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Potassium chloride (KCl) nanoparticles were synthesized by ball milling technique with different milling time. The effect of milling time on structural and optical properties was investigated. The structural properties of the purchased samples are characterized by Raman spectroscopy, scanning electron microscope and X-ray diffraction techniques. The Raman spectroscopy of the KCl hints at an excellent alloying behavior of those compounds and a preferred crystal structure for certain composition. The optical band is calculated by analyzing the spectral behavior of the absorption coefficient in the absorption region which revealed direct transitions. The value optical band increases (4.02–5.11 eV) with increasing milling time (0–15 h) due to quantum confinement after the ball milling process. The refractive and absorption indices were calculated for all samples. The model of Wemple–DiDomenico was used to calculate the dispersion parameters. The nonlinear susceptibility of the third order and the nonlinear refractive index were calculated by linear optical parameters using the generalized Miller rule. Mechanical milling for different milling times (0, 5, 10 and 15 h) by a planetary ball mill with zirconium oxide balls has been carried out for milling KCl. The images of as-purchased KCl have regular uniformly grains distributed like cubic particles with size of around 10 μm. By increasing the milling time to 15 h, these individual regular shapes form a smaller reasonably dense having a size less than 500 nm. [ABSTRACT FROM AUTHOR]

Fe3O4 nanoparticles coating with poly dimethyl diallyl ammonium chloride (Fe3O4/PDDA) as novel magnetic adsorbents were synthesized with chemical co-precipitation method to study the removal capacity of organic phosphonates from aqueous solution. The as-prepared magnetic absorbents were characterized for the morphology, material structure and surface properties by SEM, TEM, FT-IR, XRD, TGA and BET. HEDP was employed as a common organic phosphonate to investigate the adsorption performance. Substantial quaternary ammonium groups existing on the surface of Fe3O4/PDDA could enhance the absorption of HEDP with electrostatic attraction. In the optimum condition (4 mg adsorbent dosage, 11.0 pH, 36 mg/L HEDP solution and 120 min adsorption time), the maximum adsorption capacity ( q m ) for HEDP could reach 254.86 mg/g. The kinetic study revealed that the adsorption process followed the pseudo-second-order model. The adsorption isotherm fitted closely to the Freundlich model. The as-prepared magnetic adsorbents exhibited notable reusability in some cycles and were easily separated from the solution with the external magnetic field. These as-prepared Fe3O4/PDDA nanoparticles have the potential as an environmental-friendly adsorbent for organic phosphonates removal from waste-water. Fe3O4 nanoparticles modified with PDDA have been successfully fabricated by the chemical co-precipitation method. The PDDA on the surface of particles provided substantial quaternary ammonium groups which enhanced the absorption of HEDP from aqueous solutions with electrostatic attraction. These magnetic nanoparticles exhibited good reusability in several cycles. [ABSTRACT FROM AUTHOR]

Nanoparticle Lead sulfide was synthesized via simple chemical method and deposited on glass substrates at different substrate temperatures by thermal evaporation technique. The synthesized nanoparticle was analyzed and confirmed by X-ray diffraction (XRD), Scanning electron microscopy SEM with EDX and thermogravimetry. The structural, optical, morphological and electrical properties of the deposited films were studied using XRD, UV-Vis, Raman, SEM with EDX, atomicforce microscopy AFM and Hall Effect measurements. The thickness of the deposited samples was measured using thickness profilometer. The Raman shift in the peak occurs toward lower energy with increasing substrate temperature deposited lead sulfide. The Z-scan study with open aperture was carried out at 532 nm using 5 ns laser pulse on the deposited films which shows that nonlinear absorption arises from saturable absorption process. The deposited film exhibits p-type conductivity in Hall measurement. [ABSTRACT FROM AUTHOR]

Nano nalidixic acid was prepared by ultrasonic method in carbon tetrachloride. Nano nalidixic acid (quinolone antibiotic) was characterized by X-ray diffraction (XRD), infrared spectroscopy (IR) and scanning electron microscope (SEM). The antibacte-rial activities of nano nalidixic acid were tested against microorganisms and compared with the microscale drug. The results show that nano nalidixic acid has good inhibitory properties against two Gram-positive species, Staphylococcus aureus and Bacillus sub-tilis. Nano nalidixic acid also showed good antifungal activity against Candida albicans. Nano nalidixic acid can be injected into the human body as a decontaminating agent to prevent the growth of harmful microorganisms more effectively than the micro-sized drug. [ABSTRACT FROM AUTHOR]

α-Fe2O3 nanoparticles were obtained by a mechanical alloying of micrometer-sized powder at different milling times. Samples were characterized by X-ray powder diffraction, scanning electron microscope (SEM), Mössbauer spectrometry, and vibrating sample magnetometer (VSM). A qualitative and quantitative phase analyses using the Rietveld method have been performed based on the XRD data. The results did not reveal any phase change during the milling. The average particle size decreases with a prolongation of milling times, while the lattice parameters, unit cell volume, and microstrain increase. Mössbauer measurement shows that there are two components, one nanometric and other micrometric. The magnetic hysteresis loops shows that the samples are typical of ferromagnet with superparamagnetic fraction in the material. [ABSTRACT FROM AUTHOR]

Synthesis of uniform nanocrystalline anatase TiO2 by sol–gel method was investigated using different thermal analysis (DTA), thermogravimetric analysis (TGA), X-ray diffraction (XRD) and scanning electron microscope (SEM) techniques. Thermal treatment of the precursor at 350°C for 2 h in air results in the formation of nanocrystalline anatase TiO2 with the average crystal size of 21.5 nm. Quantitative analysis through energy dispersive X-ray spectroscopy (EDS) indicated that the atomic ratio of Ti:O ≈ 1:1 is close to the stoichiometric ratio of TiO2, leading to the evident fact that the prepared nanoparticles are indeed the TiO2 material. [ABSTRACT FROM AUTHOR]