Journal Description
Minerals
Minerals
is an international, peer-reviewed, open access journal of natural mineral systems, mineral resources, mining, and mineral processing. Minerals is published monthly online by MDPI.
- Open Access— free for readers, with article processing charges (APC) paid by authors or their institutions.
- High Visibility: indexed within Scopus, SCIE (Web of Science), GeoRef, CaPlus / SciFinder, Inspec, Astrophysics Data System, AGRIS, and other databases.
- Journal Rank: JCR - Q2 (Mining & Mineral Processing) / CiteScore - Q2 (Geology)
- Rapid Publication: manuscripts are peer-reviewed and a first decision is provided to authors approximately 18.7 days after submission; acceptance to publication is undertaken in 2.6 days (median values for papers published in this journal in the second half of 2023).
- Recognition of Reviewers: reviewers who provide timely, thorough peer-review reports receive vouchers entitling them to a discount on the APC of their next publication in any MDPI journal, in appreciation of the work done.
- Companion journal: Mining
Impact Factor:
2.5 (2022);
5-Year Impact Factor:
2.7 (2022)
Latest Articles
Unraveling Parent Rock and Mineral Influences in Tropical Weathering Profiles: REE, Nd and Sr Isotopic Geochemistry
Minerals 2024, 14(5), 470; https://doi.org/10.3390/min14050470 (registering DOI) - 28 Apr 2024
Abstract
This study aims to investigate the effects of parent rock and minerals on lateritic weathering. The study presents X-ray diffraction (XRD), whole-rock geochemistry, and Nd-Sr isotopic data for examining two profiles, 10 and 12 m thick, respectively, that illustrate the regional tropical weathering
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This study aims to investigate the effects of parent rock and minerals on lateritic weathering. The study presents X-ray diffraction (XRD), whole-rock geochemistry, and Nd-Sr isotopic data for examining two profiles, 10 and 12 m thick, respectively, that illustrate the regional tropical weathering status in the Midwest of Brazil. The profiles, developed from metasedimentary and sedimentary rocks, are constituted by saprolite, mottled horizon, lateritic duricrust, and oxisol. Across the profiles, the minerals controlling the weathering geochemistry are muscovite, microcline, quartz, kaolinite, hematite, goethite, and gibbsite. Red and yellow zones in the saprolite and mottled horizon as well as the lateritic duricrust with breccia/fragmental, pisolitic, and oolitic textures make profile 1 more complex. In contrast, profile 2 has an oxisol that mantles the homogeneous vermiform lateritic duricrust. Fe2O3, accumulated during surface weathering, is a potent element in the geochemical profile control since it forms the harder goethite to hematite lateritic duricrust, bearing most of the trace elements (As, Cu, Cs, Pb, Sc, Sr, Th, U, V, and Zn) with similar ionic radii and electrovalence. The LREE have affinity for the elements of the Fe2O3 group of the lateritic duricrust. On the other hand, the K2O group together with Zr and TiO2 e in the phyllite, saprolite, and mottled horizon of profile 1, are associated with the HREE. Additionally, in profile 2, the HREE are mostly associated with the Al2O3 group and the residual minerals in the oxisol. The indication that REE is associated with phosphates, zircon, rutile/anatase, cereanite, and muscovite/illite, which have variable weathering behavior, caused the REE fractionation to occur across and between the profiles. Despite the REE fractionation, the ƐNd(0) values along the profiles consistently maintain the signature of the parent rock. Muscovite and microcline weathering, in profiles 1 and 2, respectively, control the decrease in 87Sr/86Sr signatures of both profiles and the distinct radiogenic ratios. The development of lateritic duricrust in both profiles indicates a similar weathering intensity, although the gibbsite–kaolinite predominance in the oxisol of profile 2 highlights a geochemical reorganization under humid conditions, as well as near-intense soluble silica leaching.
Full article
(This article belongs to the Special Issue Understanding the Rock Weathering Process: Insights from Mineralogy and Geochemistry)
Open AccessArticle
Mineralogical Characterization of Raw Clay from Rujište (Serbia) Used in Traditional Pottery Manufacture
by
Maja Milošević, Predrag Dabić, Jelena Gulicovski, Vladimir Dodevski and Milena Rosić
Minerals 2024, 14(5), 469; https://doi.org/10.3390/min14050469 (registering DOI) - 28 Apr 2024
Abstract
The pottery produced from the Rujište deposit in Serbia has been protected under the guidance of UNESCO and the Sector for Intangible Cultural Heritage of Serbia since 2019. A study was conducted to evaluate the mineralogical characteristics of the raw clay from this
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The pottery produced from the Rujište deposit in Serbia has been protected under the guidance of UNESCO and the Sector for Intangible Cultural Heritage of Serbia since 2019. A study was conducted to evaluate the mineralogical characteristics of the raw clay from this deposit. This study used various techniques, such as X-ray diffraction (XRD), infrared (IR) spectroscopy, X-ray fluorescence (XRF), and differential thermal analysis (DTA) to characterize the clay. This study found that the clay contained mostly clay minerals (56.3%–41.9%), with illite, smectite, and chlorite as the predominant phases. Other phases identified were quartz, feldspars, carbonates, and iron-bearing minerals (43.8%–58.1%). The chemical analyses revealed a high abundance of silica (>52 wt.%) and alumina (~16 wt.%), with Fe2O3 (~6 wt.%), K2O (~2.8 wt.%), and a similar content of MgO as the main constituents. The physical features that were investigated included the granulometry (clay: ~31%–44%, silt: ~ 26%–23%, and sand: ~ 42%–32%), specific surface area (97 to 107 m2 g−1), cation exchange capacity (12.5–13.7 mmol 100 g−1), and color (yellowish to moderate brown). The preliminary results suggest that most of the raw clay from the Rujište deposit might be suitable for use in traditional pottery manufacture.
Full article
(This article belongs to the Section Crystallography and Physical Chemistry of Minerals & Nanominerals)
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Open AccessArticle
Improving the Flotation of Unoxidized and Oxidized Molybdenite Fines Using Dodecylamine as a Collector: Flotation Tests and Interaction Mechanism
by
Bingqiao Yang, Jie Wu, Bing Deng, Hui Shao, Shaoxian Song and Mildred Quintana
Minerals 2024, 14(5), 468; https://doi.org/10.3390/min14050468 (registering DOI) - 28 Apr 2024
Abstract
The flotation of unoxidized and oxidized molybdenite fines is a challenging job worldwide. In this work, dodecylamine (DDA) was developed as a potential collector to improve the flotation of molybdenite fines with and without oxidation. The flotation behaviors and interaction mechanisms were probed
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The flotation of unoxidized and oxidized molybdenite fines is a challenging job worldwide. In this work, dodecylamine (DDA) was developed as a potential collector to improve the flotation of molybdenite fines with and without oxidation. The flotation behaviors and interaction mechanisms were probed through flotation tests, contact angle, Zeta potential, Scanning Electron Microscope-Energy Dispersive Spectrometer(SEM-EDS), and X-ray Photoelectron Spectroscopy (XPS). The flotation tests revealed that DDA improved the flotation of unoxidized or oxidized molybdenite fines efficiently. The results of Zeta potential, contact angle, and SEM-EDS uncovered that a substantial number of DDA species adsorbed on both fresh and oxidized molybdenite faces and edges, thus enhancing their hydrophobicity. XPS analysis further manifested that RNH2 and RNH3+ adsorbed on the S atoms of fresh faces through hydrogen bonding. Meanwhile, RNH2 and RNH3+ mainly adsorbed on fresh edges via chemical bonding between amine groups and Mo sites and electrostatic force. For oxidized molybdenite, RNH2 and RNH3+ interacted with oxidized faces through hydrogen bonding while adsorbed on oxidized edges via hydrogen bonding and electrostatic interaction.
Full article
(This article belongs to the Special Issue Flotation of Fine-Grained Minerals)
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Open AccessArticle
Electrical Resistivity and Phase Evolution of Fe–N Binary System at High Pressure and High Temperature
by
Yunzhe Wang, Fan Yang, Chunhua Shen, Jing Yang, Xiaojun Hu and Yingwei Fei
Minerals 2024, 14(5), 467; https://doi.org/10.3390/min14050467 (registering DOI) - 28 Apr 2024
Abstract
Partitioning experiments and the chemistry of iron meteorites indicate that the light element nitrogen could be sequestered into the metallic core of rocky planets during core–mantle differentiation. The thermal conductivity and the mineralogy of the Fe–N system under core conditions could therefore influence
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Partitioning experiments and the chemistry of iron meteorites indicate that the light element nitrogen could be sequestered into the metallic core of rocky planets during core–mantle differentiation. The thermal conductivity and the mineralogy of the Fe–N system under core conditions could therefore influence the planetary cooling, core crystallization, and evolution of the intrinsic magnetic field of rocky planets. Limited experiments have been conducted to study the thermal properties and phase relations of Fe–N components under planetary core conditions, such as those found in the Moon, Mercury, and Ganymede. In this study, we report results from high-pressure experiments involving electrical resistivity measurements of Fe–N phases at a pressure of 5 GPa and temperatures up to 1400 K. Four Fe–N compositions, including Fe–10%N, Fe–6.4%N, Fe–2%N, and Fe–1%N (by weight percent), were prepared and subjected to recovery experiments at 5 GPa and 1273 K. These experiments show that Fe–10%N and Fe–6.4%N form a single hexagonal close-packed phase (ɛ-nitrides), while Fe–2%N and Fe–1%N exhibit a face-centered cubic structure (γ-Fe). In separate experiments, the resistivity data were collected during the cooling after compressing the starting materials to 5 GPa and heating to ~1400 K. The resistivity of all compositions, similar to the pure γ-Fe, exhibits weak temperature dependence. We found that N has a strong effect on the resistivity of metallic Fe under rocky planetary core conditions compared to other potential light elements such as Si. The temperature-dependence of the resistivity also revealed high-pressure phase transition points in the Fe–N system. A congruent reaction, ε ⇌ γ’, occurs at ~673 K in Fe–6.4%N, which is ~280 K lower than that at ambient pressure. Furthermore, the resistivity data provided constraints on the high-pressure phase boundary of the polymorphic transition, γ ⇌ α, and an eutectoid equilibrium of γ’ ⇌ α + ε. The data, along with the recently reported phase equilibrium experiments at high pressures, enable construction of a phase diagram of the Fe–N binary system at 5 GPa.
Full article
(This article belongs to the Special Issue Phase Transitions and Physical Properties of Minerals under Extreme Conditions of Pressure and Temperature)
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Open AccessArticle
Petrology and Geochemistry of an Unusual Granulite Facies Xenolith of the Late Oligocene Post-Obduction Koum Granodiorite (New Caledonia, Southwest Pacific): Geodynamic Inferences
by
Dominique Cluzel, Fabien Trotet and Jean-Louis Paquette
Minerals 2024, 14(5), 466; https://doi.org/10.3390/min14050466 (registering DOI) - 28 Apr 2024
Abstract
Pressure–temperature estimates of a xenolith found within a post-obduction granodiorite in southern New Caledonia provide evidence for subcrustal, granulite facies, peak crystallisation conditions (ca. 850 °C—8.5 ± 1.0 kbar), followed by isobaric cooling to 700 °C, and final decompression with partial rehydration at
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Pressure–temperature estimates of a xenolith found within a post-obduction granodiorite in southern New Caledonia provide evidence for subcrustal, granulite facies, peak crystallisation conditions (ca. 850 °C—8.5 ± 1.0 kbar), followed by isobaric cooling to 700 °C, and final decompression with partial rehydration at ca. 650 °C—3.5 kbar. The xenolith, dated at 24.7 Ma (U-Pb zircon), i.e., the same age as the granodiorite host rock, has low SiO2 (35.5 wt%) and high Al2O3 (33.2 wt%) contents, suggesting that it is the restite of a previous melting episode, while the elevated Ca (Ba and Sr) contents suggest mantle metasomatism. Although the concentrations of Rb, K, Ca, Ba, and Sr have been strongly modified, some geochemical (REE patterns and some “immobile” trace element ratios) and isotopic (Sr and Nd isotopic ratios, U-Pb zircon age) characteristics of the granulite facies xenolith are similar to those of the xenoliths found in other Late Oligocene intrusions in southern New Caledonia; therefore, this rock is interpreted to be related to an early magmatic episode. The rock protolith was emplaced and equilibrated at the base of the crust where it underwent ductile deformation. Younger ascending magma picked it up and they eventually crystallised together at a shallow crustal level, near the tectonic sole of the ophiolite. The recrystallisation and ductile deformation at ~8.5 kbar suggest that a rheological discontinuity existed at about 25–28 km, probably representing the Moho. It is concluded that a continental crust of normal thickness must have existed beneath New Caledonia at about 24 Ma, i.e., 10 Ma after obduction.
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(This article belongs to the Section Mineral Geochemistry and Geochronology)
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The Geology and Mineral Chemistry of Beryl Mineralization, South Eastern Desert, Egypt: A Deeper Insight into Genesis and Distribution
by
Mohamed Zaki Khedr, Gehad M. Saleh, Khaled M. Abdelfadil, Eiichi Takazawa, Kamal Abdelrahman, Akihiro Tamura and Shaimaa Ali El-Shafei
Minerals 2024, 14(5), 465; https://doi.org/10.3390/min14050465 (registering DOI) - 28 Apr 2024
Abstract
Beryl mineralization in the Nugrus-Sikait domain in the South Eastern Desert (SED) of Egypt occurs as disseminated crystals in granitic pegmatite and quartz, as well as pegmatite veins crosscutting mélange schist and ophiolitic rocks. When granitic pegmatite comes into contact with the ophiolitic
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Beryl mineralization in the Nugrus-Sikait domain in the South Eastern Desert (SED) of Egypt occurs as disseminated crystals in granitic pegmatite and quartz, as well as pegmatite veins crosscutting mélange schist and ophiolitic rocks. When granitic pegmatite comes into contact with the ophiolitic rocks, phlogopite and amphibole schists are formed due to K metasomatism. The ophiolitic mélange is intruded by leucogranite and related pegmatite along the NNW to NW Nugrus shear zone. Beryl samples have been collected from Um Sleimat, Madinat Nugrus, Wadi Abu Rusheid, and Wadi Sikait. Major oxides and in situ trace and rare earth elements (REEs) of beryl and associated minerals were analyzed through EPMA and LA-ICP-MS, respectively. The investigated beryl, based on its color and chemical compositions, can be classified into the two following types: pegmatitic beryl (type I) and schist-related beryl (type II). The former is colorless to pale green, and is mainly restricted in pegmatite veins; it is poor in Cr2O3 (up to 0.03 wt%) and MgO (Nil). The latter, deep green in color, is rich in Cr2O3 (up to 0.27 wt%) and MgO (up to 2.71 wt%), and occurs within quartz veins, phlogopite schists, and tremolite schists. The abundant beryl mineralization in phlogopite schists and their related quartz veins suggests that granite and associated pegmatite are the source rocks for the Be-bearing fluids that migrate along the NW-SE trending deep-seated tectonic zone, such as the Nugrus shear zone. Therefore, the formation of beryl in schists is attributed to the interaction of granitic/pegmatitic-derived Be-bearing fluids with serpentinite and gabbro interlayered with mélange schists. Variations in the trace and REE contents of both beryl types (I and II) indicate their two-stage formation from different compositions of Be-rich fluids, where light REEs, Zr, Nb, Ba, and Th decrease from type I beryl to type II. These two phases of beryl could be attributed to the magmatic/hydrothermal fluids associated with the pegmatite emplacement. The early phase of the late-stage magmatic-derived fluids was closely related to magma evolution and pegmatite formation, forming euhedral type I beryl. The late phase of pegmatite-derived fluids was mixed with serpentinite/schist-derived fluids that cause high V and Cr content in type II beryl. The composition of parent magmas of felsic rocks, the high degree of magma fractionation or the late stage melts, fluid compositions (rich in Be, Li, Cs, Rb, K), and alkali metasomatism, as well as the linear NW-SE trending deep-seated shear zone, are all factors possibly influencing beryl mineralization in the SED of Egypt.
Full article
(This article belongs to the Special Issue Geochemistry, Geochronology and Mineralization Styles Accompanying the Neoproterozoic Evolution of Orogenic Belts)
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Open AccessArticle
Selective Separation of Rare Earth Ions from Mine Wastewater Using Synthetic Hematite Nanoparticles from Natural Pyrite
by
Chunxiao Zhao, Jun Wang, Baojun Yang, Yang Liu and Guanzhou Qiu
Minerals 2024, 14(5), 464; https://doi.org/10.3390/min14050464 (registering DOI) - 28 Apr 2024
Abstract
The separation of rare earth ions (RE3+) from aqueous solutions poses a significant challenge due to their similar chemical and physical characteristics. This study presents a method for synthesizing hematite nanoparticles (Fe2O3 NPs) through the high-temperature phase transition
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The separation of rare earth ions (RE3+) from aqueous solutions poses a significant challenge due to their similar chemical and physical characteristics. This study presents a method for synthesizing hematite nanoparticles (Fe2O3 NPs) through the high-temperature phase transition of natural pyrite for adsorbing RE3+ from mine wastewater. The characteristics of Fe2O3 NPs were studied using XRD, SEM, BET, XPS, FTIR, and Zeta potential. The optimal condition for RE3+ adsorption by Fe2O3 NPs was determined to be at pH 6.0 with an adsorption time of 60 min. The maximum adsorption capacities of Fe2O3 NPs for La3+, Ce3+, Pr3+, Nd3+, Sm3+, Gd3+, Dy3+, and Y3+ were 12.80, 14.02, 14.67, 15.52, 17.66, 19.16, 19.94, and 11.82 mg·g−1, respectively. The experimental data fitted well with the Langmuir isotherm and pseudo-second-order models, suggesting that the adsorption process was dominated by monolayer chemisorption. Thermodynamic analysis revealed the endothermic nature of the adsorption process. At room temperature, the adsorption of RE3+ in most cases (La3+, Ce3+, Pr3+, Nd3+, Sm3+, and Y3+) onto Fe2O3 NPs was non-spontaneous, except for the adsorption of Gd3+ and Dy3+, which was spontaneous. The higher separation selectivity of Fe2O3 NPs for Gd3+ and Dy3+ was confirmed by the separation factor. Moreover, Fe2O3 NPs exhibited excellent stability, with an RE3+ removal efficiency exceeding 94.70% after five adsorption–desorption cycles, demonstrating its potential for the recovery of RE3+ from mine wastewater.
Full article
(This article belongs to the Section Mineral Processing and Extractive Metallurgy)
Open AccessReview
Gold Deposits Related to the Island Arc Formations and Ophiolitic Complexes of Eastern Cuba: A Review
by
Jorge L. Costafreda, Domingo A. Martín, Jorge L. Costafreda-Velázquez and José Luis Parra
Minerals 2024, 14(5), 463; https://doi.org/10.3390/min14050463 (registering DOI) - 28 Apr 2024
Abstract
Several gold deposits in the eastern region of Cuba are genetically related to the island arc- and the ophiolitic complex formation. These have been studied and exploited since the time of the Spanish colonization in the mid-sixteenth century. These deposits belong to the
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Several gold deposits in the eastern region of Cuba are genetically related to the island arc- and the ophiolitic complex formation. These have been studied and exploited since the time of the Spanish colonization in the mid-sixteenth century. These deposits belong to the Aguas Claras-Guajabales mineral field in the Holguín Province (Cuba) and lie in an elongated zone approximately 15 km in length. The object of this work is to make a methodical, detailed, and chronological review of the geological and mining work carried out in this region, as well as highlight the degree of the previously achieved studies. To realize this, an extensive bibliographic review of all available data, including published reports and articles, as well as unpublished material, was carried out. Moreover, ore mineralogy and petrography were reviewed by thin section analyses from samples from these deposits by petrographic and scanning electron microscopy. The results obtained from this study highlight that the gold mineralization in that area is closely linked to metasomatic processes produced by the circulation of hydrothermal fluids that affected the different volcanic and ultramafic rocks. This study shows that the highest gold contents observed are controlled by the contacts between the different host lithologies with high rheological contrasts. The presence of different alteration styles such as serpentinization, listvenitization, rodingitization, and propylitization have played a primary role in the deposition of gold during mineralization processes. This work could be a very useful exploration guide for future research in this region, as it provides a useful and practical compilation of the characteristics of the mineralization and alteration styles, as well as a precise indication of the spatial position, thicknesses, and contents of the gold-rich horizons.
Full article
(This article belongs to the Special Issue Mineralogy, Geochemistry and Fluid Inclusion Study of Gold Deposits Endowed in Critical Metals)
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Open AccessArticle
XPS Investigation of Magnetization Reduction Behavior and Kinetics of Oolitic Hematite in Gas-Based Roasting
by
Mengfei Li, Hanquan Zhang, Fan Yang, Tiejun Chen, Manman Lu and Hong Yu
Minerals 2024, 14(5), 462; https://doi.org/10.3390/min14050462 (registering DOI) - 28 Apr 2024
Abstract
Magnetization reduction roasting is an important method for the utilization of oolitic magnetite. In this study, the magnetization reduction behavior and kinetics of oolitic hematite in gas-based roasting were systematically investigated by X-ray photoelectron spectroscopy (XPS). The results revealed that under optimal roasting
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Magnetization reduction roasting is an important method for the utilization of oolitic magnetite. In this study, the magnetization reduction behavior and kinetics of oolitic hematite in gas-based roasting were systematically investigated by X-ray photoelectron spectroscopy (XPS). The results revealed that under optimal roasting conditions of 650 °C, a roasting time of 60 min, and a CO concentration of 30%, the magnetization reduction rate of the roasted product reached 44.34%. Furthermore, the weak magnetic separation concentrate presented a TFe of 58.09% and a concentrate iron recovery of 94.3%. The results of the XPS spectrum indicated that the peak area ratio (Fe2+/Fe3+) gradually increased with an increase in roasting temperature, roasting time, and CO concentration, while over-reduction occurred when the roasting temperature exceeded 750 °C. The investigation of magnetization roasting kinetics for varying particle sizes demonstrated that the magnetization reduction process is controlled by chemical reaction, with a corresponding activation energy range of 42.96 kJ/mol to 63.29 kJ/mol, indicating the particle size has little effect on the magnetization reduction of oolitic hematite.
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(This article belongs to the Special Issue Flotation of Fine-Grained Minerals)
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Geochemical Characteristics and Sedimentary Paleoenvironment of the Coal-Bearing Strata in the Xishanyao Formation: A Case Study of the Yihua Coal Mine in the Zhundong Coalfield, Xinjiang
by
Yulong Wang, Wenfeng Wang, Wenlong Wang and Piaopiao Duan
Minerals 2024, 14(5), 461; https://doi.org/10.3390/min14050461 - 26 Apr 2024
Abstract
The eastern Junggar Basin in Xinjiang harbors abundant coal resources within the Middle Jurassic Xishanyao Formation. However, the formation environment associated with these coal-bearing strata remains unclear. Geochemical characteristics serve as crucial geological indicators of the sedimentary period. Therefore, it is imperative to
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The eastern Junggar Basin in Xinjiang harbors abundant coal resources within the Middle Jurassic Xishanyao Formation. However, the formation environment associated with these coal-bearing strata remains unclear. Geochemical characteristics serve as crucial geological indicators of the sedimentary period. Therefore, it is imperative to explore the geochemical attributes and sedimentary context of the coal-rich layers within the Middle Jurassic Xishanyao Formation in the Zhundong region to enhance the prospects of coal extraction and utilization. The elemental compositions, both major and trace, of the Xishanyao Formation were analyzed through X-ray fluorescence spectrometry (XRF) and inductively coupled plasma mass spectrometry (ICP-MS). A comprehensive analysis was conducted on the sediment provenance, tectonic background, and depositional environment of the coal-bearing strata in the Xishanyao Formation. Moreover, through the utilization of a range of discrimination indices, including Sr/Cu, B/Ga, Sr/Ba, V/Cr, Ni/Co, and δCe, the paleo-depositional setting of the coal-containing layers was reconstructed. The findings suggest that the primary source rocks of the coal-bearing beds in the Xishanyao Formation consist of continental tholeiites, with the predominant material composition in the source region being felsic volcanic rocks originating from the upper crust. The tectonic backdrop of the source region is marked by a continental island arc environment. During the sedimentation period of the Xishanyao Formation, the depositional environment was characterized by a freshwater oxidizing setting. Additionally, it experienced a transition from arid-hot to humid-hot before returning to arid-hot conditions.
Full article
(This article belongs to the Special Issue Geochemistry and Mineralogy of Coal-Bearing Rocks, 2nd Edition)
Open AccessArticle
Evaluation of the Durability of Concrete with the Use of Calcined Clays and Limestone in Salinas, Ecuador
by
Juan Francisco Garces-Vargas, Yosvany Díaz-Cardenas and Jose Fernando Martirena Hernandez
Minerals 2024, 14(5), 460; https://doi.org/10.3390/min14050460 - 26 Apr 2024
Abstract
This study aims at the evaluation of different formulations of concrete made with calcined clays and limestone (LC3 cement) exposed to aggressive environments. The study includes the evaluation of fresh and hardened properties and a comprehensive evaluation of durability over 24 months. The
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This study aims at the evaluation of different formulations of concrete made with calcined clays and limestone (LC3 cement) exposed to aggressive environments. The study includes the evaluation of fresh and hardened properties and a comprehensive evaluation of durability over 24 months. The inclusion of calcined clays in cement increases the specific surface area of the cements, and thus the water demand. However, the high reactivity of calcined clays compared to any other pozzolan, and the synergy that occurs with limestones, enables the use of cements with very low clinker content that achieve strengths similar to those of Portland. Comparisons of LC3 formulations with Portland cement and with concrete containing silica fume prove the superiority of calcined clays in terms of strength and durability. The best results are obtained with LC3-50 cement with 50% clinker produced through co-grinding. Results of concrete made with a blend of 70% Portland cement with 30% LC2 (60% calcined clay, 35% limestone, 5% gypsum, separate ground) are also promising. All concretes made with LC3 show good durability in terms of the results of effective porosity, chloride permeability, and resistivity tests.
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(This article belongs to the Special Issue Applications of Clay-Based Materials)
Open AccessArticle
Dynamic Climate Influence on Magnesium Isotope Variation in Saline Lacustrine Dolomite: A Case Study of the Qianjiang Formation, Jianghan Basin
by
Tianyu Wang, Kun Ling, Ren Wei and Lin Dong
Minerals 2024, 14(5), 459; https://doi.org/10.3390/min14050459 - 26 Apr 2024
Abstract
The investigation of magnesium (Mg) isotopes in dolomite has mainly focused on marine dolomite environments, leaving a significant gap in the understanding of their dynamics within lacustrine settings, especially in saline lake basins. In this study, a total of 16 sediment core samples
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The investigation of magnesium (Mg) isotopes in dolomite has mainly focused on marine dolomite environments, leaving a significant gap in the understanding of their dynamics within lacustrine settings, especially in saline lake basins. In this study, a total of 16 sediment core samples from Well BX-7 in the Qianjiang Depression were sequentially selected for scanning electron microscope observation, whole-rock analysis for major and minor elements, and isotopic measurements including δ18Ocarb, δ13Ccarb, δ26Mgdol, and δ26MgSi. In addition, two intact cores were subjected to detailed analysis on the centimeter scale. Sedimentation models were established to elucidate dolomite formation under contrasting climatic conditions, specifically humid climates with a significant riverine Mg input versus relatively dry conditions with a lower Mg input. Furthermore, a quantitative model was developed to assess the magnesium flux and isotopic mass balance within lacustrine systems, simulating the magnesium isotope variations in lake water under different climatic scenarios. The dolomite sample data at a smaller scale (sampling interval ≈ 3~5 mm) demonstrate a consistent trend with the established model, providing additional confirmation of its reliability. Dolomite precipitated under humid climatic conditions exhibits a lower and relatively stable δ26Mgdol, lower δ18O, and higher CIA, indicating higher river inputs and relatively stable Mg isotope values of lake water controlled by river input. Nevertheless, dolomite formed under relatively dry climatic conditions shows a relatively high δ26Mgdol, higher δ18O, and lower CIA, suggesting reduced river inputs and weathering intensity, as well as relatively high magnesium isotope values of the lake water controlled by dolomite precipitation. This study contributes to the understanding of magnesium isotopes in lacustrine dolomite systems.
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(This article belongs to the Special Issue Sedimentary Basins: Sedimentation, Stratigraphy, Petrology and Tectonics)
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Open AccessArticle
Nephrite from Xinjiang Qiemo Margou Deposit: Gemological and Geochemical Insights
by
Ting Fang, Yuan Chang and Mingxing Yang
Minerals 2024, 14(5), 458; https://doi.org/10.3390/min14050458 - 26 Apr 2024
Abstract
The nephrite belt in the Altun Mountain–Western Kunlun Mountain region, which extends about 1300 km in Xinjiang, NW China, is the largest nephrite deposit in the world. The Qiemo region in the Altun Mountains is a crucial nephrite-producing area in China, with demonstrated
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The nephrite belt in the Altun Mountain–Western Kunlun Mountain region, which extends about 1300 km in Xinjiang, NW China, is the largest nephrite deposit in the world. The Qiemo region in the Altun Mountains is a crucial nephrite-producing area in China, with demonstrated substantial prospects for future exploration. While existing research has extensively investigated secondary nephrite deposits in the Karakash River and native black nephrite deposits in Guangxi Dahua, a comprehensive investigation of black nephrite from original deposits in Xinjiang is lacking. Margou black-toned nephrite was recently found in primary deposits in Qiemo County, Xinjiang; this makes in-depth research on the characteristics of this mine necessary. A number of technical analytical methods such as polarizing microscopy, Ultra-Deep Three-Dimensional Microscope, electron microprobe, back-scattered electron image analysis, X-ray fluorescence, and inductively coupled plasma mass spectrometry were employed for this research. An experimental test was conducted to elucidate the chemical and mineralogical composition, further clarifying the genetic types of the black and black cyan nephrite from the Margou deposit in Qiemo, Xinjiang. The results reveal that the nephrite is mainly composed of tremolite–actinolite, characterized by Mg/(Mg + Fe2+) ratios ranging from 0.86 to 1.0. Minor minerals include diopside, epidote, pargasite, apatite, zircon, pyrite, and magnetite. Bulk-rock rare earth element (REE) patterns exhibit distinctive features, such as negative Eu anomalies (δEu = 0.00–0.17), decreasing light REEs, a relatively flat distribution of heavy REEs, and low total REE concentrations (1.6–38.9 μg/g); furthermore, the Cr (6–21 μg/g) and Ni (2.5–4.5 μg/g) contents are remarkably low. The magmatic influence of granite appears to be a fundamental factor in the genesis of the magnesian skarn hosting Margou nephrite. The distinctive black and black cyan colors are attributed to heightened iron content, mainly associated with FeO (0.08~6.29 wt.%). Analyses of the chemical composition allow Margou nephrite to be classified as typical of magnesian skarn deposits.
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(This article belongs to the Special Issue Gem Deposits: Mineralogical and Gemological Aspects, 2nd Edition)
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In Situ Geochemical Evaluation of Retrograde Hydration Effects in the Peri-Siberian Forearc Mantle (Khara-Nur and Alag-Khadny Peridotite Complexes)
by
Anas A. Karimov, Marina A. Gornova, Vasiliy A. Belyaev, Sergei Yu. Skuzovatov, Alexander Ya. Medvedev and Nikolay V. Bryanskiy
Minerals 2024, 14(5), 457; https://doi.org/10.3390/min14050457 - 26 Apr 2024
Abstract
In order to assess the geochemical effects of retrograde metamorphic rehydration, fluid metasomatism, and the fluid-mobile elements (FMEs) budget in the case of oceanic and continental subduction, we report the petrography, bulk, and in situ LA-ICP-MS trace-element data for the two poorly studied
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In order to assess the geochemical effects of retrograde metamorphic rehydration, fluid metasomatism, and the fluid-mobile elements (FMEs) budget in the case of oceanic and continental subduction, we report the petrography, bulk, and in situ LA-ICP-MS trace-element data for the two poorly studied ophiolites in the northern (Khara-Nur, Eastern Sayan, Russia) and central (Alag-Khadny accretionary wedge, SW Mongolia) parts of the peri-Siberian orogenic framing. Both complexes are relics of the ancient oceanic mantle, which was subjected to processes of partial melting, metasomatism, and retrograde metamorphism. Typical mineral assemblages include olivine + orthopyroxene + chlorite + tremolite ± secondary olivine (640–800 °C), olivine + antigorite ± secondary clinopyroxene (<640 °C), and olivine + chrysotile ± secondary clinopyroxene (<250 °C) and are stable at pressures up to 2 GPa. Hydration and partial serpentinization of mantle peridotites lead to tremolite formation after orthopyroxene, followed by olivine replacement by antigorite. Serpentine-group minerals (antigorite and chrysotile) were distinguished by Raman spectroscopy, and the contents of incompatible elements (mobile and immobile in fluids) in metamorphic minerals (tremolite, antigorite, and chrysotile) were examined in situ by LA-ICP-MS. The behavior of conservative HFSE (Zr, Nb, Ta, and Ti) and—in part—HREE does not distinguish between the two types (oceanic and continental) of subduction environments. Different patterns of FMEs (Cs, Rb, Ba, U, Sb, Pb, Sr, and LREE) enrichment in metaperidotites reflect variations in the slab fluid composition, which was primarily governed by the contrasting nature of subducted lithologies. The affinity of Alag-Khadny to the subduction of a continental margin is recorded by increased FME contents and selective enrichment by some moderately mobile elements, such as U, Th, and LREE, with respect to the oceanic-type subduction environment of Khara-Nur. Distinct patterns of FME enrichment in tremolite and antigorite from two complexes indicate different sequences of fluid-induced replacement, which was controlled by Opx composition. We demonstrate that evaluation of the initial composition of precursor minerals affected by multi-stage melting and melt metasomatism should be considered with care to estimate the differential fluid overprint and associated elemental uptake from subduction fluids.
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(This article belongs to the Section Mineral Geochemistry and Geochronology)
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In-Situ Geochemical and Rb–Sr Dating Analysis of Sulfides from a Gold Deposit Offshore of Northern Sanshandao, Jiaodong Peninsula, North China: Implications for Gold Mineralization
by
Jiepeng Tian, Jinhui Wang, Tongliang Tian, Ligong Wang, Yingpeng Wang, Xiaowei Yu, Wen Zhang, Tianlong Ren and Bin Sun
Minerals 2024, 14(5), 456; https://doi.org/10.3390/min14050456 - 26 Apr 2024
Abstract
The gold deposit offshore of Northern Sanshandao is an ultra-large-scale gold deposit discovered in the Jiaodong ore area in recent years. This deposit is a fractured-zone altered-rock-type gold deposit; however, its ore genesis and precise mineralization processes are still highly controversial. Based on
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The gold deposit offshore of Northern Sanshandao is an ultra-large-scale gold deposit discovered in the Jiaodong ore area in recent years. This deposit is a fractured-zone altered-rock-type gold deposit; however, its ore genesis and precise mineralization processes are still highly controversial. Based on petrographical observation, the trace elements, sulfur isotopes, and rubidium–strontium isotopes of the gold-bearing pyrite were analyzed using LA-MC-ICP-MS to obtain the source of the ore-forming fluids and ore genesis. The results show that Au has a good positive correlation with Ag, As, and Cu. It is speculated that the As in the pyrite of the gold deposit offshore of Northern Sanshandao is in the form of As−, replacing S− and entering the pyrite, causing its lattice defects, and thus promoting the entry of Au+ into the gold-bearing pyrite. The Co/Ni ratios mainly range between 0.1 and 10, indicating that the mineralization process has experienced different forms of hydrothermal evolution and the mixing of different fluids. The results of the in-situ sulfur isotope analysis show that pyrite δ34S in the mineralization period is characterized by a high sulfur value. The authors of this study believe that the initial sulfur isotope composition has mantle-derived components. The large-scale, deep cutting, and high degree of fragmentation in the Sanshandao fault zone are conducive to the interaction between fluids and rocks, as well as the mixing and addition of seawater, resulting in the characteristic high δ34S value. The Sr isotopic compositions indicate a crust–mantle mixing attribute of the mineralized material source. The Rb–Sr isochron age of the pyrite is 118.5 ± 0.65 Ma, which represents the age of gold mineralization. According to the characteristics of the trace elements and sulfur isotopes, it is inferred that the gold deposit minerals offshore of Northern Sanshandao originated from deep magmatic-hydrothermal reservoirs, and the mixing of seawater and Au–As-rich hydrothermal fluids was the formation mechanism of huge amounts of gold precipitation.
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(This article belongs to the Special Issue Multi-Method (Geo-) Thermochronology and Trace Elements Tracing Magmatism, Mineralization and Tectonic Evolution)
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Open AccessArticle
Electrochemical Behavior of Natural Manganese Oxides: Transforming Mining Waste into Energy Storage Materials
by
George Soulamidis, Maria Kourmousi, Christiana A. Mitsopoulou and Christina Stouraiti
Minerals 2024, 14(5), 455; https://doi.org/10.3390/min14050455 - 26 Apr 2024
Abstract
The present research explores the potential of manganese oxide waste ore in energy storage applications, focusing on supercapacitors. The investigation assesses the electrochemical capabilities of natural manganese oxides obtained from the Drama region, which has been the main mining center of Greece for
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The present research explores the potential of manganese oxide waste ore in energy storage applications, focusing on supercapacitors. The investigation assesses the electrochemical capabilities of natural manganese oxides obtained from the Drama region, which has been the main mining center of Greece for manganese ore, especially that of battery-grade quality. Samples were collected from abandoned mining sites in the Kato Nevrokopi area, Drama. The structure and composition of the manganese minerals were determined by X-ray diffraction (XRD) and transmission electron microscopy (TEM). Electrochemical tests involved the preparation of electrodes using natural nsutite and heat-treated nsutite (hausmannite). Then, the designed electrodes were subjected to cyclic voltammetry tests and charge–discharge measurements. The hausmannite electrode exhibited a higher specific capacitance of 667 F/g at a current density of 0.2 A/g, and the electrode material retained 98.3% of its initial capacitance after 1000 cycles. This study provides new perspectives on simple and efficient methods for transforming natural nsutite material from mining waste to hausmannite with greater structural homogeneity and better electrochemical behavior.
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(This article belongs to the Special Issue Exploration, Mining, and Processing of Minerals: Enabling the Clean Energy Transition)
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The Measurement Reliability of δ13C of Dissolved Organic Carbon: A Validation for Speleothem Samples
by
Gang Xue, Yanjun Cai, Peng Cheng, Le Ma, Xing Cheng, Shouyi Huang and Yanbin Lu
Minerals 2024, 14(5), 454; https://doi.org/10.3390/min14050454 - 25 Apr 2024
Abstract
The carbon isotopic composition of dissolved organic carbon (δ13CDOC) in speleothems, based on high-precision U-Th ages, has great potential to reconstruct past ecology, microbial activity, and carbon cycling. Identifying the reliability of the pretreatment and measurement of speleothem δ
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The carbon isotopic composition of dissolved organic carbon (δ13CDOC) in speleothems, based on high-precision U-Th ages, has great potential to reconstruct past ecology, microbial activity, and carbon cycling. Identifying the reliability of the pretreatment and measurement of speleothem δ13CDOC is therefore essential to putting it into practice. Actually, we have previously verified the reliability of the method for speleothem δ13CDOC measurements. However, it was only based on the final δ13CDOC values of homogeneous speleothem powder and is unable to evaluate the effects of different experimental conditions and the impacts of adding acid on δ13CDOC if using speleothem as the study samples. In this study, we used an organic reagent (potassium sorbate) as the study sample and designed a conditional experiment that simulates the protocols for speleothem δ13CDOC analysis and presented the resulting data to inspect the effects of the experimental processes on the analysis of δ13CDOC. The results show that the standard deviation of duplicate samples is 0.1‰, which is close to that of the previous work for organic reagents and water samples, and the results were not affected by different experimental conditions and operation steps (such as adding orthophosphoric acid, digestion time, and storage duration of resulting CO2 in storage vessels), suggesting that this method is robust to detect the speleothem δ13CDOC. Considering the range and standard deviation of results, we proposed that the δ13CDOC record could be used in various studies when the amplitudes of the δ13CDOC record are larger than 0.1‰, especially greater than 0.4‰.
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(This article belongs to the Special Issue Stalagmite Geochemistry and Its Paleoenvironmental Implication)
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Coupled Processes at Micro- and Macroscopic Levels for Long-Term Performance Assessment Studies of Nuclear Waste Repositories
by
Hua Shao, Eike Radeisen, Jürgen Hesser, Wenqing Wang and Olaf Kolditz
Minerals 2024, 14(5), 453; https://doi.org/10.3390/min14050453 - 25 Apr 2024
Abstract
Performance assessment of nuclear waste repositories requires state-of-the-art knowledge of radionuclide transport properties. Additionally, the short-term development under thermal pulses and the long-term development of the near field—due to influences such as gas generation—must be evaluated. Key thermal-hydro-mechanical-chemical processes are strongly coupled on
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Performance assessment of nuclear waste repositories requires state-of-the-art knowledge of radionuclide transport properties. Additionally, the short-term development under thermal pulses and the long-term development of the near field—due to influences such as gas generation—must be evaluated. Key thermal-hydro-mechanical-chemical processes are strongly coupled on different spatial and temporal scales. To understand these coupling mechanisms, numerous material models and numerical codes have been developed. However, the existing constitutive approaches—which have been adapted to describe small-scale laboratory experiments and validated against real-scale field observations—are often unable to capture long-term material behavior with sufficient precision. To build the confidence, a more comprehensive understanding of the system at micro- and macroscopic scales is required. Most observed macroscopic processes result from microscopic changes in the crystal structure and/or crystalline aggregates, as well as changes in material properties under the influence of various factors. To characterize these physical fields in crystals, microscopic investigations, such as visualization, or geophysical methods are introduced to verify the understanding at the microscale. Two cases are demonstrated for the presented concept using microscale information: one deals with the mechanically and thermally driven migration of fluid inclusions in rock salt, the other with dilatancy-controlled gas transport in water-saturated clay material.
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(This article belongs to the Special Issue Implications of THMC Processes on Long-Term Safety of Geological Disposal of Radioactive Waste)
Open AccessReview
Igneous Diversity of the Early Martian Crust
by
Valerie Payré, Arya Udry and Abigail A. Fraeman
Minerals 2024, 14(5), 452; https://doi.org/10.3390/min14050452 - 25 Apr 2024
Abstract
Mars missions and Martian meteorites revealed how complex the Martian crust is. The occurrence of both alkaline and sub-alkaline igneous rocks of Noachian age (>3.7 Ga) in Gale crater indicates diverse magmatic processes, with sub-alkaline rocks likely formed through the partial melting of
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Mars missions and Martian meteorites revealed how complex the Martian crust is. The occurrence of both alkaline and sub-alkaline igneous rocks of Noachian age (>3.7 Ga) in Gale crater indicates diverse magmatic processes, with sub-alkaline rocks likely formed through the partial melting of hydrous mafic rocks, as commonly observed on Earth. The orbital discovery of excavated evolved igneous rocks scattered in Noachian terrains raise questions about the petrology of the ancient Martian crust, long thought to be basaltic. A possibly evolved crust beneath a mafic cover is supported by geophysical and seismic measurements from the Insight lander that indicate the bulk crust has a lower density than expected if it were homogeneously basaltic. If localized magmatic processes could form evolved terrains, the detection of abundant intermediate to felsic Noachian crustal exposures through remote sensing suggest regional- to global-scale processes that produced evolved crustal component(s) that are now buried below mafic materials. Due to the lack of centimetric to millimetric textural imaging and compositional measurements, the petrology of such crust is ambiguous. Future orbiter, rover, and aerial missions should focus on Noachian exposed regions exhibiting evolved crustal characteristics to unfold the petrology of the Martian crust and its formation.
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(This article belongs to the Special Issue Mineralogy and Geochemistry of Mars: Everything You Need to Know about the Red Planet)
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Effect of Fractionation Columns on the Elution of Rare Earth Elements Recovered from Acid Mine Drainage
by
Gabriela Cordeiro Silva, Clauson Souza, Pedro Augusto Possa Vicente Sacramento Ferreira, Liliani Pacheco Tavares Nazareth and Ana Claudia Queiroz Ladeira
Minerals 2024, 14(5), 451; https://doi.org/10.3390/min14050451 - 25 Apr 2024
Abstract
Rare earth elements (REE) can be found in expressive contents in different secondary sources, such as acid mine drainage (AMD). This work evaluated separation of light and heavy rare earth elements (REE) from an acid mine drainage (AMD) generated in a former uranium
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Rare earth elements (REE) can be found in expressive contents in different secondary sources, such as acid mine drainage (AMD). This work evaluated separation of light and heavy rare earth elements (REE) from an acid mine drainage (AMD) generated in a former uranium mine in Brazil by using ion exchange. This AMD presents pH 3.50, total REE content of 97 mg L−1 and 1.3 g L−1 of sulfate and was used in the REE loading experiments. Loading experiments were carried out in columns using a commercial strong acid cation (SAC) exchange resin. Elution was performed with 0.01 mol L−1 NH4EDTA in systems with one, two and three columns. Regarding the loading step, the resin presented a total loading capacity of 0.58 mmol g−1. The resin proved to be more selective for light REE with adsorption efficiency of 78% and 48% for heavy REE. Regarding elution, high efficiencies between 90 and 100% were achieved for REE. The final REE solution is approximately 10 times more concentrated in the liquor related to the acid mine water. Better fractionation results were achieved for the system with three columns. Although the complete separation of the REE into pure elements was not possible, two distinct fractions of heavy and light REE could be obtained, and La was completely separated from the other REE. In order to improve fractionation and separate the REE into individual ones, the concentrated fractions can proceed to subsequent ion exchange systems.
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(This article belongs to the Special Issue Characterization and Management of Mine Waters)
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