Scanning Atomic Force Microscopy Research Articles

Effect of Sintering Temperature on Ceramic Membrane Fabricated Using Coal Flyash and Natural Clay for Lignin Recovery

This study explores the utilization of coal fly ash combined with natural clay as a precursor for creating ceramic membranes through the uniaxial compaction method, aiming at lignin separation. These membranes were sintered at varying temperatures from 600 to 1000 °C. Thermal Gravimetric Analysis (TGA) revealed the robust thermal stability of the membranes. Fourier Transform Infrared (FTIR) analysis affirmed the presence of silica and alumina within the membranes. X-ray Diffraction (XRD) peaks indicated the crystalline structure and the presence of metal oxides originating from the fly ash and clay components. Scanning Electron Microscopy (SEM) and Atomic Force Microscopy (AFM) images illustrated the porous nature and rough surface of the ceramic membranes. The average pore radius of the fabricated membrane expanded from 43.12 to 7.91 nm with increasing temperature. Concurrently, membrane flux decreased from 4.13 to 0.96 ×10-6 m3/m2 s with higher temperatures. Lower contact angles indicated the hydrophilic properties of membranes. All membranes exhibited superior corrosion resistance and negative zeta potential, owing to the significant silica content in the fly ash. Lignin separation efficiency increased from 65 % to 81 % with increasing temperatures. The optimal sintering temperature was determined to be 800 °C, achieving a lignin recovery greater than 76 % and a membrane permeability of about 7×10-9 m3/m2 s kPa. Thus, the fly ash-clay-based ultrafiltration membranes synthesized in this study offer the potential for lignin biomass recovery from biorefinery effluent.

The effect of whitening toothpastes on the color stability and surface roughness of stained resin composite

BackgroundThis study aimed to investigate the effect of whitening toothpastes on the color stability and surface roughness of resin composites stained with coffee and cigarette smoke.MethodsSeventy-two disk-shaped specimens (6 × 2 mm) of suprananohybrid resin composite were randomly divided into two groups and exposed to coffee and cigarette smoke (n = 36). After staining, the samples randomly divided into four groups according to whitening toothpastes and were brushed for 4 min: Opalescence Whitening (OW); Colgate Optic White (COW); Curaprox Black is White (CPX) and, distilled water (control) (n = 9). Color was measured with spectrophotometer at the initial, after staining, and after brushing, and surface roughness was measured with profilometer at the initial and after brushing. A surface morphology analysis was examined using scanning electron microscopy and atomic force microscopy. The obtained data were statistically analyzed. (p < 0.05).ResultsCigarette smoke caused a significantly higher color change than coffee in the resin composite (p < 0.05). Brushing with hydrogen peroxide and silica-containing whitening toothpaste showed significant differences in color change (p < 0.05). The lowest whitening effect was found in activated charcoal-containing toothpaste. While all toothpastes increased the degree of surface roughness of resin composites, the highest roughness was caused by whitening toothpastes containing activated charcoal. (p < 0.05).ConclusionsThe color stability and surface properties of resin composites can be affected by brushing them with whitening toothpaste. The utilization of whitening toothpaste containing hydrogen peroxide can be considered a safe method for increasing the whiteness of discolored resin composites.

A Comparative Analysis of Enamel Surface Roughness Following Various Interproximal Reduction Techniques: An Examination Using Scanning Electron Microscopy and Atomic Force Microscopy

Interproximal enamel reduction (IER) is a minimally invasive therapeutic procedure commonly used in orthodontics to address both functional and aesthetic issues. Its mechanical effects on enamel surfaces induce the formation of grooves, furrows, scratches, depressions, and valleys. The aim of this study was to assess the enamel surface roughness resulting after the application of currently available methods for interproximal reduction. Ninety freshly extracted human teeth were divided into six groups and subjected to the stripping procedure, using a different method for each group (diamond burs, abrasive strips of 90 μm, 60 μm, 40 μm, 15 μm, and abrasive discs). A single individual performed stripping according to the manufacturer’s recommendations, involving interproximal reduction on one tooth’s proximal face and leaving the other side untreated. Qualitative and quantitative assessment of the enamel surfaces was carried out using Scanning Electron Microscopy (SEM) and Atomic Force Microscopy (AFM), obtaining 2D and volumetric 3D images of the enamel surface microstructure and nanostructure. The study found that diamond burs and abrasive strips of 60 μm and 90 μm increased enamel roughness due to intense de-structuring effects, while the 40 μm polisher had a gentler effect and 15 μm abrasive strips and polishing discs preserved enamel surface quality and removed natural wear traces.

Characterization and mechanism analysis of interfacial shear strength between individual aramid fiber and epoxy by oxygen plasma treatment at elevated temperatures: Experiment and simulation

The weak adhesion between aramid fibers Ⅲ and the resin matrix, due to its smooth surface and high inertness of the fibers. This property restricts the mechanical properties of the composites in high temperatures environments. This work describes the treatment of aramid fibers Ⅲ with oxygen plasma to introduce reactive oxygen-containing functional groups onto fiber surface. The analysis focused on the impact of interfacial friction and interfacial wettability on the transfer of load across composites at various temperatures. According to the X-ray photoelectron spectroscopy (XPS) analysis, the fiber surface showed an increase in the number of active groups after plasma treatment. In addition, two new oxygen-containing functional groups -C-O- and -O-CO appeared. The use of Scanning Electron Microscopy (SEM) and atomic Force Microscopy (AFM) showed that the plasma treatment has an etching effect on the fiber surface and increases the roughness of the fiber surface. Furthermore, after plasma treatment, the fibers adhered to the resin matrix through hydrogen bonding and π-π bonding. The utilization of this technique led to a significant enhancement in the interfacial properties of monofilament composites across various temperature ranges. The IFSS of plasma-treated aramid fiber Ⅲ/EP exhibited increases of 38 % at the test temperature of 25℃. Surprisingly, the IFSS of plasma-treated aramid fiber III/EP exhibited a significant increase of 52 % at the test temperature of 120℃. In this paper, COMSOL software was utilized to simulate the IFSS before and after plasma treatment at different temperatures. Mechanistically explains the effect of temperature on the interfacial mechanical properties of composites.

Microstructure and optical properties of Au:N doped diamond-like carbon films: Effect of working pressure

In recent years, the incorporation of impurities (metallic or non-metallic) into diamond-like carbon films for industrial and biological applications has garnered considerable attention from researchers. In this study, gold nanoparticles and nitrogen impurities were introduced into diamond-like carbon using a co-deposition method involving Radio Frequency Plasma-Enhanced Chemical Vapor Deposition (RF-PECVD) and Radio Frequency Sputtering (RF-sputtering),modifying the working pressure from 14.5 to 19.5 mTorr. X-ray Diffraction (XRD) patterns confirmed the presence of gold nanocrystals in the samples. The surface morphology of the films was analyzed using images obtained from Scanning Electron Microscopy (SEM) and Atomic Force Microscopy (AFM) subjected to statistical and fractal analyses. These investigations revealed non-symmetric Gaussian distributions of the grains, demonstrating a multifractal nature in all samples, as well as a complex relationship between film roughness and working pressure. Films prepared at working pressures of 16.5 and 18.5 mTorr exhibited the roughest and smoothest surfaces, respectively. Fast Fourier Infrared (FTIR) spectroscopy was used to identify functional groups and to estimate the sp2/sp3 ratio. Raman spectra show D and G bands associated with the disordered graphitic carbon of the DLC, with the intensity of the G band being higher than that of the D band, indicating a higher sp2 bonding content compared to sp3 bonding. Subsequently, the absorption UV–visible spectrum of the samples was examined, confirming the presence of gold nanoparticles in the films, as evidenced by the occurrence of a Localized Surface Plasmon Resonance peak, whose location dependent on the working pressure used during deposition. These observations are consistent with other microscopic and structural analyses.

A novel refractive index based-fiber optic sensor for milk adulteration detection

Milk adulteration poses a significant risk to public health and consumer trust, compromising its nutritional value. To address this, we've developed an optical fiber-based sensor using a Lossy Mode Resonance (LMR) approach. Antimony Oxide (Sb2O3) serves as the sensing layer, deposited onto the optical fiber's unclad core using Radio Frequency Magnetron sputtering. The sensing layer underwent comprehensive characterization, including X-Ray diffraction (XRD), UV–Vis spectroscopy, Ellipsometer, Atomic Force Microscopy (AFM), EDAX, and Field Emission Scanning Microscopy (FESEM). The sensor was tested for formaldehyde and water adulteration across normal milk type 1, full-fat milk type 2, vendor milk type 3, and, with concentrations ranging from 0 % to 10 %. Observations included resonance wavelength shifts and sensing parameters such as sensor response, sensitivity, and repeatability. For Sb2O3-coated sensor probes, responses to formaldehyde and water adulteration for type 1 milk is 2.05 % and 2.22 %, type 2 milk is 2.17 % and 2.4 %, and type 3 milk is 1.90 % and 1.95 %. Sensitivity for Sb2O3-coated probe to formaldehyde are 2.2 nm/v% (type 1 milk),1.9 nm/v% (type 2 milk) and 1.5 nm/v% (type 3 milk). For water in milk, the sensitivities are 1.7 nm/v%, 1.5 nm/v%, and 1.2 nm/v%. Furthermore, a prototype sensor probe has been developed for continuous milk adulteration monitoring, interfaced with Arduino and Thing Speak.

Conversion of preferred crystalline orientation by annealing and its impacts on the structural, electronic, and optical properties of pulsed laser-deposited CdO thin films

The impact of annealing on the preferred crystalline orientation as well as the structural, electronic, and optical properties of pulsed laser-deposited 150 ± 3 nm thick cadmium oxide (CdO) films was studied. X-ray diffraction analysis revealed that the annealed CdO films have smaller crystallite sizes, as their molecules at the grain boundaries possessed enough kinetic energy to rearrange their preferred crystalline orientation between (111) and (200). The atomic force microscopy and field emission scanning electron microscopy analyses revealed an enhancement in the active surface area with optimized grain boundaries by annealing which facilitates gas adsorption/desorption. DC electrical conductivity depends on the annealing process and reveals two different conduction mechanisms. The direct optical energy gap was decreased from 3.41 eV to 2.76 eV by annealing at 473 K which is greater than the theoretical value, i.e. 2.2 eV, for bulk CdO. The findings agree with the Burstein-Moss effect as a result of the increased carrier concentration following the generation of numerous oxygen vacancy sites and Cd interstitials. However, mutual charge carrier-impurity interaction and charge carrier Columb interaction contributed to narrowing the band gap by increasing the annealing temperature. The enhanced values of Urbach energy, optical packing density, dispersion parameters, optical conductivity, dissipation factor, oscillator strength, and lattice dielectric constant supported the effectiveness of the annealing process on tailoring optoelectronic responses in the infrared region for the CdO thin films for use in optoelectronic devices. Moreover, the calculated linear optical susceptibility, and nonlinear constants (i.e. third-order optical susceptibility and nonlinear refractive index) were the highest for CdO films annealed at 473 K. The improved value of the figure of merit, solar material protection factor, and solar skin protection factor for the CdO films, annealed at 473 K supports its use in several photovoltaic applications, including solar cells.

Extraction and Structural Analysis of Sweet Potato Pectin and Characterization of Its Gel.

Pectin is widely used in the food and pharmaceutical industries. However, data on sweet potato pectin extraction and structural property analyses are lacking. Here, for the high-value utilization of agricultural processing waste, sweet potato residue, a byproduct of sweet potato starch processing, was used as raw material. Ammonium oxalate, trisodium citrate, disodium hydrogen phosphate, hydrochloric acid and citric acid were used as extractants for the pectin constituents, among which ammonium oxalate had a high extraction rate of sweet potato pectin, low ash content and high molecular weight. Structural and gelation analyses were conducted on ammonium oxalate-extracted purified sweet potato pectin (AMOP). Analyses showed that AMOP is a rhamnogalacturonan-I-type pectin, with a molecular weight of 192.5 kg/mol. Chemical titration and infrared spectroscopy analysis confirmed that AMOP is a low-ester pectin, and scanning electron and atomic force microscopy demonstrated its linear molecular structure. Gelation studies have revealed that Ca2+ is the key factor for gel formation, and that sucrose significantly enhanced gel hardness. The highest AMOP gel hardness was observed at pH 4, with a Ca2+ concentration of 30 mg/g, pectin concentration of 2%, and sucrose concentration of 40%, reaching 128.87 g. These results provide a foundation for sweet potato pectin production and applications.

Application of Recycled Ultrafiltration Membranes in an Aerobic Membrane Bioreactor (aMBR): A Validation Study.

A validation study using recycled ultrafiltration membranes (r-UF) on an aerobic membrane bioreactor (aMBR) was conducted for the first time. Four different polyethersulfone (PES) membranes were tested using synthetic urban wastewater (COD 0.4-0.5 g/L) during two experimental periods: (i) recycled ultrafiltration membrane (r-UF) and commercial UF membrane (molecular weight cut-off (MWCO) 150 kDa) (c-150 kDa); (ii) r-UF membrane modified by dip-coating using catechol (CA) and polyethyleneimine (PEI) (mr-UF) and c-20 kDa membrane. Permeability, fouling behavior, and permeate quality were evaluated. Extensive membrane characterization was conducted using scanning electron microscopy (SEM), atomic force microscopy (AFM), energy-dispersive X-ray (EDX), and confocal laser scanning microscopy (CLSM). Permeate quality for r-UF and mr-UF membranes was excellent and comparable to that obtained using commercial membranes under similar conditions. Additionally, r-UF and mr-UF membranes presented a steadier performance time. Additionally, r-UF membrane demonstrated less tendency to be fouled (Rf, m-1) r-UF 7.92 ± 0.57 × 1012; mr-UF 9.90 ± 0.14 × 1012, c-150 kDa 1.56 ± 0.07 × 1013 and c-20 kDa 1.25 ± 0.50 × 1013. The r-UF membrane showed an excellent antibiofouling character. Therefore, r-UF membranes can be successfully implemented for wastewater treatment in aMBR, being a sustainable and cost-effective alternative to commercial membranes that can contribute to overcome membrane fouling and membrane replacement issues.

Simple and Rapid Monolayer Self-Assembly of Nanoparticles at the Air/Water Interface.

Colloidal crystals and their two-dimensional (2D) monolayers, which have been commonly applied in nanosphere lithography, have the potential to revolutionize many engineering disciplines; however, current production techniques are hampered by a restricted preparation area, laborious procedures, and the need for advanced equipment. We propose a self-assembly-driven, simple, and low-cost method to prepare 2D colloidal nanosphere monolayers with excellent repeatability across wide regions. The self-assembly capability of colloidal polystyrene (PS) nanospheres at the air/water interface was utilized to transfer the assembled monolayers onto a substrate. This innovative method combines the advantages of methods that permit deposition at the air/water interface, such as Langmuir and drop coating, in order to deliver defect-free, simple-to-install, and simple-to-apply deposition across vast regions. Using field emission scanning electron microscopy and atomic force microscopy, the resultant coatings were characterized. The size of the nanospheres was reduced using an oxygen plasma etch process in an inductively coupled plasma reactive ion etching system, and the reflectance properties of the substrates for various nanosphere sizes were investigated. By evaporation of a thin gold capping layer on the templates, their optical properties were compared using surface-enhanced Raman scattering spectroscopy. This work has the potential to expand the use of nanosphere lithography by offering a simple and reproducible method that eliminates the need for complicated experimental setups and reduces the amount of material required for monolayer coating, thus lowering the cost.

Temperature dependence of the friction and wear behavior of pure tungsten

In this work, the friction and wear characteristics of rolled pure tungsten were investigated by using atomic force microscope (AFM) and field emission scanning electron microscope (SEM) with electron backscatter diffraction (EBSD) characterization techniques. A ductile to brittle transition (DBT) related frictional wear behaviors have been discovered. The results indicated that the coefficient of friction maintains an almost constant value of 0.45 at low temperatures (≤ 400 °C), whereas it consistently decreases at 600 °C due to the generation of a surface oxide. The wear rate varies with temperatures and reaches a maximum at 200 °C due to the transition of the tungsten matrix from brittleness to pseudoplasticity, which leads to severe adhesive wear and large mass loss. In addition, the evolution of sub-grains underneath the friction layer and Vickers microhardness were evaluated as well. This work provides insight into understanding the relationship between temperatures, microstructure and the frictional properties of tungsten materials, and thus provides guidance for improving frictional wear behaviors in tungsten materials.

Mechanistic insight into the Janus Green B on electrochemical roughening layer of copper foil

This study explores the impact of the electroplating additive JGB the surface characteristics and peel strength of electrolytic copper foils used in printed circuit boards. Utilizing Scanning Electron Microscopy and Atomic Force Microscopy, we found that optimal JGB concentrations enhance the morphology and roughness of the copper foil roughening layer while maintaining high peel strength. The ideal concentration of 3 mg/L achieved an average roughness of 0.953 µm and a peel strength of 0.946 N/mm. JGB's effectiveness in inhibiting copper deposition was confirmed through cyclic voltammetry, linear sweep voltammetry, and electrochemical impedance spectroscopy. Density Functional Theory calculations and in situ infrared spectroscopy elucidated JGB's adsorption and coordination actions, which have a synergistic effect on its inhibitory performance. Further investigations with molecular dynamics simulations and finite element analysis demonstrated JGB's preferential adsorption in areas of high electric field intensity, effectively controlling the copper grain morphology in the roughening layer. This research highlights the potential of dye-type additives in improving copper foil roughening for printed circuit boards applications. Future research should explore the long-term stability and environmental impact of JGB in industrial applications, while investigating other dye-type additives may further optimize the roughening process to meet diverse printed circuit boards manufacturing needs.

Erosive wear and topographical study of zinc-aluminum based composite reinforced with in-situ formed ZrB2 particles

The present study deals with the erosive wear behaviour of a zinc-aluminum (ZA) alloy and composite in the slurry medium. The effects of reinforcement of zirconium diboride (ZrB2) particles in ZA alloy, as well as the impingement angle and duration of erosion wear responses have been studied. The slurry composition was prepared with 1.5 L of water and 500 g silica of a size range of 350–450 μm. The erosion tests are performed at a speed of 600 rpm for varying durations (20–80 h) and impingement angles (30°–90°). The erosive wear responses of the samples have been analyzed in terms of distinct features of their micro constituents like ZrB2 and the material removal mechanism in a prescribed set of conditions. A significant decrease in composite erosion compared to ZA alloy has been observed. With increased duration, both alloy and composite show increased erosive wear. Obtained results revealed that the composite shows 60–80 % less erosive wear than ZA alloy on operating conditions. The optimum results in wear have been observed at 45° for alloy and 60° for composite. Investigating topographical aspects using scanning electron microscopy and atomic force microscopy revealed that ZrB2 reinforcements resulted in smoother topography and reduced erosive wear.

Large Area Film of Highly Crystalline, Cleavable, and Transferable Semi-Conducting 2D-Imine Covalent Organic Framework on Dielectric Glass Substrate.

Two dimensional (2D) imine-based covalent organic framework (COF), 2D-COF, is a newly emerging molecular 2D polymer with potential applications in thin film electronics, sensing, and catalysis. It is considered an ideal candidate due to its robust 2D nature and precise tunability of the electronic and functional properties. Herein, we report a scalable facile synthesis of 2D imine-COF with control over film thickness (ranging from 100 nm to a few monolayers) and film dimension reaching up to 2 cm on a dielectric (glass) substrate. Highly crystalline 2D imine polymer films are formed by maintaining a quasi-equilibrium (very slow, ∼15 h) in Schiff base condensation reaction between p-phenylenediamine (PDA) and benzene-1,3,5-tricarboxaldehyde (TCA) molecules. Free-standing thin and ultrathin films of imine-COF are obtained using sonication exfoliation of 2D-COF polymer. Insights into the microstructure of thin/ultrathin imine-COF are obtained using scanning and transmission electron microscopy (SEM and TEM) and atomic force microscopy (AFM), which shows high crystallinity and 2D layered structure in both thin and ultrathin films. The chemical nature of the 2D polymer was established using X-ray photoelectron spectroscopy (XPS). Optical band gap measurements also reveal a semiconducting gap. This is further established by electronic structure calculation using density functional theory (DFT), which reveals a semiconductor-like band structure with strong dispersion in bands near conduction and valence band edges. The structural characteristics (layered morphology and microscopic structure) of 2D imine-COF show significant potential for its application in thin film device fabrication. In addition, the electronic structure shows strong dispersion in the frontier bands, making it a potential semiconducting material for charge carrier transportation in electronic devices.

Konjac glucomannan/xanthan synergistic interaction gel: Effect of the fine structure of xanthan on enthalpy driven assembly behavior and gel strength

Understanding the intricate relationships between the fine structure of xanthan on the assembly of konjac glucomannan (KGM) and xanthan is crucial for developing KGM/xanthan synergistic interaction gels. A combination of micro-differential scanning calorimetry, rheometry and atomic force microscopy were employed to explore the assembly process of KGM and xanthan with varying fine structures. Xanthan possessing standard acetyl (4.57%) and high pyruvate group contents (6.49%)(SA/HP) exhibited type-A and type-B bindings when interacting with KGM through cooling process. Decreasing these group contents effectively reduced type-B binding. Additionally, removal of pyruvate groups to 5.53% amplified type-A binding and gel strength from 258 Pa to 653 Pa, thanks to the improved helical structure forming ability of xanthan. Decreasing acetyl groups also intensified type-A interaction and gel strength from 258 Pa to 872 Pa. This stemmed from the formation of more stable assembly structure of xanthan and KGM, compared to the helical structure of deacetylated xanthan. These findings hold promise for the rational design of KGM/xanthan systems for versatile applications.

Atomic force microscopy monitoring of subcritical slow crack growth in soda lime silicate glass

Prediction of brittle fracture in silicate glasses requires a fundamental understanding of slow crack growth rates, far below the critical stress intensity (KIC) of the material. Here, atomic force microscopy (AFM) was used to characterize slow crack propagation in soda lime silicate glasses. Using large-sample AFM systems with specialized tips and scanners, fractures less than 20 nm wide were measured as a function of relative humidity (RH). The results were found to be sensitive to the type of AFM tip used and to the dryness of the surface. Continuous scanning and image capture over several days allowed the determination of the crack tip velocity. The dependance of crack tip velocity on RH was measured by enclosing the sample and AFM head in a humidity-controlled chamber. The crack tip velocity was measured as low 4.0×10-12 m/s at 15 % RH and as high as 3.7×10-10 m/s at 40 % RH. Overall crack growth was smooth during the AFM scan. Additionally, recession of the crack tip was noted as the sample dried, indicating crack tip closure may be occurring. Further studies on alternative compositions will provide details on subcritical fracture processes in a range of different environmental conditions.

Therapeutic cargo-free linalool-based nanoparticles attenuate inflammation by targeting NLRP3 inflammasome

Linalool is a commonly used monoterpene obtained from the essential oils of plants that impart multiple pharmacological effects. However, because of poor aqueous solubility, therapeutic efficacy is low, therefore effective methods are desired for improving the efficacy of linalool. In this study, instead of encapsulating linalool, we directly amalgamated linalool with glyceryl monostearate (GMS) and formulate linalool-based nanoparticles (Lin-NPs) using the hot melt method. Subsequently, we characterized Lin-NPs for targeting and suppressing the lipopolysaccharide (LPS)-induced inflammation in RAW264.7 cells. The hydrodynamic diameter of GMS-NPs was ∼175 nm but after amalgamating with linalool, the hydrodynamic diameter was found to be ∼214 nm. Furthermore, particle size and surface morphological characteristics were further confirmed with scanning electron microscopy and atomic force microscopy. The formulation of Lin-NPs was also demonstrated with Fourier-transform infrared spectroscopy (FTIR). These Lin-NPs were then assessed for their pharmacological efficacy in terms of their anti-inflammatory potential. These Lin-NPs effectively suppressed the ROS generation. Finally, investigated the effects of Lin-NPs on the NLRP3 inflammasome pathway as confirmed by the inhibition of NLRP-3, caspase-1 (inhibition of the inflammatory response initiator), and significant suppression of the other downstream biomarkers of the NLRP3 inflammasome pathway such as interleukin-1β and interleukin-18. In conclusion, amalgamation of linalool in GMS to develop Lin-NPs improved the efficacy of linalool, and plausible anti-inflammatory effects of Lin-NPs might be due to inhibition of NLRP3 inflammasome pathway. Moreover, the GMS and linalool both are listed under the FDA-approved Generally Recognized as Safe (GRAS) material and therefore Lin-NPs could supplement as potential NPs to combat inflammation.

Effect of high sodium ion level on the interaction of AmB with a cholesterol-rich phospholipid monolayer.

Invasive fungal infections are a primary reason for high mortality in immunocompromised people, especially in critically ill patients, such as intensive care unit (ICU) patients, advanced cancer patients, or severe burn patients. Hypernatremia also can increase mortality in severely ill patients. Amphotericin B (AmB) is the gold standard for treating infections, but in severely ill patients, AmB can cause hematotoxicity when administered intravenously due to its interaction with cholesterol on red blood cell membranes. This results in limited doses of AmB and affects the treatment of infections. The proportion of cholesterol molecules in membrane lipids in red blood cells is as high as 50mol%, and the sodium ions can influence the interaction between AmB and lipids on the membrane. Therefore, in the complex clinical situation of a severely ill patient with a fungal infection and hypernatremia, the interaction between amphotericin B and the red blood cell membranes is worth studying in depth. In this work, the interaction between AmB and the dipalmitoyl phosphatidylcholine (DPPC)/cholesterol mixed monolayer in the presence of high sodium ion levels was studied when the proportion of cholesterol was 50%. The results show that the effect of AmB on reducing the monolayer's area at a high level of sodium ions is slightly stronger at 30mN/m. The effect of AmB on reducing the elastic modulus of the DPPC/Chol monolayer is significantly weakened by a high sodium ion level, compared with the level of sodium ions at normal physiological concentration. The higher the sodium ion concentration, the weaker the intermolecular force of the DPPC/Chol/AmB mixed monolayers. The scanning electron microscope (SEM) and atomic force microscopy (AFM) observations suggest that at a high sodium ion level, the presence of AmB significantly reduces the surface roughness of the DPPC/Chol monolayer. AmB may bind to cholesterol molecules, and it isolates cholesterol from the monolayer, resulting in a reduced height of the cholesterol-rich monolayer and an increasingly dispersed monolayer region. The results are beneficial to understanding the mechanism of impact of a high sodium ion level on the relationship between AmB and red blood cell membranes rich in cholesterol and are valuable for understanding the hemolytic toxicity of AmB to red blood cells at a high sodium ion level.

Synthesis and characterization of a new eco-friendly dopamine derivative schiff base as an effective corrosion inhibitor for mild steel in acidic environment

The natural corrosion inhibitor behaviour of a newly synthesized dopamine derivative Schiff base (4-DBAB) has been inspected on mild steel in aggressive 1 M HCl using linear polarization, electrochemical impedance spectroscopy and potentiodynamic polarization techniques. The Schiff base was synthesized by eco-friendly pathway. Characterization of the synthesized new non-toxic inhibitor was performed using FT-IR and 1H-NMR spectroscopy techniques. The anti-corrosive efficiencies at optimum concentration of 4-DBAB inhibitor was 87.4% after 1 h and 98.4% after 120 h by impedance technique in acidic solution. The potential of zero charge of mild steel was also determined to elucidate the inhibition mechanism in the presence of the highest 4-DBAB solution. The atomic force microscopy and field emission scanning electron microscopy researches performed on surface morphology to provide additional support on the interaction between the mild steel surface and 4-DBAB molecules. Adsorption behaviour of the inhibitor was also studied at different durations by experimental inhibition results and showed the Langmuir isotherm involving chemisorption. Highlights A new dopamine-derived Schiff base (4-DBAB) with natural and environmentally friendly corrosion inhibition properties was synthesized. (Synthesis of eco-friendly compound). 4-DBAB demonstrated a high anti-corrosive efficiency after 120 hours in aggressive 1M HCl, as determined by impedance technique. (Exceptional corrosion inhibition). The determination of the potential of zero charge of mild steel provided insights into the inhibition mechanism in the presence of the highest 4-DBAB solution. (Mechanism elucidation). AFM and FE-SEM studies on surface morphology supported the interaction between the mild steel and 4-DBAB molecules, affirming its corrosion inhibition properties. (Surface interaction analysis).

The effect of nanobubbles on Langmuir-Blodgett films

Nanobubbles (NBs) are classified in two distinct categories: surface and bulk. Surface NBs are readily observed using atomic force microscopy (AFM), while the existence of bulk NBs has been a subject of debate, conflicting with the diffusion theory's predictions. Current methodologies for identifying bulk NBs yield inconclusive results. In this study, Langmuir Blodgett (LB) technique and AFM, are utilized to visualize NB imprints on anionic, cationic and zwitterionic lipid films deposited on glass-slide substrates. Our analysis of Langmuir monolayers compression isotherms reveals the impact of bulk NBs on lipid monolayer development. AFM scans of the deposited lipid films consistently show NB imprints. Notably, cationic and zwitterionic film depositions exhibit NB formations from the 1st layer, whereas in anionic films, these formations are observed only after the 3rd layer. These results suggest that the origin of these imprinted formations may be attributed to bulk NBs.