Search Results (928)

This work reports the rapid aqueous microwave-assisted synthesis of monoclinic scheelite BiVO₄ nanoparticles and their behavior under visible light. X-ray diffraction (XRD) confirms phase-pure BiVO₄ with an average crystallite size of ~19 nm, consistent with transmission electron microscopy (TEM) observations, while N₂ sorption yields a BET surface area of 7.5 m²/g. UV–Vis diffuse reflectance spectroscopy (DRS) indicates a direct band gap of 2.55 eV. We evaluated the effects of catalyst dosage and initial Acid Orange 7 (AO7) concentration on visible-light degradation efficiency. Up to 77% removal was achieved within 120 min, with kinetics following a pseudo-first-order model (R² ≈ 0.970–0.996). Under the tested conditions, BiVO₄ also exhibited a modest antibacterial effect against Escherichia coli (~0.5 log reduction). These findings demonstrate that microwave-synthesized BiVO₄ is a multifunctional material and provides a quantitative baseline for practical wastewater treatment studies under visible light. Full article

Basolite^® F300 and synthetic nano-{Fe-BTC} MOFs, two iron-trimesate MOFs, have been investigated, demonstrating broad pH range adsorption for monomethylarsenate (MMA), cacodylic acid (DMAA), 4-aminophenylarsonate (ASA), and arsenate, while arsenite adsorption was notable at pH > 9.5. A similar uptake trend was found for both MOFs, with Basolite^® F300 being the more effective given its higher porosity and greater surface area. Pseudo-second-order kinetic models were followed by MMA, DMAA, ASA, and As(V), suggesting a chemisorption mechanism with arsenic species diffusion into MOF pores as the controlling step. Equilibrium data for DMAA and ASA fit the Langmuir model whereas MMA adsorption fits the Redlich–Peterson model. The uptake of MMA, DMAA, and ASA by both Fe-MOFs is mainly attributed to their coordination with Fe(III). Aromatic units in ASA enhance adsorption through П-П stacking interactions. The competition between all arsenic species for the sorption sites of the Fe-MOFs led to an uptake decrease of 10% for MMA and ASA and higher than 30% for DMAA and As(V) with respect to the individual uptakes. The Fe-MOFs can be reused for four cycles by washing with acidic methanol. Basolite^® F300 and synthetic nano-{Fe-BTC} effectively removed organic and inorganic arsenic species, exhibiting rapid adsorption, selective uptake, stability, and easy regeneration. Full article

Mitigating climate change through the reduction of atmospheric CO₂ emissions remains a critical global priority. Solid adsorbents, particularly shales, have become promising options for CO₂ storage due to their favorable structural and chemical properties. In this study, a solid sorbent was developed by pyrolyzing shale at 800 °C under a nitrogen (N₂) atmospheric condition, yielding spent shale. The key physicochemical properties influencing CO₂ sorption were characterized using X-ray diffraction (XRD), Field Emission Scanning Electron Microscopy (FESEM), Brunauer–Emmett–Teller (BET) surface area analysis, and Temperature-Programmed Desorption (TPD). Mineralogical analysis revealed the presence of quartz, feldspars, clays, and carbonate minerals. The spent shale exhibited surface areas of 30–34 m²/g and pore diameters ranging from 3 to 10 nm. TPD results confirmed the presence of active adsorption sites, with a maximum CO₂ sorption capacity of about 1.62 mmol/g—surpassing several commercial sorbents. Adsorption behavior was best described by the Sips and Toth isotherm models (R² > 0.99), indicating multilayer and heterogeneous adsorption processes. Kinetic modeling using both pseudo-first-order and pseudo-second-order equations revealed that CO₂ uptake was governed by both diffusion and chemisorption mechanisms. These findings positioned spent shale as a low-cost, efficient sorbent for CO₂ storage, promoting circular resource utilization and advancing sustainable carbon management strategies. This novel shale-derived material offers a competitive pathway for carbon capture, storage, and sequestration applications. Full article

Graft copolymers of polysaccharides with side chains of carbon-chain monomers have significant potential for a variety of practical applications. In this work, the effect of the N,N-methylenebisacrylamide (MBA) introduction stage and acrylamide concentration in microwave-assisted radical copolymerization with xanthan gum on the structure and sorption properties of the cross-linked graft copolymer was studied. It has been found that the spatial network density and average molecular weight of interstitial fragments can be controlled by varying these factors. Moderate crystallinity (<50%) and a highly developed surface of our synthesized samples were revealed using XRD and SEM. The graft copolymer exhibits the Schroeder effect; its liquid water sorption obeys Fick’s law and increases with MBA introduction at later stages and with increasing grafting degree, reaching 17.2 g/g. Studying the methylene blue sorption kinetics using pseudo-first/pseudo-second order models, a combined model and an average pseudo-order model have shown that the lower the monomer concentration in the reaction mixture and the earlier (from the onset of the reaction) the cross-linking agent is introduced, the higher the equilibrium sorption. The observed “equilibrium degree of sorption on xanthan gum vs. pseudo-order” relationship, which passes through a minimum, is explained by chemisorption and the sorbate consumption effect. An assumption is made about the prospects of using our synthesized copolymers for designing selective sorbents and ion-exchange membranes. Full article

Activated carbons were synthesized from coffee grounds using phosphoric acid as a chemical activator and microwave-assisted carbonization as a rapid and energy-efficient method. Then the prepared carbons were surface-treated with cold plasma to improve their chemical properties and adsorption efficiency. The structural properties and chemical structure of the carbons were determined using nitrogen adsorption–desorption analysis, X-ray photoelectron spectroscopy, as well as X-ray microanalysis by means of scanning electron microscopy. The effect of cold plasma treatment on surface functionality and porosity was investigated. The resulting activated carbons were tested for their potential use as sorbents for the removal of ciprofloxacin, a commonly used antibiotic, from aqueous solutions. The effects of solution pH, sorption kinetics, and initial concentration were investigated. Adsorption kinetics followed a pseudo-second-order model, and the equilibrium data were well described by both the Langmuir and Freundlich isotherms, indicating a combination of monolayer adsorption on homogeneous sites and multilayer adsorption on heterogeneous surfaces. Plasma-treated carbon demonstrated significantly increased adsorption capacity (42.6–120.6 mg g⁻¹) compared to the unactivated samples (20.2–92.4 mg g⁻¹). Desorption experiments revealed that the plasma-treated carbon retained over 90% efficiency after seven cycles, confirming its excellent reusability and regeneration potential for practical water treatment applications. Full article

A novel magnetic composite, Fe₃O₄@MIL-53(Fe Cu), was successfully synthesized and applied for the efficient removal of methyl orange (MO) from aqueous solutions. The ad sorption performance was systematically evaluated under various conditions, including adsorbent dosage, solution pH, coexisting anions, and regeneration cycles. The results demonstrated that an optimal dosage of 20 mg achieved a removal efficiency exceeding 85%, with maximum adsorption observed at pH 3. The presence of common anions (Cl⁻, SO₄²⁻, CO₃²⁻, and PO₄³⁻) showed negligible effects on MO removal. Kinetic studies revealed that the adsorption process followed the pseudo-second-order model. Although minor chemisorption contributions were observed, the Dubinin–Radushkevich (D–R) model confirmed the predominance of physical adsorption. The Freundlich isotherm provided the best fit to the equilibrium data, indicating a maximum adsorption capacity of 193.65 mg/g and suggesting multilayer adsorption on a heterogeneous surface. Thermodynamic analysis confirmed the spontaneous and endothermic nature of the adsorption process. The primary mechanisms governing MO adsorption were identified as electrostatic attraction, π–π interactions, and hydrogen bonding. The composite exhibited excellent reusability over multiple cycles, demonstrating its potential for practical wastewater treatment applications. Full article

Biodegradable composites obtained by reinforcing thermoplastic starch (TPS) with lignocellulosic fibers show great potential, but their strong sensitivity to water still limits practical applications. Among possible reinforcements, Helianthus tuberosus (topinambur) represents an underutilized agricultural residue that has been scarcely explored in this context. In this work, we demonstrate for the first time that topinambur fiber can improve the water vapor barrier properties of cassava starch films, while also providing a detailed analysis of sorption isotherms and the humidity-dependent relationship between surface roughness and contact angle, aspects rarely addressed in previous studies. SEM revealed uniform fiber dispersion and integration. Water sorption kinetics showed that fiber addition reduces both hydration and sorption time constant, indicating lower water affinity and greater water mobility. Water sorption isotherms confirmed that fiber incorporation significantly alters overall hydration and water–matrix interactions, revealing reduced effective water solubility in films. Water vapor permeability also decreased with fiber addition, mainly due to decreased water solubility, rather than changes in water diffusivity. While fiber addition enhanced surface-water repellency across all humidity levels, roughness exhibited a humidity-dependent response FTIR analysis confirmed fiber–matrix compatibility and suggested new hydrogen bonding. Overall, these findings identify topinambur fiber as a novel reinforcement for designing biodegradable films with improved humidity resistance for agroecological applications. Full article

The influence of stress on gas sorption behavior and sorption-induced swelling in coal is critical for the success of CO₂-enhanced coalbed methane recovery (CO₂-ECBM) and geological carbon sequestration—a key strategy for mitigating climate change and promoting clean energy transitions. However, this influence remains insufficiently understood, largely due to experimental limitations (e.g., overreliance on powdered coal samples) and conflicting theoretical frameworks in existing studies. To address this gap, this study systematically investigates the effects of two distinct stress constraints—constant confining pressure and constant volume—on CO₂ adsorption capacity, adsorption kinetics, and associated swelling deformation of intact anthracite coal cores. An integrated experimental apparatus was custom-designed for this study, combining volumetric sorption measurement with high-resolution strain monitoring via the confining fluid displacement (CFD) method and the confining pressure response (CPR) method. This setup enables the quantification of CO₂–coal interactions under precisely controlled stress environments. Key findings reveal that stress conditions exert a regulatory role in shaping CO₂–coal behavior: constant confining pressure conditions enhance CO₂ adsorption capacity and sustain adsorption kinetics by accommodating matrix swelling, thereby preserving pore accessibility for continuous gas uptake. In contrast, constant volume constraints lead to rapid internal stress buildup, which inhibits further gas adsorption and accelerates the attainment of kinetic saturation. Sorption-induced swelling exhibits clear dependence on both pressure and constraint conditions. Elevated CO₂ pressure leads to increased strain, while constant confining pressure facilitates more gradual, sustained expansion. This is particularly evident at higher pressures, where adsorption-induced swelling prevails over mechanical constraints. These results help resolve key discrepancies in the existing literature by clarifying the dual role of stress in modulating both pore accessibility (for gas transport) and mechanical response (for matrix deformation). These insights provide essential guidance for optimizing CO₂ injection strategies and improving the long-term performance and sustainability of CO₂-ECBM and geological carbon storage projects, ultimately supporting global efforts in carbon emission reduction and sustainable energy resource utilization. Full article

The removal of nickel from industrial wastewater necessitates efficient sorbent materials. This study investigates nanostructured potassium- and sodium-substituted aluminosilicate-based nanocomposites for this application. Materials were synthesized and characterized using SEM-EDS, XPS, XRD, FTIR, low temperature N₂ adsorption–desorption and Ni²⁺ adsorption experiments. SEM and XRD confirmed an X-ray amorphous structure attributable to fine crystallite size. The sodium-substituted material Na₂Al₂Si₂O₈ exhibited the lowest specific surface area (48.3 m²/g) among the tested composites. However, it demonstrated the highest Ni(II) sorption capacity (64.6 mg/g, 1.1 mmol/g) and the most favorable sorption kinetics, as indicated by a Morris-Weber coefficient of 0.067 ± 0.008 mmol/(g·min¹/²). Potassium-substituted analogs with higher Si/Al ratios showed increased surface area but reduced capacity. Analysis by XPS and SEM-EDS established that Ni(II) uptake occurs through a complex mechanism, involving ion exchange, surface complexation, and chemisorption resulting in the formation of new nickel-containing composite surface phases. The results indicate that optimal sorption performance for Ni(II) is achieved with sodium-based aluminosilicates at a low Si/Al ratio (Si/Al = 1). The functional characteristics of Na₂Al₂Si₂O₈ compare favorably with other silicate-based sorbents, suggesting its potential utility for wastewater treatment. Further investigation is needed to elucidate the precise local coordination environment of the adsorbed nickel. Full article

Hybrid polysaccharide-based aerogels offer significant potential as advanced drug delivery platforms due to their tunable structure, high porosity, and biocompatibility. In this study, aerogel microparticles were synthesized using alginate, pectin, carrageenan, and their hybrid formulations via an emulsion–gelation technique followed by supercritical fluid CO₂ extraction. The resulting aerogels exhibit mesoporous structures with specific surface areas ranging from 324 to 521 m²/g and pore volumes between 1.99 and 3.75 cm³/g. Comprehensive characterization (SEM, gas sorption, XRD, TGA, DSC, and FTIR) confirmed that hybridization improved morphological uniformity and thermal stability compared to single polymer aerogels. Ibuprofen was used as a model drug to evaluate loading efficiency and release kinetics. Among all formulations, the alginate/carrageenan (2:1) hybrid showed the highest drug loading efficiency (93.5%) and a rapid release profile (>90% within 15 min), closely matching the performance of commercial ibuprofen tablets. Drug release followed Fickian diffusion, as confirmed by the Korsmeyer–Peppas model (R² > 0.99). These results highlight the potential of hybrid polysaccharide aerogels as vehicles for drug delivery and other fast-acting therapeutic applications. Full article

Thermochemical energy storage (TCES) has gained significant attention as a high-capacity, long-duration solution for renewable energy integration, yet material-level challenges hinder its widespread adoption. This review for the first time systematically examines recent advancements in nano-engineered composite thermochemical materials (TCMs), focusing on their ability to overcome intrinsic limitations of conventional systems. Sorption-based TCMs, especially salt hydrates, benefit from nano-engineering through carbon-based additives like CNTs and graphene, which enhance thermal conductivity and reaction kinetics while achieving volumetric energy densities exceeding 200 kWh/m³. For reversible reaction-based systems operating at higher temperatures (250–1000 °C), the strategies include (1) nanoparticle doping (e.g., SiO₂, Al₂O₃, carbonaceous materials) for the mitigation of sintering and agglomeration; (2) flow-improving agents to enhance fluidization; and (3) nanosized structure engineering for an enlarged specific surface area. All these approaches show promising results to address the critical issues of sintering and agglomeration, slow kinetics, and poor cyclic stability for reversible reaction-based TCMs. While laboratory results are promising, challenges still persist in side reactions, scalability, cost reduction, and system integration. In general, while nano-engineered thermochemical materials (TCMs) demonstrate transformative potential for performance enhancement, significant research and development efforts remain imperative to bridge the gap between laboratory-scale achievements and industrial implementation. Full article

Background/Objectives: The principal function of pharmaceutical blister packaging is to provide protection for the drug product. Moisture is regarded as a critical factor in the physical and chemical aging of drug products. The present work proposes a modeling framework to predict the performance of tablet blister materials based on the moisture uptake profile of the drug product as well as degradation characteristics of the drug substance, while the consumption of water due to degradation is included. Methods: The model incorporates three kinetic superimposed processes that define moisture uptake and drug stability. The processes of permeation, sorption and degradation are each described with a rate constant. Based on a mass balance, these rate processes are interconnected and the relative humidity in the blister cavity is predicted. Results: In a case study, the model was applied to demonstrate the feasibility of predicting the stability of blistered tablets. By establishing a correlation between the moisture uptake of the tablet and the drug stability demonstrated in the model, it was feasible to predict the drug content over shelf life. Conclusions: Modeling of the drug stability of blister-packed products enables a rational packaging which offers novel possibilities for reducing material in order to avoid overpackaging of pharmaceutical products. As some of the commonly used barrier materials are considered to not be sustainable, this model can be used to consider a rationally justified reduction or even abandonment of the barrier materials. Full article

This study reports the production of carbon adsorbents via microwave-assisted chemical activation of caraway seeds using potassium carbonate (K₂CO₃). Microwave irradiation enables rapid, energy-efficient heating, promoting effective pore development at relatively low activation temperatures (400–600 °C). The resulting carbons were comprehensively characterized in terms of surface area, pore structure, and surface chemistry, and their adsorption performance was evaluated for both cationic (methylene blue) and anionic (methyl red) dyes. The adsorbents exhibited specific surface areas ranging from 25 to 634 m²/g, with sorption capacities up to 217 mg/g for methylene blue and 171 mg/g for methyl red. Adsorption kinetics followed a pseudo-second-order model, and isotherm analysis revealed that Langmuir adsorption predominates for methylene blue, while Freundlich adsorption better describes methyl red uptake, reflecting surface heterogeneity. This work demonstrates that caraway seeds are a low-cost, sustainable precursor for producing microwave-activated carbons and provides new insights into the influence of activation temperature and surface chemistry on dye adsorption mechanisms, highlighting the practical potential of these materials for wastewater treatment applications. Full article

In this study, a commercial anion-exchange resin (D301), known for high regenerability but limited selectivity, was chemically modified to enhance its sorption performance. The modification included graft polymerization of glycidyl methacrylate followed by thiourea functionalization, yielding a new sorbent, TD301, with chelating functional groups. Characterization using SEM/EDS, IR spectroscopy, XPS, and zeta potential measurements confirmed the successful introduction of sulfur- and nitrogen-containing groups, increased surface roughness, and decreased surface charge in the pH range 2–6. These changes shifted the sorption mechanism from nonspecific ion exchange to selective coordination. Sorption properties of TD301 were evaluated in mono- and bimetallic Mo–W systems, as well as in solutions obtained from real ore decomposition. The modified sorbent showed fast sorption kinetics and high selectivity for Mo(VI) at pH 1.5, while retaining high W(VI) uptake at pH 0.5. In binary systems, separation factors (α) reached 128.4, greatly exceeding those of unmodified D301. In real leachates (Mo ≈ W ≈ 0.04 g/L), TD301 selectively extracted W at pH 0.66 and Mo at pH 1.5. These findings demonstrate that TD301 is an effective sorbent for pH-dependent Mo/W separation in complex matrices, with potential for resource recovery, wastewater treatment, monitoring, and suitability for repeated use. Full article

In this study, red mud (RM) was utilized as an iron and aluminum source, and reed biomass served as a carbon precursor to prepare red mud-modified biochar beads (RM/CSBC) via the gel-calcination method. Under a pyrolysis temperature of 900 °C and an RM/biomass dosage of 3 g each, RM/CSBC exhibited an optimal balance between adsorption performance and cost. Within typical pH range of 6–9 in wastewater, RM/CSBC maintained effective adsorption performance, while metal ion leaching (Fe ≤ 0.3 mg·L⁻¹, Al ≤ 0.2 mg·L⁻¹) complied with Class II surface water standards in China. Kinetic data were well fitted by the pseudo second-order model, supported by the Elovich model, indicating the involvement of both chemical and physical adsorption mechanisms. Isotherm results showed that the Langmuir model provided the best fit, indicating monolayer adsorption, with a maximum capacity of 85.16 mg·g⁻¹ at 25 °C. XPS analysis revealed the formation of AlPO₄ and FePO₄ precipitates, confirming chemical precipitation as a key mechanism, along with electrostatic attraction and physical sorption. This study highlights the feasibility of RM/CSBC as an efficient and low-cost phosphate adsorbent and provides a theoretical basis for phosphorus removal and recovery from wastewater using waste-derived materials. Full article