Journal of Metastable and Nanocrystalline Materials
Vol. 30
Vol. 30
Journal of Metastable and Nanocrystalline Materials
Vol. 29
Vol. 29
Journal of Metastable and Nanocrystalline Materials
Vol. 28
Vol. 28
Journal of Metastable and Nanocrystalline Materials
Vol. 27
Vol. 27
Journal of Metastable and Nanocrystalline Materials
Vol. 26
Vol. 26
Journal of Metastable and Nanocrystalline Materials
Vols. 24-25
Vols. 24-25
Journal of Metastable and Nanocrystalline Materials
Vol. 23
Vol. 23
Journal of Metastable and Nanocrystalline Materials
Vol. 22
Vol. 22
Journal of Metastable and Nanocrystalline Materials
Vols. 20-21
Vols. 20-21
Journal of Metastable and Nanocrystalline Materials
Vol. 19
Vol. 19
Journal of Metastable and Nanocrystalline Materials
Vol. 18
Vol. 18
Journal of Metastable and Nanocrystalline Materials
Vol. 17
Vol. 17
Journal of Metastable and Nanocrystalline Materials
Vols. 15-16
Vols. 15-16
Journal of Metastable and Nanocrystalline Materials Vol. 23
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Paper Title Page
Abstract: Nanohybrid thin films consisting of nanocrystalline TiO2 particles in poly(methyl methacrylate)(PMMA) were successfully synthesized by in-situ sol-gel and polymerization assisted by spin coating. Using titanium isoproproxide (Ti-iP), methyl methacrylate (MMA) and 3-(trimethoxysily)propyl methacrylate (MSMA) as the starting materials, nanohybrids containing up to 60% Ti-iP in
PMMA were realized. The resulting nanohybrid thin films coated on quartz substrates are optically transparent and demonstrate nonlinear optical behaviour, where their nonlinear absorption increases with the loading of Ti-iP in PMMA, as confirmed by Z-scan measurements. Using pump-probe technique, these thin films are shown to exhibit an ultrafast relaxation time of ~1.5 picosecond.
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Abstract: The thermooxidative degradation of poly (vinyl alcohol)/silica (PVA/SiO2)
nanocomposite prepared with self-assembly monolayer (SAM) technique is investigated by using a thermogravimetry (TG) and Fourier transform infrared spectroscopy coupled thermogravimetry (FTIR/TG). The results show that although the thermooxidative degradation process of prepared nanocomposite is similar to that of the pure PVA, its thermooxidative stability has been greatly improved.
375
Abstract: A series of partially fluorinated poly(ether imide) (6F-PEI) and (6F-PEI)/Organosoluble MMT clay nanocomposite were synthesized. XRD data, indirectly confirmed the exfoliation of diamine modified MMT clay at molecular level in the nanocomposite. Thermal properties, and longterm thermo-oxidative stability, thermal degradation kinetics, moisture absorption, chemical resistance of (6F-PEI)s, and nanocomposite films were studied and reported in this paper.
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Abstract: Mechanical milling was employed to prepare the nanocomposite precursors for the catalytic growth of carbon nanostructures. For alumina substrates, our study showed that mechanical-millingderived catalyst precursors possessed high hydrogen reduction efficiency that in turn enabled the high yield of CNTs. The alloying effects presented by the mechanical milling could accelerate the
substitutional reactions between the parent oxides and thus the quality of CNTs was apparently improved. In addition, by using water-soluble substrates such as NaCl, we realized large-scale formation of carbon-encapsulated metal nanoparticles (CEMNs) that can be completely separated by a simple washing process. It was found that the morphologies of as-obtained carbon nanostructures were strongly dependent on the substrate effects. By selecting different salt substrates, we can strategically change the morphologies of the as-obtained nanostructures, from CNTs to CEMNs and the intermediate state between CNTs and CEMNs, such as quasi-nanocages.
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Abstract: The carbon microcoils and carbon nanocoils were prepared by the catalytic pyrolysis of acetylene under the Ni and/or Fe-containing catalysts, and the growth pattern, morphology and growth mechanism of the carbon coils were examined in detail. The inner coil diameter of carbon microcoils are of several µm and coil gap from zero to several µm. The inner coil diameter of carbon nanocoils are from zero to several ten nm and coil gap from zero to several nm. The carbon microcoils are
generally of double helix coils such as DNA while carbon nanocoils were single helix coils such as α-helix proteins, with spring-like or twisted forms. A catalyst grain was usually observed on the tip of carbon coil. The carbon nanocoils are almost amorphous and can be graphitized by the high temperature heat-treatment.
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