Conductivity Measurements Research Articles

Novel nano-Y2O3/myristic acid nanocomposite PCM for cooling performances of electronic device with various fin designs

Effective thermal management is critical for enhancing the longevity and operational efficiency of electronic devices. This research introduces a novel cooling approach by incorporating Yttrium Oxide (Y2O3) nanoparticles into Phase Change Materials (PCMs) to improve thermal management in electronic devices. This study focuses on developing nanocomposite PCMs with Y2O3 nanoparticles embedded in a myristic acid (MA) matrix through melting and physical mixing. Nanoparticles were added to MA at various mass fractions: 0.5 %, 1 %, 1.5 %, and 2 %. Structural and morphological analyses were conducted using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), and field emission scanning electron microscopy combined with energy dispersive X-ray spectroscopy (FE-SEM-EDX). Thermophysical properties were characterized using differential scanning calorimetry (DSC) and thermal conductivity measurements with the KD2-Pro device. The inclusion of Y2O3 nanoparticles significantly enhanced the thermal conductivity of the PCM, reaching up to 0.229 W/m·K in the solid phase and 0.177 W/m·K in the liquid phase, representing improvements of 43.125 % and 18 %, respectively, over the base PCM. The highest average specific heat capacity (Cp) values in the solid and liquid phases were 1.98 J/g·°C and 2.69 J/g·°C, respectively, for the 2 % nanoparticle-additive sample. DSC analysis indicated slight shifts in phase transition temperatures and a noticeable reduction in latent heat values, from 215 J/g to 202 J/g for solidification and from 209 J/g to 201 J/g for melting. Computational analysis using ANSYS-FLUENT software validated the enhanced thermal dissipation properties of the nanocomposite PCM. Additionally, an examination of fin configurations within the PCM containers revealed that rectangular fins provided superior cooling efficacy compared to trapezoidal ones. This study demonstrates that the development of nano- Y2O3 enhanced MA nanocomposite PCMs presents a promising avenue for applications in electronic device thermal management and thermal energy storage.

A New Numerically Improved Transient Technique for Measuring Thermal Properties of Anisotropic Materials

A new transient technique of the thermal conductivity and diffusivity measurement for anisotropic materials is presented and validated. It is based on measuring the through-plane properties using the extended dynamic plane source (EDPS) method and in-plane conductivity employing the transient plane source (TPS) and modified dynamic plane source (MDPS) methods. The key advantage of this technique is that only one pair of specimens is required for measurements. While the EDPS method is implemented on real measurements, the TPS and MDPS are applied to the finite elements method (FEM) simulation of the experiment. The accuracy of the results is enhanced by the application of the FEM and is better than 1% for materials with through-plane conductivity of less than 2 W m−1 K−1 and a specimen thickness of 9 mm.

Synthesis and Characterization of Coconut-Derived Graphene Nano Sheet (GNS) and Its Properties in Nickel/GNS and Zinc/GNS Hybrid Electrodes

This study introduces a sustainable method of producing a graphene nano sheet (GNS) from coconut shells and investigates its application in GNS, Ni/GNS, and Zn/GNS electrodes for advanced energy storage devices. The GNS was synthesized in a scalable manner using a pyrolysis and impregnation technique, with its successful synthesis verified by X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDX), Raman spectroscopy, and electrical conductivity measurement characterizations. The study highlights the enhanced performance of Zn/GNS electrodes, which outperform both pure GNS and Ni/GNS variants. This superior performance is attributed to the smaller particle size of Zn (mean = 2.356 µm) compared to Ni (mean = 3.09 µm) and Zn’s more favourable electron configuration for electron transfer. These findings demonstrate the potential of bio-derived GNS composites as efficient, high-performance electrodes, paving the way for more sustainable and cost-effective energy storage solutions.

Effect of Ca doping at A or B sites on electrochemical performance of La1.9In0.1Ce2O7 proton conductors

Fluorite proton conductors La1.8In0.1Ca0.1Ce2O7-δ and La1.9In0.1Ce1.9Ca0.1O7-δ (LICaC and LICCa) were synthesized by solid state reaction. The effect of Ca doping at A site or B site on La1.9In0.1Ce2O7 was studied by X-ray diffraction (XRD), Inductively Coupled Plasma Mass Spectrometry (ICP), scanning electron microscopy (SEM) and electrical conductivity measurement. XRD shows that the LICaC and LICCa were successfully synthesized, and Ca was doped to the expected sites. The measured mass ratios of each element by ICP were in good agreement with their theoretical values. In addition, SEM also found that the surface of the sample was dense without holes. The conductivities of LICaC and LICCa were studied at 400–800 ℃, and their highest conductivities were 7.28×10−4 and 5.56×10−3 S·cm−1, respectively. The conductivity of LICCa doped at the B site is better than that of LICaC doped at the A site. In the wet air at 800 ℃, the proton transference numbers of LICaC and LICCa are 0.5 and 0.52, respectively. LICaC and LICCa were used as electrolytes to prepare fuel cells and their performance was tested. The electrolyte thickness of LICAC and LICCA was about 0.9 mm. At 700 ℃, the maximum power density of LICaC and LICCa electrolyte-based single cells are 124.51 and 162.26 mW cm−2, respectively. The results show that LICCa has good proton conductivity and has potential as an electrolyte for high-performance fuel cells.

Electrochemical and computational evaluation of hydrazide derivative for mild steel corrosion inhibition and anticancer study

In the present study the authors’ main goal is to avoid the corrosive attack of the chloride ions of 3.5% NaCl solution in saline medium on the mild steel (MS), by addition of small amount of a new derivative of the hydrazide called ligand (HL), as a corrosion inhibitor. This study had been achieved by employing different electrochemical measurements such as, open circuit potential (OCP), electrochemical impedance spectroscopy (EIS) and potentio-dynamic polarization (PDP) methods. The results of the electrochemical test (OCP), showed that, the open circuit potential of the mild steel in saline solution, was guided to more positive direction in presence of the ligand (HL), at its ideal concentration (1 × 10−3 M), compared to the (OCP), of the mild steel in absence of (HL). The results of the electrochemical methods, EIS and PDP presented that, the ligand (HL), was acted as a good corrosion inhibitor for hindering the corrosion process of the mild steel in 3.5% sodium chloride, as it was recorded a good percentage of the inhibition efficiency (77.45%, 53.41%, by EIS and PDP techniques respectively), at its optimum concentration (1 × 10−3 M). Also, the corrosion rate of the mild steel in the saline medium without (HL), was listed about (0.0017 mm/year), while in existence of (HL), was decreased to a value about (0.00061 mm/year). As well, some of electrical properties of (HL), and its derivative [Pd(II), Cr(III), and Ru(III)], complexes were investigated such as; the activation energy (Ea(ac)), which recorded values in the range of 0.02–0.44 (eV) range and electrical conductivity which listed values at room temperature in the range of 10−5–10−8 S.cm−1. The results of the AC and DC electrical conductivity measurements for (HL), and its derivative [Pd(II), Cr(III) and Ru(III)] complexes indicate semiconducting nature which suggests that these compounds could be used in electronic devices. Also, the complexes exhibited higher conductivity values than (HL). Photophysical studies showed good florescence properties of HL that indicated that it can be used to determine most of the drugs with no fluorescence properties by quenching and calculating quantum yield. Moreover, the hydrazide ligand (HL), has shown selectivity as an active anticancer candidate drug for both breast and colon cancer in humans. Density function theory demonstrated that, the frontier molecular orbital HOMOs of the complexes have exhibited similar behavior and the charge density has localized in the metallic region of all the studied complexes. Also, the values of the energy gap of the ligand (HL), and its complexes Pd(II), Cr(III) and Ru(III), had been arranged in this order HL > Cr(III) > Ru(III) > Pd(II). All characterization using different spectroscopic techniques were reported to elucidate the proposed structures such as; thermal analysis, elemental analysis of C, H, and N atoms, spectral analysis using IR, UV, 1H NMR techniques, scanning electron microscopy and energy dispersive X-ray analyses.

Study on the electrical performance degradation mechanism of β -Ga2O3 p-n diode under heavy ion radiation

The impact of heavy ion irradiation on the β-Ga2O3 p-n diode and its physical mechanism have been studied in this Letter. After the irradiation fluence of 1 × 108 cm−2, it is observed that the electrical performance of the device is significantly degraded. The forward current density (JF) is reduced by 49.4%, the reverse current density (JR) is increased by more than two orders of magnitude, and the breakdown voltage (VBR) is decreased by 30%. Based on the results of the deep-level transient spectroscopy measurement, it is concluded that acceptor-like traps generated with an energy level of EC-0.75 eV in the β-Ga2O3 drift layer dominate the JF degradation of the device, which are most likely related to Ga vacancies. These acceptor-like traps result in the reduction of change carrier concentration, which in turn leads to a decrease in JF. In addition, according to the conductive atomic force microscope measurements and theoretical calculation, it is clearly observed that the latent tracks induced by heavy ion irradiation can act as leakage paths, leading to a significant degradation of JR and VBR.

Characterizing Flow Dynamics in a Two-dimensional Flow Cell: Developing Methodologies for Enhanced Subsurface Contaminant Remediation Research

This study used a two-dimensional (2-D) flow cell apparatus (25 cm × 25 cm × 1 cm) to characterize water flow and contaminant transport in porous media. The primary objective was to enhance the understanding of flow dynamics and contaminant behavior in controlled 2-D environments, which is crucial for optimizing the application of remediation technologies to treat contaminants in saturated and unsaturated soil conditions. The 2-D cell was designed with transparent walls to simulate subsurface conditions using medium grained sand, allowing for precise control and observation of fluid movement under saturated and quasi-saturated (trapped air) conditions. Visualization techniques and flow measurement tools were employed to capture detailed data on flow patterns, velocities, and dispersion characteristics. Analysis of breakthrough curves for salt tracer tests using electrical conductivity measurements, alongside varying flow rates, flow fractions, and port configurations, provided significant insights into fluid behavior and contaminant transport. The study also explored the effects of varying salt concentrations (and solution densities) on flow dynamics, contributing to a better understanding of the role of contaminant concentration in contaminant plume development and remediation processes. Visual analysis using dyed contaminant complemented the quantitative data, offering real-time observations of flow patterns and contaminant distribution. A custom-built apparatus was used to control the hydraulic head of multiple outlet ports to sample water from different depths. The experiments demonstrated that gravity plays a crucial role in solute (salt) breakthrough, with lower ports showing earlier breakthrough. Flow fields formed vertically, from bottom-to-top, and horizontally, from inlet-to-outlet, with lower portions advancing sooner. However, multi-port configurations, especially involving five ports, disrupted the sequential breakthrough order, possibly due to convection in the clear well that formed the outlet boundary of the flow cell. These findings will support research students in conducting similar experiments with flow and transport that varies with depth, with future insights for professionals in developing and optimizing remediation strategies related to subsurface contaminant flow. Special thanks are extended to Liam Price, Julia-Barnes James, and Brooke Belfall who were helpful during the research and the experimentation process.

Exploration of micellization and phase separation nature of surfactants in metformin hydrochloride + additives media: An experimental and DFT study

The study explores the aggregation and phase separation of a newly synthesized cationic surfactant − octadecyltriethylammonium bromide (OTEAB) and triton X-100 (TX-100) respectively with/without metformin hydrochloride (MMH) drug in absence/presence of NaCl. The conductivity measurements were performed to investigate the aggregation of cationic OTEAB at temperatures between 298.15 and 323.15 K with a 5 K gap. The micelle development of OTEAB in pure state and with MMH drug has been assessed by determining the critical micelle concentration (CMC). The reduction of CMC of OTEAB has been detected owing to the introduction of the MMH drug. The CMC was further decreased in attendance of NaCl. The CMC values also demonstrate the dependency on the change of temperature in all situations investigated. The decrease of CP values of triton X-100 and MMH mixture in aqueous NaCl was attained with the augmentation of the concentration of NaCl. The negative and positive values of free energy of micellization (ΔGm0) and clouding (ΔGc0) indicate the spontaneous and nonspontaneous nature of the respective processes. The enthalpy (ΔHm0) and entropy(ΔSm0) changes of the micellization were negative (exothermic) and positive, respectively. The enthalpy (ΔHc0) and entropy(ΔSc0) changes of the clouding were negative (exothermic) and positive, respectively, at lesser and higher concentrations of NaCl. The values of ΔHm0/ΔHc0 and ΔSm0/ΔSc0 designated that both hydrophobic and electrostatic interaction are present as important forces among the components under investigation. The thermodynamics of transfer and the enthalpy-entropy compensation parameters for the two processes were also computed and explained appropriately. Herein, we have also performed the computational analysis to find out the optimized structures, HOMO-LUMO orbitals, and the band gaps of OTEAB, MMH, and OTEAB+MMH mixture.

Selective attention and sensitivity to auditory disturbances in a virtually-real Classroom: Comparison of adults with and without AD(H)D.

Many people, and particularly individuals with Attention Deficit (Hyperactivity) Disorder (AD(H)D), find it difficult to maintain attention during classroom learning. However, traditional paradigms used to evaluate attention do not capture the complexity and dynamic nature of real-life classrooms. Using a novel Virtual Reality platform, coupled with measurement of neural activity, eye-gaze and skin conductance, here we studied the neurophysiological manifestations of attention and distractibility, under realistic learning conditions. Individuals with AD(H)D exhibited higher neural responses to irrelevant sounds and reduced speech tracking of the teacher, relative to controls. Additional neurophysiological measures, such the power of alpha-oscillations and frequency of gaze-shifts away from the teacher, contributed to explaining variance in self-reported AD(H)D symptoms across the sample. These ecologically-valid findings provide critical insight into the neurophysiological mechanisms underlying individual differences in the capacity for sustained attention and the proneness to distraction and mind-wandering, experienced in real-life situations.

Proton conductivity and dielectric studies on chitosan/polyvinyl alcohol blend electrolytes: Synergistic improvements with ionic liquid and graphene oxide

This study investigates the impact of ionic liquid, 1-methylimidazolium tetrafluoroborate (IL) and graphene oxide (GO) on the performance of chitosan/polyvinyl alcohol (CS/PVA)-based composite electrolytes. Fourier-transform infrared (FTIR) spectroscopy and scanning electron microscopy (SEM) confirm the successful incorporation of IL and GO, affecting the structural and morphological properties of the electrolytes. Thermogravimetric analysis (TGA) reveals enhanced thermal stability in GO-doped samples, with increased residual weight at high temperatures, while IL addition leads to higher initial weight loss due to its hygroscopic nature. Ionic conductivity measurements demonstrate that the CS/PVA/IL-GO(4.0) composite achieves the highest proton conductivity of 1.76 × 10−3 S/m at 300 K and 1 MHz, surpassing other samples and aligning with top values reported in literature. Dielectric studies show a significant increase in dielectric constant to 9.55 × 104 at 300 K and 20 Hz for CS/PVA/IL-GO(4.0), attributed to enhanced dipole alignment and polarization effects. The loss tangent analysis indicates the shortest relaxation time of 2.07 × 10−4 s for CS/PVA/IL-GO(4.0), correlating with its superior proton conductivity. These findings highlight the potential of CS/PVA/IL-GO electrolytes for advanced energy storage and conversion applications, suggesting further research into GO dispersion and long-term stability for optimized performance in practical devices.

An updated terrestrial heat flow data set for the Junggar basin, northwest China: implications for geothermal resources

SUMMARY Terrestrial heat flow plays a vital role in determining the present thermal regimes of sedimentary basins, offering a robust foundation for understanding hydrocarbon maturation processes and the geothermal resource potential. The Junggar basin is one of the largest and most petroliferous superimposed petroleum basins in China. However, research on heat flow is scarce. In this study, 94 new high-quality heat flow values are derived from through borehole temperature analysis and thermal conductivity measurements of rocks. The results indicate that (1) the geothermal gradient in the basin varies from 11.4 to 28.3 °C km−1, with a mean value of 20.9 ± 3.4 °C km−1, and the heat flow varies from 23.4 to 64.5 mW m−2, with a mean value of 45.1 ± 8.4 mW m−2. The overall low geothermal gradient and heat flow are attributed to the continuous cooling during the Meso-Cenozoic. (2) At basin scale, the high heat flow values are primarily concentrated in areas characterized by basement uplift, whereas the low heat flow values are mainly located in the depressions. This suggests that thermal refraction is the primary factor influencing the heat flow variations. (3) Although large-scale development and utilization of geothermal resources face challenges, certain local areas in the basin show promise for geothermal resource utilization.

Heterocyclic Schiff Base Complexes of Bivalent Transition Metals: Microwave-Assisted Green Synthesis, Structure Elucidation and Antimicrobial Studies

A heterocyclic Schiff base ligand [LH] namely {5‐[(E)‐[(1H‐pyrrol‐2‐yl)methylidene]amino]‐ 1,3,4‐thiadiazole‐2‐thiol}(NNN donor) and its divalent transition metals (Co2+, Ni2+, Cu2+ and Zn2+) mononuclear complexes were synthesised efficiently in relatively very short times (from one-two hours to 6-15 minutes) with higher yields [from 59% (conventional method) to 90% (green method)] by microwave-assisted greener process is presented here. The ligand and its complexes were characterised by elemental analysis, molar conductance, and magnetic susceptibility measurements and spectroscopic (IR, electronic, and NMR) analyses. All investigated complexes were found to be six coordinated ML2 [1:2 (metal: Ligand) ratio] type which possessed mononuclear octahedral geometry. The ligand and its metal complexes were screened for antimicrobial activity by the disc diffusion method, and the results indicate that the metal complexes are better antimicrobial agents compared to the Schiff base and the metal complexes have followed antimicrobial trends: Cu(II) complex > Co(II) complex > Ni(II) complex > Zn(II) complex > Schiff base

Reference Materials for Thermal Conductivity Measurements: European Situation

A reference material (RM), as defined by the International Vocabulary of Metrology (VIM 2012), must be homogeneous, stable, and suitable for use in measurements. Certified reference materials (CRMs) are RMs with documented property values, uncertainties, and traceability. ISO 17034:2018 outlines the requirements for RM producers, ensuring that CRMs meet standards for stability, uniformity, and reproducibility. In Europe, CE marking, from French “conformité Européenne”, which means European conformity, has been mandatory for thermal insulation products since 2002, ensuring their thermal performance is verified by accredited laboratories using RMs like IRMM440 and ERM FC440. Annually, European manufacturers produce over 200 million cubic meters of thermal insulation, necessitating thousands of thermal conductivity measurements daily to maintain CE marking compliance. Key characteristics of Reference Materials include long-term stability, thermal conductivity within specified ranges, and minimal dependence on density, thickness, and applied load. Sample thickness must conform to apparatus specifications, and homogeneity must be quantified. Reference Materials must also have appropriate dimensions, surface smoothness, and manufacturability. The Joint Research Centre (JRC) Geel has produced two Reference Materials, IRMM 440 and ERM FC 440, with specific characteristics to meet these requirements. Both are glass wool fibers with low thermal conductivity and specific density and thickness. The qualification of RMs involves inter-laboratory comparisons to ensure the accuracy and traceability of thermal conductivity measurements. The European market’s organization, including the use of Reference Materials and CE marking, has significantly improved measurement consistency and product quality. This system has led to lower uncertainties in thermal conductivity measurements compared to North America, highlighting the impact of standardized RMs on industry practices. Future needs include developing RMs with lower conductivity and increased thickness to accommodate market trends towards super insulation materials and bio-based components, enhancing energy performance calculations for buildings. This paper will present the process of defining a reference material and how it affects the uncertainty level of the calculation of building energy performance. This level depends on the characteristics of the materials used, their implementation, and external factors, such as the weather, as well as the reference material used for calibration of all European thermal conductivity measurement devices.

Flavonol derivatives containing piperazine and quinoxaline fragments: synthesis and antifungal activity.

A series of flavonol derivatives containing piperazine and quinoxaline had been designed and synthesized. The biological activity test results showed that some of the target compounds had good antifungal activity against various fungi. N5 had the best antifungal activity against Phomopsis sp (P.s.) and Phytophthora capsica (P.c.). The half maximal effective concentration (EC50) was 12.9 and 25.8μg/mL against P.s. and P.c., respectively, which were better than azoxystrobin (Az, 25.4 and 71.1μg/mL). In addition, the protective and curative activities of N5 against kiwifruit were 85.9 and 67.0% at 200μg/mL in vivo, which were better than that of Az (65.9 and 57.0%). The protective and curative activities against chili leaves were 80.6 and 66.5% at 200μg/mL, which were better than that of Az (77.6 and 60.0%). The scanning electron microscopy (SEM) experiment showed that the action of N5 caused the mycelium to bend and fold, changed its morphology and caused damaged to the mycelium. Through the measurement of relative conductivity, leakage of cytoplasmic contents and determination of malondialdehyde (MDA) content indicated that N5 could damage the integrity of pathogenic fungal cell membranes, change the permeability of cell membranes, and affect the normal growth of mycelium.

LC-MS based metabolomics identification of natural metabolites against Fusarium oxysporum.

Fusarium is a soil-borne pathogen that poses a serious threat to the quality and yield of hundreds of crops worldwide, particularly tobacco production. Using metabolomics technology, we investigated natural metabolites from disease-conducting soil (DCS) and disease-suppressing soil (DSS) of tobacco rhizosphere as fungicides to control tobacco Fusarium wilt (TFW), which is mainly caused by Fusarium oxysporum. Furthermore, the antifungal mechanisms of these natural metabolites were preliminarily elucidated through various assessments, including antifungal activity determination, chemotaxis effect tests, PI staining experiments, and measurements of extracellular conductivity and protein content. Metabolomics results showed that the DCS with three different disease grades (G1, G5 and G9 groups) had significantly higher levels of 15, 14 and 233 differential rhizosphere metabolites (DRMs) and significantly lower levels of 72, 152 and 170 DRMs compared to the DSS (G0 group). According to KEGG pathway analysis, these DRMs were found to be enriched in the caffeine metabolism, biosynthesis of phenylpropanoids, galactose metabolism and tyrosine metabolism, etc. Linustatin, scopoletin and phenylpropiolic acid were picked out from these DRMs and found to have suppressive activity against F. oxysporum through correlation analysis and antifungal experiments. The three DRMs showed strong inhibitory effects on the growth and spore germination of F. oxysporum at concentrations of 0.5 mM or higher in each test period. Furthermore, F. oxysporum showed a phobotaxis effect against these three DRMs at concentrations as low as 0.25 mM. Finally, we found that the three DRMs had an inhibitory effect on F. oxysporum by destroying the integrity of the cell membrane and increasing the membrane permeability of F. oxysporum. This study firstly reports the inhibition activity of phenylpropiolic acid and linustatin on F. oxysporum, providing a practical and environmentally friendly method for biocontrol of TFW by using natural fungicides.

Design, synthesis, and antifungal activity of novel cyanoacrylate derivatives containing a naphthalene moiety as potential myosin-5 inhibitor

In search of innovative antifungal solutions for the control of plant diseases, a series of cyanoacrylate derivatives containing naphthalene groups were designed and synthesized, and their inhibition activity against four plant pathogenic fungi was evaluated. The results of in vitro bioassay revealed that some target compounds possessed obvious antifungal effect against Fusarium graminearum. As the most prominent one, compound A2 showed a inhibition rate of 98.46 % at 10 µg/mL and an EC50 value of 0.26 µg/mL, which was close to that of the positive control phenamacril (with a inhibition rate of 100 % at 10 µg/mL and EC50 value of 0.14 µg/mL). The compound A2 also markedly inhibited the growth of F. graminearum inoculated on rice leaves at 200 μg/mL with the protective and curative efficiencies of 89.03 % and 90.91 %, respectively, which were close to that of the positive control phenamacril (with the protective and curative efficiencies of 94.54 % and 96.36 %, respectively). The observation under scanning electron microscopy and measurement of relative conductivity revealed that compound A2 caused the hyphal surface become shrunken and rough, and made the cell membrane permeability increased. Molecular docking and molecular dynamics simulation analyses showed that compound A2 interacted with the key residues in the active site of myosin-5 in a similar mode as phenamacril. These results suggested that target compounds were potential myosin-5 inhibitors, they could serve as the lead compounds for further structural optimization to develop new fungicides against F. graminearum.

Studies on a novel oxo-vanadium(V) complex of a tridentate ONO Schiff base ligand: Synthesis, characterization, X-ray crystal structure, Hirshfeld surface analysis, biological and catalytic activity

This study reports the successful synthesis and characterization of a novel oxovanadium(V) complex, [VO(L)(MeOH)(MeO)], prepared from 2-hydroxy-3-methoxybenzaldehyde and 2-methyl-3-aminoquinazoline. To elucidate the structure of the complex, we employed comprehensive characterization techniques such as CHN analysis, molar conductivity measurements, FT-IR, 1H NMR, UV-Vis spectroscopy, and single-crystal X-ray diffraction. The X-ray analysis confirmed an octahedral geometry around the V(V) center, coordinated with donor atoms from the deprotonated Schiff base ligand, an oxido group, a methanol molecule, and a methoxy group. Hirshfeld surface analysis was employed to evaluate intermolecular interactions.Furthermore, the complex exhibited impressively efficient catalytic activity in glucose oxidation under mild conditions (aqueous solution, room temperature, O2 oxidant), achieving a conversion rate of 98 %. Additionally, the antibacterial activity of the ligand and complex against various bacterial strains, including Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, and Bacillus cereus, was evaluated. The results demonstrated promising antibacterial potential of the [VO(L)(MeOH)(MeO)] complex, particularly against E. coli, P. aeruginosa, and B. cereus. These findings suggest potential applications of this new oxovanadium(V) complex in both catalysis and antibacterial treatments.

Synthesis and study of structural, electric, and dielectric behavior of La0.5Sm0.2Sr0.3Mn1-xFexO3 perovskite

In this study, the synthesized samples La0.5Sm0.2Sr0.3Mn1-xFexO3 (x = 0.05, 0.15 and 0.20) were thoroughly investigated for their crystalline structure, electrical conductivity, and dielectric properties, the samples were prepared using autocombustion method. According to the X-ray diffraction study, the samples crystallized in an orthorhombic symmetry with the Pnma space group. To measure the dielectric characteristics, impedance spectroscopy was conducted over the temperature range of 100–260 K and a frequency range of 100 Hz to 1 MHz. Measurements of AC conductivity are indeed utilized to investigate the transport properties of materials being studied. The results indicated that both temperature and frequency significantly influence the conduction process. Three theoretical hypotheses were proposed to explain the hopping conduction: overlapping large polaron tunneling (OLPT), the non-overlapping small polaron tunneling (NSPT) mechanism, and correlated barrier hopping (CBH). It is also shown that the conductivity diminishes with an increase in Fe content. La0.5Sm0.2Sr0.3Mn1-xFexO3 (x = 0.05, 0.15 and 0.20) can be used in electronic applications because of the high permittivity values confirmed by the dielectric measurements. With the aim of evaluating the distinct impacts of electrodes, grain boundaries, and grains on the complex impedance results, an appropriate alternative electrical circuit was utilized. Analysis of the sample's modulus indicated non-Debye characteristics and electrical relaxation phenomena. The materials exhibit good electrical properties, as well as strong chemical and thermal stability.

Biocontrol of rusted root rot in Panax ginseng by a combination of extracts from Bacillus amyloliquefaciens YY8 crude protein and Enterobacteriaceae YY115 ethyl acetate

BackgroundRusted root rot is one of the most common root diseases in Panax ginseng, and Cylindrocarpon destructans is one of the main pathogenic fungus. The objective of this study was to screen and explore the extracts of biocontrol bacteria isolated from ginseng rhizosphere soil against Cylindrocarpon destructans.ResultsBacterial strains Bacillus amyloliquefaciens YY8 and Enterobacteriacea YY115 were isolated and found to exhibit in vitro antifungal activity against C. destructans. A combination of crude protein extract from B. amyloliquefaciens YY8 and ethyl acetate extract from Enterobacteriacea YY115 in a 6:4 ratio exhibited the strongest antifungal activity against C. destructans. Measurements of electrical conductivity, protein content, and nucleic acid content in suspension cultures of C. destructans treated with a mixture extracts indicated that the extracts disrupted the cell membranes of rusted root rot mycelia, resulting in the leakage of electrolytes, proteins, and nucleic acids from the cells, and ultimately inhibiting the growth of C. destructans. The combined extracts suppressed the infection of ginseng roots discs by C. destructans effectively.ConclusionThe extracts obtained from the two bacterial strains effectively inhibited C. destructans in P. ginseng. It can provide scientific basis for the development of new biological control pesticides, reduce the use of chemical pesticides, and promote the sustainable development of agriculture.

Aggregation behavior of newly synthesized Gemini cationic surfactants in absence and in presence of different inorganic salts in 15% DMSO–water solvent

In this study, three Gemini cationic surfactants related to thiazol-2-amine with three hydrocarbon chain lengths including 3-hexylthiazol-3-ium (TAC6), 3-dodecylthiazol-3-ium (TAC12) and octadecylthiazol3-ium (TAC18) were prepared. Surfactant structures were confirmed with IR and 1HNMR Spectroscopies. Critical micelle concentrations for all surfactants in 15% DMSO-Water solvent were measured using conductometric, refractometric, and densitometric techniques. Thermodynamics parameters were computed and explained. Also, enhancing properties of all surfactants were indicated under the effect of two concentrations, 0.001 M and 0.01 M, of six inorganic salts including Cl−, Br−, I−, Co+2, Cu+2, and Mn+2 radicals using conductivity and refractive index measurements. All techniques used to measure critical micelles concentration showed a good convergence in measuring CMC values and the behavior of all surfactants in 15% DMSO-water solvent. Increasing the binding constant of the counter ion and association constant reflects the effect of hydrocarbon chain length increment on enhancing micelle formation, where TAC 18 was shown as the lowest CMC in all applied measurements. Modeling the density of all surfactant solutions under study indicates an increase in hydrophobic polarizability with an increase in the molecular weight of the surfactant. Inorganic salts decreased the CMC of all surfactants with the increase in Gibbs free energy of micellization which ensures easier formation of more stable micelles in the presence of a salt solution. The effect of salts on decreasing CMC for all surfactants under study was arranged in the following order: Mn+2 < Cu+2 < Co+2 for cationic radicals and I− < Br− < Cl− for anionic radicals.