Uniform Size Research Articles

Nano-Reactors Based on Ovotransferrin Organic Skeleton through a Ferroptosis-like Strategy Efficiently Enhance Antibacterial Activity.

The issue of bacterial resistance is an escalating problem due to the misuse of antibiotics worldwide. This study introduces a new antibacterial mechanism, the ferroptosis-like death (FLD) of bacteria, and an approach to creating green antibacterial nano-reactors. This innovative method leverages natural iron-containing ovotransferrin (OVT) assembled into an organic skeleton to encapsulate low-concentration adriamycin (ADM) for synthesizing eco-friendly nano-reactors. FLD utilizes the Fenton reaction of reactive oxygen species and ferrous ions to continuously produce ·OH, which can attack the bacterial cell membrane and destroy the cell structure to achieve bacteriostasis. The OVT@ADM nano-reactors are nearly spherical, with an average diameter of 247.23 nm and uniform particle sizing. Vitro simulations showed that Fe3+ in OVT@ADM was reduced to Fe2+ by glutathione in the bacterial periplasmic space, which made the structure of OVT loose, leading to a sustained slow release of ADM from OVT@ADM. The H2O2 continuously produced by ADM oxidized Fe2+ through the Fenton reaction to produce ·OH and Fe3+. The results of the antibacterial assay showed that OVT@ADM had a satisfactory antibacterial effect against S. aureus, and the inhibition rate was as high as 99.3%. The cytotoxicity results showed that the mitigation strategy significantly reduced the cytotoxicity caused by ADM. Based on the FLD mechanism, OVT@ADM nano-reactors were evaluated and applied to bacteriostasis. Therefore, the novel antibacterial mechanism and OVT@ADM by the green synthesis method have good application prospects.

Preparation of KH560‐UiO‐66‐NH2/Pebax mixed matrix membranes and CO2 separation

AbstractMetal–organic frame UiO‐66‐NH2 was modified by 3‐glycidyl ether oxypropyl trimethoxysilane (KH560), and KH560‐UiO‐66‐NH2 was synthetized and added to Pebax to prepare KH560‐UiO‐66‐NH2/Pebax mixed matrix membranes (MMMs). The epoxy group of KH560 had an amine‐epoxidation reaction with the NH2 in UiO‐66‐NH2, which prevented UiO‐66‐NH2 from agglutinating in the MMMs. In addition, the NH bond and OH bond of KH560‐UiO‐66‐NH2 could theoretically form hydrogen bonds with CO and NH bonds in the main chain of polymerization, respectively, so as to improve the interfacial compatibility between fillers and polymers. The structure and properties of the filler particles and MMMs were evaluated by Fourier transform infrared spectrometer, x‐ray diffraction, scanning electron microscopy, and thermogravimetric analyzer. The results showed that the filler particles were successfully synthesized, and had good crystallinity, uniform size distribution, and good thermal stability. The inorganic and organic interfaces of MMMs had no obvious interface defects. The obtained KH560‐UiO‐66‐NH2/Pebax MMMs showed CO2 permeability of 111.52 Barre and CO2/N2 selectivity of 92.16, which were 85.65% and 88.73% higher than that of pristine membranes, respectively. The gas separation performance of MMMs was significantly improved, exceeding the upper bound of 2008 Robeson.

What matters for drug delivery to tumor by nanoparticles: Gaining insights from PBPK/PD simulation of drug nanocrystals

Background and purpose: In our previous studies, drug nanocrystals were directly prepared by solution crystallization, possessing uniform particle size and morphology suitable for intravenous (IV) injection. These nanocrystals accumulated in a small percentage of their injected dose in tumor-bearing mice but showed similar anti-tumor effectiveness and much-reduced side effects compared with current commercial solubilized and encapsulated delivery systems. Experimental approach: In this study, we aimed to delineate possible controlling factors for the pharmacokinetics (PK) and biodistribution behaviors of paclitaxel (PTX) nanocrystals tested in mice by applying physiologically based pharmacokinetics (PBPK) modeling, coupled with pharmacodynamics (PD) simulation, to the data. Key Results: Our results show that clearance of the drug plays a significant, if not the most important, role in determining tissue distribution, including tumor accumulation of PTX nanocrystals. Surface treatment of drug nanocrystals with polymeric surfactants also appeared to affect PK profiles and PD outcomes. Importantly, when scaled to model human parameters, our PK/PD simulations suggest that drug distribution in humans, as opposed to animal models, was significantly influenced by tissue partitioning rather than drug clearance. This finding could facilitate the design and development of future drug delivery systems. Conclusion: Drug nanocrystals deposited in tissues, including tumors, could therefore act as depots, releasing the drug back into the circulation, possibly contributing to extended treatment, as well as any detrimental effects.

Efficient preparation of cellulose nanocrystals and regulation of cholesteric liquid crystals for advanced anti‐counterfeiting

AbstractCellulose nanocrystals (CNCs) can self‐assemble to form cholesteric liquid crystal, which make it one of the most promising optical materials at present. CNCs can be produced by sulfuric acid hydrolysis. It is found that hydrolysis conditions influence the existing form of reaction components and their reaction activities, which leads to different reaction routes and mechanisms under varied reaction conditions, with CNCs of varied quality produced. High‐quality CNC with more uniform particle size could be prepared at a critical acid concentration of 64 wt%, which was used to study the formation process of CNC liquid crystal and the structure regulation of cholesteric liquid crystal. By adjusting the drying temperature and adding a small molecule of water‐soluble chitosan (WSC) can well regulate cholesteric liquid crystal and change the pitch of a film, and the reflection wavelength can be redshifted, thus enriching texture patterns and creating distinctive color. Suitable addition of WSC can enhance the multi‐domain effect during liquid crystal formation process and finally creates more colorful film with fine texture. The rich and tunable liquid crystal characteristics endowed by WSC addition is irreplicable and artistic, which helps to realize the great potential application of the composite film in advanced anti‐counterfeiting.

Optimized Ammonia-Sensing Electrode with CeO2/rGO Nano-Composite Coating Synthesized by Focused Laser Ablation in Liquid.

This study investigated the synthesis of cerium oxide (CeO2) nanoparticles (NPs) and composites with reduced graphene oxide (rGO) for the enhanced electrochemical sensing of ammonia. CeO2 NPs were prepared by the focused laser ablation in liquid (LAL) method, which enabled the production of high-purity, spherical nanoparticles with a uniform dispersion and sizes under 50 nm in a short time. The effects of varying irradiation fluence and time on the nanoparticle size, production yield, and dispersion were systematically studied. The synthesized CeO2 NPs were doped with rGO to form CeO2/rGO composites, which were drop casted to modify the glassy carbon electrodes (GCE). The CeO2/rGO-GCE electrodes exhibited superior electrochemical properties compared with single-component electrodes, which demonstrated the significant potential for ammonia detection, especially at a 4 J/cm2 fluence. The CeO2/rGO composites showed uniformly dispersed CeO2 NPs between the rGO sheets, which enhanced the conductivity, as confirmed by SEM, EDS mapping, and XRD analysis. Cyclic voltammetry data demonstrated superior electrochemical activity of the CeO2/rGO composite electrodes, with the 2rGO/1CeO2 ratio showing the highest current response and sensitivity. The CV response to varying ammonia concentrations exhibited a linear relationship, indicating the electrode's capability for accurate quantification. These findings highlight the effectiveness of focused laser ablation in enhancing nanoparticle synthesis and the promising synergistic effects of CeO2 and rGO in developing high-performance electrochemical sensors.

Production of 5-fluorouracil-loaded PLGA nanoparticles with toroidal microfluidic system and optimization of process variables by design of experiments

In recent decades, microfluidics has presented new opportunities for the production of nanoparticles (NPs). However, to achieve rapid clinical translation, the production of PLGA NPs in a single microfluidic channel for both the pharmaceutical research and industry without the need for scaling is still limited. The aim of this study was to accomplish the production of reproducible and stable 5-FU loaded Poly(lactic-co-glycolic acid) (PLGA) NPs, using an innovative toroidal microfluidic system, for cancer therapy. The toroidal microfluidic system enabled the production of spherical NPs ranging from 100 to 150 nm by adjusting both the TFR within the range of 5–15 mL/min and FRR between 1:3 and 1:7. A systematic assessment of critical process variables (total flow rate; TFR, flow rate ratio; FRR) for the production of PLGA NPs was conducted using Design of Experiment (DoE). The NPs, which exhibit a uniform size distribution, remained stable even after centrifugation and storage for 3 months at 4 °C. The encapsulation efficiency of drug and the concentration of NPs were not affected by changing process parameters. The effective 5-FU encapsulation into NPs resulted in a controlled in vitro drug release. Due to the controlled release profile of the 5-FU loaded PLGA NPs, the formulation was a promising candidate for mitigating the toxic side effects of free 5-FU and improving cancer treatment. In conclusion, toroidal microfluidic system enables high-volume production of stable PLGA NPs, both with and without 5-FU.

Effects of Zr, Al, and Al+Zr Addition on Phase Evolution Characteristics and Strengthening Mechanisms of Fe‐42Ni‐2Y2O3 Oxide Dispersion Strengthening Steels Developed by Mechanical Alloying and Spark Plasma Sintering

In the present study, Fe‐42 wt% Ni‐2 wt% Y2O3 super‐invar‐based steels have been explored to study the effects of Zr, Al, and Zr+Al addition on phase evolution, strengthening mechanisms, and mechanical behavior. Three different compositions, such as Fe‐42Ni‐2Y2O3‐2Zr (2YZr), Fe‐42Ni‐2Y2O3‐2Al (2YAl), and Fe‐42Ni‐2Y2O3‐2Zr‐2Al (2YAlZr), are developed by mechanical alloying (MA) followed by spark plasma sintering (SPS) at 1100 °C with an applied pressure of 60 MPa. The 2YZr alloy after SPS shows the evolution of a uniform grain size of ≈1.7 μm, whereas 2YAl reveals the formation of bimodal grain structure sintered under the same condition. Conversely, the combined effect of Al and Zr addition results in the evolution of ultrafine grained structure (≈380 nm) after SPS at the same condition (i.e., at 1100 °C). The superior mechanical strength of the 2YAlZr alloy (5.3 GPa/1415 MPa) is attributed to the evolution of uniformly dispersed extremely fine (60 nm) high‐density Al‐ and Zr‐rich oxide complexes in the ultrafine grained matrix. The analysis of strengthening contributions to the yield strength is found to be correlated well with the experimental results and attributed to the morphology of microstructural constituents, their stability, and volume fraction of dispersoids in the matrix.

The conformational modification of myofibrillar protein by magnetic field improves its emulsification properties

This study investigated the effect of different magnetic field treatments (0, 3, 6, 9, 12 mT) on the structure and emulsification properties of myofibrillar protein (MP). The results showed that the emulsion stabilized by MP with 3, 6, 9 mT magnetic field treatments possessed higher emulsifying ability, storage stability and apparent viscosity, since magnetic field induced the structural unfolding of MP and exposed the hydrophobic groups (the surface hydrophobic increased from 30.10 to 43.73 μg). Meanwhile, the magnetic field treatments decreased the MP particle size from 1752.00 to 1278.67 nm, which was favorable for the diffusion and adsorption of proteins at the oil-water interface, thus improving the MP emulsification ability and stability. Furthermore, the 9 mT magnetic field-treated MP had the best ability to emulsify oil droplets with a more uniform and smaller emulsion size from 28.593 to 23.443 μm. However, high-intensity magnetic field treatment (12 mT) caused MP particles to aggregate and the hydrophobic binding sites to be buried, which was not conducive to encapsulating oil droplets.

Amorphous carbon modulated-quantum dots NiO for efficient oxygen evolution in anion exchange membrane water electrolyzer

Developing efficient electrocatalysts of elements that are abundant on earth crust is crucial for green hydrogen generation technologies. In particular, the oxygen evolution reaction (OER) under alkaline plays a key role in anion exchange membrane (AEM) electrolyzer to produce green hydrogen but suffers from low kinetic. Herein, nickel oxide quantum dots with highly uniform size distribution on ultrathin amorphous carbon nanosheets (NiO dots/a-carbon) were successfully prepared by a one-step method. Introducing NiO quantum dots onto amorphous carbon modifies the local coordination environment of Ni promoting it into a higher valence state. Benefitting from the promoted Niδ+ (2<δ<3) and the strong connection between Ni and amorphous carbon though Ni-O-C and Ni-C bonds, NiO dots/a-carbon exhibits excellent activity and stability towards OER in 0.1 M KOH using the rotating disk electrode. Moreover, a challenging current density of 500 mA cm−2 is achieved at 1.7 V with a lab-scale AEM electrolyzer.

Preparation of Gypsum–Urea with Enhanced Sustainability from Flue Gas Desulfurization Gypsum in Saturated Urea Solution

Gypsum–urea is a kind of urea product with substantially reduced aqueous solubility and lower hygroscopicity that increases the soil retention time of urea and thus enhance its environmental sustainability. Here, gypsum–urea was prepared using bulk industrial solid waste flue gas desulfurization (FGD) gypsum as a raw material in a saturated urea solution via immobilizing urea molecules into the crystal lattice. The preparation process was achieved through a dissolution–recrystallization mechanism during which FGD gypsum dissolved into Ca2+ and SO42−, which then recrystallized with CO(NH2)2 to form gypsum–urea. The preparation process was almost completed within 10 min, and the formed gypsum–urea presented a uniform size distribution of 30–90 μm and a much lower hygroscopicity and nitrogen release efficiency than that of urea. With a high efficiency of synthesis, and sustainable features, and the recyclability of the saturated mother urea solution, the dissolution–recrystallization-based urea immobilization approach is highly promising regarding the preparation of gypsum–urea with the desired environmental sustainability and contributes to the realization of the sustainable reutilization of FGD gypsum.

Properties and transpiration cooling performance of Cf/SiC porous ceramic composite

Transpiration cooling have gradually become the lead candidate for thermal protection technology of hypersonic vehicle also due to its excellent cooling performance. The porous medium with exceptional properties can further improve thermal protection capability and reliability of transpiration cooling. This paper investigates the preparation and properties of Cf/SiC porous ceramic composite with low density and remarkable permeability, and probes the transpiration cooling performances of ceramic composites (mass ratio of silicon carbide particles and short chopped carbon fibers of 1:1) in the various heat flux conditions. The research results show that Cf/SiC porous ceramic composites prepared by adding short chopped carbon fibers have uniform pore size distributions (3～20 μm) and low densities (1.074 g/cm3 ～ 1.377 g/cm3), as well as outstanding wettability and permeability (6.07 × 10−8 mm2 ～ 12.22 × 10−8 mm2). Besides, The Cf/SiC porous ceramic composites (mass ratio of 1:1) display excellent transpiration cooling performance, meanwhile a new interesting phenomenon that the water pressure difference increases with the rising of heat flow is discovered. Such studies can provide an essential reference for developing porous medium in transpiration cooling technology.

High-speed shearing: An ultra-fast internal energy accumulation method for nucleation of SnZnO in photocatalysis

Zinc oxide (ZnO) nanoparticles and their derivatives, appreciated for their cost-effectiveness, simplicity in synthesis, and versatile applications, have garnered considerable attention. However, unraveling the nucleation and growth mechanisms of ZnO nanoparticles remains a formidable challenge. By comparing the magnetic stirring synthesis (MSS) and high-speed shearing (HSS) methods, we conducted time-dependent calculations of pressure and velocity at various positions in the solution. Under the powerful shearing force, which is the key route to accumulate internal energy (Ein), molecules could achieve at most 174 eV Ein in HSS instead of 0.81 eV Ein in MSS. Molecules could obtain enough energy for nucleation in just 1.03 μs. HSS, utilizing a high-speed rotor for robust shear forces, not only modifies nucleation patterns but also facilitates effective mixing in multi-element systems. SnxZn1−xO1+x nanoparticles prepared through HSS display uniform size, markedly reduced agglomeration, homogeneous element distribution, and a more pronounced bandgap change, causing a decrease in photocatalytic activity to the original 11.2 %.

Performance of High TSS Onion Varieties in Telangana

Field experiments were conducted at Vegetable Research Station, Hyderabad, India during rabi seasons (October–March) of 2019–20, 2020–21 and 2021–22 to study the performance of high TSS varieties of onion in initial evaluation trial, advanced varietal trial-I and advanced varietal trial-II as part of All India Network Research Project on Onion and Garlic. The entries tested were DOGR-HT-1, DOGR-HT-2, DOGR-HT-3, DOGR-HT-4, Agrifound White, PKV White and Bhima Shweta. The predominant colour of all the entries was white and the predominant shape of the bulbs was oval. High amount of uniformity in bulb size was reported by Bhima Shweta and PKV white, while the rest of the entries DOGR-HT-1, 2, 3, 4 and Agrifound White reported average uniformity in bulb size. Among the seven entries tested DOGR-HT-2 reported the highest TSS value (17.77 °Brix) followed by DOGR-HT-3 (15.30 °Brix) and the least TSS value was reported by DOGR-HT-1. Maximum mean bulb weight (100.73 g), marketable yield (49.03 tha-1) and total yield (50.48 t ha-1) was reported by Bhima Shweta and it was followed by PKV White (100.26 g, 48.99 t ha-1 and 50.28 t ha-1). The least average bulb yield (84.31 g), marketable yield (41.09 t ha-1) and total yield (42.34 t ha-1) was reported by DOGR-HT-2 but was at par with DOGR-HT-3 and DOGR-HT-4. Minimum incidence of thrips and purple blotch were noticed in DOGR-HT-4.

Evaluation of immunotoxicity of iron oxide nanoparticles on coelomocytes of Eisenia fetida

Iron oxide nanoparticles (Fe3O4 NPs) have gained considerable attention due to their diverse applications in various fields. However, concerns about their potential toxic effects on the environment and living organisms have also emerged. In this study, we synthesized and characterized Fe3O4 NPs and assessed their immunotoxicity on the coelomocytes of Eisenia fetida. The Fe3O4 NPs were synthesized using a co-precipitation method, and their physicochemical properties were determined using techniques such as X-ray diffraction (XRD), scanning electron microscopy-energy dispersive X-ray (SEM-EDX), transmission electron microscopy (TEM) and Fourier-transform infrared spectroscopy (FTIR). The synthesized Fe3O4 NPs exhibited a uniform size distribution with spherical morphology and the phase purity was confirmed from XRD analysis. To evaluate the immunotoxicity of Fe3O4 NPs, Eisenia fetida coelomocytes were exposed to various concentrations of Fe3O4 NPs for 14 days. Furthermore, we analyzed the impact of Fe3O4 NPs on the biochemical parameters, including superoxide dismutase (SOD), catalase (CAT), acid phosphatase (APs), alkaline phosphatase (ALP), and total protein content (TPC), as well as conducted a histological examination. Biochemical analysis revealed significant alterations in the activity levels of SOD, CAT, APs, ALP, and TPC in the coelomocytes, indicating immune system dysregulation upon exposure to Fe3O4 NPs. Moreover, histological examination demonstrated structural changes, suggesting cellular damage caused by Fe3O4 NPs. These findings provide valuable insights into the immunotoxic effects of Fe3O4 NPs on Eisenia fetida and underscore the need for further investigation into the potential environmental impact of nanoparticles.

Harnessing Aristolochia bracteolate bud extract for green synthesis and characterization of silver nanocomposite films: assessing their potent antimicrobial proficiency

Nanoscience and technology play an essential role in different various scientific fields domains as since it offers unique properties and diverse industrial applications. This study introduces an efficient method to synthesize silver nanoparticles (AgNPs) using Aristolochia bracteolate bud extract. The synthesized AgNPs are embedded within Poly (methyl methacrylate) (PMMA) to prepare a sustainable nanocomposite film (Ag-PMMA NC). Characterization techniques reveal the distinct properties of AgNPs and Ag-PMMA NC. Thermogravimetric analysis (TGA) shows enhanced heat stability of the polymer with Ag nano-filler. UV-vis spectroscopy detects a peak for AgNPs at 440 nm, with an average size of 180.4 nm and a polydispersity index (PDI) of 0.389, indicating uniform size. Fourier transform infrared spectroscopy (FTIR) of Ag-PMMA exhibits characteristic peaks between 300-700 cm-−1, confirming Ag-PMMA interactions. Both green-synthesized AgNPs and the resulting Ag-PMMA NC film demonstrate potent antibacterial activity against Gram-positive Bacillus cereus (∼15 mm) and Gram-negative Escherichia coli (∼26 mm), showing promise for water purification and other applications.

Shell-Core Microbeads Loaded with Probiotics: Influence of Lipid Melting Point on Probiotic Activity.

Probiotics have many beneficial physiological activities, but the poor stability during storage and gastrointestinal digestion limits their application. Therefore, in this study, a novel type of shell-core microbead for loading probiotics was prepared through high-precision concentric drop formation technology using gelatin as the shell material and lipids as the core material. The microbeads have a regular spherical structure, uniform size, low moisture content (<4%) and high probiotic activity (>9.0 log CFU/g). Textural testing showed that the hardness of the medium-chain triglyceride microbeads (MCTBs), cocoa butter replacer microbeads (CBRBs) and hydrogenated palm oil microbeads (HPOBs) increased gradually (319.65, 623.54, 711.41 g), but their springiness decreased (67.7, 43.3, 34.0%). Importantly, lipids with higher melting points contributed to the enhanced stability of probiotics during simulated digestion and storage. The viable probiotic counts of the HCTBs, CBRBs and HPOBs after being stored at 25 °C for 12 months were 8.01, 8.44, and 8.51 log CFU/g, respectively. In the simulated in vitro digestion process, the HPOBs resisted the destructive effects of digestive enzymes and gastric acid on probiotics, with a reduction in the probiotic viability of less than 1.5 log CFU/g. This study can provide new ideas for the preparation of intestinal delivery probiotic foods.

Ionic liquid mediated one-step perpendicular assembly in block copolymer thin films for ultrafiltration membrane applications

The rapid rise of oil and gas, petrochemical, food processing, and pharmaceutical industries has added a complex mixture of contaminants like oil, particulates, metals, and other organic compounds to wastewater. Multipurpose membranes with precise pore structure can offer a solution to this problem and block copolymers (BCP) can be used to achieve such structures. Achieving vertical assembly of BCP domains provides a perfect template for developing uniform through film channels for separation and transport of material, besides being useful for the rectification of defects in photolithography patterns. Producing such morphologies may require extensive film/substrate processing and is not always feasible for scale-up. With this article, we demonstrate a facile solution casting method to induce vertical domain assembly in as-cast diblock copolymer thin films in the presence of an ionic liquid (IL) additive that preferentially segregates to one block and neutralizes interfacial interactions. We also show the tunability of domain sizes by controlling the additive concentration. These vertically aligned morphologies are important for the development of next-generation lithographic techniques and form excellent templates for ultrafiltration membranes with uniform pore sizes. This article demonstrates how IL additives can be used to obtain stable non-equilibrium morphologies in as-cast BCP films and the effect of BCP molecular mass, block volume fractions, and IL content on self-assembly.

A molecular dynamics study on pore structure: Performance comparison between metal foam and artificial mesh porous surface

With the development of surface engineering, porous surfaces have emerged as a significant research subject in boiling heat transfer. The latter, in turn, plays a crucial role in various industries such as power plants, distillation plants, and microelectronic technology. In this paper, the Molecular Dynamics method is adopted to investigate the wicking dynamics and boiling dynamics of two porous surfaces: foam, which exhibits randomly distributed pores, and mesh, composed of ordered square wires with relatively uniform pore sizes. Three wettability, namely hydrophilic, neutral, and hydrophobic wetting states, are assigned to the two porous surfaces de-coupling the effect of wettability from surface structure. Results reveal that, during the wicking process, the foam surface shows better wetting ability as it absorbs liquid under both hydrophilic and neutral wettability. Comparatively, the mesh surface has the fastest wicking speed under hydrophilic wettability yet it becomes non-wetting under neutral wettability. During the boiling process, the boiling dynamics differ greatly under three wettability. More importantly, the difference in surface structure makes the foam surface possess a better heat transfer whereas the mesh surface causes gentle pressure variation. Our findings provide insights into the design of artificial porous surfaces for certain purpose and their potential application.

Hierarchical Silica Composites for Enhanced Water Adsorption at Low Humidity.

To combat water scarcity in remote areas around the world, adsorption-based atmospheric water harvesting (AWH) has been proposed as a technology that can be used alongside existing water production capabilities. However, commonly used adsorbents either have low water adsorption loadings or are difficult to regenerate. In this work, we developed two novel hierarchical silica-salt composites that both exhibit high water adsorption loadings under dry and humid conditions. The total water vapor loading, kinetics, and heats of water adsorption for both silica-salt composites were investigated. As hierarchical silicas have tunable pores and large pore volumes, these materials serve as effective host matrixes for the hygroscopic salt LiCl. Our results suggest that hierarchical pores play a significant role in water adsorption: micropores and some smaller mesopores act as "storage" sites for hygroscopic salt, whereas larger mesopores and macropores increase the accessibility of water vapor into the silica. Using this mix of pores, we achieved greater than 0.4 g H2O/g composite at 10% RH and 27 °C. Additionally, we found that the salt-impregnated silica and bare silica had the same heat of adsorption: 80-90 kJ/mol. The results suggest that the H-bond interactions are similar for both systems and that the primary mechanism at play here is water cluster adsorption/desorption. Despite the similar energies, the LiCl-containing materials exhibited considerably slower kinetics than bare silica materials. Of equal importance to the adsorption capacity and kinetics of these composites is their mechanical stability. To assess their mechanical stability, high-energy ball milling of silica was conducted to create more uniform particle sizes. However, reduced particle sizes came at a cost─the BET surface areas and pore volumes were drastically decreased after more than 1 h of ball milling. Findings from this study suggest that short-term ball milling may be a viable large-scale option to reduce particle size in silica materials without sacrificing significant performance.

Biosynthesized gold nanoparticles for enhanced determination of nicotine in heated tobacco products

An electrochemical sensor for nicotine determination in heated tobacco products (HTPs) was developed using biosynthesized AuNPs from Ceiba pentandra leaf extract. The biosynthesis process was optimized by investigating the effects of HauCl4 concentration, extract volume, reaction temperature, and time on the formation of gold nanoparticles (AuNPs). The biosynthesized AuNPs were characterized using various techniques, confirming their crystallinity, spherical morphology, and uniform size distribution with an average diameter of 19.8 ± 3.6 nm. The AuNP modified glassy carbon electrode (AuNP/GCE) exhibited enhanced electrochemical performance compared to the bare GCE, facilitating efficient oxidation of nicotine. The AuNP/GCE sensor demonstrated a wide linear range of 0.02–280 µmol L−1 and a low limit of detection of 0.01 µmol L−1 for nicotine determination. The sensor showed excellent selectivity towards nicotine in the presence of common interfering substances, with negligible responses (<5 % change) to uric acid, paracetamol, glucose, melamine, L-cysteine, and dopamine. The AuNP/GCE sensor's applicability was validated by analyzing nicotine levels in real HTP samples, with excellent recovery rates (97.6–102.4 %) and good agreement with the HPLC (R2 = 0.998). The biosynthesized AuNP-based electrochemical sensor offers a rapid, sensitive, eco-friendly, and cost-effective approach for nicotine determination in HTPs, providing a valuable tool for quality control and regulatory purposes.