Previous Issue
Volume 15, August
 
 

Minerals, Volume 15, Issue 9 (September 2025) – 90 articles

  • Issues are regarded as officially published after their release is announced to the table of contents alert mailing list.
  • You may sign up for e-mail alerts to receive table of contents of newly released issues.
  • PDF is the official format for papers published in both, html and pdf forms. To view the papers in pdf format, click on the "PDF Full-text" link, and use the free Adobe Reader to open them.
Order results
Result details
Section
Select all
Export citation of selected articles as:
19 pages, 6850 KB  
Article
Geochronology and Geochemistry of the Galale Cu–Au Deposit in the Western Segment of the Bangong–Nujiang Suture Zone: Implications for Molybdenum Potential
by Chang Liu, Zhusen Yang, Xiaoyan Zhao and Jingtao Mao
Minerals 2025, 15(9), 975; https://doi.org/10.3390/min15090975 (registering DOI) - 15 Sep 2025
Abstract
The Galale Cu–Au deposit lies on the northern margin of the western Gangdese metallogenic belt, near the western edge of the Gangdese arc within the Bangong–Nujiang suture zone. Unlike the well-studied Miocene Cu belt in southern Gangdese, this region remains insufficiently investigated, particularly [...] Read more.
The Galale Cu–Au deposit lies on the northern margin of the western Gangdese metallogenic belt, near the western edge of the Gangdese arc within the Bangong–Nujiang suture zone. Unlike the well-studied Miocene Cu belt in southern Gangdese, this region remains insufficiently investigated, particularly in terms of geochemical characterization, leading to an ambiguous metallogenic model and a debated tectonic setting—specifically, the unresolved issue of subduction polarity across the Bangong–Nujiang suture. This tectonic ambiguity has important implications for understanding magma sources, metal transport pathways, and, consequently, for guiding mineral exploration strategies in the area. To address this, we conducted zircon U–Pb dating on the ore-related quartz diorite and granodiorite, yielding crystallization ages of 84.05 ± 0.34 Ma and 77.20 ± 0.69 Ma, respectively. Integrated with previous data, these results constrain mineralization to 83–89 Ma, which includes both skarn-type Cu–polymetallic and porphyry-type Cu mineralization. Regional comparisons support a tectonic model involving slab rollback and southward subduction of the Bangong–Nujiang oceanic lithosphere. Geochemical analyses of quartz diorite, granodiorite, and monzonitic granite show high-K calc-alkaline, peraluminous I-type affinities, with enrichment in LREEs and LILEs, and depletion in HREEs and HFSEs. Notably, the monzonitic granite is marked by high SiO2, Sr/Y, and Rb/Sr ratios, low Zr/Hf, strong LREE enrichment, weak Eu anomalies, and pronounced Nb–Ta depletion, indicating high oxygen fugacity and favorable conditions for Mo mineralization. The deposit formed through tectono-magmatic processes related to the closure of the Bangong–Nujiang Neo-Tethys Ocean. Subduction and subsequent lithospheric delamination induced partial melting of mantle and crustal sources, generating quartz diorite and granodiorite intrusions. Magmatic fluids interacted with carbonate wall rocks to form skarn assemblages, concentrating ore metals along structures. The mineralization formed within the contact zones between intrusions and surrounding country rocks. Late-stage granite porphyry intrusions (~77 Ma), inferred from major, trace, and rare earth element compositions to have the highest Mo potential, may represent an extension of earlier skarn mineralization in the area (83–89 Ma). This study presents the first comprehensive geochemical dataset for the Galale deposit, refines its metallogenic model, and identifies key geochemical indicators (e.g., Sr, Y, Nb, Rb, Zr, Hf) for Mo exploration. Full article
Show Figures

Figure 1

16 pages, 1097 KB  
Article
Composition, Properties, and Flotation Reagent Regimes of Carbonaceous Material
by Akim Yergeshev, Rustam Tokpayev, Marina Karmeeva, Tamina Khavaza, Mikhail Nauryzbayev and Vladislava Ignatkina
Minerals 2025, 15(9), 974; https://doi.org/10.3390/min15090974 (registering DOI) - 14 Sep 2025
Abstract
The novelty of this study lies in the first comparative characterisation of five carbonaceous materials: three monophase carbons (wood charcoal, carbon, graphite) and two ore-derived CM samples from polymetallic sulphide and oxidised lithium ores. The methodology included IR spectroscopy, XPS, acid–base adsorption centres [...] Read more.
The novelty of this study lies in the first comparative characterisation of five carbonaceous materials: three monophase carbons (wood charcoal, carbon, graphite) and two ore-derived CM samples from polymetallic sulphide and oxidised lithium ores. The methodology included IR spectroscopy, XPS, acid–base adsorption centres identified by colour indicators, chemical composition analysis, and kinetic flotation tests. Bulk and surface compositions differed significantly: although the ash content of ore-derived CM reached 84.4%, XPS revealed carbon-enriched surfaces with thin films of about 1–2 nm. IR spectra confirmed multiphase structures with carbonate, silica, and aluminosilicate bands, and showed an identical composition of CM from different industrial ore types. Flotation kinetics confirmed high floatability (recoveries 80%–99%, k up to 1.95 min−1). Even with sodium lignosulphonate at 500 mg/L, recovery only decreased from 83.02% to 52.54%, showing the limited efficiency of depressants. These results provide a basis for the preliminary removal of CM prior to rough (bulk) flotation in the processing of different ore types, improving concentrate quality, reducing reagent consumption, and lowering metallurgical losses. Full article
(This article belongs to the Special Issue Mineral Processing and Recycling Technologies for Sustainable Future)
Show Figures

Figure 1

13 pages, 2034 KB  
Article
Rare Earth Elements in Bottom Sediments of the Northern Part of Lake Umbozero, Murmansk Region, Russia
by Eugenia Krasavtseva, Sergey Sandimirov, Irina Elizarova, Maria Malysheva, Dmitriy Makarov and Nikolay Kaganovich
Minerals 2025, 15(9), 973; https://doi.org/10.3390/min15090973 (registering DOI) - 14 Sep 2025
Abstract
The chemical composition of bottom sediments in the northern part of Lake Umbozero, located in close proximity to a closed rare metal mine in the Murmansk Region, was studied. This study is a continuation of our research into the impact of closed rare [...] Read more.
The chemical composition of bottom sediments in the northern part of Lake Umbozero, located in close proximity to a closed rare metal mine in the Murmansk Region, was studied. This study is a continuation of our research into the impact of closed rare metal mines and tailings on the environment. Samples were collected using an open gravity sampler in two sections of the lake in three replicates. The content of rare earth elements was determined using inductively coupled plasma mass spectrometry. The total content of elements was determined both in the surface layers of bottom sediments and in the deep layers that were formed in the preindustrial period and, thus, characterize the geochemical background of the study area. The average ∑REE in the surface layers of bottom sediments of Lake Umbozero in the wastewater reception area (Site 1) reaches 774 mg/kg, while for the area located north of the discharge site (Site 2), ∑REE was 208 mg/kg. The enrichment factor (EF), the geoaccumulation index (Igeo), the coefficient of the index of potential ecological risk (Eir) and the index of potential ecological hazard (RI) were calculated. Assessing the total pollution of bottom sediments of Lake Umbozero with rare earth elements, the value of potential ecological risk reaches values corresponding to the level of low and moderate ecological risk of pollution (RISite 1 = 164; RISite 2 = 104). The conducted correlation analysis allowed us to establish the main phases containing rare earth elements in the bottom sediments of Lake Umbozero—oxyhydroxide complex compounds with iron and manganese. Full article
Show Figures

Figure 1

21 pages, 3304 KB  
Article
The Average Structure of a Fine-Grained Nepheline to 900 °C: Disorder of O1, Al-Si, and K-Vacancy
by Sytle M. Antao
Minerals 2025, 15(9), 972; https://doi.org/10.3390/min15090972 (registering DOI) - 13 Sep 2025
Viewed by 84
Abstract
A fine-grained nepheline sample from Egan Chutes, Ontario, with the chemical composition (K1.320.68)(Na6.05Ca0.22)[Al7.77Si8.21O32], where ▯ represents vacancies, was studied through in situ synchrotron powder X-ray diffraction (XRD) data and [...] Read more.
A fine-grained nepheline sample from Egan Chutes, Ontario, with the chemical composition (K1.320.68)(Na6.05Ca0.22)[Al7.77Si8.21O32], where ▯ represents vacancies, was studied through in situ synchrotron powder X-ray diffraction (XRD) data and Rietveld structure refinement from 26 to 900 °C on heating and cooling. The average structure was refined in the space group P63. The satellite reflections in nepheline give rise to order–disorder transitions. The average <Al,Si-O>{4} distances in nepheline indicate a partially ordered Al-Si distribution, especially in the Al2 and Si2 sites at room T before heating. The nepheline structure shows that except for the positional disorder of the O1 oxygen atom, the other atoms are well defined and contain no unusual features. Vacancies, ▯, occur at the K site. Different satellite (s) reflections arise from (1) positional order of the O1 atoms to 299 °C (s1 disappears), (2) K-▯ order to 486 °C (s2 and s3 disappear), and (3) some Al-Si order 900 °C, where some satellite reflections are present. Complete Al-Si order is obtained at room T on cooling. Full article
Show Figures

Figure 1

41 pages, 5058 KB  
Review
Review of Enargite Flotation—Part I: Surface Characterization and Advances in Selective Flotation
by Pablo Miranda-Villagrán, Rodrigo Yepsen, Andrés Ramírez-Madrid, Jorge H. Saavedra and Leopoldo Gutiérrez
Minerals 2025, 15(9), 971; https://doi.org/10.3390/min15090971 (registering DOI) - 13 Sep 2025
Viewed by 137
Abstract
Enargite (Cu3AsS4), a copper–arsenic sulfosalt, represents a critical challenge in copper mineral processing due to its high arsenic content, which poses significant environmental, metallurgical, and economic issues. Its flotation behavior closely resembles that of other copper sulfides such as [...] Read more.
Enargite (Cu3AsS4), a copper–arsenic sulfosalt, represents a critical challenge in copper mineral processing due to its high arsenic content, which poses significant environmental, metallurgical, and economic issues. Its flotation behavior closely resembles that of other copper sulfides such as chalcopyrite and chalcocite, complicating selective separation at early beneficiation stages. This review presents a comprehensive examination of enargite’s surface chemistry and electrochemical behavior, focusing on the influence of oxidation, pH, and pulp potential on surface reactivity, charge distribution (zeta potential), and hydrophobicity. Detailed insights into the formation of surface oxidation layers, passivation mechanisms, and contact angle variations are provided to elucidate collector-mineral interactions. Advances in selective flotation techniques are also discussed, including the use of depressant reagents, controlled redox environments, and reagent conditioning strategies. Special attention is given to flotation in seawater, where ionic strength and multivalent ions significantly influence mineral-reagent interactions and flotation outcomes. Galvanic interactions between enargite and other sulfide minerals are identified as critical factors affecting floatability and selectivity. The review consolidates findings from recent experimental and electrochemical studies, highlighting promising approaches to enhance enargite rejection and copper concentrate purity. It concludes with perspectives on future research aimed at optimizing flotation processes and developing sustainable solutions for processing arsenic-bearing copper ores. Full article
Show Figures

Figure 1

19 pages, 3745 KB  
Article
Anomaly Detection in Mineral Micro-X-Ray Fluorescence Spectroscopy Based on a Multi-Scale Feature Aggregation Network
by Yangxin Lu, Weiming Jiang, Molei Zhao, Yuanzhi Zhou, Jie Yang, Kunfeng Qiu and Qiuming Cheng
Minerals 2025, 15(9), 970; https://doi.org/10.3390/min15090970 (registering DOI) - 13 Sep 2025
Viewed by 89
Abstract
Micro-X-ray fluorescence spectroscopy (micro-XRF) integrates spatial and spectral information and is widely employed for multi-elemental analyses of rock-forming minerals. However, its inherent limitation in spatial resolution gives rise to significant pixel mixing, thereby hindering the accurate identification of fine-scale or anomalous mineral phases. [...] Read more.
Micro-X-ray fluorescence spectroscopy (micro-XRF) integrates spatial and spectral information and is widely employed for multi-elemental analyses of rock-forming minerals. However, its inherent limitation in spatial resolution gives rise to significant pixel mixing, thereby hindering the accurate identification of fine-scale or anomalous mineral phases. Furthermore, most existing methods heavily rely on manually labeled data or predefined spectral libraries, rendering them poorly adaptable to complex and variable mineral systems. To address these challenges, this paper presents an unsupervised deep aggregation network (MSFA-Net) for micro-XRF imagery, aiming to eliminate the reliance of traditional methods on prior knowledge and enhance the recognition capability of rare mineral anomalies. Built on an autoencoder architecture, MSFA-Net incorporates a multi-scale orthogonal attention module to strengthen spectral–spatial feature fusion and employs density-based adaptive clustering to guide semantically aware reconstruction, thus achieving high-precision responses to potential anomalous regions. Experiments on real-world micro-XRF datasets demonstrate that MSFA-Net not only outperforms mainstream anomaly detection methods but also transcends the physical resolution limits of the instrument, successfully identifying subtle mineral anomalies that traditional approaches fail to detect. This method presents a novel paradigm for high-throughput and weakly supervised interpretation of complex geological images. Full article
(This article belongs to the Special Issue Gold–Polymetallic Deposits in Convergent Margins)
Show Figures

Figure 1

25 pages, 863 KB  
Review
Clay Minerals as Enzyme Carriers for Pollutant Removal from Wastewater: A Comprehensive Review
by Naima Sayahi, Bouthaina Othmani, Wissem Mnif, Zaina Algarni, Moncef Khadhraoui and Faouzi Ben Rebah
Minerals 2025, 15(9), 969; https://doi.org/10.3390/min15090969 (registering DOI) - 13 Sep 2025
Viewed by 129
Abstract
Water pollution continues to pose a critical global challenge, largely due to the unregulated discharge of industrial, agricultural, and municipal effluents. Among emerging solutions, enzymatic bioremediation stands out as a sustainable and environmentally friendly approach, offering high specificity and efficiency under mild conditions. [...] Read more.
Water pollution continues to pose a critical global challenge, largely due to the unregulated discharge of industrial, agricultural, and municipal effluents. Among emerging solutions, enzymatic bioremediation stands out as a sustainable and environmentally friendly approach, offering high specificity and efficiency under mild conditions. Nonetheless, the practical application of free enzymes is hindered by their inherent instability, poor reusability, and susceptibility to denaturation. To address these limitations, the immobilization of enzymes onto solid supports, particularly clay minerals, has garnered increasing attention. This review presents a detailed analysis of clay minerals as promising carriers for enzyme immobilization in wastewater treatment. It explores their classification, structural characteristics, and physicochemical properties, highlighting key advantages such as a large surface area, cation exchange capacity, and thermal stability. Functionalization techniques, including acid/base activation, intercalation, grafting, and pillaring, are discussed in terms of improving enzyme compatibility and catalytic performance. Various immobilization methods such as physical adsorption, covalent bonding, entrapment, crosslinking, and intercalation are critically evaluated with regard to enhancing enzyme activity, stability, and recyclability. Recent case studies demonstrate the effective removal of pollutants such as dyes, pharmaceuticals, and heavy metals using enzyme–clay composites. Despite these advances, challenges such as enzyme leaching, mass transfer resistance, and variability in clay composition persist. This review concludes by outlining future prospects, including the development of hybrid and magnetic clay-based systems and their integration into advanced water treatment technologies. Overall, enzyme immobilization on clay minerals represents a promising and scalable approach for the next generation of wastewater bioremediation strategies. Full article
Show Figures

Figure 1

15 pages, 5846 KB  
Article
The Effect of Ore Pre-Heating on the Operation of a 300 kVA Submerged Arc Furnace for High Carbon Ferromanganese Alloy Production—Pilot Study Results
by Matale Samuel Moholwa, Sello Peter Tsebe, Derek Hayman, Sanda Moloane, Joalet Steenkamp, Martin Sitefane and Driaan Bezuidenhout
Minerals 2025, 15(9), 968; https://doi.org/10.3390/min15090968 (registering DOI) - 13 Sep 2025
Viewed by 96
Abstract
The effect of ore pre-heating on the operation of a 300 kVA Submerged Arc Furnace (SAF) for high carbon ferromanganese (HCFeMn) alloy was investigated. The two types of Mn ores from the Kalahari Manganese Field (KMF) were used in the investigation (Ore #1 [...] Read more.
The effect of ore pre-heating on the operation of a 300 kVA Submerged Arc Furnace (SAF) for high carbon ferromanganese (HCFeMn) alloy was investigated. The two types of Mn ores from the Kalahari Manganese Field (KMF) were used in the investigation (Ore #1 and Ore #2). Quartz and coke sourced from South Africa were used as a fluxing agent and a reductant, respectively. The Mn ores, reductant and fluxing agent were delivered to Mintek with a size range of +6–20 mm and were sent to our in-house laboratories to determine the chemical and physical properties. The samples were taken for Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES), combustion method (LECO), proximate analysis and quantitative X-ray diffraction (QXRD). A newly designed and constructed pilot facility at Mintek was used in the investigation. The facility included a 1 t/h rotary kiln coupled to an electric arc furnace supplied with an alternating current (AC) with a 300 kVA tap-changer transformer. The main aim of the investigation was to demonstrate the effect of ore pre-heating to 600 °C on the furnace energy consumption and CO/CO2 emissions. The experimental approach adopted involved feeding Mn ore to establish baseline operating conditions, followed by feeding of Mn ore pre-heated with a rotary kiln to compare operational parameters. The pilot campaign experienced several operational challenges but there were periods of stable operation that enabled data collection for furnace energy consumption and CO/CO2 emissions. The effect of pre-heating the ore to 600 °C on the SAF energy consumption and CO/CO2 emissions was demonstrated successfully and revealed that energy savings and reduction in furnace CO2 emissions is achievable. Pre-heating Mn ore to 600 °C lowered the furnace energy consumption by an average of 22.5% and CO2 emissions by an average of 37%. The campaign also achieved an overall manganese recovery of 86%. Operating the furnace with hot feed increased the heat losses through the roof by 300% compared to heat losses observed during cold feed. There were also no significant changes in the furnace electrical parameters observed between the two feed modes. Full article
(This article belongs to the Section Mineral Processing and Extractive Metallurgy)
Show Figures

Figure 1

20 pages, 18970 KB  
Article
Process Mineralogy Study and Flotation Testwork of a Complex Lead–Gold Rougher Concentrate
by Guomin Chen, Han Zhao, Joe Zhou, Zilong Liu and Hongying Yang
Minerals 2025, 15(9), 967; https://doi.org/10.3390/min15090967 - 12 Sep 2025
Viewed by 125
Abstract
A lead–gold rougher concentrate was studied to investigate the efficiency of mineral processing. Using process mineralogy as the guiding theory, mineralogical parameters such as chemical composition, mineral composition, mineral particle size, and symbiotic association between minerals were studied in detail. A systematic lead [...] Read more.
A lead–gold rougher concentrate was studied to investigate the efficiency of mineral processing. Using process mineralogy as the guiding theory, mineralogical parameters such as chemical composition, mineral composition, mineral particle size, and symbiotic association between minerals were studied in detail. A systematic lead flotation testwork program was carried out to obtain the optimal flotation and separation conditions, and the products obtained were analyzed. The results show that the concentrate contains a wide variety of minerals with complex material composition, and the lead mineral was mainly galena with a relative content of 3.43% and a particle size −37 μm accounting for 94.72%, while the gold minerals were dominated by electrum. The grades of gold, silver, and lead in the balland obtained through the flotation closed-circuit test were 512.10 g/t, 1632.80 g/t, and 40.38%, and the recoveries were 70.65%, 73.86%, and 75.37%, respectively. The gold lost in the flotation tailings was mainly dominated by gold encapsulated in metal sulfide (accounting for 55.67%), and the lead lost was mainly in gangue and metal oxides (accounting for 62.72%). Full article
(This article belongs to the Section Mineral Processing and Extractive Metallurgy)
Show Figures

Figure 1

17 pages, 7660 KB  
Article
Subresolution Porosity Estimation of Porous Rocks from CT Images: Incorporating X-Ray Mass Attenuation Coefficients
by Jianhuang Chen, Zhongjian Zhang, Zhenyu Long, Qiong Zhang and Zhongqi Yue
Minerals 2025, 15(9), 966; https://doi.org/10.3390/min15090966 - 12 Sep 2025
Viewed by 101
Abstract
Rock porosity is a key parameter for quantifying fluid flow properties and predicting mechanical behaviour. Although X-ray CT imaging has been widely used to estimate porosity, the accuracy of such methods is still hindered by beam energy and mineralogical heterogeneity. In this study, [...] Read more.
Rock porosity is a key parameter for quantifying fluid flow properties and predicting mechanical behaviour. Although X-ray CT imaging has been widely used to estimate porosity, the accuracy of such methods is still hindered by beam energy and mineralogical heterogeneity. In this study, a methodology for the estimation of subresolution porosity is proposed, taking into account the relative relationship of X-ray mass attenuation coefficients (MACs) among minerals. The approach segments macroparticles, matrix, and macropores and calibrates their relative X-ray MAC relationships to establish the upper and lower bounds of the matrix LAC. Subresolution porosity is then estimated based on these calibrated limits. Taking Belgian Fieldstone and Bentheimer Sandstone as examples, the method described in this paper has stronger connectivity than does the binarised porosity estimation method and higher estimation accuracy than does the subresolution porosity calculation method, which does not consider the MAC. The proposed method is intended to refine the rationality of the subresolution porosity calculation and to broaden its theoretical scope of application. Full article
(This article belongs to the Section Clays and Engineered Mineral Materials)
Show Figures

Figure 1

28 pages, 4033 KB  
Article
Assessing Jarosite Kinetic Dissolution Rates at Acidic Conditions and Different Temperatures
by Mateus De Souza Buriti, Marie Poulain, Pierre Cézac and Lidia Casás
Minerals 2025, 15(9), 965; https://doi.org/10.3390/min15090965 - 11 Sep 2025
Viewed by 175
Abstract
K-jarosite (KFe3(SO4)2(OH)6), the most common jarosite-type mineral in natural and industrial settings, has been widely studied to understand its dissolution behavior in both environmental and industrial contexts. However, reported kinetic data remain inconsistent due to [...] Read more.
K-jarosite (KFe3(SO4)2(OH)6), the most common jarosite-type mineral in natural and industrial settings, has been widely studied to understand its dissolution behavior in both environmental and industrial contexts. However, reported kinetic data remain inconsistent due to the combined influence of kinetic factors, despite the importance of such data for optimizing system conditions and improving process control and environmental management. The present work aims to help elucidate K-jarosite dissolution by carrying out new experiments in sulfuric acid medium (pH 1 and 2) at different temperatures (296, 323 and 343 K) and using two initial concentrations (0.4 and 1 g of K-jarosite/kg of solution). K-jarosite was synthesized and characterized by analytical techniques (XRD, SEM and BET), and the composition was determined by induction-coupled plasma optical emission spectroscopy (ICP-OES). Derivative (DVKM), Noyes–Whitney (NWKM) and Shrinking Core (SCKM) kinetic models previously used in the literature of jarosite-type compounds were adjusted to the data obtained here and compared. The results showed that higher temperatures and lower pH led to faster dissolution rates. Smaller initial concentrations decreased the rates slightly but had less impact than the other variables. Experiments at pH 1 led to the dissolution of all jarosite solids, while at pH 2 they led to incomplete dissolution. Remarkably, at pH 2 and at higher temperatures (mainly at 343 K), there was slight reprecipitation of the iron. XRD analysis identified no peak other than K-jarosite peaks after dissolution. DVKM and NWKM represented the effect of the studied parameters well. However, only using SCKM was a kinetic equation describing the dissolution process obtained. While the behavior of the kinetic curve is well established, the model fails to correctly describe the induction period. Under extreme conditions (>323 K, pH 1), dissolution is described by a chemical reaction controlling stage and it changes to mass transport in mild conditions. As theoretically expected, the results obtained in this work give important information about the prediction of the behavior of jarosite dissolution in terrestrial environments (acid mine and acid rock drainages) and hydrometallurgical process in mild acidic conditions and high temperatures. Full article
(This article belongs to the Section Environmental Mineralogy and Biogeochemistry)
Show Figures

Figure 1

21 pages, 3293 KB  
Article
Initial Characterization of Titanium and Vanadium-Rich Magnetite from the Manastir Heights in Southeast Bulgaria Aiming at Future Environmentally Friendly Beneficiation
by Marinela Panayotova, Ivan Dimitrov and Angelika Sofronieva
Minerals 2025, 15(9), 964; https://doi.org/10.3390/min15090964 - 11 Sep 2025
Viewed by 83
Abstract
Titanium (Ti) and vanadium (V) are metals critical for the sustainable development of our society. Their growing demand and the depletion of ores rich in these metals along with technological development lead to a reconsideration of sources that were previously considered unpromising. The [...] Read more.
Titanium (Ti) and vanadium (V) are metals critical for the sustainable development of our society. Their growing demand and the depletion of ores rich in these metals along with technological development lead to a reconsideration of sources that were previously considered unpromising. The present work is devoted to the study of an iron (Fe) ore from southeastern Bulgaria, containing Ti and V in low but potentially recoverable concentrations. The aim was to check whether it is possible to obtain an iron concentrate containing Ti and V in concentrations comparable to those in similar market products. The material was examined by optical microscopy, XRD, SEM-EDS, and ICP MS. Magnetic separation was applied with and without predating gravity separation. By applying wet gravity beneficiation followed by a low-intensity magnetic field, an iron concentrate (40%–65% Fe) bearing 3%–5% Ti and 0.4%–0.59% V was obtained. Using only a low-intensity magnetic field, without gravity separation, an iron concentrate (59.4% Fe) containing 3.5% Ti and 0.44% V was obtained. Vanadium was extracted in the highly magnetic material, while a significant amount of Ti was left in the weak magnetic fraction. An additional 1.5% may be recovered by applying a high-intensity magnetic field. The main processing challenge appears to be the recovery, without flotation beneficiation, of magnetite that is oxidized to non-magnetic hematite and maghemite. Using magnetic separation (with or without preliminary wet gravity beneficiation) avoids pollution of the processing waste with reagents. Thus, the waste from the beneficiation of the studied type of ore can be used as a soil improver. As a result, the extraction of critical metals using a practically waste-free technology may be achieved. Full article
Show Figures

Figure 1

20 pages, 9171 KB  
Article
New Insights into Chromogenic Mechanism and the Genesis of Blue Jadeite from Guatemala
by Yining Liu, Bo Xu, Siyi Zhao, Mengxi Zhao, Zitong Li and Wenxin Hao
Minerals 2025, 15(9), 963; https://doi.org/10.3390/min15090963 - 11 Sep 2025
Viewed by 169
Abstract
While existing studies on Guatemalan jadeite have predominantly focused on green varieties, the coloration mechanisms and origin of its blue counterparts remain poorly understood. Therefore, the present study provides the first comprehensive investigation of the Guatemalan blue jadeite using an integrated analytical approach, [...] Read more.
While existing studies on Guatemalan jadeite have predominantly focused on green varieties, the coloration mechanisms and origin of its blue counterparts remain poorly understood. Therefore, the present study provides the first comprehensive investigation of the Guatemalan blue jadeite using an integrated analytical approach, which combines Raman spectroscopy, micro X-ray fluorescence (µ-XRF), electron microprobe analysis (EMPA), X-ray diffraction (XRD), UV-Vis spectroscopy, and Cathodoluminescence (CL) imaging on seven representative samples. The results demonstrate that these jadeites consist of two distinct phases: a primary jadeite phase (NaAlSi2O6) and a secondary omphacite that form by metasomatic alteration by Mg-Ca-Fe-rich fluids. Spectroscopic analysis reveals that the blue coloration is primarily controlled by Fe3+ electronic transitions (with characteristic absorption at 381 nm and 437 nm) coupled with Fe2+-Ti4+ intervalence charge transfer, supported by μ-XRF mapping showing strong Fe-Ti spatial correlation with color intensity. CL imaging documents a multi-stage formation history involving initial high-pressure crystallization (Jd-I) followed by fluid-assisted recrystallization forming Jd-II and omphacite. The detection of CH4, CO and H2O in the fluid inclusions by Raman spectroscopy indicates formation in a serpentinization-related reducing environment, while distinct CL zoning patterns confirm a fluid-directed crystallization (P-type) origin. These findings not only clarify the chromogenic processes and petrogenesis of Guatemalan blue jadeite but also establish key diagnostic criteria for its identification, advancing our understanding of fluid-derived jadeite formation in subduction zone environments. Full article
Show Figures

Figure 1

26 pages, 7402 KB  
Article
Hybrid Architecture for Tight Sandstone: Automated Mineral Identification and Quantitative Petrology
by Lanfang Dong, Chenxu Sun, Xiaolu Yu, Xinming Zhang, Menglian Chen and Mingyang Xu
Minerals 2025, 15(9), 962; https://doi.org/10.3390/min15090962 - 11 Sep 2025
Viewed by 85
Abstract
This study proposes an integrated computer vision system for automated petrological analysis of tight sandstone micro-structures. The system combines Zero-Shot Segmentation SAM (Segment Anything Model), Mask R-CNN (Region-Based Convolutional Neural Networks) instance segmentation, and an improved MetaFormer architecture with Cascaded Group Attention (CGA) [...] Read more.
This study proposes an integrated computer vision system for automated petrological analysis of tight sandstone micro-structures. The system combines Zero-Shot Segmentation SAM (Segment Anything Model), Mask R-CNN (Region-Based Convolutional Neural Networks) instance segmentation, and an improved MetaFormer architecture with Cascaded Group Attention (CGA) attention mechanism, together with a parameter analysis module to form a hybrid deep learning system. This enables end-to-end mineral identification and multi-scale structural quantification of granulometric properties, grain contact relationships, and pore networks. The system is validated on proprietary tight sandstone datasets, SMISD (Sandstone Microscopic Image Segmentation Dataset)/SMIRD (Sandstone Microscopic Image Recognition Dataset). It achieves 92.1% mIoU segmentation accuracy and 90.7% mineral recognition accuracy while reducing processing time from more than 30 min to less than 2 min per sample. The system provides standardized reservoir characterization through automated generation of quantitative reports (Excel), analytical images (JPG), and structured data (JSON), demonstrating production-ready efficiency for tight sandstone evaluation. Full article
(This article belongs to the Section Mineral Exploration Methods and Applications)
Show Figures

Figure 1

15 pages, 2807 KB  
Article
Investigation of the Coloration Mechanisms of Yellow-Green Nephrite from Ruoqiang (Xinjiang), China
by Boling Huang, Mingxing Yang, Xihan Yang, Xuan Wang, Ting Fang, Hongwei Han and Shoucheng Wang
Minerals 2025, 15(9), 961; https://doi.org/10.3390/min15090961 - 10 Sep 2025
Viewed by 183
Abstract
This study systematically investigates the color origin and coloration mechanisms of yellow-green nephrite from Ruoqiang, Xinjiang, using multiple analytical techniques including hyperspectral colorimetry, X-ray fluorescence (XRF) spectroscopy, titrimetry, laser ablation inductively coupled plasma–mass spectrometry (LA-ICP-MS), Raman spectroscopy and ultraviolet–visible (UV-Vis) spectroscopy. A pioneering [...] Read more.
This study systematically investigates the color origin and coloration mechanisms of yellow-green nephrite from Ruoqiang, Xinjiang, using multiple analytical techniques including hyperspectral colorimetry, X-ray fluorescence (XRF) spectroscopy, titrimetry, laser ablation inductively coupled plasma–mass spectrometry (LA-ICP-MS), Raman spectroscopy and ultraviolet–visible (UV-Vis) spectroscopy. A pioneering quantitative model (R2 = 0.942) was established between hue (H) and the Fe2O3 ratio (Fe2O3/TFe), revealing that the coloration mechanism is jointly governed by Fe3+ charge transfer (300–400 nm absorption band) and Fe2+→Fe3+ transitions (600–630 nm absorption band). Furthermore, the intensity variation in the 3651 cm−1 Raman peak serves to further confirm the critical role of Fe3+ occupancy in the tremolite lattice for color modulation. In combination with the partition patterns of Rare Earth elements (REEs) (right-leaning LREE distribution with negative Eu anomaly) and trace element characteristics, this study supports the classification of Ruoqiang yellow-green nephrite as a high oxygen fugacity magnesian marble-type deposit. In this type of deposit, the ore-forming environment facilitates Fe3+ enrichment and yellow-green hue formation. The findings provide new theoretical insights into the chromatic genesis of yellow-green nephrite and hold significant implications for its identification, quality grading, and research on metallogenic mechanisms. Full article
Show Figures

Figure 1

16 pages, 2262 KB  
Article
Geochemistry and Th–U–Total Pb Chemical Ages of Late Variscan Uranium Mineralisation at Shkhara, Greater Caucasus
by Franziska D. H. Wilke, Avtandil Okrostsvaridze, David Bluashvili and Rabi Gabrielashvili
Minerals 2025, 15(9), 960; https://doi.org/10.3390/min15090960 - 9 Sep 2025
Viewed by 213
Abstract
We present the chemical composition and the U-Pb chemical age of the recently discovered uranium mineralisation occurrence in the crystalline Shkhara Massif in the Greater Caucasus. The mineralisation consists of hydrothermal uraninites from veins that intersect into the Late Variscan biotite–plagioclase-rich granite and [...] Read more.
We present the chemical composition and the U-Pb chemical age of the recently discovered uranium mineralisation occurrence in the crystalline Shkhara Massif in the Greater Caucasus. The mineralisation consists of hydrothermal uraninites from veins that intersect into the Late Variscan biotite–plagioclase-rich granite and migmatites. The chemical composition and the Th–U total Pb chemical age of the uraninites were determined. Results show thorium-rich, (∑LREE/∑HREE)N unfractionated uraninites that had been formed under higher temperatures above 450 ± 50 °C. Fifty-eight measurements on 14 grains revealed homogeneous and unaltered uraninites. Th–U–total Pb ages of the uraninite were calculated from 55 chemical analyses, among which 37 plot between 275 and 305 Ma. The weighted median age of the 55 data points corresponds to 291 ± 14 Ma: the boundary between the Carboniferous and Permian periods. These dates suggest that uraninite mineralisation is related to the late orogenic extensional process of the Great Caucasus structure. During this process, hydrothermal fluids permeated the biotite-+ and plagioclase-rich magmatic rocks of the Main Range zone and formed U- and Th-rich veins and uraninite mineralisation. This study shows that the Shkhara uranium occurrence correlates with most of the late Variscan uranium deposits in Central and Western Europe in terms of geodynamic setting, composition, age and type of mineralisation. Full article
(This article belongs to the Special Issue Advances in Uranium Metallogenic Theory, Exploration and Exploitation)
Show Figures

Graphical abstract

16 pages, 3535 KB  
Article
Flotation Behavior and Mechanism of Andalusite and Quartz Under the Sodium Dodecyl Sulfonate System
by Liqiang Lin, Guanfei Zhao, Tingsheng Qiu, Chong Deng, Wenhui Yang and Xiaowen Zhou
Minerals 2025, 15(9), 959; https://doi.org/10.3390/min15090959 - 9 Sep 2025
Viewed by 456
Abstract
The paper systematically investigated the flotation behavior and interaction mechanisms of andalusite and quartz under sodium dodecyl sulfonate (SDS) through integrated experimental and computational approaches, including zeta potential measurements, Fourier-transform infrared (FTIR) spectroscopy, Materials Studio (MS)-based quantum chemical calculations, and single-mineral flotation tests. [...] Read more.
The paper systematically investigated the flotation behavior and interaction mechanisms of andalusite and quartz under sodium dodecyl sulfonate (SDS) through integrated experimental and computational approaches, including zeta potential measurements, Fourier-transform infrared (FTIR) spectroscopy, Materials Studio (MS)-based quantum chemical calculations, and single-mineral flotation tests. The results of zeta potential and infrared spectroscopy analysis indicated that SDS underwent strong chemical adsorption on the surface of andalusite, while the adsorption effect on the surface of quartz was not obvious. MS calculations showed that the {100} surface energy of andalusite was the lowest, and it was the most important dissociation surface. After SDS was adsorbed on the {100} surface of andalusite, the aluminum atoms on the surface of andalusite lost electrons, resulting in a significant increase in the number of positive charges they carried. The activity of oxygen atoms was enhanced, while the number of charges carried by silicon atoms changed relatively little. It was indicated that SDS adsorbed the active sites of Al atoms on the surface of andalusite. The results of the pure mineral flotation test further verified the accuracy of the previous test results, indicating that andalusite and quartz had a good flotation separation effect under the SDS system. Full article
(This article belongs to the Special Issue Harnessing Surface Chemistry for Enhanced Mineral Recovery)
Show Figures

Figure 1

10 pages, 790 KB  
Article
An Integrated Separation Approach for Beneficiation of Low-Grade Iron Ore
by Mahdi Ostadrahimi, Saeed Farrokhpay, Tooraj Zare, Mohammad Aghajanlou, Khodakaram Gharibi and Mohammad Mahdi Salari Rad
Minerals 2025, 15(9), 958; https://doi.org/10.3390/min15090958 - 8 Sep 2025
Viewed by 279
Abstract
Iron ore beneficiation is crucial for sustainable utilization of low-grade iron ores. Conventional separation methods often fail to efficiently upgrade the iron ores containing complex mineral phases, such as hematite, goethite, ankerite, and limonite. This study evaluated an integrated roasting–leaching–magnetic separation approach applied [...] Read more.
Iron ore beneficiation is crucial for sustainable utilization of low-grade iron ores. Conventional separation methods often fail to efficiently upgrade the iron ores containing complex mineral phases, such as hematite, goethite, ankerite, and limonite. This study evaluated an integrated roasting–leaching–magnetic separation approach applied to an iron ore. Roasting at 800 °C for 90 min significantly enhanced the Fe(II) content and improved magnetic susceptibility, facilitating superior iron-containing minerals separation efficiency. Furthermore, sulfuric acid leaching effectively eliminated non-magnetic impurities such as calcite, improving iron recovery. Davis tube recovery experiments confirmed that this combination markedly enhanced weight recovery (Rw) and iron recovery (Rg), outperforming traditional methods. The findings highlight the synergistic effect of roasting and leaching for refining iron ores and propose an optimized beneficiation strategy. This approach offers an effective method for processing complex iron ores, particularly those with low Fe grade and challenging impurities, improving beneficiation efficiency and mineral extraction. Full article
Show Figures

Figure 1

15 pages, 2876 KB  
Review
Permanent Cathode Technologies in Copper Electrowinning: Development and Status
by Kalin Naidoo and Kathryn C. Sole
Minerals 2025, 15(9), 957; https://doi.org/10.3390/min15090957 - 8 Sep 2025
Viewed by 293
Abstract
The replacement of copper metal starter-sheet cathodes with the use of permanent cathode technology, in which the target metal is plated onto an inert blank template, has enabled significant benefits in the copper electrowinning process. These include the application of significantly higher current [...] Read more.
The replacement of copper metal starter-sheet cathodes with the use of permanent cathode technology, in which the target metal is plated onto an inert blank template, has enabled significant benefits in the copper electrowinning process. These include the application of significantly higher current density, which reduces tankhouse footprint and increases process intensity per unit area; improved operator safety with less reliance on manual electrode handling; and the implementation of process automation and robotics. Cathodes of >99.99% chemical purity and with a smooth and aesthetic surface morphology are consistently produced. This review considers the evolution and development of the permanent cathode process, its commercial adoption across the global copper industry, and the current technology status. Full article
Show Figures

Figure 1

21 pages, 15357 KB  
Article
The Fluid Evolution and Metallogenic Processes of the Liba Gold Deposit, West Qinling, China: Insights from the Texture, Trace Elements, and H-O Isotope Geochemistry of Quartz
by Yu Chen, Yuwang Wang, Jianping Wang, Dedong Li, Jian Geng, Jianxiang Luo and Rui Wang
Minerals 2025, 15(9), 956; https://doi.org/10.3390/min15090956 - 8 Sep 2025
Viewed by 268
Abstract
The evolution of ore-forming fluids in gold precipitation is a key aspect in understanding the genesis of orogenic gold deposits. Traditional fluid inclusion analyses are often limited in revealing the fluid property changes during mineralization, leading to significant debates on the mineralization temperature [...] Read more.
The evolution of ore-forming fluids in gold precipitation is a key aspect in understanding the genesis of orogenic gold deposits. Traditional fluid inclusion analyses are often limited in revealing the fluid property changes during mineralization, leading to significant debates on the mineralization temperature and fluid sources. In this study, we selected the Liba gold deposit in the West Qinling orogen and employed scanning electron microscope–cathodoluminescence (SEM-CL) and laser ablation–inductively coupled plasma mass spectrometry (LA-ICPMS) to analyze the microstructure and trace element characteristics of quartz veins, revealing the multi-stage evolution of ore-forming fluids and the mineralization mechanisms. SEM-CL imaging identified five distinct quartz stages. The pre-mineralization (Qz0) and early-stage mineralization (Qz1) fluids were predominantly magmatic–metamorphic in origin, as indicated by relatively high δ18O and δD values. During the primary metallogenic (Qz2a, Qz2b) and late-stage mineralization (Qz3), temperatures progressively decreased, and the gradual mixing of meteoric water and formation water was observed, which promoted gold precipitation. And the content of trace elements in post-mineralization quartz (Qz4) is significantly lower and similar to that in the Qz0 stage. Through the analysis of quartz trace elements (e.g., Al/Ti, Ge/Al ratios) and isotope data (δ18O = 8.25‰ to 12.67‰, δD = −119.1‰ to −79.8‰), the results indicate that the Liba gold deposit is a medium- to low-temperature orogenic gold deposit. Furthermore, the gold enrichment process was primarily driven by a hydrothermal system, with variations in the fluid composition during mineralization contributing to the concentration of gold. Full article
(This article belongs to the Section Mineral Deposits)
Show Figures

Figure 1

27 pages, 3247 KB  
Article
Impact of Historical Mining and Metallurgical Technologies on Soil and Sediment Composition Along the Ibar River
by Robert Šajn, Jasminka Alijagić and Trajče Stafilov
Minerals 2025, 15(9), 955; https://doi.org/10.3390/min15090955 - 6 Sep 2025
Viewed by 340
Abstract
This study systematically investigates soil and stream sediment along the 165 km Ibar River to examine the origin and transfer of pollutants. The research focuses on the environmental impact of long-term mining and irregular waste management, as well as natural enrichment related to [...] Read more.
This study systematically investigates soil and stream sediment along the 165 km Ibar River to examine the origin and transfer of pollutants. The research focuses on the environmental impact of long-term mining and irregular waste management, as well as natural enrichment related to weathering processes. A comprehensive sampling campaign was conducted, collecting 70 samples from 14 locations. At each location, samples of river sediment, floodplain soil (0–5 cm and 20–30 cm depths), and river terrace soil (same depths) were collected. The contents of 21 elements (Ag, Al, As, B, Ba, Ca, Cd, Cr, Cu, Fe, K, Li, Mg, Mn, Na, Ni, P, Pb, Sr, V, and Zn) were determined using inductively coupled plasma atomic emission spectrometry (ICP-AES). Analysis of Variance (ANOVA) was performed to identify statistically significant differences in element contents between defined zones, sampled materials (river sediments, floodplain soils, and river terrace soils), and sampled soil horizons (topsoil, 0–5 cm, and subsoil, 20–30 cm). Multivariate analysis, including correlation coefficient, cluster analysis, and principal component analysis, revealed two distinct groups of elements with highly significant correlation coefficients (r > 0.7). The first group, comprising Ag, As, Cd, Cu, Mn, and Zn, indicates anthropogenic enrichment, likely resulting from mining and smelting activities in the middle flow of the Ibar River (The Mining and Metallurgical Complex Trepča). The second group, consisting of Cr, Mg, and Ni, suggests enrichment related to the weathering of elements from the ophiolite zone in the lower Ibar River. The study found high enrichment ratios of toxic elements like arsenic, cadmium, lead, and zinc, particularly in stream sediments and floodplains. Notably, arsenic contents exceeded European averages by up to 57 times in stream sediments, posing a significant environmental concern due to its high content. Full article
(This article belongs to the Special Issue Mineralogy and Geochemistry of Sediments)
Show Figures

Figure 1

16 pages, 2834 KB  
Article
The Effect of Particle Size and Dodecylamine Concentration on the Flotation of Lepidolite in Alkaline Medium
by Martín Reyes Pérez, Francisco Patiño Cardona, Hernan Islas Vázquez, Iván Alejandro Reyes Domínguez, Mizraim Uriel Flores Guerrero, Miguel Pérez Labra, Julio Cesar Juárez Tapia, Dayli Yamileth Tolentino Mendoza and Miroslava Mishelle Sánchez Acosta
Minerals 2025, 15(9), 954; https://doi.org/10.3390/min15090954 - 6 Sep 2025
Viewed by 424
Abstract
Currently, lepidolite is considered an important natural alternative for obtaining lithium, given the difficulty in processing other species containing this metal. However, its mechanical preparation and beneficiation present considerable challenges and play a critical role in its efficient separation by flotation. This study [...] Read more.
Currently, lepidolite is considered an important natural alternative for obtaining lithium, given the difficulty in processing other species containing this metal. However, its mechanical preparation and beneficiation present considerable challenges and play a critical role in its efficient separation by flotation. This study explores the effect of particle size and dodecylamine concentration during flotation in a laboratory Denver cell. The results indicate that particle size significantly affects the finding in which the optimum was −90 + 75 μm, with a separation efficiency of 94%, and with only 2.067 × 10−5 M of dodecylamine (DDA) (5 g/t) at pH 11.0. The hydrophobicity of lepidolite was generated by the effect of the chemisorption of the cationic collector and the FTIR results indicate detection of the characteristic bands of the adsorption of DDA to the surface of lepidolite. Full article
(This article belongs to the Special Issue Surface Chemistry and Reagents in Flotation)
Show Figures

Figure 1

18 pages, 4459 KB  
Article
Geochemical Constraints on Antimony Mineralization in the Gutaishan Au–Sb Deposit, China: Insights from Trace Elements in Quartz and Sulfur Isotopes in Stibnite
by Jingping Feng, Linyan Kang, Bin Li and Peixuan Kang
Minerals 2025, 15(9), 953; https://doi.org/10.3390/min15090953 - 6 Sep 2025
Viewed by 329
Abstract
The Gutaishan Au–Sb deposit is situated in the southern segment of the Jiangnan Orogenic Belt, a region characterized by a concentration of Au–Sb–W deposits. Previous research has predominantly concentrated on Au mineralization, whereas studies addressing the equally important Sb mineralization are relatively scarce. [...] Read more.
The Gutaishan Au–Sb deposit is situated in the southern segment of the Jiangnan Orogenic Belt, a region characterized by a concentration of Au–Sb–W deposits. Previous research has predominantly concentrated on Au mineralization, whereas studies addressing the equally important Sb mineralization are relatively scarce. To investigate key scientific questions regarding the source of ore-forming materials, the physicochemical conditions, and mineralization mechanisms of Sb in the Gutaishan deposit, we conducted systematic analyses of trace elements in hydrothermal quartz and sulfur isotopes in stibnite. Li, Al, Sb, B, Na, K, Ti, Ge, and As are the dominant trace elements in hydrothermal quartz from the Gutaishan deposit. The dominant substitution mechanism is (Al3+, Sb3+) + (Li+, Na+, K+, H+) ↔ Si4+. The relatively low but variable Al concentrations indicate that quartz precipitated from fluids with fluctuating pH and weakly acidic conditions, while variations in Ti and Ge reflect significant temperature changes. These features suggest that fluid mixing was the primary mineralization mechanism in the Gutaishan deposit. Hydrothermal quartz contains anomalously high B concentrations (14.36–30.64 ppm), far exceeding typical hydrothermal levels, while stibnite displays consistent magmatic sulfur isotope signatures (−3.50‰ to −4.2‰, with an average of −3.99 ± 0.2‰), which are markedly different from the in situ δ34S values of sedimentary sulfides (+7.0‰ to +23.3‰) in the host rocks. This combination of evidence indicates a magmatic–hydrothermal origin for Sb mineralization. Integrating previous geochronological and isotopic constraints with our new observations, we interpret that the Gutaishan deposit represents an intrusion-related Au–Sb deposit formed in a post-collisional extensional setting, where Sb was precipitated after Au mineralization as a result of fluid mixing. Full article
(This article belongs to the Section Mineral Deposits)
Show Figures

Figure 1

25 pages, 1812 KB  
Article
YOLO-EDH: An Enhanced Ore Detection Algorithm
by Lei Wan, Xueyu Huang and Zeyang Qiu
Minerals 2025, 15(9), 952; https://doi.org/10.3390/min15090952 - 5 Sep 2025
Viewed by 298
Abstract
Mineral identification technology is a key technology in the construction of intelligent mines. In ore classification and detection, mining scenarios present challenges, such as diverse ore types, significant scale variations, and complex surface textures. Traditional detection models often suffer from insufficient multi-scale feature [...] Read more.
Mineral identification technology is a key technology in the construction of intelligent mines. In ore classification and detection, mining scenarios present challenges, such as diverse ore types, significant scale variations, and complex surface textures. Traditional detection models often suffer from insufficient multi-scale feature representation and weak dynamic adaptability, leading to the missed detection of small targets and misclassification of similar minerals. To address these issues, this paper proposes an efficient multi-scale ore classification and detection model, YOLO-EDH. To begin, standard convolution is replaced with deformable convolution, which efficiently captures irregular defect patterns, significantly boosting the model’s robustness and generalization ability. The C3k2 module is then combined with a modified dynamic convolution module, which avoids unnecessary computational overhead while enhancing the flexibility and feature representation. Additionally, a content-guided attention fusion (HGAF) module is introduced before the detection phase, ensuring that the model assigns the correct importance to various feature maps, thereby highlighting the most relevant object details. Experimental results indicate that YOLO-EDH surpasses YOLOv11, improving the precision, recall, and mAP50 by 0.9%, 1.7%, and 1.6%, respectively. In conclusion, YOLO-EDH offers an efficient solution for ore detection in practical applications, with considerable potential for industries like intelligent mine resource sorting and safety production monitoring, showing notable commercial value. Full article
Show Figures

Figure 1

20 pages, 11264 KB  
Article
Clay Mineral Characteristics and Smectite-to-Illite Transformation in the Chang-7 Shale, Ordos Basin: Processes and Controlling Factors
by Kun Ling, Ziyi Wang, Yaqi Cao, Yifei Liu and Lin Dong
Minerals 2025, 15(9), 951; https://doi.org/10.3390/min15090951 - 5 Sep 2025
Viewed by 425
Abstract
As critical components in continental shale systems, the composition and evolution of clay minerals are fundamental to their diagenetic processes and petrophysical properties. The Chang-7 shales in the Ordos Basin exhibit abundant clay mineral content, offering a valuable case study for clay mineral [...] Read more.
As critical components in continental shale systems, the composition and evolution of clay minerals are fundamental to their diagenetic processes and petrophysical properties. The Chang-7 shales in the Ordos Basin exhibit abundant clay mineral content, offering a valuable case study for clay mineral research under moderate diagenetic conditions. This study employed XRD analysis to determine the whole-rock mineralogy, clay mineral composition, and the evolution characteristics of illite-smectite mixed-layer minerals (I/S). Comprehensive clay mineral datasets compiled from 13 newly analyzed wells and existing literature revealed distinct lateral distribution patterns. Total Organic Carbon (TOC) analysis and vitrinite reflectance (Ro) measurements provided systematic quantification of organic matter abundance and thermal maturation parameters in the studied samples. The results reveal that the Chang-7 shale exhibits a characteristic clay mineral assemblage, with I/S (average 44.2%) predominating over illite (34.7%), followed by chlorite (15.6%) and limited kaolinite (5.4%). Frequent volcanic activities provided substantial precursor materials for smectite formation, which actively participated in subsequent illitization processes, while chlorite and kaolinite distributions were predominantly controlled by provenance inputs and sedimentary facies, respectively. Inconsistencies exist between diagenetic stages inferred from I/S mixed-layer ratios and Ro values, particularly in low-maturity samples exhibiting accelerated illitization. The observed negative correlation between TOC content and mixed-layer ratios in Well YY1 and YSC Section samples demonstrates the catalytic role of organic matter in facilitating smectite-to-illite transformation. These results systematically clarify the coupled effects of sedimentary-diagenetic processes, offering new insights into the mutual interactions between inorganic and organic phases during illitization under natural geological conditions. The findings advance the understanding of Chang-7 shale oil and gas systems and offer practical guidance for future exploration. Full article
Show Figures

Figure 1

13 pages, 4027 KB  
Article
Influence of Geological Origin on the Physicochemical Characteristics of Sepiolites
by Leticia Lescano, Silvina A. Marfil, Luciana A. Castillo and Silvia E. Barbosa
Minerals 2025, 15(9), 950; https://doi.org/10.3390/min15090950 - 5 Sep 2025
Viewed by 297
Abstract
In this study the influence of the geological formation environment on the physicochemical properties of two natural sepiolites, as collected, was investigated. The samples analyzed were a lacustrine-derived sample from Tolsa, Spain (ST), and a hydrothermal-derived sample from La Adela, Argentine (SA). Comprehensive [...] Read more.
In this study the influence of the geological formation environment on the physicochemical properties of two natural sepiolites, as collected, was investigated. The samples analyzed were a lacustrine-derived sample from Tolsa, Spain (ST), and a hydrothermal-derived sample from La Adela, Argentine (SA). Comprehensive characterization was carried out using chemical analysis (XRF), X-ray diffraction (XRD), thermogravimetric analysis (TGA), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and evaluations of hydrophobicity/hydrophilicity behavior. The results indicate that the ST sample exhibits a higher SiO2/MgO ratio and contains amorphous silica impurities, while the SA sample shows a composition more closely aligned with the theoretical stoichiometry of sepiolite. Furthermore, the SA sample demonstrates greater crystallinity compared to the ST sample. Morphological analysis revealed that ST consists of compact, aggregated fibrous structures, while SA is composed of disaggregated, needle-like fibers with high aspect ratios and nanometric diameters. Both samples display predominantly hydrophilic behavior; however, only the SA sample exhibits suspended particles at the interface, suggesting a slightly higher hydrophobic character than ST sample. These findings highlight the significant impact of the geological formation environment on the structural and surface characteristics of sepiolite, which, in turn, influence its performance in applications involving dispersion, adsorption, and interfacial interactions. Full article
Show Figures

Graphical abstract

27 pages, 13959 KB  
Article
Petrogenesis of Tholeiitic Basalts from CZK06 Drill Core on the Tianchi Volcano, China–North Korea Border
by Cheng Qian, Jintao Ge, Bo Pan, Zhen Tang, Bin Jiang, Tianri Cui and Lu Lu
Minerals 2025, 15(9), 949; https://doi.org/10.3390/min15090949 - 5 Sep 2025
Viewed by 295
Abstract
To constrain Tianchi Volcano basalt petrogenesis, this study focuses on tholeiitic basalts from the CZK06 drill core on the northern slope. Using elemental geochemistry and Mg isotope analyses, we investigate magma evolution, petrogenesis, and mantle source properties. The tholeiitic basalts formed during the [...] Read more.
To constrain Tianchi Volcano basalt petrogenesis, this study focuses on tholeiitic basalts from the CZK06 drill core on the northern slope. Using elemental geochemistry and Mg isotope analyses, we investigate magma evolution, petrogenesis, and mantle source properties. The tholeiitic basalts formed during the Pliocene-Early Pleistocene shield-forming stage, recording three stages of basaltic volcanism (Phases I to III). Classified as sodium-series basalts, they exhibit geochemical affinities with EM1-type OIB. Their δ26Mg values (−0.420‰ to −0.150‰) show a substantially wider range than N-MORB. Their geochemical compositions are primarily controlled by source region characteristics and partial melting degree, with minor additional influences from fractional crystallization and crustal contamination. Fractional crystallization intensity shows a progressive increase from Phase I to III. Integrated with geochemical tracing studies of Changbaishan basalts, we propose that the tholeiitic basalts are derived predominantly from the partial melting of carbonatized pyroxenite, which originated from subducted ancient clay-rich altered oceanic crust. The carbonate melts driving the carbonatization were generated by low-pressure melting of recent oceanic sediments, transported by the deeply subducted carbonate-rich Pacific Plate within the Mantle Transition Zone. The tholeiitic magma formed in the Low-Velocity Zone at depths of 160–180 km beneath the lithospheric mantle. Full article
(This article belongs to the Special Issue Selected Papers from the 7th National Youth Geological Congress)
Show Figures

Figure 1

15 pages, 3813 KB  
Review
Resource Recycling and Ceramsite Utilization of Coal-Based Solid Waste: A Review
by Han Wang, Chunfu Liu, Chenyu Zhu and Zhipeng Gong
Minerals 2025, 15(9), 948; https://doi.org/10.3390/min15090948 - 5 Sep 2025
Viewed by 351
Abstract
Coal-based solid waste refers to solid waste generated during coal mining and washing processes, and is one of the major types of industrial solid waste in China. Its resource utilization is a critical part of the clean and efficient use of coal, and [...] Read more.
Coal-based solid waste refers to solid waste generated during coal mining and washing processes, and is one of the major types of industrial solid waste in China. Its resource utilization is a critical part of the clean and efficient use of coal, and preparing ceramsite from coal-based solid waste is an important means to promote its “resourceful, large-scale, and high-value” utilization. This paper systematically summarizes the types and properties of coal-based solid waste, its resource utilization methods, and research progress in ceramsite preparation. The focus is on assessing the feasibility, process features, and application status of ceramsite made from coal-based solid waste in areas such as construction, heavy metal stabilization, and water treatment. Using coal-based solid waste to produce ceramsite offers cost reduction and pollution mitigation benefits while showcasing significant potential for resource recycling and sustainable development. This paper further outlines the development trends and technological innovation directions for coal-based solid waste ceramsite, providing theoretical support and practical guidance for advancing the resource utilization of industrial solid waste. Full article
(This article belongs to the Special Issue Recycling and Utilization of Metallurgical and Chemical Solid Waste)
Show Figures

Figure 1

19 pages, 3396 KB  
Article
Effect of Scale Inhibitors on the Nucleation and Crystallization of Calcium Carbonate
by Vanessa Pimentel Lages, Raquel Gonçalves, Fernanda Medeiros, Rubens Bisatto, André Linhares Rossi and Amaro Gomes Barreto Junior
Minerals 2025, 15(9), 947; https://doi.org/10.3390/min15090947 - 5 Sep 2025
Viewed by 255
Abstract
Effective control of calcium carbonate (CaCO3) scale formation is crucial to improve the performance and economic efficiency of water systems. This study investigates the impact of various scale inhibitors on the nucleation and crystallization processes of CaCO3. Calcium carbonate [...] Read more.
Effective control of calcium carbonate (CaCO3) scale formation is crucial to improve the performance and economic efficiency of water systems. This study investigates the impact of various scale inhibitors on the nucleation and crystallization processes of CaCO3. Calcium carbonate particles were synthesized by mixing CaCl2·2H2O and NaHCO3 solutions, in the presence of various scale inhibitors that had not previously been investigated using the experimental techniques employed in this study. Particle size distribution and zeta potential were analyzed using dynamic light scattering (DLS), while Ca+2 consumption and pH changes were monitored with ion-selective electrodes. Crystal morphology was evaluated using scanning electron microscopy (SEM) and cryo-transmission electron microscopy (cryo-TEM). We demonstrated that, in all samples, approximately 98% of the CaCO3 particles (sized between 400 and 840 nm) are formed within the first 30 min of synthesis, and these particles then aggregate to form larger particles (840–1100 nm in size). Due to the solution’s high supersaturation, the inhibitors influence calcium consumption only after 5 min of synthesis. All inhibitors, especially DTPMP, decrease calcium consumption and particle size during synthesis. The zeta potential and morphology of the particles in the samples containing inhibitors differed from those in the control group. Cryo-TEM observations revealed distinct nanometric precursor phases in the calcite crystallization process without inhibitors and different nanostructures when scale inhibitors were used. Moreover, conchoidal fractures were observed in the nanoparticles formed in the presence of DTPMP. This study demonstrates the effectiveness of various inhibitors in reducing calcium consumption in solution and altering the morphology of CaCO3 crystals, thereby preventing calcium carbonate (CaCO3) scale formation. Full article
Show Figures

Graphical abstract

14 pages, 1849 KB  
Article
Isolation, Testing, and Adaptation of Bacteria to Bioleach Metals from Pyrite
by Anna Choińska-Pulit, Justyna Sobolczyk-Bednarek and Marcin Kania
Minerals 2025, 15(9), 946; https://doi.org/10.3390/min15090946 - 4 Sep 2025
Viewed by 339
Abstract
Bioleaching, mediated by selected microflora, offers a more environmentally friendly and cost-effective alternative to traditional mining techniques by transforming metals from sulfide ores into water-soluble forms. Pyrite ores often contain valuable rare or noble metals, such as gold (Au), silver (Ag), nickel (Ni), [...] Read more.
Bioleaching, mediated by selected microflora, offers a more environmentally friendly and cost-effective alternative to traditional mining techniques by transforming metals from sulfide ores into water-soluble forms. Pyrite ores often contain valuable rare or noble metals, such as gold (Au), silver (Ag), nickel (Ni), and cobalt (Co), which can be leached through the metabolic activity of specific chemoautotrophic microorganisms. This study investigates the adaptation process of the Acidithiobacillus ferriphilus bacterial strain, originally isolated from acid mine drainage (AMD), for the bioleaching of pyrite. The progress of the bioleaching process was evidenced by the release of iron (3.6 mg/mL) and significant quantities of gold (0.21 mg/L, equivalent to 3 g/t) into the post-culture liquid. The results indicate that the most effective bioleaching was achieved during the final adaptation stage, utilizing a medium with 7% pyrite content and a 0.75% supplement of an easily accessible energy source in the form of iron sulfate. These findings confirm the potential of the A. ferriphilus strain for pyrite bioleaching. Full article
(This article belongs to the Special Issue Advances in the Theory and Technology of Biohydrometallurgy)
Show Figures

Figure 1

Previous Issue
Back to TopTop