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Phenom prox scanning electron microscope

Manufactured by Thermo Fisher Scientific
Sourced in United States

The Phenom ProX is a scanning electron microscope (SEM) designed for high-resolution imaging and analysis of materials. It offers a compact and user-friendly design, providing a versatile tool for researchers and technicians in various fields, including materials science, nanotechnology, and life sciences.

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8 protocols using phenom prox scanning electron microscope

1

Characterization of Silver Nanoparticles

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XRD analysis was used to investigate the crystallinity of AgNPs, using Bruker D2 Phaser Diffractometer with cupper tube (KαCu = 0.15418 nm), in range of the 5°–70°, with acceleration tension and applied current of 30 kV, and 30 mA, respectively. FTIR was used to identify the functional group using a Perkim Elmer spectrometer (Spectrum One model) at transmittance mode operation at range of 4000–450 cm−1, with 4 cm−1 resolution and 32 runs. Scanning Electron Microscopy coupled to Energy Dispersive Spectroscopy (SEM–EDS) was used to verify the morphology of the AgNPs using Phenom Prox Scanning Electron Microscope (Thermo Fisher Scientific model), operating at 15 kV voltage and 100 µm of amplitude with around 2550 × magnification. Dynamic light scattering (DLS) was used to evaluate the diameter of the AgNPs-KV using NanoBrook Omni equipment (Brookhaven Instrument Corporation, New York) equipped with red laser diode (35 mV, λ = 640 nm) at detection angle of 90°. Moreover, the procedure was carried out in triplicates by using BIC Dynamic Light Scattering Particles Sizing Software, version 1.2.1.0 (USA).
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2

Topographical and Chemical Characterization of Implant Surfaces

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Under a Captair Flow 468 ISO5 laminar flow hood (AirLab), the overall topography of REF and TEST implants was qualitatively examined using a Phenom ProX Scanning Electron Microscope (ThermoFisher scientific). Micrographs at different magnifications were observed to assess the topographies at different scales. Then, surface chemical composition was assessed by Energy Dispersive X-Ray Spectrometry (EDX). Next, roughness measurements were conducted on an Altisurf 3D profilometer (Altimet). Areas of 200×750µm for the interspaces of threads were evaluated in both coronal and apical areas. The arithmetic mean deviation (Sa), root-mean-square deviation (Sq), maximum peak-to-valley height (Sz) and developed interfacial area ratio (Sdr) of the surface were extracted, constituting the main roughness parameters. Three REF and TEST implants were examined and measurements were performed in triplicate. Finally, REF and TEST surfaces were reproduced on cpTi discs to assess implant surface energy. Wettability was tested through contact angle measurements on a DSA25 tensiometer (Krüss). Surface free energy was assessed using the Owens-Rankine formulation, with three liquids, droplets of 2µl, and ten contact angle measurements per liquid.
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3

Scanning Electron Microscopy Imaging

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SEM was carried out with a Phenom ProX scanning electron microscope (Thermo Fisher Scientific, MA, USA). A small amount of powder was mounted on 12 mm stubs with carbon tabs (Agar Scientific, UK) and coated with gold by a Q150S rotary-pumped sputter coater-carbon coater (Quorum, UK). Imaging was carried out at an accelerating voltage of 5 kV at magnifications 175-2900 and 10 kV at magnifications 4300-29000.
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4

Cheese Microstructure Analysis

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The cheese samples (approximately 1 mm × 20 mm) were stored at a temperature of -80 • C. Then, they underwent a drying process using a lyophilizer. Later they were coated in gold with a DV-TSC metallizer (Denton Vacuum LLC, Moorestown, NJ, USA) to be observed in a Phenom Pro X Scanning Electron Microscope (Phenom-World, Thermo Fisher Scientific, Waltham, MA, USA) operated at 10 kV. The fields were randomly selected over the sample area. The images were recorded at 4500× magnification and were used to determine the average pore size using ImageJ v.1.43s software (National Institute of Health, Bethesda, MD, USA).
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5

Phase Identification and Microstructural Analysis of FeCoCrNi and FeCoCrNiMo High-Entropy Alloy Coatings

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The FeCoCrNi and FeCoCrNiMo0.2 high-entropy alloy coatings were cut into 10 mm × 10 mm × 8 mm samples, which were ground with 240 #, 600 #, 800 #, 1000 # and 1200 # sandpapers, respectively, and finally polished. The phase identification of the samples was carried out by an AL-2700B X-ray diffractometer (Dandong Aolong Radiative Instrument Co., Ltd., Dandong, China). The test parameters are as follows: the target is Cu, the scanning range (2θ) is 10°~90°, the scanning speed is 5°/min, the tube voltage is 40 kV and the tube current is 30 mA. After etched with aqua regia solution, the cross-sectional morphology and chemical composition of the coatings were analyzed by a Phenom proX scanning electron microscope (Phenom-World, Eindhoven, The Netherlands) and energy dispersive spectrometer (EDS).
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6

Sputter Coating for SEM Imaging

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Before starting with SEM observation, a Desk Sputter Coater (Phenom-World B.V., Eindhoven, The Netherlands) was used to sputter the samples with gold (150 A).
A Phenom ProX scanning electron microscope (Phenom-World B.V., The Netherlands) was used to characterize all samples at microscale and to visualize the biofilm formation on the discs.
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7

Laser-Assisted Biogel Transfer onto Titanium Thin Films

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Glass slides (Menzel Glaser, Braunschweig, Germany) (26 mm × 76 mm × 1 mm) were used as the donor substrate, on the surface of which Ti was deposited by magnetron sputtering using a VSE-PDV-DESK-PRO installation (OOO Vacuum Systems and Electronics, Novosibirsk, Russia). The film surface was studied by atomic force microscopy on a Solver Pro M complex (ZAO Nanotechnology MDT, Moscow, Russia) in order to determine the thickness of the Ti film, which was 50 ± 10 nm.
Immediately prior to laser transfer, a layer of empty gel or gel mixed with yeast was deposited on the surface of the Ti film of the donor substrate (200-μm thick). The gel was an aqueous solution of 2% hyaluronic acid (Mw = 70 kDa, Contipro Pharma, Dolní Dobrouč, Czech Republic).
Opposite the donor substrate with the gel, a 12-well plate (Costar Corning, Corning, NY, USA) was placed and fixed on an automated moving platform. For visual control of the process of formation and the transfer of the gel jets and drops, a Fastcam SA-3 high-speed camera (Photron, Tokyo, Japan) with frontal illumination from a continuous laser with a wavelength of 630 nm was used. After laser exposure, the Ti films were examined using a PHENOM ProX scanning electron microscope (Phenom-World, Eindhoven, The Netherlands) and an HRM-300 Series optical 3D microscope (Huvitz, Anyang-si, Gyeonggi-do, Korea).
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8

Disinfectant Impact on Tensile Specimen Fracture

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The tensile specimens were immersed in disinfectant until saturation. Methylene blue was added in the solution for evaluating the fluid penetration depth by observing the coloring of the fracture surfaces. Specimens were tested using an Instron 8872 Universal Test Machine (Instron Inc., Kawasaki, Japan) equipped with a load cell of 25 kN. The testing speed was set at a rate of 1 mm/min and the extensometer gauge length was 25 mm.
Phenom ProX scanning electron microscope (SEM) (Phenom World, Eindhoven, The Netherlands) was used for investigating if the specimens fracture surfaces show any specific features which might be caused by the disinfectant action.
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