Scanning Electron Microscopy-energy Dispersive Spectroscopy Research Articles

Remineralising enamel caries with a novel peptide: An in vitro study

ObjectiveTo evaluate the antibacterial and remineralising effects of GAPI peptide on artificial enamel caries. MethodsHuman enamel blocks were exposed to Streptococcus mutans biofilm to create artificial carious lesions. The blocks were randomly assigned to either the GAPI treatment group or the deionised water control group, treated twice daily for 21 days. The viability, growth kinetics, and morphology of S. mutans biofilms were assessed using confocal laser scanning microscopy (CLSM), colony-forming unit (CFU) counting, and scanning electron microscopy (SEM). Lesion depth, mineral loss, calcium-to-phosphorus ratio, Knoop hardness, enamel surface morphology, and crystal characteristics of enamel lesions were determined using micro-computed tomography (Micro-CT), SEM-energy dispersive spectroscopy (EDS), a microhardness tester, SEM, and X-ray diffraction (XRD). ResultsCLSM showed that the dead-to-live ratio of S. mutans was 0.8±0.1 in the GAPI group and 0.4±0.1 in the control group (p<0.001). The Log CFUs were 6.9±0.7 in the GAPI group and 8.1±0.5 in the control group (p=0.002). SEM revealed confluent growth of S. mutans in the control group but not in the GAPI group, which also exhibited cell damage. Micro-CT showed that the lesion depth (µm) was 142±11 in the GAPI group and 178±20 in the control group (p<0.001), with mineral loss (gcm⁻³) of 1.1±0.1 and 1.5±0.1, respectively (p<0.001). SEM-EDS indicated that the calcium-to-phosphorus ratio was 1.71±0.02 in the GAPI group and 1.67±0.03 in the control group (p=0.006). Additionally, Knoop hardness was 302±22 in the GAPI group and 242±17 in the control group (p<0.001). SEM revealed an orderly pattern of enamel rods in the GAPI group, and XRD showed better crystallisation of hydroxyapatite in the GAPI group compared to the control group. ConclusionGAPI exhibits antibacterial and remineralising properties against artificial enamel caries. Clinical SignificanceIf the anti-caries properties of GAPI are confirmed in clinical studies, it could be used for caries prevention.

Study on the Effect of Dry and Wet Cycle Time Ratio on the Corrosion Behavior of 2198 Aluminum–Lithium Alloy

ABSTRACTThe corrosion of 2198 aluminum–lithium alloy in a marine atmospheric environment was simulated using a wet–dry alternating experimental setup. Weight‐loss measurement methods, electrochemical impedance spectroscopy (EIS), scanning electron microscopy/energy‐dispersive spectroscopy (SEM/EDS), macroscopic morphology testing, three‐dimensional morphology testing, and X‐ray photoelectron spectroscopy (XPS) were used to study the wet–dry alternating corrosion behaviors and mechanisms of 2198 aluminum–lithium alloys under simulated marine atmospheric environment. The results indicate that corrosion weight loss increases with decreasing wet‐to‐dry ratios, accompanied by an increase in the corrosion rate. Various data suggest that the primary corrosion products are composed of Al2O3, AlO(OH), and AlCl3. The reduction in the wet‐to‐dry ratio leads to the enrichment of Cl⁻ within the corrosion products, extending the contact time between the substrate and the medium, thereby intensifying the hydrolysis of Al³⁺. This exacerbates the dissolution at pitting sites, which in turn erodes and breaks down the corrosion product film, accelerating the overall corrosion process.

Evaluation of a novel activated carbon/graphene oxide as an efficient composite adsorbent for the removal of herbicide 2,4-Dichlorophenoxyacetic acid: Adsorption isotherm and kinetics study

Thysanolaena maxima-derived activated carbon/graphene oxide (TMAC/GO) composite was synthesized through a one-step mixing process via ultrasonication and used as an adsorbent for the removal of 2,4-Dichlorophenoxyacetic acid (2,4-D) herbicide from solution. Various analytical techniques, including Fourier-transform infrared spectroscopy (FTIR), Field emission scanning electron microscopy-energy dispersive X-ray spectroscopy (FESEM-EDX), X-ray diffractometer (XRD), Brunauer, Emmett, and Teller (BET) surface area analyzer, and Transmission electron microscopy (TEM) were employed to characterize the synthesized composite. Results showed that the TMAC/GO had a porous structure with a large surface area of 960 m2/g, an average pore diameter of 2.658 nm, and a total pore volume of 0.6372 cm3/g. A series of batch experiments were conducted for different adsorption parameters, which include TMAC/GO dosage (0.05–0.25 g/L), initial concentration (50–300 mg/L), pH (2–12), contact time (20–140 mins), and temperature (298–398 K). Adsorption thermodynamics, isotherm models, and kinetics were employed to understand the adsorption mechanism. The composite showed good adsorption ability with the Langmuir maximum adsorption capacity of 98.469 mg/g. When compared with TMAC, the composite exhibited higher removal efficiency under the same dosage, concentration, and temperature with variations in pH and time. The pseudo-second-order kinetics model justified the experimental results with an R2 value of 0.997. Furthermore, the composite displayed good reusability performance up to 5 cycles. These findings, along with the cost-effectiveness of the material and its selectivity towards the herbicide, suggest its practical importance for water decontamination.

Preparation of Purpurin-Fe2+ Complex Natural Dye and Its Printing Performance on Silk Fabrics.

In order to shorten the process of textile printing with natural dyes, develop new methods, and improve the color fastness and quality of printed products, this study presents a novel approach by synthesizing a natural complex dye through the interaction between purpurin and Fe2+ ions, resulting in a compound named purpurin-Fe2+ (P-Fe). This synthesized complex dye was meticulously characterized using state-of-the-art analytical techniques, including Fourier transform infrared spectroscopy (FT-IR), ultraviolet-visible (UV-Vis) spectrophotometry, and scanning electron microscopy energy-dispersive spectroscopy (EDS). The characterization confirmed the successful complexation of purpurin with Fe2+ ions. The prepared complex dye P-Fe was used for the printing of silk fabric. The optimized printing process involves steaming at a temperature of 100 °C for a duration of 20 min. In comparison to fabrics printed using direct dyes, the K/S values of the fabric printed with the P-Fe complex showed a significant enhancement, with all color fastness ratings achieving grade four. Furthermore, the proportion of metal elements on the white background of the printed fabric was found to be less than 0.180%, and the level of whiteness was above 50. The application of the P-Fe dye in silk fabric printing not only streamlines the printing process but also enhances the depth and speed of the printed color, effectively addressing the issue of color transfer onto a white background, which is commonly associated with natural dyes.

Mercury adsorption study and DFT calculations of sulfur-containing biomass composites prepared by inverse vulcanization

This study introduces an innovative and cost-effective biomass adsorbent, the sulfur/cardanol/potato starch composite (SCP), synthesized through inverse vulcanization for the remediation of mercury-contaminated waters. The SCP was characterized using Scanning Electron Microscopy/Energy Dispersive Spectroscopy (SEM/EDS), Fourier Transform Infrared Spectroscopy (FT-IR), Thermogravimetric Analysis (TGA) and X-ray Diffraction (XRD) to confirm its composition, morphology, and properties. The adsorption capacity of SCP for Hg(II) was 246.88 mg/g with a removal rate of 98.75 %. Adsorption kinetics followed a pseudo-second-order model, indicating chemisorption as the dominant mechanism, while adsorption isotherms were best described by the Langmuir model. Thermodynamic studies confirmed the adsorption process as spontaneous and endothermic. Density Functional Theory (DFT) calculations further elucidate the interaction mechanisms between mercury and the adsorbent, revealing that the thiyl radicals play a crucial role in the adsorption process. The SCP also exhibited a high selectivity for Hg(II) over other co-existing ions and maintains an adsorption capacity over 223.93 mg/g after five regeneration cycles, thus promising practical applications in environmental mercury management.

Analysis of the Impact and Mechanism of Polyacrylate-Based Composite Paste on the Performance of Recycled Aggregate.

This study developed three composite slurries for coating recycled aggregate by incorporating polyacrylate emulsion, fly ash, and gypsum into a cement-based mixture. The filling and pozzolanic effects of fly ash help to improve microcracks in the recycled aggregates. The polyacrylate emulsion forms a strong bonding layer between the cement matrix and the aggregates, enhancing the interfacial bond strength. Based on relevant studies, the following mix designs were developed: Slurry 1 consists of pure cement paste; Slurry 2 contains 15% fly ash and 3% gypsum added to the cement paste; Slurry 3 adds 22% polyacrylate emulsion to the slurry. The study first compared the effects of the three composite slurries on the crushing value and water absorption of recycled aggregates, and then analyzed their impact on the mechanical properties, permeability, and drying shrinkage of concrete. Finally, the mechanisms behind the enhancement were investigated using the Vickers Hardness Test (HV), Mercury Intrusion Porosimetry (MIP), and scanning electron microscopy-energy-dispersive spectroscopy (SEM-EDS). The results showed that the polyacrylate emulsion composite slurry had the most significant improvement effect. For recycled aggregate AL, the crushing value decreased from 28.8% to 22.5% and the saturated surface-dry water absorption decreased from 15.1% to 13.8% after cement slurry modification. After coating with the composite slurry, the crushing value further dropped to 18.2% and the water absorption to 9.5%. Two aspects of the performance of recycled aggregates are enhanced with the polymer composite slurry: first, fly ash provides nucleation sites for CH, reducing the tendency for directional CH alignment. Second, the long chains of PAE (polyacrylic ester) encapsulate cementitious particles, effectively filling surface defects on the recycled aggregates, improving the bonding strength at the new-to-old interface, and significantly enhancing the performance of both recycled aggregates and recycled concrete.

Influence of Accelerated Carbonation on the Performance of Recycled Concrete Containing Fly Ash, Recycled Coarse Aggregate, and Fine Aggregate.

In order to improve the quality of solid waste utilization, this study simultaneously used recycled coarse aggregate and recycled fine aggregate to prepare recycled aggregate concrete, with fly ash partially replacing cement as a binder. After the particle gradation of recycled aggregate was artificially adjusted into continuous gradation, the effects of accelerated carbonation on the performance and microstructure of recycled concrete were studied. The microstructural change was analyzed using mercury intrusion porosimetry and scanning electron microscopy-energy dispersive spectroscopy. Additionally, the environmental benefits of the recycled concrete were evaluated based on carbon emissions using the life cycle assessment method. The experimental results indicate that accelerated carbonation can increase the compressive strength of recycled concrete by up to 13%, and its microstructure becomes more compact after carbonation. The carbon emissions are reduced by more than 13% after using 20% fly ash, contributing to sustainable development. Additionally, the optimal replacement rate of recycled fine aggregate should be controlled to under 15% when both recycled coarse and fine aggregates are used.

Changes in physical and chemical properties of microplastics by ozonation

This study evaluated the altered properties of microplastics during the ozonation process in water matrices. The selected polymers include low-density polyethylene, high-density polyethylene, polypropylene, polystyrene, polyethylene terephthalate, and polyvinyl chloride. The morphology, contact angle, and chemical composition of the pristine and altered microplastics were characterized using field-emission scanning electron microscopy-energy dispersive spectrometry, contact angle analysis, Fourier-transform infrared spectroscopy, and X-ray photoelectron spectroscopy (XPS). Microplastic oxidation can lead to surface abrasion, cracking, and fragmentation. XPS analysis indicated that a CO double bond (carbonyl group) and carboxylic acid/ester bond (O−CO) were generated in the ozone process. In addition, all the carbonyl index values increased, implying that the number of oxygen functional groups on the surface of the microplastics increased. The contact angle also decreased, indicating that the hydrophilic portion of the microplastics increased due to oxidation. Microplastics, whose surfaces are roughened owing to oxidation or reduced in size owing to fragmentation, pose a fatal threat to aquatic life. In addition, microplastics with increased oxygen functional groups and hydrophilicity due to oxidation treatment have different adsorption properties. Relatively hydrophilic microplastics adsorb heavy metal cations that can adversely affect ecosystems by acting as heavy metal transport mediators.

A Cippus from Turris Libisonis: Evidence for the Use of Local Materials in Roman Painting on Stone in Northern Sardinia

The ancient Roman town of Turris Libisonis was located on the northern coast of Sardinia and was known in the past as an important naval port. Located in the Gulf of Asinara, it was a Roman colony from the 1st century BCE and became one of the richest towns on the island. Among the archaeological finds in the area, the cippus exhibited in the Antiquarium Turritano is of great interest for its well-preserved traces of polychromy. The artefact dates back to the early Imperial Age and could have had a funerary or votive function. The artefact was first examined using a portable and non-invasive protocol involving multi-band imaging (MBI), portable X-ray fluorescence (p-XRF), portable FT-IR in external reflectance mode (ER FT-IR) and Raman spectroscopy. After this initial examination, a few microfragments were collected and investigated by optical microscopy (OM), X-ray powder diffraction (XRPD), Fourier-transform infrared spectroscopy in ATR mode (ATR FT-IR) and micro-ATR mode (μATR FT-IR) and Scanning Electron Microscopy/Energy Dispersive Spectroscopy (SEM-EDS) to improve our knowledge and characterize the materials and to determine their provenience. The results contribute to a better understanding of the provenance of materials and shed light on pigments on stone and their use outside the Italian peninsula and, in particular, Roman Sardinia.

Beneficiation of High Sulfur Tertiary Coal of Assam with Burkholderia sp. GR 8-02. An Eco-Friendly Approach Toward Clean Coal Production

The high sulfur content in North-East Indian coal is one of the primary challenges with using it as an energy source. Therefore, the present study uses Burkholderia sp. GR 8-02 to explore coal beneficiation from the Tipong mine (T20 and T60) in Assam (North-East India). Various particle size fractions (−125 to +210 µm, −210 to +250 µm, −250 to +297 µm, −297 to +400 µm and −400 to +500 µm) were treated and subjected to petrographic and chemical analysis, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), Scanning Electron Microscope-Energy Dispersive Spectroscopy (SEM-EDS), Thermogravimetric analysis (TGA), and Raman spectral analysis. The results revealed a 39.04% and 32.43% reduction in total sulfur for T20 and T60 samples, respectively. The ash content decreased by 19.79% in the T20 coal sample and by 24.52% in the T60 coal samples, with a relative decrease in the mineral matter content of approximately 17.43%. Following beneficiation with Burkholderia sp. GR 8-02, the −125 to +250 µm coal fraction exhibited maximum ash removal. The T20 sample useful heating value increased from 8116 to 8203 kcal/kg and the T60 sample from 8060 to 8210 kcal/kg. X-ray diffraction and FTIR patterns showed mineral phases like quartz, kaolinite, and pyrite. The FTIR spectra indicated altered C-S, SO2, and C=O bonds. The thermal profile showed a 12.54% mass loss difference between untreated and treated coal samples, suggesting lower thermal stability post-treatment without affecting the useful heating value (UHV). The treated coal’s surface leaching and morphological structure changes were investigated using Scanning Electron Microscope-Energy Dispersive Spectroscopy (SEM-EDS) images. Raman analysis revealed increased carbon crystallinity and molecular structure in treated coal. This study offers an environmentally friendly and efficient approach to clean coal production.

Copper-Based Metal–Organic Framework: Synthesis, Characterization and Evaluation for the Hydrogenation of Furfural to Furfuryl Alcohol

AbstractA novel Cu-MOF was synthesized at room temperature from commercially available and inexpensive reagents. The pre-catalyst was characterized using X-ray photoelectron spectroscopy, high-resolution transmission electron microscopy, inductively coupled plasma-optical emission spectroscopy, Fourier transform-infrared spectroscopy, powder X-ray diffraction, Brunauer-Emmet-Teller (BET) and scanning electron microscopy-energy dispersive X-ray spectroscopy. The Cu-MOF was characterized as microporous material with BET surface area and pore volume of 7.47 m2/g and 0.27 cm3/g, respectively, and is stable in most solvents. The MOF was evaluated as a heterogeneous catalyst for the hydrogenation of furfural to furfuryl alcohol (FA). Cu-MOF exhibited a high conversion of FF (76%) with selectivity towards FA (100%) at 140 °C, 50 bar for 24 h. The MOF was reused four consecutive times with a loss in catalytic performance. The decrease in catalytic activity could be attributed to the formation of inactive Cu(0) as revealed by HR-TEM and XPS studies. The HR-TEM of spent Cu-MOF showed a uniform particle size diameter of 3.5 nm. This work is significant in providing new strategies for the design and fabrication of highly selective MOF catalysts for the FF upgrading.

Green synthesis of copper oxide nanoparticles using solanum melongena seeds extract and its applications in degradation of Rose Bengal dye, antibacterial, catalytic reduction and antioxidant activity

The generation of copper oxide (CuO) nanoparticles using a biogenic extract (solanum melongena seeds) was the primary focus of this study. As prepared catalyst has been utilized for dye degradation of Rose Bengal and studies on Antibacterial and Antioxidants. The catalyst was characterized for its structural aspects by using Scanning electron microscopy - energy dispersive spectroscopy (SEM-EDS), Powder X-ray Diffraction (PXRD), Fourier Transform - InfraRed spectroscopy (FT-IR), Thermogravimetric Analysis (TGA), Brunauer-Emmett-Teller (BET) and UV–Visible DRS. The characterization results of XRD shows that the catalyst is in monoclinic phase. Copper Oxide is irregular in morphology and the average particle size is 47.97 nm which can be obtained using the SEM images and EDS spectra shows the Oxygen and Copper atoms presence which indicates the free from impurities of the fabricated biogenic CuO nanoparticles. FT-IR result indicated the stretching frequency of Cu–O appears at 487 cm−1. TGA data reveal that high-purity and thermally stable nanoparticles were fabricated, by the absence of significant weight losses at temperatures greater than 400 °C. Through UV–Visible DRS the calculate band gap was found to be 2.8eV. Based on the characterisation results the best catalyst was used to degrade the Rose Bengal dye within 60 min and also carried out the antibacterial and antioxidant activity which was found to be satisfactory when compared with their standard values.

Development and characterization of nitazoxanide-loaded poly(ε-caprolactone) membrane for GTR/GBR applications

ObjectiveGuided tissue/guided bone regeneration (GTR/GBR) membranes are widely used for periodontal bone regeneration, but their success depends on a bacteria-free environment. Systemic antibiotic treatment often proves inadequate, moreover, the increasing prevalence of antibiotic resistance in oral infections exacerbates this challenge. This study aimed to fabricate antibacterial membranes using a new class of antibiotics for local drug delivery, to eradicate infections and promote tissue regeneration. MethodsMembranes loaded with nitazoxanide (NTZ) were fabricated via electrospinning using poly(ε-caprolactone) (PCL) with varying concentrations of NTZ (0 %, 2.5 %, and 5 % w/w) relative to the polymer weight. Morphochemical of NTZ-loaded membranes were assessed using scanning electron microscopy-energy dispersive spectroscopy (SEM-EDS) and Fourier Transform Infrared spectroscopy (FTIR). Mechanical properties were evaluated using universal testing machine and NTZ release profile from membranes was determined by spectrophotometer (λmax = 444) for 14 days. Antimicrobial efficacy against periodontal pathogens, cell compatibility and mineralization were evaluated using periodontal ligament stem cells (PDLSCs). ResultsOptimized spinning parameter maintained a uniform fiber diameter and successful loading of NTZ was confirmed by SEM-EDS and FTIR. NTZ incorporation did not significantly affect mechanical properties, whereas the drug release kinetics showed an initial burst, followed by sustained release over 14 days. NTZ-loaded membranes demonstrated antibacterial activity against Aggregatibacter actinomycetemcomitans (Aa) and Fusobacterium nucleatum (Fn). Importantly, the presence of NTZ showed minimal cell toxicity; however, it reduced the mineralization potential compared with that of the pure PCL membrane, which increased over time. SignificanceTaken together, these findings established that NTZ-loaded membranes could be promising barrier membrane to counteract microbial environment and aid periodontal bone regeneration.

Geochemical characterization and reserve estimation of the economic heavy minerals of Sonadia Island, Bangladesh

The goal of the current study is to understand the elemental concentration, reserve assessment, mineralogical composition, and distribution of heavy minerals in the dune sands, foreshore, and backshore of Sonadia Island, Southeast Bangladesh. The study area yielded a number of drill hole composite sand samples that were used for density and magnetic separation of heavy minerals. These samples were then subjected to petrographic characterization, grain counting, mineralogical analyses using scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM–EDX), x-ray diffraction (XRD), and bulk sand geochemistry using X-ray fluorescence (XRF). The results of heavy liquid separation show that the total heavy mineral (THM) enrichments in foreshore sand (about 4.86%), backshore sand (about 9.03%), and dune sand (about 22.28%) are significantly higher. After characterizing the sand samples from Sonadia Island based on the abundance of each mineral species, the average content values relative to total economic heavy minerals (TEHM) were determined to be 38.14% ilmenite, 5.74% magnetite, 51.52% garnet, 1.01% zircon, 3.57% rutile, and 0.01% monazite. An SEM–EDX examination reveals that the elemental concentration of ZrO2 in zircon is 66.60%, while the average TiO2 content in rutile is ~ 95%, whereas TiO2 is 45% and the total Fe2O3 is 45.70% in ilmenite. Major phases including amphibole (tremolite) 45.9%, muscovite 15.6%, quartz 12.6%, garnet (almandine) 10.9%, dolomite 7.9%, ilmenite 4.1%, and kaolinite 1.3% are also identified by the XRD pattern. There are an estimated 19,794 tons of garnet in the foreshore sand, 47,324 tons in the backshore sand, and 276,868 tons in the dune sand within the reserve, making it the most prevalent heavy mineral. Ilmenite is the second most common heavy mineral, with quantities detected in the foreshore (15,016 tons), backshore (30,487 tons), and dune sand (215,092 tons).

Chemical composition, mutagenicity, and cytotoxicity of urban submicron particulate matter (PM1) in Agra, India

This study, conducted in Agra, India, examined the mass concentrations, chemical compositions, and seasonal variations of submicron particles (PM1). The concentrations of metals, water-soluble inorganic ions (WSIs) including anions (F−, Cl−, NO₃−, SO₄2−) and cations (Ca2+, K+, Mg2+, NH₄+, Na+), organic carbon (OC) and elemental carbon (EC) and polycyclic aromatic hydrocarbons (PAHs) in PM1 extract were determined using Inductively Coupled Plasma-Optical Emission Spectroscopy (ICP-OES), Ion Chromatography, Thermogravimetric Analysis and Gas Chromatography-Mass Spectrometry (GC–MS) respectively. For morphological observation of PM1 particles, Field Emission Scanning Electron Microscopy-Energy Dispersive X-ray spectrometry (FESEM-EDS) was used. The annual average concentration of PM1 was 82.9 ± 33.4 μg/m3, which exceeds the World Health Organisation's (WHO) safe limit for PM2.5 of 5 μg/m3 by a factor of 17. The PM1 mass composition included metals (31 %), WSIs (28 %), OC and EC (9.8 %), and PAHs (0.4 %). Winter recorded the highest PM1 concentration (96.1 ± 25.8 μg/m3), followed by post-monsoon, summer, and monsoon seasons. The average concentration of PAHs was 364.6 ± 226.6 ng/m3. Positive Matrix Factorization (PMF) identified traffic, emissions from biomass/coal and wood combustion, industrial/stationary sources, and secondary aerosols as potential contributors. The Ames test revealed the presence of frameshift mutations and base pair substitutions, especially in winter and post-monsoon. Additionally, PM1 exhibited cytotoxic effects on V-79 cells, with heightened toxicity during winter and prolonged exposure in other seasons. This study underscores the urgent need to address local emission sources and establish regulatory standards for PM1 in urban areas.

Efficient dye removal using manganese oxide-modified nanocellulosic films from sugarcane bagasse

Removing toxic dyes from industrial wastewater is crucial for environmental protection. This research introduced novel composite films of manganese oxide (MnO2)-modified nanocellulose (MCel) and unmodified nanocellulose (Cel) derived from sugarcane bagasse for dye removal. Nanocellulose was extracted from sugarcane bagasse and subsequently transformed into MCel through in-situ MnO2 synthesis. The MCel/Cel composites, with various MCel to Cel ratios, were fabricated into films and evaluated for their efficiency in removing methylene blue (MB). The films were characterized using Fourier transform infrared spectroscopy for functional group analysis, X-ray diffraction for crystallinity, X-ray photoelectron spectroscopy for chemical state analysis, field emission scanning electron microscopy-energy dispersive spectroscopy for morphology and elemental composition, and Thermogravimetric Analysis for thermal behaviors. Adsorption results showed that all MCel/Cel composite films achieved over 97 % removal of MB (initial concentration 100 mg L−1) within 24 h, with convenient adsorbent retrieval after adsorption. The adsorption process followed a pseudo-second order kinetic model and Langmuir adsorption isotherm. The optimal 95:5 MCel/Cel film exhibited a rate constant of 6.16 × 10−4 g mg−1 min−1 and the calculated adsorption capacity of 181.85 mg g−1. These results demonstrate significant potential for wastewater treatment and sustainable waste valorization by converting sugarcane bagasse cellulose into environmentally friendly adsorbents for contaminant removal.

Late Holocene geochemical signature of inter reef mixed sediments on the northeastern Brazilian outer shelf

The northeastern outer shelf in Brazil is a complex ecotone that holds significant information on Holocene sedimentary processes and evolution. X-ray diffraction (XRD), X-ray fluorescence (XRF), and scanning electron microscopy/energy dispersive spectrometry (SEM/EDS) were employed to investigate bioclastic sedimentary facies and patches of relict siliciclastic sands. Radiocarbon dating (AMS) indicates that the carbonate sediments and corals formed in the past millennium. The sediment samples were divided into two groups using a multivariate analysis of XRD and XRF. The first group consists of siliciclastic materials, characterized by Si, Al, Fe, K, Zr, and Ti, and has low levels of carbonate and organic matter. The second, bioclastic and mixed facies, has a high carbonate content and exhibits elevated concentrations of Ca, Sr, and Mg, indicating authigenic processes. The EDS data revealed that the shells predominantly consisted of Cl, Cu, Al, Fe, and Ca. The terrigenous sites are detached from the coastal sources and are mainly located within the reef areas of the outer shelf. The erosion processes in these areas were inefficient to eliminate the siliciclastic sediments. This deposit trapped in inter reef sediments holds the key to understanding the timing and interactions between past coastal processes, shelf valley incision, and reef evolution during the Late Holocene transgression.

Research on the Corrosion Resistance of Electrodeposited Ni-SiC Composites Constructed for Steel Storage Tank Application.

In this paper, the effects of the SiC phase incorporated in Ni substrate deposits on storage tank steel during electrodeposition at different current densities are explored. The microstructure, phase content, and corrosion resistance of the resulting Ni-SiC composites were investigated by scanning electron microscopy (SEM) matched with energy disperse spectroscopy (EDS), X-ray diffraction (XRD), and an electrochemical workstation, respectively. SEM micrographs and EDS results show that at 2.5 A/dm2, the composites presented a smooth and compact structure with high SiC content, while at 1.8 or 3.2 A/dm2, it became uneven and loose in structure with low SiC content. XRD patterns showed that the nickel grain size of composites firstly increased and then decreased with the growth of the current density. Notably, the Ni-SiC composite produced at 2.5 A/dm2 possessed a higher corrosion potential (-0.507 V) and lower corrosion current density (2.439 μA/cm2), illustrating that its excellent anti-corrosion ability was superior than that of other two composites. Hence, SiC co-deposited at 2.5 A/dm2 conducted as a protective barrier and inhibited the corrosion rate against a corrosion medium of Cl- and SO42- ions. In addition, the corrosion relationship illustrated that the SiC content of Ni-SiC composite firstly increased and then decreased with the growth of the current density, while the corrosion weight loss of Ni-SiC composites firstly decreased and then increased.

Construction of MIL-100(Fe)-DMA material for efficient adsorption of Sr and Cs ions from radioactive wastewater

A novel metal-organic framework (MOF) material, MIL-100(Fe)-DMA, was synthesized using the solvothermal method. The structure of the MOF was characterized using scanning electron microscopy-energy dispersive X-ray spectroscopy, N2 adsorption–desorption isotherms, X-ray diffraction analysis, Fourier-transform infrared spectroscopy, X-ray photoelectron spectroscopy, and Mössbauer spectroscopy. Batch adsorption experiments were performed to investigate the effects of initial Sr2+ and Cs+ concentrations, adsorption time, pH, and coexisting cations on the adsorption performance of the material. The adsorption mechanism was further elucidated using adsorption kinetics and isotherm models. The results indicated that the adsorption of Sr2+ and Cs+ does not significantly affect the MOF material structure. As reaction time and initial ion concentration increased, the adsorption capacity of MIL-100(Fe)-DMA for Sr2+ and Cs+ increased rapidly and then gradually reached equilibrium. Optimal adsorption occurred under alkaline conditions, with maximum adsorption capacity observed at pH = 8. The adsorption process for Sr2+ and Cs+ was well described by the pseudo-second-order kinetic model, the Weber–Morris model, and the Langmuir adsorption isothermal model. The adsorption process was mainly identified as monolayer chemical adsorption, influenced by multiple factors. Characterization combined with density functional theory calculations revealed that the unsaturated carboxylic acid groups on the surface of the MOFs play a crucial role in the interaction with Sr2+ and Cs+.

Investigation of tool traverse speed on surface integrity of nano composites processed by friction stir process

This work examines the effects of different tool traverse speeds on the surface integrity of AA7075 reinforced with graphene oxide (GO), silicon carbide (SiC) and graphene nanoplatelets (GNPs) nanoparticles during Friction Stir Processing (FSP). Three different traverse speeds of 20, 25 and 30 mm/min, respectively, were used for FSP operations. The resulting nanocomposites were thoroughly analysed using methods including optical microscopy, tensile testing, fracture morphology analysis, microhardness testing, X-ray Diffraction (XRD), Field Emission Scanning Electron Microscopy-Energy Dispersive X-ray Spectroscopy (FESEM-EDAX) and non-contact surface interferometry. The results show that the creation of a refined microstructure with equiaxed grains was aided by tool traverse speeds between 20 and 25 mm/min. Notably, an Ultimate Tensile Strength (UTS) of 358 MPa, microhardness of 139 HV, refined crystalline size of 47.162 nm and average roughness (Ra) of 1.53 μm were obtained with the AA7075+SiC nanocomposite under tool traverse speed of 25 mm/min. On the contrary, surface layer defects developed at a traversal speed of 30 mm/min. Through the use of mechanical stirring and severe plastic deformation (SPD), this study aids in changing the microstructure of the airplane frames.