and its Mesozoic sedimentary basement at Recsk host a well-preserved porphyry–skarn–polymetallic carbonate-replacement–epithermal mineral system. The unique occurrence offers an exceptional possibility to study these related mineralization types at a single locality. This study presents the textural–paragenetic, compositional characteristics, and systematics of sulfide mineral assemblages for the porphyry, skarn, and carbonate-replacement ore types, which are currently situated at a depth of 500–1200 m below the present surface. Detailed petrography combined with EPMA analyses of molybdenite, galena, sphalerite, tetrahedrite-group minerals and Bi-bearing sulfosalts allows for the establishment of characteristic mineral and chemical fingerprints for each mineralization type. Rhenium concentration in molybdenite, occurring as rare disseminations and quartz–carbonate veinlets in altered host rocks in all three mineralization types, shows a decreasing trend towards the more distal mineralization types. High Re contents ($\overline{\mathrm{x}}$ = 1.04 wt.%, max. up to 4.47 wt%) are typical for molybdenite from the porphyry mineralization, but Re is not homogeneously distributed, neither within individual molybdenite crystals nor on a mineralization scale. Copper and Se show opposite behavior in molybdenite, both becoming enriched in the more distal mineralization types. Silver, Bi, and Se concentrations increase in galena and tetrahedrite-group minerals, both towards the country rocks, making them the best candidates for vectoring within the whole hydrothermal system. For tetrahedrite-group minerals, Ag, Bi, Se, together with Sb and Zn, are the suitable elements for fingerprinting; all these are significantly enriched in the distal carbonate-replacement mineralization compared to the other, more proximal ore types. Additionally, further trends can be traced within the composition of sulfosalts. Lead-bearing Bi sulfosalts preferentially occur in the polymetallic carbonate-replacement veins, while being under-represented in the skarn and porphyry mineralization. Porphyry mineralization hosts Cu-bearing Bi sulfosalts dominantly, while skarn is characterized by Bi-dominated sulfosalts. Sphalerite, although present in all mineralization types, cannot be used for fingerprinting, vectoring, or thermobarometry based on EPMA measurements only. Trace element contents of sphalerite are low, often below the detection limits of the analyses. This is further complicated by the intense “chalcopyrite disease” occurring throughout the distal mineralization types. All the above-listed major, minor, and trace element ore mineral characteristics enable the characterization of the Recsk ores by mineral geochemical fingerprints, providing a possible vectoring tool in porphyry Cu–(Mo)–Au-mineralized systems. Full article

In this paper, the process of solid-state metalized reduction and magnetic separation was investigated for preparation of nickel–iron concentrate from a low-grade laterite nickel ore. The effects of reduction temperature, reduction time, amount of dosages, and magnetic field strength on grades and recoveries of nickel and iron were studied. The results showed that nickel–iron concentrate with a nickel grade of 7.32%, nickel recovery of 81.84%, iron grade of 78.74%, and iron recovery of 69.78% were obtained under the conditions of a reduction temperature of 1200 °C, reduction time of 120 min, calcium fluoride addition of 12%, ferric oxide addition of 10%, coal addition of 12%, and magnetic field strength of 170 kA/m. 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

Deep-sea polymetallic nodules are associated with rich rare substances, such as rare-earth elements (REEs), Mo, Ti, Te, Li, which are currently in demand and are used in various applications. Deep-sea sediments near nodules are another important source of REEs, which will increase the resource potential of polymetallic nodules. Given the similarity of the mining technologies for deep-sea REEs and polymetallic nodules, this study proposed environmentally friendly mining options and developed a technoeconomic evaluation model by combining deep-sea polymetallic nodules and REEs. Using the Clarion-Clipperton Fracture Zone as an example, this study revealed that the development of polymetallic nodules together with REEs of nearby sediments in the form of by-products will improve the economic and environmental benefits. In addition, the effects of discount rate, cost, and price on the economic benefits of nodule mining were discussed, and a technical development direction was proposed based on scientific and technological needs. Full article

Ore collection devices are important for the collection of deep-sea polymetallic nodules. Based on the CFD-DEM solid–liquid two-phase flow coupling calculation method, this paper simulated the rise and transport phases of polymetallic nodules using the Coanda effect ore collection device. The validity of the numerical simulation method was confirmed through experimental testing. On this basis, the effects of different working and structural parameters on the collection rate were studied. The results indicate that the flow rate of the collection jet and the bottom clearance were the primary factors affecting the collection rate of the polymetallic nodules. An increase in the collection jet flow rate leads to a substantial rise in the collection rate of polymetallic nodules. Conversely, an increase in bottom clearance results in a decrease in the collection rate. A collection rate exceeding 90% can be achieved in both scenarios: a 10 mm bottom clearance with an 8 m/s collection jet flow rate, and a 30 mm bottom clearance with a 10 m/s collection jet flow rate. The collection nozzle slant angle has no substantial impact on the collection rate, and the recommended collection nozzle slant angle is 35° to reduce energy loss. Full article

The results of studies on the content of aluminum and heavy metals in benthic sediments and algae in the estuaries of the Arctic island Vaygach are presented. This island is located on the Barents and Kara Sea border, and it is part of the Pay-Khoi ridge which can be called a “continuation” of the Ural Mountains to the north. The observations were conducted in Krasnaya and Varkulyakha Rivers located in the island’s southern part and flow into the Yugorsky Shar Strait. Krasnaya River is located near a polymetallic ore deposit, which was developed in 1931–1934. Reconnaissance fieldwork was carried out in the river estuaries through measurements of salinity and water level. Measurements of the mass concentration of elements in the studied samples of sediments and algae were carried out by atomic emission spectrometry. The preparation of plant samples was by microwave decomposition, and that for samples of bottom sediments was carried out by acid decomposition in an open manner. The obtained concentration samples were compared using “Tukey exploratory data analysis (EDA)”. The presence of anomalies in the high content of copper, manganese, and zinc in filamentous algae at the control site in the Krasnaya River estuary was revealed. For some elements, the enrichment index was calculated relative to the upper part of the earth’s crust content. It is assumed that the occurrence of this situation is due to the long-term consequences of mining polymetallic ores. The accumulation of metals in river estuaries may be related to the observed warming of the climate in the western sector of the Arctic region. Full article

Geochemical measurements of stream sediments are practical for small-scale mineral exploration. However, traditional grid interpolation methods cause element concentrations to diffuse and smooth out anomalies, particularly in complex terrains, making it challenging to reflect the actual distribution of elements accurately. We applied the Dynamic Enhanced Weighted Drainage Catchment Basin (DE-WDCB) method to enhance the retention and identification of local anomalies by limiting the scope of analysis to specific drainage units. This method reduces interference from varying background values across different watersheds, effectively enhancing geochemical element anomalies and aligning better with geomorphic conditions. The DE-WDCB method was tested in the Duobaoshan–Heihe area, a significant copper polymetallic mineral district in northeastern China. Compared with traditional grid interpolation methods, the DE-WDCB method retained and strengthened low and weak abnormal information of favorable mineralization elements, particularly in the Luotuowaizi area. The method demonstrated a higher spatial coverage rate with mineral points and a more vital ore-indicating ability. Specifically, the DE-WDCB method identified anomalies with a mean accuracy of 63.57% (p < 0.05, 95% CI: 47.64%–79.50%), compared to 50.53% for traditional methods. In conclusion, in regions with a complex topography and watershed differences, the DE-WDCB method effectively reduces local geochemical background interference, accurately identifies low and weak geochemical anomalies, and better reflects the actual distribution of elements. This makes it a significantly advantageous method for geochemical anomaly extraction, delineating higher-confidence exploration targets in the Sandaowan–Luotuowaizi area in the east and the triangular area between Duobaoshan, Yubaoshan, Sankuanggou, and the midstream highlands of the Guanbird River in the west. Full article

The Songpan–Ganzi Orogenic Belt (SGOB) is bounded by the South China, North China, and Qiangtang blocks and forms the eastern margin of the Tibetan Plateau. The Tiechanghe Granite is located at the junction of the southeast margin of the SGOB and the western margin of the Yangtze Block. To elucidate the genetic relationship between the Tiechanghe Granite and the surrounding molybdenum deposits in Western Sichuan, in this study, we conducted zircon U-Pb and molybdenite Re-Os isotopic dating. The results indicate that the Tiechanghe Granite predominantly consists of monzogranite, with minor occurrences of syenogranite, while the molybdenum deposits are mainly found in skarn and quartz veins. The laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) zircon U-Pb ages of the Tiechanghe Granite range from 162.9 ± 0.7 Ma (MSWD = 0.31, n = 25) to 163.4 ± 0.6 Ma (MSWD = 0.85, n = 26), and the LA-ICP-MS zircon U-Pb age of the pegmatite veins is 164.1 ± 0.9 Ma (MSWD = 1.3, n = 19). These ages are consistent with the weighted average Re-Os age of the Ziershi molybdenite (160.3 ± 1.6 Ma, n = 2) within the error margins. These findings and previously obtained magmatic and metallogenic ages for the region suggest that a magmatic and mineralization event involving granite, molybdenum, tungsten, and copper occurred at around 162–164 Ma in the study area. This discovery broadens the exploration perspective for mineral resources in the Jiulong area of Western Sichuan and the entirety of Western Sichuan. Full article

Baoshan is a world-class skarn Cu-polymetallic deposit located at the junction of the Nanling and Qin-Hang metallogenic belts in China. While there has been extensive research on the mineralogy and geochemistry of skarn deposits, studies on the fluid characteristics and evolutionary history from the early to late skarn stages in such deposits are still limited. In this study, we analyzed garnet and pyroxene from the early skarn stage and scheelite from the late skarn stage of the Baoshan deposit. We distinguished two generations of garnet (Grt1 and Grt2), one generation of pyroxene, and three generations of scheelite (Sch I, Sch II, and Sch III) on the basis of mineral assemblages and microscopic characteristics. Grt1 appears coarse-grained, and Grt2 cuts through Grt1 as veinlets. In Grt1, the andradite end-member increases from the core to the rim, while the grossular portion decreases (Ad_35–36Gr_59–61Sp_3–4 to Ad_59–61Gr_36–37Sp_2–3), and in Grt2, the andradite end-member significantly increases (Ad_41–73Gr_25–55Sp_2–3). Grt1 and Grt2 have similar trace element compositions, with enrichment in Zr and depletion in Nb and Hf, depletion in LREE, enrichment in HREE, and weak negative Eu anomalies. Pyroxene coexists with Grt1 and is similarly cut by Grt2, with its composition mainly being diopside (Di_82–99Hd_0.6–15Jo_0–3.2). Sch I and Sch II appear as anhedral to subhedral grains, while Sch III is predominantly found in veinlets. In Sch I and Sch II, most REEs enter the scheelite lattice via the Na-REE coupled substitution mechanism, with a smaller portion substituting Ca vacancies. In Sch III, the substitution mechanism involving Ca site vacancies may dominate. During the early skarn stage, the oxygen fugacity of the fluid gradually decreased from Grt1 and pyroxene to Grt2. In the late skarn stage, fluid oxygen fugacity remains stable from Sch I and Sch II to Sch III in shallow parts but significantly decreases in deeper parts. The garnet and pyroxene from the Baoshan deposit align with typical skarn Cu deposit compositions, while scheelite in the late skarn stage shows Sch I, Sch II, and shallow Sch III as skarn-type and deep Sch III as vein-type scheelite. Early skarn stage fluids were weakly acidic. Sch I, Sch II, and Sch III originated from fluids related to the Baoshan granite porphyry, with Sch III also showing evidence of water–rock interaction. This study reconstructed the fluid evolution history from the early to late skarn stages at the Baoshan deposit, providing insights into the ore-forming processes of other skarn deposits. Full article

To reduce the mercury content in flue gas from coal-fired power plants and to obtain high-performance, low-cost mercury adsorbents, a novel composite material was prepared by structural design through the in situ growth method. Functionalization treatments such as the modification of functional groups and multilayer loading of polymetallic were conducted. These materials include the MOF material UiO-66 and modified biochar doped with Fe/Ce polymetallic, both of which contain unsaturated metal centrals and oxygen-containing functional groups. On the basis of obtaining the effects of adsorption temperature and composite ratio on the Hg⁰ removal characteristics, coupling and synergistic mechanisms between the various types of active centers included were investigated by using a variety of characterization and analysis tools. The active adsorption sites and oxidation sites were identified during this process, and the constitutive relationship between the physicochemical properties and the performance of Hg⁰ removal was established. The temperature-programmed desorption technique, Grand Canonical Monte Carlo simulation, and adsorption kinetic model were employed to reveal the mechanism of Hg⁰ removal. The results showed that the UiO-66-Br@MBC composite adsorbent possessed an excellent Hg⁰ removal performance at adsorption temperatures ranging from 50 to 250 °C, and targeted construction of adsorption and oxidation sites while maintaining thermal stability. The Hg⁰ removal by the composites is the result of both adsorption and oxidation. The micropores and small pore mesopores in the samples provide physical adsorption sites. The modified biochar acts as a carrier to facilitate the full exposure of the central metal zirconium ions, the formation of more active sites, and the process of electron transfer. The doping modification of the Br element can enhance the overall redox ability of the sample, and the introduced Fe and Ce polymetallic ions can work in concert to promote the oxidation process of Hg⁰. The excellent regulation of the ratio between adsorption and oxidation sites on the surface of the composite material finally led to a significant boost in the samples’ capacity to remove Hg⁰. Full article

The Baoshan Cu-Pb-Zn deposit is situated at the intersection of the Qin-Hang Cu polymetallic and Nanling W-Sn polymetallic metallogenic belts. The age, lithology, petrogenesis, and tectonic setting of granodiorite porphyry within the deposit remain subjects of debate. Additionally, there is a lack of comparative studies with the W-Sn-related granites in the region. This study conducted whole-rock major and trace element analysis, Sr-Nd isotope analysis, and zircon U-Pb dating on the Baoshan granodiorite porphyry. The zircon U-Pb age of the granodiorite porphyry is 162 ± 1 Ma. The whole-rock SiO₂ and K₂O contents range from 65.87 to 68.21 wt.% and 3.42 to 5.62 wt.%, respectively, indicating that the granodiorite porphyry belongs to high-potassium calc-alkaline I-type granite. The granodiorite porphyry is characterized by enrichment in LREE and depletion in HREE (LREE/HREE ratio = 6.2–21.2). The samples of granodiorite porphyry generally exhibit weak negative Eu anomalies or no Eu anomalies (δEu = 0.62–1.04, mean = 0.82). The (⁸⁷Sr/⁸⁶Sr)_i and ε_Nd(t) values are 0.707717–0.709506 and −7.54 to −4.87, respectively. The whole-rock geochemical composition and Sr-Nd isotopic values indicate that the magma originated from the partial melting of the Mesoproterozoic ancient crust and Neoproterozoic mafic juvenile lower crust, with the addition of high oxygen fugacity and water-rich lithospheric mantle melts. The source of the granodiorite porphyry in the Baoshan deposit is significantly different from the crust-derived metapelite source of the W-Sn-related granite in the area, indicating that different magma sources might be the main reason for the co-spatial and nearly contemporaneous development of Cu-Pb-Zn and W-Sn mineralization in the southern Hunan region. Full article