Search Results (115)

Multispectral satellite imagery is a very useful technique to identify altered wall rocks around orogenic gold systems. In this study in the Akzhal–Vasilyevskoye district, Kazakhstan, we show that a geology-based ASTER band-ratio workflow is a useful technique to trace metasomatic footprints of mineralization. In the West Kalba camp, beresite and listvenite both produce usable ASTER SWIR signals, while pyrite and arsenopyrite are largely featureless at multispectral resolution. Five ratios on AST_07XT surface-reflectance data, screened with upper-tail anomaly masks, have enabled identification of sericitic cores, chloritic and carbonate halos, ferric caps, and zones containing mixtures of ferrous phyllosilicates. We show that district-scale Al–OH sericitic anomalies occur within Mg–OH and carbonate shells. At Vasilyevskoye the pattern is due to beresite nuclei within listvenite rims, while at Tokum the sericitic centres remain compact within wider Mg–OH and carbonate halos. Mean polygon spectra differ between the two footprints across Bands B4–B6 and across the SWIR tail (B7–B9). SEM–EDS at Vasilyevskoye links the mapped anomalies to chlorite, sericite, and carbonate gangue assemblages with sulfide-bearing volumes. The data also allow identification of subordinate REE, phosphate, and Ti enrichment within carbonaceous and polymineralic host lithologies. Full article

Phosphate tailings (PTs), a solid waste generated from phosphate flotation, are a low-grade phosphate resource rich in quartz and dolomite. Their long-term accumulation leads to both resource loss and environmental risks, making valorization increasingly important for the sustainable development of the phosphorus chemical industry. In this study, calcareous–magnesian PTs were used as raw materials, and selective hydrothermal leaching with weakly acidic AlCl₃ solution was employed to separate the dolomite phase and directly construct a Ca-Mg-Al precursor solution for layered double hydroxides (LDHs). The LDHs were subsequently synthesized by co-precipitation and evaluated for phosphate removal from wastewater. The results showed that the precipitation pH markedly affected the phase composition and platelet morphology of the LDHs, while appropriate aging conditions further improved their adsorption performance. Under the optimal conditions of pH 12, aging at 40 °C for 2 h, the obtained LDHs exhibited the best phosphate uptake. Adsorption kinetics followed the pseudo-second-order model, and the maximum adsorption capacity calculated from the Langmuir model reached 38.61 mg-P/g. Characterization by XRD, FTIR, TG-DTA, point of zero charge, and XPS indicated that phosphate removal was dominated by surface complexation, accompanied by anion exchange, ionic precipitation, and electrostatic attraction. Full article

Magnesium ammonium phosphate cement (MAPC) exhibits rapid setting, high early strength, and potential resistance to elevated temperatures, making it a promising material for rapid repair and fire-resistant applications. Gold tailings (GT), which contain thermally stable Si- and Al-rich components, show potential for improving the high-temperature performance of MAPC. However, the mechanisms by which GT affects the residual performance and phase evolution of MAPC after exposure to elevated temperatures remain insufficiently understood. In this study, GT was used to replace the total binder in MAPC mortar at mass replacement levels of 0%, 10%, 20%, and 30%, while the MgO/NH₄H₂PO₄ mass ratio in the remaining binder was kept constant. The effects of GT content on the workability of MAPC mortar, as well as its visual appearance, mechanical properties, mass loss rate, phase evolution, and microstructure after exposure to elevated temperatures, were investigated. The results showed that GT incorporation shortened the setting time and reduced the fluidity and room-temperature strength. After exposure to elevated temperatures, the GT-containing specimens exhibited higher strength retention and lower mass loss rates. After exposure to 1000 °C, the compressive strength of the specimen containing 30% GT reached 15.37 MPa, which was approximately 44.0% higher than that of the specimen without GT. Its flexural strength retention and mass loss rate were 47.42% and 9.84%, respectively. XRD and SEM results indicated that the formation of high-temperature residual phases, including Mg₃(PO₄)₂, Mg₂SiO₄, and aluminosilicates, may contribute to the improvement of the residual matrix structure after exposure to elevated temperatures. Overall, GT incorporation improved the residual mechanical properties of MAPC after exposure to elevated temperatures, and the specimen containing 30% GT showed comparatively superior performance within the experimental scope of this study. These findings provide a reference for the resource utilization of GT in MAPC-based heat-resistant repair materials. Full article

Tailings remediation alleviates ecosystem degradation and protects species. To conserve terrestrial biodiversity and address sustainability challenges while achieving economic growth, numerous researchers have devoted efforts to monitoring ecological functions and optimizing community structures. This study investigates the microbial characteristics and functional diversity across ecological succession stages of tailings. Selecting three typical restoration stages, including biological crust, moss, and grassland stages, we adopt 16S rRNA and ITS gene amplification, Illumina high-throughput sequencing, spectroscopy, and network correlation analysis to explore the responses of soil multifunctionality index, microbial communities, and carbon metabolism during tailings restoration. The experimental results indicate that the functional diversity index increases with ecological succession and is significantly correlated with the bacterial genera Rubrobacter and Arenimicrobium, whereas no significant correlation is observed with dominant fungi. The network interactions among bacterial communities are gradually strengthened along the succession process. In terms of carbon metabolic functions, the relative abundances of galactose, starch, and sucrose metabolism pathways increase obviously with restoration progression, while inositol phosphate metabolism, peroxisome metabolism, retinol metabolism, glyoxylate and dicarboxylate metabolism, and xenobiotics metabolism exhibit no significant variations. These findings provide novel empirical evidence for explaining microbe-mediated ecological succession in tailing ecosystems and highlight the necessity of multi-perspective analysis for ecological restoration. Policy and practical implications emphasize that the application of specific microorganisms and their interspecific interactions to promote iron tailings ecological restoration should fully consider the spatiotemporal heterogeneity of tailings areas. This study deepens the understanding of differential microbial responses at different tailings restoration stages and provides actionable insights for balancing mining economic development and terrestrial ecosystem conservation. Full article

Flotation tailings and metallurgical slags from mining often contain toxic Pb, Cd, and Zn. In this study, we evaluated the in situ immobilization of Pb, Cd, and Zn in a Pb–Zn flotation tailing and a smelting slag by adding representative amendments: phosphate-based (ammonium phosphate, phosphoric acid, glassy fertiliser), cementitious (Portland cement), and iron-based (bog iron ore) materials at 1–10% (w/w). Treated samples underwent EPA-TCLP and pH-dependent leaching tests (pH 3–10), with Pb, Cd, and Zn measured by atomic absorption spectroscopy. The untreated tailing leached hazardous Pb (~60 mg/L) and elevated levels of Cd (~0.7 mg/L) and Zn (~53 mg/L), whereas the untreated slag leached negligible metal concentrations. All amendments reduced metal release in a dose-dependent manner. Phosphate amendments were most effective (e.g., 10% H₃PO₄ cut tailing Pb by 80%, Cd by 60%, and Zn by 30%), while cement and iron additions had much weaker effects. Solid-phase XRD and SEM-EDS analyses indicated the formation of stable calcium–phosphate minerals on sulfide surfaces after phosphate treatment. These findings suggest that low-cost phosphate additives (~5–10%) can substantially immobilize Pb, Cd, and Zn in such wastes. However, under strongly acidic conditions (pH < 3), some remobilization occurred, highlighting the need for further validation. This work provides practical guidance for waste managers on selecting in situ stabilization strategies for Pb–Zn mine wastes. Full article

Coal rank exerts a fundamental control on the distribution of elements during density-based separation, yet this influence remains poorly understood. The primary objective of this study is to elucidate how coal rank governs the enrichment and partitioning of major, trace, and rare earth elements (REY) in float–sink products, and to assess the implications for clean coal utilization and critical metal recovery. To achieve this, three Late Paleozoic bituminous coals of different ranks from Shanxi Province, China, were subjected to density fractionation (1.3–1.8 g/cm³) combined with proximate and ultimate analyses, X-ray fluorescence (XRF), inductively coupled plasma mass spectrometry (ICP-MS), X-ray diffraction (XRD), and coal petrography. The results show that coal rank fundamentally governs element distribution and enrichment patterns. With increasing rank, the dominant inorganic minerals shift from clay minerals to carbonates, leading to pronounced differentiation in elemental affinities. In medium- to high-rank bituminous coals, chalcophile elements (e.g., As, Mo, Tl) associated with sulfides are significantly enriched in high-density fractions, whereas in high-rank bituminous coals, carbonate-related elements (e.g., Sr, Ca, Mg) show marked enrichment. Rare earth elements are primarily hosted in clay and phosphate minerals. Light rare earth elements dominate in medium- to high-rank coals, while middle rare earth elements increase in high-rank coals due to carbonate influence. Density-based separation effectively concentrates hazardous elements (e.g., As, Pb, Cd) in high-density tailings, demonstrating substantial potential for mitigating environmental risks. Meanwhile, critical metals such as lithium (Li), strontium (Sr), and REY are enriched in medium- to high-density products, with Li hosted in clay minerals and Sr strongly enriched in carbonate-rich high-rank coal (up to 1525 μg/g), indicating recoverable resources from coal processing wastes. Full article

Phosphogypsum (PG) is an industrial solid waste whose use in cementitious materials is limited by strength reduction at high dosages. This study evaluated a clinker-free multi-solid-waste binder containing 40 wt.% PG for cemented paste backfill using steel slag powder (SSP) and granulated blast-furnace slag (GBFS) as co-binders, with phosphate mine tailings and slime as aggregates. Uniaxial compressive strength (UCS), X-ray diffraction, scanning electron microscopy, and nuclear magnetic resonance were combined with image-based pore-structure sensitivity analysis to examine the relationships among hydration products, pore evolution, and strength development. The results showed that AFt and C–S–H-like gels were associated with pore refinement and strength gain. All mixtures reached UCS values above 0.5 MPa at 7 days and 1.0 MPa at 28 days. The A2 mixture achieved the highest 7-day UCS of 0.8 MPa, whereas A1 showed the highest 28-day UCS of 1.6 MPa. Porosity, pore probability entropy, and fractal dimension were negatively correlated with UCS, with pore probability entropy showing the highest sensitivity to 7-day strength. These findings support the use of high-PG clinker-free binders for targeted phosphate-mine backfill. Full article

This study investigates the environmental and health impacts of potentially toxic elements (PTEs) in solid and liquid wastes from phosphate beneficiation and fertilizer production in the Mdhilla area, Gafsa Basin, Tunisia. Solid wastes, including phosphate tailings (PTs) and phosphogypsum (PG), and associated industrial effluents from phosphate beneficiation (PBE) and fertilizer production (PFE), were characterized using physicochemical analysis, ICP-MS, SEM–EDX, and ion chromatography. Single and integrated pollution indices, along with conservative human health risk assessments, were applied to evaluate cumulative contamination and potential risks. PT exhibited near-neutral pH (7.64) and high PTE enrichment (Zn 350 mg kg⁻¹, Cr 329 mg kg⁻¹, Cd 38.8 mg kg⁻¹), whereas PG was strongly acidic (pH 3.13) and comparatively depleted in metals, reflecting process-dependent partitioning. Despite neutral pH, PBEs contained markedly higher metal concentrations than PFEs, with Fe (163 mg L⁻¹), Cr (3.09 mg L⁻¹), Cd (0.49 mg L⁻¹), and Pb (0.71 mg L⁻¹) exceeding discharge limits. Pollution indices indicated severe to extreme contamination, with PBE showing an exceptionally high contamination degree (C_deg = 63,659) compared to PFE (C_deg = 12,815), and elevated Toxic Element Pollution Index (PTEPI) values confirmed stronger cumulative pollution in PBE. Potential ecological risk indices (PERI > 600) revealed very high ecological risk for both effluents, primarily driven by Cd, Co, and Tl. Although dermal contact may represent the most frequent exposure route, risk assessment results indicated that accidental oral ingestion is the dominant pathway contributing to both non-carcinogenic and carcinogenic risks, with children being particularly vulnerable. Non-carcinogenic risk thresholds (HQ > 1) were exceeded for PBE, while total carcinogenic risks approached or exceeded regulatory limits (10⁻⁶–10⁻⁴), mainly due to Cd and Cr. Overall, phosphate beneficiation was the primary source of cumulative metal loading and associated ecological and health risks, while fertilizer production partially reduced contamination. These findings underscore the urgent need for improved management and mitigation of phosphate-processing wastes in industrial regions. Full article

In this study, the characteristics of sulfide minerals during the acidic double reverse flotation of phosphate ore and the adsorption mechanisms of sodium oleate (NaOL) and dodecyl trimethyl ammonium bromide (DTAB) were investigated. Micro-flotation test results indicated that NaOL effectively collected galena, sphalerite, and pyrite at a concentration of 1 × 10⁻³ mol/L and pH 4–5.5, whereas DTAB exhibited selectivity for galena at 1 × 10⁻⁴ mol/L. Mixed mineral flotation revealed that NaOL induced a non-selective bulk flotation of sulfides with dolomite, resulting in a high froth yield of 93.23%, while the DTAB system showed superior selectivity with a froth yield of 54.91%. Surface analyses (Zeta potential, FTIR, and XPS) confirmed that NaOL chemisorbs onto sulfide surfaces via metal-oleate complexes, whereas DTAB adsorption is dominated by electrostatic attraction. Bench-scale tests validated the “double-rejection” flowsheet, significantly upgrading the P₂O₅ grade from 23.38% to 31.47% by sequentially partitioning Pb, Zn and Fe into the froth tailings. Size-by-assay analysis indicated that the sulfide separation was primarily controlled by the extent of mineral liberation. These findings provide a robust theoretical framework and practical guidance for the simultaneous management of sulfide minerals during phosphate beneficiation. Full article

Fluorapatite is a typical phosphate rock resource. Fluorapatite tends to generate fine mud agglomeration, which induces dehydration challenges owing to its inherently fine particle size and negative surface charge. In this paper, phosphate tailings slurries from a phosphate mine in Hubei Province, China, were selected as the research object, and flocculation–dehydration experiments were conducted using anionic, cationic, and nonionic polyacrylamide (PAM) flocculants. The results show that the maximum settling velocity is 51 mm/s and the moisture content of filter cake is 41.54%, which were obtained when the unit consumption of cationic flocculant with molecular weight 12 million was 1000 g/t. The mechanism of sedimentation and dehydration was studied by infrared spectroscopy and a particle size analyzer. The results showed that polyacrylamide was effectively adsorbed on the mineral surface, and the size of flocs increased significantly. Finally, the mechanism of sedimentation and dehydration was proposed. It has important guiding significance for the efficient solid–liquid separation and water circulation of fluorapatite mineral processing wastewater. Full article

To promote the resource recovery of phosphate mine tailings and alleviate the pressure caused by the growing scarcity of river sand, this study employs a research methodology combining macroscopic performance analysis with microscopic testing to systematically investigate the effects of three types of recycled sand containing varying proportions of phosphate mine tailings (flint (FS), phosphorite flint (PFS) and dolomitic limestone (DLS)) on the performance of mortar. The study focused on assessing the impact of recycled sand on the workability of mortar, water absorption, mechanical properties, pore structure, cement hydration characteristics, and environmental safety, and conducted a comprehensive evaluation of the project’s feasibility in conjunction with a cost analysis. The effect of DLS was most pronounced in terms of setting time. Water absorption tests show that when the proportions of FS, PFS, and DLS are all 25%, the mortar’s water absorption reaches its minimum value. In terms of mechanical properties, DLS showed a more pronounced increase in early-stage flexural strength, whilst PFS and FS demonstrated a more significant increase in later-stage strength. In terms of compressive strength improvement, PFS outperformed both FS and DLS. XRD and TG-DTA test results show that the three kinds of recycled sand have no adverse effect on cement hydration. SEM and MIP results confirmed that compared with river sand, the porosity of mortar mixed with FS was smaller and the pore structure was denser. Environmental safety assessments have shown that the heavy metal leaching concentrations in the mortar made from the three types of recycled sand are all significantly below the national limits, indicating good environmental compatibility. An economic analysis indicates that the “25% river sand + 75% FS” alternative offers the best economic benefits, resulting in cost savings of 93.27 CNY per cubic metre. In summary, the use of recycled sand derived from phosphate ore tailings as a substitute for river sand in the preparation of mortar is feasible from technical, environmental, and economic perspectives. This approach facilitates the recovery of solid waste resources, conserves natural resources, reduces the environmental burden, and promotes cost optimisation. Full article

Phosphogypsum (PG), a major by-product of the phosphate industry, has potential for improving acidic and nutrient-poor red soils, yet its agronomic benefits and heavy metal risks require systematic evaluation. A field experiment was conducted with five treatments, CK (soil only), GT (50% modified phosphogypsum, MPG), TT (40% MPG), ZT (50% phosphorite tailings), and DT (25% MPG + 25% lake sediment), to assess their effects on soil properties, enzyme activities, peanut growth, yield, quality, and heavy metal accumulation. All amendments improved soil structure, moisture retention, nutrient availability, and enzymatic activities. Peanut pod and kernel yields increased under all treatments, with DT achieving the greatest improvements (29.89% and 40.88%, respectively), whereas ZT showed the weakest response (1.91% and 6.26%). DT also achieved the highest soil quality index, and performed best in both yield improvement and root development. Although Cd accumulation increased under DT, heavy metal concentrations in peanut kernels remained below national food safety limits. Overall, DT was identified as the most effective amendment for enhancing red soil fertility and peanut productivity, while long-term monitoring of Cd bioavailability is recommended to ensure sustainable and safe application. Full article

Two mineral-based solid residues, namely coal gangue (CG) and phosphorus tailings (PT), two of the largest solid waste streams in the mining industry, were used as the sole metal feedstocks to fabricate a novel MgCaFeAl layered double hydroxide (LDH-GT) via a 700 °C calcination, acid leaching and hydrothermal coprecipitation route, with simultaneous synthesis of white carbon black from the reaction byproducts. Under optimized conditions (total metal load is 150 mg kg⁻¹, LDH-GT dose is 0.09 g, pH from 6 to 7), the synthesized material achieved concurrent immobilization efficiencies of 76.28%, 99.96%, and 99.95% for Cr (VI), Cd (II) and Ni (II), respectively, within a 24 h reaction period. TCLP leachability decreased by 82 to 91% relative to the untreated soil. After three wetting, drying and freeze–thaw cycles, the leached concentrations of all three metals remained below 0.3 mg L⁻¹, confirming excellent long-term stability. Mechanistic analyses revealed that Cr (VI) was mainly sequestered through interlayer anion exchange and surface complexation, whereas Cd (II) and Ni (II) were immobilized via isomorphic substitution into the LDH lattice, precipitation as carbonates, and incorporation into Fe/Mn oxides. A 7-day mung bean bioassay showed that LDH-GT amendment increased seed germination from 50% to 73%, enhanced root and shoot biomass by 1.1- to 1.6-fold, and decreased plant Cr, Cd, and Ni contents by over 80%. The 16S rRNA sequencing further demonstrated that LDH-GT reversed the decline in microbial α diversity induced by heavy metal stress, restored aerobic chemoheterotrophic and sulfur cycling functional guilds, and reduced pathogenic signatures. This study provides the demonstration of a waste-to-resource LDH that achieves efficient, durable remediation of multi-metal-contaminated soils, offering a scalable route for coupling solid waste valorization with in situ site restoration. Full article

Mediator is a central transcriptional coactivator that connects sequence-specific transcription factors with RNA polymerase II to control inducible gene expression in plants. MED16 is a Mediator tail module subunit that functions as a context-dependent integrator, helping coordinate developmental programs with environmental adaptation. This review summarizes current evidence for MED16 function from structural and evolutionary perspectives to physiological outputs, with emphasis on how MED16 interacts with transcription factors and other Mediator subunits to shape RNA polymerase II engagement at target loci. In terms of development, MED16 contributes to organ growth and root system architecture, and comparative studies have revealed that it plays conserved roles in lineage-specific wiring. Under abiotic stress, MED16 supports the efficient activation of stress-inducible transcription, including cold acclimation and nutrient stress responses such as phosphate starvation-dependent root remodeling. In immunity, MED16 modulates salicylic acid- and jasmonate/ethylene-associated defence outputs and can be targeted by plant viruses, which is consistent with its role in antiviral transcriptional responses. Mechanistically, MED16 participates in cooperative and competitive interactions within the Mediator complex that tune hormone-responsive outputs, exemplified by MED25-related competition in abscisic acid signalling. We highlight key limitations and future directions, including the need for mechanistic validation beyond Arabidopsis, clearer models of dosage control in crops, improved understanding of context-dependent tail configurations, and high-resolution mapping of MED16 interaction interfaces. Full article

The global environmental challenges of solid waste accumulation and aquatic eutrophication demand innovative and sustainable strategies. This study introduces a circular “waste-treats-waste” approach by converting dolomite-rich phosphate tailings (PT), a widespread industrial by-product, into a high-value adsorbent for phosphorus (P) removal. Thermal modification at 950 °C for 1 h dramatically enhanced the adsorption capacity by approximately 45 times, from 2.52 mg/g (raw PT) to 112.41 mg/g. This performance is highly competitive with, and often superior to, many engineered adsorbents. The calcination process was pivotal, decomposing carbonates into highly active CaO and MgO while developing a porous structure. Using a multi-technique characterization approach (X-ray diffraction (XRD), Fourier transform infrared spectra (FTIR), TESCAN VEGA3 tungsten filament scanning electron microscope (SEM), the Brunauer–Emmett–Teller method (BET)), the key immobilization mechanism was identified as hydroxyapatite formation, driven by Ca²⁺/Mg²⁺-phosphate precipitation and surface complexation. Nonlinear regression analysis revealed that the adsorption kinetics obeyed the pseudo-second-order model, and the equilibrium data were best described by the Freundlich isotherm. This indicates a chemisorption process occurring on a heterogeneous surface, consistent with the complex structure created by thermal modification. Notably, post-adsorption pore structure expansion suggested synergistic pore-filling and surface reorganization. This work not only demonstrates a circular economy paradigm for repurposing industrial solid waste on a global scale but also offers a cost-effective and high-performance pathway for controlling phosphorus pollution in aquatic systems, contributing directly to resource efficiency and sustainable environmental remediation. Full article