Search Results (605)

Simulation studies of adsorption in complex effluents are challenging due to nonlinear interactions between sorbents, adsorbates and carrying flows. This study investigates effluents from oil and textile industries, characterised by their heavy metal content and chemical oxygen demand. It examines the process in a continuous-flow laboratory-scale adsorption system. Results were validated using process modelling based on mass and energy conservation, applied to an industrial adsorber. The model described surface sorption mechanisms on bioactivated carbon at the molecular level and predicted breakthrough curve profiles, integrated with Aspen Plus ^® adsorption simulation under industrially relevant conditions. Experimental data and model predictions showed good agreement, with relative deviations ranging from 0.2% to 24.6%. Differences in adsorption capacities between oily and textile effluents highlighted the influence of coexisting constituents. At the same time, the varied behaviour of identical components supported the hypothesis of multifactorial effects in complex mixtures. The optimisation study, using Response Surface Methodology with a Central Composite design, evaluated factors such as bed height, feed rate, and adsorption cycle time, achieving enhanced removal efficiencies of 62% for chemical oxygen demand and 25% for suspended solids. Full article

Carbonaceous amendments are widely proposed to sequester hydrophobic organic contaminants in sediments, yet their effectiveness for alkylphenolic endocrine disruptors in organic-rich freshwater systems—and its time dependence—remains poorly constrained. Here, we compared activated carbon (AC), biochar (BC), and humic compost (HC) for reducing desorption and maize phytoexposure to 4-octylphenol (4-OP) and 4-nonylphenol (4-NP) in canal sediment from the Jegrička River. Sediment was spiked (~1.1 mg kg⁻¹ 4-OP; 1.2 mg kg⁻¹ 4-NP), amended with 0.5–10% (w/w) AC, BC, or HC, and aged for up to 180 days prior to multi-step XAD-4 desorption tests. A two-compartment first-order model resolved fast- and slow-desorbing pools, while a 10-day maize (Zea mays L.) pot experiment quantified early phytoextraction and sediment–plant–loss mass balances for AC and HC treatments. The unamended sediment exhibited high operational bioavailability: ~98% of both alkylphenols were XAD-4-extractable, and 83–89% of the desorbable pool was released within 24 h. AC produced the most rapid immobilization; at 0.5–1%, it halved XAD-4-extractable fractions within weeks and reduced them to near-zero within months, whereas BC and HC achieved comparable reductions only after longer aging. Plant uptake was a minor sink: in the control, shoots accumulated ~21 µg kg⁻¹ sediment of 4-OP and 65 µg kg⁻¹ sediment of 4-NP (≈2% and 5% of the initial inventory). HC generally lowered uptake, and high AC doses kept plant burdens consistently low. Overall, amendment-enhanced sorption and sequestration dominated attenuation, with AC delivering the fastest risk reduction and HC representing a more plant-compatible amendment option. Full article

Frequent crude oil spills during offshore oil and gas production and transportation have inflicted irreversible detrimental effects on both human activities and marine ecosystems; with particular risks of secondary disasters such as combustion and explosions. To address these challenges; advanced oil sorption technologies have been developed to overcome the inherent limitations of conventional remediation methods. In this study, a flame-retardant protective coating was fabricated on melamine sponge (MS) through precipitation polymerization of octa-aminopropyl polyhedral oligomeric silsesquioxane (POSS) and hexachlorocyclotriphosphazene (HCCP), endowing the MS@PPOS-PDMS-Si composite with exceptional char-forming capability. Secondary functional layer: By coupling the complementary physicochemical properties of polydimethylsiloxane (PDMS) and SiO₂ nanofibers, we enabled them to function jointly, achieving superior performance in the material systems; this conferred enhanced hydrophobicity and structural stability to the MS matrix. Characterization results demonstrated a progressive reduction in peak heat release rate (PHRR) from 137.66 kW/m² to118.35 kW/m², 91.92 kW/m², and ultimately 46.23 kW/m², accompanied by a decrease in total smoke production (TSP) from 1.62 m² to 0.76 m², indicating significant smoke suppression. Furthermore, the water contact angle (WCA) exhibited substantial improvement from 0° (superhydrophilic) to 140.7° (highly hydrophobic). Cyclic sorption–desorption testing revealed maintained oil–water separation efficiency exceeding 95% after 10 operational cycles. These findings position the MS@PPOS-PDMS-Si composite as a promising candidate for emergency oil spill response and marine pollution remediation applications, demonstrating superior performance in fire safety, environmental durability, and operational reusability. Full article

Emerging pollutants such as pharmaceuticals and synthetic dyes increasingly enter agricultural soils through irrigation with treated or untreated wastewater and via biosolid amendments, raising concerns for plant health, soil functionality, and food chain safety. Their environmental behavior is governed by complex interactions between compound physicochemistry, soil properties, and plant physiology, leading to variable persistence, mobility, and ecotoxicological outcomes. This review synthesizes current evidence on the fate, uptake, and phytotoxic effects of drug and dye contaminants in plant–soil systems, and provides a comparative assessment of ecological risks before and after photocatalytic wastewater treatment. The analysis integrates findings from soil- and hydroponic-based studies addressing pollutant sorption–desorption dynamics, leaching, microbial transformations, and plant responses ranging from germination impairment and biomass reduction to oxidative stress and genotoxicity. Special emphasis is given to the formation and behavior of transformation products generated during photocatalytic degradation, which may display altered mobility or toxicity relative to parent compounds. Comparative evaluation reveals that photocatalysis substantially reduces contaminant loads and toxicity in many cases, although incomplete mineralization or the formation of reactive intermediates can sustain or enhance adverse effects under certain conditions. By linking pollutant fate mechanisms with plant and soil responses, this review highlights both the potential and the limitations of photocatalysis as a sustainable strategy for safeguarding agroecosystems in the context of expanding wastewater reuse. Full article

The characterization and biomedical modification of bentonite clays from the Kalzhat deposit (Kzh), which is situated in Kazakhstan’s Zhetysu region, are the main objectives of this work. In order to improve the raw material’s structural qualities, the montmorillonite fraction was enriched, and coarse impurities were eliminated using the Salo method. The presence of meso- and micropores that guarantee high dispersity and specific surface area, as well as the prevalence of montmorillonite and kaolinite, was all confirmed by physicochemical analysis. Particle size measurements indicated finely dispersed structures with a propensity to aggregate, whereas thermal analysis demonstrated resilience under heating. After effective functionalization with silver nanoparticles, a porous hybrid system with improved surface reactivity was produced. These enhancements demonstrate the modified bentonite’s usefulness as a multifunctional carrier for the immobilization and controlled release of pharmaceuticals, with potential uses in drug delivery systems, antimicrobial coatings, and wound-healing materials. The material has potential use in sorption and environmental protection technologies in addition to its biomedical application. Overall, Kzh’s structural and functional performance is greatly improved by the combination of purification and functionalization with silver nanoparticles, highlighting its promise as a useful element in the development of next-generation polymer–composite systems. Full article

Guamuchil (Pithecellobium dulce) is an underutilized legume with significant potential as a food ingredient. This study valorized guamuchil fractions (pulp, peel, and seed) by developing dietary fiber concentrates (DFC) and evaluating their physicochemical, techno-functional, and antioxidant properties using a single-factor completely randomized design. Proximate composition and dietary fiber profiles (2011.25) were analyzed following AOAC official methodologies. Results showed the peel fraction contained the highest total dietary fiber (64.16 ± 1.23 g 100 g⁻¹ dry basis (db)) and total phenolic content (15.46 ± 0.26 mg GAE g⁻¹ db), positioning it as a bioactive fiber source. Conversely, the pulp DFC exhibited superior hydration properties, with high solubility (43.54 ± 1.22%), swelling (10.23 ± 0.30 mL g⁻¹ db), and water retention capacity (14.17 ± 0.35 mL g⁻¹ db), making it suitable as a texturizer. Moisture sorption isotherms exhibited type II sigmoidal behavior, accurately fitted by GAB and Peleg models (R² ≥ 0.997). The pulp showed higher hygroscopicity and water binding ability, whereas peel and seed fractions displayed lower sorption and enhanced stability. These findings demonstrate that Guamuchil DFCs are suitable as a potential food formulation ingredient owing to their high functionality. Full article

Combining different materials into binary salts can significantly enhance the efficiency and stability of Thermochemical Energy Storage (TCES) systems. This study aimed to develop and characterise novel salt hydrate composite materials for TCES, focusing on a mixture of magnesium chloride (MgCl₂) and calcium chloride (CaCl₂) impregnated into a mesoporous silica gel (SG) sphere matrix. Three different MgCl₂/CaCl₂ salt ratios were investigated to find the optimal balance between sorption capacity and stability against deliquescence in humid environments. Prepared samples underwent comprehensive characterisation, including structural and morphological analysis, water vapour sorption and heat capacity measurements. The hybrid CaCl15/MgCl15/SG sample exhibited intermediate behavior between the pure CaCl30/SG and MgCl30/SG samples, with significantly improved stability in a humid environment due to the addition MgCl₂. Characterisation revealed the effective confinement of the salt mix in the matrix. The optimised CaCl15/MgCl15/SG sample demonstrated highly promising gravimetric and volumetric energy storage capacities of 1092 J/g and 2.3 MJ/m³, respectively, comparable to recently reported composites. The material sorption dynamics were ultimately tested in a whole adsorbent unit under near-real-world operating conditions, pushing the research to the reactor and system level, and demonstrating that the presence of MgCl₂ in the composite does not adversely affect the adsorption kinetics compared to the pure CaCl₂-based composite. Full article

The sustainable operation of hydroponic systems depends on maintaining the chemical stability of circulating nutrient solutions and preventing the accumulation of toxic compounds. The accumulation of phytotoxic ammonium, heavy metals, and organic metabolites in recirculating nutrient solutions remains one of the key challenges limiting the efficiency, sustainability, and scalability of hydroponic cultivation. This review provides a comprehensive comparative analysis of zeolites, activated carbons (ACs), and their functionalized and composite forms as key sorbents for nutrient management, contaminant removal, and environmental safety in hydroponic cultivation. Natural zeolites, with their well-defined crystalline structure and high ion-exchange selectivity toward ammonium and heavy metal cations, enable effective NH₄⁺/K⁺ balance regulation and phytotoxicity mitigation. ACs, characterized by high specific surface area and tunable surface chemistry, complement zeolites by offering extensive adsorption capacity for organic compounds, root exudates, and pesticide residues, thereby extending the operational lifespan of nutrient solutions and improving overall system performance. Further advancements include the integration of zeolites and ACs with two-dimensional (graphene, g-C₃N₄) and three-dimensional (MOF, COF) frameworks, yielding multifunctional materials that combine adsorption, ion exchange, photocatalysis, and nutrient regulation. Transition-metal modification, particularly with Fe, Mn, Cu, Ni, and Co, introduces redox-active centers that enhance sorption, catalysis, and phosphate stabilization. The comparative synthesis reveals that the combined application of zeolite- and carbon-based composites offers a synergistic strategy for developing adaptive and low-waste hydroponic systems. From a techno-economic and environmental standpoint, the judicious application of these materials paves the way for more resilient, efficient, and circular hydroponic systems, reducing fertilizer and water consumption, lowering contaminant discharge, and enhancing food security. This systematic review was conducted according to the PRISMA 2020 guidelines. Relevant studies were identified through Scopus, Web of Science, and Google Scholar databases using specific inclusion and exclusion criteria. Full article

Studies have shown that natural organic matter can regulate pollutant behavior through multiple pathways; however, research on the environmental behavior of veterinary antibiotics (VAs) in typical alkaline calcareous loess soil under the influence of exogenous organic matter remains limited. This study investigated the influence of humic acid (HA), as a representative of natural organic matter, on the sorption behavior of ciprofloxacin (CIP) in sierozem—a typical alkaline calcareous loess soil. Using the batch equilibrium method, we examined how HA affects CIP sorption under various environmental conditions to better understand the environmental fate of VAs in soil–water systems with low organic matrix content. Results showed that CIP sorption onto sierozem involved both fast and slow processes, reaching equilibrium within 2 h, with sorption capacity increasing as HA concentration increased. Kinetic data were well described by the pseudo-second-order model regardless of HA addition, suggesting multiple mechanisms governing CIP sorption, such as chemical sorption reaction, intraparticle diffusion, film diffusion, etc. Sorption decreased with increasing temperature both before and after HA amendment, indicating an exothermic process. Isotherm analysis revealed that both the Linear and Freundlich models provided excellent fits (R² ≈ 1), implying multilayer sorption dominated by hydrophobic distribution. In ion effect experiments, cations at concentrations above 0.05 mol/L consistently inhibited CIP sorption, with inhibition strength following the order: Mg²⁺ > K⁺ > Ca²⁺ > NH₄⁺, and intensifying with increasing ionic strength. However, HA addition significantly mitigated this inhibition, likely due to complexation between HA’s functional groups (e.g., carboxyl and hydroxyl) and cations, which reduced their competitive effect and enhanced CIP sorption. pH-dependent experiments indicated stronger CIP sorption under acidic conditions. HA addition increased soil acidity, further promoting CIP retention. In summary, HA enhances CIP sorption in sierozem by providing additional sorption sites and modifying soil surface properties. These findings improve our understanding of how exogenous organic matter influences the behavior of emerging contaminants such as antibiotics in soil–water systems, offering valuable insights for environmental risk assessment in semi-arid agricultural regions. Full article

Wastewater-derived microplastics (WW-MPs) are increasingly recognised as reactive vectors for aromatic organic contaminants (AOCs), yet their role in contaminant fate remains insufficiently constrained. This review synthesises current knowledge on the transformation of microplastics in wastewater treatment plants, including fragmentation, oxidative ageing, additive leaching, and biofilm formation, and links these processes to changes in sorption capacity toward phenols, PAHs and their derivatives, and organochlorine pesticides (OCPs). We summarise the dominant adsorption mechanisms-hydrophobic partitioning, π-π interactions, hydrogen bonding, and electrostatic and, in some cases, halogen bonding-and critically evaluate how wastewater-relevant parameters (pH, ionic strength, dissolved organic matter, temperature, and biofilms) can modulate these interactions. Evidence in the literature consistently shows that ageing and biofouling enhance WW-MP affinity for many AOCs, reinforcing their function as mobile carriers. However, major gaps persist, including limited data on real wastewater-aged MPs, lack of methodological standardisation, and incomplete representation of ageing, competitive sorption, and non-equilibrium diffusion in existing isotherm and kinetic models. We propose key descriptors that should be incorporated into future sorption and fate frameworks and discuss how WW-MP-AOC interactions may influence ecological exposure, bioavailability, and risk assessment. This critical analysis supports more realistic predictions of AOC behaviour in wastewater environments. Full article

Biodegradable bioplastics have emerged as a promising sustainable alternative to minimize the environmental impact of traditional plastics. Nevertheless, many of them degrade slowly under natural or industrial conditions, raising concerns about their practical biodegradability. This fact is related to the high-order structure of the polymer backbones, i.e., high molar mass and high crystallinity. Research efforts are being devoted to the development of technologies capable of reducing the length of polymer segments by accelerated chain scission, which could help improve biodegradation rates upon disposal of bioplastic products. The objective of this review is to examine the current state of the art of abiotic degradation techniques, physically driven by temperature, mechanical stress, UV/gamma/microwave irradiation, or plasma or dielectric barrier discharge, and chemically induced by ozone, water, or acidic/basic solutions, with the aim of enhancing the subsequent biodegradation of bioplastics in controlled valorization scenarios such as composting and anaerobic digestors. Particular attention is given to pretreatment degradation technologies that modify surface properties to enhance microbial adhesion and enzymatic activity. Technologies such as ozonation and plasma-driven treatments increase surface hydrophilicity and introduce functional groups with oxygen bonds, facilitating subsequent microbial colonization and biodegradation. Irradiation-based techniques directly alter the chemical bonds at the polymer surface, promoting the formation of free radicals, chain scission, and crosslinking, thereby modifying the polymer structure. Pretreatments involving immersion in aqueous solutions may induce solution sorption and diffusion, together with hydrolytic chain breakage in bulk, with a relevant contribution to the ulterior biodegradation performance. By promoting abiotic degradation and increasing the accessibility of biopolymers to microbial systems, these pretreatment strategies can offer effective tools to enhance biodegradation and, therefore, the end-of-life management of bioplastics, supporting the transition toward sustainable cradle-to-cradle pathways within a biocircular economy. Full article

Iron deficiency anemia continues to pose a significant global health burden, necessitating the development of improved therapeutic delivery systems. This study investigates novel composite materials composed of organosilicon hydrogels and cross-linked sulfobutyl ether beta-cyclodextrin (SBECD) nanoparticles for the oral delivery of iron compounds. Two types of cross-linked SBECD nanoparticles were synthesized using 1,6-hexamethylene diisocyanate. These nanoparticles were characterized by DLS, NTA, and FTIR and possess size around 200–300 nm and negative zeta-potential around −35 mV with molecular weight 150–200 kDa. Various hydrogel matrices, including plain PMSSO hydrogels and modified versions with amino groups or silicate cross-links, are also described. The hydrogels were evaluated for their iron sorption capacity (up to 44% loading efficiency) and release kinetics for 3 h. The results demonstrate that cross-linked SBECD nanoparticles significantly enhance iron sorption and provide sustained release under simulated physiological conditions. Mathematical modeling indicated that the Higuchi model best describes the iron release kinetics. The findings suggest that the proposed composite materials hold considerable promise for the treatment of iron deficiency anemia, offering an innovative approach to enhance therapeutic efficacy and minimize adverse effects. Full article

This paper presents a new study and analysis of the thermo-hygroscopic behavior of Arthrospira platensis using dynamic vapor sorption (DVS) system. Thermo-hygroscopic characterization is essential for optimizing the drying process and enhancing storage conditions. Therefore, the objective of this work was to investigate the thermo-hygroscopic properties of Arthrospira (Spirulina) platensis using a dynamic vapor sorption (DVS) system. This thermo-hygroscopic analysis focused on three fundamental parameters, namely: the desorption isotherms, the net isosteric heat of water desorption, and the moisture diffusivity. Desorption isotherms were measured at five different temperatures (25 °C, 40 °C, 50 °C, 60 °C and 80 °C) over a relative humidity range of 10–80%. The desorption isotherm data were fitted to five semi-empirical models: GAB, Oswin, Smith, Henderson, and Peleg. The results indicated that the GAB model provided the best fit for the experimental data. The net isosteric heat of desorption was determined using the Clausius–Clapeyron relation. It decreased from 21.3 to 4.29 KJ/mol as the equilibrium moisture content increased from 0.02 to 0.1 Kg/Kg (dry basis). Additionally, the moisture diffusivity of Arthrospira platensis was estimated based on Fick’s second law of diffusion and the desorption kinetics obtained from the DVS equipment. This parameter varied between 1.04 10⁻⁸ m²/s and 1.46 10⁻⁷ m²/s for average moisture contents ranging from 0.003 Kg/Kg to 0.191 Kg/Kg (dry basis). Furthermore, the activation energy for desorption was estimated to be approximately 33.7 KJ/mol. Full article

The sorption, structural, and thermal properties of the interpolymer system based on polymethacrylic acid (PMAA) and poly-4-vinylpyridine (P4VP) were studied at different component ratios for the extraction of rhenium (ReO₄⁻) and molybdenum (${\mathrm{M}\mathrm{o}\mathrm{O}}_4^{2-}$) ions from model solutions. The results showed that sorption efficiency depends on both composition and contact time. Systems with molar ratios of 3:3 and 2:4 exhibited the highest activity, reaching more than 90% extraction for rhenium and up to 94% for molybdenum after 48 h. FTIR spectra indicated the involvement of carboxyl and pyridine groups in complex formation with the metal ions, as evidenced by band shifts and the appearance of new absorption features. Thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) demonstrated that modification of PMAA with P4VP enhances the thermal stability of the system, which is maintained even after desorption. The system with the optimal composition showed structural stability and the ability to regenerate without a notable decrease in sorption capacity. Sorption performance was preserved across a wide pH interval, with maximum values at pH 2–4, which makes the system suitable for hydrometallurgical applications. Comparison with literature data indicates agreement with current approaches to rare-metal recovery, while the PMAA–P4VP system is distinguished by improved stability and potential for further development. These findings provide a basis for the design of selective and environmentally safe processes for rhenium and molybdenum recovery, relevant to the conditions of the Republic of Kazakhstan, where technogenic solutions rich in these metals are available. Full article

The industrial application of CO₂ methanation in Power-to-X (P2X) systems requires the development of highly active catalysts capable of operating at milder temperatures to ensure energy efficiency, while exhibiting high activity, stability and selectivity. This study reports the synthesis and optimization of Ni-based catalysts on Al₂O₃ supports, guided by a Design of Experiments (DoE, 2⁴ factorial design) approach. Initial optimization afforded a robust catalyst achieving 80% CO₂ conversion and >99% CH₄ selectivity at 325 °C. Remarkably, the incorporation of CeO₂ traces to the Ni-based catalyst substantially boosted catalytic activity, enabling higher conversions at temperatures up to 75 °C lower than the unpromoted catalyst. This improvement is attributed to Ni–CeO_x synergy, which facilitates CO₂ activation and Ni reducibility. Both formulations exhibited exceptional long-term stability over 100 h. Furthermore, process intensification via the Sorption-Enhanced Reaction Process (SERP) with the Ni-based catalyst demonstrated even superior efficiency, rapidly increasing CO₂ conversion beyond 95% with the same selectivity range. Our findings establish a clear and consistent pathway for industrial CO₂ valorization through next-generation P2X technology for high-purity synthetic natural gas (SNG) production. This process offers an efficient and sustainable route toward industrial defossilization by converting captured CO₂ and green H₂ into SNG that is readily usable within the existing energy infrastructure. Full article