Search Results (635)

Metal hydrides can safely store hydrogen in the solid state at high volumetric density under moderate temperature and pressure. Their hydrogen sorption characteristics are represented by pressure–composition–temperature (PCT) curves. AB₅–type metal hydrides, which have low plateau pressures, store and release hydrogen at low pressures. AB₂–type metal hydrides, which have high plateau pressures, store and release hydrogen at relatively high pressures. Compared with AB₅–type metal hydrides, AB₂–type metal hydrides generally have lower raw material costs and higher hydrogen storage capacity. This makes them more suitable for storing large quantities of hydrogen. Green and blue hydrogen are produced using commercial alkaline water electrolyzers and natural gas reformers, respectively. After downstream purification, this hydrogen is typically supplied at pressures below 1 MPa. However, the high plateau pressures of AB₂–type metal hydrides make it difficult to store this low-pressure hydrogen directly. AB₅–type metal hydrides can store it but release it only at low pressures. A single hydride type therefore operates within a narrow pressure range for both storage and delivery. In this study, a multipurpose hydrogen storage system (MHSS) using AB₅– and AB₂–type metal hydrides was proposed to broaden the applications of metal hydride-based systems. The feasibility of the MHSS was experimentally evaluated through lab-scale tests. The AB₅ and AB₂ modules were first tested as standalone units. The integrated MHSS was then tested assuming that waste heat was continuously available. The MHSS can store a large quantity of low-pressure hydrogen and deliver it across a wide pressure range. This range covers diverse end uses, from fuel cells at 0.5 MPa to hydrogen pipelines at 4.0 MPa. 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

Earth-based materials are promising candidates for balancing thermal performance, hygrothermal regulation, and environmental sustainability. The objective of this study is to evaluate and compare the hygrothermal behavior of two earthen materials, structural cob and lightweight insulating earth, against conventional reference concrete, taking into account not only their insulating properties but also their ability to regulate coupled heat and moisture transfers. Experimental tests show a significantly higher hygroscopic buffering capacity for earth-based materials, with an MBV of 2.23 g/(m²∙%RH) for the structural material and 1.21 g/(m²∙%RH) for the insulation material, compared to less than 0.5 g/(m²∙%RH) for concrete. The sorption isotherms confirm distinct water storage behaviors, with an average sensitivity to relative humidity of 10.47% for the insulation material, compared to 3.8% for concrete and 2.25% for the structural material, in addition to an average reduction of 26% in the adsorption capacity between 23 °C and 45 °C for both earthen materials. Coupled heat–moisture simulations in COMSOL quantitatively demonstrate the hygrothermal superiority of bio-based materials over conventional concrete, as concrete promotes interstitial moisture accumulation due to its low vapor permeability. The parametric sensitivity analysis highlights the effect of hygrothermal properties, where diffusivity controls transport kinetics and sorption governs water storage, while thermal conductivity modulates the spatial redistribution of thermo-hygric fields. The next and final step made it possible to link the phenomena observed at the material scale to the actual energy performance of the building, confirming the potential of the double-wall cob + lightweight earth system to reduce heating and cooling requirements and maintain stable indoor comfort, where the annual heating demand is reduced by approximately 24% compared to the conventional prototype. Full article

The sorption behavior of antibiotics in wastewater treatment systems plays a critical role in determining their environmental fate and removal efficiency. In this study, the sorption of 15 antibiotics representing multiple classes was investigated using two sewage sludge samples with different physicochemical characteristics. Batch equilibrium experiments were conducted to evaluate time-dependent sorption behavior and to determine solid–water distribution coefficients (K_d). The results showed that sorption occurred rapidly, with most compounds approaching a stable concentration within 24 h. The K_d values varied widely depending on the compound, ranging from 74 to 737 L/kg. For 13 of the 15 investigated antibiotics, higher K_d values were observed in sludge B than in sludge A, with the largest difference observed for tiamulin (402 ± 53 and 737 ± 76 L/kg for sludge A and sludge B, respectively). Sludge B generally exhibited higher sorption capacity for most compounds than sludge A, despite having a lower specific surface area, indicating that sorption was governed primarily by chemical composition and pore structure rather than surface area alone. Elemental and morphological analyses suggested that differences in metal-associated components and pore structure may contribute to the higher sorption capacity observed in sludge B. However, the specific sorption mechanisms could not be directly confirmed by the present analyses. Comparison with previous studies confirmed that the measured K_d values fall within reported ranges but are generally higher for sulfonamides, suggesting enhanced sorption capacity of the investigated sludge matrices. Application of an equilibrium-based model demonstrated that sorption alone can account for approximately 20–70% of antibiotic removal under typical activated sludge conditions, depending on compound affinity. These findings highlight the importance of sludge-specific properties in controlling antibiotic partitioning and demonstrate that incorporating such characteristics into predictive models can improve the accuracy of environmental fate assessments in wastewater treatment systems. 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

A one-pot strategy was developed for preparing a chitosan/Mg–Fe layered double hydroxide (LDH) composite by alkaline coprecipitation from an acidic chitosan solution containing Mg(II) and Fe(III) precursors, avoiding separate LDH synthesis and subsequent incorporation into chitosan. X-ray diffraction confirmed LDH formation within the chitosan matrix, and ICP analysis indicated an LDH-equivalent content of approximately 4.1 wt.% on an anhydrous basis. The composite exhibited enhanced chromate adsorption compared with both starting components. The experimental plateau adsorption capacity reached 137.4 mg/g, exceeding those of chitosan (92.2 mg/g) and Mg–Fe LDH (53.5 mg/g). Nonlinear isotherm fitting showed that Mg–Fe LDH was better described by the Freundlich model, whereas chitosan and the composite were better described by the Langmuir model. The kinetic behavior followed the pseudo-second-order equation, while Weber–Morris analysis indicated multistep uptake involving surface interaction and diffusion-related processes. In simulated groundwater containing chloride, bicarbonate, and sulfate, the composite removed 82% of Cr(VI) at 1.0 g/L. It also retained complete chromate uptake over five sorption/desorption cycles, although desorption efficiency decreased from 97.3% to 90.3%. A limitation of this study is that performance was evaluated mainly in batch systems and simplified simulated groundwater; validation with real contaminated waters and dynamic flow conditions is still required. Full article

Sustainable southern highbush blueberry production in Florida is increasingly constrained by freshwater competition, variable rainfall, and the chemical vulnerability of coarse-textured and organic-based production media. Reclaimed water irrigation and biochar amendment are promising strategies for improving water use efficiency and root zone function, but their combined implications for blueberry systems remain insufficiently understood. This review synthesizes the current knowledge on blueberry production requirements, the regulatory and operational context of reclaimed water use, and the physical and chemical roles of biochar in sandy and pine bark-based substrates relevant to horticulture in Florida. Particular emphasis is placed on mechanistic links among reclaimed water chemistry, substrate properties, and root zone processes that govern salinity, pH drift, nutrient retention, and solute leaching. The literature indicates that reclaimed water can improve irrigation reliability and provide supplemental nutrients, but may also introduce sodium, chloride, boron, and other constituents, as well as alkalinity, which alter substrate chemistry and increase the risk of salinity stress and nutrient imbalance. Biochar may enhance water retention, cation exchange, and sorption capacity, but its effects are strongly dependent on feedstock, production conditions, aging, application rate, and substrate context. Overall, successfully integrating reclaimed water and biochar into blueberry systems requires substrate-specific and constituent-resolved evaluation under production conditions relevant in Florida. Full article

Layered double hydroxides (LDHs) are promising anion sorbents, but conventional Mg–Fe LDH synthesis requires prolonged aging. The effects of ultrasound application stage on Mg–Fe LDH microstructure and chromate uptake remain insufficiently clarified. This study compared ultrasonic treatment during and after coprecipitation and related XRD-derived microstructural descriptors to Cr(VI) sorption. Mg–Fe LDHs were synthesized using 28 or 40 kHz ultrasound during or after coprecipitation and 1.7 MHz ultrasound after coprecipitation; 24 h thermal aging was used as a reference. The products were characterized by ICP-MS, FTIR, TGA/DSC, SEM, and XRD and tested for chromate adsorption, kinetics, recyclability, multicomponent-solution performance, and soil Cr(VI) immobilization. Fifteen minutes of ultrasonication yielded Mg/Fe ≈ 2 LDHs and shortened synthesis compared with 24 h aging. Ultrasound during coprecipitation at 28 kHz gave the best sorbent, increasing experimental adsorption capacity to 80.35 mg/g versus 53.70 mg/g for the reference LDH. Sorption followed pseudo-second-order kinetics and was best described by the Freundlich model. In a multicomponent solution, this sample removed 68% Cr(VI) at 1.0 g/L and reduced water-soluble Cr(VI) in soil from 14.31 to 0.26 mg. Ultrasound application during coprecipitation improves Mg–Fe LDH structure-related characteristics and chromate sorption. Full article

This review analyzes the advances over a five-year period in the development of polymeric sorbents for the purification of aqueous media from key classes of pollutants: hydrocarbons (crude oil, diesel fuel), organic dyes, pharmaceuticals (antibiotics), pesticides, herbicides, volatile organic compounds, and polycyclic aromatic hydrocarbons. Attention is paid to the analysis of structure-property-performance relationships, with an emphasis on comparing materials derived from renewable natural feedstocks (such as cellulose, chitosan, terpenes, vegetable oils, and aloe vera) with synthetic polymers. The analysis reveals that biopolymer-based sorbents exhibit comparable or superior sorption capacities combined with environmental safety, biodegradability, and low cost. The key sorption mechanisms include physical adsorption, hydrophobic interactions, and electrostatic interactions. Despite persisting challenges related to scalability, stability in real-world environments, and the need for efficient regeneration protocols, a convergent approach that combines the advantages of modified natural polymers and functional synthetic components appears to be the most promising strategy for developing cost-effective and sustainable technologies for the restoration of water quality. Full article

Radionuclide contamination of surface water bodies poses a significant environmental challenge, particularly for low-productivity dystrophic systems where natural self-purification capacity is limited. This study aimed to assess the potential of phytoplankton and bottom sediments as biogeochemical barriers for radionuclides. Laboratory modeling of ⁹⁰Sr, ²³³U, ²³⁹Pu, and ²⁴¹Am accumulation was conducted using samples of Lake Dryazlo (Tver Oblast) water and bottom sediments as a representative dystrophic model system. Sorption onto phytoplankton biomass over a single growing season was estimated at 1.89 × 10⁴, 5.41 × 10⁴, 6.64 × 10⁴, and 4.04 × 10⁴ Bq g⁻¹ dry biomass for ⁹⁰Sr, ²³³U, ²³⁹Pu, and ²⁴¹Am, respectively. Actinide immobilization in bottom sediments depended on mineral composition and microbial community activity. Ammophos addition increased radionuclide removal from the liquid phase by 2–5-fold through enhanced phytoplankton productivity, and promoted actinide fixation via phosphate mineral phase formation and stimulation of anaerobic sulfur- and iron-cycling bacteria. These results demonstrate a viable biogeochemical barrier approach applicable to the decommissioning of radioactive waste storage ponds and remediation of radionuclide-contaminated water bodies. Full article

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

Magnetic nanocomposite sorbents are increasingly explored for the remediation of metal-contaminated waters; however, high abiotic removal efficiency may not always translate into biological safety. The present study evaluated the single and combined effects of dissolved cobalt (II) ions and magnetite–chitosan nanocomposites (MCN) in zebrafish (Danio rerio) embryos and larvae. MCN (30 wt.% Fe₃O₄) were synthesized via co-precipitation and crosslinking and physiochemically characterized. Adsorption experiments conducted in fish incubation medium demonstrated the efficacy of divalent Co removal and were well described by the Langmuir isotherm model, with a maximum experimental capacity of 20.08 mg g⁻¹. The biological endpoints encompassed survival, hatching, heart rate, locomotor behavior, and oxidative stress biomarkers in early-stage zebrafish. The presence of cobalt (II) was found to result in a reduced hatching success rate, the induction of persistent bradycardia, and the occurrence of oxidative stress, as evidenced by a decline in SOD activity and an increase in H₂O₂ and MDA levels. The study found that MCN alone did not lead to mortality or increase peroxide levels or lipid peroxidation, although a modest decrease in SOD activity was observed. In contrast, combined exposure to cobalt and MCN resulted in significant delayed mortality (>85% at 96 h) and early neuromotor impairment. These findings indicate that high abiotic sorption efficiency alone does not guarantee reduced biological toxicity when nanomaterial–metal interactions occur. Consequently, safety assessments of remediation nanomaterials should explicitly consider nanomaterial–metal interactions and developmental stage-specific biological responses. Full article

Ion-imprinting technology based on biosorbents via sorption demonstrates potential for the selective removal of metal ions from water and wastewater. This offers both high sorption capacity and selectivity for specific metals. Current research trends are toward the development of sorbents with minimal environmental impact. Among the most rapidly evolving classes of sorbents are those derived from biopolymers, such as chitosan—a natural derivative of chitin that can be readily functionalized. Due to the growing interest in this topic, it is necessary to summarize the current knowledge. In this article, we provide a comprehensive overview of the latest advances in ion-imprinted chitosan-based materials designed for the purification of metal-contaminated aqueous systems. We conduct a bibliographic analysis and describe a variety of chitosan-based materials exhibiting selectivity toward heavy metals, including chromium Cr(III/VI), cobalt Co(II), nickel Ni(II), copper Cu(II), zinc Zn(II), arsenic As(III/V), cadmium Cd(II), mercury Hg(II), and lead Pb(II). Finally, we discuss future prospects and highlight current research gaps, aiming to guide further scientific exploration and innovation in this promising field. 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