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This paper presents a green, facile and rapid method to prepare magnetite/zeolite-nanocomposites (NCs) in one step procedure at ambient temperature. The powder X-ray diffraction (PXRD) pattern of iron oxide nanoparticles (NPs) with the sole zeolite showed the broadening of zeolite peaks attributed to the incorporation of Fe 3 O 4 . Field-emission scanning electron microscopy (FESEM) analysis depicted that the Fe 3 O 4 ‒NPs were formed on the surface of porous zeolite framework. Transmission electron microscopy (TEM) analysis displayed the Fe 3 O 4 nanoparticles (NPs) were mostly in spherical shape with a mean diameter and standard deviation of 2.40 ± 0.41 nm. The selected-area electron diffraction (SAED) pattern confirmed the presence of cubic Fe 3 O 4 phase. The vibrating sample magnetometer (VSM) results indicated the as-synthesized sample has a saturation magnetization of around 6.52 emu g −1 . The magnetite/zeolite-NCs can be considered as a low-cost alternative catalyst for oxygen reduction reaction (ORR) process. The electrochemical measurement showed that the performance of magnetite/zeolite-NCs towards the ORR increased as the scan rate increased from 20 mV s −1 to 500 mV s −1 . The ORR is a diffusion-controlled process in the alkaline medium. [ABSTRACT FROM AUTHOR]

The goal of this study was to prepare nanocomposites of rice straw coated with different percentages of Fe3O4 nanoparticles (Fe3O4-NPs) [1.0, 5.0, 10.0, and 20.0 wt. %]. In this process, the size of Fe3O4-NPs changed with varying volumes of NaOH (2M). The Fe3O4-NPs were precipitated with sodium hydroxide from a solution of Fe(II) and (III) chloride in water under ambient conditions and N2 gas by the quick precipitation method using urea as a stabilizer. The rice straw/Fe3O4 nanocomposites (NCs) prepared by this method had magnetic properties in percentages higher than ten (10 wt. %). When the volume of NaOH increased, Fe3O4-NPs with uniform size and better distribution could be prepared, which means that the size of the NPs decreased as the reducing agent was increased. Transmission electron microscopy (TEM) showed that Fe3O4-NPs in rice straw were spherical with diameters from 18.47 to 9.93 nm. The SEM results show that the structure of rice straw underwent no particular change. EDX indicated the presence of Fe3O4- NPs on the surface of rice straw. X-ray powder diffraction (PXRD) indicated that the magnetic Fe3O4-NPs were pure and that the particles were small. The FT-IR results showed that the Fe3O4-NPs were successfully coated on the surface of rice straw. [ABSTRACT FROM AUTHOR]

Small sized magnetite iron oxide nanoparticles (Fe3O4-NPs) with were successfully synthesized on the surface of rice straw using the quick precipitation method in the absence of any heat treatment. Ferric chloride (FeCl3.6H2O), ferrous chloride (FeCl2.4H2O), sodium hydroxide (NaOH) and urea (CH4N2O) were used as Fe3O4-NPs precursors, reducing agent and stabilizer, respectively. The rice straw fibers were dispersed in deionized water, and then urea was added to the suspension, after that ferric and ferrous chloride were added to this mixture and stirred. After the absorption of iron ions on the surface layer of the fibers, the ions were reduced with NaOH by a quick precipitation method. The reaction was carried out under N2 gas. The mean diameter and standard deviation of metal oxide NPs synthesized in rice straw/Fe3O4 nanocomposites (NCs) were 9.93 ± 2.42 nm. The prepared rice straw/Fe3O4-NCS were characterized using powder X-ray diffraction (PXRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy dispersive X-ray fluorescence (EDXF) and Fourier transforms infrared spectroscopy (FT-IR). The rice straw/Fe3O4-NCs prepared by this method have magnetic properties. [ABSTRACT FROM AUTHOR]

In this paper, Polyimide/Montmorillonite Nanocomposites (PI/MMT NCs), based on aromatic diamine (4-Aminophenyl sulfone) (APS) and aromatic dianhydride (3,3',4,4'-benzophenonetetracarboxylic dianhydride) (BTDA) were prepared using in situ polymerization and solution-dispersion techniques. The prepared PI/MMT NCs films were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), transmission electron microscopy (TEM) and thermogravimetric analysis (TGA). The XRD results showed that at the content of 1.0 wt % Organo Montmorillonite (OMMT) for two techniques and 3.0 wt % OMMT for the in situ polymerization technique, the OMMT was well-intercalated, exfoliated and dispersed into polyimide matrix. The OMMT agglomerated when its amount exceeded 10 wt % and 3.0 wt % for solution-dispersion and in situ polymerization techniques respectively. These results were confirmed by the TEM images of the prepared PI/MMT NCs. The TGA thermograms indicated that thermal stability of prepared PI/MMT NCs were increased with the increase of loading that, the effect is higher for the samples prepared by in situ polymerization technique. [ABSTRACT FROM AUTHOR]

A green quick precipitation method was successfully used for synthesis of magnetic iron oxide nanoparticles (Fe3O4-NPs) on the surface of sodium/potassium type zeolite. Ferric chloride, ferrous chloride and sodium hydroxide aqueous solutions were used in the synthesis and coating of the Fe3O4-NPs on the surface of the zeolite to produce the zeolite/magnetic iron oxide nanocomposite (zeolite/Fe3O4 -NCs). The reaction was performed in aqueous suspension phase under the ambient condition as green chemistry method. Characterization with Fourier transforms infrared spectroscopy (FT-IR), powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), energy dispersive X-ray fluorescence (EDXF) and transmission electron microscopy (TEM) confirmed the formation of Fe3O4-NPs with mean particle sizes of 3.55±1.02 nm on the surface of the zeolite. [ABSTRACT FROM AUTHOR]