Search Results (972)

Sunset Yellow is a water-soluble synthetic dye resistant to degradation and stable under various conditions, posing an environmental challenge. In the present study pure chitosan hydrogel (PCH) films were synthesized, followed by the assessment of sorption capacity and recyclability compared to chitosan-based films doped with niobium oxide (CHN) or activated carbon (CHC). The aim was to promote the application of sorption methods for Sunset Yellow dye using these films as a treatment option for the pollutant, with the analysis of the effectiveness of the method and its behavior using adsorption kinetic models and thermodynamic analysis. Equilibrium was reached at 240 min for all films tested, with the adsorbed amounts ranging from 18.58 to 18.79 mg g⁻¹ at 30 °C, when the highest kinetic rate constants were observed. The pseudo-first-order kinetic model best described the experimental data, with the lowest Bayesian information criterion, Akaike information criterion, and mean absolute error values. Thermodynamic analysis indicated a spontaneous, exothermic process, with interactions ranging from electrostatic interactions in CHC and PCH to physisorption in CHN. Recycling tests showed 80% efficiency after the third cycle for all three films. These findings highlight the potential of chitosan-based films as an efficient option for removing Sunset Yellow dye from water, thus improving water quality and enhancing wastewater treatment. Full article

Fungal decay fundamentally alters moisture transport in wood through complex bio-physical coupling mechanisms that remain poorly understood. Brown-rot fungi such as Coniophora puteana (Schumach.: Fr.) P. Karst. degrade wood through chelator-mediated Fenton (CMF) chemistry, producing hydroxyl radicals that depolymerise cellulose and hemicellulose before significant mass loss. This diffusion-dependent process requires elevated moisture content and leads to structural degradation. However, existing models fail to capture the interaction between boundary-driven fungal colonization, decay-induced property changes, and multi-phase multi-Fickian moisture redistribution, particularly the separate evolution of bound- and free-water phases during decay. Here, we present a transport-response bio-hygrothermal finite element model that couples boundary-driven Monod-type fungal colonization kinetics with multi-phase moisture transport (free water, bound water, vapor) in decaying wood. Although fungal biomass evolution is simulated via a reaction–diffusion equation, decay progression is not derived from biomass–substrate interaction but prescribed independently as an experimentally informed input. The model incorporates decay-modified sorption isotherms, permeability evolution, and boundary-driven biomass influx, along with associated moisture transport, into the governing equations. The model is validated against low-field nuclear magnetic resonance (LF-NMR) measurements of C. puteana decay in Scots pine over 35 days. The model successfully reproduces the experimentally observed moisture evolution: a peak free-water content of 50%–70% during weeks 1–2, followed by a progressive decline, while bound water remains remarkably constant despite advancing decay. Monte Carlo uncertainty quantification demonstrates hierarchical parameter control: bound water is governed solely by thermodynamic factors, while free water responds to interacting biological and physical processes. Time-resolved correlation analysis shows a fundamental transition from colonization-dominated (weeks 1–2) to transport-dominated (weeks 3–5) moisture control, quantitatively explaining the experimentally observed shift from accumulation to depletion. This transport-response framework for analyzing moisture behavior under externally defined decay progression establishes quantitative parameter hierarchies that may inform the development of future substrate-coupled bio-hygrothermal models. Full article

Depletion of reserves of rich copper–porphyry ore deposits necessitates the development of highly efficient methods for Mo (VI) extraction from complex, corrosive hydro-metallurgical media. The present study undertakes a comprehensive assessment of sorptive concentration of Mo (VI) from strongly acidic sulfate solutions (120 g/L H₂SO₄) by employing a spectrum of commercially available strong- and weak-base anion-exchange resins. It has been established that the macroporous weak-base anion exchanger Purolite A-100 demonstrates decisive superiority over gel-type analogs (Lewatit M-800, AB-17), facilitating unimpeded intra-gel diffusion of bulky molybdenyl sulfato-complexes anions, thereby circumventing the obstructive “sieve effect.” Thermodynamic and kinetic investigations revealed that the sorption process exhibits pronounced concentration- and pH-dependent characteristics. Peak extraction efficiency (up to 95.91%) is achieved at pH ≈ 1, a finding that correlates with the region of maximal protonation of tertiary amino groups within the resin matrix. Kinetic acceleration of mass transfer upon heating to 80 °C has been experimentally confirmed, yielding 94.6% extraction within 60 min. The obtained results corroborate the prospective integration of macroporous weak-base anion exchangers into operational hydro-metallurgical schemes as an environmentally benign and efficacious alternative to conventional solvent extraction of molybdenum. Full article

Steroid hormones (SHs) have a high estrogenic potential, and urban wastewater is one of their main ways into the aquatic environment. Constructed wetlands (CWs) are considered one of the most sustainable alternatives for the treatment of wastewater from small communities. However, the use of gravel and sand implies a significant environmental impact associated with their extraction and transport. A more sustainable alternative is the use of plant residues, as they are abundant, inexpensive, and readily available, and they can improve the efficiency of hormone removal through sorption. Thus, the sorption of 15 SHs was studied on conventional, mineral substrates (gravel, sand, and volcanic ash) and alternative vegetal wastes, i.e., mulches from giant reed, palm tree, balsa wood, and pine needles. These materials were characterized by determining their Point of Zero Charge (pH_PZC), ash content, content of leachable polycyclic aromatic hydrocarbons (PAH) and heavy metals, total surface area (BET), and pore characteristics. Results indicated that SH sorption on the mineral substrates was quite low, in most cases less than 10–15%. However, in the mulches it reached between 50 and 95%, except for corticosteroids (11–43%). The pseudo-second-order kinetics provided the best fit in all cases, with R² values between 0.97 and 0.9999. Experiments with a contact time of 7 days showed that the palm tree was the only substrate that completely removed the three corticosteroids studied (cortisone, prednisone, and prednisolone). Additionally, a significant correlation was observed between removal due to sorption (%) and log octanol–water partition coefficient (log Kow). Freundlich isotherm provided a higher number of best fits than Langmuir. Lastly, to compare sand with palm mulch under more realistic experimental conditions, four lab-scale CWs (two with palm mulch and two with sand, with/without plants) were studied. The sand-based CWs achieved faster SH percentage removals, while after 24 h, SH mass removals were significantly higher in the palm mulch-based CWs. Full article

This study investigated the application of apricot stone, an agro-industrial by-product, as a sustainable biosorbent for the removal of Zn ions from aqueous solutions and industrial galvanic wastewater. The equilibrium data conformed well to the Sips isotherm model, indicating heterogeneous sorption behavior, and revealed a maximum sorption capacity of 58.2 mg/g. The biosorbent exhibited a high initial removal efficiency of 95% in aqueous Zn solutions, while its performance in real industrial wastewater was reduced to 55%, due to matrix interference. Ecotoxicological test using seed germination assays revealed no phytotoxic effects from the Zn-loaded sorbent. These findings demonstrate that apricot stone is an effective, low-cost, and environmentally friendly sorbent with significant potential for application in Zn-contaminated water treatment systems, contributing to circular economy and waste valorization initiatives. Full article

Biopolymers such as chitosan are considered important candidates for water purification due to their non-toxicity, biodegradability, natural origin, biocompatibility, and potential for modification to provide additional capabilities, such as incorporating nanomaterials for magnetism to enable rapid separation or adding functional groups to enhance selectivity towards target adsorbates. This study investigated adsorption of Co (II), traced by Co-60 radionuclide, systematically evaluated in natural aquatic matrices selected according to water body type: seawater (Baltic Sea) and freshwater systems further distinguished as lentic (Lake Balsys) and lotic (Neris River) environments, using synthesized magnetite–chitosan nanocomposites (MCNs) with varying loadings of Fe₃O₄ (10–30 wt. %) nanoparticles providing different levels of magnetization. Comprehensive characterization (TEM, FTIR, AFM, XRD, and Mössbauer spectroscopy) confirmed successful integration of magnetite nanoparticles within the chitosan matrix and reproducible structural properties. An optimal magnetization of 11 emu/g was achieved at 20 wt. % Fe₃O₄, enabling rapid magnetic separation within <1 min without compromising sorption capacity. Adsorption isotherm models were applied to investigate the adsorption parameters, and sorption kinetics were studied, yielding a maximum adsorption capacity of 14.93 mg/g for MCN-10 in seawater and 11.95 mg/g for MCN-20 in freshwater with observed equilibrium within 120 min. These promising results indicate that the MCN is a suitable nanocomposite for the removal of Co (II) ions and the Co-60 radionuclide from aquatic media. Full article

This paper investigates the effectiveness of a coal mine methane drainage system in hard coal mining, with particular emphasis on coal seam 501 at the Staszic–Wujek coal mine (Polska Grupa Górnicza S.A., Katowice, Poland) in the Upper Silesian Coal Basin (USCB), Poland. The study evaluates methane drainage efficiency considering geo-mechanical conditions governing the optimal location of drainage boreholes. Conventional and long directional boreholes are analyzed. Opposite to conventional static analytical approaches, the proposed integrated analysis framework incorporates multi-physics processes, improving forecasting accuracy and enabling dynamic optimization of methane control in deep coal mines. The framework reproduces the geometry of the mining system and the mechanical properties of the surrounding rock mass, allowing the influence of geo-mechanical processes on methane drainage efficiency to be assessed. The methane content of coal seam 501 and methane sorption kinetics on representative coal samples are analyzed together with key characteristics of the mine ventilation system, including air and pressure distribution in workings and goafs and migration paths of methane–air mixtures within coal panel II/C. Full article

The objective of this study was to develop a predictive methodology for assessing the leakage phenomenon of gelatin-based soft capsules under various storage conditions. The equilibrium moisture content of the soft capsules was influenced by the temperature and humidity. The leakage phenomenon was attributable to the swelling of gelatin, as revealed by Fourier Transform Infrared spectroscopy (FT-IR) and Scanning Electron Microscopy (SEM) imaging techniques. Additionally, the moisture diffusion mechanism of soft capsule shells was systematically investigated based on the principles of hygroscopic kinetics, enabling quantitative evaluation of their hygroscopic performance under different environmental conditions. Based on macromechanical analysis, the mechanical failure curves of soft capsule shells under different environmental conditions were investigated, enabling successful determination of the shelf life of the soft capsules. Importantly, the Arrhenius equation and the generalized Eyring model were introduced to successfully predict the occurrence of leakage during storage. The developed prediction method performs successful and accurate stability assessment under various conditions, which is crucial for the development of soft capsules. Full article

A comprehensive study was conducted to determine the suitability of biochar produced from agricultural waste in the form of alfalfa (BL₅₀₀) and corn (BC₅₀₀) for methylene blue (MB) adsorption. As part of the research, biochar was produced at 500 °C by pyrolysis using a CO₂ atmosphere. BL₅₀₀ and BC₅₀₀ biochar were characterised in terms of their physicochemical and structural properties using FTIR spectroscopy, Raman spectroscopy, and N₂ adsorption–desorption. The produced biochars are characterised by a significant ash content and high carbon content. They have a specific surface area of 4.12 m²/g (BL₅₀₀) and 19.84 m²/g (BC₅₀₀), a micro-mesoporous structure and are rich in functional groups (including OH, COOH, CO). BL₅₀₀ biochar showed greater effectiveness in removing methylene blue (MB) than BC500, with maximum sorption capacities of 39.94 mg/g and 19.47 mg/g, respectively. Furthermore, kinetic model fitting indicated that the adsorption process follows a pseudo-second-order model and a Langmuir monolayer model. However, the intramolecular diffusion model (IPD) and Bangham models confirmed that the adsorption process does not occur in a single stage. The produced biochar can be used as a sustainable adsorbent for MB from aqueous solutions. Full article

This study investigated how fabrication method (milling versus 3D printing) affects the water sorption and solubility of PMMA dental materials, and how surface characteristics affect hydrolytic stability. Fifty-six PMMA samples were divided into three groups fabricated from CAD/CAM milled discs (Group A: I–III) and four groups from 3D-printed resin (Group B: IV–VII), each subjected to distinct postprocessing protocols. Water sorption (wsp) and solubility (wsl) were measured after immersion in distilled water at 37 °C for 24, 48, and 72 h, and 7 and 14 days. Surface topography and nanoroughness were assessed using atomic force microscopy (AFM). Statistical descriptive analyses were followed by correlation analyses. Milled PMMA demonstrated significantly lower water sorption and negative solubility (mass loss), indicating material dissolution. In contrast, 3D-printed PMMA showed higher water sorption and positive solubility (mass gain), reflecting water incorporation and polymer swelling. The kinetic profiles differed: milled PMMA displayed a monophasic absorption curve, while 3D-printed PMMA exhibited a biphasic pattern with accelerated water uptake after 72 h. AFM analysis revealed that 3D-printed surfaces had significantly greater nanoroughness than milled surfaces. Strong positive correlations were observed between surface roughness parameters (Sa, Sy) and water sorption capacity. The fabrication method was found to influence the hydrolytic stability of PMMA dental materials. Milled PMMA demonstrated superior stability, with lower water uptake, smoother surfaces, and lower leaching solubility. In contrast, 3D-printed PMMA exhibited increased surface roughness and water sorption, attributed to its layered microstructure and nanoporosity. Surface topography emerged as a strong predictor of wsl, related to hydrolytic degradation. For clinical applications, milled PMMA is recommended for long-term use requiring durability, whereas 3D-printed PMMA may be appropriate for short-term applications with optimised postprocessing. Full article

Boron nitride is considered a promising material for solid-state hydrogen storage due to its high thermal and chemical stability up to ~1000 °C, depending on the atmosphere, as well as its ability to form defect-rich structures with enhanced sorption activity. Despite the growing interest in modified BN systems, systematic studies on the effect of multicomponent modification induced by the addition of carbon, titanium, and aluminum on the structural and phase evolution of boron nitride during high-energy mechanical alloying remain limited to date. In this work, the structural-phase and morphological changes in boron nitride-based composites modified by the addition of carbon, titanium, and aluminum, synthesized by high-energy mechanical alloying, were investigated. The structural state and morphology of the materials were analyzed using X-ray diffraction, scanning electron microscopy, particle size analysis, and thermal analysis. It is shown that mechanical alloying leads to a progressive breakdown of the layered hexagonal BN structure and the formation of an amorphous-like, defect-rich state without the formation of new crystalline phases. The main stage of amorphization occurs within 30–60 min, after which structural disordering reaches saturation. Increasing the mechanical alloying time to 120 min does not result in significant changes in the phase state; however, it is accompanied by a reduction in agglomeration and the formation of a more homogeneous powder morphology, characterized by narrower particle size distributions, smoother particle surfaces, and more uniform spatial dispersion of components. It was established that the nature of the added component significantly influences the kinetics of structural transformations: carbon accelerates amorphization, titanium intensifies fragmentation and defect accumulation, whereas aluminum exhibits a stabilizing effect. In multicomponent BN–C–Ti–Al systems, a synergistic combination of these effects is observed, leading to the formation of metastable, partially amorphous structures. Based on a comprehensive analysis of structural and morphological data, the optimal mechanical alloying time was determined to be 120 min, providing a saturated amorphous-like structural state combined with improved microstructural homogeneity. The obtained defect-rich boron nitride structures can be considered a promising basis for further studies in the field of solid-state hydrogen storage. Full article

Polycyclic aromatic hydrocarbons (PAHs) can enter water bodies and bioaccumulate in fish, leading to biomagnification; therefore, their monitoring is necessary. Passive sampling is easy to handle and shows potential for this purpose. However, studies in vivo are scarce, and kinetic parameters governing analyte partitioning between tissue and samplers remain poorly characterized. In this study, the silicone rubber membranes (SRMs) were exposed to fish fillet from common carp (Cyprinus carpio) to determine bioaccumulation parameters based on dissipation modelling using performance reference compounds (PRCs). The SRM was implanted in vivo in fish, and the dissipated PRCs were measured and applied to a mono-compartmental model. The results in fish fillet showed a pseudo-first kinetic order, and the plateau was attained at a time > 30 h. However, the equilibrium may not be ensured because of the low lipid fraction (fl) in fish (4.5%), which could lead to a local saturation of the tissue in contact with the SRM. The ratio between elimination and uptake constants (K_e/K_u) showed faster PAHs–SRM sorption than PAHs-fish tissue sorption (200 times); thus, fish with low fl will lead to faster SRM sorption. By contrast, in fish with higher fl, the long-term exposures will be necessary. The percentage of released deuterated PAHs from SRM during in vivo fish exposure was 1.6 times higher than that observed in the fish fillet, indicating an active clearance process. Therefore, during implantation, the rate of clearance and the fl should be considered to ensure detectable levels for applying the integrative equation based on dissipation modelling. Full article

This study evaluates the impact of a comprehensive design integrating precursor type, reduction and freeze-casting on the development of aerogels with high sorption capacity for engine oil. In this respect, the graphene oxide was varied from commercial to expanded; the reduction approach relied either on purely hydrothermal or combined hydrothermal–chemical reduction approaches. Following the synthesis, freeze-casting was applied at −5 °C and −196 °C. To further improve the reduction degree, annealing in an inert atmosphere was employed upon drying. The effects of precursors, reduction approach, freeze-casting and annealing were systematically investigated. Characterization techniques, including FT-IR, Raman spectroscopy, SEM, and EDS, were used to correlate the degree of reduction and morphological features of the porous structure with the absorption properties. The use of expanded GO as a precursor yielded aerogels with more homogeneous three-dimensional networks, a reduced bulk density of 3 mg cm⁻³, and lower oxygen-containing functional group content, thereby achieving consistently superior oil absorption of 270 g g⁻¹, with an oil occupancy of 94%. The process was found to fit well with the pseudo-first-order kinetic model. The results demonstrate that a comprehensive approach—considering combined reduction, freeze-casting, and thermal annealing—enables the tailored optimization of both the structure and absorption performance of GO aerogels for the remediation of oil spills. Full article

In this study, magnetic porous glycidyl methacrylate and ethylene glycol dimethacrylate copolymer (mP) grafted with tetraethylenepentamine (mP-TEPA) obtained in a two-step procedure was tested as the CO₂ sorbent. The morphological, textural, structural, and thermal characterization of the sample was determined by scanning electron microscopy with energy-dispersive X-ray analysis (SEM-EDS), mercury intrusion porosimetry (MIP), nitrogen physisorption at 77 K, Fourier transform infrared spectroscopy in ATR mode (FTIR-ATR), X-ray photoelectron spectroscopy (XPS), elemental analysis, and thermogravimetric analysis (TGA). The effects of thermodynamic and kinetic parameters, as well as the adsorption/desorption mechanism on the CO₂ sorption ability of mP-TEPA, were investigated using a pulse gas chromatographic method. Under optimal adsorption conditions, the CO₂ sorption capacity reached 6.20 mmol CO₂/g (6.20 × 10⁻² mmol CO₂/m²). Temperature-programmed desorption (TPD) experiments were conducted to calculate the activation energy of CO₂ desorption. The low desorption activation energy of 18.80 kJ/mol and high desorption rate, with stable CO₂ uptake after ten adsorption/desorption cycles, suggest that mP-TEPA is a potentially excellent sorbent for CO₂ adsorption. Full article

This review presents a modern comprehensive analysis of the physicochemical characteristics of carbon materials for the sorption of gases. The main classes of carbon sorbents are considered as follows: nanotubes, activated carbon, graphene, fullerene, composite materials, and organic vapors. Modern methods of modification of carbon materials are systematized. Particular attention is paid to the effect of particle size, morphology, and porous structure on the kinetics and equilibrium characteristics of adsorption. The results of experimental and theoretical studies of the adsorption of the gases (CO₂, SO₂, NO_x, H₂S, NH₃, and CO) are analyzed. A comparative economic analysis of carbon materials is carried out, taking into account the cost of production and estimated costs of modification. Modern areas of application of carbon sorbents are analyzed as follows: industrial gas purification, automotive filters, air conditioning systems, personal protective equipment, and gas sensors. Particular attention is paid to the study of the prospects and future of materials. Prospective development directions are considered, including the creation of hierarchically porous structures, the development of self-healing materials, and integration with artificial intelligence to optimize adsorption processes. The cost of graphene and nanotube production is predicted to decrease by 50–70% by 2030, which will lead to an expansion of their commercial application. Full article