Phenom prox desktop
The Phenom ProX Desktop is a compact, user-friendly scanning electron microscope (SEM) designed for high-resolution imaging and analysis of a wide range of samples. It offers a simple and intuitive interface, automated functions, and advanced imaging capabilities.
Lab products found in correlation
8 protocols using phenom prox desktop
Characterization of Metallic Powders
SEM Analysis of Impact Fracture Surfaces
impact fractured sample break surfaces were obtained using a Phenom
ProX Desktop from Phenom-World BV (Eindhoven, Netherlands). Charging
was minimized by a Cressington 108 sputter coater (Watford, England)
to apply a thin gold coating on the fractured surface of the impact
bars, with a sputter duration of 10 s. The accelerating voltage of
the SEM was set to 10 kV, and the samples were examined at a magnification
of 1000×.
Ultrastructural Analysis of Extracellular Matrix
Scanning Electron Microscopy of Polyurethane Scaffolds
Characterization of Multifunctional Materials
FT-IR spectra were obtained with Bruker Alpha in the wave number range of 400 and 4000 cm−1 (Milan, Italy). SEM analyses were performed with Phenom Pro X Desktop (Thermo Fisher Scientific, Rome, Italy).
The rheological tests were carried out using a DHR-2 TA Instrument rotational rheometer (TA Instruments-Waters S.p.A., Sesto San Giovanni, Italy).
UV measurements were performed using an Eppendorf AF2200 spectrophotometer (Milan, Italy).
Cell cultures were performed using an Eppendorf New Brunswik S41i incubator (Milan, Italy).
Fluorescence images were obtained with an AxioVert200 (Zeiss) microscope (Milan, Italy).
A 3D printer Zmorph (Wroclaw, Poland) connected with a pressure controller OB1 working at pressures of 0–8000 mbar from Elveflow (Paris, France) was used to test printability of the inks.
Surface Morphology Analysis of PVC/SEBS Blends
Surface Defects in Extruded Filaments
The scope of the analysis was to investigate the presence of surface defects caused by prolonged residence times, or by the presence of solid particles in the metering section. The selected frequencies were 0.5, 5 and 20 rpm, based on model screening, allowing us to identify the position of the point of melt finalization. Two filament samples were always collected from the extrusion under steady state conditions, at a 15 min interval. The process was repeated using 2 nozzles with 0.8 and 1.5 mm final opening diameter, for a total of 12 samples.
Ultrastructural Analysis of ZIKV-Infected Monocytes
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