Search Results (135)

The integration of nanoengineered materials into concrete systems has emerged as a promising strategy for enhancing structural performance and sustainability. This study presents a hybrid experimental-analytical investigation into the use of multilayer graphene as a smart admixture in high-performance concrete. The research combines mechanical testing, microstructural characterization, and a multi-objective optimization model to determine the optimal graphene dosage that maximizes strength gains while minimizing carbon emissions. Concrete specimens incorporating multilayer graphene (ranging from 0.01% to 0.10% by weight of cement) were tested over 7 to 90 days for compressive, tensile, and flexural strengths. Simultaneously, X-ray diffraction, scanning electron microscopy, and energy-dispersive X-ray analyses revealed crystallinity enhancement, pore densification, and favorable elemental redistribution due to graphene inclusion. A normalized composite objective function was formulated to balance three maximization targets—compressive, tensile, and flexural strength—and one minimization goal—carbon emission. The highest objective score (Z = 1.047) was achieved at 0.10% graphene dosage, indicating the optimal balance of strength performance and environmental efficiency. This dual-framework study not only confirms graphene’s reinforcing effects experimentally but also validates the 0.10% dosage through mathematical scoring. The outcomes position of multilayer graphene as a powerful additive for high-strength, low-carbon concrete, especially suited for infrastructure in hot and arid environments. The proposed optimization approach provides a scalable pathway for performance-based graphene dosing in future innovative concrete formulations. Full article

The citrate–nitrate method was employed to synthesize the magnesium chromite (MgCr₂O₄) spinel, followed by calcination at 700 °C for 3 h. The synthesized compound was analyzed using techniques including powder XRD, SEM-EDAX, FTIR, UV-DRS, and LCR Meter. The structural analysis was conducted using an X-ray diffractometer, which revealed the formation of the cubic crystal symmetry of the sample with the corresponding Fd-3 m space group. The average crystallite size of the sample was calculated around 15.38 nm. Using tetrahedral and octahedral positions, the lattice vibrations of the associated chemical bonds were identified using Fourier transform infrared (FTIR) spectroscopy. SEM (scanning electron microscopy) micrographs showed that the spherical nature of the particles and the constituent particles were between 10 and 40 nm in size. The optical bandgap value was evaluated using Tauc’s plot. Pellets of the powdered sample were prepared for determining the dielectric aspects, such as the dielectric constant (ε′) and tangent loss (tanδ), in the frequency range of 10 Hz–8 MHz at room temperature. The charge transport mechanism was explored from the complex impedance spectroscopy study. The obtained results indicate that magnesium chromite may be a potential candidate in the fabrication of sensors, micro-electronic devices, etc. Full article

In both fundamental and applied scientific exploration, nanostructured protective materials have garnered substantial interest owing to their multifaceted utilization in the fields of medicine, pharmaceuticals, and electronics, among others. This study investigated the evolution of cutting-edge materials for electromagnetic radiation attenuation, with a specific emphasis on the incorporation of superparamagnetic magnetite nanoparticles, Fe₃O₄, into composite systems. The nanoparticles were generated through chemical condensation, meticulously adjusting the proportions of iron salts, specifically FeSO₄·7H₂O and FeCl₃·6H₂O, in conjunction with a 25% aqueous solution of ammonia, NH₄OH·H₂O. This study examined the intricate details of the crystalline structure, the precise composition of phases, and the intricate physicochemical attributes of these synthesized Fe₃O₄ nanoparticles. The analysis was conducted employing a suite of advanced techniques, including scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and energy-dispersive analysis (EDAX). The key findings of this research suggest that the magnetic nanoparticles generated through chemical condensation have an average size between 10 and 11 nm. This size was determined using BET surface area measurements, which were precise to within 0.1 nm. Moreover, this study demonstrated that incorporating superparamagnetic nanoparticles into composite materials significantly reduces microwave radiation. In particular, an optimal concentration of 0.25% by weight leads to a maximum decrease of 21.7 dB in cement specimens measuring 10 mm in thickness. Moreover, a critical threshold concentration of 0.5 weight percent is established, beyond which the interactions of nanoparticles inhibit the process of remagnetization. These investigations demonstrate that it is feasible to pursue a route towards the development of highly effective electromagnetic shielding materials tailored to specific requirements for diverse applications. Full article

Background: The durability of computer-aided design/computer-aided manufacturing (CAD/CAM) resin nanoceramics in the oral environment is influenced by aging factors such as thermocycling and ultraviolet (UV) exposure. This study investigates the impact of these aging processes on surface characteristics and repair bond strength. Methods: CAD/CAM resin nanoceramic samples were divided into the following five groups: control (non-aged), 1-year and 5-year thermocycling, and 1-year and 5-year UV aging (n = 12). For the thermocycling procedure, the parameters employed were a temperature range of 5–55 °C with dwell times of 20 s per bath and 10,000 and 50,000 cycles; for the ultraviolet aging process, the parameters were established at a wavelength of 340 nm, an intensity of 0.55 W/m², and durations of 300 h and 1500 h. Surface roughness, microhardness, and repair bond strength were analyzed through profilometry, Vickers microhardness testing, and shear bond strength assessment, respectively. SEM, AFM, and XRD analyses were performed for structural evaluation. Results: Both thermocycling and UV aging significantly increased surface roughness (p < 0.001) while reducing microhardness and repair bond strength (p < 0.001). UV aging had a more pronounced effect, particularly after five years, leading to the highest surface roughness (Ra: 61.77 μm; Rz: 271.57 μm) and lowest microhardness properties (63.13). EDAX analysis indicated matrix degradation and an increase in inorganic filler exposure. Conclusions: Aging significantly affects the surface characteristics of CAD/CAM resin nanoceramics, with UV aging exhibiting the most detrimental impact. These findings highlight the necessity of considering long-term material stability in dentistry. Full article

Cobalt–chromium (CoCr) alloys are frequently used to produce customized dental applications such as crowns, bridges, or prostheses. These medical products have anatomical forms, and can be effectively manufactured using the laser-based powder bed fusion (PBF-LB/M) technique. A major disadvantage of this approach is the extended time required to refine the resultant surface. The purpose of this research is to reduce the surface roughness of PBF-LB/M/CoCr dental crowns by adopting drag finishing (DF) technology. To evaluate the impact of this automatic post-processing, surface roughness measurements and geometrical investigations were undertaken. The microstructure was characterized using scanning electron microscopy (SEM), and the chemical composition was verified by energy-dispersive X-ray spectroscopy (EDAX). On outside surfaces, the DF post-processing decreased the initial surface roughness by 70–90%. The dental crown’s surface roughness value after DF post-processing was comparable to that of the basic form (cylinder). The lowest roughness was obtained with DF3 post-processing (Ra~0.60 μm). The inner surfaces were limitedly finished. The 3D surface texture showed that the DF method reduced the height of peaks, uniformizing the surfaces. CMM work compared the deviations between the virtual model and the printed samples before and after DF post-processing. This analysis revealed that dimensional deviations were reduced on the outside crown walls, ranging from +0.01 to +0.05 mm. The laser parameters and the heat treatment applied increased the hardness of CoCr crowns to 520 HV, but the proper DF conditions identified reduced the surface roughness and improved the accuracy. Full article

Despite the widespread use of Mg and Al alloys among light metals in the automobile and aviation industries, they have low tensile and fatigue strength. Therefore, in the present work, AZ91 Mg and AA6063 Al alloys were coated with a multilayer transition metal nitride film (Cr/CrN/TiCrN/TiCrCN) to increase fatigue and tensile strength. Films with Cr/CrN/TiCrN/TiCrCN microstructure architecture were synthesized on the surfaces of AZ91 Mg and AA6063 Al alloys using the CFUBMS (closed-field unbalanced magnetron sputtering) system, one of the PVD (physical vapor deposition) techniques. Films’ structural properties were analyzed by XRD, SEM, and EDAX, whereas mechanical properties were investigated using tensile and rotary bending fatigue testing machines. According to the SEM examination, the Cr, CrN, TiCrN, and TiCrCN multilayer nitride films on the two alloys have a columnar and dense microstructure. The XRD analysis detected Cr (211), CrN (111) and (200), TiN (111), (200) and (222), and TiCN (200) and (311) diffraction peaks. The Cr/CrN/TiCrN/TiCrCN multilayer coating increased the fatigue limit value of AZ91 by 11.22% from 70.26 MPa to 78.15 MPa. The fatigue limit value of AA6063 decreased by 9.79% from 79.71 MPa to 71.9 MPa. After coating, the tensile strength value of AZ91 increased from 137.89 MPa to 139.65 MPa, while the tensile strength of AA6063 decreased from 129.35 MPa to 118.16 MPa. Full article

Chitosan-based biosorbents are particularly valuable in environmental applications, such as wastewater treatment for contaminant removal. However, several challenges remain in optimizing their production and performance related to improving adsorption efficiency, stability, scalability, cost, and sustainable sourcing for large-scale applications. The removal of Methylene Blue (MB) and Orange 16 (O16) from aqueous solutions was studied using a biosorbent derived from the waste biomass of the brewing industry, specifically Saccharomyces pastorianus immobilized into chitosan. The biosorbent (obtained by a straightforward entrapment technique) was characterized using Scanning Electron Microscopy (SEM) and Energy Dispersive X-ray Analysis (EDAX) to evaluate its structural properties. The biosorption behavior toward organic contaminants, specifically a cationic and an anionic dye, was investigated. Key operational factors that influenced the biosorbent’s efficiency were examined, including the initial dye concentration, dye type, pH of the aqueous solution, and the amount of biosorbent used. These factors were evaluated during the initial stage of the biosorption studies to assess their impact on the overall performance and effectiveness of the biosorbent in removing the dyes from aqueous solutions. Using this eco-friendly biosorbent, the biosorption capacities obtained using the Langmuir isotherm model were 212.77 mg/g in the case of MB dye and 285.71 mg/g in the case of O16 mg/g, and the results confirmed that the biosorption process is based on a physical mechanism as suggested by the energy values of the process, E, obtained using the DR model: the obtained values of 6.09 kJ/mol (MB dye) and 7.07 kJ/mol (O16 dye) suggest a process based on electrostatic interaction bonds. These results indicate that residual biomass of Saccharomyces pastorianus, as a byproduct of a biotechnological process, can be exploited as a biosorbent by immobilization in an organic matrix (chitosan) for the retention of polluting organic species from the aqueous environment present in aqueous solutions in moderate concentrations. Full article

In this study, ZnO nanoparticles (ZnO NPs) were synthesized using a green method employing fresh Citrus aurantium L. aqueous extract (CA) as a reducing agent. After preparation, the ZnO NPs were characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy-dispersive X-ray analysis (EDAX), X-ray diffraction (XRD), and infrared spectroscopy (IR). The products displayed irregular particle shapes on a nanoscale. The adsorption ability of ZnO NPs was tested with amaranth red dye, and the result showed that it had a satisfied capacity for amaranth red. The adsorption data followed the pseudo-second-order model and the Langmuir model, which indicated the adsorption process was controlled by a chemical adsorption process and occurred homogeneously on the surface of absorbents. In addition, the prepared ZnO NPs also exhibited antibacterial abilities against Staphylococcus aureus and Escherichia coli bacteria; antioxidant activities were observed in 2-2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2′-azino-di(3-ethylbenzthiazoline sulphonate) (ABTS) radicals scavenging assays and the ferric ion reducing antioxidant power (FRAP) assay, which were better than those of traditional ZnO NPs except in the FRAP assay. Based on these findings, the ZnO NPs fabricated with CA aqueous extract displayed promising abilities in the environmental remediation of dye wastewater. Full article

This research study investigated the production and properties of zinc oxide (ZnO) nanoparticles derived from corn husks and their priming effects on wheat plant proliferation and antioxidant mechanisms compared to the nutri-priming technique under regular irrigation and drought-stressed conditions. Transmission and scanning electron microscopy (TEM and SEM), energy-dispersive X-ray spectroscopy (EDAX), and X-ray diffraction confirmed the nanoparticles’ hexagonal morphology and typical dimensions of 51 nm. The size and stability of these nanoparticles were assessed through the size distribution and zeta potential analysis, indicating reasonable stability. Fourier-transform infrared spectroscopy (FTIR) detected the newly formed functional groups. This study emphasized the role of reactive oxygen species (ROS) and phenolic compounds in plant responses to nanoparticle treatment, particularly in detoxifying harmful radicals. The research also examined the activity of antioxidant enzymes, including peroxidase (POX), catalase (CAT), and glutathione reductase (GR), in alleviating stress caused by oxidation while subjected to various treatments, including micronutrient seed priming with DR GREEN fertilizer. Some biochemical compounds, such as total phenolics (TPCs), total flavonoids (TFCs), and total hydrolysable sugars, were estimated as well to show the effect of the different treatments on the wheat plants. The findings suggested that ZnO nanoparticles can enhance antioxidant enzyme activity under certain conditions while posing phytotoxic risks, underscoring the complexity of plant–nanoparticle interactions and the potential for improving crop resilience through targeted micronutrient applications. Full article

Biocides are often used in various industries and applications to control microbial growth and prevent the deterioration of materials, and they often have the ability to target a wide range of microorganisms rather than being specific to one type. They are designed to be highly effective at killing or inhibiting the growth of microorganisms and some biocides have residual activity, meaning they remain active for a period of time after application, providing longer-term protection. Biocides need to be compatible with the materials and surfaces they are applied to without causing damage or adverse effects, and they should remain stable under various environmental conditions, such as temperature and pH, to maintain their efficacy over time. In this study, microcapsules incorporating the biocide 4,5-dichloro-2-n-octyl-4-isotriazolin-3-one (DCOIT) were synthesized, and their effectiveness was evaluated. The investigation focused on several aspects, including colloidal chemical properties such as interfacial tension at pH values of 3, 7, and 9, as well as the size, ζ-potential, and morphology of the microcapsules. To validate the microcapsule production, elemental analysis was performed, and the effects on wettability and toxicological properties were assessed within the DCOIT + trimethoxysilyl propylmethacrylate/silicon dioxide nanoparticle system. Interfacial tension kinetics were measured using the PAT-1 tensiometer. The microcapsules exhibited an average diameter of 146 ± 1 nm following emulsification, with a ζ-potential of −50.2 ± 1 mV, as determined by the Malvern Zetasizer Nano Z. The morphology of the microcapsules was characterized using the SEM Controller 1550. Elemental composition was analyzed via energy-dispersive X-ray microanalysis (EDAX). The study concluded that the DCOIT biocide, when incorporated in the TPM/SiO₂ system, demonstrated non-toxic properties. Full article

Nanoparticles derived from biological sources are currently garnering significant interest due to their diverse range of potential applications. The purpose of the study was to synthesize Al-doped nanoparticles of zinc oxide (ZnO) from leaf extracts of Cucumis maderaspatanus and assess their antioxidant and antimicrobial activity using some bacterial and fungal strains. These nanoparticles were analyzed using X-ray diffraction (XRD), ultraviolet–visible (UV-vis) spectroscopy, Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) with energy dispersive X-ray analysis (EDAX), transmission electron microscopy (TEM), and thermogravimetric analysis/differential thermal analysis (TG-DTA). The average crystalline size was determined to be 25 nm, as evidenced by the XRD analysis. In the UV-vis spectrum, the absorption band was observed around 351 nm. It was discovered that the Al-ZnO nanoparticles had a bandgap of 3.25 eV using the Tauc relation. Furthermore, by FTIR measurement, the presence of the OH group, C=C bending of the alkene group, and C=O stretching was confirmed. The SEM analysis revealed that the nanoparticles were distributed uniformly throughout the sample. The EDAX spectrum clearly confirmed the presence of Zn, Al, and O elements in the Al-ZnO nanoparticles. The TEM results also indicated that the green synthesized Al-ZnO nanoparticles displayed hexagonal shapes with an average size of 25 nm. The doping of aluminum may enhance the thermal stability of the ZnO by altering the crystal structure or phase composition. The observed changes in TG, DTA, and DTG curves reflect the impact of aluminum doping on the structural and thermal properties of ZnO nanoparticles. The antibacterial activity of the Al-ZnO nanoparticles using the agar diffusion method showed that the maximum zone of inhibition has been noticed against organisms of Gram-positive S. aureus compared with Gram-negative E. coli. Moreover, antifungal activity using the agar cup method showed that the maximum zone of inhibition was observed on Aspergilus flavus, followed by Candida albicans. Al-doping nanoparticles increases the number of charge carriers, which can enhance the generation of reactive oxygen species (ROS) under UV light exposure. These ROS are known to possess strong antimicrobial properties. Al-doping can improve the crystallinity of ZnO, resulting in a larger surface area that facilitates more interaction with microbial cells. The structural and biological characteristics of Al-ZnO nanoparticles might be responsible for the enhanced antibacterial activity exhibited in the antibacterial studies. Al-ZnO nanoparticles with Cucumis maderaspatanus leaf extract produced via the green synthesis methods have remarkable antioxidant activity by scavenging free radicals against DPPH radicals, according to these results. Full article

Community drinking water sources are increasingly contaminated by various point and non-point sources, with emerging organic contaminants and microbial strains posing health risks and disrupting ecosystems. This study explores the use of zinc oxide nanoparticles (ZnO-NPs) as a non-specific agent to address groundwater contamination and combat microbial resistance effectively. The ZnO-NPs were synthesized via a green chemistry approach, employing a sol-gel method with lemon peel aqueous extract. The catalyst was characterized using techniques including XRD, ATR-FTIR, SEM-EDAX, UV-DRS, BET, and Raman spectroscopy. ZnO-NPs were then tested for photodegradation of quinoline yellow dye (QY) under sunlight irradiation, as well as for their antibacterial and antioxidant properties. The ZnO-NP photocatalyst showed significant photoactivity, attributed to effective separation of photogenerated charge carriers. The efficiency of sunlight dye photodegradation was influenced by catalyst dosage (0.1–0.6 mg L⁻¹), pH (3–11), and initial QY concentration (10–50 mg L⁻¹). The study developed a first-order kinetic model for ZnO-NPs using the Langmuir–Hinshelwood equation, yielding kinetic constants of equilibrium adsorption and photodegradation of Kc = 6.632 × 10⁻² L mg⁻¹ and kH = 7.104 × 10⁻² mg L⁻¹ min⁻¹, respectively. The results showed that ZnO-NPs were effective against Gram-positive bacterial strains and showed moderate antioxidant activity, suggesting their potential in wastewater disinfection to achieve sustainable development goals. A potential antibacterial mechanism of ZnO-NPs involving interactions with microbial cells is proposed. Additionally, Gaussian Process Regression (GPR) combined with an improved Lévy flight distribution (FDB-LFD) algorithm was used to model QY photodegradation by ZnO-NPs. The ARD-Exponential kernel function provided high accuracy, validated through residue analysis. Finally, an innovative MATLAB-based application was developed to integrate the GPR_FDB-LFD model and FDB-LFD algorithm, streamlining optimization for precise photodegradation rate predictions. The results obtained in this study show that the GPR and FDB-LFD approaches offer efficient and cost-effective methods for predicting dye photodegradation, saving both time and resources. Full article

Thorium is a weak radioactive element, but the control of its concentration in natural aqueous systems is of great interest for health, because it is a toxic heavy metal. The present paper presents the recovery of thorium from diluted synthetic aqueous systems by nanofiltration. The membranes used for the nanofiltration of systems containing thorium species are composites containing 4′-Aminobenzo-15-crown-5 ether (ABCE) and sulfonated poly–etherether–ketone (sPEEK). The composite membranes (ABCE–sPEEK) were characterized by scanning electron microscopy (SEM), energy-dispersive X–Ray spectroscopy (EDAX), thermal analysis (TG and DSC), and from the perspective of thorium removal performance. To determine the process performance, the variables were the following: the nature of the composite membrane, the concentration of thorium in the aqueous systems, the rotation speed of the stirrer, and the pressure and the pH of the thorium aqueous system. When using pure water, a permeate flux value of 12 L·m⁻² h⁻¹ was obtained for the sPEEK membrane, and a permeate flux value of up to 15 L·m⁻² h⁻¹ was obtained for the ABCE–sPEEK composite membrane. The use of mechanical stirring, with a propeller stirrer, lead to an increase in the permeate flux value of pure water by about 20% for each of the studied membranes. Depending on the concentration of thorium and the pH of the feed solution, retentions between 84.9% and 98.4% were obtained. An important observation was the retention jump at pH 2 for the ABCE–sPEEK composite membrane. In the paper, a thorium ion retention mechanism is proposed for the sPEEK membrane and the ABCE–sPEEK composite membrane. Full article

The durability of geopolymer concrete containing Ground Granulated Blast Furnace Slag (GGBS) and Rice Husk Ash (RHA), along with Lightweight Expanded Clay Aggregate (LECA), was investigated. Six different LWGPC mixtures were made with NaOH molarities of 8, 10, and 12M. For each molarity, two combinations of source materials were selected: 100% GGBS (G) and 80% GGBS with 20% RHA (RG). In all the mixtures, coarse aggregate was substituted with 35% LECA. LWGPC mixtures were exposed to 3% HCl, 5% MgSO₄, and 3.5% NaCl for studying the durability properties. The test results demonstrate that 100% GGBS with 12M NaOH (12G) outperformed all other mixtures. The residual compressive strength of 12G mix LWGPC specimens after six months of exposure was found to be 86.4% in an acid environment, 90.6% in a sulfate environment, and 91.4% in a salt environment. The elemental composition analyzed using EDAX reveals that silica, alumina, calcium, and sodium are the predominant elements that form a dense microstructure with N-A-S-H, C-A-S-H, and C-S-H. Further, the inner properties of the specimens exposed to chemicals were examined using MATLAB R2023b and ImageJ 1.54f based on SEM images. The SEM image showed that the porosity of LWGPC specimens ranged from 0.5194 to 0.6748 µm, signifying an enhanced durability performance. The experimental results and microstructural analysis show that the LWGPC incorporating RHA and GGBS with LECA offers a superior performance, making it a promising solution for sustainable and durable construction. Full article

Background/Objectives: Phloroglucinol (PHL), a phenolic compound extracted from the brown alga Rosenvingea intricata, exhibits potent antioxidant and anticancer properties. This study aims to extract, purify, and characterize PHL, and further develop functionalized zinc oxide nanoparticles (ZnO NPs) loaded with PHL to enhance its therapeutic potential. Methods: PHL was extracted using acetone and purified through Sephadex LH-20 column chromatography, yielding a highly enriched fraction (F-3). The purified compound was characterized by FTIR, HPLC, NMR, and LC-MS. ZnO NPs were synthesized, PEGylated, and conjugated with PHL, forming ZnO-PEG-PHL NPs. Their characterization included DLS, zeta potential, XRD, SEM-EDAX, and encapsulation efficiency studies. Antioxidant assays (DPPH, FRAP, ABTS, RPA) were performed and in vitro cytotoxicity on A549 lung cancer cells were determined to evaluate the therapeutic efficacy of PHL. Results: The purified PHL fraction showed a high phenolic content (45.65 PHL mg/g), which was was confirmed by spectral analysis. The ZnO-PEG-PHL NPs increased in size from 32.36 nm to 46.68 nm, with their zeta potential shifting from −37.87 mV to −26.82 mV. The antioxidant activity was superior for the ZnO-PEG-PHL NPs in all assays, while the in vitro cytotoxicity tests showed an IC₅₀ of 40 µg/mL compared to 60 µg/mL for the ZnO NPs and 70 µg/mL for PHL. Apoptotic studies revealed significant cell cycle arrest and apoptosis induction. Conclusions: The synthesized ZnO-PEG-PHL NPs demonstrated enhanced antioxidant and anticancer properties, making them promising candidates for cancer therapy and antioxidant applications. Full article