Scanning Electron Microscopy Observations Research Articles

Fabrication and electrochemical properties of Mn, N, and S co-doped carbon fiber composite bamboo-based woodceramics electrodes

Prepared in this study, Mn, N and S co-doped woodceramics electrodes (WC@Mn-N/S) were prepared using waste bamboo as the base material, carbon fiber as the reinforcement fiber, KMnO4 and CH4N2S as dopants and activators. Mechanical analysis revealed a 68 % increase in the flexural strength of the matrix material reinforced with carbon fibers. Scanning electron microscopy observation indicated that WC@Mn-N/S retained the original natural pore structure of bamboo. The specific surface area (BET) analysis revealed that WC@Mn-N/S exhibited a specific surface area of 861.7 m2/g, with its pore size structure mainly distributed in the range of 1.3–3.8 nm. Electrochemical performance tests showed that the introduction of Mn, N and S elements endowed the bamboo-based electrode with pseudocapacitance characteristics. Additionally, the synergistic effect between these three elements imparted pseudocapacitance to the electrode material. WC@Mn-N/S performent a specific capacitance of 615 F/g, at 0.2 A/g with excellent capacitance retention (99.4 % after 5000 cycles). In the practical assembled in symmetrical capacitor the material showed high power density 500 W/kg and energy density 57.9 Wh/kg, indicating its excellent electrochemical performance.

Gold nanosheet modified electrode with reduced impedance for electrophysiological recordings

In neurophysiological recording, reducing electrode impedance is crucial for enhancing the signal-to-noise ratio and achieving the desired spatial resolution. This study presents an approach to improve the performance of Au/Cr/glass electrodes by incorporating synthesized gold nanosheets without the need for additional adhesive material. We characterized the performance of the modified electrodes using electrochemical impedance spectroscopy and equivalent circuit analysis. Our findings showed an 81% reduction in mean impedance for the modified electrode, which was 0.85 kΩ at 1 kHz, compared to the unmodified electrode at 4.5 kΩ, an improvement attributed to the higher effective surface area of the modified electrode. Additionally, Scanning electron microscopy observations of PC12 cells cultured on the modified electrodes indicated favorable cell elongation and interaction with the rough surface. Stability studies indicated acceptable performance of the modified electrodes in solution environments. These results suggest that surface modification of electrodes with gold nanosheets could be a promising strategy for enhancing neural interface applications.

Preparation of Polyoxymethylene/Exfoliated Molybdenum Disulfide Nanocomposite through Solid-State Shear Milling.

In this paper, the solid-state shear milling (S3M) strategy featuring a very strong three-dimensional shear stress field was adopted to prepare the high-performance polyoxymethylene (POM)/molybdenum disulfide (MoS2) functional nanocomposite. The transmission electron microscope and Raman measurement results confirmed that the bulk MoS2 particle was successfully exfoliated into few-layer MoS2 nanoplatelets by the above simple S3M physical method. The polarized optical microscope (PLM) observation indicated the pan-milled nanoscale MoS2 particles presented a better dispersion performance in the POM matrix. The results of the tribological test indicated that the incorporation of MoS2 could substantially improve the wear resistance performance of POM. Moreover, the pan-milled exfoliated MoS2 nanosheets could further substantially decrease the friction coefficient of POM. Scanning electron microscope observations on the worn scar revealed the tribological mechanism of the POM/MoS2 nanocomposite prepared by solid-state shear milling. The tensile test results showed that the pan-milled POM/MoS2 nanocomposite has much higher elongation at break than the conventionally melt-compounded material. The solid-state shear milling strategy shows a promising prospect in the preparation of functional nanocomposite with excellent comprehensive performance at a large scale.

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.

Effect of bismuth doping on electrodeposition, physicochemical properties and electrocatalytic activity of lead dioxide electrodes

The bismuth (Bi)-doped PbO2 electrodes were electrodeposited from a nitric plating solution containing Pb (II) and Bi (III) ions by varying the concentrations of Bi (III). Cyclic voltammetry was used to investigate the effect of Bi (III) ions on the kinetics of PbO2 electrodeposition. It is observed that increasing Bi (III) ions in the plating solution reduces the rate of nucleation or formation of PbO2 but does not change the process mechanism. X-ray diffraction confirms that the incorporation of bismuth results in an apparent β (301) texture. Scanning electron microscopic observation reveals that the size of the PbO2-deposit particles gradually decreases by several micrometers as the doping content of Bi (III) increases from 2 to 6 mM. Linear scanning voltammograms show that the oxygen overpotential on Bi-PbO2 is much higher than on undoped PbO2 electrodes. Electrochemical degradation of the target pollutant was performed, and HPLC analysis demonstrated that Bi doping significantly improves the electrocatalytic ability of PbO2 electrodes.

Flaw sensitivity of bacterial cellulose hydrogel under monotonic and cyclic loadings

The presence of flaw in solid materials can lead to stress concentration, resulting in the reduction of rupture stress and stretchability of material. When the flaw is sufficiently smaller than a material-specific length, referred to as flaw sensitivity length, the material exhibits flaw insensitivity. The flaw sensitivity length is a critical material property that reflects how the material is sensitive or insensitive to crack. However, the impact of crack length on the load-bearing process of material remains an open problem. In this work, we characterize the flaw sensitivity of a stretchable material, bacterial cellulose hydrogel, under monotonic and cyclic loadings. Through fracture and fatigue tests, we first determine that the hydrogel exhibits high fracture toughness and fatigue resistance. We next characterize the flaw sensitivity of the hydrogel through two visualized experimental methods. Photoelasticity observation on the stress distribution in samples during loading shows that the samples with cracks below 2 mm exhibit uniform stress distribution during the deformation process, while those with cracks above 2 mm experience stress concentration at crack tip. Scanning electron microscope observation on the microstructure morphology of samples under fixed stretch shows that the samples with cracks below 2 mm exhibit uniform alignment of nanofibers, while those with cracks above 2 mm exhibit more intense alignment and even bundling of nanofibers at crack tip. Similar trends are observed in the samples under cyclic loading, where the transition length is also about 2 mm. Notably, the flaw sensitivity lengths obtained by the visualized methods agree well with that obtained by direct measurement of rupture stress and theoretical estimations under monotonic and cyclic loadings. The methods offer novel way to study the flaw sensitivity of materials, thereby contributing to the exploration of failure mechanisms.

Accelerated Li Penetration and Crack Propagation Due to Mechanical Degradation of Sulfide-Based Solid Electrolyte.

This work presents quantitative investigations into the relationships between lithium dendrite growth in the defects of Li6PS5Cl (LPSCl) solid electrolyte (SE), crack nucleation and propagation in the SE, and the associated mechanical forces driving these dendrites and cracks. Two different growth modes for lithium dendrites are identified by ex situ scanning electron microscopy (SEM) observation: longitudinal cracking inside pores in the SE and lateral penetration along boundaries of the SE particles. These in situ TEM tests reveal that concentrated Li plating in a nano-sized defect on the LPSCl surface will lead to the nucleation and propagation of cracks into the LPSCl under a stress much smaller than the expected mechanical strength of the LPSCl material. This unexpected mechanical degradation is caused by a reduction in the mechanical strength of LPSCl during electrochemical charge/discharge cycling, resulting from a disorder in the crystal structure of LPSCl as revealed by DFT simulations. Due to this mechanical degradation of LPSCl, the threshold force necessary to initiate crack growth is much lower than the previously expected force to drive dendrite growth.

Lattice variation as a function of concentration and grain size in MgO–NiO solid solution system

The study aimed to understand how changes in crystal's size affect the lattice parameters and crystal structure of Mg1-xNixO solid solution for six X values ranging from x = 0 to x = 1. Mg1-xNixO was synthesized via two different wet-chemical techniques: the sol-gel and the microwave hydrothermal method, both followed by calcination at different temperatures of 673, 873, 1073, 1273 and 1473 K. As annealing caused grain growth, the varied temperature range allowed to examine a wide range of grain sizes. The lattice parameters and x values were determined from XRD (X-ray diffraction) peak positions and intensities respectively. The grain size was evaluated by XRD line profile analysis and supported by SEM (scanning electron microscope) observations. At the temperatures of 673 and 873 K grain size was in the nanometric range and from 1073 K and above grain size was in the micrometric range. A non-monotonic lattice variation versus grain size was found for each concentration. When grain size decreased there was a slight contraction, however for grain size in the nanometric range there was a severe lattice expansion. Both lattice parameter changes were explained by two effects acting together: contraction due to surface stress and expansion due to weakening of the ionic bonding at nanocrystalline particles. In this current research study, the lattice parameter was mapped in two dimensions: concentration and grain size. The findings of this study provided valuable insights into the lattice variation in the MgO–NiO solid solution system.

Development of a microfurnace dedicated to in situ scanning electron microscope observation up to 1300 °C. I. Concept, fabrication, and validation.

The development of a new heating system dedicated to in situ scanning electron microscope (SEM) experimentation at high temperatures is reported. This system, called FurnaSEM, is a compact microfurnace, enabling heat treatments up to 1300 °C. The choice of materials for the microfurnace is explained. The design of the microfurnace is optimized by iterations of numerical simulations, and the thermal characteristics of the microfurnace are calculated numerically. The numerical results obtained are compared with the thermal characteristics of a manufactured microfurnace, measured on a specially developed dedicated test bench. This test bench includes a working chamber simulating a SEM chamber equipped with a thermal camera. The results obtained during various qualification tests enabled us to determine the main technical characteristics of the FurnaSEM microfurnace: temperature profiles on the sample support surface, energy consumption at high temperatures, and the range of achievable thermal cycles.

Development of a microfurnace dedicated to in situ scanning electron microscope observation up to 1300 °C. II. Study of the thermal response of samples.

When conducting in situ experiments at high temperatures in a scanning electron microscope using microfurnaces, controlling the temperature of a sample of a few mm3 placed in the hot zone of the furnace can be a complex task. In most cases, the temperature of the sample is estimated by means of a thermocouple placed in the hot body of the furnace, and the assumption made is that the temperature of the furnace is the temperature of the sample. In this work, a detailed understanding of the thermal response of the sample placed in the hot zone of the furnace is proposed. Temperature differences due to contact resistance between the furnace surface and the sample, the nature of the sample, and the sample geometry are calculated with a numerical model and measured experimentally on a dedicated test bench. Three technical solutions (bonding, sandwiching, and mini-crucible) for limiting temperature differences between the furnace surface and sample are proposed and validated by numerical calculations and experimental measurements.

Development of a microfurnace dedicated to in situ scanning electron microscope observation up to 1300 °C. III. In situ high temperature experiments.

The FurnaSEM microfurnace was installed in the chamber of a scanning electron microscope to carry out in situ experiments at high temperatures and test its limits. The microfurnace was used in combination with different types of detectors (Everhart-Thornley for the collection of secondary electrons in a high vacuum, gas secondary electron detector for the specific collection of secondary electrons in the presence of gas, and Karmen© detector for the collection of backscattered electrons at high temperature). Experiments carried out on various samples (metal alloys and ceramics) show that the microfurnace operates in both high-vacuum and low-vacuum modes. Temperature ramp rates during temperature cycles applied to the sample range from 1 to 120 °C/min (temperature rise) and 1 to 480 °C/min (controlled and natural cooling). The maximum temperature at which images were recorded up to 25k × magnification was 1340 °C, with a residual air atmosphere of 120Pa. The choice of a flat furnace with the sample placed directly above it has enabled innovative experiments to be carried out, such as low-voltage imaging (using a shorter working distance-up to 10 mm-than is possible with conventional furnaces), 3D imaging (by tilting the stage by up to 10°), and high-temperature backscattered electron imaging (using a dedicated detector).

Rational design, synthesis, and antimicrobial evaluation of novel 1,2,4-trizaole-substituted 1,3,4-oxadiazole derivatives with a dual thioether moiety.

In this paper, a series of novel 1,2,4-trizaole-substituted 1,3,4-oxadiazole derivatives with a dual thioether moiety were constructed. The synthetic compounds were characterized by 1H NMR, 13C NMR, HRMS, and single crystal diffraction. The antimicrobial activities of title compounds against fungi (Pyricutaria oryzae Cav., Phomopsis sp., Botryosphaeria dothidea, cucumber Botrytis cinerea, tobacco Botrytis cinerea, blueberry Botrytis cinerea) and bacteria (Xanthomonas oryzae pv. oryzicola, Xoc; Xanthomonas axonopodis pv. citri, Xac) revealed these compounds possessed excellent antibacterial activity through mycelial growth rate method and turbidity method, respectively. Among them, compounds 7a, 7d, 7g, 7k, 7l, and 7n had the antibacterial inhibition rate of 90.68, 97.86, 93.61, 97.70, 97.26, and 92.34%, respectively. The EC50 values of 7a, 7d, 7g, 7k, 7l, and 7n were 58.31, 48.76, 58.50, 40.11, 38.15, and 46.99μg/mL, separately, superior to that of positive control pesticide thiodiazole copper (104.26μg/mL). The molecular docking simulation of compound 7l and glutathione s-transferase also confirmed its good activity. The in vivo bioassay toward Xac infected citrus leaves was also performed to evaluate the potential of compounds as efficient antibacterial reagent. Further study of antibacterial mechanism was also carried out, including extracellular polysaccharide production, permeability of bacterial membrane, and scanning electron microscope observations. The excellent antibacterial activities of these compounds provided a strong support for its application for preventing and control plant diseases.

Examining Mechanical Property Differences in Concrete with Natural and Synthetic Fiber Additives

The rapid growth of Natural Fiber Laminate (NFL) innovation is a direct response to environmental challenges, positioning these materials as superior alternatives to synthetic fiber composites. This paper delved into the outcomes of an extensive experimental study investigating the influence of sisal fiber (SLF), banana fiber (BF), and glass fiber (GF) on the mechanical and microstructural characteristics of concrete. The water absorption curves were established for sisal fiber concrete (SLFC), banana fiber concrete (BFC), and glass fiber concrete (GFC). Furthermore, Scanning Electron Microscope (SEM) observations were conducted to perform microanalysis and failure analysis of the tested specimens. The results revealed significant improvements in the concrete containing fibers compared to its counterpart in fiber-free concrete. For mixtures with a water-to-binder (W/B) ratio of 0.3, the most optimal mix (GF-30-135) showed improvements in compressive strength, flexural strength, and splitting tensile strengths by 4.13%, 8.93%, and 10.10%, respectively. On the other hand, for W/B of 0.4, mix GF-30-135 showed improvements of 5.05%, 8.55%, and 11.60%, respectively. Furthermore, as the fiber content increased, microscopic analyses revealed a weakening of the bond between the fibers and the rest of the matrix, contributing to the deterioration of the mechanical properties.

Effect of a phthalate derivative purified from Bacillus zhangzhouensis SK4 on quorum sensing regulated virulence factors of Pseudomonas aeruginosa

Pseudomonas aeruginosa causes life-threatening diseases and is resistant to almost all conventional antibiotics. The quorum sensing (QS) system of P. aeruginosa contributes to many pathogenic factors some of which are pigment production, motility, and biofilm. The disruption of quorum sensing system may be an impactful strategy to deal with infections. The present study investigates the anti-quorum sensing property of a bioactive molecule extracted from marine epibiotic bacteria present on the surface of seaweeds. Among all the isolates tested against monitor strain Chromobacterium violaceum (MTCC 2656), the one with the highest activity was identified as Bacillus zhangzhouensis SK4. The culture supernatant was extracted with chloroform which was then partially purified by TLC and column chromatography. The probable anti-QS compound was identified as 1,2-benzenedicarboxylic acid, bis (2-methylpropyl ester) by GC-MS and NMR analysis. The treatment of P. aeruginosa MCC 3457 with the lead compound resulted in the reduced production of pyocyanin, rhamnolipids, exopolysaccharide, biofilm, and motility. The observations of light and scanning electron microscopy also supported the biofilm inhibition. The lead compound showed synergism with the meropenem antibiotic and significantly reduced MIC. The molecular docking and pharmacokinetics study predicted 1, 2-benzenedicarboxylic acid, bis (2-methylpropyl ester), a phthalate derivative as a good drug candidate. The molecular dynamics study was also performed to check the stability of the lead compound and LasR complex. Further, lead compounds did not exhibit any cytotoxicity when tested on human embryonic kidney cells. As per our knowledge, this is the first report on the anti-QS activity of B. zhangzhouensis SK4, indicating that epibiotic bacteria can be a possible source of novel compounds to deal with the multidrug resistance phenomenon.

Dynamic Climate Influence on Magnesium Isotope Variation in Saline Lacustrine Dolomite: A Case Study of the Qianjiang Formation, Jianghan Basin

The investigation of magnesium (Mg) isotopes in dolomite has mainly focused on marine dolomite environments, leaving a significant gap in the understanding of their dynamics within lacustrine settings, especially in saline lake basins. In this study, a total of 16 sediment core samples from Well BX-7 in the Qianjiang Depression were sequentially selected for scanning electron microscope observation, whole-rock analysis for major and minor elements, and isotopic measurements including δ18Ocarb, δ13Ccarb, δ26Mgdol, and δ26MgSi. In addition, two intact cores were subjected to detailed analysis on the centimeter scale. Sedimentation models were established to elucidate dolomite formation under contrasting climatic conditions, specifically humid climates with a significant riverine Mg input versus relatively dry conditions with a lower Mg input. Furthermore, a quantitative model was developed to assess the magnesium flux and isotopic mass balance within lacustrine systems, simulating the magnesium isotope variations in lake water under different climatic scenarios. The dolomite sample data at a smaller scale (sampling interval ≈ 3~5 mm) demonstrate a consistent trend with the established model, providing additional confirmation of its reliability. Dolomite precipitated under humid climatic conditions exhibits a lower and relatively stable δ26Mgdol, lower δ18O, and higher CIA, indicating higher river inputs and relatively stable Mg isotope values of lake water controlled by river input. Nevertheless, dolomite formed under relatively dry climatic conditions shows a relatively high δ26Mgdol, higher δ18O, and lower CIA, suggesting reduced river inputs and weathering intensity, as well as relatively high magnesium isotope values of the lake water controlled by dolomite precipitation. This study contributes to the understanding of magnesium isotopes in lacustrine dolomite systems.

Compressive Fracture Behavior of Zirconia/Resin Composites Prepared by Fused Deposition Modeling Combined with Vacuum Infiltration.

Although bioceramic materials exhibit good biocompatibilities and bone conductivities, their high brittleness and low toughness properties limit their applications. Zirconia (ZrO2)/resin composites with idealized structures and properties were prepared by fused deposition modeling (FDM) combined with a vacuum infiltration process. The porous structure was prepared using the FDM three-dimensional printing technology, with granular zirconia as the raw material, and the relationship between the pore shape, pore size, and deformation was discussed. The results showed that square pores were more suitable than honeycomb pores for printing small pore sizes, and the resolution was high. Scanning electron microscopy observations showed that the superposition of multiple printing paths promoted the emergence of hole defects. The effects of the resin and the pore shape on the compressive strengths of the composites were studied. It was found that the compressive strengths of the honeycomb pore ZrO2/resin composites and porous ceramics were superior to those of the square pore samples. The introduction of the resin had a significant effect on the compressive strengths of the composites. The compressive strength increased in the direction perpendicular to the pores, while it decreased in the direction parallel to the pores.

Optimization of method for cross-section hydrogels preparation using high-pressure freezing.

High-pressure water freeze fracturing is a method for preparing water-containing samples such as hydrogels for scanning electron microscopy (SEM), in which a sample is placed in a divisible pressure vessel, filled with water, sealed, frozen with liquid nitrogen and then vacuum dried after the vessel is divided. The pressure (∼200 MPa) generated by the phase transition from water to ice is expected to inhibit ice crystal formation that causes large deformation of microstructure in the sample. To maximize the useable sample size, where SEM observation is not affected by ice crystal growth, preparation conditions including the size of pressure vessel were examined in this work. Using pressure vessels 8.0 mm, 5.5 mm and 4.5 mm in diameter, agarose gel, gelatin gel, wheat starch hydrogel, wheat flour noodle and cellulose hydrogel were used to prepare SEM samples. With agarose gel, an area of 3.6 mm in diameter in the 5.5 mm vessel was achieved as the maximum size of the area observable without ice crystal growth. The observable size of other samples was comparable, except for gelatin gel. As a result, observation of the three-dimensional network structure of hydrogels could be performed over a wider range than with the conventional method without shredding or chemical treatment of the samples. Additionally, usability of agarose gel for sample support matrix in high-pressure water freeze fracturing was demonstrated.

Research on the Grinding Process of Superhard Particles in the Fluidized Bed Opposed Jet Mill Based on the CFD-DEM Methodology

The process of superhard particle breakage in the grinding zone of the fluidized bed opposed jet mill is investigated using the CFD-DEM (computational fluid dynamics-discrete element method) coupling method with the Tavares UFRJ Breakage Model in the present study. The effects of structural and operational parameters, such as target plate structure, nozzle position, air inlet velocity, and feed rate, on the equipment stress distribution, airflow velocity, pressure field, particle velocity, and cumulative particle size distribution are thoroughly studied to determine the optimal structural and operational parameters. Experimental validation is conducted, including scanning electron microscope (SEM) observation of particle morphology and analysis of particle size distribution of ground product particles. The simulation results indicate that the wear rate of the structure without a target plate is lower than that of the structure with a target plate in the grinding central zone. Therefore, the structure without a target plate is chosen for further investigation. The cumulative particle size distribution after grinding is influenced by nozzle position, air inlet velocity, and feed rate. The particle D50 is positively correlated with nozzle spacing and feed rate, while it is negatively correlated with air inlet velocity. The optimal grinding effect is achieved when the distance between the nozzle and the center of the grinding zone ranges from 52.5 mm to 72.55 mm, the air inlet velocity is 950 m/s, and the feed rate is 10.5 g/s. Through experimental investigation, it has been observed that when the feed rate is 10 g/s, the particle size distribution becomes more uniform. Furthermore, consistent trends in the cumulative particle size distribution in the experiment and simulation results can be found, which validates the present numerical model. It was observed that particles at low feed rates retain certain angular edges, while particle roundness increases at high feed rates.

Hyaluronic Acid‐based Cell‐free Composite Scaffold Promotes Osteochondral Repair In Vitro by Upregulating Osteogenic‐ and Chondrogenic‐Specific Gene Expressions

Osteochondral defects pose a significant challenge in clinical practice, leading to increased medical care, diminished quality of life for patients, and elevated economic burden. The restoration of osteochondral defects, particularly in cartilage, is limited by its finite repair capacity and complex architecture. Treatment based on regenerative therapies acclaims the favorable alternative to contemporary procedures. Studies reveal that engineered biomaterials hold the significant importance in stimulating tissue repair with minimal cost and risks. In this study, a porous composite scaffold is developed, where host cells infiltrate and create the microenvironment for cellular adhesion and enhanced differentiation. Thus, a composite scaffold composed of natural glycosaminoglycan hyaluronic acid (HA), the protein component fibrin, bioceramic nanohydroxyapatite (nHAP), and graphene oxide (GO) is fabricated. Scanning electron microscopy observation and physiochemical characterization reveal an interconnected pore structure, optimum swelling potential, high porosity (80.14%), controlled biodegradation, high mechanical properties, and mineralization. Evaluation of scaffold's biocompatibility using osteoblast – like MG‐63 cells – shows adequate viability, cell adhesion, and osteoinductive potential. The upregulated expressions of osteogenic and chondrogenic genes OCN, ALP, COL1A1, ACAN, SOX9, and COL2A1 promote mineralization and extracellular matrix formation. These findings suggest that the composite scaffold HA‐GO‐F‐nHAP exhibits promising potential for osteochondral repair.

Lightweight Biobased Polyurethane Composites Derived from Liquefied Polyol Reinforced by Biomass Sources with High Mechanical Property and Enhanced Fire-Resistance Performance.

Lightweight biobased insulation polyurethane (BPU) composite foams with high fire-resistance efficiency are interested in building effective energy and low environmental impact today. This study focuses on manufacturing lightweight BPU from liquefied bamboo polyols and biomass resources, including rice husk and wood flour. Then, they are combined with three flame retardant (FR) additives, such as aluminum diethyl phosphinate, aluminum trihydroxide, and diammonium phosphate, to improve their fire resistance performance. The physicochemical properties, microstructure, thermal stability, mechanical properties, and flame-retardant properties of the BPU composites are characterized to optimize their compromise properties. The results showed that composites with optimized FRs achieved UL94 V-0 and those with nonoptimized FRs reached UL94 HB. The limiting oxygen index exhibited that the fire resistance of BPU composites could increase up to 21-37% within FR additives. In addition, the thermal stability of BPU composites was significantly improved in a temperature range of 300-700 °C and the compressive strength of the BPU composites was also enhanced with the presence of FRs. The scanning electron microscopy observation showed an influence of FRs on the morphology and cell size of the BPU composites. The bio-PU-derived samples in this study showed significantly low thermal conductivity values, demonstrating their remarkable thermal insulation effectiveness.