Search Results (313)

Cellulose nanocrystals (CNCs) are renewable and biodegradable nanomaterials that can stabilize Pickering emulsions through steric hindrance and electrostatic repulsion. However, pristine CNCs show limited interfacial anchoring because of their strong hydrophilicity and high surface charge density, making the emulsions susceptible to coalescence, phase separation, and structural instability under environmental stresses. This review summarizes two major strategies for stabilizing and functionally regulating CNC-based Pickering emulsions: chemical modification and synergistic stabilization. Chemical modification regulates CNC surface charge, wettability, interfacial anchoring, and functional group composition through oxidation, amination, esterification, graft copolymerization, desulfation, and etherification, whereas synergistic stabilization constructs composite interfacial films or continuous-phase networks through noncovalent interactions between CNCs and proteins, polysaccharides, cyclodextrins, surfactants, inorganic nanomaterials, or functional molecules. The ability of these emulsion systems to compartmentalize oil-soluble bioactives within structured droplets also provides a basis for improving bioactive stability and release behavior in food-related formulations. These strategies improve emulsion stability and introduce antibacterial, antioxidant, responsive, and controlled-release properties, highlighting the potential of CNC-based Pickering emulsions in active food systems, including food preservation, active packaging, and the stabilization, protection, and release regulation of food bioactives. Remaining challenges in green preparation, structural regulation, release mechanisms, scalable production, and practical evaluation are also discussed. Full article

Environmental pollution by polycyclic aromatic hydrocarbons (PAHs) is a serious environmental problem. One of the effective methods of cleaning the environment from these toxicants is the use of sorbents based on clay minerals. Special organo-mineral, bio-mineral and bio-organo-mineral complexes were obtained. Organo-mineral complexes (organoclays) were synthesized on the basis of Na-bentonite and anionic, amphoteric and nonionic surfactants. Bio-mineral and bio-organo-mineral complexes were produced by inoculating bentonite and organoclays with a consortium of bacteria. The adsorption characteristics of the complexes to benzopyrene and naphthalene were studied. Modification of bentonite with various types of surfactants leads to a significant increase in the percentage adsorption of both benzopyrene and naphthalene, with benzopyrene being more so. All bio-organo-mineral complexes adsorb more benzopyrene than pure bentonite and the bentonite + bacteria complex. In most cases, this pattern is also characteristic of naphthalene adsorption. Organoclay complexes with bacteria adsorb PAHs in greater quantities than organoclays, typically at the average concentrations of benzopyrene and naphthalene used (30–60 μg mL⁻¹) and when modified with individual surfactants. Based on the determination coefficients, the adsorption of benzopyrene and naphthalene by all studied sorbents is best described by the Langmuir equation. The maximum (limiting) adsorption of benzopyrene by all organo-mineral complexes (organoclays) exceeds the maximum adsorption of benzopyrene by bentonite. Modification of bentonite with surfactants may not change, decrease, or increase the maximum adsorption of naphthalene compared to the original bentonite, depending on the surfactant used. Colonization of the organoclay surface by bacteria, with rare exceptions, results in a decrease in the maximum adsorption values of benzopyrene and naphthalene compared to organoclay, or has no effect at all. Full article

Direct utilization of biomass-derived silica in neutral surfactant-templated mesoporous synthesis remains underexplored with respect to mesostructure control and functional integration. High-purity silica extracted from acid-treated rice husk ash (~98.4 wt% SiO₂) was employed as the sole precursor in a fluoride-assisted sol–gel route to synthesize MSU-X frameworks without chemical modification. Systematic parametric variation—pH, Si/surfactant ratio, hydrothermal temperature, and aging duration—establishes quantitative structure–processing correlations. Under optimized conditions (pH 2, Si/Tergitol = 8, 60 °C, 96 h), the resulting material exhibits a wormhole-like mesoarchitecture with a BET surface area of 816 m² g⁻¹, mean pore diameter of ~3.6 nm, and three-dimensionally interconnected channels, confirmed by SAXS, TEM, and N₂ sorption. EDXRF analysis confirms effective impurity removal and high silica incorporation efficiency (~95–96%); thermal stability persists to 700 °C, with incipient crystallization near 800 °C. As a functional demonstration, MSU-X served as an anti-agglomeration scaffold for ZIF-8 crystallization during DDT adsorption. Despite attenuated kinetics relative to pristine ZIF-8—where severe agglomeration occludes active imidazole nodes—the Z8/MSU-X composite achieved near-quantitative DDT removal (74.10 mg g⁻¹). This performance stems from the mesoporous matrix driving size-confined, highly dispersed ZIF-8 growth, thereby maximizing active-site exposure. Operating within a reagent-limited regime rather than a capacity-saturated boundary, this efficient depletion confirms that the scaffold successfully suppresses site loss. Ultimately, these findings validate biogenic silica as a directly integrable precursor for tailored mesostructure assembly, positioning agricultural waste as a high-performance feedstock for hierarchical adsorption architectures. Full article

Raw lacquer, a natural polymer derived from the bast of lacquer trees (Toxicodendron vernicifluum), is renowned as the “King of Coatings” due to its exceptional film-forming properties, abrasion resistance, corrosion resistance, and biocompatibility. However, its inherent limitations—including stringent drying conditions, slow curing rates, deep coloration, and difficult application—have severely restricted its modernization and widespread adoption. This review systematically summarizes recent research advances in the modification and application of raw lacquer, focusing on four major modification strategies: (1) Nanocomposite modification—incorporating functional nanofillers such as Al₂O₃, cellulose nanofibrils (CNF), polydopamine (PDA) melanin-like nanoparticles, and SiO₂ to significantly enhance film hardness, compactness, UV-aging resistance, and drying kinetics. (2) Chemical structure modification—employing molecular design strategies including aminoanthraquinone grafting, tung oil blending, water-based emulsification, and terpene/allyl group functionalization to improve hydrophobicity, flexibility, fast-drying properties, and achieve dual photo/oxygen curing. (3) Biomass synergistic composites—utilizing natural polymers such as chitosan and lignin, along with bio-inspired adhesion mechanisms (e.g., PDA), to confer advanced functionalities including antibacterial and antifouling properties. (4) Curing behavior regulation—precisely controlling drying kinetics through inorganic salt ion microenvironment engineering, nonionic surfactants, and salicylaldehyde Schiff base-based driers. Building upon these foundations, this review further expands on the emerging high-value applications of modified lacquer in preventive conservation of cultural heritage, advanced functional coatings (anti-corrosion, super-hydrophobicity, flame retardancy), biomedical materials (hemostasis, antibacterial activity, drug-controlled release, water treatment adsorption), and intelligent responsive flexible electronics. Finally, addressing challenges including weak fundamental research, bottlenecks in green industrialization, and lack of standardization, future development directions are proposed encompassing interdisciplinary innovation, sustainable modification strategies, integration of multifunctional intelligent systems, and big data-driven research paradigms, aiming to provide theoretical guidance and technical references for the high-value utilization and modernization of lacquer resources. Full article

The growing demand for sustainable packaging materials has accelerated interest in biomass-derived carbon fillers as functional reinforcements for biodegradable polymer composites. This review critically evaluates the use of carbon materials produced from agricultural residues, particularly palm kernel shell (PKS) and coconut shell (CS), in biopolymer composite coating films for food packaging applications. Recent thermochemical conversion routes, including carbonization, activation, and catalytic graphitization, are discussed in relation to their influence on filler morphology, porosity, surface chemistry, and graphitic ordering. Particular emphasis is placed on structure–property relationships in composite systems containing matrices such as polylactic acid (PLA), starch, chitosan, gelatin, and polyvinyl alcohol (PVA). Published studies indicate that properly dispersed carbon fillers can improve tensile strength, thermal stability, ultraviolet shielding, and oxygen/water vapor barrier performance through stress-transfer mechanisms and tortuous diffusion pathways. However, excessive filler loading or poor interfacial compatibility frequently causes agglomeration, brittleness, and loss of transparency. Surface modification strategies including oxidation, silanization, and surfactant-assisted dispersion, are therefore reviewed as key approaches to optimize composite performance. Finally, current limitations involving migration safety, process scalability, and the lack of standardized testing protocols are discussed. Overall, PKS- and CS-derived carbon fillers represent promising sustainable additives for next-generation biopolymer composite packaging systems. Full article

Monoethanolamine (MEA) remains the predominant solvent for carbon dioxide (CO₂) capture due to its rapid reaction kinetics, substantial absorption capacity, and demonstrated industrial effectiveness. Despite its established status, MEA-based systems are undergoing continuous development to lower energy requirements, enhance solvent stability, and expand operational adaptability. This review provides a critical assessment of recent progress in MEA-based CO₂ capture, encompassing molecular-level understanding, advancements in reactor and process design, solvent modification strategies, and system-wide optimization. Recent theoretical and experimental research has improved the understanding of CO₂ absorption mechanisms in MEA, highlighting the effects of reaction-product buildup, interfacial phenomena, and free amine availability on mass-transfer efficiency. Reboiler duty and comparable work have significantly decreased as a result of advances in process intensification, improved regeneration systems, and energy-integration techniques. New hybrid strategies that partially decouple capture from thermal regeneration, such as combined absorption–mineralization pathways, show promise for long-term CO₂ sequestration. To address regeneration energy, corrosion, degradation, and cyclic stability, this review examines advances in MEA-based solvents, including aqueous blends, non-aqueous and biphasic systems, ionic liquids, and deep eutectic solvent hybrids. It also critically assesses the trade-offs of developments in intensified contactors, surfactants, nanomaterials, and catalysts. The growing role of digital optimization, machine learning, and computational modeling in MEA process design and control is highlighted. Overall, this analysis underscores MEA’s continued importance as a versatile platform for next-generation carbon capture, utilization, and storage. Full article

Electrokinetic-Permeable Reactive Barrier (EK-PRB) technology can effectively remediate heavy metal-contaminated soil, and the properties of PRB materials play an important role in determining the remediation efficiency. To select a suitable PRB material, montmorillonite (MMT) was modified using cetyltrimethylammonium bromide (CTAB), sodium dodecylbenzenesulfonate (SDBS), and cocamidopropyl betaine (CAB), respectively; their remediation efficiencies for soils co-contaminated with Zn²⁺, Pb²⁺, and Cd²⁺ were then compared within an EK-PRB system. The results indicated that remediation efficacy varied significantly depending on the heavy metal and the surfactant used for modification. After 7 days of remediation, SDBS-modified MMT achieved the highest Zn²⁺ removal efficiency (49.65%), whereas CTAB-modified MMT showed optimal removal performance for both Pb²⁺ (38.03%) and Cd²⁺ (76.02%). When the remediation time was extended to 14 days, SDBS-modified MMT attained the highest removal efficiencies for Zn²⁺ (69.80%) and Pb²⁺ (69.50%), while CTAB-modified MMT maintained superior Cd²⁺ removal performance (86.94%). Energy consumption analysis showed that both CAB- and SDBS-modified MMT reduced energy consumption moderately compared with the unmodified control, whereas CTAB modification resulted in a substantial increase in energy demand. Experimental results confirm that surfactant-modified MMT effectively optimizes the EK-PRB remediation. A comprehensive evaluation considering both removal efficiency and energy consumption identified SDBS-MMT as the optimal material. The optimized EK-PRB parameters established in this study provide theoretical and technical support for the remediation of soils co-contaminated with multiple heavy metals. Full article

Constructing efficient conductive networks in flexible polymer matrices remains a central challenge in electromagnetic interference (EMI) shielding material design. In this work, a ‘point-line’ hybrid filler system combining conductive carbon black (CB) and multi-walled carbon nanotubes (MWCNTs) was incorporated into a silicone rubber matrix to systematically engineer the conductive network architecture. By optimising the CB/MWCNT blending ratio, a composite with a tensile strength of 8.5 MPa, elongation at break of 180%, and EMI shielding effectiveness of 50 dB was achieved at a 1:1 weight ratio. Further surface modification of the hybrid fillers using five surfactants, including sodium dodecylbenzene sulfonate (SDBS), cetyltrimethylammonium bromide (CTAB), polyvinylpyrrolidone (PVP), nonylphenol ethoxylate (NPEO), and octylphenol ethoxylate (OPEO), was systematically investigated. OPEO modification was proved the most effective, improving EMI shielding performance to 58 dB while enhancing tensile strength by 11.8% and elongation at break by 50%. These results demonstrate that rational filler hybridisation combined with targeted surfactant modification offers a practical and scalable route to high-performance flexible EMI shielding composites. Full article

This study investigates the adsorption of ibuprofen (IBU) and diclofenac sodium (DS) using bentonite modified with varying amounts (50, 75, and 100% of cation exchange capacity—CEC) of two surfactants: octadecyl(dimethylbenzyl)ammonium (ODMBA) chloride and hexadecyltrimethylammonium (HDTMA) bromide. The resulting organobentonites were characterized by Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry/thermogravimetric analysis (DSC/TG), and zeta potential analysis. The results indicated that higher surfactant concentrations in organobentonites improved adsorption efficiencies for both drugs, while ODMBA-modified organobentonites exhibited notably larger adsorption capacities than HDTMA-modified samples. The adsorption isotherms fitted well to both the Langmuir and Freundlich models, with a better fit observed for the Freundlich model. The highest adsorption capacities were 102 mg/g for IBU and 160 mg/g for DS on sample OB-100 (organobentonite with 100% of ODMBA). Characterization of samples after drug adsorption, using FTIR, zeta potential and DSC/TG analysis, confirmed drug presence in organobentonites. Adsorption tests of DS in real river water (Danube and Sava rivers) showed that OB-100 demonstrated high removal capacity for DS. The findings suggest that organobentonites are low-cost adsorbents with potential for the removal of pharmaceutical contaminants from real aquatic environments. Full article

Ordered mesoporous silica (OMS) is widely investigated as a mineral carrier for bioactive compounds; however, the adsorption of poorly soluble flavonoids such as quercetin on unmodified silica remains limited, and the effect of cationic surfactant modification on adsorption performance is still insufficiently understood. This study evaluates the adsorption of quercetin on OMS modified with tetrabutylammonium bromide (TBA-Br) and hexadecyltrimethylammonium bromide (HDTMA-Br). Batch adsorption experiments were analyzed using various adsorption isotherm models, and the quality of fit was evaluated based on the coefficient of determination (R²) and the reduced chi-square statistic (χ²/DoF). The results indicated that quercetin adsorption followed a physisorption mechanism, predominantly governed by hydrophobic interactions and surface heterogeneity. Silica modified with HDTMA-Br exhibited a significantly higher maximum sorption capacity compared to OMS-TBA-Br, reaching g_max values of up to 5.2 mg·g⁻¹, whereas the maximum adsorption for OMS-TBA-Br did not exceed 4.2 mg·g⁻¹. The best fit of the experimental data was obtained for models accounting for the heterogeneous nature of the adsorbent surface, particularly the Tóth model. The obtained results clearly demonstrate that modification of OMS with a cationic surfactant possessing a long alkyl chain significantly enhances the adsorption capacity of silica toward quercetin, which is of considerable importance for the design of mineral carriers for bioactive compounds. Full article

Research on tannin-based foams has shown promising results. However, all developments in this field have not been addressed from different perspectives, in a systematic way, and with an emphasis on sustainability. This work discusses different formulations, emphasizing their bio-based components and how modifications influence key properties. It examines life cycle assessment (LCA) studies through a sustainability lens and identifies major commercial phenolic products to highlight the practical use of tannin foams for thermal insulation. The type of tannins, as well as their sources, influences the key properties of these foams. The replacement of formaldehyde, a crosslinking agent known for its health risks, is possible, particularly through more sustainable alternatives that allow for foams with better properties than those obtained with formaldehyde. Substitution of diethyl ether with less hazardous alternatives results in foams with improved thermal and mechanical performance. The elimination of the blowing agent—the green alternative—also leads to foams with good performance. The presence of additives (surfactants, plasticizers, and fillers), some of which are sustainable, improves the mechanical properties of the foams. The performance in fire-related applications, already promising, is also enhanced by the presence of additives. An increase in understanding, combined with the sustainable nature of the various alternatives, makes tannin-based foams promising candidates for next-generation insulation and structural materials in construction. Full article

This work reports the reuse of waste glass as a sustainable silica source for the synthesis of mesoporous silica, as an alternative to conventional silica precursors. Silica gel was produced through alkaline dissolution of glass powder using sodium hydroxide and subsequently employed as a precursor for the synthesis of porous silica. The waste-derived glass powder and the synthesized silica-based materials were characterized to assess their structural, morphological, surface, and textural properties. XRD analysis confirmed the amorphous nature of all samples, while FTIR spectra indicated successful silica network formation with modifications in bond connectivity. SEM imaging revealed spherical particles with average diameters of approximately 0.19 ± 0.02 µm for silica gel and 0.15 ± 0.03 µm for the mesoporous silica. Zeta potential measurements indicated a negative surface charge and good colloidal stability in aqueous media. Nitrogen sorption analysis revealed that the specific surface area was limited by the low solubility of silica gel in acidic media, which prevents ideal condensation on the surface of surfactant micelles. The results demonstrate that waste glass-derived silica gel is a promising precursor, although the synthesis conditions did not yield a highly ordered mesostructure, highlighting the need for further control of precursor solubility and pH. Full article

The development of effective inhalable drugs remains a key challenge in the treatment of pulmonary diseases, due to the physiological barriers of the respiratory tract and the lack of predictive models that accurately reproduce the human lung environment. In this context, liposomes (LP) have emerged as promising nanocarriers for pulmonary drug delivery due to their high biocompatibility, surfactant-like composition, capacity to encapsulate both hydrophilic and lipophilic drugs, and potential to provide sustained drug release while reducing systemic toxicity. This study evaluates the influence of size and PEGylation on their physicochemical properties, cytotoxicity, interaction with the pulmonary mucus, and cellular internalisation. LP of 100 nm (LP 100), 200 nm (LP 200), and 600 nm (LP 600) were characterised physiochemically and evaluated in pulmonary cell lines (A549 and Calu-3) exposed in liquid–liquid interface (LLI) and air–liquid interface (ALI) by nebulisation. In addition, artificial pulmonary mucus (APM) was employed to analyse LP penetration through the pulmonary mucus barrier. Results indicate that LP 100 exhibits greater colloidal stability, lower cytotoxicity, and sustained migration through the APM over time with respect to larger particles. PEGylation of LP 100 (LP-PEG) further increases their stability and ability to penetrate the APM, although cellular internalisation is reduced due to the steric effect of the PEG coating. These findings highlight the importance of adjusting the size and surface modifications of LPs according to the therapeutic target of the drug, optimising their persistence on the epithelial surface or their cellular uptake. Full article

This study aimed to design a new composite with promising antimicrobial and antioxidant properties by a simple modification process of natural bentonite (B) with polysaccharide chitosan isolated from edible mushrooms Agaricus bisporus—ChM (sample B–ChM) and subsequently with a cationic surfactant—hexadecyltrimethylammonium bromide—HB (sample B–ChM–HB) for effective removal of mycotoxin zearalenone (ZEN). Characterization confirmed the presence of ChM in B–ChM and both ChM and HB in B–ChM–HB. Compared to non- or slightly inhibitory activity of B and B–ChM, B–ChM–HB showed fungicidal activity against yeast Candida albicans and mycotoxigenic mold Aspergillus flavus, with a reduction of 6.00 log10 (CFU/mL) and 5.32 log10 (CFU/mL), respectively. B–ChM–HB showed a very high neutralization ability on •DPPH (89.03%–95.99%) in the concentration range of 0.625–5.0 mg/mL, the highest ferrous ion chelating ability (80.25%) at a concentration of 0.625 mg/mL, and did not induce lipid peroxidation in the linoleic acid model system. While B and B–ChM exhibited low adsorption of ZEN, its adsorption by B–ChM–HB was significantly higher. The equilibrium results of B–ChM–HB for ZEN were in accordance with the linear isotherm model at pH 3 and 7, pointing out that hydrophobic interactions (partitioning process) were relevant for toxin adsorption by the composite. Similar maximum ZEN adsorbed amounts under the applied experimental conditions (14.4 mg/g) at both pH values suggested that its adsorption was independent of the pH. This study reported for the first time that a novel composite of B with ChM and HB showed promising antimicrobial and antioxidant properties and was an efficient adsorbent for mycotoxin ZEN. Full article

Microbial biosurfactants (mBSs) are bioactive molecules with diverse applications, notably as antimicrobial agents against antibiotic-resistant pathogens. Produced by bacteria and yeasts, mBSs are classified as glycolipids, lipopeptides, polymeric, and particulate types. The global rise in multidrug-resistant organisms, such as Escherichia coli, Klebsiella pneumoniae, Salmonella typhimurium, Pseudomonas aeruginosa, and Acinetobacter baumannii, underscores the urgent need for new antimicrobial strategies. mBSs disrupt microbial growth by interacting with the lipid components of pathogens, offering promising alternatives to conventional antibiotics. This review highlights the sources, chemical structures, and properties of mBSs, their antimicrobial activities, synergistic effects with antibiotics, and structure–activity relationships. Special emphasis is placed on surfactant modification, where targeted changes—such as valine substitution in surfactin—significantly lower critical micelle concentrations (CMC) and enhance antimicrobial potency. Such rational engineering demonstrates how biosurfactants can be tailored for improved biomedical performance while minimizing cytotoxicity. In parallel, artificial intelligence (AI) algorithms, including artificial neural networks and genetic algorithms, optimize yields, predict substrate suitability from agricultural residues, and guide microbial strain engineering. AI models can predict interfacial behavior and synchronize fermentation with purification. Advancing the understanding of mBS interactions with microbial membranes, combined with modification strategies and AI-guided optimization, is essential for developing targeted therapies against resistant infections. Future research should integrate these approaches to engineer novel derivatives, reduce costs, and validate clinical potential through comprehensive in vivo studies. Full article