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Fesem vp scanning electron microscope

Manufactured by Zeiss
Sourced in Germany

The FESEM VP Scanning Electron Microscope is a high-resolution imaging tool designed for materials analysis. It uses a focused beam of electrons to generate detailed images of the surface structure and composition of samples. The FESEM VP provides high-magnification, high-resolution imaging capabilities for a wide range of materials and applications.

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2 protocols using fesem vp scanning electron microscope

1

Nanomaterial Characterization by Advanced Techniques

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The specific surface area and pore distribution were investigated using a Quantachrome Autosorb-IQ porosity equipment (Quantachrome Instruments, Boynton Beach, FL, USA) by Brunauer–Emmett–Teller (BET) and Barrett–Joyner–Halenda (BJH) methods. Prior to analysis, the nanomaterials were degassed at 373–393 K. The morphology of all samples (before and after adsorption) was investigated using a FESEM VP Scanning Electron Microscope (Carl Zeiss, Oberkochen, Germany) at 0.8 nm resolution, 2.5 nm VP mode and 30 kV; also, EDS was applied for the determination of metal content. Functional groups were elucidated using a Cary 630 ATR-FTIR spectrophotometer (Agilent Technologies, Inc., Santa Clara, CA, USA). Prior to analysis, the samples were ground in an agate mortar and dried at 80 °C under vacuum. The FTIR spectra were registered between 4000 and 400 cm−1 (32 scans at a resolution of 8 cm−1 and a threshold of 0.002), and MicroLab Expert v.1.0.0 Software (Agilent Technologies, Inc., Santa Clara, CA, USA) was used for the interpretation.
The elemental analysis was achieved by combustion and pyrolysis coupled with gas chromatography (Flash EA2000, Thermo Scientific, Waltham, MA, USA) [23 (link)].
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2

Nanomaterial Characterization by Advanced Techniques

Check if the same lab product or an alternative is used in the 5 most similar protocols
The specific surface area and pore distribution were investigated using a Quantachrome Autosorb-IQ porosity equipment (Quantachrome Instruments, Boynton Beach, FL, USA) by Brunauer–Emmett–Teller (BET) and Barrett–Joyner–Halenda (BJH) methods. Prior to analysis, the nanomaterials were degassed at 373–393 K. The morphology of all samples (before and after adsorption) was investigated using a FESEM VP Scanning Electron Microscope (Carl Zeiss, Oberkochen, Germany) at 0.8 nm resolution, 2.5 nm VP mode and 30 kV; also, EDS was applied for the determination of metal content. Functional groups were elucidated using a Cary 630 ATR-FTIR spectrophotometer (Agilent Technologies, Inc., Santa Clara, CA, USA). Prior to analysis, the samples were ground in an agate mortar and dried at 80 °C under vacuum. The FTIR spectra were registered between 4000 and 400 cm−1 (32 scans at a resolution of 8 cm−1 and a threshold of 0.002), and MicroLab Expert v.1.0.0 Software (Agilent Technologies, Inc., Santa Clara, CA, USA) was used for the interpretation.
The elemental analysis was achieved by combustion and pyrolysis coupled with gas chromatography (Flash EA2000, Thermo Scientific, Waltham, MA, USA) [23 (link)].
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