The largest database of trusted experimental protocols

X maxn 80 tle

Manufactured by Oxford Instruments

The X-MaxN 80 TLE is a compact energy-dispersive X-ray (EDX) detector designed for use in scanning electron microscopes (SEMs) and other analytical instruments. The core function of the X-MaxN 80 TLE is to detect and analyze the X-rays emitted from a sample when it is exposed to an electron beam, allowing for the identification and quantification of the chemical elements present in the sample.

Automatically generated - may contain errors

2 protocols using x maxn 80 tle

1

Characterization of Conductive Adhesive Composites

Check if the same lab product or an alternative is used in the 5 most similar protocols
The morphologies
of the Cu powder samples and of the top surface of the cured ICA samples
(filler dispersion and microstructure) were characterized using a
Zeiss 1530VP field emission gun scanning electron microscope (FEG-SEM).
Elemental mapping was also conducted within the FEG-SEM using energy-dispersive
X-ray spectroscopy (EDS). Samples of Cu powder and ICAs printed on
glass were attached to carbon adhesive tape mounted on SEM stubs and
coated with a thin layer of gold/palladium (Au/Pd) alloy (80/20) using
a Quorum Q150R S sputter coater. The Au/Pd coating applied was sufficiently
thin to not be recognized in the images. The cross-sectional microstructures
of the ICAs were prepared and characterized using a focused ion beam
(FIB-SEM) system (FEI Nanolab 600 Dual Beam). A platinum (Pt) layer
(∼2 μm thick) was deposited on the surface of the sample
prior to FIB milling to preserve the outermost surface.
A standard
lift-out procedure using FIB-SEM was followed to prepare the lamella
for TEM to achieve a thickness of ∼200 nm. The nanostructure
of the ICA sample sections was then studied using an FEI Tecnai F20
scanning transmission electron microscope (STEM) equipped with Oxford
Instruments energy-dispersive X-ray spectroscopy (EDS) with a windowless
detector (X-MaxN 80 TLE).
+ Open protocol
+ Expand
2

Characterization of Porous Nanocomposite Materials

Check if the same lab product or an alternative is used in the 5 most similar protocols
SEM samples were examined using a Hitachi S-4800 field-emission scanning electron microscope (FE-SEM). High-resolution TEM samples were investigated using a high resolution transmission electron microscope (HR-TEM, STEM, JEOL ARM-200F) having a probe Cs aberration corrector (CEOS GmbH) and an energy-dispersive X-ray spectroscopy (EDS, Oxford Instruments X-MaxN 80 TLE) attached to the TEM. The porous structures of the samples were analyzed in a nitrogen adsorption experiment at −196°C using a BEL BELSORP-Max system. The surface areas and pore sizes of the samples were calculated using the Brunauer-Emmett-Teller (BET) equation and the Barrett-Joyner-Halenda (BJH) method, respectively. Infrared spectra were recorded by a Varian 670-IR spectrometer equipped with an attenuated total reflectance (ATR) device. Nuclear magnetic resonance (NMR) spectra were recorded by an Agilent 400 MHz spectrophotometer using CDCl3 as the solvent and tetramethylsilane (TMS) as the internal standard. A thermal analysis was performed at a heating rate of 5°C min−1 in a nitrogen atmosphere using a thermogravimetric analyzer (TGA, SDT Q600). Isothermal analysis was performed at 250°C. The dissolution of PQ and PQ/CMK-3 in TEGDME was investigated by ultraviolet-visible (UV-VIS) spectroscopy (Varian, Cary 5000).
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!