Scanning Electron Microscopy Methods Research Articles

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.

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.

Application of fucoidan for the encapsulation of yeast K2 toxin

Fucoidan is an anionic polysaccharide derived from brown algae and is composed of l-fucose residues linked by alternating α-(1→3) with α-(1→4) linkages or by either α-(1→3) or α-(1→4) linkages alone. Fucoidan is known for its pharmacological, antibacterial, and antifungal properties and is used in the food industry. The aim of the study was to apply fucoidan to the formulation of the yeast killer toxin K2 produced by Saccharomyces cerevisiae. K2 toxin-loaded fucoidan particles were formed by a low-cost complexation method. They were characterised by dynamic light scattering, FT-IR spectroscopy, and scanning electron microscopy methods. The particles ranged in size from 180 to 280 nm and were stable for at least one month at 4°C. The encapsulated K2 toxin retained its antimicrobial activity. In addition, complexation with fucoidan increased the stability of the K2 toxin at room temperature. Fucoidan could serve as a carrier for K2 toxin and enhance the biotechnological potential of antimicrobial agents produced by S. cerevisiae. Encapsulation of K2 toxin opens up opportunities for its use in the food and beverage industry for biopreservation.

Advanced Chemical and Imaging Methods for Studying Structure Morphology and Excipients Solid State Transformations in Pharmaceutical Multiparticulate Formulations

The formulation of paediatric medicines faces significant challenges to meet the requirements for safe and accurate administration, while maintaining a suitable taste. Multiparticulate formulations have a strong potential to address these challenges because they combine dose flexibility with ease of administration. Understanding the stability of multiparticulate formulations over storage as a function of time and environmental parameters, such as humidity and temperature, is important to manage their commercialisation and use. In this work, we have expanded the toolkit of available techniques for studying multiparticulates beyond those such as scanning electron microscopy (SEM) and confocal laser scanning microscopy. We include advanced methods of environmentally-controlled SEM to monitor temperature- and humidity-induced changes in-situ, and a variety of Raman spectroscopies including stimulated Raman scattering microscopy to identify and localise the different ingredients at the surface and inside the multiparticulates. These techniques allowed unprecedented monitoring of specific changes to the particulate structure and distribution of individual ingredients due to product aging. These methods should be considered as valuable novel tools for in-depth characterisation of multiparticulate formulations to further understand chemical changes occurring during their development, manufacturing and long-term storage. We envisage these techniques to be useful in furthering the development of future medicine formulations.

Synthesis and upconversion luminescence properties of Ho3+-Yb3+ co-doped glass ceramics containing LiGd(WO4)2

Ho3+-Yb3+ co-doped glass ceramics containing LiGd(WO4)2 were prepared by melt crystallization method. By using the methods of differential scanning calorimetry (DSC), X-ray diffraction (XRD), transmittance, and scanning electron microscopy (SEM), the optimal heat treatment condition for the samples was identified to be 580 °C/140 min. In these conditions, the transmittance of glass ceramic is about 75 % in the 380–780 nm range. In the upconversion emission spectra, strong green emission (543 nm) and red emission (650 nm) due to 5F4/5S2, 5F5→5I8 transitions are observed at 980 nm excitation. Additionally, the optimum doping concentrations of Ho3+ and Yb3+ were 0.12 % and 0.4 %. The crystal field changes around dopant ions were analyzed using J-O theory and Eu3+ probe to explain the up-conversion luminescence enhancement of glass ceramics containing LiGd(WO4)2. The chrominance coordinates of 0.12 % Ho3+-0.4 % Yb3+ co-doped glass ceramics are located in the green light region, and the color purity is 95.6 %. In summary, Ho3+-Yb3+ co-doped transparent glass ceramics containing LiGd(WO4)2 have potential applications in infrared detection and green solid-state lasers.

The Effect of W, Cr, Mo Content on the Microstructure and Mechanical Properties of the Weld Interface of TiC Cermet and Low-Carbon Steel

In this study, the influence of W, Cr, and Mo on the microstructure and mechanical properties of the arc-welded interface of TiC cermet and low-carbon steel was investigated. MIG arc welding was employed to deposit muti-alloyed low-carbon steel flux-cored wire onto the surface of the TiC cermet to create the arc-welded interface. Analysis of the microstructure, phase composition, and shear fracture of the interface were conducted by OM (optical microscopy), SEM (scanning electron microscope), EMPA (Electron Probe X-ray Micro-Analyzer), and XRD (X-ray diffraction) methods. The results indicate that the order of influence on the performance of the welded interface is perceived as Cr > W > Mo. The preferred ratio of element content is W at 1.0 wt.%, Cr at 0.5 wt.%, and Mo at 2.0 wt.%. During the arc-welding process, W and Mo formed a rim structure of TiC particles to inhibit the dissolution of TiC particles, while Cr formed dispersed carbides in the bonding phase. The synergistic impact of these components resulted in the simultaneous enhancement of both the TiC particles and the bonding phase. This led to a significant increase in the shear strength of the TiC cermet welded interface to 787 MPa, marking an 83% improvement compared to the welded interface without reinforcement, which exhibited a shear strength of 430 MPa.

Improving Tamoxifen Performance in Inducing Apoptosis and Hepatoprotection by Loading on a Dual Nanomagnetic Targeting System.

Although tamoxifen (TMX) belongs to selective estrogen receptor modulators (SERMs) and selectively binds to estrogen receptors, it affects other estrogen-producing tissues due to passive diffusion and non-differentiation of normal and cancerous cells and leads to side effects. The problems expressed about tamoxifen (TMX) encouraged us to design a new drug delivery system based on magnetic nanoparticles (MNPs) to simultaneously target two receptors on cancer cells through folic acid (FA) and hyaluronic acid (HA) groups. The mediator of binding of two targeting agents to MNPs is a polymer linker, including dopamine, polyethylene glycol, and terminal amine (DPN). Zeta potential, dynamic light scattering (DLS), and Field emission scanning electron microscopy (FESEM) methods confirmed that MNPs-DPN-HA-FA has a suitable size of ~105 nm and a surface charge of -41 mV, and therefore, it can be a suitable option for carrying TMX and increasing its solubility. The cytotoxic test showed that the highest concentration of MNPs-DPN-HA-FA-TMX decreased cell viability to about 11% after 72 h of exposure compared to the control. While the protective effect of modified MNPs on normal cells was evident, unlike tamoxifen, the survival rate of liver cells, even after 180 min of treatment, was not significantly different from the control group. The protective effect of MNPs was also confirmed by examining the amount of malondialdehyde, and no significant difference was observed in the amount of lipid peroxidation caused by modified MNPs compared to the control. Flow cytometry proved that TMX can induce apoptosis by targeting MNPs. Real-time PCR showed that the modified MNPs activated the intrinsic and extrinsic mitochondrial pathways of apoptosis, so the Bak1/Bclx ratio for MNPs-DPN-HA-FA-TMX and free TMX was 70.82 and 0.38, respectively. Also, the expression of the caspase-3 gene increased 430 times compared to the control. On the other hand, only TNF gene expression, which is responsible for metastasis in some tumors, was decreased by both free TMX and MNPs-DPN-HA-FA-TMX. Finally, molecular docking proved that MNPs-DPN-HA-FA-TMX could provide a very stable interaction with both CD44 and folate receptors, induce apoptosis in cancer cells, and reduce hepatotoxicity. All the results showed that MNPs-DPN-HA-FA-TMX can show good affinity to cancer cells using targeting agents and induce apoptosis in metastatic breast ductal carcinoma T-47D cell lines. Also, the protective effects of MNPs on hepatocytes are quite evident, and they can reduce the side effects of TMX.

Failure behavior and life prediction of solvent-free epoxy coatings based on impedance spectroscopy

The degradation process and electrochemical characteristics of an environment-friendly solvent-free epoxy coating in 3.5 % NaCl solution was investigated by using electrochemical impedance spectroscopic (EIS) studies. Combined with open circuit potential (OCP), adhesion tests, Fourier Transform Infrared Spectroscopy (FTIR) and Scanning Electron Microscopy (SEM) methods, the failure mechanism of the coating was analyzed. The results show that the failure of the coating is mainly caused by physical processes due to many nanoscale defects providing channels for the diffusion of corrosive media. The low-frequency impedance (|Z|0.01Hz) decreases to about 1 × 107 Ω cm2, demonstrating a poor protection performance of the coating, manifested by the coating adhesion decreasing about 50 %–60 % and corrosion products observed on the substrate by SEM. The mathematical formula proposed by Bierwagen is suitable for predicting the service life of the solvent-free epoxy coating combined with a suitable failure criterion.

One pot synthesis of amino silane grafted cerium phosphate (AS@CePO4) as an effective anticorrosion nanopigment for epoxy coating

This work proposed a facile method to synthesize an effective anticorrosion nanopigment based on amino silane grafted cerium phosphate for epoxy coated steel system. CePO4 nanoparticles were synthesized from Ce(NO3)3 and Na3PO4 precursors, then surface-grafted with a coupling agent N-2-(aminoethyl)-3-aminopropyl trimethoxysilane (denoted as AS) via a one-pot reaction to obtain the AS@CePO4 nanopigment. The effectiveness of this nanopigment on corrosion protection, dry/wet adhesion strength, and cathodic disbondment resistance was thoroughly evaluated on an epoxy-coated steel system. The composition and morphology of pigments as well as epoxy containing pigments were characterized by Fourier transform infrared spectroscopy (FT-IR), field emission scanning electron microscopy (FE-SEM) and X-ray diffraction (XRD) methods. The adhesion strength, cathodic disbondment resistance and corrosion protection performance characteristics of the coatings were evaluated by pull-off test, cathodic disbondment test, electrochemical and salt spray tests, respectively. The synergic effect from stronger bonding of AS coupling agent and excellent inhibitory ability of CePO4 led to strengthened adhesion strength, better corrosion protection performance, and higher cathodic disbondment resistance of epoxy coated steel system.

Assessment of Some Characteristics of a Novel Photocatalyst Based on Hydrotalcite Mg‐Al‐Ag, Titanium Dioxide and Magnetic Iron Nanoparticles

AbstractThe utilization of metals and metal oxides as photocatalysts is a common method for treating dye contamination. Titanium dioxide nanoparticles (TNPs) are well known for their effectiveness as a photocatalyst in ultraviolet regions, while the inclusion of silver nanoparticles (AgNPs) can improve the photocatalytic properties of the nanocomposite materials in visible light. However, the TNPs and AgNPs are difficult to collect for reuse in water treatment due to their limited dispersion. Henceforth, this work recommended a novel photocatalyst based on hydrotalcite Mg−Al, magnetic Fe3O4 nanoparticles (FNPs), AgNPs, and TNPs prepared using the co‐precipitation method. Additionally, organic silane was first time used as a coupling agent to combine the components together. Consequently, the obtained products were applied for the degradation of methylene blue (MB) under natural sunlight. The characteristics of the synthesized nanocomposites were determined using infrared spectroscopy, vibrating‐sample magnetometer, X‐ray diffraction, dynamic light scattering, and scanning electron microscopy methods. The degradability of MB under sunlight was investigated using ultraviolet‐visible method. Moreover, the antibacterial activity and cytotoxicity of these nanocomposites has been tested and discussed.

Rapidly solidified Al-Cu-Co quasicrystalline alloy: microstructure and catalytic properties

This study presents the characterisation and evaluation of the catalytic potential of an alloy with a composition referring to the quasicrystal from the Al-Cu-Co system. The material was synthesised through a melt-spinning process, providing rapid solidification conditions and a favourable material form of thin ribbons. Microstructural and chemical analyses were performed using scanning electron microscopy, X-ray diffraction and transmission electron microscopy methods. The obtained results confirmed the presence of a major phase which was a decagonal quasicrystal in the form of globular grains and additional crystalline phases occurring along the grain boundaries. The catalytic potential of the materials was explored using phenylacetylene hydrogenation. The catalyst, obtained by pulverising the ribbons, demonstrated catalytic activity with over 40% phenylacetylene conversion and selectivity exceeding 60% for styrene production under mild reaction conditions. The recovered catalyst displayed a stable phase composition, as confirmed by X-ray diffraction, and unchanged morphology, indicating the possibility of catalyst reuse for subsequent reaction cycles. The presented results provide insight into the experimental verification of the catalytic properties of the developed environmentally friendly catalysts.