Scanning Electron Microscopy-energy Dispersive X-ray Research Articles

Organosilane Modification of Lignin and Lignosulfonate: Structure and Compatibility in PVDF Membrane

The high difference in surface tension between the filler and the polymer often constrains membrane compatibility. To reduce the surface tension, organosilane such as GPTMS is usually used to improve miscibility. In this study, GPTMS was introduced to produce lignin-GPTMS (LG) and lignosulfonate-GPTMS (LsG). The modification was done by reacting lignin and lignosulfonate with GPTMS using ethanol as the media. The product was characterized using Fourier Transform InfraRed (FTIR), X-ray Diffraction (XRD), Particle Size Analyzer (PSA), Scanning Electron Microscope-Energy Dispersive X-ray (SEM-EDX) and microscope. The success of functionalization was shown in FTIR spectra with the vibration of Si-O at 1034 cm-1 and 528 cm-1. The XRD analysis presents that the filler material has an amorph and crystalline structure. The functionalization using a 2:1 ratio increases zeta potential absolute and particle size due to the silane being a bridge and making a larger macromolecule. For a ratio of 1:1, a higher organosilane compound results in breaking siloxane linkages and making smaller molecules. Mixed LG and LsG into PVDF membrane conducted to analyze filler compatibility. The sulfonation and functionalization of GPTMS increase the compatibility of lignin in PVDF membrane with the best homogeneity achieved by a membrane with the addition of LsG 1:1.

Exploring the Potential of Recycled Polyethylene Terephthalate—Lignocellulose/Carbon Nanotube–Graphene Nanosheets an Efficient Extractor for Oil Spill

The global challenge of oil spill treatment has been addressed using nanocomposite-based natural fibers. These materials offer great potential in oil spill cleanup and are considered due to their environmental friendliness, high efficiency, and low cost. Thus, the current study reports a novel composite fabricated from date palm fiber (DPF) and recycled polyethylene terephthalate (rPET) with a proper combination of a mixture of carbon nanotubes (CNTs) and graphene nanosheets (GNSs) for oil removal. The established nanocomposite (DPF-rPET/CNT/GNS) was fabricated via physical mixing of various quantities (0.9, 0.8, and 0.7 g) of PET, along with varying loads of DPF at different proportions of CNT:GNS. The prepared nanocomposite (DPF-rPET/CNT/GNS) was fully characterized using scanning electron microscopy–energy dispersive X-ray (SEM-EDX) analysis, transmission electron microscopy (TEM), thermogravimetric analysis (TGA), Fourier-transform infrared spectroscopy (FTIR), and Brunauer–Emmett–Teller (BET) analysis. In static experiments and under the optimal parameters of pH, sorbent doze, shaking time, and quantity of diesel oil), the established sorbent (DPF-rPET/CNT-GNS nanocomposite) displayed excellent adsorption capacity (98 mg/g). This study also expands the utility of the sorbent for the reusability of the oil adsorption, maintaining performance after five cycles. The adsorption data fitted well with the Langmuir isotherm model with a correlation coefficient (R2) of 0.99 and maximum adsorption capacity of 99.7 mg/g, indicating monolayer adsorption. Additionally, the adsorption kinetics followed a pseudo-second-order model, with an R2 near unity and an adsorption capacity of 99.09 mg/g. This study highlights the promising potential of the DPF-rPET/CNT-GNS composite as an effective adsorbent for treating oily water.

Preliminary Assessment of Morphology and Elemental Composition of Fine Particulates in Selected Urban Areas of Java Island

Rapid urbanization and high population density in three major cities in Indonesia, Bandung, Jakarta, and Tangerang have led to significant air quality issues. Fine inhalable particles (PM2.5) with distinct morphologies and elemental compositions pose considerable health risks. This study evaluates the morphology and chemical composition of PM2.5 in these urban areas on Java Island. PM2.5 samples were collected for 24-hour periods using a Teflon filter with the Super Speciation-Air Sampling System (SuperSASS) following the EPA sampling schedule, from May to September 2022. The Teflon sample with the highest PM2.5 concentration, representative of both weekdays and weekends, was selected for morphological analysis using Scanning Electron Microscopy-Energy Dispersive X-ray (SEM-EDX) and elemental characterization using Energy-Dispersive X-ray Fluorescence (ED-XRF) Epsilon. SEM images revealed distinct morphological characteristics at each site. In Bandung, particles were irregularly shaped, agglomerated, and flaky, with sizes ranging from 1.1-1.6 µm on weekdays and 0.9-1.3 µm on weekends. Jakarta has particles with semi-crystalline, tabular, elongated, and puff-like morphology, with sizes predominantly from 0.5-0.8 µm on weekdays and 0.9-1.3 µm weekends. In Tangerang, particles were irregularly faceted and agglomerated, with sizes between 0.5-1.3 µm on weekdays and 0.9-1.4 µm on weekends. Teflon-derived minerals (C,F) were present across all sites. EDX spectra revealed Ca-rich particles in Bandung, while S-rich particles were observed in Jakarta and Tangerang. XRF analysis further proved the major and minor elements, reflecting local pollution sources. The combined use of SEM-EDX and XRF offers a comprehensive profile of PM2.5, highlighting specific pollution sources in each city.

Mechanical Properties and Microstructure of Alkali-Activated Cements with Granulated Blast Furnace Slag, Fly Ash and Desert Sand

In this study, desert sand was used as supplementary materials in alkali-activated cements (AAC) with granulated blast furnace slag (GBFS) and fly ash (FA). For the first time, a systematic investigation was conducted on the effects of various treatment methods and contents of desert sand on the strength and microstructure of AAC. This study also analyzed the X-ray diffractometer (XRD), Scanning Electron Microscopy-Energy Dispersive X-ray Microanalysis (SEM-EDX), Mercury Intrusion Porosimetry (MIP), pH values, and Fourier-transform infrared spectroscopy (FT-IR) properties of AAC pastes containing differently treated desert sand to uncover the mechanisms by which these treatments and dosages influence mechanical properties of AAC. Untreated desert sand (DS), temperature-treated desert sand (DS-T), and ground desert sand for two different durations (20 mins and 30 mins) all exhibited some pozzolanic activity but primarily acted as fillers in the AAC pastes. Among the samples, DS-T demonstrated the highest pozzolanic activity, though it was still less than that of fly ash (FA). The optimal dosage for the modified desert sands was determined to be 10%. However, The optimal dosage of different modified desert sands is 10%. The flexural strength of DS-G30-10 reaches 6.62 MPa and the compressive strength reaches 72.3 MPa, showing the best comprehensive mechanical properties.

Enhancing Sustainable Production of Biodiesel from Xanthoceras sorbifolia Bunge Oil Using Bio-Based Heterogeneous Catalyst

The swift exhaustion of natural oil reserves and worsening environmental issues have prompted the quest for an economical method to produce biofuels. The superiority of heterogeneous catalysis promotes the development of bio-based catalysts. Carbon materials prepared from agricultural and forestry biomass waste have good application prospects in catalysis. In the present study, Xanthoceras sorbifolia shell waste was used as the raw material, Xanthoceras sorbifolia Bunge Carbon (XC) was used as the catalyst carrier, and K2CO3 was used as the activator to prepare a heterogeneous catalyst (KXC). The heterogeneous catalyst was characterized by scanning electron microscopy-energy dispersion X-ray spectroscopy (SEM-EDS), Fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), X-ray diffraction (XRD), and Brunauer–Emmett–Teller (BET) and X-ray photoelectron spectroscopy (XPS) analysis techniques to evaluate its chemical composition, structure, and physical morphology. EDS and XPS revealed the presence of K metal, which provided an alkaline site for the transesterification reaction to produce biodiesel. The biodiesel yield was observed by gas chromatography−mass spectrometry (GCMS). Under the reaction conditions of a methanol-to-oil molar ratio of 12:1, a reaction time of 90 min, a temperature of 65 °C, and a catalyst loading of 4 wt.% using 25KXC-600-4, the yield of biodiesel can reach 95.13 ± 0.82%. After being repeated five times, the yield was still 58.11 ± 3.80%. The catalyst has no waste generation, and has the characteristics of simple preparation and environmental friendliness, which make it a green heterogeneous catalyst for biodiesel production.

Durability properties of ambient-cured fly ash-phosphogypsum blended geopolymer mortar in terms of water absorption, porosity, and sulfate resistance

This paper aimed to investigate the durability of ambient-cured fly ash-phosphogypsum blended geopolymer mortar (GPM) when exposed to a water and sulfate environment at different durations. Water absorption, porosity, and sulfate resistance tests were conducted to determine the durability. The GPM was prepared at 0 wt%, 30 wt%, and 40 wt% PG replacement of fly ash content in the mixture. The mix proportions were determined experimentally at 10 M sodium hydroxide, alkaline liquid/precursor of 0.4, sodium silicate/sodium hydroxide of 1.5, and binder/aggregate of 1.0. The samples were immersed in potable water and magnesium sulfate solution. The changes in weight, length, and compressive strength were monitored. Scanning electron microscopy-energy dispersive X-ray spectroscopy was used to analyze the structure and composition. The findings showed that GPM with 30 wt% phosphogypsum added had lower water absorption, porosity, and sulfate attack than GPM with 0 wt% phosphogypsum attributed to the formation of hydrated gels leading to a dense microstructure and improved strength. The changes in weight, length, and strength variations trend for GPM were within optimal performance standards. This has implications for the practical application of GPM in construction where it can be used as an alternative to Portland cement mortar in sulfate-rich environments.

Mitigation effect of a biodegradable surfactant N,N,N-trimethyl-2-(((hexadecyloxy)carbonyl)oxy)ethan-1-aminiumiodide for mild steel corrosion in 5% HCl: Experimental and theoretical insights

A cleavable cationic surfactant having carbonate linkage, N,N,N-trimethyl-2-(((hexadecyloxy)carbonyl)oxy)ethan-1-aminiumiodide referred to as THC was synthesised and characterized employing elemental analysis, FT-IR (Fourier Transform Infrared Spectroscopy), 1H NMR (Nuclear Magnetic Resonance) and 13C NMR. The extent of corrosion inhibition of THC was for the first time studied experimentally and theoretically on mild steel (MS) substrate in 5 % HCl solution at temperatures 303, 313, 323, 333, 343, 353 K. Experimental investigations include gravimetric analysis, potentiodynamic polarization (PDP) and electrochemical impedance analysis (EIS). THC provided maximum inhibition efficiency of 93.2 % at concentration of 1×10−4 M at 303 K which was further raised to 98.1 % at 353 K. PDP studies reveal that given surfactant is mixed type inhibitor. Surface studies such as contact angle measurement, AFM (Atomic Force Microscopy), SEM-EDX (Scanning Electron Microscope-Energy Dispersive X-ray Analysis), and XPS (X-ray Photoelectron Spectroscopy) were employed to justify the adsorption of inhibitor molecules on MS surface. Furthermore, biodegradability test on THC was done to support the environment friendly nature of the surfactant.

Characterization of chemical properties of fish-flavoured spicy tamarind cube

Fish-flavoured spicy tamarind cube is categorized as a type of bouillon cube. It is a processed food that has been developed and benefits the consumers due to low cost, being ready to use, reduced cooking time and giving intense flavour to the cooking dish. Food processing improves the stability, safety, taste and makes the food healthier. While there are various advantages to processing, the chemical food characteristics might be adversely affected. The study aimed to evaluate the amount of chemical composition, macromolecule, phytochemical content, peroxide value and antioxidant activity present in the fish-flavoured spicy tamarind cube. The analysis was performed using a different methodology. The content of mineral and ascorbic acid of the cube was evaluated by using scanning electron microscopy-energy dispersive X-ray (SEM-EDX) and titration methods respectively. Carbohydrate was estimated by difference using equation and protein by micro Kjeldahl method. For both phytochemical compounds, total phenolic and flavonoid are measured spectrophotometrically in this study. In addition, peroxide value was determined by titration method and antioxidant activity was assayed using 2,2- diphenyl-1-picrylhydrazyl (DPPH) free radical. The result showed the cube contained 2.12% sodium, 1.22% copper and 0.43% potassium while the ascorbic acid value was 66.00 mg/100 g. The macromolecule content recorded was 40.15 g/100 g for carbohydrates and 7.54 g/100 g for protein. The cube had 10.77 mg GAE/g and 21.72 mg QE/g for total phenolic and flavonoid respectively. The peroxide value of the cube was 9.52 meq/kg and classified in a moderate oxidation state. Furthermore, the half-maximal inhibitory concentration (IC50) for antioxidant activity analysed was 89.04 µg/mL which means the cube shows intermediate antioxidant activity. Based on the result, the cube is safe to consume and can provide health benefits to consumers.

Effect of traps and conductive pathways on electron emission from copper broad-area composite emitters

This study investigates electron emission from copper broad-area emitters (CBAEs) and copper broad-area composite emitters (CBACEs) based on the principles of trapping and conductive pathways. Emission current measurements were conducted on two CBACEs, which consisted of copper coated with a 300–400 μm epoxy resin and subjected to high voltages up to 15 kV. The research specifically examines the ‘switch-on’ and collapse phenomena occurring within the epoxy layer. Field emission microscopy (FEM) was utilized in a high-vacuum environment ( 10−6 mbar) to observe these effects. A comprehensive model is developed to explain the formation of conductive pathways within the epoxy layer, allowing electrons transfer from traps to the surface. This model treats the composite emitter as a trap-rich capacitor. The study also clarifies the effects of trap density and epoxy layer thickness on the collapse process. To gain a deeper understanding of the model, changes in the I-V curve were examined. Simulations, scanning electron microscopy-energy dispersive x-ray spectroscopy (SEM-EDX) images, and Fourier transform infrared spectroscopy (FTIR) analysis were employed to understand the collapse mechanism of the epoxy collapse. Additionally, Nyquist and Cole–Cole plots were analyzed across frequencies ranging from 1 to 106 Hz before and after applying a high electric field on the samples, revealing changes in the capacitive component and the role of diodes in the formation of conductive channels.

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.

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.

Investigation of The Stability of The Lysozyme in Magnetic Particles for Drug Delivery

This research investigated lysozyme stability in the presence of magnetic particles for drug delivery. Lysozyme can mostly be found in the hen egg albumin, and it also acts as an essential agent, which is antibodies to fight harmful bacteria or shield the human body. The problems in this research are magnetic particles that can cause toxicity and reduce the therapy's efficiency due to the degradation of carriers (drugs). To minimise this problem, the stability and activity of the lysozyme and Fe2O3 were investigated. The structure of lysozyme and Fe2O3 before and after adding acid or alkaline was defined, and the suitability of Fe2O3 as a drug delivery was determined. The stability of the lysozyme and Fe2O3was identified using an Ultraviolet-Visible (UV-Vis) Spectrophotometer, and the structure was investigated using a Field Emission Scanning Electron Microscope (FESEM) and Scanning Electron Microscope- Energy Dispersive X-Ray (SEM-EDX). Different concentrations become the parameters of this research as a comparison between the samples. This research found that the combination of the lysozyme alkaline material was suitable for the body at a pH of 12.2. It also found that Fe2O3 is ideal for drug delivery in the body when the lysozyme can be carried by Fe2O3 and dissolved in the Fe2O3.

Electrochemical recovery of ruthenium via carbon black nano-impacts

The recovery of ruthenium from low-concentration solutions poses a significant challenge due to its scarcity and rising economic value, and nano-impact electrochemistry has emerged as a promising method for efficient recovery of critical metals from solution through deposition during impacts of non-metallic nanoparticles. In this study, we investigate the redox chemistry of ruthenium on carbon black via the impact technique and demonstrate the ability to recover ruthenium from solution. The reduction (electrodeposition) and oxidation of Ru3+ ions in solution onto carbon black nanoparticles can be observed during nano-impacts with the respective onset potentials of these redox processes agreeing with those obtained from solution voltammetry. Upscaled experiments focusing on the electroreduction process, led to the formation of RuOx deposits, confirmed through scanning electron microscopy/energy-dispersive X-ray (SEM/EDX) analysis, X-ray photoelectron spectroscopy (XPS) analysis, and thermogravimetric analysis (TGA). Under partially-optimised conditions, >90 % recovery of Ru(III) from a 1 mM solution was achieved in ca. 8 h.

Remarkable adsorptive capacity and reusability performance of magnetic magnetite@silica@L-histidine nanocomposite towards gaseous benzene pollutant

Herein, magnetic magnetite@silica@L-histidine (Fe3O4@SiO2@L-Hist) core-shell nanoparticles (NPs) as novel adsorbents were first prepared via chemical co-precipitation and sol-gel technology for the adsorption of gaseous benzene pollutant. The Fe3O4, Fe3O4@SiO2 and Fe3O4@SiO2@L-Hist NPs were characterized using a combination of scanning electron microscopy (SEM), SEM - energy dispersive X-ray (SEM-EDX), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), vibrating sample magnetometry (VSM), Brunauer-Emmett-Teller analysis (BET), X-ray photoelectron spectroscopy (XPS) and thermal gravimetric analysis (TGA). The adsorption capacities of Fe3O4, Fe3O4@SiO2 and Fe3O4@SiO2@L-Hist NPs for benzene were found to be 188, 279 and 481 mg g-1, respectively, with Fe3O4@SiO2@L-Hist NPs demonstrating the highest capacity. Kinetic and isotherm studies indicated that the pseudo-2nd-order kinetic model and the Langmuir isotherm model provided the best fit to the experimental data, suggesting favorable physical adsorption. In addition, Fe3O4, Fe3O4@SiO2 and Fe3O4@SiO2@L-Hist NPs exhibited remarkable reusability, with reuse efficiencies of 85.67, 89.65 and 91.73%, respectively, after five recycle cycles, demonstrating their potential for practical benzene remediation applications. Overall, this study offers valuable insights into creating effective and sustainable adsorbents for eliminating volatile organic compounds (VOCs). This contributes to mitigating air pollution and safeguarding both human health and the environment.

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).

Stabilization of Arsenic and Heavy Metal Contaminated Soil Using Fishery By-Products and Evaluation of Heavy Metal Uptake in Crops

Objectives : Heavy metals eluted from mine waste pollute surrounding soil and water systems, which can spread to crops and have a harmful effect on the human body. The purpose of this study was to evaluate the feasibility of recycling discarded mussel shells(MS) and manila clam shells (MC) as stabilizers for the immobilization of arsenic(As) and heavy metals(Pb, Zn) in soil.Methods : MS and MC were processed with -#10 mesh natural material, -#20 mesh natural material, and -#10 mesh calcined material and treated at 0-10 wt%. After 1 week or 4 weeks of wet curing, it was eluted with 0.1 N HCl and the concentrations of As, Pb, and Zn in the soil were analyzed through inductively coupled plasma optical emission spectroscopy(ICP-OES) analysis. In addition, red lettuce was cultivated in the stabilized soil and the concentration of heavy metals that were transferred to crops was evaluated. The stabilization mechanism was investigated by scanning electron microscopy-energy dispersive X-ray spectroscopy(SEM-EDX) analysis.Results and Discussion : The stabilization efficiency for arsenic and heavy metals was in the order of natural -#10 mesh < natural -#20 mesh < calcined -#10 mesh. The calcined stabilizer showed a high stabilization efficiency of 98% at a 2 wt% treatment level. Pb was not detected in the red lettuce grown in the stabiliz ed soil, and the standard for leafy vegetables (Pb-0.3 mg/kg or less) was satisfied according to the Ministry of Food and Drug Safety. The SEM-EDX analysis revealed that As was stabilized through Ca-As precipitation and heavy metals(Pb, Zn) were stabilized through pozzolanic reactions.Conclusion : Stabilizers developed from MS and MC can be effectively applied to the stabilization of As and heavy metal-contaminated soil, and are expected to be used as economical and environmentally friendly stabilizers.

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.

Environmentally Benign Green Approach for the Aynthesis of IONPs Using <i>Vicia Faba</i> Fruit Extract and Their Antioxidant Activities

Iron oxide nanoparticles synthesized from plant materials have garnered considerable attention due to their environmentally friendly nature and wide-ranging applications in various fields. These NPs possess unique attributes, including biocompatibility, low toxicity, catalytic capabilities, and intricate reaction mechanisms, making them highly desirable for diverse biomedical uses. This study presents an innovative green synthesis approach for utilizing the fruit extract of Vicia faba (V. faba). The synthesized NPs underwent comprehensive characterization using advanced techniques such as Fourier-transform infrared spectroscopy (FTIR), UV-visible spectrophotometry, X-ray diffractometry (XRD), and Scanning Electron Microscope-Energy Dispersive X-ray (SEM-EDX). Notably, the V. faba fruit extract served as an effective reducing agent, facilitating the synthesis of Iron oxide nanoparticle (IONP) with well-defined structural and chemical properties. The size of Iron oxide nanoparticles falls between the range of 299.3-527.4 nm. Furthermore, the synthesized Iron oxide nanoparticles were evaluated for their antioxidant activity, revealing promising results against 2,2-diphenyl-1-picrylhydrazyl DPPH and 2,2’-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) ABTS radicals. These findings highlight the significance of V. faba fruit extract in producing IONPs endowed with valuable bioactive properties, offering considerable potential for applications in biomedicine and beyond.

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.

Comparative Analysis of Biochar Derived from Rice Straw and Soybean Straw

Aim: Recycling agricultural postharvest waste and re-introducing it again into farmland is one of the tangible ways to address zero waste dream, soil infertility and climate change. Pyrolysis of crop leftovers into biochar remains the most acceptable alternative for proper management of crop waste. The possibility of sustainable biochar production practices and multi-functionality features makes it promising to fufill an increasing demand for soil amendment, agricultural sustainability, environmental protection, cutting-edge materials and mitigation of climate change. Methodology: Same amount (14450 g) in feedstock of rice straw (RS) and soybean straw (SS) undergo slow pyrolysis separately to produce biochar. Physical (percentage yield, moisture, ash, volatile matter, bulk density, pH, electrical conductivity), chemical characterization (Microwave Plasma Atomic Emission Spectroscopy (MP-AES), Scanning Electron Microscope Energy Dispersive X-ray (SEM-EDX), Fourier Transformed Infrared (FTIR) and Thermogravimetric Analysis and Derivative Thermogravimetry (TGA and DTA)) and evaluation of bochar was determined. Results: Rice straw biochar (RSB) recorded a higher char yield of 42.1%. Both lignocellulosic biochars were black and porous with a higher silica (10.6%) content in RSB and higher carbon (82.2%) content in SSB as was revealed by SEM-EDX. Higher ash 27.1%, volatile matter (VM) 31.3% and moisture 29.4% content was seen in RSB compared to SSB because of feedstock composition. Rice straw biochar show higher peaks of macro and micro mineral elements K(14561.21mg/kg), Ca (2401.28 mg/kg), and Na(1735.27 mg/kg) than soybean straw biochar. FTIR was used to identify functional groups that might act as cation adsorbents. As the temperature increased, the TGA and DTG graphs showed mass loss and sample breakdown. Conclusion: Rice and soybean crop wastes were converted into biochar, a nutrient-rich material that maybe utilized to balance acidic soils promoting healthy plant growth and also protecting the environment.