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Xl 30 esem tmp scanning electron microscope

Manufactured by Philips

The Philips XL 30 ESEM TMP scanning electron microscope is a laboratory instrument designed for high-resolution imaging and analysis of a wide range of materials. It features an environmental scanning electron microscope (ESEM) configuration, which allows for the examination of samples in a low-vacuum environment without the need for special sample preparation. The microscope is equipped with a tungsten microscope tip (TMP) as the electron source.

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2 protocols using xl 30 esem tmp scanning electron microscope

1

Structural and Optical Characterization of CS/Al-MSN-BZC

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Fourier transform-infrared (FT-IR) measurements were performed on a Bruker VERTEX 70 spectrometer. The FT-IR spectra were recorded in 400 ÷ 4000 cm−1 range with 4 cm−1 resolution. The samples were analyzed from KBr pellets.
The X-ray photoelectron spectroscopy (XPS) spectra were registered on a Thermo Scientific K-Alpha equipment, fully integrated, with an aluminum anode monochromatic source. Charging effects were compensated by a flood gun. Pass energy of 200 eV and 20 eV were used for surgery and high resolution spectra aquisition respectively.
Thermogravimetric analysis (TGA) was done on a Q500 TA Instruments equipment. 2 mg of sample was heated from RT to 700 °C using a heating rate of 10 °C/min under constant nitrogen flow rate.
UV adsorption measurements of BZC were performedat λ = 262 nm on a UV 3600 Shimadzu equipment provided with aquartz cell having a light path of 10 mm.
The morphological characterization of the CS/Al-MSN-BZC composite films was evaluated from the micrograph recorded using a Philips Xl 30 ESEM TMP scanning electron microscope (SEM).
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2

Identifying Efflorescence Compositions via SEM-EDS and XRD

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Efflorescences blooming at fissures were identified using SEM–EDS and XRD. The morphologies of samples on carbon tape were examined using a Philips XL 30 ESEM/TMP scanning electron microscope coupled to an energy-dispersive spectrometer (EDS; EDAX type Sapphire) at the Faculty of Earth Sciences, University of Silesia. Analytical conditions were: accelerating voltage 15 kV, working distance ca 10 mm, and counting time 40 s. In addition, powdered samples were examined using a Bruker AXS D8 ADVANCE diffractometer in the X-Ray Diffraction Laboratory, Institute of Geological Sciences, Polish Academy of Sciences and an X-ray Philips PW 3710 diffractometer at the Faculty of Earth Sciences, University of Silesia. Efflorescence phase compositions are given in Table S2.
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