Electron Microscopy Studies Research Articles

Unveiling the untapped potential of Hibiscus Rosa-sinensis lignocellulosic fiber: A multifaceted characterization for advancing sustainable biocomposite applications

In the pursuit of sustainable advancements in bio-inspired fiber reinforced polymer composite materials, the exploration of novel natural fibers has become a focal point of research. This experimental study aims to elucidate the unexplored potential of Hibiscus Rosa-sinensis fiber (HRF) as a versatile reinforcement material for high-performance composites. Through an integrated approach, this research offers a meticulous analysis of the HRF's physico-chemical properties, and single fiber tensile strength. The crystalline structure are revealed by X-ray diffraction (XRD), thermal behavior are characterized through thermo-gravimetric analysis (TGA), and surface morphology has been visualized using field emission scanning electron microscopy (FESEM) studies. From the results, it is found that the HRF contains a cellulose content of 79.50 %, positioning it as a prime bast fiber among its counterparts. This composition is complemented by hemicellulose (10.36 %), lignin (4.62 %), wax (0.84 %), and ash (2.96 %). The Fourier-transform infrared spectroscopy (FTIR) spectra unveils the intricate functional groups present in the fibers. XRD analysis highlights a crystallinity index (CI) of 66.93 %, confirming a well-organized and structured crystalline arrangement. The thermal stability established through TGA underscores HRF's resilience up to 284 °C, presenting it is an optimal reinforcement material for bio-inspired green composites operating within 280 °C. The surface morphology of HRF is examined through FESEM and three-dimensional profiling, showcasing its inherent morphological intricacies. The multidimensional characterization provided herein contributes significantly to the evolving landscape of biocomposite research, fostering a platform for future advancements and innovations in HRF-based composite materials.

Ultrastructural investigation of the posterior hyaloid membrane in posterior vitreous detachment.

Separation of the posterior hyaloid membrane (PHM) from the retina in posterior vitreous detachment (PVD) is a fundamental, but poorly understood, process underlying vitreoretinal disorders including retinal detachment and macular hole. We performed electron microscopy studies of the PHM after PVD to investigate its ultrastructure, associated cellular structures and relationship to the internal limiting membrane (ILM). Post-mortem human eyes were collected from recently deceased patients over 70 years of age. A posterior scleral button was trephined to identify PVD status, and the PHM and vitreous prepared for analysis with transmission and scanning electron microscopy. Twelve eyes from six patients were collected. Seven eyes had PVD; five eyes had attached vitreous. PHM was isolated from seven of seven eyes with PVD. The PHM in eyes with PVD is a laminar lacy sheet, distinct from the disorganised fibres of vitreous gel. Eyes without PVD had vitreous encased in internal limiting membrane which had separated en bloc from the retina. Cells embedded in the PHM (laminocytes) were identified in five of seven eyes with PVD, with strands stretching into the membrane. PHM isolated from eyes with PVD is distinct from artefactual separation of the ILM from the retina during dissection. PHM is ultrastructurally distinct from vitreous gel and is a separate entity. The en face appearance of PHM is similar to that of ILM, suggesting that in PVD, PHM forms from separation of an inner layer of ILM. Laminocytes may play a role in the pathogenesis of vitreoretinal disease.

Synthesis of low‐cost microporous activated carbon adsorbents for CO2 capture from Palmyra palm fruit shell waste biomass

AbstractUsing chemical activation techniques at dissimilar carbonization temperatures, activated carbon adsorbents were produced from Palmyra palm fruit biomass in this work. X‐ray diffraction, Fourier transform infrared spectroscopy, X‐ray photoelectron spectroscopy, laser Raman spectroscopy, scanning electron microscopy, CHNS‐elemental analysis, and N2 adsorption studies were among the characterization techniques used to assess the characteristics of the carbon adsorbents. The carbon adsorbents from Palmyra palm fruit were used to absorb CO2 in a temperature range of 25–70°C. The findings of the characterization showed that these carbons have a large surface area and microporosity. The temperature of carbonization and the activating agent had an impact on the surface characteristics. The samples with the highest adsorption capacity, 4.70 mmol/g at 25°C, were the activated carbons made by treating them with KOH and then carbonizing them at 750°C. The physicochemical properties of the adsorbents provided an explanation for their high adsorption capacity. The adsorbents showed simple desorption and maintained constant activity during ten cycles of recycling.

Investigation of Fibrillar Aggregates Formed by Pathogenic Pre-Pro-Vasopressin Mutants that Cause ADNDI.

Aggregations of unfolded or misfolded proteins, both inside and outside cells, are implicated in numerous diseases, collectively known as amyloidosis. Particularly, Autosomal dominant neurohypophyseal diabetes insipidus (ADNDI) is a rare disease caused by mutations in the AVP-NPII gene, leading to the inability to secrete arginine vasopressin (AVP). These misfolded proteins accumulate within the endoplasmic reticulum (ER), causing cellular dysfunction. This study aimed to investigate the formation of amyloid-like aggregates within the cell resulting from misfolded mutant precursor proteins, which induce disulfide-linked oligomers due to the G45C, 207_209delGGC, G88V, C98X, C104F, E108D-1, E108D-2 and R122H mutations identified by our group in the AVP-NPII gene of ADNDI patients. De-glycosylation studies were performed to analyze the glycosylation patterns of mutant protein precursors. The involvement of these precursors in the ER-related degradation pathway was studied by conducting protease inhibition experiments. Disulfide-linked oligomer analysis determined the oligomerization status of the mutant precursors. Immunofluorescence and electron microscopy studies provided evidence of aggregate structures in the ER lumen. In vitro studies involving bacterial expression and fibril formation in E. coli. Our findings demonstrated that the N-glycan structure of mutant precursors remains intact within the ER. Protease inhibition experiments indicated the involvement of these precursors in the ER-related degradation pathway. Disulfide-linked oligomer analysis revealed homo-oligomer structures in mutations. Immunofluorescence and electron microscopy studies confirmed the presence of aggregate structures in the ER lumen. In vitro studies showed that mutant precursors could form fibril structures in E. coli. Our study may support the idea that ADNDI belongs to the group of neurodegenerative diseases due to the formation of fibrillar amyloid aggregates in the cell.

Covalent Carbide Interconnects Enable Robust Interfaces and Thin SEI for Graphite Anode Stability under Extreme Fast Charging.

Carbonaceous and carbon-coated electrodes are ubiquitous in electrochemical energy storage and conversion technologies due to their electrochemical stability, lightweight nature, and relatively low cost. However, traditional reliance on conductive additives and binders leads to impermanent electrical pathways. Here, a general approach is presented to fabricate robust electrodes with a progressive failure mechanism by introducing carbide-based interconnects grown via carbothermal conversion of (5 wt%) titanium hydride nanoparticles. This method concurrently enhances both electrical and mechanical properties within the electrode architecture. The resulting chemical bonding between active materials establishes a novel mechanism to maintain stable electrical pathways during cycling. Employed as Li-ion battery anodes, these electrodes exhibit improved cyclability, achieving 80% capacity retention after 800 fast-charge cycles at moderate loading (1 mAh cm- 2). High loading cells with areal capacity of 3 mAh cm-2 show significantly improved cycle lifeover the same number of cycles. This performance improvement is attributed to the absence of significant impedance growth and a thinner solid electrolyte interphase (SEI) layer formed at high current densities (4C) as demonstrated by X-ray photoelectron spectroscopy and transmission electron microscopy studies. The enhanced conductivity facilitates SEI formation, lowering ionic impedance and mitigating lithium plating, ultimately leading to the reported extended cycle life.

Structure and sexual dimorphism of the first antennae in Penaeus vannamei, Boone, 1931

ABSTRACT This contribution is a histological and scanning electron microscopy study of major flagellar setae of antennules from the most cultured crustacean species, Penaeus vannamei. Antennule samples were collected from females and males of selected species and processed for histological as well as scanning electron microscopy (SEM) evaluation. The histological and SEM description of major setae from antennules, namely aesthetascs, plumose setae, and male spines are presented in detail. A unique sexually dimorphic structure, male spines on the inner (medial) flagella, is reported for the first time in a penaeid shrimp. These spines are robust structures, short and thick with non-permeable cuticle and no terminal pore, innervated by receptor neuron clusters. This histological organization suggests the spines are sensilla for mechanoreception, possibly involved in courtship mechanoreception, complementing chemosensory information from aesthetascs. Additionally, SEM observations of other antennule setae are presented, including asymmetric setae associated with aesthetascs.

Eggshell bio-derived hydroxyapatite particle-wool/polyester staple fibers hybrid reinforced epoxy bio-composites for biomedical services

This study assessed the impact of hybrid reinforcement from natural and synthetic materials on the wear and mechanical properties of epoxy-based composite materials needed for biomedical applications. Hydroxyapatite was synthesized from eggshells using the hydrothermal method, while wool fiber was obtained from cow hair. The hybrid reinforced composites were developed by blending hydroxyapatite particles and the fibers by hand layup method in an open mold production process, with specified amounts of 3–15 wt % reinforcement. The characterized properties included tensile and flexural strengths, impact energy, wear resistance, and hardness. A scanning electron microscopy study was conducted to analyze the adhesion between the matrix and reinforcements at the interface, providing valuable insights into the overall integrity of the composites. The results showed a significant increase in the properties of the hybrid reinforced composites when compared with the pristine sample. In particular, the 6 wt% reinforced composite enhanced 61.14 % in tensile strength and 160.79 % enhanced 61.14 % in tensile strength and 160.79 % in flexural strength. Thus, the study shows that substituting synthetic fibers with hybrid organic-based reinforcement offers a viable approach for developing sustainable materials with improved mechanical properties suitable for biomedical applications.

Development of a selective COX-2 inhibitor: from synthesis to enhanced efficacy via nano-formulation.

Non-steroidal anti-inflammatory drugs NSAIDs are widely used for managing various conditions including pain, inflammation, arthritis and many musculoskeletal disorders. NSAIDs exert their biological effects by inhibiting the cyclooxygenase (COX) enzyme, which has two main isoforms COX-1 and COX-2. The COX-2 isoform is believed to be directly related to inflammation. Based on structure-activity relationship (SAR) studies of known selective COX-2 inhibitors, our aim is to design and synthesize a novel series of 2-benzamido-N-(4-substituted phenyl)thiophene-3-carboxamide derivatives. These derivatives are intended to be selective COX-2 inhibitors through structural modification of diclofenac and celecoxib. The compound 2-benzamido-5-ethyl-N-(4-fluorophenyl)thiophene-3-carboxamide VIIa demonstrated selective COX-2 inhibition with an IC50 value of 0.29 μM and a selectivity index 67.24. This is compared to celecoxib, which has an IC50 value of 0.42 μM and a selectivity index 33.8. Molecular docking studies for compound VIIa displayed high binding affinity toward COX-2. Additionally, the suppression of protein denaturation with respect to albumin was performed as an indicative measure of the potential anti-inflammatory efficacy of the novel compounds. Compound VIIa showed potent anti-inflammatory activity with 93% inhibition and an IC50 value 0.54 μM. In comparison, celecoxib achieved 94% inhibition with an IC50 value 0.89 μM. Although molecule VIIa demonstrated significant in vitro anti-inflammatory activity, adhered to Lipinski's "five rules" (RO5) and exhibited promising drug-like properties, it showed indications of poor in vivo activity. This limitation is likely due to poor aqueous solubility, which impacts its bioavailability. This issue could be addressed by incorporating the drug in niosomal nanocarrier. Niosomes were prepared using the thin-film hydration technique. These niosomes exhibited a particle size of less than 200 nm, high entrapment efficiency, and an appropriate drug loading percentage. Transmission electron microscopy (TEM) and differential scanning calorimetry (DSC) studies revealed that the niosomes were spherical and demonstrated compatibility of all of its components. The drug release study indicated that the pure drug had limited practicality for in vivo use. However, incorporating the drug into niosomes significantly improved its release profile, making it more suitable for practical use.

Achieving the 1D Atomic Chain Limit in Van der Waals Crystals.

Experiments with graphene have demonstrated that 2D van der Waals materials can be stable, robust, and efficiently manipulated at the level of individual atomic planes. However, the stability and manipulation of 1D van der Waals materials and individual atomic chains remains elusive. Here, the ability to exfoliate and process two representative van der Waals materials containing 1D motifs, namely MoI3 and Ta2Se8I, at the scale of individual atomic chains is demonstrated. High-resolution transmission electron microscopy and atomic force microscopy studies confirm the presence of stable individual atomic chains of MoI3 at room temperature. It is further shown that 1D van der Waals materials with low exfoliation energy, such as Ta2Se8I, can be processed with electron beams to achieve suspended individual atomic chains. Ab initio calculations corroborate the findings regarding the cleavage energies and the thermodynamic stability of individual atomic chains in these 1D van der Waals materials. These results demonstrate that the top-down approach in material processing can be extended to the scale of individual chains.

Cytocompatible Hyperbranched Polyesters Capable of Altering the Ca2+ Signaling in Neuronal Cells In Vitro.

Synthetic hyperbranched polyesters with potential therapeutic properties were synthesized using the bifunctional polyethylene glycol or PEG with different molecular weights, ca., 4000, 6000, and 20,000 g/mol, and the trifunctional trans-aconitic acid or TAA. During polycondensation, a fixed amount of PEG was allowed to react with varying amounts of TAA (1:1 and 1:3) to control the branching extents. It was found that the synthetic polyesters had a considerable yield and were highly water soluble. Spectroscopic data (Fourier transform infrared and 1H NMR) confirmed the polyester formation; the branching percentages were determined from 1H NMR spectroscopy which varied from 73% to 22% among the synthesized samples. As the molecular weight of PEG was increased, the branching percentage drastically dropped. All polyesters were found to be negatively charged due to the ionization of unreacted -COOH in the branched ends at the working pH (7.4). Both the hydrodynamic size and intrinsic viscosity were found to reduce as the branching extent increased. Among the sets of polyesters, the one with the highest branching percentage (73%) showed the core-shell morphology (evident from field emission scanning electron microscopy and transmission electron microscopy studies). It also exhibited the highest efficiency toward Ca2+ influx in neuronal cells due to the unique morphology and the negatively charged surface. Nevertheless, this particular grade of polyester along with all the other grades was cytocompatible and induced reactive oxygen species generation. Since the maximally branched grade was highly efficient in altering the Ca2+ signaling through stronger influx, it may well be tested for treating neuronal disorders in vivo in future.

Synthesis of a dehydrodieugenol B derivative as a lead compound for visceral leishmaniasis-mechanism of action and in vivo pharmacokinetic studies.

Leishmaniasis is a parasitic neglected tropical disease, affecting 12 million people. Available treatments present several limitations, with an increasing number of resistance cases. In the search for new chemotherapies, the natural product dehydrodieugenol B was used as a scaffold for the synthesis of a series of derivatives, resulting in the discovery of the promising analog [4-(4-(5-allyl-3-methoxy-2-((4-methoxybenzyl)oxy)phenoxy)-3-methoxybenzyl)morpholine, 1]. In this work, we investigated the effect of compound 1 on cell signaling in Leishmania (L.) infantum, culminating in cell death, as well as its immunomodulatory effect in the host cell. Additionally, we performed a pharmacokinetic profile study in an animal model. After treatment, compound 1 induced the alkalinization of acidocalcisomes and concomitant Ca2+ release in the parasite. These events may induce depolarization of the mitochondrial potential, with successive collapse of the bioenergetic system, leading to a reduction of ATP and reactive oxygen species (ROS) levels. The analysis of total proteins and protein profile by matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF/MS) demonstrated that compound 1 also altered the parasite proteins after treatment. Transmission electron microscopy studies revealed ultrastructural damage to mitochondria; together, these data suggest that compound 1 may promote autophagic cell death. Additionally, compound 1 also induced an immunomodulatory effect in host cells, with a reduction of Th1 and Th2 cytokine response, characterizing an anti-inflammatory compound. The obtained pharmacokinetic profile in rats enhances the potential of the compound, with a mean plasma half-life (T1/2) of 21 h. These data reinforce the potential of compound 1 as a new lead for future efficacy studies.

Ultrastructural Characterization of Testis in Non-descript Goat (Capra hircus)

Background: The proposed experiment was aimed at locating the spermatogonial stem cell niches inside the testis and to characterise the development of germ cells of testis in the non- descript goats at the different stages of pre and post natal life, which could be useful in selecting the goats for breeding at appropriate time and for other interventions related to reproductive developments in the goats. Methods: The present study was conducted on the testes of non-descript goats divided into three groups, viz. neonatal (within 1 month), prepubertal (from 1-18 months) and pubertal (above 18 months) with 10 healthy animals in each group. The collected samples of testis were processed for scanning electron microscopic study and subsequently, the samples were viewed and the photographs were taken in the facility available at Central Instrumentation Facility (CIF), OUAT, Bhubaneswar. Result: The present study revealed that the testis was surrounded by the tunica albuginea, a thin capsule of connective tissue, from which thin septum originated and extended into the inside of the organ. Among these septa, the seminiferous tubules were found. The seminiferous epithelium consisted of spermatogonial cells at different stages of development separated from each other by interstitial connective tissue. The interstitium was made up of randomly arranged collagen bundles. The intertubular vascular connective tissue contained Leydig cells mainly at wider locations where they were bounded by more than two seminiferous tubules. The mediastinal rete testis area contained many cavities of many intercommunicating channels supported by connective tissue pillars. The present study helped in developing a baseline data on the ultrastructural characteristics of seminiferous epithelium, rete restis, peritubular cells, Lyedig cells and other components of testis in non-descript goat at different post natal stages under study. The appearance of seprmatogonial cell lineage at the various post natal stages in non-descript goat would help in accessing the reproductive status of the animal.

Electrochemical, gravimetric and surface studies of Phalaris canariensis oil extract as corrosion inhibitor for 316 L type stainless steel in H2O-LiCl mixtures

The corrosion inhibition action of Phalaris canariensis extract on 316 L stainless steel in the H2O-35 (wt%) LiCl mixture at different temperatures has been evaluated with the aid of weight loss, potentiodynamic polarization curves, linear polarization resistance and electrochemical impedance spectroscopy tests. These studies were complemented by Fourier Transformed Infrared spectroscopy, FTIR, gas/mass chromatography analytical techniques and detailed scanning electronic microscopy studies. Results have indicated that Phalaris canariensis extract is an efficient inhibitor, with an efficiency that increases with its concentration, but it decreases as the temperature increases. Phalaris canariensis extract is physically adsorbed onto stainless steel according to a Temkin type of adsorption isotherm. Phalaris canariensis extract affected both anodic and cathodic electrochemical reactions with a stronger effect on the anodic ones, acting, thus, as a mixed type of inhibitor. Main compounds contained in the Phalaris canariensis extract were palmitic and oleic acids, responsible for its inhibitory properties.

High Temperature, Isothermal Growth Promotes Close Packing and Thermal Stability in DNA-Engineered Colloidal Crystals.

We report a strategy to accelerate the synthesis and increase the crystallinity of colloidal crystals (CCs) engineered with DNA. Specifically, by holding the DNA-modified Au particle building blocks above the Tm of the DNA bonding elements (i.e., free from the particles), but slightly below the Tm of the anticipated CC during the assembly process, crystallinity is increased, and enthalpically favored phases with high degrees of facet registration are observed. We studied the utility of this approach with systems for which the commonly adopted slow-cooling approach yielded primarily amorphous aggregates. In particular, we used it to synthesize high-volume fraction CCs from large (80 nm) anisotropic nanoparticles (cubes and rhombic dodecahedra) with short (<14 nm) DNA designed to restrict the degrees of freedom for the DNA bonds and maintain the anisotropy of the particle building block. Small-angle X-ray scattering and electron microscopy studies show that the crystalline phases synthesized via this method are more thermally stable than their corresponding aggregate phases, likely due to an increased number of DNA-DNA bonds between particles. Crystal size tunability (between 0.5 and 15 μm edge lengths) and epitaxial growth were demonstrated using this strategy by modulating the NaCl concentration in tandem with previously synthesized CC nuclei. Taken together, this isothermal strategy demonstrates how to deliberately crystallize a wide variety of anisotropic colloidal materials and expands the phase space accessible to nanoparticles modified with DNA.

Er3+/Tm3+ codoped CaF2 based oxyfluoroborosilicate glass-ceramics for fiber laser applications

Transparent Er3+/Tm3+ codoped CaF2 based oxyfluoroborosilicate glass-ceramics (BSEr1TmxGCs) with variable Tm3+ concentration were prepared through melt quench process followed by reheat treatment at 450 °C/1h. They were characterized through differential scanning calorimetry (DSC), powder X-ray diffraction (XRD), Fourier transform infrared (FTIR) Raman spectroscopy, near infrared (NIR) emission and luminescence decay. The formation of CaF2 nanocrystallites against oxyfluoroborosilicate glassy phase was confirmed by scanning electron microscopic (SEM) and hi-resolution transmission electron microscopic (HRTEM) studies. The NIR emission properties were investigated at 460 nm diode laser pumping. The applicability of BSEr1TmxGCs were examined by evaluating effective bandwidth (Δλeff), stimulated emission cross-section (σe), gain bandwidth (σe × Δλeff), figure of merit (σe × τR) and quantum efficiency (ηQE). The energy transfer efficiency (ηET), rate of energy transfer (WET) between Er3+ and Tm3+ and the rate of non-radiative transitions (WNR) were also calculated. The comparative NIR emission performance suggests that the BSEr1Tm1GC has proficiency for 1530 nm broadband fiber lasers and optical amplifiers in short wavelength and conventional wavelength (S + C) band communication window.

Tunable Charge Transport Using Heterocycles-Flanked Alkoxyphenanthrenes for High-Performing OFETs.

A series of new heterocycles-flanked alkoxyphenanthrenes with D'-D-D' and A-D-A architecture was synthesized for high-performance solution-processable p-channel, n-channel, and ambipolar organic field-effect transistors. The impact of electron-donating and -accepting abilities of the sulfur- and nitrogen-containing heteroaromatics on photophysical, electrochemical, and semiconducting properties was analyzed. The presence of heteroaryl rings improves the extended conjugation, two-dimensional lattices of π-π stacks, and increased molecular interaction of the functionalized phenanthrenes (PN) to allow better self-assembly. The electronically dynamic PN self-assembles into continuous microdomains, forming percolation channels for holes, electrons, or both reliant on functionalization. The low-lying LUMO levels of the compounds enabled ambipolar transport and reduced energy levels for charge injections. Spin-coated devices fabricated using functionalized PN with sulfur-containing heteroaryl substituted PN exhibited the highest hole mobility of 0.85 cm2/(V s) with 108 on/off current ratio. Compounds with A-D-A architecture showed n-channel/ambipolar charge transport, especially napthalimide acceptor substituted PN exhibited n-channel electron mobility of 0.78 cm2/(V s) and an on/off ratio of 106. X-ray diffraction and scanning electron microscopy studies further delineate the impact of efficient packing in the film. Quantum chemistry calculations combined with Marcus-Hush electron transfer theory interpret the transport parameters, and heteroatoms are established to impact the charge mobility intensely.

Tailoring of magnetic phase: Co-doped SiC thin films grown by RF sputtering

In the present work, we investigate the influence of cobalt (Co) doping on the structural and magnetic properties of cobalt-doped silicon carbide (Co-SiC) thin films. The films were fabricated using DC/RF magnetron sputtering technique on Si (100) substrates at a temperature of 1200°C, with varying Co concentrations ranging from 5 to 16 at. (at%. X-ray diffraction (XRD) analysis unveiled the co-existence of CoSi2 and SiC phases in all the thin films. Surface morphological study through atomic force microscopy (AFM) revealed the densely packed nature of the films. Field emission scanning electron microscopy (FE-SEM) study showed that particles are uniformly distributed at the surface of the substrate. According to UV measurements, the films have high transmittance in the visible range, and as Co concentration rises, transmittance decreases. A magnetic phase transition from superparamagnetic to ferromagnetic behavior occurred with Co content surpassing 8 at% in the SiC thin films. Moreover, an increase in coercivity was observed from 38 Oe to 316 Oe as the doping concentration increased from 10 to 16 at%. This study represents an exploration into the induction of ferromagnetism through moderate Co doping in SiC thin films.

Effect of pH on the microstructure and antibacterial properties of MgO nanoparticles by microwave-assisted solution combustion

The application of magnesium oxide (MgO) nanoparticles as a candidate material for antibacterial purposes has been limited by their relatively low antibacterial activity. In this study, antibacterial MgO nanoparticles were synthesised in one step using magnesium nitrate and citric acid as raw materials using an economical and environmentally friendly microwave-assisted solution combustion approach, while the effect of the pH of the reaction system (2, 4, and 7) on the structure and antimicrobial properties of the synthesised MgO nanoparticles was investigated. X-ray diffraction (XRD) analysis demonstrated the formation of cubic-phase MgO nanoparticles, and electron microscopy studies confirmed that MgO nanoparticles synthesised at a precursor solution pH of 4 had uniform size distribution with a small microcrystalline size (∼19 nm) and spherical granular morphology. In addition, the results of the plate colony counting method showed that the antibacterial rate of MgO-4 against Gram-negative Escherichia coli (106 CFU/mL) at a sample concentration of 100 μg/mL was as high as 99.86 %, which showed excellent antibacterial performance. These findings provide valuable insights into how to increase the degree of oxygen adsorption on the sample surface to participate in the reaction, as well as a potential method for constructing nanomaterials with high antimicrobial activity.

SYNTHESIS AND PHYSICO-CHEMICAL PROPERTIES OF A NEW COMPLEX FERRITE

The article discusses the synthesis of new complex ferrite, radiographic and electron microscopic studies. The phase of complex ferrites was synthesized by the method of high-temperature sol-gel synthesis. For the first time, the structure of CrKFe2O5 Composite ferrite was studied by X-ray phase analysis and scanning electron microscope methods, the syngony type, elementary cell parameters, radiographic and pycnometric densities, and elemental analysis were determined. A comparative analysis of the relationship between the parameters of the Crystal cell of primary substances and the parameters of the obtained complex ferrite Crystal cell was carried out. Micro-samples were taken from different parts of the crystallite obtained through a scanning electron microscope, the elemental composition of the crystals was analyzed, and the general type of layer of the complex ferrite surface was demonstrated. As a result, the fact that the compound consists of two phases, the clarity of its construction was determined by the topography and chemical composition of the compound. As a result, it was found that the newly synthesized complex ferrite corresponds to the Formula CrKFe2O5. The particle size of the compounds formed is large (between 200 μm, 20.0 μm, 5.00 μm and 2.00 μm).

Approach to Design Sustainable Alkali-Activated Slag Recycled Aggregate Concrete: Mechanical and Microstructural Characterization

There is a steep increase in demand for concrete as the need for infrastructure is increasing with a rapid increase in urbanization. Consequently, there has been a surging demand for cement across the globe. By using alkaline concrete activated with ground granulated blast furnace slag (GGBS), cement usage can be eliminated in concrete, which addresses the issue of CO2 emissions concerned with the cement manufacturing process and promotes the use of industrial by-products as sustainable building materials. The current study focuses on proposing a methodology to design sustainable GGBS-based alkali-activated concrete incorporated with 100% coarse recycled coarse aggregates (RCA) recovered from construction and demolition (C&D), for various strengths by optimizing the mix proportions and verifying the same through experiments. From the current study, it is evident that this mix design procedure can be adopted to design alkali-activated slag recycled aggregate concrete (AASRAC) mixes for strengths ranging from 44MPa to 85MPa. The optimum values of alkalinity factor (λ) and NaOH concentration (M) i.e., 1.5 and 12, have a significant role in the development of high strengths which is attributed to the formation of hydrotalcite. Micrographs captured using scanning electron microscope (SEM) and energy dispersive X-ray spectroscopy (EDS) studies reveal that the alkaline binders promote the development of a denser and stronger interfacial transition zone (ITZ) that enhances the strength of lower AA/B concretes at the microstructural level as Ca/Si ratio is higher for lower AA/B concretes. Global warming potential (GWP) analysis reveals that the alkali-activated concretes have significantly lower GWP compared to conventional OPC-based concrete by approximately 2.5 times. The mix-design chart proposed in this study may pave the way to designing structural grade AASRAC with enhanced performance for the desired strength, which may find its application in fast-track construction and manufacturing of prefabricated elements.