Scanning Electron Microscopy-energy Dispersive Spectroscopy Research Articles

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.

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.

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 C=O double bond (carbonyl group) and carboxylic acid/ester bond (O−C=O) 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.

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.

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.

The effect of cobalt alloying on the phase transformation kinetics of Ni-Ti alloys

This study investigates the influence of cobalt (Co) alloying addition and heat treatment temperature on the phase transformation behaviour controlling the superelasticity and shape memory effect (SME) of Nickel-Titanium (Ni-Ti) alloys, commonly known as nitinol. The microstructural evolution upon heat treatment conducted at a temperature ranging from 440 to 560 °C was thoroughly analyzed via Differential Scanning Calorimetry (DSC), X-ray Diffraction (XRD), and Scanning Electron Microscopy/Energy Dispersive Spectroscopy (SEM/EDS). Increase in heat treatment temperatures from 470 °C up to 530 °C led to the dissolution of particles present in as-received (cold-worked) condition. It was determined that Co addition into the Ni-Ti alloy system resulted in a change in the nucleation and growth kinetics of Ti-rich precipitates, leading to the formation of larger and fewer particles during processing. Both binary and ternary alloys showed a decrease in austenite finish temperature (Af) with increasing heat treatment temperatures, however, the rate of decrease was found to be higher for Co containing ternary alloys. This is linked with faster structural relaxation when Co is present and evidenced by lattice size variation during heat treatment. It is highlighted that heat treatment methodology needs to be tailored to the specific alloy composition for controlling superelasticity and SME via alloy design.

Investigation on utilization and microstructure of fine iron tailing slag in road subbase construction

The iron tailing slag is solid waste produced during the iron ore refining process and is considered a potential hydraulic material that can be used in road construction. This study focused on fine iron tailing from a location in Hebei, China, to prepare road subbase specimen with a high proportion of fine iron tailing. The research investigated the effects of raw material ratios and additives on the 7-day unconfined compressive strength and elastic modulus of the specimens, as well as their mechanisms of action. A series of single-factor experiments were conducted using a controlled variable approach, including the mass ratio of slag to fly ash (SFR), cement content, and calcium oxide content. It was found that under the conditions of an SFR of 6:1, a calcium oxide content of 4 %, a cement content of 5 %, and a water-resistant base stabilizer additive of 0.02 %, the eco-friendly road subbase specimen achieved a 7-day unconfined compressive strength of 1.97 MPa and an elastic modulus of 286 MPa, demonstrating good mechanical properties. Additionally, a linear relationship was observed between the cement content and the 7-day unconfined compressive strength of the specimen: Rc = 0.253w + 0.793. Using characterization techniques such as X-ray Fluorescence Spectroscopy (XRF), X-Ray diffraction (XRD), Scanning Electron Microscope & Energy Dispersive Spectroscopy (SEM-EDS), and Fourier Transform Infrared Spectroscopy (FTIR), a dense structure was observed in the slag-based road subbase specimen, composed of needle-rod hydrated calcium silicate (C-S-H) gel, hydrated calcium aluminate (C-A-H), hydrated calcium silicoaluminate (C-A-S-H), flake-like hydrated magnesium silicate (M-S-H) gel, and a system containing a large amount of Forsterite. Finally, the study examined the impact mechanisms of five additives—Na2CO3, Na2O·2SiO2, triethanolamine (C6H15NO3), CaSO4, and a water-resistant base stabilizer—on the compressive strength and elastic modulus of the slag road base specimen. It was concluded that the water-resistant base stabilizer significantly improved strength and reduced water absorption. The road subbase specimen can be used by simply mixing at room temperature and pressure, offering broad prospects for industrial application. This technology provides a paradigm for the comprehensive utilization of fine iron tailing and the preparation of new road subbase materials.

Effective photocatalytic degradation of sulfamethoxazole using PAN/SrTiO3 nanofibers

Freshwater scarcity driven by pollution and climate change necessitates the development of effective water purification methods. There is an urgent need for innovative solutions that can efficiently remove contaminants from water sources. A effective material for the photocatalytic degradation of organic sulfonamide antibiotics from water was developed in this study. A composite of electrospun strontium titanate (SrTiO3) and carbon fibers polyacrylonitrile/strontium titanate (PAN/SrTiO3) was employed for the photocatalytic degradation of sulfamethoxazole (SMX). Scanning Electron Microscopy/Energy Dispersive Spectroscopy (SEM-EDS), Transmission electron microscopy (TEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) were used to characterise the composite. The fibers had a thickness of ~250 nm and uniformly dispersed PAN and SrTiO3 particles. A PAN/SrTiO3 composite with a 1:1 mass ratio (20 mg) demonstrated excellent performance, achieving over 90 % degradation at pH 7 and a contaminant concentration of 5 mg/L under ultraviolet (UV) light irradiation during 60 min. The composite was tested for the photodegradation of the major organic pollutant (SMX) in distilled and river water. In river water, the degradation efficiency exceeded 80 % at pH 7 because of the formation of secondary radicals involved in antibiotic degradation. SMX degradation was described using a pseudo-first order kinetic equation using the Langmuir-Hinshelwood model. These results underscore the novelty and significance of the PAN/SrTiO3 composite and demonstrate its high efficiency and potential for large-scale water purification applications.

Synergistic Antifungal Activity of Green Synthesized Zinc Oxide Nanoparticles and Fungicide Against Rhizoctonia solani Causing Rice Sheath Blight Disease.

The biosynthesis of metal oxide nanoparticles using leaf extract of medicinal plants is a promising substitute for the traditional chemical method. This work aimed to synthesize zinc oxide nanoparticles using a green approach from local "Dholkolmi" (Ipomoea carnea) leaf extract which is a medicinal plant growing outside the roads of different regions of Bangladesh. The biosynthesized zinc oxide nanoparticles (ZnONPs) were characterized using ultraviolet-visible spectroscopy, Fourier transform infrared spectroscopy, X-ray diffraction, particle size analyzer, zeta-potential, scanning electron microscopy-energy dispersive spectroscopy, field emission scanning electron microscopy, and transmission electron microscopy. The results of UV-visible spectrophotometers observed an absorption peak at 373 nm wavelength, which confirmed the synthesis of ZnONPs in the solution. ZnONP sizes determined by XRD, DLS, and TEM are approximately ~37 nm, 105.61 nm, and 19.66 nm, respectively. ZnONPs were present because of the strong oxygen and zinc signals in the EDX profile. Additionally, this research assessed the antifungal activity of the biosynthesized ZnONPs and as well as folicur-incorporated ZnONPs against Rhizoctonia solani by the poison bait technique. According to the result of this study, ZnONPs synthesized from Ipomoea carnea leaf extract showed no promising result against Rhizoctonia solani mycelial growth reduction. But folicur-incorporated ZnONPs revealed a significant finding with a maximum 100% inhibition of mycelial growth at 1:1 and 3:1 ratio of ZnONPs with folicur fungicide under in vitro conditions. In the net house experiment, folicur-incorporated ZnONPs at a 1:1 ratio of ZnONPs with folicur showed considerable disease inhibition (26.96% RLH) as compared to disease control (52.83% RLH). In the case of rainfed transplanted Aus (March-June), the highest percentage of RLH was recorded in disease control (64.61%), and the lowest RLH was found in folicur (24.79%) followed by a 1:1 ratio of ZnONPs with folicur (32.10%) in field condition. On the other hand, the highest percentage of RLH was recorded in disease control (65.31%) and the lowest RLH was found in folicur (18.14%) followed by a 1:1 ratio of ZnONPs with folicur (21.39%) in rainfed transplanted Aman (July-November) season. The findings of the in vitro and in vivo studies provided evidence that ZnONPs and folicur had a strong synergistic antifungal impact and may be employed as a possible rice sheath blight disease management agent.

Fabrication of Al-Ti intermetallic alloy via aluminothermic reduction process from TiO2 in molten salts

ABSTRACT A novel method based on the aluminothermic reduction of TiO2 in Na3AlF6-AlF3-CaF2 molten salts has been proposed to prepare Al-Ti intermetallic alloys in this research. The Al-Ti intermetallic alloy was obtained by reducing dissolved TiO2 in electrolyte molten salt using liquid Al as a reductant at the stirring rate of 200 r/min for 5 min under 960°C, and it was mainly enriched in the Al matrix which was dispersed in molten salts. The lower alloy layers in the melt pool were characterised by X-ray diffraction (XRD), scanning electron microscopy, energy dispersive spectroscopy (SEM-EDS), and X-ray photoelectron spectroscopy (XPS), taking advantage of the specific gravity difference between the molten salt and the alloy. The TiAl3 was the major intermetallic alloys phase formed between Al and Ti according to XRD results. The Al2O3 by-product in the reduction process of TiO2 was dissolved in electrolyte molten salt.

Construction biotechnology: improving mortar properties through calcium carbonate precipitation using a novel strain of the bacterium Neisseria perflava

In construction technology, there are significant efforts to reduce environmental emissions, particularly NH3 and other pollutants. This study marks the first application of CaCO3 biomineralization biotechnology in microbially induced calcium carbonate precipitation (MICCP) to enhance mortar properties using the non-pathogenic Neisseria perflava strain SKC/VA-3, which employs carbonic anhydrase mechanisms. The results demonstrated that N. perflava could significantly improve the physical and mechanical characteristics of mortar. Incorporating N. perflava and calcium lactate pentahydrate resulted in a 20% increase in compressive strength and a 14% rise in indirect tensile strength of the mortar. Examination through scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM–EDS) revealed calcite formation within the microstructure of the bio-mortar. Additionally, self-healing assessments indicated that calcite precipitation, driven by bacterial metabolism, also occurred on the cracked surfaces of the bacterial mortar, suggesting potential for reduced maintenance and increased material longevity. This study provides the first report on the use of N. perflava for bio-mortar enhancement and represents a novel biotechnological approach to improving the properties of mortar and other cementitious materials. The utilization of N. perflava in bio-mortar represents a groundbreaking biotechnological advance, potentially enhancing mortar and other cement-based materials. This development contributes to sustainable, durable, and environmentally friendly construction technologies.