In this paper, wollastonite glass-ceramics and composites of wollastonite glass– ceramics with 2.5, 5, 10 and 20 weight percent alumina with an average size of 2 microns and also wollastonite glass-ceramics with 2.5, 5, and 10 percent alumina with an average size of 40 nanometers were produced without pressure by Sintering and their physical properties (e.g. bulky density, the percentage of linear shrinkage and relative density) were measured. Sinter operation in the temperature range of 1030-1170 °С was performed for 3 hours. Existing phases in composites by X-ray Diffraction (XRD) and their structure were examined by Scanning Electron Microscopy (SEM) and while measuring mechanical properties of composites such as flexural strength, hardness and compared fracture toughness with base glass ceramic was performed. Results indicate that adding 2.5 percent micron-sized alumina to wollastonite glass-ceramics decreases the flexural strength from 8.01±120 to 10.26±50 MPa and its fracture toughness declines to 0.8±0.74, while by adding 2.5 percent nano-alumina to wollastonite glass – ceramics, the flexural strength increases from 8.01±120 to 20.7±133 MPa and its fracture toughness improves up to 1.40±10. Manuscript profile

In this study, we have synthesized nano Aluminum Fluoride (nAF) nanoparticles by the sol-gel method and studied the nano-sized morphology of crystals. In the other section, the PVC/NiAl2O3/AlF3 (nPNA) nanocomposite was successfully prepared and characterized by FT-IR, and HRTEM techniques. FTIR peaks of the PVC and nPNA have been shown spherical shape of PVC and also spherical shapes nanoparticles of nPNA loaded on PVC. A solvothermal method has been successfully introduced and applied for catalyst efficiency. This nanocomposite was used for the removal of Congo red dye. For this purpose, the morphology and the structure of crystals have been changed by modification on precursor gel. Meanwhile, precursor gel preparation and the interaction on the nano-sized area have been studied. This study exhibited that PVC/NiAl2O3/AlF3 (nPNA) nanocomposite is an effective catalyst for the synthesis of some organic derivatives. The results show that the as-prepared nanocomposite is an efficient catalyst and that PVC/NiAl2O4/AlF3 nanocomposite can be used in the next-generation of some organic reactions and faster production of various materials. Manuscript profile

In this study, nanometer sized of Ag/Fe3O4 nanocomposite (AFN) have been synthesized by using a simple and based on chemical reduction method. The size and shape of (AFN) controlled by using of condensation (Fe2O3 (2.975 mmol), NaBH4 (21.25 mmol), AgNO3 (2.532 mmol) and polyvinylpyrrolidone (PVP) (8.925 mmol K30 Mr=10.000) in 40 ºC. The synthesized AFN was characterized by XRD, scanning electron microscopy (SEM), transmission electron microscopy (TEM) and electron diffraction X-ray (EDX) spectral techniques. Measurements of X-ray diffraction (XRD) confirm that Ag/Fe3O4 nanocomposite have the crystalline structure. The scanning electron microscopy (SEM) images of the as-deposited Ag/Fe3O4 nanocomposite (AFN) have been shown that the particles aggregate into an organized spherical structure, which is characterized by diameter of 10-20 nm. This type of porous aggregate is characterized by large surface area, which could have potential applications in the areas of catalysis and filtration. The population distribution as measured from the TEM images shows the average particle size for the AFN nanocomposite is 10-20 nm. Manuscript profile

The aim of the present study was to develop synthesize, characterize, and find many applications of functionalized metal oxide nanoparticles. Herein, a new strategy is developed to functionalize magnetite nanoparticles to improve their performances of cerium oxide-functionalized Fe3O4@SiO2@CeO2 magnetic nanoparticles (FSC). In this study, after preparing optimized FSC, characterization and identification of their chemical structure were carried out by FT-IR, FESEM, VSM, TGA, DLS, and XRD. Afterward, the functionalized nanoparticles were examined in the delivery of celecoxib as an active drug model involving cerium oxide and hydroxyl functional groups. The results with respect to particle size, present investigation indicate that the formulations (mFSC=5 mg, pH=3.3) can be considered as best among various formulations. Dynamic light scattering (DLS) techniques used to measure particle size and zeta potential distribution revealed successful preparation of an Fe3O4@SiO2@CeO2 nanocomposite prepared on Fe3O4@SiO2 (FS), with a hydrodynamic size distribution of 45 nm. Manuscript profile

One plant seed extract (Psidium guajava) was screened for their bioreduction behavior for synthesis of silver nanoparticles. Psidium guajava (PG) was found to exhibit the good reducing and protecting action in terms of synthesis rate and monodispersity of the prepared silver nanoparticles. UV–visible spectroscopy, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), scanning electron microscopy (SEM), and X-ray energy dispersive spectrophotometer (EDAX) was performed to ascertain the formation of Ag-NPs. Our measurements indicate that biosynthesis of Ag nanoparticles by Psidium guajava (PG) produces Ag nanoparticles with the diameters in the range of 30-36 nm. XRD studies reveal a high degree of crystallinity and monophasic Ag nanoparticles of facecentered cubic (FCC) structure. The FTIR result clearly showed that the extracts containing OH as a functional group act in capping the nanoparticles synthesis. Antibacterial activities of Ag-NPs were tested against the growth of Gram-positive (S. aureus) using SEM. The inhibition was observed in the Ag-NPs against S. aureus. The results suggest that the synthesized Ag-NPs act as an effective antibacterial agent. It is confirmed that Ag-NPs are capable of rendering high antibacterial efficacy and hence has a great potential in the preparation of drugs used againstbacterial diseases. Manuscript profile

White rice husk ash (RHA), an agricultural waste, was used as a silica source forMTW zeolite synthesis. The RHA-MTW zeolite derived from RHA was preparedby hydrothermal method at 150 °C in the presence of tetraethylammoniumhydroxide. ZnO nanoparticles (NPs) were grown in zeolite substrates using asolid state reaction. The synthesized nanocomposite (NC) was characterized byXRD, SEM, DRS and TEM and tested as photocatalytic degradation of methyleneblue (MB) dye from aqueous solution under ultraviolet (UV) light. The BET resultsindicated that pore volume and surface area of ZnO/RHA-MTW NC was smallerthan RHA-MTW zeolite. On the basis of the obtained experimental results, it wasfound that zinc oxide NPs were encapsulated into the channels of RHA-MTWzeolite. The SEM and TEM images of ZnO/RHA-MTW NC confirmed the formationof RHA-MTW particles with size diameter of 2.5 μm and locating of zinc oxideNPs in channels of zeolite with an average size of between 35 nm. The resultsshowed MB degradation had reached 85 % under UV light. The MB indicatedmaximum adsorption at pH=9. The photocatalytic activity of ZnO was enhancedin the presence of zeolite due to reduction of recombination rate of the electroholein ZnO semiconductor.ARTICLE INF O Manuscript profile