Resonance Band Research Articles

Plant-assisted green preparation of silver nanoparticles using leaf extract of Dalbergia sissoo and their antioxidant, antibacterial and catalytic applications.

Plant-mediated preparation of silver nanoparticles (AgNPs) is thought to be a more economical and environmentally benign process in comparison to physical and chemical synthesis methods. In the present study, the aqueous leaf extract of Dalbergia sissoo was prepared and utilized to reduce silver ion (Ag+) during the green synthesis of silver nanoparticles (DL-AgNPs). The formation of DL-AgNPs was verified using UV-Vis spectra, exhibiting the surface plasmon resonance (SPR) band at around 450nm. FT-IR analysis revealed the kinds of phytochemicals that serve as reducing and capping agents while DL-AgNPs are being synthesized. Analysis of scanning electron microscope (SEM) and high-resolution transmission electron microscopy (HR-TEM) images verified the development of spherical and oval-shaped DL-AgNPs, with sizes ranging from 10 to 25nm. The stability and particle size distribution of synthesized DL-AgNPs were ensured by zeta potential and DLS (dynamic light scattering) investigations. Additionally, X-ray diffraction (XRD) analysis confirmed the crystalline nature of DL-AgNPs. In antioxidant experiments, DL-AgNPs demonstrated significant scavenging capacities of DPPH and ABTS radicals with EC50 values of 51.32 and 33.32μg/mL, respectively. The antibacterial activity of DL-AgNPs was shown to be significant against harmful bacteria, with a maximum zone of inhibition (21.5 ± 0.86mm) against Staphylococcus aureus. Furthermore, DL-AgNPs exhibited effective catalytic activity to degrade environment-polluting dyes (methylene blue, methyl orange, and Congo red) and toxic chemicals (p-nitrophenol). The results of all these studies suggested that DL-AgNPs made from the leaf extract of Dalbergia sissoo have merit for application in the environmental and biomedical fields.

Insights on the effect of process conditions on the optical properties of silver ion exchanged soda-lime silicate glass

The effects of ion exchange time and temperature on the optical properties and plasmonic response of silver ion exchanged soda-lime silicate glass were investigated using scanning electron microscopy (SEM) in energy dispersive spectrometry (EDS) configuration, m-lines spectroscopy, photoluminescence (PL) spectroscopy, and UV–visible absorption spectroscopy. SEM analyses in EDS mode provided profiles of silver oxide molar concentration. These profiles were directly correlated to the silver diffusion coefficient using an adjustment procedure. The effective indices of ion exchanged glasses measured by the standard prism coupling technique (m-lines) allowed access to refractive index distributions in ion exchange regions. These ion-exchanged glasses underwent evaluation to determine their potential suitability for use in multimode planar systems. The PL results acquired after ion exchange demonstrated that the creation of Ag0 atoms from Ag+ ions was responsible for the decline and quenching of PL intensity at ion exchange times and temperatures increase. Silver nanoparticles were generated in the samples subjected to ion exchange at 480 °C without the need for post-exchange treatments. The emergence of the surface plasmon resonance band around 427 nm in the optical absorption spectra confirmed the formation of Ag nanoparticles in annealed glasses. Estimates of the UV–visible absorption spectra indicated an average size of silver nanoparticles ranging from 1.8 to 2.4 nm.

Ag nanocubes-decorated ammonium hydroxide-treated carbon nitride to improve photocatalytic H2O2 production and fuel cell performance

A novel photocatalyst is designed by surface modification and cocatalyst loading of graphitic carbon nitride (g-C3N4) with ammonium hydroxide and silver nanocubes (AgNCs), respectively. The synergistic effect of the modification in the intralayer of g-C3N4 and surface plasmon resonance (SPR) bands of AgNCs significantly enhances the migration and separation efficiency of photo-induced charge carriers. A nickel mesh coated with photocatalyst and the carbon paper loaded with pristine g–C3N4–mixed iron phthalocyanine (FeIIPc) used as the photoanode and cathode, respectively, are constructed for the self-powered photoelectrochemical cell, which exhibits the maximum power density of 0.74 mW cm−2. The AHCN/AgNCs-based cell reveals approximately a 3.1-times enhancement in maximum power density compared with the pristine g–C3N4–based cell. In addition, the photocatalytically generated H2O2 (chemical energy) can be stored in water, and then used as fuel by the connection of two electrodes in the dark. After the fuel cell is operated for 12 h, the specific capacitance retention rate still maintains as high as 57.2 %, which is the greatest retention rate in comparison with the previously reported H2O2 fuel cell systems. Our work offers a feasible opinion on how to improve the visible light utilization of semiconductors by tuning the intralayer properties and loading plasmonic metal.

A compound reconfigurable electronically switched parasitic monopole antenna for sub 6 GHz wireless and vehicular applications

In this paper, a compound reconfigurable electronically switched parasitic monopole antenna is reported for sub-6 GHz (n77/n78 bands) wireless standards and vehicular communication. The antenna comprises a half-hexagonal-shaped radiating element and two inverted L-shaped parasitic stubs. These stubs are connected to two PIN diodes, allowing for control over frequency. An additional pair of PIN diodes incorporates analogous parasitic stubs into the ground plane to facilitate pattern tilting and polarization. By switching these PIN diodes across seven operating states (OS), the antenna structure could resonate in a single band, spanning 4.5–5.8 GHz (sub-6 GHz higher band), with an omnidirectional pattern specific to OS1. In OS2 and OS3, the antenna resonates in a single band within the range of 4.1–5.7 GHz, featuring beam tilting with linear polarization. In OS4 and OS5, the structure has two bands: one covers 3.3–4.2 GHz (5G-n77 band) with linear polarization, and the other covers 5.1–6.1 GHz (5G WLAN band) with right-hand circular polarization (RHCP) in OS5 and left-hand circular polarization (LHCP) in OS4 with an axial ratio bandwidth of 14.5 %, including pattern tilting within the range of ± 340. Finally, in the OS6 and OS7 structure introduce dual bands of 3.3–3.8 GHz (5G–n78 band) and 4.8–5.8 GHz (sub-6 GHz higher band). Both bands feature LHCP/RHCP with an axial ratio bandwidth of 8.57 % for the lower resonant band and 7.4 % for the higher resonant band. Additionally, it incorporates radiation pattern reconfiguration capabilities. The structure is printed on an FR-4 substrate and measures various associated parameters. The experimental results closely match the simulated results.

Development of PVA/sodium alginate incorporated with histidine capped silver nanoparticles for food packaging application

AbstractPackaging is a growing field of interest, and the use of nanotechnology is accelerating its expansion. The study reports the fabrication of poly(vinyl alcohol) (PVA) blended sodium alginate (SA) and incorporated with different ratios of histidine‐capped silver (H‐AgNPs) nanoparticle films. Fabrication of PVA/SA/H‐AgNPs films was confirmed with the surface plasmon resonance (SPR) band denoted AgNPs presence between 400 and 420 nm measured by UV–Vis absorption spectroscopy. The characteristics of the polymeric biocomposite films were significantly altered by different ratios of AgNPs. The interaction of PVA/SA and PVA/SA with AgNPs was analyzed by using FT‐IR analysis. The degree of crystallinity was increased upon increasing the concentration of H‐AgNPs as confirmed by XRD measurements. The homogeneity of dispersion and surface morphology of samples were studied by FESEM. The addition of H‐AgNPs in the polymeric film increased the surface roughness of the polymeric film confirmed by AFM analysis. The contact angle of the PVA/SA blend matrix was observed to be 46.97°, and with the incorporation of AgNPs ranging from 3%, 5%, and 7% to the blend matrix, the contact angle of the nanocomposite films in increasing hydrophobic order was 60.53°, 83.57°, and 96.20°, respectively. The incorporation of AgNPs also demonstrates that the PVA/SA blend matrix has desirable thermal stability. The improved qualities were due to H bonding between PVA, SA, and H‐AgNPs, in which molecules contact strongly with one another. Furthermore, the PVA/SA/H‐AgNPs showed significant antibacterial activity against both Gram‐positive (G+) strains (Staphylococcus aureus) and Gram‐negative (G−) strains (Escherichia coli) bacterial infections. The findings of this research indicate that the PVA/SA/H‐AgNPs fabricated composite films considerable for applications in food packaging.

Green synthesis of Abutilon indicum (L) derived iron oxide (FeO) nanoparticles with excellent biological, anticancer and photocatalytic activities

Cancer is one of the most common causes of death all over the world. Although there are many treatments available none of them are without side-effect and most of them are very expensive. Similarly, Inflammation is one of another common medical condition worldwide but most of the therapies available are not environment and pocket friendly. Thus, the aim of our study was to synthesize environmentally friendly, cost-effective FeO NPs with significant anticancer, anti-inflammatory, antibacterial properties. The green synthesis of Iron Oxide Nanoparticles (FeO NPs) using plant extract is one of the environmentally friendly, cost-effective, and a secure alternative to physical or chemical synthesis methods. In the present study we used Abutilon indicum leaf extract to synthesize the Ai-FeO NPs and performed various experiments to confirm the therapeutic potential of green synthesized Ai-FeO nanoparticles. In this method, an aqueous plant leaf extract (A. indicum: Ai) was used as a reducing and stabilizing agent for the synthesis of FeO nanoparticles. The synthesized Ai-FeO NPs were characterized by the ultraviolet–visible (UV–Vis) absorbance of the surface at a resonance band 415 nm. Fourier transform infrared (FTIR) spectroscopy study confirmed the inherent bioactive functional groups as capping and stabilizing agents for Ai-FeO NPs. The X-ray powder diffraction (XRD) spectra revealed crystalline nature of the NPs. Further, the synthesized NPs have been isolated in highly stable, crystalline nature with spherical shape having size 10–95 nm. In addition, the green synthesized Ai-FeO-NPs demonstrated dose-dependent antimicrobial, antioxidant, anti-inflammatory, and anticancer properties. The findings of this study suggested that A. indicum leaf extract mediated FeO nanoparticles could be potentially used as a therapeutic agent for many human diseases and breast cancer.

Antibacterial properties of synthesized Melaleuca cajuputi-leaf gold nanoparticles

Biosynthesized gold nanoparticles (AuNPs) were successfully synthesized by using Melaleuca cajuputi leaf extract, and their prospective antibacterial efficacy was assessed against Vibrio parahaemolyticus. TEM analysis revealed biosynthesized M. cajuputi gold nanoparticles (MC-AuNPs) were spherical in shape with a surface plasmon resonance (SPR) band observed at 535 nm and particle sizes ranging from 10–50 nm. The MC-AuNPs showed good antibacterial properties against V. parahaemolyticus with MIC and MBC values of 0.0075 g/mL.

Construction of AgI/PCN-224 Z-scheme heterojunction for efficient photocatalytic degradation of tetracycline hydrochloride: Pathways, mechanism and theoretical calculations

The construction of heterojunction structures is pivotal in enhancing carrier separation and photocatalytic activity. Hence, AgI/PCN-224 (APN-x composites) Z-scheme heterojunctions were successfully synthesised using an in-situ precipitation method. The direction of electron migration and the band structures of APN-x were comprehensively investigated using a combination of experimental approaches and density functional theory (DFT) calculations. Owing to the extensive visible-light absorption capabilities of PCN-224 and the high efficiency of photogenerated carrier separation in the Z-scheme heterojunction, the optimally developed APN-3 photocatalyst demonstrated exceptional photodegradation efficiency for tetracycline hydrochloride (TCH). The removal rate of TCH by APN-3 within 120 min reached 91.56%, approximately 4.64 times higher than that achieved by pure AgI. The photocatalytic degradation mechanism was explored using free radical trapping experiments, electron spin resonance (ESR) technology and band structure analysis. Degradation pathways and intermediate products were investigated using liquid chromatography–tandem mass spectrometry (LC–MS).

Properties of spectral characteristics of quasi-stationary electron states in an open multi-cascade nanostructure

The exact expressions for scattering matrix and transmission coefficient in open multi-cascade nanostructure are obtained. The theory of spectral characteristics of electron quasi-stationary states is developed in two approaches. For the nanostructure with GaAs wells and AlGaAs barriers, it is established that resonance bands appear in the N-cascade structure. Each one is formed by the energies of N states. Only the scattering matrix allows to unambiguously determine the resonance energies and resonance widths of all electron states in the multi-cascade structure. The approach of transmission coefficient, due to the collapse of resonances, gives the incomplete information about the spectral characteristics.

Evaluation of PVC@Silver Nanocomposite as Sensor for Low Limit Detection of Cadmium Ion By Surface Plasmon Resonance Based Method

AbstractThis study explores the development of a PVC@Silver nanocomposite for enhanced detection of cadmium ions in water samples. Various characterization techniques confirmed the successful incorporation of silver nanoparticles into the polyvinyl chloride (PVC) matrix across different concentrations (1–4%). X-ray diffraction revealed the face-centered cubic crystalline structure of the silver nanoparticles, with the intensities of the (111), (200), (220), and (311) peaks increasing with higher Ag concentrations. The average crystallite sizes ranged from 26.1 nm (3% Ag) to 30.0 nm (2% Ag). Dynamic light scattering showed nanoparticle sizes of 24–43 nm, while zeta potential values of -24 to -40 mV indicated reasonable colloidal stability. Brunauer–Emmett–Teller (BET) surface area analysis demonstrated a decreasing surface area from 30.09 m2/g (1% Ag) to 25.27 m2/g (3% Ag), attributed to pore filling by silver nanostructures. Significantly, the PVC@Silver nanocomposite facilitated sensitive detection of Cd(II) ions using surface plasmon resonance (SPR), exhibiting an SPR angle shift of 26.30° with intensity values ranging from 10.80 (4% Ag) to 12.19 (3% Ag). UV–vis spectra revealed a prominent surface plasmon resonance band at 420–430 nm, indicating the presence of silver nanoparticles. The optical band gap varied from 4.51eV (1% Ag) to 4.12eV (4% Ag).

Weak plasmonic photocatalysis in unsupported colloidal gold nanorods

Metal-semiconductor plasmonic nanosystems have the ability to extract photocarriers generated on colloidal gold nanoparticles efficiently through the Schottky junction. This process leads to effective visible light photocatalysis. However, due to the short lifespan of plasmon carriers, plasmonic loss occurs before extraction by the semiconductor and transfer to the adsorbent. We aim to investigate the direct transfer of plasmonic energy to adsorbed organic pollutants in visible light photocatalysis using unsupported colloidal gold nanorods (Au NRs). Our decision to use gold nanorods is based on their exceptional ability to harness a greater amount of visible light through their longitudinal surface plasmon resonance (LSPR) at 765 nm and transverse surface plasmon resonance (TSPR) band at 521 nm. Additionally, we conducted experiments to evaluate the photocatalytic capabilities under specific wavelengths, such as blue (405 nm), green (532 nm), and red (660 nm) lasers, to gain a better understanding of the -d-sp interband transition and the role of surface plasmon in photocatalysis. Surprisingly, unsupported Au NRs showed only weak plasmonic photocatalysis under all these excitations. With the help of supporting characterization tools, we observed that without semiconductor support, the photoexcited carriers over Au nanorods are not well separated, resulting in reduced photocatalysis.

Phyto-mediated synthesis of Ag, ZnO, and Ag/ZnO nanoparticles from leave extract of Solanum macrocarpon: Evaluation of their antioxidant and anticancer activities

Silver, zinc oxide, and silver/zinc oxide nanocomposites were prepared from the facile green process using Solanum macrocarpon leave extract. Ag and ZnO nanoparticles (NPs) were composited with the aim of enhancing the synergy for improved antioxidant and anticancer activities. In the synthesis process, the formation of Ag NPs was initially observed by a colour change and was confirmed by the appearance of surface plasmon resonance (SPR) bands. Based on the crystallographic analysis of the diffraction patterns, the phyto-capped silver NPs possessed a crystalline character, featuring a lattice structure of face-centered cubic (FCC) and an estimated crystallite size of around 7.2 nm. The formation of a hexagonal crystal structure of spherical morphology was confirmed for the ZnO, while the Ag/ZnO composite showed additional planes due to the silver nanoparticles in the cubic phase. The scavenging activities of 2,2-Diphenyl-1-picrylhydrazyl (DPPH) free radicals and their anticancer potency on normal HEK and cancerous HELA cells were examined in comparison to standard drugs. They demonstrated remarkable IC50 values that were better than the control drugs. This study provides helpful insight into the synergy between Ag and ZnO nanoparticles for the possible development of new anticancer and antioxidant agents.

Green synthesis of silver nanoparticles from Olea europaea L. extracted polysaccharides, characterization, and its assessment as an antimicrobial agent against multiple pathogenic microbes

Abstract Recent advances in nanoscience and nanotechnology have revolutionized the medical field, particularly in the treatment and prevention of disease. Silver nanoparticles (AgNPs) are considered one of the best supreme and most important nanomaterials with a variety of compulsive nanomaterial having diverse array of multifunctional bioapplications. The current study focuses on the green biosynthesis of AgNPs using polysaccharides extracted from Olea europaea leaves. The synthesized AgNPs were thoroughly analyzed and characterized using various spectroscopic and microscopic techniques including, UV-Vis spectroscopy, Fourier transform infrared spectroscopy (FTIR), X-ray diffraction, Energy dispersive X-ray (EDX), and Scanning electron microscopy (SEM). The absorption peak at 440 nm showed a high plasmon resonance band, confirming the formation of green AgNPs by the reduction of Ag+ ions to Ag0. FTIR analysis showed the appearance and extension of different functional groups. The results of EDX and SEM confirmed the synthesis of AgNPs with spherical shape, crystalline structure, and an average size of 64.42 nm. The biosynthesized AgNPs possessed improved antimicrobial activities, indicating the importance of biosynthesized NPs in the pharmaceutical industry. In addition, the biosynthesized AgNPs were biocompatible and exhibited anti-inflammatory activity (86.29%), almost similar to that of a standard drug (87.78%) at a concentration of 500 µL/mL. The polysaccharides obtained from O. europaea could be considered as effective reducing agent, leading to an environmentally friendly synthesis of stable and biologically important AgNPs with a wide range of applications.

Green synthesis of CdS/flaxseed mucilage nanocomposite films using gamma irradiation for packaging applications

Abstract The most common ways to produce nanoparticles are through chemical and physical processes, which can be expensive and environmentally hazardous. Using plant extracts (green synthesis) as reducing and capping agents is a simple, cost-effective, and environmentally friendly method of lowering the usage of dangerous chemicals in the synthesis of metal nanoparticles. This study covers the environmentally friendly synthesis of cadmium sulphide nanoparticles (CdS NPs) using a blend of flaxseed extracts (FM), polyvinyl alcohol (PVA), and chitosan (Cs). The composites are then exposed to gamma irradiation at doses of 20 kGy and 40 kGy. UV–VIS absorption spectroscopy, SEM, HRTEM, EDX, and FTIR were used to analyse the produced nanocomposite films. UV–Vis absorption spectra showed considerable surface Plasmon resonance (SPR) bands at 396–440 nm, indicating that CdS NPs had been successfully synthesized. A progressive red shift in wavelength was noted, along with the broadening of the absorption band as the irradiation dose increased. Transmission electron microscopy pictures revealed that the generated CdS nanostructures were dispersed as spherical nanoparticles with remarkable structural homogeneity. Tensile strength and elongation measurements of the films revealed that the inclusion of CdS NPs improved their mechanical properties. The addition of CdS NPs to the current blends limits biodegradation in soil. Thermal gravimetric analysis findings showed that CdS NPs included in FM/PVA films had improved thermal stability. The antimicrobial activities of the tested films were performed against Staphylococcus aureus, Escherichia coli, and Candida albicans. The results revealed that all of the films exhibited more antibacterial activity against S. aureus than the two others, with the highest activity observed in nanocomposites with a high concentration of CdS.

Plasmon-exciton interactions in ZnO/AuNPs heterostructure film for high photoconductivity

This study investigatesplasmon-exciton interactions within ZnO/AuNPs heterostructure films. Elemental, structural, and morphological analyses validate the successful formation of these films. The observed shift in the plasmonic resonance band and absorption edge otowards the red region the red region is attributed to strong surface plasmon damping influenced by exciton interactions within ZnO. Irradiation with blue light induces plasmonic electrons, generation in the ZnO/AuNPs film, enhancing electrical conductivity through interaction with ZnO excitonic states. UV light irradiating generates the electron-hole pair in the ZnO film and interacts with the free electrons in AuNPs. The ZnO/AuNPs heterostructure films hold promise for applications such as high-performance UV-photodetectors, photoactive layers in solar cells, light-emitting diodes, and energy storage devices.

Influence the diphenhydramine hydrochloride–sodium carboxymethyl cellulose complex for nanoaggregate formation

This study aimed to create nanoaggregates that improve the synergistic interaction between the opposing charges in drug-polyelectrolyte complexes. In this study, sodium carboxymethyl cellulose (NaCMC) polyelectrolytes and diphenhydramine hydrochloride (DPC) drug molecules were used to form the nanoaggregate. The aggregation behaviour of NaCMC-DPC complexes was determined by using conductivity methods. The critical micelle concentrations (CMC) of NaCMC were reduced from 0.737 to 0.337 g/l in the aqueous and 29.18 mg/l in the DPC. The modified Corrin and Harkins (CH) and Frahm's approaches evaluated the binding efficiency of the NaCMC-DPC interaction. NaCMC-DPC complexes were examined by transmission electron microscopy (TEM) and dynamic light scattering (DLS) techniques to conform to the formation of bilayer vesicles. Furthermore, we prepared the silver nanoparticles by using NaCMC-DPC complex mixtures. We demonstrated how NaCMC-DPC mixtures might influence the self-assembly of silver nanochain designs that differed from open "end-to-end" networks. The results indicated that the assembly of silver nanochains was regulated by a variation of electrostatic interactions inside the NaCMC-DPC components, which organized themselves around anisotropic nanochains surfaces. Among the optical properties altered by the linear assembly, the longitudinal surface plasmon resonance band at 624 nm has an enhanced redshift.

Robust dual-angle measurement in magnetization transfer spectroscopy by time-optimal control.

Magnetization transfer spectroscopy relies heavily on the robust determination of relaxation times of nuclei participating in metabolic exchange. Challenges arise due to the use of surface RF coils for transmission (high variation) and the broad resonance band of most X nuclei. These challenges are particularly pronounced when fast mapping methods, such as the dual-angle method, are employed. Consequently, in this work, we develop resonance offset and robust excitation RF pulses for 31P magnetization transfer spectroscopy at 7T through ensemble-based time-optimal control. In our approach, we introduce a cost functional for designing robust pulses, incorporating the full Bloch equations as constraints, which are solved using symmetric operator splitting techniques. The optimal control design of the RF pulses developed demonstrates improved accuracy, desired phase properties, and reduced RF power when applied to dual-angle mapping, thereby improving the precision of exchange-rate measurements, as demonstrated in a preclinical in vivo study quantifying brain creatine kinase activity.

Pharmacological Effect of In Vitro Antioxidant Property and Green Synthesis of Silver Nanoparticles (AgNPs) Utilizing Murraya koenigii Antibacterial Application

ABSTRACT Background: Nonessential heavy metals pose a significant threat to human health due to their toxicity. Mercury, in particular, is identified as a hazardous metal. The study aims to detect mercury using colorimetric analysis with Murraya koenigii, emphasizing the eco-friendliness of the method. Aims and Objectives: The primary objective is to detect mercury using a colorimetric analysis method employing Murraya koenigii. Additionally, the study aims to investigate the eco-friendliness of this detection method. Materials and Methods: Colorimetric analysis was conducted using Murraya koenigii to detect mercury. Ultraviolet-visible (UV-vis) spectroscopy was employed to detect the formation of silver nanoparticles (AgNPs), with a characteristic surface plasmon resonance (SPR) band observed. X-ray diffraction (XRD) data analysis was performed to determine the crystalline nature and size of AgNPs. Scanning electron microscopy (SEM) was utilized to visualize the morphology of AgNPs. Fourier transform infrared (FTIR) spectroscopy was employed to identify functional groups involved in reducing silver ions. Antibacterial properties of synthesized AgNPs were tested against various microorganisms, including Escherichia coli, Staphylococcus aureus, Streptococcus mutans, and Enterococcus faecalis. Results: Mercury was successfully detected using colorimetric analysis with Murraya koenigii. Formation of AgNPs was confirmed by UV-vis spectroscopy, with a characteristic SPR band at 418 nm. AgNPs were found to be crystalline with an average size of 5.20 nm, as determined by XRD analysis. SEM images revealed spherical and polycrystalline AgNPs. FTIR spectra indicated the involvement of the -OH group of compounds in the extract in reducing silver ions. Synthesized AgNPs exhibited antibacterial properties against various microorganisms. Conclusion: A sustainable and eco-friendly method for synthesizing AgNPs using Murraya koenigii extract was successfully developed. This method not only detected mercury but also demonstrated antibacterial properties against various microorganisms. The study underscores the health implications of nonessential heavy metals, emphasizing the importance of eco-friendly detection and mitigation methods.

Antibacterial and cytotoxicity activity of green synthesized silver nanoparticles using aqueous extract of naartjie (Citrus unshiu) fruit peels

The application of plant extracts in the green synthesis of silver nanoparticles (AgNPs) has attracted significant attention owing to their eco-friendliness and cost-effective features. However, nanoparticles synthesized from plant materials may also display unique physicochemical properties. This study described an improved synthesis process for silver nanoparticles (AgNPs) from the peel of the Citrus unshiu fruit, an agricultural waste product. In addition to evaluating the produced AgNPs' physico-chemical characteristics, the research also examines their antibacterial and cytotoxic/anticancer capabilities. The color change from yellow to dark brown was observed immediately when 20 ml of Citrus unshiu fruit peel extract was added to 0.5 g of silver nitrate. A surface plasmon resonance band at 424 nm revealed by ultra-violet spectroscopy was used as additional confirmation that AgNP had formed. The scanning electron microscope (SEM), and the transmission electron microscope (TEM), revealed spherical-shaped NPs with a mean size of 23 nm. Furthermore, X-ray diffraction (XRD) confirmed the high crystallinity of the obtained NPs while Fourier transform infrared spectroscopy (FTIR) confirmed the bioreducing capacity of the Citrus unshiu fruit peel extract. The minimum inhibitory concentration (MIC) (31.25 μg/mL) of AgNPs significantly revealed a strong dose-dependent antibacterial effect on Staphylococcus aureus and Bacillus cereus. In contrast, their impact on gram-negative bacteria, such as Escherichia coli and Salmonella typhimurium, displayed an MIC of 250 μg/mL. The assessment of cytotoxicity on human embryonic kidney cells (HEK293) and lung cancer cells (A549) through a 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide assay revealed no detectable cytotoxic effects. The IC50 values were determined as 37.73 ± 0.34 μg/mL for HEK293 and 56.37 ± 0.73 μg/mL for A549, indicating the absence of significant adverse impacts on these cell lines. The anticancer drug doxorubicin was used as a reference standard, and had an IC50 value of 1.22 ± 0.09 and 0.76 ± 0.12 μg/mL against HEK293 and A549 cells, respectively. The results show that AgNPs synthesized from Citrus unshiu fruit peel could serve as antibacterial agents that may in the future be optimized for us in for example nanofiltration systems.

Enhancing the Elastohydrodynamic Lubrication and Vibration Behavior of Rolling Bearings Using a Hybrid Bio-Grease Blended with Activated Carbon Nanoparticles

In recent years, bio-lubricants have received a growing interest for industrial applications. Still, a full-scale implementation in machinery lubrication requires a thorough evaluation of their performance through tribological and operational tests to stand upon their performance. Additionally, the promising outcomes achieved by nanoadditives in improving the performance of synthetic lubricants have prompted research efforts to identify suitable nanoadditives for bio-grease. This paper introduces a bio-grease from a hybrid vegetable oil and glycerol monostearate as a thickener for the lubrication of rolling bearings. Activated carbon nanoparticles (ACNPs) as nanoadditives were synthesized, characterized, and incorporated into the bio-grease at concentrations of 0.5, 1, and 2% by weight. Tribo-tests were conducted on these bio-grease blends, and running tests were carried out using 6006 ball bearings on a custom test rig. Throughout a 30-min test run under a radial load of 10% of the bearing’s dynamic load rating, mechanical vibrations and power consumption were measured and analyzed for each bearing. The bio-grease with ACNPs exhibited a substantial reduction in wear scar diameter (WSD) and coefficient of friction (COF), achieving improvements of up to 73.6 and 65%, respectively, in comparison to lithium grease. Furthermore, the load carrying capacity was enhanced by 200%. The study revealed a strong correlation between measured vibration amplitudes and the viscosity of the bio-grease. The absence of high frequency resonant bands in vibration spectra indicated that the test grease samples satisfied the conditions of elastohydrodynamic lubrication, and these findings were corroborated through calculations of the minimum oil film thickness.