Search Results (676)

Membrane separation is an efficient approach for volatile organic compound (VOC) recovery from industrial off-gases due to its low energy consumption, compact design, and operational simplicity. Membrane-based VOC recovery critically depends on the membrane material, which must exhibit high VOC permeability and selectivity under mixed-gas conditions. In this study, novel highly selective membranes for VOC removal based on polydecylmethylsiloxane (PAMS-10) were synthesized using both polydimethylsiloxane and various α,ω-dienes as cross-linkers: 1,7-octadiene (OD), 1,9-decadiene (DD), and 1,11-dodecadiene (DdD). The influence of cross-linker concentration and length on mechanical, structural, sorption, and transport properties was examined extensively. The combination of three independent experimental methods (time-lag, vapor permeation, and in situ spectroscopic ellipsometry) revealed that increasing α,ω-diene concentration and decreasing its length led to a reduction in the diffusivity and permeability of permanent gases, gaseous hydrocarbons, and VOC vapors. For VOC/N₂ separation, the slightly cross-linked OD-1 membrane and the DdD-5 membrane, cross-linked with long 1,11-dodecadiene, demonstrated outstanding mixed-gas selectivities of 950/921/314/840 and 940/1084/233/1106 for toluene/n-octane/i-octane/n-butyl acetate, respectively. Notably, the DD-5 membrane, cross-linked with 1,9-decadiene, matching the length of the PAMS-10 side chain substituent, exhibited the best mechanical properties and mixed-gas selectivity comparable to the ideal selectivity, a unique behavior attributed to optimal supramolecular organization. Full article

TiVNbZrCr high-entropy intermetallic alloy was investigated as a deuterium storage material using gravimetric sorption measurements, thermogravimetric analysis, and temperature-resolved synchrotron X-ray diffraction during deuterium desorption. The as-prepared alloy had an experimentally determined composition of Ti₁₇V₁₉Zr₁₉Nb₂₂Cr₂₃ and a density of 6.59 g·cm⁻³. Empirical alloy-design parameters indicate that the alloy is not a single-phase bcc solid solution, but rather a compositionally complex intermetallic alloy. The calculated hydrogen-affinity descriptors suggest a strong thermodynamic driving force for deuteride formation. Under 5 MPa D₂, the alloy absorbed 3.28 wt.% D, corresponding to D/M = 1.1. After ex situ deuteration, additional diffraction reflections were indexed using tetragonal deuteride reference structures corresponding to ZrV₂D_2.35 and TiD₂, while the Cr-rich bcc phase remained comparatively stable. Thermal desorption released 2.28 wt.% D up to 600 °C in three partially overlapping steps. These results demonstrate that deuterium storage in TiVNbZrCr is governed by phase-selective deuteride formation and decomposition rather than by homogeneous bcc lattice expansion. 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

The selective hydrogenation of p-chloronitrobenzene (p-CNB) to p-chloroaniline (p-CAN) is of great importance for the production of dyes, pesticides, and pharmaceuticals, but it is often plagued by the undesired hydrodechlorination side reaction. In this work, we report a PtNi bimetallic catalyst supported on nano-sized LTL zeolite (PtNi/Nano-HL) for the selective hydrogenation of p-chloronitrobenzene under mild conditions. The catalyst was systematically characterized by X-ray diffraction (XRD), nitrogen sorption (N₂ sorption), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and ammonia temperature-programmed desorption (NH₃-TPD). The results reveal abundant oxygen vacancies (RIR = 0.73) and an optimized distribution of medium–strong acid sites on the catalyst surface, as well as electronic interaction between Pt and Ni, which collectively enhance the catalytic performance. Remarkably, the PtNi/Nano-HL catalyst achieves 100% conversion and over 99% selectivity for p-chloroaniline under ambient conditions (30 °C, 0.1 MPa H₂) using ethanol as a solvent. Even after 24 recycling runs, it retains 100% conversion and >93% selectivity, demonstrating excellent stability. Moreover, the catalyst requires an extremely low Pt loading (only 0.11 wt%) and exhibits good substrate universality for various substituted nitroarenes. This work provides a promising strategy for designing high-performance bimetallic catalysts on nano-zeolite supports for the selective hydrogenation of halonitrobenzenes. Full article

This review presents a process-based decision-making framework for chlorinated vapor intrusion (CVI) mitigation. CVI mitigation refers to the set of engineered strategies aimed at interrupting, attenuating or transforming vapor fluxes before they reach indoor environments. Existing literature and technical guidelines typically classify mitigation strategies according to technological configuration (active versus passive), rather than physical and chemical processes governing vapor transport and attenuation, which may lead to suboptimal design choices and reduced system resilience. To address this limitation, this framework proposes a process-based classification of CVI mitigation strategies based on the dominant mechanisms controlling vapor migration in subsurface. Five mechanistic categories are identified: driving-force control through pressure manipulation, dilution via air exchange, diffusive flux control through physical barriers, density-driven attenuation in permeable sub-slab layers, and in situ transformation based on sorption or degradation. By explicitly linking mitigation technologies to transport and transformation processes, the proposed framework provides a structured basis for mechanism-oriented selection, integrating performance, longevity, climate resilience, and lifecycle energy demand. In addition to established mitigation approaches, such as sub-slab depressurization, this work highlights emerging passive strategies, including high permeable granular layers and horizontal reactive or adsorbing barriers, as potential low-energy alternatives for durable management. Overall, the proposed framework supports site-specific, sustainability-oriented decision-making on CVI mitigation. Full article

Industrial processes consume large amounts of thermal energy, while many recoverable heat streams remain unused because heat sources and sinks differ in time, temperature level, power demand, and operating schedule. Thermal energy storage (TES) can decouple heat supply from heat demand and support waste heat recovery, peak-load reduction, process heat electrification, and flexible operation of continuous, batch, and intermittent processes. This narrative review assesses industrial TES from a process integration perspective rather than from a storage-material perspective alone. Sensible, latent, thermochemical, sorption-based, hybrid, and steam-based storage systems are compared with respect to delivery temperature, storage duration, charging and discharging power, response time, heat losses, reliability, integration complexity, and techno-economic feasibility. Sector-specific opportunities are discussed for the iron and steel, cement, ceramics, chemical and petrochemical, pulp and paper, and food and beverage industries. The review shows that deployment is constrained less by the availability of storage concepts than by heat exchanger limitations, inconsistent Key Performance Indicator (KPI) definitions, unclear system boundaries, scarce long-term operating data, and insufficient coupling with pinch analysis, heat exchanger network design, control, and safety requirements. A practical technology-selection workflow and a research roadmap are proposed for scalable, reliable, and economically viable industrial TES deployment. Full article

Magnesium-based hydrides remain among the most intensively studied solid-state hydrogen storage materials because they combine high theoretical hydrogen capacity, elemental abundance, and relatively low cost. Yet their practical behavior often varies far more strongly than nominal composition alone would suggest. Materials described under similar chemical labels may show markedly different activation profiles, sorption kinetics, reversible capacities, and cycling responses, even when they appear compositionally comparable. This Perspective argues that such discrepancies are best understood by recognizing that Mg-based hydrogen storage materials are not fully defined by composition, catalyst identity, and equilibrium thermodynamics alone. Instead, they react from historically written states produced by synthesis, activation, and cycling. These histories generate hidden state variables, including defects, residual strain, metastable structural motifs, interfacial topology, and catalyst transformation states, that reshape the operative hydrogen sorption pathway. The discussion therefore moves from a conventional composition-centered view toward a pathway-centered interpretation of reactivity. First, it examines how hidden state variables are written into Mg-based materials through processing, activation, and repeated use. It then shows how metastability serves as the structural bridge that allows these variables to persist into the reaction window. On that basis, the article argues that hydrogen sorption in Mg-based hydrides is fundamentally pathway-dependent, with history influencing hydrogen entry, transport-network selection, interfacial route construction, and pathway evolution during cycling. This perspective also provides a more coherent explanation for the long-standing reproducibility problem in the field, which is reinterpreted here as a pathway-mismatch problem arising from comparisons among historically different reactive states. Finally, a metadata-aware, pathway-aware, and boundary-aware design framework is proposed as a more realistic basis for cumulative materials development. From this viewpoint, the future of Mg-based solid-state hydrogen storage depends not only on better compositions, but on better-defined, better-constructed, and better-preserved reactive pathways under clearly specified internal and external constraints. Full article

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

Petroleum hydrocarbon contamination of soils remains a persistent environmental problem in Arctic and sub-Arctic regions, where oil extraction, pipeline transportation, fuel storage, industrial legacy sites, and diesel-dependent infrastructure coexist with fragile cold-climate ecosystems. Remediation in these regions is constrained by low temperatures, short thaw seasons, permafrost, waterlogged active layers, slow vegetation recovery, limited infrastructure, and high mobilization costs, which limit the direct transferability of conventional temperate-zone technologies. This study presents a structured narrative review of international and Russian evidence on petroleum-contaminated soil management in cold regions, focusing on monitoring as a basis for remediation decision-making. Peer-reviewed studies, technical guidance documents, regulatory frameworks, and regional case studies were analyzed across key domains, including environmental constraints, hydrocarbon behavior, monitoring methodologies, and remediation technologies. Particular attention is given to chemical analysis, hydrocarbon fractionation, bioavailability-oriented methods, ecotoxicological bioassays, and microbial indicators as tools linking contamination assessment with remediation strategy selection. Reliance on total petroleum hydrocarbon (TPH) concentration as a primary endpoint is shown to be insufficient, especially in cold-region soils where strong sorption and limited mass transfer decouple concentration from biological exposure. Multi-endpoint monitoring systems provide a more reliable basis for assessing contaminant risk, treatment effectiveness, and soil recovery. For the Russian Arctic, the integration of national recultivation frameworks with risk-based assessment and ecotoxicological monitoring is identified as a key pathway for improving remediation outcomes. A decision-oriented framework is proposed that links environmental conditions, contaminant properties, and monitoring data to support the selection and optimization of remediation strategies. This study supports a transition from concentration-based cleanup toward risk-informed and ecosystem-oriented management of petroleum-contaminated soils in Arctic and sub-Arctic environments. Full article

In fecal sludges (FSs) from non-sewered sanitation systems, bound moisture constituted 46–67% of total moisture across all sanitation types investigated, yet the energetic basis for its resistance to removal has not previously been characterized. Existing classifications of moisture fractions lack quantitative binding energy data, leaving the thermodynamic limits of solid–liquid separation undefined for FS. This study investigates the distribution and binding energies of bound moisture fractions in FS obtained from ventilated pit latrines, urine-diverting dehydrating toilets, and septic tank systems. Bound moisture fractions were determined using moisture sorption isotherms, low-temperature convective drying, nuclear magnetic resonance, and thermogravimetric–differential scanning calorimetry analyses. Results show that interstitial moisture constituted 37–50% of total moisture, followed by vicinal (6–14%) and intracellular (3–9%) fractions, with net isosteric heat rising sharply below 20–30% moisture content (w.b.). Evaporation enthalpy exceeded that of bulk water at moisture contents below ~30% (w.b.), consistent with EPS-mediated adsorption and capillary confinement contributing to increased energy requirements for moisture removal and indicating a transition from capillary-controlled to structure-influenced retention. These findings provide a thermodynamic basis for interpreting why conventional mechanical dewatering stalls at a residual moisture content that differs systematically between VIP, UDDT, and septic tank sludges. These insights are relevant for improving FS treatment strategies, particularly in selecting appropriate combinations of dewatering, drying, and pre-treatment processes. Full article

Although amorphous calcium phosphate (ACP) has been extensively employed as a biomaterial in dental and orthopedic fields, its exploration for environmental applications—particularly in potentially toxic element remediation—remains notably limited in the scientific literature. This study reports the rational design of a multifunctional adsorbent by integrating sodium citrate-stabilized ACP (Cit-ACP) nanoparticles into calcium-crosslinked sodium alginate (SA) hydrogel beads for selective Cu²⁺ sequestration from aqueous systems. Comprehensive sorption assessments revealed that equilibrium uptake aligned with the Freundlich isotherm (indicating heterogeneous surface interactions), while kinetic profiles adhered to pseudo-second-order behavior, characteristic of chemisorption-driven processes. Under optimized operational parameters (pH 5.0, 45 °C), the Cit-ACP/SA composite attained an exceptional maximum adsorption amount of 307.76 mg/g. Thermodynamic analysis further confirmed the spontaneity (ΔG° < 0) and endothermic nature (ΔH° > 0) of the process. Multi-technique characterization (XPS, FTIR, XRD, pH trajectory) elucidated a dual-mode adsorption mechanism: (i) ion exchange between aqueous Cu²⁺ and structural Ca²⁺ within both the alginate matrix and ACP framework; and (ii) in situ surface precipitation yielding copper-substituted hydroxyapatite. Owing to its facile aqueous-phase synthesis, superior adsorption performance, biodegradability, macroscopic bead morphology enabling rapid separation, and robust selectivity in complex matrices, the Cit-ACP/SA composite presents a sustainable, scalable, and eco-compatible platform for practical remediation of copper-contaminated wastewater. Full article

Wastewater generated during the processing of roasted coffee, including instant coffee, remains relatively unknown in the literature. However, it is characterized by a high organic load and the presence of caffeine, phenolic compounds, and melanoidins. Its properties pose significant environmental and technological challenges, limiting the effectiveness of conventional treatment methods. The research aimed to evaluate the effectiveness of an integrated, multi-stage wastewater treatment system that reflects the process of roasted coffee extraction. The developed technological sequence included biological treatment, activated carbon sorption, membrane filtration, and disinfection using ozone and UV radiation. The experiments used synthetic wastewater containing an extract of roasted coffee beans to simulate the contaminants typically found in instant coffee production and the cleaning of processing equipment. The integrated treatment system enabled the removal of total organic carbon (82.4–95.4%), ammonium nitrogen (0–77.4%), and phosphates (0–39.9%), and a reduction in turbidity of 96.3–99.8% at pH 4.02–7.25. The results confirm the system’s high efficiency and its potential for treating complex coffee wastewater, while also highlighting the need for further research into the selection of more favorable process parameters. Full article

Damage to urban water supply infrastructure can rapidly compromise access to safe water and force households to rely on alternative sources of uncertain quality. This study presents a case-based assessment of water quality and emergency household-level treatment options in Mykolaiv, Ukraine, following conflict-induced disruption of the centralized water supply system. Water samples collected from selected groundwater and distribution-network points were analyzed for physicochemical, organoleptic, and microbiological indicators, including total dissolved solids, hardness, sulfates, chlorides, iron, permanganate oxidizability, total microbial count, and E. coli. The results showed elevated mineralization, increased sulfate and chloride concentrations, high hardness, organic load indicators, and episodic microbiological contamination in several samples. A low-cost four-stage household treatment procedure combining chemical oxidation, thermal treatment, sorption, and short-term preservation was evaluated as a preliminary emergency approach. The procedure improved odor, taste, hardness, iron content, permanganate oxidizability, and microbiological safety; however, it did not fully reduce total dissolved solids, sulfates, or chlorides to drinking-water standards. Therefore, the treated water should be considered non-potable and suitable mainly for limited domestic and hygienic uses unless additional desalination or blending is applied. The study highlights both the potential and the limitations of simple household-level interventions under emergency water supply disruption and emphasizes the need for decentralized treatment support, monitoring, and long-term infrastructure recovery. Full article

Repurposing mineral processing waste offers both environmental and economic benefits, reducing the disposal burden while enabling mineral resource recovery. A magnetic adsorbent, with an Fe₃O₄ content of 71.0%, collected from waste copper converter slag was utilized to recover gold (Au³⁺) from chloride solution. The adsorbent was separated from the slag samples by crushing, grinding to an average particle size of 30 μm, and magnetic separation. Batch adsorption experiments were performed to evaluate the effects of pH, contact time, chloride concentration, and initial gold concentration on gold uptake amount. The material recovered over 99% of gold from chloride solution under acidic conditions and in the near-neutral pH range. The gold sorption rate was also relatively fast and over 98% recovery was achieved after just 15 min of contact time. Increasing chloride concentration did not influence gold uptake. Parameter studies and spectrometric analyses suggest that chalcocite (Cu₂S) and metallic copper present in magnetite slag reduced the gold chloride complex to metallic gold. These results suggest that converter magnetite slag is a potentially effective sorbent to recover gold from secondary sources due to its selectivity and low cost. Moreover, gold-loaded magnetite slag can be easily separated from the solution by magnetic separation and then recirculated to the smelting stage of copper processing to recover the deposited gold and other precious metals. Overall, this work highlights a pathway to transform waste into opportunity, reinforcing sustainability in mineral processing operations. Full article

The calcination kinetics of limestone and dolomite under conditions relevant to sorption-enhanced gasification (SEG) were investigated: mild temperature (775–850 °C), low CO₂ partial pressure (0.05–0.10 bar), and a steam-rich (H₂O balance) atmosphere. Experiments with two Ca-based sorbents (limestone and dolomite) were conducted in a fluidized bed reactor to assess both initial calcination kinetics and multicycle deactivation during 10 cycles under SEG carbonation conditions at 650 °C. Dolomite exhibited markedly higher calcination rates than limestone, which is consistent with the structural modifications induced by MgCO₃ decomposition and the presence of MgO, resulting in a slightly lower apparent activation energy (115.96 kJ mol⁻¹ for dolomite compared to 120.27 kJ mol⁻¹ for limestone). Both sorbents showed a strong sensitivity to the deviation from the equilibrium CO₂ partial pressure, with reaction orders near 2. The presence of steam was confirmed to have a significant catalytic effect, accelerating the first-cycle calcination rate compared to dry N₂ conditions. Sorbent deactivation caused by sintering was more pronounced at higher temperatures and CO₂ pressures. Dolomite showed significantly less deactivation, compared to limestone, which can be attributed to the increase in structural stability due to the presence of MgO. The kinetics obtained in this work contribute to the design of stable SEG based on dual fluidized bed reactors, particularly to assist in the selection of calcination operating conditions to minimize sorbent deactivation and in the development of stable CO₂-sorbents. Full article