Search Results (2,038)

Crop diseases cause significant losses in agricultural production; early capture and identification of disease spores enable disease monitoring and prevention. This study experimentally optimized the preparation of Au@Ag NRS (Gold core@Silver shell Nanorods) sol as a Surface-Enhanced Raman Scattering (SERS) enhancement reagent via a modified seed-mediated growth method. Using an existing microfluidic chip developed by the research group, disease spores were separated and enriched, followed by combining Au@Ag NRS with Crop Disease Spores through electrostatic adsorption. Raman spectroscopy was employed to collect SERS fingerprint spectra of Crop Disease Spores. The spectra underwent baseline correction using Adaptive Least Squares (ALS) and standardization via Standard Normal Variate (SNV). Dimensionality reduction preprocessing was performed using Principal Component Analysis (PCA) and Successive Projections Algorithm combined with Competitive Adaptive Reweighted Sampling (SCARS). Classification was then executed using Support Vector Machine (SVM) and Multilayer Perceptron (MLP). The SCARS-MLP model achieved the highest accuracy at 97.92% on the test set, while SCARS-SVM, PCA-SVM, and SCARS-MLP models attained test set accuracy of 95.83%, 95.24%, and 96.55%, respectively. Thus, the proposed Au@Ag NRS-based SERS technology can be applied to detect airborne disease spores, establishing an early and precise method for Crop Disease detection. Full article

Nucleosides are of significant interest to biomedical and pharmaceutical research and have been successfully separated in hydrophilic interaction liquid chromatography (HILIC). However, there have been few studies focusing on the retention mechanisms, and detailed retention mechanisms are not clearly understood. The quantitative assessment methodology based on the linear relationship between the observed retention factors and the phase ratio has been shown to be a new tool to investigate the retention mechanisms of polar compounds in HILIC. This study evaluated the retention mechanisms of 16 nucleosides on a bare silica column. The retention contributions by partitioning, adsorption, and electrostatic attractions are quantitatively determined, and the main retention mechanism can be unambiguously identified for each nucleoside. The study results indicate that the main retention mechanism can shift with the salt concentration in the mobile phase, but partitioning seems to dominate at higher salt concentrations. In addition, the partitioning coefficients are measured using the quantitative assessment methodology and have a relatively strong correlation with the log P values of the nucleosides. Considering large errors in the log P values for these very polar compounds, the partitioning coefficients measured experimentally in the HILIC system may provide a more accurate measure for polarity assessment. Full article

A versatile, clear, and accurate method for determining the steady states of multi-component diffusion through composite membranes is presented in this study. This method can be used for simulating and designing membranes with any support orientation with respect to the zeolite film. In the mathematical model of the membrane, it was assumed that mass transport in the zeolite layer occurs by surface diffusion in accordance with the generalized Maxwell–Stefan model. Diffusion in the macroporous support was described by the dusty gas model (DGM). An alternative model of diffusion in the zeolite was proposed to the universally accepted model, which uses a matrix of thermodynamic factors G. Thus, the difficulty of analytically determining this matrix for more complex adsorption equilibria was eliminated. This article is dedicated to methodological and cognitive aspects. The practical features of the method are illustrated using two gas mixtures as examples, namely {H₂, CO₂} and {H₂, n-C₄H₁₀}. The roles of zeolite and support in the separation of these mixtures are discussed. It was demonstrated under what circumstances the presence of the support can be neglected in the steady-state analysis of the membrane. The effect of the alternative application of the dusty gas model or viscous flow only in the microporous support was discussed. Full article

Membranes were assessed on a bench scale for their performance in methylene blue dye separation. The sawdust, along with Brazilian clay and kaolin, were mixed and compacted by uniaxial pressing and sintered at 650 °C. The membranes were characterized by several techniques, including X-ray diffraction, scanning electron microscopy, porosity, mechanical strength, water uptake, and membrane hydrodynamic permeability. The results demonstrated that the incorporation of sawdust not only altered the pore morphology but also significantly improved water permeation and dye removal efficiency. The ceramic membrane had an average pore diameter of 0.346–0.622 µm and porosities ranging from 40.85 to 42.96%. The membranes were applied to the microfiltration of synthetic effluent containing methylene blue (MB) and, additionally, subjected to investigation of their adsorptive capacity. All membrane variants showed high hydrophilicity (contact angles < 60°) and achieved MB rejection efficiencies higher than 96%, demonstrating their efficiency in treating dye-contaminated effluents. Batch adsorption using ceramic membranes (M0–M3) removed 34.0–41.2% of methylene blue. Adsorption behavior fitted both Langmuir and Freundlich models, indicating mixed mono- and multilayer mechanisms. FTIR confirmed electrostatic interactions, hydrogen bonding, and possible π–π interactions in dye retention. Full article

The application of microsphere molecularly imprinted materials for the targeted extraction and purification of flavonoids derived from agricultural waste has emerged as a prominent area of investigation. An innovative boronate affinity imprinted microsphere (MC-CD@BA-MIP) was successfully synthesized using the Pickering emulsion interfacial assembly strategy for the selective separation of naringin (NRG). The double-bond functionalized covalent organic framework (COF)-based microspheres were synthesized through Schiff–base reaction and secondary interfacial emulsion polymerization. Then, the synthetic mono-(6-mercapto-6-deoxy)-β-cyclodextrin (SH-β-CD) was grafted onto the surface of the microspheres (MC) using click chemistry. The 1-allylpyridine-3-boronic acid (APBA) as a functional monomer was grafted onto the initiator (ABIB) through atom transfer radical polymerization (ATRP). Ultimately, the synthesized boronic acid-imprinted ABIB-BA-MIPs were immobilized onto the COFs microsphere surface through host–guest interactions. As expected, under neutral conditions, the MC-CD@BA-MIPs still exhibited a significant adsorption capacity (38.78 μmol g⁻¹ at 308 K) for NRG. The regenerated MC-CD@BA-MIPs maintained 92.56% of their initial adsorption capacity through six consecutive cycles. Full article

Developing highly permeable and selective membranes for energy-efficient CO₂/CH₄ separation remains challenging. Mixed-matrix membranes (MMMs) integrating polymer matrices with metal–organic frameworks (MOFs) offer significant potential. However, rational filler–matrix matching presents substantial difficulties, constraining separation performance. In this work, defects were engineered within fluorinated MOF ZU-61 through the partial replacement of 4,4′-bipyridine linkers with pyridine modulators, producing high-porosity HP-ZU-61 nanoparticles exhibiting a 267% BET surface area enhancement (992.9 m² g⁻¹) over low-porosity ZU-61 (LP-ZU-61) (372.2 m² g⁻¹). The HP-ZU-61/6FDA-DAM MMMs (30 wt.%) demonstrated homogeneous filler dispersion and pre-served crystallinity, achieving a CO₂ permeability of 1626 barrer and CO₂/CH₄ selectivity (33), surpassing the 2008 Robeson upper bound. Solution-diffusion modeling indicated ligand deficiencies generated accelerated diffusion pathways, while defect-induced unsaturated metal sites functioned as strong CO₂ adsorption centers that maintained solubility selectivity. This study establishes defect engineering in fluorinated MOF-based MMMs as a practical strategy to concurrently overcome the permeability–selectivity trade-off for efficient CO₂ capture. Full article

Flotation separation of fluorite and calcite, by adding AWG (acidified water glass) as inhibitor and NaOL (sodium oleate) as collector, has been investigated by means of micro-flotation tests, flotation solution chemistry, zeta potential measurements, Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS) in this study. The micro-flotation results demonstrate that NaOL exhibits strong collecting power toward both fluorite and calcite, making effective separation of the two minerals unachievable in the absence of depressants. When AWG is applied as a depressant, it shows selective depression toward calcite, while exhibiting little effect on fluorite. Solution chemistry analysis, contact angle measurements, zeta potential measurements, FTIR, and XPS analyses collectively confirm that AWG can adsorb onto the calcite surface, but not onto fluorite. This adsorption prevents NaOL from interacting with the calcite surface. In contrast, the absence of AWG adsorption on fluorite allows NaOL to freely adsorb and thereby collect fluorite particles. Full article

Rivers, vital for life and civilizations, face severe threats from human activities such as hydropower development, with heavy metal pollution emerging as a critical concern due to altered biogeochemical cycles. Understanding how river damming affects heavy metal transport processes and developing targeted remediation strategies are essential for safeguarding the health of river-reservoir ecosystems and enabling the sustainable utilization of hydropower resources. Therefore, this review first summarizes the global hydropower development, details how damming disrupts hydrology, environments, and ecosystems, and analyzes heavy metal distribution and transport in reservoir water, suspended sediments, and riverbed sediments. It reveals that river damming promotes heavy metal adsorption onto suspended particles, deposition in riverbed sediments, and re-release during reservoir regulation, and anthropogenic activities are a primary driver of significant pollution in key reservoirs worldwide. Additionally, we further evaluate in situ (e.g., stabilizing agents, sediment capping, and phytoremediation) and ex situ (e.g., dredging, chemical washing, electrochemical separation, and ultrasonic extraction) remediation techniques, highlighting the challenges of phytoremediation in deep, stratified reservoir environments. Moreover, solidification/stabilization emerges as a promising in situ strategy, emphasizing the need for specific approaches to balance pollution control with hydropower functionality in dammed river systems. Full article

The separation of organic dyes from wastewater (WW) is a major challenge in water pollution control. The present research utilised agricultural residuals from Sapindus mukorossi were utilised to prepare high-performance biochar through carbonization and KOH activation, while its efficiency was evaluated in removing methylene blue (MB). The physicochemical characteristics of the unactivated Sapindus shell biochar (SH0) and activated Sapindus shell biochar (SH2) material were characterised via EA, FTIR, BET, and SEM analyses. The findings indicated that the KOH activated Sapindus shell biochar (SH2) exhibited higher adsorption efficiency in comparison to Sapindus shell biochar (SH0). In particular, the SH2 demonstrated an 11.2-fold higher adsorption capacity for MB (502.11 mg·g⁻¹) compared to SH0, a performance enhancement driven by its remarkably porous structure, substantial total pore volume (0.56 cm³·g⁻¹), and high specific surface area (871.04 m²·g⁻¹). A high MB removal efficiency of 98.36% was achieved within 30 min under the following optimal conditions: a KOH/SH0 activation ratio of 2:1, pH 6.5, and a biochar dose of 0.2 g·L⁻¹. The MB adsorptive process was studied by applying the Langmuir isotherm and PSO kinetic models, suggesting physical and chemical interaction mechanisms between MB dyes and SH2. These findings provide a feasible strategy for the application of Sapindus shells and offer technical support for effectively removing dyes from wastewater by KOH-modified biochar. Full article

MOF-808 was synthesized using different (perfluoro)carboxylic acid modulators, including acetic acid (AA), butyric acid (BA), trifluoroacetic acid (TFAA) and heptafluorobutyric acid (HFBA). These samples were incorporated into co-polyimide 6FDA-DAM:DABA (6FDD), and the performance of the resulting MMMs was assessed for C₂ and C₃ olefin/paraffin separation. Enhanced permeability was observed for both C₂H₄/C₂H₆ and C₃H₆/C₃H₈ mixtures thanks to the introduced porosity upon filler incorporation in all cases. Due to the large pore size of MOF-808, diffusion-selective permeation through the polymer phase of the MMMs determined the eventual selectivity for C2 gases, leading to separation factors similar to that of the unfilled 6FDD membrane. For C₃H₆/C₃H₈ separation, the incorporation of fluorinated MOFs significantly improved separation performance, unlike their non-fluorinated counterparts. The unfilled 6FDD membrane exhibited a C₃H₆/C₃H₈ separation factor of 7.4 with a C₃H₆ permeability of 22 Barrer, while the incorporation of MOF-808-TFAA and MOF-808-HFBA led to C₃H₆/C₃H₈ separation factors of 13.1 and 13.5 with corresponding improved C₃H₆ permeabilities of 42 Barrer and 33 Barrer, respectively. Considering that these MMMs showed C₃H₆ permeabilities similar to those of MMMs containing their non-fluorinated MOF counterparts that exhibited no enhancement in membrane selectivity, the improved C₃H₆/C₃H₈ separation factor was attributed to the preferential adsorption of C₃H₈ over C3H6 on the fluorinated MOFs, acting as a trap for C₃H₈ and reducing its diffusivity. These results highlight the significance of matching the permeation characteristics of the selected polymer-filler pair on MMM performance for different gas pairs. Full article

The galvanic industry requires considerable amounts of water and produces significant quantities of wastewater. Two types of wastewater are created in the processes of the galvanic application of metal coatings: used galvanic baths and wastewater generated while rinsing coated elements. The composition and amount of wastewater depend on the type of process, the plant’s operational system, and the quantity of water utilised to rinse the coated elements. In this article, the possibilities of using different techniques, such as chemical precipitation, coagulation and flocculation, ion exchange, adsorption, and membrane filtration, to remove heavy metals from galvanic wastewater were analysed and assessed. It was determined that the use of physicochemical methods (i.e., chemical precipitation, coagulation, and flocculation) to remove heavy metals has significant disadvantages, including operational costs connected with the purchase of chemical reagents and the emergence of metal complexes requiring management/utilisation. On the other hand, the processes of ion exchange and adsorption can be used only for wastewater characterised by a low heavy metal concentration, with organic matter preliminarily removed. In addition, waste polluted with heavy metals in the form of used regenerative baths and used sorbents is generated during these processes. In turn, the advanced techniques of membrane filtration allow for the removal of different types of organic pollutants and heavy metals. The processes of membrane wastewater treatment exhibit a range of advantages compared to traditional technologies, including the complete, environmentally friendly removal of permanent organic pollution, easy integration into conventional technologies, a limited amount of residue, a high level of separation, and a shorter process time. The efficiency of membrane wastewater treatment depends on many parameters, including, most of all, the composition, pH, and type of membrane, as well as process conditions. The possibility of using new types of membranes to remove heavy metals from spent galvanic baths was analysed, and the possibility of using the processes in wastewater treatment systems according to the circular economy model was assessed. The assessment of the efficiency of heavy metal removal in hybrid systems combining specific individual processes and the development of state-of-the-art material solutions to realise these processes may be an interesting direction of research in this field. Full article

Food contamination poses a significant global public health challenge, necessitating the accurate detection of hazardous substances within complex food matrices. Magnetic core–shell nanomaterials have emerged as critical materials for trace contaminant analysis due to their efficient magnetic separation capabilities, excellent adsorption performance, and tunable surface functionalities. By encapsulating magnetic cores with functional shells, these nanomaterials combine rapid magnetic responsiveness with advantageous shell properties, including target-specific recognition, enhanced dispersibility, colloidal stability, and high surface area. This enables a comprehensive detection approach encompassing target adsorption, rapid separation, and signal amplification. Magnetic core–shell nanomaterials have been effectively integrated with techniques including magnetic solid-phase extraction (MSPE), fluorescence (FL) assays, and lateral flow immunoassays (LFIAs), demonstrating broad applicability in food safety monitoring and detection. This review outlines synthesis strategies for magnetic core–shell nanomaterials, highlights their applications for food contaminant detection, and discusses future challenges and prospects in the field of food safety analysis. Full article

The presence of impurities Fe and trace radioactive U in rare earth elements (REEs) may lead to a significant decline in the performance of high-purity rare earth products. For deep removal from REEs in a green and efficient way, an amine-functionalized silica-based adsorbent, TNDA/SiO₂-P, was prepared by a simple vacuum impregnation method, which had a high organic loading rate of 31.2 wt.%. The experimental results showed that it exhibited good adsorption selectivity for uranium and iron, with separation factors SF_U/REE = 20147 and SF_Fe/REE = 88128 in 5 M HCl. The adsorption kinetics was fast, with equilibrium obtained in 120 min. The 0.1 M HCl can desorb U and Fe efficiently. The deep removal of U and Fe from REEs including Sc can be achieved through chromatographic column separation with high enrichment. FT-IR, XPS and DFT calculations mutually confirmed that protonated TNDA/SiO₂-P exhibited a selective mechanism for uranium and iron in complex anion species in the hydrochloric acid system. This demonstrates its potential for efficiently removing trace impurities U and Fe from REEs. Full article

Direct air capture (DAC) has recently gained interest as a carbon dioxide removal (CDR) method to reduce atmospheric CO₂. DAC is mainly studied through standalone separation technologies, especially adsorption and absorption. Hybrid DAC, combining separation technologies, is rarely investigated and is the main topic of this work. This study investigates hybrid DAC using adsorption for pre-concentration up to a few percent or tens of percent depending on the case studied and membrane separation to concentrate the CO₂ stream to high purity (>90%). Adsorption regeneration by temperature swing adsorption (TSA) and vacuum thermal swing adsorption (VTSA) are compared, and VTSA regeneration achieved higher pre-concentration outlet CO₂ purity (15–30%) than TSA regeneration (1–10%). Membrane separation is studied depending on inlet CO₂ purity and outlet-required purity (90 or 95%), which influence the energy requirement and cost of capture. For all cases studied, the cost of capture remained high (>1700 €/tCO₂) with a high energy requirement (>2 MWh_e/tCO₂ and >27 GJ/tCO₂). The adsorption pre-concentration step accounted for the majority (>80%) of the energy requirement and cost of capture, and future work should be focused on preferentially improving adsorption step performance. Full article

Elucidating the mechanisms of CO₂ photocatalytic conversion systems is crucial for tackling the challenges of carbon neutrality. In this study, a series of Ag@g-C₃N₄ photocatalysts were constructed with metal particle size modulation as the core strategy to systematically reveal the modulation mechanism of Ag nanoparticles (Ag NPs) size variation on the selectivity of CO₂ photoreduction products. Systematic characterizations revealed that increasing Ag size enhanced visible light absorption, promoted charge separation, and improved CH₄ selectivity. Photocatalytic tests showed Ag_3.0%@CN achieved optimal activity and electron utilization. Energy band analyses indicated that Ag modification preserved favorable conduction band positions while increasing donor capacity. Further density-functional theory (DFT) calculations reveal that Ag NPs size variations significantly affect the adsorption stability and conversion energy barriers of intermediates such as *COOH, CO and CHO, with small-sized Ag₇ NPs favoring the CO pathway, while large-sized Ag NPs stabilize the key intermediates and drive the reaction towards the CH₄ pathway evolution. The experimental and theoretical results corroborate each other and clarify the dominant role of Ag NPs size in regulating the reaction path between CO and CH₄. This study provides mechanistic guidance for the selective regulation of the multi-electron reduction pathway, which is of great significance for the construction of efficient and highly selective CO₂ photocatalytic systems. Full article