Environmental Scanning Electron Microscopy Research Articles

Integrating continuous mineral-impregnated carbon fibers into digital fabrication with concrete

Digital concrete technologies, such as 3D concrete printing, have the potential to be game changers in the construction industry by reducing material consumption and offering a high level of automation. This not only provides a solution to the shortage of qualified workers but also makes construction sites more attractive workplaces. However, a significant challenge lies in integrating reinforcement, as traditional methods quickly reach their limits, particularly in geometrically complex, material-minimized structures. A potential solution is the use of mineral-impregnated carbon fibers (MCF) reinforcement, which offers high flexibility for 3D printing and better bonding to concrete compared to polymer coating, among other advantages. This article presents the integration of both freshly impregnated and cured MCF into two different concretes in the context of digital fabrication: 3D-printed concrete (3DPC) and self-compacting concrete (SCC). A particular focus was on the mechanical performance of MCF and MCF-reinforced concrete, as well as on the bond behavior between MCF and concrete. The second focus was on the production method. Therefore, samples were conventionally cast with SCC, while layered pouring or printing were used for producing specimens with 3DPC. It was found that the cured MCF exhibited a notably better bond, enhanced by 50%, to both 3DPC and SCC compared to freshly impregnated yarns. Subsequently, when subjected to uniaxial tensile loading, a significantly higher crack density and more uniform crack distribution could be observed in composites with cured MCF using digital image correlation (DIC). This effect was particularly pronounced in printed specimens and confirmed with computed tomography (CT) and environmental scanning electron microscope (ESEM) images.

Antimicrobial effects of catnip (Nepeta cataria L.) essential oil against canine skin infection pathogens

Background and Aim: Catnip essential oils have antimicrobial effects against bacteria, yeast, and fungi; however, there is limited information regarding their antimicrobial activity against pathogens that cause canine skin infections. This study aimed to identify the phytochemical constituents of catnip essential oil and assay its antimicrobial activity against Staphylococcus pseudintermedius, Malassezia pachydermatis, Microsporum canis, Microsporum gypseum, Microsporum gallinae, and Trichophyton mentagrophytes. Materials and Methods: Catnip essential oil was extracted by hydrodistillation, and its chemical constituents were analyzed by gas chromatography–mass spectrometry (GC–MS). In vitro antimicrobial activity was investigated using broth microdilution and time-kill tests. To evaluate the effect of catnip essential oil on microbial morphology and cell membrane integrity, scanning electron microscopy (SEM) and leakage studies were conducted. Results: GC–MS analysis revealed that the principal components of catnip essential oil were cis- and trans-nepetalactone (57.09% of peak area), trans-, cis-nepetalactone (39.69% of peak area), trans-caryophyllene (1.88% of peak area), and caryophyllene oxide (1.34% of peak area). The minimum inhibitory concentration, minimum bactericidal concentration, and minimum fungicidal concentration values determined by broth microdilution ranged from 0.0625 mg/mL to 4.0 mg/ mL. Time-kill testing showed that the germicidal effects of catnip essential oil were time and concentration-dependent, respectively. Environmental SEM and cell leakage analysis indicated that catnip essential oil disrupted the integrity of cell membranes in the tested microorganisms. Conclusion: Catnip essential oil has potential as an alternative antimicrobial against a wide range of canine skin infection pathogens, including S. pseudintermedius, M. pachydermatis, Mi. canis, Mi. gypseum, Mi. gallinae, and T. mentagrophytes. Keywords: antimicrobial activity, canine dermatitis, catnip, Nepeta cataria.

DEFLECTION AND STRAINS PERFORMANCE OF KENAF FIBRE-REINFORCED CONCRETE BEAMS

There has been a need to find a lasting means to improve beams' deflection and strain performance without necessarily increasing the beam stirrups. The limitations of steel and other synthetic fibres have reduced their application. Given its tensile strength, renewability, sustainability, and affordability compared to steel and synthetic fibres, kenaf fibre development is of great interest in Malaysia. Therefore, this research work experimentally investigated the deflection and strain performance of Kenaf Fibre Reinforced concrete beams. The volume and length of kenaf fibre used were 0.75% and 25mm, respectively. Kenaf fibre was treated with 5% NaOH to improve its performance. The alkaline-treated and untreated kenaf fibres morphology was observed under a variable-pressure scanning electron microscope. It was discovered inclusion of kenaf fibre reduced the workability of concrete. Also, plain and KFR concrete morphology was observed under a variable-pressure scanning electron microscope. Four beams were designed to study the deflection and strain performance of the KFR concrete beam; one was well reinforced but without kenaf fibre. The stirrups spacings were increased by 25%, 50%, and 75% for the other three beams. The beams were tested under centre loading. Deflection and concrete strain at the centre and along the beam span were measured using LVDTs and concrete strain gauges for the four beams. Furthermore, the strains on the shear and bottom flexural reinforcements at the centre of the beam were measured using steel strain gauges. It was discovered that kenaf fibre enhanced the deflection and strain performance of beams between 25% and 50% stirrups deficiency.

Enhanced Strontium Removal through Microbially Induced Carbonate Precipitation by Indigenous Ureolytic Bacteria.

Microbial ureolysis offers the potential to remove metals including Sr2+ as carbonate minerals via the generation of alkalinity coupled to NH4+ and HCO3- production. Here, we investigated the potential for bacteria, indigenous to sediments representative of the U.K. Sellafield nuclear site where 90Sr is present as a groundwater contaminant, to utilize urea in order to target Sr2+-associated (Ca)CO3 formation in sediment microcosm studies. Strontium removal was enhanced in most sediments in the presence of urea only, coinciding with a significant pH increase. Adding the biostimulation agents acetate/lactate, Fe(III), and yeast extract to further enhance microbial metabolism, including ureolysis, enhanced ureolysis and increased Sr and Ca removal. Environmental scanning electron microscopy analyses suggested that coprecipitation of Ca and Sr occurred, with evidence of Sr associated with calcium carbonate polymorphs. Sr K-edge X-ray absorption spectroscopy analysis was conducted on authentic Sellafield sediments stimulated with Fe(III) and quarry outcrop sediments amended with yeast extract. Spectra from the treated Sellafield and quarry sediments showed Sr2+ local coordination environments indicative of incorporation into calcite and vaterite crystal structures, respectively. 16S rRNA gene analysis identified ureolytic bacteria of the genus Sporosarcina in these incubations, suggesting they have a key role in enhancing strontium removal. The onset of ureolysis also appeared to enhance the microbial reduction of Fe(III), potentially via a tight coupling between Fe(III) and NH4+ as an electron donor for metal reduction. This suggests ureolysis may support the immobilization of 90Sr via coprecipitation with insoluble calcium carbonate and cofacilitate reductive precipitation of certain redox active radionuclides, e.g., uranium.

Asbestos Bodies in Human Lung: Localization of Iron and Carbon in the Coating

Asbestos is a term that includes six fibrous mineral phases related to different lung diseases, including asbestosis, lung cancer, and Malignant Pleural Mesothelioma (MPM). Since the last century, these minerals have been widely studied under their mineralogical/chemical and physical aspects with in vivo and in vitro studies to understand the mechanisms of their carcinogenicity. There are several techniques described in the literature, as optical and electron microscopies, for the identification of coated (asbestos bodies, ABs) and uncoated fibers, but only micro-Raman spectroscopy permits a sure characterization of these minerals—and of the related phases—directly in the histological sections of pulmonary parenchyma without any manipulation. In this case, the risk of the loss of associated inorganic phases from asbestos bodies (ABs) and fibers (e.g.: iron or carbonaceous micro-particles) is avoided. Asbestos bodies are produced by the activity of alveolar macrophages with degradation/inactivation of asbestos fibers. Inside the alveolar macrophages, organic and inorganic material settles on the foreign fibers forming an iron-rich proteic and carbonaceous coating. In this study, Variable Pressure Scanning Electron Microscopy with annexed Electron Dispersive Spectroscopy (VP-SEM/EDS) and micro-Raman spectroscopy were applied to the characterization of the phases in the ABs. Characterization of carbonaceous materials (CMs), observed in pristine asbestos phases in previous works, was therefore performed, addressing the micro-Raman laser beam on different points of the asbestos bodies, and Raman mappings on ABs were carried out for the first time. Coupling the data obtained by VP-SEM/EDS and micro-Raman spectroscopy, it was possible to collect information about the iron and carbonaceous phases adhered to the fibers, probably lost during the classical tissue digestion procedures. Information about both mineral and carbonaceous components might be useful to understand the whole structure of “asbestos bodies” and the inflammogenic and carcinogenic effects of the asbestos phases coupled to CMs, that might derive from cigarette smoke or from environmental pollution; this study might be useful to deepen also the possible detrimental role of ABs in the tissues.

Effect of CaCl2 on the micromorphology of a self-thickening agent (TZXJ) for acidizing diversion

The effect of CaCl2 on the micromorphology of a self-thickening agent (TZXJ) was investigated. This study involved analyzing the compositional changes in acid solutions during acid–rock reactions. It combined dynamic light scattering and viscosity testing to confirm that the presence of CaCl2 enhances the aggregation strength of the TZXJ network structure in acid solutions. This enhancement is macroscopically evident as an increase in viscosity. Incorporating 10 % CaCl2 as a promoter into a fresh acid solution, the hydrodynamic radius (Rh) distribution of TZXJ in varying reaction stages was analyzed using dynamic light scattering experiments. The results indicated that the promoter CaCl2 further strengthens the network association of the TZXJ acid solution, thereby improving its thickening capability. Investigating the viscosity of TZXJ aqueous solutions with varying concentrations of CaCl2 revealed that TZXJ exhibits notable salt-thickening effects and can withstand saturated CaCl2 solutions. The microstructural aggregation state and morphology of TZXJ in aqueous solutions were characterized at different CaCl2 concentrations. Dynamic light scattering results demonstrated an increase in the Rh of TZXJ solutions with CaCl2 concentrations. In particular, the mean Rh of a 0.8 % TZXJ solution increased from 150.8 nm to 3078.93 nm. Ultraviolet spectral analysis confirmed that the absorption intensity of the TZXJ solutions increased with CaCl2 concentration, indicating a strengthened network aggregate structure in the TZXJ solutions. Microscopic observations using environmental scanning electron microscopy and transmission electron microscopy revealed that under the influence of calcium chloride, the microstructure of TZXJ transitions from a non-associated, linear carbon chain skeleton to a dense, aggregated network structure. The findings of this study offer theoretical insights for researching polymers resistant to extreme concentrations of CaCl2.

A High-Performance Cr2O3/CaCO3 Nanocomposite Catalyst for Rapid Hydrogen Generation from NaBH4.

This study aims to prepare new nanocomposites consisting of Cr2O3/CaCO3 as a catalyst for improved hydrogen production from NaBH4 methanolysis. The new nanocomposite possesses nanoparticles with the compositional formula Cr2-xCaxO3 (x = 0, 0.3, and 0.6). These samples were prepared using the sol-gel method, which comprises gelatin fuel. The structure of the new composites was studied using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, environmental scanning electron microscopy (ESEM), and X-ray spectroscopy (XPS). The XRD data showed the rhombohedral crystallinity of the studied samples, and the average crystal size was 25 nm. The FTIR measurements represented the absorption bands of Cr2O3 and CaO. The ESEM micrographs of the Cr2O3 showed the spherical shape of the Cr2O3 nanoparticles. The XPS measurements proved the desired oxidation states of the Cr2-xCaxO3 nanoparticles. The optical band gap of Cr2O3 is 3.0 eV, and calcium doping causes a reduction to 2.5 and 1.3 eV at 15.0 and 30.0% doping ratios. The methanolysis of NaBH4 involved accelerated H2 production when using Cr2-xCaxO3 as a catalyst. Furthermore, the Cr1.7Ca0.3O3 catalyst had the highest hydrogen generation rate, with a value of 12,750 mL/g/min.

Mechanical Properties and Microstructure of Highly Flowable Geopolymer Composites with Low-Content Polyvinyl Alcohol Fiber

Geopolymer enhances mechanical properties with polyvinyl alcohol (PVA) fibers, but there has been limited research exploring low PVA fiber dosages for mechanical properties in 3D printing or shotcrete. This study experimentally investigated slag and fly ash-based geopolymer mixtures reinforced with 0.1%, 0.15%, and 0.2% PVA fiber by volume as well as a control group without PVA fibers. These mixtures were prepared using fly ash, quartz sand, slag powder, silica fume, and an aqueous sodium silicate solution as the alkali activator, with the addition of PVA fiber to enhance composite toughness. The mechanical properties of the composites, encompassing dog-bone tensile properties, cubic compressive strength, bending and post-bending compressive strength, and prism compressive properties, were evaluated. Significantly, specimens with 0.15% PVA fibers exhibited optimal performance, revealing a notable 28.57% increase in tensile stress, a 36.45% surge in prism compressive strain, and a 47.59% rise in tensile strain compared to fiber-free specimens. Furthermore, environmental scanning electron microscopy observations were employed to scrutinize the microscopic mechanisms of composites incorporating PVA fibers, slag, and fly ash. In comparison to fiber-free specimens, prism compressive specimens with 0.15% PVA fibers demonstrated a 27.17% increase in post-cracking loading capacity, a 44.07% increase in post-cracking ductility, a 50.00% increase in peak strain energy, and a 76.36% increase in strain energy ratio.

Comparative Study of Exsolved and Impregnated Ni Nanoparticles Supported on Nanoporous Perovskites for Low-Temperature CO Oxidation.

This study investigated the redox exsolution of Ni nanoparticles from a nanoporous La0.52Sr0.28Ti0.94Ni0.06O3 perovskite. The characteristics of exsolved Ni nanoparticles including their size, population, and surface concentration were deeply analyzed by environmental scanning electron microscopy (ESEM), transmission electron microscopy-energy dispersive X-ray spectroscopy (TEM-EDX) mapping, and hydrogen temperature-programmed reduction (H2-TPR). Ni exsolution was triggered in hydrogen as early as 400 °C, with the highest catalytic activity for low-temperature CO oxidation achieved after a reduction step at 500 °C, despite only a 10% fraction of Ni exsolved. The activity and stability of exsolved nanoparticles were compared with their impregnated counterparts on a perovskite material with a similar chemical composition (La0.65Sr0.35TiO3) and a comparable specific surface area and Ni loading. After an aging step at 800 °C, the catalytic activity of exsolved Ni nanoparticles at 300 °C was found to be 10 times higher than that of impregnated ones, emphasizing the thermal stability of Ni nanoparticles prepared by redox exsolution.

Development of Curcumin and Turmerone Loaded Solid Lipid Nanoparticle for Topical Delivery: Optimization, Characterization and Skin Irritation Evaluation with 3D Tissue Model.

Curcuma longa L., commonly known as turmeric, is renowned for its therapeutic benefits attributed to bioactive compounds, namely curcumin (Cur) and aromatic turmerone (Tur), present in its rhizome. These compounds exhibit diverse therapeutic properties, including anti-inflammatory, antioxidant, and anti-tumor effects. However, the topical application of these compounds has a significant potential for inducing skin irritation. This study focuses on formulating solid lipid nanoparticle (SLN) carriers encapsulating both Cur and Tur for reduced irritation and enhanced stability. SLN formulations were prepared by a method using homogenization followed by ultrasonication procedures and optimized by applying response surface methodology (RSM). The optimized SLN formulation demonstrated entrapment efficiencies, with 77.21 ± 4.28% for Cur and 75.12 ± 2.51% for Tur. A size distribution of 292.11 ± 9.43 nm was obtained, which was confirmed to be a spherical and uniform shape via environmental scanning electron microscopy (ESEM) images. The in vitro release study indicated cumulative releases of 71.32 ± 3.73% for Cur and 67.23 ± 1.64% for Tur after 24 hours under sink conditions. Physical stability tests confirmed the stability of formulation, allowing storage at 4°C for a minimum of 60 days. Notably, in vitro skin irritation studies, utilizing the reconstructed human epidermal model (EPI-200-SIT), revealed a significant reduction in irritation with the SLN containing Cur and Tur compared to nonencapsulated Cur and Tur. These findings collectively endorse the optimized SLN formulation as a favorable delivery system for Cur and Tur in diverse topical uses, offering enhanced stability, controlled release and reduced irritation.

Electron Beam-Modified Collagen Type I Fibers: Synthesis and Characterization of Mechanical Response.

Ten MeV electron beam treatment facilitates a biomimetic introduction of cross-links in collagenous biopolymer systems, modifying their viscoelastic properties, mechanical stability, and swelling behavior. For reconstituted collagen type I fibers, electron-induced cross-linking opens up new perspectives regarding future biomedical applications in terms of tissue and ligament engineering. We demonstrate how electron irradiation affects stiffness both in low-strain regimes and in postyield regimes of biocompatible reconstituted rat tail collagen type I fibers. Stress-strain tests show a dose-dependent increase in modulus in the nonlinear elastic response, indicating a central role of induced cross-links in mechanical stability. Environmental scanning electron microscopy after fiber rupture reveals aligned distributed collagen fibril domains under the fiber surface for as-prepared fibers, accompanied by a ductile fracture behavior, whereas, in tensile tests imaged by light microscopy after 10 MeV electron treatment, isotropic network topologies are observed until the occurrence of a brittle type of rupture. Based on the biomimicry of the process, these findings might pave the way for a novel type of synthesis of tailored tendon or ligament substitutes.

Design and characterization of iron–calcium–aluminium–silicate–hydrate as low-temperature binder

This work aims to synthesize new cementitious materials (binders) using marble powder, rice husk ash, activated laterite and NaOH solution by applying low energy process. The binder was used to stabilize solid precursors (laterite and pozzolan). To achieve this objective, calcium–silicate–hydrate (CSH) was first synthesized at different temperatures (26, 50, 80 and 100 °C). The best physical–mechanical properties were chosen to produce iron–calcium–aluminium–silicate–hydrate [Fe–C(A)SH] at different concentrations of sodium hydroxide solution: 4, 5, 6 M. Finally, the formulated binder at 6 M of NaOH solution was used to stabilize laterite and pozzolans at the following proportions 20%, 30%, 40% and 50%. The samples were characterized after 28 days of curing at room temperature. FT-infrared spectroscopy, X-ray diffraction, and environmental scanning electron microscope ESEM-EDS permitted to confirm the formation of CSH, and Fe–C(A)SH. The mechanical test used to evaluate the performance showed that the incorporation of 10% iron-rich laterite into CSH increased the strength up to 42.93 MPa and the addition of Fe–C(A)SH in the laterite/pozzolans increased the compressive strength of the final product (15.34 and 15.8 MPa for laterite and pozzolan, respectively). The highest concentration (6 M) increases the alkalinity and reduces the efficiency of silicate polymerization affecting the final structural compound. From the results, low-energy Fe–C(A)SH-based cement and stabilized compounds appeared promising for the development of sustainable infrastructures.

Structure, ultrastructure and cation accumulation in quinoa epidermal bladder cell complex under high saline stress.

Quinoa is a facultative halophyte with excellent tolerance to salinity. In this study, the epidermal bladder cell complex (EBCc) of quinoa leaves was studied to determine their cellular characteristics and involvement in salt tolerance. We used light microscopy, confocal RAMAN microscopy, confocal fluorescence microscopy, transmission electron microscopy, and environmental scanning electron microscopy complemented by energy dispersive X-ray analysis. Ionic content was quantified with flame atomic absorption spectroscopy and with flame emission photometry. Results show that: (i) the number of EBCcs remains constant but their density and area vary with leaf age; (ii) stalk cells store lipids and exhibit thick walls, bladder cells present carotenes in small vesicles, oxalate crystals in vacuoles and lignin in their walls and both stalk and bladder cells have cuticles that differ in wax and cutin content; (iii) chloroplasts containing starch can be found on both stalk and bladder cells, and the latter also presents grana; (iv) plasmodesmata are observed between the stalk cell and the bladder cell, and between the epidermal cell and thestalkcell, and ectodesmata-like structures are observed on the bladder cell. Under high salinity conditions, (v) there is a clear tendency to accumulate greater amounts of K+ with respect to Na+ in the bladder cell; (vi) stalk cells accumulate similar amounts of K+ and Na+; (vii) Na+ accumulates mainly in the medullary parenchyma of the stem. These results add knowledge about the structure, content, and role of EBCc under salt stress, and surprisingly present the parenchyma of the stem as the main area of Na+ accumulation.

Impact of high hydrostatic pressure and ultrasounds technologies in the autolytic process of Saccharomyces cerevisiae in a model wine system

Autolysis plays a crucial role as a technological tool in the ageing process of specific wines. This includes white, red and sparkling wines. During ageing on the lees, yeasts release different compounds that positively modify the composition of the wine. However, traditional autolytic methods can be time-consuming. This work evaluates the use of different ultrasound (US) and high hydrostatic pressure (HHP) treatments to expedite the autolytic process in Saccharomyces cerevisiae in a model wine system. The results suggest that treating yeast cells with US resulted in a faster release of nucleic acids, proteins, and total polysaccharides compared to HHP treatment. The environmental scanning electron microscopy (ESEM) of the treated lees demonstrated that the impact on the yeast cell surface was more pronounced after exposure to US compared to treatments involving HHP. In conclusion, under these conditions the US treatment effectively triggered autolysis in the wine yeast strain, facilitating the release of macromolecules in a model wine.

Metastable nickel–oxygen species modulate rate oscillations during dry reforming of methane

AbstractWhen a heterogeneous catalyst is active, it forms metastable structures that constantly transform into each other. These structures contribute differently to the catalytic function. Here we show the role of different metastable oxygen species on a Ni catalyst during dry reforming of methane by combining environmental scanning electron microscopy, near ambient pressure X-ray photoelectron spectroscopy, on-line product detection and computer vision. We highlight the critical role of dissociative CO2 adsorption in regulating the oxygen content of the catalyst and in CH4 activation. We also discover rate oscillations during dry reforming of methane resulting from the sequential transformation of metastable oxygen species that exhibit different catalytic properties: atomic surface oxygen, subsurface oxygen and bulk NiOx. The imaging approach allowed the localization of fluctuating surface regions that correlated directly with catalytic activity. The study highlights the importance of metastability and operando analytics in catalysis science and provides impetus towards the design of catalytic systems.

Removal of pollutants from aquaculture wastewater using chitosan/bentonite composite beads

Aquaculture systems produce ammonia nitrogen as a by-product of aquatic animal protein metabolism. The dropwise method was used in this study to prepare composite beads based on the chitosan (CS) biopolymer and bentonite (Bt) clay to remove ammonia nitrogen from aquaculture wastewater. The composite beads were characterised using Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), Brunauer–Emmett–Teller analysis and environmental scanning electron microscopy. According to the FTIR analysis, CS was successfully immobilised on the surface of Bt. Furthermore, the XPS analysis revealed that the chemical surface of the chitosan/bentonite (CSBt) composite was rich in CS elements. To remove ammonia nitrogen, three samples of aquaculture effluents were collected and characterised in terms of physico-chemical and chemical aspects. The ammonia nitrogen removal from aquaculture effluents was 100, 91.8 and 87.7% for initial concentrations of 0.56, 1.72 and 2.13 mg/l, respectively. Ammonia nitrogen sorption tends to reach equilibrium in approximately 120 min. The findings also show that the kinetic data correlated well with the pseudo-second-order equation. pH values increased slightly after adsorption, and the same trend was observed for total hardness and alkalinity. As a result, the CSBt composite is a promising adsorbent for ammonia nitrogen removal from aquaculture effluents.

Microstructural Changes in Vanilla planifolia Beans after Using High-Hydrostatic-Pressure Treatment in the Curing Process.

During vanilla bean curing, the cell arrangement derived from the killing technique applied to start bean ripening is essential to obtain the characteristic aroma and flavor of vanilla. Hence, killing is an important step to release the enzymes and compounds required for vanillin production. In this work, high hydrostatic pressure (HHP) at 100-400 MPa for 5 min, using water at 7 °C as the pressure-transmitting medium, was applied as the killing method, and its effect on the microstructural changes in vanilla beans during different curing cycles (C0-C20) was evaluated and compared with that observed after scalding by using water at 100 °C for 8 s. Microstructural changes in the cross-sectioned beans were analyzed using a stereomicroscope (SM), confocal laser scanning microscopy (CLSM), and environmental scanning electron microscopy (ESEM). The vanilla beans were cross-sectioned and three main sectors were analyzed: the total, annular, and core. The morphometric descriptors, namely, area, Feret's diameter, and circularity, were quantified via digital image analysis (DIA), from which a shrinkage ratio was calculated. The results show that the total area in the beans presented a maximum decrease in the C16 of curing. The core area was most affected by the HHP treatment, mainly at 400 MPa, rather than scalding. CSLM observations revealed the autofluorescence of the compounds inside the beans. In conclusion, the use of microscopy techniques and DIA allowed us to determine the microstructural changes in the HHP-treated pods, which were found to be more numerous than those found in the scalded beans.

Advances in the application of proton transfer reaction mass spectrometry

With the continuous development of social science and technology, micro-area information has become an important part of modern material information research, environmental scanning electron microscope (ESEM) is a new type of scanning electron microscope (SEM) developed in recent years. ESEM follows the principle of scanning electron microscopy and uses high-energy electron beams to hit the surface of an object, transforming the surface morphology into electrical signals that characterize brightness. Compared to traditional scanning electron microscopes, ESEM does not require samples to be dry, clean, and conductive. In addition, it can also observe and analyse samples in atmospheric and other environments and is widely used in multiple disciplines such as life sciences, medicine, and materials science. Therefore, this paper introduces the composition and working principle of ESEM describes the basic features of ESEM, and introduces the applications of ESEM in different fields, aiming to provide a reference role for the development of ESEM.

Investigation of coated hydrophobic granular materials by means of computed tomography and environmental scanning electron microscopy

Hydrophobic materials in geotechnical engineering and soil science can have natural or artificial origin. They can be applied, e. g., to waterproof structures in the industry. In this contribution, hydrophobic granular material was manufactured through a cold plasma polymer coating procedure. The monomer used was C4F8 (octafluorocyclobutane) and the material to be coated was Hamburg sand, a coarse grained sand. In this context, computed microtomography and environmental scanning electron microscopy were used to investigate the materials in their unsaturated state. The tools are applied to visualize unsaturated phenomena on the microscale. The hydrophobic and untreated materials were imaged by both techniques at different saturation degrees in order to understand the influence of the coating on the sample’s hydraulic behaviour. The chosen environmental scanning electron microscope is able to provide relative humidity in the sample chamber, and so water drops were condensed on the grain surface, allowing to also observe the initial contact of water and the hydrophobic coating. It was observed how the capillary menisci, their geometry and contact properties evolve at different degrees of saturation. The measurements obtained and respective analyses state qualitatively the influence of the hydrophobic coatings on the pore water dynamics at different saturation degrees, which dictates the material’s hydraulic behaviour. Contact angles were also analysed were it was physically possible.

Microscopic visualization of heterogeneous condensation of water vapor on hydrophilic and hydrophobic particles

Heterogeneous condensation of water vapor on particles is widely used in the fields of atmospheric cloud physics and industrial particulate abatement. Particles surface wettability plays a fundamental role in water vapor condensation, but a microscopic insight of the impact of particles surface wettability on vapor condensation is lacked. Therefore, the Environmental Scanning Electron Microscope (ESEM) is adopted to directly visualize vapor condensation on particles with different surface wettability at a microscopic scale. Firstly heterogeneous condensation of water vapor on the hydrophilic and hydrophobic particles is obtained by the ESEM. The results show that when water vapor condenses on the hydrophilic particles, a spherical cap-shaped embryo first appears and subsequently develops into a spherical droplet to finally wrap the single particle. While on the hydrophobic particles, a spherical cap-shaped embryo will first appear and continue to grow into a spherical droplet to finally detach from the particle. Then the wetting coefficient is introduced to characterize the wetting degree of the droplet on the particle. The wetting coefficient will increase with the decrease of the contact angle, so the wettability of water vapor on the hydrophilic particles is better than that on the hydrophobic particles. Meanwhile based on classical nucleation theory, the geometrical factor and the critical supersaturation will decrease when the contact angle decreases, making it easier for water vapor to condense on the hydrophilic particles. Finally the line tension is investigated to explain the condensation mechanism. On the hydrophilic particles, when the droplet has crossed the equatorial line of the particle, the positive line tension promotes the spreading movement of the droplet over the particle to form a wrapped spherical droplet. Therefore, there is a transition from a spherical cap-shaped embryo before crossing the equatorial line of the particle to a wrapped spherical droplet after crossing the equatorial line. While on the hydrophobic particles, the negative line tension suppresses the spreading movement of the droplet over the particle to form a detached spherical droplet. So there is a transition from a spherical cap-shaped embryo before crossing the equatorial line of the particle to a detached spherical droplet after crossing the equatorial line.