Search Results (1,637)

The threats leading to the extinction of humanity accelerate the evolution and development of materials that are capable of providing conditions for preserving health and, implicitly, life. In our work, we developed drug delivery systems based on mesoporous silica which can deliver an antibiotic, bacitracin, in a more controlled manner. The synthesis of the FDU-12 was performed through a sol–gel method and alternatively functionalized with -NH₂ groups or with poly(N-acryloylmorpholine) chains. The loading of bacitracin was performed using the vacuum-assisted method we successfully used to load these mesoporous materials preferentially within the pores as proved by the TGA-DSC results. The release was performed in two types of simulated body fluid (SBF) and this process was evaluated with chromatographic method using UV detection. The obtained data were fitted in three mathematical models of kinetic drug release (Weibull model, Korsmeyer–Peppas model, and nonlinear regression). The antimicrobial evaluation demonstrated that bacitracin-loaded FDU-12 formulations exhibited strong activity against both reference and clinical Staphylococcus strains. At sub-inhibitory concentrations, all formulations significantly reduced microbial adherence and biofilm formation, although certain strain-dependent stimulatory effects were observed. Furthermore, exposure to sub-MIC levels modulated the production of soluble virulence factors (hemolysins, lipase, and amylase), in a formulation- and strain-dependent manner, underscoring the ability of surface-functionalized FDU-12 carriers to influence bacterial pathogenicity while enhancing antimicrobial efficacy. Full article

Hydrogen-based energy systems require large amounts of high-purity water, motivating thermally driven desalination that can recover low-grade heat. This study evaluates a silica gel–water adsorption chiller–desalination unit as a coupled source of cooling and pre-treated water for electrolysers. A laboratory two-bed system was tested on saline feed using 300 s valve-switching periods at an 80 °C driving temperature and 20–30 °C cooling water. Dynamic vapour sorption measurements provided Dubinin–Astakhov equilibrium and linear driving force kinetic parameters, implemented in a CFD porous bed model via user-defined source terms. Experiments yielded COP values of 0.29–0.41, an SCP of 165 W·kg⁻¹ of adsorbent, and an average distillate production of 1.68–1.82 kg·h⁻¹, while distillate conductivity remained ≈2.3 μS·cm⁻¹. The model reproduced the mean condensate production with a ≈6% underprediction. It was then used to compare six alternative fin geometries with a constant heat-transfer area. Fin-shape modifications changed inter-fin heating by <2 K and cumulative desorbed mass by <0.05%, indicating limited sensitivity to subtle local refinements. Performance gains are more likely to arise from operating conditions and exchanger-scale architecture than from minor fin-shape changes. Full article

In recent years, diagnostic technologies that utilize noninvasively collected sweat have garnered significant interest. However, the concentration of components in sweat is lower than that in blood, making the introduction of a concentration step as a sample pretreatment crucial for achieving highly sensitive detection. In this study, we developed a PDMS-based microchannel filled with silica gel, a desiccant particle, to concentrate liquid samples at room temperature without requiring an external power source or heating. The evaluation of the basic characteristics of the fabricated microchannel confirmed that filling it with silica gel efficiently removed the solvent vapor from the liquid samples. In concentration tests using the fluorescent dye uranine as a model for sweat sugar, a maximum 1.4-fold concentration was achieved in DPBS solution and a 1.2-fold concentration in artificial sweat at room temperature. In contrast, no similar concentration effect was observed in microchannels without silica gel packing. The proposed silica-gel-packed PDMS microchannel features a simple structure and requires no external equipment, making it easily integrable with existing microfluidic devices as a sample pretreatment module. This method is considered useful as a passive and simple sample concentration technique for the analysis of low-molecular-weight components in sweat. Full article

The emulsification of a molten fusible metal alloy in a liquid epoxy matrix with its subsequent curing is a novel way to create a highly concentrated phase-change material. However, numerous challenges have arisen. The high interfacial tension between the molten metal and epoxy resin and the difference in their viscosities hinder the stretching and breaking of metal droplets during stirring. Further, the high density of metal droplets and lack of suitable surfactants lead to their rapid coalescence and sedimentation in the non-cross-linked resin. Finally, the high differences in the thermal expansion coefficients of the metal alloy and cross-linked epoxy polymer may cause cracking of the resulting phase-change material. This work overcomes the above problems by using nanosilica-induced physical gelation to thicken the epoxy medium containing Wood’s metal, stabilize their interfacial boundary, and immobilize the molten metal droplets through the creation of a gel-like network with a yield stress. In turn, the yield stress and the subsequent low-temperature curing with diethylenetriamine prevent delamination and cracking, while the transformation of the epoxy resin as a physical gel into a cross-linked polymer gel ensures form stability. The stabilization mechanism is shown to combine Pickering-like interfacial anchoring of hydrophilic silica at the metal/epoxy boundary with bulk gelation of the epoxy phase, enabling high metal loadings. As a result, epoxy shape-stable phase-change materials containing up to 80 wt% of Wood’s metal were produced. Wood’s metal forms fine dispersed droplets in epoxy medium with an average size of 2–5 µm, which can store thermal energy with an efficiency of up to 120.8 J/cm³. Wood’s metal plasticizes the epoxy matrix and decreases its glass transition temperature because of interactions with the epoxy resin and its hardener. However, the reinforcing effect of the metal particles compensates for this adverse effect, increasing Young’s modulus of the cured phase-change system up to 825 MPa. These form-stable, high-energy-density composites are promising for thermal energy storage in building envelopes, radiation-protective shielding, or industrial heat management systems where leakage-free operation and mechanical integrity are critical. Full article

This study investigated the effects of incorporating rice husk ash (RHA) as a partial replacement for cement on the properties of concrete. To determine the optimal replacement level, RHA was used to replace cement in varying proportions, ranging from 0% to 25% in 5% increments. The mix with 0% RHA served as the control. The properties evaluated included setting time, density, and compressive strength. The results revealed that blending RHA with cement increased the initial setting time. This was attributed to the lower calcium oxide (CaO₂) content of RHA, which slows early-age hydration reactions. Conversely, the final setting time was reduced due to the pozzolanic activity of RHA, which enhances later-stage reactions. Additionally, the inclusion of RHA resulted in a decrease in concrete density, owing to its lower specific gravity and bulk density compared to Portland cement. Despite this, RHA-modified specimens exhibited higher compressive strengths than the control specimens. This strength enhancement was linked to the formation of additional calcium–silicate–hydrate (C-S-H) gel due to the pozzolanic reaction between amorphous silica in RHA and calcium hydroxide (CaOH) from hydration reaction. The gel fills concrete voids at the microstructural level, producing a denser and more compact concrete matrix. Based on the balance between strength and durability, the optimal RHA replacement level was identified as 10%. Full article

Adsorption chillers can produce chilled and desalinated water using low-grade heat, but their performance is limited by low coefficient of performance (COP) and large system mass. Enhancing heat and mass transfer in the sorbent bed is key to improving efficiency. This work introduces and systematically evaluates binder-stabilized silica gel composites as a structural and thermal enhancement strategy for adsorption chillers. Silica gel composites bonded with epoxy resin and polyvinyl alcohol (PVA) were evaluated for adsorption chiller applications. Thermal stability, conductivity, microstructure, equilibrium sorption, and sorption hysteresis were assessed. The results indicate that PVA-based composites were thermally unstable and discarded, whereas epoxy-bonded silica gel showed high thermal stability and mechanically robust granules with preserved pore connectivity. The epoxy composite exhibited 109% higher thermal conductivity than loose silica gel, improving internal heat transfer. This improvement is accompanied by a reduction in sorption capacity of approximately 58%, attributable to the inert resin fraction. Notably, the composite exhibits a reduced and locally negative sorption hysteresis, indicating facilitated desorption and lowered internal diffusion resistance. The epoxy-bonded silica gel therefore provides a promising combination of thermal stability, improved heat transfer, and enhanced sorption–desorption behaviour, supporting its potential to increase the efficiency of next-generation adsorption chillers. Full article

Silica-based sorbents covalently modified with polyhedral boron clusters represent a promising platform for highly selective separation materials, yet robust and synthetically accessible immobilization protocols remain underdeveloped. In this work, novel sorbents based on commercially available silica gels functionalized with closo-dodecaborate anions were synthesized and systematically characterized. Two immobilization strategies were compared: direct nucleophilic addition of surface aminopropyl groups to the nitrilium derivative (Bu₄N)[B₁₂H₁₁NCCH₃] and sol–gel condensation of a pre-formed boron-containing APTES-derived silane. Covalent attachment via amidine bond formation was confirmed by solution and MAS ¹¹B NMR spectroscopy, IR spectroscopy, elemental analysis/ICP-OES, and SEM. The direct grafting route afforded a boron loading of 4.5 wt% (≈20% of the theoretical capacity), with the efficiency limited by electrostatic repulsion between anionic amidine fragments on the negatively charged silica surface, whereas the APTES route gave lower absolute loading (0.085 mmol/g) due to the low specific surface area of the coarse silica support. Despite the moderate degree of functionalization, the resulting boron cluster–modified silica gels are attractive candidates for specialized chromatographic applications, where the unique hydrophobic and dihydrogen-bonding properties of closo-dodecaborates may enable selective retention of challenging analytes and motivate further optimization of surface morphology and immobilization conditions. Full article

Siraitia grosvenorii (Swingle) C. Jeffrey is widely recognized for its anti-inflammatory properties, as well as its roles in lung purification, phlegm elimination, intestinal function regulation, and anti-tumor activity. Its pharmacological activity is attributed to a diversity of functional components. However, due to the extensive application of sweet glycosides in food additives, there have been few studies on non-sweet glycosides, particularly those with high polarity. This paper investigates the chemical constituents in the non-sweet glycosides fraction of S. grosvenorii juice. First, an MCI GEL CHP20P chromatographic column was utilized to enrich the non-sweet glycosides fraction. Furthermore, two-step medium-pressure liquid chromatography (MPLC) was performed for the efficient preparative separation of high-polarity non-sweet glycosides with similar structures, using C18 and silica gel as stationary phases, respectively. Seven non-sweet glycoside compounds were identified through NMR and mass spectrometry analyses, including three new compounds (4-hydroxyphenylethanol 4-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranoside, 4-hydroxyphenylethanol 4-O-β-D-glucopyranosyl-(1→2)-β-D-glucopyranosyl-(1→6)-β-D-glucopyranoside and n-butanol 1-O-β-D-glucopyranosyl-(1→2)-β-D-glucopyranosyl-(1→6)-β-D-glucopyranoside), as well as four known ones (α-D-glucopyranosyl-(1→4)-D-glucose, α-D-glucopyranosyl-(1→2)-β-D-fructofuranoside, methoxy hydroquinone diglucoside, and β-D-glucopyranoside). The results demonstrate that mixed-mode MPLC using different stationary phases is an efficient approach for separating non-sweet glycosides from S. grosvenorii. Full article

Mugwort (Artemisia princeps Pamp.) is a traditional herb widely used across East Asia; despite this, optimal processing methods to preserve its functional components and palatability have not been fully established. Thus, we aimed to, for the first time, systematically examine the effects of 16 processing methods that combine blanching (steaming or boiling), drying [freeze-drying (FD), mechanical drying, shade drying, or silica gel drying], and rolling on mugwort’s appearance, total polyphenol content (TPC), antioxidant activity, and sensory characteristics. Our results showed that steaming for ≥2 min followed by FD was the most effective method for maintaining a high TPC and a vibrant green color. In contrast, boiling with sodium bicarbonate preserved color but substantially reduced both TPC and chlorogenic acid (CGA) content compared with steaming. Sensory evaluation revealed that consumers consistently preferred steaming over other processing methods. Liquid chromatography–tandem mass spectrometry analysis revealed that prolonged drying induced CGA isomerization to neochlorogenic acid. Moreover, processing time substantially influenced CGA stability, while high TPC did not compromise mugwort flavor. Our findings imply that an optimized combination of steaming and FD maximizes both functional and sensory quality of mugwort, highlighting the potential of mugwort tea as a flavorful functional food. Full article

This study examines how the Alkali–Silica Reaction (ASR) modifies chloride transport and chloride-induced corrosion (CIC) in reinforced concrete beams. Non-reactive and reactive concrete beams were cast with blue metal and dacite aggregates and subjected to a two-stage exposure: (i) alkali-rich immersion at 38 °C to induce ASR, and (ii) impressed-current CIC and NT BUILD 492 chloride migration testing. Microstructural changes were characterized using SEM–EDS and TGA. The reactive specimens developed extensive surface cracking, but after one year of ASR exposure, exhibited 47–53% lower non-steady-state migration coefficients (Dnssm: 7.03–8.02 × 10⁻¹² m²/s) than the non-reactive beam (15.09 × 10⁻¹² m²/s). After two years, Dnssm was reduced by approximately 37–56% (4.78–6.93 vs. 10.92 × 10⁻¹² m²/s). Crack mapping confirmed higher crack density and width in reactive beams, while SEM–EDS and TGA evidenced Ca depletion and the formation of C–(N,K)–S–H gels, which fill cracks and refine the pore structure. Electrical resistance monitoring showed earlier corrosion initiation in ASR-damaged beams but less pronounced resistance loss during the propagation phase. Overall, the results indicate that ASR can initially accelerate corrosion initiation through microcracking and reduced resistivity, but long-term gel deposition can partially seal transport paths and lower chloride migration under the specific conditions of this study. Full article

Growing cooling demand and environmental concerns motivate research into alternative technologies capable of converting low-grade heat into useful cooling. This study proposes a regression-assisted multi-objective optimisation framework using the Ant Lion Optimiser and its multi-objective variant to jointly maximise the coefficient of performance (COP), cooling capacity ($Q_{cc}$) and waste-heat recovery efficiency (${\eta }_e$). Pareto-optimal solutions exhibit a one-dimensional ridge in which ${\eta }_e$ declines, and COP and $Q_{cc}$ increase simultaneously. Within the explored bounds, non-dominated ranges span COP = 0.674–0.716, $Q_{cc}=$ 18.3–27.5 kW and ${\eta }_e=$ 0.118–0.127, with a practical compromise near COP ≈ 0.695, $Q_{cc}$ ≈ 24 kW and ${\eta }_{e }\approx$0.122–0.123. Compared to the typical reported COP band for single-stage silica-gel/water ADCs, the practical compromise solution (COP ≈ 0.695) offers a conservative COP improvement of approximately 16% when benchmarked against COP = 0.6, while the compromise $Q_{cc}$ ($Q_{cc}$ ≈ 24 kW) represents a conservative increase of approximately 20% relative to the upper product-class reference (20 kW). A one-at-a-time sensitivity analysis with re-optimisation identifies the hot- and chilled-water inlet temperatures and exchanger conductance as the dominant decision variables and maps diminishing-return regions. This framework can effectively utilise low-grade heat in future low-carbon buildings and processes, supporting the configuration of ADC systems. Full article

The construction industry faces growing pressure to adopt sustainable materials due to the high CO₂ emissions associated with ordinary Portland cement (OPC) production. Geopolymers synthesized from industrial by-products such as fly ash offer a promising low-carbon alternative. However, the extensive use of commercial sodium silicate (SSC) as an activator remains constrained by its high cost and energy-intensive manufacturing. This study investigates a silica fume-derived sodium silicate alternative (SSA) combined with NaOH as a more sustainable activator for fly ash-based geopolymer mortar. Mortars were prepared with alkali activator-to-precursor (AA/P) ratios of 0.7 and 0.5 and cured at 65 °C and 80 °C. SSA-based mixes exhibited comparable flowability to SSC-based mortars, with slightly longer setting times making them favorable for placement. Mechanical tests showed the superior performance of SSA systems, with AS0.7-65 achieving the highest compressive strength and AS0.7-80 demonstrating greater flexural and tensile strength. Microstructural analyses (SEM, EDX, ATR-FTIR) revealed denser matrices and enhanced sodium aluminosilicate hydrate (N-A-S-H) and calcium-rich N(C)-A-S-H gel formation. Economic assessment indicated approximately 30% cost reduction and a modest (~2%) decrease in CO₂ emissions. These findings highlight SSA as a technically viable and sustainable activator for next-generation geopolymer construction. Full article

The integration of silica nanoparticles (NS) into cementitious composites has emerged as a promising strategy to refine the microstructure and enhance concrete performance. Beyond their chemical role in accelerating hydration and promoting additional C–S–H gel formation, silica nanoparticles act as physical fillers, reducing porosity and improving interfacial bonding within the matrix. These dual effects result in a denser and more resilient composite, whose mechanical and dynamic responses differ from those of conventional concrete. However, studies addressing the vibrational and modal behavior of nano-reinforced concretes, particularly under elastic and viscoelastic foundation conditions, remain limited. This study investigates the dynamic response of NS-reinforced concrete slabs using a refined quasi-3D plate deformation theory with five (05) unknowns. Different foundation configurations are considered to represent various soil interactions and assess structural integrity under diverse supports. The effective elastic properties of the nanocomposite are obtained through Eshelby’s homogenization model, while Hamilton’s principle is used to derive the governing equations of motion. Navier’s analytical solutions are applied to simply supported slabs. Quantitative results show that adding 30 wt% NS increases the Young’s modulus of concrete by about 26% with only ~1% change in density; for simply supported slender slabs, this results in geometry-dependent increases of up to 18% in the fundamental natural frequency. While the Winkler and Pasternak foundation parameters reduce this frequency, the damping parameter of the viscoelastic foundation enhances the dynamic response, yielding frequency increases of up to 28%, depending on slab geometry. Full article

Objective: The objective of our study was to synthesize and characterize silica–copper nanomaterials and to evaluate their biological properties (antibacterial, redox, cytotoxic, and ecotoxic) for potential applications. Methods and Results: Si/Cu-based materials were prepared by a sol–gel method. They were characterized by XRD, UV-Vis, and SEM-EDS. The antibacterial activity of the materials was evaluated against Gram-positive bacteria (Staphylococcus aureus, Bacillus cereus), Gram-negative bacteria (Escherichia coli, Pseudomonas aeruginosa, Salmonella typhimurium), and yeasts (Candida albicans, Saccharomyces cerevisiae). The nanomaterial that was calcined at 500 °C exhibited greater antibacterial efficacy compared to the gel form. S. typhimurium demonstrated the highest susceptibility, whereas S. aureus and P. aeruginosa were the most resistant of the tested bacteria. Both yeasts exhibited comparable sensitivity (MBC = 1.0 mg/mL). The redox activity of both nanomaterials was tested at pH 7.4 (physiological) and 8.5 (optimal) by the activated chemiluminescent method. The nanocomposites significantly inhibited the free-radical and ROS generation. This presents them as redox regulators in living systems. The cytotoxic effects in normal BEAS-2B and tumor A549 human cell lines were assessed microscopically and by the cell viability neutral red uptake assay, CC₅₀ being evaluated. The observed effects suggest moderate, similar cytotoxicity in both cell lines. The ecotoxicity study using Daphnia magna showed an LC₅₀ of ~7–8 mg/L about Si/Cu/500. The LC₅₀ for Si/Cu (gel) was lower than 0.25 mg/L, indicating an increase in toxicity with increased exposure time. Conclusions: Possible applications of the newly synthesized nanomaterials include antimicrobial coatings, drug delivery systems, antioxidant additives in various formulations, and water purification. Full article

Hybrid silica xerogels functionalised with chlorinated organosilanes combine tunable porosity and surface chemistry, rendering them attractive for applications in sensing, membrane technology, and photonics. This study quantitatively investigates the thermal decomposition kinetics of organochlorinated xerogels and correlates with volatile compounds previously identified via Thermogravimetric Analysis (TGA) coupled to Fourier-Transform Infrared Spectroscopy (FT–IR) and Gas Chromatography coupled with Mass Spectrometry (GC–MS). The xerogels were synthesised via the sol–gel process using organochlorinated alkoxysilane precursors and yielded highly condensed nanostructures in which the precursor nature strongly influences the morphology and textural properties. In this study, the molar percentage of the organochlorinated compounds was fixed at 10%. Standard N₂ adsorption-desorption isotherm at 77 K revealed that increasing the precursor content systematically decreased the specific surface area and pore volume of the materials while promoting the formation of periodic domains, which are observed even at low organosilane molar percentages. Thermal characterisation via TGA/FT–IR/GC–MS revealed at least two main decomposition stages, with thermal stability following the order of 4–chlorophenyl > chloromethyl > 3–chloropropyl > 2–chloroethyl. This study focuses on kinetic and mechanistic insights in the thermal decomposition process through the Flynn–Wall–Ozawa isoconversional method and Criado master plots, using TGA/Differential Scanning Calorimetry (DSC) measurements under nitrogen at multiple heating rates (5, 10, 20, 30, and 40 K min⁻¹), which revealed activation energies ranging from 53 to 290 kJ mol⁻¹. Demonstrating that the chlorinated organosilane precursor directly controls both the textural properties and thermal behaviour of the resulting silica materials, with aromatic groups providing superior thermal stability compared to aliphatic chains. These quantitative kinetic insights provide a predictive framework for designing thermally stable hybrid materials while ensuring safe processing conditions to prevent hazardous volatile release. Full article