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High-resolution Scanning Electron Microscopy (high-resolution + scanning_electron_microscopy)
Selected AbstractsTowards correlative imaging of plant cortical microtubule arrays: combining ultrastructure with real-time microtubule dynamicsJOURNAL OF MICROSCOPY, Issue 3 2009D.A. BARTON Summary There are a variety of microscope technologies available to image plant cortical microtubule arrays. These can be applied specifically to investigate direct questions relating to array function, ultrastructure or dynamics. Immunocytochemistry combined with confocal laser scanning microscopy provides low resolution "snapshots" of cortical microtubule arrays at the time of fixation whereas live cell imaging of fluorescent fusion proteins highlights the dynamic characteristics of the arrays. High-resolution scanning electron microscopy provides surface detail about the individual microtubules that form cortical microtubule arrays and can also resolve cellulose microfibrils that form the innermost layer of the cell wall. Transmission electron microscopy of the arrays in cross section can be used to examine links between microtubules and the plasma membrane and, combined with electron tomography, has the potential to provide a complete picture of how individual microtubules are spatially organized within the cortical cytoplasm. Combining these high-resolution imaging techniques with the expression of fluorescent cytoskeletal fusion proteins in live cells using correlative microscopy procedures will usher in an radical change in our understanding of the molecular dynamics that underpin the organization and function of the cytoskeleton. [source] Synthesis and properties of ,-Fe2O3 nanorodsCRYSTAL RESEARCH AND TECHNOLOGY, Issue 9 2010R. Ramesh Abstract We report synthesis of ,-Fe2O3 (hematite) nanorods by reverse micelles method using cetyltrimethyl ammonium bromide (CTAB) as surfactant and calcined at 300 °C. The calcined ,-Fe2O3 nanorods were characterized by X-ray diffraction (XRD), high-resolution scanning electron microscopy (HRSEM), transmission electron microscopy (TEM), energy dispersive spectrometer (EDS), fourier transform infrared spectroscopy (FTIR) and vibrating sample magnetometer (VSM). The result showed that the ,-Fe2O3 nanorods were hexagonal structure. The nanorods have diameter of 30-50 nm and length of 120-150 nm. The weak ferromagnetic behavior was observed with saturation magnetization = 0.6 emu/g, coercive force = 25 Oe and remanant magnetization = 0.03 emu/g. (© 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Sonoelectrochemical Synthesis of Metallic Aluminum NanoparticlesEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 14 2009Chinnathambi Mahendiran Abstract In this paper, we report for the first time on the room-temperature preparation of metallic aluminum nanoparticles by the pulsed sonoelectrochemical method. The prepared nanoparticles were characterized by X-ray diffraction (XRD), high-resolution scanning electron microscopy, transmission electron microscopy (TEM), and high-resolution transmission electron microscopy. TEM analysis shows that the prepared aluminum nanoparticles range from 10 to 20 nm in size. The XRD pattern confirms the formation of metallic aluminum nanoparticles. The results show that the sonoelectrochemical technique is a promising method for the fabrication of air-sensitive metallic nanoparticles that have a high, negative reduction potential.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009) [source] Growth of Cement Hydration Products on Single-Walled Carbon NanotubesJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 6 2009Jonathan M. Makar Single-walled carbon nanotubes (SWCNT) were distributed on the surface of ordinary Portland cement (OPC) grains. The OPC/SWCNT composite was then hydrated at a 0.5 w/c ratio. The effects of the SWCNT on the early hydration process were studied using isothermal conduction calorimetry, high-resolution scanning electron microscopy and thermogravimetric analysis. The observed behavior of the composite samples was compared with both OPC sonicated without SWCNT and previously published data on as-delivered OPC. The SWCNT were found to accelerate the hydration reaction of the C3S in the OPC. The morphology of both the initial C3A and the C3S hydration products were found to be affected by the presence of the SWCNT. In particular, the nanotubes appeared to act as nucleating sites for the C3S hydration products, with the nanotubes becoming rapidly coated with C,S,H. The resulting structures remained on the surface of the cement grains while those in the sonicated and as-delivered OPC samples grew out from the grain surfaces to form typical C,S,H clusters. Classical evidence of reinforcing behavior, in the form of fiber pullout of the SWCNT bundles, was observed by 24 h of hydration. [source] Evolution of Surface Morphology with Introduction of Stacking Faults in ZeolitesCHEMISTRY - A EUROPEAN JOURNAL, Issue 7 2010Neena Abstract This paper sets out to try to determine some of the nanoscopic details of template action in zeolites. The problem has been addressed by monitoring the effects of competitive templating using, in particular, atomic force microscopy and high-resolution scanning electron microscopy. Using these techniques, it is possible to determine the subtle crystal growth changes that occur as a result of altering the concentration of these competitive templating agents. This work concerns the two important intergrowth systems MFI,MEL and FAU,EMT. It was found that some organic templating agents provide much greater structure-directing specificity. So much so in the case of the MFI,MEL system that a 2,mol,% doping with the highly specific tetrapropylammonium cation drastically changes the fundamental growth processes. Furthermore, the effect of template crowding is shown to reduce specificity. This work shows how extensive frustrated intergrowth structures can still be accommodated within a nominal zeolite single crystal. [source] | ||||||||||