Scanning Electron Microscopy Images Research Articles

Assessment of Bryophyllum pinnatum mediated Ag and ZnO nanoparticles as efficient antimicrobial and cytotoxic agent.

Bryophyllum pinnatum is used to cure infections worldwide. Although the flavonoids of this plant are well known, it is still unknown how much of the plant's Ag and ZnO nanoparticles are beneficial. In the current research work, silver and zinc oxide nanoparticles were prepared using Bryophyllum pinnatum extract. The synthesized particles were characterized by UV-visible spectroscopy, SEM, EDS, XRD and FTIR. Synthesized particles were subjected to evaluation of their bactericidal and antifungal activity at various doses. Uv vis spectra at 400nm corresponding to AgNPs confirmed their synthesis. Strong peaks in the EDS spectra of Ag and ZnO indicate the purity of the sample. The scanning electron microscopic images of ZnONPs showed a size of about 60nm ± 3nm, which demonstrated the presence of triangular-shaped ZnO nanoparticles. Green synthesized nanoparticles showed bactericidal activity against both Gram-positive (Micrococcus luteus, Staphylococcus aureus, Bacillus subtilis) and Gram-negative (Agrobacterium tumifaciens, Salmonella setubal, Enterobacter aerogenes) strains. AgNPs proved to be more effective against Gram-negative bacterial strains compared to Gram-positive owing to MIC values (10 ppm and 20 ppm respectively). Whereas, ZnONPs were found more effective against Gram-positive bacteria with lower MIC values (10 ppm) as compared to Gram-negative ones (20 ppm). Also, the synthesized nanoparticles exhibited moderate dose-dependent antifungal activity against tested fungal strains ranging from 10 to 70%. Cytotoxicity of nanoparticles was found significant using Brine shrimp's lethality assay with IC50 values of 4.09 ppm for AgNPs, 13.72 ppm for ZnONPs, and 24.83 ppm for plant extract. Conclusively, Ag and ZnO nanoparticles were more effective than plant extract and AgNPs had higher activities than those of ZnONPs. Further research is warranted to explore the precise mechanism of action and the potential applications of these nanoparticles in the medical field.

Assessing polylactic acid nanofibers with cellulose and chitosan nanocapsules loaded with chamomile extract for treating gram-negative infections.

This study presents the development and characterization of a novel nanocomposite wound dressing material based on polylactic acid (PLA) nanofibers incorporating chitosan nanocapsules loaded with chamomile extract and cellulose nanoparticles. The nanofibers were fabricated using a three-step synthesis and electrospinning techniques, resulting in uniform, bead-free fibers with an average diameter of 186 ± 56nm. Fourier-transform infrared spectroscopy confirmed the successful incorporation of all components, while tensile strength tests demonstrated improved mechanical properties by adding nanoparticles. Water contact angle measurements revealed enhanced surface wettability of the PLA-Cellulose-Chitosan complex compared to pure PLA nanofibers. In vitro biocompatibility assessments using MTT assays showed excellent cell viability and proliferation, with the optimized composite exhibiting the best performance. Scanning electron microscopy imaging confirmed robust cell adhesion and interaction with the nanofibers. The nanocomposite demonstrated significant antimicrobial activity against Escherichia coli, with a 20mm inhibition zone observed for chamomile extract-loaded samples. Additionally, the material showed superior hemostatic ability compared to commercial gauze and high hemocompatibility. These comprehensive results indicate that the developed nanocomposite is a promising candidate for advanced wound management applications, offering a multifunctional approach to wound healing by combining antimicrobial activity, cell compatibility, and hemostatic properties.

Feasibility study of utilizing Autoclaved Aerated Concrete (AAC) waste for the production of cold bonded lightweight artificial aggregate using high volume fly ash (HVFA) binders

Autoclaved Aerated Concrete (AAC) is a popular construction material used for partitions and insulation in buildings. At the end of its service life, AAC (Autoclaved Aerated Concrete) will be demolished and subsequently disposed of in landfills, thereby creating depository problem. Therefore, the study of reutilization and recycling of AAC waste is imperative. Artificial aggregate production can be an alternative to the reutilization of AAC waste. This paper assesses the feasibility of using Autoclaved Aerated Concrete Powder (AACP) waste as a raw material for the production of artificial aggregate and investigate its physico-mechanical properties. The investigation incorporates the comparison of cement-based binder with high-volume fly ash (HVFA) binder with different replacement levels of cement. The study uses image analysis based on photographic, optical microscopic, and scanning electron microscopy (SEM) images, to describe the porosity of the aggregate. The results show that the AACP aggregates with both cement and HVFA binders meets the current industry requirement for density and cylinder crushing strength as lightweight artificial aggregate. The appropriate binder content lies between 30 % and 40 %. The best cement to fly ash ratio in HVFA binder is determined to be of 1:1 with 50 % replacement of cement with fly ash. Image analysis showed that the porosity largely affected the properties of the AACP aggregate such as density and water absorption. However, further investigation into the reducing high-water absorption of AACP aggregates is necessary to improve their overall quality.

Application of Calcium Hypochlorite for Sanitizing 3/16-Inch Tubing Used in Maple Sap Collection.

Despite the widespread empirical adoption of calcium hypochlorite (Ca(ClO)2) for sanitizing 3/16-inch tubing after the maple sap collection season, there remains a dearth of scientific data on its best practice and effectiveness. To address this gap, we cultivated microbial mass in tubing through continuous maple sap flow at 7 °C for 5 weeks in the lab. The tubing was sanitized with 200, 400, or 600 ppm Ca(ClO)2 and retained Ca(ClO)2 for either 10 min, 1 h, 7 days, or 6 weeks. Half of the tubing segments underwent microbial analysis, while the other half were stored for 6 weeks post-flushing of the Ca(ClO)2 to determine microbial survival/growth. The level and presence of the microbial load were determined, and the inner tubing surfaces were visualized using scanning electron microscopy (SEM). The initial microbial load in the tubing was approximately 4-5 log CFU/cm2. A 10-min and 1 h contact time with 200 ppm Ca(ClO)2, and a 10-min exposure to 400 ppm Ca(ClO)2, achieved reductions of 2.4-2.8 log for Pseudomonas spp., 1.6-2.5 log for mold and yeast, and 2.3-3.3 log for psychrotrophic microorganisms. Microorganisms were recovered from the enrichment process after retaining 200 ppm Ca(ClO)2 for 6 weeks, indicating insufficient inactivation. Consequently, the data suggests the use of at least 400 ppm Ca(ClO)2 for 1 day. The SEM images supported the microbial count results, offering valuable insights for educating maple syrup producers on optimal tubing sanitation practices.

The change rule of lipid oxidation and hydrolysis driven via water in Antarctic krill oil: Based on association colloid formation

The residual water and amphiphilic compounds such as phospholipids in bulk oil can form reverse micelles, which affect oxidative stability. In this study, the Antarctic krill oil (AKO) samples with different water contents were subjected to accelerated storage. During storage, AKO exhibited oxidative changes, manifested as increased POV, TBARS values, and volatile compound levels but decreased PUFA percentages. Meanwhile, AKO underwent hydrolysis, evidenced by decreased PC, PE, and TG contents but increased FFA contents. Moreover, the degree of lipid oxidation and hydrolysis is dose-dependent with water added. Cryogenic scanning electron microscopy imaging and micelle size distribution measurement proved the presence of reverse micelle, and their size and interfacial area improved with increased water contents. Correlation analysis suggested that lipid oxidation and hydrolysis positively correlated with the size and interfacial area of reverse micelle. Therefore, it is speculated that the oil-water interface may be the site of lipid oxidation and hydrolysis.

Elucidating the effects of metal transfer modes and investigating the material properties in wire-arc additive manufacturing (WAAM)

AbstractStudies have shown the influence of WAAM process parameters on mechanical properties, bead formation, dimensional accuracy, and microstructure. However, metal transfer modes and their interactions with input variables have not been investigated thoroughly. Therefore, short/spray, pulse and double pulse modes were investigated in this study at different current levels. Bead-on-plate trials were conducted by depositing ER70S-6 wire to investigate bead morphology, dilution, microstructure, and hardness. The study was supported by a detailed statistical approach, including analysis of variance (ANOVA) and regression analysis. Similarly, the combined effects of hatch distance and current were studied on bead formation in multi-layer deposits. Moreover, a thin wall and a cubic structure were deposited to realize the WAAM capability for larger depositions. The microstructures of thin wall and cubic structure were analyzed using optical microscopy (OM) and scanning electron microscopy (SEM). The study concludes that metal transfer modes at various currents significantly influence bead geometry, microstructure and hardness. The microstructure of bead-on-plate trials show fine lamellar structure at low current in all modes. Higher current results in coarse grains with a polygonal and columnar morphology. The hardness shows a decreasing trend as the current increases. The combined effects of current and hatch distance alter bead morphology; however, an optimized combination yields smoother surfaces. The microstructure of thin wall showed a slight anisotropy along the building direction. The presence of small pores was witnessed from OM and SEM images. Similarly, the cubic structure showed a more homogeneous microstructure with much lower porosity. The hardness profile of the thin wall exhibited small fluctuations along the building direction, while that of the cubic structure was more uniform.

Exploring Digital Zoom in Scanning Electron Microscopy

Abstract The concept of zoom in scanning electron microscopy (SEM) once referred to increasing the magnification of the sample by reducing the scanned field size. However, with the introduction of digital technology, the concept of zooming has become a little more complicated. Historically, older SEMs operated at a 512 × 512-pixel lateral resolution (262 kB pixel density) at TV scan rates. Today's newest SEMs can achieve up to 32k × 24k (4:3 ratio) pixel lateral resolution, equating to an 805 MB pixel density. In this article, we explore the factors involved in selecting an appropriate frame grabber size for SEM imaging. Specifically, we will delve into the implications of pixel density, including its impact on digital zoom capabilities, image file sizes, and overall image acquisition times.

Characterisation Analysis of Sulphur and Phosphorous Doped and Co-doped Graphitic Carbon Nitride (g-C3N4) Materials

Graphitic carbon nitride (g-C3N4) is tailored with doping of different non-metals (Sulphur and Phosphorus). For synthesis through thermal condensation method, the mixtures of urea and dopant with diverse concentrations have been added for preparation of materials. The basic effect of doping and its concentration on the structural morphology and absorption spectra of the samples is investigated in detail. Pure g-C3N4 suffers from high recombination rate of photogenerated electron-hole pairs resulting in low photocatalytic activity. Different techniques like X-ray diffraction (XRD), Scanning electron microscopy (SEM), Fourier transforms infrared (FTIR) spectroscopy, and Photoluminescence spectroscopy (PL) have been used for the characterization. X-ray diffraction studies confirm the formation of the g-C3N4 structure and SEM images reveal crumpled sheets and irregular plate like shapes of the doped graphitic nitride samples. FTIR analysis identify the presence of surface amino (N-H) and water (O-H) groups, cyano terminal group (C≡N), (C≡C), C–N) and (C=N) bonds and breathing mode of the tri-s-triazine units in the samples. PL spectra shows that the sulphur and phosphorus co-doped PSGCN (8 wt.%) sample is better for photocatalytic activity.

Optimizing bioencapsulation of yeast cells by Aspergillus tubingensis TSIP9 and applications in bioethanol production through repeated-batch fermentation

This study aimed to immobilize yeast cells using filamentous fungi owing to a number of advantages including less chemical usage, spontaneous encapsulation, strong adhesion and biocompatibility. Filamentous fungus, Aspergillus tubingensis TSIP9 could form sphere-shape and packed pellets using either fungal fresh spores or those stored in liquid medium for 6 weeks at 4 °C. The fungus was used to immobilize yeast Saccharomyces cerevisiae FAI via adsorption and co-cultivation methods. Scanning electron microscopy images revealed that the bioencapsulated yeast cells via co-cultivation seemed to be more tightly adhered on fungal mycelia and surrounded by extracellular polymeric substances. The yeast biocapsules also exhibited higher stability and maintained their structural integrity during repeated-batch fermentation while the immobilized yeast cells by adsorption gradually degraded during their repeated uses. The bioethanol production from glucose by yeast biocapsules were in the range of 95–98 g/L with the bioethanol yield of 0.49–0.54 g-ethanol/g-consumed glucose. The yeast biocapsules could produce bioethanol well when using enzymatic hydrolysate of lignocellulosic palm waste, as alternative cheap carbon source, with the comparable bioethanol yield of 0.49 ± 0.17 g-ethanol/g-consumed glucose. The spontaneous and inter-species bioencapsulation show the perspectives as active biocatalysts with high cell retention for repeated uses.

Reevaluation of pollen differentiation in Altingiaceae: Challenges in distinguishing deciduous (Liquidambar) and evergreen (Altingia) types using multivariate statistics and machine learning

Altingiaceae, a family of woody plants, comprising evergreen Altingia and deciduous Liquidambar groups, exhibits distinct leaf morphology, yet both groups overlap in geographical range and climatic conditions. While some tropical Altingia species are confined to Myanmar, Thailand, Cambodia and India without Liquidambar, and some temperate Liquidambar species to northern China without Altingia. Their fossil pollen have significant implications in reconstructing palaeoclimate and historical biogeography, based on classification of Altingia-type and Liquidambar-type. However, the results of previous studies to differentiate pollen types of evergreen Altingia and deciduous Liquidambar were based on limited pollen specimens. Therefore pollen morphology of Altingiaceae and differentiation of above mentioned types needs reevaluation using more specimens from wider geographical range.In this study, we present new findings on Altingiaceae pollen morphology from extensive collection of specimens and reassess the diagnostic features to distinguish evergreen and deciduous types. To improve the credibility of palaeoecological and palaeoclimatic interpretations, we applied multivariate statistical analyses to pollen size, number of pores, pollen wall thickness, and size and density of ornamental elements from light microscopy (LM) and Scanning Electronic Microscope (SEM) images. Additionally, random forest classification models were applied to test the accuracy of differentiating Altingiaceae pollen types. Our results reveal significant morphological overlap between the pollen of evergreen Altingia and deciduous Liquidambar, with classification models showing limited accuracy and explainability. Thus, fossil pollen of Altingiaceae cannot be confidently classified into evergreen or deciduous types, highlighting challenges in using their pollen morphology for taxonomic classification in palaeoecological research.

NiMnO nanoparticle-activated carbon anodes for efficient urea oxidation and energy production in wastewater-driven direct urea fuel cells

The growing concern over urea-containing wastewater from industrial sources necessitates innovative treatment solutions that also offer sustainable energy production. In this study, a novel anode material is developed by decorating activated carbon with NiMnO nanoparticles through thermal treatment under an inert atmosphere. The resulting NiMnO NPs-decorated activated carbon was evaluated for its electrocatalytic performance in the electrooxidation of urea and its application in a direct urea fuel cell (DUFC). X-ray diffraction patterns confirmed the formation of nickel metal and Mn(II) oxide, with activated carbon showing representative peaks. Scanning electron microscopy images revealed well-dispersed nanoparticles on the activated carbon surface, corroborated by uniform elemental distribution from mapping results. Electrochemical measurements using cyclic voltammetry demonstrated that the 30 wt% MnAc sample exhibited the highest electrocatalytic activity among the tested samples (0, 5, 10, 20, 30, 40 and 50 wt% MnAc) with a maximum current density of 123 mA/cm2 at 3.0 M urea concentration and an onset potential of −0.02 V versus Ag/AgCl. Linear sweep voltammetry of the assembled DUFC showed promising open circuit potentials of 0.82 V and maximum power densities reaching 4.9 W/m2, achieved using industrial wastewater from the Egyptian Chemical Industries Company (KIMA) in Aswan, Egypt. The results highlight the efficacy of NiMnO NPs-decorated activated carbon in both urea oxidation and electrical energy generation. This study not only provides a viable method for treating urea-rich industrial wastewater but also presents a sustainable approach to energy production. The findings underscore the potential of this material for future applications in DUFCs, offering significant environmental and economic benefits.

Thiamine-modified octamolybdate catalyzes solvent-free stereoselective olefin epoxidation with TBHP

Simple stirring of an acidic aqueous solution (pH=3) containing sodium molybdate and thiamine hydrochloride (VB1) at room temperature resulted in an octamolybdate-containing VB1 (MoB1) material as an efficient and cost-effective epoxidation catalyst using tert‑butyl hydroperoxide (TBHP) under solvent-free condition. The stereospecific stilbene oxidation (>99 %) observed in the presence of MoB1 can be originated from the steric hindrance of some groups on the thiamine molecule and π–π stacking interactions of its pyrimidine and/or thiazole rings with phenyl rings of stilbenes. Further olefins such as cyclooctene, indene, 1-octene, and styrenes are efficiently oxidized using MoB1/TBHP catalytic system. The catalyst is composed of two thiaminium dications (C12H18N4OS)2+ and one Mo8O264– tetraanion based on different characterization techniques and chemical compositional analyses. Field Emission Scanning Electron Microscope (FE-SEM) images shows a sheet-like nanostructure for MoB1 comprising layers with thicknesses ranging from 50 to 500 nm. It exhibits a heterogeneous nature in catalysis evidenced by hot filtration test and ICP-OES analysis. X-ray photoelectron spectroscopy (XPS) indicates minor contributions of Mo in the oxidation states +V and +IV in addition to MoVI attributed to partial electron transfer from VB1 to Mo8O264–. The scavenging experiments support the presence of radical species during catalysis, while, they do not damage the structural integrity of the MoB1 catalyst based on the recycling experiments and FT-IR spectra.

Exploring surface integrity: Experimental investigation into abrasive waterjet deep hole drilling on ss 316L for biomedical applications

Precision drilling of difficult-to-cut materials with exceptional surface integrity is a crucial factor in producing advanced manufactured components in industries like aviation, automotive, defense, electronic, and medical devices. More specifically, deep hole drilling enables precise customization of prostheses, improving patient comfort and functionality. Abrasive waterjet deep hole drilling has become a vital drilling technique in many industries due to its adaptability and effectiveness in drilling intricate shapes on hard-to-cut materials. The interplay between process parameters and surface finish underscores the need for systematic investigation to enhance drilling efficiency and quality. In this research, an attempt has been made to explore the influence of abrasive waterjet deep hole process parameters viz water pressure and standoff distance on the surface integrity of the drilled holes for biomedical applications. A surface roughness tester has been used to evaluate surface roughness at three distinctive places, namely the top, middle, and bottom of the drilled holes. The investigation showed that surface roughness at the top of the holes is less as compared to the middle and bottom of the holes. The average surface roughness along the depth of the drilled holes is greatly influenced by water pressure. Additionally, the morphology of the drilled holes has been studied using a scanning electron microscope (SEM). SEM images revealed that the top surface of the drilled holes is free from defects.

Self‐Assembly of UiO‐66 on Conjugated Polyelectrolytes: Toward Enhanced Photophysical Properties

AbstractIn this study, the synthesis and characterization of the fluorescent metal–organic framework (MOF)‐polymer composites is reported based on zirconium‐based MOFs (UiO‐66 and UiO‐66(OH)₂) and a conjugated polyelectrolyte, poly(phenylene ethynylene) carboxylate (PPE‐CO₂‐108). The defect‐rich nature of these Zr‐MOFs facilitates strong interactions between the polyelectrolyte's carboxylic acid moieties and the open metal sites on the Zr clusters within the MOF nanoparticles. The composites are prepared by a simple impregnation approach, where MOF nanocrystals suspended in HEPES buffer are added to the polymeric solution under sonication for 10 min. The obtained MOF composites (i.e., UiO‐66‐CPE and UiO‐66 (OH)2‐CPE) are characterized using powder X‐ray diffraction (PXRD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), Brunauer‐Emmett‐Teller (BET) surface area, zeta potential measurements, and UV–vis spectroscopy. The characterization confirmed the homogeneous distribution of the MOF nanocrystals on the polymer as seen in the SEM images, and the interaction with PPE‐CO₂‐108 is confirmed by the decrease in the surface areas from 1050 to 590 m2 g−1 for UiO‐66‐CPE and from 500 to 137 m2 g−1, for UiO‐66(OH)2‐CPE. Fluorescence microscopy revealed strong fluorescence in the microparticles, confirming robust polymer‐MOF interaction. The composites also exhibit improved photostability of the conjugated polyelectrolyte, suggesting their potential for applications in biomedical imaging and other areas requiring stable and bright fluorescent systems.

A pH-Responsive Hydrogel for the Oral Delivery of Ursolic Acid: A Pentacyclic Triterpenoid Phytochemical.

In this study, poly(HEMA-PEGxMEM-IA) hydrogels were prepared by radical copolymerization of poly(ethylene glycol) methyl ether methacrylate (PEGxMEM), 2-hydroxyethyl methacrylate (HEMA), and itaconic acid (IA). The reaction was carried out in ethanolic solution using N,N'-methylenebisacrylamide (MBA) as a crosslinking agent and 1-hydroxycyclohexyl phenyl ketone (HCPK) as a photo-initiator. The poly(HEMA-PEGxMEM-IA) hydrogels (HGx) were evaluated as a delivery system for ursolic acid (UA), a phytochemical extracted from the plant Clinopodium revolutum, "flor de arena". The hydrogels were characterized by Fourier-transform infrared spectroscopy (FTIR-ATR), Raman spectroscopy, X-Ray diffraction (XRD), thermogravimetric analysis (TGA), and scanning electron microscopy (SEM). The swelling behavior was studied in buffer solutions from pH 2 to 10, specifically at pH 2.2 (gastric environment) and 7.4 (intestinal environment). It was found that the hydrogels studied showed sensitivity to pH. At pH 2.2, the degree of swelling for HG5 and HG9 hydrogels was 0.45 and 0.93 (g water/g hydrogel), respectively. At pH 7.4, the degree of swelling for HG5 and HG9 hydrogels was 1.97 and 2.64 (g water/g hydrogel), respectively. The SEM images show the variation in pore size as a function of pH, and the UA crystals in the pores of the hydrogels can also be observed. The in vitro UA release data best fit the Korsmeyer-Peppas kinetic model and the diffusion exponent indicates that the release mechanism is governed by Fickian diffusion.

Effects of NaCl/KCl ratios on structural and properties changes in soy‐potato protein mixed gel

SummaryTo reduce the sodium salt content in protein gel‐based foods, this study investigated the effects of different Na‐K ratios on the gelation properties and structural changes of soy protein isolate (SPI) and potato protein isolate (PPI) composite gels. The results showed that the composite gel properties were further enhanced with increasing Na‐K ratio in the SPI/PPI gel system. Specifically, when the Na‐K ratio was 1:1, the SPI/PPI composite gel exhibited the highest gel strength, gel elasticity, WHC, storage modulus (G′), and β‐sheet content, whereas the α‐helix content and β‐turn content were the lowest. Scanning electron microscopy images revealed a dense and uniform network structure of the composite gel. The addition of low concentrations of Na+ and K+ improved the network structure and water‐holding capacity of the SPI/PPI gel during the heat‐induced gelation process. However, excessively high Na‐K ratios weakened the gel properties.

Dynamics of localized accelerated corrosion in reinforced concrete: Voids, corrosion products, and crack formation

A comprehensive 3D imaging analysis was conducted to investigate the corrosion process in reinforced concrete (RC) samples at various stages of the accelerated galvanostatic corrosion process. A state-of-the-art X-ray computed tomography (CT) scan technology was utilized to collect high-resolution 3D images of the specimen. The CT imaging was complemented and validated using a multi-faceted approach utilizing Scanning electron microscopy (SEM) and Raman spectrometry techniques. The distribution and evolution of voids, corrosion products, and cracks were investigated. A localized corrosion was observed that has some similarity to pitted corrosion but not as wide spread along the bar. The micro-scale imaging investigations revealed a gradual increase in the diameter of voids as the time of corrosion increased, especially after 8 days of accelerated corrosion process at which a significant decrease in small-sized voids (≤0.11 mm) accompanied by an increase in other void sizes was observed. At 10 and 12 days of accelerated corrosion process, the volume of larger-sized voids (≥0.35 mm) continued to increase, indicating a rapid corrosion progress and the formation of corrosion-induced cracks. In addition, a thorough X-ray CT analysis allowed us to differentiate between various categories of corrosion products. Notably, iron oxides and iron hydroxides were found to dominate the corrosion products. Understanding the composition and distribution of these corrosion products is essential as they play a significant role in the degradation and deterioration of the concrete structure. The coexistence of iron oxides and iron hydroxides in the region of corrosion products were confirmed using Raman spectroscopy analysis. The CT scan images captured the evolution of cracks at different time intervals, revealing a strong correlation between the initiation of cracks and the presence of corrosion products. Subsequently, during the cracking in the matrix, while the propagation of corrosion products within the matrix contributed to the expansion of cracks. SEM images and elemental analysis confirmed that these cracks were filled with corrosion products.

An experimental study of fracture mechanism and morphology of granite specimens under various dynamic loading rates

Numerous studies have shown that dynamic fracture toughness (DFT) of rock is dependent on loading rate. This paper quantitatively studied the effect of loading rate on DFT from perspective of mesoscopic fracture morphology. First, notched semi-circle bend (NSCB) and short-core-in-compression (SCC) samples of granite were prepared for dynamic mode I and mode II fracture tests. Then, the DFT values of NSCB and SCC specimens at various loading rates were calculated and analyzed. After that, mesoscopic morphologies of failure surfaces of NSCB and SCC specimens under various loading rates were obtained by scanning electron microscope (SEM). The fracture morphology features of specimens were quantitatively characterized by a method combining deep learning and SEM images. The analytical results suggested that as loading rates rose, the increase in the percentage of mesoscopic fracture morphology caused by shear stress (MFM-S) on the fractured surface was the primary reason for the increase of DFT. When dynamic loading varied from 40 to 120 GPa m1/2 s−1, there was a linear relationship between the DFT and the proportion of MFM-S. Additionally, with an increasing loading rate, the proportion of MFM-S on the fracture surface of NSCB specimens varied slightly more, which can explain why the dependence of DFT on loading rate in NSCB specimens was somewhat more obvious than in SCC specimens.

New evidence of syn-eruptive magma-carbonate interaction: the case study of the Pomici di Avellino eruption at Somma-Vesuvius (Italy)

Calcareous lithics are commonly found within the products of some explosive eruptions of Somma-Vesuvius. The pumice fragments from the final phase of the Plinian fallout event of the Pomici di Avellino eruption contain abundant calcareous xenoliths. Previous work on that eruption, including numerical simulations, suggested that the release of CO2 from the entrapment of carbonates may have prolonged the magmatic phase of the eruption by maintaining sufficient driving pressure in the feeding dike. The texture and thermo-metamorphic reactions of carbonate xenolith-bearing pumice fragments of the Pomici di Avellino eruption are analyzed through petrography, scanning electron microscope images, energy dispersive spectrometer analyses, and micro-computed X-ray tomography to deduce the behavior of short-term carbonate-magma interaction and its contribution to the eruption dynamics. Results show that calcareous xenoliths experienced short-term magma-carbonate interaction, which took place in three steps: (i) entrainment, i.e., the mechanical process of carbonate xenoliths entrapment into a magma; (ii) decarbonation, related to high-temperature decomposition reaction of the xenoliths; and (iii) digestion or dissolution of the incorporated calcareous xenoliths into the melt with diffusion of Ca and Mg. The CO2 released during the syn-eruptive decarbonation process thus provided extra volatiles to the rising magma, which may have maintained magma buoyancy longer than expected if only magmatic volatiles were involved in the eruption.

Effect of wheat bran filler particulates nettle fiber reinforced epoxy matrix composite − A novel material for thermal insulation application

This research examines the mechanical and thermal characteristics of composites made from nettle fiber-reinforced wheat bran filler particulate epoxy framework. It highlights the influence of different filler materials on the performance of these composites. A thorough examination of mechanical properties was carried out, focusing on the flexibility, bending strength, impact resistance, and Shore D hardness. The malleable quality was completely changed by adding a filler ingredient, reaching a peak of 51.36 MPa. The flexural strength reached 47.38 MPa, showing excellent ability to withstand loads. The assessment of affect quality reached a maximum of 13 kJ/m2, indicating high energy absorption and durability. The Shore D hardness, which indicates the surface’s ability to resist indentation, ranged from 52 to 61, indicating differences in the stiffness of the composite material. The addition of bran filler to this composite provides an ideal thermal conductivity value of 0.98 W/mK. The morphological properties of the composites were analysed using Scanning Electron Microscopy (SEM), which provided detailed insights into their internal structure. The SEM images revealed a uniform distribution of nettle filaments and bran fillers inside the epoxy matrix, with well-formed samples exhibiting strong fiber–matrix adhesion and minimal voids.