Scanning Electron Microscopy-energy Dispersive X-ray Spectroscopy Research Articles

Unveiling a novel exopolysaccharide produced by Pseudomonas alcaligenes Med1 isolated from a Chilean hot spring as biotechnological additive

Exopolysaccharides (EPSs), a constitutive part of bacterial biofilm, act as a protecting sheath to the extremophilic bacteria and are of high industrial value. In this study, we elucidate a new EPS produced by thermotolerant (growth from 34–44 °C) strain Pseudomonas alcaligenes Med1 from Medano hot spring (39.1 °C surface temperature, pH 7.1) located in the Central Andean Mountains of Chile. Bacterial growth was screened for temperature tolerance (10–60 °C) to confirm the thermotolerance behaviour. Physicochemical properties of the EPS were characterized by different techniques: Scanning Electron Microscopy- Energy Dispersive X-ray Spectroscopy (SEM-EDS), Atomic Force Microscopy (AFM), High-Performance Liquid Chromatography (HPLC), Gel permeation chromatography (GPC), Fourier Transform Infrared Spectroscopy (FTIR), Nuclear Magnetic Resonance (NMR), and Thermogravimetric analysis (TGA). Whole genome of P. alcaligenes Med1 has also been studied in detail to correlate the structural and functional characteristics with genomic insight. The EPS demonstrated amorphous surface roughness composed of evenly distributed macromolecular lumps composed of mainly carbon and oxygen. The monosaccharide analysis has shown the presence of glucose, galactose, and mannose sugars at different ratios. TGA revealed the high thermal stability (315.3 °C) of the polysaccharide. The GPC has shown that Med1 is a low molecular weight polysaccharide (34.8 kDa) with low PI. The 2D-NMR linkage analysis suggests a diverse array of glycosidic bonds within the exopolysaccharide structure. The functional properties of the EPS were evaluated for food industry applications, specifically for antioxidant (DPPH, FRAP an H2O2). Extracted Med1 EPS revealed significant emulsification activity against different food grade vegetative oils (Coconut oil, Corn oil, Canola oil, Avocado oil, Sunflower oil, Olive oil, and Sesame oil). The highest 33.9% flocculation activity was observed with 60 mg L−1 EPS concentration. It showed water-holding (WHC) of 107.6% and oil-holding (OHC) capacity of 110.8%. The functional EPS produced by Pseudomonas alcaligenes Med1 from Central Andean Chilean hot spring of central Chile can be a useful additive for the food-processing industry.

Safety and security of household water purifiers against pathogenic microbial contamination and bio-risk evaluation of their microbial community structures

Household water filters, particularly point-of-use systems, are crucial to ensure safe drinking water consumption by eliminating microbial contaminants. This study evaluated the efficacy of three types of water purifiers (ultrafiltration [UF], nanofiltration [NF], and reverse osmosis [RO]) against microbial contamination. In our experiments, Escherichia coli and bacteriophage MS2 were used as two microbial indicators in daily household settings to track the spatial and temporal profiles of their behavior from the filter inlets to in-UF, NF, and RO water purifiers, and then to effluents. The results showed that both NF and RO water purifiers removed 100 % of the indicator organisms. The UF water purifier achieved 100 % removal of E. coli, but the removal of MS2 phage was poor. The presence of coexisting ions and natural organic matter in tap water can significantly affect the behavior of MS2 phages during the water treatment process. Their presence reduces the charge repulsion effect of the UF membrane on the MS2 phage as well as promotes the migration of the MS2 phage on the post-activated carbon cartridge that was placed in the last unit of the water purifier system, which could increase the pathogen transmission risks in drinking water supplies. The bacterial community structures of the cartridge materials and cartridge effluents from each unit were analyzed by 16S rRNA gene sequencing, which revealed distinct microbial profiles of the different purifiers. Environmental conditions such as pH, nutrient availability, materials, and operational parameters can affect the composition of bacterial communities. Scanning electron microscopy-energy-dispersive X-ray spectroscopy (SEM-EDS) was used to examine the surface morphology of the membranes after they were exposed to water contaminants, which demonstrated that the inherent differences in the membrane structure influenced the retention of pollutants and microorganisms on the surfaces. In summary, this study demonstrates that both NF and RO water purifiers can significantly reduce the presence of various enteric and opportunistic pathogenic bacteria in drinking water, leading to safer potable water, whereas UF water purifiers may have certain risks owing to their UF membranes and post-activated carbon. In addition, secondary microbial contamination may be introduced by the post-activated carbon units of water purifiers, especially after long-term usage. Therefore, we concluded that addressing the secondary microbial pollution caused by post-activated carbon after prolonged use and long-term shutdown is essential for maintaining the safety and quality of drinking water.

DIFFUSE PUNCTATE DEPOSITS ON THE SURFACE OF HYDROPHILIC ACRYLIC INTRAOCULAR LENSES EARLY POSTOPERATIVELY: CASE SERIES AND LABORATORIAL ANALYSES

Purpose: To describe cases of hydrophilic acrylic intraocular lenses (IOLs) (Eyecryl, Biotech) exhibiting surface punctate deposits early postoperatively, and provide laboratorial analyses of unused lenses of the same model. Setting: Altino Ventura Foundation (FAV), Recife, Brazil, and John A. Moran Eye Center, University of Utah, Salt Lake City, Utah, USA. Design: Observational, descriptive, clinical study with laboratorial analysis. Methods: A thorough review of records of patients undergoing phacoemulsification with Eyecryl implantation in December 2022 at FAV was performed, with data collection. Five Eyecryl IOLs (never implanted/unused) were removed from the original package and underwent gross examination, light microscopy, and ultrastructural analyses using scanning electron microscopy/energy dispersive X-ray spectroscopy (SEM/EDS). Results: Details on 5 clinical cases exhibiting surface IOL deposits on the first postoperative day after uneventful surgery, and followed for at least 6 months were included. The deposits disappeared by the 60th postoperative day. No inflammatory or toxic reactions were noted, visual outcomes were favorable, and IOL explantation was not necessary. Three of the 5 unused lenses undergoing laboratorial analyses revealed diffuse, star-like shaped deposits that could not be removed by thorough irrigation with distilled water. SEM/EDS revealed a composition of the deposits that primarily consisted of carbon and oxygen. Conclusion: Laboratorial findings suggest the etiology of the deposits might be related to the manufacturing/packaging process of lenses from specific lots. While the deposits did not appear to be associated with inflammatory or toxic reactions in the clinical cases, further investigations are necessary to elucidate their precise origin.

Removal of Pb(II) and Cd(II) from a Monometallic Contaminated Solution by Modified Biochar-Immobilized Bacterial Microspheres.

Lead (Pb) and cadmium (Cd) are toxic pollutants that are prevalent in wastewater and pose a serious threat to the natural environment. In this study, a new immobilized bacterial microsphere (CYB-SA) was prepared from corn stalk biochar and Klebsiella grimontii by sodium alginate encapsulation and vacuum freeze-drying technology. The removal effect of CYB-SA on Pb(II) and Cd(II) in a monometallic contaminated solution was studied. The results showed that the removal of Pb(II) and Cd(II) by CYB-SA was 99.14% and 83.35% at a dosage of 2.0 g/L and pH = 7, respectively, which was 10.77% and 18.58% higher than that of biochar alone. According to the Langmuir isotherm model, the maximum adsorption capacities of Pb(II) and Cd(II) by CYB-SA at 40 °C were 278.69 mg/g and 71.75 mg/g, respectively. A combination of the kinetic model, the isothermal adsorption model, scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDS), X-ray photoelectron spectroscopy (XPS) and Fourier-transform infrared spectroscopy (FTIR) analyses showed that the main adsorption mechanisms of CYB-SA encompass functional group complexation, ion exchange, electrostatic attraction and physical adsorption. The findings of this study offer practical and theoretical insights into the development of highly efficient adsorbents for heavy metals.

Long-term Chinese milk vetch incorporation promotes soil aggregate stability by affecting mineralogy and organic carbon

Soil aggregates profoundly impact soil sustainability and crop productivity, and they are influenced by complex interactions between minerals and organics. This study aimed to elucidate the alterations in mineralogy and soil organic carbon (SOC) following long-term green manure incorporation and the effect on soil aggregates. Based on 5- and 36-year field experiments, surface soil samples (0-20 cm) were collected from Alfisol and Ferrisol soils subjected to rice-rice-winter fallow (CK) and rice-rice-Chinese milk vetch (MV) treatments to investigate aggregate stability, mineralogy, SOC composition, and soil microstructural characteristics. The results showed that high clay-content Ferrisol exhibited greater aggregate stability than low clay-content Alfisol. The phyllosilicates in Alfisol primarily comprised illite and vermiculite, whereas those in Ferrisol with high-content free-form Fe oxides (Fed) were dominated by kaolinite. Additionally, the clay fraction in Ferrisol contained more aromatic-C than the clay fraction in Alfisol. The 36-year MV incorporation significantly increased the Ferrisol macroaggregate stability (9.57-13.37%), and it also facilitated the transformation of vermiculite into kaolinite and significantly increased the clay, Fed, and aromatic-C contents in Ferrisol. Backscattered electron (BSE)-scanning electron microscopy/energy dispersive X-ray spectroscopy (SEM/EDS) revealed a compact aggregate structure in Ferrisol with co-localization of Fe oxides and kaolinite. Moreover, the partial least path model (PLS-PM) revealed that clay content directly improved macroaggregate stability, and that kaolinite and Fed positively and directly affected clay or indirectly modulated clay formation by increasing the aromatic-C levels. Overall, long-term MV incorporation promotes clay aggregation by affecting mineral transformation to produce more kaolinite and Fe oxides and retain aromatic-C, and it ultimately improves aggregate stability..

The effect of thermal aging on microhardness and SEM/EDS for characterisation bioactive filling materials

BackgroundThe aim of this study is to evaluate the surface microhardness, surface chemical composition of bioactive restorative materials pre- and post- thermal aging.MethodA total of 200 disc-shaped samples were prepared by using the materials: Cention N, ACTIVA BioActive Restorative, Equia Forte HT Fil, Glass Fill glass carbomer cement (GCP), and Fuji II LC. Vickers microhardness test were used to measure surface hardness. Scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM/EDS) was used to determine the characterization of the microstructures and elemental analysis of the materials. These measurements were repeated after thermal aging. One-Way ANOVA test, Bonferroni test and the Games-Howell test was used for data analysis. The significance level was accepted as 0.05.ResultsCention N had the highest vickers microhardness value before thermal cycle. The highest fluoride ion ratio among the materials before thermal aging was detected in the Equia Forte HT Fil and Fuji II LC groups. While a decrease in fluorideF ion was detected in all groups except the Cention N group after thermal aging. It is observed that ACTIVA BioActive Restorative has a more microporous and rougher surface in the scanning electron microscopy image after the thermal cycle than in the image before the thermal cycle.ConclusionsThe chemical properties of the materials and the properties of the filler particles may be related to the differences in the mechanical properties, surface characterizations and ion releases of the materials Thermal aging affected the microhardness, surface characteristics and elemental mass ratios of the studied materials. Alkasite bioactive materials are more similar to composite restorative materials and show better mechanical properties than other materials, but do not have the same effect on fluoride release.Clinical relevanceMost of the bioactive materials showed a decrease in the fluoride ion ratio after thermal aging, while no difference was found in the ion exchange of alkasite materials. Material selection should be made more carefully in caries-active individuals whose fluoride release is clinically important.

A facile synthesis procedure for Engelhard titanosilicate (ETS-4) and its Cs+ and Sr2+ ion exchange properties

This manuscript reports an environmentally benign method for the synthesis of Engelhard titanosilicate (ETS-4) using titanium isopropoxide or anatase as titanium source and citric acid as complexing agent. Slow release of Ti from the hydroxide or oxide precursors through the citric acid complex plays crucial role in formation of titanosilicate. Characterizations of the prepared material were carried out by powder X-ray diffraction (XRD), Scanning Electron Microscope – Energy Dispersive X-ray spectroscopy (SEM-EDS), Thermogravimetric – Differential Thermal Analysis (TG-DTA) and ion exchange studies. Caesium and strontium exchange capacities of the synthesised ETS-4 were found to be 220 mg/g and 76.2 mg/g, respectively. The saturation exchange equilibrium was attained within 60 min.

Effects of irradiation on interfacial strength and microstructure of double-layer mullite and alumina coating on SiC

Silicon carbide (SiC) ceramics hold great potential for use in nuclear-reactor components due to characteristics such as high-temperature strength and low activation. Despite their resistance against corrosion in harsh environments, they suffer elevated corrosion rates under particle irradiation. Thin anti-corrosion coatings, such as mullite bond layers and alumina top layers, are essential to enhance the irradiation stability of SiC. The objective of this study was to evaluate the irradiation stability of a double-layer coating developed to enhance the corrosion resistance of SiC in nuclear applications. The coating, which comprised a mullite bond layer and an alumina top layer, was applied to a SiC substrate using laser chemical vapor deposition. Irradiation experiments were conducted at 300 °C with 5.1-MeV Si ions up to 10 displacements per atom. To assess the interfacial strength, a novel testing method, called the double-notch shear compression testing method, was developed based on ASTM standards and was implemented using a nanoindenter. This approach enabled precise measurements of the mechanical integrity at the interfaces of the coating under irradiation. The results showed an increase in the interfacial strength at the SiC/mullite and alumina/mullite interfaces with irradiation. Microstructural analysis of the fracture surface through scanning electron microscopy–energy-dispersive X-ray spectroscopy revealed that cracks propagated within the mullite layer, indicating the presence of mullite on the fracture surface. Transmission electron microscopy (TEM) images indicated that a 2-µm-thick transition layer existed at the SiC/mullite interface but not at the alumina/mullite interface. The TEM–electron energy loss spectroscopy suggested that the Al-O bonding structures in the transition layer were changed from tetrahedral (AlO4) to octahedral (AlO6) through irradiation, and this structural transition may directly affect the strength.

Enhanced marmatite activation by copper with ammonium sulfate: An experimental and DFT investigation

The presence of iron atoms on the marmatite surface hinders effective interaction between the activator and the mineral, leading to unsatisfactory flotation performance through direct copper (Cu) activation. Hence, this study introduced ammonium sulfate to enhance the marmatite-activation capability by Cu ions. Additionally, the reinforcement mechanism was investigated through microflotation tests, atomic force microscopy (AFM), scanning electron microscopy-energy-dispersive X-ray spectroscopy (SEM-EDS), X-ray photoelectron spectroscopy (XPS), time-of-flight secondary ion mass spectrometry (ToF-SIMS), and density-functional theory (DFT) calculations. Microflotation results demonstrated that the addition of ammonium sulfate as a complexing reagent increased the flotation recovery of marmatite by 17.36%. AFM analysis revealed that marmatite subjected to enhanced activation (i.e., in the presence of ammonium sulfate) exhibited a considerably higher surface roughness than that subjected to direct Cu activation. Moreover, the average height of hill-shaped materials on the marmatite surface notably increased to 9.6 nm after enhanced Cu activation. SEM-EDS analysis revealed that the concentration of Cu atoms (2.2%) on the marmatite surface after enhanced Cu activation was nearly three times that (0.8%) after direct Cu activation. Additionally, XPS results indicated a considerably higher presence of the Cu–S component on the marmatite surface after enhanced Cu activation than after direct Cu activation. ToF-SIMS analysis indicated an increase in the fragment peaks of Cu+, CuOCS2+, OCS2−, and OC2H2S2− on the surface of enhanced-activated marmatite. Additionally, DFT calculations indicated that the presence of NH3 molecules enhanced electron transfer between Cu and S on the hydrated marmatite surface. The marmatite (1 1 0) surface exhibited more negative adsorption energy of Cu ions after the action of NH3 molecules, and NH3–Cu showed a more stable adsorption configuration than Cu. Therefore, the addition of ammonium sulfate enhanced the Cu activation for marmatite, thereby improving flotation performance.

Optimal Hydrofluoric Acid Etching Duration and Impact of Silane/Adhesive on Profilometric Properties and Bonding to Lithium Disilicate Glass Ceramics.

This study aimed to assess the surface roughness, surface free energy (SFE), and shear bond strength (SBS) on a lithium disilicate glass-ceramic surface following varying etching protocols (time variation) and application of silane either with or without adhesive material. Lithium disilicate glassceramic (LDGC) computer-aided design and computer-aided manufacture (CAD/CAM) blocks were cut using a slow-speed cutting mechanism. CAD/CAM blocks were then evaluated for surface roughness, 6 groups (n=20); SFE,12 groups (n=5); and SBS, 10 groups (n=10). The cut CAD/CAM blocks were randomly allocated to 28 groups. Groups were based on the following: 30 or 90 seconds of etching with 9% hydrofluoric acid (HF); application or absence of silane coupling agent (Sil); and application or absence of adhesive (Adh).The control group (Cont) had untreated surfaces. Unetched surfaces were surveyed with only silane (Sil), only adhesive (Adh), or silane+adhesive (SilAdh). Further etched groups were HF30 with HF for 30 seconds, HF30-Sil, HF30-Adh, and HF30-SilAdh. Alternative 90-second etching times produced similar groups: HF90, HF90-Sil, HF90-Adh, and HF90-SilAdh. A digital profilometer was used to assess the surface roughness of specimens, and two readings were recorded. Sessile drop analysis was used to examine SFE specimens, and the OWRK model was modified to measure liquid surface tension. A universal testing machine (UltraTester, Ultradent Products, Inc, South Jordan, UT, USA) was utilized for the SBS test, with the crosshead speed set at 0.5 mm/min until failure. Representative treated specimens from each group were submitted to surface morphological evaluation and chemical analysis using scanning electron microscopy/energy dispersive x-ray spectroscopy (SEM/EDXS) (n=3). After data collection, evaluation using one- or two-way analysis of variance and the post-hoc Tukey test (α=5%) was conducted. A longer etching time of 90 seconds produced a rougher surface. After the 90-second etching process, SFE displayed the greatest values; nevertheless, the use of silane did not affect SFE. For every group examined, the application of silane followed by adhesive resulted in an increase in SBS and more stable bonding over time. SEM/EDXS showed that etching times did affect the amount of cerium on the surface and altered surface morphology. Higher and more consistent bond strengths have been observed with longer etching periods. Silane and adhesive application on the ceramic surface showed stronger and enhanced bond strength, specifically when longer etching times were employed.

Electrokinetic in situ leaching of U from low-permeability uranium ore

In this study, the impacts of electrokinetic in situ leaching of uranium (EK-ISLU) on the pore structure and connectivity of the low-permeability uranium ore and its leaching efficiency were investigated. Our results demonstrated that a direct current field with an intensity of 7.5 V/cm increased the porosity by 7.07 % and enhanced the uranium leaching efficiency by 73.73 % using a sulfuric acid solution. Under electrical stimulation, the leaching agent exhibited uniform penetration ability through combined electromigration and electroosmosis effects, significantly improving the directed migration of the target ions. Various characterization techniques, such as Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy-energy dispersive X-ray spectrometry (SEM-EDS), three-dimensional computed tomography (CT) pore scanning and Brunauer-Emmett-Teller (BET), showed that the electrokinetic-induced action overcame the preferential flow phenomena, promoted the dissolution of the target minerals and gangue rocks, and notably improved the pore structure to ultimately enhance the uranium leaching efficiency. Our results provide valuable insights for the development of innovative technologies aimed at efficiently recovering U from low-permeability uranium ores.

Poly(ionic liquids-acrylic acid)-modified MIL-101(Cr) metal−organic frameworks: Preparation and efficient adsorption of europium☆

A novel composite material, Poly(IL-AA)@MIL-101(Cr), combining metal-organic framework, polymeric ionic liquid and acrylic acid, was synthesized for the selective and efficient adsorption of rare earths europium(III) (Eu3+). Characterization of the materials was carried out using techniques such as X-ray diffraction (XRD), Fourier transform infrared (FTIR), scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDS), thermogravimetric analysis (TGA) and Brunauer-Emmett-Teller (BET). The results demonstrate successful incorporation of the polymeric ionic liquid onto the material surface while preserving the crystal structure and morphology of MIL-101(Cr). Adsorption experiments were conducted to explore parameters including solution pH, initial Eu3+ concentration, and duration, with comprehensive analyses of adsorption kinetics, isotherms, and mechanisms. Findings reveal that Poly(IL1-AA)@MIL-101(Cr), Poly(IL3-AA)@MIL-101(Cr), and Poly(IL5-AA)@MIL-101(Cr) achieve adsorption equilibrium for Eu3+ at approximately 9 h with an equilibrium pH of 6.2. The adsorption of Eu3+ predominantly follows a pseudo-second-order kinetic model and Langmuir isotherm adsorption model. Moreover, the prepared composite material exhibits superior adsorption selectivity for Eu3+ over other metal ions in the mixture (K+, Mg2+, Ni2+, Co2+, Zn2+, La3+, and Nd3+). Even after five adsorption-desorption cycles, the composite material maintains satisfactory adsorption performance.

Enhancing CO2 Transport Across the PEG/PPG-Based Crosslinked Rubbery Polymer Membranes with a Sterically Bulky Carbazole-Based ROMP Comonomer.

A series of poly(ethylene glycol)-block-poly(propylene glycol) (PEG/PPG)- and 5,6-di(9H-carbazol-9-yl)isoindoline-1,3-dione (2CZPImide)-based crosslinked rubbery polymer membranes, denoted as PEG/PPG-2CZPImide (x:y), are prepared from the norbornene-functionalized PEG/PPG oligomer (NB-PEG/PPG-NB) and 2-(bicyclo[2.2.1]hept-5-en-2-ylmethyl)-5,6-di(9H-carbazol-9-yl)isoindoline-1,3-dione (2CZPImide-NB) via ring-opening metathesis polymerization (ROMP). The molar ratio (x:y) of the NB-PEG/PPG-NB (x) to 2CZPImide-NB (y) monomers is varied from 10:1 to 6:1. X-ray diffraction (XRD), scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDS), and pure gas permeability studies reveal that the comonomer 2CZPImide-NB successfully increases the d-spacing among the crystalline PEG/PPG segments, hence enhancing the diffusivity of gases through the membranes. The synthesized membranes exhibit good CO2 separation performance, with CO2 permeabilities ranging from 311.1 to 418.1 Barrer and CO2/N2 and CO2/CH4 selectivities of 39.4-52.0 and 13.4-16.0, respectively, approaching the 2008 Robeson upper bound. Moreover, PEG/PPG-2CZPImide (6:1), displaying optimal CO2 permeability and CO2/N2 and CO2/CH4 selectivities, shows long-term stability against physical aging and plasticization resistance up to 20 days and 10 atm, respectively.

Phase evolution and heavy metal solidification of cement desulphurized electrolytic manganese residue composite cementitious system under steam curing conditions based on thermodynamic simulation

The mechanical properties and microstructure of desulphurized electrolytic manganese (D-EMR) cement mortar under steam curing at 80 °C for 7 h and 7 days and standard curing for 3 days and 28 days were studied. The hydration products, microstructure and pore distribution were studied by Quantitative X-ray diffraction analysis (QXRD), scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDS), thermogravimetric-differential thermal analysis (TG-DTA) and backscattered electron (BSE). At the same time, the evolution of hydration products with age and the existence form of heavy metals under different curing conditions were simulated by GEMS thermodynamics. The results show that steam curing can promote the hydration reaction of cement and the secondary hydration of D-EMR. With the extension of steam curing time, the mechanical properties of the early stage are significantly improved. At a D-EMR content of 15 %, the compressive strength of D-EMR cement mortar after steam curing for 7 days is 1.15 times that of the control group under the same conditions, and the content of calcium hydroxide (CH) is 65.91 % of the control group. Steam curing can significantly improve the degree of C3S hydration of cement clinker and the secondary hydration of D-EMR, and increase the degree of polymerization of hydrated calcium silicate (C-S-H) gel. In addition, thermodynamic simulation showed that when the pH value was greater than 7.5, Mn2+ was mainly stable in the form of Mn(OH)2, MnOOH and Mn3O4, and there was no leaching risk. This will provide theoretical support for the use of D-EMR as a new type of supplementary cementitious material (SCM).

Pin-on-disc tribological characterization of single ingredients used in a brake pad friction material

Researchers have long been studying the effects of the modification of friction material compositions on their tribological properties. Predictive models have also been developed, but they are of limited use in the design of new compositions. Therefore, this research aims to investigate the tribological behaviour of single ingredients in friction materials to develop a tribological dataset. This dataset could then be used as a foundation for a cellular automaton (CA) predictive model, intended to be a tool for designing friction materials. Tribological samples were almost entirely composed of four distinct friction material ingredients, and one sample composed of their mixture was successfully produced. Pin-on-disc (PoD) tribometer testing and scanning electron microscopy/energy-dispersive X-ray spectroscopy (SEM/EDXS) analysis were used for the tribological characterization. Each material showed distinct tribological properties and evolution of the contact surface features, and the synergistic effect of their mutual interaction was also demonstrated by their mixture.

Polyoxometalate-Ionic Liquids for Mitigating the Effects of Iron Gall Ink Corrosion on Cellulosic Supports.

Iron gall ink (IGI), renowned for its indelibility, was the most important writing ink in the Western world from the 15th to the late 19th century. However, it is now known that IGIs induce acid-catalyzed hydrolysis and iron-catalyzed oxidation of the cellulose in historical paper documents. These mechanisms of deterioration cause significant damage to the writing support materials, including color alteration and burn-through appearance, and in the worst scenarios, physical disintegration of the supports. Minimally invasive, long-term effective conservation treatments that tackle the underlying mechanisms of IGI degradation and their corrosion effects are yet to be developed. This study introduces the deployment of hydrophobic and anticorrosive polyoxometalate-ionic liquids (POM-ILs) as colorless coatings to counteract IGI-corrosion of cellulosic supports. Model IGI-containing papers (mockups) were prepared, coated with POM-ILs, and artificially aged to assess the compatibility of POM-ILs with IGI-containing documents. Comprehensive monitoring using colorimetric and scanning electron microscopy-energy-dispersive X-ray spectroscopy (SEM/EDS) analyses showed minimal interference with the aesthetic properties and morphology of the IGI mockups. In addition, polyoxometalates (POMs) with vacant metal atom sites in the cluster shell can be used to coordinate free transition metal ions. The ability of a monolacunary Keggin-type polyoxotungstate to coordinate free Fe(II) from IGI solution was demonstrated using UV-vis analysis. This led to the formation of a dimeric species, [(SiW11O39Fe)2O]K12·28H2O, which was characterized by single-crystal X-ray diffraction. Altogether, this study points to POM-ILs as promising protective coatings for effectively preserving historical IGI-written heritage.

Determination of the significance of atomic concentration on surface properties of Ba x Mg1-x F2 alloy coatings via microscopic and spectroscopic techniques.

Both BaF2 and MgF2 compounds and Ba x Mg1-x F2 alloy thin films were deposited on glass and silicon (Si) substrates in nanometric sizes (100 ± 10 nm) in a high vacuum environment by radio frequency (rf) magnetron sputtering. Using BaF2 (99% purity) and MgF2 (99% purity) target materials and adjusting the power levels applied to these targets, Ba x Mg1-x F2 alloy coatings at different atomic concentrations were formed under the same vacuum conditions. The microstructure and surface characteristics of the samples were analysed with the help of spectroscopic and microscopic methods. For the surface characterization, with scanning acoustic microscopy (SAM), 2-dimensional surface acoustic images of the samples were mapped, the surface acoustic impedance values were determined, and information about the micro hardness of the materials was obtained. Surface roughness values and grain sizes were obtained by taking 3-dimensional surface images of investigated materials using atomic force microscopy (AFM). Average nanometric particle sizes were determined for each sample with scanning electron microscopy (SEM), therefore, information about surface homogeneity was obtained. For the microstructural characterization, quantitative elemental analysis was performed using scanning electron microscopy/energy dispersive X-ray spectroscopy (SEM-EDS), and stoichiometric ratios of atomic compositions were identified. By evaluating the data obtained from the microscopic and spectroscopic measurements, the effect of the atomic concentration parameter on the morphological properties of the material was determined. The usability of the produced binary fluoride alloy thin film coatings is promising for emerging optoelectronic, ceramic industry, biomedical and surface acoustic wave applications.

Gold Nanoparticle Mesoporous Carbon Composite as Catalyst for Hydrogen Evolution Reaction.

Increased environmental pollution and the shortage of the current fossil fuel energy supply has increased the demand for eco-friendly energy sources. Hydrogen energy has become a potential solution due to its availability and green combustion byproduct. Hydrogen feedstock materials like sodium borohydride (NaBH4) are promising sources of hydrogen; however, the rate at which the hydrogen is released during its reaction with water is slow and requires a stable catalyst. In this study, gold nanoparticles were deposited onto mesoporous carbon to form a nano-composite catalyst (AuNP-MCM), which was then characterized via transmission electron microscopy (TEM), powder X-ray diffraction (P-XRD), and scanning electron microscopy/energy dispersive X-ray spectroscopy (SEM/EDS). The composite's catalytic ability in a hydrogen evolution reaction was tested under varying conditions, including NaBH4 concentration, pH, and temperature, and it showed an activation of energy of 30.0 kJ mol-1. It was determined that the optimal reaction conditions include high NaBH4 concentrations, lower pH, and higher temperatures. This catalyst, with its stability and competitively low activation energy, makes it a promising material for hydrogen generation.

Preparation of high-purity magnetite from iron ore concentrate

In pursuit of environmental protection and green, low-carbon economic development, China has proposed the dual-carbon strategies of carbon peak and carbon neutrality. To achieve the dual-carbon goals, traditional steel metallurgical production processes are gradually shifting towards green and low-carbon hydrogen metallurgical processes. However, hydrogen metallurgical processes have strict requirements for raw materials and typically require the utilization of high-grade iron concentrates. The scarcity of high-grade iron ore in China severely constrains the development of hydrogen metallurgical processes. Therefore, this study proposes the utilization of ordinary magnetite concentrate to produce high-grade magnetite. Comprehensive analytical methods, including chemical analysis, X-ray fluorescence spectroscopy (XRF), X-ray diffraction (XRD) analysis, laser particle size testing, optical microscopy, scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDS), and mineral liberation analysis, were employed to elucidate the mineralogical characteristics of the iron concentrate. The analysis revealed that the iron concentrate had a total iron (TFe) grade of 65.56 %, with SiO2 and Al2O3 contents of 8.28 % and 0.38 %, respectively. Subsequently, a combined beneficiation process involving magnetic separation, flotation, and chemical leaching was conducted. Experimental results showed that a single magnetic separation obtained an iron concentrate grade of 67.52 % with an overall recovery of 86.18 %. Following magnetic separation, flotation was conducted to increase the concentrate grade. With one roughing and four cleaning flotation stages, a concentrate grade of 72.19 % and a 36.36 % overall recovery were achieved. A subsequent leaching operation after flotation yielded high-purity magnetite with a Fe grade of 72.30 % and an overall recovery of 35.68 %. The high-purity magnetite was confirmed to have a purity of up to 99.9 % based on chemical titration, XRD analysis, magnetic susceptibility measurement, and SEM analysis. Furthermore, detailed kinetics studies on leaching were conducted to elucidate the reaction mechanism, revealing an apparent activation energy of 25.70 kJ/mol. The successful implementation of this process will provide a benchmark for producing similar high-purity magnetite concentrates and contribute to China’s dual-carbon goals.

Characterization and Mechanism Elucidation of Nano-TiO2 Composites Prepared by Gaseous Detonation Method.

In this study, a series of nano-TiO2 composite materials, including nano-TiO2, nano-SnO2/TiO2, nano-SiO2/TiO2, and nano-Fe2O3/TiO2, were successfully synthesized via the gaseous detonation method. Comprehensive characterization of the synthesized samples was carried out through X-ray diffraction (XRD), transmission electron microscopy/high-resolution TEM (TEM/HRTEM), scanning electron microscopy/energy-dispersive X-ray spectroscopy (SEM/EDS), Brunauer-Emmett-Teller (BET) method, and Fourier transform infrared (FTIR) analysis, which unveiled the significant influence of precursor types on the microstructure of the composite materials. Specifically, the incorporation of Sn4+ promoted the transformation of TiO2 to the rutile phase, reducing particle sizes from 25 to 19 nm and increasing the specific surface area from 44 to 86 m2/g. In contrast, the introduction of SiO2 impeded the rutile phase formation, leading to a marked reduction in particle size to 14 nm and an enhancement of the specific surface area to 104 m2/g. Furthermore, the presence of Fe3+ promoted the formation of the rutile phase and enabled particle growth to 44 nm. These findings not only deepen the understanding of structural control in the synthesis of nano-TiO2 composite materials via the gaseous detonation method but also highlight the critical role of precursor selection in determining the properties of the resulting materials.