SummaryThis work describes a fast, clean and low-cost approach to synthesize ZnS–PVA nanofluids consisting of ZnS nanoparticles homogeneously distributed in a PVA solution. The ZnS nanoparticles were formed by the electrostatic force between zinc and sulfur ions induced by gamma irradiation at a dose range from 10 to 50 kGy. Several experimental characterizations were conducted to investigate the physical and chemical properties of the samples. Fourier transform infrared spectroscopy (FTIR) was used to determine the chemical structure and bonding conditions of the final products, transmission electron microscopy (TEM) for determining the shape morphology and average particle size, powder X-ray diffraction (XRD) for confirming the formation and crystalline structure of ZnS nanoparticles, UV–visible spectroscopy for measuring the electronic absorption characteristics, transient hot wire (THW) and photoacoustic measurements for measuring the thermal conductivity and thermal effusivity of the samples, from which, for the first time, the values of specific heat and thermal diffusivity of the samples were then calculated.

A new ketene + H2 channel in CH3CHO photolysis is not modelled by quasi-classical trajectories over the transition state.

Gold nanoparticles were prepared in graphene oxide using laser ablation technique. The ablation times were varied from 10 to 40 minutes, and the particle size was decreased from 16.55 nm to 5.18 nm in spherical shape. The nanoparticles were capped with carboxyl and the hydroxyl groups were obtained from Fourier transform infrared spectroscopy. Furthermore, the UV-visible peak shifted with decreasing of nanoparticles size, appearing from 528 nm to 510 nm. The Z-scan technique was used to measure the nonlinear refractive indices of graphene oxide with different concentrations and a gold nanoparticle graphene oxide nanocomposite. Consequently, the optical nonlinear refractive indices of graphene oxide and gold nanoparticle graphene oxide nanocomposite were shifted from1.63×10-9 cm2/W to4.1×10-9 cm2/W and from1.85×10-9 cm2/W to5.8×10-9 cm2/W, respectively.

The present study reports the structural and magnetic characterization of spinel zinc chromite (ZnCr2O4) nanocrystallines synthesized by thermal treatment method. The samples were calcined at different temperatures in the range of 773 to 973 K. Polyvinylpyrrolidone was used to control the agglomeration of the nanoparticles. The average particle size of the synthesized nanocrystals was determined by powder X-ray diffraction which shows that the crystallite size increases from 19 nm at 773 K to 24 nm at 973 K and the result was in good agreement with the transmission electron microscopy images. The elemental composition of the samples was determined by energy dispersed X-ray spectroscopy which confirmed the presence of Zn, Cr, and O in the final products. Fourier transform infrared spectroscopy also confirmed the presence of metal oxide bands for all the samples calcined at different temperature. The band gap energy was calculated from UV-vis reflectance spectra using the Kubelka-Munk function and the band gap energy of the samples was found to decrease from 4.03 eV at 773 K to 3.89 eV at 973 K. The magnetic properties were also demonstrated by electron spin resonance spectroscopy, the presence of unpaired electrons was confirmed, and the resonant magnetic field and theg-factorof the calcined samples were also studied.

Monodispersed spherical CdS nanoparticles embedded into polyvinyl alcohol (PVA) films are synthesized by using an in-situ gamma-irradiation-induced method. The formation mechanism of CdS nanoparticles capped by two united cells of PVA is purposed by means of surrounding the CdS nanoparticles with OH bonds of the PVA chain. CdS nanoparticles are found to possess an unusual orthorhombic structure in monoclinic crystalline PVA. The polymer matrix affords protection from agglomeration and controls the particle size. It is found that the distribution of the prepared nanoparticles increases and a narrower size distribution is observed when the gamma radiation is varied from 10 to 50 kGy. While the average size of the nanoparticles is found to be less affected by the variation of the gamma radiation doses. The size range of the synthesized nanoparticles is 14±1 nm. The optical absorption spectra of synthesized CdS nanoparticles in a polymer matrix reveal the blue shift in the band gap energy with respect to CdS bulk materials owing to quantum confinement effect. The photoluminescence study of nanocomposite films shows the green emission arising from the crystalline defects.

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Silver/polyvinyl alcohol (PVA) nanocomposites are prepared via quick precipitation method, using hydrazine as a reducing agent. Preparing of silver/PVA nanocomposites by this method is done for the first time. The samples are characterized by Uv-Visible spectroscopy, X-ray diffraction (XRD), transmission electron microscopy (TEM). Nonlinear optical properties are carried out by Z-scan technique using a blue CW laser beam operated at wavelength 405 nm. It is shown that the synthesized samples have negative nonlinear refractive index and the magnitude is in the order of 10 −8 . The nonlinear refractive index increases as amount of reducing agent increases.

Nickel nanoparticles were dispersed uniformly in a graphene oxide solution, using a laser ablation technique with different ablation times that ranged from 5 to 20 minutes. The results indicate that the nickel nanoparticle sizes inside the graphene oxide decreased, and the volume fraction for the nickel nanoparticles in the graphene oxide increased with an increasing ablation time. Further, using Fourier Transform Infrared Spectroscopy, the nickel nanoparticles in the graphene oxide demonstrate greater stability from possible agglomeration when the nanoparticle was capped with oxygen from the carboxyl group of the graphene oxide. The thermal effusivity of the graphene oxide and nickel nanoparticle graphene oxide composite was measured using a photoacoustic technique. The concentration of graphene oxide shifted from 0.05 mg/L to 2 mg/L, and the thermal effusivity increased from 0.153 W·s1/2·cm−2·K−1to 0.326 W·s1/2·cm−2·K−1. In addition, the thermal effusivity of the nickel nanoparticles graphene oxide composite increased with an increase in the volume fraction of nickel nanoparticles from 0.1612 W·s1/2·cm−2·K−1to 0.228 W·s1/2·cm−2·K−1.