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Abstract  

In this research, for the first time Nb and Ge were doped into titanosilicate nanoparticles up to 25% simultaneously. Crystalline phases and morphology of the synthesized samples were studied by X-ray diffraction (XRD) method and scanning electron microscope (SEM), respectively. Elemental analysis of the samples was performed using X-ray fluorescence (XRF) and Energy dispersive X-ray (EDX) techniques. Surface area of the samples was measured by BET method. Ion exchange potential of the synthesized samples for Sr2+ and Cs+ and effective parameters such as concentration, temperature, time, and pH were investigated. In addition,137Cs and 90Sr radio nuclides absorption in the best appropriate sample was examined. The selectivity of the samples for absorption of 137Cs and 90Sr was studied by gamma spectroscopy, liquid scintillation spectrometry, and atomic absorption spectroscopy methods. The obtained results showed that the prepared samples had good potential for absorption of 137Cs and 90Sr from the model solution. The sample containing equal amount of niobium and germanium, removed completely the 137Cs within the waste water of Tehran nuclear reactor and 90Sr in the desired solution.

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. R. Sharma 2011 Gadolinium induced fibrosis testing by protein targeting assay and nanoparticles: magnetic resonance microimaging of skin and kidneys J. Walker

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Abstract  

The effect of four nucleating agents on the crystallization of isotactic polypropylene (iPP) was studied by differential scanning calorimetry (DSC) under isothermal and non-isothermal conditions. The nucleating agents are: carbon nanofibers (CNF), carbon nanotubes (CNT), lithium benzoate and dimethyl-benzylidene sorbitol. Avramișs model is used to analyze the isothermal crystallization kinetics of iPP. Based on the increase in crystallization temperature (T c) and the decrease in half-life time (τ½) for crystallization, the most efficient nucleating agents are the CNF and CNT, at concentrations as low as 0.001 mass%. Sorbitol and lithium benzoate show to be less efficient, while the sorbitol needs to be present at concentrations above 0.05 mass% to even act as nucleating agent.

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Abstract  

Nickel ferrite is technologically important magnetic material extensively used in high frequency applications such as microwave device due to its high resistivity and sufficiently low losses. It also finds application in the ferrofluids technology. Therefore, ultrafine nickel ferrite was prepared by autocatalytic combustion of novel nickel ferrous fumarato-hydrazinate precursor. The precursor was characterized by IR, AAS, TG and DTA, and a chemical formula of NiFe2(C4H2O4)3·6N2H4 was fixed. This precursor once ignited with a burning splinter at room temperature, glows and the glow spreads over the entire bulk completing the autocatalytic combustion of the precursor to ultrafine ferrite. The single phase formation of ultrafine nickel ferrite was confirmed by XRD, IR spectra and TEM. The average particle size of the ultrafine ferrite was found to be ∼20 nm by TEM. The observed lower value of saturation magnetization for nickel ferrite was due to the superparamagnetic nature of the particles, which increased with the increasing sintering temperature. The ultrafine nickel ferrite was then sintered at 1000°C for 5 h and was characterized by XRD, IR spectra, SEM and TEM. The variation of resistivity, Seebeck coefficient and a.c. susceptibility as a function of temperature was measured for NiFe2O4 and the results are discussed.

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Summary The paper presents the conditions of synthesis and results in the characterization (chemical analysis, thermal analysis, kinetic of decomposition) for two complex compounds of cadmium: [Cd(S2O3)phen]×H2O and [Cd(S2O3)phen2]×2H2O. The obtained complexes were used as precursors for complex sulfides by controlled thermal decomposition. On the basis of transmission electron microscopy (TEM) the complex sulfides may be included in the nanomaterials category.

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Abstract  

A series of catalysts prepared by dispersing iron oxide on supports of different nature and acidity has been studied. Silica (S) and silica-zirconia mixed oxides (SZ) with different ZrO2 content (from 5 to 45 mass%) were used as supports for the iron oxide phase which was deposited over them by an equilibrium-adsorption method. The red-ox properties of the Fe-catalysts were studied by temperature programmed reduction (TPR) technique. The two well defined and narrow TPR peaks observed could be associated with the reduction steps: I) Fe2O3→FeO and Fe2O3→Fe(0) (at ca. 400°C) and II) FeO→Fe(0) (at ca. 800–900°C). The temperature of the second-step-peak increased with the zirconia content in the support, likely because of the stronger interaction of the iron oxide phase with the support. Activation parameters for the two step-reduction processes were obtained by a simple computation procedure applied to the TPR profiles.

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Abstract  

The crystal structures of BaTiO3 and PbTiO3 fine particles have been investigated by powder diffraction using synchrotron radiation high energy X-rays. It is revealed that a BaTiO3 fine particle essentially consists of tetragonal and cubic structure components at 300 K, whereas a PbTiO3 fine particle consists of a tetragonal structure. Adopting a structure model for the BaTiO3 particle that a cubic shell covers a tetragonal core, the thickness of cubic BaTiO3 shell is estimated at almost constant irrespective of particle sizes. Successive phase transitions are detected in 100 nm particles of BaTiO3 near the phase-transition temperatures of a bulk crystal. The changes in diffraction profiles are small, but they are apparent for a most up-to-date powder diffractometry.

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Abstract  

The thermal decomposition kinetics of nickel ferrite (NiFe2O4) precursor prepared using egg white solution route in dynamical air atmosphere was studied by means of TG with different heating rates. The activation energy (E α) values of one reaction process were estimated using the methods of Flynn–Wall–Ozawa (FWO) and Kissinger–Akahira–Sunose (KAS), which were found to be consistent. The dependent activation energies on extent of conversions of the decomposition reaction indicate “multi-step” processes. XRD, SEM and FTIR showed that the synthesized NiFe2O4 precursor after calcination at 773 K has a pure spinel phase, having particle sizes of ~54 ± 29 nm.

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