Scanning Electron Microscopy Methods Research Articles

A Nafion/BiVO4-COOH-MWCNTs/GCE for the sensitive determination of Cd2+ and Pb2+ by DPASV

BiVO4 was hydrothermally prepared and then ultrasonically mixed with carboxylated multiwalled carbon nanotubes (COOH-MWCNTs) to yield a BiVO4-COOH-MWCNTs composite. The composite were cast-coated on a glassy carbon electrode (GCE) to yield a BiVO4-COOH-MWCNTs/GCE, and then a Nafion solution was cast-coated on the BiVO4-COOH-MWCNTs/GCE to yield a Nafion/BiVO4-COOH-MWCNTs/GCE. The related materials and electrodes were characterized by field emission scanning electron microscopy, X-ray diffractometer and electrochemical methods. Under the optimal experimental conditions, Cd2+ and Pb2+ were analyzed by differential pulse anodic stripping voltammetry on the Nafion/BiVO4-COOH-MWCNTs/GCE, giving a linear detection range (LDR) from 10.0 nM to 2.00 μM and a limit of detection (LOD, S/N = 3) of 0.5 nM for Cd2+, as well as a LDR from 10.0 nM to 1.00 μM and a LOD of 0.9 nM for Pb2+. The Nafion/BiVO4-COOH-MWCNTs/GCE exhibited good selectivity, stability and reproducibility and returned satisfactory results of determining Cd2+ and Pb2+ in seafood samples.

Endohelminth diversity in the invasive Clarias gariepinus (Burchell, 1822) from two freshwater lakes: Naivasha and Ol'Bolossat, Kenya.

Fish parasitology contributes to our understanding of the potential risks posed by diverse groups of parasitic organisms on fish stocks in either wild and culture systems. This study was conducted in May 2023 and aimed at assessing the diversity of endohelminths in the invasive North African catfish Clarias gariepinus (Burchell, 1822) obtained from two freshwater lakes, Naivasha and Ol'Bolossat, in Kenya. Parasitological examination of 66 and 35 fish samples collected from the two lakes respectively was achieved using light and scanning electron microscopy methods. Results revealed endohelminth diversity broadly classified as four digeneans, two nematodes, and one cestode. Seven taxa of endohelminths were found in C. gariepinus samples, but only four of these taxa could be identified up to the species level. Six of the taxa (Diplostomum sp., Tylodelphys mashonense, Plagiorchioidea sp., Paracamallanus cyathopharynx, Contracaecum sp., and Tetracampos ciliotheca) were common in samples from the two lakes. Glossidium pedatum only occurred in samples from Lake Ol'Bolossat. Parasite prevalence ranged from 8.6 (T. mashonense) to 100% (Diplostomum sp., T. ciliotheca, and Contracaecum sp.) and mean intensity from 1.4 (T. mashonense) to 16.9 (Diplostomum sp.). The diversity and richness indices were comparatively higher in fish samples from Lake Ol'Bolossat and attributed to the occurrence of G. pedatum in the Ol'Bolossat. However, parasitic infestation of fish samples from the two lakes depicted close similarity, both in diversity and prevalence. These findings form an important baseline data for further follow-up studies, and they suggest the need for further molecular analyses to fully describe three of the taxa only identified up to the genus level.

A Study on the Surface Oxidation Pretreatment and Nickel Plating Mechanism of Carbon Fiber

This study explores the effects of various temperatures on the surface modification of carbon fibers, as well as the effect of differing voltages and currents on the morphology, deposition rate, and thickness of the Ni plating layers. Post-treatment characterization of the samples was conducted utilizing scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS) methods, thus facilitating a discussion on the mechanism of Ni plating. The findings demonstrate that at a temperature of 500 °C, the carbon fiber surface exhibits the highest concentration of functional groups, including hydroxyl (-OH), carboxyl (-COOH), and carbonyl (-C=O), resulting in the most efficacious modification. Specifically, exceeding 500 °C leads to significant carbon fiber mass loss, compromising the reinforcement effect. Under a stable voltage of 7.5 V, the Ni-plated layer on the carbon fibers appear smooth, fine, uniform, and complete. Conversely, at a voltage of 15 V, the instantaneous high voltage induces the continuous growth of Ni2+ ions along a singular deposition point, forming a spherical Ni-plated layer. In addition, a current of 0.6 A yields a comparatively uniform and dense carbon fiber coating. Nickel-plated layers on a carbon fiber surface with different morphologies have certain innovative significance for the structural design of composite reinforcements.

Electron Beam Interaction with Carbon Nanotubes in Scanning Electron Microscope: Mechanisms and Applications

AbstractA comprehensive understanding of the interaction between electron beams and carbon nanotubes (CNTs) in scanning electron microscope (SEM) can be challenging due to the complex surface charging behavior and various nanostructures formed by CNTs. Herein, an overview of the challenges and potential solutions are provided for achieving high‐resolution imaging of nanomaterials, such as CNTs, in SEM systems. First, imaging mechanisms of CNTs on conducting, insulating, and hybrid substrates are summarized, with morphology, material type, and charging effect covered. Second, measuring the conductivity, bandgap, and diameter of a CNT by SEM method is introduced. Finally, the utilization of super‐aligned CNT (SACNT) films for observing insulators and vertically aligned CNT arrays (VACNTAs) as electron blackbodies are discussed separately. New techniques for imaging and characterizing nanostructures will ultimately lead to the advancement of CNT‐based technologies.

Application of digital image correlation for in-situ deformation studies using transmission electron microscopy

Digital Image correlation (DIC) is routinely applied using optical and scanning electron microscopy methods to map local strains during deformation. In this letter, we report its use for in-situ TEM imaged deformation evolution for a nanocrystalline metal. Since transmitted electrons give rise to complex contrast conditions, with such contrast associated with the mechanisms of deformation, one can track these changes if particular care is done in image analysis and interpretation. We describe these methodologies to enable this correlation through frame averaging. Using these collective correlation conditions, we found that the average DIC strain matches well with the far field strain values yielding increased confidence in its application. Through the utilization of DIC in the TEM, nanoscale deformation mechanisms can be further elucidated because of the increased spatial resolution offered by TEM.

Understanding of the correlation of structural and microwave dielectric performance of (1-x)MgTiO3 - xCaTiO3 ceramics for dielectric resonator antenna applications

In this article, the effect of CaTiO3 on the structural and microwave dielectric characteristics of MgTiO3 has been discussed. The (1-x)MgTiO3 - xCaTiO3 (abbreviated as (1-x)MT- xCT) for x = 0.025, 0.05, 0.075, 0.1 ceramics have been developed using a solid-state reaction route. The structural as well as morphological characteristics of specimens have been observed by employing X-ray diffraction and scanning electron microscope methods. The Rietveld refinement technique of X-ray diffraction data have been conducted for the refinement of structural phases. It suggests that two crystallographic phases have been present in all materials. The SEM images display dense well-identified grains of (1-x)MT - xCT (for x = 0.025 - 0.1) ceramics. The Raman spectroscopy method has been employed to detect the symmetry of ceramics and modes of vibration of the materials. The microwave dielectric characteristics like dielectric permittivity (εr), loss (tanδ), quality factor (Q×f), and temperature coefficient at resonant frequency (τf) of (1-x)MT - xCT (for x = 0.025 - 0.1) ceramics have been thoroughly investigated. The bond strength, bond valency, bond energy, and tolerance factor of (1-x)MT - xCT (for x = 0.025 - 0.1) materials have been evaluated and their relation with microwave dielectric characteristics has been discussed. The (1-x)MT - xCT (for x = 0.025 - 0.1) ceramics show excellent dielectric properties with near to zero τf. In addition, DRAs have been designed with (1-x)MT - xCT (for x = 0.025 - 0.1) materials as dielectric resonators and various antenna properties have been studied with the help of HFSS software. This work suggests that (1-x)MT - xCT for (x=0.05) material can be a promising candidate for DRA applications working in the C band.

In vitro and in silico studies of the inclusion complexation of 8-bromobaicalein with β-cyclodextrins

Baicalein, a flavone derived from Scutellaria baicalensis Georgi, exhibits potent anti-inflammatory, antiviral, and anticancer properties. Its derivative, known as 8-bromobaicalein (BB), has been found to have strong cytotoxic properties against MCF-7 human breast cancer cells. However, its limited solubility in water has hindered its potential for wider applications. To address this issue, we investigated the use of cyclodextrins specifically βCD, 2,6-di-O-methyl-β-cyclodextrin (DMβCD), and hydroxypropyl-β-cyclodextrin (HPβCD) to improve the solubility of BB through inclusion complexation. During 250 ns molecular dynamics simulations, it was found that BB can form inclusion complexes with all βCDs. These complexes exhibit two distinct orientations: chromone group insertion (C-form) and phenyl group insertion (P-form). The formation of these complexes is primarily driven by van der Waals interactions. DMβCD has the highest number of atom contacts with BB and the lowest solvent accessibility in the hydrophobic cavity. These results coincide with the highest binding affinity from the MM/GBSA-based free energy calculation method. Experimental phase solubility diagrams revealed a 1:1 stoichiometric ratio (AL type) between BB and βCDs, in which BB/DMβCD showed the highest stability. The formation of inclusion complexes was confirmed by differential scanning calorimetry and scanning electron microscope methods. Additionally, the BB/DMβCD inclusion complex demonstrated significantly higher anticancer activity against MCF-7 human breast cancer cells compared to BB alone. These findings underscore the potential of DMβCD for formulating BB in pharmaceutical and medical applications.

Scratching of metallized polymer films by Vickers indenter as a method for controlled production of SERS-active metasurfaces

The potentialies of a system of parallel microscratches drowed on a PET film metallized with silver and copper using a Vickers indenter as an active Surface-enhanced Raman spectroscopy (SERS) surface have been investigated. It is shown that the magnification of the SERS signal for rhodomine is proportional to the total length of microscratches in the laser spot and increases after their application due to the relaxation of the polymer backing. The results of the microscratch geometry analysis by an atomic force microscopy and scanning electron microscopy methods indicate the probability of the location of "hot points" along the "dumps" of metal along the shores of scratches, as well as on nanoroughnesses along their inner walls.© 2017 Elsevier Inc. All rights reserved.

Laser synthesis of oxide nanoparticles with controlled gas condensation

In this work, the oxide nanopowders of Al2O3, ZrO2, Y2O3, Gd2O3, CeO2, and SiO2 were synthesized by CW CO2 laser vaporization technique with controlled gas condensation in an inert atmosphere. Methods for controlling the size of the resulting nanoparticles by adjusting the gas composition and pressure during the vaporization process have been demonstrated. The potential for producing ultrasmall oxide nanoparticles with dimensions less than 5 nm has been shown. The size distribution of nanoparticles taken from different parts of the evaporation-condensation tract was studied using scanning (SEM) and transmission (TEM) electron microscopy methods. The effect of synthesis conditions (pressure and composition of the inert gas) on characteristics of the nanoparticles is discussed. Using a wide class of simple oxides as the example, it is shown that the powders synthesized by the laser method consist of three types of particles: target spherical particles with a diameter of 3–20 nm (more than 98%), larger spherical particles with a diameter of 50–200 nm, and shapeless large particles with sizes more than 200 nm. The possibility of separating large particles from the main particles using the original labyrinth system for gas pumping is shown. The obtained particles with controlled sizes can be effectively used in various applications, in particular, for the preparation of catalysts and adsorbents.

Влияние режимов лазерной наплавки на геометрические размеры стального трека

Introduction. Laser surfacing is one of the leading trends in the field of additive technologies, which consists in layer-by-layer build of material using a laser as an energy source. To obtain a high-quality product, it is necessary to select the optimal building parameters correctly. The problem is that such optimization is necessary for all equipment, since minor differences in its characteristics can make significant changes in the parameters of layer-by-layer build. In order to determine the optimal build mode, it is enough to analyze the effect of various equipment parameters on the characteristics of single tracks. Therefore, the purpose of this work is to determine the most important parameters of laser radiation that affect the surfacing process and the optimal mode for building a single track of chromium-nickel steel. The work investigated single tracks obtained by laser surfacing of powder from austenitic chromium-nickel steel AISI 316L. The optimization factors included such characteristics as laser power, beam speed, flow rate of supplied powder and laser spot size. The wavelength of laser radiation was 1.07 μm. Research methods. To determine the quality and geometric dimensions of single tracks, the macrostructure of cross sections of specimens was studied using metallography and scanning electron microscopy methods. Results and discussion. It is established that the optimal mode for growing single tracks of steel AISI 316L is characterized by a laser radiation power of 1,250 W and a scanning speed of 25 mm/s. In this case, the optimal powder consumption rate is 12 g/min, and the laser spot size is 4.1 mm. The work shows that the powder consumption and laser spot size have the greatest influence on the coefficient of effective use of powder material. By changing it, the surfacing performance can be increased by 10–15 %.

Developing a new ethylene glycol/H2O pretreatment system to achieve efficient enzymatic hydrolysis of sugarcane bagasse cellulose and recover highly active lignin: Countercurrent extraction

Improving pretreatment efficiency is a critical premise in achieving efficient biomass conversion, and obtaining high-performance natural polymers is the guarantee of high-value conversion of biomass. In this study, a new pilot-scale continuous countercurrent pretreatment reaction unit about ethylene glycol-alkali solution was designed for pretreating sugarcane bagasse in order to achieve efficient separation of the three major components of lignocellulose when expanding the scale of pretreatment, reduce lignin deposition on the fiber surface, and obtain highly active lignin and excellent enzymatic hydrolysis efficiency of cellulose. X-ray diffractometer (XRD), X-ray photoelectron spectrometer (XPS), brunauer-emmett-teller (BET) and scanning electron microscope (SEM) methods are used to analyze the structural properties of sugarcane bagasse before and after pretreatment, and high-performance liquid chromatography (HPLC) is used to analyze the monosaccharide components in the enzymatic solution. In addition, the structural properties of the recovered lignin are analyzed by gel permeation chromatography (GPC), 31P NMR and 2D-HSQC-NMR methods. The results indicate that the system can gain a high cellulose recovery of 92.99 % along with a lignin removal of 95.33 %, and recovered lignin has low lignin carbohydrate complexes, low condensation, and rich in phenolic hydroxyl groups for 1.95 mmol/g. Meanwhile, the countercurrent pretreatment system can effectively reduce the deposition of lignin on the cellulose surface, which is evidently superior to the non-countercurrent pretreatment and facilitates the efficiency of enzymatic saccharification of substrate, achieving a high glucose yield of 99% as well as a total sugar yield of 91.11 %. The method efficiently separates biomass in a green manner, and solid residues are easily hydrolyzed, showing potential for industrial-scale production.

Novel MAXPOWER biological antibacterial liquid for eradicating oral Helicobacter pylori

BackgroundEradication of oral Helicobacter pylori (H. pylori) not only reduces the infection rate from the transmission route but also improves the success rate of intragastric eradication. MAXPOWER Biological Bacteriostatic Liquid, developed in our previous work, is a composite biological preparation with strong antibacterial ability and unique antibacterial mechanism. The present study evaluated the efficacy of the MAXPOWER biocontrol solution on H. pylori and its success rate in eradicating oral H. pylori in clinical patients.MethodsLive-dead cell staining and hemolysis test were used to evaluate the cellular safety of MAXPOWER biocontrol solution; plate spreading, live-dead bacterial staining, and scanning electron microscopy methods were used to evaluate its antimicrobial effect against H. pylori. Transcriptomics was used to analyze the changes in H. pylori genes before and after treatment. After seven days of gavage treatment, H&E staining and mice feces were collected for 16SrDNA sequencing to evaluate the animals’ safety. Oral H. pylori-positive patients were randomized to be given a placebo and MAXPOWER Bio-Bacteriostatic Liquid gargle for seven days to evaluate the effect on oral H. pylori eradication.ResultsIn vitro tests demonstrated that this product has excellent biocompatibility and hemocompatibility and can effectively eradicate oral H. pylori. In vivo tests further showed that it has good biosafety and virtually no adverse effect on intestinal microflora. Transcriptomics analysis revealed that it kills H. pylori cells mainly by disrupting their cell membranes and metabolism. Additionally, the results of randomized controlled trials on humans disclosed that the oral H. pylori eradication rates achieved by MAXPOWER Biological Antibacterial Liquid were 71.4% and 78.9% according to the intention-to-treat and the per-protocol analysis, respectively.ConclusionMAXPOWER Biological Antibacterial Liquid is both safe and efficacious in the eradication of oral H. pylori.Trial registrationThis study was retrospectively registered in the ClinicalTrials.gov Trial Registry on 21/09/2023 (NCT06045832).

Synthesis and study of organo-modified silica based hydrogels: Rheological properties and drug release kinetics.

The method of synthesis of unmodified and organo-modified silica hydrogels and their composites with orotic acid as a model drug was developed. The hydrogels had a pH of 6.5-7.8. The particulate nature and highly porous structures of the hydrogel materials were revealed using scanning electron and optical microscopy methods. The content of aqueous phase in the hydrogels was 99% or more. In order to evaluate the possibility of their application as a basis for development of novel soft drug formulations and cosmetic compositions, rheological properties of the hydrogels and in vitro release kinetics of the drug were studied. The effects of synthesis conditions (increasing concentration of catalyst of silica sol formation, drug loading) and the silica matrix modification with various organic groups on the indicated properties were investigated. It was found that all synthesized hydrogels exhibited pseudoplasticity, thixotropy and controlled release of the drug, which are important for their potential application. However, in general, the indicated effects led to worsening the properties of the hydrogel materials in comparison with the unmodified silica hydrogels.

Effects of Mn and Ru substitutions on the electrical properties and AC susceptibility of Tl(BaSr)CaCu2O7 superconductor

In this paper, the effects of M = Mn and Ru substitutions at the Tl site of Tl[Formula: see text]Mx(BaSr)CaCu2O7 (Tl-1212) on the electrical properties and AC susceptibility were investigated. The X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM) methods were used to examine the phase and microstructure, respectively. All samples showed diffraction patterns with Tl-1212 as the major phase and an increase in the Tl-1223 phase with increasing Mn and Ru substitutions. The microstructure showed partial melting and randomly oriented grains in all samples. The electrical resistance measurements showed metallic normal state behavior for all samples. The zero-resistance transition temperature [Formula: see text] was the highest for x = 0.4 where [Formula: see text] was 107[Formula: see text]K and 90[Formula: see text]K for Mn and Ru substitutions, respectively. The superconducting transition, [Formula: see text] obtained from AC susceptibility measurements increased with Mn and Ru substitutions up to x = 0.4. Using Bean’s model, the current density at the peak temperature of the imaginary part of the AC susceptibility, [Formula: see text]([Formula: see text] was determined to be between 16 and 22[Formula: see text]A[Formula: see text]⋅[Formula: see text]cm[Formula: see text] for Mn, and between 15 and 19[Formula: see text]A[Formula: see text]⋅[Formula: see text]cm[Formula: see text] for Ru-substituted samples. Mn substitution showed a higher transition temperature compared with Ru. This study showed that optimization of the average Cu valence was achieved with Mn and Ru substitutions for x = 0.4 at the Tl site. The ionic radii of the substituting and substituted elements are important factors in enhancing the transition temperature of Tl(BaSr)CaCu2O7 superconductor.

Comparative physicochemical investigation of the inclusion compounds of cyclodextrins with arginine and histidine stereoisomers

The inclusion complexes of α-, β-cyclodextrin and 2-hydroxypropyl-α-cyclodextrin with two amino acid stereoisomers (L-, D-arginine and L-, D-histidine) were studied by using differential scanning calorimetry, thermogravimetry, Fourier transform infrared spectroscopy, and scanning electron microscopy methods. The solid inclusion compounds were prepared in a 1:1 molar ratio of the host and guest using the co-precipitation method. The pH measurements and structural visualization of complexes were carried out. The obtained results proved the formation of the complexes and revealed that the size and the symmetry of the cyclodextrin (CD) and also the structure and flexibility of the amino acid molecule had a significant influence on the complexation interaction. The correlation of the experimental data shows that βCD has a preference to form more stable complexes with levogir isomers of amino acid than αCD and 2-hydroxypropyl-α-cyclodextrin. The complexation of the amino acids isomers was accomplished by partial inclusion of the guest molecule in the CD cavity, and it was observed that CDs could better discriminate between histidine isomers than between arginine isomers.

Enhancing microstructure and mechanical properties of dissimilar TIG welded duplex 2205 and Ni-based inconel 718 superalloy through post weld heat treatment

In demanding applications, maintaining structural integrity in dissimilar welded joints like those between duplex stainless steel and Ni-based superalloys requires achieving the best possible mechanical properties. This work examines the impact of post-weld heat treatment (PWHT) on the mechanical characteristics of joints made via double-sided tungsten inert gas (TIG) welding. The dissimilar welded joint was investigated by exposing it to the PWHT for 12 h at 650 °C. Reducing the negative impact of heat generated by welding on the mechanical characteristics and microstructure of the fusion zone was the main goal. To study for changes in the microstructure before and after PWHT, optical microscopy and scanning electron microscopy methods were used for microstructural analysis. To determine the effect of PWHT on the welded joints, mechanical properties such as tensile strength, toughness, and ductility were also assessed. The mechanical properties showed significantly enhanced characteristics and refined grain structures in the fusion zone.

Luminescence properties of SrB6O10:Ce,Gd phosphor for applications in OSL dosimetry and lighting

Strontium hexaborate (SrB6O10) doped with different metals and/or lanthanides has been studied widely as the thermoluminescence (TL) dosimeter. However, there is almost no dosimetry study concerning the utility of Optically Stimulated Luminescence (OSL) on SrB6O10. This preliminary study aims to examine the luminescence properties of SrB6O10 phosphor for their application in the areas of dosimetry and lighting technologies. Undoped and doped material to get an OSL dosimeter were synthesized by incorporating the dopants Ce3+, in the range of 0.1–0.7 % wt, and Gd3+, in the range of 0.1–1 % wt into the SrB6O10 structure using the solution combustion (SCS) method. The structural and morphological characterizations were performed using X-ray diffraction (XRD) and Scanning Electron Microscope (SEM) methods, respectively. Two TL peaks of SrB6O10:Ce0.1%,Gd0.5% occurred at 70 °C and 182 °C after 1 Gy exposure to beta rays with a heating rate of 2 °C/s. The step annealing measurements were carried out to determine the traps responsible for the OSL signal. Various properties of the luminophore including dose-response and reusability were investigated using blue light stimulation. The phosphor showed a little variation of response up to 20 cycles within 2 % deviation (STD) from the first OSL readout. The OSL output within the range of 2–20 Gy was determined as linear. Radioluminescence (RL) measurement was investigated by emission in the range λem = 200–1000 nm. The parent compound displayed UV emission subdivided into UVA (315–400 nm), and UVB (280–315 nm) emissions at room temperature. The Chromaticity Coordinates (CIE) of SrB6O10:Ce0.1%,Gd0.5% were calculated as x = 0.2165, y = 0.1767. These remarkable characteristics show that, if developed, SrB6O10 could be used as an OSL dosimeter.

Thermomechanical evaluation of zinc oxide/hydroxyapatite/high‐density polyethylene hybrid composites

AbstractThis study examines the impact of zinc oxide (ZnO) on the spectral, thermal, mechanical, and morphological characteristics of developed composites of high‐density polyethylene (HDPE). Composite samples were fabricated with different compositions of ZnO (0, 5, 10, 15, and 20 wt%) along with a constant quantity of hydroxyapatite (HA, 10 wt%) in pure HDPE. The synthesized hybrid polymer composites were characterized using Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), universal testing machine (UTM), and field emission scanning electron microscopy (FESEM) methods, allowing for a thorough assessment of their spectral, thermal, mechanical, and morphological properties, repectively. FTIR analysis revealed the presence of HA and ZnO metal vibrations in the hybrid polymer samples. The thermal stability was increased by the incorporation of different amounts of ZnO, and the decomposition temperature was increased from 319.31 to 412°C for 10 wt% of ZnO hybrid composites as compared to pure HDPE. DSC findings indicated that increasing the ZnO contents, prompted the degree of crystallinity to rise to 14.81% as contrasted to neat HDPE. It was observed that yield strength and ultimate tensile strength for the 10 wt% ZnO composite increased up to 51.85% and 31.72%, respectively, compared to pure HDPE. However, at higher loading of ZnO, surface cracks were observed, which is detrimental for composite materials. Hence, the improved attributes indicated that the synthesized ZnO/HA/HDPE polymer composites can be a promising material for biomedical engineering applications.

Durability of concrete-encapsulated GFRP bars subjected to seawater immersion

Glass fiber reinforce polymer (GFRP) bars have better durability than traditional steel bars, but there are few studies on their long-term performance in actual service environments especially the marine environment. To investigate the durability of GFRP bars used in cross-sea bridges, this research delves into the performance of 132 such bars, spanning diameters of 10, 12, 16, and 25 mm, in an environment that closely mimics real-world condition. The GFRP bars, encapsulated in concrete, were submerged in seawater solution, maintained at either room temperature or 60°C, for periods spanning from 0 to 183 days. Then the tensile strength and elastic modulus degradation of GFRP bars were investigated by tensile tests. Scanning electron microscope (SEM) was also used to analyze the micro-degradation mechanism of GFRP bars. In addition, this paper compares the four existing models for predicting long-term mechanical properties of GFRP bars with the experimental data, so as to determine the formulas and methods to be used in the design. The result shows that the elastic modulus of GFRP bars after 183 days of immersion in concrete pore solution was almost unchanged while the tensile strength decreased significantly. Among them, the tensile strength of 10 mm diameter GFRP bars decreased by 41.52 %, after 183 days of immersion at high temperature (60°C). The SEM method revealed that the main cause of such phenomena was the weakening of the bond between the fibers and matrix, which led to a decrease in the interface property. Finally, by fitting and comparing the relationship between the test data and the existing prediction models for the long-term mechanical properties of GFRP bars, the residual tensile strength of GFRP bars used in the actual project of Yanzhou Bridge for 100 years was predicted according to the optimal prediction model, i.e. the Serb model, and the results showed that the residual strength of GFRP bars is able to meet the current standard requirement.

Evaluating Bacterial Spore Preparation Methods for Scanning Electron Microscopy.

Scanning electron microscopy (SEM) can reveal the ultrastructure of bacterial spores, including morphology, surface features, texture, spore damage, germination, and appendages. Understanding these features can provide a basis for adherence, how physical and environmental stressors affect spore viability, integrity, and functionality, as well as the distribution and function of surface appendages. However, the spore sample preparation method can significantly impact the SEM images' appearance, resolution, and overall quality. In this study, we compare different spore preparation methods to identify optimal approaches for preparation time, spore appearance and resolved features, including the exosporium and spore pili, for SEM imaging. We use Bacillus paranthracis as model species and evaluate the efficacy of preparation protocols using different fixation and drying methods, as well as imaging under room- and cryogenic temperatures. We compare and assess method complexity to the visibility of the spore exosporium and spore appendages across different methods. Additionally, we use Haralick texture features to quantify the differences in spore surface appearance and determine the most suitable method for preserving spore structures and surface features during SEM evaluation. The findings from this study will help establish protocols for preparing bacterial spores for SEM and facilitating accurate and reliable analysis of spores' characteristics.