Search

Packaging insulation materials with high thermal conductivity and excellent dielectric properties are favorable to meet the high demand and rapid development of third generation power semiconductors. In this study, we propose to improve the thermal conductivity of epoxy resin (EP) by incorporating a three-dimensional boron nitride thermally conductive network. Detailedly, polyurethane foam (PU) was used as a supporter, and boron nitride nanosheets (BNNSs) were loaded onto the PU supporter through chemical bonding (BNNS@PU). After immersing BNNS@PU into the EP resin, EP-based thermally conductive composites were prepared by vacuum-assisted impregnation. Fourier transform infrared spectrometer and scanning electron microscope were used to characterize the chemical bonding and morphological structure of BNNS@PU, respectively. The content of BNNS in BNNS@PU/EP composites was quantitatively analyzed by TGA. The results show that the thermal conductivity of the BNNS@PU/EP composites reaches 0.521 W/m K with an enhancement rate η of 30.89 at an ultra-low BNNS filler content (5.93 wt. %). Additionally, the BNNS@PU/EP composites have excellent dielectric properties with the frequency range from 101 to 106 Hz. This paper provides an interesting idea for developing high thermal conductivity insulating materials used for power semiconductor packaging. [ABSTRACT FROM AUTHOR]

Over the last two decades, Electron Energy Loss Spectroscopy (EELS) imaging with a scanning transmission electron microscope has emerged as a technique of choice for visualizing complex chemical, electronic, plasmonic, and phononic phenomena in complex materials and structures. The availability of the EELS data necessitates the development of methods to analyze multidimensional data sets with complex spatial and energy structures. Traditionally, the analysis of these data sets has been based on analysis of individual spectra, one at a time, whereas the spatial structure and correlations between individual spatial pixels containing the relevant information of the physics of underpinning processes have generally been ignored and analyzed only via the visualization as 2D maps. Here, we develop a machine learning-based approach and workflows for the analysis of spatial structures in 3D EELS data sets using a combination of dimensionality reduction and multichannel rotationally invariant variational autoencoders. This approach is illustrated for the analysis of both the plasmonic phenomena in a system of nanowires and in the core excitations in functional oxides using low loss and core-loss EELS, respectively. The code developed in this manuscript is open sourced and freely available and provided as a Jupyter notebook for the interested reader. [ABSTRACT FROM AUTHOR]

Low-energy ion beam irradiation, combined with the introduction of impurities, presents a promising approach for nanopatterning silicon (Si) surfaces. In this research, we investigate the surface evolution of Si (100) surfaces irradiated by 75 eV helium (He) plasma, in the presence of tantalum (Ta), traditionally regarded as an impurity incapable of initiating pattern formation, as evidenced in prior studies. The Ta impurities are pre-deposited onto the Si surfaces using the magnetron sputtering method, which offers a more controlled and quantifiable approach compared with the conventional co-deposition route. After irradiation at 800 K, dense cone arrays are produced on the Si surface. The growth of the cones is explored for fluence spanning (1–10) × 1025 m−2. The cross-sectional scanning electron microscope images indicate that the cone lengths and base width are well characterized by t1/2 dependence. The kinetics of the cone growth follow Fick's law, characterized by an effective diffusive mechanism with the coefficients of diffusion: D = 6.49 ± 0.83 × 10−16 m−2 s−1. Transmission electron microscope observations reveal that the cone has distinct inner and outer parts with different microstructures and a clear interface. The growth mechanism of these cones is elucidated as a composite process involving preferential sputtering, the destabilizing influence of He bubbles, and the migration of adatoms. [ABSTRACT FROM AUTHOR]

The scanning electron microscope (SEM) recordings of dynamic nano-electromechanical systems (NEMS) are difficult to analyze due to the noise caused by low frame rate, insufficient resolution, and blurriness induced by applied electric potentials. Here, we develop an image processing platform enhanced by the physics of the underlying system to track the motion of buckling NEMS structures in the presence of high noise levels. The algorithm is composed of an image filter, two data filters, and a nonlinear regression model, which utilizes the expected form of the physical solution. The method was applied to the recordings of a NEMS beam about 150 nm wide, undergoing intra- and inter-well post-buckling states with a transition rate of approximately 0.5 Hz. The algorithm can track the dynamical motion of the NEMS and capture the dependency of deflection amplitude on the compressive force on the beam. With the help of the proposed algorithm, the transition from inter-well to intra-well motion is clearly resolved for buckling NEMS imaged under SEM. [ABSTRACT FROM AUTHOR]

A non-destructive method for detecting sub-micrometer-sized micropipes on an entire wafer surface is investigated. Since it is difficult to detect sub-micrometer-sized micropipes due to their small core size, a non-destructively and accurately detecting method is required. To solve the issue, we focus on a characteristic depression generated around micropipes, namely, line-shaped depressions. In this paper, the location of line-shaped depressions is identified by using optical inspection, and the line-shaped depressions are distinguished whether micropipes exhibit line-shaped depression or not by using mirror electron microscope observation as high-resolution inspection. The accuracy of the distinction results is confirmed by scanning electron microscope observation, and electrical characteristics of the P–N diode are fabricated using the inspected wafer. Furthermore, the sub-micrometer-sized micropipes are observed at the sites of leakage current identified by emission microscopy. Additionally, device simulation of the blocking-voltage characteristics of P–N diodes suggests that the increase in leakage current depends on the electric field at the sub-micrometer-sized micropipes, regardless of their core size. [ABSTRACT FROM AUTHOR]

Gastropods forage with their radula, a thin chitinous membrane with embedded teeth, which scratch across the substrate to lose food particles. During this interaction, the risk of loosening particles is obvious without having a specialized mechanism holding them on the tooth surface. As mucus secretions are essential in molluscan life cycles and the locomotion and attachment gels are known to have an instant high adhesion, we have hypothesized that the saliva could support particle retention during feeding. As adhesion of snail saliva was not studied before, we present here an experimental setup to test its particle-binding capacity using a large land snail (Lissachatina fulica, Stylommatophora, Heterobranchia). This experiment was also applied to the gels produced by the snail foot for comparison and can be potentially applied to various fluids present at a small volume in the future. We found, that the saliva has high particle retention capacity that is comparable to the foot glue of the snail. To gain some insight into the properties of the saliva, we additionally studied it in the scanning electron microscope, estimated its viscosity in a de-wetting experiment, and investigated its elemental composition using energy dispersive X-ray spectroscopy reveling higher contents of Ca, Zn and other potential cross-linkers similar to those found in the glue. [ABSTRACT FROM AUTHOR]

In recent years, precision and accuracy for a more precise critical dimension (CD) control have been required in CD measurement technology. CD distortion between the measurement by a critical dimension scanning electron microscope (CD-SEM) and a reference tool is the most important factor for a more accurate CD measurement. CD bias varies by a CD-SEM and a pattern condition. Therefore, it is urgently needed to identify, characterize, and quantify those parameters that may or may not affect the CD measurement by a CD-SEM. The sensitivity of the Monte Carlo simulated CD-SEM images with multiple physical modeling components has been studied previously. In this study, we demonstrate that the work function and elastic scattering potential models have a significant impact on secondary electron emission intensity, but their influence on the shape of the linescan profile is small, and other factors like the optical energy loss function and dielectric function models have even smaller effects. We have evaluated the uncertainty in the linescan profiles of Si line structures with different sidewall angles due to several different physical factors. It is found that when the CD is evaluated by a peak/valley method, the uncertainty of the CD is negligible. Therefore, it is concluded that the CD value and its related uncertainty are not critically related to the physical factors of the present Monte Carlo simulation model but rely dominantly on the line structure and electron beam parameters. [ABSTRACT FROM AUTHOR]

We report on the metrological characterization of the emission from a germanium-vacancy center in diamond under a microfabricated solid immersion lens in a confocal laser-scanning microscope setup. Ge ions were implanted into a synthetic diamond at 3 MeV, and germanium-vacancy centers were then formed by subsequent annealing. Afterward, solid immersion lenses were fabricated in a focused ion beam scanning electron microscope. The photoluminescence was investigated at room temperature in terms of the spectral distribution, the excited state lifetime, the second-order correlation function, and the saturation behavior, proving simultaneous high single-photon purity and high brightness. Two methods were exploited to minimize the residual multi-photon probability: spectral filtering and temporal filtering. According to these results, we assume that Raman scattered photons and emission from neighboring color centers play an important role in the residual multi-photon emission probability. The system efficiency of the single-photon source was investigated and found to be in accordance with the value calculated from all sources of loss in the setup. The branching ratio of the germanium-vacancy center for the decay into the ground state and into metastable state was calculated. The results enable the usage of the single-photon source in future quantum radiometric experiments. [ABSTRACT FROM AUTHOR]

Because of their full compatibility with CMOS technology, HfO2-based ferroelectrics, and especially Hf0.5Zr0.5O2 (HZO), attract a lot of attention. However, the overwhelming majority of measurement techniques provides only information about the cumulative electrical response of many domains of HZO, i.e., at the macroscopic level. So far, only piezoresponse force microscopy technique was applied to visualize distinct ferroelectric domains in HZO and to analyze the local switching behavior in the microscopic level. This work introduces the possibility of using electron beam-induced current (EBIC) technique in the scanning electron microscope to visualize the gradual polarization reversal of HZO and to obtain the local polarization dynamics. We show that although the local EBIC signal is affected by surrounding domains, studying the variations in the ferroelectric response of individual domains as well as the spread of the local stiffness and local imprint is possible by this method. Besides, we show the connection between the EBIC current and an electric field across passive non-ferroelectric layers at interfaces between HZO and metal electrodes, which opens up additional opportunities to use the EBIC technique for investigations of interface-dependent properties of HZO ferroelectrics in the future. [ABSTRACT FROM AUTHOR]

Because of their full compatibility with CMOS technology, HfO2-based ferroelectrics, and especially Hf0.5Zr0.5O2 (HZO), attract a lot of attention. However, the overwhelming majority of measurement techniques provides only information about the cumulative electrical response of many domains of HZO, i.e., at the macroscopic level. So far, only piezoresponse force microscopy technique was applied to visualize distinct ferroelectric domains in HZO and to analyze the local switching behavior in the microscopic level. This work introduces the possibility of using electron beam-induced current (EBIC) technique in the scanning electron microscope to visualize the gradual polarization reversal of HZO and to obtain the local polarization dynamics. We show that although the local EBIC signal is affected by surrounding domains, studying the variations in the ferroelectric response of individual domains as well as the spread of the local stiffness and local imprint is possible by this method. Besides, we show the connection between the EBIC current and an electric field across passive non-ferroelectric layers at interfaces between HZO and metal electrodes, which opens up additional opportunities to use the EBIC technique for investigations of interface-dependent properties of HZO ferroelectrics in the future. [ABSTRACT FROM AUTHOR]

BACKGROUND: Polyvinylidene fluoride (PVDF) with piezoelectric properties, good biocompatibility and nontoxicity make it a suitable candidate for periosteal repair. OBJECTIVE: To evaluate the cytotoxicity of PVDF bionic periosteum by electrospinning with zinc and magnesium ions in vitro. METHODS: Pure PVDF, zinc-doped PVDF, magnesium-doped PVDF and Zinc-magnesium ion PVDF piezoelectric bionic periosteum were prepared by electrospinning technology, respectively. They were named PVDF, PVDF-Zn, PVDF-Mg and PVDF-Zn-Mg, in which the mass fraction of zinc and magnesium ions were all 1%. Osteoblasts and vascular endothelial cells were co-cultured with four groups of bionic periosteum. Cell compatibility of bionic periosteum was determined by alkaline phosphatase staining, CD31 immunofluorescence staining, and scanning electron microscopy. RESULTS AND CONCLUSION: (1) Osteoblasts: Alkaline phosphatase staining after 7 days of culture showed that the PVDF-Zn group secreted more alkaline phosphatase than the other three groups. Under a scanning electron microscopy, after 1 day of culture, the cells had a certain spread on the surface of PVDF-Mg and PVDF-Zn-Mg bionic periosteum, and the pseudopod extended to all sides. On day 3, the cell edge of each group extended pseudopods to the material. By days 5 and 7, the cells were fully spread, well grown and firmly covered the surface of the fibers, and the cellular pseudopods extended around and into the interstitial space of the fibers. CCK-8 assay showed that the cell proliferation on the bionic periosteum of each group showed an increasing trend over time and the relative proliferation rate of cells at 1, 3, 5, and 7 days was ≥75%, and the cytotoxicity was ≤ grade 1. (2) Vascular endothelial cells: CD31 immunofluorescence staining for 3 days showed that the cells adhered and spread well on the bionic periosteum of each group and connected with each other, and the number of cells in the PVDF-Zn-Mg group was more than that in the other three groups. Under scanning electron microscope, the cells began to adhere to the surface of each group of fibers after 1 and 3 days of culture. On day 5, the cells were well spread on the surface of the fibers and extended obvious pseudopods. On day 7, the cells on the PVDF-Mg and PVDF-Zn-Mg bionic periosteum grew in multiple layers and extended the pseudopod into the fibrous void. CCK-8 assay showed that the cell proliferation on the bionic periosteum of each group showed a downward trend over time, and the relative proliferation rate of cells at 1, 3, 5 and 7 days was ≥125%, and the cytotoxicity was grade 0. (3) The results showed that Zn-Mg electrospun PVDF piezoelectric bionic periosteum had good cytocompatibility. [ABSTRACT FROM AUTHOR]

This research explores the adsorption (AD) of diclofenac sodium (DS) onto a Hydrothermally produced activated carbon impregnated with ZnO (HTC-AC/ZnO) surface, considering various factors such as initial concentration (IC), adsorbent dose, contact time, and pH. The characterization of HTC-AC/ZnO was performed using X-ray diffractometer (XRD), scanning electron microscope (SEM), Fourier-transform infrared spectroscopy (FTIR), and nitrogen physisorption spectroscopy (BET). Tests were conducted with different adsorbent doses (0.5–4 g/L) at 303 K and various initial diclofenac concentrations (ranging from 50 mg/L to 250 mg/L) to observe their effects. Additionally, pH values were altered from 2 to 12 to study their influence on AD. Kinetic studies, thermodynamic studies, and AD isotherm models were examined. The Temkin isotherm model (TIM) was found to be the most accurate for DS-AD on HTC-AC/ZnO. For DS-AD on HTC-AC/ZnO, pseudo-first-order models (PFOM), intraparticle diffusion model (IPDM), and pseudo-second-order models (PSOM) were applied, with a correlation coefficient of 0.945, indicating a good fit for PFOM. The kinetics suggested rapid adsorption. Notably, the HTC-AC/ZnO composite exhibited consistent AD characteristics across four consecutive cycles, with a removal efficiency exceeding 99.38%. This suggests that HTC-AC/ZnO is an appropriate and economically viable adsorbent for the elimination of DS from water-based solutions. The investigation provides compelling evidence that HTC-AC/ZnO is a viable adsorbent for the effective elimination of DS from water sources. [ABSTRACT FROM AUTHOR]

The low liquid limit silty soil in the North China plain area is generally unsuitable for direct use as roadbed and slope soil. In order to improve the performance of low liquid limit silty soil, xanthan gum was used as an improver. Through a series of tests, the improvement effect of xanthan gum on low liquid limit silty soil was studied. The test results showed that Xanthan gum as an improver could significantly improve the unconfined compressive strength of silty soil. With the increase in dosage and curing age, the unconfined compressive strength of improved silty soil continued to improve and eventually tended to stabilize. The optimal dosage and curing period were 2% and 7 days, respectively. In addition, Xanthan gum could greatly improve the permeability and disintegration of low liquid limit silty soil. The permeability coefficient of improved silty soil with a content of 0.75% Xanthan gum and a 7-day curing period was 4.73 × 10−4 m·s−1, which was only 1.10% of that of plain silty soil at the same curing period. After immersion in water for 12 h, the soil only experienced slight disintegration. The scanning electron microscope image showed that the gel generated by the hydration reaction of Xanthan gum could improve the compactness and integrity of the soil by filling the voids, thus significantly improving the mechanical and hydraulic properties of the low liquid limit silty soil. [ABSTRACT FROM AUTHOR]

A nanostructure of lithium-zinc copper ferrite (LiZnCu-Ferrite) prepared experimentally by the auto-combustion method depends on different parameters. The auto-combustion method operates at a temperature (160 °C) suitable for preparing the required nanostructure ferrite phase. The dependent composition was [Li 0.5-x Zn x Cu x Fe 2.5-x O 4 at (x = 0, 0.05, 0.15, 0.25, 0.35, and 0.45)]. A pre-firing at temperature (650 °C) was applied during the calcination process that was suitable to remove unwanted products. The sintering at temperature (800 °C) was suitable for a pelletized shape of ferrite samples. The X-ray diffraction (XRD) pattern showed a spinel structure of ferrite phase produced for all samples under study with the lattice constant in the range (8.345–8.368 Å) as a function of (x). The crystallite size was in the range (18.41–30.27 nm) calculated by the Scherrer method. The transmission electron microscope (TEM) showed a production of nanorods in the size range (10–45 nm) and nanoparticles in the size range (10–40 nm). There was a coincidence between the results of the XRD and TEM analyses. On the other hand, the scanning electron microscope (SEM) showed the surface morphology and the nature of grain size, which was a sign of the presence of nanostructure; it agreed with the XRD analysis. FTIR spectra showed evidence that the system Li0.5-xZnxCuxFe2.5-xO4 had spinal ferrite nanoparticles successfully prepared by sol-gel auto-combustion. A vibrating sample magnetometer (VSM) showed a change in magnetic parameters as compensation factor (x) increased for all composites of LiZnCu-ferrite such as saturation magnetization (Ms), initial magnetic permeability (μi), remanence (Mr), and coercive force (Hc) that measured from M − H loops. A saturation magnetization increased as a function of (x) and recorded a maximum value at (x = 0.15). While the coercivity, initial magnetic permeability (μi), and remanence magnetization enhanced as a function of (x) and recorded a maximum value at (x = 0.45). [ABSTRACT FROM AUTHOR]

The main objective of this study is to fabricate composite materials having excellent thermal, mechanical and electrical properties for thermal and electronic applications. In this work, strontium feldspar-containing composites (Sr-feldspar/cordierite and Sr-feldspar/Sr-osumilite) were prepared by solid-state sintering of SrO-containing cordierite (MgSrAl 4 Si 5 O 18)/borosilicate glass powder mixtures. The phase composition, physical properties and microstructure of sintered composites were investigated by X-ray diffraction technique, water displacement method and scanning electron microscope, respectively. Moreover, the thermal expansion coefficient, hardness, and electrical properties were also measured. The results of X-ray patterns revealed the crystallization of Sr-feldspar and cordierite in the composites that contain up to 20% borosilicate glass. On the other hand, the composites that include more than 20% glass, displayed the crystallization of Sr-feldspar and Sr-osumilite with little amount of cristobalite. The bulk density values of sintered composites were decreased from 2.41 to 1.84 g/cm3 with increasing the amount of added glass. The microhardness values were increased from 519 to 710 kg/mm2 with increasing the glass content. Low thermal expansion coefficient (2.65 × 10−6, 2.22 × 10−6, 3.45 × 10−6 and 4.26 × 10−6 K-1 for C0, CG91, CG73, CG55, respectively) and low dialectic constant (7–8.5) were obtained for the prepared composites. [ABSTRACT FROM AUTHOR]

The lack of concrete tensile stress endurance led to the invention of engineered cementitious composite. However, the absence of gravel from the mixture in addition to the high binder content may lead to high shrinkage strain. Therefore, a radical solution to this problem is worth to be anticipated. The importance of this research lies in investigating the long-term drying shrinkage strain of the engineered cementitious composite since there is a lack of information regarding this behavior. Mixes of 30 and 60 MPa strengths were produced with polyvinyl alcohol fibers PVA-ECC and polypropylene fibers PP-ECC. The drying shrinkage strain of PVA-ECC mixes has been compared to PP-ECC mixes for both short term (0–28 days) and long term (0–360 days). Results indicated that all PVA-ECC mixes exhibited lower drying shrinkage strains than PP-ECC mixes. The ultimate drying shrinkage strain was recorded to be 1200 microstrain at 28 days. The increment in drying shrinkage strain after 28 days was 5.6% in PVA-ECC mixes when compared to that in PP-ECC mixes which was 6.77%. For high strength levels, the drying shrinkage strain at the age of 360 days declared a reduction of 3.5% for PVA-ECC compared to PP-ECC mixes. Also, it was lower for mixes with 60 MPa (6.3%) than for mixes with 30 MPa (7.6%). Therefore, despite the higher cement content for mixes with 60 MPa strength, the higher fiber volume fraction and the higher PVA solution percentage restricted the drying shrinkage strain increment. The research also addresses some mechanical tests of engineered cementitious composite concrete such as compressive strength, flexural strength, and strain capacity that may provide a strong relation to the drying shrinkage behavior of the different mixes. The scanning electron microscope images were involved in this research to declare the impact of fiber types on the microstructure of the ECC mixes. [ABSTRACT FROM AUTHOR]

To investigate the reinforcing effect of nanoflower‐like hydroxyapatite (NFHA) in resin‐based dental composites, we synthesized a novel NFHA using microwave irradiation (MW), hydrothermal treatment (HT), and sonochemical synthesis (SS). Silanized NFHA was then used as the reinforcing filler in dental resin composites. We characterized the structure and morphology of various HA nanostructures using x‐ray diffraction, scanning electron microscope, and TEM. The mechanical performance of dental resin composites reinforced with silanized NFHA was measured using a universal testing machine. Spherical HA, synthesized through chemical precipitation (CP), served as the control group. One‐way analysis of variance was employed for the statistical analysis of the acquired data. The results demonstrate that the nanoflower morphology significantly was improved mechanical and physical properties. After conducting trials, the NFHA synthesized using MW and HT showed a substantial enhancement in mechanical and physical properties compared to the other structures. Therefore, it can be concluded that NFHA can serve as a novel reinforcing HA filler, providing regenerative properties to resin composites with sufficient mechanical strength. [ABSTRACT FROM AUTHOR]

Sodium‐ion batteries (SIBs) represent a viable substitute to lithium‐ion batteries due to their affordability and resource abundance. For SIBs, antimony (Sb) shows potential as anode material but is impeded by the high volumetric variations. Here the challenges of Sb sodium storage by introducing the nanostructured Cu substrate for enhanced Sb adhesion and morphology optimization is addressed, which is realized by fused deposition modeling (FDM) printing of Cu substrate, subsequent high‐temperature sintering, and electrodeposition of Sb. In SIBs, the Sb deposited on three dimensional (3D) printed Cu substrate performs improved cycling stability compared with that of Sb@Cu with commercial Cu foil substrate, which can be attributed to the nanostructure of the 3D‐Cu substrate. Such architecture of 3D‐Cu induces the generation of pine‐leaf‐like Sb clusters to promote stability and kinetics, and it aids the adhesion between the Sb cluster and 3D‐Cu substrate for preventing the Sb detachment and restructuring the Sb cluster to the robust porous ligament‐channel Sb framework. The morphology evolution, (de)sodiation mechanism, and gas evolution are explored by ex situ scanning electron microscope, operando X‐ray diffraction, and operando differential electrochemical mass spectrometry separately. The developed Sb@3D‐Cu anode offers a flexible pathway for constructing 3D‐printed self‐supported electrodes for SIBs. [ABSTRACT FROM AUTHOR]

This research paper focuses on the use of solid biomass waste, specifically a combination of Polyalthia longifolia seed (PLSF) and graphite (GH) powder, as reinforcements in vinyl ester (VE) composites. The composites were produced via the hand layup method, with the filler concentration varying from 0 to 15 wt% of PLSF and 0–9 wt% of graphite. The objective was to examine the influence of the hybrid filler on the mechanical characteristics of the composites. The mechanical properties of composites prepared from P. longifolia seeds and graphite powder were experimentally characterized. These properties included tensile strength, flexural strength, impact resistance, and hardness. The hybrid composite had a maximum tensile strength of 48.4 MPa, and its tensile modulus was 1.66 GPa. The hybrid filler at 15% wt% of PLSF and 6% of graphite has the highest flexural strength, which is around 148 MPa. The ultimate impact strength and hardness were measured to be 41.3 kJ/m2 and 44.5, respectively, after the addition of 15 and 6 wt% of hybrid filler. In comparison to neat vinyl ester resin, the PLSF/GH‐VE composites exhibited an increase in tensile, flexural, impact, and hardness of 2.69, 1.82, 3.03, and 1.59 times, respectively. Hybrid composite surfaces were analyzed using scanning electron microscopes to determine surface characteristics and fractured surfaces. In addition, the PLSF/GH‐VE composites have been utilized in the production of components for four‐wheelers. Highlights: Investigated the impact of hybrid filler‐reinforced vinyl ester composites.Mechanical and thermal properties were experimentally characterized.Surface characteristics and fractured surfaces were examined.PLSF/GH‐VE composites are used in producing components for four‐wheelers. [ABSTRACT FROM AUTHOR]

The biodegradable materials cannot meet the requirements as the agricultural film due to the poor UV resistance and antidripping performance. The work herein thus presented the development of the green‐based anti‐ultraviolet and antidripping multifunctional composite films using poly(butyleneadipate‐co‐terephthalate), microfibrillated cellulose (MFC), and soybean protein isolate (SPI) as the raw materials in the presence of other agents. The resulting composite films were systematically characterized using scanning electron microscope, thermogravimetry analysis (TG), UV, and rheometer measurements. The morphology changed obviously after introducing the MFC and SPI into the substrate film. In addition, the results indicated that the addition of MFC and SPI had a positive effect on the thermal stability and heat preservation of the film, respectively. The contact angle results indicated that SPI was an ideal antidripping agent and the MFC could be used as the release agent. The time of the first water drop of the film containing 2.5 g MFC and 2.0 g SPI was 6 min and 46 s, and the time of each 10 drops was less than 60 s, showing the advantages of using MFC as the release agent and SPI as the antidripping agent. The resulting multifunctional biodegradable films can be widely used in the agricultural and packaging fields. [ABSTRACT FROM AUTHOR]

This research delved into the structural, morphological, and magnetic characteristics of rare earth doped strontium ferrites (SrRE x Fe 12-x O 19 (x = 0.05–0.2, RE = La, Sm, Eu, Dy, Er, Lu)) synthesized via the sol-gel method. The dopant ion radius is correlated with the performance of the material to a certain extent. Barium and calcium doping and related iron deficiency state experiments were designed to substantiate the reciprocal dependence between ion radius and coercivity. X-ray diffraction results revealed that doping ions had the capacity to modify lattice dimensions. The lattice size does not exhibit a clear linear relationship with the radius of the doping ion, nor does it inherently correlate with the grain size. The scanning electron microscope demonstrated that ion doping had the capacity to influence the size of grains. A general consequence of rare earth doping is the reduction in the saturation magnetization of strontium ferrites. The lanthanide contraction effect significantly influences the changes in coercivity. It is noteworthy that the variations in lattice internal space induced by doping constitute a primary driving factor for the observed coercivity dependence on the radius of the doping ion. [ABSTRACT FROM AUTHOR]

Osteogenic differentiation and bone regeneration can be effectively aided by porous scaffolds with multiscale cellular structures, making it easier to repair defects in bone tissue. Due to the scarcity of pore-forming agents, it is extremely challenging to fabricate interconnected hierarchically porous zirconia at multi-scale. This work described a novel and straightforward method for directly imprinting a slurry containing two pore-forming agents (microspherical and filamentary) to produce strong and highly porous zirconia (ZrO 2) ceramics with four levels of porosity ranging from nanometers to millimeters. The concentration of hemp fibers significantly affected printability when the rheological behavior of a zirconia slurry was examined. Utilizing a scanning electron microscope (SEM) to monitor the development of powder interstices under various sintering techniques. The permeability performance was assessed when simulated plasma had fully filled the scaffolds. The structure had a high compressive strength of 24.18 MPa, a porosity of 80.9 %, an apparent porosity of 55.7 %, and took just 1.11 s to fill a scaffold that was 15 mm high. It is anticipated that the proposed route will be expanded to include various engineering materials for structural and practical applications. [ABSTRACT FROM AUTHOR]

Daqiuni clay is an aluminosilicate clay with unique properties that make it a promising ceramic precursor. Understanding its sintering behavior is crucial for quality control in manufacturing. This study aimed to investigate the phase evolution, densification process, and reaction kinetics during sintering of Daqiuni clay. A combination of X-ray diffraction (XRD), simultaneous thermogravimetric-differential scanning calorimetry (TG-DSC), scanning electron microscope (SEM) and Fourier transform infrared spectroscopy (FTIR) techniques were employed to comprehensively analyse the phase transformations. The densification behavior, apparent activation energies, and reaction mechanisms were elucidated through thermodilatometric analysis conducted at varying heating rates. Four stages were identified during sintering including dehydration, dehydroxylation, mullite formation, and partial melting. The maximum shrinkages at each stage were measured. Kissinger analysis yielded apparent activation energies of 122.90, 258.40, 361.98 and 348.69 kJ/mol for the dehydroxylation, mullite nucleation, mullite growth, and partial melting stages, respectively. The dehydroxylation and partial melting processes followed the mechanisms of 3rd order reaction and 3D diffusion. Mullite formation was a two-step nucleation and growth process following the JMA model. This study clarified the phase evolution of Daqiuni clay during sintering. [ABSTRACT FROM AUTHOR]

The chemical, physico‐mechanical, morphological, and thermal characteristics of alkali treated natural cellulosic sustainable eco‐friendly fiber from peduncle of Areca Catechu tree were investigated. Areca Catechu fruit peduncle fiber (ACFPF) treated with 5% (w/v) NaOH solution for 60 min is found as optimally alkali treated ACFPF (OAACFPF) witnessed an increase in cellulose content by 17%. Single fiber tensile test perceived that OAACFPF enhanced tensile strength by 12.9% and x‐ray diffraction analysis depicts crystallinity index of OAACFPF improved by 14.2% compared with ACFPF. Also, Fourier transform infrared spectroscopy analysis endorsed partial removal of amorphous contents from fibers due to alkali treatment. In addition, alkali treatment has enhanced thermal stability of OAACFPF from 226°C to 235°C verified through Thermogravimetric analysis. Likewise, Differential scanning calorimetry analysis confirmed improvement in thermal degradation temperature of OAACFPF after alkali treatment. Moreover, the rougher surface of OAACFPF confirmed through scanning electron microscope and atomic force microscopy is due to partial removal of amorphous contents thus ensuing in good interfacial bonding characteristics with the matrix during reinforcement for bio‐composite fabrication. The above findings validated OAACFPF as a worthy substitute to harmful synthetic fibers for development of eco‐friendly and sustainable bio‐composites. [ABSTRACT FROM AUTHOR]

This study focuses on improving the quality of MAPbI3‐based perovskite films by adjusting the concentration ratios of the methylammonium iodide (MAI) precursor using a two‐step sequential deposition method. The primary objective is to explore how altering the MAI concentration influences the microstrain, dislocation density, perovskite film quality, and their subsequent impact on the performance of perovskite solar cells. The examined device configuration CdS/MAPbI3/Spiro‐OMeTAD demonstrates impressive power conversion efficiency of 12.05%, Voc of 1.02 V, Jsc of 16.2 mA cm−2, and fill factor of 0.73. X‐ray diffraction and scanning electron microscope analyses show improved crystal quality and surface characteristics with reduced microstrain, dislocation density, larger crystal grains, and minimized pinholes. The investigation of MAPbI3's optical and electrical characteristics provides in‐depth insights, facilitating the optimization of MAI precursor concentrations for improved perovskite film development and enhanced solar cell performance. [ABSTRACT FROM AUTHOR]

The current work aims to explore the structural and optical properties of Cu1−xNixO/ZnO nanostructured heterojunctions for optoelectronic applications. ZnO nanostructures and different Cu1−xNixO/ZnO (x; 0, 0.05, 0.10, 0.15 and 0.20) nanostructured heterojunctions were prepared by spray pyrolysis procedure on glass substrates. The surfaces morphology of the samples was examined by a scanning electron microscope (SEM). The energy dispersive X-ray (EDX) microscope was utilized to examine the elemental analysis. The XRD measurements show that ZnO nanostructures possess a hexagonal wurtzite structure, while Cu1−xNixO nanostructures possess monoclinic structures. The FT-IR spectroscopy was performed to explore the chemical bondings and functional groups. The UV–visible-NIR spectrophotometer was used to investigate the optical properties. The optical constants (refractive index, extinction coefficient, dielectric constants, optical conductivity) of the prepared samples have been investigated. The first-order linear optical susceptibility, third-order optical susceptibility and nonlinear refractive index are also studied. The obtained results show that the optical parameters of Cu1−xNixO/ZnO heterojunction could be tuned through controlling the Ni content. These novel findings nominate Cu1−xNixO/ZnO nanostructured heterojunctions for a plenty of optical, photocatalytic and optoelectronic applications. [ABSTRACT FROM AUTHOR]

The composition and structure of Sherobod quartz sand and man-made waste were fully investigated using chemical, scanning electron microscope, X-ray, infrared spectroscopic and differential thermal analysis methods. It was found that the content of lead and manganese oxides in Handiza lead concentrate and manganese waste is 25 - 26 %, respectively, and silicon oxide in Sherabad quartz sand is more than 80 %. According to the results of chemical and physico-chemical analyzes of Sherabad quartz sand and man-made waste, it was found that they can be added as glass components by cleaning them from various additives. [ABSTRACT FROM AUTHOR]

The synthesis, physicochemical characterizations, and biological investigations on the chelation of the antibiotic medication enoxacin (EXN) with certain vital metal ions, such as platinum(IV), ruthenium(III), and iridium(III) are discussed in this study. These compounds structures were interpreted based on elemental analysis and spectral measurements (FTIR, 1H-NMR, UV-Vis electronic, and XRD). The findings show that there is same coordination pathway for the chelation behavior of enoxacin complexes: a monodentate manner. The Pt(IV), Ru(III), and Ir(III) complexes are coordinated through the N atom of the piperazine ring, which is an unusual mode of coordination for this class of compounds. The dissolved complexes in DMSO were found to have non-electrolyte nature based on their molar conductance measurements. The formula for these complexes is [Pt(EXN)3(H2O)2Cl] (1), [Ru(EXN)3(H2O)3] (2), and [Ir(EXN)3(H2O)3] (3). Using scanning electron microscope (SEM) analysis and Xray powder diffraction (XRD), the nano-scale range of the Pt(IV), Ru(III), and Ir(III) complexes has been determined. Results of in vitro cytotoxicity were examined using MCF-7 cells (human breast cancer cell line) and HepG-2 cells (human hepatocellular carcinoma) that had been grown. The cytotoxic activity of the metal complexes demonstrated a cytotoxic effect against the growth of human breast and liver cancer cell lines. [ABSTRACT FROM AUTHOR]

3D printing has witnessed a remarkable surge in popularity due to its flexibility in design and adaptability as a manufacturing technique to nearly each industrial area. This study focuses on harnessing the technological versatility of 3D printing by utilizing both standard poly lactic acid (PLA) and copper powder‐doped PLA to fabricate intricate structures through a layer‐by‐layer additive manufacturing process. The other innovation introduced here lies in the postprocessing step, which involves salt remelting. The mechanical properties of 3D‐printed standard test specimens undergo comprehensive assessment, encompassing bending and tensile evaluations, hardness measurements, density assessments, dimensional stability analyses, and wear resistance examinations. Utilizing copper powder‐doped PLA for the initial and final layers in XYZ‐oriented prints enables multimaterial printing, resulting in an ≈14% increase in tensile strength. Subsequently, subjecting this multimaterial composite to salt remelting elevates the strength enhancement to ≈16%, accompanied by a significant boost in rigidity by reducing voids in cross‐sectional area. In addition, scanning electron microscope images are captured, allowing for a detailed morphological analysis, which is then correlated with the findings of the various tests performed. This research unveils the potential of 3D printing technology in crafting materials with tailored mechanical properties, advancing its applicability in numerous industrial sectors. [ABSTRACT FROM AUTHOR]

To evaluate the effects of an ammonia-based and a water-based silver-containing solutions on bonding performance and matrix-metalloproteinases (MMPs) activity of a universal adhesive to dentin after 1 year of artificial aging. Mid-coronal dentin surfaces of 60 sound human molars were exposed and the following groups were formed according to the surface pre-treatment and etching mode of the universal adhesive (Zipbond Universal, SDI) (n = 10): G1) Zipbond in the self-etch mode (ZSE); G2) Riva Star (SDI) applied before ZSE; G3) Riva Star Aqua (SDI) applied before ZSE; G4) Zipbond in the etch-and-rinse mode (ZER); G5) Riva Star applied before ZER; G6) Riva Star Aqua applied before ZER. The specimens were sectioned and subjected to microtensile bond strength (µTBS) test at baseline (T 0) and after 12 months (T 12) of artificial storage. Scanning electron microscope (SEM) and energy dispersive spectroscopy analysis (EDS) were also conducted. Three additional molars per group were processed for the in situ zymography analysis at T 0 and T 12. Data were statistically analyzed (p < 0.05). Dentin pre-treatments and aging decreased bonding values, regardless of the etching mode (p < 0.05). No differences in µTBS were observed between the two silver-containing solutions, both at T 0 and T 12. Riva Star Aqua and etching significantly increased the MMPs activity, independent of the storage period (p < 0.05). Dentin surface pre-treatment with silver-containing solutions negatively affects the bonding performances of resin composite restorations placed with a universal adhesive. However, the ammonia-based product Riva Star might show better stability in the long term, due to lower activation of MMPs. • Silver-containing solutions lower bond strength of resin composite to sound dentin; • Riva Star might show better hybrid layer stability in the long term; • Riva Star Aqua has never been investigated before. [ABSTRACT FROM AUTHOR]

The present study focused on the histogenesis of the crop in quail embryos. The developmental sequence was recorded from day 10 of incubation to the hatching day (17th day) by gross anatomy, morphometric analysis and by using light and scanning electron microscope (SEM). Grossly, the crop was distinguished as an enlarged pouch of the cervical oesophagus on the 12th day of incubation. Histologically, the development of the crop began on the 10th day of incubation. The muscularis mucosae was observed as a small, thin layer of myoblast cells on the 10th day, then it appeared as longitudinally arranged smooth muscle fibres with progression of the developmental age till hatching day. The submucosal layer was also observed on the 10th day, while the lamina propria, muscular layer (inner circular and outer longitudinal layers of smooth muscle fibre) and glandular primordia were detected on the 12th day. The epithelial cells of crop revealed affinity for PAS stain and AB‐PAS on the 10th day of incubation till the 17th day, while the affinity for AB stain appeared on the 14th day of incubation. Additionally, the glandular cells showed the positive for AB, PAS and AB‐PAS on the 12th day of incubation. SEM sections showed variable sizes of the openings of the oesophageal glands. In conclusion, the present study provided a detailed overview of the histogenesis of the crop in quail embryos. [ABSTRACT FROM AUTHOR]

X-ray nanotomography is a powerful tool for the characterization of nanoscale materials and structures, but it is difficult to implement due to the competing requirements of X-ray flux and spot size. Due to this constraint, state-of-the-art nanotomography is predominantly performed at large synchrotron facilities. We present a laboratory-scale nanotomography instrument that achieves nanoscale spatial resolution while addressing the limitations of conventional tomography tools. The instrument combines the electron beam of a scanning electron microscope (SEM) with the precise, broadband X-ray detection of a superconducting transition-edge sensor (TES) microcalorimeter. The electron beam generates a highly focused X-ray spot on a metal target held micrometers away from the sample of interest, while the TES spectrometer isolates target photons with a high signal-to-noise ratio. This combination of a focused X-ray spot, energy-resolved X-ray detection, and unique system geometry enables nanoscale, element-specific X-ray imaging in a compact footprint. The proof of concept for this approach to X-ray nanotomography is demonstrated by imaging 160 nm features in three dimensions in six layers of a Cu-SiO2 integrated circuit, and a path toward finer resolution and enhanced imaging capabilities is discussed. [ABSTRACT FROM AUTHOR]

As a powerful imidazole antifungal drug, ketoconazole's low solubility (0.017 mg/mL), together with its odor and irritation, limited its clinical applications. The inclusion complex of ketoconazole with randomly methylated β-cyclodextrin was prepared by using an aqueous solution method after cyclodextrin selection through phase solubility studies, complexation methods, and condition selection through single factor and orthogonal strategies. The complex was confirmed by FTIR (Fourier-transform infrared spectroscopy), DSC (differential scanning calorimetry), TGA (thermogravimetric analysis), SEM (scanning electron microscope images), and NMR (Nuclear magnetic resonance) studies. Through complexation, the water solubility of ketoconazole in the complex was increased 17,000 times compared with that of ketoconazole alone, which is the best result so far for the ketoconazole water solubility study. In in vitro pharmacokinetic studies, ketoconazole in the complex can be 100% released in 75 min, and in in vivo pharmacokinetic studies in dogs, through the complexation, the Cmax was increased from 7.56 μg/mL to 13.58 µg/mL, and the AUC0~72 was increased from 22.69 μgh/mL to 50.19 μgh/mL, indicating that this ketoconazole complex can be used as a more efficient potential new anti-fungal drug. [ABSTRACT FROM AUTHOR]

P91 and P92 steels are widely used in nuclear and thermal power plant's high-temperature (650–700 °C) operating components. The welding procedure, base plate composition, filler material composition, and post-weld heat treatment (PWHT) significantly affect the metallurgical characterization of weldments at room temperature. This work focuses on joining P91 and P92 steel by the TIG welding with filler ER90S-B9. The study analyzes the materialization of coarse-grained HAZ (CGHAZ), inter-critical HAZ (ICHAZ), and fine grained HAZ (FGHAZ) under welded and PWHT. PWHT was conducted at 840 °C for 2, 4 and 6h. An optical microscopic (OM) scanning electron microscope (SEM) was employed to characterize the welded and PWHT samples. It was perceived that the tensile strength of PWHT increased as the heat treatment times increased from 2 to 6 h, while the hardness value decreased accordingly. The maximum tensile strength (594.71 MPa) was observed in PWHT_6 h, while the minimum tensile strength (537.52 MPa) was perceived in the as-welded sample. The PWHT_6h reveals the minimum hardness values (271.12 HV) at the fusion zone among all the conditions. The WFZ consisted of an untampered lath martensitic grain structure, demonstrating an average hardness value of 314.15 HV in the PWHT_2h condition. The hardness value in CGHAZ samples for as-welded, PWHT_2h, PWHT_4h, and PWHT_6h was observed at 456.85, 436.81, 368.63, and 327.41 HV, respectively. [ABSTRACT FROM AUTHOR]

Recycling crushed clay bricks (CCB) in concrete is a sustainable and cost-effective process. Huge quantities of crushed clay bricks waste cause many serious environmental problems around the world. To deal with this problem, crushed bricks were recycled in the concrete industry as an alternative to natural resources, and the brick powder was reused as a partial replacement for cement. The objective of this paper is to study the effect of crushed clay bricks on the characteristics of concrete. 7 concrete mixtures containing coarse crushed brick aggregate (CCBA) and fine crushed brick aggregate (FCBA) were prepared as a complete substitute for sand and dolomite, respectively. Clay brick powder (CBP) and silica fume were used as a partial substitute for cement by 5%, 10%, and 15% of its weight. The water-to-cement ratio was 0.35. For comparison, a control mixture was prepared. Various tests were conducted to evaluate the performance of concrete. The results showed that the workability of the different mixtures containing CCB decreased compared to that of the reference mixture. The compressive strength values of mixtures containing CCBA had a clear decrease compared to the reference mix at 7, 28, and 56 days of curing. The modulus of rupture results had the same path as compressive strength results. The thermal conductivity coefficient for mixtures including CCBA decreased compared to the control mix. Scanning Electron Microscope images indicated crystals of calcium silicate hydrate because of the pozzolanic interaction between the brick powder and the fine crushed clay bricks with calcium hydroxide. [ABSTRACT FROM AUTHOR]

The liquid-phase epitaxial growth (LPE) of GaN crystals on the MOCVD-GaN substrate using the Na-flux method was investigated under various growth times, 30, 60, 100, and 150 h. The morphology properties of as-grown GaN crystals were characterized by the scanning electron microscope (SEM). The variation of nitrogen concentration and supersaturation of GaN in the Ga-Na melt as a function of time is given computationally during the growth time of 150 h, as well as the distribution of nitrogen concentration for 30, 60, 100, and 150 h. In the early term of LPE growth (Stage I), the growth proceeds in a near-equilibrium laminar pattern at lower growth driving forces, corresponding to a screw dislocation growth mechanism. As the growth time extends, the GaN supersaturation in the Ga-Na melt increases with mass transfer continuing, leading to the mechanism of LPE growth changing from screw dislocation growth to continuous hexagonal pyramidal growth with deeper and deeper pit depths, and also thereby leading to the emergence of Stage II. A high level of GaN supersaturation in the solution could promote the growth along the vertical direction of Stage II but is detrimental to the layer growth of Stage I. Broadening the growth of Stage I could realize near-equilibrium growth of GaN crystals and improve the crystalline quality of epitaxial GaN crystals. The specific mechanisms of the different stages of GaN crystal growth were not clarified in the previous work. Through a combination of experimental and simulation calculations, the GaN crystal growth mechanism was discussed. Based on the growth mechanism acquired, the growth process may be effectively regulated to obtain high-quality GaN single crystals. [ABSTRACT FROM AUTHOR]

Gelatin is a collagen-derived biopolymer with high biocompatibility, commonly used in the production of wound dressing materials. Gelatin-based wound dressings, obtained through different processing methods, come with their own advantages and disadvantages depending on their physical structure. In this study, the effects of gelatin wound dressing materials with two different morphologies on wound healing are investigated in detail. The study investigated that the preparation of gelatin-based wound dressing materials using two different methods, followed by their chemical characterization and examination of their effects on biocompatibility and wound healing. To comprehend the impact of nanofiber structure and porous sponge structure on the wound healing process, the chemical structure of the prepared wound dressings was analyzed using Fourier Transform Infrared Spectrophotometer (FTIR). The morphological structure was visualized through Scanning Electron Microscope (SEM), the thermal properties were determined using Thermogravimetric Analyzer (TGA) and Differential Scanning Calorimeter (DSC). Additionally, the in vivo wound healing effects of gelatin-based wound dressings with different structures were evaluated through macroscopic observation and histological analysis in a dorsal region wound-healing rat model, monitored for 21 days. It was observed that wound healing materials with desired nanofiber and porous sponge structures were successfully obtained based on the SEM analysis. The gelatin nanofiber dressing showed a randomly oriented, bead-free, and smooth morphology with an average fiber diameter of approximately 1250 ± 0.35 nm, while the crosslinked gelatin sponge dressing had pore sizes ranging from 20 to 160 μm, and interconnected pore structures. The chemical structure remained unaltered according to FTIR graphs and these results were further supported by DSC and TGA graphs. Results from in vitro biocompatibility studies indicated that the wound dressing materials were biologically compatible, non-toxic, and did not cause irritation or sensitivity to the skin. Regarding in vivo analysis, it was determined that gelatin dressing materials were functional in the wound healing process, without the use of any auxiliary materials. [ABSTRACT FROM AUTHOR]

The integration of reformers into high-temperature polymer electrolyte membrane (HT-PEM) fuel cells presents a significant opportunity to improve fuel flexibility and cost-effectiveness. To understand their degradation, we applied two start–stop cycling procedures: one with pure H 2 and another with an 80 vol % H 2 and 20 vol % N 2 mix to simulate reformate gas. We also performed a load cycling test with H 2 as anode gas. The results indicated that degradation rate of pure H 2 start–stop cycling showed 306 μ V h−1, while load cycling demonstrated a degradation rate of 19.7 μ V h−1 for the current density of 0.2 A cm−2, and 88.2 μ V h−1 for the current density of 0.4 A cm−2. Start–stop cycling with diluted gas resulted in a constant voltage drop with a degradation rate of 3.129 mV h−1. Electrochemical impedance spectroscopy (EIS) indicated an increased ohmic resistance during start–stop cycling and higher charge transfer (high-frequency) and mass transport (low-frequency) resistance with nitrogen introduction. Scanning electron microscope results confirmed MEA degradation. In conclusion, start–stop cycling and anode gas dilution are stressors that accelerate HT-PEM fuel cell degradation, reducing its lifetime. • Start–stop and anode gas dilution degrade HT-PEM cells. • Degradation jumps from 306 μ V/h to 3.129 mV/h with dilution. • Low degradation (88.2 μ V/h) at 0.4 A/cm² under load cycling. • Anode dilution with nitrogen amplifies resistive effects. • SEM analysis confirmed physical degradation of MEA. [ABSTRACT FROM AUTHOR]

Purpose: The purpose of this paper is to study the high temperature oxidation behavior of Ti and C-added FeCoCrNiMn high entropy alloys (HEAs). Design/methodology/approach: Cyclic oxidation method was used to obtain the oxidation kinetic profile and oxidation rate. The microstructures of the surface and cross section of the samples after oxidation were characterized by X-ray diffraction (XRD) and scanning electron microscope (SEM). Findings: The results show that the microstructure of the alloy mainly consisted of FCC (Face-centered Cubic Structure) main phase and carbides (M7C3, M23C6 and TiC). With the increase of Ti and C content, the microhardness, strength and oxidation resistance of the alloy were effectively improved. After oxidation at a constant temperature of 800 °C for 100 h, the preferential oxidation of chromium in the chromium carbide determined the early formation of dense chromium oxide layers compared to the HEAs substrate, resulting in the optimal oxidation resistance of the TC30 alloy. Originality/value: More precipitated CrC can preferentially oxidize and rapidly form a dense Cr2O3 layer early in the oxidation, which will slow down the further oxidation of the alloy. [ABSTRACT FROM AUTHOR]

Purpose: In this paper, the authors aim to study the effect of hydrogen on the pitting corrosion behavior of Incoloy 825, a commonly used material for heat exchanger tubes in hydrogenated heat exchangers. Design/methodology/approach: The pitting initiation and propagation behaviors were investigated by electrochemical and chemical immersion experiments and observed and analyzed by scanning electron microscope and energy dispersive spectrometer methods. Findings: The results show that hydrogen significantly affects the electrochemical behavior of Incoloy 825; the self-corrosion potential decreased from −197 mV before hydrogen charging to −263 mV, −270 mV and −657 mV after hydrogen charging, and the corrosion current density increased from 0.049 µA/cm2 before hydrogen charging to 2.490 µA/cm2, 2.560 µA/cm2 and 2.780 µA/cm2 after hydrogen charging. The pitting susceptibility of the material increases. Originality/value: Hydrogen is enriched on the precipitate, and the pitting corrosion also initiates at that location. The synergistic effect of hydrogen and precipitate destroys the passive film on the metal surface and promotes pitting initiation. [ABSTRACT FROM AUTHOR]

Purpose: This paper aims to study the influence of microparticles on the surface cavitation behavior of 2Cr3WMoV steel; microparticle suspensions of different concentration, particle size, material and shape were prepared based on ultrasonic vibration cavitation experimental device. Design/methodology/approach: 2Cr3WMoV steel was taken as the research object for ultrasonic cavitation experiment. The morphology, quantity and distribution of cavitation pits were observed and analyzed by metallographic microscope and scanning electron microscope. Findings: The study findings showed that the surface cavitation process produced pinhole cavitation pits on the surface of 2Cr3WMoV steel. High temperature in the process led to oxidation and carbon precipitation on the material surface, resulting in the "rainbow ring" cavitation morphology. Both the concentration and size of microparticles affected the number of pits on the material surface. When the concentration of microparticles was 1 g/L, the number of pits reached the maximum, and when the size of microparticles was 20 µm, the number of pits reached the minimum. The microparticles of Fe3O4, Al2O3, SiC and SiO2 all increased the number of pits on the surface of 2Cr3WMoV steel. In addition, the distribution of pits of spherical microparticles was more concentrated than that of irregularly shaped microparticles in turbidity. Originality/value: Most of the current studies have not systematically focused on the effect of each factor of microparticles on the cavitation behavior when they act separately, and the results of the studies are more scattered and varied. At the same time, it has not been found to carry out the study of microparticle cavitation with 2Cr3WMoV steel as the research material, and there is a lack of relevant cavitation morphology and experimental data. [ABSTRACT FROM AUTHOR]

Background: Collagen, a critical structural protein found abundantly in animal skin and bones, has become increasingly recognized for its potential therapeutic role in skincare. Despite growing interest, the scientific evidence for the efficacy of collagen sheet masks remains limited. The principal objective of our study was to provide insights into the multifaceted role of collagen in skin health, with a specific focus on its application in collagen sheet masks. Methods: The effects of a collagen sheet mask consisting of >92% native bovine collagen were investigated. The soluble protein components of the collagen matrix were analyzed and the influence of soluble collagen components on fibroblast regulation was examined. Scanning Electron Microscope (SEM) analysis was performed for structural analysis and effect on irritated skin. Five different clinical studies were conducted, including a comparison of the diversity of the skin microbiome, the tolerance and local irritating reactions in atopic dermatitis, an evaluation of skin redness after UV radiation, wrinkle reduction, and hydration and skin roughness of the collagen mask in comparison to a pre‐soaked cellulose sheet mask. Results: The collagen mask contains soluble protein components, including small collagen peptides. The mask showed potential for promoting fibroblast activity. SEM analysis showed a native collagen structure similar to human dermis. The mask maintained the skin microbiome diversity and decreased skin pH levels. It demonstrated good tolerability on both intact and lesional skin and had a significant effect in reducing erythema caused by UV radiation compared to other skincare products. It showed significant improvements in skin hydration and the volume of eye wrinkles and was more effective than pre‐soaked cellulose sheet masks. Conclusion: Collagen sheet masks have the potential to positively impact skin health and appearance by increasing hydration, reducing erythema, minimizing wrinkles, and maintaining a healthy skin microbiome and skin barrier. [ABSTRACT FROM AUTHOR]

Multi-walled carbon nanotubes (MWCNTs) have significant environmental concerns for soil, water and ecosystems. Since their harmful effects on human health, including respiratory disease, they are considered dangerous substances. Thus, it is required to discover a constructive solution to decrease of MWCNT toxicity. Due to their high degradability, white rot and soft rot fungi have been used in the biodegradation of various pollutants. In this study, we evaluated the ability of native Iranian white and soft rot fungi to degrade MWCNTs mainly by means of dynamic light scattering (DLS) and surface charge measurement. In this regard, growth kinetics, CO2 and protein production, size, surface charge and pH change were measured. Continuous Raman spectroscopy, scanning electron microscope (SEM) and transmission electron microscope (TEM) imaging were carried out to detect the process of degradation. The results showed that the morphology, arrangement, size and diameter of MWCNTs were modified due to fungal degradation. The cytotoxicity of treated MWCNTs was determined by the MTT test. The results indicated that native Iranian white and soft rot fungi have a significant ability for degradation of MWCNTs. Furthermore, it could be concluded that fungal treatment could reduce the toxicity of MWCNTs and the best result was achieved in 500 ppm MWCNTs for Trichoderma sp. The activities of oxidative enzymes such as laccase, manganese peroxidase (MnP) and lignin peroxidase (LiP) were measured to determine the mechanism of degradation. Enzyme assays have suggested that these oxidising enzymes especially laccase might play a key role in the degradation of MWCNTs in white rot and soft rot fungi. The overall results confirmed the reproductive ability of Trichoderma sp. WF29 as a soft rot and two white rot fungi Irpex lacteus WF36 and Trametes versicolor to degrade MWCNT. [ABSTRACT FROM AUTHOR]

This research focuses on synthesizing polyvinyl alcohol (PVA) nanocomposite film adopted with 3–9 wt% of nano-sized (50 nm) titanium dioxide (TiO2) particles through a sol–gel (spin coating) route. Feature of TiO2 nanoparticles on microstructural behaviour is evaluated via scanning electron microscope and X-ray diffraction, and its optical properties like absorption & transmittance, optical band gap, and optical conductivity are studied. Including 9 wt% TiO2 in PVA film shows increased absorption peaks of 220–440 nm, and the transmittance range decreased by 16% compared to pure PVA. In addition, the optical energy band gap decreased from 3.7 to 2.6 eV, and its optical conductivity progressively increased from 0.1 to 1.3 × 1012. [ABSTRACT FROM AUTHOR]

The performance of cementitious composites reinforced with fibres or/and bars depends on the bond strength between inclusion and cementitious matrix. The nature of formation of fibre‐matrix bond is crucial for enhancing the reliability and utilisation of reinforced composites. The research provides a review on the recently published result about the changes in the microstructure of cement matrix surrounding steel fibres with different surface roughness, using a scanning electron microscope (SEM) coupled with k‐means clustering algorithm for image segmentation. The debonding pattern of the fibre‐matrix bond after the tensile loading cycles was discussed by observing the amount of adhered cement paste to the pulled out fibre surface with SEM. Therefore, analysis of SEM images enabled to explain the connection between the micro‐scale properties of cement paste and fibre after application of cyclic loading. [ABSTRACT FROM AUTHOR]

Unburned carbon from fly ash and its graphitization products (at temperatures of 2400 and 3000°C) were tested using scanning electron microscope (SEM), X-ray diffraction (×RD) and micro-Raman spectroscopy. The same tests were also carried out for synthetic and natural graphite. Various morphological forms of products with a high degree of graphitization, such as spheroidal graphite, hexagonal plates, column plates, and jagged-edge films were identified in the sample of unburned carbon annealed at 3000°C. The product of thermal treatment at the temperature of 3000°C has the interlayer spacing d002 value characteristic for semigraphite. With increasing temperature the number of crystallites in stack N, their height Lc002 and aromaticity fa increases. The degree of G graphitization of annealed samples increases more than twice with increasing temperature. With the increase of the temperature the aliphatic chains are decomposed and the aromatic systems are reconstructed, so the degree of internal structure order increases. The Raman examinations showed that the structural parameters determined for the graphite and carbonizate samples after thermal treatment at the temperature of 3000°C are equal in the standard deviation range. [ABSTRACT FROM AUTHOR]

To develop microwave‐absorbing properties of dielectric ceramics, B4C/C composite powders were prepared by combustion synthesis with B2O3, polyvinyl alcohol, and Mg as the raw materials in this work. The XRD, Raman, scanning electron microscope with energy‐dispersive spectroscopy, and VNA network analysis carried out the effects of the addition of azodicarbonamide (AC) foaming agent on the phase compositions, microstructure, and dielectric and microwave‐absorbing properties of the products. The results indicated that the addition of an AC foaming agent contributed to the formation of distinct morphologies with a larger specific surface area and uniform distribution of the free carbon in the B4C/C composite powders and improved its graphitization degree, which resulted in the formation of equivalent microcapacitors, enhanced interfacial polarization, improved conductive network, and leading to a low reflection loss (RL) and a broadened effective absorb bandwidth (EAB). Due to the dielectric loss as the dominant loss mechanism, C‐1.5 (1.5 wt.% AC foaming agent addition) exhibits the EAB of 3.02 GHz and the minimum RL (RLmin) of −22.90 dB at the thickness of 2.20 mm. [ABSTRACT FROM AUTHOR]

Using Camellia oleifera shell as raw materials to preparative SiC ceramics by warm‐press forming and sintering is proposed in this paper. Warm‐press forming before preparing for the C. oleifera shell‐based SiC ceramics is beneficial to obtain the internal uniform and suitable pore structure of the cylindrical sample. Thermogravimetric analysis with differential scanning calorimetry was applied to analyze the pyrolysis behavior of C. oleiefra shell and phenolic resin. The scanning electron microscope and X‐ray diffraction were used to investigate the properties of C. oleifera shell‐based SiC ceramics. Then, the response surface method was applied to establish a multivariate prediction model based on the process parameters of warm‐press forming. And the regression equations of porosity and bending strength of COS‐SiC are obtained. The result demonstrated that the predicted and experimental values can be in good agreement for the model. By comparing the F‐value, it is found that the forming temperature and pressure during the process of warm‐press forming have a more significant influence on the porosity and bending strength of SiC ceramics. The optimization process parameters were obtained as follows: forming temperature 153°C, pressure 35 MPa, and holding time 30 min. [ABSTRACT FROM AUTHOR]

PyC/BN multiphase interfacial phases were prepared on the surface of SiC fiber preform, then the near stoichiometric ratio SiC fiber reinforced SiC ceramic matrix composites were obtained by polymer impregnation and pyrolysis (PIP) process. The mechanical behavior of SiC/SiC composites was characterized by three‐point bending tests and fracture toughness tests. The stress release and load transfer effects of the interfaces under external loads were analyzed by scanning electron microscope (SEM). Results showed that with the increasing of PyC component thickness from.10 to.30 µm in the PyC/BN multiphase interfacial phases, the bending strength and fracture toughness both increased first and then decreased. The results occurred due to the competition between load transfer and stress release of the interfaces. The relatively optimized interfacial phase structure was that the thickness of the PyC interfacial phase and BN interfacial phase were.20 and.30 µm. The bending strength and fracture toughness of the optimized SiC/SiC composites reached 660.65 MPa and 29.01 MPa•m1/2. Respectively, many matrix cracks appeared in the horizontal and vertical directions, occupying almost the entire fracture section. The growth path of the matrix crack was significantly increased with many long fibers pulled out and broken, which was conducive to the strengthening and toughening of SiC/SiC composites. [ABSTRACT FROM AUTHOR]

In this work, microporous MgO–Al2O3 refractory aggregates were prepared with Mg(OH)2 and Al(OH)3 via the in situ decomposition synthesis method. The effect of Al(OH)3 addition on the microstructure and properties of microporous MgO–Al2O3 refractory aggregates was investigated with scanning electron microscope and mercury intrusion porosimetry. The results indicated that the improved green density of the samples and the reaction sintering accelerated the mass transport rate with adding Al(OH)3 from 0 to 4.0 wt%. Besides, a small amount of Al3+ diffused into porous MgO particles, accelerating the merging and growth of nanopores in the porous MgO particles. The intra‐particle pore size and the densification degree of microparticles were increased, and thus the strength of the samples was improved. Due to the formation of Kirkendall voids by interdiffusion of Mg2+ and Al3+, the inter‐particle pore size increased. Adding Al(OH)3 from 4.0 to 17.6 wt%, the Kirkendall voids weakened the mass transport rate and improved the inter‐particle pore size. The merging and growth of nanopores in the MgO particles were limited, resulting in the reduced intra‐particle pore size and increased intra‐particle pore number. The densification degree of microparticles was reduced, and thus the strength of the samples decreased. At the Al(OH)3 addition of 4.0 wt%, microporous MgO–Al2O3 refractory aggregates had the best comprehensive properties, a bulk density of 2.48 g/cm3, an apparent porosity of 29.4%, a median pore size of 1.6 μm with 42.2 vol% nanopores and the thermal conductivity of 4.0 W/(m K). [ABSTRACT FROM AUTHOR]