Energy Dispersive X-ray Research Articles

Oleylamine-grafted carbon nanoparticles as the friction-reducing and anti-wear additives of aviation lubricating oils

Purpose This paper aims to try to develop new, environmentally friendly and efficient lubricating additives; study the compatibility of carbon-based additives with different base oils [Polyalphaolefin (PAO)-3, PAO-20 and NPE-2]; and explore the lubrication mechanism. Design/methodology/approach Oleylamine modified carbon nanoparticles (CNPs-OA) were prepared and the dispersion stability of CNPs-OA in PAO-3, PAO-20 and NPE-2 base oils was investigated by transmission electron microscopy, Fourier transform infrared, thermogravimetric analysis, energy dispersive spectroscopy and X-ray photoelectron spectroscopy. Universal Mechanical Tester (UMT) platform was used to carry out experiments on the effects of different additive concentrations on the lubricating properties of base oil. Findings The mean friction coefficient of PAO-3, PAO-20 and NPE-2 reduced by 32.8%, 10.1% and 11.4% when the adding concentration of CNPs-OA was 1.5, 2.0 and 0.5 Wt.%, respectively. Generally, The CNPs-OA exhibited the best friction-reducing and anti-wear performance in PAO-3. Originality/value The agglomeration phenomenon of carbon nanoparticles as lubricating additive was improved by surface modification, and the lubricating effect of carbon nanoparticles in three synthetic aviation lubricating base oils was compared.

Phytogenic Synthesis of Cuprous and Cupric Oxide Nanoparticles Using Black jack Leaf Extract: Antibacterial Effects and Their Computational Docking Insights

Background: Green synthesized nanoparticles (NPs) have gained increasing popularity in recent times due to their broad spectrum of antimicrobial properties. This study aimed to develop a phytofabrication approach for producing cuprous (Cu2O) and cupric oxide (CuO) NPs using a simple, non-hazardous process and to examine their antimicrobial properties. Methods: The synthesis employed Bidens pilosa plant extract as a natural reducing and stabilizing agent, alongside copper chloride dihydrate as the precursor. The biosynthesized NPs were characterized through various techniques, including X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier-transform infrared (FT-IR) spectroscopy, ultraviolet–visible (UV-Vis) spectroscopy, scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDS). Results: XRD analysis confirmed that the synthesized CuO and Cu2O NPs exhibited a high degree of crystallinity, with crystal structures corresponding to monoclinic and face-centered cubic systems. SEM images revealed that the NPs displayed distinct spherical and sponge-like morphologies. EDS analysis further validated the purity of the synthesized CuO NPs. The antimicrobial activity of the CuO and Cu2O NPs was tested against various pathogenic bacterial strains, including Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli, and Bacillus cereus, with the minimum inhibitory concentration (MIC) used to gauge their effectiveness. Conclusions: The results showed that the phytosynthesized NPs had promising antibacterial properties, particularly the Cu2O NPs, which, with a larger crystal size of 68.19 nm, demonstrated significant inhibitory effects across all tested bacterial species. These findings suggest the potential of CuO and Cu2O NPs as effective antimicrobial agents produced via green synthesis.

A FEM-based model for failure initiation in the microstructure of gray cast iron under uniaxial compression

PurposeThe purpose of this study was to validate the feasibility of the proposed microstructure-based model by comparing the simulation results with experimental data. The study also aimed to investigate the relationship between the orientation of graphite flakes and the failure behavior of the material under compressive loads as well as the effect of image size on the accuracy of stress–strain behavior predictions.Design/methodology/approachThis paper presents a microstructure-based model that utilizes the finite element method (FEM) combined with representative volume elements (RVE) to simulate the hardening and failure behavior of ferrite-pearlite matrix gray cast iron under uniaxial loading conditions. The material was first analyzed using optical microscopy, scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS) and X-ray diffraction (XRD) to identify the different phases and their characteristics. High-resolution SEM images of the undeformed material microstructure were then converted into finite element meshes using OOF2 software. The Johnson–Cook (J–C) model, along with a damage model, was employed in Abaqus FEA software to estimate the elastic and elastoplastic behavior under assumed plane stress conditions.FindingsThe findings indicate that crack initiation and propagation in gray cast iron begin at the interface between graphite particles and the pearlitic matrix, with microcrack networks extending into the metal matrix, eventually coalescing to cause material failure. The ferritic phase within the material contributes some ductility, thereby delaying crack initiation.Originality/valueThis study introduces a novel approach by integrating microstructural analysis with FEM and RVE techniques to accurately model the hardening and failure behavior of gray cast iron under uniaxial loading. The incorporation of high-resolution SEM images into finite element meshes, combined with the J–C model and damage assessment in Abaqus, provides a comprehensive method for predicting material performance. This approach enhances the understanding of the microstructural influences on crack initiation and propagation, offering valuable insights for improving the design and durability of gray cast iron components.

Scanning electron microscopy, morphometric and energy dispersive X-Ray analysis of cephalothoracic structures exploring defensive and sensory features in kuruma shrimp (Marsupenaeus japonicus Spence Bate, 1888)

Abstract Background Kuruma shrimp (Marsupenaeus japonicus) is a commercially important crustacean and a valuable global food source. This study employed scanning electron microscopy (SEM) to explore the morphology and morphometric features of the Marsupenaeus japonicus cephalothoracic structures, including antennules, antennas, scaphocerite, rostrums, and eye stalks. The primary focus was on understanding the role of each part, especially through the examination of setae, which are crucial for chemoreception and defense. Additionally, energy dispersive X-ray spectroscopy (EDX) analysis was utilized to identify the elemental composition of these structures. Material and methods The samples from the heads of fifteen Marsupenaeus japonicus were studied by gross morphology and morphometry, SEM, and EDX analysis. This study is the first to integrate both SEM and EDX techniques for a detailed analysis of these cephalothoracic structures, offering an innovative approach to understanding both morphological and elemental characteristics. Results Marsupenaeus japonicus exhibited two antennules and two antennae. The antenna featured four basal segments: basicerite, ischiocerite, merocerite, and carpocerite, each with distinctive articulations and setae distribution. The antennule, with three segments covered by plumose setae, displayed curved cone-shaped flagellae. The scaphocerite, resembling a paddle, showcased plumose setae, while the rostrum exhibited dorsal and ventral spines, lateral grooves, and unique setal arrangements. Setal measurements across structures revealed diverse lengths and widths, indicating functional specialization. The compound eyes were connected to an optic stalk adorned with plumose setae. EDX analysis revealed higher percentages of calcium and phosphorus in the spear-like structures of the scaphocerite, rostrum, and antenna, respectively. Conclusion This investigation provides a thorough examination of the intricate morphological features of the cephalothoracic region of Marsupenaeus japonicus, shedding light on its sensory and defensive capabilities. The novel application of both SEM and EDX not only deepens our insights into these structures but also lays the groundwork for future studies using this dual approach to explore crustacean morphology, with potential advantages for sustainable aquaculture and the conservation of marine ecosystems.

Nanocrystalline Lanthanum Oxide Layers on Tubes Synthesized Using the Metalorganic Chemical Vapor Deposition Technique

Lanthanum oxide (La2O3) layers are widely used in electronics, optics, and optoelectronics due to their properties. Lanthanum oxide is also used as a dopant, modifying and improving the properties of other materials in the form of layers, as well as having a large volume. In this work, lanthanum oxide layers were obtained using MOCVD (Metalorganic Chemical Vapor Deposition) on the inner walls of tubular substrates at 600–750 °C. The basic reactant was La(tmhd)3 (tris(2,2,6,6-tetramethyl-3,5-heptanedionato)lanthanum(III)). The evaporation temperature of La(tmhd)3 amounted to 170–200 °C. Pure argon (99.9999%) and air were used as the carrier gases. The air was also intended to remove the carbon from the synthesized layers. Tubes of quartz glass were used as the substrates. La2O3 layers were found to be growing on their inner surfaces. The value of the extended Grx/Rex2 criterion, where Gr—Grashof’s number, Re—Reynolds’ number, x—the distance from the gas inflow point, was below 0.01. The microstructure of the deposited layers of lanthanum oxide was investigated using an electron scanning microscope (SEM). Their chemical composition was analyzed via energy-dispersive X-ray (EDS) analysis. Their phase composition was tested via X-ray diffraction. The transmittance of the layers of lanthanum oxide was determined with the use of UV-Vis spectroscopy. The obtained layers of lanthanum oxide were characterized by a nanocrystalline microstructure and stable cubic structure. They also exhibited good transparency in both ultraviolet (UV) and visible (Vis) light.

Marine Geo-Polymer Cement Treated with Seawater, Alkaline Activators, Recycled Particles from Paste, and Recycled Particles from Glass

This study aims to develop the marine geo-polymer cement that was produced with seawater, recycled particles from paste, recycled particles from glass, and alkaline activators, including NaOH or Na2O·3.3SiO2. The physicochemical properties and strength of MGPC were investigated with a Uniaxial Compression Test, Particle Size Analysis, Energy Dispersive Spectrometer, X-ray Diffraction, and Thermal-field Emission Scanning Electron Microscopy. The results indicated that the main hydration products in MGPC were calcium carbonate (CaCO3), silica (SiO2), sodium aluminosilicate hydrate (Na2O·Al2O3·xSiO2·2H2O, N-A-S-H), and aluminum calcium silicate hydrate (CaO·Al2O3·2SiO2·4H2O, C-A-S-H). The calcium carboaluminate (3CaO·Al2O3·CaCO3·32H2O, CO3-AFm) in MGPC was converted into CaCO3 and Friedel’s salt (3CaO·Al2O3·CaCl2·10H2O), which prompted the carbon sequestration. The microstructure of MGPC prepared using Na2O·3.3SiO2 was based on RPG as the matrix, with N-A-S-H, C-A-S-H, and fibrous AFt growing on the periphery. This structure reduces the impact of the alkali–silica reaction on the material and improves its compressive strength. Therefore, the MGPC developed in this study shows the exact benefits of freshwater and natural minerals saving, carbon sequestration, and damage resistance.

Novel Syntheses of Wide-Band Gap Semiconducting CdxZnx−1Co2O4 of Spinel Nanostructure: Characterization and Optical Properties

AbstractCadmium doped zinc cobaltite spinel structure in the form of CdxZnx-1Co2O4 (0 ≤ x ≤ 1) are synthesized by sol-gel method. The energy dispersive X-ray spectra confirm the synthesis of pure ZnCo2O4 and Cd doped samples nanoparticles. Scanning and transmission electron microscopes images of Cd ZnCo2O4 samples show the cubic crystal structure of the nanoparticles. A good crystallinity of the ZnCo2O4 and its dopants samples are indicated by the sharpness and strong peaks of X-ray diffraction patterns. The particle size is independent of the ratio of incorporated Cd into the ZnCo2O4 matrix. The FT-IR transmission spectrum of each Cdx Zn1-xCo2O4 complex shows two strong vibration peaks that are ascribed to the spinel structure’s octahedral and tetrahedral. The absorption spectra reveal three distinct absorption characteristics for Cdx Znx-1Co2O4 peaking at 268, 532 and 778 nm due to the photoexcitation of electrons from O 2p to Co 3d transitions and d-d transition of Co 3d. N2 adsorption–desorption isotherms for Cdx Znx-1Co2O4 indicate are carried out.

Antiseptic Surface Based on Antibacterial Polyethylene Composites with Silver Fillers: Stability in Aqueous Solution

One method to reduce the spread of pathogens is to use clean surfaces. These have long-acting components, and their use would reduce the massive consumption of disinfectants and cleaning products. In order to ensure the safety of these surfaces in water-based systems and prevent mishandling and potential health and environmental risks, this study analyzed the stability of clean surfaces made of polyethylene with three silver compounds with different water solubility. The surfaces were subjected to erosion at 40 °C by immersing them in aqueous solutions of 3% acetic acid (w/v), 50% ethanol (v/v), and deionized water. The ionic silver release was monitored in real-time in situ via voltammetry using an Ag/S2− electrode. Analytical methods such as Scanning Electron Microscopy (SEM) and Energy Dispersive X-ray Spectroscopy (EDS) were employed to elucidate the surface alteration. The plastic residue after immersion varied depending on the pH and the type of solvent used, with a higher plastic migration observed when in contact with the water-ethanol mixture. Furthermore, a correlation was identified between surface stability, oxygen composition in the antibacterial, and water solubility, influencing increased surface oxidation.

From STEM-EDXS data to phase separation and quantification using physics-guided NMF

Abstract We present the development of a new algorithm which combines state-of-the-art energy-dispersive X-ray (EDX) spectroscopy theory and a suitable machine learning formulation for the hyperspectral unmixing of scanning transmission electron microscope EDX spectrum images. The algorithm is based on non-negative matrix factorization (NMF) incorporating a physics-guided factorization model. It optimizes a Poisson likelihood, under additional simplex constraint together with user-chosen sparsity-inducing and smoothing regularizations, and is based on iterative multiplicative updates. The fluorescence of X-rays is fully modeled thanks to state-of-the-art theoretical work. It is shown that the output of the algorithm can be used for a direct chemical quantification. With this approach, it is straightforward to include a priori knowledge on the specimen such as the presence or absence of certain chemical elements in some of its phases. This work is implemented within two open-source Python packages, espm and emtables, which are used here for data simulation, data analysis and quantification. Using simulated data, we demonstrate that incorporating physical modeling in the decomposition helps retrieve meaningful components from spatially and spectrally mixed phases, even when the data are very noisy. For synthetic data with a higher signal, the regularizations yield a tenfold increase in the quality of the reconstructed abundance maps compared to standard NMF. Our approach is further validated on experimental data with a known ground truth, where state-of-the art results are achieved by using prior knowledge about the sample. Our model can be generalized to any other scanning spectroscopy techniques where underlying physical modeling can be linearized.

Enhanced corrosion protection of copper in saline environments using bio-nanocomposite coatings based on chitosan and chitosan Schiff base

An in-depth study focuses on developing new environmentally friendly bio-nanocomposites, by incorporating SrTiO3 (STO) ceramic nanoparticles into matrices of chitosan and its derivatives, aiming to use them as protective coatings against corrosion. The various stages of this study include the cross-linking of chitosan, the synthesis of Schiff base chitosan, the cross-linking of Schiff base chitosan, and the preparation of nanocomposite coatings. The coatings' structure and composition were analyzed using different methods, including Fourier Transform Infrared Spectroscopy - Attenuated Total Reflectance (FTIR-ATR), X-ray Diffraction (XRD), Transmission Electron Microscopy coupled with Energy Dispersive X-ray Spectroscopy (TEM-EDX), and Scanning Electron Microscopy (SEM). In addition, Electrochemical Impedance Spectroscopy (EIS) and Potentiodynamic Polarization (PDP) measurements were carried out to assess the inhibitory efficacy of chitosan crosslinked with epichlorohydrin (Cs-Ep), epichlorohydrin-crosslinked chitosan-salicylaldehyde Schiff base (CS-S-Ep) and CS-Ep-STO and CS-S-Ep-STO nanocomposite coatings, as well as the long-term protection durability of CS-S-Ep-STO. These techniques revealed a significant reduction in corrosion current density after chemical modification of chitosan and incorporation of SrTiO3 (STO) nanoparticles into CS-Ep and CS-S-Ep matrices, confirming a notable improvement in the inhibitory efficiency of these coatings against copper corrosion in a saline environment. Computational modeling methods like Density Functional Theory (DFT), Molecular Dynamics (MD), and Monte Carlo (MC) simulations reinforced these results by demonstrating efficient adsorption of CS-S-Ep-STO nanocomposites on metal surfaces through the interaction with heteroatoms present in the functional groups (-C=N-, -C-O-, -OH) and STO nanoparticles. The present study's findings provide key information for developing innovative protective coatings, highlighting the potential of chitosan-based nanocomposites and derivatives, particularly with SrTiO3 incorporation, in mitigating metal surface corrosion in aggressive environments.

Exploring Pt-Impregnated CdS/TiO2 Heterostructures for CO2 Photoreduction

This work focuses on the production of methane through the photocatalytic reduction of carbon dioxide using Pt-doped CdS/TiO2 heterostructures. The photocatalysts were prepared using P25 commercial titania and CdS synthesized through a solvothermal methodology, followed by the impregnation of Pt onto the surface to enhance the physicochemical properties of the resulting photocatalysts. The pure and heterostructure-based materials were characterized using X-ray diffraction (XRD), inductively coupled plasma optical emission spectroscopy (ICP-OES), scanning electron microscopy (SEM) with energy dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), ultraviolet-visible spectroscopy (UV-Vis), ultraviolet photoelectron spectroscopy (UPS), and photoluminescence spectroscopy (PL). The obtained results show the successful synthesis of the heterostructure impregnated with Pt. Moreover, the observed key role of CdS and Pt nanoparticles in the final semiconductor is to reduce the electron-hole pair recombination rate by acting as an electron sink, which slows down the recombination process and increases the photocatalyst efficiency. Thus, Pt-doped CdS/TiO2 heterostructures with the best observed composition presents better catalytic activity than P25 titania with methane production values being 460 and 397 µmol CH4/g·h, respectively.

Morphological and structural analysis of monodispersive silica nanoparticles fabricated by stober method for self-cleaning applications

Abstract In this work, silica nanoparticles have been synthesized via the Stober process on a p-type silicon substrate by spin coating method. Structural and morphological studies have been carried out by x-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM). Microstructural analysis by Raman spectroscopy displays a prominent peak at 524 cm−1 which corresponds to crystalline silicon. Further, the elemental study by using energy dispersive x-ray spectroscopy (EDX) confirms the presence of silica with no other impurities. Besides, the wettability property has been studied by contact angle measurement and found to be around 130° for the 6-layer coated thin film which is quasi-super-hydrophobic. The wettability results obtained signify promising properties for the development of self-cleaning devices and applications.

Effect of agitation during the early-age hydration on thixotropy and morphology of cement paste

AbstractThe effect of agitation during the early-age hydration on thixotropy and morphology of cement paste prepared with and without superplasticizers (SP) is investigated by applying penetration test, small amplitude oscillatory shear sweep test (SAOS), isothermal calorimetric test, scanning electron microscopy (SEM) and energy dispersive X-ray analyses (EDX). The results show that the agitation of cement paste during the induction period increases the heat flow rate and destroys existing structures of samples without changing the mineral composition of samples. Yet, if the agitation is applied during the acceleration period, the heat flow rate is significantly lowered and the morphology and mineral composition of samples undergo irreversible change, freshly formed syngenite is destroyed and no longer restored. The penetration force and the static yield stress grow linearly during the induction period and exponentially during the acceleration period. Agitation during the induction period destroys the structure, which causes the static yield stress and the penetration force values becoming nearly equal to zero. However, during the acceleration period, even after agitation the static yield stress and the penetration force exhibit high residual values, which indicates the impact of hydration to the structural build-up.

Efficient Removal of Cu(II) and Ni(II) Ions from Aqueous Solutions Using Reduced Graphene Oxide/Bentonite Clay/ZnO Nanocomposites: Kinetics, Mechanisms, and Adsorption Performance

<p style="text-align:justify;text-indent:36.0pt;"><span style="font-family:"Arial","sans-serif";font-size:11pt;line-height:150%;">To assess the efficacy of removing heavy metals such as Cu (II) and Ni (II) ions from aqueous solution, the adsorption behaviour of a nanocomposite powder comprising of reduced Graphene Oxide (rGO), bentonite clay, and ZnO was investigated. Various analytical techniques including Fourier transform infrared spectroscopy, Field emission scanning electron microscopy, Energy-Dispersive X-ray spectroscopy, X-Ray diffraction analysis, and N<sub>2</sub> adsorption/desorption analysis were utilized to analyse the synthesized composites. Through the batch equilibrium approach, parameters influencing adsorption behaviours, including initial metal ion concentration, pH, adsorbent dosage, and contact time, were comprehensively examined. Adsorption data were shown to have good fit to the Langmuir isotherm model and pseudo-first-order model, with high R<sup>2</sup>, low root mean square error (RMSE), low chi square (Χ<sup>2</sup>), and low standard deviation (SD) values when using the linear regression approach. For the raw sample (rGO/ bentonite clay) containing copper and nickel, equilibrium was achieved in 80 minutes, while for samples with 1% (rGO/ bentonite clay/1% ZnO), 3% (rGO/ bentonite clay/3% ZnO), and 5% (rGO/ bentonite clay/5% ZnO), equilibrium was attained within 70 minutes. </span><span style="background-color:white;font-family:"Arial","sans-serif";font-size:11pt;line-height:150%;">Within the pH range of 2 to 12, the adsorption kinetics of copper and nickel exhibited a notable pH-dependent relationship, highlighting the pronounced influence of pH conditions on the adsorption process</span><span style="background-color:white;color:#374151;font-family:"Segoe UI","sans-serif";font-size:11pt;line-height:150%;">. </span><span style="background-color:white;font-family:"Arial","sans-serif";font-size:11pt;line-height:150%;">Copper consistently demonstrated superior removal efficiency compared to nickel in all conducted adsorption tests, attributed to its heightened propensity for bond formation with adsorbent surfaces.</span><span style="font-family:"Arial","sans-serif";font-size:11pt;line-height:150%;"> The primary pathways for copper and nickel adsorption on the composites involved intermolecular interactions, cation exchange, physisorption and electrostatic interactions. The Langmuir model revealed maximum Cu (II) adsorption capacities of 312.5 mg/g, 217.39 mg/g, 161.95 mg/g, and 101.96 mg/g for raw sample, 1%, 3%, and 5% samples, respectively. Nickel (II) adsorption capacity were measured at 252.41 mg/g, 185 mg/g, 125.03 mg/g, and 96.60 mg/g for the raw sample, 1%, 3%, and 5% samples, respectively.</span></p>

Adsorption of Arsenic and Cadmium on Biodegradable and Non-Biodegradable Microplastics in Soil: Comparison Based on Batch Experiment

In the present study, the adsorption of arsenic(V) and cadmium(II) onto microplastics from poly(butylene succinate-co-butylene adipate) (PBSA) and low-density polyethylene (LDPE) plastic mulch films was investigated through batch experiment. The surface morphology and elemental composition of soil and microplastics were analyzed with scanning electron microscopy equipped with energy-dispersive X-ray spectroscopy (SEM-EDX) and Fourier-transform infrared (FTIR) spectroscopy. The results show that the adsorption of As(V) and Cd(II) on microplastics led to surfaces with coarseness and more cracks, and many small particles. Under the conditions added with 100 pieces of microplastic, PBSA enhanced the adsorption capacity of As(V) (from 0.43 to 0.49 mg/g), and LDPE increased the adsorption of Cd(II) (from 0.174 to 0.176 mg/g) due to the “superimposed effect” caused by hydrogen bonds. Conversely, LDPE reduced the adsorption of As(V) (from 0.44 to 0.40 mg/g) due to a “dilution effect” of PE. Particularly, PBSA exhibited an insignificant effect on the adsorption of Cd(II) in soil during the present study. Overall, our findings provide new insights into the impacts of microplastics on the fate and behavior of heavy metals in the soil system.

Metal Contamination and Human Health Risk Assessment of Soils from Parks of Industrialized Town (Galati, Romania)

The aim of the present study was to evaluate the contamination state of the surface soil from 10 parks from Galati, Romania, and the health hazards of the soil. The soil samples, collected in each site from the playing ground and from the edge of the park, were analyzed by using combined Wavelength- (WDXRF) and Energy-Dispersive (EDXRF) X-ray fluorescence techniques. A total number of 27 chemical elements (Ag, Al, As, Ba, Ca, Cd, Cr, Co, Cu, Fe, Hg, K, Mg, Mn, Na, Ni, P, Pb, Rb, Sb, Sc, Sn, Sr, Ti, V, Zn and Zr) were quantified in the urban soils, and the results were compared to the normal and alert values from Romanian legislation for toxic trace elements, as well as with European and world average values of element concentrations. The mineralogical analyses were performed by Scanning Electron Microscopy with Energy-Dispersive X-ray Analysis (SEM-EDX) and the Attenuated Total Reflectance–Fourier Transform Infrared technique (ATR-FTIR). To assess the soil contamination and the impact on human health of the presence of potential toxic elements and heavy metals in the soil, a series of pollution and health risk indices were used. All the results indicated an unpolluted to moderately polluted soil. The soil samples collected from the edge of the parks presented higher values for the specific pollutants, which originated from heavy traffic, such as Cu, Cr, Zn and Pb. The non-carcinogenic and carcinogenic risk to children was assessed using estimated daily intake (EDI) in relation to the pathways whereby pollutants can enter the human body, such as ingestion, dermal contact, inhalation and vaporization. Using the obtained values for EDI, the hazard quotient and hazard index were determined, which strengthen the formerly issued presumption that soil pollution is moderate and, by itself, does not present any threat to children’s health.

Effect of Co Addition on the Microstructure and Mechanical Properties of Sn-11Sb-6Cu Babbitt Alloy

A Babbitt alloy SnSb11Cu6 with 0–2.0 wt.% Co was synthesized using the induction melting process. This study examined the effect of cobalt (Co) on the microstructure, tensile properties, compressive properties, Brinell hardness, and wear properties of SnSb11Cu6 using optical microscopy (OM), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), a universal tensile testing machine, a Brinell hardness tester, and a wear testing machine. The results indicate that the optimal quantity of Co can enhance the microstructure of the Babbitt alloy and promote microstructure uniformity, with presence of Co3Sn2 in the matrix. With the increase in Co content, the tensile and compressive strength of the Babbitt alloy first increased and then decreased, and the Brinell hardness gradually increased with the increase in Co content. The presence of trace Co has a minimal effect on the dry friction coefficient of the Babbitt alloy. When the Co content exceeds 1.5 wt.%, the friction properties of the Babbitt alloy deteriorate significantly. The optimized Babbitt alloy SnSb11Cu6-1.5Co was subsequently fabricated into wires, followed by conducting cold metal transfer (CMT) surfacing experiments. The Co element can promote the growth of interfacial compounds. The microstructure at the interface of the Babbitt alloy/steel is dense, and there is element diffusion between it. The metallurgical bonding is good, and there are serrated compounds relying on the diffusion layer to extend to the direction of the additive layer with serrated compounds extending and growing from the diffusion layer to the additive layer. Overall, Babbitt alloys such as SnSb11Cu6 exhibit improved comprehensive properties when containing 1.5 wt.% Co.

Low-cost bacterial cellulose production from agricultural waste for antibacterial applications

Various carbon sources can be utilized for the biosynthesis of bacterial cellulose (BC), with agricultural wastes being explored as sustainable options. In this study, glucose was extracted from bamboo dust via mild acid hydrolysis to prepare a modified medium combining extracted glucose with Hestrin-Schramm (HS) medium for BC biosynthesis using Acetobacter xylinus NCIM 2526. Chitosan, a biopolymer, was incorporated into the BC synthesis medium at concentrations of 0.2%, 0.6%, and 1% (w/v) after 2 days of shaking incubation, producing chitosan-incorporated BC membranes through in situ synthesis. Fourier transform infrared (FTIR) spectroscopy confirmed cellulose in the BC produced from the modified medium and chitosan in BC membranes with 0.2% and 0.6% (w/v) chitosan. Changes in physical and crystalline morphology were further characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD) analysis. The purity of cellulose was validated through chemical solubility tests, while energy-dispersive X-ray (EDX) analysis confirmed the presence of chitosan in the BC membranes. The average yields were 5.8 ± 0.21 g/l for pure BC, 5.2 ± 0.21 g/l for BC with 0.2% (w/v) chitosan, and 4.6 ± 0.21 g/l for BC with 0.6% (w/v) chitosan after 7 days. The medium with 1% (w/v) chitosan did not produce BC membranes. BC synthesized with 0.2% chitosan exhibited similar physical and chemical properties to pure BC and demonstrated good antimicrobial properties, suggesting its potential use in bandages and wound dressings.

Multiscale characterisation on the adhesion and selective adsorption at bitumen–mineral interface

The adhesion between bitumen and minerals is essential for the durability of asphalt mixtures, influenced by bitumen composition and mineral structure. The chemical action theory suggests that polar components in bitumen are adsorbed onto the mineral surface, facilitating adhesion. In this study, environmental scanning electron microscopy with energy-dispersive X-ray (ESEM-EDS) is used to analyse bitumen–mineral interfaces at a microscopic level. Elemental analysis reveals selective adsorption of polar substances from bitumen onto the surfaces of four types of minerals. Results show that alkaline rocks (limestone and albite) have a higher adsorption capacity than acidic rocks (granite and quartz). Additionally, treating mineral surfaces with alkaline solutions enhances adsorption. The adhesion properties of bitumen to various minerals are evaluated using the pull-off test. The correlation between ESEM-EDS and pull-off tests demonstrates that the macroscopic adhesion of bitumen to minerals is linked to the microscopic selective adsorption of polar substances.

Microstructures, crystallography and growth patterns of serpulid tubeworms (Class Polychaeta)

Serpulid polychaetes are marine worms that secrete calcium carbonate tubes in which they live. Despite extensive previous research on their microstructures, there are no crystallographic data and their biomineralization process remains unclear. Here, the microstructures of the tubes of seven serpulid species were studied, including their chemical composition, mineralogy and crystallography, using X-ray diffraction, Raman and Fourier transform infrared spectroscopy, scanning electron microscopy, energy dispersive X-ray spectroscopy, focused ion beam, electron backscatter diffraction, and thermogravimetric analysis. Generally, serpulid tubes have a high amount of organic matter (~ 7.5 wt%), consisting of chitin and proteins, and the calcite is always present as medium to high magnesium calcite. Three main microstructures were identified: granular-prismatic and lamello-fibrillar calcite, and fibrous aragonite. They all displayed an axial texture, which is stronger in the lamello-fibrillar calcite, with the c-axis aligned with the elongation axis of the crystals. These findings demonstrate that only some instances of the granular-prismatic and the lamello-fibrillar calcite are biogenic (primary) microstructures. Conversely, other instances of the granular-prismatic calcite and the fibrous aragonite are a consequence of a recrystallization process (i.e. secondary). Replacement may occur on either primary or secondary calcitic microstructures (replaced by aragonite). Secondary microstructures retain remnants of the previously replaced microstructures, such as vestigial crystals or major growth increments. The high-Mg nature of the calcite favors recrystallization. The plywood arrangement of the lamello-fibrillar calcite is hypothesized to result from the ordering of a chitin fibrillar precursor into a cholesteric liquid crystal phase, with the calcite subsequently growing by oriented nucleation onto the organic fibrils.