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145 protocols using jsm 6500f

1

Comprehensive Characterization of LZ Samples

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Top-view visual observation and field emission scanning electron microscopy (FE-SEM, JEOL JSM-6500F, Japan) were used to observe the surface morphology and cell adhesion morphology of the LZ samples. Energy-dispersive X-ray spectrometry (EDS, JEOL JSM-6500F, Japan) and X-ray diffraction (XRD, D8 DISCOVER - Bruker) were respectively used to identify surface element composition and chemical composition. Surface roughness was measured using a white-light interferometer (Filmetrics® Profilm3D® Optical Profilometer, KLA, United States).
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2

Surface Characterization Using FE-SEM

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For surface analyses using SEM, a field emission scanning electron microscope (FE-SEM) (JSM-6500FS, JEOL, Tokyo, Japan) was used under the following settings: accelerating voltage: 25 kV, irradiation current: 1000 nA, and scanning range: ×500. Elemental analysis was conducted using this FE-SEM. Furthermore, EDS analysis (JSM-6500FS, JEOL) was performed with a sampling time of 30 s.
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3

Comprehensive Metallographic Analysis of Samples

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The samples were ground and polished. Optical imaging was performed using an Microphot FXA (Nikon, Tokyo, Japan) optical microscope equipped with an Olympus DP73 camera (Olympus, Hamburg, Germany) and the Stream Motion Programme. Further metallographic analyses were performed using a scanning electron microscope with a ZEISS-Crossbeam 550/EDAX (Carl Zeiss AG, Oberkochen, Germany) instrument for the FE-SEM/BSE/EDS. In addition, a JEOL JSM-6500F (JEOL Ltd., Tokyo, Japan) scanning electron microscope was used for certain FE-SEM/EDS analyses. Where necessary, etching with the aqua regia etchant (10 mL HNO3 + 30 mL HCl + 20 mL glycerine) was applied.
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4

Metallographic Characterization of Fe-6.5wt%Si

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Metallographic analyses FE-SEM/EDS were performed using a scanning electron microscope JEOL JSM-6500F (JEOL Ltd., Tokyo, Japan). FE-SEM/EDS analyses of the powder particles were performed at an accelerating voltage of 15 kV.
Optical imaging was performed using a ZEISS Axio Imager Z2M (Carl Zeiss AG, Oberkochen, Germany) optical microscope.
Samples under investigation were randomly selected powder particles and metallographic cross-sections of the DSC-remelted bulk samples of Fe-6.5wt%Si.
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5

Synthesis and Characterization of UiO68CCG and IR15CCG

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UiO68CCG and IR15CCG were synthesized via a previously published process [28 (link)]. Other reagents and solvents were purchased from commercial sources and used without further purification. All experiments were carried out in the ambient atmosphere, unless otherwise mentioned. Powder X-ray diffraction (XRD) patterns were obtained using a Bruker AXS D8 ADVANCE (Bruker Corporation, Billerica, MA, USA). Field emission scanning electron microscope (FE-SEM) observations and energy dispersive X-ray spectrometry (EDX) analyses were carried out via a JEOL JSM-6500F (JEOL Ltd., Akishima, Japan). Transmission electron microscope (TEM) observations and selected area electron diffraction (SAED) analyses were carried out on a JEOL JEM-2010 (JEOL Ltd., Akishima, Japan). Fourier transform infrared (FT-IR) spectra were recorded on a JASCO FT/IR-4100 spectrometer (JASCO Corporation, Hachioji, Japan). Inductively coupled plasma atomic emission spectroscopy (ICP-AES) was carried out by a Shimadzu ICPE-9000 instrument (Shimadzu Corporation, Kyoto, Japan).
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6

Morphological Analysis of Sintered Porous Al

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The morphology of the as-received starting powders, PMMA particles, the elemental powder mixture and the final powder mixture was observed using scanning electron microscope (SEM, Jeol JSM6500F, JEOL Ltd., Tokyo, Japan). For the microscopic examination of the sintered porous Al, the cross-section of the specimen was prepared. The microstructure and pore morphology of the specimen cross-section were then viewed by SEM.
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7

Longitudinal SEM Analysis of 3DP Structures

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3DP structures were sectioned longitudinally to facilitate observation of the internal architecture and morphology using field emission scanning electron microscope (SEM) (JEOL JSM-6500F, JEOL Ltd., Japan) at an operating voltage of 5 keV. Each structure was mounted on an aluminium stub using a cold cure resin (Extec Corp, Enfield, CT 06083-1258, US), allowed to cure for 24 ± 2 h and subsequently gold-coated using a sputter chamber prior to SEM examination.
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8

3D Printed Structure Characterization

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3DP structures were also sectioned longitudinally by a blade to facilitate observation of the internal architecture and morphology using field emission SEM (JEOL JSM-6500F, JEOL Ltd., Japan) at an operating voltage of 5 keV. The surfaces of the 3DP structures post-fracture were also analysed using SEM. Each 3DP structure was mounted on aluminium stubs using a cold cure resin (Extec Corp, Enfield, CT 06083-1258, USA), allowed to cure for 24 ± 2 h and subsequently gold-coated using a sputter chamber prior to SEM examination.
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9

Characterization of Starch Granule Morphology

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The morphology and particle size of the starch granules was investigated using scanning electron microscopy. Powder starch samples were evenly sprinkled on double sided adhesive tape and were attached to a circular specimen aluminum stub. The samples were coated with a 10 nm thick coating of gold using gold sputter coater (Desk II, Denton Vacuum). Photomicrographs were taken by Field Emission Scanning Electron Microscope (JSM-6500F, JEOL Ltd., Japan) using 5.0 kV of accelerated voltage and a 10 mm of working distance. The size of starch granules were estimated using Image J, image analyzer, software. Randomly, thirty granules were selected and their length and width were measured from the micrographs.
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10

Comprehensive Characterization of Catalysts

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The chemical compositions were characterized by X-ray photoelectron spectroscopy (XPS) (ESCALAB 250). The crystal structure of phases of each sample was determined by using the X-ray diffraction instrument (XRD) (XRD-7000S Shimadzu). The field-emission scanning electron microscopy (FE-SEM, JSM 6500F, JEOL) and transmitted electron microscopy (TEM) (FEG TEM technai G2 F30) instruments were used for morphology characterizations. The Shimadzu 3600 Plus UV-vis spectrophotometer was used to check absorption properties of the catalysts and the concentration of the pollutant.
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