862 research outputs found

    Inorganic syntheses assisted by microwave heating

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    This Special Issue on “Inorganic Syntheses Assisted by Microwave Heating” represents one of the few fully dedicated issues on inorganic microwave synthesis published by any international scientific journal and it features five papers and one review article. [...

    Tailoring acidity of HZSM-5 nanoparticles for methyl bromide dehydrobromination by Al and Mg incorporation

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    Three kinds of HZSM-5 nanoparticles with different acidity were tailored by impregnating MgO or varying Si/Al ratios. Both the textural and acidic properties of the as-prepared nanoparticles were characterized by nitrogen adsorption-desorption measurements, X-ray diffraction (XRD), scanning electron microscopy (SEM), ammonia temperature-programmed desorption (NH(3)-TPD) and Fourier transform infrared spectroscopy (FTIR or Py-FTIR). It was found that the intensity of Lewis acid sites with weak strength was enhanced by impregnating MgO or reducing Al concentration, and such an enhancement could be explained by the formation of Mg(OH)(+) or charge unbalance of the MgO framework on the surface of HZSM-5 support. The effect of HZSM-5 nanoparticles' acidity on methyl bromide dehydrobromination as catalyst was evaluated. As the results, MgHZ-360 catalyst with the highest concentration of Lewis acid sites showed excellent stability, which maintained methyl bromide conversion of up 97% in a period of 400 h on stream. Coke characterization by BET measurements and TGA/DTA and GC/MS analysis revealed that polymethylated naphthalenes species were formed outside the channels of the catalyst with higher acid intensity and higher Brønsted acid concentration during the initial period of reaction, while graphitic carbon formed in the channels of catalyst with lower acid intensity and higher Lewis acid concentration during the stable stage

    Ultrafine MnFeO4 powder preparation by combusting the coprecipitate with and without Mg2+ or Zn2+ additives

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    [[abstract]]Ultrafine MnFe2O4 powder with its crystallites less than 100 nm was prepared using a combustion process. The coprecipitates containing the stoichiometric amount of Mn2+ and Fe3+ to form MnFe2O4 were prepared by dissolving the required metallic nitrates in de-ionized water and adding NH4OH to adjust the pH of the solutions to 9. The collected dried precipitates were then heated up to predetermined temperatures and then quickly contacted with the acetone spray. Upon contacting with the heated precipitates, the acetone spray was ignited. The combustion of acetone caused the precipitates to form crystalline MnFe2O4 without chemical segregation. The crystallinity of MnFe2O4 powder so obtained depended on the ignition temperature of acetone spray. MnFe2O4 powder obtained at acetone ignition temperature of 773 K had higher crystallinity than that obtained at acetone ignition temperature of 523 K. The presence of a small amount of Mg2+ or Zn2+ in the composition of the coprecipitates promoted the mobility of constituent ions of the combusted powder and resulted in bigger MnFe2O4 crystallites at a lower acetone ignition temperature.[[incitationindex]]SCI[[incitationindex]]EI[[booktype]]紙本[[booktype]]電子

    On modifying properties of polymeric melts by nanoscopic particles

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    We study geometric and energetic factors that partake in modifying properties of polymeric melts via inserting well-dispersed nanoscopic particles (NP). Model systems are polybutadiene melts including 10-150 atom atomic clusters (0.1-1.5% v/v). We tune interactions between chains and particle by van der Waals terms. Using molecular dynamics we study equilibrium fluctuations and dynamical properties at the interface. Effect of bead size and interaction strength both on volume and volumetric fluctuations is manifested in mechanical properties, quantified here by bulk modulus, K. Tuning NP size and non-bonded interactions results in ~15% enhancement in K by addition of a maximum of 1.5% v/v NP.Comment: 25 pages, 7 figure

    Morphology and Photoluminescence of HfO2Obtained by Microwave-Hydrothermal

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    In this letter, we report on the obtention of hafnium oxide (HfO2) nanostructures by the microwave-hydrothermal method. These nanostructures were analyzed by X-ray diffraction (XRD), field-emission gum scanning electron microscopy (FEG-SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectrometry (EDXS), ultraviolet–visible (UV–vis) spectroscopy, and photoluminescence (PL) measurements. XRD patterns confirmed that this material crystallizes in a monoclinic structure. FEG-SEM and TEM micrographs indicated that the rice-like morphologies were formed due to an increase in the effective collisions between the nanoparticles during the MH processing. The EDXS spectrum was used to verify the chemical compositional of this oxide. UV–vis spectrum revealed that this material have an indirect optical band gap. When excited with 488 nm wavelength at room temperature, the HfO2nanostructures exhibited only one broad PL band with a maximum at around 548 nm (green emission)
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