Ultraviolet-visible Spectrophotometer Research Articles

An evaluation of antimicrobial potency of silver nanoparticles synthesised from Fusarium sp.

Biological synthesis of metal nanoparticles has caught the interest of scientists due to the environment friendly synthesis approach which yields metallic nanoparticles with antimicrobial potency. In the present study silver nanoparticles were produced using a green method with the assistance of Fusarium sp. fungal cell filtrate and their antimicrobial potency was explored. The silver nanoparticles depicted a surface plasma resonance of 434 nm when run in the Ultra Violet–Visible Spectrophotometer. The functional group present in the nanoparticles were investigated using an Attenuated Total Reflectance-Fourier Transform Infrared where –OH, C–H, amide I and amide II functional groups were notable. The morphology and crystallinity of the produced silver nanoparticles was investigated with the help of a Scanning Electron Microscope and X-ray Diffraction. The X-ray diffraction results revealed that the nanoparticles were crystalline in nature with a face centred cubic structure and a crystallite size of 38.5 nm. The Scanning Electron Microscope revealed that the nanoparticles were spherical with sizes ranging between 3 to 43 nm. Antimicrobial studies of the synthesised silver nanoparticles were conducted at different concentrations (1 mM, 10 mM, 20 mM and 100 mM) against disease causing microorganisms Bacillus subtilis, Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa, the results showed that at a concentration of 1 mM there was no inhibition but as the concentration was increased to 20 mM and 100 mM, there was a notable inhibition with the maximum inhibition zone being 17 ± 0.6 mm.

Antibacterial Effect of Nanoparticles Synthesized from Ficus exaseprata (Sandpaper Leaves)

The eco-friendly, cost effectiveness, and the less toxic nature of synthesized green nanoparticles to the environment have become a global attraction to many studies. The study aim to synthesize Silver (Ag) nanoparticles from Ficus exasperata (Sandpaper leave) leaves and to determine its antimicrobial effect on bacteria isolates. Silver (Ag) nanoparticles were synthesized from the plant extracts using standard extracting techniques and their presence was verified and confirmed using an ultraviolet-visible (UV-Vis) Spectrophotometer. A prepared series of silver nitrate (AgNO3) solutions were mixed with the plant extracts at a ratio of 1:1 (v/v) to a total volume of 20ml in a text-tube. The test tubes were rapped with aluminum foil and heated in a water bath at 60OC for 3 hours and allowed to cool and analyzed using UV-Vis Spectrophotometer. The UV-Vis spectra confirmed the different concentrations of silver nitrate (AgNO3) that produced Ag nanoparticles and their average size was more than 50nm and less than 100nm. The mixture of the leave extract was tested for its antimicrobial activity against gram-positive and gram-negative organisms such as Staphylococcus aureus Bacillus cereus and Escherichia coli respectively. The results showed that the growth of the different bacteria was inhibited by the extracts containing silver nitrate on Staphylococcus aureus and Escherichia coli and not on Bacillus cereus using Ficus exaseprata nanoparticles. Statistical evaluation showed that zones of inhibition on the three bacteria produced by the aqueous leave extracts containing different concentration of silver nitrate (AgNO3¬¬) precursor was significantly different from the silver nitrate (AgNO3) precursor. It were observed that the higher the concentration of the silver nitrate (AgNO3) the greater the zone of inhibition. It can be concluded that Ficus exaseprata leave extracts dope with silver nanoparticles, can produce antimicrobial effects on some microorganisms.

Contribution of extractives to the bark color of Caesalpinia sappan

The purpose of this study was to investigate the contribution of Caesalpinia sappan (sappan wood) bark extractives by analyzing color change of the bark after extraction and the color of the extracts with several color measurement methods. Successive extraction was performed with n-hexane, ethyl acetate, methanol, and hot water. Color change of the bark was measured using CIELab color system and the extracts were analyzed with Ultraviolet-Visible Spectrophotometer, total phenolic content (TPC), and Gas Chromatography Mass Spectrometry (GC-MS). The results showed that the highest change on the bark color after methanol extraction with the Δa* and Δb* values of -2,53 ± 0,60 and -3,64 ± 1,20 respectively. Also, methanol extract showed the highest total phenolic content (860,24 ± 30,19 mg GAE/g). In addition, the Ultraviolet-Visible is analysis showed a peak at 478 nm in the hot-water soluble extract and two peaks in the methanol soluble extract at 396 nm and 478 nm. Hydroquinone was detected as one of the major compounds by Gas Chromatography Mass Spectrometry in the methanol soluble extract. It was suggested that the color of Caesalpinia sappan (sappan wood) bark as well as the deep red coloration of its extract might be contributed by multiple phenolic compounds contained in the methanol extract with hydroquinone as its precursor. Therefore, it is also a potential source for coloring matter.

Photocatalytic Degradation of Methylene Blue Dye by Using Different Nanoparticles

Zinc sulfide nanoparticles (NPs) were produced through a straightforward and cost-efficient chemical co-precipitation technique, intended for use in the photocatalytic decomposition of methylene blue (MB) dye, both under ultraviolet and visible light exposure. To evaluate the synthesized nanoparticles, various analytical tools including ultraviolet-visible (UV-Vis) spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray diffractometry (XRD) were employed. The XRD analysis confirmed the cubic symmetry of the synthesized NPs. SEM analysis revealed that the nanoparticles tend to aggregate, forming clusters of nanoparticles. TEM analysis illustrated that the ZnS nanoparticles exhibit a spherical morphology with uniform size distribution. Additionally, Fourier-transform infrared (FTIR) analysis exhibited a vibrational peak at 616 cm-1. The degradation of methyl blue was investigated using a UV-Vis spectrophotometer as part of the study.

An evaluation of the pharmacological responses of metal nanoparticles derived from aqueous extract of Caralluma adscendens R. Brown var. Bicolor

Nanomaterials employed in nanomedicine have the potential to function as both diagnostic and therapeutic tools for individuals. Over the past few decades, significant efforts have been made to synthesize a range of metal nanoparticles through the utilization of different plant extracts. Caralluma adscendens R. Brown var. bicolor leaves (CABL) extract was employed in this study as a reducing/capping agent for the synthesis of gold/silver nanoparticles (CABL@AgNPs/CABL@AuNPs) and explore their pharmacological properties. The successful synthesis of CABL@AgNPs and CABL@AuNPs was confirmed through the observation of surface plasmon resonance (SPR) at 439 and 522 nm using ultraviolet–visible spectrophotometer (UV–Vis). High resolution-transmission electron microscopy (HR-TEM) and energy dispersive X-ray (EDX) techniques were employed to evaluate the shape, size, and chemical composition of the as-synthesized CABL@AgNPs and CABL@AuNPs. Fourier-transform infrared spectroscopy (FTIR) was used to determine the biomolecules responsible for the reduction of metal ions and the stability of metal nanoparticles generated using plant extract. An evaluation was performed to assess the antibacterial and antifungal efficacy of the prepared aqueous CABL extract, CABL@AgNPs, and CABL@AuNPs through the implementation of the disc diffusion technique. The results demonstrated that CABL@AgNPs exhibited greater efficiency when compared to both CABL extract and CABL@AuNPs. The dose-dependent nature of antimicrobial activities was clearly demonstrated through the results of antioxidant and anti-inflammatory experiments. The wound healing activity of the prepared nanomaterials was evaluated using a variety of techniques, including MTT assay, fluorescence staining test, and in vitro scratch assay. The wound-healing capacity of prepared nanomaterials was evaluated using an in vitro scratch assay with Fibroblast L929 cells. The impact of nanoparticles at the IC50 concentration range was analysed through a fluorescence staining experiment and MTT assay to determine toxicity levels. The environmentally friendly approach of current study shown that both nanoparticles have the potential to be effective therapeutic agents for treating different illnesses.

Optical characterization and dispersion analyses of plasma polymerized methyl acrylate thin films

This work reports the structural characteristics, surface morphology, linear and nonlinear optical properties of 110 to 225 nm thick plasma polymerized methyl acrylate (PPMA) thin films. X-ray diffraction analyses confirm the amorphous nature of the films. Field emission scanning electron micrographs of the films display cluster-based surface morphology. Attenuated total reflectance Fourier transform infrared spectroscopy confirms the chemical structural changes in the films. The optical properties were studied based on the absorbance, transmittance, and reflectance spectra measured by an ultraviolet–visible spectrophotometer within the wavelength ranges from 200 to 800 nm. The direct optical band gap and Urbach values are increased from 3.66 to 3.83 eV and 0.28 to 0.45 eV, respectively with increasing film thickness. The extinction coefficient and refractive index were evaluated, and discussed a correlation between the refractive index and the optical bandgap. The real and imaginary dielectric constants, volume/surface energy loss functions and skin depth were deduced. The oscillator energies and parameters were analyzed using the concept of Wemple-DiDomenico and Sellmeier models, respectively for a single oscillator. Static linear refractive index for the studied films exhibits normal dispersion behavior with film thicknesses and satisfied Moss, Ravindra-Gupta, and Herve-Vandamme rules. The linear susceptibility, third-order nonlinear susceptibility and the non-linear refractive index are considerably reduced from 0.20, 29.5 × 10−14 esu, and 5.89 × 10−12 esu with increasing optical band gap energies. The outcomes from the analyses of PPMA demonstrated their potential for usage in electronic, optoelectronic, and non-linear device applications.

Exploring the collaborative wonders of Al2O3-Mn3O4-Fe2O3 nanoparticles embedded in reduced graphene oxide matrices

Synergistic nanomaterials with enhanced electrical, magnetic, anticorrosive, and photocatalytic characteristics were synthesized through a controlled hydrothermal process using a reduced graphene oxide matrix for entrapping Al2O3-Mn3O4-Fe2O3 nanoparticles. The structure and properties of the nanocomposites were characterized using X-ray diffraction, Scanning electron microscopy, Ultraviolet–visible spectroscopy, and Fourier transform infrared spectroscopy techniques. The synergistic combination of reduced graphene oxide and ternary metal oxide nanoparticles resulted in enhanced magnetic properties and improved anticorrosive and photocatalytic activity. The photocatalytic activity was tested for the degradation of organic dye (methylene blue) under ultraviolet-A and B lamps. The induced current increased with the strength of the applied magnetic field. The nanocomposites exhibited a paramagnetic character. The photocatalytic properties of the nanocomposites were investigated with time using an ultraviolet–visible spectrophotometer. The nanocomposites degrades 65 % of methylene blue dye in 60 min. of UV light exposure. The nanocomposites show a maximum of 98.24 % corrosion inhibition efficiency for mild steel in 1.0 M H2SO4 medium. These innovative ternary metal oxides embedded in reduced graphene oxide nanocomposites might be used in water purification, environmental remediation, and anticorrosive applications, improving the fields of materials science and nanotechnology.

Green synthesis of silver nanoparticles using Illicium verum extract: Optimization and characterization for biomedical applications

Abstract The synthesis of noble metal nanoparticles is currently experiencing substantial development and considerable attention. Plant extracts are commonly used for the biological synthesis of nanoparticles because they contain biologically active constituents. In our present study, silver nanoparticles (AgNPs) were synthesized using an aqueous Illicium verum (Star anise) extract to evaluate their antimicrobial, antioxidant, and cytotoxicity activities. For maximum yields of AgNPs, the extract (2.5 ml), silver ions (500 µM), and pH (8) were shown to be the ideal nanoparticle production parameters. The visual colour shifted from pale brown to dark brown when the ultraviolet-visible spectrophotometer was used to validate the synthesis of AgNPs. A transmission electron microscope was utilized to evaluate nanoparticles’ physical nature. The presence of silver metal with face-centred cubic symmetry was confirmed by X-ray diffraction analysis. Fourier-transform infrared spectroscopy was used to identify the functional groups in charge of reducing silver ions (Ag+) and the stability of AgNPs produced using the I. verum aqueous extract. The agar well diffusion method investigated the antibacterial activity of I. verum silver nanoparticles (Iv-AgNPs) against pathogenic bacteria and fungi. At higher doses (100 µg·mL−1), the highest zone of inhibition was observed, and spherical AgNPs demonstrated the antibacterial activity. The I. verum extract and Iv-AgNPs enhanced (70%) their free radical scavenging activity at 500 µg·mL−1 according to the 2,2-diphenyl-1-picrylhydrazyl assay. Moreover, the cytotoxicity of Iv-AgNPs against the HCT-116 human colon cancer cell line indicated cell inhibition in a dose-dependent manner. Ultimately, the findings of this study indicate that techniques used to produce AgNPs are environmental friendly, cost-effective, harmless, uncomplicated, and can effectively tackle a broad spectrum of medical and nutritional concerns.

Nuclear radiation shielding performance of the new lead‐free TeO2–Bi2O3–ZnO–BaF2 glass

AbstractThis paper studied the radiation shielding properties of new lead‐free telluride glass with different BaF2 content. The 65TeO2–15Bi2O3–(20 − x)ZnO–xBaF2 glass systems (where x = 1, 3, 5, 7, 9 mol%) were tested through the X‐ray diffraction, ultraviolet–visible spectrophotometer, and differential scanning calorimetry. The glass system exhibited good thermal stability and a uniform surface without surface crystallization. The linear attenuation coefficient of the TBZBF series glass was tested using five different gamma radiation sources (241Am, 133Ba, 57Co, 137Cs, and 60Co). They were calculated to the mass attenuation coefficient, half‐value layer, mean free path, and effective atomic number through numerical simulations with XCOM software. The maximum mass attenuation coefficient for TBZBF‐9 was calculated to be 5.3577 cm2/g. Comparisons were made between this glass system and other tellurite and leaded glasses reported in the literature. The glass system exhibited superior radiation shielding capability compared to leaded tellurite glass under the same testing conditions. The gamma radiation shielding capacity increased with BaF2 content in the glass system. These results show that TBZBF‐9 exhibited the best gamma radiation shielding effectiveness while maintaining glass transparency.

Development of Vitamin C-Loaded Electrospun Nanofibers of Mixture of Polysaccharides of Pullulan/Xanthan Gum for Fast Dissolving Oral Film Applications.

In this study, polysaccharide-based nanofibrous fast dissolving oral films (FDOFs) were developed using pullulan (PUL) and xanthan gum (XG) via electrospinning. The edible, continuous, and bead-free nanofibers with average diameters ranging from 181.17 nm to 260.84 nm were prepared. The morphological, thermal, mechanical, and water-soluble properties of the nanofibrous FDOFs were characterized. For prospective future applications of the developed PUL/XG FDOFs, a model nutrient of vitamin C (VC) was encapsulated into the FDOFs. The success of VC encapsulation was confirmed by Fourier transform infrared spectroscopy. The encapsulation efficiency of VC was above 85% by ultraviolet-visible spectrophotometer. The amorphous structure of PUL/XG in the nanofibers film was demonstrated by X-ray diffractometer. In addition, the edible FDOFs could dissolve in water within 3 s. The nanofibers film we prepared could be used as nutrient or drug carriers and edible packaging film.

Spectroscopic analysis of lead lanthanum zirconate titanate films using UV-VIS and ellipsometry

Spectroscopic ellipsometry and ultraviolet-visible (UV-VIS) spectrometry were utilized to study the optical properties of ferroelectric lead lanthanum zirconate titanate (PLZT) films. These films were deposited on platinized silicon [Si(100)/ SiO2/TiO2/Pt(111)] substrates using the chemical solution deposition method. Films were annealed at two different temperatures (650 and 750 °C) using rapid thermal annealing. Shimadzu UV-1800 UV-VIS spectrophotometer with a resolution of 1 nm was used to measure the reflectance data in the spectral range of 300–1000 nm with a step size of 1 nm. The bandgap values were determined from the reflectance spectra using appropriate equations. A J.A. Woollam RC2 small spot spectroscopic ellipsometer was used to obtain the change in amplitude (Ψ) and phase (Δ) of polarized light upon reflection from the film surface. The spectra were recorded in the wavelength range of 210–1500 nm at an incident angle of 65°. Refractive index (n) and extinction coefficient (k) were obtained by fitting the spectra (Ψ, Δ) with the appropriate models. No significant changes were observed in the optical constants of PLZT films annealed at 650 and 750 °C. The optical transparency and the strong absorption in the ultraviolet (UV) region of PLZT films make them an attractive material for optoelectronic and UV sensing applications.

Green synthesis of zinc oxide nanoparticles using aqueous extract of shilajit and their anticancer activity against HeLa cells

In the present study, ZnO nanoparticles have been synthesized using an aqueous extract of shilajit. The nanoparticles were characterized using different techniques such as UV (ultraviolet–visible spectrophotometer), FTIR (Fourier transform infrared), XRD (X-ray diffraction), particle size analysis, SEM (scanning electron microscope) and EDAX (Energy-dispersive X-ray) analysis. The UV absorption peak at 422.40 nm was observed for ZnO nanoparticles. SEM analysis showed the shape of nanoparticles to be spherical, FTIR spectrum confirmed the presence of zinc atoms, particle size analysis showed the nanoparticle size, EDAX confirmed the purity of ZnO nanoparticles whereas XRD pattern similar to that of JCPDS card for ZnO confirmed the presence of pure ZnO nanoparticles. The in vitro anticancer activity of ZnO nanoparticles against the HeLa cell line showed the IC50 value of 38.60 μg/mL compared to reference standard cisplatin. This finding confirms that ZnO nanoparticles from shilajit extract have potent cytotoxic effect on human cervical cancer cell lines.

Graphene Quantum Dots: Green Synthesis, Characterization, and Antioxidant and Antimicrobial Potential.

Antibiotic resistance is becoming more common, emphasising the demand for novel antibacterial treatments. The current investigation describes the green synthesis of graphene quantum dots (GQDs) using M. indica leaves and characterization via Fourier-transform infrared spectra (FTIR), X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), and ultraviolet-visible (UV-Vis) spectrophotometer. The results showed that GQDs are spherical in shape. In vitro antioxidant and antimicrobial studies indicate that the biological efficacy of synthesized GQDs was higher than the ethanolic leaf extract. GQDs exhibited the highest scavenging efficacy with lowest IC50 (half-maximal inhibitory concentration) value. However, antimicrobial study showed more inhibitory activity of GQDs against all screened microorganisms, i.e., Staphylococcus aureus, Escherichia coli, Bacillus subtilis, and Pseudomonas aeruginosa, and fungi, i.e., Aspergillus niger and Aspergillus flavus. Graphene quantum dots facilitate reactive oxygen species (ROS) which ultimately lead to antioxidant and antibacterial activity. This approach would provide an efficient alternate method for tackling microorganisms.

Plasma-Activated Media Produced by a Microwave-Excited Atmospheric Pressure Plasma Jet Is Effective against Cisplatin-Resistant Human Bladder Cancer Cells In Vitro.

Media exposed to atmospheric pressure plasma (APP) produce reactive oxygen and nitrogen species (RONS), with hydrogen peroxide (H2O2), nitrite (NO2-), and nitrate (NO3-) being among the most detected species due to their relatively long lifetime. In this study, a standardized microwave-excited (ME) APP jet (APPJ) source was employed to produce gaseous RONS to treat liquid samples. The source was a commercially available plasma jet, which generated argon plasma utilizing a coaxial transmission line resonator at the operating frequency of 2.45 GHz. An ultraviolet-visible spectrophotometer was used to measure the concentrations of H2O2 and NO3- in plasma-activated media (PAM). Three different types of media (deionized water, Hank's balanced salt solution, and cell culture solution Dulbecco's modified eagles medium [DMEM]) were utilized as liquid samples. Among these media, the plasma-treated DMEM was observed to have the highest levels of H2O2 and NO3-. Subsequently, the feasibility of using argon ME-APPJ-activated DMEM (PAM) as an adjuvant to enhance the therapeutic effects of cisplatin on human bladder cancer cells (T-24) was investigated. Various cancer cell lines, including T-24 cells, treated with PAM were observed in vitro for changes in cell viability using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay. A viability reduction was detected in the various cancer cells after incubation in PAM. Furthermore, the study's results revealed that PAM was effective against cisplatin-resistant T-24 cells in vitro. In addition, a possible connection between HER expression and cell viability was sketched.

Plasmon-based colorimetric assay using green synthesized gold nanoparticles for the detection of bisphenol A.

Herein, we report a green synthesized gold nanoparticle (AuNPs) based colorimetric detection of bisphenol A (BPA). The AuNPs were synthesized using khat leaf extract as a reducing agent by optimizing factors affecting the AuNPs synthesis, including gold precursor concentration (1mM), and reaction temperature (60°C). The AuNPs characterization was carried out using ultraviolet-visible spectrophotometry and transmission electron microscopy, and it was found spherical with an average particle size of 17.3 ± 3.7nm. A colorimetric nanosensor was developed by conjugation of bio-inspired AuNPs with BPA-specific aptamer for a quick and easy detection of BPA in plastic bottled water. The colorimetric assay relies on the strong affinity of BPA for aptamer, which causes detachment of the aptamer from the AuNPs surface in the presence of BPA inducing AuNPs aggregation. To achieve the colorimetric detection of BPA, the concentrations of NaCl and aptamer were optimized. The detection of BPA was monitored visually using a naked eye, as well as quantitatively using an ultraviolet-visible spectrophotometer. The method visual limit of detection (LOD) was determined to be 0.1ng/mL and reached 0.09ng/mL using ultraviolet-visible spectrophotometer. The method demonstrated very good linearity (R2 = 0.9986) in the range of 0.1-100ng/mL. The proposed method showed high sensitivity to BPA detection in plastic bottled water with 86.7-98.0%, recovery. Therefore, the proposed colorimetric nanosensor can be used for determination of BPA in plastic bottled waters with reliable performance at lower concentrations.

Rapid identification of bacteria in water by multi-wavelength transmittance spectroscopy and the artificial neural network

Background: Multi-wavelength transmittance spectroscopy, in combination with the artificial neural network, has been a novel tool used to identify and classify microorganisms in recent years.Methods: In our work, the transmittance spectra in the region from 200 to 900 nm for four bacterial species of interest, Escherichia coli (E. coli), Staphylococcus aureus (S. aureus), Klebsiella pneumoniae (K.pneumoniae), and Salmonella typhimurium (S. typhi), were recorded using an ultraviolet–visible spectrophotometer. Considering too much redundant data on the full-wave band spectra, the characteristic wavelength variables were selected using the competitive adaptive reweighting sampling (CARS) algorithm. Spectra of the initial training set of these targeted microorganisms were used to create identification models representing the spectral variability of each species using four kinds of neural networks, namely, backpropagation (BP), radial basis function network (RBF), generalized regression neural network (GRNN), and probabilistic neural network (PNN).Results: The blinded isolate spectra of targeted species were identified using the four identification models given above. Compared to fullband modeling, after using CARS to screen the wavelength variables, four identification models are established for the 35 preferred characteristic wavelengths, and the prediction performance of the four models is notably improved. Among them, the CARS–PNN model is the best, and the identification rates of all targeted bacteria were achieved with 100% accuracy; the calculation time is just approximately 0.04 s.Discussion: The use of CARS can effectively remove useless information from the spectra, reduce model complexity, and enhance model prediction performance. Multi-wavelength transmission spectroscopy, combined with the CARS–PNN method, can provide a new method for the rapid detection of bacteria in water and could be readily extended for bacterial microbiological detection in blood and food.

Investigations on the optical, dielectric, electrical, and rheological properties of PEG200/ZnO semiconducting nanofluids for soft matter based technological innovations

Semiconducting nanofluids (SNFs) consisting of poly (ethylene glycol) (PEG200) as a green biocompatible base fluid with homogeneous dispersion of eco-friendly zinc oxide (ZnO) nanomaterial, concentrations ranging from 0.01 to 0.20 wt%, are prepared by state-of-the-art ultrasonic cavitation homogenized process. These PEG200/ZnO SNFs are characterized by employing an ultraviolet-visible (UV-Vis) spectrophotometer, precision inductance-capacitance-resistance (LCR) meter, and rotational viscometer. A detailed analysis of 200–800 nm range UV–Vis absorbance spectra of these SNFs revealed longer stability of suspended ZnO nanoparticles in PEG200 fluid, and their nanomaterial concentrations dependent absorbance and extinction coefficient with tunable dual energy band gaps ranging from 3 to 5 eV. Optical performance recognized the potential applications of these SNFs in the advances of soft matter based optoelectronic and photosensitive devices and also as an excellent UV radiation shielding material. The study of 20 Hz – 1 MHz range dielectric and electrical spectra explained that the ZnO concentrations have a significant impact on the electrical conductivity of these SNFs, while the dielectric permittivity and electrode polarization relaxation process are marginally altered. High static dielectric permittivity (∼ 22) and low electrical conductivity of about μS/cm order, at 303.15 K, evidence the suitability of these SNFs in advances of energy storage devices. The rheological behaviour of PEG200/ZnO materials is carried out at different temperatures ranging from 303.15 to 323.15 K, which illustrates the Newtonian characteristics of these nanofluids with moderate dynamic viscosity and activation energy, and therefore, they could be utilized as effective heat transfer materials in photovoltaic/thermal devices and systems.

Macrofungal Mediated Biosynthesis of Silver Nanoparticles and Evaluation of Its Antibacterial and Wound-Healing Efficacy.

Recently, the utilization of biological agents in the green synthesis of nanoparticles has been given interest. In this study, silver nanoparticles were synthesized from an aqueous extract of macrofungus (mushroom), namely Phellinus adamantinus, in a dark room using 20 µL of silver nitrate. Biosynthesized silver nanoparticles were confirmed by analyzing them using a UV-Vis (ultraviolet-visible) spectrophotometer. The synthesized silver nanoparticles were optimized at different pH and temperatures with various dosages of AgNO3 (silver nitrate) and fungal extracts. The synthesized AgNPs (silver nanoparticles) were characterized using TEM (transmission electron microscopy) and EDX (energy-dispersive X-ray) analyses, which confirmed the presence of silver nanoparticles. The size of the nanosilver particles was found to be 50 nm with higher stability. The mycosynthesized AgNPs showed effective antibacterial activity against strains of Gram-positive (Staphylococcus aureus and Bacillus subtilis) and Gram-negative (E. coli and Pseudomonas aeruginosa) bacteria. The minimum inhibitory concentration (MIC) was found to be 3.125 μg/mL by MIC assay. The MTT assay (3-[4,5-dimethylthiazol-2-yl] 2,5-diphenyl-2H-tetrazolium bromide) was performed to study cytotoxicity, and reduced cell viability was recorded at 100 μg/mL. Silver-Polygalacturonic acid-Polyvinyl alcohol ((Ag-PGA)-PVA) nanofiber was prepared using the electrospinning method. The in vitro wound scratch assay was demonstrated to study the wound-healing efficacy of the prepared nanofiber. The wound-healing efficacy of the AgNP-incorporated nanofiber was found to be 20% after 24 h. This study will lay a platform to establish a unique route to the development of a novel nanobiomaterial and its application in antibacterial and wound-healing therapy.

Characteristics of novel cycloaliphatic epoxides based on UV-induced cationic ring-opening polymerization for plastic coatings

Cationic ring-opening polymerization (CROP)-capable cycloaliphatic epoxide monomers bearing a benzyl ether group (CE-BEs) were developed as glass-replacement plastic coatings for lightweight automobiles. Three different monomers of bis(((7-oxabicyclo[4,1,0]heptan-3-yl)methoxy)methyl)benzene isomers were synthesized to provide the cycloaliphatic epoxide functional groups. 1H and 13C nuclear magnetic resonance and Fourier transform infrared (FT-IR) spectroscopic analyses confirmed that the monomers were successfully synthesized. The shear viscosity and real-time crosslinking behavior of the CROP coatings were investigated using a rheometer. In particular, the release of thermal energy via CROP under UV irradiation was monitored using differential scanning photocalorimetry. The reaction conversion of cycloaliphatic epoxides by CROP before and after UV irradiation was verified using FT-IR spectroscopy. The transparency of the CROP coating films cured on a polycarbonate substrate was measured using an ultraviolet–visible spectrophotometer, and their adhesion was confirmed using cross-cut tests. For characterization of the surface mechanical properties, a nanoindentation tester and a nanoscratch tester were used in conjunction with an atomic force microscope to evaluate the surface hardness and scratch resistance, respectively. In addition, the thermomechanical properties of the cured CROP coating films were investigated using a rigid-body pendulum tester operated in dynamic physical mode. The ternary coating systems with CE-BEs were found to exhibit high photoreactivity, a dense crosslinking density, a transparent appearance, and enhanced adhesion and mechanical properties, making it suitable for glass-replacement plastic coatings.

Investigating the Effect of Ph Variation on the Optoelectronic and Structural Properties of Electrodeposited Copper Selenide Thin Films.

Copper Selenide (CuSe) thin film compound semiconductors have been deposited onto fluorine doped tin oxide (FTO) conducting substrates using electrodeposition technique through various electrolytic bath pH values of 2.00, 2.20, and 2.40. The deposition was carried out in potentiostatic mode using a 2-electrode system set-up at room temperature for 15 minutes at the cathodic voltage of 500 mV. The electrical and the optical properties of the thin films were carried out using photoelectrochemical (PEC) cells and ultraviolet visible spectrophotometer respectively. CuSe thin film possesses a p-type electrical conductivity and the sample grown at semiconductor and a pH of 2.2 was recorded to have the highest PEC signal and highest photo and dark currents that brings forth its maximum power. The energy band gap values of the electrodeposited CuSe thin films were observed to be 2.30 eV, 2.20 eV, and 2.00 eV at bath pH values of 2.0, 2.2, and 2.4 respectively. The optical band obtained at the various pH decreases as pH increases and these band gap values agree with the bulk band gap of CuSe. The preferred orientation peak of electrodeposited CuSe layers exists as klockmannite (CuSe) and the highest peak intensity for the preferred orientation peak occurred at pH of 2.20. At this pH value, the electrodeposited CuSe layers have the highest crystallite sizes.