Search Results (815)

This study aims to evaluate eco-innovative solutions in the fertilizer industry that allow for waste valorization in the context of a resource-efficient circular economy. A comprehensive reuse strategy was developed for low-rank peat and post-cultivation horticultural mineral wool, involving the extraction of valuable humic substances from peat and residual nutrients from used mineral wool, followed by the use of both post-extraction residues to produce organic–mineral substrates. The resulting products/semifinished products were characterized in terms of their composition and properties, which met the requirements necessary to obtain the admission of this type of product to the market in accordance with the Regulation of the Minister for Agriculture and Rural Development of 18 June 2008 on the implementation of certain provisions of the Act on fertilizers and fertilization (Journal of Laws No 119, item 765). Elemental analysis, FTIR spectroscopy, and solid-state CP-MAS ¹³C NMR spectroscopy suggest that post-extraction peat has a relatively condensed structure with a high C content (47.4%) and a reduced O/C atomic ratio and is rich in alkyl-like matter (63.2%) but devoid of some functional groups in favor of extracted fulvic acids. Therefore, it remains a valuable organic biowaste, which, in combination with post-extraction waste mineral wool in a ratio of 60:40 and possibly the addition of mineral nutrients, allows us to obtain a completely new substrate with a bulk density of 264 g/m³, a salinity of 7.8 g/dm³ and a pH of 5.3, with an appropriate content of heavy metals and with no impurities, meeting the requirements of this type of product. A liquid fertilizer based on an extract containing previously recovered nutrients also meets the criteria in terms of quality and content of impurities and can potentially be used as a fertilizing product suitable for agricultural crops. This study demonstrates a feasible pathway for transforming specific waste streams into valuable agricultural inputs, contributing to environmental protection and sustainable production. The production of a new liquid fertilizer using nutrients recovered from post-cultivation mineral wool and the preparation of an organic–mineral substrate using post-extraction solid residue is a rational strategy for recycling hard-to-biodegrade end-of-life products. Full article

In the present work, six biochars were produced from the pyrolysis of poultry manure at 400 °C and 600 °C (PM-B-400 and PM-B-600), and their post-modification with, respectively, iron chloride (PM-B-400-Fe and PM-B-600-Fe) and potassium permanganate (PM-B-400-Mn and PM-B-600-Mn). First, these biochars were deeply characterized through the assessment of their particle size distribution, pH, electrical conductivity, pH at point-zero charge, mineral composition, morphological structure, and surface functionality and crystallinity, and then valorized as biofertilizer to grow spring barley at pot-scale for 40 days. Characterization results showed that Fe- and Mn-based nanoparticles were successfully loaded onto the surface of the post-modified biochars, which significantly enhanced their structural and surface chemical properties. Moreover, compared to the control treatment, both raw and post-modified biochars significantly improved the growth parameters of spring barley plants (shoot and root length, biomass weight, and nutrient content). The highest biomass production was obtained for the treatment with PM-B-400-Fe, owing to its enhanced physico-chemical properties and its higher ability in releasing nutrients and immobilizing heavy metals. These results highlight the potential use of Fe-modified poultry manure-derived biochar produced at low temperatures as a sustainable biofertilizer for soil enhancement and crop yield improvement, while addressing manure management issues. Full article

Environmental sustainability and responsible resource utilization are critical global challenges. In this work, we present a sustainable and circular-economy-based approach for synthesizing CuFe₂O₄ nanoparticles by directly utilizing copper oxide minerals sourced from Chilean mining operations. Copper sulfate (CuSO₄) was extracted from these minerals through acid leaching and used as a precursor for nanoparticle synthesis via both chemical co-precipitation and microwave-assisted methods. The influence of different precipitating agents—NaOH, Na₂CO₃, and NaF—was systematically evaluated. XRD and FESEM analyses revealed that NaOH produced the most phase-pure and well-dispersed nanoparticles, while NaF resulted in secondary phase formation. The microwave-assisted method further improved particle uniformity and reduced agglomeration due to rapid and homogeneous heating. Electrochemical characterization was conducted to assess the suitability of the synthesized CuFe₂O₄ for supercapacitor applications. Cyclic voltammetry (CV) and galvanostatic charge–discharge (GCD) measurements confirmed pseudocapacitive behavior, with a specific capacitance of up to 1000 F/g at 2 A/g. These findings highlight the potential of CuFe₂O₄ as a low-cost, high-performance electrode material for energy storage. This study underscores the feasibility of converting primary mined minerals into functional nanomaterials while promoting sustainable mineral valorization. The approach can be extended to other critical metals and mineral residues, including tailings, supporting the broader goals of a circular economy and environmental remediation. Full article

Heavy metal contamination in natural waters and soils poses a significant environmental challenge, necessitating efficient and sustainable water treatment solutions. This study presents the computational design of low-density polyethylene (LDPE) films functionalized with iron oxide (Fe₃O₄) nanoparticles (NPs) for enhanced water purification applications. Composite materials containing 5%, 10%, and 15% were synthesized and characterized in terms of adsorption efficiency, surface morphology, and reusability. Advanced molecular modeling using BIOVIA Pipeline was employed to investigate charge distribution, functional group behaviour, and atomic-scale interactions between polymer chains and metal ions. The computational results revealed structure–property relationships crucial for optimizing adsorption performance and understanding geochemically driven interaction mechanisms. The LDPE/Fe₃O₄ composites demonstrated significant removal efficiency of Cu²⁺ and Ni²⁺ ions, along with favourable mechanical properties and regeneration potential. These findings highlight the synergistic role of mineral–polymer interfaces in water remediation, presenting a scalable approach to designing multifunctional polymeric materials for environmental applications. This study contributes to the growing field of polymer-based adsorbents, reinforcing their value in sustainable water treatment technologies and environmental protection efforts. Full article

Halogenated flame retardants have been amongst the most widely used and effective solutions for enhancing fire resistance. However, their use is currently strictly regulated due to serious health and environmental concerns. In this context, phosphorus-based and mineral flame retardants have emerged as promising alternatives. Despite this, their combined use is neither straightforward nor guaranteed to be effective. This study scrutinizes the interactions between these two classes of flame retardants (FR) through a systematic analysis aimed at elucidating the antagonistic pathways that arise from their coexistence. Specifically, this study focuses on two inorganic fillers, mineral huntite and chemically precipitated magnesium hydroxide, both of which produce basic oxides upon thermal decomposition. These fillers were incorporated into a poly(butylene terephthalate) (PBT) matrix to be utilized as advanced-mattress FR coating fabric and were subjected to a series of flammability tests. The pyrolysis products of the prepared polymeric composite compounds were isolated and thoroughly characterized using a combination of analytical techniques. Thermogravimetric analysis (TGA) and differential thermogravimetric analysis (dTGA) were employed to monitor decomposition behavior, while the char residues collected at different pyrolysis stages were examined spectroscopically, using FTIR-ATR and Raman spectroscopy, to identify their structure and the chemical reactions that led to their formation. X-ray diffraction (XRD) experiments were also conducted to complement the spectroscopic findings in the chemical composition of the resulting char residues and to pinpoint the different species that constitute them. The morphological changes of the char’s structure were monitored by scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDS). Finally, the Limited Oxygen Index (LOI) and UL94 (vertical sample mode) methods were used to assess the relative flammability of the samples, revealing a significant drop in flame retardancy when both types of flame retardants are present. This reduction is attributed to the neutralization of acidic phosphorus species by the basic oxides generated during the decomposition of the basic inorganic fillers, as confirmed by the characterization techniques employed. These findings underscore the challenge of combining organophosphorus with popular flame-retardant classes such as mineral or basic metal flame retardants, offering insight into a key difficulty in formulating next-generation halogen-free flame-retardant composite coatings. Full article

The paper proposes a putative prebiotic scenario leading to homochirality in the RNA world. In this scenario, racemic ribose, the only chiral moiety in RNA, was enantioseparated (in its pyranose form) on a chiral surface formed by the adsorption of (prochiral) nucleobases (NBs) on a mineral or metal. Purine bases (adenine and guanine) are more likely candidates for this process than pyrimidine bases because they have more H-bond donors and acceptors. Another possible candidate surface for the enantioseparation of ribose would be formed by the adsorption of nucleobase pairs, e.g., guanine–cytosine (GC). Interactions of ribose molecules with hydrogen bond donors and acceptors of NBs or NB pairs (located on the surface) enforced the orientation of ribose molecules in two directions perpendicular to each other and parallel to the surface. Consequently, the energy of interactions of enantiomers of the sugar with the surface was not the same. Thus, a solvent moving along the surface caused the enantiomers of ribose to move with different rates, resulting in the enantioseparation of ribose in a chromatography-like process. The same process would also separate ribose from other monosaccharides in the mix. Hydrogen bonding between nucleobases was also pivotal in the formation of large homochiral domains on the surfaces. Full article

Due to its persistence and potential negative effects on ecosystems and human health, microplastic pollution in aquatic environments has become a major worldwide concern. Photocatalytic degradation is a sustainable manner to degrade microplastics to non-toxic by-products. In this review, comprehensive discussion focuses on the synergistic effects of various photocatalytic materials including TiO₂, ZnO, WO₃, graphene oxide, and metal–organic frameworks for producing heterojunctions and involving multidimensional nanostructures. Such mechanisms can include the generation of reactive oxygen species and polymer chain scission, which can lead to microplastic breakdown and mineralization. The advancements of material modifications in the (nano)structure of photocatalysts, doping, and heterojunction formation methods to promote UV and visible light-driven photocatalytic activity is discussed in this paper. Reactor designs, operational parameters, and scalability for practical applications are also reviewed. Photocatalytic systems have shown a lot of development but are hampered by shortcomings which include a lack of complete mineralization and production of intermediary secondary products; variability in performance due to the fluctuation in the intensity of solar light, limited UV light, and environmental conditions such as weather and the diurnal cycle. Future research involving multifunctional, environmentally benign photocatalytic techniques—e.g., doped composites or composite-based catalysts that involve adsorption, photocatalysis, and magnetic retrieval—are proposed to focus on the mechanism of utilizing light effectively and the environmental safety, which are necessary for successful operational and industrial-scale remediation. Full article

During the operation of structures, the components and materials from which they are made are exposed to various environmental, technological, and operational impacts. In this context, the use of a modified water-dispersion composition containing finely dispersed fillers with enhanced protective and performance characteristics proves to be effective. This article examines the development of a paint-and-coating composition using hollow glass microspheres and modified diatomite as finely dispersed fillers. The influence of technological factors on the properties of coating materials based on a synthesized acrylic dispersion and fillers—such as modified diatomite and hollow glass microspheres ranging from 20 to 100 μm in size with a bulk density of 0.107–0.252 g/cm³—is analyzed. The optimal formulation of the coating materials was determined to ensure the required coating quality. Experimental results demonstrate the improved strength and hardness of the coating due to the use of acrylic dispersion obtained through an emulsifier-free method and modifiers in the form of finely dispersed fillers. It has been established that the resulting samples also exhibit high adhesion to mineral and metallic substrates, along with excellent corrosion resistance. Moreover, the incorporation of acrylic dispersion contributes to increased elasticity of the coating, resulting in improved resistance to washing and abrasion. The developed protective material can be applied to a variety of surfaces, including walls, ceilings, and roofs of buildings and structures, pipelines, and many other applications. Thus, modified water-dispersion compositions based on synthesized acrylic dispersion showed the following results: resistance to sticking—5, which is the best; chemical resistance and gloss level with standard single-phase acrylic dispersion—no destruction or change in gloss. The adhesion of coatings cured under natural conditions and under the influence of UV radiation was 1 point. The developed formulations for obtaining water-dispersion paint and varnish compositions based on synthesized polymer dispersions, activated diatomite, and hollow glass microspheres, meet all the regulatory requirements for paint and varnish materials in terms of performance, and in terms of economic indicators, the cost of 1 kg of paint is 30% lower than the standard. Full article

The Sidi Aissa Pb-Zn-(Ag) District, located within the Nappe Zone of northern Tunisia, has been reinterpreted as a typical intermediate-sulfidation (IS) epithermal mineralization system based on field observations and lithogeochemical analyses. Previously described as vein-style Pb-Zn deposits, the local geological framework is dominated by extensional normal faults forming half-grabens. These faults facilitated the exhumation of deep Triassic autochthonous rocks and the extrusion of 8-Ma rhyodacites and Messinian basalts. These structures, functioning as pathways for magmatic-hydrothermal fluids, facilitated the upward migration of acidic fluids, which interacted with the surrounding wall rocks, forming a subsurface alteration zone. The mineralization, shaped by Miocene extensional tectonics and magmatic activity, occurred in three stages: early quartz-dominated veins, an intermediate barite-rich phase, and late-stage supergene oxidation. Hydrothermal alteration, characterized by silicification, argillic, and propylitic zones, is closely associated with the deposition of base metals (Pb, Zn) and silver. The mineral assemblage, including barite, galena, sphalerite, and quartz, reflects dynamic processes such as fluid boiling, mixing, and pressure changes. Full article

Municipal solid waste (MSW) and refuse-derived fuel (RDF) incineration generate over 20 million tons of residues annually in the EU. These include bottom ash (IBA), fly ash (FA), and air pollution control residues (APCr), which pose significant environmental challenges due to their leaching potential and hazardous properties. While these residues contain valuable metals and reactive mineral phases suitable for carbonation or alkaline activation, chemical, techno-economic, and policy barriers have hindered the implementation of sustainable, full-scale management solutions. Accelerated carbonation technology (ACT) offers a promising approach to simultaneously sequester CO₂ and enhance residue stability. This review provides a comprehensive assessment of waste incineration residue carbonation, covering 227 documents ranging from laboratory studies to field applications. The analysis examines reactor designs and process layouts, with a detailed classification based on material characteristics, operating conditions, investigated parameters, and the resulting pollutant stabilization, CO₂ uptake, or product performance. In conclusion, carbonation-based approaches must be seamlessly integrated into broader waste management strategies, including metal recovery and material repurposing. Carbonation should be recognized not only as a CO₂ sequestration process, but also as a binding and stabilization strategy. The most critical barrier remains chemical: the persistent leaching of sulfates, chromium(VI), and antimony(V). We highlight what we refer to as the antimony problem, as this element can become mobilized by up to three orders of magnitude in leachate concentrations. The most pressing research gap hindering industrial deployment is the need to design stabilization approaches specifically tailored to critical anionic species, particularly Sb(V), Cr(VI), and SO₄²⁻. Full article

The mineral processing of a low-grade tungsten-molybdenum ore (LGTMO) was investigated to assess the potential of recovering molybdenum (Mo) and tungsten (W). Techniques such as Polarizing Microscope (PM), Scanning Electron Microscopy-Energy Dispersive Spectroscopy (SEM-EDS), Mineral Liberation Analysis (MLA), and Advanced Mineral Identification and Characterization System (AMICS) were employed. The recoverable metals in the ore are Mo (0.158% ± 0.03%) and W (0.076% ± 0.02%). Mo exists in two forms: 63.30% as molybdenite and 36.7% as powellite (CaMo_xW_1−xO₄). W is present as 75.26% scheelite and 24.74% powellite. The complete dissociation rates of molybdenite and scheelite-powellite are 27.14% and 88.87%, respectively. Particles of scheelite-powellite with a diameter less than 10 µm account for 34.61%, while molybdenite particles with a diameter below 10 µm make up 72.73%. Scheelite-powellite is mainly associated with olivine and dolomite, while molybdenite is mainly associated with pyroxene, calcite, and hornblende. Based on the process mineralogy, the mineralogical factors influencing the flotation recovery of molybdenite and scheelite-powellite were analyzed. Finally, a complete hydrometallurgical leaching test was carried out. The optimal experimental conditions are as follows: liquid-solid ratio of 6 mL/g, KMnO₄ concentration of 0.015 mol/L, Na₂CO₃ concentration of 0.12 mol/L, NaHCO₃ concentration of 0.024 mol/L, leaching time of 4 h, and leaching temperature of 85 °C. Under these conditions, the leaching efficiencies of Mo and W reach 79.23% and 41.41%, respectively. This study presents a novel approach for the recovery of refractory W and Mo resources in LGTMO while simultaneously providing a theoretical basis for the high-efficiency utilization of these resources. Full article

Mineralogical variability exerts a profound influence on the flotation performance of Platinum Group Metal (PGM) ores, particularly those from the Platreef deposit, where complex associations and textures influence recovery, grade, and kinetics. This study integrates the Mode of Occurrence (MOC) and mineral associations into a modified Kelsall flotation kinetics model, optimized using a Particle Swarm Optimization (PSO) algorithm, to improve prediction accuracy. Batch flotation tests were conducted on eight samples from two lithologies—Pegmatoidal Feldspathic Pyroxenite (P-FPX) and Feldspathic Pyroxenite (FPX)—with mineralogical characterization performed using MLA, QEMSCAN, and XRD. PGMs in liberated (L) and sulfide-associated (SL) forms accounted for up to 90.6% (FPX1), exhibiting high fast-floating fractions (θ_f = 0.77–0.84) and fast flotation rate constants (K_f = 1.45–1.78 min⁻¹). In contrast, PGMs locked in silicates (G class) showed suppressed kinetics (K_f < 0.09 min⁻¹, K_s anomalies up to 8.67 min⁻¹) and were associated with lower recovery (P-FPX3 = 83.25%) and increased model error (P-FPX4 = 57.3). FPX lithologies achieved the highest cumulative recovery (FPX4 = 90.35%) and the best concentrate grades (FPX3 = 116.5 g/t at 1 min), while P-FPX1 had the highest gold content (10.45%) and peak recovery (94.37%). Grade-recovery profiles showed steep declines after 7 min, particularly in slow-floating types (e.g., P-FPX2, FPX2), with fast-floating lithologies stabilizing above 85% recovery at 20 min. The model yielded R² values above 0.97 across all samples. This validates the predictive power of MOC-integrated flotation kinetics for complex PGM ores and supports its application in geometallurgical plant design. Model limitations in capturing complex locked ore textures (SAG, G classes) highlight the need for reclassification based on floatability indices and further integration of machine learning methods. Full article

This study investigates the weathering crust composite of serpentine, pyroxenite and granite in the Niangniangmiao area, the weathering crusts inside and outside the mining area were compared respectively, systematically revealing the distribution patterns, migration pathways, and ecological element activity characteristics of high-background elements (e.g., chromium (Cr) and nickel (Ni)) through precise sampling, the Tessier five-step sequential extraction method, and a migration coefficient model. Key findings include: (1) Element distribution and controlling mechanisms: The average Cr and Ni contents in the serpentinite profile are significantly higher than those in pyroxenite. However, the semi-weathered pyroxenite layer exhibits an inverted Cr enrichment ratio in relation to serpentinite, 1.8× and 1.2×, respectively, indicating that mineral metasomatic sequences driven by hydrothermal alteration dominate element differentiation; the phenomenon of inverted enrichment of high-background elements occurs in the weathering crust profiles of the two basic rocks. (2) Dual impacts of mining activities on heavy metal enrichment: Direct mining increases topsoil Cr content in serpentinite by 40% by disrupting parent material homology, while indirect activities introduce exogenous Zn and Cd (Spearman correlation coefficients with Cr/Ni are from ρ = 0.58 to ρ = 0.72). Consequently, the bioavailable fraction ratio value of Ni outside the mining area (21.14%) is significantly higher than that within the area (14.30%). (3) Element speciation and ecological element activity: Over 98% of Cr in serpentine exists in residual fractions, whereas the Fe-Mn oxide-bound fraction (F3) of Cr in extra-mining pyroxenite increases to 5.15%. The element activity in ecological systems ranking of Ni in soil active fractions (F1 + F2 = 15%) follows the order: granite > pyroxenite > serpentine. Based on these insights, a scientific foundation for targeted remediation in high-background areas (e.g., prioritizing the treatment of semi-weathered pyroxenite layers) can be provided. Full article

A varied family of polyphenolic chemicals, flavonoids, are becoming more and more important in bone tissue engineering because of their osteogenic, anti-inflammatory, and antioxidant effects. Recent developments incorporating flavonoids into different biomaterial platforms to improve bone regeneration are emphasized in this study. Osteocalcin (OCN) expression was 2.1-fold greater in scaffolds loaded with flavonoids—such as those made of polycaprolactone (PCL)—greatly increasing human mesenchymal stem cell (hMSC) proliferation and mineralization. Comparably, a threefold increase in calcium deposition indicates increased mineralization when hydroxyapatite (HA) was functionalized with flavonoids such as quercetin. These HA scaffolds with flavonoids also showed a 45% decrease in osteoclast activity, therefore promoting balanced bone remodeling. Concurrent with flavonoids like EGCG and quercetin, chitosan-based scaffolds encouraged osteogenic differentiation with increases in osteogenic markers like osteopontin (OPN) and alkaline phosphatase (ALP) expression by up to 82%. These scaffolds also showed 82% bone defect repair after six weeks in vivo, suggesting their promise in rapid bone regeneration. With an increase of up to 32% in the bone volume-to-total volume ratio (BV/TV) and 28% greater bone–implant contact (BIC), flavonoid coatings on titanium implants enhanced osteointegration in implantology. Displaying successful osteogenesis and immunomodulation, the addition of flavonoids into metal–organic frameworks (MOFs) and injectable hydrogels demonstrated a 72% increase in new bone formation in vivo. Though further research is required to confirm long-term clinical effectiveness, these findings show the great promise of flavonoid-functionalized biomaterials in bone regeneration. Full article

To ensure the green, safe, and efficient extraction of mineral resources and promote sustainability, the stability of mined-out areas has become a critical factor affecting safe production and ecological restoration in underground metal mines. The instability of underground goafs poses a significant threat to mine safety, especially when irregular excavation patterns interact with high ground stress, exacerbating instability risks. Most existing studies lack a systematic and multidisciplinary integrated framework for comprehensive evaluation and management. This paper proposes a trinity research system of “assessment–optimization–governance”, integrating theoretical analysis, three-dimensional fluid–solid coupling numerical simulation, and a filling sequence optimization method based on genetic algorithms. An analysis of data measured from 243 pillars and 49 goafs indicates that approximately 20–30% of the pillars have a factor of safety (FoS) below 1.0, signaling immediate instability risks; additionally, 58% do not meet the threshold for long-term stability (FoS ≥ 1.5). Statistical and spatial analyses highlight that pillar width-to-height ratio (W/H) and cross-sectional area significantly influence stability; when W/H exceeds 1.5, FoS typically surpasses 2.0. Numerical simulations reveal pore water pressures of 1.4–1.8 MPa in deeper goafs, substantially reducing effective stress and accelerating plastic zone expansion. Stability classification categorizes the 49 goafs into 7 “poor”, 37 “moderate”, and 5 “good” zones. A genetic algorithm-optimized filling sequence prioritizes high-risk area remediation, reducing maximum principal stress by 60.96% and pore pressure by 28.6%. Cemented waste rock filling applied in high-risk areas, complemented by general waste rock filling in moderate-risk areas, significantly enhances overall stability. This integrated method provides a scientific foundation for stability assessment and dynamic remediation planning under complex hydrogeological conditions, offering a risk-informed and scenario-specific application of existing tools that improves engineering applicability. Full article