Search Results (2,135)

Thorium (Th) is increasingly considered a promising fertile material for sustainable nuclear energy—which is not fissile itself, but convertible to fissile ²³³U—particularly as a by-product of rare earth element (REE) processing. This study develops a parametric techno-economic assessment (TEA) framework synthesizing published data from China, Russia, the USA, India, and Europe to establish the methodological foundation for evaluating thorium recovery economics from monazite ores and REE tailings under Central Asian conditions. Monazite typically contains 4–12% ThO₂, while tailings contain 0.1–3%, making secondary resources attractive for future recovery strategies. Particular attention is given to integration with uranium tailings and the application of advanced materials such as nanocomposite sorbents and carbon-based electrodes. Reported production costs of ThO₂ range from 50 to 500 USD/kg depending on process scale, feedstock quality, and co-production of REEs. The reviewed studies consistently show that coupling thorium recovery with REE processing improves economic feasibility. Modern approaches, including hybrid technologies and electrosorption systems, may reduce operational costs and improve process efficiency. Despite challenges related to capital investment, market uncertainty, and radioactive waste management, thorium continues to attract growing interest as a potential component of future nuclear fuel cycles and advanced reactor systems, including small modular reactors. To the best of the authors’ knowledge, this is the first parametric TEA framework structured around Central Asian conditions, combining literature-derived regional data, scenario-based process economics, and Monte Carlo sensitivity analysis within a single discounted cash flow structure. Full article

Fine-dispersed gold is difficult to quantify in natural and technogenic materials because it may occur as micron- and submicron-sized particles, films, inclusions, sorbed forms, and matrix-bound species. This study aims to provide a scientific basis for a two-stage methodology designed for the separate assessment of gravity-recoverable and hidden forms of gold. The proposed workflow includes gravity separation, ultrasonic aerohydraulic desliming, controlled thermal activation with a carbonaceous sorbent, low-temperature HCl-HNO₃-HF acid digestion at 98 °C for 2 h, instrumental Au determination, statistical processing, and SEM-EDS verification. The studied materials included ores, weathering crusts, placer materials, gravity tailings, ash-slag waste, thermally treated products, and sorbents. Two analytical series, each consisting of 50 Au determinations, showed high heterogeneity, with Au contents ranging from 0.10 to 2.80 g/t and from 0.0259 to 5.0330 g/t, respectively. Gravity-separation balance data showed that a substantial proportion of Au may remain in the tailings. SEM-EDS revealed microheterogeneity, porous aggregates, microspheres, and candidate phases; however, it was used only for mineralogical verification rather than as a quantitative method for total Au determination. The proposed workflow improves the informativeness of hidden Au-form assessment and requires further laboratory standardization. Full article

The Baleysky gold deposit in Eastern Transbaikalia is a classic example of the long-term environmental legacy of gold mining. The cessation of industrial wastewater discharge in 1995 led to the accumulation of more than 3 million m³ of acidic water with high concentrations of heavy metals and metalloids. These waters contain concentrations many times higher than the maximum permissible levels for fishery waters (Mn up to 6594, Al—1473, Zn—486, and Cu—414), posing a significant threat to the ecosystem of the Unda River and the health of the local population. The aim of this study was to evaluate the effectiveness of the artificial geochemical barrier method for treating such waters under laboratory conditions. Column experiments were conducted using local soil and the commercial carbonate sorbent taurite at a sorbent-to-filtrate ratio of 1:5. Taurite demonstrated a significantly higher sorption capacity than soil, substantially reducing the concentrations of As, Cd, Pb, Al, Mn, Fe, Zn, and Cu and raising the pH from 2.90 to 7.96–8.03. Although health risks associated with both carcinogenic (CR) and non-carcinogenic effects (HI) decreased significantly after treatment with taurite, residual risk levels remained unacceptably high (CR ≈ 10⁻³, HI > 1). The results show that engineered geochemical barriers have great potential for reducing anthropogenic contamination at abandoned mining sites, although further optimization of this technology is necessary to achieve compliance with regulatory requirements. Full article

Oil spills represent a critical environmental challenge. The wastewater treatment with porous sorbents presents the advantage of higher uptake and recyclability. In this work, highly porous and low-density three-dimensional reduced graphene oxide aerogels were obtained by hydrothermal reduction followed by lyophilization. The porosity and reduction degree of the aerogels were controlled by the addition of reducing species, namely ethylenediamine, and hydrothermal conditions. The aerogels were characterized using scanning electron microscopy, Raman spectroscopy, and energy-dispersive X-ray analysis. The sorption measurements were performed with vegetable oils, namely canola and olive oil, at varying operating temperatures. The morphological analysis revealed a well-defined porosity gradient along the aerogel length, along with a functionalization gradient. The sorption performance is highly dependent on their combined action. The maximum gravimetric absorption capacity was about 122 g g⁻¹ at room temperature, increasing to 156 g g⁻¹ at 60 °C, with the absorption rate increasing from about 1 g g⁻¹ s⁻¹ to 15 g g⁻¹ s⁻¹ within 10 s. These results demonstrate that anisotropic gradient aerogels could be obtained by simple tailoring of the synthesis conditions, and such aerogels could benefit the sorption of oils with higher viscosities in terms of rate, pore filling and retention. Full article

Environmental pollution by polycyclic aromatic hydrocarbons (PAHs) is a serious environmental problem. One of the effective methods of cleaning the environment from these toxicants is the use of sorbents based on clay minerals. Special organo-mineral, bio-mineral and bio-organo-mineral complexes were obtained. Organo-mineral complexes (organoclays) were synthesized on the basis of Na-bentonite and anionic, amphoteric and nonionic surfactants. Bio-mineral and bio-organo-mineral complexes were produced by inoculating bentonite and organoclays with a consortium of bacteria. The adsorption characteristics of the complexes to benzopyrene and naphthalene were studied. Modification of bentonite with various types of surfactants leads to a significant increase in the percentage adsorption of both benzopyrene and naphthalene, with benzopyrene being more so. All bio-organo-mineral complexes adsorb more benzopyrene than pure bentonite and the bentonite + bacteria complex. In most cases, this pattern is also characteristic of naphthalene adsorption. Organoclay complexes with bacteria adsorb PAHs in greater quantities than organoclays, typically at the average concentrations of benzopyrene and naphthalene used (30–60 μg mL⁻¹) and when modified with individual surfactants. Based on the determination coefficients, the adsorption of benzopyrene and naphthalene by all studied sorbents is best described by the Langmuir equation. The maximum (limiting) adsorption of benzopyrene by all organo-mineral complexes (organoclays) exceeds the maximum adsorption of benzopyrene by bentonite. Modification of bentonite with surfactants may not change, decrease, or increase the maximum adsorption of naphthalene compared to the original bentonite, depending on the surfactant used. Colonization of the organoclay surface by bacteria, with rare exceptions, results in a decrease in the maximum adsorption values of benzopyrene and naphthalene compared to organoclay, or has no effect at all. Full article

Metanephrine (MN) and normetanephrine (NMN) are critical biomarkers for neuroendocrine tumors (pheochromocytoma and paraganglioma). Following our previous development of a molecularly imprinted solid-phase extraction (MISPE) sorbent for urine analysis, this study evaluated MISPE coupled with HILIC-MS/MS for determining metanephrines in human plasma. Unlike conventional phases, the novel polymer selectively binds analytes as in situ-generated anions via quaternary alkylammonium groups in hydroxide form, ensuring accurate extraction from just 25 µL of plasma. Validated per U.S. FDA guidelines, the assay showed good intra- and interday precision (CV < 10.8%), accuracy (bias < −10.6%) and excellent linearity (R² > 0.99) across pathological ranges (184.3–877.8 ng/L for MN; 174.8–923.0 ng/L for NMN), with low relative standard errors (<6.9%). Excellent selectivity was demonstrated in the presence of structurally close analogs (catecholamines, DOPA and its derivatives). Compared with commercial WCX, the sorbent yielded cleaner extracts, significantly reducing the phospholipid interference. Although lower limits of quantification (92.2 ng/L MN; 87.4 ng/L NMN) slightly exceeded healthy upper thresholds, the method has potential for use in specific clinical scenarios with pronounced biomarker elevations: diagnosis of pheochromocytoma/paraganglioma, monitoring post-treatment metanephrine decline, and tracking tumor-induced hypertensive crises in emergencies. This accessible protocol forms a solid foundation for advanced diagnostics. Full article

Amid growing pressure to reduce carbon emissions, carbon capture, utilization, and storage (CCUS) has become an important pathway toward deep decarbonization. However, the conventional separated “capture–release–conversion” process suffers from high energy consumption and system complexity, which severely limits its large-scale application. Integrated CO₂ Capture and Utilization (ICCU), which enables the capture, activation, and conversion of CO₂ within a single system, has attracted widespread attention because it can effectively reduce intermediate energy-intensive steps and improve carbon utilization efficiency. This review systematically summarizes recent progress in ICCU technology, with particular emphasis on reaction mechanisms and interfacial coupling characteristics. The performance features of solvent-based chemical absorption and solid-sorbent adsorption, two widely studied capture routes, are summarized, and typical integrated conversion pathways, including reverse water–gas shift, methanation, and dry reforming of methane, are discussed. On this basis, the roles of non-conventional energy-assisted strategies, such as photocatalysis, electrocatalysis, non-thermal plasma, and microwave irradiation, in expanding ICCU systems are further examined, together with their system-level coupling potential in carbon-intensive industries such as steel, cement, and power generation. Finally, the key scientific issues and engineering challenges currently facing ICCU are analyzed from the perspectives of fundamental mechanisms, material design, and system engineering, and future development directions are proposed. This review highlights that elucidating multiscale synergistic mechanisms, developing high-performance dual-function materials, and optimizing system integration are crucial to promoting the industrial application of ICCU technology. Full article

Biomass pellets and briquettes are commonly treated as compacted solid biofuels, but their potential extends beyond direct combustion and heat generation. This review aims to synthesise current knowledge on pellets and briquettes as both energy carriers and functional materials for agro-environmental, biological, sorption, and material applications. A structured narrative review was conducted using Web of Science, Scopus, and OpenAlex, complemented by targeted searches of standards, life-cycle assessment studies, and recent experimental literature. This review discusses key physicochemical, mechanical, and environmental properties, including density, moisture content, durability, ash content, higher heating value, elemental composition, storage stability, and biodegradability. It also compares major energy pathways, including combustion, combined heat and power, torrefaction, hydrothermal carbonisation, pyrolysis, and gasification, with non-combustion uses such as fertiliser and microbial carriers, sorbents, bedding materials, mushroom substrates, biocomposites, and lightweight building components. Published studies indicate that the environmental performance of densified biomass depends strongly on feedstock origin, drying energy, transport, end-use technology, and system boundaries. The review proposes a quality-to-function framework in which pellet and briquette quality is interpreted in relation to the intended application rather than through a single universal fuel-quality criterion. This approach supports more precise biomass valorisation within circular bioeconomy systems. Full article

Hierarchical ZnO–SiO₂/carbon composites (C-Zn1, C-Zn2, C-Zn3) were synthesised via the carbonisation of resorcinol–formaldehyde gels in the presence of ZnO-modified fumed silica, and characterised by N₂ adsorption–desorption, FTIR, XRD, SEM, and zeta potential analysis. The composites exhibited hierarchical micro–mesoporous structures with BET surface areas of 467–499 m² g⁻¹; the non-microporous volume fraction increased from 0.09 (reference carbon RFC, 545 m² g⁻¹) to 0.54–0.63 upon ZnO–SiO₂ incorporation. Adsorption of methylene blue (MB), crystal violet (CV), and rhodamine 6G (R6G) followed the Marczewski–Jaroniec isotherm model. Maximum adsorption capacities for the best-performing composite (C-Zn1) reached 1.22 mmol g⁻¹ for MB, 1.04 mmol g⁻¹ for CV, and 0.63 mmol g⁻¹ for R6G, compared to 1.32, 1.17, and 0.67 mmol g⁻¹ for unmodified RFC. Kinetic analysis revealed up to 3.5-fold faster adsorption rates for C-Zn1 relative to RFC (for CV and R6G), attributed to enhanced diffusion through mesoporous channels while preserving the micropore-driven capacity. Agar well-diffusion assays against four bacterial strains showed no inhibition zones for any composite, indicating that no biologically active concentration of zinc species was released under the assay conditions. The proposed approach yields composites with enhanced adsorption kinetics, preserved capacity, and confirmed non-leaching character, positioning them as effective candidates for water purification. Full article

The production of inexpensive, effective sorbents from natural materials for the purification of water bodies and/or soils is a pressing problem. Therefore, the purpose of this manuscript is to summarize current approaches to the use of brown coal (lignite) and its processing products (humic acids, HAs) as sorbents for the purification of aqueous and soil environments from heavy metal ions and other pollutants. Modification of lignite (chemical, biological, physicochemical) or the creation of lignite–mineral composites significantly increases its sorption capacity and stability: after modification, the sorption capacity can reach more than 85 mg of heavy metals per g of sorbent, which is only 3 times lower than that of specialized, expensive sorbents. Also, good results are achieved in the case of sorption of water-soluble organic drugs, dyes, etc. Humic acids obtained from brown coal have better selectivity and efficiency than the original lignite, and slightly worse than the modified one, in terms of removing cadmium, lead, copper, and other toxic elements; and also, can complex with organic xenobiotics. Current research trends indicate growing interest in multifunctional composite sorbents, environmentally friendly extraction technologies, and the development of materials with enhanced selectivity and regeneration ability. Future studies should focus on improving the understanding of sorption mechanisms, optimizing modification strategies, scaling up lignite-based technologies for practical environmental applications, and developing waste-free technologies to produce sorbents from lignite. Full article

This study investigates the potential of several sustainable agricultural by-products—including olive stones, cork, and almond shells, which are locally available in Alentejo, Portugal—as low-cost adsorbents for the removal of methylene blue (MB) from synthetic wastewater. The biomass residues were evaluated both in their raw form and after conversion into activated carbons (ACs) through chemical activation with KOH at 973 K. The produced ACs exhibited well-developed surface areas (760–1103.5 m² g⁻¹) and porous structures (0.31–0.51 cm³ g⁻¹). The adsorbents were characterised in terms of their chemical and textural properties. Raw biomass materials presented acidic surface groups, whereas the ACs presented neutral or basic groups. Batch adsorption experiments were conducted to assess the effects of adsorbent particle size, solution pH, initial MB concentration, stirring speed, contact time, and temperature on dye removal efficiency. Among all tested materials, the ACs achieved superior MB adsorption capacities, ranging from 244.2 to 317.6 mg g⁻¹, compared to the untreated biomass adsorbents, which showed capacities between 34.1 and 46.4 mg g⁻¹. The adsorption data were best described by the Langmuir isotherm model, while the kinetic data closely followed the pseudo-second-order (PSO) model. Thermodynamic analysis revealed that MB adsorption was spontaneous and endothermic; however, the relatively low enthalpy values indicated that physical interactions contributed significantly, particularly in the case of the raw biomass adsorbents. This suggests that the PSO model may also be applicable when physical adsorption is the dominant mechanism. This work demonstrates the novel use of cork, olive stone, and almond shell biomasses and their derived ACs as sustainable adsorbents, highlighting an integrated approach that simultaneously promotes efficient wastewater treatment, waste valorisation, and circular economy-driven socio-economic development. Full article

The scientific literature lacks sufficient data on the transport of various toxic pollutants by polymer particles. Investigating how the structure of microplastic particles formed during the degradation of polymeric materials affects pollutant sorption processes will improve our ability to predict environmental behavior. General-purpose polystyrene, expanded polystyrene, ABS plastic (acrylonitrile–butadiene–styrene) and crosslinked polystyrene are produced on an industrial scale. Copolymers of styrene with divinylbenzene are used on a large scale as sorbents for gel permeation chromatography (Styragel brand sorbents), in the production of catalysts on a polymer substrate or ion-exchange resins. In this study, non-spherical, crosslinked polystyrene microparticles with varying polystyrene chain packing densities were used as model microplastic particles representative of crosslinked polystyrene. It was shown that the adsorption of a hazardous chemical rhodamine B was influenced by both the packing density of the polystyrene chains and the presence of ionic functional groups, i.e., the “degree of aging” of the microplastic particles. The sorption capacities of these model microparticles were compared with those of natural origin (silicon dioxide, quartz powder, and microcrystalline cellulose). A viability assay using HEK293 and HeLa cell lines exposed to leachates from both pristine and rhodamine B-loaded microparticles revealed that all unmodified microparticles, regardless of their nature, exhibited no cytotoxicity at concentrations up to 1000 μg/mL. In contrast, microparticles with adsorbed rhodamine B significantly reduced cell viability to 20–40% at concentrations of 100 μg/mL. Full article

Bentonite is widely used as a sorbent due to its high specific surface area and ion-exchange capacity; however, its properties can be significantly influenced by the presence of additional mineral phases and chemical modification. In this study, the influence of manganese oxides and quartz sand on the sorption properties of bentonite from the Stará Kremnička was systematically investigated, with particular attention to surface characterization by X-ray photoelectron spectroscopy (XPS). The materials were also characterized by X-ray diffraction, FTIR spectroscopy, and zeta potential measurements. XPS analysis revealed that manganese in all modified samples was predominantly present in the Mn(IV) oxidation state, with Mn 2p₃/₂ binding energies of 642.5–642.7 eV, corresponding to MnO₂-type phases. Deconvolution of the O 1s spectra confirmed the presence of lattice oxygen, silicate oxygen, and surface hydroxyl groups. The reason for the modification of mainly natural materials with manganese oxides is their higher affinity for the adsorption of heavy metal cations. The maximum adsorption capacity of natural bentonite was 63.29 mg/g. In bentonite samples modified with manganese oxides, the value increased to 103.09 mg/g for BMn, and to 116.28 mg/g for the MMn mixture. The results demonstrate that sorption behavior is governed by a combination of ion exchange on bentonite and interactions with Mn oxide surface phases, providing new insight into the role of Mn(IV) species in surface-controlled metal binding processes. These findings highlight the importance of surface chemical states in designing efficient bentonite-based sorbents. Full article

For the removal of hexavalent chromium [Cr(VI)] from drinking water, a hybrid biosorbent designated chitosan–natural diatomaceous earth (CNDE) was developed and thoroughly characterized. The material couples the ion-exchange and chelating capacity of chitosan—applied at an 85% degree of deacetylation—with the high-surface-area mineral framework of natural diatomaceous earth, onto which the polymer was deposited as a conformal coating. Surface morphology and internal microstructure were examined by scanning and transmission electron microscopy (SEM/TEM), while elemental composition across the hybrid matrix was resolved by energy-dispersive X-ray spectroscopy (EDX). Fourier transform infrared (FTIR) spectroscopy was employed to identify the surface functional groups responsible for chromate binding, and streaming current measurements established the pH of zero charge (pH_pzc), which governs the electrostatic environment at the sorbent–solution interface. Specific surface area was quantified by the Brunauer–Emmett–Teller (BET) method, and the balance of surface acidic and basic sites was determined through titrimetric analysis of total acidity and alkalinity. Thermogravimetric analysis (TGA) was conducted to assess thermal stability. Batch equilibrium isotherm experiments were performed to evaluate Cr(VI) uptake from model drinking water prepared using dilute potassium dichromate solutions adjusted to target pH levels. The effects of solution pH and competing anions (chloride and sulfate) were also investigated. Kinetic studies were conducted to determine the rate of Cr(VI) adsorption, and residual metal concentrations were measured using inductively coupled plasma mass spectrometry (ICP-MS). Results indicated that CNDE containing 30% chitosan (CNDE30) achieved effective Cr(VI) removal at pH 5. Adsorption was strongly pH-dependent, decreasing as pH increased from 5 to 8. Equilibrium data were well described by both Langmuir and Freundlich isotherm models, while kinetic data followed a pseudo-second-order model. The presence of chloride ions (15 mg/L) reduced adsorption capacity by approximately one-third, whereas sulfate at the same concentration significantly inhibited Cr(VI) removal. Overall, the isotherm results suggest that CNDE30 is a promising material for Cr(VI) removal from drinking water. Its cost-effectiveness, ease of synthesis, and potential for reuse make it particularly attractive for small-scale and decentralized water treatment applications. Full article

Cellulose-based materials have been widely investigated as sustainable sorbents for oil spill remediation due to their renewability, biodegradability, low density, and structural diversity. However, reported performance varies substantially across material classes, modification strategies, and testing conditions, making direct comparison difficult. This review summarizes recent progress in cellulose-based sorbents for oil removal, with emphasis on the relationships between processing methods, pore architecture, surface wettability, and sorption behavior. Native cellulose materials, chemically modified cellulose, aerogels, nanocellulose-based systems, and carbonized cellulose are comparatively discussed in terms of oil uptake, selectivity, sorption kinetics, retention stability, reusability, and mechanical performance. The analysis indicates that sorption efficiency is controlled by the combined effects of hierarchical porosity, surface characteristics, and structural integrity. Native materials provide low cost and rapid uptake but limited selectivity, whereas chemically modified systems show improved hydrophobicity and oil retention. Aerogels generally exhibit some of the highest reported absorption capacities but often suffer from low mechanical durability. Nanocellulose-based materials generally offer a balanced combination of sorption capacity and stability, while carbonized materials typically provide enhanced retention at the expense of transport rate. Current limitations, including scalability, durability, and realistic operating conditions, are also discussed to outline future directions for the design of efficient cellulose-based oil sorbents. Full article