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Jem 2100 transmission electron microscopy

Manufactured by JEOL
Sourced in Japan

The JEM-2100 is a transmission electron microscope (TEM) manufactured by JEOL. It is designed to provide high-resolution imaging and analysis of a wide range of samples at the nanoscale. The JEM-2100 operates at an accelerating voltage of up to 200 kV and offers advanced features such as a LaB6 electron source, a high-resolution objective lens, and a state-of-the-art digital imaging system. This TEM is a versatile tool that can be used for various applications, including materials science, life science, and nanotechnology research.

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7 protocols using jem 2100 transmission electron microscopy

1

Characterization of PPY Hydrogels and V2O5 Nanowires

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The morphologies of the PPY hydrogels were observed by a SU-70 scanning electron microscopy (Hitachi, Japan) at an accelerating voltage of 20 kV equipped with an energy dispersive X-ray analyzer. The morphology of V2O5 nanowires was observed on JEM-2100 transmission electron microscopy (JEOL, Japan) at 200 kV. Rheology measurements were carried out by using a MCR 302 Rhometer (Anton Paar, Austria). Raman spectra were recorded at room temperature with a MicroRaman System RM3000 spectrometer and an argon ion laser operating at a wavelength of 532 nm as the excitation laser. Thermogravimetric analysis (TGA) was carried out on a STA 449 F3 Jupiter simultaneous thermal analyzer with a heating rate 20 °C min−1 in the air condition. Zeta potential was determined by electrophoretic light scattering (ELS) with Zetaplus (Brookhaven Instruments Corporation, Holtsville, NY, USA). BET surface area was measured by TriStar 3000 specific surface area analyzer.
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2

Biosynthesis of Silver Nanoparticles from Ipomoea oblongifolia Leaves

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I. oblongifolia leaves have been collected from Jazan, Saudi Arabia “16°53′21″N 42°33′40″E”. According to Lubbad et al. (2015) (link), 70% of the methanol extract of I. oblongifolia was obtained. Following the method of Murugan et al. (2016) (link), 5 mL of the extract was used for the biosynthesis of NS by mixing the extract with silver nitrate (AgNO3, 8 × 10-3 M, ~0.06793 gm) in 45 mL of methanol. The reduced NS solution was measured with UV–visible spectroscopy (UV–vis). Then, the type and size of NS are characterized by JEOL JEM-2100 transmission electron microscopy (JEOL Ltd., Tokyo, Japan) (Jiang et al., 2008 ).
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3

Synthesis of Magnetic Nanoparticle Clusters

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Step 1: PVP (0.58 g, molecular weight 58,000) was dissolved in 5 mL ethylene glycol under magnetic stirring. Step 2: DTAB or TTAB or DeTAB (0.02 g) were dissolved in 1 mL pure water, which was then combined with 10 mg individual ferric tetroxide (Fe3O4) nanoparticles in chloroform solution. Step 3: after 3 min vigorous vortex, the mixture in step 2 was transferred into a three-necked flask that was incubated at 40 °C in a water bath, while chloroform was removed in a nitrogen flow (this process takes about 3 min). Step 4: The ethylene glycol solution from step 1 was added into the mixture from step 3 (with a pipette gun, within 15 s) and mechanically stirred for 10 min at a rotation speed of 350 rad·min−1. Then, the resulting mixture was then heated to 80 °C and maintained at that temperature for 6 h. After cooling down to room temperature, the as-formed clusters were divided into two 10 mL centrifuge tubes, washed once with ethanol and centrifuged at 5000 rpm for 15 min to collect the final products that were dispersed in ethanol at a concentration of 20 mg/mL. The morphology of the as-synthesized nanoparticle clusters was characterized with a JEOL JEM-2100 transmission electron microscopy (TEM).
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4

Comprehensive Characterization of GaOOH Nanorods

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The crystal structure of samples was analyzed by a Bruker D8 DISCOVER X-ray diffractometer (XRD). UV-Raman spectra were recorded on a Jobin-Yvon T64000 triple-stage spectrograph with spectral resolution of 2 cm−1. The thermal behavior of the GaOOH nanorod was investigated by thermal gravimetric analyzer (Pyris1 TGA). For the morphological and microstructural analysis, a Hitachi S-4800 field-emission scanning electron microscope (SEM) equipped and a JEOL JEM-2100 transmission electron microscopy (TEM) were utilized. The ultraviolet-visible (UV-vis) absorption spectra were taken using a Hitachi U-3900 UV-vis spectrophotometer. The chemical composition of samples was characterized by a Thermo Scientific K-Alpha X-ray photoelectron spectroscopy (XPS).
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5

Comprehensive Characterization of Nanomaterials

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The transmission electron microscopic (TEM) and high-resolution TEM (HRTEM) images were acquired by a JEM-2100 transmission electron microscopy (JEOL, Tokyo, Japan) at an accelerating voltage of 200 kV. The UV-vis spectra were recorded on a UV-vis absorption spectrophotometer (UV-1800pc) at 800–200 nm. The X-ray photoelectron spectra (XPS) were measured by PHI 500 VersaProbe X-ray photoelectron spectrometer (UlVAC-PHI, Hagisono, Japan). The FT-IR spectra were obtained on an iS10 FT-IR spectrometer at 500–5000 cm−1 (Nicolet, Madison, WI, USA). Zeta potential was recorded on Zetasizer Nano ZS instrument (Malvern, Malvern, UK). The FL spectra were acquired by LS SS Perkin Elmer spectrometer (Perkin Elmer, Waltham, MA, USA) with the slit widths of 4 nm for emission and excitation spectra. All the fluorescence spectra were measured from 330 to 700 nm with a quartz cuvette of 1 cm path length.
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6

Characterization of Fluorescent PAH-Cu NCs

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The fluorescent intensity of PAH-Cu NCs was measured by using a Hitachi F-4500 Fluorescence spectrometer (Tokyo, Japan). The excitation and emission wavelengths were set at 360 and 450 nm, respectively. The slits were set at 10 nm. The UV-visible spectra of each material were measured using a Hitachi U-5100 UV-Visible spectrophotometer (Tokyo, Japan). The pH value of buffer was adjusted using a DKK-TOA pH meter HM-25R (Tokyo, Japan). The X-ray photoelectron spectroscopy (XPS) was determined by ULVAC-PHI PHI 5000 VersaProbe. The transmission electron microscopy (TEM) images of PAH-Cu NCs were obtained by using a JEOL JEM-2100 transmission electron microscopy at a voltage of 200 kV. Fourier transform infrared spectroscopy (FT-IR) spectra of PAH-Cu NCs were measured using a Perkin-Elmer system 2000.
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7

Characterization of Magnetic Nanoparticles

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Ferric chloride hexahydrate (FeCl 3 Raman spectra were collected with the Beda Teck Raman spectrometer (TacticlD). Bacterial DNA extraction kit was used for bacterial DNA extraction (Sangon). Agarose gel electrophoresis of SEA was measured by DYY-6C Electrophoresis system (Bio-Rad). The gel imaging system is Tieneng Gel Imager (Tanon). Transmission electron microscopy (TEM) imaging of AuNP, Au@Ag nanoparticles, and magnetic nanoparticles were performed using JEM-2100 transmission electron microscopy (JEOL Ltd.). A blood blender for magnetic bead attachment to streptavidin was purchased from Xingkang Medical Appliance Co. The zeta potential and dynamic light scattering data of magnetic beads, streptavidin-modified magnetic beads, and streptavidin-modified magnetic beads bound to DNA were measured by a Zetasizer (Nano-Z).
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