Scanning Electron Microscopy Methods Research Articles

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.

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.

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.

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 200 such bars, spanning diameters of 10, 12, 16, and 25mm, in an environment that closely mimics real-world conditions. The GFRP bars, encapsulated in concrete, were submerged in seawater solutions, 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 elastic modulus and tensile strength of 10mm diameter GFRP bars decreased by 5% and 35%, respectively, after 183 days of immersion at high temperatures (60°C). The SEM method revealed that the main cause of such phenomena was the weakening of the bond between the fibers and the matrix, which led to a decrease in the interface properties. 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 Bank model, and the results showed that the residual strength of GFRP bars is able to meet the current standard requirements.

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.

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.

Enhancing biocompatibility and osseointegration of medical implants using ti based nanocomposite coatings

The surface of the replacement medical implant can be coated, which is one of the most basic and effective ways to develop and strengthen bones and increase their compatibility for the human body to solve problems with bone defects, such as the problem of releasing ions from some elements of the body Medical alloy implants are one of the major drawbacks in bone fracture surgery, and biocompatible implants are new ways to ensure that these implants work well. These implants play a major role in accelerating osseointegration processes, but at the same time they suffer from the problem of releasing niobium and zirconium ions, which may cause serious diseases to human health. To stop these toxic ions from releasing, a bioceramic nanolayer coating was put on the alloy's surface. This made it more biocompatible and stopped the toxic ions from escaping. Among several types of coatings, the best nanocomposite coating was selected. Three criteria and levels were used: voltage, time, and cocentartion. A Takeuchi statistical program was used to collect data on all the tests (thickness, adhesion, contact angle, and roughness) in order to find the best coated sample. The study then used atomic force microscopy (AFM) and field emission scanning electron microscopy (FE-SEM) methods.

Electrochemical Deposition and Properties of Ni Coatings with Nitrogen-Modified Graphene Oxide

In this study, a method for producing nitrogen-modified graphene oxide (NMGO) using hydrothermal synthesis in the presence of triethanolamine is presented. The composition and structure of NMGO are characterized using X-ray phase analysis (XPA), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy, and Raman spectroscopy. Ni-based metal matrix coatings (MMCs) modified with NMGO were obtained from a sulfate-chloride electrolyte in the galvanostatic mode. The process of electrochemical deposition of these coatings was studied using chronovoltammetry. The microstructure of Ni–NMGO MMCs was studied using the XPA and SEM methods. It has been established that the addition of NMGO particles into the Ni matrix results in an increase in the microhardness of the resulting coatings by an average of 1.30 times. This effect is a consequence of the refinement of crystallites and high mechanical properties of NMGO phase. The corrosion-electrochemical behavior of studied electrochemical deposits in 0.5 M sulfuric acid was analyzed. It has been shown that the corrosion rate of Ni–NMGO MMCs in a 3.5% sodium chloride environment decreases by approximately 1.50–1.70 times as compared to unmodified Ni coatings. This is due to NMGO particles that act as a barrier preventing the propagation of the corrosion and form corrosive galvanic microelements with Ni, promoting anodic polarization.

WO3/ZnWO4 microcomposites with potential application in photocatalysis

The paper presents the results of a comprehensive study of the structural, optical and strength features, changes in the morphology of grains of (1-x)WO3 – xZnO ceramics depending on the concentration of the initial components when they vary. Using the X-ray diffraction method, it was found that mechanochemical grinding of samples of (1-x)WO3 – xZnO ceramics, regardless of the concentration of the components, does not lead to the initiation of phase transformation processes associated with the formation of the monoclinic ZnWO4 phase, the formation of which is observed during thermal annealing of samples at a temperature of 1000 °C. Based on data obtained using scanning electron microscopy and X-ray diffraction methods, the dynamics of phase transformations in ceramics of the type WO3/ZnWO4 → ZnWO4 → ZnO/ZnWO4 was established. It was found that with a given ratio of WO3: ZnO components equal to 0.7 : 0.3, under selected conditions of mechanochemical grinding and an annealing temperature of 1000 °C, highly ordered single-phase ZnWO4 ceramics with a wolframite structure can be obtained. Analysis of the optical characteristics and changes in the band gap depending on the ratio of the components showed a direct dependence of changes in the band gap on the phase composition of the ceramics. An assessment of the strength characteristics made it possible to establish that the formation of two-phase WO3/ZnWO4 ceramics leads to strengthening of the surface layer, while for two-phase ZnO/ZnWO4 ceramics a decrease in hardness is observed, the decrease of which directly correlates with changes in the content of the ZnO phase in the composition of the ceramics.

Specific surface area and microstructure of the surface of soil solid substrates of different genesis

The sorption characteristics of sand, peat, the arable layer of Moscow urbanozem and a mixture of these substrates were studied in conjunction with the surface topography of their solid phase, studied by scanning electron microscopy (SEM). The arable layer has the greatest ability to absorb nitrogen, and the peat substrate showed very low values of the sorbed gas. A different picture of the mutual arrangement of substrate sorption isotherms is observed when water vapour is used as a sorbing gas. Peat is distinguished by high values of sorbed moisture in the entire studied range of relative humidity. This leads to differences in the ranking of substrates by specific surface area in descending order of its values. So, the specific surface area by water sorption in the series: peat / arable layer / mixture / sand was: 420 / 72 / 45 / 4 m2/g, respectively. The given surface was ranked according to nitrogen sorption in a different sequence: 8.31 / 2.41 / 1.45 / 0.55 for the series: arable layer, mixture, peat and sand, respectively. The analysis of microstructural characteristics by the SEM method at various magnifications revealed the most developed, rough surface in the arable layer. It turned out to be geometrically the most diverse, even at magnification of ×20 000. The variety and heterogeneity of the relief of the interface of the phases leads to the appearance of hysteresis of the sorption/desorption curves. Its severity in the range of nitrogen vapor concentration in which hysteresis is detected, and in the maximum width of the hysteresis loop, also turned out to be the most significant in the arable layer. The very low nitrogen specific surface of peat, which is close to a sandy substrate, is associated with the presence of organic films draping and leveling the surface of peat particles, which was revealed by analyzing images obtained by scanning electron microscopy. The sorption of water showed their high hydrophilicity, which led to high values of substrate humidity in the entire studied range of relative humidity.

“Exploring the Inhibitory Potential of Acetoxime-Zinc Chloride Adduct in Saline Environments for Mild Steel Corrosion Protection”

ABSTRACT In this work, acetoxime, zinc chloride and acetoxime adduct of zinc chloride, [ZnCl2.2{HON=C(CH3)2}] (ZA) were investigated as corrosion inhibitor's in 3.5%NaCl solution on mild steel. The electrochemical analysis was carried out using polarization measurements and electrochemical impedance technique and surface analysis was done by Scanning electron microscope coupled with Energy-dispersive X-ray spectroscopy. Using surface analysis and electrochemical data it was concluded that an inhibition synergy was developed when ZA was taken instead of acetoxime or zinc chloride alone in solution phase. Scanning electron microscope methods were used to examine the samples surface in the presence of inhibited solutions. The efficiency of inhibition increases with the increasing concentration and attained the values of 97.18% for the 3mM concentration of ZA.

Cathodoluminescence differentiates sedimentary organic matter types

High-resolution scanning electron microscopy (SEM) visualization of sedimentary organic matter is widely utilized in the geosciences for evaluating microscale rock properties relevant to depositional environment, diagenesis, and the processes of fluid generation, transport, and storage. However, despite thousands of studies which have incorporated SEM methods, the inability of SEM to differentiate sedimentary organic matter types has hampered the pace of scientific advancement. In this study, we show that SEM-cathodoluminescence (CL) properties can be used to identify and characterize sedimentary organic matter at low thermal maturity conditions. Eleven varied mudstone samples with a broad array of sedimentary organic matter types, ranging from the Paleoproterozoic to Eocene in age, were investigated. Sedimentary organic matter fluorescence intensity and CL intensity showed an almost one-to-one correspondence, with certain exceptions in three samples potentially related to radiolytic alteration. Therefore, because CL emission can be used as a proxy for fluorescence emission from sedimentary organic matter, CL emission during SEM visualization can be used to differentiate fluorescent from non-fluorescent sedimentary organic matter. This result will allow CL to be used as a visual means to quickly differentiate sedimentary organic matter types without employing correlative optical microscopy and could be widely and rapidly adapted for SEM-based studies in the geosciences.

Glycyrrhizae radix et rhizoma processing ameliorates adverse reactions of polygalae radix in zebra fish and rabbit models

Ethnopharmacological relevancePolygala tenuifilia Willd (Polygalaceae), a traditional Chinese medicine, has been used for a long time to treat various illnesses with serious adverse reactions. Glycyrrhizae radix et rhizoma processing is generally used to reduce the adverse reactions. Aim of the studyThe aim of this study was to validate the irritation caused by raw Polygalaceae (RPA), to investigate whether processed Polygalaceae (PGA) was less irritating, and to screen and validate irritant properties of virgaureagenin G (polygala acid, PA), 3,6′-disinapoylsucrose (DSS), Tenuifolia (TEN) and polygalaxanthone III (POL), which had pharmacologically active in Polygalaceae. Zebrafish model, Draize test and High-Performance Liquid Chromatography (HPLC) were utilized to achieve the aim. Materials and methodsScanning Electron Microscopy (SEM) and optical microscope were used to determine the presence of calcium oxalate needle crystal in RPA and PGA. Zebrafish egg spinning changes and zebrafish embryo behavior were used for irritation validation, irritation comparison and irritant screening. For additional evidence, the Draize test, HE staining of rabbit eyes and ELISA kit were used. Finally, changes in the composition of RPA and PGA were investigated using HPLC. ResultsSEM and optical microscopy revealed no calcium oxalate needle crystals in Polygalaceae. RPA, PGA, PA and DSS were able to accelerate the spinning of zebrafish eggs and the movement of embryos, while TEN and POL were not. RPA, PGA, DSS and PA may cause rabbit eyes to become hyperemic and swollen, resulting in damage to the iris, cornea and conjunctiva and increased levels of interleukin-6 (IL-6) and interleukin-10 (IL-10). Comparatively, the effects caused by PGA were less severe than those caused by RPA. In addition, compared to RPA, PGA had lower levels of DSS and PA. ConclusionsRPA, PGA, DSS, and PA were irritating. However, processing and curing could reduce the irritation by reducing the levels of DSS and PA. DSS and PA could be two potential irritants of Polygalaceae.

Li3V2(PO4)3 Cathode Material: Synthesis Method, High Lithium Diffusion Coefficient and Magnetic Inhomogeneity.

Li3V2(PO4)3 cathodes for Li-ion batteries (LIBs) were synthesized using a hydrothermal method with the subsequent annealing in an argon atmosphere to achieve optimal properties. The X-ray diffraction analysis confirmed the material's single-phase nature, while the scanning electron microscopy revealed a granular structure, indicating a uniform particle size distribution, beneficial for electrochemical performance. Magnetometry and electron spin resonance studies were conducted to investigate the magnetic properties, confirming the presence of the relatively low concentration and highly uniform distribution of tetravalent vanadium ions (V4+), which indicated low lithium deficiency values in the original structure and a high degree of magnetic homogeneity in the sample, an essential factor for consistent electrochemical behavior. For this pure phase Li3V2(PO4)3 sample, devoid of any impurities such as carbon or salts, extensive electrochemical property testing was performed. These tests resulted in the experimental discovery of a remarkably high lithium diffusion coefficient D = 1.07 × 10-10 cm2/s, indicating excellent ionic conductivity, and demonstrated impressive stability of the material with sustained performance over 1000 charge-discharge cycles. Additionally, relithiated Li3V2(PO4)3 (after multiple electrochemical cycling) samples were investigated using scanning electron microscopy, magnetometry and electron spin resonance methods to determine the extent of degradation. The combination of high lithium diffusion coefficients, a low degradation rate and remarkable cycling stability positions this Li3V2(PO4)3 material as a promising candidate for advanced energy storage applications.

High‐temperature resistant copolymer oil well cement retarder: Synthesis, assessment of performance, and mechanism of retardation

AbstractThis work used aqueous solution free radical polymerization to create polymers of 2‐acrylamide‐2‐methylpropane sulfonic acid, itaconic acid, and allyl polyoxyethylene ether as a high‐temperature resistant retarder (APMS/IA/APEG, from now on referred to as AIA). Gel permeation chromatography, fourier transform infrared (FTIR), proton nuclear magnetic resonance (1HNMR), and thermo‐gravimetric analysis (TG) were used to characterize their molecular structure and characteristics. Tests were conducted on the thickening time, rheological characteristics, and compressive strength of AIA in cement slurries. The cement slurry thickened for 276 min at 180°C during the test, and the cement stone's 24‐h compressive strength was consistently more than 20 MPa. The hydration products were analyzed using x‐ray diffractometer and scanning electron microscopy methods, which were then coupled with molecular dynamics simulations to elucidate the AIA retarding mechanism. When AIA is added to a cement slurry, it forms a chelate structure with Ca2+ and a strong adsorption layer on the surfaces of the cement particles. This stops the cement from hydrating. The AIA side chain, APEG, can wrap the active group in AIA at low temperatures. AIA exposes more adsorption groups because of the APEG chains stretching at higher temperatures. AIA can, therefore, be used for deep well operations at high temperatures.