Energy Dispersive X-ray Research Articles

Synthesis of ZnTe powders from green solvents by a solvothermal method. Study of the sensing properties in a CO atmosphere

In this work, the characterization and testing of sensing properties of ZnTe powders for detecting carbon monoxide were investigated. The ZnTe synthesis was reached by a solvothermal process, using three different green solvents, methanol, ethanol, and isopropanol. The structural, morphological, and compositional properties of ZnTe powders were analyzed by X-ray diffraction, XRD, scanning electron microscopy, SEM, and atomic force microscopy, AFM, and X-ray energy dispersion (EDS), respectively. XRD confirmed the zincblende-type cubic phase of ZnTe, with crystallite sizes of the order of 69 nm. SEM images of all synthesized samples showed a surface covered with particles of different sizes and irregular morphologies. Finally, the sensing response of ZnTe samples to CO was measured for concentrations varying from 1 to 500 ppm at different operating temperatures, 100, 200, and 300 °C. The highest sensitivity, 18.4, was obtained for ZnTe samples synthesized from isopropanol as solvent, so ZnTe powders showed a good response for CO detection, resulting these materials promising to be applied as gas sensors.

Green Synthesis of silver nanoparticles from clematis gouriana leaf extract: Physicochemical characterization and antibacterial activity determination for treatment of blood stream infections

BackgroundThe global incidence of bloodstream infections (BSIs) is rising, necessitating the development of effective therapeutic strategies to achieve complete eradication. This study focuses on the synthesis of silver nanoparticles (AgNPs) functionalized with Clematis gouriana extract (CG) (CG-AgNPs) as a potential alternative to conventional treatments for combating BSIs caused by bacterial pathogens. MethodsAgNPs were synthesized by reducing silver nitrate (AgNO₃) using CG extract. The formation of CG-AgNPs was confirmed through UV-Vis spectroscopy, while their characterization included the determination of mean particle size and zeta potential. Elemental composition was analyzed using energy-dispersive X-ray (EDX) spectroscopy. The in vitro antibacterial efficacy of CG-AgNPs was assessed through multiple assays, including a time-kill assay, a film bioadhesion assay, and measurement of reactive oxygen species (ROS) generation. ResultsSPR (surface plasmon resonance) has been employed to validate the development of AgNPs by observing a colour shift to dark brown. The mean particle size and zeta potential of the CG-AgNPs were found to be 38 ± 2nm (PDI 0.104 ± 0.03) and -31.2 ± 1.4mV, respectively. Additionally, E-XRD results show that the prepared AgNPs comply with the silver presence. The minimum inhibitory concentrations (MIC) and minimum bactericidal concentrations (MBC) of the CG-AgNPs against Staphylococcus aureus (S. aureus) were observed to be 6.25 ± 0.8µg/mL and 13.5 ± 2.4µg/mL, respectively.Similarly, the MIC and MBC of CG-AgNPs against Escherichia coli (E. coli) were found to be 13.5 ± 1.5μg/mL and 26 ± 2.8μg/mL, respectively. CG-AgNPs also prevented biofilm formation and bacterial adhesion in a dose-dependent manner; 100% inhibition was achieved in 48h at MBC. In addition, CG-AgNPs remarkably escalated the ROS level within cells, indicating their mechanism of antimicarobial activity. ConclusionsThe findings of this study demonstrate that CG-AgNPs synthesized via green synthesis exhibit significant antibacterial activity, highlighting their potential as an effective alternative for the treatment of BSIs. However, further in vivo studies are required to optimize a suitable dosage form and validate their therapeutic efficacy against bacterial infections in clinical settings.

Eco-toxicological impact of biologically synthesized FeONPs on rice plants and PGP bacteria

Nanoformulations of plant micronutrients can improve nutrient use efficiency and availability in plants compared to conventional fertilizers and, therefore, may prove helpful in addressing the widespread challenge of nutrient deficiency in agricultural soils. In this study, iron-oxide nanoparticles (FeONPs) were bio-synthesized using Aspergillus terreus cell-free extract and tested for bio-efficacy in rice (Oryza sativa L., ssp. japonica, T309) in situ. Physicochemical characteristics of biosynthesized FeONPs (B-FeONPs) were analyzed through UV-visible spectroscopy (UV-Vis), dynamic light scattering (DLS), X-ray diffraction (XRD), Fourier-transform infrared (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and energy-dispersive X-ray (EDX). Bio-efficacy was tested at both environmentally relevant concentrations (0-50 mg.kg−1) as well as supra-environmental concentrations (100 mg.kg−1). Germination, wet and dry biomass, root length, shoot length, chlorophyll and carotenoid content, and iron fortification in rice plants were evaluated under greenhouse conditions. Potential eco-toxic effects of B-FeONPs were investigated in multiple strains of plant growth-promoting (PGP) bacteria. A significant increment in plant growth parameters (p < 0.05), including wet biomass, dry biomass, root length, and chlorophyll and carotenoid content was observed in B-FeONPs treated rice plants as compared to those treated with bulk Fe-fertilizer FeSO4. B-FeONPs caused no oxidative stress and increased the % Fe content in the plants. Uptake and accumulation of the B-FeONPs were also confirmed in the roots and leaves of plants using TEM. The B-FeONPs did not demonstrate bactericidal activity against any of the tested strains of PGP bacteria at both environmentally relevant and supra-environmental concentrations. In conclusion, the data demonstrate that B-FeONPs exhibit significant potential in enhancing nutrient use efficiency and promoting growth in rice plants. These findings underscore the potential of B-FeONPs as sustainable alternatives to conventional Fe fertilizers, offering sustainable solutions for addressing nutrient deficiencies in agricultural soils.

Influences of Fluorine on Corrosion Behavior of FeCrAl Alloy in Lithiated/borated Water at 360 °C/18.5 MPa

Abstract As an accident-tolerant fuel cladding material, Iron-Chromium-Aluminium (FeCrAl) alloy shows a big potential in replacing zirconium alloy as the cladding tube for pressurized water reactors. The presence of fluorine impurity in the primary coolant of pressurized water reactors will accelerate the corrosion of fuel cladding tubes. However, studies on the influences of fluorine impurity on the service performance of FeCrAl alloy are relatively limited. In this work, corrosion behavior of FeCrAl alloy in fluorine-containing lithiated/borated water at 360 °C and 18.5 MPa was characterized by Scanning Electron Microscope (SEM), Energy Dispersive Spectrometer (EDS), X-ray diffractometer (XRD), and Raman spectroscopy. The results indicate that FeCrAl alloy exhibited relatively good resistance to fluorine attack. Fluorine ions changed the diffusion behavior of alloying element Cr, so facilitating the formation and dissolution of FeCr2O4. Deposition of Ni and B was observed on the alloy surface. The maximum content of B reached 24.20 at.% after fluorine-containing lithiated/borated water exposure while that was 12.50 at.% in the absence of fluorine ions. Despite this, no specific compounds of B were detected in the corrosion products, but Ni existed in the form of NiFe2O4.

Performance of high-energy storage activated carbon derived from olive pomace biomass as an anode material for sustainable lithium-ion batteries

In this work, we investigate how activated carbon (AC) derived from olive pomace biomass can be used as an anode material in lithium-ion batteries. The biomass-derived activated carbon has the potential to be highly efficient, deliver high performance, sustainable, and cost-effective in LIBs-related production. The activated carbon is prepared by using H3PO4 as a chemical activation agent, and then calcining the obtained product at 500°C for different controlled atmospheres under (i) air (AC-Atm), (ii) vacuum (AC-Vac), and (iii) argon (AC-Arg). The different samples were systematically analyzed using scanning electron microscopy (SEM), High-resolution transmission electron microscopy (HRTEM), energy dispersive spectroscopy (EDS), X-ray fluorescence (XRF), X-ray diffraction (XRD), FT-IR and Raman spectroscopy, and thermogravimetric analysis (TGA) to assess their properties. The electrochemical properties of the carbonaceous materials were studied by galvanostatic cycling, cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS). The results showed high specific capacity and stable cycling performance, with capacities of 288, 184, and 56 mAh g-1 at the current density of 25 mA g-1 after 70 cycles for AC-Arg, AC-Vac, and AC-Atm respectively. Furthermore, the CE efficiency was nearly 100% from the first cycles. This study opens up interesting prospects and offers promising opportunities for more efficient recovery of unused olive pomace waste, by integrating it into energy storage applications, particularly sustainable lithium-ion batteries.

Optoelectronic properties of Mg and Cu co-doped ZnO nanostructure

In this work, both pure and Mg-Cu co-doped zinc oxide thin films are prepared by sol-gel spin coating technique. Microscopic glass substrates are used for the synthesis of thin films. The thin films are examined by X-ray spectroscopy (XRD), photoluminescence spectroscopy (PL), scanning electron microscopy (SEM), ultraviolet-visible spectroscopy (UV-Vis), and energy dispersive X-ray analysis (EDX). The XRD reveals the hexagonal wurtzite phase of the films. The observed grain size is 23.34 nm to 15.94 nm for pure and Mg-Cu co-doped ZnO respectively. The SEM image shows an increase in grain size and a smoothing of the surface with Mg-Cu co-doping. The presence of Mg and Cu in the ZnO nanofilm is confirmed by EDX analysis. UV analysis shows an increase in percent transmittance with doping. The Tauc relation is used to estimate the band gap of the samples, and a significant shift in the band gap is observed. The photoluminescence diagram shows greater emission and surface defects with doping. The visible spectrum is completely covered by the low- level emission.

Improving concrete structures with engineered cementitious composites and kevlar sheets: an affordable retrofitting solution for earthquake resistance

Abstract This paper outlines experimental and analytical studies focused on strengthened concrete specimens using Engineered Cementitious Composites and use of Kevlar sheets is highlighted as one of the most effective techniques for achieving the desired structural reinforcement and extending the lifespan of structures. The research examines the mechanical properties of retrofitted concrete and material characterizations of ECC such as Scanning Electron Microscopy and Energy dispersive x-ray analyses were also carried out to corroborate the durability properties of ECC and Kevlar-wrapped specimens, specifically assessing compressive, tensile, and flexural strength. In this study, fiber-reinforced cementitious materials featuring a 2% volume fraction of hybrid fibers comprising hooked-end steel and polyvinyl alcohol fibers were employed to strengthen the concrete structure. This additional layer enhances tensile strength and aids in crack management, necessitating proper curing to ensure strength gain over a specified duration. Kevlar fabric sheets are carefully applied to the ECC surface using resin to create a strong bond between the Kevlar and the underlying material, resulting in a durable retrofitted structure. Preliminary experimental data supported numerical modelling of the specimens using finite element analysis. The numerical results regarding the retrofitted strength of hardened concrete were compared with experimental outcomes. The findings showed that the maximum load of the strengthened samples increased by 6.5%. Additionally, the retrofitted strength prior to complete failure rose by 10.6%. In conclusion, the integration of hybrid fibers for reinforcement and Kevlar for retrofitting proves to be a cost-effective and straightforward approach.

Green approach of cobalt sulfide nanoparticles from novel red stigma of Crocus sativus and multifaceted biomedical advancement

The present study was based on green protocols for synthesizing cobalt sulfide nanoparticles using saffron stigma flower extract (Crocus sativus), as saffron is considered a potent traditional medicine. Furthermore, the novel cobalt sulfide (CoS) nanoparticles prepared by the green approach for the first time with saffron improved showed cytotoxicity and antibacterial activity, as well as significant antitumor activity of Hela, A549, and MCF 7 cells viz in vitro studies. The saffron-cobalt sulfide nanoparticles underwent characterization using various techniques which include the X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Advances in scanning electron microscopy (SEM), and high-resolution transmission electron microscopy (HR-TEM), and the energy dispersive X-ray analysis spectroscopy. Both XRD, and FTIR confirmed the synthesis of pure cobalt sulfide nanoparticles. The resulting saffron-based cobalt sulfide nanoparticles exhibited a nanosphere structure, as confirmed by HRTEM, indicating the formation of nanosphere and microstructures. In vitro studies were conducted to assess the cytotoxicity and cell viability of Hela cells, A549, and MCF-7 cells. And, antibacterial studies were performed against various bacterial strains using different concentrations of cobalt sulfide nanoparticles derived from the red stigma of saffron (Crocus sativus) only the red stigma extract. The MTT assay analysis, cell viability, and morphological studies demonstrated the cytotoxic studies of the synthesized cobalt sulfide nanoparticles on cancer cells. The antibacterial test of the nanoparticles was also evaluated, revealing significant zones of inhibition (mm) against pathogens and cobalt sulfide nanoparticles using saffron extract, showcasing their potent cytotoxic, antibacterial, and antitumor activities with promising biomedical applications.

Surface enhanced Raman scattering-based sensing and ultrafast nonlinear optical properties of silver-hexagonal boron nitride nanocomposites achieved by femtosecond laser ablation

This study investigated the surface-enhanced Raman spectroscopy (SERS) properties and nonlinear optical (NLO) behavior of silver nanoparticles (Ag NPs) decorated hexagonal boron nitride (hBN) nanocomposites. Although Ag NPs are known for their excellent plasmonic properties, their susceptibility to oxidation in ambient conditions significantly reduces SERS activity. To overcome this, a femtosecond laser-assisted single-step novel approach is developed for synthesizing hybrid Ag-hBN nanocomposites via ablating Ag target in a solution of exfoliated hBN nanosheets, forming uniformly embedded Ag NPs on hBN nanosheets. The morphological characteristics and elemental compositions were validated by field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), and energy dispersive X-ray spectroscopy (EDS). TEM analysis revealed that Ag NPs averaged 15 nm in size, while hBN nanosheets had lateral dimensions of approximately 250 nm. The SERS activity of the prepared nanocomposites was investigated using dye and explosive molecules, achieving detection sensitivities of 1 μM and 100 μM, respectively, with high reproducibility. These detection sensitivities are significant as they demonstrate the potential of the Ag-hBN nanocomposites for sensitive and reliable detection of trace amounts of analytes. Notably, the Ag-hBN nanocomposites showed enhanced SERS activity compared to pure Ag NPs, with a 2.5-fold improvement for Nile blue, 3.6-fold for methylene blue, and 2.4-fold for RDX. The current study also demonstrates that hBN prevents Ag NPs’ oxidation and preserves the SERS functionality even at elevated temperatures. Furthermore, the NLO properties of the nanocomposites were investigated using the standard Z-scan technique, revealing two-photon and three-photon absorption coefficients of 3 × 10−4 cm/GW and 6.5 × 10−5 cm3/GW2, respectively. The findings highlight the potential of Ag-hBN nanocomposites to enhance SERS and NLO devices, enabling future applications in sensing and photonics.

Electrochemical Drawdown of U3+ and Ce3+ in Molten LiCl-KCl Using a Liquid Cadmium Cathode

Abstract The electrorefining of spent nuclear fuels is a key step to recover uranium and transuranium on separated cathodes. However, the electrolyte salts become contaminated with fission products after batches of electrorefining, and therefore the two unit processes for the drawdown of actinide and lanthanide are suggested before treatment of the contaminated salts. We investigated the electrochemical drawdown of U3+, Ce3+, and U3+ from Ce3+ in molten LiCl-KCl electrolyte using a liquid cadmium cathode (LCC) at 773 K. The drawdown mechanism of U3+ and Ce3+ was determined by cyclic voltammograms and calculating the equilibrium potential. After galvanostatic electrolysis, high recovery yields were obtained for the drawdown of U3+ and Ce3+, but the current efficiency of Ce3+ was at least twice as high as that of U3+ due to the cyclic electrolysis of U3+/U4+. Despite significant underpotential deposition of Ce3+ in the LCC, an exceptional separation factor for Ce relative to U reached 84.67 ± 17.13, which was attributed to the formed pure uranium products hindering the subsequent deposition of Ce3+. Moreover, pure uranium products and Ce-Cd intermetallic compounds were characterized by X-ray diffraction and scanning electron microscope coupled with energy dispersive X-ray spectroscopy.

Phase transformation and metallurgical characterization of heat-treated nickel–titanium rotary instruments using differential scanning calorimetry, X-ray diffraction, and energy dispersive spectrometry

Objective: The present study aimed to evaluate the phase transformation behavior and elemental analysis of thermomechanical-treated nickel–titanium (NiTi) rotary instruments, TruNatomy (Dentsply Sirona), HyFlex CM (coltene, Whaledent), and Neoendo Flex (Orikam healthcare India), using differential scanning calorimetry (DSC), X-ray diffraction (XRD), and energy dispersive X-ray spectrometry. Materials and Methods: A total of 18 NiTi rotary instruments, TruNatomy, Hyflex CM, Neoendo Flex, taper. 04, size 25 (except TruNatomy, size 26) were selected and were divided into three groups (n = 6). Three NiTi files from each group were investigated for the DSC test (n = 3). The two segments of each sample were cut carefully by slow-speed water-cooling carborundum disc at 3 mm from the tip and then 4 mm from the previous section. The mass of the samples was measured on the electronic balance and samples that weighed 10–15 mg were loaded into a 40 µL aluminum crucible. The samples are then subjected first to a heating cycle from 0°C to 100°C and subsequently a cooling cycle from 100°C to 0°C in the differential scanning calorimeter (Mettler-Toledo, NIT Srinagar) at a rate of 10°C min−1. XRD (Make. Rigaku Japan, smart lab 3kW, NIT Srinagar.) was performed to verify the DSC results. The remaining two samples from each group (n = 2) were subjected to XRD analysis. The sample preparation for XRD analyses was done precisely with slow speed water cooled carborundum disc and samples were sectioned into three segments. Each segment was 5 mm long and grounded to obtain a uniform smooth plane. The data obtained from DSC and XRD were subjected to origin 8.5 software and graphs were obtained that depict the transformation temperature and phase composition, respectively. Alloy distribution and trace elements of the NiTi rotary instruments were done using energy dispersive spectrometry microanalysis. Results: The DSC results showed that the TruNatomy, Hyflex CM, and Neo Endo instruments had an Austenite finish (Af) temperature exceeding 37°C. The XRD graphs show the different intensity peaks that correspond to the various phases of NiTi rotary instruments. The TruNatomy is predominantly Austenite, Hyflex CM exists mainly in R-phase with a variable amount of austenite and martensite, while Neoendo flex endo mostly contains austenite phase. The elemental analysis revealed that all three file systems show Nickel and Titanium within their bulk structure in an equiatomic ratio. Conclusion: This study concluded that TruNatomy is predominantly martensite with a variable amount of austenite phase. There are differences in thermal transition temperature between the files.

Role of Interfacial Hydrogen in Ethylene Hydrogenation on Graphite-Supported Ag, Au, and Cu Catalysts.

A combined surface science/microreactor approach was applied to examine interface effects in ethylene hydrogenation on carbon-supported Ag, Au, and Cu nanoparticle catalysts. Turnover frequencies (TOFs) were substantially higher for supported catalysts than for (unsupported) polycrystalline metal foils, especially for Ag. Spark ablation of the corresponding metals on highly oriented pyrolytic graphite (HOPG) and carbon-coated grids yielded nanoparticles of around 3 nm size that were well-suited for characterization by X-ray photoelectron spectroscopy (XPS), high-resolution (scanning) transmission electron microscopy (HRTEM/STEM), and energy dispersive X-ray spectroscopy (EDX). Polycrystalline metal foils characterized by scanning electron microscopy (SEM), EDX, electron backscatter diffraction (EBSD), XPS, and low-energy ion scattering (LEIS) served as unsupported references. Employing a UHV-compatible flow microreactor and gas chromatography (GC) allowed us to determine the catalytic performance of the model catalysts in ethylene hydrogenation up to 200 °C under atmospheric pressure. Compared to the pure metal foils, the HOPG-supported metal nanoparticles exhibited not only strongly increased activity but also higher stability (slower deactivation) and differing reaction orders. For the most active Ag catalysts, DFT calculations were carried out to determine the adsorption energies of the reacting species on single-crystal surfaces as well as on carbon-supported and unsupported Ag nanoparticles. Adsorption of molecular hydrogen was very weak on all unsupported Ag surfaces, resulting in hydrocarbon-"poisoned" surfaces. However, when a carbon support was present, the adsorption strength of H2 on Ag nanoparticles increased on average by -0.5 eV, driven by changes in Ag-Ag distances near the metal-carbon three-phase boundary (whereas subsurface carbon lowers hydrogen bonding). On Cu particles, the interface effect was calculated to be somewhat weaker than for Ag particles. H2/D2 scrambling experiments on Ag catalysts then corroborated a facilitated hydrogen activation for carbon-supported metals. Thus, the carbon support effect is attributed to an improved hydrogen availability at the metal-carbon interface, controlling performance.

Investigation and estimation of structural and dielectric properties of chromium-doped cobalt ferrites nano particles

Abstract Nano ferrite materials are of critical importance in meeting the global demand for microwave and electronic devices, as spinel ferrites possess remarkable morphological, structural, and dielectric characteristics. This study investigates chromium-doped ferrite nanoparticles with the chemical composition CoCrxFe2-xO4 (x = 0.00, 0.30, 0.60, and 0.90), synthesize using the sol–gel technique and subjected to annealing at 900 °C. Energy Dispersive x-ray Analysis EDAX patterns confirmed compositional stoichiometry. X- Ray Diffraction analysis reveals that all samples exhibit a cubic crystal structure. Replacing some of the ions with chromium (Cr3+) led to a decrease in the x-ray density form (5.329–5.324). The average crystallite size in the fabricated samples ranged from 46.07 to 31.84 nm, and the lattice parameters decrease from 8.382 to 8.364 Å as the chromium content increase. Infrared spectra show that lower frequency band (ν2) at around 479.69-392 .60 cm–1 and a higher frequency band (ν1) within a range from 611.05–57661 cm–1 a clear indication of spinel structure characteristics. The examination using FE-SEM indicates that the produced materials exhibit porosity and amorphous characteristics. The significant tangent loss observe at lower frequencies suggests that these materials may have potential applications in medium-frequency devices. Consequently, spinel nanoferrites can offer advantages for advanced electronic and microwave technologies.

Sustained release of heparin from PLLA micropartricles for tissue engineering applications

Heparin holds promise for cardiac tissue engineering, but challenges such as hematoma or bleeding and accumulation in tissue caused by excessive release, and short half-life persist. The present study aimed to introduce a reliable mechanism for the prolonged heparin release from a biocompatible polymer carrier. The designed system must ensure that heparin retains its bioactivity over time while preventing premature release. Heparin was encapsulated within poly (L-lactic acid) microparticles using the double emulsion method, with polyvinyl alcohol employed as the stabilizer. The encapsulation efficiency of heparin in the microparticles was calculated as 25.56 %. The functionality of the design was evaluated using Attenuated Total Reflection Fourier Transform Infrared Spectroscopy, Scanning Electron Microscopy, and Energy Dispersive X-ray Spectroscopy. Drug release and microparticle degradation studies were conducted alongside cell viability tests. The particle sizes ranged from 5 to 10 ± 2.53 μm, with evidence suggesting that heparin promotes the smaller particle formation. The system demonstrated a consistent drug release profile over six weeks with a release rate of 54 % by week two and 97.65 % by week six. The degradation of heparin-loaded microparticles reached less than 50 % by week six, and the loading of heparin did not significantly affect the degradation behavior of the PLLA microparticles in PBS. Furthermore, heparin concentrations between 200 and 400 μg/ml enhanced the viability of Placenta-derived Mesenchymal Stem Cells and H9c2. These findings suggest that the system could be considered as an effective vehicle for sustained heparin delivery across a spectrum of biological applications, particularly in cardiac tissue engineering.

Correlation between structural modifications and physical parameters of Sb doped InSe alloys for optoelectronic applications

Bulk samples of In0.1Se0.9-xSbx (0 ≤ x ≤ 0.24) were synthesized using the conventional melt-quenching technique. The impact of Sb doping on the structural and physical properties of InSe alloys was systematically explored. The substitution of Sb at the expense of Se introduces defects and dislocations in the lattice, which significantly influence the properties of the InSeSb system. With increasing Sb content, physical parameters such as the average coordination number, cross-linking density, mean bond energy, and cohesive energy were observed to increase. Theoretically calculated band gap values lie between 1.7 and 1.3 eV. X-ray diffraction (XRD) analysis confirmed the polycrystalline nature of the alloys, revealing the coexistence of rhombohedral α-In2Se3 and orthorhombic Sb2Se3 phases. Energy dispersive X-ray spectroscopy (EDX) confirmed the elemental composition, showing the presence of In, Se, and Sb in the bulk samples. Raman and FTIR spectroscopy further validated the presence of distinct structural units and molecular bonds as a function of Sb content, confirming the coexistence of α-In2Se3 and Sb2Se3 phases alongside In–Se, Se–Se, and Sb–Se bonds. A strong correlation was established between the experimental findings and theoretically calculated parameters, including the average coordination number, mean bond energy, glass transition temperature, cohesive energy, and optical band gap. This study provides a comprehensive insight into the compositional dependence of structural and physical properties in InSeSb chalcogenide alloys, enhancing our understanding of their potential applications.

Investigation of the microstructure, electrical and mechanical properties of Al-CNTs-B4C composite prepared by double-step stir casting for power transmission conductor

Abstract Monolithic aluminium alloy is a modern engineering material that is in high demand owing to its excellent performance and versatility. It has a high electrical conductivity, low density, high strength- to- weight ratio, and high resistance to corrosion. However, it lacks adequate resistance to creep, fatigue, stable microstructure, and strength at elevated temperatures. To overcome these deficiencies, aluminium matrix composites are developed. This work focuses on an experimental investigation of the microstructure, mechanical strength, and electrical conductivity of Al-CNTs-B4C composite consolidated by a double-step stir casting technique. An x-ray diffractometer, transmission electron microscopy, and a field-emission scanning electron microscope fitted with energy dispersive x-ray spectroscopy were used to characterize the start-up powders and the cast samples. A Brinell tester was used to measure the microhardness of the cast samples. A four-point probe meter was used to determine the electrical conductivity. The microstructural results revealed formation of Al4C3 and Al3BC intermetallics, B4C phase and amorphous carbon precipitate. Marginally improved electrical conductivity of 33.33 × 107 S m−1 (65.1% IACS) was obtained with Al-5CNTs-15B4C, together with high microhardness of 725.72 MPa. The microhardness improved by 94.7% over monolithic pure Al. The double-step stir casting enhanced the homogenous dispersion of the reinforcements. The improvements in the mechanical properties and electrical conductivity were attributed to the synergy between B4C and CNTs which induced Orowan looping, load transfer effect, plastic deformation and dislocation pinning in the composite. It is recommended that this composite will perform creditably in power transmission.

Impact of Dual-coated Silver Nanoparticle and Antibiotic Sutures on Wound Healing in Inflammatory Mouse Models

ABSTRACT Background: The use of silver nanoparticles (AgNPs) in biomedicine has emerged in a big way owing to its antibacterial and anti-inflammatory properties. We hypothesize that combining the AgNPs with antibiotics for coating sutures will enhance the antibacterial property of sutures with the added advantage of the immunomodulatory effect of AgNPs on tissue healing. Materials and Methods: Polyglactin sutures were coated with AgNPs using the dip-coating method. The uniform coating and morphology of AgNPs on the suture surface were confirmed using scanning electron microscopy (SEM). Each type of suture – polyglactin plain, antibiotic coated (Triclosan), AgNP coated, and dually coated (antibiotic and AgNP) – was assessed for their antibacterial properties against Gram-positive bacteria, Gram-negative bacteria, and anaerobes. These sutures were utilized in an abdominal and systemic inflammatory mice model for ileal anastomosis. The intestinal tissue was evaluated for acute and chronic inflammation and collagen deposition to assess the healing and inflammatory response. Results: The SEM and energy dispersive X-ray analysis showed successful coating of AgNPs on plain and antibiotic-coated sutures. In comparison with the other groups, the dually coated suture had the best in vitro antibacterial efficacy. The AgNP-coated sutures were able to decrease both acute and chronic inflammatory cell infiltration, but the collagen synthesis and deposition were enhanced. Conclusion: AgNPs can be coated on Polyglactin suture either alone or in combination with antibiotics with preserved antibacterial effects. The dual coating of sutures gives a synergistic antibacterial effect. The AgNP diminishes immune response in the presence of preserved extracellular matrix generation.

Biochar as an Enzyme Immobilization Support and Its Application for Dye Degradation

Wastewaters generated by the textile industry often contain significant amounts of harmful (carcinogenic and mutagenic) cationic dyes, whose efficient removal is of crucial importance. This study investigates the laccase immobilization on biochar obtained from sour cherry stones (SCS-B), as a cost effective adsorbent, and evaluates its application for brilliant green (BG) degradation. The successful immobilization of laccase on biochar was achieved via adsorption and confirmed using scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX) and Fourier transform infrared spectroscopy (FTIR). An immobilization efficiency of 66% was achieved using 0.274 U/mL of laccase at pH 5 and a temperature of 40 °C. The adsorption kinetics of laccase followed a pseudo-second-order model, indicating that chemical adsorption plays a significant role in the immobilization process. The BG degradation by immobilized system was further optimized by evaluating effects of pH, temperature, dye concentration, and contact time. More than 92% of BG (50 mg/L) was removed within 4 h at pH 5 and temperature of 30 °C. These findings suggest that SCS-B can effectively be used as an enzyme carrier and be further utilized for the removal of emerging pollutants, positioning it as a sustainable solution for wastewater treatment.

Microscopic characteristics and corrosion rate modeling in galvanized high-strength steel wires

The electrochemical reaction mechanism of galvanized high-strength steel wires (GHSSWs) has not been fully elucidated. Scholars have observed a significant discrepancy between the theoretical mass loss rate calculated using the Faraday equation for electrochemical corrosion and the experimental values. To address this issue, this study conducted electrochemical corrosion tests on 195 sets of GHSSWs. Scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS) and non-contact 3D scanning systems were used to characterize the surface morphology and elemental composition of specimens before and after rust removal, revealing the reaction mechanism during electrochemical corrosion in GHSSWs. The correlation between corrosion length, current intensity, and electrolysis time with the corrosion rate was investigated, and a correction function for mass loss in GHSSWs under constant current electrochemical corrosion was established. The results indicate that during the initial stage of electrochemical corrosion in GHSSWs, internal stress between the corrosion products and the GHSSWs substrate leads to the formation of apparent cracks in the corroded wire, increasing the contact area between the specimen and the electrolyte and accelerating the corrosion process. In later stages, the formation of needle-like α-FeOOH corrosion products provides protective effects, leading to a decrease in the corrosion rate.

Investigation of the chemiluminescence behavior of Ti3C2 MXene quantum dots as a sensing platform for uric acid

The current study explores the application of Ti3C2 MXene quantum dots (MQDs) as a chemiluminescent (CL) probe to determine uric acid (UA) in biological samples. The MQDs sensor was synthesized using ultrasonic-assisted hydrothermal method and characterized through Fourier transform infrared spectroscopy, Raman spectroscopy, scanning electron microscopy, energy dispersive X-ray analysis, high-resolution transmission electron microscopy, and X-ray diffraction. The presence of MQDs significantly enhances the ultra-weak Fe(II)–S2O82− CL system. Subsequently, quenching of the probe’s CL signal was observed in the presence of UA. Thus, the designed CL sensor offers an excellent analytical capability for determining UA in the 0.15–2.5 µM range, with a limit of detection of 0.093 µM. The method was effectively used to analyze UA in human serum and urine, yielding recovery rates between 94.4 % and 108.3 % with relative standard deviations (RSD) ranging from 1.9 % to 5.9 %.