Search Results (6,731)

Microcellular injection-molded polypropylene/oyster shell nano-powder (PP/OSP) composites show potential as adsorbent materials for reducing toxic metal ion contamination in groundwater. This study investigates the material properties of PP/OSP composites and evaluates their Pb(II) adsorption performance in aqueous media. The effects of key operational parameters, including contact time, pH, and initial Pb(II) concentration, were examined to determine the optimal conditions for heavy metal remediation. The composites were characterized using XRD, SEM, FTIR, and TGA to assess their crystalline structure, surface morphology, functional groups, and thermal stability, respectively. Adsorption isotherm analysis indicated that the Pb(II) uptake behavior followed both the Freundlich and Temkin models. Kinetic studies showed that the adsorption process was best described by the pseudo-first-order model. The maximum adsorption capacity for Pb(II) removal was determined to be 13.89 mg/g. Full article

Balancing high fluidity and stability is a critical challenge in deep-shaft cemented paste backfill (CPB) with high-concentration tailings. This study investigates the synergistic regulation mechanism of a combined admixture system comprising hydroxypropyl methylcellulose (HPMC) thickener and polycarboxylate (PCE) or Melamine-Formaldehyde Resin (MFR) superplasticizers on CPB rheology, mechanical strength, and microstructure. Results indicate that HPMC significantly enhanced anti-segregation performance via intermolecular bridging, substantially increasing yield stress and plastic viscosity. Upon PCE introduction, the steric hindrance provided by its side chains effectively disrupted HPMC-induced flocs and released entrapped water. Consequently, yield stress and plastic viscosity were reduced by up to 22.1% and 64.3%, respectively, with PCE exhibiting markedly superior viscosity-reducing efficiency compared to MFR. Mechanical testing revealed that PCE co-addition did not compromise early-age strength but enhanced 3, 7, and 28-day unconfined compressive strength (UCS) by refining pore structures and promoting the uniform distribution of hydration products. Microstructural analysis unveiled a competitive adsorption mechanism: preferential PCE adsorption dispersed particle agglomerates, while non-adsorbed HPMC formed a viscoelastic network within the pore solution, constructing a stable “dispersion-suspension” microstructure. This work provides a theoretical basis for optimizing high-performance backfill formulations. Full article

A cobalt-containing zeolitic imidazolate framework (ZIF-67) was carbonized by different routes to composite materials (cZIFs) composed of metallic Co, Co₃O₄, and N-doped carbonaceous phase. The effect of the carbonization procedure on the water pollutant removal properties of cZIFs was studied. Higher temperature and prolonged thermal treatment resulted in more uniform particle size distribution (as determined by nanoparticle tracking analysis, NTA) and surface charge lowering (as determined by zeta potential measurements). Surface-governed environmental applications of prepared cZIFs were tested using physical (adsorption) and electrochemical methods for dye degradation. Targeted dyes were methylene blue (MB) and methyl orange (MO), chosen as model compounds to establish the specificity of selected remediation procedures. Electrodegradation was initiated via an intermediate reactive oxygen species formed during oxygen reduction reaction (ORR) on cZIFs serving as electrocatalysts. The adsorption test showed relatively uniform adsorption sites at the surface of cZIFs, reaching a removal of over 70 mg/g for both dyes while governed by pseudo-first-order kinetics favored by higher mesoporosity. In the electro-assisted degradation process, cZIF samples demonstrated impressive efficiency, achieving almost complete degradation of MB and MO within 4.5 h. Detailed analysis of energy consumption in the degradation process enabled the calculation of the current conversion efficiency index and the amount of charge associated with O₂^•−/^•OH generation, normalized by the quantity of removed dye, for tested materials. Here, the proposed method will assist similar research studies on the removal of organic water pollutants to discriminate among electrode materials and procedures based on energy efficiency. Full article

Zeolites and molecular sieves have demonstrated remarkable potential in adsorption, ion exchange, and separation processes since their industrial revolution in the 1950s. Zeolites and molecular sieves are materials of choice in separation applications because of their well-defined microporous architecture, remarkable shape-selectiveness, and tunable characteristics. The adsorption process can be evaluated using an isotherm to determine the feasibility of gas mixture separation for practical applications. We will also discuss the basic structure of zeolites and molecular sieves based on different metals, along with their distinctive properties in detail. The purpose of this review is to contextualize the importance of zeolites and molecular sieves in adsorption and separation applications. The review has been divided into groups based on how zeolites as well as molecular sieves are established in the adsorption and separation processes. The fundamental adsorption characteristics, structures, and various separation methods that make zeolites appealing for different uses are covered. By incorporating knowledge of adsorption mechanisms, isotherms, and material changes, this review discusses the most recent developments. To augment zeolite-based materials for certain pollutant removal applications, it offers a strategic framework for future study. In this review, we will comprehensively discuss a range of separation and adsorption applications, including wastewater purification, CO₂ capture from flue gases, and hydrogen storage. Furthermore, the review will explore emerging prospects of zeolites and molecular sieves in innovative fields such as energy storage, oil refining, and environmental remediation. Emphasis will be placed on understanding how their tunable pore structures, surface chemistry, and metal incorporation can enhance performance and broaden their applicability in sustainable and clean energy systems. Full article

China has abundant deep coalbed methane (CBM) resources; however, high temperature, stress, and reservoir pressure complicate the gas adsorption–desorption–diffusion–seepage processes, severely restricting the development of deep CBM. Through experimental research on adsorption, desorption, diffusion, and seepage behaviors of various coal samples, the control mechanisms of deep coal reservoir properties on CBM production in the Linxing–Shenfu region have been revealed. The results indicate that CBM adsorption and desorption characteristics are jointly controlled by coal rank, ash yield, temperature. and pressure. Among the above conditions, coal rank and pressure exhibit positive effects, while ash yield and temperature show inhibitory effects. Analysis of desorption efficiency based on the Langmuir model further identifies sensitive desorption and rapid desorption stages as key phases for enhancing productivity. Moreover, the gas diffusion mechanism is dynamically evolving, with Knudsen diffusion and Fick diffusion being the main modes during high ground pressure stages, gradually transitioning to the coexistence of Knudsen, transition, and Fick diffusions as pressure decreases. Concurrently, gas–water seepage experiments demonstrate that increasing temperature will reduce the irreducible water saturation and enhance the relative permeability of the gas. Since irreducible water saturation is negatively correlated with relative permeability of gas, the relative permeability of the gas phase, cross-point saturation, and the range of the two-phase co-seepage zone all significantly increases with the increase in temperature. The findings systematically elucidate the regulatory mechanisms of deep coal reservoir properties in the process of “adsorption–desorption–diffusion–seepage,” providing critical theoretical support for optimizing development strategies and enhancing the efficiency of deep CBM development. Full article

The influence of 5-Methyl-1H-benzotriazole (MHBTZ) on the corrosion of pure iron (Fe) and aluminum (Al) in 1 M HCl was investigated in this study. The experimental and theoretical aspects of MHBTZ adsorption onto pure iron (Fe) and aluminum metal (Al) surfaces, as well as the stability of adsorbed layers based on the metal type, were also studied. Different electrochemical measurements were performed to explore the corrosion rates and inhibition efficiencies on the Fe and Al surfaces at 298 K. Optical profilometry was used to obtain the 3D surface topography of Fe and Al metals after immersion with and without the MHBTZ molecule. The results showed that MHBTZ exhibited excellent inhibition properties for both metals. Electrochemical impedance spectroscopy (EIS) achieved inhibition efficiencies of 98.1% and 98.5% for Fe and Al, respectively, at a concentration of 2500 ppm. Potentiodynamic polarization (PDP) indicated that MHBTZ acted as a mixed-type inhibitor. Density functional theory (DFT) analysis and molecular dynamics (MD) simulations were used to explore the relationship between the molecular structure of MHBTZ and its inhibition efficiency at the atomic level. Full article

The objective of this study was to valorise eggshell waste (ESW) by investigating its biosorption properties and evaluating its efficiency as a sustainable biosorbent for the removal of the synthetic dye Congo Red (CR) from model CR solutions and synthetic wastewater with the addition of CR. Batch biosorption experiments were conducted to investigate the influence of several factors on the biosorption process, including ESW concentration (1–15 g L⁻¹), contact time (1–360 min), temperature (15, 25, 35, 45 °C) and initial CR concentration (10–100 mg L⁻¹). Desorption experiments were performed using ultrapure water, 0.1 M NaCl, 50% ethanol, 0.1 M HCl, or 0.1 M NaOH as solvents. A higher ESW concentration improved CR removal, but the amount of CR adsorbed on ESW decreased. The dye uptake by ESW was increased with prolonged contact time and temperature increase. When the effect of CR initial concentration was investigated, the results indicated that the process is concentration-dependent and that overall, CR uptake by ESW was higher in synthetic wastewater than in the model dye solution. The biosorption process was better described by the Langmuir isotherm model than by the Freundlich model, indicating monolayer adsorption. Kinetic analysis showed that the pseudo-second-order model provided a better fit than the pseudo-first-order model. Desorption of CR from ESW under the applied experimental conditions was generally low (0.67–27.13%). Full article

The integration of graphene-based materials with metal–organic frameworks (G@MOFs) has emerged as a promising strategy for advanced wastewater treatment owing to their synergistic physicochemical properties. This review systematically compiles and critically analyzes recent advances in the synthesis, structural characterization, and application of G@MOFs for the removal of organic and inorganic micropollutants. Special emphasis is placed on how the unique combination of high surface area, tunable pore structures, and abundant active sites in G@MOFs enhances adsorption, photodegradation, and catalytic degradation mechanisms. Compared to conventional adsorbents and standalone MOFs, G@MOFs exhibit superior removal capacities, stability, and reusability. This paper also identifies key challenges in large-scale applications, regeneration, and potential environmental risks, providing a future outlook on optimizing synthesis routes and tailoring functional composites for sustainable water treatment technologies. The novelty of this review lies in providing the first dedicated, systematic evaluation of G@MOFs for wastewater micropollutant removal, integrating synthesis strategies, performance benchmarking, techno-economic aspects, environmental safety, and future application prospects into a unified framework. Full article

This study aimed to synthesize a magnetic biochar@ZIF-8 composite derived from almond shell biomass for the adsorption of fluoroquinolones (FQs) from aqueous media. The biochar was prepared under different pyrolysis conditions using a central composite design (CCD) based on temperature and residence time, with biochar yield (%) and ofloxacin adsorption capacity selected as the response variables. Subsequently, the composite was obtained by combining KOH-activated biochar with ZIF-8 and magnetic particles, producing a hierarchically porous material with enhanced surface area and functional groups favorable for adsorption. The physicochemical and morphological properties of the composite were characterized by SEM–EDS, FTIR, BET, TGA, and XRD analyses, confirming the successful incorporation of ZIF-8 and magnetic phases onto the biochar surface. The adsorption performance was systematically evaluated by studying the effects of pH and contact time. The kinetic data fitted well to the pseudo-second-order model, suggesting that chemisorption predominates through π–π stacking, hydrogen bonding, and coordination interactions between FQ molecules and the active sites of the composite. Furthermore, the material exhibited high reusability, maintaining over 84% of its adsorption capacity after four cycles, with efficient magnetic recovery without the need for filtration or centrifugation. Overall, the magnetic biochar@ZIF-8 composite demonstrates a sustainable, cost-effective, and magnetically separable adsorbent for water remediation, transforming almond shell waste into a high-value material within the framework of circular economy principles. Full article

This study presents a novel approach for synthesizing porous silica materials using various biomass-derived carboxylic acids as non-surfactant, eco-friendly porogens. Different carboxylic acids were selected, and their influence on the properties of the final materials was systematically investigated. The silica synthesis was performed using only the intrinsic acidity of carboxylic acids without pre-hydrolysis of the silica precursor - tetraethyl orthosilicate (TEOS). Citric and tartaric acids had a favorable effect on the formation of mesoporous silica, whereas the oxalic, ascorbic, maleic, and mandelic acids led to the formation of microporous silica. The optimal synthesis compositions and parameters were thoroughly investigated. A mesoporous silica with a uniform pore size was prepared using tartaric acid, and the pore size was controlled by the drying temperature. Template removal via water extraction yielded silica materials with superior textural properties compared to conventional high-temperature calcination, while allowing the recovery and reuse of organic acids. Our results confirm that using carboxylic acids can be efficiently and economically applied for the controlled synthesis of mesoporous silica suitable for different applications, such as adsorption, drug delivery, and catalysis. Full article

Polyphenols like dihydroquercetin, rutin, and rifampicin show promise for Alzheimer’s disease (AD) therapy due to their ability to inhibit amyloid-β (Aβ) aggregation and reduce reactive oxygen species (ROS), garnering significant recent interest. However, their efficacy is substantially diminished because excess metal ions present in amyloid plaques can chelate these compounds. Therefore, reshaping the metal microenvironment in the patient’s brain is particularly important for the therapeutic effect of AD. To address the above issues, we have constructed a composite system formed by NH₂-MIL-101(Fe) (MOF), dihydroquercetin (DHQ), and D-penicillamine (D-pen). Due to the lack of π-π interaction and the low adsorption energy between D-pen/MOF, the release order and speed of D-pen was much faster than DHQ, thus achieving metal microenvironment regulation and ensuring the therapeutic effect of DHQ. In a 5 × FAD transgenic mouse model, DD@MOF treated and improved spatial learning and memory deficits. Therefore, the DD@MOF based on polyphenolic compounds provides a potential research direction for intervention in Alzheimer’s disease through chelating copper ions and antioxidant properties. Full article

The continuous tightening of emission regulations and the escalating costs of palladium (Pd) and rhodium (Rh) have renewed interest in platinum (Pt)-based three-way catalysts (TWCs) as cost-effective alternatives for gasoline aftertreatment. However, despite extensive studies on Pt/CeO₂ and Pt/Ba-based formulations, the cooperative roles of Ba and Ce and, in particular, the fundamental influence of the Ba/Ce ratio on oxygen mobility, NO_x storage behavior, and Pt–support interactions remain poorly understood. In this work, we address this gap by systematically tuning the Ba/Ce molar ratio in a series of Pt–Ba–Ce/Al₂O₃ catalysts prepared from Ba(CH₃COO)₂ and CeO₂ precursors, and evaluating their structure–function relationships in both fresh and hydrothermally aged states. Through comprehensive characterization (N₂ physisorption, XRD, XPS, H₂-TPR, NO_x-TPD, SEM, CO pulse adsorption, and dynamic light-off testing), we establish previously unrecognized correlations between Ba/Ce ratio–dependent structural evolution and TWC performance. The results reveal that the Ba/Ce ratio exerts a decisive control over catalyst textural properties, Pt dispersion, and interfacial Pt–CeO₂ oxygen species. Low Ba/Ce ratios uniquely promote Pt–Ce interfacial oxygen and O₂ spillover—providing a new mechanistic basis for enhanced low-temperature oxidation and reduction reactions—while higher Ba loading selectively drives BaCO₃ formation and boosts NO_x storage capacity. A clear volcano-type dependence of NO_x storage on the Ba/Ce ratio is demonstrated for the first time. Hydrothermal aging at 850 °C induces PtO_x decomposition, BaCO₃–Al₂O₃ solid-state reactions forming inactive BaAl₂O₄, and Pt sintering, collectively suppressing Pt–Ce interactions and reducing TWC activity. Importantly, an optimized Ba/Ce ratio is shown to mitigate these degradation pathways, offering a new design principle for thermally durable Pt-based TWCs. Overall, this study provides new mechanistic insight into Ba–Ce cooperative effects, establishes the Ba/Ce ratio as a critical and previously overlooked parameter governing Pt–support interactions and NO_x storage, and presents a rational strategy for designing cost-effective, hydrothermally robust Pt-based alternatives to Pd/Rh commercial TWCs. Full article

In the context of global energy demands, the efficient demulsification of highly stable heavy crude oil emulsions remains a critical challenge. This study systematically investigated the demulsification mechanisms of two demulsifiers (P1# and P2#) through multi-dimensional characterisation and performance evaluation. The results indicated that asphaltenes and resins can strengthen the oil–water interfacial film and stabilise the emulsion due to their unique structural properties. FTIR and ¹HNMR analyses showed that both demulsifiers contained polar groups and alkyl chains; however, P1# exhibited higher viscosity and lower surface tension, which favored its rapid adsorption at the interface. Demulsification tests at 60 °C demonstrated that P1# achieved superior efficiency (92.44% demulsification efficiency (DE) in 120 min versus 82.31% for P2#), attributable to its enhanced ability to displace asphaltene/resin at the oil-water interface. Turbiscan stability analysis and microscopic observations confirmed that P1#-treated emulsions underwent faster droplet coalescence and significant interfacial film disruption. Mechanistic studies indicated that the demulsifiers competitively adsorb at the interface, thereby weakening film cohesion through steric hindrance and charge redistribution. XRD and FTIR analyses suggested that interactions between the demulsifier and the asphaltene/resin increased interlayer spacing and reduced crystallinity. Zeta potential and interfacial tension measurements further highlighted P1#’s ability to neutralize negative charges (from −14.52 mV to +8.3 mV) and reduce the IFT (from 28.5 mN/m to 12.1 mN/m), thereby promoting droplet aggregation. This study helps elucidate the mechanism of emulsion phase transition induced by demulsifiers and provides theoretical support for improving the demulsification efficiency of crude oil emulsions. Full article

The contamination of water bodies by polycyclic aromatic hydrocarbons (PAHs) poses a significant concern for the ecological systems, along with public health. Magnetic adsorption stands out as a green and practical solution for treating polluted water. To make the process more efficient and economical, it is important to create materials that not only absorb contaminants effectively but also allow for easy recovery and reuse. This study proposes a simple yet effective method for coating Fe₃O₄ nanoparticles with hydroxypropyl-β-cyclodextrin polymer (HP-β-CDCP). The physicochemical properties of the synthesized sorbent were characterized using a transmission electron microscope (TEM), Fourier-transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), and Vibrating Sample Magnetometer (VSM) analysis. The adsorption performance of HP-β-CDCP/Fe₃O₄ nanoparticles was well-described by the pseudo-second-order kinetic model, thermodynamic analysis, and the Freundlich isotherm model, indicating multiple interaction mechanisms with PAHs, such as π–π interactions, hydrogen bonding, and van der Waals forces. Using HP-β-CDCP/Fe₃O₄ nanoparticles as the adsorbent, the purification rates for the fifteen representative PAHs were achieved within the range of 33.9–93.1%, compared to 15.3–64.8% of the unmodified Fe₃O₄ nanoparticles. The adsorption of all studied PAHs onto HP-β-CDCP/Fe₃O₄ nanocomposites was governed by pH, time, and temperature. Equilibrium in the uptake mechanism was obtained within 15 min, with the largest adsorption capacities for PAHs in competitive adsorption mode being 6.46–19.0 mg·g⁻¹ at 20 °C, pH 7.0. This study points to the practical value of incorporating cyclodextrins into tailored polymer frameworks for improving the removal of PAHs from polluted water. Full article

This study presents an approach to synthesizing LTA-type zeolite from spodumene residue generated during a lithium extraction process. A residue was obtained after leaching β-spodumene with 2 mol/L phosphoric acid. After solid–liquid separation, the delithiated residue was first treated with 2 mol/L sodium hydroxide and then subjected to hydrothermal synthesis using sodium aluminate as an additional aluminum source. The resulting material was characterized by XRD, SEM-EDS, XPS, and FTIR, which collectively confirmed the formation of a crystalline material exhibiting the structural features, elemental composition, and morphological characteristics consistent with LTA-type zeolite. Additional analyses, including BET surface area, particle size distribution, and zeta potential measurements, were performed to further evaluate the physicochemical properties of the synthesized zeolite. The spodumene leach residue (SLR)-derived zeolite was further tested for its adsorption performance in heavy metal ions removal from a mixed ion solution containing Pb²⁺, Cu²⁺, Zn²⁺, and Ni²⁺ ions. The zeolite demonstrated a high selectivity for Pb²⁺, followed by moderate uptake of Cu²⁺, while Zn²⁺ and Ni²⁺ adsorption was minimal. These findings demonstrate that spodumene residue, a waste by-product of lithium processing, can be effectively upcycled into LTA zeolite suitable for heavy metal remediation in water treatment applications. Full article