The detection and measurement of low concentrations of arsenic (V) are the subjects of intense research interest in chemistry and environmental activity. In this research, a polypyrrole-chitosan/cobalt ferrite nanoparticles composite layer was prepared using an electrodeposition method on a gold-coated glass slide. The composite layer was characterized using field emission scanning electron microscopy, energy-dispersed spectroscopy, atomic force microscopy, and a high surface stylus profilometer. The composite layer was used to detect the arsenic in water, and the sensor limitation was about 0.001 ppm. The composite layer was tested using atomic-force microscopy before and after the detection of arsenic. As a result, the roughness was disoriented, as the arsenic was bound on the surface of the composite layer.
SnO2 nanoparticle production using thermal treatment with tin(II) chloride dihydrate and polyvinylpyrrolidone capping agent precursor materials for calcination was investigated. Samples were analyzed using X-ray diffraction (XRD), Scanning Electron Microscopy (SEM), energy dispersive X-ray (EDX), transmission electron microscopy (TEM), Fourier Transform Infrared Spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), diffuse UV-vis reflectance spectra, photoluminescence (PL) spectra and the electron spin resonance (ESR). XRD analysis found tetragonal crystalline structures in the SnO2 nanoparticles generated through calcination. EDX and FT-IR spectroscopy phase analysis verified the derivation of the Sn and O in the SnO2 nanoparticle samples from the precursor materials. An average nanoparticle size of 4–15.5 nm was achieved by increasing calcination temperature from 500 °C to 800 °C, as confirmed through TEM. The valence state and surface composition of the resulting nanoparticle were analyzed using XPS. Diffuse UV-vis reflectance spectra were used to evaluate the optical energy gap using the Kubelka-Munk equation. Greater calcination temperature resulted in the energy band gap falling from 3.90 eV to 3.64 eV. PL spectra indicated a positive relationship between particle size and photoluminescence. Magnetic features were investigated through ESR, which revealed the presence of unpaired electrons. The magnetic field resonance decreases along with an increase of the g-factor value as the calcination temperature increased from 500 °C to 800 °C. Finally, Escherichia coli ATCC 25922 Gram (–ve) and Bacillus subtilis UPMC 1175 Gram (+ve) were used for in vitro evaluation of the tin oxide nanoparticle’s antibacterial activity. This work indicated that the zone of inhibition of 22 mm has good antibacterial activity toward the Gram-positive B. subtilis UPMC 1175.
Ni-Zn ferrite nanoparticles were synthesized via mechanical activation of Zn, NiO and Fe2O3 powders in a high energy planetary ball mill. The 30 h-milled samples in argon, oxygen and air atmospheres were pressed in pellet and toroid shape form and were sintered from 500 °C to 900 °C with 100 °C increments. The X-ray diffraction patterns results indicated a single phase Ni-Zn ferrite formation with a cubic-spinel structure in all the samples sintered at 500 °C. The milling atmosphere had a key role in the synthesis, microstructure and properties of the samples in such a way that this effect sustained even after the completion of sintering process. Thus, the main goal of this study is to scrutinize the effect of sintering temperature in the 30-h-milled samples in different atmospheres on DC electrical resistivity and dielectric behavior of Ni-Zn ferrite samples. The results indicated that although electrical resistivity decreased, dielectric behaviors, i.e. constant, loss and tan increased with increase in sintering temperature. The milled samples in argon had the highest resistivity of 1.2 106 Ωcm at 500 °C, and lowest dielectric constant and loss (4.67 102 and 1.7 at 300 K and frequency 106 MHz, respectively) compared to other samples owing to more homogeneity and smaller average crystallite size, making them a good candidate for high frequency applications. X-ray photoelectron spectroscopy (XPS) revealed the presence of metal ions in their proper valence in the Ni-Zn ferrite crystal structure. Noticeably, a variation in the binding energy for the milled samples in different atmospheres is attributed to the changes in surroundings of Fe3+ and Zn2+/or Ni2+, due to non-equilibrium distribution of cations in tetrahedral and octahedral sites, which is further confirmed by the XRD patterns.
Abstract:A water-based solution of polyvinylpyrrolidone (PVP) at various concentrations and zinc nitrates were used in conjunction with calcination to produce zinc oxide semiconductor nanoparticles. The extent to which the zinc oxide semiconductor nanoparticles had become crystallized was measured using X-ray diffraction (XRD), whilst morphological characteristics were determined using scanning electron microscopy (SEM). Transmission electron microscopy (TEM) supported by XRD results were used to evaluate the average particle size. Fourier transform infrared spectroscopy (FT-IR) was then carried out in order to identify the composition phase, since this suggested that the samples contained metal oxide bands and that all organic compounds had been effectively removed after calcination. A UV-VIS spectrophotometer was used to determine the energy band gap and illustrate optical features. Additionally, photoluminescence (PL) spectra revealed that the intensity of photoluminescence decreased with a decrease in particle size. The obtained results have mainly been inclusive for uses by several semiconductor applications in different fields, such as environmental applications and studies, since an absorption process for energy wavelengths could efficiently occur.
A series of zinc borotellurite glass containing erbium nanoparticles with composition of {[(TeO2)0.70(B2O3)0.30]0.7(ZnO)0.3}1−y(Er2O3)y, y = 0.005, 0.01, 0.02, 0.03, 0.04, 0.05 mole fraction were prepared by using conventional melt-quenching method. The optical properties of the prepared glass samples were measured by using high precision Elipsometer and UV-Vis spectrophotometer. The theoretical analysis for electronic polarizability, oxide ion polarizability and optical basicity were determined by using Lorentz-Lorenz equation on the basis of refractive index and optical band gap energy. It is observed that there is a linear increasing trend of electronic polarizability with increasing content of erbium nanoparticles. The oxide ion polarizability increases with refractive index and decreases with band gap energy. The optical basicity analysis shows that the glass samples possess high basicity.
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