Specimen Discs for Large-Scale Handling of Preparations Used in Scanning Electron Microscopy

1972 ◽  
Vol 47 (4) ◽  
pp. 214-215
Author(s):  
Donald D. Thompson ◽  
James A. Esterly
2018 ◽  
Vol 773 ◽  
pp. 287-291
Author(s):  
Eui Soo Kim

High-pressure gas containers must be able to withstand high internal pressures because they store compressed gases. Otherwise, cracks or defects may lead to an explosion, which may in turn lead to a large-scale disaster. Therefore, accurate analysis of the causes of cracks or defects and various techniques for detecting cracks or defects are needed. In this research, we analyzed the failure mechanism of a high-pressure gas container through fractography using scanning electron microscopy and optical microscopy and through measurements of their mechanical and chemical properties.


2017 ◽  
Author(s):  
Yusuke Hirabayashi ◽  
Juan Carlos Tapia ◽  
Franck Polleux

A challenging aspect of neuroscience revolves around mapping the synaptic connections within neural circuits (connectomics) over scales spanning several orders of magnitude (nanometers to meters). Despite significant improvements in serial section electron microscopy (SSEM) technologies, several major roadblocks have impaired its general applicability to mammalian neural circuits. In the present study, we introduce a new approach that circumvents these roadblocks by adapting a genetically-encoded ascorbate peroxidase (APEX2) as a fusion protein to a membrane-targeted fluorescent reporter (CAAX-Venus), and introduce it in single pyramidal neurons in vivo using extremely sparse in utero cortical electroporation (IUCE). This approach allows to perform Correlated Light-SSEM (CoLSSEM) on individual neurons, reconstructing their dendritic and axonal arborization in a targeted way via combination of high-resolution confocal microscopy, and subsequently imaging of its ultrastuctural features and synaptic connections with the ATUM-SEM (automated tape-collecting ultramicrotome - scanning electron microscopy) technology. Our method significantly improves the the feasibility of large-scale reconstructions of neurons within a circuit, and bridges the description of ultrastructural features of genetically-identified neurons with their functional and/or structural connectivity, one of the main goal of connectomics.


2021 ◽  
Vol 22 (3) ◽  
pp. 595-601
Author(s):  
R.G. Abaszade ◽  
S.A. Mamedova ◽  
F.G. Agayev ◽  
S.I. Budzulyak ◽  
O.A. Kapush ◽  
...  

We have synthesized large scale, thin, transparent graphene oxide (GO) flakes by Hummer’s method and investigated their suitability for fabrication of transparent nanocomposites. The GO flakes were comprehensively characterized by X-ray diffraction, Scanning Electron Microscopy (SEM), Energy Dispersive X-ray analysis (EDX), Raman spectroscopy and Differential Scanning Calorimetry (DSC). X-ray diffraction displayed the peak of graphene oxide at 9°degree, which is characteristic peak of GO in agreement with the literature results. Scanning Electron Microscopy images revealed that thin, transparent, flake form GO with 14,8 µm lateral size and 0,31µm thickness were synthesized. The comparison with literature results show that for the first time, our group could synthesize large scale, thin and more transparent GO flakes by simple Hummer’s method using simple dispersed graphite. EDX measurements indicate the formation of layered structure with oxygen containing functional groups. The intensity ratio between D and G peaks in the Raman spectra proves that less defective GO flakes have been synthesized. The solution ability of the synthesized material indicate that high quality GO flakes were synthesized, which make them effective soluble material due to oxygen containing groups formed on the graphene plane during synthesis process.DSC results shows that these flakes are thermally stable till 200°C.  Due to high solubility properties, large scale and transparency they can be very useful in fabrication of high optical transparent nanocompoties for replacement indium tin oxide transparent conductors in solar panels, biomedical applications and microwave absorbers for electromagnetic interference (EMI) environmental protection.


2020 ◽  
Vol 31 (8) ◽  
pp. 1367-1384 ◽  
Author(s):  
C Karthikeyan ◽  
R Dhilip Kumar ◽  
J Anandha Raj ◽  
S Karuppuchamy

Metal sulfides received key interest as an electrode material for storage and conversion of energy. Here, the novel nanostructured N17S18 and (CoNi)3S4 materials were synthesized via one-step hydrothermal method, and the synergistic effect of metal ions and electrochemical properties was investigated. A new and simple solution growth technique was employed in this work. The prepared nanopowders were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, field emission scanning electron microscopy, energy-dispersive X-ray spectroscopy techniques. The X-ray diffraction analysis of the prepared nanopowder revealed the formation of cubic phase cobalt nickel sulfides (CoNi)3S4 and hexagonal phase nickel sulfides (Ni17S18). Scanning electron microscopy analysis display fibrous, flakes and sheet-like morphology for CoxSx, N17S18 and (CoNi)3S4, respectively. Fibrous and sheet-like morphology exhibits higher electrochemical performance in supercapacitors. The electrochemical behavior of the amorphous CoxSx, crystallite Ni17S18 and (CoNi)3S4 modified electrodes was investigated using electrochemical impedance spectroscopy, cyclic voltammetry and galvanostatic charge–discharge techniques. The specific capacitance of 57 F/g and 31 F/g were obtained for the amorphous CoxSx and crystalline (CoNi)3S4 powder, respectively. Amorphous CoxSx modified electrode retains 76% of initial capacitance after 1000 repeated cycling process. These results of this study suggest that the CoxSx and crystalline (CoNi)3S4 are appropriate materials for supercapacitor applications.


2007 ◽  
Vol 121-123 ◽  
pp. 209-214 ◽  
Author(s):  
Zai Yin Huang

Large-scale synthesis of In-doped SnO2 (ITO) nanowires was achieved by direct thermal evaporation of a mixture of Sn and In powders at 900°C in an Argon atmosphere. Scanning electron microscopy and transmission electron microscopy observations show that ITO nanowires have diameter ranging from 20 to 100 nm and lengths up to several tens of micrometers. By altered the reaction temperature, we find that the temperature of the reaction is the critical factor for the morphologies and sizes of the ITO nanowires.


2009 ◽  
Vol 79-82 ◽  
pp. 373-376 ◽  
Author(s):  
Zhao Deng ◽  
Ying Dai ◽  
Hai Rui Liu ◽  
Wen Chen

Large scale BaTiO3 nanorods were successfully synthesized by a template method based on a precipitation process. The templates used in our method are H2Ti8O17 nanorods, which can be synthesized from K2Ti4O9 fibers. The unique process of the synthesis is BaC2O4•0.5H2O shell was coated on the 1-dimensional H2Ti8O17 nanorods (the core). The as-prepared products were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The results show that the BaTiO3 nanorods are ~100-300 nm in diameter and ~2-10 m in length. The process described provides a general route to fabricate this kind of perovskite 1-dimensional nanostructures, such as SrTiO3 and PbTiO3.


2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Bharat G. Pawar ◽  
Dipak V. Pinjari ◽  
Sanjay S. Kolekar ◽  
Aniruddha B. Pandit ◽  
Sung H. Han

In this communication we report the rapid nanostructure of SnO2 with a spherical morphology which has been prepared in large scale via sol-gel method. The products were characterized with scanning electron microscopy, X-ray powder diffraction, transmission electron microscopy, FTIR, and photoluminescence spectroscopy. The strong photoluminescence of the nanosphere in visible region suggested possible application in nanoscaled optoelectronic devices. A possible growth mechanism for the SnO2 nanosphere in terms of solvation, hydrolysis, and polymerization was proposed.


Minerals ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 354
Author(s):  
Jim Buckman ◽  
Anabel Aboussou ◽  
Onoriode Esegbue ◽  
Thomas Wagner ◽  
Gabriele Gambacorta

Mudrocks are highly heterogeneous in terms of both composition and fabric, with heterogeneities occurring at the submicron to centimetre plus scale. Such heterogeneities are relatively easy to visualise at the micron-scale through the use of modern scanning electron microscopy (SEM) techniques, but due to their inherent fine grain size, can be difficult to place within the greater context of the mudrock as a whole, or to visualise variation when viewed at a centimetre scale. The utilisation of SEM to collect automated high-resolution backscattered (BSE) images (tiles) over whole, polished thin-sections presents a potential large data bank on compositional and fabric changes that can be further processed using simple image analysis techniques to extract data on compositional variation. This can then be plotted graphically in 2D as colour contoured distribution maps to illustrate any observed variability. This method enables the easy visualisation of micron-scale heterogeneity present in mudrock, which are here illustrated and discussed for pyrite and organic content at the larger (thin-section) centimetre scale. This does not require the use of other techniques such as energy dispersive x-ray (EDX) mapping to identify phases present, but instead utilizes BSE images that may already have been collected for textural fabric studies. The technique can also be applied to other phases in mudrocks, such as carbonates and silicates, as well as porosity. Data can also be extracted and used in a similar fashion to bulk compositional analytical techniques such as inductively coupled plasma-atomic emission microscopy (ICP-AES) and carbon, nitrogen and sulphur (CNS) analysis, for average organic carbon and percentage pyrite.


Author(s):  
P.S. Porter ◽  
T. Aoyagi ◽  
R. Matta

Using standard techniques of scanning electron microscopy (SEM), over 1000 human hair defects have been studied. In several of the defects, the pathogenesis of the abnormality has been clarified using these techniques. It is the purpose of this paper to present several distinct morphologic abnormalities of hair and to discuss their pathogenesis as elucidated through techniques of scanning electron microscopy.


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