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Vega 3 electron microscope

Manufactured by TESCAN
Sourced in Czechia, United Kingdom

The VEGA 3 is a versatile electron microscope designed for high-resolution imaging and analysis. It features a tungsten or LaB6 electron source, providing stable and reliable performance. The VEGA 3 offers a wide range of magnification capabilities, allowing users to explore samples at the micro- and nanoscale levels. The instrument is equipped with various detectors to capture different types of signals, enabling comprehensive characterization of the sample.

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5 protocols using vega 3 electron microscope

1

Characterization of Porous Materials

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Specific surface area, pore volume and pore size distribution were investigated using Quantachrome Nova 1200e by nitrogen adsorption at 77 K and analyzed by the BET and BJH equations. Prior to analysis, all samples were degassed at room temperature for 48 hours. The samples for transmission electron microscopy (TEM) were obtained by dispersing a small probe in ethanol to form a homogeneous suspension. Then, a suspension drop was coated on a copper mesh covered with carbon for a TEM analysis (FEI TECNAI G2 F20, at an operating voltage of 200 kV). To analyze the samples using high-resolution scanning electron microscopy (SEM), the obtained ground xerogel was deposited on a metal tip and investigated without additional spraying using a Magellan 400 L ultra-high resolution electron microscope. To analyze plasma clot using SEM, the obtained samples were dried under vacuum for 1 hour and investigated without additional spraying using a TESCAN VEGA 3 electron microscope. Optical microscopy was done on a LOMO MIKMED 6 microscope with an X10 lens. Hydrodynamic diameter was measured by the DLS technique on Photocor Compact Z. Spectrophotometrical measurements of enzymatic activity were carried out using an Agilent Cary HP 8454 Diode Array spectrophotometer with TEC.
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2

Scanning Electron Microscopy of Freeze-Dried Samples

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SC samples were frozen overnight at −80°C and then lyophilized for 24 h. The freeze‐dried products were mounted on sample stubs and sputter‐coated with gold, and images were acquired on a scanning VEGA3 electron microscope (Tescan, Brno, Czech Republic).
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3

Characterization of Nanomaterial Crystallinity

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The crystal phase and crystallinity of the samples were studied by the X-ray diffraction method (Rigaku SmartLab 3 diffractometer of the Engineering center of the Saint-Petersburg State Technological Institute (Technical University)) using Cu-Kα irradiation (λ = 1.54 Å), with samples being scanned along 2θ in the range of 5–80° at a speed of 0.5°/min. For XRD analysis, the samples were dried at 120 °C for 4 h. The particle size and zeta potential of NPs were measured using a Photocor Compact Z. For SEM analysis, the samples were dried in vacuo for 1 h and then examined using a Tescan VEGA 3 electron microscope. The FTIR spectra were obtained by Nicolet iS5 spectrometer. The samples were dried in oven at 60 °C overnight, powdered with agate mortar, and then embedded in mineral oil for measurement.
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4

Scanning Electron Microscopy of Biscuit Microstructure

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The Vega3 electron microscope (SEM) (TESCAN) was used to evaluate the biscuit samples' surface microstructure. In this regard, the small parts of the dried biscuits were attached to aluminum stubs by double‐sided adhesive tape. Then, a thin layer of gold was coated over the samples using Desk Sputter Coater DSR1, Nanostructural Coating Co. The accelerating voltage and temperature used in the test were 10 kV and 25°C, respectively (Gahruie et al., 2020 (link)).
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5

Elemental Composition Analysis of Hydrophobic Fabrics

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Qualitative and quantitative elemental composition analyses were performed to identify the types of water-repellent finishes. The tests were performed on the face side (fabric with hydrophobic finish).
The analyses were performed on an INCA Energy EDS X-ray microanalyzer from Oxford Instruments Analytical (Oxford, UK), coupled with a VEGA3 electron microscope from TESCAN (Brno, Czech Republic), equipped with a monocrystalline lithium (Li)-activated silicon detector, enabling the detection of elements from beryllium (Be) to uranium (U), with a maximum resolution of 128 eV for the Mn (Kα) line. X-ray microanalysis of the surface of fabrics with hydrophobic finishes was carried out under low-vacuum, at a pressure of 30 Pa, using an electron beam energy of 20 kV, without spraying the samples with a conductive substance, at a magnification of 300×. Qualitative and quantitative analyses of the chemical composition were carried out from areas of 0.5 mm2 in triplicate. The values of percentages of elements were determined by INCA program. The results of weight percentages of individual elements are given with an accuracy of 0.01%.
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