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Em 90

Manufactured by Zeiss
Sourced in Germany

The EM-90 is an electron microscope designed and manufactured by Zeiss. It is a versatile tool for high-resolution imaging and analysis of a wide range of materials and samples. The EM-90 provides advanced imaging capabilities, allowing users to study the detailed structure and composition of their specimens.

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3 protocols using em 90

1

Comprehensive Characterization of Ilmenite and TiO2 Nanoparticles

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Characterization of raw ilmenite and titanium dioxide nano particles (TiO2 NPs) were carried out by using different analytical techniques such as transmission electron microscopy (TEM) using a Zeiss EM-90 operating at 80 kV tension. Scanning Electron Microscope (SEM) Model Jeol 6510 JSM, LA. Brunauer–Emmett–Teller (BET) by using N2 adsorption/desorption at 77 K using an automatic surface area device (BELSORP MINI X). X-ray diffraction (XRD) (Paralytical Philips APD-3720, Netherlands) with Cu–kα radiation (λ = 0.154 cm−1) and operated at 40 kV, 35 mA, 5 min scanning speed in the 2θ range of 5°–80°. Fourier transform infrared (FTIR) spectrum of TiO2 NPs was recorded in the range of 400–4000 cm−1 with a Bruker FT/IR-2000 spectrometer. X-ray fluorescence (XRF) technique using Axios MAX, PAN analytical, 40 kV, 50 Ma.
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2

Synthesis and Characterization of TiO2 Nanoparticles

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All chemicals and solvents were purchased from Merck and Sigma-Aldrich (Germany) and used without further purification. A Win-Bomem spectrometer, version 3.04 Galactic Industries Corporation over the range of 400–4000 cm−1 was used to obtain Fourier transform infrared (FT-IR) spectra. The synthesized TiO2 NPs were coated with a thin layer of gold and visualized using a scanning electron microscopy/energy dispersive X-ray spectroscopy (SEM/EDX) instrument, VWGA3 TESCAN (20.0 KV). For recording the Transmission electron microscopy (TEM) images, so-called TiO2 NPs were dispersed in distilled water and used a Zeiss EM-90 operating at 80 kV tension. Wide angle X-ray diffraction (XRD) profiles of TiO2 NPs were collected by using a Bruker D8 Advance diffractometer with wavelength, λ = 0.154059 nm (Cu Kα) at 30 keV.
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3

Glycocalyx Preservation in Brain Tissue

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The animals were perfused through the abdominal aorta with a solution containing 2.5% glutaraldehyde, 2% paraformaldehyde, and 2% lanthanum nitrate, as described by Vogel et al. [27] , to preserve the glycocalyx in brain tissues. After the brain tissues were embedded in epon resin and 120-nm sections were contrast-enhanced with 5% uranyl acetate in deionized water for 20 min and a solution containing 120 mmol/L sodium citrate, 80 mmol/L lead citrate and 160 mmol/L sodium for 2 min, the glycocalyx was photographed using a transmission electron microscope (EM 90; Zeiss, Oberkochen, Germany).
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