Scanning Electron Microscopy Image Analysis Research Articles

Anodized SLM Ti6Al4V surfaces: influence of surface characteristics on NTs growth and resulted surfaces properties.

TiO2 nanotubes (NTs) obtained via electrochemical anodization (EA) on conventionally machined titanium surfaces are reported to be promising for achieving mucointegration in dental implant therapy. Dental abutments, manufactured by selective laser melting (SLM), combined with thermal post-treatment, present a promising alternative to conventionally machined titanium. Based on an original protocol, this study aims to investigate how the characteristic microstructure of the α + β phases in post-heated SLM Ti6Al4V can influence the growth of NTs and the resulting physical and chemical surface properties. Ti6Al4V-SLM discs were fabricated, heat post-treated and mechanically polished. The samples were then subjected to EA under different voltage conditions (10, 20 and 30 V). The specimens' surfaces were characterized at the same location, before NTs formation by electron backscatter diffraction (EBSD), and after by scanning electron microscopy (SEM). Then, roughness and wettability were studied to determine how EA affects surface properties compared to conventionally machined and polished titanium surfaces without NTs (reference). Surface reactivity was evaluated through chemical analysis and collagen binding capacities. The self-organized TiO2 layer was developed on the α phase only and the β phase was preferentially dissolved. The characteristic dimensions of the nanotubes (diameter, length and wall thickness), measured by SEM image analysis, increased proportionally with the rise in voltage but were not affected by the crystallographic orientation of the underlying α grain. Micro-roughness was the same for nanotubular and reference surfaces. Wettability was improved, as was surface reactivity towards collagen, which may contribute to improved bioactivity of titanium surfaces in dentistry.

Fabrication and characterization of an electrospun silk fibroin/gelatin transparent graft material for corneal epithelial regeneration

The damaged corneal epithelial causing loss of vision can be restored by epithelial tissue regeneration through tissue engineering approach that provides an engineered corneal substitute with appropriate properties and nanofibrous architecture. This works reports a polymeric matrix that was derived from silk fibroin (SF) and gelatin (GE) natural polymer blend with optimized composition resembling the structure and function of the native epithelial tissue. SF/GE blend spinning solutions prepared with different volume ratios of SF/GE: 70/30, 50/50, and 30/70 were used to fabricate electrospun mats. The fabricated two-dimensional mats had nanofibrous porous architecture having interconnected pores with pore size range of 175–267 nm suitable for corneal epithelial regeneration and 891.2–558 nm fiber diameter range as revealed by scanning electron microscopic image analysis. The performed Fourier transform infrared spectra confirmed the presence of individual polymers in the scaffolds and the scaffolds are hydrophilic in nature. Among the scaffolds, SF/GE 70:30 and SF/GE 50:50 composition possess desired porosity range of 87–88%. The tensile strength was slightly decreased with increase in GE content and the strength obtained was in the range 2.74–2.26 Mpa. An enhanced transparency was obtained with increased GE concentration, the transparency range of 73–82% observed with SF/GE:50/50 matches with the transparency of natural corneal epithelium. The biocompatibility of the scaffolds was confirmed by cell attachment, cytotoxicity and ROS evaluation by culturing rabbit corneal fibroblast cells (SIRC) on the scaffolds. Among the scaffolds, SF/GE: 70/30 exhibited the highest cell viability, but with less transparency ranging 55–71%. Therefore, considering all the properties, SF/GE with 50:50 ratio scaffold may be a suitable substrate in the field of corneal tissue engineering.

Impact of spraying commercial Bentonite Nanoclay on fortification of the mortar as Nano Sprying Technique (NST) in heritages and historical buildings

Spraying Bentonite NanoClay as an innovative idea satisfied an urgent need for conservation of historical brick constructions. This research explores the application of Nanotechnology as a Nano-Geotechnics (NaG) and Nano Ground Improvement (NGI) techniques for fortifying the mortar between bricks in historical buildings against some environmental erosive factors. Bentonite Nanoparticles were selected because of their compatibility with mortar. They were applied via Nano Spray to mitigate holes and cracks caused by erosion. Various percentages of bentonite NanoClay (2–10%) Spray and the number of times to spray on the mortar were evaluated. Validation through field emission scanning electron microscopy imaging (FESEM/SEM), X-Ray differaction and Fluorescence analyses (XRD/XRF), Inductively coupled plasma optical emission spectroscopy (ICP-OES), Brunauer–Emmett–Teller (BET), porosity tests, water absorption time measurement, and weathering tests confirmed the efficacy and long-term stability of this method. The result indicated that double spraying of a 2% NanoClay solution proved most effective in reducing porosity, declining water absorption, and enhancing resistance to freezing and rain.

Cobalt-Doped ZnO Nanocomposits for Efficient Dye Degradation: Charge Transfer.

Doping enhances the optical properties of high-band gap zinc oxide nanoparticles (ZnO NPs), essential for their photocatalytic activity. We used the combustion approach to synthesize cobalt-doped ZnO heterostructure (CDZO). By creating a mid-edge level, it was possible to tune the indirect band gap of the ZnO NPs from 3.1 eV to 1.8 eV. The red shift and reduction in the intensity of the photoluminescence (PL) spectra resulted from hindrances in electron-hole recombination and sp-d exchange interactions. These improved optical properties expanded the absorption of solar light and enhanced charge transfer. The field emission scanning electron microscopy (FESEM) image and elemental mapping analysis confirmed the CDZO's porous nature and the dopant's uniform distribution. The porosity, nanoscale size (25-55 nm), and crystallinity of the CDZO were further verified by high-resolution transmission electron microscopy (HRTEM) and selected area electron image analysis. The photocatalytic activity of the CDZO exhibited much greater efficiency (k=0.131 min-1) than that of ZnO NPs (k=0.017 min-1). Therefore, doped heterostructures show great promise for industrial-scale environmental remediation applications.

Compatibility study of recycled Polypropylene (PP)/Poly(ethylene terephthalate) (PET) blends nanocomposites with PP‐g‐MAH: Modeling of twin screw extrusion

AbstractAlthough the utilization of recycled polymers is essential to sustain the environment, conventional recycled polymers face limitations in application due to the degradation of their properties caused by impurities. To solve the problem the performance deterioration of these recycled polymers, this study aimed to enhance their compatibility by chemically adding polypropylene‐graft‐maleic anhydride (PP‐g‐MAH) and physically manipulate a screw profile by using an extrusion simulation program. As a result of applying the optimized extrusion process set by the simulation program, significant improvements in the compatibility and dispersion of fillers within the polymer were observed through scanning electron microscopy image analysis. In addition, through detailed analysis of rheological data, the positive impact of adding compatibilizer and changing screw profile on rheological properties was demonstrated. As the compatibility of recycled polymer blends improved, tensile strength increased by approximately two‐fold and thermal conductivity was significantly improved, which were decisive factors in dramatically enhancing the performance of recycled polymers. These improved polymer properties provide an opportunity for recycled polymers to be applied more broadly and will expand the potential for new applications in various industrial fields.

Assessment of Conductive Sites on Carbon-Fiber Reinforced Polymer

Carbon-fiber reinforced polymer (CFRPs) composites can drive galvanic corrosion of other metals with which they are in contact such as aluminum alloys (AAs) when exposed to aggressive environments. In these galvanic couples, CFRP behaves as a cathode, owing to the noble nature of carbon, whereas the coupled metal behaves as an anode that undergoes accelerated deterioration. To be able to control the corrosion, it is critical to understand the electrochemical activity of CFRP. In this work, a copper deposition technique was developed to quantify the extent of electrochemical activity and identify the exact location of electrochemically active sites on the CFRP. Optimization of the deposition parameters was performed by focused ion beam sectioning and viewing the Cu-deposited cross sections in a scanning electron microscope (SEM). Quantification of the electrochemically active area was done through large-area imaging by SEM and optical microscopy and image analysis. The top surfaces and cross sections of deposit/CFRP interfaces were investigated by viewing at high magnification to evaluate polymer coverage and surface defects.

Determining the orderliness of carbon materials with nanoparticle imaging and explainable machine learning.

Carbon materials have paramount importance in various fields of materials science, from electronic devices to industrial catalysts. The properties of these materials are strongly related to the distribution of defects-irregularities in electron density on their surfaces. Different materials have various distributions and quantities of these defects, which can be imaged using a procedure that involves depositing palladium nanoparticles. The resulting scanning electron microscopy (SEM) images can be characterized by a key descriptor-the ordering of nanoparticle positions. This work presents a highly interpretable machine learning approach for distinguishing between materials with ordered and disordered arrangements of defects marked by nanoparticle attachment. The influence of the degree of ordering was experimentally evaluated on the example of catalysis via chemical reactions involving carbon-carbon bond formation. This represents an important step toward automated analysis of SEM images in materials science.

Melt electrowriting of poly(ϵ-caprolactone)—poly(ethylene glycol) backbone polymer blend scaffolds with improved hydrophilicity and functionality

Melt electrowriting (MEW) is an additive manufacturing technique that harnesses electro-hydrodynamic phenomena to produce 3D-printed fibres with diameters on the scale of 10s of microns. The ability to print at this small scale provides opportunities to create structures with incredibly fine resolution and highly defined morphology. The current gold standard material for MEW is poly(ϵ-caprolactone) (PCL), a polymer with excellent biocompatibility but lacking in chemical groups that can allow intrinsic additional functionality. To provide this functionality while maintaining PCL’s positive attributes, blending was performed with a Poly(Ethylene Glycol) (PEG)-based Acrylate endcapped Urethane-based Precursor (AUP). AUPs are a group of polymers, built on a backbone of existing polymers, which introduce additional functionality by the addition of one or more acrylate groups that terminate the polymer chain of a backbone polymer. By blending with a 20kDa AUP-PEG in small amounts, it is shown that MEW attributes are preserved, producing high-quality meshes. Blends were produced in various PCL:AUP weight ratios (100:0, 90:10 and 0:100) and processed into both solvent-cast films and MEW meshes that were used to characterise the properties of the blends. It was found that the addition of AUP-PEG to PCL significantly increases the hydrophilicity of structures produced with these polymers, and adds swelling capability compared to the non-swelling PCL. The developed blend (90:10) is shown to be processable using MEW, and the quality of manufactured scaffolds is evaluated against pure PCL scaffolds by performing scanning electron microscopy image analysis, with the quality of the novel MEW blend scaffolds showing comparable quality to that of pure PCL. The presence of the functionalisable AUP material on the surface of the developed scaffolds is also confirmed using fluorescence labelling of the acrylate groups. Biocompatibility of the MEW-processable blend was confirmed through a cell viability study, which found a high degree of cytocompatibility.

Investigating correlations between microstructural characteristics and mechanical properties of coral sand mortar with different silica fume contents

The use of coral sand in concrete and mortar for ocean engineering has led to significant reductions in construction costs and improved construction efficiency. However, this approach poses challenges such as low strength, high brittleness, and high porosity. To address these challenges, this study incorporated silica fume to enhance the mechanical properties of the mortar and investigated the effects of different silica fume contents on the hydration process, pore structure, and strength of coral sand mortar. Additionally, this study introduced a novel iterative approach combining low-field nuclear magnetic resonance and scanning electron microscopy image analysis to determine transverse relaxivity (ρ2). During the early hydration process, the intensity spectrum of coral mortar exhibited three peaks at 298, 1841, and 299 au, corresponding to transverse relaxation times (T2) of 0.64, 6.83, and 83.10 ms, respectively. Over a 6 h hydration period, the spectrum of the specimen prepared with white cement exhibited an additional peak that gradually merged with the main peak. As the curing period extended from 7 to 28 days, the porosity of coral sand mortar decreased by 3.77–4.55 %, while the strength increased by 7.43–14.35 MPa across silica fume contents ranging from 6 % to 24 %. With increasing silica fume content, the calcium–silicon ratio of the samples gradually decreased, promoting the formation of more floccus C–S–H gels. Consequently, the sample porosity first decreased slightly. After 28 days of curing, the coral sand mortar containing 12 % silica fume exhibited the highest strength owing to the increased amount of floccus C–S–H gels. These gels gradually filled the pores between the fibrous C–S–H gels, forming a compact spatial reticular structure. This structure mitigated the adverse impact of high porosity on mortar strength.

Chain-like One-Dimensional Assembly of Mesoporous Silica Nanoparticles: An Approach To Improve Hydrogel Adhesion.

Mesoporous silica nanoparticles (MSNPs) are well known for their adhesive properties with hydrogels and living tissues. However, achieving direct contact between the silica nanoparticle surface and the adherend necessitates the removal of capping agents, which can lead to severe aggregation when exposed to wet surfaces. This aggregation is ineffective for simultaneously bridging the two adherends, resulting in a reduced adhesive strength. In this study, we designed and synthesized mesoporous silica nanochains (MSNCs) to enhance the interactions with hydrogels by promoting the formation of coarser structures with increased nanopore exposure. Chain-like one-dimensional assemblies in the MSNCs were generated by depleting the capping ligand, cetyltrimethylammonium bromide, from the surface of the MSNPs. To quantify the porous areas of the MSNCs, we analyzed scanning electron microscopy (SEM) images using an in-house SEM image analysis algorithm. Additionally, we conducted a comparative assessment of the adhesion energies of MSNCs and MSNPs on a poly(dimethylacrylamide) hydrogel using a universal testing machine. The MSNCs exhibited a maximum adhesion energy of 13.7 ± 0.7 J/m2 at 3 wt %, surpassing that of MSNPs (10.9 ± 0.3 J/m2) at 2 wt %. Moreover, the unique stacking structure of the MSNCs enabled them to maintain an adhesion energy of 13.4 ± 1.0 J/m2 at a high concentration of 9 wt %, whereas the adhesion energy of MSNPs decreased to 8.2 ± 0.4 J/m2. This underscores their potential as superior hydrogel adhesives in challenging wet tissue-like environments.

Comparison of morphology, protein concentration, and size distribution of bone marrow and Wharton's jelly-derived mesenchymal stem cells exosomes isolated by ultracentrifugation and polymer-based precipitation techniques

Exosomes which are tiny extracellular vesicles (30–150 nm), transport vital proteins and gene materials such as miRNA, mRNA, or DNA, whose role in cell communication and epithelia regulation is critical. Many techniques have been developed as a result of studying exosomes' biochemical and physicochemical properties, although there is still no standard method to isolate exosomes simply with high yield. Commercial kits have gained popularity for exosome extraction despite concerns about their effectiveness in scientific research. On the other hand, ultracentrifugation remains the gold standard isolation method. This study compares these two common exosome isolation methods to determine their impact on the quality and quantity of exosomes isolated from bone marrow (BM) and Wharton's jelly (WJ)-derived mesenchymal stem cells. Isolated exosomes from the two sources of the cell's conditioned medium by two methods (polymer kit and ultracentrifuge) were characterized using western blotting, scanning electron microscopy (SEM), dynamic light scattering (DLS), and the Bradford assay. Western blot analysis confirmed separation efficiency based on CD81 and CD63 markers, with the absence of calnexin serving as a negative control. The Morphology of exosomes studied by SEM image analysis revealed a similar round shape appearance and their sizes (30–150 nm) were the same in both isolation techniques. The DLS analysis of the sample results was consistent with the SEM ones, showing a similar size range and very low disparity. The exosome protein content concentration analysis revealed that exosomes isolated by the polymer-based kits contained higher protein concentration density and purity (p <0.001). In general, though the protein yield was higher when the polymer-based kits were used, there were no significant differences in morphology, or size between WJ-derived and BM-derived exosomes, regardless of the isolation method employed.

Thermomechanical and physicochemical evolution of meat‐analogue based fried foods

SummaryThis study aimed to get mechanistic insights on the evolution of major quality attributes of meat‐analogue (MA) based batter‐coated fried products. Wheat and rice flour‐based batter systems were used to coat a MA. The products were deep‐fried at 180°C for 4 min in canola oil and their post‐fry quality changes at room environment (RE, 25°C) and under IR‐heating (65 °C) were investigated. Results showed that in addition to moisture‐fat profile, batter coating substantially (P &lt; 0.05) influenced the development of thermal, textural, colour and microstructural traits of MA. Post‐fry colour changes (ΔE value: 3.1 to 10.4) in MA‐based coated product continued under IR‐heating (65 °C). Evolution of the thermal, textural and colour attributes of MA‐based coated products were significantly (P &lt; 0.05) influenced by the formulation of outer batter coatings. Moisture migration occurred from high moisture (ranged from 1.07 to 1.25 g g−1 dry matter) containing core to dry (moisture ranged from 0.15 to 0.59 g g−1 dry matter) crust region of MA‐based coated fried product, where the moisture migration was interlaced with batter formulations. Holding environment and duration substantially (P &lt; 0.05) impacted the textural properties (hardness, brittleness and crispiness) of MA‐based coated fried product. Glass transition temperature (Tg) of coated fried products were ranged between −20.4 to −23.0 °C, that explains quality changes at RE and under IR‐heating. Scanning electron microscopic image analysis (surface openings: 5.7 to 27.31%; fractal dimension: 2.555 to 2.702) revealed the impact of surface microstructure and mass‐transfer modulated textural development in MA‐based coated products. FTIR spectroscopy revealed surface chemical profile in relation to colour evolution of MA‐based fried products. Principal component analysis outcome (PC1: 52.9.% and PC2: 25.8%) revealed varying extent of correlation between studied thermomechanical and physicochemical attributes.

Performance of solid-oxide fuel cells operating with different sustainable fuel reformates

Solid oxide fuel cells (SOFCs) are recognized for their outstanding fuel flexibility and high efficiency in converting chemical energy into electrical energy. This research presents experiments on SOFCs fed with humidified hydrogen and hydrogen-rich gaseous reformates derived from methanol and ammonia: methanol steam reforming (MSR), methanol decomposition (MD), and ammonia decomposition (AD), at 700–850 °C. Results of SOFCs operating with MD reformate on different types of SOFCs, which to the best of our knowledge aren't available in the literature, are presented and compared with other reformate types for the first time. MD-reformate yielded the highest cell performance, with the least disparity in power density from humidified hydrogen, followed by AD-, and MSR-reformates. The study compares the direct internal reforming method, and the innovative Combined Electro-Thermo-Chemical cycle's potential. Introducing the concept of critical power density, the research evaluates fuel utilization across SOFC types. Scanning Electron Microscopy imaging and Energy-Dispersive X-ray Spectroscopy analyses confirm the viability of CO as a fuel, with no carbon deposits on the anodes when using MD-reformate. The findings demonstrate the suitability of using methanol- and ammonia-decomposition products in SOFCs and their compatibility with hybrid power generation cycles.

High‐Performance NiCo2O4/Graphene Quantum Dots for Asymmetric and Symmetric Supercapacitors with Enhanced Energy Efficiency

AbstractFor the sustainable growth of future generations, energy storage technologies like supercapacitors and batteries are becoming more and more common. However, reliable and high‐performance materials’ design and development is the key for the widespread adoption of batteries and supercapacitors. Quantum dots with fascinating and unusual properties are expected to revolutionize future technologies. However, while the recent discovery of quantum dots honored with a Nobel prize in Chemistry, their benefits for the tenacious problem of energy are not realized yet. In this context, herein, chemical‐composition tuning enabled exceptional performance of NiCo2O4(NCO)/graphene quantum dots (GQDs) is reported, which outperform the existing similar materials, in supercapacitors. A comprehensive study is performed on the synthesis, characterization, and electrochemical performance evaluation of highly functional NCO/GQDs in supercapacitors delivering enhanced energy efficiency. The high‐performance, functional NCO/GQDs electrode materials are synthesized by the incorporation of GQDs into NCO. The effect of variable amount of GQDs on the energy performance characteristics of NCO/GQDs in supercapacitors is studied systematically. In‐depth structural and chemical bonding analyses using X‐ray diffraction (XRD) and Raman spectroscopic studies indicate that all the NCO/GQDs composites crystallize in the spinel cubic phase of NiCo2O4 while graphene integration evident in all the NCO/GQDs. The scanning electron microscopy imaging analysis reveals homogeneously distributed spherical particles with a size distribution of 5–9 nm validating the formation of QDs. The high‐resolution transmission electron microscopy analyses reveal that the NCOQDs are anchored on graphene sheets, which provide a high surface area of 42.27 m2g−1 and high mesoporosity for the composition of NCO/GQDs‐10%. In addition to establishing reliable electrical connection to graphene sheets, the NCOQDs provide reliable 3D‐conductive channels for rapid transport throughout the electrode as well as synergistic effects. Chemical‐composition tuning, and optimization yields NCO/GQDs‐10% to deliver the best specific capacitance of 3940 Fg−1 at 0.5 Ag−1, where the electrodes retain ≈98% capacitance after 5000 cycles. The NCO/GQD‐10%//AC asymmetric supercapacitor device demonstrates outstanding energy density and power density values of 118.04 Wh kg−1 and 798.76 W kg−1, respectively. The NCO/GQDs‐10%//NCO/GQDs‐10% symmetric supercapacitor device delivers excellent energy and power density of 24.30 Wh kg−1 and 500 W kg−1, respectively. These results demonstrate and conclude that NCO/GQDs are exceptional and prospective candidates for developing next‐generation high‐performance and sustainable energy storage devices.

SEM Image Processing Assisted by Deep Learning to Quantify Mesoporous γ-Alumina Spatial Heterogeneity and Its Predicted Impact on Mass Transfer.

The pore network architecture of porous heterogeneous catalyst supports has a significant effect on the kinetics of mass transfer occurring within them. Therefore, characterizing and understanding structure-transport relationships is essential to guide new designs of heterogeneous catalysts with higher activity and selectivity and superior resistance to deactivation. This study combines classical characterization via N2 adsorption and desorption and mercury porosimetry with advanced scanning electron microscopy (SEM) imaging and processing approaches to quantify the spatial heterogeneity of γ-alumina (γ-Al2O3), a catalyst support of great industrial relevance. Based on this, a model is proposed for the spatial organization of γ-Al2O3, containing alumina inclusions of different porosities with respect to the alumina matrix. Using original, advanced SEM image analysis techniques, including deep learning semantic segmentation and porosity measurement under gray-level calibration, the inclusion volume fraction and interphase porosity difference were identified and quantified as the key parameters that served as input for effective tortuosity factor predictions using effective medium theory (EMT)-based models. For the studied aluminas, spatial porosity heterogeneity impact on the effective tortuosity factor was found to be negligible, yet it was proven to become significant for an inclusion content of at least 30% and an interphase porosity difference of over 20%. The proposed methodology based on machine-learning-supported image analysis, in conjunction with other analytical techniques, is a general platform that should have a broader impact on porous materials characterization.

Optimization of Ion Beam-Assisted Deposition Process for Y&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; Film to Enhance Plasma Resistance

A ceramic-based plasma etcher window (Lid) requires robust resistance to plasma, especially when exposed to harsh fluorine-based plasma conditions. In this study, a Y&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;4&lt;/sub&gt; film was deposited using e-beam evaporation with ion beam-assisted deposition (IBAD), and the physical properties of the IBAD-based Y&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;4&lt;/sub&gt; coating film were thoroughly examined to enhance the mechanical and chemical resistance of the ceramic part, including the Y&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;4&lt;/sub&gt; film, against etching plasma. The hardness and surface morphology of the IBADbased Y&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;4&lt;/sub&gt; could be precisely controlled by various deposition processing parameters, such as beam voltage, beam current, and Ar/O2 gas ratio. Following the IBAD deposition of the Y&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;4&lt;/sub&gt; film, a plasma etching process (Ar/CF&lt;sub&gt;4&lt;/sub&gt; mixture gases with 150 W RF power for 60 minutes) was applied to evaluate the plasma resistance of the deposited Y&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;4&lt;/sub&gt; coating film. The surface morphology characteristics of the Y&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;4&lt;/sub&gt; films were compared using atomic force microscopy, and their grain size was studied through scanning electron microscopy image analysis. Furthermore, a nanoindenter was used to determine the hardness of the Y&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;4&lt;/sub&gt; film. These results suggest that optimizing the IBAD coating process requires an in-depth study that fully considers the correlation between deposition processing parameters and physical properties. This optimization can be instrumental for enhancing the durability of the ceramic part.

Characterisation of bond between cement paste and steel fibres with different surface roughness using SEM.

The performance of cementitious composites reinforced with fibres or/and bars depends on the bond strength between inclusion and cementitious matrix. The nature of formation of fibre-matrix bond is crucial for enhancing the reliability and utilisation of reinforced composites. The research provides a review on the recently published result about the changes in the microstructure of cement matrix surrounding steel fibres with different surface roughness, using a scanning electron microscope (SEM) coupled with k-means clustering algorithm for image segmentation. The debonding pattern of the fibre-matrix bond after the tensile loading cycles was discussed by observing the amount of adhered cement paste to the pulled out fibre surface with SEM. Therefore, analysis of SEM images enabled to explain the connection between the micro-scale properties of cement paste and fibre after application of cyclic loading.

Enhanced dielectric, ferroelectric and piezoelectric properties of lead-free (Ba,Ca)(Sn,Ti)O3 ceramics by optimisation of sintering temperature

Lead-zirconate-titanate [Pb(Zr,Ti)O3 PZT] crystals possess superior ferroelectric, dielectric and piezoelectric properties. However, due to the toxicity of lead there is a demand for lead-free alternatives. In the present work, we focus on the production of the lead-free (Ba,Ca)(Sn,Ti)O3 (BCST) ceramics via solid-state synthesis method. BCST ceramics calcined at 1050°C, 1100°C, 1150°C, 1200°C and 1250°C were characterized using XRD analysis which showed that at temperatures above 1150°C the structure was free from impurities. Rietveld refinements confirmed a tetragonal structure with P4mm space group for the material calcined at 1150°C. Scanning electron microscopy image analysis of samples sintered at 1200°C, 1250°C and 1300°C showed an increase in grain size and density with temperature. The material sintered at 1300°C had a higher dielectric constant compared to other ceramics. A larger grain size facilitated high ferroelectric polarisation (3.38 μC/cm2), dielectric constant (6100) and d33 piezoelectric coefficient (236 pC/N) for the ceramics. This study demonstrates the potential for using lead-free BCST ceramics for device applications, such as piezoelectric actuators, transducers and ultrasonic motors.

Jute Fiber Reinforced Biocomposite: Towards Developing Composite Bone Plate

Bone fractures are often treated with metallic bone plates which are inherited some fundamental issues such as stress shielding, bone atrophy, heavyweight, corrosion, and so on. This work aims to develop a jute epoxy composite to investigate its feasibility to use as a composite bone plate. In this work, the natural fiber-based composite made of jute extracted from the jute plant and epoxy resin obtained from LAPOX® METALAM - B is studied experimentally. The mechanical properties such as tensile, compressive, and bending strength of jute/epoxy composite were measured using the universal testing machine (UTM). Moisture absorption test and scanning electron microscope (SEM) image analysis were also performed. The preliminary results suggest that the jute/epoxy composite could be a potential material for a composite bone plate. However, further detailed studies are required to confirm its applicability as a composite bone plate.

Effects of Multi-Walled Carbon Nanotubes and Recycled Fine Aggregates on the Multi-Generational Cycle Properties of Reactive Powder Concrete

In order to investigate the effect of multi-walled carbon nanotubes (MWCNTs) on the recyclable properties of multi-generation recycled concrete, the physical properties of multi-generation recycled fine aggregate and the mechanical properties of multi-generation recycled concrete with different dosages of MWCNTs were tested, and the enhancement mechanism was analyzed by scanning electron microscopy (SEM). The results showed that the apparent density of multi-generation recycled fine aggregate with 0.05 wt% MWCNTs was increased by 1.04~2.03%, the crushing value was decreased by 38.21~49.45%, the compressive strength of the concrete prepared by it was increased by 11.11~18.96%, the splitting tensile strength was increased by 10~43.94%, the flexural strength was increased by 13.62~22.23%, and the mechanical properties were analyzed by scanning electron microscopy (SEM). Combined with the scanning electron microscope image analysis, the MWCNTs can fill the pores inside the specimen, bridge the cracks, and retard the decrease in concrete strength after multi-generation recycling.