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Investigation the structural and magnetic properties of nanocrystalline Co₇₈Zr₁₇B₂Si₁W₂ alloy during melt spinning and annealing processes were the main goal of this study. In this regard, samples were prepared using vacuum induction melting, melt spinning and subsequent annealing. The specimens were evaluated using X-ray diffraction (XRD), field emission scanning electron microscope (FESEM), differential scanning calorimetry (DSC) and vibrating sample magnetometer (VSM). Based on results, nanocrystalline Co₅Zr single phase with hard magnetic properties (Ms=29.5 emu/g and Hc=2.7 kOe) successfully formed during melt spinning process (at wheel speed of 40 m.s^-1). The coercivity value of rapid solidified sample increased to about 3.2 kOe during annealing process up to 400°C. However, more increasing in annealing temperature lead to the transformation of non-equilibrium magnetic Co₅Zr phase to stable Zr₂Co₁₁ phase, which has distractive effects on final magnetic properties.
 

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We report a simple and practical approach for the easy production of superhydrophobic coatings based on TiO₂-SiO₂@PDMS. In this study, we used tetraethylorthosilicate (TEOS) and titanium tetraisopropoxide (TTIP) as a precursor for the sol-gel synthesis of SiO₂ and TiO₂, respectively. Afterward, the surface of nanoparticles was modified by 1,1,1,3,3,3-hexamethyldisilazane (HMDS) before being combined with polydimethylsiloxane (PDMS). The hydrophobic property of coatings was evaluated by static contact angle measurements. The phase composition and structural evolution of the coatings were examined by X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR) analysis. It was shown that changing the weight ratio of the solution composition of the coating can affect the hydrophobicity of the surface. The best sample has shown a superhydrophobic property with a 153˚ contact angle which contained (75%TiO₂-25%SiO₂) and PDMS at a weight ratio of 1:1. Moreover, the results showed that the superhydrophobic coating retains its hydrophobic properties up to a temperature of 450 ˚C, and at higher temperatures, it converts to a super hydrophilic with a water contact angle close to 0 ˚. The SiO₂-TiO₂@PDMS coating degrades methylene blue by about 55% and was shown to be capable of photocatalytically decomposing organic pollutants.

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Graphene Nanoparticles (GNPs), an upshot of nanotechnology have attracted great interest in diverse research fields including dentistry for their unique properties. Graphene Nanoparticles are cytocompatible and when combined with other compounds, they possess improved synergistic antimicrobial and anti-adherence properties against oral pathogens. The cytotoxicity of graphene in the oral setting has been reported to be very limited in the scientific literature. Current applications of graphene include reinforcing Polymethylmethacrylate (PMMA) for the fabrication of dentures, improving properties of dental luting agents like glass ionomer cement, reinforcing restorative composites and ceramics, and improving osseointegration of titanium dental implants by coating with graphene. This paper reviews the nanoparticle ‘Graphene’ and its potential uses in the field of restorative dentistry.
 

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Microstructure evolution and mechanical properties of Zn-22Al alloy after post-ECAP natural/artificial aging were investigated. A homogenization treatment was applied to the casting samples. In addition, after preparing the samples for the ECAP, secondary homogenization treatment was done and then the samples quenched in the water to form a fine grain structure. After 8 passes of ECAP, some ECAPed samples were naturally aged and some ECAPed samples were artificially aged. Natural aging after 8 passes of ECAP showed that Zn-22Al alloy has a quasi-stable microstructure because limited grain growth occurred. Two-phase structure of Zn-22Al alloy prevented excessive grain growth after natural aging. On the other hand, artificial aging after 8 passes of ECAP caused a relatively much grain growth took place. In shorter times of artificial aging, the grain growth rate is faster due to the high surface energy of grain boundaries. On the contrary, as the time of artificial aging increased, the surface energy of grain boundaries decreased, which leads to a decrease in the grain growth rate. In addition, texture evolution was studied after aging artificial. Therefore, the main texture of α and η phases was determined.
 

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In the present investigation, an attempt was made to evaluate the dissolution behavior of Ti in molten KCl-LiCl. The X-ray diffraction (XRD) pattern of heated Ti plate at 800 oC for 4 h without carbon black in molten salt revealed that TiCl3 formation was feasible. For more assurance, Ti plate was heated at 950 oC for 4 h in the presence of carbon black to identify synthesized TiC. Transmission electron microscope (TEM) and scanning electron microscope (SEM) images from precursors and the final product showed that nano-crystalline TiC formation from coarse Ti particles was almost impossible without Ti dissolution. Thermodynamics calculations using Factsage software proved that it was possible to form various TiClx compounds. The TiC formation mechanism can be discussed in two possible ways: a reaction between Ti ion and carbon black for synthesizing TiC (direct) and a reaction between TiCl4 and carbon black led to indirect TiC synthesis. Elemental mapping using energy dispersive X-ray spectroscope (EDS) indicated that up to 815 oC, chlorine existed in the map. 

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Deformation-induced α΄-martensite generally forms at shear bands in the coarse-grained austenite, while it nucleates at grain boundaries in the ultrafine-grained (UFG) austenite. The available kinetics models are related to the nucleation on the shear band intersections, and hence, their application to investigating the kinetics of α΄-martensite formation for the UFG regime cannot be justified. Accordingly, in the present work, the general Johnson–Mehl–Avrami–Kolmogorov (JMAK-type) model was implemented for comparing the kinetics of α΄-martensite formation in the UFG and coarse-grained regimes using an AISI 304L stainless steel. On the experimental front, the X-ray diffraction (XRD) patterns and the electron backscattered diffraction (EBSD) maps were used for phase and microstructural analyses, respectively. It was revealed that the simple JMAK-type model, by considering the dependency of the volume fraction of α΄-martensite on the strain, is useful for modeling the experimental data, predicting the nucleation sites based on the theoretical Avrami exponents, and characterizing the transformation kinetics at low and high strains.

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The growth of industries, populations, and industrial activities includes environmental pollutants. Pollution causes problems such as reduced light transmission, anaerobic conditions, and complications such as allergies and cancer for humans and other living organisms. The adsorption method is one of the most attractive, and efficient methods for removing environmental pollutants such as pharmaceuticals. Among the standard methods for wastewater treatment, adsorption is more efficient than other methods and is more economical. They have a meager price. Adsorption of pollutants can be an excellent way to remove toxic substances from polluted waters and industrial effluents. In this review, pharmaceutical removal by adsorption process was reviewed in details.

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Two-dimensional molybdenum disulfide (MoS₂) is used as a promising flame retardant and smoke suppressant nano additive in polymer composites due to its high thermal stability and layered structure. In this study, thermoplastic polyurethane (TPU) was melt-blended with MoS2 (1wt. %) and a halogen-free intumescent flame retardant (IFR) system. The IFR system consisted of ammonium polyphosphate (APP), Melamine polyphosphate (MPP), and pentaerythritol (PER), with a total amount of 25 wt. %. The TPU/IFR/MoS2 composite exhibited outstanding flame-retardant properties, achieving a UL-94 V-0 rating and a limiting oxygen index (LOI) value of 34%. Reaction-to-fire performance of the TPU/IFR/MoS2 composite was evaluated by cone calorimeter test (CCT). The CCT results indicated high flame-retardant efficiency and considerable smoke suppression performance, along with a significant decrease in the peak heat release rate (PHRR: 65.9%), peak smoke production rate (PSPR: 65.6%), and peak CO production (PCOP: 60.7%) compared to the neat TPU. The significant improvement in fire performance of TPU composite was mainly attributed to the effects of the physical barrier of MoS2 and catalytic carbonization of the IFR system. These resulted in forming an intumescent compact carbonized layer during the combustion, effectively restricting dripping. The continuous structure of the residual char was revealed by FESEM. Thermogravimetric analysis (TGA) indicated improved thermal behavior of the TPU composite in high temperatures. This work provides an effective method to improve the reaction to fire of TPU composites by incorporating traditional IFRs and MoS2, resulting in enhanced fire safety.

 
 

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The trimanganese tetraoxide (Mn₃O₄) nanostructured thin films doped with 2 mol % of nickel (Ni) and molybdenum (Mo) ions were deposited by a simple electrophoretic deposition technique. The structural, optical, and morphological studies of these doped thin films were compared with pure Mn₃O₄ thin films. X-ray diffraction (XRD) confirmed the tetragonal Hausmannite spinel structure. The Fourier transform infrared spectroscopy (FTIR) provided information about the molecular composition of the thin films and the presence of specific chemical bonds. The optical study and band gap energy values of all thin films were evaluated by the UV visible spectroscopy technique. The scanning electron microscopy (SEM) illustrated the morphological modifications of the Mn₃O₄ thin films due to doping of the nickel and molybdenum ions. The Brunauer Emmett Teller (BET) method has confirmed the mesoporous nanostructure and nanopores of the thin films. The supercapacitive performance of the thin films was studied by cyclic voltammetry (CV), and galvanostatic charge discharge (GCD) techniques using the three-electrode arrangement. An aqueous 1M Na₂SO₄ electrolyte was used for the electrochemical study. The 2 mol % Ni doped Mn₃O₄ thin film has shown maximum specific capacitance than pure and Mo doped Mn₃O₄ thin films. Hence, this study proved the validity of the strategy - metal ion doping of Mn₃O₄ thin films to develop it as a potential candidate for electrode material in the futuristic energy storage and transportation devices.

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In this research work, Cadmium Sulphide thin film deposited on to glass substrate in a non-aqueous medium at 80 °C. The various physical preparative parameters and the deposition conditions, such as the deposition time and temperature, concentrations of the chemical species, pH, speed of mechanical stirring, etc., were optimized to yield good quality films. The as-prepared sample is tightly adherent to the substrate's support, less smooth, diffusely reflecting and was analyzed for composition. The synthesized film is characterized using X- ray diffraction (XRD), electrical and optical properties. It appears that the composites are rich in Cd. The grown CdS thin film had an orange-red color. A band gap of CdS thin film is 2.41 eV.  The average crystallite size of the CdS film was 21.50 nm. The resistivity of the CdS thin film is about 5.212 x 10⁵ W cm.
 

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Iron oxide nanoparticles has attracted extensively due to their supermagnetic properties, preferred in biomedicine because of their biocompatibility and potential nontoxicity to human beings. Synthesis of iron nanoparticles (FeNPs) was prepared with the help of ferric chloride and ferrous sulphate by using the coprecipitation method. The variation and combination of ferric and ferrous concentrations affect the physical and magnetic properties of iron oxide nanoparticles.  The effect of 0.1 M ferric and ferrous concentration on iron oxide nanoparticles studied separately and in combination. The obtained nanoparticles were characterized by Particle size, zeta potential, Ultraviolet (UV-visible), Fourier Transform Infrared Spectroscopy (FTIR), X-ray diffraction (XRD), Scanning electron microscope (SEM), Thermal gravimetric analysis (TGA), and Vibrating-sample magnetometer (VSM) techniques. Particle size was below 200nm and zeta potential was within the limit for all the batches. UV visible spectra at 224 nm, and FTIR exhibit two peaks at 510 and 594 cm-1, indicating iron oxide NPs and XRD confirmed the crystalline nature of Fe. SEM showed a spherical shape for all batches. The use of a combination of ferric and ferrous is more effective than its individual use. TGA and VSM studies confirmed its magnetic properties.
 

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Drug-resistance among bacteria is a concerning issue in medical field. Silver nanoparticles (AgNPs) are one of the promising novel nano-antibiotics. In the present study, AgNPs were synthesized using cell-free extract of Acinetobacter sp. challenged with silver nitrate. Preliminary observations done using UV-Vis spectrophotometry at 420 nm. Complete reduction of silver ions to AgNPs was confirmed through cyclic voltammetry. Electron microscopy revealed formation of spherical shaped nanoparticles of size upto 20 nm. These AgNPs were furthr used to determine their effect on activity of various antibiotics against pathogenic bacteria such as Neisseria and Xanthomonas. Higher antibacterial activity of AgNPs was observed against Gram-negative bacteria. Enhanced antibacterial action of AgNPs was observed with selected beta-lactam antibiotics producing upto 3-fold increase in area of zone of inhibition. On exposure to AgNPs, the minimum inhibitory concentration and minimum bactericidal concentration of antibiotics were lowered by upto 2000 times indicating potential synergistic action of AgNPs. This study clearly signifies that the drug, proved to be inefficient due to bacterial resistance, could be made functional again in presence of AgNPs. This will help in development of novel antibacterial formulations containing antibiotics and nanoparticles to combat multiple drug-resistance in microorganisms.

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The Mn-Zn ferrite with a composition of Mn_0.25Mg_0.08Cu_0.25Zn_0.42Fe₂O₄ has been synthesized in this study using the chemical sol-gel technique at a pH of 7. The sample was prepared and subsequently annealed at a temperature of 700°C. The nanocrystalline ferrite samples were subjected to characterization using X-ray diffraction (XRD), Fourier transform-infrared spectroscopy (FT-IR), Scanning electron microscopy (SEM), Thermogravimetry (TG), and Differential thermal analysis (DTA). The findings of these observations are delineated and deliberated. The sample's phase composition was verified using X-ray diffraction examination. The crystalline size was determined using Scherrer's formula and was observed to be within the range of 20-75 nm. Two notable stretching bands were seen in the FTIR spectra within the range of 400-650 cm^-1. The spinel structure of the produced nanoparticles was confirmed by these two bands. The magnetic characteristics of the powder were examined using a Vibrating Sample Magnetometer (VSM). The presence of M-H hysteresis loops suggests that the produced nanoparticles have superparamagnetic properties, as evidenced by their low coercive force, remanent magnetization, and saturation magnetization values.
 

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We have modeled theoretical incident photon-to-current electricity (IPCE) action spectra of poly(3-hexylthiophene) (P3HT) and [6,6]-Phenyl C61 butyric acid methyl ester active layer bulk-heterojunction. By the two-dimensional optical model of a multilayer system based on the structure of Glass substrate / SiO₂ /ITO/ PEDOT: PSS /P3HT: PCBM(1:1)/Ca/Al, the optical responses of the device have been computed for different photoactive layer and Ca layer thicknesses to found an optimal structure which allows obtaining the maximum absorption localized in the active layer and high device performance. The electric field intensity, energy dissipation, generation rate, and IPCE have been computed to enhance the device's performance. The finite element method executes the simulation under an incident intensity of 100 mW/cm² of the 1.5 AM illumination. It was found that the optimum structure is achieved by a 180 nm photoactive layer and 5 nm Ca layer thicknesses.

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Researchers are increasingly focusing on green synthesis methods for silver nanoparticles due to their cost-effectiveness and reduced environmental impact. In this study, we utilized an edible bird's nest (EBN), a valuable economic resource, as the primary material for synthesizing silver nanoparticles using only water as the solvent. Metabolite profiling of the EBN extract was conducted using LC-QTOF-MS in positive mode (ESI+), revealing the presence of lipids, glycosides, peptides, polysaccharides, and disaccharides. Upon the addition of silver nitrate to the aqueous EBN extract, noticeable color changes from transparent to brown indicated the successful formation of AgNPs. Subsequent characterization of these silver nanoparticles involved UV-Visible spectroscopy, which revealed an absorption peak at 421 nm. Further characterization was carried out using FESEM, ATR-FTIR spectroscopy, and EDX analysis. The involvement of phenolic agents, proteins, and amino acids in reducing the silver particles was confirmed. The synthesized nanoparticles exhibited a spherical shape, and a particle size ranging from 10 to 20 nm. The presence of elemental silver was confirmed by a strong, intense peak around 3 keV in the EDX spectrum. To assess their potential, the antibacterial properties of the silver nanoparticles against Escherichia coli and Staphylococcus aureus were evaluated using the agar diffusion method.
 

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Acrylic resins are one of the most important thermoplastic resins used in various industries due to their significant properties. However, they are inherently brittle and addition plasticizers to them is very common. In this study, role of both Polyethylene Glycol (PEG) and Triacetin on the mechanical properties of acrylic resin have been investigated. To do so tensile test, bending and wear tests have been performed. To achieve the optimal mixture of plasticizers, a tensile test has been carried out, and the best percentage of the mixture has been determined. Subsequently, bending and wear tests were conducted, which showed a significant increase in the bending strength of the acrylic resin after the addition of plasticizers. Furthermore, it was found that the abrasion mechanism of the resin was significantly altered compared to its pure state.
 

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Rice husk carbon by-product from the industrial combustion is a promising source to produce a vast amount of activated carbon adsorbent. This research prepared rice husk-activated carbon adsorbent by varying the concentration of potassium hydroxide solution (5, 10, 15, 20 % w/v) and activation time (2, 4, 6, 8 hours). Fourier-transform infrared spectral characterization (FTIR) indicated a significant effect before and after activation, especially the presence of hydroxyl groups. Based on the iodine adsorption, the specific surface area of the produced-activated carbon was approximately 615 m²/g. Experimental results showed that increasing potassium hydroxide concentration and activation time increases the water vapor adsorption capacity of the activated carbon. Compared with the rice husk carbon, the KOH-activated carbon enhanced the water vapor adsorption capacity to 931%. In the adsorption observation, changing the temperature from 15 to 27 ℃ caused a higher water vapor uptake onto the activated carbon. Two adsorption kinetics (pseudo-first- and pseudo-second-order models) were used to evaluate the adsorption mechanism. This research found that rice husk-activated carbon performed a higher water vapor adsorption capacity than other adsorbents (silica gel, zeolite, and commercially activated carbon).

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Biogenic synthesis of papain-conjugated copper metallic Nanoparticles and their antibacterial and antifungal activities Papain metallic conjugated nanoparticles (Papain-CuNPs) were synthesised using Papain and CuSO4.5H₂O. Papain-CuNPs were characterized using UV-visible spectroscopy, FT-IR, HR-TEM, XRD, FE-SEM, zeta potential, and a zeta sizer. The antibacterial activity of papain-CuNPs against human infectious microorganisms (Citrobacter spp, Pseudomonas aeruginosa and Candida albicans) was investigated. The mechanism of action of papain-CuNPs was evaluated using FE-SEM and HRTM. UV spectroscopy confirmed the plasma resonance (SPR) at 679 nm, which indicated the formation of papain-CuNPs. The FT-IR spectrum absorbance peaks at 3927, 3865, 3842, 3363, 2978, and 2900 cm^-1 indicate the presence of O-H and N-H of the secondary amine, and peaks at 1643 and 1572 cm^-1 represent C=O functional groups in Papain-CuNPs. EDAX analysis confirmed the presence of copper in the papain-CuNPs. The zeta potential (-42.6 mV) and zeta size (99.66 d. nm) confirmed the stability and size of the nanoparticles. XRD confirmed the crystalline nature of the papain-CuNPs. FE-SEM and HRTM showed an oval structure, and the nano particles' 16.71244–34.84793 nm. The synthesized papain-NPs showed significant antibacterial activity against clinical P. aeruginosa (15 mm). MIC 125 µg/ml) showed bactericidal activity against P. aeruginosa and the mechanism of action of Papain-NPs was confirmed using an electron microscope by observing cell damage and cell shrinking. Papain-CuNPs have significant antibacterial activity and are thus used in the treatment of P. aeruginosa infections

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High entropy intermetallic compounds (HEICs) are an interesting class of materials combining the properties of multicomponent solid solutions and the ordered superlattices in a single material. In this work, microstructural and magnetic properties of (CoCuFeMnNi)Al, (CoCuFeMnNi)Zn₃, (FeCoMnNiCr)₃Sn₂, (FeCoNiMn)₃Sn₂ and Cu₃(InSnSbGaGe) HEICs fabricated by induction melting are studied. The magnetic properties of the HEICs was determined mainly by the nature of the magnetic momentum of the constituent elements. (CoCuFeMnNi)Al and (CoCuFeMnNi)Zn₃ displayed ferromagnetic behavior at 5 K, while indicated linear dependency of magnetization vs. magnetic (i.e. paramagnetic or antiferromagnetic state) at 300 K. The magnetization of (FeCoMnNiCr)₃Sn₂, (FeCoNiMn)₃Sn₂ and Cu₃(InSnSbGaGe) HEICs at 300 K exhibited a nearly linear dependency to magnetic field. Among all the investigated samples, (CoCuFeMnNi)Al exhibited the best magnetic properties with a saturation magnetization of about Ms = 6.5 emu/g and a coercivity of about H_c = 100 Oe.

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The composite solid polymer electrolyte films were prepared by doping nano-sized Fe₂O₃ particles on PVB (Polyvinyl Butyral) complexed with NaNO₃ salt by solution casting technique. FTIR, XRD, and SEM methods characterized these electrolyte films. The Fourier Transform Infrared Spectroscopy and X-ray diffraction methods reveal the structural and complexation changes occurring in the electrolytes. The surface morphology of the electrolyte film was examined using the SEM (Scanning Electron Microscope) technique. The PVB+NaNO₃+Fe₂O₃(70:30:3%) electrolyte shows a moderate ionic conductivity of 2.51×10⁻⁵ S cm⁻¹ at ambient temperature (303 K). AC impedance spectroscopic analysis evaluates the ionic conductivity of the produced polymer electrolyte. Wagner's polarisation technique was applied to study the charge transport characteristics in the electrolyte films. The investigation revealed that ions constituted the majority of the transport carriers. An Open Circuit Voltage (OCV) of 2.0V and a Short Circuit Current (SCC) of 0.8 mA were found in the discharge characteristics data for the cell constructed with the polymer electrolyte sample.